Method for stabilizing metal ions in the presence of biofouling organisms

BACKGROUND OF THE INVENTION
Many metal ions are essentially insoluble in aqueous systems having pH's ranging from approximately 6.0 to 9.0. Within this pH range, these metals, including but not limited to iron, zinc, aluminum and manganese, will deposit on heat transfer surfaces causing underdeposit attack.
Recirculating cooling water utilized in industrial applications may contain metal ions, such as iron and manganese which, upon deposition as insoluble salts on heat transfer surfaces, cause decreased operating efficiency and corrosive attack.
These concerns are particularly pertinent to recirculating cooling water systems employed by large utility plants.
Water treatment to prevent scale, corrosion and biological fouling in industrial and municipal aqueous systems is a complicated problem under the best of circumstances. Cooling water in utility plants, for example, may be particularly difficult to treat, especially when the source water contains high concentrations of iron and/or manganese. Also, such plants may be operated at several cycles of concentration. The resulting high levels of iron and manganese pose a challenge to conventional polymer treatment programs designed to stabilize these metals and prevent or inhibit deposits. The added problem of the presence of fouling microorganisms such as bacteria, particularly sulfate reducing bacteria, in the recirculating water generally mandates the use of an aggressive biological treatment program. Balancing the whole range of treatment needs makes it desirable that treatment additives not be antagonistic to one another. Of course, the treatment approach utilized must also take into account the extremes of plant operating parameters such as water quality, pH, cycles of concentration and temperature. All of these factors must be considered to determine the performance limits of any treatment additives utilized.
Polymers and phosphonates, alone and in combination, have been used in the past to stabilize deposit-forming metals ions such as Fe.sup.2+, Fe.sup.3+, and Mn.sup.2+. See for example U.S. Pat. Nos. 4,936,987, 4,640,793, 4,783,267 and 4,552,665. For many cooling towers, chlorine has been used as the biocide. Unfortunately, such biocides may inhibit the ability of polymer and/or phosphonate programs to stabilize metal ions. The instant inventors have surprisingly found that combinations of methylene bis(thiocyanate) and 2-(thiocyanomethylthio)benzothiazole, conventional biocides, enhance the ability of conventional water treatment polymers and/or phosphates to stabilize metal ions. This benefit of the instant biocide compositions is surprising and unexpected.
Hence, a long-felt need in the art of water treatment to find an effective biocide which does not antagonize metal ions stabilization by polymers and/or phosphonates has been met.
The use of methylene bis(thiocyanate) is well known in the art. See, for example, U.S. Pat. Nos. 4,612,328, 3,996,378, 3,300,375 and 3,524,871. However, its surprising effect on the ability of polymers and/or phosphonates to stabilize metal ions is not known or suggested in the art. Calgon product H-102 is a blend of 10% methylene bis(thiocyanate) and 10% 2-(thiocyanomethylthio)benzothiazole, on an active weight basis.
SUMMARY OF THE INVENTION
The present invention is directed to an admixture for the control, prevention and/or inhibition of biofouling and for the stabilization of metal ions, particularly iron and manganese ions, in an aqueous system comprising a) an ethylenically unsaturated water soluble polymer and/or a water soluble phosphonate, b) methylene bis(thiocyanate) and c) 2-(thiocyanomethylthio)benzothiazole.
The present invention is also directed to a method for stabilizing metal ions in the presence of biofouling organisms, and for controlling, preventing and/or inhibiting biofouling comprising adding to an aqueous system containing metal ions and biofouling organisms an effective amount of an admixture comprising a) an ethylenically unsaturated, water soluble polymer and/or a water soluble phosphonate, b) methylene bis(thiocyanate) and c) 2-(thiocyanomethylthio)benzothiazole.
The present invention is further directed to a method for enhancing the ability of water soluble ethylenically unsaturated polymers and/or phosphonates to stabilize metal ions in aqueous systems prone to biofouling comprising adding an effective amount of methylene bis(thiocyanate) and 2-(thiocyanomethylthio)benzothiazole to said polymers and/or phosphonates or to an aqueous system treated with said polymers and/or phosphonates.
