EP0336740B1 - Detergent composition - Google Patents

Detergent composition Download PDF

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Publication number
EP0336740B1
EP0336740B1 EP89303376A EP89303376A EP0336740B1 EP 0336740 B1 EP0336740 B1 EP 0336740B1 EP 89303376 A EP89303376 A EP 89303376A EP 89303376 A EP89303376 A EP 89303376A EP 0336740 B1 EP0336740 B1 EP 0336740B1
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EP
European Patent Office
Prior art keywords
detergent composition
carbon atoms
surfactant
sodium
composition according
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EP89303376A
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German (de)
French (fr)
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EP0336740A2 (en
EP0336740A3 (en
Inventor
Michael Hull
Reginald Vear Scowen
Dennis Giles
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Unilever PLC
Unilever NV
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Unilever PLC
Unilever NV
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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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/60Sulfonium or phosphonium 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
    • C11D1/28Sulfonation products derived from fatty acids or their derivatives, e.g. esters, amides
    • 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
    • C11D1/66Non-ionic compounds
    • C11D1/72Ethers of polyoxyalkylene glycols

Definitions

  • This invention relates to a detergent composition, in particular to a detergent composition for washing fabrics.
  • Fabric washing compositions contain, as an essential ingredient, a surfactant system whose role is to assist in the removal of soil from the fabric and its suspension in the wash liquor.
  • Suitable detergent active surfactant materials fall into a number of classes, including anionic, nonionic and cationic materials. Marketed products contain materials selected from one or more of these classes.
  • anionic surfactant materials are the alkyl benzene sulphonates and these provide satisfactory results especially at high temperatures. There has been a desire to find alternative anionic surfactants for use in circumstances when alkyl benzene sulphonates are undesirable.
  • fatty acid ester sulphonates of the general formula where R1 is an alkyl group derived from a fatty acid, usually from a natural source, R2 is a short chain alkyl group, usually methyl and M is, for example, an alkali metal.
  • R1 is an alkyl group derived from a fatty acid, usually from a natural source
  • R2 is a short chain alkyl group, usually methyl
  • M is, for example, an alkali metal.
  • United States patent 4416809 Magneticari et al, assigned to Lion Corporation
  • Exemplified FAES materials are those in which R1 is derived from tallow and R2 is methyl. Ethyl or propyl are also mentioned as possibilities for R2.
  • EP-A-207642 discloses surfactant formulations which are mixtures of anionic surfactant which is either fatty acyl ester sulphonate or an acyl isethionate and a nonionic surfactant.
  • anionic surfactant which is either fatty acyl ester sulphonate or an acyl isethionate
  • nonionic surfactant are stated to be various ethoxylated compounds containing from 2 to 25 ethylene oxide residues.
  • EP-A-231891 discloses concentrates of fatty acyl ester sulphonates containing 50 to 70 wt% of surfactant which surfactant is a mixture of fatty alkyl ester sulphonate and ethoxylated fatty alcohol.
  • the fatty acyl ester sulphonate is preferably a methyl or ethyl ester but esters of alcohols containing from 1 to 4 carbon atoms and esters of longer alcohols up to octanol are also mentioned.
  • the ethoxylated fatty alcohols may be ethoxylated with an average of 3 to 15 ethylene oxide residues and a preference is stated for an average of 3 to 10 ethylene oxide residues.
  • a detergent composition including a surfactant system at least 50% by weight of which comprises:
  • the fatty acid ester sulphonate salts of the above general formula can be produced from fatty acids in conventional manner. Desirable starting fatty acids are, for example, those derived from tallow, palm oil or coconut oil. Thus, it is preferred that the group R1 contains from 12 to 18 carbon atoms. It may be fully or substantially saturated.
  • the group R2 may have fewer carbon atoms than the group R1. For instance the group R2 may have from 4 to 8 carbon atoms. In particular it may be butyl.
  • the sum of the carbon atoms in groups R1 and R2 will preferably lie in the range 12 to 24. It is preferable also that R1 and R2 are different, especially when the sum of the carbon atoms in groups R1 and R2 is 14 or more.
