JP2011506788A - How to treat the dough - Google Patents
How to treat the dough Download PDFInfo
- Publication number
- JP2011506788A JP2011506788A JP2010537346A JP2010537346A JP2011506788A JP 2011506788 A JP2011506788 A JP 2011506788A JP 2010537346 A JP2010537346 A JP 2010537346A JP 2010537346 A JP2010537346 A JP 2010537346A JP 2011506788 A JP2011506788 A JP 2011506788A
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- Prior art keywords
- polymer
- dough
- aqueous medium
- polymers
- copolymers
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 229920000642 polymer Polymers 0.000 claims abstract description 122
- 239000012736 aqueous medium Substances 0.000 claims abstract description 46
- 238000000034 method Methods 0.000 claims abstract description 35
- 229920001519 homopolymer Polymers 0.000 claims abstract description 33
- 229920001577 copolymer Polymers 0.000 claims abstract description 31
- 150000001720 carbohydrates Chemical class 0.000 claims abstract description 17
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 claims abstract description 13
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims abstract description 13
- -1 alkylene glycol Chemical compound 0.000 claims abstract description 11
- 125000002947 alkylene group Chemical group 0.000 claims abstract description 9
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims abstract description 9
- 239000000203 mixture Substances 0.000 claims description 27
- 229920002125 Sokalan® Polymers 0.000 claims description 12
- 150000001735 carboxylic acids Chemical class 0.000 claims description 12
- 239000003792 electrolyte Substances 0.000 claims description 12
- 230000002378 acidificating effect Effects 0.000 claims description 10
- 239000004584 polyacrylic acid Substances 0.000 claims description 8
- 238000011282 treatment Methods 0.000 claims description 8
- 230000008569 process Effects 0.000 claims description 6
- 239000007864 aqueous solution Substances 0.000 claims description 5
- 239000003945 anionic surfactant Substances 0.000 claims description 4
- 239000002609 medium Substances 0.000 claims description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract description 8
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 abstract description 5
- 239000004744 fabric Substances 0.000 description 37
- 230000008021 deposition Effects 0.000 description 15
- 238000004140 cleaning Methods 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 230000000052 comparative effect Effects 0.000 description 13
- 229920000742 Cotton Polymers 0.000 description 9
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 9
- 239000002689 soil Substances 0.000 description 9
- 239000000463 material Substances 0.000 description 8
- 229920000728 polyester Polymers 0.000 description 8
- 229920002451 polyvinyl alcohol Polymers 0.000 description 8
- 239000002304 perfume Substances 0.000 description 7
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 7
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 7
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
- 239000003599 detergent Substances 0.000 description 6
- 238000005406 washing Methods 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- 239000004372 Polyvinyl alcohol Substances 0.000 description 5
- 230000009286 beneficial effect Effects 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- 239000003153 chemical reaction reagent Substances 0.000 description 5
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 5
- 239000004071 soot Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 229920001515 polyalkylene glycol Polymers 0.000 description 4
- 229920001223 polyethylene glycol Polymers 0.000 description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 125000001033 ether group Chemical group 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 3
- 239000011976 maleic acid Substances 0.000 description 3
- 229910000029 sodium carbonate Inorganic materials 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- 229910002651 NO3 Inorganic materials 0.000 description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 150000004996 alkyl benzenes Chemical class 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000001110 calcium chloride Substances 0.000 description 2
- 229910001628 calcium chloride Inorganic materials 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 235000010980 cellulose Nutrition 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000007850 fluorescent dye Substances 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 229920005615 natural polymer Polymers 0.000 description 2
- 229920000233 poly(alkylene oxides) Polymers 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 229920001059 synthetic polymer Polymers 0.000 description 2
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 240000000491 Corchorus aestuans Species 0.000 description 1
- 235000011777 Corchorus aestuans Nutrition 0.000 description 1
- 235000010862 Corchorus capsularis Nutrition 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 1
- 229920006397 acrylic thermoplastic Polymers 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 229920013820 alkyl cellulose Polymers 0.000 description 1
- 125000000217 alkyl group Chemical class 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 125000002843 carboxylic acid group Chemical group 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 239000002781 deodorant agent Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 239000012771 household material Substances 0.000 description 1
- 239000000017 hydrogel Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 229920013821 hydroxy alkyl cellulose Chemical class 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L magnesium chloride Substances [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229920001206 natural gum Polymers 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920000191 poly(N-vinyl pyrrolidone) Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920001444 polymaleic acid Polymers 0.000 description 1
- 229920001184 polypeptide Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M potassium chloride Inorganic materials [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 239000008213 purified water Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000003716 rejuvenation Effects 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 238000005204 segregation Methods 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Inorganic materials [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- KWVISVAMQJWJSZ-VKROHFNGSA-N solasodine Chemical compound O([C@@H]1[C@@H]([C@]2(CC[C@@H]3[C@@]4(C)CC[C@H](O)CC4=CC[C@H]3[C@@H]2C1)C)[C@@H]1C)[C@]11CC[C@@H](C)CN1 KWVISVAMQJWJSZ-VKROHFNGSA-N 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/01—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with natural macromolecular compounds or derivatives thereof
- D06M15/03—Polysaccharides or derivatives thereof
-
- 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
- C11D3/20—Organic compounds containing oxygen
- C11D3/22—Carbohydrates or derivatives thereof
- C11D3/222—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
-
- 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
- C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3707—Polyethers, e.g. polyalkyleneoxides
-
- 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
- C11D3/3753—Polyvinylalcohol; Ethers or esters thereof
-
- 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
-
- 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
- C11D3/3769—(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines
- C11D3/3776—Heterocyclic compounds, e.g. lactam
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/01—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with natural macromolecular compounds or derivatives thereof
- D06M15/03—Polysaccharides or derivatives thereof
- D06M15/05—Cellulose or derivatives thereof
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/01—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with natural macromolecular compounds or derivatives thereof
- D06M15/03—Polysaccharides or derivatives thereof
- D06M15/05—Cellulose or derivatives thereof
- D06M15/09—Cellulose ethers
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/263—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/327—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated alcohols or esters thereof
- D06M15/333—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated alcohols or esters thereof of vinyl acetate; Polyvinylalcohol
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/356—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of other unsaturated compounds containing nitrogen, sulfur, silicon or phosphorus atoms
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/356—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of other unsaturated compounds containing nitrogen, sulfur, silicon or phosphorus atoms
- D06M15/3562—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of other unsaturated compounds containing nitrogen, sulfur, silicon or phosphorus atoms containing nitrogen
-
- C11D2111/12—
Abstract
本発明では、水性媒体中のポリマーA及びBと生地を接触させる工程を含む生地の処理方法が提供され、ここで
(a)ポリマーAはビニルアルコール、アルキレングリコール、サッカリド、及びカルボン酸のホモポリマーまたはコポリマーからなるクラスから選択され;及び
(b)ポリマーBはビニルピロリドン、アルキレンオキシド、サッカリド、及びカルボン酸のホモポリマーまたはコポリマーからなるクラスから選択され;
ポリマーA及びBは同じクラスのものではなく、水性媒体は6未満のpHを有する。The present invention provides a method for treating a dough comprising the step of contacting the dough with polymers A and B in an aqueous medium, wherein (a) polymer A is a homopolymer of vinyl alcohol, alkylene glycol, saccharide, and carboxylic acid. Or (b) polymer B is selected from the class consisting of homopolymers or copolymers of vinyl pyrrolidone, alkylene oxide, saccharide, and carboxylic acid;
Polymers A and B are not of the same class and the aqueous medium has a pH of less than 6.
