WATER TREATMENT

Abstract

Methods and systems for in situ electrochemical treatment of aqueous solutions used in agricultural systems, community systems and industrial systems. In aspects, is an in situ electrochemical method for the treatment of fertigation water, comprising: flowing the fertigation water through an electrochemical cell comprising at least one anode and at least one complementary cathode while simultaneously adjusting one or more of current density, flow rate and pH, wherein said flowing fertigation water contacts the anode and cathode causing one or more of: degradation of a recalcitrant organic contaminant, mineralization and solubilization of an organic, forming a disinfection agent against a pathogen, and maintaining nutrient levels in said fertigation water; and collecting treated effluent.

Claims

1.-114. (canceled)

115. A regenerative in situ oxidant producing method for the treatment of fertigation water, comprising: flowing fertigation water containing organic matter through an electrochemical cell to effect regenerative mediated electrolysis, the electrochemical cell comprising a boron doped diamond (BDD) anode and at least one complementary stainless steel cathode while simultaneously adjusting one or more of current density, flow rate and pH, continuously regenerating oxidative species in an effective amount to control an oxidant susceptible pathogen and/or degrade the organic matter releasing solubilized nutrients in said fertigation water; and collecting the treated effluent.

116. The method of claim 115, wherein the reactive oxygen species selected from O.sub.2, O.sub.3, H.sub.2O.sub.2 and OH.

117. The method of claim 116, wherein macronutrient content of the fertigation water remains substantially unaltered during treatment.

118. The method of claim 115, wherein said treatment mineralizes and solubilizes organic matter increasing nutrient levels comprising ammonium ions and nitrate.

119. The method of claim 115, wherein: chlorate species formed in said fertigation water is below acceptable levels of below about 2 mg/L in said treated effluent; and/or ammonium, nitrate and sulphate ions are increased in said treated fertigation water.

120. The method of claim 115, wherein: (a) the current density is at least about 0.76 mA/cm.sup.2 to about 9.09 mA/cm.sup.2, about 1.14 mA/cm.sup.2, about 2.27 mA/cm.sup.2, about 3.41 mA/cm.sup.2, about 4.55 mA/cm.sup.2, about 6.82 mA/cm.sup.2 or about 9.09 mA/cm.sup.2; and/or (b) the pH of the fertigation water during treatment is at least about 5.4, about 5.4 to about 8.5 or about 5.5 to 6.5, wherein the pH is selected to be favorable for chloride and nitrogen species in said fertigation water; and/or (c) the flow rate is selected to provide a residence time during treatment of up to about 5, 10, 15, 20, 25 or 30 minutes;

121. The method of claim 115, wherein the method is conducted at about room temperature and/or conducted under ambient light.

122. The method of claim 115, wherein the oxidant-susceptible pathogen is selected from fungi, bacteria, viruses, oocymetes, and mycoplasmas.

123. The method of claim 115, wherein said fertigation water is derived from a municipal water source or an industrial water source.

124. The method of claim 115, wherein the fertigation water comprises organic waste, compost, guano, sewage, manure, bone meal, soya meal, kelp extract, plant leaves, plant roots, wood debris and combinations thereof.

125. The method of claim 115, further comprising re-using the treated effluent and re-treating said re-used effluent.

126. The method of claim 115, wherein said treatment degrades a recalcitrant organic contaminant in said fertigation water.

127. The method of claim 115, wherein said treated effluent comprises one or more of stable levels of oxidative species, increased stable nutrient levels, mineralized organic, and safe chlorate species levels.

128. A regenerative in situ oxidant generating method for the treatment of fertigation water, comprising: flowing fertigation water containing organic species through an electrochemical cell to effect regenerative mediate electrolysis, the electrochemical cell comprising at least one anode and at least one complementary cathode while simultaneously adjusting one or more of current density, flow rate and pH, wherein said flowing of said fertigation water continuously regenerates an oxidative species in an effective amount to degrade a pesticide in said fertigation water; and collecting treated effluent.

129. The method of claim 128, wherein the at least one anode is a boron doped diamond (BDD) electrode that continuously produces reactive oxygen species selected from O.sub.2, O.sub.3, H.sub.2O.sub.2 and OH.

130. The method of claim 128, wherein chlorate species formed in said fertigation water is below acceptable levels of below about 2 mg/L.

131. The method of claim 128: (a) the current density is at least about 0.76 mA/cm.sup.2 to about 9.09 mA/cm.sup.2, about 1.14 mA/cm.sup.2, about 2.27 mA/cm.sup.2, about 3.41 mA/cm.sup.2, about 4.55 mA/cm.sup.2, about 6.82 mA/cm.sup.2 or about 9.09 mA/cm.sup.2; and/or (b) the pH of the nutrient aqueous solution during treatment is at least about 5.4 to about 8.5 or about 5.5 to about 6.5; and/or (c) the flow rate is selected to provide a treatment residence time of up to about 30 minutes, up to about 20 minutes or up to about 10 minutes; and/or (d) conducted at about room temperature and/or is conducted under ambient light.

132. The method of claim 128, wherein the pesticide is an organophosphate pesticide or a carbamate pesticide.

133. The method of claim 132, wherein the pesticide is glyphosate or paclobutrazol.

134. The method of claim 14, wherein the pesticide is a breakdown product aminomethylphosphonic acid (AMPA).

135. The method of claim 128, wherein the fertigation water is contaminated with one or more of Roundup™, Glyfos™, Bonzi™, Downsize™, Paczo™, Piccolo™ and Piccolo 10XC™.

136. An in situ oxidant producing method for the treatment of fertigation water, comprising: flowing fertigation water through an electrochemical cell comprising a boron doped diamond (BDD) anode and at least one complementary stainless steel cathode for a time effective to degrade placlobutrazol while simultaneously adjusting one or more of current density, flow rate and pH; and collecting effluent treated fertigation water.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0143] The above and other aspects, advantages, and features of this disclosure will become more apparent by describing in further detail exemplary embodiments thereof with reference to the accompanying drawings, in which:

[0144] FIG. 1 is a schematic showing proposed mechanisms of pathogen inactivation with an emphasis on the cycle of reactions constituting regenerative in situ electrochemical hypochlorination (mediated electrolysis).

[0145] FIG. 2: (A) Electrochemical Flow Cell (EFC) testbed schematic showing the principle components and the direction of the electrical current depicted by arrows used for the experimental setup and (B) the EFC with red arrows depicting the flow path and (C) monitoring and controlling components for flow rate (F), current (A), voltage (V), and the use of the power supply (P).

[0146] FIG. 3: Inactivation of Rhizoctonia solani (R. solani) as a function of contact time, while maintaining a constant current density of 0.76 mA/cm.sup.2. The test solution only contained deionized water with free floating mycelia and did not contain fertilizer or chloride salts for the experiment. Without the presence of a supporting electrolyte in solution gave an operating voltage for this specific experiment˜32 volts. Error bars are ±SEM, N=3, n=3.

[0147] FIG. 4: (A) Inactivation of Rhizoctonia solani as a function of current density and contact time with 20 mg/L of chloride in solution with no fertilizer present, and (B) effluent free chlorine concentration from the EFC after treatment of Rhizoctonia solani with 20 mg/L of chloride with no fertilizer present. Error bars are ±SEM, N=3, n=3.

[0148] FIG. 5: Effluent free chlorine measured from the EFC as a function of current density, contact time, as well as varying the concentration of fertilizer in solution. All of these experiments were conducted with a chloride concentration of 20 mg/L. Error bars are ±SEM, N=3, n=3. Where error bars are not shown they are too small to be visible behind the symbol.

[0149] FIG. 6: (A) Inactivation of Rhizoctonia solani as a function of current density with a fertilizer concentration of 0.5 g/L and increasing chloride concentration, and (B) effluent free chlorine concentrations observed under the same parameters while increasing the concentration of chloride. Error bars are ±SEM, N=3, n=3.

[0150] FIG. 7: (A) Rhizoctonia solani inactivation as a function of current density and contact time with 20 mg/L of chloride and 0.5 g/L of fertilizer in solution, and (B) effluent free chlorine from the EFC with applying variable current densities and contact times with the same test solution. Error bars are ±SEM, N=3, n=3.

[0151] FIG. 8: (A) Nitrogen dynamics as a function of current density (1.14 & 2.27 mA/cm.sup.2) and contact time of the solution containing (NH.sub.4).sub.2SO.sub.4 as the supporting electrolyte (relative to 0.05 g/L of 20-8-20 Plant Prod fertilizer) and 20 mg/L of chloride. 8(B) shows effluent free chlorine concentration as a function of current density and contact time. Error bars are ±SEM, N=3, n=3.

[0152] FIG. 9: TOC and TN of the organic fertilizer solution when treated with DSA's.

[0153] FIG. 10A-10B: Concentration of different ions from the organic fertilizer solution when treated with DSA's.

[0154] FIG. 11A-11C: TOC (total organic carbon) and TN (total nitrogen) of the organic fertilizer solution when treated with BDD electrodes.

[0155] FIG. 12A-12B: Concentration of different ions from the organic fertilizer solution when treated with DSA's.

[0156] FIG. 13A: Inactivation of R. solani in the absence of both fertilizer or chloride (only pathogen and deionized water present). The solution was passed through the EFC at variable contact times and applied the current densities of 1.14 and 2.27 mA/cm.sup.2. Error bars are ±SEM, n=3. B-D show levels of TN, nitrate, ammonium, sulphate and calcium with varying contact times.

[0157] FIG. 14: Inactivation of R. solani with the presence of fertilizer but without the presence of chloride in solution. The solution was passed through the EFC with applying various current densities and contact times to treat the fertigation solution. Error bars are ±SEM, n=3.

[0158] FIG. 15: Effluent-free chlorine concentrations produced by BDD electrodes with and without the presence of fertilizer in solution. The legend in the top right corner depicts the current densities applied to the solution over various contact times. Error bars are ±SEM, n=3.

[0159] FIG. 16: Perchlorate analysis by spectrophotometric methods with samples collected from the EFC with BDD electrodes. The solution only contained chloride and applied various current densities and contact times of the solution with the electrodes. Error bars are ±SEM, n=3.

[0160] FIG. 17: The solution contained 20 mg/L of chloride and 0.5 g/L of fertilizer and monitored for (A) the inactivation of R. solani and (B) the free chlorine produced as a function of contact time and current density. Error bars are ±SEM, n=3.

[0161] FIG. 18: Concentrations of nitrate, ammonium and sulphate when applying a current density of 9.09 mA/cm.sup.2 to the solution with varying contact times. The solution contained both fertilizer and chloride during treatment. Error bars are ±SEM, n=3.

[0162] FIGS. 19A-19C: A. Degradation of NPOC by applying two different current densities over variable contact times of the solution passing through the EFC. The solution only contained the pathogen and deionized water in solution and showing that NPOC is directly related to dissolved components originating from the pathogen. Error bars are ±SEM, n=3. B-C show total protein and ion concentrations with different contact times.

[0163] FIGS. 20A-20B: Experimental design in the greenhouse depicting (A) top view of the randomized complete block design with 4 growth tables and randomized troughs for each respective treatment type. The direction of flow (B) was from reservoir 1 to treatment and enters the second reservoir, following by the distribution to each ornamental crop. Each treatment had its own irrigation setup that would distribute the fertigation solution to all 4 growth tables.

[0164] FIG. 21: Photograph of plants during week 1 with inserted spikes which provided the irrigation solution to the soil. The irrigation water is drained through the soil and captured in troughs, which returned to each respective reservoir for further treatment.

[0165] FIG. 22: Measured parameters in plant health following 6 weeks of growth following different water treatment types. Plants were measured for the number of leaves, leaf area, average petiole length and weight of plants. Error bars are ±SEM, n=3.

[0166] FIG. 23: Photo providing the visual differences between treatments following 6 weeks of growth in the greenhouse. The positive control was shown to have critical damage to the ornamental crop, while all other treatments were determined to be healthy. No differences could be found for all water treatment technologies in comparison to the negative control.

[0167] FIG. 24: Nutrient dynamics of nitrate following each treatment over the number of recirculations. Yellow line depicts the time when the recirculated solution was supplied with an additional solution (0.5 g/L of 20-8-20 water soluble fertilizer). Error bars are ±SEM, n=3.

[0168] FIG. 25: Nutrient dynamics of phosphate, ammonium and potassium following each treatment over the number of recirculations. Yellow line depicts the time when the recirculated solution was supplied with an additional solution (0.5 g/L of 20-8-20 water soluble fertilizer). Error bars are ±SEM, n=3.

[0169] FIG. 26: Nutrient dynamics of sulphate, magnesium and calcium following each treatment over the number of recirculations. Yellow line depicts the time when the recirculated solution was supplied with an additional solution (0.5 g/L of 20-8-20 water soluble fertilizer). Error bars are ±SEM, n=3.

[0170] FIG. 27: Nutrient dynamics of iron following each treatment over the number of recirculations. Yellow line depicts the time when the recirculated solution was supplied with an additional solution (0.5 g/L of 20-8-20 water soluble fertilizer). Error bars are ±SEM, n=3.

[0171] FIG. 28A-28B: Schematic of (28A) randomized complete block design showing the location of all treatments and holes where tubing, as well as plants are located. A photo (28B) shows the randomized complete block design from the perspective of the experimenter.

[0172] FIG. 29: Pathogen inactivation rates through different experiments in the effluent (blue) and bulk (red) of the fertigation solution, while using various current densities. Error bars are ±SEM, n=3.

[0173] FIG. 30: Concentration of free chlorine (blue) and combined chlorine (red) across different experiments with varying current densities applied to solution over time. Error bars are ±SEM, n=3.

[0174] FIGS. 31A-31C: Photograph of plants following 14 days of growth after transplant and being treated with the EFC system under (A) fertilizer containing NH.sub.4.sup.+, (B) fertilizer with ammonium but with added UV light and (C) fertilizer which only contains NO.sub.3.sup.− and is treated with the EFC system.

[0175] FIGS. 32A-32E: Plant performance following treatment of the solution under 3 different experiments, while using 3 current densities. Measured plant parameters were (A) number of leaves, (B) leaf area, (C) leaf fresh weight, (D) biomass (leaf and root dry weights) and (E) shoot/root ratio. Error bars are ±SEM, n=3.

[0176] FIG. 33: Solution turbidity following treatment from AOP, BDD, DSA and ozone with treatment time. Error bars are ±SEM, n=3.

[0177] FIGS. 34A-34B: Concentration of (A) NPOC and (B) TN in solution following treatment by AOP, BDD, DSA and ozone at various treatment time intervals. Error bars are ±SEM, n=3.

[0178] FIG. 35: Phosphate concentration in solution following treatment by AOP, BDD, DSA and ozone at various treatment time intervals. Error bars are ±SEM, n=3.

[0179] FIGS. 36A-36B: Measured concentrations of (A) ammonium and (B) nitrate in solution following treatment by AOP, BDD, DSA and ozone at various treatment time intervals. Error bars are ±SEM, n=3.

[0180] FIG. 37: Calcium concentrations in solution following treatment by AOP, BDD, DSA and ozone at various treatment time intervals. Error bars are ±SEM, n=3.

[0181] FIGS. 38A, 38B and 38C: Growth chamber used to grow Lemna minor plants showing (A) outside of the chamber covered by black tarp, LED light and laptop for data logging over top of the chamber (B) Inside of the chamber with Red:Blue:White ratio used to grow plants, and (C) Erlenmeyer flasks containing Lemna plants under white light for demonstration with temperature and humidity sensors on the right hand side;

[0182] FIG. 39: Heat map of PAR levels for each ‘grid’ inside the growth chamber with red boxes depicting areas of low intensity, while higher light intensities were found in the middle of the chamber depicted by green boxes;

[0183] FIGS. 40A to 40D: (A) shows a batch reactor system built in the Controlled Environment Systems Research facility for injecting ozone through the bottom of the batch reactor (Left) and the solution is then passed through the UV chamber by gravity to provide the AOP treatment (Right); (B) shows an Electrochemical Flow Cell (EFC) testbed schematic showing the principle components and the direction of the electrical current depicted by arrows used for the experimental setup and (C) the EFC with red arrows depicting the flow path and (D) monitoring and controlling components for flow rate (F), current (A), voltage (V), and the use of the power supply (P).

[0184] FIGS. 41A and 41B: The effects of glyphosate (Glyfos™) on (A) final number of Lemna minor plants, fronds and (B) dry weights with increasing concentration on the horizontal axis. Plant samples were measured after a growth period of 7 days in the growth chamber. Error bars are ±SEM, n=3;

[0185] FIGS. 42A and 42B: Demonstration the growth of Lemna minor (A) without the presence of glyphosate and (B) with of 15 mg/L of glyphosate in solution and grown over a period of 7 days in the growth chamber,

[0186] FIGS. 43A and 43B: The effects of paclobutrazol (Bonzi™) on (A) the final number of Lemna minor plants, fronds, and (B) their dry weights with increasing concentration on the horizontal axis. Plant samples were measured after a growth period of 7 days in the growth chamber. Error bars are ±SEM, n=3;

[0187] FIGS. 44A and 44B: Demonstration the growth of Lemna minor (A) without the presence of paclobutrazol and (B) with of 5 mg/L of paclobutrazol in solution and grown over a period of 7 days in the growth chamber,

[0188] FIG. 45: The NPOC and TN measured following treatment from DSA and BDD electrodes on glyphosate and paclobutrazol standards in a batch cell. The solution also contained 20 mg/L of chloride with both systems for treating the water. Error bars are ±SEM, n=3;

[0189] FIGS. 46A and 46B: Treatment of solution using the BDD and DSA electrodes for treating the solution from chemical standards (A) glyphosate, AMPA and (B) paclobutrazol using a current density of 2.27 mA/cm.sup.2 with a 6-minute contact time. The treatment was performed in a batch cell with constant mixing. Only 20 mg/L of chloride and the chemical standard were present in solution. Error bars are ±SEM, n=3;

[0190] FIGS. 47A and 47B: Measured parameters for plant health in relation to the current density with (A) the number of plants, fronds and (B) the total dry weight of plants. The system was configured to the EFC with only the presence of 20 mg/L Cl.sup.− in solution. Error bars are ±SEM, n=3;

[0191] FIG. 48: Measured values of free chlorine in the effluent stream from the EFC in relation to the current density applied to the solution. The system was configured to the EFC with only the presence of 20 mg/L Cl.sup.− in solution. Error bars are ±SEM, n=3;

[0192] FIGS. 49A and 49B: Results on plant growth and reproduction after treatment with AOP, BDD, DSA and O.sub.3 on the commercial product Roundup. Parameters measured were (A) the number of plants, fronds and (B) the dry weights of plants in relation to the contact time each treatment. The electrochemical systems were configured to the EFC with only the presence of 20 mg/L Cl.sup.− in solution. Error bars are ±SEM, n=3;

[0193] FIGS. 50A and 50B: Results on plant growth and reproduction after treatment with AOP, BDD, DSA and O.sub.3 on the commercial product Bonzi™. Parameters measured were (A) the number of plants, fronds and (B) the dry weights of plants in relation to the contact time each treatment. The electrochemical systems were configured to the EFC with only the presence of 20 mg/L Cl.sup.− in solution. Error bars are ±SEM, n=3; and

[0194] FIGS. 51A and 51B: Results on plant growth and reproduction after treatment with AOP, BDD, DSA and 03 on the commercial product Bonzi™. Parameters measured were (A) the number of plants, fronds and (B) the dry weights of plants in relation to the contact time each treatment. The electrochemical system was configured to the EFC with only the presence of 20 mg/L Cl.sup.− in solution and recirculated 3 times with a 6-minute contact time. Error bars are ±SEM, n=3.

DETAILED DESCRIPTION

[0195] Reference will now be made in detail to exemplary embodiments, examples of which are illustrated in the accompanying drawings, wherein like reference numerals refer to like elements throughout. In this regard, the present exemplary embodiments may have different forms and should not be construed as being limited to the descriptions set forth herein. Accordingly, the exemplary embodiments are merely described below, by referring to the figures, to explain aspects of the present description.

[0196] As used herein, the terms “invention” or “present invention” are non-limiting terms and not intended to refer to any single aspect of the particular invention but encompass all possible aspects as described in the specification and the claims.

[0197] All publications, patent applications, patents, and other references mentioned herein are incorporated by reference in their entirety. The publications and applications discussed herein are provided solely for their disclosure prior to the filing date of the present application. Nothing herein is to be construed as an admission that the present invention is not entitled to antedate such publication by virtue of prior invention. In addition, the materials, methods, and examples are illustrative only and are not intended to be limiting.

[0198] In the case of conflict, the present specification, including definitions, will control.

[0199] Unless defined otherwise, all technical and scientific terms used herein have the same meaning as is commonly understood by one of skill in the art to which the subject matter herein belongs. It will be further understood that terms, such as those defined in commonly used dictionaries, should be interpreted as having a meaning that is consistent with their meaning in the context of the relevant art and the present disclosure, and will not be interpreted in an idealized or overly formal sense unless expressly so defined herein.

[0200] As used herein, the following definitions are supplied in order to facilitate the understanding of the present invention.

[0201] As used herein, the articles “a” and “an” preceding an element or component are intended to be non-restrictive regarding the number of instances (i.e. occurrences) of the element or component. Therefore, “a” or “an” should be read to include one or at least one, and the singular word form of the element or component also includes the plural unless the number is obviously meant to be singular.

[0202] It will be further understood that the terms “comprises” and/or “comprising,” or “includes”, “including” and/or “having” and their inflections and conjugates denote when used in this specification, specify the presence of stated features, regions, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, regions, integers, steps, operations, elements, components, and/or groups thereof.

[0203] It will be understood that any component defined herein as being included may be explicitly excluded from the claimed invention by way of proviso or negative limitation.

[0204] As used herein, the term “about” refers to variation in the numerical quantity. In one aspect, the term “about” means within 10% of the reported numerical value. In another aspect, the term “about” means within 5% of the reported numerical value. Yet, in another aspect, the term “about” means within 10, 9, 8, 7, 6, 5, 4, 3, 2, or 1% of the reported numerical value.

[0205] Should a range of values be recited, it is merely for convenience or brevity and includes all the possible sub-ranges as well as individual numerical values within and about the boundary of that range. Any numeric value, unless otherwise specified, includes also practical close values and integral values do not exclude fractional values. Sub-range values and practically close values should be considered as specifically disclosed values.

[0206] As used herein the term ‘may’ denotes an option or an effect which is either or not included and/or used and/or implemented and/or occurs, yet the option constitutes at least a part of some embodiments of the invention or consequence thereof, without limiting the scope of the invention.

[0207] The phrase “and/or,” as used herein in the specification and in the claims, should be understood to mean “either or both” of the elements so conjoined, e.g., elements that are conjunctively present in some cases and disjunctively present in other cases. Other elements may optionally be present other than the elements specifically identified by the “and/or” clause, whether related or unrelated to those elements specifically identified unless clearly indicated to the contrary.

[0208] As used herein, expressions such as “at least one of,” when preceding a list of elements, modify the entire list of elements and do not modify the individual elements of the list.

[0209] “About,” “approximately,” or “substantially” as used herein is inclusive of the stated value and means within an acceptable range of deviation for the particular value as determined by one of ordinary skill in the art, considering the measurement in question and the error associated with measurement of the particular quantity (i.e., the limitations of the measurement system). For example, “about,” “approximately,” or “substantially” can mean within one or more standard deviations, or within +30%, 20%, 10%, 5% of the stated value.

[0210] “Controlled-environment agriculture” (CEA), as used herein, includes technologies where all environmental factors can be controlled. Factors may include artificial control of light, environmental control (e.g. humidity, temperature, gases) and fertigation. CEA may include for example greenhouse, hydroponics, aquaculture, and aquaponics. CEA may also incorporate aspects of urban agriculture for plant growth such as raised beds, vertical gardening, container gardening and “growth chamber” production.

[0211] “Fertigation”, as used herein, is combining fertilizer and irrigation, a common industry term used to denote the delivery of fertilizer via the irrigation solution (i.e.) irrigation water. Such water is referred to as fertigation water or fertigation solution (the terms are used synonymously herein). Fertigation water is essentially nutrient feed water as it contains the essential elements required for healthy plant growth. It consists of various proportions of fertilizers dissolved in water or a blend of fertilizer solutions to provide the nutrient complement required for healthy plant growth.

[0212] Captured fertigation water is leached nutrient feed water, that is, the fertigation water that has been captured after passing though the growing substrate. It may or may not be recycled. It can also be referred to as leachate or leach.

[0213] “Fertilizer water/solution” as used herein is a stock solution consisting of a single fertilizer, or several compatible fertilizers, dissolved in water (aqueous solution) containing the essential nutrients for plant growth. Fertilizers may be inorganic (chemical, wholly or partially synthetic origin and exclude carbon-containing materials) or organic (derived from the remains or byproducts of natural organisms such as animal excreta (manure), human excreta, and vegetable matter (e.g. compost and crop residues). Naturally occurring organic fertilizers include animal wastes from meat processing, peat, manure, slurry, and guano. Inorganic fertilizers may be classified according to whether they provide a single nutrient (e.g., K, P, or N), in which case they are classified as “straight fertilizers.” “Multinutrient fertilizers” (or “complex fertilizers”) provide two or more nutrients, for example N and P. Nitrogen-based straight fertilizers include ammonia and its solutions, ammonium nitrate (NH.sub.4NO.sub.3) and urea. The main straight phosphate fertilizers are the superphosphates. The main potassium-based straight fertilizer is Muriate of Potash (MOP).

[0214] “Hydroponic” as used herein is a method of growing plants without soil but instead use a mineral nutrient solution in a water solvent. Other non-soil substrates can be used to help with physical support of plant/roots during growth.

[0215] “Organic hydroponics” as used herein is a hydroponic culture system utilizing organic fertilizer. “Bioponics” as used herein is the soilless system components such as the media beds, troughs, structural supports such as rafts and so forth.

[0216] “Biomass” as used herein is a total mass of a plant (living matter) in a given area or volume. Biomass may also refer to a renewable resource of waste such as crop waste, wood, manure, types of garbage and the like.

[0217] Crop, as used herein, is a cultivated plant grown on a large scale commercially. The crop is understood not to be limited as understood by one of skill in the art. A crop may be edible or ornamental. “Plant” may be used interchangeably for “crop” herein. Within the scope of present invention, crops/plants to be protected typically comprise perennial and annual crops, such as but not limited in any manner to berry plants for example blackberries, blueberries, cranberries, raspberries and strawberries; cereals for example barley, maize (corn), millet, oats, rice, rye, sorghum triticale and wheat; fibre plants for example cotton, flax, hemp, jute and sisal; field crops for example sugar and fodder beet, coffee, hops, mustard, oilseed rape (canola), poppy, sugar cane, sunflower, tea and tobacco; fruit trees for example apple, apricot, avocado, banana, cherry, citrus, nectarine, peach, pear and plum; grasses for example Bermuda grass, bluegrass, bentgrass, centipede grass, fescue, ryegrass, St. Augustine grass and Zoysia grass; herbs such as basil, borage, chives, coriander, lavender, lovage, mint, oregano, parsley, rosemary, sage and thyme; legumes for example beans, lentils, peas and soya beans; nuts for example almond, cashew, ground nut, hazelnut, peanut, pecan, pistachio and walnut; palms for example oil palm; ornamentals for example flowers (floriculture), shrubs and trees; other trees, for example cacao, coconut, olive and rubber; vegetables for example asparagus, aubergine, broccoli, cabbage, carrot, cucumber, garlic, lettuce, marrow, melon, okra, onion, pepper, potato, pumpkin, rhubarb, spinach and tomato; vines for example grapes; and Cannabis for example, Cannabis sativa, Cannabis indica and Cannabis ruderalis.

