EP2777934A1 - Barrier paper packaging material - Google Patents
Barrier paper packaging material Download PDFInfo
- Publication number
- EP2777934A1 EP2777934A1 EP12847115.8A EP12847115A EP2777934A1 EP 2777934 A1 EP2777934 A1 EP 2777934A1 EP 12847115 A EP12847115 A EP 12847115A EP 2777934 A1 EP2777934 A1 EP 2777934A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- barrier layer
- water vapor
- packaging material
- vapor barrier
- coating
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 230000004888 barrier function Effects 0.000 title claims abstract description 331
- 239000005022 packaging material Substances 0.000 title claims abstract description 84
- 239000010410 layer Substances 0.000 claims abstract description 203
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 182
- 239000000463 material Substances 0.000 claims abstract description 67
- 229920005989 resin Polymers 0.000 claims abstract description 55
- 239000011347 resin Substances 0.000 claims abstract description 55
- 239000011247 coating layer Substances 0.000 claims abstract description 24
- 239000011230 binding agent Substances 0.000 claims abstract description 20
- 229920000642 polymer Polymers 0.000 claims abstract description 14
- 229920003169 water-soluble polymer Polymers 0.000 claims abstract description 14
- 238000000576 coating method Methods 0.000 claims description 144
- 239000011248 coating agent Substances 0.000 claims description 142
- 239000000123 paper Substances 0.000 claims description 128
- 239000000049 pigment Substances 0.000 claims description 90
- 239000002245 particle Substances 0.000 claims description 69
- 239000005995 Aluminium silicate Substances 0.000 claims description 49
- 235000012211 aluminium silicate Nutrition 0.000 claims description 49
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims description 49
- 239000003431 cross linking reagent Substances 0.000 claims description 35
- 239000002174 Styrene-butadiene Substances 0.000 claims description 18
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical group C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 claims description 18
- 239000011115 styrene butadiene Substances 0.000 claims description 18
- 229920003048 styrene butadiene rubber Polymers 0.000 claims description 18
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 16
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 9
- 229920003002 synthetic resin Polymers 0.000 claims description 8
- 239000000057 synthetic resin Substances 0.000 claims description 8
- 239000007789 gas Substances 0.000 description 96
- 239000007788 liquid Substances 0.000 description 77
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 25
- 239000001301 oxygen Substances 0.000 description 25
- 229910052760 oxygen Inorganic materials 0.000 description 25
- 239000007787 solid Substances 0.000 description 18
- 239000004816 latex Substances 0.000 description 15
- 229920000126 latex Polymers 0.000 description 15
- 230000035699 permeability Effects 0.000 description 15
- 239000003795 chemical substances by application Substances 0.000 description 14
- 238000002156 mixing Methods 0.000 description 14
- 238000000034 method Methods 0.000 description 13
- 229910052751 metal Inorganic materials 0.000 description 12
- 239000002184 metal Substances 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 11
- -1 silicate ion Chemical class 0.000 description 11
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 10
- 239000001023 inorganic pigment Substances 0.000 description 10
- 239000000126 substance Substances 0.000 description 10
- 230000000694 effects Effects 0.000 description 9
- 239000010445 mica Substances 0.000 description 9
- 229910052618 mica group Inorganic materials 0.000 description 9
- 239000002002 slurry Substances 0.000 description 9
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 8
- 229910052901 montmorillonite Inorganic materials 0.000 description 8
- GNHOJBNSNUXZQA-UHFFFAOYSA-J potassium aluminium sulfate dodecahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.O.O.[Al+3].[K+].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O GNHOJBNSNUXZQA-UHFFFAOYSA-J 0.000 description 8
- 238000002360 preparation method Methods 0.000 description 8
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 7
- 235000011126 aluminium potassium sulphate Nutrition 0.000 description 7
- 230000015556 catabolic process Effects 0.000 description 7
- 239000004927 clay Substances 0.000 description 7
- 238000006731 degradation reaction Methods 0.000 description 7
- 229910052500 inorganic mineral Inorganic materials 0.000 description 7
- 239000011707 mineral Substances 0.000 description 7
- 229940050271 potassium alum Drugs 0.000 description 7
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 6
- 229920001131 Pulp (paper) Polymers 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 6
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 6
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 6
- 239000002270 dispersing agent Substances 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 6
- 238000001125 extrusion Methods 0.000 description 6
- 239000002655 kraft paper Substances 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 238000004132 cross linking Methods 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 229920002401 polyacrylamide Polymers 0.000 description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 238000003475 lamination Methods 0.000 description 4
- 239000012860 organic pigment Substances 0.000 description 4
- 239000002798 polar solvent Substances 0.000 description 4
- 229940088417 precipitated calcium carbonate Drugs 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 239000000454 talc Substances 0.000 description 4
- 229910052623 talc Inorganic materials 0.000 description 4
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 3
- 229920006243 acrylic copolymer Polymers 0.000 description 3
- 239000000654 additive Substances 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
- 239000002518 antifoaming agent Substances 0.000 description 3
- 239000011575 calcium Substances 0.000 description 3
- 229910052791 calcium Inorganic materials 0.000 description 3
- 229910000019 calcium carbonate Inorganic materials 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000008119 colloidal silica Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000011258 core-shell material Substances 0.000 description 3
- 239000002612 dispersion medium Substances 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 230000001747 exhibiting effect Effects 0.000 description 3
- 239000010419 fine particle Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 230000001105 regulatory effect Effects 0.000 description 3
- 239000005871 repellent Substances 0.000 description 3
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 3
- 235000012239 silicon dioxide Nutrition 0.000 description 3
- 238000004513 sizing Methods 0.000 description 3
- 238000005728 strengthening Methods 0.000 description 3
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 239000002562 thickening agent Substances 0.000 description 3
- 239000004408 titanium dioxide Substances 0.000 description 3
- 238000004078 waterproofing Methods 0.000 description 3
- 239000011787 zinc oxide Substances 0.000 description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 229910052788 barium Inorganic materials 0.000 description 2
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 2
- 229910052810 boron oxide Inorganic materials 0.000 description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 description 2
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 2
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000007850 fluorescent dye Substances 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 150000001261 hydroxy acids Chemical class 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 238000010030 laminating Methods 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 229940085991 phosphate ion Drugs 0.000 description 2
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000000565 sealant Substances 0.000 description 2
- 150000004760 silicates Chemical class 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 239000010936 titanium Substances 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- 229910052726 zirconium Inorganic materials 0.000 description 2
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 235000017166 Bambusa arundinacea Nutrition 0.000 description 1
- 235000017491 Bambusa tulda Nutrition 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 229920000219 Ethylene vinyl alcohol Polymers 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 240000000797 Hibiscus cannabinus Species 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 229920000881 Modified starch Polymers 0.000 description 1
- 239000004368 Modified starch Substances 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 244000082204 Phyllostachys viridis Species 0.000 description 1
- 235000015334 Phyllostachys viridis Nutrition 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- BCKXLBQYZLBQEK-KVVVOXFISA-M Sodium oleate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC([O-])=O BCKXLBQYZLBQEK-KVVVOXFISA-M 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 229920002522 Wood fibre Polymers 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- RSWGJHLUYNHPMX-ONCXSQPRSA-N abietic acid Chemical compound C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C(O)=O RSWGJHLUYNHPMX-ONCXSQPRSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
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- 125000000217 alkyl group Chemical group 0.000 description 1
- 229940037003 alum Drugs 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
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
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- 239000011425 bamboo Substances 0.000 description 1
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- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
- FXBZWPXBAZFWIY-UHFFFAOYSA-N butyl prop-2-enoate;ethenyl acetate Chemical compound CC(=O)OC=C.CCCCOC(=O)C=C FXBZWPXBAZFWIY-UHFFFAOYSA-N 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
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- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
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- 150000002148 esters Chemical class 0.000 description 1
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- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 239000006081 fluorescent whitening agent Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000005003 food packaging material Substances 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910052809 inorganic oxide Inorganic materials 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- HTEAGOMAXMOFFS-UHFFFAOYSA-N methyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C(C)=C HTEAGOMAXMOFFS-UHFFFAOYSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000001254 oxidized starch Substances 0.000 description 1
- 235000013808 oxidized starch Nutrition 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000010893 paper waste Substances 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920005596 polymer binder Polymers 0.000 description 1
- 239000002491 polymer binding agent Substances 0.000 description 1
- 239000002952 polymeric resin Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000013055 pulp slurry Substances 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 239000004320 sodium erythorbate Substances 0.000 description 1
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 1
- 235000019982 sodium hexametaphosphate Nutrition 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 230000002123 temporal effect Effects 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 239000002025 wood fiber Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H27/00—Special paper not otherwise provided for, e.g. made by multi-step processes
- D21H27/10—Packing paper
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H19/00—Coated paper; Coating material
- D21H19/36—Coatings with pigments
- D21H19/38—Coatings with pigments characterised by the pigments
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H19/00—Coated paper; Coating material
- D21H19/36—Coatings with pigments
- D21H19/44—Coatings with pigments characterised by the other ingredients, e.g. the binder or dispersing agent
- D21H19/56—Macromolecular organic compounds or oligomers thereof obtained by reactions only involving carbon-to-carbon unsaturated bonds
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H19/00—Coated paper; Coating material
- D21H19/36—Coatings with pigments
- D21H19/44—Coatings with pigments characterised by the other ingredients, e.g. the binder or dispersing agent
- D21H19/56—Macromolecular organic compounds or oligomers thereof obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H19/58—Polymers or oligomers of diolefins, aromatic vinyl monomers or unsaturated acids or derivatives thereof
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H19/00—Coated paper; Coating material
- D21H19/36—Coatings with pigments
- D21H19/44—Coatings with pigments characterised by the other ingredients, e.g. the binder or dispersing agent
- D21H19/56—Macromolecular organic compounds or oligomers thereof obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H19/60—Polyalkenylalcohols; Polyalkenylethers; Polyalkenylesters
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H19/00—Coated paper; Coating material
- D21H19/80—Paper comprising more than one coating
- D21H19/82—Paper comprising more than one coating superposed
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H19/00—Coated paper; Coating material
- D21H19/80—Paper comprising more than one coating
- D21H19/82—Paper comprising more than one coating superposed
- D21H19/822—Paper comprising more than one coating superposed two superposed coatings, both being pigmented
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
- D21H21/50—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by form
- D21H21/52—Additives of definite length or shape
Definitions
- the present invention relates to a paper barrier material used for a food packaging material, a food container, a food cup or the like.
- gas barrier property in particular, an oxygen barrier property
- Paper packaging materials have hitherto been provided to which a gas barrier property is imparted by laminating a metal foil or a film on a paper base material.
- the material forming the barrier layer include: a metal foil or a metal vapor deposited film made of a metal such as aluminum; a resin film made of polyvinyl alcohol, ethylene-vinyl alcohol copolymer, polyvinylidene chloride or polyacrylonitrile; a film coated with such a resin; and a ceramic vapor-deposited film which is further coated with a vapor-deposited inorganic oxide such as silicon oxide or aluminum oxide.
- Patent Literature 1 paper gas barrier materials having a gas barrier layer made of a water soluble polymer and an inorganic layered compound have been disclosed in Patent Literature 1 and Patent Literature 2.
- Patent Literature 2 A paper gas barrier material in which a barrier layer made of a specific vinyl alcohol-based polymer is provided on a coating layer is disclosed in Patent Literature 2.
- a waterproofness in particular, a water vapor barrier property
- a paper packaging material for the purpose of protecting various products to be packaged from the degradation due to water vapor.
- a paper packaging material has been proposed in which a water vapor barrier property is imparted by extrusion lamination of or pasting of a resin film excellent in water vapor barrier property onto a paper base material, or alternatively, by extrusion lamination of or pasting of, for example, a film coated with such a resin excellent in water vapor barrier property on a paper base material.
- a packaging paper having a moistureproof layer composed of a synthetic resin latex, a wax and inorganic fine particles is disclosed in Patent Literature 3.
