JPH02130119A - Laminated film and manufacture thereof - Google Patents
Laminated film and manufacture thereofInfo
- Publication number
- JPH02130119A JPH02130119A JP63283891A JP28389188A JPH02130119A JP H02130119 A JPH02130119 A JP H02130119A JP 63283891 A JP63283891 A JP 63283891A JP 28389188 A JP28389188 A JP 28389188A JP H02130119 A JPH02130119 A JP H02130119A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- film
- die
- annular
- laminated film
- 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
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 11
- 229920005989 resin Polymers 0.000 claims abstract description 123
- 239000011347 resin Substances 0.000 claims abstract description 123
- 230000000903 blocking effect Effects 0.000 claims abstract description 32
- 238000010438 heat treatment Methods 0.000 claims abstract description 25
- 229920001684 low density polyethylene Polymers 0.000 abstract description 22
- 239000004702 low-density polyethylene Substances 0.000 abstract description 22
- 239000000853 adhesive Substances 0.000 abstract description 14
- 230000001070 adhesive effect Effects 0.000 abstract description 13
- 238000000034 method Methods 0.000 abstract description 13
- 238000000465 moulding Methods 0.000 abstract description 13
- 230000000694 effects Effects 0.000 abstract description 11
- 239000011342 resin composition Substances 0.000 abstract description 11
- 229920001903 high density polyethylene Polymers 0.000 abstract description 10
- 239000004700 high-density polyethylene Substances 0.000 abstract description 10
- 238000001816 cooling Methods 0.000 abstract description 8
- 230000008569 process Effects 0.000 abstract description 5
- 239000000203 mixture Substances 0.000 abstract description 3
- 239000010410 layer Substances 0.000 description 50
- 239000000463 material Substances 0.000 description 22
- 239000006229 carbon black Substances 0.000 description 14
- 235000019241 carbon black Nutrition 0.000 description 14
- -1 and conventionally Substances 0.000 description 12
- 239000000314 lubricant Substances 0.000 description 11
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
- 239000000126 substance Substances 0.000 description 9
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 7
- 239000005022 packaging material Substances 0.000 description 7
- 238000007789 sealing Methods 0.000 description 7
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 239000002356 single layer Substances 0.000 description 6
- 229920005992 thermoplastic resin Polymers 0.000 description 6
- 239000012790 adhesive layer Substances 0.000 description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- 239000003963 antioxidant agent Substances 0.000 description 5
- 230000003078 antioxidant effect Effects 0.000 description 5
- 229920001038 ethylene copolymer Polymers 0.000 description 5
- 239000000049 pigment Substances 0.000 description 5
- 239000000654 additive Substances 0.000 description 4
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 4
- 239000005038 ethylene vinyl acetate Substances 0.000 description 4
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- 239000004925 Acrylic resin Substances 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- 239000004594 Masterbatch (MB) Substances 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- 229910000019 calcium carbonate Inorganic materials 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 230000006866 deterioration Effects 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 229920006226 ethylene-acrylic acid Polymers 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 238000003475 lamination Methods 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- FATBGEAMYMYZAF-KTKRTIGZSA-N oleamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(N)=O FATBGEAMYMYZAF-KTKRTIGZSA-N 0.000 description 3
- 238000004806 packaging method and process Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 150000003014 phosphoric acid esters Chemical class 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
- 239000000454 talc Substances 0.000 description 3
- 229910052623 talc Inorganic materials 0.000 description 3
- 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 2
- FWLHAQYOFMQTHQ-UHFFFAOYSA-N 2-N-[8-[[8-(4-aminoanilino)-10-phenylphenazin-10-ium-2-yl]amino]-10-phenylphenazin-10-ium-2-yl]-8-N,10-diphenylphenazin-10-ium-2,8-diamine hydroxy-oxido-dioxochromium Chemical compound O[Cr]([O-])(=O)=O.O[Cr]([O-])(=O)=O.O[Cr]([O-])(=O)=O.Nc1ccc(Nc2ccc3nc4ccc(Nc5ccc6nc7ccc(Nc8ccc9nc%10ccc(Nc%11ccccc%11)cc%10[n+](-c%10ccccc%10)c9c8)cc7[n+](-c7ccccc7)c6c5)cc4[n+](-c4ccccc4)c3c2)cc1 FWLHAQYOFMQTHQ-UHFFFAOYSA-N 0.000 description 2
- KUDUQBURMYMBIJ-UHFFFAOYSA-N 2-prop-2-enoyloxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC(=O)C=C KUDUQBURMYMBIJ-UHFFFAOYSA-N 0.000 description 2
- XOUQAVYLRNOXDO-UHFFFAOYSA-N 2-tert-butyl-5-methylphenol Chemical compound CC1=CC=C(C(C)(C)C)C(O)=C1 XOUQAVYLRNOXDO-UHFFFAOYSA-N 0.000 description 2
- 241000251468 Actinopterygii Species 0.000 description 2
- 239000004604 Blowing Agent Substances 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
- CJPQIRJHIZUAQP-MRXNPFEDSA-N benalaxyl-M Chemical compound CC=1C=CC=C(C)C=1N([C@H](C)C(=O)OC)C(=O)CC1=CC=CC=C1 CJPQIRJHIZUAQP-MRXNPFEDSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 238000004049 embossing Methods 0.000 description 2
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 229920006244 ethylene-ethyl acrylate Polymers 0.000 description 2
- 239000005042 ethylene-ethyl acrylate Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 229920000554 ionomer Polymers 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 229920000092 linear low density polyethylene Polymers 0.000 description 2
- 239000004707 linear low-density polyethylene Substances 0.000 description 2
- 229920001179 medium density polyethylene Polymers 0.000 description 2
- 239000004701 medium-density polyethylene Substances 0.000 description 2
- 239000010445 mica Substances 0.000 description 2
- 229910052618 mica group Inorganic materials 0.000 description 2
- LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 description 2
- 229920000767 polyaniline Polymers 0.000 description 2
- 229920013716 polyethylene resin Polymers 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 239000000779 smoke Substances 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 2
- YAPRWCFMWHUXRS-UHFFFAOYSA-N (2-hydroxyphenyl) propanoate Chemical compound CCC(=O)OC1=CC=CC=C1O YAPRWCFMWHUXRS-UHFFFAOYSA-N 0.000 description 1
- QLZJUIZVJLSNDD-UHFFFAOYSA-N 2-(2-methylidenebutanoyloxy)ethyl 2-methylidenebutanoate Chemical compound CCC(=C)C(=O)OCCOC(=O)C(=C)CC QLZJUIZVJLSNDD-UHFFFAOYSA-N 0.000 description 1
- FVBBMPBYVZWAAI-UHFFFAOYSA-N 2-butyl-4-[1-(5-butyl-4-hydroxy-2-methylphenyl)butyl]-5-methylphenol Chemical compound C1=C(O)C(CCCC)=CC(C(CCC)C=2C(=CC(O)=C(CCCC)C=2)C)=C1C FVBBMPBYVZWAAI-UHFFFAOYSA-N 0.000 description 1
- IKEHOXWJQXIQAG-UHFFFAOYSA-N 2-tert-butyl-4-methylphenol Chemical compound CC1=CC=C(O)C(C(C)(C)C)=C1 IKEHOXWJQXIQAG-UHFFFAOYSA-N 0.000 description 1
- ODJQKYXPKWQWNK-UHFFFAOYSA-L 3-(2-carboxylatoethylsulfanyl)propanoate Chemical compound [O-]C(=O)CCSCCC([O-])=O ODJQKYXPKWQWNK-UHFFFAOYSA-L 0.000 description 1
- FKIOYBLZUCCLTL-UHFFFAOYSA-N 4-butyl-2-tert-butyl-5-methylphenol Chemical compound CCCCC1=CC(C(C)(C)C)=C(O)C=C1C FKIOYBLZUCCLTL-UHFFFAOYSA-N 0.000 description 1
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 1
- HEKJWPLNKNZYCA-UHFFFAOYSA-N CCCCCCCCCC(C=C1)=C(CCCCCCCCC)C(CCCCCCCCC)=C1OP(O)O.CCCCCCCCCC(C=C1)=C(CCCCCCCCC)C(CCCCCCCCC)=C1OP(O)O.CCCCCCCCCC(C=C1)=C(CCCCCCCCC)C(CCCCCCCCC)=C1OP(O)O.P.P Chemical compound CCCCCCCCCC(C=C1)=C(CCCCCCCCC)C(CCCCCCCCC)=C1OP(O)O.CCCCCCCCCC(C=C1)=C(CCCCCCCCC)C(CCCCCCCCC)=C1OP(O)O.CCCCCCCCCC(C=C1)=C(CCCCCCCCC)C(CCCCCCCCC)=C1OP(O)O.P.P HEKJWPLNKNZYCA-UHFFFAOYSA-N 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 239000004709 Chlorinated polyethylene Substances 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
- GHKOFFNLGXMVNJ-UHFFFAOYSA-N Didodecyl thiobispropanoate Chemical compound CCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCC GHKOFFNLGXMVNJ-UHFFFAOYSA-N 0.000 description 1
- 239000003508 Dilauryl thiodipropionate Substances 0.000 description 1
- 239000002656 Distearyl thiodipropionate Substances 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- 229920000571 Nylon 11 Polymers 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 206010034972 Photosensitivity reaction Diseases 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- 241000872198 Serjania polyphylla Species 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 235000010724 Wisteria floribunda Nutrition 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000006230 acetylene black Substances 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 239000002981 blocking agent Substances 0.000 description 1
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 239000001030 cadmium pigment Substances 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 239000006231 channel black Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- 230000009034 developmental inhibition Effects 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 235000019304 dilauryl thiodipropionate Nutrition 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- PWWSSIYVTQUJQQ-UHFFFAOYSA-N distearyl thiodipropionate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCCCCCCCC PWWSSIYVTQUJQQ-UHFFFAOYSA-N 0.000 description 1
