JPH04197300A - Bar code label and cloth with bar code label - Google Patents
Bar code label and cloth with bar code labelInfo
- Publication number
- JPH04197300A JPH04197300A JP2326628A JP32662890A JPH04197300A JP H04197300 A JPH04197300 A JP H04197300A JP 2326628 A JP2326628 A JP 2326628A JP 32662890 A JP32662890 A JP 32662890A JP H04197300 A JPH04197300 A JP H04197300A
- Authority
- JP
- Japan
- Prior art keywords
- resistant
- heat
- coating layer
- barcode
- heat resistant
- 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.)
- Pending
Links
- 239000004744 fabric Substances 0.000 title claims abstract description 16
- 239000011247 coating layer Substances 0.000 claims abstract description 43
- 239000002985 plastic film Substances 0.000 claims abstract description 30
- 229920006255 plastic film Polymers 0.000 claims abstract description 21
- 230000001070 adhesive effect Effects 0.000 claims description 20
- 239000000853 adhesive Substances 0.000 claims description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
- 239000003599 detergent Substances 0.000 claims description 11
- 229920003023 plastic Polymers 0.000 claims description 10
- -1 alkoxy silane Chemical compound 0.000 abstract description 20
- 239000010410 layer Substances 0.000 abstract description 18
- 229920000642 polymer Polymers 0.000 abstract description 16
- 229920005989 resin Polymers 0.000 abstract description 14
- 239000011347 resin Substances 0.000 abstract description 14
- 229920000728 polyester Polymers 0.000 abstract description 11
- 238000004140 cleaning Methods 0.000 abstract description 8
- 229920003235 aromatic polyamide Polymers 0.000 abstract description 6
- 125000005462 imide group Chemical group 0.000 abstract description 5
- 229920000193 polymethacrylate Polymers 0.000 abstract description 5
- XWUCFAJNVTZRLE-UHFFFAOYSA-N 7-thiabicyclo[2.2.1]hepta-1,3,5-triene Chemical compound C1=C(S2)C=CC2=C1 XWUCFAJNVTZRLE-UHFFFAOYSA-N 0.000 abstract description 4
- 229910000077 silane Inorganic materials 0.000 abstract 1
- 238000000034 method Methods 0.000 description 30
- 238000000576 coating method Methods 0.000 description 25
- 239000010408 film Substances 0.000 description 24
- 239000011248 coating agent Substances 0.000 description 20
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 11
- 229920001577 copolymer Polymers 0.000 description 11
- 239000000203 mixture Substances 0.000 description 11
- 239000000463 material Substances 0.000 description 8
- 238000009958 sewing Methods 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 239000012790 adhesive layer Substances 0.000 description 7
- 238000004132 cross linking Methods 0.000 description 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- 125000003118 aryl group Chemical group 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 239000000049 pigment Substances 0.000 description 6
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 5
- 239000004760 aramid Substances 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 239000003431 cross linking reagent Substances 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-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
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 4
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 4
- 238000007756 gravure coating Methods 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 4
- 239000000976 ink Substances 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 3
- 239000004677 Nylon Substances 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000002411 adverse Effects 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
- 238000003851 corona treatment Methods 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 238000003475 lamination Methods 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229920001778 nylon Polymers 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- 239000011342 resin composition Substances 0.000 description 3
- 238000004381 surface treatment Methods 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- KUDUQBURMYMBIJ-UHFFFAOYSA-N 2-prop-2-enoyloxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC(=O)C=C KUDUQBURMYMBIJ-UHFFFAOYSA-N 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-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
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 229920006243 acrylic copolymer Polymers 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
- 230000002950 deficient Effects 0.000 description 2
- 238000007607 die coating method Methods 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 239000001530 fumaric acid Substances 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000001023 inorganic pigment Substances 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- PQXKHYXIUOZZFA-UHFFFAOYSA-M lithium fluoride Chemical compound [Li+].[F-] PQXKHYXIUOZZFA-UHFFFAOYSA-M 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 229920001225 polyester resin Polymers 0.000 description 2
- 239000004645 polyester resin Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 229920003051 synthetic elastomer Polymers 0.000 description 2
- 239000005061 synthetic rubber Substances 0.000 description 2
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 229920001567 vinyl ester resin Polymers 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 description 1
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 1
- UTOVMEACOLCUCK-SNAWJCMRSA-N (e)-4-butoxy-4-oxobut-2-enoic acid Chemical compound CCCCOC(=O)\C=C\C(O)=O UTOVMEACOLCUCK-SNAWJCMRSA-N 0.000 description 1
- VTWGIDKXXZRLGH-CMDGGOBGSA-N (e)-4-octoxy-4-oxobut-2-enoic acid Chemical compound CCCCCCCCOC(=O)\C=C\C(O)=O VTWGIDKXXZRLGH-CMDGGOBGSA-N 0.000 description 1
- VTWGIDKXXZRLGH-HJWRWDBZSA-N (z)-4-octoxy-4-oxobut-2-enoic acid Chemical compound CCCCCCCCOC(=O)\C=C/C(O)=O VTWGIDKXXZRLGH-HJWRWDBZSA-N 0.000 description 1
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- WMRCTEPOPAZMMN-UHFFFAOYSA-N 2-undecylpropanedioic acid Chemical compound CCCCCCCCCCCC(C(O)=O)C(O)=O WMRCTEPOPAZMMN-UHFFFAOYSA-N 0.000 description 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 1
- LZMNXXQIQIHFGC-UHFFFAOYSA-N 3-[dimethoxy(methyl)silyl]propyl 2-methylprop-2-enoate Chemical compound CO[Si](C)(OC)CCCOC(=O)C(C)=C LZMNXXQIQIHFGC-UHFFFAOYSA-N 0.000 description 1
- GNSFRPWPOGYVLO-UHFFFAOYSA-N 3-hydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCO GNSFRPWPOGYVLO-UHFFFAOYSA-N 0.000 description 1
- QZPSOSOOLFHYRR-UHFFFAOYSA-N 3-hydroxypropyl prop-2-enoate Chemical compound OCCCOC(=O)C=C QZPSOSOOLFHYRR-UHFFFAOYSA-N 0.000 description 1
- XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 1
- SOHCOYTZIXDCCO-UHFFFAOYSA-N 6-thiabicyclo[3.1.1]hepta-1(7),2,4-triene Chemical group C=1C2=CC=CC=1S2 SOHCOYTZIXDCCO-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 241001385733 Aesculus indica Species 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-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
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000004962 Polyamide-imide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004734 Polyphenylene sulfide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- IDCBOTIENDVCBQ-UHFFFAOYSA-N TEPP Chemical compound CCOP(=O)(OCC)OP(=O)(OCC)OCC IDCBOTIENDVCBQ-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- FMRLDPWIRHBCCC-UHFFFAOYSA-L Zinc carbonate Chemical compound [Zn+2].[O-]C([O-])=O FMRLDPWIRHBCCC-UHFFFAOYSA-L 0.000 description 1
- 239000005083 Zinc sulfide Substances 0.000 description 1
- BWVAOONFBYYRHY-UHFFFAOYSA-N [4-(hydroxymethyl)phenyl]methanol Chemical compound OCC1=CC=C(CO)C=C1 BWVAOONFBYYRHY-UHFFFAOYSA-N 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 125000002947 alkylene group Chemical group 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
- 125000003368 amide group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 238000005282 brightening Methods 0.000 description 1
- INLLPKCGLOXCIV-UHFFFAOYSA-N bromoethene Chemical compound BrC=C INLLPKCGLOXCIV-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- UTOVMEACOLCUCK-PLNGDYQASA-N butyl maleate Chemical compound CCCCOC(=O)\C=C/C(O)=O UTOVMEACOLCUCK-PLNGDYQASA-N 0.000 description 1
- QHIWVLPBUQWDMQ-UHFFFAOYSA-N butyl prop-2-enoate;methyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C(C)=C.CCCCOC(=O)C=C QHIWVLPBUQWDMQ-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 1
- 229910001634 calcium fluoride Inorganic materials 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 150000001733 carboxylic acid esters Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000012790 confirmation Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 125000004386 diacrylate group Chemical group 0.000 description 1
- VVYDVQWJZWRVPE-UHFFFAOYSA-L dimethyltin(2+);diiodide Chemical compound C[Sn](C)(I)I VVYDVQWJZWRVPE-UHFFFAOYSA-L 0.000 description 1
- 238000005108 dry cleaning Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- AFSIMBWBBOJPJG-UHFFFAOYSA-N ethenyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC=C AFSIMBWBBOJPJG-UHFFFAOYSA-N 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- ZLNAFSPCNATQPQ-UHFFFAOYSA-N ethenyl-dimethoxy-methylsilane Chemical compound CO[Si](C)(OC)C=C ZLNAFSPCNATQPQ-UHFFFAOYSA-N 0.000 description 1
- NUFVQEIPPHHQCK-UHFFFAOYSA-N ethenyl-methoxy-dimethylsilane Chemical compound CO[Si](C)(C)C=C NUFVQEIPPHHQCK-UHFFFAOYSA-N 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- FKDLBUPSJQZYFZ-UHFFFAOYSA-N ethoxy-ethyl-dimethylsilane Chemical compound CCO[Si](C)(C)CC FKDLBUPSJQZYFZ-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000009501 film coating Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
- 125000005843 halogen group Chemical group 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
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910017053 inorganic salt Inorganic materials 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 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
- 238000007759 kiss coating Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 125000004674 methylcarbonyl group Chemical group CC(=O)* 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- KPRJPLYRJNQHJP-UHFFFAOYSA-N n-[butoxy(hydroxy)methyl]prop-2-enamide Chemical compound CCCCOC(O)NC(=O)C=C KPRJPLYRJNQHJP-UHFFFAOYSA-N 0.000 description 1
- RXOHFPCZGPKIRD-UHFFFAOYSA-N naphthalene-2,6-dicarboxylic acid Chemical compound C1=C(C(O)=O)C=CC2=CC(C(=O)O)=CC=C21 RXOHFPCZGPKIRD-UHFFFAOYSA-N 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- HVAMZGADVCBITI-UHFFFAOYSA-M pent-4-enoate Chemical compound [O-]C(=O)CCC=C HVAMZGADVCBITI-UHFFFAOYSA-M 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- 238000009832 plasma treatment Methods 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002312 polyamide-imide Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 1
- QTECDUFMBMSHKR-UHFFFAOYSA-N prop-2-enyl prop-2-enoate Chemical compound C=CCOC(=O)C=C QTECDUFMBMSHKR-UHFFFAOYSA-N 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000008054 sulfonate salts Chemical class 0.000 description 1
- 150000003457 sulfones Chemical group 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- 239000000271 synthetic detergent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000010345 tape casting Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- UKRDPEFKFJNXQM-UHFFFAOYSA-N vinylsilane Chemical class [SiH3]C=C UKRDPEFKFJNXQM-UHFFFAOYSA-N 0.000 description 1
- 239000012463 white pigment Substances 0.000 description 1
- 239000011667 zinc carbonate Substances 0.000 description 1
- 229910000010 zinc carbonate Inorganic materials 0.000 description 1
- 235000004416 zinc carbonate Nutrition 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、耐熱、耐水、耐洗濯性に優れた布帛製品に取
り付けるバーコードラベルに関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a barcode label attached to a fabric product having excellent heat resistance, water resistance, and washing resistance.