- a packaging material in which both of a gas barrier property and a water vapor barrier are imparted to a paper packaging material
- a packaging material in which a resin having a gas barrier property and a resin having a water vapor barrier property are laminated on a paper base material.
- a packaging material in which by extrusion lamination of a resin having a gas barrier property and a resin having a water vapor barrier property on a paper base material (base paper), both barrier layers are formed on the paper base material has a problem that the packaging material cannot cope with the required quality because the types and the like of the resins capable of being extrusion laminated are limited.
- a packaging material in which multilayers are laminated on a paper base material in order to establish the compatibility between the gas barrier property and the water vapor barrier property finds difficulty in recycling of the paper and the laminated layers.
- the multilayer laminated packaging material also offers a problem such that the carbon dioxide emission amount in the production thereof is large.
- specific adhesive resins are sometimes required to be used between the respective laminated layers, to offer another problem that the production of the multilayer laminated packaging material is cumbersome.
- a packaging material in which a paper base material is coated with a resin having a gas barrier property and a resin having a water vapor barrier property the types and the like of the usable resins are scarcely limited, and various required qualities can be coped with.
- a packaging material to which both of the gas barrier property and the water vapor barrier property are imparted for example, in the case where the moistureproof layer of Patent Literature 3 is disposed on the packaging material having a gas barrier property of Patent Literature 1 or Patent Literature 2, offers a problem that although a satisfactory water vapor barrier property is obtained, no gas barrier property is obtained.
- the gas barrier layer of Patent Literature 1 or Patent Literature 2 is disposed on a moistureproof paper having the moistureproof layer of Patent Literature 3, the surface tension of the moistureproof layer, hence the gas barrier layer is not uniformly formed due to repellency, and hence no sufficient gas barrier property can be obtained.
- the present invention takes as its object the provision of a paper based barrier packaging material simultaneously having both of an excellent gas barrier property and an excellent water vapor barrier property.
- the main constitution of the present invention is as follows.
- the present invention is a paper based barrier packaging material (hereinafter, sometimes referred to as a "packaging material”) including a water vapor barrier layer and a gas barrier layer disposed in this order on a paper base material (hereinafter, sometimes referred to as a "base paper").
- the two types of the barrier layers are each formed by applying an aqueous coating material, and to the coating material, a polymer binder as a main additive, a pigment, a cross-linking agent and the like are added.
- the water vapor barrier layer or the gas barrier layer is formed by coating with a coating material including a polymer as a binder resin and using water as a dispersion medium.
- a coating material including a polymer as a binder resin and using water as a dispersion medium.
- the paper based barrier packaging material of the present invention including the water vapor barrier layer formed on a paper base material and further the gas barrier layer on the water vapor barrier layer simultaneously has both of an excellent water vapor barrier property and an excellent gas barrier property are inferred as follows.
- the paper based barrier packaging material of the present invention has a satisfactory water vapor barrier property and a satisfactory gas barrier property.
- the paper based barrier packaging material of the present invention is usually used in such a way that the side of the gas barrier layer is the side of the content (article to be packaged) and the side of the paper layer is the atmospheric side (outer surface).
- the permeation of the atmospheric moisture into the interior can be prevented, and hence when the article to be packaged is a dry substance, the structure of the present invention is effective.
- a resin extrusion laminated layer or a film laminate layer is additionally formed on the gas barrier layer to be the inner side.
- the paper base material is a sheet includes pulp, a filler, and various additives.
- the pulp include: chemical pulps such as leaf bleached kraft pulp (LBKP), needle bleached kraft pulp (NBKP) and sulfite pulp; mechanical pulps such as stone-ground pulp and thermomechanical pulp; and non-wood fibers obtained from kenaf, bamboo, hemp and the like. These materials can be appropriately mixed to be used.
- the chemical pulps such as leaf bleached kraft pulp (LBKP) and needle bleached kraft pulp (NBKP) are preferable.
- the chemical pulps are suitable, for example, for the reasons that contamination of the base paper hardly occurs, temporal discoloration hardly occurs when used paper containers are collected as waste paper raw materials to be recycled, and chemical pulps have a high degree of whiteness to result in satisfactory surface touch at the time of printing so as to enhance the value in use as packaging materials.
- the usable filler examples include heretofore known fillers such as white carbon, talc, kaolin, clay, heavy calcium carbonate, precipitated calcium carbonate, titanium oxide, zeolite and synthetic resin fillers.
- the following papermaking internal aids can also be used: aluminum sulfate; various anionic, cationic, nonionic, or amphoteric yield improvers; a freeness improver, a paper-strengthening agent and an internal sizing agent.
- a dye, a fluorescent whitening agent, a pH adjuster, an antifoaming agent, a pitch control agent, a slime control agent and the like can also be added.
- the method of the production (paper making) of the paper base material is not particularly limited; paper base materials can be produced by using heretofore known fourdrinier former, on-top hybrid former and gap former machines, and by performing paper making with acidic paper making, neutral paper making, alkaline paper making methods.
- the paper base material is preferably a material generally used for coated papers, having a basis weight of about 25 to 400 g/m 2 .
- the surface of the paper base material can be treated with various chemicals.
- Examples of the chemicals to be used may include: oxidized starch, hydroxyethyl etherified starch, oxygen-modified starch, polyacrylamide, polyvinyl alcohol, a surface sizing agent, a waterproofing agent, a water retention agent, a thickener and a lubricant; these can be used each alone or in combinations of two or more thereof.
- the method of the surface treatment of the paper base material is not particularly limited; however, heretofore known coating apparatuses such as a rod metering size press, a pond type size press, a gate roll coater, a spray coater, a blade coater and a curtain coater can be used.
- the polymer to be used as the main component of the coating layer forming the water vapor barrier layer or the gas barrier layer is suitably a resin for which water can be used as a dispersion medium.
- the dosage form include a polymer aqueous solution and a form of a polymer emulsion.
- the polymer corresponds to the binder of the coating material for forming a coating layer.
- the following resins can be used each alone or as mixtures of two or more thereof: copolymers such as styrene-butadiene-based, styrene-acrylic, ethylene-vinyl acetate-based, butadiene-methyl methacrylate-based, vinyl acetate-butyl acrylate-based copolymers; maleic anhydride copolymer; and acrylic acid-methyl methacrylate-based copolymer.
- styrene-butadiene-based resin is preferable from the viewpoint of the water vapor barrier property.
- styrene-butadiene-based synthetic resin is a resin synthesized with emulsion polymerization by using styrene and butadiene as the main constituent monomers in combination with various comonomers aiming at modification.
- the comonomer include: methyl methacrylate, acrylonitrile, acrylamide and hydroxyethyl acrylate; and unsaturated carboxylic acids such as itaconic acid, maleic acid and acrylic acid.
- the resins are used as emulsion-type coating materials prepared by emulsification with water as a dispersant.
- the emulsifier include anionic surfactants such as sodium oleate, rosin acid soap, sodium alkyl allyl sulfonate and sodium dialkyl sulfosuccinate. These can be used each alone or in combinations with nonionic surfactants. Moreover, if necessary, amphoteric or cationic surfactants may also be used.
- the coating material to form the water vapor barrier layer preferably does not include water-repellent components such as a hydrocarbon, a silicone-based resin, a fluorine-based resin, a fatty acid and an ester between a fatty acid and an alcohol.
- water-repellent components such as a hydrocarbon, a silicone-based resin, a fluorine-based resin, a fatty acid and an ester between a fatty acid and an alcohol.
- conventional packaging materials having a water vapor barrier property are generally provided with water-repellent component-containing resins.
- the water-repellent component degrades the affinity between the water vapor barrier layer and the gas barrier layer, and accordingly, the moisture or gas permeating from one of these layers unpreferably promotes interfacial peeling.
- the inclusion of a pigment in the water vapor barrier layer improves the water vapor barrier property, and also improves the adhesion between the water vapor barrier layer and the gas barrier layer.
- the pigment examples include an inorganic pigment and an organic pigment.
- the inorganic pigment examples include: kaolin, clay, engineered kaolin, delaminated clay, heavy calcium carbonate, precipitated calcium carbonate, talc, titanium dioxide, barium sulfate, calcium sulfate, zinc oxide, silicic acid, silicates, colloidal silica and satin white.
- the organic pigment examples include a dense-type pigment, a hollow-type pigment, or a core-shell type pigment. These pigments can be used each alone or as mixtures of two or more thereof.
- the pigments flat in shape and large in size are suitable.
- the water vapor barrier property is improved by using a pigment large in particle size and a pigment small in particle size in combination.
- inorganic pigments such as flat-shaped kaolin improve the water vapor barrier property.
- kaolin having an average particle size of 5 ⁇ m or more and an aspect ratio of 10 or more is more preferable.
- a flat pigment is distributed parallel to the coating layer, the water vapor permeating into the water vapor barrier layer is blocked by the flat pigment with respect to the movement in the thickness direction and is made to move in a detour so as to elongate the path of the passage of the water vapor through the water vapor barrier layer, and hence the barrier property is improved.
- the aspect ratio of the added pigment is small, the number of times of detour of the water vapor in the coating layer is decreased, accordingly the distance of the movement of the water vapor is reduced, and consequently the pigment small in aspect ratio is inferior to the flat pigment having a large particle size.
- a flat pigment can be expected to have the same effect as described above on the gas barrier layer.
- mica and montmorillonite can also be used.
- the dispersion of mica or montmorillonite is lower in concentration than the dispersion of kaolin, accordingly the coating liquid for the water vapor barrier layer using mica or montmorillonite is low in concentration so as for the pigment to find difficulty in orientation in the formed water vapor barrier layer, and hence kaolin is more suitable than mica or montmorillonite.
- the water vapor barrier property can be further improved.
- the pigment having a small particle size is not required to be flat.
- a pigment having an average particle size of 5 ⁇ m or less in the water vapor barrier layer including kaolin having an average particle size of 5 ⁇ m or more and an aspect ratio of 10 or more it is preferable to further include a pigment having an average particle size of 5 ⁇ m or less in the water vapor barrier layer including kaolin having an average particle size of 5 ⁇ m or more and an aspect ratio of 10 or more.
- a pigment having an average particle size of 5 ⁇ m or less is interposed between the kaolin particles present in a multilayered manner, having an average particle size of 5 ⁇ m or more and an aspect ratio of 10 or more, and consequently, the water vapor being forced to move along the flat plane of kaolin is blocked in its movement by the smaller pigment particles.
- the pigments different in flatness and average particle size are included in the water vapor barrier layer, a state occurs in which in the water vapor barrier layer, the pigment of smaller particle size is filled in the voids formed between the adjacent flat pigment particles large in particle size, accordingly the water vapor passes all the way around the pigments, and hence the water vapor barrier layer including the pigments different in average particle size exhibits a higher water vapor barrier property as compared to the water vapor barrier layer including no pigment smaller in particle size.
- the mixing ratio between kaolin having an average particle size of 5 ⁇ m or more and an aspect ratio of 10 or more and the pigment having an average particle size of 5 ⁇ m or less is preferably 50/50 to 99/1 in terms of dry weight.
- the ratio of kaolin having an average particle size of 5 ⁇ m or more and an aspect ratio of 10 or more is smaller than the foregoing range, the detour distance of the water vapor in the coating layer is short, and hence no sufficient water vapor barrier property can be obtained.
- the ratio of kaolin having an average particle size of 5 ⁇ m or more and an aspect ratio of 10 or more is larger than the foregoing range, the voids formed by the large particle size pigment in the coating layer cannot be sufficiently filled by the pigment having an average particle size of 5 ⁇ m or less, and hence no improvement of the water vapor barrier property is found.
- the following pigments can be used each alone or as mixtures of two or more thereof: inorganic pigments such as kaolin, clay, engineered kaolin, delaminated clay, heavy calcium carbonate, precipitated calcium carbonate, talc, titanium dioxide, barium sulfate, calcium sulfate, zinc oxide, silicic acid, silicates, colloidal silica and satin white; and organic pigments such as a dense-type pigment, a hollow-type pigment, or a core-shell type pigment. Among these pigments, heavy calcium carbonate is preferable.