[0218] The useful plants and/or target crops in accordance with the invention include conventional as well as genetically enhanced or engineered varieties.

[0219] Crop security, as used herein, is being free from danger or threat from pathogens, phytotoxic chemical contaminants, and/or nutrient imbalances.

[0220] The term “remove” as used herein is used meant to substantially eliminate to an undetectable level or a level safe for a living organism and/or crop.

[0221] The term “degrade” as used herein means to transform into a benign substance that is environmentally compatible.

[0222] The term “agrichemical” as used herein is a chemical used in agriculture, such as a pesticide or a fertilizer.

[0223] As used herein the term “pesticide” is a composite term that includes all chemicals that are used to kill or control pests. Pesticides are used to protect crops against insects, weeds, fungi, and other pests and play a significant role in food production by protecting or increasing yields, and the number of times per year a crop can be grown on the same land. In agriculture pesticides include herbicides (weeds), insecticides (insects), fungicides (fungi), nematocides (nematodes), and rodenticides (vertebrate poisons).

[0224] Pesticides include organophosphate pesticides and carbamate pesticides such as glyphosate (IUPAC name: N-(phosphonomethyl)glycine) and AMPA (aminomethylphosphonic acid, a toxic break down product of glyphosate) and paclobutrazol.

[0225] The acronym EFC, as used herein, is an electrochemical flow cell.

[0226] Disinfect, disinfecting, inactivate, are each used synonymously herein, as meaning to destroy and/or inhibit growth of a pathogen, to render a pathogen inert and not harmful to crops/plants. A “susceptible” pathogen is likely or liable to be influenced or harmed by the regenerated disinfectant as described herein.

[0227] The term “effective amount” means the quantity of disinfectant that is capable of producing an effect on the growth of pathogen. Controlling or modifying effects include all deviation from natural development, such as killing, retardation and the like, and prevention includes barrier or other defensive formation in or on a plant to prevent infection.

[0228] The acronym DSA, as used herein, is a dimensionally stable anode. Dimensionally stable anodes are basically a titanium skeleton covered with electrocatalytically active mixtures of oxides. These anodes consist of mainly ruthenium oxide deposited on titanium along with other metallic oxides like platinum, iridium, palladium, rodium and titanium. Dimensionally stable anodes preserve their shape and voltage characteristics even under severe conditions of anodic attack. They exhibit dimensional stability, longer life and function effectively at higher current densities.

[0229] Regenerative mediated electrolysis, as used herein, is a process in which chloride ions are transformed to free chlorine forms (e.g., hypochlorous acid) which neutralizes pathogens and in this process releases chloride ions back to the solution. The chloride ions migrate back to the anode through electrostatic migration where once again they can be transformed to free chlorine forms leading to further pathogen inactivation.

[0230] A general non-limiting overview of the invention and practising the invention is presented below. The overview outlines exemplary practice of embodiments/aspects of the invention, providing a constructive basis for variant and/or alternative and/or divergent aspects/embodiments, some of which are subsequently described.

[0231] In situ electrochemical methods and systems are herein developed for the treatment of aqueous solutions for use in a variety of agricultural, municipal and industrial applications. In CEA operations treatment of recycling fertigation water is desired in order to decrease pathogens, provide stabile nutrients to the growing plants, degrade contaminants such as pesticides; degrade recalcitrant organic contaminants; and/or degrade organic fertilizers to provide nutrient ions for plant growth. Solutions of organic waste can be treated to degrade and solubilize plant nutrients, and thus be transformed into a source of organic fertigation water for use in CEA such as in hydroponics. Municipal and industrial used water (waste water) can be subjected to the in situ electrochemical methods of the invention to degrade organic and non-organic contaminants and destroy pathogens. The in situ electrochemical treatment systems of the invention can also be incorporated within a wastewater treatment plant.

[0232] In one non-limiting embodiment, in situ electrochemical methods, and systems incorporating the methods, are herein developed for the treatment of fertigation water that is used primarily in CEA operations where recycling of fertigation water is desired.

[0233] This demonstrates many benefits and substantiates the process which can be implemented in Controlled Environment Agriculture. The electrochemical process for in situ treatment of a recirculating nutrient can be used successfully for commercial floriculture production with plants propagated in soil. The technology is effective for pathogen removal without posing phytotoxic effects to crops. The technology is also demonstrated that it can be utilized in conventional hydroponic systems. With fertilizers containing NH.sub.4.sup.+, the system can be used successfully with lower current densities, which do not release chloramines at concentrations higher than the phytotoxic threshold (0.2 mg/L NH.sub.4Cl). If higher current densities are needed for operations, tertiary treatment methods such as UV light may be used to produce crops without negative impacts on growth. Furthermore, NO.sub.3 based fertilizers without the presence of NH.sub.4.sup.+ presents the best option for growers and provides crop yields in which are equivalent or enhanced in comparison to conventional hydroponic methods without water treatment.

[0234] The electrochemical process with BDD electrodes can be successfully used for mineralizing organic materials and solubilize nutrients in which can be used for hydroponics or conventional irrigation systems. This allows for a variety of organic waste materials to be used in hydroponic and other irrigation systems decreasing reliance on synthetic fertilizers. The electrochemical processes are also effective to remove/degrade undesired agrichemicals such as pesticides from the fertigation water.

[0235] An electrochemical flow cell (EFC) system is employed with each cell comprising a plurality of dimensionally stable anodes (DSA) and complementary cathodes (collectively an electrode array) supported within a casing/housing that may be any suitable material such as but not limited to acrylic. In one embodiment, the DSA may be RuO.sub.2 and the complementary cathode stainless steel. The EFC may comprise a set of six RuO.sub.2 DSA and a set of five complementary stainless steel cathodes spaced apart therefrom. In one embodiment, each cathode is spaced about 2 mm apart from each of its complementary anode. Generally, the closer the electrodes, the better the electron transfer is, and the less conductivity the influent fertigation water needs to have. However, the electrodes may be further apart and still be effective. The electrodes should not be in direct contact with each other.

[0236] Fertigation water to be treated is pumped via a variable speed peristaltic pump into the bottom entry port of the EFC housing and upwards through the electrodes, exiting the cell at an outflow port at the top of the housing. A power supply is connected to both anode and cathode of the flow cell. Multimeters are provided with direct connection to the anode and cathode of the cell for measuring the applied voltage. It is understood by one of skill in the art, that the electrochemical flow cell (EFC) system employed may be scaled to a desired size and volume of fertigation water, used in series, and further connected to an irrigation system to deliver the treated fertigation water to the crop and collect run off for pooling and recirculation. It is also understood that the scaled system may further comprise a variety of sensors and so forth for operation. A pre-filter may be added in the influent fertigation water stream or a post-filter may be added in the effluent treated fertigation stream to catch particles. The EFC may have any practically useful shape that may be utilized for fertigation water purification purposes. The shape of the EFC cell is not limited.

[0237] The EFC according to any embodiment, may further include an oxidation-reduction potential sensor, a pH sensor, a chlorine sensor, a conductivity sensor, a flow rate sensor, a temperature sensor, or a combination thereof.

[0238] In another embodiment, EFC may include two or more sequentially connected individual flow-through cells. The treated fertigation water may be delivered to the next flow-through cell, where a purification process is repeated.

[0239] In an embodiment, the electrodes used are BDD. In this aspect, advantageously the fertigation water is nutrient enhanced during treatment thereof by releasing ammonium into solution that is converted to nitrates thus being bioavailable to the crop(s) irrigated with the treated fertigation solution. Thus the recycling of fertigation water within the system in accordance with the methods described herein functions to enrich the treated fertigation water (with ammonium, nitrate, sulphate and calcium) and encourage crop growth. In this embodiment using BDD as the anodes, chloride may further be added to enhance inactivation of pathogens as is understood by one of skill in the art.

[0240] Electrochemical methods, and systems incorporating the methods, are now developed for the treatment of fertigation water that is used primarily in CEA operations where recycling of fertigation water is desired. The methods are effective to remove/degrade undesired agrichemicals such as pesticides from the fertigation water. It is desired to remove harmful pesticides such as for example glyphosate and paclobutrazol from the fertigation water in order not to be harmful to the crop to which the fertigation water is used. Further, pesticides can be absorbed by plants through the leaves and roots and can translocate to other parts of the plant. Crops irrigated with pesticide contaminated fertigation water are undesirable for human health.

[0241] In an embodiment, electrochemical treatment of fertigation water, as used in controlled environment agriculture, is used to remove/degrade pesticides to safe/safer levels for both the irrigated crop as well as for humans when the crop is consumed. The method and system are useful in recirculating irrigation systems employing fertigation water.

[0242] It is surprisingly demonstrated that electrochemical treatment of irrigation water, fertigation water, using either or both DSA and BDD effectively removes/degrades glyphosate and paclobutrazol therein. The DSA electrodes were demonstrated to degrade glyphosate more effectively than paclobutrazol. BDD electrodes were demonstrated to degrade paclobutrazol more effectively than glyphosate. Both DSA and BDD can however, be used effectively to degrade both glyphosate and paclobutrazol. Both of these electrochemical systems may incorporate chlorination monitored with respect to plant growth. The water treatment methods (DSA and BDD) were demonstrated effective at removing glyphosate from solution to levels that would remediate plant health. BDD electrodes had shown to also increase plant growth following treatment with glyphosate in comparison to the control sample. All of the water treatment methods were also shown to remove paclobutrazol in solution but at lower efficiency to that of glyphosate. Using BDD electrodes with longer contact times increased the efficiency of paclobutrazol removal thus improving water quality and plant growth.

[0243] The electrochemical methods used herein demonstrated the ability to remove pesticides such that they could be used in crop production systems using fertigation water.

[0244] An electrochemical flow cell (EFC) system is employed with each cell comprising a plurality of dimensionally stable anodes (DSA) and complementary cathodes (collectively an electrode array) supported within a casing/housing that may be any suitable material such as but not limited to acrylic. In one embodiment, the DSA may be RuO.sub.2 and the complementary cathode stainless steel. The EFC may comprise a set of six RuO.sub.2 DSA and a set of five complementary stainless steel cathodes spaced apart therefrom. In one embodiment, each cathode is spaced about 2 mm apart from each of its complementary anode. Generally, the closer the electrodes, the better the electron transfer is, and the less conductivity the influent fertigation water needs to have. However, the electrodes may be further apart and still be effective. The electrodes should not be in direct contact with each other.

[0245] Fertigation water to be treated is pumped via a variable speed peristaltic pump into the bottom entry port of the EFC housing and upwards through the electrodes, exiting the cell at an outflow port at the top of the housing. A power supply is connected to both anode and cathode of the flow cell. Multimeters are provided with direct connection to the anode and cathode of the cell for measuring the applied voltage. It is understood by one of skill in the art, that the electrochemical flow cell (EFC) system employed may be scaled to a desired size and volume of fertigation water, used in series, and further connected to an irrigation system to deliver the treated fertigation water to the crop and collect run off for pooling and recirculation. It is also understood that the scaled system may further comprise a variety of sensors and so forth for operation. A pre-filter may be added in the influent fertigation water stream or a post-filter may be added in the effluent treated fertigation stream to catch particles. The EFC may have any practically useful shape that may be utilized for fertigation water purification purposes. The shape of the EFC cell is not limited.

[0246] The EFC according to any embodiment, may further include an oxidation-reduction potential sensor, a pH sensor, a chlorine sensor, a conductivity sensor, a flow rate sensor, a temperature sensor, or a combination thereof.

[0247] In another embodiment, EFC may include two or more sequentially connected individual flow-through cells. The treated fertigation water may be delivered to the next flow-through cell, where the purification process is repeated.

[0248] Using this electrochemical cell system, the removal/degradation of a pesticide (for example, glyphosate and/or paclobutrazol) is achieved through the manipulation, in isolation or in combination, of the applied current, contact time.

[0249] In a further embodiment, the electrodes used are BDD to continuously produce reactive oxygen species (ROS) to remove/degrade a pesticide (for example, glyphosate and/or paclobutrazol). In this aspect, advantageously the fertigation water is nutrient enhanced during treatment thereof by releasing ammonium into solution that is converted to nitrates thus being bioavailable to the crop(s) irrigated with the treated fertigation solution. Thus the recycling of fertigation water within the system in accordance with the methods described herein functions to enrich the treated fertigation water (with ammonium, nitrate, sulphate and calcium) and encourage crop growth.

[0250] The methods and systems described herein are suitable for use for any fertigation water that comprises either inorganic or organic fertilizer and even mixtures thereof. In aspects, organic fertilizer water is employed with an EFC incorporating BDD.

[0251] The methods and systems may be employed in any fertigation irrigation system for any type of CEA employing recycling of their fertigation water.

[0252] The methods and systems described herein are suitable for the treatment of any fertigation water used for any desired crop, edible or ornamental. In aspects, the methods and systems are beneficial for growing cannabis such as for example in greenhouses and further hydroponically utilizing treated fertigation water of the invention and recycled treated fertigation water.

[0253] The methods and systems described herein are suitable for use for any fertigation water that comprises either inorganic or organic fertilizer and even mixtures thereof. In aspects, organic fertilizer water is employed with an EFC incorporating BDD.

[0254] The methods and systems may be employed in any fertigation irrigation system for any type of CEA employing recycling of their fertigation water.

[0255] The methods and systems described herein are suitable for use for any desired crop, edible or ornamental. In aspects, the methods and systems are beneficial for growing cannabis such as for example in greenhouses and further hydroponically utilizing treated fertigation water of the invention and recycled treated fertigation water.

[0256] To summarize, in situ electrochemical systems and methods are now developed for the treatment of aqueous solutions for a variety of applications. Aqueous solutions, such as fertigation water, can be continuously treated in agricultural irrigation systems to degrade undesired contaminants and destroy pathogens—both of which are harmful to crops/plants. It has also been surprisingly found that the systems and methods maintain sustainable nutrient solutions for the growing plants without toxic built up of chloramine or chloride. As such, the systems and methods can be continuously used in agriculture for a crop for weeks and months as desired. The systems and methods are not only for treatment of the fertigation water (inorganic and organic fertigation water) but also used in a preventative manner in order that pathogens do not invade the fertigation water or if any amounts of contaminant such as an pesticide finds its way into the fertigation water, it will be degraded. The systems and methods of the invention can also be used to treat organic waste solutions and in this manner, make them suitable for use as an organic fertigation water.

[0257] The systems and methods of the invention also have use in industrial process water treatment. The systems and EFC cells can be incorporated into conventional water treatment systems for prevention of contamination by pathogens and recalcitrant organic contaminants and further, treatment of a water source can make it more potable for drinking and other uses. UV can be further used on treated effluent water.

[0258] The descriptions of the various embodiments and/or examples of the present invention have been presented for purposes of illustration but are not intended to be exhaustive or limited to the embodiments and/or examples disclosed. Many modifications and variations will be apparent to those of ordinary skill in the art without departing from the scope and spirit of the described embodiments. The terminology used herein was chosen to best explain the principles of the embodiments, the practical application, or to enable further understanding of the embodiments disclosed herein.

EXAMPLES

Example 1 Inactivation of Rhizoctonia solani in Fertigation Water Using Regenerative In Situ Electrochemical Hypochlorination with Ruthenium Oxide DSA

Materials and Methods

Pathogen Cultures

[0259] A pure culture of Rhizoctonia solani was provided courtesy of Dr. Allen Xue from the Plant Pathology Ottawa Research and Development Centre, Agriculture and Agri-Food Canada. Mycelia were inoculated onto potato dextrose agar (PDA) (B213400, Fisher Scientific, Canada) containing 0.1 g/L of streptomycin sulfate (BP910-50, Fisher Scientific, Canada) and 0.05 g/L of ampicillin sodium salt (BP1760-25, Fisher Scientific, Canada). The plates were then incubated on the laboratory bench inside a clear plastic container at room temperature (˜23° C.) and ambient light levels. After incubation for seven days the plates were fully covered with mycelia, at which point five 1 cm.sup.2 sections of the mycelia mat were excised from the outer edge of the petri dish and placed into 250 mL Erlenmeyer flasks, each containing 100 ml Potato Dextrose Broth (PDB) (B254920, Fisher Scientific, Canada). The suspension was then placed in an incubator (Innova 4340, New Brunswick Scientific, USA) for 8 days at 30° C. under a 12 hr photoperiod. The cultured mycelia were then transferred to a blender (HH-362, E.F. Appliances Canada LTD.) and blended for 30 seconds. A pipette (4642110, Thermo Scientific, USA) was used to inoculate 10 ml of the suspension into new Erlenmeyer flasks with 250 mL of PDB and further incubated for another 8 days under the same conditions previously described.

Test Solution Preparation

[0260] Rhizoctonia solani cultures were vacuum filtered through a 1.5 μm filter disk (Whatman 934-AH) to separate the mycelia from the liquid broth. The mycelia were rinsed off the filter disk with deionized (DI) water and deposited in a 500 mL sterile beaker and filled to 300 mL with DI water. The suspension was then transferred to a blender and blended for 1 minute. The blended suspension was then added to a 60-litre reservoir containing 30 litres of DI water. This solution was then subjected to the electrochemical treatment.

[0261] The fertilizer solutions with added chloride, in the form of potassium chloride ((P330-500), Fisher Scientific, Canada), were prepared by weighing out (TE 124S, Sartorius, Germany) appropriate amounts of stock material (20-8-20 Plant Prod, 10561, Master Plant-Prod Inc., Canada; ammonium sulphate (A702-3) and potassium chloride) to bring the final solution volume to the targeted concentrations for each experiment (Table 1). The Plant Prod fertilizer consisted of Nitrate (4.3 mmol/L), Phosphate (0.55 mmol/L), Ammonium (2.64 mmol/L) and Potassium (2.80 mmol/L) at 0.5 grams per liter of solution. Other ions in trace amounts are Sulphate (40 μmol/L), Sodium (150 μmol/L), Magnesium (60 μmol/L), Calcium (30 μmol/L) and Nitrite was not initially present. Individual macronutrient ions from a 0.5 g/L solution were measured with a Shimadzu HPLC system consisting of a DGU-20A3 degasser, a SIL-10AP autosampler, two LC-20AT pumps, two CDD-10A VP conductivity detectors, CTO-20AC column oven, and CBM-20A system controller. Total Nitrogen was measured using a Shimadzu TNM-1 unit (Shimadzu Scientific Instruments, USA).

TABLE-US-00001 TABLE 1 Fertigation solution composition summary for each experiment presented. Solution compositions are cross referenced with their respective figures for clarity. Chloride (Cl.sup.−) Fertilizer concentration concentration Figure (mg/L) Fertilizer type (g/L) FIG. 3  0 N/A 0 FIG. 4a & 4b 20 N/A 0 FIGS. 5 20 Plant Prod (20-8-20) 0-0.5 FIGS. 6a & 6b 20-50 Plant Prod (20-8-20) 0.5 FIGS. 7a & 7b 20 Plant Prod (20-8-20) 0.5 FIG. 8a & 8b 20 (NH.sub.4).sub.2SO.sub.4 0.02

Electrochemical Flow Cell and Operation Procedures

[0262] The electrochemical flow cell (EFC) system used consisted of a set of six RuO.sub.2 dimensionally stable anodes (DSA) (De Nora Tech, Concord, USA) and a complementary set of five stainless steel cathodes, spaced 2 mm apart, in an acrylic casing. The total area of the anodes was 1320 cm.sup.2. Solutions entered the cell from the bottom, passed upwards through the electrodes, and exited the cell at an outflow port at the top of the housing (FIGS. 2A & 2B). A power supply (DF1730SC 20A DC power supply, Gold Source, China) was connected to the anode and cathode of the flow cell. The applied current value was derived from the voltage drop measured across a precision current resistor (RS-50-100, RIEDON, Alhambra, Calif.) using a multimeter (Fluke 189, Fluke Corporation, Canada). A second multimeter (Fluke 87, Fluke Corporation, Canada) connected directly to the anode and cathode of the cell measured the applied voltage (FIG. 2C). A second multimeter is connected directly to the terminals of the anode and cathode array to measure the applied voltage. A variable speed peristaltic pump (Cole-Parmer 1-100 RPM) drew water from the test solution reservoir to the entry port located at the base of the flow cell.

[0263] The total free volume of the EFC, the internal volume of the housing less the volume of the electrode assembly, was 380 mL. The targeted contact times were achieved by adjusting the flow rates through the cell such that a given volume of solution would remain in contact with the electrodes for the desired time interval.

[0264] Untreated samples were collected from the main reservoir at the start, middle, and end of each experiment. Colony counts from each time point were averaged and used as the control or starting value for each test condition examined in a given experiment. Three effluent samples were collected from the outlet of the EFC for each treatment combination. The first sample was collected after three cell volumes (1140 ml) had passed through the flow cell, while samples two and three were collected after one and two additional flow cell volumes had passed through the system. Samples were collected in 40 ml clear plastic HDPE vials (20120121, Richard's Plastics, Canada). The pH (542, Corning, USA) and free chlorine concentration, for solutions containing chloride, were measured prior to microbial enumeration. Free chlorine from the bulk solution was measured according to the manufacturer's methods using DPD Test 'N Tube cuvette with free chlorine reagent set (2105545, Hach Company, USA) and a DR/850 portable colorimeter (4845000, Hach Company, USA). The samples were then serially diluted (10.sup.1, 10.sup.2, 10.sup.3 and 10.sup.4) in glass test tubes and a 100 μL aliquot from each was spread onto plates with PDA and antibiotics under a laminar flow hood. Plates were inverted and incubated at 30° C. under 12-hr photoperiod at 100 μmol.Math.m.sup.−2.Math.s.sup.−1 photosynthetically active radiation light for 2 days. Total colony forming units per milliliter (CFU/ml) were counted after the incubation period elapsed.

Statistical Analysis

[0265] Statistical analyses were performed using JMP version 14.0 (SAS Institute Inc, Cary, N.C.). The residuals between data points and predicted values were tested for normality using the Shapiro-Wilk test. Data that did not pass were transformed and the analysis was conducted on the transformed data. Simple and multiple linear regression was performed on individual experiment sets. Summary of fit from linear regression models used the adjusted R squared values and significance was determined using α=0.05. Linear regression analysis was conducted to determine any effects on [individual] nutrient composition.

Control Experiments—Zero Current Control

[0266] A control experiment was conducted at several contact times with solutions containing R. solani, fertilizer (0.5 g/L Plant Prod), and 20 mg/L of chloride but without any applied current. There was no reduction in pathogen counts, indicating that there was no physical mechanism (e.g., a filtering effect) that may have been acting to reduce pathogen counts.

Pathogen Inactivation without the Presence of Fertilizer or Chloride

[0267] FIG. 3 shows the inactivation of Rhizoctonia solani when applying a current density of 0.76 mA/cm.sup.2 without the presence of fertilizer and chloride. When the soluble fertilizer and chloride are absent and a low current density (0.76 mA/cm.sup.2) is applied there is a detectable inactivation of Rhizoctonia solani. Pathogen inactivation increased with increasing contact time (FIG. 3), with a 77% reduction after a 3-minute exposure. The pH of the solution also remained stable at ˜5.5 throughout all contact times that were tested.

[0268] The observed inactivation under these conditions (operating voltage for this experiment was ˜32V) may be due to the acidic environment in the immediate vicinity of the anodes as low pH levels causing non-enzymatic proteolysis on the mycelial sheath of Rhizoctonia solani, ultimately leading to cell death; the higher applied potential could also induce electroporation, a process by which the cell membrane becomes increasingly permeable (increasing the porosity of the cell envelope leads to leakage of cellular material) ultimately leading to loss of function and cell death; direct oxidation of polysaccharides at the anode; protein extraction (cleavage of disulfide and/or peptide bonds due to the discharge of water and dissolved oxygen molecules) at the cathode; or reductive hydrogen peroxide production at the cathode.

Inactivation of Rhizoctonia solani in a Solution Containing Chloride

[0269] In the absence of fertilizer salts, the EFC achieved complete pathogen inactivation at all but the lowest current densities (0.76 & 1.14 mA/cm.sup.2) for the 1-min contact time when chloride (20 mg/L) was present in the solution (FIG. 4A). The 20 mg/L chloride concentration was chosen as it was well below the reported phytotoxic thresholds of most crops (species specific) (Ibrahim et al., 2015) and showed efficacy in preliminary testing (data not shown). At a current density of 0.76 mA/cm.sup.2 pathogen inactivation was greatly enhanced in comparison to the previous experiment in which there was no chloride or fertilizer present (FIGS. 3 & 4A). Although, when considered in combination with the results shown in FIG. 4, it appears that a current density of 0.76 mA/cm.sup.2 while effective, may not provide the required energy to generate a sufficient amount of free chlorine to completely control pathogens. A free chlorine residual was measured and complete inactivation was achieved at a current density of 1.14 mA/cm.sup.2 after a 2-min contact time, indicating that the critical current density threshold lies somewhere between 0.76 and 1.14 mA/cm.sup.2. This result shows the EFC's ability to achieve complete inactivation with a lower contact time of 2-minutes and releasing an even lower free chlorine concentration (˜2.88 mg/L). Beyond a current density of 1.14 mA/cm.sup.2, complete inactivation was achieved by the 1-min contact time (FIG. 4A), which is expected given the relatively high free chlorine levels achieved at these current densities (FIG. 4B).

[0270] Regression analysis was used to characterize the production of free chlorine as a function of contact time and current density. Results indicate that there is a significant relationship (R.sup.2=0.60; p<0.0001) between contact time and current density. The pH was shown to respond proportionally to contact time, with pH increasing from 5.5 to as high as 8.5 at the longest contact times (data not shown).

[0271] The free chlorine residuals observed (FIG. 4B) are well beyond reported phytotoxic thresholds with a residual of ˜25 mg/L for 6.82 mA/cm.sup.2 at the 1-minute contact time. Under these solution conditions (e.g., raw irrigation water with trace chloride levels) there would be a need to include a free chlorine stripping step prior to crop application. This said, under these conditions the system could be used to generate sufficient free chlorine residuals to provide system-wide disinfection between crop cycles.