ホテル、病院、レストランなどにおいて大量に使用され
る衣料品、シーツ、タオル、お絞り等のクリーニングに
おいて、これらの布帛製品は製品種別、耐用年数、クリ
ーニンク′依頼主などが様々である。その管理の合理化
や省力化法として各布帛製品にバーコードラベルを付す
ることか望まれている。When cleaning clothing, sheets, towels, diaphragms, etc. that are used in large quantities in hotels, hospitals, restaurants, etc., these fabric products vary in product type, service life, and cleaning clients. It is desired to attach a barcode label to each fabric product as a method to streamline management and save labor.
布帛製品に識別用タグを付する方法としては、例えば、
特公平2−235976号公報が知られている。Examples of methods for attaching identification tags to fabric products include:
Japanese Patent Publication No. 2-235976 is known.
しかし、前述の特公平2−235976号公報は、ドラ
イクリーニング用であり、またクリーニング毎にタグを
いちいち取り付ける必要がある。However, the above-mentioned Japanese Patent Publication No. 2-235976 is for dry cleaning, and it is necessary to attach a tag each time cleaning is performed.
したがって、本発明は、これら従来技術の欠点を解消せ
しめ、クリーニング相当回数繰り返しても、ラベルの剥
れ、破断、熱収縮、印字の不鮮明化などか生じない、安
価で有用な布帛製品用バーコードラベルを提供するもの
である。Therefore, the present invention solves the drawbacks of these conventional techniques, and provides an inexpensive and useful barcode for fabric products that does not cause label peeling, breakage, heat shrinkage, or blurred printing even after repeated cleaning a considerable number of times. It provides a label.
〔課題を解決するための手段]
本発明は、耐熱性プラスチックフィルムの片面に耐熱性
被覆層を塗設し、該耐熱性被覆層に耐熱性インクを用い
てバーコードを印字したことを特徴とするバーコードラ
ベル、を要旨とする。[Means for Solving the Problems] The present invention is characterized in that a heat-resistant coating layer is coated on one side of a heat-resistant plastic film, and a barcode is printed on the heat-resistant coating layer using heat-resistant ink. The gist is the barcode label.
本発明の耐熱性プラスチックフィルムおよび耐熱性透明
プラスチックフィルムとしては、フッ素樹脂、ポリ−ル
ーフユニレンスルフィドを主成分とする樹脂組成物、分
子鎖中にイミド基を有する重合体、芳香族ポリアミド系
重合体のいずれかからなるフィルムであって、これらの
フィルムの耐熱温度は150℃、望ましくは200’C
,より望ましくは240°C以上であり、また150℃
における熱収縮率は、2%以下が好ましく、さらに好ま
しくは250℃における熱収縮率が15%以下、より好
ましくは8%以下が望ましい。熱収縮率がこれを越える
と、耐熱性が劣り好ましくない。The heat-resistant plastic film and heat-resistant transparent plastic film of the present invention include a fluororesin, a resin composition containing poly-roof unilene sulfide as a main component, a polymer having an imide group in its molecular chain, an aromatic polyamide-based polymer, etc. These films have a heat resistance temperature of 150°C, preferably 200'C.
, more preferably 240°C or higher, and 150°C
The heat shrinkage rate at 250°C is preferably 2% or less, more preferably 15% or less at 250°C, and more preferably 8% or less. If the heat shrinkage rate exceeds this range, the heat resistance will be poor, which is not preferable.
また割れや破れの生じないようなしなやかさも必要であ
る。It also needs to be flexible enough to avoid cracking or tearing.
本発明におけるフッ素樹脂はポリテトラフルオロエチレ
ン・パーフルオロアルキルビニルエーテル共重合体(P
FA)やポリテトラフルオロエチレン−ポリへキサフル
オロプロピレン共重合体(F E P)等があげられる
。The fluororesin used in the present invention is polytetrafluoroethylene/perfluoroalkyl vinyl ether copolymer (P
FA) and polytetrafluoroethylene-polyhexafluoropropylene copolymer (FEP).
本発明におけるポリ−p−フェニレンスルフィドを主成
分とする樹脂組成物の構造は繰り返し単位((D−s
+を主たる構成単位とするポリフェニレンスルフィドで
ある。好ましくは本構成単位が70モル%以上であるこ
とがよく、さらに好ましくは90モル%以上であること
が望ましい。The structure of the resin composition containing poly-p-phenylene sulfide as a main component in the present invention is a repeating unit ((D-s
It is a polyphenylene sulfide whose main structural unit is +. Preferably, the content of this structural unit is 70 mol% or more, more preferably 90 mol% or more.
上記ポリマにおける繰り返し単位の残りの30モル%未
満については、
メタフェニレンスルフィドユニット羊。お−8)エーテ
ルユニット子(D−0−Cンモ。The remaining less than 30 mol% of repeating units in the above polymer are metaphenylene sulfide units. O-8) Ether unit child (D-0-C nmo).
スルホンユニット子(D−3O□−C叉チ。Sulfone unit (D-3O□-C cross.
ビフェニルユニッ)玉に臣ト(ラーS+。Biphenyl unit) Tama ni Omit (Ra S+.
ナフチルユニット±〔蓬陣汗汁。Naphthyl unit ± [Hougin sweat juice.
ここで、Rは炭素数1〜10のアルキル基、ニトロ基、
フェニル基、またはアルコキシ基である)などから構成
することかできる。Here, R is an alkyl group having 1 to 10 carbon atoms, a nitro group,
phenyl group or alkoxy group).
この発明におけるポリ−p−フェニレンスルフィドの特
性溶融粘度は、温度300℃、見掛けせん断速度200
sec−1の条件下で、500〜12000ポイズか好
ましく、700〜7000ポイズの範囲にあることが、
フィルムの製膜性、表面特性などの点からより好ましい
。The characteristic melt viscosity of poly-p-phenylene sulfide in this invention is at a temperature of 300°C and an apparent shear rate of 200°C.
Under the condition of sec-1, it is preferably 500 to 12,000 poise, and preferably in the range of 700 to 7,000 poise.
This is more preferred from the viewpoint of film formability, surface properties, etc.
本発明における分子鎖中にイミド基を有する重合体とは
、一般にポリイミド、ポリアミドイミドとして知られた
ものが有効に使用される。繰り返し単位を示すと下記の
ようなものがあげられる。As the polymer having an imide group in its molecular chain in the present invention, those generally known as polyimide and polyamideimide are effectively used. The following are examples of repeating units:
O CO \ / I ここで Ar、:4価の芳香族基 Ar2 :2価の芳香族基 Ar3 :3価の芳香族基 Ar4 :2価の芳香族基 をそれぞれ表わす。O C.O. \ / I here Ar,: tetravalent aromatic group Ar2: divalent aromatic group Ar3: trivalent aromatic group Ar4: divalent aromatic group respectively.
かかるAr、としては Ar2としては、 Ar3としては、 Ar4としては、 などが好ましい。As such Ar, As Ar2, As Ar3, As Ar4, etc. are preferable.
