JP4563936B2 - 硬化性組成物 - Google Patents
硬化性組成物 Download PDFInfo
- Publication number
- JP4563936B2 JP4563936B2 JP2005505259A JP2005505259A JP4563936B2 JP 4563936 B2 JP4563936 B2 JP 4563936B2 JP 2005505259 A JP2005505259 A JP 2005505259A JP 2005505259 A JP2005505259 A JP 2005505259A JP 4563936 B2 JP4563936 B2 JP 4563936B2
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- 239000000203 mixture Substances 0.000 title claims abstract description 82
- 229920000642 polymer Polymers 0.000 claims abstract description 171
- -1 polyoxypropylene Polymers 0.000 claims abstract description 141
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims abstract description 80
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims abstract description 38
- 229920001451 polypropylene glycol Polymers 0.000 claims abstract description 32
- 239000000178 monomer Substances 0.000 claims description 51
- 238000010526 radical polymerization reaction Methods 0.000 claims description 21
- 238000009826 distribution Methods 0.000 claims description 15
- 238000010560 atom transfer radical polymerization reaction Methods 0.000 claims description 13
- 230000000379 polymerizing effect Effects 0.000 claims description 6
- 125000004492 methyl ester group Chemical group 0.000 claims description 5
- 238000003860 storage Methods 0.000 abstract description 12
- 239000003566 sealing material Substances 0.000 abstract description 9
- 229920006222 acrylic ester polymer Polymers 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 description 74
- 238000000034 method Methods 0.000 description 71
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 49
- 239000000047 product Substances 0.000 description 48
- 239000003054 catalyst Substances 0.000 description 43
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 42
- 125000003342 alkenyl group Chemical group 0.000 description 42
- 239000000126 substance Substances 0.000 description 39
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 36
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 34
- 229910052736 halogen Inorganic materials 0.000 description 34
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 33
- 125000004432 carbon atom Chemical group C* 0.000 description 29
- 229920002554 vinyl polymer Polymers 0.000 description 29
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- 238000006243 chemical reaction Methods 0.000 description 27
- 230000000694 effects Effects 0.000 description 27
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- 238000003786 synthesis reaction Methods 0.000 description 23
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- 150000004820 halides Chemical class 0.000 description 18
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- 229910052751 metal Inorganic materials 0.000 description 15
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- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 15
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- 125000000524 functional group Chemical group 0.000 description 12
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- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 12
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 11
- 229910020175 SiOH Inorganic materials 0.000 description 11
- 150000001412 amines Chemical class 0.000 description 11
- 125000003277 amino group Chemical group 0.000 description 11
- 125000003118 aryl group Chemical group 0.000 description 11
- 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 11
- 238000005259 measurement Methods 0.000 description 11
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- 239000000377 silicon dioxide Substances 0.000 description 11
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- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 10
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- 229910052723 transition metal Inorganic materials 0.000 description 10
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 9
- 125000003710 aryl alkyl group Chemical group 0.000 description 9
- 235000014113 dietary fatty acids Nutrition 0.000 description 9
- 239000000194 fatty acid Substances 0.000 description 9
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- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 9
- 229910052710 silicon Inorganic materials 0.000 description 9
- 150000003624 transition metals Chemical class 0.000 description 9
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 8
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 8
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 8
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- 239000004593 Epoxy Substances 0.000 description 7
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- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 7
