JP6870930B2 - 表面保護フィルム - Google Patents
表面保護フィルム Download PDFInfo
- Publication number
- JP6870930B2 JP6870930B2 JP2016133099A JP2016133099A JP6870930B2 JP 6870930 B2 JP6870930 B2 JP 6870930B2 JP 2016133099 A JP2016133099 A JP 2016133099A JP 2016133099 A JP2016133099 A JP 2016133099A JP 6870930 B2 JP6870930 B2 JP 6870930B2
- Authority
- JP
- Japan
- Prior art keywords
- meth
- sensitive adhesive
- pressure
- adhesive layer
- base material
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 230000001681 protective effect Effects 0.000 title claims description 82
- 239000004820 Pressure-sensitive adhesive Substances 0.000 claims description 169
- 239000010410 layer Substances 0.000 claims description 120
- 239000000178 monomer Substances 0.000 claims description 113
- 239000000463 material Substances 0.000 claims description 106
- 229920000058 polyacrylate Polymers 0.000 claims description 87
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 35
- 229920000728 polyester Polymers 0.000 claims description 23
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 17
- 239000000758 substrate Substances 0.000 claims description 11
- 239000012790 adhesive layer Substances 0.000 claims description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 78
- 239000000203 mixture Substances 0.000 description 57
- -1 polyethylene terephthalate Polymers 0.000 description 56
- 239000003999 initiator Substances 0.000 description 38
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 28
- 239000003431 cross linking reagent Substances 0.000 description 28
- 229910052757 nitrogen Inorganic materials 0.000 description 23
- 239000003505 polymerization initiator Substances 0.000 description 21
- 239000004611 light stabiliser Substances 0.000 description 17
- 206010040844 Skin exfoliation Diseases 0.000 description 16
- 239000006096 absorbing agent Substances 0.000 description 15
- 125000004433 nitrogen atom Chemical group N* 0.000 description 15
- 239000000853 adhesive Substances 0.000 description 14
- 230000001070 adhesive effect Effects 0.000 description 14
- 239000002904 solvent Substances 0.000 description 14
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 14
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 13
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 12
- 125000000217 alkyl group Chemical group 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 12
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- 125000002723 alicyclic group Chemical group 0.000 description 10
- 238000000034 method Methods 0.000 description 10
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- 239000012986 chain transfer agent Substances 0.000 description 9
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- 229920000139 polyethylene terephthalate Polymers 0.000 description 9
- 239000005020 polyethylene terephthalate Substances 0.000 description 9
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 8
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 8
