EP0811679B1 - Fabric softening compositions - Google Patents

Fabric softening compositions Download PDF

Info

Publication number
EP0811679B1
EP0811679B1 EP96870068A EP96870068A EP0811679B1 EP 0811679 B1 EP0811679 B1 EP 0811679B1 EP 96870068 A EP96870068 A EP 96870068A EP 96870068 A EP96870068 A EP 96870068A EP 0811679 B1 EP0811679 B1 EP 0811679B1
Authority
EP
European Patent Office
Prior art keywords
fabric softening
alkyl
weight
dye fixing
cationic
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
EP96870068A
Other languages
German (de)
French (fr)
Other versions
EP0811679A1 (en
Inventor
Bruno Albert Jean Hubesch
Alex Masschelein (Nmn)
Ingrid Maria Simonne Sannen
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.)
Procter and Gamble Co
Original Assignee
Procter and Gamble Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to ES96870068T priority Critical patent/ES2200047T3/en
Application filed by Procter and Gamble Co filed Critical Procter and Gamble Co
Priority to EP96870068A priority patent/EP0811679B1/en
Priority to DE69628285T priority patent/DE69628285T2/en
Priority to AU32874/97A priority patent/AU3287497A/en
Priority to CN97197016A priority patent/CN1093878C/en
Priority to CZ983945A priority patent/CZ394598A3/en
Priority to CA002257201A priority patent/CA2257201A1/en
Priority to BR9709634A priority patent/BR9709634A/en
Priority to PCT/US1997/008966 priority patent/WO1997046651A1/en
Priority to JP50065098A priority patent/JP3784417B2/en
Priority to ARP970102382A priority patent/AR007374A1/en
Publication of EP0811679A1 publication Critical patent/EP0811679A1/en
Application granted granted Critical
Publication of EP0811679B1 publication Critical patent/EP0811679B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3703Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3723Polyamines or polyalkyleneimines
    • 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
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/0021Dye-stain or dye-transfer inhibiting compositions

