EP0206375A1 - Liquid cleaning and softening compositions - Google Patents

Liquid cleaning and softening compositions Download PDF

Info

Publication number
EP0206375A1
EP0206375A1 EP86200859A EP86200859A EP0206375A1 EP 0206375 A1 EP0206375 A1 EP 0206375A1 EP 86200859 A EP86200859 A EP 86200859A EP 86200859 A EP86200859 A EP 86200859A EP 0206375 A1 EP0206375 A1 EP 0206375A1
Authority
EP
European Patent Office
Prior art keywords
amine
composition according
component
weight
composition
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP86200859A
Other languages
German (de)
French (fr)
Other versions
EP0206375B1 (en
Inventor
Tan Tai Dr. Ho
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Unilever PLC
Unilever NV
Original Assignee
Unilever PLC
Unilever NV
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from GB858513421A external-priority patent/GB8513421D0/en
Priority claimed from GB858514583A external-priority patent/GB8514583D0/en
Application filed by Unilever PLC, Unilever NV filed Critical Unilever PLC
Publication of EP0206375A1 publication Critical patent/EP0206375A1/en
Application granted granted Critical
Publication of EP0206375B1 publication Critical patent/EP0206375B1/en
Expired legal-status Critical Current

Links

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
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/40Monoamines or polyamines; Salts thereof
    • 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
    • C11D10/00Compositions of detergents, not provided for by one single preceding group
    • C11D10/04Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
    • 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
    • C11D3/001Softening compositions
    • C11D3/0015Softening compositions liquid
    • 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
    • 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
    • C11D1/22Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic 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
    • 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
    • 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
    • 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

