JP2008095044A - Resin composition for sealing material - Google Patents
Resin composition for sealing material Download PDFInfo
- Publication number
- JP2008095044A JP2008095044A JP2006281589A JP2006281589A JP2008095044A JP 2008095044 A JP2008095044 A JP 2008095044A JP 2006281589 A JP2006281589 A JP 2006281589A JP 2006281589 A JP2006281589 A JP 2006281589A JP 2008095044 A JP2008095044 A JP 2008095044A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- mass
- ethylene
- heat
- resin composition
- 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.)
- Granted
Links
- 239000011342 resin composition Substances 0.000 title claims abstract description 43
- 239000003566 sealing material Substances 0.000 title description 8
- 229920005989 resin Polymers 0.000 claims abstract description 51
- 239000011347 resin Substances 0.000 claims abstract description 51
- 229920006026 co-polymeric resin Polymers 0.000 claims abstract description 41
- 238000007789 sealing Methods 0.000 claims abstract description 21
- 239000004793 Polystyrene Substances 0.000 claims abstract description 18
- 229920002223 polystyrene Polymers 0.000 claims abstract description 18
- 229920001567 vinyl ester resin Polymers 0.000 claims abstract description 18
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 54
- 239000005977 Ethylene Substances 0.000 claims description 54
- 238000000034 method Methods 0.000 claims description 17
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 15
- 239000003208 petroleum Substances 0.000 claims description 11
- 238000006116 polymerization reaction Methods 0.000 claims description 11
- 229920003067 (meth)acrylic acid ester copolymer Polymers 0.000 claims description 8
- 229920001038 ethylene copolymer Polymers 0.000 claims description 8
- 239000000155 melt Substances 0.000 claims description 5
- 150000002148 esters Chemical class 0.000 claims description 4
- 239000000463 material Substances 0.000 abstract description 26
- 229920003023 plastic Polymers 0.000 abstract description 11
- 239000004033 plastic Substances 0.000 abstract description 11
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 abstract description 7
- 239000012775 heat-sealing material Substances 0.000 abstract description 7
- 235000013305 food Nutrition 0.000 abstract description 5
- 230000000704 physical effect Effects 0.000 abstract description 4
- 230000002633 protecting effect Effects 0.000 abstract 1
- 239000000203 mixture Substances 0.000 description 23
- 229920001577 copolymer Polymers 0.000 description 18
- -1 polyethylene Polymers 0.000 description 18
- 238000002156 mixing Methods 0.000 description 15
- 239000004698 Polyethylene Substances 0.000 description 11
- 229920000573 polyethylene Polymers 0.000 description 11
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 8
- 239000000654 additive Substances 0.000 description 7
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- UAUDZVJPLUQNMU-KTKRTIGZSA-N erucamide Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(N)=O UAUDZVJPLUQNMU-KTKRTIGZSA-N 0.000 description 6
- 230000000379 polymerizing effect Effects 0.000 description 6
- 239000013032 Hydrocarbon resin Substances 0.000 description 5
- 239000004794 expanded polystyrene Substances 0.000 description 5
- 229920006270 hydrocarbon resin Polymers 0.000 description 5
- 239000010410 layer Substances 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- GRWFGVWFFZKLTI-IUCAKERBSA-N (-)-α-pinene Chemical compound CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 description 4
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 4
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 4
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- 239000004743 Polypropylene Substances 0.000 description 4
- 229910021536 Zeolite Inorganic materials 0.000 description 4
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 229920000728 polyester Polymers 0.000 description 4
- 229920001155 polypropylene Polymers 0.000 description 4
- 239000010457 zeolite Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 125000002723 alicyclic group Chemical group 0.000 description 3
- 229920006271 aliphatic hydrocarbon resin Polymers 0.000 description 3
- 229920006272 aromatic hydrocarbon resin Polymers 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 229920006248 expandable polystyrene Polymers 0.000 description 3
- 229920005669 high impact polystyrene Polymers 0.000 description 3
- 235000012149 noodles Nutrition 0.000 description 3
- LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 238000010526 radical polymerization reaction Methods 0.000 description 3
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 2
- MVNCAPSFBDBCGF-UHFFFAOYSA-N alpha-pinene Natural products CC1=CCC23C1CC2C3(C)C MVNCAPSFBDBCGF-UHFFFAOYSA-N 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 235000013527 bean curd Nutrition 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 2
- 150000001993 dienes Chemical group 0.000 description 2
- 238000006471 dimerization reaction Methods 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000011953 free-radical catalyst Substances 0.000 description 2
- 239000004797 high-impact polystyrene Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
- 235000015110 jellies Nutrition 0.000 description 2
- 239000008274 jelly Substances 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 150000003097 polyterpenes Chemical class 0.000 description 2
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 2
- 235000011962 puddings Nutrition 0.000 description 2
- GRWFGVWFFZKLTI-UHFFFAOYSA-N rac-alpha-Pinene Natural products CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 description 2
- 230000003578 releasing effect Effects 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 238000005979 thermal decomposition reaction Methods 0.000 description 2
- 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 2
- 235000013618 yogurt Nutrition 0.000 description 2
- 239000004711 α-olefin Substances 0.000 description 2
- WTARULDDTDQWMU-RKDXNWHRSA-N (+)-β-pinene Chemical compound C1[C@H]2C(C)(C)[C@@H]1CCC2=C WTARULDDTDQWMU-RKDXNWHRSA-N 0.000 description 1
- WTARULDDTDQWMU-IUCAKERBSA-N (-)-Nopinene Natural products C1[C@@H]2C(C)(C)[C@H]1CCC2=C WTARULDDTDQWMU-IUCAKERBSA-N 0.000 description 1
- OYUBNQOGHWGLJB-WRBBJXAJSA-N (13z,33z)-hexatetraconta-13,33-dienediamide Chemical compound NC(=O)CCCCCCCCCCC\C=C/CCCCCCCCCCCCCCCCCC\C=C/CCCCCCCCCCCC(N)=O OYUBNQOGHWGLJB-WRBBJXAJSA-N 0.000 description 1
- PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical compound C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-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
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-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
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 description 1
- TZCGFWIYMJNJIO-UHFFFAOYSA-N 4-methylpentyl 2-methylprop-2-enoate Chemical compound CC(C)CCCOC(=O)C(C)=C TZCGFWIYMJNJIO-UHFFFAOYSA-N 0.000 description 1
