METHODS AND APPARATUS FOR CONTROLLING OR DESTROYING RED TIDE
20210347662 · 2021-11-11
Inventors
Cpc classification
C02F2203/008
CHEMISTRY; METALLURGY
Y02W10/37
GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
C02F3/348
CHEMISTRY; METALLURGY
C02F3/005
CHEMISTRY; METALLURGY
C02F1/68
CHEMISTRY; METALLURGY
C02F1/4674
CHEMISTRY; METALLURGY
C02F2201/46115
CHEMISTRY; METALLURGY
C02F1/50
CHEMISTRY; METALLURGY
C02F2103/007
CHEMISTRY; METALLURGY
Y02A20/144
GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
C02F2201/008
CHEMISTRY; METALLURGY
C02F1/283
CHEMISTRY; METALLURGY
International classification
C02F1/50
CHEMISTRY; METALLURGY
C02F1/68
CHEMISTRY; METALLURGY
Abstract
A method of controlling red tide in a body of sea water involves treating the body of sea water with a quantity of red tide inhibitor adequate to be effective in resisting growth of the red tide. Corresponding apparatus in the nature of floating vessels containing electrolysis cells are also disclosed.
Claims
1. A method of controlling red tide in a body of sea water comprising providing the body of sea water to be treated, and applying to said body of sea water a quantity of red tide inhibitor adequate to be effective in resisting growth of said red tide.
2. The method of claim 1 including said red tide inhibitor is effective to resist creation of neurotoxins by said red tide.
3. The method of claim 1 including employing as said red tide inhibitor sodium chloride solution.
4. The method of claim 1 including in which said red tide inhibitor is employed by spreading at least one solid salt on the red tide selected from the group consisting of sodium chloride, rock salt, calcium oxide, calcium hydroxide, calcium carbonate and calcium sulfate.
5. The method of claim 1 including in which said red tide inhibitor is employed by spreading on the red tide at least one of the group consisting of cold water and ice chips.
6. The method of claim 1 including employing symbiotic microorganisms generating signaling molecules which cause the red tide to cease proliferation.
7. The method of claim 1 including employing as said red tide inhibitor an application of a solid absorbent for red tide neurotoxins.
8. The method of claim 7 including in which said solid absorbent is selected from the group consisting of activated carbon and zeolites.
9. The method of claim 1 including said red tide inhibitor includes a dye.
10. A method of controlling red tide in a body of sea water comprising providing the body of sea water to be treated, and applying means to electrolyze said body of seawater employing electrolysis cells comprising an anode and a cathode in a leaking electrochemical cell.
11. The method of claim 10 including said cells are connected to a DC power source.
12. The method of claim 10 including said anode being a sacrificial anode.
13. The method of claim 10 including said electrolysis cell is a composite consisting of an anode, a cathode and a thin film separator disposed therebetween.
14. The method of claim 1 including providing a floating vessel, having a plurality of electrolysis cells for receiving said body of sea water, and treating said body of sea water.
15. The method of claim 14 including employing open electrolysis cells as said electrolysis cells.
16. The method of claim 10 including said anode having a dimensionally stable anode screen chosen from the group consisting of platinized titanium, ruthenium catalyzed titanium, graphite cloth and conductive titanium oxide.
17. The method of claim 10 including said anode being a sacrificial anode screen chosen from the group consisting of copper, nickel, brass and zinc.
18. The method of claim 10 including resisting undesired passivation and filming by periodically effecting current reversal by employing alternating current.
19. The method of claim 1 including providing a red tide concentration monitoring device.
20. A floating vessel for processing red tide contained within a body of sea water to be treated comprising, subsequently said floating vessel being structured to process red tide containing sea water in order to control the same, and said floating vessel having a plurality of electrolysis cells, and said vessel structured to have water flow through the vessel and be processed by red tide inhibitors, and subsequently to have the treated water discharged from the vessel.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
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DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0060] As employed herein, the term “red tide” will refer to the Karina brevis incipient blooms and blooms along with their toxic products which serve to establish in sea water conditions which kill fish and other sea life and have a negative impact on health of human beings and the environment.
[0061] The term “body of water” means sea water which contains K. brevis and its associated neurotoxins.