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- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 7
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- 150000001412 amines Chemical class 0.000 description 7
- 125000003118 aryl group Chemical group 0.000 description 7
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 7
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- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 6
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- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 6
- 239000007795 chemical reaction product Substances 0.000 description 6
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- 238000004519 manufacturing process Methods 0.000 description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
- 239000005056 polyisocyanate Substances 0.000 description 6
- 229920001228 polyisocyanate Polymers 0.000 description 6
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 6
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 5
- 239000007983 Tris buffer Substances 0.000 description 5
- 239000012964 benzotriazole Substances 0.000 description 5
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 5
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- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 4
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- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 4
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- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 238000004132 cross linking Methods 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 235000019382 gum benzoic Nutrition 0.000 description 4
- 239000012948 isocyanate Substances 0.000 description 4
- 150000002513 isocyanates Chemical class 0.000 description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- 230000000379 polymerizing effect Effects 0.000 description 4
- 239000004814 polyurethane Substances 0.000 description 4
- 229920002635 polyurethane Polymers 0.000 description 4
- 238000012719 thermal polymerization Methods 0.000 description 4
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 4
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical class CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 4
- 238000002834 transmittance Methods 0.000 description 4
- 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 4
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 4
- RSJKGSCJYJTIGS-UHFFFAOYSA-N undecane Chemical compound CCCCCCCCCCC RSJKGSCJYJTIGS-UHFFFAOYSA-N 0.000 description 4
- 229920002554 vinyl polymer Polymers 0.000 description 4
- KWVGIHKZDCUPEU-UHFFFAOYSA-N 2,2-dimethoxy-2-phenylacetophenone Chemical compound C=1C=CC=CC=1C(OC)(OC)C(=O)C1=CC=CC=C1 KWVGIHKZDCUPEU-UHFFFAOYSA-N 0.000 description 3
- OLFNXLXEGXRUOI-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4,6-bis(2-phenylpropan-2-yl)phenol Chemical compound C=1C(N2N=C3C=CC=CC3=N2)=C(O)C(C(C)(C)C=2C=CC=CC=2)=CC=1C(C)(C)C1=CC=CC=C1 OLFNXLXEGXRUOI-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- NLGDWWCZQDIASO-UHFFFAOYSA-N 2-hydroxy-1-(7-oxabicyclo[4.1.0]hepta-1,3,5-trien-2-yl)-2-phenylethanone Chemical compound OC(C(=O)c1cccc2Oc12)c1ccccc1 NLGDWWCZQDIASO-UHFFFAOYSA-N 0.000 description 3
