EP0280550A2 - Composition adoucissante pour textiles - Google Patents

Composition adoucissante pour textiles Download PDF

Info

Publication number
EP0280550A2
EP0280550A2 EP88301628A EP88301628A EP0280550A2 EP 0280550 A2 EP0280550 A2 EP 0280550A2 EP 88301628 A EP88301628 A EP 88301628A EP 88301628 A EP88301628 A EP 88301628A EP 0280550 A2 EP0280550 A2 EP 0280550A2
Authority
EP
European Patent Office
Prior art keywords
fabric softening
ethoxylated
nonionic surfactant
ethylene oxide
average
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
EP88301628A
Other languages
German (de)
English (en)
Other versions
EP0280550A3 (en
EP0280550B1 (fr
Inventor
Eunice Sheila Blackmore
Brian William Topping
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=10613088&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP0280550(A2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Unilever PLC, Unilever NV filed Critical Unilever PLC
Publication of EP0280550A2 publication Critical patent/EP0280550A2/fr
Publication of EP0280550A3 publication Critical patent/EP0280550A3/en
Application granted granted Critical
Publication of EP0280550B1 publication Critical patent/EP0280550B1/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/327Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated alcohols or esters 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/04Carboxylic acids or 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/86Mixtures of anionic, cationic, and non-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
    • 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
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
    • D06M13/46Compounds containing quaternary nitrogen atoms
    • 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
    • C11D1/662Carbohydrates or derivatives
    • 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
    • C11D1/667Neutral esters, e.g. sorbitan esters
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/72Ethers of polyoxyalkylene glycols
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/74Carboxylates or sulfonates esters of polyoxyalkylene glycols
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/75Amino oxides

