EP2922936A1 - Compositions de lessive - Google Patents

Compositions de lessive

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Publication number
EP2922936A1
EP2922936A1 EP13771155.2A EP13771155A EP2922936A1 EP 2922936 A1 EP2922936 A1 EP 2922936A1 EP 13771155 A EP13771155 A EP 13771155A EP 2922936 A1 EP2922936 A1 EP 2922936A1
Authority
EP
European Patent Office
Prior art keywords
silicone
polymer
cationic
composition according
composition
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
EP13771155.2A
Other languages
German (de)
English (en)
Other versions
EP2922936B1 (fr
Inventor
Andrew Anthony Howard Barnes
Neil Stephen Burnham
Martin Charles Crossman
Belinda Fay DAWSON
Paula Rose Bernadette GILFOYLE
Jane Catherine JONES
Atsuko KAWABATA
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 Global IP Ltd
Unilever IP Holdings BV
Original Assignee
Unilever PLC
Unilever NV
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Application filed by Unilever PLC, Unilever NV filed Critical Unilever PLC
Priority to EP13771155.2A priority Critical patent/EP2922936B1/fr
Publication of EP2922936A1 publication Critical patent/EP2922936A1/fr
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Classifications

    • 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
    • C11D1/008—Polymeric surface-active agents
    • 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
    • C11D3/0005—Other compounding ingredients characterised by their effect
    • C11D3/001—Softening 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
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/20—Organic compounds containing oxygen
    • C11D3/22—Carbohydrates or derivatives thereof
    • C11D3/222—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
    • C11D3/227—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin with nitrogen-containing groups
    • 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
    • C11D3/16—Organic compounds
    • C11D3/37—Polymers
    • C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/373—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones

Definitions

  • This invention relates to a laundry composition. More particularly, the invention is directed to a softening in the wash laundry composition.
  • Fabric softening cationic polymers, and fabric softening silicones have been used to provide softness to fabrics from a laundry detergent composition.
  • WO 2005/087907 discloses liquid detergent compositions comprising surfactants, polydimethylsiloxane (a softening silicone) and polyquaternium 7 (a polymeric quaternary salt consisting of acrylamide and dimethyl diallyl ammonium chloride monomers).
  • the invention is directed to a laundry detergent composition
  • a laundry detergent composition comprising:-
  • weight ratio of the silicone to cationic polysaccharide polymer is from 4.5:1 to 1 .5:1 .
  • the detergent composition is a liquid detergent composition.
  • the liquid detergent composition has a pH of from 6 to 10, more preferably from pH 6.5 to 9, for example from pH 6.5 to 8.5.
  • a preferred level of the cationic polymer is from 0.1 to 2 wt.%, more preferably from 0.1 to 1 wt.%.
  • Preferred cationic polysaccharide polymers are cationic guar and cationic cellulose polymers. Particularly preferred is hydroxy ether cellulose that is modified by incorporation of cationic groups (i.e. quaternised hydroxy ethyl cellulose).
  • the silicone is in the form of an emulsion.
  • the silicone is a polydimethylsiloxane.
  • the silicone is an aminosilicone.
  • the silicone is an anionic silicone.
  • the weight ratio of the silicone to the cationic polymer is from 4:1 to 2:1 .
  • the composition further comprises an ingredient selected from, shading dye, enzyme, an antiredeposition polymer, a dye transfer inhibiting polymer, builder, sequestrant, sunscreen and/or soil release polymer.
  • the invention provides the use of a composition according to the first aspect of the invention to soften fabrics. DETAILED DESCRIPTION OF THE INVENTION
  • the term “comprising” means including, made up of, composed of, consisting and/or consisting essentially of.
  • the invention is directed to laundry compositions containing surfactant, a cationic polymer, and a fabric softening silicone, wherein the weight ratio of silicone to cationic polymer is from 4.5:1 to 1 .5:1 .
  • the composition displays improved fabric softening.
  • the invention can take any of a number of forms that are laundry compositions. Examples include powders, granules, bars, gels and liquids. Preferably the composition is in the form of a liquid laundry product. Preferably they are main wash products. It can take the form of a laundry composition for the main wash, which may be dilutable or non-dilutable.
  • the laundry composition may for example be an isotropic liquid, or a surfactant-structured liquid.
  • Particularly preferred forms of this invention include combination detergent/softener products to provide "softening in the wash".
  • the detergent composition has a pH of from 6 to 10, more preferably from pH 6.5 to 9, for example from pH 6.5 to 8.5.
  • the detergent composition comprises surfactant.
  • the surfactant comprises nonionic surfactant, and anionic surfactant.
  • the nonionic surfactant if present, preferably comprises alcohol ethoxylate.
  • the alcohol ethoxylates are formed from the reaction of primary or secondary alcohols with ethylene oxide.
  • ethylene oxide is reacted with ethylene oxide in the required molar amount to produce the alcohol ethoxylate.
  • Preferred alcohol ethoxylates have from 2 to 40, preferably from 3 to 30, more preferably from 5 to 20 ethylene oxide units attached to the aliphatic chain.
  • the surfactants may be chosen from the surfactants described in "Surface Active Agents” Vol. 1 , by Schwartz & Perry, Interscience 1949, Vol. 2 by Schwartz, Perry & Berch, Interscience 1958, in the current edition of "McCutcheon's Emulsifiers and Detergents” published by Manufacturing Confectioners Company or in "Tenside-Taschenbuch", H. Stache, 2nd Edn., Carl Hauser Verlag, 1981 .
  • the surfactants used are saturated.
  • Suitable nonionic detergent compounds which may be used include, in particular, the reaction products of compounds having a hydrophobic group and a reactive hydrogen atom, for example, aliphatic alcohols, acids, amides or alkyl phenols with alkylene oxides, especially ethylene oxide either alone or with propylene oxide.
  • Specific nonionic detergent compounds are C 6 to C 2 2 alkyl phenol- ethylene oxide condensates, generally 5 to 25 EO, i.e. 5 to 25 units of ethylene oxide per molecule, and the condensation products of aliphatic Cs to C-is primary or secondary linear or branched alcohols with ethylene oxide, generally 5 to 40 EO.
  • Suitable anionic detergent compounds which may be used can be water-soluble alkali metal salts of organic sulphates and sulphonates having alkyl radicals con- taining from about 8 to about 22 carbon atoms, the term alkyl being used to include the alkyl portion of higher acyl radicals.
  • suitable synthetic anionic detergent compounds are sodium and potassium alkyl sulphates, especially those obtained by sulphating higher Cs to Cie alcohols, produced for example from tallow or coconut oil, sodium and potassium alkyl Cg to C20 benzene sulphonates, particularly sodium linear secondary alkyl C-m to C15 benzene sulphonates; and sodium alkyl glyceryl ether sulphates, especially those ethers of the higher alcohols derived from tallow or coconut oil and synthetic alcohols derived from petroleum.
  • the anionic surfactant may also include soaps of C6-C22 fatty acids.
  • the preferred anionic detergent compounds are sodium Cn to C-I5 alkyl benzene sulphonates and sodium C12 to Ci 8 alkyl sulphates. Salts of sulphonates included as hydrotrobes can additionally be considered as anionic surfactants as defined herein. Also applicable are surfactants such as those described in EP-A-328 177 (Unilever), which show resistance to salting-out, the alkyl polyglycoside surfactants described in EP-A-070 074, and alkyl
