JP5496440B2 - 常温硬化型塗料及びそれらが塗布されたゴム製品 - Google Patents
常温硬化型塗料及びそれらが塗布されたゴム製品 Download PDFInfo
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- JP5496440B2 JP5496440B2 JP2005505620A JP2005505620A JP5496440B2 JP 5496440 B2 JP5496440 B2 JP 5496440B2 JP 2005505620 A JP2005505620 A JP 2005505620A JP 2005505620 A JP2005505620 A JP 2005505620A JP 5496440 B2 JP5496440 B2 JP 5496440B2
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- acrylate
- film
- acid
- functional
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- 229920001971 elastomer Polymers 0.000 title claims description 77
- 239000003973 paint Substances 0.000 title claims description 36
- 239000005060 rubber Substances 0.000 title claims description 34
- -1 methylol functional groups Chemical group 0.000 claims description 159
- 229920000642 polymer Polymers 0.000 claims description 138
- 239000000178 monomer Substances 0.000 claims description 88
- 125000000524 functional group Chemical group 0.000 claims description 81
- 229920001577 copolymer Polymers 0.000 claims description 65
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 57
- 239000001257 hydrogen Substances 0.000 claims description 34
- 229910052739 hydrogen Inorganic materials 0.000 claims description 34
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 30
- 150000001993 dienes Chemical class 0.000 claims description 30
- 238000005984 hydrogenation reaction Methods 0.000 claims description 27
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- 239000000203 mixture Substances 0.000 claims description 26
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- 238000000576 coating method Methods 0.000 claims description 21
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 20
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 17
- 239000011248 coating agent Substances 0.000 claims description 17
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- 125000005647 linker group Chemical group 0.000 claims description 10
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- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 3
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- 125000005250 alkyl acrylate group Chemical group 0.000 claims description 3
- 229920003048 styrene butadiene rubber Polymers 0.000 claims description 3
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- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 2
- DOUHZFSGSXMPIE-UHFFFAOYSA-N hydroxidooxidosulfur(.) Chemical compound [O]SO DOUHZFSGSXMPIE-UHFFFAOYSA-N 0.000 claims 2
- 125000003504 2-oxazolinyl group Chemical group O1C(=NCC1)* 0.000 claims 1
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- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 claims 1
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- 229920002587 poly(1,3-butadiene) polymer Polymers 0.000 claims 1
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- 125000004432 carbon atom Chemical group C* 0.000 description 28
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 28
- 229920001973 fluoroelastomer Polymers 0.000 description 26
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- 238000004132 cross linking Methods 0.000 description 24
- 150000002148 esters Chemical class 0.000 description 23
- 239000002253 acid Substances 0.000 description 22
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- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 21
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 21
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- 239000000243 solution Substances 0.000 description 20
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 19
- 239000003054 catalyst Substances 0.000 description 19
- 239000002904 solvent Substances 0.000 description 19