As used herein, the term "aqueous system" is meant to include any system containing water, including but not limited to cooling water systems, boiler water systems, desalination systems, gas scrubber systems, blast furnace systems, sewage sludge thermal conditioning systems, reverse osmosis systems, evaporators, paper processing systems, mining circuits, etc. The preferred aqueous systems are cooling water systems, either once-through or closed loop.
The term "stabilizing metal ions", as used herein, refers to the ability of additives to keep metal ions in solution under conditions where, absent the additive, the ions would tend to precipitate out of solution. Thus, these additives either solubilize ions or maintain ions in a soluble state, thereby inhibiting the formation and/or deposition of metallic salts on to the surfaces of aqueous systems.
The term "effective amount", as used herein, refers to the amount of additive necessary to accomplish the objective for which the additive is being used in a given aqueous system.
The instant inventors have discovered that methylene bis(thiocyanate)/2-(thiocyanomethylthio)benzothiazole compositions enchance the ability of conventional water treatment polymers and phosphonates to stabilize metal ions. This use of such compositions is surprising and unexpected.
DETAILED DESCRIPTION OF THE INVENTION
In the broadest sense, the instant invention relates to compositions comprising: a) a water soluble, ethylenically unsaturated polyer and/or a water soluble phosphonate; b) methylene bis(thiocyanate); and c) 2-(thiocyanomethylthio)benzothiazole, wherein the polymer to phosphonate weight ratio of a), if a phosphonate is used, ranges from about 99:1 to about 1:99 and wherein the weight ratio of a) to the sum of b) and c) ranges from about 99:1 to about 1:99. Also, the weight ratio of b) to c) ranges from about 99:1 to about 1:99. Additionally, such compositions may comprise the water of an aqueous system, wherein said water contains metal ions selected from the group consisting of Fe.sup.+2, Fe.sup.+3, Zn.sup.+2, Al.sup.+3, and Mn.sup.+2 and biofouling organisms.
More particularly, the instant invention is directed to a method for stabilizing metal ions in the presence of biofouling organisms and for controlling, preventing and/or inhibiting biofouling, comprising adding to an aqueous system containing metal ions and biofouling organisms an effective amount of a composition comprising: a) a water soluble, ethylenically unsaturated polymer and/or a water soluble phosphonate; b) methylene bis(thiocyanate); and c) 2-(thiocyanomethylthio)benzothiazole.
Further, the instant invention is directed to improved ethylenically unsaturated, water soluble polymer/water soluble phosphonate compositions which additionally comprise methylene bis(thiocyanate) and 2-(thiocyanomethylthio)benzothiazole and to a method for enhancing the ability of polymer and/or phosphonate compositions to stabilize metal ions in aqueous systems comprising adding to such compositions or to aqueous systems in which they are present an effective amount of a composition comprising methylene bis(thiocyanate) and 2-(thiocyanomethylthio)benzothiazole.
The instant invention also relates to an improved method for treating an aqueous system, preferably a recirculating cooling water system, which method comprises adding to the system being treated an effective amount of a composition comprising: a) an ethylenically unsaturated water soluble polymer and/or a water soluble phosphonate; b) methylene bis(thiocyanate); and c) 2-(thiocyanomethylthio)benzothiazole.
Any ethylenically unsaturated, water-soluble polymer may be used as component (a). For example, water soluble polycarboxylates may be used. Such polycarboxylates include, but are not limited to, polymers derived from acrylic acid, methyacrylic acid, vinyl acetic acid, allyl acetic acid, fumaric acid, phosphoric carboxylic acid, maleic acid (and/or its anhydride), itaconic acid, .alpha.-halo acrylic acid and .beta.-carboxyethyl acrylate, alone or in combination, and salts, thereof.
Specific examples of acceptable polymers include homopolymers of acrylic acid or methacrylic acid, copolymers of acrylic acid and methacrylic acid, homopolymers of maleic acid or anhydride, copolymers of any of the above monomers with acrylamide or methacrylamide, hydrolyzed polyacrylamides, copolymers of acrylic acid and hydroxypropyl acrylate, copolymers of maleic acid or anhydride and sulfonated styrene and sulfonated polystyrenes.
