WO1997020099A1 - Cleaning method for textile fabrics - Google Patents

Cleaning method for textile fabrics Download PDF

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Publication number
WO1997020099A1
WO1997020099A1 PCT/US1996/019171 US9619171W WO9720099A1 WO 1997020099 A1 WO1997020099 A1 WO 1997020099A1 US 9619171 W US9619171 W US 9619171W WO 9720099 A1 WO9720099 A1 WO 9720099A1
Authority
WO
WIPO (PCT)
Prior art keywords
stain
spot
absorbent
textile fabric
water
Prior art date
Application number
PCT/US1996/019171
Other languages
English (en)
French (fr)
Inventor
Eric Tcheou
Jose Luis Vega
Original Assignee
The Procter & Gamble Company
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 claimed from PCT/US1996/014821 external-priority patent/WO1997020098A1/en
Application filed by The Procter & Gamble Company filed Critical The Procter & Gamble Company
Priority to BR9611771A priority Critical patent/BR9611771A/pt
Priority to DE69628464T priority patent/DE69628464D1/de
Priority to US09/077,284 priority patent/US6048368A/en
Priority to AT96943549T priority patent/ATE241691T1/de
Priority to AU12766/97A priority patent/AU1276697A/en
Priority to EP96943549A priority patent/EP0910619B1/en
Priority to JP09520730A priority patent/JP3093279B2/ja
Publication of WO1997020099A1 publication Critical patent/WO1997020099A1/en
Priority to NO982358A priority patent/NO982358L/no

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Classifications

    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06F—LAUNDERING, DRYING, IRONING, PRESSING OR FOLDING TEXTILE ARTICLES
    • D06F43/00—Dry-cleaning apparatus or methods using volatile solvents
    • D06F43/002—Spotting apparatus
    • A—HUMAN NECESSITIES
    • A47—FURNITURE; DOMESTIC ARTICLES OR APPLIANCES; COFFEE MILLS; SPICE MILLS; SUCTION CLEANERS IN GENERAL
    • A47L—DOMESTIC WASHING OR CLEANING; SUCTION CLEANERS IN GENERAL
    • A47L25/00—Domestic cleaning devices not provided for in other groups of this subclass 
    • A47L25/08—Pads or the like for cleaning clothes
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02—Anionic compounds
    • C11D1/37—Mixtures of compounds all of which are anionic
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66—Non-ionic compounds
    • C11D1/825—Mixtures of compounds all of which are non-ionic
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0008—Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
    • C11D17/0017—Multi-phase liquid compositions
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
    • C11D17/041—Compositions releasably affixed on a substrate or incorporated into a dispensing means
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/43—Solvents
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D2111/00—Cleaning compositions characterised by the objects to be cleaned; Cleaning compositions characterised by non-standard cleaning or washing processes
    • C11D2111/10—Objects to be cleaned
    • C11D2111/12—Soft surfaces, e.g. textile

Definitions

  • the present invention relates to a method of removing spots and stains from textile fabrics.
  • stains are not always effectively removed by conventional laundry cleaning processes, for example in a washing machine. Such stains may be more effectively removed by pre-treatment, which herein means a cleaning treatment carried out before the conventional laundry cleaning process; and/or by post-treatment, which herein means a cleaning treatment carried out after the conventional laundry cleaning process.
  • pre-treatment herein means a cleaning treatment carried out before the conventional laundry cleaning process
  • post-treatment which herein means a cleaning treatment carried out after the conventional laundry cleaning process.
  • the present invention is concerned with a post-treatment cleaning method.
  • EP200807 published on 12th November 1986, discloses an iron intended for cleaning clothes during ironing, i.e. a post-treatment.
  • the housing of the iron can be adapted with a recess to receive a brush (page 3, line 22 to page 4, line 1) .
  • the iron is also provided with vacuum cleaning means. There is no suggestion that cleaning compositions could be used to enhance the cleaning method.
  • the object of the present invention is to provide a more effective method of treating a spot or stain on a textile fabric comprising the steps of: applying a detergent composition to the spot or stain; placing an absorbent layer adjacent to one side of the textile fabric in the region of the spot or stain; and applying heat, pressure, or heat and pressure so that some or all of the spot or stain is absorbed into the absorbent layer.
  • the textile fabric should be dry and ready to wear at the end of the cleaning method.
  • the object of the invention is achieved by applying the heat and/or pressure to the opposing side of the textile fabric in the region of the spot or stain preferably in the presence of a hydrophilic solvent or water.
  • a hydrophilic solvent or water preferably in the presence of a hydrophilic solvent or water.
  • the second means for transferring the stain to the absorbent layer is preferably by applying heat, more preferably by using a hand-held domestic iron.
  • the first means for transferring some or all of the spot or stain preferably comprises the step of rubbing, pressing or brushing the spot or stain.
  • Fig 1 shows the top and longitudinal view of a container with a foam pad secured to its cap.
  • the cap has a small central opening through which the liquid can pass.
  • Fig 2 shows the top and longitudinal view of a container with a brush secured to its cap.
  • the crap has a small central opening through which the liquid can pass.
  • Fig 3 shows the top and longitudinal view o:i a container with a convex shaped polypropylene porous pad.
  • the pad has pore size ranging from 300 to 700 micrometers.
  • Fig 4 shows the top and longitudinal view o:: a container with a convex shaped polypropylene po:rous pad and a supporting plate which has a plurality of holes which restricts the amount of liquid that passes through the porous material.
  • the pad has pore size ranging from 300 to 700 micrometers.
  • Fig 5 shows the top and longitudinal view of a container with a roll-on type extremity.
  • Fig 6 shows the top and longitudinal view of a container with a piston-type extremity. Upon pressing of the tip of the piston against a fabric surface, a liquid is released from within the container onto the fabric.
  • Fig 7 shows the longitudinal view of a conventional container with an elongated extremity, used to apply liquid on surfaces.
  • Fig 8 shows a hand-operated device having sponge-type first and second treatment members.
  • Fig 9 shows a hand-operated device having a bristled protuberances comprising the first treatment member and a disposable sponge as a second treatment member.
  • Fig 10 shows a hand-operated device with the first and second treatment members comprising looped protuberances.
  • a most preferred cleaning method comprises the steps of : (a) applying a detergent composition to a spot or stain and placing an absorbent layer adjacent to the textile fabric in the region of the spot or stain and a first means for transferring some or all of the spot or stain into the absorbent layer; and subsequently (b) applying a hydrophilic solvent, or water, to the textile fabric in the region of the spot or scain and placing an absorbent layer adjacent to the textile fabric in the region of the spot or stain and the step of applying heat to the textile fabric in the region of the spot or stain.
  • the application of heat or pressure, or both, may be achieved by any means, but is most preferably achieved by a hand-held device such as an iron.
  • a conventional iron having a hot-plate fixed to a body is a highly preferred hand held device.
  • the hot ⁇ plate is heated most commonly by electrical means, and may have a means for controlling the temperature.
  • a supply of water or steam may also be provided by the iron.
  • the absorbent layer is placed on a flat surface, such as an ironing board, and the stained or soiled textile fabric is laid flat on top of, and in contact with, the absorbent layer.
  • the iron can then be easily applied to the textile fabric in the region of the stain or spot in order to ensure complete, or substantially complete, transfer of the stain or spot into the absorbent layer.
  • the iron is preferably operated at a temperature of from 40°C to 180"C.
  • An alternative device for applying heat or pressure is a heated roller or any other heated applicator.
