FI109191B - Tallennusmateriaali - Google Patents

Tallennusmateriaali Download PDF

Info

Publication number: FI109191B
Authority: FI; Finland
Prior art keywords: recording material; color; microcapsules; chromogen; melamine
Prior art date: 1992-09-10

Application number

FI933935A

Other languages

English (en)

Finnish (fi)

Swedish (sv)

Other versions

FI933935L (fi

FI933935A0 (fi

Inventor

Robert E Miller

Robert W Brown

Lowell Schleicher

Lucy Feldman

Original Assignee

Appleton Paper Inc

Priority date (The priority date 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 date listed.)

1992-09-10

Filing date

1993-09-08

Publication date

2002-06-14

1993-09-08 Application filed by Appleton Paper Inc filed Critical Appleton Paper Inc

1993-09-08 Publication of FI933935A0 publication Critical patent/FI933935A0/fi

1994-03-11 Publication of FI933935L publication Critical patent/FI933935L/fi

2002-06-14 Application granted granted Critical

2002-06-14 Publication of FI109191B publication Critical patent/FI109191B/fi

Links

239000000463 material Substances 0.000 title claims abstract description 55
239000003094 microcapsule Substances 0.000 claims abstract description 33
239000000758 substrate Substances 0.000 claims abstract description 18
239000000203 mixture Substances 0.000 claims abstract description 17
230000008859 change Effects 0.000 claims abstract description 9
-1 isopropyl xanthone Chemical compound 0.000 claims description 23
229920005989 resin Polymers 0.000 claims description 18
239000011347 resin Substances 0.000 claims description 18
238000000034 method Methods 0.000 claims description 14
229920000877 Melamine resin Polymers 0.000 claims description 13
JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims description 10
239000000178 monomer Substances 0.000 claims description 10
229920000642 polymer Polymers 0.000 claims description 9
DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical group C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 claims description 7
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 5
IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 claims description 5
238000006116 polymerization reaction Methods 0.000 claims description 5
230000008569 process Effects 0.000 claims description 5
MBHRHUJRKGNOKX-UHFFFAOYSA-N [(4,6-diamino-1,3,5-triazin-2-yl)amino]methanol Chemical compound NC1=NC(N)=NC(NCO)=N1 MBHRHUJRKGNOKX-UHFFFAOYSA-N 0.000 claims description 4
238000012546 transfer Methods 0.000 claims description 4
229920003180 amino resin Polymers 0.000 claims description 3
238000011161 development Methods 0.000 claims description 3
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 claims description 3
KWVGIHKZDCUPEU-UHFFFAOYSA-N 2,2-dimethoxy-2-phenylacetophenone Chemical compound C=1C=CC=CC=1C(OC)(OC)C(=O)C1=CC=CC=C1 KWVGIHKZDCUPEU-UHFFFAOYSA-N 0.000 claims description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
238000011065 in-situ storage Methods 0.000 claims description 2
JNELGWHKGNBSMD-UHFFFAOYSA-N xanthone powder Natural products C1=CC=C2C(=O)C3=CC=CC=C3OC2=C1 JNELGWHKGNBSMD-UHFFFAOYSA-N 0.000 claims description 2
238000005336 cracking Methods 0.000 claims 1
239000011888 foil Substances 0.000 claims 1
239000003999 initiator Substances 0.000 claims 1
238000004519 manufacturing process Methods 0.000 claims 1
229940096522 trimethylolpropane triacrylate Drugs 0.000 claims 1
230000005855 radiation Effects 0.000 abstract description 6
238000003384 imaging method Methods 0.000 abstract description 2
239000002775 capsule Substances 0.000 description 31
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 18
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 14
239000008384 inner phase Substances 0.000 description 13
238000000576 coating method Methods 0.000 description 12
150000001875 compounds Chemical class 0.000 description 10
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
230000002378 acidificating effect Effects 0.000 description 9
229920002451 polyvinyl alcohol Polymers 0.000 description 8
239000011248 coating agent Substances 0.000 description 7
239000006185 dispersion Substances 0.000 description 7
229910000040 hydrogen fluoride Inorganic materials 0.000 description 7
239000000839 emulsion Substances 0.000 description 6
238000005538 encapsulation Methods 0.000 description 6
