AU783970B2 - Method for manufacturing amphoteric urethane resin and amphoteric urethane resin and resin composition obtained herewith - Google Patents
Method for manufacturing amphoteric urethane resin and amphoteric urethane resin and resin composition obtained herewith Download PDFInfo
- Publication number
- AU783970B2 AU783970B2 AU50677/02A AU5067702A AU783970B2 AU 783970 B2 AU783970 B2 AU 783970B2 AU 50677/02 A AU50677/02 A AU 50677/02A AU 5067702 A AU5067702 A AU 5067702A AU 783970 B2 AU783970 B2 AU 783970B2
- Authority
- AU
- Australia
- Prior art keywords
- compound
- urethane resin
- amino group
- manufacturing
- amphoteric urethane
- 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.)
- Ceased
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- 229920002803 thermoplastic polyurethane Polymers 0.000 title claims description 175
- 238000004519 manufacturing process Methods 0.000 title claims description 95
- 238000000034 method Methods 0.000 title claims description 45
- 239000011342 resin composition Substances 0.000 title claims description 14
- 150000001875 compounds Chemical class 0.000 claims description 192
- -1 polyol compound Chemical class 0.000 claims description 72
- 229920001296 polysiloxane Polymers 0.000 claims description 70
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 47
- 239000007864 aqueous solution Substances 0.000 claims description 45
- 238000006243 chemical reaction Methods 0.000 claims description 33
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 30
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 26
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 25
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 claims description 22
- 229920005862 polyol Polymers 0.000 claims description 19
- 239000000126 substance Substances 0.000 claims description 17
- 239000007795 chemical reaction product Substances 0.000 claims description 14
- 238000002156 mixing Methods 0.000 claims description 13
- 125000001302 tertiary amino group Chemical group 0.000 claims description 13
- 239000004205 dimethyl polysiloxane Substances 0.000 claims description 9
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims description 9
- 229920001577 copolymer Polymers 0.000 claims description 8
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 7
- 229920001400 block copolymer Polymers 0.000 claims description 5
- 125000004122 cyclic group Chemical group 0.000 claims description 5
- 239000005056 polyisocyanate Substances 0.000 claims description 5
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- 229920005604 random copolymer Polymers 0.000 claims description 4
- 229920002472 Starch Polymers 0.000 claims description 3
- 125000003277 amino group Chemical group 0.000 claims description 3
- 239000008107 starch Substances 0.000 claims description 3
- 235000019698 starch Nutrition 0.000 claims description 3
- 239000000834 fixative Substances 0.000 description 70
- 230000000052 comparative effect Effects 0.000 description 52
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 30
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- 239000011347 resin Substances 0.000 description 27
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- 229910052799 carbon Inorganic materials 0.000 description 18
- 238000011156 evaluation Methods 0.000 description 18
- 239000007921 spray Substances 0.000 description 17
- 238000005406 washing Methods 0.000 description 16
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 15
- 150000002430 hydrocarbons Chemical group 0.000 description 14
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- 239000004721 Polyphenylene oxide Substances 0.000 description 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
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- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 3
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- 229910052710 silicon Inorganic materials 0.000 description 3
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- WADSJYLPJPTMLN-UHFFFAOYSA-N 3-(cycloundecen-1-yl)-1,2-diazacycloundec-2-ene Chemical compound C1CCCCCCCCC=C1C1=NNCCCCCCCC1 WADSJYLPJPTMLN-UHFFFAOYSA-N 0.000 description 2
- CDOUZKKFHVEKRI-UHFFFAOYSA-N 3-bromo-n-[(prop-2-enoylamino)methyl]propanamide Chemical compound BrCCC(=O)NCNC(=O)C=C CDOUZKKFHVEKRI-UHFFFAOYSA-N 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
