JP5189363B2 - チオール−ｎｃｏの硬化に基づいたコーティング組成物 - Google Patents
チオール−ｎｃｏの硬化に基づいたコーティング組成物 Download PDFInfo
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- JP5189363B2 JP5189363B2 JP2007531756A JP2007531756A JP5189363B2 JP 5189363 B2 JP5189363 B2 JP 5189363B2 JP 2007531756 A JP2007531756 A JP 2007531756A JP 2007531756 A JP2007531756 A JP 2007531756A JP 5189363 B2 JP5189363 B2 JP 5189363B2
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- coating composition
- acid
- weight
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- oxazolidine
- Prior art date
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- 239000008199 coating composition Substances 0.000 title claims abstract description 41
- 239000005056 polyisocyanate Substances 0.000 claims abstract description 25
- 229920001228 polyisocyanate Polymers 0.000 claims abstract description 25
- 239000003054 catalyst Substances 0.000 claims abstract description 20
- WYNCHZVNFNFDNH-UHFFFAOYSA-N Oxazolidine Chemical compound C1COCN1 WYNCHZVNFNFDNH-UHFFFAOYSA-N 0.000 claims abstract description 18
- 229920006295 polythiol Polymers 0.000 claims abstract description 13
- 239000000463 material Substances 0.000 claims abstract description 12
- 150000004658 ketimines Chemical class 0.000 claims abstract description 4
- 150000004705 aldimines Chemical class 0.000 claims abstract description 3
- 150000002081 enamines Chemical class 0.000 claims abstract description 3
- 238000000576 coating method Methods 0.000 claims description 9
- 238000004132 cross linking Methods 0.000 claims description 6
- 239000012948 isocyanate Substances 0.000 claims description 6
- 239000011248 coating agent Substances 0.000 claims description 5
- 150000007522 mineralic acids Chemical class 0.000 claims description 2
- 125000000160 oxazolidinyl group Chemical group 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
- 239000000203 mixture Substances 0.000 abstract description 24
- 239000000306 component Substances 0.000 description 57
- 150000001875 compounds Chemical class 0.000 description 19
- -1 oxazolidine Chemical class 0.000 description 13
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- 239000005058 Isophorone diisocyanate Substances 0.000 description 3
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- VFHVQBAGLAREND-UHFFFAOYSA-N diphenylphosphoryl-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C)=C1C(=O)P(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 VFHVQBAGLAREND-UHFFFAOYSA-N 0.000 description 3
- 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
- 150000002763 monocarboxylic acids Chemical class 0.000 description 3
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- VUIMBZIZZFSQEE-UHFFFAOYSA-N 1-(1h-indol-3-yl)ethanone Chemical compound C1=CC=C2C(C(=O)C)=CNC2=C1 VUIMBZIZZFSQEE-UHFFFAOYSA-N 0.000 description 2
- XHLHPRDBBAGVEG-UHFFFAOYSA-N 1-tetralone Chemical compound C1=CC=C2C(=O)CCCC2=C1 XHLHPRDBBAGVEG-UHFFFAOYSA-N 0.000 description 2
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 2
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- IMQFZQVZKBIPCQ-UHFFFAOYSA-N 2,2-bis(3-sulfanylpropanoyloxymethyl)butyl 3-sulfanylpropanoate Chemical compound SCCC(=O)OCC(CC)(COC(=O)CCS)COC(=O)CCS IMQFZQVZKBIPCQ-UHFFFAOYSA-N 0.000 description 2
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- 125000005907 alkyl ester group Chemical group 0.000 description 2
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- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
- 150000004795 grignard reagents Chemical class 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- AVIYEYCFMVPYST-UHFFFAOYSA-N hexane-1,3-diol Chemical compound CCCC(O)CCO AVIYEYCFMVPYST-UHFFFAOYSA-N 0.000 description 1
