JP6032383B1 - 活性エネルギー線硬化性樹脂組成物、塗料、塗膜、及びフィルム - Google Patents
活性エネルギー線硬化性樹脂組成物、塗料、塗膜、及びフィルム Download PDFInfo
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- JP6032383B1 JP6032383B1 JP2016514186A JP2016514186A JP6032383B1 JP 6032383 B1 JP6032383 B1 JP 6032383B1 JP 2016514186 A JP2016514186 A JP 2016514186A JP 2016514186 A JP2016514186 A JP 2016514186A JP 6032383 B1 JP6032383 B1 JP 6032383B1
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- 238000000576 coating method Methods 0.000 title claims abstract description 106
- 239000011248 coating agent Substances 0.000 title claims abstract description 103
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- 150000001875 compounds Chemical class 0.000 claims abstract description 124
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 claims abstract description 110
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 102
- 238000000034 method Methods 0.000 claims abstract description 84
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- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 165
- 229920000058 polyacrylate Polymers 0.000 claims description 130
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- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 17
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- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 14
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- 125000004432 carbon atom Chemical group C* 0.000 description 10
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- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 9
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- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 description 8
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- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 5
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- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 4
- WMYINDVYGQKYMI-UHFFFAOYSA-N 2-[2,2-bis(hydroxymethyl)butoxymethyl]-2-ethylpropane-1,3-diol Chemical compound CCC(CO)(CO)COCC(CC)(CO)CO WMYINDVYGQKYMI-UHFFFAOYSA-N 0.000 description 4
- FDSUVTROAWLVJA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol;prop-2-enoic acid Chemical compound OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OCC(CO)(CO)COCC(CO)(CO)CO FDSUVTROAWLVJA-UHFFFAOYSA-N 0.000 description 4
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 4
- GWZMWHWAWHPNHN-UHFFFAOYSA-N 2-hydroxypropyl prop-2-enoate Chemical compound CC(O)COC(=O)C=C GWZMWHWAWHPNHN-UHFFFAOYSA-N 0.000 description 4
- JYSWMLAADBQAQX-UHFFFAOYSA-N 2-prop-2-enoyloxyacetic acid Chemical compound OC(=O)COC(=O)C=C JYSWMLAADBQAQX-UHFFFAOYSA-N 0.000 description 4
