WO2022113566A1 - Ptp用蓋材およびptp包装体 - Google Patents
Ptp用蓋材およびptp包装体 Download PDFInfo
- Publication number
- WO2022113566A1 WO2022113566A1 PCT/JP2021/038438 JP2021038438W WO2022113566A1 WO 2022113566 A1 WO2022113566 A1 WO 2022113566A1 JP 2021038438 W JP2021038438 W JP 2021038438W WO 2022113566 A1 WO2022113566 A1 WO 2022113566A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- ptp
- lid material
- polypropylene
- layer
- resin
- Prior art date
Links
- 239000000463 material Substances 0.000 title claims abstract description 245
- -1 polypropylene Polymers 0.000 claims abstract description 58
- 229920005989 resin Polymers 0.000 claims abstract description 55
- 239000011347 resin Substances 0.000 claims abstract description 55
- 239000004743 Polypropylene Substances 0.000 claims abstract description 53
- 229920001155 polypropylene Polymers 0.000 claims abstract description 43
- 238000002844 melting Methods 0.000 claims abstract description 20
- 230000008018 melting Effects 0.000 claims abstract description 20
- 239000013078 crystal Substances 0.000 claims abstract description 17
- 239000010410 layer Substances 0.000 claims description 98
- 229920005673 polypropylene based resin Polymers 0.000 claims description 51
- 238000012360 testing method Methods 0.000 claims description 24
- 238000006073 displacement reaction Methods 0.000 claims description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
- 229920000098 polyolefin Polymers 0.000 claims description 16
- 229920001971 elastomer Polymers 0.000 claims description 15
- 239000000806 elastomer Substances 0.000 claims description 15
- 239000000126 substance Substances 0.000 claims description 13
- 239000002344 surface layer Substances 0.000 claims description 13
- 230000005540 biological transmission Effects 0.000 claims description 12
- 229920005678 polyethylene based resin Polymers 0.000 claims description 9
- 238000000034 method Methods 0.000 description 58
- 238000007789 sealing Methods 0.000 description 28
- 230000000052 comparative effect Effects 0.000 description 21
- 238000005259 measurement Methods 0.000 description 17
- 238000004519 manufacturing process Methods 0.000 description 16
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
- 239000003054 catalyst Substances 0.000 description 12
- 238000011156 evaluation Methods 0.000 description 12
- 238000000465 moulding Methods 0.000 description 11
- 230000009467 reduction Effects 0.000 description 10
- 230000004888 barrier function Effects 0.000 description 9
- 238000006116 polymerization reaction Methods 0.000 description 9
- 230000003014 reinforcing effect Effects 0.000 description 9
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 8
- 239000004698 Polyethylene Substances 0.000 description 8
- 239000004793 Polystyrene Substances 0.000 description 8
- 238000001816 cooling Methods 0.000 description 8
- 239000000178 monomer Substances 0.000 description 8
- 230000000704 physical effect Effects 0.000 description 8
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 7
- 238000002835 absorbance Methods 0.000 description 7
- 239000004711 α-olefin Substances 0.000 description 7
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 6
- 238000002425 crystallisation Methods 0.000 description 6
- 230000008025 crystallization Effects 0.000 description 6
- 229920000573 polyethylene Polymers 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 5
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 5
- 229920000219 Ethylene vinyl alcohol Polymers 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 5
- 239000003484 crystal nucleating agent Substances 0.000 description 5
- 239000005038 ethylene vinyl acetate Substances 0.000 description 5
- 238000004806 packaging method and process Methods 0.000 description 5
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 5
- 239000004800 polyvinyl chloride Substances 0.000 description 5
- 229920000915 polyvinyl chloride Polymers 0.000 description 5
- 238000012545 processing Methods 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 4
- 239000005977 Ethylene Substances 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 230000032798 delamination Effects 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 4
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 4
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 4
- 239000002356 single layer Substances 0.000 description 4
- PBKONEOXTCPAFI-UHFFFAOYSA-N 1,2,4-trichlorobenzene Chemical compound ClC1=CC=C(Cl)C(Cl)=C1 PBKONEOXTCPAFI-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 238000000137 annealing Methods 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 230000003247 decreasing effect Effects 0.000 description 3
- 230000002950 deficient Effects 0.000 description 3
- 230000002542 deteriorative effect Effects 0.000 description 3
- 230000007613 environmental effect Effects 0.000 description 3
- UFRKOOWSQGXVKV-UHFFFAOYSA-N ethene;ethenol Chemical compound C=C.OC=C UFRKOOWSQGXVKV-UHFFFAOYSA-N 0.000 description 3
- 239000004715 ethylene vinyl alcohol Substances 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 238000005227 gel permeation chromatography Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 3
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920013716 polyethylene resin Polymers 0.000 description 3
- 229920005672 polyolefin resin Polymers 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- 230000005855 radiation Effects 0.000 description 3
- 238000004064 recycling Methods 0.000 description 3
- 239000011342 resin composition Substances 0.000 description 3
- 239000000565 sealant Substances 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- 238000007740 vapor deposition Methods 0.000 description 3
- 150000007934 α,β-unsaturated carboxylic acids Chemical class 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 2
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1-dodecene Chemical compound CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 2
- 229920001342 Bakelite® Polymers 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- 241000209094 Oryza Species 0.000 description 2
- 235000007164 Oryza sativa Nutrition 0.000 description 2
- 238000001069 Raman spectroscopy Methods 0.000 description 2
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 239000003463 adsorbent Substances 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 229910000323 aluminium silicate Inorganic materials 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 2
- LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical compound C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- MTZQAGJQAFMTAQ-UHFFFAOYSA-N ethyl benzoate Chemical compound CCOC(=O)C1=CC=CC=C1 MTZQAGJQAFMTAQ-UHFFFAOYSA-N 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 230000010354 integration Effects 0.000 description 2
- 239000011229 interlayer Substances 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
- 239000000825 pharmaceutical preparation Substances 0.000 description 2
- 229940127557 pharmaceutical product Drugs 0.000 description 2
- 239000002985 plastic film Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 230000000379 polymerizing effect Effects 0.000 description 2
- 229920005990 polystyrene resin Polymers 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 229920001384 propylene homopolymer Polymers 0.000 description 2
- 230000010349 pulsation Effects 0.000 description 2
- 235000009566 rice Nutrition 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 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
- 229920003067 (meth)acrylic acid ester copolymer Polymers 0.000 description 1
- MHNNAWXXUZQSNM-UHFFFAOYSA-N 2-methylbut-1-ene Chemical compound CCC(C)=C MHNNAWXXUZQSNM-UHFFFAOYSA-N 0.000 description 1
- YHQXBTXEYZIYOV-UHFFFAOYSA-N 3-methylbut-1-ene Chemical compound CC(C)C=C YHQXBTXEYZIYOV-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- MXRIRQGCELJRSN-UHFFFAOYSA-N O.O.O.[Al] Chemical compound O.O.O.[Al] MXRIRQGCELJRSN-UHFFFAOYSA-N 0.000 description 1
- JHQYNYXQKSKNAK-UHFFFAOYSA-N OP(O)O.OP(O)O Chemical compound OP(O)O.OP(O)O JHQYNYXQKSKNAK-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- 229920001659 Renewable Polyethylene Polymers 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 150000008065 acid anhydrides Chemical class 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
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons 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
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 229920006378 biaxially oriented polypropylene Polymers 0.000 description 1
- 239000011127 biaxially oriented polypropylene Substances 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- QYMGIIIPAFAFRX-UHFFFAOYSA-N butyl prop-2-enoate;ethene Chemical compound C=C.CCCCOC(=O)C=C QYMGIIIPAFAFRX-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 239000012986 chain transfer agent Substances 0.000 description 1
- 235000019219 chocolate Nutrition 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 238000011437 continuous method Methods 0.000 description 1
- 238000003851 corona treatment Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- CFBGXYDUODCMNS-UHFFFAOYSA-N cyclobutene Chemical compound C1CC=C1 CFBGXYDUODCMNS-UHFFFAOYSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000003795 desorption Methods 0.000 description 1
- 238000000113 differential scanning calorimetry Methods 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 229940069096 dodecene Drugs 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 229920006245 ethylene-butyl acrylate Polymers 0.000 description 1
- 229920006244 ethylene-ethyl acrylate Polymers 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000001595 flow curve Methods 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 238000012685 gas phase polymerization Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 239000011086 glassine Substances 0.000 description 1
- 238000003988 headspace gas chromatography Methods 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
- 239000003317 industrial substance Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 230000001678 irradiating effect 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
- 230000007774 longterm Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 238000009832 plasma treatment Methods 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002493 poly(chlorotrifluoroethylene) Polymers 0.000 description 1
- 239000005023 polychlorotrifluoroethylene (PCTFE) polymer Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 230000037048 polymerization activity Effects 0.000 description 1
- 229920005606 polypropylene copolymer Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- YONPGGFAJWQGJC-UHFFFAOYSA-K titanium(iii) chloride Chemical compound Cl[Ti](Cl)Cl YONPGGFAJWQGJC-UHFFFAOYSA-K 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D75/00—Packages comprising articles or materials partially or wholly enclosed in strips, sheets, blanks, tubes, or webs of flexible sheet material, e.g. in folded wrappers
- B65D75/28—Articles or materials wholly enclosed in composite wrappers, i.e. wrappers formed by associating or interconnecting two or more sheets or blanks
- B65D75/30—Articles or materials enclosed between two opposed sheets or blanks having their margins united, e.g. by pressure-sensitive adhesive, crimping, heat-sealing, or welding
- B65D75/32—Articles or materials enclosed between two opposed sheets or blanks having their margins united, e.g. by pressure-sensitive adhesive, crimping, heat-sealing, or welding one or both sheets or blanks being recessed to accommodate contents
- B65D75/36—Articles or materials enclosed between two opposed sheets or blanks having their margins united, e.g. by pressure-sensitive adhesive, crimping, heat-sealing, or welding one or both sheets or blanks being recessed to accommodate contents one sheet or blank being recessed and the other formed of relatively stiff flat sheet material, e.g. blister packages, the recess or recesses being preformed
- B65D75/367—Articles or materials enclosed between two opposed sheets or blanks having their margins united, e.g. by pressure-sensitive adhesive, crimping, heat-sealing, or welding one or both sheets or blanks being recessed to accommodate contents one sheet or blank being recessed and the other formed of relatively stiff flat sheet material, e.g. blister packages, the recess or recesses being preformed and forming several compartments
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D75/00—Packages comprising articles or materials partially or wholly enclosed in strips, sheets, blanks, tubes, or webs of flexible sheet material, e.g. in folded wrappers
- B65D75/28—Articles or materials wholly enclosed in composite wrappers, i.e. wrappers formed by associating or interconnecting two or more sheets or blanks
- B65D75/30—Articles or materials enclosed between two opposed sheets or blanks having their margins united, e.g. by pressure-sensitive adhesive, crimping, heat-sealing, or welding
- B65D75/32—Articles or materials enclosed between two opposed sheets or blanks having their margins united, e.g. by pressure-sensitive adhesive, crimping, heat-sealing, or welding one or both sheets or blanks being recessed to accommodate contents
- B65D75/325—Articles or materials enclosed between two opposed sheets or blanks having their margins united, e.g. by pressure-sensitive adhesive, crimping, heat-sealing, or welding one or both sheets or blanks being recessed to accommodate contents one sheet being recessed, and the other being a flat not- rigid sheet, e.g. puncturable or peelable foil
- B65D75/327—Articles or materials enclosed between two opposed sheets or blanks having their margins united, e.g. by pressure-sensitive adhesive, crimping, heat-sealing, or welding one or both sheets or blanks being recessed to accommodate contents one sheet being recessed, and the other being a flat not- rigid sheet, e.g. puncturable or peelable foil and forming several compartments
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/30—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
- B32B27/304—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers comprising vinyl halide (co)polymers, e.g. PVC, PVDC, PVF, PVDF
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B3/00—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form
- B32B3/26—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form characterised by a particular shape of the outline of the cross-section of a continuous layer; characterised by a layer with cavities or internal voids ; characterised by an apertured layer
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D65/00—Wrappers or flexible covers; Packaging materials of special type or form
- B65D65/38—Packaging materials of special type or form
- B65D65/40—Applications of laminates for particular packaging purposes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D77/00—Packages formed by enclosing articles or materials in preformed containers, e.g. boxes, cartons, sacks or bags
- B65D77/10—Container closures formed after filling
- B65D77/20—Container closures formed after filling by applying separate lids or covers, i.e. flexible membrane or foil-like covers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/10—Homopolymers or copolymers of propene
- C08L23/12—Polypropene
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2250/00—Layers arrangement
- B32B2250/24—All layers being polymeric
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2255/00—Coating on the layer surface
- B32B2255/10—Coating on the layer surface on synthetic resin layer or on natural or synthetic rubber layer
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2255/00—Coating on the layer surface
- B32B2255/20—Inorganic coating
- B32B2255/205—Metallic coating
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2274/00—Thermoplastic elastomer material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/50—Properties of the layers or laminate having particular mechanical properties
- B32B2307/514—Oriented
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/50—Properties of the layers or laminate having particular mechanical properties
- B32B2307/514—Oriented
- B32B2307/516—Oriented mono-axially
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/50—Properties of the layers or laminate having particular mechanical properties
- B32B2307/54—Yield strength; Tensile strength
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/50—Properties of the layers or laminate having particular mechanical properties
- B32B2307/58—Cuttability
- B32B2307/581—Resistant to cut
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/70—Other properties
- B32B2307/704—Crystalline
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/70—Other properties
- B32B2307/724—Permeability to gases, adsorption
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/70—Other properties
- B32B2307/724—Permeability to gases, adsorption
- B32B2307/7242—Non-permeable
- B32B2307/7246—Water vapor barrier
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/70—Other properties
- B32B2307/732—Dimensional properties
- B32B2307/737—Dimensions, e.g. volume or area
- B32B2307/7375—Linear, e.g. length, distance or width
- B32B2307/7376—Thickness
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2435/00—Closures, end caps, stoppers
- B32B2435/02—Closures, end caps, stoppers for containers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D2565/00—Wrappers or flexible covers; Packaging materials of special type or form
- B65D2565/38—Packaging materials of special type or form
- B65D2565/381—Details of packaging materials of special type or form
- B65D2565/387—Materials used as gas barriers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
- C08L2205/025—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group containing two or more polymers of the same hierarchy C08L, and differing only in parameters such as density, comonomer content, molecular weight, structure
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W30/00—Technologies for solid waste management
- Y02W30/50—Reuse, recycling or recovery technologies
- Y02W30/80—Packaging reuse or recycling, e.g. of multilayer packaging
Definitions
- the present invention relates to a lid material for PTP (press-through pack) and a PTP package.