239000010410 layer Substances 0.000 description 6
239000002245 particle Substances 0.000 description 6
GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 6
239000007787 solid Substances 0.000 description 6
238000003756 stirring Methods 0.000 description 6
238000006243 chemical reaction Methods 0.000 description 5
239000003795 chemical substances by application Substances 0.000 description 5
239000000084 colloidal system Substances 0.000 description 5
229920001568 phenolic resin Polymers 0.000 description 5
238000002360 preparation method Methods 0.000 description 5
239000002904 solvent Substances 0.000 description 5
230000008646 thermal stress Effects 0.000 description 5
229920003270 Cymel® Polymers 0.000 description 4
229920003261 Durez Polymers 0.000 description 4
239000002609 medium Substances 0.000 description 4
238000002844 melting Methods 0.000 description 4
230000008018 melting Effects 0.000 description 4
KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical class F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 3
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 3
239000002253 acid Substances 0.000 description 3
239000004202 carbamide Substances 0.000 description 3
125000004432 carbon atom Chemical group C* 0.000 description 3
SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 3
239000002184 metal Substances 0.000 description 3
229910052751 metal Inorganic materials 0.000 description 3
239000008385 outer phase Substances 0.000 description 3
239000012071 phase Substances 0.000 description 3
239000005011 phenolic resin Substances 0.000 description 3
230000035945 sensitivity Effects 0.000 description 3
239000000243 solution Substances 0.000 description 3
230000035882 stress Effects 0.000 description 3
239000000126 substance Substances 0.000 description 3
229920001187 thermosetting polymer Polymers 0.000 description 3
LIZLYZVAYZQVPG-UHFFFAOYSA-N (3-bromo-2-fluorophenyl)methanol Chemical compound OCC1=CC=CC(Br)=C1F LIZLYZVAYZQVPG-UHFFFAOYSA-N 0.000 description 2
WNZQDUSMALZDQF-UHFFFAOYSA-N 2-benzofuran-1(3H)-one Chemical compound C1=CC=C2C(=O)OCC2=C1 WNZQDUSMALZDQF-UHFFFAOYSA-N 0.000 description 2
MEQQLDKBWPZDGF-UHFFFAOYSA-N 3,3-bis(1h-indol-3-yl)-2-benzofuran-1-one Chemical compound C12=CC=CC=C2C(=O)OC1(C=1C2=CC=CC=C2NC=1)C1=CNC2=CC=CC=C12 MEQQLDKBWPZDGF-UHFFFAOYSA-N 0.000 description 2
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
239000005977 Ethylene Substances 0.000 description 2
SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
229920001807 Urea-formaldehyde Polymers 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
125000003368 amide group Chemical group 0.000 description 2
239000008346 aqueous phase Substances 0.000 description 2
239000007864 aqueous solution Substances 0.000 description 2
239000012965 benzophenone Substances 0.000 description 2
150000008366 benzophenones Chemical class 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
230000015556 catabolic process Effects 0.000 description 2
239000003593 chromogenic compound Substances 0.000 description 2
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
238000004945 emulsification Methods 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
239000008098 formaldehyde solution Substances 0.000 description 2
UMGLBLXWFVODRF-UHFFFAOYSA-N formaldehyde;4-phenylphenol Chemical compound O=C.C1=CC(O)=CC=C1C1=CC=CC=C1 UMGLBLXWFVODRF-UHFFFAOYSA-N 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
239000007788 liquid Substances 0.000 description 2
230000007246 mechanism Effects 0.000 description 2
229920000728 polyester Polymers 0.000 description 2
ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 2
239000002243 precursor Substances 0.000 description 2
150000003254 radicals Chemical class 0.000 description 2
230000002829 reductive effect Effects 0.000 description 2
230000004044 response Effects 0.000 description 2
230000002441 reversible effect Effects 0.000 description 2
YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
238000012360 testing method Methods 0.000 description 2
238000001931 thermography Methods 0.000 description 2
QTKIQLNGOKOPOE-UHFFFAOYSA-N 1,1'-biphenyl;propane Chemical group CCC.C1=CC=CC=C1C1=CC=CC=C1 QTKIQLNGOKOPOE-UHFFFAOYSA-N 0.000 description 1