- BDMYQVMQTKUZNB-UHFFFAOYSA-N 4-methylpentyl prop-2-enoate Chemical compound CC(C)CCCOC(=O)C=C BDMYQVMQTKUZNB-UHFFFAOYSA-N 0.000 description 1
- NQSLZEHVGKWKAY-UHFFFAOYSA-N 6-methylheptyl 2-methylprop-2-enoate Chemical compound CC(C)CCCCCOC(=O)C(C)=C NQSLZEHVGKWKAY-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
- 229920002126 Acrylic acid copolymer Polymers 0.000 description 1
- KJBQXFIRXNDPLN-AUYXYSRISA-N CCCCCCCC/C=C\CCCCCCCCNCCCCCCCC/C=C\CCCCCCCC=C Chemical compound CCCCCCCC/C=C\CCCCCCCCNCCCCCCCC/C=C\CCCCCCCC=C KJBQXFIRXNDPLN-AUYXYSRISA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- ORAWFNKFUWGRJG-UHFFFAOYSA-N Docosanamide Chemical compound CCCCCCCCCCCCCCCCCCCCCC(N)=O ORAWFNKFUWGRJG-UHFFFAOYSA-N 0.000 description 1
- UAUDZVJPLUQNMU-UHFFFAOYSA-N Erucasaeureamid Natural products CCCCCCCCC=CCCCCCCCCCCCC(N)=O UAUDZVJPLUQNMU-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Natural products OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- WTARULDDTDQWMU-UHFFFAOYSA-N Pseudopinene Natural products C1C2C(C)(C)C1CCC2=C WTARULDDTDQWMU-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000004840 adhesive resin Substances 0.000 description 1
- 229920006223 adhesive resin Polymers 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- XCPQUQHBVVXMRQ-UHFFFAOYSA-N alpha-Fenchene Natural products C1CC2C(=C)CC1C2(C)C XCPQUQHBVVXMRQ-UHFFFAOYSA-N 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
- 229930006722 beta-pinene Natural products 0.000 description 1
- 235000013361 beverage Nutrition 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical class C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 150000001728 carbonyl compounds Chemical class 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
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- 125000004122 cyclic group Chemical group 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000007323 disproportionation reaction Methods 0.000 description 1
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- 229940079593 drug Drugs 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
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- 239000001530 fumaric acid Substances 0.000 description 1
- LCWMKIHBLJLORW-UHFFFAOYSA-N gamma-carene Natural products C1CC(=C)CC2C(C)(C)C21 LCWMKIHBLJLORW-UHFFFAOYSA-N 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- HSEMFIZWXHQJAE-UHFFFAOYSA-N hexadecanamide Chemical compound CCCCCCCCCCCCCCCC(N)=O HSEMFIZWXHQJAE-UHFFFAOYSA-N 0.000 description 1
- LNCPIMCVTKXXOY-UHFFFAOYSA-N hexyl 2-methylprop-2-enoate Chemical compound CCCCCCOC(=O)C(C)=C LNCPIMCVTKXXOY-UHFFFAOYSA-N 0.000 description 1
- LNMQRPPRQDGUDR-UHFFFAOYSA-N hexyl prop-2-enoate Chemical compound CCCCCCOC(=O)C=C LNMQRPPRQDGUDR-UHFFFAOYSA-N 0.000 description 1
- 235000012907 honey Nutrition 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 150000002432 hydroperoxides Chemical class 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 239000001282 iso-butane Substances 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
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- 238000003475 lamination Methods 0.000 description 1
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- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
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- 150000005673 monoalkenes Chemical group 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- NWZZFAQUBMRYNU-UHFFFAOYSA-N n-octadecylnonadec-18-en-1-amine Chemical compound CCCCCCCCCCCCCCCCCCNCCCCCCCCCCCCCCCCCC=C NWZZFAQUBMRYNU-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- NZIDBRBFGPQCRY-UHFFFAOYSA-N octyl 2-methylprop-2-enoate Chemical compound CCCCCCCCOC(=O)C(C)=C NZIDBRBFGPQCRY-UHFFFAOYSA-N 0.000 description 1
- ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 description 1
- FATBGEAMYMYZAF-KTKRTIGZSA-N oleamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(N)=O FATBGEAMYMYZAF-KTKRTIGZSA-N 0.000 description 1
- 125000001117 oleyl 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])=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
- 238000005457 optimization Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
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Abstract
Description
本発明は、シール材用樹脂組成物に関し、より詳細には、エチレン・ビニルエステル共重合体樹脂とエチレン・(メタ)アクリル酸エステル共重合体樹脂及び粘着性付与樹脂との特定配合量比の樹脂組成物からなり、プラスチック容器、特に、耐衝撃性ポリスチレン製容器と蓋体とのシールに好適に用いられるシール材用樹脂組成物に関する。 The present invention relates to a resin composition for a sealing material, and more specifically, a specific blending ratio of an ethylene / vinyl ester copolymer resin, an ethylene / (meth) acrylate copolymer resin and a tackifier resin. The present invention relates to a resin composition for a sealing material, which is made of a resin composition and is suitably used for sealing a plastic container, in particular, an impact-resistant polystyrene container and a lid.
ゼリー、プリン、ヨーグルト、豆腐、即席メン、ヌードル類など各種の食品類や医薬品容器として、易開封性蓋を備えたプラスチック容器が広く使用されている。
特に、カップ入り即席メン、ヌードル、汁粉などの容器素材には発泡ポリスチレンシート又はこれに耐衝撃性ポリスチレンフィルムを貼り合わせたもの、耐衝撃性ポリスチレンシート、ポリエチレンラミネート紙などを素材とする容器が広く用いられている。
そしてこれらプラスチック容器を蓋体で易開封状に密封シールするためのヒートシール材として従来から種々のものが提案、実用化されているが、中でも、エチレン・酢酸ビニル共重合体と粘着性付与樹脂との組成物、これにポリエチレンや低結晶性エチレン・α−オレフィン共重合体などを配合した組成物は、容器本体と蓋体との密封性が比較的良好で、且つ、蓋体剥離時の剥離強度が概ね妥当なことから広く使用されている。
Plastic containers with easy-open lids are widely used as various foods and pharmaceutical containers such as jelly, pudding, yogurt, tofu, instant men and noodles.
In particular, container materials such as instant men in cups, noodles, and soup powders are widely made of foamed polystyrene sheets or those with impact-resistant polystyrene films bonded to them, impact-resistant polystyrene sheets, polyethylene laminated paper, etc. It is used.
Various heat sealing materials have been proposed and put to practical use for sealing and sealing these plastic containers in an easy-open form with lids. Among them, ethylene / vinyl acetate copolymers and tackifying resins are among others. And a composition in which polyethylene or a low crystalline ethylene / α-olefin copolymer is blended with this, the sealing performance between the container body and the lid is relatively good, and when the lid is peeled off. Widely used because peel strength is generally reasonable.
例えば、特許文献1には、エチレン・酢酸ビニル共重合体とポリエチレンと粘着性付与剤の特定配合量比の樹脂組成物からなり、発泡ポリスチレンや耐衝撃性ポリスチレン製容器と蓋材とのヒートシーラントに用いられる接着性組成物の発明が開示されている。 For example, Patent Document 1 includes a resin composition having a specific blending ratio of an ethylene / vinyl acetate copolymer, polyethylene, and a tackifier, and a heat sealant of a foamed polystyrene or impact polystyrene container and a lid. The invention of the adhesive composition used in the present invention is disclosed.
又、特許文献2には、エチレン・不飽和エステル共重合体と水素添加スチレン・ブタジエン共重合体とを必須成分としてなる耐衝撃性ポリスチレン容器と蓋体とのヒートシールに用いられる樹脂組成物の発明が開示されている。 Patent Document 2 discloses a resin composition used for heat-sealing an impact-resistant polystyrene container and a lid body, each comprising an ethylene / unsaturated ester copolymer and a hydrogenated styrene / butadiene copolymer as essential components. The invention is disclosed.
