JP2012077143A - プライマー組成物 - Google Patents
プライマー組成物 Download PDFInfo
- Publication number
- JP2012077143A JP2012077143A JP2010222040A JP2010222040A JP2012077143A JP 2012077143 A JP2012077143 A JP 2012077143A JP 2010222040 A JP2010222040 A JP 2010222040A JP 2010222040 A JP2010222040 A JP 2010222040A JP 2012077143 A JP2012077143 A JP 2012077143A
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- Prior art keywords
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- polymer
- silane coupling
- Prior art date
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- Granted
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- 239000000203 mixture Substances 0.000 title claims abstract description 113
- 229920000620 organic polymer Polymers 0.000 claims abstract description 79
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims abstract description 71
- 239000006087 Silane Coupling Agent Substances 0.000 claims abstract description 54
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims abstract description 43
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 34
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 28
- 229910000019 calcium carbonate Inorganic materials 0.000 claims abstract description 21
- 125000003277 amino group Chemical group 0.000 claims abstract description 20
- 230000001070 adhesive effect Effects 0.000 claims abstract description 18
- 239000000853 adhesive Substances 0.000 claims abstract description 16
- XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims abstract description 14
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims abstract description 13
- -1 dibutyltin compound Chemical class 0.000 claims description 120
- 229920000642 polymer Polymers 0.000 claims description 73
- 239000004014 plasticizer Substances 0.000 claims description 28
- 239000003054 catalyst Substances 0.000 claims description 23
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 22
- 239000004202 carbamide Substances 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 32
- 239000000463 material Substances 0.000 abstract description 13
- 239000000758 substrate Substances 0.000 abstract description 6
- 239000012790 adhesive layer Substances 0.000 abstract description 4
- 239000003960 organic solvent Substances 0.000 abstract description 2
- 230000002411 adverse Effects 0.000 abstract 1
- 230000002708 enhancing effect Effects 0.000 abstract 1
- 238000007654 immersion Methods 0.000 abstract 1
- 238000000034 method Methods 0.000 description 64
- 150000001875 compounds Chemical class 0.000 description 51
- 239000000047 product Substances 0.000 description 41
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 32
- 239000003822 epoxy resin Substances 0.000 description 31
- 229920000647 polyepoxide Polymers 0.000 description 31
- 238000001723 curing Methods 0.000 description 27
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 23
- 229920001577 copolymer Polymers 0.000 description 19
- 230000000694 effects Effects 0.000 description 17
- 229920005989 resin Polymers 0.000 description 17
