[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

EP2366008B1 - Laundry compositions - Google Patents

Laundry compositions Download PDF

Info

Publication number
EP2366008B1
EP2366008B1 EP09771385A EP09771385A EP2366008B1 EP 2366008 B1 EP2366008 B1 EP 2366008B1 EP 09771385 A EP09771385 A EP 09771385A EP 09771385 A EP09771385 A EP 09771385A EP 2366008 B1 EP2366008 B1 EP 2366008B1
Authority
EP
European Patent Office
Prior art keywords
surfactant
composition
cationic
level
present
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.)
Active
Application number
EP09771385A
Other languages
German (de)
French (fr)
Other versions
EP2366008A1 (en
Inventor
Gillian Elaine Bullen
Bernard Jean-Denis
Dawn Rigby
Graham Philip Sale
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Unilever PLC
Unilever NV
Original Assignee
Unilever PLC
Unilever NV
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Unilever PLC, Unilever NV filed Critical Unilever PLC
Priority to EP09771385A priority Critical patent/EP2366008B1/en
Publication of EP2366008A1 publication Critical patent/EP2366008A1/en
Application granted granted Critical
Publication of EP2366008B1 publication Critical patent/EP2366008B1/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/001Softening compositions
    • C11D3/0015Softening compositions liquid
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D10/00Compositions of detergents, not provided for by one single preceding group
    • C11D10/04Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/22Carbohydrates or derivatives thereof
    • C11D3/222Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
    • C11D3/227Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin with nitrogen-containing groups
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds

Definitions

  • This invention relates to a laundry composition. More particularly, the invention is directed to a softening in the wash laundry composition.
  • One such softening system comprises a cationic polysaccharide and anionic surfactant.
  • a cationic polysaccharide and anionic surfactant.
  • Such systems are known from WO 2004/069979 which discloses particular combinations of cationic polymers and anionic surfactants.
  • WO 2008/022838 discloses liquid laundry compositions comprising anionic surfactant, nonionic surfactant, fatty acid and cationic polymers. The compositions are stated to provide both effective softening and cleaning.
  • WO2007/107215 A1 discloses a process for the preparation of a non-aqueous fabric treatment composition comprising a) provision of a pre-mix comprising cationic cellulose polymer, water and optional solvent; b) admixture of the pre-mix with anionic surfactant; and c) subsequent addition of non-ionic surfactant.
  • WO 2008/114171 A1 discloses a liquid laundry detergent comprising anionic surfactant, fabric core agent, cationic deposition aid and performance booster.
  • this invention is directed to a liquid detergent composition
  • a liquid detergent composition comprising:-
  • this invention is directed to a method for the provision of softness to a textile, comprising the steps:
  • the term “comprising” means including, made up of, composed of, consisting and/or consisting essentially of.
  • a formula shall be considered physically "stable" when after 1 week at 21 degrees Celsius it exhibits no signs of phase separation.
  • the present invention is directed to laundry compositions containing fatty acid or salt thereof, a polysaccharide-based cationic polymer, a non-ionic surfactant and an anionic surfactant, wherein the ratio of nonionic to anionic surfactant is from 1.25:1 to 2.25:1, and wherein the total level of surfactant is at least 25 wt.% and in accordance with claim 1.
  • the composition delivers a high level of softening to fabrics in comparison to the prior art.
  • the composition also displays excellent stability.
  • Softening includes, but is not limited to, an improvement in the handling of a garment treated with the compositions of this invention relative to that of an article laundered under identical conditions but without the use of this invention. Consumers will often describe an article that is softened as “silky” or “fluffy”, and generally prefer the feel of treated garments to those that are unsoftened.
  • compositions of these compositions are not limited to just softening, however. They may, depending on the particular embodiment of the invention selected, also provide an antistatic benefit.
  • the cationic polymer/anionic surfactant compositions of this invention are further believed to lubricate the fibres of textile articles, which can reduce wear, pilling and colour fading, and provide a shape-retention benefit. This lubricating layer is also believed to provide a substrate on the fabric for retaining fragrances and other benefit agents.
  • the present invention can take any of a number of forms that are included as main wash products. It can take the form of a laundry treatment agent for the main wash, which may be dilutable or non-dilutable.
  • the laundry treatment agent 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".
  • softening in the wash is meant a composition which provides a fabric softening benefit as well as providing cleaning to the laundered fabric.
  • a composition can be added as part of a main wash product, or as a separate product for use in combination with another.
  • the composition is intended for use in the main wash cycle.
  • the softening in the wash composition of the invention is incorporated as part of a single product for use in the main wash.
  • the pH range of the composition is 7-12, preferably 8.5 to 9.5. It is desirable to buffer the formulation at whatever the target pH of the composition is.
  • the liquid detergent composition provides a softness benefit to the laundered fabrics by a method comprising the steps:
  • the liquid detergent compositions include fatty acid or salt thereof, a term used herein interchangeably with the term 'soap'. Both terms are herein defined as an alkali or alkaline earth metal salt of a natural or synthetic fatty acid containing between 6 and 30 carbon atoms.
  • the soap contains between C 8 -C 26 , more preferably C 8 -C 24 , still more preferably C 8 -C 18 carbon atoms.
  • the incorporation level of the soap is from 2 to 14%, preferably from 2.5 to 10%, more preferably from 3 to 9% by weight of the total composition. Particularly preferred forms of soap are outlined below.
  • R 1 COOM where R 1 is a primary or secondary alkyl group of 5 to 29 carbon atoms and M is a solubilising cation.
  • the alkyl group represented by R 1 may represent a mixture of chain lengths and may be saturated or unsaturated, although it is preferred that at least two thirds of the R 1 groups have a chain length of between 7 and 17 carbon atoms.
  • suitable alkyl group sources include the fatty acids derived from coconut oil, tallow, tall oil and palm kernel oil. For the purposes of minimising odour, however, it is often desirable to use primarily saturated carboxylic acids.
  • the solubilising cation, M is an alkali or alkaline earth metal cation.
  • Preferred examples of cations include alkali metals such as sodium and potassium.
  • the liquid detergent composition comprises nonionic surfactant, and anionic surfactant other than soap.
  • the soap present in the composition is not included in the calculation of anionic surfactant for weight inclusion or weight ratios present in the composition.
  • the wt.% of soap present is not included the total amount of surfactant present.
  • 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 22 alkyl phenolethylene oxide condensates, generally 5 to 25 EO, i.e. 5 to 25 units of ethylene oxide per molecule, and the condensation products of aliphatic C 8 to C 18 primary or secondary linear or branched alcohols with ethylene oxide, generally 5 to 40 EO.
  • Suitable anionic detergent compounds which may be used are usually watersoluble alkali metal salts of organic sulphates and sulphonates having alkyl radicals containing 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 C 8 to C 18 alcohols, produced for example from tallow or coconut oil, sodium and potassium alkyl C 9 to C 20 benzene sulphonates, particularly sodium linear secondary alkyl C 10 to C 15 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 preferred anionic detergent compounds are sodium C 11 to C 15 alkyl benzene sulphonates and sodium C 12 to C 18 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 monoglycosides.
  • the nonionic detergent is present in amounts of from 6 to 40 wt.%, preferably from 7.5 to 35 wt.%, more preferably from 10 to 25 wt.%.
  • the anionic surfactant is present in amounts of from 6 to 20 wt.%, preferably from 6.5 to 17.5 wt.%, more preferably from 7.5 to 15 wt.%.
  • the ratio of nonionic surfactant to anionic surfactant present in the liquid composition is from 1.25:1 to 2.25:1, based on weight.
  • the total amount of surfactant present in the liquid composition is at least 25 wt.%.
  • the total amount of surfactant is from 25 to 65 wt.%, preferably from 25.5 to 50 wt.%.
  • surfactants such as amphoteric, zwitterionic and cationic surfactants may also be present in addition to the aforementioned nonionic and anionic surfactants.
  • cationic polysaccharide-based 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 branchpoints to ⁇ -1,6 linked galactose units.
  • An example of a 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.
  • preferred cationic cellulosic polymers include cocodimethylammonium hydroxypropyl oxyethyl cellulose, lauryldimethylammonium hydroxypropyl oxyethyl cellulose, stearyldimethylammonium hydroxypropyl oxyethyl cellulose, and stearyldimethylammonium hydroxyethyl cellulose; cellulose 2-hydroxyethyl 2-hydroxy 3-(trimethyl ammonio) propyl ether salt, polyquaternium-4, polyquaternium-10, polyquaternium-24 and polyquaternium-67 or mixtures thereof.
  • the cationic cellulosic polymer is polyquaternium-1 0.
  • Suitable commercial cationic cellulosic polymer products for use according to the present invention are marketed by the Amerchol Corporation, a subsidiary of The Dow Chemical Company, under the trade name UCARE Polymer LR-400.
  • cationic cellulosic polymer can include a single polymer or a mixture of different polymers.