- a PTP package having a bottom material and a lid material As one of the packaging forms for pharmaceuticals and foods, a PTP package having a bottom material and a lid material is known.
- a bottom material having a pocket-shaped recess is formed by vacuum molding or pressure molding a plastic sheet made of a polyvinyl chloride resin, a polypropylene resin, or the like, and the recess is filled with the contents.
- Manufactured by heat-sealing the lid material to the flange portion, which is a portion other than the recess.
- the stored contents can be taken out by applying a force to the contents from the outside of the bottom material toward the lid material to break through the lid material.
- Patent Document 1 describes a lid having a press-through function, which uses a polypropylene-based resin film and a reinforcing resin layer laminated on the polypropylene-based resin film as a base material, and deteriorates the polypropylene-based resin film by irradiation with radiation.
- the material is disclosed.
- Patent Documents 2 and 3 disclose a lid material for PTP based on a sheet made of a resin composition containing a polypropylene-based resin and an inorganic substance (talc or the like) for improving projectability. ..
- Patent Document 4 contains a crystalline thermoplastic resin as an essential component and crystallizes by heat treatment in order to have easy incineration property that can be processed under the same conditions as the bottom material and to exhibit excellent tensile cutting load, elongation and easy breakthrough property.
- a sheet for a lid material of a crystallized blister pack package is disclosed.
- Patent Document 5 discloses a laminated polypropylene-based film in which a resin having a certain range of heat of crystal melting is laminated on an interlayer portion in order to improve the interlayer adhesive strength in addition to hand-cutting property and mechanical strength.
- Patent Document 6 in order to facilitate disposal after use and improve press-through property and print readability, a plastic lid material film for PTP using a styrene resin and an inorganic filler and a PTP packaging using the same. The body is disclosed.
- Japanese Unexamined Patent Publication No. 7-256842 Japanese Unexamined Patent Publication No. 10-101133 Japanese Unexamined Patent Publication No. 9-11422 Japanese Unexamined Patent Publication No. 2000-7026 Japanese Unexamined Patent Publication No. 2000-25173 Japanese Unexamined Patent Publication No. 2013-234002
- the lid material described in Patent Document 4 has room for improvement in terms of the above-mentioned open recognition, and is laminated with different resins such as polystyrene, ethylene-vinyl acetate copolymer saken, and nylon-6. Therefore, there is a problem that it is not suitable for material recycling. Since the lid material described in Patent Document 5 is laminated with a biaxially oriented polypropylene-based resin, there is a problem that the sticking property and the opening recognition property are deteriorated. Since the lid material described in Patent Document 6 uses a styrene resin, it is not suitable for recycling, and since an emulsion type heat sealant is applied, an unpleasant odor is generated in a high temperature environment. There is a problem of doing.
- an object of the present invention is to provide a lid material for a PTP package and a PTP package which are excellent in sticking out property and open recognition property and which suppresses an unpleasant odor.
- the present inventors have solved the above-mentioned problems by using a polypropylene-based resin having a specific range of molecular weight and a lid material for PTP having a specific range of heat of crystal melting. We have found that it can be solved and have completed the present invention.
- the present invention is as follows.
- Cover material [2] The PTP lid material according to [1], wherein the MD orientation degree is ⁇ 0.035 to 0.035.
- the thickness is 10 to 100 ⁇ m
- the water vapor transmission rate is 10 g / m2 ⁇ day or less
- the tensile strength is 20 to 50 MPa for both MD and TD
- the tensile elongation is 15% or less for both MD and TD.
- the lid material for PTP according to any one of [1] to [4], which contains 0.1 to 3% by mass of an inorganic substance.
- the lid material for PTP according to any one of [1] to [5], which comprises a layer containing the polypropylene-based resin and at least one surface layer containing a polyethylene-based resin, a polypropylene-based resin, or a polyolefin-based elastomer.
- a PTP package comprising the PTP lid material according to any one of [1] to [6] and a bottom material having a recess for accommodating the contents.
- a lid material for a PTP package and a PTP package which are excellent in sticking out property and open recognition property and suppress an unpleasant odor.
- FIG. 1 is a cross-sectional view showing an embodiment of a PTP package provided with a PTP lid material according to the present invention.
- FIG. 2 is a graph showing an example of a load-displacement curve obtained when a puncture test is performed on a PTP lid material according to the present invention.
- the present embodiment will be described in detail, but the present invention is not limited to the following description and varies within the scope of the gist thereof. It can be transformed and implemented.
- the PTP lid material (hereinafter, also simply referred to as “cover material”) of the present embodiment contains a polypropylene-based resin having a weight average molecular weight of 2.0 ⁇ 10 5 to 3.5 ⁇ 105, and is differential scanning. It is characterized in that the amount of heat of crystal melting by a calorimeter (DSC) is 70 J / g or more.
- the polypropylene-based resin contained in the lid material for PTP of the present embodiment is not particularly limited as long as the weight average molecular weight is 2.0 ⁇ 10 5 to 3.5 ⁇ 105 , and for example, a propylene homopolymer. Examples thereof include copolymers of propylene and other monomers, and modified products thereof. Further, from the viewpoint of environmental friendliness, biopolypropylene may be used. Of these, propylene homopolymers are preferable from the viewpoints of heat resistance, water vapor barrier property, and tensile elongation.
- the polypropylene-based resin may be used alone or in combination of two or more.
- Examples of the monomer copolymerizable with propylene include ⁇ -olefins such as ethylene, 1-butene, isobutylene, 1-pentene, and 1-hexene.
- the polymerization form is not particularly limited, and may be a random copolymer, a block copolymer, or the like.
- the method for producing the polypropylene-based resin is not particularly limited, and a known method such as a method for polymerizing propylene or other monomers in the presence of a catalyst can be used. Specific examples thereof include a method of polymerizing propylene and other monomers in the presence of a catalyst and an alkylaluminum compound at a polymerization temperature of 0 to 100 ° C. and a polymerization pressure of 3 to 100 atm.
- the catalyst include a titanium trichloride catalyst, a titanium halide catalyst supported on a carrier such as magnesium chloride, and the like.
- a chain transfer agent such as hydrogen may be added to adjust the molecular weight of the polymer.
- an electron-donating compound can be used as an internal donor component or an external donor component as a third component in order to enhance the isotacticity and polymerization activity of polypropylene.
- the electron donating compound is not particularly limited, and known compounds can be used.
- ester compounds such as ⁇ -caprolactone, methyl methacrylate, ethyl benzoate, methyl tolulate and the like; triphenyl phosphite, phosphite phosphite, etc. can be used.
- Subphosphate esters such as tributyl; Phosphoric acid derivatives such as hexamethylphosphoric triamide; alkoxy ester compounds; Aromatic monocarboxylic acid esters; Aromatic alkylalkoxysilanes; aliphatic hydrocarbon alkoxysilanes; Various ether compounds; Various alcoholskind: Various phenols and the like can be mentioned.
- the polymerization method in the above method may be either a batch method or a continuous method.
- Examples of the polymerization method include solution polymerization under a solvent such as butane, pentane, hexane, heptane, and octane, slurry polymerization, massive polymerization in a monomer under no solvent, and gas phase polymerization in a gaseous monomer. ..
- the polypropylene-based resin may be an unmodified polypropylene-based resin modified with a modifying agent such as ⁇ , ⁇ -unsaturated carboxylic acid or a derivative thereof (including acid anhydride and ester).
- a modifying agent such as ⁇ , ⁇ -unsaturated carboxylic acid or a derivative thereof (including acid anhydride and ester).
- the modified polypropylene-based resin include those obtained by grafting or adding an unmodified polypropylene-based resin with ⁇ , ⁇ -unsaturated carboxylic acid or a derivative thereof. Specific examples thereof include those in which ⁇ , ⁇ -unsaturated carboxylic acid or a derivative thereof is grafted or added to the polypropylene resin at a ratio of about 0.01 to 10% by mass of the total polypropylene resin. ..
- the modified polypropylene-based resin reacts the unmodified polypropylene-based resin with the modifying agent in the range of 30 to 350 ° C., for example, in the presence or absence of a radical generator, in a molten state, in a solution state, or in a slurry state. Obtained by letting.
- the mixing ratio of the unmodified polypropylene and the modified polypropylene is not particularly limited and may be any ratio.
- the weight average molecular weight of the polypropylene-based resin is 2.0 ⁇ 10 5 to 3.5 ⁇ 105, preferably 2.2 ⁇ 10 5 to 3.2 ⁇ 10 5 , and more preferably 2.3 ⁇ 10 5 . It is ⁇ 3.0 ⁇ 105 .
- a polypropylene resin having a weight average molecular weight in the above range is not usually used for a film because of its fragility, but the PTP lid material of the present embodiment takes advantage of this fragility and has excellent projectability. ..
- the weight average molecular weight can be measured by gel permeation chromatography (hereinafter, also referred to as “GPC”), and specifically, can be measured by the method described in Examples described later. ..
- the content of the polypropylene-based resin is preferably 60 to 100% by mass, more preferably 70 to 95% by mass, still more preferably 75 to 90% by mass, with the PTP lid material as 100% by mass. be.
- the content of the polypropylene-based resin is in the above range, good projectivity tends to be easily exhibited. Further, in particular, when the content of the polypropylene-based resin is 100% by mass, the lid material has excellent recyclability.
- the lid material for PTP of the present embodiment may be a laminate having a layer containing the above-mentioned polypropylene-based resin (hereinafter, also referred to as “low molecular weight polypropylene-based resin layer”).
- Other layers laminated on the low molecular weight polypropylene resin layer include, for example, a sealing layer for improving the sealing property with the bottom material for PTP, and an adjusting layer for adjusting the physical properties of the lid material such as strength and protrusion. Examples thereof include a reinforcing layer for preventing film breakage during packaging, a barrier layer for improving gas barrier properties, and the like.
- the number of layers is not particularly limited, but is preferably 2 to 5 layers, more preferably 2 to 3 layers, from the viewpoint of the balance between strength, protrusion property, water vapor barrier property, sealing property, and recyclability. ..
- the thickness of the low molecular weight polypropylene-based resin layer is preferably 60 to 95%, more preferably 70 to 95%, still more preferably 75 to 90%, with the total thickness of the PTP lid material being 100%. be.
- the thickness of the low molecular weight polypropylene-based resin layer is in the above range, it tends to easily exhibit good protrusion property and water vapor barrier property.
- the lid material for PTP of the present embodiment may include a layer containing the above-mentioned polypropylene-based resin and at least one surface layer containing a polyethylene-based resin, a polypropylene-based resin, or a polyolefin-based elastomer.
- the surface layer may be either one or both of the surface layer on the bottom material side and the outer surface layer (outermost layer) adhered to the bottom material.
- an outer surface layer may be used as a reinforcing layer for preventing the film from breaking during packaging.
