US3265625A - Liquid detergent - Google Patents

Liquid detergent Download PDF

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US3265625A
US3265625A US234240A US23424062A US3265625A US 3265625 A US3265625 A US 3265625A US 234240 A US234240 A US 234240A US 23424062 A US23424062 A US 23424062A US 3265625 A US3265625 A US 3265625A
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weight
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alcohol
condensate
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US234240A
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Grob Erwin
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C P Baker & Co
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C P Baker & Co
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    • 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
    • C11D3/16Organic compounds
    • C11D3/26Organic compounds containing nitrogen
    • C11D3/33Amino carboxylic acids
    • 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
    • C11D1/34Derivatives of acids of phosphorus
    • C11D1/345Phosphates or phosphites
    • 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
    • C11D1/52Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
    • C11D1/523Carboxylic alkylolamides, or dialkylolamides, or hydroxycarboxylic amides (R1-CO-NR2R3), where R1, R2 or R3 contain one hydroxy group per alkyl group
    • 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
    • C11D1/66Non-ionic compounds
    • C11D1/72Ethers of polyoxyalkylene glycols
    • 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
    • C11D3/16Organic compounds
    • C11D3/34Organic compounds containing sulfur
    • C11D3/3418Toluene -, xylene -, cumene -, benzene - or naphthalene sulfonates or sulfates