[0062] As employed herein, the term “red tide inhibitor” means solid or liquid materials which are introduced to sea water containing K. brevis and incipient blooms or blooms which are sought to be controlled or destroyed. This may be accomplished by spraying, delivering from a crop duster or a floating vessel, for example.
[0063] The term “red tide inhibitor” shall include, but not be limited to, the use of sodium chloride as a brine solution or in solid form. It also includes salts of other cations and ions as well as non-ionic additives such as activated carbons, clays and modified clays.
[0064] Microscopic observation has led to the conclusion that at low salinity K. brevis cells grow in size, possibly through the intake of water through its cell walls, resulting from osmotic pressure. A published independent research study has shown that osmotic stress does not trigger brevetoxin production or that brevetoxins have an osmoregulatory function.
[0065] It has been observed that “salinity is the major environmental factor that determines the distribution and performance of marine K. brevis”. One aspect of the present invention is based in part on providing increased salinity concentrations to effectively control K. brevis proliferation.
[0066] In one embodiment of the invention, blooms and incipient blooms are treated with a red tide inhibitor which is a concentrated saline solution or solid salt itself such that K. brevis growth is inhibited, causing the K. brevis to go into a hibernating state forming cysts, or causes the K. brevis to sink to the bottom or die.
[0067] Red tide inhibitors include agents other than sodium chloride solutions or solid salt. These chemicals include salts that are otherwise nontoxic at low concentrations to sea life like fish, shellfish, manatees, dolphins, sharks, turtles, birds etc. These chemicals should be commercially available in large quantity and at relatively low cost.
[0068] Useful salts include salts comprised of cations like sodium, potassium, calcium, magnesium, iron and quaternary ammonium, and may also include anions including chloride, hydroxide, sulfate, carbonate, acetate, propionate, fluoride, hypochlorite, chlorate, phosphate and others that are non-toxic and available in aqueous solution or solid form. Poorly soluble but effective salts like carbonates and sulfates have beneficial effects by acting more slowly with the K. brevis and at greater depths.
[0069] Methods of distributing red tide inhibitors include surface spraying, spreading from the air above using helicopters or other aircraft types. Aircraft are outfitted with equipment similar to that used for agricultural applications of fertilizer or biocides. Control can also be accomplished using ships such as barges and boats equipped with surface spraying technology such as equipment similarly used for deicing roads, as well as farm type sprayers and spreaders pulled behind tractors. Additional equipment could be provided for injection to promote turbulence to control K. brevis below the surface.
[0070] This invention includes the use of various salts or salt solutions and selected additives. Such additives include bacteria known to attack K. brevis but are otherwise harmless, signaling chemicals causing the K. brevis to go into hibernation and cease or stop proliferation, soluble non-toxic dyes or harmless fluorescent dyes to show and highlight where red tide inhibition has occurred. Substances which block sunlight at certain wavelengths may be included such that K. brevis proliferation is inhibited or ceases. In the category of additives additionally are high surface area activated carbon particles which provide the dual benefits of blocking sunlight and adsorbing neurotoxin byproducts.
[0071] K. brevis control can also be accomplished by rapidly changing the pH of the K. brevis environment, for example by treatment with an acid like acetic acid (vinegar) or by a base like calcium hydroxide or calcium oxide. Additionally, the calcium cation aids also in salting. Control methods involving changing pH works best directly on blooms. Normally the surface pH of seawater is about 7. With the appropriate choice of additive the pH of the surface waters will increase over the short term of treatment in the range of pH 8.5 to 12 and most appropriately to about pH 10.
[0072] Other embodiments of this invention employ additives, including clay, seaweed particulates and activated carbons which attach to K. brevis and/or serve as an absorbent for neurotoxins such as the brevetoxins from red tide. Remedial additives also include those which limit sunlight exposure, including certain dyes. Particulates such as clay, seaweed and activated carbons are especially beneficial since particulates can drag the red tide inhibitors deeper into areas where K. brevis exists below the surface. Combinations of these additives may be employed. As an example of an effective combination, activated carbon is combined with a dye, a salting cation and a pH changing chemical.
[0073] To take advantage of K. brevis's temperature range sensitivity in order to control proliferation, the invention includes controlling the temperature immediately near or on the water surface. For example, surface cooling is accomplished by blowing cold air (below 59 degrees F.), spreading ice chips, spraying cold water, or refrigerating the bottom of a vessel. Likewise, surface heating of the sea water may be accomplished by spraying hot water or providing a microwave heating means on the bottom of a vessel. In addition, to ensure cessation of K. brevis proliferation, optional red tide inhibitor and other additives are provided simultaneously.