- VVBLNCFGVYUYGU-UHFFFAOYSA-N 4,4'-Bis(dimethylamino)benzophenone Chemical compound C1=CC(N(C)C)=CC=C1C(=O)C1=CC=C(N(C)C)C=C1 VVBLNCFGVYUYGU-UHFFFAOYSA-N 0.000 description 4
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- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- TUOBEAZXHLTYLF-UHFFFAOYSA-N [2-(hydroxymethyl)-2-(prop-2-enoyloxymethyl)butyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(CC)COC(=O)C=C TUOBEAZXHLTYLF-UHFFFAOYSA-N 0.000 description 4
- 125000005396 acrylic acid ester group Chemical group 0.000 description 4
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
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- 238000002360 preparation method Methods 0.000 description 4
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- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
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- FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 description 3
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- GJKGAPPUXSSCFI-UHFFFAOYSA-N 2-Hydroxy-4'-(2-hydroxyethoxy)-2-methylpropiophenone Chemical compound CC(C)(O)C(=O)C1=CC=C(OCCO)C=C1 GJKGAPPUXSSCFI-UHFFFAOYSA-N 0.000 description 3
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- HEMYIEDNNZJZSV-UHFFFAOYSA-N 4-prop-2-enoyloxybutanoic acid Chemical compound OC(=O)CCCOC(=O)C=C HEMYIEDNNZJZSV-UHFFFAOYSA-N 0.000 description 3
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- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 3
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- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 3
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- QASBHTCRFDZQAM-UHFFFAOYSA-N (2-isocyanato-2-methyl-3-prop-2-enoyloxypropyl) prop-2-enoate Chemical compound C=CC(=O)OCC(C)(COC(=O)C=C)N=C=O QASBHTCRFDZQAM-UHFFFAOYSA-N 0.000 description 2
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- XSCLFFBWRKTMTE-UHFFFAOYSA-N 1,3-bis(isocyanatomethyl)cyclohexane Chemical compound O=C=NCC1CCCC(CN=C=O)C1 XSCLFFBWRKTMTE-UHFFFAOYSA-N 0.000 description 2
- VGHSXKTVMPXHNG-UHFFFAOYSA-N 1,3-diisocyanatobenzene Chemical compound O=C=NC1=CC=CC(N=C=O)=C1 VGHSXKTVMPXHNG-UHFFFAOYSA-N 0.000 description 2
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- CDMDQYCEEKCBGR-UHFFFAOYSA-N 1,4-diisocyanatocyclohexane Chemical compound O=C=NC1CCC(N=C=O)CC1 CDMDQYCEEKCBGR-UHFFFAOYSA-N 0.000 description 2
- SBJCUZQNHOLYMD-UHFFFAOYSA-N 1,5-Naphthalene diisocyanate Chemical compound C1=CC=C2C(N=C=O)=CC=CC2=C1N=C=O SBJCUZQNHOLYMD-UHFFFAOYSA-N 0.000 description 2
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- UZKWTJUDCOPSNM-UHFFFAOYSA-N 1-ethenoxybutane Chemical compound CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 2
- 239000012956 1-hydroxycyclohexylphenyl-ketone Substances 0.000 description 2
