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EP0506312B1 - Use of fabric softening composition - Google Patents

Use of fabric softening composition Download PDF

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Publication number
EP0506312B1
EP0506312B1 EP92302453A EP92302453A EP0506312B1 EP 0506312 B1 EP0506312 B1 EP 0506312B1 EP 92302453 A EP92302453 A EP 92302453A EP 92302453 A EP92302453 A EP 92302453A EP 0506312 B1 EP0506312 B1 EP 0506312B1
Authority
EP
European Patent Office
Prior art keywords
quaternary ammonium
weight
ammonium material
fabric softening
compositions
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.)
Expired - Lifetime
Application number
EP92302453A
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German (de)
French (fr)
Other versions
EP0506312A1 (en
Inventor
Simon Richard Unilever Research Ellis
Graham Andrew Unilever Research Turner
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
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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
    • C11D1/66Non-ionic compounds
    • C11D1/835Mixtures of non-ionic with cationic 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
    • C11D3/001Softening 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
    • C11D1/38Cationic compounds
    • C11D1/62Quaternary ammonium 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 the use as a soil release agent in a fabric softening composition of a biodegradable quaternary ammonium material.
  • Rinse added fabric softener compositions are well known. Typically such compositions contain a water insoluble quaternary ammonium fabric softening agent dispersed in water at a level of softening agent up to 7% by weight in which case the compositions are considered dilute, or at levels from 7% to 50% in which case the compositions are considered concentrates.
  • fabric softening compositions desirably have other benefits. One is the ability to confer soil release properties to fabrics, particularly those woven from polyester fibres.
  • viscosity control agents In the past physical stability of rinse added fabric softener compositions has been improved by the addition of viscosity control agents or anti-gelling agents.
  • viscosity control agents For example in EP 13780 (Procter and Gamble) viscosity control agents are added to certain concentrated compositions. The agents may include C10-C18 fatty alcohols.
  • EP 280550 More recently in EP 280550 (Unilever) it has been proposed to improve the physical stability of dilute compositions comprising biodegradable, ester-linked quaternary ammonium compounds and fatty acid by the addition of nonionic surfactants.
  • compositions comprising biodegradable ester-linked quaternary ammonium compounds the problem of physical instability is more acute than with traditional quaternary ammonium compounds.
  • a nonionic emulsifier/stabiliser is added to a concentrate comprising an ester-linked quaternary ammonium compound to form a viscous gel.
  • the stabiliser is a C12 to C14 alcohol ethoxylated with 9 molecules of ethylene oxide. The degree of branching of the alcohol is not however mentioned.
  • Certain nonionic stabilising agents not only stabilise concentrated compositions comprising biodegradable quaternary ammonium compounds but are also environmentally friendly, in that they show acceptable biodegradability and are not substantially toxic in aquatic systems.
  • Soil release properties are generally imparted to fabrics by the use of separate soil-release agents, usually a high molecular weight polymer, in a detergent composition or separate treatment.
  • separate soil-release agents usually a high molecular weight polymer
  • a cationic polymeric soil release agent for use in a fabric conditioning composition.
  • a disadvantage of such compositions is that the soil release agent increases the number of components in the formulation, increasing cost and making the product less environmentally acceptable.
  • EP-A-0,234,311 describes the use of insoluble polyfunctional quaternary ammonium compounds as soil collectors, to regenerate soil-laden detergent solutions.
  • the document contains no specific mention of the quaternary ammonium materials to which the present invention relates.
  • EP-A-0,309,052 describes the use of quaternary ammonium salts containing at least one ester linkage as softeners in shelf-stable and biodegradable fabric softening compositions.
  • the compositions also include a linear alkoxylated alcohol.
  • fabric softening compositions comprising biodegradable ester-linked quaternary ammonium compounds may confer soil release properties to fabrics without the use of a separate soil release agent.
  • a soil release agent in a fabric softening composition of a quaternary ammonium material comprising a compound having two C12 ⁇ 28 alkyl or alkenyl groups connected via an ester link to the quaternary nitrogen atom.
  • composition is a liquid comprising an aqueous base.
  • a preferred type of ester-linked quaternary ammonium material for use in the compositions according to the invention can be represented by the formula: wherein R1 is an alkyl or hydroxyalkyl group containing from 1 to 4 carbon atoms; and R2 is a C11-C23 alkyl chain.
  • Preferred materials of this class and their method of preparation are, for example, described in US 4 137 180 (Lever Brothers).
  • these materials comprise small amounts of the corresponding monoester as described in US 4 137 180 for example 1-tallowoxy, 2-hydroxytrimethyl ammonium propane chloride.