WFOQXUOOXMEVQB-UHFFFAOYSA-N 1-butan-2-yl-2-phenylbenzene Chemical group CCC(C)C1=CC=CC=C1C1=CC=CC=C1 WFOQXUOOXMEVQB-UHFFFAOYSA-N 0.000 description 1
BUZMJVBOGDBMGI-UHFFFAOYSA-N 1-phenylpropylbenzene Chemical compound C=1C=CC=CC=1C(CC)C1=CC=CC=C1 BUZMJVBOGDBMGI-UHFFFAOYSA-N 0.000 description 1
JCTXKRPTIMZBJT-UHFFFAOYSA-N 2,2,4-trimethylpentane-1,3-diol Chemical compound CC(C)C(O)C(C)(C)CO JCTXKRPTIMZBJT-UHFFFAOYSA-N 0.000 description 1
OYKPJMYWPYIXGG-UHFFFAOYSA-N 2,2-dimethylbutane;prop-2-enoic acid Chemical compound OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.CCC(C)(C)C OYKPJMYWPYIXGG-UHFFFAOYSA-N 0.000 description 1
HWSSEYVMGDIFMH-UHFFFAOYSA-N 2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOC(=O)C(C)=C HWSSEYVMGDIFMH-UHFFFAOYSA-N 0.000 description 1
XCIYATDPBXBBEW-UHFFFAOYSA-N 2-[4-(diethylamino)-2-ethoxyphenyl]-7h-furo[3,4-b]pyridin-5-one Chemical compound CCOC1=CC(N(CC)CC)=CC=C1C1=CC=C(C(=O)OC2)C2=N1 XCIYATDPBXBBEW-UHFFFAOYSA-N 0.000 description 1
ZCDADJXRUCOCJE-UHFFFAOYSA-N 2-chlorothioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(Cl)=CC=C3SC2=C1 ZCDADJXRUCOCJE-UHFFFAOYSA-N 0.000 description 1
QKTWWGYCVXCKOJ-UHFFFAOYSA-N 2-methoxy-1-(2-methoxyphenyl)-2-phenylethanone Chemical compound C=1C=CC=CC=1C(OC)C(=O)C1=CC=CC=C1OC QKTWWGYCVXCKOJ-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
KTALPKYXQZGAEG-UHFFFAOYSA-N 2-propan-2-ylthioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(C(C)C)=CC=C3SC2=C1 KTALPKYXQZGAEG-UHFFFAOYSA-N 0.000 description 1
RMZZBGUNXMGXCD-UHFFFAOYSA-N 3',6,6'-tris(dimethylamino)spiro[2-benzofuran-3,9'-fluorene]-1-one Chemical compound C12=CC=C(N(C)C)C=C2C2=CC(N(C)C)=CC=C2C21OC(=O)C1=CC(N(C)C)=CC=C21 RMZZBGUNXMGXCD-UHFFFAOYSA-N 0.000 description 1
SJEDSCUEKNQKRX-UHFFFAOYSA-N 3,3-bis[4-(diethylamino)phenyl]-6-(dimethylamino)-2-benzofuran-1-one Chemical compound C1=CC(N(CC)CC)=CC=C1C1(C=2C=CC(=CC=2)N(CC)CC)C2=CC=C(N(C)C)C=C2C(=O)O1 SJEDSCUEKNQKRX-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
ADEKJVNFIQUGRR-UHFFFAOYSA-N 4h-pyridin-3-one Chemical compound O=C1CC=CN=C1 ADEKJVNFIQUGRR-UHFFFAOYSA-N 0.000 description 1
KYNSBQPICQTCGU-UHFFFAOYSA-N Benzopyrane Chemical compound C1=CC=C2C=CCOC2=C1 KYNSBQPICQTCGU-UHFFFAOYSA-N 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
229920000298 Cellophane Polymers 0.000 description 1
241000767925 Collodes Species 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
XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 description 1
MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
239000004593 Epoxy Substances 0.000 description 1
JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 1
239000004640 Melamine resin Substances 0.000 description 1
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
239000004677 Nylon Substances 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
239000004743 Polypropylene Substances 0.000 description 1
239000004793 Polystyrene Substances 0.000 description 1
239000004372 Polyvinyl alcohol Substances 0.000 description 1
229920003265 Resimene® Polymers 0.000 description 1
206010070834 Sensitisation Diseases 0.000 description 1
239000007983 Tris buffer Substances 0.000 description 1
ZSOXNXDUYPYGJO-UHFFFAOYSA-N [2-(chloromethyl)phenyl]-phenylmethanone Chemical class ClCC1=CC=CC=C1C(=O)C1=CC=CC=C1 ZSOXNXDUYPYGJO-UHFFFAOYSA-N 0.000 description 1
238000005299 abrasion Methods 0.000 description 1
DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
150000001241 acetals Chemical class 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
229920000180 alkyd Polymers 0.000 description 1
150000004996 alkyl benzenes Chemical class 0.000 description 1
150000001350 alkyl halides Chemical class 0.000 description 1
150000001450 anions Chemical class 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
239000012736 aqueous medium Substances 0.000 description 1
150000001491 aromatic compounds Chemical class 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
230000004888 barrier function Effects 0.000 description 1
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical class OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
SESFRYSPDFLNCH-UHFFFAOYSA-N benzyl benzoate Chemical class C=1C=CC=CC=1C(=O)OCC1=CC=CC=C1 SESFRYSPDFLNCH-UHFFFAOYSA-N 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
239000013590 bulk material Substances 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
