JPS6382936A - Closed-end seamless molded vessel made of paper and manufacture thereof - Google Patents
Closed-end seamless molded vessel made of paper and manufacture thereofInfo
- Publication number
- JPS6382936A JPS6382936A JP61223868A JP22386886A JPS6382936A JP S6382936 A JPS6382936 A JP S6382936A JP 61223868 A JP61223868 A JP 61223868A JP 22386886 A JP22386886 A JP 22386886A JP S6382936 A JPS6382936 A JP S6382936A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- paper
- container
- paper substrate
- epoxy
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 11
- 229920005989 resin Polymers 0.000 claims description 73
- 239000011347 resin Substances 0.000 claims description 73
- 239000000049 pigment Substances 0.000 claims description 40
- 239000000758 substrate Substances 0.000 claims description 39
- 229920001187 thermosetting polymer Polymers 0.000 claims description 29
- 239000003973 paint Substances 0.000 claims description 21
- 238000000465 moulding Methods 0.000 claims description 17
- 239000004925 Acrylic resin Substances 0.000 claims description 15
- 229920000178 Acrylic resin Polymers 0.000 claims description 15
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical group O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 14
- 239000003822 epoxy resin Substances 0.000 claims description 13
- 229920000647 polyepoxide Polymers 0.000 claims description 13
- 239000006185 dispersion Substances 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 10
- 239000002245 particle Substances 0.000 claims description 9
- 230000035515 penetration Effects 0.000 claims description 9
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 5
- 230000007935 neutral effect Effects 0.000 claims description 4
- 229920001131 Pulp (paper) Polymers 0.000 claims description 3
- 239000004408 titanium dioxide Substances 0.000 claims description 2
- 239000000123 paper Substances 0.000 description 69
- 238000000576 coating method Methods 0.000 description 19
- 239000011248 coating agent Substances 0.000 description 17
- 239000011247 coating layer Substances 0.000 description 15
- 238000010438 heat treatment Methods 0.000 description 8
- 239000007787 solid Substances 0.000 description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 7
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 7
- 239000010410 layer Substances 0.000 description 7
- 238000004513 sizing Methods 0.000 description 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 6
- 235000010215 titanium dioxide Nutrition 0.000 description 6
- -1 alkyl ketene dimer Chemical compound 0.000 description 5
- 239000000835 fiber Substances 0.000 description 5
- 235000013305 food Nutrition 0.000 description 5
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 5
- 229920002554 vinyl polymer Polymers 0.000 description 5
- 239000004593 Epoxy Substances 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000796 flavoring agent Substances 0.000 description 4
- 235000019634 flavors Nutrition 0.000 description 4
- 239000002648 laminated material Substances 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 239000011101 paper laminate Substances 0.000 description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 239000000454 talc Substances 0.000 description 3
- 229910052623 talc Inorganic materials 0.000 description 3
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- 235000015228 chicken nuggets Nutrition 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 229910052570 clay Inorganic materials 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 229910001873 dinitrogen Inorganic materials 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 239000011121 hardwood Substances 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000011256 inorganic filler Substances 0.000 description 2
- 229910003475 inorganic filler Inorganic materials 0.000 description 2
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 2
- 239000000347 magnesium hydroxide Substances 0.000 description 2
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 239000011490 mineral wool Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 235000019645 odor Nutrition 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 238000012856 packing Methods 0.000 description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
- 239000012466 permeate Substances 0.000 description 2
- 239000011122 softwood Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229940014800 succinic anhydride Drugs 0.000 description 2
- XQUPVDVFXZDTLT-UHFFFAOYSA-N 1-[4-[[4-(2,5-dioxopyrrol-1-yl)phenyl]methyl]phenyl]pyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C(C=C1)=CC=C1CC1=CC=C(N2C(C=CC2=O)=O)C=C1 XQUPVDVFXZDTLT-UHFFFAOYSA-N 0.000 description 1
- BJELTSYBAHKXRW-UHFFFAOYSA-N 2,4,6-triallyloxy-1,3,5-triazine Chemical compound C=CCOC1=NC(OCC=C)=NC(OCC=C)=N1 BJELTSYBAHKXRW-UHFFFAOYSA-N 0.000 description 1
- UGIJCMNGQCUTPI-UHFFFAOYSA-N 2-aminoethyl prop-2-enoate Chemical compound NCCOC(=O)C=C UGIJCMNGQCUTPI-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
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
- 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
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- 241000238557 Decapoda Species 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 101100072287 Mus musculus Iffo1 gene Proteins 0.000 description 1
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004962 Polyamide-imide Substances 0.000 description 1
- 239000004642 Polyimide 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
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 239000011358 absorbing material Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- VCNTUJWBXWAWEJ-UHFFFAOYSA-J aluminum;sodium;dicarbonate Chemical compound [Na+].[Al+3].[O-]C([O-])=O.[O-]C([O-])=O VCNTUJWBXWAWEJ-UHFFFAOYSA-J 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- XFWJKVMFIVXPKK-UHFFFAOYSA-N calcium;oxido(oxo)alumane Chemical compound [Ca+2].[O-][Al]=O.[O-][Al]=O XFWJKVMFIVXPKK-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- YGGHJXSSFAFZSO-UHFFFAOYSA-N chloroethene;prop-2-enoic acid Chemical compound ClC=C.OC(=O)C=C.OC(=O)C=C YGGHJXSSFAFZSO-UHFFFAOYSA-N 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 229910001647 dawsonite Inorganic materials 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 238000004070 electrodeposition Methods 0.000 description 1
- 238000009503 electrostatic coating Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- OIAUFEASXQPCFE-UHFFFAOYSA-N formaldehyde;1,3-xylene Chemical compound O=C.CC1=CC=CC(C)=C1 OIAUFEASXQPCFE-UHFFFAOYSA-N 0.000 description 1
- UPSIAUXDGWYOFJ-UHFFFAOYSA-N formaldehyde;furan Chemical compound O=C.C=1C=COC=1 UPSIAUXDGWYOFJ-UHFFFAOYSA-N 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 150000003944 halohydrins Chemical class 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 229920006015 heat resistant resin Polymers 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 238000001000 micrograph Methods 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 125000000466 oxiranyl group Chemical group 0.000 description 1
- 229920003192 poly(bis maleimide) Polymers 0.000 description 1
- 229920003055 poly(ester-imide) Polymers 0.000 description 1
- 229920002312 polyamide-imide Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- AYEFIAVHMUFQPZ-UHFFFAOYSA-N propane-1,2-diol;prop-2-enoic acid Chemical compound CC(O)CO.OC(=O)C=C AYEFIAVHMUFQPZ-UHFFFAOYSA-N 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 238000007761 roller coating Methods 0.000 description 1
- 230000035936 sexual power Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 230000035943 smell Effects 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 235000019640 taste Nutrition 0.000 description 1
- 229920005992 thermoplastic resin Polymers 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
- VSRBKQFNFZQRBM-UHFFFAOYSA-N tuaminoheptane Chemical group CCCCCC(C)N VSRBKQFNFZQRBM-UHFFFAOYSA-N 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
Landscapes
- Containers Having Bodies Formed In One Piece (AREA)
- Making Paper Articles (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Abstract] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
(産業上の利用分![17)
本発明は、紙製有底無継目成形容器及びその製法に関す
るもので、特に電子レンジ、電気オーブン、オーブント
ースタ−等を用いて内容品を加熱、調理できる耐熱性容
器に関する。Detailed Description of the Invention (Industrial Applications! [17) The present invention relates to a bottomed seamless paper molded container and a method for manufacturing the same. This invention relates to a heat-resistant container that can heat and cook the contents.
(従来の技術)
食品等の内容物を手軽に充填し得る容器として、トレー
状の紙容器が広く使用されているが、近年オーブン、電
子レンジ、オーブントースタ−等の普及に伴ない、調理
溶成いは未調理の食品類をトレー状容器に充填して収光
し1食水に際しては、前述した加熱器中に容器ごと入れ
、加熱乃至はクツキングを行い得る容器の開発が望まれ
ている。(Prior art) Tray-shaped paper containers are widely used as containers that can be easily filled with food and other contents, but in recent years, with the spread of ovens, microwave ovens, toaster ovens, etc. In other words, it is desired to develop a container that can be filled with uncooked foods in a tray-like container to collect light, and that can be heated or cooked by placing the entire container in the aforementioned heater for single-serve water. .