Description
本発明は、生地の処理方法に関する。本発明は更に、生地の処理のための組成物及びキットに関する。本発明は、この応用を参考にして以下に記載されるであろう。しかしながら本発明は、この特定の使用分野に制限されないことが予測されるであろう。 The present invention relates to a dough processing method. The invention further relates to compositions and kits for the treatment of dough. The invention will be described below with reference to this application. However, it will be appreciated that the invention is not limited to this particular field of use.
本明細書を通じて従来技術のいずれの議論も、そのような従来技術が広く既知であること、または当該技術分野の一般的な共通の知見を形成することを認めるものとして、いずれの態様でも考慮されるべきではない。 Any discussion of the prior art throughout this specification will be considered in any manner as an admission that such prior art is widely known or forms common common knowledge in the art. Should not.
US2006046950A(Penninger及びBastigkeit, 2006)は、汚れ放出可能なアルキルまたはヒドロキシアルキルセルロース誘導体と、ポリペプチド、ヒドロゲル、ポリビニルアルコール、ポリアルキレングリコール、並びにアクリル酸、メタクリル酸、及びマレイン酸のホモポリマー、並びにアクリル酸、メタクリル酸、及びマレイン酸のコポリマー、並びに前記ホモポリマーとコポリマーとの混合物からなるクラスから選択される吸湿性ポリマーとの組み合わせを含む、生地材料の洗浄用洗剤組成物を教示している。セルロース誘導体と組み合わせた吸湿性ポリマーの使用は、改良された洗浄特性を導くと開示されている。 US2006604950A (Penninger and Bastigkeit, 2006) describes soil-releasing alkyl or hydroxyalkyl cellulose derivatives and polypeptides, hydrogels, polyvinyl alcohol, polyalkylene glycols, and homopolymers of acrylic acid, methacrylic acid, and maleic acid, and acrylics. A detergent composition for washing fabric materials comprising a copolymer of acids, methacrylic acid and maleic acid and a combination of hygroscopic polymers selected from the class consisting of mixtures of said homopolymers and copolymers. The use of hygroscopic polymers in combination with cellulose derivatives is disclosed to lead to improved cleaning properties.
EP025696(Unilever, 1988)は、汚れ懸濁物の改良が、洗剤組成物にビニルピロリドンポリマーと非イオン性セルロースエーテルとの混合物を添加することによって達成されることを教示している。 EP 025696 (Unilever, 1988) teaches that the improvement of soil suspension is achieved by adding a mixture of vinylpyrrolidone polymer and nonionic cellulose ether to the detergent composition.
GB994353(Domestos, 1965)は、特定のポリマー材料の混合物が、合成表面活性剤に基づく未成熟の洗剤組成物に取り込まれた際に、同じ洗浄組成物に単独で添加された際の個々のポリマー単独の活性と比較して、増大した抗再析を提供することを教示している。 GB 994353 (Domestos, 1965) describes individual polymers when a mixture of specific polymeric materials is added alone to the same cleaning composition when incorporated into an immature detergent composition based on a synthetic surfactant. It teaches providing increased anti-re-segregation compared to single activity.
US3771951(Berni等, 1973)及びGB133803(Gaf Corp, 1973)は、水溶性界面活性剤、及び水溶性ポリビニルアルコールと水溶性ポリビニルピロリドンとの混合物を含む洗剤組成物が、汚れ懸濁物の増大した度合いを示すことを教示している。 US3771951 (Berni et al., 1973) and GB133803 (Gaf Corp, 1973) show that a detergent composition comprising a water-soluble surfactant and a mixture of water-soluble polyvinyl alcohol and water-soluble polyvinylpyrrolidone has increased soil suspension. Teaching to show the degree.
上述の方法は、汚れの改良された抗再析と生地の良好な洗浄を提供することを報告している。しかしながら、生地のその後の水洗い後の汚れの減少は報告されていない。更に、前記洗浄組成物は、界面活性剤を必須に含み、先浄水のpHはアルカリ性または中性である。 The method described above has been reported to provide improved anti-re-deposition of soil and good cleaning of the fabric. However, no reduction in soiling after subsequent water washing of the fabric has been reported. Further, the cleaning composition essentially includes a surfactant, and the pH of the pre-purified water is alkaline or neutral.
US4007305(Kahar等, 1977)は、最適な汚れの放出と汚れの撥水特性を与える生地に対する満足な耐久性のない仕上がりを提供するという問題に応えている。この文献によれば、7.5−11のpH値を有し、カルボン酸基を有する水溶性親水性汚れ放出ポリマーと、分散した疎水性汚れ撥水性フルオロケミカルを含むアルカリ水性媒体で処理しなければならない。 US4007305 (Kahar et al., 1977) addresses the problem of providing a satisfactory unfinished finish for fabrics that provides optimal soil release and soil water repellency. According to this document, it must be treated with an aqueous alkaline medium having a pH value of 7.5-11 and containing a water-soluble hydrophilic soil release polymer having a carboxylic acid group and a dispersed hydrophobic soil water-repellent fluorochemical. I must.
他方で、生地の変性のための各種の工業的処理が、汚れに対して生地をより感受性にすることが知られている。このタイプの生地の変性は、通常生地の製造の間で実施される。この処理は、基質特異的であることに加えて、家庭で実施することが比較的困難である。 On the other hand, various industrial treatments for fabric modification are known to make the fabric more susceptible to soiling. This type of dough modification is usually performed during the manufacture of the dough. In addition to being substrate specific, this treatment is relatively difficult to carry out at home.
従来技術の欠点に鑑みて、本発明の目的の一つは、家庭で容易に使用できる生地の汚れを減少する方法を提供することである。 In view of the shortcomings of the prior art, one of the objects of the present invention is to provide a method of reducing fabric soiling that can be easily used at home.
本発明の別の目的は、生地の汚れを減少するための生地の処理方法を提供することである。 Another object of the present invention is to provide a method of treating a dough to reduce the soiling of the dough.
本発明のまた別の目的は、その後の洗浄の効力を改善する生地の処理方法を提供することである。 Yet another object of the present invention is to provide a method of treating a dough that improves the efficacy of subsequent washing.
本発明のまた別の目的は、香料や蛍光剤といった有益な薬剤の増大した沈着を可能にする生地の汚れの減少方法を提供することである。 Yet another object of the present invention is to provide a method for reducing fabric soiling that allows for increased deposition of beneficial agents such as perfumes and fluorescent agents.
本発明のまた別の目的は、コットン、ポリエステル、及びポリコットンといった各種のタイプの生地で有効である生地の処理方法を提供することである。 Yet another object of the present invention is to provide a method for treating fabrics that is effective with various types of fabrics such as cotton, polyester, and polycotton.
本発明のまた別の目的は、家庭で実施するのが比較的容易である生地の処理方法を提供することである。 Another object of the present invention is to provide a method for treating a fabric that is relatively easy to implement at home.