- the mixing amounts of the resin and the pigment are such that a resin is used in an amount of preferably 5 to 200 parts by weight and more preferably 20 to 150 parts by weight (dry weight) in relation to 100 parts by weight (dry weight) of the pigment.
- various usually used aids such as a dispersant, a thickener, a water retention agent, an antifoaming agent, a waterproofing agent, a dye and a fluorescent dye.
- a cross-linking agent typified by a multivalent metal salt
- the cross-linking agent causes a cross-linking reaction with the binder included in the water vapor barrier layer, and accordingly the number of the bonds (the number of the cross-linked points) in the water vapor barrier layer is increased.
- the water vapor barrier layer becomes dense in structure, and consequently exhibits a satisfactory water vapor barrier property.
- the type of the cross-linking agent is not particularly limited; the cross-linking agent appropriately according to the type of the binder included in the water vapor barrier layer from the following can be used: multivalent metal salts (the compounds produced by bonding the multivalent metals such as copper, zinc, silver, iron, potassium, sodium, zirconium, aluminum, calcium, barium, magnesium and titanium with the ionic substances such as carbonate ion, sulfate ion, nitrate ion, phosphate ion, silicate ion, nitrogen oxide and boron oxide); and amine compounds, amide compounds, aldehyde compounds, and hydroxy acids.
- multivalent metal salts the compounds produced by bonding the multivalent metals such as copper, zinc, silver, iron, potassium, sodium, zirconium, aluminum, calcium, barium, magnesium and titanium with the ionic substances such as carbonate ion, sulfate ion, nitrate ion, phosphate ion, silicate ion,
- the cross-linking agent can be mixed without being particularly limited with respect to the mixing amount thereof.
- a multivalent metal salt when a styrene-based water vapor barriering resin exhibiting excellent effects in the water vapor barrier property, such as a styrene-butadiene-based resin or a styrene-acrylic-based resin is used; in particular, potassium alum is more preferable.
- the addition amount of the cross-linking agent is 1 to 10 parts by weight and more preferably 3 to 5 parts by weight in relation to 100 parts by weight of the binder resin used in the water vapor barrier layer.
- the addition amount of the cross-linking agent is less than 1 part by weight, no sufficient effect is obtained, and when the addition amount of the cross-linking agent is larger than 10 parts by weight, the viscosity of the coating liquid is remarkably increased to make the coating operation difficult.
- a cross-linking agent when added to the coating liquid to form the water vapor barrier layer, it is preferable to add the cross-linking agent to the coating liquid after the cross-linking agent is dissolved in a polar solvent such as ammonium hydroxide solution.
- a polar solvent such as ammonium hydroxide solution.
- the contact angle with water of the surface of the water vapor barrier layer disposed on the paper base material is preferably less than 90°, more preferably less than 85° and furthermore preferably less than 80°.
- the contact angle with water is 90° or more, it is difficult to dispose a uniform gas barrier layer on the water vapor barrier layer, and it is difficult to exhibit a high gas barrier property.
- the contact angle with water is less than 90°, it is possible to suppress the repulsion between the water vapor barrier layer and the gas barrier layer so as to suppress the peeling between these two layers.
- the contact angle serves as a measure with which the affinity between the water vapor barrier layer and the gas barrier layer is inferred.
- the method for regulating the contact angle with water of the surface of the water vapor barrier layer is not particularly limited; however, examples of such a method include a method using a resin having a low contact angle with water for the water vapor barrier layer, and a method in which a pigment or the like is added to the resin for the water vapor barrier layer.
- the water soluble polymer used as the binder resin of the coating material to form the gas barrier layer can be exemplified by completely saponified polyvinyl alcohol, partially saponified polyvinyl alcohol, ethylene copolymerized polyvinyl alcohol, polyvinylpyrrolidone, starch, methyl cellulose, carboxymethyl cellulose and sodium alginate.
- polyvinyl alcohol and carboxymethyl cellulose are preferable, and polyvinyl alcohol is furthermore preferable.
- examples of the pigments used in the gas barrier layer include: inorganic pigments such as kaolin, clay, engineered kaolin, delaminated clay, heavy calcium carbonate, precipitated calcium carbonate, talc, titanium dioxide, barium sulfate, calcium sulfate, zinc oxide, silicic acid, silicate, colloidal silica, satin white and mica; and organic pigments such as a dense-type pigment, a hollow-type pigment and a core-shell type pigment. These can be used each alone or as mixtures of two or more thereof. Among these, from the viewpoint of the gas barrier property, it is preferable to use an inorganic pigment.
- inorganic pigments such as kaolin, clay, engineered kaolin, delaminated clay, heavy calcium carbonate, precipitated calcium carbonate, talc, titanium dioxide, barium sulfate, calcium sulfate, zinc oxide, silicic acid, silicate, colloidal silica, satin white and mica
- organic pigments such as a dense-
- an inorganic pigment in particular, kaolin
- an inorganic pigment in particular, kaolin
- an inorganic pigment in particular, kaolin
- a gas such as oxygen passes around the pigment. Consequently, as compared to the gas barrier layer formed of a water soluble polymer including no pigment, the gas barrier layer formed of a water soluble polymer including a pigment has a satisfactory water vapor barrier property and an excellent gas barrier property in a high-humidity atmosphere.
- the mixing ratio (in terms of dry weights) between the pigment and the water soluble polymer included in the gas barrier layer is preferably such that the ratio pigment /water soluble polymer is 1/100 to 1000/100. When the proportion of the pigment falls outside the foregoing range, no sufficient gas barrier property is exhibited.
- a cross-linking agent typified by a multivalent metal salt or the like to the gas barrier layer.
- the cross-linking agent bonds the hydroxyl groups in the water soluble polymer to each other through cross-linked structure, hence the amount of the hydroxyl groups having the loosened bonds (or broken bonds) when the humidity becomes high is decreased to improve the waterproofness of the whole layer, and thus the degradation of the oxygen barrier property under a high humidity can be suppressed.
- the type of the cross-linking agent is not particularly limited; the cross-linking agent appropriately according to the type of the binder included in the water vapor barrier layer from the following can be used: multivalent metal salts (the compounds produced by bonding the multivalent metals such as copper, zinc, silver, iron, potassium, sodium, zirconium, aluminum, calcium, barium, magnesium and titanium with the ionic substances such as carbonate ion, sulfate ion, nitrate ion, phosphate ion, silicate ion, nitrogen oxide and boron oxide); and amine compounds, amide compounds, aldehyde compounds, and hydroxy acids.
- multivalent metal salts the compounds produced by bonding the multivalent metals such as copper, zinc, silver, iron, potassium, sodium, zirconium, aluminum, calcium, barium, magnesium and titanium with the ionic substances such as carbonate ion, sulfate ion, nitrate ion, phosphate ion, silicate ion,
- the cross-linking agent can be mixed without being particularly limited with respect to the mixing amount thereof.
- a multivalent metal salt it is preferable to use a multivalent metal salt and it is more preferable to use potassium alum when a styrene-based water vapor barriering resin exhibiting excellent effects in the water vapor barrier property, such as a styrene-butadiene-based resin or a styrene-acrylic-based resin is used.
- the addition amount of the cross-linking agent is 1 to 10 parts by weight and more preferably 3 to 5 parts by weight in relation to 100 parts by weight of the resin used in the gas barrier layer.
- the addition amount of the cross-linking agent is less than 1 part by weight, no sufficient effect is obtained, and when the addition amount of the cross-linking agent is larger than 10 parts by weight, the viscosity of the coating liquid is remarkably increased to make the coating operation difficult.
- a pigment when a pigment is mixed in a water soluble polymer, it is preferable to add and mix a pigment which is water-dispersed and slurried.
- the gas barrier layer in addition to the water soluble polymer and the pigment, various usually used aids such as a dispersant, a thickener, a water retention agent, an antifoaming agent, a waterproofing agent, a dye and a fluorescent dye.
- various usually used aids such as a dispersant, a thickener, a water retention agent, an antifoaming agent, a waterproofing agent, a dye and a fluorescent dye.
- the coating methods of the water vapor barrier layer and the gas barrier layer are not particularly limited, and heretofore known coating apparatuses can be used.
- a coating apparatus include: a blade coater, a bar coater, a roll coater, an airknife coater, a reverse roll coater, a curtain coater, a spray coater, a size press coater and a gate roll coater.
- a steam heating heater a gas heater, an infrared heater, an electric heater, a hot air heating heater, a microwave, a cylinder dryer and the like.
- the coating amount of the water vapor barrier layer is preferably set at 4 to 30 g/m 2 , more preferably 6 to 25 g/m 2 and furthermore preferably 10 to 20 g/m 2 in terms of dry weight.
- the coating amount is 3 g/m 2 or less, there occur a problem that it is difficult for the coating liquid to perfectly coat the base paper, and hence no sufficient water vapor barrier property is obtained, and a problem that the gas barrier layer penetrates into the paper base material, and hence a uniform gas barrier property is not obtained.
- the coating amount is 30 g/m 2 or more, the drying load at the time of coating operation becomes large, unpreferably from the viewpoint of both of the operational aspect and the cost aspect.
- the coating amount of the gas barrier layer is preferably set at 0.2 to 10 g/m 2 in terms of dry weight.
- the coating amount is less than 0.2 /m 2 , no uniform gas barrier layer can be formed, and hence there is problem that no sufficient gas barrier property is obtained.
- the coating amount is 10 g/m 2 or more, the drying load at the time of coating operation becomes large, unpreferably from the viewpoint of both of the operational aspect and the cost aspect.
- a sealant layer made of a polymer such as polyethylene, polypropylene or polyvinyl acetate on the paper based barrier packaging material including a water vapor barrier layer and a gas barrier layer disposed on a paper base material.
- the method for laminating the sealant layer is not particularly limited; it is possible to use a conventional, heretofore known methods such as a melt-extrusion lamination method, a dry lamination method using a film and a direct melt coating method.
- a raw material pulp was prepared by mixing, with a weight ratio of 80/20, a leaf bleached kraft pulp (LBKP) having a Canadian standard freeness (CSF) of 500 ml and a needle bleached kraft pulp (NBKP) having a CSF of 530 ml.
- LKP leaf bleached kraft pulp
- NKP needle bleached kraft pulp
- polyacrylamide (PAM) having a molecular weight of 2,500,000 as a dry paper-strengthening agent in an amount of 0.1% in relation to the bone-dry weight of the pulp, alkyl ketene dimer (AKD) as sizing agent in an amount of 0.35% in relation to the bone-dry weight of the pulp, a polyamide epichlorohydrin (PAEH)-based resin as a wet paper-strengthening agent in an amount of 0.15% in relation to the bone-dry weight of the pulp, and further polyacrylamide (PAM) having a molecular weight of 10,000,000 as a yield improver in an amount of 0.08% in relation to the bone-dry weight of the pulp were added; and then paper making was performed with a duo former FM-type paper making machine at a rate of 300 m/min to yield a paper having a basis weight of 59 g/m 2 .
- both faces of the obtained paper were coated with polyvinyl alcohol (PVA117, manufactured by Kuraray Co., Ltd.) regulated to a solid content concentration of 2% in an amount of 1.0 g/m 2 by using a rod metering size press, and dried to yield a base paper having a basis weight of 60 g/m 2 .
- the base paper obtained was subjected to a smoothing treatment with a chilled calender at a rate of 300 min/m and at a linear load of 50 kgf/cm, in a single pass.
- Polyvinyl alcohol (PVA117, manufactured by Kuraray Co., Ltd.) was regulated so as to have a solid content concentration of 10% to yield a coating liquid B.
- the base paper obtained was single-side coated with the coating liquid A so as to have a coating amount (dry amount) of 12 g/m 2 at a coating speed of 300 m/min with a blade coater and dried; subsequently, the coated side was single-side coated with the coating liquid B so as to have a coating amount (dry amount) of 2.0 g/m 2 at a coating speed of 300 m/min with a roll coater to yield a paper based barrier packaging material.
