WO2002068572A1 - A method for removing polymer films in the manufacture of aqueous compositions containing acrylates copolymer - Google Patents
A method for removing polymer films in the manufacture of aqueous compositions containing acrylates copolymer Download PDFInfo
- Publication number
- WO2002068572A1 WO2002068572A1 PCT/US2002/005399 US0205399W WO02068572A1 WO 2002068572 A1 WO2002068572 A1 WO 2002068572A1 US 0205399 W US0205399 W US 0205399W WO 02068572 A1 WO02068572 A1 WO 02068572A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- phosphate
- composition
- pareth
- alkyl
- acrylates copolymer
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 130
- 229920001577 copolymer Polymers 0.000 title claims abstract description 45
- 238000000034 method Methods 0.000 title claims abstract description 26
- 238000004519 manufacturing process Methods 0.000 title claims description 18
- 229920006254 polymer film Polymers 0.000 title description 4
- 229910019142 PO4 Inorganic materials 0.000 claims abstract description 68
- 239000010452 phosphate Substances 0.000 claims abstract description 68
- -1 phosphate ester Chemical class 0.000 claims abstract description 40
- 239000004094 surface-active agent Substances 0.000 claims abstract description 35
- 239000002904 solvent Substances 0.000 claims abstract description 17
- 230000001464 adherent effect Effects 0.000 claims abstract description 8
- 238000005406 washing Methods 0.000 claims abstract description 6
- 238000001704 evaporation Methods 0.000 claims abstract description 5
- 230000008020 evaporation Effects 0.000 claims abstract description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 38
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 36
- 229920000642 polymer Polymers 0.000 claims description 35
- 238000004140 cleaning Methods 0.000 claims description 26
- 125000000217 alkyl group Chemical group 0.000 claims description 22
- 229910001220 stainless steel Inorganic materials 0.000 claims description 16
- 239000010935 stainless steel Substances 0.000 claims description 16
- 239000007800 oxidant agent Substances 0.000 claims description 14
- 230000002378 acidificating effect Effects 0.000 claims description 11
- 229910052751 metal Inorganic materials 0.000 claims description 9
- 239000002184 metal Substances 0.000 claims description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- 238000003860 storage Methods 0.000 claims description 5
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 4
- 229940112262 ceteareth-2 phosphate Drugs 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000011521 glass Substances 0.000 claims description 3
- VOFRZBBLONRUHY-KVVVOXFISA-N 2-(2-hydroxyethylamino)ethanol;2-[2-[2-[(z)-octadec-9-enoxy]ethoxy]ethoxy]ethyl dihydrogen phosphate Chemical compound OCCNCCO.CCCCCCCC\C=C/CCCCCCCCOCCOCCOCCOP(O)(O)=O VOFRZBBLONRUHY-KVVVOXFISA-N 0.000 claims description 2
- GLGQRQQFWLTGES-UHFFFAOYSA-N 2-[2-[2-[2-[2-(2-decoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethanol Chemical compound CCCCCCCCCCOCCOCCOCCOCCOCCOCCO GLGQRQQFWLTGES-UHFFFAOYSA-N 0.000 claims description 2
- DKELNUBFYRNPMB-UHFFFAOYSA-N 2-decoxyethanol;phosphoric acid Chemical compound OP(O)(O)=O.CCCCCCCCCCOCCO DKELNUBFYRNPMB-UHFFFAOYSA-N 0.000 claims description 2
- 229940096584 c12-15 pareth-3 Drugs 0.000 claims description 2
- ZUVCYFMOHFTGDM-UHFFFAOYSA-N hexadecyl dihydrogen phosphate Chemical compound CCCCCCCCCCCCCCCCOP(O)(O)=O ZUVCYFMOHFTGDM-UHFFFAOYSA-N 0.000 claims description 2
- GKKMCECQQIKAHA-UHFFFAOYSA-N hexadecyl dihydrogen phosphate;2-(2-hydroxyethylamino)ethanol Chemical compound OCCNCCO.CCCCCCCCCCCCCCCCOP(O)(O)=O GKKMCECQQIKAHA-UHFFFAOYSA-N 0.000 claims description 2
- 229940046947 oleth-10 phosphate Drugs 0.000 claims description 2
- 229940095127 oleth-20 Drugs 0.000 claims description 2
- 229940093446 oleth-5 Drugs 0.000 claims description 2
- 150000005846 sugar alcohols Polymers 0.000 claims description 2
- 229910000831 Steel Inorganic materials 0.000 claims 1
- 239000012670 alkaline solution Substances 0.000 claims 1
- 239000006184 cosolvent Substances 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- 239000010959 steel Substances 0.000 claims 1
- 238000012546 transfer Methods 0.000 claims 1
- 239000000118 hair dye Substances 0.000 description 23
- 239000000243 solution Substances 0.000 description 11
- 239000002562 thickening agent Substances 0.000 description 8
- 230000003647 oxidation Effects 0.000 description 7
- 238000007254 oxidation reaction Methods 0.000 description 7
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 235000019441 ethanol Nutrition 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 150000001298 alcohols Chemical class 0.000 description 5
- 239000006185 dispersion Substances 0.000 description 5
- 239000000975 dye Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 230000001590 oxidative effect Effects 0.000 description 5
- 150000003014 phosphoric acid esters Chemical class 0.000 description 5
- 239000002243 precursor Substances 0.000 description 5
- 230000008719 thickening Effects 0.000 description 5
- 239000003093 cationic surfactant Substances 0.000 description 4
- 230000003750 conditioning effect Effects 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 238000004043 dyeing Methods 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 238000010348 incorporation Methods 0.000 description 4
- 229920001296 polysiloxane Polymers 0.000 description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 125000000129 anionic group Chemical group 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000008406 cosmetic ingredient Substances 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 150000002978 peroxides Chemical class 0.000 description 3
