RU2008132440A - Способ получения водной дисперсии полиуретана, пригодной для использования в продуктах личной гигиены, фиксаторе для волос и лосьоне для загара на основе указанной дисперсии - Google Patents
Способ получения водной дисперсии полиуретана, пригодной для использования в продуктах личной гигиены, фиксаторе для волос и лосьоне для загара на основе указанной дисперсии Download PDFInfo
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- RU2008132440A RU2008132440A RU2008132440/04A RU2008132440A RU2008132440A RU 2008132440 A RU2008132440 A RU 2008132440A RU 2008132440/04 A RU2008132440/04 A RU 2008132440/04A RU 2008132440 A RU2008132440 A RU 2008132440A RU 2008132440 A RU2008132440 A RU 2008132440A
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- Prior art keywords
- radical
- polyurethane
- molecular weight
- diol
- dispersion
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- 239000004814 polyurethane Substances 0.000 title claims abstract 13
- 229920002635 polyurethane Polymers 0.000 title claims abstract 13
- 239000006185 dispersion Substances 0.000 title claims abstract 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims abstract 4
- 239000006210 lotion Substances 0.000 title claims 2
- 238000004519 manufacturing process Methods 0.000 title 1
- 238000000034 method Methods 0.000 claims abstract 15
- 125000003010 ionic group Chemical group 0.000 claims abstract 8
- 150000002009 diols Chemical class 0.000 claims abstract 7
- 229920000233 poly(alkylene oxides) Polymers 0.000 claims abstract 5
- 239000005056 polyisocyanate Substances 0.000 claims abstract 5
- 229920001228 polyisocyanate Polymers 0.000 claims abstract 5
- 239000004970 Chain extender Substances 0.000 claims abstract 4
- 125000001931 aliphatic group Chemical group 0.000 claims abstract 4
- 125000002947 alkylene group Chemical group 0.000 claims abstract 4
- 239000003960 organic solvent Substances 0.000 claims abstract 4
- 239000004417 polycarbonate Substances 0.000 claims abstract 4
- 229920000515 polycarbonate Polymers 0.000 claims abstract 4
- 229920005862 polyol Polymers 0.000 claims abstract 4
- 150000003077 polyols Chemical class 0.000 claims abstract 4
- 125000000524 functional group Chemical group 0.000 claims abstract 3
- 230000003993 interaction Effects 0.000 claims abstract 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims 5
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 3
- 150000001875 compounds Chemical class 0.000 claims 3
- 239000000203 mixture Substances 0.000 claims 3
- PTBDIHRZYDMNKB-UHFFFAOYSA-N 2,2-Bis(hydroxymethyl)propionic acid Chemical compound OCC(C)(CO)C(O)=O PTBDIHRZYDMNKB-UHFFFAOYSA-N 0.000 claims 2
- JVYDLYGCSIHCMR-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)butanoic acid Chemical compound CCC(CO)(CO)C(O)=O JVYDLYGCSIHCMR-UHFFFAOYSA-N 0.000 claims 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 claims 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 claims 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 claims 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims 2
- -1 amido amines Chemical class 0.000 claims 2
- 150000001412 amines Chemical class 0.000 claims 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 claims 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 claims 2
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 claims 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 claims 2
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 claims 2
- PLFFHJWXOGYWPR-HEDMGYOXSA-N (4r)-4-[(3r,3as,5ar,5br,7as,11as,11br,13ar,13bs)-5a,5b,8,8,11a,13b-hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-3-yl]pentan-1-ol Chemical compound C([C@]1(C)[C@H]2CC[C@H]34)CCC(C)(C)[C@@H]1CC[C@@]2(C)[C@]4(C)CC[C@@H]1[C@]3(C)CC[C@@H]1[C@@H](CCCO)C PLFFHJWXOGYWPR-HEDMGYOXSA-N 0.000 claims 1
- GFNDFCFPJQPVQL-UHFFFAOYSA-N 1,12-diisocyanatododecane Chemical compound O=C=NCCCCCCCCCCCCN=C=O GFNDFCFPJQPVQL-UHFFFAOYSA-N 0.000 claims 1
- OVBFMUAFNIIQAL-UHFFFAOYSA-N 1,4-diisocyanatobutane Chemical compound O=C=NCCCCN=C=O OVBFMUAFNIIQAL-UHFFFAOYSA-N 0.000 claims 1
- CDMDQYCEEKCBGR-UHFFFAOYSA-N 1,4-diisocyanatocyclohexane Chemical compound O=C=NC1CCC(N=C=O)CC1 CDMDQYCEEKCBGR-UHFFFAOYSA-N 0.000 claims 1
- 229940008841 1,6-hexamethylene diisocyanate Drugs 0.000 claims 1
- IVGRSQBDVIJNDA-UHFFFAOYSA-N 2-(2-aminoethylamino)ethanesulfonic acid Chemical compound NCCNCCS(O)(=O)=O IVGRSQBDVIJNDA-UHFFFAOYSA-N 0.000 claims 1
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 claims 1
