JP2008087765A - Heat insulating paper-made container, and raw material sheet used for the same - Google Patents
Heat insulating paper-made container, and raw material sheet used for the same Download PDFInfo
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- JP2008087765A JP2008087765A JP2006266907A JP2006266907A JP2008087765A JP 2008087765 A JP2008087765 A JP 2008087765A JP 2006266907 A JP2006266907 A JP 2006266907A JP 2006266907 A JP2006266907 A JP 2006266907A JP 2008087765 A JP2008087765 A JP 2008087765A
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- paper
- thermoplastic resin
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- 239000002994 raw material Substances 0.000 title claims abstract description 38
- 239000012611 container material Substances 0.000 title 1
- 229920005992 thermoplastic resin Polymers 0.000 claims abstract description 102
- 239000000463 material Substances 0.000 claims abstract description 27
- 238000010438 heat treatment Methods 0.000 claims abstract description 23
- 238000001704 evaporation Methods 0.000 claims abstract description 10
- 239000006260 foam Substances 0.000 claims description 22
- 239000000758 substrate Substances 0.000 claims description 17
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 11
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 11
- 239000011248 coating agent Substances 0.000 claims description 10
- 238000000576 coating method Methods 0.000 claims description 10
- 229920002472 Starch Polymers 0.000 claims description 9
- 235000019698 starch Nutrition 0.000 claims description 9
- 239000008107 starch Substances 0.000 claims description 8
- 230000008020 evaporation Effects 0.000 claims description 6
- 238000005187 foaming Methods 0.000 abstract description 31
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 30
- 238000009413 insulation Methods 0.000 abstract description 17
- 238000002803 maceration Methods 0.000 abstract 1
- 239000000123 paper Substances 0.000 description 225
- 239000010410 layer Substances 0.000 description 107
- 239000002585 base Substances 0.000 description 88
- 238000004519 manufacturing process Methods 0.000 description 52
- 238000000034 method Methods 0.000 description 33
- 239000002655 kraft paper Substances 0.000 description 20
- 238000002844 melting Methods 0.000 description 18
- 230000008018 melting Effects 0.000 description 17
- 239000000835 fiber Substances 0.000 description 16
- 229920005989 resin Polymers 0.000 description 15
- 239000011347 resin Substances 0.000 description 15
- 239000011121 hardwood Substances 0.000 description 14
- 238000010030 laminating Methods 0.000 description 11
- 238000004513 sizing Methods 0.000 description 11
- 239000003795 chemical substances by application Substances 0.000 description 10
- 238000002156 mixing Methods 0.000 description 10
- 229920001131 Pulp (paper) Polymers 0.000 description 9
- 239000012756 surface treatment agent Substances 0.000 description 9
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 8
- 238000003475 lamination Methods 0.000 description 8
- 230000002378 acidificating effect Effects 0.000 description 7
- 238000010009 beating Methods 0.000 description 7
- 238000001125 extrusion Methods 0.000 description 7
- 239000000945 filler Substances 0.000 description 7
- 230000008014 freezing Effects 0.000 description 7
- 238000007710 freezing Methods 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- -1 sulfuric acid band Chemical class 0.000 description 7
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 6
- 239000004698 Polyethylene Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 229920001684 low density polyethylene Polymers 0.000 description 6
- 239000004702 low-density polyethylene Substances 0.000 description 6
- 229920001179 medium density polyethylene Polymers 0.000 description 6
- 239000004701 medium-density polyethylene Substances 0.000 description 6
- 230000007935 neutral effect Effects 0.000 description 6
- 239000000654 additive Substances 0.000 description 5
- 238000000465 moulding Methods 0.000 description 5
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- 230000008569 process Effects 0.000 description 5
- 239000011122 softwood Substances 0.000 description 5
- 238000004804 winding Methods 0.000 description 5
- 229910052782 aluminium Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 4
- 230000007613 environmental effect Effects 0.000 description 4
- 239000004794 expanded polystyrene Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 241000218631 Coniferophyta Species 0.000 description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 3
- 229920002522 Wood fibre Polymers 0.000 description 3
- 229910000019 calcium carbonate Inorganic materials 0.000 description 3
- 210000004027 cell Anatomy 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 239000011888 foil Substances 0.000 description 3
- 229920001903 high density polyethylene Polymers 0.000 description 3
- 239000004700 high-density polyethylene Substances 0.000 description 3
- 229920000092 linear low density polyethylene Polymers 0.000 description 3
- 239000004707 linear low-density polyethylene Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 229920003002 synthetic resin Polymers 0.000 description 3
- 239000000057 synthetic resin Substances 0.000 description 3
- 229920003169 water-soluble polymer Polymers 0.000 description 3
- 239000002025 wood fiber Substances 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 2
- 229920006127 amorphous resin Polymers 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 229920006038 crystalline resin Polymers 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000011049 filling Methods 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000001254 oxidized starch Substances 0.000 description 2
- 235000013808 oxidized starch Nutrition 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920002401 polyacrylamide Polymers 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920000768 polyamine Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 239000002356 single layer Substances 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 241000609240 Ambelania acida Species 0.000 description 1
- 229920008790 Amorphous Polyethylene terephthalate Polymers 0.000 description 1
- 240000006248 Broussonetia kazinoki Species 0.000 description 1
- 235000006716 Broussonetia kazinoki Nutrition 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-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
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 241001265525 Edgeworthia chrysantha Species 0.000 description 1
- 240000000797 Hibiscus cannabinus Species 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229930182556 Polyacetal Natural products 0.000 description 1
- 229920002873 Polyethylenimine Polymers 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 229920001938 Vegetable gum Polymers 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 239000004840 adhesive resin Substances 0.000 description 1
- 229920006223 adhesive resin Polymers 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- ANBBXQWFNXMHLD-UHFFFAOYSA-N aluminum;sodium;oxygen(2-) Chemical compound [O-2].[O-2].[Na+].[Al+3] ANBBXQWFNXMHLD-UHFFFAOYSA-N 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 239000010905 bagasse Substances 0.000 description 1
- AYJRCSIUFZENHW-DEQYMQKBSA-L barium(2+);oxomethanediolate Chemical compound [Ba+2].[O-][14C]([O-])=O AYJRCSIUFZENHW-DEQYMQKBSA-L 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000002981 blocking agent Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 210000002421 cell wall Anatomy 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 238000003851 corona treatment Methods 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000035622 drinking Effects 0.000 description 1
- 238000009820 dry lamination Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 235000013410 fast food Nutrition 0.000 description 1
- 239000011790 ferrous sulphate Substances 0.000 description 1
- 235000003891 ferrous sulphate Nutrition 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 239000002803 fossil fuel Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 235000015220 hamburgers Nutrition 0.000 description 1
- 230000017525 heat dissipation Effects 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 235000008446 instant noodles Nutrition 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- RUTXIHLAWFEWGM-UHFFFAOYSA-H iron(3+) sulfate Chemical compound [Fe+3].[Fe+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O RUTXIHLAWFEWGM-UHFFFAOYSA-H 0.000 description 1
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 1
- 229910000360 iron(III) sulfate Inorganic materials 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 239000010813 municipal solid waste Substances 0.000 description 1
- 235000012149 noodles Nutrition 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000012766 organic filler Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000013054 paper strength agent Substances 0.000 description 1
- 239000010893 paper waste Substances 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000011116 polymethylpentene Substances 0.000 description 1
- 229920000306 polymethylpentene Polymers 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920013636 polyphenyl ether polymer Polymers 0.000 description 1
- 229920001955 polyphenylene ether Polymers 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 229910001388 sodium aluminate Inorganic materials 0.000 description 1
- 235000014347 soups Nutrition 0.000 description 1
- 230000001360 synchronised effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 238000009816 wet lamination Methods 0.000 description 1
- UGZADUVQMDAIAO-UHFFFAOYSA-L zinc hydroxide Chemical compound [OH-].[OH-].[Zn+2] UGZADUVQMDAIAO-UHFFFAOYSA-L 0.000 description 1
- 229940007718 zinc hydroxide Drugs 0.000 description 1
- 229910021511 zinc hydroxide Inorganic materials 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Packages (AREA)
- Wrappers (AREA)
- Laminated Bodies (AREA)
Abstract
Description
本発明は、断熱性を必要とする紙製容器及び容器用の原材料シートに関する。さらに詳細には、自動販売機等に利用されるホットコーヒーなどの充填用のカップ、熱湯を注入することによって内填物を飲食し得る状態にするいわゆる即席可食品用容器、さらには電子レンジによる調理用の容器等に利用される断熱性を有する使い捨て容器に関する。 The present invention relates to a paper container requiring heat insulation and a raw material sheet for the container. More specifically, a cup for filling hot coffee or the like used in vending machines, a so-called instant food container that makes it possible to eat and drink the contents by injecting hot water, and a microwave oven The present invention relates to a disposable container having heat insulation used for a cooking container or the like.
ハンバーガーショップなどのファーストフード店や列車の車内あるいは自動販売機などでコーヒーあるいはスープなどの温飲料が購入者に供される場合、およびカップ入り即席ラーメンなどでは一般的に断熱容器が使用されている。
従来、このような用途に使用される容器としては、発泡ポリスチレン(EPS)製の断熱性を有するものが知られている。これはポリスチレンに発泡剤を加える工程を経た後、この材料をモールド内に注型し、その後、熱と圧力を加えて原料を発泡させ、成型容器を型から取り出すことによって製造される。このようにして得られた断熱性容器は断熱性の点では非常に優れている。しかし、この容器は全体のプラスチックを発泡させていることから嵩があり、ゴミ量が多くなる。そして、使用後にゴミとして焼却処分する際、高熱を発して燃焼するため焼却炉を損傷しやすく、石油資源の節約の観点からも見直しが求められている。また、環境ホルモンとしての人体への悪影響も懸念される、さらに、発泡ポリスチレンの外表面は微小な凹凸が多数存在するので、外表面に模様、文字、記号などを印刷しても鮮明に表現されない、紙カップに比べ肉厚強度が弱く即席麺などの比較的大きな容器の場合輸送中に割れたりすることがある、など欠点もあった。
Insulated containers are generally used when fast drinks such as coffee or soup are provided to buyers in fast food stores such as hamburger shops, trains, vending machines, and instant ramen in cups. .
Conventionally, as a container used for such a use, what has the heat insulation property made from expanded polystyrene (EPS) is known. This is manufactured by adding a foaming agent to polystyrene, then casting this material into a mold, then applying heat and pressure to foam the raw material, and removing the molding container from the mold. The heat insulating container thus obtained is very excellent in terms of heat insulating properties. However, this container is bulky because the entire plastic is foamed, and the amount of dust increases. And, when incinerated as garbage after use, the incinerator is easily damaged because it emits high heat and it is required to be reviewed from the viewpoint of saving petroleum resources. In addition, there are concerns about adverse effects on the human body as environmental hormones. Furthermore, since the outer surface of expanded polystyrene has many minute irregularities, even if patterns, letters, symbols, etc. are printed on the outer surface, they are not clearly expressed. In addition, the thickness of the container is weaker than that of a paper cup, and in the case of a relatively large container such as instant noodles, the container may be broken during transportation.