しかしながら、最近では、上記容器と蓋との易開封性の最適化、特にシール剥離時の剥離強度が適正で、低温でも適正強度でのスムーズな剥離が達成されることが強く求められている。
又、用途によっては、容器本体や蓋材のコート層等に用いられる材質の関係等からヒートシールを通常よりやや低い温度、例えば、120℃近傍の温度で実施することが求められる等、望まれるヒートシール特性が異なっていたり、他の特性が要求されたりすることがあり、このような要求にも耐えられるようなシール材が望まれている。
However, recently, there has been a strong demand for optimization of easy opening between the container and the lid, particularly when the peel strength at the time of seal peeling is appropriate, and smooth peeling at an appropriate strength can be achieved even at low temperatures.
In addition, depending on the application, it is desirable that heat sealing be performed at a temperature slightly lower than usual, for example, a temperature around 120 ° C., due to the relationship of materials used for the container body and the coating layer of the lid material, etc. The heat seal characteristics may be different or other characteristics may be required, and a sealing material that can withstand such requirements is desired.
又、上記剥離を途中で止める部分剥離が好適に遂行できるために、剥離時にスムースで良好な剥離感を与えることも要求されるが、従来、既存のシール材を用いると、あるものは低温で良好なシール処理が出来なかったり、あるものはシール強度が小さかったり、あるものは初期シール強度として充分な値を示すが経時的にシール強度が低下するといった欠点を示し、実使用にはそれぞれ何らかの問題を包含し、上記要件を完全に満たすシール材を選択することは可成り困難であった。
本発明者等は、上記要件を完全に充足するシール材を開発することを目指して鋭意研究を重ねた結果、エチレン・酢酸ビニル共重合体樹脂等のエチレン・ビニルエステル共重合体樹脂とエチレン・(メタ)アクリル酸エステルと粘着性付与樹脂との特定配合量比からなる樹脂組成物が上記要件を充足出来ることを見出し、この知見に基づき本発明を完成するに至った。 As a result of intensive research aimed at developing a sealing material that completely satisfies the above requirements, the present inventors have found that ethylene / vinyl ester copolymer resins such as ethylene / vinyl acetate copolymer resins and ethylene It discovered that the resin composition which consists of a specific compounding quantity ratio of (meth) acrylic acid ester and tackifying resin can satisfy the said requirements, and came to complete this invention based on this knowledge.
従って、本発明の目的は、発泡ポリスチレンや耐衝撃性ポリスチレン等のプラスチック材に対するヒートシール性に優れ、特に、従来品より低温でヒートシールを実施してもシール性に顕著に優れるヒートシール材用樹脂組成物を提供するにある。
又、本発明は、従来品ヒートシール材に比べて耐熱性に優れ、且つ、発泡ポリスチレンや耐衝撃性ポリスチレン等のプラスチック材に対し適度な剥離強度とスムーズで快い剥離感触を有し、プラスチック容器と易開封性蓋との間のヒートシール材として好適なヒートシール材用樹脂組成物を提供することを目的とする。
Therefore, the object of the present invention is excellent in heat sealability for plastic materials such as expanded polystyrene and impact-resistant polystyrene, and particularly for heat seal materials that are remarkably excellent in sealability even when heat sealing is performed at a lower temperature than conventional products. It is in providing a resin composition.
In addition, the present invention is superior in heat resistance compared to conventional heat seal materials, and has an appropriate peel strength and a smooth and pleasant peel feel against plastic materials such as expanded polystyrene and impact-resistant polystyrene. It aims at providing the resin composition for heat seal materials suitable as a heat seal material between an easily openable lid.
本発明によれば、エチレン・ビニルエステル共重合体樹脂(A)30〜80質量部、エチレン・(メタ)アクリル酸エステル共重合体樹脂(B)1〜45質量部及び粘着性付与樹脂(C)3〜30質量部(但し(A)、(B)、(C)樹脂の合計量は100質量部)を含んでなるシール材用樹脂組成物が提供される。
なお本発明において(メタ)アクリル酸エステルとはメタクリル酸エステルあるいはアクリル酸エステルを意味する。
According to the present invention, 30 to 80 parts by mass of an ethylene / vinyl ester copolymer resin (A), 1 to 45 parts by mass of an ethylene / (meth) acrylate copolymer resin (B) and a tackifier resin (C ) 3 to 30 parts by mass (provided that the total amount of the resins (A), (B), and (C) is 100 parts by mass) is provided.
In the present invention, (meth) acrylic acid ester means methacrylic acid ester or acrylic acid ester.
本発明のヒートシール性樹脂組成物は、エチレン・酢酸ビニル共重合体樹脂等のエチレン・ビニルエステル共重合体樹脂とエチレン・(メタ)アクリル酸エステル共重合体樹脂と粘着性付与樹脂とを特定量比で配合して得られた樹脂組成物である点を構成上の特徴とする。
上記組成物は、類似の従来品ヒートシール材に比較して低温でのヒートシール処理が可能であるにもかかわらず、耐熱性に優れ、且つ、特に発泡ポリスチレンや耐衝撃性ポリスチレン等に対し適度な剥離強度とスムーズで快い剥離感触を有する。
The heat-sealable resin composition of the present invention specifies an ethylene / vinyl ester copolymer resin such as an ethylene / vinyl acetate copolymer resin, an ethylene / (meth) acrylate copolymer resin, and a tackifier resin. The point which is the resin composition obtained by mix | blending with a quantitative ratio makes it the characteristic on a structure.
The above composition is excellent in heat resistance, although it can be heat-sealed at a low temperature compared to similar conventional heat-sealing materials, and is particularly suitable for expanded polystyrene, impact-resistant polystyrene, etc. Excellent peel strength and smooth and pleasant peel feeling.
本発明の上記樹脂組成物は、 190℃、2160g荷重におけるメルトフローレート(MFR)(JIS K7210−1999に準拠して測定)が0.1〜100g/10分であることが好ましい。
又、前記エチレン・ビニルエステル共重合体樹脂(A)が酢酸ビニル成分単位含有率5〜30質量%のエチレン・酢酸ビニル共重合体樹脂であることが好ましい。
又、前記エチレン・(メタ)アクリル酸エステル共重合体樹脂(B)のエステル成分単位の含有率が2〜48質量%であるものが好ましく、その内でも、チューブラー高圧重合法により得られたものが特に好ましい。
又、前記粘着性樹脂(C)は水素添加石油樹脂であることが好ましい。
更に、本発明の樹脂組成物は、耐衝撃性ポリスチレン製容器のヒートシールに特に好適に用いられる。
The resin composition of the present invention preferably has a melt flow rate (MFR) at 190 ° C. under a load of 2160 g (measured according to JIS K7210-1999) of 0.1 to 100 g / 10 min.
The ethylene / vinyl ester copolymer resin (A) is preferably an ethylene / vinyl acetate copolymer resin having a vinyl acetate component unit content of 5 to 30% by mass.
The ethylene / (meth) acrylic acid ester copolymer resin (B) preferably has an ester component unit content of 2 to 48% by mass, and among them, it was obtained by a tubular high pressure polymerization method. Those are particularly preferred.
The adhesive resin (C) is preferably a hydrogenated petroleum resin.
Furthermore, the resin composition of the present invention is particularly preferably used for heat sealing of impact-resistant polystyrene containers.
