JP5307378B2 - (メタ)アクリル系フィルムおよびこれを用いたマーキングフィルム - Google Patents
(メタ)アクリル系フィルムおよびこれを用いたマーキングフィルム Download PDFInfo
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- JP5307378B2 JP5307378B2 JP2007279299A JP2007279299A JP5307378B2 JP 5307378 B2 JP5307378 B2 JP 5307378B2 JP 2007279299 A JP2007279299 A JP 2007279299A JP 2007279299 A JP2007279299 A JP 2007279299A JP 5307378 B2 JP5307378 B2 JP 5307378B2
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- meth
- acrylic
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- acrylic polymer
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- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 title claims abstract description 75
- 229920000058 polyacrylate Polymers 0.000 claims abstract description 78
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 32
- 125000003277 amino group Chemical group 0.000 claims abstract description 31
- 125000000524 functional group Chemical group 0.000 claims abstract description 20
- 239000003431 cross linking reagent Substances 0.000 claims abstract description 15
- 239000012790 adhesive layer Substances 0.000 claims description 14
- 230000009477 glass transition Effects 0.000 claims description 11
- 239000011241 protective layer Substances 0.000 claims description 11
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 239000000049 pigment Substances 0.000 claims 1
- 239000000178 monomer Substances 0.000 description 38
- 239000010410 layer Substances 0.000 description 28
- 229920000642 polymer Polymers 0.000 description 25
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 23
- 239000011347 resin Substances 0.000 description 18
- 229920005989 resin Polymers 0.000 description 18
- -1 buildings Substances 0.000 description 17
- 238000000034 method Methods 0.000 description 17
- 239000000243 solution Substances 0.000 description 17
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 15
- 239000000853 adhesive Substances 0.000 description 12
- 239000000203 mixture Substances 0.000 description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 11
- 230000001070 adhesive effect Effects 0.000 description 11
- 239000003086 colorant Substances 0.000 description 9
- 239000004925 Acrylic resin Substances 0.000 description 8
- 229920000178 Acrylic resin Polymers 0.000 description 8
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 8
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 8
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 6
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- 239000002998 adhesive polymer Substances 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 4
- 229920001519 homopolymer Polymers 0.000 description 4
- 239000004014 plasticizer Substances 0.000 description 4
- 238000006116 polymerization reaction Methods 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 3
- 239000004593 Epoxy Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000011259 mixed solution Substances 0.000 description 3
