EP0086104A2 - Method of softening fabrics - Google Patents

Method of softening fabrics Download PDF

Info

Publication number
EP0086104A2
EP0086104A2 EP83300624A EP83300624A EP0086104A2 EP 0086104 A2 EP0086104 A2 EP 0086104A2 EP 83300624 A EP83300624 A EP 83300624A EP 83300624 A EP83300624 A EP 83300624A EP 0086104 A2 EP0086104 A2 EP 0086104A2
Authority
EP
European Patent Office
Prior art keywords
lanolin
liquor
cationic
fabric softening
fabric
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
EP83300624A
Other languages
German (de)
French (fr)
Other versions
EP0086104A3 (en
EP0086104B1 (en
Inventor
Michael William Parslow
Edwin Willis
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 NV
Original Assignee
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=10528227&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP0086104(A2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Unilever NV filed Critical Unilever NV
Priority to AT83300624T priority Critical patent/ATE42762T1/en
Publication of EP0086104A2 publication Critical patent/EP0086104A2/en
Publication of EP0086104A3 publication Critical patent/EP0086104A3/en
Application granted granted Critical
Publication of EP0086104B1 publication Critical patent/EP0086104B1/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/001Softening compositions
    • C11D3/0015Softening compositions liquid
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/62Quaternary ammonium compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2093Esters; Carbonates

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Treatment Of Fiber Materials (AREA)
  • Prostheses (AREA)
  • Electrical Discharge Machining, Electrochemical Machining, And Combined Machining (AREA)
  • Materials For Medical Uses (AREA)

Abstract

A method of treating fabrics comprises contacting the fabrics with an aqueous liquor having a pH less than about 7.5, such as between about 5.0 and about 7.0, the liquor containing a cationic fabric softener and lanolin The liquor is formed by adding to water a composition containing the cationic fabric softener and the lanolin, the concentration of these components in the liquor preferably being from 50 ppm to 500 ppm. The lanolin may be replaced by a lanolin-like material such as derivatives thereof or one or more of the active constituents of lanolin either extracted therefrom or derived from other sources. Preferred ratios of cationic softener to lanolin are 20:1 to 1:20 by weight. A liquor to flabric ratio of less than 25:1 is preferred. The method generally leads to a deposition of cationic softener and lanolin of less than 0.5% by weight of the fabric.