  • the roller or applicator may also be provided with a supply of the detergent composition.
  • Suitable applicators include a steam iron with suction brush attachment, such as that disclosed in EP-A-0 493 348, and a thermoelectric applicator, such as that disclosed in EP-A-0 552 397. Also suitable is a steam iron with atomiser, such as that disclose in EP-A-0 629 736 wherein the detergent composition may optionally be stored in the iron and delivered directly onto the textile fabrics by means of the atomiser.
  • hydrophobic stains are first rendered hydrophilic by applying a detergent composition, optionally with a gentle rubbing action; water is then applied to the stain, again, optionally with a gentle rubbing action.
  • the stain is removed by laying the stained fabric adjacent to an absorbent layer.
  • the stain which has been rendered more hydrophilic by the treatment, is transferred to the absorbent layer.
  • Textile fabrics are any materials made from cloth, including garments such as shirts, blouses, socks, skirts, trousers, jackets, underwear etc, and also including tablecloths, towels, curtains etc.
  • the definition of textile fabrics as used herein does not include carpets and similar floor coverings.
  • Textile fabrics which are to be used in the present invention are commonly made by weaving or knitting. Many different fibres may be used to produce woven, knitted or other types of textile fabric including synthetic fibres (such as polyester, polyamide, etc.) and natural fibres from plants (such as cotton, hemp) and from animals (such as wool, angora, silk) . Blends of different fibres are also commonly used.
  • a highly preferred component of the detergent composition for use herein is a solvent. More preferred solvents are defined in terms of Hansen parameters.
  • a hydrophobic solvent as defined herein is considered to be a solvent having Hansen hydrogen bonding cohesion parameter dH below 18 (Joule/cm 3 ) 0 - 5 .
  • Preferred hydrophobic solvents have a Hansen hydrogen bonding cohesion parameter dH below 12 (Joule/cm 3 ) u •5 and a Hansen polar parameter dP below 8 (Joule/cm 3 ) 0 - 5 .
  • Preferred solvents for use comprise mixtures of hydrocarbons with a flash point no lower than 70°C, an initial boiling point no lower than 130°C and a solidification point not above 20°C and aliphatic fatty acid esters. More preferred solvents would be alkanes or alkenes with a chain length above C7, and particularly alkanes and alkenes with an average of C8 to C20 atoms. Particularly preferred hydrophobic solvents are deodorised kerosine; solvent naphta; chlorinated hydrocarbons; and terpenes.
  • Solvents are used in the detergent compositions of the present invention preferably at a level of from 3% to 90%, more preferably from 4% to 45%, and most preferably from 5% to 25% by weight of the detergent composition.
  • solvents having a Hansen parameter of dH less than 18 (Joule/cm 3 ) 0 * 5 include glycol ethers, more preferably glycol ethers based upon ethylene oxide, propylene oxide, or mixtures thereof. Particularly preferred are ethylene glycol monoethyl ether; Propylene glycol monomethyl ether; 2-butoxy ethanol; butyl diethylene glycol ether ethanol; butoxytriglycol; butylene glycol; hexylene glycol; and propyl propanol. Such solvents may, and preferably are, used in combination with either short chain surfactants, long chain surfactants, or mixtures thereof.
  • hydrophobic solvents defined above are used in combination with mixtures of short chain and long chain surfactants having preferably an overall HLB value of from 2 to 16, and more preferably from 8 to 14.
  • Preferred molar ratio of short-chain to long chain ratios are from 1:10 to 10:1, more preferably between 1:3 and 3:1, most preferably about 1:1.
  • Surfactants are preferably present at a level of from 1 to 50%, more preferably 10 to 40% and most preferably 15 to 30% by weight of the detergent composition.
  • Short chain surfactants are surfactants which comprise a C6-C10 alkyl chain as their hydrophobic portion.
  • Preferred short-chain surfactants for use are the C4-C8 fatty alcohol polyglycol ethers with 2-5 EO.
  • C6-C8 alkyl sulphonates, C6-C8 alkyl sulphates, C6-C8 alkyl ethoxy sulphates, C6-C10 betaines or C6-C10 amine oxides could also be useful.
  • Long-chain surfactants useful in the detergent compositions of the present invention include the following.
  • Water-soluble salts of the higher fatty acids are useful anionic surfactants in the compositions herein.
  • Soaps can be made by direct saponification of fats and oils or by the neutralization of free fatty acids.
  • Particularly useful are the ethanolamine, sodium and potassium salts of the mixtures of fatty acids derived from coconut oil and tallow, i.e., monoethanolamine, sodium or potassium tallow and coconut soap.
  • Useful anionic surfactants also include the water- soluble salts, preferably the alkali metal, ethanolamine, ammonium and alkylolammonium salts, of organic sulfuric reaction products having in their molecular structure an alkyl group containing from about 10 to about 20 carbon atoms and a sulfonic acid or sulfuric acid ester group.
  • alkyl is the alkyl portion of acyl groups.
  • alkyl sulfates especially those obtained by sulfating the higher alcohols carbon atoms
  • alkyl benzene sulfonates in which the alkyl group contains from about 9 to about 15 carbon atoms, in straight or branched chain configuration, e.g., those of the type described in U.S. Pat. Nos. 2,220,099 and 2,477,383; and methyl ester sulphonates.
  • linear straight chain alkyl benzene sulfonates in which the average number of carbon atoms in the alkyl group is from about 11 to 13, abbreviated as C11-C13 LAS.
  • alkyl glyceryl ether sulfonates especially those ethers of higher alcohols derived from tallow and coconut oil; coconut oil fatty acid monoglyceride sulfonates and sulfates; salts of alkyl phenol ethylene oxide ether sulfates containing from about 1 to about 10 units of ethylene oxide per molecule and wherein the alkyl groups contain from about 8 to about 12 carbon atoms; and salts of alkyl ethylene oxide ether sulfates containing from about 1 to about 10 units of ethylene oxide per molecule and wherein the alkyl group contains from about 10 to about 20 carbon atoms.
  • Other useful anionic surfactants herein include the water-soluble salts of esters of alpha-sulfonated fatty acids containing from about 6 to 20 carbon atoms in the fatty acid group and from about 1 to 10 carbon atoms in the ester group; water-soluble salts of 2-acyloxy- alkane-l-sulfonic acids containing from about 2 to 9 carbon atoms in the acyl group and from about 9 to about 23 carbon atoms in the alkane moiety; alkyl ether sulfates containing from about 10 to 20 carbon atoms in the alkyl group and from about 1 to 30 moles of ethylene oxide; watersoluble salts of olefin sulfonates containing from about 12 to 24 carbon atoms; and beta- alkyloxy alkane sulfonates containing from about 1 to 3 carbon atoms in the alkyl group and from about 8 to about 20 carbon atoms in the alkane moiety.
  • Water-soluble nonionic surfactants are also useful as surfactants in the compositions of the invention. Indeed, preferred processes use anionic/nonionic blends.
  • Such nonionic materials include compounds produced by the condensation of alkylene oxide groups (hydrophilic in nature) with an organic hydrophobic compound, which may be aliphatic or alkyl aromatic in nature. The length of the polyoxyalkylene group which is condensed with any particular hydrophobic group can be readily adjusted to yield a water-soluble compound having the desired degree of balance between hydrophilic and hydrophobic elements.