本発明者は驚くべきことに、一方が複数のヒドロキシル基を含み、他方が複数のカルボニル基またはエーテル基を含む二種類の異なるポリマーを有する酸性のpHを有する水性媒体と生地を接触させることが、ポリマーの沈着を増大し、汚れの減少、その後の洗浄の容易性、及び有益な試薬の増大した沈着のような利益を与えることを見出した。 The inventor has surprisingly contacted the dough with an aqueous medium having an acidic pH with two different polymers, one containing multiple hydroxyl groups and the other containing multiple carbonyl or ether groups. It has been found that it provides benefits such as increased polymer deposition, reduced soiling, ease of subsequent cleaning, and increased deposition of beneficial reagents.
本発明の第一の特徴点によれば、水性媒体中のポリマーA及びBと生地を接触させる工程を含む生地の処理方法が提供され、ここで
(a)ポリマーAはビニルアルコール、アルキレングリコール、サッカリド、及びカルボン酸のホモポリマーまたはコポリマーからなるクラスから選択され;及び
(b)ポリマーBはビニルピロリドン、アルキレンオキシド、サッカリド、及びカルボン酸のホモポリマーまたはコポリマーからなるクラスから選択され;
ポリマーA及びBは同じクラスのものではなく、水性媒体は6未満のpHを有する。
According to a first aspect of the present invention, there is provided a method for treating a dough comprising the step of contacting the dough with polymers A and B in an aqueous medium, wherein (a) polymer A comprises vinyl alcohol, alkylene glycol, Selected from the class consisting of saccharides and homopolymers or copolymers of carboxylic acids; and (b) polymer B is selected from the class consisting of homopolymers or copolymers of vinylpyrrolidone, alkylene oxides, saccharides and carboxylic acids;
Polymers A and B are not of the same class and the aqueous medium has a pH of less than 6.
本発明の第二の特徴点によれば、1から99重量%のポリマーA、1から99重量%のポリマーB、及び0から10重量%の酸性成分を含む生地の処理のための組成物が提供され、ここで
(a)ポリマーAはビニルアルコール、アルキレングリコール、サッカリド、及びカルボン酸のホモポリマーまたはコポリマーからなるクラスから選択され;及び
(b)ポリマーBはビニルピロリドン、アルキレンオキシド、サッカリド、及びカルボン酸のホモポリマーまたはコポリマーからなるクラスから選択され;
ポリマーA及びBは同じクラスのものではなく、前記組成物の1%水溶液のpHは6未満である。
According to a second aspect of the invention, there is provided a composition for treating a dough comprising 1 to 99% by weight of Polymer A, 1 to 99% by weight of Polymer B, and 0 to 10% by weight of an acidic component. Wherein (a) polymer A is selected from the class consisting of homopolymers or copolymers of vinyl alcohol, alkylene glycol, saccharide, and carboxylic acid; and (b) polymer B is vinyl pyrrolidone, alkylene oxide, saccharide, and Selected from the class consisting of homopolymers or copolymers of carboxylic acids;
Polymers A and B are not of the same class and the pH of a 1% aqueous solution of the composition is less than 6.
本発明の第三の特徴点によれば、第二の特徴点の組成物と、使用のための一連の説明書とを含む生地の処理のためのキットが提供される。 According to a third aspect of the present invention, there is provided a kit for treating a dough comprising the composition of the second aspect and a set of instructions for use.
生地
処理できる生地は、合成並びに天然の繊維を含む。生地としては、コットン、ポリコットン、ポリエステル、シルク、またはナイロンが挙げられる。本発明の方法は、衣類及び他の布製品及び家庭の洗濯で典型的な洗濯物を形成するアパレル材料を処理するために使用できる。本発明の方法に従って処理できる家庭の材料は、ベッドカバー、毛布、カーペット、カーテン、及びクッションを含むがこれらに制限されない。本発明の方法は、生地の処理のために主として記載されるが、本発明の方法は、ジュート、レザー、デニム、及びカンバスのような他の材料を処理するためにも有利には使用できると考慮される。本発明の方法は、靴、レインウェアー、及びジャケットのような製品を処理するために使用できると考慮される。
Fabrics Fabrics that can be treated include synthetic as well as natural fibers. Examples of the fabric include cotton, polycotton, polyester, silk, and nylon. The method of the present invention can be used to treat apparel materials that form laundry in clothing and other fabric products and household laundry typical of laundry. Household materials that can be treated according to the method of the present invention include, but are not limited to, bedspreads, blankets, carpets, curtains, and cushions. Although the method of the present invention is primarily described for the treatment of fabrics, the method of the present invention can be advantageously used to treat other materials such as jute, leather, denim, and canvas. Be considered. It is contemplated that the method of the present invention can be used to process products such as shoes, rainwear, and jackets.
ポリマーA
本発明によれば、ポリマーAは複数のヒドロキシル基またはカルボキシル基を有する。ポリマーAは好ましくは300から109の分子量を有する。ポリマーAは、ビニルアルコール、アルキレングリコール、サッカリド、及びカルボン酸のホモポリマーまたはコポリマーからなるクラスから選択される。
Polymer A
According to the present invention, polymer A has a plurality of hydroxyl groups or carboxyl groups. Polymer A preferably has a molecular weight of 300 from 109. Polymer A is selected from the class consisting of homopolymers or copolymers of vinyl alcohol, alkylene glycols, saccharides, and carboxylic acids.
本発明に係るポリマーAのある非制限的な例は、以下のものを含む:
(a)ビニルアルコールまたはポリビニルアルコールのホモポリマー;
(b)エチレングリコールまたはプロピレングリコールのホモポリマー、即ちポリエチレングリコール及びポリプロピレングリコール;
(c)カルボン酸のホモポリマー、即ちポリカルボン酸、例えばポリアクリル酸、ポリマレイン酸、またはアクリル酸とマレイン酸のコポリマー;
(d)ポリサッカリド、例えばデンプン、セルロース、アルギン酸ナトリウム、天然ゴム、及びそれらの変性材料、例えばナトリウムカルボキシメチルセルロース、ヒドロキシエチルセルロース。
Some non-limiting examples of polymer A according to the present invention include:
(A) vinyl alcohol or a homopolymer of polyvinyl alcohol;
(B) homopolymers of ethylene glycol or propylene glycol, ie polyethylene glycol and polypropylene glycol;
(C) homopolymers of carboxylic acids, ie polycarboxylic acids such as polyacrylic acid, polymaleic acid, or copolymers of acrylic acid and maleic acid;
(D) polysaccharides such as starch, cellulose, sodium alginate, natural gums and their modified materials such as sodium carboxymethylcellulose, hydroxyethylcellulose.
ビニルアルコールのホモポリマーまたはコポリマーは、好ましくは10000から1000000、より好ましくは50000から500000、最も好ましくは50000から200000の分子量を有する。使用できる市販品のポリビニルアルコールは、GOHSENOL(登録商標; Nippon Synthetic Chemical Industry)、NOWIOL(登録商標; Clariant)、及びPOVAL(登録商標; Kuraray)を含む。 The homopolymer or copolymer of vinyl alcohol preferably has a molecular weight of 10,000 to 1,000,000, more preferably 50,000 to 500,000, most preferably 50,000 to 200,000. Commercially available polyvinyl alcohols that can be used include GOHSENOL® (Nippon Synthetic Chemical Industry), NOWIOL® (Clariant), and POVAL® (Kuraray).