Definitions

  • the present invention relates to aqueous liquid detergent compositions of the suspending type, i.e. compositions in which particles of a different density can be stably suspended.
  • the invention relates to aqueous liquid detergent compositions of the suspending type which exhibit good cleaning performance and simultaneously impart a softening quality to the fabrics being laundered.
  • Simultaneous cleaning and softening is desirable, as it provides the user with increased convenience in the laundering operation, rendering redundant the after-wash softening/rinse cycle and the separate dosing of special-purpose softening compositions.
  • long-chain fatty amines which are suitable to impart through-the-wash softening, can be stably incorporated in aqueous suspending liquid detergent compositions at a pH equal to or below the isoelectric point of the amine without adverse effect on the suspending properties of the composition if a hydrotropic agent is included in an amount which will be defined hereunder more precisely.
  • an aqueous suspending liquid detergent composition for the cleaning and softening of fabrics which comprises:
  • composition also comprises one or more electrolytes as part of the active system, thereby providing the structure necessary for the suspending properties of the composition.
  • Suitable nonionic detergent-actives for use in the present invention may be found in the following classes: fatty acid alkylolamides, alkylene oxide condensates of alkylphenols or primary and secondary aliphatic alcohols, alkylamines, alkyl mercaptans and amine oxides.
  • ethylene oxide condensates and mixtures of ethylene oxide condensates with fatty acid alkylolamides are preferred. Particularly suitable have been found ethylene oxides having a hydrophilic-lipophilic balance of between 11 and 15, such as C " -C, 5 alcohols condensed with 6-8 ethylene oxides.
  • anionic derivatives of, in particular, polyalkoxylated nonionic detergent materials which have retained to a large extent a nonionic character can be used instead of or in combination with nonionic detergent-actives.
  • Suitable examples are the sulphated, phosphated or carboxylated polyalkoxylated nonionic detergent-actives, such as the alkyl and arkylaryl polyethoxy ether sulphates.
  • Suitable alkyl polyethoxy ether sulphates have about 10 to about 18 carbon atoms in the alkyl chain and have an average of 1 to 12, preferably 1 to 6 ethylene oxide units.
  • anionic surfactants can be used in the compositions of the present invention.
  • Suitable anionic non-soap surfactants are water-soluble salts of alkyl benzene sulphonates, alkyl sulphates, paraffin sulphonates,alpha-olefin sulphonates, alpha-sulphocarboxylates and their esters, alkyl glyceryl ether sulphonates, fatty acid monoglyceride sulphates and sulphonates, 2- acyloxy-alkane-1-sulphonates, and beta-alkoxy alkane sulphonates. Soaps are also suitable anionic surfactants.
  • Especially preferred alkyl benzene sulphonates have about 9 to about 15 carbon atoms in a linear or branched alkyl chain, more especially about 11 to about 13 carbon atoms.
  • Suitable alkyl sulphates have about 10 to about 22 carbon atoms in the alkyl chain, more especially from about 12 to about 18 carbon atoms.
  • Suitable paraffin sulphonates are essentially linear and contain from about 8 to about 24 carbon atoms, more especially from about 14 to about 18 carbon atoms.
  • Suitable alpha-olefin sulphonates have about 10 to about 24 carbon atoms, more especially about 14 to about 16 carbon atoms; alpha-olefin sulphonates can be made by reaction with sulphur trioxide, followed by neutralization under conditions such that any sultones present are hydrolyzed to the corresponding hydroxy alkane sulphonates.
  • Suitable alpha-sulphocarboxylates contain from about 6 to about 20 carbon atoms; included herein are not only the salts of alpha- sulphonated fatty acids, but also their esters made from alcohols containing about 1 to about 14 carbon atoms.
  • Suitable alkyl glyceryl ether sulphates are ethers of alcohols having about 10 to about 18 carbon atoms, more especially those derived from coconut oil and tallow.
  • Suitable alkyl phenol polyethoxy ether sulphates have about 8 to about 12 carbon atoms in the alkyl chain and an average of about 1 to about 6 ethylene oxide units per molecule.
  • Suitable 2-acyloxy-alkane-1-sulphonates contain from about 2 to about 9 carbon atoms in the acyl group and about 9 to about 23 carbon atoms in the alkane moiety.
  • Suitable beta-alkyloxy alkane sulphonates contain about 1 to about 3 carbon atoms in the alkyl group and about 8 to about 20 carbon atoms in the alkane moiety.
  • the alkyl chains of the foregoing non-soap anionic surfactants can be derived from natural sources such as coconut oil or tallow, or can be made synthetically, as for example by using the Ziegler or Oxo processes. Water-solubility can be achieved by using alkali metal, ammonium, or alkanolammonium cations; sodium is preferred. Mixtures of anionic surfactants are contemplated by this invention; a satisfactory mixture contains alkyl benzene sulphonate having 11-13 carbon atoms in the alkyl group and alkyl sulphate having 12 to 18 carbon atoms in the alkyl group.
  • Suitable soaps contain about 8 to about 18 carbon atoms, more especially about 12 to about 18 carbon atoms.
  • Soaps can be made by direct saponification of natural fats and oils such as coconut oil, tallow and palm oil, or by neutralization of free fatty acids obtained from either natural or synthetic sources.
  • the soap cation can be alkali metal, ammonium or alkanolammonium; sodium is preferred.
  • the amount of the active detergent material may vary from 1 to 60%, preferably from 2-40% and especially preferably from 5-25%; when mixtures of e.g. anionics and nonionics are used, the relative weight ratio varies from 10:1 to 1:10, preferably from 6:1 to 1:6. When a soap is also incorporated, the amount thereof is from 1-40% by weight.
  • a particularly preferred active detergent mixture is that of a water-soluble anionic sulphonate or sulphate detergent and a nonionic detergent in a weight ratio of from about 6:1 to 1:1, with or without a soap in a ratio of up to 2:1 with respect to the nonionic detergent constituent.
  • the inclusion of one or more electrolytes, in particular of the salting-out type, is often essential.
  • the composition may contain from 1 to 60% by weight, and preferably from 3 to 50% by weight, and particularly preferably from 10 to 35% by weight of the salting-out electrolytes.
  • Typical examples of such salting-out electrolytes are water-soluble builder salts, such as the alkali metal ortho-and pyrophosphates, the alkali metal tripolyphosphates, such as sodium tripolyphosphate, the alkali metal silicates, alkali metal borates, alkali metal carbonates, alkali metal sulphates, alkali metal citrates; alkali metal salts of nitrilotriacetate; alkali metal salts of carbox- ymethyloxy succinate.
  • the alkali metal salts the ammonium and ethanol-substituted ammonium salts can be used.
  • may be advantageous to include also a certain level of a non-salting-out electrolyte. This can be determined by routine experimentation, using the general indications below as to level and type of auxiliary electrolytes.
  • auxiliary electrolytes are alkali metal iodides, alkali metal (per)-chlorates, alkali metal rhodanides, and alkali metal nitrates, and alkali metal bromides and alkali metal chlorides.
  • the corresponding ammonium and ethanol-substituted ammonium salts can also be used.
  • the auxiliary electrolyte is generally used in the composition in an amount of 0.5 to 35% by weight, preferably 1 to 30% by weight, and particularly preferably 2 to 25% by weight.
  • Long-chain fatty amines suitable for the purpose of the invention are substantially water-insoluble compounds that have the general formula:
  • compositions should contain from 0.5% to 15% by weight of the amine, preferably from 1% to 10% by weight and most preferably from 2% to 5% by weight.
  • the hydrotropic agent is the hydrotropic agent
  • An essential aspect of the present invention is the inclusion of a hydrotropic agent. It has been found that such inclusion compensates the normally adverse effect on stability due to the incorporation of the at least partially charged amines.
  • Suitable hydrotropic agents for use in the present invention are those conventionally used for this purpose in the art. Suitable examples are the water-soluble organic solvents such as the lower alcohols, diols and triols, water-soluble organic compounds such as urea, the short alkyl chain aromatic sulphonic acid salts such as sodium toluene sulphonate and sodium xylene sulphonate.
  • water-soluble organic solvents such as the lower alcohols, diols and triols
  • water-soluble organic compounds such as urea
  • the short alkyl chain aromatic sulphonic acid salts such as sodium toluene sulphonate and sodium xylene sulphonate.
  • the group of the short alkyl chain aromatic sulphonates is preferred.
  • the optimal amount of the hydrotropic agent depends on the type and concentration of the fatty amine, and can be simply determined by standard routines used in the art. In general, the hydrotropic agent is included in an amount of 1 to 10% by weight.
  • the pH of the composition is such that the fatty amine is at least partially protonated, and therefore is equal to or below the isoelectric point of the amine.
  • the isoelectric point of any given amine can be determined by measuring the electrophoretic mobility of an aqueous dispersion of the amine under standard conditions of concentration and temperature at a series of pHs, with plotting of the mobilities against pH to determine the pH of zero mobility.
  • T and Co represent the mixed alkyl radical derived from hydrogenated tallow acid and coconut oil acid, respectively.
  • the liquid detergent composition of the invention may further contain any of the adjuncts normally used in fabric-washing detergent compositions, e.g. sequestering agents such as ethylene diamine tetraacetate; alkali silicates for adjusting the pH; soil-suspending and anti-redeposition agents such as sodium carboxymethylcellulose, polyvinylpyrrolidone, etc.; fluorescent agents; perfumes, germicides and colourants.
  • adjuncts normally used in fabric-washing detergent compositions e.g. sequestering agents such as ethylene diamine tetraacetate; alkali silicates for adjusting the pH; soil-suspending and anti-redeposition agents such as sodium carboxymethylcellulose, polyvinylpyrrolidone, etc.; fluorescent agents; perfumes, germicides and colourants.
  • lather depressors such as silicones; and enzymes, particularly proteolytic and amylolytic enzymes; and peroxygen or chlorine bleaches, such as sodium perborate and potassium dichlorocyanurate, including bleach activators, such as N,N,N',N'-tetraacetylethylenediamine, may be necessary to formulate a complete heavy duty detergent compositions suitable for use in washing machine operations.
  • lather depressors such as silicones
  • enzymes particularly proteolytic and amylolytic enzymes
  • peroxygen or chlorine bleaches such as sodium perborate and potassium dichlorocyanurate
  • bleach activators such as N,N,N',N'-tetraacetylethylenediamine
  • the composition of the invention has a viscosity of up to 1.2 Pas, and most preferably from 0.4 to 1.0 Pas as measured at 20°C and at a shear rate of 21 seconds-'.