Description

United States Patent 3,265,625 LIQUID DETERGENT Erwin Grob, Philadelphia, Pa., assignor to C. P. Baker & Company, Philadelphia, Pa., a corporation of Pennsylvania No Drawing. Filed Oct. 30, 1962, Ser. No. 234,240 9 Claims. (Cl. 252-152) This invention relates to liquid detergents and more particularly to substantially clear, homogeneous aqueous compositions of high concentration for home laundering and general cleaning use.
The essential active ingredients in these aqueous detergents are surfactants and salts of aminocar-boxylic acids.
The liquid detergent composition of this invention otters several advantages over the granular detergent compositions, such as, to name a \few, freedom from dust, ease of measuring the proper amount for optimum performance, pre-trea-ting of heavily soiled items by spotting them with the undiluted product before placing these items in the washing machine and a soft feel imparted to laundered cotton goods.
Prior art liquid detergents utilized large quantities of inorganic phosphate builders. The preparation of such products Was relatively diificult; sometimes large quantities of hydrotropes were required to produce stable compositions and the amount and type of surfactant was often dictated by limited compatibility of surfactant and phosphate builder.
it is an object of this invention to provide an effective liquid detergent utilizing organic builders or sequestrants in relatively smaller amounts. The detergent compositions of this invention are stable products at room temperature, exhibiting high 'detergency with moderate to little sudsing in automatic Washing machines. Most of the components making up this invention are supplied in liquid tform facilitating the manufiacture of the end product by requiring only conventional equipment.
The detergents of this invention generally comprise aqueous compositions containing by weight:
A. 4-15 of an alkali metal salt of an aminocarboxylic acid or a mixture of two salts of such acids.
B. 5-15 of a nonionic surfactant of the type of an al-kyl aryl polyether alcohol.
C. 1-1-0% of a phosphate ester modified by the addition of alkylene oxides.
:D. 2-8% of a fatty acid alkanolamine condensate.
The remainder of the composition is Water which may include such optional constituents as optical brighteners, dyes, and perfumes and the like as is known in the art.
(In compositions wherein the concentration of active ingredients exceeds about 20% by weight, it is necessary to include as a solubilizing agent trom 1 to by weight of an alkali metal salt of a short chain alkyl aryl sulfonic acid to yield homogeneous, stable compositions.
The compositions as prepared have a pH of about 8 and it is desirable to add alkali to adjust the pH in range of 10 to 11.
Suitable materials utilizable as component A include the alkali metal salts of ethylenediamine tetra acetic acid such as trisodium ethylenediamine tetraacetate, trisodium hydroxyethyl ethylene-diamine triacetate, penta sodium diethylenetriamine pentaacetate and the like. Suitable materials also are the alkali metal salts of nitrilotriacetic acid such as the mono, 'di or trisodium or potassium salts. Mixtures of two or more aminocarboxylates may be used. The materials may be utilized in the torm of powders or, more conveniently, as aqueous solutions.
As component B one may use the nonionic alkyl aryl polyether alcohols such as tertiary octyl phenoxy polyethoxy ethanol containing 6-20 ethylene oxide units per mole, or nonylphenoxy polyethoxy ethanol containing iirom 6-20 ethylene oxide units per molecule. These materials are supplied as essentially active liquids.
Suitable materials useable as component C include pnonylphenol condensed with 5-20 moles ethylene oxide which is then esterified with orthophosphoric acid. Additional phosphate esters include those based on tridecyl alcohol condensed with 5-20 moles of ethylene'oiiide, as
well as those based on C to C al-kylphenols condensed with ethylene oxide. They may be used in the iorm of the free acid or as the alkali metal salt. These materials are supplied as essentially 100% active liquids.
Component D is a so called Krit-chevs-ky condensate of a C to C fatty acid with ethanolamine, propanolamine, diethanolamine and the like. They are mixtures of alkanolamides with alkanolamine soaps of tatty acids and are substantially :100% active liquids.
For more concentrated compositions requiring the use of a solubilizing agent or hydrotrope, the sodium or potassium salts of xylene sulfonic acid, toluene sulfonic acid or benzene sulfonic acid may be used.
The alkali [for adjusting the pH may be potassium hydroxide, sodium hydroxide, ammonia or amines. 'Usually about 0.5% by weight is required.
Suitable optical brighteners which may be optionally included are the well known stilbene derivatives, such as 4,4'-di'benzoyl \diamino stilbene 2,2 disul fonic acid. They are usually employed in the range of 0.1 to 0.5 by weight.
A preferred procedure for mixing the ingredients is as follows:
To the required amount of water is added the optical brightener, if any, and dispersed with agitation. Then about one-fourth of component A is added with agitation following in succession by the solubilizing agent, if any, and components B, C, and D. Then the remaining threetourths of component A are added and the composition neutralized and the pH adjusted to pH 10-11 by the addition of alkali. The end product may be dyed and perfumed as desired. The resulting product is a clear liquid, stable at room temperature, only moderately viscous and highly concentrated. The product is economical to use; two to three liquid ounces are a sufiicient amount for a top loading automatic washing machine of 12-14 gallons water capacity.
