Method and composition for detecting and quantifying filming amines in liquids

Abstract

A composition and method for the photometric determination of a film-forming amine in liquid by adding an indicator reagent to an aqueous system that is pH dependent, combining a water soluble non-ionic polymer to modify the physical properties of the aqueous system, and adding an acidic buffer to said aqueous system to lower pH and activate said indicator, said water soluble polymer keeping the filming amine/indicator complex in solution despite the acidic buffer and preventing it from precipitating out.

Claims

1. A composition for photometric quantification of filming amines in liquids, comprising: an acidic buffer; and an indicator reagent complex that is reactive that is reactive with filming amines at an acidic pH to produce a color indicative of filming amine concentration, said indicator reagent complex including an indicator reagent and an aqueous modifier configured to prevent the acidic buffer from causing the indicator complex to precipitate, thereby maintaining the indicator complex in solution.

2. The composition for photometric quantification of filming amines in liquids according to claim 1, wherein said indicator reagent comprises rose bengal.

3. The composition for photometric quantification of filming amines in liquids according to claim 2, wherein said indicator reagent comprises rose bengal within a range of from 0.025% to 0.075%.

4. The composition for photometric quantification of filming amines in liquids according to claim 3, wherein said indicator reagent comprises approximately 0.05% rose bengal.

5. The composition for photometric quantification of filming amines in liquids according to claim 1, wherein said acidic buffer comprises citrate.

6. The composition for photometric quantification of filming amines in liquids according to claim 1, wherein said aqueous modifier comprises a hydrophilic polymer.

7. The composition for photometric quantification of filming amines in liquids according to claim 6, wherein said hydrophilic polymer is non-ionic.

8. The composition for photometric quantification of filming amines in liquids according to claim 7, wherein said hydrophilic polymer is plant-derived.

9. The composition for photometric quantification of filming amines in liquids according to claim 7, wherein said hydrophilic polymer is microbial.

10. The composition for photometric quantification of filming amines in liquids according to claim 7, wherein said hydrophilic polymer is synthetic.

11. The composition for photometric quantification of filming amines in liquids according to claim 1, wherein said aqueous modifier comprises any one from a group consisting of hydroxyethylcellulose (HEC), poly(ethylene)oxide (PEO), and hydroxypropyl cellulose (HPC).

12. The composition for photometric quantification of filming amines in liquids according to claim 1, wherein said aqueous modifier comprises hydroxypropyl cellulose (HPC).

13. The composition for photometric quantification of filming amines in liquids according to claim 12, wherein said aqueous modifier comprises approximately 3 g hydroxypropyl cellulose (HPC) per 1000 ml of reagent.

14. The composition for photometric quantification of filming amines in liquids according to claim 1, wherein said acidic buffer comprises citric acid monohydrate.

15. The composition for photometric quantification of filming amines in liquids according to claim 14, wherein said acidic buffer comprises approximately 15% citric acid monohydrate in deionized water.

16. A method for the photometric determination of a film-forming amine in liquid by adding an indicator reagent to an aqueous system that is pH dependent, combining a water soluble non-ionic polymer to modify the rheology of the aqueous system, and adding an acidic buffer to said aqueous system to lower pH and activate said indicator reagent, said water soluble polymer keeping the indicator reagent in solution despite the acidic buffer and preventing the said indicator reagent from precipitating out.

17. The method of claim 16 wherein said acidic buffer comprises citrate.

18. The method of claim 16 wherein said water-soluble polymer comprises any one from a group consisting of hydroxyethylcellulose (HEC), poly(ethylene)oxide (PEO), and hydroxypropyl cellulose (HPC).

Description

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

(1) The present invention is simple, rapid and accurate test method and multicomponent reagent system useful in determining the concentration of filming amines in a liquid sample. The reagent system uses an indicator that is pH dependent, an acidic buffer, plus an aqueous modifier to keep the filming amine complex in solution despite the buffer, preventing it from precipitating out. This complex facilitates a more accurate and repeatable photometric absorbance reading.

(2) In a preferred embodiment the reagent includes rose bengal, the buffer is citrate, and the aqueous modifier is a non-ionic hydrophilic polymer such as, preferably hydroxypropyl cellulose (HPC). While other indicators and buffers may be used, rose bengal and citric acid are preferred.

(3) Other suitable non-ionic hydrophilic polymers according to the invention may be selected from the group consisting of hydroxyethylcellulose (HEC); and poly(ethylene)oxide (PEO). Suitable HPC and HEC polymers are commercially available from Hercules Incorporated, Aqualon Division under the tradenames NATROSOL™ and KLUCEL™, respectively. PEO polymers are available from Dupont Company under the tradename POLYOX™. The right polymer at the right concentration is important to keep the rose bengal/filming amine complex soluble without disrupting the complex. The non-ionic hydrophilic polymer helps to avoid introducing foam or bubbles to the sample which can happen with certain other wetting agents or surfactants. Thus, the presently preferred test reagents includes both an indicator reagent A and buffer reagent B composed as set forth below.

(4) Filming Amine Indicator—Reagent A

(5) 0.05% Rose Bengal

(6) 0.3% Hydroxypropyl Cellulose MW 100,000

(7) 10% Ethyl Alcohol SD-30

(8) 89.65% Deionized Water

(9) To Compose:

(10) Fill a 1 liter container approximately 60% with deionized water (DIW).

(11) Add 3.0 g Hydroxypropyl cellulose MW 100,000.

