CN1158660A - 可采用激光的热敏元件 - Google Patents

可采用激光的热敏元件 Download PDF

Info

Publication number: CN1158660A
Authority: CN; China
Prior art keywords: silver; dyestuff; alkyl; image density; radiation
Prior art date: 1994-09-27
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

Application number

CN95195324A

Other languages

English (en)

Chinese (zh)

Inventor

R·E·比利斯

D·C·威格尔

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

EMISON CORP

Original Assignee

EMISON CORP

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.)

1994-09-27

Filing date

1995-08-01

Publication date

1997-09-03

1995-08-01 Application filed by EMISON CORP filed Critical EMISON CORP

1997-09-03 Publication of CN1158660A publication Critical patent/CN1158660A/zh

Status Pending legal-status Critical Current

Links

238000003384 imaging method Methods 0.000 claims abstract description 82
230000005855 radiation Effects 0.000 claims abstract description 31
GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 claims abstract description 31
FOIXSVOLVBLSDH-UHFFFAOYSA-N Silver ion Chemical compound [Ag+] FOIXSVOLVBLSDH-UHFFFAOYSA-N 0.000 claims abstract description 17
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 111
239000000975 dye Substances 0.000 claims description 105
238000000034 method Methods 0.000 claims description 51
239000000463 material Substances 0.000 claims description 41
-1 carbamide compound Chemical class 0.000 claims description 35
206010034972 Photosensitivity reaction Diseases 0.000 claims description 34
230000036211 photosensitivity Effects 0.000 claims description 33
KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 claims description 28
150000003378 silver Chemical class 0.000 claims description 27
229910052799 carbon Inorganic materials 0.000 claims description 22
238000010521 absorption reaction Methods 0.000 claims description 21
239000007767 bonding agent Substances 0.000 claims description 21
229910052739 hydrogen Inorganic materials 0.000 claims description 18
KAMAPADCIHYSMA-UHFFFAOYSA-N docosanoic acid;silver Chemical compound [Ag].CCCCCCCCCCCCCCCCCCCCCC(O)=O KAMAPADCIHYSMA-UHFFFAOYSA-N 0.000 claims description 17
239000001257 hydrogen Substances 0.000 claims description 17
230000002829 reductive effect Effects 0.000 claims description 17
239000003795 chemical substances by application Substances 0.000 claims description 16
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 16
125000004432 carbon atom Chemical group C* 0.000 claims description 15
HNYOPLTXPVRDBG-UHFFFAOYSA-N barbituric acid Chemical compound O=C1CC(=O)NC(=O)N1 HNYOPLTXPVRDBG-UHFFFAOYSA-N 0.000 claims description 14
238000011161 development Methods 0.000 claims description 14
229960002317 succinimide Drugs 0.000 claims description 14
SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims description 13
125000000217 alkyl group Chemical group 0.000 claims description 13
150000001875 compounds Chemical class 0.000 claims description 13
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 11
125000004429 atom Chemical group 0.000 claims description 10
125000000753 cycloalkyl group Chemical group 0.000 claims description 10
125000000623 heterocyclic group Chemical group 0.000 claims description 10
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 8
SAHQDLLFHZPWGK-UHFFFAOYSA-N dodecanoic acid;silver Chemical compound [Ag].CCCCCCCCCCCC(O)=O SAHQDLLFHZPWGK-UHFFFAOYSA-N 0.000 claims description 8
239000004202 carbamide Substances 0.000 claims description 7
235000013877 carbamide Nutrition 0.000 claims description 7
229910052736 halogen Inorganic materials 0.000 claims description 7
150000002367 halogens Chemical class 0.000 claims description 7
XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 claims description 7
150000003839 salts Chemical class 0.000 claims description 7
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 6
150000001732 carboxylic acid derivatives Chemical class 0.000 claims 7
239000003638 chemical reducing agent Substances 0.000 abstract description 9
239000000758 substrate Substances 0.000 abstract description 3
239000011230 binding agent Substances 0.000 abstract 4
238000001931 thermography Methods 0.000 abstract 4
