US3085982A - Liquid detergent composition - Google Patents

Liquid detergent composition Download PDF

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Publication number
US3085982A
US3085982A US808022A US80802259A US3085982A US 3085982 A US3085982 A US 3085982A US 808022 A US808022 A US 808022A US 80802259 A US80802259 A US 80802259A US 3085982 A US3085982 A US 3085982A
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United States
Prior art keywords
detergent
potassium
sodium
carbon atoms
amine oxide
Prior art date
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Expired - Lifetime
Application number
US808022A
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English (en)
Inventor
David C Steer
Norman R Smith
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Procter and Gamble Co
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Procter and Gamble Co
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Filing date
Publication date
Priority to NL250715D priority Critical patent/NL250715A/xx
Priority to BE622462D priority patent/BE622462A/xx
Priority to DENDAT1185756D priority patent/DE1185756B/de
Application filed by Procter and Gamble Co filed Critical Procter and Gamble Co
Priority to US808022A priority patent/US3085982A/en
Priority to FR824805A priority patent/FR1295354A/fr
Priority to GB14304/60A priority patent/GB951930A/en
Application granted granted Critical
Publication of US3085982A publication Critical patent/US3085982A/en
Priority to GB39183/65A priority patent/GB1091517A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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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
    • C11D3/16Organic compounds
    • C11D3/34Organic compounds containing sulfur
    • C11D3/3418Toluene -, xylene -, cumene -, benzene - or naphthalene sulfonates or sulfates
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/29Sulfates of polyoxyalkylene ethers
    • 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
    • C11D1/83Mixtures of non-ionic with anionic compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/0094High 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/75Amino oxides