Free Chlorine Evolution with Increasing Fertilizer and Current Density

[0272] Pathogen inactivation efficacy was demonstrated in the presence of a representative commercial fertilizer. Effluent free chlorine levels at three different concentrations of commercial fertilizer were evaluated at a fixed chloride concentration of 20 mg/L in the absence of Rhizoctonia solani (FIG. 5). This chloride concentration is compatible with crop production but still provides sufficient chloride to generate phytotoxic levels of free chlorine in the absence of a free chlorine stripping step (FIG. 4B). FIG. 5 shows a positive correlation between the production of free chlorine and the contact time of the solution with the electrodes. Further, when increasing the current density there is a large increase in the amount of free chlorine produced in bulk solution when fertilizer levels are low (0 and 0.05 g/L). Although the free chlorine levels rose quickly they reach a plateau at about the 2-min contact for current densities of 6.82 and 9.09 mA/cm.sup.2 when fertilizer was not present. The data presented in FIG. 5 indicates that the concentration of effluent chlorine at lower current densities is current limited, while at higher current densities the system becomes mass transport limited. Mass transport limitation was due to depletion of chloride ions at the anode-solution interface as local supplies of chloride were transformed to free chlorine. At higher current densities the conversion of chloride to free chlorine was greater than the replenishment rate of chloride, which lead to the observed plateau (FIG. 4B; FIG. 5). When fertilizer was introduced into the test solution, even in small amounts (i.e., 0.05 g/L), the free chlorine residuals decreased by as much as two orders of magnitude (FIG. 5, middle row panels). At an application rate of 0.5 g/L, the free chlorine dropped to <1 mg/L; well below reported phytotoxic thresholds (˜2.5 mg/L).

[0273] The introduction of fertilizer clearly reduced the residual free chlorine concentrations in the test solutions (FIG. 5). Given the significant drop in free chlorine levels, even at modest fertilizer concentrations, fertility regimes should be considered when determining contact times and current densities in these types of systems. The dramatic reduction in effluent free chlorine in the presence of fertilizer indicated that there was a competing sink (in the fertilizer) for free chlorine. If the competing sink is more effective at consuming free chlorine than the pathogen inactivation mechanisms then the system would not be effective for pathogen control in typical greenhouse production systems. Conversely, the pathogen inactivation mechanisms predominated making it possible to control pathogens while taking advantage of the secondary sink present in the fertilizer to reduce the free chlorine levels below reported phytotoxic thresholds.

Rhizoctonia solani Inactivation Experiments—Pathogen Inactivation in the Presence of Fertilizer

[0274] In order to determine the influence of the competing free chlorine sinks on pathogen inactivation efficacy, Rhizoctonia solani inactivation was determined in the presence of fertilizer while increasing both chloride concentrations (FIG. 6) and current densities (FIG. 7).

[0275] When chloride concentrations were increased from 20 to 50 mg/L under the lowest current density (0.76 mA/cm.sup.2), there was a modest increase (17%) in pathogen inactivation but not sufficient to result in complete inactivation even at the 3-min contact time (FIG. 6A). Increasing the current density to 1.14 mA/cm.sup.2 resulted in complete inactivation at chloride levels 30, 40 & 50 mg/L beyond a 2-min contact time (FIG. 6A). Once again, at both current densities, the free chlorine residuals in the outflow were well below phototoxic thresholds (FIG. 6B). When increasing the concentration of reactants (chloride) at the anode surface, free chlorine concentrations in the bulk solution will increase concomitantly due to mass transport mechanisms that move the free chlorine away from the anode and into the bulk solution. Increased bulk solution free chlorine concentrations likely lead to the increased inactivation rates as more pathogen propagules would come into contact with free chlorine in the bulk solution relative to the limited anode surface area.

[0276] Free chlorine generation was monitored while maintaining constant current densities (0.76 mA/cm.sup.2 and 1.14 mA/cm.sup.2) over increasing chloride concentrations (20 mg/L to 50 mg/L) (FIG. 6B). In this scenario there was a marginal increase in free chlorine leaving the EFC. However, this increase in free chlorine generation was minimal given the 2.5-fold increase in chloride concentration (FIG. 6A). It is clear that under the conditions tested, the manipulation of other process control mechanisms (e.g., current density and contact time) are more influential in achieving pathogen inactivation.

Inactivation of Rhizoctonia solani as a Function of Current Density

[0277] Increasing the current density while maintaining a constant chloride concentration (20 mg/L) increased pathogen inactivation efficacy (FIG. 7A). As current density increased more electrons became available [at the anode surface] to participate in the reactions leading to the formation of free chlorine. As this charge transfer increased, the amount of free chlorine produced was no longer current limited; rather, it became governed by the mass transfer efficiency of the system (FIG. 4B; FIG. 5). The increased free chlorine concentration at the anode supports a greater flux to the bulk solution where it is available to further react with free-floating pathogen cells. The EFC achieved higher inactivation rates of Rhizoctonia solani after a 1-min contact time, with the exception of the lowest current density (0.76 mA/cm.sup.2) (FIGS. 4A, 6A, 7A). When increasing the current density to 1.14 mA/cm.sup.2, there was a 2.80 log reduction for the 1-minute contact time and beyond. When increasing the current to 2.27 or 3.41 mA/cm.sup.2, a 3.75 log reduction was achieved at the 1-minute contact time. A current density of 4.55 mA/cm.sup.2 achieved similar log reductions to lower current densities but inactivation was achieved in half the time (30 seconds). The highest current densities (6.82 and 9.09 mA/cm.sup.2) resulted in complete inactivation at all contact times tested.

[0278] When fertilizer is present in the test solution the effluent free chlorine residuals were consistently and considerably lower (<0.8 mg/L free chlorine) (FIG. 7B) than solutions that did not contain fertilizer (FIG. 4B) regardless of the current density applied. One of the main concerns with using free chlorine to treat irrigation water is phytotoxicity, which can occur at effluent concentrations as low at ˜2.5 mg/L. Presently, the addition of fertilizer salts, at concentrations consistent with commercial recipes, reduced effluent free chlorine to levels compatible with crop production (Cayanan et al., 2009; Ibrahim et al., 2015); yet, the addition had negligible impacts on pathogen inactivation efficacy. Even at the highest current densities and contact times achievable with the current system, the effluent free chlorine residuals still remained well below reported phytotoxic thresholds (FIG. 5). The ability to apply these high currents and/or long contact times, without the threat of exposing the crop to phytotoxic levels of free chlorine, demonstrate that even recalcitrant pathogens could be controlled through the manipulation of contact time and/or current density.

Nitrogen Dynamics in the EFC System

[0279] The reduction in free chlorine residuals in the presence of fertilizer containing ammonium (FIG. 5) suggests that breakpoint chlorination occurred during treatment. Ammonium sulphate was used as a supporting electrolyte at a concentration of 0.02 g/L, which corresponds to the total nitrogen in the 0.05 g/L fertilizer solutions used in the other experiments presented (FIG. 5). At a current density of 1.14 mA/cm.sup.2, the concentration of ammonium was inversely proportional to the contact time. However, the concentration of nitrate, which was not initially present, was also shown to be proportional to the contact time. The result was no net change in total nitrogen (FIG. 8A). At lower current densities, the conversion favoured nitrification (FIG. 8A). At higher current densities (e.g., 2.27 mA/cm.sup.2) nitrification also occurred; however, denitrification also became part of the overall process ultimately leading to a small net loss of total nitrogen from the solution. The amount of nitrogen lost from the solution increased modestly with increasing current densities (4.55-9.09 mA/cm.sup.2; data not shown).

[0280] Free chlorine was shown to variably increase between the current densities and the contact times applied to the solution when containing ammonium sulphate (FIG. 8B). However, these levels of effluent free chlorine are smaller than the amount leaving the EFC in bulk solution when no fertilizer was present (FIG. 4B). The suspected cause for this decreased effluent free chlorine with the presence of fertilizer is due to the consumption by ammonium and transformations to other nitrogenous species due to direct oxidation by the anode and indirect oxidation from free chlorine. Maintaining the pH between 5.5 and 6.5, which is compatible with crop requirements, limits the amount of nitrogen lost from the system. The surface of the anodic working electrode for RuO.sub.2 produces portions of N.sub.2, NO.sub.2.sup.− and NO.sub.3.sup.−, which are increasingly formed with higher pH and current densities. The conversion rates of these products are limited in undivided electrochemical cells, such as the one presented herein, in comparison to divided cells. Thus, the loss of total nitrogen will be limited due to the characteristics of the fertigation solution being treated and the use of an undivided cell.

[0281] At higher current densities, breakpoint chlorination has been demonstrated as the most likely mechanism for the consumption of free chlorine, while lower current densities favoured the formation of secondary reactions such as nitrate generation. Breakpoint chlorination is likely the predominant secondary sink for free chlorine in the present methods, however, the consumption of excess (beyond pathogen inactivation demand) free chlorine cannot be solely relied upon as only being caused by breakpoint chlorination. Other components in fertilizer also contribute to the consumption of free chlorine, such as ethylenediaminetetraacetic acid (EDTA), Fe.sup.2+ and Mn.sup.2+,

Nutrient Stability

[0282] Individual macronutrient ions from the 0.5 g/L fertilizer solution treated at a current density of 4.55 mA/cm.sup.2 were measured. This current density was more than sufficient to inactivate pathogens under all test conditions, yet maintained residual free chlorine levels below phytotoxic levels in the presence of fertilizer (FIG. 4A, 5, 7A). The effluent concentration of chloride was shown to decrease in proportion to the amount of free chlorine leaving the EFC, which is consistent with the expected chlorine mass balance. Less transient chloride reductions could be due to degassing (Cl.sub.2(g)), chloramination or free chlorine reacting inside pathogen cells and becoming bound. Nonetheless, the concentration of chloride in the effluent was found to be stable, demonstrating that in situ electrochemical hypochlorination continues to regenerate free chlorine while conserving chloride. All other measured nutrients were stable under the test conditions (data not shown) as determined by slope analysis (all slopes=0 at p<0.05), which demonstrated that nutrients can be conserved in this system under prescribed operational conditions.

[0283] Higher current densities and longer contact times were also tested and found to have only minor effects on select nutrient ions (NO.sub.3.sup.−, K.sup.+ & SO.sub.4.sup.2−) (data not shown). pH in the solution is regulated to control increase nitrogen loss from the fertigation solution and chloramine formation. This said, pH is routinely adjusted in production systems and at typical fertigation solution pH levels (i.e., 5.4-6.5) nitrogen should be stable. Only minor effects on macronutrient ions were noted.

Direct Operational Costs

[0284] The electrolytic power cost was considered for the 2.27 mA/cm.sup.2 current density profile (i.e., costs of ancillary equipment not included in calculations). This current density resulted in a high pathogen inactivation rate within a 1-min contact time or a flow rate of 380 mL/min (FIG. 7A), which is sufficient to accommodate a bench-scale crop production trial with a fertigation reservoir of 200 L. Under continuous operation, the current EFC configuration would use 0.447 kWh for treating 1000 L of solution. At an energy price of $0.12/kWh this translates to a treatment cost of $0.05/m.sup.3. However, the time needed for treating this volume of irrigation solution is 43.86 hours. If using a current density of 4.55 mA/cm.sup.2 at nearly double the flow rate (720 mL/min), the cost remains the same but the treatment time is reduced to 23.15 hours. These calculations are basic and do not account for additional energy and hardware costs, nor do they represent a reasonable treatment cycle.

Example 2—Boron Doped Diamond (BDD) Electrodes and Organic Fertilizer in the Electrochemical Cell System

[0285] An organic fertilizer was added into solution and treated with Dimensionally Stable Anodes (DSA) and Boron Doped Diamond electrodes. The solutions were measured for TOC (total organic carbon), TN (total nitrogen) and individual ions in solution noting the differences prior and after treatment using both technologies.

[0286] The source of ammonium and nitrate in fertigation solution containing organic fertilizer was determined and revealed possible mechanisms for the inactivation of fungi. Further it was determined that BDD electrodes can be used with an organic fertilizer. Organic fertilizers contain proteins and the degradation products (NH.sub.4.sup.+ and NO.sub.3.sup.−) are not readily bioavailable for plant growth. The proteins need to be converted to other forms through bacterial degradation, which can be problematic for various reasons. Electrochemical mineralization of these organics and releasing these ions is demonstrated herein to be a reliable resource for providing these essential ions for crop growth in the fertigation solution.

[0287] Using Dimensionally Stable Anodes there was no significant decrease for TOC and TN with the current density of 1.14 mA/cm.sup.2 for all contact times (FIG. 9). However, when increasing the current density to 2.27 and 4.55 mA/cm.sup.2, there were significant decreases with TOC and TN. The DSA's showed significant increases in calcium with current density and the contact time for all but the current density of 1.14 mA/cm.sup.2 at the 3-minute contact time (FIG. 10A). Furthermore, the analysis showed increases and decreases in phosphate and sulphate for random parameters, however none of these were found to be significant (FIG. 10A/B). However, there was a significant increase in potassium for the current density of 2.27 mA/cm.sup.2 with a 3-minute contact time and 1.14 mA/cm.sup.2 for the 2-minute contact time (FIG. 10B). No significant increases in ammonium and nitrate were found for all parameters, however, there was a significant decrease for the current density of 1.14 mA/cm.sup.2 with the 3-minute contact time (FIG. 10A). With higher current densities, there is denitrifying occurring, however, the rate of ammonium released and nitrification is counteracting the denitrification process. Although, there is still a loss of TN from the solution, ions will be released from the organics and replenish the ions that are being lost by denitrification.

[0288] With the use of BDD electrodes, there were significant decreases in TOC for every parameter, except for the current density of 1.14 mA/cm.sup.2 and a contact time of 1-minute (FIG. 11). There were no significant differences in the total nitrogen of the solution, indicating that denitrification is not active like the previous experiments conducted with DSA's.

[0289] With analyzing the ions in solution using the BDD electrodes, there were clear trends by increasing nutrients within the irrigation solution. There were significant increases in calcium, nitrate, ammonium (FIG. 12A). There were some changes in the mean for phosphate throughout the treatments. There were significant decreases in potassium for current densities with treatment (FIG. 12B). Increases by 46.55 mg/L in ammonium were found with the current density of 9.09 mA/cm.sup.2 with a 3-minute contact time (FIG. 12A). Furthermore, increases by 22.75 mg/L in nitrate were found with the same current density and contact time.

[0290] The BDD system shows compatibility with the use of organic fertilizers, as well as an ‘enhancement’ of the fertilizer.

Example 3—Boron Doped Diamond (BDD)-Based Electrochemical Advanced Oxidation Process (EAOP) and Rhizoctonia solani Inactivation in Fertigation Solutions

[0291] It was demonstrated that a BDD-based electrochemical advanced oxidation process could achieve sufficient Rhizoctonia solani inactivation rates in fertigation solutions. Further, the effects of the process on solution fertilizer composition was determined and the phytotoxic potential of the treated solution in terms of residual disinfection products (e.g., free chlorine) was established.

Materials and Methods

Pathogen Culturing

[0292] A pure culture of R. solani (AG-8) isolated from wheat was provided courtesy of Dr. Allen Xue at the Plant Pathology Ottawa Research and Development Centre (Agriculture and Agri-Food Canada).

Test Solution Preparation

[0293] The R. solani culture was vacuum filtered through 1.5 μm filter paper (Whatman 934-AH). The retained material was rinsed with deionized water to remove any residual broth remaining on the mycelia. The mycelia were weighed (TE 124S, Sartorius d=0.1 mg, Germany) to obtain the total mass of mycelia added to the solution. A concentration of 0.2 g/L of mycelia was aimed for the test solution of each experiment conducted. Mycelia were transferred to a blender (HH-362, E.F. Appliances Canada LTD, China) with 300 mL of DI water and blended for 1 minute. The suspension was then transferred to a polypropylene tank containing the irrigation test solution with fertilizer and potassium chloride added. Potassium chloride was added for selective experiments to perform electrochemical chlorination. The composition of the test solution varied between each experiment and for known test solutions is in table 1:

TABLE-US-00002 TABLE 1 Composition of irrigation solution for electrochemical treatment using the Boron-Doped Diamond electrodes Chloride Fertilizer Concentration concentration (mg/L) Fertilizer type (g/L) FIG. 14 0 Plant Prod Water Soluble 0.5 Fertilizer (20-8-20) FIG. 15 20 Plant Prod Water Soluble 0-0.5 Fertilizer FIG. 17 20 Plant Prod Water Soluble 0.5 Fertilizer FIG. 18 20 Plant Prod Water Soluble 0.5 Fertilizer

Flow Cell

[0294] The electrochemical flow cell (EFC) utilized here was described previously (Lévesque et al., 2018). In the current study, the ruthenium dioxide anodes were replaced with Boron-Doped Diamond (BDD) anodes, while the stainless-steel cathodes remained. The cell volume between the electrodes was 380 mL and the flow rates 720, 380, 190 and 127 mL./min were used for experiments. The reported contact times (in minutes) approximate the time, as a function of flow rate, that the irrigation solution is in direct contact with, or in the immediate vicinity of, the surface of the electrodes during each electrochemical treatment.

[0295] A power supply (DF1730SC 20A DC power supply, Gold Source, China) was connected to the anode and cathode terminals. Throughout each experiment the applied current and voltage were monitored. Effluent samples were collected at pre-defined times and immediately analyzed to determine pH (542, Corning, USA), and free chlorine concentration (DPD Test 'N Tube cuvette with free chlorine reagent set kit; DR/850 portable colourimeter, Hach Company, USA). Untreated samples were collected from the polypropylene tank at the start, middle and end of each experiment for fungal enumeration. This allowed for a representative estimation (mean) for the initial concentration of pathogens and nutrients that enter the system before applying a treatment. All samples were collected in 40 mL clear plastic high-density polyethylene (HDPE) vials (20120121, Richard's Plastics, Canada).

[0296] Samples were serially diluted (10.sup.1, 10.sup.2, 10.sup.3 and 10.sup.4) into glass test tubes using 500 μl of the sample from the original concentration. The samples (100 μL/plate) were then inoculated onto PDA plates with antibiotics (0.1 g/L of streptomycin and 0.05 g/L of ampicillin) and spread across the plate with a sterile metal hockey stick. The plates were placed in an incubator (Innova 4340, New Brunswick Scientific, USA) at 30° C. for 48 hours under 58 μmol/m.sup.2 of light on a 12 h photoperiod. Colonies were counted after the incubation period to determine the survival rate of pathogens following the electrochemical treatment.

Nutrient and Perchlorate Analysis

[0297] Individual macronutrient ions from the fertilizer solution were measured with a Shimadzu HPLC system equipped with a DGU-20A3 degasser, a SIL-10AP autosampler, two LC-20AT pumps, two CDD-10A VP conductivity detectors, CTO-20AC column oven, and CBM-20A system controller. Total nitrogen was measured using a Shimadzu TOC analyzer with a total nitrogen component attachment (TNM-1, Shimadzu Scientific Instruments, USA). Perchlorate was analyzed following according to Uchikawa (1967). Samples containing fertilizer could not analyzed for perchlorate due to interference with nitrate (Uchikawa, 1967).

Statistical Analysis

[0298] Statistical analyses were performed using JMP version 14.0 (SAS Institute Inc, Cary, N.C.). Data was tested for normality using the Shapiro-Wilk test. Data sets failing the Shapiro-Wilk test were transformed and the analysis was conducted on the transformed data. Summary of fit from linear regression models used the adjusted R squared values and significance was determined using a=0.05. Linear regression analysis was conducted to determine any effects on [individual] nutrient composition.

Pathogen Inactivation in the Absence of Fertilizer or Chloride Salts

[0299] When only R. solani is present in deionized water, a low current density of 1.14 mA/cm.sup.2 resulted in a moderate decrease in culturable R. solani (FIG. 13). When the contact time of the solution was increased to 6-minutes, there was a log reduction of 3.65 in R. solani from an initial concentration of 6666±850 CFU/mL. Increasing the current density to 2.27 mA/cm.sup.2 resulted in a log reduction of 3.80 at the same six-minute contact time. The major factor contributing to the inactivation of pathogens is by indirect oxidation by ROS (H.sub.2O.sub.2, O.sub.3, O2.sup.−) in the bulk solution. The most powerful ROS (OH) is a major factor for disinfection.

[0300] The combination of all ROS causes damage to the cell membrane, which ruptures and releases cell constituents leading to inactivation. This combination of ROS that are contributing to inactivation rates offers explanation for the efficacy of electrochemical disinfection in removing the majority of pathogens. Although, there are some additional factors that should be considered with electrochemical disinfection. Reductions can also be explained by the acidity at the vicinity of the anodes causing structural changes to the mycelial sheath, which can cause cleavage of essential proteins. There is also the possibility of increased permeability of the mycelial membrane due to electroporation, which leads to leakage of intracellular contents into solution. It must be noted that although the current densities used for the experiment were low, the voltages where found to be high due to the absence of a supporting electrolyte. The voltage was found to vary ˜15 V with 1.14 mA/cm.sup.2 and 32 V with a current density of 2.27 mA/cm.sup.2.

Pathogen Inactivation in the Presence of Fertilizer Salts

[0301] Pathogen inactivation efficacy was evaluated in solutions containing fertilizer salts but no added chloride. In comparison to the results shown in FIG. 13, when applying 1.14 mA/cm.sup.2 for a contact time of 6-minutes the inactivation of R. solani is partially inhibited by the presence of fertilizer in solution, which reached a log reduction of 3.58 CFU/mL. There was a reduction in inactivation rates by 22% (with 1.14 mA/cm.sup.2) when fertilizer was present in solution in comparison to when fertilizer was absent (FIGS. 13 and 14). This result consistently follows with the same contact time (6-minutes) but increasing the current density to 2.27 mA/cm.sup.2 by achieving a log reduction of 3.54. This decrease in log reduction equates to a reduction in inactivation rates by 33% with the presence of fertilizer in solution. When increasing the current density to 4.55 mA/cm.sup.2, inactivation rates increase to a log reduction of 3.67 CFU/mL for the 6-minute contact time. Further increasing the current density to 6.82 and 9.09 mA/cm.sup.2 reached log reductions of 3.66 CFU/mL for the former and 3.68 CFU/mL for the latter between 0 and 6-minute contact times. The rate of R. solani inactivation is likely caused by competing reactions with components present in the fertilizer. The fertilizer can act as a sink for produced disinfectants in solution and fertilizer components can compete with reactions for inactivating R. solani by hydroxyl radicals and other ROS. Nonetheless, the presence of a commercial fertilizer reduced the inactivation rates of R. solani, it did not completely inhibit the system from inactivating pathogens (inactivated 64% of pathogens). Additional oxidants, such as free chlorine, may be added to achieve the complete inactivation of R. solani.

Chloride Addition Experiments: Free Chlorine and Perchlorate Evolution

[0302] Free chlorine in the flow cell effluent was monitored while treating solutions containing 20 mg/L of chloride, added as potassium chloride (KCl), over a range of current densities, contact times and fertilizer concentrations (FIG. 15; Table 1). Without fertilizer present, the concentration of free chlorine tended to increase with contact time and current density (FIG. 15). The concentration of free chlorine increased with current density but plateaued at about 2 mg/L beyond a contact time of 2-minutes for current densities of 6.82 and 9.09 mA/cm.sup.2. The saturation point for these current densities and contact times suggests the process reached a physical or electrochemical limit; a limit most likely mass transport related. The efficiency of BDD electrodes for producing hydroxyl radicals and further oxidizing chlorinated products (e.g. ClO.sup.−) can lead to the formation of chlorates and perchlorates (Sirés et al., 2014). The comparatively (i.e., relative to DSAs designed for free chlorine production) low concentration free chlorine from the EFC may be in part due to the formation of chlorate species, which are not measured via the DPD free chlorine method used. When fertilizer is present in solution, the effluent-free chlorine concentration decreased to <0.25 mg/L for all current densities and contact times (FIG. 15).

[0303] The EFC system outfitted with BDD electrodes has the potential to form chlorate species. Perchlorates are particularly harmful to human health and this compound can be assimilated by crops which is species specific, but may pose a risk for consumers such that perchlorate should be monitored while only permitting concentrations under regulatory standards. Analysis of perchlorates (fertilizer free solutions only) showed that perchlorate remained below 2 μg/L (FIG. 4), which is below safe drinking water limits in all jurisdictions examined (e.g., United States EPA limit 24.5 μg/L). Perchlorate was the only chlorate species examined in the current study. Additional chlorate species may be examined. The formation of chlorate and perchlorate requires the production of hypochlorite as an intermediate species. Thus, if the pH of the solution is maintained at more acidic conditions with low current densities, this will limit the formation of chlorates. Also, the presence of fertilizer can act as an inhibiting factor to the formation of chlorates and perchlorate due to more competing reactions at the surface of the anodes. This process for competing reactions is similar to preventing the formation of chlorates by increasing the concentration of chloride. There are also additional electrochemical mechanisms that can remove chlorates by reduction reactions, which returns chlorates back to chloride and oxygen. These operational methods can all be used to prevent or remove chlorates in solution as precautionary measures with the EFC if desired.

[0304] Adding chloride to the fertigation solution further increased the inactivation rate of R. solani (FIG. 17A). When applying a current density of 1.14 mA/cm.sup.2 with a contact time of 3-minutes, there was a 69% reduction of R. solani (CFU/mL). When increasing the current density to 2.27 mA/cm.sup.2 with the 2-minute contact time, there was a decrease by 99.95% of pathogens in solution. For the same current density, but with the increased contact time of 3-minutes, R. solani was completely inactivated. When applying 4.45 mA/cm.sup.2, an inactivation rate of 99.98% was achieved for the 2-minute contact time. Increasing the current density to 6.82 mA/cm.sup.2, gave the same inactivation in half the time (1-min CT). The highest current density tested (9.09 mA/cm.sup.2) gave an inactivation of 98.95% at a 0.5-minute contact time and complete inactivation at a 1-minute contact time. Inactivation efficiency improved considerably when 20 mg/L of chloride was introduced, as KCl, to the fertigation solution (FIG. 17A). However, in comparison to previous research with DSA electrodes, the required current density is higher (9.09 mA/cm.sup.2 for BDD vs 6.82 mA/cm.sup.2 for DSA) and the contact time is twice that required for RuO.sub.2 DSA (1-minute for BDD vs 30 seconds for RuO.sub.2 DSA).

[0305] The free chlorine evolution from BDD electrodes was also monitored to ensure that the system would not release a concentration of free chlorine above the phytotoxic threshold for most major crops (2.5 mg/L) (FIG. 17B). The effluent free-chlorine concentration does not follow a consistent trend with increasing the contact time and current density of the system. However, the main aspect is that all measured values are considerably lower than the phytotoxic threshold.

Plant Nutrient Dynamics

[0306] The individual ions comprising the fertilizer solution were monitored pre- and post-treatment at a current density of 9.09 mA/cm.sup.2 (FIG. 18). No differences were detected for phosphate, sodium, potassium, magnesium, and calcium. Chloride showed a significant decrease with contact time, which is consistent with the pseudo-first-order kinetics governing the formation of free chlorine species. Chloride had decreased by 2.99±0.16 mg/L with a current density of 9.09 mA/cm.sup.2 and a contact time of 1-minute and decreased by 7.69±0.13 mg/L for 3-minutes. Several ions increased slightly after a 3-minute treatment. There were significant increases between the 0 and 3-minute contact times in nitrate by 6.35±0.28 mg/L (p=0.0078), ammonium by 5.32±0.63 mg/L (p=<0.0001), and sulphate by 1.72±0.43 mg/L (p=<0.0001) (FIGS. 18A-B). The increase in nitrate may be due to the direct and/or indirect oxidation of ammonium (Benito et al., 2017). The increases in sulphate could be attributed to the oxidation of trace amounts of sulphide or sulphur containing amino acids such as cysteine and methionine). An alternative source of these ions could be from the degradation of proteins and subsequent deamination of amino acids. The deamination of amino acids has been known to occur in the presence of radical species. The reactions are catalyzed by copper ions, which were present in trace amounts in the fertilizer used in the experiment. The increase in nitrate, ammonium and sulphate is supported by the decrease of non-purgeable organic carbon (NPOC) when only the pathogen and deionized water are present in solution (FIG. 19A). The decrease in NPOC indicates that dissolved components in solution that originated from the pathogen are being mineralized. When mineralization occurs, this will release CO.sub.2 as well as other ions that were shown to increase with EAOP due to the action of OH.sup.−. These increases in essential ions were statistically significant (FIGS. 19B-C).