- the coating liquid for the oxygen barrier layer to the large particle size engineered kaolin (Barrisurf HX, manufactured by Imerys Minerals Ltd.), sodium polyacrylate was added as a dispersant (in an amount of 0.2 part in relation to the inorganic pigment), and the resulting mixture was dispersed with a Serie mixer to prepare a large particle size kaolin slurry having a solid content concentration of 55%.
- a paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the oxygen barrier layer, potassium alum (aluminum potassium sulfate dodecahydrate, manufactured by Kanto Chemical Co., Inc.) was dissolved so as for the concentration to be 5%, the obtained potassium alum aqueous solution was mixed in an amount of 3 parts in terms of the solid content in relation to polyvinyl alcohol, to prepare a coating liquid having a solid content concentration of 10%, and the thus obtained coating liquid was used.
- potassium alum aluminum potassium sulfate dodecahydrate, manufactured by Kanto Chemical Co., Inc.
- a paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the water vapor barrier layer, a coating liquid in which a heavy calcium carbonate slurry (FMT-75, average particle size: 1.6 ⁇ m, aspect ratio: 1, manufactured by Fimatec Ltd.) was mixed in and stirred with the pigment of the coating liquid A so as for the pigment mixing ratio to be 75:25 was used.
- a coating liquid in which a heavy calcium carbonate slurry FMT-75, average particle size: 1.6 ⁇ m, aspect ratio: 1, manufactured by Fimatec Ltd.
- a paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the water vapor barrier layer, the potassium alum aqueous solution dissolved in Example 3 was mixed in an amount of 3 parts in relation to the pigment in the coating liquid obtained in Example 5 to prepare a coating liquid having a solid content concentration of 50%, and the thus obtained coating liquid was used.
- a paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the oxygen barrier layer, the coating liquid obtained in Example 4 was used, and in the coating liquid for the water vapor barrier layer, the coating liquid obtained in Example 5 was used.
- a paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the oxygen barrier layer, the coating liquid obtained in Example 4 was used, and in the coating liquid for the water vapor barrier layer, the coating liquid obtained in Example 6 was used.
- a paper based barrier packaging material was obtained in the same manner as in Example 2 except that in the coating liquid for the oxygen barrier layer, the large particle size engineered kaolin in the coating liquid obtained in Example 2 was altered to mica (B-82, particle size: 180 ⁇ m, manufactured by Matsuo Sangyo Co., Ltd.).
- a paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the oxygen barrier layer, the large particle size engineered kaolin in the coating liquid obtained in Example 1 was altered to montmorillonite (Nikka Knight A-36, particle size: 400 ⁇ m, manufactured by Toshin Chemicals Co., Ltd.).
- a paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the water vapor barrier layer, the large particle size engineered kaolin in the coating liquid obtained in Example 1 was altered to mica (B-82, particle size: 180 ⁇ m, manufactured by Matsuo Sangyo Co., Ltd.), the pigment dispersion concentration was altered to 20%, and the coating liquid concentration was altered to 30.
- a paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the water vapor barrier layer, the large particle size engineered kaolin in the coating liquid obtained in Example 1 was altered to montmorillonite (Nikka Knight A-36, particle size: 400 ⁇ m, manufactured by Toshin Chemicals Co., Ltd.), the pigment dispersion concentration was altered to 20%, the coating liquid concentration was altered to 30%, and the coating amount was altered to 9 g/m 2 .
- montmorillonite Nakka Knight A-36, particle size: 400 ⁇ m, manufactured by Toshin Chemicals Co., Ltd.
- a paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the water vapor barrier layer, the styrene-butadiene-based latex in Example 1 was altered to an acrylic-styrene-based copolymer emulsion (Saivinol X-511-374E, manufactured by Saiden Chemical Industry Co., Ltd.).
- a paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the water vapor barrier layer, the latex was altered to a styrene-butadiene-based latex (L7360, manufactured by Asahi Kasei Chemicals Corp.).
- a paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the water vapor barrier layer, the pigment used in the coating liquid was altered from the large particle size engineered kaolin (Barrisurf HX, manufactured by Imerys Minerals Ltd.) to the large particle size engineered kaolin (Capim CC, particle size: 8.0 ⁇ m, aspect ratio: 10 to 15, manufactured by Imerys Minerals Ltd.).
- a paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the water vapor barrier layer, the pigment used in the coating liquid was altered from the large particle size engineered kaolin (Barrisurf HX, manufactured by Imerys Minerals Ltd.) to a fine particle kaolin (Hydragloss, average particle size: 0.3 ⁇ m, aspect ratio: 10 to 15, manufactured by KaMin LLC).
- the large particle size engineered kaolin (Barrisurf HX, manufactured by Imerys Minerals Ltd.)
- a fine particle kaolin Heydragloss, average particle size: 0.3 ⁇ m, aspect ratio: 10 to 15, manufactured by KaMin LLC).
- a paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the water vapor barrier layer, the pigment used in the coating liquid was altered from the large particle size engineered kaolin (Barrisurf HX, manufactured by Imerys Minerals Ltd.) to a second grade kaolin (KCS, average particle size: 3.6 ⁇ m, aspect ratio: 10 to 15, manufactured by Imerys Minerals Ltd.).
- a paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the water vapor barrier layer, the latex used in the coating liquid was altered to a styrene-butadiene-based latex (PNT7889, manufactured by ZEON Corp.).
- a paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the water vapor barrier layer, the latex used in the coating liquid was altered to a styrene-butadiene-based latex (L7360, Asahi Kasei Chemicals Corp.).
- a paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the water vapor barrier layer, the latex used in the coating liquid was altered to an acrylic copolymer latex (E316, manufactured by Asahi Kasei Chemicals Corp.).
- a paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the water vapor barrier layer, the latex used in the coating liquid was altered to an acrylic copolymer aqueous emulsion (EK-61, manufactured by Saiden Chemical Industry Co., Ltd.).
- EK-61 acrylic copolymer aqueous emulsion
- a paper based barrier packaging material was obtained in the same manner as in Example 1 except that the coating amount of the coating liquid A was altered from 12 g/m 2 to 6 g/m 2 in terms of dry weight.
- a paper based barrier packaging material was obtained in the same manner as in Example 1 except that the coating amount of the coating liquid A was altered from 12 g/m 2 to 15 g/m 2 in terms of dry weight.
- a paper based barrier packaging material was obtained in the same manner as in Example 1 except that the coating amount of the coating liquid B was altered from 2 g/m 2 to 1 g/m 2 in terms of dry weight.
- a paper based barrier packaging material was obtained in the same manner as in Example 1 except that the coating amount of the coating liquid B was altered from 2 g/m 2 to 4 g/m 2 in terms of dry weight.
- a paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the preparation of the coating liquid for the water vapor barrier layer, the mixing amount of the styrene-butadiene-based latex (PNT7868, manufactured by ZEON Corp.) was altered from 100 parts to 50 parts (solid content) in relation to the pigment.
- the mixing amount of the styrene-butadiene-based latex (PNT7868, manufactured by ZEON Corp.) was altered from 100 parts to 50 parts (solid content) in relation to the pigment.
- a paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the preparation of the coating liquid for the water vapor barrier layer, the mixing amount of the styrene-butadiene-based latex (PNT7868, manufactured by ZEON Corp.) was altered from 100 parts to 150 parts (solid content) in relation to the pigment.
- the mixing amount of the styrene-butadiene-based latex (PNT7868, manufactured by ZEON Corp.) was altered from 100 parts to 150 parts (solid content) in relation to the pigment.
- a paper based barrier packaging material was obtained in the same manner as in Example 1 except that the gas barrier layer and the water vapor barrier layer were disposed in this order on the paper base material.
- a paper based barrier packaging material was obtained in the same manner as in Example 1 except that no water vapor barrier layer was disposed.
- Example 1 A paper based barrier packaging material was obtained in the same manner as in Example 1 except that no gas barrier layer was disposed.
- [Table 1] Coating amount of water vapor barrier layer Contact angle after coating of water vapor barrier layer Water vapor permeability Coating amount of oxygen barrier layer Oxygen permeability (under dry condition) Oxygen permeability (under high humidity) g/m 2 ⁇ g/m 2 ⁇ day g/m 2 g/m 2 ⁇ day g/m 2 ⁇ day Example 1 12.0 75 250 2.0 1.0 200 Example 2 12.0 75 250 2.0 1.0 80 Example 3 12.0 75 250 2.0 1.0 150 Example 4 12.0 75 250 2.0 1.0 50 Example 5 12.0 75 200 2.0 1.0 200 Example 6 12.0 75 150 2.0 1.0 200 Example 7 12.0 75 200 2.0 1.0 50 Example 8 12.0 75 150 2.0 1.0 50 Example 9 12.0 75 250 2.0 1.0 80 Example 10 12.0 75 250 2.0 1.0 80 Example 11 9.0 75 300 2.0 1.0 200 Example 12 9.0 75 300 2.0 1.0 200 Example 13 12.0 90 250 2.0 1.0
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Abstract
Description
- The present invention relates to a paper barrier material used for a food packaging material, a food container, a food cup or the like.
- It is important to impart a gas barrier property (in particular, an oxygen barrier property) to a paper packaging material for the purpose of protecting packaged various products from the degradation due to gas, such as oxidation due to oxygen.
- Paper packaging materials have hitherto been provided to which a gas barrier property is imparted by laminating a metal foil or a film on a paper base material. Examples of the material forming the barrier layer include: a metal foil or a metal vapor deposited film made of a metal such as aluminum; a resin film made of polyvinyl alcohol, ethylene-vinyl alcohol copolymer, polyvinylidene chloride or polyacrylonitrile; a film coated with such a resin; and a ceramic vapor-deposited film which is further coated with a vapor-deposited inorganic oxide such as silicon oxide or aluminum oxide.
- In addition to the foregoing, as paper packaging materials with a gas barrier property imparted thereto, paper gas barrier materials having a gas barrier layer made of a water soluble polymer and an inorganic layered compound have been disclosed in Patent Literature 1 and Patent Literature 2. A paper gas barrier material in which a barrier layer made of a specific vinyl alcohol-based polymer is provided on a coating layer is disclosed in Patent Literature 2.
- It is also important to impart a waterproofness (in particular, a water vapor barrier property) to a paper packaging material for the purpose of protecting various products to be packaged from the degradation due to water vapor.
- A paper packaging material has been proposed in which a water vapor barrier property is imparted by extrusion lamination of or pasting of a resin film excellent in water vapor barrier property onto a paper base material, or alternatively, by extrusion lamination of or pasting of, for example, a film coated with such a resin excellent in water vapor barrier property on a paper base material. A packaging paper having a moistureproof layer composed of a synthetic resin latex, a wax and inorganic fine particles is disclosed in Patent Literature 3.
- Moreover, as a packaging material in which both of a gas barrier property and a water vapor barrier are imparted to a paper packaging material, a packaging material is known in which a resin having a gas barrier property and a resin having a water vapor barrier property are laminated on a paper base material.
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- Patent Literature 1: Japanese Patent Laid-Open No.
2009-184138 - Patent Literature 2: Japanese Patent Laid-Open No.
2003-094574 - Patent Literature 3: Japanese Patent Laid-Open No.
2005-162213 - A packaging material in which by extrusion lamination of a resin having a gas barrier property and a resin having a water vapor barrier property on a paper base material (base paper), both barrier layers are formed on the paper base material has a problem that the packaging material cannot cope with the required quality because the types and the like of the resins capable of being extrusion laminated are limited. A packaging material in which multilayers are laminated on a paper base material in order to establish the compatibility between the gas barrier property and the water vapor barrier property finds difficulty in recycling of the paper and the laminated layers. The multilayer laminated packaging material also offers a problem such that the carbon dioxide emission amount in the production thereof is large. Moreover, in the multilayer laminated packaging material, specific adhesive resins are sometimes required to be used between the respective laminated layers, to offer another problem that the production of the multilayer laminated packaging material is cumbersome.