  • the total amount of surfactant present in the composition is from 1 to 80 wt.%.
  • the surfactant level is preferably at least 6 wt.%, more preferably at least 10 wt.%, More preferably the total amount of surfactant is from 15 to 65 wt.%, preferably from 10 to 50 wt.%.
  • the nonionic detergent is preferably present in amounts of from 2 to 40 wt.%, preferably from 5 to 35 wt.%, more preferably from 6 to 20 wt.%.
  • the anionic surfactant is preferably present in amounts of from 4 to 40 wt.%, preferably from 5 to 35 wt.%, more preferably from 6 to 20 wt.%.
  • surfactants such as amphoteric, zwitterionic and cationic surfactants may also be present in addition to the aforementioned nonionic and anionic
  • the composition comprises fabric softening silicone at a level of from 0.1 to 10 wt.%, preferably from 0.2 to 5 wt.%, more preferably from 0.5 to 3 wt.%.
  • the fabric softening silicone may be but are not limited to 1 ) non-functionalized silicones such as polydimethylsiloxane (PDMS) or alkyl (or alkoxy) functional silicones 2) functionalized silicones or copolymers with one or more different types of functional groups such as amino, phenyl, polyether, acrylate, siliconhydride, carboxylic acid, quaternized nitrogen, etc.
  • the particle size is in the range from about 1 nm to 100 microns and preferably from about 10 nm to about 10 microns including microemulsions ( ⁇ 150 nm), standard emulsions (about 200 nm to about 500 nm) and macroemulsions (about 1 micron to about 20 microns).
  • Preferred silicones are selected from polydialkylsiloxanes, especially
  • polydimethylsiloxane polydimethylsiloxane; amino functionalised silicones; and anionic silicones, especially carboxyl functionalised silicone
  • the fabric softening silicone is a polydimethylsiloxane.
  • the composition comprises a cationic polysaccharide polymer at a level of from 0.05 to 2.5 wt.%, preferably from 0.1 to 2 wt.%, more preferably from 0.2 to 1 wt.%.
  • This term refers to polymers having an overall positive charge.
  • the cationic polysaccharide polymer is a cationic guar or cationic cellulose polymer. Most preferably the cationic polymer is a cationic cellulose polymer, for example, quaternised hydroxy ethyl cellulose. Cationic Polysaccharide Polymer
  • cationic polysaccharide polymer refers to polymers having a
  • Polysaccharide backbone and an overall positive charge Polysaccharides are polymers made up from monosaccharide monomers joined together by glycosidic bonds.
  • the cationic polysaccharide-based polymers present in the compositions of the invention have a modified polysaccharide backbone, modified in that additional chemical groups have been reacted with some of the free hydroxyl groups of the polysaccharide backbone to give an overall positive charge to the modified cellulosic monomer unit.
  • a preferred class of cationic polysaccharide polymers suitable for this invention are those that have a polysaccharide backbone modified to incorporate a quaternary ammonium salt.
  • the quaternary ammonium salt is linked to the polysaccharide backbone by a hydroxyethyl or hydroxypropyl group.
  • the charged nitrogen of the quaternary ammonium salt has one or more alkyl group substituents.
  • Preferred cationic polysaccharide-based polymers have a guar based, or cellulosic based backbone. Cellulose based cationic polymers are most preferred. Guar is a galactomannan having a ⁇ -1 ,4 linked mannose backbone with
  • Suitable cationic guar gum derivatives such as guar hydroxypropyltrimonium chloride, specific examples of which include the Jaguar series commercially available from Rhone-Poulenc Incorporated and the N-Hance series commercially available from Aqualon Division of Hercules, Inc.
  • An example of a preferred guar based cationic polymer is guar 2-hydroxy-3- (trimethylammonium) propyl ether salt.
  • Cellulose is a polysaccharide with glucose as its monomer, specifically it is a straight chain polymer of D-glucopyranose units linked via ⁇ -1 ,4 glycosidic bonds and is a linear, non-branched polymer.
  • Example cationic cellulose polymers are salts of hydroxyethyl cellulose reacted with trimethyl ammonium substituted epoxide, referred to in the field under the International Nomenclature for Cosmetic Ingredients as Polyquatemium 10 and is commercially available from the Amerchol Corporation, a subsidiary of The Dow Chemical Company, marketed as the Polymer LR, JR, and KG series of polymers.
  • Other suitable types of cationic celluloses include the polymeric quaternary ammonium salts of hydroxyethyl cellulose reacted with lauryl dimethyl ammonium- substituted epoxide referred to in the field under the International Nomenclature for Cosmetic Ingredients as Polyquatemium 24. These materials are available from Amerchol Corporation marketed as Polymer LM-200.
  • Typical examples of preferred cationic cellulosic polymers include
  • the cationic cellulosic polymer is a quaternised hydroxy ether cellulose cationic polymer. These are commonly known as polyquaternium-10. Suitable commercial cationic cellulosic polymer products for use according to the present invention are marketed by the Amerchol Corporation under the trade name UCARE.
  • the counterion of the cationic polymer is freely chosen from the halides: chloride, bromide, and iodide; or from hydroxide, phosphate, sulphate, hydrosulphate, ethyl sulphate, methyl sulphate, formate, and acetate.
  • the aforementioned cationic polymers can be synthesised in, and are commercially available in, a number of different molecular weights.
