GB2401875A - Aqueous cleaning compositions - Google Patents

Aqueous cleaning compositions Download PDF

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Publication number
GB2401875A
GB2401875A GB0311783A GB0311783A GB2401875A GB 2401875 A GB2401875 A GB 2401875A GB 0311783 A GB0311783 A GB 0311783A GB 0311783 A GB0311783 A GB 0311783A GB 2401875 A GB2401875 A GB 2401875A
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composition
acid
formula
alkyl
che
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GB0311783D0 (en
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Francesca Rosiello
Dora Zamuner
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Reckitt Benckiser NV
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Reckitt Benckiser NV
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Priority to GB0311783A priority Critical patent/GB2401875A/en
Publication of GB0311783D0 publication Critical patent/GB0311783D0/en
Priority to PCT/GB2004/002188 priority patent/WO2004104147A1/en
Publication of GB2401875A publication Critical patent/GB2401875A/en
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    • 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
    • C11D1/34Derivatives of acids of phosphorus
    • C11D1/342Phosphonates; Phosphinates or phosphonites
    • 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
    • C11D1/78Neutral esters of acids of phosphorus

Abstract

A laundry detergent composition comprising: an ethoxylated aliphatic phosphono compound of formula (I) <CHE>(HO)(3-m)OP(R-(CH2-CH2-O)n-R<1>)m</CHE> or <CHE>(HO)(3-m)OP(O-(CH2-CH2-O)n-R<1>)m</CHE> or <CHE>(HO)(3-m)OP(O-R<1>-(CH2-CH2-O)n-H)m</CHE> wherein each n is independently an integer from 1 to 10; each R is independently a 1-14C alkylene or alkenylene chain; and R<1> is 1-14C alkyl or alkenyl chain, provided that the total number of carbons in R and R<1> does not exceed 20, preferably less than 16; at least one additional detersive surfactant; up to 15% by weight of one or more minor ingredients selected from; enzyme, optical brightener, preservative, fragrance and dye; and water.

