WO2004067194A2 - Aqueous cleaning compositions - Google Patents

Aqueous cleaning compositions Download PDF

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Publication number
WO2004067194A2
WO2004067194A2 PCT/GB2004/000393 GB2004000393W WO2004067194A2 WO 2004067194 A2 WO2004067194 A2 WO 2004067194A2 GB 2004000393 W GB2004000393 W GB 2004000393W WO 2004067194 A2 WO2004067194 A2 WO 2004067194A2
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Prior art keywords
composition
formula
compound
hydrogen peroxide
chain
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PCT/GB2004/000393
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French (fr)
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WO2004067194A3 (en
Inventor
Stefano Arrigoni
Francesca Rosiello
Dora Zamuner
Original Assignee
Reckitt Benckiser N.V.
Reckitt Benckiser (Uk) Limited
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Application filed by Reckitt Benckiser N.V., Reckitt Benckiser (Uk) Limited filed Critical Reckitt Benckiser N.V.
Priority to AU2004208552A priority Critical patent/AU2004208552B2/en
Priority to DE602004002462T priority patent/DE602004002462T2/en
Priority to EP04706720A priority patent/EP1597342B1/en
Publication of WO2004067194A2 publication Critical patent/WO2004067194A2/en
Publication of WO2004067194A3 publication Critical patent/WO2004067194A3/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
    • C11D3/39Organic or inorganic per-compounds
    • C11D3/3942Inorganic per-compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/65Mixtures of anionic with cationic compounds
    • C11D1/652Mixtures of anionic compounds with carboxylic amides or alkylol amides
    • 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
    • C11D3/36Organic compounds containing phosphorus
    • C11D3/361Phosphonates, 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
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/39Organic or inorganic per-compounds
    • C11D3/3947Liquid 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
    • 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
    • C11D1/29Sulfates of polyoxyalkylene ethers
    • 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
    • C11D1/38Cationic compounds
    • C11D1/52Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
    • C11D1/523Carboxylic alkylolamides, or dialkylolamides, or hydroxycarboxylic amides (R1-CO-NR2R3), where R1, R2 or R3 contain one hydroxy group per alkyl group