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230000009849 deactivation Effects 0.000 description 1
150000001983 dialkylethers Chemical class 0.000 description 1
125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 1
DROMNWUQASBTFM-UHFFFAOYSA-N dinonyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCC DROMNWUQASBTFM-UHFFFAOYSA-N 0.000 description 1
238000002845 discoloration Methods 0.000 description 1
YCZJVRCZIPDYHH-UHFFFAOYSA-N ditridecyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCCCCCC YCZJVRCZIPDYHH-UHFFFAOYSA-N 0.000 description 1
KWKXNDCHNDYVRT-UHFFFAOYSA-N dodecylbenzene Chemical compound CCCCCCCCCCCCC1=CC=CC=C1 KWKXNDCHNDYVRT-UHFFFAOYSA-N 0.000 description 1
239000000428 dust Substances 0.000 description 1
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150000002170 ethers Chemical class 0.000 description 1
MFGZXPGKKJMZIY-UHFFFAOYSA-N ethyl 5-amino-1-(4-sulfamoylphenyl)pyrazole-4-carboxylate Chemical compound NC1=C(C(=O)OCC)C=NN1C1=CC=C(S(N)(=O)=O)C=C1 MFGZXPGKKJMZIY-UHFFFAOYSA-N 0.000 description 1
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150000008376 fluorenones Chemical class 0.000 description 1
NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 1
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238000009472 formulation Methods 0.000 description 1
ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
238000000227 grinding Methods 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
238000010505 homolytic fission reaction Methods 0.000 description 1
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239000000852 hydrogen donor Substances 0.000 description 1
239000012216 imaging agent Substances 0.000 description 1
PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 1
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239000011810 insulating material Substances 0.000 description 1
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150000003951 lactams Chemical group 0.000 description 1
150000002596 lactones Chemical group 0.000 description 1
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238000005259 measurement Methods 0.000 description 1
150000007974 melamines Chemical class 0.000 description 1
239000000155 melt Substances 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
238000002156 mixing Methods 0.000 description 1
150000002790 naphthalenes Chemical class 0.000 description 1
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
229920001778 nylon Polymers 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
FZUGPQWGEGAKET-UHFFFAOYSA-N parbenate Chemical compound CCOC(=O)C1=CC=C(N(C)C)C=C1 FZUGPQWGEGAKET-UHFFFAOYSA-N 0.000 description 1
238000000059 patterning Methods 0.000 description 1
230000035515 penetration Effects 0.000 description 1
230000035699 permeability Effects 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
208000017983 photosensitivity disease Diseases 0.000 description 1
231100000434 photosensitization Toxicity 0.000 description 1
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239000004417 polycarbonate Substances 0.000 description 1
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229920001296 polysiloxane Polymers 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
108090000623 proteins and genes Proteins 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
229960004889 salicylic acid Drugs 0.000 description 1
239000004576 sand Substances 0.000 description 1
230000008313 sensitization Effects 0.000 description 1
125000003003 spiro group Chemical group 0.000 description 1
239000011232 storage material Substances 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
125000005420 sulfonamido group Chemical group S(=O)(=O)(N*)* 0.000 description 1
150000003457 sulfones Chemical group 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
150000001911 terphenyls Chemical class 0.000 description 1
238000010998 test method Methods 0.000 description 1
229920001169 thermoplastic Polymers 0.000 description 1
239000004416 thermosoftening plastic Substances 0.000 description 1
150000004897 thiazines Chemical class 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
239000001993 wax Substances 0.000 description 1
125000001834 xanthenyl group Chemical class C1=CC=CC=2OC3=CC=CC=C3C(C12)* 0.000 description 1
150000007964 xanthones Chemical class 0.000 description 1