  • the level of ester linked quaternary ammonium compounds is at least 1% by weight of the composition, more preferably more than 3% by weight of the composition; especially interesting are concentrated compositions which comprise more than 7% of ester-linked quaternary ammonium compound.
  • the level of ester-linked quaternary ammonium compounds preferably is between 1% and 80% by weight, more preferably 3% to 50%, most preferably 8% to 50%.
  • the softening composition may be stabilised at low temperatures by the addition of nonionic stabilisers.
  • Suitable nonionic stabilisers which can be used include the condensation products of C8 - C22 primary linear alcohols with 10 to 20 moles of ethylene oxide. The alcohols may be saturated or unsaturated.
  • the nonionic stabiliser has an HLB of between 10 and 20, more preferably 12 and 20.
  • the nonionic stabiliser is biodegradable and has low aquatic toxicity.
  • Use of less than 10 moles of ethylene oxide results in an acceptable acute aquatic toxicity value of > 1 mg/l EC50 48 hours for daphnia and algae and EC50 96 hours for fish, especially if the HLB of the nonionic is less than 12.
  • the level of nonionic stabiliser is within the range from 0.1 to 10% by weight, more preferably from 0.5 to 5% by weight, most preferably from 1 to 4% by weight.
  • the mole ratio of the quaternary ammonium compound to the nonionic stabilising agent is within the range from 40:1 to about 1:1, preferably within the range from 18:1 to about 3:1.
  • the composition can also contain fatty acids for example C8 - C24 alkyl or alkenyl monocarboxylic acids or polymers thereof.
  • fatty acids for example C8 - C24 alkyl or alkenyl monocarboxylic acids or polymers thereof.
  • saturated fatty acids are used, in particular, hardened tallow C16-C18 fatty acids.
  • the fatty acid is non-saponified, more preferably the fatty acid is free for example oleic acid, lauric acid or tallow fatty acid.
  • the level of fatty acid material is preferably more than 0.1% by weight, more preferably more than 0.2% by weight. Especially preferred are concentrates comprising from 0.5 to 20% by weight of fatty acid, more preferably 1% to 10% by weight.
  • the weight ratio of quaternary ammonium material to fatty acid material is preferably from 10:1 to 1:10.
  • compositions of the invention preferably have a pH of more than 2.0, more preferably less than 5.
  • the composition can also contain one or more optional ingredients, selected from non-aqueous solvents, pH buffering agents, perfumes, perfume carriers, fluorescers, colourants, hydrotropes, antifoaming agents, antiredeposition agents, enzymes, optical brightening agents, opacifiers, anti-shrinking agents, anti-wrinkle agents, anti-spotting agents, germicides, fungicides, anti-oxidants, anti-corrosion agents, drape imparting agents, antistatic agents and ironing aids.
  • optional ingredients selected from non-aqueous solvents, pH buffering agents, perfumes, perfume carriers, fluorescers, colourants, hydrotropes, antifoaming agents, antiredeposition agents, enzymes, optical brightening agents, opacifiers, anti-shrinking agents, anti-wrinkle agents, anti-spotting agents, germicides, fungicides, anti-oxidants, anti-corrosion agents, drape imparting agents, antistatic agents and ironing aids.
  • composition may also contain nonionic fabric softening agents such as lanolin and derivatives thereof.
  • Liquid fabric softening compositions were made as follows.
  • the cationic fabric softening agent, fatty acid and nonionic stabilising agent where appropriate were premixed and heated together to form a clear melt.
  • the molten mixture thus formed was added over a period of at least one minute, to water at 70°C to 80°C with constant stirring to form a dispersion.
  • the soil release properties imparted to polyester test pieces by treatment with the compositions was assessed by measuring the change in reflectance following staining and a subsequent wash in a proprietary detergent composition.
  • the pieces were first rinsed for 5 minutes in 1 litre of 14°FH water containing 0.67 ml of either composition.
  • the pieces were then line dried and stained with 100 micro litres of olive oil containing 0.06% sudan red dye.
  • the stain was allowed to spread for a minimum of two days following which the reflectance of the stained piece (R1) was measured using an ICS micromatch.
  • the pieces were then washed, rinsed and line dried using 5q/1 New System Persil Automatic (Trade Mark) in 14°FH water for a 15 minute wash cycle.
  • composition B shows a smaller soil release benefit than compositions according to the invention (Composition A).
  • Liquid fabric softening compositions as given below were made as described in Example 1.
  • the soil release properties of the compositions were measured as described in Example 1 excepting that the pieces were first rinsed in 1 litre of 14°FH water containing 2ml of either composition.
  • compositions comprising ester-linked quaternaries show a soil release benefit greater than that obtained from compositions comprising conventional quaternary and that the benefit is seen in the absence of a nonionic stabilising agent.
  • Example 2 was repeated with a composition which did not contain any nonionic to show that the improved soil release benefit is due entirely to the use of the biodegradable ester linked quaternary ammonium compound.

