MXPA06014932A - Photo bleach compositions. - Google Patents
Photo bleach compositions.Info
- Publication number
- MXPA06014932A MXPA06014932A MXPA06014932A MXPA06014932A MXPA06014932A MX PA06014932 A MXPA06014932 A MX PA06014932A MX PA06014932 A MXPA06014932 A MX PA06014932A MX PA06014932 A MXPA06014932 A MX PA06014932A MX PA06014932 A MXPA06014932 A MX PA06014932A
- Authority
- MX
- Mexico
- Prior art keywords
- ppm
- photobleaching
- composition
- extender
- water
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 108
- 239000007844 bleaching agent Substances 0.000 title description 19
- 239000003504 photosensitizing agent Substances 0.000 claims abstract description 45
- 238000004061 bleaching Methods 0.000 claims abstract description 22
- 238000004140 cleaning Methods 0.000 claims abstract description 19
- 238000000034 method Methods 0.000 claims abstract description 13
- 239000007788 liquid Substances 0.000 claims description 26
- 239000004606 Fillers/Extenders Substances 0.000 claims description 21
- 239000004615 ingredient Substances 0.000 claims description 21
- 238000005406 washing Methods 0.000 claims description 21
- 239000004744 fabric Substances 0.000 claims description 19
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 16
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 15
- 229910052760 oxygen Inorganic materials 0.000 claims description 14
- 239000001301 oxygen Substances 0.000 claims description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- -1 phthalocyanines Chemical group 0.000 claims description 11
- 239000000463 material Substances 0.000 claims description 10
- 239000004094 surface-active agent Substances 0.000 claims description 10
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 claims description 7
- SMNDYUVBFMFKNZ-UHFFFAOYSA-N 2-furoic acid Chemical compound OC(=O)C1=CC=CO1 SMNDYUVBFMFKNZ-UHFFFAOYSA-N 0.000 claims description 6
- 125000000217 alkyl group Chemical class 0.000 claims description 6
- GSNUFIFRDBKVIE-UHFFFAOYSA-N 2,5-dimethylfuran Chemical compound CC1=CC=C(C)O1 GSNUFIFRDBKVIE-UHFFFAOYSA-N 0.000 claims description 4
- IHCCAYCGZOLTEU-UHFFFAOYSA-N 3-furoic acid Chemical compound OC(=O)C=1C=COC=1 IHCCAYCGZOLTEU-UHFFFAOYSA-N 0.000 claims description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical group C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 4
- 229910052710 silicon Inorganic materials 0.000 claims description 4
- 230000002087 whitening effect Effects 0.000 claims description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 3
- OUUQCZGPVNCOIJ-UHFFFAOYSA-M Superoxide Chemical compound [O-][O] OUUQCZGPVNCOIJ-UHFFFAOYSA-M 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 150000003233 pyrroles Chemical class 0.000 claims description 3
- 239000010703 silicon Substances 0.000 claims description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical group [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 2
- HUVXQFBFIFIDDU-UHFFFAOYSA-N aluminum phthalocyanine Chemical class [Al+3].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 HUVXQFBFIFIDDU-UHFFFAOYSA-N 0.000 claims description 2
- 150000002240 furans Chemical class 0.000 claims description 2
- 150000002460 imidazoles Chemical class 0.000 claims description 2
- 150000004032 porphyrins Chemical group 0.000 claims description 2
- DLOBKMWCBFOUHP-UHFFFAOYSA-N pyrene-1-sulfonic acid Chemical compound C1=C2C(S(=O)(=O)O)=CC=C(C=C3)C2=C2C3=CC=CC2=C1 DLOBKMWCBFOUHP-UHFFFAOYSA-N 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- 239000012530 fluid Substances 0.000 abstract 2
- 238000009897 hydrogen peroxide bleaching Methods 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 23
- 241000894007 species Species 0.000 description 10
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- 239000000975 dye Substances 0.000 description 9
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- 102000004190 Enzymes Human genes 0.000 description 7
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- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
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- 238000012546 transfer Methods 0.000 description 5
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- OFFSPAZVIVZPHU-UHFFFAOYSA-N 1-benzofuran-2-carboxylic acid Chemical compound C1=CC=C2OC(C(=O)O)=CC2=C1 OFFSPAZVIVZPHU-UHFFFAOYSA-N 0.000 description 4
- CBEFMGJHEKAMNI-UHFFFAOYSA-N 9-oxofluorene-1-carboxylic acid Chemical compound C12=CC=CC=C2C(=O)C2=C1C=CC=C2C(=O)O CBEFMGJHEKAMNI-UHFFFAOYSA-N 0.000 description 4
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
- OOGYVVYCCYJADG-UHFFFAOYSA-N acridine-1-carboxylic acid Chemical compound C1=CC=C2C=C3C(C(=O)O)=CC=CC3=NC2=C1 OOGYVVYCCYJADG-UHFFFAOYSA-N 0.000 description 4
- 239000012190 activator Substances 0.000 description 4
- 125000002091 cationic group Chemical group 0.000 description 4
- 239000002738 chelating agent Substances 0.000 description 4
- 239000002270 dispersing agent Substances 0.000 description 4
- 230000002401 inhibitory effect Effects 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
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- 125000000129 anionic group Chemical group 0.000 description 3
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- XPFVYQJUAUNWIW-UHFFFAOYSA-N furfuryl alcohol Chemical compound OCC1=CC=CO1 XPFVYQJUAUNWIW-UHFFFAOYSA-N 0.000 description 3