Definitions

  • the present invention relates to stabilised aqueous compositions that contain hydrogen peroxide, an ethoxylated aliphatic phospono surfactant of formula (I), at least one additional detersive surfactant.
  • One drawback to the use of hydrogen peroxide compositions is that without the use of a stabiliser, or a combination of stabilisers, the aqueous peroxide compositions characteristically decompose over a relatively short time period.
  • the actual rate at which hydrogen peroxide compositions decompose will, of course, be dependent upon such factors as pH and the presence of trace amounts of various metal impurities, such as copper or chromium, which may act to catalytically decompose the same.
  • the rate of decomposition of such dilute hydrogen peroxide compositions is greatly accelerated.
  • An objective of the present invention is to provide a hydrogen peroxide containing composition that is stable to light, in particular TJV light.
  • the product should also be physically stable, as well as chemically stable.
  • the product is viscous 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 15 rpm).
  • the product is transparent.
  • 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).
  • Hydrogen peroxide is commercially available in different grades, at 8%, 35% and 50%w/v active, and it is generally stabilised by the use of chelating agents.
  • Preferred levels of hydrogen peroxide are 0.1%w/v to 12%w/v, preferably from 2%w/v to 10%w/v, and ideally from 4%w/v to 9%w/v.
  • Examples of preferred detersive surfactants considered in this invention are either anionic or non-ionic surfactants and mixtures thereof.
  • Preferred total levels of surfactant are from 1 to 50% w/v, ideally from 10 to 40%w/v and preferably 20 to 35%w/v.
  • the non-ionic surfactant is preferably a surfactant having a formula RO(CH2CH2O)nH wherein R is a saturated or unsaturated (preferably saturated) hydrocarbon chain ranging from C12 to C16 and n represents the number of repeating units and is a number of from 1 to 12.
  • R is a saturated or unsaturated (preferably saturated) hydrocarbon chain ranging from C12 to C16 and n represents the number of repeating units and is a number of from 1 to 12.
  • examples of other non-ionic surfactants include higher aliphatic primary alcohols containing 12 to 16 carbon atoms which are condensed with three to thirteen moles of ethylene oxide.
  • non-ionic surfactants include primary alcohol ethoxylates
  • 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 Cll-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.
  • 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 C10-20alkanol amides, the amide being a mono or di C2-4alkanolamine.
  • a preferred surfactant is an anionic surfactant.
  • 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, alkylarnide sulfonates, alkylarylsulfonates, olefinsulfonates, paraffin sulfonates, alkyl sulfosuccinates, alkyl ether sulfosuccinates, alkylarnide sulfos
  • Preferred surfactants are also alkyl naphthalene sulfonate anionic surfactants of the formula: R
  • R is a straight chain or branched alkyl chain having from about 1 to about 25 carbon atoms, saturated or unsaturated, and the longest linear portion of the alkyl chain is 15 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 substituted ammonium cation.
  • alkyl sulfate anionic surfactants of the formula (II)
  • 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 thanl5 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
  • x is from 0 to about 4, preferably x is 2 or 3, ideally x is 2.
  • x is 0 then most preferred are the non-ethoxylated C12-15 primary and secondary alkyl sulfates, especially sodium lauryl sulfate.
  • transparent viscous compositions of the invention are ideally formed from the combination of compounds of formula (I), (II) and C10-20alkanol amides, the amide is preferably a C 10-20 alkanolamide of a mono or di C2-4 alkanolamine.
  • the composition may include one or more further optional ingredients, such as buffers, inorganic salts, fragrance, chelating agents, dispersants, enzyme stabilisers, solvents, dye transfer inhibitors and polymers.
  • the total amount of optional ingredients present in the composition is up to 25%w/v, ideally up to 20%w/v, or up to 15%w/v.
  • Suitable inorganic salts include metal oxides and halides, such as calcium chloride, for example.
  • pH buffers may be added to the composition in an amount of up to 5%w/v
  • suitable buffers include borate buffers.
  • Stabilising Agent Suitable stabilising agents include chelating agents, radical scavengers, antioxidants and mixtures of any thereof.
  • compositions of the present invention may comprise a chelating agent or a mixture thereof as a preferred optional ingredient.
  • Suitable chelating agents may be any of those known to those skilled in the art such as the ones selected from the group comprising phosphonate chelating agents, amino carboxylate chelating agents, other carboxylate chelating agents, polyfunctionally-substituted aromatic chelating agents, ethylenediamine N,N'-disuccinic acids, or mixtures thereof.
  • the chelating agents inactivate the metal ions present on the surface of the fabrics and/or in the cleaning compositions (neat or diluted) that otherwise would contribute to the radical decomposition of any peroxygen bleach.
  • Suitable phosphonate chelating agents to be used herein may include alkali metal ethane 1-hydroxy diphosphonates (HEDP) also known as ethydronic acid, alkylene poly (alkylene phosphonate), as well as amino phosphonate compounds, including amino aminotri(methylene phosphonic acid) (ATMP), nitrilo trimethylene phosphonates (NTP), ethylene diamine terra methylene phosphonates, and diethylene triamine penta methylene phosphonates (DTPMP).
  • the phosphonate compounds may be present either in their acid form or as salts of different cations on some or all of their acid functionalities.
