CN102030883A - 包含脲基甲酸酯和硅烷基团的高官能度多异氰酸酯 - Google Patents
包含脲基甲酸酯和硅烷基团的高官能度多异氰酸酯 Download PDFInfo
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- CN102030883A CN102030883A CN2010105406460A CN201010540646A CN102030883A CN 102030883 A CN102030883 A CN 102030883A CN 2010105406460 A CN2010105406460 A CN 2010105406460A CN 201010540646 A CN201010540646 A CN 201010540646A CN 102030883 A CN102030883 A CN 102030883A
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- polyisocyanates
- carbon atoms
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- 239000005056 polyisocyanate Substances 0.000 title claims abstract description 72
- 229920001228 polyisocyanate Polymers 0.000 title claims abstract description 72
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical group [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 title claims abstract description 45
- 238000000034 method Methods 0.000 claims abstract description 72
- 238000002360 preparation method Methods 0.000 claims abstract description 18
- 229920003023 plastic Polymers 0.000 claims abstract description 6
- 239000004033 plastic Substances 0.000 claims abstract description 6
- 238000006243 chemical reaction Methods 0.000 claims description 49
- -1 4Be hydrogen Chemical class 0.000 claims description 44
- 125000004432 carbon atom Chemical group C* 0.000 claims description 42
- VSKFADHADUWCCL-UHFFFAOYSA-N carbamoperoxoic acid Chemical compound NC(=O)OO VSKFADHADUWCCL-UHFFFAOYSA-N 0.000 claims description 30
- 125000001931 aliphatic group Chemical group 0.000 claims description 26
- 150000002596 lactones Chemical class 0.000 claims description 26
- 239000000203 mixture Substances 0.000 claims description 25
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 claims description 22
- 150000005676 cyclic carbonates Chemical class 0.000 claims description 21
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 20
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 19
- 125000002723 alicyclic group Chemical group 0.000 claims description 16
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 15
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- 125000003118 aryl group Chemical group 0.000 claims description 13
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 12
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- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 10
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- 229910052757 nitrogen Inorganic materials 0.000 claims description 10
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 9
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 claims description 6
- 125000003545 alkoxy group Chemical group 0.000 claims description 6
- 125000001118 alkylidene group Chemical group 0.000 claims description 6
- 239000003153 chemical reaction reagent Substances 0.000 claims description 6
- 125000005442 diisocyanate group Chemical group 0.000 claims description 6
- JBFHTYHTHYHCDJ-UHFFFAOYSA-N gamma-caprolactone Chemical compound CCC1CCC(=O)O1 JBFHTYHTHYHCDJ-UHFFFAOYSA-N 0.000 claims description 6
- 239000001301 oxygen Substances 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- VEZXCJBBBCKRPI-UHFFFAOYSA-N beta-propiolactone Chemical compound O=C1CCO1 VEZXCJBBBCKRPI-UHFFFAOYSA-N 0.000 claims description 5
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- 239000000865 liniment Substances 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
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- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 claims description 5
- ZWVMLYRJXORSEP-LURJTMIESA-N (2s)-hexane-1,2,6-triol Chemical compound OCCCC[C@H](O)CO ZWVMLYRJXORSEP-LURJTMIESA-N 0.000 claims description 4
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- 230000015572 biosynthetic process Effects 0.000 claims description 4
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- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
- 239000005864 Sulphur Substances 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 125000005842 heteroatom Chemical group 0.000 claims description 3
- XXKOQQBKBHUATC-UHFFFAOYSA-N cyclohexylmethylcyclohexane Chemical compound C1CCCCC1CC1CCCCC1 XXKOQQBKBHUATC-UHFFFAOYSA-N 0.000 claims description 2
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- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 22