Description

I
11220P6GB 2401 875 Aqueous Cleaning Compositions The present invention relates to an aqueous liquid fabric detergent that contains a new thickening system, and the use of such compositions in cleaning fabric.
An objective of the present invention is to provide a base composition which is stable and to which ingredients typically found in fabric detergents can be added without any major negative impacts on the comparability of the ingredients. In particular the composition is stable to light, in particular UV light. Preferably the product should also be physically lo stable, as well as chemically stable. Ideally the product is viscose and has a viscosity of greater than 100 cps, preferably greater than 300, 400 or 500 (as measured in a Brookfield viscometer at 20 C, spindle no.2 and 1 S rpm). In addition, preferably, the base composition and the final product is transparent.
We have also found that the cleaning performance of liquid detergent products, either as a stain pre-treater or as a heavy or light duty laundry detergent, is excellent when compared with benchmark commercially available products.
We present as a feature of the invention a (laundry detergent) composition comprising: an ethoxylated aliphatic phosphono compound of formula (I) (HO)(3my0P(R(CH2CH20)nR)m or (HO)(3m)0P(O(CH2CH20)nR)m or (HO)(3m)0P(ORI(CH2-cH2-o)n-H)m wherein each n is independently an integer from I to 10; each R is independently a 1-14C alkylene or alkenylene chain; and Rt is 1-14C alkyl or alkenyl chain, provided that the total number of carbons in R and R' does not exceed 20, preferably less than 16; r 1 1 220P6GB at least one additional detersive surfactant; up to 15% by weight of one or more minor ingredients selected from; enzyme, optical brightener, preservative, fragrance and dye; and water.
We have found that the compound of formula (I) provides the composition with very good aesthetic properties - a transparent gel - and helps stabilise the formula even at high temperatures (around 40 C for up to 6 months).
Preferably the compound of formula (I) is present in an amount of up to 20% wt. ideally up to 15% wt or 10% wt. Preferred minimum amounts are 1% wt. 5% wt or 3% wt.
Preferably a bleaching agent and/or a building agent is added to the composition, as described below.
Examples of preferred additional detersive surfactants considered in this invention are either anionic or non-ionic surfactants and mixtures thereof. Preferred total levels of additional detersive surfactants are from 1 to 50%wt, ideally from 10 to 40%wt and preferably 20 to 35%wt.
Non-ionic Surfactant The non-ionic surfactant is preferably a linear surfactant having a formula RO(CH2CH20)nH wherein R is a saturated or unsaturated (preferably saturated) hydrocarbon chain ranging from C 12 to C 16 and n represents the number of repeating units and is a number of from about 1 to about 12. Examples of other non-ionic surfactants include higher aliphatic primary alcohols containing 12 to 16 carbon atoms which are condensed with about three to thirteen moles of ethylene oxide.
Other examples of non-ionic surfactants include primary alcohol ethoxylates # 1 1220P6GB Other examples of non-ionic surfactants suitable for use in the present invention include ethylene oxide condensate products of secondary aliphatic alcohols containing 11 to 18 carbon atoms in a straight or branched chain configuration condensed with 5 to 30 moles of ethylene oxide. Examples of commercially available non-ionic detergents of the foregoing type are C1 1-15 secondary alkanol condensed with either 9 moles of ethylene oxide (such as Tergitol 15-S-9) or 12 moles of ethylene oxide (such as Tergitol 15-S-12) marketed by Union Carbide, a subsidiary of Dow Chemical.
0 Octylphenoxy polyethoxyethanol type non-ionic surfactants, for example, Triton X-100, as well as amine oxides can also be used as a non-ionic surfactant in the present invention.
A further preferred class of non-ionic surfactants are the C 1 020alkanol amides, the amide being formed from a mono or di C24alkanolamine.
Anionic Surfactant A preferred surfactant is an anionic surfactant. The anionic sulphates are preferably present at a level of at least 8% wt of the composition. More preferably these anionic surfactant is present at a level of from 10% to 40%, more preferably from 15% or even 18% to 30% wt of the composition. Preferred amounts of the alkyl sulphate surfactant, are from 16% to 40%, or more preferably 18% to 25% wt of the detergent composition.
Such anionic surfactants are frequently provided in a salt form, such as alkali metal salts, ammonium salts, amine salts, amino alcohol salts or magnesium salts. Contemplated as useful are one or more sulfate or sulfonate compounds including: alkyl sulfates, alkyl ether sulfates, alkylamidoether sulfates, alkyl benzene sulfates, alkyl benzene sulfonates, alkylaryl polyether sulfates, monoglyceride sulfates, alkylsulfonates, alkylamide sulfonates, alkylarylsulfonates, olefinsulfonates, paraffn sulfonates, alkyl sulfosuccinates, alkyl ether sulfosuccinates, alkylamide sulfosuccinates, alkyl sulfosuccinamate, alkyl sulfoacetates, alkyl carboxylates, alkyl phosphates, alkyl ether phosphates, acyl sarconsinates, acyl isethionates, and N-acyl taurates. Generally, the alkyl 1 1 220P6GB or acyl radical in these various compounds comprise a carbon chain containing 12 to 20 carbon atoms.
