WO2004018603A1 - Detergent compositions - Google Patents

Detergent compositions Download PDF

Info

Publication number
WO2004018603A1
WO2004018603A1 PCT/EP2003/007754 EP0307754W WO2004018603A1 WO 2004018603 A1 WO2004018603 A1 WO 2004018603A1 EP 0307754 W EP0307754 W EP 0307754W WO 2004018603 A1 WO2004018603 A1 WO 2004018603A1
Authority
WO
WIPO (PCT)
Prior art keywords
detergent composition
laundry detergent
polyvinyl pyrrolidone
detergency
pvp
Prior art date
Application number
PCT/EP2003/007754
Other languages
French (fr)
Inventor
Donna Macnab
Original Assignee
Unilever Plc
Unilever Nv
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=9942091&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO2004018603(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Unilever Plc, Unilever Nv, Hindustan Lever Limited filed Critical Unilever Plc
Priority to DE60305927T priority Critical patent/DE60305927T2/en
Priority to BR0312731-1A priority patent/BR0312731A/en
Priority to AU2003246709A priority patent/AU2003246709A1/en
Priority to EP03792209A priority patent/EP1527155B2/en
Publication of WO2004018603A1 publication Critical patent/WO2004018603A1/en

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
    • C11D3/16Organic 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
    • C11D3/3776Heterocyclic compounds, e.g. lactam
    • 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
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/22Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds

Definitions

  • the present invention relates to laundry detergent compositions containing polyvinyl pyrrolidone.
  • the compositions exhibit improved detergency on oily soils.
  • Polyvinyl pyrrolidone and some related polymers are known ingredients of laundry detergent compositions, providing the benefit of reduced dye transfer between fabrics in a mixed load.
  • Laundry detergent compositions containing polyvinyl pyrrolidone as a dye transfer inhibitor are disclosed, for example, in WO 92 18597A, WO 94 03567A, WO 95 03390A, WO 95 17496A, WO 95 27028A and WO 95 34627A (Procter 5-
  • GB 1 354 498 discloses laundry detergent compositions containing vinyl pyrrolidone/vinyl acetate copolymers as antiredeposition agents. Polyvinyl pyrrolidone itself is stated to be ineffective. It has now been discovered that polyvinyl pyrrolidone is also effective to enhance oily soil detergency, especially in detergent compositions containing anionic surfactants, more especially alk lbenzene sulphonate.
  • the present invention provides the use of polyvinyl pyrrolidone in a laundry detergent composition comprising an organic surfactant and optionally a detergency builder to improve the oily soil detergency of the composition.
  • the polyvinyl pyrrolidone (hereinafter PVP) preferably has a molecular weight within the range of from 10 000 to 100 000, more preferably from 25 000 to 75 000.
  • PVP is commercially available, for example, from BASF as the Luviskol (Trade Mark) K series (powders and solutions of various concentrations) and Sokalan (Trade Mark) HP50 (powder) , and from International Specialty Products (ISP) as the ISP-K series.
  • the laundry detergent composition is a laundry detergent composition
  • the PVP is present in an amount sufficient to enhance oily soil detergency.
  • the PVP is present in an amount of from from 0.5 to 3 wt%, preferably from 1 to
  • the detergent composition may suitably comprise:
  • the organic surfactant is the organic surfactant
  • the detergent composition in accordance with the invention may contain any organic surfactants (detergent-active compounds) suitable for incorporation into laundry detergent compositions .
  • Detergent-active compounds may be chosen from soap and non-soap anionic, cationic, nonionic, amphoteric and zwitterionic detergent-active compounds, and mixtures thereof.
  • Many suitable detergent-active compounds are available and are fully described in the literature, for example, in "Surface-Active Agents and Detergents", Volumes I and II, by Schwartz, Perry and Berch.
  • the preferred detergent-active compounds that can be used are soaps and synthetic non-soap anionic and nonionic compounds.
  • the total amount of surfactant present is suitably within the range of from 5 to 60 wt%, preferably from 5 to 40 wt%.
  • Anionic surfactants are well-known to those skilled in the art.
  • alkylbenzene sulphonates particularly linear alkylbenzene sulphonates having an alkyl chain length of Cs-Cis
  • primary and secondary alkylsulphates particularly C 8 -C 20 primary alkyl sulphates
  • alkyl ether sulphates particularly C 8 -C 20 primary alkyl sulphates
  • alkyl ether sulphates particularly C 8 -C 20 primary alkyl sulphates
  • alkyl ether sulphates particularly olefin sulphonates
  • alkyl xylene sulphonates dialkyl sulphosuccinates
  • fatty acid ester sulphonates are generally preferred.
  • Nonionic surfactants that may be used include the primary and secondary alcohol ethoxylates, especially the Ce-C 2 o aliphatic alcohols ethoxylated with an average of from 1 to 20 moles of ethylene oxide per mole of alcohol, and more especially the C 0 -C 5 primary and secondary aliphatic alcohols ethoxylated with an average of from 1 to 10 moles of ethylene oxide per mole of alcohol.
  • Non-ethoxylated nonionic surfactants include alkylpolyglycosides, glycerol monoethers, and polyhydroxyamides (glucamide) .
  • Cationic surfactants that may be used include quaternary ammonium salts, quaternary ammonium salts, and others.
  • R 1 R 2 R 3 R 4 N X wherein the R groups are long or short hydrocarbyl chains, typically alkyl, hydroxyalkyl or ethoxylated alkyl groups, and X is a solubilising anion (for example, compounds in which Ri is a c 8 - c 22 alkyl group, preferably a Cs-Cio or C 12 -C 14 alkyl group, R 2 is a methyl group, and R 3 and R 4 , which may be the same or different, are methyl or hydroxyethyl groups) ; and cationic esters (for example, choline esters) .
  • R groups are long or short hydrocarbyl chains, typically alkyl, hydroxyalkyl or ethoxylated alkyl groups
  • X is a solubilising anion (for example, compounds in which Ri is a c 8 - c 22 alkyl group, preferably a Cs-Cio or C 12 -C 14 alky
  • Amphoteric surfactants and/or zwitterionic surfactants may also be present.
  • Preferred amphoteric surfactants are amine oxides. These are materials of the general formula RlR 2 R3N ⁇ 0
  • R is typically a Cs-Cis alkyl group, for example, Ci 2 ⁇ i alkyl
  • R 2 and R 3 which may be the same or different, are C 1 -C 3 alkyl or hydroxyalkyl groups, for example, methyl groups.
  • the most preferred amine oxide is coco dimethylamine oxide.
  • Preferred zwitterionic surfactants are betaines, and especially amidobetaines .
  • Preferred betaines are C 8 -C 3 alkyl amidoalkylbetaines, for example, coco amidopropyl betaine (CAPB) .
  • the composition comprises a sulphonate anionic surfactant.
  • the sulphonate anionic surfactant comprises linear alkylbenzene sulphonate (LAS) .
  • the compositions contains from 3 to 30 wt%, more preferably from 10 to 25 wt%, of LAS.
  • the optional detergency builder is also observed.
  • the detergent compositions in accordance with the invention also contain one or more detergency builders .
  • the total amount of detergency builder in the compositions may suitably range from 5 to 80 wt%, preferably from 10 to 60 wt%.
  • Preferred builders are alkali metal aluminosilicates, more especially crystalline alkali metal aluminosilicates (zeolites) , preferably in sodium salt form.
  • Zeolite builders may suitably be present in a total amount of from 5 to 60 wt%, preferably from 10 to 50 wt%.
  • the zeolites may be supplemented by other inorganic builders, for example, amorphous aluminosilicates, or layered silicates such as SKS-6 ex Clariant .