Classifications

- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/002—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor using materials containing microcapsules; Preparing or processing such materials, e.g. by pressure; Devices or apparatus specially designed therefor
- 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
- B41M5/28—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used using thermochromic compounds or layers containing liquid crystals, microcapsules, bleachable dyes or heat- decomposable compounds, e.g. gas- liberating
- B41M5/287—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used using thermochromic compounds or layers containing liquid crystals, microcapsules, bleachable dyes or heat- decomposable compounds, e.g. gas- liberating using microcapsules or microspheres only
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
- Y10S430/165—Thermal imaging composition

Landscapes

Physics & Mathematics (AREA)
General Physics & Mathematics (AREA)
Optics & Photonics (AREA)
Heat Sensitive Colour Forming Recording (AREA)
Thermal Transfer Or Thermal Recording In General (AREA)
Color Printing (AREA)
Photoreceptors In Electrophotography (AREA)
Materials For Medical Uses (AREA)
Developing Agents For Electrophotography (AREA)
Materials For Photolithography (AREA)
Photosensitive Polymer And Photoresist Processing (AREA)
Medicines Containing Plant Substances (AREA)

FI933935A 1992-09-10 1993-09-08 Tallennusmateriaali FI109191B (fi)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US07/943,090 US5340680A (en)	1992-09-10	1992-09-10	Desensitizable record material
US94309092		1992-09-10

Publications (3)

Publication Number	Publication Date
FI933935A0 FI933935A0 (fi)	1993-09-08
FI933935L FI933935L (fi)	1994-03-11
FI109191B true FI109191B (fi)	2002-06-14

Family

ID=25479088

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
FI933935A FI109191B (fi)	1992-09-10	1993-09-08	Tallennusmateriaali

Country Status (8)