このような要望に答えるものとして、特公昭57−41
890号公報には、中性近くで紙料調製を行った後、無
機填剤を含む水性分散液を浸透させて原紙を抄造し1次
いで原紙両面に耐熱性被膜を付着又は貼合形成し、容器
の内側となる面に耐熱性樹脂を塗布することから成る食
品容器用紙の製造方法が記載されている。また、耐熱性
被膜としでは、アルミ箔の他に、ニトロセルローズ系ラ
ッカー、エポキシ系、ウレタン系、フッ素等の樹脂が使
用され、容器内面側には、耐熱性被膜の上に#型剤とし
て、シリコーン系等の#熱性樹脂が施されることも記載
されている。As a response to such requests, the special public
No. 890 discloses that after preparing paper stock at near neutrality, a base paper is made by permeating an aqueous dispersion containing an inorganic filler, and then a heat-resistant coating is attached or laminated on both sides of the base paper. A method of manufacturing paper for food containers is described, which comprises applying a heat-resistant resin to the surface that will become the inside of the container. In addition to aluminum foil, resins such as nitrocellulose lacquer, epoxy, urethane, and fluorine are used as the heat-resistant coating. It is also described that #thermal resin such as silicone type is applied.
(発明が解決しようとする問題点)
この容器は、ウイロ、カステラ等の原料を充填し、20
0乃至250℃程度の温度で加熱処理を行う用途には使
用し得るとしても、オーブントースター等で加熱或いは
クツキングを行う場合には、容器の温度が300℃以上
の高温にも達し、このような高温の用途には耐熱性の点
で未だ十分満足し得るものではなかった。(Problem to be solved by the invention) This container is filled with raw materials such as Uiro, Castella, etc.
Although it can be used for applications that require heat treatment at temperatures of about 0 to 250°C, when heating or baking in a toaster oven, etc., the temperature of the container reaches a high temperature of 300°C or more, and such For high-temperature applications, the heat resistance has not yet been sufficiently satisfactory.
紙のセルロース繊維は、約260℃の温度から炭化及び
着色が開始され、約300℃の温度で完全に炭化する。Paper cellulose fibers begin to carbonize and become colored at a temperature of about 260°C and are completely carbonized at a temperature of about 300°C.
かくして、紙容器を300℃以上の温度に加熱される用
途に使用する場合には、客層自体の外観が使用に耐えな
い程度に黒色に着色すると共に、容器自体の強度も著し
く失われることになるのである。Thus, when paper containers are used in applications where they are heated to temperatures of 300°C or higher, the appearance of the container itself becomes colored black to the extent that it cannot withstand use, and the strength of the container itself is also significantly lost. It is.
紙容器の着色を隠蔽するために、紙基質の表面に、隠蔽
顔料と樹脂結着剤とから成るコート層を設けることが当
然考えられるが、このようなコート紙は一般に成形に必
要な伸びに欠はトレーへのプレス成形性に難点があL、
その成形性を向上させるためにプレス金型を加熱すると
コート層が金型に密着して成形不能となる欠陥を生じ易
い、この成形の問題に加えて、従来のコート紙から成る
トレイ容器は、オーブン中での加熱に際し、悪臭を発生
する傾向があL、食品類の香味(フレーバー)を損うと
いう欠点もある。In order to hide the coloring of paper containers, it is natural to consider providing a coating layer consisting of a hiding pigment and a resin binder on the surface of the paper substrate, but such coated paper generally has a high elongation required for molding. The drawback is that there is difficulty in press forming into the tray.
In addition to this molding problem, when the press mold is heated to improve its moldability, the coating layer adheres to the mold, making molding impossible.In addition to this molding problem, conventional tray containers made of coated paper When heated in an oven, it tends to generate a bad odor and also has the disadvantage of impairing the flavor of foods.
従って、本発明は、成形性に優れた紙積層体から構成さ
れ、容器壁が300°C以上の温度に加熱されたときに
も、外me性、容器強度及び香味保持性に優れている耐
熱性紙容器及びその製法を提供することを課題とする。Therefore, the present invention provides a heat-resistant paper laminate that is composed of a paper laminate with excellent formability and has excellent extrusion properties, container strength, and flavor retention even when the container wall is heated to a temperature of 300°C or higher. The purpose of the present invention is to provide a flexible paper container and a method for manufacturing the same.
(問題点を解決するための手段)
本発明者等は、紙基質に樹脂と隠蔽顔料とを含有するコ
ート層を塗布する場合、樹脂として熱硬化性樹脂を用い
、しかもこの熱硬化性樹脂を水性分散体あるいは水溶性
の形で施すと、有機溶液型の塗料を施す場合に生じる紙
基質内部への滲透がが防止され、その結果として紙積層
体の加工性が顕著に向上すると共に、積層体の耐熱性も
著しく向上することを見出した。(Means for Solving the Problems) The present inventors used a thermosetting resin as the resin when coating a paper substrate with a coating layer containing a resin and a hiding pigment. When applied in aqueous dispersion or water-soluble form, the seepage into the paper substrate that occurs when applying organic solution-based paints is prevented, and as a result the processability of paper laminates is significantly improved and the laminate It was also found that the body's heat resistance was significantly improved.
即ち、本発明は、紙基質と紙基質の少なくとも一方の表
面に設けられた樹脂コート層とから成る有底無継目成形
容器において、樹脂コート層が熱硬化性樹脂と隠蔽顔料
とを含有して成L、該樹脂コート層は積層体の厚さをし
、該コート層表面から紙2!i賀内への浸透深さをIと
したとき、 g/L<0.1を満足するように設けられ
ていることを特徴とする有底無継目成形容器に関する。That is, the present invention provides a bottomed seamless molded container comprising a paper substrate and a resin coat layer provided on at least one surface of the paper substrate, wherein the resin coat layer contains a thermosetting resin and a hiding pigment. The resin coat layer has the same thickness as the laminate, and the paper 2! The present invention relates to a seamless molded container with a bottom, characterized in that the container is configured to satisfy g/L<0.1, where I is the depth of penetration into the interior of the container.
本発明は更に、分散質として隠蔽顔料と平均粒径0.0
5乃至1.0pmの熱硬化性樹脂とを含む水性分散体を
、紙基質の少なくとも一方の表面に塗布し、塗布層を乾
燥し、熱硬化性樹脂を硬化させ。The present invention further includes a concealing pigment as a dispersoid and an average particle size of 0.0.
An aqueous dispersion containing 5 to 1.0 pm of thermosetting resin is applied to at least one surface of the paper substrate, the coated layer is dried, and the thermosetting resin is cured.
得られる積層体を有底無継目容器形状にプレス成形する
ことを特徴とする紙製有底無継目成形容器の製法に関す
る。The present invention relates to a method for manufacturing a seamless molded paper container with a bottom, which comprises press-molding the obtained laminate into the shape of a seamless container with a bottom.
本発明は更にまた、分散質として隠蔽顔料を含み、樹脂
成分として水溶性型の熱硬化性エポキシ−アクリル系樹
脂を含む水性塗料を、紙2!質の少なくとも一方の表面
に塗布し、塗布層を乾燥し、熱硬化性樹脂を硬化させ、
得られる積層体を有底無継目容器形状にプレス成形する
ことを特徴とする紙製有底無継目成形容器の製法にも関
する。The present invention further provides paper 2! a water-based paint containing a hiding pigment as a dispersoid and a water-soluble thermosetting epoxy-acrylic resin as a resin component. The thermosetting resin is applied to at least one surface of the resin, the applied layer is dried, and the thermosetting resin is cured.
The present invention also relates to a method for producing a seamless molded paper container with a bottom, which comprises press-molding the obtained laminate into the shape of a seamless container with a bottom.