  • Suitable nonionic surfactants include the polyethylene oxide condensates of alkyl phenols, e.g., the condensation products of alkyl phenols having an alkyl group containing from about 6 to 16 carbon atoms, in either a straight chain or branched chain configuration, with from about 4 to 25 moles of ethylene oxide per mole of alkyl phenol.
  • Preferred nonionics are the water-soluble condensation products of aliphatic alcohols containing from 8 to 22 carbon atoms, in either straight chain or bra.nched configuration, with from 1 to 25 moles of ethylene oxide per mole of alcohol, especially 2 to 7 moles of ethylene oxide per mole of alcohol.
  • Particularly preferred are the condensation products of alcohols having an alkyl group containing from about 9 to 15 carbon atoms; and condensation products of propylene glycol with ethylene oxide.
  • polyhydroxy fatty acid amides which may be prepared by reacting a fa.tty acid ester and an N-alkyl polyhydroxy amine.
  • the preferred amine for use in the present invention is N-IR1)- CH2 (CH20H)4-CH2-OH and the preferred ester is a C12-C20 fatty acid methyl ester.
  • Most preferred is the reaction product of N-methyl glucamine (which may be derived from glucose) with C12-C20 fatty acid methyl ester.
  • Semi-polar nonionic surfactants include water-soluble amine oxides containing one alkyl moiety of from about 10 to 18 carbon atoms and 2 moieties selected from the group consisting of alkyl groups and hydroxyalkyl groups containing from 1 to about 3 carbon atoms; w ⁇ tter-soluble phosphine oxides containing one alkyl moiety of about 10 to 18 carbon atoms and 2 moieties selected from the group consisting of alkyl groups and hydroxyctlkyl groups containing from about 1 to 3 carbon atoms; and water- soluble sulfoxides containing one alkyl moiety of from about 10 to 18 carbon atoms and a moiety selected from the group consisting of alkyl and hydroxyalkyl moieties of from about 1 to 3 carbon atoms.
  • Ampholytic surfactants include derivatives of aliphatic or aliphatic derivatives of heterocyclic secondary and tertiary amines in which the aliphatic moiety can be either straight or branched chain and wherein one of the aliphatic substituents contains from about 8 to 18 carbon atoms and at least one aliphatic substituent contains an anionic water-solubilizing group.
  • Zwitterionic surfactants include derivatives of aliphatic quaternary ammonium phosphonium, and sulfonium compounds in which one of the aliphatic substituents contains from about 8 to 18 carbon atoms.
  • Useful cationic surfactants include water-soluble quaternary ammonium compounds of the form R4R5RgR N + X " , wherein R4 is alkyl having from 10 to 20, preferably from 12-18 carbon atoms, and R5, Rg and R7 are each C ⁇ _ to C ⁇ alkyl preferably methyl; X " is an anion, e.g. chloride.
  • Examples of such trimethyl ammonium compounds include C12-14 alkyl trimethyl ammonium chloride and cocalkyl trimethyl ammonium methosulfate.
  • surfactants that may be used in the compositions of the present invention include C10-C18 glycerol ethers, CIO-18 alkyl polyglycoside and their corresponding sulphated polyglycosides, alkyl ester sulphonates, and oleoyl sarcosinate.
  • Enzymes can also be incorporated into the composition of the present invention.
  • the composition of the present invention can contain neutral or alkaline salts which have a pH in solution of seven or greater, and can be either organic or inorganic in nature. While some of the salts are inert, many of them also function as detergency builder materials in the laundering solution.
  • neutral water-soluble salts examples include the alkali metal, ethanolamine, ammonium or substituted ammonium chlorides, fluorides and sulfates.
  • the sodium, ethanolamine and ammonium salts of the above are preferred.
  • Citric acid and, in general, any other organic or inorganic acid may be incorporated into the present invention.
  • water-soluble salts include the compounds commonly known as detergent builder materials.
  • Builders are generally selected from the various water-soluble, alkali metal, ethanolamine, ammonium or substituted ammonium phosphates, polyphosphates, phosphonates, polyphosphonates, carbonates, silicates, bora es, and polyhydroxysulfonates.
  • Preferred are the sodium, ethanolamine and ammonium salts of the above.
  • inorganic phosphate builders are sodium and potassium tripolyphosphate, pyrophosphate, polymeric metaphosphate having a degree of polymerization of from about 6 to 21, and orthophosphate.
  • polyphosphonate builders are the salts of ethylene diphosphonic acid, ;he salts of ethane 1-hydroxy-1, 1-diphosphonic acid and the salts of ethane, 1, 1, 2-triphosphonic acid.
  • Other p.iosphorus builder compounds are disclosed in U.S. Pat. itfos. 3,159,581; 3,213,030; 3,422,021; 3,422,137; 3,400,176 and 3,400,148, incorporated herein by reference. In general, however, phosphates are preferably avoided for environmental reasons.
  • nonphosphorus, inorganic builders are sodium and potassium carbonate, bicarbonate, sesquicarbonate, tetraborate decahydrate, and silicate having a molar ratio of Si ⁇ 2 to alkali metal oxide of from about 0.5 to about
  • the detergent composition used herein is in liquid form, comprising active components selected from those described above, the balance of the detergent composition, typically from 5% to 92% by weight, consisting of water.
  • the preferred viscosity of the detergent composition is from 1 to 10000 mPa.s, more preferably from 1 to 4000 mPa.s, and most preferably from 1 to 300 mPa.s.
  • Hydrophilic solvents for use herein are considered to be those solvents having a Hansen parameter of either dH more than 18 (Joule/cm 3 ) 0 - 5 , or dp more than 8 (Joule/cm 3 ) 0 - 5 .
  • Preferred hydrophilic solvents are: water (including aqueous solutions); alcohol (ethanol, IPA) ; glycol ethers including diethylene glycol, triethylene glycol and ethylene glycol; ethylene cyanohydrin; ethanol amine and triethanolamine.
  • Bleaching agents may also be useful in the method of the present invention for treating bleachable stains .
  • the bleaching agents may be incorporated into the compositions described above, or may be added as separate bleaching compositions. Peroxide bleaching agents are most preferred. Absorbent layers
  • absorbent layers refers to materials which absorb and contain fluids.
  • the absorbent layer may be any absorbent means which is generally compressible, conformable, and capable of absorbing and retaining liquids.
  • the absorbent pad may be manufactured in a wide variety of sizes and shapes (e.g., rectangular, round, asymmetric, etc.) .
  • suitable absorbent materials include comminuted wood pulp, creped cellulose wadding; meltblown polymers; chemically stiffened, modified or cross-linked cellulosic fibers; tissue including tissue wraps and tissue laminates; absorbent foams; absorbent sponges; superabsorbent polymers; absorbent gelling materials; or any equivalent material or combinations of materials.
  • the configuration and construction of the absorbent pad may also be varied (e.g., the absorbent pad may have varying caliper zones, a hydrophilic gradient, a superabsorbent gradient, or lower average density and lower average basis weight acquisition zones; or may comprise one or more layers or structures) . Further, the size and absorbent capacity of the absorbent pad may be varied.
  • the absorbent layer can include a backsheet which can be either liquid permeable (poly film) or not (e.g. non-woven, too) .
  • a backsheet which can be either liquid permeable (poly film) or not (e.g. non-woven, too) .
  • the backsheet is a poly film, the following applies :
  • the poly backsheet is positioned on the bottom surface of the absorbent pad and is preferably joined thereto by attachment means such as those well known from the manufacture of disposable articles.