- the heat-sealing property is excellent, and since these resins can be co-extruded, it is not necessary to apply an emulsion-type heat-sealing agent, and the environment is high. However, since no unpleasant odor is generated, it is suitable as a surface layer on the bottom material side to be adhered to the bottom material.
- a layer containing a polyolefin-based elastomer is preferable because it is particularly excellent in low-temperature sealing property, and from the viewpoint of recyclability, a polypropylene-based resin is used so that the entire lid material for PTP is composed of a polypropylene-based resin. It is preferably a layer containing.
- the thickness of the surface layer is preferably 5 to 40%, more preferably 5 to 30%, still more preferably 10 to 25%, with the thickness of the entire PTP lid material as 100%. When the thickness of the surface layer is within the above range, good heat-sealing properties can be imparted and film breakage can be prevented without deteriorating the projecting property.
- the polyethylene-based resin contained in the surface layer is not particularly limited and may be either an ethylene homopolymer or a copolymer of ethylene and another monomer.
- an ethylene homopolymer an ethylene-propylene copolymer.
- Ethylene-butene copolymer ethylene- ⁇ -olefin copolymer such as ethylene-octene copolymer; ethylene-ethyl acrylate copolymer, ethylene-butyl acrylate copolymer, ethylene-ethyl acrylate-methyl methacrylate copolymer
- examples thereof include ethylene- (meth) acrylic acid ester copolymers and the like; ethylene-vinyl acetate copolymers and the like.
- a low-density ethylene- ⁇ -olefin copolymer is preferable because the lower the density, the better the low-temperature sealing property tends to be.
- biopolyethylene may be used.
- the polyethylene-based resin may be used alone or in combination of two or more.
- the method for producing the polyethylene-based resin is not particularly limited, and polymerization can be carried out using a known catalyst such as a single-site catalyst or a multi-site catalyst.
- the content of the polyethylene-based resin is preferably 5 to 40% by mass, more preferably 5 to 30% by mass, and further preferably 10 to 25% by mass, with the PTP lid material as 100% by mass. ..
- the content of the polyethylene-based resin is within the above range, good heat-sealing properties can be imparted and film breakage can be prevented without deteriorating the projecting property.
- Examples of the polypropylene-based resin contained in the surface layer include the same types as the above-mentioned low molecular weight polypropylene-based resin. Above all, a low-density propylene- ⁇ -olefin copolymer is preferable from the viewpoint of excellent low-temperature sealing property.
- the molecular weight of the polypropylene-based resin is not particularly limited, but is preferably higher than that of the polypropylene-based resin contained in the above-mentioned low molecular weight polypropylene-based resin layer.
- the melt flow rate (measured at 230 ° C. and a load of 2.16 kgf according to ASTM D-1238, MFR) is 3 to 15 g / 10 minutes.
- the polypropylene-based resin may be used alone or in combination of two or more.
- the polyolefin-based elastomer is a low-crystalline to amorphous olefin-based polymer having a crystallinity of 50% or less, and examples of the monomer (olefin) of the polyolefin-based elastomer include ethylene, propylene, 1-butene, and isobutylene. , 1-pentene, 1-hexene, 4-methyl-1-pentene, 3-methyl-1-butene, 2-methyl-1-butene, 1-hexene, 1-octene, 1-decene, 1-dodecene, etc.
- Cyclic olefins such as ⁇ -olefin, cyclobutene, cyclopentene, and cyclohexene can be mentioned.
- polypropylene-based elastomers having a low melting point 55 to 90 ° C.
- a biopolyolefin-based elastomer may be used.
- the polyolefin-based elastomer may be used alone or in combination of two or more.
- the method for producing the polyolefin-based elastomer is not particularly limited, and polymerization can be carried out using a known catalyst such as a single-site catalyst or a multi-site catalyst.
- the content of the polyolefin-based elastomer is preferably 5 to 40% by mass, more preferably 5 to 30% by mass, and further preferably 10 to 25% by mass, with the PTP lid material as 100% by mass. ..
- the content of the polyolefin-based elastomer is within the above range, good heat-sealing properties can be imparted and film breakage can be prevented without deteriorating the projecting property.
- the PTP lid material of the present embodiment has an adjusting layer for adjusting the physical properties of the lid material such as strength and protrusion between the above-mentioned low molecular weight polypropylene resin layer and the surface layer. It may be included.
- the thickness of the adjusting layer is preferably 10 to 40%, more preferably 15 to 35%, still more preferably 20 to 30%, with the thickness of the entire PTP lid material as 100%.
- polypropylene resin for the adjusting layer.
- the type of polypropylene-based resin include those similar to the above-mentioned low molecular weight polypropylene-based resin.
- the molecular weight of the polypropylene-based resin is not particularly limited, but is preferably higher than that of the polypropylene-based resin contained in the above-mentioned low molecular weight polypropylene-based resin layer.
- the melt flow rate (measured at 230 ° C. and a load of 2.16 kgf according to ASTM D-1238, MFR) is 3 to 15 g / 10 minutes.
- the polypropylene-based resin may be used alone or in combination of two or more.
- the lid material for PTP of the present embodiment may contain an inorganic substance in order to increase the starting point of fracture and improve the projectability.
- the inorganic substance is not particularly limited, and examples thereof include amorphous alumina silicate, silica, alumina, talc, kaolin, mica, wallastnite, clay, calcium carbonate, glass fiber, and aluminum sulfate.
- the content of the inorganic substance is preferably 0.1 to 3% by mass, more preferably 0.3 to 2% by mass, still more preferably 0.5 to 1 by mass, assuming that the lid material for PTP is 100% by mass. It is mass%.
- the lid material exhibits good projecting property, has few impurities, and is highly recyclable.
- the lid material for PTP of the present embodiment is an additive usually used in the art, for example, a metal soap, a colorant, a plasticizer, an antioxidant, a heat stabilizer, an ultraviolet absorber, which assists in the dispersion of the above-mentioned inorganic substances. It may contain a lubricant, an antistatic agent, a crystal nucleating agent and the like. Further, the PTP lid material of the present embodiment may be subjected to treatments such as corona treatment, plasma treatment, ultraviolet treatment, and AC (anchor coating) treatment for the purpose of improving printing characteristics. In particular, white colorants and printing are preferable for the following reasons.
- the thickness of the PTP lid material of the present embodiment is preferably 10 to 100 ⁇ m, more preferably 30 to 80 ⁇ m, and further preferably 40 to 60 ⁇ m.
- the thickness is 10 ⁇ m or more, the tensile strength and the water vapor barrier property that can withstand the processing step are easily exhibited, and when the thickness is 100 ⁇ m or less, good protrusion property is easily exhibited.
- the water vapor transmission rate of the PTP lid material of the present embodiment is preferably 10 g / m 2 ⁇ day or less, more preferably 8 g / m 2 ⁇ day or less, and further preferably 5 g / m 2 ⁇ day or less. Is. When the water vapor transmission rate is within the above range, it is possible to prevent the contents of pharmaceutical products and the like from being denatured by water vapor, and long-term storage is possible.
- the water vapor transmission rate of the PTP lid material can be adjusted by, for example, the thickness of the PTP lid material, the selection of the type of resin, the presence or absence of the barrier layer, and the like.
- the water vapor transmission rate tends to decrease.
- the barrier layer include a resin layer such as an ethylene-vinyl alcohol copolymer and a cyclic olefin, and an inorganic vapor deposition layer such as aluminum, aluminum oxide and silicon oxide.
- a resin having a high degree of crystallinity the water vapor transmission rate of the PTP lid material can be lowered.
- the water vapor transmission rate is a value measured in accordance with JIS K7129 and converted into a thickness of 40 ⁇ m, and can be specifically obtained by the method described in Examples described later.
- the MD tensile strength of the PTP lid material of the present embodiment is preferably 20 to 50 MPa, more preferably 20 to 45 MPa, and even more preferably 25 to 35 MPa.
- the MD tensile strength is 20 MPa or more, it is possible to prevent the film from breaking in the processing process. Further, when the MD tensile strength is 50 MPa or less, a PTP lid material having good protrusionability can be obtained.
- Examples of the method for controlling the MD tensile strength of the PTP lid material include a method of changing the crystallinity of the resin and stretching, and the MD tensile strength tends to increase when the crystallinity is increased or stretched. It is in.
- the TD tensile strength of the PTP lid material of the present embodiment is preferably 20 to 50 MPa, more preferably 20 to 45 MPa, and even more preferably 25 to 35 MPa.
- the TD tensile strength is 20 MPa or more, it is possible to prevent the film from breaking in the processing process. Further, when the TD tensile strength is 50 MPa or less, a PTP lid material having good protrusionability can be obtained.
- Examples of the method for controlling the TD tensile strength of the PTP lid material include a method of changing the crystallinity of the resin and stretching, and when the crystallinity is increased or stretched, the MD tensile strength tends to increase. It is in.
- the tensile strengths of MD and TD can be measured in accordance with JIS K7127, and specifically, can be measured by the method described in Examples described later.
- the MD tensile elongation of the PTP lid material of the present embodiment is preferably 15% or less, more preferably 11% or less, still more preferably 9% or less.
- the protrusion property in the TD direction tends to be good (the lid material tends to be easily pierced in a state where the crack enters the TD direction).
- the method for controlling the MD tensile elongation of the PTP lid material include a method of adjusting the crystallinity, MD orientation degree, fracture starting point, vulnerability, breaking strength, etc. of the PTP lid material.
- the fragility is increased by increasing the ratio of the fragile layer such as the resin layer, and the breaking strength is decreased by softening the fragile layer.
- the TD tensile elongation of the PTP lid material of the present embodiment is preferably 15% or less, more preferably 11% or less, still more preferably 9% or less.
- the protrusion property in the MD direction tends to be good (the lid material is likely to be pierced in a state where the crack enters the MD direction).
- Examples of the method for controlling the TD tensile elongation of the PTP lid material include a method of adjusting the crystallinity, the TD orientation degree, the fracture starting point, the brittleness, the fracture strength and the like of the PTP lid material.
- TD tensile elongation
- increase the crystallinity of the lid material for PTP decrease the degree of orientation of TD, increase the starting point of fracture by adding an inorganic substance, etc., and the above-mentioned low molecular weight polypropylene system.
- the fragility is increased by increasing the ratio of the fragile layer such as the resin layer, and the breaking strength is decreased by softening the fragile layer.
- the tensile elongation of MD and TD can be measured according to JIS K7127, and specifically, can be measured by the method described in Examples described later.
- the MD tensile elastic modulus of the PTP lid material of the present embodiment is preferably 300 to 1500 MPa, more preferably 400 to 1400 MPa, and further preferably 600 to 1200 MPa.
- the MD tensile elastic modulus is 300 MPa or more, the film is suppressed from stretching when printing on the PTP lid material, and printing misalignment can be prevented.
- the MD tensile elastic modulus is 1500 MPa or less, it is possible to suppress the PTP lid material from becoming hard and prevent cracking during processing.
- Examples of the method for controlling the MD tensile elastic modulus of the PTP lid material include a method of adjusting the crystallization degree and the MD orientation degree of the PTP lid material. When the crystallization degree and the MD orientation degree are lowered, the MD tension is used. The elastic modulus tends to decrease.
- the TD tensile elastic modulus of the PTP lid material of the present embodiment is preferably 1500 MPa or less, more preferably 1400 MPa or less, and further preferably 1200 MPa or less.
- the method for controlling the TD tensile elastic modulus of the PTP lid material include a method of adjusting the crystallization degree and the MD orientation degree of the PTP lid material. When the crystallization degree and the MD orientation degree are lowered, the TD tension The elastic modulus tends to decrease.
- the tensile elastic modulus of MD and TD can be measured according to JIS K7127, and specifically, can be measured by the method described in Examples described later.
- the amount of heat of crystal melting measured by the differential scanning calorimetry (DSC) of the lid material for PTP of the present embodiment is 70 J / g or more, preferably 75 to 200 J / g, and more preferably 80 to 200 J / g. be.
- the amount of heat for melting the crystal is in the above range, the MD and TD tensile elongations and the piercing elongations are suitable, and tend to show good ejection properties.
- Examples of the method for controlling the amount of heat of crystal melting of the PTP lid material include a method of adjusting cooling of the lid material during production of the PTP lid material, annealing after production, addition of a crystal nucleating agent, and the like.
- DSC differential scanning calorimeter
- the crystallinity measured by the Fourier transform infrared spectrophotometer (FT-IR) of the lid material for PTP of the present embodiment is preferably 46% or more, more preferably 47% or more, still more preferably. It is over 48%.
- the method for controlling the crystallinity of the PTP lid material include a method of adjusting the cooling of the lid material at the time of producing the PTP lid material, annealing after production, addition of a crystal nucleating agent, and the like.
- the lid material for PTP is manufactured by the direct inflation method
- the cooling of the lid material by airing is gradually cooled
- the lid material is annealed after the manufacture, and a crystal nucleating agent is added to crystallize.