本発明のヒートシール材用樹脂組成物は、上記特定構成により、プラスチック製容器、特に、耐衝撃性ポリスチレン、発泡ポリスチレン等の素材プラスチックからなる容器に用いるヒートシール材として好適で、従来品に比べより低温で良好なヒートシール処理が可能で、且つ、容器本体構成材に対し適正な範囲の剥離強度を有すると共に、食品等容器内容物の密封保護性等この種のヒートシール材として必要とされる諸物性を従来品とほぼ同等に保持する。
然も従来品に比べより高い耐熱性と剥離時にスムーズで且つ快適な剥離感を呈する。
The resin composition for a heat seal material of the present invention is suitable as a heat seal material used for a plastic container, in particular, a container made of a plastic material such as impact-resistant polystyrene and expanded polystyrene, by the above-mentioned specific configuration, compared to conventional products. It is required as a heat seal material of this kind, such as good heat seal processing at lower temperatures and having a peel strength in an appropriate range with respect to the container body constituting material, and sealing protection of the contents of containers such as food. Maintains almost the same physical properties as conventional products.
However, it has higher heat resistance than conventional products and a smooth and comfortable peeling feeling at the time of peeling.
以下に、本発明に係る好適実施形態について、詳細且つ具体的に説明する。
本発明のヒートシール材用樹脂組成物は、エチレン・ビニルエステル共重合体樹脂(A)とエチレン・(メタ)アクリル酸エステル共重合体(B)及び粘着性付与樹脂(C)を特定量比で組合せ配合してなる。
Hereinafter, preferred embodiments according to the present invention will be described in detail and specifically.
The resin composition for a heat seal material of the present invention comprises an ethylene / vinyl ester copolymer resin (A), an ethylene / (meth) acrylic ester copolymer (B), and a tackifying resin (C) in a specific amount ratio. In combination.
本発明の樹脂組成物に於いて(A)成分であるエチレン・ビニルエステル共重合体樹脂としては、例えば、エチレンと酢酸ビニルやエチレンとプロピオン酸ビニル等のビニルエステルとの共重合体樹脂を挙げることが出来る。
本発明ではこれらの内でも、エチレン・酢酸ビニル共重合体樹脂が好ましく、特に共重合体中に存在するビニルエステル成分単位含有率(エチレン・酢酸ビニル共重合体樹脂の場合、酢酸ビニル成分単位含有率)が5〜30質量%、より好ましくは9〜28重量%、の範囲のものが好ましい。
ビニルエステル含量がこの範囲内にあると、ヒートシール強度とイージーピール性とのバランスを良好に保ち、かつ食品充填時に必要な耐熱性を有しているので好都合である。
Examples of the ethylene / vinyl ester copolymer resin as component (A) in the resin composition of the present invention include copolymer resins of ethylene and vinyl acetate such as vinyl acetate or ethylene and vinyl propionate. I can do it.
Among these, ethylene / vinyl acetate copolymer resin is preferred in the present invention, and in particular, the content of vinyl ester component units present in the copolymer (in the case of ethylene / vinyl acetate copolymer resin, vinyl acetate component unit content). The ratio is preferably in the range of 5 to 30% by weight, more preferably 9 to 28% by weight.
A vinyl ester content within this range is advantageous because it maintains a good balance between heat seal strength and easy peel properties and has the heat resistance required for filling foods.
また、この共重合体樹脂のメルトフローレート(JIS K7210−1999に準拠して測定、MFR:190℃、2160g荷重)は、その押出加工性や機械的強度の観点から、通常0.1〜100、好ましくは1〜50g/10分である。 Further, the melt flow rate (measured according to JIS K7210-1999, MFR: 190 ° C., 2160 g load) of this copolymer resin is usually 0.1 to 100, preferably from the viewpoint of extrusion processability and mechanical strength. Is 1 to 50 g / 10 min.
次に、本発明の樹脂組成物の(B)成分であるエチレン・(メタ)アクリル酸エステル共重合体樹脂に於いて(メタ)アクリル酸エステルは、アクリル酸エステル及び/又はメタクリル酸エステルを意味する。 Next, in the ethylene / (meth) acrylate copolymer resin that is the component (B) of the resin composition of the present invention, (meth) acrylate means acrylic ester and / or methacrylate. To do.
該共重合体樹脂(B)の(メタ)アクリル酸エステル単位として具体的には、アクリル酸メチル、アクリル酸エチル、アクリル酸n−プロピル、アクリル酸イソプロピル、アクリル酸n−ブチル、アクリル酸イソブチル、アクリル酸n−ヘキシル、アクリル酸イソヘキシル、アクリル酸n−オクチル、アクリル酸イソオクチル、アクリル酸−2−エチルヘキシル、メタクリル酸メチル、メタクリル酸エチル、メタクリル酸n−プロピル、メタクリル酸イソプロピル、メタクリル酸n−ブチル、メタクリル酸イソブチル、メタクリル酸n−ヘキシル、メタクリル酸イソヘキシル、メタクリル酸n−オクチル、メタクリル酸イソオクチル、メタクリル酸−2−エチルヘキシル等からなる単位を例示することができる。 Specific examples of the (meth) acrylate unit of the copolymer resin (B) include methyl acrylate, ethyl acrylate, n-propyl acrylate, isopropyl acrylate, n-butyl acrylate, isobutyl acrylate, N-hexyl acrylate, isohexyl acrylate, n-octyl acrylate, isooctyl acrylate, 2-ethylhexyl acrylate, methyl methacrylate, ethyl methacrylate, n-propyl methacrylate, isopropyl methacrylate, n-butyl methacrylate And units composed of isobutyl methacrylate, n-hexyl methacrylate, isohexyl methacrylate, n-octyl methacrylate, isooctyl methacrylate, 2-ethylhexyl methacrylate, and the like.
又、共重合体樹脂(B)のメルトフローレート(MFR:JIS K7210−1999に準拠して測定、190℃、2160g荷重)は0.1〜100g/10分であることが、それを配合して得られる組成物のヒートシール材としての特性や加工性の点から好ましく、特に1〜50g/10分が好ましい。 Further, the melt flow rate (MFR: measured in accordance with JIS K7210-1999, 190 ° C., 2160 g load) of the copolymer resin (B) is 0.1 to 100 g / 10 min. From the viewpoint of the properties and processability of the resulting composition as a heat seal material, 1 to 50 g / 10 min is particularly preferred.
更に、共重合体樹脂(B)の(メタ)アクリル酸エステル単位含量は2〜48質量%の範囲が好ましく、特に3〜40質量%の範囲が好ましい。
前記エステル単位含量が2質量%未満のものはヒートシール材として耐衝撃性ポリスチレン、発泡ポリスチレン等のプラスチック容器本体構成材に対するシール性や剥離時感触が充分でなくなり、一方48質量%を超えるものは、例え、下記に説明するチューブラー高圧重合法で製造されたものであっても耐熱性や耐熱油性の良好な共重合体を得ることが難しい。
Furthermore, the (meth) acrylic acid ester unit content of the copolymer resin (B) is preferably in the range of 2 to 48% by mass, particularly preferably in the range of 3 to 40% by mass.
When the ester unit content is less than 2% by mass, the heat sealing material has no sufficient sealing performance against the plastic container body constituting material such as high-impact polystyrene and expanded polystyrene, and the feel when peeled off. Even if it is produced by the tubular high pressure polymerization method described below, it is difficult to obtain a copolymer having good heat resistance and heat oil resistance.