Country	Link
US (2)	US5340680A (de)
EP (1)	EP0587410B1 (de)
JP (1)	JP3441493B2 (de)
AT (1)	ATE162139T1 (de)
CA (1)	CA2092233C (de)
DE (1)	DE69316294T2 (de)
ES (1)	ES2111135T3 (de)
FI (1)	FI109191B (de)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5985526A (en) *	1998-06-19	1999-11-16	Eastman Kodak Company	Imaging process based on change of optical covering power
US6103378A (en) *	1998-11-23	2000-08-15	The Mead Company	Capsules having discrete solvent/color former and diluent capsule encapsulated phases
TW574112B (en) *	2000-06-01	2004-02-01	Sipix Imaging Inc	Imaging media containing heat developable photosensitive microcapsules and an imaging process of the imaging media
GB2396355A (en) *	2002-12-20	2004-06-23	Arjo Wiggins Fine Papers Ltd	Digital press printing composition and system
US7815723B2 (en) *	2006-04-19	2010-10-19	Crayola Llc	Water-based ink system
US7727319B2 (en) *	2006-04-19	2010-06-01	Crayola Llc	Water-based ink system
ES2641464T3 (es)	2011-12-15	2017-11-10	Fujifilm Hunt Chemicals U.S.A., Inc.	Sistema disolvente de baja toxicidad para resinas de poliamidaimida y fabricación de sistemas disolventes
WO2013109268A1 (en) *	2012-01-18	2013-07-25	Fujifilm Hunt Chemicals U.S.A., Inc.	Chemical coating composition for forming a laser-markable material and a laser-markable material
US9815941B2 (en)	2014-04-17	2017-11-14	Cymer-Dayton, Llc	Low toxicity solvent system for polyamdieimide and polyamide amic acid resin manufacture
US9725617B2 (en)	2014-04-17	2017-08-08	Fujifilm Hunt Chemicals U.S.A., Inc.	Low toxicity solvent system for polyamideimide and polyamide amic acid resin coating

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* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CH395152A (fr) *	1959-07-16	1965-07-15	Ncr Co	Procédé d'impression
US4343885A (en) *	1978-05-09	1982-08-10	Dynachem Corporation	Phototropic photosensitive compositions containing fluoran colorformer
US4454083A (en) *	1981-12-21	1984-06-12	Appleton Papers Inc.	Continuous microencapsulation
JPS5991438A (ja) *	1982-11-17	1984-05-26	Fuji Photo Film Co Ltd	感光感熱記録材料
US4552811A (en) *	1983-07-26	1985-11-12	Appleton Papers Inc.	Capsule manufacture
JPS60242094A (ja) *	1984-05-17	1985-12-02	Fuji Photo Film Co Ltd	感熱記録材料
EP0203613B1 (de) *	1985-05-30	1989-10-25	Fuji Photo Film Co., Ltd.	Mikrokapseln enthaltendes lichtempfindliches Material und dieses benutzendes Bildaufzeichnungsverfahren
JPS6297638A (ja) *	1985-10-25	1987-05-07	Kanzaki Paper Mfg Co Ltd	マイクロカプセルの製造方法
JPS63268777A (ja) *	1987-04-25	1988-11-07	Kanzaki Paper Mfg Co Ltd	マイクロカプセルインキ組成物
JPH07101314B2 (ja) *	1987-09-03	1995-11-01	富士写真フイルム株式会社	画像記録方法
GB2210702B (en) *	1987-10-02	1991-11-06	Fuji Photo Film Co Ltd	Heat sensitive recording material
US4873168A (en) *	1988-03-07	1989-10-10	The Mead Corporation	Imaging system utilizing heat treatment
US5134052A (en) *	1988-10-25	1992-07-28	The Mead Corporation	Process for forming images using a low temperature exposure step
US4937119A (en) *	1988-12-15	1990-06-26	Hoechst Celanese Corp.	Textured organic optical data storage media and methods of preparation
US5283015A (en) *	1989-03-15	1994-02-01	The Mead Corporation	Method for producing amine-formaldehyde microcapsules and photosensitive microcapsules produced thereby
JPH03261588A (ja) *	1990-03-12	1991-11-21	Kanzaki Paper Mfg Co Ltd	感圧複写紙の製造方法