一方、前記の発泡プラスチック製容器の他に、例えば、特許文献1(特開昭57−110439号公報)には、容器胴部材及び底板部材からなる紙製容器において、容器胴部材の外壁面に低融点の熱可塑性合成樹脂フィルムをラミネートし、加熱することにより、基材である紙に含まれている水分の蒸気圧を利用してフィルムを凹凸に発泡させる技術が記載されている。このとき、紙の他面には、加熱時に蒸気圧を保持する層として、同様の発泡層となる熱可塑性合成樹脂フィルムをラミネートするか、又は、アルミ箔をコーティグすることが記載されている。この容器は比較的良好な断熱性を有し、安価に、かつ、容易に製造することができるなどの利点を有する。
同じく、紙に含有されている水分の加熱蒸発により発泡させる技術として、特許文献2(特許第3596681号公報)には、胴部材の一方の壁面に、紙の表面側から低融点の熱可塑性樹脂の発泡内層とこれよりも高い融点を有する熱可塑性樹脂の非発泡外層とからなる2層構造断熱膜が被着されており、発泡内層と紙との層間強度、紙の坪量、発泡層および非発泡外層の膜厚を規定した紙製容器が記載されている。特許文献2にはまた、紙の他面に、加熱時に蒸気圧を保持する層として高融点の熱可塑性樹脂をラミネートすることが記載されている。
また、特許文献3には、容器胴部材の開口上縁に上部フランジ部を有する紙製容器が記載されており、フランジ部を断面角形に強制加工することにより、フランジ部が発泡せず、口当たりが良くなることが記載されている。さらに、フランジ部の内側巻き込み端をフランジ部の上部に重合させて二重構造にすることにより、強度が高まることなどが記載されている。
On the other hand, in addition to the above-mentioned foamed plastic container, for example, Patent Document 1 (Japanese Patent Laid-Open No. 57-110439) discloses a paper container composed of a container body member and a bottom plate member on the outer wall surface of the container body member. A technique is described in which a low-melting thermoplastic synthetic resin film is laminated and heated to foam the film into irregularities using the vapor pressure of moisture contained in the paper that is the base material. At this time, it is described that the other surface of the paper is laminated with a thermoplastic synthetic resin film that becomes a similar foamed layer or coated with an aluminum foil as a layer for maintaining the vapor pressure during heating. This container has a comparatively good heat insulating property, and has advantages such as being inexpensive and easy to manufacture.
Similarly, as a technique for foaming by heating and evaporation of moisture contained in paper, Patent Document 2 (Patent No. 3596681) discloses a thermoplastic resin having a low melting point on one wall surface of the body member from the surface side of the paper. And a non-foamed outer layer of a thermoplastic resin having a higher melting point than that of the inner layer of the foamed inner layer. The interlayer strength between the foamed inner layer and the paper, the basis weight of the paper, the foamed layer and A paper container that defines the thickness of the non-foamed outer layer is described. Patent Document 2 also describes laminating a thermoplastic resin having a high melting point as a layer for maintaining the vapor pressure during heating on the other side of the paper.
Patent Document 3 describes a paper container having an upper flange portion at the upper edge of the opening of the container body member. By forcibly processing the flange portion into a square cross section, the flange portion does not foam, and the mouth feels. Is described as improving. Furthermore, it describes that the strength is increased by superposing the inner winding end of the flange part on the upper part of the flange part to form a double structure.
特許文献1あるいは2に記載の容器は、紙を基材とし、ラミネート層(樹脂層)は石油を原料に作られているもののその厚さは断熱性に必要な最小限に抑えられている。そのため、化石燃料の使用が極力削減されており、全体が発泡ポリスチレンからなる容器に比べて環境負荷が小さく、また印刷性にも優れる。
しかし、紙基材中に含まれていた水分を加熱蒸発させ、この蒸発水分により熱可塑性樹脂層を発泡させて断熱性を付与する機構であることから、紙中の水分が少ないと発泡が不十分となり、十分に発泡しないと高い断熱性は得られない。そして、坪量の低い紙は含水量が小さく発泡性に劣るため、紙基材としては高坪量のものを使用しなければならない。
一方、紙製容器は、胴部材と底板部材とからカップの形に成型したり、特に容器胴部材の開口上縁には、飲食する際の口当たりや強度付与のため特許文献3のように上部フランジ部が設けられるが、坪量の高い紙を用いた場合は成型加工しにくく、また、全体のコストアップも招く。さらに、容器が軽量であると輸送面やリサイクルの面から有利であり、紙の坪量は低いことが望ましい。
そこで、本発明は、紙の坪量を高くすることなく、十分な発泡性が得られ断熱性に優れる紙製容器を提供することを目的とする。
The container described in Patent Document 1 or 2 uses paper as a base material, and the laminate layer (resin layer) is made of petroleum as a raw material, but its thickness is suppressed to the minimum necessary for heat insulation. For this reason, the use of fossil fuels is reduced as much as possible, and the environmental load is small compared with a container made entirely of expanded polystyrene, and the printability is excellent.
However, since the moisture contained in the paper substrate is evaporated by heating and the thermoplastic resin layer is foamed by the evaporated moisture to provide heat insulation, if the moisture in the paper is low, foaming is not possible. If it becomes sufficient and does not foam sufficiently, high heat insulation cannot be obtained. And since paper with a low basis weight has a low water content and is inferior in foaming properties, a paper substrate with a high basis weight must be used.
On the other hand, the paper container is formed into a cup shape from the body member and the bottom plate member, and in particular, the upper edge of the opening of the container body member is an upper portion as in Patent Document 3 for giving mouthfeel and strength when eating and drinking. Although a flange portion is provided, when paper having a high basis weight is used, it is difficult to perform the molding process, and the entire cost is increased. Furthermore, if the container is lightweight, it is advantageous from the viewpoint of transportation and recycling, and it is desirable that the basis weight of the paper be low.
Therefore, an object of the present invention is to provide a paper container that has sufficient foaming properties and excellent heat insulation properties without increasing the basis weight of the paper.
(1) 断熱性紙製容器に用いる原材料シートにおいて、
紙基材の少なくとも片面に熱可塑性樹脂層を形成した原材料シートであって、
該紙基材の坪量が250g/m2以上かつ離解ろ水度がカナダ標準ろ水度で360ml以下であるととともに、
前記熱可塑性樹脂層が紙基材中に含有されている水分の加熱蒸発により発泡されるものであることを特徴とする原材料シート。
(2) 胴部材と底板部材とからなる断熱性紙製容器において、
胴部材及び/又は底板部材は紙基材の少なくとも片面に熱可塑性樹脂製発泡層を備えた紙製材料を用いた断熱性紙製容器であって、
前記紙基材の坪量が250g/m2以上かつ離解ろ水度がカナダ標準ろ水度で360ml以下であるととともに、
前記熱可塑性樹脂製発泡層が紙基材に含有されている水分を加熱蒸発させて発泡形成された層であることを特徴とする断熱性紙製容器。
(3)(1)又は(2)に記載された紙基材が、パルプとしてNBKPおよびLBKPを含有し、NBKP/LBKP比が30/70以下であることを特徴とする原材料シート又は断熱性紙製容器。
(4)紙基材は密度が0.91g/cm3以下、0.6g/cm3以上であることを特徴とする(1)〜(3)のいずれかに記載された原材料シート又は断熱性紙製容器。
(5)紙基材は、紙面PHが6以下であることを特徴とする(1)〜(4)のいずれかに記載された原材料シート又は断熱性紙製容器。
(6)紙基材がポリビニルアルコールまたは澱粉を含有し、かつその塗布量が2g/m2以下であることを特徴とする(1)〜(5)のいずれかに記載された原材料シート又は断熱性紙製容器。
(7)熱可塑性樹脂製発泡層は、層厚が1200μm以上であることを特徴とする(1)〜(6)のいずれかに記載された原材料シート又は断熱性紙製容器。
(8)熱可塑性樹脂製発泡層は、発泡処理前熱可塑性樹脂層を15〜25倍して形成されたものであることを特徴とする(1)〜(7)のいずれかに記載された原材料シート又は断熱性紙製容器。
(1) In the raw material sheet used for the insulating paper container,
A raw material sheet in which a thermoplastic resin layer is formed on at least one side of a paper substrate,
The basis weight of the paper substrate is 250 g / m 2 or more and the disaggregation freeness is a Canadian standard freeness of 360 ml or less,
A raw material sheet, wherein the thermoplastic resin layer is foamed by heating and evaporation of moisture contained in a paper substrate.
(2) In a heat insulating paper container composed of a trunk member and a bottom plate member,
The body member and / or the bottom plate member is a heat insulating paper container using a paper material provided with a thermoplastic resin foam layer on at least one side of a paper substrate,
The basis weight of the paper base material is 250 g / m 2 or more and the disaggregation freeness is a Canadian standard freeness of 360 ml or less,
2. A heat insulating paper container, wherein the thermoplastic resin foam layer is a foamed layer formed by heating and evaporating moisture contained in a paper base material.
(3) The raw material sheet or heat insulating paper, wherein the paper base material described in (1) or (2) contains NBKP and LBKP as pulp and has an NBKP / LBKP ratio of 30/70 or less. Made container.
(4) The paper substrate density of 0.91 g / cm 3 or less, and wherein the at 0.6 g / cm 3 or more (1) to (3) Raw materials sheet or thermal insulation according to any one of Paper container.
(5) The raw material sheet or heat insulating paper container described in any one of (1) to (4), wherein the paper base has a paper surface PH of 6 or less.
(6) The raw material sheet or heat insulation described in any one of (1) to (5), wherein the paper base material contains polyvinyl alcohol or starch, and the coating amount is 2 g / m 2 or less. Sex paper container.
(7) The foamed layer made of a thermoplastic resin has a layer thickness of 1200 μm or more, and is a raw material sheet or a heat insulating paper container described in any one of (1) to (6).
(8) The thermoplastic resin foam layer is formed by multiplying the thermoplastic resin layer before foaming by 15 to 25 times, and is described in any one of (1) to (7), Raw material sheet or insulated paper container.
・発泡性良好で十分な発泡層の厚さが得られ、断熱性に優れた紙製容器が提供できる。
・低坪量の紙を使用しても、高坪量の紙を使用した場合と同等の断熱効果を付与することができるため、省資源化およびコストダウンが可能である。
・発泡ポリスチレンを使用しない紙を主成分とする容器であり、環境に配慮した容器、人体への影響が少ない容器であって、紙系のゴミとして処理することができる。
-A foam container having good foamability and sufficient foam layer thickness can be obtained, and a paper container excellent in heat insulation can be provided.
・ Even if low-basis weight paper is used, the same heat insulation effect as when high-basis weight paper is used can be imparted, so that resource saving and cost reduction are possible.
A container mainly composed of paper that does not use expanded polystyrene, is an environmentally friendly container, and has little influence on the human body, and can be treated as paper-based waste.
以下、本発明の紙製容器について図面に基づき説明するが、本発明はこれらに限定されるものではない。
図1は、本発明による紙製容器の一例の断面図である。本発明の紙製容器1は、基本的に胴部材2と底板部材3とから構成されている。
図2は、図1においてYで示された胴部の部分拡大断面斜視図である。本例では、胴部材の外壁面側(容器外側)に、紙基材4の表面に熱可塑性樹脂製発泡層すなわち発泡した熱可塑性樹脂層5(以下、発泡熱可塑性樹脂層5という)が存在しており、発泡熱可塑性樹脂層5は、発泡セル6が並んだ構造となっている。胴部の内壁面側(容器内側)には、発泡熱可塑性樹脂層5の熱可塑性樹脂よりも融点の高い熱可塑性樹脂からなる熱可塑性樹脂層7(以下、非発泡熱可塑性樹脂層7という)が存在している。この非発泡熱可塑性樹脂層7は、後述するように、容器製造における加熱処理の際に発泡せず、紙基材からの蒸発水分の逃散を防止して発泡熱可塑性樹脂層5を確実かつ十分に発泡させるものである。
Hereinafter, although the paper container of this invention is demonstrated based on drawing, this invention is not limited to these.
FIG. 1 is a cross-sectional view of an example of a paper container according to the present invention. The paper container 1 of the present invention is basically composed of a body member 2 and a bottom plate member 3.
FIG. 2 is a partially enlarged cross-sectional perspective view of the body portion indicated by Y in FIG. In this example, a thermoplastic resin foam layer, that is, a foamed thermoplastic resin layer 5 (hereinafter referred to as a foamed thermoplastic resin layer 5) is present on the surface of the paper substrate 4 on the outer wall surface side (outside of the container) of the body member. The foamed thermoplastic resin layer 5 has a structure in which foamed cells 6 are arranged. A thermoplastic resin layer 7 made of a thermoplastic resin having a melting point higher than that of the thermoplastic resin of the foamed thermoplastic resin layer 5 (hereinafter referred to as a non-foamed thermoplastic resin layer 7) is provided on the inner wall surface side (inner side of the container) of the trunk portion. Is present. As will be described later, the non-foamed thermoplastic resin layer 7 does not foam during the heat treatment in the container production, prevents the escape of evaporated water from the paper base material, and makes the foamed thermoplastic resin layer 5 reliable and sufficient. It is made to foam.