- On the other hand, in a packaging material in which a paper base material is coated with a resin having a gas barrier property and a resin having a water vapor barrier property, the types and the like of the usable resins are scarcely limited, and various required qualities can be coped with. However, a packaging material to which both of the gas barrier property and the water vapor barrier property are imparted, for example, in the case where the moistureproof layer of Patent Literature 3 is disposed on the packaging material having a gas barrier property of Patent Literature 1 or Patent Literature 2, offers a problem that although a satisfactory water vapor barrier property is obtained, no gas barrier property is obtained. Additionally, in the case where the gas barrier layer of Patent Literature 1 or Patent Literature 2 is disposed on a moistureproof paper having the moistureproof layer of Patent Literature 3, the surface tension of the moistureproof layer, hence the gas barrier layer is not uniformly formed due to repellency, and hence no sufficient gas barrier property can be obtained.
- Accordingly, the present invention takes as its object the provision of a paper based barrier packaging material simultaneously having both of an excellent gas barrier property and an excellent water vapor barrier property.
- The main constitution of the present invention is as follows.
- 1. A paper based barrier packaging material including a plurality of coating layers disposed on a paper base material, wherein the plurality of coating layers includes a water vapor barrier layer on the paper base material and a gas barrier layer formed on the water vapor barrier layer; and in each of these coating layers, a water soluble polymer or a water suspendable polymer is used as a binder resin.
- 2. The paper based barrier packaging material according to 1., wherein the water vapor barrier layer and the gas barrier layer are different in coating material composition from each other.
- 3. The paper based barrier packaging material according to 2., wherein the binder resin of the water vapor barrier layer is a styrene-butadiene-based synthetic resin.
- 4. The paper based barrier packaging material according to 3., wherein the binder resin in the water vapor barrier layer includes kaolin having an average particle size of 5 µm or more and an aspect ratio of 10 or more.
- 5. The paper based barrier packaging material according to 4., wherein the water vapor barrier layer includes a pigment having an average particle size of 5 µm or less.
- 6. The paper based barrier packaging material according to 4., wherein the coating material forming the water vapor barrier layer includes a cross-linking agent.
- 7. The paper based barrier packaging material according to any one of 1. to 6., wherein the binder resin of the gas barrier layer is a polyvinyl alcohol resin.
- 8. The paper based barrier packaging material according to 7., wherein the gas barrier layer includes kaolin having an average particle size of 5 µm or more and an aspect ratio of 10 or more.
- 9. The paper based barrier packaging material according to 7., wherein the coating material forming the gas barrier layer includes a cross-linking agent.
- 10. The paper based barrier packaging material according to 1., wherein the coating amount of the water vapor barrier layer is 4 to 30 g/m2 in terms of dry weight and the coating amount of the gas barrier layer is 0.2 to 10 g/m2 in terms of dry weight.
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- (1) The present invention have succeeded in realizing both barrier properties, namely, a water vapor barrier and a gas barrier property, by sequentially forming by coating a water vapor barrier layer on a paper base material and further a gas barrier layer on the water vapor barrier layer. The present invention can provide a paper based barrier packaging material exhibiting an excellent gas barrier property and an excellent water vapor barrier property by forming a water vapor barrier layer and a gas barrier layer with coating layers of the coating materials using as binders polymers (aqueous coating materials) including water as dispersion media.
The coating materials forming the gas barrier layer and the water vapor barrier layer exhibit the functions to prevent the permeation of water vapor and the permeation of gas (oxygen), respectively, each in a form of a film formed by drying and solidifying. In the two types of the barrier layers, the coating layers made of the aqueous coating materials are satisfactory in the compatibility between the layers, and are strongly resistant to the interfacial separation due to the water vapor or the gas tending to permeate one of the layers from the other layer, so as to enable both functions to be satisfactorily maintained. - (2) By forming one or both of the water vapor barrier layer and the gas barrier layer by using a coating material to which, as a pigment having a large particle size, kaolin having an average particle size of 5 µm or more and an aspect ratio of 10 or more was added, the barrier property against water vapor or gas is improved.
- (3) The use of a coating material including a pigment as added thereto, having an average particle size of 5 µm or less improves the barrier property against water vapor or gas.
- (4) As the polymer for the coating layer forming the water vapor barrier layer, a styrene-butadiene-based synthetic resin is suitable. As the polymer for the coating layer forming the gas barrier layer, a polyvinyl alcohol resin is suitable. As a paper based barrier packaging material, the combination of the resins is excellent in which the coating layer mainly composed of the polyvinyl alcohol resin is formed on the coating layer, formed on a paper base material, mainly composed of the styrene-butadiene-based synthetic resin.
- (5) The styrene-butadiene synthetic resin or the polyvinyl alcohol resin including a cross-linking agent added thereto improves both barrier properties.
- The present invention is a paper based barrier packaging material (hereinafter, sometimes referred to as a "packaging material") including a water vapor barrier layer and a gas barrier layer disposed in this order on a paper base material (hereinafter, sometimes referred to as a "base paper"). The two types of the barrier layers are each formed by applying an aqueous coating material, and to the coating material, a polymer binder as a main additive, a pigment, a cross-linking agent and the like are added.
- The water vapor barrier layer or the gas barrier layer is formed by coating with a coating material including a polymer as a binder resin and using water as a dispersion medium. To the coating layers forming the two types of the barrier layers, it is preferable to add kaolin having an average particle size of 5 µm or more and an aspect ratio of 10 or more, a pigment having an average particle size of 5 µm or less, a cross-linking agent and the like.
- The reasons for the fact that the paper based barrier packaging material of the present invention including the water vapor barrier layer formed on a paper base material and further the gas barrier layer on the water vapor barrier layer simultaneously has both of an excellent water vapor barrier property and an excellent gas barrier property are inferred as follows.
- There are many instances where for the formation of the gas barrier layer, a water soluble polymer resin is used. In the case where the gas barrier layer and the water vapor barrier are disposed in this order on the paper base material, the moisture or the like in the air permeating through the paper base material operates to degrade the gas barrier layer including the water soluble polymer. On the other hand, in the case where a water vapor barrier layer including a resin satisfactory in waterproofness and a gas barrier layer are disposed in this order, the moisture passing through the paper base material is blocked by the water vapor barrier layer, and hence the moisture effect on (the degradation of) the gas barrier layer can be prevented. Accordingly, the paper based barrier packaging material of the present invention has a satisfactory water vapor barrier property and a satisfactory gas barrier property.
- The paper based barrier packaging material of the present invention is usually used in such a way that the side of the gas barrier layer is the side of the content (article to be packaged) and the side of the paper layer is the atmospheric side (outer surface). The permeation of the atmospheric moisture into the interior can be prevented, and hence when the article to be packaged is a dry substance, the structure of the present invention is effective. When a wet article is packaged, further a resin extrusion laminated layer or a film laminate layer is additionally formed on the gas barrier layer to be the inner side.
- In the present invention, the paper base material is a sheet includes pulp, a filler, and various additives. Examples of the pulp include: chemical pulps such as leaf bleached kraft pulp (LBKP), needle bleached kraft pulp (NBKP) and sulfite pulp; mechanical pulps such as stone-ground pulp and thermomechanical pulp; and non-wood fibers obtained from kenaf, bamboo, hemp and the like. These materials can be appropriately mixed to be used. Among these, the chemical pulps such as leaf bleached kraft pulp (LBKP) and needle bleached kraft pulp (NBKP) are preferable. The chemical pulps are suitable, for example, for the reasons that contamination of the base paper hardly occurs, temporal discoloration hardly occurs when used paper containers are collected as waste paper raw materials to be recycled, and chemical pulps have a high degree of whiteness to result in satisfactory surface touch at the time of printing so as to enhance the value in use as packaging materials.
- Examples of the usable filler include heretofore known fillers such as white carbon, talc, kaolin, clay, heavy calcium carbonate, precipitated calcium carbonate, titanium oxide, zeolite and synthetic resin fillers. If necessary, the following papermaking internal aids can also be used: aluminum sulfate; various anionic, cationic, nonionic, or amphoteric yield improvers; a freeness improver, a paper-strengthening agent and an internal sizing agent. Moreover, if necessary, a dye, a fluorescent whitening agent, a pH adjuster, an antifoaming agent, a pitch control agent, a slime control agent and the like can also be added.
- The method of the production (paper making) of the paper base material is not particularly limited; paper base materials can be produced by using heretofore known fourdrinier former, on-top hybrid former and gap former machines, and by performing paper making with acidic paper making, neutral paper making, alkaline paper making methods. The paper base material is preferably a material generally used for coated papers, having a basis weight of about 25 to 400 g/m2. Moreover, the surface of the paper base material can be treated with various chemicals. Examples of the chemicals to be used may include: oxidized starch, hydroxyethyl etherified starch, oxygen-modified starch, polyacrylamide, polyvinyl alcohol, a surface sizing agent, a waterproofing agent, a water retention agent, a thickener and a lubricant; these can be used each alone or in combinations of two or more thereof. The method of the surface treatment of the paper base material is not particularly limited; however, heretofore known coating apparatuses such as a rod metering size press, a pond type size press, a gate roll coater, a spray coater, a blade coater and a curtain coater can be used.
- The polymer to be used as the main component of the coating layer forming the water vapor barrier layer or the gas barrier layer is suitably a resin for which water can be used as a dispersion medium. Examples of the dosage form include a polymer aqueous solution and a form of a polymer emulsion. The polymer corresponds to the binder of the coating material for forming a coating layer.
- As the resins to be included in the water vapor barrier layer, the following resins can be used each alone or as mixtures of two or more thereof: copolymers such as styrene-butadiene-based, styrene-acrylic, ethylene-vinyl acetate-based, butadiene-methyl methacrylate-based, vinyl acetate-butyl acrylate-based copolymers; maleic anhydride copolymer; and acrylic acid-methyl methacrylate-based copolymer. Among these, styrene-butadiene-based resin is preferable from the viewpoint of the water vapor barrier property.
- In the present invention, styrene-butadiene-based synthetic resin is a resin synthesized with emulsion polymerization by using styrene and butadiene as the main constituent monomers in combination with various comonomers aiming at modification. Examples of the comonomer include: methyl methacrylate, acrylonitrile, acrylamide and hydroxyethyl acrylate; and unsaturated carboxylic acids such as itaconic acid, maleic acid and acrylic acid.
- The resins are used as emulsion-type coating materials prepared by emulsification with water as a dispersant. Examples of the emulsifier include anionic surfactants such as sodium oleate, rosin acid soap, sodium alkyl allyl sulfonate and sodium dialkyl sulfosuccinate. These can be used each alone or in combinations with nonionic surfactants. Moreover, if necessary, amphoteric or cationic surfactants may also be used.
- In the present invention, the coating material to form the water vapor barrier layer preferably does not include water-repellent components such as a hydrocarbon, a silicone-based resin, a fluorine-based resin, a fatty acid and an ester between a fatty acid and an alcohol. It is to be noted that conventional packaging materials having a water vapor barrier property are generally provided with water-repellent component-containing resins. The water-repellent component degrades the affinity between the water vapor barrier layer and the gas barrier layer, and accordingly, the moisture or gas permeating from one of these layers unpreferably promotes interfacial peeling.
- In the present invention, the inclusion of a pigment in the water vapor barrier layer improves the water vapor barrier property, and also improves the adhesion between the water vapor barrier layer and the gas barrier layer.
- Examples of the pigment include an inorganic pigment and an organic pigment. Examples of the inorganic pigment include: kaolin, clay, engineered kaolin, delaminated clay, heavy calcium carbonate, precipitated calcium carbonate, talc, titanium dioxide, barium sulfate, calcium sulfate, zinc oxide, silicic acid, silicates, colloidal silica and satin white. Examples of the organic pigment include a dense-type pigment, a hollow-type pigment, or a core-shell type pigment. These pigments can be used each alone or as mixtures of two or more thereof.
- The pigments flat in shape and large in size are suitable. The water vapor barrier property is improved by using a pigment large in particle size and a pigment small in particle size in combination.