  • the molecular weight of the cationic polymer is from 10,000 to 2,000,000 Daltons, more preferably from 10,000 to 1 ,000,000 Daltons, even more preferably from 100,000 to 1 ,000,000 Daltons.
  • the detergent composition may optionally comprise one or more of the following optional ingredients, shading dye, enzyme, antiredeposition polymer, dye transfer inhibiting polymer, builder, sequestrant, sunscreen and/or soil release polymer.
  • the detergent compositions may also optionally contain relatively low levels of organic detergent builder or sequestrant material.
  • organic detergent builder or sequestrant material examples include the alkali metal, citrates, succinates, malonates, carboxymethyl succinates, carboxylates, polycarboxylates and polyacetyl carboxylates.
  • specific examples include sodium, potassium and lithium salts of oxydisuccinic acid, mellitic acid, benzene
  • polycarboxylic acids ethylene diamine tetra-acetic acid, diethylenetriamine- pentaacetic acid, alkyl- or alkenylsuccinic acid, nitrilotriacetic acid, and citric acid.
  • DEQUESTTM organic phosphonate type sequestering agents sold by Thermophos and alkanehydroxy phosphonates.
  • suitable organic builders include the higher molecular weight polymers and copolymers known to have builder properties.
  • such materials include appropriate polyacrylic acid, polymaleic acid, and polyacrylic/polymaleic acid copolymers and their salts, such as those sold by BASF under the name SOKALANTM.
  • Another suitable builder is sodium carbonate.
  • the builder materials may comprise from about 0.5% to 20 wt%, preferably from 1 wt% to 10 wt%, of the composition. The preferred builder level is less than 10 wt% and preferably less than 5 wt% of the composition.
  • the laundry detergent formulation is a non-phosphate built laundry detergent formulation, i.e., contains less than 1 wt.% of phosphate.
  • Shading dyes deposit to fabric during the wash or rinse step of the washing process providing a visible hue to the fabric. Shading of white garments may be done with any colour depending on consumer preference. Blue and Violet are particularly preferred shades and consequently preferred dyes or mixtures of dyes are ones that give a blue or violet shade on white fabrics. The shading dyes used are preferably blue or violet.
  • the shading dye chromophore is preferably selected from the group comprising: mono-azo, bis-azo, triphenylmethane, triphenodioxazine, phthalocyanin, naptholactam, azine and anthraquinone. Most preferably mono-azo, bis-azo, azine and anthraquinone.
  • the dye bears at least one sulfonate group.
  • Preferred shading dyes are selected from direct dyes, acid dyes, hydrophobic dyes, cationic dyes and reactive dyes.
  • the shading dye is present is present in the composition in range from 0.0001 to 0.01 wt %.
  • the composition preferably comprises a fluorescent agent (optical brightener).
  • fluorescent agents are well known and many such fluorescent agents are available commercially. Usually, these fluorescent agents are supplied and used in the form of their alkali metal salts, for example, the sodium salts.
  • the total amount of the fluorescent agent or agents used in the composition is generally from 0.005 to 2 wt.%, more preferably 0.01 to 0.1 wt.%.
  • Preferred classes of fluorescer are: Di-styryl biphenyl compounds, e.g. Tinopal (Trade Mark) CBS-X, Di-amine stilbene di-sulphonic acid compounds, e.g.
  • Preferred fluorescers are: sodium 2-(4-styryl-3-sulfophenyl)-2H-napthol[1 ,2- d]trazole, disodium 4,4'-bis ⁇ [(4-anilino-6-(N methyl-N-2 hydroxyethyl) amino 1 ,3,5- triazin-2-yl)]amino ⁇ stilbene-2-2' disulfonate, disodium 4,4'-bis ⁇ [(4-anilino-6- morpholino-1 ,3,5-triazin-2-yl)]amino ⁇ stilbene-2-2' disulfonate, and disodium 4,4'- bis(2-sulfoslyryl)biphenyl.
  • the composition comprises a perfume.
  • the perfume is preferably in the range from 0.001 to 3 wt.%, most preferably 0.1 to 1 wt.%.
  • CTFA Cosmetic, Toiletry and
  • compositions of the present invention it is envisaged that there will be four or more, preferably five or more, more preferably six or more or even seven or more different perfume components.
  • top notes are defined by Poucher (Journal of the Society of Cosmetic Chemists 6(2):80 [1955]).
  • Preferred top-notes are selected from citrus oils, linalool, linalyl acetate, lavender, dihydromyrcenol, rose oxide and cis-3-hexanol.
  • the laundry treatment composition does not contain a peroxygen bleach, e.g., sodium percarbonate, sodium perborate, and peracid.
  • a peroxygen bleach e.g., sodium percarbonate, sodium perborate, and peracid.
  • the composition may comprise one or more polymers.
  • Polymers can assist in the cleaning process by helping to retail soil in solution or suspension and/or preventing the transfer of dyes. Polymers can also assist in the soil removal process. Dye transfer, anti-redeposition and soil-release polymers are described in further detail below.
  • the composition may comprise one or more polymers. Examples are:
  • carboxymethylcellulose hydroxyethyl cellulose, hydroxpropyl cellulose, poly(ethylene glycol), polyvinyl alcohol), ethoxylated polyamines,
  • polycarboxylates such as polyacrylates, maleic/acrylic acid copolymers and lauryl methacrylate/acrylic acid copolymers.
  • Modern detergent compositions typically employ polymers as so-called 'dye- transfer inhibitors'. These prevent migration of dyes, especially during long soak times.
  • dye-transfer inhibiting agents include polyvinyl pyrrolidone polymers, polyamine N-oxide polymers, copolymers of N-vinylpyrrolidone and N- vinylimidazole, manganese pthalocyanine, peroxidases, and mixtures thereof, and are usually present at a level of from 0.01 to 10 wt.% based on total amount in the laundry composition.
  • Anti-redeposition polymers are designed to suspend or disperse soil.