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- 239000011521 glass Substances 0.000 description 7
- 239000001257 hydrogen Substances 0.000 description 7
- 229910052739 hydrogen Inorganic materials 0.000 description 7
- 239000012948 isocyanate Substances 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 7
- 125000000962 organic group Chemical group 0.000 description 7
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 7
- 229920000570 polyether Polymers 0.000 description 7
- 229920005862 polyol Polymers 0.000 description 7
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- 239000000843 powder Substances 0.000 description 7
- 238000007665 sagging Methods 0.000 description 7
- 235000012239 silicon dioxide Nutrition 0.000 description 7
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 6
- 239000004721 Polyphenylene oxide Substances 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 6
- 230000002378 acidificating effect Effects 0.000 description 6
- 230000001070 adhesive effect Effects 0.000 description 6
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 6
- 229910052782 aluminium Inorganic materials 0.000 description 6
- KBPLFHHGFOOTCA-UHFFFAOYSA-N caprylic alcohol Natural products CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 6
- 238000013329 compounding Methods 0.000 description 6
- 238000004132 cross linking Methods 0.000 description 6
- 230000009257 reactivity Effects 0.000 description 6
- 150000004756 silanes Chemical class 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 5
- 239000000654 additive Substances 0.000 description 5
- 125000003368 amide group Chemical group 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- 239000004927 clay Substances 0.000 description 5
- 150000001993 dienes Chemical class 0.000 description 5
- 125000006575 electron-withdrawing group Chemical group 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 5
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 5
- 239000003607 modifier Substances 0.000 description 5
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 5
- 150000003254 radicals Chemical class 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 150000003377 silicon compounds Chemical class 0.000 description 5
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 5
- XWJBRBSPAODJER-UHFFFAOYSA-N 1,7-octadiene Chemical compound C=CCCCCC=C XWJBRBSPAODJER-UHFFFAOYSA-N 0.000 description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 4
- SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 description 4
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 4
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 4
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-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
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 4
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- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
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- 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
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- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 4
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- UKODFQOELJFMII-UHFFFAOYSA-N pentamethyldiethylenetriamine Chemical compound CN(C)CCN(C)CCN(C)C UKODFQOELJFMII-UHFFFAOYSA-N 0.000 description 4
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- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 4
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- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 description 3
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- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 3
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- 230000015556 catabolic process Effects 0.000 description 3
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- 125000001309 chloro group Chemical group Cl* 0.000 description 3
- 239000010941 cobalt Substances 0.000 description 3
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- 239000003086 colorant Substances 0.000 description 3
- NKNDPYCGAZPOFS-UHFFFAOYSA-M copper(i) bromide Chemical compound Br[Cu] NKNDPYCGAZPOFS-UHFFFAOYSA-M 0.000 description 3
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- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 1
- XTAZYLNFDRKIHJ-UHFFFAOYSA-N n,n-dioctyloctan-1-amine Chemical compound CCCCCCCCN(CCCCCCCC)CCCCCCCC XTAZYLNFDRKIHJ-UHFFFAOYSA-N 0.000 description 1
- OOHAUGDGCWURIT-UHFFFAOYSA-N n,n-dipentylpentan-1-amine Chemical compound CCCCCN(CCCCC)CCCCC OOHAUGDGCWURIT-UHFFFAOYSA-N 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- CLYWMXVFAMGARU-UHFFFAOYSA-N n-benzyl-3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCNCC1=CC=CC=C1 CLYWMXVFAMGARU-UHFFFAOYSA-N 0.000 description 1
