AU2007308351A1 - Controlled Foam Alkyl Quat Formulations - Google Patents

Controlled Foam Alkyl Quat Formulations Download PDF

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Publication number
AU2007308351A1
AU2007308351A1 AU2007308351A AU2007308351A AU2007308351A1 AU 2007308351 A1 AU2007308351 A1 AU 2007308351A1 AU 2007308351 A AU2007308351 A AU 2007308351A AU 2007308351 A AU2007308351 A AU 2007308351A AU 2007308351 A1 AU2007308351 A1 AU 2007308351A1
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anionic surfactant
quaternary ammonium
compound
branched
alkyl
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AU2007308351B2 (en
Inventor
Michael Lutzeler
Volker Ranft
Philip Gerdon Sweeny
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Innovative Water Care LLC
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Lonza AG
Lonza LLC
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D19/00Degasification of liquids
    • B01D19/02Foam dispersion or prevention
    • B01D19/04Foam dispersion or prevention by addition of chemical substances
    • B01D19/0404Foam dispersion or prevention by addition of chemical substances characterised by the nature of the chemical substance
    • B01D19/0422Foam dispersion or prevention by addition of chemical substances characterised by the nature of the chemical substance compounds containing S-atoms
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N33/00Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
    • A01N33/02Amines; Quaternary ammonium compounds
    • A01N33/12Quaternary ammonium compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2/00Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
    • A61L2/02Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor using physical phenomena
    • A61L2/08Radiation
    • A61L2/10Ultraviolet radiation
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2/00Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
    • A61L2/16Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor using chemical substances
    • A61L2/18Liquid substances or solutions comprising solids or dissolved gases
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D19/00Degasification of liquids
    • B01D19/02Foam dispersion or prevention
    • B01D19/04Foam dispersion or prevention by addition of chemical substances
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D19/00Degasification of liquids
    • B01D19/02Foam dispersion or prevention
    • B01D19/04Foam dispersion or prevention by addition of chemical substances
    • B01D19/0404Foam dispersion or prevention by addition of chemical substances characterised by the nature of the chemical substance
    • B01D19/0413Foam dispersion or prevention by addition of chemical substances characterised by the nature of the chemical substance compounds containing N-atoms
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/65Mixtures of anionic with cationic compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/0026Low foaming or foam regulating compositions
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/48Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial compositions
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/50Treatment of water, waste water, or sewage by addition or application of a germicide or by oligodynamic treatment
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2103/00Nature of the water, waste water, sewage or sludge to be treated
    • C02F2103/02Non-contaminated water, e.g. for industrial water supply
    • C02F2103/023Water in cooling circuits
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2103/00Nature of the water, waste water, sewage or sludge to be treated
    • C02F2103/26Nature of the water, waste water, sewage or sludge to be treated from the processing of plants or parts thereof
    • C02F2103/28Nature of the water, waste water, sewage or sludge to be treated from the processing of plants or parts thereof from the paper or cellulose industry
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2103/00Nature of the water, waste water, sewage or sludge to be treated
    • C02F2103/42Nature of the water, waste water, sewage or sludge to be treated from bathing facilities, e.g. swimming pools
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2303/00Specific treatment goals
    • C02F2303/04Disinfection
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2303/00Specific treatment goals
    • C02F2303/12Prevention of foaming
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2305/00Use of specific compounds during water treatment
    • C02F2305/04Surfactants, used as part of a formulation or alone
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/123Sulfonic acids or sulfuric acid esters; Salts thereof derived from carboxylic acids, e.g. sulfosuccinates
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/60Sulfonium or phosphonium compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/62Quaternary ammonium compounds

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • General Health & Medical Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Toxicology (AREA)
