US3915902A - Cleaning compositions - Google Patents

Cleaning compositions Download PDF

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Publication number
US3915902A
US3915902A US392647A US39264773A US3915902A US 3915902 A US3915902 A US 3915902A US 392647 A US392647 A US 392647A US 39264773 A US39264773 A US 39264773A US 3915902 A US3915902 A US 3915902A
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Prior art keywords
sodium
compositions
water
weight
glycol
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US392647A
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Selwyn J Ancel
James O Gladish
Floyd L Mickelson
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SYSTEMS GENERAL Inc
Chemtrust Ind Corp
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Chemtrust Ind Corp
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Application filed by Chemtrust Ind Corp filed Critical Chemtrust Ind Corp
Priority to US392647A priority Critical patent/US3915902A/en
Priority to GB3661774A priority patent/GB1438447A/en
Priority to DE2440608A priority patent/DE2440608A1/en
Priority to FR7429091A priority patent/FR2242461B3/fr
Priority to IT26650/74A priority patent/IT1020225B/en
Priority to JP49098808A priority patent/JPS5072905A/ja
Publication of US3915902A publication Critical patent/US3915902A/en
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Assigned to KEM MANUFACTURING CORPORATION, A GEORGIA CORPORATION reassignment KEM MANUFACTURING CORPORATION, A GEORGIA CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST. (SEE RECORD FOR DETAILS) Assignors: FIRST NATIONAL BANK OF CHICAGO, THE, A NATIONAL BANKING ASSOCIATION
Assigned to SYSTEMS GENERAL CORPORATION reassignment SYSTEMS GENERAL CORPORATION CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). EFFECTIVE JAN. 6, 1987 Assignors: KEM ACQUISITION, INC.
Assigned to FIRST NATIONAL BANK OF CHICAGO reassignment FIRST NATIONAL BANK OF CHICAGO Assignors: CHEMTRUST INDUSTRIES CORPORATION OF CALIFORNIA, A CA CORP., CHEMTRUST INDUSTRIES CORPORATION, A DE CORP.
Assigned to SYSTEMS GENERAL, INC. reassignment SYSTEMS GENERAL, INC. CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). EFFECTIVE JAN. 12, 1987 Assignors: SYSTEMS GENERAL CORPORATION
Assigned to KEM ACQUISITION, INC., 2727 CHEMSEARCH BLVD., IRVING, TEXAS 75062 reassignment KEM ACQUISITION, INC., 2727 CHEMSEARCH BLVD., IRVING, TEXAS 75062 ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: KEM MANUFACTURING CORPORATION, A GA CORP.
Anticipated expiration legal-status Critical
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Classifications

    • 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
    • C11D3/0094High foaming 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
    • C11D3/43Solvents