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- 239000000126 substance Substances 0.000 description 3
- CIOXZGOUEYHNBF-UHFFFAOYSA-N (carboxymethoxy)succinic acid Chemical compound OC(=O)COC(C(O)=O)CC(O)=O CIOXZGOUEYHNBF-UHFFFAOYSA-N 0.000 description 2
- APQSQLNWAIULLK-UHFFFAOYSA-N 1,4-dimethylnaphthalene Chemical compound C1=CC=C2C(C)=CC=C(C)C2=C1 APQSQLNWAIULLK-UHFFFAOYSA-N 0.000 description 2
- FAGGUIDTQQXDSJ-UHFFFAOYSA-N 3-benzoylazepan-2-one Chemical compound C=1C=CC=CC=1C(=O)C1CCCCNC1=O FAGGUIDTQQXDSJ-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 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 2
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 2
- 108090000854 Oxidoreductases Proteins 0.000 description 2
- 102000004316 Oxidoreductases Human genes 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical class C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- AUNGANRZJHBGPY-SCRDCRAPSA-N Riboflavin Chemical compound OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-SCRDCRAPSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- BGRWYDHXPHLNKA-UHFFFAOYSA-N Tetraacetylethylenediamine Chemical compound CC(=O)N(C(C)=O)CCN(C(C)=O)C(C)=O BGRWYDHXPHLNKA-UHFFFAOYSA-N 0.000 description 2
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- VFLDPWHFBUODDF-FCXRPNKRSA-N curcumin Chemical compound C1=C(O)C(OC)=CC(\C=C\C(=O)CC(=O)\C=C\C=2C=C(OC)C(O)=CC=2)=C1 VFLDPWHFBUODDF-FCXRPNKRSA-N 0.000 description 2
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- 239000012535 impurity Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229920000831 ionic polymer Polymers 0.000 description 1
- 108010059345 keratinase Proteins 0.000 description 1
- 229910052745 lead Inorganic materials 0.000 description 1
- 108010062085 ligninase Proteins 0.000 description 1
- 235000019421 lipase Nutrition 0.000 description 1
- 229910001425 magnesium ion Inorganic materials 0.000 description 1
- 150000002697 manganese compounds Chemical class 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- CXKWCBBOMKCUKX-UHFFFAOYSA-M methylene blue Chemical compound [Cl-].C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 CXKWCBBOMKCUKX-UHFFFAOYSA-M 0.000 description 1
- 229960000907 methylthioninium chloride Drugs 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 239000002324 mouth wash Substances 0.000 description 1
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 1
- 229910052755 nonmetal Inorganic materials 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 150000004965 peroxy acids Chemical class 0.000 description 1
- FVDOBFPYBSDRKH-UHFFFAOYSA-N perylene-3,4,9,10-tetracarboxylic acid Chemical compound C=12C3=CC=C(C(O)=O)C2=C(C(O)=O)C=CC=1C1=CC=C(C(O)=O)C2=C1C3=CC=C2C(=O)O FVDOBFPYBSDRKH-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920002006 poly(N-vinylimidazole) polymer Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920001444 polymaleic acid Polymers 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- 239000002151 riboflavin Substances 0.000 description 1
- 235000019192 riboflavin Nutrition 0.000 description 1
- 229960002477 riboflavin Drugs 0.000 description 1
- 229930187593 rose bengal Natural products 0.000 description 1
- 229940081623 rose bengal Drugs 0.000 description 1
- STRXNPAVPKGJQR-UHFFFAOYSA-N rose bengal A Natural products O1C(=O)C(C(=CC=C2Cl)Cl)=C2C21C1=CC(I)=C(O)C(I)=C1OC1=C(I)C(O)=C(I)C=C21 STRXNPAVPKGJQR-UHFFFAOYSA-N 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
- PZGANULLXCGPFZ-UHFFFAOYSA-N zinc;5,10,15,20-tetrapyridin-4-ylporphyrin-22,24-diide Chemical compound [Zn+2].C1=CC(C(=C2C=CC([N-]2)=C(C=2C=CN=CC=2)C=2C=CC(N=2)=C(C=2C=CN=CC=2)C2=CC=C3[N-]2)C=2C=CN=CC=2)=NC1=C3C1=CC=NC=C1 PZGANULLXCGPFZ-UHFFFAOYSA-N 0.000 description 1
- 239000002888 zwitterionic surfactant Substances 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/40—Dyes ; Pigments
-
- 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
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0063—Photo- activating 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
- C11D3/40—Dyes ; Pigments
- C11D3/42—Brightening agents ; Blueing agents
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
- D06L4/00—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
- D06L4/10—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which develop oxygen
- D06L4/12—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which develop oxygen combined with specific additives
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
- D06L4/00—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
- D06L4/50—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs by irradiation or ozonisation
-
- 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
- C11D2111/12—Soft surfaces, e.g. textile
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Textile Engineering (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Detergent Compositions (AREA)
Abstract
The present invention relates to compositions comprising a photosensitizer that can be used to provide aqueous fluids with bleaching capabilities, aqueous fluid photobleaching compositions having bleaching capabilities and processes of making and using same. Such compositions can provide bleaching and/or cleaning benefits that are similar to or better than hydrogen peroxide bleaching systems.
