AU2004208552B2 - Aqueous cleaning compositions - Google Patents
Aqueous cleaning compositions Download PDFInfo
- Publication number
- AU2004208552B2 AU2004208552B2 AU2004208552A AU2004208552A AU2004208552B2 AU 2004208552 B2 AU2004208552 B2 AU 2004208552B2 AU 2004208552 A AU2004208552 A AU 2004208552A AU 2004208552 A AU2004208552 A AU 2004208552A AU 2004208552 B2 AU2004208552 B2 AU 2004208552B2
- Authority
- AU
- Australia
- Prior art keywords
- composition
- chain
- compound
- alkyl
- hydrogen peroxide
- Prior art date
- Legal status (The legal status 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 status listed.)
- Ceased
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3942—Inorganic per-compounds
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/65—Mixtures of anionic with cationic compounds
- C11D1/652—Mixtures of anionic compounds with carboxylic amides or alkylol amides
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/36—Organic compounds containing phosphorus
- C11D3/361—Phosphonates, phosphinates or phosphonites
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3947—Liquid compositions
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/29—Sulfates of polyoxyalkylene ethers
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/52—Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
- C11D1/523—Carboxylic alkylolamides, or dialkylolamides, or hydroxycarboxylic amides (R1-CO-NR2R3), where R1, R2 or R3 contain one hydroxy group per alkyl group
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Detergent Compositions (AREA)
Abstract
Aqueous compositions that contain hydrogen peroxide, at least one detersive surfactant and an ethoxylated aliphatic phosphono compound. The composition may comprise an ethoxylated alcohol, sodium lauryl sulphate, coconut diethanolamide, a dye, a fragrance, a chelant, and water. The composition is used as a stain remover for fabrics and is stable to light.
Description
Aqueous Cleaning Compositions The present invention relates to stabilised aqueous compositions that contain hydrogen peroxide, an ethoxylated aliphatic phospono surfactant of fornula (1), at least one 5 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 10 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. 15 The present invention desirably provides a hydrogen peroxide containing composition that is stable to light, in particular UV 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 20 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 25 a) hydrogen peroxide, b) a compound of formula (I)
(HO)(
3 -m)OP(R-(CH 2
-CH
2 -0).-R 1 )m or 30 (HO)( 3 -m)OP(0-(CH 2
-CH
2 -0).-R)m or WO 2004/067194 PCT/GB2004/000393 2
(HO)(
3 -m)OP(O-R-(CH 2
-CH
2 -0),-H )m wherein each n is independently an integer from 1 to 10; each R is independently a 1-1 4C alkylene or alkenylene chain; and R 1 is 1- 14C alkyl or alkenyl chain, provided that 5 the total number of carbons in R and R 1 does not exceed 20, preferably less than 16; c) at least one additional detersive surfactant; and d) water. 10 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 15 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 20 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 25 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. 30 Other examples of non-ionic surfactants include primary alcohol ethoxylates WO 2004/067194 PCT/GB2004/000393 3 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 5 foregoing type are C11-15 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, 10 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. 15 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 20 sulfates, alkyl benzene sulfates, alkyl benzene sulfonates, alkylaryl polyether sulfates, monoglyceride sulfates, alkylsulfonates, alkylamide sulfonates, alkylarylsulfonates, olefinsulfonates, paraffin sulfonates, alkyl sulfosuccinates, alkyl ether sulfosuccinates, alkylamide sulfosuccinates, alkyl sulfosuccinamate, alkyl sulfoacetates, alkyl carboxylates, alkyl phosphates, alkyl ether phosphates, acyl sarconsinates, acyl 25 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: WO 2004/067194 PCT/GB2004/000393 4 R
SO
3 M 5 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 10 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) 15 (II) 11
RO-(CH
2
CH