ここで、x=o、co、s、so、so2゜Y=O,C
o、S、So、SO2゜
OR,R10
z=o、co、s、so2゜
R,=アルキル(炭素原子数1〜6)。Here, x=o, co, s, so, so2゜Y=O, C
o, S, So, SO2°OR, R10 z=o, co, s, so2°R, = alkyl (1 to 6 carbon atoms).
あるいはこれらの芳香族環の水素原子の少なくとも1個
かアルキル基(炭素原子数か1〜6)、ヒドロキシル基
、ハロゲン基で置換されていてもよい。Alternatively, at least one hydrogen atom of these aromatic rings may be substituted with an alkyl group (having 1 to 6 carbon atoms), a hydroxyl group, or a halogen group.
本発明における分子鎖中にイミド基を有する重合体は他
の構成単位を含んだ共重合体であったり、他の成分との
ブレンド物であってもよいが、全重量中の40重量%以
上か前記一般式(A)または(B)の単位であることが
本発明に対して有効である。上記単位か40重量%未満
であると、フィルムとしての機械的強度、寸法安定性、
耐熱性などが損われるので好ましくない。The polymer having an imide group in its molecular chain in the present invention may be a copolymer containing other structural units or a blend with other components, but it may be at least 40% by weight of the total weight. It is effective for the present invention that it is a unit of the above general formula (A) or (B). If the above units are less than 40% by weight, the mechanical strength and dimensional stability of the film will be reduced.
It is not preferable because heat resistance etc. are impaired.
本発明における芳香族ポリアミド系重合体とは、下記一
般式
ただし、nは整数、R,、R,は
(ここでa、b、cはR,、R2とも同時にa=b=c
=Ol:なる、mとはな(、またa=o、b=c−1ま
たはc=o、a=b=1にならなし)よ−C)−、=C
H2−、−3O2−から選ばれるものである)
べ軍Hx旨→唖房。The aromatic polyamide polymer in the present invention has the following general formula, where n is an integer, and R, R, (where a, b, and c are R, R2 and a=b=c
=Ol: Naru, what is m (also, a=o, b=c-1 or c=o, a=b=1) -C) -, =C
(selected from H2-, -3O2-).
(ここでd、 eはd=e=1またはd=e=0ある
いはd=0.e=1になるように選ばれたOまt二は1
を表わし、Xは−C,,−〇−。(Here, d and e are selected so that d=e=1 or d=e=0 or d=0.e=1.
, and X is -C,, -〇-.
−CH2−+−5o2−から選ばれるものである)で示
される重合体において、該重合体を構成する全結合数の
うち少なくとも50%以上、さらに好ましくは70%以
上はパラ結合からなり、該重合体を構成するフェニル核
の少なくとも15%以上はアミド結合に対しオルトの位
置にノ10ゲン基(CI、Br、Fのうちから選はれる
もの)、またはニトロ基あるいはC1〜C3のアルキル
基、01〜C3のアルコキシ基などの置換基を有する芳
香族ポリアミドである。-CH2-+-5o2-), at least 50% or more, more preferably 70% or more of the total number of bonds constituting the polymer consists of para bonds, and At least 15% or more of the phenyl nuclei constituting the polymer contain a nitrogen group (selected from CI, Br, F), a nitro group, or a C1-C3 alkyl group at the position ortho to the amide bond. , is an aromatic polyamide having a substituent such as an alkoxy group of 01 to C3.
本発明の芳香族ポリアミド系重合体は上記のように全結
合数中の50%以上をパラ結合とするものであるか、全
結合中に、フィルムの可撓性、耐久性および強靭性を増
すため、50%未満の範囲でメタ、オルト、アルキレン
、エステル、複素環、尿素、ウレタン等の結合を含ませ
ることは好ましい。また本発明に言うオルト位置とは下
記の4つの位置のすべてを含むものである。As mentioned above, the aromatic polyamide polymer of the present invention has 50% or more of the total number of bonds as para bonds, or increases the flexibility, durability, and toughness of the film during the total number of bonds. Therefore, it is preferable to include bonds of meta, ortho, alkylene, ester, heterocycle, urea, urethane, etc. in a range of less than 50%. Further, the ortho position referred to in the present invention includes all of the following four positions.
ここでX1〜X4は本発明で言うオルトの位置を示すも
のである。具体例としては、一般式の中でa=1.b=
c=0でありCI基をもつなどがあるが下式のものは含
まれない。Here, X1 to X4 indicate ortho positions in the present invention. As a specific example, in the general formula, a=1. b=
There are examples in which c=0 and a CI group, but those of the following formula are not included.
しかし
のようなヒドラジド結合を有するポリマー、またのよう
なオキサイド結合を有するポリマーは含まれるものであ
る。However, polymers having hydrazide bonds, such as , and polymers having oxide bonds, such as , are included.
これらの重合体からフィルムを作るには一般に溶融製膜
は不可能であり、溶液状態からの乾式、湿式、乾湿式プ
ロセスによって製膜される。製膜用の溶液としては濃硫
酸やアミド系のN−メチルピロリドン、ジメチルアセト
アミド、ヘキサメチルホスホルアミドまたはこれと無機
塩との混合溶媒などを使用して調整される。To make films from these polymers, melt casting is generally not possible, and films are formed by dry, wet, or dry-wet processes from a solution state. The membrane-forming solution is prepared using concentrated sulfuric acid, amide-based N-methylpyrrolidone, dimethylacetamide, hexamethylphosphoramide, or a mixed solvent of these and an inorganic salt.
本発明の耐熱性被覆層とは、ポリ(メタ)アクリル酸エ
ステル共重合体を主成分とする組成物からなる層、また
はアルコキシシランもしくはグリシジル基を含有する不
飽和結合を有する化合物をグラフト化した非水系ポリエ
ステル共重合体を主成分とする組成物からなる層である
。The heat-resistant coating layer of the present invention is a layer made of a composition mainly composed of a poly(meth)acrylate copolymer, or a layer grafted with a compound having an unsaturated bond containing an alkoxysilane or a glycidyl group. This layer is made of a composition whose main component is a non-aqueous polyester copolymer.
本発明におけるポリ(メタ)アクリル酸エステル共重合
体を主成分とする組成物からなる層とは、そのものが耐
熱性被覆層中50重量%以上、好ましくは60重量%以
上であるものを指し、適宜他の物質を添加してもよい。In the present invention, the layer consisting of a composition mainly composed of a poly(meth)acrylic acid ester copolymer refers to one in which the composition itself accounts for 50% by weight or more, preferably 60% by weight or more in the heat-resistant coating layer. Other substances may be added as appropriate.
添加する樹脂は特に限定されないが、代表例としては、
ウレタン系樹脂、ポリエステル樹脂、ビニル系樹脂、ス
チレン系樹脂等の各種樹脂を挙げることが可能である。The resin to be added is not particularly limited, but representative examples include:
Examples include various resins such as urethane resin, polyester resin, vinyl resin, and styrene resin.
本発明でいうポリ(メタ)アクリル酸エステル共重合体
とは、反応性モノマを含有するポリ(メタ)アクリル酸
エステル共重合体である。かかる反応性モノマとしては
、官能基として、例えば、カルボキシル基(例えは、(
メタ)アクリル酸など)、水酸基((メタ)アクリル酸
2−ヒドロキシエチルなど)、アミド基((メタ)アク
リル酸アミドなど)、グリシジル基((メタ)アクリル
酸グリシジル基など)、アミノ基((メタ)アクリル酸
2−ジエチルアミノエチルなど)等を含有する化合物等
が挙げられる。The poly(meth)acrylic ester copolymer referred to in the present invention is a poly(meth)acrylic ester copolymer containing a reactive monomer. Such reactive monomers include functional groups such as carboxyl groups (for example, (
(meth)acrylic acid, etc.), hydroxyl group ((meth)acrylic acid 2-hydroxyethyl etc.), amide group ((meth)acrylic acid amide, etc.), glycidyl group ((meth)acrylic acid glycidyl group, etc.), amino group (( Examples include compounds containing 2-diethylaminoethyl meth)acrylate, etc.
本発明のポリ(メタ)アクリル酸エステル共重合体のT
g(カラス転移温度)について次式、[式中WA、
、 wA2、−WA−1? 、 WB、 、
WB2 、 ”’wb。T of the poly(meth)acrylic acid ester copolymer of the present invention
Regarding g (glass transition temperature), the following formula, [where WA,
, wA2, -WA-1? , WB, ,
WB2, ”'wb.
は、ポリ(メタ)アクリル酸エステル(A) 、 (
B)の重量分率を示し、Tg A+ 、 Tg A2
、・・・、TgAη、 Tg Ill、 Tg B
2・・・、 Tg B17は、ポリ (メタ)アクリ
ル酸エステル(A) 、 (lli のTgを絶対温
度で示したものである]の方法で計算したT値か30〜
100℃、より好ましくは40〜90°Cであることか
望ましい。この範囲より低いとプロツキンク性、耐熱性
か悪く、一方高いと密着性が悪くなり好ましくない。is poly(meth)acrylic ester (A), (
B) shows the weight fraction of Tg A+, Tg A2
,..., TgAη, Tg Ill, Tg B
2..., Tg B17 is the T value calculated by the method of poly(meth)acrylic acid ester (A), (Tg of lli expressed in absolute temperature), or 30~
It is desirable that the temperature is 100°C, more preferably 40 to 90°C. If it is lower than this range, the stickiness and heat resistance will be poor, while if it is higher than this range, the adhesion will be poor, which is not preferable.