Description

    FIELD OF THE INVENTION
  • The present invention relates to a fabric softening composition and a method for its use.. In particular, but not exclusively, it relates to an aqueous based concentrated fabric softening composition.
  • BACKGROUND ART
  • It is known to treat fabrics, particularly after washing, with fabric softening agents in order to improve the feel of the fabrics and, in the case of clothes, to improve the comfort in wear. Traditionally, fabric softening agents are applied from an aqueous liquor which is made up by adding a relatively small volume of a fabric softening composition to a large volume of water, for example during the rinse cycle in an automatic washing machine. The fabric softening composition is usually an aqueous liquid product containing less than about 8% of a cationic fabric softening agent. For a number of reasons, including for example the cost of packaging, it would be preferred if the product were to contain more than 8% of the active ingredient but due to difficulties in manufacture, storage and ease of use of the products, it has only been possible to do this in the past with some difficulty.
  • Further, there may be a desire to partially replace the cationic fabric softening agent with a material which is less costly, easier to handle or less prone to causing skin reaction while at the same time maintaining or substantially maintaining the performance of the product.
  • As set out in more detail below, the present invention seeks to overcome one or more of the objectives referred to above by the combined use of a cationic fabric softening agent and lanolin or a lanolin-like material.
  • SUMMRY OF THE INVENTION
  • According to the invention, there is provided a method of treating fabrics comprising contacting the fabrics with an aqueous liquor having a pH less than 7.5 and containing a cationic fabric softening agent, characterised in that said liquor also contains lanolin or a lanolin-like material and is formed by adding to water a liquid or granular fabric softening composition comprising a cationic fabric softening agent and lanolin or a lanolin-like material.
  • The fabric softening composition used to form the aqueous liquor may be in the form of a granular solid, a paste, a dilute liquid (containing less than about 8% by weight total cationic fabric softening agent and lanolin or lanolin-like material) or a concentrated liquid (containing more than a total of about 8% of these materials). The preferred form of the composition is an aqueous based liquid, particularly a concentrated liquid.
  • An essential component of the present invention is lanolin or a lanolin-like material. Lanolin is wool wax which has been purified by various purification steps including washing, neutralisation, filtration, bleaching and deodorisation. Lanolin is composed primarily of esters which constitute the active constituents in the present invention and which yield on hydrolysis a mixture of complex alcohols and fatty acids. The alcohols which form about half of the ester component by weight, include sterols and terpene alcohols. The sterols amount to about 30% and include cholesterol, 7-dehydrocholesterol and cerebosterol and dihydrocholesterol (cholestanol). The terpene alcohols include lanesterol (C30H50O), dihydrolanesterol (C30HS20), agnosterol (C30H48O), dihydroagnosterol (C30H50).
  • Lanolin is available commercially in a number of forms. Lanolin as such contains the active constituents primarily in their ester form. It is also available in two hydrolysed forms where the active constituents are primarily in their alcoholic or carboxylic acid form. Further, lanolin may be hydrogenated to form a product where the active constituents are present primarily only in their alcoholic form. Lanolin is also commercially available in propoxylated and acetylated forms. As used herein the term "lanolin" is intended to refer to any such material derived from wool wax whether the active constituents are in the alcoholic, ester, alkoxylated, hydrogenated or other chemical form.
  • Suitable commercial forms of lanolin include Corona (lanolin BP), Hartolan, Polychol (Trade Marks of Croda Chemicals Ltd), Solulan, Acetulan and Modulan (Trade Marks of American Cholesterol Products Inc) and Lanocerina (Trade Mark - Esperis SpA Milan), Coronet (Trade Mark - Croda Chemicals Limited). Commercial lanolin is also available from Westbrook Lanolin Co., Bradford, England.
  • Many of the active constituents of lanolin can be prepared synthetically, from sources other than wool wax, or can be extracted from wool wax and other naturally occurring materials. While for cost reasons the commercially available forms of lanolin are preferred for the present invention, it is also possible to use any one or more of the active constituents referred to above however derived, and also materials of similar structure. Thus, in place of lanolin one may use a "lanolin-like material" which term as used herein includes
    • (a) any one or more of the active lanolin constituents referred to above, and the carboxylic acid or alcohol derivatives thereof:
    • (b) the corresponding carboxylic acids or alcohols and ester derivatives of the materials listed in (a) in particular the esters thereof with fatty acids or alcohols containing at least 12 carbon atoms. 4
    • (c) iso- and anteiso alcohols and acids and derivatives thereof having the general formula
      Figure imgb0001
      where R is a divalent straight or branched chain, saturated or unsaturated, substituted or unsubstituted hydrocarbyl group having at least 7 preferably at least 15 carbon atoms, R2 is a methyl or ethyl group and X is -OH, ―COOH,
      Figure imgb0002
      or -COOR3 where R3 is a hydrocarbyl group, in particular a fatty acid alkyl group containing at least 12 carbon atoms. Examples of materials in this group include 16-methylheptadecanol, 24-methyl hexacosanol, 8-methylnonanoic acid, and 2-hydroxy-16-methylheptadecanoic acid.
  • The level of lanolin or lanolin-like material in the aqueous fabric softening compositions is preferably from about 0.25% to about 40% by weight, such as between about 1.5% and about 20% by weight of the composition.
  • Any well-known cationic fabric softening agent can be used in the present invention, as well as mixtures of two or more of such agents.
  • Suitable examples of cationic fabric-softening agents are quaternary ammonium compounds containing two long alkyl or alkenyl chains with 12-22 carbon atoms such as di(hardened or unhardened tallow) dimethyl ammoniumchloride, 2-heptadecyl-2methylstearoyl amido ethyl imidazoline methosulphate, di-(coco)dimethyl ammoniumchloride, etc. These cationic fabric-softening agents are well-known in the art and further suitable examples can be found in Schwartz-Perry: "Surface-active Agents and Detergents" Vol II, 1958.