  • the backsheet may be secured to the absorbent pad by a uniform continuous layer of adhesive, a patterned layer of adhesive, or an array of separate lines, spirals, or spots of adhesive. Adhesives which have been found to be satisfactory are manufactured by H. B. Fuller Company of St. Paul, Minnesota and marketed as HL-1258.
  • the attachment means will preferably comprise an open pattern network of filaments of adhesive as is disclosed in U.S. Patent 4,573,986 entitled "Disposable Waste-Containment Garment", which issued to Minetola et al. on March 4, 1986, more preferably several lines of adhesive filaments swirled into a spiral pattern such as is illustrated by the apparatus and methods shown in U.S. Patent 3,911,173 issued to Sprague, Jr. on October 7, 1975; U.S. Patent 4,785,996 issued to Ziecker, et al. on November 22, 1978; and U.S. Patent 4,842,666 issued to Werenicz on June 27, 1989.
  • the attachment means may comprise heat bonds, pressure bonds, ultrasonic bonds, dynamic mechanical bonds, or any other suitable attachment means or combinations of these attachment means as are known in the art .
  • the backsheet is impervious to liquids and is preferably manufactured from a thin, heat resistant, plastic film, although other flexible liquid impervious materials may also be used.
  • the backsheet prevents the liquids absorbed and contained in the absorbent pad from wetting underlying materials.
  • the backsheet may thus comprise a woven or nonwoven material, polymeric films such as thermoplastic films of polyethylene or polypropylene, or composite materials such as a film- coated nonwoven material .
  • the absorbent layer may include a topsheet or outer, protective layer.
  • the topsheet is liquid pervious permitting liquids to readily penetrate through its thickness.
  • the characteristics of this outer protective layer includes : - that it be of appropriate design to substantially prevent loss or transfer of fibers of the inner sorbent material outwardly there through,
  • a suitable topsheet may be manufactured from a wide range of materials, such as porous foams; reticulated foams; apertured plastic films; or woven or nonwoven webs of natural fibers (e.g., wood or cotton fibers) , synthetic fibers (e.g., polyester or polypropylene fibers) , or a combination of natural and synthetic fibers.
  • this topsheet may be a nonwoven web of fibers spunbonded, carded, wet-laid, meltblown, hydroentangled, combinations of the above, or the like.
  • a preferred topsheet is carded and thermally bonded by means well known to those skilled in the fabrics art .
  • a preferred topsheet comprises a web of staple length polypropylene fibers such as is manufactured by Veratec, Inc:., a Division of International Paper Company, of Walpole, Massachusetts under the designatiion P-8.
  • Another usable non woven material is manufactured from Crown Zellerbach of Camas, under the trade nane Celestra.
  • the absorbent structure is located between the topsheet and the backsheet, and might comprise these two as in integral element. It can be produced from a wide variety of liquid-absorbent materials, such as also commonly used in disposable hygienic articles, such as diapers, catamenials or Adult incontinence articles.
  • Exemplary absorbent structures for use as absorbent layer as used in the disposable industry are described in U.S. Patent 4,610,678 entitled “High-Density Absorbent Structures” issued to Weisman et al. on September 9, 1986; U.S. Patent 4,673,402 entitled “Absorbent Articles With Dual-Layered Cores” issued to Weisman et al. on June 16, 1987; U.S. Patent 4,888,231 entitled “Absorbent Core Having A Dusting Layer” issued to Angstadt on December 19, 1989; and U.S. Patent 4,834,735, entitled “High Density Absorbent Members Having Lower Density and Lower Basis Weight Acquisition Zones", issued to Alemany et al. on May 30, 1989.
  • Other absorbent pad designs are described in European Patent Application No.'s 93305150.0 and 93309614.1.
  • Exemplary designs comprise the use of fibrous (e.g. cellulosic) materials in combination with "Superabsorbent materials", essentially hydrogel forming materials.
  • Absorbent gelling materials are extensively used in absorbent hygiene articles such as diapers or sanitary napkins, due to their high absorption capacity for liquids, which may typically range from 15 g per gram to about 50 g/g.
  • the gelling material is most often applied in particulate form in particle sizes ranging from 20 to 2000 micrometers.
  • EP-A-0 407 838 discloses a gel-forming material for use in foodstuffs, which comprises a mixture of a crosslinked polymer and a non-crosslinked polymer for lump-free solution in water.
  • EP-A-0 278 601 discloses a mixture of an absorbent gelling polymer, such as formed from water-soluble, ethylenically unsaturated monomers or crosslinked products thereof, including acrylic acid or a salt of acrylic acid as the main component, and inorganic material such as aluminia, or silica.
  • the polymers in the mixture may be comprised of any combination of two or more chemically different types.
  • the disclosed absorbent mixture is suited to absorb both low-viscosity and high-viscosity liquids.
  • WO 91/12029 discloses an odor control composition comprising aggregated absorbent gelling material particles and zeolite material.
  • the absorbent gelling material is made of hydrolized acrylonitrile grafted starch, acrylic acid grafted starch, polyacrylates, malice anhydride-based copolymers and combinations thereof.
  • US patent No 4,333,464 discloses a sanitary napkin having water absorbent polymer which may comprise a mixture of two types of absorbent gelling material from the group consisting of starch, ⁇ -hydroxyethy acrylate, acrylonitrile, acrylic acid and acrylamide, carboxymethylcellulose, hydrophilic copolymer3 of acrylates, copolymers of a vinyl ester and an ethylenically unsaturated carboxylic acid and their saponification products, polyvinyl alcohol, and its derivatives.
  • water absorbent polymer which may comprise a mixture of two types of absorbent gelling material from the group consisting of starch, ⁇ -hydroxyethy acrylate, acrylonitrile, acrylic acid and acrylamide, carboxymethylcellulose, hydrophilic copolymer3 of acrylates, copolymers of a vinyl ester and an ethylenically unsaturated carboxylic acid and their saponification products, polyvinyl alcohol, and its derivatives.
  • US patent no 4,902,544 discloses a flexible tibular casing comprising a crosslinked hydrocolloid .and naturally occurring cellulose such as saw dust, crushed corncobs, cottonlinters, wood pulp and the luce, ion- exchange resins or clay minerals.
  • GB-B-1 544 002 discloses a mixture of a salt of an acrylic acid polymer and either guar gum, alginates or xanthan gum to provide an absorbent material with good absorbent properties, irrespective of the presence of an electrolyte in the liquid to be absorbed. Polyvalent ions may be incorporated in the absorbent composite.
  • US patent no 4,411,660 discloses in an absorbent product two layers of absorbent material of different types, such that the upper layer gels slower than the first layer.
  • EP-B-0 401 189 discloses that favourable properties of absorbent products can be achieved by using two different types of absorbent gelling material in separate layers, rather than as a mixture of the two absorbent gelling materials in a single layer.
  • the hydrogel-forming absorbent polymers useful in the present invention include a variety of substantially water-insoluble, but water-swellable polymers capable of absorbing large quantities of liquids. Such polymers materials are also commonly referred to as "hydrocolloids", or “superabsorbent” materials. These hydrogel-forming absorbent polymers preferably have a multiplicity of anionic, functional groups, such as sulfonic acid, and more typically carboxy, groups. Examples of polymers suitable for use herein include those which are prepared from polymerizable, unsaturated, acid-containing monomers. Thus, such monomers include the olefinically unsaturated acids and anhydrides that contain at least one carbon to carbon olefinic double bond. More specifically, these monomers can be selected from olefinically unsaturated carboxylic acids and acid anhydrides, olefinically unsaturated sulfonic acids, and mixtures thereof.