  • 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 species responsible for providing a softening benefit in these formulations is a polymer/surfactant complex, especially a cationic polymer/soap complex.
  • the cationic polysaccharide-based polymer is present at a level of from 0.2 to 1.5 wt.%, preferably from 0.25 to 1 wt.%.
  • 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 polysaccharide-based polymer is from 10,000 to 850,000 Daltons, more preferably from 10,000 to 500,000 Daltons.
  • the liquid detergent composition may additionally comprise one or more of the following optional ingredients.
  • the composition optionally comprises from 1 to 50 wt.% of a builder.
  • the builder is present at a level of from 1 to 40 wt.%.
  • Builder materials may be selected from 1) calcium sequestrant materials, 2) precipitating materials, 3) calcium ion-exchange materials and 4) mixtures thereof.
  • the size is in the range 0.1 to 10 microns (as measured by The Mastersizer 2000 particle size analyzer using laser diffraction ex Malvern TM ).
  • calcium sequestrant builder materials examples include alkali metal polyphosphates, such as sodium tripolyphosphate and organic sequestrants, such as ethylene diamine tetra-acetic acid.
  • precipitating builder materials examples include sodium orthophosphate and sodium carbonate.
  • Examples of calcium ion-exchange builder materials include the various types of water-insoluble crystalline or amorphous aluminosilicates, of which zeolites are the best known representatives, e.g. zeolite A, zeolite B (also known as zeolite P), zeolite C, zeolite X, zeolite Y and also the zeolite P-type as described in EP-A-0,384,070 .
  • zeolites are the best known representatives, e.g. zeolite A, zeolite B (also known as zeolite P), zeolite C, zeolite X, zeolite Y and also the zeolite P-type as described in EP-A-0,384,070 .
  • the composition may also contain 0-50 wt.% of a builder or complexing agent such as ethylenediaminetetraacetic acid, diethylenetriamine-pentaacetic acid, alkyl- or alkenylsuccinic acid, nitrilotriacetic acid or the other builders mentioned below.
  • a builder or complexing agent such as ethylenediaminetetraacetic acid, diethylenetriamine-pentaacetic acid, alkyl- or alkenylsuccinic acid, nitrilotriacetic acid or the other builders mentioned below.
  • Many builders are also bleach-stabilising agents by virtue of their ability to complex metal ions.
  • Zeolite and carbonate are preferred builders.
  • the composition may contain as builder a crystalline aluminosilicate, preferably an alkali metal aluminosilicate, more preferably a sodium aluminosilicate. This is typically present at a level of less than 15 wt.%.
  • Aluminosilicates are materials having the general formula: 0.8-1.5 M 2 O. Al 2 O 3 . 0.8-6 SiO 2 where M is a monovalent cation, preferably sodium. These materials contain some bound water and are required to have a calcium ion exchange capacity of at least 50 mg CaO/g.
  • the preferred sodium aluminosilicates contain 1.5-3.5 SiO 2 units in the formula above. They can be prepared readily by reaction between sodium silicate and sodium aluminate, as amply described in the literature.
  • the ratio of surfactants to alumuminosilicate (where present) is preferably greater than 5:2, more preferably greater than 3:1.
  • phosphate builders may be used.
  • 'phosphate' embraces diphosphate, triphosphate, and phosphonate species.
  • Other forms of builder include silicates, such as soluble silicates, metasilicates, layered silicates (e.g. SKS-6 from Hoechst).
  • the laundry detergent formulation is a non-phosphate built laundry detergent formulation, i.e., contains less than 1 wt.% of phosphate.
  • the laundry treatment composition preferably comprises a blue or violet shading agent in the range from 0.0001 to 0.01 wt.%.
  • the shading agents reduce the perception of damage to many coloured garments and increase whiteness of white garments.
  • the shading agents are preferably selected from blue and violet dyes of the solvent disperse basic, direct and acid type listed in the colour index (Society of Dyers and Colourists and American Association of Textile Chemists and Colorists 2002).
  • a direct violet or direct blue dyes is present.
  • the dyes are bis-azo, tris-azo dyes or triphendioxazine dye.
  • the carcinogenic benzidene based dyes are not preferred.
  • 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 Fragrance Association
  • Many suitable examples of perfumes are provided in the CTFA (Cosmetic, Toiletry and Fragrance Association) 1992 International Buyers Guide, published by CFTA Publications and OPD 1993 Chemicals Buyers Directory 80th Annual Edition, published by Schnell Publishing Co .
  • 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.
  • Perfume and top note may be used to cue the fabric care benefit of the invention.
  • 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 are carboxymethylcellulose, poly(ethylene glycol), poly(vinyl alcohol), polycarboxylates such as polyacrylates, maleic/acrylic acid copolymers and lauryl methacrylate/acrylic acid copolymers.
  • 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, 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 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%.
  • Water, fluorescer and hydrotropes are mixed together at ambient temperature (approximately 22°C) for 2-3 minutes at a shear rate of 130 rpm using a Janke & Kunkel IKA RW20 overhead mixer. Salts and alkalis are added and mixed for 5 minutes prior to addition of surfactants and fatty acid. The temperature of the mix rises to around 50-60°C at this point. After allowing to cool to ⁇ 30C, the LR400 solution, PVP or PVP/PVI and remaining components such as perfume, preservatives, opacifier and dyes are added.
  • Formulations in table 2 were made according to the aforementioned method of production. The formulations were used to wash fabrics, which were then assessed for softness with a level of softness attributed to the washed fabrics. Softness testing took place in real washing machine tests conducted in typical European front-loading automatic machines. Washes were ⁇ 2 hours duration and included 2 rinses. Equal volumes of product (35ml) were tested.
  • the wash load consists of a 'ballast' portion made of cotton & poly-cotton sheets to achieve a 'standard' wash load weight of 2.5kg.
  • the cloths actually used to check for softness are pieces of terry-towelling, previously pre-harshened, which measure ⁇ 20 x 20cm. Cloths are line dried afterwards. 4 repeat washes are carried out to allow the softness effect to build up, after which the towelling monitors are assessed for softness.
  • the anionic surfactant used was LAS acid. This is neutralised in formulation to give sodium linear alkylbeneze sulphonate (NaLAS). The actual weight of anionic surfactant used is based on this neutralised form, and is therefore slightly higher than the formulation weight of LAS acid.
  • LAS acid has an average molecular weight of 326.5 based on a formula of (CH 3 (CH 2 ) 11 C 6 H 4 SO 3 H).
  • NaLAS has molecular weight of 348.5 based on a formula of (CH 3 (CH 2 ) 11 C 6 H 4 SO 3 Na).
  • An example value of 10g of LAS acid would have a total weight of anionic surfactant of 10.7g (based on the calculation (10g/326.5) x 348.5).
  • a comparative example was prepared according to WO 2008/022838 examples 1-3. According to the definitions herein, these example comprise nonionic surfactant at 12 wt.%, anonionic surfactant at 10.5 wt.% (made up from 7.5g NaLAS (rounded up from 10.47g) - i.e. the neutralised form of the acid + 3g of sodium xylenesulfonate, which is classed herein as both a surfactant and a hydrotrope), 10g of fatty acid and 0.45g of cationic polymer.
  • the total level of surfactant is 22.5g, the surfactant level as defined herein is not inclusive of the fatty acid or salt thereof.
  • Comparative B was similar to A, but with the nonionic and anionic surfactant scaled up to ⁇ 30% in total. Comparative examples C and D are further examples. The formulations were compared to a control formulation (Control) which did not contain any cationic polymer.
  • Table 2 Formula code Ratio of NI:An wt.% Non-Ionic wt.% Fatty Acid wt.% An wt.% Cationic Polymer Total Surfactant wt.% Ave.
  • formulations with a weight ratio of nonionic surfactant to anionic surfactant (NI:An ratio) within the range 1.25:1 to 2.25:1 are shown to have a superior effect on the softness of fabric when used in wash conditions.