- 235000019305 distearyl thiodipropionate Nutrition 0.000 description 1
- RRZCFXQTVDJDGF-UHFFFAOYSA-N dodecyl 3-(3-octadecoxy-3-oxopropyl)sulfanylpropanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCC RRZCFXQTVDJDGF-UHFFFAOYSA-N 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- UAUDZVJPLUQNMU-KTKRTIGZSA-N erucamide Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(N)=O UAUDZVJPLUQNMU-KTKRTIGZSA-N 0.000 description 1
- QHZOMAXECYYXGP-UHFFFAOYSA-N ethene;prop-2-enoic acid Chemical compound C=C.OC(=O)C=C QHZOMAXECYYXGP-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 239000006232 furnace black Substances 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 1
- 125000004464 hydroxyphenyl group Chemical group 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- 239000006078 metal deactivator Substances 0.000 description 1
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- GMYQTFXMWMSQBV-CLFAGFIQSA-N n,n'-bis[(z)-octadec-9-enyl]oxamide Chemical compound CCCCCCCC\C=C/CCCCCCCCNC(=O)C(=O)NCCCCCCCC\C=C/CCCCCCCC GMYQTFXMWMSQBV-CLFAGFIQSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- QJNLTJUIWSYOJY-UHFFFAOYSA-N octadecyl 3-(3,5-dibutyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(CCCC)=C(O)C(CCCC)=C1 QJNLTJUIWSYOJY-UHFFFAOYSA-N 0.000 description 1
- SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 description 1
- GJNDMSSZEBNLPU-UHFFFAOYSA-N octadecylurea Chemical compound CCCCCCCCCCCCCCCCCCNC(N)=O GJNDMSSZEBNLPU-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 239000008188 pellet Substances 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
- 150000002978 peroxides Chemical class 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000002530 phenolic antioxidant Substances 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 230000036211 photosensitivity Effects 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical class OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- DOIRQSBPFJWKBE-UHFFFAOYSA-N phthalic acid di-n-butyl ester Natural products CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 229920005668 polycarbonate resin Polymers 0.000 description 1
- 239000004431 polycarbonate resin Substances 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920000306 polymethylpentene Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920005633 polypropylene homopolymer resin Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 229920001290 polyvinyl ester Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 238000009824 pressure lamination Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- PDEFQWNXOUGDJR-UHFFFAOYSA-M sodium;2,2-dichloropropanoate Chemical compound [Na+].CC(Cl)(Cl)C([O-])=O PDEFQWNXOUGDJR-UHFFFAOYSA-M 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- MZHULIWXRDLGRR-UHFFFAOYSA-N tridecyl 3-(3-oxo-3-tridecoxypropyl)sulfanylpropanoate Chemical compound CCCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCCC MZHULIWXRDLGRR-UHFFFAOYSA-N 0.000 description 1
- 238000009966 trimming Methods 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 238000004073 vulcanization Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 235000014692 zinc oxide Nutrition 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/78—Thermal treatment of the extrusion moulding material or of preformed parts or layers, e.g. by heating or cooling
- B29C48/86—Thermal treatment of the extrusion moulding material or of preformed parts or layers, e.g. by heating or cooling at the nozzle zone
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/03—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
- B29C48/07—Flat, e.g. panels
- B29C48/08—Flat, e.g. panels flexible, e.g. films
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/03—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
- B29C48/09—Articles with cross-sections having partially or fully enclosed cavities, e.g. pipes or channels
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/03—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
- B29C48/09—Articles with cross-sections having partially or fully enclosed cavities, e.g. pipes or channels
- B29C48/10—Articles with cross-sections having partially or fully enclosed cavities, e.g. pipes or channels flexible, e.g. blown foils
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/14—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the particular extruding conditions, e.g. in a modified atmosphere or by using vibration
- B29C48/147—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the particular extruding conditions, e.g. in a modified atmosphere or by using vibration after the die nozzle
- B29C48/1472—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the particular extruding conditions, e.g. in a modified atmosphere or by using vibration after the die nozzle at the die nozzle exit zone
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/16—Articles comprising two or more components, e.g. co-extruded layers
- B29C48/18—Articles comprising two or more components, e.g. co-extruded layers the components being layers
- B29C48/21—Articles comprising two or more components, e.g. co-extruded layers the components being layers the layers being joined at their surfaces
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/30—Extrusion nozzles or dies
- B29C48/32—Extrusion nozzles or dies with annular openings, e.g. for forming tubular articles
- B29C48/335—Multiple annular extrusion nozzles in coaxial arrangement, e.g. for making multi-layered tubular articles
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/78—Thermal treatment of the extrusion moulding material or of preformed parts or layers, e.g. by heating or cooling
- B29C48/86—Thermal treatment of the extrusion moulding material or of preformed parts or layers, e.g. by heating or cooling at the nozzle zone
- B29C48/865—Heating
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2791/00—Shaping characteristics in general
- B29C2791/004—Shaping under special conditions
- B29C2791/007—Using fluid under pressure
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Extrusion Moulding Of Plastics Or The Like (AREA)
- Shaping By String And By Release Of Stress In Plastics And The Like (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野]
本発明は、熱可塑性樹脂のインフレーションフィルム成
形方法で得られる多層積層フィルムとその製造方法に関
するものである。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a multilayer laminated film obtained by a thermoplastic resin blown film molding method and a method for producing the same.
[従来の技術]
一般に、先端技術製品、例えば写真感光材料の包装材料
は、光を完全に遮断することの他、ガスバリヤ性、防湿
性、物理強度(破断強度、引裂き強度、衝撃穴あけ強度
、ゲルボテスト強度、摩耗強度等)、ヒートシール適性
(ヒートシール強度、ホットタック性、夾雑物シール性
等)、帯電防止性、平面性等の緒特性を満足することが
要求される。これらの緒特性を単一のフィルム材料で兼
ね具えることは非常に困難であり、従来、複数層からな
る包装材料が用いられていた。[Prior Art] In general, packaging materials for cutting-edge technology products, such as photosensitive materials, not only completely block light, but also have gas barrier properties, moisture proof properties, physical strength (breaking strength, tear strength, impact puncture strength, gelbo test). It is required to satisfy the following properties: strength, abrasion strength, etc.), heat sealability (heat seal strength, hot tack property, contaminant sealing property, etc.), antistatic property, flatness, etc. It is extremely difficult to combine these characteristics with a single film material, and conventionally, packaging materials consisting of multiple layers have been used.
本発明者らも、包装材料の物理強度を向上させるために
、2層の一軸分子配向熱可塑性樹脂フィルムを分子配向
軸が交差するように積層しく特開昭57−6754号)
、又は中間に発泡シート体を挟んで積層した(特開昭5
9−201848号)クロスラミネートフィルムを提案
した。In order to improve the physical strength of packaging materials, the present inventors also developed a method of laminating two layers of uniaxially oriented thermoplastic resin films so that their molecular orientation axes intersect (Japanese Patent Application Laid-Open No. 57-6754).
, or laminated with a foam sheet sandwiched between them (Japanese Patent Application Laid-open No.
No. 9-201848) proposed a cross-laminated film.
また、これら包装材料を品質、コストの点でさらに改良
すべく鋭意研究を行い、多層共押出しインフレーション
フィルムの最内層を特殊な樹脂組成にすることにより、
従来インフレーションフィルム製造の重大故障と考えら
れていたブロッキング現象を利用し、最内層同士をブロ
ッキングさせて接着した物理強度が優れ、安価な多層積
層フィルムからなる包装材料を特願昭62−17730
3号、特願昭62−268227号、特願昭62−29
1947号、特願昭63−1180号、特願昭63−3
390号、特願昭63−6063号で提案した。In addition, we have conducted intensive research to further improve these packaging materials in terms of quality and cost, and by making the innermost layer of the multilayer coextruded blown film a special resin composition,
Utilizing the blocking phenomenon, which was conventionally considered to be a serious failure in the production of blown film, a patent application was filed in 17730/1989 for a packaging material made of an inexpensive multilayer laminated film with excellent physical strength, in which the innermost layers are blocked and bonded together.
No. 3, Patent Application No. 1982-268227, Patent Application No. 1982-29
No. 1947, Patent Application No. 1980-1180, Patent Application No. 1983-3
No. 390 and Japanese Patent Application No. 63-6063.
しかしながら、従来の共押出しTダイフィルムやインフ
レーションフィルムを、接着剤層を介して多層構成とし
た積層フィルムは、トリミングロスが大きく非経済的で
あるだけでなく柔軟性が失なわれ、破袋強度が低下し、
引裂き強度等も低下し、かつカーリングも大きくなる問
題点があった。However, laminated films made of conventional coextruded T-die films and blown films with a multilayer structure with adhesive layers in between are not only uneconomical due to large trimming losses, but also lose flexibility and have poor bag tear strength. decreases,
There were problems in that the tear strength etc. also decreased and curling increased.