- 239000011347 resin Substances 0.000 description 17
- 150000002430 hydrocarbons Chemical group 0.000 description 16
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 16
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 15
- 229920005862 polyol Polymers 0.000 description 14
- 150000003077 polyols Chemical class 0.000 description 14
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 13
- 239000007795 chemical reaction product Substances 0.000 description 13
- 239000003795 chemical substances by application Substances 0.000 description 12
- 239000000945 filler Substances 0.000 description 12
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 12
- 229920001451 polypropylene glycol Polymers 0.000 description 12
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 11
- 238000002156 mixing Methods 0.000 description 11
- 229920000570 polyether Polymers 0.000 description 11
- 229910000077 silane Inorganic materials 0.000 description 11
- 239000002904 solvent Substances 0.000 description 11
- 238000003860 storage Methods 0.000 description 11
- 229920002554 vinyl polymer Polymers 0.000 description 11
- SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 description 10
- 239000002585 base Substances 0.000 description 10
- 238000004519 manufacturing process Methods 0.000 description 10
- 238000010526 radical polymerization reaction Methods 0.000 description 10
- 150000004756 silanes Chemical class 0.000 description 10
- 229910052710 silicon Inorganic materials 0.000 description 10
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 239000002253 acid Substances 0.000 description 9
- 239000003963 antioxidant agent Substances 0.000 description 9
- 238000009826 distribution Methods 0.000 description 9
- 150000002148 esters Chemical class 0.000 description 9
- 239000004611 light stabiliser Substances 0.000 description 9
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 9
- 230000035699 permeability Effects 0.000 description 9
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 8
- IJKVHSBPTUYDLN-UHFFFAOYSA-N dihydroxy(oxo)silane Chemical compound O[Si](O)=O IJKVHSBPTUYDLN-UHFFFAOYSA-N 0.000 description 8
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical group CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 8
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 8
- 125000003396 thiol group Chemical group [H]S* 0.000 description 8
- LVACOMKKELLCHJ-UHFFFAOYSA-N 3-trimethoxysilylpropylurea Chemical compound CO[Si](OC)(OC)CCCNC(N)=O LVACOMKKELLCHJ-UHFFFAOYSA-N 0.000 description 7
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 7
- 125000003118 aryl group Chemical group 0.000 description 7
- XITRBUPOXXBIJN-UHFFFAOYSA-N bis(2,2,6,6-tetramethylpiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)NC(C)(C)C1 XITRBUPOXXBIJN-UHFFFAOYSA-N 0.000 description 7
- 230000018044 dehydration Effects 0.000 description 7
- 238000006297 dehydration reaction Methods 0.000 description 7
- 239000003063 flame retardant Substances 0.000 description 7
- 125000000524 functional group Chemical group 0.000 description 7