2 0)x -s -0-M 20 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 than15 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 25 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 30 formula (I), (II) and Cl 0-20alkanol amides, the amide is preferably a C10-20 5 alkanolamide of a mono or di C2-4 alkanolamine. We present as a further feature of the invention a cleaning composition comprising 5 a) a compound of formula (I); b) a compound of formula (II); c) a C10-20alkanol amide, the amide is preferably a C10-20 alkanolamide of a mono or di C2-4alkanolamine; d) hydrogen peroxide; and 10 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 15 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. 20 Suitably pH buffers may be added to the composition in an amount of up to 5%w/v, suitable buffers include borate buffers. The present invention provides a transparent packaging item containing a cleaning composition comprising 25 a) hydrogen peroxide, b) a compound of formula (I)
(HO)(
3 -)OP(R-(CH2-CH2-0)n-R 1 )m 30 or
(HO)(
3 -m)OP(O-(CH 2 -CH2-0)n-R )m 5A or
(HO)(
3 -m)OP(O-R-(CH 2
-CH
2 -0)nH)m (1) wherein each n is independently an integer from 1 to 10; each R is independently 5 a 1- 14C alkylene or alkenylene chain and each R' 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. 10 Throughout this specification the word "comprise", or variations such as "comprises" or "comprising", will be understood to imply the inclusion of a stated element, integer or step, or group of elements, integers or steps, but not the exclusion of any other element, integer or step, or group of elements, integers or steps. 15 Any discussion of documents, acts, materials, devices, articles or the like which has been included in the present specification is solely for the purpose of providing a context for the present invention. It is not to be taken as an admission that any or all of these matters form part of the prior art base or were common general knowledge in the 20 field relevant to the present invention as it existed before the priority date of each claim of this application. Stabilising Agent Suitable stabilising agents include chelating agents, radical scavengers, antioxidants and 25 mixtures of any thereof. 1. Chelating Agent The compositions of the present invention may comprise a chelating agent or a mixture 30 thereof as a preferred optional ingredient. Suitable chelating agents may be any of those WO 2004/067194 PCT/GB2004/000393 6 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 5 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 10 aminotri(methylene phosphonic acid) (ATMP), nitrilo trimethylene phosphonates (NTP), ethylene diamine tetra 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 15 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. 20 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 NN'-disuccinic acids, especially the 25 (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.
WO 2004/067194 PCT/GB2004/000393 7 Suitable amino carboxylates to be used herein include ethylene diamine tetra acetates, diethylene triamine pentaacetates, diethylene triamine pentaacetate (DTPA),N hydroxyethylethylenediamine triacetates, nitrilotri- acetates, ethylenediamine tetrapropionates, triethylenetetraaminehexa- acetates, ethanol-diglycines, propylene 5 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 10 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 15 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. 20 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 25 hydroxy toluene (BHT), hydroquinone, di-tert-butyl hydroquinone, mono- tert-butyl hydroquinone, tert-butyl-hydroxy anysole, benzoic acid, toluic acid, catechol, t-butyl catechol, benzylamine, 1,1,3-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 WO 2004/067194 PCT/GB2004/000393 8 Laboratories under the trade name Nipanox S 1@. Radical scavengers when used, are typically present herein in amounts ranging from up to 1 0%w/v of the total composition and preferably from 0.001 to 0.5 %w/v. 3. Antioxidant 5 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 1%w/v. Suitable antioxidants to be used herein include organic acids like citric acid, ascorbic 10 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 palmitate, lecithin or mixtures thereof 15 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 20 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 1%w/v of at least one component selected from a fragrance, inorganic salt, solvent, dye transfer inhibitors, water-soluble polymers, dye, germicide and preservative. 25 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 30 55 to 85%w/v, for example, 60 to 80%w/v of the composition.