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  • 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)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Detergent Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

  • The present invention relates to the use as a soil release agent in a fabric softening composition of a biodegradable quaternary ammonium material.
  • Rinse added fabric softener compositions are well known. Typically such compositions contain a water insoluble quaternary ammonium fabric softening agent dispersed in water at a level of softening agent up to 7% by weight in which case the compositions are considered dilute, or at levels from 7% to 50% in which case the compositions are considered concentrates. In addition to softening, fabric softening compositions desirably have other benefits. One is the ability to confer soil release properties to fabrics, particularly those woven from polyester fibres.
  • One of the problems associated with fabric softening compositions is the physical instability of such compositions when stored. This problem is accentuated by having a concentrated composition and by storage at low temperatures.
  • Concentrates and storage stability at low temperatures are, however, desired by the consumer. Physical instability manifests itself as a thickening on storage of the composition to a level where the composition is no longer pourable and can even lead to the formation of an irreversible gel. The thickening is very undesirable since the composition can no longer be conveniently used.
  • In the past physical stability of rinse added fabric softener compositions has been improved by the addition of viscosity control agents or anti-gelling agents. For example in EP 13780 (Procter and Gamble) viscosity control agents are added to certain concentrated compositions. The agents may include C₁₀-C₁₈ fatty alcohols. More recently in EP 280550 (Unilever) it has been proposed to improve the physical stability of dilute compositions comprising biodegradable, ester-linked quaternary ammonium compounds and fatty acid by the addition of nonionic surfactants.
  • With concentrated compositions comprising biodegradable ester-linked quaternary ammonium compounds the problem of physical instability is more acute than with traditional quaternary ammonium compounds.
  • In EP 0 040 562 (Lesieur Cotelle) a nonionic emulsifier/stabiliser is added to a concentrate comprising an ester-linked quaternary ammonium compound to form a viscous gel. The stabiliser is a C₁₂ to C₁₄ alcohol ethoxylated with 9 molecules of ethylene oxide. The degree of branching of the alcohol is not however mentioned.
  • Certain nonionic stabilising agents not only stabilise concentrated compositions comprising biodegradable quaternary ammonium compounds but are also environmentally friendly, in that they show acceptable biodegradability and are not substantially toxic in aquatic systems.
  • Soil release properties are generally imparted to fabrics by the use of separate soil-release agents, usually a high molecular weight polymer, in a detergent composition or separate treatment. For example in EP 0 398 133A (Procter & Gamble) there is disclosed a cationic polymeric soil release agent for use in a fabric conditioning composition.
  • A disadvantage of such compositions is that the soil release agent increases the number of components in the formulation, increasing cost and making the product less environmentally acceptable.
  • EP-A-0,234,311 describes the use of insoluble polyfunctional quaternary ammonium compounds as soil collectors, to regenerate soil-laden detergent solutions. The document contains no specific mention of the quaternary ammonium materials to which the present invention relates.
  • EP-A-0,309,052 describes the use of quaternary ammonium salts containing at least one ester linkage as softeners in shelf-stable and biodegradable fabric softening compositions. The compositions also include a linear alkoxylated alcohol.
  • We have now found that fabric softening compositions comprising biodegradable ester-linked quaternary ammonium compounds may confer soil release properties to fabrics without the use of a separate soil release agent.
  • According to the invention there is provided the use as a soil release agent in a fabric softening composition of a quaternary ammonium material comprising a compound having two C₁₂₋₂₈ alkyl or alkenyl groups connected via an ester link to the quaternary nitrogen atom.
  • Preferably the composition is a liquid comprising an aqueous base.
  • A preferred type of ester-linked quaternary ammonium material for use in the compositions according to the invention can be represented by the formula:
    Figure imgb0001
    wherein R₁ is an alkyl or hydroxyalkyl group containing from 1 to 4 carbon atoms; and R₂ is a C₁₁-C₂₃ alkyl chain.
  • Preferred materials of this class and their method of preparation are, for example, described in US 4 137 180 (Lever Brothers). Preferably these materials comprise small amounts of the corresponding monoester as described in US 4 137 180 for example 1-tallowoxy, 2-hydroxytrimethyl ammonium propane chloride.
  • Preferably the level of ester linked quaternary ammonium compounds is at least 1% by weight of the composition, more preferably more than 3% by weight of the composition; especially interesting are concentrated compositions which comprise more than 7% of ester-linked quaternary ammonium compound. The level of ester-linked quaternary ammonium compounds preferably is between 1% and 80% by weight, more preferably 3% to 50%, most preferably 8% to 50%.