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 3
- 238000005201 scrubbing Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- UTXPMECBRCEYCI-UHFFFAOYSA-N 2-[2-[2-[2-(4-nonylphenoxy)ethoxy]ethoxy]ethoxy]ethanol Chemical compound CCCCCCCCCC1=CC=C(OCCOCCOCCOCCO)C=C1 UTXPMECBRCEYCI-UHFFFAOYSA-N 0.000 description 2
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 239000002535 acidifier Substances 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 150000008051 alkyl sulfates Chemical class 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 229920006318 anionic polymer Polymers 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000002537 cosmetic Substances 0.000 description 2
- 229940008099 dimethicone Drugs 0.000 description 2
- 239000004205 dimethyl polysiloxane Substances 0.000 description 2
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 2
- 239000004815 dispersion polymer Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000000543 intermediate Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- 229940116391 nonoxynol-4 Drugs 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 238000000518 rheometry Methods 0.000 description 2
- BLXVTZPGEOGTGG-UHFFFAOYSA-N 2-[2-(4-nonylphenoxy)ethoxy]ethanol Chemical compound CCCCCCCCCC1=CC=C(OCCOCCO)C=C1 BLXVTZPGEOGTGG-UHFFFAOYSA-N 0.000 description 1
- 229920002126 Acrylic acid copolymer Polymers 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229920002884 Laureth 4 Polymers 0.000 description 1
- 244000007853 Sarothamnus scoparius Species 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical class OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 125000005211 alkyl trimethyl ammonium group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- YSJGOMATDFSEED-UHFFFAOYSA-M behentrimonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCCCCCC[N+](C)(C)C YSJGOMATDFSEED-UHFFFAOYSA-M 0.000 description 1
- 229940075506 behentrimonium chloride Drugs 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 150000001767 cationic compounds Chemical class 0.000 description 1
- 229920006317 cationic polymer Polymers 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 229940073669 ceteareth 20 Drugs 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 239000004035 construction material Substances 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- SFNALCNOMXIBKG-UHFFFAOYSA-N ethylene glycol monododecyl ether Chemical compound CCCCCCCCCCCCOCCO SFNALCNOMXIBKG-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 150000002314 glycerols Chemical class 0.000 description 1
- 229940051250 hexylene glycol Drugs 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- KDNFLUWYIMPBSA-UHFFFAOYSA-N hydrogen peroxide;1,3,5-triazine-2,4,6-triamine Chemical compound OO.NC1=NC(N)=NC(N)=N1 KDNFLUWYIMPBSA-UHFFFAOYSA-N 0.000 description 1
- 229940061515 laureth-4 Drugs 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 229920003145 methacrylic acid copolymer Polymers 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 239000003791 organic solvent mixture Substances 0.000 description 1
- 238000005691 oxidative coupling reaction Methods 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical class [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229940057981 stearalkonium chloride Drugs 0.000 description 1
- SFVFIFLLYFPGHH-UHFFFAOYSA-M stearalkonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 SFVFIFLLYFPGHH-UHFFFAOYSA-M 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/22—Peroxides; Oxygen; Ozone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/55—Phosphorus compounds
- A61K8/556—Derivatives containing from 2 to 10 oxyalkylene groups
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- A61K8/8152—Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/10—Preparations for permanently dyeing the hair
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C23/00—Other surface treatment of glass not in the form of fibres or filaments
- C03C23/0075—Cleaning of glass
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/02—Emulsion paints including aerosols
- C09D5/024—Emulsion paints including aerosols characterised by the additives
- C09D5/027—Dispersing agents
-
- 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
- C11D1/34—Derivatives of acids of phosphorus
- C11D1/345—Phosphates or phosphites
-
- 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
- C11D1/78—Neutral esters of acids of phosphorus
-
- 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
- C11D3/37—Polymers
- C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3757—(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions
- C11D3/3765—(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions in 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
- 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
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/521—Esters of phosphoric acids, e.g. of H3PO4
-
- 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
- C11D2111/00—Cleaning compositions characterised by the objects to be cleaned; Cleaning compositions characterised by non-standard cleaning or washing processes
- C11D2111/10—Objects to be cleaned
- C11D2111/14—Hard surfaces
- C11D2111/16—Metals
Definitions
- This invention relates to a method to facilitate the removal of adherent polymeric films from a hard surface occasioned by the evaporation of solvent from compositions containing an acrylates copolymer, the method comprising incorporating a phosphate ester surfactant into the compositions, and washing the film from the surface to which it adheres.