(作 用)
本発明の耐熱性紙容器を斜視図で示す第1図において、
このトレイ状の紙容器は、矩形で平面状の底壁部1と、
この底壁部1に連なる側壁部2a、2b、2c、2dと
から成っておL、隣接する側壁部間にはひだ部3があL
、且つ側壁部の上端縁にはフランジ部乃至カール部4が
設けられている。(Function) In FIG. 1 showing a perspective view of the heat-resistant paper container of the present invention,
This tray-shaped paper container includes a rectangular and flat bottom wall portion 1;
It consists of side walls 2a, 2b, 2c, and 2d that are connected to the bottom wall 1, and there are folds 3 between the adjacent side walls.
, and a flange portion or curl portion 4 is provided at the upper end edge of the side wall portion.
この紙容器の器壁断面構造を拡大して示す第2図におい
て、この器壁10は、紙基質11と紙基質の両表面に施
された耐熱性被覆層12a 、 12bとから成ってい
る。In FIG. 2, which shows an enlarged cross-sectional structure of the wall of this paper container, the wall 10 is made up of a paper substrate 11 and heat-resistant coating layers 12a and 12b applied to both surfaces of the paper substrate.
本発明においては、この耐熱性被覆層12a、 12b
を隠蔽顔ネ4と熱硬化性樹脂とから形成する。先ず、こ
の隠蔽顔料は、紙基質11と加熱された高温雰囲気とを
熱的に遮断して、紙基質の加熱下での強度低下傾向を少
ないレベルに維持する作用を行うと共に、被覆自体にも
耐熱性を付与し且つ紙基質に生成するta維炭化物を隠
蔽して外観を良好に維持する作用を行う、更に、塗料中
に含有される隠蔽顔料は、金型表面における樹脂粘着物
の生成及び蓄積を幾分減少させて成形性を向上させる補
助的作用をも行う。In the present invention, these heat-resistant coating layers 12a, 12b
is formed from a concealing face mask 4 and a thermosetting resin. First, the hiding pigment thermally isolates the paper substrate 11 from the heated high-temperature atmosphere, thereby maintaining the paper substrate's tendency to decrease in strength under heating to a small level, and also acts on the coating itself. The concealing pigment contained in the paint has the effect of imparting heat resistance and maintaining a good appearance by concealing the TA fiber carbonized substances generated on the paper substrate.Furthermore, the concealing pigment contained in the paint prevents the formation of resin stickiness on the surface of the mold. It also serves the auxiliary action of somewhat reducing build-up and improving moldability.
この隠蔽顔料は、樹脂結着剤を介して紙基質表面に保持
されるが、この結着剤は熱硬化性樹脂でなければならな
い、先ず、この被覆12a、12bとして熱可塑性樹脂
を用いるときには、容器へのプレス成形に際して、この
被覆が金型へ密着する等の成形上の不都合を生じ易く、
またオーブン等での加熱に際して悪臭、異味、異臭を発
生して食品類の香味(フレーバー)を損うと共に、容器
強度自体も低下する傾向が著しいが、この結着剤成分を
熱硬化型樹脂とすることによL、上述した不都合を解消
乃至軽減することができる。The hiding pigment is retained on the paper substrate surface via a resin binder, which must be a thermosetting resin. First, when using a thermoplastic resin as the coatings 12a, 12b, When press-molding into a container, this coating tends to cause molding problems such as sticking to the mold,
In addition, when heated in an oven, etc., bad smells, strange tastes, and strange odors are generated, which impairs the flavor of foods, and there is a marked tendency for the strength of the container itself to decrease. By doing so, the above-mentioned disadvantages can be eliminated or alleviated.
被覆層12a、12bの形成に際して、分散質として隠
蔽顔料と平均粒径0.05乃至1.0ルmの熱硬化性樹
脂とを含む水性分散体を用いるか、あるいは分散質とし
て隠蔽顔料を含み、樹脂成分として水溶性型の熱硬化性
エポキシ−アクリル系樹脂を含む水性塗料を用いること
が第二の特徴である。従来、顔料及び熱硬化性樹脂を含
有する塗料は、殆んどの場合有機溶媒溶液として使用さ
れる。しかしながら、既に指摘した通L、有機溶液タイ
プの塗料を紙基質に塗布する場合には熱硬化性樹脂が紙
基質内部に深く滲透するのを避は得ない、これに対して
、本発明では隠蔽顔料及び熱硬化性樹脂を水性分散体の
形で施すか、あるいは熱硬化性樹脂を水溶性の形で施す
ことにより熱硬化性樹脂の紙基体内への滲透の程度を著
しく小さくすることができる。When forming the coating layers 12a and 12b, an aqueous dispersion containing a hiding pigment and a thermosetting resin with an average particle size of 0.05 to 1.0 lm is used as a dispersoid, or an aqueous dispersion containing a hiding pigment as a dispersoid is used. The second feature is that a water-based paint containing a water-soluble thermosetting epoxy-acrylic resin as a resin component is used. Traditionally, paints containing pigments and thermosetting resins are mostly used as solutions in organic solvents. However, as already pointed out, when an organic solution type paint is applied to a paper substrate, it is unavoidable that the thermosetting resin penetrates deeply into the paper substrate. By applying the pigment and thermosetting resin in the form of an aqueous dispersion, or by applying the thermosetting resin in water-soluble form, the degree of penetration of the thermosetting resin into the paper substrate can be significantly reduced. .
即ち、器壁(積層体)10の厚さをL、樹脂コート層1
2a(12b)の表面からの滲透深さを2としたとき、
本発明によれば、I!、/Lを0.1よりも小、好適に
は0.015乃至0.08の範囲内に抑制することがで
きる。That is, the thickness of the vessel wall (laminate) 10 is L, the resin coating layer 1
When the penetration depth from the surface of 2a (12b) is 2,
According to the invention, I! , /L can be suppressed to less than 0.1, preferably within the range of 0.015 to 0.08.
但し、滲透深さlは紙質の状態により最大深さと最小深
さの間に差を生ずる場合があるが、この場合は平均滲透
深さをlとすべきである。However, the penetration depth l may differ between the maximum depth and the minimum depth depending on the condition of the paper quality, but in this case, the average penetration depth should be l.
このように水性分散型あるいは水溶性型の樹脂を用いる
ことによL、樹脂コート層12a、12bの滲透深さを
小さな値に抑制できる理由としては次のようなものが考
えられる。即ち、本発明における紙基質にはアルキルケ
テンダイマーやアルケニル無水コハク酸などの中性サイ
ズ剤やロジン系でも硫酸バンドの量を少なくした弱酸性
処方のサイズ剤が使用されている。サイズ処理は紙に耐
水性を与えるため、すなわち紙の表面がぬれても紙の内
部へ水の滲透を防止するために行われている。従って、
本発明におけるように水を媒体する水性塗料を紙基質に
塗布した場合、サイズ剤の効果により紙基体内への樹脂
の滲透の程度が著しく抑制されるのである。また、紙は
一般に繊維間の間隙から工部作用によって水や有機溶媒
を吸収するので、樹脂が繊維間間隙より大きい水性分散
体であれば、紙基体内への樹脂の滲透はさらに抑えられ
ることになる。The following are possible reasons why the penetration depth of L and the resin coat layers 12a and 12b can be suppressed to a small value by using a water-based dispersion type or water-soluble type resin. That is, the paper substrate in the present invention uses a neutral sizing agent such as an alkyl ketene dimer or alkenyl succinic anhydride, or a rosin-based sizing agent with a weakly acidic formulation that has a reduced amount of sulfuric acid bands. Sizing treatment is performed to make paper water resistant, that is, to prevent water from seeping into the paper even if the surface of the paper gets wet. Therefore,
When a water-based paint containing water as a medium is applied to a paper substrate as in the present invention, the degree of seepage of the resin into the paper substrate is significantly suppressed due to the effect of the sizing agent. Additionally, since paper generally absorbs water and organic solvents through the gaps between the fibers through mechanical action, if the resin is an aqueous dispersion larger than the gaps between the fibers, seepage of the resin into the paper base can be further suppressed. become.
一方、イT機溶媒系の塗料を使用した場合、サイズ剤は
有機溶媒の滲透を抑制する効果を持たないため、紙基体
内の深くまで塗料が滲透することになる。On the other hand, when a solvent-based paint is used, the paint permeates deep into the paper substrate because the sizing agent does not have the effect of suppressing seepage of the organic solvent.
また、本発明において、樹脂コート層12a。Moreover, in the present invention, the resin coat layer 12a.
