EP0687727A1 - Bleaching compositions based on benzoyl peroxide and non ionic-surfactants mixture - Google Patents
Bleaching compositions based on benzoyl peroxide and non ionic-surfactants mixture Download PDFInfo
- Publication number
- EP0687727A1 EP0687727A1 EP94870098A EP94870098A EP0687727A1 EP 0687727 A1 EP0687727 A1 EP 0687727A1 EP 94870098 A EP94870098 A EP 94870098A EP 94870098 A EP94870098 A EP 94870098A EP 0687727 A1 EP0687727 A1 EP 0687727A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- fabrics
- composition
- composition according
- compositions
- bleaching
- 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.)
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- 239000000203 mixture Substances 0.000 title claims abstract description 104
- 238000004061 bleaching Methods 0.000 title claims abstract description 29
- 239000002736 nonionic surfactant Substances 0.000 title claims abstract description 28
- 239000004342 Benzoyl peroxide Substances 0.000 title 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 title 1
- 235000019400 benzoyl peroxide Nutrition 0.000 title 1
- 239000003093 cationic surfactant Substances 0.000 claims abstract description 18
- 239000007844 bleaching agent Substances 0.000 claims abstract description 16
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 5
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 37
- 239000004744 fabric Substances 0.000 claims description 26
- 235000013162 Cocos nucifera Nutrition 0.000 claims description 12
- 244000060011 Cocos nucifera Species 0.000 claims description 12
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 239000012190 activator Substances 0.000 claims description 6
- 239000012736 aqueous medium Substances 0.000 claims description 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 6
- 125000000963 oxybis(methylene) group Chemical group [H]C([H])(*)OC([H])([H])* 0.000 claims description 6
- MPNXSZJPSVBLHP-UHFFFAOYSA-N 2-chloro-n-phenylpyridine-3-carboxamide Chemical compound ClC1=NC=CC=C1C(=O)NC1=CC=CC=C1 MPNXSZJPSVBLHP-UHFFFAOYSA-N 0.000 claims description 5
- 239000000839 emulsion Substances 0.000 claims description 5
- 150000001450 anions Chemical group 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 3
- 125000002947 alkylene group Chemical group 0.000 claims description 3
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 3
- 239000004094 surface-active agent Substances 0.000 abstract description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract description 2
- 239000001301 oxygen Substances 0.000 abstract description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 230000002209 hydrophobic effect Effects 0.000 description 9
- 208000003251 Pruritus Diseases 0.000 description 8
- 239000004615 ingredient Substances 0.000 description 8
- 150000002978 peroxides Chemical class 0.000 description 8
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 7
- 230000007803 itching Effects 0.000 description 7
- 239000011734 sodium Substances 0.000 description 5
- 229910052708 sodium Inorganic materials 0.000 description 5
- 238000005406 washing Methods 0.000 description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
- 150000008051 alkyl sulfates Chemical class 0.000 description 4
- -1 hydroxyethyl groups Chemical group 0.000 description 4
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 4
- 239000002516 radical scavenger Substances 0.000 description 4
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- WEAPVABOECTMGR-UHFFFAOYSA-N triethyl 2-acetyloxypropane-1,2,3-tricarboxylate Chemical compound CCOC(=O)CC(C(=O)OCC)(OC(C)=O)CC(=O)OCC WEAPVABOECTMGR-UHFFFAOYSA-N 0.000 description 3
- YJHSJERLYWNLQL-UHFFFAOYSA-N 2-hydroxyethyl(dimethyl)azanium;chloride Chemical compound Cl.CN(C)CCO YJHSJERLYWNLQL-UHFFFAOYSA-N 0.000 description 2
- PRWJPWSKLXYEPD-UHFFFAOYSA-N 4-[4,4-bis(5-tert-butyl-4-hydroxy-2-methylphenyl)butan-2-yl]-2-tert-butyl-5-methylphenol Chemical compound C=1C(C(C)(C)C)=C(O)C=C(C)C=1C(C)CC(C=1C(=CC(O)=C(C=1)C(C)(C)C)C)C1=CC(C(C)(C)C)=C(O)C=C1C PRWJPWSKLXYEPD-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- ZTHYODDOHIVTJV-UHFFFAOYSA-N Propyl gallate Chemical compound CCCOC(=O)C1=CC(O)=C(O)C(O)=C1 ZTHYODDOHIVTJV-UHFFFAOYSA-N 0.000 description 2
- 244000299461 Theobroma cacao Species 0.000 description 2
- 235000009470 Theobroma cacao Nutrition 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 2
- 239000008280 blood Substances 0.000 description 2
- 210000004369 blood Anatomy 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 239000002304 perfume Substances 0.000 description 2
- 230000002441 reversible effect Effects 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 description 1
- DBRHJJQHHSOXCQ-UHFFFAOYSA-N 2,2-dihydroxyethyl(methyl)azanium;chloride Chemical compound [Cl-].C[NH2+]CC(O)O DBRHJJQHHSOXCQ-UHFFFAOYSA-N 0.000 description 1
- JIGUICYYOYEXFS-UHFFFAOYSA-N 3-tert-butylbenzene-1,2-diol Chemical compound CC(C)(C)C1=CC=CC(O)=C1O JIGUICYYOYEXFS-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
- 239000004435 Oxo alcohol Substances 0.000 description 1
- 240000003768 Solanum lycopersicum Species 0.000 description 1
- BGNXCDMCOKJUMV-UHFFFAOYSA-N Tert-Butylhydroquinone Chemical compound CC(C)(C)C1=CC(O)=CC=C1O BGNXCDMCOKJUMV-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 125000003435 aroyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- JBIROUFYLSSYDX-UHFFFAOYSA-M benzododecinium chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 JBIROUFYLSSYDX-UHFFFAOYSA-M 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000001589 carboacyl group Chemical group 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- CDJGWBCMWHSUHR-UHFFFAOYSA-M decyl(triethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCC[N+](CC)(CC)CC CDJGWBCMWHSUHR-UHFFFAOYSA-M 0.000 description 1
- RLGGVUPWOJOQHP-UHFFFAOYSA-M decyl-(2-hydroxyethyl)-dimethylazanium;chloride Chemical compound [Cl-].CCCCCCCCCC[N+](C)(C)CCO RLGGVUPWOJOQHP-UHFFFAOYSA-M 0.000 description 1