アルキレングリコールのホモポリマーまたはコポリマーは、好ましくは4000から20000、より好ましくは5000から15000、最も好ましくは5000から10000の分子量を有する。市販品のポリアルキレングリコールが使用できる。市販品のポリアルキレングリコールのいくつかの例は、POLYGLYKOL(登録商標; Clariant)及びCARBOWAX(登録商標; Union Carbide)を含む。 The alkylene glycol homopolymer or copolymer preferably has a molecular weight of 4000 to 20000, more preferably 5000 to 15000, and most preferably 5000 to 10,000. Commercially available polyalkylene glycol can be used. Some examples of commercially available polyalkylene glycols include POLYGLYKOL® (Clariant) and CARBOWAX® (Union Carbide).
カルボン酸のホモポリマーまたはコポリマーは、好ましくは2000から10000000、より好ましくは50000から1000000、最も好ましくは90000から500000の分子量を有する。 The carboxylic acid homopolymer or copolymer preferably has a molecular weight of 2000 to 10000000, more preferably 50000 to 1000000, most preferably 90000 to 500000.
サッカリドのホモポリマーまたはコポリマーは、好ましくは1000から109、より好ましくは10000から109、最も好ましくは100000から109の分子量を有する。 The saccharide homopolymer or copolymer preferably has a molecular weight of 1000 to 10 9 , more preferably 10,000 to 10 9 , most preferably 100,000 to 10 9 .
ポリマーAは合成であっても天然でも良い。しかしながら、合成ポリマーは天然ポリマーよりも好ましい。 Polymer A may be synthetic or natural. However, synthetic polymers are preferred over natural polymers.
好ましい特徴点によれば、ポリマーAは水溶性である。 According to a preferred feature, the polymer A is water soluble.
ポリマーAは、ビニルアルコールまたはカルボン酸のホモポリマーまたはコポリマーからなるクラスから選択されることが好ましい。 Polymer A is preferably selected from the class consisting of homopolymers or copolymers of vinyl alcohol or carboxylic acid.
カルボン酸のホモポリマーまたはコポリマーは、好ましくはポリアクリル酸またはそのコポリマーである。例として、SOKALAN(登録商標)PA(BASF)、及びCARBOPOL(登録商標; Lubrizol)が含まれる。 The homopolymer or copolymer of carboxylic acid is preferably polyacrylic acid or a copolymer thereof. Examples include SOKALAN® PA (BASF) and CARBOPOL® (Lubrizol).
ポリマーAの量は、好ましくは生地の領域(cm2)当たり0.005から2、より好ましくは0.02から1、最も好ましくは0.05から0.5mgである。 The amount of polymer A is preferably from 0.005 to 2, more preferably from 0.02 to 1, most preferably from 0.05 to 0.5 mg per area (cm 2 ) of the dough.
ポリマーB
本発明によれば、ポリマーBはエーテル基またはカルボニル基を含むモノマー単位を有する。ポリマーBは、好ましくは1000から109の分子量を有する。ポリマーBは、ビニルピロリドン、アルキレンオキシド、サッカリド、及びカルボン酸のホモポリマーまたはコポリマーからなるクラスから選択される。
Polymer B
According to the invention, the polymer B has monomer units containing ether groups or carbonyl groups. Polymer B preferably has a molecular weight of 1000 to 10 9. Polymer B is selected from the class consisting of homopolymers or copolymers of vinyl pyrrolidone, alkylene oxides, saccharides, and carboxylic acids.
カルボン酸及び/またはサッカリド及び/またはポリアルキレングリコール/エーテルのポリマー及びホモポリマーは、ヒドロキシル基またはカルボキシル基、及びカルボニル基またはエーテル基のいずれかを含むため、ポリマーAまたはポリマーBとして両者とも選択されるのに適する。しかしながら、必須の特徴点によれば、ポリマーAとポリマーBは同じクラスのものではない。ポリマーAとBが異なるクラスのポリマーから選択されることが特に好ましい。理論的に制限されたいとは思わないが、二つのポリマーAとBは、水に溶解した際、ポリマーAとBのそれぞれよりも低い溶解度を有する複合体を形成し、それが増大した沈着と他の利益に寄与すると解される。 Polymers and homopolymers of carboxylic acids and / or saccharides and / or polyalkylene glycol / ethers are either selected as polymer A or polymer B because they contain either hydroxyl or carboxyl groups and carbonyl or ether groups. Suitable for However, according to the essential features, polymer A and polymer B are not of the same class. It is particularly preferred that the polymers A and B are selected from different classes of polymers. While not wishing to be theoretically limited, the two polymers A and B, when dissolved in water, form a complex with a lower solubility than each of polymers A and B, which increases the deposition and It is understood that it contributes to other profits.
ビニルピロリドンのホモポリマーまたはコポリマーは、好ましくは1000から10000000、より好ましくは10000から1000000、最も好ましくは30000から500000の分子量を有する。市販品のポリビニルピロリドンが使用でき、その例の一つはLUVISKOL(登録商標; BASF)である。 The homopolymer or copolymer of vinylpyrrolidone preferably has a molecular weight of 1000 to 10,000,000, more preferably 10,000 to 1,000,000, and most preferably 30,000 to 500,000. Commercially available polyvinylpyrrolidone can be used, one example being LUVISKOL® (BASF).
ポリアルキレンオキシドのホモポリマーまたはコポリマーは、20000を超える分子量を有する。前記分子量は、好ましくは20000から1000000、より好ましくは30000から500000、最も好ましくは50000から200000である。 The polyalkylene oxide homopolymer or copolymer has a molecular weight greater than 20000. The molecular weight is preferably 20000 to 1000000, more preferably 30000 to 500000, and most preferably 50000 to 200000.
サッカリドのホモポリマーまたはコポリマーは、好ましくは1000から109、より好ましくは10000から109、最も好ましくは100000から109の分子量を有する。いずれかの市販品のポリアルキレンオキシド、例えばPOLYOX(登録商標; Dow Chemical Co)が本発明によって使用できる。 The saccharide homopolymer or copolymer preferably has a molecular weight of 1000 to 10 9 , more preferably 10,000 to 10 9 , most preferably 100,000 to 10 9 . Any commercially available polyalkylene oxide, such as POLYOX® (Dow Chemical Co), can be used according to the present invention.
ポリマーBは合成であっても天然でも良い。しかしながら、合成ポリマーは天然ポリマーより好ましい。 Polymer B may be synthetic or natural. However, synthetic polymers are preferred over natural polymers.
好ましい特徴点によれば、ポリマーBは水溶性である。 According to a preferred feature, the polymer B is water soluble.
ポリマーBはビニルピロリドンまたはアルキレンオキシドのホモポリマーまたはコポリマーからなるクラスから選択されることが特に好ましい。 It is particularly preferred that the polymer B is selected from the class consisting of vinylpyrrolidone or alkylene oxide homopolymers or copolymers.
ポリマーBの量は、好ましくは生地の領域(cm2)当たり0.005から2、より好ましくは0.02から1、最も好ましくは0.05から0.5mgである。 The amount of polymer B is preferably from 0.005 to 2, more preferably from 0.02 to 1, and most preferably from 0.05 to 0.5 mg per area (cm 2 ) of the dough.
特に好ましいポリマーAとポリマーBの組み合わせのいくつかの例が以下に記載される。 Some examples of particularly preferred polymer A and polymer B combinations are described below.