  • the zeolites may be supplemented by organic builders, for example, polycarboxylate polymers such as polyacrylates and acrylic/maleic copolymers; monomeric polycarboxylates such as citrates, gluconates, oxydisuccinates, glycerol mono-, di- and trisuccinates, carboxymethyloxysuccinates, carboxymethyloxymalonates, dipicolinates, hydroxyethyliminodiacetates, alkyl- and alkenylmalonates and succinates; and sulphonated fatty acid salts.
  • the compositions in accordance with the invention may contain phosphate builders, for example, sodium tripolyphosphate .
  • organic builders are citrates, suitably used in amounts of from 1 to 30 wt%, preferably from 2 to 15 wt%; and acrylic polymers, more especially acrylic/maleic copolymers, suitably used in amounts of from 0.5 to 15 wt%, preferably from 1 to 10 wt%.
  • Builders both inorganic and organic, are preferably present in alkali metal salt, especially sodium salt, form.
  • the detergency builder which is present in an amount of from 5 to 80 wt%, preferably from 10 to 60 wt%, is selected from sodium tripolyphosphate, zeolites, sodium carbonate and mixtures thereof .
  • Detergent compositions in accordance with the invention may also suitably contain a bleach system.
  • a bleach system Preferably this will include a peroxy bleach compound, for example, an inorganic persalt or an organic peroxyacid, capable of yielding hydrogen peroxide in aqueous solution.
  • Preferred inorganic persalts are sodium perborate monohydrate and tetrahydrate, and sodium percarbonate, the latter being especially preferred.
  • the sodium percarbonate may have a protective coating against destabilisation by moisture.
  • the peroxy bleach compound is suitably present in an amount of from 5 to 35 wt%, preferably from 10 to 25 wt%.
  • the peroxy bleach compound may be used in conjunction with a bleach activator (bleach precursor) to improve bleaching action at low wash temperatures.
  • the bleach precursor is suitably present in an amount of from 1 to 8 wt%, preferably from 2 to 5 wt%.
  • Preferred bleach precursors are peroxycarboxylic acid precursors, more especially peracetic acid precursors and peroxybenzoic acid precursors; and peroxycarbonic acid precursors.
  • An especially preferred bleach precursor suitable for use in the present invention is N,N,N' ,N' -tetracetyl ethylenediamine (TAED) .
  • a bleach stabiliser may also be present.
  • Suitable bleach stabilisers include ethylenediamine tetraacetate (EDTA) , diethylenetriamine pentaacetate (DTPA) , ethylenediamine disuccinate (EDDS) , and the polyphosphonates such as the Dequests (Trade Mark) , ethylenediamine tetramethylene phosphonate (EDTMP) and diethylenetriamine pentamethylene phosphate (DETPMP) .
  • compositions in accordance with the invention may contain alkali metal, preferably sodium, carbonate, in order to increase detergency and ease processing.
  • Sodium carbonate may suitably be present in amounts ranging from 1 to 60 wt%, preferably from 2 to 40 wt%.
  • sodium silicate may also be present.
  • the amount of sodium silicate may suitably range from 0.1 to 5 wt%.
  • Sodium silicate, as previously indicated, is preferably introduced via the second base granule . Powder flow may be improved by the incorporation of a small amount of a powder structurant .
  • powder structurants examples include, for example, fatty acids (or fatty acid soaps) , sugars, acrylate or acrylate/maleate polymers, sodium silicate, and dicarboxylic acids (for example, Sokalan (Trade Mark) DCS ex BASF) .
  • fatty acids or fatty acid soaps
  • sugars for example, acrylate or acrylate/maleate polymers
  • sodium silicate for example, sodium silicate
  • dicarboxylic acids for example, Sokalan (Trade Mark) DCS ex BASF
  • fatty acid soap suitably present in an amount of from 1 to 5 wt%.
  • antiredeposition agents such as cellulosic polymers; soil release agents; anti-dye-transfer agents; fluorescers; inorganic salts such as sodium sulphate; enzymes
  • compositions in accordance with the invention may be of any suitable physical form, for example, particulates (powders, granules, tablets), liquids, pastes, gels or bars.
  • the detergent composition is in particulate form.
  • Powders of low to moderate bulk density may be prepared by spray-drying a slurry, and optionally postdosing (dry- mixing) further ingredients.
  • “Concentrated” or “compact” powders may be prepared by mixing and granulating processes, for example, using a high-speed mixer/granulator, or other non-tower processes.
  • Tablets may be prepared by compacting powders, especially "concentrated” powders.
  • liquid detergent compositions which may be prepared by admixing the essential and optional ingredients in any desired order to provide compositions containing the ingredients in the requisite concentrations.
  • the PVP may be incorporated at any suitable stage in the manufacture of the compositions in accordance with the invention.
  • PVP is commercially available both in solution form and in solid form.
  • PVP in powder or solution preferably aqueous
  • PVP powder or solution may be easily introduced into mixing and granulating apparatus, either alone or in admixture with other solid or liquid ingredients as appropriate .
  • wash liquors containing 1 g/litre or 2.5 g/litre of a notional detergent composition (the "product") containing linear alkylbenzene sulphonate (LAS) and sodium carbonate were prepared to the following general formulation:
  • the PVP samples used were as follows
  • Detergency on white cotton cloth soiled with dirty motor oil was assessed using a high throughput small scale wash method .
  • the wash was carried out in water of 20 (French) hardness (Ca:Mg 2:1), at a temperature of 20 C for 20 minutes .
  • Whiteness before and after the wash was determined using the technique of colour change by image analysis using a greyness scale.
  • the results are analogous to reflectance changes at 460 nm as measured by a reflectance spectrophotometer and are expressed as ⁇ R and ⁇ R.
  • the formulation below is an example of a built particulate laundry detergent composition that may be used in accordance with the invention.