Preferred surfactants are also alkyl naphthalene sul fonate anionic surfactants of the formula: R 3 SO3M wherein R is a straight chain or branched alkyl chain having from about I to about 25 carbon atoms, saturated or unsaturated, and the longest linear portion of the alkyl chain is carbon atoms or less on the average, M is a cation which makes the compound water soluble especially an alkali metal such as sodium or magnesium, ammonium or Particularly preferred are alkyl sulfate anionic surfactants of the formula (II) (II) R-O (CH2Cll2o)x S O-M wherein R is a straight chain or branched alkyl chain having from about 8 to about 18 carbon atoms, saturated or unsaturated, and the longest linear portion of the alkyl chain is no more thanl 5 carbon atoms, M is a cation, preferably one which makes the compound water-soluble especially an alkali metal such as sodium or magnesium, ammonium or substituted ammonium cation, and x is from 0 to about 4, preferably x is 2 or 3, ideally x is 2. When x is 0 then most preferred are the non-ethoxylated C12-15 primary and secondary alkyl sulfates, especially sodium lauryl sulfate.
It is preferred that the anionic surfactants herein are present in the form of sodium salts.
1 1220P6GB In a preferred feature of the invention we have found that transparent viscose compositions of the invention are ideally formed from the combination of compounds of formula (l), (II) and a C10-20alkanol amide, the amide is preferably a C10-20 alkanolamide of a mono or di C2-4 alkanolamine, ideally in an amount of up to 20% wt.
ideally up to 15% wt or 10% wt. Suitable minimum amounts are from 1% wt. 2% wt or 3%wt.
We present as a further feature of the invention an aqueous liquid laundry detergent composition comprising a compound of formula (I); a compound of formula (II); a C10-20alkanol amide, the amide is preferably a C10-20 alkanolamide of a mono or di C2-4alkanolamine; and water.
The compound of formula (ll) is present in the composition in an amount of up to 20% wt. ideally up to 18% wt or 10% wt. Suitable minimum amounts are from 1% wt. 2% wt or3% We present as a further feature of the invention a method of cleaning fabric which method comprises applying a composition as described herein to the fabric.
Bleaching Agent An optional ingredient is bleaching agent which comprises a source of active oxygen and, optionally, a bleach activator. Preferred levels of bleaching agent, including bleach activator, if present, are up to 50%, 40%, 30% or 20% wt. A preferred source of active oxygen according to the present invention is hydrogen peroxide or sources thereof. As used herein a hydrogen peroxide source refers to any water-soluble sources of hydrogen peroxide. Suitable water-soluble sources of hydrogen peroxide for use herein include percarbonates, organic or inorganic peroxides and perforates.
1 1220P6GB Hydrogen peroxide or sources thereof provide from 0. 1% to 15%, preferably from 0.5% to 10%, most preferably from 1% to 5% wt of the total composition of active oxygen.
As used herein active oxygen concentration refers to the percentage concentration of elemental oxygen, with an oxidation number zero, that being reduced to water would be stoichiometrically equivalent to a given percentage concentration of a given peroxide compound, when the peroxide functionality of the peroxide compound is completely reduced to oxides. The active oxygen sources according to the present invention increase lo the ability of the compositions to remove oxidisable stains, to destroy malodourous molecules and to kill germs.
The concentration of available oxygen can be determined by methods known in the art, such as the iodimetric method, the permanganometric method and the cerimetric method.
Said methods and the criteria for the choice of the appropriate method are described for example in "Hydrogen Peroxide", W. C. Schumo, C. N. Satterfield and R. L. Wentworth, Reinhold Publishing Corporation, New York, 1955 and "Organic Peroxides", Daniel Swern, Editor Wiley Int. Science, 1970.
Suitable organic and inorganic peroxides for use in the compositions according to the present invention include diacyl and dialkyl peroxides such as dibenzoyl peroxide, dilauroyl peroxide, dicumyl peroxide, persulphuric acid and mixtures thereof.
Suitable preformed peroxyacids for use in the compositions according to the present invention include diperoxydodecandioic acid DPDA, magnesium perphthalatic acid, pcrlauric acid, perbenzoic acid, diperoxyazelaic acid and mixtures thereof. The compositions according to the present invention comprise from 0% to 15%, preferably from 0.005% to 10% wt of the total composition of said preformed peroxyacids.