  • The softening composition may be stabilised at low temperatures by the addition of nonionic stabilisers. Suitable nonionic stabilisers which can be used include the condensation products of C₈ - C₂₂ primary linear alcohols with 10 to 20 moles of ethylene oxide. The alcohols may be saturated or unsaturated. In particular Genapol T-110, Genapol T-150, Genapol T-200, Genapol C-200 (all Trade Marks; all ex Hoechst AG), Lutensol AT18 (Trade Mark) ex BASF, Genapol 0-100 and Genapol 0-150 (Trade Marks) ex Hoechst, or fatty alcohols for example Laurex CS (Trade Mark), ex Albright and Wilson or Adol 340 (Trade Mark) ex Sherex. Preferably the nonionic stabiliser has an HLB of between 10 and 20, more preferably 12 and 20.
  • Advantageously the nonionic stabiliser is biodegradable and has low aquatic toxicity. Use of less than 10 moles of ethylene oxide results in an acceptable acute aquatic toxicity value of > 1 mg/l EC₅₀ 48 hours for daphnia and algae and EC₅₀ 96 hours for fish, especially if the HLB of the nonionic is less than 12.
  • Preferably, the level of nonionic stabiliser is within the range from 0.1 to 10% by weight, more preferably from 0.5 to 5% by weight, most preferably from 1 to 4% by weight. The mole ratio of the quaternary ammonium compound to the nonionic stabilising agent is within the range from 40:1 to about 1:1, preferably within the range from 18:1 to about 3:1.
  • The composition can also contain fatty acids for example C₈ - C₂₄ alkyl or alkenyl monocarboxylic acids or polymers thereof. Preferably saturated fatty acids are used, in particular, hardened tallow C₁₆-C₁₈ fatty acids. Preferably the fatty acid is non-saponified, more preferably the fatty acid is free for example oleic acid, lauric acid or tallow fatty acid.
  • The level of fatty acid material is preferably more than 0.1% by weight, more preferably more than 0.2% by weight. Especially preferred are concentrates comprising from 0.5 to 20% by weight of fatty acid, more preferably 1% to 10% by weight. The weight ratio of quaternary ammonium material to fatty acid material is preferably from 10:1 to 1:10.
  • The compositions of the invention preferably have a pH of more than 2.0, more preferably less than 5.
  • The composition can also contain one or more optional ingredients, selected from non-aqueous solvents, pH buffering agents, perfumes, perfume carriers, fluorescers, colourants, hydrotropes, antifoaming agents, antiredeposition agents, enzymes, optical brightening agents, opacifiers, anti-shrinking agents, anti-wrinkle agents, anti-spotting agents, germicides, fungicides, anti-oxidants, anti-corrosion agents, drape imparting agents, antistatic agents and ironing aids.
  • The composition may also contain nonionic fabric softening agents such as lanolin and derivatives thereof.
  • The invention will now be illustrated by the following examples. In the examples all percentages are expressed by weight.
  • Example 1
  • Liquid fabric softening compositions were made as follows.
  • The cationic fabric softening agent, fatty acid and nonionic stabilising agent where appropriate were premixed and heated together to form a clear melt. The molten mixture thus formed was added over a period of at least one minute, to water at 70°C to 80°C with constant stirring to form a dispersion.
  • The soil release properties imparted to polyester test pieces by treatment with the compositions was assessed by measuring the change in reflectance following staining and a subsequent wash in a proprietary detergent composition. The pieces were first rinsed for 5 minutes in 1 litre of 14°FH water containing 0.67 ml of either composition. The pieces were then line dried and stained with 100 micro litres of olive oil containing 0.06% sudan red dye. The stain was allowed to spread for a minimum of two days following which the reflectance of the stained piece (R₁) was measured using an ICS micromatch. The pieces were then washed, rinsed and line dried using 5q/1 New System Persil Automatic (Trade Mark) in 14°FH water for a 15 minute wash cycle. The reflectance of the pretreated, washed piece (R₂) was measured and the percentage detergency calculated according to the following equation: % Detergency = Ks 1 - Ks 2 Ks 1 x 100
    Figure imgb0002
    where Ks 1 = (1- R 1 ) 2 2R 1 and Ks 2 = (1-R 2 ) 2 2R 2
    Figure imgb0003
    The higher the percentage detergency, the greater the soil release benefit.
  • Figure imgb0004
  • Figure imgb0005
  • These results show that known compositions comprising conventional quaternary ammonium compositions (Composition B) show a smaller soil release benefit than compositions according to the invention (Composition A).
  • Example 2
  • Liquid fabric softening compositions as given below were made as described in Example 1. The soil release properties of the compositions were measured as described in Example 1 excepting that the pieces were first rinsed in 1 litre of 14°FH water containing 2ml of either composition.
  • Figure imgb0006
  • These results show that compositions comprising ester-linked quaternaries show a soil release benefit greater than that obtained from compositions comprising conventional quaternary and that the benefit is seen in the absence of a nonionic stabilising agent.
  • Example 3
  • Example 2 was repeated with a composition which did not contain any nonionic to show that the improved soil release benefit is due entirely to the use of the biodegradable ester linked quaternary ammonium compound.
    Figure imgb0007
  • This example clearly demonstrates the superior soil release behaviour of use of the softening composition according to the invention. The difference is statistically significant; P<0.05.

