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Laundry Compositions

Abstract: The present invention relates to a liquid detergent composition comprising at least 25 wt.% surfactant, comprising (a) nonionic surfactant, (b) anionic surfactant, (c) fatty acid or salt thereof and (d) a cationic polysaccharide-based polymer, wherein weight ratio of (a) to (c) is from 2.5:1 to 6:1; the composition being useful in providing fabric softness during laundering.

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Patent Information

Application #
Filing Date
17 June 2011
Publication Number
01/2012
Publication Type
INA
Invention Field
CHEMICAL
Status
Email
Parent Application

Applicants

HINDUSTAN UNILEVER LIMITED
HINDUSTAN UNILEVER HOUSE, 165-166 BACKBAY RECLAMATION, MUMBAI, 400 020, INDIA

Inventors

1. BULLEN GILLIAN ELAINE
UNILEVER R&D PORT SUNLIGHT, QUARRY ROAD EAST, BEBINGTON, WIRRAL, MERSEYSIDE CH63 3JW, UNITED KINGDOM
2. JEAN-DENIS BERNARD
182 MILL LANE, WAVERTREE, LIVERPOOL, L15 8LJ, UNITED KINGDOM
3. RIGBY DAWN
UNILEVER R&D PORT SUNLIGHT, QUARRY ROAD EAST, BEBINGTON, WIRRAL, MERSEYSIDE CH63 3JW, UNITED KINGDOM
4. SALE GRAHAM PHILIP
UNILEVER R&D PORT SUNLIGHT, QUARRY ROAD EAST, BEBINGTON, WIRRAL, MERSEYSIDE, CH63 3JW, UNITED KINGDOM

Specification

FORM - 2
THE PATENTS ACT, 1970
(39 of 1970)
&
The Patents Rules, 2003
COMPLETE SPECIFICATION
(See Section 10 and Rule 13)
LAUNDRY COMPOSITIONS
HINDUSTAN UNILEVER LIMITED, a company incorporated under
the Indian Companies Act, 1913 and having its registered office
at 165/166, Backbay Reclamation, Mumbai -400 020, Maharashtra, India
The following specification particularly describes the invention and the manner in which it is to be performed

LAUNDRY COMPOSITIONS
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 fee! 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. The exemplified surfactant levels are generally low. For cleaning purposes, it is preferred to provide detergent compositions with higher surfactant concentrations. However, a problem with the prior art formulations at higher surfactant levels is that they can be unstable formulations.
WO 2008/022838 discloses liquid laundry compositions comprising anionic surfactant, nonionic surfactant, fatty acid and a cationic polymer. The compositions are stated to provide both effective softening and cleaning.