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- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- ZWWQRMFIZFPUAA-UHFFFAOYSA-N dimethyl 2-methylidenebutanedioate Chemical compound COC(=O)CC(=C)C(=O)OC ZWWQRMFIZFPUAA-UHFFFAOYSA-N 0.000 description 1
- LDCRTTXIJACKKU-ONEGZZNKSA-N dimethyl fumarate Chemical compound COC(=O)\C=C\C(=O)OC LDCRTTXIJACKKU-ONEGZZNKSA-N 0.000 description 1
- 229960004419 dimethyl fumarate Drugs 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- CJSBUWDGPXGFGA-UHFFFAOYSA-N dimethyl-butadiene Natural products CC(C)=CC=C CJSBUWDGPXGFGA-UHFFFAOYSA-N 0.000 description 1
- PODOEQVNFJSWIK-UHFFFAOYSA-N diphenylphosphoryl-(2,4,6-trimethoxyphenyl)methanone Chemical compound COC1=CC(OC)=CC(OC)=C1C(=O)P(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 PODOEQVNFJSWIK-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- KGGOIDKBHYYNIC-UHFFFAOYSA-N ditert-butyl 4-[3,4-bis(tert-butylperoxycarbonyl)benzoyl]benzene-1,2-dicarboperoxoate Chemical compound C1=C(C(=O)OOC(C)(C)C)C(C(=O)OOC(C)(C)C)=CC=C1C(=O)C1=CC=C(C(=O)OOC(C)(C)C)C(C(=O)OOC(C)(C)C)=C1 KGGOIDKBHYYNIC-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 description 1
- 235000019414 erythritol Nutrition 0.000 description 1
- 229940009714 erythritol Drugs 0.000 description 1
- 239000003759 ester based solvent Substances 0.000 description 1
- MEGHWIAOTJPCHQ-UHFFFAOYSA-N ethenyl butanoate Chemical compound CCCC(=O)OC=C MEGHWIAOTJPCHQ-UHFFFAOYSA-N 0.000 description 1
- UYYOUWIRVXKLMP-UHFFFAOYSA-N ethyl 2-[n-(2-ethoxy-2-oxoethyl)-2-(1,3,5-triazin-2-yl)-3,5-bis(trichloromethyl)anilino]acetate Chemical compound CCOC(=O)CN(CC(=O)OCC)C1=CC(C(Cl)(Cl)Cl)=CC(C(Cl)(Cl)Cl)=C1C1=NC=NC=N1 UYYOUWIRVXKLMP-UHFFFAOYSA-N 0.000 description 1
- BHXIWUJLHYHGSJ-UHFFFAOYSA-N ethyl 3-ethoxypropanoate Chemical compound CCOCCC(=O)OCC BHXIWUJLHYHGSJ-UHFFFAOYSA-N 0.000 description 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000007667 floating Methods 0.000 description 1
- XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical compound FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 125000003827 glycol group Chemical group 0.000 description 1
- 238000007646 gravure printing Methods 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229940035429 isobutyl alcohol Drugs 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- JMMWKPVZQRWMSS-UHFFFAOYSA-N isopropanol acetate Natural products CC(C)OC(C)=O JMMWKPVZQRWMSS-UHFFFAOYSA-N 0.000 description 1
- 229940011051 isopropyl acetate Drugs 0.000 description 1
- QPPQHRDVPBTVEV-UHFFFAOYSA-N isopropyl dihydrogen phosphate Chemical compound CC(C)OP(O)(O)=O QPPQHRDVPBTVEV-UHFFFAOYSA-N 0.000 description 1