Description
PHOTOBLANKING COMPOSITIONS
FIELD OF THE INVENTION
The present invention relates to photobleaching compositions having bleaching capabilities, and processes for manufacturing and using the same.
BACKGROUND OF THE INVENTION
Conventional bleaching compositions usually employ hydrogen peroxide as a bleaching species or as an intermediate ingredient that is converted to a peracid. These systems can provide effective whitening. Unfortunately it is difficult to formulate stable versions of these systems that are also not volume efficient since the required bleaching components make up a considerable volume of any formulation. Although photo-bleach systems do not suffer from the formulation and volume problems of hydrogen peroxide systems, photo-bleach systems tend to be less effective since the short life of the bleaching species requires that the photosensitizer, oxygen, and light be present simultaneously in the place. In addition, the selection of effective photo-bleaches used in traditional photo-bleach systems is limited since photobleaches generally must be capable of being adsorbed on the dirty portion of the site. As a consequence, the photobleaching systems would be attractive if the life of the bleaching species could be extended to allow the diffusion of said species in the washing solution.
BRIEF DESCRIPTION OF THE INVENTION
The present invention relates to photobleaching compositions comprising a photosensitizer which can be used to provide an aqueous liquid with bleaching capabilities, aqueous liquid cleaning compositions having photobleaching capabilities and processes for manufacturing and using the same. These and other aspects, features and advantages will be evident to those who have experience in the industry from reading the following detailed description and the appended claims.
DETAILED DESCRIPTION OF THE INVENTION
Definitions The term "photobleaching composition", as used herein and unless otherwise indicated, includes multipurpose or "high performance" cleaning agents in granular or powdered form; liquid, gel or multi-purpose paste cleaning agents, especially so-called high-performance liquids; liquid detergents for fine fabrics; agents for the manual washing of dishes, or agents of low performance for the washing of crockery, especially those of great volume of foam; agents for dishwashing, including the various types of tablets, granules, adjuvants and rinsing liquids, for domestic and institutional use; liquid disinfecting and cleaning agents, including those of the antibacterial type for washing hands, cleaning sticks, mouth rinses, denture cleaners, shampoos for carpets or trolleys, cleaners for bathrooms; shampoos and hair rinses; gels for shower and bath foams and metal cleaners; as well as cleaning aids such as bleach additives and "bar stain cleaners" or pretreatment type. The term "fabrics" and "cloth", as used herein, comprises articles of clothing, linens, curtains, and accessories for garments. The term also covers other articles made totally or partially with fabric, for example, bags, furniture covers, tarpaulins and the like. The term "dirt" means any unwanted substance in a fabric. The terms "water-based" or "hydrophilic" dirt refer to the dirt containing water at the time it came into contact with the cloth article or to the dirt retaining a significant portion of water in the cloth article. Examples of water-based soiling include, but are not limited to: beverages, dirt from many foods, water soluble dyes, body fluids, such as sweat, urine or blood, and dirt from outdoor spaces, such as grass and mud stains. The term "aqueous liquid", as used herein, means any liquid or mixture of liquids comprising more than 5%, more than 25%, more than 50% or alternatively more than 90% water. The term "soluble", as used herein, is used to describe one or more "photosensitizing" media capable of forming a solution at a concentration of at least 1 x 10"8 molar in water at a pH of use of 10 to 8. As used herein, articles a and a when used in a claim, for example, "an emulsifier" or "a photosensitizer" is understood to mean one or more of the material claimed or described, unless otherwise specified, all levels of the component or composition are expressed in reference to the active level of that component or composition, and are exclusive of impurities, for example, residual solvents or by-products; which may be present in commercially available sources All percentages and proportions are calculated by weight, unless otherwise indicated.All percentages and proportions are calculated based on the total composition, unless otherwise specified.
All temperatures are in degrees Celsius (° C) unless otherwise specified. All measurements are given in international standard units unless otherwise specified. It will be understood that each maximum numerical limitation given in this specification will include any lower numerical limitation, as if the lower numerical limitations had been explicitly annotated herein. Any minimum numerical limit cited in this specification shall include any major numerical limit as if such major numerical limits had been explicitly quoted herein. Any numerical range quoted in this specification shall include any minor interval that falls within the larger numerical range as if all minor numerical intervals had been explicitly quoted herein. All documents cited herein are considered incorporated in their relevant part as reference. The mention of any document should not be construed as an admission that it corresponds to a prior industry with respect to the present invention.
Photobleaching Compositions Applicants have discovered that certain photosensitizing compositions are unexpectedly suitable for incorporation in aqueous liquids. Suitable photosensitizing compositions usually contain a photosensitizer and an extender, and may contain optional ingredients such as anionic, cationic, nonionic, and zwitterionic surfactants. The solid compositions, based on the total weight of said composition, may comprise from about 0.1% to about 50%, from about 1% to about 25%, or even from about 5% to about 20% of a photosensitizer; from about 1% to about 99.9%, from about 5% to about 90%, or even from about 10% to about 50% of an extender, the balance of said compositions being an optional / additional ingredient. These solid compositions include, but are not limited to, powders and granules. The liquid photosensitizing compositions may comprise, based on the total weight of said composition, from about 0.1% to about 50%, from about 1% to about 25%, or even from about 5% to about 20% of a photosensitizer; from about 1% to about 99.9%, from about 5% to about 90%, or even from about 10% to about 50% of an extender, the balance of said photobleaching compositions being an aqueous liquid or a mixture of an aqueous liquid and an optional / additional ingredient. The solid photosensitizing compositions and liquid photosensitizer compositions mentioned above can be packaged in a kit containing instructions for use. Unlike common photobleaching compositions, the aforementioned compositions do not require that the photosensitizer, oxygen, light and place are present simultaneously since it is considered that the whitening species is formed in solution and also, due to the use of an extender, this species has enough life to spread to the dirty portion of the place. In addition, the use of an extender increases the selection of photosensitizers for the formulator, since these photosensitizers do not require that they be capable of being adsorbed on the dirty portion of the site.