Definitions

  • the present invention relates to fabric softening compositions and more particularly to compositions which reduce the amount of dyes released from coloured fabrics upon wet treatment such as those which occur in a laundry operation.
  • the domestic treatment of coloured fabrics is a problem known in the art to the formulator of laundry compositions. More particularly, the problem of formulating laundry compositions which reduce the amount of dyes released from coloured fabrics upon wet treatment is a particular challenge to the formulator. This problem is now even more acute with the trends of consumer to move towards more colored fabrics.
  • a liquid composition comprising a cationic fabric softener having at least two long chains, a cationic dye fixing agent in amount of 0.1% to 10% by weight, said composition being free of detergent materials, fulfills such a need.
  • detergent materials encompasses detergent surfactant materials selected from soaps, non-soap anionic, nonionic, zwitterionic and amphoteric synthetic and natural detergent surfactants which are not softeners. Not included by this definition are the fatty acids which are fabric softeners, contrary to said soaps components which do not have fabric softener properties.
  • the present invention relates to a liquid fabric softening composition
  • a liquid fabric softening composition comprising a cationic fabric softener having at least two long chains as defined in claim 1 and a cationic dye fixing agent in amount of 0.1% to 10% by weight, said composition being free of detergent materials.
  • a method for treating fabrics comprises contacting the fabrics during the rinse cycle of a consumer laundry process with an aqueous medium containing at least 50 ppm of a fabric softening composition of the invention.
  • An essential component of the invention is a cationic fabric softener component having at least two long chains as defined in claim 1.
  • component having at least two long chains is meant a component containing at least two alkyl or alkenyl chains, each comprising from 10 to 25 carbon atoms.
  • Such fabric softener provides effective softness benefit to the treated fabrics.
  • Typical levels of said fabric softener components within the liquid softener compositions are from 1% to 80% by weight of the compositions. Depending on the composition execution which can be dilute with a preferred level of fabric softening components from 1% to 5%, or concentrated, with a preferred level of fabric softening components from 5% to 80%, more preferably 10% to 50%, most preferably 15% to 35% by weight.
  • Typical cationic fabric softening components as defined in claim 1 having at least two long chains include the water-insoluble quaternary-ammonium fabric softening actives, the most commonly used having been di-long alkyl chains ammonium chloride.
  • the quaternary ammonium compounds and amine precursors herein have the formula (I) or (II), below: wherein Q is selected from -O-C(O)-, -C(O)-O-, -O-C(O)-O-, -NR 4 -C(O)-, -C(O)-NR 4 -; R 1 is (CH 2 ) n -Q-T 2 or T 3 ; R 2 is (CH 2 ) m -Q-T 4 or T 5 or R 3 ; R 3 is C 1 -C 4 alkyl or C 1 -C 4 hydroxyalkyl or H; R 4 is H or C 1 -C 4 alkyl or C 1 -C 4 hydroxyalkyl; T 1 , T 2 , T 3 , T 4 , T 5 are independently C 11 -C 22 alkyl or alkenyl; n and m are integers from 1 to 4; and X - is a softener-compatible anion.
  • Non-limiting examples of softener-compatible anions include chloride or methyl sulfate.
  • the alkyl, or alkenyl, chain T 1 , T 2 , T 3 , T 4 , T 5 must contain at least 11 carbon atoms, preferably at least 16 carbon atoms.
  • the chain may be straight or branched.
  • Tallow is a convenient and inexpensive source of long chain alkyl and alkenyl material.
  • the compounds wherein T 1 , T 2 , T 3 , T 4 , T 5 represents the mixture of long chain materials typical for tallow are particularly preferred.
  • quaternary ammonium compounds suitable for use in the aqueous fabric softening compositions herein include:
  • compounds 1-8 are examples of compounds of Formula (I); compound 9 is a compound of Formula (II). Particularly preferred is N,N-di(tallowoyl-oxy-ethyl)-N,N-dimethyl ammonium chloride, where the tallow chains are at least partially unsaturated.
  • the level of unsaturation of the tallow chain can be measured by the Iodine Value (IV) of the corresponding fatty acid, which in the present case should preferably be in the range of from 5 to 100 with two categories of compounds being distinguished, having a IV below or above 25.
  • the anion is merely present as a counterion of the positively charged quaternary ammonium compounds.
  • the nature of the counterion is not critical at all to the practice of the present invention. The scope of this invention is not considered limited to any particular anion.
  • amine precursors thereof' is meant the secondary or tertiary amines corresponding to the above quaternary ammonium compounds, said amines being substantially protonated in the present compositions due to the pH values.
  • the pH of the compositions herein is an essential parameter of the present invention. Indeed, it influences the stability of the quaternary ammonium or amine precursors compounds, especially in prolonged storage conditions.
  • the pH as defined in the present context, is measured in the neat compositions at 20°C.
  • the neat pH measured in the above-mentioned conditions, must be in the range of from 2.0 to 4.5.
  • the pH of the neat composition is in the range of 2.0 to 3.0.
  • the pH of these compositions herein can be regulated by the addition of a Bronsted acid.
  • Suitable adds include the inorganic mineral acids, carboxylic acids, in particular the low molecular weight (C 1 -C 5 ) carboxylic acids, and alkylsulfonic acids.
  • Suitable inorganic acids include HCI, H 2 SO 4 , HNO 3 and H 3 PO 4 .
  • Suitable organic acids include formic, acetic, citric, methylsulfonic and ethylsulfonic acid.
  • Preferred acids are citric, hydrochloric, phosphoric, formic, methylsulfonic acid, and benzoic acids.
  • the other essential component of the invention is a cationic dye fixative agent.
  • Cationic dye fixing agents or "fixatives” are well-known, commercially available materials which are designed to improve the appearance of dyed fabric by minimizing the loss of dye from fabrics due to washing.
  • Cationic dye fixatives are based on various quaternized or otherwise cationically charged organic nitrogen compounds. Cationic fixatives are available under various trade names from several suppliers. Representative examples include: CROSCOLOR PMF (July 1981, Code No. 7894) and CROSCOLOR NOFF (January 1988, Code No. 8544) from Crosfield; INDOSOL E-50 (February 27, 1984, Ref. No.
  • Dye fixing agents suitable for use in the present invention are ammonium compounds such as fatty acid - diamine condensates e.g.
  • the amount of dye fixing agent to be employed in the composition of the invention is in amount of from 0.1% to 10% by weight of the composition, preferably from 0.5% to 8% by weight, more preferably from 0.8% to 5.5% by weight of the composition.
  • the weight ratio of fabric softener to dye fixing agent is of from 60:1 to 1.5:1, more preferably from 20:1 to 3.5:1, most preferably from 10:1 to 3.5:1.
  • detergent materials encompasses detergent surfactant materials selected from soaps, non-soap anionic, nonionic, zwitterionic and amphoteric synthetic and natural detergent surfactants which are not softeners. Not included by this definition are the fatty acids which are fabric softeners, contrary to said soaps components which do not have fabric softener properties.
  • Soaps and non-soaps anionic materials are the linear and branched primary alkyl sulfates, alkyl ethoxysulfates, fatty oleyl glycerol sulfates, alkyl phenol ethylene oxide ether sulfates, the C5-C17 acyl-N-(C1-C4 alkyl) and -N-(C1-C2 hydroxyalkyl) glucamine sulfates, and sulfates of alkylpolysaccharides; anionic sulfonate surfactants such as the salts of C5-C20 linear alkylbenzene sulfonates, alkyl ester sulfonates, C6-C22 primary or secondary alkane sulfonates, C6-C24 olefin sulfonates, sulfonated polycarboxylic acids, alkyl glycerol sulfonates,