また、クロスラミネートフィルムは破袋強度等は優れて
いるが高価であり、かつ接着剤層で各層が完全に接着さ
れると硬くなったり、引裂き強度等が低下したり、カー
ルが大きくなったりし、種種のトラブルが発生しやすか
った。In addition, although cross-laminated films have excellent bag tear strength, they are expensive, and when each layer is completely bonded with an adhesive layer, they become hard, have reduced tear strength, and become curly. , a variety of problems were likely to occur.
一方、特願昭62−177303号等で開示したインフ
レーションフィルムの最内層同士をブロッキングにより
接着した積層フィルムは、接着剤層も積層工程も必要と
せず、従来のインフレーションフィルムのように両端を
切断してシートフィルムとする必要がないため耳ロスの
発生が無く、単位面積当りの積層フィルムコストを大巾
に低下させ、かつ物理強度を大巾に向上できる優れた包
装材料である。しかし、この積層フィルムを用いて他の
フレキシブルシートと積層しようとする時には、積層フ
ィルムの最内側同士をブロッキングにより接着させる面
積が95%以上になるようにしないと、未接着部分の空
気によりラミネート工程でシワやブロッキング部の剥離
が発生しロスが多発する。On the other hand, the laminated film disclosed in Japanese Patent Application No. 177303/1983, in which the innermost layers of blown films are bonded together by blocking, does not require an adhesive layer or a lamination process, and can be cut at both ends like conventional blown films. It is an excellent packaging material that eliminates the need to form a sheet film, eliminates the occurrence of edge loss, greatly reduces the cost of laminated film per unit area, and greatly improves physical strength. However, when trying to laminate other flexible sheets using this laminated film, the area where the innermost sides of the laminated film are adhered to each other by blocking must be 95% or more, otherwise the lamination process will be affected by the air in the unbonded parts. Wrinkles and peeling of the blocking part occur, resulting in frequent losses.
また、最内層同士のブロッキングによる接着強度が、冷
却条件やインフレーションフィルム成形時の室内の温湿
度により変動し易いうえ、多層共押出しインフレーショ
ンフィルムの最内層の樹脂組成が限定された。また、最
内層と最外層の樹脂組成をほぼ同じにした場合は、最内
層同士のブロッキングだけでなく、冷却して巻き取られ
た時に両表面に位置する最外層同士がブロッキングして
積層フィルムとして使用できなくなったり、最外層同士
をブロッキングしないように配慮すると、接着させよう
とする最内層同士もブロッキングしなくなるなどの問題
があった。Furthermore, the adhesive strength due to blocking between the innermost layers tends to fluctuate depending on the cooling conditions and the indoor temperature and humidity during molding of the blown film, and the resin composition of the innermost layer of the multilayer coextruded blown film is limited. In addition, if the resin composition of the innermost layer and the outermost layer is almost the same, not only the innermost layers will block each other, but also the outermost layers on both surfaces will block each other when cooled and rolled up, resulting in a laminated film. If care is taken to prevent the outermost layers from blocking each other, there are problems such as the innermost layers to be bonded also not blocking each other.
本発明は、以上の問題点を解決し、ブロッキングによる
積層フィルムにおける物理強度や破袋強度が大きく、柔
軟で、カールが小さく、多層共押出しインフレーション
フィルムだけでなく単層インフレーションフィルムでも
最内側同士のブロッキングによ、る接着面積や接着強度
を任意にコントロール可能で、インフレーションフィル
ム成形時の冷却条件や室内の温湿度、最内側の樹脂組成
による影舌を受けることが少ない、安価で品質の優れた
積層フィルムとその製造方法を提供することを目的とす
る。The present invention solves the above problems, has high physical strength and bag breakage strength in a laminated film by blocking, is flexible, has little curling, and can be used not only for multilayer coextruded blown films but also for single-layer blown films. By blocking, the adhesive area and adhesive strength can be controlled arbitrarily, and it is less affected by the cooling conditions during blown film molding, indoor temperature and humidity, and the innermost resin composition, and is inexpensive and of excellent quality. The purpose of the present invention is to provide a laminated film and a method for manufacturing the same.
本発明は上記目的を達成するためになされたもので、積
層フィルムは、ブロッキングにより接着されている樹脂
が、環状ダイスのグイリップから押し出される際にダイ
リップ内側近傍に設けられた局部加熱環状ヒータで加熱
されていることを特徴として構成されている。The present invention has been made to achieve the above object, and the laminated film is heated by a locally heated annular heater installed near the inside of the die lip when the resin bonded by blocking is extruded from the gui lip of the annular die. It is structured with the following characteristics:
また、積層フィルムの製造方法は、環状ダイスのダイリ
ップの内側近傍に設けた局部加熱環状ヒータで、最内側
の樹脂の表面温度を最外側の樹脂の表面温度より高くな
るように加熱しつつグイリップから樹脂を押し出し、そ
の後最内側同士をブロッキングにより接着させることを
特徴として構成されている。In addition, the laminated film manufacturing method uses a locally heated annular heater installed near the inside of the die lip of the annular die to heat the innermost resin surface temperature to be higher than the outermost resin surface temperature from the die lip. The feature is that the resin is extruded and then the innermost parts are bonded together by blocking.
局部加熱環状ヒータの埋め込み位置は、ダイリップ部の
材質、強度や環状ヒータ容量により決定されるが通常は
グイリップから2〜50mm、好ましくは3〜20mm
の距離でダイリップ周囲からほぼ等間隔に設置される。The embedded position of the local heating annular heater is determined by the material and strength of the die lip and the capacity of the annular heater, but is usually 2 to 50 mm from the die lip, preferably 3 to 20 mm.
They are installed at approximately equal intervals from the periphery of the die lip at a distance of .
局部加熱環状ヒータの埋め込みの深さは環状ダイス表面
から50+nm以内の深さが好ましく、これを越えると
局部加熱効果が1れる。The embedded depth of the local heating annular heater is preferably within 50+ nm from the surface of the annular die; if this is exceeded, the local heating effect is reduced.
この局部加熱環状ヒータは、環状ダイスの外部及び必要
に応じ内部に設けた一般的な樹脂加熱手段と併用される
。環状ダイスから吐出された円筒状フィルムの最外側を
冷却固化するには従来の公知の空冷や水冷等の方法がと
られる。This local heating annular heater is used in combination with general resin heating means provided outside and, if necessary, inside the annular die. In order to cool and solidify the outermost part of the cylindrical film discharged from the annular die, conventionally known methods such as air cooling or water cooling are used.
ブロッキングを強固にしたり、さらに溶着によりさらに
強固に積層するためには、絹目状、格子状、平行筋状(
タテ又はヨコ)斜め筋状等種々の形状の加圧式のエンボ
スロールや加熱ロール等により押圧積層してもよい。In order to strengthen the blocking or to further strengthen the lamination by welding, it is necessary to
Pressure lamination may be performed using a pressurized embossing roll, heating roll, etc. in various shapes such as vertical or horizontal) diagonal stripes.
これらのエンボスロールや加熱ロール等はインフレーシ
ョンフィルム成形機のスクイズロールにツブロール)の
前後のインフレーションフィルム成形工程中(オンライ
ン)にもうけてもオフラインで加工してもよい。These embossing rolls, heating rolls, etc. may be used during the blown film forming process (online) before or after the squeeze roll or tube roll of the blown film forming machine, or may be processed offline.
そして局部加熱環状ヒータの温度コントロールにより、
希望するブロッキング接着強度、ブロッキング接着面積
の積層フィルムを得ることができる。And by controlling the temperature of the local heating annular heater,
A laminated film with desired blocking adhesive strength and blocking adhesive area can be obtained.
本発明の積層フィルムに用いることが可能な樹脂として
は、例えば、高圧法分岐状低密度ポリエチレン(以後L
DPEと表示)樹脂、直鎖状低密度ポリエチレン(エチ
レン−αオレフイン共重合体樹脂、以後L−LDPEと
表示)樹脂、中・低圧法中密度ポリエチレン樹脂、中・
低圧法高密度ポリエチレン(以後HDPEと表示)樹脂
、超低密度L −L D P E樹脂、ホモポリプロピ
レン樹脂、プロピレン・エチレンランダム共重合体樹脂
、プロピレン・エチレンブロック共重合体樹脂、ポリブ
テン−1樹脂、ポリ4メチルペンテン−1樹脂、ポリイ
ソブチレン樹脂、エチレン−酢酸ビニル樹脂、エチレン
−アクリル酸エチル樹脂、エチレン−メタクリル酸エチ
ル樹脂、エチレン−アクリル酸樹脂、アイオノマー樹脂
、変性エチレン樹脂、変性エチレン共重合体樹脂、変性
プロピレン樹脂、エラストマー樹脂、各種ポリエステル
樹脂(ポリエチレンテレフタレート樹脂、ポリエチレン
イソフタレート樹脂等)、各種ポリアミド樹脂(ナイロ
ン6樹脂、ナイロン66樹脂、ナイロン11樹脂、ナイ
ロン12樹脂等)、ポリスチレン樹脂、塩素化ポリエチ
レン樹脂等が挙げられる。これらの樹脂は単独あるいは
ブレンドして用いることができる。Examples of resins that can be used in the laminated film of the present invention include high-pressure branched low-density polyethylene (hereinafter referred to as L
DPE) resin, linear low density polyethylene (ethylene-α olefin copolymer resin, hereinafter referred to as L-LDPE) resin, medium/low pressure medium density polyethylene resin, medium/low pressure process medium density polyethylene resin,
Low pressure high density polyethylene (hereinafter referred to as HDPE) resin, ultra low density L-LDPE resin, homopolypropylene resin, propylene/ethylene random copolymer resin, propylene/ethylene block copolymer resin, polybutene-1 resin , poly(4-methylpentene-1) resin, polyisobutylene resin, ethylene-vinyl acetate resin, ethylene-ethyl acrylate resin, ethylene-ethyl methacrylate resin, ethylene-acrylic acid resin, ionomer resin, modified ethylene resin, modified ethylene copolymer Combined resin, modified propylene resin, elastomer resin, various polyester resins (polyethylene terephthalate resin, polyethylene isophthalate resin, etc.), various polyamide resins (nylon 6 resin, nylon 66 resin, nylon 11 resin, nylon 12 resin, etc.), polystyrene resin, Examples include chlorinated polyethylene resin. These resins can be used alone or in a blend.