- 239000011248 coating agent Substances 0.000 description 22
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 22
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- 229910000077 silane Inorganic materials 0.000 description 21
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- 229910021529 ammonia Inorganic materials 0.000 description 10
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- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 9
- 241001550224 Apha Species 0.000 description 9
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
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- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 9
- 239000002585 base Substances 0.000 description 8
- 239000003054 catalyst Substances 0.000 description 8
- 238000001035 drying Methods 0.000 description 8
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical group NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 7
- 150000001412 amines Chemical class 0.000 description 7
- 229920005862 polyol Polymers 0.000 description 7
- 150000003077 polyols Chemical class 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- 239000012948 isocyanate Substances 0.000 description 6
- 150000002513 isocyanates Chemical class 0.000 description 6
- 229920005906 polyester polyol Polymers 0.000 description 6
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 108010064470 polyaspartate Proteins 0.000 description 5
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- 238000004448 titration Methods 0.000 description 5
- 229940058015 1,3-butylene glycol Drugs 0.000 description 4
- UXFQFBNBSPQBJW-UHFFFAOYSA-N 2-amino-2-methylpropane-1,3-diol Chemical compound OCC(N)(C)CO UXFQFBNBSPQBJW-UHFFFAOYSA-N 0.000 description 4
- SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical group CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 239000004721 Polyphenylene oxide Substances 0.000 description 4
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- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 4
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 4
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- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 235000019437 butane-1,3-diol Nutrition 0.000 description 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 4
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- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 3
- OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical compound CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 description 3
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
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- 239000004411 aluminium Substances 0.000 description 3
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- 125000004103 aminoalkyl group Chemical group 0.000 description 3
- 229940009098 aspartate Drugs 0.000 description 3
- DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical compound CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 3
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- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
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Classifications
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- C08G18/8009—Masked polyisocyanates masked with compounds having at least two groups containing active hydrogen with compounds of C08G18/32 with compounds of C08G18/3203
- C08G18/8012—Masked polyisocyanates masked with compounds having at least two groups containing active hydrogen with compounds of C08G18/32 with compounds of C08G18/3203 with diols
- C08G18/8016—Masked aliphatic or cycloaliphatic polyisocyanates
-
- 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
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/80—Masked polyisocyanates
- C08G18/8061—Masked polyisocyanates masked with compounds having only one group containing active hydrogen
- C08G18/8083—Masked polyisocyanates masked with compounds having only one group containing active hydrogen with compounds containing at least one heteroatom other than oxygen or nitrogen
- C08G18/809—Masked polyisocyanates masked with compounds having only one group containing active hydrogen with compounds containing at least one heteroatom other than oxygen or nitrogen containing silicon