Production process Without theoretical limitations of any kind, the applicants consider that the formation and concentration of whitening species other than atomic oxygen are a function of at least 4 variables: concentration of the reactant, time, oxygen concentration of the reactant mixture , and photon flow. As a consequence, although applicants consider that photobleaching compositions can be made by combining a photosensitizer and an extender, any aqueous liquid solvent and any optional ingredient, the light energy obtained from light having a wavelength that can be absorbed by the photosensitizer and / or the amount of oxygen in the composition or to a minimum is reduced to a minimum. the one that exposes the composition. For the purposes of the present invention, the wavelength of the light that any photosensitizer will absorb is determined by means of the Light Absorbance Test detailed in the Test Methods section of this specification. For the purposes of the present invention, the minimization of the light energy that the photosensitizer can absorb means that during processing those compositions are generally exposed to that wavelength of light at one of the following levels: less than about 1 milliwatt per meter square of solution surface exposed to that light, less than about 1x 10"4 watts per square meter of solution surface exposed to that light, or even less than about 1 microwatt per square meter of solution surface exposed to that light. For purposes of the present invention, oxygen minimization refers to that during processing, the compositions comprise less than about 1 x 10"2 moles of oxygen per liter, less than about 1 x 103 moles of oxygen per liter, and even less than about 1 x 10 ~ 4 moles of oxygen per liter. In use the photobleaching compositions can be made by exposing the photobleaching compositions described herein to light having a wavelength that can be absorbed by that of the photosensitizer and sufficient oxygen to provide said composition with a dissolved oxygen content greater than about 1 x. 10'9 moles per liter, greater than about 1 x 10"6 moles per liter, or even greater than about 1 x 10" 3 moles per liter. Generally, the amount of that light energy needed to produce those compositions in use is greater than about 1 x 10 ^ milliwatts per square meter of solution surface exposed to that light, greater than about 1 milliwatt per square meter of solution surface exposed to that light, or even greater than 1 x 10"2 watts / square meter of solution surface exposed to that light, said light energy can be provided by any suitable source, including but not limited to a light source located in a appliance, said household appliance is suitable for cleaning and / or fabrics.
Method of use A place, including a surface or a fabric, can be bleached by contacting at least a portion of said place with a liquid version of the photobleaching compositions of the applicants, further characterized in that the extensor and the photosensitizer are dissolved in a liquid watery or dissolve while in contact with the place. These compositions can be in pure form or diluted in a washing solution. As the experienced technician will appreciate, contact includes but is not limited to immersion and spraying. After this step of contacting, the place can optionally be washed and / or rinsed. This composition in use can be made during the time they are in contact with the article or articles to be washed.
Suitable materials Suitable materials for making the photobleaching compositions of the applicants include any photosensitizer or mixture of photosensitizers that generate singlet oxygen and that are soluble in an aqueous liquid. Suitable singlet oxygen photosensitizers include the water-soluble porphyrins and phthalocyanines and their complexes with a photoactive metal / non-metal selected from Sn, Ge, Pt, Pd, Pb, Si, Zn, Al. For example, sulfonated zinc phthalocyanine, sulfonated aluminum phthalocyanine, silicon phthalocyanine-di-isoPEG 384 and other water soluble phthalocyanines described in U.S. Pat. no. 5,916,481, zinc-5,10,15,20-tetra (4-pyridyl) -21 H, 23H-porphine tetrakis (methochloride), tetrakis of benzoic acid, sodium salt. Other suitable photosensitizers include aromatic singlet oxygen photosensitizers and water-soluble heteroaromatics, such as acridinecarboxylic acid, perylene-tetracarboxylic acid, pyrenesulfonic acid, 9-fluorenone-1-carboxylic acid. Other photosensitizers soluble in water are methylene blue, rose bengal, riboflavin. Examples of superoxide photosensitizers include the substituted triethanolamine silicon phthalocyanines described in U.S. Pat. no. 6,225,273 and curcumin. Suitable water-soluble photosensitizers can be obtained from Sigma-Aldrich of ilwaukee, Wisconsin U.S. A. Ciba Specialty Chemicals Inc. of Basel, Switzerland or can be prepared by the procedures described in the literature. Suitable extenders include species that form adducts with singlet oxygen or superoxide. For example, suitable atomic oxygen extenders include extenders selected from the group comprising furan, substituted furans, polyethoxylates, alkyl polyethoxylates, polynuclear aromatics, imidazole, substituted imidazoles, pyrrole, substituted pyrroles, and mixtures thereof. Examples of suitable extenders include: furfuryl alcohol, 2-furoic acid, 3-furoic acid, 3-furanmethanol, 2-benzofurancarboxylic acid, 1,4-dimethylnaphthalene, furfural, 2,5-dimethyl furan and mixtures thereof. These materials can be obtained from Sigma-Aldrich of Milwaukee, Wisconsin, USA. Other materials that may be useful as extenders include surfactants such as alkyl ethoxylates, for example, Neodol ™ 91-2.5 supplied by Shell Chemicals of Houston, Texas, USA. These surfactants can function as additional cleaning ingredients and as extenders.