- 229930195733 hydrocarbon Natural products 0.000 description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 7
- 125000000962 organic group Chemical group 0.000 description 7
- 239000005011 phenolic resin Substances 0.000 description 7
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 6
- 239000004593 Epoxy Substances 0.000 description 6
- 239000004721 Polyphenylene oxide Substances 0.000 description 6
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 6
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 6
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 6
- 125000002947 alkylene group Chemical group 0.000 description 6
- 150000001408 amides Chemical class 0.000 description 6
- 230000003078 antioxidant effect Effects 0.000 description 6
- 238000013329 compounding Methods 0.000 description 6
- AYOHIQLKSOJJQH-UHFFFAOYSA-N dibutyltin Chemical compound CCCC[Sn]CCCC AYOHIQLKSOJJQH-UHFFFAOYSA-N 0.000 description 6
- 235000014113 dietary fatty acids Nutrition 0.000 description 6
- 125000003700 epoxy group Chemical group 0.000 description 6
- 239000000194 fatty acid Substances 0.000 description 6
- 229930195729 fatty acid Natural products 0.000 description 6
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 6
- 238000006460 hydrolysis reaction Methods 0.000 description 6
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 6
- 229920001228 polyisocyanate Polymers 0.000 description 6
- 239000005056 polyisocyanate Substances 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 6
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 5
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 5
- OSDWBNJEKMUWAV-UHFFFAOYSA-N Allyl chloride Chemical compound ClCC=C OSDWBNJEKMUWAV-UHFFFAOYSA-N 0.000 description 5
- 239000004215 Carbon black (E152) Substances 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- 239000004793 Polystyrene Substances 0.000 description 5
- 150000001412 amines Chemical class 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 5
- LQRUPWUPINJLMU-UHFFFAOYSA-N dioctyl(oxo)tin Chemical compound CCCCCCCC[Sn](=O)CCCCCCCC LQRUPWUPINJLMU-UHFFFAOYSA-N 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
- 150000004665 fatty acids Chemical class 0.000 description 5
- 230000009477 glass transition Effects 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 239000003999 initiator Substances 0.000 description 5
- 239000012948 isocyanate Substances 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 238000006116 polymerization reaction Methods 0.000 description 5
- 229920002223 polystyrene Polymers 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 5
- 235000012239 silicon dioxide Nutrition 0.000 description 5
- 229920006132 styrene block copolymer Polymers 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 5
- PZJJKWKADRNWSW-UHFFFAOYSA-N trimethoxysilicon Chemical group CO[Si](OC)OC PZJJKWKADRNWSW-UHFFFAOYSA-N 0.000 description 5
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 5
- GQHTUMJGOHRCHB-UHFFFAOYSA-N 2,3,4,6,7,8,9,10-octahydropyrimido[1,2-a]azepine Chemical compound C1CCCCN2CCCN=C21 GQHTUMJGOHRCHB-UHFFFAOYSA-N 0.000 description 4