Landscapes

  • Chemical & Material Sciences (AREA)
  • 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)

Abstract

Aqueous liquid detergent composition for simultaneous cleaning and softening of fabrics comprising a binary active suspending system, a long-chain fatty amine as softening agent and from 1 to 10% of a hydrotrope, the pH of the composition being below the isoelectric point of the amine component. A stable suspending composition is achieved delivering good cleaning and softening performance.

Description

  • The present invention relates to aqueous liquid detergent compositions of the suspending type, i.e. compositions in which particles of a different density can be stably suspended. In particular, the invention relates to aqueous liquid detergent compositions of the suspending type which exhibit good cleaning performance and simultaneously impart a softening quality to the fabrics being laundered.
  • Simultaneous cleaning and softening is desirable, as it provides the user with increased convenience in the laundering operation, rendering redundant the after-wash softening/rinse cycle and the separate dosing of special-purpose softening compositions.
  • A number of attempts have been made to formulate fabric-washing detergent compositions which exhibit the cleaning performance as expected by the modem user and simultaneously provide sufficient softening efficacy. In the field of solid detergent compositions, proposals have been made to incorporate cationic fabric softeners in anionic detergent-based compositions by inclusion of means which overcome the natural incompatibility of anionic and cationic detergent actives due to complexation of these compounds resulting in a consequent decrease in detergency and softening efficacy.
  • To our knowledge, no proposals have been made to formulate aqueous liquid compositions based on structured active systems including a combination of anionic and cationic detergent actives.
  • Surprisingly, it has now been found that long-chain fatty amines, which are suitable to impart through-the-wash softening, can be stably incorporated in aqueous suspending liquid detergent compositions at a pH equal to or below the isoelectric point of the amine without adverse effect on the suspending properties of the composition if a hydrotropic agent is included in an amount which will be defined hereunder more precisely.
  • Accordingly, the present invention provides an aqueous suspending liquid detergent composition for the cleaning and softening of fabrics which comprises:
    • (a) a nonionic detergent-active material and/or an anionic derivative of a polyalkoxylated nonionic detergent-active material; and
    • (b) an anionic detergent-active material other than component (a),