- WIBFFTLQMKKBLZ-SEYXRHQNSA-N n-butyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCCCC WIBFFTLQMKKBLZ-SEYXRHQNSA-N 0.000 description 1
- GMTCPFCMAHMEMT-UHFFFAOYSA-N n-decyldecan-1-amine Chemical compound CCCCCCCCCCNCCCCCCCCCC GMTCPFCMAHMEMT-UHFFFAOYSA-N 0.000 description 1
- LQKYCMRSWKQVBQ-UHFFFAOYSA-N n-dodecylaniline Chemical compound CCCCCCCCCCCCNC1=CC=CC=C1 LQKYCMRSWKQVBQ-UHFFFAOYSA-N 0.000 description 1
- 125000003136 n-heptyl 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])* 0.000 description 1
- NQYKSVOHDVVDOR-UHFFFAOYSA-N n-hexadecylhexadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCNCCCCCCCCCCCCCCCC NQYKSVOHDVVDOR-UHFFFAOYSA-N 0.000 description 1
- SZEGKVHRCLBFKJ-UHFFFAOYSA-N n-methyloctadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCNC SZEGKVHRCLBFKJ-UHFFFAOYSA-N 0.000 description 1
- UEKWTIYPDJLSKK-UHFFFAOYSA-N n-octadecylaniline Chemical compound CCCCCCCCCCCCCCCCCCNC1=CC=CC=C1 UEKWTIYPDJLSKK-UHFFFAOYSA-N 0.000 description 1
- HKUFIYBZNQSHQS-UHFFFAOYSA-N n-octadecyloctadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCNCCCCCCCCCCCCCCCCCC HKUFIYBZNQSHQS-UHFFFAOYSA-N 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- JACMPVXHEARCBO-UHFFFAOYSA-N n-pentylpentan-1-amine Chemical compound CCCCCNCCCCC JACMPVXHEARCBO-UHFFFAOYSA-N 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 229910000480 nickel oxide Inorganic materials 0.000 description 1
- PPFQMADUQXIJLH-UHFFFAOYSA-N nickel;tributylphosphane Chemical compound [Ni].CCCCP(CCCC)CCCC.CCCCP(CCCC)CCCC PPFQMADUQXIJLH-UHFFFAOYSA-N 0.000 description 1
- UYLRKRLDQUXYKB-UHFFFAOYSA-N nickel;triphenylphosphane Chemical compound [Ni].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 UYLRKRLDQUXYKB-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- FJDUDHYHRVPMJZ-UHFFFAOYSA-N nonan-1-amine Chemical compound CCCCCCCCCN FJDUDHYHRVPMJZ-UHFFFAOYSA-N 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- QUAMTGJKVDWJEQ-UHFFFAOYSA-N octabenzone Chemical compound OC1=CC(OCCCCCCCC)=CC=C1C(=O)C1=CC=CC=C1 QUAMTGJKVDWJEQ-UHFFFAOYSA-N 0.000 description 1
- JFOJYGMDZRCSPA-UHFFFAOYSA-J octadecanoate;tin(4+) Chemical compound [Sn+4].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O JFOJYGMDZRCSPA-UHFFFAOYSA-J 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 description 1
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 description 1
- 229960002446 octanoic acid Drugs 0.000 description 1
- ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 description 1
- ZMHZSHHZIKJFIR-UHFFFAOYSA-N octyltin Chemical class CCCCCCCC[Sn] ZMHZSHHZIKJFIR-UHFFFAOYSA-N 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 150000001282 organosilanes Chemical class 0.000 description 1
- 150000003961 organosilicon compounds Chemical class 0.000 description 1
- GNRSAWUEBMWBQH-UHFFFAOYSA-N oxonickel Chemical compound [Ni]=O GNRSAWUEBMWBQH-UHFFFAOYSA-N 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 125000000913 palmityl 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])[H] 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- DPBLXKKOBLCELK-UHFFFAOYSA-N pentan-1-amine Chemical compound CCCCCN DPBLXKKOBLCELK-UHFFFAOYSA-N 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 239000010451 perlite Substances 0.000 description 1
- 235000019362 perlite Nutrition 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 150000004980 phosphorus peroxides Chemical class 0.000 description 1
- PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 description 1
- 150000003058 platinum compounds Chemical class 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920002589 poly(vinylethylene) polymer Polymers 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 150000007519 polyprotic acids Polymers 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- 150000004032 porphyrins Chemical class 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 238000004382 potting Methods 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 239000010734 process oil Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- HKJYVRJHDIPMQB-UHFFFAOYSA-N propan-1-olate;titanium(4+) Chemical compound CCCO[Ti](OCCC)(OCCC)OCCC HKJYVRJHDIPMQB-UHFFFAOYSA-N 0.000 description 1
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 238000007348 radical reaction Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 238000007151 ring opening polymerisation reaction Methods 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 150000003304 ruthenium compounds Chemical class 0.000 description 1