  • non-acid monomers can also be included, usually in minor amounts, in preparing the hydrogel-forming absorbent polymers herein.
  • Such non-acid monomers can include, for example, the water-soluble or water- dispersible esters of the acid-containing monomers, as well as monomers that contain no carboxylic or sulfonic acid groups at all.
  • Optional non-acid monomers can thus include monomers containing the following types of functional groups: carboxylic acid or sulfonic acid esters, hydroxyl groups, amide-groups, amino groups, nitrile groups and quaternary ammonium salt groups.
  • These non-acid monomers are well-known materials and are described in greater detail, for example, in U.S. Patent 4,076,663 (Masuda et al) , issued February 28, 1978, and in U.S. Patent 4,062,817 (Westerman) , issued December 13, 1977, both of which are incorporated by reference.
  • Olefinically unsaturated carboxylic acid and carboxylic acid anhydride monomers include the acrylic acids typified by acrylic acid itself, methacrylic acid, ethacrylic acid, -chloroacrylic acid, a-cyanoacrylic acid, -methylacrylic acid (crotonic acid) , - phenylacrylic acid, -acryloxypropionic acid, sorbic acid, -chlorosorbic acid, angelic acid, cinnstmic acid, p-chlorocinnamic acid, -sterylacrylic acid, itaconic acid, citroconic acid, mesaconic acid, glutaconic acid, aconitic acid, maleic acid, fumaric acid, tricarboxyethylene and maleic acid anhydride.
  • acrylic acids typified by acrylic acid itself, methacrylic acid, ethacrylic acid, -chloroacrylic acid, a-cyanoacrylic acid, -methylacrylic acid (crotonic acid
  • Olefinically unsaturated sulfonic acid monomers include aliphatic or aromatic vinyl sulfonic acids such as vinylsulfonic acid, alkyl sulfonic acid, vinyl toluene sulfonic acid and styrene sulfonic acid; acrylic and methacrylic sulfonic acid such as sulfoethyl acrylate, sulfoethyl methacrylate, sulfopropyl acrylate, sulfopropyl methacrylate, 2-hydroxy-3-methacryloxypropyl sulfonic acid and 2-acrylamide-2-methylproparte sulfonic acid.
  • vinylsulfonic acid alkyl sulfonic acid, vinyl toluene sulfonic acid and styrene sulfonic acid
  • acrylic and methacrylic sulfonic acid such as sulfoethyl acrylate, sulfoeth
  • Preferred hydrogel-forming absorbent polymers for use in the present invention contain carboxy groups. These polymers include hydrolyzed starch-acrylonitrile graft copolymers, partially neutralized starch- acrylonitrile graft copolymers, starch-acrylic acid graft copolymers, partially neutralized starch-acrylic acid graft copolymers, saponified vinyl acetate-acrylic ester copolymers, hydrolyzed acrylonitrile or acrylamide copolymers, slightly network crosslinked polymers of any of the foregoing copolymers, partially neutralized polyacrylic acid, and slightly network crosslinked polymers of partially neutralized polyacrylic acid.
  • polymers can be used either solely or in the form of a mixture of two or more different polymers. Examples of these polymer materials are disclosed in U.S. Patent 3,661,875, U.S. Patent 4,076,663, U.S. Patent 4,093,776, U.S. Patent 4,666,983, and U.S. Patent 4,734,478.
  • hydrogel-forming particles are slightly network crosslinked polymers of partially neutralized polyacrylic acids and starch derivatives thereof.
  • the hydrogel-forming particles comprise from about 50 to about 95%, preferably about 75%, neutralized, slightly network crosslinked, polyacrylic acid (i.e. poly (sodium acrylate/acrylic acid)) .
  • the hydrogel-forming absorbent polymers are preferably slightly network crosslinked.
  • Network crosslinking serves to render the polymer substantially water-insoluble and, in part, determines the absorptive capacity and extractable polymer content characteristics of the precursor particles and the resultant macrostructures. Processes for network crosslinking the polymers and typical network crosslinking agents are described in greater detail in the hereinbefore-referenced U.S. Patent 4,076,663, and in DE-A-4020780 (Dahmen) .
  • hydrogel-forming absorbent polymers can have a size varying over a wide range, specific particle size distributions and sizes are preferred.
  • particle size is defined for hydrogel-forming absorbent polymers that do not have a large greatest dimension/smallest dimension ratio such as fibers (e.g., granules, flakes, or pulverulents) as the dimension of a precursor particle that is determined by sieve size analysis.
  • a hydrogel-forming absorbent polymer particle that is retained on a standard #30 sieve with 600 micron openings is considered to have a particle size greater than 600 microns
  • a hydrogel-forming absorbent: polymer particle that passes through the #30 sieve with 600 micron openings and is retained on a standard #35 sieve with 500 micron openings is considered to have; a particle size between 500 and 600 microns
  • a hydrogel-forming absorbent polymer particle that passes through a #35 sieve with 500 micron openings is considered to have a particle size less than 500 microns.
  • the particles will generally range in size from about 1 micron to about 2000 microns, more preferably from about. 20 microns to about 1000 microns.
  • the mass median particle size of the hydrogel-forming absorbent polymers is important in determining the chareicteristics and properties of the resultant particles.
  • The; mass median particle size of a given sample of hydrogel- forming absorbent polymer particles is defined as the particle size that divides a sample in half on a mass basis.
  • the mass average particle size could be specified as a measure for the dimension of the particles, wherein the mass average particle size is the average particle size of the sample on a mass basis.
  • the mass median particle size of the hydrogel-forming absorbent polymer particles will generally be from about: 20 microns to about 1500 microns, more preferably from about 50 microns to about 1000 microns.
  • the particles have a mass median particle size less than about 1000 microns, more preferably less than about 600 microns, most preferably less than about 500 microns.
  • the particle size of materials having a large greatest dimension/smallest dimension such as fibers is typically defined by their largest dimension.
  • the length of the fibers is used to define the "particle size.”
  • the denier and/or the diameter of the fibers can also be specified.
  • the fibers have a length greater than about 5 mm, preferably between about 10 mm and about 100 mm, more preferably between about 10 mm and about 50 mm.
  • Preferred hydrogel-forming absorbent polymer particles of the present invention are those which exhibit a high absorptive capacity or Teabag Centrifuge Capacity value.
  • Absorptive capacity, or Teabag Centrifuge Capacity refers to the capacity of a given polymer to absorb liquids with which it comes into contact under free-swelling conditions. TCC can vary significantly with the nature of the liquid being absorbed and with the manner in which the liquid contacts the polymer material .
  • Teabag Centrifuge Capacity is defined in terms of the amount of 0.9 % saline solution absorbed by any given polymer in terms of grams of saline solution per gram of polymer material in a Tea bag Centrifuge Capacity test procedure hereinafter defined in the Test Methods section.
  • Preferred hydrogel-forming absorbent polymer particles of the present invention are those which have Teabag Centrifuge Capacity values of at least about 20 grams, more preferably at least about 25 grams, of saline solution per gram of polymer material.
  • the hydrogel-forming absorbent polymer particles useful herein have Teabag Centrifuge Capacity values of from about 20 grams to about 70 grams of saline solution per gram of polymer. Mixtures of hydrogel-forming absorbent polymers particles having this relatively high absorptive capacity characteristic are especially useful in the present invention since the resultant absorbent member formed from such particles can, by definition, hold desirably high amounts of fluid.