  • antiredeposition polymers are ethoxylated and or propoxylated polyethylene imine or polycarboxylate materials, for example, Acrylic acid based homo or copolymers available under the trade mark ACUSOL from Dow Chemical, Alcosperse from Akzonobel or Sokolan from BASF. Soil Release Polymers
  • suitable soil release polymers include graft copolymers of polyvinyl ester), e.g., Ci -C 6 vinyl esters, preferably polyvinyl acetate) grafted onto polyalkylene oxide backbones.
  • Commercially available soil release agents of this kind include the SOKALAN type of material, e.g., SOKALAN HP-22, available from BASF (Germany).
  • Further suitable soil release polymers of a different type include the commercially available material ZELCON 5126 (from DuPont) and MILEASE T (from ICI). If present, the soil release polymer may be included at a level of from from 0.01 to 10 wt.% based on total amount in the laundry
  • soil release polymers are terephthalic acid / glycol copolymers sold under the tradenames Texcare, Repel-o-tex, Gerol, Marloquest, Cirrasol.
  • the liquid detergent composition may optionally include a hydrotrope, which can prevent liquid crystal formation.
  • a hydrotrope which can prevent liquid crystal formation.
  • the addition of the hydrotrope thus aids the clarity/transparency of the composition.
  • Suitable hydrotropes include but are not limited to propylene glycol, ethanol, glycerol, urea, salts of benzene sulphonate, toluene sulphonate, xylene sulphonate or cumene sulphonate.
  • Suitable salts include but are not limited to sodium, potassium, ammonium, monoethanolamine, triethanolamine. Salts of sulphonates can also be considered as anionic surfactants as defined herein.
  • the hydrotropes include but are not limited to propylene glycol, ethanol, glycerol, urea, salts of benzene sulphonate, toluene sulphonate, xylene sulphonate or cumene
  • hydrotrope is selected from the group consisting of propylene glycol, xylene sulfonate, ethanol, and urea to provide optimum performance.
  • the amount of the hydrotrope is generally in the range of from 0 to 30%, preferably from 0.5 to 30%, more preferably from 0.5 to 30%, most preferably from 1 to 15%.
  • Enzymes can also be present in the formulation.
  • Preferred enzymes include protease, lipase, pectate lyase, amylase, cutinase, cellulase, mannanase. If present the enzymes may be stabilized with a known enzyme stabilizer for example boric acid.
  • Silicone was a carboxylic functional silicone supplied by Wacker Chemie, added as an emulsion.
  • LR400 is a cationic hydroxyether cellulose polymer (known as polyquaternium 10) available from Dow Chemical
  • Silicone was a carboxylic functional silicone supplied by Wacker Chemie
  • 2 LR400 is a cationic hydroxyether cellulose polymer (known as polyquaternium 10) available from Dow Chemical
  • the softness was measured using a Stable Micro Systems Texture Analyser (TA) XT plus with the optional friction module attached.
  • the TA is a commercial instrument incorporating a drive mechanism and a 5 kg load cell.
  • the treated fabric was laid on the horizontal test platform of the instrument and a neoprene rubber cylindrical probe which is attached to the load cell was placed on the fabric surface.
  • the texture analyser is programmed to move the probe over a distance of 40 mm forwards and backwards over the fabric at a speed of 10 mm/s. As the probe moves the software records the frictional force experienced by the probe. The average friction coefficient over the whole test is used as a measure of softness.
  • Example 2 Further softness experiments were as performed to establish whether the effect of silicone to cationic polymer ratio is consistent across other functional silicones. In this case a PDMS and an amino silicone were used, and the results are shown in tables 4 & 5.
  • Silicone 1 was PDMS 60,000 cSt supplied by Dow Corning as an emulsion
  • Silicone 2 was amino silicone Arristan 64 supplied by CHT Beitlich as an emulsion 3 LR400 is a cationic hydroxyether cellulose polymer (known as polyquaternium 10) available from Dow Chemical Table 5
  • polyquaternium 7 from WO 2005/087907
  • Silicone deposition of both cationic polymers was tested using identical formulations varying only by the cationic polymer used. The formulations were dosed to provide silicone at 0.5g/wash and cationic polymer at 0.2g/wash. The variables tested were:-
  • Control - formulation including 0.5g/wash silicone
  • Polysaccharide - formulation including 0.5g/wash silicone + 0.2g/wash cationic polysaccharide polymer (LR400)
  • Polyquat 7 - formulation including 0.5g/wash silicone + 0.2g/wash cationic polymer (polyquaternium 7)
  • the washes were carried out on 2 different substrates, terry towelling; and repeated on white knitted cotton.
  • the articles were washed 6 times, dried and then friction measured after each wash. The friction measurement results in a average friction coefficient.
  • the friction test shows how soft the articles washed were, in that the amount of silicone deposited builds-up onto the article and decreases friction.
  • the coefficient of friction was measured using a commercially available Stable Micro Systems Texture Analyser.
  • the fabric article is placed onto a platform and a rubber probe placed on the fabric and moved at 10mm/s.
  • the probe is moved 40mm forwards, followed by 40mm backwards.
  • the instrument records the frictional force which is then converted into an average friction coefficient throughout the movement in both directions.
  • the data points in the following tables show that the polysaccharide provides statistically significant improvement in reduced friction (hence increased silicone deposition) at 95% confidence levels.
  • polysaccharide polymer provides superior deposition of silicone over that prior art polyquaternium-7 disclosed in WO 2005/087907.