- 238000007639 printing Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 238000010345 tape casting Methods 0.000 description 3
- 125000001302 tertiary amino group Chemical group 0.000 description 3
- 238000002834 transmittance Methods 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- NQUXRXBRYDZZDL-UHFFFAOYSA-N 1-(2-prop-2-enoyloxyethyl)cyclohexane-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCCCC1(CCOC(=O)C=C)C(O)=O NQUXRXBRYDZZDL-UHFFFAOYSA-N 0.000 description 2
- 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 2
- IEQWWMKDFZUMMU-UHFFFAOYSA-N 2-(2-prop-2-enoyloxyethyl)butanedioic acid Chemical compound OC(=O)CC(C(O)=O)CCOC(=O)C=C IEQWWMKDFZUMMU-UHFFFAOYSA-N 0.000 description 2
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 2
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 description 2
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 2
- CYUZOYPRAQASLN-UHFFFAOYSA-N 3-prop-2-enoyloxypropanoic acid Chemical compound OC(=O)CCOC(=O)C=C CYUZOYPRAQASLN-UHFFFAOYSA-N 0.000 description 2
- SXIFAEWFOJETOA-UHFFFAOYSA-N 4-hydroxy-butyl Chemical group [CH2]CCCO SXIFAEWFOJETOA-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- PQJYXFVJBSRUPG-UHFFFAOYSA-N [3-(2-methylaziridine-1-carbonyl)phenyl]-(2-methylaziridin-1-yl)methanone Chemical compound CC1CN1C(=O)C1=CC=CC(C(=O)N2C(C2)C)=C1 PQJYXFVJBSRUPG-UHFFFAOYSA-N 0.000 description 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005227 gel permeation chromatography Methods 0.000 description 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N isopropyl alcohol Natural products CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 2
- 125000005359 phenoxyalkyl group Chemical group 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920006267 polyester film Polymers 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 239000001054 red pigment Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- NOBYOEQUFMGXBP-UHFFFAOYSA-N (4-tert-butylcyclohexyl) (4-tert-butylcyclohexyl)oxycarbonyloxy carbonate Chemical compound C1CC(C(C)(C)C)CCC1OC(=O)OOC(=O)OC1CCC(C(C)(C)C)CC1 NOBYOEQUFMGXBP-UHFFFAOYSA-N 0.000 description 1
- KCZQSKKNAGZQSZ-UHFFFAOYSA-N 1,3,5-tris(6-isocyanatohexyl)-1,3,5-triazin-2,4,6-trione Chemical compound O=C=NCCCCCCN1C(=O)N(CCCCCCN=C=O)C(=O)N(CCCCCCN=C=O)C1=O KCZQSKKNAGZQSZ-UHFFFAOYSA-N 0.000 description 1
- OSSNTDFYBPYIEC-UHFFFAOYSA-N 1-ethenylimidazole Chemical compound C=CN1C=CN=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-N 0.000 description 1
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- DPBJAVGHACCNRL-UHFFFAOYSA-N 2-(dimethylamino)ethyl prop-2-enoate Chemical compound CN(C)CCOC(=O)C=C DPBJAVGHACCNRL-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- PLWQJHWLGRXAMP-UHFFFAOYSA-N 2-ethenoxy-n,n-diethylethanamine Chemical compound CCN(CC)CCOC=C PLWQJHWLGRXAMP-UHFFFAOYSA-N 0.000 description 1