[0307] Applying a low current density (2.27 mA/cm.sup.2) without the presence of fertilizer or chloride in solution can inactivate 95% of R. solani. Complete inactivation was achieved with the presence of fertilizer and 20 mg/L of chloride in solution. Complete inactivation of R. solani can be achieved electrochemically using BDD anodes and stainless-steel cathodes at a current density of 2.27 mA/cm.sup.2 and contact time of 3-minutes. However, the contact time required for complete inactivation can be reduced through a concomitant increase in current density, with 9.09 mA/cm.sup.2 achieving complete inactivation after 1-minute when fertilizer and chloride are present. The complete inactivation of R. solani was achieved while maintaining acceptable nutrient balances and without a build-up of free chlorine beyond reported phytotoxic thresholds. Perchlorate generation was a concern; however, the concentration remained below accepted drinking water quality standards in the absence fertilizer. Many essential nutrients for plant growth were shown to remain constant with reaching complete inactivation (9.09 mA/cm.sup.2+fertilizer+chloride). Increases in these nutrients were shown for the ions ammonium, nitrate and sulphate. The decrease in NPOC when only the pathogen is present in solution suggests the mineralization of dissolved components are releasing these nutrients.

Example 4—Greenhouse Floriculture Production of Cyclamen persicum in the Presence of Fusarium oxysporum. Using Treated and Recirculated Nutrient Solution

[0308] A randomized complete block design was arranged with 5 treatment levels (troughs) on each grow bench (both controls set up in front of one grow bench) (FIG. 20A, 20B). Each grow bench was nested with all five treatments having a positive control, negative control, ozone, AOP, and DSA. The negative control was not inoculated with F. oxysporum in solution, while the positive control, ozone, AOP and DSA treatments did contain the inoculum. A water-soluble fertilizer (20-8-20, Master Plant Prod Inc., Canada) was added for each treatment at a concentration of 0.5 g/L in each reservoir. The irrigation system was arranged by drip irrigation with spikes inserted in the soil and the solution was recirculated back towards reservoirs during the whole production cycle (FIG. 21). Each water treatment system was evaluated for pathogen inactivation and quality of plants after 6 weeks of growth.

Pathogen Inactivation

[0309] Pathogen inactivation was monitored for all treatments within the first pass from reservoir 1 towards reservoir 2. F. oxysporum was found to be relatively unchanged from passing between reservoirs for the positive control. Indicating that stable colonies are passing through the irrigation system and reaching ornamental crops. The negative control treatment did not detect external fungal pathogens in the fertigation water, which determines that effects on crop growth was solely caused by the inoculated pathogen. All water treatment technologies used for disinfection was shown to achieve the complete inactivation of pathogens in fertigation solutions.

Plant Health

[0310] After 6 weeks of growth, all treatments exhibited significant differences in comparison to the positive control for leaf area, number of leaves, petiole length and dry weights of C. persicum (FIG. 22). In comparison to the negative control, all water treatment technologies were not found to have significant differences in plant growth. Furthermore, no visual differences were observed between water treatment technologies, though, clear differences in the health of plants was discerned with the positive control due to pathogenicity (FIG. 23).

Nutrients

[0311] Following treatment with DSA's, nutrients were shown to remain relatively stable with respect to plant uptake over time (FIGS. 24-26). The only nutrient that was shown to decrease was iron, which is expected due to the oxidation of the chelating agent EDTA (FIG. 27). Precipitation of iron from solution is a known effect following oxidation methods and it was experienced by all treatment systems. DSA's have been known to destroy EDTA with preferential conditions (pH>7, high [Cl.sup.−]), although, a long contact time of ˜50 minutes is needed to fully destroy EDTA using a low current density. In cases, there was no EDTA that was removed in solution when the pH of the solution is less than 7. DSA's was shown that iron will be depleted over time, though, it may remain stable in solution for longer periods in comparison to ozonation and AOP treatments.

Example 5 Fertigation Water Treatment with Deep Water Culture (DWC) Lettuce

[0312] Three experiments were performed, each experiment was conducted over a total period of 2 weeks with consecutive treatments being applied 5 times per week (Monday-Friday). A schematic of the randomized block design is shown in FIG. 28A while a photograph is shown in FIG. 28B. Experiment 1 (DSA+NH.sub.4.sup.+) used a soluble fertilizer mix at 0.5 g/L (10561, 20-8-20 Master Plant-Prod Inc., CA), 42 mg/L Ca.sup.2+ (Ca(NO.sub.3).sub.2) and 20 mg/L of Cl.sup.− (KCl) in solution. The solution was passed through the EFC system and returned to each reservoir following treatment, including the control group. Experiment 2 (DSA+NH.sub.4.sup.++UV) used the same fertigation solution and EFC treatment methods, although a UV disinfection system (GAUV-6SM, Greenway Water Technology, CA) was added at the effluent of the EFC. The volume of the UV chamber was 1.5 litres, which provided the solution with a 10-minute photolysis period with using the same flow rate of 720 mL/min. The control group was not subjected to electrochemical treatment but was treated using UV disinfection. Experiment 3 (DSA+NO.sub.3.sup.−) followed the same treatment procedures as Experiment 1 however, the fertilizer solution was replicated using chemical standards (Thermo Fisher Scientific, CA) only replacing NH.sub.4.sup.+ with NO.sub.3.sup.− in solution. The three different experiments were conducted because conventional hypochlorination has been shown to have negative impacts on plant growth when HOCl reacts with ammonium (NH.sub.4.sup.+), which forms phytotoxic molecules called chloramines (NH.sub.2Cl, NHCl.sub.2 & NCl.sub.3) or also called combined chlorine (CC). Tertiary treatment techniques such as UV disinfection provides an approach for diminishing the concentration of chloramines through photodecomposition. Another alternative approach such as using a nitrate (NO.sub.3.sup.−) based fertilizer, without the presence of NH.sub.4.sup.+, entirely prevents the formation of chloramines in solution.

Microbial Inactivation

[0313] Microbes were not inactivated in the control treatment for experiments conducted with a fertilizer containing ammonium and/or nitrate, though, some microbes were inactivated following UV treatment (FIG. 29). When applying a current to the solution, microbes were inactivated in large part of the effluent solution with the current density of 2.27 and completely inactivated with using 4.45 mA/cm.sup.2. The bulk solution contained more microbes but were reduced at least 100-fold with treatment of the fertilizer solution without UV. The number of microbes in bulk solution was higher with the UV treatment because the added treatment degraded the produced disinfectants (FIG. 30). Without the release of residual disinfectants, the microbes were able to survive in solution.

Plant Production Quality

[0314] Electrochemical treatment of the fertigation solution in Experiment 1 was shown to cause phytotoxic effects to lettuce grown in DWC (FIG. 31A). A decrease in root biomass and root browning was apparent when treated with 2.27 mA/cm.sup.2, while the roots in 4.55 mA/cm.sup.2 were scarce and nearly un-present. The overhead biomass was also notably smaller with increasing current density. With the addition of UV disinfection in Experiment 2, the root and shoot biomass were more comparable between treatments in comparison to plants in Experiment 1 (FIG. 31B). Nonetheless, EFC treatments did experience morphological changes with higher amounts of lateral branching of seminal roots in comparison to the control group. Experiment 3 demonstrated little to no visual differences between treatment groups for both the shoot and root biomass (FIG. 31C). These observations are also reflected in the provided data which measured the growth parameters (FIGS. 32A-32E). Remarkably, the treatment 2.27 mA/cm.sup.2 had a 13% increase in overhead biomass in comparison to the control.

Example 6 Organic Fertilizer Decomposition and Nutrient Solubilization Solution Preparation

[0315] The test solution was prepared in a 60-litre polyethylene container by adding 0.5 g/L of a powdered organic fertilizer (9-1.5-7 EZ-GRO, Canada) (Table 1) to deionized water. Experiments conducted with the electrochemical flow cell (EFC) using DSA anodes also received 10 mg/L of chloride (Cl.sup.−) by adding potassium chloride (KCl). No additional chloride was added for ozonation, AOP and electrochemical treatment with BDD anodes. The solution was constantly mixed using a magnetic stirrer to ensure homogeneity of the fertilizer. The solution was treated by all four technologies at various contact times and analyzed for changes in solution chemistry and nutrient availability for plant growth.

Nutrient Solution Analysis

[0316] The solution's turbidity had decreased by 82 NTU following the treatment time of 60 minutes with BDD electrodes, while DSA's decreased by 76 NTU (FIG. 33). This is also reflected by the decreases in Non-Purgeable Organic Carbon (NPOC), which decreased by 282 mg/L following treatment with BDD and only 56 mg/L with DSA (FIG. 34A). This shows that organic components are being mineralized and releasing ions which become solubilized in solution. Furthermore, the total nitrogen (TN) of the solution also increased by 23 mg/L following treatment with BDD electrodes at the 20-minute treatment time (FIG. 34B). Electrochemical treatment with DSA's exhibited decreases over treatment time, which results from breakpoint chlorination reactions in denitrifying the solution.

[0317] The electrochemical treatment with BDD electrodes was shown to have the highest release of nutrients compared with all other systems. The degradation of organic components following treatment with BDD released phosphate (12 mg/L), ammonium (26 mg/L), nitrate (81 mg/L), and calcium (12 mg/L) (FIGS. 35-37). Other nutrients were shown to remain stable in solution following treatment. DSA's release ions to a considerably smaller extent for phosphate (6 mg/L) and calcium (4 mg/L). Furthermore, DSA's were not shown to release significant amounts of ammonium and nitrate following treatment, which is due to denitrification reactions that negate the release of nitrogen species in solution.

Example 7 Electrochemical Treatment of Fertigation Water to Break Down Contaminants

[0318] Culturing Lemna minor

[0319] A sterile culture of Lemna minor was obtained from the laboratory of Dr. Ryan Prosser (University of Guelph, School of Environmental Science). The culture was transferred to a 1 L Erlenmeyer flask containing a ½ strength Hoagland solution. The cultures were transferred to a growth chamber and were left for a growing period of 7 days. After the growth period, the Erlenmeyer flasks were brought to the lab to use the healthy plants for bioassay and water treatment experiments.

Growth Chamber Conditions

[0320] The temperature and humidity sensors were built in house by the Controlled Environment Systems Research Facility (CESRF) at the University of Guelph. The growth chamber conditions for humidity and temperature were recorded using an Acer Aspire 7750 laptop (P7YEO, Acer, Taiwan) and using the Termite software for data logging (version 3.4). The temperature was maintained at 25.68±0.02° C. and the relative humidity was 38.34±0.05%. Lumigrow pro 325 LED lights (LU60001, Lumigrow, USA) were used at a 80:10:10 ratio of Red:Blue:White as overhead lighting for plants (FIGS. 38A & 38B). Furthermore, a grid system inside the growth chamber with 36 grid boxes were used to place Erlenmeyer flasks in a completely randomized design (FIG. 38C). Each ‘grid’ was measured for photosynthetically active radiation (PAR) using a modular spectrometer (USB2000+, Ocean Optics Inc., USA). This allowed to account for random differences attributed to light intensity within the growth chamber. A heat map is generated with this information and in the middle of the ‘grid box’ there was a maximum intensity of 100 μmol/m.sup.2 (FIG. 39).

Determining the Lowest Observable Effect Concentration (LOEC)

[0321] The analysis of dose-response curves for affecting the growth of Lemna minor was determined using the ‘drc’ package (v. 3.0-1, Christian Ritz, 2016) in the statistical program RStudio (v. 1.0.153, RStudio Inc., USA). The program was used to determine the EC 50 for each measured parameter for plant health and reproduction of the number of plants, number of fronds, and the dry weights of plants contained in each flask.

Electrochemical Treatment of Chemical Standards

[0322] Initial water treatment was performed by treating the solution by batch cell using the DSA and BDD anodes, as well as stainless steel (SS) cathodes. The experiment used a 2 L beaker and filled the beaker with 1.8 L of deionized water and dissolved the chemical standards glyphosate (45521, Sigma-Aldrich, USA) or paclobutrazol (46046, Sigma-Aldrich, USA) for separate treatments. The solution was constantly mixed using a magnetic stirrer (220T, Fisher Scientific, Canada) and bar during treatment with chemical standards. Samples containing glyphosate and paclobutrazol standards were submitted to the Agriculture and Food Laboratory (University of Guelph) to quantify samples using LC-MS/MS. The mean quantifiable limit for the analytical method was 8 μg/L for glyphosate, AMPA, and paclobutrazol. The non-purgeable organic carbon (NPOC) and total nitrogen (TN) of the solution were determined using a Shimadzu TOC-Vpn & TNM-1 analyzer. A calibration curve (R.sup.2=0.99) was produced before performing the sample analysis using TOC and TN standards.

Chlorination with BDD Electrodes on Lemna minor

[0323] Chlorination was performed with BDD anodes and SS cathodes by passing a solution with 20 mg/L of chloride and deionized water through an electrochemical flow cell (EFC). The flow cell configuration was performed using the same equipment (FIGS. 40A-40D) as previous experiments with R. solani described herein. The solution was then collected and fixed to 75 mL inside an Erlenmeyer flask with a matching 75 mL of full-strength Hoagland solution. The experiment was performed in triplicate and placed inside the Grid box for further analysis.

[0324] With reference to FIGS. 32B-32D, the electrochemical flow cell (EFC) system used consisted of a set of six RuO.sub.2 dimensionally stable anodes (DSA) (De Nora Tech, Concord, USA) and a complementary set of five stainless steel cathodes, spaced 2 mm apart, in an acrylic casing. The total area of the anodes was 1320 cm.sup.2. Solutions entered the cell from the bottom, passed upwards through the electrodes, and exited the cell at an outflow port at the top of the housing. A power supply (DF1730SC 20A DC power supply, Gold Source, China) was connected to the anode and cathode of the flow cell. The applied current value was derived from the voltage drop measured across a precision current resistor (RS-50-100, RIEDON, Alhambra, Calif.) using a multimeter (Fluke 189, Fluke Corporation, Canada). A second multimeter (Fluke 87, Fluke Corporation, Canada) connected directly to the anode and cathode of the cell measured the applied voltage. A second multimeter is connected directly to the terminals of the anode and cathode array to measure the applied voltage. A variable speed peristaltic pump (Cole-Parmer 1-100 RPM) drew water from the test solution reservoir to the entry port located at the base of the flow cell.

[0325] The total free volume of the EFC, the internal volume of the housing less the volume of the electrode assembly, was 380 mL but can be adjusted. The targeted contact times were achieved by adjusting the flow rates through the cell such that a given volume of solution would remain in contact with the electrodes for the desired time interval.

Water Treatment Methods with Commercial Pesticides

[0326] Water treatment for the recalcitrant organic pollutants (glyphosate and paclobutrazol) was performed by ozonation (O.sub.3(aq)), AOP, DSA and BDD. The irrigation solution was spiked with 7 mg/L of glyphosate (Glyfos™, FMC corporation, USA) and 3 mg/L of paclobutrazol (Bonzi™, Syngenta Canada Inc., Canada) in multiple 20 L buckets containing 10 L of deionized water. Ozonation was performed with a batch reactor that was built in house at the CESRF (FIG. 40A). The batch reactor consisted of an oxygen concentrator (AS013-5, .sup.Airstep Corporation, USA), ozone generator (CD1500P, Clearwater tech., USA), PVC pipe (1.8 m×12 cm) and a 60 μm pore air stone diffuser at the base. The ozone gas stream that was injected into the batch reactor was measured by a high concentration ozone analyzer (Mini-Hicon, IN USA, USA). The ozone off gas was also measured by the ozone analyzer after removing the water vapour using the Sample conditioning system (SC-010-R, IN USA, USA). The ozone off gas from the solution was also carried out to the ozone destruct system (OCD-11, Clearwater tech., USA) after passing through the ozone analyzer. Furthermore, ozone was maintained at ˜5 mg/L O.sub.3(aq) in solution and verified using Ozone AccuVac® Ampules (2518025, Hach Company, USA) and a colourimeter (DR/850, Hach Company, USA). Once the ozone is injected in solution to the desired level, the solution was then allowed to stand for 20 minutes.

[0327] The AOP treatment was performed following ozonation with the batch reactor by opening a check valve and allowing the irrigation solution to flow through a UV chamber (model #, Greenway Water Technologies, Canada) by gravity at 310 mL/min (FIG. 40A). The desired flow rate through the UV chamber was determined by measuring the effluent for ozone using ozone ampules and colourimeter. The flow rate was adjusted until no residual ozone could be measured in solution.

[0328] The electrochemical treatments used DSA and BDD anodes with SS cathodes for both treatment methods. The EFC was configured as shown for example in FIGS. 40B-40D. The solution also added 20 mg/L of Cl.sup.− in the form of KCl. The flow rate and current densities used were performed as described herein.

[0329] All solutions were treated with the four different water treatment methods and 75 mL of effluent solution was collected and added in 250 mL Erlenmeyer flasks. Negative control samples only contained 75 mL of deionized water, while all other treatments (positive control, Ozone, AOP, DSA, and BDD) contained 75 mL of the treated and non-treated solution. In a separate 3-litre beaker, a full-strength Hoagland solution was prepared and mixed with a magnetic stirrer (220T, Fisher Scientific, Canada). For each of the Erlenmeyer flasks containing the treated solutions, 75 mL of the Hoagland solution was added into each flask. The dilution factor with the Hoagland solution resulted in a half strength Hoagland solution for plant growth. Lemna minor that were previously cultured and acclimated to the ‘Grid box’ were then added to each flask. Two Lemna minor plants with three fronds each were added to flasks for the experiment. All 5 treatments contained 3 Erlenmeyer flasks giving a total of 18 flasks with 36 Lemna plants and the experiment was performed in triplicate. All of the flasks were placed at random inside the growth chamber within each grid and recorded their location. The pH and electrical conductivity of the solutions were also measured after the 7-day growth period.

Statistical Analysis

[0330] Statistical analyses were performed using JMP version 14.0 (SAS Institute Inc, Cary, N.C.). The residuals between data points and predicted values were tested for normality using the Shapiro-Wilk test. Residuals that did not follow a normal distribution were transformed and the analysis was conducted on the transformed data. One-way ANOVA was used to determine the significance between treatments, with the significance of α≤0.05. All graphs used the calculated mean of samples within treatments with the standard error of the mean used for error bars.

Lemna Bioassay

[0331] When performing the bioassay on Lemna minor, the number of plants, fronds, and the final dry weights showed to decrease with increasing concentrations of glyphosate with respect to additional surfactants contained in Glyfosm. Significant differences were only observed at the concentration of 15 mg/L of glyphosate for the final number of fronds and the dry weight of plants (FIGS. 41A & 41B). Although, significant decreases in the number of plants were observed with glyphosate concentrations of 2.5, 5 and 15 mg/L in solution (FIG. 41A). Noticeable differences such as the number of plants, lighter colour of fronds, and spindly roots can be visualized in comparison with the control (FIG. 42A) to the presence of 15 mg/L of glyphosate (FIG. 42B).

[0332] When performing the same bioassay using paclobutrazol (Bonzi™), the results showed more profound effects on the growth and reproduction of Lemna plants. Significant decreases were observed for all tested concentrations in comparison to the control group with all of the tested parameters for plant physiological and reproductive health (FIGS. 43A & 43B). These visual differences can be observed in FIGS. 44A & 44B, showing the plants growing over top of each other and causing very spindly roots, which ultimately effects the growth of the plants.

[0333] Significant differences for all measured parameters in the health of Lemna minor was between 5 and 15 mg/L for glyphosate, while paclobutrazol had significant differences at even the lowest concentration of 0.05 mg/L. An analysis of dose-response for determining the EC50 dose with glyphosate was ˜9 mg/L using the data from FIG. 4. However, the chosen dose for foregoing experiments was slightly lowered to 7 mg/L to be equivalent to 170 times higher than the background ratios typically found in surface water in Ontario, Canada. This allows to test the system as per the worst-case scenario if poor spraying management was utilized by a neighbouring grower. With paclobutrazol, the dose-response analysis determined that the EC50 concentration was 0.01 mg/L using the data collected from FIGS. 43A & 43B. However, the concentration was increased to 3 mg/L as per the worst-case scenario that a high concentration entering surface water due to the foliar application. The foliar application of paclobutrazol can range anywhere between 1-200 mg/L. However, it must be considered that these levels will be 60 times higher than what is typically found in surface water ponds. This enables to test all of these systems for handling the worst possible scenario that a grower might experience in their agricultural career.

Electrochemical Degradation of Agrichemicals

[0334] The degradation of both glyphosate (8.5 mg/L) and paclobutrazol (12 mg/L) was conducted with the use of electrochemical systems for a direct comparison on their efficacies in a batch cell configuration. When applying a current density of 2.27 mA/cm.sup.2 with the presence of glyphosate, the NPOC and TN were shown to significantly decrease with contact time by both electrochemical systems (FIG. 45). The NPOC had decreased by 16.18%, while the TN decreased by 85.97% with the use of DSA electrodes. Furthermore, the NPOC decreased by 19.73% and the TN decreased by 32.61% with BDD electrodes with the same compound. For paclobutrazol, the NPOC was unaffected and the TN decreased by only 7.12% with the DSA electrodes. However, the NPOC significantly decreased by 18.41%, as well as the TN decreasing by 22.58% when BDD electrodes were utilized. The NPOC and TN had larger decreases between the 3 and 6-minute contact time with the DSA electrodes for glyphosate, while the changes were more subtle using BDD electrodes. Although with the presence of paclobutrazol, there were larger decreases in NPOC and TN exhibited with the BDD electrodes.

[0335] With the same standards in solution from FIGS. 46A & 46B, there were significant decreases with both systems for glyphosate and paclobutrazol when applying the same current density of 2.27 mA/cm.sup.2. The DSA electrodes removed glyphosate and AMPA from the solution to levels below the detection limit (<8 μg/L) between the contact times of 0 and 6-minutes (FIG. 46A). BDD electrodes achieved a reduction of 72.47% of glyphosate but increased AMPA by 0.10 mg/L. Although, when paclobutrazol was present, there was a reduction of 28.29% with DSA's and a reduction of 80.94% with BDD electrodes (FIG. 46B).

[0336] The complete degradation of glyphosate (<8 μg/L) was achieved using DSA electrodes with a current density of 2.27 mA/cm.sup.2 and a contact time of 6-minutes (FIG. 46A). The system was shown to have degradation, which is supported by the decrease of 16% in NPOC and 86% in TN (FIG. 45). This indicates that not only is glyphosate being degraded, but also the derived compounds sarcosine and AMPA, which were being further degraded by losing their amine groups and releasing nitrate. Furthermore, the loss of TN was due to the reduction in nitrate to ammonium and forming chloramines, which reacts with hypochlorite and denitrifies from solution. This reaction is largely dependent on the pH and the ClO.sup.−/NH.sub.4.sup.+ molar ratio to completely remove nitrogen from the solution. The final pH of the test solution was ˜6.5 with a current density of 2.27 mA/cm.sup.2 with a contact time of 6-minutes.

[0337] With BDD electrodes, the system achieved a degradation of 72% for glyphosate with the same current density and contact time of 6-minutes (FIG. 46A). The NPOC and TN showed a moderate decrease in solution, indicating that the current efficiency is lower for removing glyphosate in comparison to DSA electrodes. Glyphosate was not completely removed from solution with BDD electrodes showing 20% with 2.27 mA/cm.sup.2 (FIG. 45). Furthermore, AMPA was shown to increase from 0.009 to 0.11 mg/L and the TN in solution had only decreased by 32%. This indicates that glyphosate is being degraded at a low current density, however, the mass balance between the release and degradation of AMPA may favour its accumulation in the solution. A higher current density and pH is established for the complete removal of glyphosate and AMPA to favour mineralization and denitrification reactions.

[0338] With the presence of paclobutrazol in solution, the results were found to be opposite from what was presented with the degradation of glyphosate. The DSA electrodes showed to have a minor effect by decreasing the TN by 7% and having no significant effect on decreasing NPOC (FIG. 45). The small decrease in TN indicates that there is degradation occurring at the location of the heterocyclic compound triazole in paclobutrazol, which is supported by the results shown in FIG. 46B. The DSA electrodes removed 28% of the paclobutrazol in solution. NPOC remained unaffected which indicates that the system was unable to reach complete mineralization of the contaminant.

[0339] Degradation of paclobutrazol by BDD electrodes was shown to be more efficient in comparison to the DSA electrodes (FIG. 46B). The loss of 18% of the NPOC and 23% of TN indicates some mineralization of the compound in solution. Resulting in an 81% reduction of paclobutrazol in solution (FIG. 45). The increased destruction of this molecule was due to a combination of direct oxidation by electron transfer, discharge of water molecules to form adsorbed hydroxyl radicals, indirect oxidation by other reactive oxygen species (ROS), and organic radical intermediates. The production of hydroxyl radicals differentiates both electrochemical systems for the degradation of paclobutrazol. This process explains why BDD electrodes were more effective at removing paclobutrazol. Although both systems did not completely remove paclobutrazol, they did cause a significant reduction when comparing the initial concentration (which was used at concentrations many fold higher than environmental background levels). Both systems improve water quality for plant growth when paclobutrazol is found in trace amounts in irrigation water.

Effects of Chlorination with the Use of BDD Anodes

[0340] The effects of free chlorine and other chlorinated species formed such as chlorates and perchlorates were explored to evaluate potential effects on plant growth with BDD anodes. The health and reproduction of the plants were evaluated in relation to the current density applied to the solution. Significant decreases were observed with the number of fronds with current densities ≥3.42 mA/cm.sup.2(FIG. 47A). However, significant decreases in the number of plants and dry weights were not observed until reaching current densities of ≥4.55 mA/cm.sup.2 (FIGS. 47A & 47B). When observing the concentration of free chlorine exiting the cell, there was a positive trend for increasing free chlorine with current density (FIG. 48). However, a saturation point was reached at both current densities of 3.41 and 4.55 mA/cm.sup.2 and a moderate decrease was shown for preceding currents.