特に好ましいものはL−LDPE系樹脂であり、単層の
インフレーションフィルムまたはL−LDPE系樹脂を
最内側、他の熱可塑性樹脂とエチレン共重合体樹脂を1
0重量%混練した樹脂を最外側の組合せとする多層共押
出しインフレーションフィルムの積層フィルムとして好
適である。Particularly preferred is L-LDPE resin, with a single-layer blown film or L-LDPE resin placed on the innermost layer, and other thermoplastic resins and ethylene copolymer resin placed on the innermost layer.
It is suitable as a laminated film of a multilayer coextruded blown film having 0% by weight of kneaded resin as the outermost combination.
この場合、このL−LDPE系樹脂は、密度が0.92
5g/cJ以下であることが好ましい。密度が0.92
5g/cfflを越えると、フィルム成形時の温度を上
げてもブロッキングにより接着力が弱く層間剥離を起こ
しやすい。また、L−LDPE系樹脂は、L−LDPE
樹脂を20重重景以上含み、好ましくはL−LDPE樹
脂50重量%以上含むものであり、軟化点は110°C
以下であることが好ましい。In this case, this L-LDPE resin has a density of 0.92
It is preferably 5 g/cJ or less. Density is 0.92
If it exceeds 5 g/cffl, even if the temperature during film molding is raised, the adhesive force will be weak due to blocking and delamination will easily occur. In addition, the L-LDPE resin is L-LDPE
It contains at least 20% of resin, preferably at least 50% by weight of L-LDPE resin, and has a softening point of 110°C.
It is preferable that it is below.
また、エチレンアクリル酸エステル系樹脂も好ましく、
メチルアクリレート及び/又はエチルアクリレート含量
が7重量%以上のエチレンアクリル酸エステル樹脂を5
0重量%以上含むエチレンアクリル酸エステル系樹脂と
、エチレン共重合体樹脂を10重量%以上含む熱可塑性
樹脂との組み合わせも良い。Moreover, ethylene acrylic acid ester resin is also preferable,
5% of ethylene acrylate resin with a methyl acrylate and/or ethyl acrylate content of 7% by weight or more
A combination of an ethylene acrylate resin containing 0% by weight or more and a thermoplastic resin containing 10% by weight or more of an ethylene copolymer resin is also good.
同じくエチレン酢酸ビニル共重合体樹脂も好ましく、更
に詳しくは、醋酸ビニル含量が5重量%以上のエチレン
醋酸ビニル系共重合体樹脂と、エチレン共重合体樹脂を
10重量%以上含む熱可塑性樹脂との組み合わせも良い
。Similarly, ethylene vinyl acetate copolymer resin is also preferable, and more specifically, an ethylene vinyl acetate copolymer resin having a vinyl acetate content of 5% by weight or more and a thermoplastic resin containing ethylene copolymer resin 10% by weight or more. Good combination too.
外側に使用される熱可塑性樹脂は、前記最内側に用いら
れる樹脂などのほか、ポリ塩化ビニリデン樹脂、ポリ塩
化ビニル樹脂、ポリカーボネート樹脂などの公知の樹脂
及びそれらの変性樹脂が用いられる。ヒートシール適性
向上に点からL−LDPE樹脂、EVA樹脂、EEA樹
脂、EMA樹脂、アイオノマー樹脂、EAA樹脂等にエ
チレン共重合体樹脂を10重量%以上含むことが好まし
い。As the thermoplastic resin used on the outside, in addition to the resin used on the innermost side, known resins such as polyvinylidene chloride resin, polyvinyl chloride resin, polycarbonate resin, and modified resins thereof are used. From the viewpoint of improving heat-sealability, it is preferable that the L-LDPE resin, EVA resin, EEA resin, EMA resin, ionomer resin, EAA resin, etc. contain 10% by weight or more of ethylene copolymer resin.
本発明の積層フィルムにおいては、必要によりフィルム
の各層に遮光性物質や滑剤、酸化防止剤、ブロッキング
防止剤およびその他の添加剤を用いることができる。In the laminated film of the present invention, a light-shielding substance, a lubricant, an antioxidant, an antiblocking agent, and other additives can be used in each layer of the film, if necessary.
本発明に使用可能な遮光物質としては、各種カーボンブ
ランク、酸化鉄、亜鉛華、酸化チタン、窒化チタン、ク
レー、アルミニウム粉末、アルミニウムペースト、炭酸
カルシウム、マイカ、硫酸バリウム、タルクζカドミウ
ム系顔料、弁柄、コバルトブルー、銅フタロシアニン系
顔料、モノアゾ又はポリアゾ系顔料、アニリンブラック
等の有機系顔料や無機系顔料等が挙げられる。Examples of light-shielding substances that can be used in the present invention include various carbon blanks, iron oxide, zinc white, titanium oxide, titanium nitride, clay, aluminum powder, aluminum paste, calcium carbonate, mica, barium sulfate, talc ζ cadmium pigments, and valves. Examples include organic pigments and inorganic pigments such as pattern, cobalt blue, copper phthalocyanine pigments, monoazo or polyazo pigments, and aniline black.
これらの遮光物質の中では、品質、コスト、遮光能力等
の点で、光を吸収または反射しやすい着色顔料特に黒色
顔料の各種カーボンブラック及び窒化チタンや光反射性
遮光性物質のアルミニウム粉末及びアルミニウムペース
トより低揮発物質を除去したものが好ましい。Among these light-shielding substances, colored pigments that easily absorb or reflect light, especially black pigments such as various carbon blacks and titanium nitride, and light-reflecting light-shielding substances such as aluminum powder and aluminum It is preferable to use a paste with lower volatile substances removed than a paste.
これらの遮光物質を各層に配合する方法としては従来か
らよく行われているマスターバッチ着色法やコンパウン
ド着色法等がある。上記遮光物質は使用樹脂、使用機械
、コスト等により使用形態として粉末状着色剤、ペース
ト状着色剤、潤性着色剤、マスターバッチ、染顔料、カ
ラードベレット等がある。Methods for blending these light-shielding substances into each layer include masterbatch coloring, compound coloring, and the like, which have been commonly used in the past. The above-mentioned light-shielding substances may be used in various forms, such as powder colorants, paste colorants, moisturizing colorants, masterbatches, dyes and pigments, and colored pellets, depending on the resin used, the machine used, the cost, etc.
特に遮光性の確保、コスト及び物理強度が向上する点で
カーボンブラックが好ましい。Carbon black is particularly preferred because it ensures light-shielding properties and improves cost and physical strength.
カーボンブラックは原料によりガスブラック、ファーネ
スブラック、チャンネルブラック、アントラセンブラッ
ク、アセチレンブラック、油煙、粉煙、アニリンブラッ
ク、ベジタブルブラック等に分類される。Carbon black is classified into gas black, furnace black, channel black, anthracene black, acetylene black, oil smoke, powder smoke, aniline black, vegetable black, etc. depending on the raw material.
これらのカーボンブラックの中では、pH5〜9、特に
pH6〜8、平均粒子径10〜1201nμのものが好
ましく、特にpH6〜9、平均粒子径15〜50mμの
アセチレンカーボンブラック又はファーネスカーボンブ
ラックが好ましい。このようなpJI及び粒子径のもの
を使用することによって写真感光材料のカプリの発生が
少なく、感光度の増減の発生が少なく、遮光能力が大き
く、ブッ、フィッシヱアイ及びピンホールが発生しにく
い等の数々の利点を有する包装材料を製造できる。Among these carbon blacks, those having a pH of 5 to 9, particularly pH 6 to 8, and an average particle size of 10 to 1201 nμ are preferable, and acetylene carbon black or furnace carbon black with a pH of 6 to 9 and an average particle size of 15 to 50 mμ are particularly preferable. By using such pJI and particle size, the photosensitive material has less capri, less increase and decrease in photosensitivity, has a large light shielding ability, and is less likely to produce bubbles, fish eyes, and pinholes. Packaging materials can be produced that have a number of advantages.
本発明の積層フィルムでは遮光性、コスト、物性向上の
目的からファーネスカーボンブラックが好ましく、高価
ではあるが帯電防止効果を有するアセチレンカーボンブ
ラック、ケッチエンカーボンブラックも好ましい。カー
ボンブランクの含有量は0.05〜15.0重量%が好
ましい。In the laminated film of the present invention, furnace carbon black is preferable for the purpose of improving light-shielding properties, cost, and physical properties, and acetylene carbon black and ketchiene carbon black, which are expensive but have an antistatic effect, are also preferable. The content of carbon blank is preferably 0.05 to 15.0% by weight.