- YBCAZPLXEGKKFM-UHFFFAOYSA-K ruthenium(iii) chloride Chemical compound [Cl-].[Cl-].[Cl-].[Ru+3] YBCAZPLXEGKKFM-UHFFFAOYSA-K 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 150000003461 sulfonyl halides Chemical class 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 125000005425 toluyl group Chemical group 0.000 description 1
- 150000003623 transition metal compounds Chemical class 0.000 description 1
- VPYJNCGUESNPMV-UHFFFAOYSA-N triallylamine Chemical compound C=CCN(CC=C)CC=C VPYJNCGUESNPMV-UHFFFAOYSA-N 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
- YLGRTLMDMVAFNI-UHFFFAOYSA-N tributyl(prop-2-enyl)stannane Chemical compound CCCC[Sn](CCCC)(CCCC)CC=C YLGRTLMDMVAFNI-UHFFFAOYSA-N 0.000 description 1
- 229960001124 trientine Drugs 0.000 description 1
- FRGPKMWIYVTFIQ-UHFFFAOYSA-N triethoxy(3-isocyanatopropyl)silane Chemical compound CCO[Si](OCC)(OCC)CCCN=C=O FRGPKMWIYVTFIQ-UHFFFAOYSA-N 0.000 description 1
- UDUKMRHNZZLJRB-UHFFFAOYSA-N triethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OCC)(OCC)OCC)CCC2OC21 UDUKMRHNZZLJRB-UHFFFAOYSA-N 0.000 description 1
- JXUKBNICSRJFAP-UHFFFAOYSA-N triethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCOCC1CO1 JXUKBNICSRJFAP-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical class OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 1
- ZNOCGWVLWPVKAO-UHFFFAOYSA-N trimethoxy(phenyl)silane Chemical compound CO[Si](OC)(OC)C1=CC=CC=C1 ZNOCGWVLWPVKAO-UHFFFAOYSA-N 0.000 description 1
- HQYALQRYBUJWDH-UHFFFAOYSA-N trimethoxy(propyl)silane Chemical compound CCC[Si](OC)(OC)OC HQYALQRYBUJWDH-UHFFFAOYSA-N 0.000 description 1
- PZJJKWKADRNWSW-UHFFFAOYSA-N trimethoxysilicon Chemical group CO[Si](OC)OC PZJJKWKADRNWSW-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
- ODHXBMXNKOYIBV-UHFFFAOYSA-N triphenylamine Chemical compound C1=CC=CC=C1N(C=1C=CC=CC=1)C1=CC=CC=C1 ODHXBMXNKOYIBV-UHFFFAOYSA-N 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 239000002383 tung oil Substances 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
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 1
- 235000020234 walnut Nutrition 0.000 description 1
- 238000003809 water extraction Methods 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000011667 zinc carbonate Substances 0.000 description 1
- 235000004416 zinc carbonate Nutrition 0.000 description 1
- 229910000010 zinc carbonate Inorganic materials 0.000 description 1
- 239000004711 α-olefin Substances 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
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/10—Materials in mouldable or extrudable form for sealing or packing joints or covers
-
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/34—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
- C08G65/48—Polymers modified by chemical after-treatment
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L43/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing boron, silicon, phosphorus, selenium, tellurium or a metal; Compositions of derivatives of such polymers
- C08L43/04—Homopolymers or copolymers of monomers containing silicon
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
- C08L71/02—Polyalkylene oxides
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2200/00—Chemical nature of materials in mouldable or extrudable form for sealing or packing joints or covers
- C09K2200/06—Macromolecular organic compounds, e.g. prepolymers
- C09K2200/0615—Macromolecular organic compounds, e.g. prepolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C09K2200/0625—Polyacrylic esters or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2200/00—Chemical nature of materials in mouldable or extrudable form for sealing or packing joints or covers
- C09K2200/06—Macromolecular organic compounds, e.g. prepolymers
- C09K2200/0645—Macromolecular organic compounds, e.g. prepolymers obtained otherwise than by reactions involving carbon-to-carbon unsaturated bonds
- C09K2200/0657—Polyethers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Sealing Material Composition (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Description
(1)分子中に架橋性ケイ素基を有するポリオキシプロピレン系重合体(A)、側鎖に架橋性ケイ素基を有する(メタ)アクリル酸エステル系重合体(B)、および、末端のみに架橋性ケイ素基を有する(メタ)アクリル酸エステル系重合体(C)を含有する硬化性組成物。(ただし、(メタ)アクリル酸とはアクリル酸および/あるいはメタクリル酸のことを表す。)
(2)重合体(C)がリビングラジカル重合で製造されたものである(1)記載の硬化性組成物。
(3)重合体(C)が原子移動ラジカル重合で製造されたものである(2)記載の硬化性組成物。
(4)重合体(B)が、メチルエステル基を有する重合性単量体を含む(メタ)アクリル酸エステル単量体を重合させて得られたものである(1)記載の硬化性組成物。
(5)重合体(B)の分子量分布が1.8以上であり、重合体(C)の分子量分布が1.8以下である(1)から(4)のいずれかに記載の硬化性組成物。
(6)(A)、(B)、(C)の合計重量に占める(A)の重量が50%以下である(1)から(5)のいずれかに記載の硬化性組成物。
−R−O− (1)
(式中、Rは炭素数1〜4の2価のアルキレン基)で表わされるものが使用できるが、入手性が容易な点から、ポリオキシプロピレン系の重合体がより好ましい。このポリオキシプロピレン系重合体は、直鎖状であっても分枝状であってもよく、あるいは、これらの混合物であってもよい。また、他の単量体単位等が含まれていてもよいが、ポリオキシプロピレン系重合体を適度に低粘度化できる点や硬化物に適度な柔軟性を付与できる点から、オキシプロピレン単位が、ポリオキシプロピレン系重合体中に50重量%以上、好ましくは80重量%以上存在することが好ましい。