  • Organic Chemistry (AREA)
  • Dispersion Chemistry (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Environmental Sciences (AREA)
  • Dentistry (AREA)
  • Agronomy & Crop Science (AREA)
  • Zoology (AREA)
  • Epidemiology (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Description

WO 2008/049616 PCT/EP2007/009271 Controlled Foam Aqueous Quaternary Ammonium and Phosphonium Compositions This invention relates to a method for controlling foam formation in aqueous systems con taining biocidal quaternary ammonium and/or phosphonium compounds ("quats"). This in 5 vention also relates to low foam aqueous formulations comprising quaternary ammonium and/or phosphonium compounds and the use of said formulations compounds in a method for killing or inhibiting the growth of microorganisms, algae and fungi. Several quaternary ammonium and phosphonium compounds ("quats") exhibit marked biocidal 10 activity and, consequently, have been used as active ingredients in disinfectants, preservatives, or other compositions for killing or controlling the growth of microorganisms, such as bacteria or viruses, as well as algae and fungi for many years. However, since many of those quats have also surfactant properties, their use in aqueous systems is often impaired by intensive foaming even at low quat concentrations in the ppm range, which is particularly detrimental in appli 15 cations where aqueous systems are agitated while being exposed to the atmosphere, such as swimming pool or spa waters or waters in cooling towers. The problem to be solved by the present invention was to provide a method for the suppression of foaming in aqueous systems containing at least one biocidal quat. 20 According to the invention, the problem has been solved by the method of claim 1. Applicants have found that the addition of at least one anionic surfactant to an aqueous system containing at least one biocidal quaternary ammonium and/or phosphonium compound in an amount cor responding to a molar ratio of anionic surfactant to quaternary ammonium and/or phosphonium 25 compound of from 0.001 to 0.2 (i.e., 0.001:1 to 0.2:1), preferably from 0.001 to 0.09, substan tially reduces the volume and lifetime of foam formed during the use of the aqueous system. As anionic surfactants are known to decrease the biocidal efficacy of quaternary ammonium compounds, the observed foam reduction achieved by addition of anionic surfactants at much 30 less than a molar equivalency is important from the quat performance perspective. Since only small amounts of e.g. 0.1 or 0.02 molar equivalents of anionic surfactant are required, the com positions retain about 90 or 98 percent, respectively, of their active quat concentrations. In a more preferred embodiment, the molar ratio of anionic surfactant to quaternary ammonium 35 and/or phosphonium compound is from 0.001 to 0.05.
WO 2008/049616 PCT/EP2007/009271 -2 Preferably, the at least one quaternary ammonium and/or phosphonium compound is selected from (i) a compound having the formula [QR R2R3R 4 ] X (1), wherein Q is nitrogen or phosphor us, Rand R2 are independently unsubstituted or hydroxy-substituted linear or branched 5 Ci_4 alkyl; -(CH 2
CH
2 O)mCH 2
CH
2 OH, or -(CH 2
CH(CH
3 )O)mCH 2
CH(CH
3 )OH, where m in each molecule independently is an integer from 1 to 10;
R
3 is an optionally substituted benzyl, ethylbenzyl, naphthylmethyl, or linear or branched C6 22 alkyl group;
R
4 is an optionally substituted benzyl, ethylbenzyl, methylnaphthyl, or linear or branched 10 C 1 22 alkyl group or -R 5 (O)n(C 6
H
4
)R
6 , wherein n is 0 or 1;
R
5 is substituted or unsubstituted CIA alkanediyl or -(CH2)p-O-(CH2)q- wherein p and q independently are integers from 1 to 8;
R
6 is hydrogen or a substituted or unsubstituted, linear or branched C 1
-
1 2 alkyl group; and X- is a monovalent or one equivalent of a polyvalent anion; 15 (ii) a compound having the formula R' 9
R
2 0
R
2
R
22 Q+X~ (II), wherein Q is nitrogen or phosphorus, R19, R20, R , and R2 are independently linear, branched, cyclic or any combination thereof saturated or unsaturated hydrocarbyl groups, X- is a monovalent or one equivalent of a polyvalent anion, and the sum of the carbon atoms numbers of R' 9 , R20, R 2 1 and R ranges from 10 to 50; 20 (iii) a polymeric quaternary ammonium or phosphonium biocide; and (iv) a mixture of two or more quaternary compounds of any of (i) to (iii). More preferably, the quaternary ammonium and/or phosphonium compound has the formula
[QR'R
2
R
3
R
4 ]* X (I), wherein Q is as defined above, both R' and R 2 are Ci_4 alkyl, R 3 is a 25 linear or branched C- 22 alkyl, R 4 is benzyl or a linear or branched CI- 22 alkyl and X- is chloride. Still more preferably, the quaternary ammonium and/or phosphonium compound has the formula [QR'R 2
R
3
R
4 ]* X~ (I), wherein Q is as defined above, both R' and R 2 are methyl, R 3 is a 30 linear or branched C- 22 alkyl, R 4 is benzyl or a linear or branched C- 22 alkyl and X~ is chloride. Most preferably, Q is nitrogen. 35 Particularly preferred are ammonium and phosphonium compounds such as alkyldimethyl benzylammonium chloride or tributyl-tetradecylphosphonium chloride.