The iollowing examples illustrate the practice of the invention, in which all parts are by weight. Compositions were prepared consisting of the following:
Components on percent active basis by weight Examples I II III IV V VI VII VIII In the above examples, the pH was adjusted to about pH 10.5 with potassium hydroxide. The optical brightener in the examples was 4,4'-dibenzoyl diamino stilbene- 2,2'-disul-fonic acid.
Compositions I, II, and III are highly concentrated formulations with moderate sudsing. Compositions IV and V are highly concentrated, but little sudsing. Compositions VI, VII, and VIII are more diluted compositions, but excellent detergents.
Example IX The following composition was prepared:
Parts p-Nonyl phenoxy polyethoxy ethanol (14 ethoxy units) 12 Laurie acid-diethanolamine condensate p-Nonyl phenol phosphate-ethylene oxide condensate mols ethylene oxide) 5 Sodium toluene sulfonate 5 Tetrasodium ethylenediamine tetraacetate 2 Trisodium nitrilotriacetate 8 Water to 100.
The above was a clear, heavy duty, moderately sudsing laundry detergent.
While the invention has been described in terms of certain examples, they are to be considered illustrative rather than limiting, and it is intended to cover all further embodiments and modifications apparent to those skilled in the art that fall within the spirit of the claims.
I claim:
1. A substantially clear, homogeneous liquid detergent consisting of about 1 to 5% by weight of trisodium hydroxyethyl ethylenediamine triacetate, about 1 to 10% by weight of sodium xylene sulfonate, about 5 to by Weight of oetyl phenol condensed with 12 to 13 moles of ethylene oxide, per mole of phenol about 1 to 10% by weight of the phosphate ester of tridecyl alcoholethylene oxide condensate, having 5 to ethoxy groups per mole of alcohol about 2 to 8% by weight of coconut fatty acid-diethanolamine condensate, about 4 to 10% by weight of trisodium nitrilotriacetate and the remainder water.
2. A substantially clear, homogeneous liquid detergent consisting of about 2.05% by weight of trisodium hydroxyethyl ethylenediamine triacetate, about 5% by weight of sodium xylene sulfonate, about 12% by weight of oetyl phenol condensed with 12 to 13 moles of ethylene oxide, per mole of phenol about 5% by weight of the phosphate ester of tridecyl alcohol-ethylene oxide condensate, having 5 to 20 ethoxy groups per mole of alcohol about 7% by weight of coconut fatty acid-diethanolamine condensate, about 7.5% by weight of trisodium nitrilotriacetate, and the remainder water.
3. A substantially clear, homogeneous liquid detergent consisting of about 5 to 15% by weight of an alkylphenolethylene oxide condensate having 6 to 20 ethoxy groups per mole of phenol and the alkyl group having 8 to 9 carbon atoms nonionic detergent, about 1 to 10% by weight of a long chain alcohol-ethylene oxide condensate having 5 to 20 ethoxy groups per mole of alcohol esterified with phosphoric acid, said long chain alcohol being selected from the group consisting of tridecyl alcohol and alkyl phenols having 8 to 20 carbon atoms in' the alkyl group, about 2 to 8% by weight of a fatty acid-alkanolamine condensate, the fatty acid having 12 to 16 carbon atoms and the alkanolamine being selected from the group consisting of ethanolamine, diethanolamine and propanolamine, about 4 to 15% of an alkali metal salt of an aminopolyacetic acid selected from the group consisting of nitrilotriacetic acid, ethylenediamine tetraaeetic acid, hydroxyethyl ethyl-diamine triacetic acid, and diethy-lenetriamine pentaacetic acid and the remainder Water.
4. A detergent composition set forth in claim 3 including about 1 to 10% by weight of a solubilizing agent selected from the group consisting alkali metal salts of toluene sulfonic acid and alkali metal salts of xylene sulfonic acid.
5. A deter-gent composition set forth in claim 3 where the nonionie detergent is tert.-octylphenoxy polyethoxy ethanol with from 6 to 20 moles of ethylene oxide per mole of phenol.
6. A detergent composition set forth in claim 3 where the nonionic detergent is nonylphenoxy polyethoxy ethanol with from 6 to 20 moles of ethylene oxide per mole of phenol.
'7. A detergent composition set forth in claim 3 where the salt of the aminocarboxylic acid is sodium ethylenediamine tetraacetate.
8. A detergent composition set forth in claim 3 where the salt of the aminocarboxylic acid is sodium nitrilotriacetate.
9. A substantially clear, homogeneous liquid detergent consisting essentially of about 12% by weight p-nonyl phenoxy polyethoxy ethanol having 14 ethoxy units per mole of phenol, about 5% by weight of lauric aciddiethanolamine condensate, about 5% by weight of the phosphate ester of p-nonyl phenol condensed with 10 moles of ethylene oxide per mole of phenol, about 5 by Weight of sodium toluene sulfonate, about 2% by weight of tetrasodium ethylene diamine tetraacetate, about 8% by weight of trisodium nitrilotriacetate, and remainder water.
References Cited by the Examiner UNITED STATES PATENTS 2,089,212 8/ 1937 Kritchevsky. 2,859,182 11/1958 Carroll. 2,877,178 3/1959 Bergman et al. 252152 XR 2,943,058 6/1960 Cook 252152 XR 3,001,945 9/1961 Drew et al. 252152 3,033,889 5/1962 Chiddix et al 252-89 XR LEON D. ROSDOL, Primary Examiner.
JULIUS GREENWALD, Examiner.
w. E. SCHULZ, J. GREENWALD, Assistant Examiners.