本発明におけるポリ(メタ)アクリル酸エステル共重合
体を主成分とする組成物からなる層とは、そのものが耐
熱性被覆層中50重量%以上、好ましくは60重量%以
上、より好ましくは70重量%以上であるものを指し、
適宜他の物質を添加してもよい。添加する樹脂は特に限
定されないが、代表例としては、ウレタン系樹脂、ポリ
エステル樹脂、アクリル樹脂、ビニル系樹脂、スチレン
系樹脂等の各種樹脂を挙げることか可能である。In the present invention, the layer consisting of a composition mainly composed of a poly(meth)acrylic acid ester copolymer means that the layer itself is 50% by weight or more, preferably 60% by weight or more, and more preferably 70% by weight in the heat-resistant coating layer. % or more,
Other substances may be added as appropriate. The resin to be added is not particularly limited, but typical examples include various resins such as urethane resins, polyester resins, acrylic resins, vinyl resins, and styrene resins.
本発明においては、かかる耐熱性被覆層を前記耐熱性プ
ラスチックフィルムの少なくとも片面に設けるのである
かこの中で両面に設ける場合は、以下に述べる該耐熱性
被覆層の説明は少なくとも一方に適用されるものである
。In the present invention, the heat-resistant coating layer is provided on at least one side of the heat-resistant plastic film, or if it is provided on both sides, the following description of the heat-resistant coating layer applies to at least one side. It is something.
本発明でいう非水系ポリエステル共重合体とは、分子中
に親水性基或いは親水性成分、例えは、水酸基、カルボ
キシル基、カルボニル基、シアノ基、アミン基、メチル
カルボニル基、ポリエチレンクリコール、カルボン酸塩
、リン酸エステル塩、第四級アンモニウム塩、硫酸エス
テル塩、スルホン酸塩等が導入されていないポリエステ
ル共重合体であって、水不溶解性で、有機溶剤に均一に
溶解するものを意味する。但し、ポリエステル共重合体
の両末端が水酸基もしくはカルボキシル基であってもよ
い、
前記のポリエステル共重合体としては、ジカルボン酸成
分とグリコール成分を重縮合して得られるもので特に限
定するものではない。The non-aqueous polyester copolymer referred to in the present invention refers to a hydrophilic group or a hydrophilic component in the molecule, such as a hydroxyl group, a carboxyl group, a carbonyl group, a cyano group, an amine group, a methylcarbonyl group, a polyethylene glycol, or a carbonyl group. Polyester copolymers that do not contain acid salts, phosphate ester salts, quaternary ammonium salts, sulfate ester salts, sulfonate salts, etc., are insoluble in water and uniformly soluble in organic solvents. means. However, both ends of the polyester copolymer may be a hydroxyl group or a carboxyl group.The polyester copolymer mentioned above is not particularly limited as it can be obtained by polycondensing a dicarboxylic acid component and a glycol component. .
ジカルボン酸成分としては芳香族、脂肪族、脂環族のジ
カルボン酸であり例えばテレフタル酸、イソフタル酸、
オルソフタル酸、2,6−ナフタレンジカルボン酸、ア
ジピン酸、セバシン酸、コハク酸、グルタル酸、1.3
−シクロペンタンジカルボン酸、■、3−シクロヘキサ
ンジカルボン酸、ドデカンジカルボン酸、アゼライン酸
およびそれらのエステル形成性誘導体等を挙げることか
できる。The dicarboxylic acid component includes aromatic, aliphatic, and alicyclic dicarboxylic acids, such as terephthalic acid, isophthalic acid,
Orthophthalic acid, 2,6-naphthalene dicarboxylic acid, adipic acid, sebacic acid, succinic acid, glutaric acid, 1.3
Examples include -cyclopentanedicarboxylic acid, (1), 3-cyclohexanedicarboxylic acid, dodecanedicarboxylic acid, azelaic acid, and ester-forming derivatives thereof.
前述のジカルボン酸と反応させるクリコール成分として
は炭素数2〜8の脂肪族クリコール、又は炭素数6〜1
2の脂環族グリコールてあり、具体例としてはエチレン
グリコール、1,2−プロピレングリコール、]、]3
−プロパンジオール1.4−ブタンジオール、ネオペン
チルグリコール、1,6−ヘキサンジオール、1,2−
シクロヘキサンジメタツール、1,3−シクロヘキサン
ジメタツール、1,4−シクロヘキサンジメタツール、
p−キシリレンクリコール、ジエチレンクリコール、ト
リエチレンクリコールなとである。The glycol component to be reacted with the dicarboxylic acid mentioned above is an aliphatic glycol having 2 to 8 carbon atoms, or an aliphatic glycol having 6 to 1 carbon atoms.
2 alicyclic glycols, specific examples are ethylene glycol, 1,2-propylene glycol, ], ]3
-Propanediol 1,4-butanediol, neopentyl glycol, 1,6-hexanediol, 1,2-
Cyclohexane dimetatool, 1,3-cyclohexane dimetatool, 1,4-cyclohexane dimetatool,
These include p-xylylene glycol, diethylene glycol, and triethylene glycol.
これらの共重合ポリエステルは一般に直鎖状であること
か好ましく、反応性基を含有しないものが望ましい。ま
た共重合ポリエステルのカラス転位点は10〜90°C
1好ましくは40〜70°Cである場合、好適な耐ステ
ィック性を示す。These copolymerized polyesters are generally preferably linear, and preferably contain no reactive groups. In addition, the crow transition point of copolymerized polyester is 10 to 90°C.
1. Suitable stick resistance is exhibited when the temperature is preferably 40 to 70°C.
本発明でいう不飽和結合を有する化合物とは、非水系ポ
リエステル共重合体にグラフト化する化合物であり、具
体的には、ビニルエステル類として、例えば、プロピオ
ン酸ビニル、ステアリン酸ビニル、高級第3級ビニルエ
ステル、塩化ビニル、臭化ビニル、又不飽和カルボン酸
エステル類として、例えば、アクリル酸メチル、アクリ
ル酸エチル、アクリル酸ブチル、アクリル酸2エチルヘ
キシル、メタクリル酸メチル、メタクリル酸ブチル、マ
レイン酸ブチル、マレイン酸オクチル、フマル酸ブチル
、フマル酸オクチル、アクリル酸グリシジル、メタクリ
ル酸グリシジル、メタクリル酸ヒドロキシエチル、アク
リル酸ヒドロキシエチル、メタクリル酸ヒドロキシプロ
ピル、アクリル酸ヒドロキシプロピル、メタクリル酸ジ
メチルアミノエチル、アクリル酸ジメチルアミノエチル
、エチレングリコールジメタクリル酸エステル、エチレ
ンク゛リコールジアクリル酸エステル、ポリエチレング
リコールジメタクリル酸エステル、ポリエチレングリコ
ールジアクリル酸エステル、不飽和カルボン酸アミド類
として、例えばアクリルアミド、メタクリルアミド、メ
チロールアクリルアミド、ブトキシメチロールアクリル
アミド、不飽和ニトリル類として、例えはアクリロニト
リル、不飽和カルボン酸類として、例えばアクリル酸、
メタクリル酸、マレイン酸、フマル酸、イタコン酸、マ
イレン酸酸性エステル、フマル酸酸性エステル、イタコ
ン酸酸性エステル、アクリル化合物として、例えば酢酸
アリル、アリルク゛リシジルエーテル、メタクリル酸ア
リル、アクリル酸アリル、イタコン酸ジアリル、含窒素
化合物として、ビニルピリジン、ビニルイミタゾール、
炭化水素類として、例えはエチレン、プロピレン、ヘキ
セン、オクテン、スチレン、ビニルトルエン、ブタジェ
ン、ビニルシラン化合物として、例えばジメチルビニル
メトキシシラン、ジメチルエチルエトキシシラン、メチ
ルビニルジメトキシシラン、メチルビニルジェトキシシ
ラン、γ−メタクリロキシプロピルトリメトキシシラン
、γ−メタクリロキシプロピルメチルジメトキシシラン
などが挙げられ、これらの中から選ばれた少なくとも1
種以上か適用されるか特に限定されるものではない。The compound having an unsaturated bond as used in the present invention refers to a compound that is grafted onto a nonaqueous polyester copolymer. Specifically, vinyl esters such as vinyl propionate, vinyl stearate, and higher vinyl ester, vinyl chloride, vinyl bromide, unsaturated carboxylic acid esters such as methyl acrylate, ethyl acrylate, butyl acrylate, 2-ethylhexyl acrylate, methyl methacrylate, butyl methacrylate, butyl maleate. , octyl maleate, butyl fumarate, octyl fumarate, glycidyl acrylate, glycidyl methacrylate, hydroxyethyl methacrylate, hydroxyethyl acrylate, hydroxypropyl methacrylate, hydroxypropyl acrylate, dimethylaminoethyl methacrylate, dimethyl acrylate Aminoethyl, ethylene glycol dimethacrylate, ethylene glycol diacrylate, polyethylene glycol dimethacrylate, polyethylene glycol diacrylate, unsaturated carboxylic acid amides such as acrylamide, methacrylamide, methylol acrylamide, butoxymethylol Acrylamide, unsaturated nitriles such as acrylonitrile, unsaturated carboxylic acids such as acrylic acid,
Methacrylic acid, maleic acid, fumaric acid, itaconic acid, maleic acid ester, fumaric acid ester, itaconic acid ester, acrylic compounds such as allyl acetate, allyl cricidyl ether, allyl methacrylate, allyl acrylate, diallyl itaconate , as nitrogen-containing compounds, vinylpyridine, vinylimitazole,
Examples of hydrocarbons include ethylene, propylene, hexene, octene, styrene, vinyltoluene, butadiene, and vinylsilane compounds such as dimethylvinylmethoxysilane, dimethylethylethoxysilane, methylvinyldimethoxysilane, methylvinyljethoxysilane, γ- Examples include methacryloxypropyltrimethoxysilane, γ-methacryloxypropylmethyldimethoxysilane, and at least one selected from these.