- VMRIVYANZGSGRV-UHFFFAOYSA-N 4-phenyl-2h-triazin-5-one Chemical compound OC1=CN=NN=C1C1=CC=CC=C1 VMRIVYANZGSGRV-UHFFFAOYSA-N 0.000 description 3
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 3
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
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- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 3
- 125000002619 bicyclic group Chemical group 0.000 description 3
- FQUNFJULCYSSOP-UHFFFAOYSA-N bisoctrizole Chemical compound N1=C2C=CC=CC2=NN1C1=CC(C(C)(C)CC(C)(C)C)=CC(CC=2C(=C(C=C(C=2)C(C)(C)CC(C)(C)C)N2N=C3C=CC=CC3=N2)O)=C1O FQUNFJULCYSSOP-UHFFFAOYSA-N 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
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- 229910052751 metal Inorganic materials 0.000 description 3
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- PJUIMOJAAPLTRJ-UHFFFAOYSA-N monothioglycerol Chemical compound OCC(O)CS PJUIMOJAAPLTRJ-UHFFFAOYSA-N 0.000 description 3
- NWAHZAIDMVNENC-UHFFFAOYSA-N octahydro-1h-4,7-methanoinden-5-yl methacrylate Chemical compound C12CCCC2C2CC(OC(=O)C(=C)C)C1C2 NWAHZAIDMVNENC-UHFFFAOYSA-N 0.000 description 3
- 150000002923 oximes Chemical class 0.000 description 3
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- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 3
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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 2
- HNURKXXMYARGAY-UHFFFAOYSA-N 2,6-Di-tert-butyl-4-hydroxymethylphenol Chemical compound CC(C)(C)C1=CC(CO)=CC(C(C)(C)C)=C1O HNURKXXMYARGAY-UHFFFAOYSA-N 0.000 description 2
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- UZUNCLSDTUBVCN-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-6-(2-phenylpropan-2-yl)-4-(2,4,4-trimethylpentan-2-yl)phenol Chemical compound C=1C(C(C)(C)CC(C)(C)C)=CC(N2N=C3C=CC=CC3=N2)=C(O)C=1C(C)(C)C1=CC=CC=C1 UZUNCLSDTUBVCN-UHFFFAOYSA-N 0.000 description 2
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- HXDOZKJGKXYMEW-UHFFFAOYSA-N 4-ethylphenol Chemical compound CCC1=CC=C(O)C=C1 HXDOZKJGKXYMEW-UHFFFAOYSA-N 0.000 description 2
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- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
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- 125000001931 aliphatic group Chemical group 0.000 description 2
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- 125000001204 arachidyl 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])C([H])([H])C([H])([H])[H] 0.000 description 2
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- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
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- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
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- 125000002960 margaryl 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])[H] 0.000 description 2
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 2