Abstract

The invention relates to the use of polyvinyl pyrrolidone (PVP) in a laundry detergent composition to improve the oily soil detergency of the composition. The PVP is suitably used in amounts of from 0.5 to 3 wt%, preferably from 1 to 2 wt%. Preferably the detergent composition contains a sulphonate anionic detergent such as linear alkylbenzene sulphonate.

Description

DETERGENT COMPOSITIONS
TECHNICAL FIELD
The present invention relates to laundry detergent compositions containing polyvinyl pyrrolidone. The compositions exhibit improved detergency on oily soils.
BACKGROUND AND PRIOR ART
Polyvinyl pyrrolidone and some related polymers are known ingredients of laundry detergent compositions, providing the benefit of reduced dye transfer between fabrics in a mixed load.
Laundry detergent compositions containing polyvinyl pyrrolidone as a dye transfer inhibitor are disclosed, for example, in WO 92 18597A, WO 94 03567A, WO 95 03390A, WO 95 17496A, WO 95 27028A and WO 95 34627A (Procter 5-
Gamble) , and WO 94 06354A, WO 94 24249A and WO 97 03166A (Henkel) .
GB 1 354 498 (Unilever) discloses laundry detergent compositions containing vinyl pyrrolidone/vinyl acetate copolymers as antiredeposition agents. Polyvinyl pyrrolidone itself is stated to be ineffective. It has now been discovered that polyvinyl pyrrolidone is also effective to enhance oily soil detergency, especially in detergent compositions containing anionic surfactants, more especially alk lbenzene sulphonate.
DEFINITION OF THE INVENTION
The present invention provides the use of polyvinyl pyrrolidone in a laundry detergent composition comprising an organic surfactant and optionally a detergency builder to improve the oily soil detergency of the composition.
The polyvinyl pyrrolidone
The polyvinyl pyrrolidone (hereinafter PVP) preferably has a molecular weight within the range of from 10 000 to 100 000, more preferably from 25 000 to 75 000.
PVP is commercially available, for example, from BASF as the Luviskol (Trade Mark) K series (powders and solutions of various concentrations) and Sokalan (Trade Mark) HP50 (powder) , and from International Specialty Products (ISP) as the ISP-K series.
The laundry detergent composition
In a laundry detergent composition in accordance with the invention, the PVP is present in an amount sufficient to enhance oily soil detergency. Suitably the PVP is present in an amount of from from 0.5 to 3 wt%, preferably from 1 to The detergent composition may suitably comprise:
(a) from 5 to 60 wt%, preferably from 10 to 40 wt%, of organic surfactant,
(b) optionally from 5 to 80 wt%, preferably from 10 to 60 wt%, of detergency builder,
(c) from 0.5 to 3 wt%, preferably from 1 to 2 wt%, of PVP,
(d) optionally other detergent ingredients to 100 wt%.
The organic surfactant
The detergent composition in accordance with the invention may contain any organic surfactants (detergent-active compounds) suitable for incorporation into laundry detergent compositions .
Detergent-active compounds (surfactants) may be chosen from soap and non-soap anionic, cationic, nonionic, amphoteric and zwitterionic detergent-active compounds, and mixtures thereof. Many suitable detergent-active compounds are available and are fully described in the literature, for example, in "Surface-Active Agents and Detergents", Volumes I and II, by Schwartz, Perry and Berch. The preferred detergent-active compounds that can be used are soaps and synthetic non-soap anionic and nonionic compounds. The total amount of surfactant present is suitably within the range of from 5 to 60 wt%, preferably from 5 to 40 wt%. Anionic surfactants are well-known to those skilled in the art. Examples include alkylbenzene sulphonates, particularly linear alkylbenzene sulphonates having an alkyl chain length of Cs-Cis; primary and secondary alkylsulphates, particularly C8-C20 primary alkyl sulphates; alkyl ether sulphates; olefin sulphonates; alkyl xylene sulphonates; dialkyl sulphosuccinates; and fatty acid ester sulphonates. Sodium salts are generally preferred.
Nonionic surfactants that may be used include the primary and secondary alcohol ethoxylates, especially the Ce-C2o aliphatic alcohols ethoxylated with an average of from 1 to 20 moles of ethylene oxide per mole of alcohol, and more especially the C 0-C 5 primary and secondary aliphatic alcohols ethoxylated with an average of from 1 to 10 moles of ethylene oxide per mole of alcohol. Non-ethoxylated nonionic surfactants include alkylpolyglycosides, glycerol monoethers, and polyhydroxyamides (glucamide) .
Cationic surfactants that may be used include quaternary