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- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
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- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 2
- 238000012644 addition polymerization Methods 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 230000002421 anti-septic effect Effects 0.000 description 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 description 2
- 235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 2
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- 235000011187 glycerol Nutrition 0.000 description 2
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
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- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 150000002500 ions Chemical group 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
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- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
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- 239000002453 shampoo Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- ZNVGYHOBTCWGTO-UHFFFAOYSA-N solutin Natural products Cc1cc(O)cc2OC(C)(O)C(=O)c12 ZNVGYHOBTCWGTO-UHFFFAOYSA-N 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000012970 tertiary amine catalyst Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 150000004072 triols Chemical class 0.000 description 1
Classifications
-
- 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
- C08G18/6659—Compounds of group C08G18/42 with compounds of group C08G18/34
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—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
- A61K8/89—Polysiloxanes
- A61K8/896—Polysiloxanes containing atoms other than silicon, carbon, oxygen and hydrogen, e.g. dimethicone copolyol phosphate
- A61K8/898—Polysiloxanes containing atoms other than silicon, carbon, oxygen and hydrogen, e.g. dimethicone copolyol phosphate containing nitrogen, e.g. amodimethicone, trimethyl silyl amodimethicone or dimethicone propyl PG-betaine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
-
- 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
- C08G18/08—Processes
- C08G18/0804—Manufacture of polymers containing ionic or ionogenic groups
- 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
-
- 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
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
- 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
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Polyurethanes Or Polyureas (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Cosmetics (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001194685A JP4688351B2 (ja) | 2001-06-27 | 2001-06-27 | 両性ウレタン樹脂の製造方法、その製造方法で得られる両性ウレタン樹脂及び樹脂組成物 |
| JP2001-194685 | 2001-06-27 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU5067702A AU5067702A (en) | 2003-01-02 |
| AU783970B2 true AU783970B2 (en) | 2006-01-12 |
Family
ID=19032776
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU50677/02A Ceased AU783970B2 (en) | 2001-06-27 | 2002-06-27 | Method for manufacturing amphoteric urethane resin and amphoteric urethane resin and resin composition obtained herewith |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US6646092B2 (enExample) |
| EP (1) | EP1275672B1 (enExample) |
| JP (1) | JP4688351B2 (enExample) |
| CN (1) | CN1260263C (enExample) |
| AU (1) | AU783970B2 (enExample) |
| BR (1) | BR0203347A (enExample) |
| DE (1) | DE60207154T2 (enExample) |
| MX (1) | MXPA02006419A (enExample) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1303124C (zh) * | 2004-01-30 | 2007-03-07 | 香港理工大学 | 水基嵌段聚氨酯、其制法及由其制备的防水、保暖、透湿性材料 |
| US20070185003A1 (en) * | 2006-01-18 | 2007-08-09 | Invista North America S.A.R.L. | Non-textile polymer compositions and methods |
| JP5463612B2 (ja) * | 2006-09-28 | 2014-04-09 | 横浜ゴム株式会社 | ウレタンエマルジョン |
| JP4450427B2 (ja) * | 2007-11-13 | 2010-04-14 | 株式会社資生堂 | 皮膚化粧料 |
| DE102008006004B3 (de) * | 2008-01-25 | 2009-08-27 | Bayer Materialscience Ag | Thermoplastische Polyurethane und deren Verwendung |
| CN101225150B (zh) * | 2008-01-28 | 2010-06-09 | 浙江大学 | 水分散有机硅-聚氨酯嵌段共聚物的合成方法及应用 |
| CN101225226B (zh) * | 2008-01-28 | 2010-11-24 | 浙江大学 | 水分散蒙脱土/有机硅嵌段聚氨酯纳米复合材料的制备方法及用途 |