Definitions

  • the present invention relates to a fabric softening composition, in particular a fabric softening composition containing a water-insoluble cationic fabric softening agent, a fatty acid and other nonionic surfactants.
  • liquid fabric softening composition comprising
  • the water-insoluble cationic fabric softening agent can be any fabric-substantive cationic compound which has a solubility in water at pH 2.5 and 20°C of less than 10 g/l.
  • Highly preferred materials are quaternary ammonium salts having two C12-C24 alkyl or alkenyl chains, option­ally substituted or interrupted by functional groups such as -OH, -O-, -CONH-, -COO-, etc.
  • R1 and R2 represent hydrocarbyl groups having from about 12 to about 24 carbon atoms
  • R3 and R4 represent hydrocarbyl groups containing from 1 to about 4 carbon atoms
  • X is an anion, preferably selected from halide, methyl sulfate and ethyl sulfate radicals.
  • quaternary softeners include ditallow dimethyl ammonium chloride; ditallow dimethyl ammonium methyl sulfate; dihexadecyl dimethyl ammonium chloride; di(hydrogenated tallow alkyl) dimethyl ammonium chloride; dioctadecyl dimethyl ammonium chloride; dieicosyl dimethyl ammonium chloride; didocosyl dimethyl ammonium chloride; di(hydrogenated tallow) dimethyl ammonium methyl sulfate; dihexadecyl diethyl ammonium chloride; di(coconut alkyl) dimethyl ammonium chloride.
  • dialkyl ethoxyl methyl ammonium sulphates based on soft or hard fatty acids.
  • Ditallow dimethyl ammonium chloride, di(hydrogenated tallow alkyl) dimethyl ammonium chloride, di(coconut alkyl) dimethyl ammonium chloride and di(coconut alkyl) dimethyl ammonium methosulfate are preferred.
  • alkylimidazolinium salts believed to have the formula: wherein R6 is an alkyl or hydroxyalkyl group containing from 1 to 4, preferably 1 or 2 carbon atoms, R7 is an alkyl or alkenyl group containing from 8 to 25 carbon atoms, R8 is an alkyl or alkenyl group containing from 8 to 25 carbon atoms, and R9 is hydrogen or an alkyl containing from 1 to 4 carbon atoms and A ⁇ is an anion, preferably a halide, methosulfate or ethosulfate.
  • Preferred imidazolinium salts include 1-methyl-1-­(tallowylamido-) ethyl -2-tallowyl- 4,5-dihydro imidazo­linium methosulfate and 1-methyl-1- (palmitoylamido)ethyl -2-octadecyl-4,5- dihydro- imidazolinium chloride.
  • Other useful imidazolinium materials are 2-heptadecyl-1-­methyl-1- (2-stearylamido)- ethyl-imidazolinium chloride and 2-lauryl-1-hydroxyethyl- 1-oleyl-imidazolinium chloride.
  • Also suitable herein are the imidazolinium fabric softening components of US Patent No 4 127 489, incorporated by reference. Mixtures of various cationic fabric softening agents can also be used.
  • the level of the cationic fabric softening agent in the composition is preferably more than 1% by weight, most preferably from 3% to 6% by weight.
  • Suitable fatty acids which can be used in the present invention are C8-C24 alkyl or alkenyl linear or branched chain monocarboxylic acids or polymers thereof.
  • Preferably saturated fatty acids are used, in particular, hardened tallow C16-C18 fatty acids. Mixtures of various fatty acids can also be used.
  • the level of the fatty acid in the composition is preferably less than 8% by weight, most preferably from 0.2% to 2.5% by weight.
  • the mole ratio of the cationic fabric softening agent to the fatty acid is at least 1:1, and preferably is within the range 4:1 to 9:1.
  • Suitable nonionic surfactants which can be used include in particular the reaction products of compounds having a hydrophobic group and a reactive hydrogen atom, for example aliphatic alcohols, acids, or alkyl phenols with alkylene oxides, especially ethylene oxide either alone or with propylene oxide.
  • Specific nonionic surfactants are alkyl (C6-C22) phenols-ethylene oxide condensates, generally up to 25 EO, ie up to 25 units of ethylene oxide per molecule, the condensation products of aliphatic (C8-C22) primary or secondary linear or branched alcohols with ethylene oxide, generally up to 40 EO, and products made by condensation of ethylene oxide with the reaction products of propylene oxide and ethylenediamine.
  • Other so-called nonionic surfactants include amine oxides, alkyl polyglycosides, ethoxylated castor oils, and sorbitan esters.
  • the level of the nonionic surfactant is within the range from 0.1 to 4.5% by weight, most preferably from 0.15% to 3% by weight.
