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Publication numberUS3689421 A
Publication typeGrant
Publication dateSep 5, 1972
Filing dateApr 9, 1971
Priority dateApr 9, 1971
Publication numberUS 3689421 A, US 3689421A, US-A-3689421, US3689421 A, US3689421A
InventorsBriggs Benjamin R
Original AssigneePurex Corp Ltd
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Household hypochlorite bleach with stable latex opacifier
US 3689421 A
Abstract  available in
Previous page
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Claims  available in
Description  (OCR text may contain errors)

United States Patent O 3,689,421 HOUSEHOLD HYPOCHLORITE BLEACH WITH STABLE LATEX OPACIFIER Benjamin R. Briggs, Los Alamitos, Calif., assignor to Purex Corporation, Ltd., Lakewood, Calif.

No Drawing. Continuation-impart of abandoned application Ser. No. 714,449, Mar. 20, 1968. This application Apr. 9, 1971, Ser. No. 132,805

Int. Cl. C01b 11/06 US. Cl. 252-95 11 Claims ABSTRACT OF THE DISCLOSURE Liquid household bleach having visual opacity is provided by the incorporation into the bleach of a particularly prepared styrene-vinyl acid copolymer latex which is highly resistant to deterioration in the bleach and which enables maintenance of useful available chlorine levels over extended periods of time. The latex is prepared by introduction of styrene monomer into a preformed aqueous solution of the vinyl acid and a noncationic surfactant.

REFERENCE TO RELATED APPLICATION This application is a continuation-in-part of my copending application Ser. No. 714,449, filed Mar. 20, 1968, and now abandoned.

BACKGROUND OF THE INVENTION (1) Field of the invention This invention has to do with household liquid bleach. The invention is particularly concerned with household bleach of the sort ordinarily added to detergent containing water for the purpose of whitening fabrics being washed. For the most part, liquid household bleach cornprises a highly alkaline solution of sodium hypochlorite usually having an appreciable available chlorine content and a pH of or more. More recently, other sources of hypochlorite ion have been developed, primarily for solid bleaches sold in tablet form. Such materials e.g., trichlorocyanurates may, however, be sold as liquid bleaches and may take advantage of the present invention.

Liquid household bleaches now on the market are watery-appearing, slightly tinted fluids. It has been found that consumer reaction is less favorable to watery products than to equally effective products which have a degree of body giving them an appearance of greater substance.

(2) Prior art In the liquid detergent field, finely particulate resins are added to the aqueous or alcoholic detergent solution to impart visual opacity and pleasing body and coloration.

Attempts to opacify liquid household bleach have not been successful in the past because of instability of the opacifying resin latex in the harsh environment presented by liquid bleach. Great alkalinity, combined with the presence of chlorine ion appears to destroy the latex through decomposition of the resin or of the emulsifying agents. Thus, even resins having known stability to chlorine-containing solutions, such as polystyrene, have not proved useful as opacifiers, because of the inability of the polymer to remain dispersed in the bleach solution for a period of time equal to storage, shipping and shelf time, expectably encountered in the normal marketing of bleach. Concomitantly, the chlorine in reacting reduces the available chlorine in the bleach over time to an unacceptably low level for bleaching utility.

In US. Pat. 3,393,153, a fluorescent bleach is taught to require the presence of a stabilizer for the fluorescent agent. Suitable stabilizers are inorganic or organic and these are taught to opacity the bleach, the effect of such stabilizers on available chlorine levels is not noted in the patent.

SUMMARY OF THE INVENTION It is a major objective of the present invention to provide liquid household bleach stably opacified for a more substantial and attractive appearance, and which retains its available chlorine at an acceptable level over time.