Landscapes

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

Description

    FIELD OF THE INVENTION
  • This invention relates to a laundry composition. More particularly, the invention is directed to a softening in the wash laundry composition.
  • BACKGROUND OF THE INVENTION
  • Textile fabrics, including clothes, have traditionally been cleaned with laundry detergents. After cleaning, fabrics can often feel harsh and they will wear and lose colour over repeat wash cycles. To prevent the drawbacks of fabrics feeling harsh after cleaning and those experienced by multiple wash cycles, technologies have been developed to increase the softness of fabrics, including rinse-added conditioner compositions and softening systems added to the detergent composition.
  • One such softening system comprises a cationic polysaccharide and anionic surfactant. Such systems are known from WO 2004/069979 which discloses particular combinations of cationic polymers and anionic surfactants.
  • WO 2008/022838 discloses liquid laundry compositions comprising anionic surfactant, nonionic surfactant, fatty acid and cationic polymers. The compositions are stated to provide both effective softening and cleaning.
  • There still remains a need for softening laundry detergent compositions that provide improved softening.
  • WO2007/107215 A1 discloses a process for the preparation of a non-aqueous fabric treatment composition comprising a) provision of a pre-mix comprising cationic cellulose polymer, water and optional solvent; b) admixture of the pre-mix with anionic surfactant; and c) subsequent addition of non-ionic surfactant.
  • WO 2008/114171 A1 discloses a liquid laundry detergent comprising anionic surfactant, fabric core agent, cationic deposition aid and performance booster.
  • SUMMARY OF THE INVENTION
  • In a first aspect, this invention is directed to a liquid detergent composition comprising:-
    1. (a) from 6 to 40 wt.% nonionic surfactant;
    2. (b) from 6 to 20 wt.% anionic surfactant;
    3. (c) from 2 to 14 wt.% fatty acid or salt thereof;
    4. (d) from 0.2 to 1.5 wt.% cationic polysaccharide-based polymer; and,
      wherein,
    the weight ratio of (a) to (b) is from 1.25:1 to 2.25:1, and wherein the total level of surfactant present in the composition is at least 25 wt.%, and in accordance with claim 1.
  • In a second aspect, this invention is directed to a method for the provision of softness to a textile, comprising the steps:
    1. (a) provision of a liquid detergent composition as defined in the first aspect of the invention; and,
    2. (b) contacting one or more textile articles with the composition at one or more points during the main wash of a laundering process; and,
    3. (c) allowing the textile articles to dry or mechanically tumble-drying them.
    DETAILED DESCRIPTION OF THE INVENTION
  • As used herein, the term "comprising" means including, made up of, composed of, consisting and/or consisting essentially of.
  • All percentages quoted are wt.% unless otherwise stated.
  • Except in the operating and comparative examples, or where otherwise explicitly indicated, all numbers in this description indicating amounts or ratios of material or conditions of reaction, physical properties of materials and/or use are to be understood as modified by the word "about".
  • As used herein, a formula shall be considered physically "stable" when after 1 week at 21 degrees Celsius it exhibits no signs of phase separation.
  • The present invention is directed to laundry compositions containing fatty acid or salt thereof, a polysaccharide-based cationic polymer, a non-ionic surfactant and an anionic surfactant, wherein the ratio of nonionic to anionic surfactant is from 1.25:1 to 2.25:1, and wherein the total level of surfactant is at least 25 wt.% and in accordance with claim 1. The composition delivers a high level of softening to fabrics in comparison to the prior art. The composition also displays excellent stability.
  • Softening Benefits
  • The primary conditioning benefit afforded by these products is softening. Softening includes, but is not limited to, an improvement in the handling of a garment treated with the compositions of this invention relative to that of an article laundered under identical conditions but without the use of this invention. Consumers will often describe an article that is softened as "silky" or "fluffy", and generally prefer the feel of treated garments to those that are unsoftened.
  • The conditioning benefits of these compositions are not limited to just softening, however. They may, depending on the particular embodiment of the invention selected, also provide an antistatic benefit. In addition to softening, the cationic polymer/anionic surfactant compositions of this invention are further believed to lubricate the fibres of textile articles, which can reduce wear, pilling and colour fading, and provide a shape-retention benefit. This lubricating layer is also believed to provide a substrate on the fabric for retaining fragrances and other benefit agents.
  • Form of the Invention
  • The present invention can take any of a number of forms that are included as main wash products. It can take the form of a laundry treatment agent for the main wash, which may be dilutable or non-dilutable. The laundry treatment agent 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".
  • Softening in the Wash
  • By the term "softening in the wash" is meant a composition which provides a fabric softening benefit as well as providing cleaning to the laundered fabric. Such a composition can be added as part of a main wash product, or as a separate product for use in combination with another. However, for the purposes of this disclosure, the composition is intended for use in the main wash cycle. Preferably the softening in the wash composition of the invention is incorporated as part of a single product for use in the main wash.
  • The pH range of the composition is 7-12, preferably 8.5 to 9.5. It is desirable to buffer the formulation at whatever the target pH of the composition is.
  • Method of Use
  • The liquid detergent composition provides a softness benefit to the laundered fabrics by a method comprising the steps:
    1. (a) provision of a liquid detergent composition as defined in the first aspect of the invention; and,
    2. (b) contacting one or more textile articles with the composition at one or more points during the main wash of a laundering process; and,
    3. (c) allowing the textile articles to dry or mechanically tumble-drying them.
    Fatty Acid or Salt thereof
  • The liquid detergent compositions include fatty acid or salt thereof, a term used herein interchangeably with the term 'soap'. Both terms are herein defined as an alkali or alkaline earth metal salt of a natural or synthetic fatty acid containing between 6 and 30 carbon atoms. Preferably the soap contains between C8-C26, more preferably C8-C24, still more preferably C8-C18 carbon atoms. The incorporation level of the soap is from 2 to 14%, preferably from 2.5 to 10%, more preferably from 3 to 9% by weight of the total composition. Particularly preferred forms of soap are outlined below.
  • Carboxylic Acid Salts