  • Preferred phosphonate chelating agents to be used herein are diethylene triamine penta methylene phosphonate (DTPMP) and ethane 1-hydroxy diphosphonate (HEDP or ethydronic acid). Such phosphonate chelating agents are commercially available from Monsanto under the trade name DEQUEST®.
  • Polyfunctionally-substituted aromatic chelating agents may also be useful in the compositions herein. See U.S. Pat. No. 3,812,044, issued May 21, 1974, to Connor et al.
  • Preferred compounds of this type in acid form are dihydroxydisulfobenzenes such as 1,2- dihydroxy -3,5- disulfobenzene.
  • a preferred biodegradable chelating agent for use herein is ethylene diamine N,N'- disuccinic acid, or alkali metal, or alkaline earth, ammonium or substitutes ammonium salts thereof or mixtures thereof.
  • Ethylenediamine N,N'-disuccinic acids, especially the (S,S) isomer have been extensively described in U.S. Pat. No. 4,704,233, Nov. 3, 1987, to Hartman and Perkins.
  • Ethylenediamine N,N'-disuccinic acids is, for instance, commercially available under the tradename ssEDDS® from Palmer Research Laboratories.
  • Suitable amino carboxylates to be used herein include ethylene diamine terra acetates, diethylene triamine pentaacetates, diethylene triamine pentaacetate (DTPA),N- hydroxyethylethylenediamine triacetates, nitrilotri- acetates, ethylenediamine tetrapropionates, triethylenetetraaminehexa- acetates, ethanol-diglycines, propylene diamine tetracetic acid (PDTA) and methyl glycine di-acetic acid (MGDA), both in their acid form, or in their alkali metal, ammonium, and substituted ammonium salt forms.
  • PDTA propylene diamine tetracetic acid
  • MGDA methyl glycine di-acetic acid
  • Particularly suitable amino carboxylates to be used herein are diethylene triamine penta acetic acid, propylene diamine tetracetic acid (PDTA) which is, for instance, commercially available from BASF under the trade name Trilon FS® and methyl glycine di-acetic acid (MGDA).
  • PDTA propylene diamine tetracetic acid
  • MGDA methyl glycine di-acetic acid
  • carboxylate chelating agents to be used herein include salicylic acid, aspartic acid, glutamic acid, glycine, malonic acid or mixtures thereof.
  • Particularly preferred chelating agents to be used herein are amino aminotri(methylene phosphonic acid), di-ethylene-triamino-pentaacetic acid, diethylene triamine penta methylene phosphonate, 1-hydroxy ethane diphosphonate, ethylenediamine N,N'- disuccinic acid, and mixtures thereof.
  • compositions according to the present invention comprise up to 5%w/v of the total composition of a chelating agent, or mixtures thereof, preferably from 0.01 to 1.5%w/v and more preferably from 0.01 to 0.5%w/v.
  • compositions of the present invention may comprise a radical scavenger or a mixture thereof.
  • Suitable radical scavengers for use herein include the well-known substituted mono and dihydroxy benzenes and their analogs, alkyl and aryl carboxylates and mixtures thereof.
  • Preferred such radical scavengers for use herein include di-tert-butyl hydroxy toluene (BHT), hydroquinone, di-tert-butyl hydroqumone, mono- tert-butyl hydroquinone, tert-butyl-hydroxy anysole, benzoic acid, toluic acid, catechol, t-butyl catechol, benzylamine, l,l,3-tris(2-methyl-4- hydroxy-5-t-butylphenyl) butane, n-propyl- gallate or mixtures thereof and highly preferred is di-tert-butyl hydroxy toluene.
  • BHT di-tert-butyl hydroxy toluene
  • hydroquinone di-tert-butyl hydroqumone
  • mono- tert-butyl hydroquinone tert-butyl-hydroxy anysole
  • benzoic acid toluic acid
  • catechol t-butyl cate
  • radical scavengers like N-propyl-gallate may be commercially available from Nipa Laboratories under the trade name Nipanox SI®. Radical scavengers when used, are typically present herein in amounts ranging from up to 10%w/v of the total composition and preferably from 0.001 to 0.5%w/v.
  • compositions according to the present invention may further comprise an antioxidant or mixtures thereof.
  • the compositions herein comprise up to 10% by weight of the total composition of an antioxidant or mixtures thereof, preferably from 0.002 to 5%w/v, more preferably from 0.005 to 2%w/v, and most preferably from 0.01 to l%w/v.
  • Suitable antioxidants to be used herein include organic acids like citric acid, ascorbic acid, tartaric acid, adipic acid and sorbic acid, or amines like lecithin, or aminoacids like glutamine, methionine and cysteine, or esters like ascorbil paimitate, ascorbil stearate and triethylcitrate, or mixtures thereof.
  • Preferred antioxidants for use herein are citric acid, ascorbic acid, ascorbil paimitate, lecithin or mixtures thereof.
  • Such stabilising agent(s) may be present typically in an amount of 0 to 8 weight %, ideally 0.5 to 6 weight %, of the first aqueous composition.
  • the overall composition of the dispenser or each of the first and/or second aqueous compositions may further contain up to 25, 20, 15, 10, 5 or l%w/v of at least one component selected from a fragrance, inorganic salt, solvent, dye transfer inhibitors, water-soluble polymers, dye, germicide and preservative.
  • Water may be present in the overall composition of the dispenser in an amount of at least 50%w/v, more preferably at least 60%w/v of the composition or 0 to up to 100%w/v, preferably, 30 to 99%w/v or 50 to 99%w/v, more preferably, 50 to 90%w/v or 55 to 85%w/v, for example, 60 to 80%w/v of the composition.
  • 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 packaging to facilitate application of the composition to the fabric.
  • the packaging could comprise, a squez bottle, a roller ball applicator or a spray device.
  • An item of packaging containing the composition constitutes a further aspect of the invention, especially where the packaging item is transparent, given the light stability of the product.
  • 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.