[0074] While it is preferred to apply the present invention to waters with low K. brevis counts, the invention is applicable to incipient blooms and areas in full bloom, recognizing the cost of control will rise as the concentration and the extent of K. brevis increases. Signaling molecules generated and dispersing in the waters, as a result of employing the above control methods, are expected to influence large adjacent areas of K. brevis blooms causing hibernation or death of the K. brevis.
[0075] A further embodiment of this invention are electrochemical methods to control K. brevis growth, thereby limiting or stopping the formation of associated neurotoxins.
[0076] Art references to electrochemical technology for pollution control exist. For example, “Electrochemistry for a Cleaner Environment,” edited by Genders and Weinberg, published in 1992 by The Electrosynthesis Company, Inc. Lancaster, N.Y., describes electrochemical cell designs, both monopolar and bipolar, electrode materials, methods, and conditions, for electrochemically treating pollutants. Another publication is entitled, “Industrial Electrochemistry,” by Pletcher and Walsh, published by Blackie Academic & Professional, NY.
[0077] The publication entitled, Electrochemistry for a Cleaner Environment, edited by Genders and Weinberg, 1992 describes many methods and solutions for electrochemically treating pollutants which could include K. brevis.
[0078] An additional embodiment of the present invention is the use of electrolysis cell designs which purposefully have an open cell design or “leak”, thereby simplifying cell design, lowering cost and avoiding fouling issues while minimizing deposits. Zappi and Weinberg, U.S. Pat. No. 6,315,886, describes such cell designs and their uses. The drawing accompanying in this application and the associated text describe a leaking cell design and a set of internal components. In the practice of this invention, in one example, a floating vessel such as a barge or ship is equipped with one or more leaking electrochemical cells, operating as the vessel moves and controls the proliferation of K. brevis.
[0079] The invention described herein includes electrochemical processing methods for control of K. brevis. In operation, a direct current is applied to an electrolysis cell, causing reactions to occur at both the positively charged anode and the negatively charged cathode. At the anode, oxidation processes can occur such as oxygen evolution, destruction of the K. brevis and toxic substances like neurotoxins. At the cathode, reduction processes can occur such as formation of hydrogen gas, caustic and reduction of toxic substances. Formation of caustic will cause a rise in alkalinity which will kill K. brevis. In brackish or seawater, chlorine can be produced at the anode, as well as hypochlorite by reaction of chlorine with the aqueous solution. Those skilled in the art, will choose the appropriate electrode materials, electrolysis cell designs, and other parameters such as current density and flow rate to use to affect the desired process outcome. The electrolysis current density is adjusted manually or automatically by those skilled in the art to the concentration of algae in the seawater, higher current densities chosen for higher algae concentrations. Thus the current density range may be in the range of milliamperes per square meter of electrode surface area to amperes per square meter, the upper limit chosen to minimize chlorine formation at the anode.
[0080]
[0081] In situations where space is limited, flow through the barge may be established by pumping by an onboard system. If desired, and a preferred embodiment, the whole of the barge may be established as an anode so that as the barge moves through the water it will treat the K. brevis.
[0082] Referring in further detail to
[0083]
[0084] A Leaking Electrolysis Processing System for K. brevis control incorporated in a floating vessel such as a barge 2 or Ship will be considered.