  •         R1COOM

    where R 1 is a primary or secondary alkyl group of 5 to 29 carbon atoms and M is a solubilising cation. The alkyl group represented by R 1 may represent a mixture of chain lengths and may be saturated or unsaturated, although it is preferred that at least two thirds of the R 1 groups have a chain length of between 7 and 17 carbon atoms. Non-limiting examples of suitable alkyl group sources include the fatty acids derived from coconut oil, tallow, tall oil and palm kernel oil. For the purposes of minimising odour, however, it is often desirable to use primarily saturated carboxylic acids. Such materials are well known to those skilled in the art, and are available from many commercial sources, such as Uniqema (Wilmington, Del.) and Twin Rivers Technologies (Quincy, Mass.). The solubilising cation, M, is an alkali or alkaline earth metal cation. Preferred examples of cations include alkali metals such as sodium and potassium. Although, when used, the majority of the fatty acid should be incorporated into the formulation in neutralised salt form, it is often preferable to leave a small amount of free fatty acid in the formulation, as this can aid in the maintenance of product viscosity.
  • Surfactants
  • The liquid detergent composition comprises nonionic surfactant, and anionic surfactant other than soap. For the avoidance of doubt, the soap present in the composition is not included in the calculation of anionic surfactant for weight inclusion or weight ratios present in the composition. Thus the wt.% of soap present is not included the total amount of surfactant present.
  • They 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. Preferably 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 C6 to C22 alkyl phenolethylene oxide condensates, generally 5 to 25 EO, i.e. 5 to 25 units of ethylene oxide per molecule, and the condensation products of aliphatic C8 to C18 primary or secondary linear or branched alcohols with ethylene oxide, generally 5 to 40 EO.
  • Suitable anionic detergent compounds which may be used are usually watersoluble alkali metal salts of organic sulphates and sulphonates having alkyl radicals containing from about 8 to about 22 carbon atoms, the term alkyl being used to include the alkyl portion of higher acyl radicals. Examples of suitable synthetic anionic detergent compounds are sodium and potassium alkyl sulphates, especially those obtained by sulphating higher C8 to C18 alcohols, produced for example from tallow or coconut oil, sodium and potassium alkyl C9 to C20 benzene sulphonates, particularly sodium linear secondary alkyl C10 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 preferred anionic detergent compounds are sodium C11 to C15 alkyl benzene sulphonates and sodium C12 to C18 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 monoglycosides.
  • The nonionic detergent is present in amounts of from 6 to 40 wt.%, preferably from 7.5 to 35 wt.%, more preferably from 10 to 25 wt.%.
  • The anionic surfactant is present in amounts of from 6 to 20 wt.%, preferably from 6.5 to 17.5 wt.%, more preferably from 7.5 to 15 wt.%.
  • The ratio of nonionic surfactant to anionic surfactant present in the liquid composition is from 1.25:1 to 2.25:1, based on weight.
  • The total amount of surfactant present in the liquid composition is at least 25 wt.%. Preferably the total amount of surfactant is from 25 to 65 wt.%, preferably from 25.5 to 50 wt.%.
  • Other surfactants such as amphoteric, zwitterionic and cationic surfactants may also be present in addition to the aforementioned nonionic and anionic surfactants.
  • Cationic Polysaccharide-based Polymer
  • The term "cationic polysaccharide-based 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. Preferably the quaternary ammonium salt is linked to the polysaccharide backbone by a hydroxyethyl or hydroxypropyl group. Preferably 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 β-1,4 linked mannose backbone with branchpoints to α-1,6 linked galactose units. An example of a 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 β-1,4 glycosidic bonds and is a linear, non-branched polymer. Typical examples of preferred cationic cellulosic polymers include cocodimethylammonium hydroxypropyl oxyethyl cellulose, lauryldimethylammonium hydroxypropyl oxyethyl cellulose, stearyldimethylammonium hydroxypropyl oxyethyl cellulose, and stearyldimethylammonium hydroxyethyl cellulose; cellulose 2-hydroxyethyl 2-hydroxy 3-(trimethyl ammonio) propyl ether salt, polyquaternium-4, polyquaternium-10, polyquaternium-24 and polyquaternium-67 or mixtures thereof.
  • More preferably the cationic cellulosic polymer is polyquaternium-1 0. Suitable commercial cationic cellulosic polymer products for use according to the present invention are marketed by the Amerchol Corporation, a subsidiary of The Dow Chemical Company, under the trade name UCARE Polymer LR-400.
  • The term cationic cellulosic polymer can include a single polymer or a mixture of different polymers.
  • 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.
  • Without wishing to be bound by theory, it is believed that the species responsible for providing a softening benefit in these formulations is a polymer/surfactant complex, especially a cationic polymer/soap complex.
  • The cationic polysaccharide-based polymer is present at a level of from 0.2 to 1.5 wt.%, preferably from 0.25 to 1 wt.%.
  • Many of the aforementioned cationic polymers can be synthesised in, and are commercially available in, a number of different molecular weights. Preferably the molecular weight of the cationic polysaccharide-based polymer is from 10,000 to 850,000 Daltons, more preferably from 10,000 to 500,000 Daltons.
  • Optional Ingredients
  • The liquid detergent composition may additionally comprise one or more of the following optional ingredients.
  • Builders or Complexing Agents
  • The composition optionally comprises from 1 to 50 wt.% of a builder. Preferably the builder is present at a level of from 1 to 40 wt.%.
  • Builder materials may be selected from 1) calcium sequestrant materials, 2) precipitating materials, 3) calcium ion-exchange materials and 4) mixtures thereof.
  • It is preferred that when an insoluble inorganic builder, e.g., zeolite is used, the size is in the range 0.1 to 10 microns (as measured by The Mastersizer 2000 particle size analyzer using laser diffraction ex Malvern).
  • Examples of calcium sequestrant builder materials include alkali metal polyphosphates, such as sodium tripolyphosphate and organic sequestrants, such as ethylene diamine tetra-acetic acid.
  • Examples of precipitating builder materials include sodium orthophosphate and sodium carbonate.
  • Examples of calcium ion-exchange builder materials include the various types of water-insoluble crystalline or amorphous aluminosilicates, of which zeolites are the best known representatives, e.g. zeolite A, zeolite B (also known as zeolite P), zeolite C, zeolite X, zeolite Y and also the zeolite P-type as described in EP-A-0,384,070 .
  • The composition may also contain 0-50 wt.% of a builder or complexing agent such as ethylenediaminetetraacetic acid, diethylenetriamine-pentaacetic acid, alkyl- or alkenylsuccinic acid, nitrilotriacetic acid or the other builders mentioned below. Many builders are also bleach-stabilising agents by virtue of their ability to complex metal ions.
  • Zeolite and carbonate (carbonate (including bicarbonate and sesquicarbonate) are preferred builders.
  • The composition may contain as builder a crystalline aluminosilicate, preferably an alkali metal aluminosilicate, more preferably a sodium aluminosilicate. This is typically present at a level of less than 15 wt.%. Aluminosilicates are materials having the general formula:

            0.8-1.5 M2O. Al2O3. 0.8-6 SiO2

    where M is a monovalent cation, preferably sodium. These materials contain some bound water and are required to have a calcium ion exchange capacity of at least 50 mg CaO/g. The preferred sodium aluminosilicates contain 1.5-3.5 SiO2 units in the formula above. They can be prepared readily by reaction between sodium silicate and sodium aluminate, as amply described in the literature. The ratio of surfactants to alumuminosilicate (where present) is preferably greater than 5:2, more preferably greater than 3:1.
  • Alternatively, or additionally to the aluminosilicate builders, phosphate builders may be used. In this art the term 'phosphate' embraces diphosphate, triphosphate, and phosphonate species. Other forms of builder include silicates, such as soluble silicates, metasilicates, layered silicates (e.g. SKS-6 from Hoechst).
  • Preferably the laundry detergent formulation is a non-phosphate built laundry detergent formulation, i.e., contains less than 1 wt.% of phosphate.
  • Shading Agent
  • The laundry treatment composition preferably comprises a blue or violet shading agent in the range from 0.0001 to 0.01 wt.%. The shading agents reduce the perception of damage to many coloured garments and increase whiteness of white garments.
  • The shading agents are preferably selected from blue and violet dyes of the solvent disperse basic, direct and acid type listed in the colour index (Society of Dyers and Colourists and American Association of Textile Chemists and Colorists 2002).
  • Preferably a direct violet or direct blue dyes is present. Preferably the dyes are bis-azo, tris-azo dyes or triphendioxazine dye. The carcinogenic benzidene based dyes are not preferred.
  • Fluorescent Agent
  • 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. Tinopal DMS pure Xtra and Blankophor (Trade Mark) HRH, and Pyrazoline compounds, e.g. Blankophor SN. 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.
  • Perfume
  • Preferably 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.%. Many suitable examples of perfumes are provided in the CTFA (Cosmetic, Toiletry and Fragrance Association) 1992 International Buyers Guide, published by CFTA Publications and OPD 1993 Chemicals Buyers Directory 80th Annual Edition, published by Schnell Publishing Co.
  • It is commonplace for a plurality of perfume components to be present in a formulation. In the 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.
  • In perfume mixtures preferably 15 to 25 wt.% are top notes. 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.
  • Perfume and top note may be used to cue the fabric care benefit of the invention.
  • It is preferred that the laundry treatment composition does not contain a peroxygen bleach, e.g., sodium percarbonate, sodium perborate, and peracid.
  • Polymers
  • The composition may comprise one or more polymers. Examples are carboxymethylcellulose, poly(ethylene glycol), poly(vinyl alcohol), polycarboxylates such as polyacrylates, maleic/acrylic acid copolymers and lauryl methacrylate/acrylic acid copolymers.
  • Hydrotrope
  • The liquid detergent composition may optionally include 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, 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. Preferably, the 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%.
  • Examples Method of Production
  • Water, fluorescer and hydrotropes are mixed together at ambient temperature (approximately 22°C) for 2-3 minutes at a shear rate of 130 rpm using a Janke & Kunkel IKA RW20 overhead mixer. Salts and alkalis are added and mixed for 5 minutes prior to addition of surfactants and fatty acid. The temperature of the mix rises to around 50-60°C at this point. After allowing to cool to <30C, the LR400 solution, PVP or PVP/PVI and remaining components such as perfume, preservatives, opacifier and dyes are added.
  • Example Formulations
  • Table 1
    Ingredient 1 %.wt 2 %.wt 3 %.wt 4 %.wt
    LAS ACID (Surfactant) 10 10 10 10
    NEODOL 25-7E (Surfactant) 20 20 20 20
    PRIFAC 5908 (Fatty Acid) 6 10 6 6
    PROPYLENE GLYCOL (Hydrotrobe) 9 9 9 9
    GLYCEROL (Hydrotrope) 5 5 5 5
    SODIUM HYDROXIDE (Alkali) 2.2 2.5 2.2 2.2
    TRIETHANOLAMINE (Alkali) 6 6 6 6
    TINOPAL CBS-X (Fluorescer) 0.1 0.1 - -
    Polyvinylpyrrolidone (PVP K15) 0.35 0.35 0.35 -
    PVP/PVI (Poly Vinyl Pyrrolidone-co-Poly Vinyl Imidazole) - - - 0.65
    LR400 (Cationic polymer) 0.45 0.43 0.43 0.43
    PROXEL GXL (Preservative) 0.04 0.04 0.01 0.01
    SODIUM CHLORIDE (Salt) 0.5 0.5 0.5 0.5
    ACUSOL OP31 (Opacifier) 0.05 0.05 0.05 0.05
    PATENT BLUE V85 (Dye) 0.00068 0.00068 0.00068 0.00068
    ACID YELLOW 23 (Dye) 0.0001 0.0001 0.0001 0.0001
    PERFUME 1-1.3 1.1 1.39 1.39
    WATER TO 100 TO 100 TO 100 TO 100
  • Softening Data
  • Formulations in table 2 were made according to the aforementioned method of production. The formulations were used to wash fabrics, which were then assessed for softness with a level of softness attributed to the washed fabrics. Softness testing took place in real washing machine tests conducted in typical European front-loading automatic machines. Washes were ∼2 hours duration and included 2 rinses. Equal volumes of product (35ml) were tested.
  • The wash load consists of a 'ballast' portion made of cotton & poly-cotton sheets to achieve a 'standard' wash load weight of 2.5kg. The cloths actually used to check for softness are pieces of terry-towelling, previously pre-harshened, which measure ∼20 x 20cm. Cloths are line dried afterwards. 4 repeat washes are carried out to allow the softness effect to build up, after which the towelling monitors are assessed for softness. Softness assessment was carried out by a panel of volunteers. They were asked to rank the towels in order of softest to harshest, using a 7-point scale (1 =softest, 7=harshest). The scores for a given product were added up and the average value calculated.
  • The anionic surfactant used was LAS acid. This is neutralised in formulation to give sodium linear alkylbeneze sulphonate (NaLAS). The actual weight of anionic surfactant used is based on this neutralised form, and is therefore slightly higher than the formulation weight of LAS acid. LAS acid has an average molecular weight of 326.5 based on a formula of (CH3(CH2)11C6H4SO3H). NaLAS has molecular weight of 348.5 based on a formula of (CH3(CH2)11C6H4SO3Na). An example value of 10g of LAS acid would have a total weight of anionic surfactant of 10.7g (based on the calculation (10g/326.5) x 348.5).
  • A comparative example (comparative A) was prepared according to WO 2008/022838 examples 1-3. According to the definitions herein, these example comprise nonionic surfactant at 12 wt.%, anonionic surfactant at 10.5 wt.% (made up from 7.5g NaLAS (rounded up from 10.47g) - i.e. the neutralised form of the acid + 3g of sodium xylenesulfonate, which is classed herein as both a surfactant and a hydrotrope), 10g of fatty acid and 0.45g of cationic polymer. The total level of surfactant is 22.5g, the surfactant level as defined herein is not inclusive of the fatty acid or salt thereof. Comparative B was similar to A, but with the nonionic and anionic surfactant scaled up to ∼30% in total. Comparative examples C and D are further examples. The formulations were compared to a control formulation (Control) which did not contain any cationic polymer. Table 2
    Formula code Ratio of NI:An wt.% Non-Ionic wt.% Fatty Acid wt.% An wt.% Cationic Polymer Total Surfactant wt.% Ave. Soft Score
    Control 0.96:1 20.1 4.8 21 0 41.1 6.7
    Comparative A 1.15 : 1 12 10 10.5 0.45 22.5 5.1
    Comparative B 1.2 : 1 16 10 13.4 0.45 29.4 6.2
    Comparative C 0.94 : 1 15 10 16 0.45 31 3.7
    Comparative D 0.47 : 1 10 10 21.3 0.45 31.3 3.3
    Invention 1 1.41 : 1 18 10 12.8 0.45 30.8 1.7
    Invention 2 1.87 : 1 20 10 10.7 0.45 30.7 1.3
  • The softening scores are presented as a lower score = a better softness level. As is clear from the table, formulations with a weight ratio of nonionic surfactant to anionic surfactant (NI:An ratio) within the range 1.25:1 to 2.25:1 are shown to have a superior effect on the softness of fabric when used in wash conditions.