12bの滲透深さを小さな値に抑制することによL、積
層体の成形性が向上し且つ#熱性も向上する理由は次の
ようなものと考えられる。即ち、紙積層体のプレス成形
性は、紙基質中で紙繊維が適度に相互に絡み合い乃至交
叉しておL、適度の伸びが保持されていることに帰因す
るものと認められるが、熱硬化性樹脂が内部に深く滲透
した場合には、絡み合い部乃至交叉部が固定され、紙基
質の伸びが失われるために、プレス成形性が失われるも
のと認められる。これに対して、本発明による積層体で
は熱硬化性樹脂の滲透深さが極く浅く、紙基質の本来の
伸びが保持され、その結果として良好なプレス成形性が
保全されるものと思われる。また、熱硬化性樹脂の紙基
質内への滲透が抑制されることによL、紙基質の表面に
デンス(濃密)な状態で熱遮断膜が形成されることによ
L、積層体の耐熱性が向上するものと認められる。The reason why the moldability of the laminate is improved and the thermal properties are also improved by suppressing the penetration depth of 12b to a small value is considered to be as follows. In other words, it is recognized that the press formability of paper laminates is due to the paper fibers being moderately intertwined or crossing each other in the paper substrate, and maintaining a moderate elongation. If the curable resin permeates deeply into the interior, the intertwined or intersecting parts become fixed and the elongation of the paper substrate is lost, resulting in a loss of press formability. On the other hand, in the laminate according to the present invention, the penetration depth of the thermosetting resin is extremely shallow, and the original elongation of the paper substrate is maintained, and as a result, it is thought that good press formability is maintained. . In addition, the permeation of the thermosetting resin into the paper substrate is suppressed, and the formation of a dense heat-blocking film on the surface of the paper substrate increases the heat resistance of the laminate. It is recognized that this improves sexual performance.
(発明の作用効果)
本発明によれば、紙基質の表面に隠蔽顔料と熱硬化性樹
脂とを含むコート層を、紙基質内への滲透を抑制しなが
ら設けたことによL、容器への優れた成形性が得られ、
容器壁が300℃以上の温度に加熱された場合にも容器
の外観特性、容器強度及び香味保持性を顕著に向上させ
ることが可能となL、電子レンジ及びオーブントースタ
−の両方の用途に供し得るデュアルオーブナブル容器が
提供できた。(Operations and Effects of the Invention) According to the present invention, a coating layer containing a hiding pigment and a thermosetting resin is provided on the surface of a paper substrate while suppressing permeation into the paper substrate. Excellent formability is obtained,
It is possible to significantly improve the appearance characteristics, container strength, and flavor retention of the container even when the container wall is heated to a temperature of 300°C or higher, and can be used in both microwave ovens and toaster ovens. We were able to provide dual ovenable containers to get the job done.
(発明の詳細な説明)
へ鼠也血凰1
本発明においては、任意の熱硬化性樹脂、フェノール・
ホルムアルデヒド樹脂、フラン−ホルムアルデヒド樹脂
、キシレン−ホルムアルデヒド樹脂、ケトン−ホルムア
ルデヒド樹脂、尿素ホルムアルデヒド樹脂、メラミン−
ホルムアルデヒド樹脂、アルキド樹脂、不飽和ポリエス
テル樹脂、エポキシ樹脂、ビスマレイミド樹脂、トリア
リルシアヌレート樹脂、熱硬化型アクリル樹脂、シリコ
ーン樹脂等の単独又は2種以上の組合せが使用される。(Detailed Description of the Invention) In the present invention, any thermosetting resin, phenol,
Formaldehyde resin, furan-formaldehyde resin, xylene-formaldehyde resin, ketone-formaldehyde resin, urea-formaldehyde resin, melamine-
Formaldehyde resins, alkyd resins, unsaturated polyester resins, epoxy resins, bismaleimide resins, triallyl cyanurate resins, thermosetting acrylic resins, silicone resins, and the like may be used alone or in combination of two or more.
これらの内でも、本発明では、エポキシ樹脂と、エポキ
シ樹脂に対して反応性を有する基、例えばカルボキシル
基、水酸基、アミノ基等の官能基を有する反応性アクリ
ル樹脂及び/又はビニル樹脂との組合せである。これら
のエポキシ/アクリル又はエポキシ/ビニル塗料は、架
橋された条件下で加工性に優れていると共に、金型表面
への粘着物形成が少ないという点で本発明の目的に特に
適したものである。Among these, in the present invention, a combination of an epoxy resin and a reactive acrylic resin and/or vinyl resin having a functional group such as a carboxyl group, a hydroxyl group, or an amino group, such as a group reactive with the epoxy resin, is preferred. It is. These epoxy/acrylic or epoxy/vinyl coatings are particularly suitable for the purposes of the present invention in that they have excellent processability under crosslinked conditions and less stickiness formation on mold surfaces. .
エポキシ樹脂成分としては、ビスフェノールAとエビハ
ロヒドリンとを縮合させることにより得た芳香族エポキ
シ樹脂が特に適しておL、そのエポキシ当量は一般に1
000乃至4000の範囲内にあるものがよい、アクリ
ル樹脂としては、前記官能基を与える単量体成分として
、メタクリル猷、アクリル酸、無水マレイン酸のような
不飽和カルボン酸又はその無水物; (メタ)アクリル
酸−2−ヒドロキシエチルエステル、(メタ)アクリル
酸−2−ヒドロキシプロピルエステル等のとドロキシ基
含有単量体; (メタ)アクリル酸−2−アミノエチル
エステル、(メタ)アクリル酸=2−N、N−ジエチル
アミノエチルエステル、(メタ)アクリル酸−N−アミ
ノエチル−アミノエチルエステル等の7ミノ基含有量体
の少なくとも1種と、(メタ)アクリル酸アルキルエス
テル(例えばメチルメタクリレート、エチルアクリレー
ト等)の少なくとも1種と、所望によりスチレン等を含
む共重合体が挙げられる。また、ビニル樹脂としては、
塩化ビニル−無水マレイン酸共重合体、塩化ビニル−ア
クリル酸−アクリル酸エステル共重合体、塩化ビニル−
酢酸ビニル共重合体部分ケン化物、塩化ビニル−無水マ
レイン酸スチレン共重合体、塩化ビニル−メタクリル酸
−酢酸ビニル共重合体ケン化物等のカルボキシル基及び
/又は水酸基含有ビニル樹脂を挙げることができる。As the epoxy resin component, an aromatic epoxy resin obtained by condensing bisphenol A and shrimp halohydrin is particularly suitable, and its epoxy equivalent is generally 1.
For the acrylic resin, the monomer component providing the functional group may be an unsaturated carboxylic acid such as methacrylic acid, acrylic acid, or maleic anhydride, or an anhydride thereof; ( Doroxy group-containing monomers such as meth)acrylic acid-2-hydroxyethyl ester and (meth)acrylic acid-2-hydroxypropyl ester; (meth)acrylic acid-2-aminoethyl ester and (meth)acrylic acid = 2-N,N-diethylaminoethyl ester, (meth)acrylic acid-N-aminoethyl-aminoethyl ester, etc., at least one type of heptamine group-containing substance, and (meth)acrylic acid alkyl ester (for example, methyl methacrylate, Examples include copolymers containing at least one type of ethyl acrylate, etc.) and, if desired, styrene. In addition, as a vinyl resin,
Vinyl chloride-maleic anhydride copolymer, vinyl chloride-acrylic acid-acrylic acid ester copolymer, vinyl chloride-
Examples include vinyl resins containing carboxyl groups and/or hydroxyl groups, such as partially saponified vinyl acetate copolymers, vinyl chloride-styrene maleic anhydride copolymers, and saponified vinyl chloride-methacrylic acid-vinyl acetate copolymers.
これらの樹脂は、樹脂粒子の径が0.05乃至1.0延
の水性分散体、特に界面活性剤で乳化された、或いは自
己乳化した水性乳化液の形また。水溶性の形、更にこれ
らの組合せた形で使用される。These resins may be in the form of an aqueous dispersion in which resin particles have a diameter of 0.05 to 1.0 mm, particularly in the form of an aqueous emulsion emulsified with a surfactant or self-emulsified. It is used in water-soluble forms as well as in combinations thereof.