Definitions

  • This invention relates to stable, clear, nonflammable, water and organic solvent based foamable cleaning compositions.
  • organic solvent based cleaners apart from the flammable nature thereof, manifest very poor, if any, foaming action, a characteristic which detracts from their utility for removing soil and grease from vertical and overhead surfaces where retention of the cleaner is needed to provide adequate cleaning action. It is also known that water based cleaners containing salts which impart foaming properties to the cleaners have a low tolerance for organic solvents. It is further known that organic solvent based cleaners demonstrate a very low capacity for salts of the type usually employed in water based cleaners.
  • compositions have been evolved which incorporate, in a single product, the excellent cleansing action of organic solvent based cleaners, and the cleansing and foaming action of water based cleaners.
  • the compositions furtherrnore, are non-flammable. In addition, they are clear and homogeneous in appearance, and remain stable for prolonged periods of time over a wide temperature range.
  • the water and organic solvent based foamable cleaning compositions of this invention contain, as essential ingredients, (1) water, (2) organic solubilizing agent, most advantageously a mixture of organic solubilizing agents, (3) surfactant preferably in the form of a mixture of a water soluble alkali metal salt or lower alkanolamine salt of a higher alkyl aromatic sulfonic acid and an alkali metal salt of a higher alkyl diphenyl ether sulfonic acid, (4) hydrocarbon solvent, (5) chlorinated solvent, and (6) inorganic builder. Supplemental materials of various types, referred to hereinafter, may be incorporated into the compositions but they are not essential.
  • the organic solubilizing agents utilized in the compositions include lower alkyl ethers of glycols and polyglycols exemplified by monomethyl ether of ethylene glycol, monoethyl ether of ethylene glycol, monobutyl ether of ethylene glycol, monobutyl ether of diethylene glycol, monoisopropyl ether of diethylene glycol, monobutyl ether of butylene glycol, and, as indicated above, most advantageously, mixtures of any of the foregoing ethers with glycols such as ethylene glycol, propylene glycol, hexylene glycol, heptylene glycol, and the like.
  • a mixture comprising monobutyl ether of ethylene glycol and hexylene glycol is preferred.
  • the proportions of solubilizer employed will range from about 3% to about 30%, usually about 10% to about 18%, by weight, of the composition.
  • the solubilizer comprises a mixture of an ether such as monobutyl ether of ethylene glycol and a glycol such as hexylene glycol
  • the proportion of ether desirably will range from about 1% to about and the glycol from about 2% to about 15%, by weight, of the composition.
  • the surfactants used in the compositions include water soluble alkali metal and lower alkanolamine salts of alkyl benzene or toluene sulfonic acids in which the alkyl group contains predominately from eight to 22 carbon atoms, especially desirably predominately 12 to 16 carbon atoms.
  • Particularly preferred are the alkali metal, especially sodium and potassium, and the lower alkanolamine salts of C to C benzene, toluene, ethyl butanolamine, isobutanolarnine, and the like.
  • triethanolamine salts of alkyl benzene sulfonic acids are especially satisfactory.
  • the surfactants having utility for the purposes of this invention also include alkali metal salts of alkyl diphenyl ether sulfonic acids in which the alkyl group has a number of carbon atoms corresponding to the carbon atoms in the alkyl group of the aforementioned alkanolamine salts.
  • alkali metal salts are sodium decyl diphenyl ether disulfonate, sodium dodecyl diphenyl ether disulfonate, sodium tetradecyl diphenyl ether disulfonate, and the like.
  • the surfactant component of the compositions advantageously comprises a mixture which includes at least one alkali metal or alkanolamine salt of an alkyl benzene sulfonic acid and at least one alkali metal, sodium, in particular, salt of an alkyl diphenyl ether disulfonate.