229910052709 silver Inorganic materials 0.000 description 116
239000004332 silver Substances 0.000 description 115
239000000839 emulsion Substances 0.000 description 75
230000008542 thermal sensitivity Effects 0.000 description 75
239000000243 solution Substances 0.000 description 65
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 63
238000000576 coating method Methods 0.000 description 43
239000011248 coating agent Substances 0.000 description 41
238000002360 preparation method Methods 0.000 description 28
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 27
FBSFWRHWHYMIOG-UHFFFAOYSA-N methyl 3,4,5-trihydroxybenzoate Chemical compound COC(=O)C1=CC(O)=C(O)C(O)=C1 FBSFWRHWHYMIOG-UHFFFAOYSA-N 0.000 description 22
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 21
238000007605 air drying Methods 0.000 description 19
239000003973 paint Substances 0.000 description 18
239000007787 solid Substances 0.000 description 16
239000000203 mixture Substances 0.000 description 15
229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 15
229920005989 resin Polymers 0.000 description 15
239000011347 resin Substances 0.000 description 15
230000003287 optical effect Effects 0.000 description 14
WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 12
229940081735 acetylcellulose Drugs 0.000 description 12
QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 12
229920002301 cellulose acetate Polymers 0.000 description 12
IBKQQKPQRYUGBJ-UHFFFAOYSA-N methyl gallate Natural products CC(=O)C1=CC(O)=C(O)C(O)=C1 IBKQQKPQRYUGBJ-UHFFFAOYSA-N 0.000 description 11
229920000728 polyester Polymers 0.000 description 11
RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 10
230000008569 process Effects 0.000 description 10
239000000126 substance Substances 0.000 description 10
238000005406 washing Methods 0.000 description 10
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 9
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
230000008901 benefit Effects 0.000 description 8
WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 8
238000003756 stirring Methods 0.000 description 8
238000001035 drying Methods 0.000 description 7
238000010438 heat treatment Methods 0.000 description 7
230000009467 reduction Effects 0.000 description 7
238000001228 spectrum Methods 0.000 description 7
239000002253 acid Substances 0.000 description 6
JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 6
239000012964 benzotriazole Substances 0.000 description 6
ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
CBECDWUDYQOTSW-UHFFFAOYSA-N 2-ethylbut-3-enal Chemical compound CCC(C=C)C=O CBECDWUDYQOTSW-UHFFFAOYSA-N 0.000 description 5
241001270131 Agaricus moelleri Species 0.000 description 5
230000000694 effects Effects 0.000 description 5
YAMHXTCMCPHKLN-UHFFFAOYSA-N imidazolidin-2-one Chemical compound O=C1NCCN1 YAMHXTCMCPHKLN-UHFFFAOYSA-N 0.000 description 5
229910052740 iodine Inorganic materials 0.000 description 5
JTHNLKXLWOXOQK-UHFFFAOYSA-N n-propyl vinyl ketone Natural products CCCC(=O)C=C JTHNLKXLWOXOQK-UHFFFAOYSA-N 0.000 description 5
229920002451 polyvinyl alcohol Polymers 0.000 description 5
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 4
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 4
238000013019 agitation Methods 0.000 description 4
239000000298 carbocyanine Substances 0.000 description 4
150000001721 carbon Chemical group 0.000 description 4
238000006555 catalytic reaction Methods 0.000 description 4
238000006243 chemical reaction Methods 0.000 description 4
239000003153 chemical reaction reagent Substances 0.000 description 4
239000004611 light stabiliser Substances 0.000 description 4
238000012545 processing Methods 0.000 description 4
229940079877 pyrogallol Drugs 0.000 description 4
229920002554 vinyl polymer Polymers 0.000 description 4
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
206010070834 Sensitisation Diseases 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
238000002679 ablation Methods 0.000 description 3
DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 3
125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 description 3
239000000853 adhesive Substances 0.000 description 3