  • a preferred FAES material is that in which R1 is coconut alkyl and R2 is butyl.
  • FAES materials as defined above could be used.
  • Other FAES materials such as the tallow methyl material, may also be included in minor amounts, but there is no particular advantage in doing so.
  • water-soluble salts of these anionic surfactants specifically the alkali metal (sodium or potassium) salts thereof.
  • Suitable nonionic surfactants which may be used are the reaction products of compounds having a hydrophobic group and a reactive hydrogen atom, for example aliphatic alcohols, acids, amides or alkyl phenols with alkylene oxides, especially ethylene oxide either alone or with propylene oxide.
  • Specific nonionic detergent compounds are alkyl (C6 - C22) phenols-ethylene oxide condensates, the condensation products of aliphatic (C8 - C18) primary or secondary linear or branched alcohols with ethylene oxide, and products made by condensation of ethylene oxide with the reaction products of propylene oxide and ethylenediamine.
  • alkylene oxide adducts of fatty materials are used as the nonionic surfactants
  • the number of alkylene oxide groups per molecule has a considerable effect upon the HLB of the nonionic surfactant.
  • the chain length and nature of the fatty material is also influential, and thus the preferred number of alkylene oxide groups per molecule depends upon the nature and chain length of the fatty material.
  • the weight ratio between the anionic surfactant and the alkoxylated nonionic surfactant lies between 4:1 and 1:4, most preferably between 3:1 and 1:2, otherwise the benefits of the invention may not be achieved.
  • compositions according to the invention include the surfactant system in an amount from 2% to 50%, such as from 4% to 30% by weight of the composition.
  • the surfactant system may include other surfactant materials in addition to the specified sulphonate and nonionic materials. These other surfactant materials may be selected from other anionic detergent active materials, zwitterionic or amphoteric detergent active materials or mixtures thereof.
  • any such further surfactant materials will be present at a level which is no more than 50%, preferably no more than 40% of the total amount of surfactant in the composition, and might be not over 5% of the whole composition.
  • the other anionic detergent active materials may be the usual water-soluble alkali metal salts of organic sulphates and sulphonates having alkyl radicals containing from 8 to 22 carbon atoms, the term alkyl being used to include the alkyl portion of higher acyl radicals.
  • suitable synthetic anionic detergent compounds are sodium and potassium alkyl sulphates, especially those obtained by sulphating higher (C8 - C18) alcohols produced for example from tallow or coconut oil, sodium and potassium alkyl (C9 - C20) benzene sulphonates, particularly sodium linear secondary alkyl (C10 - C15) benzene sulphonates; sodium alkyl glyceryl ether sulphates, especially those ethers of the higher alcohols derived from tallow or coconut oil and synthetic alcohols derived from petroleum; sodium coconut oil fatty monoglyceride sulphates and sulphonates; sodium and potassium salts of sulphuric acid esters of higher (C8 - C18) fatty alcohol-alkylene oxide, particularly ethylene oxide, reaction products; the reaction products of fatty acids such as coconut fatty acids esterified with isethionic acid and neutralised with sodium hydroxide; sodium and potassium salts of fatty acid amides of methyl taurine; al
  • compositions of the invention may contain a detergency builder material, this may be any material capable of reducing the level of free calcium ions in the wash liquor and will preferably provide the compositions with other beneficial properties such as the generation of an alkaline pH and the suspension of soil removed from the fabric.
  • Examples of phosphorus-containing inorganic detergency builders when present, include the water-soluble salts, especially alkali metal pyrophosphates, orthophosphates, orthophosphates, polyphosphates and phosphonates.
  • Specific examples of inorganic phosphate builders include sodium and potassium tripolyphosphates, orthophosphates and hexametaphosphates.
  • non-phosphorus-containing inorganic detergency builders when present, include water-soluble alkali metal carbonates, bicarbonates, silicates and crystalline and amorphous aluminosilicates. Specific examples include sodium carbonate (with or without calcite seeds), potassium carbonate (with or without calcite seeds), sodium and potassium bicarbonates and silicates.