  • the absorbent structure may include some specialized materials developed to absorb oils and greases.
  • T-151 oil sorbent a 3M product, (Minnesota Mining and Manufacturing, ST. Paul, Minnesota)
  • T-151 absorbent and similar absorbent materials are typically non-woven polymeric fiber webs and include certain polyolefin polymers such as polypropylene, polyethylene, poly-4-methylpentene, arylene, styrene, and copolymers thereof, as well as polyesters, polyamides, and polycarbonates.
  • the Teabag Centrifuge Capacity test measures the Teabag Centrifuge Capacity values, which are a measure of the retention of liquids in the gelling material at hydrostatic pressure
  • the superabsorbent material is placed within a "teabag", immersed in a 0.9 % by weight sodium chloride solution for 20 minutes, and then centrifuged for 3 minutes.
  • the ratio of the retained liquid weight to the initial weight of the dry superabsorbent material is the absorptive capacity of the superabsorbent material.
  • the teabag pouch has dimensions 6.5cm x 6.5cm and is available from a company called Teekanne in D ⁇ sseldorf, Germany.
  • the pouch is heat sealable with a standard kitchen plastic bag sealing device (e.g. VACUPACK 2 PLUS from Krups, Germany) .
  • the teabag is opened by carefully cutting it partially, and is then weighed. A 0.200g +/- 0.005g sample of the superabsorbent material is placed in the teabag. The teabag is then closed with a heat sealer. This is called the sample teabag.
  • An empty teabag is sealed and used as a blank.
  • Each teabag is then held horizontally, and the sample teabag is shaken so as to distribute the superabsorbent material evenly throughout the bag.
  • the sample teabag and the blank teabag are then laid on the surface of the saline solution, and submerged for about 5 seconds using a spatular to allow complete wetting (the teabags will float on the surface of the saline solution but are completely wetted) .
  • the timer is started immediately.
  • the sample teabag and the blank teabag are removed from the salir.e solution, and placed in a Bauknecht WS130, Bosch 772 NZK096 or equivalent centrifuge (230 mm diameter) , so that each bag sticks to the outer wall of the centrifuge basket.
  • the centrifuge lid is closed, the centrifuge is started, and the speed increased quickly to l,400rpm. Once the centrifuge has been stabilised at l,400rpm the timer is started. After 3 minutes, the centrifuge is stopped.
  • the sample teabag and the blank teabag are removed and weighed separately.
  • TCC Teabag Centrifuge Capacity
  • TCC [ (sample teabag weight after centrifuging) - (blank teabag weight after centrifuging) - (dry superabsorbent hydrogel- forming material weight)] ⁇ (dry superabsorbent material weight) .
  • the particle size distribution of superabsorbent material is determined by placing a known weight of a sample in a Retsch mechanical sieving device, and shaking for a specified period of time under defined conditions. Sample sections that are retained on each sieve and the bottom pan are weighed and reported as percentages of the original sample weight. lOOg +/- 0.5g of dry superabsorbent polymeric material is weighed into a sample sup which is then closed by a lid.
  • the nested sieves are placed in position on a Retsch testing sieve shaker Vibotronic Type VEl with timer. It is ensured that the Retsch lid fits a s tightly as possible against the top of the shaker.
  • the timer is set for 10 minutes, and started to begin the test. When the shaker has stopped, the nest of sieves is removed from the shaker.
  • the mass median particle size of a given sample of hydrogel-forming absorbent polymer particles is defined as the particle size that divides the sample in half on a mass basis, i.e., one-half of the sample by weight will have a particle size less than the mass median size and one-half of the sample will have a particle size greater than the mass median size.
  • a standard particle- size plotting method (wherein the cumulative weight percent of the particle sample retained on or passed through a given sieve size opening is plotted versus sieve size opening on probability paper) is typically used to determine mass median particle size when the 50% mass value does not correspond to the size opening of a U.S.A. Standard Testing Sieve.
  • compositions are expressed as % by weight (unless otherwise stated) .
  • Shellsol ® is a mixture of C8-C11 isoparaffins with 5% aliphatic C7 ester.
  • Dehydol ® is a fatty alcohol polyglycol ether octyl 4EO, supplied by Henkel.
  • Dobanol " is a ethoxylated primary alcohol 3E0 supplied by Shell .
  • a set of polycotton swatches (50mm square) were soiled with make-up, chocolate sauce and tomato sauce. The stain was left to age for a day, in the dark, at normal room temperature (ca. 20°C, 60%RH) . Each soiled swatch was cleaned by the following method:
  • the stained area was placed directly upon a strip of absorbent paper (the paper used was the absorbent core of a diaper) .
  • Example 2 1 ml of the composition of Example 1 was dripped on to the stained area.
  • the stained area was brushed with a conventional electrical toothbrush for 10 seconds (the toothbrush used, a Braun dental d3, was one normally intended for daily oral care) .
  • Step 5. was repeated with a further 2ml of distilled water.
  • Cyclohexanol 7 6 5 isopropanol 2 2.5 toluene 20 20 15
  • Citric acid 5 5 16.1 3.57
  • MA/AA Acrylic maleic based copolymers, MW of 70000, the ratio of acrylate to maleate segments vary from 10:1 to 2:1. Sokalan CP5 from BASF
  • Kerosene 8.5 isoparaffinic hydrocarbon 6.2 pine oil 8.5
  • Example 79 A set of wool, polycotton and cotton swatches (50mm square) were soiled with honey, salad dressing and tomato sauce. The stain was left to age for a day, in the dark, at normal room temperature (ca. 20°C, 60%RH) . Each soiled swatch was cleaned by the following method.
  • the stained area was placed directly upon a strip of absorbent paper (the paper used was the absorbent core of a diaper) .
  • Example 74 1 ml of the composition of Example 74 was applied on to the stained area by means of an applicator of design indicated in fig 1.
  • This applicator comprised a bottle, a cap with a pad of polyurethane foam attached to it .
  • the cap has a small central opening through which the liquid can pass.
  • the stain was massaged with the outer surface of the pad to loosen it.
  • Step 3. was repeated with a further 2ml of distilled water.
  • the swatch was then dried and smoothed.
  • the method of cleaning was repeated on stained swatches using the applicator of figures 2 to 7 in place of the applicator of figure 1.
  • the method of cleaning was repeated 0:1 polycotton swatches stained with dirty motor oil using the applicator of figure 4 in place of the c.pplicator of figure 1 and the cleaning composition of example 5 in place of the composition of example 74.
  • a set of cotton swatches (50mm square) were soiled with lipstick and clay. The stain was left to age for a day, in the dark, at normal room temperature (ca. 20°C, 60%RH) . Each soiled swatch was cleaned by the following method.
  • the stained area was placed directly upon a strip of absorbent paper (the paper used was the absorbent core of a diaper) .
  • Example 6 1 ml of the composition of Example 6 was applied on to the stained area by means of an applicator of a design indicated in fig 7. After application of the detergent composition, the stain was massaged with the tip of the cleansing bottle to loosen it.
  • Example 80 3. 1 ml of the composition of Example 80 was sprayed on the stained area, and pressure and heat were applied using an iron set at a temperature of 100°C for 15 seconds. A typical ironing pressure, as no ⁇ rally used for removing wrinkles in fabrics, was used.
  • Step 3 was repeated with a further 2ml of distilled water.