+ - ammonium salts of the general formula R1R2R3R4N X wherein the R groups are long or short hydrocarbyl chains, typically alkyl, hydroxyalkyl or ethoxylated alkyl groups, and X is a solubilising anion (for example, compounds in which Ri is a c 8-c 22 alkyl group, preferably a Cs-Cio or C12-C14 alkyl group, R2 is a methyl group, and R3 and R4, which may be the same or different, are methyl or hydroxyethyl groups) ; and cationic esters (for example, choline esters) .
Amphoteric surfactants and/or zwitterionic surfactants may also be present.
Preferred amphoteric surfactants are amine oxides. These are materials of the general formula RlR2R3N→0
wherein R is typically a Cs-Cis alkyl group, for example, Ci2~ i alkyl, and R2 and R3 , which may be the same or different, are C1-C3 alkyl or hydroxyalkyl groups, for example, methyl groups. The most preferred amine oxide is coco dimethylamine oxide.
Preferred zwitterionic surfactants are betaines, and especially amidobetaines . Preferred betaines are C8-C 3 alkyl amidoalkylbetaines, for example, coco amidopropyl betaine (CAPB) .
According to a preferred embodiment of the invention, the composition comprises a sulphonate anionic surfactant. According to an especially preferred embodiment, the sulphonate anionic surfactant comprises linear alkylbenzene sulphonate (LAS) .
An especially favourable interaction between LAS and PVP has been observed, giving improved primary detergency on difficult oily soils such as dirty motor oil. Without being bound by theory, it is postulated that the this benefit may be attributed to a reduction in the critical micelle concentration (CMC) of the LAS.
The known benefit of dye transfer inhibition is also observed. Preferably, the compositions contains from 3 to 30 wt%, more preferably from 10 to 25 wt%, of LAS. The optional detergency builder
Preferably, the detergent compositions in accordance with the invention also contain one or more detergency builders . The total amount of detergency builder in the compositions may suitably range from 5 to 80 wt%, preferably from 10 to 60 wt%.
Preferred builders are alkali metal aluminosilicates, more especially crystalline alkali metal aluminosilicates (zeolites) , preferably in sodium salt form.
Zeolite builders may suitably be present in a total amount of from 5 to 60 wt%, preferably from 10 to 50 wt%.
The zeolites may be supplemented by other inorganic builders, for example, amorphous aluminosilicates, or layered silicates such as SKS-6 ex Clariant .
The zeolites may be supplemented by organic builders, for example, polycarboxylate polymers such as polyacrylates and acrylic/maleic copolymers; monomeric polycarboxylates such as citrates, gluconates, oxydisuccinates, glycerol mono-, di- and trisuccinates, carboxymethyloxysuccinates, carboxymethyloxymalonates, dipicolinates, hydroxyethyliminodiacetates, alkyl- and alkenylmalonates and succinates; and sulphonated fatty acid salts. Alternatively, the compositions in accordance with the invention may contain phosphate builders, for example, sodium tripolyphosphate .
Especially preferred organic builders are citrates, suitably used in amounts of from 1 to 30 wt%, preferably from 2 to 15 wt%; and acrylic polymers, more especially acrylic/maleic copolymers, suitably used in amounts of from 0.5 to 15 wt%, preferably from 1 to 10 wt%. Builders, both inorganic and organic, are preferably present in alkali metal salt, especially sodium salt, form.
According to a preferred embodiment of the invention, the detergency builder, which is present in an amount of from 5 to 80 wt%, preferably from 10 to 60 wt%, is selected from sodium tripolyphosphate, zeolites, sodium carbonate and mixtures thereof .
Other detergent ingredients
Detergent compositions in accordance with the invention may also suitably contain a bleach system. Preferably this will include a peroxy bleach compound, for example, an inorganic persalt or an organic peroxyacid, capable of yielding hydrogen peroxide in aqueous solution.
Preferred inorganic persalts are sodium perborate monohydrate and tetrahydrate, and sodium percarbonate, the latter being especially preferred. The sodium percarbonate may have a protective coating against destabilisation by moisture. The peroxy bleach compound is suitably present in an amount of from 5 to 35 wt%, preferably from 10 to 25 wt%. The peroxy bleach compound may be used in conjunction with a bleach activator (bleach precursor) to improve bleaching action at low wash temperatures. The bleach precursor is suitably present in an amount of from 1 to 8 wt%, preferably from 2 to 5 wt%. Preferred bleach precursors are peroxycarboxylic acid precursors, more especially peracetic acid precursors and peroxybenzoic acid precursors; and peroxycarbonic acid precursors. An especially preferred bleach precursor suitable for use in the present invention is N,N,N' ,N' -tetracetyl ethylenediamine (TAED) .