- 238000004851 dishwashing Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 150000005204 hydroxybenzenes Chemical class 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- VXBSKVAMQMBCCA-UHFFFAOYSA-M methyl sulfate;trimethyl(tetradecyl)azanium Chemical compound COS([O-])(=O)=O.CCCCCCCCCCCCCC[N+](C)(C)C VXBSKVAMQMBCCA-UHFFFAOYSA-M 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- ZWLPBLYKEWSWPD-UHFFFAOYSA-N o-toluic acid Chemical compound CC1=CC=CC=C1C(O)=O ZWLPBLYKEWSWPD-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 150000004965 peroxy acids Chemical class 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 235000010388 propyl gallate Nutrition 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 210000002374 sebum Anatomy 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical compound OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 1
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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/86—Mixtures of anionic, cationic, and non-ionic 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
- C11D1/66—Non-ionic compounds
- C11D1/835—Mixtures of non-ionic with cationic 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
- 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
- C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
- C11D1/146—Sulfuric acid esters
-
- 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
- C11D1/62—Quaternary ammonium 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
- C11D1/66—Non-ionic compounds
- C11D1/72—Ethers of polyoxyalkylene glycols
Definitions
- the present invention relates to bleaching compositions.
- the compositions herein are particularly useful for the bleaching of fabrics.
- compositions for the bleaching of laundry have been extensively described in the art.
- Bleaching compositions can be classified into peroxide bleaching compositions and hypochlorite bleaching compositions.
- Peroxide bleaching compositions have the advantage over hypochlorite bleaching compositions that they are generally considered as being somewhat safer to fabrics, specifically to colored fabrics.
- Peroxide compositions however have the inconveniency that they are often chemically unstable, which makes it difficult to formulate peroxide bleaching compositions which are sufficiently stable to be commercialized.
- a possible solution to this problem consists in formulating compositions with a high level of peroxide, to extend the "effective" period of the composition.
- compositions may reach the user which still comprise a high amount of peroxide, whereby possible skin itching may occur if the user's skin comes in contact with the peroxide composition, before or during use.
- This itching phenomenon is quite moderate and fully reversible, but is does constitute potential discomfort for the user.
- composition comprising a peroxygen bleach in lower amounts, i.e. in amounts where substantially no itching occurs, and which yet remain effective in bleaching fabrics.
- an aqueous composition comprising, in addition to lower amounts of peroxygen bleach, a water-soluble cationic surfactant in combination with a hydrophilic nonionic surfactant.
- compositions of the present invention comprise hydrogen peroxide or a source thereof, a cationic surfactant according to the formula R1R2R3R4N+X-, where R1 is C8-C16 alkyl or is R5-T-CO-R6, wherein T is O, NH or N-C1-C4 alkyl, R5 is a divalent C1-C3 alkylene group or (C2H4O)m, wherein m is from 1 to 8, wherein each of R2,R3,R4 is independently C1-C4 alkyl or hydroxy alkyl, benzyl, or (C2H4O)xH where x is from 2 to 5, not more than one of R2,R3,R4 being benzyl, and X is an anion, said composition further comprising a hydrophilic nonionic surfactant having an HLB above 13.
- compositions according to the present invention are peroxide bleaching compositions.
- the compositions herein comprise hydrogen peroxide or a source thereof.
- a problem which may occur with compositions comprising hydrogen peroxide above a certain level is that the skin of the user which comes in contact with the composition may itch. This itching phenomenon is harmless and quickly fully reversible, but it may nevertheless cause discomfort to the user.
- This problem will not occur directly if the composition comprises a hydrogen peroxide source instead of hydrogen peroxide per se, but it may occur upon use, when the composition is diluted in water before use and hydrogen peroxide is then formed.
- the compositions herein thus comprise hydrogen peroxide or a source thereof in amounts not causing any skin itching.
- Suitable sources of hydrogen peroxyde for use herein include perborates, percarbonates, persulfates and the like. It is preferred however to use hydrogen peroxide per se, and the compositions herein will comprise from 1% to 10% by weight of the total composition of hydrogen peroxide, preferably from 2% to 4%. Indeed, we have found that, when used in higher amounts, skin itching phenomenon start to appear.
- compositions herein comprise a cationic surfactant according to the formula R1R2R3R4N+X-, where R1 is C8-C16 alkyl or is R5-T-CO-R6, wherein T is O, NH or N-C1-C4 alkyl, R5 is a divalent C1-C3 alkylene group or (C2H4O)m, wherein m is from 1 to 8, wherein each of R2,R3,R4 is independently C1-C4 alkyl or hydroxy alkyl, benzyl, or (C2H4O)xH where x is from 2 to 5, not more than one of R2,R3,R4 being benzyl, and X is an anion. It is of course possible to use herein mixtures of different cationic surfactants according to the formula hereinabove.
- Preferred alkyl chain length for R1 is C12-15, particularly where the alkyl group is a mixture of chain length derived from coconut or palm kernel fat or is derived synthetically by olefin build up or OXO alcohol synthesis.
- Preferred groups for R2,R3 and R4 are methyl and hydroxyethyl groups and suitable anion X include halide, methosulfate, acetate and phosphate ions.