Claims (9)

  1. Use as a soil release agent in a fabric softening composition of at least 1% by weight of a quaternary ammonium material comprising a compound having two C₁₂₋₂₈ alkyl or alkenyl groups connected via an ester link to a hydrocarbon chain which is connected to the quaternary nitrogen atom.
  2. Use of a quaternary ammonium material as claimed in claim 1 wherein the fabric softening composition comprises a nonionic stabilising agent which is
    i. a linear C₈ to C₂₂ alcohol alkoxylated with 10 to 20 moles of alkylene oxide or
    ii. a C₁₀ to C₂₀ alcohol or mixtures thereof.
  3. Use of a quaternary ammonium material as claimed in claim 1 or claim 2 wherein the fabric softening composition comprises a fatty acid material.
  4. Use of a quaternary ammonium material as claimed in claim 2 wherein the composition comprises from 0.1 to 10% by weight of the nonionic stabilising agent.
  5. Use of a quaternary ammonium material as claimed in claim 3 wherein the composition also comprises more than 0.1% by weight of a fatty acid material.
  6. Use of a quaternary ammonium material as claimed in any preceding claim wherein the composition comprises from 3% to 50% by weight of the quaternary ammonium material, from 0.5% to 5% by weight of the nonionic stabilising agent and from 0.5 to 20% by weight of fatty acid material.
  7. Use of a quaternary ammonium material as claimed in any one of claims 2 to 6 wherein the nonionic stabilising agent has an HLB of between 10 and 20.
  8. Use of a quaternary ammonium material as claimed in claim 7 wherein the nonionic stabilising agent has an HLB of between 12 and 20.
  9. Use of a quaternary ammonium material as claimed in any preceding claim wherein the quaternary ammonium material is represented by the formula:
    Figure imgb0008
    wherein R₁ is an alkyl or hydroxyalkyl group containing from 1 to 4 carbon atoms; and R₂ is a C₁₁-C₂₃ alkyl chain.
EP92302453A 1991-03-25 1992-03-20 Use of fabric softening composition Expired - Lifetime EP0506312B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB919106308A GB9106308D0 (en) 1991-03-25 1991-03-25 Fabric softening composition
GB9106308 1991-03-25