- GWYFCOCPABKNJV-UHFFFAOYSA-M isovalerate Chemical compound CC(C)CC([O-])=O GWYFCOCPABKNJV-UHFFFAOYSA-M 0.000 description 1
- 229910003002 lithium salt Inorganic materials 0.000 description 1
- 159000000002 lithium salts Chemical class 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- RBQRWNWVPQDTJJ-UHFFFAOYSA-N methacryloyloxyethyl isocyanate Chemical compound CC(=C)C(=O)OCCN=C=O RBQRWNWVPQDTJJ-UHFFFAOYSA-N 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- 125000001421 myristyl 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])[H] 0.000 description 1
- KTQDYGVEEFGIIL-UHFFFAOYSA-N n-fluorosulfonylsulfamoyl fluoride Chemical class FS(=O)(=O)NS(F)(=O)=O KTQDYGVEEFGIIL-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- XGFDHKJUZCCPKQ-UHFFFAOYSA-N nonadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCO XGFDHKJUZCCPKQ-UHFFFAOYSA-N 0.000 description 1
- 125000001400 nonyl 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])[H] 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 1
- 125000002347 octyl 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])[H] 0.000 description 1
- 238000007645 offset printing Methods 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000012788 optical film Substances 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 125000001741 organic sulfur group Chemical group 0.000 description 1
- JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 description 1
- LXTZRIBXKVRLOA-UHFFFAOYSA-N padimate a Chemical class CCCCCOC(=O)C1=CC=C(N(C)C)C=C1 LXTZRIBXKVRLOA-UHFFFAOYSA-N 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 description 1
- 239000006223 plastic coating Substances 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920013716 polyethylene resin Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 description 1
- 239000003223 protective agent Substances 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical compound C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- MUTNCGKQJGXKEM-UHFFFAOYSA-N tamibarotene Chemical compound C=1C=C2C(C)(C)CCC(C)(C)C2=CC=1NC(=O)C1=CC=C(C(O)=O)C=C1 MUTNCGKQJGXKEM-UHFFFAOYSA-N 0.000 description 1
- OPQYOFWUFGEMRZ-UHFFFAOYSA-N tert-butyl 2,2-dimethylpropaneperoxoate Chemical compound CC(C)(C)OOC(=O)C(C)(C)C OPQYOFWUFGEMRZ-UHFFFAOYSA-N 0.000 description 1
- GSECCTDWEGTEBD-UHFFFAOYSA-N tert-butylperoxycyclohexane Chemical compound CC(C)(C)OOC1CCCCC1 GSECCTDWEGTEBD-UHFFFAOYSA-N 0.000 description 1
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 125000002889 tridecyl 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])[H] 0.000 description 1
- JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 description 1
- YFNKIDBQEZZDLK-UHFFFAOYSA-N triglyme Chemical compound COCCOCCOCCOC YFNKIDBQEZZDLK-UHFFFAOYSA-N 0.000 description 1