There is no particular limitation as to whether it is applicable to more than one species or not.
グラフトは公知の反応によって行なえ、得られたグラフ
ト化共重合体は主鎖がポリエステル共重合体のため、基
材の耐熱性プラスチックフィルムと親和性に優れている
ので耐熱性被覆層はフィルム上により強固に形成できる
。更に、グラフト化合物が種々のインクと親和性が良い
ため、−層、印刷適性を高めることができる。Grafting can be carried out by a known reaction, and since the main chain of the resulting grafted copolymer is a polyester copolymer, it has excellent affinity with the heat-resistant plastic film of the base material, so the heat-resistant coating layer can be placed on the film. Can be formed strongly. Furthermore, since the graft compound has good affinity with various inks, it is possible to improve the printability of the layer.
本発明では、バーコードを印字した時、該シートが透明
では印刷の解像度や鮮明さ、印刷場所の確認等に支障を
生じるような場合、耐熱性被覆層に白色隠ペイ顔料を含
有せしめるこ吉か好ましい本発明でいう白色隠ペイ顔料
とは、耐熱性被覆層を白色に呈する無機あるいは有機顔
料であって、無機顔料としては、例えは、炭酸亜鉛、酸
化亜鉛、硫化亜鉛、タルク、カオリン、重質・軽質ある
いは合成の炭酸カルシウム、酸化チタン、シリカ、フッ
化リチウム、フッ化カルシウム、硫酸バリウム、アルミ
ナ、ジルコニア、リン酸カルシウム、天然あるいは合成
の膨潤性あるいは非膨潤性のマイカ等が挙げられ、有機
顔料としては、例えば、ポリスチレン、ポリメチルスチ
レン、ポリメトキシスチレン、ポリ塩化ビニル、ポリエ
チレン、ポリプロピレン、ポリ塩化ビニリデン、ポリメ
タクリレート、ポリメチルメタクリレート、ポリクロル
アクリレート等が挙げられ、これらの中から選ばれた少
なくとも1種以上が適用されるか、特に限定されるもの
ではない。また顔料は中空多孔質あるいは非中空多孔質
状態であってもよい。In the present invention, when a barcode is printed on a transparent sheet, if the sheet is transparent, it will be difficult to confirm the resolution and clarity of the print, and the confirmation of the printing location. The preferred white hidden pigment in the present invention is an inorganic or organic pigment that makes the heat-resistant coating layer appear white. Examples of the inorganic pigment include zinc carbonate, zinc oxide, zinc sulfide, talc, kaolin, Heavy, light or synthetic calcium carbonate, titanium oxide, silica, lithium fluoride, calcium fluoride, barium sulfate, alumina, zirconia, calcium phosphate, natural or synthetic swellable or non-swellable mica, etc. Examples of the pigment include polystyrene, polymethylstyrene, polymethoxystyrene, polyvinyl chloride, polyethylene, polypropylene, polyvinylidene chloride, polymethacrylate, polymethylmethacrylate, polychloroacrylate, etc. At least one or more types may be applied, but there is no particular limitation. Further, the pigment may be in a hollow porous state or a non-hollow porous state.
さらに前記顔料は、樹脂に対する分散性を良化するため
表面にグリシジル基、メチロール基等の官能基を付加さ
せるなどの処理が施されていてもよい。Furthermore, the pigment may be subjected to a treatment such as adding a functional group such as a glycidyl group or a methylol group to the surface in order to improve its dispersibility in a resin.
白色隠ペイ顔料を含む耐熱性被覆層のハンター白色度は
40%以上か好ましい。ハンター白色度が40%未満て
あれば隠ペイ性か不十分となり、例えばバーコードの場
合読み取りミスを生じる場合があり好ましくない。The Hunter whiteness of the heat-resistant coating layer containing a white hidden pigment is preferably 40% or more. If the Hunter whiteness is less than 40%, the concealment property will be insufficient and, for example, in the case of a bar code, reading errors may occur, which is not preferable.
また白色顔料の添加量は、0.1〜70重量%が好まし
く、5〜50重量%がより好ましい。添加量か0.1重
量%未満では白色隠ペイ性が不十分となり、70重量%
以上では耐熱性被覆層と基材の密着性が低下し易い。Further, the amount of white pigment added is preferably 0.1 to 70% by weight, more preferably 5 to 50% by weight. If the amount added is less than 0.1% by weight, the white hiding property will be insufficient, and 70% by weight.
Above this level, the adhesion between the heat-resistant coating layer and the base material tends to decrease.
本発明では、耐熱性被覆層の密着性、耐水性、耐薬品性
、耐熱性等をより良化せしめるため耐熱性被覆層に架橋
結合剤を含有させることが好ましい。In the present invention, it is preferred that the heat-resistant coating layer contain a crosslinking agent in order to further improve the adhesion, water resistance, chemical resistance, heat resistance, etc. of the heat-resistant coating layer.
本発明でいう架橋結合剤とは、前記の反応性モノマと架
橋反応し、最終的には三次元網状構造を有する耐熱性被
覆層とするための架橋剤であれば特に限定しないが、代
表例としては、アミン樹脂、エポキシ樹脂、メラミン樹
脂、イソシアナート類などから適宜選択される。さらに
架橋促進剤などの添加剤を加えてもよい。The crosslinking agent used in the present invention is not particularly limited as long as it is a crosslinking agent that undergoes a crosslinking reaction with the above-mentioned reactive monomer and ultimately forms a heat-resistant coating layer having a three-dimensional network structure, but typical examples include: The resin is appropriately selected from amine resins, epoxy resins, melamine resins, isocyanates, and the like. Furthermore, additives such as crosslinking accelerators may be added.
架橋促進剤は単独、場合によっては2種以上併用しても
よい。添加する架橋結合剤の量は架橋剤の種類によって
適宜選択されるが通常は反応性モノマを含有するポリ(
メタ)アクリル酸エステル共重合体の固型分100重量
部に対して、0.01〜50重量部が好ましく、0.1
〜30重量部がより好ましい。添加量が0.01重量部
未満ては架橋効果が低く、50重量部を越えるものは耐
熱性被覆層の密着性か低下したり、さらには塗布性が悪
化し均一層を形成し難い。また架橋促進剤としては、塩
類、無機物質、有機物質、酸物質、アルカリ物質など公
知のものを用いることかできる。添加する架橋促進剤の
量は、反応性モノマを含有するポリ(メタ)アクリル酸
エステル共重合体の固型分100重量部に対して、0.
001〜10重量部、好ましくは0.1〜5重量部であ
る。架橋結合剤を加えた反応性モノマを含有するポリ(
メタ)アクリル酸エステル共重合体は基材に塗布後、加
熱、紫外線、電子線などによって架橋されるが通常は加
熱による方法が一般的である。The crosslinking accelerator may be used alone, or in some cases, two or more types may be used in combination. The amount of crosslinking agent to be added is appropriately selected depending on the type of crosslinking agent, but usually poly(
It is preferably 0.01 to 50 parts by weight, and 0.1 to 50 parts by weight, based on 100 parts by weight of the solid content of the meth)acrylic acid ester copolymer.
-30 parts by weight is more preferred. If the amount added is less than 0.01 parts by weight, the crosslinking effect will be low, and if it exceeds 50 parts by weight, the adhesion of the heat-resistant coating layer will decrease, and furthermore, the coating properties will deteriorate, making it difficult to form a uniform layer. Further, as the crosslinking accelerator, known ones such as salts, inorganic substances, organic substances, acid substances, and alkaline substances can be used. The amount of the crosslinking promoter to be added is 0.00 parts by weight based on 100 parts by weight of the solid content of the poly(meth)acrylate copolymer containing the reactive monomer.
0.001 to 10 parts by weight, preferably 0.1 to 5 parts by weight. Poly(
After the meth)acrylic acid ester copolymer is applied to a substrate, it is crosslinked by heating, ultraviolet rays, electron beams, etc., but heating is usually the most common method.