[紙基材]
(紙)
本発明で使用される紙とは、植物繊維または植物繊維とその他の繊維とを絡み合わせ膠着させて製造したものをいい、製紙分野で公知の方法により製造される。植物繊維としては針葉樹または広葉樹などの木材繊維、ミツマタ、コウゾなどの靭皮繊維、バガス、ケナフ、麻などの非木材繊維、木綿繊維、古紙等が挙げられこれらに限定されるものではないが、地球環境問題を背景とした廃棄物処理や環境負荷の観点から、植物繊維100%の組成からなる紙が好ましい。
木材繊維のパルプとして、具体的には、針葉樹、広葉樹などを用いた化学パルプ;針葉樹の晒クラフトパルプ(NBKP)、未晒クラフトパルプ(NUKP)、広葉樹の晒クラフトパルプ(LBKP)、未晒クラフトパルプ(LUKP)等、機械パルプ;グラウンドウッドパルプ(GP)、リファイナーメカニカルパルプ(RGP)、サーモメカニカルパルプ(TMP)、ケミサーモメカニカルパルプ(CTMP)等、脱墨パルプ(DIP)等が挙げられ、これらを単独または任意の割合で混合して使用される。なお、脱墨パルプは再生パルプとも呼ばれる。本発明では、中でも、針葉樹の晒クラフトパルプ(以下NBKPという)または広葉樹の晒クラフトパルプ(以下LBKPという)は、含水率および汎用性の面から好適である。
[Paper base]
(paper)
The paper used in the present invention refers to a paper fiber or a paper fiber that is produced by intertwining vegetable fibers and other fibers and is produced by a method known in the papermaking field. Examples of plant fibers include, but are not limited to, wood fibers such as conifers or hardwoods, bast fibers such as Mitsumata and Kozo, non-wood fibers such as bagasse, kenaf and hemp, cotton fibers, and waste paper. From the viewpoint of waste disposal and environmental load against the background of global environmental problems, paper composed of 100% plant fiber is preferred.
Specific examples of wood fiber pulp include chemical pulp using conifers and hardwoods; bleached kraft pulp of conifers (NBKP), unbleached kraft pulp (NUKP), bleached kraft pulp of hardwood (LBKP), unbleached kraft Pulp (LUKP) and the like, mechanical pulp; groundwood pulp (GP), refiner mechanical pulp (RGP), thermomechanical pulp (TMP), chemithermomechanical pulp (CTMP), deinked pulp (DIP) and the like, These may be used alone or in admixture at any ratio. The deinked pulp is also called regenerated pulp. In the present invention, among them, softwood bleached kraft pulp (hereinafter referred to as NBKP) or hardwood bleached kraft pulp (hereinafter referred to as LBKP) is preferable in terms of moisture content and versatility.
紙の製造方法としては、一般的に、上記のパルプ、水、および必要に応じて填料やその他薬品等を添加して調成した紙料を抄紙機のワイヤー上に噴射し、ワイヤーパートで脱水、プレスパートで搾水、ドライヤーパートで乾燥、また必要に応じて紙に強度や耐水性を付与するサイズプレスや、紙の表面の凹凸を整えるカレンダーを施して抄紙し、仕上がった紙を巻取り所定の巻取寸法に仕上げて完成される。なお、本発明における紙の製造はこれに制限されるものではない。 As a method for producing paper, generally, the above pulp, water, and paper material prepared by adding fillers and other chemicals as needed are sprayed onto the wire of the paper machine, and dewatered at the wire part. Squeezed in the press part, dried in the dryer part, and if necessary, made paper by applying a size press that gives the paper strength and water resistance, and a calendar that adjusts the unevenness of the paper surface, and then winding the finished paper Finished to a predetermined winding dimension and completed. The production of paper in the present invention is not limited to this.
(坪量)
本発明では、紙中の加熱蒸発水分を利用して熱可塑性樹脂層が発泡する機構であることから、紙の坪量が重要であり、坪量は含有される水分の量に影響する。坪量が低すぎる場合は、発泡に必要な水分が少ないためか十分に発泡せず、また、容器を手で把持したときに熱さを感じやすい。坪量が高すぎる場合は、水分量が多くなって必要以上に発泡し過発泡や発泡セルの破裂などを招いたり、胴部材として所望の剛度を超えて不経済であり、また、容器の成型加工性が低下して上部フランジ部の形成も困難になる。
(Basis weight)
In the present invention, the basis weight of the paper is important because it is a mechanism in which the thermoplastic resin layer is foamed using the heat-evaporated moisture in the paper, and the basis weight affects the amount of moisture contained. When the basis weight is too low, foaming does not occur sufficiently because of the small amount of water necessary for foaming, and it is easy to feel heat when the container is held by hand. If the basis weight is too high, the amount of water increases and foams more than necessary, leading to over-foaming and rupture of the foamed cells, etc. The workability is lowered and it is difficult to form the upper flange portion.
本発明では、坪量が100g/m2以上、400g/m2以下が好適であり、好ましくは200g/m2以上、さらに好ましくは250g/m2以上、よりさらに好ましくは270g/m2以上である。紙中の含水率としては、5〜15重量%が好ましく、6〜10重量%であるとさらに好ましい。水分量は、20〜32g/m2程度が適当である。 In the present invention, the basis weight is preferably 100 g / m 2 or more and 400 g / m 2 or less, preferably 200 g / m 2 or more, more preferably 250 g / m 2 or more, and even more preferably 270 g / m 2 or more. is there. The water content in the paper is preferably 5 to 15% by weight, more preferably 6 to 10% by weight. An appropriate amount of water is about 20 to 32 g / m 2 .
(離解ろ水度)
本発明では、紙の離解ろ水度に着目し、離解ろ水度が360ml以下であるとき、紙の坪量を高くすることなく優れた発泡性を得ることができる、言い換えれば、発泡性を損なわずに坪量を低くすることができることを見出しなされたものである。離解ろ水度が360ml以下であるとき、優れた発泡性が得られる理由は明らかではないが、次のように考えられる。紙の製造において、パルプは叩いてほぐす(叩解)ことが行われるが、この叩解処理により、パルプ繊維からヒゲが出たり柔らかくなり、繊維同士の絡み合いや繊維間結合が促進されて紙の強度が高まる。叩解の度合いはろ水度で測定され、原理は網に一定量のパルプと水を混ぜたものをのせ、網目から落ちる水量を調べる。叩解が進んだものほど値は小さく、紙の強度が高くなるといえるが、しかし、繊維間の接着力は増すものの繊維自身の強さが減少しているため、引張り強さや引裂き強さなど低下させてしまう。これに対し、本発明では、離解ろ水度が360ml以下の紙であることにより、繊維細胞壁が内部の水分を放出しやすいように損傷されているため、格段に優れた発泡性が得られると考えられる。360mlを超えると、発泡が不十分で高い断熱性が得られない。より好ましくは344ml以下、さらに好ましくは320ml以下である。但し、離解ろ水度が低い紙の場合、密度が高くなって嵩が出ない、不透明度が低下する、繊維の損傷が激しく紙の強度が著しく低下するなどの弊害もあり、容器として必要な厚さや剛度が得られにくいため、離解ろ水度の下限は150ml以上であることが好ましい。
(Determination freeness)
In the present invention, paying attention to the degree of freezing and freezing of paper, when the degree of freezing and freezing is 360 ml or less, excellent foamability can be obtained without increasing the basis weight of the paper. It has been found that the basis weight can be lowered without damage. The reason why excellent foamability can be obtained when the disaggregation freeness is 360 ml or less is not clear, but is considered as follows. In the manufacture of paper, pulp is beaten and loosened (beating), but this beating process causes whiskers to come out and soften from the pulp fibers, entanglement of fibers and interfiber bonding are promoted, and the strength of the paper is increased. Rise. The degree of beating is measured by freeness, and the principle is to put a certain amount of pulp and water on a net and check the amount of water falling from the net. The more advanced the beating, the smaller the value and the higher the strength of the paper, but the strength of the fiber itself is reduced, although the adhesion between the fibers increases, but the tensile strength and tear strength are reduced. End up. On the other hand, in the present invention, since the disintegration freezing degree is paper of 360 ml or less, the fiber cell wall is damaged so as to easily release the internal moisture, and thus a significantly excellent foaming property is obtained. Conceivable. When it exceeds 360 ml, foaming is insufficient and high heat insulation cannot be obtained. More preferably, it is 344 ml or less, More preferably, it is 320 ml or less. However, in the case of paper with low disaggregation freeness, there is a problem such as high density and no bulk, opacity decreases, fiber damage is severe and paper strength is remarkably reduced, and it is necessary as a container. Since it is difficult to obtain thickness and rigidity, the lower limit of the disaggregation freeness is preferably 150 ml or more.
なお、本発明における離解ろ水度は、紙を水に再離解したときのJIS−P−8121に基づくカナダ標準ろ水度(以下、CSFということがある)で表される。離解ろ水度の測定は、紙製容器の発泡した胴部材を数日間水に浸漬して熱可塑性樹脂層を剥離・除去した後、所定の大きさにして水に浸漬した状態でさらに一昼夜放置後、結束繊維がみられない程度まで離解し、冷却してJIS−P−8121に準じて行う。
また、パルプ段階でのろ水度としては、CSFが約470ml以下であると、離解ろ水度が360ml以下の紙が得られやすく好ましい。下限としては200ml以上である。パルプのCSFが低すぎると、抄紙時に脱水性が悪化する、締まった紙になり低密度で嵩のある紙が得られない、不透明度の高い紙が得られない、引裂強度の高い紙が得られないなどの問題がある。また、本発明では異なる種類のパルプを併用してもよく、その場合のCSFは、それぞれのパルプではなく混合したものが470ml以下となるようにする。パルプを併用する場合、NBKPとLBKPとを用いることが好ましく、NBKPの割合が全パルプ重量に対し50重量%未満、さらには30重量%以下であることが好ましい。通常、NBKPはCSFを高目にする傾向があり、NBKPの配合割合が多くなると発泡性が低下しやすい。NBKPは引裂強度を高めるために混ぜているため、あまり叩かないことが好ましい。
The disaggregation freeness in the present invention is represented by the Canadian standard freeness (hereinafter sometimes referred to as CSF) based on JIS-P-8121 when paper is disaggregated again in water. For the measurement of the degree of water removal, the foamed body of the paper container is immersed in water for several days to remove and remove the thermoplastic resin layer, and then left to stand for a whole day and night in a predetermined size soaked in water. Then, it disaggregates to such an extent that a binding fiber is not seen, it cools, and it carries out according to JIS-P-8121.
Further, the freeness at the pulp stage is preferably about 470 ml or less because the paper having a disaggregation freeness of 360 ml or less is easily obtained. The lower limit is 200 ml or more. If the CSF of the pulp is too low, the dewaterability will deteriorate during paper making, it will become a tight paper, a paper with low density and bulk will not be obtained, a paper with high opacity will not be obtained, and a paper with high tear strength will be obtained There are problems such as inability. Further, in the present invention, different types of pulp may be used in combination, and the CSF in that case is not pulverized but mixed to be 470 ml or less. When using a pulp together, it is preferable to use NBKP and LBKP, and it is preferable that the ratio of NBKP is less than 50 weight% with respect to the total pulp weight, Furthermore, it is preferable that it is 30 weight% or less. Normally, NBKP tends to increase the CSF, and the foaming property tends to decrease when the blending ratio of NBKP increases. Since NBKP is mixed in order to increase the tear strength, it is preferable that the NBKP is not hit too much.
