NO832710L - Registreringsmateriale med termisk respons. - Google Patents
Registreringsmateriale med termisk respons.Info
- Publication number
- NO832710L NO832710L NO832710A NO832710A NO832710L NO 832710 L NO832710 L NO 832710L NO 832710 A NO832710 A NO 832710A NO 832710 A NO832710 A NO 832710A NO 832710 L NO832710 L NO 832710L
- Authority
- NO
- Norway
- Prior art keywords
- methyl
- bis
- hydroxyphenyl
- coating
- material according
- Prior art date
Links
- 239000000463 material Substances 0.000 title claims description 51
- 239000011248 coating agent Substances 0.000 claims description 27
- 238000000576 coating method Methods 0.000 claims description 27
- 239000000376 reactant Substances 0.000 claims description 25
- ABSADEGWUCXWPQ-UHFFFAOYSA-N 2-hydroxy-3-phenylnaphthalene-1-carboxylic acid Chemical compound C=1C2=CC=CC=C2C(C(=O)O)=C(O)C=1C1=CC=CC=C1 ABSADEGWUCXWPQ-UHFFFAOYSA-N 0.000 claims description 16
- 239000006185 dispersion Substances 0.000 claims description 16
- 239000000758 substrate Substances 0.000 claims description 16
- 239000011230 binding agent Substances 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 14
- 239000003593 chromogenic compound Substances 0.000 claims description 13
- 239000002245 particle Substances 0.000 claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 10
- -1 phenol compound Chemical class 0.000 claims description 10
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 7
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 7
- NPFYZDNDJHZQKY-UHFFFAOYSA-N 4-Hydroxybenzophenone Chemical compound C1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 NPFYZDNDJHZQKY-UHFFFAOYSA-N 0.000 claims description 4
- 150000002989 phenols Chemical group 0.000 claims description 4
- 239000000049 pigment Substances 0.000 claims description 4
- 239000001993 wax Substances 0.000 claims description 4
- 229920002472 Starch Polymers 0.000 claims description 3
- 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 claims description 3
- 238000003490 calendering Methods 0.000 claims description 3
- 239000008199 coating composition Substances 0.000 claims description 3
- 229920000609 methyl cellulose Polymers 0.000 claims description 3
- 239000001923 methylcellulose Substances 0.000 claims description 3
- 235000010981 methylcellulose Nutrition 0.000 claims description 3
- NCBWBDIAHIFFTE-UHFFFAOYSA-N propan-2-yl 4,4-bis(4-hydroxyphenyl)pentanoate Chemical compound C=1C=C(O)C=CC=1C(C)(CCC(=O)OC(C)C)C1=CC=C(O)C=C1 NCBWBDIAHIFFTE-UHFFFAOYSA-N 0.000 claims description 3
- 239000008107 starch Substances 0.000 claims description 3
- 235000019698 starch Nutrition 0.000 claims description 3
- ZXDDPOHVAMWLBH-UHFFFAOYSA-N 2,4-Dihydroxybenzophenone Chemical compound OC1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 ZXDDPOHVAMWLBH-UHFFFAOYSA-N 0.000 claims description 2
- VHLLJTHDWPAQEM-UHFFFAOYSA-N 4-[2-(4-hydroxyphenyl)-4-methylpentan-2-yl]phenol Chemical compound C=1C=C(O)C=CC=1C(C)(CC(C)C)C1=CC=C(O)C=C1 VHLLJTHDWPAQEM-UHFFFAOYSA-N 0.000 claims description 2
- QDBFRHGFMDYIIT-UHFFFAOYSA-N 5-chloro-3-methyl-1,2,4-oxadiazole Chemical compound CC1=NOC(Cl)=N1 QDBFRHGFMDYIIT-UHFFFAOYSA-N 0.000 claims description 2