これらの内でも、本発明の目的には、エポキシ−アクリ
ル樹脂、特に自己乳化型エポキシ−アクリル樹脂を用い
ることが好ましい、このようなエポキシ−アクリル樹脂
の適当な例として、アクリル酸もしくはメタクリル酸1
2乃至3Oi量%、およびスチレン、メチルスチレン、
ビニルトルエンまたはアクリル酸もしくはメタクリル酸
の炭素数1ないし8のアルキルエステルの1種もしくは
2種以上70ないし88重量%を共瓜合せしめた数平均
分子、310,000ないし100,000のアルカリ
中和型アクリル系樹脂(A)、並びに1分子中に平均1
.1個ないし2,0個のエポキシ基を有する数平均分子
量1,400以上の芳香族系エポキシ樹脂(B)を反応
せしめた残存オキシラン環を有するカルボキシ基過剰の
エポキシ樹脂、アクリル;v8樹脂部分反応物を最終被
覆組成物のpHが5ないし11となる量のアンモニアも
しくはアミンの存在下に水性媒体中に分散せしめたもの
が挙げられる。Among these, for the purpose of the present invention, it is preferable to use epoxy-acrylic resins, particularly self-emulsifying epoxy-acrylic resins. Suitable examples of such epoxy-acrylic resins include acrylic acid or methacrylic acid 1.
2 to 3 Oi amount%, and styrene, methylstyrene,
A number-average molecule containing 70 to 88% by weight of one or more of vinyltoluene or an alkyl ester having 1 to 8 carbon atoms of acrylic acid or methacrylic acid, neutralized with an alkali of 310,000 to 100,000. type acrylic resin (A), and an average of 1 per molecule
.. Epoxy resin with an excess of carboxyl groups and acrylic having residual oxirane rings reacted with an aromatic epoxy resin (B) having a number average molecular weight of 1,400 or more and having 1 to 2.0 epoxy groups; acrylic; v8 resin partial reaction Dispersed in an aqueous medium in the presence of an amount of ammonia or amine such that the pH of the final coating composition is between 5 and 11.
また、アクリル系樹脂とエポキシ樹脂の比率を例えば8
対2や9対1のようにアクリル系樹脂の比率を多くし、
アルコール系溶媒を少量添加することにより水溶性型と
したものも挙げられる。Also, the ratio of acrylic resin and epoxy resin may be set to 8, for example.
Increase the ratio of acrylic resin such as 2:2 or 9:1,
Examples include those made water-soluble by adding a small amount of alcoholic solvent.
さらに水溶性型の樹脂と水性乳化型の樹脂の組み合わせ
たものも用いることができる。Furthermore, a combination of a water-soluble resin and an aqueous emulsion resin can also be used.
隠蔽顔料
隠蔽顔料としては、無毒性、或いは低毒性で、隠蔽力の
大きい顔料、特に隠蔽力(JISK 5101)が40
以下の顔料が使用される。適当な顔料の例は次の通りで
ある。Hiding Pigments Hiding pigments include non-toxic or low toxicity pigments with a high hiding power, especially those with a hiding power (JISK 5101) of 40.
The following pigments are used: Examples of suitable pigments are:
これらの顔料は単独でも或いは2種以上の組合せでも使
用されるが、好適な顔料は、ルチル型或いはアナターゼ
型のチタンホワイト(二酸化チタン)を主体とするもの
である。勿論、チタンホワイトを単独で使用する代りに
、例えば黄色酸化鉄やベンガラ或いは群青の少量を配合
して、クリーム色、淡いピンク色、淡い青色等の着色コ
ート層としてもよい、更に、この顔料に対して、水酸化
アルミニウム、水酸化マグネシウム、タルク、クレイ、
ケイ酩マグネシウム、ケイ酸カルシウム等の充填剤乃至
は増量剤を併用することができる。These pigments may be used alone or in combination of two or more types, but the preferred pigment is one mainly composed of rutile type or anatase type titanium white (titanium dioxide). Of course, instead of using titanium white alone, for example, a small amount of yellow iron oxide, red iron oxide, or ultramarine may be blended to create a colored coating layer of cream color, pale pink, pale blue, etc. On the other hand, aluminum hydroxide, magnesium hydroxide, talc, clay,
Fillers or extenders such as magnesium silicate and calcium silicate may be used in combination.
紙71(質
紙としては、針葉樹パルプ、広葉樹パルプ等の天然パル
プ、ガラス繊維、ロックウール、スラグウール、アスベ
スト、セラミック繊維等の無機繊維;ポリオレフィン、
ポリエステル、ポリアミド、ポリイミド等の合成樹脂パ
ルプの1種又は2種以上を抄造して得られる天然又は合
成紙を挙げることができる。これらの紙には難燃料兼填
主1を配合することができ、例えば水酸化アルミニウム
、水酸化マグネシウム、アルミン酸カルシウム、ドーソ
ナイト等を挙げることができる。また1紙の風合い、腰
等を向上させる目的でシリカ、タルク、クレイ、炭酸カ
ルシウム等を配合することができ、更に抄造性を改善し
、1i!AM相互の結合乃至固定を行うために、有機樹
脂バインダーを用いることができる0本発明においては
、木材パルプから得られる通常の紙を用いた場合にも、
wJ茗に優れた#熱性を賦芋し得ることが利点である0
紙基質の坪量は100乃至600 g/m2、特に15
0乃至400 germ2の範囲内にあることが望まし
い。Paper 71 (quality paper includes natural pulp such as softwood pulp and hardwood pulp, inorganic fibers such as glass fiber, rock wool, slag wool, asbestos, and ceramic fiber; polyolefin,
Examples include natural or synthetic paper obtained by paper-making one or more synthetic resin pulps such as polyester, polyamide, and polyimide. These papers can be blended with a fuel-resistant filler 1, such as aluminum hydroxide, magnesium hydroxide, calcium aluminate, dawsonite, and the like. In addition, silica, talc, clay, calcium carbonate, etc. can be added to improve the texture, stiffness, etc. of 1 paper, which further improves papermaking properties and improves 1i! In order to bond or fix AM to each other, an organic resin binder can be used. In the present invention, even when ordinary paper obtained from wood pulp is used,
wJ has an advantage of having excellent heat resistance.0
The basis weight of the paper substrate is between 100 and 600 g/m2, especially 15
It is desirable that it be within the range of 0 to 400 germ2.
耐熱性の点では1弱酸性紙や中性紙、特にアルキルケテ
ンダイマー、アルケニル無水コハク酸等をサイズ剤とし
て用いた中性紙が特に好ましい。In terms of heat resistance, slightly acidic paper or neutral paper, particularly neutral paper using an alkyl ketene dimer, alkenyl succinic anhydride, etc. as a sizing agent, is particularly preferred.
積層材料の製造
本発明に用いる積層材料は、前述した熱硬化性樹脂と隠
蔽顔料とを含有する水性塗布液を調製し、この塗布液を
紙、S質の両面に塗布し、形成される被覆を硬化させる
ことにより得られる。Manufacture of laminated material The laminated material used in the present invention is produced by preparing an aqueous coating solution containing the above-mentioned thermosetting resin and concealing pigment, and applying this coating solution to both sides of paper and S material. Obtained by curing.
熱硬化性樹脂と隠蔽顔料との比率は種々変化させ得るが
、被覆層の樹脂が下記式
%式%(1)
式中、○^は隠蔽顔料の吸油材(If/1oog)であ
L、dRは樹脂の密度(g/mf)を表わし、
kは0.005乃至0.2の数である、を満足するff
1ffi比(Rp )で存在することがよい。Although the ratio of the thermosetting resin and the hiding pigment can be varied, the resin of the coating layer has the following formula % formula % (1) In the formula, ○^ is the oil absorbing material of the hiding pigment (If/1oog) L, dR represents the density of the resin (g/mf), k is a number from 0.005 to 0.2, and ff satisfies the following.
It is preferable to exist at a ratio of 1ffi (Rp).
水明細書において、前記式(1)は次の意味を有する。In the specification, the formula (1) has the following meaning.