(密度)
本発明では密度が低い方が、蒸発水分が通りやすく発泡性が良好になると考えられ好ましい。但し、低すぎると容器に必要な紙力が得られず、また後述する熱可塑性樹脂層のラミネート適性に劣り、高すぎると容器として必要な厚さが得られないため、0.91g/cm3以下、0.6g/cm3以上が好適である。ただし、紙の密度は所望に応じて適宜設定すればよく特にこの範囲に限定されない。
(density)
In the present invention, it is preferable that the density is low because it is considered that evaporative moisture easily passes and foamability is improved. However, if it is too low, the paper strength required for the container cannot be obtained, and the thermoplastic resin layer, which will be described later, is inferior in laminating properties. If it is too high, the necessary thickness for the container cannot be obtained, so 0.91 g / cm 3 Hereinafter, 0.6 g / cm 3 or more is preferable. However, the density of the paper may be appropriately set as desired, and is not particularly limited to this range.
(紙面PH)
紙面PHとしては6以下となることが望ましい。紙面PHがアルカリ性側では繊維が水を保持しやすい状態になるのに対し、酸性側では水分を放出しやすく発泡性が良好となると考えられる。ただし、特にこれに限定されるのではなく紙の種類は、抄紙PHが酸性領域で抄紙される酸性紙、抄紙PHが疑似中性領域で抄紙される疑似中性紙、抄紙PHが中性領域で抄紙される中性紙、抄紙PHがアルカリ性領域で抄紙されるアルカリ性紙のいずれでもよく、また、酸性領域で抄紙された酸性原紙の表面にアルカリ性薬剤を塗布した中性紙も可能である。
(Paper PH)
The paper surface PH is desirably 6 or less. On the alkaline side of the paper PH, the fibers are likely to retain water, whereas on the acidic side, moisture is likely to be released and foamability is considered to be good. However, the type of paper is not limited to this, and the types of paper are acidic paper in which papermaking PH is made in an acidic region, pseudo-neutral paper in which papermaking PH is made in a pseudo-neutral region, and papermaking PH is in a neutral region. Neutral papers made in step (1) and alkaline papers made from paper PH in the alkaline region may be used, and neutral papers coated with an alkaline agent on the surface of the acidic base paper made in the acidic region are also possible.
(填料、その他薬品等)
本発明で用いられる紙は、填料は無配合でも配合してもよく、発泡性へ影響するため無配合が望ましいが、不透明度を高める観点からは配合してもよい。填料を配合する場合、種類は製紙分野で一般に使用されている填料が使用でき、特に限定されるものではない。例えば、クレー、焼成カオリン、デラミカオリン、重質炭酸カルシウム、軽質炭酸カルシウム、軽質炭酸カルシウム−シリカ複合物、炭酸マグネシウム、炭酸バリウム、二酸化チタン、酸化亜鉛、酸化珪素、非晶質シリカ、水酸化アルミニウム、水酸化カルシウム、水酸化マグネシウム、水酸化亜鉛などの無機填料、尿素−ホルマリン樹脂、ポリスチレン樹脂、フェノール樹脂、微小中空粒子等の有機填料が単独でまたは適宜2種類以上を組み合わせて使用される。また酸性抄紙では、前記中性抄紙で使用する填料から、酸溶解性のものを除いた填料が使用され、その単独または適宜2種類以上を組み合わせて使用される。
また、各種の内添サイズ剤を配合してもよく、従来から使用されている各種のノニオン性、カチオン性あるいは両性の歩留まり向上剤、濾水度向上剤、紙力向上剤等の製紙用内添助剤が必要に応じて適宜選択して使用される。さらに、例えば、硫酸バンド、塩化アルミニウム、アルミン酸ソーダや、塩基性塩化アルミニウム、塩基性ポリ水酸化アルミニウム等の塩基性アルミニウム化合物や、水に易分解性のアルミナゾル等の水溶性アルミニウム化合物、硫酸第一鉄、硫酸第二鉄等の多価金属化合物、シリカゾル等が内添されてもよい。
(Fillers, other chemicals, etc.)
In the paper used in the present invention, the filler may be blended without blending, and blending is desirable because it affects foaming properties, but it may be blended from the viewpoint of increasing opacity. When the filler is blended, the filler generally used in the papermaking field can be used and is not particularly limited. For example, clay, calcined kaolin, deramikaolin, heavy calcium carbonate, light calcium carbonate, light calcium carbonate-silica composite, magnesium carbonate, barium carbonate, titanium dioxide, zinc oxide, silicon oxide, amorphous silica, aluminum hydroxide Inorganic fillers such as calcium hydroxide, magnesium hydroxide, and zinc hydroxide, and organic fillers such as urea-formalin resin, polystyrene resin, phenol resin, and fine hollow particles may be used alone or in appropriate combination of two or more. Further, in acidic papermaking, a filler obtained by removing acid-soluble ones from the filler used in the neutral papermaking is used, and these are used alone or in combination of two or more as appropriate.
Various internal sizing agents may be blended, and various types of conventionally used nonionic, cationic or amphoteric yield improvers, freeness improvers, paper strength improvers, etc. An auxiliary agent is appropriately selected and used as necessary. Further, for example, basic aluminum compounds such as sulfuric acid band, aluminum chloride, sodium aluminate, basic aluminum chloride and basic polyaluminum hydroxide, water-soluble aluminum compounds such as water-degradable alumina sol, sulfuric acid A polyvalent metal compound such as ferrous sulfate or ferric sulfate, silica sol, or the like may be internally added.
その他、製紙用助剤として各種澱粉類、ポリアクリルアミド、尿素樹脂、メラミン樹脂、エポキシ樹脂、ポリアミド樹脂、ポリアミド、ポリアミン樹脂、ポリアミン、ポリエチレンイミン、植物ガム、ポリビニルアルコール、ラテックス、ポリエチレンオキサイド、親水性架橋ポリマー粒子分散物及びこれらの誘導体あるいは変性物等の各種化合物を使用できる。
さらに、染料、蛍光増白剤、PH調整剤、消泡剤、ピッチコントロール剤、スライムコントロール剤等の抄紙用内添剤を用途に応じて適宜添加することもできる。
Other papermaking aids such as various starches, polyacrylamide, urea resin, melamine resin, epoxy resin, polyamide resin, polyamide, polyamine resin, polyamine, polyethyleneimine, vegetable gum, polyvinyl alcohol, latex, polyethylene oxide, hydrophilic crosslinking Various compounds such as polymer particle dispersion and derivatives or modified products thereof can be used.
Furthermore, internal additives for papermaking such as dyes, fluorescent brighteners, pH adjusters, antifoaming agents, pitch control agents, slime control agents, and the like can be appropriately added depending on the application.
(抄紙)
抄紙機の型式は特に限定は無く、長網抄紙機、ツインワイヤー抄紙機、円網式抄紙機、ギャップフォーマー、ハイブリッドフォーマー(オントップフォーマー)等の公用の抄紙機で抄紙することができる。プレス線圧は通常の操業範囲内で用いられる。また、平滑性を付与し印刷適性を向上させる目的などから、カレンダー処理を行ってもよい。カレンダーは通常の操業範囲内の線圧で用いられるが、本発明では水分の蒸発しやすさ紙が嵩高である方がより望ましく、その場合には、紙の平滑性を維持できる範囲でなるべく低線圧またはバイパスが好ましい。また、通常のカレンダーよりもソフトカレンダーが好ましい。
本発明で用いられる紙は、全く塗工処理をしていないか、あるいは顔料を含まない表面処理剤を塗工してもよい。また、表面強度やサイズ性の向上の目的で、水溶性高分子を主成分とする表面処理剤を塗工してもよい。水溶性高分子としては、澱粉、酸化澱粉、加工澱粉、カルボキシメチルセルロース、ポリアクリルアミド、ポリビニルアルコール等の表面処理剤として通常使用されるものを単独、あるいはこれらの混合物を使用することができる。また、表面処理剤の中には、水溶性高分子の他に耐水化、表面強度向上を目的とした紙力増強剤やサイズ性付与を目的とした外添サイズ剤を添加することができる。表面処理剤の塗布方法としては、表面処理剤は、2ロールサイズプレスコーター、ゲートロールコーター、ブレードメタリングコーター、ロッドメタリングコーター等の塗工機によって塗布することができるが、ゲートロールコーターのような被膜転写方式の塗工機を使用する方が表面処理剤が紙表面に留まり、密度の増加が少なくなるので好ましい。表面処理剤の塗布量としては、片面当たり0.1g/m2以上、3g/m2以下程度である。
(Paper making)
There are no particular restrictions on the type of paper machine, and paper machines can be used on public paper machines such as long paper machines, twin-wire paper machines, circular net paper machines, gap formers, and hybrid formers (on-top formers). it can. The press line pressure is used within the normal operating range. Further, for the purpose of imparting smoothness and improving printability, a calendar process may be performed. The calender is used at a linear pressure within the normal operating range. However, in the present invention, it is more desirable that the paper is easy to evaporate moisture, and the paper is more bulky. In that case, it is as low as possible within the range where the smoothness of the paper can be maintained. Linear pressure or bypass is preferred. A soft calendar is preferable to a normal calendar.
The paper used in the present invention may not be coated at all or may be coated with a surface treatment agent containing no pigment. Moreover, you may apply the surface treating agent which has a water-soluble polymer as a main component in order to improve surface strength or size property. As the water-soluble polymer, those usually used as a surface treating agent such as starch, oxidized starch, processed starch, carboxymethyl cellulose, polyacrylamide, polyvinyl alcohol, etc. can be used alone or a mixture thereof. In addition to the water-soluble polymer, a paper strength enhancer for the purpose of water resistance and surface strength improvement and an external sizing agent for the purpose of imparting sizing can be added to the surface treatment agent. As a method for applying the surface treatment agent, the surface treatment agent can be applied by a coating machine such as a two-roll size press coater, a gate roll coater, a blade metalling coater, or a rod metalling coater. It is preferable to use such a coat transfer type coating machine because the surface treatment agent remains on the paper surface and the increase in density is reduced. The coating amount of the surface treatment agent is about 0.1 g / m 2 or more and 3 g / m 2 or less per side.
(サイズプレス)
また、本発明においては、前記のカレンダー処理時にポリビニルアルコール、澱粉等の表面処理剤や外添サイズ剤等を塗工することも好ましい。このような方法はサイズプレスと呼ばれ、2ロールサイズプレス、フィルムトランスファーサイズプレス、カレンダーサイジング等がある。サイズプレスの後、通常のカレンダー処理を行っても良い。サイズプレスによる表面処理剤の塗布は、表面強度の向上や紙粉の発生の防止効果が高い。さらに、通常、製紙の乾燥工程では抄紙機の幅方向中央になるほど乾きにくく、均一な水分プロファイルが得られにくいところ、サイズプレスによって水分を幅方向で揃えることができ、水分プロファイルが均一になることにより、加熱蒸発にムラがなく均質な発泡熱可塑性樹脂層を得ることができる。なお、表面処理剤を含まず水を用いてもよいが、ポリビニルアルコール、澱粉等は適度な粘度を持つため水に比べて広がりやすく、水分均一化の効果が大きくなるため好ましい。この場合のポリビニルアルコール、澱粉等の塗布量としては、多すぎても水分蒸発が妨げられる傾向があるため、2g/m2以下、より好ましくは0.9g/m2以下、さらに好ましくは0.5g/m2以下である。
(Size press)
In the present invention, it is also preferable to coat a surface treatment agent such as polyvinyl alcohol or starch, an external sizing agent, or the like during the calendar treatment. Such a method is called a size press and includes a two-roll size press, a film transfer size press, a calendar sizing, and the like. A normal calendar process may be performed after the size press. The application of the surface treatment agent by the size press is highly effective in improving the surface strength and preventing the generation of paper dust. In addition, it is usually difficult to dry the paper machine in the drying process in the center of the paper machine in the width direction, and it is difficult to obtain a uniform moisture profile. As a result, it is possible to obtain a uniform foamed thermoplastic resin layer without unevenness in heating and evaporation. Although water may be used without containing a surface treatment agent, polyvinyl alcohol, starch, and the like are preferable because they have an appropriate viscosity and thus are easier to spread than water, and the effect of water uniformity is increased. In this case, the coating amount of polyvinyl alcohol, starch and the like tends to hinder the evaporation of water even if it is too much, so that it is 2 g / m 2 or less, more preferably 0.9 g / m 2 or less, still more preferably 0.8. 5 g / m 2 or less.