Optional / Additional Ingredients Although not essential for the purposes of the present invention, the non-limiting list of additional ingredients illustrated hereafter are suitable for use in the present photobleaching compositions and can be desirably incorporated into preferred embodiments of the invention, by example to help or improve cleaning performance, to treat the substrate to be cleaned, or to modify the aesthetic characteristics of the photobleaching composition as is the case with perfumes, dyes, dyes or the like. The precise nature of these additional components and the levels of their incorporation will depend on the physical form of the composition and the type of cleaning operation in which they will be used. Suitable additional materials include, but not limited to, additional bleach activators, surfactants, additives, chelating agents, inhibitors for the transfer of dyes, dispersants, enzymes, and enzyme stabilizers, catalytic metal complexes, polymeric dispersing agents, antiredeposits clay and dirt, polishes, suds suppressors, dyes, perfumes, fabric elasticizing agents, fabric softeners, carriers, hydrotropes, process aids and / or pigments. In addition to the following discussion, suitable examples of those other additional ingredients and concentrations of use are included in U.S. Pat. num. 5,576,282, 6,306,812 B1 and 6,326,348 B1. Additional bleach activators. Suitable bleach activators that can be used in conjunction with the organic activator of the applicants include, but are not limited to, tetraacetylethylenediamine (TAED), benzoylcaprolactam (BzCL), 4-nitrobenzoylcaprolactam, 3-chlorobenzoylcaprolactam, benzoyloxybenzenesulfonate (BOBS), nonanoyloxybenzenesulfonate (NOBS) ), phenylbenzoate (PhBz), decanoyloxybenzenesulfonate (C10-OBS), benzoylvalerolactam (BZVL), octanoyloxybenzenesulfonate (C8-OBS), perhydrolyzable esters, perhydrolyzable carbonates, perhydrolyzable imides and mixtures thereof. Surfactants Preferably, the photobleaching compositions of the present invention comprise a surfactant or a surfactant system characterized in that the surfactant can be selected from nonionic and / or anionic and / or cationic and / or ampholytic and / or zwitterionic and / or semi-polar nonionic surfactants. The surfactant or surfactant system is normally present at a level of about 0.1%, preferably about 1%, more preferably about 5% by weight of the photobleaching compositions to about 99.9%, preferably about 80%, more preferably about 35%, and most preferably about 30% by weight of the photobleaching composition. Additives The photobleaching compositions of the present invention preferably comprise one or more additives or detergent additive systems. When present, the compositions will usually comprise at least about 1% additive, preferably at least about 5%, more preferably about 10% to about 80%, preferably about 50%, more preferably about 30% by weight of the photobleaching composition. The additives include, but are not limited to, alkali metal, ammonium and alkanolammonium salts of polyphosphates, alkali metal silicates, alkali metal and alkaline earth metal carbonates, aluminosilicate additives, polycarboxylate compounds, ether hydroxy polycarboxylates, maleic anhydride copolymers with ethylene or vinyl methyl ether, 1,3,5-trihydroxy benzene-2,4,6-trisulfonic acid and carboxymethyloxysuccinic acid, the various alkali metal, ammonium and substituted ammonium salts of polyacetic acids such as ethylenediaminetetraacetic acid and nitrilotriacetic acid, as well as polycarboxylates such as mellitic acid, succinic acid, oxydisuccinic acid, polymaleic acid, 1, 3,5-tricarboxylic acid, carboxymethyloxysuccinic acid, and the soluble salts thereof. Chelating agents. The photobleaching compositions of the present invention may also optionally contain one or more copper, iron and / or manganese chelating agents. Chelating agents, if used, will generally comprise about 0.1%, more preferably from about 3.0% to about 15% by weight of the photobleaching composition. Dye transfer inhibiting agents. The photobleaching compositions of the present invention may also include one or more dye transfer inhibiting agents. Suitable polymeric dye transfer inhibiting agents include, but are not limited to polyvinylpyrrolidone polymers, polyamine N-oxide polymers, copolymers of N-vinylpyrrolidone and N-vinylimidazole, polyvinyloxazolidones and polyvinylimidazoles or mixtures thereof. The dye transfer inhibiting agents, when present in the photobleaching compositions of the present invention, are at levels of about 0.0001%, more preferably about 0.01%, and most preferably about 0.0% by weight of the photobleaching compositions at about 10%, more preferably about 2%, and most preferably about 1% by weight of the photobleaching composition.
Dispersants The photobleaching compositions of the present invention may also contain dispersants. Suitable organic water-soluble salts are homo- or co-polymeric acids or their salts, in which the polycarboxylic acid comprises at least two carboxyl radicals separated from one another by not more than two carbon atoms. Enzymes The photobleaching compositions may comprise one or more enzymes that provide cleansing performance and / or fabric care benefits. Examples of suitable enzymes include, but are not limited to, hemicellulases, peroxidases, proteases, cellulases, xylanases, lipases, phospholipases, esterases, cutinases, pectinases, keratinases, reductases, oxidases, phenoloxidases, lipoxygenases, ligninases, pullulanases, tanases, pentosanases , malanases, ß-glucanases, arabinosidases, hyaluronidase, chondroitinase, laccase and known amylases, or mixtures thereof. Enzyme stabilizers. Enzymes for use in detergents can be stabilized by various techniques including the use of water soluble sources of calcium and / or magnesium ions in the photobleaching compositions. Bleach-reinforcing compounds. The photobleaching compositions of the present invention may comprise one or more bleach booster compounds such as a dioxirane, an oxaziridine, or an oxaziridinium or compounds capable of forming these species in place.