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 18
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 18
- 239000000758 substrate Substances 0.000 description 18
- 238000006116 polymerization reaction Methods 0.000 description 17
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 16
- 239000005977 Ethylene Substances 0.000 description 15
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 15
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
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- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 14
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- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 14
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 14
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 14
- 239000000463 material Substances 0.000 description 14
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 13
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 13
- 238000007306 functionalization reaction Methods 0.000 description 13
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 13
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 12
- 239000003999 initiator Substances 0.000 description 12
- 239000011976 maleic acid Substances 0.000 description 12
- 229920000058 polyacrylate Polymers 0.000 description 12
- 239000000047 product Substances 0.000 description 12
- 229920002554 vinyl polymer Polymers 0.000 description 12
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 11
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 11
- 229920002367 Polyisobutene Polymers 0.000 description 11
- 125000003545 alkoxy group Chemical group 0.000 description 11
- 150000001408 amides Chemical class 0.000 description 11
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- 229910052751 metal Inorganic materials 0.000 description 11
- 239000002184 metal Substances 0.000 description 11
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 11
- 239000002243 precursor Substances 0.000 description 11
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 10
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 description 10
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- 229910052782 aluminium Inorganic materials 0.000 description 9
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 9
- 125000003277 amino group Chemical group 0.000 description 9
- 229910052799 carbon Inorganic materials 0.000 description 9
- 239000000460 chlorine Substances 0.000 description 9
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- 229910052736 halogen Inorganic materials 0.000 description 9
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- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 9
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- 239000004215 Carbon black (E152) Substances 0.000 description 8
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 8
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- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 8
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 8
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- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 8
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- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 6
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- 125000004122 cyclic group Chemical group 0.000 description 4
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- 150000003573 thiols Chemical class 0.000 description 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
- YIYBQIKDCADOSF-ONEGZZNKSA-N trans-pent-2-enoic acid Chemical compound CC\C=C\C(O)=O YIYBQIKDCADOSF-ONEGZZNKSA-N 0.000 description 1