- the invention relates to compositions containing an oxidizing agent; an acrylates copolymer, and one or more phosphate ester surfactants, wherein said compositions are manufactured using stainless steel equipment.
- Oxidation dye precursors are colorless compounds that undergo oxidative coupling in the presence of hydrogen peroxide to form colored molecules in the cortex of the fiber.
- Such precursors namely, primary intermediates and couplers, form the basis of cosmetic products for permanently coloring hair.
- oxidation hair dye products comprise two parts - a hair dye composition containing the dye precursors in a solvent system, and a developer composition that comprises an oxidizing agent, especially hydrogen peroxide.
- the first and second parts are mixed immediately before application to the hair, at which time the precursors are able to oxidatively couple owing to the presence of the oxidizing agent.
- the final mixture as it is applied to the hair should be a thickened liquid, preferably with a thixotropic viscosity, so that it stays put on the hair and does not run or drip during the period of application.
- Many different thickening systems have been used for this purpose.
- One class of thickening agents used for this purpose is acrylates copolymers, an anionic polymer sold, e.g., under the tradename Aculyn 33 which can be included in the acidic hydrogen peroxide developer composition.
- Acrylates copolymer is the chemical designation used for acrylic acid/methacrylic acid copolymers by the International Cosmetic Ingredient Dictionary.
- the anionic acrylates copolymer is in its acidic form and the peroxide developer composition is a thin free flowing liquid.
- the pH of the mixture is alkaline, the polymer is neutralized, and thickening is provided.
- This method of thickening oxidative hair dye product compositions i.e., the composition comprising a mixture of the first part hair dye composition and the second part developer composition, is advantageous because the individual first part hair dye composition and second part developer composition can each be highly aqueous, i.e., neither requires a high viscosity or specialized rheology. Accordingly, the resulting highly aqueous, thickened hair dye product composition is characterized by having high dyeing efficiency.
- the anionic acrylates copolymer of the present invention tends to form an adherent polymeric film on the equipment (e.g., mixing tanks, storage tanks, etc.) used in manufacturing, which is difficult to remove, requiring extensive cleanup procedures.
- the equipment e.g., mixing tanks, storage tanks, etc.
- the use of a hot alkali solution has been used with some success.
- This is a particularly vexing problem when stainless steel vessels are used for formulating, e.g., hydrogen peroxide compositions, because scrubbing such vessels can scratch the surface of the vessel, requiring that the vessel be repassivated before further use.
- Developer compositions are known that contain various surfactants, e.g., polyethoxylated alcohols and phenols, such as ceteareth-20 and nonoxynol-4, and anionic surfactants such as sulfated castor oil. Even when such surfactants are present in the anionic acrylates copolymer -containing composition, the polymers tend to form adherent polymeric films and cleaning of the manufacturing vessels is a serious problem.
- surfactants e.g., polyethoxylated alcohols and phenols, such as ceteareth-20 and nonoxynol-4
- anionic surfactants such as sulfated castor oil.
- a method is provided to facilitate the cleaning of hard surfaces, e.g., glass and metal, contacted by an anionic acrylates copolymer during the manufacture of compositions containing such polymer and onto which a polymeric film had formed.