230000001070 adhesive effect Effects 0.000 description 3
150000007933 aliphatic carboxylic acids Chemical class 0.000 description 3
230000008859 change Effects 0.000 description 3
238000010304 firing Methods 0.000 description 3
239000011521 glass Substances 0.000 description 3
230000001965 increasing effect Effects 0.000 description 3
239000011159 matrix material Substances 0.000 description 3
229910052751 metal Inorganic materials 0.000 description 3
239000002184 metal Substances 0.000 description 3
239000013307 optical fiber Substances 0.000 description 3
229910052760 oxygen Inorganic materials 0.000 description 3
QWYZFXLSWMXLDM-UHFFFAOYSA-M pinacyanol iodide Chemical compound [I-].C1=CC2=CC=CC=C2N(CC)C1=CC=CC1=CC=C(C=CC=C2)C2=[N+]1CC QWYZFXLSWMXLDM-UHFFFAOYSA-M 0.000 description 3
230000008313 sensitization Effects 0.000 description 3
239000000344 soap Substances 0.000 description 3
FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 3
238000001291 vacuum drying Methods 0.000 description 3
GWEHVDNNLFDJLR-UHFFFAOYSA-N 1,3-diphenylurea Chemical compound C=1C=CC=CC=1NC(=O)NC1=CC=CC=C1 GWEHVDNNLFDJLR-UHFFFAOYSA-N 0.000 description 2
CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Natural products OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
206010062717 Increased upper airway secretion Diseases 0.000 description 2
JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
ZTHYODDOHIVTJV-UHFFFAOYSA-N Propyl gallate Chemical compound CCCOC(=O)C1=CC(O)=C(O)C(O)=C1 ZTHYODDOHIVTJV-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
229920006383 Tyril Polymers 0.000 description 2
238000005299 abrasion Methods 0.000 description 2
230000001464 adherent effect Effects 0.000 description 2
235000010323 ascorbic acid Nutrition 0.000 description 2
229960005070 ascorbic acid Drugs 0.000 description 2
239000011668 ascorbic acid Substances 0.000 description 2
239000012752 auxiliary agent Substances 0.000 description 2
XYOVOXDWRFGKEX-UHFFFAOYSA-N azepine Chemical compound N1C=CC=CC=C1 XYOVOXDWRFGKEX-UHFFFAOYSA-N 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
VQLYBLABXAHUDN-UHFFFAOYSA-N bis(4-fluorophenyl)-methyl-(1,2,4-triazol-1-ylmethyl)silane;methyl n-(1h-benzimidazol-2-yl)carbamate Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1.C=1C=C(F)C=CC=1[Si](C=1C=CC(F)=CC=1)(C)CN1C=NC=N1 VQLYBLABXAHUDN-UHFFFAOYSA-N 0.000 description 2
KVNRLNFWIYMESJ-UHFFFAOYSA-N butyronitrile Chemical compound CCCC#N KVNRLNFWIYMESJ-UHFFFAOYSA-N 0.000 description 2
YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
238000007796 conventional method Methods 0.000 description 2
BGTOWKSIORTVQH-UHFFFAOYSA-N cyclopentanone Chemical compound O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 0.000 description 2
230000002950 deficient Effects 0.000 description 2
229910001873 dinitrogen Inorganic materials 0.000 description 2
238000009826 distribution Methods 0.000 description 2
UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
238000001914 filtration Methods 0.000 description 2
LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 2
FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
150000002430 hydrocarbons Chemical group 0.000 description 2
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 2
TYQCGQRIZGCHNB-JLAZNSOCSA-N l-ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(O)=C(O)C1=O TYQCGQRIZGCHNB-JLAZNSOCSA-N 0.000 description 2
238000005259 measurement Methods 0.000 description 2
150000002739 metals Chemical class 0.000 description 2
239000012299 nitrogen atmosphere Substances 0.000 description 2
KJIFKLIQANRMOU-UHFFFAOYSA-N oxidanium;4-methylbenzenesulfonate Chemical compound O.CC1=CC=C(S(O)(=O)=O)C=C1 KJIFKLIQANRMOU-UHFFFAOYSA-N 0.000 description 2
208000026435 phlegm Diseases 0.000 description 2
229910052698 phosphorus Inorganic materials 0.000 description 2
229920000515 polycarbonate Polymers 0.000 description 2
239000004417 polycarbonate Substances 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
238000007639 printing Methods 0.000 description 2
239000000047 product Substances 0.000 description 2
238000010992 reflux Methods 0.000 description 2
230000001105 regulatory effect Effects 0.000 description 2