  • Relatively water-soluble cationic softening agents, such as the monoalkyl quaternary ammonium compounds such as stearyltrimethylammoniumchloride, may also be used, but, as they are often less effective softeners, they are preferably used in conjunction with other, more effective cationic softening agents or with non-cationic softening agents such as fatty acid esters of polyols such as sorbitantristearate, glycerolmonostearate, and so on, or with anionic detergents with which they are capable of forming softening complexes, such as fatty acid soaps. They may also be made more hydrophobic by treatment with suitable hydrophobising agents such as long chain alcohols and fatty acids. The present invention is however of particular benefit if the more effective, less water-soluble cationic softening agents having two long alkyl chains are used.
  • The level of cationic fabric softening agent in the aqueous fabric softening compositions is preferably from 0.5% to 30% by weight, such as between 1.0% and 15% by weight of the composition.
  • The ratio by weight of the cationic fabric softening agent to the lanolin or lanolin-like material may lie between 0.05:1 and 20:1, more preferably between 0.1:1 and 10:1, especially between 1:1 and 4:1.
  • In use, the fabric softening composition of the invention is added to a large volume of water to form a liquor with which the fabrics to be treated are contacted. Generally, the total concentration of the cationic fabric softening agent and the lanolin or lanolin-like materials in this liquor will be between 50 ppm and 500 ppm.
  • The pH of the liquor should be less than 7.5, and is preferably between 5.0 and 7.0.
  • The pH of the aqueous composition used for forming the liquor may be varied within a somewhat wider range, for example between 3 and 8, preferably from 4 to 6. To achieve the desired pH in the composition and in the treatment liquor, the composition may contain buffering agents as required, such as benzoic acid, citric acid and phosphoric acids and/or their alkali metal salts.
  • In use, the fabrics to be treated are contacted with an aqueous liquor to which the fabric softening composition is added, the ratio by weight of the fabrics to the liquor being preferably less than 25:1, most preferably between 10:1 and 4:1.
  • The aqueous liquor in contact with the fabrics may be at any convenient temperature. Successful results can be obtained when the liquor has a temperature between about 0°C and about 60°C, preferably between about 10°C and about 40°C.
  • The liquor and fabrics in contact therewith are preferably agitated during treatment.
  • The amount of cationic softening agent and lanolin or lanolin-like material deposited on the fabric depends on, inter alia, the concentration of these components in the treatment liquor, the treatment temperature, the degree of agitation, the treatment time and the nature of the fabric. Generally, a level of less than 0.5%, such as between 0.01% and 0.4% by weight in total of these components will be deposited, based on the weight of the dry fabric.
  • The balance of the composition generally comprises the aqueous medium, optionally with the other ingredients as set out below. The aqueous medium comprises at least 25%, preferably at least 30%, and especially at least 40% of the composition.
  • The compositions of the invention may further comprise additional beneficial ingredients, commonly used or proposed for inclusion in fabric-softening compositions. Such ingredients, either alone or incorporated in suitable carriers, include viscosity modifiers, germicides, fluorescers, perfumes including deodorising perfumes, organic or inorganic acids, antistatic agents such as water-soluble cationic surfactants, ethoxylated quaternary polyamine compounds (eg Ethoduameen T 13) and aluminium salts, soil-release agents, colourants, antioxidants, bleaches, bleach precursors, anti-yellowing agents, ironing aids etc, all in the conventional minor amounts. Enzymes such as cellulases may also be included.
  • The compositions may also contain, in addition to the cationic fabric-softening agents, other non-cationic fabric-softening agents such as nonionic fabric-softening agents.
  • In particular, when in liquid form, the'compositions may include viscosity modifiers such as polymers as described below, C12-C40 hydrocarbons, C9-C24 fatty acids, fatty acid esters having a total of 10-40 carbon atoms, C10-C18 fatty alcohols, electrolytes, and water-miscible solvents.
  • The polymer when included in the composition of the invention may be present therein in an amount of from 0.5 to 40%, preferably from 1 to 30%, and particularly preferably 4-25%. The polymer, suitable for inclusion, is defined in the following way:
    • The polymer should be water-soluble under user's conditions, and a 20% aqueous solution of the polymer
    should have viscosity (η) of < 50, preferably < 30 and especially preferably < 15 cP, as measured at 25°C and 110 sec-1 in a Haake Viscometer. Said 20% aqueous solution should also show a vapour pressure equal to or lower than the vapour pressure of a 2% aqueous solution of polyethyleneglycol with a molecular weight of 6,000, preferably equal to or lower than that of a 10% aqueous solution of said polyethyleneglycol, and particulary preferably equal to or lower than that of an 18% aqueous solution of said polyethyleneglycol. The said aqueous polymer solution can be of water and polymer only, or can include solvent- containing media normally derived from the raw materials or additives, or include additives specifically designed to improve the vapour pressure lowering capacity of the polymer, or, in the case of ionic polymers, include adjustments to pH in order to optimise ionisation. Such vapour pressure measurements can be obtained using an Hewlett Packard vapour pressure osmometer, using an operating temperature of 34.5°C or using any other suitable vapour measuring device.
  • The polymer should furthermore have a molecular weight of at least 400, preferably at least 4,000 and particularly preferably.at least 6,000.
  • It is desirable, furthermore, that the polymer does not negatively interact with any of the other ingredients of the composition.
  • Suitable examples of the polymer can be thus obtained from the polyalkylaeneglycols, the polyalkylene imines, dextran, gelatin and other natural or synthetic (co)polymers, as long as they meet the above criteria.
  • Mixtures of two or more polymers of the same type or of different type may also be used.
  • A preferred class of polymers comprises polyethyleneglycols with an average molecular weight of 1,000 to 6,000. These polymers, and especially those with an average molecular weight of 4,000 or 6,000, are particularly suitable for compositions of the invention with a high level of relatively water-insoluble cationic fabric-softening agent.
  • Other typical examples of suitable polymers are dextran with a molecular weight of 10,000 and polyethylene imine with a molecular weight of 45-750.
  • When the composition contains a C12-C40 hydrocarbon as a viscosity control agent, this is advantageously at a level of from 0.25% to 50% by weight, preferably from 0.5% to 25%. Preferred materials have from 12 to 24 carbon atoms and especially preferred are liquid mixtures of paraffins having from 14 to 18 carbon atoms.