  • organic detergency builders when present, include the alkali metal, ammonium and substituted ammonium polyacetates, carboxylates, polycarboxylates, polyacetyl carboxylates and polyhydroxysulphonates. Specific examples include sodium, potassium, lithium, ammonium and substituted ammonium salts of ethylenediaminetetraacetic acid, nitrilotriacetic acid, oxydisuccinic acid, melitic acid, benzene polycarboxylic acids and citric acid.
  • compositions according to the invention be alkaline, that is at the concentration of 1 g/l in distilled water at 25°C the pH should be at least 8, preferably at least 10.
  • the compositions may include a water-soluble alkaline salt. This salt may be a detergency builder or a non-building alkaline material.
  • ingredients which may be present in the composition include fabric softening agents such as fatty amines, fabric softening clay materials, lather boosters such as alkanolamides, particularly the monoethanolamides derived from palm kernel fatty acids and coconut fatty acids, lather depressants, oxygen-releasing bleaching agents such as sodium perborate and sodium percarbonate, peracid bleach precursors, chlorine-releasing bleaching agents such as tricloroisocyanuric acid, inorganic salts such as sodium sulphate, and, usually present in very minor amounts, fluorescent agents, perfumes including deodorant perfumes, enzymes such as proteases, cellulases, amylases and lipase, germicides and colourants.
  • fabric softening agents such as fatty amines, fabric softening clay materials
  • lather boosters such as alkanolamides, particularly the monoethanolamides derived from palm kernel fatty acids and coconut fatty acids
  • lather depressants oxygen-releasing bleaching agents such as sodium perborate
  • the detergent compositions according to the invention may be prepared by a number of different methods according to their physical form.
  • they may be prepared by dry-mixing or coagglomeration.
  • a preferred physical form is a granule incorporating a detergency builder salt and this is most conveniently manufactured by spray-drying at least part of the composition.
  • a slurry is prepared containing the heat-insensitive components of the composition such as the surfactant system, builder material and filler salt.
  • the slurry is spray-dried to form base powder granules with which any solid heat-sensitive ingredients may be mixed, such ingredients including bleaches and enzymes.
  • the specified nonionic surfactants can be liquidified by melting or solvent dissolution and sprayed onto the base powder granules, rather than including them in the slurry for spray-drying.
  • wash liquors were prepared in water having a hardness of 25° FH (equivalent to a free calcium ion concentration of 2.5 x 10 ⁇ 3 molar).
  • the wash liquor contained the equivalent of 6 g/l of a composition containing (by weight) Specified anionic surfactant 9% Specified nonionic surfactant 4% Sodium tripolyphosphate 23% Sodium carbonate 6% Sodium alkaline silicate 5.5% Sodium sulphate 30.8% Sodium chloride 2.93% Water balance
  • the sodium chloride was included as being equivalent in ionic strength to 5% sodium perborate monohydrate which would be present in practice.
  • the bleach is left out of these experiments in order to avoid confusion between detergency and bleaching effect in the interpretation of the results.
  • the wash liquors were used to wash a fabric load at a liquor to cloth ratio of 50:1.
  • the load included a number of polyester monitors to which had previously been applied an amount of C14 tagged triolein. Measurement of the level of tagged triolein after washing, using standard radio-tracer techniques, gives an indication of the degree of detergency, ie. soil removal, obtained.
  • wash time was 20 minutes with an agitation of 70 rpm. Washes were isothermal at 40°C.
  • nonionic surfactant was either SYNPERONIC A7 (ex ICI) which is principally a C13/C15 alcohol ethoxylated with an average of 7 moles ethylene oxide per molecule having an HLB of 11.7, or a 1:3 by weight mixture thereof with SYNPERONIC A3, which is a similar material containing an average of 3 moles of ethylene oxide per molecule, the mixture having an HLB of 9.0.
  • SYNPERONIC A7 ex ICI
  • SYNPERONIC A3 which is a similar material containing an average of 3 moles of ethylene oxide per molecule, the mixture having an HLB of 9.0.
  • CM Coconut methyl FAES TEXIN ES 68: A tallow methyl FAES ex Henkel LB: C12 alkyl butyl FAES
  • CM coconut methyl FAES TEXIN ES 68: A tallow methyl FAES ex Henkel LB: C12 alkyl butyl FAES
  • CM Example No Anionic Nonionic % soil removal 1 CM A7 20.1 2 ES68 A7 20.6 3 LB A7 19.8 4 CM A7/A3 26.0 5 ES68 A7/A3 23.9 6 LB A7/A3 36.2