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/02—Polyureas
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Polyurethanes Or Polyureas (AREA)
- Paints Or Removers (AREA)
Abstract
Description
Claims (17)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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DE102009047964.3 | 2009-10-01 | ||
DE102009047964A DE102009047964A1 (de) | 2009-10-01 | 2009-10-01 | Hochfunktionelle Allophanat- und Silangruppen enthaltende Polyisocyanate |
Publications (2)
Publication Number | Publication Date |
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CN102030883A true CN102030883A (zh) | 2011-04-27 |
CN102030883B CN102030883B (zh) | 2015-02-11 |
Family
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US (1) | US20110082273A1 (zh) |
EP (1) | EP2305691B1 (zh) |
JP (1) | JP5751789B2 (zh) |
KR (1) | KR20110036511A (zh) |
CN (1) | CN102030883B (zh) |
CA (1) | CA2716087A1 (zh) |
DE (1) | DE102009047964A1 (zh) |
ES (1) | ES2386528T3 (zh) |
PL (1) | PL2305691T3 (zh) |
PT (1) | PT2305691E (zh) |
RU (1) | RU2539985C2 (zh) |
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Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4160080A (en) * | 1977-07-02 | 1979-07-03 | Bayer Aktiengesellschaft | Process for the preparation of allophanates which contain isocyanate groups |
US4810820A (en) * | 1987-08-12 | 1989-03-07 | Mobay Corporation | Process for the production of polyisocyanates containing allophanate groups |
CN101381443A (zh) * | 2007-07-13 | 2009-03-11 | 拜尔材料科学股份公司 | 包含脲基甲酸酯和硅烷基团的多异氰酸酯 |
Family Cites Families (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SU29574A1 (ru) | 1932-05-10 | 1933-03-31 | А.М. Кульбицкий | Устройство дл хранени одежды в общественных местах |
GB994890A (en) | 1961-12-18 | 1965-06-10 | Ici Ltd | New organic polyisocyanates and their manufacture |
DE1770245C3 (de) | 1968-04-23 | 1979-11-15 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von gegebenenfalls vernetzten Polyurethanen |
DE2009179C3 (de) | 1970-02-27 | 1974-07-11 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von Allophanatpoly isocy anaten |
US4104296A (en) | 1970-09-28 | 1978-08-01 | Union Carbide Corporation | Organofunctional silicon compounds |
ES2062188T3 (es) | 1989-06-23 | 1994-12-16 | Bayer Ag | Procedimiento para la elaboracion de revestimientos. |
DE4136618A1 (de) | 1991-11-07 | 1993-05-13 | Bayer Ag | Wasserdispergierbare polyisocyanatgemische |
DE4237468A1 (de) | 1992-11-06 | 1994-05-11 | Bayer Ag | Alkoxysilan- und Aminogruppen aufweisende Verbindungen |
DE4335796A1 (de) | 1993-10-20 | 1995-04-27 | Bayer Ag | Lackpolyisocyanate und ihre Verwendung |
DE4416321A1 (de) * | 1994-05-09 | 1995-11-16 | Bayer Ag | Verfahren zur Herstellung von Allophanatgruppen aufweisenden lichtechten Polyisocyanaten |
US5587502A (en) | 1995-06-02 | 1996-12-24 | Minnesota Mining & Manufacturing Company | Hydroxy functional alkoxysilane and alkoxysilane functional polyurethane made therefrom |
US5866651A (en) | 1996-10-31 | 1999-02-02 | Minnesota Mining And Manufacturing Company | Hydroxycarbamoylalkoxysilane-based poly(ether-urethane) sealants having improved paint adhesion and laminates prepared therefrom |
DE19715427A1 (de) | 1997-04-14 | 1998-10-15 | Bayer Ag | Wäßrige 2-Komponenten Bindemittel und deren Verwendung |
US6057415A (en) | 1998-04-09 | 2000-05-02 | Bayer Corporation | Water dispersible polyisocyanates containing alkoxysilane groups |
ES2209274T3 (es) | 1998-05-22 | 2004-06-16 | Bayer Aktiengesellschaft | Mezclas de poliisocianatos modificadas mediante polieteres dispersables. |
US6005047A (en) | 1998-10-14 | 1999-12-21 | Bayer Corporation | Moisture-curable compounds containing isocyanate and alkoxysilane groups |
CZ20012081A3 (cs) * | 1998-12-11 | 2001-09-12 | Henkel Kommanditgesellschaft Auf Aktien | Disperze polymerů s koncovými silylovými skupinami |
DE10024624A1 (de) | 2000-05-18 | 2001-11-22 | Bayer Ag | Modifizierte Polyisocyanate |
DE10103026A1 (de) | 2001-01-24 | 2002-07-25 | Bayer Ag | Schutzüberzug mit zweischichtigem Beschichtungsaufbau |
DE10130882A1 (de) | 2001-06-27 | 2003-01-16 | Bayer Ag | Verfahren zur Herstellung von aliphatischen Oligocarbonatdiolen |
DE10132938A1 (de) | 2001-07-06 | 2003-01-16 | Degussa | Nichtwässriges, wärmehärtendes Zweikomponenten-Beschichtungsmittel |