[発泡熱可塑性樹脂層]
本発明の紙製容器の胴部材原材料シートは、上記の紙基材上に、紙に含有されている水分の加熱蒸発により発泡する熱可塑性樹脂層を積層して作製される。
発泡熱可塑性樹脂層となる熱可塑性樹脂としては、押出しラミネートが可能でかつ発泡可能であれば特に制限されず、結晶性樹脂、非結晶性樹脂のどちらの熱可塑性樹脂も使用することができる。結晶性樹脂としてはポリエチレン、ポリプロピレン、ポリメチルペンテン等のポリオレフィン系樹脂や、ポリエステル系樹脂、ポリアミド、ポリアセタール、PPS樹脂等を挙げることができる。非結晶性樹脂としては、ポリスチレン、ポリ塩化ビニル、ABS樹脂、アクリル樹脂、変性PPE、ポリカーボネート、ポリウレタン、ポリ酢酸ビニル、非結晶性ポリエチレンテレフタレート(PET)等を挙げることができる。これらの熱可塑性樹脂の融点としては、80〜120℃程度が好ましい。また、これらの熱可塑性樹脂は単一の樹脂を単層で使用しても、複数の樹脂を複層で使用しても良いが、発泡性の点から単層であることが好ましい。
[Foamed thermoplastic resin layer]
The body member raw material sheet of the paper container of the present invention is produced by laminating a thermoplastic resin layer foamed by heating and evaporation of moisture contained in the paper on the paper base material.
The thermoplastic resin used as the foamed thermoplastic resin layer is not particularly limited as long as extrusion lamination is possible and foaming is possible, and either a crystalline resin or an amorphous resin can be used. Examples of the crystalline resin include polyolefin resins such as polyethylene, polypropylene, and polymethylpentene, polyester resins, polyamide, polyacetal, and PPS resins. Examples of the amorphous resin include polystyrene, polyvinyl chloride, ABS resin, acrylic resin, modified PPE, polycarbonate, polyurethane, polyvinyl acetate, and amorphous polyethylene terephthalate (PET). The melting point of these thermoplastic resins is preferably about 80 to 120 ° C. These thermoplastic resins may be a single resin or a plurality of resins, but are preferably a single layer from the viewpoint of foamability.
さらに、本発明では、ラミネート適性、発泡性に優れることからポリエチレンが好ましい。ポリエチレンは、大きくは直鎖状低密度ポリエチレン、低密度ポリエチレン、中密度ポリエチレン、高密度ポリエチレンに区分される。密度としては、直鎖状低密度ポリエチレンは888〜910kg/m3、低密度ポリエチレンは910〜925kg/m3、中密度ポリエチレンは925〜940kg/m3、さらに高密度ポリエチレンは940〜970kg/m3程度である。融点としては、直鎖状低密度ポリエチレンは55℃〜120℃、低密度ポリエチレンは105〜120℃、中密度ポリエチレンは120〜125℃、さらに高密度ポリエチレンは125〜135℃程度である。 Furthermore, in the present invention, polyethylene is preferred because of excellent laminating ability and foamability. Polyethylene is roughly classified into linear low density polyethylene, low density polyethylene, medium density polyethylene, and high density polyethylene. The density, linear low density polyethylene 888~910kg / m 3, low density polyethylene 910~925kg / m 3, medium density polyethylene 925~940kg / m 3, higher density polyethylene has 940~970kg / m About three . As the melting point, linear low density polyethylene is 55 ° C to 120 ° C, low density polyethylene is 105 ° C to 120 ° C, medium density polyethylene is 120 ° C to 125 ° C, and high density polyethylene is about 125 ° C to 135 ° C.
[非発泡熱可塑性樹脂層]
本発明では、発泡効率を高めるために、胴部材の発泡熱可塑性樹脂層を有する壁面の反対壁面側を、発泡熱可塑性樹脂層よりも融点の高い熱可塑性樹脂からなるとともに加熱処理した際に発泡しない熱可塑性樹脂層(非発泡熱可塑性樹脂層)、あるいはアルミ箔等で被覆することが好ましい。紙基材の片面が地のままだと、加熱処理の際にこの未被覆面から紙中の水分が大気中に蒸散してしまい、十分確実に発泡させることが難しくなる。従って、このような被覆層を設けることにより、紙中の水分を効率良く発泡に寄与させることができる。なお、これらの非発泡熱可塑性樹脂層やアルミ箔などは、胴部材の内壁面側に存在すると、充填液体等が紙中へ浸透することを防止でき好ましい。
同様に、発泡効率を高める目的で、発泡熱可塑性樹脂層の上に、非発泡熱可塑性樹脂層を設けることもできる。発泡熱可塑性樹脂層が胴部材の外壁面側に存在するときは、その表面は凹凸があり平滑ではないため、非発泡熱可塑性樹脂層の存在により、滑らかな手触りと光沢のある外観を得ることができ、容器の防水性もより向上する。
[Non-foamed thermoplastic resin layer]
In the present invention, in order to increase the foaming efficiency, the opposite wall surface side of the wall surface having the foamed thermoplastic resin layer of the body member is made of a thermoplastic resin having a melting point higher than that of the foamed thermoplastic resin layer and foamed when heat-treated. It is preferable to cover with an unheated thermoplastic resin layer (non-foamed thermoplastic resin layer) or an aluminum foil. If one side of the paper base is left ground, the moisture in the paper will evaporate from the uncoated surface into the atmosphere during the heat treatment, making it difficult to ensure sufficient foaming. Therefore, by providing such a coating layer, moisture in the paper can be efficiently contributed to foaming. It should be noted that these non-foamed thermoplastic resin layers, aluminum foils, and the like are preferably present on the inner wall surface side of the body member, so that the filling liquid or the like can be prevented from penetrating into the paper.
Similarly, a non-foamed thermoplastic resin layer can be provided on the foamed thermoplastic resin layer for the purpose of increasing the foaming efficiency. When the foamed thermoplastic resin layer is present on the outer wall surface of the body member, the surface is uneven and not smooth, so that the presence of the non-foamed thermoplastic resin layer provides a smooth hand and glossy appearance. And the waterproofness of the container is further improved.
これらの非発泡熱可塑性樹脂層の熱可塑性樹脂は、発泡熱可塑性樹脂層と同一であっても異なっていてもよい。同一の場合は、密度に差を持たせることにより融点に差を生じさせることができる。例えば、両者の熱可塑性樹脂としてポリエチレンを選択する場合、発泡熱可塑性樹脂層は低密度ポリエチレンとし、非発泡熱可塑性樹脂層は中密度または高密度ポリエチレンとする。発泡熱可塑性樹脂層と非発泡熱可塑性樹脂層の熱可塑性樹脂における融点の差は5℃以上あることが好ましく、非発泡熱可塑性樹脂層の熱可塑性樹脂の融点としては、加熱の際に融解せず蒸発水分の拡散を防止できればよく特に制限されないが、125℃以上が好ましい。 The thermoplastic resin of these non-foamed thermoplastic resin layers may be the same as or different from the foamed thermoplastic resin layer. In the case of the same, a difference in the melting point can be caused by making a difference in density. For example, when polyethylene is selected as both thermoplastic resins, the foamed thermoplastic resin layer is low density polyethylene and the non-foamed thermoplastic resin layer is medium density or high density polyethylene. The difference between the melting points of the thermoplastic resin of the foamed thermoplastic resin layer and the non-foamed thermoplastic resin layer is preferably 5 ° C. or more. The melting point of the thermoplastic resin of the non-foamed thermoplastic resin layer is the melting point during heating. There is no particular limitation as long as it can prevent the diffusion of evaporated water, but 125 ° C. or higher is preferable.
[熱可塑性樹脂層の積層方法]
発泡熱可塑性樹脂層および非発泡熱可塑性樹脂層の形成方法は特に制限されず、紙基材上に、押出しラミネート法の他、ウェットラミネート法、ドライラミネート法等の予めフィルム状にしたものと貼合する方法を適宜使用して積層すればよいが、紙基材との密着性、発泡性等の点から、押出しラミネート法が好ましい。押出しラミネートは、例えば、巻取から繰り出された紙基材の一表面に、Tダイから熱可塑性樹脂層を溶融樹脂膜の状態で押出し、クーリングロールとこれに対向するニップロールとの間で冷却しつつ圧着する方法である。押出しラミネートにおいて、樹脂の溶融温度、積層速度などの操業条件は、用いる樹脂の種類や装置によって適宜設定すればよく特に制限されないが、一般に、例えば溶融温度は200〜350℃程度、積層速度は50〜200m/分程度である。また、ニップロールとしては硬度70度以上(JIS K−6253)のものを用い、線圧は15kgf/cm以上で押圧・圧着を行うことが好ましい。
また、発泡熱可塑性樹脂層上に非発泡熱可塑性樹脂層を設ける場合や、発泡熱可塑性樹脂層を複数の熱可塑性樹脂層で形成する場合など、2以上の熱可塑性樹脂層を積層するときは、熱可塑性樹脂層間の密着性や生産効率の点から、複数台の押出機を用いて各熱可塑性樹脂を溶融状態でそれぞれのTダイに導き、各Tダイから同時に押出して積層接着する方法が適している。このような多層の熱可塑性樹脂層を同時に形成可能な方法は、押出しラミネート法の中で特に共押出しラミネート法と呼ばれる。さらに、熱可塑性樹脂層同士の間に接着性樹脂層を挟んで、樹脂層間の接着性を高めてもよい。なお、いずれの場合でも、必要に応じて紙基材や熱可塑性樹脂の接着性を向上させるために、コロナ処理、オゾン処理等を行ってもよい。
[Lamination method of thermoplastic resin layer]
The method for forming the foamed thermoplastic resin layer and the non-foamed thermoplastic resin layer is not particularly limited, and it is pasted on a paper substrate with a film-like material such as a wet laminate method or a dry laminate method in addition to an extrusion laminate method. The lamination method may be appropriately used for lamination, but the extrusion laminating method is preferable from the viewpoints of adhesion to a paper base material, foamability and the like. For example, extrusion lamination is performed by extruding a thermoplastic resin layer from a T-die in the form of a molten resin film onto one surface of a paper substrate that has been unwound from winding, and cooling between a cooling roll and a nip roll facing it. It is a method of crimping while. In extrusion lamination, the operating conditions such as the melting temperature of the resin and the laminating speed may be appropriately set depending on the type of resin used and the apparatus, but generally the melting temperature is about 200 to 350 ° C. and the laminating speed is 50, for example. It is about ~ 200 m / min. Further, it is preferable to use a nip roll having a hardness of 70 degrees or more (JIS K-6253) and pressing and pressure bonding with a linear pressure of 15 kgf / cm or more.
When laminating two or more thermoplastic resin layers, such as when a non-foamed thermoplastic resin layer is provided on the foamed thermoplastic resin layer, or when the foamed thermoplastic resin layer is formed of a plurality of thermoplastic resin layers, etc. From the viewpoint of adhesion between thermoplastic resin layers and production efficiency, there is a method in which each thermoplastic resin is led to each T die in a molten state using a plurality of extruders, and is extruded from each T die at the same time and laminated and adhered. Is suitable. Such a method capable of simultaneously forming a multilayer thermoplastic resin layer is called a coextrusion laminating method among the extrusion laminating methods. Further, an adhesive resin layer may be sandwiched between the thermoplastic resin layers to improve the adhesion between the resin layers. In any case, corona treatment, ozone treatment, or the like may be performed in order to improve the adhesion of the paper base material or the thermoplastic resin as necessary.