Abstract

The present invention relates to stabilised aqueous compositions that contain hydrogen peroxide, an ethoxylated aliphatic phospono surfactant of formula: (I) (HO)(3-m)OP(R-(CH2-CH2-O)n-R1 )m or (HO)(3-m)OP(O-(CH2-CH2-O)n-R1 )m or (HO)(3-m)OP(O-R1-(CH2-CH2-0)n-H )m and at least one additional detersive surfactant.

Description

Aqueous Cleaning Compositions
The present invention relates to stabilised aqueous compositions that contain hydrogen peroxide, an ethoxylated aliphatic phospono surfactant of formula (I), at least one additional detersive surfactant.
One drawback to the use of hydrogen peroxide compositions is that without the use of a stabiliser, or a combination of stabilisers, the aqueous peroxide compositions characteristically decompose over a relatively short time period. The actual rate at which hydrogen peroxide compositions decompose will, of course, be dependent upon such factors as pH and the presence of trace amounts of various metal impurities, such as copper or chromium, which may act to catalytically decompose the same. Moreover, at moderately elevated temperatures, the rate of decomposition of such dilute hydrogen peroxide compositions is greatly accelerated.
An objective of the present invention is to provide a hydrogen peroxide containing composition that is stable to light, in particular TJV light. Preferably the product should also be physically stable, as well as chemically stable. Ideally the product is viscous 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 15 rpm). In addition, preferably, the product is transparent.
We present as a feature of the invention a cleaning composition comprising
a) hydrogen peroxide, b) a compound of formula (I)
(HO)(3-m)OP(R-(CH2-CH2-O)n-R1 )n or
(HO)(3-m)OP(O-(CH2-CH2-O)n-R1 )n or (HO)(3-m)OP(O-R1-(CH2-CH2-O)„-H )ra
wherein each n is independently an integer from 1 to 10; each R is independently a 1-14C alkylene or alkenylene chain; and R1 is 1-14C alkyl or alkenyl chain, provided that the total number of carbons in R and R1 does not exceed 20, preferably less than 16;
c) at least one additional detersive surfactant; and d) 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).
Hydrogen peroxide is commercially available in different grades, at 8%, 35% and 50%w/v active, and it is generally stabilised by the use of chelating agents. Preferred levels of hydrogen peroxide (as 100% active) are 0.1%w/v to 12%w/v, preferably from 2%w/v to 10%w/v, and ideally from 4%w/v to 9%w/v.
Examples of preferred detersive surfactants considered in this invention are either anionic or non-ionic surfactants and mixtures thereof. Preferred total levels of surfactant are from 1 to 50% w/v, ideally from 10 to 40%w/v and preferably 20 to 35%w/v.
The non-ionic surfactant is preferably a surfactant having a formula RO(CH2CH2O)nH wherein R is a saturated or unsaturated (preferably saturated) hydrocarbon chain ranging from C12 to C16 and n represents the number of repeating units and is a number of from 1 to 12. Examples of other non-ionic surfactants include higher aliphatic primary alcohols containing 12 to 16 carbon atoms which are condensed with three to thirteen moles of ethylene oxide.
Other examples of non-ionic surfactants include primary alcohol ethoxylates 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 Cll-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.
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 C10-20alkanol amides, the amide being a mono or di C2-4alkanolamine.
A preferred surfactant is an anionic surfactant. 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, alkylarnide sulfonates, alkylarylsulfonates, olefinsulfonates, paraffin sulfonates, alkyl sulfosuccinates, alkyl ether sulfosuccinates, alkylarnide sulfosuccinates, alkyl sulfosuccinamate, alkyl sulfoacetates, alkyl carboxylates, alkyl phosphates, alkyl ether phosphates, acyl sarconsinates, acyl isethionates, and N-acyl taurates. Generally, the alkyl or acyl radical in these various compounds comprise a carbon chain containing 12 to 20 carbon atoms.
Preferred surfactants are also alkyl naphthalene sulfonate anionic surfactants of the formula: R
Figure imgf000005_0001