| EP2113546A1 (en) | 2008-04-28 | 2009-11-04 | Schlumberger Holdings Limited | Swellable compositions for borehole applications |
| EP2495270B1 (en) | 2009-10-30 | 2014-10-01 | Mitsubishi Chemical Corporation | Polyester polyol, polyurethane utilizing the polyester polyol and process for production thereof, and polyurethane molded article |
| JP5269855B2 (ja) * | 2010-10-28 | 2013-08-21 | 株式会社 資生堂 | 化粧料 |
| US20140194589A1 (en) * | 2011-07-08 | 2014-07-10 | Jiangsu Research Institute Of Building Science Co. Ltd | Water-dispersible amphoteric polyurethane, preparation method therefor, and use thereof in reinforcing concrete |
| US20140364552A1 (en) * | 2011-12-09 | 2014-12-11 | Dic Corporation | Aqueous resin composition comprising film-forming aid, and steel sheet surface treatment agent containing the same |
| CN105237721A (zh) * | 2015-09-17 | 2016-01-13 | 合肥思敬齐化工材料有限责任公司 | 一种高附着力水性聚氨酯树脂的制备方法 |
| CN105175671A (zh) * | 2015-09-17 | 2015-12-23 | 合肥思敬齐化工材料有限责任公司 | 一种阴阳离子型聚氨酯树脂及其制备方法 |
| JP2021529235A (ja) * | 2018-06-28 | 2021-10-28 | 日東電工株式会社 | 防汚性ポリマー複合材料 |
| CN115948056B (zh) * | 2022-12-13 | 2024-05-28 | 同济大学 | 端羟基聚丁二烯型聚氨酯改性沥青及其制备方法 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6340726B1 (en) * | 1999-03-03 | 2002-01-22 | Eastman Chemical Company | Silicone polymer diol compositions and condensation polymer/silicone polymer blends |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3509810C1 (de) * | 1985-03-19 | 1986-05-15 | Th. Goldschmidt Ag, 4300 Essen | Verfahren zur Herstellung von Polyurethanformteilen |
| DE69401230T3 (de) | 1993-04-06 | 2006-02-16 | National Starch And Chemical Investment Holding Corp., Wilmington | Verwendung von Polyurethanen, die funktionelle Carboxylatogruppe enthalt, zur Haarfestigung |
| JP3673880B2 (ja) * | 1996-05-29 | 2005-07-20 | 大日本インキ化学工業株式会社 | 水性樹脂水分散体及びその製造方法 |
| JP2950778B2 (ja) * | 1996-07-30 | 1999-09-20 | 日本エヌエスシー株式会社 | 両性ポリウレタン樹脂水分散体の製造方法 |
| JP3972409B2 (ja) * | 1997-05-22 | 2007-09-05 | チッソ株式会社 | コーティング樹脂組成物、及びその硬化方法 |
| JP4165669B2 (ja) | 1998-02-09 | 2008-10-15 | 日本エヌエスシー株式会社 | 化粧品用樹脂組成物およびその製法 |
| DE19821731A1 (de) * | 1998-05-14 | 1999-11-18 | Basf Ag | Kosmetisches Mittel |
| JP4165675B2 (ja) * | 1998-12-22 | 2008-10-15 | 日本エヌエスシー株式会社 | 化粧品用樹脂組成物およびその製法、それを用いた化粧品 |
| JP4165676B2 (ja) * | 1998-12-22 | 2008-10-15 | 日本エヌエスシー株式会社 | 化粧品用樹脂組成物およびその製法、それを用いた化粧品 |
| JP4199353B2 (ja) * | 1998-12-24 | 2008-12-17 | シンジーテック株式会社 | 基材上に多孔質被覆層を形成するための方法 |
| JP2000198920A (ja) * | 1999-01-06 | 2000-07-18 | Nippon Nsc Ltd | 水に分散が容易な新規なポリイソシアネ―ト組成物 |
| FR2793409B1 (fr) * | 1999-05-11 | 2004-03-19 | Oreal | Composition cosmetique comprenant une dispersion aqueuse de polymere filmogene et d'organopolysiloxane |
| JP4104791B2 (ja) | 1999-08-10 | 2008-06-18 | 日本エヌエスシー株式会社 | 化粧料 |
| MXPA01012886A (es) | 2000-04-13 | 2002-07-31 | Nat Starch Chem Invest | Composicion de resina cosmetica y cosmetico que lo usa. |
| JP2003012440A (ja) * | 2001-06-27 | 2003-01-15 | Shiseido Co Ltd | 化粧料 |
-
2001
- 2001-06-27 JP JP2001194685A patent/JP4688351B2/ja not_active Expired - Fee Related
-
2002
- 2002-06-26 MX MXPA02006419A patent/MXPA02006419A/es active IP Right Grant
- 2002-06-26 US US10/183,744 patent/US6646092B2/en not_active Expired - Lifetime
- 2002-06-27 EP EP02014020A patent/EP1275672B1/en not_active Expired - Lifetime
- 2002-06-27 AU AU50677/02A patent/AU783970B2/en not_active Ceased
- 2002-06-27 DE DE60207154T patent/DE60207154T2/de not_active Expired - Lifetime
- 2002-06-27 CN CNB021282358A patent/CN1260263C/zh not_active Expired - Fee Related
- 2002-06-27 BR BR0203347-0A patent/BR0203347A/pt not_active IP Right Cessation
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6340726B1 (en) * | 1999-03-03 | 2002-01-22 | Eastman Chemical Company | Silicone polymer diol compositions and condensation polymer/silicone polymer blends |
Also Published As
| Publication number | Publication date |
|---|---|
| AU5067702A (en) | 2003-01-02 |
| DE60207154D1 (de) | 2005-12-15 |
| JP2003012760A (ja) | 2003-01-15 |
| MXPA02006419A (es) | 2004-08-12 |
| EP1275672B1 (en) | 2005-11-09 |
| US6646092B2 (en) | 2003-11-11 |
| EP1275672A1 (en) | 2003-01-15 |
| BR0203347A (pt) | 2003-05-27 |
| CN1260263C (zh) | 2006-06-21 |
| DE60207154T2 (de) | 2006-08-10 |
| JP4688351B2 (ja) | 2011-05-25 |
| US20030088041A1 (en) | 2003-05-08 |
| CN1406996A (zh) | 2003-04-02 |
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