CLDWGXZGFUNWKB-UHFFFAOYSA-M silver;benzoate Chemical compound [Ag+].[O-]C(=O)C1=CC=CC=C1 CLDWGXZGFUNWKB-UHFFFAOYSA-M 0.000 description 2
125000004964 sulfoalkyl group Chemical group 0.000 description 2
229940124530 sulfonamide Drugs 0.000 description 2
150000003672 ureas Chemical class 0.000 description 2
CVBWTNHDKVVFMI-LBPRGKRZSA-N (2s)-1-[4-[2-[6-amino-8-[(6-bromo-1,3-benzodioxol-5-yl)sulfanyl]purin-9-yl]ethyl]piperidin-1-yl]-2-hydroxypropan-1-one Chemical compound C1CN(C(=O)[C@@H](O)C)CCC1CCN1C2=NC=NC(N)=C2N=C1SC(C(=C1)Br)=CC2=C1OCO2 CVBWTNHDKVVFMI-LBPRGKRZSA-N 0.000 description 1
WXZOVYBKECUWBQ-TYYBGVCCSA-N (e)-but-2-enedioic acid;silver Chemical compound [Ag].OC(=O)\C=C\C(O)=O WXZOVYBKECUWBQ-TYYBGVCCSA-N 0.000 description 1
WXZOVYBKECUWBQ-ODZAUARKSA-N (z)-but-2-enedioic acid;silver Chemical compound [Ag].OC(=O)\C=C/C(O)=O WXZOVYBKECUWBQ-ODZAUARKSA-N 0.000 description 1
DKEHFTXMKFQFLR-KVVVOXFISA-N (z)-docos-13-enoic acid;silver Chemical compound [Ag].CCCCCCCC\C=C/CCCCCCCCCCCC(O)=O DKEHFTXMKFQFLR-KVVVOXFISA-N 0.000 description 1
PPYXHSIUKWPTDW-KVVVOXFISA-N (z)-octadec-9-enoic acid;silver Chemical compound [Ag].CCCCCCCC\C=C/CCCCCCCC(O)=O PPYXHSIUKWPTDW-KVVVOXFISA-N 0.000 description 1
SWEICGMKXPNXNU-UHFFFAOYSA-N 1,2-dihydroindazol-3-one Chemical compound C1=CC=C2C(O)=NNC2=C1 SWEICGMKXPNXNU-UHFFFAOYSA-N 0.000 description 1
VBRIOTVNSQFZKR-UHFFFAOYSA-N 1,3-benzothiazole;silver Chemical compound [Ag].C1=CC=C2SC=NC2=C1 VBRIOTVNSQFZKR-UHFFFAOYSA-N 0.000 description 1
ZWAVGZYKJNOTPX-UHFFFAOYSA-N 1,3-diethylurea Chemical compound CCNC(=O)NCC ZWAVGZYKJNOTPX-UHFFFAOYSA-N 0.000 description 1
STOQYCJHYNCPTL-UHFFFAOYSA-N 1,3-dihydrobenzimidazole-2-thione;silver Chemical compound [Ag].C1=CC=C2NC(=S)NC2=C1 STOQYCJHYNCPTL-UHFFFAOYSA-N 0.000 description 1
YNGDWRXWKFWCJY-UHFFFAOYSA-N 1,4-Dihydropyridine Chemical compound C1C=CNC=C1 YNGDWRXWKFWCJY-UHFFFAOYSA-N 0.000 description 1
TUSDEZXZIZRFGC-UHFFFAOYSA-N 1-O-galloyl-3,6-(R)-HHDP-beta-D-glucose Natural products OC1C(O2)COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC1C(O)C2OC(=O)C1=CC(O)=C(O)C(O)=C1 TUSDEZXZIZRFGC-UHFFFAOYSA-N 0.000 description 1
GGZHVNZHFYCSEV-UHFFFAOYSA-N 1-Phenyl-5-mercaptotetrazole Chemical compound SC1=NN=NN1C1=CC=CC=C1 GGZHVNZHFYCSEV-UHFFFAOYSA-N 0.000 description 1
SNTWKPAKVQFCCF-UHFFFAOYSA-N 2,3-dihydro-1h-triazole Chemical compound N1NC=CN1 SNTWKPAKVQFCCF-UHFFFAOYSA-N 0.000 description 1
SWNXYUGSHRAIIW-UHFFFAOYSA-N 2,4-dichlorobenzoic acid;silver Chemical compound [Ag].OC(=O)C1=CC=C(Cl)C=C1Cl SWNXYUGSHRAIIW-UHFFFAOYSA-N 0.000 description 1
FFRBMBIXVSCUFS-UHFFFAOYSA-N 2,4-dinitro-1-naphthol Chemical compound C1=CC=C2C(O)=C([N+]([O-])=O)C=C([N+]([O-])=O)C2=C1 FFRBMBIXVSCUFS-UHFFFAOYSA-N 0.000 description 1
QAQJMLQRFWZOBN-UHFFFAOYSA-N 2-(3,4-dihydroxy-5-oxo-2,5-dihydrofuran-2-yl)-2-hydroxyethyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(O)C1OC(=O)C(O)=C1O QAQJMLQRFWZOBN-UHFFFAOYSA-N 0.000 description 1
HXGGUXCRSMTHGE-UHFFFAOYSA-N 2-acetamidobenzoic acid silver Chemical compound [Ag].C(C)(=O)NC1=C(C(=O)O)C=CC=C1 HXGGUXCRSMTHGE-UHFFFAOYSA-N 0.000 description 1
JKFYKCYQEWQPTM-UHFFFAOYSA-N 2-azaniumyl-2-(4-fluorophenyl)acetate Chemical compound OC(=O)C(N)C1=CC=C(F)C=C1 JKFYKCYQEWQPTM-UHFFFAOYSA-N 0.000 description 1
SQMOGVSHJGWVJE-UHFFFAOYSA-N 2-methylbenzoic acid;silver Chemical compound [Ag].CC1=CC=CC=C1C(O)=O SQMOGVSHJGWVJE-UHFFFAOYSA-N 0.000 description 1
VSKJLJHPAFKHBX-UHFFFAOYSA-N 2-methylbuta-1,3-diene;styrene Chemical compound CC(=C)C=C.C=CC1=CC=CC=C1.C=CC1=CC=CC=C1 VSKJLJHPAFKHBX-UHFFFAOYSA-N 0.000 description 1
UIQPERPLCCTBGX-UHFFFAOYSA-N 2-phenylacetic acid;silver Chemical compound [Ag].OC(=O)CC1=CC=CC=C1 UIQPERPLCCTBGX-UHFFFAOYSA-N 0.000 description 1
VQLZSLWEEWSNCA-UHFFFAOYSA-N 2-phenylbenzoic acid silver Chemical compound [Ag].C1(=CC=CC=C1)C1=C(C(=O)O)C=CC=C1 VQLZSLWEEWSNCA-UHFFFAOYSA-N 0.000 description 1
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DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
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NBYLLBXLDOPANK-UHFFFAOYSA-M silver 2-carboxyphenolate hydrate Chemical compound C1=CC=C(C(=C1)C(=O)O)[O-].O.[Ag+] NBYLLBXLDOPANK-UHFFFAOYSA-M 0.000 description 1
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Images

