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WO2004046292A1 - Improved detergent composition - Google Patents

Improved detergent composition Download PDF

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Publication number
WO2004046292A1
WO2004046292A1 PCT/EP2003/012186 EP0312186W WO2004046292A1 WO 2004046292 A1 WO2004046292 A1 WO 2004046292A1 EP 0312186 W EP0312186 W EP 0312186W WO 2004046292 A1 WO2004046292 A1 WO 2004046292A1
Authority
WO
WIPO (PCT)
Prior art keywords
composition according
water
composition
surfactants
surfactant
Prior art date
Application number
PCT/EP2003/012186
Other languages
French (fr)
Inventor
Sudhir Achar
Anand Mahabal Shetty
Original Assignee
Unilever N.V.
Unilever Plc
Hindustan Lever Limited
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 N.V., Unilever Plc, Hindustan Lever Limited filed Critical Unilever N.V.
Priority to MXPA05004942A priority Critical patent/MXPA05004942A/en
Priority to DE60313899T priority patent/DE60313899T2/en
Priority to BR0315253-7A priority patent/BR0315253A/en
Priority to EP03769482A priority patent/EP1625195B1/en
Priority to AU2003278170A priority patent/AU2003278170A1/en
Publication of WO2004046292A1 publication Critical patent/WO2004046292A1/en

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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
    • C11D3/16Organic 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
    • C11D3/225Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin etherified, e.g. CMC
    • 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
    • C11D1/83Mixtures of non-ionic with anionic compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/12Water-insoluble compounds
    • C11D3/14Fillers; Abrasives ; Abrasive compositions; Suspending or absorbing agents not provided for in one single group of C11D3/12; Specific features concerning abrasives, e.g. granulometry or mixtures
    • 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
    • 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
    • C11D3/37Polymers
    • C11D3/3703Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3707Polyethers, e.g. polyalkyleneoxides
    • 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
    • C11D3/37Polymers
    • C11D3/3746Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3757(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions
    • 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
    • C11D3/37Polymers
    • C11D3/3746Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3757(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions
    • C11D3/3765(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions in liquid compositions
    • 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
    • C11D3/37Polymers
    • C11D3/3746Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3769(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines
    • 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
    • C11D3/37Polymers
    • C11D3/3788Graft polymers