- Among these pigments, inorganic pigments such as flat-shaped kaolin improve the water vapor barrier property. In particular, kaolin having an average particle size of 5 µm or more and an aspect ratio of 10 or more is more preferable. A flat pigment is distributed parallel to the coating layer, the water vapor permeating into the water vapor barrier layer is blocked by the flat pigment with respect to the movement in the thickness direction and is made to move in a detour so as to elongate the path of the passage of the water vapor through the water vapor barrier layer, and hence the barrier property is improved. When the aspect ratio of the added pigment is small, the number of times of detour of the water vapor in the coating layer is decreased, accordingly the distance of the movement of the water vapor is reduced, and consequently the pigment small in aspect ratio is inferior to the flat pigment having a large particle size.
- A flat pigment can be expected to have the same effect as described above on the gas barrier layer.
- As a flat pigment, in addition to kaolin, mica and montmorillonite can also be used. However, the dispersion of mica or montmorillonite is lower in concentration than the dispersion of kaolin, accordingly the coating liquid for the water vapor barrier layer using mica or montmorillonite is low in concentration so as for the pigment to find difficulty in orientation in the formed water vapor barrier layer, and hence kaolin is more suitable than mica or montmorillonite.
- By adding a pigment having an average particle size of 5 µm or less to the water vapor barrier layer, in addition to the above-described flat pigment, the water vapor barrier property can be further improved. The pigment having a small particle size is not required to be flat.
- In the present invention, from the viewpoint of the improvement of the water vapor barrier property and the adhesiveness to the gas barrier layer, it is preferable to further include a pigment having an average particle size of 5 µm or less in the water vapor barrier layer including kaolin having an average particle size of 5 µm or more and an aspect ratio of 10 or more. In this way, a structure is obtained in which a pigment having an average particle size of 5 µm or less is interposed between the kaolin particles present in a multilayered manner, having an average particle size of 5 µm or more and an aspect ratio of 10 or more, and consequently, the water vapor being forced to move along the flat plane of kaolin is blocked in its movement by the smaller pigment particles. Specifically, in the case where the pigments different in flatness and average particle size are included in the water vapor barrier layer, a state occurs in which in the water vapor barrier layer, the pigment of smaller particle size is filled in the voids formed between the adjacent flat pigment particles large in particle size, accordingly the water vapor passes all the way around the pigments, and hence the water vapor barrier layer including the pigments different in average particle size exhibits a higher water vapor barrier property as compared to the water vapor barrier layer including no pigment smaller in particle size.
- In the present invention, the mixing ratio between kaolin having an average particle size of 5 µm or more and an aspect ratio of 10 or more and the pigment having an average particle size of 5 µm or less is preferably 50/50 to 99/1 in terms of dry weight. When the ratio of kaolin having an average particle size of 5 µm or more and an aspect ratio of 10 or more is smaller than the foregoing range, the detour distance of the water vapor in the coating layer is short, and hence no sufficient water vapor barrier property can be obtained. On the other hand, the ratio of kaolin having an average particle size of 5 µm or more and an aspect ratio of 10 or more is larger than the foregoing range, the voids formed by the large particle size pigment in the coating layer cannot be sufficiently filled by the pigment having an average particle size of 5 µm or less, and hence no improvement of the water vapor barrier property is found.
- In the present invention, as the pigment having an average particle size of 5 µm or less the following pigments can be used each alone or as mixtures of two or more thereof: inorganic pigments such as kaolin, clay, engineered kaolin, delaminated clay, heavy calcium carbonate, precipitated calcium carbonate, talc, titanium dioxide, barium sulfate, calcium sulfate, zinc oxide, silicic acid, silicates, colloidal silica and satin white; and organic pigments such as a dense-type pigment, a hollow-type pigment, or a core-shell type pigment. Among these pigments, heavy calcium carbonate is preferable.
- When a pigment is included in the water vapor barrier layer, the mixing amounts of the resin and the pigment are such that a resin is used in an amount of preferably 5 to 200 parts by weight and more preferably 20 to 150 parts by weight (dry weight) in relation to 100 parts by weight (dry weight) of the pigment. In the water vapor barrier layer, it is possible to use, in addition to the resin and the pigment, various usually used aids such as a dispersant, a thickener, a water retention agent, an antifoaming agent, a waterproofing agent, a dye and a fluorescent dye.
- In the present invention, it is preferable to add a cross-linking agent typified by a multivalent metal salt to the water vapor barrier layer. The cross-linking agent causes a cross-linking reaction with the binder included in the water vapor barrier layer, and accordingly the number of the bonds (the number of the cross-linked points) in the water vapor barrier layer is increased. In other words, the water vapor barrier layer becomes dense in structure, and consequently exhibits a satisfactory water vapor barrier property.
- In the present invention, the type of the cross-linking agent is not particularly limited; the cross-linking agent appropriately according to the type of the binder included in the water vapor barrier layer from the following can be used: multivalent metal salts (the compounds produced by bonding the multivalent metals such as copper, zinc, silver, iron, potassium, sodium, zirconium, aluminum, calcium, barium, magnesium and titanium with the ionic substances such as carbonate ion, sulfate ion, nitrate ion, phosphate ion, silicate ion, nitrogen oxide and boron oxide); and amine compounds, amide compounds, aldehyde compounds, and hydroxy acids. As long as the mixing amount of the cross-linking agent allows the concentration and the viscosity of the coating material to fall within ranges permitting coating operation, the cross-linking agent can be mixed without being particularly limited with respect to the mixing amount thereof. From the viewpoint of the development of the cross-linking effect, it is preferable to use a multivalent metal salt when a styrene-based water vapor barriering resin exhibiting excellent effects in the water vapor barrier property, such as a styrene-butadiene-based resin or a styrene-acrylic-based resin is used; in particular, potassium alum is more preferable.
- The addition amount of the cross-linking agent is 1 to 10 parts by weight and more preferably 3 to 5 parts by weight in relation to 100 parts by weight of the binder resin used in the water vapor barrier layer. When the addition amount of the cross-linking agent is less than 1 part by weight, no sufficient effect is obtained, and when the addition amount of the cross-linking agent is larger than 10 parts by weight, the viscosity of the coating liquid is remarkably increased to make the coating operation difficult.
- In the present invention, when a cross-linking agent is added to the coating liquid to form the water vapor barrier layer, it is preferable to add the cross-linking agent to the coating liquid after the cross-linking agent is dissolved in a polar solvent such as ammonium hydroxide solution. By dissolving the cross-linking agent in a polar solvent, bonding occurs between the cross-linking agent and the polar solvent, and hence even when the cross-linking agent is mixed in the coating liquid, the cross-linking reaction with the latex does not occur instantly, so as to allow the thickening of the coating material to be suppressed. In this case, it is inferred that by drying after the coating operation on paper, polar solvent component is evaporated, the cross-linking reaction with the binder occurs, and the dense water vapor barrier layer is formed.
- In the present invention, the contact angle with water of the surface of the water vapor barrier layer disposed on the paper base material is preferably less than 90°, more preferably less than 85° and furthermore preferably less than 80°. When the contact angle with water is 90° or more, it is difficult to dispose a uniform gas barrier layer on the water vapor barrier layer, and it is difficult to exhibit a high gas barrier property. When the contact angle with water is less than 90°, it is possible to suppress the repulsion between the water vapor barrier layer and the gas barrier layer so as to suppress the peeling between these two layers. The contact angle serves as a measure with which the affinity between the water vapor barrier layer and the gas barrier layer is inferred.
- The method for regulating the contact angle with water of the surface of the water vapor barrier layer is not particularly limited; however, examples of such a method include a method using a resin having a low contact angle with water for the water vapor barrier layer, and a method in which a pigment or the like is added to the resin for the water vapor barrier layer.
- In the present invention, the water soluble polymer used as the binder resin of the coating material to form the gas barrier layer can be exemplified by completely saponified polyvinyl alcohol, partially saponified polyvinyl alcohol, ethylene copolymerized polyvinyl alcohol, polyvinylpyrrolidone, starch, methyl cellulose, carboxymethyl cellulose and sodium alginate. Among these, from the viewpoint of the gas barrier property, polyvinyl alcohol and carboxymethyl cellulose are preferable, and polyvinyl alcohol is furthermore preferable.
- In the present invention, examples of the pigments used in the gas barrier layer include: inorganic pigments such as kaolin, clay, engineered kaolin, delaminated clay, heavy calcium carbonate, precipitated calcium carbonate, talc, titanium dioxide, barium sulfate, calcium sulfate, zinc oxide, silicic acid, silicate, colloidal silica, satin white and mica; and organic pigments such as a dense-type pigment, a hollow-type pigment and a core-shell type pigment. These can be used each alone or as mixtures of two or more thereof. Among these, from the viewpoint of the gas barrier property, it is preferable to use an inorganic pigment.
- It is more preferable to use an inorganic pigment (in particular, kaolin) having an average particle size of 3 µm or more and an aspect ratio of 10 or more, and it is particularly preferable to use an inorganic pigment (in particular, kaolin) having an average particle size of 5 µm or more and an aspect ratio of 50 or more. When a pigment is included in the gas barrier layer, a gas such as oxygen passes around the pigment. Consequently, as compared to the gas barrier layer formed of a water soluble polymer including no pigment, the gas barrier layer formed of a water soluble polymer including a pigment has a satisfactory water vapor barrier property and an excellent gas barrier property in a high-humidity atmosphere.
- In the present invention, the mixing ratio (in terms of dry weights) between the pigment and the water soluble polymer included in the gas barrier layer is preferably such that the ratio pigment /water soluble polymer is 1/100 to 1000/100. When the proportion of the pigment falls outside the foregoing range, no sufficient gas barrier property is exhibited.
- In the present invention, it is preferable to add a cross-linking agent typified by a multivalent metal salt or the like to the gas barrier layer. The cross-linking agent bonds the hydroxyl groups in the water soluble polymer to each other through cross-linked structure, hence the amount of the hydroxyl groups having the loosened bonds (or broken bonds) when the humidity becomes high is decreased to improve the waterproofness of the whole layer, and thus the degradation of the oxygen barrier property under a high humidity can be suppressed.
- In the present invention, the type of the cross-linking agent is not particularly limited; the cross-linking agent appropriately according to the type of the binder included in the water vapor barrier layer from the following can be used: multivalent metal salts (the compounds produced by bonding the multivalent metals such as copper, zinc, silver, iron, potassium, sodium, zirconium, aluminum, calcium, barium, magnesium and titanium with the ionic substances such as carbonate ion, sulfate ion, nitrate ion, phosphate ion, silicate ion, nitrogen oxide and boron oxide); and amine compounds, amide compounds, aldehyde compounds, and hydroxy acids. As long as the mixing amount of the cross-linking agent allows the concentration and the viscosity of the coating material to fall within ranges permitting coating operation, the cross-linking agent can be mixed without being particularly limited with respect to the mixing amount thereof. From the viewpoint of the development of the cross-linking effect, it is preferable to use a multivalent metal salt and it is more preferable to use potassium alum when a styrene-based water vapor barriering resin exhibiting excellent effects in the water vapor barrier property, such as a styrene-butadiene-based resin or a styrene-acrylic-based resin is used.
- The addition amount of the cross-linking agent is 1 to 10 parts by weight and more preferably 3 to 5 parts by weight in relation to 100 parts by weight of the resin used in the gas barrier layer. When the addition amount of the cross-linking agent is less than 1 part by weight, no sufficient effect is obtained, and when the addition amount of the cross-linking agent is larger than 10 parts by weight, the viscosity of the coating liquid is remarkably increased to make the coating operation difficult.
- In the present invention, when a pigment is mixed in a water soluble polymer, it is preferable to add and mix a pigment which is water-dispersed and slurried.
- In the present invention, in the gas barrier layer, it is possible to use, in addition to the water soluble polymer and the pigment, various usually used aids such as a dispersant, a thickener, a water retention agent, an antifoaming agent, a waterproofing agent, a dye and a fluorescent dye.