  • Triton QS-30 1 0.5
  • MA/AA Acrylic maleic based copolymers, MW of 70000, the ratio of acrylate to maleate segments vary from 10:1 to 2:1. Sokalan CP5 from BASF
  • a set of silk and wool swatches (50mm square) were soiled with make-up and tomato sauce.
  • the stain was left to age for a day, in the dark, at normal rootr. temperature (ca. 20°C, 60%RH) .
  • Each soiled ⁇ watch was cleaned by the following method.
  • the stained area was placed directly upon a strip of absorbent paper (the paper used was the absorbent core of a diaper) .
  • a non-linting sheet is prepared using a ncn-woven, two-ply fabric stock comprising polyester fibres, calliper 0.25 to 0.34 mm, basis weight 84g/m 2 .
  • the fabric is cut into a 100cm 2 sheet, 10cm on a side.
  • 10 g of the composition of example 19 are applied by dipping the composition onto the substrate, followed by squeezing with a roller.
  • This sheet is placed on top of the soiled area.
  • the area of overlap between the paper and the soil is brushed with a toothbrush for 10 seconds.
  • a typical pressure as normally used to clean teeth was used. After brushing the paper is discarded.
  • Step 3. was repeated with a further 2ml of water.
  • the swatch was then dried and smoothed.
  • the soiled area was pretreated by pressing or rubbing with a sheet prepared according to the instructions given here above. After pretreatment with the cleaning sheet, the stained area was cleaned with the iron in the manner described in steps 3, 4 and 5 herein. In this mode of application, during the rubbing stage, the stain is pushed through the fabric onto the underlying absorbent paper.
  • a set of silk and wool swatches (50mm square) were soiled with make-up and tomato sauce.
  • the stain was left to age for a day, in the dark, at normal room temperature (ca. 20°C, 60%RH) .
  • Each soiled swatch was cleaned by the following method.
  • the stained area was placed directly upon a strip of absorbent paper (the paper used was a sheet of kitchen paper towel) .
  • a non-linting sheet is prepared using a non-woven, two-ply fabric stock comprising polyester fibres, calliper 0.25 to 0.34 mm, basis weight 84g/m 2 .
  • the fabric is cut into a 100cm 2 sheet, 10cm on a side.
  • 10 g of the composition of example 19 are applied by dipping the composition onto the substrate, followed by squeezing with a roller.
  • This sheet is placed on top of the soiled area.
  • the soiled area sandwiched between the paper towel and the cleaning sheet was inserted between the clips of the device of a design given in fig 8.
  • the body of the device is made of plastic, a pad of polyurethane foam is attached on each side of the clip. 54
  • the gap between the sponges is closed by applying pressure to the connecting means as indicated by the arrow, thereby causing the sponges to contact with the cleaning sheet and the paper towel.
  • the tool thus designed allows pushing of the stain through the fabric onto the underlying absorbent paper without any damage to the fabric.
  • Step 3. was repeated with a further 2ml of water.
  • the swatch was then dried and smoothed.
  • the method of cleaning was repeated on stained swatches using the spot cleaning device of Fig. 9 in place of the spot cleaning device of Fig. 8.
  • a set of polycotton swatches (50mm square) were soiled with make-up, chocolate sauce and tomato sauce. The stain was left to age for a day, in the dark, at normal room temperature (ca. 20°C, 60%RH) . Each so:.led swatch was cleaned by the following method:
  • the stained area was placed directly upon a strip of absorbent paper (the paper used was the absorbent core of a diaper) . 2. 1 ml of the composition of Example 1 was dripped on to the stained area.
  • the stained area was brushed with a dual-temperature cordless massager from Ultratherm , model TM2000.
  • Step 5. was repeated with a further 2ml of distilled water.
  • a set of polycotton swatches (50mm square) were soiled with make-up, chocolate sauce and tomato sauce. The stain was left to age for a day, in the dark, at normal room temperature (ca. 20°C, 60%RH) . Each soiled swatch was cleaned by the following method: 1. The stained area was placed directly upon a strip of absorbent paper (the paper used was the absorbent core of a diaper) .
  • composition of example 19 was dripped on to the stained area, and pressure and heat were applied using an iron (Braun" Saphir 7000) set at a temperature of 100°C for 10 seconds.
  • An ironing pressure as normally used for removing wrinkles in fabrics, was used.
  • Step 4. was repeated with a further 2ml of distilled water.
  • a set of silk and wool swatches (50mm square) were soiled with make-up, chocolate sauce and tomato sauce. The stain was left to age for a day, in the ark, at normal room temperature (ca. 20°C, 60%RH) . Each soiled swatch was cleaned by the following method:
  • the stained area was placed directly upon a strip of absorbent paper (the paper used was the absorbent core of a diaper) .
  • Example 19 The water tank of a Rowenta Steam Brush DA55 was filled with the composition of Example 19. The appliance was placed over the stained area, and 1 ml of the detergent composition was steamed on to it.
  • Step 5. was repeated with a further 2ml of distilled water.
  • a set of silk and wool swatches (50mm square) were soiled with make-up and tomato sauce.
  • the stain was left to age for a day, in the dark, at normal room temperature (ca. 20°C, 60%RH) .
  • Each soiled swatch was cleaned by the following method.
  • a non-linting sheet is prepared using a non-woven, two-ply fabric stock comprising polyester fibres, calliper 0.25 to 0.34 mm, basis weight 84g/m 2 .
  • the fabric is cut into a 100 cm 2 sheet, 10 cm on a side.
  • 10 g of the composition of example 19 are applied by dipping the composition onto the substrate, followed by squeezing with a roller.
  • a hand-held spot removal device as shown in Figure 10 is prepared using conventional plastic injection molding techniques and apparatus.
  • the arms which comprise the connecting means are fashioned from polypropylene, about (0.48 cm) in thickness.
  • the connecting mean ⁇ i may each have a uniform width of about (1.9 cm), or can be shaped to provide a more aesthetically pleasing aspect by gently narrowing the connecting means to a width of about (1.27cm) at the bend shown in the Figure.
  • the overall length of the device is about (13.34 cm) .
  • the diameter of the base of each treatment member is about (3.33 cm) and the diameter of the region of the looped protrusions extending outwardly from each treatment member is about (2.86 cm) .
  • the gap between the first and second treatment members is about (1.59 cm) when the device is at rest.
  • the gap is easily closed such that the protrusions which extend from each treatment members are brought into contact with opposite sides of the stains on the fabrics being treated.
  • the protrusions comprise stiff, looped monofilament fibers which extend from the face of each treatment member for a distance of about 2.0 mm.
  • the soiled area is moistened with cleaning composition by gently dabbing it with a sheet article of the foregoing type.
  • a device of the type shown in Figure 10 is placed at the stained area, with the treatment members on either side of the fabric area of staining.
  • the device is squeezed 10-30 times, slowly, to bring the illustrated looped protuberances into close contact with the fabric, thereby loosening the stain without damaging the fabric surface.
  • the area is then again padded with the sheet article.
  • the stained area was then placed directly upon a slip of absorbent paper (the paper used was a sheet of kitchen paper towel) .
  • Step 3 was repeated with a further 2 ml of water.
  • the method of cleaning was repeated on stained swatches using the spot cleaning device of Figure 8 to 9 in place of the spot cleaning device of Figure 10.