Accordingly, there is provided a liquid household bleach comprising an aqueous, highly alkaline solution containing hypochlorite ion and a latex of finely particulate synthetic organic polymer consisting essentially of a styrene monomer which has been emulsion polymerized at an elevated temperature following addition to an aqueous solution of a vinyl acid and a noncationic surfactant. The polymer typically contains copolymerized from 65 to 98 parts of the styrene monomer and 2 to 35 and preferably 8 to 12 parts of vinyl acid per 100 parts of the polymer, by weight. In general, the polymer is of opacifying size range, e.g. 0.1 to 2 microns in average particle size and is present in amounts between 0.005 and 5 percent by weight. The styrene component of the polymer may be styrene per se, i.e. vinyl benzene, or other styrene having up to 12 carbon atoms and possibly monohalogen substituted as in chlorostyrene. The vinyl acid component of the polymer may be an a, 13 ethylenically unsaturated monocarboxylic acid containing from 3 to 4 carbon atoms, i.e. acrylic or methacrylic acid. From 0.5 to 25 parts by weight of a hydrophilic acrylic acid derivative comonomer may replace a corresponding portion of the styrene component in the polymer, primarily to increase particle size. These comonomers may be the hydroxyesters, ethers, amides and cyano derivatives of acrylic and methacrylic acids. Preferably from 5 to 10 parts by weight of the hydroxyalkyl derivative of methacrylic acid in which the alkyl group contains from 1 to 4 carbon atoms is used in replacement of a corresponding portion of the styrene component of the polymer.

The liquid household bleach is, except for the presence of the specified opacifier, typical of commercially available products and accordingly will have a pH of 10 or more and a hypochlorite ion concentration of 1 to 10 percent by weight, generally derived from sodium hypochlorite, to have an initial available chlorine above about 65 gms./ liter.

A noncationic surfactant is used to form the polymer latex. Typical surfactants are anionic materials and nonionic polyalkylene oxide derivatives of alkylene glycols or phenols.

DESCRIPTION OF THE PREFERRED EMBODIMENTS The liquid household bleach opacified in accordance with this invention may be any hypochlorite ion containing solution containing suflicient free alkali to have a pH of 10 and preferably 11.5 and higher, typically from 0.1 to 1.0% by weight free alkali. Percent concentrations of hypochlorite ion will range between 1 and 10 percent by weight with a practical minimum being 2.5%. Most bleaches fall between 3 and 7% hypochlorite ion, and this concentration is most suited to use of the invention. As mentioned above various bleaching agents including the heterocyclic N-chlorimides such as the following are useful herein:

Trichlorocyanuric acid, dichlorocyanuratic acid and salts thereof such as the alkali metal salts, e.g. sodium and potassium tri-acid dichlorocyanurates. Other imides are hypochlorite ion generating also in aqueous solution and may be used, e.g. N-chlorosuccinimide, N-chloromalonimide, N-chlorphthalimide and N-chloronaphthalimide.

Other materials are the hydantoins, e.g. the 1,3-dichloro-5, S-dimethyl hydantoin, N-monochloro-C,C-dimethyl-hydantoin, methylene bis (N-chloro-C, C-dimethylhydantoin), l,3-dichloro-S-methyl--isobutyldimethylhydantoin, 1,3-dichloro-5-methyl 5 ethylhydantoin, 1,3-dichloro-5- methyl-Sn-amylhydantoin and the like as well as trichloromelamine. Preferred sources of hypochlorite ion are the water soluble inorganic salts such as lithium, calcium, potassium and particularly sodium hypochlorite.

The opacifying polymer is a particulate form of a styrene copolymer formed in a critical manner. It has been found that most polymer latices prepared from a styrene and a vinyl acid within the proportions herein described and with or 'without a termonomer such as a vinyl acid ester are not stable in highly alkaline, liquid bleach compositions. Surprisingly the same proportions of monomers provide vastly different opacifying benefits depending on the polymerization technique employed. To get useful latices of particulate styrene copolymer for opacifying bleach it has been found essential to first form a solution of the vinyl acid monomer in water and the noncationic surfactant prior to adding the styrene monomer to the reaction vessel. In this manner a latex having styrene copolymer finely dispersed therethrough is obtained which is stable for long periods even at elevated temperatures in liquid houshold bleach and which does not so react with the bleach as to deplete available chlorine to unacceptable levels during normal shelf life of the bleach.