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

Abstract

L'invention concerne des compositions de lessive contenant a) un tensioactif, b) un polymère polysaccharide cationique, et c) un silicone d'adoucissement de tissu, le rapport pondéral entre le silicone et le polymère polysaccharide cationique étatnt compris entre 4,5 : 1 et 1,5 : 1.
EP13771155.2A 2012-11-20 2013-10-02 Compositions de lavage Active EP2922936B1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP13771155.2A EP2922936B1 (fr) 2012-11-20 2013-10-02 Compositions de lavage

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP12193352 2012-11-20
EP13771155.2A EP2922936B1 (fr) 2012-11-20 2013-10-02 Compositions de lavage
PCT/EP2013/070526 WO2014079621A1 (fr) 2012-11-20 2013-10-02 Compositions de lessive

Publications (2)

Publication Number Publication Date
EP2922936A1 true EP2922936A1 (fr) 2015-09-30
EP2922936B1 EP2922936B1 (fr) 2019-08-14

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Family Applications (1)

Application Number Title Priority Date Filing Date
EP13771155.2A Active EP2922936B1 (fr) 2012-11-20 2013-10-02 Compositions de lavage

Country Status (7)

Country Link
EP (1) EP2922936B1 (fr)
CN (1) CN104781381B (fr)
AR (1) AR093522A1 (fr)
BR (1) BR112015008917B1 (fr)
CL (1) CL2015001055A1 (fr)
WO (1) WO2014079621A1 (fr)
ZA (1) ZA201502942B (fr)

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WO2021194808A1 (fr) * 2020-03-24 2021-09-30 Rohm And Haas Company Composition de soin des tissus

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WO2016077207A1 (fr) 2014-11-11 2016-05-19 Rohm And Haas Company Polymères glucidiques cationiques pour l'entretien des textiles
US10633613B2 (en) 2014-11-17 2020-04-28 Conopco, Inc. Fabric treatment composition comprising peg and an anionic and/or cationic silicone
CA2967514C (fr) 2014-11-17 2023-03-14 Unilever Plc Composition de traitement de textile
WO2017102874A1 (fr) 2015-12-18 2017-06-22 Henkel Ag & Co. Kgaa Composition de détergent liquide
CN109312523B (zh) 2016-06-09 2021-03-16 荷兰联合利华有限公司 洗衣液混合设备
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BR112015008917B1 (pt) 2022-02-01
WO2014079621A1 (fr) 2014-05-30
CN104781381B (zh) 2018-02-23
AR093522A1 (es) 2015-06-10
BR112015008917A2 (pt) 2017-07-04
CL2015001055A1 (es) 2015-08-28
ZA201502942B (en) 2016-09-28
EP2922936B1 (fr) 2019-08-14

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