  • the mole ratio of the cationic fabric softening agent to the nonionic surfactant 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 one or more optional ingredients selected from non-aqueous solvents such as C1-C4 alkanols and polyhydric alcohols (although the benefits of this invention can be obtained without the addition of these materials), pH buffering agents, such as weak acids eg phosphoric, benzoic or citric acids (the pH of the compositions are preferably less than 6.0), rewetting agents, viscosity modifiers, such as electrolytes and C9-C24 fatty acids included at levels from about 20 to 6000 ppm, antigelling agents, perfumes, perfume carriers, fluorescers, colourants, hydrotropes, antifoaming agents, antiredeposition agents, enzymes, optical brightening agents, opacifiers, stabilisers such as guar gum and polyethylene glycol, anti-shrinking agents, anti-wrinkle agents, fabric crisping agents, anti-spotting agents, soil-release agents, germicides, fungicides, anti-oxidants, anti-corrosion agents, preservatives such
  • Suitable silicones for use in the compositions according to the invention include predominantly linear polydialkyl or alkylaryl siloxanes in which the alkyl groups contain one to five carbon atoms.
  • the siloxanes can be amido or amino substituted.
  • the siloxane is amine substituted the amine group may be quaternised.
  • compositions may also contain, in addition to the cationic fabric softening agent, other non-cationic fabric softening agents, such as nonionic fabric softening agents.
  • Suitable nonionic fabric softening agents include lanolin and derivatives thereof. Suitable materials are disclosed in European Patent Applications 88 520 (Unilever), the disclosure of which is incorporated herein by reference. Typically such materials are included at a level within the range of from 0.5% to 10% by weight of the composition.
  • the fabric conditioning composition of the invention may be added to a large volume of water to form a liquor with which the fabrics to be treated are contacted.
  • the total concentration of the cationic fabric softening agent, the fatty acid and the nonionic surfactant in this liquor will be between about 30 ppm and 500 ppm.
  • the weight ratio of the fabrics to liquor will preferably be less than about 25:1, most preferably between about 10:1 and about 4:1.
  • compositions of the invention may be prepared by a variety of methods.
  • One suitable method is to form a molten mixture of the cationic fabric softening agent and the fatty acid, add this molten mixture to water with stirring to form a dispersion and thereafter add the nonionic surfactant and any optional ingredients.
  • Another suitable method is to add the nonionic surfactant to the molten mixture before the dispersion is formed.
  • a liquid fabric softening composition was made as follows.
  • the cationic fabric softening agent and the fatty acid were premixed and heated together until clear (60-75°C).
  • the molten mixture thus formed was added over a period of at least one minute, via a dip pipe, to water at 45-60°C, with constant stirring to form a dispersion.
  • Other minor ingredients including perfume were added with constant stirring whilst the temperature of the dispersion was greater than 35°C.
  • the nonionic surfactant was most preferably added after the mixture had cooled to 35°C or below.
  • Example 1 was repeated except that the Nonidet LE 6T was excluded from the composition (Example 1A).
  • a freeze thaw cycle in this context involves storing 100g of product in a screw-capped polyethylene bottle for 16 hours at a temperature of -12°C or less. Such low temperatures are essential to ensure that the products are completely frozen. The product is then allowed to thaw at ambient temperatures for 8 hours.
  • Example 1 After 1 freeze thaw cycle Example 1 gave a composition which was slightly thicker than normal. After 3 and 6 freeze thaw cycles Example 1 gave a composition which had normal rinse conditioner rheology ie. was mobile and could be poured in a continuous stream. Example 1A after 1, 3 and 6 freeze thaw cycles gave a composition which was just mobile but which did not pour in a continuous stream.
  • Example 2L For comparison purposes a composition containing no nonionic (Example 2L) was prepared and tested. In Example 2A a level of APG 300 of 0.2% rather than 0.4% was used. Each composition was subjected to the following cap dispenser test after 1 and 3 freeze thaw cycles.
  • Products were allowed to recover from freezing and a known amount (usually 20 grams) was weighed into an internally screw threaded cap with a total capacity of approximately 25 cm3 and of known weight. The cap was then inverted over a waste container for 10 seconds and re-weighed. The results obtained are expressed as a percentage of the amount of product weighed into the cap. Prior to freezing, the samples were found to leave up to approximately 10% residue in the cap.
  • Nonidet LE6T is replaced by Tween 20, Alfol 1214-7, Alfol 1214-11, Alfol 1214-13, Brij 30, Brij 35, Lutensol AO7, Lutensol AO8, and Synperonic A11.
  • This example demonstrates the effect of increasing levels of nonionic surfactant on the freeze-thaw stability of a 4.2% active with a ratio of Arquad 2HT:Pristerene 4916 of 6:1 by weight and a perfume level of 0.13%.
  • the compositions were prepared by the method previously described.