A preferred polymer is a water soluble polymer having a weight average molecular weight of less than about 50,000 as determined by low angle laser light scattering comprising i) an unsaturated carboxylic acid selected from the group consisting of acrylic acid, methacrylic acid, .alpha.-halo acrylic acid, maleic acid or anhydride, itaconic acid or anhydride, vinyl acetic acid, allyl acetic acid, fumaric acid, .beta.-carboxyethyl acrylate, their salts, and mixtures thereof, and ii) an unsaturated sulfonic acid selected from the group consisting of 2-acrylamido-2-methylpropylsulfonic acid, 2-methacrylamido-2-methylpropylsulfonic acid, vinyl sulfonic acid, sulfoalkyl acrylate, sulfoalkyl methacrylate, allyl sulfonic acid, methally sulfonic acid, and 3-methacrylamido-2-hydroxypropyl sulfonic acid.
Such preferred polymers may also comprise iii) an unsaturated polyalkylene acid moiety, such as allyl polyethylene glycol, methally polyethylene glycol, polyethylene glycol acrylate, polyethylene glycol methacrylate, methoxy allyl polyethylene oxide, alkoxyallyl polyethylene oxide and the polypropylene equivalents thereof. Also, mixtures of polyethers formed from polyethylene oxide with other polyalkylene oxides, such as propylene or butylene oxide may be used. The polyether chain may be capped with an alkyl, aralkyl, sulfonate or phosphonate group, a metal ion, or uncapped.
If moiety iii) is used, the polymer preferably comprises about 35 to about 90% by weight, i), about 5 to about 40%, by weight, ii), and about 5 to about 40%, by weight, iii).
More preferred polymers are selected from the group consisting of the following water soluble polymers: homopolymers of acrylic acid, homopolymers of methylacrylic acid, homopolymers of maleic acid or anhydride, polymers comprising i) acrylic acid, methacrylic acid or maleic acid and ii) acrylamide or methacrylamide, hydrolyzed polyacrylamides, polymers comprising i) acrylic acid and ii) hydroxy propyl acrylate, polymers comprising i) maleic acid and ii) sulfonated styrene, sulfonated polystyrenes and polymers comprising i) acrylic acid or methacrylic acid and ii) 2-acrylamido-2-methylpropyl sulfonic acid or 2-methacrylamido-2-methylpropyl sulfonic acid. These preferred polymers are water soluble and have molecular weights of less than about 50,000 as determined by light scattering techniques.
The most highly preferred polymers are selected from the group consisting of water-soluble polymers having a weight average molecular weight of less than 50,000 as determined by light scattering comprising:
(i) an unsaturated mono-carboxylic acid selected from the group consisting of acrylic acid and methacrylic acid; and
(ii) an unsaturated sulfonic acid selected from the group consisting of 2-acrylamido-2-methylpropyl sulfonic acid and 2-methacrylamido-2-methylpropyl sulfonic acid;
wherein the weight ratio of (i):(ii) ranges from about 1:4 to about 4:1. Such polymers are commerically available from Calgon Corporation, Pittsburgh, Pa. as TRC-233.RTM..
Any water soluble phosphonate may additionally be used with the above polymers as a portion of component (a). Examples include, but are not limited to, 2-phosphono-1,2,4-tricarboxybutane, amino tri(methylene phosphonic acid), hydroxyethylidene diphosphonic acid, phosphonosuccinic acid, benzene phosphonic acid, 2-aminoethyl phosphonic acid polyamino phosphonates and the like. Additional phosphonates are identified in U.S. Pat. No. 3,837,803, which is hereby incorporated by reference. The preferred phosphonates are 2-phosphono-1,2,4-tricarboxybutane, amino tri(methylene phosphonic acid) and hydroxyethylidene diphosphonic acid, all of which are commercially available. If a phosphonate is used, the ratio of polymer to phosphonate, on an active weight basis, should range from about 99:1 to about 1:99, preferably from about 50:1 to about 1:50, and most preferably from about 20:1 to about 1:20.