Definitions

  • the invention relates to synergistic cleaning compositions, containing surfactants and swellable polymers, which are suited to the cleaning of hard surfaces.
  • Commercial hard surface cleaning compositions typically comprise one or more surfactants and a plurality of abrasive
  • abrasives used in these compositions include calcites and dolomites .
  • Hard surfaces within household are kitchenware, kitchen walls and floors, worktops and sinks, , bathrooms walls, floors and
  • the soil generally encountered on kitchenware and cooker tops is of two types i.e. the mobile or greasy soil and the tough or difficult to remove soil consisting of dried-on or cooked-on food.
  • the level of the surfactant in the cleaning compositions is upto about 20% and the rest is constituted of
  • Abrasives, builders and fillers form an important part of the formulation. It is necessary to add these ingredients to improve the spreadability of the surfactant active on to the cleaning surface especially in hand wash situations .
  • EP883670 (Unilever, 1998), discloses dishwashing gel compositions for machine wash that have high viscosity. They have a dual component structuring system comprising 0.2-2% of a cross-linked polycarboxylate and an azole.
  • the present invention provides a synergistic concentrated cleaning composition comprising one or more surfactants and one or more water swellable polymers that can absorb more than their weight of water.
  • the composition can be converted into a voluminous paste or thick liquid by the simple addition of water prior to use, to ensure the spreadability of the composition on a large number of surfaces to be cleaned.
  • the present invention thus provides a synergistic cleaning composition
  • a synergistic cleaning composition comprising a) 5-95% of one or more surfactants b) 5-95% of one or more of water swellable polymers that absorb more than their weight of water and
  • cleaning composition refers to compositions in the form of solid powders, tablets, pellets or noodles, or to pastes or gels, that can be converted into a product with enhanced volume by addition of water. The product so obtained can be more easily applied to or spread over the surface to be cleaned.
  • composition according to the invention will comprise one or more surfactants that are generally chosen from anionic, nonionic, cationic, or amphoteric surfactants. It is preferred that at least 10% of the total amount of surfactant in the composition consists of nonionic surfactant, more preferably at least 40% of total surfactant. It is preferred that the surfactant in the composition is from 5 to 50% more preferably 5 to 25 % by weight of the composition.
  • a suitable class of anionic surfactants are water-soluble salts of organic sulphuric acid mono-esters and sulphonic acids having in the molecular structure a branched or straight chain alkyl group containing 8-22 C atoms or an alkylaryl group containing 6-20 C atoms in the alkyl part.
  • anionic surfactants are water soluble salts of: - long chain (i.e. 8-22 C-atom) alcohol sulphates
  • PAS especially those obtained by sulphating the fatty alcohols produced from tallow or coconut oil or the synthetic alcohols derived from petroleum; - alkylbenzene-sulphonates, such as those in which the alkyl group contains from 6 to 20 carbon atoms; secondary alkanesulphonates .
  • alkylglyceryl ether sulphates especially of the ethers of fatty alcohols derived from tallow and coconut oil; fatty acid monoglyceride sulphates; sulphates of ethoxylated aliphatic alcohols containing 1-12 ethyleneoxy groups; alkylphenol ethylenoxy-ether sulphates with from 1 to 8 ethyleneoxy units per molecule and in which the alkyl groups contain from 4 to 14 carbon atoms; the reaction product of fatty acids esterified with isethionic acid and neutralised with alkali.
  • a suitable class of nonionic surfactants can be broadly described as compounds produced by the condensation of simple alkylene oxides, which are hydrophilic in nature, with an aliphatic or alkyl-aromatic hydrophobic compound having a reactive hydrogen atom.
  • the length of the hydrophilic or polyoxyalkylene chain which is attached to any particular hydrophobic group can be readily adjusted to yield a compound having the desired balance between hydrophilic and hydrophobic elements. This enables the choice of nonionic surfactants with the right HLB.
  • Particular examples include: the condensation products of aliphatic alcohols having from 8 to 22 carbon atoms in either straight or branched chain configuration with ethylene oxide, such as a coconut alcohol/ethylene oxide condensates having from 2 to 15 moles of ethylene oxide per mole of coconut alcohol; condensates of alkylphenols having C6-C15 alkyl groups with 5 to 25 moles of ethylene oxide per mole of alkylphenol; - condensates of the reaction product of ethylene-diamine and propylene oxide with ethylene oxide, the condensates containing from 40 to 80% of ethyleneoxy groups by weight and having a molecular weight of from 5,000 to 11,000.
  • alkyl polyglycosides which are condensation products of long chain aliphatic alcohols and saccharides
  • tertiary amine oxides of structure RRRNO where one R is an alkyl group of 8 to 20 carbon atoms and the other R's are each alkyl or hydroxyalkyl groups of 1 to 3 carbon atoms, e.g.
  • dimethyldodecylamine oxide dimethyldodecylamine oxide
  • tertiary phosphine oxides of structure RRRP0 where one R is an alkyl group of 8 to 20 carbon atoms and the other R's are each alkyl or hydroxyalkyl groups of 1 to 3 carbon atoms, for instance dimethyl-dodecylphosphine oxide
  • dialkyl sulphoxides of structure RRS0 where one R is an alkyl group of from 10 to 18 carbon atoms and the other is methyl or ethyl, for instance methyl-tetradecyl sulphoxide
  • fatty acid alkylolamides such as the ethanol amides
  • - alkylene oxide condensates of fatty acid alkylolamides
  • alkyl mercaptans alkyl mercaptans.
  • a specific group of surfactants are the tertiary amines obtained by condensation of ethylene and/or propylene oxide with long chain aliphatic amines.
  • the compounds behave like nonionic surfactants in alkaline medium and like cationic surfactants in acid medium.
  • amphoteric, cationic or zwitterionic surfactants in the compositions according to the invention.
