|Número de publicación||US3915902 A|
|Tipo de publicación||Concesión|
|Fecha de publicación||28 Oct 1975|
|Fecha de presentación||29 Ago 1973|
|Fecha de prioridad||29 Ago 1973|
|También publicado como||DE2440608A1|
|Número de publicación||US 3915902 A, US 3915902A, US-A-3915902, US3915902 A, US3915902A|
|Inventores||Ancel Selwyn J, Gladish James O, Mickelson Floyd L|
|Cesionario original||Chemtrust Ind Corp|
|Exportar cita||BiBTeX, EndNote, RefMan|
|Citas de patentes (4), Citada por (23), Clasificaciones (8), Eventos legales (3)|
|Enlaces externos: USPTO, Cesión de USPTO, Espacenet|
United States Patent [191 Ancel et al.
[451 Oct. 28, 1975 CLEANING COMPOSITIONS  Inventors: Selwyn J. Ancel, River Forest;
James O. Gladish, Glenview; Floyd L. Mickelson, Chicago, all of Ill.  Assignee: Chemtrust Industries Corporation,
Franklin Park, Ill.
 Filed: Aug. 29, 1973 g 21 Appl. No.1 392,647
 US. Cl. 252/526; 252/118; 252/139; 252/153; 252/162; 252/166; 252/545; 252/DIG. 8; 252/DIG. 14  Int. Cl. CllD 3/066  Field of Search 252/526, 162, 166, 139, ZSZ/DIG. 8, DIG. 14, 545, 153, 118
 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  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:
|Patente citada||Fecha de presentación||Fecha de publicación||Solicitante||Título|
|US3232880 *||10 Abr 1961||1 Feb 1966||Ultra Chemical Works Inc||Liquid detergent composition|
|US3634272 *||25 Oct 1968||11 Ene 1972||Dow Chemical Co||Systems for solubilizing water and halogenated aliphatic hydrocarbons|
|US3634338 *||10 Jul 1970||11 Ene 1972||Grace W R & Co||Method and composition for cleaning aluminum magnesiumand alloys thereof|
|US3835070 *||17 Abr 1972||10 Sep 1974||Diamond Shamrock Corp||Hard surface cleaners|
|Patente citante||Fecha de presentación||Fecha de publicación||Solicitante||Título|
|US4097397 *||24 Jun 1977||27 Jun 1978||Kao Soap Co., Ltd.||Dry cleaning detergent composition|
|US4219333 *||3 Jul 1978||26 Ago 1980||Harris Robert D||Carbonated cleaning solution|
|US4302365 *||11 Feb 1980||24 Nov 1981||American Grease Stick Company||Engine degreaser composition|
|US4306989 *||9 Oct 1979||22 Dic 1981||Lift-Off, Inc.||Composition for releasing adhesives from a surface|
|US4501682 *||17 Dic 1982||26 Feb 1985||Edward Goodman||Cleaning and protective composition and method|
|US4543206 *||3 May 1984||24 Sep 1985||Adams Cornell L||Nail lacquer and enamel remover|
|US4592856 *||2 Nov 1984||3 Jun 1986||Shin-Etsu Chemical Co., Ltd.||Liquid detergent composition|
|US4652389 *||14 Dic 1984||24 Mar 1987||The Clorox Company||Carpet cleaner|
|US4676920 *||30 Jul 1986||30 Jun 1987||Stephen Culshaw||Creamy scouring compositions|
|US4780100 *||26 Nov 1986||25 Oct 1988||The Clorox Company||Fabric cleaner|
|US4810411 *||23 Jul 1987||7 Mar 1989||E. I. Du Pont De Nemours And Company||Solvent-based fabric protector|
|US5454969 *||4 Nov 1993||3 Oct 1995||Fields; Paul B.||Cleaning fluids|
|US5651830 *||16 Abr 1996||29 Jul 1997||Total Service Co., Inc.||Method for cleaning surface of external wall of building|
|US5674827 *||6 Ene 1995||7 Oct 1997||Mitsubishi Chemical Corporation||Degreasing cleaner and method for cleaning oil-deposited material|
|US5741997 *||30 Dic 1988||21 Abr 1998||Minnesota Mining And Manufacturing Company||Low polydispersity glycidyl azide polymer|
|US6315949||30 Dic 1999||13 Nov 2001||Robert Carmello||Composition for carpet and room deodorizer and method of delivering the composition|
|US6943142 *||9 Ene 2002||13 Sep 2005||Air Products And Chemicals, Inc.||Aqueous stripping and cleaning composition|
|US8231733||27 May 2005||31 Jul 2012||Air Products And Chemicals, Inc.||Aqueous stripping and cleaning composition|
|US9295865 *||6 Jun 2013||29 Mar 2016||TOA Research, Inc.||Surfactant composition and method for decontamination|
|US20030130146 *||9 Ene 2002||10 Jul 2003||Egbe Matthew I.||Aqueous stripping and cleaning composition|
|US20050217697 *||27 May 2005||6 Oct 2005||Egbe Matthew I||Aqueous stripping and cleaning composition|
|US20130338420 *||6 Jun 2013||19 Dic 2013||The Procter & Gamble Company||Surfactant Composition and Method for Decontamination|
|WO1994003571A1 *||16 Jul 1993||17 Feb 1994||Henkel Corporation||Process and aqueous composition for degreasing metal surface|
|Clasificación de EE.UU.||510/428, 510/497|
|Clasificación internacional||C11D3/44, C11D3/43|
|Clasificación cooperativa||C11D3/43, C11D3/0094|
|Clasificación europea||C11D3/43, C11D3/00B19|
|1 Jul 1988||AS02||Assignment of assignor's interest|
Owner name: KEM ACQUISITION, INC., 2727 CHEMSEARCH BLVD., IRVI
Owner name: KEM MANUFACTURING CORPORATION, A GA CORP.
Effective date: 19861219
|1 Jul 1988||AS01||Change of name|
Owner name: KEM ACQUISITION, INC.
Effective date: 19870618
Owner name: SYSTEMS GENERAL CORPORATION
|1 Jul 1988||AS||Assignment|
Owner name: FIRST NATIONAL BANK OF CHICAGO
Free format text: ;ASSIGNORS:CHEMTRUST INDUSTRIES CORPORATION, A DE CORP.;CHEMTRUST INDUSTRIES CORPORATION OF CALIFORNIA, A CA CORP.;REEL/FRAME:004914/0013
Effective date: 19810807
Owner name: KEM ACQUISITION, INC., 2727 CHEMSEARCH BLVD., IRVI
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:KEM MANUFACTURING CORPORATION, A GA CORP.;REEL/FRAME:004914/0021
Effective date: 19861219
Owner name: KEM MANUFACTURING CORPORATION, A GEORGIA CORPORATI
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:FIRST NATIONAL BANK OF CHICAGO, THE, A NATIONAL BANKING ASSOCIATION;REEL/FRAME:004914/0018
Effective date: 19810814
Owner name: SYSTEMS GENERAL CORPORATION
Free format text: CHANGE OF NAME;ASSIGNOR:KEM ACQUISITION, INC.;REEL/FRAME:004914/0023
Owner name: SYSTEMS GENERAL, INC.
Free format text: CHANGE OF NAME;ASSIGNOR:SYSTEMS GENERAL CORPORATION;REEL/FRAME:004914/0025
Effective date: 19870618