また、発泡熱可塑性樹脂層および非発泡熱可塑性樹脂層の各熱可塑性樹脂層の厚さについて、発泡熱可塑性樹脂層は、発泡させたときに所望の断熱性を付与するのに十分な厚さであればよく特に限定されないが、発泡前の厚さとして40〜80μm程度、発泡後は例えば70μm厚の発泡前の熱可塑性樹脂層の場合に、1200μm〜2000μm程度である。本発明では、70μm厚の発泡前の熱可塑性樹脂層を、1200〜1600μm厚の発泡層を形成することを実現した。従来技術では20μmの層厚等の薄い層を10倍程度に発泡させた例は開示されているが、その程度では断熱性が十分でないが、熱可塑性樹脂層が厚くなると発泡コントロールも困難となるので、従来の公知例では1000μmの発泡層も実現されてはいない。
また、非発泡熱可塑性樹脂層も、蒸発水分の飛散を防止するのに十分な厚さであって、胴部材の内壁面側に存在する場合は耐液体浸透性を確保きる厚さであれば特に限定されず、20〜50μm程度である。
Further, regarding the thickness of each of the thermoplastic resin layers of the foamed thermoplastic resin layer and the non-foamed thermoplastic resin layer, the foamed thermoplastic resin layer has a thickness sufficient to impart desired heat insulation properties when foamed. However, the thickness before foaming is about 40 to 80 μm, and after foaming, for example, in the case of the thermoplastic resin layer before foaming having a thickness of 70 μm, it is about 1200 μm to 2000 μm. In the present invention, a foamed layer having a thickness of 1200 to 1600 μm is formed from a thermoplastic resin layer having a thickness of 70 μm before foaming. In the prior art, an example in which a thin layer such as a 20 μm layer is foamed about 10 times is disclosed, but the thermal insulation is not sufficient at that level, but if the thermoplastic resin layer becomes thick, foam control becomes difficult. Therefore, a 1000 μm foam layer is not realized in the conventional known example.
Further, the non-foamed thermoplastic resin layer is also thick enough to prevent scattering of evaporated water, and if it is on the inner wall surface side of the body member, the thickness can ensure liquid penetration resistance. It is not specifically limited, It is about 20-50 micrometers.
また、容器の胴部材や底部材の外壁面側および内壁面側は、同じ積層構成であってもよいし異なっていてもよい。使用される樹脂の種類やその他の素材も、同一であってもよいし異なっていてもよい。
また、発泡熱可塑性樹脂層および非発泡熱可塑性樹脂層の各熱可塑性樹脂層には、所望の効果を阻害しない範囲で一般的に使用される種々の添加剤を添加することができる。これらの添加剤としては、例えば、帯電防止剤、白色顔料(酸化チタン、炭酸カルシウム、クレー、タルク、シリカ等の無機顔料等)、耐ブロッキング剤(アクリルビーズ、ガラスビーズ、シリカ等)、紫外線吸収剤などがある。
Further, the outer wall surface side and the inner wall surface side of the body member and the bottom member of the container may have the same laminated structure or may be different. The type of resin used and other materials may be the same or different.
In addition, various commonly used additives can be added to the thermoplastic resin layers of the foamed thermoplastic resin layer and the non-foamed thermoplastic resin layer as long as the desired effects are not impaired. Examples of these additives include antistatic agents, white pigments (inorganic pigments such as titanium oxide, calcium carbonate, clay, talc, and silica), anti-blocking agents (acrylic beads, glass beads, silica, etc.), and ultraviolet absorption. There are agents.
[紙製容器の成型]
本発明では、上記の胴部材原材料シートと底板部材原料シートとを常用のカップ製造装置やカップ成型機により成型する。まず、巻き取りロールから胴部材原材料シートを繰り出し、所定箇所に必要な印刷を施す。この段階でバーコードなどを印刷することもできる。印刷部分の位置決めなどは常用の手段または手順により行うことができる。
[Molding paper containers]
In the present invention, the body member raw material sheet and the bottom plate member raw material sheet are molded by a conventional cup manufacturing apparatus or cup molding machine. First, the body member raw material sheet is fed out from the take-up roll, and necessary printing is performed at a predetermined location. At this stage, barcodes can be printed. The positioning of the printed part can be performed by conventional means or procedures.
次に、それぞれの原材料シートから胴部材用ブランクと底板部材用ブランクを打ち抜き、常用のカップ成型機で容器の形に組み立てる。ここで、発泡熱可塑性樹脂層は、胴部材の外壁面側および内壁面側のどちらか片方あるいは両方に存在すればよく、断熱性、手触り、外観審美性など所望に応じて適宜決定すればよいが、容器内部を発泡面とした場合、飲食の際に発泡樹脂が箸やフォーク等により傷付いて口の中に入り込むおそれがあるため、外壁面側になるように存在することが望ましい。そこで、例えば、胴部材原材料シートの熱可塑性樹脂層が容器外側に向くように、また、底板部材は熱可塑性樹脂層面が容器内側に向くようにして、組み立てる。なお、底板部材原材料シートは、紙基材の少なくとも片面に1以上の熱可塑性樹脂層やアルミ泊等を設けたものが好ましく使用される。これは紙中への液体等の浸透防止のためである。底板部材に用いられる熱可塑性樹脂は、胴部材と同じであっても異なっていてもよく、積層方法も押出しラミネート法の他、ウェットラミネート法、ドライラミネート法等の予めフィルム状にしたものと貼合する方法が適宜使用できる。
カップ麺など湯を注入後しばらく放置するものは、容器底面からの放熱を防止する上で底部材にも発泡層を設けることが有効である。特に、屋外での用途や冬場や寒冷地では好ましい。また、蓋材も同様に発泡層を有するものを使用してもよい。
Next, a blank for a trunk member and a blank for a bottom plate member are punched out from each raw material sheet, and assembled into a container shape by a conventional cup molding machine. Here, the foamed thermoplastic resin layer only needs to be present on one or both of the outer wall surface side and the inner wall surface side of the body member, and may be appropriately determined as desired, such as heat insulation, touch, and appearance aesthetics. However, when the inside of the container is a foamed surface, the foamed resin may be damaged by chopsticks, forks or the like during food and drink and enter the mouth, so it is desirable that the container be on the outer wall surface side. Therefore, for example, the body member raw material sheet is assembled so that the thermoplastic resin layer faces the outside of the container, and the bottom plate member is assembled so that the surface of the thermoplastic resin layer faces the inside of the container. In addition, the bottom plate member raw material sheet is preferably used in which one or more thermoplastic resin layers, aluminum stays or the like are provided on at least one side of the paper base material. This is to prevent penetration of liquid or the like into the paper. The thermoplastic resin used for the bottom plate member may be the same as or different from that of the body member, and the lamination method is not only the extrusion lamination method but also a pre-film-like one such as a wet lamination method or a dry lamination method. The method to combine can be used suitably.
In order to prevent heat dissipation from the bottom of the container, it is effective to provide a foam layer on the bottom member of the cup noodles that are allowed to stand for a while after pouring hot water. In particular, it is preferable for outdoor use, winter and cold regions. Moreover, you may use the thing which has a foamed layer similarly.
[加熱処理による発泡]
成型後の紙製容器は、発泡させるために加熱処理を行う。本発明では、加熱処理により、胴部材の紙基材中に含まれる水分が蒸発して、熱可塑性樹脂層が発泡し発泡熱可塑性樹脂層となる。
加熱温度および熱時間は使用する紙基材および熱可塑性樹脂の種類に応じて変化し、使用する熱可塑性樹脂に対する最適な加熱温度と加熱時間の組み合わせは適宜決定することができるが、加熱温度は発泡する熱可塑性樹脂の融点よりもやや高い温度(融点+5〜10℃の範囲)が適し、一般的に、加熱温度約110℃〜約200℃程度、加熱時間約1分間〜約6分間程度である。加熱手段は特に限定されず、熱風、電熱、電子線など任意の手段を使用できる。コンベヤによる搬送手段を備えたトンネル内で、熱風または電熱などによって加熱すれば、安価に大量生産することができる。
[Foaming by heat treatment]
The molded paper container is subjected to heat treatment in order to make it foam. In the present invention, due to the heat treatment, moisture contained in the paper base material of the body member evaporates, and the thermoplastic resin layer foams to become a foamed thermoplastic resin layer.
The heating temperature and heat time vary depending on the type of paper substrate and thermoplastic resin to be used, and the optimum combination of heating temperature and heating time for the thermoplastic resin to be used can be appropriately determined. A temperature slightly higher than the melting point of the foamed thermoplastic resin (melting point +5 to 10 ° C.) is suitable. Generally, the heating temperature is about 110 ° C. to about 200 ° C., and the heating time is about 1 minute to about 6 minutes. is there. The heating means is not particularly limited, and any means such as hot air, electric heat, or electron beam can be used. If it is heated by hot air or electric heat in a tunnel equipped with a conveyor means, mass production can be performed at low cost.
[その他]
本発明では、所望の効果を損なわない範囲で、必要に応じて、紙製容器の分野で公知の技術を適用することができる。例えば、外壁面となる胴部材の一部に合成樹脂成分を5wt%〜40wt%含有する塗料を塗布し、部分的に発泡を抑制する技術(特許第3014629号公報)、外壁面となる胴部材の表面に発泡と同調して滑らかな印刷面を形成する同調インキを塗布する技術(特許第3408156号公報)、容器胴部材の開口上縁にフランジ部を設ける技術であって、断面角型に強制加工し内側巻き込み端をフランジ部の上部に重合させて二重構造にする技術(特開2001−354226号公報)等が挙げられるが、これらに制限されるものではない。また、印刷適性を高めるために、胴部材の外壁面となる最表層に、顔料とバインダーを主成分とするインキ受理層を設けてもよい。
[Others]
In the present invention, a technique known in the field of paper containers can be applied as necessary within a range that does not impair the desired effect. For example, a technique for applying a paint containing 5 wt% to 40 wt% of a synthetic resin component on a part of a body member serving as an outer wall surface to partially suppress foaming (Japanese Patent No. 3014629), a body member serving as an outer wall surface A technique for applying a synchronized ink that forms a smooth printing surface in synchronization with foaming on the surface of the container (Japanese Patent No. 3408156), and a technique for providing a flange portion at the upper edge of the opening of the container body member, A technique (for example, Japanese Patent Application Laid-Open No. 2001-354226) and the like in which a forcible processing is performed and the inner winding end is superposed on the upper portion of the flange portion to form a double structure may be mentioned, but is not limited thereto. Moreover, in order to improve printability, you may provide the ink receiving layer which has a pigment and a binder as a main component in the outermost layer used as the outer wall surface of a trunk | drum member.
以下、実施例により本発明の効果を詳細に説明する。なお、特にことわらない限り、部および%は重量部および重量%を示す。
[原紙製造例1]
針葉樹晒クラフトパルプ(NBKP;濾水度CSF600ml)10部と広葉樹晒クラフトパルプ(LBKP;濾水度CSF400ml)90部を混合し、混合後の濾水度がCSF420mlのパルプ原料に、内添薬品として固形分で対パルプ絶乾重量当り、硫酸バンド2.5重量%、ロジンサイズ剤0.5重量%、紙力剤としてオイリアクリルアミド0.2重量%を添加し、PHが4.5である原料を、長網抄紙機にて抄速40m/分で単層抄きし、坪量300g/m2、紙厚は341μmの紙匹を作製した。
次いで、得られた紙匹をカレンダーサイジング(線圧30kgf/cm)にて、ポリビニルアルコール(固形分濃度1.5%)を0.4g/m2(絶乾塗工量)塗工し、赤外線ドライヤーにて乾燥後、線圧30kgf/cmでカレンダー処理を行い、水分8.2%の原紙Aを得た。
Hereinafter, the effects of the present invention will be described in detail by way of examples. Unless otherwise specified, parts and% indicate parts by weight and% by weight.