    characterized in that it further comprises:
    • (c) an effective amount of a long-chain fatty amine; and
    • (d) 1-10% by weight of a hydrotropic agent;

    the pH of said composition being equal to or below the isoelectric point of said amine.
  • In general the composition also comprises one or more electrolytes as part of the active system, thereby providing the structure necessary for the suspending properties of the composition.
  • The invention will now be discussed in more detail.
  • The nonionic detergent-active material
  • Suitable nonionic detergent-actives for use in the present invention may be found in the following classes: fatty acid alkylolamides, alkylene oxide condensates of alkylphenols or primary and secondary aliphatic alcohols, alkylamines, alkyl mercaptans and amine oxides.
  • The ethylene oxide condensates and mixtures of ethylene oxide condensates with fatty acid alkylolamides are preferred. Particularly suitable have been found ethylene oxides having a hydrophilic-lipophilic balance of between 11 and 15, such as C"-C,5 alcohols condensed with 6-8 ethylene oxides.
  • Also anionic derivatives of, in particular, polyalkoxylated nonionic detergent materials which have retained to a large extent a nonionic character, can be used instead of or in combination with nonionic detergent-actives. Suitable examples are the sulphated, phosphated or carboxylated polyalkoxylated nonionic detergent-actives, such as the alkyl and arkylaryl polyethoxy ether sulphates. Suitable alkyl polyethoxy ether sulphates have about 10 to about 18 carbon atoms in the alkyl chain and have an average of 1 to 12, preferably 1 to 6 ethylene oxide units.
  • The anionic detergent-active material
  • A wide range of anionic surfactants can be used in the compositions of the present invention.
  • Suitable anionic non-soap surfactants are water-soluble salts of alkyl benzene sulphonates, alkyl sulphates, paraffin sulphonates,alpha-olefin sulphonates, alpha-sulphocarboxylates and their esters, alkyl glyceryl ether sulphonates, fatty acid monoglyceride sulphates and sulphonates, 2- acyloxy-alkane-1-sulphonates, and beta-alkoxy alkane sulphonates. Soaps are also suitable anionic surfactants.
  • Especially preferred alkyl benzene sulphonates have about 9 to about 15 carbon atoms in a linear or branched alkyl chain, more especially about 11 to about 13 carbon atoms. Suitable alkyl sulphates have about 10 to about 22 carbon atoms in the alkyl chain, more especially from about 12 to about 18 carbon atoms.
  • Suitable paraffin sulphonates are essentially linear and contain from about 8 to about 24 carbon atoms, more especially from about 14 to about 18 carbon atoms. Suitable alpha-olefin sulphonates have about 10 to about 24 carbon atoms, more especially about 14 to about 16 carbon atoms; alpha-olefin sulphonates can be made by reaction with sulphur trioxide, followed by neutralization under conditions such that any sultones present are hydrolyzed to the corresponding hydroxy alkane sulphonates. Suitable alpha-sulphocarboxylates contain from about 6 to about 20 carbon atoms; included herein are not only the salts of alpha- sulphonated fatty acids, but also their esters made from alcohols containing about 1 to about 14 carbon atoms.
  • Suitable alkyl glyceryl ether sulphates are ethers of alcohols having about 10 to about 18 carbon atoms, more especially those derived from coconut oil and tallow. Suitable alkyl phenol polyethoxy ether sulphates have about 8 to about 12 carbon atoms in the alkyl chain and an average of about 1 to about 6 ethylene oxide units per molecule. Suitable 2-acyloxy-alkane-1-sulphonates contain from about 2 to about 9 carbon atoms in the acyl group and about 9 to about 23 carbon atoms in the alkane moiety. Suitable beta-alkyloxy alkane sulphonates contain about 1 to about 3 carbon atoms in the alkyl group and about 8 to about 20 carbon atoms in the alkane moiety.
  • The alkyl chains of the foregoing non-soap anionic surfactants can be derived from natural sources such as coconut oil or tallow, or can be made synthetically, as for example by using the Ziegler or Oxo processes. Water-solubility can be achieved by using alkali metal, ammonium, or alkanolammonium cations; sodium is preferred. Mixtures of anionic surfactants are contemplated by this invention; a satisfactory mixture contains alkyl benzene sulphonate having 11-13 carbon atoms in the alkyl group and alkyl sulphate having 12 to 18 carbon atoms in the alkyl group.
  • Suitable soaps contain about 8 to about 18 carbon atoms, more especially about 12 to about 18 carbon atoms. Soaps can be made by direct saponification of natural fats and oils such as coconut oil, tallow and palm oil, or by neutralization of free fatty acids obtained from either natural or synthetic sources. The soap cation can be alkali metal, ammonium or alkanolammonium; sodium is preferred.
  • The amount of the active detergent material may vary from 1 to 60%, preferably from 2-40% and especially preferably from 5-25%; when mixtures of e.g. anionics and nonionics are used, the relative weight ratio varies from 10:1 to 1:10, preferably from 6:1 to 1:6. When a soap is also incorporated, the amount thereof is from 1-40% by weight.
  • A particularly preferred active detergent mixture is that of a water-soluble anionic sulphonate or sulphate detergent and a nonionic detergent in a weight ratio of from about 6:1 to 1:1, with or without a soap in a ratio of up to 2:1 with respect to the nonionic detergent constituent.
  • The electrolytes
  • In order to establish the suspending properties of the compositions according to the present invention, the inclusion of one or more electrolytes, in particular of the salting-out type, is often essential.
  • It is well known that the extent to which a nonionic detergent-active or derivative thereof is salted out by a salting-out electrolyte, resulting in a certain lowering of the cloud point, is dependent upon the nature and the amount of salting-out electrolyte used. In general, the composition may contain from 1 to 60% by weight, and preferably from 3 to 50% by weight, and particularly preferably from 10 to 35% by weight of the salting-out electrolytes.