[0085] For control of K. brevis in a large body of water, such as the Gulf of Mexico, for example, floating barge 2, a vessel such as a floating barge or ship is converted into an electrochemical processing system. The electrochemical system consists of the following design elements:
[0086] (1) To the hull of the floating vessel is attached a chemically and electrochemically stable cathode material such as titanium, stainless steel, nickel, copper, graphite as well as others;
[0087] (2) Layered and attached to the cathode material is a thin stable microporous separator which may be made of materials such as polypropylene, polyethylene, glass fiber, as well as others, chosen to minimize ohmic drop in the resultant composite;
[0088] (3) Two types of anode materials are utilized each with its own characteristics:
a dimensionally stable anode screen or mesh chosen from the group of titanium, platinum catalyzed titanium, ruthenium catalyzed titanium, graphite cloth, conductive titanium oxide, as well as others are anode materials deposited directly on the separator material, for example by vapor deposition;
[0089] a sacrificial anode screen or mesh, chosen from the group of copper, nickel, brass, zinc as well as others and their alloys, is attached to the free-side of the separator;
[0090] (4) Electrical connections are made to the cathode and anode elements;
[0091] (5) Aboard the vessel is a DC power system of a size capable of powering the composite so that electrolysis occurs at the desired rate (expressed as current density), the rate reflecting the K. brevis concentration and other factors including the conductivity of the body of water;
[0092] (6) The electrical output of the DC unit is powered by a fuel-fed generator, or from a solar panel array or both;
[0093] (7) The current density is changed automatically in the range from zero to a value established analytically based on the K. brevis cell count and other operational factors;
[0094] (8) Analytical equipment aboard the vessel continuously monitors such factors as the presence and kill rate of the K. brevis, the destruction of any released neurotoxic chemicals, hypochlorite generation, corrosion products, especially from type (b) sacrificial electrodes, as well as other analyses needed;
[0095] (9) For composite electrodes incorporating type (b) anodes, provision is made for continuously feeding fresh sacrificial metal screen or mesh from aboard the vessel as it corrodes away;
[0096] (10) An alternative embodiment to this invention is dragging of the electrified electrode-separator composite freely through the water instead of attachment to the bottom of the vessel;
[0097] (11) The vessel may be totally automated for periods of time, requiring minimal or no manpower, but continuously reporting conditions and data to shore personnel;
[0098] (12) Additional elements may be provided as needed, such as removing adherent films growing on the anode, clearing obstructions such as branches and seaweeds, and means to keep fish at a distance.
[0099] The K. brevis content would be measured at the input and output of the cell for current control purposes and to confirm effectiveness.
[0100]
[0101]
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[0104] Sacrificial anodes metal particulate can be fed from a continually filled hopper or can be sheet metal fed from a supply roller to a take-up roller.
[0105] Compared to the use of bleach being sprayed to control algae, electrochemical generation of hypochlorite this oxidant in a more manageable and controlled in localized areas.
[0106] Alternatively, the source of the feed could be sea water at the salinity of the vessel's marine environment. The electrogenerated aqueous hypochlorite solution is then dispersed in the K. brevis proliferation area, when analysis shows the K. brevis to be at low concentrations, on the incipient bloom area where the K. brevis is at higher concentrations, or on the bloom itself. Additives, for example, dyes, to delineate areas of treatment, or emulsifiers to spread red tide inhibitor more uniformly, can be added to the outflow of the leaking electrochemical cells. Activated carbons are also useful as additives to adsorb and minimize brevetoxins.
[0107] Depending on the application, electrolysis cell designs may include separators or ion exchange membranes to separate anode and cathode compartments as well as turbulence promoting internal structures. However, such separated electrochemical cell designs, in general, have a number of limitations, including separator and membrane fouling, buildup of deposits on cell parts and walls, and costly maintenance. The present invention avoids the use of ion exchange membranes in most applications, but does provide for separation of anodes and cathodes as well as turbulence flow promoters.
[0108] Under certain conditions, applying electrolysis, the K. brevis and its toxic byproducts are directly oxidized or reduced at the electrodes, thereby killing the K. brevis as well as destroying toxic byproducts, for example in the case of K. brevis, the brevetoxins. During electrolysis passivation or filming of electrodes may occur by deposition for example, of organic byproducts, causing an increase in ohmic resistance and loss of efficiency. Applying periodic current reversal or superimposed alternating current can effectively counter passivation and filming. Sensors can automate current reversal when needed.
[0109] Well-known to those skilled in the art are methods and equipment for electrochemical generation of hypochlorite solution for disinfection of saline water, for example, for swimming pools and for control of K. brevis growth in boiler water systems, to name only a few applications. Choice of appropriate electrically conductive anode materials that inhibit or minimize chlorine and hypochlorite production include but are not limited to anodes with high chlorine overpotential, including uncatalyzed titanium and niobium and alloys thereof, as well as various kinds of conductive carbons including graphite and diamond as well as conductive titanium oxides.