- In the present invention, the coating methods of the water vapor barrier layer and the gas barrier layer are not particularly limited, and heretofore known coating apparatuses can be used. Examples of such a coating apparatus include: a blade coater, a bar coater, a roll coater, an airknife coater, a reverse roll coater, a curtain coater, a spray coater, a size press coater and a gate roll coater. As the method for drying the coating layer, usual methods using the following are used: a steam heating heater, a gas heater, an infrared heater, an electric heater, a hot air heating heater, a microwave, a cylinder dryer and the like.
- In the present invention, the coating amount of the water vapor barrier layer is preferably set at 4 to 30 g/m2, more preferably 6 to 25 g/m2 and furthermore preferably 10 to 20 g/m2 in terms of dry weight. When the coating amount is 3 g/m2 or less, there occur a problem that it is difficult for the coating liquid to perfectly coat the base paper, and hence no sufficient water vapor barrier property is obtained, and a problem that the gas barrier layer penetrates into the paper base material, and hence a uniform gas barrier property is not obtained. On the other hand, when the coating amount is 30 g/m2 or more, the drying load at the time of coating operation becomes large, unpreferably from the viewpoint of both of the operational aspect and the cost aspect.
- In the present invention, the coating amount of the gas barrier layer is preferably set at 0.2 to 10 g/m2 in terms of dry weight. When the coating amount is less than 0.2 /m2, no uniform gas barrier layer can be formed, and hence there is problem that no sufficient gas barrier property is obtained. On the other hand, the coating amount is 10 g/m2 or more, the drying load at the time of coating operation becomes large, unpreferably from the viewpoint of both of the operational aspect and the cost aspect.
- In the present invention, it is possible to dispose a sealant layer made of a polymer such as polyethylene, polypropylene or polyvinyl acetate on the paper based barrier packaging material including a water vapor barrier layer and a gas barrier layer disposed on a paper base material. The method for laminating the sealant layer is not particularly limited; it is possible to use a conventional, heretofore known methods such as a melt-extrusion lamination method, a dry lamination method using a film and a direct melt coating method.
- Hereinafter, the present invention is specifically described with reference to Examples, but of course, the present invention is not these Examples. It is to be noted that unless otherwise specified, parts and % in Examples represent parts by weight and % by weight, respectively. For the coating liquids obtained and the functional papers obtained, tests were performed on the basis of the following evaluation methods. The test results are shown in Table 1 and Table 2.
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- (1) Water vapor permeability: The water vapor permeability was measured under the conditions of a temperature of 40 ± 0.5°C and a relative humidity of 90 ± 2%, with a water vapor permeability tester (L80-4000, manufactured by Dr. Lyssy, Inc.).
- (2) Oxygen permeability: The oxygen permeability was measured with the OX-TRAN2/21, manufactured by Mocon, Inc. under the conditions of 23°C and 0% RH and the conditions of 23°C and 85% RH.
- (3) Contact angle: The surface contact angle after an elapsed time of 0.1 second from the dropping of a drop of water was measured in an atmosphere of 23°C and 50% RH, with a dynamic surface contact angle measurement apparatus (Dynamic Absorption and Contact Angle Tester DAT1100, manufactured by Fibro System AB).
- (4) Average particle size: A sample slurry was dropwise mixed in a pure water including 0.2% by weight of sodium hexametaphosphate added as a dispersant to prepare a uniform dispersion, and the particle size of the sample was measured by using the resulting dispersion with a laser particle size analyzer (Mastersizer Type S, manufactured by Malvern Instruments Ltd.).
- (5) Aspect ratio: The images of a pigment in the planar direction and the cross-sectional direction of the pigment were photographed with a SEM (scanning electron microscope), and the diameter and the length of the pigment orientation plane were measured and the aspect ratio was derived with the relation [aspect ratio = diameter/thickness of the pigment orientation plane].
- A raw material pulp was prepared by mixing, with a weight ratio of 80/20, a leaf bleached kraft pulp (LBKP) having a Canadian standard freeness (CSF) of 500 ml and a needle bleached kraft pulp (NBKP) having a CSF of 530 ml. To a raw material pulp slurry, polyacrylamide (PAM) having a molecular weight of 2,500,000 as a dry paper-strengthening agent in an amount of 0.1% in relation to the bone-dry weight of the pulp, alkyl ketene dimer (AKD) as sizing agent in an amount of 0.35% in relation to the bone-dry weight of the pulp, a polyamide epichlorohydrin (PAEH)-based resin as a wet paper-strengthening agent in an amount of 0.15% in relation to the bone-dry weight of the pulp, and further polyacrylamide (PAM) having a molecular weight of 10,000,000 as a yield improver in an amount of 0.08% in relation to the bone-dry weight of the pulp were added; and then paper making was performed with a duo former FM-type paper making machine at a rate of 300 m/min to yield a paper having a basis weight of 59 g/m2. Next, both faces of the obtained paper were coated with polyvinyl alcohol (PVA117, manufactured by Kuraray Co., Ltd.) regulated to a solid content concentration of 2% in an amount of 1.0 g/m2 by using a rod metering size press, and dried to yield a base paper having a basis weight of 60 g/m2. The base paper obtained was subjected to a smoothing treatment with a chilled calender at a rate of 300 min/m and at a linear load of 50 kgf/cm, in a single pass.
- To large particle size engineered kaolin (Barrisurf HX, particle size: 9.0 µm, aspect ratio: 80-100, manufactured by Imerys Minerals Ltd.), sodium polyacrylate was added as a dispersant (in an amount of 0.2 part in relation to inorganic pigment), and the resulting mixture was dispersed with a Serie mixer to prepare a large particle size kaolin slurry having a solid content concentration of 55%. In the kaolin slurry obtained, a styrene-butadiene-based latex (PNT7868, manufactured by Zeon Corp.) was mixed in an amount of 100 parts (solid content) in relation to the pigment to yield a coating liquid A having a solid content concentration of 50%.
- Polyvinyl alcohol (PVA117, manufactured by Kuraray Co., Ltd.) was regulated so as to have a solid content concentration of 10% to yield a coating liquid B.
- The base paper obtained was single-side coated with the coating liquid A so as to have a coating amount (dry amount) of 12 g/m2 at a coating speed of 300 m/min with a blade coater and dried; subsequently, the coated side was single-side coated with the coating liquid B so as to have a coating amount (dry amount) of 2.0 g/m2 at a coating speed of 300 m/min with a roll coater to yield a paper based barrier packaging material.
- In the coating liquid for the oxygen barrier layer, to the large particle size engineered kaolin (Barrisurf HX, manufactured by Imerys Minerals Ltd.), sodium polyacrylate was added as a dispersant (in an amount of 0.2 part in relation to the inorganic pigment), and the resulting mixture was dispersed with a Serie mixer to prepare a large particle size kaolin slurry having a solid content concentration of 55%. A paper based barrier packaging material was obtained in the same manner as in Example 1 except that a coating liquid was used which was prepared by mixing the obtained kaolin slurry and the coating liquid B in a ratio of pigment:coating liquid B = 100:100 in terms of the solid content so as for the solid content concentration to be 10%.
- A paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the oxygen barrier layer, potassium alum (aluminum potassium sulfate dodecahydrate, manufactured by Kanto Chemical Co., Inc.) was dissolved so as for the concentration to be 5%, the obtained potassium alum aqueous solution was mixed in an amount of 3 parts in terms of the solid content in relation to polyvinyl alcohol, to prepare a coating liquid having a solid content concentration of 10%, and the thus obtained coating liquid was used.
- A paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the oxygen barrier layer, the kaolin slurry prepared in Example 2 was mixed in the coating liquid B in a ratio of pigment:coating liquid B = 100:100 in terms of the solid content, and further the potassium alum aqueous solution dissolved in Example 3 was mixed in an amount of 3 parts in terms of the solid content in relation to polyvinyl alcohol, to prepare a coating liquid having a solid content concentration of 10%, and the thus obtained coating liquid was used.
- A paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the water vapor barrier layer, a coating liquid in which a heavy calcium carbonate slurry (FMT-75, average particle size: 1.6 µm, aspect ratio: 1, manufactured by Fimatec Ltd.) was mixed in and stirred with the pigment of the coating liquid A so as for the pigment mixing ratio to be 75:25 was used.
- A paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the water vapor barrier layer, the potassium alum aqueous solution dissolved in Example 3 was mixed in an amount of 3 parts in relation to the pigment in the coating liquid obtained in Example 5 to prepare a coating liquid having a solid content concentration of 50%, and the thus obtained coating liquid was used.
- A paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the oxygen barrier layer, the coating liquid obtained in Example 4 was used, and in the coating liquid for the water vapor barrier layer, the coating liquid obtained in Example 5 was used.
- A paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the oxygen barrier layer, the coating liquid obtained in Example 4 was used, and in the coating liquid for the water vapor barrier layer, the coating liquid obtained in Example 6 was used.
- A paper based barrier packaging material was obtained in the same manner as in Example 2 except that in the coating liquid for the oxygen barrier layer, the large particle size engineered kaolin in the coating liquid obtained in Example 2 was altered to mica (B-82, particle size: 180 µm, manufactured by Matsuo Sangyo Co., Ltd.).
- A paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the oxygen barrier layer, the large particle size engineered kaolin in the coating liquid obtained in Example 1 was altered to montmorillonite (Nikka Knight A-36, particle size: 400 µm, manufactured by Toshin Chemicals Co., Ltd.).
- A paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the water vapor barrier layer, the large particle size engineered kaolin in the coating liquid obtained in Example 1 was altered to mica (B-82, particle size: 180 µm, manufactured by Matsuo Sangyo Co., Ltd.), the pigment dispersion concentration was altered to 20%, and the coating liquid concentration was altered to 30.
- A paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the water vapor barrier layer, the large particle size engineered kaolin in the coating liquid obtained in Example 1 was altered to montmorillonite (Nikka Knight A-36, particle size: 400 µm, manufactured by Toshin Chemicals Co., Ltd.), the pigment dispersion concentration was altered to 20%, the coating liquid concentration was altered to 30%, and the coating amount was altered to 9 g/m2.
- A paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the water vapor barrier layer, the styrene-butadiene-based latex in Example 1 was altered to an acrylic-styrene-based copolymer emulsion (Saivinol X-511-374E, manufactured by Saiden Chemical Industry Co., Ltd.).
- A paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the water vapor barrier layer, the latex was altered to a styrene-butadiene-based latex (L7360, manufactured by Asahi Kasei Chemicals Corp.).
- A paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the water vapor barrier layer, the pigment used in the coating liquid was altered from the large particle size engineered kaolin (Barrisurf HX, manufactured by Imerys Minerals Ltd.) to the large particle size engineered kaolin (Capim CC, particle size: 8.0 µm, aspect ratio: 10 to 15, manufactured by Imerys Minerals Ltd.).
- A paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the water vapor barrier layer, the pigment used in the coating liquid was altered from the large particle size engineered kaolin (Barrisurf HX, manufactured by Imerys Minerals Ltd.) to a fine particle kaolin (Hydragloss, average particle size: 0.3 µm, aspect ratio: 10 to 15, manufactured by KaMin LLC).
- A paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the water vapor barrier layer, the pigment used in the coating liquid was altered from the large particle size engineered kaolin (Barrisurf HX, manufactured by Imerys Minerals Ltd.) to a second grade kaolin (KCS, average particle size: 3.6 µm, aspect ratio: 10 to 15, manufactured by Imerys Minerals Ltd.).
- A paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the water vapor barrier layer, the latex used in the coating liquid was altered to a styrene-butadiene-based latex (PNT7889, manufactured by ZEON Corp.).
- A paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the water vapor barrier layer, the latex used in the coating liquid was altered to a styrene-butadiene-based latex (L7360, Asahi Kasei Chemicals Corp.).
- A paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the water vapor barrier layer, the latex used in the coating liquid was altered to an acrylic copolymer latex (E316, manufactured by Asahi Kasei Chemicals Corp.).