- the degree of crystallinity can be increased.
- the crystallinity by FT-IR can be specifically measured by the method described in Examples described later, and can be similarly measured by using a Raman spectrophotometer.
- the MD orientation of the PTP lid material of the present embodiment is preferably ⁇ 0.035 to 0.035, more preferably ⁇ 0.03 to 0.03, and even more preferably ⁇ 0.02 to 0.02 to 0.02 to 0.03. It is 0.02.
- the MD orientation degree is in the above range, the MD tensile elongation and the TD tensile elongation are likely to be in the preferable range, the balance between the MD and TD tensile elongations is excellent, and good protrusionability is exhibited.
- Examples of the method for controlling the MD orientation of the PTP lid material include a method of adjusting the cooling of the lid material, the TD stretching ratio (BUR), the timing, and the like when manufacturing the PTP lid material.
- the degree of MD orientation can be reduced.
- the degree of MD orientation can be measured using FT-IR, and specifically, it can be measured by the method described in Examples described later. Further, since the degree of MD orientation indicates the orientation toward MD with respect to TD, it may be calculated from the results of measuring the orientation toward MD with respect to the thickness direction and the orientation toward TD with respect to the thickness direction of the PTP lid material. ..
- the thickest layer tends to affect the characteristics of the PTP lid material, so that the thickest layer (if there are a plurality of thickest layers, the thickest layer). Either) may be measured. Further, the MD orientation degree can be measured by using a Raman spectrophotometer as in the case of using FT-IR.
- the maximum load decrease per 0.1 mm displacement in the fracture region is preferably 3 to 20 N, more preferably 4 to 18 N, still more preferably 5. It is ⁇ 15N.
- the PTP lid material having a maximum load reduction of more than 20 N per 0.1 mm displacement shows that the contents such as tablets are not easily torn when the contents such as tablets are taken out from the PTP package, and the sticking property tends to be poor.
- the maximum load decrease per 0.1 mm displacement is one of the factors most affecting the open recognition, and when the maximum load decrease per 0.1 mm displacement is less than 3N, the lid material for PTP is brittle.
- FIG. 2 shows an example of a load-displacement curve obtained when a puncture test is performed on the PTP lid material of the present embodiment.
- the maximum load reduction per displacement of 0.1 mm is 8N.
- the method for controlling the maximum load reduction per 0.1 mm displacement of the PTP lid material include a method of adjusting the weight average molecular weight of the polypropylene-based resin, the thickness of the PTP-based lid material, and the reinforcing layer.
- the maximum load reduction per 0.1 mm of displacement can be increased.
- the maximum load decrease per 0.1 mm of displacement in the fracture region of the load-displacement curve can be measured by the method described in Examples described later.
- the puncture strength of the PTP lid material of the present embodiment is preferably 6 to 15N, more preferably 7 to 13N, and even more preferably 8 to 10N.
- the piercing strength is 6 N or more, it is possible to prevent the PTP lid material from being torn by an external force during transportation of the PTP package. Further, when the piercing strength is 15 N or less, a PTP lid material having excellent protrusionability can be obtained.
- Examples of the method for controlling the puncture strength of the PTP lid material include a method of adjusting the weight average molecular weight of the polypropylene resin, the thickness of the PTP lid material, and the reinforcing layer, and the weight average molecular weight of the polypropylene resin and the PTP lid. Increasing the thickness of the material or providing a reinforcing layer tends to increase the puncture strength.
- the puncture strength is a value converted into a thickness of 40 ⁇ m, and can be specifically obtained by the method described in Examples described later.
- the piercing elongation of the PTP lid material of the present embodiment is preferably 1 to 4 mm, more preferably 1.2 to 3 mm, still more preferably 1.5 to 2.5 mm.
- the piercing elongation is 1 mm or more, it is possible to prevent the PTP lid material from being torn by an external force during transportation of the PTP package.
- the piercing elongation is one of the factors having the greatest influence on the protruding property as well as the tensile elongation and the protruding strength, and when the piercing elongation is 4 mm or less, the PTP lid material having excellent protruding property is obtained. Can be obtained.
- Examples of the method for controlling the piercing elongation of the PTP lid material include a method of adjusting the weight average molecular weight of the polypropylene resin, the layer ratio of the PTP lid material, the degree of crystallization, the degree of MD and TD orientation, and the like.
- the weight average molecular weight of the polypropylene resin is reduced, the proportion of the low molecular weight polypropylene resin is increased, the degree of crystallization is increased, or the degree of MD and TD orientation is decreased, the puncture elongation tends to decrease. be.
- the puncture elongation can be measured by the method described in Examples described later.
- the method for producing the lid material for PTP is not particularly limited, but as an example, direct inflation in which the constituent material is extruded into a tube shape using a known melt extruder equipped with an annular die and then directly blown with air for stretching. The law is mentioned.
- the lid material for PTP is a laminated body composed of a plurality of layers
- the coextrusion direct inflation method is preferable.
- a method for manufacturing the PTP lid material, which is a laminated body, by the coextrusion direct inflation method will be described in outline.
- the resin or resin composition that is the constituent material of each layer is melted at a temperature higher than the melting temperature of the resin, and each layer is extruded at the same time using the number of extruders corresponding to the number of layers.
- the extruded resin or resin composition of each layer is sent to an annular die through a feed pipe to prepare a tubular film in which each layer is laminated via the annular die. Subsequently, air (air, nitrogen, etc.) is blown into the film to form bubbles, and the film is stretched in the MD and TD directions to manufacture a lid material for PTP.
- the MD stretch ratio (DDR) of the film is preferably 8 to 23 times, more preferably 10 to 20 times.
- the MD stretching ratio is 8 times or more, the pulsation of the bubble is suppressed and the stretching tends to be stabilized.
- the MD draw ratio is 23 times or less, a lid material having a suitable MD orientation degree, an excellent balance between the MD and TD orientation degrees, and a good protrusion property can be obtained.
- the TD stretch ratio (BUR) of the film is preferably 1.3 to 4 times, more preferably 1.5 to 2.5 times. When the TD stretching ratio is 1.3 times or more, the MD orientation degree is suitable, the balance between the MD and TD orientation degree is excellent, and a lid material showing good protrusion property can be obtained.
- the MD draw ratio can be adjusted by the speed of the pinch roller, and the TD draw ratio can be adjusted by the volume of air blown into the film.
- the stretching temperature of the film is preferably 70 to 160 ° C, more preferably 80 to 120 ° C.
- the stretching temperature is the temperature measured by a non-contact thermometer on the film surface at a portion vertically 32 cm away from the ejection surface of the annular die on the downstream side of the manufacturing process, and is the wind speed of the air ring for cooling the molten resin. It can be adjusted by the discharge amount of the molten resin, DDR and the like.
- FIG. 1 is a cross-sectional view showing an example of a PTP package provided with the PTP lid material of the present embodiment.
- the PTP package 1 includes a PTP lid material 2 and a bottom material 3.
- the bottom material 3 has a pocket-shaped recess 4 and a flange portion 5 bonded to the lid material 2, and the recess 4 is filled with the contents 6.
- Examples of the bottom material constituting the PTP package of the present embodiment include a polyvinyl chloride resin, a polyvinylidene chloride resin, and a polyolefin resin (for example, a polyethylene resin, a polypropylene resin, and an ethylene-vinyl alcohol copolymer resin). , Cyclic olefin resin, etc.), polychlorotrifluoroethylene, polyester and other well-known synthetic resins, and preferred are sheet materials made of these synthetic resins.
- a polyethylene resin a polypropylene resin, and a cyclic olefin resin
- a polypropylene resin as in the case of the lid material for PTP.
- the bottom material preferably has a heat distortion temperature of 50 to 160 ° C., preferably 80 to 120 ° C., in accordance with JIS K7191 from the viewpoint of a wide range of molding conditions for vacuum or pneumatic molding the pocket-shaped recesses of the bottom material. Is more preferable.
- the shape of the bottom material is not particularly limited as long as it has a recess for accommodating the contents, and the shape of the bottom surface portion and the opening portion of the recess is rectangular (square, rectangle, triangle, etc.) or circular (circle, ellipse, etc.). ), And the rectangle may have rounded corners.
- the size of the bottom material is not particularly limited and may be appropriately determined according to the size and number of the contents.
- the depth of the recess may be 1 to 15 mm, preferably 2 to 10 mm. ..
- the diameter of the opening portion may be, for example, 5 to 150 mm, preferably 10 to 100 mm, respectively, and the diameter of the bottom surface portion is set. Each may be 5 to 20% smaller than the diameter of the opening.
- the flange portion which is a portion other than the concave portion is not particularly limited, but may be provided so as to extend in a direction orthogonal to the depth direction of the concave portion.
- the average width of the flange portion may be, for example, 2 to 100 mm, preferably 4 to 50 mm.
- the thickness of the bottom material 1 is not particularly limited, and may be, for example, 100 to 500 ⁇ m, preferably 150 to 300 ⁇ m.
- the PTP package of the present embodiment can be manufactured by superimposing the surface of the bottom material (flange portion) and the surface of the lid material and heat-sealing them.
- the heat seal temperature is, for example, 100 to 160 ° C., and is preferably 100 to 140 ° C. from the viewpoint of making it difficult for the contents to be burnt.
- the heat sealing time is, for example, 0.05 to 3 seconds, and is preferably 0.2 to 1 second from the viewpoint that the contents are less likely to be burnt and a sufficient sealing strength can be obtained.
- the heat-sealing pressure is, for example, 0.2 to 0.6 MPa, and is preferably 0.3 to 0.5 MPa from the viewpoint of preventing burn marks on the contents and obtaining sufficient sealing strength.
- a roll seal molding machine in which a lid material and a bottom material are sandwiched between a heat seal roll and a roll under the seal to perform heat sealing, and heating of flat plates up and down.
- a flat seal molding machine having a mold and sandwiching a lid material and a bottom material with a mold for molding. Above all, it is preferable to use a flat seal molding machine that can easily obtain sufficient seal strength.
- TPO Polyolefin-based elastomer
- Toughmer XM7070 Polyolefin-based elastomer
- Adhesive resin > -Acid-modified polyolefin composition (manufactured by Mitsui Chemicals, Inc., Admar NF587)
- ⁇ Bottom material> -PP Polypropylene single-layer sheet (Sumilite NS-3450 (thickness 300 ⁇ m) manufactured by Sumitomo Bakelite Co., Ltd.). It was formed into a bottom material having a depth: 4 mm, an opening portion: a circle having a diameter of 10 mm, and a bottom portion: a circular recess having a diameter of 8 mm, and having a flange portion having an average width of 10 mm extending in a direction orthogonal to the depth direction.
- the opening portions were arranged in columns and rows orthogonal to each other, and the distance between the centers of the opening portions was 20 mm in the vertical direction and 20 mm in the horizontal direction.
- -PP / PE Polypropylene (manufactured by SunAllomer Ltd., PL500A), polypropylene (manufactured by SunAllomer Ltd., PC540R), polyethylene (manufactured by Ube-Maruzen Polyethylene Co., Ltd., Ube-Maruzen Polyethylene Co., Ltd., Umerit 0520F) by the coextrusion direct inflation method.
- a laminated multilayer sheet having a thickness of 300 ⁇ m was produced. The polyethylene side of the multilayer sheet was used as a heat-sealing surface, and molding was performed in the same manner as the polypropylene single-layer sheet described above.
- -PVC Polyvinyl chloride single layer sheet (Sumilite VSS-F110 (thickness 250 ⁇ m) manufactured by Sumitomo Bakelite Co., Ltd.). It was molded in the same manner as the polypropylene single layer sheet described above.
- Weight average molecular weight With respect to the polypropylene-based resin used as the lid material for PTP in Examples and Comparative Examples, the weight average molecular weight was measured by the following procedure. First, 1,2,4-trichlorobenzene was added to the sample so that the concentration became 1 mg / mL, and the sample was allowed to stand at 160 ° C. for 30 minutes and then shaken at 160 ° C. for 1 hour to dissolve. The solution was filtered through a 0.5 ⁇ m PTFE filter, and the polystyrene-equivalent weight average molecular weight was measured with GPC (PL-GPC220, manufactured by Agilent). The column used for the measurement was a combination of two TSK-gelGMH HR -H (20) HT (7.8 mm ⁇ 30 cm) manufactured by Tosoh Corporation, and the column temperature was 160 ° C.
- the movement was performed at a moving speed of 200 mm / min between the chucks, and at that time, the maximum load and the maximum elongation required for breaking were measured and used as the tensile strength (MPa) and the tensile elongation (%), respectively. Further, the load at the time of 2% elongation was defined as the tensile elastic modulus (MPa). The values measured for 10 test pieces were averaged and used as the tensile strength, tensile elongation, and tensile elastic modulus of the PTP lid material.