- 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 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- 239000012299 nitrogen atmosphere Substances 0.000 description 2
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- UJRDRFZCRQNLJM-UHFFFAOYSA-N methyl 3-[3-(benzotriazol-2-yl)-5-tert-butyl-4-hydroxyphenyl]propanoate Chemical compound CC(C)(C)C1=CC(CCC(=O)OC)=CC(N2N=C3C=CC=CC3=N2)=C1O UJRDRFZCRQNLJM-UHFFFAOYSA-N 0.000 description 1
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- JAYXSROKFZAHRQ-UHFFFAOYSA-N n,n-bis(oxiran-2-ylmethyl)aniline Chemical compound C1OC1CN(C=1C=CC=CC=1)CC1CO1 JAYXSROKFZAHRQ-UHFFFAOYSA-N 0.000 description 1
- KBJFYLLAMSZSOG-UHFFFAOYSA-N n-(3-trimethoxysilylpropyl)aniline Chemical compound CO[Si](OC)(OC)CCCNC1=CC=CC=C1 KBJFYLLAMSZSOG-UHFFFAOYSA-N 0.000 description 1
- OPECTNGATDYLSS-UHFFFAOYSA-N naphthalene-2-sulfonyl chloride Chemical compound C1=CC=CC2=CC(S(=O)(=O)Cl)=CC=C21 OPECTNGATDYLSS-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 229920006113 non-polar polymer Polymers 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
- MDYPDLBFDATSCF-UHFFFAOYSA-N nonyl prop-2-enoate Chemical compound CCCCCCCCCOC(=O)C=C MDYPDLBFDATSCF-UHFFFAOYSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- KZCOBXFFBQJQHH-UHFFFAOYSA-N octane-1-thiol Chemical compound CCCCCCCCS KZCOBXFFBQJQHH-UHFFFAOYSA-N 0.000 description 1
- MADOXCFISYCULS-UHFFFAOYSA-N octyl 2-sulfanylacetate Chemical compound CCCCCCCCOC(=O)CS MADOXCFISYCULS-UHFFFAOYSA-N 0.000 description 1
- DMFXLIFZVRXRRR-UHFFFAOYSA-N octyl 3-[3-tert-butyl-5-(5-chlorobenzotriazol-2-yl)-4-hydroxyphenyl]propanoate Chemical compound CC(C)(C)C1=CC(CCC(=O)OCCCCCCCC)=CC(N2N=C3C=C(Cl)C=CC3=N2)=C1O DMFXLIFZVRXRRR-UHFFFAOYSA-N 0.000 description 1
- AXRSHKZFNKUGQB-UHFFFAOYSA-N octyl diphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OCCCCCCCC)OC1=CC=CC=C1 AXRSHKZFNKUGQB-UHFFFAOYSA-N 0.000 description 1
- ZDHCZVWCTKTBRY-UHFFFAOYSA-N omega-Hydroxydodecanoic acid Natural products OCCCCCCCCCCCC(O)=O ZDHCZVWCTKTBRY-UHFFFAOYSA-N 0.000 description 1
- REJKHFKLPFJGAQ-UHFFFAOYSA-N oxiran-2-ylmethanethiol Chemical compound SCC1CO1 REJKHFKLPFJGAQ-UHFFFAOYSA-N 0.000 description 1
- DXGLGDHPHMLXJC-UHFFFAOYSA-N oxybenzone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 DXGLGDHPHMLXJC-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen 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
- 239000003208 petroleum Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- YKEAZOGAZWPICS-UHFFFAOYSA-N phenyl 2-hydroxy-3-methoxybenzoate Chemical compound COC1=CC=CC(C(=O)OC=2C=CC=CC=2)=C1O YKEAZOGAZWPICS-UHFFFAOYSA-N 0.000 description 1
- YEBPMWUBZDANBU-UHFFFAOYSA-N phenyl 2-hydroxy-3-methylbenzoate Chemical compound CC1=CC=CC(C(=O)OC=2C=CC=CC=2)=C1O YEBPMWUBZDANBU-UHFFFAOYSA-N 0.000 description 1
- HFZCMVHAJOXWIY-UHFFFAOYSA-N phenyl 2-hydroxy-4-methylbenzoate Chemical compound OC1=CC(C)=CC=C1C(=O)OC1=CC=CC=C1 HFZCMVHAJOXWIY-UHFFFAOYSA-N 0.000 description 1