As the polymer components there may be employed styrene per se or vinyl benzene or a substituted styrene such as vinyl toluene or butyl styrene, i.e. alkyl substituted styrenes in which the alkyl groups contain from 1 to 4 carbon atoms such that the styrene monomer contains from 8 to 12 carbon atoms, inclusive. Or the styrene monomer may be monohalogen ring substituted such as chlorostyrene or bromostyrene. The vinyl acid component may be described generically as a water soluble a, B ethylenically unsaturated monocarboxylic acid. Typically such acids will contain from 3 to 5 carbon atoms, e.g. acrylic, crotonic, itaconic or methacrylic acids. The proportions of styrene monomer and vinyl acid monomer are from 65 to 98 parts styrene and conversely from 2 to 35 parts of the vinyl acid per 100 parts by weight of the copolymer.

Polymerization is carried out as hereinafter described to provide polymer particles ranging in size between 0.5 and 2 microns. To achieve this size range, particularly at the higher end thereof, it is often desirable to incorporate a third monomer in the polymer. This termonomer will be a hydrophilic acrylic monomer such as a derivative of methacrylic or acrylic acid and free of carboxyl groups. Thus, such derivatives as the ester, hydroxyester, ether, amide or cyano derivatives of acrylic or methacrylic acids may be used in amounts of from 0.5 to 25 parts by Weight and preferably between 5 and parts by weight, in substitution for an equal weight amount of the styrene monomer, per 100 parts of the final opacifying terpolymer. Specific termonomers of choice include the hydroxyalkyl esters of methacrylic acid in which the alkyl group contains from 1 to 4 carbon atoms and particularly hydroxyethyl and hydroxypropyl methacrylate, and acrylamide, methacrylamide, acrylonitrile and methyl vinyl ether.

The monomers just described are emulsion polymerized using conventional catalysts, oxidizers or reducers, tem-- peratures and pressures but with the critical step of first dissolving the water soluble vinyl acid in water, suitably with the emulsifying surfactant, prior to addition of the styrene. If used, the hydrophilic vinyl termonomer should also be predissolved in water prior to introduction of styrene into the reaction vessel. Apart from the just-mentioned sequence of reactant introduction, the preparation of the polymers useful as opacifiers herein is carried out as for any other exothermic emulsion polymerization. Thus an aqueous solution of a suitable surfactant is mixed with the water soluble vinyl acid. Thereafter the water insoluble styrene reactant is mixed in and agitated until emulsified as the oil phase. The emulsion is then maintained at an elevated temperature through exothermic and/or added heat in admixture with a suitable catalyst, e.g. and preferably water soluble persulfates such as ammonium and sodium and potassium persulfate and peroxides, e.g. hydrogen peroxide; and also catalysts such as t-butyl perbenzoate and t-butyl hydroperoxide, as well as other oil soluble materials such as bisazobutyronitrile and cumene hydroperoxide. Following reaction for the required period and at temperatures between F. and boiling the reaction mixture is cooled and neutralized with alkali. The latex may be spray or otherwise dried without loss of dispersibility or stability in liquid household bleach.

As noted, polymers prepared using conventional procedures and from the same reactants and proportions are not stable in liquid household bleach and rapidly deteriorate in particle size and appear to disintegrate or react with the bleach to deplete available chlorine levels. While not wishing to be bound to any particular theory concerning the operation of the invention it is believed that the unusual resistance of the presently disclosed compositions to deterioration in bleach may be attributable to the favoring of reaction of the vinyl acid first in the reactor, followed relatively by the polymerization of the styrene monomer, resulting in a relative styrene richness at the surface of the obtained polymer beads, and a relative vinyl acid richness at the core of the beads. Styrene homopolymer is not satisfactory, of course, as a bleach opacifier, because it is not capable of stable dispersion in the bleach solution, since it lacks polarity. Suitable surfactants for effecting emulsion polymerization as described and/or for suspending the finely particulate polymer in bleach are the noncationic types, i.e. anionic, nonionic or amphoteric. Various of these surfactants will show greater or less tolerance for the harsh environment of liquid household bleach, depending on the concentration and pH thereof.