- Crystallinity The crystallinity (%) of the PTP lids obtained in Examples and Comparative Examples was measured using a Fourier transform infrared spectrophotometer (FT / IR4100, manufactured by JASCO Corporation). did. To calculate the crystallinity, the absorbance of polypropylene resin 973 cm -1 (peak derived from crystals and amorphous) and 998 cm -1 (peak derived from crystals) (hereinafter, the absorbance indicates the height of the peak). was calculated by the following formula.
- Crystallinity 0.56 x Absorbance (998 cm -1 ) / Absorbance (973 cm -1 ) x 100 The number of integrations during measurement was 16 times, the resolution was 4 cm -1 , and the average value of the values measured for 5 test pieces was taken as the crystallinity.
- MD orientation of the PTP lid materials obtained in Examples and Comparative Examples was measured using a Fourier transform infrared spectrophotometer (FT / IR4100, manufactured by JASCO Corporation).
- the degree of MD orientation was determined by the following formula using the absorbance of 973 cm -1 of each polypropylene resin measured at 0 ° (MD) and 90 ° (TD) of the grid splitter for the PTP lid material. rice field.
- the number of integrations during measurement was 16 times, the resolution was 4 cm -1 , and the average value of the values measured for 5 test pieces was taken as the MD orientation degree.
- Puncture strength and piercing elongation were measured by the following procedure.
- the lid material for PTP was fixed in a state of being stretched on a frame having a diameter of 10 mm.
- a puncture test was performed by attaching a needle with a diameter of 4 mm and a flat tip to a precision universal testing machine (manufactured by Shimadzu Corporation, Autograph) and pushing it into a fixed PTP lid material.
- the measurement was performed in an environment of a temperature of 23 ° C. and a humidity of 50% RH, and the moving speed of the needle was 50 mm / min.
- the maximum load applied to the needle at the time of tearing was defined as the puncture strength (N) and converted into a thickness of 40 ⁇ m. Further, the depth of the position of the tip of the needle at the time of occurrence of tear (displacement from the contact of the needle with the fixed PTP lid material to the position at the time of occurrence of tear) was defined as the puncture elongation (mm). The values measured for the five test pieces were averaged and used as the puncture strength and puncture elongation of the PTP lid material.
- the load reduction at break in the piercing test was measured by the following procedure.
- the lid material for PTP was fixed in a state of being stretched on a frame having a diameter of 10 mm.
- a puncture test was performed by attaching a needle with a diameter of 4 mm and a flat tip to a precision universal testing machine (manufactured by Shimadzu Corporation, Autograph) and pushing it into a fixed PTP lid material.
- the measurement was performed in an environment of a temperature of 23 ° C. and a humidity of 50% RH, and the moving speed of the needle was 50 mm / min.
- this test piece was attached so that a seal portion was placed between the chucks of a precision universal testing machine (manufactured by Shimadzu Corporation, Autograph) and the distance between the chucks was 30 mm. The movement was performed at a moving speed of 200 mm / min between the chucks, a 180 ° peeling test was carried out, and the maximum load until the sealed portion was completely peeled was defined as the sealing strength (N / 15 mm). The values measured for 10 test pieces were averaged and used as the sealing strength of the PTP lid material.
- Opening recognition For the PTP packages obtained in Examples and Comparative Examples, the opening sound when the contents were taken out by breaking through the lid material was recorded using a normal sound level meter (NA-29, manufactured by Rion Co., Ltd.). The opening recognition was evaluated according to the following evaluation criteria. At the time of opening sound measurement, the distance between the tip of the microphone and the lid material to break through was set to 30 mm, and the average value of 10 measurements was adopted. [Evaluation criteria] ⁇ (excellent): 80 dB or more ⁇ (good): 60 dB or more, less than 80 dB ⁇ (defective): less than 60 dB, or it is impossible to break through the lid material
- the gas adsorbed on the activated carbon-based adsorbent was desorbed at 300 ° C. in the TDU section using a heat desorption device (TDU2 manufactured by Gestel) installed in the GC / MS injection port. During that time, the gas was reconcentrated at ⁇ 40 ° C. in the CIS section and heated again to 300 ° C. for GC / MS measurement.
- the unpleasant odor components of the lid material for PTP include acetic acid, butanoic acid, acetylacetone and the like, and the film odor was evaluated as follows based on the detected amounts of butanoic acid and acetic acid.
- Example 1 Using the coextrusion direct inflation method, a two-layer PTP lid material in which a polypropylene resin (PP) layer (first layer) and a polyolefin-based elastomer (TPO) layer (second layer) were laminated was produced. Specifically, the pellets of the resin, which is the raw material of each layer, were melted at a temperature equal to or higher than the melting temperature of the resin, and each layer was extruded at the same time using a plurality of extruders. The extruded resin of each layer was sent to an annular die through a feed pipe, and a tubular laminated film in which each layer was laminated was produced through the annular die.
- PP polypropylene resin
- TPO polyolefin-based elastomer
- the stretching ratio was MD30 times and TD2 times, and the stretching temperature was 61 ° C.
- a tablet is filled in the recess of the PP bottom material, and the PP bottom material and the lid material (TPO layer side) are adhered by heat sealing using an Acein pack sealer (manufactured by Acein pack industry, semi-automatic OS) to form a PTP package.
- Got The conditions for heat sealing were a temperature of 140 ° C., a pressure of 0.4 MPa, and a time of 1 second. Table 1 shows the measurement / evaluation results of each physical property.
- Example 2 to 5 and Comparative Examples 1 to 3 PTP lids were prepared in the same manner as in Example 1 except that the raw materials, blending amounts, etc. were changed as shown in Table 1, and PTP packages were obtained. rice field.
- amorphous aluminosilicate was mixed with polypropylene resin (PP2) before extrusion.
- Table 1 shows the detailed conditions and the measurement / evaluation results of each physical property.
- Example 6 In Example 6, as shown in Table 1, the raw materials, the blending amount, and the like were changed to prepare a two-layer film in which the first layer and the second layer were laminated in the same manner as in Example 1, and then the first layer was prepared.
- a lid material for PTP was produced by corona treating the side surface and providing an inorganic vapor deposition layer (third layer) of aluminum by a vacuum vapor deposition method at 10 nm.
- the PP bottom material and the lid material (TPO layer side) were adhered in the same manner as in Example 1 to obtain a PTP package.
- Table 1 shows the detailed conditions and the measurement / evaluation results of each physical property.