  • Suitable amphoteric surfactant compounds that optionally can be employed are derivatives of aliphatic secondary and tertiary amines containing an alkyl group of 8 to 18 carbon atoms and an aliphatic radical, substituted by an anionic water-solubilizing group, for instance sodium 3-dodecylamino-propionate, sodium 3- dodecylaminopropane sulphonate and sodium N-2-hydroxydodecyl-N- methyltaurate .
  • Suitable cationic surfactants can be found among quaternary ammonium salts having one or two alkyl or aralkyl groups of from 8 to 20 carbon atoms and two or three small aliphatic (e.g. methyl) groups, for instance cetyltrimethylammonium bromide
  • Suitable zwitterionic surfactants can be found among derivatives of aliphatic quaternary ammonium, sulphonium and phosphonium compounds having an aliphatic group of from 8 to 18 carbon atoms and an aliphatic group substituted by an anionic water-solubilising group, for instance: 3- (N,N-dimethyl-N- hexadecylammonium) -propane-1-sulphonate betaine, 3- (dodecylmethyl-sulphonium) -propane-1-sulphonate betaine and 3- (cetylmethyl-phosphonium) -ethanesulphonate betaine.
  • Other well known betaines are the alkylamidopropyl betaines e.g. those wherein the alkylamido group is derived from coconut oil fatty acids.
  • surfactants are compounds commonly used as surface-active agents given in the well-known textbooks : “Surface Active Agents” Vol.l, by
  • the surfactant is a mixture of anionic and nonionic surfactants in a ratio in the range of 1:0.1 to 1:10 and more preferably between 1:0.1 and 1:1
  • the preferred water-swellable polymers are polyacrylic acids and polyacrylates, cross-linked acrylate polymers, guar gum and its derivatives, starch-acrylic grafted copolymers, hydrolysates of starch-acrylonitrile grafted copolymers, cross- linked polyoxyethylene, cross-linked carboxymethylcellulose, partially cross-linked water swellable polymers such as polyethylene oxide and polyacrylamide, isobutylene/maleic acid copolymers, etc.
  • the particularly preferred water swellable polymers are polyacrylic acids and the most preferred are cross linked polyacrylic acids partially neutralised to the sodium salts.
  • the water swellable polymers for the present invention are available as solids and liquids and the preferable forms are solid forms, such as particles, granules, pellets, flakes, short needles and the like. It is preferred that the water swellable polymer in the composition is from 5 to 75% more preferably 5 to 50 % by weight of the composition.
  • the surfactant to polymer ratio is preferably in the range of 1:0.1 to 0.1:1 and more preferably 1:0.4 to 0.4:1.
  • a particulate insoluble solid phase is an optional ingredient of the compositions according to the present invention.
  • the particulate phase comprises an abrasive which is insoluble in water.
  • the abrasive may be soluble to some extent and be present in such excess to water present in the composition when it is mixed with water prior to use, that the solubility of the abrasive in the aqueous phase is exceeded and consequently the abrasive exists in the solid phase in the swollen mixture.
  • the gel or paste forming capacity of the swellable polymers may be reduced in the presence of certain electrolytes.
  • certain electrolytes For example, calcium ions reduces the swellability of the cross linked polyacrylic acid which is a water swellable polymer.
  • Suitable abrasives can be selected from, particulate zeolites, calcites, dolomites, feldspar, silicas, silicates, other carbonates, aluminas, bicarbonates, borates, sulphates and polymeric materials such as polyethylene.
  • Preferred abrasives for use in general purpose cleaning compositions have a Moh hardness 2-6 although higher hardness abrasives can be employed for specialist applications.
  • Preferred average particle sizes for the abrasive fall in the range 0.5-400 microns, with values of around 5-200 microns being preferred.
  • compositions according to the invention can contain other ingredients which aid in their cleaning performance.
  • the composition can contain detergent builders such as nitrilotriacetates, polycarboxylates, citrates, dicarboxylic acids, water-soluble phosphates (such as polyphosphates, mixtures of ortho- and pyrophosphates) , zeolites and mixtures thereof.
  • Compositions according to the invention can also contain, in addition to the ingredients already mentioned, various other optional ingredients such as solvents, colourants, whiteners, optical brighteners, soil suspending agents, detersive enzymes, compatible bleaching agents (particularly hypohalites) , and preservatives.
  • Inorganic particulars and other optional ingredients can be present in a amuont of up tp 90% of the composition.
  • synergistic cleaning composition comprising:
  • synergistic cleaning composition comprising:
  • compositions as outlined in Table 1 were prepared by mixing of the surfactant and the polymer. The products were obtained as a powdery mass. 50g of water was added to each of these products and allowed to stand for 1-2 minutes. The visual appearance of the products after addition of water and the gel volume obtained are also presented in the table 1.
  • Measurement of Gel volume (ml) after addition of excess water The paste/thick liquids formed in Example 1-6 above were transferred to separate 250 mL graduated measuring cylinders and the volume was made up to 250mL by adding water. The contents of the cylinders were stirred for a minute and were allowed to settle overnight and observed. The contents of the cylinders separated into two phases (in Examples 1,2,3 and 6).
  • the gel formed by the swellable polymer settled in the bottom while the water layer was at the top.
  • the volume of the gel layer was measured.
  • the volume of the gels indicates the gel forming capacity of the swellable polymer in presence of the surfactants. It is inferred that the more the gel volume, the less is the negative impact of the surfactant on the the swellable polymer.
  • Measurement of cleaning efficacy lg of the gel formed by adding 100 g water on to 7.5g powder was taken as a swipe using an implement and a soiled plate was cleaned. Different parameters of cleaning and in-use properties were determined during the cleaning operation. Based on an overall benefit the cleaning efficacy was graded on a scale of 1-5 where '1' refers to 'poor' and '5' refers to 'good' performance.