Description

  • This invention relates to a detergent composition, in particular to a detergent composition for washing fabrics.
  • Fabric washing compositions contain, as an essential ingredient, a surfactant system whose role is to assist in the removal of soil from the fabric and its suspension in the wash liquor. Suitable detergent active surfactant materials fall into a number of classes, including anionic, nonionic and cationic materials. Marketed products contain materials selected from one or more of these classes.
  • The most widely used anionic surfactant materials are the alkyl benzene sulphonates and these provide satisfactory results especially at high temperatures. There has been a desire to find alternative anionic surfactants for use in circumstances when alkyl benzene sulphonates are undesirable.
  • Among such alternative anionic surfactants are the fatty acid ester sulphonates (FAES) of the general formula
    Figure imgb0001

    where R¹ is an alkyl group derived from a fatty acid, usually from a natural source, R² is a short chain alkyl group, usually methyl and M is, for example, an alkali metal. Thus for example, United States patent 4416809 (Magari et al, assigned to Lion Corporation) discloses a composition containing FAES, soap and the salt of a polycarboxylic acid. Exemplified FAES materials are those in which R¹ is derived from tallow and R² is methyl. Ethyl or propyl are also mentioned as possibilities for R².
  • EP-A-207642 discloses surfactant formulations which are mixtures of anionic surfactant which is either fatty acyl ester sulphonate or an acyl isethionate and a nonionic surfactant. The defined fatty acyl ester sulphonates are defined such that the residue of an esterifying alcohol contains from 1 to 5 carbon atoms. The nonionic surfactants are stated to be various ethoxylated compounds containing from 2 to 25 ethylene oxide residues.
  • EP-A-231891 discloses concentrates of fatty acyl ester sulphonates containing 50 to 70 wt% of surfactant which surfactant is a mixture of fatty alkyl ester sulphonate and ethoxylated fatty alcohol. The fatty acyl ester sulphonate is preferably a methyl or ethyl ester but esters of alcohols containing from 1 to 4 carbon atoms and esters of longer alcohols up to octanol are also mentioned. The ethoxylated fatty alcohols may be ethoxylated with an average of 3 to 15 ethylene oxide residues and a preference is stated for an average of 3 to 10 ethylene oxide residues.
  • We have found, however, that the performance of FAES materials in which R² is short chain alkyl is unsatisfactory when the compositions also contain low HLB nonionic surfactants. Since the use of such nonionic surfactants has been shown to lead to a number of benefits, including an overall boosting in detergency (see GB 1241754 - Unilever), there is a desire to improve the performance of FAES materials in the presence of such nonionic materials.
  • We have now surprisingly discovered that this object can be achieved by the use of materials in which R² is butyl or higher alkyl.
  • Thus, according to the invention, there is provided a detergent composition including a surfactant system at least 50% by weight of which comprises:
    • i) a fatty acid ester sulphonate; and
    • ii) a nonionic surfactant having an HLB of less than 10.5, preferably less than 9.5;
      wherein the fatty acid ester sulphonate has the general formula
      Figure imgb0002
      where R¹ and R² are independently hydrocarbon groups having at least 4 carbon atoms, the sum of the carbon atoms in groups R¹ and R² being from 8 to 30, and M is a monovalent cationic species.
  • The fatty acid ester sulphonate salts of the above general formula can be produced from fatty acids in conventional manner. Desirable starting fatty acids are, for example, those derived from tallow, palm oil or coconut oil. Thus, it is preferred that the group R¹ contains from 12 to 18 carbon atoms. It may be fully or substantially saturated. The group R² may have fewer carbon atoms than the group R¹. For instance the group R² may have from 4 to 8 carbon atoms. In particular it may be butyl.
  • The sum of the carbon atoms in groups R¹ and R² will preferably lie in the range 12 to 24. It is preferable also that R¹ and R² are different, especially when the sum of the carbon atoms in groups R¹ and R² is 14 or more. A preferred FAES material is that in which R¹ is coconut alkyl and R² is butyl.
  • Mixtures of FAES materials as defined above could be used. Other FAES materials, such as the tallow methyl material, may also be included in minor amounts, but there is no particular advantage in doing so.