- Film formation occurs during the manufacture of such compositions in which the anionic acrylates copolymer is incorporated when the solvent, typically water or a water-soluble organic solvent mixture, has evaporated, leaving a polymer residue that adheres to the surface.
- the solvent typically water or a water-soluble organic solvent mixture
- piping, agitators, storage tanks, pumps and other equipment commonly found in chemical manufacturing plants come into contact with the polymer while dissolved or dispersed, following which the solvent evaporates leaving a residual polymeric film.
- spills as may occur during use of the polymer-containing composition, e.g., when a polymer solution is sloppily transferred to a vessel through a manhole, result in polymeric films on exterior surfaces and on platforms, etc. This also may occur during the manufacture of the anionic acrylates copolymer itself, especially during storage of aqueous solutions or dispersions of the anionic polymer prior to sale.
- the anionic acrylates copolymer may be homopolymers or copolymers, and may be linear, nonlinear or cross-linked.
- the phosphate ester surfactant has the general structure O
- R, R 1 and R 2 may be hydrogen, an alkyl of from 1 to about 22 carbons, preferably from about 12 to 18 carbons, or an alkoxylated alkyl of from 1 to about 22 carbons, preferably from about 12 to 18 carbons, and having 1 or more, preferably from about 2 to about 25, most preferably 2 to 12, moles ethylene oxide, with the proviso that at least one of R, R and R is an alkyl or alkoxylated alkyl as previously defined but having at least 6 alkyl carbons in said alkyl or alkoxylated alkyl group.
- a method of cleaning surfaces especially metal surfaces, in particular tanks, piping, agitators, pumps, and the like, used in the manufacture, transport and storage of acrylates copolymer-containing compositions, in particular aqueous compositions, onto which said polymer has formed an adherent film, comprising incorporating a phosphate ester surfactant in said compositions, and washing the surface to substantially remove the polymeric film.
- aqueous compositions are provided in which an acrylates copolymer 1 is used as a thickening agent, the aqueous compositions further comprising a phosphoric acid ester surfactant, whereby an adherent film of the polymer occasioned by the evaporative drying of the composition onto a hard surface is more easily removed from said surface.
- suitable compositions comprise acrylates copolymer; the phosphate ester surfactant, and water.
- the presence of the phosphoric acid ester surfactant facilitates the removal of the composition from metal, most especially, stainless steel surfaces.
- the present invention is most advantageous when stainless steel is used as the material of construction for the processing equipment in facilities manufacturing acrylates copolymer-containing compositions. This is because the aggressive removal of a difficult-to-remove film of acrylates copolymer may damage the stainless steel surface of equipment, especially mixing tanks. Such damage might require repassivization of the surface. Accordingly, incorporation of the phosphate ester surfactant in acrylates
- Such benefit is important in the manufacture of any product composition containing the film forming acrylates copolymer and especially where stainless steel is employed.
- One such instance is in the manufacture of oxidative hair dye products that comprise a hair dye composition of the oxidation dye precursors and a developer composition that contains an oxidizing agent, most typically hydrogen peroxide.
- the manufacture of the developer composition may incorporate acrylates copolymer where stainless steel is the construction material of choice for hydrogen peroxide and many other oxidizing agents.
- the present invention further concerns compositions containing a film forming acrylates copolymer as a solution or dispersion in an appropriate solvent.
- the present invention is drawn to such compositions containing acrylates copolymer as a non- associative-type thickening agent for oxidation hair dye products, the copolymer being present in the developer composition of that product.
- the present invention concerns a method of cleaning hard surfaces such as glass or metal, in particular metal surfaces, and especially stainless steel surfaces, onto which has formed a polymeric film of acrylates copolymer occasioned by evaporation of the solvent in which the polymer is dissolved or dispersed.
- the incorporation of a phosphate ester surfactant during manufacture of the composition facilitates removal of the film.
- the method of the present invention concerns the cleaning of stainless steel surfaces, which can become damaged during vigorous cleaning, which would then require the surface to be repassivated.
- Acrylates copolymer which is the chemical designation used by The International Cosmetic Ingredient Dictionary and Handbook (Eighth Edition, 2000), incorporated herein by reference, is a copolymer of acrylic acid, methacrylic acid or one of their simple esters, and may be the alkali metal or ammonium salts of such copolymers.
- Illustrative of acrylates copolymers are Aculyn 33, sold by Rohm and Haas; Capigel 98 sold by Seppic; Luvimer30E sold by BASF; and Salcare SC8, sold by Allied Colloids.
- compositions of the present invention are polymer thickened, acidic developer compositions containing an oxidizing agent for use in oxidation hair dye products.