  • Typical examples of such salting-out electrolytes are water-soluble builder salts, such as the alkali metal ortho-and pyrophosphates, the alkali metal tripolyphosphates, such as sodium tripolyphosphate, the alkali metal silicates, alkali metal borates, alkali metal carbonates, alkali metal sulphates, alkali metal citrates; alkali metal salts of nitrilotriacetate; alkali metal salts of carbox- ymethyloxy succinate. instead of the alkali metal salts, the ammonium and ethanol-substituted ammonium salts can be used.
  • Depending upon type and level of salting-out electrolyte used, it may be advantageous to include also a certain level of a non-salting-out electrolyte. This can be determined by routine experimentation, using the general indications below as to level and type of auxiliary electrolytes.
  • Typical examples of suitable auxiliary electrolytes are alkali metal iodides, alkali metal (per)-chlorates, alkali metal rhodanides, and alkali metal nitrates, and alkali metal bromides and alkali metal chlorides. The corresponding ammonium and ethanol-substituted ammonium salts can also be used. The auxiliary electrolyte is generally used in the composition in an amount of 0.5 to 35% by weight, preferably 1 to 30% by weight, and particularly preferably 2 to 25% by weight.
  • The long-chain fatty amine
  • Long-chain fatty amines suitable for the purpose of the invention are substantially water-insoluble compounds that have the general formula:
    Figure imgb0001
    • wherein: R, is a C10-C26 alkyl or alkenyl group,
    • R2 is H or a C1-C26 alkyl or alkenyl group, and
    • R3 is H or a C,-C, alkyl, alkenyl or alkylaryl group.
    • Preferably R3 is methyl or ethyl. Suitable amines include:
      • monotallowyl amine
      • ditallowyl amine
      • dilauryl methylamine
      • dimyristyl methylamine
      • dicetyl methylamine
      • distearyl methylamine.
  • Preferred are monotallowyl amine, ditallowyl amine and ditallowyl methylamine. These are commercially available as Armeen HT, 2HT and M2HT from Akzo N.V..
  • Mixtures of any of these amines may be used.
  • The compositions should contain from 0.5% to 15% by weight of the amine, preferably from 1% to 10% by weight and most preferably from 2% to 5% by weight.
  • The hydrotropic agent
  • An essential aspect of the present invention is the inclusion of a hydrotropic agent. It has been found that such inclusion compensates the normally adverse effect on stability due to the incorporation of the at least partially charged amines.
  • Suitable hydrotropic agents for use in the present invention are those conventionally used for this purpose in the art. Suitable examples are the water-soluble organic solvents such as the lower alcohols, diols and triols, water-soluble organic compounds such as urea, the short alkyl chain aromatic sulphonic acid salts such as sodium toluene sulphonate and sodium xylene sulphonate.
  • The group of the short alkyl chain aromatic sulphonates is preferred.
  • The optimal amount of the hydrotropic agent depends on the type and concentration of the fatty amine, and can be simply determined by standard routines used in the art. In general, the hydrotropic agent is included in an amount of 1 to 10% by weight.
  • The pH
  • The pH of the composition is such that the fatty amine is at least partially protonated, and therefore is equal to or below the isoelectric point of the amine.
  • The isoelectric point of any given amine can be determined by measuring the electrophoretic mobility of an aqueous dispersion of the amine under standard conditions of concentration and temperature at a series of pHs, with plotting of the mobilities against pH to determine the pH of zero mobility.
  • The isoelectric points of a series of amines are given in the following table, in which T and Co represent the mixed alkyl radical derived from hydrogenated tallow acid and coconut oil acid, respectively.
    • TzNH 7.4
    • T3N 8.2
    • T2NCH3 8.8
    • Co2NCH3 9.1
    • TN(CH3)2 10.0
    • THN2 10.9
    Minor ingredients
  • The liquid detergent composition of the invention may further contain any of the adjuncts normally used in fabric-washing detergent compositions, e.g. sequestering agents such as ethylene diamine tetraacetate; alkali silicates for adjusting the pH; soil-suspending and anti-redeposition agents such as sodium carboxymethylcellulose, polyvinylpyrrolidone, etc.; fluorescent agents; perfumes, germicides and colourants.
  • Further, the addition of lather depressors such as silicones; and enzymes, particularly proteolytic and amylolytic enzymes; and peroxygen or chlorine bleaches, such as sodium perborate and potassium dichlorocyanurate, including bleach activators, such as N,N,N',N'-tetraacetylethylenediamine, may be necessary to formulate a complete heavy duty detergent compositions suitable for use in washing machine operations. These ingredients can be employed in the liquid detergent compositions of the invention without the danger of undue decomposition during storage if a proper protective coating is applied.
  • Preferably the composition of the invention has a viscosity of up to 1.2 Pas, and most preferably from 0.4 to 1.0 Pas as measured at 20°C and at a shear rate of 21 seconds-'.
  • The invention will now be further illustrated by way of examples, percentages in which are by weight of the total composition unless otherwise indicated.
  • Specifications and properties of ingredients:
    • Armeen HT = primary hardened tallow amine R-NH2
    • melting range : 47-55°C
    • isoelectric pH : 10.9 M = 256
    • R : C16 = 31% C 18 = 59%
    • supplier : AKZO Chemie
    • Synperonic K87 = C13-C15 fatty alcohol condensed with 7 moles of alkylene oxide (92% ethylene oxide, 8% propylene oxide)
    • STP = Na5P3O10: Thermphos NW; ex Knapsack
    • Glycerol = C3H8O3 (86.5%), water (13.5%)
    Example
  • Figure imgb0002