表1:ポリマーの好ましい組み合わせ
最も好ましいポリマーの組み合わせは、上記表1の初めの三種類、即ちPAA−PVP、PAA−PEO及びPEG−PAAのものである。 The most preferred polymer combinations are those of the first three types in Table 1 above: PAA-PVP, PAA-PEO and PEG-PAA.
水性媒体
本発明によれば、二種類のポリマーは、6未満のpHを有する水性媒体中で生地と接触される。水性媒体は、好ましくは5未満、より好ましくは4未満のpHを有する。水性媒体は、好ましくは1を超える、より好ましくは2を超えるpHを有する。
Aqueous Medium According to the present invention, the two types of polymers are contacted with the dough in an aqueous medium having a pH of less than 6. The aqueous medium preferably has a pH of less than 5, more preferably less than 4. The aqueous medium preferably has a pH greater than 1, more preferably greater than 2.
前記ポリマーが水性媒体に添加される際、水性媒体のpHは6未満である態様となるように選択されて良い。好ましくは酸性成分が水性媒体に添加されて、水性媒体のpHを6未満とするようにする。生成した水性媒体のpHを6未満に低下する酸性成分は当業者に周知であり、いずれかの適切な酸性成分が選択されて良い。 When the polymer is added to the aqueous medium, the pH of the aqueous medium may be selected to be less than 6. Preferably an acidic component is added to the aqueous medium so that the pH of the aqueous medium is less than 6. Acidic components that lower the pH of the resulting aqueous medium to less than 6 are well known to those skilled in the art, and any suitable acidic component may be selected.
水性媒体は、ポリマーAまたはポリマーBのいずれか、あるいは両者のポリマーを含んでも良い。別法として、両者のポリマーの一方は、本発明の方法の間で水性媒体に添加されても良い。
ポリマーAは、水性媒体と混合された際に、水性媒体の0.005から10重量%、より好ましくは0.05から5重量%、最も好ましくは0.05から2重量%の範囲である。
The aqueous medium may include either polymer A or polymer B, or both polymers. Alternatively, one of both polymers may be added to the aqueous medium during the process of the present invention.
Polymer A, when mixed with an aqueous medium, ranges from 0.005 to 10%, more preferably 0.05 to 5%, most preferably 0.05 to 2% by weight of the aqueous medium.
ポリマーBは、水性媒体と混合された際に、水性媒体の0.005から10重量%、より好ましくは0.01から5重量%、最も好ましくは0.01から2重量%の範囲である。 Polymer B ranges from 0.005 to 10%, more preferably from 0.01 to 5%, most preferably from 0.01 to 2% by weight of the aqueous medium when mixed with the aqueous medium.
水性媒体は、好ましくは電解質を含む。電解質は、好ましくは水性媒体の0.001から5重量%、より好ましくは0.01から1重量%、最も好ましくは0.04から0.2重量%の範囲である。 The aqueous medium preferably includes an electrolyte. The electrolyte is preferably in the range of 0.001 to 5%, more preferably 0.01 to 1%, most preferably 0.04 to 0.2% by weight of the aqueous medium.
理論によって制限されることを所望するわけではないが、電解質の添加は、本発明の方法を、比較的低量のポリマーA及びBで実施することを可能にすると解される。 While not wishing to be limited by theory, it is understood that the addition of electrolyte allows the process of the present invention to be performed with relatively low amounts of polymers A and B.
本発明によって使用できる電解質は、水溶性イオン性塩を含む。前記塩のカチオンは、アルカリ金属、アルカリ土類金属、または三価金属カチオンを含む。前記塩のアニオンは、塩化物、硫酸塩、硝酸塩、、及びリン酸塩を含む。電解質のいくつかの例は、ナトリウム、カリウム、マグネシウム、またはカルシウムの塩化物、硫酸塩、または硝酸塩を含む。カルシウム塩が特に好ましい。 Electrolytes that can be used according to the present invention include water-soluble ionic salts. The cation of the salt includes an alkali metal, alkaline earth metal, or trivalent metal cation. The salt anions include chloride, sulfate, nitrate, and phosphate. Some examples of electrolytes include sodium, potassium, magnesium, or calcium chloride, sulfate, or nitrate. Calcium salts are particularly preferred.
好ましい特徴点によれば、水性媒体は、200ppm以下のアニオン性界面活性剤を含む。水性媒体は、100ppm以下、より好ましくは50ppm未満のアニオン性界面活性剤を含む。水性媒体がアニオン性界面活性剤を実質的に含まないことが特に好ましい。 According to a preferred feature, the aqueous medium comprises 200 ppm or less of an anionic surfactant. The aqueous medium contains no more than 100 ppm, more preferably less than 50 ppm anionic surfactant. It is particularly preferred that the aqueous medium is substantially free of anionic surfactant.
水性媒体は、少なくとも一つの有益な試薬を含むことが好ましい。水性媒体に含むことができる有益な試薬は、香料、蛍光剤、脱臭剤、抗菌剤、色直し色素、青味剤のような成分を含むがこれらに限定されない。本発明の利点の一つは、有益な試薬の沈着が増大する点である。 The aqueous medium preferably includes at least one beneficial reagent. Useful reagents that can be included in the aqueous medium include, but are not limited to, ingredients such as perfumes, fluorescent agents, deodorants, antibacterial agents, rejuvenating dyes, bluing agents. One advantage of the present invention is that the deposition of beneficial reagents is increased.
方法順序
生地はポリマーA及びBと、いずれかの順序で連続的にまたは同時にのいずれかで接触されると考慮される。従って生地は、ポリマーAと接触されて、引き続きポリマーBと接触されて良い。別法として生地は、ポリマーBと接触されて、引き続きポリマーAと接触されても良い。生地は、ポリマーAとBの両者と同時に接触されても良い。生地は両者のポリマーと同時に接触されても良いが、生地はいずれかの順序で連続的にポリマーと接触されることが好ましい。
Process Order It is considered that the dough is contacted with polymers A and B either sequentially or simultaneously in either order. Thus, the dough may be contacted with polymer A and subsequently with polymer B. Alternatively, the dough may be contacted with polymer B and subsequently contacted with polymer A. The dough may be contacted simultaneously with both polymers A and B. Although the dough may be contacted simultaneously with both polymers, it is preferred that the dough is contacted with the polymer continuously in either order.
接触方法
ポリマーAとBとの生地の接触工程は、いずれかの適切な態様で実施できる。
Contacting Method The dough contacting step of polymers A and B can be performed in any suitable manner.
ポリマーAまたはポリマーBまたは両者は、生地と接触される前に水性媒体と混合される。別法として、ポリマーAは生地と接触される前にアルコール及びアセトンのような溶媒を含む非水性媒体と混合されても良い。しかしながら、ポリマーまたは両者のポリマーは、生地と接触される前に水性媒体と混合されることが好ましい。生地は、一つ以上のポリマーを含む水性媒体に浸漬されて良い。別法として、一つ以上のポリマーを含む水性媒体を、生地にスプレーしても良い。 Polymer A or polymer B or both are mixed with an aqueous medium before being contacted with the dough. Alternatively, polymer A may be mixed with a non-aqueous medium containing a solvent such as alcohol and acetone before being contacted with the dough. However, it is preferred that the polymer or both polymers be mixed with an aqueous medium before contacting the dough. The dough may be immersed in an aqueous medium containing one or more polymers. Alternatively, an aqueous medium containing one or more polymers may be sprayed onto the dough.