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 4
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 4
- UUEWCQRISZBELL-UHFFFAOYSA-N 3-trimethoxysilylpropane-1-thiol Chemical compound CO[Si](OC)(OC)CCCS UUEWCQRISZBELL-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 125000003368 amide group Chemical group 0.000 description 4
- 238000010560 atom transfer radical polymerization reaction Methods 0.000 description 4
- 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 4
- 150000001728 carbonyl compounds Chemical class 0.000 description 4
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- 230000000052 comparative effect Effects 0.000 description 4
- 239000003085 diluting agent Substances 0.000 description 4
- PKTOVQRKCNPVKY-UHFFFAOYSA-N dimethoxy(methyl)silicon Chemical compound CO[Si](C)OC PKTOVQRKCNPVKY-UHFFFAOYSA-N 0.000 description 4
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- 229920002647 polyamide Polymers 0.000 description 4
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- FMGBDYLOANULLW-UHFFFAOYSA-N 3-isocyanatopropyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)CCCN=C=O FMGBDYLOANULLW-UHFFFAOYSA-N 0.000 description 3
- LVNLBBGBASVLLI-UHFFFAOYSA-N 3-triethoxysilylpropylurea Chemical compound CCO[Si](OCC)(OCC)CCCNC(N)=O LVNLBBGBASVLLI-UHFFFAOYSA-N 0.000 description 3
- 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 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
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- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 3
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- 239000004952 Polyamide Substances 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 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 3
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- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 3
- 239000001361 adipic acid Substances 0.000 description 3
- 235000011037 adipic acid Nutrition 0.000 description 3
- 125000003342 alkenyl group Chemical group 0.000 description 3
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 3
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 3
- 239000012964 benzotriazole Substances 0.000 description 3
- RRDGKBOYQLLJSW-UHFFFAOYSA-N bis(2-ethylhexyl) 7-oxabicyclo[4.1.0]heptane-3,4-dicarboxylate Chemical compound C1C(C(=O)OCC(CC)CCCC)C(C(=O)OCC(CC)CCCC)CC2OC21 RRDGKBOYQLLJSW-UHFFFAOYSA-N 0.000 description 3
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N butyric aldehyde Natural products CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 3
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 239000007822 coupling agent Substances 0.000 description 3
- JGFBRKRYDCGYKD-UHFFFAOYSA-N dibutyl(oxo)tin Chemical compound CCCC[Sn](=O)CCCC JGFBRKRYDCGYKD-UHFFFAOYSA-N 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- HGQSXVKHVMGQRG-UHFFFAOYSA-N dioctyltin Chemical compound CCCCCCCC[Sn]CCCCCCCC HGQSXVKHVMGQRG-UHFFFAOYSA-N 0.000 description 3
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