- Comparative Example 4 In Comparative Example 4, as shown in Table 1, the raw materials, the blending amount, and the like were changed to prepare a two-layer film in which the first layer and the second layer were laminated in the same manner as in Example 1, and then Patent Document 1 A lid material for PTP was produced by irradiating an electron beam having an acceleration voltage of 250 kV and an irradiation dose of 60 kGy with reference to. The PP / PE bottom material (PE layer side) and the lid material (PE layer side) were adhered in the same manner as in Example 1 to obtain a PTP package. Table 1 shows the detailed conditions and the measurement / evaluation results of each physical property.
- EVA ethylene vinyl acetate
- the PP bottom material and the lid material (TPO layer side) were adhered in the same manner as in Example 1 to obtain a PTP package.
- Table 1 shows the detailed conditions and the measurement / evaluation results of each physical property.
- the lid material for a PTP package of the present invention can be suitably used for packaging pharmaceutical products such as tablets and capsules and food products such as candy and chocolate.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Composite Materials (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Wrappers (AREA)
- Laminated Bodies (AREA)
- Packages (AREA)
Abstract
Description
また、特許文献2および3には、ポリプロピレン系樹脂と、突き出し性を向上させるための無機物(タルク等)とを含む樹脂組成物からなるシートを基材とするPTP用蓋材が開示されている。
特許文献4には、底材と同じ条件で処理できる易焼却性を有し、優れた引張切断荷重、伸び及び易突き破り性を発現させるため、結晶性熱可塑性樹脂を必須成分とし、熱処理により結晶化させたブリスターパック包装体の蓋材用シートが開示されている。
特許文献5には、手切れ性、機械的強度等に加え、層間接着力を向上させるため、層間部に一定範囲の結晶融解熱量を有する樹脂を積層した積層ポリプロピレン系フィルムが開示されている。
特許文献6には、使用後の廃棄処理を容易にし、プレススルー性及び印刷判読性を向上させるため、スチレン系樹脂と無機フィラーを使用したプラスチック製PTP用蓋材フィルム及びこれを用いたPTP包装体が開示されている。
また、特許文献2および3に記載された蓋材は、いずれも、蓋材を突き破って内容物を取り出す際に開封音が発生することによる開封認識性の点で、更なる改良の余地がある。
特許文献4に記載された蓋材は、上述の開封認識性の点で改良の余地があることに加え、ポリスチレン、エチレン-酢酸ビニル共重合体ケン化物およびナイロン-6などの異なる樹脂を積層しているため、マテリアルリサイクルに不向きという問題がある。
特許文献5に記載された蓋材には、二軸配向ポリプロピレン系樹脂を積層しているため、突き出し性や開封認識性が悪化するという問題がある。
特許文献6に記載された蓋材には、スチレン系樹脂が使用されているため、リサイクルに不向きである上、エマルジョン型ヒートシール剤が塗布されているため、高温環境下で不快な臭気が発生するという問題がある。
[1]
重量平均分子量が2.0×105~3.5×105であるポリプロピレン系樹脂を含み、示差走査熱量計(DSC)による結晶融解熱量が70J/g以上であることを特徴とする、PTP用蓋材。
[2]
MD配向度が-0.035~0.035である、[1]に記載のPTP用蓋材。
[3]
前記PTP用蓋材の突刺試験時の荷重-変位曲線において、破断領域における変位0.1mmあたりの最大荷重低下が3~20Nである、[1]または[2]に記載のPTP用蓋材。
[4]
厚みが10~100μmであり、水蒸気透過度が10g/m2・day以下であり、引張強度がMDおよびTDいずれも20~50MPaであり、かつ引張伸度がMDおよびTDいずれも15%以下である、[1]~[3]のいずれかに記載のPTP用蓋材。
[5]
無機物を0.1~3質量%含む、[1]~[4]のいずれかに記載のPTP用蓋材。
[6]
前記ポリプロピレン系樹脂を含む層と、ポリエチレン系樹脂、ポリプロピレン系樹脂、またはポリオレフィン系エラストマーを含む少なくとも1つの表層とを含む、[1]~[5]のいずれかに記載のPTP用蓋材。
[7]
[1]~[6]のいずれかに記載のPTP用蓋材と、内容物を収容する凹部を有する底材とを含むことを特徴とする、PTP包装体。
本実施形態のPTP用蓋材(以下、単に「蓋材」ともいう。)は、重量平均分子量が2.0×105~3.5×105であるポリプロピレン系樹脂を含み、かつ示差走査熱量計(DSC)による結晶融解熱量が70J/g以上であることを特徴とする。
本実施形態のPTP用蓋材に含まれるポリプロピレン系樹脂は、重量平均分子量が2.0×105~3.5×105であれば、特に限定されることなく、例えば、プロピレンホモポリマー、プロピレンと他のモノマーとの共重合体、およびこれらの変性物等が挙げられる。また、環境対応の観点から、バイオポリプロピレンであってもよい。中でも、耐熱性、水蒸気バリア性、引張伸度の観点から、プロピレンホモポリマーが好ましい。
ポリプロピレン系樹脂は、1種単独でも、2種以上を組み合わせて併用してもよい。
上記触媒としては、三塩化チタン触媒、塩化マグネシウム等の担体に担持したハロゲン化チタン触媒等が挙げられる。重合体の分子量を調整するために、水素等の連鎖移動剤を添加してもよい。
変性ポリプロピレン系樹脂は、例えば、ラジカル発生剤の存在下または非存在下、溶融状態、溶液状態、またはスラリー状態で、30~350℃の範囲で、未変性のポリプロピレン系樹脂と変性剤とを反応させることによって得られる。
なお、重量平均分子量は、ゲルパーミエーションクロマトグラフィー(以下、「GPC」ともいう。)を用いて測定することができ、具体的には、後述の実施例に記載の方法により測定することができる。
低分子量ポリプロピレン系樹脂層に積層するその他の層としては、例えば、PTP用底材とのシール性を向上させるためのシール層、強度や突き出し性等の蓋材の物性を調整するための調整層、包装時のフィルム切れを防止するための補強層、ガスバリア性を向上させるためのバリア層等が挙げられる。
積層数は、特に限定されないが、強度、突き出し性、水蒸気バリア性、シール性、およびリサイクル性のバランスの観点から、2~5層であることが好ましく、2~3層であることがより好ましい。
当該表層は、底材に接着される底材側の表層および外側の表層(最外層)のいずれか一方であっても、両方であってもよい。例えば、包装時のフィルム切れを防止するための補強層として外側の表層であってもよい。また、ポリエチレン系樹脂、ポリプロピレン系樹脂、またはポリオレフィン系エラストマーを含むことにより、ヒートシール性に優れるとともに、これらの樹脂は共押出可能なため、エマルジョン型ヒートシール剤の塗布が不要となり、高温環境下でも不快な臭気が発生しないことから、底材に接着される底材側の表層として好適である。中でも、特に低温シール性に優れることから、ポリオレフィン系エラストマーを含む層であることが好ましく、リサイクル性の観点からは、PTP用蓋材全体がポリプロピレン系樹脂で構成されるように、ポリプロピレン系樹脂を含む層であることが好ましい。
当該表層の厚みは、PTP用蓋材全体の厚みを100%として、5~40%であることが好ましく、より好ましくは5~30%であり、更に好ましくは10~25%である。表層の厚みが上記範囲であると、突き出し性を悪化させることなく良好なヒートシール性を付与したり、フィルム切れを防止することができる。
ポリプロピレン系樹脂の分子量は、特に限定されないが、上述の低分子量ポリプロピレン系樹脂層に含まれるポリプロピレン系樹脂よりも高いことが好ましい。例えば、メルトフローレート(MFR、ASTM D-1238に準拠して230℃、2.16kgfの荷重で測定)が3~15g/10分であるものが挙げられる。
ポリプロピレン系樹脂は、1種単独でも、2種以上を組み合わせて併用してもよい。
中でも、低温シール性に優れることから、低融点(55~90℃)のポリプロピレン系エラストマーが好ましい。また、環境対応の観点から、バイオポリオレフィン系エラストマーであってもよい。更に、ポリオレフィン系エラストマーは、1種単独でも、2種以上を組み合わせて併用してもよい。
当該調整層の厚みは、PTP用蓋材全体の厚みを100%として、10~40%であることが好ましく、より好ましくは15~35%であり、更に好ましくは20~30%である。
ポリプロピレン系樹脂の種類としては、上述の低分子量のポリプロピレン系樹脂と同様のものが挙げられる。
ポリプロピレン系樹脂の分子量は、特に限定されないが、上述の低分子量ポリプロピレン系樹脂層に含まれるポリプロピレン系樹脂よりも高いことが好ましい。例えば、メルトフローレート(MFR、ASTM D-1238に準拠して230℃、2.16kgfの荷重で測定)が3~15g/10分であるものが挙げられる。
ポリプロピレン系樹脂は、1種単独でも、2種以上を組み合わせて併用してもよい。
本実施形態のPTP用蓋材は、破断起点を増加させ、突き出し性を向上させるために、無機物を含んでいてもよい。
無機物は、特に限定されず、例えば、非晶質アルミナ珪酸塩、シリカ、アルミナ、タルク、カオリン、マイカ、ワラストナイト、クレー、炭酸カルシウム、ガラス繊維、硫酸アルミニウム等が挙げられる。
また、本実施形態のPTP用蓋材は、印刷の特性改善を目的としたコロナ処理、プラズマ処理、紫外線処理、AC(アンカーコート)処理等の処理を行ってもよい。
特に、白色の着色剤や印刷は、下記の理由から好ましい。近年、医薬品用のPTP包装体では、従来の製品名称ロゴや使用方法を示す図柄の他に、医療事故の防止やトレーザビリティーの確保を目的とした商品コード、有効期限、製造番号、数量といった各種情報を含んだバーコードを印刷することのニーズが高まりつつある。白色の着色剤を配合した蓋材や白色印刷したものを用いると、バーコードの読取りの際、線のない部分(蓋材が直接見える部分)が白いために、バーコードの線のある部分(一般的には黒色)との色の濃淡ができ、バーコードが読み取りやすくなる。
添加剤の含有量は、PTP用蓋材を100質量%として、3質量%以下であることが好ましい。
PTP用蓋材の水蒸気透過度は、例えば、PTP用蓋材の厚み、樹脂の種類の選択、バリア層の有無等により調整することができる。PTP用蓋材の厚みを厚くしたり、バリア層を設けることにより、水蒸気透過度は低下する傾向にある。前記バリア層には、エチレン-ビニルアルコール共重合体、環状オレフィン等の樹脂層や、アルミニウム、酸化アルミニウム、酸化ケイ素等の無機蒸着層が挙げられる。また、結晶化度の高い樹脂を使用することにより、PTP用蓋材の水蒸気透過度を低下させることができる。
なお、水蒸気透過度は、JIS K7129に準拠して測定し、40μm厚みに換算した値であり、具体的には、後述の実施例に記載の方法により求めることができる。
PTP用蓋材のMD引張強度の制御方法としては、例えば、樹脂の結晶化度を変更したり、延伸する方法が挙げられ、結晶化度を高めたり、延伸すると、MD引張強度は増加する傾向にある。
PTP用蓋材のTD引張強度の制御方法としては、例えば、樹脂の結晶化度を変更したり、延伸する方法が挙げられ、結晶化度を高めたり、延伸すると、MD引張強度は増加する傾向にある。
PTP用蓋材のMD引張伸度の制御方法としては、例えば、PTP用蓋材の結晶化度、MD配向度、破断起点、脆弱性、破断強度等を調整する方法が挙げられる。MD引張伸度を低下させるには、PTP用蓋材の結晶化度を増加させること、MD配向度を低下させること、無機物を添加する等により破断起点を増加させること、上述の低分子量ポリプロピレン系樹脂層等の脆弱な層の比率を増加させる等により脆弱性を増加させること、脆弱な層を柔軟化する等により破断強度を低下させること等が挙げられる。
PTP用蓋材のTD引張伸度の制御方法としては、例えば、PTP用蓋材の結晶化度、TD配向度、破断起点、脆弱性、破断強度等を調整する方法が挙げられる。TD引張伸度を低下させるには、PTP用蓋材の結晶化度を増加させること、TD配向度を低下させること、無機物を添加する等により破断起点を増加させること、上述の低分子量ポリプロピレン系樹脂層等の脆弱な層の比率を増加させる等により脆弱性を増加させること、脆弱な層を柔軟化する等により破断強度を低下させること等が挙げられる。
PTP用蓋材のMD引張弾性率の制御方法としては、例えば、PTP用蓋材の結晶化度やMD配向度を調整する方法が挙げられ、結晶化度やMD配向度を低くすると、MD引張弾性率は低下する傾向にある。
PTP用蓋材のTD引張弾性率の制御方法としては、例えば、PTP用蓋材の結晶化度やMD配向度を調整する方法が挙げられ、結晶化度やMD配向度を低くすると、TD引張弾性率は低下する傾向にある。
PTP用蓋材の結晶融解熱量の制御方法としては、例えば、PTP用蓋材を製造する際の蓋材の冷却、製造後のアニール、結晶核剤の添加等を調整する方法が挙げられる。一例として、PTP用蓋材をダイレクトインフレーション法により製造する際の冷却を徐冷化すること、蓋材を製造後にアニールすること、結晶核剤を添加すること等により結晶融解熱量を増加させることができる。
なお、示差走査熱量計(DSC)による結晶融解熱量の測定は、具体的には、後述の実施例に記載の方法により行うことができる。
PTP用蓋材の結晶化度の制御方法としては、例えば、PTP用蓋材を製造する際の蓋材の冷却、製造後のアニール、結晶核剤の添加等を調整する方法が挙げられる。一例として、PTP用蓋材をダイレクトインフレーション法により製造する際にエアリングによる蓋材の冷却を徐冷化すること、蓋材を製造後にアニールすること、結晶核剤を添加すること等により、結晶化度を増加させることができる。
なお、FT-IRによる結晶化度の測定は、具体的には、後述の実施例に記載の方法により行うことができ、ラマン分光光度計を用いて同様に測定することも可能である。
PTP用蓋材のMD配向度の制御方法としては、例えば、PTP用蓋材を製造する際の蓋材の冷却、TD延伸の倍率(BUR)またはタイミング等を調整する方法が挙げられる。一例として、PTP用蓋材をダイレクトインフレーション法により製造する際にエアリングによる蓋材の冷却を徐冷化すること、TD延伸倍率(BUR)を増加させること、逐次二次延伸により製造すること等により、MD配向度を低下させることができる。
なお、MD配向度は、FT-IRを用いて測定することができ、具体的には、後述の実施例に記載の方法により測定することができる。
また、MD配向度はTDに対するMDへの配向を示していることから、PTP用蓋材の厚み方向に対するMDへの配向および厚み方向に対するTDへの配向をそれぞれ測定した結果から算出してもよい。その際、PTP用蓋材が多層構成である場合は、最も厚みの厚い層がPTP蓋材の特性に影響を与えやすいため、最も厚みの厚い層(最も厚みの厚い層が複数ある場合はそのいずれか)の配向度を測定すればよい。
また、MD配向度は、FT-IRを用いる場合と同様に、ラマン分光光度計を用いて測定することも可能である。
図2に、本実施形態のPTP用蓋材に対して突刺試験を実施した際に得られる荷重-変位曲線の一例を示す。図2のPTP用蓋材の場合、変位0.1mmあたりの最大荷重低下は8Nである。