Component (b) is methylene bis(thiocyanate) (hereinafter also referred to as MBT). MBT is commerically available from Calgon Corporation, Pittsburgh, Pa. Component (c) is 2-(thiocyanomethylthio)benzothiazole.
The weight ratio of component a) to the sum of components b) and c) in the instant admixtures ranges from about 99:1 to about 1:99, preferably from about 50:1 to about 1:20, and most preferably from about 20:1 to about 1:10. The weight ratio of component b) to component c) should range from about 99:1 to about 1:99, preferably from about 50:1 to about 1:50. Preferably, the amount of b) and c) necessary is determined based upon the characteristics of the aqueous system to be treated, such as its potential for biofouling, and the concentration of metal ions present. It should be noted that virtually any amount of b) and c) is believed to enhance the efficiacy of polymer and/or phosphonate compositions with respect to metal ion stabilization. However, an enhancing amount may be inadequate to control biofouling. Most preferably, the weight ratio of components b) and c) to component a) ranges from about 10:1 to about 1:20.
An effective amount of the instant composition should be used, based on the characteristics of the system being treated. Preferably, at least about 0.1 ppm of the instant composition should be used, more preferably about 1 to about 100 ppm. Order of addition is not believed to be critical. Thus, the individual components of a), and components b) and c) may be added, separately or in some combination thereof, to the aqueous system being treated. Methods of addition are well known to those skilled in the art of water treatment.
Exemplary of the best mode is addition of an effective amount for a given system of a composition comprising:
a) Calgon polymer TRC-233 which is a 60/40 w/w acrylic acid/AMPSA copolymer, and HEDP (hydroxyethylidene diphosphonic acid) at a weight ratio ranging from about 10:1 to about 1:1;
b) MBT; and
c) 2-(thiocyanomethylthio)benzothiazole; wherein the weight ratio of a):b) ranges from about 20:1 to about 1:2 and wherein the weight ratio of b):c) ranges from about 10:1 to about 1:10.

EXAMPLES
The following examples are intended to further demonstrate the invention, They are not, however, intended to limit the invention in any way.
METAL STABILIZATION TESTS
Base Water Preparation
Synthetic recirculating water was prepared based on that of a large utility plant operating at three cycles of concentration. The synthetic cooling tower water contained 9 ppm iron and 3 ppm manganese, with the remaining dissolved solids listed in Table 1. To facilitate the setup of several stabilization tests, the base water was prepared in ten liter batches by adding MgSO.sub.4, CaCl.sub.2.H.sub.2 O, CaSO.sub.4 and NaHPO.sub.4 to 10 L of distilled, deionized water. The weights of these salts are listed in Table 1.
TABLE 1______________________________________SYNTHETIC 3X RECIRCULATING WATER Synthetic Water Ion ConcentrationIon (mg/L) Ion Source g per 10 L______________________________________Mg.sup.++ 39 MgSO.sub.4 1.926Ca.sup.++ 150 CaCl.sub.2.H.sub.2 O 2.664 CaSO.sub.4 2.673PO.sub.4.sup.3- 3 Na.sub.2 HPO.sub.4 0.043HCO.sub.3 305 NaHCO.sub.3 .sup.a 2.754SiO.sub.2 36 Na.sub.2 SiO.sub.3.9H.sub.2 O .sup.b 0.568SO.sub.4.sup.2- 340 MgSO.sub.4 -- CaSO.sub.4 --Cl.sup.- 128.5 CaCl.sub.2.2H.sub.2 O --Na.sup.+ 131 Na.sub.2 HPO.sub.4 -- NaHCO.sub.3 -- Na.sub.2 SiO.sub.3.9H.sub.2 O --______________________________________ .sup.a added from a 84 g NaHCO.sub.3 /L solution (5 ml/1000 ml) .sup.b added from a 34.08 g Na.sub.2 SiO.sub.3.9H.sub.2 O/L solution (5 ml/1000 ml)
Test Procedure
The test apparatus consisted of one liter beakers and gang stirrers. The base water was added to the beakers, followed by 5 mL of 34.8 g/L Na.sub.2 SiO.sub.3.9H.sub.2 O and 5 mL of 1.0M NaHCO.sub.3. The chemical treatment and biocide, if present, were added next from 20 g/L product solutions. The next component added was chlorine to accelerate the oxidation of the metals, especially manganese. It was pipetted from a freshly prepared solution of 190.5 g/L Clorox, standardized before use. Iron and manganese were then added from atomic absorption reference standards (1 mL/1000 mL=1 ppm metal ion). The total test volume was 1000 mL at the end of these additions and the pH was then adjusted to 8.5 with 1.0N NaOH. The beakers were placed under a gang stirrer at room temperature at 60 rpm for 24 hours, after which time they were removed and an aliquot filtered through Whatman 41 filter paper (25 .mu.m filter paper). A 50 mL sample of the filtrate was digested with 0.25 mL concentrated nitric acid and 2.5 mL concentrated HCl.