wherein R is a straight chain or branched alkyl chain having from about 1 to about 25 carbon atoms, saturated or unsaturated, and the longest linear portion of the alkyl chain is 15 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 substituted ammonium cation.
Particularly preferred are alkyl sulfate anionic surfactants of the formula (II)
O
(π) II
RO -(CH2CH2O)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 thanl5 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.
In a preferred feature of the invention we have found that transparent viscous compositions of the invention are ideally formed from the combination of compounds of formula (I), (II) and C10-20alkanol amides, the amide is preferably a C 10-20 alkanolamide of a mono or di C2-4 alkanolamine.
We present as a further feature of the invention a cleaning composition comprising
a) a compound of formula (I); b) a compound of formula (II); c) a C 10-20alkanol amide, the amide is preferably a C 10-20 alkanolamide of a mono or di C2-4alkanolamine; d) hydrogen peroxide; and e) water.
The composition may include one or more further optional ingredients, such as buffers, inorganic salts, fragrance, chelating agents, dispersants, enzyme stabilisers, solvents, dye transfer inhibitors and polymers. The total amount of optional ingredients present in the composition is up to 25%w/v, ideally up to 20%w/v, or up to 15%w/v.
Suitable inorganic salts include metal oxides and halides, such as calcium chloride, for example.
Suitably pH buffers may be added to the composition in an amount of up to 5%w/v, suitable buffers include borate buffers.
Stabilising Agent Suitable stabilising agents include chelating agents, radical scavengers, antioxidants and mixtures of any thereof.
1. Chelating Agent
The compositions of the present invention may comprise a chelating agent or a mixture thereof as a preferred optional ingredient. Suitable chelating agents may be any of those known to those skilled in the art such as the ones selected from the group comprising phosphonate chelating agents, amino carboxylate chelating agents, other carboxylate chelating agents, polyfunctionally-substituted aromatic chelating agents, ethylenediamine N,N'-disuccinic acids, or mixtures thereof. The chelating agents inactivate the metal ions present on the surface of the fabrics and/or in the cleaning compositions (neat or diluted) that otherwise would contribute to the radical decomposition of any peroxygen bleach.
Suitable phosphonate chelating agents to be used herein may include alkali metal ethane 1-hydroxy diphosphonates (HEDP) also known as ethydronic acid, alkylene poly (alkylene phosphonate), as well as amino phosphonate compounds, including amino aminotri(methylene phosphonic acid) (ATMP), nitrilo trimethylene phosphonates (NTP), ethylene diamine terra methylene phosphonates, and diethylene triamine penta methylene phosphonates (DTPMP). The phosphonate compounds may be present either in their acid form or as salts of different cations on some or all of their acid functionalities. Preferred phosphonate chelating agents to be used herein are diethylene triamine penta methylene phosphonate (DTPMP) and ethane 1-hydroxy diphosphonate (HEDP or ethydronic acid). Such phosphonate chelating agents are commercially available from Monsanto under the trade name DEQUEST®.
Polyfunctionally-substituted aromatic chelating agents may also be useful in the compositions herein. See U.S. Pat. No. 3,812,044, issued May 21, 1974, to Connor et al. Preferred compounds of this type in acid form are dihydroxydisulfobenzenes such as 1,2- dihydroxy -3,5- disulfobenzene.