- UDZFEGOYTOHDHK-UHFFFAOYSA-N 3-ethyl-1-N-methylpentane-1,3-diamine Chemical compound CCC(N)(CC)CCNC UDZFEGOYTOHDHK-UHFFFAOYSA-N 0.000 claims 1
- CDBAMNGURPMUTG-UHFFFAOYSA-N 4-[2-(4-hydroxycyclohexyl)propan-2-yl]cyclohexan-1-ol Chemical compound C1CC(O)CCC1C(C)(C)C1CCC(O)CC1 CDBAMNGURPMUTG-UHFFFAOYSA-N 0.000 claims 1
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 claims 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims 1
- 239000004146 Propane-1,2-diol Substances 0.000 claims 1
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 claims 1
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 claims 1
- 150000001735 carboxylic acids Chemical class 0.000 claims 1
- PDXRQENMIVHKPI-UHFFFAOYSA-N cyclohexane-1,1-diol Chemical compound OC1(O)CCCCC1 PDXRQENMIVHKPI-UHFFFAOYSA-N 0.000 claims 1
- KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 claims 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 claims 1
- WEHWNAOGRSTTBQ-UHFFFAOYSA-N dipropylamine Chemical compound CCCNCCC WEHWNAOGRSTTBQ-UHFFFAOYSA-N 0.000 claims 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 claims 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 claims 1
- QHJABUZHRJTCAR-UHFFFAOYSA-N n'-methylpropane-1,3-diamine Chemical compound CNCCCN QHJABUZHRJTCAR-UHFFFAOYSA-N 0.000 claims 1
- DUUJJGXCSXGCBK-UHFFFAOYSA-N n-(7-methyloctoxy)propan-1-amine Chemical compound CCCNOCCCCCCC(C)C DUUJJGXCSXGCBK-UHFFFAOYSA-N 0.000 claims 1
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 claims 1
- 150000003141 primary amines Chemical class 0.000 claims 1
- 229960004063 propylene glycol Drugs 0.000 claims 1
- 235000013772 propylene glycol Nutrition 0.000 claims 1
- 159000000000 sodium salts Chemical group 0.000 claims 1
- 150000003512 tertiary amines Chemical class 0.000 claims 1
- 229920003009 polyurethane dispersion Polymers 0.000 abstract 1
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
- C08J3/03—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media
- C08J3/07—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media from polymer solutions
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
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- C08G18/12—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step using two or more compounds having active hydrogen in the first polymerisation step
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/87—Polyurethanes
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
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- A61Q5/00—Preparations for care of the hair
- A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- C08G18/0819—Manufacture of polymers containing ionic or ionogenic groups containing anionic or anionogenic groups
- C08G18/0823—Manufacture of polymers containing ionic or ionogenic groups containing anionic or anionogenic groups containing carboxylate salt groups or groups forming them
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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- C08G18/0838—Manufacture of polymers in the presence of non-reactive compounds
- C08G18/0842—Manufacture of polymers in the presence of non-reactive compounds in the presence of liquid diluents
- C08G18/0861—Manufacture of polymers in the presence of non-reactive compounds in the presence of liquid diluents in the presence of a dispersing phase for the polymers or a phase dispersed in the polymers
- C08G18/0866—Manufacture of polymers in the presence of non-reactive compounds in the presence of liquid diluents in the presence of a dispersing phase for the polymers or a phase dispersed in the polymers the dispersing or dispersed phase being an aqueous medium
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/2805—Compounds having only one group containing active hydrogen
- C08G18/2815—Monohydroxy compounds
- C08G18/283—Compounds containing ether groups, e.g. oxyalkylated monohydroxy compounds
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/4009—Two or more macromolecular compounds not provided for in one single group of groups C08G18/42 - C08G18/64
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
- C08G18/44—Polycarbonates
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/4825—Polyethers containing two hydroxy groups
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
- C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
- C08G18/6633—Compounds of group C08G18/42