Suitable water-soluble builder compounds include the water soluble monomeric carboxylates, or their acid forms, or polycarboxylates or acids thereof home or copolymeric polycarboxylic acids or their salts in which the polycarboxylic acid l 1220P6GB comprises at least two carboxylic radicals separated from each other by not more that two carbon atoms, berates, and mixtures of any of the foregoing.
5] The carboxylate or polycarboxylate builder can be momomeric or oligomeric in type although monomeric polycarboxylates are generally preferred for reasons of cost and performance. The parent acids of the monomeric or oligomeric polycarboxylate chelating agents or mixtures thereof with their salts, e.g. citric acid or citrate/citric acid mixtures are also contemplated as useful builder components.
The monomeric carboxylic acids and salts thereof include the highly preferred fatty acid lo or salts, as described above.
7] Also highly preferred are citric acid and/or sodium citrate builders, preferably present at a level of 1% to 20%, more preferably from 3% to 15%, more preferably from 5% to 12% by weight of the composition.
Borate or boric acid builders, as well as builders containing borateforming materials that can produce borate under detergent storage or wash conditions are useful water-soluble builders herein.
The detergent compositions of the invention may comprise phosphatecontaining builder material. Preferably present at a level of from 2% to 40%, more preferably from 3% to 30%, more preferably from 5% to 20%. Suitable examples of water-soluble phosphate builders are the alkali metal tripolyphosphates, sodium, potassium and ammonium pyrophosphate, sodium and potassium and ammonium pyrophosphate, sodium and potassium orthophosphate, sodium polymeta/phosphate in which the degree of polymerization ranges from about 6 to 21, and salts of physic acid.
The compositions in accord with the present invention may contain a partially soluble or insoluble builder compound, typically present in detergent compositions at a level of from 0.5% to 60% by weight, preferably from 5% to 50% by weight, most preferably from 8% to 40% weight of the composition.
Preferred are aluminosilicates and/or crystalline layered silicates such as SKS-6, available 1 1 220P6GB from Clariant.
The compositions of the invention preferably contain as an optional component a heavy metal ion sequestrant. By heavy metal ion sequestrant it is meant herein components which act to sequester (chelate) heavy metal ions. These components may also have calcium and magnesium chelation capacity, but preferentially they show selectivity to binding heavy metal ions such as iron, manganese and copper.
Heavy metal ion sequestrants are generally present at a level of from 0. 005% to 10%, 0 preferably from 0.1% to 5%, more preferably from 0.25% to 7.5% and most preferably from 0.3% to 2% by weight of the compositions.
Suitable heavy metal ion sequestrants for use herein include organic phosphonates, such as the amino alkylene poly (alkylene phosphonates), alkali metal ethane l-hydroxy disphosphonates and nitrite trimethylene phosphonates.
Preferred among the above species are diethylene triamine penta (methylene phosphonate), ethylene diamine tri (methylene phosphonate) hexamethylene diamine tetra (methylene phosphonate) and hydroxy-ethylene 1,1 diphosphonate, 1, I hydroxyethane diphosphonic acid and 1,1 hydroxyethane dimethylene phosphoric acid.
Other suitable heavy metal ion sequestrant for use herein include nitrilotriacetic acid and polyaminocarboxylic acids such as ethylenediaminotetracetic acid, ethylenediamine disuccinic acid, ethylenediamine diglutaric acid, 2-hydroxypropylenediamine disuccinic acid or any salts thereof.
Other suitable heavy metal ion sequestrants for use herein are iminodiacetic acid derivatives such as 2-hydroxyethyl diacetic acid or glyceryl imino diacetic acid, described in EP-A-317,542 and EP-A-399,133. The iminodiacetic acid-N-2 hydroxypropyl sulfonic acid and aspartic acid N-carboxymethyl N-2-hydroxypropyl-3 sulfonic acid sequestrants described in EP-A-516,102 are also suitable herein. The beta ] 1 220P6GB alanine-N,N'-diacetic acid, aspartic acid-N,N'-diacetic acid, aspartic acid-N-monoacetic acid and iminodisuccinic acid sequestrants described in EP-A-509,382 are also suitable.
EP-A-476,257 describes suitable amino based sequestrants. EP-A-510,331 describes suitable sequestrants derived from collagen, keratin or casein. EP-A-528,859 describes a suitable alkyl iminodiacetic acid sequestrant. Dipicolinic acid and 2-phosphonobutane 1,2,4-tricarboxylic acid are alos suitable. Glycinamide-N,N'-disuccinic acid (GADS), ethylenediamine-N-N'-diglutaric acid (EDDG) and 2hydroxypropylenediamine-N-N' disuccinic acid (HPDDS) are also suitable.
Especially preferred are diethylenetriarnine pentacetic acid, ethylenediamine-N,N' disuccinic acid (EDDS) and 1,1 hydroxyethane diphosphonic acid or the alkali metal, alkaline earth metal, ammonium, or substituted ammonium salts thereof, or mixtures thereof.