  • It is preferred to use the water-soluble salts of these anionic surfactants, specifically the alkali metal (sodium or potassium) salts thereof.
  • Suitable nonionic surfactants which may be used are the reaction products of compounds having a hydrophobic group and a reactive hydrogen atom, for example aliphatic alcohols, acids, amides or alkyl phenols with alkylene oxides, especially ethylene oxide either alone or with propylene oxide. Specific nonionic detergent compounds are alkyl (C₆ - C₂₂) phenols-ethylene oxide condensates, the condensation products of aliphatic (C₈ - C₁₈) primary or secondary linear or branched alcohols with ethylene oxide, and products made by condensation of ethylene oxide with the reaction products of propylene oxide and ethylenediamine.
  • When alkylene oxide adducts of fatty materials are used as the nonionic surfactants, the number of alkylene oxide groups per molecule has a considerable effect upon the HLB of the nonionic surfactant. The chain length and nature of the fatty material is also influential, and thus the preferred number of alkylene oxide groups per molecule depends upon the nature and chain length of the fatty material.
  • We have found it of advantage that the weight ratio between the anionic surfactant and the alkoxylated nonionic surfactant lies between 4:1 and 1:4, most preferably between 3:1 and 1:2, otherwise the benefits of the invention may not be achieved.
  • Preferred compositions according to the invention include the surfactant system in an amount from 2% to 50%, such as from 4% to 30% by weight of the composition.
  • The surfactant system may include other surfactant materials in addition to the specified sulphonate and nonionic materials. These other surfactant materials may be selected from other anionic detergent active materials, zwitterionic or amphoteric detergent active materials or mixtures thereof.
  • Any such further surfactant materials will be present at a level which is no more than 50%, preferably no more than 40% of the total amount of surfactant in the composition, and might be not over 5% of the whole composition.
  • The other anionic detergent active materials may be the usual water-soluble alkali metal salts of organic sulphates and sulphonates having alkyl radicals containing from 8 to 22 carbon atoms, the term alkyl being used to include the alkyl portion of higher acyl radicals. Examples of suitable synthetic anionic detergent compounds are sodium and potassium alkyl sulphates, especially those obtained by sulphating higher (C₈ - C₁₈) alcohols produced for example from tallow or coconut oil, sodium and potassium alkyl (C₉ - C₂₀) benzene sulphonates, particularly sodium linear secondary alkyl (C₁₀ - C₁₅) benzene sulphonates; sodium alkyl glyceryl ether sulphates, especially those ethers of the higher alcohols derived from tallow or coconut oil and synthetic alcohols derived from petroleum; sodium coconut oil fatty monoglyceride sulphates and sulphonates; sodium and potassium salts of sulphuric acid esters of higher (C₈ - C₁₈) fatty alcohol-alkylene oxide, particularly ethylene oxide, reaction products; the reaction products of fatty acids such as coconut fatty acids esterified with isethionic acid and neutralised with sodium hydroxide; sodium and potassium salts of fatty acid amides of methyl taurine; alkane monosulphonates such as those derived by reacting alpha-olefins (C₈ - C₂₀) with sodium bisulphite and those derived from reacting paraffins with SO₂ and C1₂ and then hydrolysing with a base to product a random sulphate.
  • The compositions of the invention may contain a detergency builder material, this may be any material capable of reducing the level of free calcium ions in the wash liquor and will preferably provide the compositions with other beneficial properties such as the generation of an alkaline pH and the suspension of soil removed from the fabric.
  • Examples of phosphorus-containing inorganic detergency builders, when present, include the water-soluble salts, especially alkali metal pyrophosphates, orthophosphates, orthophosphates, polyphosphates and phosphonates. Specific examples of inorganic phosphate builders include sodium and potassium tripolyphosphates, orthophosphates and hexametaphosphates.
  • Examples of non-phosphorus-containing inorganic detergency builders, when present, include water-soluble alkali metal carbonates, bicarbonates, silicates and crystalline and amorphous aluminosilicates. Specific examples include sodium carbonate (with or without calcite seeds), potassium carbonate (with or without calcite seeds), sodium and potassium bicarbonates and silicates.