[0110] Anodes can also include slowly dissolving “sacrificial” metal anodes, such as steel, iron, copper, nickel, aluminum, magnesium, zinc, titanium and alloys thereof. Sacrificial anodes are useful in practicing the art for a number of reasons: avoiding or minimizing chlorine and hypochlorite generation, generation of the metal salt aiding red tide inhibition as the anode corrodes, and their relatively much lower cost compared to noble metal catalyzed anodes, such as Dimensionally Stable Anodes (“DSA's”). Sacrificial anode metals can be in sheet form, porous or non-porous and can be in the form of metal particulates such as shavings, dust, spheres, etc., fed continuously into a hopper connected electrically to the positive terminal of the DC power source and replenished as the metal in the hopper undergoes anodic corrosion.
[0111] Cathode materials include but are not limited to titanium, iron, nickel, aluminum, zinc, copper, metal alloys thereof and various conductive carbons.
[0112] An additional embodiment of the present invention is the use of electrolysis cell designs which purposefully have an open cell design or “leak”, thereby simplifying cell design, lowering cost and avoiding fouling issues while minimizing deposits. Zappi and Weinberg, U.S. Pat. No. 6,315,886, describes such cell designs and their uses. Accompanying drawings in this application depict a leaking cell design and a set of internal components. In the practice of this invention, in one example, a floating vessel such as a barge or ship is equipped with one or more leaking electrochemical cells, operating as the vessel moves and controls the proliferation of K. brevis.
[0113] A further embodiment of the present invention is the application of composite electrode materials consisting for example of metallic screens sandwiching a microporous separator. As an example, a composite sandwich can be constructed of titanium screen anodes and cathodes separated by an inert porous material such as polypropylene to keep the electrodes from shorting but maintaining a low ohmic resistance when in use in K. brevis infested waters. Direct current powered composites can be formed into sheets of various lengths and widths which can float on the water or dragged along the surface or deeper to kill the K. brevis.
[0114] Open or leaking electrochemical cell designs powered by a DC power source can be used for electrochemical generation of hypochlorite (bleach) solution from sea water, with the hypochlorite effluent then used to kill the K. brevis. Hypochlorite solution produced in this way should be at a low enough concentration sufficient to kill K. brevis, but insufficient to harm or kill fish and other wildlife.
[0115] Compared to the prior art where bleach solution is sprayed to control K. brevis, electrochemical generation of hypochlorite provides this oxidant in a more manageable localized space.
[0116] Alternatively, the source of the feed could be sea water at the salinity of the vessel's marine environment. The electrogenerated aqueous hypochlorite solution is then dispersed in the K. brevis proliferation area, when analysis shows the K. brevis to be at low concentrations, on the incipient bloom area where the K. brevis is at higher concentrations, or on the bloom itself. Additives, for example, dyes, to delineate areas of treatment, or emulsifiers to spread red tide inhibitors more uniformly, can be added to the outflow of the leaking electrochemical cells. Activated carbons are also useful as additives to adsorb and minimize brevetoxins.
[0117] An advantageous embodiment of the invention is to pass marine water infested with K. brevis through one or more leaking cell systems. Direct electrochemical control of K. brevis in this manner would also destroy toxic byproducts and other substances in the water, such as, for example brevetoxins, in the case of red tide. Appropriate choices of anode and cathode materials, current density and flow rate would be employed.
[0118] Anode materials may be non-porous; however, higher porosity anode materials can be used to increase the contact area for greater electrochemical efficiency. Such higher surface anode materials could be in the form of metal screens as well as in the form of conductive particles including metal filings and metal balls. In the case of sacrificial anode materials for example using iron filings, means would be provided in the cell design with a corrosion-stable metal or graphite connector to the filings and for continuous addition of fresh iron filings to the anode compartment as anodic corrosion proceeds.
[0119] Irrespective of the actual mechanisms of destruction of K. brevis and toxic byproducts, the appropriate choices of anode and cathode materials can cause direct oxidation of the K. brevis and the toxic byproducts at the anode, in situ destruction of these marine species, destruction by generation of trace hypochlorite, or generation of a powerful oxidizing agent such as peroxide, ozone or chlorate. Importantly, direct electrolysis of K. brevis laden sea water results in killing of the K. brevis and destruction of its toxic byproducts, such that the effluent from the leaking electrolysis equipment is made harmless to sea life.