WO 2008/049616 PCT/EP2007/009271 -3 In another preferred embodiment, X- in formula (I) and/or (II) is selected from the group consisting of %CO3, HCO 3 and OH~. In still another preferred embodiment the at least one anionic surfactant is a sulfonate. 5 In another preferred embodiment the at least one anionic surfactant is a diester. In a particularly preferred embodiment, the at least one anionic surfactant is selected from the group consisting of diamyl sulfosuccinate, dihexyl sulfosuccinate, dioctyl sulfosuccinate, ditri 10 decyl sulfosuccinate, the potassium, sodium and calcium salts of any of the foregoing and any mixture of any of the foregoing sulfosuccinates and salts. In one most preferred embodiment, the at least one anionic surfactant is selected from the group consisting of dihexyl sulfosuccinate and the potassium, sodium and calcium salts thereof 15 sulfonate. In another most preferred embodiment, the at least one anionic surfactant is selected from the group consisting of dioctyl sulfosuccinate and the potassium, sodium and calcium salts thereof. 20 In still another most preferred embodiment, the at least one anionic surfactant is selected from the group consisting of diamyl sulfosuccinate and the potassium, sodium and calcium salts thereof. Of the above sulfosuccinate salts, the sodium salts are particularly preferred. 25 The above sulfonates have been observed to substantially reduce foaming while maintaining a high level of quat activity. Preferably, the aqueous system contains from 0.1 to 100 ppm, more preferably from 0.5 to 30 50 ppm, of the biocidal quaternary ammonium and/or phosphonium compound. Another object of the invention is a low foam formulation comprising at least one biocidal quaternary ammonium and/or phosphonium compound and at least one anionic surfactant, wherein the molar ratio of anionic surfactant(s) to quaternary ammonium and/or phosphonium 35 compound(s) is from 0.001 to 0.2, preferably from 0.001 to 0.09 and more preferably from 0.001 to 0.05.
WO 2008/049616 PCT/EP2007/009271 -4 Preferably, the low foam formulation comprises 5 to 80 wt.%, more preferably 10 to 50 wt.%, based on 100 wt.% total formulation, of the at least one biocidal quaternary ammonium and/or phosphonium compound. 5 The low foam formulations of the present invention are stable single phase clear solutions. Preferably the low foam formulation contains at least one performance additive such as a dye or perfume. 10 Still another object of the invention is a method for killing or inhibiting the growth of microorganisms, zooplankton, algae and/or fungi comprising applying the above formulations to an aqueous system or to a porous or hard surface. In a preferred embodiment the porous or hard surface is wood, metal or plastic. 15 In another preferred embodiment the formulation is used as a wood preservative. In still another preferred embodiment the formulation is used as a disinfectant or sanitizer for hard surfaces. 20 In yet another preferred embodiment the aqueous system is selected from the group consisting of cooling waters, waste waters, waters used on oil fields for injection, test or recovery purposes, recreational pool or spa waters, ballast water, and pulp or papermaking slurries. 25 Most preferably, the aqueous system is cooling water, ballast water or recreational pool or spa water. Particularly preferred is the application as algaecides in pool or spa waters. 30 Preferably, the aqueous system contains from 0.1 to 100 ppm, preferably from 0.5 to 50 ppm, of the biocidal quaternary ammonium and/or phosphonium compound. The invention is further illustrated by the following non-limiting examples. 35 Examples Method: Test solutions were prepared from the selected quaternary ammonium compounds and the selected anionic surfactants in 20 'C tap water (pH = 7-8, Total Hardness = 160-300 ppm as WO 2008/049616 PCT/EP2007/009271 -5 CaCO 3 and Total Alkalinity = 150-250 ppm as CaCO 3 ). 