式(1)の右辺におけるOAは隠蔽顔料の吸油量(ml
/ 100g)であL、これと樹脂の密度dRとの積
は、樹脂が連続相及び顔料が分散相となった均質組成物
を形成し得るという範囲内で、顔料100g当りの結着
剤のグラム数を意味する。従って、この組成物をガラス
板のような平滑で不浸透性の基体表面へ塗布すると式(
1)の右辺におけるkの値が0.01以上では顔料粒子
が外表面に露出することなく内部にも空隙や表面付近に
凹凸のないコート層が形成され、kの値が0.01未満
の場合には顔料粒子が外表面に露出し、或いは内部にも
空隙や表面付近に凹凸のあるコート層が形成されること
になる。OA on the right side of equation (1) is the oil absorption amount of the hiding pigment (ml
/ 100 g) L, and the product of this and the density dR of the resin is the amount of binder per 100 g of pigment, to the extent that a homogeneous composition can be formed in which the resin is a continuous phase and the pigment is a dispersed phase. It means the number of grams. Therefore, when this composition is applied to a smooth, impermeable substrate surface such as a glass plate, the formula (
When the value of k on the right side of 1) is 0.01 or more, the pigment particles are not exposed on the outer surface, and a coating layer is formed inside without voids or irregularities near the surface. In this case, the pigment particles are exposed on the outer surface, or a coating layer with voids or unevenness is formed inside the pigment particles near the surface.
式(1)のkの値が0.2以下となる対顔料樹脂重量比
(Rp )では、顔料粒子が外表面に露出し或いは内部
にも空隙や表面近くに凹凸のあるコート層が形成され、
このようなコート層を有する積層体では、紙基体と同様
の伸びを有し、トレー形状への成形が容易に行われるの
である0式(1)のkの値には5紙基体への隠蔽顔料の
付着力の点で一定の最低基準値があL、kの値が0.0
05を下廻ると隠蔽顔料の成形時における離脱等が生じ
、また器壁の#熱強度も低下するようになるのである。At a pigment-to-resin weight ratio (Rp) where the value of k in formula (1) is 0.2 or less, the pigment particles are exposed on the outer surface, or a coating layer with voids or unevenness is formed inside the pigment particles near the surface. ,
A laminate having such a coating layer has the same elongation as the paper substrate and can be easily formed into a tray shape. In terms of pigment adhesion, there is a certain minimum standard value of L, and the value of k is 0.0.
If the value falls below 05, the hiding pigment may come off during molding, and the #thermal strength of the vessel wall also decreases.
塗布液の固形分濃度は、均一塗布性が得られる範囲内で
水の竜の可及的に低いものであL、一般に20乃至80
重量り6の範囲が適8である。The solid content concentration of the coating liquid is as low as possible within the range that allows uniform coating, and is generally 20 to 80 L.
The range of weight 6 is suitable.
塗71にはスプレー塗装、静電塗装、ローラーコーティ
ング、グラビアロールコーティング、浸漬塗装、電着塗
装等の塗布手段が使用される。For the coating 71, coating means such as spray coating, electrostatic coating, roller coating, gravure roll coating, dip coating, and electrodeposition coating are used.
紙基体への塗工量は、固形分として2乃至30112/
g、特に5乃至20m2/gとすることによL、満足す
べき耐熱性と加工性との組合せが得られる。The coating amount on the paper substrate is 2 to 30112/2 as solid content.
By setting L to 5 to 20 m2/g, a satisfactory combination of heat resistance and workability can be obtained.
形成される被覆の硬化は、触媒、加熱或いは紫外線又は
放射線照射等のそれ自体公知の手段で行われる。Curing of the coating formed takes place by means known per se, such as catalysis, heating or irradiation with ultraviolet light or radiation.
容器への成形
トレイ、ボウル、カップ等の有底無継目容器への成形は
、雄型及び雌型を加熱し、これらの間に積層材料を供給
し、プレス成形することにより行われる。金型を加熱す
ることによL、積層材料の成形は未加熱の金型を使用す
る場合に比して飛躍的に向上する。金型の加熱温度は、
一般に50乃至180°C1特に90乃至150°Cの
範囲とするのが望ましい。Forming into containers Forming into bottomed seamless containers such as trays, bowls, and cups is performed by heating a male mold and a female mold, supplying a laminated material between them, and press-molding. By heating the mold, the molding of the laminated material is dramatically improved compared to when an unheated mold is used. The heating temperature of the mold is
In general, it is desirable that the temperature be in the range of 50 to 180°C, particularly 90 to 150°C.
本発明を次の例で説明する。The invention is illustrated by the following example.
実施例1゜
まず次の手順によりチタンホワイトを隠蔽顔料として含
む水性エポキシ−アクリル系塗料を調製した。Example 1 First, a water-based epoxy-acrylic paint containing titanium white as a hiding pigment was prepared by the following procedure.
(A)カルボキシル基含有アクリル系樹脂の製造スチレ
ン 300.0部アクリル酸エチル
210.0メタクリルm
90.0過酸化ベンゾイル 1
2.0上記組成の混合物の嵐を窒素ガス置換した4ツロ
フラスコに仕込み80〜90℃に加熱し、その温度に保
ちつ覧残りの3八を2時間かけて徐々に滴下し、滴下終
了後、更にその温度で2時間かきまぜた後冷却し、酸価
93(固形分換算、以下同じ)、固形分59.7%、粘
度4100cps(25℃、以下粘度はすべて25°C
におけるΔIII定結果全結果)カルボキシル基含有樹
脂溶液を得た。(A) Production of carboxyl group-containing acrylic resin Styrene 300.0 parts Ethyl acrylate 210.0 methacrylic m
90.0 Benzoyl peroxide 1
2.0 A storm of the mixture with the above composition was placed in a 4-tube flask purged with nitrogen gas, heated to 80 to 90°C, kept at that temperature, and gradually added the remaining 38 drops over a period of 2 hours. After the addition was complete, After further stirring at that temperature for 2 hours, it was cooled, and the resulting mixture had an acid value of 93 (in terms of solid content, the same applies hereinafter), a solid content of 59.7%, and a viscosity of 4100 cps (25°C, all viscosities below are 25°C).
A carboxyl group-containing resin solution was obtained.
(B) エポキシ樹脂溶液の製造
エピコート1007 500 部窒素ガ
ス置換した4ツロフラスコに全量仕込み、徐々に加熱し
て内温を100°Cまで上げ、1時間攪拌完全に溶解し
た後80°Cまで冷却し、固形分60%のエポキシ樹脂
溶液を得た。(B) Manufacture of epoxy resin solution 500 parts of Epicote 1007 was charged into a 4-tube flask purged with nitrogen gas, gradually heated to raise the internal temperature to 100°C, stirred for 1 hour to completely dissolve, and then cooled to 80°C. An epoxy resin solution having a solid content of 60% was obtained.
(C)水性被覆用樹脂組成物の調製
■ 上記(A)カルボキシル基含有
アクリル系樹脂溶液 100.0部上記(B)
エポキシ樹脂溶液 50.0■ 2−ジメチルアミ
ノエタノール 9.3■ イオン交換水
290.74ツロフラスコに■を全量仕込み、攪拌
しなから■を添加して、含有カルボキシル基に対してほ
ぼ当モル中和を行なった後、内温を80°Cまで上昇さ
せ、この温度で30分間かきまぜを続けた後室温まで冷
却した。オキシラン%の減少率は63.5%であL、粘
度もクツキング前に比較してクツキング後は1.5倍に
増粘していた。(C) Preparation of aqueous coating resin composition 100.0 parts of the above (A) carboxyl group-containing acrylic resin solution (B) above
Epoxy resin solution 50.0■ 2-dimethylaminoethanol 9.3■ Ion exchange water
290.74 Charge the entire amount of ■ into a Tulo flask, add ■ without stirring, and neutralize the contained carboxyl groups approximately equimolarly, then raise the internal temperature to 80°C, and at this temperature After stirring for a minute, the mixture was cooled to room temperature. The reduction rate of oxirane % was 63.5% L, and the viscosity was also 1.5 times thicker after packing compared to before packing.