  • the levels of nonionic are expressed in terms of wt% of the final formulation.
  • the products were assessed after one freeze thaw cycle via the cap dispenser test described above.
  • This example demonstrates the effect of low levels of Nonidet LE 6T on formulations other than those containing 4.2% active and a 6:1 weight ratio of cationic fabric softening agent to fatty acid.
  • the compositions were prepared as described above and the percentage ingredient refers to their weight % in the final product.
  • compositions were evaluated according to the cap dispenser test as described above.
  • compositions with the following formulations were prepared as described above. Once again the amount of each ingredient refers to weight % in the final product composition.
  • compositions were assessed visually after recovery from 1 freeze thaw cycle.
  • addition of a nonionic surfactant improved the appearance and flow characteristics of the composition.
  • This Example demonstrates that the beneficial effect of adding nonionic surfactant is not restricted to compositions containing Arquad 2HT and Pristerene 4916.
  • the softening performance was assessed after one freeze/thaw cycle by subjective evaluation by a panel of expert graders.
  • compositions were dispersed in tap water to give dilute aqueous dispersions containing 0.01% of active ingredients.
  • Four pieces of cotton towelling 50 grams were rinsed in a tergotometer with one litre of the aqueous dispersion at ambient temperature for 5 minutes.
  • compositions were found to give a similar softening benefit. However, after one freeze/thaw cycle the composition containing no nonionic surfactant (Example 6B) was just mobile but did not pour in a continous stream whereas the composition according to the invention was slightly thicker than normal rinse conditioner rheology but could still be poured in a continuous stream.
  • Alfol 1214-7 C12-C14 straight chain alcohol (with an even number of carbon atoms), ethoxylated with an average of 7 ethylene oxide groups per molecule.
  • Alfol 1214-11 As Alfol 1214-7, but with an average of 11 ethylene oxide groups per molecule.
  • Alfol 1214-13 As Alfol 1214-7, but with an average of 13 ethylene oxide groups per molecule.
  • APG 300 Alkyl Polyglycoside based on a C9-C11 alcohol and having an average of 1.6 glycosidic rings per mole of alcohol (supplied as a 51% active solution).
  • Arquad 2HT Commercially available form of dihardened tallow dimethyl ammonium chloride (DMDHTAC)(supplied as a 75% active paste).
  • Brij 30 C12-C14 straight chain alcohol (with an even number of carbon atoms and of natural origin) ethoxylated with an average of 4 ethylene oxide groups per molecule.
  • Brij 35 As Brij 30, but with an average of 23 ethylene oxide groups per molecule.
  • DMC AO Dimethyl coco amine oxide supplied as 30% solution.
  • Dobanol 91-6 C9-C11 branched chain primary alcohol, ethoxylated with an average of 6 ethylene oxide groups per molecule.
  • Dobanol 45-18 C14-C15 branched chain alcohol, ethoxylated with an average of 18 ethylene oxide groups per molecule.
  • Etocas 35 Castor oil ethoxylated with an average of 35 ethylene oxide groups per molecule.
  • Genapol 0-050 Oleyl alcohol ethoxylated with an average of 50 ethylene oxide groups per molecule.
  • Genapol 0-200 Oleyl alcohol ethoxylated with an average of 200 ethylene oxide groups per molecule.
  • Lutensol OA7 C13-C15 branched chain alcohol ethoxylated with an average of 7 ethylene oxide groups per molecule.
  • Lutensol OA8 As Lutensol OA7, but with an average of 8 ethylene oxide groups per molecule.
  • Nonidet LE 6T Similar material to Dobanol 91-6 except that it is topped to remove volatile materials.
  • Nonyl phenol 20EO Nonylphenol ethoxylated with 20 ethylene oxide groups per molcule.
  • Pristerene 4916 Commercially available form of hardened tallow fatty acid (HTFA).
  • Span 20 Sorbitan monolaurate.
  • Stepantex Q185 A dialkylethoxymethyl ammonium methosulphate based on soft fatty acid.
  • Stepantex VP85 A dialkylethoxymethyl ammonium methosulphate based on hard fatty acid.
  • Synperonic All C13-C15 branched chain alcohol ethoxylated with an average of 11 ethylene oxide groups per molecule.
  • Tergitol 15-S-7 C11-C15 secondary alcohol ethoxylated with an average of 7 ethylene oxide groups per molecule.
  • Tween 20 Polyoxyethylene sorbitan monolaurate containing 20 ethylene oxide groups per molecule.
  • Tween 20/Span 20 A 50/50 weight % mixture. (50:50)
  • Varisoft 222 Diamidoquaternary based on soft tallow.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Textile Engineering (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
EP19880301628 1987-02-27 1988-02-25 Composition adoucissante pour textiles Expired - Lifetime EP0280550B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB878704711A GB8704711D0 (en) 1987-02-27 1987-02-27 Fabric softening composition
GB8704711 1987-02-27