150 mL of each test solution was added to a 250 mL stoppered graduated mixing cylinder, the solution was agitated by inverting the cylinder ten times and the foam volume measured immediately after agitation and again after 30 seconds settling time. Also measured was the time for total collapse of the foam ("time 5 to no foam"). All quat concentrations in ppm or percent are on a weight basis and refer to the actual content of active ingredient, unless otherwise indicated. Example 1 (Reference Example) An alkyl (67% C 12 , 25% C 1 4 , 7% C 1 6 , 1% C 8 , 10, 18) dimethylbenzylammonium chloride 10 (ADBAC; Barquat* 50-65B, Lonza Inc., Allendale, NJ) was selected as a representative quaternary ammonium compound for foam evaluation. As shown in Table I below, ADBAC produced a substantial amount of foam, generating an initial foam volume of 25 mL and maintaining 10 mL of foam after 30 seconds. As a comparison, the foaming behavior of the polymeric quat poly[oxyethylene(dimethyliminio)ethylene(dimethyliminio)ethylene dichloride] 15 (WSCP; Buckman Laboratories International, Inc., Memphis, TN) was also tested. Example 2 The effect of the anionic surfactant sodium dioctyl sulfosuccinate (NaDOSS) on ADBAC foaming was determined as decribed above. The results are shown in Table I below. The 20 addition of only a 0.1 molar equivalent of NaDOSS relative to the active quat reduced the initial foam volumes by 85 percent from 25 mL to 4 mL. Even the application of only a 0.02 molar equivalent of NaDOSS resulted in merely 6 mL initial foam volume and complete foam loss within 10 seconds. 25 Example 3 The ability of NaDOSS to control foam at low concentrations of quaternary ammonium compounds, as they are frequently utilized in water treatment applications such as swimming pool algaecides, was tested at quat concentrations of 2 ppm using the methodology of Example 2. For comparison purposes one test was performed without addition of NaDOSS. The results 30 are shown in Table 1 below. It has been found that NaDOSS concentrations as low as 0.05 ppm can control foaming at 2 ppm quat concentration. Example 4 The alternative anionic surfactants sodium dihexyl sulfosuccinate (NaDHSS) and sodium ditri 35 decyl sulfosuccinate (NaDTSS) were also tested as foam reducing agents using the method ology of Example 2. The results are shown in Table 1 below. It has been found that NaDHSS concentrations as low as 1.1 ppm controlled foaming of 10 ppm quat (corresponding to a molar ratio of anionic surfactant to quat of 0.10) while concentrations as low as 0.2 ppm still showed a WO 2008/049616 PCT/EP2007/009271 -6 small effect. Similar results have been obtained with NaDTSS at concentrations of 1.7 ppm (corresponding to a molar ratio of anionic surfactant to quat of 0.10) and 0.4 ppm, respectively. NaDHSS was preferred as it produced clear solutions at all tested concentrations. 5 Table 1 Quat Sulfonate Foam Volume Example No. Sulfonate/Quat [mtl Time to No Type Amount Type Amount Molar Ratio Initial 30s Foam [s] [ppm] [ppm] 1 50-65B 10 - - 0 25 10 >30 1 WSCP 10 - - 0 0 0 <1 2 50-65B 10 NaDOSS 1.3 0.1 4 0 5 2 50-65B 10 NaDOSS 0.26 0.02 6 0 10 3 50-65B 2 - - 0 20 0 20 3 50-65B 2 NaDOSS 0.05 0.02 10 0 5 4 50-65B 10 NaDHSS 1.1 0.1 10 0 8 4 50-65B 10 NaDHSS 0.2 0.02 20 4 >30 4 50-65B 10 NaDTSS 1.7 0.1 10 0 4 4 50-65B 10 NaDTSS 0.4 0.02 20 2 >30 Example 5 As shown in the preceding examples, NaDOSS can be applied separately to quat-containing solutions to achieve the desired foam reduction. However, for practical reasons, in particular 10 ease of application, it is desirable to provide single formulations (concentrates) containing the quats and the anionic surfactants in an optimized molar ratio. Therefore the phase stability of two formulations containing Barquat* 50-65B and NaDOSS was tested. The results are shown in Table 2 below. 15 Table 2 NaDOSS/Quat Molar Ratio Quat Content [%] NaDOSS Content [%] Appearance 0.02 49.2 1.2 Single phase, clear 0.10 46.1 5.8 Single phase, clear It has been found that clear phase-stable formulations containing NaDOSS and ADBAC in molar ratios of 0.02 and 0.10 can be prepared. Test solutions with 10 ppm quat were prepared from these formulations and showed essentially the same foaming behavior as those of 20 Example 2.