- QEDNBHNWMHJNAB-UHFFFAOYSA-N tris(8-methylnonyl) phosphite Chemical compound CC(C)CCCCCCCOP(OCCCCCCCC(C)C)OCCCCCCCC(C)C QEDNBHNWMHJNAB-UHFFFAOYSA-N 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 150000007964 xanthones Chemical class 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
- B32B27/20—Layered products comprising a layer of synthetic resin characterised by the use of special additives using fillers, pigments, thixotroping agents
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/30—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/30—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
- B32B27/308—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers comprising acrylic (co)polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/44—Polymerisation in the presence of compounding ingredients, e.g. plasticisers, dyestuffs, fillers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F292/00—Macromolecular compounds obtained by polymerising monomers on to inorganic materials
-
- 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
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
-
- 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
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
-
- 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
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/61—Additives non-macromolecular inorganic
- C09D7/62—Additives non-macromolecular inorganic modified by treatment with other compounds
-
- 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
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/66—Additives characterised by particle size
- C09D7/67—Particle size smaller than 100 nm
-
- 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
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/66—Additives characterised by particle size
- C09D7/68—Particle size between 100-1000 nm
-
- 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
- C08K3/34—Silicon-containing compounds
- C08K3/36—Silica
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Nanotechnology (AREA)
- Paints Or Removers (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Laminated Bodies (AREA)
- Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
- Polymerisation Methods In General (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
Abstract
Description
カラム ; 東ソー株式会社製ガードカラムHXL−H
+東ソー株式会社製 TSKgel G5000HXL
+東ソー株式会社製 TSKgel G4000HXL
+東ソー株式会社製 TSKgel G3000HXL
+東ソー株式会社製 TSKgel G2000HXL
検出器 ; RI(示差屈折計)
データ処理:東ソー株式会社製 SC−8010
測定条件: カラム温度 40℃
溶媒 テトラヒドロフラン
流速 1.0ml/分
標準 ;ポリスチレン
試料 ;樹脂固形分換算で0.4質量%のテトラヒドロフラン溶液をマイクロフィルターでろ過したもの(100μl)
前記アクリル重合体(X1)の原料となる前記アクリル重合体(Y1)は、前記エポキシ基と(メタ)アクリロイル基とを有する化合物(y1)の単独重合体でも良いし、他の重合性化合物(v1)との共重合体でも良い。