- RCVMSMLWRJESQC-UHFFFAOYSA-N 7-[4-(diethylamino)-2-ethoxyphenyl]-7-(1-ethyl-2-methylindol-3-yl)furo[3,4-b]pyridin-5-one Chemical compound CCOC1=CC(N(CC)CC)=CC=C1C1(C=2C3=CC=CC=C3N(CC)C=2C)C2=NC=CC=C2C(=O)O1 RCVMSMLWRJESQC-UHFFFAOYSA-N 0.000 claims description 2
- KYNSBQPICQTCGU-UHFFFAOYSA-N Benzopyrane Chemical compound C1=CC=C2C=CCOC2=C1 KYNSBQPICQTCGU-UHFFFAOYSA-N 0.000 claims description 2
- SDDLEVPIDBLVHC-UHFFFAOYSA-N Bisphenol Z Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)CCCCC1 SDDLEVPIDBLVHC-UHFFFAOYSA-N 0.000 claims description 2
- 239000004354 Hydroxyethyl cellulose Substances 0.000 claims description 2
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 claims description 2
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 claims description 2
- 229920000881 Modified starch Polymers 0.000 claims description 2
- UPOSGCJFXWMIAZ-UHFFFAOYSA-N ethyl 4,4-bis(4-hydroxyphenyl)pentanoate Chemical compound C=1C=C(O)C=CC=1C(C)(CCC(=O)OCC)C1=CC=C(O)C=C1 UPOSGCJFXWMIAZ-UHFFFAOYSA-N 0.000 claims description 2
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 claims description 2
- 239000001863 hydroxypropyl cellulose Substances 0.000 claims description 2
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 claims description 2
- 239000000314 lubricant Substances 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 235000019426 modified starch Nutrition 0.000 claims description 2
- 235000019422 polyvinyl alcohol Nutrition 0.000 claims description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 claims 1
- 239000004368 Modified starch Substances 0.000 claims 1
- 229910000040 hydrogen fluoride Inorganic materials 0.000 claims 1
- 125000004464 hydroxyphenyl group Chemical group 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- QHDYIMWKSCJTIM-UHFFFAOYSA-N phenyl 1-hydroxynaphthalene-2-carboxylate Chemical group C1=CC2=CC=CC=C2C(O)=C1C(=O)OC1=CC=CC=C1 QHDYIMWKSCJTIM-UHFFFAOYSA-N 0.000 claims 1
- QZRKWJJMXHAQIY-UHFFFAOYSA-N propyl 4,4-bis(4-hydroxyphenyl)pentanoate Chemical compound C=1C=C(O)C=CC=1C(C)(CCC(=O)OCCC)C1=CC=C(O)C=C1 QZRKWJJMXHAQIY-UHFFFAOYSA-N 0.000 claims 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 claims 1
- 239000000123 paper Substances 0.000 description 8
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000007788 liquid Substances 0.000 description 5
- 238000003384 imaging method Methods 0.000 description 4
- 239000005995 Aluminium silicate Substances 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- 235000012211 aluminium silicate Nutrition 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000004927 clay Substances 0.000 description 3
- 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 3
- SULYEHHGGXARJS-UHFFFAOYSA-N 2',4'-dihydroxyacetophenone Chemical compound CC(=O)C1=CC=C(O)C=C1O SULYEHHGGXARJS-UHFFFAOYSA-N 0.000 description 2
- RGHHSNMVTDWUBI-UHFFFAOYSA-N 4-hydroxybenzaldehyde Chemical compound OC1=CC=C(C=O)C=C1 RGHHSNMVTDWUBI-UHFFFAOYSA-N 0.000 description 2
- VXIXUWQIVKSKSA-UHFFFAOYSA-N 4-hydroxycoumarin Chemical compound C1=CC=CC2=C1OC(=O)C=C2O VXIXUWQIVKSKSA-UHFFFAOYSA-N 0.000 description 2
- HSHNITRMYYLLCV-UHFFFAOYSA-N 4-methylumbelliferone Chemical compound C1=C(O)C=CC2=C1OC(=O)C=C2C HSHNITRMYYLLCV-UHFFFAOYSA-N 0.000 description 2