本発明のバーコードラベルを構成する耐熱性プラスチッ
クフィルムの厚みは、特に限定されないか、1〜500
μmが好ましく、5〜300μmの範囲がより好ましく
基材ベースとしての実用面での取り扱い性に優れている
。The thickness of the heat-resistant plastic film constituting the barcode label of the present invention is not particularly limited, or is 1 to 500 mm thick.
It is preferably in the range of 5 to 300 μm, and more preferably in the range of 5 to 300 μm, as it is excellent in practical handling as a base material.
本発明のバーコードラベルを構成する耐熱性被覆層の積
層厚みは、特に限定されるものではないが、0.1〜5
0μmが好ましく、0.5〜20μmの範囲にあるもの
が耐熱性被覆層の均一形成性、密着性などの点で望まし
い。さらに耐熱性被覆層には必要に応じて、本発明の効
果を損わない範囲で公知の添加剤、例えば消泡剤、塗布
性改良剤、増粘剤、帯電防止剤、酸化防止剤、紫外線吸
収剤、染料、増白剤等を含有せしめてもよいし、滑剤と
して無機または有機化合物からなる微細粒子を含有せし
めてもよい。The laminated thickness of the heat-resistant coating layer constituting the barcode label of the present invention is not particularly limited, but is 0.1 to 5.
The thickness is preferably 0 μm, and preferably in the range of 0.5 to 20 μm from the viewpoint of uniform formation and adhesion of the heat-resistant coating layer. Furthermore, the heat-resistant coating layer may contain known additives, such as antifoaming agents, coating improvers, thickeners, antistatic agents, antioxidants, and ultraviolet rays, as long as they do not impair the effects of the present invention. It may contain an absorbent, a dye, a brightening agent, etc., or it may contain fine particles made of an inorganic or organic compound as a lubricant.
耐熱性被覆層の付加方式は通常知られた方法が有効に使
用される。例えば、グラビアコート法、リバースコート
法、キスコート法、ダイコート法、メタリングバーコー
ド法、ナイフコート法など公知の方法が適用できる。ま
た耐熱性被覆層を塗布する前に、必要に応じて空気中あ
るいはその他種々雰囲気中でのコロナ放電処理など公知
の表面処理を施すことによって、塗布性が良化するのみ
ならず、耐熱性被覆層をより強固に基材表面上に形成で
きる。尚、塗材濃度、塗膜乾燥条件は特にβ艮定されな
いか、塗膜乾燥条件は耐熱性被覆層や基体フィルt1の
緒特性に悪影響を及ぼさない範囲で行なうのか望ましい
。Generally known methods are effectively used to add the heat-resistant coating layer. For example, known methods such as a gravure coating method, a reverse coating method, a kiss coating method, a die coating method, a metal ring barcode method, and a knife coating method can be applied. Furthermore, before applying the heat-resistant coating layer, by performing a known surface treatment such as corona discharge treatment in air or other various atmospheres as necessary, not only the coating properties will be improved but also the heat-resistant coating will be A stronger layer can be formed on the surface of the base material. It is preferable that the coating material concentration and the coating film drying conditions are not particularly determined, or that the coating film drying conditions are carried out within a range that does not adversely affect the heat-resistant coating layer and the properties of the base film t1.
本発明における請求項2および4記載の耐熱・耐水・耐
洗剤性接着剤の耐熱性は150°C1好ましくは200
℃、より好ましくは240°Cである。また、粉石鹸、
合成洗剤、過酸化水素、次亜塩素酸などの洗剤や温水に
対して十分な耐久力を有することが望ましく、さらに綿
、テトロン、ナイロン等の布帛製品に張り付けた状態で
1kg7/25mm以上の剥離強度を有することが望ま
しい。The heat-resistant, water-resistant, and detergent-resistant adhesive according to claims 2 and 4 of the present invention has a heat resistance of 150°C, preferably 200°C.
℃, more preferably 240°C. Also, powdered soap,
It is desirable that it has sufficient durability against detergents such as synthetic detergents, hydrogen peroxide, and hypochlorous acid, as well as hot water, and it should also be able to withstand peeling of 1 kg 7/25 mm or more when attached to fabric products such as cotton, Tetoron, and nylon. It is desirable to have strength.
そのような接着剤としてはアクリル系(アクリル酸エス
テルアクリル共重合樹脂)、シリコーン系合成ゴム系(
スチレンブタジェンラバー(SBR))等があげられる
。Examples of such adhesives include acrylic (acrylic acid ester acrylic copolymer resin) and silicone synthetic rubber (
Examples include styrene butadiene rubber (SBR).
なお、耐熱性透明プラスチックフィルムおよび該耐熱性
透明プラスチックフィルムに塗設した接着剤は、バーコ
ードを読み取るために十分な透明性を有することが望ま
れる。Note that it is desirable that the heat-resistant transparent plastic film and the adhesive applied to the heat-resistant transparent plastic film have sufficient transparency to read the barcode.
バーコードインクは耐熱性か150°C1望ましくは2
00°C1より望ましくは240°C以上である。印字
方式としては、レーザー法、バブルジェット法、熱転写
法、インクジェット法、PPC法などがあげられる。こ
こで、バーコードの印字面積をフィルム全体の面積より
も小さく設定しておけば、ぬいしるの部分が確保され、
下記の縫い付けにおいて望ましい結果が得られる。Barcode ink is heat resistant or 150°C, preferably 2
The temperature is preferably 240°C or higher than 00°C1. Examples of printing methods include laser method, bubble jet method, thermal transfer method, inkjet method, and PPC method. If you set the printing area of the barcode to be smaller than the entire area of the film, the sewing area will be secured.
The desired result is obtained in the following stitches.
本発明のセパレータとは、本発明の耐熱・耐水・耐洗剤
性接着剤に異物の付着などによる接着作用の劣化を防ぐ
ために該耐熱・耐水・耐洗剤性接着剤層の表面を一時的
に保護する層であり、剥離しやすく、接着層のセパレー
タ側への転着がなく、寸法変化が少ないことが望ましい
。セパレータとして特に限定されるものではないが、シ
リコン系、フッ素樹脂系、またはワックス系の物質でコ
ーティングした紙フィルムやプラスチックフィルム等が
あげられる。The separator of the present invention is a separator that temporarily protects the surface of the heat-resistant, water-resistant, and detergent-resistant adhesive layer of the present invention in order to prevent deterioration of the adhesive action due to adhesion of foreign matter to the heat-resistant, water-resistant, and detergent-resistant adhesive layer. It is desirable that the adhesive layer be easily peeled off, that there will be no transfer of the adhesive layer to the separator side, and that there will be little dimensional change. Examples of the separator include, but are not particularly limited to, paper films and plastic films coated with silicone-based, fluororesin-based, or wax-based substances.
本発明における布帛としては特に限定されるものではな
いが、いわゆる衣服を始めとして、ホテル等で使用され
るリネン(シーツ、タオル1、テーブルクロス等)、病
院のリネン(シーツ、寝間着、白衣など)およびレスト
ランのお絞り、テーブルクロス等があげられる。The fabric in the present invention is not particularly limited, but includes so-called clothing, linen used in hotels (sheets, towels, tablecloths, etc.), hospital linen (sheets, nightwear, white coats, etc.) and restaurant towels, tablecloths, etc.
本発明における縫い付は糸および縫い付は法は特に限定
されるものではないが、綿、テトロン、ナイロンあるい
はそれらの混紡されたものなどを糸として用い、ミシン
などで縫い付ける方法があげられる。In the present invention, the sewing thread and sewing method are not particularly limited, but examples include a method of sewing with a sewing machine or the like using cotton, Tetoron, nylon, or a blend thereof as thread.
次に本発明の一態様を述べるが、特にこれに限定される
ものではない。Next, one embodiment of the present invention will be described, but the present invention is not particularly limited thereto.
まず、耐熱性プラスチックフィルムとして、フッ素樹脂
、ポリ−p−フェニレンスルフィドを主成分とする樹脂
組成物、分子中にイミド基を有する重合体、芳香族ポリ
アミド系重合体のいずれかからなるフィルムの少なくと
も一表面に対し、耐熱性被覆層としてポリ(メタ)アク
リル酸エステル共重合体を主成分とする組成物からなる
層、またはアルコキシシラン或いはグリシジル基を含有
する不飽和結合を有する化合物をグラフト化した非水系
ポリエステル共重合体を主成分とする組成物からなる層
を設ける。First, as a heat-resistant plastic film, at least one of a fluororesin, a resin composition containing poly-p-phenylene sulfide as a main component, a polymer having imide groups in the molecule, and an aromatic polyamide-based polymer is used. A layer consisting of a composition mainly composed of a poly(meth)acrylate copolymer, or a compound having an unsaturated bond containing an alkoxysilane or a glycidyl group is grafted onto one surface as a heat-resistant coating layer. A layer made of a composition containing a non-aqueous polyester copolymer as a main component is provided.