−[Si(R1 2-b)(Yb)O]mSi(R2 3-a)Ya (2)
(式中、R1及びR2は、いずれも炭素数1〜20のアルキル基、炭素数6〜20のアリール基、炭素数7〜20のアラルキル基または(R’)3SiO−で示されるトリオルガノシロキシ基を示し、R1またはR2が2個以上存在する時、それらは同一であってもよく、異なっていてもよい。ここでR’は炭素数1〜20の1価の炭化水素基であり、3個のR’は同一であってもよく、異なっていてもよい。Yは水酸基または加水分解性基を示し、Yが2個以上存在するときは、それらは同一であってもよく、異なっていてもよい。aは0、1、2、または3を、bは0、1、または2をそれぞれ示す。また、m個の一般式(3):
−Si(R1 2-b)(Yb)O− (3)
におけるbは異なっていてもよい。mは0〜19の整数を示す。但し、a+Σb≧1を満足するものとする。)
CH2=C(R3)COOR4 (4)
(式中、R3は水素原子またはメチル基、R4は炭素数1〜30のアルキル基を示す)
で表すことができる。本発明ではメチルエステル基を有する重合性単量体を使用することが好ましい。機構は明らかではないが成分(B)中のメチルエステル基の存在は本発明硬化性組成物を貯蔵した時の硬化速度の安定性に寄与するので好ましい。メチルエステル基を有する重合性単量体としてはアクリル酸メチル、メタアクリル酸メチルが例示されるがこれらに限定されない。
CH2=C(R3)COOR5−[Si(R1 2-b)(Yb)O]mSi(R2 3-a)Ya (5)
(式中、R3は前記に同じ。R5は炭素数1〜6の2価のアルキレン基を示す。R1,R2,Y,a,b,mは前記と同じ。)
または一般式(6):
CH2=C(R3)−[Si(R1 2-b)(Yb)O]mSi(R2 3-a)Ya (6)
(式中、R3,R1,R2,Y,a,b,mは前記と同じ。)で表される単量体、例えば、γ−メタクリロキシプロピルトリメトキシシラン、γ−メタクリロキシプロピルメチルジメトキシシラン、γ−メタクリロキシプロピルトリエトキシシラン等のγ−メタクリロキシプロピルポリアルコキシシラン、γ−アクリロキシプロピルトリメトキシシラン、γ−アクリロキシプロピルメチルジメトキシシラン、γ−アクリロキシプロピルトリエトキシシラン等のγ−アクリロキシプロピルポリアルコキシシラン、ビニルトリメトキシシラン、ビニルメチルジメトキシシラン、ビニルトリエトキシシラン等のビニルアルキルポリアルコキシシランなどがあげられる。
R9R10C(X)−R11−R12−C(R8)=CH2 (7)
(式中、R8は水素、またはメチル基、R9、R10は水素、または、炭素数1〜20の1価のアルキル基、アリール基、またはアラルキル、または他端において相互に連結したもの、R11は、−C(O)O−(エステル基)、−C(O)−(ケト基)、またはo−,m−,p−フェニレン基、R12は直接結合、または炭素数1〜20の2価の有機基で1個以上のエーテル結合を含んでいても良い、Xは前記に同じ)
XCH2C(O)O(CH2)kO(CH2)nCH=CH2、H3CC(H)(X)C(O)O(CH2)kO(CH2)nCH=CH2、(H3C)2C(X)C(O)O(CH2)kO(CH2)nCH=CH2、CH3CH2C(H)(X)C(O)O(CH2)kO(CH2)nCH=CH2、
o−,m−,p−XCH2−C6H4−(CH2)k−CH=CH2、o−,m−,p−CH3C(H)(X)−C6H4−(CH2)k−CH=CH2、o−,m−,p−CH3CH2C(H)(X)−C6H4−(CH2)k−CH=CH2(各式中、X、kは前記に同じ)、o−,m−,p−XCH2−C6H4−(CH2)k−O−(CH2)n−CH=CH2、o,m,p−CH3C(H)(X)−C6H4−(CH2)k−O−(CH2)n−CH=CH2、o−,m−,p−CH3CH2C(H)(X)−C6H4−(CH2)k−O−(CH2)nCH=CH2(各式中、X、n、kは前記に同じ)、
o−,m−,p−XCH2−C6H4−O−(CH2)n−CH=CH2、o−,m−,p−CH3C(H)(X)−C6H4−O−(CH2)n−CH=CH2、o−,m−,p−CH3CH2C(H)(X)−C6H4−O−(CH2)n−CH=CH2(各式中、X、nは前記に同じ)、o−,m−,p−XCH2−C6H4−O−(CH2)k−O−(CH2)n−CH=CH2、o−,m−,p−CH3C(H)(X)−C6H4−O−(CH2)k−O−(CH2)n−CH=CH2、o−,m−,p−CH3CH2C(H)(X)−C6H4−O−(CH2)k−O−(CH2)n−CH=CH2(各式中、X、n、kは前記に同じ)などがあげられる。
H2C=C(R8)−R12−C(R9)(X)−R13−R10 (8)
(式中、R8、R9、R10、R12、Xは上記に同じ、R13は、直接結合、−C(O)O−(エステル基)、−C(O)−(ケト基)、または、o−,m−,p−フェニレン基を表す)
R11は直接結合、または炭素数1〜20の2価の有機基(1個以上のエーテル結合を含んでいても良い)であるが、直接結合である場合は、ハロゲンの結合している炭素にビニル基が結合しており、ハロゲン化アリル化物である。この場合は、隣接ビニル基によって炭素−ハロゲン結合が活性化されているので、R13としてC(O)O基やフェニレン基等を有する必要は必ずしもなく、直接結合であってもよい。R12が直接結合でない場合は、炭素−ハロゲン結合を活性化するために、R13としてはC(O)O基、C(O)基、フェニレン基が好ましい。
R9R10C(X)−R11−R12−C(H)(R8)CH2−[Si(R15 2-b)(Yb)O]m−Si(R16 3-a)Ya (9)
(式中、R8、R9、R10、R11、R12、X、Y、a,b,mは前記に同じ、R15、R16は、いずれも炭素数1〜20のアルキル基、アリール基、アラルキル基、または(R’)3SiO−(R’は前記に同じ)で示されるトリオルガノシロキシ基を示し、R15またはR16が2個以上存在するとき、それらは同一であってもよく、異なっていてもよい。ただし、a+mb≧1であることを満足するものとする。)
(R16 3-a)(Ya)Si−[OSi(R15 2-b)(Yb)]m−CH2−C(H)(R8)−R12−C(R9)(X)−R13−R10 (10)
(式中、R8、R9、R10、R12、R13、R14、R15、a、b、m、X、Yは前記に同じ)
HO−(CH2)k−OC(O)C(H)(R17)(X)
(式中、X、kは前記に同じ、R17は水素原子または炭素数1〜20のアルキル基、アリール基、アラルキル基)
H2N−(CH2)k−OC(O)C(H)(R17)(X)
(上記の各式において、X、R17、kは前記に同じ)
−[Si(R18 2-b)(Yb)O]mSi(R19 3-a)Ya (11)
(式中、Y、a、b、mは前記に同じ、R18、R19はいずれも炭素数1〜20のアルキル基、炭素数6〜20のアリール基、炭素数7〜20のアラルキル基、または(R’)3SiO−(R’は前記に同じ)で示されるトリオルガノシロキシ基を示し、R18またはR19が2個以上存在するとき、それらは同一であってもよく、異なっていてもよい。ただし、a+mb≧1であることを満足するものとする。)
(2)水酸基を分子鎖末端に少なくとも1個有する重合体に、一分子中に架橋性ケイ素基とイソシアネート基のような水酸基と反応し得る基を併せ持つ化合物を反応させる方法、
(3)反応性の高い炭素−ハロゲン結合を分子鎖末端に少なくとも1個有する重合体に、一分子中に架橋性ケイ素基と安定なカルバニオンを有する化合物を反応させる方法、
などがあげられる。
H2C=C(R20)−R21−R22−C(R23)=CH2 (12)
(式中、R20は水素またはメチル基を示し、R21は−C(O)O−、またはo−,m−,p−フェニレン基を示し、R22は直接結合、または炭素数1〜20の2価の有機基を示し、1個以上のエーテル結合を含んでいてもよい。R23は水素、または炭素数1〜20のアルキル基、炭素数6〜20のアリール基または炭素数7〜20のアラルキル基を示す)
M+C-(R24)(R25)−R26−C(R23)=CH2 (13)
(式中、R23は前記に同じ、R24、R25はともにカルバニオンC-を安定化する電子吸引基であるか、または一方が前記電子吸引基で他方が水素または炭素数1〜10のアルキル基、またはフェニル基を示す。R26は直接結合、または炭素数1〜10の2価の有機基を示し、1個以上のエーテル結合を含んでいてもよい。M+はアルカリ金属イオン、または4級アンモニウムイオンを示す)
R24、R25の電子吸引基としては、−CO2R、−C(O)Rおよび−CNの構造を有するものが特に好ましい。
H2C=C(R23)−R27−O-M+ (14)
(式中、R23、M+は前記に同じ。R27は炭素数1〜20の2価の有機基で1個以上のエーテル結合を含んでいてもよい)
H2C=C(R23)−R28−C(O)O-M+ (15)
(式中、R23、M+は前記に同じ。R28は直接結合、または炭素数1〜20の2価の有機基で1個以上のエーテル結合を含んでいてもよい)などがあげられる。
(1−7)ナトリウムメトキシドのような塩基を作用させ、塩化アリルのようなアルケニル基含有ハロゲン化物と反応させる方法、
(1−8)アリルイソシアネート等のアルケニル基含有イソシアネート化合物を反応させる方法、
(1−9)(メタ)アクリル酸クロリドのようなアルケニル基含有酸ハロゲン化物をピリジン等の塩基存在下に反応させる方法、
(1−10)アクリル酸等のアルケニル基含有カルボン酸を酸触媒の存在下に反応させる方法、
などがあげられる。
H−[Si(R18 2-b)(Yb)O]m−Si(R19 3-a)Ya (16)
(式中、R18、R19、Y、a,b,mは前記に同じ。R18またはR19が2個以上存在するとき、それらは同一であってもよく、異なっていてもよい。ただし、a+mb≧1であることを満足するものとする。)
H−Si(R16 3-a)Ya (17)
(式中、R16、Y、aは前記に同じ)
で示される架橋性基を有する化合物が入手容易な点から好ましい。
H2C=C(R20)−R21−R22−OH (18)
(式中、R20、R21、R22は前記に同じ)
M+C-(R24)(R25)−R26−OH (19)
(式中、R24、R25、R26、は前記に同じ)
R24、R25の電子吸引基としては、−CO2R、−C(O)Rおよび−CNの構造を有するものが特に好ましい。
HO−R27−O-M+ (20)
(式中、R27およびM+は前記に同じ)
HO−R28−C(O)O-M+ (21)
(式中、R28およびM+は前記に同じ)
(式中、R20、R27は前記に同じ)
などの方法があげられる。
M+C-(R24)(R25)−R29−C(H)(R30)−CH2−[Si(R15 2-b)(Yb)O]m−Si(R16 3-a)Ya (23)