DE10162642A1 (de) | 2001-12-20 | 2003-07-10 | Henkel Kgaa | Haftvermittler für reaktive Polyurethane |
JP2005015644A (ja) | 2003-06-26 | 2005-01-20 | Yokohama Rubber Co Ltd:The | 新規化合物およびそれを含有する硬化性樹脂組成物 |
DE10353663A1 (de) * | 2003-11-17 | 2005-06-16 | Henkel Kgaa | Polyurethanzusammensetzungen mit NCO- und Silylreaktivität |
US20050208312A1 (en) * | 2004-03-17 | 2005-09-22 | Isidor Hazan | One-pack primer surfacer composition for SMC automotive body panels |
US7435787B2 (en) * | 2005-09-14 | 2008-10-14 | Momentive Performance Materials Inc. | Process for the continuous production of silylated resin |
JP4886429B2 (ja) * | 2006-08-30 | 2012-02-29 | 関西ペイント株式会社 | 水性樹脂組成物及びこれを含む水性塗料組成物 |
DE102009016173A1 (de) | 2009-04-03 | 2010-10-14 | Bayer Materialscience Ag | Schutzlack |
-
2009
- 2009-10-01 DE DE102009047964A patent/DE102009047964A1/de not_active Withdrawn
-
2010
- 2010-09-18 EP EP10009877A patent/EP2305691B1/de not_active Not-in-force
- 2010-09-18 ES ES10009877T patent/ES2386528T3/es active Active
- 2010-09-18 PT PT10009877T patent/PT2305691E/pt unknown
- 2010-09-18 PL PL10009877T patent/PL2305691T3/pl unknown
- 2010-09-28 CA CA2716087A patent/CA2716087A1/en not_active Abandoned
- 2010-09-30 CN CN201010540646.0A patent/CN102030883B/zh not_active Expired - Fee Related
- 2010-09-30 RU RU2010140104/04A patent/RU2539985C2/ru not_active IP Right Cessation
- 2010-09-30 US US12/894,348 patent/US20110082273A1/en not_active Abandoned
- 2010-09-30 KR KR1020100095022A patent/KR20110036511A/ko not_active Application Discontinuation
- 2010-10-01 JP JP2010223672A patent/JP5751789B2/ja not_active Expired - Fee Related
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4160080A (en) * | 1977-07-02 | 1979-07-03 | Bayer Aktiengesellschaft | Process for the preparation of allophanates which contain isocyanate groups |
US4810820A (en) * | 1987-08-12 | 1989-03-07 | Mobay Corporation | Process for the production of polyisocyanates containing allophanate groups |
CN101381443A (zh) * | 2007-07-13 | 2009-03-11 | 拜尔材料科学股份公司 | 包含脲基甲酸酯和硅烷基团的多异氰酸酯 |
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CN103917568A (zh) * | 2011-10-27 | 2014-07-09 | 帝斯曼知识产权资产管理有限公司 | 聚合物、组合物及其制备方法 |
US9850260B2 (en) | 2013-07-30 | 2017-12-26 | Sika Technology Ag | Hydroxymethyl-carboxamido-substituted silane and its use for curable, silane-terminated polymers |
CN105408337A (zh) * | 2013-07-30 | 2016-03-16 | Sika技术股份公司 | 用于可固化的硅烷封端的聚合物的羟甲基羧酰氨基取代的硅烷醇 |
CN105408337B (zh) * | 2013-07-30 | 2020-03-24 | Sika技术股份公司 | 用于可固化的硅烷封端的聚合物的羟甲基羧酰氨基取代的硅烷醇 |
CN105705668A (zh) * | 2013-10-01 | 2016-06-22 | 比尔德兰德株式会社 | 金属喷镀方法 |
CN105934437A (zh) * | 2014-01-31 | 2016-09-07 | 科思创德国股份有限公司 | 硅烷改性的甲酰胺 |
CN105934437B (zh) * | 2014-01-31 | 2019-03-01 | 科思创德国股份有限公司 | 硅烷改性的甲酰胺 |
CN104004398A (zh) * | 2014-05-26 | 2014-08-27 | 北京化工大学 | 一种海水淡化工程中聚脲防腐涂料用催化剂 |
CN106414540A (zh) * | 2014-06-13 | 2017-02-15 | 科思创德国股份有限公司 | 含硅烷基团的硫代脲基甲酸酯多异氰酸酯 |
CN106414540B (zh) * | 2014-06-13 | 2020-04-24 | 科思创德国股份有限公司 | 含硅烷基团的硫代脲基甲酸酯多异氰酸酯 |
CN107001556A (zh) * | 2014-11-24 | 2017-08-01 | Sika技术股份公司 | 含有硅烷基团的快速固化组合物 |
CN107001556B (zh) * | 2014-11-24 | 2020-12-22 | Sika技术股份公司 | 含有硅烷基团的快速固化组合物 |
CN107922574A (zh) * | 2015-09-09 | 2018-04-17 | 科思创德国股份有限公司 | 耐划伤水性2k pu涂料 |
CN108350308A (zh) * | 2015-11-03 | 2018-07-31 | 巴斯夫涂料有限公司 | 作为反应性稀释剂的生物基羟基氨基甲酸乙酯 |
CN114044896B (zh) * | 2016-05-13 | 2023-08-08 | 国立科学研究中心 | 均匀序列定义的聚氨酯及其作为分子标记的用途 |
CN114044896A (zh) * | 2016-05-13 | 2022-02-15 | 国立科学研究中心 | 均匀序列定义的聚氨酯及其作为分子标记的用途 |
CN106279241A (zh) * | 2016-07-16 | 2017-01-04 | 北京化工大学 | 一种含硅氧烷结构的单官能度丙烯酸酯单体及其制备方法 |
CN112996797B (zh) * | 2018-11-09 | 2024-07-12 | 博斯蒂克股份公司 | 官能化羟基硅烷,硅烷化聚氨酯和包括其的组合物 |
CN112996797A (zh) * | 2018-11-09 | 2021-06-18 | 博斯蒂克股份公司 | 官能化羟基硅烷,硅烷化聚氨酯和包括其的组合物 |
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ES2386528T3 (es) | 2012-08-22 |
JP5751789B2 (ja) | 2015-07-22 |
KR20110036511A (ko) | 2011-04-07 |
RU2010140104A (ru) | 2012-04-10 |
EP2305691A1 (de) | 2011-04-06 |
JP2011074390A (ja) | 2011-04-14 |
PT2305691E (pt) | 2012-07-24 |
PL2305691T3 (pl) | 2012-10-31 |
CA2716087A1 (en) | 2011-04-01 |
DE102009047964A1 (de) | 2011-04-21 |
CN102030883B (zh) | 2015-02-11 |
EP2305691B1 (de) | 2012-05-30 |
RU2539985C2 (ru) | 2015-01-27 |
US20110082273A1 (en) | 2011-04-07 |
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