- acidic compositions of course the polymer salts would not be employed.
- the term "hair dye composition” refers to the composition containing primary intermediate and coupler oxidation dyes prior to admixture with the developer composition.
- developer composition refers to compositions containing an oxidizing agent, especially hydrogen peroxide, prior to admixture with the hair dyeing composition.
- hair dye product or “hair dye system” interchangeably refers to the combination of the hair dyeing composition and the developer composition before admixture, and may further include a conditioner product and instructions, such product or system often being provided packaged as a kit.
- the term “hair dye product composition” refers to the composition formed by mixing the hair dye composition and the developer composition.
- Acrylates copolymer used as a thickening agent in such oxidative hair dye products is incorporated in the developer composition, which has an acidic pH. At the acidic pH, the polymer is dissolved or dispersed in the solvent, while at alkaline pH the polymer thickens the composition. This occurs when the developer composition is mixed with the alkaline hair dye composition to form the hair dye product composition.
- Aculyn 33 from Rohm and Haas is preferred for this purpose. See Technical Brochure FC-310a, Aculyn Thickeners and Stabilizers For Personal Care, Rohm and Haas (May 1996) incorporated by reference.
- the second essential component of the compositions of the present invention is the phosphate ester surfactant.
- Phosphate esters suitable for incorporation into the compositions of the present invention have the formula
- the phosphate ester surfactant has the general structure
- R, R 1 and R 2 may be hydrogen, an alkyl of from 1 to about 22 carbons, preferably from about 12 to 18 carbons, or an alkoxylated alkyl of from 1 to about 22 carbons, preferably from about 12 to 18 carbons, and having 1 or more, preferably from about 2 to about 25, most preferably 2 to 12, moles ethylene oxide, with the proviso that at least one of R, R 1 and R 2 is an alkyl or alkoxylated alkyl as previously defined but having at least 6 alkyl carbons in said alkyl or alkoxylated alkyl group.
- Monoesters in which R 1 and R 2 are hydrogen and R is selected from alkyls of 10 to 18 carbons and alkoxylated fatty alcohols of 10 to 18 carbons and 2 to 12 moles ethylene oxide are preferred.
- phosphate ester surfactants mention may be made of C12-16 Pareth-6 Phosphate, C8-10 Alkyl Ethyl Phosphate, C9-15 Alkyl Phosphate, Ceteareth-2 Phosphate, Ceteareth-4 Phosphate, Ceteareth-5 Phosphate, Ceteareth-10 Phosphate, Ceteth-8 Phosphate, Ceteth-10 Phosphate, Cetyl Phosphate, C6-10 Pareth-4 Phosphate, C12-13 Pareth-10 Phosphate, C12-15 Pareth-2 Phosphate, C12-15 Pareth-3 Phosphate, C12-15 Pareth-6 Phosphate, C12-15
- compositions of the present invention are aqueous, and may comprise water as the sole solvent, or may comprise water in combination with an essentially water- soluble organic solvent such as a mono- or polyhydric alcohol.
- the compositions contain a sufficient amount of solvent so that the polymer is dissolved in the composition, or is dispersed in the composition.
- water is the major component of the solvent system.
- the solvent constitutes from about 60 to about 93% of the composition on a weight basis, most preferably from about 70 to about 85 % by weight.
- Useful organic solvents are Ci to C 6 alcohols and C 2 to C 8 polyols.
- Especially useful alcohols for use in the solvent system of the present invention are ethyl alcohol, isopropyl alcohol and butyl alcohol.
- Especially useful pohydric alcohols of the present invention are ethylene glycol, propylene glycol, hexylene glycol, and glycerin.
- the alcohols typically comprise from about 0 to about 25% by weight of the composition.
- compositions of the present invention contain hydrogen peroxide and are used as developer compositions in oxidative hair dye products.
- the developer compositions comprise on a weight basis by weight of the composition: (a) from about 0.1 to about 10 of acrylates copolymer, preferably 0.2 to
- the developer composition containing the hydrogen peroxide oxidizing agent In the manufacture of the developer composition containing the hydrogen peroxide oxidizing agent, it is necessary to use stainless steel equipment, in particular stainless steel mixing tanks, to avoid corrosion caused by the hydrogen peroxide. Moreover, there is a tendency for the developer composition, which has an acidic pH, typically a pH from about 2.5 to about 6.5, to foam during mixing, mixing being necessary to ensure homogeneity of the composition. As a consequence the side wall of the tank is coated with a thin layer of developer composition, which dries rapidly when mixing ends. The resulting polymeric film has proven to be quite difficult to remove and requires exposure to high pressure cleaning sprays, often with highly alkaline cleaning products. Such treatment can cause damage to the stainless steel surface of the mixing tank, requiring it to be repassivated.