Definitions

  • suds builders may require, in certain formulations, a partic- United States Patent Ofice 3,085,982 Patented Apr. 16, 1963 3,085,982 LIQUID DETERGENT COMPOSITION David C. Steer and Norman R. Smith, Cincinnati, Ohio,
  • This invention relates to liquid detergents of mediumduty and heavy-duty, sudsing type. More particularly, it relates to improved liquid detergents which contain a tertiary amine oxide surface active agent.
  • a built detergent is one which contains, in addition to the surface active agent, a soluble salt capable of sequestering calcium and magnesium ions of hard water and also capable of increasing the level of detergent effectiveness of the surface active agent.
  • Built liquid detergents have, to some extent, replaced granular built detergents for various reasons. These reasons include: complete freedom from dustiness, compact package, convenience in pouring and measuring, and simplification of manufacture.
  • the problems which have to be overcome in formulating built detergents in clear homogeneous liquid form are mainly the problems of incorporating sufficient surface active agent and builder into the same solution.
  • an anionic sulfated or sulfonated compound is ordinarily used as surface active agent, and potassium pyrophosphate is used as builder.
  • Various surface active agents, hydrotropes and solvents are employed to increase their compatibility.
  • the fact that the builder may corrode non-ferrous metals such as aluminum, may, depending on the use for which the product is intended, lead to the inclusion of sodium silicate as a corrosion inhibitor. Its presence requires that special provisions be made to keep the ingredients compatible. Limitations on the pH of the formulation or the presence of agents designed to achieve compatibility is usually required.
  • a solubilizing agent for example triamylphosphate or potassium benzene sulfonate
  • an assistant solubilizer for example ethyl alcohol or diethyleneglycol monobutyl ether
  • a particular detergent, alkyl glyceryl ether sulfonate is used together, and the assistant solubilizer is preferably included.
  • Liquid detergents generally contain one or more agents, called suds builders, to increase their sudsing.
  • Typical suds builders are coconut ethanolamide and lauryl al- In addition to being one more ingredient to be ular perfume to cover their odor.
  • Amide-type suds builders, unless purified, are often undesirably highly colored for use in liquid products. They are not considered to serve the cleaning function of a detergent.
  • An object of this invention is to provide a homogeneous built liquid detergent of improved sudsing characteristics and good detergent effectiveness.
  • a further object of this invention is to eliminate suds builders from a high sudsing liquid detergent formulation.
  • An additional object of this invention is to eliminate the need for solvent and/ or special surface active agents (alkylolamide or alkylglyceryl ether sulfonate) in a homogeneous built liquid detergent; the object of an aspect of the invention is to do so when silicate is present.
  • a detergent formulation containing: (I) from about 3% to about 10% of an aliphatic tertiary amine oxide; (2) from about 3% to about 15% of a non-soap synthetic detergent of the sulfated or sulfonated type; (.3) from about 3% to about 10% of a soluble hydrotrope; and (4) from about 10% to about 30% of a soluble pyrophosphate salt.
  • These ingredients are dissolved in an aqueous vehicle.
  • the use of the formulation makes a corrosion inhibitor desirable, from about 3.5% to about 6% of alkali metal silicate solids are dissolved in the same solution.
  • percentages refer to weight percent of the total formula unless otherwise indicated. It will be appreciated that in an aqueous system it is for the most part immaterial by which ionic salts a particular ion is introduced; for in the aqueous product there will be substantially complete and continuous exchange of ions.
  • Amine oxides are compounds of the general formula R R R N- O.
  • the arrow is a conventional representation of a semipolar bond. They are generally prepared by the direct oxidation of the appropriate tertiary amine.
  • R is a much longer chain than R and R amine oxides have surface activity.
  • R is an alkyl radical of from about 10 to about 16 carbon atoms. Desirable surface active properties are lost if R is substantially less than 10 carbon atoms, and solubility in the present formulation is too low if R is greater than 16 carbon atoms.
  • R and R are each selected from the group consisting of methyl and ethyl radicals.
  • R is a dodecyl radical or a mixture of dodecyl with de-cyl, tetradecyl and hexadecyl radicals, such that at least 50% of the radicals are dodecyl radicals.
  • a convenient source of a preferred mixture is the middle cut of coconut fatty alcohol which has the approximate chain length composition: 2%C 66%C 23%C, and 9%C R and R are preferably methyl radicals.
  • the amine oxide is used at from about 3% to about 10% of the total formula. Too little amine oxide adversely affects the performance of the formulations and too much amine oxide interferes with achieving builder and detergent in sufficient amount in a homogeneous liquid.
  • Soluble pyrophosphate salts are suitable builders in this invention. They complex the calcium and magnesium ions of hard water; and, when the calcium ions of hard Water are present in excess, have an additional water softening effect by precipitating calcium pyrophosphate. They also serve to increase the level of detergency obtainable with synthetic surface active agents. Potassium, sodium, ethanolammonium, diethanolammonium, and triethanolammonium are suitable salts of the pyrophosphate anion in the practice of this invention; potassium pyrophosphate is especially preferred.