Enzyme The composition herein preferably comprises an enzyme or enzymes. Preferred additional enzymatic materials include the commercially available lipases, cutinases, amylases, neutral and alkaline proteases, esterases, cellulases, pectinases, lactases and peroxidases conventionally incorporated into detergent compositions. Suitable enzymes are discussed in US3,519,570 and 3,533,139.
Preferred commercially available protease enzymes include those sold under the tradenames Alcalase, Savinase, Primase, Durazym, and Esperase by Novo Industries A/S (Denmark), those sold under the tradename Maxatase, Maxacal and Maxapem by Gist Brocades, those sold by Genencor International, and those sold under the tradename Opticlean and Optimase by Solvay Enzymes. Protease enzyme may be incorporated into the compositions in accordance with the invention at a level of from 0.0001 % to 4% active enzyme by weight of the composition.
1 1220P6GB Preferred amylases include, for example, [alpha]-amylases obtained from a special strain of B licheniforrnis, described in more detail in GB-1,269,839 (Novo). Preferred commercially available amylases include for example, those sold under the tradename Rapidase by GistBrocades, and those sold under the tradename Termamyl and BAN by s Novo Industries A/S. Amylase enzyme may be incorporated into the composition in accordance with the invention at a level of from 0.0001 % to 2% active enzyme by weight of the composition.
Lipolytic enzyme may be present at levels of active lipolytic enzyme of from 0.0001% to 0 10% by weight of the particle, preferably 0.001 % to 3% by weight of the composition, most preferably from 0.001 % to 0.5% by weight of the compositions. The lipase may be fungal or bacterial in origin being obtained, for example, from a lipase producing strain of Humicola sp., Thermomyces sp. or Pseudomonas sp. including Pseudomonas pseudoalcaligenes or Pseudomas fluorescent. Lipase from chemically or genetically modified mutants of these strains are also useful herein. A preferred lipase is derived from Pseudomonas pseudoalcaligenes, which is described in Granted European Patent, EP-B-0218272. Another preferred lipase herein is obtained by cloning the gene from Humicola lanuginosa and expressing the gene in Aspergillus oryza, as host, as described in European Patent Application, EP-A-0258 068, which is commercially available from Novo Industri A/S, Bagsvaerd, Denmark, under the trade name Lipolase. This lipase is also described in U.S. Pat. No. 4,810,414, Huge-Jensen et al, issued Mar. 7, 1989.
Optical Brightener The compositions herein also optionally contain from about 0.005% to 5% by weight of certain types of hydrophilic optical brighteners.
Preferred brighteners include 4,4',-bis[(4-anilino-6-(N-2-bishydroxyethyl)-s-triazine-2 yl)amino]-2,2'-stilbenedisulfonic acid and disodium salt, commercially marketed under the tradename Tinopal-UNPA-GX by Ciba-Geigy Corporation; 4,4'-bis[(4-anilino-6-(N 2-hydroxyethyl-N-methylamino)-s-triazine-2-yl)amino]2,2'stilbenedisulfonic acid disodium salt, commercially marketed under the tradename Tinopal 5BM-GX by Ciba e ' 1 1 220P6GB Geigy Corporation; 4,4'-bis[(4-anilino-6-morphilino-s- triazine-2-yl)amino]2,2' stilbenedisulfonic acid, sodium salt, commercially marketed under the tradename Tinopal-DMS-X and Tinopal AMS- GX by Ciba Geigy Corporation.
Fragrance Preferably, the composition herein comprises (by weight) from 0. 01% to 10%, preferably from 0.1% to 2% perfume. The perfume for use herein may be a spray-on perfume, an encapsulated perfume or a combination thereof. A typical perfume for use herein is 0 described in U.S. patent application Ser. No. I]S99/15666.
Builder Agent The compositions in accord with the present invention preferably contain a builder agent, typically present in detergent compositions at a level of from 1% to 60% wt. preferably i from 3% to 40% wt. most preferably from 5% to 25% wt of the composition.
The compositions according to the present invention may further comprise a builder system. Any conventional builder system is suitable for use herein including; aluminosilicate materials, silicates, polycarboxylates, alkyl-or alkenylsuccinic acid and fatty acids, materials such as ethylenediamine tetraacetate, diethylene triamine pentamethyleneacetate, metal ion sequestrants such as aminopolyphosphonates, particularly ethylenediamine tetramethylene phosphoric acid and diethylene triamine pentamethylenephosphonic acid. However, water-soluble builders are preferred, such as polycarboxylates, alley-or alkenylsuccinic acid and fatty acids.
Phosphate builders can also be used herein.
Suitable builders can be an inorganic ion exchange material, commonly an inorganic hydrated aluminosilicate material, more particularly a hydrated synthetic zeolite such as I hydrated zeolite A, X, B. HS or MAP. t
1 1 220P6GB Another suitable inorganic builder material is layered silicate, e. g. SKS-6 (Hoechst).
SKS-6 is a crystalline layered silicate consisting of sodium silicate (Na2Si2O5).
Suitable Polycarboxylates containing one carboxy group include lactic acid, glycolic acid s and ether derivatives thereof as disclosed in BE831, 368,821,369 and 821,370.