Among suitable surfactants are anionic aromatic compounds, e.g. water-soluble higher alkyl aryl sulfonates particularly those having from 8 to about 15 carbon atoms in the alkyl group. It is preferred to use the higher alkyl benzene sulfonates, although other mononuclear aryl nuclei, such as toluene, xylene, or phenol, may be used also. The higher alkyl substituent on the aromatic nucleus may be branched or straight-chained in structure, examples of such group being nonyl, dodecyl and pentadecyl groups derived from polymers of lower monoolefins, decyl, keryl, and the like.

Illustrative of suitable aliphatic anionic compounds are the normal and secondary higher alkyl sulfates, particularly those having about 8 to 15 carbons in the fatty alcohol residue, such as lauryl (or coconut fatty alcohol) sulfate. Other suitable members of this class are the sulfuric acid esters of polyhydric alcohols incompletely esterified with higher fatty acids; the oleic acid ester of isethionic acid; the higher fatty acid (e.g. coconut) ethanolamide sulfates; the higher fatty acid amides of amino alkyl sulfonic acids, e.g. lauric acid amide of taurine; and the like.

These sulfates and sulfonates are used in the form of their water-soluble salts, such as the alkali metal and nitrogen-containing, e.g. lower alkylolamine, salts. Examples are the sodium, potassium, ammonium, isopropanolamine, monoand tri-ethanolamine salts of said higher alkyl benzene sulfonate, higher alkyl sulfate and the like.

Typical specific examples are:

The sodium salt of a sulfate ester of an alkylphenoxypoly (ethyleneoxy) ethanol, the ammonium salt of this sulfate ester, sodium methyl oleyl taurate, sodium alkyl naphthalene sulfonate, alkyl acyl sodium sulfonate, sodium tetraphydronaphthalene sulfonate, sodium alkyl aryl sulfonate, alkyl amido sulfate, cocomonoglyceride sulfate, dodecylbenzene sodium sulfonate, dodecylbenzene sulfonic acid, tridecylbenzene sodium sulfonate, fatty alcohol sodium sulfate, sodium dodecyl diphenyl oxide disulfonate, sulfonated castor oil, polyethoxyalkyl phenol sulfonate triethanolamine salts, sodium triethanolamine alkyl aryl sulfonate, magnesium lauryl sulfate, potassium lauryl sulfate, sodium lauryl ether sulfate, ammonium lauryl ether sulfate, sodium tallow sulfate, dodecylbenzene sodium sulfonate, oleyl methyl tauride, ammonium lauryl sulfate, amide sulfonate, and the like.

In general, suitable nonionic surfactants include those such as produced by the introduction of alkylene oxide group into an organic hydrophobic compound or group having an aliphatic or aromatic structure. The hydrophobic organic group generally contains at least 8 carbon atoms and up to about 30 carbon atoms. Condensed with the hydrophobic group are at least and preferably up to about 50 alkylene oxide groups. It is preferred to use the polyoxyethylene condensates derived from ethylene oxide. It is preferred to use the polyalkylene oxide condensates of alkyl phenol, such as the polyoxyethylene ethers or alkyl phenols having an alkyl group of at least about six, and usually about 8 to 12 carbons, and preferably 8 to 9 carbon atoms, and an ethylene oxide ratio (No. of moles per phenol) of about 7.5, 8.5, 11.5 or 20, though the number of ethylene oxide groups will be usually from about 8 to 40. The alkyl substituent on the aromatic nucleus may be di-isobutylene, diamyl, polymerized propylene, dimerized C -C olefin, and the like.