(12) Mix thoroughly while heating to dissolve.

(13) Let cool completely.

(14) Add 0.5 g Rose Bengal.

(15) Mix thoroughly.

(16) Add 100 ml Ethyl Alcohol SD-30. Mix thoroughly.

(17) Let cool completely.

(18) Dilute to 1000 mL with Deionized Water.

(19) Filming Amine Buffer—Reagent B

(20) 15% Citric Acid Monohydrate

(21) 85% Deionized Water

(22) To Compose:

(23) Fill a 1 liter container approximately 60% with deionized water (DIW).

(24) Add 150 grams Citric Acid Monohydrate.

(25) Stir until dissolved.

(26) Dilute to 1000 mL with Deionized Water.

(27) Adjust the pH to 1.50.

(28) In use, the improved method for detecting and quantifying filming amines in liquid samples using the above-described reagents comprises the following steps.

(29) First: Sample Preparation Rinse and till a 25 mm sample cell to 10 mL mark with liquid sample containing filming amines.

(30) Second: Colorimeter Calibration

(31) Use the foregoing sample cell to zero the colorimeter.

(32) Third: Add and Combine Indicator Reagent A and Buffer Reagent B

(33) Add 0.5 ml of reagent A and 0.5 ml of reagent B to the sample cell. Mix the sample and wait 2 minutes. If filming amines are present in the sample, they will complex with rose bengal forming a pink color. The pink colored complex remains soluble in water thanks to the hydroxypropyl cellulose and does not precipitate.

(34) Fourth: Colorimeter Reading

(35) Place the sample cell in the colorimeter and read absorbance at 560 nm or 570 nm. The absorbance reading is converted to concentration by using a calibration curve obtained by measuring a series of filming amine standard solutions.

(36) Direct Photometric Determination

(37) Direct photometric determination of the colored complexes in aqueous solution is possible. Photometric detection can be made in a simple photometric measuring device using an ordinary LED source. The measuring is executed at a wavelength of between 540 to 580 nm.

(38) The method as described above does not show any selectivity against any other components which might be present within the liquid solution, such as the feed-water, like e.g. ammonia, cyclohexylamine, ethanolamine, morpholine, and the like.

(39) A specific example of the present method and composition is herein described with reference to the below Example and chart:

Example 1

(40) TABLE-US-00001 Test (Z)-N-9-Octadecenylpropane-1,3-diamine (Oleyltrimethylenediamine) (N-Oleyl-1,3-diaminopropane) Range 0-5 ppm Detection 0.13 ppm Limit Precision 0.12 ppm Chemical C21H44N2 Formula Wavelength 570 nm Calibration Y = 3.6132x − 0.1222 R.sup.2 = 0.9969 Reagents Rose Bengal (Filming Amine Reagent - A) Buffer Reagent (Filming Amine Reagent - B) Apparatus 1 × 20 mL cell 2 × 1/2 mL pipette Reagent Filming Amine - Reagent A - Standard Shelf-life, 2 years Shelf-life Filming Amine - Reagent B - Standard Shelf-life, 2 years Procedure 1. Turn on the Colorimeter (Taylor ® TTi ™ 3000 Colorimeter Portable Colorimeter preprogrammed) 2. Select a test menu (ALL TESTS, RECENT TESTS, or FAVORITES) containing Filming Amines using   . 3. Select Filming Amines using .box-tangle-solidup..Math.; then press ENTER ⊙. 4. Rinse and fill 25 mm sample cell to 10 mL mark with sample; then cap. 5. Insert sample cell into sample cell compartment. Align marks per User’s Manual. 6. Select ZERO using   ; then press ENTER ⊙ . Zero will be displayed. 7. Remove sample cell from sample cell compartment; then remove cap. 8. Add 0.5 mL Filming Amines - Reagent A; then swirl to mix. 9. Add 0.5 mL Filming Amines - Reagent B; then cap and swirl to mix thoroughly. 10. Cap and swirl to mix. 11. Place cell in colorimeter. 12. Make sure “TIMER” is highlighted and press the “○” key. If “TIMER” is not highlighted, highlight it using the “   ” keys. 13. With “START” highlighted, press the “○” key. 14. Select “AUTO” 15. After a two-minute wait time the colorimeter will automatically take a reading and the result will be displayed as ppm Oleyltrimethylenediamine. Interferences The following were found to cause interference: Alkalinity ≥ 400 ppm-positive interference Iron Ferric-all levels-negative interference Iron Ferrous ≥ 4 ppm-negative interference Phosphonate-all levels-negative interference Polyphosphate-all levels-negative interference Polymer (PAA)-all levels-negative interference Copper-all levels-negative interference The following were tested up to and found not to cause interference: Chloride-1000 ppm EDTA-20 ppm Molybdate-50 ppm Phosphate-100 ppm Silica-50 ppm Sulfate-500 ppm Sulfite-00 ppm *Based on Interferences causing 10% or more interference Advantages The hydroxypropyl cellulose eliminates precipitate that forms, individual calibration curves were established for three main filming amines that are programed on colorimeter. The present test proved more accurate and precise.

(41) Having now fully set forth the preferred embodiments and certain modifications of the concept underlying the present invention, various other embodiments as well as certain variations and modifications of the embodiments herein shown and described will obviously occur to those skilled in the art upon becoming familiar with said underlying concept. It is to be understood, therefore, that the invention may be practiced otherwise than as specifically set forth in the appended claims.