[0120] Buildup on the electrodes of slimes as well as organic and inorganic deposits can be removed by periodic current reversal.
[0121] DC generators, solar cells, or rechargeable batteries could provide the necessary electricity to power the electrolysis equipment described hereinbefore.
[0122] The present disclosure provides:
1. A method of controlling red tide in a body of sea water comprising
[0123] providing the body of sea water to be treated, and
[0124] applying to said body of sea water a quantity of red tide inhibitor adequate to be effective in resisting growth of said red tide.
2. The method of paragraph 1 including
[0125] said red tide inhibitor is effective to resist creation of neurotoxins by said red tide.
3. The method of paragraph 1 including
[0126] employing as said red tide inhibitor sodium chloride solution.
4. The method of paragraph 1 including
[0127] in which said red tide inhibitor is employed by spreading at least one solid salt on the red tide selected from the group consisting of sodium chloride, rock salt, calcium oxide, calcium hydroxide, calcium carbonate and calcium sulfate.
5. The method of paragraph 1 including
[0128] employing said red tide inhibitor when said sea water is at a temperature of about 59° F. to 86° F.
6. The method of paragraph 1 including
[0129] by said method resisting blooming of said red tide.
7. The method of paragraph 1 including
[0130] employing symbiotic microorganisms generating signaling molecules which cause the red tide to cease proliferation.
8. The method of paragraph 1 including
[0131] distributing as said red tide inhibitor bacteria which will control the red tide.
9. The method of paragraph 1 including
[0132] employing as said red tide inhibitor an application of a solid absorbent for red tide neurotoxins.
10. The method of paragraph 9 including
[0133] in which said solid absorbent is selected from the group consisting of activated carbon and zeolites.
11. The method of paragraph 1 including
[0134] said red tide inhibitor includes a dye.
12. The method of paragraph 1 including
[0135] employing as said red tide inhibitor, a material selected from the group consisting of a concentrated saline solution or solid salt thereof.
13. The method of paragraph 1 including
[0136] employing as additives in treating said body of sea water at least one material selected from the group consisting of concentrated solutions of activated carbon, magnesium sulfate and copper sulfate.
14. The method of paragraph 1 including
[0137] said red tide inhibitor being tetramethylammonium chloride solution.
15. The method of paragraph 1 including
[0138] employing a method of electrolysis control of said red tide in a body of water, using an anode and a cathode contained in a leaking electrochemical cell.
16. The method of paragraph 15 including
[0139] said cells are connected to a DC power source.
17. The method of paragraph 15 including
[0140] said anode being a sacrificial anode.
18. The method of paragraph 15 including
[0141] said electrolysis cell is a composite consisting of an anode, a cathode and a thin film separator disposed therebetween.
19. The method of paragraph 15 including
[0142] wherein said cell is powered by an AC power source.
20. The method of paragraph 1 including
[0143] providing a floating vessel, having a plurality of electrolysis cells for receiving said body of sea water, and
[0144] treating said body of sea water.
21. The method of paragraph 20 including
[0145] said vessel is a vessel having said electrolysis cells operatively associated therewith, and
[0146] said vessel having power means for moving said vessel through said body of sea water.
22. The method of paragraph 20 including
[0147] said vessel being a floating barge.
23. The method of paragraph 20 including
[0148] introducing said sea water into said electrolysis cells and processing said sea water by treating it with said red tide inhibitor.
24. The method of paragraph 23 including
[0149] subsequent to said treating removing said processed sea water from said vessel.
25 The method of paragraph 20 including
[0150] establishing said flow of said body of sea water through said electrolysis cells to process the same and subsequently discharge the same and,
[0151] said flow of said sea water being effected, at least in part, through movement of said vessel.
26. The method of paragraph 20 including
[0152] employing open electrolysis cells as said electrolysis cells.
27. The method of paragraph 21 including
[0153] said vessel being a pontoon boat having a pair of pontoons, and
[0154] said electrolysis cells being secured to said vessel in a position disposed generally between said pontoons.
28. The method of paragraph 20 including
[0155] said vessel having a deck with said electrolysis cells secured to said deck.
29. The method of paragraph 20 including
[0156] said electrolysis cells having at least one anode, and
[0157] said anode being operated by DC power.