Further suitable nonionics are the polyoxyalkylene esters of organic acids, such as the higher fatty acids, rosin acids, tall oil acids, or acids from the oxidation of petroleum, et cetera. These polyglycol esters will contain usually from about 12 to about 30 moles of ethylene oxide or its equivalent and about 8 to 22 carbons in the acyl group. Suitable products are refined tall oil condensed with 16 or 20 ethylene oxide groups, or similar polyglycol esters of lauric, stearic, oleic acids, etc.

Additional nonionic agents are the polyalkylene oxide condensates with higher fatty acid amides, such as the higher fatty acid primary amides, monoand di-ethanolamides. Suitable agents are coconut fatty acid amide condensed with about to 50 moles of ethylene oxide. The fatty acyl group will have similarly about 8 to 22 carbons, and usually about 10 to 18 carbon atoms, in such products. The corresponding sulfonamides may be used also if desired.

Other suitable polyethyl nonionics are the polyalkylene oxide ethers of high aliphatic alcohols. Suitable fatty alcohols having a hydrophobic character, preferably 8 to 22 carbons, are lauryl, myristyl, cetyl, stearyl and oleyl alcohols which may be condensed with an appropriate amount of ethylene oxide, such as at least about 6, and preferably about 10 to 30 moles. A typical product is oleyl alcohol condensed with about 12, or moles of ethylene oxide. The corresponding higher alkyl mercaptans or thio-alcohols condensed with ethylene oxide are suitable in the present invention also. The water-soluble polyoxyethylene condensates with hydrophobic polyoxypropylene glycols may be employed also, e.g. the ethylene oxide condensates with condensates of propylene oxide and propylene glycol.

Further suitable nonionic materials are the higher fatty acid alkanolamides, such as the monoethanolamides, diethauolamides and isopropanolamides wherein the acyl radical has about 10 to 14 carbon atoms and amine oxides. Examples are coconut (or equivalent lauric), capric and myristic diethanolamide, monoethanolamide and isopropanolamide, dodecyl dimethyl amine oxide and dimethyl acetoxyalkylamine oxide where alkyl is C11"C14- Generally, these surfactants comprise from 0.05 to 10 percent by weight, and preferably from 0.5 to 3% of the reaction mixture and the latex added to the liquid house hold bleach.

The invention is illustrated by the following examples, in which all parts are by weight.

6 EXAMPLE 1 (A) Polymer preparation One part of dioctyl ester of sodium sulfosuccinic acid was dissolved in 750 parts of water. There was added and dissolved 50 parts of methacrylic acid and 10 parts of hydroxyethyl methacrylate. Following achieving complete solution, 500 parts of vinyl toluene was added. Heat was applied to raise the mixture temperature to F. One-half part sodium persulfate (initiator) and one-tenth part sodium formaldehyde sulfoxylate (reducing agent) were added. Temperature increased to 200 F. Thereafter reaction was completed and the reaction mixture cooled, neutralized with potassium hydroxide and filtered. Polymer particles were in the range of 0.5 to 2 microns in particle size. The product may be spray dried for subsequent incorporation into dry bleach products.

(B) Liquid bleach opacification One part of the latex obtained in A was mixed with 100 parts of a 5% aqueous solution of sodium hypochlorite having a pH of 11.5 to opacify the same. After 3 months at 70 F. the bleach was still opacified.

CONTROL I Example 1 was duplicated but the methacrylic acid was mixed first with styrene and then added to the aqueous surfactant solution, followed by heating to polymerize. In part B, the emulsion which had similar size particles and the same milky appearance prior to addition to the bleach as the example emulsion, showed immediate physical deterioration and quickly demulsified and settled as a fiocculated mass in the holding vessel.