A preferred biodegradable chelating agent for use herein is ethylene diamine N,N'- disuccinic acid, or alkali metal, or alkaline earth, ammonium or substitutes ammonium salts thereof or mixtures thereof. Ethylenediamine N,N'-disuccinic acids, especially the (S,S) isomer have been extensively described in U.S. Pat. No. 4,704,233, Nov. 3, 1987, to Hartman and Perkins. Ethylenediamine N,N'-disuccinic acids is, for instance, commercially available under the tradename ssEDDS® from Palmer Research Laboratories. Suitable amino carboxylates to be used herein include ethylene diamine terra acetates, diethylene triamine pentaacetates, diethylene triamine pentaacetate (DTPA),N- hydroxyethylethylenediamine triacetates, nitrilotri- acetates, ethylenediamine tetrapropionates, triethylenetetraaminehexa- acetates, ethanol-diglycines, propylene diamine tetracetic acid (PDTA) and methyl glycine di-acetic acid (MGDA), both in their acid form, or in their alkali metal, ammonium, and substituted ammonium salt forms. Particularly suitable amino carboxylates to be used herein are diethylene triamine penta acetic acid, propylene diamine tetracetic acid (PDTA) which is, for instance, commercially available from BASF under the trade name Trilon FS® and methyl glycine di-acetic acid (MGDA).
Further carboxylate chelating agents to be used herein include salicylic acid, aspartic acid, glutamic acid, glycine, malonic acid or mixtures thereof.
Particularly preferred chelating agents to be used herein are amino aminotri(methylene phosphonic acid), di-ethylene-triamino-pentaacetic acid, diethylene triamine penta methylene phosphonate, 1-hydroxy ethane diphosphonate, ethylenediamine N,N'- disuccinic acid, and mixtures thereof.
Typically, the compositions according to the present invention comprise up to 5%w/v of the total composition of a chelating agent, or mixtures thereof, preferably from 0.01 to 1.5%w/v and more preferably from 0.01 to 0.5%w/v.
2. Radical Scavenger
The compositions of the present invention may comprise a radical scavenger or a mixture thereof. Suitable radical scavengers for use herein include the well-known substituted mono and dihydroxy benzenes and their analogs, alkyl and aryl carboxylates and mixtures thereof. Preferred such radical scavengers for use herein include di-tert-butyl hydroxy toluene (BHT), hydroquinone, di-tert-butyl hydroqumone, mono- tert-butyl hydroquinone, tert-butyl-hydroxy anysole, benzoic acid, toluic acid, catechol, t-butyl catechol, benzylamine, l,l,3-tris(2-methyl-4- hydroxy-5-t-butylphenyl) butane, n-propyl- gallate or mixtures thereof and highly preferred is di-tert-butyl hydroxy toluene. Such radical scavengers like N-propyl-gallate may be commercially available from Nipa Laboratories under the trade name Nipanox SI®. Radical scavengers when used, are typically present herein in amounts ranging from up to 10%w/v of the total composition and preferably from 0.001 to 0.5%w/v.
3. Antioxidant
The compositions according to the present invention may further comprise an antioxidant or mixtures thereof. Typically, the compositions herein comprise up to 10% by weight of the total composition of an antioxidant or mixtures thereof, preferably from 0.002 to 5%w/v, more preferably from 0.005 to 2%w/v, and most preferably from 0.01 to l%w/v.
Suitable antioxidants to be used herein include organic acids like citric acid, ascorbic acid, tartaric acid, adipic acid and sorbic acid, or amines like lecithin, or aminoacids like glutamine, methionine and cysteine, or esters like ascorbil paimitate, ascorbil stearate and triethylcitrate, or mixtures thereof. Preferred antioxidants for use herein are citric acid, ascorbic acid, ascorbil paimitate, lecithin or mixtures thereof.
Such stabilising agent(s) may be present typically in an amount of 0 to 8 weight %, ideally 0.5 to 6 weight %, of the first aqueous composition.
Other components
The overall composition of the dispenser or each of the first and/or second aqueous compositions may further contain up to 25, 20, 15, 10, 5 or l%w/v of at least one component selected from a fragrance, inorganic salt, solvent, dye transfer inhibitors, water-soluble polymers, dye, germicide and preservative.
Water
Water may be present in the overall composition of the dispenser in an amount of at least 50%w/v, more preferably at least 60%w/v of the composition or 0 to up to 100%w/v, preferably, 30 to 99%w/v or 50 to 99%w/v, more preferably, 50 to 90%w/v or 55 to 85%w/v, for example, 60 to 80%w/v of the composition. 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 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 constitutes 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 non-limiting examples
Figure imgf000010_0001
Figure imgf000011_0001