本発明においては、上記エチレン・(メタ)アクリル酸エステル共重合体樹脂(B)はオートクレーブ高圧重合法、チューブラー高圧重合法 いずれの方法によって製造されたものであってもよいが、特に、チューブラー高圧重合法により製造された共重合体樹脂を用いることが好ましい。
この方法で得られた共重合体樹脂は、通常のラジカル重合法等の他の方法で製造されたエチレン・(メタ)アクリル酸エステル共重合体に比較して、例え共重合組成や平均分子量が同じものであっても融点が高く、然も、軟化〜溶融状態での粘弾性挙動等の熱的諸物性やその他の属性が異なり、このためそれを配合して得られた組成物は前述した本発明の組成物の特性をより良好に発現することが出来る。
In the present invention, the ethylene / (meth) acrylic acid ester copolymer resin (B) may be produced by either autoclave high pressure polymerization method or tubular high pressure polymerization method. It is preferable to use a copolymer resin produced by a high pressure polymerization method.
The copolymer resin obtained by this method has, for example, a copolymer composition and an average molecular weight as compared with an ethylene / (meth) acrylate copolymer produced by another method such as a normal radical polymerization method. Even if they are the same, the melting point is high, but the thermal physical properties such as viscoelastic behavior in the softened to molten state and other attributes are different. Therefore, the composition obtained by blending it is described above. The characteristics of the composition of the present invention can be expressed better.
チューブラー高圧重合法とは、チューブラー反応器を使用し、高圧で遊離基触媒を用いてラジカル重合する方法であり、例えば、特開昭62−273214号公報等に記載されている方法が例示できる。 The tubular high pressure polymerization method is a method of radical polymerization using a free radical catalyst at a high pressure using a tubular reactor, for example, a method described in JP-A-62-273214 and the like. it can.
上記重合法で得られた共重合体は、(メタ)アクリル酸エステル含量:E(重量%)と共重合体融点:T(℃)との関係が下記式(I)、
−0.8×E+115≧T≧−0.8×E+109…(I)
を満足することが特徴であって、他の重合法で得られた相当組成の共重合体に比べて融点が高く耐熱性に優れる。
上記重合法で得られた共重合体は通常のラジカル重合法によるランダム性良好な共重合体に比較して、エチレン単位や(メタ)アクリル酸エステル単位のランダム配列が少なく、即ち、配列不均一性が高く、ブロック共重合体にやや似た重合体構造、物性を有する。
このため融点とエステル単位含量が上記のような関係を有するものと考えられる。
The copolymer obtained by the above polymerization method has a relationship between (meth) acrylic acid ester content: E (% by weight) and copolymer melting point: T (° C.) represented by the following formula (I),
−0.8 × E + 115 ≧ T ≧ −0.8 × E + 109 (I)
And has a high melting point and excellent heat resistance as compared with a copolymer having an equivalent composition obtained by another polymerization method.
The copolymer obtained by the above polymerization method has less random arrangement of ethylene units and (meth) acrylic acid ester units than that of a copolymer having good randomness by a normal radical polymerization method, that is, the arrangement is not uniform. The polymer structure and physical properties are somewhat similar to those of block copolymers.
For this reason, it is thought that melting | fusing point and ester unit content have the above relationships.
上記重合法に於ける遊離基触媒としては、ペルオキシド、ヒドロペルオキシド、アゾ化合物、アミンオキシド化合物、酸素等の通常の開始剤を挙げることが出来る。
又、連鎖移動剤としては水素、プロピレン、ブテン−1、C1〜C20又はそれ以上の飽和脂肪族炭化水素及びハロゲン置換炭化水素、例えばメタン、エタン、プロパン、ブタン、イソブタン、n−ヘキサン、n−ヘプタン、シクロパラフィン類、クロロホルム及び四塩化炭素、C1〜C20又はそれ以上の飽和脂肪族アルコール、例えば、メタノール、エタノール、プロパノール及びイソプロパノール、C1〜C20又はそれ以上の飽和脂肪族カルボニル化合物、例えば二酸化炭素、アセトン及びメチルエチルケトン並びに芳香族化合物、例えばトルエン、エチルベンゼン及びキシレンのような化合物が挙げられる。
Examples of the free radical catalyst in the polymerization method include ordinary initiators such as peroxides, hydroperoxides, azo compounds, amine oxide compounds, and oxygen.
Chain transfer agents include hydrogen, propylene, butene-1, C 1 -C 20 or more saturated aliphatic hydrocarbons and halogen-substituted hydrocarbons such as methane, ethane, propane, butane, isobutane, n-hexane, n- heptane, cycloparaffins, chloroform and carbon tetrachloride, C 1 -C 20 or higher saturated aliphatic alcohols, such as methanol, ethanol, propanol and isopropanol, C 1 -C 20 or higher saturated aliphatic Examples include carbonyl compounds such as carbon dioxide, acetone and methyl ethyl ketone and aromatic compounds such as toluene, ethylbenzene and xylene.
本発明の樹脂組成物の(C)成分である粘着性付与樹脂としては、脂肪族系炭化水素樹脂、脂環族系炭化水素樹脂、芳香族系炭化水素樹脂、ポリテルペン系樹脂、ロジン類、スチレン系樹脂、クマロン・インデン樹脂などの他、石油ナフサの熱分解留分から得られる石油樹脂やその水素添加物を挙げることができる。 Examples of the tackifying resin that is the component (C) of the resin composition of the present invention include aliphatic hydrocarbon resins, alicyclic hydrocarbon resins, aromatic hydrocarbon resins, polyterpene resins, rosins, and styrene. In addition to petroleum resins, coumarone / indene resins, etc., petroleum resins obtained from the thermal decomposition fraction of petroleum naphtha and hydrogenated products thereof can be mentioned.
脂肪族炭化水素樹脂の例としては、1−ブテン、イソブテン、ブタジエン、1,3−ペンタジエン、イソプレンなどの炭素数4〜5のモノ又はジオレフィンの少なくとも一種以上を含む留分を重合して得られる樹脂を挙げることができる。 Examples of the aliphatic hydrocarbon resin are obtained by polymerizing a fraction containing at least one mono- or diolefin having 4 to 5 carbon atoms such as 1-butene, isobutene, butadiene, 1,3-pentadiene, and isoprene. Resins that can be used.
又、脂環族系炭化水素樹脂の例として、スペントC4〜C5留分中のジエン成分を環化二量化後重合させて得られる樹脂、シクロペンタジエンなどの環状モノマーを重合させた樹脂、芳香族系炭化水素樹脂を核内水添した樹脂などを挙げることができる。 Examples of alicyclic hydrocarbon resins include resins obtained by polymerizing diene components in spent C4 to C5 fractions after cyclization and dimerization, resins obtained by polymerizing cyclic monomers such as cyclopentadiene, aromatics Examples thereof include a resin obtained by hydrogenating a hydrocarbon-based hydrocarbon resin.
芳香族系炭化水素樹脂の例として、ビニルトルエン、インデン、α−メチルスチレンなどのC8〜C10のビニル芳香族炭化水素を少なくとも一種以上含有する留分を重合して得られる樹脂、あるいはこれら留分と上記脂肪族炭化水素留分を共重合して得られる樹脂などを挙げることができる。
ポリテルペン系樹脂の例としては、α−ピネン重合体、β−ピネン重合体、ジペンテン重合体、テルペン・フェノール共重合体、α−ピネン・フェノール共重合体などを挙げることができる。
Examples of aromatic hydrocarbon resins include resins obtained by polymerizing a fraction containing at least one C8-C10 vinyl aromatic hydrocarbon such as vinyltoluene, indene, α-methylstyrene, or the like. And resins obtained by copolymerizing the above aliphatic hydrocarbon fractions.