[0341] Results shown in FIGS. 47A & 47B demonstrate that no effects on plant growth or function occur with current densities≤2.27 mA/cm.sup.2. No difference in dry weight and number of plants were observed with a current density of 3.42 mA/cm.sup.2, there was however, a moderate decrease in the number of fronds (FIG. 47A). The concentration of free chlorine was shown to peak at ˜1.75 mg/L for both these current densities (FIG. 47A). These minor effects that are experienced, relate to free chlorine concentrations approaching the determined phytotoxic threshold (2.5 mg/L) for most major crops. Though, when increasing the current density ≥3.42 mA/cm.sup.2, there were clear decreases in the form and function of plants (FIG. 47A/B). The level of free chlorine had moderately decreased to ˜1.25 mg/L, indicating that chlorates could be formed (FIG. 48). Some negative effects on plant growth were experienced at 4.55 and 6.82 mA/cm.sup.2 (FIG. 47A). In the presence of fertilizer in solution the formation of chlorates may be prevented.

Degradation of Agrichemicals by Various Water Treatment Methods

[0342] The commercialized product Roundup™ was added to deionized water at a concentration of 7 mg/L for the main active compound glyphosate. The solution was treated with varying contact times by all treatment methods previously mentioned. Both electrochemical systems used a current density of 2.27 mA/cm.sup.2 with various contact times, while the ozone and AOP treatments had an injection of ozone for 10 mins reaching 4.7±0.26 mg/L O.sub.3(aq). The AOP treatment followed the ozone treatment by passing the solution through UV light with a flow rate of 310 mL/min. There were no significant differences in the number of plants, fronds, or dry weights of Lemna minor following the AOP treatment (FIGS. 49A & 49B). However, with the BDD electrodes, there were significant increases in the number of fronds and dry weight of plants past the contact time of 2 minutes. No significant differences were found in the number of plants with any contact time that was subjected to the solution (FIG. 49A). With the DSA electrodes, there were no significant differences found in the growth of Lemna minor with a contact time of 1-minute. However, when increasing the contact time≥2 minutes, there were decreases in the growth and reproduction of plants. Ozonation had the same concentration of 4.7 mg/L used for the AOP treatment and it showed significant decreases in plant growth for all measured parameters with a contact time of 10 minutes.

[0343] All of the treatments were successful at removing glyphosate to concentrations low enough to maintain healthy plants following treatment, except for ozonation (FIG. 12). The decreases in plant growth should not be associated with the presence of glyphosate in solution but rather an ozone residual that is too high for plant growth. This occurred nevertheless with allowing the solution to stand for 20 minutes before adding the Hoagland solution and Lemna minor into Erlenmeyer flasks. A partial amount of ozone would have been consumed with the introduction of the Hoagland solution however, the residual ozone concentration must have been above 1.5 mg/L. When AOP was employed, the residual concentration of ozone was absent in solution which lead to no adverse effects on plant growth as experienced with ozone. BDD electrodes were also successful at removing glyphosate and even had significant increases in plant growth with the contact time. Without being bound by any theory, the phosphatic group and nitrogen found in glyphosate after the compound is mineralized by hydroxyl radicals and other side reactions is released. This releases orthophosphate, ammonium, and nitrate in solution and increases the amount of available nutrients needed for plant growth. This increase in nutrients leads to improved growth conditions in comparison to control plants. With the DSA electrodes, no significant differences in plant growth were observed by treating the solution with 2.27 mA/cm.sup.2 for a 1-minute contact time. Thus, indicating that glyphosate had been removed to concentrations lower than 2.5 mg/L (FIGS. 4 & 12). Increasing the contact time (>2 minutes) lead to a decrease in growth due to the residual free chlorine concentration approaching phytotoxicity for plants. The residual free chlorine concentrations at the 2-minute contact time were more than 1.5 mg/L and this shows phytotoxicity effects on Lemna minor at these higher concentrations.

[0344] Paclobutrazol was added in solution in the form of the commercialized product Bonzi™ at a concentration of 3 mg/L of paclobutrazol (FIG. 50A/50B). The solutions were then subjected to treatment by AOP, BDD, DSA and ozonation, same as the previous experiment conducted with Glyfos™. For all treatments, there were significant decreases in plant health and reproduction with all contact times that were tested. With the DSA electrodes, it showed to have an additive effect for decreasing plant health with a longer contact time of 6 minutes. No signs of improvement for Lemna minor were found with all tested parameters for this experiment.

[0345] When 3 mg/L of paclobutrazol is in solution from the commercial product Bonzi™, all treatments did not completely remove the compound. Some of the paclobutrazol and surfactants were removed by the treatments, as partially indicated by FIG. 46B. However, all treatment methods were not able to reduce the concentration lower than the LOEC levels of 0.01 mg/L previously determined by the results collected in FIGS. 43A/43B. Paclobutrazol has been shown to be highly recalcitrant, thus either one or more repetition of the treatment could be effected or stronger treatment method could be employed to completely remove the chemical. The BDD electrodes had been shown to be the most effective treatment known for removing the compound (FIGS. 46A/46B).

Recirculation Experiments with Paclobutrazol

[0346] The experiment with paclobutrazol from FIG. 50A/50B was re-performed with longer contact times by recirculating the solution through the electrochemical flow cell with BDD electrodes (FIG. 51A/51B). The solution was recirculated at a flow rate of 64 mL/min with a total volume of 2.14 L in a 3 L beaker. The solution had a contact time of 6 minutes with the electrodes and took approximately 35 minutes for the solution to recirculate completely for 1 full pass. Each pass added 6 minutes, as the solution would be in contact with the electrodes for a total of 18 minutes with a total of 3 passes. With each pass there was a positive improvement with all parameters monitored for plant health. However, there were still significant differences with even the longest contact time of 18 minutes in comparison to the control without paclobutrazol present. The solution was recirculated with longer contact times and using the same current density for identifying whether the compound can be removed effectively with BDD electrodes. Although there was still a difference in comparison to the control, there is a positive trend for remediating water quality for plant growth and function. These results suggest that a contact time of 24 minutes may remove paclobutrazol to levels low enough to have no significant differences. Upon looking at the growth parameters of plants, there is a definite indication that paclobutrazol levels were lower than 0.05 mg/L by comparing the results between FIGS. 43A/43B & 51A/51B. Furthermore, having a concentration of 3 mg/L of paclobutrazol in the source water of a greenhouse may be unlikely. Thus, the system does demonstrate that significant improvements are made to source water if paclobutrazol was only present in trace amounts.

Lemna Experiments (with Fertilizer Present):

[0347] The experiments described herein are repeated in the presence of fertilizer in solution (0.5 g/L of 20-8-20 plant prod fertilizer or half strength Hoagland solution).