  • the soluble salt of pyrophosphate is employed at a level of from about 10% to about 30%.
  • the pyrophosphate salts are corrosive towards aluminum. If the detergent solution is to contact this metal for prolonged periods of time, especially at elevated temperatures, a corrosion inhibitor should be desirably included. In a product designed for hand laundry of fine fabrics, it is unnecessary.
  • Soluble silicates are highly effective inhibitors and can be added to the formulas of this invention without difficulty at levels of from about 3.5% to about 6%. Potassium, or preferably sodium silicates haviug a weight ratio of Slog/M20 of from about 1.0 to about 2. 6 and preferably from about 1.6 to about 2.6 can be used. M in this ratio refers to sodium or potassium. Less than about 3.5% sodium silicate solids, although useable in the present compositions, does not provide protection against corrosion at typical use conditions, and more than about 6% sodium silicate solids is difficult to incorporate into a homogeneous liquid.
  • Suitable hydrotropes to increase the compatibility of the ingredients of the formulations of this invention are the aryl sulfonates disclosed in the hercinbefore cited patents. More specifically they are soluble salts of the hydrotrope anions.
  • Preferred hydrotrope anions are benzene sulfonate, xylene sulfonate and toluene sulfonate. They are used as the soluble salts such as: ethanolammonium, diethanolammonium, and triethanolammonium and especially as the alkali metal, potassium, or sodium, salts. Sodium or potassium toluene sulfonate is especially preferred.
  • the hydrotrope salt is added at levels of from about 3% to about 10%.
  • Levels of from about 4% to about 6% are preferred.
  • the upper limit of about 10% is set by increasing dilution of the product by an ingredient substantially inert so far as sudsing and detergency are concerned.
  • the lower limit is the amount required to achieve a homogeneous solution. It will be appreciated that it is necessary that the formulations of this invention should be liquid at somewhat higher and at somewhat lower tem peratures than usual room temperature.
  • the amount of hydrotrope salt used is preferably the minimum amount which will hold the ingredients in solution at the temperature to which it is desired that the formula can be cooled without phase separation.
  • Amine oxide is an effective detergent; however, in order to achieve the objects of this invention, a supplemental non-soap anionic synthetic detergent is added. From about 3% to about 15% anionic detergent is employed.
  • Preferred anionic detergents which can be included are: alkyl benzene sulfonate, alkyl ethylene oxide ether sulfate wherein there are from 1 to ethylene oxide residues per alkyl and the mixtures formed when 1 to 5 ethylene oxides are reacted with one mole of alcohol, and alkyl sulfate. These may be represented, respectively, as:
  • alkyl chain (R) will contain from about 9 to about 16 carbon atoms and preferably about 12 carbon atoms.
  • Mixtures of alkyl radicals of different chain lengths are preferably used since they are soluble and readily available from synthetic or natural sources, e.g., coconut alcohol and a mixture containing tri-, tetra-, and pentapolypropylene polymers and averaging about 12 carbon atoms.
  • These detergents are used as soluble salts; specifically, they are used as sodium, potassium, ethanolammonium, diethanolammonium and triethanolammonium salts. Sodium and triethanolamine salts are preferred.
  • non-soap anionic synthetic detergents with alkyl radicals as specified above, can be usefully employed if they have the following characteristics: their salts, as specified above, are soluble to the extent of at least 3% in an aqueous solution of 3% dimethyldodecylamine oxide, 3% potassium toluene sulfonate and potassium pyrophosphate; and they are stable against hydrolysis in alkaline solution.
  • their salts as specified above, are soluble to the extent of at least 3% in an aqueous solution of 3% dimethyldodecylamine oxide, 3% potassium toluene sulfonate and potassium pyrophosphate; and they are stable against hydrolysis in alkaline solution.
  • An example is the potassium salt of the sulfated condensation product of four moles of ethylene oxide with a mole of nonyl phenol.
  • the formulas of this invention containing amine oxide, suds so well in the laundry and dishpan that no suds builder is required.
  • the alkyl sulfate makes a particular contribution to sudsing in the formulas of this invention.
  • Alkyl benzene sulfonate is particularly favored for this purpose because in most circumstances it reduces the cost of the formula.
  • a supplemental anionic detergent can tend to improve the mildness of the formulations, alkyl benzene sulfonate being particularly noteworthy in this respect.
  • the supplemental anionic detergents also permit the achieving of higher levels of active ingredients in a homogeneous liquid.
  • Alkyl benzene sulfonate and alkyl sulfate are therefore especially preferred anionic detergents.
  • Preferred formulas of this invention include those in which two anionic detergents are used in combination with the amine oxide.
  • C alkyl benzene sulfonate, coconut alkyl sulfate and dimethyldodecylarnine oxide in approximately equal quantities in a detergent combination which gives superior sudsing. good mildness to the skin and relatively low cost and is especially preferred in the practice of this invention.