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Engineering & Computer Science (AREA)
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Abstract

The invention relates to synergistic concentrated cleaning composition comprising one or more surfactants and one or more water swellable polymers that can absorb more than their weight of water. The composition can be converted into a voluminous paste or thick liquid by the simple addition of water prior to use, to ensure the spreadability of the composition on a large number of surfaces to be cleaned.

Description

Improved. Detergent Composition
Technical field
5
The invention relates to synergistic cleaning compositions, containing surfactants and swellable polymers, which are suited to the cleaning of hard surfaces.
10
Background Art
Commercial hard surface cleaning compositions typically comprise one or more surfactants and a plurality of abrasive
15 particles dispersed therein. Combinations of surfactants, together with electrolytes, are often used to form a suspending system for the abrasives, as is well known in the art. Various forms of cleaning compositions are available that are in the form of liquids, pastes, gels, powders and bars. Typical
20. abrasives used in these compositions include calcites and dolomites .
Hard surfaces within household are kitchenware, kitchen walls and floors, worktops and sinks, , bathrooms walls, floors and
25 fixtures, other floors, etc. and one encounters different types of soil on these surfaces. The soil generally encountered on kitchenware and cooker tops is of two types i.e. the mobile or greasy soil and the tough or difficult to remove soil consisting of dried-on or cooked-on food. The problem of
30 removing this soil becomes more pronounced when the tough soil builds on over a period of time and it requires considerable effort to clean.
In general the level of the surfactant in the cleaning compositions is upto about 20% and the rest is constituted of
35 other ingredients. Abrasives, builders and fillers form an important part of the formulation. It is necessary to add these ingredients to improve the spreadability of the surfactant active on to the cleaning surface especially in hand wash situations .
Polymers have been used in cleaning compositions for various benefits such as structuring and soil release functions. EP883670 (Unilever, 1998), discloses dishwashing gel compositions for machine wash that have high viscosity. They have a dual component structuring system comprising 0.2-2% of a cross-linked polycarboxylate and an azole.
Adding a large amount of water along with abrasives, builders, and fillers adds to the bulk of the product and hence increases the cost and difficulty of transportation from the place of manufacture to the point of use.
Thus, there is a need for a concentrated cleaning composition that can be converted to a ready-to-use product by the consumer by adding water. This concentrated composition would save on the cost of transport and packaging compared to a dilute composition.
Brief description of the invention
The present invention provides a synergistic concentrated cleaning composition comprising one or more surfactants and one or more water swellable polymers that can absorb more than their weight of water. The composition can be converted into a voluminous paste or thick liquid by the simple addition of water prior to use, to ensure the spreadability of the composition on a large number of surfaces to be cleaned. Detailed Description
All parts and precentages mentioned herein are by weight of the composition unless otherwise specified.
The present invention thus provides a synergistic cleaning composition comprising a) 5-95% of one or more surfactants b) 5-95% of one or more of water swellable polymers that absorb more than their weight of water and
In the context of the present invention, the expression "cleaning composition" refers to compositions in the form of solid powders, tablets, pellets or noodles, or to pastes or gels, that can be converted into a product with enhanced volume by addition of water. The product so obtained can be more easily applied to or spread over the surface to be cleaned.
Surfactants
The composition according to the invention will comprise one or more surfactants that are generally chosen from anionic, nonionic, cationic, or amphoteric surfactants. It is preferred that at least 10% of the total amount of surfactant in the composition consists of nonionic surfactant, more preferably at least 40% of total surfactant. It is preferred that the surfactant in the composition is from 5 to 50% more preferably 5 to 25 % by weight of the composition.
A suitable class of anionic surfactants are water-soluble salts of organic sulphuric acid mono-esters and sulphonic acids having in the molecular structure a branched or straight chain alkyl group containing 8-22 C atoms or an alkylaryl group containing 6-20 C atoms in the alkyl part.
Examples of such anionic surfactants are water soluble salts of: - long chain (i.e. 8-22 C-atom) alcohol sulphates
(hereinafter referred to as PAS) , especially those obtained by sulphating the fatty alcohols produced from tallow or coconut oil or the synthetic alcohols derived from petroleum; - alkylbenzene-sulphonates, such as those in which the alkyl group contains from 6 to 20 carbon atoms; secondary alkanesulphonates . Also suitable are the salts of: alkylglyceryl ether sulphates, especially of the ethers of fatty alcohols derived from tallow and coconut oil; fatty acid monoglyceride sulphates; sulphates of ethoxylated aliphatic alcohols containing 1-12 ethyleneoxy groups; alkylphenol ethylenoxy-ether sulphates with from 1 to 8 ethyleneoxy units per molecule and in which the alkyl groups contain from 4 to 14 carbon atoms; the reaction product of fatty acids esterified with isethionic acid and neutralised with alkali.