WO 2008/049616 PCT/EP2007/009271 -7 Example 6 Sodium dioctyl sulfosuccinate (NaDOSS) and sodium dihexyl sulfosuccinate (NaDHSS) were tested in a dynamic recirculation foam test designed to simulate cooling applications. The dynamic foam test consisted of recirculating a 1.5 liter water sample through a large graduated 5 cylinder at a flow rate of 5.7 liter/min (1.5 GPM). The water conditions were: total hardness (as CaCO 3 ) 280 ppm, total alkalinity (as CaCO 3 ) 164 ppm, temperature 22 C, and pH = 7.3. Master solutions of the test formulations were added as necessary to achieve the reported concentrations. The results are compiled in Table 3 below. 10 Table 3 Sample Stabilized Foam Height After 5 Minutes (cm) LF 7.25-8.0 LF + 0.02 mol NaDOSS 4.0 LF + 0.02 mol NaDHSS 6.0 Both tested compounds significantly reduced the foaming properties of 90 ppm active dioctyldi methylammonium chloride (Bardac* LF 18, Lonza Inc.). As shown in Table 3, the addition of NaDOSS at a molar ratio (sulfosuccinate/Bardac* LF 18) of 0.02 provided a 50% foam 15 reduction, from 8 cm to 4 cm, while addition of NaDHSS at the same molar ratio provided a 25% foam reduction. Example 7 The phase stability of two formulations containing Bardac* LF 18 and NaDOSS were tested. 20 As shown in Table 4 below, formulations containing NaDOSS at molar ratios of 0.02 and 0.05 are compatible, providing clear, single phase solutions. Table 4 NaDOSS/Quat Molar Ratio Quat Content [%] NaDOSS Content [%] Appearance 0.02 51.0 1.5 Single phase, clear 0.05 50.0 3.6 Single phase, clear

Claims (21)

1. A method for controlling foam formation in an aqueous system containing at least one biocidal quaternary ammonium and/or phosphonium compound, said method comprising 5 the addition of at least one anionic surfactant in a molar ratio of anionic surfactant to quaternary ammonium and/or phosphonium compound of from 0.001 to 0.2, preferably 0.001 to 0.09, to said aqueous system.
2. The method of Claim 1, wherein the molar ratio of anionic surfactant to quaternary 10 ammonium and/or phosphonium compound is from 0.001 to 0.05.