- A paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the coating liquid for the water vapor barrier layer, the latex used in the coating liquid was altered to an acrylic copolymer aqueous emulsion (EK-61, manufactured by Saiden Chemical Industry Co., Ltd.).
- A paper based barrier packaging material was obtained in the same manner as in Example 1 except that the coating amount of the coating liquid A was altered from 12 g/m2 to 6 g/m2 in terms of dry weight.
- A paper based barrier packaging material was obtained in the same manner as in Example 1 except that the coating amount of the coating liquid A was altered from 12 g/m2 to 15 g/m2 in terms of dry weight.
- A paper based barrier packaging material was obtained in the same manner as in Example 1 except that the coating amount of the coating liquid B was altered from 2 g/m2 to 1 g/m2 in terms of dry weight.
- A paper based barrier packaging material was obtained in the same manner as in Example 1 except that the coating amount of the coating liquid B was altered from 2 g/m2 to 4 g/m2 in terms of dry weight.
- A paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the preparation of the coating liquid for the water vapor barrier layer, the mixing amount of the styrene-butadiene-based latex (PNT7868, manufactured by ZEON Corp.) was altered from 100 parts to 50 parts (solid content) in relation to the pigment.
- A paper based barrier packaging material was obtained in the same manner as in Example 1 except that in the preparation of the coating liquid for the water vapor barrier layer, the mixing amount of the styrene-butadiene-based latex (PNT7868, manufactured by ZEON Corp.) was altered from 100 parts to 150 parts (solid content) in relation to the pigment.
- A paper based barrier packaging material was obtained in the same manner as in Example 2 except that in the preparation of the coating liquid for the oxygen barrier layer, the mixing amount of the kaolin slurry was altered in such a way that the ratio in terms of the solid content was altered from pigment:coating liquid B = 100:100 to 150:100.
- A paper based barrier packaging material was obtained in the same manner as in Example 2 except that in the preparation of the coating liquid for the oxygen barrier layer, the mixing amount of the kaolin slurry was altered in such a way that the ratio in terms of the solid content was altered from pigment:coating liquid B = 100:100 to 50:100.
- A paper based barrier packaging material was obtained in the same manner as in Example 1 except that the gas barrier layer and the water vapor barrier layer were disposed in this order on the paper base material.
- A paper based barrier packaging material was obtained in the same manner as in Example 1 except that no water vapor barrier layer was disposed.
- A paper based barrier packaging material was obtained in the same manner as in Example 1 except that no gas barrier layer was disposed.
[Table 1] Coating amount of water vapor barrier layer Contact angle after coating of water vapor barrier layer Water vapor permeability Coating amount of oxygen barrier layer Oxygen permeability (under dry condition) Oxygen permeability (under high humidity) g/m2 ∘ g/m2·day g/m2 g/m2·day g/m2·day Example 1 12.0 75 250 2.0 1.0 200 Example 2 12.0 75 250 2.0 1.0 80 Example 3 12.0 75 250 2.0 1.0 150 Example 4 12.0 75 250 2.0 1.0 50 Example 5 12.0 75 200 2.0 1.0 200 Example 6 12.0 75 150 2.0 1.0 200 Example 7 12.0 75 200 2.0 1.0 50 Example 8 12.0 75 150 2.0 1.0 50 Example 9 12.0 75 250 2.0 1.0 80 Example 10 12.0 75 250 2.0 1.0 80 Example 11 9.0 75 300 2.0 1.0 200 Example 12 9.0 75 300 2.0 1.0 200 Example 13 12.0 90 250 2.0 1.0 300 Example 14 12.0 80 250 2.0 1.0 250 [Table 2] Coating amount of water vapor barrier layer Contact angle after coating of water vapor barrier layer Water vapor permeability Coating amount of oxygen barrier layer Oxygen permeability (under dry condition) Oxygen permeability (under high humidity) g/m2 ∘ g/m2·day g/m2 g/m2·day g/m2·day Example 15 12.0 75 280 2.0 1.0 220 Example 16 12.0 75 380 2.0 1.0 320 Example 17 12.0 75 330 2.0 1.0 280 Example 18 12.0 75 260 2.0 1.0 200 Example 19 12.0 75 250 2.0 1.0 200 Example 20 12.0 80 300 2.0 1.0 240 Example 21 12.0 80 300 2.0 1.0 240 Example 22 7.0 70 350 2.0 1.0 300 Example 23 15.0 75 200 2.0 1.0 150 Example 24 12.0 75 250 1.0 2.0 250 Example 25 12.0 75 250 3.0 0.5 150 Example 26 12.0 70 280 2.0 1.0 220 Example 27 12.0 80 220 2.0 1.0 180 Example 28 12.0 75 250 2.0 2.0 150 Example 29 12.0 75 250 2.0 0.5 230 Comparative Example 1 12.0 75 250 2.0 10000↑ 10000↑ Comparative Example 2 - - 10000↑ 2.0 1.0 10000↑ Comparative Example 3 12.0 75 250 - 10000↑ 10000↑ - From the test data of Examples and Comparative Examples, the following properties can be listed.
- (1) From the data of Example 1 and Comparative Examples 1, 2 and 3, it can be seen that Example 1 in which a water vapor barrier layer was formed on a paper base material and further a gas barrier layer was formed on the water vapor barrier layer is low in water vapor permeability and oxygen permeability. In contrast, in Comparative Example 2 in which only the gas barrier layer is disposed, the oxygen permeability and the water vapor permeability are extremely large, and both of these barrier property functions are not exhibited; in Comparative Example 3 in which only the water vapor barrier layer is disposed and Comparative Example 1 in which the water vapor barrier layer is disposed on the gas barrier layer, the water vapor barrier property exhibits the same degree of function as in Example 1, but the gas barrier property is not observed at all. This shows the result that the moisture permeating the paper base material degraded the gas barrier layer. Accordingly, this shows the result clearly demonstrating the usefulness of the present invention in which the water vapor barrier layer is disposed on the paper base material, and further the gas barrier layer is disposed on the water vapor barrier layer.
- (2) In Examples 6 and 8 in each of which potassium alum, a cross-linking agent, was added to the coating material for the water vapor barrier layer, the water vapor barrier property is more improved than Example 1.
- (3) In Examples 5 and 7 in each of which large and small pigments, namely, large particle size kaolin having a large flatness and heavy calcium carbonate fine particles were used in combination in the coating material for the water vapor barrier layer, the water vapor barrier property is more improved than in Example 1.
- (4) It has been able to be verified that kaolin, mica (Example 11) and montmorillonite (Example 12), which are large particle size pigments having an aspect ratio of 80 or more, are effective; in particular, kaolin having a large particle size and an aspect ratio of 80 or more exhibited a more excellent water vapor barrier property than other pigments.
- (5) From the results of Examples 2, 3, 4, 7, 8, 9 and 10 in which large particle size kaolin, mica and montmorillonite (these are large particle size pigments) and calcium alum (cross-linking agent) were used each alone or in combination in the gas barrier layer, it is possible to suppress the degradation of the gas barrier property performance to a small extent in a high humidity environment.
- (6) In the cases where the contact angle of a water drop on the water vapor barrier layer is 90 degrees (Example 13) or 80 degrees (Examples 14, 21 and 22), to be larger than the contact angles of a water drop of 75 degrees in Example 1 and the like, the degradation of the gas barrier property performance becomes somewhat larger in a high humidity environment, and accordingly the smaller the contact angle of a water drop, the more effectively the degradation of the gas barrier property performance due to the humidity change can be prevented.
- (7) The results of Examples 1, 15, 16 and 17 reveals a tendency of the water vapor barrier performance to depend on the particles size of the pigment added to the water vapor barrier layer. The gas barrier performance in a high humidity environment also shows a similar dependence on the particle size.
- (8) The results of Examples 1, 14, 18, 19, 20 and 21 has verified that as the binder resin used in the coating material to form the water vapor barrier layer, the styrene-butadiene-based copolymer and the acrylic copolymer are useful.
- (9) It has been able to be verified that the coating amount (dry weight) of the water vapor barrier layer falling within a range from 6 to 15g/m2 and the coating amount (dry weight) of the gas barrier layer falling within a range from 1 to 4 g/m2 allow a sufficient water vapor barrier property and a sufficient gas barrier property to be exhibited, respectively.
Claims (10)
- A paper based barrier packaging material comprising a plurality of coating layers disposed on a paper base material, wherein the plurality of coating layers includes a water vapor barrier layer on the paper base material and a gas barrier layer formed on the water vapor barrier layer; and in each of these coating layers, a water soluble polymer or a water suspendable polymer is used as a binder resin.
- The paper based barrier packaging material according to claim 1, wherein the water vapor barrier layer and the gas barrier layer are different in coating material composition from each other.
- The paper based barrier packaging material according to claim 2, wherein the binder resin of the water vapor barrier layer is a styrene-butadiene-based synthetic resin.
- The paper based barrier packaging material according to claim 3, wherein the binder resin in the water vapor barrier layer includes kaolin having an average particle size of 5 µm or more and an aspect ratio of 10 or more.
- The paper based barrier packaging material according to claim 4, wherein the water vapor barrier layer includes a pigment having an average particle size of 5 µm or less.
- The paper based barrier packaging material according to claim 4, wherein the coating material forming the water vapor barrier layer includes a cross-linking agent.
- The paper based barrier packaging material according to any one of claims 1 to 6, wherein the binder resin of the gas barrier layer is a polyvinyl alcohol resin.
- The paper based barrier packaging material according to claim 7, wherein the gas barrier layer includes kaolin having an average particle size of 5 µm or more and an aspect ratio of 10 or more.
- The paper based barrier packaging material according to claim 7, wherein the coating material forming the gas barrier layer includes a cross-linking agent.
- The paper based barrier packaging material according to claim 1, wherein the coating amount of the water vapor barrier layer is 4 to 30 g/m2 in terms of dry weight and the coating amount of the gas barrier layer is 0.2 to 10 g/m2 in terms of dry weight.
Applications Claiming Priority (7)
Application Number | Priority Date | Filing Date | Title |
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JP2011246162 | 2011-11-10 | ||
JP2012002671 | 2012-01-11 | ||
JP2012002670 | 2012-01-11 | ||
JP2012011279 | 2012-01-23 | ||
JP2012032254 | 2012-02-17 | ||
JP2012120377 | 2012-05-28 | ||
PCT/JP2012/079176 WO2013069788A1 (en) | 2011-11-10 | 2012-11-09 | Barrier paper packaging material |
Publications (3)
Publication Number | Publication Date |
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EP2777934A1 true EP2777934A1 (en) | 2014-09-17 |
EP2777934A4 EP2777934A4 (en) | 2015-07-01 |
EP2777934B1 EP2777934B1 (en) | 2017-03-15 |
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EP12847115.8A Active EP2777934B1 (en) | 2011-11-10 | 2012-11-09 | Barrier paper packaging material |
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EP (1) | EP2777934B1 (en) |
JP (1) | JP5331265B1 (en) |
CN (1) | CN104080607B (en) |
WO (1) | WO2013069788A1 (en) |
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Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0764739B1 (en) * | 1995-09-22 | 2001-01-24 | Oji Paper Co., Ltd. | Moisture-proof paper sheet |
JP2000177244A (en) * | 1998-12-11 | 2000-06-27 | Fuji Photo Film Co Ltd | Thermal recording material |
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-
2012
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- 2012-11-09 CN CN201280054858.5A patent/CN104080607B/en active Active
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- 2012-11-09 JP JP2013505656A patent/JP5331265B1/en active Active
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Also Published As
Publication number | Publication date |
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CN104080607A (en) | 2014-10-01 |
CN104080607B (en) | 2016-11-09 |
WO2013069788A1 (en) | 2013-05-16 |
JPWO2013069788A1 (en) | 2015-04-02 |
JP5331265B1 (en) | 2013-10-30 |
EP2777934B1 (en) | 2017-03-15 |
EP2777934A4 (en) | 2015-07-01 |
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