- C08G18/6637—Compounds of group C08G18/42 with compounds of group C08G18/32 or polyamines of C08G18/38
- C08G18/664—Compounds of group C08G18/42 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3203
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
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- C08G18/6633—Compounds of group C08G18/42
- C08G18/6659—Compounds of group C08G18/42 with compounds of group C08G18/34
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- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/721—Two or more polyisocyanates not provided for in one single group C08G18/73 - C08G18/80
- C08G18/722—Combination of two or more aliphatic and/or cycloaliphatic polyisocyanates
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- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes
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- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Dispersion Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Manufacturing & Machinery (AREA)
- Engineering & Computer Science (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
- Polyurethanes Or Polyureas (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
1. Способ получения водной дисперсии полиуретана, пригодной для использования в предметах личной гигиены, содержащий: ! 1) получение форполимера по формуле: ! ! где R1 представляет собой двухвалентный радикал поликарбонатполиола, ! R2 представляет собой радикал алифатического или циклоалифатического полиизоцианата, ! R3 представляет собой радикал низкомолекулярного диола, возможно, замещенного ионными группами, ! n составляет от 1 до 5, и ! m составляет >1; ! путем взаимодействия: ! 1а) по меньшей мере, одного поликарбонатполиола, ! 1б) одного или нескольких алифатических или циклоалифатических полиизоцианатов, и ! 1в) по меньшей мере, одного низкомолекулярного диола, возможно, замещенного ионными группами; ! 2) реакцию этого форполимера с, по меньшей мере, одним полиалкиленоксидом с моногидроксильными функциональными группами со среднечисловой молекулярной массой, равной или менее около 3000; ! 3) удлинение цепи этого форполимера реакцией с ! 3а) по меньшей мере, одним удлинителем цепи формулы: ! H2N-R4-NH2 ! где R4 представляет собой радикал алкилена или алкиленоксида, не замещенный ионными или потенциально ионными группами, и ! 3б) обязательно, по меньшей мере, одним удлинителем цепи формулы: ! H2N-R5-NH2 ! где R5 представляет собой радикал алкилена, замещенный ионными или потенциально ионными группами, ! в присутствии органического растворителя, чтобы сформировать полиуретан; ! 4) диспергирование полиуретана в воде; и ! 5) удаление органического растворителя, получая водную дисперсию полиуретана; где радикал полиалкиленоксида с моногидроксильными функциональными группами составляет между около 0,1% по весу и около 5% по весу полиуретана. ! 2. С�
Claims (14)
1. Способ получения водной дисперсии полиуретана, пригодной для использования в предметах личной гигиены, содержащий:
1) получение форполимера по формуле:
где R1 представляет собой двухвалентный радикал поликарбонатполиола,
R2 представляет собой радикал алифатического или циклоалифатического полиизоцианата,
R3 представляет собой радикал низкомолекулярного диола, возможно, замещенного ионными группами,
n составляет от 1 до 5, и
m составляет >1;
путем взаимодействия:
1а) по меньшей мере, одного поликарбонатполиола,
1б) одного или нескольких алифатических или циклоалифатических полиизоцианатов, и
1в) по меньшей мере, одного низкомолекулярного диола, возможно, замещенного ионными группами;
2) реакцию этого форполимера с, по меньшей мере, одним полиалкиленоксидом с моногидроксильными функциональными группами со среднечисловой молекулярной массой, равной или менее около 3000;
3) удлинение цепи этого форполимера реакцией с
3а) по меньшей мере, одним удлинителем цепи формулы:
H2N-R4-NH2
где R4 представляет собой радикал алкилена или алкиленоксида, не замещенный ионными или потенциально ионными группами, и
3б) обязательно, по меньшей мере, одним удлинителем цепи формулы:
H2N-R5-NH2
где R5 представляет собой радикал алкилена, замещенный ионными или потенциально ионными группами,
в присутствии органического растворителя, чтобы сформировать полиуретан;
4) диспергирование полиуретана в воде; и
5) удаление органического растворителя, получая водную дисперсию полиуретана; где радикал полиалкиленоксида с моногидроксильными функциональными группами составляет между около 0,1% по весу и около 5% по весу полиуретана.