- JWCDUUFOAZFFMX-UHFFFAOYSA-N 2-ethenoxy-n,n-dimethylethanamine Chemical compound CN(C)CCOC=C JWCDUUFOAZFFMX-UHFFFAOYSA-N 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- JNDVNJWCRZQGFQ-UHFFFAOYSA-N 2-methyl-N,N-bis(methylamino)hex-2-enamide Chemical compound CCCC=C(C)C(=O)N(NC)NC JNDVNJWCRZQGFQ-UHFFFAOYSA-N 0.000 description 1
- RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 description 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 1
- QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 description 1
- VFXXTYGQYWRHJP-UHFFFAOYSA-N 4,4'-azobis(4-cyanopentanoic acid) Chemical compound OC(=O)CCC(C)(C#N)N=NC(C)(CCC(O)=O)C#N VFXXTYGQYWRHJP-UHFFFAOYSA-N 0.000 description 1
- XSLWOAFWQUGVDC-UHFFFAOYSA-N 4-(4-chlorophenyl)-3-hydroxy-1-phenyl-2H-pyrrolo[3,4-c]pyrrol-6-one Chemical compound Oc1[nH]c(c2C(=O)N=C(c12)c1ccc(Cl)cc1)-c1ccccc1 XSLWOAFWQUGVDC-UHFFFAOYSA-N 0.000 description 1
- CBZMQWPBAUBAPO-UHFFFAOYSA-N 4-ethenyl-n,n-diethylaniline Chemical compound CCN(CC)C1=CC=C(C=C)C=C1 CBZMQWPBAUBAPO-UHFFFAOYSA-N 0.000 description 1
- GQWAOUOHRMHSHL-UHFFFAOYSA-N 4-ethenyl-n,n-dimethylaniline Chemical compound CN(C)C1=CC=C(C=C)C=C1 GQWAOUOHRMHSHL-UHFFFAOYSA-N 0.000 description 1
- DXPPIEDUBFUSEZ-UHFFFAOYSA-N 6-methylheptyl prop-2-enoate Chemical compound CC(C)CCCCCOC(=O)C=C DXPPIEDUBFUSEZ-UHFFFAOYSA-N 0.000 description 1
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 1
- 229920001944 Plastisol Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 150000003926 acrylamides Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000007869 azo polymerization initiator Substances 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- 150000001718 carbodiimides Chemical class 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 150000004292 cyclic ethers Chemical group 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 238000009408 flooring Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 125000005641 methacryl group Chemical group 0.000 description 1
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- DFENKTCEEGOWLB-UHFFFAOYSA-N n,n-bis(methylamino)-2-methylidenepentanamide Chemical compound CCCC(=C)C(=O)N(NC)NC DFENKTCEEGOWLB-UHFFFAOYSA-N 0.000 description 1
- FTQWRYSLUYAIRQ-UHFFFAOYSA-N n-[(octadecanoylamino)methyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCNC(=O)CCCCCCCCCCCCCCCCC FTQWRYSLUYAIRQ-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N o-dicarboxybenzene Natural products OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920006287 phenoxy resin Polymers 0.000 description 1
- 239000013034 phenoxy resin Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 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
- STIABRLGDKHASC-UHFFFAOYSA-N phthalic acid;prop-2-enoic acid Chemical compound OC(=O)C=C.OC(=O)C1=CC=CC=C1C(O)=O STIABRLGDKHASC-UHFFFAOYSA-N 0.000 description 1