(式中、R15、R16、R24、R25、Y、a、b、m、は前記に同じ。R29は直接結合、または炭素数1〜10の2価の有機基で1個以上のエーテル結合を含んでいてもよい、R30は水素、または炭素数1〜10のアルキル基、炭素数6〜10のアリール基または炭素数7〜10のアラルキル基を示す。)
R24、R25の電子吸引基としては、−CO2R、−C(O)Rおよび−CNの構造を有するものが特に好ましい。
架橋性ケイ素基を有する重合体は、従来公知の各種縮合触媒の存在下、あるいは非存在下にシロキサン結合を形成することにより架橋、硬化する。硬化物の性状としては、重合体の分子量と主鎖骨格に応じて、ゴム状のものから樹脂状のものまで幅広く作製することができる。
本発明の組成物には、シランカップリング剤や、シランカップリング剤以外の接着性付与剤を添加することができる。接着付与剤を添加すると、外力により目地幅等が変動することによって、シーリング材がサイディングボード等の被着体から剥離する危険性をより低減することができる。また、場合によっては接着性向上の為に用いるプライマーの使用の必要性がなくなり、施工作業の簡略化が期待される。シランカップリング剤の具体例としてはアミノ基や、メルカプト基、エポキシ基、カルボキシル基、ビニル基、イソシアネート基、イソシアヌレート、ハロゲン等の官能基をもったシランカップリング剤が例示でき、その具体例としては、γ−イソシアネートプロピルトリメトキシシラン、γ−イソシアネートプロピルトリエトキシシラン、γ−イソシアネートプロピルメチルジエトキシシラン、γ−イソシアネートプロピルメチルジメトキシシラン等のイソシアネート基含有シラン類;γ−アミノプロピルトリメトキシシラン、γ−アミノプロピルトリエトキシシラン、γ−アミノプロピルトリイソプロポキシシラン、γ−アミノプロピルメチルジメトキシシラン、γ−アミノプロピルメチルジエトキシシラン、N−(2−アミノエチル)−3−アミノプロピルトリメトキシシラン、N−(2−アミノエチル)−3−アミノプロピルメチルジメトキシシラン、N−(2−アミノエチル)−3−アミノプロピルトリエトキシシラン、N−(2−アミノエチル)−3−アミノプロピルメチルジエトキシシラン、N−(2−アミノエチル)−3−アミノプロピルトリイソプロポキシシラン、γ−ウレイドプロピルトリメトキシシラン、N−フェニル−γ−アミノプロピルトリメトキシシラン、N−ベンジル−γ−アミノプロピルトリメトキシシラン、N−ビニルベンジル−γ−アミノプロピルトリエトキシシラン等のアミノ基含有シラン類;γ−メルカプトプロピルトリメトキシシラン、γ−メルカプトプロピルトリエトキシシラン、γ−メルカプトプロピルメチルジメトキシシラン、γ−メルカプトプロピルメチルジエトキシシラン等のメルカプト基含有シラン類;γ−グリシドキシプロピルトリメトキシシラン、γ−グリシドキシプロピルトリエトキシシラン、γ−グリシドキシプロピルメチルジメトキシシラン、β−(3,4−エポキシシクロヘキシル)エチルトリメトキシシラン、β−(3,4−エポキシシクロヘキシル)エチルトリエトキシシラン等のエポキシ基含有シラン類;β−カルボキシエチルトリエトキシシラン、β−カルボキシエチルフェニルビス(2−メトキシエトキシ)シラン、N−カルボキシメチル−β−アミノエチル−γ−アミノプロピルトリメトキシシラン等のカルボキシシラン類;ビニルトリメトキシシラン、ビニルトリエトキシシラン、γ−メタクリロイルオキシプロピルメチルジメトキシシラン、γ−アクロイルオキシプロピルトリエトキシシラン等のビニル型不飽和基含有シラン類;γ−クロロプロピルトリメトキシシラン等のハロゲン含有シラン類;トリス(トリメトキシシリル)イソシアヌレート等のイソシアヌレートシラン類等を挙げることができる。また、これらを変性した誘導体である、アミノ変性シリルポリマー、シリル化アミノポリマー、不飽和アミノシラン錯体、フェニルアミノ長鎖アルキルシラン、アミノシリル化シリコーン、ブロックイソシアネートシラン、シリル化ポリエステル等もシランカップリング剤として用いることができる。
本発明の硬化性組成物には、各種可塑剤を必要に応じて用いても良い。可塑剤を後述する充填材と併用して使用すると硬化物の伸びを大きくできたり、多量の充填材を混合できたりするためより有利となるが、必ずしも添加しなければならないものではない。可塑剤としては特に限定されないが、物性の調整、性状の調節等の目的により、例えば、ジブチルフタレート、ジヘプチルフタレート、ジ(2−エチルヘキシル)フタレート、ブチルベンジルフタレート等のフタル酸エステル類;ジオクチルアジペート、ジオクチルセバケート、ジブチルセバケート、コハク酸イソデシル等の非芳香族二塩基酸エステル類;オレイン酸ブチル、アセチルリシリノール酸メチル等の脂肪族エステル類;ジエチレングリコールジベンゾエート、トリエチレングリコールジベンゾエート、ペンタエリスリトールエステル等のポリアルキレングリコールのエステル類;トリクレジルホスフェート、トリブチルホスフェート等のリン酸エステル類;トリメリット酸エステル類;ポリスチレンやポリ−α−メチルスチレン等のポリスチレン類;ポリブタジエン、ポリブテン、ポリイソブチレン、ブタジエン−アクリロニトリル、ポリクロロプレン;塩素化パラフィン類;アルキルジフェニル、部分水添ターフェニル、等の炭化水素系油;プロセスオイル類;ポリエチレングリコール、ポリプロピレングリコール、ポリテトラメチレングリコール等のポリエーテルポリオールとこれらポリエーテルポリオールの水酸基をエステル基、エーテル基などに変換した誘導体等のポリエーテル類;エポキシ化大豆油、エポキシステアリン酸ベンジル等のエポキシ可塑剤類;セバシン酸、アジピン酸、アゼライン酸、フタル酸等の2塩基酸とエチレングリコール、ジエチレングリコール、トリエチレングリコール、プロピレングリコール、ジプロピレングリコール等の2価アルコールから得られるポリエステル系可塑剤類;アクリル系可塑剤を始めとするビニル系モノマーを種々の方法で重合して得られるビニル系重合体類等が挙げられる。
本発明の硬化性組成物には、各種充填材を必要に応じて用いても良い。充填材としては、特に限定されないが、木粉、パルプ、木綿チップ、アスベスト、ガラス繊維、炭素繊維、マイカ、クルミ殻粉、もみ殻粉、グラファイト、ケイソウ土、白土、シリカ(フュームドシリカ、沈降性シリカ、結晶性シリカ、溶融シリカ、ドロマイト、無水ケイ酸、含水ケイ酸等)、カーボンブラックのような補強性充填材;重質炭酸カルシウム、膠質炭酸カルシウム、炭酸マグネシウム、ケイソウ土、焼成クレー、クレー、タルク、酸化チタン、ベントナイト、有機ベントナイト、酸化第二鉄、べんがら、アルミニウム微粉末、フリント粉末、酸化亜鉛、活性亜鉛華、亜鉛末、炭酸亜鉛およびシラスバルーンなどのような充填材;石綿、ガラス繊維およびガラスフィラメント、炭素繊維、ケブラー繊維、ポリエチレンファイバー等のような繊維状充填材等が挙げられる。
また、更に、物性の大きな低下を起こすことなく軽量化、低コスト化を図ることを目的として、微小中空粒子をこれら補強性充填材に併用しても良い。
本発明の硬化性組成物には、必要に応じて生成する硬化物の引張特性を調整する物性調整剤を添加しても良い。
本発明の硬化性組成物には、硬化物の物性を変える等の必要に応じてシラノール含有化合物を添加しても良い。シラノール含有化合物とは、分子内に1個のシラノール基を有する化合物、及び/又は、水分と反応することにより分子内に1個のシラノール基を有する化合物を生成し得る化合物のことをいう。これらは一方のみを用いてもよいし、両化合物を同時に用いてもよい。
(CH3)3SiOH、(CH3CH2)3SiOH、(CH3CH2CH2)3SiOH、(n−Bu)3SiOH、(sec−Bu)3SiOH、(tert−Bu)3SiOH、(tert−Bu)Si(CH3)2OH、(C5H11)3SiOH、(C6H13)3SiOH、(C6H5)3SiOH、(C6H5)2Si(CH3)OH、(C6H5)Si(CH3)2OH、(C6H5)2Si(C2H5)OH、C6H5Si(C2H5)2OH、C6H5CH2Si(C2H5)2OH、C10H7Si(CH3)2OH
(ただし、上記式中C6H5はフェニル基を、C10H7はナフチル基を示す。)
等のような(R”)3SiOH(ただし式中R”は同一または異種の置換もしくは非置換のアルキル基またはアリール基)で表わすことができる化合物等のような主鎖が珪素、炭素、酸素からなるポリマー末端にシラノール基が結合した化合物等が例示できる。中でも、入手が容易であり、効果の点から分子量の小さい(CH3)3SiOH等が好ましい。
N,O−ビス(トリメチルシリル)アセトアミド、N−(トリメチルシリル)アセトアミド、ビス(トリメチルシリル)トリフルオロアセトアミド、N−メチル−N−トリメチルシリルトリフルオロアセトアミド、ビストリメチルシリル尿素、N−(tert−ブチルジメチルシリル)N−メチルトリフルオロアセトアミド、(N,N−ジメチルアミノ)トリメチルシラン、(N,N−ジエチルアミノ)トリメチルシラン、ヘキサメチルジシラザン、1,1,3,3−テトラメチルジシラザン、N−(トリメチルシリル)イミダゾール、トリメチルシリルトリフルオロメタンスルフォネート、トリメチルシリルフェノキシド、n−オクタノールのトリメチルシリル化物、2−エチルヘキサノールのトリメチルシリル化物、グリセリンのトリス(トリメチルシリル)化物、トリメチロールプロパンのトリス(トリメチルシリル)化物、ペンタエリスリトールのトリス(トリメチルシリル)化物、ペンタエリスリトールのテトラ(トリメチルシリル)化物、(CH3)3SiNHSi(CH3)3、(CH3)3SiNSi(CH3)2、アリロキシトリメチルシラン、N,O−ビス(トリメチルシリル)アセトアミド、N−(トリメチルシリル)アセトアミド、ビス(トリメチルシリル)トリフルオロアセトアミド、N−メチル−N−トリメチルシリルトリフルオロアセトアミド、ビストリメチルシリル尿素、N−(tert−ブチルジメチルシリル)N−メチルトリフルオロアセトアミド、(N,N−ジメチルアミノ)トリメチルシラン、(N,N−ジエチルアミノ)トリメチルシラン、ヘキサメチルジシラザン、1,1,3,3−テトラメチルジシラザン、N−(トリメチルシリル)イミダゾール、トリメチルシリルトリフルオロメタンスルフォネート、トリメチルシリルフェノキシド、n−オクタノールのトリメチルシリル化物、2−エチルヘキサノールのトリメチルシリル化物、グリセリンのトリス(トリメチルシリル)化物、トリメチロールプロパンのトリス(トリメチルシリル)化物、ペンタエリスリトールのトリス(トリメチルシリル)化物、ペンタエリスリトールのテトラ(トリメチルシリル)化物、