  • Nonionic detergent materials are the polyhydroxy fatty acid amides, polyethylene, polypropylene, and polybutylene oxide condensates of alkyl phenols; alkyl ethoxylate condensation products of aliphatic alcohols with from about 1 to about 25 moles of ethylene oxide; ethoxylated C 6 -C 18 fatty alcohols and C 6 -C 18 mixed ethoxylated/propoxylated fatty alcohols; alkylpolysaccharides and the fatty acid amides.
  • Zwiterrionic and amphoteric materials are the amine oxides, the alkyl amphocarboxylic acids, the betaines such as coconut acylamidopropyldimethyl betaine and hexadecyl dimethyl betaine.
  • composition may also optionally contain additional components such as additional fabric softener materials, electrolyte concentration aids, stabilisers, such as well known antioxidants and reductive agents, soil release polymers, bacteriocides, colorants, perfumes, preservatives, optical brighteners, anti ionisation agents, antifoam agents and chelating agents.
  • Additional fabric softening materials may be used in addition to the di-long chain cationic fabric softener. When used, such additional fabric softening materials will typically be present in an amount of from 0 to 15% by weight of the composition. Such materials are the single long chain alkyl cationic softeners and/or the fatty acids.
  • Such mono-long-chain-alkyl cationic softeners suitable for use herein are, preferably, quaternary ammonium salts of the general formula [R 2 N + R 3 ] X - wherein the R 2 group is C 10 -C 22 hydrocarbon group, preferably C 12 -C 18 alkyl group of the corresponding ester linkage interrupted group with a short alkylene (C 1 -C 4 ) group between the ester linkage and the N, and having a similar hydrocarbon group, e.g., a fatty acid ester of choline, preferably C 12 -C 14 (coco) choline ester and/or C 16 -C 18 tallow choline ester at from 0.1% to 20% by weight of the softener active.
  • R 2 group is C 10 -C 22 hydrocarbon group, preferably C 12 -C 18 alkyl group of the corresponding ester linkage interrupted group with a short alkylene (C 1 -C 4 ) group between the ester link
  • Each R 3 is a C 1 -C 4 alkyl or substituted (e.g., hydroxy) alkyl, or hydrogen, preferably methyl, and the counterion X - is a softener compatible anion, for example, chloride, bromide, methyl sulfate, etc.
  • Other cationic materials with ring structures such as alkyl imidazoline, imidazolinium, pyridine, and pyridinium salts having a single C 12 -C 30 alkyl chain can also be used. Very low pH is required to stabilize, e.g., imidazoline ring structures.
  • alkyl imidazolinium salts and their imidazoline precursors useful in the present invention have the general formula : wherein Y 2 is -C(O)-O-, -O-(O)C-, -C(O)-N(R 5 )-, or -N(R 5 )-C(O)- in which R 5 is hydrogen or a C 1 -C 4 alkyl radical; R 6 is a C 1 -C 4 alkyl radical or H (for imidazoline precursors); R 7 and R 8 are each independently selected from R 3 and R 2 as defined hereinbefore for the single-long-chain cationic surfactant with only one being R 2 .
  • alkyl pyridinium salts useful in the present invention have the general formula: wherein R 2 and X- are as defined above.
  • a typical material of this type is cetyl pyridinium chloride.
  • Suitable fatty acids include those containing from 10 to 25, preferably from 12 to 25 total carbon atoms, with the fatty moiety containing from 10 to 22, preferably from 16 to 22, carbon atoms.
  • the shorter moiety contains from 1 to 4, preferably from 1 to 2 carbon atoms.
  • the level of unsaturation of the tallow chain can be measured by the Iodine Value (IV) of the corresponding fatty acid, which in the present case should preferably be in the range of from 5 to 100, more preferably in the range of from 0 to 25.
  • fatty acid compounds suitable for use in the liquid fabric softening compositions herein include compounds selected from lauric acid, myristic acid, palmitic acid, stearic acid, arachidic acid, behenic acid, oleic acid, coconut fatty acid, tallow fatty acid, partially hydrogenated tallow fatty acid and mixtures thereof.
  • a most preferred fatty acid compound is tallow fatty acid with an Iodine Value (IV) of 18.
  • the fatty acid When the above mentioned fatty acids are used, the fatty acid will be present in a weight ratio of said cationic fabric softening agents having di-long chains to said fatty acid compounds of from 25:1 to 6.5:1, more preferably from 20:1 to 10:1 and most preferably from 20:1 to 15:1. Indeed, if used outside of these ratios, the resulting product will tend to exhibit phase instability and/or viscosity problems.
  • Inorganic viscosity control agents which can also act like or augment the effect of the surfactant concentration aids, include water-soluble, ionizable salts which can also optionally be incorporated into the compositions of the present invention. Incorporation of these components to the composition must be processed at a very slow rate.
  • ionizable salts can be used.
  • suitable salts are the halides of the Group IA and IIA metals of the Periodic Table of the Elements, e.g., calcium chloride, magnesium chloride, sodium chloride, potassium bromide, and lithium chloride.
  • the ionizable salts are particularly useful during the process of mixing the ingredients to make the compositions herein, and later to obtain the desired viscosity.
  • the amount of ionizable salts used depends on the amount of active ingredients used in the compositions and can be adjusted according to the desires of the formulator. Typical levels of salts used to control the composition viscosity are from 20 to 20,000 parts per million (ppm), preferably from 20 to 11,000 ppm, by weight of the composition.
  • Alkylene polyammonium salts can be incorporated into the composition to give viscosity control in addition to or in place of the water-soluble, ionizable salts above.
  • these agents can act as scavengers, forming ion pairs with anionic detergent carried over from the main wash, in the rinse, and on the fabrics, and may improve softness performance. These agents may stabilise the viscosity over a broader range of temperature, especially at low temperatures, compared to the inorganic electrolytes.
  • Specific examples of alkylene polyammonium salts include L-lysine monohydrochloride and 1,5-diammonium 2-methyl pentane dihydrochloride.
  • Suitable liquid carriers are selected from water, organic solvents and mixtures thereof.
  • the liquid carrier employed in the instant compositions is preferably at least primarily water due to its low cost relative availability, safety, and environmental compatibility.
  • the level of water in the liquid carrier is preferably at least 50%, most preferably at least 60%, by weight of the carrier.
  • Mixtures of water and low molecular weight, e.g., ⁇ 200, organic solvent, e.g., lower alcohol such as ethanol, propanol, isopropanol or butanol are useful as the carrier liquid.
  • Low molecular weight alcohols include monohydric, dihydric (glycol, etc.) trihydric (glycerol, etc.), and higher polyhydric (polyols) alcohols.
  • the fabric softening composition can take a variety of physical forms including liquid such as aqueous or non-aqueous compositions. Such compositions may be used as a rinse added product, or as a spray or foam product. Preferably, the present composition is in a rinse added form.
  • compositions of the invention can be added directly in the rinse both to provide adequate usage concentration, e.g., at least 50 ppm and more preferably from 100 to 10,000 ppm of the liquid rinse added fabric softener compositions of the present invention.
  • a method for treating fabrics comprising contacting said fabrics in the rinse cycle with an aqueous medium containing at least 50 ppm, preferably from 100 to 10,000 ppm of the liquid fabric softening composition of the invention.
  • the fabric softening composition can conveniently be made according to well-known processes to the skilled person.
  • An exemplary disclosure is given in EP-A-0,668,902.
  • the following fabric softening composition according to the present invention was prepared: Component A DEQA 19.0 Hydrochlorid acid 0.02 Soil Release Polymer 0.2 PEG 0.6 Perfume 1.0 Electrolyte 1200ppm Dye 50ppm Sandofix TPS 5.0 Water and minors to balance to 100%