Polycarboxylates containing two carboxy groups include the water-soluble salts of succinic acid, malonic acid, (ethylenedioxy) diacetic acid, maleic acid, diglycollic acid, tartaric acid, tartronic acid and fumaric acid, as well as the ether carboxylates described in German Offenlegenschrift 2,446,686, and 2,446,687 and U. S. Patent No. 3,935,257 0 and the sulfinyl carboxylates described in Belgian Patent No. 840,623. Polycarboxylates containing three carboxy groups include, in particular, water-soluble citrates, aconitrates and citraconates as well as succinate derivatives such as the carboxymethyloxysuccinates described in British Patent No. 1,379,241, lactoxysuccinates described in Netherlands Application 7205873, and the oxypolycarboxylate materials such as 2-oxa-1, 1,3-propane tricarboxylates described in British Patent No. 1,387,447.
Polycarboxylates containing four carboxy groups include oxydisuccinates disclosed in GB 1,261,829, 1,1,2,2-ethane tetracarboxylates, 1,1,3,3-propane tetracarboxylates and 1,1,2,3-propane tetracarboxylates.
Polycarboxylates containing sulfo substituents include the sulfosuccinate derivatives disclosed in GB1,398,421 and 1,398,422 and in US3,936,448, and the sulfonate pyrolyse citrates described in GBI,082,179, while polycarboxylates containing phosphone substituents are disclosed in GB1, 439,000.
Alicyclic and heterocyclic polycarboxylates include cyclopentane-cis, cis, cis tetracarboxylates, cyclopentadienide pentacarboxylates, 2, 3,4,5tetrabydro-furan -cis, cis, cis-tetracarboxylates, 2,5-tetrahydro-furan-cis-dicarboxylates, 2,2,5,5 tetrahydrofurantetracarboxylates, 1,2,3,4,5,6-hexane-hexacar-boxylates and and carboxymethyl derivatives of polyhydric alcohols such as sorbitol, mannitol and xylitol. Aromatic poly carboxylates include mellitic acid, pyromellitic acid and the phthalic acid derivatives disclosed in GB1,425, 343.
1 1220P6GB Of the above, the preferred polycarboxylates are hydroxycarboxylates containing up to three carboxy groups per molecule, more particularly citrates.
Other builder materials that can form part of the builder system for use in granular compositions include inorganic materials such as alkali metal carbonates, bicarbonates, silicates, and organic materials such as the organic phosphonates, amino polyalkylene phosphonates and amino polycarboxylates.
Other suitable water-soluble organic salts are the homo-or co-polymeric acids or their 0 salts, in which the polycarboxylic acid comprises at least two carboxyl radicals separated from each other by not more than two carbon atoms.
Polymers ofthis type are disclosed in GBI,596,756. Examples of such salts are polyacrylates of MW 2000-5000 and their copolymers with maleic anhydride, such copolymers having a molecular weight of from 20,000 to 70, 000, especially about 40,000.
Also preferred may be, minor ingredients, neutralizing agents, buffering agents, phase regulants, hydrotropes, enzyme stabilizing agents, opacifiers, anti-oxidants, bactericides, photo-bleaches.
Suitably the composition is an aqueous composition, preferably comprising water in an amount of at least 50%wt, more preferably at least 60%wt of the total weight of the composition.
Suitable inorganic salts include metal oxides and halides, such as calcium chloride, for
example.
Suitable buffers include borate buffers, for example.
Preferably the composition in the form of a stain pretreating composition which is applied onto a fabric item prior to it being washed. The composition is packaged in suitable 1 1220P6GB packaging to facilitate application of the composition to the fabric. The packaging could comprise, a squeezy bottle, a roller ball applicator or a spray device. An item of packaging containing the composition may constitute a further aspect of the invention, especially where the packaging item is transparent, given the light stability of the product.
Preferably the packaging item is transparent. A feature of the invention is that transparent packaging items do not need to have included a UV filter.
A further feature of the invention is a method of treating stains on fabric which method comprises applying a composition as described herein to the stained fabric.
The invention is illustrated by the following examples I Raw Materials wt % Oxo Alcohol C1 3-C15 + 7EO Oxo Alcohol C13-C15 + 3 3EO Sodium Lauryl sulphate 1 (2EO)
-
Monafax phosphono 6 surfactant ___ Coconut diethanolamide Fragrance/Dye 0. 2 Sodium hydroxide (10%) 3.54 Preservative 0.02 Deionized Water to 100% 2 - Raw Materials wt % __ _. _ ___ Oxo Alcohol C 1 3-C 15 + 10 7EO 1 1220P6Gs oriloo'Cl] Eli+ 1 3EO Sodium Lauryl sulphate 8 (2EO) = Monafax phosphono 8 surfactant l Coconut dethanolamide Fragrance/Dye 0.2 Sodium hydroxide (10%) Preservative 0.02 Deomzed Water to 100% 3 - Raw Materials -wt /0- Oxo Alcohol C 1 3-C 15 + 6 7EO Oxo Alcohol C 1 3-C 15 + 1 3EO I: Sodium Lauryl sulphate 3 (2EO) Monafax phosphono 4 surfactant Coconut diethanolamide 3.5 Fragrance/Dye 0.4 Sodium hydroxide (10%) 3.5 Preservative 0.02 Deionized Water to 100%