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- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 3
- PHQOGHDTIVQXHL-UHFFFAOYSA-N n'-(3-trimethoxysilylpropyl)ethane-1,2-diamine Chemical compound CO[Si](OC)(OC)CCCNCCN PHQOGHDTIVQXHL-UHFFFAOYSA-N 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 3
- 239000003973 paint Substances 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 150000003141 primary amines Chemical class 0.000 description 3
- 150000003254 radicals Chemical class 0.000 description 3
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- 239000005060 rubber Substances 0.000 description 3
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 238000004381 surface treatment Methods 0.000 description 3
- 238000001308 synthesis method Methods 0.000 description 3
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
- LFQCEHFDDXELDD-UHFFFAOYSA-N tetramethyl orthosilicate Chemical compound CO[Si](OC)(OC)OC LFQCEHFDDXELDD-UHFFFAOYSA-N 0.000 description 3
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 3
- NMEPHPOFYLLFTK-UHFFFAOYSA-N trimethoxy(octyl)silane Chemical compound CCCCCCCC[Si](OC)(OC)OC NMEPHPOFYLLFTK-UHFFFAOYSA-N 0.000 description 3
- YUYCVXFAYWRXLS-UHFFFAOYSA-N trimethoxysilane Chemical compound CO[SiH](OC)OC YUYCVXFAYWRXLS-UHFFFAOYSA-N 0.000 description 3
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 2
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- DQZNLOXENNXVAD-UHFFFAOYSA-N trimethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OC)(OC)OC)CCC2OC21 DQZNLOXENNXVAD-UHFFFAOYSA-N 0.000 description 1
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- ARKBFSWVHXKMSD-UHFFFAOYSA-N trimethoxysilylmethanamine Chemical compound CO[Si](CN)(OC)OC ARKBFSWVHXKMSD-UHFFFAOYSA-N 0.000 description 1
- UOKUUKOEIMCYAI-UHFFFAOYSA-N trimethoxysilylmethyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)COC(=O)C(C)=C UOKUUKOEIMCYAI-UHFFFAOYSA-N 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
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- MBYLVOKEDDQJDY-UHFFFAOYSA-N tris(2-aminoethyl)amine Chemical compound NCCN(CCN)CCN MBYLVOKEDDQJDY-UHFFFAOYSA-N 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 235000021081 unsaturated fats Nutrition 0.000 description 1
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- KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 1
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- 239000004711 α-olefin Substances 0.000 description 1
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Abstract
【解決手段】(A)反応性ケイ素基を有する有機重合体、(B)重質炭酸カルシウム、(C)アミノ基含有シランカップリング剤、(D)ウレタン基および/またはウレア基を有するシランカップリング剤、および/または(E)炭素数が8以上のアルキル基を有するシランカップリング剤、を含有するプライマー組成物。
【選択図】図1
Description
すなわち本発明は、
1).(A)シロキサン結合を形成することにより架橋し得るケイ素基を有する有機重合体、(B)重質炭酸カルシウム、(C)アミノ基を有するシランカップリング剤、(D)ウレタン基および/またはウレア基を有するシランカップリング剤、を含むプライマー組成物に関する。
2).(A)シロキサン結合を形成することにより架橋し得るケイ素基を有する有機重合体、(B)重質炭酸カルシウム、(C)アミノ基を有するシランカップリング剤、(E)炭素数が8以上の長鎖アルキル基を有するシランカップリング剤、を含むプライマー組成物に関する。
3).有機重合体(A)の主鎖骨格が、ポリオキシアルキレン系重合体および/または(メタ)アクリル酸エステル系重合体であるプライマー組成物に関する。
4).硬化性組成物中に含まれるジブチル錫化合物の含有率が0.3重量%以下であるプライマー組成物に関する。
5).硬化性組成物中に含まれる硬化触媒が、ジオクチル錫化合物であるプライマー組成物に関する。