Examples of polyterpene resins include α-pinene polymers, β-pinene polymers, dipentene polymers, terpene / phenol copolymers, α-pinene / phenol copolymers, and the like.
ロジン類としては、ガムロジン、ウッドロジン、トール油などのロジン及びその変性物などであり、変性物としては水素添加、不均化、二量化、エステル化などの変性を施したものを例示することができる。
スチレン系炭化水素樹脂としては、純度の高いスチレン、ビニルトルエン、α−メチルスチレン、イソプロピルトルエンなどのスチレン系単量体の一種又は二種以上を重合して得られる分子量の低い樹脂状重合体を挙げることができる。
Examples of rosins include rosins such as gum rosin, wood rosin and tall oil, and modified products thereof. Examples of modified products include those subjected to modification such as hydrogenation, disproportionation, dimerization, and esterification. it can.
As the styrenic hydrocarbon resin, a low molecular weight resinous polymer obtained by polymerizing one or more styrene monomers such as high-purity styrene, vinyltoluene, α-methylstyrene, and isopropyltoluene. Can be mentioned.
石油樹脂は、石油ナフサの熱分解により、エチレン、プロピレン、ブタジエン等を分留した残りのスペントC5〜C9留分のオレフィンを、混合状態のまま重合して得られた樹脂状物質の総称であるが、その主成分組成により脂肪族系、芳香族系、ジシクロペンタン系等があり、その組成、性状は、それぞれ既に述べた脂肪族系炭化水素樹脂、脂環族系炭化水素樹脂、芳香族系炭化水素樹脂に類似する。
芳香族系やジシクロペンタン系のものは特にエチレン・ビニルエステル共重合体樹脂との相溶性がよい。
又、これら石油樹脂を水素添加して得られた物は樹脂の色調や臭気が改善されるだけでなく流動性も向上し粘着性付与樹脂として特に好適である。
Petroleum resin, by the thermal decomposition of petroleum naphtha, ethylene, propylene, olefins remaining spent C 5 -C 9 fraction obtained by fractionating butadiene, generic name for the resulting resinous material by polymerizing remain mixed state However, the main component composition includes aliphatic, aromatic, dicyclopentane, etc., and the composition and properties of the aliphatic hydrocarbon resin, alicyclic hydrocarbon resin already described, Similar to aromatic hydrocarbon resin.
Aromatic and dicyclopentane types are particularly compatible with ethylene / vinyl ester copolymer resins.
Further, those obtained by hydrogenating these petroleum resins are not only improved in the color tone and odor of the resin, but also improved in fluidity, and are particularly suitable as tackifying resins.
本発明の樹脂組成物には、前記本発明のヒートシール特性を害しない限りに於いて、必要により任意の樹脂成分、例えば、エチレン・(メタ)アクリル酸共重合体、エチレン・エタクリル酸共重合体、エチレンマレイン酸共重合体、エチレン・フマル酸共重合体等のエチレン不飽和カルボン酸共重合体樹脂、ポリエチレン、ポリプロピレン、ポリブテン、エチレン・αオレフィン共重合体等のポリオレフィン系樹脂類等を配合することが出来る。 The resin composition of the present invention may contain any resin component such as an ethylene / (meth) acrylic acid copolymer, an ethylene / ethacrylic acid copolymer as long as it does not impair the heat seal characteristics of the present invention. Compound, ethylene maleic acid copolymer, ethylene unsaturated carboxylic acid copolymer resin such as ethylene / fumaric acid copolymer, polyolefin resin such as polyethylene, polypropylene, polybutene, ethylene / α-olefin copolymer, etc. I can do it.
本発明の樹脂組成物における上記必須樹脂成分(A)、(B)、(C)の配合割合は、エチレン・ビニルエステル共重合体樹脂(A)30〜80質量部、好ましくは35〜75質量部、エチレン・(メタ)アクリル酸エステル共重合体樹脂(B)1〜45質量部、好ましくは5〜40質量部、及び、粘着性付与樹脂(C)3〜30質量部、好ましくは5〜25質量部(但し(A)、(B)、(C)樹脂の合計量は100質量部)である。 The blending ratio of the essential resin components (A), (B), and (C) in the resin composition of the present invention is 30 to 80 parts by mass, preferably 35 to 75 parts by mass, of the ethylene / vinyl ester copolymer resin (A). Parts, ethylene / (meth) acrylic acid ester copolymer resin (B) 1 to 45 parts by mass, preferably 5 to 40 parts by mass, and tackifier resin (C) 3 to 30 parts by mass, preferably 5 to 25 parts by mass (however, the total amount of (A), (B), (C) resin is 100 parts by mass).
エチレン・ビニルエステル共重合体樹脂(A)の配合量が80質量部を上回ると、得られる樹脂組成物の耐熱性が悪化するだけでなく、ヒートシール強度の温度依存性も大きくなりすぎるため好ましくない。
一方、エチレン・ビニルエステル共重合体樹脂(A)の配合量が30質量部を下回ると、容器構成材に対するシール強度が大きくならず、密封性に問題を生じる。
When the blending amount of the ethylene / vinyl ester copolymer resin (A) exceeds 80 parts by mass, not only the heat resistance of the resulting resin composition is deteriorated, but also the temperature dependency of the heat seal strength is preferably increased. Absent.
On the other hand, when the blending amount of the ethylene / vinyl ester copolymer resin (A) is less than 30 parts by mass, the sealing strength with respect to the container constituent material is not increased, which causes a problem in sealing performance.
又、エチレン・(メタ)アクリル酸エステル共重合体樹脂(B)配合量が45質量部を上回ると、前記エチレン・ビニルエステル共重合体樹脂(A)の場合と同様、耐衝撃性ポリスチレン、発泡ポリスチレン等の容器構成材に対するヒートシール強度が強くなりすぎ、開封性も悪化するのみならず、ヒートシール強度の温度依存性も大きくなりすぎるため好ましくない。
一方、(B)成分の配合量が上記下限を下回るものは、配合量が少なすぎるため本発明の組成物の特徴である低温ヒートシール性、適正剥離強度、容器内容物の密封保護性等の諸特性を具現出来ず、又、剥離時にスムーズで且つ快適な剥離感を呈することが出来ない。
Further, when the blending amount of the ethylene / (meth) acrylic acid ester copolymer resin (B) exceeds 45 parts by mass, as in the case of the ethylene / vinyl ester copolymer resin (A), high impact polystyrene, foaming This is not preferable because the heat seal strength for container components such as polystyrene becomes too strong and the unsealing property deteriorates, and the temperature dependence of the heat seal strength becomes too large.
On the other hand, when the blending amount of the component (B) is less than the above lower limit, the blending amount is too small, such as the low-temperature heat-sealability, proper peel strength, and sealing protection of the container contents, which are the characteristics of the composition of the present invention. Various characteristics cannot be realized, and a smooth and comfortable peeling feeling cannot be exhibited at the time of peeling.