Publications (2)

Publication Number Publication Date
EP0506312A1 EP0506312A1 (en) 1992-09-30
EP0506312B1 true EP0506312B1 (en) 1996-01-17

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EP92302453A Expired - Lifetime EP0506312B1 (en) 1991-03-25 1992-03-20 Use of fabric softening composition
EP92302452A Revoked EP0507478B1 (en) 1991-03-25 1992-03-20 Fabric softening composition

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EP92302452A Revoked EP0507478B1 (en) 1991-03-25 1992-03-20 Fabric softening composition

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EP (2) EP0506312B1 (en)
JP (1) JP2937306B2 (en)
AU (1) AU652429B2 (en)
BR (1) BR9201017A (en)
CA (1) CA2063463C (en)
DE (2) DE69207624T2 (en)
ES (2) ES2083084T3 (en)
GB (1) GB9106308D0 (en)
ZA (1) ZA922173B (en)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9115255D0 (en) * 1991-07-15 1991-08-28 Unilever Plc Fabric softening composition
GB9301728D0 (en) * 1993-01-28 1993-03-17 Unilever Plc Fabric softening composition
WO1993023510A1 (en) * 1992-05-12 1993-11-25 The Procter & Gamble Company Concentrated fabric softener compositions containing biodegradable fabric softeners
ES2099451T3 (en) * 1992-06-10 1997-05-16 Procter & Gamble SOFTENING COMPOSITIONS OF STABLE AND BIODEGRADABLE FABRICS.
CN1066188C (en) * 1993-03-01 2001-05-23 普罗格特-甘布尔公司 Concentrated biodegradable quaternary ammonium fabric softener compositions and compounds containing intermediate iodine value unsaturated fatty acid chains
US5750491A (en) * 1993-08-02 1998-05-12 The Procter & Gamble Company Super concentrate emulsions with fabric actives
US6559117B1 (en) 1993-12-13 2003-05-06 The Procter & Gamble Company Viscosity stable concentrated liquid fabric softener compositions
US5413723A (en) * 1993-12-17 1995-05-09 Munteanu; Marina A. Use of special surfactants to control viscosity in fabric softeners
EP0754215B1 (en) * 1994-04-07 2001-05-23 Unilever Plc Fabric softening composition
GB9406824D0 (en) * 1994-04-07 1994-06-01 Unilever Plc Fabric softening composition
AU2399295A (en) * 1994-04-29 1995-11-29 Procter & Gamble Company, The Cellulase fabric-conditioning compositions
MA23554A1 (en) * 1994-05-18 1995-12-31 Procter & Gamble SOFTENING COMPOSITIONS FOR BIODEGRADABLE AND CONCENTRATED QUATERNARY AMMONIUM BASED LAUNDRY CONTAINING QUATERNARY AMMONIUM COMPOUNDS WITH SHORT FATTY ACID ALKYL CHAINS
US5445747A (en) * 1994-08-05 1995-08-29 The Procter & Gamble Company Cellulase fabric-conditioning compositions
US5503756A (en) * 1994-09-20 1996-04-02 The Procter & Gamble Company Dryer-activated fabric conditioning compositions containing unsaturated fatty acid
US5460736A (en) * 1994-10-07 1995-10-24 The Procter & Gamble Company Fabric softening composition containing chlorine scavengers
US5474690A (en) * 1994-11-14 1995-12-12 The Procter & Gamble Company Concentrated biodegradable quaternary ammonium fabric softener compositions containing intermediate iodine value fatty acid chains
GB9503596D0 (en) * 1995-02-23 1995-04-12 Unilever Plc Cleaning composition comprising quaternised poly-dimethylsiloxane and nonionic surfactant
GB9517433D0 (en) * 1995-08-25 1995-10-25 Unilever Plc Soil release agent and its use in fabric conditioning compositions
GB9526182D0 (en) * 1995-12-21 1996-02-21 Unilever Plc Fabric softening composition
GB2313379A (en) * 1996-05-23 1997-11-26 Unilever Plc A detergent composition comprising perfume
BR9701287A (en) * 1997-03-14 1998-11-10 Unilever Nv Fabric treatment composition in washing and process to treat fabrics to provide them with dirt repellent properties
GB0121802D0 (en) 2001-09-10 2001-10-31 Unilever Plc Fabric conditioning compositions
EP1354872A1 (en) 2002-04-17 2003-10-22 Kao Corporation Sulfuric acid ester amine salts, sulfonic acid amine salts, production thereof and softener composition
ATE401385T1 (en) * 2003-10-16 2008-08-15 Procter & Gamble AQUEOUS COMPOSITIONS CONTAINING VESICLES WITH A CERTAIN VESICLE PERMEABILITY
US7655609B2 (en) 2005-12-12 2010-02-02 Milliken & Company Soil release agent
US9926516B2 (en) 2014-06-05 2018-03-27 The Procter & Gamble Company Mono alcohols for low temperature stability of isotropic liquid detergent compositions