- Suitable cationic surfactant for use herein are: coconut trimethyl ammonium chloride, preferred for use herein, or bromide as Cequartyl ® from Rhone Poulenc and Empigen ® 5141 from Albright & Wilson, coconut methyl dihydroxyethyl ammonium chloride or bromide, decyl triethyl ammonium chloride, decyl dimethyl hydroxyethyl ammonium chloride or bromide, C12-15 dimethyl hydroxyethyl ammonium chloride or bromide, coconut dimethyl hydroxyethyl ammonium chloride or bromide, myristyl trimethyl ammonium methyl sulfate, lauryl dimethyl benzyl ammonium chloride or bromide as Bacforbl ® 80 from Sidobre, Sinove ® and Bardac ® 205 M from Lonza. lauryl dimethyl (ethenoxy)4 ammonium chloride or bromide.
- compositions herein comprise from 0.1% to 20% by weight of the total composition of said cationic surfactants, or mixtures thereof, preferably from 1% to 5%.
- the compositions herein comprise a hydrophilic nonionic surfactant.
- suitable nonionic surfactants for use herein are those having an HLB above 13. It is of course possible to use mixtures of said nonionic surfactants.
- a wide variety of nonionic surfactants are commercially available. Typically, nonionic surfactants are alkoxylated fatty alcohols. And the HLB of a given nonionic surfactant depends on the chain length of the fatty alcohol, the nature of the alkoxylating group as well as the degree of alkoxylation.
- Surfactant catalogs are available which list nonionic surfactants with their corresponding HLBs. Suitable for use herein are those which have an HLB of above 13.
- Such nonionic surfactants are commercially available for instance under the trade name Dobanol ®, 91-8, 91-9, 91-10 and 91-12, all from Shell.
- compositions herein should comprise from 0.1% to 20% by weight of the total composition, preferably from 2% to 10% of said hydrophilic nonionic surfactant or mixtures thereof.
- said cationic surfactant and said hydrophilic nonionic surfactant should be present in a weight ratio of cationic to nonionic of about 1:3.
- the compositions herein can be advantageously formulated as emulsions comprising two nonionic surfactants with different HLBs. Indeed, by formulating in an aqueous medium at least two different nonionic surfactants having different HLBs, a stable emulsion can be obtained.
- compositions herein comprise at least one hydrophilic nonionic surfactant, which can be the nonionic surfactant described herein before, and a more hydrophobic nonionic surfactant.
- Suitable hydrophobic surfactants to form the hydrophobic phase of the emulsion typically have an HLB of less than about 9.
- the compositions of this embodiment can be made by mixing together all the hydrophilic ingredients, i.e. water, said hydrophilic nonionic surfactant, said cationic surfactant and all other hydrophilic ingredients such as dyes, optical brighteners.
- hydrophobic ingredients are mixed, i.e. said hydrophobic nonionic surfactant together with other, optional, hydrophobic ingredients which are to be formulated in the composition, such as perfumes, solvents, enzymes, bleach activators and polymers. Then, both mixtures are mixed together.
- a bleach activator i.e. a peracid precursor
- a suitable hydrophobic bleach activator for use herein includes acetyl triethyl citrate, as described in WO 93/12067, as well as compounds according to the formula R-O-O-R' where R and R' are independently alkyl, alkenyl, alkanoyl, aryl, aroyl, alkylaryl or alkylaroyl radicals.
- the pH of the compositions herein plays a role in the chemical stability of the composition. Accordingly, the compositions herein are preferably formulated at a pH of from 1 to 7, preferably 3 to 5.
- suitable means can be used for adjusting the pH of the compositions, including organic or inorganic acids, alkanolamines and the like. It may be desirable to use alkanolamines herein, as we have found that alkanolamines have an effect on the viscosity of the product, and thus can be used as viscosity regulators, if necessary.
- compositions herein may comprise a variety of optional ingredients.
- a preferred optional feature of the compositions herein is the presence of radical scavengers, which are beneficial to the stability of the compositions herein.
- Suitable radical scavengers for use herein include the well known substituted mono and di hydroxy benzenes and their analogs, alkyl and aryl carboxylates, and mixtures thereof.
- Preferred radical scavengers for use herein include butyl hydroxy toluene, mono-tert-butyl hydroquinone, benzoic acid, toluic acid, t-butyl catechol, benzylamine, 1,1,3-tris(2-methyl-4-hydroxy-5-t-butylphenyl) butane, commercially available under the trade name Topanol CA ® ex ICI, as well as n-propyl-gallate.
- Radical scavengers when used, are typically present herein in amounts ranging from 0.01% to 2% by weight of the total composition, preferably 0.01% to 0.2%.
- compositions herein may further comprise other optionals, including anionic and cationic surfactants, to be formulated in the hydrophilic phase herein, builders and chelants, as well as aesthetics, including dyes and perfumes and the like.
- compositions according to the present invention are useful as laundry bleaches, including for the pretreatment of stains on laundry items prior washing. Indeed, pretreatment of fabrics before washing allows a close contact of the product with the stains, and the bleaching mechanism described herein occurs at a later stage, when the pretreated fabrics are contacted with warm water.
- the compositions herein can also be formulated as detergent compositions per se, or as detergency additives, to be used in addition to a detergent.
- Compositions herein can further be used as dishwashing compositions, or as hard surface cleaners, provided that contact with warm water occurs at some point in time in the washing process.
- the present invention further encompasses a process of bleaching fabrics, dishes or hard surfaces wherein said fabrics, dishes or hard surfaces are contacted with a bleaching liquor comprising a composition according to any of the preceding claims in an aqueous medium at a temperature of from 30°C to 90°C, and said bleaching liquor is subsequently rinsed off of said fabrics, dishes or hard surfaces.