Claims (6)

1 1220P6GB Claims 1. A composition comprising: an ethoxylated aliphatic
phosphono compound of formula (I) (HO)(3m)0P(R(CH2-Cli2-O)n-R)m or (HO)(3m)0P(O(CH2CH20)nRI)m lo or (HO)(3-m)OP(O-RI-(CH2CH2o)n-H)m wherein each n is independently an integer from I to 10; each R is independently a 1-14C alkylene or alkenylene chain; and Ri is 1-14C alkyl or alkenyl chain, provided that the total number of carbons in R and R' does not exceed 20, preferably less than 16; at least one additional detersive surfactant; up to 15% by weight of one or more minor ingredients selected from; enzyme, optical brightener, preservative, fragrance and dye; and water.
2. A composition comprising a compound of formula (I); a compound of formula (Il); a C10-20alkanol amide, the amide is preferably a C10-20 alkanolamide of a mono or di C2-4alkanolamine; and water.
1 1220P6GB
3. A composition as claimed in claim 1 or 2, wherein the composition additionally comprises 0. 1% to 15% by weight of the total composition of active oxygen.
4. A composition as claimed in either any claim from 1 to 3, wherein additional detersivc surfactants are present which comprises a mixture of at least one anionic and at least one nonionic surfactant.
5. A transparent packaging item containing a composition as claimed in any claim o from 1 to4.
6. A method of cleaning fabric which method comprises applying a composition as claimed in any claim from I to 4 to the fabric.
GB0311783A 2003-05-22 2003-05-22 Aqueous cleaning compositions Withdrawn GB2401875A (en)