A suitable class of nonionic surfactants can be broadly described as compounds produced by the condensation of simple alkylene oxides, which are hydrophilic in nature, with an aliphatic or alkyl-aromatic hydrophobic compound having a reactive hydrogen atom. The length of the hydrophilic or polyoxyalkylene chain which is attached to any particular hydrophobic group can be readily adjusted to yield a compound having the desired balance between hydrophilic and hydrophobic elements. This enables the choice of nonionic surfactants with the right HLB. Particular examples include: the condensation products of aliphatic alcohols having from 8 to 22 carbon atoms in either straight or branched chain configuration with ethylene oxide, such as a coconut alcohol/ethylene oxide condensates having from 2 to 15 moles of ethylene oxide per mole of coconut alcohol; condensates of alkylphenols having C6-C15 alkyl groups with 5 to 25 moles of ethylene oxide per mole of alkylphenol; - condensates of the reaction product of ethylene-diamine and propylene oxide with ethylene oxide, the condensates containing from 40 to 80% of ethyleneoxy groups by weight and having a molecular weight of from 5,000 to 11,000.
Other classes of nonionic surfactants are: alkyl polyglycosides, which are condensation products of long chain aliphatic alcohols and saccharides; tertiary amine oxides of structure RRRNO, where one R is an alkyl group of 8 to 20 carbon atoms and the other R's are each alkyl or hydroxyalkyl groups of 1 to 3 carbon atoms, e.g. dimethyldodecylamine oxide; tertiary phosphine oxides of structure RRRP0, where one R is an alkyl group of 8 to 20 carbon atoms and the other R's are each alkyl or hydroxyalkyl groups of 1 to 3 carbon atoms, for instance dimethyl-dodecylphosphine oxide; dialkyl sulphoxides of structure RRS0 where one R is an alkyl group of from 10 to 18 carbon atoms and the other is methyl or ethyl, for instance methyl-tetradecyl sulphoxide; fatty acid alkylolamides, such as the ethanol amides; - alkylene oxide condensates of fatty acid alkylolamides; alkyl mercaptans. A specific group of surfactants are the tertiary amines obtained by condensation of ethylene and/or propylene oxide with long chain aliphatic amines. The compounds behave like nonionic surfactants in alkaline medium and like cationic surfactants in acid medium.
It is possible optionally to include amphoteric, cationic or zwitterionic surfactants in the compositions according to the invention.
Suitable amphoteric surfactant compounds that optionally can be employed are derivatives of aliphatic secondary and tertiary amines containing an alkyl group of 8 to 18 carbon atoms and an aliphatic radical, substituted by an anionic water-solubilizing group, for instance sodium 3-dodecylamino-propionate, sodium 3- dodecylaminopropane sulphonate and sodium N-2-hydroxydodecyl-N- methyltaurate .
Examples of suitable cationic surfactants can be found among quaternary ammonium salts having one or two alkyl or aralkyl groups of from 8 to 20 carbon atoms and two or three small aliphatic (e.g. methyl) groups, for instance cetyltrimethylammonium bromide
Examples of suitable zwitterionic surfactants can be found among derivatives of aliphatic quaternary ammonium, sulphonium and phosphonium compounds having an aliphatic group of from 8 to 18 carbon atoms and an aliphatic group substituted by an anionic water-solubilising group, for instance: 3- (N,N-dimethyl-N- hexadecylammonium) -propane-1-sulphonate betaine, 3- (dodecylmethyl-sulphonium) -propane-1-sulphonate betaine and 3- (cetylmethyl-phosphonium) -ethanesulphonate betaine. Other well known betaines are the alkylamidopropyl betaines e.g. those wherein the alkylamido group is derived from coconut oil fatty acids.
Further examples of suitable surfactants are compounds commonly used as surface-active agents given in the well-known textbooks : "Surface Active Agents" Vol.l, by
Schwartz & Perry, Interscience 1949; "Surface Active Agents" Vol.2 by Schwartz, Perry & Berch, Interscience 1958; the current edition of "McCutcheon' s Emulsifiers and Detergents" published by Manufacturing Confectioners Company; "Tenside- Taschenbuch", H. Stache, 2nd Edn., Carl Hauser Verlag, 1981.
It is particularly preferred that the surfactant is a mixture of anionic and nonionic surfactants in a ratio in the range of 1:0.1 to 1:10 and more preferably between 1:0.1 and 1:1
Swellable Polymers:
The preferred water-swellable polymers are polyacrylic acids and polyacrylates, cross-linked acrylate polymers, guar gum and its derivatives, starch-acrylic grafted copolymers, hydrolysates of starch-acrylonitrile grafted copolymers, cross- linked polyoxyethylene, cross-linked carboxymethylcellulose, partially cross-linked water swellable polymers such as polyethylene oxide and polyacrylamide, isobutylene/maleic acid copolymers, etc. The particularly preferred water swellable polymers are polyacrylic acids and the most preferred are cross linked polyacrylic acids partially neutralised to the sodium salts. The water swellable polymers for the present invention are available as solids and liquids and the preferable forms are solid forms, such as particles, granules, pellets, flakes, short needles and the like. It is preferred that the water swellable polymer in the composition is from 5 to 75% more preferably 5 to 50 % by weight of the composition.
The surfactant to polymer ratio is preferably in the range of 1:0.1 to 0.1:1 and more preferably 1:0.4 to 0.4:1.
Optional Ingredients
Inorganic particulates: A particulate insoluble solid phase is an optional ingredient of the compositions according to the present invention.
Preferably, the particulate phase comprises an abrasive which is insoluble in water. In the alternative, the abrasive may be soluble to some extent and be present in such excess to water present in the composition when it is mixed with water prior to use, that the solubility of the abrasive in the aqueous phase is exceeded and consequently the abrasive exists in the solid phase in the swollen mixture.