  • Normally, suitable hydrocarbons are found in the paraffin and olefin series, but other materials, such as alkynes and cyclic hydrocarbons are not excluded. Materials known generally as paraffin oil, and petroleum are suitable. Examples of specific materials are hexadecane, octadecane, eicosane tetradecane and octadecane. Preferred commercially-available paraffin mixtures include spindle oil and light oil and technical grade mixtures of C14-C18 n-paraffins. Haloparaffins such as myristyl chloride and stearyl bromide are not excluded.
  • When the composition contains a C9-C24 fatty acid, this is advantageously at a level of from 0.5 to 15%.
  • Highly preferred materials of this class are the C10-C20 saturated fatty acids, especially lauric acid, myristic acid, palmitic acid and stearic acid.
  • When the composition contains a fatty acid ester having a total of 10 to 40 carbon atoms this is at a preferred level of from 0.25 to 15% by weight, advantageously 0.5 to 4%. The ester is preferably empirically derived from a fatty acid having 8 to 23 carbon atoms and an alkanol or hydroxy alkanol having 1-8, especially 1-4 carbon atoms. Specific examples include esters derived from C1-C3 alcohols and lauric, myristic, palmitic or stearic acid, such as methyl laurate, ethyl myristate, iso-propyl stearate, ethylene glycol monostearate, ethyl stearate, methyl palmitate and other esters such as iso-butyl stearate, 2-ethylhexyllaurate, iso-octyl myristate .
  • When the composition contains a fatty alcohol having from 10 to 18 carbon atoms, this is preferably at a level of from 0.25 to 15% by weight.
  • Specific examples of this class are decanol, dodecanol, tetradecanol, pentadecanol, hexadecanol and octadecanol. The most preferred materials are lauryl and palmityl alcohols.
  • When the compositions contains as viscosity control agent a solvent, this may be a lower alkanol, a glycol, a glycolether and the like. The solvent may be present at a level of up to 20% by weight, such as from 5% to 15% by weight. When the cationic fabric-softening agent is supplied in the form of an aqueous-alcoholic solution, that alcohol content is included in the above amounts, and if necessary only a small amount of extra alcohol is to be added. A suitable solvent is isopropanol.
  • The viscosity of the fabric softening composition may be controlled by the presence of an electrolyte. Preferably the electrolyte is a water-soluble non-surface active salt such as sodium chloride, sodium methosulphate, sodium benzoate calcium chloride, magnesium chloride or aluminium chlorhydrate. The level of electrolyte will determine or be determined by the desired viscosity of the composition and the nature and concentration of other components in the composition. Typical levels are from 100 to 1000 parts per million, most preferably between 200 and 500 parts per million.
  • The fabric softening compositions optionally contain one or more non ionic emulsifying agents, such as the polymerised monoglycerides of long chain fatty acids having from 14 to 24 carbon atoms in the straight or branched saturated or uasaturated carbon chain, such as poly-monolauryl glyceride, poly-monostearyl glyceride, poly-monopalmityl glyceride or poly-monooleyl glyceride. Another suitable nonionic emulsifying agent is sorbitan monostearate.
  • These nonionic emulsifying agents are available commercially by the Trade Marks WITCONOL (Witco Chemicals Ltd) and SPAN (Atlas Chemical). The nonionic emulsifying agent may be present at a level from 0.5% to 9.5% by weight, such as from 2.4% to 6%.
  • In addition to the above-discussed components, compositions according to the invention can also include a water-soluble cationic or nonionic surfactant.
  • By water-soluble, it is meant that the surfactant has a solubility in water of pH 2.5 and 20°C of greater than 10 g/1. Normally such materials are alkyl substituted ammonium salts having one C12-C24 alkyl chain, optionally substituted or interrupted by functional groups such as ―O―,―COO―,―CONH―,―O― etc. Suitable water soluble nonionic surfactants are the ethoxylated sorbitan esters available as TWEENS (Atlas Chemical).
  • It is particularly beneficial to include a water-soluble cationic or nonionic emulsifying agent in the composition if it contains as a viscosity modifier a hydrocarbon, fatty acid, fatty alcohol or fatty acid ester of the types referred to above. The level of the water-soluble surfactant is preferably 0.1% to 1%.
  • Preferably, the compositions contain substantially no anionic material such as anionic surfactants. However, some anionic material can be tolerated in practice. In preferred compositions the weight ratio of any anionic material to the cationic fabric softening agent is less than 0.4:1, most preferably less than 0.2:1.
  • The viscosity of the fabric softening compositions when in liquid form is preferably less than about 150 cP, most preferably less than about 120 cP. This viscosity is measured at 25'C and 110 sec -1 in a Haake Viscometer.
  • The compositions of the invention can normally be prepared by mixing the ingredients together in water, heating to a temperature of about 60°C and agitating for 5-30 minutes.
  • The invention will now be illustrated by the following non-limiting examples.
  • EXAMPLES 1 TO 6
  • Liquid fabric conditioning compositions were made up according to the formulations given in the following Table I, by mixing the ingredients together in water at about 60°C and agitating.
  • Each composition was then added to town water at the concentrations mentioned in the Table, and the pH was measured.
  • Each rinse liquor so obtained was capable of providing good fabric softening.
  • Table I also quotes the viscosity of each fabric softening composition measured in the Haake viscometer at 110 sec-1 at 25°C.
    Figure imgb0003
  • Similar results can be obtained by replacing the lanolin used in these Examples with Coronet grade lanolin (ex Croda Chemicals) or Lanolin P95 (ex Westbrook Lanolin Company).
  • Similar results can also be obtained by using as the cationic fabric softener Arquad 2T of Arquad 2HT (ex Armak Company). Still further similar results can be obtained by replacing the sodium chloride with calcium chloride, magnesium chloride or aluminium chlorhydrate.
  • EXAMPLE 7
  • Three fabric softening compositions were prepared according to the following Table.
    Figure imgb0004
  • Pieces of cotton terry cloth were treated with liquors made up from these compositions. The treated cloths were assessed by a panel of people who found that composition B gave more preferred results than either of compositions A and C.
  • EXAMPLES 8 AND 9
  • The following fabric softening compositions were prepared using lanolin-like materials in place of lanolin per se:
    Figure imgb0005
  • The pH of each of these compositions when diluted to 250 ppm was less than 7.5.
  • Notes: 1 - Distilled lanolin alcohols (ex Croda Chemicals) 2 - Iso-stearic acid (ex Emery)
  • Except as indicated otherwise, all percentages referred to herein are by weight, based on the weight of the composition.