  • the proportions of surfactant utilized in the compositions can range from about 7% to about 30%, usually from about 10% to about 20%, by weight, of the composition.
  • the surfactant employed comprises a mixture of an alkyli metal or alkanolamine salt of an alkyl benzene sulfonic acid such as triethanolarnine dodecyl benzene sulfonate and an alkali metal salt of an alkyl diphenyl ether sulfonic acid such as sodium decyl diphenyl ether disulfonate
  • the proportion of the alkali metal or alkanolamine salt can range from about 7% to 20%, by weight, of the composition
  • the proportion of the alkali metal salt of the diphenyl ether sulfonic acid can range from about 1% to 10%, by weight, of the composition.
  • hydrocarbon solvents useful in the preparation of the compositions comprise petroleum derived paraffinic and cycloparaffinic hydrocarbons exemplary of which are kerosene, Nos. 1 and 2 distillate fuel oils, petroleum aliphatic solvents such as Varsol, mineral spirits, Stoddard solvent, and the like. Also useful are aromatic hydrocarbon solvents such as benzene, toluene, xylenes, and aromatic petroleum solvents examples of which are SC Solvents No. 1, No. l-A, No. 2, and the like.
  • the proportions of hydrocarbon solvent utilized will range from about 1% to about 20%, especially desirably from about 5% to about 15%, by weight, of the composition.
  • the chlorinated solvents employed in the compositions include chlorine substituted aliphatic hydrocarbons having from 1 to 6 carbon atoms which are liquid at room temperature.
  • exemplary of such solvents are methylene chloride, ethylene dichloride, carbon tetrachloride, 1,2-dichloroethane, l,l,l-trichloroethane, 1,3-dichloropropane, chloroform, 1,4-dichlorobutane, perchloroethylene, trichloroethylene, and the like.
  • freon-type halogenated hydrocarbons such as trichloromonofluoromethane (Freon 11) and trichlorotrifluoroethane (freon 113).
  • Other chlorinated solvents which can be used are the proprietary chlorinated solvents sold under the trademarks CLOROETHENE and DOWCLENE (Dow Chemical Company). Of the foregoing, methylene chloride is the preferred chlorinated solvent.
  • the proportions of chlorinated solvent used in the preparation of the compositions will range from about 1% to about 25%, usually from about 5% to about by weight, of the composition. While the proportions of hydrocarbon solvent and chlorinated solvent employed can range, as stated, from about 1% to about and from about 1% to about respectively, by weight, of the compositions, especially satisfactory results are attained with combined proportions of the two solvents ranging fromabout 3% to about 40%, by weight, of the compositions.
  • the inorganic builders used in the compositions of this invention include alkali metal silicates, borates, carbonates, nitrites, sulfates, polyphosphates, metaphosphates, orthophosphates and pyrophosphates such as sodium silicate, sodium metasilicate, sodium orthosilicate, sodium tetraborate, sodium borate, sodium sulfate, sodium carbonate, trisodium phosphate, disodium orthophosphate, sodium metaphosphate, sodium nitrite, sodium pyrophosphate, potassium pyrophosphate, and the like.
  • the proportions of inorganic builders incorporated into the compositions will range from about 0.5% to about 6%, usually from about 2% to about 4%, by weight, of the composition.
  • the inorganic builders among other things, act to enhance the soil removal and suspension properties of the compositions.
  • supplemental ingredients can be added to the foamable compositions of this invention.
  • These comprise, for example, germicides, sequestering agents for greater hard water tolerance, coloring dyes, perfumes, and the like, all of which when utilized, are employed in small amounts, most of them below 1%, by weight, of the composition.
  • a stable, clear, non-flammable, water and organic solvent based foamable cleaning composition consisting essentially of, in approximately the stated percentages by weight:

Abstract

Stable, clear, non-flammable, water and organic solvent based foamable cleaning compositions comprising water, hydrocarbon solvent, chlorinated solvent, surfactant, organic solubilizing agent and builder.

Description

United States Patent [191 Ancel et al.
[451 Oct. 28, 1975 CLEANING COMPOSITIONS [75] Inventors: Selwyn J. Ancel, River Forest;
James O. Gladish, Glenview; Floyd L. Mickelson, Chicago, all of Ill. [73] Assignee: Chemtrust Industries Corporation,
Franklin Park, Ill.
[22] Filed: Aug. 29, 1973 g 21 Appl. No.1 392,647
[52] US. Cl. 252/526; 252/118; 252/139; 252/153; 252/162; 252/166; 252/545; 252/DIG. 8; 252/DIG. 14 [51] Int. Cl. CllD 3/066 [58] Field of Search 252/526, 162, 166, 139, ZSZ/DIG. 8, DIG. 14, 545, 153, 118
[56] References Cited UNITED STATES PATENTS 3,232,880 2/1966 Mausner et a]. 252/DIG. 14
3,634,272 1/1972 Valenta et al. 252/153 3,634,338 l/l972 Laugle et a]. i. 252/539 X 3,835,070 9/1974 Beck 252/526 Primary Examiner-Benjamin R. Padgett Assistant E.\'aminer E. Suzanne Parr Attorney, Agent, or FirmWallenstein, Spangenberg, Hattis & Strampel [57] ABSTRACT Stable, clear, non-flammable, water and organic solvent based foamable cleaning compositions comprising water, hydrocarbon solvent, chlorinated solvent, surfactant, organic solubilizing agent and builder.
1 Claim, No Drawings CLEANING COMPOSITIONS This invention relates to stable, clear, nonflammable, water and organic solvent based foamable cleaning compositions.
It is known that organic solvent based cleaners, apart from the flammable nature thereof, manifest very poor, if any, foaming action, a characteristic which detracts from their utility for removing soil and grease from vertical and overhead surfaces where retention of the cleaner is needed to provide adequate cleaning action. It is also known that water based cleaners containing salts which impart foaming properties to the cleaners have a low tolerance for organic solvents. It is further known that organic solvent based cleaners demonstrate a very low capacity for salts of the type usually employed in water based cleaners.
In accordance with the present invention compositions have been evolved which incorporate, in a single product, the excellent cleansing action of organic solvent based cleaners, and the cleansing and foaming action of water based cleaners. The compositions, furtherrnore, are non-flammable. In addition, they are clear and homogeneous in appearance, and remain stable for prolonged periods of time over a wide temperature range.
The water and organic solvent based foamable cleaning compositions of this invention contain, as essential ingredients, (1) water, (2) organic solubilizing agent, most advantageously a mixture of organic solubilizing agents, (3) surfactant preferably in the form of a mixture of a water soluble alkali metal salt or lower alkanolamine salt of a higher alkyl aromatic sulfonic acid and an alkali metal salt of a higher alkyl diphenyl ether sulfonic acid, (4) hydrocarbon solvent, (5) chlorinated solvent, and (6) inorganic builder. Supplemental materials of various types, referred to hereinafter, may be incorporated into the compositions but they are not essential.
The organic solubilizing agents utilized in the compositions include lower alkyl ethers of glycols and polyglycols exemplified by monomethyl ether of ethylene glycol, monoethyl ether of ethylene glycol, monobutyl ether of ethylene glycol, monobutyl ether of diethylene glycol, monoisopropyl ether of diethylene glycol, monobutyl ether of butylene glycol, and, as indicated above, most advantageously, mixtures of any of the foregoing ethers with glycols such as ethylene glycol, propylene glycol, hexylene glycol, heptylene glycol, and the like. In the latter case, a mixture comprising monobutyl ether of ethylene glycol and hexylene glycol is preferred. The proportions of solubilizer employed will range from about 3% to about 30%, usually about 10% to about 18%, by weight, of the composition. When the solubilizer comprises a mixture of an ether such as monobutyl ether of ethylene glycol and a glycol such as hexylene glycol, the proportion of ether desirably will range from about 1% to about and the glycol from about 2% to about 15%, by weight, of the composition.
The surfactants used in the compositions include water soluble alkali metal and lower alkanolamine salts of alkyl benzene or toluene sulfonic acids in which the alkyl group contains predominately from eight to 22 carbon atoms, especially desirably predominately 12 to 16 carbon atoms. Particularly preferred are the alkali metal, especially sodium and potassium, and the lower alkanolamine salts of C to C benzene, toluene, ethyl butanolamine, isobutanolarnine, and the like. Of the foregoing, triethanolamine salts of alkyl benzene sulfonic acids are especially satisfactory. The surfactants having utility for the purposes of this invention also include alkali metal salts of alkyl diphenyl ether sulfonic acids in which the alkyl group has a number of carbon atoms corresponding to the carbon atoms in the alkyl group of the aforementioned alkanolamine salts. Exemplary of such alkali metal salts are sodium decyl diphenyl ether disulfonate, sodium dodecyl diphenyl ether disulfonate, sodium tetradecyl diphenyl ether disulfonate, and the like. In accordance with the preferred embodiments of the invention, the surfactant component of the compositions advantageously comprises a mixture which includes at least one alkali metal or alkanolamine salt of an alkyl benzene sulfonic acid and at least one alkali metal, sodium, in particular, salt of an alkyl diphenyl ether disulfonate.