- NTDQQZYCCIDJRK-UHFFFAOYSA-N 4-octylphenol Chemical compound CCCCCCCCC1=CC=C(O)C=C1 NTDQQZYCCIDJRK-UHFFFAOYSA-N 0.000 description 2
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-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
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 239000002518 antifoaming agent Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000004816 latex Substances 0.000 description 2
- 229920000126 latex Polymers 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 229920003986 novolac Polymers 0.000 description 2
- RARSHUDCJQSEFJ-UHFFFAOYSA-N p-Hydroxypropiophenone Chemical compound CCC(=O)C1=CC=C(O)C=C1 RARSHUDCJQSEFJ-UHFFFAOYSA-N 0.000 description 2
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical class [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 2
- LIZLYZVAYZQVPG-UHFFFAOYSA-N (3-bromo-2-fluorophenyl)methanol Chemical compound OCC1=CC=CC(Br)=C1F LIZLYZVAYZQVPG-UHFFFAOYSA-N 0.000 description 1
- HPJMSFQWRMTUHT-UHFFFAOYSA-N (4-hydroxyphenyl)-(4-methylphenyl)methanone Chemical compound C1=CC(C)=CC=C1C(=O)C1=CC=C(O)C=C1 HPJMSFQWRMTUHT-UHFFFAOYSA-N 0.000 description 1
- JBQTZLNCDIFCCO-UHFFFAOYSA-N 1-(4-hydroxyphenyl)-2-phenylethan-1-one Chemical compound C1=CC(O)=CC=C1C(=O)CC1=CC=CC=C1 JBQTZLNCDIFCCO-UHFFFAOYSA-N 0.000 description 1
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 1
- QDAWXRKTSATEOP-UHFFFAOYSA-N 2-acetylbenzoic acid Chemical compound CC(=O)C1=CC=CC=C1C(O)=O QDAWXRKTSATEOP-UHFFFAOYSA-N 0.000 description 1
- ASLNDVUAZOHADR-UHFFFAOYSA-N 2-butyl-3-methylphenol Chemical compound CCCCC1=C(C)C=CC=C1O ASLNDVUAZOHADR-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- RKSBPFMNOJWYSB-UHFFFAOYSA-N 3,3-Bis(4-hydroxyphenyl)pentane Chemical compound C=1C=C(O)C=CC=1C(CC)(CC)C1=CC=C(O)C=C1 RKSBPFMNOJWYSB-UHFFFAOYSA-N 0.000 description 1
- CONFUNYOPVYVDC-UHFFFAOYSA-N 3,3-bis(1-ethyl-2-methylindol-3-yl)-2-benzofuran-1-one Chemical compound C1=CC=C2C(C3(C4=CC=CC=C4C(=O)O3)C3=C(C)N(C4=CC=CC=C43)CC)=C(C)N(CC)C2=C1 CONFUNYOPVYVDC-UHFFFAOYSA-N 0.000 description 1
- RXNYJUSEXLAVNQ-UHFFFAOYSA-N 4,4'-Dihydroxybenzophenone Chemical compound C1=CC(O)=CC=C1C(=O)C1=CC=C(O)C=C1 RXNYJUSEXLAVNQ-UHFFFAOYSA-N 0.000 description 1
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical compound C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 1
- MLDIQALUMKMHCC-UHFFFAOYSA-N 4,4-Bis(4-hydroxyphenyl)heptane Chemical compound C=1C=C(O)C=CC=1C(CCC)(CCC)C1=CC=C(O)C=C1 MLDIQALUMKMHCC-UHFFFAOYSA-N 0.000 description 1
- SVOBELCYOCEECO-UHFFFAOYSA-N 4-[1-(4-hydroxy-3-methylphenyl)cyclohexyl]-2-methylphenol Chemical compound C1=C(O)C(C)=CC(C2(CCCCC2)C=2C=C(C)C(O)=CC=2)=C1 SVOBELCYOCEECO-UHFFFAOYSA-N 0.000 description 1
- DUKMWXLEZOCRSO-UHFFFAOYSA-N 4-[2-(4-hydroxyphenyl)-1-phenylpropan-2-yl]phenol Chemical compound C=1C=C(O)C=CC=1C(C=1C=CC(O)=CC=1)(C)CC1=CC=CC=C1 DUKMWXLEZOCRSO-UHFFFAOYSA-N 0.000 description 1
- AILHFXWIRQYDCJ-UHFFFAOYSA-N 4-[2-(4-hydroxyphenyl)-5-methylhexan-2-yl]phenol Chemical compound C=1C=C(O)C=CC=1C(C)(CCC(C)C)C1=CC=C(O)C=C1 AILHFXWIRQYDCJ-UHFFFAOYSA-N 0.000 description 1
- IAMNVCJECQWBLZ-UHFFFAOYSA-N 4-hydroxy-2-methylacetophenone Chemical compound CC(=O)C1=CC=C(O)C=C1C IAMNVCJECQWBLZ-UHFFFAOYSA-N 0.000 description 1