ポリマーA及びBのいずれかは、処理される生地の表面に対して擦られて良いアブレイダブルスティックの形態で使用され、その後水性媒体と接触されても良いことも考慮される。 It is also contemplated that either polymer A and B may be used in the form of an abradable stick that may be rubbed against the surface of the fabric to be treated and then contacted with an aqueous medium.
組成物
本発明の第二の特徴点によれば、1から99重量%のポリマーA、1から99重量%のポリマーB、及び0から10重量%の酸性成分を含む生地の処理のための組成物が提供され、ここで
(a)ポリマーAはビニルアルコール、アルキレングリコール、サッカリド、及びカルボン酸のホモポリマーまたはコポリマーからなるクラスから選択され;及び
(b)ポリマーBはビニルピロリドン、アルキレンオキシド、サッカリド、及びカルボン酸のホモポリマーまたはコポリマーからなるクラスから選択され;
ポリマーA及びBは同じクラスのものではなく、前記組成物の1%水溶液のpHは6未満である。
Composition According to a second aspect of the present invention, a composition for the treatment of a dough comprising 1 to 99% by weight of polymer A, 1 to 99% by weight of polymer B, and 0 to 10% by weight of acidic components Wherein (a) polymer A is selected from the class consisting of homopolymers or copolymers of vinyl alcohol, alkylene glycol, saccharide, and carboxylic acid; and (b) polymer B is vinyl pyrrolidone, alkylene oxide, saccharide. And selected from the class consisting of homopolymers or copolymers of carboxylic acids;
Polymers A and B are not of the same class and the pH of a 1% aqueous solution of the composition is less than 6.
前記組成物は、好ましくは5から95重量%、より好ましくは10から90重量%、最も好ましくは20から80重量%のポリマーAを含む。前記組成物は、好ましくは5から95重量%、より好ましくは10から90重量%、最も好ましくは20から80重量%のポリマーBを含む。 Said composition preferably comprises 5 to 95% by weight of polymer A, more preferably 10 to 90% by weight, most preferably 20 to 80% by weight. Said composition preferably comprises 5 to 95%, more preferably 10 to 90%, most preferably 20 to 80% by weight of polymer B.
前記ポリマーは、前記組成物の1%水溶液のpHが6未満となるように選択されて良い。好ましくは、前記組成物の1%水溶液のpHが6未満となることを確保するために、前記組成物の0.1から10重量%で、前記組成物中に酸性成分が存在する。生成した水性媒体のpHを6未満に低下する酸性成分は当業者に周知であり、いずれかの適切な酸性成分が選択されて良い。 The polymer may be selected such that the pH of a 1% aqueous solution of the composition is less than 6. Preferably, acidic components are present in the composition at 0.1 to 10% by weight of the composition to ensure that the pH of a 1% aqueous solution of the composition is less than 6. Acidic components that lower the pH of the resulting aqueous medium to less than 6 are well known to those skilled in the art, and any suitable acidic component may be selected.
キット
本発明の第三の特徴点によれば、第二の特徴点の組成物と、使用のための一連の説明書とを含む生地の処理のためのキットが提供される。
Kit According to a third aspect of the present invention, there is provided a kit for treating a dough comprising a composition of the second aspect and a series of instructions for use.
ポリマーAとBとは別個の実装形態、即ちポリマーAとBとが別個の実装に個々に保持されているか、二つの区画の実装形態の別個の区画に保持されていることが特に好ましい。 It is particularly preferred that the polymers A and B are in separate implementations, i.e. the polymers A and B are individually held in separate implementations or are held in separate compartments in a two compartment implementation.
本発明は、ここで実施例で説明されるであろう。実施例は説明の目的のみを有するものであり、いずれの態様でも本発明の範囲を制限するものではない。 The invention will now be described by way of example. The examples are for illustrative purposes only and do not limit the scope of the invention in any way.
材料と方法
以下の材料が実施例で使用された:
Materials and Methods The following materials were used in the examples:
表2:実施例で使用される材料
沈着
ポリマーAは、実施例1及び2並びに比較例1−Aから2−Bでは、450000の分子量のポリアクリル酸であった。ポリマーBは、実施例1並びに比較例A及びBでは、90000の分子量のポリビニルピロリドンであった。実施例2並びに比較例C、D及び2AでのポリマーBは、100000の分子量のポリエチレンオキシドであった。
Deposition Polymer A was 450,000 molecular weight polyacrylic acid in Examples 1 and 2 and Comparative Examples 1-A to 2-B. Polymer B was 9 000 molecular weight polyvinyl pyrrolidone in Example 1 and Comparative Examples A and B. Polymer B in Example 2 and Comparative Examples C, D and 2A was a polyethylene oxide having a molecular weight of 100,000.
沈着の研究のために、約10gの生地を溶液中のポリマーで処理し、処理された生地の乾燥の後に重量測定により重量の増分を調べた。 For the deposition study, about 10 g of dough was treated with the polymer in solution and the weight increment was examined gravimetrically after drying of the treated dough.
表3:コットン、ポリコットン、及びポリエステル生地に対するポリマーの沈着
この結果から、本発明の方法によって一緒に使用された際の二種類のポリマーの沈着は、ポリマーの一方のみで処理された生地と比較して有意に高いことが観察できる。 From this result, it can be observed that the deposition of the two types of polymers when used together by the method of the present invention is significantly higher compared to a fabric treated with only one of the polymers.
汚れ
汚れのプロトコール
生地をポリマーで処理し乾かした。乾かした生地をナトリウムアルキルベンゼンスルホネート(50ppm)の添加によって安定化した水中の炭素スス分散物(150ppm)に浸漬した。生地を炭素スス溶液から取り出し、水中で迅速にすすいで乾かした。反射率の変化(ΔR)、即ち汚れ処理の前後での生地の反射率の差異は生地の汚れ具合の測定値であり、ΔRのマイナスの値は生地の汚れを示す。
Dirt protocol The fabric was treated with polymer and dried. The dried dough was immersed in a carbon soot dispersion (150 ppm) in water stabilized by the addition of sodium alkylbenzene sulfonate (50 ppm). The dough was removed from the carbon soot solution, rinsed quickly in water and dried. The change in reflectance (ΔR), that is, the difference in the reflectance of the fabric before and after the soiling treatment is a measured value of the soiling degree of the fabric, and a negative value of ΔR indicates the soiling of the fabric.
以下の表では、以下の略語を使用している:
PEG17500−分子量17500のポリエチレングリコール
PAA8000−分子量8000のポリエアクリル酸
PVA124000−分子量125000のポリビニルアルコール
PVP90000−分子量90000のポリビニルピロリドン。
The following abbreviations are used in the following table:
PEG 17500-Polyethylene glycol PAA 8000 with molecular weight 17500-Polyacrylic acid PVA 124000 with molecular weight 8000-Polyvinyl alcohol PVP 90000 with molecular weight 125000-Polyvinylpyrrolidone with molecular weight 90000
表4:炭素ススでのコットン生地の汚れ
この結果から、本発明の方法において処理された生地の汚れは、未処理の生地(比較例I)より有意に低く、一方のみのポリマーで処理した生地(比較例F、G及びH)に対しても有意に低い。 From this result, the soil of the fabric treated in the method of the present invention is significantly lower than that of untreated fabric (Comparative Example I), compared to fabric treated with only one polymer (Comparative Examples F, G and H). But it is significantly lower.