The gel or paste forming capacity of the swellable polymers may be reduced in the presence of certain electrolytes. For example, calcium ions reduces the swellability of the cross linked polyacrylic acid which is a water swellable polymer. Hence while choosing the abrasives and inorganic particulates, care must be exercised to avoid such materials. If their use is absolutely necessary, then they have to be used in minimum quantities .
Suitable abrasives can be selected from, particulate zeolites, calcites, dolomites, feldspar, silicas, silicates, other carbonates, aluminas, bicarbonates, borates, sulphates and polymeric materials such as polyethylene. Preferred abrasives for use in general purpose cleaning compositions have a Moh hardness 2-6 although higher hardness abrasives can be employed for specialist applications.
Preferred average particle sizes for the abrasive fall in the range 0.5-400 microns, with values of around 5-200 microns being preferred.
Other Optional ingredients
The composition according to the invention can contain other ingredients which aid in their cleaning performance. For example, the composition can contain detergent builders such as nitrilotriacetates, polycarboxylates, citrates, dicarboxylic acids, water-soluble phosphates (such as polyphosphates, mixtures of ortho- and pyrophosphates) , zeolites and mixtures thereof. Compositions according to the invention can also contain, in addition to the ingredients already mentioned, various other optional ingredients such as solvents, colourants, whiteners, optical brighteners, soil suspending agents, detersive enzymes, compatible bleaching agents (particularly hypohalites) , and preservatives.
Inorganic particulars and other optional ingredients can be present in a amuont of up tp 90% of the composition.
Thus according to a preferred aspect of the present invention there is provided a synergistic cleaning composition comprising:
a) 5-50% of one or more surfactants that has at least 10% of the total surfactant weight as nonionic surfactant b) 5-75% of one or more of water swellable polymer that absorbs more than its weight of water and c) optionally up to 90% by weight, of inorganic particulates and other conventional ingredients.
Thus according to a more preferred aspect of the present invention there is provided a synergistic cleaning composition comprising :
a) 5-25% of one or more surfactant that has at least 40% of the weight of the total surfactant as nonionic surfactant b) 5-50% by weight. of one or more of water swellable polymer that absorbs more than its weight of water and 10-90% by weight inorganic particulates and other conventional ingredients.
The invention will now be illustrated with respect to the following non-limiting examples .
Examples :
i. Effect of the polymer-surfactant interaction on gel formation: Compositions as outlined in Table 1 were prepared by mixing of the surfactant and the polymer. The products were obtained as a powdery mass. 50g of water was added to each of these products and allowed to stand for 1-2 minutes. The visual appearance of the products after addition of water and the gel volume obtained are also presented in the table 1. Measurement of Gel volume (ml) after addition of excess water: The paste/thick liquids formed in Example 1-6 above were transferred to separate 250 mL graduated measuring cylinders and the volume was made up to 250mL by adding water. The contents of the cylinders were stirred for a minute and were allowed to settle overnight and observed. The contents of the cylinders separated into two phases (in Examples 1,2,3 and 6). The gel formed by the swellable polymer settled in the bottom while the water layer was at the top. The volume of the gel layer was measured. The volume of the gels (in presence of excess amount of water) indicates the gel forming capacity of the swellable polymer in presence of the surfactants. It is inferred that the more the gel volume, the less is the negative impact of the surfactant on the the swellable polymer.
Table 1
Figure imgf000012_0001
The data presented in table 1 show that the polymer is essential for forming a gel and in presence of nonionic surfactants the polymer forms a good solid like gel. This shows that the choice of the surfactant is important in determining the gel strength and volume which in turn determines the consistency of the paste formed.
ii. Effect of the nature of the surfactant on gel formation: Anionic surfactant and nonionic surfactant in different ratios in compositions described in table 2 were studied to determine the effect on gel formation. The product was mixed with water and the nature of the gel was studied. Measurement of Gel volume (mL) after addition of excess water was determined by the procedure described above. The performance was also assessed by considering the cleaning efficiency.
Measurement of cleaning efficacy: lg of the gel formed by adding 100 g water on to 7.5g powder was taken as a swipe using an implement and a soiled plate was cleaned. Different parameters of cleaning and in-use properties were determined during the cleaning operation. Based on an overall benefit the cleaning efficacy was graded on a scale of 1-5 where '1' refers to 'poor' and '5' refers to 'good' performance.
Table 2
Figure imgf000014_0001
The data presented in Table 2 show that the polymer is essential for obtaining a consistent gel but performs poorly with regard to cleaning (Example 9) . When the surfactant alone is present in the absence of the polymer no gel is obtained and the cleaning efficacy is reduced (examples 10 and 11) because the polymer aids in the spreadability of the active. The performance of the compositions as in Examples 7, 8,12 and 13, in terms of gel formation and cleaning efficacy indicate that the right combination of the surfactant and the polymer is important in obtaining a composition that has both optimal cleaning and good gel strength.