Publications (3)

Publication Number Publication Date
EP0280550A2 true EP0280550A2 (fr) 1988-08-31
EP0280550A3 EP0280550A3 (en) 1989-03-29
EP0280550B1 EP0280550B1 (fr) 1990-10-24

Family

ID=10613088

Family Applications (1)

Application Number Title Priority Date Filing Date
EP19880301628 Expired - Lifetime EP0280550B1 (fr) 1987-02-27 1988-02-25 Composition adoucissante pour textiles

Country Status (12)

Country Link
EP (1) EP0280550B1 (fr)
JP (1) JPS63282373A (fr)
KR (1) KR910009652B1 (fr)
AU (1) AU614073B2 (fr)
BR (1) BR8800833A (fr)
CA (1) CA1291302C (fr)
DE (1) DE3860842D1 (fr)
ES (1) ES2018338B3 (fr)
GB (1) GB8704711D0 (fr)
MY (1) MY103215A (fr)
TR (1) TR24515A (fr)
ZA (1) ZA881382B (fr)

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0354011A1 (fr) * 1988-08-04 1990-02-07 Albright & Wilson Limited Agents de conditionnement pour le linge
WO1992019714A1 (fr) * 1991-04-30 1992-11-12 The Procter & Gamble Company Produits assouplissants contenant de l'imidazoline substituee et des composes fortement ethoxyles
WO1993024603A2 (fr) * 1992-06-02 1993-12-09 Unilever N.V. Produits de nettoyage liquides
US5409621A (en) * 1991-03-25 1995-04-25 Lever Brothers Company, Division Of Conopco, Inc. Fabric softening composition
US5484540A (en) * 1991-03-08 1996-01-16 The Procter & Gamble Company Concentrated fabric softening compositions
US5503756A (en) * 1994-09-20 1996-04-02 The Procter & Gamble Company Dryer-activated fabric conditioning compositions containing unsaturated fatty acid
US5773409A (en) * 1994-04-07 1998-06-30 Lever Brothers Company, Division Of Conopco, Inc. Fabric softening composition
AU696570B2 (en) * 1995-03-01 1998-09-10 Colgate-Palmolive Company, The Laundry concentrates
EP1028161A1 (fr) * 1999-02-12 2000-08-16 Kao Corporation Détergent et son utilisation
WO2001046363A1 (fr) * 1999-12-22 2001-06-28 Unilever Plc Procede de preparation de compositions d'adoucissement de textiles
EP1290124B2 (fr) 2000-06-16 2007-01-03 Unilever Plc Compositions adoucissantes pour tissus
WO2012072368A1 (fr) 2010-12-03 2012-06-07 Unilever Plc Conditionneurs de tissu
WO2012072369A1 (fr) 2010-12-03 2012-06-07 Unilever Plc Conditionneurs de tissu
WO2018044639A1 (fr) * 2016-08-31 2018-03-08 The Procter & Gamble Company Composition d'amélioration de tissus

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8914054D0 (en) * 1989-06-19 1989-08-09 Unilever Plc Fabric softening composition
JP2641110B2 (ja) * 1990-12-19 1997-08-13 大日精化工業株式会社 柔軟仕上げ剤組成物
GB9115255D0 (en) * 1991-07-15 1991-08-28 Unilever Plc Fabric softening composition
GB9106308D0 (en) * 1991-03-25 1991-05-08 Unilever Plc Fabric softening composition
KR100591100B1 (ko) * 2000-06-26 2006-06-19 주식회사 코오롱 열가소성 합성섬유용 유제 조성물
ES2524401T3 (es) 2010-10-22 2014-12-09 Unilever N.V. Mejoras relacionadas con acondicionadores de tejidos
EP2646536B1 (fr) 2010-12-03 2015-01-07 Unilever PLC Adjuvants adoucissants pour le linge
US20190264136A1 (en) * 2018-02-28 2019-08-29 The Procter & Gamble Company Fabric enhancer composition

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2822891A1 (de) * 1977-05-30 1978-12-07 Procter & Gamble Europ Textilbehandlungsmittel
FR2440433A1 (fr) * 1978-11-03 1980-05-30 Unilever Nv Composition d'assouplissement des etoffes et procede pour la preparer
EP0013780A1 (fr) * 1979-01-11 1980-08-06 THE PROCTER & GAMBLE COMPANY Composition concentrée d'adoucissement pour tissus
EP0082457A2 (fr) * 1981-12-18 1983-06-29 Hoechst Aktiengesellschaft Agents concentrés adoucissant le linge
EP0122141A2 (fr) * 1983-04-08 1984-10-17 Unilever Plc Compositions adoucissantes pour matières textiles
EP0123999A2 (fr) * 1983-04-22 1984-11-07 Henkel Kommanditgesellschaft auf Aktien Concentré pour adoucissage de textiles confectionnés

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2822891A1 (de) * 1977-05-30 1978-12-07 Procter & Gamble Europ Textilbehandlungsmittel
FR2440433A1 (fr) * 1978-11-03 1980-05-30 Unilever Nv Composition d'assouplissement des etoffes et procede pour la preparer
EP0013780A1 (fr) * 1979-01-11 1980-08-06 THE PROCTER & GAMBLE COMPANY Composition concentrée d'adoucissement pour tissus
EP0082457A2 (fr) * 1981-12-18 1983-06-29 Hoechst Aktiengesellschaft Agents concentrés adoucissant le linge
EP0122141A2 (fr) * 1983-04-08 1984-10-17 Unilever Plc Compositions adoucissantes pour matières textiles
EP0123999A2 (fr) * 1983-04-22 1984-11-07 Henkel Kommanditgesellschaft auf Aktien Concentré pour adoucissage de textiles confectionnés