- NLCOOYIZLNQIQU-UHFFFAOYSA-N 7-[4-(diethylamino)-2-ethoxyphenyl]-7-(2-methyl-1-octylindol-3-yl)furo[3,4-b]pyridin-5-one Chemical compound C12=CC=CC=C2N(CCCCCCCC)C(C)=C1C1(C2=NC=CC=C2C(=O)O1)C1=CC=C(N(CC)CC)C=C1OCC NLCOOYIZLNQIQU-UHFFFAOYSA-N 0.000 description 1
- HTVITOHKHWFJKO-UHFFFAOYSA-N Bisphenol B Chemical compound C=1C=C(O)C=CC=1C(C)(CC)C1=CC=C(O)C=C1 HTVITOHKHWFJKO-UHFFFAOYSA-N 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- IPAJDLMMTVZVPP-UHFFFAOYSA-N Crystal violet lactone Chemical compound C1=CC(N(C)C)=CC=C1C1(C=2C=CC(=CC=2)N(C)C)C2=CC=C(N(C)C)C=C2C(=O)O1 IPAJDLMMTVZVPP-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- MXRIRQGCELJRSN-UHFFFAOYSA-N O.O.O.[Al] Chemical compound O.O.O.[Al] MXRIRQGCELJRSN-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 150000001299 aldehydes Chemical class 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
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- HPTYUNKZVDYXLP-UHFFFAOYSA-N aluminum;trihydroxy(trihydroxysilyloxy)silane;hydrate Chemical compound O.[Al].[Al].O[Si](O)(O)O[Si](O)(O)O HPTYUNKZVDYXLP-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- YXVFYQXJAXKLAK-UHFFFAOYSA-N biphenyl-4-ol Chemical compound C1=CC(O)=CC=C1C1=CC=CC=C1 YXVFYQXJAXKLAK-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 229910052621 halloysite Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- QLNWXBAGRTUKKI-UHFFFAOYSA-N metacetamol Chemical compound CC(=O)NC1=CC=CC(O)=C1 QLNWXBAGRTUKKI-UHFFFAOYSA-N 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- JZCLWFULJLDXDT-UHFFFAOYSA-N methyl 4,4-bis(4-hydroxyphenyl)pentanoate Chemical compound C=1C=C(O)C=CC=1C(C)(CCC(=O)OC)C1=CC=C(O)C=C1 JZCLWFULJLDXDT-UHFFFAOYSA-N 0.000 description 1
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 1
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- KLAKIAVEMQMVBT-UHFFFAOYSA-N p-hydroxy-phenacyl alcohol Natural products OCC(=O)C1=CC=C(O)C=C1 KLAKIAVEMQMVBT-UHFFFAOYSA-N 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 125000005506 phthalide group Chemical group 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 150000003216 pyrazines Chemical class 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- WKEDVNSFRWHDNR-UHFFFAOYSA-N salicylanilide Chemical compound OC1=CC=CC=C1C(=O)NC1=CC=CC=C1 WKEDVNSFRWHDNR-UHFFFAOYSA-N 0.000 description 1
- 229950000975 salicylanilide Drugs 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000001040 synthetic pigment Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/30—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used using chemical colour formers
- B41M5/337—Additives; Binders
- B41M5/3375—Non-macromolecular compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
- Color Printing (AREA)
- Laminated Bodies (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US40167882A | 1982-07-26 | 1982-07-26 | |
| US06/478,199 US4470057A (en) | 1982-07-26 | 1983-03-24 | Thermally-responsive record material |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO832710L true NO832710L (no) | 1984-01-27 |
Family
ID=27017560
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO832710A NO832710L (no) | 1982-07-26 | 1983-07-25 | Registreringsmateriale med termisk respons. |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US4470057A (OSRAM) |
| EP (1) | EP0100196B1 (OSRAM) |