- an acidic pH typically a pH from about 2.5 to about 6.5
- developer compositions typically contain a nonionic surfactant such as nonoxynol-2, nonoxynol-4, C ⁇ -C ⁇ 5 Pareth- 7, C 12 -C 15 Pareth-9, and C12-C15 Pareth-3.
- a nonionic surfactant such as nonoxynol-2, nonoxynol-4, C ⁇ -C ⁇ 5 Pareth- 7, C 12 -C 15 Pareth-9, and C12-C15 Pareth-3.
- the incorporation of the phosphoric acid ester into the developer composition has been found effective to reduce the tenacity of the polymeric film to the side wall of the stainless steel.
- the developer compositions contain any suitable oxidizing agent, particularly hydrogen peroxide and its addition compounds.
- suitable oxidizing agents include urea peroxide, the alkali metal and ammonium salts of persulfate, perborate and percarbamate, especially the sodium salt, and melamine peroxide.
- the oxidizing agent is preferably present as a 3 to 12% (10 to 40 volume), most especially 6%, aqueous hydrogen peroxide solution. See e.g., deNavarre, The Chemistry and Manufacture of Cosmetics, Vol. IV, p.847-50, (2 nd Edition, 1975).
- the developer composition of the present invention may also contain, in addition to the anionic acrylates copolymer, hydrogen peroxide, the phosphate ester surfactant, and water, one or more additional ingredients.
- the developer composition may contain an acidifying agent to provide an acid pH, preferably in the range of from about 3 to about 5.5, most preferably from about 3.5 to about 4.5. At this pH the developer composition preferably has an essentially Newtonian rheology, with a viscosity less than about 1000 cps, preferably less than about 500 cps, most preferably less than 100 cps.
- the preferred polymer thickening agent is Aculyn 33, a copolymer of two or more monomers of acrylic acid, methacrylic acid or one of their simple esters sold by Rohm and Haas. Neutralization by raising pH converts this polymeric thickener into a clear viscous solutions.
- Such thickening occurs when the developer is admixed with the alkaline hair dye composition to provide a hair dye product composition having a pH of from about 8 to about 11 , preferably from about 9 to 10.5.
- the Aculyn 33 polymer is peroxide stable. Most preferably a mixture of an associative and non-associative polymer is employed. See U.S. Patent No. 5,376,146.
- the developer composition may also include a surfactant other than the phosphate ester surfactant, which surfactant is selected from the group consisting of anionic, nonionic, and amphoteric (including zwitterionic) surfactants.
- a surfactant other than the phosphate ester surfactant which surfactant is selected from the group consisting of anionic, nonionic, and amphoteric (including zwitterionic) surfactants.
- surfactant means a surfactant other than a cationic surfactant or a phosphate ester surfactant.
- Suitable surfactants include fatty alcohol sulfates, ethoxylated fatty alcohol sulfates, alkylsulfonates, alkylbenzensulfonates, alkyltrimethylammonium salts, alkylbetaines, ethoxylated fatty alcohols, ethoxylated fatty acids, ethoxylated alkylphenols, block polymers of ethylene and/or propylene glycol, glycerol esters, phosphate esters, fatty acid alkanol amides and ethoxylated fatty acid esters, alkyl sulfates, ethoxylated alkyl sulfates, alkyl glyceryl ether sulfonates, methyl acyl taurates, acyl isethionates, alkyl ethoxy carboxylates
- the amount of surfactants in the developer compositions is normally from about
- the developer composition may also include a conditioning agent.
- Conditioning agents include silicones and silicone derivatives; hydrocarbon oils; cationic surfactants that are monomeric quaternary compounds, and quatemized polymers.
- Monomeric quaternary compounds are typically cationic compounds, but may also include betaines and other amphoteric and zwitterionic materials that provide a conditioning effect.
- Suitable monomeric quaternary compounds include behentrimonium chloride, stearalkonium chloride, and many other compounds. See WO 98/27941 incorporated by reference.
- Quatemized polymers are typically cationic polymers, but may also include amphoteric and zwitterionic polymers.
- Useful polymers are exemplified by polyquaternium-4, polyquaternium-6, polyquatemium-7, polyquaternium-8, polyquaternium-9, polyquaternium-10, polyquaternium-22, polyquaternium-32, polyquatemium-39, polyquaternium-44 and polyquatemium-47.