- 239000004999 plastisol Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/14—Homopolymers or copolymers of esters of esters containing halogen, nitrogen, sulfur, or oxygen atoms in addition to the carboxy oxygen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2333/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers
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Description
本発明の(メタ)アクリル系フィルムは、カルボキシル基含有(メタ)アクリル系ポリマーと、アミノ基含有(メタ)アクリル系ポリマーと、ポリアクリレートと、架橋剤とを含んでいる。本明細書において「(メタ)アクリル」とは、アクリル又はメタクリルを意味する。
本明細書で開示された(メタ)アクリル系フィルムを用いたマーキングフィルム(200)の一例について、図3に沿って説明する。
本明細書においては、以下の略称を使用することがある。
MA :メチルアクリレート
MMA :メチルメタクリレート
BA :ブチルアクリレ−ト
BMA :ブチルメタアクリレート
iBMA :イソブチルメタアクリレート
IOA :イソオクチルアクリレート
DEMAEMA:ジメチルアミノエチルメタクリレート
AA :アクリル酸
MAA :メチルメタクリル酸
HEA :ヒドロキシエチルアクリレート
((メタ)アクリル系ポリマーの製造)
本実施例、比較例で使用する(メタ)アクリル系ポリマーを以下の手順で作製した。
本明細書に示すポリマーのガラス転移点は特に記載がある場合を除き、各ポリマーがn種類のモノマーから共重合されているとして、FOXの式(下式)より求めた値である。
1/Tg=X1/(Tg1+273.15)+X2/(Tg2+273.15)+・・・+Xn/(Tgn+273.15)
Tg1:成分1のホモポリマーのガラス転移点
Tg2:成分2のホモポリマーのガラス転移点
X1:重合の際に添加した成分1のモノマーの重量分率
X2:重合の際に添加した成分2のモノマーの重量分率
X1+X2+・・・+Xn=1
本明細書に示すポリマーの重量平均分子量は特に記載がある場合を除き、ゲルパーミエーションクロマトグラフィー(GPC)法によるスチレン換算分子量を意味する。
本実施例、比較例では以下のポリアクリレートを使用した。なお、本明細書では、直鎖型とはOH基やカルボキシル基といった官能基が分子鎖末端にのみ存在するポリアクリレートをいい、分岐型とは側鎖に官能基が含まれるポリアクリレートをいう。
ポリアクリレート2:綜研化学社製 商品名「アクトフローUMB2005」、OH基含有分岐型 BA主モノマー共重合体、重量平均分子量(Mw)は2,200、Tgは−54℃
ポリアクリレート3:綜研化学社製 商品名「アクトフローCBB3098」、カルボキシル基含有分岐型 BA主モノマー共重合体、重量平均分子量(Mw)は3,000、Tgは−44℃
アクリルポリオール樹脂(住友バイエルウレタン(株)社製 商品名「デスモフェンA365」)と、HDIイソシアヌレート(住友バイエルウレタン(株)社製 商品名「スミジュールN3300」)とを、イソシアネート基と水酸基を当量比1.0([NCO]/[OH]当量比=1.0)となるように混合し保護層用樹脂溶液を作製した。50μm厚さの剥離処理されたポリエステルフィルムにこの樹脂溶液をナイフコートで塗布し、85℃で5分乾燥することで、厚さ3μmの保護層を作製した。
(メタ)アクリル系フィルム用樹脂溶液の配合比、種類を、表1に記載したものに変更した以外は実施例1と同様にして(メタ)アクリル系フィルム、およびマーキングフィルムを得た。
表1に記載された配合比の(メタ)アクリル系フィルム用樹脂溶液を準備し、これにポリマー3が100質量部に対して1.25質量部になるようにエポキシ系架橋剤(綜研化学社製 商品名「E−AX」)を添加した。この溶液をナイフコートにより、50μm厚さの剥離処理されたポリエステルフィルムに塗布し、90℃で10分乾燥することで乾燥後の厚さが50μmとなる(メタ)アクリル系フィルムを得た。実施例1と同様にして接着剤層を作製した後、この接着剤層を前記(メタ)アクリル系フィルムにドライラミネートをしてマーキングフィルムを得た。
被着体として、図4に記載された形状のアルミニウム製のコルゲート板(山の高さ(H):5mm、山の幅(W):20mm、山のピッチ(P):45mm)を用意した。マーキングフィルムを長さ100mm×幅50mmに切断した試験片を5℃環境下で24時間養生した後、スキージーにてコルゲート板の凹凸部へ押し込み貼り付けた。凹凸部への押し込みの際に破断が生じない場合を“Good”と、押し込み時の破断が生じる場合を“Poor”と評価した。
マーキングフィルムの引張弾性率を、JISK7127(1989)に規定される方法に準拠し、以下の条件で測定した。
測定温度:20℃
試験片形状:1号型(幅25mm)
引張速度:300mm/min
低温下での追従性試験の後、さらに貼り付けた試験片を端部から剥離し外観を確認した。剥離の際に試験片に亀裂が入らない場合は、“Good”と、剥離時の亀裂が生じる場合は“Poor”と評価した。
長さ150mm×幅70mm×厚さ1mmのアルミニウム板に、長さ150mm×幅70mmの試験片を貼り付け20℃環境下にて24時間養生した。その後、ASTM D5420−04に準拠してガードナーインパクト試験機を用いて、試験片貼り付け面の裏側より衝撃を与えて評価した。1ポンドの重りを落とす距離を次第に高くしていき、試験後、試験片の表面に亀裂や破裂が確認されない点を耐衝撃性値とした。耐衝撃性値の単位としては、高さ(インチ)×重さ(ポンド)をmm・kgに換算したものを用いた。
(メタ)アクリル系フィルム用樹脂溶液を、ホモミキサー(特殊機械工業株式会社製 「T.K.AUTO HOMOMIXER」)にて回転数900rpmで10分攪拌し、30分放置後溶液外観を目視にて観察した。各成分が相溶し溶液が透明であった場合は“Good”、透明でなかった場合は“Poor”とした。
2 第2の(メタ)アクリル系フィルム層
3 着色剤
4 保護層
5 レセプター層
6 接着剤層
Claims (8)
- カルボキシル基含有(メタ)アクリル系ポリマーと、アミノ基含有(メタ)アクリル系ポリマーと、反応性官能基を含み重量平均分子量が1000から4000の範囲のポリアクリレートと、アミノ基またはカルボキシル基と反応する官能基を有する架橋剤とを含んでいる(メタ)アクリル系フィルムであって、
前記カルボキシル基含有(メタ)アクリル系ポリマーと前記アミノ基含有(メタ)アクリル系ポリマーとの総量100質量部に対して、前記ポリアクリレートを0.5から30質量部の範囲で含んでおり、