- 238000005891 transamination reaction Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 238000000844 transformation Methods 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- GQIUQDDJKHLHTB-UHFFFAOYSA-N trichloro(ethenyl)silane Chemical compound Cl[Si](Cl)(Cl)C=C GQIUQDDJKHLHTB-UHFFFAOYSA-N 0.000 description 1
- HKFSBKQQYCMCKO-UHFFFAOYSA-N trichloro(prop-2-enyl)silane Chemical compound Cl[Si](Cl)(Cl)CC=C HKFSBKQQYCMCKO-UHFFFAOYSA-N 0.000 description 1
- FAQYAMRNWDIXMY-UHFFFAOYSA-N trichloroborane Chemical compound ClB(Cl)Cl FAQYAMRNWDIXMY-UHFFFAOYSA-N 0.000 description 1
- ZDHXKXAHOVTTAH-UHFFFAOYSA-N trichlorosilane Chemical compound Cl[SiH](Cl)Cl ZDHXKXAHOVTTAH-UHFFFAOYSA-N 0.000 description 1
- 239000005052 trichlorosilane Substances 0.000 description 1
- 229960001124 trientine Drugs 0.000 description 1
- BULZRBYTOVVERT-UHFFFAOYSA-N trihydroxysilylamine Chemical class N[Si](O)(O)O BULZRBYTOVVERT-UHFFFAOYSA-N 0.000 description 1
- YUYCVXFAYWRXLS-UHFFFAOYSA-N trimethoxysilane Chemical compound CO[SiH](OC)OC YUYCVXFAYWRXLS-UHFFFAOYSA-N 0.000 description 1
- UAIFZYSPVVBOPN-UHFFFAOYSA-N trimethyl(prop-1-en-2-yloxy)silane Chemical compound CC(=C)O[Si](C)(C)C UAIFZYSPVVBOPN-UHFFFAOYSA-N 0.000 description 1
- MNMVKGDEKPPREK-UHFFFAOYSA-N trimethyl(prop-2-enoxy)silane Chemical compound C[Si](C)(C)OCC=C MNMVKGDEKPPREK-UHFFFAOYSA-N 0.000 description 1
- UYPYRKYUKCHHIB-UHFFFAOYSA-N trimethylamine N-oxide Chemical compound C[N+](C)(C)[O-] UYPYRKYUKCHHIB-UHFFFAOYSA-N 0.000 description 1
- 229940094989 trimethylsilane Drugs 0.000 description 1
- PGQNYIRJCLTTOJ-UHFFFAOYSA-N trimethylsilyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)O[Si](C)(C)C PGQNYIRJCLTTOJ-UHFFFAOYSA-N 0.000 description 1
- CWMFRHBXRUITQE-UHFFFAOYSA-N trimethylsilylacetylene Chemical group C[Si](C)(C)C#C CWMFRHBXRUITQE-UHFFFAOYSA-N 0.000 description 1
- DSROZUMNVRXZNO-UHFFFAOYSA-K tris[(1-naphthalen-1-yl-3-phenylnaphthalen-2-yl)oxy]alumane Chemical compound C=1C=CC=CC=1C=1C=C2C=CC=CC2=C(C=2C3=CC=CC=C3C=CC=2)C=1O[Al](OC=1C(=C2C=CC=CC2=CC=1C=1C=CC=CC=1)C=1C2=CC=CC=C2C=CC=1)OC(C(=C1C=CC=CC1=C1)C=2C3=CC=CC=C3C=CC=2)=C1C1=CC=CC=C1 DSROZUMNVRXZNO-UHFFFAOYSA-K 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 239000005050 vinyl trichlorosilane Substances 0.000 description 1
- UKRDPEFKFJNXQM-UHFFFAOYSA-N vinylsilane Chemical class [SiH3]C=C UKRDPEFKFJNXQM-UHFFFAOYSA-N 0.000 description 1
- 239000004636 vulcanized rubber Substances 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
- XKMZOFXGLBYJLS-UHFFFAOYSA-L zinc;prop-2-enoate Chemical compound [Zn+2].[O-]C(=O)C=C.[O-]C(=O)C=C XKMZOFXGLBYJLS-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- 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
- C09D115/00—Coating compositions based on rubber derivatives
- C09D115/005—Hydrogenated nitrile rubber
-
- 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
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/0427—Coating with only one layer of a composition containing a polymer binder
-
- 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
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/043—Improving the adhesiveness of the coatings per se, e.g. forming primers
-
- 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
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/046—Forming abrasion-resistant coatings; Forming surface-hardening coatings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/02—Elements
- C08K3/08—Metals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/54—Silicon-containing compounds
- C08K5/544—Silicon-containing compounds containing nitrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L15/00—Compositions of rubber derivatives
- C08L15/005—Hydrogenated nitrile rubber
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L21/00—Compositions of unspecified rubbers
-
- 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