TABLE-US-00003 TABLE 2 List Of Registered Pesticides (Chemical Name) CAS Registry Number (or EDF Substance ID) .ALPHA.-L-XYLO-2-HEXULOFURANOSONIC ACID, 2,3:4,6-BIS-O-(1- 52508-35-7 METHYLETHYLIDENE)-, SODIUM SALT .BETA.-D-ALLOFURANURONIC ACID, 5-[[2-AMINO-5-O-(AMINOCARBONYL)-2- 146659-78-1 DEOXY-L-XYLONOYL]AMINO]-1-(5-CARBOXY-3,4-DIHYDRO-2,4-DI . . . ABAMECTIN 71751-41-2 ABSOLUE ORANGE FLOWER 8008-57-9 AC 263222 (CADRE HERBICIDE) 81334-60-3 ACACIA MOLLISSIMA TANNIN 1401-55-4 ACEITE DE LINAZA 8001-26-1 ACEITE DE PINO 8002-09-3 ACEPHATE 30560-19-1 ACETALDEHYDE, (3,3-DIMETHYLCYCLOHEXYLIDENE)-, (E)- 26532-25-2 ACETALDEHYDE, (3,3-DIMETHYLCYCLOHEXYLIDENE)-, (Z)- 26532-24-1 ACETAMIDE, N-[2,4-DIMETHYL-5- 53780-34-0 [[(TRIFLUOROMETHYL)SULFONYL]AMINO]PHENYL]- ACETAMIDE, N-[2,4-DIMETHYL-5- 83601-83-6 [[(TRIFLUOROMETHYL)SULFONYL]AMINO]PHENYL]-, MONOPOTASSIUM SALT ACETAMINOPHEN 103-90-2 ACETIC ACID 64-19-7 ACETIC ACID, (2,4,5-TRICHLOROPHENOXY)-, 1-METHYLETHYL ESTER 93-78-7 ACETIC ACID, (2,4,5-TRICHLOROPHENOXY)-, 2-BUTOXYETHYL ESTER 2545-59-7 ACETIC ACID, (2,4,5-TRICHLOROPHENOXY)-, 2-ETHYL-4-METHYLPENTYL ESTER 69462-12-0 ACETIC ACID, (2,4,5-TRICHLOROPHENOXY)-, 2-ETHYLHEXYL ESTER 1928-47-8 ACETIC ACID, (2,4,5-TRICHLOROPHENOXY)-, COMPD. WITH 2- 53404-86-7 (DIETHYLAMINO)ETHANOL (1:1) ACETIC ACID, (2,4,5-TRICHLOROPHENOXY)-, PENTYL ESTER 120-39-8 ACETIC ACID, (2,4-DICHLOROPHENOXY)-, 2-METHYLPROPYL ESTER 1713-15-1 ACETIC ACID, (2,4-DICHLOROPHENOXY)-, AMMONIUM SALT 2307-55-3 ACETIC ACID, (2,4-DICHLOROPHENOXY)-, COMPD. WITH 1,1′,1″-NITRILOTRIS(2- 32341-80-3 PROPANOL) (1:1) ACETIC ACID, (2,4-DICHLOROPHENOXY)-, COMPD. WITH 1,1′,1″-NITRILOTRIS[2- 18584-79-7 PROPANOL] (1:1) ACETIC ACID, (2,4-DICHLOROPHENOXY)-, COMPD. WITH 1-DODECANAMINE (1:1) 2212-54-6 ACETIC ACID, (2,4-DICHLOROPHENOXY)-, COMPD. WITH 1-TETRADECANAMINE 28685-18-9 (1:1) ACETIC ACID, (2,4-DICHLOROPHENOXY)-, COMPD. WITH 2,2′,2″- 2569-01-9 NITRILOTRIS[ETHANOL] (1:1) ACETIC ACID, (2,4-DICHLOROPHENOXY)-, COMPD. WITH 2,2′-IMINOBIS[ETHANOL] 5742-19-8 (1:1) ACETIC ACID, (2,4-DICHLOROPHENOXY)-, COMPD. WITH 2-AMINOETHANOL (1:1) 3599-58-4 ACETIC ACID, (2,4-DICHLOROPHENOXY)-, COMPD. WITH 2-PROPANAMINE (1:1) 5742-17-6 ACETIC ACID, (2,4-DICHLOROPHENOXY)-, COMPD. WITH N,N- 2646-78-8 DIETHYLETHANAMINE (1:1) ACETIC ACID, (2,4-DICHLOROPHENOXY)-, COMPD. WITH N-ETHYLETHANAMINE 20940-37-8 (1:1) ACETIC ACID, (2,4-DICHLOROPHENOXY)-, COMPD. WITH N- 2008-39-1 METHYLMETHANAMINE (1:1) ACETIC ACID, (2,4-DICHLOROPHENOXY)-, LITHIUM SALT 3766-27-6 ACETIC ACID, (2,4-DICHLOROPHENOXY)-, POTASSIUM SALT 14214-89-2 ACETIC ACID, (4-CHLORO-2-METHYLPHENOXY)-, COMPD. WITH N- 2039-46-5 METHYLMETHANAMINE (1:1) ACETIC ACID, (4-CHLORO-2-METHYLPHENOXY)-, ISOOCTYL ESTER 26544-20-7 ACETIC ACID, BROMO-, 2-BUTENE-1,4-DIYL ESTER 20679-58-7 ACETIC ACID, NITRILOTRI-, TRISODIUM SALT 5064-31-3 ACETIC ACID, SODIUM SALT (2:1) 126-96-5 ACETIC ACID, TRICHLORO-, SODIUM SALT 650-51-1 ACETIC ACID, [(3,5,6-TRICHLORO-2-PYRIDINYL)OXY]-, 2-BUTOXYETHYL ESTER 64700-56-7 ACETOCHLOR 34256-82-1 ACETONE 67-64-1 ACETYLSALICYLIC ACID 50-78-2 ACIBENZOLAR-S-METHYL 135158-54-2 ACID BLUE 9,DIAMMONIUM SALT 2650-18-2 ACIDULATED COCONUT SOAPSTOCK 8001-31-8 ACIDULATED SOYBEAN SOAPSTOCK 8001-22-7 ACIFLUORFEN, SODIUM SALT 62476-59-9 ACROLEIN 107-02-8 ACRYLONITRILE 107-13-1 ACTOCOL 51-530 25322-69-4 ADEPS LANE 8006-54-0 1,1′-AETHYLEN-2,2′-BIPYRIDINIUM-DIBROMID 85-00-7 AKYPOSAL ALS 33 2235-54-3 AKYPOSAL TLS 139-96-8 ALACHLOR 15972-60-8 ALCOHOLS, C11-15, ETHOXYLATED, COMPDS. WITH IODINE 68439-47-4 ALCOHOLS, C11-15-SECONDARY, ETHOXYLATED 68131-40-8 ALCOHOLS, C8-10 85566-12-7 ALDICARB 116-06-3 ALDRIN 309-00-2 ALKENES, C14-16 ALPHA-, SULFONATED, SODIUM SALTS 68439-57-6 ALKYL DIMETHYLBENZYL AMMONIUM CHLORIDE 8001-54-5 ALKYL PYRIDINES 68391-11-7 ALKYL(C12-16)DIMETHYLBENZYLAMMONIUM CHLORIDE 68424-85-1 ALLETHRIN 584-79-2 ALLYL ALCOHOL 107-18-6 ALLYL ISOTHIOCYANATE 57-06-7 1-ALLYL-4-METHOXYBENZENE 140-67-0 ALMOND ARTIFICIAL ESSENTIAL OIL 100-52-7 ALPHA,ALPHA′-((9-OCTADECENYLIMINO)DI-2,1-ETHANEDIYL)BIS(OMEGA-HYD- 26635-93-8 ROXYPOLY(OXY-1,2-ETHANEDIYL)-, (Z)- ALPHA,ALPHA,ALPHA-TRIFLUORO-3′-ISOPROPOXY-O-TOLUANILIDE 66332-96-5 ALPHA-METOLACHLOR 87392-12-9 ALUMINUM 7429-90-5 ALUMINUM CHLORIDE 7446-70-0 ALUMINUM PHOSPHIDE 20859-73-8 ALUMINUM SULFATE 10043-01-3 AMETRYN 834-12-8 AMIDES, C12-18, N,N-BIS(HYDROXYETHYL) 68155-06-6 AMIDES, COCO, N-(2-HYDROXYETHYL)- 68140-00-1 AMIDES, SOYA, N,N-BIS(HYDROXYETHYL) 68425-47-8 AMINES, COCO ALKYL, ACETATES 61790-57-6 AMINES, COCO ALKYL, HYDROCHLORIDES 91745-52-7 AMINES, N-C12-18-ALKYLTRIMETHYLENEDI- 68155-37-3 AMINES, N-COCO ALKYLTRIMETHYLENEDI- 61791-63-7 AMINES, N-COCO ALKYLTRIMETHYLENEDI-, ACETATES 61791-64-8 AMINES, N-COCO ALKYLTRIMETHYLENEDI-, ADIPATES 68155-42-0 AMINES, N-COCO ALKYLTRIMETHYLENEDI-, GLYCOLATES 68155-43-1 AMINES, TALL-OIL ALKYL, (2,4-DICHLOROPHENOXY)ACETATES 137335-70-7 2-AMINO-4-(HYDROXYMETHYLPHOSPHINYL)BUTANOIC ACID MONOAMMONIUM 77182-82-2 SALT 4-AMINO-BENZOLSULFONYL-METHYLCARBAMAT 3337-71-1 AMINOCARB 2032-59-9 2-AMINOETHANOL 141-43-5 AMITRAZ 33089-61-1 AMITROLE 61-82-5 AMMATE 7773-06-0 AMMONIA 7664-41-7 AMMONIUM CARBONATE 506-87-6 AMMONIUM HYDROXIDE 1336-21-6 AMMONIUM OLEATE 544-60-5 AMMONIUM SILICOFLUORIDE 16919-19-0 AMMONIUM SULFATE 7783-20-2 AMMONIUM THIOSULFATE 7783-18-8 AMYL ACETATE 628-63-7 ANCYMIDOL 12771-68-5 ANHIDRIDO BUTIRICO 106-31-0 ANILAZINE 101-05-3 9,10-ANTHRACENEDIONE 84-65-1 ANTIMONY POTASSIUM TARTRATE 28300-74-5 ANTIMYCIN A 1397-94-0 ANTU 86-88-4 APPLE ACID 6915-15-7 ARAMITE 140-57-8 ARIEN 64742-16-1 AROMATIC NAPHTHA, TYPE I 64742-95-6 AROMATIC PETROLEUM DERIVATIVE SOLVENT 68477-31-6 ARQUAD 2C 61789-77-3 ARSENIC ACID 7778-39-4 ARSENIC ACID (H3ASO4), MONOAMMONIUM SALT 13462-93-6 ARSENIC AS ELEMENTAL, PRESENT AS DODECYL AND OCTYL AMMONIUM 6379-37-9 METHYL ARSENATES ARSENIC OXIDE (3) 1327-53-3 ARSENIC PENTOXIDE 1303-28-2 ARSONIC ACID, METHYL-, CALCIUM SALT (2:1) 5902-95-4 ASBESTOS (FRIABLE) 1332-21-4 ASPHALT (PETROLEUM) FUMES 8052-42-4 ASPON (NPD) 3244-90-4 ATRAZINE 1912-24-9 AURAMINE 492-80-8 AZACOSTEROL 1249-84-9 AZADIRACHTIN 11141-17-6 AZINPHOS-ETHYL 2642-71-9 AZINPHOS-METHYL 86-50-0 AZODRIN 6923-22-4 AZOXYSTROBIN 131860-33-8 BACILLUS THURINGIENSIS (BERLINER) 68038-71-1 BARBAN 101-27-9 BARIUM CARBONATE 513-77-9 BARIUM METABORATE 13701-59-2 BASIC COPPER SULFATE 1344-73-6 BASIC VIOLET 3 548-62-9 BENDIOCARB 22781-23-3 BENFLURALIN 1861-40-1 BENOMYL 17804-35-2 BENSULFURON METHYL 83055-99-6 BENSULIDE 741-58-2 BENZADOX 5251-79-6 BENZAMIDE, 5-BROMO-N-(4-BROMOPHENYL)-2-HYDROXY- 87-12-7 BENZAMIDE, N-[[[3,5-DICHLORO-4-(1,1,2,2-TETRAFLUOROETHOXY) 86479-06-3 PHENYL]AMINO]CARBONYL]-2,6-DIFLUORO- BENZENE 71-43-2 BENZENE, (2-BROMO-2-NITROETHENYL)- 7166-19-0 BENZENE, 1,2,4-TRIMETHOXY- 135-77-3 BENZENE, 1-[(DIIODOMETHYL)SULFONYL]-4-METHYL- 20018-09-1 1,2-BENZENEDICARBOXALDEHYDE 643-79-8 BENZENEDIMETHANAMINIUM, AR-DODECYL-AR,N,N,N,N′,N′,N′-HEPTAMETHYL-, 1399-80-0 DICHLORIDE, MIXT. WITH AR-DODECYL-AR,N,N,N- TETRAMETHYLBENZENEMETHANAMINIU BENZENEMETHANAMINIUM, AR-DODECYL-N,N,N-TRIMETHYL-, CHLORIDE 1330-85-4 BENZENEMETHANAMINIUM, N,N-DIMETHYL-N-TETRADECYL-, CHLORIDE 139-08-2 BENZENEMETHANAMINIUM, N,N-DIMETHYL-N-[2-[2-[METHYL-4-(1,1,3,3- 25155-18-4 TETRAMETHYLBUTYL)PHENOXY]ETHOXY]ETHYL]-, CHLORIDE BENZENEMETHANAMINIUM, N-[2-[(2,6-DIMETHYLPHENYL)AMINO]-2- 90823-38-4 OXOETHYL]-N,N-DIETHYL-, SALT WITH 1,2-BENZISOTHIAZOL-3(2H)-ONE 1,1- DIOXIDE (1:1) BENZENEMETHANOL, 4-CHLORO-.ALPHA.-(4-CHLOROPHENYL)-.ALPHA.-METHYL- 80-06-8 BENZENESULFONIC ACID, DECYL(SULFOPHENOXY)-, DISODIUM SALT 36445-71-3 BENZENESULFONIC ACID, DIMETHYL-, SODIUM SALT 1300-72-7 BENZENESULFONIC ACID, DODECYL-, POTASSIUM SALT 27177-77-1 BENZENESULFONIC ACID, METHYL-, SODIUM SALT 12068-03-0 BENZETHONIUM CHLORIDE 121-54-0 BENZINE 8032-32-4 1,2-BENZISOTHIAZOLIN-3-ONE 2634-33-5 BENZOCAINE 94-09-7 BENZOIC ACID 65-85-0 BENZOIC ACID, 2,3,6-TRICHLORO- 50-31-7 BENZOIC ACID, 3,6-DICHLORO-2-METHOXY-, COMPD. WITH 2,2′- 25059-78-3 IMINOBIS[ETHANOL] (1:1) BENZOIC ACID, 3,6-DICHLORO-2-METHOXY-, COMPD. WITH 2-(2- 104040-79-1 AMINOETHOXY)ETHANOL (1:1) BENZOIC ACID, 3,6-DICHLORO-2-METHOXY-, COMPD. WITH 2-AMINOETHANOL 53404-28-7 (1:1) BENZOIC ACID, 3,6-DICHLORO-2-METHOXY-, COMPD. WITH 2-PROPANAMINE (1:1) 55871-02-8 BENZOIC ACID, 3,6-DICHLORO-2-METHOXY-, POTASSIUM SALT 10007-85-9 BENZOIC ACID, PHENYLMETHYL ESTER 120-51-4 1,4-BENZOQUINONE, 2,3,5,6-TETRACHLORO- 118-75-2 2,2′-BENZOTHIAZYL DISULFIDE 120-78-5 BENZYL ALCOHOL 100-51-6 BENZYL BROMOACETATE 5437-45-6 BENZYLADENINE 1214-39-7 BICYCLO(2.2.1)HEPTAN-2-OL, 1,7,7-TRIMETHYL-, ACETATE, EXO- 125-12-2 BIDRIN 141-66-2 BIFENAZATE 149877-41-8 BIFENOX 42576-02-3 BIFENTHRIN 82657-04-3 BIOBAN-C 4075-81-4 BIOBAN-S 137-40-6 BIORESMETHRIN 28434-01-7 BIPHENYL 92-52-4 [1,1′-BIPHENYL]-2-OL, AMMONIUM SALT 52704-98-0 [1,1′-BIPHENYL]-2-OL, POTASSIUM SALT 13707-65-8 2,3,4,5-BIS (2-BUTENYLENE) TETRAHYDROFURFURAL 126-15-8 2,6-BIS(1-METHYLETHYL)NAPHTHALENE 24157-81-1 1,4-BIS(2-ETHYLHEXYL) SODIUM SULFOSUCCINATE 577-11-7 BIS(2-HYDROXYETHYL)LAURAMIDE 120-40-1 BIS(HYDROGENATED TALLOW ALKYL)DIMETHYLAMMONIUM BENTONITE 68953-58-2 10,10′-BIS(PHENOXYARSINYL) OXIDE 58-36-6 BIS(TRIBUTYLTIN) OXIDE 56-35-9 BIS(TRICHLORMETHYL) SULFONE 3064-70-8 BISODIUM SULFATE 7757-82-6 BISPYRIBAC-SODIUM 125401-92-5 BK2-W 9004-70-0 BL 2142 31512-74-0 BONE OIL 8001-85-2 BORATES,TETRA,SODIUM SALTS 1303-96-4 BORIC ACID 10043-35-3 BORON SODIUM OXIDE (B4NA2O7), PENTAHYDRATE 12179-04-3 BORON SODIUM OXIDE (B8NA2O13) 12008-41-2 BORON SODIUM OXIDE (B8NA2O13), TETRAHYDRATE 12280-03-4 BORON ZINC OXIDE (B6ZN2O11), HYDRATE 12447-61-9 BRILLIANT BLUE FCF 3844-45-9 BRODIFACOUM 56073-10-0 BROMACIL 314-40-9 BROMACIL LITHIUM SALT (2,4(H,3H)-PYRIMIDINEDIONE, ETHYL-3 (1- 53404-19-6 METHYLPROPYL), LITHIUM SALT) BROMADIOLONE 28772-56-7 BROMETHALIN 63333-35-7 BROMINE 7726-95-6 BROMINE CHLORIDE 13863-41-7 1-BROMO-1-(BROMOMETHYL)-1,3-PROPANEDICARBONITRILE 35691-65-7 4-BROMO-2,5-DICHLOROPHENYL DIMETHYL PHOSPHOROTHIONATE 2104-96-3 2-BROMO-2-NITROPROPANE-1,3-DIOL 52-51-7 BROMOXYNIL 1689-84-5 BROMOXYNIL OCTANOATE 1689-99-2 BROMUCONAZOLE 116255-48-2 BTC 1100 53516-75-9 BTC 776 53516-76-0 BTC 927 8045-22-5 BUFA-4,20,22-TRIENOLIDE, 6-(ACETYLOXY)-3-(.BETA.-D-GLUCOPYRANOSYLOXY)- 507-60-8 8,14-DIHYDROXY-, (3.BETA.,6.BETA.)- BUFENCARB (RE-5353) 2282-34-0 BUPROFEZIN (APPLAUD) 69327-76-0 BUSAN 1104 85264-33-1 BUSAN 74 (HPMTS) 29803-57-4 1,3-BUTANDIOL 107-88-0 BUTANEDIOIC ACID, CADMIUM SALT (1:1) 141-00-4 BUTANEDIOIC ACID, SULFO-, 1,4-DIOCTYL ESTER, SODIUM SALT 1639-66-3 1-BUTANETHIOL 109-79-5 BUTANOIC ACID, 4-(2,4-DICHLOROPHENOXY)-, COMPD. WITH N- 2758-42-1 METHYLMETHANAMINE (1:1) BUTANOIC ACID, 4-(2,4-DICHLOROPHENOXY)-, ISOOCTYL ESTER 1320-15-6 BUTANOIC ACID, 4-(2,4-DICHLOROPHENOXY)-, SODIUM SALT 10433-59-7 BUTANOIC ACID, 4-(4-CHLORO-2-METHYLPHENOXY)-, SODIUM SALT 6062-26-6 3-BUTEN-2-ONE, 4-(2,6,6-TRIMETHYL-2-CYCLOHEXEN-1-YL)-, (E)- 127-41-3 3-BUTENOIC ACID, 2-AMINO-4-(2-AMINOETHOχΥ)-, MONOHYDROCHLORIDE, [S- 55720-26-8 (E)]- BUTONATE 126-22-7 BUTOXYCARBOXIM 34681-23-7 BUTRALIN 33629-47-9 BUTYLATE 2008-41-5 C.I. BASIC GREEN 4 569-64-2 (C10-C16) ALKYLBENZENESULFONIC ACID 68584-22-5 (C10-C16)ALKYLDIMETHYLAMINE OXIDE 70592-80-2 (C12-C18) ALKYLDIMETHYLBENZYL AMMONIUM CHLORIDE 68391-01-5 (C14-C18) DIALKYLDIMETHYLAMMONIUM CHLORIDE 68002-59-5 (C6-C12) ALKYL ALCOHOL 68603-15-6 (C6-C12) ALKYLCARBOXYLIC ACID METHYL ESTER 67762-39-4 (C8-C18 AND C18)UNSATURATED ALKYL CARBOXYLIC ACID, POTASSIUM SALT 67701-09-1 (C8-C18) AND (C18) UNSATURATED ALKYLCARBOXYLIC ACID SODIUM SALT 67701-10-4 CACODYLIC ACID 75-60-5 CADMIUM CARBONATE 513-78-0 CADMIUM CHLORIDE 10108-64-2 CADRE 104098-49-9 CALCIUM ARSENATE [2ASH3O4.2CA] 7778-44-1 CALCIUM CARBONATE 471-34-1 CALCIUM CHLORIDE (CACL2) 10043-52-4 CALCIUM CYANAMIDE 156-62-7 CALCIUM CYANIDE 592-01-8 CALCIUM HYDROXIDE 1305-62-0 CALCIUM HYPOCHLORITE 7778-54-3 CALCIUM OXIDE 1305-78-8 CALCIUM OXYTETRACYCLINE 7179-50-2 CALCIUM SILICATE 10101-39-0 CALCIUM SILICATE 1344-95-2 CALCIUM SULFATE 7778-18-9 CALCIUM SULFIDE (CA(SX)) 1344-81-6 CALCIUM THIOSULFATE 10124-41-1 CAMPHECHLOR 8001-35-2 CAMPHOR 76-22-2 CAPRIC ACID 334-48-5 CAPRYLIC ACID 124-07-2 CAPSAICIN 404-86-4 CAPTAN 133-06-2 CARBAMIC ACID, 1H-BENZIMIDAZOL-2-YL, 2-(ETHOXYETHOXY)ETHYL ESTER 62732-91-6 CARBAMIC ACID, 1H-BENZIMIDAZOL-2-YL-, METHYL ESTER, PHOSPHATE (1:1) 52316-55-9 CARBAMIC ACID, [(4-AMINOPHENYL)SULFONYL]-, METHYL ESTER, 2302-17-2 MONOSODIUM SALT CARBARYL 63-25-2 CARBENDAZIM 10605-21-7 CARBOFURAN 1563-66-2 CARBON 7440-44-0 CARBON DIOXIDE 124-38-9 CARBON DISULFIDE 75-15-0 CARBON TETRACHLORIDE 56-23-5 CARBONIC ACID, AMMONIUM COPPER SALT 33113-08-5 CARBONIC ACID, COPPER(2+) SALT (1:1) 1184-64-1 CARBOPHENOTHION 786-19-6 CARBOXIN 5234-68-4 (((CARBOXYMETHYL)IMINO)BIS(ETHYLENENITRILO))TETRAACETIC ACID, 140-01-2 PENTASODIUM SALT CARFENTRAZONE-ETHYL 128639-02-1 CASTOR OIL 8001-79-4 CAUSTIC SODA 1310-73-2 CEDARWOOD OIL 8000-27-9 CETYLDIMETHYLETHYLAMMONIUM BROMIDE 124-03-8 CHEMICAL OIL (COAL) 65996-82-9 CHINOMETHIONAT (6-METHYL-1,3-DITHIOLO[4,5-B]QUINOX 2439-01-2 CHITIN 1398-61-4 CHITOSAN 9012-76-4 4-CHLOR-M-CRESOL 59-50-7 CHLORBROMURON (MALORAN) 13360-45-7 CHLORDANE 57-74-9 CHLORDIMEFORM 6164-98-3 CHLORETHOXYFOS (FORTRESS) 54593-83-8 CHLORFENAC (+SALTS) 85-34-7 CHLORFENAPYR (PIRATE) 122453-73-0 CHLORFENVINFOS 470-90-6 CHLORFLURECOL METHYL ESTER 2536-31-4 CHLORHYDRIN 96-24-2 CHLORIDAZON 1698-60-8 CHLORIMURON ETHYL 90982-32-4 CHLORINATED TRISODIUM PHOSPHATE 56802-99-4 CHLORINE 7782-50-5 CHLORINE DIOXIDE 10049-04-4 CHLORMEQUAT CHLORIDE 999-81-5 4-CHLORO-2-CYCLOPENTYLPHENOL 13347-42-7 (+-)-2-(4-CHLORO-2-METHYLPHENOXY)PROPIONIC ACID 7085-19-0 1-CHLORO-2-NITROPROPANE 2425-66-3 4-CHLORO-3,5-XYLENOL 88-04-0 2-CHLORO-N,N-DI-2-PROPENYLACETAMIDE 93-71-0 (4-CHLORO-O-TOLYLOXY)BUTYRIC ACID 94-81-5 3-CHLORO-P-TOLUIDINE 7745-89-3 1-(3-CHLOROALLYL)-3,5,7-TRIAZA-1-AZONIAADAMANTANE CHLORIDE 4080-31-3 CHLOROBENZENE 108-90-7 CHLOROBENZILATE 510-15-6 1-(2-(2-CHLOROETHOXY)PHENYLSULFONYL)-3-(4-METHOXY-6-METHYL-1,3,5-- 82097-50-5 TRIAZIN-2-YL)UREA (IUPAC) CHLOROFORM 67-66-3 CHLORONEB 2675-77-6 CHLOROPHACINONE 3691-35-8 2-CHLOROPHENOL 95-57-8 (4-CHLOROPHENOXY)ACETIC ACID 122-88-3 CHLOROPICRIN 76-06-2 CHLOROPROPHAM 101-21-3 CHLOROPROPYLATE 5836-10-2 CHLOROTHALONIL 1897-45-6 CHLOROXURON 1982-47-4 CHLORPYRIFOS 2921-88-2 CHLORPYRIFOS METHYL 5598-13-0 CHLORSULFURON 64902-72-3 CHOLECALCIFEROL 67-97-0 CHROMIC ACID 7738-94-5 CHROMIC ACID (H2CR2O7), DISODIUM SALT, DIHYDRATE 7789-12-0 CHROMIUM TRIOXIDE 1333-82-0 CITRIC ACID 77-92-9 CLETHODIM (SELECT HERBACIDE) 99129-21-2 CLODINAFOP-PROPARGYL 105512-06-9 CLOFENTEZINE 74115-24-5 CLOMAZONE (DIMETHAZONE) 81777-89-1 CLONITRALID 1420-04-8 CLOPROP (+SALTS) (FRUITONE) 53404-22-1 CLOPYRALID (LONTREL) 1702-17-6 CLORANSULAM-METHL (XDE-565) 147150-35-4 COAL TARS 8007-45-2 COBALT NAPHTHENATE 61789-51-3 (COCO ALKYL)DIETHANOLAMIDES 68603-42-9 COCOA FATTY ACIDS, POTASSIUM SALTS 61789-30-8 COCONUT FATTY ACID, SODIUM SALT 61789-31-9 COMPOUND 105 137-16-6 COPPER 7440-50-8 COPPER (11)-8- HYDROXYQUINOLINE 10380-28-6 COPPER (I) CHLORIDE 7758-89-6 COPPER ARSENATE 10103-61-4 COPPER CARBONATE (BASIC) 12069-69-1 COPPER CHLORIDE HYDROXIDE (CU2CL(OH)3) 1332-65-6 COPPER CHLORIDE HYDROXIDE (CU2CL(OH)3), MIXT. WITH COPPER HYDROXIDE 8012-69-9 SULFATE (CU4(OH)6(SO4)) COPPER CHLORIDE OXIDE, HYDRATE 1332-40-7 COPPER NAPHTHENATE 1338-02-9 COPPER OXIDE 1317-38-0 COPPER ZINC HYDROXIDE SULFATE 55072-57-6 COPPER(2), TETRAAMINE- 16828-95-8 COPPER, BIS(2-AMINOETHANOLATO-N,O)- 14215-52-2 COPPER, BIS(D-GLUCONATO-O1,O2)- 527-09-3 COPPER, [[2,2′,2″-NITRILOTRIS[ETHANOLATO]](2-)-N,O,O′,O″]- 82027-59-6 COTTON OIL 8001-29-4 COUMAFURYL (FUMARIN) 117-52-2 COUMAPHOS 56-72-4 CREOSOTES 8001-58-9 CRESOL (MIXED ISOMERS) 1319-77-3 CROTOXYPHOS 7700-17-6 CRUDE LIGHT OIL (COAL) 65996-78-3 CRUFOMATE 299-86-5 CRYOLITE 15096-52-3 CUPRIC (II) OXALATE 814-91-5 CUPRIC ACETOARSENITE 12002-03-8 CUPRIC HYDROXIDE 20427-59-2 CUPRIC NITRATE 3251-23-8 CUPRIC SULFATE 7758-98-7 CUPRIETHYLENE-DIAMINE SOLUTION 13426-91-0 CUPROUS OXIDE 1317-39-1 CUPROUS THIOCYANATE 1111-67-7 CYANAMIDE 420-04-2 CYANAZINE 21725-46-2 CYANURIC ACID 108-80-5 CYCLANILIDE 113136-77-9 CYCLOATE 1134-23-2 CYCLOBUTANEETHANOL, 1-METHYL-2-(1-METHYLETHENYL)-, (1R-CIS)- 26532-22-9 CYCLOHEXANE 110-82-7 CYCLOHEXANOL, 5-METHYL-2-(1-METHYLETHYL)- 1490-04-6 CYCLOHEXANONE 108-94-1 CYCLOHEXIMIDE 66-81-9 CYCLOPROPANECARBOXYLIC ACID, 2,2-DIMETHYL-3-(2-METHYL-1-PROPENYL)-, 42534-61-2 2-METHYL-4-OXO-3-(2-PROPENYL)-2-CYCLOPENTEN-1-YL ESTER, [1.ALPHA.(S*),3. CYCLOPROPANECARBOXYLIC ACID, 2,2-DIMETHYL-3-(2-METHYL-1-PROPENYL)-, 28434-00-6 2-METHYL-4-OXO-3-(2-PROPENYL)-2-CYCLOPENTEN-1-YL ESTER, [1R-[1.ALPHA.(S* CYCLOPROPANECARBOXYLIC ACID, 2,2-DIMETHYL-3-(2-METHYL-1-PROPENYL)-, 39515-40-7 CYANO(3-PHENOXYPHENYL)METHYL ESTER CYFLUTHRIN 68359-37-5 CYHALOFOP BUTYL 122008-85-9 CYHALOTHRIN K 91465-08-6 CYMOXANIL 57966-95-7 CYPERMETHRIN 52315-07-8 CYPRAZINE 22936-86-3 CYPROCONAZOLE (SAN 619F) 94361-06-5 CYPRODINIL 121552-61-2 CYROMAZINE 66215-27-8 2,4-D 94-75-7 2,4-D 2-ETHYL-4-METHYLPENTYL ESTER 53404-37-8 2,4-D 2-ETHYLHEXYL ESTER 1928-43-4 2,4-D BUTOXYETHYL ESTER 1929-73-3 2,4-D BUTYL ESTER 94-80-4 2,4-D PROPYLENE GLYCOL BUTYL ETHER ESTER 1320-18-9 2,4-D SODIUM SALT 2702-72-9 2,4-D, ISOOCTYL ESTER 25168-26-7 2,4-D, ISOPROPYL ESTER 94-11-1 D-STREPTAMINE, O-2-DEOXY-2-(METHYLAMINO)-.ALPHA.-L- 298-39-5 GLUCOPYRANOSYL-(1.FWDARW.2)-O-5-DEOXY-3-C-FORMYL-.ALPHA.