PTP用蓋材の変位0.1mmあたりの最大荷重低下を制御する方法としては、例えば、ポリプロピレン系樹脂の重量平均分子量、PTP用蓋材の厚み、補強層を調整する方法が挙げられ、ポリプロピレン系樹脂の重量平均分子量やPTP蓋材の厚みを大きくしたり、補強層を設けると、変位0.1mmあたりの最大荷重低下を大きくすることができる。
なお、荷重-変位曲線の破断領域における変位0.1mmあたりの最大荷重低下は、具体的には、後述の実施例に記載の方法により測定することができる。
PTP用蓋材の突刺強度の制御方法としては、例えば、ポリプロピレン系樹脂の重量平均分子量、PTP用蓋材の厚み、補強層を調整する方法が挙げられ、ポリプロピレン系樹脂の重量平均分子量やPTP蓋材の厚みを大きくしたり、補強層を設けると、突刺強度は増加する傾向にある。
なお、突刺強度は、40μm厚みに換算した値であり、具体的には、後述の実施例に記載の方法により求めることができる。
PTP用蓋材の突刺伸度の制御方法としては、例えば、ポリプロピレン系樹脂の重量平均分子量、PTP用蓋材の層比率、結晶化度、MDおよびTD配向度等を調整する方法が挙げられ、ポリプロピレン系樹脂の重量平均分子量を小さくしたり、低分子量のポリプロピレン系樹脂の割合を上げたり、結晶化度を増加させたり、MDおよびTD配向度を減少させると、突刺伸度は低下する傾向にある。
なお、突刺伸度は、具体的には、後述の実施例に記載の方法により測定することができる。
PTP用蓋材の製造方法としては、特に限定されないが、一例として、環状ダイを備えた公知の溶融押出機を用いて上記構成材料をチューブ状に押出した後、直接エアーを吹き込み延伸させるダイレクトインフレーション法が挙げられる。PTP用蓋材が複数層からなる積層体である場合は、共押出ダイレクトインフレーション法であることが好ましい。
以下、積層体であるPTP用蓋材を共押出ダイレクトインフレーション法により製造する方法について、その概略を説明する。
また、フィルムのTD延伸倍率(BUR)は、1.3~4倍であることが好ましく、より好ましくは、1.5~2.5倍である。TD延伸倍率1.3倍以上であると、MD配向度が好適でMDおよびTD配向度のバランスに優れ、良好な突き出し性を示す蓋材が得られる。また、TD延伸倍率が4倍以下であると、バブルの脈動が抑制され、延伸が安定化する傾向にある。
なお、MD延伸倍率は、ピンチローラーの速度で調節することができ、TD延伸倍率は、フィルム内に吹き込むエアーの体積により調節することができる。
なお、延伸温度は、環状ダイの吐出表面から垂直に32cm製造工程下流側に離れた部分のフィルム表面を非接触温度計で実測した温度であり、溶融樹脂を冷却するためのエアリングの風速、溶融樹脂の吐出量、DDR等によって調整することができる。
本実施形態のPTP包装体は、上述の本実施形態のPTP用蓋材と、内容物を収容する凹部を有する底材とを含むことを特徴とする。
図1は、本実施形態のPTP用蓋材を備えたPTP包装体の一例を示す断面図である。PTP包装体1は、PTP用蓋材2と底材3とを備える。底材3は、ポケット状の凹部4と、蓋材2と貼り合わされるフランジ部5とを有し、凹部4には、内容物6が充填されている。
本実施形態のPTP包装体を構成する底材としては、例えば、ポリ塩化ビニル系樹脂、ポリ塩化ビニリデン系樹脂、ポリオレフィン系樹脂(例えば、ポリエチレン系樹脂、ポリプロピレン系樹脂、エチレン-ビニルアルコール共重合樹脂、環状オレフィン樹脂等)、ポリクロロトリフルオロエチレン、ポリエステル等の周知の合成樹脂を含むシート材が挙げられ、好適には、これらの合成樹脂からなるシート材である。中でも、リサイクル性の観点から、ポリエチレン系樹脂、ポリプロピレン系樹脂、環状オレフィン樹脂を含むことが好ましく、PTP用蓋材と同様に、ポリプロピレン系樹脂を含むことが最も好ましい。
フランジ部の平均幅としては、例えば、2~100mmであってよく、好ましくは4~50mmである。
本実施形態のPTP包装体は、底材の表面(フランジ部)と蓋材の表面とを重ね合わせてヒートシールすることにより、製造することができる。
ヒートシール温度は、例えば、100~160℃が挙げられ、内容物の焼け跡がつきにくくなる観点から、100~140℃が好ましい。また、ヒートシール時間は、例えば、0.05~3秒が挙げられ、内容物の焼け跡がつきにくくなり、十分なシール強度が得られる観点から、0.2~1秒が好ましい。また、ヒートシール圧力は、例えば、0.2~0.6MPaが挙げられ、内容物の焼け跡がつきにくくなり、十分なシール強度が得られる観点から、0.3~0.5MPaが好ましい。
〈ポリプロピレン系樹脂(PP)〉
・PP1:ポリプロピレン(サンアロマー(株)製、PLB00A、重量平均分子量:2.2×105)
・PP2:ポリプロピレン(サンアロマー(株)製、PLA00A、重量平均分子量:2.6×105)
・PP3:ポリプロピレン(サンアロマー(株)製、VS700A、重量平均分子量:3.8×105)
・PP4:ポリプロピレン(サンアロマー(株)製、PL500A、重量平均分子量:6.0×105)
・ポリエチレン(宇部丸善ポリエチレン(株)製、ユメリット0520F)
・プロピレン-α-オレフィンコポリマー(三井化学(株)製、タフマーXM7070)
・エチレン-酢酸ビニル共重合体ケン化物(三菱ケミカル(株)製、ソアノールDC3203)
・酸変性ポリオレフィン組成物(三井化学(株)製、アドマーNF587)
・ポリスチレン(PSジャパン(株)製、PSJ-ポリスチレンG9305)
・非晶質アルミノケイ酸塩(水澤化学工業(株)社製、シルトンJC-30)
・PP:ポリプロピレン単層シート(住友ベークライト(株)製スミライトNS-3450(厚さ300μm))。深さ:4mm、開口部分:直径10mmの円形、底面部分:直径8mmの円形の凹部を有し、深さ方向に直交する方向に延びる平均幅10mmのフランジ部を有する底材に成形した。開口部分は互いに直交する縦列および横列に並べられ、開口部分の中心間距離は、縦について20mm、横について20mmとした。
・PP/PE:共押出ダイレクトインフレーション法により、ポリプロピレン(サンアロマー(株)製、PL500A)、ポリプロピレン(サンアロマー(株)社製、PC540R)、ポリエチレン(宇部丸善ポリエチレン(株)製、ユメリット0520F)の順に積層した厚み300μmの多層シートを作製した。前記多層シートのポリエチレン側をヒートシール面として、上述のポリプロピレン単層シートと同様に成形した。
・PVC:ポリ塩化ビニル単層シート(住友ベークライト(株)製スミライトVSS-F110(厚さ250μm))。上述のポリプロピレン単層シートと同様に成形した。
実施例および比較例でPTP用蓋材に用いたポリプロピレン系樹脂について、以下の手順で重量平均分子量を測定した。
まず、濃度が1mg/mLになるように試料に1,2,4-トリクロロベンゼンを加え、160℃で30分静置した後、160℃で1時間揺動させて溶解させた。前記溶解液を0.5μmのPTFEフィルタでろ過し、GPC(Agilent社製、PL-GPC220)にてポリスチレン換算の重量平均分子量を測定した。なお、測定に使用したカラムは、東ソー(株)製TSK-gelGMHHR-H(20)HT(7.8mm×30cm)を2本連結したものであり、カラム温度は160℃とした。
実施例および比較例で得られたPTP用蓋材について、水蒸気透過率測定装置(MOCON社製、PERMATRAN-W Model398)を使用して水蒸気透過度を測定した。測定は、JIS K7129に準拠し、38℃、90%RHにて水蒸気透過度(g/m2・day)を測定し、40μm厚みに換算した。
実施例および比較例で得られたPTP用蓋材について、JIS K7127に準拠して、MDおよびTDそれぞれの引張強度、引張伸度、および引張弾性率を測定した。
PTP用蓋材から、短冊状の試験片(長さ150mm×幅10mm)を切り出した。この試験片の端部を、精密万能試験機(島津製作所製、オートグラフ)に、チャック間距離が50mmとなるように取り付けた。チャック間の移動速度200mm/分にて移動を行い、その際に破断に要するまでの最大荷重および最大伸度を測定し、それぞれ、引張強度(MPa)および引張伸度(%)とした。また、2%伸長時の荷重を引張弾性率(MPa)とした。10枚の試験片について測定した値を平均し、そのPTP用蓋材の引張強度、引張伸度、および引張弾性率とした。
実施例および比較例で得られたPTP用蓋材からサンプル(5~10mg)を切り出し、示差走査熱量計(DSC)(日立ハイテクサイエンス社製、DSC7000X)を用いて、窒素雰囲気下、熱量標準としてインジウムを使用して測定を行った。加熱プログラムとしては、サンプルを10℃/分の昇温速度で0℃から200℃まで昇温し、得られた熱流曲線の融解に起因する吸熱ピークに対して、高温側から外挿する直線をベースラインとして、結晶融解熱量(J/g)を求めた。なお、融解に起因する吸熱ピークが複数存在した場合は、各結晶融解熱量の合計をPTP用蓋材の結晶融解熱量とした。
実施例および比較例で得られたPTP用蓋材について、フーリエ変換赤外分光光度計(日本分光社製、FT/IR4100)を用いて、結晶化度(%)を測定した。結晶化度の算出には、ポリプロピレン系樹脂の973cm-1(結晶と非晶に由来するピーク)と998cm-1(結晶に由来するピーク)の吸光度(以下、吸光度はピークの高さを表す)を使用し、以下の式により求めた。
結晶化度=0.56×吸光度(998cm-1)/吸光度(973cm-1)×100
なお、測定時の積算回数は16回、分解能は4cm-1とし、5枚の試験片について測定した値の平均値を結晶化度とした。
実施例および比較例で得られたPTP用蓋材について、フーリエ変換赤外分光光度計(日本分光社製、FT/IR4100)を用いて、MD配向度を測定した。PTP用蓋材に対して、グリッド偏光子0°(MD)および90°(TD)で測定し、各ポリプロピレン系樹脂の973cm-1の吸光度を使用して、以下の式によりMD配向度を求めた。
二色比(R)=吸光度(MD)/吸光度(TD)
MD配向度=(R-1)/(R+2)×1.17
なお、測定時の積算回数は16回、分解能は4cm-1とし、5枚の試験片について測定した値の平均値をMD配向度とした。
実施例および比較例で得られたPTP用蓋材について、以下の手順で突刺強度および突刺伸度を測定した。
PTP用蓋材を、直径10mmの枠に張った状態で固定した。精密万能試験機(島津製作所製、オートグラフ)に、直径4mm、先端が平板状の針を装着し、固定したPTP用蓋材に押し込むことで、突刺試験を行った。測定は温度23℃、湿度50%RHの環境下で行い、針の移動速度は50mm/分とした。破れ発生時の針にかかる最大荷重を突刺強度(N)とし、40μm厚みに換算した。また、破れ発生時の針の先端の位置の深さ(針が固定したPTP用蓋材に接してから破れ発生時における位置までの変位)を突刺伸度(mm)とした。5枚の試験片について測定した値を平均し、そのPTP用蓋材の突刺強度および突刺伸度とした。
実施例および比較例で得られたPTP用蓋材について、以下の手順で突刺試験破断時の荷重低下を測定した。
PTP用蓋材を、直径10mmの枠に張った状態で固定した。精密万能試験機(島津製作所製、オートグラフ)に、直径4mm、先端が平板状の針を装着し、固定したPTP用蓋材に押し込むことで、突刺試験を行った。測定は温度23℃、湿度50%RHの環境下で行い、針の移動速度は50mm/分とした。得られた荷重-変位曲線の破断領域において(破れ発生に伴う荷重低下の内)、変位0.1mmあたりの荷重低下が最大となる値を求めた。5枚の試験片について測定した値を平均し、そのPTP用蓋材の変位0.1mmあたりの最大荷重低下とした。
実施例および比較例で得られたPTP用蓋材について、以下の手順でシール強度を測定した。
まず、PTP用蓋材および底材をヒートシールテスター(テスター産業社製)によりヒートシールした。その際のシール温度を140℃、シール時間を2秒、シール圧力を0.25MPaとした。その後、短冊状の試験片(PTP用蓋材および底材の長さ各40mm(計80mm)×幅15mm)を切り出した。この試験片の端部を、精密万能試験機(島津製作所製、オートグラフ)のチャック間にシール部が配置され、チャック間距離が30mmとなるように取り付けた。チャック間の移動速度200mm/分にて移動を行い、180°剥離試験を実施し、シール部が完全に剥がれるまでの最大荷重をシール強度(N/15mm)とした。10枚の試験片について測定した値を平均し、そのPTP用蓋材のシール強度とした。
実施例および比較例で得られたPTP用蓋材の突刺伸度、PTP包装体の蓋材を突き破った際の層間剥離の発生の有無を総合し、下記の評価基準にて、突き出し性を評価した。
[評価基準]
◎(優れる):突刺伸度が2.6mm未満であり、かつPTP包装体の蓋材を突き破った際に層間剥離および部分破断が発生しない。
○(良好):突刺伸度が2.6mm以上、3.2mm未満であり、かつPTP包装体の蓋材を突き破った際に層間剥離および部分破断が発生しない。
×(不良):突刺伸度が3.2mm以上、またはPTP包装体の蓋材を突き破った際に層間剥離または部分破断が発生する。
実施例および比較例で得られたPTP包装体について、蓋材を突き破って内容物を取り出した際の開封音を普通騒音計(リオン株式会社製、NA-29)を用いて測定し、下記の評価基準にて、開封認識性を評価した。開封音測定時は、マイクロホン先端部と突き破る蓋材の距離を30mmとし、10回の測定の平均値を採用した。
[評価基準]
◎(優れる):80dB以上
○(良好):60dB以上、80dB未満
×(不良):60dB未満、または蓋材を突き破ることが不可能である
実施例および比較例で得られたPTP用蓋材について、フィルム臭気の有無をダイナミックヘッドスペース-GC/MS(Gestels社製DHS、Agilent社製GC-7890 MSD-5977B)を用いて測定した。サンプル調製は、20mL容量のガラス瓶中に2gのPTP用蓋材を入れ、50℃で30分加熱した。その間、活性炭系吸着材(Agilent社製、Carbopack B/Carbopack X)に1950mLの窒素ガスを使用してPTP用蓋材に含まれる臭気成分を吸着させた。加熱終了後、GC/MS注入口に設置した加熱脱着装置(Gestel社製、TDU2)を使用して、前記活性炭系吸着材に吸着したガスをTDU部にて300℃で脱着させた。その間CIS部にてガスを-40℃で再濃縮し、再度300℃に加熱してGC/MS測定を行った。PTP用蓋材の不快な臭気成分には、酢酸、ブタン酸、アセチルアセトン等があり、ブタン酸及び酢酸の検出量を基準にして、下記の通りフィルム臭気を評価した。
[評価基準]
○(優れる):ブタン酸の検出量が0.01ppm未満、かつ酢酸の検出量が0.1ppm未満である。
×(不良):ブタン酸の検出量が0.01ppm以上、または酢酸の検出量が0.1ppm以上である。
共押出ダイレクトインフレーション法を用いて、ポリプロピレン樹脂(PP)層(第一層)とポリオレフィン系エラストマー(TPO)層(第二層)とを積層した2層のPTP用蓋材を作製した。
具体的には、各層の原材料である樹脂のペレットを、樹脂の融解温度以上で溶融し、複数台の押出機を用いて各層を同時に押出した。押出された各層の樹脂をフィードパイプを通じて環状ダイに送り、環状ダイを介して各層が積層したチューブ状の積層フィルムを作製した。なお、厚み比がPP層:TPO層=80:20となるように調整した。
続いて、積層フィルムに空気を吹き込んで延伸させることにより、厚み40μmのPTP用蓋材を得た。なお、延伸倍率は、MD30倍、TD2倍とし、延伸温度は61℃とした。
PP底材の凹部に錠剤を充填し、エーシンパックシーラー(エーシンパック工業社製、半自動OS)を用いてヒートシールによりPP底材と蓋材(TPO層側)とを接着して、PTP包装体を得た。
ヒートシールの条件は、温度140℃、圧力0.4MPa、時間1秒とした。
表1に各物性の測定・評価結果を示す。
実施例2~5、比較例1~3は、表1に示すように原料、配合量等を変更したこと以外は実施例1と同様にしてPTP用蓋材を作製し、PTP包装体を得た。
なお、実施例5の第一層は、押出前に、ポリプロピレン樹脂(PP2)に非晶質アルミノケイ酸塩を混合した。
詳細な条件および各物性の測定・評価結果を表1に示す。
実施例6は、表1に示すように原料、配合量等を変更し、実施例1と同様にして第一層と第二層とを積層した2層のフィルムを作製した後、第一層側表面にコロナ処理を行い、真空蒸着法によるアルミニウムの無機蒸着層(第三層)を10nm設けることで、PTP用蓋材を作製した。実施例1と同様にしてPP底材と蓋材(TPO層側)とを接着し、PTP包装体を得た。
詳細な条件および各物性の測定・評価結果を表1に示す。