A bleach stabiliser (heavy metal sequestrant) may also be present. Suitable bleach stabilisers include ethylenediamine tetraacetate (EDTA) , diethylenetriamine pentaacetate (DTPA) , ethylenediamine disuccinate (EDDS) , and the polyphosphonates such as the Dequests (Trade Mark) , ethylenediamine tetramethylene phosphonate (EDTMP) and diethylenetriamine pentamethylene phosphate (DETPMP) .
The compositions in accordance with the invention may contain alkali metal, preferably sodium, carbonate, in order to increase detergency and ease processing. Sodium carbonate may suitably be present in amounts ranging from 1 to 60 wt%, preferably from 2 to 40 wt%. As previously indicated, sodium silicate may also be present. The amount of sodium silicate may suitably range from 0.1 to 5 wt%. Sodium silicate, as previously indicated, is preferably introduced via the second base granule . Powder flow may be improved by the incorporation of a small amount of a powder structurant . Examples of powder structurants, some of which may play other roles in the formulation as previously indicated, include, for example, fatty acids (or fatty acid soaps) , sugars, acrylate or acrylate/maleate polymers, sodium silicate, and dicarboxylic acids (for example, Sokalan (Trade Mark) DCS ex BASF) . One preferred powder structurant is fatty acid soap, suitably present in an amount of from 1 to 5 wt%.
Other materials that may be present in detergent compositions in accordance with the invention include antiredeposition agents such as cellulosic polymers; soil release agents; anti-dye-transfer agents; fluorescers; inorganic salts such as sodium sulphate; enzymes
(proteases, Upases, amylases, cellulases) ; dyes; coloured speckles; perfumes; and fabric conditioning compounds. This list is not intended to be exhaustive.
Product form and preparation
The compositions in accordance with the invention may be of any suitable physical form, for example, particulates (powders, granules, tablets), liquids, pastes, gels or bars. According to one especially preferred embodiment of the invention, the detergent composition is in particulate form.
Powders of low to moderate bulk density may be prepared by spray-drying a slurry, and optionally postdosing (dry- mixing) further ingredients. "Concentrated" or "compact" powders may be prepared by mixing and granulating processes, for example, using a high-speed mixer/granulator, or other non-tower processes.
Tablets may be prepared by compacting powders, especially "concentrated" powders.
Also preferred are liquid detergent compositions, which may be prepared by admixing the essential and optional ingredients in any desired order to provide compositions containing the ingredients in the requisite concentrations.
Incorporation of the PVP
The PVP may be incorporated at any suitable stage in the manufacture of the compositions in accordance with the invention. As previously indicated, PVP is commercially available both in solution form and in solid form. For example, in the manufacture of spray-dried particulate compositions, PVP in powder or solution (preferably aqueous) form may be incorporated in the slurry. For non-tower particulates, PVP powder or solution may be easily introduced into mixing and granulating apparatus, either alone or in admixture with other solid or liquid ingredients as appropriate .
EXAMPLES
The invention is further illustrated by the following Examples, in which parts and percentages are by weight unless otherwise stated. EXAMPLES 1 to 8, COMPARATIVE EXAMPLES A and B Detergency benefits on dirty motor oil using model wash liquors
Wash liquors containing 1 g/litre or 2.5 g/litre of a notional detergent composition (the "product") containing linear alkylbenzene sulphonate (LAS) and sodium carbonate were prepared to the following general formulation:
Figure imgf000012_0001
The PVP samples used were as follows
Figure imgf000012_0002
Detergency on white cotton cloth soiled with dirty motor oil was assessed using a high throughput small scale wash method . The wash was carried out in water of 20 (French) hardness (Ca:Mg 2:1), at a temperature of 20 C for 20 minutes .
Whiteness before and after the wash was determined using the technique of colour change by image analysis using a greyness scale. The results are analogous to reflectance changes at 460 nm as measured by a reflectance spectrophotometer and are expressed as ΔR and ΔΔR.
Results at 1 g/litre "product" concentration
Figure imgf000014_0001
Results at 2.5 g/litre "product" concentration
Figure imgf000014_0002
EXAMPLE 9
Particulate detergent composition
The formulation below is an example of a built particulate laundry detergent composition that may be used in accordance with the invention.
Figure imgf000015_0001