- C08J2321/00—Characterised by the use of unspecified rubbers
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)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/205,178 | 2002-07-25 | ||
| US10/205,178 US6844412B2 (en) | 2002-07-25 | 2002-07-25 | Ambient cured coatings and coated rubber products therefrom |
| US10/265,576 US6777026B2 (en) | 2002-10-07 | 2002-10-07 | Flexible emissive coatings for elastomer substrates |
| US10/265,576 | 2002-10-07 | ||
| PCT/US2003/023360 WO2004011536A1 (en) | 2002-07-25 | 2003-07-24 | Ambient cured coatings and coated rubber products therefrom |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013224965A Division JP2014051672A (ja) | 2002-07-25 | 2013-10-30 | 常温硬化型塗料及びそれらが塗布されたゴム製品 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2005533923A JP2005533923A (ja) | 2005-11-10 |
| JP2005533923A5 JP2005533923A5 (enExample) | 2013-12-19 |
| JP5496440B2 true JP5496440B2 (ja) | 2014-05-21 |
Family
ID=31190679
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2005505620A Expired - Fee Related JP5496440B2 (ja) | 2002-07-25 | 2003-07-24 | 常温硬化型塗料及びそれらが塗布されたゴム製品 |
| JP2013224965A Withdrawn JP2014051672A (ja) | 2002-07-25 | 2013-10-30 | 常温硬化型塗料及びそれらが塗布されたゴム製品 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013224965A Withdrawn JP2014051672A (ja) | 2002-07-25 | 2013-10-30 | 常温硬化型塗料及びそれらが塗布されたゴム製品 |
Country Status (10)
| Country | Link |
|---|---|
| EP (1) | EP1490427B1 (enExample) |
| JP (2) | JP5496440B2 (enExample) |
| KR (1) | KR101021533B1 (enExample) |
| CN (1) | CN100419007C (enExample) |
| BR (1) | BR0311798B1 (enExample) |
| CA (1) | CA2492866A1 (enExample) |
| DE (1) | DE60304208T2 (enExample) |
| ES (1) | ES2256784T3 (enExample) |
| MX (1) | MXPA04011464A (enExample) |
| WO (1) | WO2004011536A1 (enExample) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100335579C (zh) * | 2002-03-08 | 2007-09-05 | 洛德公司 | 用于弹性体基材的柔性涂层和涂覆弹性体模制品的方法 |
| US6777026B2 (en) * | 2002-10-07 | 2004-08-17 | Lord Corporation | Flexible emissive coatings for elastomer substrates |
| US7220487B2 (en) * | 2002-07-25 | 2007-05-22 | Lord Corporation | Ambient cured flexible fluoroelastomer coatings and coated products |
| US20060110559A1 (en) * | 2004-10-05 | 2006-05-25 | Victor Nasreddine | Crosslinking of carboxylated nitrile polymers with organo functional silanes: a curable plasticizer composition |
| DE102005038794A1 (de) * | 2005-08-17 | 2007-02-22 | Degussa Ag | Kautschukmischungen |
| SG157237A1 (en) * | 2008-05-13 | 2009-12-29 | Sumitomo Bakelite Singapore Pte Ltd | A curable composition |
| DE102008002250A1 (de) * | 2008-06-06 | 2009-12-10 | Robert Bosch Gmbh | Beschichtungsmaterial für Elastomermaterialien |
| EP2386600B1 (de) * | 2010-04-15 | 2013-06-19 | LANXESS Deutschland GmbH | Isocyanatgruppen-enthaltende Vernetzer für Nitrilkautschuke |
| CN101942270B (zh) * | 2010-10-21 | 2012-07-04 | 江苏科技大学 | 一种用于led灯的散热涂料 |
| EP2484700B1 (de) * | 2011-02-04 | 2013-10-09 | LANXESS Deutschland GmbH | Funktionalisierte Nitrilkautschuke und ihre Herstellung |
| RU2494130C1 (ru) * | 2012-06-09 | 2013-09-27 | Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Волгоградский государственный технический университет" (ВолгГТУ) | Композиция для покрытий |
| RU2493187C1 (ru) * | 2012-06-09 | 2013-09-20 | Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Волгоградский государственный технический университет" (ВолгГТУ) | Композиция для покрытий |
| RU2503698C1 (ru) * | 2012-06-09 | 2014-01-10 | Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Волгоградский государственный технический университет" (ВолгГТУ) | Композиция для покрытий |
| RU2547019C1 (ru) * | 2014-02-11 | 2015-04-10 | Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Волгоградский государственный технический университет" (ВолгГТУ) | Композиция для покрытий |