- 238000007757 hot melt coating Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- GJRQTCIYDGXPES-UHFFFAOYSA-N iso-butyl acetate Natural products CC(C)COC(C)=O GJRQTCIYDGXPES-UHFFFAOYSA-N 0.000 description 1
- FGKJLKRYENPLQH-UHFFFAOYSA-M isocaproate Chemical compound CC(C)CCC([O-])=O FGKJLKRYENPLQH-UHFFFAOYSA-M 0.000 description 1
- OQAGVSWESNCJJT-UHFFFAOYSA-N isovaleric acid methyl ester Natural products COC(=O)CC(C)C OQAGVSWESNCJJT-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- VYKXQOYUCMREIS-UHFFFAOYSA-N methylhexahydrophthalic anhydride Chemical compound C1CCCC2C(=O)OC(=O)C21C VYKXQOYUCMREIS-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000013008 moisture curing Methods 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- 150000002791 naphthoquinones Chemical class 0.000 description 1
- HYIMSNHJOBLJNT-UHFFFAOYSA-N nifedipine Chemical compound COC(=O)C1=C(C)NC(C)=C(C(=O)OC)C1C1=CC=CC=C1[N+]([O-])=O HYIMSNHJOBLJNT-UHFFFAOYSA-N 0.000 description 1
- 229960001597 nifedipine Drugs 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 238000007344 nucleophilic reaction Methods 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- FZUGPQWGEGAKET-UHFFFAOYSA-N parbenate Chemical compound CCOC(=O)C1=CC=C(N(C)C)C=C1 FZUGPQWGEGAKET-UHFFFAOYSA-N 0.000 description 1
- 125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
- 150000003003 phosphines Chemical class 0.000 description 1
- 239000003504 photosensitizing agent Substances 0.000 description 1
- IUGYQRQAERSCNH-UHFFFAOYSA-N pivalic acid Chemical compound CC(C)(C)C(O)=O IUGYQRQAERSCNH-UHFFFAOYSA-N 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- WFNXKTMOMOEGSE-UHFFFAOYSA-N propane 2-sulfanylpropanoic acid Chemical compound SC(C(=O)O)C.SC(C(=O)O)C.SC(C(=O)O)C.CCC WFNXKTMOMOEGSE-UHFFFAOYSA-N 0.000 description 1
- LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000007348 radical reaction Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000007665 sagging Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- HYHCSLBZRBJJCH-UHFFFAOYSA-M sodium hydrosulfide Chemical compound [Na+].[SH-] HYHCSLBZRBJJCH-UHFFFAOYSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- UFDHBDMSHIXOKF-UHFFFAOYSA-N tetrahydrophthalic acid Natural products OC(=O)C1=C(C(O)=O)CCCC1 UFDHBDMSHIXOKF-UHFFFAOYSA-N 0.000 description 1
- 239000005028 tinplate Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 description 1
- SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- COIOYMYWGDAQPM-UHFFFAOYSA-N tris(2-methylphenyl)phosphane Chemical compound CC1=CC=CC=C1P(C=1C(=CC=CC=1)C)C1=CC=CC=C1C COIOYMYWGDAQPM-UHFFFAOYSA-N 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- XKGLSKVNOSHTAD-UHFFFAOYSA-N valerophenone Chemical compound CCCCC(=O)C1=CC=CC=C1 XKGLSKVNOSHTAD-UHFFFAOYSA-N 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 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
- C08G18/08—Processes
- C08G18/16—Catalysts
- C08G18/18—Catalysts containing secondary or tertiary amines or salts thereof
- C08G18/20—Heterocyclic amines; Salts thereof
- C08G18/2009—Heterocyclic amines; Salts thereof containing one heterocyclic ring
-
- 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
- C08G18/30—Low-molecular-weight compounds
- C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
-
- 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
- C08G18/30—Low-molecular-weight compounds
- C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
- C08G18/3855—Low-molecular-weight compounds having heteroatoms other than oxygen having sulfur