6).硬化性組成物中に含まれる可塑剤の含有率が15重量%以下であるプライマー組成物に関する。
7).コンクリート下地に施工されるプライマー組成物に関する。
8).コンクリート下地と、床用接着剤の間に用いられるプライマー組成物に関する。
−SiR1 3−aXa (1)
((3−a)個のR1はそれぞれ独立に炭素原子数1〜20のアルキル基、炭素原子数6〜20のアリール基、炭素原子数7〜20のアラルキル基、および、−OSi(R’)3(R’は、それぞれ独立に炭素原子数1〜20の炭化水素基である。)で示されるトリオルガノシロキシ基からなる群より選択される少なくとも1つである。a個のXはそれぞれ独立に水酸基または加水分解性基のいずれかである。また、aは1〜3の整数である。)で示される基があげられる。
H−(SiR2 2O)nSiR2 2−R3−SiX3 (2)
(3個のXは一般式(1)の表記と同じ。(2n+2)個のR2はそれぞれ独立に炭化水素基である。R3は2価の有機基である。また、nは0〜19の整数である。)で示されるシラン化合物は、不均化反応が進まない。このため、(イ)の合成法で、1つのケイ素原子に3個の加水分解性基が結合している基を導入する場合には、一般式(2)で示されるシラン化合物を用いることが好ましい。
−R4−O− (3)
(R4は炭素原子数1〜14の直鎖状もしくは分岐状アルキレン基である。)で表される繰り返し単位を有する重合体である。
−CH2O−、−CH2CH2O−、−CH2CH(CH3)O−、−CH2CH(C2H5)O−、−CH2C(CH3)2O−、−CH2CH2CH2CH2O−
などがあげられる。
−CH2−C(R5)(COOR6)− (4)
(R5は水素原子またはメチル基、R6は炭素原子数1〜8のアルキル基である。)で示される炭素原子数1〜8のアルキル基を有する繰り返し単位と、
一般式(5):
−CH2−C(R5)(COOR7)− (5)
(R5は一般式(4)の表記と同じ。R7は炭素原子数9以上のアルキル基である。)で示される炭素原子数9以上のアルキル基を有する繰り返し単位とからなる共重合体があげられる。
−NR8−C(=O)− (6)
(R8は水素原子または有機基である。)で示される有機基をいう。
W−R9−SiR1 3−aXa (7)
(R1、X、aは一般式(1)の表記と同じ。R9は2価の有機基であり、より好ましくは炭素原子数1〜20の2価の炭化水素基である。Wは水酸基、カルボキシル基、メルカプト基およびアミノ基(1級または2級)からなる群より選択される、少なくとも1つの活性水素を有する基である。)で示されるケイ素化合物中のWを反応させる方法があげられる。
O=C=N−R9−SiR1 3−aXa (8)
(R9、R1、X、aは一般式(1)および一般式(7)の表記と同じ。)で示される反応性ケイ素基を有するイソシアネート化合物のイソシアネート基を反応させる方法があげられる。
(C)アミノ基含有シランカップリング剤と、シランカップリング剤(D)の配合量の合計は、5〜25重量部であるのが好ましく、10〜20重量部であるのが特に好ましい。
(C)アミノ基含有シランカップリング剤と、シランカップリング剤(E)の配合量の合計は、5〜25重量部であるのが好ましく、10〜20重量部であるのが特に好ましい。
本発明のプライマー組成物は低粘度、無溶剤、かつ接着性が良好であることからコーティング材やプライマーとして好適に使用することが可能である。特に、内装用でコンクリート下地と床用接着剤との接着性を改善するプライマーとして有用である。
分子量約3,000のポリオキシプロピレンジオールの水酸基に対して1.2倍当量のNaOMeのメタノール溶液を添加してメタノールを留去し、さらに塩化アリルを添加して末端の水酸基をアリル基に変換した。未反応の塩化アリルは減圧脱揮により除去した。得られた未精製のアリル末端ポリプロピレンオキシド100重量部に対し、n−ヘキサン300重量部と、水300重量部を混合攪拌した後、遠心分離により水を除去し、得られたヘキサン溶液にさらに水300重量部を混合攪拌し、再度遠心分離により水を除去した後、ヘキサンを減圧脱揮により除去した。
分子量約3,000のポリオキシプロピレントリオールを開始剤とし、亜鉛ヘキサシアノコバルテートグライム錯体触媒にてプロピレンオキシドの重合を行い、数平均分子量16,400(送液システムとして東ソー製HLC−8120GPCを用い、カラムは東ソー製TSK−GEL Hタイプを用い、溶媒はTHFを用いて測定したポリスチレン換算分子量)のポリプロピレンオキシドを得た。続いて、この水酸基末端ポリプロピレンオキシドの水酸基に対して1.2倍当量のNaOMeのメタノール溶液を添加してメタノールを留去し、さらに塩化アリルを添加して末端の水酸基をアリル基に変換した。未反応の塩化アリルは減圧脱揮により除去した。得られた未精製のアリル末端ポリプロピレンオキシド100重量部に対し、n−ヘキサン300重量部と、水300重量部を混合攪拌した後、遠心分離により水を除去し、得られたヘキサン溶液にさらに水300重量部を混合攪拌し、再度遠心分離により水を除去した後、ヘキサンを減圧脱揮により除去した。
合成例1で得られた反応性ケイ素基を有する有機重合体(A−1)を100重量部に対して、重質炭酸カルシウム(Imerys社製、商品名:Carbital 110)135重量部を計量し、よく分散・混合した。これに、テトラエチルシリケート(Evonik社製、商品名:Dynasylan A)7重量部、アミノプロピルトリメトキシシラン(Evonik社製、商品名:Dynasylan AMMO)7重量部、ウレイドプロピルトリメトキシシラン(Momentive社製、商品名:SILQUEST A−1524 Silane)、ビニルトリメトキシシラン(Evonik社製、商品名:Dynasylan VTMO)2重量部、硬化触媒としてジオクチル錫オキサイドとエチルシリケートの混合物(日東化成(株)製、商品名:ネオスタンS−1)1重量部を計量し、自転・公転ミキサー((株)シンキー製、商品名:あわとり練太郎)を用いて混合することにより、プライマー組成物を得た。
実施例1におけるウレイドプロピルトリメトキシシランの代わりに、n−オクチルトリメトキシシラン(Evonik社製、商品名:Dynasylan OCTMO)7重量部を用いた以外は、実施例1と同様の方法でプライマー組成物を得た。
実施例1におけるウレイドプロピルトリメトキシシランを用いないこと以外は、実施例1と同様の方法でプライマー組成物を得た。
実施例1におけるテトラエチルシリケートの使用量を12.5重量部に、アミノプロピルトリメトキシシランの使用量を12.5重量部にそれぞれ変更し、かつウレイドプロピルトリメトキシシランを用いないこと以外は、実施例1と同様の方法でプライマー組成物を得た。
23℃、50%RH条件下にて上記プライマー組成物を厚みが約3mmになるよう伸ばし、ミクロスパテュラを用いて経時でプライマー組成物の表面に軽く触れ、組成物がミクロスパテュラについてこなくなるまでの時間を測定した。