かくして得られた分散体に固形分と等量の吸油量20、
比重4.2であるルチル形酸化チタンおよびイオン交換
水を添加して樹脂と酸化チタンの合計の固形分が50%
となるように調製し、この混合物をボールミル形式のア
トライターによって混練することにより酸化チタンを均
一に分散させた。The thus obtained dispersion has an oil absorption of 20, which is equivalent to the solid content.
By adding rutile titanium oxide with a specific gravity of 4.2 and ion-exchanged water, the total solid content of resin and titanium oxide is 50%.
This mixture was kneaded using a ball mill type attritor to uniformly disperse titanium oxide.
次にこのチタンホワイト含有水性エポキシ−アクリル系
塗料を伸び縦2.0%、横6.0%1坪量300 g/
ra2で、化学パルプとして針葉樹パルプ(NBKP)
30wt%、広葉樹パルプ(LBKP) 70wt%
を使用し、無機填料としてタルクを5wt%含み、サイ
ズ剤としてアルキルケテンダイヤ−が使用された中性紙
の紙基質の両面にバーコーターで塗布し、190℃で1
分間オーブン中で乾燥焼付を行った。塗料の塗布量は片
面14g/m2 であL、隠蔽顔料の塗布量は7g7m
2 であった。Next, this titanium white-containing water-based epoxy-acrylic paint was stretched by 2.0% in length and 6.0% in width.1 basis weight: 300 g/
Softwood pulp (NBKP) as chemical pulp with RA2
30wt%, hardwood pulp (LBKP) 70wt%
It was coated with a bar coater on both sides of an acid-free paper substrate containing 5 wt% of talc as an inorganic filler and alkyl ketene diamond as a sizing agent.
A dry bake was carried out in the oven for a minute. The amount of paint applied is 14g/m2 on one side, and the amount of concealing pigment applied is 7g/m2.
It was 2.
かくして得られた積層体の断面を光学m微鏡を用いて拡
大撮影した写真を描いた図を第3図に示す、この図より
Lおよびlを測定したところ、Lは380μm、73は
最大値で21.7ALm、最少値で8.9 ALm、
”f’均値で10.3gmであった。従って24/Lの
値は最大イ1Nで0.057 、最少イffo、018
、乎均値で0.027であった。Figure 3 shows a photograph of the cross-section of the thus obtained laminate taken magnified using an optical microscope. When L and l were measured from this figure, L was 380 μm, and 73 was the maximum value. 21.7 ALm at minimum value, 8.9 ALm at minimum value,
The average value of ``f' was 10.3 gm. Therefore, the value of 24/L is 0.057 at maximum i1N, and 0.057 at minimum iffo, 018
, the average value was 0.027.
次に、このチタンホワイト含有エポキシ−アクリル系塗
料が両面に塗布された積層体を用い、ブランキング及び
罫線入れを行った後調温を行い140℃に保持されたプ
レス金型によってプレス成型することによL、第1図に
示すような縦16CI11.横8.5cm、深さ2cm
の角型トレーを得た。Next, using the laminate coated with this titanium white-containing epoxy-acrylic paint on both sides, blanking and scoring are performed, followed by temperature control and press molding using a press mold maintained at 140°C. L, vertical 16CI11. as shown in FIG. Width 8.5cm, depth 2cm
A square tray was obtained.
この場合、成形時に塗料が金型に付着したL、脱落した
りすることはなく、またクラックや割れも生じることな
く成形が満足に行えた。In this case, the paint adhered to the mold during molding and did not fall off, and the molding was performed satisfactorily without any cracks or cracks.
この角型トレーにチキンナゲツトを6個入れ、20間冷
凍庫内で保存後5オーブントースタ−で8分間加熱した
。加熱読了後オーブントースタ−からトレーを取り出し
、チキンナゲツトを賞味したところ適温であL、美味で
あった。また、この際角型トレーの表面は焦げず、変色
は見られなかった。Six chicken nuggets were placed in this square tray, stored in a freezer for 20 minutes, and then heated in a toaster oven for 8 minutes. After heating, I took the tray out of the toaster oven and tried the chicken nuggets, which were at the right temperature and delicious. Further, at this time, the surface of the square tray was not burnt and no discoloration was observed.
実施例2〜5.比較例1,2
実施例1で用いた紙基質の両面に第1表に示す塗料を塗
布量が片面当り固形分14g/m2になるようにバーコ
ーターで塗布し、190’Cで1分間オーブン中で乾燥
キュアーした。Examples 2-5. Comparative Examples 1 and 2 The paint shown in Table 1 was applied to both sides of the paper substrate used in Example 1 using a bar coater so that the coating amount was 14 g/m2 solids per side, and the mixture was baked in an oven at 190'C for 1 minute. It was dried and cured inside.
かくして得られた各種の積層体の断面を光学顕微鏡を用
いて拡大撮影した写真を描いた図を夫々第4図乃至第9
図に示す、この図よりLおよびiを3+11定し、f/
Lを計算した値を第1表に示す。Figures 4 to 9 depict photographs of the cross-sections of the various laminates obtained in this way, taken enlarged using an optical microscope.
From this figure, L and i are determined as 3+11, and f/
The calculated values of L are shown in Table 1.
次に各々の積層体を用い、ブランキング及び罫線入れを
行った後、140°Cに保持されたプレス金型により第
1図に示すような縦16cm、横9.5cm、深さ2.
0cmの角型トレーに成形した。この場合のプレス成形
性すなわち、金型への塗料付看、塗料の脱落、塗料のク
ラック、積層体の破断の程度を第1表に示す。第1表よ
り明らかなように有機溶媒系の塗料を使用した場合、A
/Lの値が大きくなL、成形時に破断したりクラックが
生じる傾向が認められた。Next, each laminate was blanked and ruled, and then molded with a press mold maintained at 140°C to form a size of 16 cm in length, 9.5 cm in width, and 2.5 cm in depth as shown in Figure 1.
It was molded into a 0 cm square tray. Table 1 shows the press formability in this case, that is, the degree of paint sticking to the mold, paint falling off, paint cracking, and laminate breakage. As is clear from Table 1, when organic solvent-based paint is used, A
When the value of /L was large, it was observed that there was a tendency for breakage or cracks to occur during molding.
第1図は1本発明の耐熱性紙容器を示す斜視図であL、
第2図は、本発明の紙容器の器壁部の断面構造図であL
、
第3図は実施例1の積層体の断面構造を示す顕微鏡写真
を描いた図であL、
第4図、第5図、第6図及び第7図は夫々実施例2乃至
5の積層体の断面構造を示す顕微鏡写真を描いた図であ
L、
第8図及び第9図は比較例1及び2の積層体の断面構造
を示す顕微鏡写真を描いた図である。
引照数字1は底壁部、2a、2b、2c及び2dは側壁
部、3はひだ部、4はフランジ部乃至カール部、10は
壁部、11は紙基質、12a。
12bは#熱性被覆層を示す。
第1図
第3図 第4図
第5図 第6図
第7図 第8図
第9図FIG. 1 is a perspective view showing a heat-resistant paper container of the present invention, and FIG. 2 is a cross-sectional structural view of the wall of the paper container of the present invention.
, FIG. 3 is a microscopic photograph showing the cross-sectional structure of the laminate of Example 1, and FIGS. 4, 5, 6, and 7 are the laminates of Examples 2 to 5, respectively. FIGS. 8 and 9 are micrographs showing the cross-sectional structures of the laminates of Comparative Examples 1 and 2. FIGS. Reference number 1 is the bottom wall, 2a, 2b, 2c, and 2d are the side walls, 3 is the fold, 4 is the flange or curl, 10 is the wall, 11 is the paper substrate, and 12a. 12b indicates #thermal coating layer. Figure 1 Figure 3 Figure 4 Figure 5 Figure 6 Figure 7 Figure 8 Figure 9
Claims (7)
れた樹脂コート層とから成る有底無継目成形容器におい
て、 樹脂コート層が熱硬化性樹脂と隠蔽顔料とを含有して成
り、該樹脂コート層は積層体の厚さをL、該コート層表
面から紙基質内への浸透深さをlとしたとき、l/L<
0.1を満足するように設けられていることを特徴とす
る有底無継目成形容器。(1) A bottomed seamless molded container consisting of a paper substrate and a resin coat layer provided on at least one surface of the paper substrate, in which the resin coat layer contains a thermosetting resin and a hiding pigment; For the resin coat layer, where L is the thickness of the laminate and l is the penetration depth from the surface of the coat layer into the paper substrate, l/L<
1. A seamless molded container with a bottom, characterized in that the container is provided so as to satisfy 0.1.
囲第1項記載の成形容器。(2) The molded container according to claim 1, wherein the paper substrate is low acid paper or neutral paper.