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Cited By (1)

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US7658953B2 (en) 2006-01-13 2010-02-09 Aseptix Research B.V. Enhanced activity biocidal hydrogen peroxide composition

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11273625B2 (en) 2018-12-21 2022-03-15 The Clorox Company Process for manufacturing multi-layer substrates comprising sandwich layers and polyethylene
EP3945977A4 (en) 2019-04-02 2022-10-12 The Clorox Company Process for manufacturing multi-layer substrates comprising sandwich layers and polyethylene

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2635034A1 (en) * 1975-08-06 1977-02-24 Gaf Corp Aerosol compsns. for pre-laundering heavily soiled fabrics - contain a phosphated anionic surfactant
US5294644A (en) * 1986-06-27 1994-03-15 Isp Investments Inc. Surface active lactams
WO2000023553A1 (en) * 1998-10-16 2000-04-27 S.C. Johnson & Son, Inc. Scrub free formulation for cleaning surfaces

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3265625A (en) * 1962-10-30 1966-08-09 C P Baker & Company Liquid detergent
US3704262A (en) * 1970-03-19 1972-11-28 Gaf Corp Surfactant for electrolyte-containing processing solutions
GB1315363A (en) * 1970-05-29 1973-05-02 Unilever Ltd Liquid detergents
DE2211868A1 (en) * 1972-03-11 1973-09-13 Pfersee Chem Fab Simultaneous washing, degreasing desizing and - bleaching of (non) woven fabrics - contg novel p-contg emulsifiers
GB1423166A (en) * 1972-04-11 1976-01-28 Unilever Ltd Detergent composition
US3956198A (en) * 1972-12-15 1976-05-11 Days-Ease Home Products Corporation Liquid laundry washing-aid
US4321256A (en) * 1979-07-19 1982-03-23 Lever Brothers Company Shampoo containing a polyglycol-polyamine condensation resin and a phosphate ester
GB2058823B (en) * 1979-09-17 1983-06-22 Unilever Ltd Dishwashing compositions
US4891148A (en) * 1985-08-05 1990-01-02 Colgate-Palmolive Company Low phosphate or phosphate free nonaqueous liquid nonionic laundry detergent comopsition and method of use
GB8830296D0 (en) * 1988-12-28 1989-02-22 Unilever Plc Bleaching composition
DE4418847A1 (en) * 1994-05-30 1995-12-07 Henkel Kgaa Bleaching and cleaning compsn.
DE19623571C2 (en) * 1996-06-13 2000-06-08 Cognis Deutschland Gmbh Thickener for aqueous hydrogen peroxide solutions
JP3908420B2 (en) * 1999-10-12 2007-04-25 花王株式会社 Cleaning composition
US6566313B1 (en) * 2000-09-15 2003-05-20 Henkel Corporation Shampoo and body wash composition and method of use thereof

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2635034A1 (en) * 1975-08-06 1977-02-24 Gaf Corp Aerosol compsns. for pre-laundering heavily soiled fabrics - contain a phosphated anionic surfactant
US5294644A (en) * 1986-06-27 1994-03-15 Isp Investments Inc. Surface active lactams
WO2000023553A1 (en) * 1998-10-16 2000-04-27 S.C. Johnson & Son, Inc. Scrub free formulation for cleaning surfaces

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7658953B2 (en) 2006-01-13 2010-02-09 Aseptix Research B.V. Enhanced activity biocidal hydrogen peroxide composition

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