Claims

Claims
1. A cleaning composition comprising
a) hydrogen peroxide, b) a compound of formula (I)
(HO)(3-m)OP(R-(CH2-CH2-O)n-R1 )m or (HO)(3-m)OP(O-(CH2-CH2-O)n-R1 )m or (HO)(3-m)OP(O-R1-(CH2-CH2-O)n-H )m (1)
wherein each n is independently an integer from 1 to 10; each R is independently a 1-14C alkylene or alkenylene chain and each R1 is independently 1-14C alkyl or alkenyl chain, provided that the total number of carbons in R and R1 does not exceed 20; and wherein m is an integer from 1 to 3; and c) at least one additional detersive surfactant; and d) water.
A cleaning composition comprising
a) a compound of formula (I), as defined in claim 1 ; b) a compound of formula (II)
di) 1
RO-(CH2CH2O)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 15 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;
c) a C 10-20 alkanolamide, the amide is preferably a C 10-20 alkanolamide of a mono or di C2-4alkanolamine; and d) hydrogen peroxide, e) water.
3. A cleaning composition as claimed in either claim 1 or 2, wherein 0.1% w/v to 12% w/v of hydrogen peroxide (as 100% active) is present.
4. A cleaning composition as claimed in claim 1, wherein the additional detersive surfactant comprises a mixture of an anionic and a nonionic surfactant.
5. A transparent packaging item containing a composition as claimed in any claim from 1 to 4.
6. A method of treating stains on fabric which method comprises applying a composition as claimed in any claim from 1 to 4 to the stained fabric.
PCT/GB2004/000393 2003-01-31 2004-01-30 Aqueous cleaning compositions WO2004067194A2 (en)

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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007080187A1 (en) * 2006-01-13 2007-07-19 Aseptix Research B.V. Enhanced activity biocidal hyrogen peroxide composition
US7658953B2 (en) 2006-01-13 2010-02-09 Aseptix Research B.V. Enhanced activity biocidal hydrogen peroxide composition
US7879744B2 (en) 2007-08-30 2011-02-01 Kimberly-Clark Worldwide, Inc. Stabilized decolorizing composition
US8563017B2 (en) 2008-05-15 2013-10-22 Kimberly-Clark Worldwide, Inc. Disinfectant wet wipe
US8772218B2 (en) 2007-08-30 2014-07-08 Kimberly-Clark Worldwide, Inc. Stain-discharging and removing system
EP2597948B1 (en) 2010-07-27 2015-03-04 Buck-Chemie GmbH Adhesive acidic sanitary cleaning and deodorising product
WO2020205360A1 (en) 2019-04-02 2020-10-08 The Clorox Company Process for manufacturing multi-layer substrates comprising sandwich layers and polyethylene
US11472164B2 (en) 2018-12-21 2022-10-18 The Clorox Company Multi-layer substrates comprising sandwich layers and polyethylene

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2018237103A1 (en) * 2017-06-21 2018-12-27 The Procter & Gamble Company Fabric treatment