WO 2007/107215 discloses a process for the preparation of a non-aqueous liquid composition. The composition comprises anionic surfactant, nonionic surfactant, fatty acid and a cationic polymer.
There is thus a need for softening laundry detergent compositions with higher surfactant levels that have improved stability.
SUMMARY OF THE INVENTION
\n a first aspect, this invention is directed to 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 saft thereof;
(d) from 0.2 to 1.5 wt.% cationic polysaccharide-based polymer; and, wherein,
the weight ratio of (a) to (c) is from 2.5:1 to 6:1, and wherein the total level of surfactant present in the composition is at least 25 vvt.%-
Preferably the weight ratio of (a) to (c) is from 2.5:1 to 5:1, more preferably from 3:1 to 4.5:1.
In a second aspect, this invention is directed to a method for the provision of softness to a textile, comprising the steps:
(a) provision of a liquid detergent composition as defined in the first aspect of the invention; 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.
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 nonionic surfactant and an anionic surfactant, wherein the ratio of nonionic surfactant to fatty acid or salt thereof is from 2.5:1 to 6:1, and wherein the total level of surfactant is at least 25 wt.%. The composition displays improved stability over the prior art, and further delivers excellent softening.
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/an ionic surfactant compositions of this invention are further believed to lubricate the fibres of textile articles, which can reduce wear, pilling and colour lading, 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:
(a) provision of a liquid detergent composition as defined in the first aspect of the invention; 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.
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 R1 is a primary or secondary alkyl group of 5 to 29 carbon atoms and M is a soiubiiising cation. The alkyl group represented by R1 may represent a mixture of chain lengths and may be saturated or unsaturated, although it is preferred that at least two thirds of the R1 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 soiubiiising 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 fiquid detergent composition comprises nonfonic 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.
The liquid detergent compositions have a high level of surfactant present defined as a surfactant level of at least 25 wt.% of the composition.
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 HauserVerlag, 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 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 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 water-soluble 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 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 Polvsaccharide-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 hydroxy! groups of the polysaccharide backbone to give an overall positive charge to the modified celiulosic 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 (3-1,4 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 oxyethyi cellulose, lauryldimethylammonium hydroxypropyl oxyethyi cellulose, stearyldimethylammonium hydroxypropyl oxyethyi 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-10. 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 Complexinq 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. Al203. 0.8-6 Si02
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-sulfopheny!)-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 carboxymethylceflulose, poly(ethylene glycol), pofy(vinyl alcohol), polycarboxylates such as polyacrylates, maleic/acrylic acid copolymers and lauryl methacrylate/acrylic acid copolymers.
Hydrotrobe
The liquid detergent composition may optionally incfude 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 5 %.wt
LAS ACID (Surfactant) 10 10 10 10 10
NEODOL 25-7E (Surfactant) 20 20 27 20 20
PRIFAC 5908 (Fatty Acid) 6 10 6 6 6
PROPYLENE-GLYCOL (Hydrotrobe) 9 9 9 9 9
GLYCEROL (Hydrotrobe) 5 5 5 5 5
SODIUM HYDROXIDE (Alkali) 2.2 2.5 2.2 2.2 2.2
TRIETHANOLAMINE (Alkali) 6 6 6 6 6
TINOPAL CBS-X (Fluorescer) 0.1 0.1 0.1
Polyvinylpyrrolidone (PVP K15) 0.35 0.35 0.35 0.35
PVP/PVI
(Poly Vinyl Pyrrolidone-co-
Poly Vinyl Imidazole) 0.65
LR400 (Cationic polymer) 0.45 0.43 0.45 0.43 0.43
PROXEL GXL (Preservative) 0.04 0.04 0.04 0.01 0.01
SODIUM CHLORIDE (Salt) 0.5 0.5 0.5 0.5 0.5
ACUSOL OP31 (Opacifier) 0.05 0.05 0.05 0.05 0.05
PATENT BLUE V85 (Dye) 0.00068 0.00068 0.00068 0.00068 0.00068
ACID YELLOW 23 (Dye) 0.0001 0.0001 0.0001 0.0001 0.0001
PERFUME 1-1.3 1.1 1.1 1.39 1.39
WATER TO 100 TO 100 TO 100 TO 100 TO 100

Stability Experiment Formulations
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 10.67g (based on the calculation (10g/326.5) x 348.5).
Comparative examples A and B were prepared as described earlier. Example A has a nonionic surfactant to soap weight ratio (NI:Soap) of 0.5:1, while example B has a Nl:Soap ratio of 10:1, i.e. outside the lower and upper range present in claim 1. Example A proved to be unstable during processing.
A comparative example (Comparative C) 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 hydrotrobe), 10g of fatty acid and 0.5g 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. This example thus has a nonionic surfactant to soap weight ratio of 1.2:1. Comparative example D was similar to C, but with the nonionic and anionic surfactant scaled up to -30% in total. All examples 1-4 and comparative examples A-D in table 2 comprised 0.45 wt.% of cationic polymer (LR400).

Stability Experiment
Samples of 100ml are stored in clear, plastic jars for a period of up to 12 weeks. Storage took place at room temperature (22°C) and the samples were assessed for physical instability in terms of phase separation, defined as being the development of two, or more layers present in the sample. It is thus possible to assess the products in terms of whether they display instability, or indeed if they can be processed to a completed product at all. The following table shows the physical stability characteristics of a series of formulations made according to the aforementioned method of production.
Table 2

Formula code Ratio of wt.% wt.% wt.% Total Sur- Stability
NI:An Nl FA An factant wt.%
Comparative 1 :2 10 20 10.7 20.7 Unstable
A (couldn't be made)
Comparative 10: 1 40 4 10.7 50.7 Unstable
B (Phase separation)
Comparative 1.2:1 12 10 10.5 22.5 Unstable
C (Phase separation)
Comparative 1.2:1 16 10 13.4 29.4 Unstable
D (Phase separation)
Invention 2.5:1 15 6 10.7 25.7 Stable
1 (after 12 weeks)
Invention 3:1 18 6 10.7 28.8 Stable
2 (after 12 weeks)
Invention 3.3:1 20 6 10.7 30.7 Stable
3 (after 12 weeks)
Invention 4.5:1 27 6 10.7 37.7 Stable
4 (after 12 weeks)
As is clear from the table, formulations with a weight ratio of nonionic surfactant to fatty acid within the range 2.5:1 to 6:1 are shown to have more stable.