- the composition described herein is first applied to fabrics, as a so-called pretreater, preferably to the stained portions of said fabrics, and said pretreated fabrics are subsequently contacted with an aqueous medium at a temperature of from 30°C to 70°C, for a period of time sufficient to bleach said fabrics.
- said bleaching liquor is formed at the time the fabrics are introduced in said aqueous medium. Subsequently, said bleaching liquor is rinsed off of said fabrics.
- composition 1 Dobanol ® 91-8 3% Coconut trimethyl ammonium chloride 1% H2O2 4% Sodium Coconut Alkyl Sulfate 10% Dobanol ® 23-3 5% Water and minors to balance pH 4
- Composition 2 Dobanol ® 91-8 3% Coconut trimethyl ammonium chloride 1% H2O2 4% Sodium Coconut Alkyl Sulfate 4% Dobanol ® 23-3 10% Water and minors to balance pH 4
- Composition 3 Dobanol ® 91-10 3% Coconut trimethyl ammonium chloride 1% H2O2 4% Sodium Coconut Alkyl Sulfate 2% Dobanol ® 23-3 7% Water and minors to balance pH 4
- Composition 4 Dobanol 91-8 3% Bardac ® 205M 1% H2O2 4% Sodium Coconut Alkyl Sulfate 2% Dobanol ® 23-3 7% Water and minors to balance pH 4
- Composition 4 Dobanol 91-8
- the present invention concerns the incorporation of a specific cationic/nonionic surfactant system in a liquid peroxygen bleaching composition which allows to reduce the amount of peroxygen bleach without losing performance.
- the technical data below illustrate the present invention.
- the tests are made with the following conditions. The tests are performed on cotton fabrics, with 6 replicates per test. The fabrics are stained as indicated hereinabove, and 0.2g of prototype is applied to the stains, prior to washing. Then the fabrics are washed in a Launder-O-meter, with 5 g of Dash Ultra Powder in 500 ml water. There is no waiting period between application of the prototype on the stains, and the subsequent washing.
- Prototype A is a composition as composition 1 hereinabove, but without Dobanol 91-8 and without cationic surfactant.
- Prototype B is the same as Prototype A, but with 7% level instead of 4%. The results are listed in the table below. Stains Prototype 1 vs. Prototype B 40° C Comp. 1 vs. Prototype B 40° C Prototype A vs. Prototype B 60° C Comp. 1 vs.
- Prototype B 60° C Grass -0.8 s -0.2 -1.0 s -0.3 Cocoa +0.1 +0.3 -0.9 0.0 Tea -0.4 -0.4 -0.7 -0.2 Wine -0.8 -0.3 -0.7 s 0.0 Vegetal Oil -1.0 s +0.1 -1.0 s 0.0 Blood -3.2 s -1.7 s -4.0 s -0.8 s
- composition 2 exemplified hereinbefore is compared to a reference composition.
- composition according to the present invention performs better than an activated bleaching composition comprising a higher amount of hydrogen peroxide.
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Abstract
Description
- The present invention relates to bleaching compositions. The compositions herein are particularly useful for the bleaching of fabrics.
- Compositions for the bleaching of laundry have been extensively described in the art. Bleaching compositions can be classified into peroxide bleaching compositions and hypochlorite bleaching compositions. Peroxide bleaching compositions have the advantage over hypochlorite bleaching compositions that they are generally considered as being somewhat safer to fabrics, specifically to colored fabrics. Peroxide compositions however have the inconveniency that they are often chemically unstable, which makes it difficult to formulate peroxide bleaching compositions which are sufficiently stable to be commercialized. A possible solution to this problem consists in formulating compositions with a high level of peroxide, to extend the "effective" period of the composition. A possible drawback of this solution is that compositions may reach the user which still comprise a high amount of peroxide, whereby possible skin itching may occur if the user's skin comes in contact with the peroxide composition, before or during use. This itching phenomenon is quite moderate and fully reversible, but is does constitute potential discomfort for the user.
- It is thus an object of the present invention to formulate a composition comprising a peroxygen bleach in lower amounts, i.e. in amounts where substantially no itching occurs, and which yet remain effective in bleaching fabrics.
- It has now been found that this object could be met by formulating an aqueous composition comprising, in addition to lower amounts of peroxygen bleach, a water-soluble cationic surfactant in combination with a hydrophilic nonionic surfactant.
- The compositions of the present invention comprise hydrogen peroxide or a source thereof, a cationic surfactant according to the formula R1R2R3R4N+X-, where R1 is C8-C16 alkyl or is R5-T-CO-R6, wherein T is O, NH or N-C1-C4 alkyl, R5 is a divalent C1-C3 alkylene group or (C2H4O)m, wherein m is from 1 to 8, wherein each of R2,R3,R4 is independently C1-C4 alkyl or hydroxy alkyl, benzyl, or (C2H4O)xH where x is from 2 to 5, not more than one of R2,R3,R4 being benzyl, and X is an anion, said composition further comprising a hydrophilic nonionic surfactant having an HLB above 13.
- The compositions according to the present invention are peroxide bleaching compositions. Thus the compositions herein comprise hydrogen peroxide or a source thereof. As discussed hereinbefore, a problem which may occur with compositions comprising hydrogen peroxide above a certain level, is that the skin of the user which comes in contact with the composition may itch. This itching phenomenon is harmless and quickly fully reversible, but it may nevertheless cause discomfort to the user. This problem will not occur directly if the composition comprises a hydrogen peroxide source instead of hydrogen peroxide per se, but it may occur upon use, when the composition is diluted in water before use and hydrogen peroxide is then formed. The compositions herein thus comprise hydrogen peroxide or a source thereof in amounts not causing any skin itching.
- Suitable sources of hydrogen peroxyde for use herein include perborates, percarbonates, persulfates and the like. It is preferred however to use hydrogen peroxide per se, and the compositions herein will comprise from 1% to 10% by weight of the total composition of hydrogen peroxide, preferably from 2% to 4%. Indeed, we have found that, when used in higher amounts, skin itching phenomenon start to appear.