Claims (10)

1. Aqueous suspending liquid detergent composition for the cleaning and softening of fabrics, comprising:
(a) a nonionic detergent-active material and/or an anionic derivative of a polyalkoxylated nonionic detergent-active material; and
(b) an anionic detergent-active material other than component (a),

characterized in that the composition further comprises:
(c) an effective amount of a long-chain fatty amine; and
(d) 1-10% by weight of a hydrotropic agent;

the pH of the composition being equal to or below the isoelectric point of said amine.
2. Composition according to claim 1, which further comprises as component (e) from 1-60% by weight of electrolytes of the salting-out type.
3. Composition according to claim 2, which comprises from 10-35% by weight of component - (e).
4. Composition according to claim 2 or 3, which further comprises as component (f) from 0.5-35% by weight of electrolytes of the non-satting-out type.
5. Composition according to any one of the preceding claims, wherein component (c) has the general formula:
Figure imgb0003
wherein R, is a C10-C25 alkenyl group,
R2 is H or a C1-C26 alkyl or alkenyl group, and
R3 is H or a C,-C, alkyl, alkenyl or alkylaryl group.
6. Composition according to claim 5, wherein R3 is methyl or ethyl.
7. Composition according to claim 5, wherein the amine is a monotallowyl amine, a ditallowyl amine or a ditallowyl methyl amine.
8. Composition according to any one of the preceding claims, which comprises from 0.5-15% by weight of component (c).
9. Composition according to any one of the preceding claims, wherein component (d) is a short alkyl chain aromatic sulphonate.
10. Composition according to any one of the preceding claims, which has a pH at which component (c) is at least partially protonated.
EP86200859A 1985-05-28 1986-05-20 Liquid cleaning and softening compositions Expired EP0206375B1 (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
GB858513421A GB8513421D0 (en) 1985-05-28 1985-05-28 Liquid cleaning & softening compositions
GB8513421 1985-05-28
GB858514583A GB8514583D0 (en) 1985-06-10 1985-06-10 Liquid cleaning & softening compositions
GB8514583 1985-06-10