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3704262A (en) * 1970-03-19 1972-11-28 Gaf Corp Surfactant for electrolyte-containing processing solutions
US3741913A (en) * 1966-06-23 1973-06-26 Domsjo Ab Process for preparing spray dried detergent compositions
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
US4767558A (en) * 1985-08-05 1988-08-30 Colgate-Palmolive Company Low phosphate or phosphate free nonaqueous liquid nonionic laundry detergent composition and method of use
US4830764A (en) * 1986-10-27 1989-05-16 Sandoz Ltd. Polyoxyalkylene-containing phosphoric acid esters
EP0376704A1 (en) * 1988-12-28 1990-07-04 Unilever Plc Bleaching composition
EP0667392A2 (en) * 1994-02-14 1995-08-16 JEYES GROUP plc Bleach compositions
DE4418847A1 (en) * 1994-05-30 1995-12-07 Henkel Kgaa Bleaching and cleaning compsn.
EP0906404A2 (en) * 1996-06-13 1999-04-07 Henkel Kommanditgesellschaft auf Aktien Thickening agent for aqueous hydrogen peroxide solutions

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8929182D0 (en) * 1989-12-23 1990-02-28 Interox Chemicals Ltd Stabilisation

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3741913A (en) * 1966-06-23 1973-06-26 Domsjo Ab Process for preparing spray dried detergent compositions
US3704262A (en) * 1970-03-19 1972-11-28 Gaf Corp Surfactant for electrolyte-containing processing solutions
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
US4767558A (en) * 1985-08-05 1988-08-30 Colgate-Palmolive Company Low phosphate or phosphate free nonaqueous liquid nonionic laundry detergent composition and method of use
US4830764A (en) * 1986-10-27 1989-05-16 Sandoz Ltd. Polyoxyalkylene-containing phosphoric acid esters
EP0376704A1 (en) * 1988-12-28 1990-07-04 Unilever Plc Bleaching composition
EP0667392A2 (en) * 1994-02-14 1995-08-16 JEYES GROUP plc Bleach compositions
DE4418847A1 (en) * 1994-05-30 1995-12-07 Henkel Kgaa Bleaching and cleaning compsn.
EP0906404A2 (en) * 1996-06-13 1999-04-07 Henkel Kommanditgesellschaft auf Aktien Thickening agent for aqueous hydrogen peroxide solutions

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103266029A (en) * 2006-01-13 2013-08-28 阿塞普提克斯研究公司 Enhanced activity biocidal hyrogen peroxide composition
JP2009523155A (en) * 2006-01-13 2009-06-18 アセプティクス リサーチ ビー.ブイ. Enhanced activity biocidal hydrogen peroxide composition
US7658953B2 (en) 2006-01-13 2010-02-09 Aseptix Research B.V. Enhanced activity biocidal hydrogen peroxide composition
WO2007080187A1 (en) * 2006-01-13 2007-07-19 Aseptix Research B.V. Enhanced activity biocidal hyrogen peroxide composition
US8772218B2 (en) 2007-08-30 2014-07-08 Kimberly-Clark Worldwide, Inc. Stain-discharging and removing system
US7879744B2 (en) 2007-08-30 2011-02-01 Kimberly-Clark Worldwide, Inc. Stabilized decolorizing composition
US8563017B2 (en) 2008-05-15 2013-10-22 Kimberly-Clark Worldwide, Inc. Disinfectant wet wipe
EP2597948B1 (en) 2010-07-27 2015-03-04 Buck-Chemie GmbH Adhesive acidic sanitary cleaning and deodorising product
EP2597948B2 (en) 2010-07-27 2018-05-09 Buck-Chemie GmbH Adhesive acidic sanitary cleaning and deodorising product
US11472164B2 (en) 2018-12-21 2022-10-18 The Clorox Company Multi-layer substrates comprising sandwich layers and polyethylene
US11826989B2 (en) 2018-12-21 2023-11-28 The Clorox Company Multi-layer substrates comprising sandwich layers and polyethylene
US11858238B2 (en) 2018-12-21 2024-01-02 The Clorox Company Process for manufacturing multi-layer substrates comprising sandwich layers and polyethylene
WO2020205360A1 (en) 2019-04-02 2020-10-08 The Clorox Company Process for manufacturing multi-layer substrates comprising sandwich layers and polyethylene

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ES2268626T3 (en) 2007-03-16
AU2004208552A1 (en) 2004-08-12
WO2004067194A3 (en) 2004-11-18
DE602004002462D1 (en) 2006-11-02
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PL377993A1 (en) 2006-02-20

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