- Because the level of hydrogen peroxide, or source thereof, is reduced, there would result a poorer bleaching performance, compared to compositions with higher amounts of peroxygen bleach which in turn might cause skin itching. We have found that the bleaching performance at higher temperatures, e.g. as from 50°C could be maintained, even with lower amounts of peroxygen bleach, by formulating a specific surfactant system comprising a narrowly-defined cationic surfactant as well as a narrowly-defined hydrophilic nonionic surfactant.
- Accordingly, the compositions herein comprise a cationic surfactant according to the formula R1R2R3R4N+X-, where R1 is C8-C16 alkyl or is R5-T-CO-R6, wherein T is O, NH or N-C1-C4 alkyl, R5 is a divalent C1-C3 alkylene group or (C2H4O)m, wherein m is from 1 to 8, wherein each of R2,R3,R4 is independently C1-C4 alkyl or hydroxy alkyl, benzyl, or (C2H4O)xH where x is from 2 to 5, not more than one of R2,R3,R4 being benzyl, and X is an anion. It is of course possible to use herein mixtures of different cationic surfactants according to the formula hereinabove.
- Preferred alkyl chain length for R1 is C12-15, particularly where the alkyl group is a mixture of chain length derived from coconut or palm kernel fat or is derived synthetically by olefin build up or OXO alcohol synthesis. Preferred groups for R2,R3 and R4 are methyl and hydroxyethyl groups and suitable anion X include halide, methosulfate, acetate and phosphate ions.
- Examples of suitable cationic surfactant for use herein are:
coconut trimethyl ammonium chloride, preferred for use herein, or bromide as Cequartyl ® from Rhone Poulenc and Empigen ® 5141 from Albright & Wilson,
coconut methyl dihydroxyethyl ammonium chloride or bromide,
decyl triethyl ammonium chloride,
decyl dimethyl hydroxyethyl ammonium chloride or bromide,
C12-15 dimethyl hydroxyethyl ammonium chloride or bromide,
coconut dimethyl hydroxyethyl ammonium chloride or bromide,
myristyl trimethyl ammonium methyl sulfate,
lauryl dimethyl benzyl ammonium chloride or bromide as Bacforbl ® 80 from Sidobre, Sinove ® and Bardac ® 205 M from Lonza.
lauryl dimethyl (ethenoxy)4 ammonium chloride or bromide. - The compositions herein comprise from 0.1% to 20% by weight of the total composition of said cationic surfactants, or mixtures thereof, preferably from 1% to 5%.
- As a further essential ingredient, the compositions herein comprise a hydrophilic nonionic surfactant. We have found that the suitable nonionic surfactants for use herein are those having an HLB above 13. It is of course possible to use mixtures of said nonionic surfactants. A wide variety of nonionic surfactants are commercially available. Typically, nonionic surfactants are alkoxylated fatty alcohols. And the HLB of a given nonionic surfactant depends on the chain length of the fatty alcohol, the nature of the alkoxylating group as well as the degree of alkoxylation. Surfactant catalogs are available which list nonionic surfactants with their corresponding HLBs. Suitable for use herein are those which have an HLB of above 13. Such nonionic surfactants are commercially available for instance under the trade name Dobanol ®, 91-8, 91-9, 91-10 and 91-12, all from Shell.
- The compositions herein should comprise from 0.1% to 20% by weight of the total composition, preferably from 2% to 10% of said hydrophilic nonionic surfactant or mixtures thereof. In a preferred embodiment of the present invention, said cationic surfactant and said hydrophilic nonionic surfactant should be present in a weight ratio of cationic to nonionic of about 1:3.
The compositions herein can be advantageously formulated as emulsions comprising two nonionic surfactants with different HLBs. Indeed, by formulating in an aqueous medium at least two different nonionic surfactants having different HLBs, a stable emulsion can be obtained. This emulsion can then be used to formulate, in a single composition, different ingredients which are otherwise poorly compatible, e.g. a bleach activator with hydrogen peroxide. In this embodiment of the invention the compositions herein comprise at least one hydrophilic nonionic surfactant, which can be the nonionic surfactant described herein before, and a more hydrophobic nonionic surfactant. Suitable hydrophobic surfactants to form the hydrophobic phase of the emulsion typically have an HLB of less than about 9. The compositions of this embodiment can be made by mixing together all the hydrophilic ingredients, i.e. water, said hydrophilic nonionic surfactant, said cationic surfactant and all other hydrophilic ingredients such as dyes, optical brighteners. Separately, all hydrophobic ingredients are mixed, i.e. said hydrophobic nonionic surfactant together with other, optional, hydrophobic ingredients which are to be formulated in the composition, such as perfumes, solvents, enzymes, bleach activators and polymers. Then, both mixtures are mixed together. If the composition comprises a bleach activator, i.e. a peracid precursor, it is preferable to choose a hydrophobic bleach activator which can be formulated in said hydrophobic mixture, and thus remains separated from the hydrophilic peroxygen bleach. This adds to the chemical stability of the compositions, thus its performance as more oxygen remains available throughout time. A suitable hydrophobic bleach activator for use herein includes acetyl triethyl citrate, as described in WO 93/12067, as well as compounds according to the formula R-O-O-R' where R and R' are independently alkyl, alkenyl, alkanoyl, aryl, aroyl, alkylaryl or alkylaroyl radicals. - We have observed that the pH of the compositions herein plays a role in the chemical stability of the composition. Accordingly, the compositions herein are preferably formulated at a pH of from 1 to 7, preferably 3 to 5. A variety of suitable means can be used for adjusting the pH of the compositions, including organic or inorganic acids, alkanolamines and the like. It may be desirable to use alkanolamines herein, as we have found that alkanolamines have an effect on the viscosity of the product, and thus can be used as viscosity regulators, if necessary.