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Detergent Compositions (AREA)

Description

    Field of the invention
  • The present invention relates to fabric softening compositions and more particularly to compositions which reduce the amount of dyes released from coloured fabrics upon wet treatment such as those which occur in a laundry operation.
  • Background of the invention
  • The domestic treatment of coloured fabrics is a problem known in the art to the formulator of laundry compositions. More particularly, the problem of formulating laundry compositions which reduce the amount of dyes released from coloured fabrics upon wet treatment is a particular challenge to the formulator. This problem is now even more acute with the trends of consumer to move towards more colored fabrics.
  • Numerous solutions have been proposed in the art to solve this problem such as by treating the fabric with a dye scavenger during the washing process as described in EP 0,341,205, EP 0,033,815 and with a polyvinyl substance as described in WO 94/11482 or in the rinse cycle with a dye fixing agent as described in EP 0,462,806. However, a problem encountered with these solutions is that the dye fixing agents when used in the washing process may be destroyed or damaged by contact on storage and/or during the process, whilst when used in the rinse cycle the need for a detergent active and a high level of dye fixing agent is required to provide effective dye fixation performance. Furthermore, a problem related with the use of dye fixing agents in a softening composition is that of its weight efficiency. So that, although levels of dye fixing agents above 10% by weight would provide effective dye fixation, such use would result in an increase in the formulation cost. Another problem relating to the use of a high level of dye fixing agents in fabric softening compositions is that the resulting products show phase instability. On the other hand, lowering the level of dye fixing agents would not provide sufficient dye fixing properties and the need for a detergent material would be required.
  • Accordingly, notwithstanding the advances in the art, there is still a need for a fabric softening composition which effectively reduces the amount of dyes released from coloured fabrics upon wet treatment.
  • The Applicant has now found that the use of a liquid composition comprising a cationic fabric softener having at least two long chains, a cationic dye fixing agent in amount of 0.1% to 10% by weight, said composition being free of detergent materials, fulfills such a need.
  • It is therefore an advantage of the invention to provide liquid fabric softening compositions which provide effective reduction of the amount of dyes released from coloured fabrics upon wet domestic treatments.
  • It is another advantage of the invention to provide liquid fabric softening compositions with effective softening properties.
  • It is another advantage of the invention to provide liquid fabric softening compositions with effective storage stability properties.
  • For the purpose of the invention, the term "detergent materials" encompasses detergent surfactant materials selected from soaps, non-soap anionic, nonionic, zwitterionic and amphoteric synthetic and natural detergent surfactants which are not softeners. Not included by this definition are the fatty acids which are fabric softeners, contrary to said soaps components which do not have fabric softener properties.
  • Summary of the invention
  • The present invention relates to a liquid fabric softening composition comprising a cationic fabric softener having at least two long chains as defined in claim 1 and a cationic dye fixing agent in amount of 0.1% to 10% by weight, said composition being free of detergent materials.
  • In accordance with another aspect of the present invention, a method for treating fabrics is provided. The method comprises contacting the fabrics during the rinse cycle of a consumer laundry process with an aqueous medium containing at least 50 ppm of a fabric softening composition of the invention.
  • Detailed description of the invention Cationic fabric softeners
  • An essential component of the invention is a cationic fabric softener component having at least two long chains as defined in claim 1. By component having at least two long chains is meant a component containing at least two alkyl or alkenyl chains, each comprising from 10 to 25 carbon atoms. Such fabric softener provides effective softness benefit to the treated fabrics.
  • Typical levels of said fabric softener components within the liquid softener compositions are from 1% to 80% by weight of the compositions. Depending on the composition execution which can be dilute with a preferred level of fabric softening components from 1% to 5%, or concentrated, with a preferred level of fabric softening components from 5% to 80%, more preferably 10% to 50%, most preferably 15% to 35% by weight.
  • Typical cationic fabric softening components as defined in claim 1 having at least two long chains include the water-insoluble quaternary-ammonium fabric softening actives, the most commonly used having been di-long alkyl chains ammonium chloride.
  • In recent years, the need has arisen for more environmental-friendly materials, and rapidly biodegradable quaternary ammonium compounds have been presented as alternatives to the traditionally used di-long chain ammonium chlorides. Such quaternary ammonium compounds contain long chain alk(en)yl groups interrupted by functional groups such as carboxy groups. Said materials and fabric softening compositions containing them are disclosed in numerous publications such as EP-A-0,040,562, and EP-A-0,239,910.
  • The quaternary ammonium compounds and amine precursors herein have the formula (I) or (II), below:
    Figure 00040001
    wherein Q is selected from -O-C(O)-, -C(O)-O-, -O-C(O)-O-, -NR4-C(O)-,
    -C(O)-NR4-;
    R1 is (CH2)n-Q-T2 or T3;
    R2 is (CH2)m-Q-T4 or T5 or R3;
    R3 is C1-C4 alkyl or C1-C4 hydroxyalkyl or H;
    R4 is H or C1-C4 alkyl or C1-C4 hydroxyalkyl;
    T1, T2, T3, T4, T5 are independently C11-C22 alkyl or alkenyl;
    n and m are integers from 1 to 4; and
    X- is a softener-compatible anion.
  • Non-limiting examples of softener-compatible anions include chloride or methyl sulfate.
  • The alkyl, or alkenyl, chain T1, T2, T3, T4, T5 must contain at least 11 carbon atoms, preferably at least 16 carbon atoms. The chain may be straight or branched.
  • Tallow is a convenient and inexpensive source of long chain alkyl and alkenyl material. The compounds wherein T1, T2, T3, T4, T5 represents the mixture of long chain materials typical for tallow are particularly preferred.
  • Specific examples of quaternary ammonium compounds suitable for use in the aqueous fabric softening compositions herein include:
  • 1) N,N-di(tallowoyl-oxy-ethyl)-N,N-dimethyl ammonium chloride;
  • 2) N,N-di(tallowoyl-oxy-ethyl)-N-methyl, N-(2-hydroxyethyl) ammonium chloride;
  • 3) N,N-di(2-tallowyl-oxy-2-oxo-ethyl)-N,N-dimethyl ammonium chloride;
  • 4) N,N-di(2-tallowyl-oxy-ethylcarbonyl-oxy-ethyl)-N,N-dimethyl ammonium chloride;
  • 5) N-(2-tallowoyl-oxy-2-ethyl)-N-(2-tallowyl-oxy-2-oxo-ethyl)-N,N-dimethyl ammonium chloride;
  • 6) N,N,N-tri(tallowyl-oxy-ethyl)-N-methyl ammonium chloride;
  • 7) N-(2-tallowyl-oxy-2-oxo-ethyl)-N-(tallowyl-N,N-dimethyl-ammonium chloride;
  • 8) N - methyl - N - (3 - tallowamidopropyl) , N-(2-tallowoyloxyethyl) ammonium chloride;
  • 9) 1,2-ditallowyl-oxy-3-trimethylammoniopropane chloride;
  • and mixtures of any of the above materials.