Claims (7)

  1. A liquid detergent composition comprising:-
    (a) from 6 to 40 wt.% nonionic surfactant;
    (b) from 6 to 20 wt.% anionic surfactant;
    (c) from 2 to 14 wt.% fatty acid or salt thereof;
    (d) from 0.2 to 1.5 wt.% cationic polysaccharide-based polymer;
    wherein the weight ratio of (a) to (b) is from 1.25:1 to 2.25:1;
    the total level of surfactant present in the composition is at least 25 wt.%; and wherein the total level of surfactant is calculated by the total of nonionic surfactant; anionic surfactant which includes all salts of sulphonates, but not soap; amphoteric; zwitterionic; and cationic surfactants.
  2. A composition according to claim 1 wherein the nonionic surfactant is present at a level of from 7.5 to 35 wt.%, preferably from 10 to 25 wt.%.
  3. A composition according to claim 1 or claim 2 wherein the anionic surfactant is present at a level of from 6.5 to 17.5 wt.%, preferably from 7.5 to 15 wt.%.
  4. A composition according to any preceding claim, wherein the cationic polysaccharide-based polymer is present at a level of from 0.25 to 1 wt.%.
  5. A composition according to any preceding claim, wherein the fatty acid or salt thereof is present at a level of from 2.5 to 10 wt.%, preferably from 3 to 9% wt.%.
  6. A composition according to any preceding claim, wherein the cationic polysaccharide-based polymer is a cationic cellulose based polymer.
  7. A method for the provision of softness to a textile, comprising the steps:
    (a) provision of a liquid detergent composition according to any one of claims 1 to 6; and,
    (b) contacting one or more textile articles with the composition at one or more points during the main wash of a laundering process; and,
    (c) allowing the textile articles to dry or mechanically tumble-drying them.
EP09771385A 2008-12-22 2009-12-16 Laundry compositions Active EP2366008B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP09771385A EP2366008B1 (en) 2008-12-22 2009-12-16 Laundry compositions

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP08172508 2008-12-22
PCT/EP2009/067256 WO2010072627A1 (en) 2008-12-22 2009-12-16 Laundry compositions
EP09771385A EP2366008B1 (en) 2008-12-22 2009-12-16 Laundry compositions

Publications (2)

Publication Number Publication Date
EP2366008A1 EP2366008A1 (en) 2011-09-21
EP2366008B1 true EP2366008B1 (en) 2012-09-05

Family

ID=40652741

Family Applications (1)

Application Number Title Priority Date Filing Date
EP09771385A Active EP2366008B1 (en) 2008-12-22 2009-12-16 Laundry compositions

Country Status (7)