The proportions of surfactant utilized in the compositions can range from about 7% to about 30%, usually from about 10% to about 20%, by weight, of the composition. In those instances where, as indicated, the surfactant employed comprises a mixture of an alkyli metal or alkanolamine salt of an alkyl benzene sulfonic acid such as triethanolarnine dodecyl benzene sulfonate and an alkali metal salt of an alkyl diphenyl ether sulfonic acid such as sodium decyl diphenyl ether disulfonate, the proportion of the alkali metal or alkanolamine salt can range from about 7% to 20%, by weight, of the composition, while the proportion of the alkali metal salt of the diphenyl ether sulfonic acid can range from about 1% to 10%, by weight, of the composition.
The hydrocarbon solvents useful in the preparation of the compositions comprise petroleum derived paraffinic and cycloparaffinic hydrocarbons exemplary of which are kerosene, Nos. 1 and 2 distillate fuel oils, petroleum aliphatic solvents such as Varsol, mineral spirits, Stoddard solvent, and the like. Also useful are aromatic hydrocarbon solvents such as benzene, toluene, xylenes, and aromatic petroleum solvents examples of which are SC Solvents No. 1, No. l-A, No. 2, and the like. The proportions of hydrocarbon solvent utilized will range from about 1% to about 20%, especially desirably from about 5% to about 15%, by weight, of the composition.
The chlorinated solvents employed in the compositions include chlorine substituted aliphatic hydrocarbons having from 1 to 6 carbon atoms which are liquid at room temperature. Exemplary of such solvents are methylene chloride, ethylene dichloride, carbon tetrachloride, 1,2-dichloroethane, l,l,l-trichloroethane, 1,3-dichloropropane, chloroform, 1,4-dichlorobutane, perchloroethylene, trichloroethylene, and the like. Also useful are freon-type halogenated hydrocarbons such as trichloromonofluoromethane (Freon 11) and trichlorotrifluoroethane (freon 113). Other chlorinated solvents which can be used are the proprietary chlorinated solvents sold under the trademarks CLOROETHENE and DOWCLENE (Dow Chemical Company). Of the foregoing, methylene chloride is the preferred chlorinated solvent.
The proportions of chlorinated solvent used in the preparation of the compositions will range from about 1% to about 25%, usually from about 5% to about by weight, of the composition. While the proportions of hydrocarbon solvent and chlorinated solvent employed can range, as stated, from about 1% to about and from about 1% to about respectively, by weight, of the compositions, especially satisfactory results are attained with combined proportions of the two solvents ranging fromabout 3% to about 40%, by weight, of the compositions.
The inorganic builders used in the compositions of this invention include alkali metal silicates, borates, carbonates, nitrites, sulfates, polyphosphates, metaphosphates, orthophosphates and pyrophosphates such as sodium silicate, sodium metasilicate, sodium orthosilicate, sodium tetraborate, sodium borate, sodium sulfate, sodium carbonate, trisodium phosphate, disodium orthophosphate, sodium metaphosphate, sodium nitrite, sodium pyrophosphate, potassium pyrophosphate, and the like. The proportions of inorganic builders incorporated into the compositions will range from about 0.5% to about 6%, usually from about 2% to about 4%, by weight, of the composition. The inorganic builders among other things, act to enhance the soil removal and suspension properties of the compositions.
As stated above, various supplemental ingredients, optional but desirable, can be added to the foamable compositions of this invention. These comprise, for example, germicides, sequestering agents for greater hard water tolerance, coloring dyes, perfumes, and the like, all of which when utilized, are employed in small amounts, most of them below 1%, by weight, of the composition.
The following examples are illustrative of particularly preferred embodiments of the invention. It should be understood that variations may be made therein in a number of particulars without in any way departing from the fundamental principles and teachings provided herein. The examples, therefore, are not to be construed in any way as limitative of the scope of the invention.
EXAMPLE I Ingredient Weight Percent Water 54 Hexylene glycol 2 Monobutyl ether of ethylene glycol 8 Sodium decyl diphenyl ether disulfonate 3 Triethanolamine dodecyl benzene sulfonate 13 Sodium silicate 4 Kerosene (deodorized) l2 Methylene chloride 4 EXAMPLE II Water 55 Hexylene glycol 5 Monoethyl ether of ethylene glycol 5 Sodium dodecyl diphenyl ether disulfonate 4 Sodium dodecyl benzene sulfonate 16 Sodium sulfate 3 SC solvent No. l 7 l ,2-dichloroethane 5 EXAMPLE III Water Heptylene glycol 3 Monobutyl ether of ethylene glycol EXAMPLE III-Continued Sodium dodecyl diphenyl ether disulfonate Triethanolamine dodecyl benzene sulfonate Sodium pyrophosphate Benzene Perchloroethylene I-l (nu-INCA What is claimed is:
1. A stable, clear, non-flammable, water and organic solvent based foamable cleaning composition, consisting essentially of, in approximately the stated percentages by weight:

Claims (1)

1. A STABLE, CLEAR, NON-FLAMMABLE, WATER AND ORGANIC SOLVENT BASED FORMABLE CLEANING COMPOSITION, CONSISTING ESSENTIALLY OF, IN APPROXIMATELY THE STATED PERCENTAGES BY WEIGHT:
US392647A 1973-08-29 1973-08-29 Cleaning compositions Expired - Lifetime US3915902A (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
US392647A US3915902A (en) 1973-08-29 1973-08-29 Cleaning compositions
GB3661774A GB1438447A (en) 1973-08-29 1974-08-20 Cleansing method and composition therefor
DE2440608A DE2440608A1 (en) 1973-08-29 1974-08-23 CLEANING PREPARATION
FR7429091A FR2242461B3 (en) 1973-08-29 1974-08-26
IT26650/74A IT1020225B (en) 1973-08-29 1974-08-27 CLEANING COMPOSITIONS
JP49098808A JPS5072905A (en) 1973-08-29 1974-08-28

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US3915902A true US3915902A (en) 1975-10-28

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JP (1) JPS5072905A (en)
DE (1) DE2440608A1 (en)
FR (1) FR2242461B3 (en)
GB (1) GB1438447A (en)
IT (1) IT1020225B (en)

Cited By (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4097397A (en) * 1976-10-27 1978-06-27 Kao Soap Co., Ltd. Dry cleaning detergent composition
US4219333A (en) * 1978-07-03 1980-08-26 Harris Robert D Carbonated cleaning solution
US4302365A (en) * 1980-02-11 1981-11-24 American Grease Stick Company Engine degreaser composition
US4306989A (en) * 1979-10-09 1981-12-22 Lift-Off, Inc. Composition for releasing adhesives from a surface
US4501682A (en) * 1982-12-17 1985-02-26 Edward Goodman Cleaning and protective composition and method
US4543206A (en) * 1984-05-03 1985-09-24 Adams Cornell L Nail lacquer and enamel remover
US4592856A (en) * 1983-11-14 1986-06-03 Shin-Etsu Chemical Co., Ltd. Liquid detergent composition
US4652389A (en) * 1984-12-14 1987-03-24 The Clorox Company Carpet cleaner
US4676920A (en) * 1985-08-06 1987-06-30 Stephen Culshaw Creamy scouring compositions
US4780100A (en) * 1984-12-14 1988-10-25 The Clorox Company Fabric cleaner
US4810411A (en) * 1986-04-16 1989-03-07 E. I. Du Pont De Nemours And Company Solvent-based fabric protector
WO1994003571A1 (en) * 1992-07-31 1994-02-17 Henkel Corporation Process and aqueous composition for degreasing metal surface
US5454969A (en) * 1993-06-18 1995-10-03 Fields; Paul B. Cleaning fluids
US5651830A (en) * 1993-02-01 1997-07-29 Total Service Co., Inc. Method for cleaning surface of external wall of building
US5674827A (en) * 1994-01-11 1997-10-07 Mitsubishi Chemical Corporation Degreasing cleaner and method for cleaning oil-deposited material
US5741997A (en) * 1985-07-01 1998-04-21 Minnesota Mining And Manufacturing Company Low polydispersity glycidyl azide polymer
US6315949B1 (en) 1999-12-30 2001-11-13 Robert Carmello Composition for carpet and room deodorizer and method of delivering the composition
US20030130146A1 (en) * 2002-01-09 2003-07-10 Egbe Matthew I. Aqueous stripping and cleaning composition
US20130338420A1 (en) * 2012-06-19 2013-12-19 The Procter & Gamble Company Surfactant Composition and Method for Decontamination

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0330379A3 (en) * 1988-02-26 1990-04-18 The British Petroleum Company p.l.c. Cleansing compositions

Citations (4)