  • Of these, compounds 1-8 are examples of compounds of Formula (I); compound 9 is a compound of Formula (II). Particularly preferred is N,N-di(tallowoyl-oxy-ethyl)-N,N-dimethyl ammonium chloride, where the tallow chains are at least partially unsaturated. The level of unsaturation of the tallow chain can be measured by the Iodine Value (IV) of the corresponding fatty acid, which in the present case should preferably be in the range of from 5 to 100 with two categories of compounds being distinguished, having a IV below or above 25. Indeed, for compounds of Formula (I) made from tallow fatty acids having an IV of from 5 to 25, preferably 15 to 20, it has been found that a cis/trans isomer weight ratio greater than 30/70, preferably greater than 50/50 and more preferably greater than 70/30 provides optimal concentrability. For compounds of Formula (I) made from tallow fatty acids having an IV of above 25, the ratio of cis to trans isomers has been found to be less critical unless very high concentrations are needed.
    Other examples of suitable quaternary ammoniums of Formula (I) and (II) are obtained by, e.g.:
    • replacing "tallow" in the above compounds with, for example, coco, palm, lauryl, oleyl, ricinoleyl, stearyl, palmityl, or the like, said fatty acyl chains being either fully saturated, or preferably at least partly unsaturated;
    • replacing "methyl" in the above compounds with ethyl, ethoxy, propyl, propoxy, isopropyl, butyl, isobutyl or t-butyl;
    • replacing "chloride" in the above compounds with bromide, methylsulfate, formate, sulfate, nitrate, and the like.
  • In fact, the anion is merely present as a counterion of the positively charged quaternary ammonium compounds. The nature of the counterion is not critical at all to the practice of the present invention. The scope of this invention is not considered limited to any particular anion.
  • By "amine precursors thereof' is meant the secondary or tertiary amines corresponding to the above quaternary ammonium compounds, said amines being substantially protonated in the present compositions due to the pH values.
  • For the preceding biodegradable fabric softening agents, the pH of the compositions herein is an essential parameter of the present invention. Indeed, it influences the stability of the quaternary ammonium or amine precursors compounds, especially in prolonged storage conditions. The pH, as defined in the present context, is measured in the neat compositions at 20°C. For optimum hydrolytic stability of these compositions, the neat pH, measured in the above-mentioned conditions, must be in the range of from 2.0 to 4.5. Preferably, where the liquid fabric softening compositions of the invention are in a diluted form, the pH of the neat composition is in the range of 2.0 to 3.0. The pH of these compositions herein can be regulated by the addition of a Bronsted acid. Examples of suitable adds include the inorganic mineral acids, carboxylic acids, in particular the low molecular weight (C1-C5) carboxylic acids, and alkylsulfonic acids. Suitable inorganic acids include HCI, H2SO4, HNO3 and H3PO4. Suitable organic acids include formic, acetic, citric, methylsulfonic and ethylsulfonic acid. Preferred acids are citric, hydrochloric, phosphoric, formic, methylsulfonic acid, and benzoic acids.
  • Cationic dye fixative agent
  • The other essential component of the invention is a cationic dye fixative agent. Cationic dye fixing agents, or "fixatives", are well-known, commercially available materials which are designed to improve the appearance of dyed fabric by minimizing the loss of dye from fabrics due to washing. Cationic dye fixatives are based on various quaternized or otherwise cationically charged organic nitrogen compounds. Cationic fixatives are available under various trade names from several suppliers. Representative examples include: CROSCOLOR PMF (July 1981, Code No. 7894) and CROSCOLOR NOFF (January 1988, Code No. 8544) from Crosfield; INDOSOL E-50 (February 27, 1984, Ref. No. 6008.35.84; polyethyleneamine-based) from Sandoz; SANDOFIX TPS, which is also available from Sandoz and is a preferred polycationic fixative for use herein and SANDOFIX SWE (cationic resinous compound), REWIN SRF, REWIN SRF-O and REWIN DWR from CHT-Beitlich GMBH.
  • Other cationic dye fixing agents are described in "Aftertreatments for improving the fastness of dyes on textile fibres" by Christopher C. Cook (REV. PROG. COLORATION Vol. 12, 1982). Dye fixing agents suitable for use in the present invention are ammonium compounds such as fatty acid - diamine condensates e.g. the hydrochloride, acetate, metosulphate and benzyl hydrochloride of oleyldiethyl aminoethylamide, oleylmethyl-diethylenediaminemethosulphate, monostearyl-ethylene diaminotrimethylammonium methosulphate and oxidized products of tertiary amines; derivatives of polymeric alkyldiamines, polyamine-cyanuric chloride condensates and aminated glycerol dichlorohydrins.
  • The amount of dye fixing agent to be employed in the composition of the invention is in amount of from 0.1% to 10% by weight of the composition, preferably from 0.5% to 8% by weight, more preferably from 0.8% to 5.5% by weight of the composition.
  • For optimum dye fixing benefit as well as softness benefit, the weight ratio of fabric softener to dye fixing agent is of from 60:1 to 1.5:1, more preferably from 20:1 to 3.5:1, most preferably from 10:1 to 3.5:1.
  • Detergent materials
  • For the purpose of the invention, the term "detergent materials" encompasses detergent surfactant materials selected from soaps, non-soap anionic, nonionic, zwitterionic and amphoteric synthetic and natural detergent surfactants which are not softeners. Not included by this definition are the fatty acids which are fabric softeners, contrary to said soaps components which do not have fabric softener properties.
  • Soaps and non-soaps anionic materials are the linear and branched primary alkyl sulfates, alkyl ethoxysulfates, fatty oleyl glycerol sulfates, alkyl phenol ethylene oxide ether sulfates, the C5-C17 acyl-N-(C1-C4 alkyl) and -N-(C1-C2 hydroxyalkyl) glucamine sulfates, and sulfates of alkylpolysaccharides; anionic sulfonate surfactants such as the salts of C5-C20 linear alkylbenzene sulfonates, alkyl ester sulfonates, C6-C22 primary or secondary alkane sulfonates, C6-C24 olefin sulfonates, sulfonated polycarboxylic acids, alkyl glycerol sulfonates, fatty acyl or oleyl glycerol sulfonates, alkyl ethoxy carboxylates, and the alkali metal sarcosinates.
  • Nonionic detergent materials are the polyhydroxy fatty acid amides, polyethylene, polypropylene, and polybutylene oxide condensates of alkyl phenols; alkyl ethoxylate condensation products of aliphatic alcohols with from about 1 to about 25 moles of ethylene oxide; ethoxylated C6-C18 fatty alcohols and C6-C18 mixed ethoxylated/propoxylated fatty alcohols; alkylpolysaccharides and the fatty acid amides.
  • Zwiterrionic and amphoteric materials are the amine oxides, the alkyl amphocarboxylic acids, the betaines such as coconut acylamidopropyldimethyl betaine and hexadecyl dimethyl betaine.
  • Additional components
  • The composition may also optionally contain additional components such as additional fabric softener materials, electrolyte concentration aids, stabilisers, such as well known antioxidants and reductive agents, soil release polymers, bacteriocides, colorants, perfumes, preservatives, optical brighteners, anti ionisation agents, antifoam agents and chelating agents.
  • Additional fabric softener materials
  • Additional fabric softening materials may be used in addition to the di-long chain cationic fabric softener. When used, such additional fabric softening materials will typically be present in an amount of from 0 to 15% by weight of the composition. Such materials are the single long chain alkyl cationic softeners and/or the fatty acids.
  • Single long chain alkyl cationic softeners