2. Способ по п.1, где этот способ далее содержит обрыв цепи форполимера, по меньшей мере, одним соединением формулы:
где R6 представляет собой атом Н или радикал алкилена, необязательно, имеющий гидроксильный конец, a R7 представляет собой радикал алкилена, необязательно, имеющий гидроксильный конец.
3. Способ по п.2, где соединение, обрывающее цепи, выбрано из группы, состоящей из метиламина, этиламина, пропиламина, бутиламина, октиламина, лауриламина, стеариламина, изононилокси-пропиламина, диметиламина, диэтиламина, дипропиламина, дибутиламина, N-метиламинопропиламина, диэтил(метил)аминопропиламина, морфолина, пиперидина и диэтаноламина, амидоаминов двупервичных аминов и одноосновных карбоновых кислот, монокетиминов двупервичных аминов, первичных/третичных аминов, метанола, бутанола, гексанола, 2-этилгексилового спирта, изодецилового спирта, аминометилпропанола и их смесей.
4. Способ по п.1, где один или несколько полиизоцианатов выбрано из группы, состоящей из тетраметилендиизоцианата, 1,6-гексаметилендиизоцианата, додекаметилендиизоцианата, 1,4-диизоцианатоциклогексана, 3-изоцианатометил-3,5,5-триметилциклогексилизоцианата (изофорондиизоцианата), 4,4′-диизоцианатодициклогексилметана, 4,4′-диизоцианатодициклогексилпропана-(2,2) и их смесей.
5. Способ по п.1, где низкомолекулярный диол выбран из группы, состоящей из этиленгликоля, диэтиленгликоля, пропан-1,2-диола, пропан-1,3-диола, бутан-1,4-диола, бутилен-1,3-гликоля, циклогександиола, 1,4-циклогександиметанола, гексан-1,6-диола, бисфенола А (2,2-бис(4-гидроксифенил)пропана), гидрированного бисфенола А (2,2-бис(4-гидроксициклогексил)пропана) и их смесей.
6. Способ по п.1, где низкомолекулярный диол выбран из группы, состоящей из диметилолбутановой кислоты и диметилолпропановой кислоты.
7. Способ по п.3, где низкомолекулярный диол выбран из группы, состоящей из диметилолбутановой кислоты и диметилолпропановой кислоты.
8. Способ по п.1, где второй удлинитель цепи представляет собой натриевую соль N-(2-аминоэтил)-2-аминоэтансульфокислоты.
9. Способ по п.1, где соединение полиалкиленоксида с моногидроксильными функциональными группами представляет собой моноол полиэтиленоксида, имеющий среднечисловую молекулярную массу, приблизительно, 2220.
10. Способ по п.1, где n составляет от 1 до 3, а m составляет от 1 до 5.
11. Способ по п.1, где либо R3 представляет собой радикал диэтиленгликоля, либо R4 представляет собой радикал дипропиламин-диэтиленгликоля.
12. Фиксатор для волос, содержащий водную дисперсию полиуретана, полученную способом по п.1, и воду.
13. Фиксатор для волос, содержащий водную дисперсию полиуретана по п.12 и этанол.
14. Лосьон для загара, содержащий водную дисперсию полиуретана, полученную способом по п.1.
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US11/890,979 US7452525B1 (en) | 2007-08-08 | 2007-08-08 | Polyurethane dispersions based on polycarbonate polyols and suitable for use in personal care products |
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EP2028205B1 (en) | 2012-06-20 |
CN101361701B (zh) | 2013-04-24 |
RU2487900C2 (ru) | 2013-07-20 |
US20090041689A1 (en) | 2009-02-12 |
CA2637869A1 (en) | 2009-02-08 |
JP5410049B2 (ja) | 2014-02-05 |
JP2009046673A (ja) | 2009-03-05 |
KR20090015842A (ko) | 2009-02-12 |
TW200914058A (en) | 2009-04-01 |
BRPI0803505A2 (pt) | 2009-05-12 |
KR101545348B1 (ko) | 2015-08-18 |
CN101361701A (zh) | 2009-02-11 |
US8034322B2 (en) | 2011-10-11 |
TWI468181B (zh) | 2015-01-11 |
US7452525B1 (en) | 2008-11-18 |
EP2028205A1 (en) | 2009-02-25 |
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