EXAMPLE 2 (A) One part of the dioctyl ester of sodium sulfosuccinic acid was dissolved in 750 parts of water. There was added 50 parts of acrylic acid and 50 parts of methacrylamide and dissolved. Fifty parts of styrene were then added and emulsified with heating to F. and addition of 1 part of ammonium persulfate and one part sodium bisulfite. On rising of the temperature to -150 F. an additional 450 parts of styrene is added over a two hour period, with the temperature held by cooling at -170 F., followed by cooling to room temperature, neutralization and filter- (B) The product of A stably opacifies liquid household bleach.

EXAMPLE 3 Parts A and B of Example 1 are duplicated using butyl styrene for vinyl toluene. A stable opacified bleach is obtained.

EXAMPLE 4 Example 1 is duplicated but omitting addition of the hydroxyethyl methacrylate. A fine latex is obtained which is useful in opacifying bleach. Increased quantities of the latex, relative to those used in Example 1 are required to obtain equivalent opacity to Example 1.

CONTROL II Example 1 was duplicated but reducing the amount of methacrylic acid to 10 parts (0.5%) well below the minimum required herein. The latex obtained was stable for only two weeks in the test bleach solution.

EXAMPLE 5 0.2 part of dioctyl ester of sodium sulfosuccinic acid (Aerosol OT) was dissolved in 56.5 parts of soft water. There was added and dissolved 3.9 parts of methacrylic acid and 4.6 parts of vinyl sulfonate. Following complete solution of these monomers, 34.6 parts of styrene was added. The reaction mixture was heated to 120 F. 0.22 part of sodium persulfate as initiator and 0.08 part of sodium formaldehyde sulforalate (Formopan) were added.

Temperature rose to 190-200 F. Thereafter the reaction was completed, the reaction mixture cooled, neutralized with potassium hydroxide and filtered. Polymer particles were in the range of 0.1 to 2.0 microns.

EXAMPLE 6 A series of compositions were prepared to compare the product of Example in bleach with a commercial copolymer used for opacifying bleach (Mortons 13-290) Control III, with an unopacified bleach, Control IV in terms of stability of bleach over time at an elevated temperature.

Control III comprised 2970 grns. of Purex production bleach and 30 gms. of Mortons E-290 copolymer (described above). Control IV comprised 3000 gms. of Purex production bleach. Example 6 comprised 2970 grns. of Purex production bleach and 30 gms. of the copolymer prepared in Example 5. One drop of antifoam was added to each mixture.

The mixtures were divided into three portions of 1000 gms. each. The mixtures containing opacifier (Control III and Example 6) were placed in clear bottles, while the unopacified bleach (Control IV) was placed in an opaque blue plastic bleach bottle. Available chlorine tests were run on each sample with these results.

INITIAL AVAILABLE CHLORINE The samples were stored variously at room temperature (RT) and at 90 F., and their available chlorine measured after one week.

1 WEEK STORAGE Test condition Control III: Avail. Cl (gms./liter) RT 66.2

Control IV:

Example 6:


Control IV:

Example 6:


Control IV:

Example 6:

8 AFTER FOUR MONTHS STORAGE Control III (IE-290): Avail. Cl (gms./liter) 1 Trace Control IV: 2

90 43.9 Example 6:

CONTROL V A copolymer of styrene and methacrylic acid prepared in latex form as in Example 1 but to have a particle size of 25 microns and a molecular weight of 2,000,000 is added to bleach. The copolymer immediately settles. This was attributable to too great particle size in the latex.

I claim:

1. Liquid household bleach having visual opacity and consisting essentially of an aqueous, highly alkaline solution containing 1 to 10% by weight hypochlorite ion and from 0.05 to 5% by weight of a latex of finely particulate synthetic organic polymer consisting essentially of a styrene monomer containing from 8 to 12 carbon atoms which has been emulsion polymerized at an elevated temperature following addition to an aqueous solution of an 8 ethylenically unsaturated monocarboxylic acid containing from 3 to 5 carbon atoms and a noncationic surfactant, said polymer containing copolymerized per parts by weight from '65 to 98 parts of the styrene monomer and from 2 to 35 parts by weight of the vinyl acid and having a particle size from 0.1 to 2 microns.