CLAIMS
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 poiysaccharide-based polymer; and, wherein,
the weight ratio of (a) to (c) is from 2.5:1 to 6:1, and wherein the total level of surfactant present in the composition is at least 25 wt.%.
2. The 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. The 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. The 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. The 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 weight ratio of nonionic to fatty acid or salt thereof is from 2.5:1 to 5:1, preferably from 3:1 to 4.5:1.

7. A composition according to any preceding claim, wherein the cationic polysaccharide-based polymer is a cationic cellulose based polymer.
8. 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 7; 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.

Documents

Application Documents

# Name Date
1 1250-mumnp-2011-claims.doc 2018-08-10
1 1250-MUMNP-2011-FORM 3(10-12-2013).pdf 2013-12-10
2 1250-mumnp-2011-claims.pdf 2018-08-10
2 1250-MUMNP-2011-FORM 3(10-11-2014).pdf 2014-11-10
3 1250-MUMNP-2011-FORM 3-(25-04-2015).pdf 2015-04-25
3 1250-MUMNP-2011-CORRESPONDENCE(10-9-2012).pdf 2018-08-10
4 1250-MUMNP-2011-CORRESPONDENCE-(16-03-2016).pdf 2016-03-16
4 1250-MUMNP-2011-CORRESPONDENCE(8-8-2011).pdf 2018-08-10
5 1250-mumnp-2011-correspondence.pdf 2018-08-10
5 1250-MUMNP-2011-ASSIGNMENT-(16-03-2016).pdf 2016-03-16
6 OTHERS [03-06-2016(online)].pdf 2016-06-03
6 1250-mumnp-2011-description(complete).pdf 2018-08-10
7 Examination Report Reply Recieved [03-06-2016(online)].pdf 2016-06-03
7 1250-mumnp-2011-form 1.pdf 2018-08-10
8 Description(Complete) [03-06-2016(online)].pdf 2016-06-03
8 1250-MUMNP-2011-FORM 13(14-2-2012).pdf 2018-08-10
9 1250-MUMNP-2011-FORM 18(10-9-2012).pdf 2018-08-10
9 Correspondence [03-06-2016(online)].pdf 2016-06-03
10 1250-mumnp-2011-form 2(title page).pdf 2018-08-10
10 Abstract [03-06-2016(online)].pdf 2016-06-03
11 Other Document [15-05-2017(online)].pdf 2017-05-15
12 1250-mumnp-2011-form 2.pdf 2018-08-10
12 Form 26 [15-05-2017(online)].pdf 2017-05-15
13 1250-MUMNP-2011-FORM 3(12-8-2011).pdf 2018-08-10
13 Form 13 [15-05-2017(online)].pdf 2017-05-15
14 1250-MUMNP-2011-FORM 3(15-2-2012).pdf 2018-08-10
14 1250-MUMNP-2011-ORIGINAL UNDER RULE 6 (1A)-22-05-2017.pdf 2017-05-22
15 1250-MUMNP-2011-FORM 3(21-5-2014).pdf 2018-08-10
15 1250-MUMNP-2011_EXAMREPORT.pdf 2018-08-10
16 1250-MUMNP-2011-FORM 3(22-6-2013).pdf 2018-08-10
16 1250-mumnp-2011-wo international publication report a1.pdf 2018-08-10
17 1250-mumnp-2011-other document.pdf 2018-08-10
17 1250-MUMNP-2011-FORM 3(23-1-2013).pdf 2018-08-10
18 1250-MUMNP-2011-Original Under Rule 6(1 A)Form 3-250117.pdf 2018-08-10