Publications (2)

Publication Number Publication Date
EP0206375A1 true EP0206375A1 (en) 1986-12-30
EP0206375B1 EP0206375B1 (en) 1988-12-21

Family

ID=26289295

Family Applications (1)

Application Number Title Priority Date Filing Date
EP86200859A Expired EP0206375B1 (en) 1985-05-28 1986-05-20 Liquid cleaning and softening compositions

Country Status (3)

Country Link
EP (1) EP0206375B1 (en)
AU (1) AU579732B2 (en)
DE (1) DE3661481D1 (en)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0276501A2 (en) * 1987-01-24 1988-08-03 Akzo Nobel N.V. Thickening compositions and thickened aqueous acid solutions
EP0309264A2 (en) * 1987-09-24 1989-03-29 Unilever Plc A composition for softening fabrics
US4842771A (en) * 1986-09-29 1989-06-27 Akzo N.V. Thickened aqueous cleaning compositions
GB2222609A (en) * 1988-08-04 1990-03-14 Albright & Wilson Fabric conditioners
EP0409503A2 (en) * 1989-07-17 1991-01-23 Unilever Plc Fabric softening composition
EP0417987A2 (en) * 1989-09-11 1991-03-20 Unilever Plc Fabric softening
WO1994005754A1 (en) * 1992-09-04 1994-03-17 Henkel Kommanditgesellschaft Auf Aktien Aqueous textile softener dispersions
EP1081269A1 (en) * 1998-05-20 2001-03-07 Kao Corporation Softening finish composition
WO2002092742A1 (en) * 2001-05-11 2002-11-21 Reckitt Benckiser N.V. Fabric softening composition
US6541444B1 (en) 1998-05-20 2003-04-01 Kao Corporation Softener composition
WO2006041704A1 (en) * 2004-10-04 2006-04-20 Akzo Nobel N.V. Light duty liquid detergent composition

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2836277A1 (en) * 1977-08-22 1979-03-01 Unilever Nv METHOD FOR PRODUCING A LIQUID DETERGENT ON AQUEOUS BASE
EP0011340B1 (en) * 1978-11-20 1982-11-24 THE PROCTER & GAMBLE COMPANY Detergent composition having textile softening properties
EP0120528A1 (en) * 1983-03-10 1984-10-03 Unilever N.V. Detergent compositions

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2648304A1 (en) * 1975-10-31 1977-05-05 Procter & Gamble Europ LIQUID DETERGENT

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2836277A1 (en) * 1977-08-22 1979-03-01 Unilever Nv METHOD FOR PRODUCING A LIQUID DETERGENT ON AQUEOUS BASE
EP0011340B1 (en) * 1978-11-20 1982-11-24 THE PROCTER & GAMBLE COMPANY Detergent composition having textile softening properties
EP0120528A1 (en) * 1983-03-10 1984-10-03 Unilever N.V. Detergent compositions

Cited By (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4842771A (en) * 1986-09-29 1989-06-27 Akzo N.V. Thickened aqueous cleaning compositions
US4853146A (en) * 1987-01-24 1989-08-01 Akzo N.V. Thickening compositions and thickened aqueous acid solutions
EP0276501A3 (en) * 1987-01-24 1989-08-16 Akzo N.V. Thickening compositions and thickened aqueous acid solutions
EP0276501A2 (en) * 1987-01-24 1988-08-03 Akzo Nobel N.V. Thickening compositions and thickened aqueous acid solutions
AU616204B2 (en) * 1987-09-24 1991-10-24 Unilever Plc A composition for softening fabrics
EP0309264A2 (en) * 1987-09-24 1989-03-29 Unilever Plc A composition for softening fabrics
EP0309264A3 (en) * 1987-09-24 1989-12-06 Unilever Plc A composition for softening fabrics
US4970028A (en) * 1987-09-24 1990-11-13 Lever Brothers Company Composition for softening fabrics
GB2222609A (en) * 1988-08-04 1990-03-14 Albright & Wilson Fabric conditioners
EP0409503A2 (en) * 1989-07-17 1991-01-23 Unilever Plc Fabric softening composition
EP0409503A3 (en) * 1989-07-17 1991-11-21 Unilever Plc Fabric softening composition
EP0417987A3 (en) * 1989-09-11 1991-08-14 Unilever Plc Fabric softening
EP0417987A2 (en) * 1989-09-11 1991-03-20 Unilever Plc Fabric softening
WO1994005754A1 (en) * 1992-09-04 1994-03-17 Henkel Kommanditgesellschaft Auf Aktien Aqueous textile softener dispersions
EP1081269A1 (en) * 1998-05-20 2001-03-07 Kao Corporation Softening finish composition
EP1081269A4 (en) * 1998-05-20 2002-03-27 Kao Corp Softening finish composition
US6541444B1 (en) 1998-05-20 2003-04-01 Kao Corporation Softener composition
US7351685B2 (en) 1998-05-20 2008-04-01 Kao Corporation Softener composition
WO2002092742A1 (en) * 2001-05-11 2002-11-21 Reckitt Benckiser N.V. Fabric softening composition
WO2006041704A1 (en) * 2004-10-04 2006-04-20 Akzo Nobel N.V. Light duty liquid detergent composition