Claims

1 Use of polyvinyl pyrrolidone in a laundry detergent composition comprising an organic surfactant and optionally a detergency builder to improve the oily soil detergency of the composition.
2 Use as claimed in any preceding claim, characterised in that the polyvinyl pyrrolidone has a molecular weight within the range of from 10 000 to 100 000, preferably from 25 000 to 75 000.
3 Use as claimed in any preceding claim, characterised in that the laundry detergent composition contains from 0.5 to 3 wt%, preferably from 1 to 2 wt%, of polyvinyl pyrrolidone.
4 Use as claimed in any preceding claim, characterised in that the laundry detergent composition comprises:
(a) from 5 to 60 wt%, preferably from 10 to 40 wt%, of organic surfactant,
(b) optionally from 5 to 80 wt%, preferably from 10 to 60 wt%, of detergency builder,
(c) from 0.5 to 3 wt%, preferably from 1 to 2 wt%, of polyvinyl pyrrolidone, (d) optionally other detergent ingredients to 100 wt%.
5 Use as claimed in any preceding claim, characterised in that the organic surfactant comprises a sulphonate anionic surfactant . 6 Use as claimed in claim 5, characterised in that the organic surfactant comprises linear alkylbenzene sulphonate.
7 Use as claimed in claim 6, characterised in that the laundry detergent composition contains from 3 to 30 wt%, preferably from 10 to 25 wt%, of linear alkylbenzene sulphonate .
8 Use as claimed in any preceding claim, characterised in that the laundry detergent composition comprises from 5 to
80 wt%, preferably from 10 to 60 wt%, of detergency builder selected from sodium tripolyphosphate, zeolites, sodium carbonate and mixtures thereof.
PCT/EP2003/007754 2002-08-10 2003-07-16 Detergent compositions WO2004018603A1 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
DE60305927T DE60305927T2 (en) 2002-08-10 2003-07-16 DETERGENT COMPOSITIONS
BR0312731-1A BR0312731A (en) 2002-08-10 2003-07-16 Use of polyvinyl pyrrolidone
AU2003246709A AU2003246709A1 (en) 2002-08-10 2003-07-16 Detergent compositions
EP03792209A EP1527155B2 (en) 2002-08-10 2003-07-16 Detergent compositions

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB0218634.4A GB0218634D0 (en) 2002-08-10 2002-08-10 Detergent compositions
GB0218634.4 2002-08-10

Publications (1)

Publication Number Publication Date
WO2004018603A1 true WO2004018603A1 (en) 2004-03-04

Family

ID=9942091

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2003/007754 WO2004018603A1 (en) 2002-08-10 2003-07-16 Detergent compositions

Country Status (8)

Country Link
EP (1) EP1527155B2 (en)
AR (1) AR040832A1 (en)
AT (1) ATE328992T1 (en)
AU (1) AU2003246709A1 (en)
BR (1) BR0312731A (en)
DE (1) DE60305927T2 (en)
GB (1) GB0218634D0 (en)
WO (1) WO2004018603A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013034438A1 (en) * 2011-09-09 2013-03-14 Henkel Ag & Co. Kgaa Polymeric agents that improve primary washing efficiency

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102007061861A1 (en) 2007-12-19 2009-06-25 Henkel Ag & Co. Kgaa Detergents or cleaning agents with improved cleaning performance

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3318816A (en) * 1964-11-12 1967-05-09 Colgate Palmolive Co Detergent composition in solid form containing a synergistic mixture of cmc and pvp
EP0262897A2 (en) * 1986-10-01 1988-04-06 Unilever Plc Detergent composition
EP0372291A1 (en) * 1988-11-28 1990-06-13 Henkel Kommanditgesellschaft auf Aktien Laundry process for discoloration-sensitive textiles
WO1995013354A1 (en) * 1993-11-10 1995-05-18 The Procter & Gamble Company Detergent compositions which provide dye transfer inhibition benefits
WO1995023840A1 (en) * 1994-03-04 1995-09-08 The Procter & Gamble Company Polyhydroxy amides to provide dye transfer inhibition benefits during fabric laundering
WO1997023591A1 (en) * 1995-12-21 1997-07-03 Unilever Plc A detergent composition
WO1998054394A1 (en) * 1997-05-28 1998-12-03 Black Robert H Methods of cleaning soiled fabrics
WO1999036493A1 (en) * 1998-01-13 1999-07-22 The Procter & Gamble Company A detergent granule with improved dissolution