- AMLDDICCKSCSQI-UHFFFAOYSA-N phenyl 2-hydroxy-5-methylbenzoate Chemical compound CC1=CC=C(O)C(C(=O)OC=2C=CC=CC=2)=C1 AMLDDICCKSCSQI-UHFFFAOYSA-N 0.000 description 1
- KTOUIDNVCQYAQQ-UHFFFAOYSA-N phenyl 2-prop-2-enoyloxybenzoate Chemical compound C=CC(=O)OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 KTOUIDNVCQYAQQ-UHFFFAOYSA-N 0.000 description 1
- VBJPJCCADDYOSB-UHFFFAOYSA-N phenyl 3-methoxy-2-prop-2-enoyloxybenzoate Chemical compound COC1=CC=CC(C(=O)OC=2C=CC=CC=2)=C1OC(=O)C=C VBJPJCCADDYOSB-UHFFFAOYSA-N 0.000 description 1
- ABLABINHTJNBGN-UHFFFAOYSA-N phenyl 3-methyl-2-prop-2-enoyloxybenzoate Chemical compound CC1=CC=CC(C(=O)OC=2C=CC=CC=2)=C1OC(=O)C=C ABLABINHTJNBGN-UHFFFAOYSA-N 0.000 description 1
- VLRWXGSSRJIRIJ-UHFFFAOYSA-N phenyl 4-methyl-2-prop-2-enoyloxybenzoate Chemical compound C=CC(=O)OC1=CC(C)=CC=C1C(=O)OC1=CC=CC=C1 VLRWXGSSRJIRIJ-UHFFFAOYSA-N 0.000 description 1
- VHDQRJJAZGSSIV-UHFFFAOYSA-N phenyl 5-methyl-2-prop-2-enoyloxybenzoate Chemical compound CC1=CC=C(OC(=O)C=C)C(C(=O)OC=2C=CC=CC=2)=C1 VHDQRJJAZGSSIV-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000009832 plasma treatment Methods 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920003207 poly(ethylene-2,6-naphthalate) Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229940068886 polyethylene glycol 300 Drugs 0.000 description 1
- 239000011112 polyethylene naphthalate Substances 0.000 description 1
- 229920000223 polyglycerol Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 150000003097 polyterpenes Chemical class 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- YHPUTXNFABTCGG-UHFFFAOYSA-N propyl 2-sulfanylacetate Chemical compound CCCOC(=O)CS YHPUTXNFABTCGG-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
- 150000003254 radicals Chemical class 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229940116351 sebacate Drugs 0.000 description 1
- CXMXRPHRNRROMY-UHFFFAOYSA-L sebacate(2-) Chemical compound [O-]C(=O)CCCCCCCCC([O-])=O CXMXRPHRNRROMY-UHFFFAOYSA-L 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- CXVGEDCSTKKODG-UHFFFAOYSA-N sulisobenzone Chemical compound C1=C(S(O)(=O)=O)C(OC)=CC(O)=C1C(=O)C1=CC=CC=C1 CXVGEDCSTKKODG-UHFFFAOYSA-N 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- YXIMCNGUIIEJMO-UHFFFAOYSA-N tert-butyl 2-sulfanylacetate Chemical compound CC(C)(C)OC(=O)CS YXIMCNGUIIEJMO-UHFFFAOYSA-N 0.000 description 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- LVEOKSIILWWVEO-UHFFFAOYSA-N tetradecyl 3-(3-oxo-3-tetradecoxypropyl)sulfanylpropanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCCCC LVEOKSIILWWVEO-UHFFFAOYSA-N 0.000 description 1
- 235000010384 tocopherol Nutrition 0.000 description 1
- 229960001295 tocopherol Drugs 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 238000012546 transfer Methods 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
- QQBLOZGVRHAYGT-UHFFFAOYSA-N tris-decyl phosphite Chemical compound CCCCCCCCCCOP(OCCCCCCCCCC)OCCCCCCCCCC QQBLOZGVRHAYGT-UHFFFAOYSA-N 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/20—Adhesives in the form of films or foils characterised by their carriers