前記アクリル重合体(X2)の原料となる前記アクリル重合体(Y2)は、前記カルボキシル基と(メタ)アクリロイル基とを有する化合物(y2)の単独重合体でも良いし、他の重合性化合物(v2)との共重合体でも良い。
前記アクリル重合体(X3)の原料となる前記アクリル重合体(Y3)は、前記水酸基と(メタ)アクリロイル基とを有する化合物(y3)の単独重合体でも良いし、他の重合性化合物(v3)との共重合体でも良い。
カラム ; 東ソー株式会社製ガードカラムHXL−H
+東ソー株式会社製 TSKgel G5000HXL
+東ソー株式会社製 TSKgel G4000HXL
+東ソー株式会社製 TSKgel G3000HXL
+東ソー株式会社製 TSKgel G2000HXL
検出器 ; RI(示差屈折計)
データ処理:東ソー株式会社製 SC−8010
測定条件: カラム温度 40℃
溶媒 テトラヒドロフラン
流速 1.0ml/分
標準 ;ポリスチレン
試料 ;樹脂固形分換算で0.4質量%のテトラヒドロフラン溶液をマイクロフィルターでろ過したもの(100μl)
撹拌装置、冷却管、滴下ロートおよび窒素導入管を備えた反応装置に、メチルイソブチルケトン453質量部を仕込み、撹拌しながら系内温度が110℃になるまで昇温し、次いで、グリシジルメタアクリレート720質量部、メチルメタアクリレート480質量部およびt−ブチルパーオキシ−2−エチルヘキサノエート(日本乳化剤株式会社製「パーブチルO」)48質量部からなる混合液を3時間かけて滴下ロートより滴下した後、110℃で15時間保持した。次いで、90℃まで降温した後、メトキノン1.6質量部およびアクリル酸367質量部を仕込んだ後、トリフェニルホスフィン7.8質量部を添加後、さらに100℃まで昇温して8時間保持し、アクリル重合体(X−1)のメチルイソブチルケトン溶液3000質量部(不揮発分50.0質量%)を得た。該アクリル重合体(X−1)の各性状値は以下のようであった。重量平均分子量(Mw):13,000、固形分換算の理論アクリロイル基当量:321g/eq、水酸基価108mgKOH/g
撹拌装置を備えた反応装置にジシクロヘキシルメタン−4,4’−ジイソシアネート166質量部、ジブチル錫ジラウリート0.2質量部及びメトキノン0.2質量部を加え、攪拌しながら60℃まで昇温した。次いで、ペンタエリスリトールトリアクリレート(東亞合成株式会社製「アロニクスM−305」)630質量部を10回に分けて10分毎に仕込んだ。更に10時間反応させ、赤外線スペクトルで22500cm−1のイソシアネート基の吸収が消失したことを確認して反応を終了し、ウレタンアクリレート(B−1)を得た。該ウレタンアクリレート(B−1)の各性状値は以下のようであった。重量平均分子量(Mw):1,400、理論アクリロイル基当量:120g/eq
前記合成例1で得たアクリル重合体(X−1)のメチルイソブチルケトン溶液40質量部(アクリル重合体(X−1)は20.0質量部)、多官能アクリレートモノマー(東亞合成株式会社製「アロニックスM−404」)30質量部、疎水化処理した湿式法シリカ微粒子(A−1)(東ソー・シリカ株式会社製、ポリジメチルシロキサン処理、湿式法シリカ粒子、SS−50F)50質量部、メチルイソブチルケトン(以下「MIBK」と略記する)80質量部配合し、不揮発分50質量%のスラリーとしたものを、湿式ボールミル(アシザワ株式会社製「スターミルLMZ015」)を用いて混合分散し、分散体を得た。
メディア:メジアン径100μmのジルコニアビーズ
ミルの内容積に対する樹脂組成物の充填率:70体積%
攪拌翼の先端部の周速:11m/sec
樹脂組成物の流速:200ml/min
分散時間:60分
得られた分散体中の平均粒子径を、粒子径測定装置(大塚電子株式会社製「ELSZ−2」)を用いて測定した。
1.試験片の作製方法
前記活性エネルギー線硬化性樹脂組成物を、下記プラスチックフィルム上に、硬化後の膜厚がそれぞれ所定の値となるようにバーコーターで塗布し、70℃で1分乾燥させ、窒素下で高圧水銀灯を用いて250mJ/cm2の照射量で通過させて硬化させることにより、硬化塗膜を有する試験片を得た。
・ポリエチレンテレフタレートフィルム(以下「PET」と略記する)(膜厚125μm)上、5μm
・トリアセチルセルロースフィルム(以下「TAC」と略記する)(膜厚60μm)上、5μm
上記試験片の硬化塗膜をJIS K 5400に従い、ポリエチレンテレフタレートフィルムを基材とするものについては荷重750g、トリアセチルセルロールフィルムを基材とするものについては荷重500gの鉛筆引っかき試験によって評価した。5回試験を行い、1回以上傷がついた硬度の一つ下の硬度を、その塗膜の鉛筆硬度とした。
1.硬化塗膜の作製方法
前記活性エネルギー線硬化性樹脂組成物を、下記プラスチックフィルム上に、硬化後の膜厚がそれぞれ所定の値となるようにバーコーターで塗布し、70℃で1分乾燥させ、窒素下で高圧水銀灯を用いて250mJ/cm2の照射量で通過させて硬化させることにより、硬化塗膜を有する試験片を得た。
・ポリエチレンテレフタレートフィルム(以下「PET」と略記する)(膜厚75μm)上、3μm
スガ試験機株式会社製「ヘーズコンピュータHZ−2」を用いて塗膜のヘーズ値を測定した。ヘーズ値が低いほど塗膜の透明性は高い。
1.硬化塗膜の作製方法
前記活性エネルギー線硬化性樹脂組成物を、下記プラスチックフィルム上に、硬化後の膜厚がそれぞれ所定の値となるようにバーコーターで塗布し、70℃で1分乾燥させ、窒素下で高圧水銀灯を用いて250mJ/cm2の照射量で通過させて硬化させることにより、硬化塗膜を有する試験片を得た。
・ポリエチレンテレフタレートフィルム(以下「PET」と略記する)(膜厚75μm)上、5μm
試験片を10cm四方に切り、4角の水平からの浮きを測定し、その平均値で評価した。値が小さいほどカールが小さく、耐カール性に優れた塗膜である。
1.硬化塗膜の作製方法
前記活性エネルギー線硬化性樹脂組成物を、下記プラスチックフィルム上に、硬化後の膜厚がそれぞれ所定の値となるようにバーコーターで塗布し、70℃で1分乾燥させ、窒素下で高圧水銀灯を用いて250mJ/cm2の照射量で通過させて硬化させることにより、硬化塗膜を有する試験片を得た。
・ポリエチレンテレフタレートフィルム(以下「PET」と略記する)(膜厚75μm)上、3μm