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Publication number Priority date Publication date Assignee Title
US3232880A (en) * 1961-04-10 1966-02-01 Ultra Chemical Works Inc Liquid detergent composition
US3634272A (en) * 1968-10-25 1972-01-11 Dow Chemical Co Systems for solubilizing water and halogenated aliphatic hydrocarbons
US3634338A (en) * 1970-07-10 1972-01-11 Grace W R & Co Method and composition for cleaning aluminum magnesiumand alloys thereof
US3835070A (en) * 1972-04-17 1974-09-10 Diamond Shamrock Corp Hard surface cleaners

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3232880A (en) * 1961-04-10 1966-02-01 Ultra Chemical Works Inc Liquid detergent composition
US3634272A (en) * 1968-10-25 1972-01-11 Dow Chemical Co Systems for solubilizing water and halogenated aliphatic hydrocarbons
US3634338A (en) * 1970-07-10 1972-01-11 Grace W R & Co Method and composition for cleaning aluminum magnesiumand alloys thereof
US3835070A (en) * 1972-04-17 1974-09-10 Diamond Shamrock Corp Hard surface cleaners

Cited By (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4097397A (en) * 1976-10-27 1978-06-27 Kao Soap Co., Ltd. Dry cleaning detergent composition
US4219333A (en) * 1978-07-03 1980-08-26 Harris Robert D Carbonated cleaning solution
US4306989A (en) * 1979-10-09 1981-12-22 Lift-Off, Inc. Composition for releasing adhesives from a surface
US4302365A (en) * 1980-02-11 1981-11-24 American Grease Stick Company Engine degreaser composition
US4501682A (en) * 1982-12-17 1985-02-26 Edward Goodman Cleaning and protective composition and method
US4592856A (en) * 1983-11-14 1986-06-03 Shin-Etsu Chemical Co., Ltd. Liquid detergent composition
US4543206A (en) * 1984-05-03 1985-09-24 Adams Cornell L Nail lacquer and enamel remover
US4780100A (en) * 1984-12-14 1988-10-25 The Clorox Company Fabric cleaner
US4652389A (en) * 1984-12-14 1987-03-24 The Clorox Company Carpet cleaner
US5741997A (en) * 1985-07-01 1998-04-21 Minnesota Mining And Manufacturing Company Low polydispersity glycidyl azide polymer
US4676920A (en) * 1985-08-06 1987-06-30 Stephen Culshaw Creamy scouring compositions
US4810411A (en) * 1986-04-16 1989-03-07 E. I. Du Pont De Nemours And Company Solvent-based fabric protector
WO1994003571A1 (en) * 1992-07-31 1994-02-17 Henkel Corporation Process and aqueous composition for degreasing metal surface
US5651830A (en) * 1993-02-01 1997-07-29 Total Service Co., Inc. Method for cleaning surface of external wall of building
US5454969A (en) * 1993-06-18 1995-10-03 Fields; Paul B. Cleaning fluids
US5674827A (en) * 1994-01-11 1997-10-07 Mitsubishi Chemical Corporation Degreasing cleaner and method for cleaning oil-deposited material
US6315949B1 (en) 1999-12-30 2001-11-13 Robert Carmello Composition for carpet and room deodorizer and method of delivering the composition
US20030130146A1 (en) * 2002-01-09 2003-07-10 Egbe Matthew I. Aqueous stripping and cleaning composition
US6943142B2 (en) * 2002-01-09 2005-09-13 Air Products And Chemicals, Inc. Aqueous stripping and cleaning composition
US20050217697A1 (en) * 2002-01-09 2005-10-06 Egbe Matthew I Aqueous stripping and cleaning composition
US8231733B2 (en) 2002-01-09 2012-07-31 Air Products And Chemicals, Inc. Aqueous stripping and cleaning composition
US20130338420A1 (en) * 2012-06-19 2013-12-19 The Procter & Gamble Company Surfactant Composition and Method for Decontamination
US9295865B2 (en) * 2012-06-19 2016-03-29 TOA Research, Inc. Surfactant composition and method for decontamination

Also Published As

Publication number Publication date
FR2242461A1 (en) 1975-03-28
FR2242461B3 (en) 1977-06-17
IT1020225B (en) 1977-12-20
GB1438447A (en) 1976-06-09
DE2440608A1 (en) 1975-03-13
JPS5072905A (en) 1975-06-16

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