- Silicones suitable to condition hair are dimethicone, amodimethicone, dimethicone copolyol and dimethiconol. See also WO 99/34770 published July 15,1999, incorporated by reference, for suitable silicones.
- Suitable hydrocarbon oils would include mineral oil.
- Conditioners are usually present in the hair developer composition in an amount of from about 0.01 to about 5% by weight of the hair dye composition.
- chelating and sequestering agents such as EDTA, dispersing agents, penetrating agents, etc., in concentrations effective to achieve their functional purpose.
- cleaning composition may include water as a medium to rinse the surface, but preferably is an aqueous solution of a cleaning active.
- Cleaning actives may include alkali materials such as sodium hydroxide, potassium hydroxide, ammonium hydroxide, (not preferred because of odor), mono-, di- and triethanolamines; anionic, nonionic and amphoteric surfactants, including the phosphate ester of the present invention, and compatible mixtures thereof.
- the pH of the cleaning composition will be alkaline or neutral, most especially alkaline with a pH of from about 8 to about 10.
- a particularly useful cleaner is DuBois T-Off, a commercially available caustic-containing cleaner, in a 5 to 15%, preferably 10% aqueous solution.
- the DuBois T-Off solution preferably is used at elevated temperature, especially from about 45 to 65°C.
- the cleaning composition is sprayed under a moderate pressure of from about 15 to about 65 psig, most preferably from about 20 to about 40 psig, until the film is removed.
- the cleaning time varies depending upon the nature of the cleaning solution, the temperature of cleaning, the time between cleanings, and the age of the film. Generally, the wash time is from one to several minutes to two hours in the case of a long-term film build-up.
- the film is removed substantially, e.g., 90%» or more of the film, in less than one hour.
- the application of the cleaning composition may be accompanied by scrubbing with a broom, brush or other device. Scrubbing is not preferred where the surface being cleaned is stainless steel.
- Examples of two developer compositions containing 6.15% hydrogen peroxide (approximately 20 volume H 2 O 2 ); an anionic acrylates copolymer thickening agent, sufficient acidifying agent to provide a pH of 2.5-5, and varying concentrations of the phosphate ester surfactant laureth-4 phosphate are set forth in Table 1 below.
- Aculyn 22 is a 30% active polymer dispersion, and Aculyn is a 28% active polymer dispersion.
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Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
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DE60238972T DE60238972D1 (en) | 2001-02-27 | 2002-02-22 | METHOD OF REMOVING POLYMERIC FILMS IN THE PREPARATION OF ACRYLATE COPOLYMER-CONTAINING AQUEOUS COMPOSITIONS |
JP2002568669A JP2005506395A (en) | 2001-02-27 | 2002-02-22 | Method for removing a polymer coating in the manufacture of an aqueous composition containing an acrylate copolymer |
AT02723221T ATE495727T1 (en) | 2001-02-27 | 2002-02-22 | METHOD FOR REMOVAL OF POLYMER FILM IN THE PRODUCTION OF AQUEOUS COMPOSITIONS CONTAINING ACRYLIC COPOLYMER |
EP02723221A EP1373447B1 (en) | 2001-02-27 | 2002-02-22 | A method for removing polymer films in the manufacture of aqueous compositions containing acrylates copolymer |
MXPA03007726A MXPA03007726A (en) | 2001-02-27 | 2002-02-22 | A method for removing polymer films in the manufacture of aqueous compositions containing acrylates copolymer. |
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US27181201P | 2001-02-27 | 2001-02-27 | |
US60/271,812 | 2001-02-27 |
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PCT/US2002/005398 WO2002068488A2 (en) | 2001-02-27 | 2002-02-22 | A method for removing polymer films in the manufacture of aqueous compositions containing anionic amphiphilic polymers |
PCT/US2002/005399 WO2002068572A1 (en) | 2001-02-27 | 2002-02-22 | A method for removing polymer films in the manufacture of aqueous compositions containing acrylates copolymer |