  • Examples of organic detergency builders, when present, include the alkali metal, ammonium and substituted ammonium polyacetates, carboxylates, polycarboxylates, polyacetyl carboxylates and polyhydroxysulphonates. Specific examples include sodium, potassium, lithium, ammonium and substituted ammonium salts of ethylenediaminetetraacetic acid, nitrilotriacetic acid, oxydisuccinic acid, melitic acid, benzene polycarboxylic acids and citric acid.
  • It is preferred that the compositions according to the invention be alkaline, that is at the concentration of 1 g/l in distilled water at 25°C the pH should be at least 8, preferably at least 10. To this end the compositions may include a water-soluble alkaline salt. This salt may be a detergency builder or a non-building alkaline material.
  • Apart from the ingredients already mentioned, a number of optional ingredients may also be present.
  • Examples of other ingredients which may be present in the composition include fabric softening agents such as fatty amines, fabric softening clay materials, lather boosters such as alkanolamides, particularly the monoethanolamides derived from palm kernel fatty acids and coconut fatty acids, lather depressants, oxygen-releasing bleaching agents such as sodium perborate and sodium percarbonate, peracid bleach precursors, chlorine-releasing bleaching agents such as tricloroisocyanuric acid, inorganic salts such as sodium sulphate, and, usually present in very minor amounts, fluorescent agents, perfumes including deodorant perfumes, enzymes such as proteases, cellulases, amylases and lipase, germicides and colourants.
  • The detergent compositions according to the invention may be prepared by a number of different methods according to their physical form. In the case of granular products they may be prepared by dry-mixing or coagglomeration. A preferred physical form is a granule incorporating a detergency builder salt and this is most conveniently manufactured by spray-drying at least part of the composition. In this process a slurry is prepared containing the heat-insensitive components of the composition such as the surfactant system, builder material and filler salt. The slurry is spray-dried to form base powder granules with which any solid heat-sensitive ingredients may be mixed, such ingredients including bleaches and enzymes. The specified nonionic surfactants can be liquidified by melting or solvent dissolution and sprayed onto the base powder granules, rather than including them in the slurry for spray-drying. The invention will now be described in more detail in the following non-limiting examples.
  • EXAMPLES 1 TO 6
  • Wash liquors were prepared in water having a hardness of 25° FH (equivalent to a free calcium ion concentration of 2.5 x 10⁻³ molar). The wash liquor contained the equivalent of 6 g/l of a composition containing (by weight)
    Specified anionic surfactant 9%
    Specified nonionic surfactant 4%
    Sodium tripolyphosphate 23%
    Sodium carbonate 6%
    Sodium alkaline silicate 5.5%
    Sodium sulphate 30.8%
    Sodium chloride 2.93%
    Water balance
  • The sodium chloride was included as being equivalent in ionic strength to 5% sodium perborate monohydrate which would be present in practice. The bleach is left out of these experiments in order to avoid confusion between detergency and bleaching effect in the interpretation of the results.
  • The wash liquors were used to wash a fabric load at a liquor to cloth ratio of 50:1. The load included a number of polyester monitors to which had previously been applied an amount of C¹⁴ tagged triolein. Measurement of the level of tagged triolein after washing, using standard radio-tracer techniques, gives an indication of the degree of detergency, ie. soil removal, obtained.
  • The wash time was 20 minutes with an agitation of 70 rpm. Washes were isothermal at 40°C.
  • In each case the nonionic surfactant was either SYNPERONIC A7 (ex ICI) which is principally a C₁₃/C₁₅ alcohol ethoxylated with an average of 7 moles ethylene oxide per molecule having an HLB of 11.7, or a 1:3 by weight mixture thereof with SYNPERONIC A3, which is a similar material containing an average of 3 moles of ethylene oxide per molecule, the mixture having an HLB of 9.0. "Synperonic" is a Registered Trade Mark.
  • The anionic surfactants used were:
    CM: Coconut methyl FAES
    TEXIN ES 68: A tallow methyl FAES ex Henkel
    LB: C₁₂ alkyl butyl FAES
    The results obtained were as follows:
    Example No Anionic Nonionic % soil removal
    1 CM A7 20.1
    2 ES68 A7 20.6
    3 LB A7 19.8
    4 CM A7/A3 26.0
    5 ES68 A7/A3 23.9
    6 LB A7/A3 36.2