Among the bleach booster compounds suitable for use in accordance with the present invention are cationic, zwitterionic imines, anionic and / or polyionic mines having a net charge of about +3 to about -3, and mixtures of these. These imine bleach booster compounds of the present invention include those of the general structure:
Formula I where, for the aforementioned Formula I, R1-R4 can be a hydrogen or an unsubstituted or substituted radical selected from the group consisting of phenyl, aryl, heterocyclic ring, alkyl or cycloalkyl radicals. Among the preferred bleach booster compounds are the zwitterionic bleach boosters, which are described in U.S. Pat. num. 5,576,282 and 5,718,614. Other bleach booster compounds include cationic bleach boosters such as those described in U.S. Pat. num. 5,360,569, and 5,370,826. Catalytic metal complexes. The photobleaching compositions of the applicants may include catalytic metal complexes. One type of metal-based bleach catalyst is a catalyst system comprising a transition metal cation of defined bleach catalyst activity such as copper, iron, titanium, ruthenium, tungsten, molybdenum or manganese cations, an auxiliary metal cation of low activity or without catalytic bleaching activity such as zinc or aluminum cations, and a sequestrant with defined stability constants for the catalytic and auxiliary metal cations, especially ethylenediaminetetraacetic acid, ethylenediaminetetra (methylene) phosphonic acid and water soluble salts of the same. These catalysts are described in U.S. Pat. 4,430,243. The photobleaching compositions herein, if desired, can be catalyzed by a manganese compound. These compounds and concentrations of use are well known in the industry and include, for example, the manganese-based catalysts described in U.S. Pat. no. 5,576,282. Cobalt bleach catalysts are known, and are described, for example, in U.S. Pat. num. 5,597,936 and 5,595,967. The compositions herein may also suitably include a transition metal complex of a macropolycyclic rigid ligand - by its abbreviation "MRL". As a practical matter, and not by way of limitation, the photobleaching compositions and the cleaning processes of the present invention can be adjusted to provide about at least one part per one hundred million active MRL species in the aqueous wash medium, and preferably provide from about 0.005 ppm to about 25 ppm, more preferably from about 0.05 ppm to about 10 ppm, and most preferably from about 0.1 ppm to about 5 ppm, of the MRL in the wash solution. Preferred transition metals in the transition metal bleach catalyst include manganese, iron and chromium. Preferred MRLs herein are a special type of ultra rigid ligand that is a bridge, such as 5,12-diethyl-1, 5,8,12-tetraazabicyclo [6.6.2] hexadecane. Suitable MRLs of transition metals are prepared rapidly by known procedures such as those described, for example, in WO 00/332601 and in U.S. Pat. no. 6,225,464.
Test methods Light absorbance test (Process to determine the wavelength of light absorbed by a photosensitizer) 1.) Dissolve a sufficient quantity of a photosensitizer selected from the chosen solvent to obtain a maximum absorbance, between 250 nanometers and 700 nanometers , of 1. 2.) For the purposes of this invention, any wavelength of light characterized in that said photosensitizer has an absorbance of 0.01 is considered to be a wavelength absorbed by the photosensitizer EXAMPLES
EXAMPLE 1
The following bleaching composition is prepared by combining sulfonated zinc phthalocyanine, imidazole and the additional cleaning ingredients while avoiding exposure to light. Sulfonated zinc phthalocyanine 0.1% Imidazole 1% Additional cleaning ingredients csp 100 grams of the bleaching composition described above is added to 30 liters of aqueous washing solution in a suitable washing machine and the washing solution is illuminated with a light source which emits in at least one of the absorbance peaks of the sulfonated zinc phthalocyanine while stirring for a period of 15 minutes. The washing solution is removed and the fabrics are rinsed.
EXAMPLE 2
The following bleaching composition is prepared by combining silicon phthalocyanine-di-isoPEG 384, benzofurancarboxylic acid and cleaning adjuvants while avoiding exposure to light.
Silica phthalocyanine di-isoPEG 384 0.01% Benzofurancarboxylic acid 0.5% Additional cleaning ingredients qs 100 grams of the bleaching composition described above are added to 30 liters of aqueous washing solution in a suitable washing machine and the washing solution is illuminated with a light source emitting in at least one of the absorbance peaks of the phthalocyanine of silicon-di-isoPEG 384 while stirring for a period of 15 minutes. The washing solution is removed and the fabrics are rinsed.
EXAMPLE 3
The following bleaching composition is prepared by combining
Acridinecarboxylic acid, 2-furoic acid and additional cleaning ingredients while avoiding exposure to light.
Acridinecarboxylic acid 0 5% 2-furoacetic acid 5% Additional cleaning ingredients csp 100 grams of the bleaching composition described above are added to 30 liters of aqueous washing solution in a suitable washing machine
and the wash solution is illuminated with a light source emitting in at least one of the absorbance peaks of the acridinecarboxylic acid while stirring for a period of 15 minutes. The washing solution is removed and the fabrics are rinsed.