-L- LYXOFURANOSYL-(1.FWDARW.4)-N D-TRANS-ALLETHRIN 28057-48-9 DAMINOZIDE 1596-84-5 DASANIT 115-90-2 DAZOMET 533-74-4 2,4-DB 94-82-6 DDT 50-29-3 1-DECANAMINIUM, N,N-DIMETHYL-N-OCTYL-, CHLORIDE 32426-11-2 1-DECANAMINIUM, N-DECYL-N-METHYL-N-[3-(TRIMETHOXYSILYL)PROPYL]-, 68959-20-6 CHLORIDE 1-DECANAMINIUM, N-ISONONYL-N,N-DIMETHYL-, CHLORIDE 138698-36-9 DECANEDIOIC ACID, CADMIUM SALT (1:1) 4476-04-4 1-DECANOL 112-30-1 5-DECEN-1-OL, (E)- 56578-18-8 5-DECEN-1-OL, ACETATE, (E)- 38421-90-8 DEET 134-62-3 DEHYDROABIETYLAMINE ACETATE 2026-24-6 DEHYDROABIETYLAMINE ETHYLENE OXIDE 51344-62-8 DELTAMETHRIN (DECA-) 52918-63-5 DEMETON 8065-48-3 DENATONIUM BENZOATE 3734-33-6 DEODORIZER DISTILLATE 68476-80-2 DESMEDIPHAM 13684-56-5 DEXTRIN 9004-53-9 2,6-DI-TERT-BUTYL-P-CRESOL 128-37-0 DIACETONE ALCOHOL 123-42-2 DIALLATE 2303-16-4 DIAMMONIUM EDTA 20824-56-0 DIAZINON 333-41-5 DIBENZOTHIAZINE 92-84-2 1,2-DIBROMO-3-CHLOROPROPANE (DBCP) 96-12-8 2,2-DIBROMO-3-NITRILOPROPIONAMIDE 10222-01-2 1,2-DIBROMOETHANE 106-93-4 3,5-DIBROMOSALICYLANILIDE 2577-72-2 DIBUTYL PHTHALATE 84-74-2 DICAMBA 1918-00-9 DICHLOBENIL 1194-65-6 DICHLOFENTHION 97-17-6 DICHLONE 117-80-6 2,2-DICHLOROPROPIONIC ACID 75-99-0 DICHLORAN 99-30-9 DICHLORFLURECOL-METHYL 21634-96-8 3,6-DICHLORO-2-PYRIDINECARBOXYLIC ACID, MONOETHANOLAMINE SALT 57754-85-5 1,3-DICHLORO-5,5-DIMETHYL-HYDANTOIN 118-52-5 DICHLOROBENZALKONIUM CHLORIDE 8023-53-8 1,2-DICHLOROBENZENE 95-50-1 1,4-DICHLOROBENZENE 106-46-7 (3,4-DICHLOROBENZYL)DODECYLDIMETHYLAMMONIUM CHLORIDE 102-30-7 DICHLORODIFLUOROMETHANE 75-71-8 1,2-DICHLOROETHANE 107-06-2 DICHLOROISOCYANURIC ACID 2782-57-2 DICHLOROMETHANE 75-09-2 DICHLOROPHENE 97-23-4 1,2-DICHLOROPROPANE 78-87-5 2,3-DICHLOROPROPENE 78-88-6 1,3-DICHLOROPROPENE (MIXED ISOMERS) 542-75-6 DICHLORVOS 62-73-7 DICLOFOP METHYL 51338-27-3 DICLOSULAM 145701-21-9 DICOFOL 115-32-2 DIDECYLDIMETHYLAMMONIUM CHLORIDE 7173-51-5 DIELDRIN 60-57-1 DIENOCHLOR 2227-17-0 DIETHATYL ETHYL 38727-55-8 DIETHYLENE GLYCOL MONOMETHYL ETHER 111-77-3 DIFENOCONAZOLE (DIVIDEND) 119446-68-3 DIFETHIALONE 104653-34-1 DIFLUBENZURON 35367-38-5 DIFLUFENZOPYR 109293-97-2 DIFLUFENZOPYR-SODIUM 109293-98-3 1,2-DIHYDRO-2,2,4-TRIMETHYL-6-ETHOXYQUINOLINE 91-53-2 (+-)-2-(4,5-DIHYDRO-4-METHYL-4(1-METHYLETHYL)-5-OXO-1H-IMIDAZOL-2-YL)- 81335-77-5 5-ETHYL-3-PYRIDINECARBOXYLIC ACID 2-(4,5-DIHYDRO-4-METHYL-4-(1-METHYLETHYL)-5-OXO-1H-IMIDAZOL-2-YL)- -3- 81335-37-7 QUINOLINECARBOXYLIC ACID 2,2′-DIHYDROXY-3,3′-DIMETHYL-5,5′-DICHLORODIPHENYL SULFIDE 4418-66-0 DIISOBUTYL KETONE;2,6-DIMETHYL-4-HEPTONE 108-83-8 DIMETHAMETRYN 22936-75-0 DIMETHENAMID (SAN 582H) 87674-68-8 DIMETHIPIN 55290-64-7 DIMETHOATE 60-51-5 DIMETHOMORPH 110488-70-5 DIMETHOXANE 828-00-2 2,6-DIMETHOXY-N-(3-(1-ETHYL-1-METHYLPROPYL)-5-ISOXAZOLYL)BENZAMID- E 82558-50-7 DIMETHRIN 70-38-2 DIMETHYL PHTHALATE 131-11-3 DIMETHYL TETRACHLOROTEREPHTHALATE 1861-32-1 2,6-DIMETHYL-2-OCTEN-8-OL 106-22-9 1,2-DIMETHYL-3,5-DIPHENYL-1-H-PYRAZOLIUM METHYL SULFATE 43222-48-6 DIMETHYLAMINE DICAMBA 2300-66-5 1,1-DIMETHYLETHYL HYDROPEROXIDE 75-91-2 DIMETHYLNAPHTHALENE 28804-88-8 DIMETHYLOXAZOLIDINE, 4,4- 51200-87-4 2,4-DIMETHYLPHENOL 105-67-9 DIMETILAN 644-64-4 DINITRAMINE 29091-05-2 1,3-DINITRO-4-CHLOROBENZENE 97-00-7 2,6-DINITRO-N,N-DIPROPYL-4-ISOPROPYLANILINE 33820-53-0 4,6-DINITRO-O-CRESOL 534-52-1 DINITROBUTYL PHENOL 88-85-7 2,4-DINITROPHENOL 51-28-5 DINOCAP 39300-45-3 DINOSEB, AMMONIUM SALT 6365-83-9 1,3,2-DIOXABORINANE, 2,2′-OXYBIS[4,4,6-TRIMETHYL- 14697-50-8 1,3,2-DIOXABORINANE, 2,2′-[(1-METHYL-1,3-PROPANEDIYL)BIS(OXY)]BIS[4- 2665-13-6 METHYL- DIPENTENE 138-86-3 DIPHACINONE 82-66-6 DIPHENAMID 957-51-7 DIPHENYLAMINE 122-39-4 DIPHENYLSTIBINE 2-ETHYLHEXOATE 5035-58-5 DIPOTASSIUM ENDOTHALL 2164-07-0 DIPROPETRYN 4147-51-7 DIPROPYL ISOCINCHOMERONATE 136-45-8 DIPROPYLENE GLYCOL 25265-71-8 DIPROPYLENE GLYCOL MONOMETHYL ETHER 34590-94-8 DISODIUM CYANODITHIOIMIDOCARBONATE 138-93-2 DISODIUM METHANEARSONATE 144-21-8 DISODIUM PHOSPHATE 7558-79-4 DISTILLATES (PETROLEUM), HYDROTREATED (MILD) HEAVY PARAFFINIC (9C1) 64742-54-7 DISTILLATES (PETROLEUM), HYDROTREATED (MILD) LIGHT PARAFFINIC (9C1) 64742-55-8 DISTILLATES (PETROLEUM), SOLVENT-REFINED (MILD) HEAVY PARAFFINIC (9C1) 64741-88-4 DISTILLATES (PETROLEUM), SOLVENT-REFINED (MILD) LIGHT NAPHTHENIC (9C1) 64741-97-5 DISTILLATES (PETROLEUM), SOLVENT-REFINED (MILD) LIGHT PARAFFINIC (9C1) 64741-89-5 DISTILLATES, PETROLEUM, C12-30-AROM. 68602-80-2 DISTILLATES, WOOD TAR 91995-59-4 DISULFOTON 298-04-4 DITALIMFOS 5131-24-8 DITHIANON 3347-22-6 DITHIOPYR (MON 7200) 97886-45-8 DIURON 330-54-1 DMPA (ZYTRON) 299-85-4 8,10-DODECADIEN-1-OL, (E,E)- 33956-49-9 2,4-DODECADIENOIC ACID, 11-METHOXY-3,7,11-TRIMETHYL-, 1-METHYLETHYL 65733-16-6 ESTER, [S-(E,E)]- 2,4-DODECADIENOIC ACID, 3,7,11-TRIMETHYL-, 2-PROPYNYL ESTER,[S-(E,E)]- 65733-20-2 2,4-DODECADIENOIC ACID, 3,7,11-TRIMETHYL-, ETHYL ESTER, [S-(E,E)]- 65733-18-8 1-DODECANAMINIUM, N,N,N-TRIMETHYL-, CHLORIDE 112-00-5 1-DODECANAMINIUM, N,N-DIMETHYL-N-OCTYL-, CHLORIDE 10361-16-7 DODECANOIC ACID, POTASSIUM SALT 10124-65-9 1-DODECANOL 112-53-8 2,6,10-DODECATRIEN-1-OL, 3,7,11-TRIMETHYL- 4602-84-0 1,6,10-DODECATRIEN-3-OL, 3,7,11-TRIMETHYL- 7212-44-4 8-DODECEN-1-OL, (Z)- 40642-40-8 DODECYL GUANIDINE HYDROCHLORIDE 13590-97-1 DODECYLBENZENESULFONIC ACID 27176-87-0 DODINE 2439-10-3 2,4-DP 120-36-5 DPX-M 6316 79277-27-3 (E)-3,7-DIMETHYL-2,6-OCTADIEN-1-OL 106-24-1 (E,E)-2,4-HEXADIENOIC ACID 110-44-1 E-8-DODECENYL ACETATE 38363-29-0 EDETATE SODIUM 64-02-8 EDETATE TRISODIUM 150-38-9 EMAMECTIN 137512-74-4 ENDOSULFAN 115-29-7 ENDOTHALL 145-73-3 ENDRIN 72-20-8 ENQUIK 21351-39-3 EPICHLOROHYDRIN 106-89-8 EPN 2104-64-5 ERBON 136-25-4 ESFENVALERATE 66230-04-4 ETHALFLURALIN 55283-68-6 ETHAMETSULFURON 97780-06-8 ETHANAMINE, 2-DECYLTHIO-, HYDROCHLORIDE 36362-09-1 ETHANOL 64-17-5 ETHANOL, 2-(3,3-DIMETHYLCYCLOHEXYLIDENE)-, (Z)- 26532-23-0 ETHANOL, 2-(HYDROXYMETHYLAMINO)- 34375-28-5 ETHEPHON 16672-87-0 ETHIOLATE 2941-55-1 ETHION 563-12-2 ETHOFENPROX (ETOFENPROX) 80844-07-1 ETHOFUMESATE 26225-79-6 ETHOPROP 13194-48-4 ETHYL ACETATE 141-78-6 ETHYL DIPROPYLTHIOCARBAMATE 759-94-4 ETHYL FORMATE 109-94-4 ETHYLENE 74-85-1 ETHYLENE GLYCOL 107-21-1 ETHYLENE GLYCOL MONOBUTYL ETHER 111-76-2 ETHYLENE GLYCOL MONOMETHYL ETHER 109-86-4 ETHYLENE OXIDE 75-21-8 ETHYLENE THIOUREA 96-45-7 ETHYLENEDIAMINE 107-15-3 ETHYLENEDIAMINE TETRAACETIC ACID (EDTA) 60-00-4 ETHYLENEDIAMINETETRAACETIC ACID, TRIPOTASSIUM SALT 17572-97-3 (ETHYLENEDINITRILO)-TETRAACETIC ACID DISODIUM SALT 139-33-3 EUGENOL 97-53-0 FAMPHUR 52-85-7 FENAMINOSULF (DIAZOBEN) 140-56-7 FENAMIPHOS 22224-92-6 FENARIMOL 60168-88-9 FENBUCONAZOLE (FENETHANIL) 114369-43-6 FENBUTATIN OXIDE 13356-08-6 FENHEXAMID 126833-17-8 FENITROTHION 122-14-5 FENOXAPROP ETHYL(2-(4-((6-CHLORO-2- 66441-23-4 BENZOXAZOLYEN)OXY)PENOXY)PROPANIC ACID, ETHYL ESTER) FENOXYCARB 72490-01-8 FENPROPATHRIN 39515-41-8 FENPRYROXIMATE 134098-61-6 FENRIDAZON 83588-43-6 FENTHION 55-38-9 FENTICHLOR 97-24-5 FENURON-TCA 4482-55-7 FENVALERATE 51630-58-1 FERBAM 14484-64-1 FERRIC SULFATE 10028-22-5 FERROUS AMMONIUM SULFATE 10045-89-3 FIPRONIL 120068-37-3 FLUAZIFOP-BUTYL 69806-50-4 FLUAZINAM 79622-59-6 FLUCARBAZONE SODIUM 181274-17-9 FLUCHLORALIN 33245-39-5 FLUCYTHRINATE 70124-77-5 FLUDIOXONIL (MAXIM) 131341-86-1 FLUMETRALIN 62924-70-3 FLUMETSULAM (XRD-498) 98967-40-9 FLUMICLORAC PENTYL 87546-18-7 FLUMIOXAZIN 103361-09-7 FLUOMETURON 2164-17-2 FLUOROACETAMIDE 640-19-7 FLUOROACETIC ACID, SODIUM SALT 62-74-8 FLUORODIFEN 15457-05-3 FLUROXYPYR 1-METHYLHEPTYL ESTER 81406-37-3 FLUTHIACET-METHYL (ACTION) 117337-19-6 FLUVALINATE 69409-94-5 FLUVALINATE, TAU- 102851-06-9 FOLPET 133-07-3 FOMESAFEN 72178-02-0 FOMESAFEN SODIUM (FLEX) 108731-70-0 FONOFOS 944-22-9 FORAMSULFURON 173159-57-4 FORMALDEHYDE 50-00-0 FORMETANATE HYDROCHLORIDE 23422-53-9 FORMIC ACID 64-18-6 FOSAMINE AMMONIUM 25954-13-6 FOSETYL AL 39148-24-8 FOSTHIAZATE 98886-44-3 FOSTHIETAN 21548-32-3 FUMARIC ACID 110-17-8 GAMMA-LINDANE 58-89-9 GASOLINE 8006-61-9 GIBB-3-ENE-1,10-DICARBOXYLIC ACID, 2,4A,7-TRIHYDROXY-1-METHYL-8- 125-67-7 METHYLENE-, 1,4A-LACTONE, MONOPOTASSIUM SALT, (1.ALPHA.,2.BETA.,4A.ALPHA.,4B GIBB-3-ENE-1,10-DICARBOXYLIC ACID, 2,4A-DIHYDROXY-1-METHYL-8- 8030-53-3 METHYLENE-1,4A-LACTONE MIXT. WITH GIBBANE-1,10-DICARBOXYLIC ACID, 2,4A-DIHYDRO GIBBERELLIC ACID 77-06-5 GLUTARALDHYDE 111-30-8 GLYCERIN MIST 56-81-5 GLYCINE, N,N′-1,2-ETHANEDIYLBIS[N-(CARBOXYMETHYL)-, TETRAPOTASSIUM 5964-35-2 SALT GLYCINE, N-(HYDROXYMETHYL)-, MONOSODIUM SALT 70161-44-3 GLYCINE, N-(PHOSPHINOMETHYL)-, AMMONIUM SALT 114370-14-8 GLYCINE, N-(PHOSPHONOMETHYL)-, COMPD. WITH 2-PROPANAMINE (1:1) 38641-94-0 GLYCINE, N-(PHOSPHONOMETHYL)-, SODIUM SALT (2:3) 70393-85-0 GLYCOLIC ACID 79-14-1 GLYCOLS, POLYETHYLENE, MONO(HYDROGEN SULFATE), DODECYL ETHER, 9004-82-4 SODIUM SALT GLYODIN 556-22-9 GLYPHOSATE 1071-83-6 GLYPHOSATE TRIMESIUM 81591-81-3 GLYPHOSINE 2439-99-8 15H 9003-29-6 2(3H)-BENZOTHIAZOLETHIONE, SODIUM SALT 2492-26-4 2(3H)-BENZOTHIAZOLETHIONE, ZINC SALT 155-04-4 2(3H)-FURANONE, 5-(1-DECENYL)DIHYDRO-, [R-(Z)]- 64726-91-6 2(3H)-FURANONE, 5-HEPTYLDIHYDRO- 104-67-6 2(3H)-FURANONE, DIHYDRO-5-PENTYL- 104-61-0 3(2H)-ISOTHIAZOLONE, 4,5-DICHLORO-2-OCTYL- 64359-81-5 1H,3H,5H-OXAZOLO[3,4-C]OXAZOLE, 7A-ETHYLDIHYDRO- 7747-35-5 1H,3H,5H-OXAZOLO[3,4-C]OXAZOLE-7A(7H)-METHANOL 6542-37-6 1H,7H-NAPHTHO[1,8-BC:4,4A-C′]DIFURAN-5,10A(8H)-DICARBOXYLIC ACID, 10- 108189-58-8 (ACETYLOXY)-4-(HEXAHYDRO-6A-HYDROXY-7A-METHYL-2,7- METHANOFURO[2,3-B] . . . 3H-1,2-DITHIOL-3-ONE, 4,5-DICHLORO- 1192-52-5 2H-1,3-THIAZINE, TETRAHYDRO-2-(NITROMETHYLENE)- 58842-20-9 1H-2,1,3-BENZOTHIADIAZIN-4(3H)-ONE, 3-(1-METHYLETHYL)-, 2,2-DIOXIDE, 50723-80-3 SODIUM SALT 1H-INDENE-1,3(2H)-DIONE, 2-(2,2-DIMETHYL-1-OXOPROPYL)-, ION(1−), SODIUM 6120-20-3 1H-INDENE-1,3(2H)-DIONE, 2-(DIPHENYLACETYL)-, ION(1−), SODIUM 42721-99-3 1H-INDOLE 120-72-9 1H-INDOLE-3-BUTANETHIOIC ACID, S-PHENYL ESTER 85977-73-7 HAIMASED 540-72-7 HALOFENOZIDE 112226-61-6 HALOSULFURON METHYL 100784-20-1 HEAVY ALKYLATE HYDROCARBONS 68919-17-5 HEPTACHLOR 76-44-8 1-HEPTADECANECARBOXYLIC ACID 57-11-4 HEPTANOIC ACID, 2,6-DIBROMO-4-CYANOPHENYL ESTER 56634-95-8 HEXACHLOROBENZENE 118-74-1 1,2,3,4,5,6-HEXACHLOROCYCLOHEXANE (MIXTURE OF ISOMERS) 608-73-1 HEXACHLOROCYCLOPENTADIENE 77-47-4 HEXACHLOROPHENE (HCP) 70-30-4 7,11-HEXADECADIEN-1-OL, ACETATE 50933-33-0 7,11-HEXADECADIEN-1-OL, ACETATE, (E,Z)- 53042-79-8 7,11-HEXADECADIEN-1-OL, ACETATE, (Z,Z)- 52207-99-5 1-HEXADECANOL 36653-82-4 11-HEXADECENAL, (Z)- 53939-28-9 2,4-HEXADIENOIC ACID, POTASSIUM SALT, (2E,4E)- 24634-61-5 1,3-HEXANEDIOL, 2-ETHYL- 94-96-2 1-HEXANOL 111-27-3 1-HEXANOL, 2-ETHYL- 104-76-7 HEXAZINONE 51235-04-2 HEXYLENE GLYCOL 107-41-5 #2 HOME HEATING OILS 68476-30-2 HYDANTOIN, 3-BROMO-1-CHLORO-5,5-DIMETHYL- 126-06-7 HYDRAMETHYLNON 67485-29-4 HYDRIODIC ACID 10034-85-2 HYDROCARBONS 68920-06-9 HYDROCHLORIC ACID 7647-01-0 HYDROFLUORIC ACID 7664-39-3 HYDROGEN CYANIDE 74-90-8 HYDROGEN PEROXIDE (CONC > 52%) 7722-84-1 (HYDROLYSIS PRODUCTS OF SULFATED CASTOR OIL), SODIUM SALTS 68187-76-8 HYDROPRENE (ALTOZAR) 41096-46-2 1-HYDROXY-4-TERT-BUTYLBENZENE 98-54-4 4-HYDROXY-BUTYL ESTER BENZOIC ACID 94-26-8 2-HYDROXYBENZOIC ACID 69-72-7 1-(2-HYDROXYETHYL)-2-(TALL OIL ALKYL)-2-IMIDAZOLINE 61791-39-7 HYDROXYLETHYL OCTYL SULFIDE 3547-33-9 1-(HYDROXYMETHYL)-5,5-DIMETHYL HYDANTOIN 116-25-6 2-HYDROXYNAPHTHALENE 135-19-3 1-HYDROXYOCTANE 111-87-5 1-(4-HYDROXYPHENYL)-2-BROMOETHANONE 2491-38-5 1-(2-HYDRPXYETHYL)-2-HEPTADECYLIMIDAZOLINE 27136-73-8 HYMEXAZOL (TACHIGAREN) 10004-44-1 HYPOCHLORITE 7778-66-7 HYPOCHLOROUS ACID 7790-92-3 IMAZALIL 35554-44-0 IMAZAMETHABENZ 81405-85-8 IMAZAPYR (ARSENAL) 81334-34-1 IMIDACLOPRID 105827-78-9 IMIDAN 732-11-6 2,4-IMIDAZOLIDINEDIONE, 1,3-BIS(HYDROXYMETHYL)-5,5-DIMETHYL- 6440-58-0 2,4-IMIDAZOLIDINEDIONE, 1,3-DIBROMO-5,5-DIMETHYL- 77-48-5 2,4-IMIDAZOLIDINEDIONE, 1,3-DICHLORO-5-ETHYL-5-METHYL- 89415-87-2 2,4-IMIDAZOLIDINEDIONE, 1-BROMO-3-CHLORO-5,5-DIMETHYL- 16079-88-2 2,2′-IMINOBISETHANOL N-COCO ALKYL DERIVS. 61791-31-9 INDOLE-3-BUTYRIC ACID 133-32-4 INDOXACARB (DPX-MP062) 173584-44-6 IODINE 7553-56-2 3-IODO-2-PROPYNYL BUTYLCARBAMATE 55406-53-6 IPRODIONE 36734-19-7 ISOFENPHOS 25311-71-1 ISOPROPYL ACETATE 108-21-4 ISOPROPYL ALCOHOL 67-63-0 KAOLIN 1332-58-7 KBR 3023 (PROPIDINE) 119515-38-7 KEROSENE 8008-20-6 KINETIN 525-79-1 KINOXIFEN 124495-18-7 5-KLOR-2-METYL-4-ISOTIAZOLIN-3-ON OCH 2-METYL-4-ISOTIAZOLIN-3-ON (I 26172-55-4 FÖRHÅLLANDE 3:1) > 15 PPM KRESOXIM-METHYL 143390-89-0 LACTOFEN 77501-63-4 LAURYL DIMETHYL BENZYL AMMONIUM CHLORIDE 139-07-1 LEAD ACETATE 301-04-2 LEAD ARSENATE 7784-40-9 LETHANE 112-56-1 LINURON 330-55-2 LITHIUM HYPOCHLORITE 13840-33-0 LITHIUM PERFLUOROOCTANE SULFONATE 29457-72-5 LURSECT 51609-52-0 M-CRESOL 108-39-4 MAGNESIUM CHLORIDE 7786-30-3 MAGNESIUM PHOSPHIDE 12057-74-8 MAGNESIUM SULFATE 7487-88-9 MALATHION 121-75-5 MANCOZEB 8018-01-7 MANEB 12427-38-2 MANGANESEDIMETHYLDITHIOCARBAMATE 15339-36-3 MEDIUM STEAM CRACKED AROMATIC NAPHTHA (PETROLEUM) 68516-20-1 MEFENOXAM TECHNICAL 70630-17-0 MEFLUIDINE DIETHANOLAMINE 53780-36-2 1-MENTHENE-8-OL 98-55-5 MEPIQUAT CHLORIDE 24307-26-4 2-MERCAPTOBENZOTHIAZOLE 149-30-4 MERCAPTODIMETHUR 2032-65-7 MERCURY CHLORIDE (2) 7487-94-7 MERCURY(1+), [2,2′,2″-NITRILOTRIS[ETHANOL]-N,O,O′,O″]PHENYL-, SALT WITH 2- 23319-66-6 HYDROXYPROPANOIC ACID (1:1) MERCURY, (2-ETHYLHEXANOATO)PHENYL- 13302-00-6 MERCURY, (2-HYDROXYPROPANOATO)PHENYL- 122-64-5 MERCURY, (9-OCTADECENOATO-O)PHENYL-, (Z)- 104-60-9 MERCURY, (NITRATO-O)PHENYL- 55-68-5 MERCURY, DIPHENYL)[.MU.-[(TETRAPROPENYL)BUTANEDIOATO(2-)-O:O′]]DI- 27236-65-3 MERCURY, PHENYL(8-QUINOLINOLATO-N1,O8)- 14354-56-4 MERCURY, [.MU.-[ORTHOBORATO(2−)-O:O′]]DIPHENYLDI- 6273-99-0 MERPHOS 150-50-5 MESOTRIONE 104206-82-8 2-MESYL-2-METHYLPROPIONALDEHYDE O-METHYLCARBAMOYLOXIME 1646-88-4 METACETALDEHYDE 108-62-3 METALAXYL 57837-19-1 METALDEHYDE 9002-91-9 METARHIZIUM ANISOPLIAE ESF1 67892-13-1 METHAM SODIUM 137-42-8 METHAMIDOPHOS 10265-92-6 METHANESULFONIC ACID, THIO-, O-(2-HYDROXYPROPYL) ESTER 30388-01-3 METHANIMIDAMIDE, N′-(4-CHLORO-2-METHYLPHENYL)-N,N-DIMETHYL-, 19750-95-9 MONOHYDROCHLORIDE METHANOL 67-56-1 METHANOL, (1H,3H,5H-OXAZOLO[3,4-C]OXAZOL-7A(7H)-YLMETHOXY)- 59720-42-2 METHANOL, [[[1-METHYL-2-(5-METHYL-3- 97553-90-7 OXAZOLIDINYL)ETHYOXY]METHOXY]METHOXY]- METHANONE, (5-CYCLOPROPYL-4-ISOXAZOLYL)[2-(METHYLSULFONYL)-4- 141112-29-0 (TRIFLUOROMETHYL)PHENYL]- METHAZOLE 20354-26-1 METHIDATHION 950-37-8 METHOMYL 16752-77-5 METHOPRENE 40596-69-8 METHOXONE 94-74-6 METHOXONE SODIUM SALT ((4-CHLORO-2-METHYLPGENOXY) ACETATE SODIUM 3653-48-3 SALT) 1-(2-METHOXY-1-METHYLETHOXY)-2-PROPANOL 20324-32-7 1-METHOXY-4-(1-PROPENYL)BENZENE 104-46-1 2-(((((4-METHOXY-6-METHYL-1,3,5-TRIAZIN-2YL)AMINO)CARBONYL)AMINO)- 74223-64-6 SULFONYL)BENZOIC ACID METHYL ESTER 2-(METHOXYCARBONYL)ANILINE 134-20-3 4-(METHOXYCARBONYL)PHENOL 99-76-3 METHOXYCHLOR 72-43-5 METHOXYFENOZIDE 161050-58-4 METHYL BROMIDE 74-83-9 METHYL DEMETON 8022-00-2 METHYL ISOBUTYL KETONE 108-10-1 METHYL ISOTHIOCYANATE 556-61-6 METHYL NAPHTHALENE 1321-94-4 METHYL NONYL KETONE 112-12-9 METHYL PARATHION 298-00-0 2-(METHYL(1-OXO-9-OCTADECENYL)AMINO)ETHANESULFONIC ACID, SODIUM 137-20-2 SALT METHYL-2,3,5,6-TETRACHLORO-4-PYRIDYLSULPHON E 13108-52-6 2-METHYL-2-PROPENOIC ACID, DODECYL ESTER 142-90-5 1-METHYL-3-PHENYL-5-(3-(TRIFLUOROMETHYL)PHENYL)-4(1H)-PYRIDINONE 59756-60-4 METHYL-4-ISOTHIAZOLIN 2682-20-4 4-METHYLBENZENESULFONIC ACID 104-15-4 METHYLENE BLUE 61-73-4 METHYLENEBISTHIOCYANAT 6317-18-6 1-METHYLETHYL TETRADECANOATE 110-27-0 2-METHYLPROPANOIC ACID 79-31-2 METIRAM 9006-42-2 METOBROMURON 3060-89-7 METOLACHLOR 51218-45-2 METRIBUZIN 21087-64-9 METRONIDAZOLE 443-48-1 MEVINPHOS 7786-34-7 MEXACARBATE 315-18-4 MGK-264 113-48-4 MINERAL OIL SULFONIC ACIDS, SODIUM SALTS 68608-26-4 MIREX 2385-85-5 MITIN FF 3567-25-7 MOLINATE 2212-67-1 MON 21200 (GENESIS) 82697-71-0 MONURON 150-68-5 MONURON TCA (UROX) 140-41-0 MORPHOLINE 110-91-8 MORPHOLINE, 4,4′-(2-ETHYL-2-NITRO-1,3-PROPANEDIYL)BIS- 1854-23-5 MORPHOLINE, 4-(2-NITROBUTYL)- 2224-44-4 MORPHOLINE, 4-CYCLODODECYL-2,6-DIMETHYL-, ACETATE 31717-87-0 MSMA 2163-80-6 MUSCALURE 27519-02-4 MYCLOBUTANIL 88671-89-0 MYRISTYL ALCOHOL 112-72-1 N,N-DIMETHYL-N-(3-(TRIMETHOXYSILYL)PROPYL)-1-OCTADECANAMINIUM 27668-52-6 CHLORIDE N-(2-(BISCARBOXYMETHYLAMINO)ETHYL)-N-(2-HYDROXYETHYL)GLYCINE 139-89-9 TRISODIUM SALT N-ALKYL (5% C5-18, 61% C12, 23% C14, 11% C16) DIMETHYL BENZYL AMMONIUM 63449-41-2 CHLORIDE N-ALKYL DIMETHYLETHYLBENZYL AMMONIUM CHLORIDE 68956-79-6 N-METHYL NEODECANAMIDE (MNDA) 105726-67-8 N-METHYLOL CHLOROACETAMIDE 2832-19-1 N-PROPYL ALCOHOL 71-23-8 NABAM 142-59-6 NALED 300-76-5 NAPHTHALENE 91-20-3 NAPHTHALENE, 1,4-DIMETHYL- 571-58-4 1-NAPHTHALENEACETAMIDE 86-86-2 1-NAPHTHALENEACETIC ACID 86-87-3 1-NAPHTHALENEACETIC ACID, AMMONIUM SALT 25545-89-5 1-NAPHTHALENEACETIC ACID, ETHYL ESTER 2122-70-5 1-NAPHTHALENEACETIC ACID, POTASSIUM SALT 15165-79-4 1-NAPHTHALENEACETIC ACID, SODIUM SALT 61-31-4 NAPHTHO[2,3-D]-1,3-DIOXOLE-5,6-DICARBOXYLIC ACID, 5,6,7,8-TETRAHYDRO-7- 83-59-0 METHYL-, DIPROPYL ESTER 2-NAPHTHYLOXACETIC ACID 120-23-0 NAPROPAMIDE 15299-99-7 NAPTALAM (ALANAP-1) 132-66-1 NAPTALAM, SODIUM SALT 132-67-2 NATRIUMTETRABORAT ANHYDRID 1330-43-4 NEBURON 555-37-3 NEOMYCIN SULFATE 1405-10-3 NICKEL (NICKEL SULFATE HEXAHYDRATE) 10101-97-0 NICOSULFURON (ACCENT) 111991-09-4 NICOTINE AND SALTS 54-11-5 NICOTINE SULFATE 65-30-5 NITRALIN 4726-14-1 NITRAPYRIN 1929-82-4 1,1′,1″-NITRILOTRI-2-PROPANOL 122-20-3 NITROBENZENE 98-95-3 NITROFEN 1836-75-5 NITROGEN 7727-37-9 4-NITROPHENOL 100-02-7 4-NITROPHENOL SODIUM SALT 824-78-2 NONANOIC ACID, SULFOPHENYL ESTER, SODIUM SALT 91125-43-8 2-(2-(2-(2-(NONYLPHENOXY)ETHOXY)ETHOXY)ETHOXY)ETHANOL 9016-45-9 NONYLPHENOXYPOLYETHOXYETHANOL - IODINE COMPLEX 35860-86-7 NOREA (NORURON) 18530-56-8 NORFLURAZON 27314-13-2 NOVALURON 116714-46-6 O-PHENYLPHENATE, SODIUM 132-27-4 9-OCTADECEN-1-AMINIUM, N-ETHYL-N,N-DIMETHYL-, BROMIDE 6458-13-5 9-OCTADECENOIC ACID (Z)-, COMPD. WITH 2,2′,2″-NITRILOTRIS[ETHANOL](1:1) 2717-15-9 9-OCTADECENOIC ACID (Z)-, COPPER SALT (2+) 1120-44-1 9-OCTADECENOIC ACID (Z)-, SULFONATED, SODIUM SALTS 68443-05-0 1,6-OCTADIEN-3-OL, 3,7-DIMETHYL- 78-70-6 1,6-OCTADIENE, 7-METHYL-3-METHYLENE- 123-35-3 1-OCTANAMINIUM, N,N-DIMETHYL-N-OCTYL-, CHLORIDE 5538-94-3 1-OCTANECARBOXYIC ACID 112-05-0 OCTANOIC ACID, COPPER SALT 20543-04-8 1-OCTEN-3-OL 3391-86-4 OCTHILINONE 26530-20-1 OIL MIST, MINERAL 8012-95-1 OIL OF BLACK PEPPER 8006-82-4 OIL OF CITRONELLA 8000-29-1 OIL OF LEMONGRASS 8007-02-1 OILS, EUCALYPTUS 8000-48-4 OLEIC ACID 112-80-1 OLEIC ACID POTASSIUM SALT 143-18-0 ORTHO-BENZYL-P-CHLOROPHENOL 120-32-1 ORYZALIN 19044-88-3 OVEX 80-33-1 7-OXABICYCLO[2.2.1]HEPTANE-2,3-DICARBOXYLIC ACID, COMPD. WITH N,N- 66330-88-9 DIMETHYLCOCOAMINE (1:1) 7-OXABICYCLO[2.2.1]HEPTANE-2,3-DICARBOXYLIC ACID, DISODIUM SALT 129-67-9 OXADIXYL (SAN 371F) 77732-09-3 OXALIC ACID 144-62-7 OXAMYL 23135-22-0 1,4-OXATHIIN-3-CARBOXAMIDE, 5,6-DIHYDRO-2-METHYL-N-PHENYL-, 4,4- 5259-88-1 DIOXIDE OXINE BENZOATE 7091-57-8 OXIRANE, 2-DECYL-3-(5-METHYLHEXYL)-, CIS- 29804-22-6 OXIRANE, METHYL-, POLYMER WITH OXIRANE, COMPD. WITH IODINE 26617-87-8 OXIRANE, METHYL-, POLYMER WITH OXIRANE, MONOBUTYL ETHER, COMPD. 