    These results show that in the presence of the higher HLB nonionic material (Examples 1 to 3) there is very little difference between the anionic surfactants tested. In the presence of the lower HLB nonionic mixture (A7/A3) however, significant preference for the C₁₂ butyl FAES over the others tested is evident.

Claims (6)

  1. A detergent composition including a surfactant system, characterized in that such surfactant system comprises at least 50% by weight of:
    i) a fatty acid ester sulphonate; and
    ii) a nonionic surfactant having an HLB of less than 10.5;
    wherein the fatty acid ester sulphonate has the general formula
    Figure imgb0003
    wherein R¹ and R² are independently hydrocarbon groups having at least 4 carbon atoms, the sum of the carbon atoms in groups R¹ and R² being from 8 to 30, and M is a monovalent cationic species.
  2. A detergent composition according to claim 1 wherein the sum of the carbon atoms in groups R¹ and R² is from 12 to 24 carbon atoms.
  3. A detergent composition according to claim 1 or claim 2 wherein the group R¹ is a hydrocarbon group containing from 12 to 18 carbon atoms.
  4. A detergent composition according to claim 1, wherein the fatty acid ester sulphonate is an alkali metal salt of the sulphonate of the butyl ester of coconut fatty acid.
  5. A detergent composition according to any one of the preceding claims wherein the nonionic surfactant has an HLB of 9.5 or less.
  6. A detergent composition according to any one of the preceding claims wherein the surfactant system constitutes from 2 to 50% by weight of the whole composition.
EP89303376A 1988-04-06 1989-04-05 Detergent composition Expired - Lifetime EP0336740B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB888808041A GB8808041D0 (en) 1988-04-06 1988-04-06 Detergent composition
GB8808041 1988-04-06

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EP0336740A2 EP0336740A2 (en) 1989-10-11
EP0336740A3 EP0336740A3 (en) 1990-03-28
EP0336740B1 true EP0336740B1 (en) 1995-01-25

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EP (1) EP0336740B1 (en)
JP (1) JPH06102794B2 (en)
KR (1) KR960000199B1 (en)
AU (1) AU619266B2 (en)
BR (1) BR8901573A (en)
CA (1) CA1323818C (en)
DE (1) DE68920768T2 (en)
ES (1) ES2068240T3 (en)
GB (1) GB8808041D0 (en)
IN (1) IN167967B (en)
MY (1) MY104422A (en)
OA (1) OA09035A (en)
PH (1) PH27191A (en)
TR (1) TR24063A (en)
ZA (1) ZA892470B (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001092457A1 (en) * 2000-06-01 2001-12-06 Huish Detergents, Inc. COMPOSITIONS CONTAINING α-SULFOFATTY ACID ESTERS AND METHODS OF MAKING THE SAME
US6770611B2 (en) 2000-01-11 2004-08-03 Huish Detergents, Inc. α-sulfofatty acid ester laundry detergent composition with reduced builder deposits
US7459420B2 (en) 2004-12-01 2008-12-02 Vlahakis E Van Automatic dishwashing detergent comprised of ethylene oxide adduct and without phosphates
US7485613B2 (en) 2004-12-01 2009-02-03 Venus Laboratories, Inc. Low foaming carpet-cleaning detergent concentrate comprised of ethylene oxide adduct and without phosphates
US7632798B2 (en) 2000-05-24 2009-12-15 The Sun Products Corporation Composition containing α-sulfofatty acid ester and hydrotrope and methods of making and using the same
US7772176B2 (en) 2000-05-19 2010-08-10 The Sun Products Corporation Detergent compositions containing α-sulfofatty acid esters and methods of making and using the same