比較例4は、表1に示すように原料、配合量等を変更し、実施例1と同様にして第一層と第二層とを積層した2層のフィルムを作製した後、特許文献1を参考に、加速電圧250kV、照射線量60kGyの電子線を照射することでPTP用蓋材を作製した。実施例1と同様にしてPP/PE底材(PE層側)と蓋材(PE層側)とを接着し、PTP包装体を得た。
詳細な条件および各物性の測定・評価結果を表1に示す。
特許文献4を参考に、共押出ダイレクトインフレーション法を用いて、エチレン-酢酸ビニル共重合体ケン化物(EVOH)層(第一層)、酸変性ポリオレフィン組成物層(第二層)、およびポリスチレン樹脂(PS)層(第三層)を積層した3層の積層フィルムを作製した。この際、各層の厚み比がEVOH層:酸変性ポリオレフィン組成物層:PS層=20:10:70となるように調整し、総厚みを40μmとした。
続いて、得られた積層フィルムのPS層面に対し、エチレン酢酸ビニル(EVA)系エマルジョン型ヒートシール剤を乾燥膜厚が9μmになるように塗布し、PTP用蓋材を作製した。その後、実施例1と同様にしてPVC底材と蓋材(ヒートシール剤側)とを接着し、PTP包装体を得た。
詳細な条件および各物性の測定・評価結果を表1に示す。
特許文献5を参考に、2種のポリプロピレン(PP3およびPP4)を共押出により積層させ、ダイから押し出したフィルムを冷水にて冷却することで、2層の未延伸積層フィルムを作製した。次に、未延伸積層フィルムを140℃に加熱し、MDに4倍延伸した後、押出ラミネートによりプロピレン-α-オレフィンコポリマー(TPO)をPP3層上に積層させ、3層の積層フィルムを作製した。次いで、テンター式延伸機にて140℃でTDに5倍延伸することで、PTP用蓋材を作製した。この際、各層の厚み比がPP4:PP3:TPO=20:10:70となるように調整し、総厚みを40μmとした。実施例1と同様にしてPP底材と蓋材(TPO層側)とを接着し、PTP包装体を得た。
詳細な条件および各物性の測定・評価結果を表1に示す。
2 PTP用蓋材
3 底材
4 凹部
5 フランジ部
6 内容物
Claims (7)
- 重量平均分子量が2.0×105~3.5×105であるポリプロピレン系樹脂を含み、示差走査熱量計(DSC)による結晶融解熱量が70J/g以上であることを特徴とする、PTP用蓋材。
- MD配向度が-0.035~0.035である、請求項1に記載のPTP用蓋材。
- 前記PTP用蓋材の突刺試験時の荷重-変位曲線において、破断領域における変位0.1mmあたりの最大荷重低下が3~20Nである、請求項1または2に記載のPTP用蓋材。
- 厚みが10~100μmであり、水蒸気透過度が10g/m2・day以下であり、引張強度がMDおよびTDいずれも20~50MPaであり、かつ引張伸度がMDおよびTDいずれも15%以下である、請求項1~3のいずれか一項に記載のPTP用蓋材。
- 無機物を0.1~3質量%含む、請求項1~4のいずれか一項に記載のPTP用蓋材。
- 前記ポリプロピレン系樹脂を含む層と、ポリエチレン系樹脂、ポリプロピレン系樹脂、またはポリオレフィン系エラストマーを含む少なくとも1つの表層とを含む、請求項1~5のいずれか一項に記載のPTP用蓋材。
- 請求項1~6のいずれか一項に記載のPTP用蓋材と、内容物を収容する凹部を有する底材とを含むことを特徴とする、PTP包装体。
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US18/253,920 US20240002123A1 (en) | 2020-11-24 | 2021-10-18 | Lid material for ptp and ptp body |
CN202180075573.9A CN116457286A (zh) | 2020-11-24 | 2021-10-18 | Ptp用盖材和ptp包装体 |
KR1020237006478A KR20230042733A (ko) | 2020-11-24 | 2021-10-18 | Ptp 용 덮개재 및 ptp 포장체 |
CA3199705A CA3199705A1 (en) | 2020-11-24 | 2021-10-18 | Lid material for ptp and ptp body |
EP21897544.9A EP4253278A4 (en) | 2020-11-24 | 2021-10-18 | COVERING MATERIAL FOR PTP AND PTP PACKAGE |
JP2022565109A JP7416978B2 (ja) | 2020-11-24 | 2021-10-18 | Ptp用蓋材およびptp包装体 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2020-194643 | 2020-11-24 | ||
JP2020194643 | 2020-11-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2022113566A1 true WO2022113566A1 (ja) | 2022-06-02 |
Family
ID=81754288
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2021/038438 WO2022113566A1 (ja) | 2020-11-24 | 2021-10-18 | Ptp用蓋材およびptp包装体 |
Country Status (7)
Country | Link |
---|---|
US (1) | US20240002123A1 (ja) |
EP (1) | EP4253278A4 (ja) |
JP (1) | JP7416978B2 (ja) |
KR (1) | KR20230042733A (ja) |
CN (1) | CN116457286A (ja) |
CA (1) | CA3199705A1 (ja) |
WO (1) | WO2022113566A1 (ja) |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH09240727A (ja) * | 1996-03-08 | 1997-09-16 | Sumitomo Bakelite Co Ltd | Ptp用蓋材シート |
JPH11105217A (ja) * | 1997-10-06 | 1999-04-20 | Tohcello Co Ltd | プレススルーパックカバー用積層フィルム |
JP2012001588A (ja) * | 2010-06-15 | 2012-01-05 | Mitsubishi Plastics Inc | プロピレン系シート |
WO2018235835A1 (ja) * | 2017-06-20 | 2018-12-27 | 旭化成株式会社 | プレススルーパック包装体用蓋材 |
JP2021030501A (ja) * | 2019-08-20 | 2021-03-01 | 三菱ケミカル株式会社 | ストレッチ包装用フィルム |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH07256842A (ja) | 1994-03-23 | 1995-10-09 | Dainippon Printing Co Ltd | プレススルー機能を有する蓋材 |
JP3173767B2 (ja) | 1996-09-30 | 2001-06-04 | 住友ベークライト株式会社 | Ptp用蓋材シート |
JP2000007026A (ja) | 1998-06-19 | 2000-01-11 | Gunze Ltd | ブリスタ−パック包装体の蓋材用シート |
JP2000025173A (ja) | 1998-07-08 | 2000-01-25 | Toray Ind Inc | 積層ポリプロピレン系フイルム |
JP2013234002A (ja) | 2013-07-04 | 2013-11-21 | Asahi Kasei Chemicals Corp | プレススルーパック用蓋材フィルム及び包装体 |
-
2021
- 2021-10-18 JP JP2022565109A patent/JP7416978B2/ja active Active
- 2021-10-18 CA CA3199705A patent/CA3199705A1/en active Pending
- 2021-10-18 CN CN202180075573.9A patent/CN116457286A/zh active Pending
- 2021-10-18 WO PCT/JP2021/038438 patent/WO2022113566A1/ja active Application Filing
- 2021-10-18 EP EP21897544.9A patent/EP4253278A4/en active Pending
- 2021-10-18 US US18/253,920 patent/US20240002123A1/en active Pending
- 2021-10-18 KR KR1020237006478A patent/KR20230042733A/ko unknown
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH09240727A (ja) * | 1996-03-08 | 1997-09-16 | Sumitomo Bakelite Co Ltd | Ptp用蓋材シート |
JPH11105217A (ja) * | 1997-10-06 | 1999-04-20 | Tohcello Co Ltd | プレススルーパックカバー用積層フィルム |
JP2012001588A (ja) * | 2010-06-15 | 2012-01-05 | Mitsubishi Plastics Inc | プロピレン系シート |
WO2018235835A1 (ja) * | 2017-06-20 | 2018-12-27 | 旭化成株式会社 | プレススルーパック包装体用蓋材 |
JP2021030501A (ja) * | 2019-08-20 | 2021-03-01 | 三菱ケミカル株式会社 | ストレッチ包装用フィルム |
Non-Patent Citations (1)
Title |
---|
See also references of EP4253278A4 * |
Also Published As
Publication number | Publication date |
---|---|
JPWO2022113566A1 (ja) | 2022-06-02 |
EP4253278A1 (en) | 2023-10-04 |
CA3199705A1 (en) | 2022-06-02 |
CN116457286A (zh) | 2023-07-18 |
KR20230042733A (ko) | 2023-03-29 |
JP7416978B2 (ja) | 2024-01-17 |
US20240002123A1 (en) | 2024-01-04 |
EP4253278A4 (en) | 2024-05-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP4894340B2 (ja) | ヒートシール性積層ポリプロピレン系樹脂フイルム及び包装体 | |
US20060210801A1 (en) | Resin composition having an easy-to-open property and use thereof | |
JP4887343B2 (ja) | 多層フィルム及び該多層フィルムを用いた包装容器 | |
JP5968543B2 (ja) | 易開封性積層フィルム及びその用途 | |
WO2005092612A1 (ja) | ヒートシール性ポリプロピレン系樹脂積層フィルム及び包装体 | |
JP2021030533A (ja) | 樹脂フィルム及びラミネートチューブ容器 | |
WO2022113566A1 (ja) | Ptp用蓋材およびptp包装体 | |
WO2022113565A1 (ja) | Ptp用蓋材およびptp包装体 | |
JP7444761B2 (ja) | Ptp用蓋材およびptp包装体 | |
JP2012201392A (ja) | 包装用フィルム、積層包装用フィルム、前記フィルムの製造方法、および前記フィルムを用いた包装方法 | |
JP5023924B2 (ja) | 電子レンジ調理用袋 | |
JP4126975B2 (ja) | ヒートシール性フィルム、及びそれを用いた積層体 | |
JP7059648B2 (ja) | 多層シート、トレイ及び包装体 | |
JP2023172392A (ja) | Ptp用蓋材およびその製造方法 | |
JP2023172393A (ja) | Ptp蓋材用フィルム、その製造方法およびptp包装体 | |
JP2018090658A (ja) | シーラント用接着剤及び易剥離性フィルム | |
JP6822198B2 (ja) | シーラント用接着剤及び易剥離性フィルム | |
JP2023172391A (ja) | Ptp用蓋材およびその製造方法 | |
JP2023113473A (ja) | Ptp用シート及び成形体 | |
JP2012001588A (ja) | プロピレン系シート | |
JP2007021814A (ja) | 容器のフタ材用積層ポリプロピレン系樹脂フイルム | |
JP2024036851A (ja) | シーラント用樹脂組成物、積層体、蓋材および包装体 | |
JP2024036850A (ja) | シーラント用樹脂組成物、積層体、蓋材および包装体 | |
JP6572563B2 (ja) | 樹脂組成物及び易剥離性フィルム | |
JP2022029593A (ja) | ポリオレフィン系シート、プレススルーパッケージ包装用底材およびプレススルーパッケージ包装材 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 21897544 Country of ref document: EP Kind code of ref document: A1 |
|
ENP | Entry into the national phase |
Ref document number: 2022565109 Country of ref document: JP Kind code of ref document: A |
|
ENP | Entry into the national phase |
Ref document number: 20237006478 Country of ref document: KR Kind code of ref document: A |
|
WWE | Wipo information: entry into national phase |
Ref document number: 202180075573.9 Country of ref document: CN |
|
ENP | Entry into the national phase |
Ref document number: 3199705 Country of ref document: CA |
|
WWE | Wipo information: entry into national phase |
Ref document number: 18253920 Country of ref document: US |
|
REG | Reference to national code |
Ref country code: BR Ref legal event code: B01A Ref document number: 112023009767 Country of ref document: BR |
|
ENP | Entry into the national phase |
Ref document number: 112023009767 Country of ref document: BR Kind code of ref document: A2 Effective date: 20230519 |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
ENP | Entry into the national phase |
Ref document number: 2021897544 Country of ref document: EP Effective date: 20230626 |