粘着性付与樹脂(C)の配合量が30質量部を上回るものは、得られる樹脂組成物のブロッキングが著しくなりペレット化が困難となる。
又、シール材としてのシール強度も強くなりすぎるだけでなく、食品包装用途等の場合においては油抽出分が多くなるため好ましくない。
一方配合量が3質量%を下回る場合は、シール強度が適正値より低くなる傾向を示し、特に、低温シール性が悪化する。
When the compounding amount of the tackifying resin (C) exceeds 30 parts by mass, the resulting resin composition is remarkably blocked and becomes difficult to be pelletized.
In addition, not only is the sealing strength as a sealing material too strong, but in the case of food packaging applications, etc., it is not preferable because the amount of oil extraction increases.
On the other hand, when the blending amount is less than 3% by mass, the seal strength tends to be lower than an appropriate value, and in particular, the low-temperature sealability is deteriorated.
尚、任意成分として他の樹脂成分を配合する場合は、前記(A)、(B)、(C)合計量100質量部に対し1〜30質量部程度が好ましい。 In addition, when mix | blending another resin component as an arbitrary component, about 1-30 mass parts is preferable with respect to 100 mass parts of said (A), (B), (C) total amount.
本発明の樹脂組成物においては、必要に応じて更に各種添加剤を配合することができる。
かかる添加剤の代表例としては、押出加工性、離ロール性、フイルムの滑り性などの改善の目的で使用される滑剤及び/又は離ロール剤を挙げることができる。
In the resin composition of the present invention, various additives can be further blended as necessary.
Representative examples of such additives include lubricants and / or roll releasing agents used for the purpose of improving extrudability, roll releasing properties, film slipping properties, and the like.
より具体的には、パルミチン酸アミド、ステアリン酸アミド、ベヘニン酸アミド、オレイン酸アミド、エルカ酸アミド、オレイルパルミドアミド、ステアリルパルミドアミド、メチレンビスステアリルアミド、メチレンビスオレイルアミド、エチレンビスエルカ酸アミドなどの各種アミド類、ポリエチレングリコール、ポリプロピレングリコールなどのポリアルキレングリコール、水添ひまし油、シリカ、タルク、ゼオライトなどの無機質添加剤などである。
これらの配合量は、樹脂成分量に対し無機質添加剤の場合は0.1〜3質量%程度、それ以外のものは0.01〜1質量%程度の範囲が適当である。
More specifically, palmitic acid amide, stearic acid amide, behenic acid amide, oleic acid amide, erucic acid amide, oleyl palmidamide, stearyl palmamide, methylenebisstearylamide, methylenebisoleylamide, ethylenebiserucamide, etc. Various amides, polyalkylene glycols such as polyethylene glycol and polypropylene glycol, hydrogenated castor oil, silica, talc, zeolite and other inorganic additives.
These blending amounts are suitably in the range of about 0.1 to 3% by mass in the case of an inorganic additive and about 0.01 to 1% by mass for the other components with respect to the resin component amount.
本発明の樹脂組成物は、上記(A)、(B)、(C)の各必須樹脂成分、及び任意に配合される樹脂成分や添加剤を、同時に又は逐次的に混合することによって調製することができる。
樹脂組成物を調製するに当たっては、単軸押出機、二軸押出機、バンバリーミキサー、各種ニーダーなどを用いて溶融混合するのが好ましく、その混合順序にはとくに制限はない。
The resin composition of the present invention is prepared by mixing the essential resin components (A), (B), and (C) described above, and optionally blended resin components and additives simultaneously or sequentially. be able to.
In preparing the resin composition, it is preferable to melt and mix using a single screw extruder, a twin screw extruder, a Banbury mixer, various kneaders, and the mixing order is not particularly limited.
かくして得られる本発明の樹脂組成物は、押出加工性、シール強度、耐ボイル性等を考慮すると、190℃、2160g荷重におけるメルトフローレートが0.1〜100g/10分、とくに1〜30g/10分程度となるように調製されていることが望ましい。 The resin composition of the present invention thus obtained has a melt flow rate of 0.1 to 100 g / 10 min, particularly 1 to 30 g / min at 190 ° C. under a load of 2160 g in consideration of extrudability, seal strength, boil resistance and the like. It is desirable that it is prepared so as to be about 10 minutes.
本発明の樹脂組成物は、プラスチック製容器のヒートシール材、とりわけ耐衝撃性ポリスチレンや発泡ポリスチレン等の容器とその蓋材との易開封性シール材料として好適である。 The resin composition of the present invention is suitable as a heat-sealing material for plastic containers, particularly as an easily openable sealing material for containers such as impact-resistant polystyrene and foamed polystyrene and its lid material.
又、本発明のヒートシール性樹脂組成物は、このような用途に使用される場合、通常は各種基材に積層した形で使用される。
かかる目的に使用される基材としては、紙、アルミニウム、ポリエステル、ポリエチレン、ポリプロピレン、(高衝撃)ポリスチレン、アルミ蒸着ポリエステル、アルミ蒸着ポリプロピレン、シリカ蒸着ポリエステルなどを挙げることができる。
このような基材は単層である必要はなく、2層以上の積層体であってもよい。
Moreover, when the heat-sealable resin composition of the present invention is used for such applications, it is usually used in a form laminated on various substrates.
Examples of the base material used for this purpose include paper, aluminum, polyester, polyethylene, polypropylene, (high impact) polystyrene, aluminum-deposited polyester, aluminum-deposited polypropylene, and silica-deposited polyester.
Such a substrate need not be a single layer, and may be a laminate of two or more layers.
かくして得られる積層体は、各種包装材料として使用することができる。
本発明のヒートシール性樹脂組成物は、プラスチック単体や上述のような積層体からなる各種の易開封シール蓋付き容器、とりわけ耐衝撃性ポリスチレン容器と蓋材との間のヒートシール材として使用するときに密封性、易開封性等に優れたものとなる。
更にポリスチレン製容器のみならず、他の材料の容器、例えば、ポリプロピレン、ポリエステル、ポリカーボネート、ポリ塩化ビニル等の容器と蓋材のヒートシール用として有効に利用できる。
このような蓋付容器は、例えば、即席メン、ヌードル、ゼリー、プリン、ヨーグルト、みつ豆、サワー、豆腐、乳酸飲料、和菓子、加工肉などの飲食物、薬品、医療容器、トナーなどの各種包装に使用することができる。
The laminate thus obtained can be used as various packaging materials.
The heat-sealable resin composition of the present invention is used as a heat-seal material between a single plastic or various easy-open seal-covered containers made of the above-described laminate, particularly between an impact-resistant polystyrene container and a cover material. Sometimes it has excellent sealing properties, easy opening properties, and the like.
Furthermore, it can be effectively used not only for a container made of polystyrene but also for a container of other materials, for example, a container for polypropylene, polyester, polycarbonate, polyvinyl chloride, etc. and a heat seal for a lid.
Such lidded containers can be used for various types of packaging such as instant men, noodles, jelly, pudding, yogurt, honey beans, sour, tofu, lactic acid beverages, Japanese confectionery, processed meats, medicines, medical containers, toners, etc. Can be used.
本発明を次の実施例により具体的に説明するが、本発明はこれら実施例により何ら限定されるものではない。
尚、下記の実施例、比較例で用いたエチレン・ビニルエステル共重合体樹脂(エチレン・酢酸ビニル共重合体樹脂)(A)、エチレン・(メタ)アクリル酸エステル共重合体樹脂(エチレン・アクリル酸メチル共重合体樹脂)(B)及び粘着性付与樹脂(水素添加石油樹脂)(C)、その他樹脂、及び、各種添加剤の組成、性状はそれぞれ下記の通りである。
The present invention will be specifically described by the following examples, but the present invention is not limited to these examples.