WO 2004/067194 PCT/GB2004/000393 9 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 5 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 10 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. 15 The invention is illustrated by the following non-limiting examples %w/v %w/v Hydrogen Peroxide (50%) 7.5 5.5 Chelating Agent 0.12 0.12 Oxo Alcohol C13-C15 + 7EO 13 10.5 and 3EO - nonionic Compound of formula (I) 3.92 4.5 Compound of formula (I) 4.2 3.4 Coconut diethanolamide 3 1.5 Dye 0.001 0.001 Fragrance 0.3 0.25 Sodium hydroxide (48%) 0.5 0.4 Deionized Water 69.459 73.829 FINISHED PRODUCT 100 100 WO 2004/067194 PCT/GB2004/000393 10 STABILITY TEST Exposed to SUN LIGHT Packaging: Transparent PP bottle without UV filter Parameters time 0 1 week 2 w. 3 w. 4 w. 6 w. 8 w. pH 4.5 4.4 4.3 4.3 4.3 4.4 4.5 Viscosity 910 850 820 873 1200 1320 1250
H
2 0 2 7.50% 7.50% 7.50% 7.4% 7.40% 7.40% 7.40% Colour as ref. as ref. as ref. as ref. as ref. as ref. as ref.
Claims (6)
1. A transparent packaging item containing a cleaning composition comprising 5 a) hydrogen peroxide, b) a compound of formula (I) (HO)( 3 -m)OP(R-(CH 2 -CH 2 -0)n-RI )m or 10 (HO)( 3 -m)OP(O-(CH 2 -CH 2 -O)n-R' )m or (HO)( 3 -m)OP(0-R'-(CH 2 -CH 2 -O)n-H )m (1) wherein each n is independently an integer from I to 10; each R is 15 independently a 1-14C alkylene or alkenylene chain and each R' is independently 1-14C alkyl or alkenyl chain, provided that the total number of carbons in R and R' does not exceed 20; and wherein m is an integer from I to 3; and c) at least one additional detersive surfactant; and 20 d) water.
2. A transparent packaging item containing a cleaning composition comprising a) a compound of formula (I), as defined in claim 1; 25 b) a compound of formula (II) 0 II (II) RO-(CH 2 CH 2 0),-S-0-M 30| 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 806461_1.doc 12 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; 5 c) a C10-20 alkanolamide, the amide is preferably a C10-20 alkanolamide of a mono or di C2-4alkanolamine; and d) hydrogen peroxide. e) water. 10
3. A transparent packaging item as claimed in either claim I or 2, wherein the composition has 0.1% w/v to 12% w/v of hydrogen peroxide (as 100% active) present.
4. A transparent packaging item as claimed in claim 1, wherein the additional 15 detersive surfactant in the composition comprises a mixture of an anionic and a nonionic surfactant.
5. A method of treating stains on fabric which method comprises applying a composition as defined in any claim from I to 4 to the stained fabric. 20
6. A transparent packaging item substantially as hereinbefore described with reference to the examples and/or the preferred embodiments excluding, if any, comparative examples. 806461 1.doc
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0302245A GB2397823A (en) | 2003-01-31 | 2003-01-31 | Aqueous cleaning compositions |
| GB0302245.6 | 2003-01-31 | ||
| PCT/GB2004/000393 WO2004067194A2 (en) | 2003-01-31 | 2004-01-30 | Aqueous cleaning compositions |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2004208552A1 AU2004208552A1 (en) | 2004-08-12 |
| AU2004208552B2 true AU2004208552B2 (en) | 2009-05-28 |
Family
ID=9952193
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2004208552A Ceased AU2004208552B2 (en) | 2003-01-31 | 2004-01-30 | Aqueous cleaning compositions |
Country Status (8)
| Country | Link |
|---|---|
| EP (1) | EP1597342B1 (en) |
| AT (1) | ATE340234T1 (en) |
| AU (1) | AU2004208552B2 (en) |
| DE (1) | DE602004002462T2 (en) |
| ES (1) | ES2268626T3 (en) |