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EP0792336A2 (en) * 1995-09-18 1997-09-03 Stepan Company Heavy duty liquid detergent compositions comprising salts of alpha sulfonated fatty acid methyl esters and use of alpha-sulphonated fatty acid salts to inhibit redeposition of soil on fabric
US5945394A (en) * 1995-09-18 1999-08-31 Stepan Company Heavy duty liquid detergent compositions comprising salts of α-sulfonated fatty acid methyl esters and use of α-sulphonated fatty acid salts to inhibit redeposition of soil on fabric
US6780830B1 (en) * 2000-05-19 2004-08-24 Huish Detergents, Incorporated Post-added α-sulfofatty acid ester compositions and methods of making and using the same
US6534464B1 (en) 2000-05-19 2003-03-18 Huish Detergents, Inc. Compositions containing α-sulfofatty acid ester and polyalkoxylated alkanolamide and methods of making and using the same
US6764989B1 (en) 2000-10-02 2004-07-20 Huish Detergents, Inc. Liquid cleaning composition containing α-sulfofatty acid ester
WO2016160407A1 (en) * 2015-03-31 2016-10-06 Stepan Company Detergents based on alpha-sulfonated fatty ester surfactants

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JPS4964609A (en) * 1972-10-25 1974-06-22
CA1033638A (en) * 1974-09-11 1978-06-27 The Procter And Gamble Company Detergent compositions
JPS54132609A (en) * 1978-04-07 1979-10-15 Nippon Oil & Fats Co Ltd Detergent for raw wool
JPS55108496A (en) * 1979-02-13 1980-08-20 Nippon Gousei Senzai Kk Detergent composition
JPS57180699A (en) * 1981-04-30 1982-11-06 Lion Corp Granular detergent composition
GB8515762D0 (en) * 1985-06-21 1985-07-24 Ici Plc Surfactant composition
DE3603580A1 (en) * 1986-02-06 1987-08-13 Henkel Kgaa ESTERSULPHONATE CONTAINING TENSIDE CONCENTRATES AND THEIR USE

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6770611B2 (en) 2000-01-11 2004-08-03 Huish Detergents, Inc. α-sulfofatty acid ester laundry detergent composition with reduced builder deposits
US7772176B2 (en) 2000-05-19 2010-08-10 The Sun Products Corporation Detergent compositions containing α-sulfofatty acid esters and methods of making and using the same
US8030264B2 (en) 2000-05-19 2011-10-04 The Sun Products Corporation Detergent containing α-sulfofatty acid esters and methods of making and using the same
US7632798B2 (en) 2000-05-24 2009-12-15 The Sun Products Corporation Composition containing α-sulfofatty acid ester and hydrotrope and methods of making and using the same
US8017570B2 (en) 2000-05-24 2011-09-13 The Sun Products Corporation Composition containing α-sulfofatty acid ester and hydrotrope and methods of making and using the same
WO2001092457A1 (en) * 2000-06-01 2001-12-06 Huish Detergents, Inc. COMPOSITIONS CONTAINING α-SULFOFATTY ACID ESTERS AND METHODS OF MAKING THE SAME
US7459420B2 (en) 2004-12-01 2008-12-02 Vlahakis E Van Automatic dishwashing detergent comprised of ethylene oxide adduct and without phosphates
US7485613B2 (en) 2004-12-01 2009-02-03 Venus Laboratories, Inc. Low foaming carpet-cleaning detergent concentrate comprised of ethylene oxide adduct and without phosphates

Also Published As

Publication number Publication date
GB8808041D0 (en) 1988-05-05
KR890016151A (en) 1989-11-28
MY104422A (en) 1994-03-30
EP0336740A2 (en) 1989-10-11
ES2068240T3 (en) 1995-04-16
JPH06102794B2 (en) 1994-12-14
AU619266B2 (en) 1992-01-23
EP0336740A3 (en) 1990-03-28
JPH01299897A (en) 1989-12-04
DE68920768D1 (en) 1995-03-09
IN167967B (en) 1991-01-12
BR8901573A (en) 1989-11-21
AU3239889A (en) 1989-10-12
CA1323818C (en) 1993-11-02
PH27191A (en) 1993-04-16
KR960000199B1 (en) 1996-01-03
OA09035A (en) 1991-03-31
ZA892470B (en) 1990-12-28
DE68920768T2 (en) 1995-07-13
TR24063A (en) 1991-02-22

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