The ethylene / vinyl ester copolymer resin (ethylene / vinyl acetate copolymer resin) (A), ethylene / (meth) acrylic acid ester copolymer resin (ethylene / acrylic) used in the following examples and comparative examples. The composition and properties of acid methyl copolymer resin (B), tackifier resin (hydrogenated petroleum resin) (C), other resins, and various additives are as follows.
1) エチレン・酢酸ビニル共重合体樹脂(EVA):酢酸ビニル成分含量9.1質量%、MFR(190℃、2160g荷重)1.7g/10分
2) エチレン・アクリル酸メチル共重合体樹脂(EMA):アクリル酸メチル成分含量18質量%、MFR(190℃、2160g荷重)2.0g/10分
3) 水素添加石油樹脂(AM1):
4)ポリエチレン(PE):低密度ポリエチレン、MFR3.8g/10分、密度903kg/m3
5) ステアリン酸アミド(AHT)
6) エルカ酸アミド(ELA)
7) 合成ゼオライト
1) Ethylene / vinyl acetate copolymer resin (EVA): vinyl acetate component content 9.1% by mass, MFR (190 ° C., 2160 g load) 1.7 g / 10 min 2) Ethylene / methyl acrylate copolymer resin ( EMA): Methyl acrylate component content 18% by mass, MFR (190 ° C., 2160 g load) 2.0 g / 10 min 3) Hydrogenated petroleum resin (AM1):
4) Polyethylene (PE): low density polyethylene, MFR 3.8 g / 10 min, density 903 kg / m 3
5) Stearic acid amide (AHT)
6) Erucamide (ELA)
7) Synthetic zeolite
「実施例1」
(A)成分として上記EVAを63質量部、(B)成分としてEMAを10質量部、(C)成分としてAM1を15質量部及びPEを10質量部配合したものを溶融混合し、これに添加剤としてAHT(ステアリン酸アミド)0.15質量部とELA(エルカ酸アミド)0.15質量部と合成ゼオライト粉末1質量部を添加して樹脂組成物(組成物1)を得た。
この樹脂組成物(組成物1)を加工温度240℃、加工速度80m/分で押出ラミネート加工によりポリエチレンテレフタレート基材層(PET:12μm)/ポリエチレン層(PE:20μm)/組成物1の層(50μm)の積層体を得た。
この積層体(組成物1の積層体)を耐衝撃性ポリスチレンシート(厚さ2mm)縁面上に下記条件でヒートシールし、24時間放置後剥離試験(180°、15mm幅剥離)を実施した。
ヒートシール条件:0.2MPa×0.5sec×120〜160℃
各ヒートシール温度条件での剥離強度を表1に示す。
"Example 1"
(A) 63 parts by mass of the above EVA as the component, 10 parts by mass of EMA as the (B) component, 15 parts by mass of AM1 and 10 parts by mass of PE as the (C) component are melt mixed and added to this As the agent, 0.15 parts by mass of AHT (stearic amide), 0.15 parts by mass of ELA (erucic amide) and 1 part by mass of synthetic zeolite powder were added to obtain a resin composition (Composition 1).
This resin composition (Composition 1) was subjected to extrusion lamination at a processing temperature of 240 ° C. and a processing speed of 80 m / min to obtain a polyethylene terephthalate base layer (PET: 12 μm) / polyethylene layer (PE: 20 μm) / composition 1 layer ( 50 μm) was obtained.
This laminate (laminate of composition 1) was heat-sealed on the edge surface of an impact-resistant polystyrene sheet (thickness 2 mm) under the following conditions, and left for 24 hours and then subjected to a peel test (180 °, 15 mm width peel). .
Heat sealing conditions: 0.2 MPa × 0.5 sec × 120-160 ° C.
Table 1 shows the peel strength under each heat seal temperature condition.
「比較例1」
(A)成分としてEVAを73質量部、(C)成分としてAM1を15質量部及びPEを10質量部配合して溶融混合し、これに添加剤としてAHT0.15質量部とELA0.15質量部と合成ゼオライト粉末1質量部を添加して樹脂組成物(組成物2)を得た。
この樹脂組成物(組成物2)を用いて実施例1と同様に処理し、組成物2の層(50μm)を有する積層体を得た。
この積層体(組成物2の積層体)を実施例1と同様の耐衝撃性ポリスチレン容器縁面上に下記条件でヒートシールし、24時間放置後剥離試験(180°、15mm幅剥離)を実施した。
ヒートシール条件:0.2MPa×1.0sec×120〜160℃
各ヒートシール温度条件での剥離強度を表1に示す。
"Comparative Example 1"
(A) 73 parts by mass of EVA as component, 15 parts by mass of AM1 and (10) parts by mass of PE as component (C), and melt mixed, 0.15 parts by mass of AHT and 0.15 parts by mass of ELA as additives And 1 part by mass of synthetic zeolite powder were added to obtain a resin composition (Composition 2).
Using this resin composition (Composition 2), the same treatment as in Example 1 was carried out to obtain a laminate having a layer (50 μm) of Composition 2.
This laminate (laminate of composition 2) was heat-sealed on the edge of the same impact-resistant polystyrene container as in Example 1 under the following conditions, and left for 24 hours before being subjected to a peel test (180 °, 15 mm width peel). did.
Heat sealing conditions: 0.2 MPa × 1.0 sec × 120 to 160 ° C.
Table 1 shows the peel strength under each heat seal temperature condition.
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WO2019188691A1 (en) * | 2018-03-30 | 2019-10-03 | 三井・ダウ ポリケミカル株式会社 | Resin composition for sealant, lid, and package |
WO2020110829A1 (en) | 2018-11-30 | 2020-06-04 | 三井・ダウ ポリケミカル株式会社 | Resin composition for sealant, layered body, packaging material and packaging body |
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CN107207927A (en) * | 2015-02-09 | 2017-09-26 | 三井—杜邦聚合化学株式会社 | Adhesive resin and release performance film |
JPWO2016129567A1 (en) * | 2015-02-09 | 2017-11-16 | 三井・デュポンポリケミカル株式会社 | Adhesive resin and easily peelable film |
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WO2019188691A1 (en) * | 2018-03-30 | 2019-10-03 | 三井・ダウ ポリケミカル株式会社 | Resin composition for sealant, lid, and package |
CN111742030A (en) * | 2018-03-30 | 2020-10-02 | 三井—陶氏聚合化学株式会社 | Resin composition for sealing agent, lid material, and package |
JPWO2019188691A1 (en) * | 2018-03-30 | 2021-04-30 | 三井・ダウポリケミカル株式会社 | Sealant resin composition, lid material, and packaging |
CN111742030B (en) * | 2018-03-30 | 2023-05-12 | 三井—陶氏聚合化学株式会社 | Resin composition for sealant, cover material, and package |
WO2020110829A1 (en) | 2018-11-30 | 2020-06-04 | 三井・ダウ ポリケミカル株式会社 | Resin composition for sealant, layered body, packaging material and packaging body |
US11898065B2 (en) | 2018-11-30 | 2024-02-13 | Dow-Mitsui Polychemicals Co., Ltd. | Resin composition for sealant, laminate, packaging material, and package |
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