- C09J7/22—Plastics; Metallised plastics
- C09J7/25—Plastics; Metallised plastics based on macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
- C09J7/255—Polyesters
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J133/00—Adhesives 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; Adhesives based on derivatives of such polymers
- C09J133/04—Homopolymers or copolymers of esters
- C09J133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09J133/062—Copolymers with monomers not covered by C09J133/06
- C09J133/066—Copolymers with monomers not covered by C09J133/06 containing -OH groups
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
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- C09J133/00—Adhesives 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; Adhesives based on derivatives of such polymers
- C09J133/24—Homopolymers or copolymers of amides or imides
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J135/00—Adhesives 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 a carboxyl radical, and containing at least another carboxyl radical in the molecule, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Adhesives based on derivatives of such polymers
- C09J135/02—Homopolymers or copolymers of esters
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
- C09J7/38—Pressure-sensitive adhesives [PSA]
- C09J7/381—Pressure-sensitive adhesives [PSA] based on macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- C09J7/385—Acrylic polymers
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2301/00—Additional features of adhesives in the form of films or foils
- C09J2301/30—Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier
- C09J2301/312—Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier parameters being the characterizing feature
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Adhesive Tapes (AREA)
- Laminated Bodies (AREA)
- Physics & Mathematics (AREA)
- Materials For Medical Uses (AREA)
- General Physics & Mathematics (AREA)
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Description
・カラム:TSKgel SuperAWM-H(上流側,東ソー株式会社製)とTSKgel SuperAW4000(東ソー株式会社製)とTSKgel SuperAW2500(下流側,東ソー株式会社製)とを直列に接続
・カラムサイズ:各カラムとも6.0mmφ×150mm
・カラム温度(測定温度):40℃
・溶離液:テトラヒドロフラン(THF)
・流量:0.4mL/分
・サンプル注入量:20μL
・サンプル濃度:約2.0g/L(テトラヒドロフラン溶液)
・標準試料:ポリスチレン
・検出器:示差屈折計(RI)
反応容器内で、メタクリル酸ジシクロペンタニル(DCPMA)60重量部と、メタクリル酸メチル(MMA)40重量部と、連鎖移動剤としてのα-チオグリセロール3.5重量部と、重合溶媒としてのトルエン100重量部とを含む混合物を、70℃で1時間、窒素雰囲気下で撹拌した。次に、重合開始剤としての2,2'-アゾビスイソブチロニトリル0.2重量部を反応容器内の混合物に加えて反応溶液を調製し、70℃で2時間、反応を行った。続いて、80℃で2時間、反応を行った。その後、反応容器内の反応溶液を、130℃の温度雰囲気下に置き、当該反応溶液からトルエン、連鎖移動剤、および未反応モノマーを乾燥除去した。これにより、固形状のアクリル系オリゴマーを得た。当該アクリル系オリゴマーの重量平均分子量(Mw)は、5.1×103であった。
アクリル酸2-エチルヘキシル(2EHA)78重量部と、N-ビニル-2-ピロリドン(NVP)18重量部と、アクリル酸2-ヒドロキシエチル(HEA)4重量部とを含有するモノマー混合物に、第1の光重合開始剤(商品名「イルガキュア651」,BASF社製)0.035重量部および第2の光重合開始剤(商品名「イルガキュア184」,BASF社製)0.035重量部を加えた後、当該混合物に対し、粘度測定装置を使用して粘度を測定しつつ当該混合物の粘度が約20Pa・sになるまで紫外線照射装置を使用して紫外線を照射した。粘度測定において、装置のローター回転速度は10rpmとし、測定温度は30℃とした。これにより、混合物中のモノマー成分の一部が重合した部分重合物たるプレポリマー組成物(重合反応を経ていないモノマー成分を含有する)を得た。そして、このプレポリマー組成物100重量部と、上述のアクリル系オリゴマー11.8重量部と、アクリル酸2-ヒドロキシエチル(HEA)17.6重量部と、1,6-ヘキサンジオールジアクリレート(HDDA)0.294重量部と、シランカップリング剤(商品名「KBM-403」,信越化学工業株式会社製)0.353重量部とを混合した。これにより、アクリル系粘着剤組成物(アクリル系粘着剤組成物C1)を得た。