23℃、50%RH条件下にて上記プライマー組成物を約2mm厚の薄層シート状に成型し、7日間硬化養生した。内部に水を入れたガラス容器の上部にこの薄層シートを密着させ、23℃条件下でのデシケータ内に設置した。デシケータの底部には乾燥させたシリカゲルを十分量入れた。評価方法の概略を図1に示す。初期と、1週間後、4週間後、12週間後のそれぞれのカップ全体の重量を測定し、減量した値を表1に記載した。減量した数値は、硬化した薄膜を水蒸気が透過した量とみなした。
上記プライマー組成物をコンクリート基材上に約2mmの厚みで塗布し、23℃、50%RH条件下で24時間硬化養生した。その後、下記の床用接着剤をビード状に塗布し、同条件で7日間硬化養生を行った。このビード状の硬化物に切り込みを入れ、引っ張ることにより接着性を評価した。また、別のビード状硬化物を水に浸水し、7日間漬けた後、同様に硬化物に切り込みを入れて引っ張ることにより接着性を評価した。接着状態は、接着剤層が凝集破壊の場合はC、界面破壊の場合はAと記し、凝集破壊の方が接着状態は良好なことを示す。凝集破壊と界面破壊が混合した状態になった場合は、それぞれの割合を数値で示し、合計が100になるようにした。すなわち、C50A50は、凝集破壊が50%、界面破壊が50%の状態を表す。
Claims (8)
- (A)シロキサン結合を形成することにより架橋し得るケイ素基を有する有機重合体、(B)重質炭酸カルシウム、(C)アミノ基を有するシランカップリング剤、(D)ウレタン基および/またはウレア基を有するシランカップリング剤、を含むプライマー組成物。
- (A)シロキサン結合を形成することにより架橋し得るケイ素基を有する有機重合体、(B)重質炭酸カルシウム、(C)アミノ基を有するシランカップリング剤、(E)炭素数が8以上の長鎖アルキル基を有するシランカップリング剤、を含むプライマー組成物。
- 有機重合体(A)の主鎖骨格が、ポリオキシアルキレン系重合体および/または(メタ)アクリル酸エステル系重合体である、請求項1または請求項2のいずれかに記載のプライマー組成物。
- 硬化性組成物中に含まれるジブチル錫化合物の含有率が0.3重量%以下である、請求項1から請求項3のいずれかに記載のプライマー組成物。
- 硬化性組成物中に含まれる硬化触媒が、ジオクチル錫化合物である、請求項1から請求項4のいずれかに記載のプライマー組成物。
- 硬化性組成物中に含まれる可塑剤の含有率が15重量%以下である、請求項1から請求項5のいずれかに記載のプライマー組成物。
- コンクリート下地に施工される、請求項6に記載のプライマー組成物。
- コンクリート下地と、床用接着剤の間に用いられることを特徴とする請求項7に記載のプライマー組成物。
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103509501A (zh) * | 2012-06-28 | 2014-01-15 | 施敏打硬株式会社 | 固化性组合物和固化催化剂 |
JP2017145355A (ja) * | 2016-02-19 | 2017-08-24 | 大日本塗料株式会社 | 2液型水系下塗り塗料組成物、塗装体及びその製造方法 |
JP2019502569A (ja) * | 2015-11-11 | 2019-01-31 | クナウフ ギプス カーゲー | 断熱体を含む多層層状体 |
CN112646462A (zh) * | 2020-12-16 | 2021-04-13 | 大禹伟业(北京)国际科技有限公司 | 一种硅烷改性聚醚密封胶的专用底涂及其制备方法和应用 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001323210A (ja) * | 2000-03-08 | 2001-11-22 | Kanegafuchi Chem Ind Co Ltd | プライマー組成物および接着方法 |
JP2007277311A (ja) * | 2006-04-03 | 2007-10-25 | Kaneka Corp | プライマー組成物 |
JP2010132727A (ja) * | 2008-12-02 | 2010-06-17 | Kaneka Corp | 硬化性組成物と硬化物 |
JP2013509476A (ja) * | 2009-10-30 | 2013-03-14 | ヘンケル・アクチェンゲゼルシャフト・ウント・コムパニー・コマンディットゲゼルシャフト・アウフ・アクチェン | シーラントおよび接着剤において使用するための尿素結合型アルコキシシラン |
-
2010
- 2010-09-30 JP JP2010222040A patent/JP5584575B2/ja active Active
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001323210A (ja) * | 2000-03-08 | 2001-11-22 | Kanegafuchi Chem Ind Co Ltd | プライマー組成物および接着方法 |
JP2007277311A (ja) * | 2006-04-03 | 2007-10-25 | Kaneka Corp | プライマー組成物 |
JP2010132727A (ja) * | 2008-12-02 | 2010-06-17 | Kaneka Corp | 硬化性組成物と硬化物 |
JP2013509476A (ja) * | 2009-10-30 | 2013-03-14 | ヘンケル・アクチェンゲゼルシャフト・ウント・コムパニー・コマンディットゲゼルシャフト・アウフ・アクチェン | シーラントおよび接着剤において使用するための尿素結合型アルコキシシラン |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103509501A (zh) * | 2012-06-28 | 2014-01-15 | 施敏打硬株式会社 | 固化性组合物和固化催化剂 |
JP2019502569A (ja) * | 2015-11-11 | 2019-01-31 | クナウフ ギプス カーゲー | 断熱体を含む多層層状体 |
US10947723B2 (en) | 2015-11-11 | 2021-03-16 | Knauf Gips Kg | Multilayered layered body comprising a thermal insulation body |
JP2017145355A (ja) * | 2016-02-19 | 2017-08-24 | 大日本塗料株式会社 | 2液型水系下塗り塗料組成物、塗装体及びその製造方法 |
CN112646462A (zh) * | 2020-12-16 | 2021-04-13 | 大禹伟业(北京)国际科技有限公司 | 一种硅烷改性聚醚密封胶的专用底涂及其制备方法和应用 |
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