| GB (1) | GB2397823A (en) |
| PL (1) | PL377993A1 (en) |
| WO (1) | WO2004067194A2 (en) |
Families Citing this family (10)
| 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 |
| EP1987121B1 (en) * | 2006-01-13 | 2013-03-13 | Aseptix Research B.V. | Enhanced activity biocidal hyrogen peroxide composition |
| US8569221B2 (en) | 2007-08-30 | 2013-10-29 | 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 |
| DE102010032417A1 (en) | 2010-07-27 | 2012-02-02 | Buck- Chemie Gmbh | Acidic acid sanitary cleaning and fragrancing agent |
| WO2018237103A1 (en) * | 2017-06-21 | 2018-12-27 | The Procter & Gamble Company | Fabric treatment |
| US11364711B2 (en) | 2018-12-21 | 2022-06-21 | The Clorox Company | Multi-layer substrates comprising sandwich layers and polyethylene |
| MX2021011796A (en) | 2019-04-02 | 2021-10-13 | Clorox Co | Process for manufacturing multi-layer substrates comprising sandwich layers and polyethylene. |
| US12576176B2 (en) | 2021-10-07 | 2026-03-17 | The Clorox Company | Quat-based compostable and biodegradable premoistened cleaning and disinfecting wipes system |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1991009807A2 (en) * | 1989-12-23 | 1991-07-11 | Interox Chemicals Limited | Stabilisation of hydrogen peroxide solutions |
| 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 (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NO121968C (en) * | 1966-06-23 | 1977-06-13 | Mo Och Domsjoe Ab | |
| 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 |
| FR2605635B1 (en) * | 1986-10-27 | 1992-02-21 | Sandoz Sa | NOVEL PARTIAL PHOSPHORIC ACID ESTERS, THEIR PREPARATION AND THEIR USE FOR THE PRE-TREATMENT OF TEXTILE MATERIALS |
| GB8830296D0 (en) * | 1988-12-28 | 1989-02-22 | Unilever Plc | Bleaching composition |
| GB2286603B (en) * | 1994-02-14 | 1998-03-25 | Jeyes Group Plc | Bleach compositions |
-
2003
- 2003-01-31 GB GB0302245A patent/GB2397823A/en not_active Withdrawn
-
2004
- 2004-01-30 ES ES04706720T patent/ES2268626T3/en not_active Expired - Lifetime
- 2004-01-30 WO PCT/GB2004/000393 patent/WO2004067194A2/en not_active Ceased
- 2004-01-30 AT AT04706720T patent/ATE340234T1/en not_active IP Right Cessation
- 2004-01-30 DE DE602004002462T patent/DE602004002462T2/en not_active Expired - Lifetime
- 2004-01-30 EP EP04706720A patent/EP1597342B1/en not_active Expired - Lifetime
- 2004-01-30 AU AU2004208552A patent/AU2004208552B2/en not_active Ceased
- 2004-01-30 PL PL377993A patent/PL377993A1/en not_active Application Discontinuation
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1991009807A2 (en) * | 1989-12-23 | 1991-07-11 | Interox Chemicals Limited | Stabilisation of hydrogen peroxide solutions |
| 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 |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2004067194A3 (en) | 2004-11-18 |
| DE602004002462D1 (en) | 2006-11-02 |
| WO2004067194A2 (en) | 2004-08-12 |
| ES2268626T3 (en) | 2007-03-16 |
| ATE340234T1 (en) | 2006-10-15 |
| EP1597342A2 (en) | 2005-11-23 |
| AU2004208552A1 (en) | 2004-08-12 |
| PL377993A1 (en) | 2006-02-20 |
| GB0302245D0 (en) | 2003-03-05 |
| DE602004002462T2 (en) | 2007-09-13 |
| EP1597342B1 (en) | 2006-09-20 |
| GB2397823A (en) | 2004-08-04 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FGA | Letters patent sealed or granted (standard patent) | ||
| PC | Assignment registered |
Owner name: RECKITT BENCKISER VANISH B.V. Free format text: FORMER OWNER WAS: RECKITT BENCKISER N.V. |
|
| MK14 | Patent ceased section 143(a) (annual fees not paid) or expired |