EXAMPLE 4
The following bleaching composition is prepared by combining
9-Fluorenone-1-carboxylic acid, 5-benzimidazolecarboxylic acid and the
Additional cleaning ingredients while avoiding exposure to light
9-Fluorenone-1-carboxylic acid 0 1% 5-Benz? M? Dazolcarboxylic acid 1% Additional cleaning ingredients csp 100 grams of the bleaching composition described above are added to 30 liters of aqueous washing solution in one Proper washing machine and washing solution is illuminated with a light source emitting in at least one of the absorbance peaks of 9-fluorenone-1-carboxylic acid while stirring for a period of 15 minutes. The washing solution is removed and the fabrics are rinsed. While particular embodiments of the present invention have been illustrated and described, it will be apparent to those skilled in the art that various changes and modifications can be made without departing from the spirit and scope of the invention. It has been intended, therefore, to cover in the appended claims all changes and modifications that are within the scope of the invention.
Claims (9)
1. A photobleaching composition comprising, on the basis of the total weight of the composition: a.) A photosensitizer soluble in water; b.) an extender; and c.) any balance of the photobleaching composition is a material selected from an aqueous liquid, an additional ingredient or mixtures thereof.
2. The photobleaching composition according to claim 1, further characterized in that it comprises, based on the total weight of the composition: a.) From 0.1% to 50%, preferably from 1% to 25%, more preferably 5%. % to 20% of the water-soluble photosensitizer; and b.) from 1% to 99.9%, preferably from 5% to 90%, more preferably from 0% to 5% of the extender.
3. The photobleaching composition according to claim 1, further characterized in that it comprises, based on the total weight of the composition: a.) From 1 ppm to 1000 ppm, preferably from 5 ppm to 500 ppm, more preferably 10 ppm. ppm to 300 ppm of the water-soluble photosensitizer; b.) from 100 ppm to 10,000 ppm, preferably from 200 ppm to 5000 ppm, more preferably from 500 ppm to 2000 ppm of the extender; and c.) the balance of the photobleaching compositions is an aqueous liquid, and optionally an additional ingredient.
4. The photobleaching composition according to any of the preceding claims, further characterized in that: a.) The water-soluble photosensitizer is selected from the group consisting of porphyrins, phthalocyanines, aromatic C8-C70, photosensitizers of superoxide, and mixtures thereof, preferably the water-soluble photosensitizer is selected from the group consisting of sulfonated zinc phthalocyanine, sulfonated aluminum phthalocyanine, silicon phthalocyanine-di-isoPEG 384, pyrene sulfonic acid, and mixtures thereof; b.) the extender is selected from the group consisting of furan, substituted furans, alkyl ethoxylates, polyethoxylates, alkyl polyethoxylates, polynuclear aromatics, imidazole, substituted imidazoles, pyrroles, substituted pyrroles, and mixtures thereof, preferably the extender is selected from the group formed by alkyl ethoxylates, imidazole, 2,5-dimethylfuran, 2-furoic acid, 3-furoic acid, and mixtures thereof. The photobleaching composition according to any of the preceding claims, further characterized in that the composition is a solid or liquid comprising an aqueous liquid. 6. The photobleaching composition according to any of the preceding claims, further characterized in that the extender comprises a surfactant. 7. A method for cleaning and / or bleaching a fabric or surface comprising the steps of; a.) provide the photobleaching composition of any preceding claim with sufficient oxygen so that the photobleaching composition comprises oxygen at a level of 1 x 10 ~ 9 moles per liter of the photobleaching composition and sufficient light energy to generate the whitening species, preferably the light energy is, based on the light that has a wavelength that is absorbed by the photosensitizer used, enough to produce more than 1 x 10"4 milliwatts / square meter of the surface of the solution exposed to light; preferably the light energy is provided by a light source located in or on a suitable household appliance for cleaning and / or bleaching a fabric or surface, and b) contacting a fabric or surface with the photobleaching composition during or after generating the bleaching species c) optionally rinsing and / or washing the fabric or surface 8. A process for making a composition otoblanking, the process comprises the step of combining a water-soluble photosensitizer, an extender and optionally a material selected from an aqueous liquid, an additional ingredient or mixtures thereof to form the photobleaching composition. 9. The process according to claim 8, further characterized in that the water-soluble photosensitizer, an extender and optionally a material selected from an aqueous liquid, an additional ingredient or mixtures thereof are combined in such a manner that the water-soluble photosensitizer, an extender and optionally a material selected from a aqueous liquid, an additional ingredient or mixtures of these are exposed to less than 1 milliwatt of light, which has a wavelength absorbed by the water-soluble photosensitizer, per square meter of the surface of the solution exposed to light and oxygen. so that the resulting mixture comprises less than 1 x 10"2 moles of oxygen per liter.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US58270504P | 2004-06-24 | 2004-06-24 | |