30. The method of paragraph 20 including
[0158] said vessel being a floating vessel which remains substantially stationary during processing of said sea water.
31. The method of paragraph 29 including
[0159] said anode having a dimensionally stable anode screen chosen from the group consisting of platinized titanium, ruthenium catalyzed titanium, graphite cloth and conductive titanium oxide.
32. The method of paragraph 29 including
[0160] said anode being a sacrificial anode screen chosen from the group consisting of copper, nickel, brass and zinc.
33. The method of paragraph 20 including
[0161] resisting undesired passivation and filming by periodically effecting current reversal or superimposed alternating current.
34. A floating vessel for processing red tide contained within a body of sea water to be treated comprising,
[0162] subsequently said floating vessel being structured to process red tide containing sea water in order to control the same, and
[0163] said floating vessel having a plurality of electrolysis cells, and
[0164] said vessel structured to have water flow through the vessel and be processed by red tide inhibitors, and subsequently to have the treated water discharged from the vessel.
35. The vessel of paragraph 34 including
[0165] said vessel structured to take in said sea water when the vessel is in motion.
36. The vessel of paragraph 34 including
[0166] said vessel being structured to have said sea water flow through said vessel under the influence of movement of said vessel.
37. The vessel of paragraph 34 including
[0167] said vessel being a floating barge which is structured to be stationery during said processing of said sea water by said electrolysis cells.
38. The vessel of paragraph 34 including
[0168] said electrolysis cells being open cells.
39. The vessel of paragraph 34 including
[0169] said vessel being a pontoon boat and said electrolysis cells being secured to said vessel in a position to be immersed in said body of sea water during treating of said sea water.
40. The vessel of paragraph 34 including
[0170] said vessel being a pontoon boat having a pair of relatively spaced pontoons, and a deck,
[0171] said pontoons secured to the underside thereof, and
[0172] said electrolysis cells being secured to said pontoon boat, and
[0173] said electrolysis cells being disposed in the space defined by the underside of the deck and between said vessel.
41. The vessel of paragraph 34 including
[0174] said electrolysis cells being structured to resist formation of red cell blooms and resultant toxic materials.
42. The vessel of paragraph 34 including
[0175] said apparatus being structured to be energized by AC current.
43. The method of claim 1 including providing a red tide concentration monitoring device.
44. The method of claim 43, wherein the amount of red tide inhibitor is automatically adjusted to the measured red tide concentration.
EXAMPLES
[0176] Experiments were performed to determine the K. brevis count with various red tide inhibitors.
[0177] A microscope with magnification up to 2500 times, was used along with a gridded Sedgewick-Rafter counting slide to record K. brevis cell counts. Testing was performed on Gulf of Mexico sea water containing K. brevis with an initial K. brevis cell count of at least 1 million K. brevis cells per liter. Test tubes contained 10 ml. each of this sea water, to which the following salts and other chemicals were added. For a concentrated solution of the additive, one drop is added and for solid additives, 5 mg is added. The test tubes contents containing the additives were gently mixed and then counts tabulated after two minutes.
[0178] Table 1 identifies the additives tested and the resultant cell count.
TABLE-US-00001 TABLE 1 Experiment Number Additive Cell Count 1 Commercial bleach solution None 2 Concentrated salt solution None 3 Finely ground solid salt None 4 Concentrated calcium sulfate solution None 5 Concentrated magnesium sulfate solution None 6 Concentrated copper sulfate solution None 7 High surface area activated carbon Very few 8 Household acetic acid (vinegar) None 9 Solid calcium oxide None 10 Dilute methylene blue solution Very few 11 Combination of dye, activated carbon and None finely ground salt crystals 12 Combination of solutions of concentrated None calcium sulfate and copper sulfate with activated carbon
[0179] The above experiments illustrate the effectiveness of red tide inhibitors, the use of activated carbon and the application of combinations of additives.
[0180] An additional list of materials which can be used in red tide inhibition is shown in Table 2.