2. Liquid household bleach according to claim 1 in which said styrene monomer is monohalogen ring substituted.

3. Liquid household bleach according to claim 4 in which said styrene monomer is vinyl benzene.

4. Liquid household bleach according to claim 1 in which said vinyl acid is acrylic acid.

5. Liquid household bleach according to claim 1 in which said vinyl acid is methacrylic acid.

6. Liquid household bleach according to claim 10 including sodium hypochlorite as source of hypochlorite 1011.

7. Liquid household bleach according to claim 6 in which said bleach has a pH above 10.

8. Liquid household bleach according to claim 1 including :also from 0.5 to 25 parts of a hydrophilic acrylic comonomer selected from the hydroxyester, ether, amide and cyano derivatives of methacrylic and acrylic acids in substitution of corresponding portion of the styrene monomer.

9. Liquid household bleach according to claim 8 in which the comonomer is present in an amount between 5 and 10 parts and is an hydroxyalkyl ester of methacrylic acid in which the alkyl group contains from 1 to 4 carbon atoms and said vinyl acid is present in an amount between 8 and 12 parts per 100 parts of said polymer.

10. Liquid household bleach composition having visual opacity and adequate levels of available chlorine for four months or more consisting essentially of an aqueous highly alkaline solution containing about 5% by weight hypochlorite ion and about 1% by weight of a latex of a finely particulate synthetic organic terpolymer consisting essentially of styrene polymerized in a previously prepared aqueous mutual solution of an acrylic acid having 3 or 4 carbon atoms, an hydroxyalkyl ester of acrylic acid ormethacrylic acid and an anionic surfactant, said terpolymer containing copolymerized per 100 parts by weight about 10 parts of said acid, about 10 parts of said ester and about 80 parts styrene.

11. Method of preparing a stable, visually opacified liquid bleach composition having adequate levels of available chlorine for four months or more by suspension in the bleach of finely particulate styrene containing polymer which includes forming latex of a polymer consisting essentially of 65 to 98 parts of a styrene monomer containing 8 to 12 carbon atoms inclusive and 2 to 35 parts of acrylic or methacrylic acid by adding the styrene as a monomer to an aqueous solution acid containing a surfac- References Cited UNITED STATES PATENTS 3,244,658 4/1966 Grosser et al 26029.6 E 3,282,876 11/1966 Williams et a1. 260-296 E 3,297,619 1/1967 Bluhm et al 260-296 E 3,393,153 7/1968 Zimmerer et a1 252-187 MAYER WEINBLA'IT, Primary Examiner I. GLUCK, Assistant Examiner U.S. Cl. X.R.

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US4457855 *Jun 8, 1981Jul 3, 1984The Clorox CompanyStable hypochlorite solution suspendable dyes
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US4929383 *Oct 20, 1986May 29, 1990The Clorox CompanyStable emulstified bleaching compositions
US4931207 *Jul 18, 1988Jun 5, 1990The Clorox CompanyBleaching and bluing composition and method
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US5256328 *Dec 16, 1992Oct 26, 1993Eastman Kodak CompanyLiquid toilet bowl cleaner and sanitizer containing halogen donating nanoparticles
US20070287651 *Jun 8, 2007Dec 13, 2007The Procter & Gamble CompanyBleaching compositions
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U.S. Classification252/187.26, 252/187.34, 510/303, 8/108.1, 252/187.25, 423/473, 252/187.33, 510/416, 252/187.29, 510/370, 524/401
International ClassificationC11D3/37, C11D3/395
Cooperative ClassificationC11D3/3951, C11D3/3956, C11D3/3765
European ClassificationC11D3/395B, C11D3/395H, C11D3/37C6F
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Effective date: 19820428
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Effective date: 19820813