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PCT/US2002/005398 WO2002068488A2 (en) | 2001-02-27 | 2002-02-22 | A method for removing polymer films in the manufacture of aqueous compositions containing anionic amphiphilic polymers |
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US (2) | US6984268B2 (en) |
EP (2) | EP1373447B1 (en) |
JP (2) | JP2005506395A (en) |
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AT (2) | ATE495795T1 (en) |
AU (1) | AU2002254013A1 (en) |
DE (2) | DE60238972D1 (en) |
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WO (2) | WO2002068488A2 (en) |
Cited By (1)
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CN115635264A (en) * | 2022-12-26 | 2023-01-24 | 怡隆(廊坊)环保科技发展有限公司 | Machined part polishing forming device and production flow thereof |
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US20060134049A1 (en) * | 2004-12-17 | 2006-06-22 | Keenan Andrea C | Hair styling compositions |
CA2651186C (en) * | 2006-05-08 | 2013-07-02 | Ecolab Inc. | Acidic cleaner for metal surfaces |
US20100260696A1 (en) * | 2007-08-02 | 2010-10-14 | Clariant Finance (Bvi) Limited | Aqueous Compositions Containing Alkoxylated Phosphoric Acid Triesters |
EP2387988B1 (en) | 2010-05-19 | 2017-09-27 | The Procter & Gamble Company | Oxidizing composition for the treatment of keratin fibres |
WO2013029859A1 (en) * | 2011-08-26 | 2013-03-07 | Henkel Ag & Co. Kgaa | Agent comprising hydrogen peroxide having improved viscosity adjustment |
US9863062B2 (en) | 2013-03-14 | 2018-01-09 | Corner Star Limited | Czochralski crucible for controlling oxygen and related methods |
CN103344639B (en) * | 2013-07-11 | 2015-10-28 | 山东大学 | The detector tube of pyrroles's adduct in a kind of quick detection urine |
CN108938458A (en) * | 2018-09-30 | 2018-12-07 | 浙江大学华南工业技术研究院 | A kind of acidic hair coloring preparation composition |
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2002
- 2002-02-22 WO PCT/US2002/005398 patent/WO2002068488A2/en active Application Filing
- 2002-02-22 MX MXPA03007726A patent/MXPA03007726A/en active IP Right Grant
- 2002-02-22 US US10/080,458 patent/US6984268B2/en not_active Expired - Fee Related
- 2002-02-22 JP JP2002568669A patent/JP2005506395A/en active Pending
- 2002-02-22 EP EP02723221A patent/EP1373447B1/en not_active Expired - Lifetime
- 2002-02-22 CN CNB028050215A patent/CN1228428C/en not_active Expired - Fee Related
- 2002-02-22 DE DE60238972T patent/DE60238972D1/en not_active Expired - Lifetime
- 2002-02-22 EP EP02723220A patent/EP1383859B1/en not_active Expired - Lifetime
- 2002-02-22 DE DE60238975T patent/DE60238975D1/en not_active Expired - Lifetime
- 2002-02-22 AT AT02723220T patent/ATE495795T1/en not_active IP Right Cessation
- 2002-02-22 AU AU2002254013A patent/AU2002254013A1/en not_active Abandoned
- 2002-02-22 JP JP2002567997A patent/JP2004527604A/en active Pending
- 2002-02-22 US US10/080,459 patent/US6936113B2/en not_active Expired - Lifetime
- 2002-02-22 CN CNB028050681A patent/CN1260338C/en not_active Expired - Fee Related
- 2002-02-22 AT AT02723221T patent/ATE495727T1/en not_active IP Right Cessation
- 2002-02-22 WO PCT/US2002/005399 patent/WO2002068572A1/en active Application Filing
- 2002-02-22 MX MXPA03007725A patent/MXPA03007725A/en active IP Right Grant
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US6936113B2 (en) | 2005-08-30 |
ATE495795T1 (en) | 2011-02-15 |
US6984268B2 (en) | 2006-01-10 |
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JP2004527604A (en) | 2004-09-09 |
WO2002068488A2 (en) | 2002-09-06 |
EP1373447B1 (en) | 2011-01-19 |
MXPA03007725A (en) | 2003-12-04 |
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CN1228428C (en) | 2005-11-23 |
DE60238972D1 (en) | 2011-03-03 |
MXPA03007726A (en) | 2003-12-04 |
CN1491274A (en) | 2004-04-21 |
EP1373447A1 (en) | 2004-01-02 |
CN1260338C (en) | 2006-06-21 |
US20020183221A1 (en) | 2002-12-05 |
EP1383859A2 (en) | 2004-01-28 |
EP1373447A4 (en) | 2010-02-24 |
ATE495727T1 (en) | 2011-02-15 |
EP1383859B1 (en) | 2011-01-19 |
EP1383859A4 (en) | 2010-02-24 |
US20020160923A1 (en) | 2002-10-31 |
WO2002068488A3 (en) | 2003-05-01 |
AU2002254013A1 (en) | 2002-09-12 |
JP2005506395A (en) | 2005-03-03 |
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