- C08G18/3876—Low-molecular-weight compounds having heteroatoms other than oxygen having sulfur containing mercapto groups
-
- 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
- C08G18/48—Polyethers
- C08G18/50—Polyethers having heteroatoms other than oxygen
-
- 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)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Paints Or Removers (AREA)
- Polyurethanes Or Polyureas (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP04077582 | 2004-09-17 | ||
| EP04077582.7 | 2004-09-17 | ||
| PCT/EP2005/054628 WO2006030029A1 (en) | 2004-09-17 | 2005-09-16 | Coating composition based on thiol-nco curing |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2008513560A JP2008513560A (ja) | 2008-05-01 |
| JP2008513560A5 JP2008513560A5 (enExample) | 2008-10-02 |
| JP5189363B2 true JP5189363B2 (ja) | 2013-04-24 |
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Family Applications (1)
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|---|---|---|---|
| JP2007531756A Expired - Fee Related JP5189363B2 (ja) | 2004-09-17 | 2005-09-16 | チオール−ｎｃｏの硬化に基づいたコーティング組成物 |
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| EP (1) | EP1789464B1 (enExample) |
| JP (1) | JP5189363B2 (enExample) |
| KR (1) | KR101167892B1 (enExample) |
| CN (1) | CN101044179B (enExample) |
| AT (1) | ATE413421T1 (enExample) |
| AU (1) | AU2005284095B2 (enExample) |
| BR (1) | BRPI0515462A (enExample) |
| CA (1) | CA2580334C (enExample) |
| DE (1) | DE602005010881D1 (enExample) |
| DK (1) | DK1789464T3 (enExample) |
| EA (1) | EA012572B1 (enExample) |
| ES (1) | ES2314717T3 (enExample) |
| IL (1) | IL181979A (enExample) |
| MA (1) | MA28881B1 (enExample) |
| MX (1) | MX2007003197A (enExample) |
| NO (1) | NO20071615L (enExample) |
| NZ (1) | NZ553842A (enExample) |
| PL (1) | PL1789464T3 (enExample) |
| PT (1) | PT1789464E (enExample) |
| UA (1) | UA87704C2 (enExample) |
| WO (1) | WO2006030029A1 (enExample) |
| ZA (1) | ZA200703101B (enExample) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
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| WO2007137608A1 (en) * | 2006-05-31 | 2007-12-06 | Pirelli Tyre S.P.A. | Tire having a coated surface |
| CN101522745B (zh) * | 2006-09-29 | 2013-06-19 | 西巴控股有限公司 | 以封闭异氰酸酯为基础的体系的光潜碱 |
| CA2669578C (en) * | 2006-11-20 | 2015-01-13 | Akzo Nobel Coatings International B.V. | Coating composition |
| BRPI0719116A2 (pt) * | 2006-11-20 | 2013-12-10 | Akzo Nobel Coatings Int Bv | Composição de revestimento |
| US8318830B2 (en) * | 2007-10-17 | 2012-11-27 | Basf Se | Photolatent catalysts based on organometallic compounds |
| US8440736B2 (en) * | 2008-04-07 | 2013-05-14 | University Of Southern Mississippi | Photocuable thiol-ene low gas permeability membranes |
| DE102008026341A1 (de) | 2008-05-07 | 2009-11-12 | Bayer Materialscience Ag | Katalysatoren zur Synthese von Polyurethanen |
| DK2194081T3 (da) * | 2008-12-02 | 2011-12-19 | Sika Technology Ag | Polyurethansammensætning, som indeholder hydroxyaldimin |
| EP2457937A1 (en) | 2010-11-25 | 2012-05-30 | Sika Technology AG | Curing on demand polyurethane composition suitable for the preparation of coatings or floorings |
| DE102012205951B4 (de) * | 2012-04-12 | 2016-09-01 | Chemetall Gmbh | Dichtmassen-System, ungehärtete Grundmasse und Mischung, Härter, Verfahren zum Beschichten eines Substrates und Verwendung eines Dichtmassen-Systems |
| WO2014068998A1 (ja) * | 2012-11-05 | 2014-05-08 | 株式会社ブリヂストン | ゴム積層体及びタイヤ |
| CA2894802C (en) * | 2012-12-11 | 2020-12-22 | Akzo Nobel Coatings International B.V. | Thiol-functional compound |