  • Such mono-long-chain-alkyl cationic softeners suitable for use herein are, preferably, quaternary ammonium salts of the general formula [R2N+R3] X- wherein the R2 group is C10-C22 hydrocarbon group, preferably C12-C18 alkyl group of the corresponding ester linkage interrupted group with a short alkylene (C1-C4) group between the ester linkage and the N, and having a similar hydrocarbon group, e.g., a fatty acid ester of choline, preferably C12-C14 (coco) choline ester and/or C16-C18 tallow choline ester at from 0.1% to 20% by weight of the softener active. Each R3 is a C1-C4 alkyl or substituted (e.g., hydroxy) alkyl, or hydrogen, preferably methyl, and the counterion X- is a softener compatible anion, for example, chloride, bromide, methyl sulfate, etc. Other cationic materials with ring structures such as alkyl imidazoline, imidazolinium, pyridine, and pyridinium salts having a single C12-C30 alkyl chain can also be used. Very low pH is required to stabilize, e.g., imidazoline ring structures.
  • Some alkyl imidazolinium salts and their imidazoline precursors useful in the present invention have the general formula :
    Figure 00100001
    wherein Y2 is -C(O)-O-, -O-(O)C-, -C(O)-N(R5)-, or -N(R5)-C(O)- in which R5 is hydrogen or a C1-C4 alkyl radical; R6 is a C1-C4 alkyl radical or H (for imidazoline precursors); R7 and R8 are each independently selected from R3 and R2 as defined hereinbefore for the single-long-chain cationic surfactant with only one being R2.
  • Some alkyl pyridinium salts useful in the present invention have the general formula:
    Figure 00100002
    wherein R2 and X- are as defined above. A typical material of this type is cetyl pyridinium chloride.
  • Fatty acids
  • Suitable fatty acids include those containing from 10 to 25, preferably from 12 to 25 total carbon atoms, with the fatty moiety containing from 10 to 22, preferably from 16 to 22, carbon atoms. The shorter moiety contains from 1 to 4, preferably from 1 to 2 carbon atoms. The level of unsaturation of the tallow chain can be measured by the Iodine Value (IV) of the corresponding fatty acid, which in the present case should preferably be in the range of from 5 to 100, more preferably in the range of from 0 to 25.
  • Specific examples of fatty acid compounds suitable for use in the liquid fabric softening compositions herein include compounds selected from lauric acid, myristic acid, palmitic acid, stearic acid, arachidic acid, behenic acid, oleic acid, coconut fatty acid, tallow fatty acid, partially hydrogenated tallow fatty acid and mixtures thereof. A most preferred fatty acid compound is tallow fatty acid with an Iodine Value (IV) of 18.
  • When the above mentioned fatty acids are used, the fatty acid will be present in a weight ratio of said cationic fabric softening agents having di-long chains to said fatty acid compounds of from 25:1 to 6.5:1, more preferably from 20:1 to 10:1 and most preferably from 20:1 to 15:1. Indeed, if used outside of these ratios, the resulting product will tend to exhibit phase instability and/or viscosity problems.
  • Electrolyte Concentration Aids
  • Inorganic viscosity control agents which can also act like or augment the effect of the surfactant concentration aids, include water-soluble, ionizable salts which can also optionally be incorporated into the compositions of the present invention. Incorporation of these components to the composition must be processed at a very slow rate.
  • A wide variety of ionizable salts can be used. Examples of suitable salts are the halides of the Group IA and IIA metals of the Periodic Table of the Elements, e.g., calcium chloride, magnesium chloride, sodium chloride, potassium bromide, and lithium chloride. The ionizable salts are particularly useful during the process of mixing the ingredients to make the compositions herein, and later to obtain the desired viscosity. The amount of ionizable salts used depends on the amount of active ingredients used in the compositions and can be adjusted according to the desires of the formulator. Typical levels of salts used to control the composition viscosity are from 20 to 20,000 parts per million (ppm), preferably from 20 to 11,000 ppm, by weight of the composition.
  • Alkylene polyammonium salts can be incorporated into the composition to give viscosity control in addition to or in place of the water-soluble, ionizable salts above. In addition, these agents can act as scavengers, forming ion pairs with anionic detergent carried over from the main wash, in the rinse, and on the fabrics, and may improve softness performance. These agents may stabilise the viscosity over a broader range of temperature, especially at low temperatures, compared to the inorganic electrolytes. Specific examples of alkylene polyammonium salts include L-lysine monohydrochloride and 1,5-diammonium 2-methyl pentane dihydrochloride.
  • Another ingredient is a liquid carrier. Suitable liquid carriers are selected from water, organic solvents and mixtures thereof. The liquid carrier employed in the instant compositions is preferably at least primarily water due to its low cost relative availability, safety, and environmental compatibility. The level of water in the liquid carrier is preferably at least 50%, most preferably at least 60%, by weight of the carrier. Mixtures of water and low molecular weight, e.g., <200, organic solvent, e.g., lower alcohol such as ethanol, propanol, isopropanol or butanol are useful as the carrier liquid. Low molecular weight alcohols include monohydric, dihydric (glycol, etc.) trihydric (glycerol, etc.), and higher polyhydric (polyols) alcohols.
  • Form of the composition
  • The fabric softening composition can take a variety of physical forms including liquid such as aqueous or non-aqueous compositions.
    Such compositions may be used as a rinse added product, or as a spray or foam product. Preferably, the present composition is in a rinse added form.
  • The compositions of the invention can be added directly in the rinse both to provide adequate usage concentration, e.g., at least 50 ppm and more preferably from 100 to 10,000 ppm of the liquid rinse added fabric softener compositions of the present invention.
  • Accordingly, a method is provided for treating fabrics comprising contacting said fabrics in the rinse cycle with an aqueous medium containing at least 50 ppm, preferably from 100 to 10,000 ppm of the liquid fabric softening composition of the invention.
  • Process
  • The fabric softening composition can conveniently be made according to well-known processes to the skilled person. An exemplary disclosure is given in EP-A-0,668,902.
  • The invention is illustrated in the following non-limiting examples, in which all percentages are on a weight basis unless otherwise stated.
  • In the examples, the abbreviated component identifications have the following meanings:
  • DEQA :
    Di-(tallowoyl-oxy-ethyl) dimethyl ammonium chloride
    Fatty acid :
    Stearic acid of IV=18
    Electrolyte :
    Calcium chloride
    PEG :
    Polyethylene Glycol MW 4000
    Example 1
  • The following fabric softening composition according to the present invention was prepared:
    Component A
    DEQA 19.0
    Hydrochlorid acid 0.02
    Soil Release Polymer 0.2
    PEG 0.6
    Perfume 1.0
    Electrolyte 1200ppm
    Dye 50ppm
    Sandofix TPS 5.0
    Water and minors to balance to 100%
  • Example 2
  • The following fabric softening compositions are in accordance with the invention:
    Component B C D
    DEQA 2.6 2.9 18.0
    Fatty acid 0.3 - 1.0
    Hydrochlorid acid 0.02 0.02 0.02
    Soil Release Polymer - - 0.2
    PEG - - 0.6
    Perfume 1.0 0.5 1.0
    Electrolyte - - 600ppm
    Dye 10ppm 10ppm 50ppm
    Sandofix TPS 1.6 1.6 5.0
    Water and minors to balance to 100%