汎用紫外線硬化型樹脂(例:ユニディック 17−806、DIC株式会社製)が塗装されている塗膜と上記試験片の塗装面とを合わせ荷重をかけて擦り合わせ、スムーズに滑る場合(アンチブロッキング性がある)〇、滑らない場合(ブロッキングする)×と判定した。
組成を表1に示す配合とした以外は実施例1と同様にして活性エネルギー線硬化性樹脂組成物を得た。これらについて実施例1と同様の試験を行った。結果を表1に示す。
尚、組成物中の各成分は、以下の通りである。
・シリカ微粒子(A−2):東ソー・シリカ株式会社製、ポリジメチルシロキサン処理湿式法シリカ微粒子「SAZ−20B」
前記合成例1で得たアクリル重合体(X−1)のMIBK溶液40質量部(アクリル重合体(X−1)は20.0質量部)、アロニックスM−404は30質量部、シリカ微粒子(A’−1)50質量部(EVONIK社製、疎水性フュームドシリカ AEROSIL R7200)、MIBK80質量部を配合し、不揮発分50質量%のスラリーとしたものを、湿式ボールミル(アシザワ株式会社製「スターミルLMZ015」)を用いて混合分散し、分散体を得た。該分散体について実施例1と同様に活性エネルギー線硬化性樹脂組成物を調製し、実施例1と同様の試験を行った。結果を表2に示す
メディア:メジアン径100μmのジルコニアビーズ
ミルの内容積に対する樹脂組成物の充填率:70体積%
攪拌翼の先端部の周速:11m/sec
樹脂組成物の流速:200ml/min
分散時間:40分
得られた分散体中の平均粒子径を、粒子径測定装置(大塚電子株式会社製「ELSZ−2」)を用いて測定した。
組成を表2に示す配合とした以外は比較例1と同様にして活性エネルギー線硬化性樹脂組成物を調整し、実施例1と同様の試験を行った。結果を表2に示す。
・シリカ微粒子(A’−2):(EVONIK社製、疎水性フュームドシリカ AEROSIL R8200)
前記合成例1で得たアクリル重合体(X−1)のMIBK溶液40質量部(アクリル重合体(X−1)は20.0質量部)、アロニックスM−404 30質量部、シリカ微粒子(A’−3)50質量部(東ソー・シリカ株式会社製、未処理沈殿法シリカ粒子、E−220A)、オルガノポリシロキサン5質量部、MIBK80質量部を配合し、不揮発分50質量%のスラリーとしたものを、湿式ボールミル(アシザワ株式会社製「スターミルLMZ015」)を用いて混合分散し、分散体を得た。該分散体について比較例1と同様に活性エネルギー線硬化性樹脂組成物を調製し、実施例1と同様の試験を行った。結果を表2に示す。
メディア:メジアン径100μmのジルコニアビーズ
ミルの内容積に対する樹脂組成物の充填率:70体積%
攪拌翼の先端部の周速:11m/sec
樹脂組成物の流速:200ml/min
分散時間:90分
得られた分散体中の平均粒子径を、粒子径測定装置(大塚電子株式会社製「ELSZ−2」)を用いて測定した。
Claims (11)
- 疎水化処理した湿式法シリカ微粒子(A)と、(メタ)アクリロイル基を有する化合物(B)とを含有し、前記湿式法シリカ微粒子(A)の平均粒子径が90〜130nmの範囲で分散されたものであることを特徴とする活性エネルギー線硬化性樹脂組成物。
- 前記疎水化処理が、湿式法で得られたシリカ微粒子の表面をポリジメチルシロキサンで処理したものである請求項1記載の活性エネルギー線硬化性樹脂組成物。
- 前記活性エネルギー線硬化性樹脂組成物中の不揮発分100質量部中に、前記疎水化処理した湿式法シリカ微粒子(A)を5〜80質量部の範囲で含有するものである請求項1又は2記載の活性エネルギー線硬化性樹脂組成物。
- 前記(メタ)アクリロイル基を有する化合物(B)が、重量平均分子量(Mw)が3,000〜80,000の範囲の分子構造中に(メタ)アクリロイル基を有するアクリル重合体(X)である請求項1〜3の何れか1項記載の活性エネルギー線硬化性樹脂組成物。
- 前記アクリル重合体(X)の(メタ)アクリロイル基当量が220〜1650eq/gの範囲である請求項4記載の活性エネルギー線硬化性樹脂組成物。
- 前記アクリル重合体(X)が分子構造中に水酸基を有し、その水酸基当量が35〜250mgKOH/gの範囲である請求項4又は5記載の活性エネルギー線硬化性樹脂組成物。
- 前記(メタ)アクリロイル基を有する化合物(B)が、2官能以上の(メタ)アクリレート単量体である請求項1〜3の何れか1項記載の活性エネルギー線硬化性樹脂組成物。
- 請求項1〜7の何れか一つ記載の活性エネルギー線硬化性樹脂組成物を含有することを特徴とする塗料。
- 請求項8記載の塗料を硬化させてなることを特徴とする塗膜。
- 請求項9記載の塗膜をプラスチックフィルムの片面又は両面に有することを特徴とする積層フィルム。
- 前記塗膜の膜厚が0.1〜100μmの範囲である請求項10記載の積層フィルム。
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Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03258866A (ja) * | 1990-03-07 | 1991-11-19 | Nippon Sheet Glass Co Ltd | ポリジメチルシロキサン被覆微粒子 |
JP2004250741A (ja) * | 2003-02-19 | 2004-09-09 | Nippon Paint Co Ltd | 雪止め金具の塗装方法、および塗装された雪止め金具 |
JP2011201938A (ja) * | 2010-03-24 | 2011-10-13 | Dic Corp | 無機粒子分散体、エネルギー線硬化性樹脂組成物、及びフィルム |
WO2012176570A1 (ja) * | 2011-06-24 | 2012-12-27 | Dic株式会社 | 活性エネルギー線硬化型樹脂組成物、活性エネルギー線硬化型樹脂組成物の製造方法、塗料、塗膜、及びフィルム |
JP2013163786A (ja) * | 2012-02-13 | 2013-08-22 | Asahi Kasei E-Materials Corp | 感光性シリコーン樹脂組成物 |
JP2014152191A (ja) * | 2013-02-05 | 2014-08-25 | Denki Kagaku Kogyo Kk | エネルギー線硬化性樹脂組成物 |