前記反応性官能基が水酸基である(メタ)アクリル系フィルム。 - カルボキシル基含有(メタ)アクリル系ポリマーと、アミノ基含有(メタ)アクリル系ポリマーと、反応性官能基を含み重量平均分子量が1000から4000の範囲のポリアクリレートと、アミノ基またはカルボキシル基と反応する官能基を有する架橋剤とを含んでいる(メタ)アクリル系フィルムであって、
前記カルボキシル基含有(メタ)アクリル系ポリマーと前記アミノ基含有(メタ)アクリル系ポリマーとの総量100質量部に対して、前記ポリアクリレートを0.5から30質量部の範囲で含んでおり、
前記ポリアクリレートが分子鎖末端にのみ官能基を有する(メタ)アクリル系フィルム。 - 前記ポリアクリレートの結合アルキル基(R)の炭素数が、前記カルボキシル基含有(メタ)アクリル系ポリマーまたは前記アミノ基含有(メタ)アクリル系ポリマーのいずれかの結合アルキル基(R)の炭素数と同じである請求項1または請求項2に記載の(メタ)アクリル系フィルム。
- 顔料または染料が分散されている請求項1から請求項3のいずれか一項に記載の(メタ)アクリル系フィルム。
- 第1主要面と第2主要面とを備える請求項1から請求項4のいずれか一項に記載の(メタ)アクリル系フィルムであって、該第1主要面側に保護層を有する(メタ)アクリル系フィルム。
- 前記カルボキシル基含有(メタ)アクリル系ポリマーのガラス転移点が0℃以上であり、前記アミノ基含有(メタ)アクリル系ポリマーのガラス転移点が0℃以下である請求項1から請求項5のいずれか一項に記載の(メタ)アクリル系フィルム。
- 前記カルボキシル基含有(メタ)アクリル系ポリマーのガラス転移点が0℃以下であり、前記アミノ基含有(メタ)アクリル系ポリマーのガラス転移点が0℃以上である請求項1から請求項5のいずれか一項に記載の(メタ)アクリル系フィルム。
- 第1主要面と第2主要面とを備える請求項1から請求項7のいずれか一項に記載の(メタ)アクリル系フィルムと、該第2主要面側に配置された接着剤層とを有するマーキングフィルム。
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EP08840940A EP2205664B1 (en) | 2007-10-26 | 2008-10-21 | (meth)acrylic film and marking film using same |
CN2008801130698A CN101835826B (zh) | 2007-10-26 | 2008-10-21 | (甲基)丙烯酸类薄膜和采用该薄膜的标记膜 |
US12/739,468 US20100323195A1 (en) | 2007-10-26 | 2008-10-21 | (meth)acrylic film and marking film using same |
PL08840940T PL2205664T3 (pl) | 2007-10-26 | 2008-10-21 | Folia (met)akrylowa i folia znacznikowa |
AT08840940T ATE541881T1 (de) | 2007-10-26 | 2008-10-21 | (meth)acrylfolie und markierungsfolie unter verwendung davon |
PCT/US2008/080628 WO2009055378A2 (en) | 2007-10-26 | 2008-10-21 | (meth)acrylic film and marking film using same |
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JP5085870B2 (ja) * | 2006-02-10 | 2012-11-28 | スリーエム イノベイティブ プロパティズ カンパニー | 画像受容性材料及び画像受容シート |
-
2007
- 2007-10-26 JP JP2007279299A patent/JP5307378B2/ja active Active
-
2008
- 2008-10-21 WO PCT/US2008/080628 patent/WO2009055378A2/en active Application Filing
- 2008-10-21 EP EP08840940A patent/EP2205664B1/en not_active Not-in-force
- 2008-10-21 PL PL08840940T patent/PL2205664T3/pl unknown
- 2008-10-21 AT AT08840940T patent/ATE541881T1/de active
- 2008-10-21 CN CN2008801130698A patent/CN101835826B/zh active Active
- 2008-10-21 US US12/739,468 patent/US20100323195A1/en not_active Abandoned
- 2008-10-24 TW TW097141112A patent/TW200936651A/zh unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR102645990B1 (ko) * | 2020-08-11 | 2024-03-08 | 후지모리 고교 가부시키가이샤 | (메타)아크릴계 수지 조성물 및 (메타)아크릴계 수지 필름 |
Also Published As
Publication number | Publication date |
---|---|
ATE541881T1 (de) | 2012-02-15 |
CN101835826A (zh) | 2010-09-15 |
PL2205664T3 (pl) | 2012-06-29 |
CN101835826B (zh) | 2013-11-27 |
WO2009055378A2 (en) | 2009-04-30 |
JP2009108136A (ja) | 2009-05-21 |
TW200936651A (en) | 2009-09-01 |
US20100323195A1 (en) | 2010-12-23 |
EP2205664B1 (en) | 2012-01-18 |
EP2205664A4 (en) | 2010-11-03 |
WO2009055378A3 (en) | 2009-08-06 |
EP2205664A2 (en) | 2010-07-14 |
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