脂に対して反応性を有する硬化剤樹脂成分とを含む硬化
性組成物である特許請求の範囲第1項記載の成形容器。(3) The molded container according to claim 1, wherein the thermosetting resin is a curable composition containing an epoxy resin component and a curing agent resin component that is reactive with the epoxy resin.
1項記載の成形容器。(4) The molded container according to claim 1, wherein the hiding pigment is titanium dioxide.
.0μmの熱硬化性樹脂とを含む水性分散体を、紙基質
の少なくとも一方の表面に塗布し、塗布層を乾燥し、熱
硬化性樹脂を硬化させ、得られる積層体を有底無継目容
器形状にプレス成形することを特徴とする紙製有底無継
目成形容器の製法。(5) Hiding pigment as dispersoid and average particle size 0.05 to 1
.. An aqueous dispersion containing a 0 μm thermosetting resin is applied to at least one surface of the paper substrate, the applied layer is dried, the thermosetting resin is cured, and the resulting laminate is shaped into a seamless container with a bottom. A method for producing a bottomed, seamlessly molded paper container, which is characterized by press molding.
硬化性エポキシ−アクリル樹脂である特許請求の範囲第
5項記載の方法。(6) The method according to claim 5, wherein the aqueous dispersion of thermosetting resin is a curable epoxy-acrylic resin having self-emulsifying properties.
溶性型の熱硬化性エポキシ−アクリル系樹脂を含む水性
塗料を、紙基質の少なくとも一方の表面に塗布し、塗布
層を乾燥し、熱硬化性樹脂を硬化させ、得られる積層体
を有底無継目容器形状にプレス成形することを特徴とす
る紙製有底無継目成形容器の製法。(7) A water-based paint containing a hiding pigment as a dispersoid and a water-soluble thermosetting epoxy-acrylic resin as a resin component is applied to at least one surface of the paper substrate, the coated layer is dried, and then heated 1. A method for producing a seamless molded paper container with a bottom, which comprises curing a curable resin and press-molding the resulting laminate into the shape of a seamless container with a bottom.
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61223868A JPS6382936A (en) | 1986-09-24 | 1986-09-24 | Closed-end seamless molded vessel made of paper and manufacture thereof |
DE8787303680T DE3775265D1 (en) | 1986-04-28 | 1987-04-27 | CONTAINER MADE OF HEAT-RESISTANT PAPER AND METHOD FOR THE PRODUCTION THEREOF. |
CA 535592 CA1276895C (en) | 1986-04-28 | 1987-04-27 | Heat-resistant paper container and process for preparation thereof |
EP19870303680 EP0244179B1 (en) | 1986-04-28 | 1987-04-27 | Heat-resistant paper container and process for preparation thereof |
US07/043,655 US4775560A (en) | 1986-04-28 | 1987-04-28 | Heat-resistant paper container and process for preparation thereof |
KR870004097A KR870009645A (en) | 1986-04-28 | 1987-04-28 | Heat-resistant paper container and its manufacturing method |
US07/159,988 US5078939A (en) | 1986-04-28 | 1988-05-09 | Process for preparation of a heat resistance container |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61223868A JPS6382936A (en) | 1986-09-24 | 1986-09-24 | Closed-end seamless molded vessel made of paper and manufacture thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6382936A true JPS6382936A (en) | 1988-04-13 |
JPH0217422B2 JPH0217422B2 (en) | 1990-04-20 |
Family
ID=16804965
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61223868A Granted JPS6382936A (en) | 1986-04-28 | 1986-09-24 | Closed-end seamless molded vessel made of paper and manufacture thereof |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6382936A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001088819A (en) * | 1999-07-22 | 2001-04-03 | Dainippon Printing Co Ltd | Lid |
JP2003155018A (en) * | 2001-11-15 | 2003-05-27 | Toppan Printing Co Ltd | Draw molded paper container |
US9408745B2 (en) | 2007-08-21 | 2016-08-09 | Zeltiq Aesthetics, Inc. | Monitoring the cooling of subcutaneous lipid-rich cells, such as the cooling of adipose tissue |
US9655770B2 (en) | 2007-07-13 | 2017-05-23 | Zeltiq Aesthetics, Inc. | System for treating lipid-rich regions |
US9737434B2 (en) | 2008-12-17 | 2017-08-22 | Zeltiq Aestehtics, Inc. | Systems and methods with interrupt/resume capabilities for treating subcutaneous lipid-rich cells |
US9844461B2 (en) | 2010-01-25 | 2017-12-19 | Zeltiq Aesthetics, Inc. | Home-use applicators for non-invasively removing heat from subcutaneous lipid-rich cells via phase change coolants |
US9861520B2 (en) | 2009-04-30 | 2018-01-09 | Zeltiq Aesthetics, Inc. | Device, system and method of removing heat from subcutaneous lipid-rich cells |
US10092346B2 (en) | 2010-07-20 | 2018-10-09 | Zeltiq Aesthetics, Inc. | Combined modality treatment systems, methods and apparatus for body contouring applications |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5343209A (en) * | 1976-10-01 | 1978-04-19 | Nikkiso Co Ltd | Reciprocating pumps |
JPS573492A (en) * | 1980-06-06 | 1982-01-08 | Nec Corp | Selecting system of outgoing line |
JPS5741890A (en) * | 1980-08-25 | 1982-03-09 | Dengensha Mfg Co Ltd | Driving device for welding gun |
JPS587900U (en) * | 1981-07-07 | 1983-01-19 | 株式会社興人 | laminated paper |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS587900B2 (en) * | 1977-09-29 | 1983-02-12 | 三菱重工業株式会社 | indoor ventilation system |
-
1986
- 1986-09-24 JP JP61223868A patent/JPS6382936A/en active Granted
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5343209A (en) * | 1976-10-01 | 1978-04-19 | Nikkiso Co Ltd | Reciprocating pumps |
JPS573492A (en) * | 1980-06-06 | 1982-01-08 | Nec Corp | Selecting system of outgoing line |
JPS5741890A (en) * | 1980-08-25 | 1982-03-09 | Dengensha Mfg Co Ltd | Driving device for welding gun |
JPS587900U (en) * | 1981-07-07 | 1983-01-19 | 株式会社興人 | laminated paper |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001088819A (en) * | 1999-07-22 | 2001-04-03 | Dainippon Printing Co Ltd | Lid |
JP2003155018A (en) * | 2001-11-15 | 2003-05-27 | Toppan Printing Co Ltd | Draw molded paper container |
US9655770B2 (en) | 2007-07-13 | 2017-05-23 | Zeltiq Aesthetics, Inc. | System for treating lipid-rich regions |
US9408745B2 (en) | 2007-08-21 | 2016-08-09 | Zeltiq Aesthetics, Inc. | Monitoring the cooling of subcutaneous lipid-rich cells, such as the cooling of adipose tissue |
US9737434B2 (en) | 2008-12-17 | 2017-08-22 | Zeltiq Aestehtics, Inc. | Systems and methods with interrupt/resume capabilities for treating subcutaneous lipid-rich cells |
US9861520B2 (en) | 2009-04-30 | 2018-01-09 | Zeltiq Aesthetics, Inc. | Device, system and method of removing heat from subcutaneous lipid-rich cells |
US9844461B2 (en) | 2010-01-25 | 2017-12-19 | Zeltiq Aesthetics, Inc. | Home-use applicators for non-invasively removing heat from subcutaneous lipid-rich cells via phase change coolants |
US10092346B2 (en) | 2010-07-20 | 2018-10-09 | Zeltiq Aesthetics, Inc. | Combined modality treatment systems, methods and apparatus for body contouring applications |
Also Published As
Publication number | Publication date |
---|---|
JPH0217422B2 (en) | 1990-04-20 |
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