0.05重盟%未満では遮光性を確保するためにはさら
に他の遮光層を積層する必要がある。15.0重量%を
こえるとフィルムの物理強度やヒートシール性が低下し
、コストアップになる。If it is less than 0.05% by weight, it is necessary to further laminate another light-shielding layer in order to ensure light-shielding properties. If it exceeds 15.0% by weight, the physical strength and heat sealability of the film will decrease, leading to an increase in cost.
滑剤は、主として樹脂の流動性等を良くし製品挿入性、
ハンドリング性、フィルム成形加工性を向上させるため
のものである。さらにハクリ帯電防止性を有することが
判明した。この滑剤の含有量は0.01〜5.0重量%
が好ましい。The lubricant mainly improves the fluidity of the resin and improves the ease of product insertion.
This is to improve handling properties and film forming processability. Furthermore, it was found to have antistatic properties against peeling. The content of this lubricant is 0.01 to 5.0% by weight
is preferred.
0.01重量%未満では一ト記特性を向上させる効果が
ほとんどなく混練経費増となるだけである。If it is less than 0.01% by weight, there will be little effect of improving the above-mentioned properties and the kneading cost will only increase.
5.0重量%をこえると押出し機のスクリューとのスリ
ップ発生が多くなり均一の厚さのフィルムを成形するこ
とが困難になる。If it exceeds 5.0% by weight, slippage with the extruder screw will increase, making it difficult to form a film of uniform thickness.
さらにブリードアウトしやすくなり写真感光材料用に用
いた場合は感光層に付着して現像阻害等の故障が発生す
る。Furthermore, they tend to bleed out, and when used in photographic materials, they adhere to the photosensitive layer and cause problems such as development inhibition.
代表的滑剤としては、パラフィンワックス、や金属石鹸
などのほか、
(1)シリコーン系滑剤、
(2)オレイン酸アミド系滑剤、
(3)エルカ酸アミド系滑剤、
(4)ステアリン酸アミド系滑剤、
(5)ビス脂肪酸アミド系滑剤、
(6)アルキルアミン系滑剤;エレクトロストリッパー
TS−2(花王石鹸)等がある。Typical lubricants include paraffin wax, metal soap, etc., as well as (1) silicone-based lubricants, (2) oleic acid amide-based lubricants, (3) erucic acid amide-based lubricants, (4) stearic acid amide-based lubricants, (5) Bis fatty acid amide lubricant, (6) Alkylamine lubricant; Electro Stripper TS-2 (Kao Soap), etc.
なお、ジメチルポリシロキサンは粘度が1,000〜1
00.0OOCPS (25°C測定)であることが好
ましい。Note that dimethylpolysiloxane has a viscosity of 1,000 to 1
00.0OOCPS (measured at 25°C) is preferable.
1.0OOCPS未満では写真感光材料に悪影響を与え
る(カプリや感光度変動を発生させる。)。If it is less than 1.0OOCPS, it will have an adverse effect on the photographic light-sensitive material (causing capri and sensitivity fluctuations).
100、000(1:PSをこえると取扱い性が悪く、
且つ非常に高価になり実用化が困難となるからである。If it exceeds 100,000 (1:PS), it becomes difficult to handle.
Moreover, it is very expensive and difficult to put into practical use.
酸化防止剤の代表的例を次に示す。Typical examples of antioxidants are shown below.
フェノール系
n−オクタデシル−3(3’、5’−ジーL−ブチル4
′ヒドロキシフェニル)プロピネート、2,6ジーt−
ブチル4−メチルフェノール、2.6ジーL−ブチル−
p−クレゾール、2,2゛−メチレンビス(4−メチル
−6−t−ブチルフェノール)、4,4゛−チオビス(
3−メチル6−t−ブチルフェノール)、4,4゛−ブ
チリデンビス(3−メチル−6−を−ブチルフェノール
)、ステアリル−β(3,5−ジ4−ブチル4−ヒドロ
キシフェニル)プロピオネート、1,1.3−トリス(
2−メチル−4−ヒドロキシ−5−t−ブチルフェニル
)ブタン、11315−トリメチル−2,4,6−)リ
ス(3,5−ジーも=ブチル−4−ヒドロキシベンジル
)ベンゼン、オクタデシル−3−(3,5−ジ−t−ブ
チル−4ヒドロキシフエニル)プロピオネート、テトラ
キス〔メチレン−3(3’、5’−ジ−t−ブチル−4
゛−ヒドロキシフェニル)プロピオネートコメタン等、
硫黄系
ジラウリル−3,3“−チオジプロピオネート、シミリ
スチル−3,3゛−チオジプロピオネート、ラウリルス
テアリルチオジプロピオネート、ジステアリル−3゛−
チオジプロピオネート、ジトリデシル−3,3’−チオ
ジプロピオネート等
燐系
トリノニルフェニルフォスファイト、トリフェニルフォ
スファイト等がある。Phenolic n-octadecyl-3(3',5'-di-L-butyl4
'Hydroxyphenyl)propinate, 2,6 di-t-
Butyl 4-methylphenol, 2.6-di-L-butyl-
p-cresol, 2,2゛-methylenebis(4-methyl-6-t-butylphenol), 4,4゛-thiobis(
3-methyl-6-tert-butylphenol), 4,4'-butylidenebis(3-methyl-6-butylphenol), stearyl-β(3,5-di4-butyl-4-hydroxyphenyl)propionate, 1,1 .3-Tris (
2-Methyl-4-hydroxy-5-t-butylphenyl)butane, 11315-trimethyl-2,4,6-)lis(3,5-di-butyl-4-hydroxybenzyl)benzene, octadecyl-3- (3,5-di-t-butyl-4hydroxyphenyl)propionate, tetrakis[methylene-3(3',5'-di-t-butyl-4
(Hydroxyphenyl)propionate comethane, etc.
Sulfur-based dilauryl-3,3"-thiodipropionate, similystyl-3,3"-thiodipropionate, laurylstearylthiodipropionate, distearyl-3"-
Examples include thiodipropionate, ditridecyl-3,3'-thiodipropionate, phosphorus trinonylphenyl phosphite, triphenyl phosphite, and the like.
特に2.6−ジーt−ブチル−p−クレゾール(BHT
)や低連発性の高分子量フェノール型酸化防止剤(商品
名1reganox 1010+ Ireganox
1076+Topano ICA等)やジラウリルチオ
ジプロピオネートやジステアリルチオジプロピオネート
やシアルキスフォスフェート等の1つ以上、特に2つ以
上を併用するのが効果的である。In particular, 2,6-di-t-butyl-p-cresol (BHT)
) and low-recurrence high molecular weight phenolic antioxidants (product name 1reganox 1010+ Ireganox
1076+Topano ICA, etc.), dilauryl thiodipropionate, distearyl thiodipropionate, sialkis phosphate, etc. It is effective to use one or more, especially two or more of them in combination.
酸化防止剤は0.01〜2.00重量%用いることが好
ましい。酸化防止剤が0.01重量%未満であると、樹
脂の酸化防止効果が小さくなり、樹脂焼けにより塊(ブ
ッ)の発生が多(なって、外観が悪くなる。又このブツ
の発生は写真感光材料を包装した際に圧力かぶり等の発
生の原因ともなる。It is preferable to use 0.01 to 2.00% by weight of the antioxidant. If the antioxidant content is less than 0.01% by weight, the antioxidant effect of the resin will be reduced, and the appearance will be poor due to the occurrence of lumps due to resin burning. It also causes pressure build-up when packaging photosensitive materials.
また、2.00重量%を越えると、酸化・還元作用を利
用している写真感光材料に悪影響を及ぼすだけでなく経
時でブリードアウトして外観が悪くなる。Moreover, if it exceeds 2.00% by weight, it not only has an adverse effect on photographic materials that utilize oxidation and reduction effects, but also bleeds out over time, resulting in poor appearance.
ブロッキング防止剤の代表例を次に示す。Representative examples of antiblocking agents are shown below.
酸化珪素(シリカ)、カルシウムシリケート、ケイ酸ア
ルミニウム、炭酸カルシウム、タルク(ケイ酸マグネシ
ウム)、高級脂肪酸ポリビニルエステル、n−オクタデ
シルウレア、ジカルボン酸エステルアミド、N、N’−
ジオレイルオキサアミド、N−エタノールステアリン酸
アミド等。Silicon oxide (silica), calcium silicate, aluminum silicate, calcium carbonate, talc (magnesium silicate), higher fatty acid polyvinyl ester, n-octadecyl urea, dicarboxylic acid ester amide, N, N'-
Dioleyl oxamide, N-ethanol stearic acid amide, etc.
ブロッキング防止剤の他でブロッキング防止効果を有す
る物としては各種滑剤、各種界面活性剤、密度0.93
5g/cn!以上のポリエチレン樹脂等がある。In addition to anti-blocking agents, substances that have an anti-blocking effect include various lubricants, various surfactants, and density 0.93.
5g/cn! There are the above polyethylene resins, etc.
添加剤の代表例を以下に記載するが、本発明はこれに限
定されるものではなく、公知のあらゆるものの中から選
択できる。Representative examples of additives are described below, but the present invention is not limited thereto, and any known additives can be selected.