Atomic absorption analysis was used to determine the concentration of Fe.sup.3+ and Mn.sup.2+. Percent stabilization of the metals was calculated using the following equation: ##EQU1##
A summary of the abbreviations for various polymers, phosphonate and biocides utilized in the examples is shown in Table 2.
TABLE 2______________________________________PRODUCT DESCRIPTIONS ACTIVE % FUNC-ADDITIVE INGREDIENT(S) ACTIVE TION______________________________________AMP Amino tri(methylene 5.0 Phos- phosphonic acid) phonateMBT/ Methylene bis(thiocyanate) 10 BiocideTCMTB and 2-(Thiocyanomethyl- 10 thio)-benzothiazole, available from Calgon as H-102DMAC Dodecyl dimethyl 50 Biocide ammonium chlorideDGH Dodecylguanidine 12.50 Biocide hydrochlorideGLU Gluteraldehyde 45 BiocideDBNPA 2,2-Dibromo-3- 5 Biocide nitrilopropionamidePENETRANT The penetrant is an admixture of various surfactants and polyacrylic acid, available from Calgon as CL-361KATH0N* 5-Chloro-2-methyl-4- 1.15 Biocide isothiazoline-3-one and 2-methyl-4-isothiazoline- 0.35 3-oneNaBr Sodium Bromide 46 BiocideAA/AMPSA Composition containing a 20 Polymer/HEDP 60/40 w/w acrylic acid/ 3.7 Phos- 2-acylamindo-2-methyl phonate propyl sulfonic acid polymer and hydroxyethylidene diphos- phonic acid, commercially available from Calgon as PCL-402AA/AMPSA 60/40 acylic acid/2- 30 Polymer acylamindo 2- methylpropyl sulfonic acid polymer, MW approx. 8200HEDP Hydroxyethylidene 60 Phos- diphosphonic acid phonateMI Methylisothiazoline Biocide______________________________________ (*KATHON is a registered trademark of Rohm and Haas)
EXAMPLES 1-14
The test procedure was followed by employing a polymer and/or phosphonate and one of various biocides including H-102, DMAC, DGH, or DBNPA. The penetrant was also used. The results are shown in Table 3.
TABLE 3______________________________________IRON/MANGANESE STABILIZATION BY H-102 BIOCIDE______________________________________Example PCL-402 PENETRANT H-102 % StabilizationNumber (mg/L) (mg/L) (mg/L) Fe Mn______________________________________1 50 15 21 85 1002 50 15 -- 48 383 50 -- 21 72 874 50 -- -- 27 225 50 5 6 61 59______________________________________ Conditions: Synthetic 3X Recirculating Water: pH 8-9; 9.0 mg/L Fe; 3.0 mg/L Mn; 5.0 mg/L Cl.sub.2 ; 24 Hours; 60 rpm; 60.degree. C.; 25 micron Filtration.