Claims

1. A synergistic cleaning composition comprising surfactants and polymer wherein: a) one or more surfactants are present in an amount of 5- 95% , b) one or more water-swellable polymers that absorb more than their weight of water are present in an amount of 5-95%
2. A composition according to claim 1 wherein the water- swellable polymer is chosen from the group consisting of polyacrylic acids, polyacrylates, cross linked acrylate polymers, guar gum and its derivatives, starch-acrylic grafted copolymers, hydrolysates of starch-acrylonitrile grafted copolymers, cross linked polyoxyethylene, cross linked carboxymethylcellulose, partially cross linked water swellable polymers such as polyethylene oxide and polyacrylamide, isobutylene, and aleic acid copolymer.
3. A composition according to claim 2 wherein the water- swellable polymer is chosen from polyacrylic acids or partially neutralised sodium salts of cross linked polyacrylic acids.
4. A composition according to any of claims 1 to 3 wherein the water-swellable polymer is from 5 to 75% of the composition.
5. A composition according to claim 4 wherein the water- swellable polymer is from 5 to 50% of the composition.
6. A composition according to any of claims 1 to 5 wherein the surfactants are chosen from anionic and/or nonionic surfactants .
7. A composition according to any of claims 1 or 6 wherein the nonionic surfactant is at least 10% by weight of the total surfactants
8. A composition according to any of claims 1 to 7 wherein the nonionic surfactant is at least 40% by weight of the total surfactant .
9. A composition according to any of claims 6 to 8 wherein the weight ratio of the anionic to nonionic surfactants is in the range of 0.1:1 to 1:0.1
10. A composition according to claim 9 wherein the weight ratio of the anionic to nonionic surfactant is 1:1.
11. A composition according to any of claims 1 to 10 wherein the composition comprises total surfactants in the range of 5 to 50% of the composition.
12. A composition according to claim 11 wherein the composition comprises surfactants in the range of 5 to 25% of the composition.
13. A composition according to any of claims 1 to 12 wherein the weight ratio of the surfactant to the water swellable polymer is in the range of 1: 0.1 to 0.1 :1.
14. A composition according to claim 13 wheerin the weight ratio of the surfactant to the water swellable polymer is in the range of 1 : 0.4 to 0.4 : 1.
15. A composition according to any of claims 1 to 14 wherein the composition is in the form of solid powders, tablets, pellets, noodles, pastes or gels.
16. A composition according to any of claims 1 to 15 wherein the water-swellable polymer is in the form of solid.
17. A composition according to claim 16 wherein the water- swellable polymer is in the form of particles, granules, pellets, flakes, or short needles.
18. A composition according to any one of claims 1-17 wherein the composition additionally comprises up to 90% of inorganic particulates and other conventional ingredients.
19. A composition according to any of claims 1 to 18 wherein the composition includes 10 to 90% of inorganic particulate phase.
20. A composition according to claims 18 or 19 wherein the particulate phase is a water-insoluble or partly soluble abrasive.
PCT/EP2003/012186 2002-11-15 2003-10-21 Improved detergent composition WO2004046292A1 (en)