(添加剤種類) (代 表 例)(1)可塑剤
;フタル酸エステル、グリコールエステル、脂肪酸
エステル、リ
ン酸エステル等
(2)安定剤 ;鉛系、カドミウム系、亜鉛系、アル
カリ土類金属系、有機スズ
系等
(3)帯電防止剤;陽イオン系界面活性剤、陰イオン系
界面活性剤、非イオン系界
部活性剤、両面活性剤、各種カ
ーボンブラック、金属粉末、グ
ラファイト等
;燐酸エステル、ハロゲン化燐酸
エステル、ハロゲン(IJI、無a
物、含燐ポリオール等
;アルミナ、カオリン、クレー
炭酸カルシウム、マイカ、タル
ク、酸化チタン、硫酸バリウム、
シリカ等
;ガラスロービング、金属繊維、
ガラス繊維、ガラスミルドファ
イバー、炭素繊維等
;無機発泡剤(炭酸アンモニア、
重炭酸ソーダ)、有機発泡剤
にトロソ系、アゾ系)、等
(8)加硫剤 ;加硫促進剤、促進助剤等(9)劣化
防止剤;紫外線吸収剤、酸化防止剤、金属不活性化剤、
過酸化物分解剤
(6)補強剤
(7)発泡剤
(5)充填剤
(4)難燃剤
(10)カップリング剤;シラン系、チタネート系、ク
ロム系、アルミニウム系等
である。(Additive types) (Representative examples) (1) Plasticizers: Phthalate esters, glycol esters, fatty acid esters, phosphate esters, etc. (2) Stabilizers: Lead-based, cadmium-based, zinc-based, alkaline earth metal-based , organic tin-based, etc. (3) Antistatic agents; cationic surfactants, anionic surfactants, nonionic surfactants, bifacial active agents, various carbon blacks, metal powders, graphite, etc.; phosphate esters , halogenated phosphate esters, halogens (IJI, aluminium-free, phosphorus-containing polyols, etc.); alumina, kaolin, clay calcium carbonate, mica, talc, titanium oxide, barium sulfate, silica, etc.; glass roving, metal fibers, glass fibers, glass Milled fibers, carbon fibers, etc.; inorganic blowing agents (ammonia carbonate, sodium bicarbonate), organic blowing agents (toroso-based, azo-based), etc. (8) Vulcanizing agents; vulcanization accelerators, accelerators, etc. (9) Deterioration prevention Agent; UV absorber, antioxidant, metal deactivator,
Peroxide decomposer (6) Reinforcing agent (7) Foaming agent (5) Filler (4) Flame retardant (10) Coupling agent; Silane-based, titanate-based, chromium-based, aluminum-based, etc.
本発明の積層フィルムは、最内側同士をブロッキングに
より接着させた多層積層フィルムそのまま、又は接着剤
層を介し、又は接着剤層を介さずに各種のフレキシブル
シートを積層した多層積層フィルムとして用いることも
できる。The laminated film of the present invention can be used as a multilayer laminated film in which the innermost sides are bonded together by blocking, or as a multilayer laminated film in which various flexible sheets are laminated with or without an adhesive layer. can.
本発明の積層フィルムは各種製品の包装等に用いられる
が、写真感光材料、食料品、医薬品、化学物質等の感光
物質の包装に好適である。The laminated film of the present invention is used for packaging various products, and is suitable for packaging photosensitive materials such as photographic materials, foodstuffs, pharmaceuticals, and chemical substances.
特に、わずかなガスや光や湿度により品質が破壊される
ハロゲン化銀写真感光材料、ジアゾ写真感光材料、感光
性樹脂写真感光材料、自己現像型写真感光材料、拡散転
写型写真感光材料、感熱写真感光材料、光定着型感熱写
真感光材料、転写型熱現像感光材料、直接ポジ型感光材
料、紫外線硬化型感光材料等に好適である。In particular, silver halide photographic materials, diazo photographic materials, photosensitive resin photographic materials, self-developing photographic materials, diffusion transfer photographic materials, and thermosensitive materials whose quality is destroyed by slight gases, light, and humidity. It is suitable for photosensitive materials, photofixing type thermographic photosensitive materials, transfer type heat developable photosensitive materials, direct positive type photosensitive materials, ultraviolet curing type photosensitive materials, etc.
本発明の積層フィルムを上記の写真感光材料に適用する
場合には、−重平袋、二重平袋、自立袋、−重ガゼット
袋、二重ガゼツト袋、積層フィルム、防湿遮光箱の内貼
り、明室装填遮光マガジンの内貼り又は内装袋、リーダ
ー紙等公知のあらゆる形態のものに使用可能である。When the laminated film of the present invention is applied to the above-mentioned photographic materials, - double flat bags, double flat bags, self-standing bags, - heavy gusseted bags, double gusseted bags, laminated films, inner lining of moisture-proof and light-shielding boxes, It can be used for all known forms such as inner lining of room-loading light-shielding magazines, inner bags, and leader paper.
製袋に使用する方法は積層フィルムの性質に応じて、ヒ
ートシール、溶断シール、インパルスシール、超音波シ
ール、高周波シールなど、従来公知のプラスチックフィ
ルムのシール法による。なお、適宜の接着剤、粘着剤な
どを使用して製袋することも可能である。The method used for bag making is a conventional plastic film sealing method such as heat sealing, fusing sealing, impulse sealing, ultrasonic sealing, high frequency sealing, etc., depending on the properties of the laminated film. Note that it is also possible to make bags using an appropriate adhesive, adhesive, or the like.
本発明は、環状ダイスのダイリップ内側に局部加熱環状
ヒータを設けて、ダイリップ内側の樹脂を加熱して押し
出しているため、ダイリップ最内側の樹脂の表面温度を
最外側の樹脂の表面温度よりも高いブロッキングし易い
温度に保持する。In the present invention, a local heating annular heater is provided inside the die lip of the annular die to heat and extrude the resin inside the die lip, so that the surface temperature of the resin on the innermost side of the die lip is higher than the surface temperature of the resin on the outermost side. Maintain temperature at which blocking is easy.
従って最内側の樹脂組成の影言や、フィルム成形時の冷
却条件や室内の温湿度等の影響を受けることが少なく、
また、加熱温度の調節により接着面積、接着強度の調節
を行う。Therefore, it is less affected by the effects of the innermost resin composition, cooling conditions during film molding, indoor temperature and humidity, etc.
Furthermore, the adhesive area and adhesive strength are adjusted by adjusting the heating temperature.
また、ダイリップ出口の局所的加熱であるため樹脂の劣
化やメルトフラクチャーを生ずることなくダイリップ部
の樹脂の流動を良好にしている。In addition, since the heating is performed locally at the exit of the die lip, the flow of the resin at the die lip is improved without causing resin deterioration or melt fracture.
以下、本発明の積層フィルムの実施例を第1図から第4
図に基づいて説明する。Examples of the laminated film of the present invention are shown in Figures 1 to 4 below.
This will be explained based on the diagram.
第1図の積層フィルムは、単層インフレーションフィル
ムlがブロッキング部Bで疑似接着された2層で構成さ
れている。The laminated film shown in FIG. 1 is composed of two layers in which a single-layer blown film 1 is pseudo-adhered at a blocking portion B.
第2図の積層フィルムは、内側フィルム層2と外側フィ
ルム層3との2層共押出しフィルム4がブロッキング部
Bで疑似接着されて構成されている。The laminated film shown in FIG. 2 is composed of a two-layer coextruded film 4 consisting of an inner film layer 2 and an outer film layer 3, which are pseudo-adhered at a blocking portion B.
第3図の積層フィルムは内側フィルム層2と外側フィル
ム層3とこれらの間の中間フィルム層5から成る3N共
押出しインフレーションフィルム6がブロッキング部B
で疑似接着されて構成されている。以上単層及び多層共
押出しインフレーションフィルムをブロッキング部で疑
似接着された積層フィルムはいずれもブロッキング部B
を中心として上・下対称の層構成になっていることが特
徴である。The laminated film shown in FIG. 3 is a 3N coextruded blown film 6 consisting of an inner film layer 2, an outer film layer 3, and an intermediate film layer 5 between them.
It is made up of pseudo-adhesive. The above laminated films in which single-layer and multi-layer coextruded blown films are pseudo-adhered in the blocking part are all in the blocking part B.
It is characterized by a layered structure that is symmetrical upward and downward with .
第4図の積層フィルムは、2層共押出しフィルム4がブ
ロッキング部Bで疑似接着された4層積層フィルムに、
接着剤層7を介してフレキシブルシート8が積層されて
構成されている。The laminated film in FIG. 4 is a four-layer laminated film in which a two-layer coextruded film 4 is pseudo-adhered at a blocking part B.
Flexible sheets 8 are laminated with an adhesive layer 7 in between.
次に、以上のような本発明の積層フィルムを製造する方
法の一実施例を第5図から第7図に基づいて説明する。Next, an embodiment of the method for manufacturing the laminated film of the present invention as described above will be described based on FIGS. 5 to 7.
第5図はインフレーションフィルム製造装置の概略図、
第6図は同上環状ダイスの横断面図、第7図は同上環状
ダイスの縦断面図である。Figure 5 is a schematic diagram of the blown film manufacturing equipment;
FIG. 6 is a cross-sectional view of the same annular die, and FIG. 7 is a longitudinal cross-sectional view of the same annular die.