TABLE-US-00002 TABLE 2 Additive Explanation Experimental Results* Cold Water, 40° F. Change temperature from normal range No living K. brevis for sustainability of K. brevis Crushed Ice Change temperature from normal range No living K. brevis for sustainability of K. brevis Commercial bleach solution Repeat literature results that bleach No living K. brevis kills K. brevis Clay Repeat literature results that clay No living K. brevis removes or kills K. brevis Concentrated salt (NaCl) Change salinity from normal range for No living K. brevis solution sustainability of K. brevis Finely ground solid salt (NaCl) Change salinity from normal range for No living K. brevis sustainability of K. brevis Concentrated calcium sulfate Test positively charged cationic No living K. brevis solution additives Concentrated magnesium Test positively charged cationic No living K. brevis sulfate solution additives Concentrated copper sulfate Repeat literature results that copper No living K. brevis solution sulfate removes or kills K. brevis Concentrated sulfate salts of Test positively charged cationic No living K. brevis iron and aluminum additives High surface area activated Test if activated carbon removes or No living K. brevis carbon kills K. brevis; use of activated carbon to absorb toxic substances Ground BioChar** solids Test if BioChar removes or kills K. No living K. brevis brevis Household vinegar (acetic acid) Test change of solution pH No living K. brevis Concentrated sodium carbonate Test change of solution pH solution Concentrated lime solution Test change of solution pH No living K. brevis (calcium hydroxide solution) Concentrated calcium sulfate Test positively charged cationic No living K. brevis solution additives Concentrated methylammonium Test cationic ammonium additives No living K. brevis chloride solution Concentrated Test cationic ammonium additives No living K. brevis tetamethylammonium chloride solution Dilute methylene blue dye Test cationic organic dyes No living K. brevis solution Combination of cationic dye, Test combinations of additives No living K. brevis activated carbon and finely ground of d salt crystals Combination of solution of Test combinations of additives No living K. brevis concentrated calcium sulfate and activated carbon *Experimental Results, using microscopy and a microscope slide with a drop of Gulf of Mexico marine water containing at least hundreds of living K. brevis organisms to start. If the additive in solution form a droplet of the additive was added to the K. brevis containing droplet on the microscope slide. If the additive was in solid form, about 1 to 0 mg of the solid was added to the K. brevis containing droplet. **BioChar is a charcoal-like form of carbon produced by pyrolysis of biomass in absence of oxygen.
[0181] Experimental results listed in Table 2 demonstrate that all these additives and combinations killed K. brevis.
[0182] A 250 ml single compartment electrolysis cell was used containing an anode, a cathode and Ag/AgCl reference electrode to measure the anode potential. A DC power supply along with a digital voltmeter and magnetic mixing were used. The electrolysis cell was filled with Gulf of Mexico water seeded with K. brevis such that a K. brevis cell count of at least 1 million per liter. In each case the cathode was a graphite rod and the anode materials included: graphite, copper, stainless steel, aluminum, zinc, platinized titanium and uncatalyzed titanium. Electrolysis was conducted for 10 minutes with gentle stirring.
[0183] Anodes of graphite, platinized titanium and uncatalyzed titanium evolved gas bubbles on polarization and the aqueous electrolyzate had the distinct odor of bleach. In contrast copper, aluminum and zinc anodes evolved no gas on polarization. These sacrificial anode metals exhibited some corrosion. The electrolyzate had a precipitate but had no evidence of hypochlorite formation by smell and by testing with hypochloritetest papers. Electrolysis tests were performed employing a composite in a leaky cell configuration.
(a) A titanium screen serving as the cathode in a tightly layered composite configuration is covered on both sides with a microporous polymer, with outer layers attached to the polymer of high surface area graphite cloth serving as the anode material. This composite cell is contained in a tube open at both ends. Electrical connection is made to a DC power supply and sea water containing K. brevis was pumped into a tube as electrolysis proceeded. Microscopic analysis of the effluent shows no K. brevis was present.
(b) The same composite electrolysis cell configuration and open-ended tubing was employed as in (a) above, except that the anode material was a sacrificial metal. Pumped into the leaky cell is sea water containing K. brevis. Electrolysis followed by microscopic analysis of the electrolyzate showed no K. brevis present.
REFERENCES
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[0200] All publications and patents referred to herein are incorporated by reference. Various modifications and variations of the described subject matter will be apparent to those skilled in the art without departing from the scope and spirit of the invention. Although the invention has been described in connection with specific embodiments, it should be understood that the invention as claimed should not be unduly limited to these embodiments. Indeed, various modifications for carrying out the invention are obvious to those skilled in the art and are intended to be within the scope of the following claims.