68610-00-4 WITH IODINE OXYDEMETON METHYL 301-12-2 OXYDIAZON 19666-30-9 (OXYDIETHYLENEGLYCOL)BIS(COCO ALKYL)DIMETHYL AMMONIUM CHLORIDE 68607-28-3 OXYFLUORFEN 42874-03-3 OXYTETRACYCLINE HYDROCHLORIDE (INTERNAL USE) 2058-46-0 2,3-P-DIOXANEDITHIOL S,S-BIS(O,O-DIETHYL PHOSPHORODITHIOATE) 78-34-2 2-(P-HYDROXYPHENYL)GLYOXYLOHYDROXYMOYL CHLORIDE 34911-46-1 P-TERT-AMYLPHENOL 80-46-6 P-TERT-AMYLPHENOL, POTASSIUM SALT 53404-18-5 PACLOBUTRAZOL 76738-62-0 PARABENS 94-13-3 PARAFORMALDEHYDE 30525-89-4 PARAQUAT 1910-42-5 PARAQUAT METHOSULFATE 2074-50-2 PARATHION 56-38-2 PEBULATE 1114-71-2 PENDIMETHALIN 40487-42-1 PENTACHLOROPHENOL 87-86-5 2,3,4,5,6-PENTAHYDROXYHEXANOIC ACID 526-95-4 PENTANE 109-66-0 1-PENTANETHIOL 110-66-7 PERACETIC ACID 79-21-0 PERBORIC ACID, SODIUM SALT, MONOHYDRATE 10332-33-9 PERFLUIDONE 37924-13-3 PERMETHRIN 52645-53-1 PEROXYCARBONIC ACID, TETRATHIO-, DISODIUM SALT 7345-69-9 PEROXYMONOSULFURIC ACID, MONOPOTASSIUM SALT 10058-23-8 PERTHANE 72-56-0 PETROLEUM DISTILLATES 8002-05-9 1-PHENANTHRENEMETHANAMINE, 1,2,3,4,4A,9,10,10A-OCTAHYDRO-1,4A- 1446-61-3 DIMETHYL-7- . . . PHENMEDIPHAM 13684-63-4 PHENOL 108-95-2 PHENOL, 2-(1-METHYLPROPYL)-4,6-DINITRO-, COMPD. WITH 2,2′,2″- 6420-47-9 NITRILOTRIS[ETHANOL] (1:1) PHENOL, 2-(1-METHYLPROPYL)-4,6-DINITRO-, SODIUM SALT 35040-03-0 PHENOL, 2-METHOXY-5-N1TRO-, SODIUM SALT 67233-85-6 PHENOL, 2-N1TRO-, SODIUM SALT 824-39-5 PHENOL, 3-(1-METHYLETHYL)-, METHYLCARBAMATE 64-00-6 PHENOL, 4-(1,1-DIMETHYLPROPYL)-, SODIUM SALT 31366-95-7 PHENOL, 4-CHLORO-2-(PHENYLMETHYL)-, POTASSIUM SALT 35471-49-9 PHENOL, 4-CHLORO-2-(PHENYLMETHYL)-, SODIUM SALT 3184-65-4 PHENOL, 4-NITRO-3-(TRIFLUOROMETHYL)- 88-30-2 PHENOL, METHYL-, POTASSIUM SALT 12002-51-6 PHENOTHRIN 26002-80-2 PHENTHOATE 2597-03-7 1-PHENYL-2-ETHANOL 60-12-8 PHENYLMERCURIC ACETATE 62-38-4 2-PHENYLPHENOL 90-43-7 PHEROMONE: GRAPE BERRY MOTH 16974-11-1 PHORATE 298-02-2 PHOSACETIM 4104-14-7 PHOSALONE 2310-17-0 PHOSPHAMIDON 13171-21-6 PHOSPHINE 7803-51-2 PHOSPHINIC ACID, COMPD. WITH 2-(4-THIAZOLYL)-1H-BENZIMID AZOLE (1:1) 28558-32-9 PHOSPHORIC ACID 7664-38-2 PHOSPHORIC ACID, BIS(2-ETHYLHEXYL) ESTER, COMPD. WITH 2,2′-(COCO 68649-38-7 ALKYLIMINO)BIS[ETHANOL] PHOSPHORIC ACID, DIOCTYL ESTER, COMPD. WITH 2,2′- 68961-66-0 (DODECYLIMINO)BIS(ETHANOL) (1:1) PHOSPHORIC ACID, IRON(3+) SALT (1:1) 10045-86-0 PHOSPHORIC ACID, MONO(2-ETHYLHEXYL) ESTER 1070-03-7 PHOSPHORIC ACID, MONO(2-ETHYLHEXYL)ESTER, COMPDS. WITH 120579-32-0 DIETHANOLAMINE N-COCO ALKYL DERIVS. (1:1) PHOSPHORIC ACID, MONOOCTYL ESTER, COMPD. WITH 2,2′- 125091-04-5 (DODECYLIMINO)BIS(ETHANOL) (1:1) PHOSPHOROTHIOIC ACID, O-[5-CHLORO-1-( 1-METHYLETHYL)-1H-1,2,4-TRIAZOL-3- 42509-80-8 YL] O,O-DIETHYL ESTER PHOSPHORUS (YELLOW OR WHITE) 7723-14-0 PHOSPHORUS PENTOXIDE 1314-56-3 PICLORAM 1918-02-1 PICLORAM TRIETHYLAMINE SALT 35832-11-2 PIPERALIN 3478-94-2 PIPERAZINE DIHYDROCHLORIDE 142-64-3 PIPERINE 94-62-2 PIPERONYL BUTOXIDE 51-03-6 PIRIMICARB 23103-98-2 PIRIMIFOS-ETHYL 23505-41-1 PIRIMIPHOS METHYL 29232-93-7 2-PIVALYL-1,3-INDANDIONE (PINDONE) 83-26-1 POLY(DIMETHYLDIALLYLAMMINIUM CHLORIDE) 26062-79-3 POLY(IMINOCARBONIMIDOYLIMINOCARBONIMIDOYLIMINO-1,6-HEXANEDIYL), 32289-58-0 HYDROCHLORIDE POLY(OXY-1,2-ETHANEDIYL), .ALPHA.-(NONYLPHENYL)-.OMEGA.-HYDROXY-, 11096-42-7 COMPD. WITH IODINE POLY(OXY-1,2-ETHANEDIYL), .ALPHA.-ISOOCTADECYL-.OMEGA.-HYDROXY- 52292-17-8 POLY(OXY-1,2-ETHANEDIYL), .ALPHA.-[4-(1,1,3,3-TETRAMETHYLBUTYL)PHENYL]- 53404-04-9 .OMEGA.-HYDROXY-, COMPD. WITH IODINE POLY(OXYMETHYLENE), .ALPHA.-(1H,3H,5H-OXAZOLO[3,4-C]OXAZOL-7A(7H)- 56709-13-8 YLMETHYL)-.OMEGA.-HYDROXY- POLYCHLORINATED TERPHENYLS 61788-33-8 (POLYETHYL)BENZENES 64742-94-5 POLYOXYETHYLENE (20) SORBITAN MONOLAURATE 9005-64-5 POLYVINYL PYRROLIDONE 9003-39-8 POLY[OXY(METHYL-1,2-ETHANEDIYL)], .ALPHA.-BUTYL-.OMEGA.-HYDROXY- 9003-13-8 POTASSIUM BROMIDE 7758-02-3 POTASSIUM CHROMATE 7789-00-6 POTASSIUM CYANIDE 151-50-8 POTASSIUM DICHLORO ISOCYANURATE 2244-21-5 POTASSIUM DICHROMATE 7778-50-9 POTASSIUM DIMETHYLDITHIOCARBAMATE 128-03-0 POTASSIUM HYDROXIDE 1310-58-3 POTASSIUM HYROXYMETHYL-N-METHYL-DITHIOCARBAMATE 51026-28-9 POTASSIUM IODIDE 7681-11-0 POTASSIUM IODIDE (K(13)) 12298-68-9 POTASSIUM N-METHYLDITHIOCARBAMATE 137-41-7 POTASSIUM NITRATE 7757-79-1 POTASSIUM PERMANGANATE 7722-64-7 POTASSIUM PYROPHOSPHATE 7320-34-5 POTASSIUM SALT OF ETHYLENEDIAMINETETRAACETIC ACID 7379-27-3 POTASSIUM SOAP OF TALL OIL FATTY ACIDS (C18) 61790-44-1 POTASSIUM SORBATE 590-00-1 PRALLETHRIN (ETOC) 23031-36-9 PRIMISULFURON-METHYL 86209-51-0 PRODIAMINE (RYDEX) 29091-21-2 PROFENOFOS 41198-08-7 PROFLURALIN 26399-36-0 PROHEXADIONE CALCIUM 127277-53-6 PROMETON 1610-18-0 PROMETRYN 7287-19-6 PROMEXAL (MTI) 82633-79-2 PRONAMIDE 23950-58-5 PROPACHLOR 1918-16-7 PROPAMOCARB HYDROCHLORIDE 25606-41-1 1,3-PROPANEDIOL, 2-ETHYL-2-NITRO- 597-09-1 1,2,3-PROPANETRICARBOXYLIC ACID, 2-HYDROXY-, COPPER SALT 10402-15-0 1,2,3-PROPANETRIOL TRI(12-HYDROXYSTEARATE) 8001-78-3 PROPANIL 709-98-8 PROPANOIC ACID, 2-(2,4,5-TRICHLOROPHENOXY)-, COMPD. WITH 2,2′,2″- 17369-89-0 NITRILOTRIS[ETHANOL] (1:1) PROPANOIC ACID, 2-(2,4,5-TRICHLOROPHENOXY)-, COMPD. WITH N- 55617-85-1 METHYLMETHANAMINE (1:1) PROPANOIC ACID, 2-(2,4,5-TRICHLOROPHENOXY)-, POTASSIUM SALT 2818-16-8 PROPANOIC ACID, 2-(2,4-DICHLOROPHENOXY)-, 2-BUTOXYETHYL ESTER 53404-31-2 PROPANOIC ACID, 2-(2,4-DICHLOROPHENOXY)-, COMPD. WITH N- 53404-32-3 METHYLMETHANAMINE (1:1) PROPANOIC ACID, 2-(2,4-DICHLOROPHENOXY)-, ISOOCTYL ESTER 28631-35-8 PROPANOIC ACID, 2-(4-CHLORO-2-METHYLPHENOXY)-, (R)- 16484-77-8 PROPANOIC ACID, 2-(4-CHLORO-2-METHYLPHENOXY)-, COMPD. WITH 2,2′- 1432-14-0 IMINOBIS[ETHANOL] (1:1) PROPANOIC ACID, 2-(4-CHLORO-2-METHYLPHENOXY)-, COMPD. WITH N- 32351-70-5 METHYLMETHANAMINE (1:1) PROPANOIC ACID, 2-(4-CHLORO-2-METHYLPHENOXY)-, ISOOCTYL ESTER 28473-03-2 PROPANOIC ACID, 2-(4-CHLORO-2-METHYLPHENOXY)-, POTASSIUM SALT 1929-86-8 PROPANOIC ACID, 2-HYDROXY-, (S)- 79-33-4 PROPANOIC ACID, 2-PHENYLETHYL ESTER 122-70-3 PROPANOIC ACID, 2-[4-[(6-CHLORO-2-BENZOXAZOLYL)OXY]PHENOXY]-, ETHYL 71283-80-2 ESTER, (R)- PROPANOIC ACID, 2-[4-[[5-(TRIFLUOROMETHYL)-2-PYRIDINYL]OXY]PHENOXY]-, 79241-46-6 BUTYL ESTER, (R)- 1-PROPANOL, 2-[(HYDROXYMETHYL)AMINO]-2-METHYL- 52299-20-4 2-PROPANONE, 1,1,1,3,3,3-HEXACHLORO- 116-16-5 PROPARGITE 2312-35-8 PROPAZINE 139-40-2 2-PROPEN-1-OL, 3-PHENYL- 104-54-1 2-PROPENAL, 3-PHENYL- 104-55-2 2-PROPENOIC ACID, 2-METHYL-, METHYL ESTER = STANNANE, 26354-18-7 TRIBUTYLMEACRYLATE 2-PROPENOIC ACID, 3-(4-METHOXYPHENYL)-, 2-ETHOXYETHYL ESTER 104-28-9 PROPETAMPHOS 31218-83-4 PROPHAM 122-42-9 PROPICONAZOLE 60207-90-1 PROPIONIC ACID 79-09-4 PROPOXUR 114-26-1 PROPYLENE GLYCOL 57-55-6 PROPYLENE OXIDE 75-56-9 PROSULFURON (CGA-152005) 94125-34-5 PYMETROZINE 123312-89-0 PYRACLOSTROBIN 175013-18-0 PYRETHRUM 8003-34-7 PYRIDABEN 96489-71-3 3,6-PYRIDAZINEDIONE, 1,2-DIHYDRO-, MONOPOTASSIUM SALT 28382-15-2 PYRIDINE 110-86-1 PYRIDINE, 4-AMINO- 504-24-5 3-PYRIDINECARBOXYLIC ACID, 2-[4,5-DIHYDRO-4-METHYL-4-(1-METHYLETHYL)- 81510-83-0 5-OXO-1H-IMIDAZOL-2-YL]-, COMPD. WITH 2-PROPANAMINE(1:1) 3-PYRIDINECARBOXYLIC ACID, 2-[4,5-DIHYDRO-4-METHYL-4-(1-METHYLETHYL)- 114311-32-9 5-OXO-1H-IMIDAZOL-2-YL]-5-(METHOXYMETHYL)- 3-PYRIDINECARBOXYLIC ACID, 2-[4,5-DIHYDRO-4-METHYL-4-(1-METHYLETHYL)- 101917-66-2 5-OXO-1H-IMIDAZOL-2-YL]-5-ETHYL-, MONOAMMONIUM SALT 2-PYRIDINECARBOXYLIC ACID, 4-AMINO-3,5,6-TRICHLORO-, COMPD.WITH 1,1′,1″- 6753-47-5 NITRILOTRIS[2-PROPANOL] (1:1) 2-PYRIDINECARBOXYLIC ACID, 4-AMINO-3,5,6-TRICHLORO-, ISOOCTYL ESTER 26952-20-5 2-PYRIDINECARBOXYLIC ACID, 4-AMINO-3,5,6-TRICHLORO-, MONOPOTASSIUM 2545-60-0 SALT PYRITHIOBAC-SODIUM 123343-16-8 2-PYRROLIDINONE, 1-ETHENYL-, HOMOPOLYMER, COMPD. WITH IODINE 25655-41-8 QUATERNARY AMMONIUM COMPOUNDS, BENZYL-C10-18- 91721-81-2 ALKYLBIS(HYDROXYETHYL), CHLORIDES QUATERNARY AMMONIUM COMPOUNDS, BENZYL-C12-18-ALKYLDIMETHYL, 68989-01-5 SALTS WITH 1,2-BENZISOTHIAZOL-3(2H)-ONE 1,1-DIOXIDE (1:1) QUATERNARY AMMONIUM COMPOUNDS, BENZYLCOCO ALKYLDIMETHYL, 61789-71-7 CHLORIDES QUATERNARY AMMONIUM COMPOUNDS, BENZYLDI-C12-18-ALKYLMETHYL, 73049-75-9 CHLORIDES QUATERNARY AMMONIUM COMPOUNDS, C12-14- 85409-23-0 ALKYL[(ETHYLPHENYL)METHYL]DIMETHYL, CHLORIDES QUATERNARY AMMONIUM COMPOUNDS, C12-16- 68989-02-6 ALKYL[(DICHLOROPHENYL)METHYL]DIMETHYL, CHLORIDES QUATERNARY AMMONIUM COMPOUNDS, C12-18- 8045-21-4 ALKYLDIMETHYLETHYLBENZYL, CHLORIDES QUATERNARY AMMONIUM COMPOUNDS, C14-18-ALKYLETHYLDIMETHYL 134595-54-3 QUATERNARY AMMONIUM COMPOUNDS, C14-18-ALKYLTRIMETHYL, BROMIDES 68424-92-0 QUATERNARY AMMONIUM COMPOUNDS, C14-18-ALKYLTRIMETHYL, CHLORIDES 68002-63-1 QUATERNARY AMMONIUM COMPOUNDS, C16-18-ALKYLTRIMETHYL, CHLORIDES 68002-62-0 QUATERNARY AMMONIUM COMPOUNDS, DI-C8-18-ALKYLDIMETHYL, 73398-64-8 CHLORIDES QUINCLORAC (FACET) 84087-01-4 3-QUINOLINECARBOXYLIC ACID, 2-[4,5-DIHYDRO-4-METHYL-4-(1- 81335-47-9 METHYLETHYL)-5-OXO-1H-IMIDAZOL-2-YL]-, MONOAMMONIUM SALT 3-QUINOLINECARBOXYLIC ACID, 2-[4,5-DIHYDRO-4-METHYL-4-(1- 81335-46-8 METHYLETHYL)-5-OXO-1H-IMIDAZOL-2-YL]-, SODIUM SALT QUINONE 106-51-4 QUINTOZENE 82-68-8 QUIZALOFOP P-ETHYL 100646-51-3 QUIZALOFOP-ETHYL 76578-14-8 RESIN ACIDS AND ROSIN ACIDS, COPPER SALTS 9007-39-0 RESMETHRIN 10453-86-8 RIMSULFURON (DPX-E9636) 122931-48-0 RONNEL 299-84-3 ROTENONE, COMMERCIAL 83-79-4 (RS)-2-(3,5-DICHLOROPHENYL)-2-(2,2,2-TRICHLOROETHYL)OXIRANE 58138-08-2 (RS)-2-METHYL-1-PYRIMIDIN-5-YL-1-(4-TRIFLUOROMETHOXY)PHENYLPROPAN- - 56425-91-3 2-OL (RS)-SEC-BUTYLAMINE 13952-84-6 (4RS,5RS)-5-(4-CHLOROPHENYL)-N-CYCLOHEXYL-4-METHYL-2-OXO-1,3-THIA- 78587-05-0 ZOLIDINE-3-CARBOXAMIDE RYANODINE 15662-33-6 (S)-ALPHA-CYANO-3-PHENOXYBENZYL (1R)-CIS-2,2-DIMETHYL-3-((RS)-1,2,2,2- 66841-25-6 TETRABROMOETHYL)-CYCLOPROPA- NECARBOXYLATE S,S,S-TRIBUTYLTRITHIOPHOSPHATE 78-48-8 SABADILLA 8051-02-3 SEC-BUTYL ALCOHOL 78-92-2 SESONE 136-78-7 SETHOXYDIM 74051-80-2 SIDURON 1982-49-6 SILICA GEL 63231-67-4 SILICA, AMORPHOUS 61790-53-2 SILICA, AMORPHOUS HYDRATED 7631-86-9 SILICIC ACID (H2S1O3), DISODIUM SALT 6834-92-0 SILVER 7440-22-4 SILVER NITRATE 7761-88-8 SILVER OXIDE (AG4O4) 155645-89-9 SIMAZINE 122-34-9 SODIUM 4,6-DINITRO-O-CRESOL 2312-76-7 SODIUM ALKYL ARYL SULFONATE 68411-30-3 SODIUM ARSENATE 13464-38-5 SODIUM ARSENITE 7784-46-5 SODIUM AZIDE 26628-22-8 SODIUM BENZOATE 532-32-1 SODIUM BICARBONATE 144-55-8 SODIUM BICHROMATE 10588-01-9 SODIUM BISULFATE 7681-38-1 SODIUM BISULFITE 7631-90-5 SODIUM BROMIDE 7647-15-6 SODIUM CACODYLATE 124-65-2 SODIUM CARBONATE 497-19-8 SODIUM CHLORATE 7775-09-9 SODIUM CHLORIDE 7647-14-5 SODIUM CHLORITE 7758-19-2 SODIUM CHROMATE 7775-11-3 SODIUM CYANIDE 143-33-9 SODIUM DEHYDROACETATE 4418-26-2 SODIUM DICAMBA 1982-69-0 SODIUM DICHLORO-S-TRIAZINETRIONE 2893-78-9 SODIUM DIMETHYLDITHIOCARBAMATE 128-04-1 SODIUM DODECYLBENZENE SULFONATE 25155-30-0 SODIUM FLUORIDE 7681-49-4 SODIUM FLUOSILICATE 16893-85-9 SODIUM HEXAMETAPHOSPATE 10124-56-8 SODIUM HYDROSULFIDE 16721-80-5 SODIUM HYPOCHLORITE 7681-52-9 SODIUM LAURYL SULFATE 151-21-3 SODIUM METABISULFITE 7681-57-4 SODIUM METABORATE 7775-19-1 SODIUM NITRATE 7631-99-4 SODIUM NITRITE 7632-00-0 SODIUM OMADINE 15922-78-8 SODIUM PENTACHLOROPHENATE 131-52-2 SODIUM PERCARBONATE 15630-89-4 SODIUM PHENATE 139-02-6 SODIUM PHOSPHATE, MONOBASIC 7558-80-7 SODIUM PHOSPHATE, TRIBASIC 7601-54-9 SODIUM SESQUICARBONATE 533-96-0 SODIUM SILICATE 1344-09-8 SODIUM SULFIDE (NA2S) 1313-82-2 SODIUM TRIPOLYPHOSPHATE 7758-29-4 SODIUM-2-PYRIDINETHIOL-1-OXIDE 3811-73-2 SODIUM-P-TOLUENESULPHONCHLORAMIDE 127-65-1 SOLVENT NAPHTHA (PETROLEUM), LIGHT ALIPHATIC 64742-89-8 SOLVENT NAPHTHA (PETROLEUM), MEDIUM ALIPHATIC 64742-88-7 SPIRO[11-OXABICYCLO[8.1.0]UNDEC-6-ENE-2,2′-OXIRAN]-3-ONE, 8-METHYLENE-5- 61228-92-0 (1-METHYLETHYL)-, [1R-(1R*,2R*,5S*,6E,10R*)]- SQUALANE 111-01-3 STANNANE, (ACETYLOXY)TRIBUTYL- 56-36-0 STANNANE, TRIBUTYL[(1-OXO-2-PROPENYL)OXY]- 13331-52-7 STANNANE, TRIBUTYL[(1-OXO-9,12-OCTADECAD 24124-25-2 STANNANE, TRIBUTYL[(1-OXONEODECYL)OXY]- 28801-69-6 STANNANE, TRIBUTYL[[2-[(TRIBUTYLSTANNYL)OXY]BENZOYL]OXY]- 22330-14-9 STANNANE, TRIBUTYL[[[1,2,3,4,4A,4B,5,6,1 26239-64-5 STIROFOS 22248-79-9 STODDARD SOLVENT 8052-41-3 STREPTOMYCIN 57-92-1 STREPTOMYCIN SULFATE 3810-74-0 STRYCHNINE 57-24-9 STRYCHNINE, SULFATE 60-41-3 SUCROSE 57-50-1 SULFACETAMIDE 144-80-9 SULFALLATE 95-06-7 SULFAMIC ACID 5329-14-6 SULFAQUINOXALINE 59-40-5 SULFENTRAZONE 122836-35-5 SULFLURAMID 4151-50-2 SULFOMETURON METHYL 74222-97-2 SULFONAMIDE 63-74-1 1-(4-SULFOPHENYL)-4-((4-SULFOPHENYL)AZO)-1H-PYRAZOLE-3-CARBOXYLIC 1934-21-0 SULFOSULFURON [MON 31500] 141776-32-1 SULFOTEP 3689-24-5 SULFOXIDE 120-62-7 SULFUR 7704-34-9 SULFUR DIOXIDE 7446-09-5 SULFURIC ACID 7664-93-9 SULFURIC ACID, COPPER(2+) SALT (1:1), PENTAHYDRATE 7758-99-8 SULFURIC ACID, IRON(2+) SALT (1:1), HEPTAHYDRATE 7782-63-0 SULFURIC ACID, IRON(2+) SALT (1:1), MONOHYDRATE 17375-41-6 SULFURIC ACID, ZINC SALT (1:1), MONOHYDRATE 7446-19-7 SULFURYL FLUORIDE 2699-79-8 SULPROFOS 35400-43-2 SUMILARV (PYRIPROXYFEN) 95737-68-1 2,4,5-T 93-76-5 2,4,5-T COMPOUND WITH N-METHYLMETHANAMINE (1:1) 6369-97-7 2,4,5-T ESTERS 93-79-8 2,4,5-T TRIETHYLAMINE SALT 2008-46-0 TAR ACIDS, COAL, CRUDE 65996-85-2 TCMTB 21564-17-0 TEBUCONAZOLE (FOLICUR) 107534-96-3 TEBUFENOZIDE 112410-23-8 TEBUPIRIMFOS 96182-53-5 TEBUTHIURON 34014-18-1 TECNAZENE 117-18-0 TEFLUTHRIN 79538-32-2 TEMEPHOS 3383-96-8 TEPP 107-49-3 TEPRALOXYDIM 149979-41-9 TERBACIL 5902-51-2 TERBUFOS 13071-79-9 TERRAZOLE 2593-15-9 TERT-BUTYL ALCOHOL 75-65-0 2,4,11,13-TETRAAZATETRADECANEDIIMIDAMIDE, N,N″-BIS(4-CHLOROPHENYL)- 56-95-1 3,12-DIIMINO-, DIACETATE TETRACAINE HYROCHLORIDE 136-47-0 1,1,2,2-TETRACHLOROETHANE 79-34-5 TETRACHLOROETHYLENE 127-18-4 2,3,4,6-TETRACHLOROPHENOL,POTASSIUM SALT 53535-27-6 2,3,4,6-TETRACHLOROPHENOL,SODIUM SALT 25567-55-9 TETRACHLOROPHENOLS 25167-83-3 TETRACHLORVINPHOS 961-11-5 1-TETRADECANAMINIUM, N-ETHYL-N,N-DIMETHYL-, BROMIDE 68527-84-4 11-TETRADECEN-1-OL, (E)- 35153-18-5 11-TETRADECEN-1-OL, ACETATE, (E)- 33189-72-9 11-TETRADECEN-1-OL, ACETATE, (Z)- 20711-10-8 TETRADIFON 116-29-0 TETRAGLYCINE HYDROPERIODIDE 7097-60-1 1,2,3,6-TETRAHYDRO-3,6-DIOXOPYRIDAZINE 123-33-1 1,2,3,4-TETRAHYDRONAPHTHALENE 119-64-2 TETRAIODOETHYLENE 513-92-8 TETRAMETHRIN 7696-12-0 (1,1,3,3-TETRAMETHYLBUTYL)PHENOL 27193-28-8 TETRASODIUM PYROPHOSPHATE 7722-88-5 TETRASUL 2227-13-6 THIABENDAZOLE 148-79-8 THIAFLUAMIDE (FOE 5043) 142459-58-3 THIAMETHOXAM 153719-23-4 THIAZOPYR (MON 13200) 117718-60-2 THIDIAZURON 51707-55-2 THIOBENCARB 28249-77-6 2,2′-THIOBIS(4,6-DICHLORO)PHENOL 97-18-7 1,1′-THIOBISETHANE 352-93-2 THIODICARB 59669-26-0 THIOPHANATE ETHYL 23564-06-9 THIOPHANATE-METHYL 23564-05-8 THIRAM 137-26-8 THPS 55566-30-8 THYMOL 89-83-8 TOLUENE 108-88-3 TORAK 10311-84-9 2,4,5-TP ACID (SILVEX) 93-72-1 TRALKOXYDIM 87820-88-0 1-TRIACONTANOL 593-50-0 TRIADIMEFON 43121-43-3 TRIADIMENOL (BAYTAN) 55219-65-3 TRIALLATE 2303-17-5 3,5,7-TRLAZA-1-AZONIATRICYCLO[3.3.1.1(3,7)]DECANE, 1-METHYL-, CHLORIDE 76902-90-4 3,5,7-TRIAZATRICYCLO[3.1.1.1(3,7)]DECANE, 1-(3-CHLORO-2-PROPENYL)-, 51229-78-8 CHLORIDE, (Z)- 1,3,5-TRIAZINE-1,3,5(2H,4H,6H)-TRIETHANOL (9CI) 4719-04-4 1,3,5-TRIAZINE-2,4,6(1H,3H,5H)-TRIONE, 1,3-DICHLORO-, SODIUMSALT, 51580-86-0 DIHYDRATE 1,3,5-TRIAZINE-2,4,6-TRIAMINE, N,N′,N′′-TRICHLORO- 7673-09-8 1,3,5-TRIAZINE-2,4-DIAMINE, 6-CHLORO-N-(1,1-DIMETHYLETHYL)-N′-ETHYL- 5915-41-3 1,3,5-TRIAZINE-2,4-DIAMINE, N-(1,1-DIMETHYLETHYL)-N′-ETHYL-6- 886-50-0 (METHYLTHIO)- 1,3,5-TRIAZINE-2,4-DIAMINE, N-CYCLOPROPYL-N′-(1,1-DIMETHYLETHYL)-6- 28159-98-0 (METHYLTHIO)- TRIBENURON METHYL 101200-48-0 3,4,5-TRIBRMOSALICYLANILIDE 87-10-5 TRIBUTYLTIN BENZOATE 4342-36-3 TRIBUTYLTIN CHLORIDE 1461-22-9 TRIBUTYLTIN FLUORIDE 1983-10-4 TRIBUTYLTIN METHACRYLATE 2155-70-6 TRICHLORFON 52-68-6 1,3,5-TRICHLORO-1,3,5-TRIAZINE-2,4,6 (1H,3H,5H)-TRIONE 87-90-1 TRICHLOROACETIC ACID 76-03-9 1,2,4-TRICHLOROBENZENE 120-82-1 TRICHLOROBENZYL CHLORIDE 1344-32-7 1,1,1-TRICHLOROETHANE 71-55-6 TRICHLOROETHYLENE 79-01-6 TRICHLOROFLUOROMETHANE 75-69-4 2,4,5-TRICHLOROPHENOL 95-95-4 2,4,6-TRICHLOROPHENOL 88-06-2 TRICLOCARBAN 101-20-2 TRICLOPYR (SALTS & ESTERS) 55335-06-3 TRICLOPYR TRIETHYLAMMONIUM SALT 57213-69-1 TRICLOSAN 3380-34-5 9-TRICOSENE, (E)- 35857-62-6 TRICYCLOHEXYLTIN HYDROXIDE 13121-70-5 4-TRIDECEN-1-OL, ACETATE, (E)- 72269-48-8 4-TRIDECEN-1-OL, ACETATE, (Z)- 65954-19-0 TRIETHANOLAMINE 102-71-6 TRIETHANOLAMINE DODECYLBENZENESULFONATE 27323-41-7 TRIETHYLENE GLYCOL 112-27-6 TRIFLOXYSTROBIN 141517-21-7 TRIFLUMIZOLE 68694-11-1 TRIFLURALIN 1582-09-8 TRIFLUSULFURON-METHYL 126535-15-7 TRIFORINE 26644-46-2 TRIIODOBENZOIC ACID, 2,3,5- 88-82-4 TRIMETHACARB (BROOT) 2686-99-9 2,6,6-TRIMETHYL-BICYCLO(3.1.1)HEPTANE, DIDEHYDRO DERIV. 1330-16-1 2,6,6-TRIMETHYLBICYCLO(3.1.1)-2-HEPT-2-ENE 80-56-8 2,3,5-TRIMETHYLPHENYL METHYLCARBAMATE 2655-15-4 TRINEXAPAC-ETHYL 95266-40-3 TRIPHENYLTIN HYDROXIDE 76-87-9 1,1,1-TRIS(HYDROXYMETHYL)NITROMETHANE 126-11-4 TURPENTINE 8006-64-2 TURPENTINE GUM 9005-90-7 10-UNDECENOIC ACID 112-38-9 UNICONAZOLE (PRUNIT) 83657-17-4 UPPER COAL TAR DISTILLATE 65996-91-0 UREA 57-13-6 VANCIDE TH 7779-27-3 VERNOLATE 1929-77-7 VINCLOZOLIN 50471-44-8 WARFARIN AND SALTS 81-81-2 WARFARIN SODIUM 129-06-6 WINTERGREEN OIL 119-36-8 XYLENE (MIXED ISOMERS) 1330-20-7 XYLENOL 1300-71-6 Z-8-DODECENYL ACETATE 28079-04-1 ZINC 7440-66-6 ZINC CHLORIDE FUME 7646-85-7 ZINC NAPHTHENATE 12001-85-3 ZINC OXIDE 1314-13-2 ZINC PHENOLSULFONATE 127-82-2 ZINC PHOSPHIDE 1314-84-7 ZINC SILICFLUORIDE 16871-71-9 ZINC STEARATE 557-05-1 ZINC SULFATE 7733-02-0 ZINC SULFATE (BASIC) 68813-94-5 ZINC, BIS(1-HYDROXY-2(1H)-PYRIDINETHIONATO-O,S)-, (T-4)- 13463-41-7 ZINEB 12122-67-7 ZIRAM 137-30-4 ZOXAMIDE 156052-68-5

[0348] While this disclosure has been described in connection with what is presently considered to be practical exemplary embodiments, it is to be understood that the present invention is not limited to the disclosed embodiments, but, on the contrary, is intended to cover various modifications and equivalent arrangements. Thus it should be understood that various changes and modifications to the described embodiments herein will be apparent to those skilled in the art. Such changes and modifications can be made without departing from the spirit and scope of the present subject matter and without diminishing its intended advantages. It is therefore intended that such changes and modifications be covered by the appended claims.