ADDI- % PCL- PENE- TIONAL STABILI-Example 402 TRANT DMAC BIOCIDE ZATIONNumber (mg/L) (mg/L) (mg/L) (mg/L) Fe Mn______________________________________ 6 50 5.1 7.5 -- 71 88 7 50 5.1 6.0 -- 78 89 8 50 5.1 4.5 -- 79 84 9 50 5.1 3.0 -- 84 9110 50 -- 7.5 -- 80 9111 50 5.1 -- -- 100 9512 50 5.1 7.5 15 H-102 92 8913 50 5.1 7.5 15 DBNPA 74 8914 50 5.1 7.5 15 DGH 90 91______________________________________ Conditions: Synthetic 3X Recirculating Water: pH 8.5; R.T.; 24 hrs; 9 mg/ Fe; 3 mg/L Mn; 5 mg/L Cl.sub.2 ; 25 micron Filtration.
EXAMPLES 15-20
The previously described test procedure was followed and the effect of increasing the test period from 24 to 48 hours was examined. As shown in Table 4, neither AA/AMPSA nor the PCL-402 combinations were affected by such an increase in time.
TABLE 4__________________________________________________________________________Effect of Time on Fe.sup.2+ and Mn.sup.2+ Stabilization Corrected % StabilizationExample Number mg/L Treatment Time (Hrs.) PENETRANT (mg/L) mg/L Biocide Fe Mn__________________________________________________________________________15 50 PCL-402 48 5.1 6 MBT 94 100 9 DBNPA16 14.3 AA/AMPSA 48 5.1 6 MBT 92 100 30 PCL-402 9 DBNPA17 35.7 AA/AMPSA 48 5.1 6 H-102 76 85 9 DBNPA18 3.33 HEDP 48 5.1 6 MBT 13 11 9 DBNPA19 35.7 AA/AMPSA 24 5.1 6 MBT 90 89 9 DBNPA20 3.33 HEDP 24 5.1 6 MBT 15 17 9 DBNPA__________________________________________________________________________ Conditions: Synthetic 3X Recirculating Water: pH 8-9; 9.0 mg/L Fe; 3.0 mg/L Mn; 5.0 mg/L Cl.sub.2 ; 24 Hours; 60 rpm; 60.degree. C.; 25 micron Filtration.
EXAMPLES 21-24
The previously described test procedure was followed at 10.degree. C. and at room temperature. As shown in Table 5, the reduced temperature had no impact on iron and manganese stabilization.
TABLE 5__________________________________________________________________________IRON/MANGANESE STABILIZATION COLD WATER STUDYExample Temp. AA/AMPSAA-HEDP PENETRANT H-102 % StabilizationNumber (.degree.C.) (mg/L) (mg/L) (mg/L) Fe Mn__________________________________________________________________________21 10 10 0 0 100 10022 10 10 3.4 4 100 10023 R.T. 10 0 0 97 10024 R.T. 10 3.4 4 96 100__________________________________________________________________________ Conditions: Primary Service Water; pH 7.0; 4 hrs; 5 mg/L Cl.sub.2 ; 3 mg/ Fe; 1 mg/L Mn; 25 micron Filtration.
Table 6, below, summarizes the effects of various biocides on iron and manganese stabilization.
TABLE 6______________________________________EFFECTS OF SELECTED BIOCIDESON FE/MN STABILIZATIONIN 3X RECIRCULATING WATER Effect on StabilizationBiocide(s) Fe Mn______________________________________H-102 + +DMAC - 0DGH 0 0DMAC/MBT 0 0DMAC/DBNPA - 0DMAC/DGH 0 0MI/DBNPA 0 0DGH/DBNPA 0 0______________________________________ (+ = Positive - = Negative 0 = Neutral)

Number	Name	Date
3674457	Wolfson	Jul 1972
3898343	Swered et al.	Aug 1975
4324793	Hagen et l.	Apr 1982
4552665	Ralston et al.	Nov 1985
4612328	Jakubowski	Sep 1986
4719083	Baker et al.	Jan 1988

Method for stabilizing metal ions in the presence of biofouling organisms

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