Cited By (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0354011A1 (fr) * 1988-08-04 1990-02-07 Albright & Wilson Limited Agents de conditionnement pour le linge
US5484540A (en) * 1991-03-08 1996-01-16 The Procter & Gamble Company Concentrated fabric softening compositions
US5409621A (en) * 1991-03-25 1995-04-25 Lever Brothers Company, Division Of Conopco, Inc. Fabric softening composition
US5670476A (en) * 1991-04-30 1997-09-23 The Procter & Gamble Company Fabric softening compositions containing mixtures of substituted imidazoline fabric softener materials and highly ethoxylated curd dispersant
WO1992019714A1 (fr) * 1991-04-30 1992-11-12 The Procter & Gamble Company Produits assouplissants contenant de l'imidazoline substituee et des composes fortement ethoxyles
WO1993024603A2 (fr) * 1992-06-02 1993-12-09 Unilever N.V. Produits de nettoyage liquides
WO1993024603A3 (fr) * 1992-06-02 1994-03-17 Unilever Plc Produits de nettoyage liquides
US5378387A (en) * 1992-06-02 1995-01-03 Lever Brothers Company, Division Of Conopco, Inc. Non-aqueous liquid cleaning products comprising polyalkoxylated derivatives of castor oil ricinoleic acid and analogous fatty alcohols
US5773409A (en) * 1994-04-07 1998-06-30 Lever Brothers Company, Division Of Conopco, Inc. Fabric softening composition
US5578234A (en) * 1994-09-20 1996-11-26 The Procter & Gamble Company Dryer-activated fabric conditioning compositions containing unsaturated fatty acid
US5503756A (en) * 1994-09-20 1996-04-02 The Procter & Gamble Company Dryer-activated fabric conditioning compositions containing unsaturated fatty acid
AU696570B2 (en) * 1995-03-01 1998-09-10 Colgate-Palmolive Company, The Laundry concentrates
US5856287A (en) * 1995-03-01 1999-01-05 Colgate-Palmolive Co. Laundry concentrates
EP1028161A1 (fr) * 1999-02-12 2000-08-16 Kao Corporation Détergent et son utilisation
US6221828B1 (en) 1999-02-12 2001-04-24 Kao Corporation Detergent composition comprising an alkylpolyglycoside, a germicide, and a fatty acid salt
WO2001046363A1 (fr) * 1999-12-22 2001-06-28 Unilever Plc Procede de preparation de compositions d'adoucissement de textiles
EP1290124B2 (fr) 2000-06-16 2007-01-03 Unilever Plc Compositions adoucissantes pour tissus
WO2012072368A1 (fr) 2010-12-03 2012-06-07 Unilever Plc Conditionneurs de tissu
WO2012072369A1 (fr) 2010-12-03 2012-06-07 Unilever Plc Conditionneurs de tissu
WO2018044639A1 (fr) * 2016-08-31 2018-03-08 The Procter & Gamble Company Composition d'amélioration de tissus
US10487292B2 (en) 2016-08-31 2019-11-26 The Procter & Gamble Company Fabric enhancer composition

Also Published As

Publication number Publication date
KR880010184A (ko) 1988-10-07
GB8704711D0 (en) 1987-04-01
ZA881382B (en) 1989-10-25
TR24515A (tr) 1991-11-12
JPS63282373A (ja) 1988-11-18
BR8800833A (pt) 1988-10-04
AU1206788A (en) 1988-09-01
MY103215A (en) 1993-05-29
ES2018338B3 (es) 1991-04-01
EP0280550A3 (en) 1989-03-29
EP0280550B1 (fr) 1990-10-24
AU614073B2 (en) 1991-08-22
CA1291302C (fr) 1991-10-29
KR910009652B1 (ko) 1991-11-25
DE3860842D1 (de) 1990-11-29