Country Link
EP (1) EP2366008B1 (en)
CN (1) CN102257116B (en)
AR (1) AR074849A1 (en)
BR (1) BRPI0923571A2 (en)
ES (1) ES2393529T3 (en)
WO (1) WO2010072627A1 (en)
ZA (1) ZA201104027B (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6247234B2 (en) * 2012-03-15 2017-12-13 アジェンデ・キミケ・リウニテ・アンジェリニ・フランチェスコ・ア・チ・エレ・ア・エフェ・ソシエタ・ペル・アチオニAziende Chimiche Riunite Angelini Francesco A.C.R.A.F.Societa Per Azioni Glycogen-based cationic polymer
EP2909295B1 (en) * 2012-10-17 2016-08-03 Unilever PLC Laundry compositions
CN105838514A (en) * 2016-03-29 2016-08-10 江南大学 Liquid detergent containing gemini surfactant
EP3293251A1 (en) * 2016-09-07 2018-03-14 The Procter & Gamble Company Use of cationically modified polysaccharide polymer for improved brightener deposition
EP3293250A1 (en) 2016-09-07 2018-03-14 The Procter & Gamble Company A liquid detergent composition comprising cellulosic polymers and cellulase
ES2809719T3 (en) 2016-09-07 2021-03-05 Procter & Gamble A liquid laundry detergent composition comprising a first polymer and a second polymer
US20220220420A1 (en) * 2019-05-16 2022-07-14 Conopco, lnc., d/b/a UNILEVER Laundry composition

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BRPI0407114B1 (en) * 2003-02-03 2018-09-11 Unilever Nv laundry composition
GB0605512D0 (en) 2006-03-18 2006-04-26 Unilever Plc Fabric treatment composition and process for preparation thereof
US20080045438A1 (en) * 2006-08-21 2008-02-21 D/B/A Unilever, A Corporation Of New York Softening laundry detergent
US20080234165A1 (en) 2007-03-20 2008-09-25 Rajan Keshav Panandiker Liquid laundry detergent compositions comprising performance boosters

Also Published As

Publication number Publication date
BRPI0923571A2 (en) 2016-08-23
ES2393529T3 (en) 2012-12-26
ZA201104027B (en) 2012-08-29
CN102257116B (en) 2013-02-06
CN102257116A (en) 2011-11-23
WO2010072627A1 (en) 2010-07-01
EP2366008A1 (en) 2011-09-21
AR074849A1 (en) 2011-02-16

Similar Documents

Publication Publication Date Title
EP2791308B1 (en) Laundry compositions
EP2791310B1 (en) Laundry compositions
EP2922936B1 (en) Laundry compositions
EP3074495B1 (en) Laundry compositions
EP2909295B1 (en) Laundry compositions
EP2366008B1 (en) Laundry compositions
EP1735418B1 (en) Softening laundry detergent
EP3074497B1 (en) Laundry compositions
CA2575015A1 (en) Softening laundry detergent
AU2006232785B2 (en) Fabric softening composition with cationic polymer, soap, and amphoteric surfactant
EP1866400A1 (en) Fabric softening composition
EP2366009B1 (en) Laundry compositions
WO2013087285A1 (en) Laundry compositions and uses
EP2922938B1 (en) Laundry compositions
EP2922937B1 (en) Ingredient for use in a laundry composition
EP3327106A1 (en) Easy ironing/anti-wrinkle/less crease benefit by use of cationic polymers and its derivatives
EP2491103B1 (en) Laundry compositions

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20110616

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO SE SI SK SM TR

DAX Request for extension of the european patent (deleted)
GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO SE SI SK SM TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: AT

Ref legal event code: REF

Ref document number: 574161

Country of ref document: AT

Kind code of ref document: T

Effective date: 20120915

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602009009546

Country of ref document: DE

Effective date: 20121031

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2393529

Country of ref document: ES

Kind code of ref document: T3

Effective date: 20121226

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 574161

Country of ref document: AT

Kind code of ref document: T

Effective date: 20120905

REG Reference to a national code

Ref country code: NL

Ref legal event code: VDEP

Effective date: 20120905

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

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20120905

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20120905

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20120905

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20120905

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20121205

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG4D

Effective date: 20120905

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

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20120905

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20120905

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20121206

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20120905

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

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20120905

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20120905

Ref country code: BE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20120905

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130105

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20120905

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20120905

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

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130107

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20120905

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20120905

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

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

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

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

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20120905

Ref country code: MC

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

Effective date: 20121231

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20121205

26N No opposition filed

Effective date: 20130606

REG Reference to a national code

Ref country code: IE

Ref legal event code: MM4A

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602009009546

Country of ref document: DE

Effective date: 20130606

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

Ref country code: IE

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

Effective date: 20121216

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

Ref country code: MT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20120905

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20120905

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

Ref country code: LU

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

Effective date: 20121216

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20120905

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

Ref country code: HU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20091216

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

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

Ref country code: LI

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

Effective date: 20131231

Ref country code: CH

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

Effective date: 20131231

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

Ref country code: MK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20120905

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 7

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 8

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

Ref country code: ES

Payment date: 20161213

Year of fee payment: 8

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

Ref country code: IT

Payment date: 20161227

Year of fee payment: 8

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 9

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

Ref country code: IT

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

Effective date: 20171216

REG Reference to a national code

Ref country code: ES

Ref legal event code: FD2A

Effective date: 20190703

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

Ref country code: ES

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

Effective date: 20171217

REG Reference to a national code

Ref country code: DE

Ref legal event code: R081

Ref document number: 602009009546

Country of ref document: DE

Owner name: UNILEVER GLOBAL IP LIMITED, WIRRAL, GB

Free format text: FORMER OWNER: UNILEVER N.V., ROTTERDAM, NL

REG Reference to a national code

Ref country code: GB

Ref legal event code: 732E

Free format text: REGISTERED BETWEEN 20220203 AND 20220209

P01 Opt-out of the competence of the unified patent court (upc) registered

Effective date: 20230428

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

Ref country code: GB

Payment date: 20231220

Year of fee payment: 15

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

Ref country code: FR

Payment date: 20231221

Year of fee payment: 15

Ref country code: DE

Payment date: 20231214

Year of fee payment: 15

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

Ref country code: TR

Payment date: 20231215

Year of fee payment: 15