- The compositions herein may comprise a variety of optional ingredients. A preferred optional feature of the compositions herein is the presence of radical scavengers, which are beneficial to the stability of the compositions herein. Suitable radical scavengers for use herein include the well known substituted mono and di hydroxy benzenes and their analogs, alkyl and aryl carboxylates, and mixtures thereof. Preferred radical scavengers for use herein include butyl hydroxy toluene, mono-tert-butyl hydroquinone, benzoic acid, toluic acid, t-butyl catechol, benzylamine, 1,1,3-tris(2-methyl-4-hydroxy-5-t-butylphenyl) butane, commercially available under the trade name Topanol CA ® ex ICI, as well as n-propyl-gallate. Radical scavengers, when used, are typically present herein in amounts ranging from 0.01% to 2% by weight of the total composition, preferably 0.01% to 0.2%.
- The compositions herein may further comprise other optionals, including anionic and cationic surfactants, to be formulated in the hydrophilic phase herein, builders and chelants, as well as aesthetics, including dyes and perfumes and the like.
- The compositions according to the present invention are useful as laundry bleaches, including for the pretreatment of stains on laundry items prior washing. Indeed, pretreatment of fabrics before washing allows a close contact of the product with the stains, and the bleaching mechanism described herein occurs at a later stage, when the pretreated fabrics are contacted with warm water. The compositions herein can also be formulated as detergent compositions per se, or as detergency additives, to be used in addition to a detergent. Compositions herein can further be used as dishwashing compositions, or as hard surface cleaners, provided that contact with warm water occurs at some point in time in the washing process.
- The present invention further encompasses a process of bleaching fabrics, dishes or hard surfaces wherein said fabrics, dishes or hard surfaces are contacted with a bleaching liquor comprising a composition according to any of the preceding claims in an aqueous medium at a temperature of from 30°C to 90°C, and said bleaching liquor is subsequently rinsed off of said fabrics, dishes or hard surfaces. In one embodiment of this process, the composition described herein is first applied to fabrics, as a so-called pretreater, preferably to the stained portions of said fabrics, and said pretreated fabrics are subsequently contacted with an aqueous medium at a temperature of from 30°C to 70°C, for a period of time sufficient to bleach said fabrics. In this embodiment, said bleaching liquor is formed at the time the fabrics are introduced in said aqueous medium. Subsequently, said bleaching liquor is rinsed off of said fabrics.
- The present invention is further illustrated by the following examples and data.
- The following formulations according to the present invention are made by mixing the listed ingredients in the listed proportions (in weight %).
Composition 1 Dobanol ® 91-8 3% Coconut trimethyl ammonium chloride 1% H2O2 4% Sodium Coconut Alkyl Sulfate 10% Dobanol ® 23-3 5% Water and minors to balance pH 4 Composition 2 Dobanol ® 91-8 3% Coconut trimethyl ammonium chloride 1% H2O2 4% Sodium Coconut Alkyl Sulfate 4% Dobanol ® 23-3 10% Water and minors to balance pH 4 Composition 3 Dobanol ® 91-10 3% Coconut trimethyl ammonium chloride 1% H2O2 4% Sodium Coconut Alkyl Sulfate 2% Dobanol ® 23-3 7% Water and minors to balance pH 4 Composition 4 Dobanol 91-8 3% Bardac ® 205M 1% H2O2 4% Sodium Coconut Alkyl Sulfate 2% Dobanol ® 23-3 5% Water and minors to balance pH 4 - The present invention concerns the incorporation of a specific cationic/nonionic surfactant system in a liquid peroxygen bleaching composition which allows to reduce the amount of peroxygen bleach without losing performance. The technical data below illustrate the present invention. The tests are made with the following conditions. The tests are performed on cotton fabrics, with 6 replicates per test. The fabrics are stained as indicated hereinabove, and 0.2g of prototype is applied to the stains, prior to washing. Then the fabrics are washed in a Launder-O-meter, with 5 g of Dash Ultra Powder in 500 ml water. There is no waiting period between application of the prototype on the stains, and the subsequent washing.
- Prototype A is a composition as composition 1 hereinabove, but without Dobanol 91-8 and without cationic surfactant. Prototype B is the same as Prototype A, but with 7% level instead of 4%. The results are listed in the table below.
Stains Prototype 1 vs. Prototype B 40° C Comp. 1 vs. Prototype B 40° C Prototype A vs. Prototype B 60° C Comp. 1 vs. Prototype B 60° C Grass -0.8 s -0.2 -1.0 s -0.3 Cocoa +0.1 +0.3 -0.9 0.0 Tea -0.4 -0.4 -0.7 -0.2 Wine -0.8 -0.3 -0.7 s 0.0 Vegetal Oil -1.0 s +0.1 -1.0 s 0.0 Blood -3.2 s -1.7 s -4.0 s -0.8 s - The results are expressed as panel score units as evaluated by expert judges. Comparing Prototype A vs Prototype B shows that a decrease in H2O2 leads to a loss of performance. Comparing Composition 1 vs Composition B shows that Composition 1 is as good as prototype B, even though it has about half less H2O2.
- Another test is performed as in the previous experiment. In this test, composition 2 exemplified hereinbefore is compared to a reference composition. The reference is an activated bleaching composition comprising hydrogen peroxide and acetyl triethyl citrate. More specifically, the formulation comprises 6% H2O2, 3.5% acetyl triethyl citrate, 6% Lutensol ® TO3, 8% Dobanol ® 45-7, 1.5% Sodium Alkyl Sulfate, 0.3% Citric Acid, 0.2%, water to balance, pH=4).