PCT/US2005/022438 WO2006002363A1 (en) | 2004-06-24 | 2005-06-24 | Photo bleach compositions |
Publications (1)
Publication Number | Publication Date |
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MXPA06014932A true MXPA06014932A (en) | 2007-02-28 |
Family
ID=34972863
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MXPA06014932A MXPA06014932A (en) | 2004-06-24 | 2005-06-24 | Photo bleach compositions. |
Country Status (5)
Country | Link |
---|---|
US (1) | US20050288200A1 (en) |
EP (1) | EP1758977A1 (en) |
CN (1) | CN1981024A (en) |
MX (1) | MXPA06014932A (en) |
WO (1) | WO2006002363A1 (en) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101501173B (en) * | 2006-01-23 | 2011-12-14 | 宝洁公司 | Enzyme and photobleach containing compositions |
CA2635947A1 (en) * | 2006-01-23 | 2007-08-02 | The Procter & Gamble Company | Enzyme and photobleach containing compositions |
US20150210964A1 (en) * | 2014-01-24 | 2015-07-30 | The Procter & Gamble Company | Consumer Product Compositions |
US9834740B2 (en) * | 2014-01-24 | 2017-12-05 | The Procter & Gamble Company | Photoactivators |
CN105940093B (en) * | 2014-01-31 | 2019-02-15 | 巴斯夫欧洲公司 | Ethoxylation Al or the Zn- phthalocyanine compound of ortho position substitution is in laundry detergent as the purposes of optical white |
CN108659991A (en) * | 2018-05-29 | 2018-10-16 | 点铂医疗科技(常州)有限公司 | A kind of peroxide composite material and preparation method |
GB201903318D0 (en) * | 2019-03-11 | 2019-04-24 | Reckitt Benckiser Finish Bv | Product |
EP3805346B1 (en) * | 2019-10-08 | 2024-08-14 | The Procter & Gamble Company | A method of laundering fabric |
Family Cites Families (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1408144A (en) * | 1972-06-02 | 1975-10-01 | Procter & Gamble Ltd | Bleaching process |
CA1064797A (en) * | 1975-04-03 | 1979-10-23 | Brandon H. Wiers | Photoactivated bleach-compositions and process |
GR65653B (en) * | 1978-01-11 | 1980-10-16 | Procter & Gamble | Composition for combined washing and whitening cloths |
EP0003371A1 (en) * | 1978-01-11 | 1979-08-08 | THE PROCTER & GAMBLE COMPANY | Composition containing a cationic substance and a photoactivator for improved washing and bleaching of fabrics |
CA1104451A (en) * | 1978-02-28 | 1981-07-07 | Manuel Juan De Luque | Detergent bleach composition and process |
IN153407B (en) * | 1979-09-28 | 1984-07-14 | Ciba Geigy Ag | |
GR76237B (en) * | 1981-08-08 | 1984-08-04 | Procter & Gamble | |
US5370826A (en) * | 1993-11-12 | 1994-12-06 | Lever Brothers Company, Division Of Conopco, Inc. | Quaternay oxaziridinium salts as bleaching compounds |
US5360569A (en) * | 1993-11-12 | 1994-11-01 | Lever Brothers Company, Division Of Conopco, Inc. | Activation of bleach precursors with catalytic imine quaternary salts |
US5534179A (en) * | 1995-02-03 | 1996-07-09 | Procter & Gamble | Detergent compositions comprising multiperacid-forming bleach activators |
US5597936A (en) * | 1995-06-16 | 1997-01-28 | The Procter & Gamble Company | Method for manufacturing cobalt catalysts |
US5916481A (en) * | 1995-07-25 | 1999-06-29 | The Procter & Gamble Company | Low hue photobleaches |
US5718614A (en) * | 1995-08-28 | 1998-02-17 | Electro-Matic Products Company | Control apparatus for grinder |
US5576282A (en) * | 1995-09-11 | 1996-11-19 | The Procter & Gamble Company | Color-safe bleach boosters, compositions and laundry methods employing same |
MA24136A1 (en) * | 1996-04-16 | 1997-12-31 | Procter & Gamble | MANUFACTURE OF SURFACE AGENTS. |
JP2001509191A (en) * | 1997-01-24 | 2001-07-10 | ザ、プロクター、エンド、ギャンブル、カンパニー | Photochemical superoxide generator |
WO1998039335A1 (en) * | 1997-03-07 | 1998-09-11 | The Procter & Gamble Company | Improved methods of making cross-bridged macropolycycles |
JP4489190B2 (en) * | 1997-03-07 | 2010-06-23 | ザ、プロクター、エンド、ギャンブル、カンパニー | Bleach composition containing metal bleach catalyst and bleach activator and / or organic percarboxylic acid |
GB2329397A (en) * | 1997-09-18 | 1999-03-24 | Procter & Gamble | Photo-bleaching agent |
US7345016B2 (en) * | 2003-06-27 | 2008-03-18 | The Procter & Gamble Company | Photo bleach lipophilic fluid cleaning compositions |
-
2005
- 2005-05-16 US US11/130,327 patent/US20050288200A1/en not_active Abandoned
- 2005-06-24 EP EP05766600A patent/EP1758977A1/en not_active Withdrawn
- 2005-06-24 WO PCT/US2005/022438 patent/WO2006002363A1/en not_active Application Discontinuation
- 2005-06-24 MX MXPA06014932A patent/MXPA06014932A/en unknown
- 2005-06-24 CN CNA2005800209355A patent/CN1981024A/en active Pending
Also Published As
Publication number | Publication date |
---|---|
EP1758977A1 (en) | 2007-03-07 |
CN1981024A (en) | 2007-06-13 |
WO2006002363A1 (en) | 2006-01-05 |
US20050288200A1 (en) | 2005-12-29 |
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