| WO2014111292A1 (en) | 2013-01-18 | 2014-07-24 | Basf Se | Acrylic dispersion-based coating compositions |
| US9518197B2 (en) | 2014-03-07 | 2016-12-13 | Prc-Desoto International, Inc. | Cure-on-demand moisture-curable urethane-containing fuel resistant prepolymers and compositions thereof |
| US9469607B2 (en) * | 2015-03-03 | 2016-10-18 | Chevron Phillips Chemical Company Lp | Polythiols with carbamate groups |
| US9951252B2 (en) | 2015-08-10 | 2018-04-24 | Prc-Desoto International, Inc. | Moisture-curable fuel-resistant sealant systems |
| JP6197020B2 (ja) * | 2015-12-17 | 2017-09-13 | 三井化学株式会社 | 光硬化性樹脂組成物、表示素子シール剤、液晶シール剤及び液晶表示パネルとその製造方法 |
| US10370561B2 (en) | 2016-06-28 | 2019-08-06 | Prc-Desoto International, Inc. | Urethane/urea-containing bis(alkenyl) ethers, prepolymers prepared using urethane/urea-containing bis(alkenyl) ethers, and uses thereof |
| WO2019105947A1 (en) | 2017-12-01 | 2019-06-06 | Sika Technology Ag | Polyaspartics with long pot life and fast curing |
| CN108892763B (zh) * | 2018-05-28 | 2019-08-30 | 岭南师范学院 | 一种聚氨酯二元硫醇预聚物、光敏树脂组合物及其制备方法和应用 |
| US11098222B2 (en) | 2018-07-03 | 2021-08-24 | Prc-Desoto International, Inc. | Sprayable polythioether coatings and sealants |
| CN109705297B (zh) * | 2018-12-05 | 2021-04-20 | 万华化学集团股份有限公司 | 一种温湿响应快发泡型聚氨酯填充泡沫组合物及制备方法和用途 |
| CN112521573B (zh) * | 2020-11-25 | 2021-07-30 | 山东益丰生化环保股份有限公司 | 一种改性聚硫醇及应用该改性聚硫醇的金属防腐uv涂料 |
| JPWO2024190538A1 (enExample) * | 2023-03-15 | 2024-09-19 | ||
| WO2025131912A1 (en) | 2023-12-22 | 2025-06-26 | Essilor International | Latent borate-ammonium or iminium salts as photo-activatable catalysts for polythiourethane based substrates |
Family Cites Families (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1311211A (en) * | 1919-07-29 | Don carlos brownell | ||
| AT298324B (de) | 1969-04-09 | 1972-05-10 | Minnesota Mining & Mfg | Verfahren zum Abdichten von Betonoberflächen |
| US3789045A (en) * | 1972-11-13 | 1974-01-29 | Gen Mills Chem Inc | Reaction of polyisocyanates with compounds containing blocked amine groups in the presence of acids or metal salts of acids |
| NL7711121A (nl) * | 1977-10-11 | 1979-04-17 | Akzo Nv | Uv-hardbare bekledingscompositie. |
| JPS585370A (ja) * | 1981-07-01 | 1983-01-12 | Takeda Chem Ind Ltd | ポリウレタン塗料・接着剤用組成物 |
| IE56220B1 (en) * | 1984-12-21 | 1991-05-22 | Loctite Ireland Ltd | Conformal coating systems |
| GB9006557D0 (en) | 1990-03-23 | 1990-05-23 | Ici Plc | Polymers |
| US5126421A (en) | 1990-04-27 | 1992-06-30 | 501 Tremco Ltd. | Curing system for isocyanate prepolymers |
| DE4017941A1 (de) * | 1990-06-05 | 1991-12-12 | Univ Schiller Jena | Haertbare zusammensetzung |
| CA2074688A1 (en) | 1991-08-08 | 1993-02-09 | Matthew T. Scholz | Catalysts and casting article, method, and composition |
| US5214086A (en) * | 1991-09-04 | 1993-05-25 | Basf Corporation | Coating compositions which may be ambient cured |
| SE9200564L (sv) | 1992-02-26 | 1993-03-15 | Perstorp Ab | Dendritisk makromolekyl av polyestertyp, foerfarande foer framstaellning daerav samt anvaendning daerav |
| FI955613A7 (fi) | 1993-05-26 | 1995-12-19 | Akzo Nobel Nv | Päällystekoostumus, joka sisältää emäksistä katalyyttiä, josta voidaan poistaa suojaus UV-valolla |
| US5466769A (en) * | 1993-10-26 | 1995-11-14 | Angus Chemical Company | Reactive diluent aldimine oxazolidines |
| DE69531847T2 (de) * | 1994-06-06 | 2004-08-05 | Basf Corp. | Aldimin und Isocyanat enthaltende Beschichtungszusammensetzungen sowie Verfahren zu deren Herstellung |
| MY132867A (en) | 1995-11-24 | 2007-10-31 | Ciba Specialty Chemicals Holding Inc | Acid-stable borates for photopolymerization |
| AU713498B2 (en) | 1996-02-22 | 1999-12-02 | Ciba Specialty Chemicals Holding Inc. | Anionic photocatalyst |