-
40° C 60° C Grass + 0.2 0.0 Cocoa +0.0 +0.2 Tea -0.6 -0.2 Wine -0.1 0.0 Vegetal Oil -0.5 -0.5 Mineral Oil +0.3 +0.3 Make Up +0.92s +0.9s Tomato +0.92s +0.4 Sebum -0.67 +0.5 Blood -1.0s -4.0 s - This comparison shows that a composition according to the present invention performs better than an activated bleaching composition comprising a higher amount of hydrogen peroxide.
Claims (10)
- A composition comprising hydrogen peroxide or a source thereof, a cationic surfactant according to the formula R1R2R3R4N+X-, or mixtures thereof, where R1 is C8-C16 alkyl or is R5-T-CO-R6, wherein T is O, NH or N-C1-C4 alkyl, R5 is a divalent C1-C3 alkylene group or (C2H4O)m, wherein m is from 1 to 8, wherein each of R2,R3,R4 is independently C1-C4 alkyl or hydroxy alkyl, benzyl, or (C2H4O)xH where x is from 2 to 5, not more than one of R2,R3,R4 being benzyl, and X is an anion, said composition further comprising a hydrophilic nonionic surfactant having an HLB above 13, or mixtures thereof.
- A composition according to claim 1 which comprises hydrogen peroxide, in amounts of from 1 % to 10% by weight of the total composition, preferably from 2% to 4%.
- A composition according to the preceding claims which comprises from 0.1% to 20% by weight of the total composition of said cationic surfactants, or mixtures thereof, preferably from 1% to 5%.
- A composition according to the preceding claims wherein said cationic surfactant is coconut trimethyl ammonium chloride.
- A composition according to the preceding claims which comprises from 0.1% to 20% by weight of the total composition of said nonionic surfactant, or mixtures thereof, preferably from 2% to 10%.
- A composition according to the preceding claims where said cationic surfactant and said hydrophilic nonionic surfactant are present in a weight ratio of said cationic surfactant to said hydrophilic nonionic surfactant of about 1:3.
- A composition according to any of the preceding claims which is formulated as an emulsion comprising at least two nonionic surfactants having different HLBs.
- A composition according to any of the preceding claims which further comprises a bleach activator.
- A process of bleaching fabrics, dishes or hard surfaces wherein said fabrics, dishes or hard surfaces are contacted with a bleaching liquor comprising a composition according to any of the preceding claims in an aqueous medium at a temperature of from 30°C to 90°C, and said bleaching liquor is subsequently rinsed off of said fabrics, dishes or hard surfaces.
- A process according to claim 9, wherein said fabrics are pretreated by applying thereon, preferably on the stained portions of said fabrics, a composition according to claims 1 to 8, and said pretreated fabrics are subsequently contacted with an aqueous medium at a temperature of from 30°C to 70°C, thereby forming said bleaching liquor, for a period of time sufficient to bleach said fabrics, and said bleaching liquor is subsequently rinsed off of said fabrics.
Priority Applications (9)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE1994626597 DE69426597T2 (en) | 1994-06-17 | 1994-06-17 | Bleach composition based on cationic and non-ionic surfactant mixtures |
EP19940870098 EP0687727B1 (en) | 1994-06-17 | 1994-06-17 | Bleaching compositions based on mixtures of cationic and nonionic surfactants |
ES94870098T ES2152974T3 (en) | 1994-06-17 | 1994-06-17 | WHITENING COMPOSITIONS BASED ON MIXTURES OF CATIONIC AND NON-IONIC TENSIOACTIVE. |
JP8502166A JPH10503162A (en) | 1994-06-17 | 1995-05-18 | Bleaching composition |
PCT/US1995/006224 WO1995035256A1 (en) | 1994-06-17 | 1995-05-18 | Bleaching compositions |
MX9606568A MX9606568A (en) | 1994-06-17 | 1995-05-18 | Bleaching compositions. |
CA002191572A CA2191572A1 (en) | 1994-06-17 | 1995-05-18 | Bleaching compositions |
AU25934/95A AU703720B2 (en) | 1994-06-17 | 1995-05-18 | Bleaching compositions |
GR20000402862T GR3035270T3 (en) | 1994-06-17 | 2001-01-18 | Bleaching compositions based on benzoyl peroxide and non ionic-surfactants mixture |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP19940870098 EP0687727B1 (en) | 1994-06-17 | 1994-06-17 | Bleaching compositions based on mixtures of cationic and nonionic surfactants |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0687727A1 true EP0687727A1 (en) | 1995-12-20 |
EP0687727B1 EP0687727B1 (en) | 2001-01-17 |
Family
ID=8218649
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP19940870098 Expired - Lifetime EP0687727B1 (en) | 1994-06-17 | 1994-06-17 | Bleaching compositions based on mixtures of cationic and nonionic surfactants |
Country Status (9)
Country | Link |
---|---|
EP (1) | EP0687727B1 (en) |
JP (1) | JPH10503162A (en) |
AU (1) | AU703720B2 (en) |
CA (1) | CA2191572A1 (en) |
DE (1) | DE69426597T2 (en) |
ES (1) | ES2152974T3 (en) |
GR (1) | GR3035270T3 (en) |
MX (1) | MX9606568A (en) |
WO (1) | WO1995035256A1 (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2325471A (en) * | 1997-05-24 | 1998-11-25 | Procter & Gamble | A detergent composition |