WO2014192654A1 (ja) * | 2013-05-28 | 2014-12-04 | Dic株式会社 | 活性エネルギー線硬化性組成物及びそれを用いたフィルム |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3133041B2 (ja) * | 1989-04-03 | 2001-02-05 | エイ・ジイ・インタナショナル・ケミカル株式会社 | 繊維強化熱硬化性樹脂成形物の製造方法 |
US20090234072A1 (en) * | 2005-09-08 | 2009-09-17 | Kaneka Corporation | Curable composition |
JP2008062539A (ja) | 2006-09-08 | 2008-03-21 | Nakajima Kogyo Kk | 防眩フィルム |
JP5407114B2 (ja) | 2006-03-30 | 2014-02-05 | 荒川化学工業株式会社 | 反応性分散体を含有する活性エネルギー線硬化型コーティング剤組成物、反応性分散体の製造方法および硬化被膜 |
JP5504605B2 (ja) * | 2007-10-30 | 2014-05-28 | 大日本印刷株式会社 | ハードコート層用硬化性樹脂組成物、及びハードコートフィルム |
JP2010100817A (ja) | 2008-09-26 | 2010-05-06 | Dic Corp | コーティング用活性エネルギー線硬化型樹脂組成物及びフィルム基材 |
CN103842396B (zh) * | 2011-09-30 | 2016-03-16 | Dic株式会社 | 活性能量射线固化型树脂组合物、其制造方法、涂料、涂膜和薄膜 |
JP5858278B2 (ja) | 2011-11-22 | 2016-02-10 | Dic株式会社 | 活性エネルギー線硬化型樹脂組成物、活性エネルギー線硬化型樹脂組成物の製造方法、塗料、塗膜、及びフィルム |
JP6180077B2 (ja) * | 2012-03-23 | 2017-08-16 | 関西ペイント株式会社 | 活性エネルギー線硬化性組成物及び塗装フィルム |
US9447294B2 (en) * | 2012-06-19 | 2016-09-20 | Natoco Co., Ltd. | Active energy ray curable composition, and cured product and use thereof |
-
2015
- 2015-11-12 JP JP2016514186A patent/JP6032383B1/ja active Active
- 2015-11-12 KR KR1020177012450A patent/KR102406434B1/ko active IP Right Grant
- 2015-11-12 US US15/537,876 patent/US20170368806A1/en not_active Abandoned
- 2015-11-12 CN CN201580067286.8A patent/CN107001496B/zh active Active
- 2015-11-12 WO PCT/JP2015/081843 patent/WO2016103957A1/ja active Application Filing
- 2015-12-11 TW TW104141640A patent/TWI689539B/zh active
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03258866A (ja) * | 1990-03-07 | 1991-11-19 | Nippon Sheet Glass Co Ltd | ポリジメチルシロキサン被覆微粒子 |
JP2004250741A (ja) * | 2003-02-19 | 2004-09-09 | Nippon Paint Co Ltd | 雪止め金具の塗装方法、および塗装された雪止め金具 |
JP2011201938A (ja) * | 2010-03-24 | 2011-10-13 | Dic Corp | 無機粒子分散体、エネルギー線硬化性樹脂組成物、及びフィルム |
WO2012176570A1 (ja) * | 2011-06-24 | 2012-12-27 | Dic株式会社 | 活性エネルギー線硬化型樹脂組成物、活性エネルギー線硬化型樹脂組成物の製造方法、塗料、塗膜、及びフィルム |
JP2013163786A (ja) * | 2012-02-13 | 2013-08-22 | Asahi Kasei E-Materials Corp | 感光性シリコーン樹脂組成物 |
JP2014152191A (ja) * | 2013-02-05 | 2014-08-25 | Denki Kagaku Kogyo Kk | エネルギー線硬化性樹脂組成物 |
WO2014192654A1 (ja) * | 2013-05-28 | 2014-12-04 | Dic株式会社 | 活性エネルギー線硬化性組成物及びそれを用いたフィルム |
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CN107001496A (zh) | 2017-08-01 |
TWI689539B (zh) | 2020-04-01 |
TW201629134A (zh) | 2016-08-16 |
KR20170101189A (ko) | 2017-09-05 |
US20170368806A1 (en) | 2017-12-28 |
WO2016103957A1 (ja) | 2016-06-30 |
CN107001496B (zh) | 2019-12-10 |
JPWO2016103957A1 (ja) | 2017-04-27 |
KR102406434B1 (ko) | 2022-06-08 |
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