| AU (1) | AU560537B2 (OSRAM) |
| BR (1) | BR8303900A (OSRAM) |
| DE (1) | DE3364941D1 (OSRAM) |
| DK (1) | DK337683A (OSRAM) |
| ES (1) | ES524377A0 (OSRAM) |
| FI (1) | FI74242C (OSRAM) |
| GR (1) | GR79604B (OSRAM) |
| NO (1) | NO832710L (OSRAM) |
| PT (1) | PT77075B (OSRAM) |
Families Citing this family (34)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4586061A (en) * | 1984-11-09 | 1986-04-29 | Appleton Papers Inc. | Thermally-responsive record material |
| US4794102A (en) * | 1987-09-03 | 1988-12-27 | Appleton Papers Inc. | Thermally-responsive record material |
| GB8811965D0 (en) * | 1988-05-20 | 1988-06-22 | Wiggins Teape Group Ltd | Thermal record material |
| US4870047A (en) * | 1988-09-01 | 1989-09-26 | Appleton Papers Inc. | Thermally-responsive record material |
| US5164357A (en) * | 1991-06-05 | 1992-11-17 | Appleton Papers Inc. | Thermally-responsive record material |
| US5290704A (en) * | 1993-03-19 | 1994-03-01 | Valence Technology, Inc. | Method of detecting organic solvent vapors |
| US5601867A (en) * | 1995-06-22 | 1997-02-11 | The United States Of America As Represented By The Secretary Of The Navy | Method and apparatus for generating fingerprints and other skin prints |
| US6294502B1 (en) | 1998-05-22 | 2001-09-25 | Bayer Aktiengesellschaft | Thermally-responsive record material |
| US6407034B1 (en) | 1999-09-13 | 2002-06-18 | William D. Ewing | Thermal chromogenic plastic film and method of manufacture therefor |
| US6937153B2 (en) * | 2002-06-28 | 2005-08-30 | Appleton Papers Inc. | Thermal imaging paper laminate |
| MXPA05003557A (es) | 2002-10-02 | 2005-11-17 | Gen Data Co Inc | Formacion termica directa de imagen sobre pelicula plastica john finger. |
| US7108190B2 (en) * | 2003-02-28 | 2006-09-19 | Appleton Papers Inc. | Token array and method employing authentication tokens bearing scent formulation information |
| US7125824B2 (en) * | 2003-05-22 | 2006-10-24 | Appleton Papers Inc. | Linerless labels |
| US20040251309A1 (en) * | 2003-06-10 | 2004-12-16 | Appleton Papers Inc. | Token bearing magnetc image information in registration with visible image information |
| JP4851465B2 (ja) | 2004-11-08 | 2012-01-11 | フレッシュポイント・ホールディングス・ソシエテ・アノニム | 時間温度指示装置 |
| US8500895B2 (en) | 2006-05-22 | 2013-08-06 | Marken-Imaje Corporation | Methods of marking and related structures and compositions |
| US20080145940A1 (en) * | 2006-12-18 | 2008-06-19 | 3M Innovative Properties Company | Chemical indicator test strip |
| US20080145948A1 (en) * | 2006-12-18 | 2008-06-19 | 3M Innovative Properties Company | Chemical indicator test strip |
| US9418576B2 (en) * | 2008-05-14 | 2016-08-16 | Avery Dennison Corporation | Dissolvable thermal direct adhesive label and label assembly including the same |
| EP2288879B1 (en) | 2008-06-04 | 2018-01-24 | G Patel | A monitoring system based on etching of metals |
| EP3293493B1 (en) | 2008-06-04 | 2023-06-14 | Jp Laboratories, Inc. | Sterilization indicating device |
| US20100266322A1 (en) * | 2009-04-17 | 2010-10-21 | Timothy Croskey | Apparatus and method for destroying confidential medical information on labels for medicines |
| US9034790B2 (en) | 2013-03-14 | 2015-05-19 | Appvion, Inc. | Thermally-responsive record material |