1992
- 1992-09-10 US US07/943,090 patent/US5340680A/en not_active Expired - Lifetime
1993
- 1993-03-23 CA CA002092233A patent/CA2092233C/en not_active Expired - Lifetime
- 1993-09-06 JP JP24591793A patent/JP3441493B2/ja not_active Expired - Fee Related
- 1993-09-07 DE DE69316294T patent/DE69316294T2/de not_active Expired - Fee Related
- 1993-09-07 ES ES93307059T patent/ES2111135T3/es not_active Expired - Lifetime
- 1993-09-07 AT AT93307059T patent/ATE162139T1/de not_active IP Right Cessation
- 1993-09-07 EP EP93307059A patent/EP0587410B1/de not_active Expired - Lifetime
- 1993-09-08 FI FI933935A patent/FI109191B/fi active
1994
- 1994-03-09 US US08/208,395 patent/US5427886A/en not_active Expired - Lifetime

Also Published As

Publication number	Publication date
JP3441493B2 (ja)	2003-09-02
EP0587410A3 (en)	1996-03-27
DE69316294D1 (de)	1998-02-19
DE69316294T2 (de)	1998-04-30
US5340680A (en)	1994-08-23
CA2092233C (en)	2003-12-09
FI933935L (fi)	1994-03-11
EP0587410A2 (de)	1994-03-16
ATE162139T1 (de)	1998-01-15
US5427886A (en)	1995-06-27
JPH06206379A (ja)	1994-07-26
ES2111135T3 (es)	1998-03-01
CA2092233A1 (en)	1994-03-11
EP0587410B1 (de)	1998-01-14
FI933935A0 (fi)	1993-09-08

Publication	Publication Date	Title
US4742043A (en)	1988-05-03	Heat-sensitive recording material
KR20030053472A (ko)	2003-06-28	감열 현상용 감광성 마이크로캡슐을 함유하는 영상화 매체
FI109191B (fi)	2002-06-14	Tallennusmateriaali
US4585483A (en)	1986-04-29	Recording materials
EP0461651B1 (de)	1994-02-16	Aufzeichnungsmaterial
JP3614931B2 (ja)	2005-01-26	記録シートおよび偽造検知方法
US4920091A (en)	1990-04-24	Recording material
FI109190B (fi)	2002-06-14	Latentin kuvan vastaanottava arkki
JPH0151820B2 (de)	1989-11-06
JPS645688B2 (de)	1989-01-31
US4800193A (en)	1989-01-24	Recording material
JP3414940B2 (ja)	2003-06-09	感熱感圧記録材料及び画像記録方法
JP3373669B2 (ja)	2003-02-04	感熱記録材料及びその製造方法
JPH0939385A (ja)	1997-02-10	感熱感圧記録材料及び画像記録方法
JP3235690B2 (ja)	2001-12-04	感熱記録体
JPH02227284A (ja)	1990-09-10	感熱記録体
JPH05278342A (ja)	1993-10-26	感熱記録体
JP2005330291A (ja)	2005-12-02	新規ウレアウレタン化合物
JPS62113588A (ja)	1987-05-25	感熱記録材料
JPH0872397A (ja)	1996-03-19	感熱記録体及びその製造方法並びにその感熱記録体の記録方法
JPH08183248A (ja)	1996-07-16	自己発色性感圧記録シート及びその製造方法並びにその自己発色性感圧記録シートの記録方法
JPH04195047A (ja)	1992-07-15	記録材料
JP2003211853A (ja)	2003-07-30	透明感熱記録体
JPS63193882A (ja)	1988-08-11	記録材料
JPH04195048A (ja)	1992-07-15	記録材料