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BR0315253-7A BR0315253A (en) 2002-11-15 2003-10-21 Synergistically cleaning composition
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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009000958A1 (en) * 2007-06-26 2008-12-31 Universidad De Granada Detergents for hard surfaces
GB2481704A (en) * 2010-07-01 2012-01-04 Amcrol Ltd Polyacrylamide and starch cleaning material
WO2016096328A1 (en) 2014-12-18 2016-06-23 Unilever N.V. Powder composition for hard surface cleaning
US11168286B2 (en) 2016-08-24 2021-11-09 Reckitt Benckiser Finish B.V. Method of making a detergent composition

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Publication number Priority date Publication date Assignee Title
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Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998055583A1 (en) * 1997-06-06 1998-12-10 Unilever Plc Cleaning compositions
WO2000022091A1 (en) * 1998-10-09 2000-04-20 The Procter & Gamble Company Detergent compositions
WO2000042143A1 (en) * 1999-01-15 2000-07-20 Unilever Plc Detergent composition
EP1074608A1 (en) * 1999-08-02 2001-02-07 Robert McBride Ltd Detergent tablets
WO2001021756A1 (en) * 1999-09-23 2001-03-29 Unilever N.V. Cleaning compositions
US20020035049A1 (en) * 1997-02-20 2002-03-21 Susheel Kumar Suri Toilet cleaning block
EP1219700A1 (en) * 2000-12-28 2002-07-03 Unilever Plc Cleaning compositions
WO2002070574A2 (en) * 2001-03-02 2002-09-12 Unilever Plc Soil release polymers and laundry detergent compositions containing them

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020035049A1 (en) * 1997-02-20 2002-03-21 Susheel Kumar Suri Toilet cleaning block
WO1998055583A1 (en) * 1997-06-06 1998-12-10 Unilever Plc Cleaning compositions
WO2000022091A1 (en) * 1998-10-09 2000-04-20 The Procter & Gamble Company Detergent compositions
WO2000042143A1 (en) * 1999-01-15 2000-07-20 Unilever Plc Detergent composition
EP1074608A1 (en) * 1999-08-02 2001-02-07 Robert McBride Ltd Detergent tablets
WO2001021756A1 (en) * 1999-09-23 2001-03-29 Unilever N.V. Cleaning compositions
EP1219700A1 (en) * 2000-12-28 2002-07-03 Unilever Plc Cleaning compositions
WO2002070574A2 (en) * 2001-03-02 2002-09-12 Unilever Plc Soil release polymers and laundry detergent compositions containing them

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009000958A1 (en) * 2007-06-26 2008-12-31 Universidad De Granada Detergents for hard surfaces
ES2316286A1 (en) * 2007-06-26 2009-04-01 Universidad De Granada Detergents for hard surfaces
GB2481704A (en) * 2010-07-01 2012-01-04 Amcrol Ltd Polyacrylamide and starch cleaning material
GB2481704B (en) * 2010-07-01 2015-04-22 Amcrol Ltd Cured Polyacrylamide and Starch Cleaning Material
WO2016096328A1 (en) 2014-12-18 2016-06-23 Unilever N.V. Powder composition for hard surface cleaning
US11168286B2 (en) 2016-08-24 2021-11-09 Reckitt Benckiser Finish B.V. Method of making a detergent composition
US11643619B2 (en) 2016-08-24 2023-05-09 Reckitt Benckiser Finish B.V. Method of making a detergent composition

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