[Base paper production example 1]
10 parts of softwood bleached kraft pulp (NBKP; freeness CSF 600 ml) and 90 parts of hardwood bleached kraft pulp (LBKP; freeness CSF 400 ml) are mixed, and after mixing the pulp raw material having a freeness of CSF 420 ml is used as an internal chemical. Raw material with 2.5% by weight sulfate band, 0.5% by weight rosin sizing agent, 0.2% by weight oil acrylamide as a paper strength agent, and PH of 4.5 per solid dry weight of pulp. Was made into a single layer at a papermaking speed of 40 m / min using a long paper machine to produce a web of paper having a basis weight of 300 g / m 2 and a paper thickness of 341 μm.
Next, the obtained paper web was coated with 0.4 g / m 2 (absolute dry coating amount) of polyvinyl alcohol (solid content concentration 1.5%) by calendar sizing (linear pressure 30 kgf / cm), and infrared rays were applied. After drying with a dryer, calendar treatment was performed at a linear pressure of 30 kgf / cm to obtain a base paper A having a moisture content of 8.2%.
[原紙製造例2]
坪量を270g/m2に変更した以外は、原紙製造例1と同様にして原紙Bを得た。
[Base paper production example 2]
A base paper B was obtained in the same manner as the base paper production example 1 except that the basis weight was changed to 270 g / m 2 .
[原紙製造例3]
坪量を380g/m2に変更した以外は、原紙製造例1と同様にして原紙Cを得た。
[Base paper production example 3]
A base paper C was obtained in the same manner as in the base paper production example 1 except that the basis weight was changed to 380 g / m 2 .
[原紙製造例4]
針葉樹晒クラフトパルプ5部と広葉樹晒クラフトパルプ95部を混合叩解し、混合後の濾水度がCSF410mlのパルプ原料を使用し、カレンダー線圧を20kgf/cmとした以外は、原紙製造例1と同様にして原紙Dを得た。
[Base Paper Production Example 4]
A base paper production example 1 except that 5 parts of softwood bleached kraft pulp and 95 parts of hardwood bleached kraft pulp were mixed and beaten, and a pulp raw material having a freeness of CSF of 410 ml after mixing was used and the calender linear pressure was 20 kgf / cm. Base paper D was obtained in the same manner.
[原紙製造例5]
広葉樹晒クラフトパルプの濾水度をCSF450mlとし、カレンダー線圧を50kgf/cmとした以外は、原紙製造例1と同様にして原紙Eを得た。
[Base Paper Production Example 5]
Base paper E was obtained in the same manner as in base paper production example 1 except that the freeness of hardwood bleached kraft pulp was CSF 450 ml, and the calender linear pressure was 50 kgf / cm.
[原紙製造例6]
広葉樹晒クラフトパルプの濾水度をCSF430mlとした以外は、原紙製造例1と同様にして原紙Fを得た。
[Stencil paper production example 6]
A base paper F was obtained in the same manner as in the base paper production example 1 except that the freeness of hardwood bleached kraft pulp was changed to CSF 430 ml.
[原紙製造例7]
広葉樹晒クラフトパルプの濾水度をCSF410mlとした以外は、原紙製造例1と同様にして原紙Gを得た。
[Base paper production example 7]
Base paper G was obtained in the same manner as in base paper production example 1 except that the freeness of hardwood bleached kraft pulp was changed to 410 ml of CSF.
[原紙製造例8]
広葉樹晒クラフトパルプの濾水度をCSF300mlとした以外は、原紙製造例1と同様にして原紙Hを得た。
[Base paper production example 8]
A base paper H was obtained in the same manner as in base paper production example 1 except that the freeness of hardwood bleached kraft pulp was changed to 300 ml of CSF.
[原紙製造例9]
針葉樹晒クラフトパルプ(NBKP;濾水度CSF600ml)25部と広葉樹晒クラフトパルプ(LBKP;濾水度CSF400ml)75部を混合し、混合後の濾水度がCSF450mlのパルプ原料を使用した以外は、原紙製造例1と同様にして原紙Iを得た。
[Base paper production example 9]
25 parts of softwood bleached kraft pulp (NBKP; freezing degree CSF 600 ml) and 75 parts of hardwood bleached kraft pulp (LBKP; freezing degree CSF 400 ml) were mixed, and a pulp material having a freeness of CSF of 450 ml after mixing was used. Base paper I was obtained in the same manner as in Base Paper Production Example 1.
[原紙製造例10]
広葉樹晒クラフトパルプ(LBKP;濾水度CSF400ml)100部のパルプ原料を使用した以外は、原紙製造例1と同様にして原紙Jを得た。
[Base Paper Production Example 10]
Base paper J was obtained in the same manner as in base paper production example 1 except that 100 parts of pulp material of hardwood bleached kraft pulp (LBKP; freeness CSF 400 ml) was used.
[原紙製造例11]
カレンダー線圧を70kgf/cmとした以外は、原紙製造例1と同様にして原紙Kを得た。
[Base Paper Production Example 11]
A base paper K was obtained in the same manner as in the base paper production example 1 except that the calender linear pressure was 70 kgf / cm.
[原紙製造例12]
カレンダーサイジング線圧を20kgf/cm、カレンダー処理無しとした以外は、原紙製造例1と同様にして原紙Lを得た。
[Base Paper Production Example 12]
A base paper L was obtained in the same manner as in base paper production example 1 except that the calender sizing linear pressure was 20 kgf / cm and no calendering was performed.
[原紙製造例13]
内添薬品として固形分で対パルプ絶乾重量当り、硫酸バンド0.9重量%とした以外は、原紙製造例1と同様にして原紙Mを得た。
[Base Paper Production Example 13]
A base paper M was obtained in the same manner as in the base paper production example 1 except that the solid content was set to 0.9% by weight of the sulfuric acid band per solid dry weight of the pulp as an internal additive.
[原紙製造例14]
内添薬品として硫酸バンドを無添加とした以外は、原紙製造例1と同様にして原紙Nを得た。
[Base Paper Production Example 14]
A base paper N was obtained in the same manner as in base paper production example 1 except that no sulfuric acid band was added as an internal additive.
[原紙製造例15]
カレンダーサイジングによる外添を行わない以外は、原紙製造例1と同様にして原紙Oを得た。
[Base Paper Production Example 15]
A base paper O was obtained in the same manner as in the base paper production example 1 except that no external addition was performed by calendar sizing.
[原紙製造例16]
カレンダーサイジングにて、ポリビニルアルコール(固形分濃度2.0%)を0.9g/m2(絶乾塗工量)塗工した以外は、原紙製造例1と同様にして原紙Pを得た。
[Base Paper Production Example 16]
Base paper P was obtained in the same manner as in Base Paper Production Example 1 except that 0.9 g / m 2 (absolute dry coating amount) of polyvinyl alcohol (solid concentration 2.0%) was applied by calendar sizing.
[原紙製造例17]
カレンダーサイジングにて、酸化澱粉(固形分濃度3.0%)を0.9g/m2(絶乾塗工量)塗工した以外は、原紙製造例1と同様にして原紙Qを得た。
[Base Paper Production Example 17]
Base paper Q was obtained in the same manner as in base paper production example 1 except that the oxidized starch (solid content concentration: 3.0%) was applied at 0.9 g / m 2 (absolute dry coating amount) by calendar sizing.
[原紙製造例18]
2ロールサイズプレスにて、ポリビニルアルコール(固形分濃度0.3%)を0.9g/m2(絶乾塗工量)塗工した以外は、原紙製造例1と同様にして原紙Rを得た。
[Base Paper Production Example 18]
A base paper R was obtained in the same manner as in base paper production example 1 except that polyvinyl alcohol (solid content concentration: 0.3%) was applied at 0.9 g / m 2 (absolute dry coating amount) with a two-roll size press. It was.
[原紙製造例19]
坪量を230g/m2とした以外は、原紙製造例1と同様にして原紙Sを得た。
[Base Paper Production Example 19]
A base paper S was obtained in the same manner as the base paper production example 1 except that the basis weight was 230 g / m 2 .
[原紙製造例20]
広葉樹晒クラフトパルプの濾水度をCSF500mlとし、カレンダー線圧を70kgf/cmとした以外は、原紙製造例1と同様にして原紙Tを得た。
[Base Paper Production Example 20]
A base paper T was obtained in the same manner as in the base paper production example 1 except that the freeness of hardwood bleached kraft pulp was CSF 500 ml and the calendar linear pressure was 70 kgf / cm.
[原紙製造例21]
針葉樹晒クラフトパルプ(NBKP;濾水度CSF600ml)50部と広葉樹晒クラフトパルプ(LBKP;濾水度CSF400ml)50部を混合し、混合後の濾水度がCSF500mlのパルプ原料を使用し、カレンダー線圧を90kgf/cmとした以外は、原紙製造例1と同様にして原紙Uを得た。
[Base Paper Production Example 21]
Mix 50 parts of softwood bleached kraft pulp (NBKP; freeness CSF 600 ml) and 50 parts of hardwood bleached kraft pulp (LBKP; freeness CSF 400 ml), use a pulp raw material with a freeness of CSF 500 ml after mixing, and calendar line A base paper U was obtained in the same manner as in the base paper production example 1 except that the pressure was 90 kgf / cm.
[実施例1〜18、比較例1〜3]
上記で得られた原紙の片面に、紙製容器としたとき胴部材の外壁面となる発泡熱可塑性樹脂層として、融点108℃の低密度ポリエチレン(LDPE)を厚さ70μmとなるように340℃の溶融温度で押出し、この溶融樹脂と原紙とをクーリングロールと硬度70度のニップロールを用いて、線圧15kgf/cmで押圧・圧着した。また、原紙の反対面には、胴部材の内壁面となる非発泡熱可塑性樹脂層として、融点128℃の中密度ポリエチレン(中密度PE)を厚さ40μmとなるように、320℃の溶融温度で押出しラミネートし、胴部材原材料シートを得た。
また、この胴部材原材料シートを、底板部材原材料シート(坪量220g/m2の原紙に中密度ポリエチレンを厚さ40μmとなるように押出しラミネートしたもの)と組み合わせて、直径95mm、高さ115mmの容器を成型し、115℃の乾燥機で4分間加熱し発泡させ、断熱性を有する紙製容器を得た。
[Examples 1-18, Comparative Examples 1-3]
On one side of the base paper obtained above, a low density polyethylene (LDPE) having a melting point of 108 ° C. is formed at 340 ° C. so as to have a thickness of 70 μm as a foamed thermoplastic resin layer that becomes an outer wall surface of the body member when a paper container is used. The molten resin and the base paper were pressed and pressure-bonded at a linear pressure of 15 kgf / cm using a cooling roll and a nip roll having a hardness of 70 degrees. Further, on the opposite surface of the base paper, a non-foamed thermoplastic resin layer serving as the inner wall surface of the body member is melted at 320 ° C. so that a medium density polyethylene (medium density PE) having a melting point of 128 ° C. has a thickness of 40 μm. Was extruded and laminated to obtain a body member raw material sheet.
In addition, this body member raw material sheet is combined with a bottom plate member raw material sheet (a medium density polyethylene extruded on a base paper having a basis weight of 220 g / m 2 and laminated so as to have a thickness of 40 μm), and has a diameter of 95 mm and a height of 115 mm. The container was molded and heated for 4 minutes with a dryer at 115 ° C. for foaming to obtain a paper container having heat insulation properties.
上記の原紙製造例で用いたパルプのろ水度および得られた原紙の紙質評価は、下記のように行った。また、実施例比較例で得られた胴部材原材料シートを用いて、以下の評価試験を行った。原紙製造例1〜18を実施例1〜18とし、原紙製造例19〜21を比較例1〜3として、結果をまとめて表1、表2に示す。 The freeness of the pulp used in the above base paper production examples and the paper quality of the obtained base paper were evaluated as follows. Moreover, the following evaluation tests were performed using the body member raw material sheet obtained in the comparative example. Tables 1 and 2 show the results of the base paper production examples 1 to 18 as Examples 1 to 18 and the base paper production examples 19 to 21 as Comparative Examples 1 to 3, respectively.