3. The method of Claim I or 2, wherein the at least one quaternary ammonium and/or phosphonium compound is selected from (i) a compound having the formula [QR R2R3R4]* X~ (I), wherein 15 Q is nitrogen or phosphorus, preferably nitrogen; R'and R 2 are independently unsubstituted or hydroxy-substituted linear or branched CI_4 alkyl; -(CH 2 CH 2 0)mCH 2 CH 2 OH, or -(CH 2 CH(CH 3 )O)mCH 2 CH(CH 3 )OH, where m in each molecule independently is an integer from I to 10; R 3 is an optionally substituted benzyl, ethylbenzyl, naphthylmethyl, or linear or 20 branched C6 22 alkyl; R 4 is an optionally substituted benzyl, ethylbenzyl, methylnaphthyl, or linear or branched C 1 22 alkyl or -R 5 (O)n(C 6 H 4 )R 6 , wherein n is 0 or 1; R 5 is substituted or unsubstituted CIA alkanediyl or -(CH2)p-O-(CH2)q- wherein p and q independently are integers from 1 to 8; 25 R 6 is hydrogen or a substituted or unsubstituted, linear or branched CI 12 alkyl; and X is a monovalent or one equivalent of a polyvalent anion; (ii) a compound having the formula R I RRI R Q*X~ (II), wherein Q is as defined above, R' 9 , R 20 , R , and R 2 are independently linear, branched, cyclic or any combination 30 thereof saturated or unsaturated hydrocarbyl groups, X is a monovalent or one equivalent of a polyvalent anion, 19 20 and the sum of the carbon atoms numbers of R'9, R , R 2 ' and R 2 ranges from 10 to 50; (iii) a polymeric quaternary ammonium or phosphonium biocide; and 35 (iv) a mixture of two or more quaternary compounds of any of (i) to (iii). WO 2008/049616 PCT/EP2007/009271 -9
4. The method of Claim 3, wherein the quaternary compound has the formula [QR R 2 R 3 R 4 ]+ X-, Q is as defined in Claim 3, both R' and R 2 are CI_4 alkyl, R 3 is a linear or branched C,- 22 alkyl, R 4 is benzyl or a linear or branched C1- 22 alkyl and X- is chloride.
5 5. The method of Claim 3 or 4, wherein X is selected from the group consisting of M2CO, HCO 3 and OH_.
6. The method of any of Claims 1 to 5, wherein the at least one anionic surfactant is a sulfonate. 10
7. The method of any of Claims I to 6, wherein the at least one anionic surfactant is a diester.
8. The method of Claims 6 and 7, wherein the at least one anionic surfactant is selected from 15 the group consisting of diamyl sulfosuccinate, dihexyl sulfosuccinate, dioctyl sulfo succinate, ditridecyl sulfosuccinate, the potassium, sodium and calcium salts of any of the foregoing, and any mixture of any of the foregoing sulfosuccinates and salts.
9. The method of Claim 8, wherein the at least one anionic surfactant is selected from the 20 group consisting of dihexyl sulfosuccinate and the potassium, sodium and calcium salts thereof.
10. The method of Claim 8, wherein the at least one anionic surfactant is selected from the group consisting of dioctyl sulfosuccinate and the potassium, sodium and calcium salts 25 thereof.
11. The method of any of Claims I to 10, wherein the aqueous system contains from 0.1 to 100 ppm, preferably from 0.5 to 50 ppm, of the biocidal quaternary ammonium and/or phosphonium compound. 30
12. A single-phase liquid low foam formulation comprising at least one biocidal quaternary ammonium compound and at least one anionic surfactant, wherein the molar ratio of anionic surfactant(s) to quaternary ammonium compound(s) is from 0.001 to 0.2, prefera bly from 0.001 to 0.09 and more preferably from 0.001 to 0.05. 35
13. The formulation of Claim 12 comprising 5 to 80 wt.%, preferably 10 to 50 wt.%, based on 100 wt.% total formulation, of the at least one biocidal quaternary ammonium and/or phosphonium compound. WO 2008/049616 PCT/EP2007/009271 - 10
14. The formulation of Claim 12 or 13 containing a dye or perfume or other performance additive.
15. A method for killing or inhibiting the growth of microorganisms, algae and/or fungi, said 5 method comprising applying the formulation of any of Claims 12 to 14 to an aqueous system or to a porous or hard surface.
16. The method of Claim 15, wherein the porous or hard surface is wood, metal or plastic. 10
17. The method of Claim 16, wherein the formulation is used as a wood preservative.
18. The method of Claim 15, wherein the formulation is used as a disinfectant or sanitizer for hard surfaces. 15
19. The method of Claim 15, wherein the aqueous system is selected from the group con sisting of cooling waters, waste waters, waters used on oil fields for injection, test or recovery purposes, recreational pool or spa waters, ballast water, and pulp or paper making slurries.
20 20. The method of Claim 19, wherein the aqueous system is cooling water, ballast water or recreational pool or spa water.
21. The method of Claim 19 or 20, wherein the aqueous system contains from 0.1 to 100 ppm, preferably from 0.5 to 50 ppm, of the biocidal quaternary ammonium and/or 25 phosphonium compound.
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