洗浄
洗浄プロトコール
生地をポリマーで処理し乾かした。乾かした生地をナトリウムアルキルベンゼンスルホネート(50ppm)の添加によって安定化した水中の炭素スス分散物(150ppm)に浸漬した。次いで生地を乾かした。乾かした生地を水、水中の炭酸ナトリウム溶液(0.15重量%)、及び水中の市販品の洗剤(SURF EXCEL(登録商標)0.3重量%)で洗浄した。反射率の変化(ΔR)は生地の洗浄の測定値であった。ΔRの値が大きいとより良好な洗浄を示す。
Washing and washing protocol The dough was treated with polymer and dried. The dried dough was immersed in a carbon soot dispersion (150 ppm) in water stabilized by the addition of sodium alkylbenzene sulfonate (50 ppm). The dough was then dried. The dried dough was washed with water, sodium carbonate solution in water (0.15% by weight), and a commercial detergent in water (SURF EXCEL® 0.3% by weight). The change in reflectance (ΔR) was a measure of the fabric wash. Larger values of ΔR indicate better cleaning.
ポリマーAは分子量2000のポリアクリル酸であり、ポリマーBは分子量90000のポリビニルピロリドンであった。実施例6では、0.2重量%の水性媒体で両者のポリマーを使用した。水性媒体のpHは3.0であった。比較例J及びKでは、ポリマーAとBをそれぞれ単独で使用し、それぞれ水性媒体の0.4重量%であった(それぞれpH2.7及び7.0)。比較例Lは未処理の生地である(pH7)。生地(コットン、ポリコットン及びポリエステル)を、所定のプロトコールに従って洗浄し、その結果が以下に要約されている。 The polymer A was polyacrylic acid having a molecular weight of 2000, and the polymer B was polyvinylpyrrolidone having a molecular weight of 90000. In Example 6, both polymers were used in a 0.2 wt% aqueous medium. The pH of the aqueous medium was 3.0. In Comparative Examples J and K, Polymers A and B were each used alone, each at 0.4% by weight of the aqueous medium (pH 2.7 and 7.0, respectively). Comparative Example L is an untreated dough (pH 7). The fabrics (cotton, polycotton and polyester) are washed according to a predetermined protocol and the results are summarized below.
表5:炭素ススで汚された生地の洗浄
この結果から、本発明の範囲内にある実施例6についての洗浄効率は、本発明の範囲外である比較例J、K及びLで得られた洗浄効率より高い。特に、炭酸ナトリウムまたは水で洗浄した場合に洗浄効率はより良好である。更にこの結果は、市販品の洗剤で洗浄した際に、ポリコットン及びポリエステルで特に洗浄効率が増大することを示す。 From this result, the cleaning efficiency for Example 6 within the scope of the present invention is higher than the cleaning efficiency obtained with Comparative Examples J, K and L which are outside the scope of the present invention. In particular, the washing efficiency is better when washed with sodium carbonate or water. Furthermore, the results show that the cleaning efficiency increases especially with polycotton and polyester when washed with a commercial detergent.
電解質の効果
ポリマーAは分子量450000のポリアクリル酸であり、ポリマーBは分子量1300000のポリビニルピロリドンであった。全ての実施例では、両者のポリマーを水性媒体の0.1重量%で使用した。電解質添加の効果を、全水性媒体の0.1重量%での各種の電解質を添加することにより調べた。水性媒体のpHは、2.7から3.0の範囲であった。生地(コットン、ポリコットン及びポリエステル)を、水中の炭酸ナトリウム(0.15重量%)を使用して洗浄した。その結果が、洗浄効率の観点で以下に要約されている。
Effect of Electrolyte Polymer A was polyacrylic acid having a molecular weight of 450,000, and polymer B was polyvinylpyrrolidone having a molecular weight of 1300000. In all examples, both polymers were used at 0.1% by weight of the aqueous medium. The effect of electrolyte addition was investigated by adding various electrolytes at 0.1% by weight of the total aqueous medium. The pH of the aqueous medium was in the range of 2.7 to 3.0. The dough (cotton, polycotton and polyester) was washed using sodium carbonate (0.15 wt%) in water. The results are summarized below in terms of cleaning efficiency.
表6:電解質の添加の効果
この結果から、電解質の添加は、特にポリコットン及びポリエステル生地について、洗浄効率のさらなる増大を導くことが明らかである。更に、コットン生地については、塩化カルシウムが特に洗浄効率の増大を与える。 From this result, it is clear that the addition of electrolyte leads to a further increase in cleaning efficiency, especially for polycotton and polyester fabrics. Furthermore, for cotton fabrics, calcium chloride particularly increases cleaning efficiency.
香料沈着
プロトコール
アリルアミルグリコレートを代表的な香料成分として用いた。ポリマーAは分子量450000を有するポリアクリル酸であり、ポリマーBは分子量90000を有するポリビニルピロリドンであった。水性媒体にそれぞれ0.1重量%でポリマーAとBの両者を有する実施例11−pH2.8、水性媒体にそれぞれ0.2重量%でポリマーAとポリマーBをそれぞれ単独で有するそれぞれ比較例M−pH3及び比較例N−pH7、並びに未処理の生地として比較例O−pH7に対して香料を添加した。生地を臭気分析器により香料の保持について試験し、0〜5(0のスコアは臭気強度がないことを示し、5のスコアは最大の臭気強度を示す)のスケールで記録した。詳細は以下の表に要約される。
Perfume Deposition Protocol Allyl amyl glycolate was used as a representative perfume ingredient. Polymer A was polyacrylic acid having a molecular weight of 450,000, and polymer B was polyvinylpyrrolidone having a molecular weight of 90000. Example 11 having both polymer A and B at 0.1% by weight in aqueous medium-pH 2.8, respectively Comparative Example M having polymer A and polymer B alone at 0.2% by weight in aqueous medium, respectively -Perfume was added to pH 3 and Comparative Example N-pH 7, and Comparative Example O-pH 7 as an untreated dough. The dough was tested for fragrance retention with an odor analyzer and recorded on a scale of 0 to 5 (a score of 0 indicates no odor intensity and a score of 5 indicates maximum odor intensity). Details are summarized in the following table.
表7:生地に対する香料の沈着
上記の表の結果から、60分での香料強度は、本発明の方法によって処理された生地について有意に高い。 From the results in the above table, the perfume intensity at 60 minutes is significantly higher for the dough treated by the method of the present invention.
蛍光沈着
以下の実験を、蛍光剤として2ppmのCBSX(CIBA;登録商標)を使用して実施した。ポリマーAとBの詳細は以下に要約され、併せてコットンでの反射率の値によって測定された白色スコアに関する結果が示されている。
Fluorescence deposition The following experiments were performed using 2 ppm CBSX (CIBA) as the fluorescent agent. Details of polymers A and B are summarized below, together with the results for the white score measured by the reflectance value on cotton.
表8:生地に対する蛍光の沈着
この結果から、白色スコアによって示される蛍光沈着は、未処理の生地(比較例R)または一方のみのポリマーで処理された生地(比較例P及びQ)と比較して、本発明の方法によるポリマーAとBの両者で処理された生地(実施例12)で増大することが明らかである。 From this result, the fluorescence deposition indicated by the white score is higher than that of the untreated fabric (Comparative Example R) or the fabric treated with only one polymer (Comparative Examples P and Q). It is evident that the dough (Example 12) treated with both A and B increases.