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3974076A (en) * 1974-01-11 1976-08-10 The Procter & Gamble Company Fabric softener
GB1567947A (en) * 1976-07-02 1980-05-21 Unilever Ltd Esters of quaternised amino-alcohols for treating fabrics
EP0042187B2 (en) * 1980-06-17 1988-09-28 THE PROCTER &amp; GAMBLE COMPANY Detergent composition containing low level of substituted polyamines
DE3605716A1 (en) * 1986-02-22 1987-09-03 Henkel Kgaa USE OF INSOLUBLE DIRT COLLECTORS FOR REGENERATING WASHING AND CLEANING SOLUTIONS
GB8704711D0 (en) * 1987-02-27 1987-04-01 Unilever Plc Fabric softening composition
US4808321A (en) * 1987-05-01 1989-02-28 The Procter & Gamble Company Mono-esters as fiber and fabric treatment compositions
US4789491A (en) * 1987-08-07 1988-12-06 The Procter & Gamble Company Method for preparing biodegradable fabric softening compositions
EP0309052B1 (en) * 1987-09-23 1992-11-25 The Procter & Gamble Company Stable biodegradable fabric softening compositions containing linear alkoxylated alcohols
GB8804818D0 (en) * 1988-03-01 1988-03-30 Unilever Plc Fabric softening composition
DE3818061A1 (en) * 1988-05-27 1989-12-07 Henkel Kgaa LIQUID, AQUEOUS LAUNDRY TREATMENT AGENT

Also Published As

Publication number Publication date
DE69211203D1 (en) 1996-07-11
EP0506312A1 (en) 1992-09-30
DE69211203T2 (en) 1996-10-10
EP0507478B1 (en) 1996-06-05
DE69207624D1 (en) 1996-02-29
EP0507478A1 (en) 1992-10-07
ES2088542T3 (en) 1996-08-16
BR9201017A (en) 1992-11-24
ZA922173B (en) 1993-09-27
GB9106308D0 (en) 1991-05-08
JPH05106166A (en) 1993-04-27
AU652429B2 (en) 1994-08-25
JP2937306B2 (en) 1999-08-23
DE69207624T2 (en) 1996-05-30
AU1312592A (en) 1992-10-01
CA2063463C (en) 1999-04-27
ES2083084T3 (en) 1996-04-01
CA2063463A1 (en) 1992-09-26

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