Claims (1)

  1. 3. A SUBSTANTIALLY CLEAR, HOMOGENOUS LIQUID DETERGENT CONSISTING OF ABOUT 5 TO 15% BY WEIGHT OF AN ALKYLPHENOLETHYLENE OXIDE CONDENSATE HAVING 6 TO 20 ETHOXY GROUPS PER MOLE OF PHENOL AND THE ALKYL GROUP HAVING 8 TO 9 CARBON ATOMS NONIONIC DETERGENT, ABOUT 1 TO 10% BY WEIGHT OF A LONG CHAIN ALCOHOL-ETHYLENE OXIDE CONDENSATE HAVING 5 TO 20 ETHOXY GROUPS PER MOLE OF ALCOHOL ESTERIFIED WITH PHOSPHORIC ACID, SAID LONG CHAIN ALCOHOL BEING SELECTED FROM THE GROUP CONSISTING OF TRIDECYL ALCOHOL AND ALKYL PHENOLS HAVING 8 TO 20 CARBON ATOMS IN THE ALKYL GROUPS, ABOUT 2 TO 8% BY WEIGHT OF A FATTY ACID-ALKANNOLAMINE CONDENSATE, THE FATTY ACID HAVING 12 TO 16 CARBON ATOMS AND THE ALKANOLAMINE BEING SELECTED FROM THE GROUP CONSISTING OF ETHANOLAMINE, DIETHANOLAMINE AND PROPANOLAMINE, ABOUT 4 TO 15% OF AN ALKALI METAL SALT OF AN AMINOPOLYACETIC ACID SELECTED FROM THE GROUP CONSISTING OF NITRILOTRIACETIC ACID, ETHYLENEDIAMINE TETRAACETIC ACID, HYDROXYETHYL ETHLDIAMINE TRIACETIC ACID, AND DIETHYLENETRIAMINE PENTAACETIC ACID AND THE REMAINDER WATER.
US234240A 1962-10-30 1962-10-30 Liquid detergent Expired - Lifetime US3265625A (en)

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Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3763631A (en) * 1971-06-01 1973-10-09 Chemical Detergents Coinc Method and apparatus for removing entrained matter from centrifugal filter media
US3953380A (en) * 1970-10-28 1976-04-27 Colgate-Palmolive Company Liquid detergent
US3956198A (en) * 1972-12-15 1976-05-11 Days-Ease Home Products Corporation Liquid laundry washing-aid
US3966649A (en) * 1972-09-28 1976-06-29 Colgate-Palmolive Company Liquid detergents containing chelidamic acids and salts thereof
DE2715351A1 (en) * 1976-08-23 1978-03-02 Henkel Kgaa Stable liq. low foaming dishwashing concentrates - contg. phosphorus free complexing agent, low foam nonionic surfactant, a hydrotrope and an alkanolamine
US4097305A (en) * 1975-03-14 1978-06-27 Bickmore, Inc. Method for removing bot eggs from animal hair
US4560492A (en) * 1984-11-02 1985-12-24 The Procter & Gamble Company Laundry detergent composition with enhanced stain removal
US4692276A (en) * 1984-06-22 1987-09-08 Schramm Charles H Non-alkaline, foamable bathroom cleaner
WO2004104147A1 (en) * 2003-05-22 2004-12-02 Reckitt Benckiser N.V. Aqueous cleaning compositions
EP2134734A1 (en) * 2007-03-08 2009-12-23 American Sterilizer Company Biodegradable alkaline disinfectant cleaner with analyzable surfactant