N,O−ビス(トリメチルシリル)アセトアミド、N−(トリメチルシリル)アセトアミド、トリメチルシリルフェノキシド、n−オクタノールのトリメチルシリル化物、2−エチルヘキサノールのトリメチルシリル化物、グリセリンのトリス(トリメチルシリル)化物、トリメチロールプロパンのトリス(トリメチルシリル)化物、ペンタエリスリトールのトリス(トリメチルシリル)化物、ペンタエリスリトールのテトラ(トリメチルシリル)等が挙げられるが、これらに限定されない。これらは単独で用いてもよく、2種以上を併用してもよい。
本発明の硬化性組成物には、必要に応じて垂れを防止し、作業性を良くするためにチクソ性付与剤(垂れ防止剤)を添加しても良い。
本発明の硬化性組成物には、必要に応じて光硬化性物質を添加しても良い。光硬化性物質とは、光の作用によって短時間に、分子構造が化学変化をおこし、硬化などの物性的変化を生ずるものである。この光硬化性物質を添加することにより、硬化性組成物を硬化させた際の硬化物表面の粘着性(残留タックともいう)を低減できる。この光硬化性物質は、光をあてることにより硬化し得る物質であるが、代表的な光硬化性物質は、例えば室内の日の当たる位置(窓付近)に1日間、室温で静置することにより硬化させることができる物質である。この種の化合物には、有機単量体、オリゴマー、樹脂あるいはそれらを含む組成物など多くのものが知られており、その種類は特に限定されないが、例えば、不飽和アクリル系化合物、ポリケイ皮酸ビニル類あるいはアジド化樹脂等が挙げられる。
本発明の硬化性組成物には、必要に応じて空気酸化硬化性物質を添加しても良い。空気酸化硬化性物質とは、空気中の酸素により架橋硬化できる不飽和基を有する化合物である。この空気酸化硬化性物質を添加することにより、硬化性組成物を硬化させた際の硬化物表面の粘着性(残留タックともいう)を低減できる。本発明における空気酸化硬化性物質は、空気と接触させることにより硬化し得る物質であり、より具体的には、空気中の酸素と反応して硬化する性質を有するものである。代表的な空気酸化硬化性物質は、例えば空気中で室内に1日間静置することにより硬化させることができる。
本発明の硬化性組成物には、必要に応じて酸化防止剤を添加しても良い。酸化防止剤は各種のものが知られており、例えば大成社発行の「酸化防止剤ハンドブック」、シーエムシー化学発行の「高分子材料の劣化と安定化」(235〜242)等に記載された種々のものが挙げられるが、これらに限定されるわけではない。
2,6−ジ−tert−ブチル−4−メチルフェノール、2,6−ジ−tert−ブチル−4−エチルフェノール、モノ(又はジ又はトリ)(αメチルベンジル)フェノール、2,2’−メチレンビス(4エチル−6−tert−ブチルフェノール)、2,2’−メチレンビス(4メチル−6−tert−ブチルフェノール)、4,4’−ブチリデンビス(3−メチル−6−tert−ブチルフェノール)、4,4’−チオビス(3−メチル−6−tert−ブチルフェノール)、2,5−ジ−tert−ブチルハイドロキノン、2,5−ジ−tert−アミルハイドロキノン、トリエチレングリコール−ビス−[3−(3−tert−ブチル−5−メチル−4ヒドロキシフェニル)プロピオネート]、1,6−ヘキサンジオール−ビス[3−(3,5−ジ−tert−ブチル−4−ヒドロキシフェニル)プロピオネート]、2,4−ビス−(n−オクチルチオ)−6−(4−ヒドロキシ−3,5−ジ−tert−ブチルアニリノ)−1,3,5−トリアジン、ペンタエリスリチル−テトラキス[3−(3,5−ジ−tert−ブチル−4−ヒドロキシフェニル)プロピオネート]、2,2−チオ−ジエチレンビス[3−(3,5−ジ−tert−ブチル−4−ヒドロキシフェニル)プロピオネート]、オクタデシル−3−(3,5−ジ−tert−ブチル−4−ヒドロキシフェニル)プロピオネート、N,N’−ヘキサメチレンビス(3,5−ジ−tert−ブチル−4−ヒドロキシ−ヒドロシンナマミド)、3,5−ジ−tert−ブチル−4−ヒドロキシ−ベンジルフォスフォネート−ジエチルエステル、1,3,5−トリメチル−2,4,6−トリス(3,5−ジ−tert−ブチル−4−ヒドロキシベンジル)ベンゼン、ビス(3,5−ジ−tert−ブチル−4−ヒドロキシベンジルホスホン酸エチル)カルシウム、トリス−(3,5−ジ−tert−ブチル−4−ヒドロキシベンジル)イソシアヌレート、2,4−2,4−ビス[(オクチルチオ)メチル]o−クレゾール、N,N’−ビス[3−(3,5−ジ−tert−ブチル−4−ヒドロキシフェニル)プロピオニル]ヒドラジン、トリス(2,4−ジ−tert−ブチルフェニル)フォスファイト、2−(5−メチル−2−ヒドロキシフェニル)ベンゾトリアゾール、2−[2−ヒドロキシ−3,5−ビス(α,α−ジメチルベンジル)フェニル]−2H−ベンゾトリアゾール、2−(3,5−ジ−tert−ブチル−2−ヒドロキシフェニル)ベンゾトリアゾール、2−(3−tert−ブチル−5−メチル−2−ヒドロキシフェニル)−5−クロロベンゾトリアゾール、2−(3,5−ジ−tert−ブチル−2−ヒドロキシフェニル)−5−クロロベンゾトリアゾール、2−(3,5−ジ−tert−アミル−2−ヒドロキシフェニル)ベンゾトリアゾール、2−(2’−ヒドロキシ−5’−tert−オクチルフェニル)−ベンゾトリアゾール、メチル−3−[3−tert−ブチル−5−(2H−ベンゾトリアゾール−2−イル)−4−ヒドロキシフェニル]プロピオネート−ポリエチレングリコール(分子量約300)との縮合物、ヒドロキシフェニルベンゾトリアゾール誘導体、2−(3,5−ジ−tert−ブチル−4−ヒドロキシベンジル)−2−n−ブチルマロン酸ビス(1,2,2,6,6−ペンタメチル−4−ピペリジル)、2,4−ジ−tert−ブチルフェニル−3,5−ジ−tert−ブチル−4−ヒドロキシベンゾエート等が挙げられる。
本発明の硬化性組成物には、必要に応じて光安定剤を添加しても良い。光安定剤は各種のものが知られており、例えば大成社発行の「酸化防止剤ハンドブック」、シーエムシー化学発行の「高分子材料の劣化と安定化」(235〜242)等に記載された種々のものが挙げられるが、これらに限定されるわけではない。
コハク酸ジメチル−1−(2−ヒドロキシエチル)−4−ヒドロキシ−2,2,6,6−テトラメチルピペリジン重縮合物、ポリ[{6−(1,1,3,3−テトラメチルブチル)アミノ−1,3,5−トリアジン−2,4−ジイル}{(2,2,6,6−テトラメチル−4−ピペリジル)イミノ}]、N,N’−ビス(3アミノプロピル)エチレンジアミン−2,4−ビス[N−ブチル−N−(1,2,2,6,6−ペンタメチル−4−ピペリジル)アミノ]−6−クロロ−1,3,5−トリアジン縮合物、ビス(2,2,6,6−テトラメチル−4−ピペリジル)セバケート、コハク酸−ビス(2,2,6,6−テトラメチル−4−ピペリディニル)エステル等が挙げられる。
本発明の硬化性組成物には、硬化性組成物又は硬化物の諸物性の調整を目的として、必要に応じて各種添加剤を添加してもよい。このような添加物の例としては、たとえば、難燃剤、硬化性調整剤、老化防止剤、ラジカル禁止剤、紫外線吸収剤、金属不活性化剤、オゾン劣化防止剤、リン系過酸化物分解剤、滑剤、顔料、発泡剤、光硬化性樹脂などがあげられる。これらの各種添加剤は単独で用いてもよく、2種類以上を併用してもよい。
GPC測定(ポリスチレン換算)による数平均分子量が約3,000のポリオキシプロピレングリコール420gと数平均分子量が約3,000のポリオキシプロピレントリオール80gの混合物に水酸化ナトリウム40gを加え、60℃で13時間反応させた後、ブロモクロルメタン19gを添加し、60℃で10時間反応させた。得られた重合体の分子量分布は2.1であり、粘度は385ポイズであった。続いて、この重合体に塩化アリル15gを加え36時間反応させた後、ケイ酸アルミニウムで吸着処理した。この処理後の重合体500gに、塩化白金酸の触媒を添加した後、ジメトキシメチルシラン12gを加えて80℃で4時間反応させた。その結果、重合体末端に架橋性シリル基を少なくとも1個有するポリオキシプロピレン系重合体(重合体a)を得た。
窒素雰囲気下、温度を100〜110℃に保ったトルエン240g中に、メタクリル酸メチル74g、アクリル酸ブチル351g、アクリル酸2−エチルヘキシル52.5g、γ−メタクリロキシプロピルメチルジメトキシシラン22.5g、2,2’−アゾビス(2−メチルブチロニトリル)10.85gおよびトルエン100gの混合溶液を調製し、滴下して重合を行った。その結果、GPC測定(ポリスチレン換算)による数平均分子量が約7,800の分子中に架橋性シリル基を少なくとも1個有する(メタ)アクリル酸アルキルエステル系重合体(重合体b)のトルエン溶液を得た。
50mlフラスコに臭化第一銅0.63g、ペンタメチルジエチレントリアミン0.76g、アセトニトリル5ml、2,5−ジブロモアジピン酸ジエチル1.6g、アクリル酸ブチル44.7gを仕込み、凍結脱気をおこなった後、窒素雰囲気下で70℃で7時間反応させた。活性アルミナのカラムを通して銅触媒を除去精製することにより末端に臭素基を有する重合体を得た。この末端に臭素基を有する重合体35g、ペンテン酸カリウム2.2g、N,N−ジメチルアセトアミド35mlを200mlフラスコに仕込み、70℃で4時間反応させた。反応混合液中の未反応のペンテン酸カリウムおよび生成した臭化カリウムを水抽出精製により除去し、末端にアルケニル基を有する重合体を得た。この末端にアルケニル基を有する重合体15g、ジメトキシメチルシラン1.8ml、オルト蟻酸メチル0.26ml、白金ビス(ジビニルテトラメチルジシロキサン)10-4mmolを200ml耐圧反応管に仕込み、100℃で4時間反応させ、GPC測定(ポリスチレン換算)による数平均分子量が約11,900の重合体末端に架橋性シリル基を少なくとも1個有するアクリル酸ブチル系重合体(重合体c)を得た。
合成例1で得た重合体aと合成例2で得た重合体bのトルエン溶液とを固形分比で49重量部:21重量部となるように混合した後、加熱減圧下でトルエンを除去し重合体混合物1を得た。
合成例1で得た重合体aと合成例2で得た重合体bのトルエン溶液とを固形分比で49重量部:51重量部となるように混合した後、加熱減圧下でトルエンを除去し重合体混合物2を得た。
5リットルのプラネタリーミキサーに表面処理炭酸カルシウム(白艶華CCR:白石工業)120重量部と酸化チタン(タイペーク R−820:石原産業)20重量部を入れて、減圧下120℃で2時間乾燥を行なった。これに重合体成分として合成例4で得た重合体混合物1の70重量部と合成例3で得た重合体cの30重量部、可塑剤としてフタル酸エステル化合物(ジイソデシルフタレート:ジェイ・プラス)55重量部、タレ防止剤(ディスパロン #6500:楠本化成)2重量部、紫外線吸収剤(チヌビン327:チバ・スペシャルティ・ケミカルズ)1重量部、光安定剤(サノール LS770:三共)1重量部を投入し、さらに減圧下120℃で2時間攪拌を行なった。室温まで冷却後、脱水剤(A−171:日本ユニカー)2重量部、接着付与剤(A−1120:日本ユニカー)3重量部、硬化触媒(ネオスタン U−220:日東化成)2重量部を投入して、さらに30分間室温で攪拌した後、カートリッジに充填することにより硬化性組成物1を作製した。