Claims (6)

  1. A liquid fabric softening composition comprising a cationic fabric softener having at least two long chains and a cationic dye fixing agent in amount of 0.1% to 10% by weight, said composition being free of detergent materials, wherein each of said chains comprises an alkyl or alkenyl chain having from 10 to 25 carbon atoms and wherein said fabric softener is a biodegradable fabric softening material.
  2. A liquid fabric softening composition according to Claim 1, wherein said cationic dye fixing agent is a polycationic dye fixing agent.
  3. A liquid fabric softening composition according to either one of Claims 1 or 2, wherein said cationic dye fixing agent is in amount of from 0.5% to 8% by weight, preferably from 0.8% to 5.5% by weight of the composition.
  4. A liquid fabric softening composition according to Claim 1 wherein said biodegradable fabric softening material is selected from quaternary ammonium compounds and amine precursors having the formula (I) or (II), below:
    Figure 00150001
    wherein Q is selected from -O-C(O)-, -C(O)-O-, -O-C(O)-O-, -NR4-C(O)-, -C(O)-NR4-;
    R1 is (CH2)n-Q-T2 or T3;
    R2 is (CH2)m-Q-T4 or T5 or R3;
    R3 is C1-C4 alkyl or C1-C4 hydroxyalkyl or H;
    R4 is H or C1-C4 alkyl or C1-C4 hydroxyalkyl;
    T1, T2, T3, T4, T5 are independently C11-C22 alkyl or alkenyl;
    n and m are integers from 1 to 4; and
    X- is a softener-compatible anion.
  5. A liquid fabric softening composition according to any one of Claims 1-4 wherein said fabric softener is present in amount of 1% to 80% by weight.
  6. A method for treating fabrics comprising contacting said fabrics in the rinse cycle with an aqueous medium containing at least 50 ppm of a liquid fabric softening composition according to any one of Claims 1-5.
EP96870068A 1996-06-03 1996-06-03 Fabric softening compositions Expired - Lifetime EP0811679B1 (en)

Priority Applications (11)

Application Number Priority Date Filing Date Title
EP96870068A EP0811679B1 (en) 1996-06-03 1996-06-03 Fabric softening compositions
DE69628285T DE69628285T2 (en) 1996-06-03 1996-06-03 Fabric softener compositions
ES96870068T ES2200047T3 (en) 1996-06-03 1996-06-03 SOFTENING COMPOSITIONS OF FABRICS.
CN97197016A CN1093878C (en) 1996-06-03 1997-05-23 Fabric softening compositions
CZ983945A CZ394598A3 (en) 1996-06-03 1997-05-23 Preparations for softening fabrics
CA002257201A CA2257201A1 (en) 1996-06-03 1997-05-23 Fabric softening compositions
AU32874/97A AU3287497A (en) 1996-06-03 1997-05-23 Fabric softening compositions
BR9709634A BR9709634A (en) 1996-06-03 1997-05-23 Fabric softening compositions
PCT/US1997/008966 WO1997046651A1 (en) 1996-06-03 1997-05-23 Fabric softening compositions
JP50065098A JP3784417B2 (en) 1996-06-03 1997-05-23 Fabric softening composition
ARP970102382A AR007374A1 (en) 1996-06-03 1997-06-02 LIQUID COMPOSITIONS SOFTENING OF FABRICS AND METHOD OF TREATMENT USING THE SAME

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP96870068A EP0811679B1 (en) 1996-06-03 1996-06-03 Fabric softening compositions