環流冷却器、窒素ガス導入管、攪拌機、および温度計を備え付けたフラスコ(反応容器)内で、アクリル酸2-エチルヘキシル(2EHA)100重量部と、アクリル酸2-ヒドロキシエチル(HEA)4重量部と、重合開始剤としての2,2'-アゾビスイソブチロニトリル0.2重量部と、重合溶媒としての酢酸エチル205重量部とを含む混合物を、窒素雰囲気下で穏やかに撹拌しつつ、63℃で4時間、反応を行った。これにより、約35重量%の濃度でアクリル系ポリマーを含有する溶液(アクリル系ポリマー溶液)を得た。そして、アクリル系ポリマー濃度が29重量%となるようにアクリル系ポリマー溶液を酢酸エチルで希釈した後、当該アクリル系ポリマー溶液に、アクリル系ポリマー100重量部に対して4重量部のトリメチロールプロパン/トリレンジイソシアネート付加物(商品名「コロネートL」,日本ポリウレタン工業株式会社製)と、0.02重量部の錫系触媒たるジオクチルスズジラウレート(商品名「エンビライザー OL-1」,東京ファインケミカル株式会社製)と、3重量部の架橋遅延剤たるアセチルアセトンとを加えて、25℃で約1分間の混合を行った。これにより、溶剤型のアクリル系粘着剤組成物(アクリル系粘着剤組成物C2)を得た。
厚さ80μmの第1のポリエチレンテレフタレートフィルム(商品名「コスモシャイン SRF」,面内位相差8400,東洋紡株式会社製)の両面にコロナ処理を施して得たフィルム(フィルムF1)の上に、上記のアクリル系粘着剤組成物C1を塗布し、粘着剤組成物層を形成した。次に、ポリエチレンテレフタレート(PET)系剥離ライナー(厚さ125μm,日東電工株式会社製)を当該粘着剤組成物層上に積層し、当該粘着剤組成物層を被覆して酸素を遮断した。このようにして、[剥離ライナー/粘着剤組成物層/フィルムF1]の積層構成を有する積層体を得た。次に、この積層体に対し、剥離ライナーの側から、ブラックライト(株式会社東芝製)を使用して照度3mW/cm2の紫外線を300秒間照射した。これによって積層体の粘着剤組成物層を硬化させて粘着剤層とした。この粘着剤層の厚さは100μmである。以上のようにして、[剥離ライナー/粘着剤層(厚さ100μm)/基材たるフィルムF1(厚さ80μm)]の積層構成を有する実施例1の表面保護フィルムを作製した。
厚さ80μmの第2のポリエチレンテレフタレートフィルムの両面にコロナ処理を施して得たフィルム(フィルムF2)の上に、上記のアクリル系粘着剤組成物C2を塗布し、粘着剤組成物層を形成した。第2のポリエチレンテレフタレートフィルムは、第1のポリエチレンテレフタレートフィルムたる「コスモシャイン SRF」の易接着処理層をハードコート用途の易接着処理層に替えた、東洋紡株式会社製のフィルムである。次に、この粘着剤組成物層を130℃で60秒間加熱して乾燥および硬化させ、フィルムF2上に粘着剤層を形成した。この粘着剤層の厚さは21μmである。そして、この粘着剤層の表面にPET系剥離ライナー(厚さ25μm,日東電工株式会社製)を貼り合わせた。以上のようにして、[剥離ライナー/粘着剤層(厚さ21μm)/基材たるフィルムF2(厚さ80μm)]の積層構成を有する実施例2の表面保護フィルムを作製した。
表面保護フィルムの基材として、厚さ75μmの第3のポリエチレンテレフタレートフィルム(商品名「XD500P」,面内位相差3000,東レ株式会社製)の両面にコロナ処理を施して得たフィルム(フィルムF3)をフィルムF1の代わりに用いたこと以外は実施例1と同様にして、比較例1の表面保護フィルムを作製した。
表面保護フィルムの基材としてフィルムF2に代えてフィルムF3を用いたこと以外は実施例2と同様にして、比較例2の表面保護フィルムを作製した。
実施例および比較例の表面保護フィルムから切り出された各サンプル片(60mm×75mm)について、エルメンドルフ引裂強度測定装置(商品名「エルメンドルフ引裂度試験機」,テスター産業株式会社製)を使用して、テープ基材の幅方向(TD)のエルメンドルフ引裂強度(N)とテープ基材の機械方向(MD)におけるエルメンドルフ引裂強度(N)とを、それぞれ測定した。本測定は、JIS K 7128−2に準拠して行った。測定に付されたサンプル片には、その端から測定方向(TDまたはMD)に延びる長さ20mmの切込みが予め設けられている。本測定では、当該切込みが更に伸びるように装置によってサンプル片に付与される引裂負荷に対する抵抗力が、測定される。また、本測定に使用した上記装置の計測最大値は1Nである。本測定の結果を表1に掲げる。
実施例および比較例の各表面保護フィルムについて、その基材幅方向の手切れ性を調べた。具体的には、剥離ライナーが剥離された表面保護フィルムについて、その基材幅方向への手作業による引裂きを試みた。当該手作業検査において、容易に引き裂くことが出来た場合を手切れ性は良好(○)と評価し、引き裂くことが出来なかった場合を手切れ性は不良(×)と評価した。その結果を表1に掲げる。
実施例および比較例の各表面保護フィルムについて、ヘーズメーター HM-150型(株式会社村上色彩技術研究所製)を使用して、JIS K 7136に規定の方法に準拠してヘーズ(%)を測定した。本測定は、剥離ライナーが剥離され且つスライドガラス(商品名「スライドグラス S1112」,厚さ1.0〜1.2mm,松波硝子工業株式会社製)に貼り付けられた状態にある表面保護フィルムについて行った。その結果を表1に掲げる。
本発明の構成を具備する実施例1,2の表面保護フィルムにおいては、いずれも、良好な手切れ性が実現された。これに対し、比較例1,2の表面保護フィルムにおいては、いずれも、基材幅方向に手で引き裂くことが出来ず、良好な手切れ性が実現されなかった。
11 基材
12 粘着剤層
Claims (2)
- 透明基材と粘着剤層とを含む積層構造を有する表面保護フィルムであって、
前記透明基材は、基材幅方向一軸延伸ポリエステル系基材であり且つ80μm以上125μm以下の厚さを有し、
前記粘着剤層は、アクリル系ポリマーにおける水酸基含有モノマー由来のモノマーユニットの割合が10重量%以上20重量%以下であるアクリル系粘着剤を含む粘着剤層であり且つ100μm以上1000μm以下の厚さを有し、
基材幅方向における表面保護フィルムのエルメンドルフ引裂強度が0.5N以下であり、且つ、基材機械方向における表面保護フィルムのエルメンドルフ引裂強度が1N以上である、表面保護フィルム。
- ヘーズが3%以下である、請求項1に記載の表面保護フィルム。
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