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3000830A (en) 1952-12-05 1961-09-19 Fong Willie Use of polyvinylpyrrolidone as a soil-suspending agent
EP0087914B1 (en) 1982-03-01 1986-10-08 The Procter & Gamble Company Detergent composition
SE459972B (en) 1983-03-29 1989-08-28 Colgate Palmolive Co DIRTY REFERENCE PARTICULAR DETERGENT COMPOSITION CONTAINING A DIRT-REFERENCE POLYMER, PROCEDURE FOR ITS PREPARATION AND ITS USE OF WASHING OF SYNTHETIC ORGANIC POLYMER FIBERIAL
EP0781838A1 (en) 1995-12-29 1997-07-02 Colgate-Palmolive Company Detergent composition having improved cleaning power
DE19727476A1 (en) 1997-06-27 1999-01-07 Basf Ag Process for the preparation of low molecular weight homopolymers of N-vinylpyrrolidone
US6130193A (en) 1998-02-06 2000-10-10 Precision Fabrics Group, Inc. Laundry detergent compositions containing silica for laundry detergent sheets
GB0002749D0 (en) 2000-02-07 2000-03-29 Unilever Plc Detergent compositions
EP1167500A1 (en) 2000-06-29 2002-01-02 The Procter & Gamble Company Process of cleaning a hard surface

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3318816A (en) * 1964-11-12 1967-05-09 Colgate Palmolive Co Detergent composition in solid form containing a synergistic mixture of cmc and pvp
EP0262897A2 (en) * 1986-10-01 1988-04-06 Unilever Plc Detergent composition
EP0372291A1 (en) * 1988-11-28 1990-06-13 Henkel Kommanditgesellschaft auf Aktien Laundry process for discoloration-sensitive textiles
WO1995013354A1 (en) * 1993-11-10 1995-05-18 The Procter & Gamble Company Detergent compositions which provide dye transfer inhibition benefits
WO1995023840A1 (en) * 1994-03-04 1995-09-08 The Procter & Gamble Company Polyhydroxy amides to provide dye transfer inhibition benefits during fabric laundering
WO1997023591A1 (en) * 1995-12-21 1997-07-03 Unilever Plc A detergent composition
WO1998054394A1 (en) * 1997-05-28 1998-12-03 Black Robert H Methods of cleaning soiled fabrics
WO1999036493A1 (en) * 1998-01-13 1999-07-22 The Procter & Gamble Company A detergent granule with improved dissolution

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013034438A1 (en) * 2011-09-09 2013-03-14 Henkel Ag & Co. Kgaa Polymeric agents that improve primary washing efficiency

Also Published As

Publication number Publication date
EP1527155A1 (en) 2005-05-04
GB0218634D0 (en) 2002-09-18
ATE328992T1 (en) 2006-06-15
EP1527155B1 (en) 2006-06-07
AU2003246709A1 (en) 2004-03-11
DE60305927D1 (en) 2006-07-20
EP1527155B2 (en) 2011-04-13
DE60305927T2 (en) 2007-06-06
AR040832A1 (en) 2005-04-20
BR0312731A (en) 2005-04-19

Similar Documents

Publication Publication Date Title
EP1558717B1 (en) Laundry detergent composition
EP1305387B1 (en) Coloured speckle composition and particulate laundry detergent compositions containing it
EP1287101B1 (en) Detergent compositions
US6555513B2 (en) Detergent compositions
EP1254202B1 (en) Detergent compositions
EP1539908A1 (en) Detergent compositions
ZA200504393B (en) Laundry detergent compositions containing polymers
EP1527155B1 (en) Detergent compositions
ZA200503245B (en) Laundry detergent composition
EP1299512B1 (en) Detergent compositions
EP1527154B1 (en) Detergent compositions
WO2004027004A1 (en) Detergent compositions
WO2003035822A1 (en) Detergent compositions
ZA200402666B (en) Detergent compositions containing potassium carbonate and process for preparing them.
WO2004027005A1 (en) Detergent compositions

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SY TJ TM TN TR TT TZ UA UG UZ VC VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LU MC NL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
121 Ep: the epo has been informed by wipo that ep was designated in this application
WWE Wipo information: entry into national phase

Ref document number: 2003792209

Country of ref document: EP

WWP Wipo information: published in national office

Ref document number: 2003792209

Country of ref document: EP

WWG Wipo information: grant in national office

Ref document number: 2003792209

Country of ref document: EP

NENP Non-entry into the national phase

Ref country code: JP

WWW Wipo information: withdrawn in national office

Country of ref document: JP