WO1999036502A1 (en) * | 1998-01-14 | 1999-07-22 | Cognis Deutschland Gmbh | Aqueous bleaching agents in the form of a microemulsion |
EP0934380A1 (en) * | 1996-10-18 | 1999-08-11 | The Procter & Gamble Company | A detergent composition |
WO2004041982A1 (en) * | 2002-11-04 | 2004-05-21 | Unilever Plc | Laundry detergent composition |
CN100549151C (en) * | 2002-11-04 | 2009-10-14 | 荷兰联合利华有限公司 | Laundry detergent composition |
WO2010109166A1 (en) * | 2009-03-25 | 2010-09-30 | Reckitt Benckiser N.V. | Composition |
WO2012120304A1 (en) * | 2011-03-09 | 2012-09-13 | Reckitt Benckiser N.V. | Carpet cleaning composition |
EP2700705A1 (en) * | 2011-04-22 | 2014-02-26 | Kao Corporation | Liquid detergent composition |
US20150282480A1 (en) * | 2014-04-08 | 2015-10-08 | Lonza, Inc. | Fast acting disinfection composition |
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EP0000226A1 (en) * | 1977-06-29 | 1979-01-10 | THE PROCTER & GAMBLE COMPANY | Laundry additive substrate for stain removal |
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GR66580B (en) * | 1978-01-11 | 1981-03-27 | Procter & Gamble | |
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EP0028432B1 (en) * | 1979-11-03 | 1984-01-18 | THE PROCTER & GAMBLE COMPANY | Granular laundry compositions |
US4399049A (en) * | 1981-04-08 | 1983-08-16 | The Procter & Gamble Company | Detergent additive compositions |
US4430236A (en) * | 1981-06-22 | 1984-02-07 | Texize, Division Of Mortonthiokol | Liquid detergent composition containing bleach |
-
1994
- 1994-06-17 DE DE1994626597 patent/DE69426597T2/en not_active Expired - Fee Related
- 1994-06-17 ES ES94870098T patent/ES2152974T3/en not_active Expired - Lifetime
- 1994-06-17 EP EP19940870098 patent/EP0687727B1/en not_active Expired - Lifetime
-
1995
- 1995-05-18 WO PCT/US1995/006224 patent/WO1995035256A1/en active Application Filing
- 1995-05-18 JP JP8502166A patent/JPH10503162A/en not_active Withdrawn
- 1995-05-18 MX MX9606568A patent/MX9606568A/en not_active IP Right Cessation
- 1995-05-18 AU AU25934/95A patent/AU703720B2/en not_active Ceased
- 1995-05-18 CA CA002191572A patent/CA2191572A1/en not_active Abandoned
-
2001
- 2001-01-18 GR GR20000402862T patent/GR3035270T3/en not_active IP Right Cessation
Patent Citations (4)
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EP0000226A1 (en) * | 1977-06-29 | 1979-01-10 | THE PROCTER & GAMBLE COMPANY | Laundry additive substrate for stain removal |
EP0004121A1 (en) * | 1978-03-13 | 1979-09-19 | THE PROCTER & GAMBLE COMPANY | Low phosphate laundry detergent compositions |
EP0012483A1 (en) * | 1978-12-15 | 1980-06-25 | THE PROCTER & GAMBLE COMPANY | Detergent compositions containing nonionic and cationic surfactants |
GB2179364A (en) * | 1985-08-20 | 1987-03-04 | Colgate Palmolive Co | Built liquid detergent compositions containing stabilizing agents |
Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0934380A1 (en) * | 1996-10-18 | 1999-08-11 | The Procter & Gamble Company | A detergent composition |
EP0934380A4 (en) * | 1996-10-18 | 1999-12-22 | Procter & Gamble | A detergent composition |
GB2325471A (en) * | 1997-05-24 | 1998-11-25 | Procter & Gamble | A detergent composition |
WO1999036502A1 (en) * | 1998-01-14 | 1999-07-22 | Cognis Deutschland Gmbh | Aqueous bleaching agents in the form of a microemulsion |
WO2004041982A1 (en) * | 2002-11-04 | 2004-05-21 | Unilever Plc | Laundry detergent composition |
US7078373B2 (en) | 2002-11-04 | 2006-07-18 | Unilever Home & Personal Care Usa Division Of Conopco, Inc. | Laundry detergent composition |
CN100549151C (en) * | 2002-11-04 | 2009-10-14 | 荷兰联合利华有限公司 | Laundry detergent composition |
US20120090100A1 (en) * | 2009-03-25 | 2012-04-19 | Reckitt Benckiser N.V. | Composition |
WO2010109166A1 (en) * | 2009-03-25 | 2010-09-30 | Reckitt Benckiser N.V. | Composition |
WO2012120304A1 (en) * | 2011-03-09 | 2012-09-13 | Reckitt Benckiser N.V. | Carpet cleaning composition |
US9382503B2 (en) | 2011-03-09 | 2016-07-05 | Reckitt Benckiser Vanish B.V. | Carpet cleaning composition |
EP2700705A1 (en) * | 2011-04-22 | 2014-02-26 | Kao Corporation | Liquid detergent composition |
EP2700705A4 (en) * | 2011-04-22 | 2014-08-27 | Kao Corp | Liquid detergent composition |
US20150282480A1 (en) * | 2014-04-08 | 2015-10-08 | Lonza, Inc. | Fast acting disinfection composition |
US10206392B2 (en) * | 2014-04-08 | 2019-02-19 | Lonza, Inc. | Fast acting disinfection composition |
US11140898B2 (en) | 2014-04-08 | 2021-10-12 | Lonza, Llc | Fast acting disinfection composition |
Also Published As
Publication number | Publication date |
---|---|
CA2191572A1 (en) | 1995-12-28 |
AU2593495A (en) | 1996-01-15 |
GR3035270T3 (en) | 2001-04-30 |
JPH10503162A (en) | 1998-03-24 |
DE69426597D1 (en) | 2001-02-22 |
MX9606568A (en) | 1997-03-29 |
EP0687727B1 (en) | 2001-01-17 |
AU703720B2 (en) | 1999-04-01 |
WO1995035256A1 (en) | 1995-12-28 |
ES2152974T3 (en) | 2001-02-16 |
DE69426597T2 (en) | 2001-08-09 |
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