Also Published As

Publication number Publication date
AU5797286A (en) 1986-12-04
DE3661481D1 (en) 1989-01-26
EP0206375B1 (en) 1988-12-21
AU579732B2 (en) 1988-12-08

Similar Documents

Publication Publication Date Title
EP0151678B1 (en) Stable liquid detergent compositions
EP0181041B1 (en) Ethanol-free liquid laundry detergent compositions
US4561998A (en) Near-neutral pH detergents containing anionic surfactant, cosurfactant and fatty acid
CA1109759A (en) Detergent compositions
EP0095205B1 (en) Fatty acid containing detergent compositions
CA1102202A (en) Granular detergent compositions for improved greasy soil removal
CA1312419C (en) Composition for softening fabrics
US4302364A (en) Liquid detergent compositions comprising anionic, nonionic and cationic surfactants
GB1514276A (en) Fabric-softening compositions
JP4063866B2 (en) Detergent composition comprising an amine and an anionic surfactant
US4714565A (en) Homogeneous concentrated liquid detergent compositions containing a monoester of a dicarboxylic acid
EP0000225A1 (en) Solid detergent composition for improved greasy soil removal
EP0206375B1 (en) Liquid cleaning and softening compositions
EP0348183A2 (en) Enzyme-containing liquid detergents
US5981466A (en) Detergent compositions containing amines and anionic surfactants
US4199483A (en) Detergent compositions containing salicylate corrosion inhibitor
IE61343B1 (en) Detergent/softening compositions containing hectorite clays
CA1239324A (en) Detergent composition containing semi-polar nonionic detergent, alkaline earth metal anionic detergent, and amidoalkylbetaine detergent
EP0241073B2 (en) Liquid detergents containing anionic surfactant, succinate builder and fatty acid
GB2169916A (en) Built liquid detergent containing anionic, ethoxylated nonionic and amide surfactants
NZ201708A (en) Low viscosity built bleaching liquid detergent compositions
EP0203660B1 (en) Liquid cleaning and softening compositions
SE449372B (en) LOW PHOSPHATE CONTENT COMPOSITION
JPH0323120B2 (en)
GB1572605A (en) Liqid enzyme containing detergent composition

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): CH DE FR GB IT LI NL SE

17P Request for examination filed

Effective date: 19861127

17Q First examination report despatched

Effective date: 19870728

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): CH DE FR GB IT LI NL SE

ITF It: translation for a ep patent filed
REF Corresponds to:

Ref document number: 3661481

Country of ref document: DE

Date of ref document: 19890126

ET Fr: translation filed
R20 Corrections of a patent specification

Effective date: 19890313

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed
PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 19930408

Year of fee payment: 8

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: SE

Payment date: 19930414

Year of fee payment: 8

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: CH

Payment date: 19930419

Year of fee payment: 8

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 19930421

Year of fee payment: 8

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 19930427

Year of fee payment: 8

ITTA It: last paid annual fee
PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 19930531

Year of fee payment: 8

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Effective date: 19940520

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Effective date: 19940521

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LI

Effective date: 19940531

Ref country code: CH

Effective date: 19940531

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Effective date: 19941201

NLV4 Nl: lapsed or anulled due to non-payment of the annual fee
GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 19940520

EUG Se: european patent has lapsed

Ref document number: 86200859.6

Effective date: 19941210

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Effective date: 19950131

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Effective date: 19950201

EUG Se: european patent has lapsed

Ref document number: 86200859.6

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES;WARNING: LAPSES OF ITALIAN PATENTS WITH EFFECTIVE DATE BEFORE 2007 MAY HAVE OCCURRED AT ANY TIME BEFORE 2007. THE CORRECT EFFECTIVE DATE MAY BE DIFFERENT FROM THE ONE RECORDED.

Effective date: 20050520