Similar Documents

Publication Publication Date Title
EP0280550B1 (fr) Composition adoucissante pour textiles
EP0122141B1 (fr) Compositions adoucissantes pour matières textiles
EP0056695B2 (fr) Compositions pour le traitement de matières textiles
US4222905A (en) Laundry detergent compositions having enhanced particulate soil removal performance
US4260529A (en) Detergent composition consisting essentially of biodegradable nonionic surfactant and cationic surfactant containing ester or amide
CA1340425C (fr) Compositions assouplissantes stables biodegradables pour tissus, a base d'alcools alcoxyles lineaires
EP0199383B1 (fr) Composition pour le traitement de matières textiles
EP0060003B1 (fr) Compositions pour le traitement de matières textiles et leur préparation
US5093014A (en) Fabric treatment composition and the preparation thereof
EP0506312B1 (fr) Utilisation d'adoucissant pour le linge
CA1313675C (fr) Monoesters utilises pour des composes adoucisseurs de fibres et tissus
US4622154A (en) Aqueous fabric softening composition
US4556502A (en) Liquid fabric-softening composition
CA2024699C (fr) Adoucissant pour textiles
AU679483B2 (en) Fabric softener composition
CA1232709A (fr) Assouplissant aqueux concentre pour tissus
CA1232415A (fr) Assouplissant aqueux concentre pour tissus
CA1118314A (fr) Detergent de lessive a proprietes nettoyantes et assouplissantes ameliorees pour tissus
US6927202B2 (en) Fabric conditioning compositions
CA1129299A (fr) Detergent de lessive a capacites ameliorees de nettoyage et de captage des saletes
CA1226407A (fr) Assouplisseur de tissus en solution aqueuse
CA1109754A (fr) Composes detersifs a rendement de detachage ameliore
CA1111060A (fr) Agents tensio-actifs cationiques biodegradables
GB2157726A (en) Aqueous fabric softening 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: A2

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

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

AK Designated contracting states

Kind code of ref document: A3

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

17P Request for examination filed

Effective date: 19890220

17Q First examination report despatched

Effective date: 19890721

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

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

REF Corresponds to:

Ref document number: 3860842

Country of ref document: DE

Date of ref document: 19901129

ET Fr: translation filed
ITF It: translation for a ep patent filed

Owner name: JACOBACCI & PERANI S.P.A.

PLBI Opposition filed

Free format text: ORIGINAL CODE: 0009260

26 Opposition filed

Opponent name: HENKEL KOMMANDITGESELLSCHAFT AUF AKTIEN

Effective date: 19910718

NLR1 Nl: opposition has been filed with the epo

Opponent name: HENKEL KOMMANDITGESELLSCHAFT AUF AKTIEN

RAP4 Party data changed (patent owner data changed or rights of a patent transferred)

Owner name: UNILEVER N.V.

Owner name: UNILEVER PLC

ITTA It: last paid annual fee
PLBN Opposition rejected

Free format text: ORIGINAL CODE: 0009273

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

Free format text: STATUS: OPPOSITION REJECTED

27O Opposition rejected

Effective date: 19930214

NLR2 Nl: decision of opposition
EAL Se: european patent in force in sweden

Ref document number: 88301628.9

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

Ref country code: CH

Payment date: 19970129

Year of fee payment: 10

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

Ref country code: SE

Payment date: 19980116

Year of fee payment: 11

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

Ref country code: NL

Payment date: 19980218

Year of fee payment: 11

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

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19980228

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19980228

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: SE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19990226

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

Ref country code: NL

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19990901

EUG Se: european patent has lapsed

Ref document number: 88301628.9

REG Reference to a national code

Ref country code: GB

Ref legal event code: IF02

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

Ref country code: GB

Payment date: 20070223

Year of fee payment: 20

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

Ref country code: ES

Payment date: 20070226

Year of fee payment: 20

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

Ref country code: DE

Payment date: 20070330

Year of fee payment: 20

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

Ref country code: IT

Payment date: 20070523

Year of fee payment: 20

REG Reference to a national code

Ref country code: GB

Ref legal event code: PE20

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

Ref country code: FR

Payment date: 20070221

Year of fee payment: 20

REG Reference to a national code

Ref country code: ES

Ref legal event code: FD2A

Effective date: 20080226

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

Ref country code: GB

Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION

Effective date: 20080224

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

Ref country code: ES

Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION

Effective date: 20080226