<パルプ、紙質の評価>
・カナダ標準ろ水度(CSF) JIS P 8121:1995に従った。
・坪量:JIS P 8124:1998(ISO 536:1995)に従った。
・厚さ:JIS P 8118:1998に従った。
・密度:厚さ、坪量の測定値より算出した。
・紙面PH:原紙を厚さ方向のほぼ中央部で剥離し、JAPPN TAPPI 紙パルプ試験法No.49-2に従い、剥離面を測定した。
・含水率:JIS P 8127に従った。
<Evaluation of pulp and paper quality>
-Canadian Standard Freeness (CSF) JIS P 8121: 1995.
-Basis weight: According to JIS P 8124: 1998 (ISO 536: 1995).
-Thickness: According to JIS P 8118: 1998.
-Density: Calculated from measured values of thickness and basis weight.
-Paper surface PH: The base paper was peeled off at almost the center in the thickness direction, and the peeled surface was measured according to JAPPN TAPPI paper pulp test method No. 49-2.
-Moisture content: According to JIS P 8127.
<離解ろ水度>
発泡した紙製容器の胴部材を2日間以上水に浸漬し、熱可塑性樹脂層を剥離・除去した後、絶乾重量60g分を5cm角の大きさになるように手でちぎって、水に投入して全体の体積を2000mlとした。さらに水に浸漬した状態で一昼夜放置後、TAPPI離解機にて結束繊維がみられない程度まで離解し、20℃に冷却して、JIS−P−8121に準じてCSFを測定した。
<Decomposition freeness>
Immerse the body of the foamed paper container in water for at least 2 days, peel off and remove the thermoplastic resin layer, and then tear off the dry weight of 60 g by hand so that the size is 5 cm square. The total volume was made up to 2000 ml. Further, after being left in a state immersed in water for a whole day and night, it was disaggregated to such an extent that a binding fiber was not observed with a TAPPI disaggregator, cooled to 20 ° C., and CSF was measured according to JIS-P-8121.
<発泡性(発泡樹脂層厚さ)>
発泡後の紙製容器の胴部材の一部を切り出し、発泡した熱可塑性樹脂層の厚さを測定した。
<Foaming (foamed resin layer thickness)>
A part of the body member of the paper container after foaming was cut out, and the thickness of the foamed thermoplastic resin layer was measured.
各実施例、比較例の試験結果から次のことがいえる。
原紙の坪量について、実施例1,2,3、比較例1に着目すると、坪量が低いと発泡性が低く、坪量が多いと発泡性が高くなることがわかる。これらの例では、密度が同じであるので坪量は紙厚に比例しており、含水率も同じであるので、この坪量の差は含有水分量の差でもある。これらを勘案すると、他の要素が共通した場合には、含水量が発泡層の厚さに寄与していると言える。この実施例2の結果では、坪量を270g/m2において、発泡層樹脂層厚が1200μmを実現することができた。
離解ろ水度(CSF)について、実施例1,5〜8、比較例2に着目すると、坪量及び含水量が同じであっても、離解濾水度(CSF)が低くなると発泡が良好になることがわかる。離解濾水度は、原料パルプの濾水度の影響を受ける。そして、これらの例ではLBKPの叩解処理によって調整されている。離解濾水度(CSF)は、360ml以下が適切である。本試験例では、離解濾水度(CSF)が344mlである実施例5では、1210μmの発泡層の厚さが実現できている。
密度について、実施例11、12に着目すると、密度が高い実施例11は低い実施例12よりも発泡厚が小さくなっていることがわかる。この実施例ではカレンダー線圧によって密度に変化を与えている。この密度は蒸発する蒸気の通り易さに影響を与えるものと推測される。密度は各実施例を参考にすると0.91g/cm3まで良好性が確認されている。また、実施例10は、密度を実施例1よりも密度を高めているが、発泡層の厚さを大きくすることができている。これは、パルプ原料の配合をLBKP100%にすることによって、離解濾水度(CSF)を小さくすることができた結果を反映しているものと考えられる。なお、下限値は、前記したように容器用の紙力の確保や熱可塑性樹脂層のラミネート性などの観点に照らして0.6g/cm3が好ましいことが確認されている。
紙面PHは、実施例1、13,14に着目すると、中性側では発泡性が小さくなっている。これは、含水量、密度、坪量などが共通することを考慮すると、中性側では水分が紙に保持されやすく、酸性側では水分が放出されやすいことが起因していると思われる。
外添について、実施例1、15〜17に着目すると、実施例15は実施例1に比べて、発泡層厚はやや大きいが、外観観察によってややムラが見られた。実施例16、17は、実施例に比べて発泡層厚が小さくなっている。これらの結果、外添を多くすると発泡が押さえられる傾向が把握され、全く無いと発泡ムラが発生することが理解できる。PVAや澱粉では0.9g/m2及び0.4g/m2では良好な発泡性が得られている。
また、原料パルプは、NBKPとLBKPを用い、それぞれの特質及び叩解度合いを変えて配合して、試験をした。NBKPは、50%を上限にすることが好ましく、叩解性を上げて使用するには不適当なので、30%以内に押さえることが好ましい。本実施例では0〜25%の配合比で試験をしている。
The following can be said from the test results of the examples and comparative examples.
Focusing on Examples 1, 2, 3 and Comparative Example 1 regarding the basis weight of the base paper, it can be seen that if the basis weight is low, the foamability is low, and if the basis weight is large, the foamability is high. In these examples, since the density is the same, the basis weight is proportional to the paper thickness and the moisture content is the same, so this difference in basis weight is also a difference in moisture content. Considering these, when other elements are common, it can be said that the water content contributes to the thickness of the foamed layer. As a result of Example 2, when the basis weight was 270 g / m 2 , the foamed resin layer thickness was 1200 μm.
Focusing on Examples 1, 5 to 8 and Comparative Example 2 regarding the disaggregation freeness (CSF), even if the basis weight and the water content are the same, foaming is good when the disaggregation freeness (CSF) is low. I understand that The disaggregation freeness is affected by the freeness of the raw pulp. In these examples, adjustment is made by the LBKP beating process. The disaggregation freeness (CSF) is suitably 360 ml or less. In this test example, the foamed layer thickness of 1210 μm can be realized in Example 5 where the disintegration freeness (CSF) is 344 ml.
Focusing on Examples 11 and 12, regarding density, it can be seen that Example 11 having a higher density has a smaller foam thickness than Example 12 having a lower density. In this embodiment, the density is changed by the calendar linear pressure. This density is presumed to affect the ease of evaporating vapor. When the density is 0.91 g / cm 3 with reference to each example, goodness is confirmed. In Example 10, the density is higher than that in Example 1, but the thickness of the foamed layer can be increased. This is considered to reflect the result of reducing the disaggregation freeness (CSF) by setting the blending of the pulp raw material to 100% LBKP. In addition, it has been confirmed that the lower limit is preferably 0.6 g / cm 3 in view of securing the paper strength for containers and laminating properties of the thermoplastic resin layer as described above.
When focusing on Examples 1, 13, and 14, the paper surface PH is less foamable on the neutral side. Considering that the water content, density, basis weight, and the like are common, this is probably because moisture is easily held on paper on the neutral side and moisture is easily released on the acidic side.
Focusing on Examples 1 and 15 to 17 for external addition, Example 15 was slightly larger in thickness than the Example 1, but somewhat uneven by appearance observation. In Examples 16 and 17, the thickness of the foam layer is smaller than that of the example. From these results, it can be understood that when the external addition is increased, the tendency of foaming to be suppressed is grasped, and when there is no external addition, foaming unevenness occurs. With PVA and starch, good foamability is obtained at 0.9 g / m 2 and 0.4 g / m 2 .
Moreover, the raw material pulp was tested by using NBKP and LBKP, blending them with varying characteristics and beating degree. NBKP is preferably set to an upper limit of 50%, and is unsuitable for increasing the beating property, so it is preferable to keep it within 30%. In this example, the test is performed at a blending ratio of 0 to 25%.
1 紙製容器
2 胴部材
3 底板部材
4 紙基材
5 発泡熱可塑性樹脂層
6 発泡セル
7 非発泡熱可塑性樹脂層
DESCRIPTION OF SYMBOLS 1 Paper container 2 Body member 3 Bottom plate member 4 Paper base material 5 Foamed thermoplastic resin layer 6 Foamed cell 7 Non-foamed thermoplastic resin layer
Claims (6)
紙基材の少なくとも片面に熱可塑性樹脂層を形成した原材料シートであって、
該紙基材の坪量が250g/m2以上かつ離解ろ水度がカナダ標準ろ水度で360ml以下であるととともに、
前記熱可塑性樹脂層が紙基材中に含有されている水分の加熱蒸発により発泡されるものであることを特徴とする原材料シート。 In the raw material sheet used for heat insulating paper containers,
A raw material sheet in which a thermoplastic resin layer is formed on at least one side of a paper substrate,
The basis weight of the paper substrate is 250 g / m 2 or more and the disaggregation freeness is a Canadian standard freeness of 360 ml or less,
A raw material sheet, wherein the thermoplastic resin layer is foamed by heating and evaporation of moisture contained in a paper substrate.
胴部材及び/又は底板部材は紙基材の少なくとも片面に熱可塑性樹脂製発泡層を備えた紙製材料を用いた断熱性紙製容器であって、
前記紙基材の坪量が250g/m2以上かつ離解ろ水度がカナダ標準ろ水度で360ml以下であるととともに、
前記熱可塑性樹脂製発泡層が紙基材に含有されている水分を加熱蒸発させて発泡形成された層であることを特徴とする断熱性紙製容器。 In a heat insulating paper container composed of a trunk member and a bottom plate member,
The body member and / or the bottom plate member is a heat insulating paper container using a paper material provided with a thermoplastic resin foam layer on at least one side of a paper substrate,
The basis weight of the paper base material is 250 g / m 2 or more and the disaggregation freeness is a Canadian standard freeness of 360 ml or less,
2. A heat insulating paper container, wherein the thermoplastic resin foam layer is a foamed layer formed by heating and evaporating moisture contained in a paper base material.
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| JP2010065162A (en) * | 2008-09-11 | 2010-03-25 | Japan Polyethylene Corp | Polyethylene resin composition for expandable laminate, and laminate, expansion processed paper, and heat insulating container using the same, and method for producing the same |
| JP2012206384A (en) * | 2011-03-30 | 2012-10-25 | Nippon Paper Industries Co Ltd | Method for producing sheet for container made of heat insulating paper |
| JP2012214962A (en) * | 2011-03-25 | 2012-11-08 | Nippon Paper Industries Co Ltd | Sheet for case made of foamed heat-insulation paper and case made of foamed heat-insulation paper using the same |
| JP2012214038A (en) * | 2011-03-30 | 2012-11-08 | Nippon Paper Industries Co Ltd | Sheet for foam insulation paper container and foam insulation paper container using the same |
| JP2013078928A (en) * | 2011-09-22 | 2013-05-02 | Tosoh Corp | Method for manufacturing expanded laminate and expanded laminate |
| JP2013184729A (en) * | 2012-03-08 | 2013-09-19 | Toppan Printing Co Ltd | Laminate base paper and insulating container using the same |
| JP2014069530A (en) * | 2012-10-01 | 2014-04-21 | Tosoh Corp | Foamed laminate |
| JP2019052382A (en) * | 2017-09-13 | 2019-04-04 | 王子ホールディングス株式会社 | Paper cups and paper cups |
| JP2019123152A (en) * | 2018-01-17 | 2019-07-25 | 王子ホールディングス株式会社 | Paper substrate for foaming heat insulation paper container, sheet for foaming heat insulation paper container, and foaming heat insulation paper container |
| WO2021111902A1 (en) * | 2019-12-04 | 2021-06-10 | 日本製紙株式会社 | Paper foam container for instant food |
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