| RU2546737C1 (ru) * | 2014-02-11 | 2015-04-10 | Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Волгоградский государственный технический университет" (ВолгГТУ) | Композиция для покрытий |
| DE102014107048B4 (de) * | 2014-05-19 | 2019-07-18 | Ahauser Gummiwalzen Lammers Gmbh & Co. Kg | Verbundwalze mit einem dehäsiven Walzenbezug |
| KR101640897B1 (ko) * | 2015-09-16 | 2016-07-29 | 주식회사 지에이치비 | 주낙통 접합기 및 주낙통 접합방법 |
| EP3592789B1 (en) * | 2017-03-08 | 2023-05-03 | Bridgestone Corporation | Coupled polymer products, methods of making and compositions containing |
| EP3387931B1 (de) * | 2017-04-10 | 2020-07-15 | ARLANXEO Deutschland GmbH | Vulkanisierbare zusammensetzung enthaltend hxnbr-latex und polyfunktionales epoxid |
| CN111866669B (zh) * | 2019-04-24 | 2021-11-16 | 歌尔股份有限公司 | 一种用于微型发声装置的振膜和微型发声装置 |
| US11242430B2 (en) | 2019-10-17 | 2022-02-08 | Ppg Industries Ohio, Inc. | Crosslinking compositions and coatings formed therefrom |
| CN115677965B (zh) * | 2022-09-15 | 2023-07-04 | 南京贝迪新材料科技股份有限公司 | 一种高性能量子点复合物的制备方法 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4670496A (en) * | 1984-06-13 | 1987-06-02 | The Goodyear Tire & Rubber Company | Coating material for use on sulfur vulcanized rubber |
| EP0563835A1 (en) * | 1992-03-30 | 1993-10-06 | JMK International Inc. | Flexible heat-resistant reflective paint, and painted elastomeric components |
| JPH0931396A (ja) * | 1995-07-17 | 1997-02-04 | Japan Synthetic Rubber Co Ltd | コーティング用水分散体 |
| JPH09208890A (ja) * | 1996-02-07 | 1997-08-12 | Toshiba Silicone Co Ltd | ゴム物品 |
| CA2302869A1 (en) * | 1999-03-29 | 2000-09-29 | Kaneka Corporation | One-pack type curable resin composition |
| JP2000313839A (ja) * | 1999-04-28 | 2000-11-14 | Toagosei Co Ltd | フッ素ゴム系塗料用組成物 |
| US6709758B2 (en) * | 2001-11-09 | 2004-03-23 | Lord Corporation | Room temperature curable X-HNBR coating |
| CN100335579C (zh) * | 2002-03-08 | 2007-09-05 | 洛德公司 | 用于弹性体基材的柔性涂层和涂覆弹性体模制品的方法 |
| US6777026B2 (en) * | 2002-10-07 | 2004-08-17 | Lord Corporation | Flexible emissive coatings for elastomer substrates |
| US6844412B2 (en) * | 2002-07-25 | 2005-01-18 | Lord Corporation | Ambient cured coatings and coated rubber products therefrom |
-
2003
- 2003-07-24 KR KR1020047016406A patent/KR101021533B1/ko not_active Expired - Fee Related
- 2003-07-24 WO PCT/US2003/023360 patent/WO2004011536A1/en not_active Ceased
- 2003-07-24 DE DE60304208T patent/DE60304208T2/de not_active Expired - Lifetime
- 2003-07-24 EP EP03771866A patent/EP1490427B1/en not_active Expired - Lifetime
- 2003-07-24 JP JP2005505620A patent/JP5496440B2/ja not_active Expired - Fee Related
- 2003-07-24 MX MXPA04011464A patent/MXPA04011464A/es active IP Right Grant
- 2003-07-24 ES ES03771866T patent/ES2256784T3/es not_active Expired - Lifetime
- 2003-07-24 BR BRPI0311798-7A patent/BR0311798B1/pt not_active IP Right Cessation
- 2003-07-24 CN CNB038177560A patent/CN100419007C/zh not_active Expired - Fee Related
- 2003-07-24 CA CA002492866A patent/CA2492866A1/en not_active Abandoned
-
2013
- 2013-10-30 JP JP2013224965A patent/JP2014051672A/ja not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| KR20050030170A (ko) | 2005-03-29 |
| CN100419007C (zh) | 2008-09-17 |
| ES2256784T3 (es) | 2006-07-16 |
| JP2005533923A (ja) | 2005-11-10 |
| EP1490427B1 (en) | 2006-03-22 |
| BR0311798A (pt) | 2005-03-15 |
| CA2492866A1 (en) | 2004-02-05 |
| MXPA04011464A (es) | 2005-02-14 |
| KR101021533B1 (ko) | 2011-03-16 |
| EP1490427A1 (en) | 2004-12-29 |
| BR0311798B1 (pt) | 2012-12-11 |
| CN1671779A (zh) | 2005-09-21 |
| DE60304208D1 (de) | 2006-05-11 |
| DE60304208T2 (de) | 2007-03-08 |
| WO2004011536A1 (en) | 2004-02-05 |
| JP2014051672A (ja) | 2014-03-20 |
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