Classifications

- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
- G03C1/494—Silver salt compositions other than silver halide emulsions; Photothermographic systems ; Thermographic systems using noble metal compounds
- G03C1/498—Photothermographic systems, e.g. dry silver
- G03C1/4989—Photothermographic systems, e.g. dry silver characterised by a thermal imaging step, with or without exposure to light, e.g. with a thermal head, using a laser
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
- G03C1/494—Silver salt compositions other than silver halide emulsions; Photothermographic systems ; Thermographic systems using noble metal compounds
- G03C1/498—Photothermographic systems, e.g. dry silver

Landscapes

Physics & Mathematics (AREA)
Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
General Physics & Mathematics (AREA)
Optics & Photonics (AREA)
Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
Heat Sensitive Colour Forming Recording (AREA)

CN95195324A 1994-09-27 1995-08-01 可采用激光的热敏元件 Pending CN1158660A (zh)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US31301194A	1994-09-27	1994-09-27
US08/313,011		1994-09-27

Publications (1)

Publication Number	Publication Date
CN1158660A true CN1158660A (zh)	1997-09-03

Family

ID=23213996

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CN95195324A Pending CN1158660A (zh)	1994-09-27	1995-08-01	可采用激光的热敏元件

Country Status (10)

Country	Link
EP (1)	EP0783726B1 (ja)
JP (1)	JPH10506339A (ja)
KR (1)	KR970706523A (ja)
CN (1)	CN1158660A (ja)
BR (1)	BR9509042A (ja)
CA (1)	CA2197469A1 (ja)
DE (1)	DE69515496T2 (ja)
IL (1)	IL115056A0 (ja)
MX (1)	MX9702044A (ja)
WO (1)	WO1996010213A1 (ja)

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CN102275399A (zh) *	2010-06-08	2011-12-14	何仁城	利用光的热敏打印的方法及其装置
CN101750870B (zh) *	2008-12-17	2012-05-30	中国科学院理化技术研究所	烟酸类化合物作为调色剂在直接热敏成像材料中的应用
CN112882335A (zh) *	2021-01-08	2021-06-01	中国乐凯集团有限公司	含银热敏成像层、热敏打印医疗胶片及其制备方法