18 1250-MUMNP-2011-FORM 3(8-8-2012).pdf 2018-08-10
19 1250-MUMNP-2011-Form 3-081015.pdf 2018-08-10
19 1250-MUMNP-2011-HearingNoticeLetter.pdf 2018-08-10
20 1250-MUMNP-2011-Form 3-120816.pdf 2018-08-10
20 1250-MUMNP-2011-GENERAL POWER OF ATTORNEY(8-8-2011).pdf 2018-08-10
21 1250-MUMNP-2011-Form 3-190316.pdf 2018-08-10
21 1250-mumnp-2011-form pct-isa-210.pdf 2018-08-10
22 1250-mumnp-2011-form 3.pdf 2018-08-10
22 1250-mumnp-2011-form 5.pdf 2018-08-10
23 1250-mumnp-2011-form 3.pdf 2018-08-10
23 1250-mumnp-2011-form 5.pdf 2018-08-10
24 1250-mumnp-2011-form pct-isa-210.pdf 2018-08-10
24 1250-MUMNP-2011-Form 3-190316.pdf 2018-08-10
25 1250-MUMNP-2011-Form 3-120816.pdf 2018-08-10
25 1250-MUMNP-2011-GENERAL POWER OF ATTORNEY(8-8-2011).pdf 2018-08-10
26 1250-MUMNP-2011-Form 3-081015.pdf 2018-08-10
26 1250-MUMNP-2011-HearingNoticeLetter.pdf 2018-08-10
27 1250-MUMNP-2011-FORM 3(8-8-2012).pdf 2018-08-10
27 1250-MUMNP-2011-Original Under Rule 6(1 A)Form 3-250117.pdf 2018-08-10
28 1250-MUMNP-2011-FORM 3(23-1-2013).pdf 2018-08-10
28 1250-mumnp-2011-other document.pdf 2018-08-10
29 1250-MUMNP-2011-FORM 3(22-6-2013).pdf 2018-08-10
29 1250-mumnp-2011-wo international publication report a1.pdf 2018-08-10
30 1250-MUMNP-2011-FORM 3(21-5-2014).pdf 2018-08-10
30 1250-MUMNP-2011_EXAMREPORT.pdf 2018-08-10
31 1250-MUMNP-2011-FORM 3(15-2-2012).pdf 2018-08-10
31 1250-MUMNP-2011-ORIGINAL UNDER RULE 6 (1A)-22-05-2017.pdf 2017-05-22
32 1250-MUMNP-2011-FORM 3(12-8-2011).pdf 2018-08-10
32 Form 13 [15-05-2017(online)].pdf 2017-05-15
33 1250-mumnp-2011-form 2.pdf 2018-08-10
33 Form 26 [15-05-2017(online)].pdf 2017-05-15
34 Other Document [15-05-2017(online)].pdf 2017-05-15
35 1250-mumnp-2011-form 2(title page).pdf 2018-08-10
35 Abstract [03-06-2016(online)].pdf 2016-06-03
36 Correspondence [03-06-2016(online)].pdf 2016-06-03
36 1250-MUMNP-2011-FORM 18(10-9-2012).pdf 2018-08-10
37 1250-MUMNP-2011-FORM 13(14-2-2012).pdf 2018-08-10
37 Description(Complete) [03-06-2016(online)].pdf 2016-06-03
38 Examination Report Reply Recieved [03-06-2016(online)].pdf 2016-06-03
38 1250-mumnp-2011-form 1.pdf 2018-08-10
39 OTHERS [03-06-2016(online)].pdf 2016-06-03
39 1250-mumnp-2011-description(complete).pdf 2018-08-10
40 1250-mumnp-2011-correspondence.pdf 2018-08-10
40 1250-MUMNP-2011-ASSIGNMENT-(16-03-2016).pdf 2016-03-16
41 1250-MUMNP-2011-CORRESPONDENCE-(16-03-2016).pdf 2016-03-16
41 1250-MUMNP-2011-CORRESPONDENCE(8-8-2011).pdf 2018-08-10
42 1250-MUMNP-2011-CORRESPONDENCE(10-9-2012).pdf 2018-08-10
42 1250-MUMNP-2011-FORM 3-(25-04-2015).pdf 2015-04-25
43 1250-mumnp-2011-claims.pdf 2018-08-10
43 1250-MUMNP-2011-FORM 3(10-11-2014).pdf 2014-11-10
44 1250-MUMNP-2011-FORM 3(10-12-2013).pdf 2013-12-10