塗布方法は特に限定されず押出ラミネート法、メルトコ
ーティング法等を用いてもよいか、高速で薄膜コートす
ることか可能であるという理由からグラビヤコート法、
リバースコート法、キツスコート法、ダイコート法、メ
タリングバーコード法なと公知の方法を適用できる。ま
た、塗布する前に必要に応じて空気中或いはその他種々
雰囲気中でのコロナ放電処理など公知の表面処理を施す
ことによって、塗布性が良化するのみならず、耐熱性被
覆層をより強固に耐熱性プラスチックフィルム表面上に
形成できる。なお、塗材濃度、塗膜乾燥条件は特に限定
されるものではないが、塗膜乾燥条件は耐熱性被覆層や
基体フィルムの緒特性に悪影響を及ぼさない範囲で行な
うのが望ましいついで、耐熱性被覆層にバーコード印字
を行う。印字方法としてはオートニクス社BC−8Mk
■プリンターを用いる方法があげられる。The coating method is not particularly limited, and extrusion lamination, melt coating, etc. may be used, or high-speed thin film coating is possible.Gravure coating,
Known methods such as a reverse coating method, a kitsu coating method, a die coating method, and a metal ring bar code method can be applied. In addition, by performing known surface treatments such as corona discharge treatment in the air or in various other atmospheres as necessary before coating, not only will coating properties be improved, but the heat-resistant coating layer will also be made stronger. Can be formed on the surface of a heat-resistant plastic film. The coating material concentration and coating drying conditions are not particularly limited, but it is desirable to dry the coating within a range that does not adversely affect the heat-resistant coating layer or the properties of the base film. Print a barcode on the coating layer. The printing method is Autonics BC-8Mk.
■One method is to use a printer.
次に耐熱性プラスチックフィルムの印字面側に、接着層
を塗設して耐熱性透明プラスチックフィルム層を設け、
耐熱性プラスチックフィルムの反対側の面に接着層を介
してセパレート層を設ける。Next, an adhesive layer is applied to the printed side of the heat-resistant plastic film to form a heat-resistant transparent plastic film layer.
A separate layer is provided on the opposite side of the heat-resistant plastic film via an adhesive layer.
接着剤としてはアクリル系(アクリル酸エステルアクリ
ル共重合樹脂)、シリコーン系合成ゴム系(スチレンブ
タジェンラバー(SBR))等の接着剤があげられる。Examples of the adhesive include acrylic adhesives (acrylic ester acrylic copolymer resin), silicone synthetic rubber adhesives (styrene butadiene rubber (SBR)), and the like.
塗布方法は特に限定されず押出ラミネート法、メルトコ
ーティング法等を用いてもよいが、高速で薄膜コートす
ることか可能であるという理由からグラビヤコート法、
リバースコート法、キツスコート法、ダイコート法、メ
タリングバーコード法など公知の方法を適用できる。ま
た、塗布する前に必要に応じて空気中或いはその他種々
雰囲気中でのコロナ放電処理など公知の表面処理を施す
ことによって、塗布性が良化するのみならず、耐熱性被
覆層をより強固に耐熱性プラスチックフィルム表面上に
形成できる。尚、塗材濃度、塗膜乾燥条件は特に限定さ
れるものではないか、塗膜乾燥条件は耐熱性被覆層や基
体フィルムの諸特性に悪影響を及ぼさない範囲で行なう
のが望ましい。接着剤の塗布は、耐熱性プラスチックフ
ィルムと耐熱性透明プラスチックフィルムの互いに対向
する面の少なくとも一方の面、ならびに耐熱性プラスチ
ックフィルムとセパレート層の互いに対向する面の少な
くとも一方に行えば良い。The coating method is not particularly limited, and extrusion lamination method, melt coating method, etc. may be used, but gravure coating method, because it is possible to coat a thin film at high speed,
Known methods such as a reverse coat method, a kit coat method, a die coat method, and a metal ring bar code method can be applied. In addition, by performing known surface treatments such as corona discharge treatment in the air or in various other atmospheres as necessary before coating, not only will coating properties be improved, but the heat-resistant coating layer will also be made stronger. Can be formed on the surface of a heat-resistant plastic film. The coating material concentration and coating film drying conditions are not particularly limited, and it is desirable that the coating film drying conditions be within a range that does not adversely affect the properties of the heat-resistant coating layer and the base film. The adhesive may be applied to at least one of the opposing surfaces of the heat-resistant plastic film and the heat-resistant transparent plastic film, and to at least one of the opposing surfaces of the heat-resistant plastic film and the separate layer.
こうして製造されたバーコードラベルはセパレート層を
剥離して接着剤層を露出し、任意の布帛製品、例えば、
シーツ、タオル、テーブルクロス、寝間着、白衣、お絞
りなどに人力または機械により連続式により張り付ける
。もちろん、セパレート層を設けず、直接張り付けても
良い。あるいは前記積層工程は特に順序を限定されるも
のではないので、例えば、バーコードを布帛製品に張り
付けた後、接着剤を塗布し、耐熱性透明プラスチックフ
ィルムを張り付けても良く、また耐熱性透明プラスチッ
クフィルムか該耐熱性プラスチック、 フィルムより
も面積か大きくても良い。バーコードラベルを張り付け
た後、さらに綿、テトロン、ナイロン等の糸を用い、ミ
シンまたは人の手で縫い付けを行うと、耐久性か向上す
る。The thus produced barcode label can be used to peel off the separate layer to expose the adhesive layer, and can be applied to any fabric product, e.g.
It is applied continuously to sheets, towels, tablecloths, nightwear, white coats, diaphragms, etc. by hand or machine. Of course, it is also possible to paste directly without providing a separate layer. Alternatively, the order of the lamination process is not particularly limited, so for example, after pasting a barcode on a fabric product, an adhesive may be applied and a heat-resistant transparent plastic film is pasted, or a heat-resistant transparent plastic film may be pasted. The film or the heat-resistant plastic may have a larger area than the film. After pasting the barcode label, the durability can be improved by sewing it with a sewing machine or by hand using cotton, Tetron, nylon, etc. thread.
本発明の特性値は次の測定方法、評価基準による。The characteristic values of the present invention are based on the following measurement method and evaluation criteria.
(1)耐熱性
平織シーツに張り合わせた本発明のバーコードラベルを
シーツ面を下にして平面上に置き、20g / c m
2の圧力て200°C1分間加熱した。(1) Place the barcode label of the present invention pasted onto a heat-resistant plain weave sheet on a flat surface with the sheet side facing down, and weigh 20 g/cm
The mixture was heated at 200°C for 1 minute at a pressure of 2.
判定基準は、
フィルム ニ
良好(収縮率±5%以内) −−−−−−一〇劣る(収
縮率±5〜10%) −−−−−−△不良(収縮率±1
0%を越える、あるいは融解する) −−−−−−−−
−−−−−−−−−x接着剤 :
良好(180°剥離強度1kg7725mm以上) −
−−−−−−−−−−−−−−−−−−○劣る(180
°剥離強度500g、/25mm以上1kg/25mm
未満) −−−−−−−−△’不良(180°剥離強度
500g/25mm未満) −−−m−−−−−一−−
−−−−−−xインク 、バーコードを拡大鏡で肉視観
察して判定
印字性良好−一一一一一一〜−−−−−−−〇印字性劣
るーーーーーーーーーーーーーーー△印字性不良−−−
−−−−−−−−−−−−−−−x(2)耐水性
平織シーツに張り合わせたバーコードラベルを60℃の
水に30分間浸漬処理後、18o0剥離強度を測定した
。Judgment criteria are: Film 2 Good (shrinkage rate within ±5%) -------10 Poor (shrinkage rate ±5 to 10%) ----------△Poor (shrinkage rate ±1%)
(exceeds 0% or melts)
−−−−−−−−x Adhesive: Good (180° peel strength 1 kg 7725 mm or more) −
−−−−−−−−−−−−−−−−−○○ Inferior (180
°Peel strength 500g, /25mm or more 1kg/25mm
(less than 500g/25mm) ---m-----
−−−−−−x ink, visually inspect the barcode with a magnifying glass and judge that the printing quality is good. --- △ Poor printing quality ---
-------------x (2) A barcode label attached to a water-resistant plain weave sheet was immersed in water at 60°C for 30 minutes, and then the 18o0 peel strength was measured.
良好(1kg/25mm以上> −−−−−0劣る(5
00g/25mm以上1kg/25mm未満)−一−−
−−−−−−−−−−−△不良(500g/25mm未
iiSり −−−−X(3)耐洗剤性
手織シーツに張り合わせたバーコードラベルを水11に
対して1gの洗剤「アタック」 (花王株式会社製)を
溶した60℃の水に30分間浸漬処理し、1800剥離
強度を測定した。Good (1 kg/25 mm or more > ------0 Poor (5
00g/25mm or more and less than 1kg/25mm) -1--
−−−−−−−−−−−△Defective (500g/25mm less than iiS) --−−−X (manufactured by Kao Corporation) for 30 minutes in 60°C water, and the 1800 peel strength was measured.
良好(1kg/25mm以上)−−−−−−0劣る(5
00g、/25mm以上1kg、/25mm未満)−−
−−−−−−−−−−−一△不良(500g/25mm
未満)−一一一一×〔実施例〕
以下本発明を実施例に基いて説明する。Good (1kg/25mm or more) -------0 Poor (5
00g, /25mm or more 1kg, less than /25mm) --
−−−−−−−−−−−1△Defective (500g/25mm
(Less than)-1111× [Examples] The present invention will be described below based on Examples.