Claims (7)

1. A method of treating fabrics comprising contacting the fabrics with an aqueous liquor having a pH less than about 7.5 and containing a cationic fabric softening agent, characterised in that said liquor also contains lanolin or a lanolin-like material and is formed by adding to water a liquid or granular solid fabric softening composition comprising a cationic fabric softening agent and lanolin or a lanolin-like material.
2. A method according to Claim 1, characterised in that the weight ratio of said lanolin or lanolin-like material to said fabric softening agent lies between 0.05:1 and 20:1.
3. A method according to Claim 2, characterised in that the weight ratio of said lanolin or lanolin-like material to said fabric softening agent lies between 0.01:1 and 10:1.
4. A method according to Claim 1, characterised in that the weight ratio of said liquor to said fabric is less than 25:1.
5. A method according to Claim 1, characterised in that the weight ratio of said liquor to said fabrics is between 10:1 and 4:1.
6. A method according to claim 1, characterised in that the liquor has such a composition and the treatment is carried out at such temperature for such a time and with such agitation that the level of cationic fabric softening agent and lanolin or lanolin-like material deposited on the fabric is less than 0.5% by weight of the dry fabric.
7. A method according to Claim 1, substantially as hereinbefore described.
EP83300624A 1982-02-10 1983-02-08 Method of softening fabrics Expired EP0086104B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AT83300624T ATE42762T1 (en) 1982-02-10 1983-02-08 PROCESS FOR SOFTENING TEXTILES.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB8203880 1982-02-10
GB8203880 1982-02-10