| US9126451B2 (en) | 2013-12-18 | 2015-09-08 | Appvion, Inc. | Thermal recording materials |
| US9534156B2 (en) | 2014-09-17 | 2017-01-03 | Appvion, Inc. | Linerless record material |
| WO2019183471A1 (en) | 2018-03-23 | 2019-09-26 | Appvion Operations, Inc. | Direct thermal recording media based on selective change of state |
| US20200019077A1 (en) | 2018-07-11 | 2020-01-16 | Appvion Operations, Inc. | Media Adapted for Both Direct Thermal Recording and Memjet-Type Printing |
| EP4021734A1 (en) | 2019-09-25 | 2022-07-06 | Appvion, LLC | Direct thermal recording media with perforated particles |
| AU2020386970A1 (en) | 2019-11-22 | 2022-06-23 | Appvion, Llc | Water-dispersible direct thermal or inkjet printable media |
| US12115803B2 (en) | 2020-12-10 | 2024-10-15 | Appvion, Llc | Fade-resistant water-dispersible phenol-free direct thermal media |
| WO2022125104A1 (en) | 2020-12-10 | 2022-06-16 | Appvion, Llc | Multi-purpose phenol-free direct thermal recording media |
| DE202020006063U1 (de) | 2020-12-10 | 2024-08-27 | Appvion, Llc | Phenol-freie Mehrzweck-Thermodirekt-Aufzeichnungsmedien |
| US12151498B2 (en) | 2020-12-10 | 2024-11-26 | Appvion, Llc | Multi-purpose phenol-free direct thermal recording media |
| US20240059090A1 (en) | 2022-08-10 | 2024-02-22 | Appvion, Llc | Direct thermal recording media with diarylurea combinations for oil resistance |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5348751A (en) * | 1976-10-16 | 1978-05-02 | Kanzaki Paper Mfg Co Ltd | Heat sensitive recording member |
| JPS5764593A (en) * | 1980-10-09 | 1982-04-19 | Honshu Paper Co Ltd | Thermal recording pper |
| JPS57201693A (en) * | 1981-06-05 | 1982-12-10 | Ricoh Co Ltd | Heat-sensitive recording material |
| JPS5887094A (ja) * | 1981-11-18 | 1983-05-24 | Fuji Photo Film Co Ltd | 感熱記録材料 |
-
1983
- 1983-03-24 US US06/478,199 patent/US4470057A/en not_active Expired - Lifetime
- 1983-07-19 EP EP83304172A patent/EP0100196B1/en not_active Expired
- 1983-07-19 DE DE8383304172T patent/DE3364941D1/de not_active Expired
- 1983-07-19 GR GR71999A patent/GR79604B/el unknown
- 1983-07-20 BR BR8303900A patent/BR8303900A/pt unknown
- 1983-07-21 PT PT77075A patent/PT77075B/pt unknown
- 1983-07-22 DK DK337683A patent/DK337683A/da not_active Application Discontinuation
- 1983-07-22 FI FI832662A patent/FI74242C/fi not_active IP Right Cessation
- 1983-07-22 ES ES524377A patent/ES524377A0/es active Granted
- 1983-07-22 AU AU17214/83A patent/AU560537B2/en not_active Ceased
- 1983-07-25 NO NO832710A patent/NO832710L/no unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP0100196A3 (en) | 1984-04-04 |
| ES8502030A1 (es) | 1984-12-16 |
| FI832662A0 (fi) | 1983-07-22 |
| AU1721483A (en) | 1984-02-02 |
| GR79604B (OSRAM) | 1984-10-31 |
| DK337683A (da) | 1984-01-27 |
| EP0100196B1 (en) | 1986-07-30 |
| FI74242C (fi) | 1988-01-11 |
| DK337683D0 (da) | 1983-07-22 |
| FI832662L (fi) | 1984-01-27 |
| PT77075B (en) | 1986-02-26 |
| DE3364941D1 (en) | 1986-09-04 |
| EP0100196A2 (en) | 1984-02-08 |
| US4470057A (en) | 1984-09-04 |
| FI74242B (fi) | 1987-09-30 |
| PT77075A (en) | 1983-08-01 |
| BR8303900A (pt) | 1984-02-28 |
| AU560537B2 (en) | 1987-04-09 |
| ES524377A0 (es) | 1984-12-16 |
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