重合体成分として合成例5で得た重合体混合物2を100重量部用いたほかは実施例1と同様に操作を行ない、硬化性組成物2を作製した。
重合体成分として合成例1で得た重合体aを49重量部と合成例3で得た重合体cを51重量部用いたほかは実施例1と同様に操作を行ない、硬化性組成物3を作製した。
主鎖骨格が複合金属シアン化物錯体触媒を用いて得られたものであり、分子末端にアリルエーテル基を導入した平均分子量約19,000のポリオキシプロピレン500gを攪拌機付耐圧反応容器に入れ、メチルジメトキシシラン4.6gと塩化白金酸触媒(塩化白金酸六水和物)1×10-4[eq/ビニル基]を加え、90℃で2時間反応させた後、未反応のメチルジメトキシシランを減圧留去して末端に架橋性シリル基を少なくとも1個有するポリオキシプロピレン系重合体(重合体d)を得た。
窒素雰囲気下、温度を100〜110℃に保ったトルエン250g中に、アクリル酸ブチル340g、メタクリル酸メチル50g、メタクリル酸ステアリル100g、γ−メタクリロキシプロピルメチルジメトキシシラン10g、和光純薬製V−59 2.5g、トルエン100gを溶かした溶液を4時間かけて滴下して重合を行った。その結果、GPC測定(ポリスチレン換算)による数平均分子量が約18,000の分子中に架橋性シリル基を少なくとも1個有する(メタ)アクリル酸アルキルエステル系重合体(重合体e)のトルエン溶液を得た。
2Lフラスコに臭化第一銅8.39g、ペンタメチルジエチレントリアミン(以後トリアミンと称す)0.41mL、アセトニトリル112mL、2,5−ジブロモアジピン酸ジエチル17.6g、アクリル酸ブチル224mLを加え、70℃で加熱しトリアミン1.84mLを追加しながら断続的にアクリル酸ブチル895mLを滴下、さらに1,7−オクタジエン288mL、トリアミン4.1mLを添加し70℃で8時間反応させた。得られた重合体のGPC測定(ポリスチレン換算)による数平均分子量は24,100、分子量分布は1.27であり、また1H−NMR分析より求めた重合体1分子あたりのアルケニル基の個数は2.6個であった。1L耐圧反応容器に、精製後の重合体648g、ジメトキシメチルヒドロシラン25.5mL、オルトぎ酸メチル7.54mLおよび白金ビス(ジビニルテトラメチルジシロキサン)を重合体のアルケニル基に対してモル比で3×10-3当量仕込み100℃で2時間反応させ、GPC測定(ポリスチレン換算)による数平均分子量が29,600、1H−NMR分析により求めた1分子当たりに導入された平均のシリル基の数が1.9個のアクリル酸ブチル系重合体(重合体f)を得た。
5リットルのプラネタリーミキサーに表面処理炭酸カルシウム(白艶華CCR:白石工業)150重量部と重質炭酸カルシウム(ナノックス25A:丸尾カルシウム)20重量部および酸化チタン(タイペーク R−820:石原産業)10重量部を入れて、減圧下120℃で2時間乾燥を行なった。これに重合体成分として合成例8で得た重合体fを70重量部、合成例6で得た重合体dを21重量部、合成例7で得た重合体eを9重量部、可塑剤としてフタル酸エステル化合物(ジイソデシルフタレート:ジェイ・プラス)60重量部、タレ防止剤(ディスパロン #6500:楠本化成)2重量部、紫外線吸収剤(チヌビン213:チバ・スペシャルティ・ケミカルズ)1重量部、光安定剤(サノール LS770:三共)1重量部を投入し、さらに減圧下120℃で2時間攪拌を行なった。室温まで冷却後、脱水剤(A−171:日本ユニカー)2重量部、接着付与剤(A−1120:日本ユニカー)2重量部、硬化触媒(ネオスタン U−220:日東化成)2重量部を投入して、さらに30分間室温で攪拌した後、カートリッジに充填することにより硬化性組成物4を作製した。
重合体成分として合成例7で得た重合体e(9重量部)の代わりに、合成例6で得た重合体d(9重量部)を用いた(すなわち重合体dを合計30重量部用いた)こと以外は実施例2と同様に操作を行ない硬化性組成物5を作製した。
重合体成分として合成例8の重合体fを全量(すなわち100重量部)用いたほかは実施例2と同様に操作を行ない硬化性組成物6を作製した。
硬化性組成物のカートリッジを50℃の乾燥機中で2週間および4週間貯蔵した。貯蔵前後の硬化性組成物の皮張り時間を測定して、遅延率を求めることにより、貯蔵安定性の評価を行なった。
硬化性組成物を金属製容器(内径45mm×深さ9mm)に気泡を巻き込まないように充填した後、表面をヘラでかきとり平らにした。この時の時間を測定開始時間とした。スパチュラを用いて表面を軽く押さえて硬化性組成物がスパチュラに付着するかどうかを目視で観察した。硬化性組成物がスパチュラに付着しなくなった時を測定の終了時間とした。測定開始から終了までに要した時間を皮張り時間とした。測定は23±2℃、湿度50±5%で行なった。
遅延率=(50℃貯蔵後の皮張り時間)÷(初期の皮張り時間)
硬化性組成物を厚さ3mmの型枠に充填して、23℃で3日間静置後、続いて50℃で4日間加熱することによりゴム状シートを得た。ゴム状シートからJIS K 6251記載の3号形ダンベルを打ち抜いて引張物性を測定し、100%モジュラスと破断時の強度および伸びを測定した。表2から実施例2の硬化性組成物は比較例3および比較例4の硬化性組成物よりも遅延率が小さく、貯蔵安定性に優れていた。また表1から実施例1の硬化物の引張物性における100%モジュラスと破断時の伸びは、比較例1の値と比較例2の値とを用いた比例計算によって推定される値より、100%モジュラスはより低く、破断時伸びはより大きな値が得られた。
Claims (5)
- 分子中に架橋性ケイ素基を有するポリオキシプロピレン系重合体(A)、側鎖に架橋性ケイ素基を有する(メタ)アクリル酸エステル系重合体(B)、および、末端のみに架橋性ケイ素基を有する(メタ)アクリル酸エステル系重合体(C)を含有し、
重合体(B)がメチルエステル基を有する重合性単量体を含む(メタ)アクリル酸エステル単量体を重合させて得られたものである硬化性組成物。 - 重合体(C)がリビングラジカル重合で製造されたものである請求項1記載の硬化性組成物。
- 重合体(C)が原子移動ラジカル重合で製造されたものである請求項2記載の硬化性組成物。
- 重合体(B)の分子量分布が1.8以上であり、重合体(C)の分子量分布が1.8以下である請求項1から3のいずれか一項に記載の硬化性組成物。
- (A)、(B)、(C)の合計重量に占める(A)の重量が50%以下である請求項1から4のいずれか一項に記載の硬化性組成物。
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JP2006225487A (ja) * | 2005-02-16 | 2006-08-31 | Kaneka Corp | 硬化性組成物 |
JP2006225530A (ja) * | 2005-02-18 | 2006-08-31 | Kaneka Corp | 硬化性組成物 |
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JP5069852B2 (ja) * | 2005-09-30 | 2012-11-07 | アイカ工業株式会社 | 接着剤 |
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JP5188698B2 (ja) * | 2006-11-06 | 2013-04-24 | モメンティブ・パフォーマンス・マテリアルズ・ジャパン合同会社 | 硬化性組成物 |
DE102007038030B4 (de) * | 2007-08-10 | 2009-07-09 | Henkel Ag & Co. Kgaa | Härtbare Zusammensetzungen aus Dimethoxysilanen |
EP2246373B1 (en) * | 2008-02-05 | 2017-07-19 | Denka Company Limited | Acrylic rubber |
WO2009126186A1 (en) | 2008-04-10 | 2009-10-15 | Cardinal Ig Company | Manufacturing of photovoltaic subassemblies |
WO2009145245A1 (ja) * | 2008-05-30 | 2009-12-03 | 東亞合成株式会社 | 硬化性組成物 |
US9482946B2 (en) * | 2011-03-30 | 2016-11-01 | Hitachi Chemical Company, Ltd. | Photosensitive resin composition, photosensitive element using same, method for forming partition wall of image display device, and method for manufacturing image display device |
KR101369381B1 (ko) * | 2011-11-04 | 2014-03-06 | 에스케이이노베이션 주식회사 | 함불소 화합물을 포함하는 저굴절 코팅 조성물, 이를 이용한 반사방지 필름, 이를 포함하는 편광판 및 표시장치 |
EP3347395B1 (en) * | 2015-09-10 | 2020-04-22 | Dow Global Technologies LLC | Moisture curable systems based on polysilylated polyethers and titanium (iv) catalsts and/or zinc/cyclic amidine catalyst mixtures |
GB201604971D0 (en) * | 2016-03-23 | 2016-05-04 | Dow Corning | Moisture curable compositions |
WO2019058795A1 (ja) * | 2017-09-20 | 2019-03-28 | 東亞合成株式会社 | 硬化性組成物、シーリング材組成物、及び接着剤組成物 |
JP7461338B2 (ja) * | 2019-03-28 | 2024-04-03 | 株式会社カネカ | 硬化性組成物、及び硬化物 |
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