第5図において、符号11は樹脂を加熱混練する押出し
機、符号12はスリット(図示せず)から溶融樹脂をチ
ューブ状に押出す環状ダイス、符号13は圧縮空気を送
り込む送風管、符号14はチューブ状に押し出された溶
融樹脂を冷却するエアーリング、符号15はチューブ状
樹脂フィルム16を案内するガイドローラ、符号7はチ
ューブ状樹脂フィルム16を平板上に案内するガイド板
、複数のパスロールを並べてもよい符号18はチューブ
状樹脂フィルム16を挟んで引き上げる引取用スクイズ
ロールにツブロール)、符号19はフィルムを巻取る巻
取機である。In FIG. 5, reference numeral 11 is an extruder for heating and kneading the resin, reference numeral 12 is an annular die for extruding the molten resin into a tube shape through a slit (not shown), reference numeral 13 is an air pipe for feeding compressed air, and reference numeral 14 is an annular die for extruding the molten resin into a tube shape. An air ring cools the molten resin extruded into a tube, a guide roller 15 guides the tubular resin film 16, a guide plate 7 guides the tubular resin film 16 onto a flat plate, and a plurality of pass rolls are arranged side by side. The reference numeral 18 is a take-up squeeze roll that pinches and pulls up the tubular resin film 16, and the reference numeral 19 is a winder that winds up the film.
前記環状ダイス12は、第6図及び第7図に示すように
、ダイリップ21の内側近傍に同心円状の局部加熱環状
ヒータ22を埋め込まれており、ダイリップ21の内側
を加熱し、グイリップ21から押し出されるフィルムの
最内側の樹脂の表面温度を高めニップロール等の圧縮手
段によるブロッキングを容易にしている。As shown in FIGS. 6 and 7, the annular die 12 has a concentric local heating annular heater 22 embedded near the inside of the die lip 21 to heat the inside of the die lip 21 and extrude the die from the die lip 21. This increases the surface temperature of the innermost resin of the film to facilitate blocking by compression means such as nip rolls.
以上のようなインフレーションフィルム製造装置で、例
えば第2図に示すようなL−LDPE樹脂からなる内側
フィルム層2とHDPE樹脂からなる外側フィルム層3
とからなる積層フィルムを製造するには、押出し411
1・11でそれぞれ加熱溶融した所定組成のL−LDP
E樹脂及びHDPE樹脂を環状ダイス12に送り込み、
環状ダイス12の局部加熱環状ヒータ22によってダイ
リップ21の内側のL−LDPE樹脂を加熱してその表
面温度を外側のHDPE樹脂の表面温度よりも高温度の
状態で筒状に押し出す。In the above-described blown film manufacturing apparatus, for example, an inner film layer 2 made of L-LDPE resin and an outer film layer 3 made of HDPE resin as shown in FIG.
To produce a laminated film consisting of
L-LDP of a predetermined composition heated and melted in steps 1 and 11, respectively.
Feed the E resin and HDPE resin into the annular die 12,
The L-LDPE resin inside the die lip 21 is heated by the local heating annular heater 22 of the annular die 12 and extruded into a cylindrical shape with its surface temperature being higher than the surface temperature of the HDPE resin outside.
そして、送風管13から圧縮空気が送りこまれるととも
に、エアーリング14で冷却空気が吹き付けられ、(イ
)部の拡大断面図である第8図に示すように、L−LD
PE樹脂からなる内側フィルム層2とHDPE樹脂から
なる外側フィルム層3とからなり、所定径を有するチュ
ーブ状樹脂フィルム16が形成される。Then, compressed air is sent from the blast pipe 13, and cooling air is blown from the air ring 14, so that the L-LD
A tubular resin film 16 having a predetermined diameter is formed of an inner film layer 2 made of PE resin and an outer film layer 3 made of HDPE resin.
このチューブ状樹脂フィルム16は、外側フィルム層3
の最外側がスクイズロール18に接着しない程度に冷却
され、内側フィルム層2の最内側がまだ粘着性を有する
状態でガイドローラー15・・・15で案内されつつ上
昇する。そして、ガイド板17で平板状に案内された後
、引取用スクイズロールにツブロール)18・18で圧
接され、ブロッキングにより接着されて(ロ)部の拡大
断面図である第9図に示すようなブロッキング部Bで疑
似接着された4層積層フィルムに形成され、巻取機19
で巻き取られる。This tubular resin film 16 has an outer film layer 3.
is cooled to such an extent that the outermost side of the inner film layer 2 does not adhere to the squeeze roll 18, and the inner film layer 2 rises while being guided by guide rollers 15 with the innermost side still sticky. After being guided into a flat plate shape by the guide plate 17, it is pressed against the squeeze roll for take-up with tube rolls 18, 18, and adhered by blocking to form the shape shown in FIG. 9, which is an enlarged cross-sectional view of part (B). It is formed into a four-layer laminated film that is pseudo-adhered in the blocking part B, and then the winder 19
It is wound up.
次に、本発明品I、■、比較品■、■、の特性を比較し
た実験結果について説明する。Next, the results of an experiment comparing the characteristics of the invention product I, (1) and the comparative products (2), (2) will be explained.
本発明品■ 本発明品■の層構成は第1図に相当する。Invention product■ The layer structure of the product (2) of the present invention corresponds to that shown in FIG.
樹脂組成は、エチレンと4メチルペンテン−1の共重合
体樹脂である密度が0.920g/cffl、 M I
が2.1g/10分、ビカット軟化点が100’CのL
−LDPE樹脂92.4重量%、ブロッキング防止剤と
して合成シリカ0.05重量%及びオレイン酸アミド0
.05重量%、ファーネスカーボンブラック3重量%、
密度が0.923g/ad、 M Iが2.4g/10
分、ビカット軟化点が92°CのLDPE樹脂4.5重
量%(ファーネスカーボンブラック40%入りLDPE
樹脂マスターバッチ7.5重量%の形態で使用)の遮光
性LLDPE樹脂である。The resin composition is a copolymer resin of ethylene and 4-methylpentene-1, with a density of 0.920 g/cffl, M I
is 2.1g/10min, and the Vicat softening point is 100'C.
- 92.4% by weight of LDPE resin, 0.05% by weight of synthetic silica as antiblocking agent and 0 oleic acid amide
.. 05% by weight, furnace carbon black 3% by weight,
Density is 0.923g/ad, M I is 2.4g/10
4.5% by weight of LDPE resin with a Vicat softening point of 92°C (LDPE with 40% furnace carbon black)
It is a light-shielding LLDPE resin (used in the form of a resin masterbatch of 7.5% by weight).
インフレーションフィルムの成形条件は、樹脂の押出し
機のスクリュー径が50胴φ、L/Dが25、環状ダイ
スの直径が100Wφ、リップクリアランスが1鵬、ブ
ローアツプ比が1.76、引取速度12m/分である。The molding conditions for the blown film are as follows: The screw diameter of the resin extruder is 50mm, L/D is 25, the diameter of the annular die is 100W, the lip clearance is 1mm, the blow-up ratio is 1.76, and the take-up speed is 12m/min. It is.
局部加熱環状ヒータの埋め込み場所は、環状ダイリップ
からの距離が5 mm、ダイス表面から深さ15mmの
環状ダイリップ内側に設置した。The local heating annular heater was embedded inside the annular die lip at a distance of 5 mm from the annular die lip and at a depth of 15 mm from the die surface.
環状ダイリップの外側の樹脂表面温度を180°C1内
側の樹脂表面温度を局部加熱環状ヒーターの加熱により
220°Cとし、厚さ401Mで押出し、その後内側同
士が接するように折り畳んで厚さ80−の積層フィルム
とした。The resin surface temperature on the outside of the annular die lip was set to 180°C, and the resin surface temperature on the inside was set to 220°C by heating with a local heating annular heater, extruded to a thickness of 401M, and then folded so that the inner sides were in contact with each other to a thickness of 80°C. It was made into a laminated film.
比較品■ 比較品Iの層構成は第1図に相当する。Comparison product ■ The layer structure of comparative product I corresponds to that shown in FIG.
本発明品Iと同一の遮光性L−L D P E樹脂を用
い、環状ダイリップの両面の樹脂表面温度を180°C
とするほかは本発明品と全く同一の成形条件で成形した
。Using the same light-shielding L-LDPE resin as inventive product I, the resin surface temperature on both sides of the annular die lip was set at 180°C.
Except for the above, molding was performed under exactly the same molding conditions as the product of the present invention.
本発明品■ 本発明品■の層構成は第2図に相当する。Invention product■ The layer structure of the product (2) of the present invention corresponds to that shown in FIG.
内側フィルム層2の樹脂組成は、本発明品Iと同一の遮
光性L−LDPE樹脂である。The resin composition of the inner film layer 2 is the same light-shielding L-LDPE resin as the product I of the present invention.