Publications (3)

Publication Number Publication Date
EP0086104A2 true EP0086104A2 (en) 1983-08-17
EP0086104A3 EP0086104A3 (en) 1986-02-12
EP0086104B1 EP0086104B1 (en) 1989-05-03

Family

ID=10528227

Family Applications (1)

Application Number Title Priority Date Filing Date
EP83300624A Expired EP0086104B1 (en) 1982-02-10 1983-02-08 Method of softening fabrics

Country Status (17)

Country Link
EP (1) EP0086104B1 (en)
JP (1) JPS58149379A (en)
AT (1) ATE42762T1 (en)
AU (1) AU549921B2 (en)
BR (1) BR8300642A (en)
CA (1) CA1192004A (en)
DE (1) DE3379790D1 (en)
GB (1) GB2114619B (en)
GR (1) GR78098B (en)
IN (1) IN156619B (en)
MY (1) MY8700538A (en)
NO (1) NO830420L (en)
NZ (1) NZ203172A (en)
PH (1) PH18127A (en)
PT (1) PT76217B (en)
ZA (1) ZA83877B (en)
ZW (1) ZW3483A1 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2531462A1 (en) * 1982-08-03 1984-02-10 Colgate Palmolive Co TREATMENT OF LAUNDRY AGAINST STATIC ELECTRICITY
EP0122141A2 (en) * 1983-04-08 1984-10-17 Unilever Plc Fabric softening compositions
EP0159918A2 (en) * 1984-04-19 1985-10-30 Unilever Plc Fabric softening composition
EP0607529A2 (en) * 1993-01-20 1994-07-27 Hüls Aktiengesellschaft Aqeous softeners for the treatment of textiles

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5409619A (en) * 1993-08-23 1995-04-25 Reckitt & Colman Inc. Ironing aid composition

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2202184A1 (en) * 1972-10-10 1974-05-03 Colgate Palmolive Co Fabric softening aerosol compsn - lanoline deriv, foaming agent, fluid medium and liquefied gas
DE2360408A1 (en) * 1972-12-05 1974-06-12 Unilever Nv DETERGENT COMPOSITION
US4110498A (en) * 1976-03-08 1978-08-29 The Procter & Gamble Company Fabric treatment compositions
GB2007734A (en) * 1977-10-22 1979-05-23 Cargo Fleet Chemical Co Fabric softeners
EP0013780A1 (en) * 1979-01-11 1980-08-06 THE PROCTER &amp; GAMBLE COMPANY Concentrated fabric softening composition

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2202184A1 (en) * 1972-10-10 1974-05-03 Colgate Palmolive Co Fabric softening aerosol compsn - lanoline deriv, foaming agent, fluid medium and liquefied gas
DE2360408A1 (en) * 1972-12-05 1974-06-12 Unilever Nv DETERGENT COMPOSITION
US4110498A (en) * 1976-03-08 1978-08-29 The Procter & Gamble Company Fabric treatment compositions
GB2007734A (en) * 1977-10-22 1979-05-23 Cargo Fleet Chemical Co Fabric softeners
EP0013780A1 (en) * 1979-01-11 1980-08-06 THE PROCTER &amp; GAMBLE COMPANY Concentrated fabric softening composition

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
Encyclopedia of Chemical Technology, Kirk-Othmer, 3rd ed., vol. 24, J. Wiley & Son (1984), pp. 636-639 *