| US6545117B1 (en) * | 1997-08-07 | 2003-04-08 | Akzo Noble N.V. | Sprayable coating compositions comprising an oxazolidine functional compound, an isocyanate functional compound, and a compound selected from a mercapto and a sulfonic acid functional compound |
| WO2000064959A1 (en) | 1999-04-26 | 2000-11-02 | Akzo Nobel N.V. | Composition comprising mercapto-functional compounds |
| KR20020081408A (ko) * | 2000-03-13 | 2002-10-26 | 아크조 노벨 엔.브이. | 이소시아네이트-관능기 화합물, 이소시아네이트-반응성화합물 및 공촉매를 포함하는 조성물 |
| AU6032501A (en) * | 2000-05-26 | 2001-12-11 | Akzo Nobel Nv | Photoactivatable coating composition |
| KR20050055705A (ko) * | 2002-08-13 | 2005-06-13 | 아크조노벨코팅스인터내셔널비.브이. | 티올-관능성 화합물을 포함하는 다층 코팅 시스템 |
-
2005
- 2005-09-16 MX MX2007003197A patent/MX2007003197A/es active IP Right Grant
- 2005-09-16 UA UAA200704229A patent/UA87704C2/uk unknown
- 2005-09-16 KR KR1020077008305A patent/KR101167892B1/ko not_active Expired - Fee Related
- 2005-09-16 NZ NZ553842A patent/NZ553842A/en not_active IP Right Cessation
- 2005-09-16 CN CN2005800355120A patent/CN101044179B/zh not_active Expired - Fee Related
- 2005-09-16 DK DK05794612T patent/DK1789464T3/da active
- 2005-09-16 JP JP2007531756A patent/JP5189363B2/ja not_active Expired - Fee Related
- 2005-09-16 AU AU2005284095A patent/AU2005284095B2/en not_active Ceased
- 2005-09-16 EA EA200700657A patent/EA012572B1/ru not_active IP Right Cessation
- 2005-09-16 PL PL05794612T patent/PL1789464T3/pl unknown
- 2005-09-16 DE DE602005010881T patent/DE602005010881D1/de not_active Expired - Lifetime
- 2005-09-16 BR BRPI0515462-6A patent/BRPI0515462A/pt not_active IP Right Cessation
- 2005-09-16 AT AT05794612T patent/ATE413421T1/de active
- 2005-09-16 PT PT05794612T patent/PT1789464E/pt unknown
- 2005-09-16 WO PCT/EP2005/054628 patent/WO2006030029A1/en not_active Ceased
- 2005-09-16 ES ES05794612T patent/ES2314717T3/es not_active Expired - Lifetime
- 2005-09-16 US US11/663,372 patent/US7709555B2/en not_active Expired - Fee Related
- 2005-09-16 CA CA2580334A patent/CA2580334C/en not_active Expired - Fee Related
- 2005-09-16 EP EP05794612A patent/EP1789464B1/en not_active Expired - Lifetime
-
2007
- 2007-03-15 IL IL181979A patent/IL181979A/en not_active IP Right Cessation
- 2007-03-27 NO NO20071615A patent/NO20071615L/no not_active Application Discontinuation
- 2007-03-29 MA MA29786A patent/MA28881B1/fr unknown
- 2007-04-16 ZA ZA200703101A patent/ZA200703101B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CN101044179A (zh) | 2007-09-26 |
| UA87704C2 (uk) | 2009-08-10 |
| EA012572B1 (ru) | 2009-10-30 |
| WO2006030029A1 (en) | 2006-03-23 |
| DE602005010881D1 (de) | 2008-12-18 |
| MX2007003197A (es) | 2007-05-24 |
| AU2005284095B2 (en) | 2011-04-07 |
| KR20070058606A (ko) | 2007-06-08 |
| JP2008513560A (ja) | 2008-05-01 |
| MA28881B1 (fr) | 2007-09-03 |
| PT1789464E (pt) | 2009-01-23 |
| CA2580334C (en) | 2013-07-02 |
| EP1789464B1 (en) | 2008-11-05 |
| BRPI0515462A (pt) | 2008-07-22 |
| PL1789464T3 (pl) | 2009-04-30 |
| EP1789464A1 (en) | 2007-05-30 |
| NZ553842A (en) | 2009-09-25 |
| ES2314717T3 (es) | 2009-03-16 |
| ATE413421T1 (de) | 2008-11-15 |
| AU2005284095A1 (en) | 2006-03-23 |
| IL181979A0 (en) | 2007-07-04 |
| NO20071615L (no) | 2007-04-16 |
| DK1789464T3 (da) | 2009-03-09 |
| ZA200703101B (en) | 2008-08-27 |
| US7709555B2 (en) | 2010-05-04 |
| EA200700657A1 (ru) | 2007-08-31 |
| CN101044179B (zh) | 2011-07-06 |
| US20080194720A1 (en) | 2008-08-14 |
| IL181979A (en) | 2013-01-31 |
| KR101167892B1 (ko) | 2012-07-30 |
| CA2580334A1 (en) | 2006-03-23 |
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