上記実施例は、本発明の方法を実施できる態様を明確且つ十分に記載していると理解されるであろう。更に、本発明の方法は、生地の汚れを減少し、後の洗浄の効率を改善し、有益な試薬の沈着の増大を可能にし、コットン、ポリコットン及びポリエステルを含む各種のタイプの生地で有効である生地の処理方法を提供する目的に適合できることが理解されるであろう。 It will be understood that the above examples clearly and fully describe the manner in which the method of the present invention can be practiced. In addition, the method of the present invention reduces fabric soiling, improves the efficiency of subsequent cleaning, allows for increased deposition of beneficial reagents, and is effective on various types of fabrics including cotton, polycotton and polyester. It will be understood that it can be adapted to the purpose of providing a method of treating a dough.
Claims (11)
(a)ポリマーAはビニルアルコール、アルキレングリコール、サッカリド、及びカルボン酸のホモポリマーまたはコポリマーからなるクラスから選択され;及び
(b)ポリマーBはビニルピロリドン、アルキレンオキシド、サッカリド、及びカルボン酸のホモポリマーまたはコポリマーからなるクラスから選択され;
ポリマーA及びBは同じクラスのものではなく、水性媒体は6未満のpHを有する、方法。 A method for treating a dough comprising the step of contacting the dough with polymers A and B in an aqueous medium,
(A) Polymer A is selected from the class consisting of homopolymers or copolymers of vinyl alcohol, alkylene glycols, saccharides, and carboxylic acids; and (b) Polymer B is a homopolymer of vinyl pyrrolidone, alkylene oxides, saccharides, and carboxylic acids. Or selected from the class consisting of copolymers;
Polymers A and B are not of the same class and the aqueous medium has a pH of less than 6.
(a)ポリマーAはビニルアルコール、アルキレングリコール、サッカリド、及びカルボン酸のホモポリマーまたはコポリマーからなるクラスから選択され;及び
(b)ポリマーBはビニルピロリドン、アルキレンオキシド、サッカリド、及びカルボン酸のホモポリマーまたはコポリマーからなるクラスから選択され;
ポリマーA及びBは同じクラスのものではなく、前記組成物の1%水溶液のpHは6未満である、組成物。 A composition for the treatment of a dough comprising 1 to 99% by weight of polymer A, 1 to 99% by weight of polymer B, and 0 to 10% by weight of an acidic component,
(A) Polymer A is selected from the class consisting of homopolymers or copolymers of vinyl alcohol, alkylene glycols, saccharides, and carboxylic acids; and (b) Polymer B is a homopolymer of vinyl pyrrolidone, alkylene oxides, saccharides, and carboxylic acids. Or selected from the class consisting of copolymers;
Polymers A and B are not of the same class and the pH of a 1% aqueous solution of the composition is less than 6.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN2459/MUM/2007 | 2007-12-14 | ||
IN2459MU2007 | 2007-12-14 | ||
EP08150762 | 2008-01-29 | ||
EP08150762.6 | 2008-01-29 | ||
PCT/EP2008/064764 WO2009077255A1 (en) | 2007-12-14 | 2008-10-31 | Process for treatment of a fabric |
Publications (2)
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JP2011506788A true JP2011506788A (en) | 2011-03-03 |
JP5080652B2 JP5080652B2 (en) | 2012-11-21 |
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JP2010537346A Expired - Fee Related JP5080652B2 (en) | 2007-12-14 | 2008-10-31 | How to treat the dough |
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US (1) | US20100297359A1 (en) |
EP (1) | EP2220288B1 (en) |
JP (1) | JP5080652B2 (en) |
CN (1) | CN101889111B (en) |
AT (1) | ATE544901T1 (en) |
AU (1) | AU2008337741B2 (en) |
BR (1) | BRPI0820909B1 (en) |
CA (1) | CA2707805C (en) |
MY (1) | MY153922A (en) |
RU (1) | RU2473724C2 (en) |
WO (1) | WO2009077255A1 (en) |
ZA (1) | ZA201002991B (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
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AU2010291393B2 (en) * | 2009-09-02 | 2013-07-11 | Unilever Plc | Composition and process for treatment of a fabric |
WO2013113541A1 (en) | 2012-01-31 | 2013-08-08 | Unilever N.V. | A composition and method for treating substrates |
CN111032791A (en) * | 2017-09-21 | 2020-04-17 | 捷德货币技术有限责任公司 | Method for producing pigment chips having a predetermined inner and/or outer contour using a crack-forming layer, and pigment chips |
EP4108752A1 (en) * | 2021-06-25 | 2022-12-28 | The Procter & Gamble Company | Detergent compositions |
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- 2008-10-31 MY MYPI2010002715A patent/MY153922A/en unknown
- 2008-10-31 BR BRPI0820909-0A patent/BRPI0820909B1/en not_active IP Right Cessation
- 2008-10-31 US US12/747,217 patent/US20100297359A1/en not_active Abandoned
- 2008-10-31 CN CN2008801197927A patent/CN101889111B/en not_active Expired - Fee Related
- 2008-10-31 JP JP2010537346A patent/JP5080652B2/en not_active Expired - Fee Related
- 2008-10-31 RU RU2010129064/05A patent/RU2473724C2/en not_active IP Right Cessation
- 2008-10-31 CA CA2707805A patent/CA2707805C/en not_active Expired - Fee Related
- 2008-10-31 AU AU2008337741A patent/AU2008337741B2/en not_active Ceased
- 2008-10-31 AT AT08861303T patent/ATE544901T1/en active
- 2008-10-31 EP EP08861303A patent/EP2220288B1/en not_active Not-in-force
- 2008-10-31 WO PCT/EP2008/064764 patent/WO2009077255A1/en active Application Filing
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2010
- 2010-04-29 ZA ZA2010/02991A patent/ZA201002991B/en unknown
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JPS5421405A (en) * | 1977-07-19 | 1979-02-17 | Lion Corp | Detergent composition |
JPS57126898A (en) * | 1980-12-17 | 1982-08-06 | Unilever Nv | Detergent composition |
JPS6337200A (en) * | 1986-07-30 | 1988-02-17 | ユニリ−バ−・ナ−ムロ−ゼ・ベンノ−トシヤ−プ | Detergent composition |
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Also Published As
Publication number | Publication date |
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JP5080652B2 (en) | 2012-11-21 |
AU2008337741B2 (en) | 2011-11-24 |
ZA201002991B (en) | 2011-07-27 |
RU2010129064A (en) | 2012-01-20 |
BRPI0820909B1 (en) | 2018-02-27 |
WO2009077255A1 (en) | 2009-06-25 |
CN101889111B (en) | 2013-01-23 |
EP2220288A1 (en) | 2010-08-25 |
CA2707805C (en) | 2016-10-11 |
CA2707805A1 (en) | 2009-06-25 |
ATE544901T1 (en) | 2012-02-15 |
BRPI0820909A2 (en) | 2015-07-28 |
RU2473724C2 (en) | 2013-01-27 |
US20100297359A1 (en) | 2010-11-25 |
AU2008337741A1 (en) | 2009-06-25 |
MY153922A (en) | 2015-04-15 |
CN101889111A (en) | 2010-11-17 |
EP2220288B1 (en) | 2012-02-08 |
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