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US5780483A (en) *	1995-02-17	1998-07-14	Smithkline Beecham Corporation	IL-8 receptor antagonists
WO1996025157A1 (en)	1995-02-17	1996-08-22	Smithkline Beecham Corporation	Il-8 receptor antagonists
GB2305509A (en) *	1995-09-19	1997-04-09	Minnesota Mining & Mfg	Heat sensitive elements
US6005008A (en) *	1996-02-16	1999-12-21	Smithkline Beecham Corporation	IL-8 receptor antagonists
US6262113B1 (en)	1996-03-20	2001-07-17	Smithkline Beecham Corporation	IL-8 receptor antagonists
US6211373B1 (en)	1996-03-20	2001-04-03	Smithkline Beecham Corporation	Phenyl urea antagonists of the IL-8 receptor
EP0809142B1 (en) *	1996-05-21	2005-08-31	Agfa-Gevaert	Production process for a thermographic recording material with improved stability and image-tone
DE69734077T2 (de)	1996-05-21	2006-06-29	Agfa-Gevaert	Herstellungsverfahren für ein thermographisches Aufzeichnungsmaterial mit erhöhter Stabilität und verbessertem Bildton
BR9709952A (pt) *	1996-06-27	1999-08-10	Smithkline Beecham Corp	Antagonistas de receptor de il-8
US6271261B1 (en)	1996-06-27	2001-08-07	Smithkline Beecham Corporation	IL-8 receptor antagonists
US5840469A (en) *	1997-05-13	1998-11-24	Imation Corp.	Gallic acid as a laser direct thermal developer
US6348308B1 (en)	1997-09-03	2002-02-19	Agfa-Gevaert	Substantially light-insensitive thermographic recording material with improved stability and image-tone
EP1006403B1 (en) *	1998-11-30	2004-10-20	Agfa-Gevaert	Use of direct thermal transparent imaging materials including an organic silver salt for producing labels
US6902880B2 (en)	2002-11-14	2005-06-07	Agfa-Gevaert	Stabilizers for use in substantially light-insensitive thermographic recording materials
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- 1995-08-01 WO PCT/US1995/009659 patent/WO1996010213A1/en not_active Application Discontinuation
- 1995-08-01 EP EP95927547A patent/EP0783726B1/en not_active Expired - Lifetime
- 1995-08-01 CA CA002197469A patent/CA2197469A1/en not_active Abandoned
- 1995-08-01 JP JP8511726A patent/JPH10506339A/ja active Pending
- 1995-08-01 DE DE69515496T patent/DE69515496T2/de not_active Expired - Fee Related
- 1995-08-01 BR BR9509042A patent/BR9509042A/pt not_active Application Discontinuation
- 1995-08-01 MX MX9702044A patent/MX9702044A/es unknown
- 1995-08-01 KR KR1019970702019A patent/KR970706523A/ko not_active Application Discontinuation
- 1995-08-24 IL IL11505695A patent/IL115056A0/xx unknown

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Also Published As

Publication number	Publication date
KR970706523A (ko)	1997-11-03
BR9509042A (pt)	1997-09-30
MX9702044A (es)	1997-06-28
WO1996010213A1 (en)	1996-04-04
EP0783726A1 (en)	1997-07-16
IL115056A0 (en)	1995-12-08
CA2197469A1 (en)	1996-04-04
DE69515496T2 (de)	2000-09-14
DE69515496D1 (en)	2000-04-13
EP0783726B1 (en)	2000-03-08
JPH10506339A (ja)	1998-06-23

Publication	Publication Date	Title
CN1158660A (zh)	1997-09-03	可采用激光的热敏元件
US4395484A (en)	1983-07-26	Roomlight-stable ultraviolet-response photothermographic imaging material
MXPA97002044A (en)	1997-06-01	Thermographic elements addressable with the
JPS5894494A (ja)	1983-06-04	記録媒体及びその記録方法
JPH09509503A (ja)	1997-09-22	写真および光熱写真物品用ハレーション防止およびアキュタンス（ａｃｕｔａｎｃｅ）物質としてのジヒドロペリミジンスクエア酸錯体染料
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EP0582144A1 (en)	1994-02-09	Laser addressable thermal recording material
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Date	Code	Title
1997-09-03	C06	Publication
1997-09-03	PB01	Publication
1998-06-10	C01	Deemed withdrawal of patent application (patent law 1993)
1998-06-10	WD01	Invention patent application deemed withdrawn after publication