実施例1
厚さか75μmのフッ素フィルム(東し合成フィルム株
式会社製“トヨフロン”)をプラズマ処理した。Example 1 A fluorine film ("Toyoflon" manufactured by Toshi Gosei Film Co., Ltd.) having a thickness of about 75 μm was subjected to plasma treatment.
次に、トルエン/酢酸エチル=1/1の希釈溶媒中に、
熱架橋型アクリル樹脂(東し株式会社製“コータックス
”Tg=75℃)固形分60重量部に対して白色隠蔽顔
料の酸化チタン(平均粒径0、 3μm)か固形分当た
り40重量部となるように混練された組成で均一に分散
させ、濃度10重量%の塗剤を得た。この塗剤を前記フ
ィルムにグラビアコート方式で塗布し、塗布層を130
°Cで1分間乾燥させ、耐熱性被覆層か20μmのフィ
ルムを得た。Next, in a diluted solvent of toluene/ethyl acetate = 1/1,
Thermal crosslinking type acrylic resin (“Kotax” manufactured by Toshi Co., Ltd. Tg = 75°C) 60 parts by weight of solid content and 40 parts by weight of white hiding pigment titanium oxide (average particle size 0.3 μm) per solid content. The composition was kneaded so as to be uniformly dispersed, and a coating material having a concentration of 10% by weight was obtained. This coating agent was applied to the film using a gravure coating method to form a coating layer of 130%
It was dried for 1 minute at °C to obtain a film with a heat-resistant coating layer of 20 μm.
前記フィルムの耐熱性被覆層側にオートニクス社製BC
−8MkIIプリンター(リボンは凸版印刷株式会社製
HD、印字条件10.5V、4.25m5)を用いてバ
ーコードを印刷した。これをシートAとする。Autonics BC on the heat-resistant coating layer side of the film.
A barcode was printed using a -8MkII printer (ribbon was HD manufactured by Toppan Printing Co., Ltd., printing conditions were 10.5 V, 4.25 m5). This is called sheet A.
次に厚さ100μmのフッ素フィルム(東し合成フィル
ム株式会社製“トヨフロン”)をプラズマ処理し、アク
リル酸エステル接着剤(日本カーバイド工業株式会社製
)をコンマ方式で塗布し、塗布層を120℃で1分間乾
燥させ、耐熱性被覆層が40μmのシートを得た。これ
をシートBとする。Next, a 100 μm thick fluorine film (Toyoflon manufactured by Toshi Gosei Film Co., Ltd.) was plasma-treated, and an acrylic ester adhesive (manufactured by Nippon Carbide Industries Co., Ltd.) was applied using the comma method, and the coating layer was heated to 120°C. The sheet was dried for 1 minute to obtain a sheet having a heat-resistant coating layer of 40 μm. This is called sheet B.
シートAのバーコード印字面の反対面にシートBと同様
に接着剤を被覆させ、手織シーツに2kgのコムローラ
ー5往復で接着させた。その上にシートBを2kgのゴ
ムローラーで5往復で接着させた。The opposite side of the barcode printed side of Sheet A was coated with an adhesive in the same manner as Sheet B, and was adhered to a hand-woven sheet using a 2 kg comb roller 5 times. Sheet B was adhered thereon with a 2 kg rubber roller 5 times back and forth.
サラにバーコード印字部の周りをミシンで縫いつけをし
た。I used a sewing machine to sew around the barcode printing area on Sarah.
このバーコードラベルの耐熱性、耐水性、耐洗剤性を評
価した。結果は第1表に示す。The heat resistance, water resistance, and detergent resistance of this barcode label were evaluated. The results are shown in Table 1.
次にこのバーコードラベルを張り付けたシーツを洗濯機
MWX−450(東京洗染機械制作所製)で60℃、2
2分て選択、27分ですすぎ・脱水し、その後150℃
に加熱したローラープレス機で乾燥、プレスした。Next, the sheets with this barcode label pasted were placed in a washing machine MWX-450 (manufactured by Tokyo Sensen Kikai Seisakusho) at 60℃ for 2 hours.
Select for 2 minutes, rinse and dehydrate for 27 minutes, then heat at 150℃.
It was dried and pressed using a roller press machine heated to .
この洗濯工程を5回繰り返した後のバーコードラベルの
特性は第2表に示す。The characteristics of the barcode label after repeating this washing process five times are shown in Table 2.
本発明のバーコードラベルは耐熱性、耐水性、耐洗剤性
に優れているので、シーツ、タオル、テーブルクロス等
の布帛製品のクリーニングに対して十分な耐久性を有し
ている。Since the barcode label of the present invention has excellent heat resistance, water resistance, and detergent resistance, it has sufficient durability for cleaning fabric products such as sheets, towels, and tablecloths.
これらの特質より、本発明のバーコードラベルはホテル
、病院、レストラン等で使用されるシーツ、タオル、テ
ーブルクロス、寝間着、白衣等のクリーニングの管理に
好適である。Due to these characteristics, the barcode label of the present invention is suitable for managing the cleaning of sheets, towels, tablecloths, nightwear, white coats, etc. used in hotels, hospitals, restaurants, etc.
Claims (6)
層を塗設し、該耐熱性被覆層に耐熱性インクを用いてバ
ーコードを印字したことを特徴とするバーコードラベル
。(1) A barcode label characterized in that a heat-resistant coating layer is coated on one side of a heat-resistant plastic film, and a barcode is printed on the heat-resistant coating layer using heat-resistant ink.
層を塗設し、該被覆層に耐熱性インクを用いてバーコー
ドを印字し、さらにバーコード印字面に耐熱・耐水・耐
洗剤性接着剤を介して耐熱性透明プラスチックフィルム
を張り合わせたことを特徴とするバーコードラベル。(2) A heat-resistant coating layer is coated on one side of a heat-resistant plastic film, a barcode is printed on the coating layer using heat-resistant ink, and a heat-resistant, water-resistant, and detergent-resistant adhesive is applied to the barcode printing surface. A barcode label that is made of a heat-resistant transparent plastic film laminated with a .
層を塗設し、該耐熱性被覆層に耐熱性インクを用いてバ
ーコードを印字し、耐熱性プラスチックフィルム面に耐
熱・耐水・耐洗剤性の接着剤を塗設し、該接着剤の上に
セパレータを張り合わせたことを特徴とするバーコード
ラベル。(3) A heat-resistant coating layer is coated on one side of the heat-resistant plastic film, a barcode is printed on the heat-resistant coating layer using heat-resistant ink, and the heat-resistant plastic film surface is heat-resistant, water-resistant, and detergent-resistant. 1. A barcode label characterized in that an adhesive is applied and a separator is laminated on top of the adhesive.
層を塗設し、該耐熱性被覆層に耐熱性インクを用いてバ
ーコードを印字し、さらにバーコード印字面に耐熱・耐
水・耐洗剤性接着剤を介して耐熱性透明プラスチックフ
ィルムを張り合わせ、耐熱性プラスチックフィルム面に
耐熱・耐水・耐洗剤性の接着剤を塗設し、該接着剤の上
にセパレータを張り合わせたことを特徴とするバーコー
ドラベル。(4) A heat-resistant coating layer is coated on one side of a heat-resistant plastic film, a barcode is printed on the heat-resistant coating layer using heat-resistant ink, and the barcode-printed surface is heat-resistant, water-resistant, and detergent-resistant. A bar characterized in that heat-resistant transparent plastic films are pasted together via an adhesive, a heat-resistant, water-resistant, and detergent-resistant adhesive is applied to the surface of the heat-resistant plastic film, and a separator is pasted on top of the adhesive. code label.
性プラスチックフィルム面に耐熱・耐水・耐洗剤性の接
着剤を塗設し、該接着剤塗設面を布帛に張り付けたこと
を特徴とするバーコードラベル付き布帛。(5) A heat-resistant, water-resistant, and detergent-resistant adhesive is coated on the heat-resistant plastic film surface of the barcode label according to claim 1 or 2, and the adhesive-coated surface is attached to a fabric. Fabric with barcode label.
てバーコードラベルと布帛とを縫合わせることを特徴と
するバーコードラベル付き布帛。(6) A fabric with a barcode label according to claim 5, characterized in that the barcode label and the fabric are sewn together.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2326628A JPH04197300A (en) | 1990-11-28 | 1990-11-28 | Bar code label and cloth with bar code label |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2326628A JPH04197300A (en) | 1990-11-28 | 1990-11-28 | Bar code label and cloth with bar code label |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH04197300A true JPH04197300A (en) | 1992-07-16 |
Family
ID=18189920
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2326628A Pending JPH04197300A (en) | 1990-11-28 | 1990-11-28 | Bar code label and cloth with bar code label |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH04197300A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5813772A (en) * | 1995-06-07 | 1998-09-29 | Avery Dennison Corporation | Garment labeling system, equipment and method and elastomeric label for use therewith |
-
1990
- 1990-11-28 JP JP2326628A patent/JPH04197300A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5813772A (en) * | 1995-06-07 | 1998-09-29 | Avery Dennison Corporation | Garment labeling system, equipment and method and elastomeric label for use therewith |
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