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2089212A (en) * 1936-06-08 1937-08-10 Kritchevsky Wolf Hydrotropic fatty material and method of making same
US2859182A (en) * 1956-11-02 1958-11-04 Lever Brothers Ltd Heavy duty liquid detergent composition
US2877178A (en) * 1955-12-20 1959-03-10 Gen Aniline & Film Corp Ampholytic compositions in wet treatments
US2943058A (en) * 1956-10-15 1960-06-28 Diamond Alkali Co Liquid detergent compositions
US3001945A (en) * 1959-04-29 1961-09-26 Procter & Gamble Liquid detergent composition
US3033889A (en) * 1958-10-21 1962-05-08 Gen Aniline & Film Corp Phosphate esters of branched chain alcohols

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2089212A (en) * 1936-06-08 1937-08-10 Kritchevsky Wolf Hydrotropic fatty material and method of making same
US2877178A (en) * 1955-12-20 1959-03-10 Gen Aniline & Film Corp Ampholytic compositions in wet treatments
US2943058A (en) * 1956-10-15 1960-06-28 Diamond Alkali Co Liquid detergent compositions
US2859182A (en) * 1956-11-02 1958-11-04 Lever Brothers Ltd Heavy duty liquid detergent composition
US3033889A (en) * 1958-10-21 1962-05-08 Gen Aniline & Film Corp Phosphate esters of branched chain alcohols
US3001945A (en) * 1959-04-29 1961-09-26 Procter & Gamble Liquid detergent composition

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3953380A (en) * 1970-10-28 1976-04-27 Colgate-Palmolive Company Liquid detergent
US3763631A (en) * 1971-06-01 1973-10-09 Chemical Detergents Coinc Method and apparatus for removing entrained matter from centrifugal filter media
US3966649A (en) * 1972-09-28 1976-06-29 Colgate-Palmolive Company Liquid detergents containing chelidamic acids and salts thereof
US3956198A (en) * 1972-12-15 1976-05-11 Days-Ease Home Products Corporation Liquid laundry washing-aid
US4097305A (en) * 1975-03-14 1978-06-27 Bickmore, Inc. Method for removing bot eggs from animal hair
DE2715351A1 (en) * 1976-08-23 1978-03-02 Henkel Kgaa Stable liq. low foaming dishwashing concentrates - contg. phosphorus free complexing agent, low foam nonionic surfactant, a hydrotrope and an alkanolamine
US4692276A (en) * 1984-06-22 1987-09-08 Schramm Charles H Non-alkaline, foamable bathroom cleaner
EP0181025A2 (en) * 1984-11-02 1986-05-14 The Procter & Gamble Company Laundry detergent composition with enhanced stain removal
JPS61166896A (en) * 1984-11-02 1986-07-28 ザ、プロクタ−、エンド、ギヤンブル、カンパニ− Washing detergent composition having enhanced stain removal property
US4560492A (en) * 1984-11-02 1985-12-24 The Procter & Gamble Company Laundry detergent composition with enhanced stain removal
EP0181025A3 (en) * 1984-11-02 1989-12-13 The Procter & Gamble Company Laundry detergent composition with enhanced stain removal
JPH08918B2 (en) 1984-11-02 1996-01-10 ザ、プロクター、エンド、ギャンブル、カンパニー Laundry detergent composition having enhanced stain removal
WO2004104147A1 (en) * 2003-05-22 2004-12-02 Reckitt Benckiser N.V. Aqueous cleaning compositions
EP2134734A1 (en) * 2007-03-08 2009-12-23 American Sterilizer Company Biodegradable alkaline disinfectant cleaner with analyzable surfactant
EP2134734A4 (en) * 2007-03-08 2012-07-11 American Sterilizer Co Biodegradable alkaline disinfectant cleaner with analyzable surfactant

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