  • Slight variations from equal quantities of the amine oxide and the anionic detergents permits fine adjustment of the properties of the formulas. If more of one detergent is used, preferably less of another is used.
  • the sum of anionic detergent and amine oxide is preferably kept in the range of from about 10% to about 25%.
  • the inorganic builder content is preferably raised as the total synthetic detergent content is lowered; so that the sum of builder and detergent is kept from about 25% to about 40%.
  • the product has particularly good performance and homogeneous character.
  • the product is of medium-duty type and can be recommended for hand laundering of fine fabrics and dishwashing.
  • the detergent level is lowcr or equal to the builder, the product is of heavy-duty type especially adapted for laundry and general purpose use. Silicate is particularly desirable in the heavy-duty product.
  • a soluble sodium carboxymethylcellulose may be added in amounts up to about 2% to inhibit soil redeposition.
  • a tarnish inhibitor such as benzotriazole or ethylenethiourea may be added in amounts up to about Fluorescers, perfume, and color, while not essential in the compositions of the invention, may be added in amounts less than about 1%.
  • the mole ratio of potassium (and any alkanolammonium ions) to sodium is maintained above about 3:1 to maintain the one-phase nature of the product and preferably is maintained above about 3.511.
  • Example I The following compositions were prepared and examined. All were clear homogeneous pourable liquids at room temperature. Formulas B and C were cooled to lower temperatures and remained clear at 50 F.
  • Sodium polypropylene benzene sulfonate (a mixture. of tri-, tetrm, and Terminapropylenit averaging about C12 ⁇ percent" 4 ti 3 5 Sodium coconut sulfate. .do 4 2 3 4 4 8 Potassiutntoluencsulfunate do. 6 7 G t, 6 (I lotassiumpyrophosphate lo. 15 18 18 ltt 18 Sodium silicate solids S5102:
  • composition G was prepared as a duplicate of F except the 8% sodium coconut sulfate was replaced by 6% potassium salt of a sulfated condensation product of one mole coconut 1 alcohol with 3 moles of 1 Coconut refers to the alkyls of middle out coconut alcohol containing about 2%Cio, 66%Ci2, 23%'C14. and 9%Cld. ethylene oxide. The K/ Na mole ratio in this product was about 7.4.
  • Products A, C, D, and F proved to be superior in maintaining suds during the washing of soiled dishes to com- 10 suddenly available built liquid detergents tested under the same conditions.
  • Products B and G proved to be good dishwashing products, being about equal to available built liquid products.
  • Products B and C were also employed in washing soiled clothes in a typical domestic washing machine.
  • the suds in the first load was higher than for commercial built liquid detergents tested under the same conditions.
  • the sodium silicate can be omitted from these formulas without substantially affecting appearance or performance except for their corrosiveness to non-ferrous metals.
  • Dodecyl radicals and coconut radicals are substantially equivalent, that is one can be substituted for the other in the ingredients of this example with no substantial change in appearance or performance of the product.
  • Potassium benzene sulfonate or potassium xylene sulfonate can be used to replace potassium toluene sulfonate without losing the homogeneous nature of the product or adversely affecting its performance.
  • Example I The following composition was prepared. It was a clear homogeneous pourable liquid at room temperature. It remained clear at 30 F.
  • Triethanolamine salt of polypropylene benzene sulfonate (a mixture of tri-, tetra-, and pentapropylene averaging about C 6 Potassium pyrophosphate 25 Potassium toluene sulfonate 8.5 Sodium silicate solids, Si0 to Na O is 1.6 5 Water Balance K-l-triethanolammonium/Na, approx. mole ratio 5.5
  • the suds during washing soiled dishes obtained from this product were more stable than suds obtained from commercially available built liquid detergents. This product showed good sudsing and cleaning characteristics in washing soiled clothing.
  • Example 111 The following compositions were prepared. They were clear homogeneous pourable liquids at room temperature. After freezing at 40 F. they again became clear and homogeneous on being warmed to room temperature.
  • i (oconut refers to the alkyls of middle out coconut alcohol containing about 2G1t, 6651-0 2, 237 -014, and9%C for the purposes for which medium-built liquid products are intended.
  • methylethylcoconutamine oxide or diethylcoconutamine oxide can be substituted for dimethylcoconutamine oxide without substantially adversely affecting the physical characteristics or performance of the compositions.
  • a substantially clear, high-sudsing, concentrated liquid detergent composition consisting essentially of:
  • a non-soap detergent selected from the salts of the group of detergent anions consisting of R R(OC H SO where x is an integer from 1 to 5 R being an alkyl radical containing about 9 to about 16 carbon atoms, and mixtures thereof;
  • a substantially clear high sudsing concentrated liquid detergent composition consisting essentially of:
  • a non-soap detergent selected from the salts of the group of detergent anions consisting of R80 R(OC H SO where x is an integer from I to 5 R being an alkyl radical containing about 9 to about 16 carbon atoms, and mixtures thereof;
  • liquid detergent composition of claim 3 wherein the detergent anion is a mixture of R -s Os-and R s or R being an alkyl radical containing from about 9 to about 16 carbon atoms.
  • a substantially clear high-sudsing liquid detergent composition consisting essentially of:

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  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Detergent Compositions (AREA)
US808022A 1959-04-22 1959-04-22 Liquid detergent composition Expired - Lifetime US3085982A (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
NL250715D NL250715A (xx) 1959-04-22
BE622462D BE622462A (xx) 1959-04-22
DENDAT1185756D DE1185756B (xx) 1959-04-22
US808022A US3085982A (en) 1959-04-22 1959-04-22 Liquid detergent composition
FR824805A FR1295354A (fr) 1959-04-22 1960-04-20 Compositions détersives liquides concentrées, sensiblement limpides à action moyenne ou intense
GB14304/60A GB951930A (en) 1959-04-22 1960-04-22 Liquid detergent composition
GB39183/65A GB1091517A (en) 1959-04-22 1965-09-14 Liquid detergent composition

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US808022A US3085982A (en) 1959-04-22 1959-04-22 Liquid detergent composition
GB39183/65A GB1091517A (en) 1959-04-22 1965-09-14 Liquid detergent composition

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US3085982A true US3085982A (en) 1963-04-16

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US808022A Expired - Lifetime US3085982A (en) 1959-04-22 1959-04-22 Liquid detergent composition

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US (1) US3085982A (xx)
BE (1) BE622462A (xx)
DE (1) DE1185756B (xx)
GB (2) GB951930A (xx)
NL (1) NL250715A (xx)

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3192166A (en) * 1960-11-14 1965-06-29 Procter & Gamble Liquid detergent composition
US3194767A (en) * 1961-12-18 1965-07-13 Procter & Gamble Sudsing detergent composition
US3234139A (en) * 1961-12-21 1966-02-08 Procter & Gamble Diamine dioxide detergent compositions
US3281368A (en) * 1961-12-04 1966-10-25 Procter & Gamble Built tertiary amine oxide detergents
US3296145A (en) * 1965-10-21 1967-01-03 Millmaster Onyx Corp Quaternary ammonium-tertiary amine oxide compositions
US3320078A (en) * 1965-01-18 1967-05-16 Archer Daniels Midland Co Process for insolubilizing protein
US3330327A (en) * 1964-03-30 1967-07-11 Continental Oil Co Drying tertiary amine oxides on extended heated surfaces at elevated temperatures
US3400198A (en) * 1963-08-28 1968-09-03 Procter & Gamble Wave set retention shampoo containing polyethylenimine polymers
US3527707A (en) * 1963-06-05 1970-09-08 Exxon Research Engineering Co Liquid detergent composition
US4018720A (en) * 1975-07-14 1977-04-19 The Procter & Gamble Company Laundry detergent compositions in emulsion/suspension
US4024078A (en) * 1975-03-31 1977-05-17 The Procter & Gamble Company Liquid detergent composition
US4284532A (en) * 1979-10-11 1981-08-18 The Procter & Gamble Company Stable liquid detergent compositions
US4304680A (en) * 1973-02-05 1981-12-08 Colgate-Palmolive Company Laundry soap
US4539133A (en) * 1983-03-02 1985-09-03 Lever Brothers Company Process for preparation of an anti-corrosive aqueous liquid detergent composition
US5399285A (en) * 1992-10-30 1995-03-21 Diversey Corporation Non-chlorinated low alkalinity high retention cleaners