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PCT/US1996/019171 1995-11-27 1996-11-27 Cleaning method for textile fabrics WO1997020099A1 (en)

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BR9611771A BR9611771A (pt) 1995-11-27 1996-11-27 Método de limpeza para tecidos têxteis
DE69628464T DE69628464D1 (de) 1995-11-27 1996-11-27 Reinigungsverfahren für stoffe
US09/077,284 US6048368A (en) 1995-11-27 1996-11-27 Cleaning method for textile fabrics
AT96943549T ATE241691T1 (de) 1995-11-27 1996-11-27 Reinigungsverfahren für stoffe
AU12766/97A AU1276697A (en) 1995-11-27 1996-11-27 Cleaning method for textile fabrics
EP96943549A EP0910619B1 (en) 1995-11-27 1996-11-27 Cleaning method for textile fabrics
JP09520730A JP3093279B2 (ja) 1995-11-27 1996-11-27 編織布の洗浄法
NO982358A NO982358L (no) 1995-11-27 1998-05-25 FremgangsmÕte ved rensing av tekstilstoff

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EP95118617.0 1995-11-27
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WO1999004082A1 (en) * 1997-07-21 1999-01-28 The Procter & Gamble Company Fabric stain removal method
WO1999036611A1 (en) * 1998-01-16 1999-07-22 The Procter & Gamble Company Method for removing water spots from fabrics
WO2000078906A1 (en) * 1999-06-23 2000-12-28 Reckitt Benckiser Inc Spot cleaning compositions useful for cleaning garments and textiles
EP1069179A1 (en) * 1999-07-12 2001-01-17 The Procter & Gamble Company Stain removal method
WO2001004261A1 (en) * 1999-07-12 2001-01-18 The Procter & Gamble Company A method of stain removal from garments worn on the body
EP1123433A1 (en) * 1998-10-13 2001-08-16 Dry, Inc. Dry-cleaning article, composition and methods
WO2001079413A1 (en) * 2000-04-14 2001-10-25 Unilever Plc Process for spot removal
WO2001098449A1 (en) 2000-06-19 2001-12-27 The Procter & Gamble Company Bleach stabiliser for stain removal pen
WO2002079362A2 (en) * 2001-04-02 2002-10-10 Unilever N.V. Fabric cleaning
WO2002079368A1 (en) * 2001-04-02 2002-10-10 Unilever N.V. Fabric cleaning
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WO2002079363A2 (en) * 2001-04-02 2002-10-10 Unilever N.V. Cleaning device and its use
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EP1354937A1 (en) * 2002-04-18 2003-10-22 Illinois Tool Works Inc. Cleaning solvent and dispenser
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US6829913B2 (en) 2001-04-02 2004-12-14 Unilever Home & Personal Care Usa, A Division Of Conopco, Inc. Fabric cleaning
US6832867B2 (en) 1999-07-12 2004-12-21 The Procter & Gamble Company Fabric treatment applicator
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WO1999004082A1 (en) * 1997-07-21 1999-01-28 The Procter & Gamble Company Fabric stain removal method
WO1999036611A1 (en) * 1998-01-16 1999-07-22 The Procter & Gamble Company Method for removing water spots from fabrics
US7959686B2 (en) 1998-10-13 2011-06-14 Dry, Inc. Dry-cleaning article, composition and methods
US7744654B2 (en) 1998-10-13 2010-06-29 Dry, Inc. Dry-cleaning article, composition and methods
US6855172B2 (en) 1998-10-13 2005-02-15 Dry, Inc. Dry-cleaning article, composition and methods
US7300467B2 (en) 1998-10-13 2007-11-27 Dry, Inc. Dry-cleaning article, composition and methods
US7446083B2 (en) 1998-10-13 2008-11-04 Dry, Inc. Dry-cleaning article, composition and methods
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EP1123433A4 (en) * 1998-10-13 2002-06-12 Dry Inc DRY CLEANING ARTICLE, COMPOSITION AND METHODS
US8398721B2 (en) 1998-10-13 2013-03-19 Dry, Inc. Dry-cleaning article, composition and methods
WO2000078906A1 (en) * 1999-06-23 2000-12-28 Reckitt Benckiser Inc Spot cleaning compositions useful for cleaning garments and textiles
US6644879B2 (en) 1999-07-12 2003-11-11 The Procter & Gamble Company Stain removal pen with optimal application device
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WO2001004261A1 (en) * 1999-07-12 2001-01-18 The Procter & Gamble Company A method of stain removal from garments worn on the body
WO2001004259A1 (en) * 1999-07-12 2001-01-18 The Procter & Gamble Company Stain removal method
US6838423B2 (en) * 1999-07-12 2005-01-04 The Procter & Gamble Company Method of stain removal from garments worn on the body
US6832867B2 (en) 1999-07-12 2004-12-21 The Procter & Gamble Company Fabric treatment applicator
WO2001079413A1 (en) * 2000-04-14 2001-10-25 Unilever Plc Process for spot removal
US6846332B2 (en) 2000-06-19 2005-01-25 The Procter & Gamble Company Bleach stabilizer for stain removal pen
WO2001098449A1 (en) 2000-06-19 2001-12-27 The Procter & Gamble Company Bleach stabiliser for stain removal pen
US6883353B2 (en) 2001-04-02 2005-04-26 Unilever Home & Personal Care Usa Divison Of Conopco, Inc. Fabric cleaning
WO2002079367A1 (en) * 2001-04-02 2002-10-10 Unilever N.V. Fabric cleaner
WO2002079363A3 (en) * 2001-04-02 2002-11-28 Unilever Nv Cleaning device and its use
WO2002079363A2 (en) * 2001-04-02 2002-10-10 Unilever N.V. Cleaning device and its use
WO2002079362A3 (en) * 2001-04-02 2002-12-05 Unilever Nv Fabric cleaning
WO2002079370A1 (en) * 2001-04-02 2002-10-10 Unilever N.V. Fabric cleaning
WO2002079362A2 (en) * 2001-04-02 2002-10-10 Unilever N.V. Fabric cleaning
US6829913B2 (en) 2001-04-02 2004-12-14 Unilever Home & Personal Care Usa, A Division Of Conopco, Inc. Fabric cleaning
WO2002079369A1 (en) * 2001-04-02 2002-10-10 Unilever N.V. Fabric cleaning
WO2002079368A1 (en) * 2001-04-02 2002-10-10 Unilever N.V. Fabric cleaning
EP1327675A1 (en) * 2002-01-11 2003-07-16 Illinois Tool Works Inc. Cleaning solvent and dispenser
EP1354937A1 (en) * 2002-04-18 2003-10-22 Illinois Tool Works Inc. Cleaning solvent and dispenser
US7743443B2 (en) 2006-06-19 2010-06-29 S.C. Johnson & Son, Inc. Liquid applicator and absorbent scrubbing means
US7832041B2 (en) 2006-06-19 2010-11-16 S.C. Johnson & Son, Inc. Instant stain removing device, formulation and absorbent means
EP2202290A1 (en) * 2008-12-23 2010-06-30 Unilever PLC A flowable laundry composition and packaging therefor
WO2010072529A1 (en) * 2008-12-23 2010-07-01 Unilever Plc A flowable laundry composition and packaging therefor

Also Published As

Publication number Publication date
NO982358L (no) 1998-06-22
CA2238497A1 (en) 1997-06-05
NO982358D0 (no) 1998-05-25
EP0910619B1 (en) 2003-05-28
EP0910619A4 (da) 1999-04-28
DE69628464D1 (de) 2003-07-03
EP0910619A1 (en) 1999-04-28
JPH11506174A (ja) 1999-06-02
JP3093279B2 (ja) 2000-10-03

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