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2531462A1 (en) * 1982-08-03 1984-02-10 Colgate Palmolive Co TREATMENT OF LAUNDRY AGAINST STATIC ELECTRICITY
EP0122141A2 (en) * 1983-04-08 1984-10-17 Unilever Plc Fabric softening compositions
EP0122141B1 (en) * 1983-04-08 1989-11-15 Unilever Plc Fabric softening compositions
EP0159918A2 (en) * 1984-04-19 1985-10-30 Unilever Plc Fabric softening composition
EP0159918A3 (en) * 1984-04-19 1986-12-30 Unilever Plc Fabric softening composition
EP0607529A2 (en) * 1993-01-20 1994-07-27 Hüls Aktiengesellschaft Aqeous softeners for the treatment of textiles
US5447643A (en) * 1993-01-20 1995-09-05 Huels Aktiengesellschaft Aqueous fabric softener for the treatment of textile
EP0607529B1 (en) * 1993-01-20 1998-06-24 Hüls Aktiengesellschaft Use of aqeous softeners for the treatment of textiles

Also Published As

Publication number Publication date
GB2114619A (en) 1983-08-24
GB8303394D0 (en) 1983-03-16
PT76217B (en) 1986-06-26
NO830420L (en) 1983-08-11
ATE42762T1 (en) 1989-05-15
ZW3483A1 (en) 1984-08-29
PH18127A (en) 1985-03-22
BR8300642A (en) 1983-11-08
ZA83877B (en) 1984-09-26
EP0086104A3 (en) 1986-02-12
GB2114619B (en) 1986-05-08
IN156619B (en) 1985-09-21
GR78098B (en) 1984-09-26
EP0086104B1 (en) 1989-05-03
MY8700538A (en) 1987-12-31
AU1118283A (en) 1983-08-18
AU549921B2 (en) 1986-02-20
NZ203172A (en) 1986-03-14
JPS58149379A (en) 1983-09-05
DE3379790D1 (en) 1989-06-08
CA1192004A (en) 1985-08-20
PT76217A (en) 1983-03-01

Similar Documents

Publication Publication Date Title
EP0086105B1 (en) Fabric softening composition
USRE34062E (en) Fabric softening composition contains water-insoluble surfactant and aliphatic mono-carboxylic acid
CA1143512A (en) Concentrated fabric softening composition
EP0122141B1 (en) Fabric softening compositions
EP0060003B1 (en) Textile treatment compositions and preparation thereof
EP1062312B1 (en) Fabric conditioning concentrate
US4844823A (en) Fabric softener composition containing di-esterified long chain fatty acid quaternary ammonium salt
US5407588A (en) Fabric softening composition
US4464272A (en) Fabric softening composition
EP1283859B1 (en) Process for preparing a fabric conditioning composition
EP0086104B1 (en) Method of softening fabrics
EP0125031A1 (en) Liquid fabric-softening composition
EP0088520B1 (en) Fabric softening composition
CA2021128C (en) Fabric softening composition
EP0159918A2 (en) Fabric softening composition
JP2000507653A (en) Use of fabric softener composition
MXPA99008521A (en) Super-concentrated liquid rinse cycle 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

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

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

AK Designated contracting states

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

17P Request for examination filed

Effective date: 19860118

17Q First examination report despatched

Effective date: 19870422

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

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

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

Ref country code: BE

Effective date: 19890503

Ref country code: AT

Effective date: 19890503

REF Corresponds to:

Ref document number: 42762

Country of ref document: AT

Date of ref document: 19890515

Kind code of ref document: T

REF Corresponds to:

Ref document number: 3379790

Country of ref document: DE

Date of ref document: 19890608

ITF It: translation for a ep patent filed

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

ET Fr: translation filed
PLBI Opposition filed

Free format text: ORIGINAL CODE: 0009260

26 Opposition filed

Opponent name: HENKEL KOMMANDITGESELLSCHAFT AUF AKTIEN

Effective date: 19900112

NLR1 Nl: opposition has been filed with the epo

Opponent name: HENKEL KOMMANDITGESELLSCHAFT AUF AKTIEN.

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

Ref country code: DE

Payment date: 19910328

Year of fee payment: 9

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

Ref country code: FR

Payment date: 19920110

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: 19920120

Year of fee payment: 10

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

Ref country code: CH

Payment date: 19920121

Year of fee payment: 10

RDAG Patent revoked

Free format text: ORIGINAL CODE: 0009271

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

Free format text: STATUS: PATENT REVOKED

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

Ref country code: NL

Payment date: 19920229

Year of fee payment: 10

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

27W Patent revoked

Effective date: 19911115

NLR2 Nl: decision of opposition
EUG Se: european patent has lapsed

Ref document number: 83300624.0

Effective date: 19920401