外側フィルムN3の樹脂組成は、密度が0.954g/
c4SM rが1.1g/l、0分、ビカット軟化点が
126°CのHDPE樹脂20重量%、本発明品Iの遮
光性L−LDPE樹脂に用いたものと同一のL−LDP
E樹脂72.4重量%、オレイン酸アミド0.055重
量、合成シリカ0.05重量%およびファーネスカーボ
ンブラック3重量%と密度が0.923g/cd、MI
が2.4g/10分、ビカット軟化点が92°CのLD
PE樹脂4.5重量%(ファーネスカーボンブラック4
0%入りLDPE樹脂マスターバッチ7.5重量%の形
態で使用)の樹脂組成である。The resin composition of the outer film N3 has a density of 0.954 g/
c4SM r: 1.1 g/l, 0 min, Vicat softening point: 126°C HDPE resin 20% by weight, L-LDP same as that used for the light-shielding L-LDPE resin of the invention product I
72.4% by weight of E resin, 0.055% by weight of oleic acid amide, 0.05% by weight of synthetic silica, and 3% by weight of furnace carbon black, and a density of 0.923 g/cd, MI
2.4g/10min, LD with Vicat softening point of 92°C
PE resin 4.5% by weight (furnace carbon black 4
0% LDPE resin masterbatch (used in the form of 7.5% by weight).
二層共押出しインフレーションフィルムの成形条件は、
押出し機のスクリュー径が最外層及び最内層共に50印
φ、L/Dが20、環状ダイスの直径が5001TII
llφ、ブローフップ比が1.3、引取速度20m/分
である。The molding conditions for the two-layer coextruded blown film are as follows:
The screw diameter of the extruder is 50 marks for both the outermost layer and the innermost layer, L/D is 20, and the diameter of the annular die is 5001 TII.
llφ, the blow flop ratio was 1.3, and the take-up speed was 20 m/min.
内側フィルム層2の膜厚20溝、表面温度を局部加熱環
状ヒーターの加熱により220°Cとし、外側フィルム
層3の膜厚20頗、表面温度180°Cで環状グイリッ
プから押出し、その後内側の樹脂層同士が接するように
折り畳んで厚さ801Mの積層フィルムとした。The inner film layer 2 has a thickness of 20 mm and a surface temperature of 220°C by heating with a local heating annular heater, and the outer film layer 3 has a thickness of 20 mm and a surface temperature of 180°C and is extruded from an annular grip, and then the inner resin is heated to 220°C. It was folded so that the layers were in contact with each other to form a laminated film with a thickness of 801M.
比較品■ 比較品■の層構成は第2図に相当する。Comparison product ■ The layer structure of comparative product (■) corresponds to that shown in FIG.
本発明品■と同一の内側、外側の樹脂組成物を用いた。The same inner and outer resin compositions as in Invention Product (2) were used.
環状グイリップの内側、外側の樹脂表面温度を180”
Cとする外は本発明品■と全く同一の成形条件で成形し
た。The resin surface temperature on the inside and outside of the annular guilip is 180"
Except for C, molding was performed under exactly the same molding conditions as inventive product (2).
実験結果を第1表に示す。The experimental results are shown in Table 1.
評価は下記による。The evaluation is based on the following.
◎・・・非常に優れている
O・・・優れている
ム・・・問題あり(改良必要)
×・・・実用不可
〔発明の効果〕
本発明は、グイリップ内側に設けた局部加熱環状ヒータ
で、グイリップ最内側の樹脂を加熱しているため、従来
はブロッキング接着が困難な樹脂フィルム、使用上の問
題からブロッキングを生じさせない樹脂組成であった単
層インフレーションフィルム等もブロッキングにより接
着できる。◎...Excellent O...Excellent M...Problems (improvement required) ×...Not practical Because the resin on the innermost side of the Gurilip is heated, it is possible to bond resin films that are difficult to bond with blocking in the past, as well as single-layer blown films, which have a resin composition that does not cause blocking due to problems in use.
また、冷却条件や温湿度等の環境条件の影口を受けるこ
とが少なく、安定したブロッキングにより接着されたイ
ンフレーションフィルム成形を行うことができ、しかも
、接着面積、接着強度の異なる積層フィルムを任意に得
ることができる。In addition, it is less susceptible to the effects of environmental conditions such as cooling conditions and temperature and humidity, and it is possible to form bonded blown films with stable blocking.Moreover, laminated films with different adhesive areas and adhesive strengths can be formed at will. Obtainable.
さらに、従来は成形時の樹脂の温度を高めると押出し機
内や環状ダイス内で劣化やゲル化が発生し、フィルムに
フィッシュアイやピンホールが発生し、バブルの不安定
やドローダウンが発生する等のインフレーションフィル
ム成形不良が生ずるため樹脂温度を矯めることが困難で
あったが、本発明ではダイリップの局所的加熱であるた
め上記問題を発生することな(ダイリップ部の樹脂の流
動を良好にして押出し機のモーター負荷を減することが
できる。Furthermore, in the past, when the temperature of the resin during molding was raised, deterioration and gelation occurred in the extruder and annular die, fish eyes and pinholes appeared in the film, unstable bubbles and drawdown occurred, etc. However, in the present invention, since the die lip is heated locally, the above problem does not occur (by improving the flow of the resin at the die lip), it is difficult to control the resin temperature. Extruder motor load can be reduced.
第1図から第4図は本発明による積層フィルムの実施例
の層構成を示す部分断面図、第5図は本発明による積層
フィルムを製造する装置の概略図、第6図は同上環状ダ
イスの横断面図、第7図は同上縁断面図、第8図は第5
図中(イ)部の拡大断面図、第9図は第5図中(I+)
部の拡大断面図である。
11・・・押出し機
12・・・環状ダイス
21・・・ダイリップ
22・・・局部加熱環状ヒータ
Bはブロッキング接着部位を示す。
特許出願人 冨士写真フィルム株式会社代 理 人
弁理士 田中 政治 はか1名・・・単層インフレー
ションフィルム
・・・内側フィルム
・・・外側フィルム
・・・2層共押出しインフレーションフィルム・・・3
N共押出しインフレーションフィルム第
図
弔
図
弔
図
6口)1 to 4 are partial cross-sectional views showing the layer structure of an embodiment of the laminated film according to the present invention, FIG. 5 is a schematic diagram of an apparatus for manufacturing the laminated film according to the present invention, and FIG. A cross-sectional view, Figure 7 is a cross-sectional view of the same upper edge, and Figure 8 is a cross-sectional view of the same upper edge.
An enlarged sectional view of part (A) in the figure, Figure 9 is (I+) in Figure 5.
FIG. 11... Extruder 12... Annular die 21... Die lip 22... Local heating annular heater B indicates a blocking adhesion site. Patent applicant: Fuji Photo Film Co., Ltd. Agent
Patent attorney Masami Tanaka (1 person)...Single-layer blown film...Inner film...Outer film...Two-layer coextruded blown film...3
N coextrusion blown film Figure 6)
Claims (2)
イリップ内側近傍に設けられた局部加熱環状ヒータで加
熱し、押し出した樹脂をブロッキングにより接着したこ
とを特徴とする積層フィルム(1) A laminated film characterized in that when it is extruded from the die lip of an annular die, it is heated by a local heating annular heater installed near the inside of the die lip, and the extruded resin is bonded by blocking.
加熱環状ヒータで、最内側の樹脂の表面温度を最外側の
樹脂の表面温度より高くなるように加熱しつつダイリッ
プから樹脂を押し出し、その後最内側同士をブロッキン
グにより接着させることを特徴とする積層フィルムの製
造方法(2) A locally heated annular heater installed near the inside of the die lip of the annular die extrudes the resin from the die lip while heating the innermost resin so that the surface temperature is higher than that of the outermost resin, and then extrudes the resin from the die lip. A method for producing a laminated film characterized by adhering the inner sides to each other by blocking.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63283891A JPH0714615B2 (en) | 1988-11-11 | 1988-11-11 | Laminated film and manufacturing method thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63283891A JPH0714615B2 (en) | 1988-11-11 | 1988-11-11 | Laminated film and manufacturing method thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02130119A true JPH02130119A (en) | 1990-05-18 |
JPH0714615B2 JPH0714615B2 (en) | 1995-02-22 |
Family
ID=17671520
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63283891A Expired - Fee Related JPH0714615B2 (en) | 1988-11-11 | 1988-11-11 | Laminated film and manufacturing method thereof |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0714615B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0351843A (en) * | 1989-07-19 | 1991-03-06 | Konica Corp | Laminate |
KR20210061133A (en) * | 2019-11-19 | 2021-05-27 | 주식회사 마린이노베이션 | Manufacturing method of eco-friendly plastic bags using seaweeds and vegetable raw materials |
WO2021101094A1 (en) * | 2019-11-19 | 2021-05-27 | 주식회사 마린이노베이션 | Eco-friendly plastic bag using seaweed and vegetable raw material and manufacturing method therefor |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5293482A (en) * | 1976-02-02 | 1977-08-05 | Mitsubishi Chem Ind | Method of manufacturing mono dimensional poly ethylene film |
-
1988
- 1988-11-11 JP JP63283891A patent/JPH0714615B2/en not_active Expired - Fee Related
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5293482A (en) * | 1976-02-02 | 1977-08-05 | Mitsubishi Chem Ind | Method of manufacturing mono dimensional poly ethylene film |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0351843A (en) * | 1989-07-19 | 1991-03-06 | Konica Corp | Laminate |
KR20210061133A (en) * | 2019-11-19 | 2021-05-27 | 주식회사 마린이노베이션 | Manufacturing method of eco-friendly plastic bags using seaweeds and vegetable raw materials |
WO2021101094A1 (en) * | 2019-11-19 | 2021-05-27 | 주식회사 마린이노베이션 | Eco-friendly plastic bag using seaweed and vegetable raw material and manufacturing method therefor |
Also Published As
Publication number | Publication date |
---|---|
JPH0714615B2 (en) | 1995-02-22 |
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