Publications (2)

Publication Number Publication Date
EP0811679A1 EP0811679A1 (en) 1997-12-10
EP0811679B1 true EP0811679B1 (en) 2003-05-21

Family

ID=8226145

Family Applications (1)

Application Number Title Priority Date Filing Date
EP96870068A Expired - Lifetime EP0811679B1 (en) 1996-06-03 1996-06-03 Fabric softening compositions

Country Status (11)

Country Link
EP (1) EP0811679B1 (en)
JP (1) JP3784417B2 (en)
CN (1) CN1093878C (en)
AR (1) AR007374A1 (en)
AU (1) AU3287497A (en)
BR (1) BR9709634A (en)
CA (1) CA2257201A1 (en)
CZ (1) CZ394598A3 (en)
DE (1) DE69628285T2 (en)
ES (1) ES2200047T3 (en)
WO (1) WO1997046651A1 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0990695A1 (en) 1998-09-30 2000-04-05 Witco Surfactants GmbH Fabric softener with dye transfer inhibiting properties
BR9915536A (en) * 1998-10-23 2001-10-16 Procter & Gamble Composition and method for tissue care
DE10150724A1 (en) 2001-03-03 2003-04-17 Clariant Gmbh Washing agents such as detergents contain dye transfer inhibitors which are polyamine/cyanamide/amidosulfuric acid, cyanamide/aldehyde/ammonium salt or amine/epichlorhydrin reaction products
EP1239025A3 (en) 2001-03-03 2003-09-03 Clariant GmbH Detergent composition and laundry treatment compositon comprising dye transfer inhibiting and dye fixing agent
CN102844422B (en) 2010-04-22 2016-01-20 荷兰联合利华有限公司 Relate to the improvement of fabric conditioner

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3501521A1 (en) * 1985-01-18 1986-07-24 Henkel KGaA, 4000 Düsseldorf AQUEOUS CONCENTRATED TEXTILE SOFTENER
JPH03199472A (en) * 1989-12-27 1991-08-30 Kao Corp Liquid softening, finishing agent
JPH0441776A (en) * 1990-06-01 1992-02-12 Kao Corp Liquid soft finishing agent
GB9013784D0 (en) * 1990-06-20 1990-08-08 Unilever Plc Process and composition for treating fabrics
GB9301728D0 (en) * 1993-01-28 1993-03-17 Unilever Plc Fabric softening composition
US5616553A (en) * 1993-08-12 1997-04-01 The Procter & Gamble Company Fabric conditioning compositions
US5445747A (en) * 1994-08-05 1995-08-29 The Procter & Gamble Company Cellulase fabric-conditioning compositions

Also Published As

Publication number Publication date
AR007374A1 (en) 1999-10-27
EP0811679A1 (en) 1997-12-10
CN1227594A (en) 1999-09-01
DE69628285T2 (en) 2004-04-01
BR9709634A (en) 1999-08-10
CN1093878C (en) 2002-11-06
CZ394598A3 (en) 1999-07-14
WO1997046651A1 (en) 1997-12-11
DE69628285D1 (en) 2003-06-26
JP2000503733A (en) 2000-03-28
ES2200047T3 (en) 2004-03-01
JP3784417B2 (en) 2006-06-14
CA2257201A1 (en) 1997-12-11
AU3287497A (en) 1998-01-05

Similar Documents

Publication Publication Date Title
CA2250909C (en) Fabric softener compositions
US6316402B1 (en) Fabric softening compositions
JPH09509455A (en) Cellulase fabric conditioning composition
CA2250225A1 (en) Use of a fabric softener composition
CA2168874C (en) Fabric-conditioning compositions
AU765389B2 (en) Rinse-added fabric care compositions comprising low molecular weight linear and cyclic polyamines
EP0811679B1 (en) Fabric softening compositions
US6143712A (en) Fabric softening compositions
CA2257199C (en) Fabric softening compositions
CA2232413C (en) Stabilised fabric softening compositions
US5929025A (en) Stabilized fabric softening compositions comprising a fabric softening compound, fatty acid, and perfume
EP0754749A1 (en) Fabric softeners containing water soluble dyes for reduced staining
MXPA98010164A (en) Softener compositions of te
CA2391904A1 (en) Method for providing in-wear comfort
EP0891408A1 (en) Use of a fabric softener composition
MXPA98007977A (en) The use of a te 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: A1

Designated state(s): AT BE CH DE DK ES FI FR GB GR IE IT LI LU NL PT SE

17P Request for examination filed

Effective date: 19980512

17Q First examination report despatched

Effective date: 20011126

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

RBV Designated contracting states (corrected)

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

AK Designated contracting states

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

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REF Corresponds to:

Ref document number: 69628285

Country of ref document: DE

Date of ref document: 20030626

Kind code of ref document: P

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2200047

Country of ref document: ES

Kind code of ref document: T3

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

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

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

ET Fr: translation filed
REG Reference to a national code

Ref country code: IE

Ref legal event code: MM4A

26N No opposition filed

Effective date: 20040224

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

Ref country code: ES

Payment date: 20100618

Year of fee payment: 15

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

Ref country code: IT

Payment date: 20100621

Year of fee payment: 15

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

Ref country code: NL

Payment date: 20100607

Year of fee payment: 15

REG Reference to a national code

Ref country code: NL

Ref legal event code: V1

Effective date: 20120101

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

Ref country code: IT

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

Effective date: 20110603

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: 20120101

REG Reference to a national code

Ref country code: ES

Ref legal event code: FD2A

Effective date: 20120717

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 NON-PAYMENT OF DUE FEES

Effective date: 20110604

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

Ref country code: FR

Payment date: 20120614

Year of fee payment: 17

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

Effective date: 20140228

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

Ref country code: FR

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

Effective date: 20130701

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

Ref country code: GB

Payment date: 20150526

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: 20150630

Year of fee payment: 20

REG Reference to a national code

Ref country code: DE

Ref legal event code: R071

Ref document number: 69628285

Country of ref document: DE

REG Reference to a national code

Ref country code: GB

Ref legal event code: PE20

Expiry date: 20160602

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: 20160602