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS51109002A (en) 1975-03-20 1976-09-27 Kao Corp Senjozaisoseibutsu
JPS5655499A (en) * 1979-10-11 1981-05-16 Lion Corp Manufacture of liquid detergent composition
US4436653A (en) 1981-04-06 1984-03-13 The Procter & Gamble Company Stable liquid detergent compositions
GR76044B (xx) * 1981-04-06 1984-08-03 Procter & Gamble
US4438024A (en) 1982-05-10 1984-03-20 The Procter & Gamble Company Stable liquid detergent compositions

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB437566A (en) * 1934-02-16 1935-10-31 Chem Ind Basel Manufacture of textile assistants
US2060568A (en) * 1934-06-23 1936-11-10 Soc Of Chemical Ind Assisting agents for the textile industry
US2169976A (en) * 1934-01-26 1939-08-15 Ig Farbenindustrie Ag Process of producing assistants in the textile and related industries
US2581677A (en) * 1952-01-08 Phosphate detergent composition in
US2877186A (en) * 1956-06-29 1959-03-10 Procter & Gamble Liquid detergent composition

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2581677A (en) * 1952-01-08 Phosphate detergent composition in
US2169976A (en) * 1934-01-26 1939-08-15 Ig Farbenindustrie Ag Process of producing assistants in the textile and related industries
GB437566A (en) * 1934-02-16 1935-10-31 Chem Ind Basel Manufacture of textile assistants
US2060568A (en) * 1934-06-23 1936-11-10 Soc Of Chemical Ind Assisting agents for the textile industry
US2877186A (en) * 1956-06-29 1959-03-10 Procter & Gamble Liquid detergent composition

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3192166A (en) * 1960-11-14 1965-06-29 Procter & Gamble Liquid detergent composition
US3281368A (en) * 1961-12-04 1966-10-25 Procter & Gamble Built tertiary amine oxide detergents
US3194767A (en) * 1961-12-18 1965-07-13 Procter & Gamble Sudsing detergent composition
US3234139A (en) * 1961-12-21 1966-02-08 Procter & Gamble Diamine dioxide detergent compositions
US3527707A (en) * 1963-06-05 1970-09-08 Exxon Research Engineering Co Liquid detergent composition
US3400198A (en) * 1963-08-28 1968-09-03 Procter & Gamble Wave set retention shampoo containing polyethylenimine polymers
US3330327A (en) * 1964-03-30 1967-07-11 Continental Oil Co Drying tertiary amine oxides on extended heated surfaces at elevated temperatures
US3320078A (en) * 1965-01-18 1967-05-16 Archer Daniels Midland Co Process for insolubilizing protein
US3296145A (en) * 1965-10-21 1967-01-03 Millmaster Onyx Corp Quaternary ammonium-tertiary amine oxide compositions
US4304680A (en) * 1973-02-05 1981-12-08 Colgate-Palmolive Company Laundry soap
US4024078A (en) * 1975-03-31 1977-05-17 The Procter & Gamble Company Liquid detergent composition
US4018720A (en) * 1975-07-14 1977-04-19 The Procter & Gamble Company Laundry detergent compositions in emulsion/suspension
US4284532A (en) * 1979-10-11 1981-08-18 The Procter & Gamble Company Stable liquid detergent compositions
US4539133A (en) * 1983-03-02 1985-09-03 Lever Brothers Company Process for preparation of an anti-corrosive aqueous liquid detergent composition
US5399285A (en) * 1992-10-30 1995-03-21 Diversey Corporation Non-chlorinated low alkalinity high retention cleaners

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Publication number Publication date
GB951930A (en) 1964-03-11
DE1185756B (xx)
GB1091517A (en) 1967-11-15
BE622462A (xx)
NL250715A (xx)

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