JPH0314664Y2 - - Google Patents
Info
- Publication number
- JPH0314664Y2 JPH0314664Y2 JP1984188493U JP18849384U JPH0314664Y2 JP H0314664 Y2 JPH0314664 Y2 JP H0314664Y2 JP 1984188493 U JP1984188493 U JP 1984188493U JP 18849384 U JP18849384 U JP 18849384U JP H0314664 Y2 JPH0314664 Y2 JP H0314664Y2
- Authority
- JP
- Japan
- Prior art keywords
- sheet
- image
- photosensitive
- diffusion transfer
- liquid crystal
- 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.)
- Expired
Links
- 238000012546 transfer Methods 0.000 claims description 30
- 238000009792 diffusion process Methods 0.000 claims description 29
- 238000000034 method Methods 0.000 claims description 23
- 239000000463 material Substances 0.000 claims description 21
- 239000010408 film Substances 0.000 description 44
- 239000004973 liquid crystal related substance Substances 0.000 description 32
- 238000012545 processing Methods 0.000 description 24
- 239000010410 layer Substances 0.000 description 20
- 229910052709 silver Inorganic materials 0.000 description 14
- 239000004332 silver Substances 0.000 description 14
- -1 silver halide Chemical class 0.000 description 13
- 239000003795 chemical substances by application Substances 0.000 description 9
- 238000011161 development Methods 0.000 description 8
- 239000000203 mixture Substances 0.000 description 6
- 238000007639 printing Methods 0.000 description 6
- 210000004027 cell Anatomy 0.000 description 5
- 230000008859 change Effects 0.000 description 5
- 239000000975 dye Substances 0.000 description 5
- 239000003094 microcapsule Substances 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 4
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 3
- WCLNGBQPTVENHV-MKQVXYPISA-N cholesteryl nonanoate Chemical compound C([C@@H]12)C[C@]3(C)[C@@H]([C@H](C)CCCC(C)C)CC[C@H]3[C@@H]1CC=C1[C@]2(C)CC[C@H](OC(=O)CCCCCCCC)C1 WCLNGBQPTVENHV-MKQVXYPISA-N 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000002243 precursor Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- SJDMTGSQPOFVLR-UHFFFAOYSA-N [10,13-dimethyl-17-(6-methylheptan-2-yl)-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1h-cyclopenta[a]phenanthren-3-yl] tetradecanoate Chemical compound C12CCC3(C)C(C(C)CCCC(C)C)CCC3C2CC=C2C1(C)CCC(OC(=O)CCCCCCCCCCCCC)C2 SJDMTGSQPOFVLR-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 238000003776 cleavage reaction Methods 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 230000001747 exhibiting effect Effects 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 230000007017 scission Effects 0.000 description 2
- 125000006850 spacer group Chemical group 0.000 description 2
- 230000007480 spreading Effects 0.000 description 2
- 238000003892 spreading Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- XQRFASOUJIKXRE-UHFFFAOYSA-N (4-cyanophenyl) 4-butylbenzoate Chemical compound C1=CC(CCCC)=CC=C1C(=O)OC1=CC=C(C#N)C=C1 XQRFASOUJIKXRE-UHFFFAOYSA-N 0.000 description 1
- KAEZRSFWWCTVNP-UHFFFAOYSA-N (4-methoxyphenyl)-(4-methoxyphenyl)imino-oxidoazanium Chemical compound C1=CC(OC)=CC=C1N=[N+]([O-])C1=CC=C(OC)C=C1 KAEZRSFWWCTVNP-UHFFFAOYSA-N 0.000 description 1
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
- IQHSKAKXMQNYTA-UHFFFAOYSA-N 2-tridecylpyridine Chemical class CCCCCCCCCCCCCC1=CC=CC=N1 IQHSKAKXMQNYTA-UHFFFAOYSA-N 0.000 description 1
- XUGISPSHIFXEHZ-UHFFFAOYSA-N 3beta-acetoxy-cholest-5-ene Natural products C1C=C2CC(OC(C)=O)CCC2(C)C2C1C1CCC(C(C)CCCC(C)C)C1(C)CC2 XUGISPSHIFXEHZ-UHFFFAOYSA-N 0.000 description 1
- YEYCQJVCAMFWCO-UHFFFAOYSA-N 3beta-cholesteryl formate Natural products C1C=C2CC(OC=O)CCC2(C)C2C1C1CCC(C(C)CCCC(C)C)C1(C)CC2 YEYCQJVCAMFWCO-UHFFFAOYSA-N 0.000 description 1
- MOXOWUJNSDTVNT-UHFFFAOYSA-N 4-[(4-hexylphenyl)methylideneamino]benzonitrile Chemical compound C1=CC(CCCCCC)=CC=C1C=NC1=CC=C(C#N)C=C1 MOXOWUJNSDTVNT-UHFFFAOYSA-N 0.000 description 1
- VYYZMIPOAWOHAI-UHFFFAOYSA-N 5-amino-2-methoxybenzenesulfonamide Chemical compound COC1=CC=C(N)C=C1S(N)(=O)=O VYYZMIPOAWOHAI-UHFFFAOYSA-N 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 1
- ZLSLEPFVKRNFIM-UHFFFAOYSA-N COCCCCC1=C(C=CC=C1)N=[N+]([O-])C1=CC=CC=C1 Chemical compound COCCCCC1=C(C=CC=C1)N=[N+]([O-])C1=CC=CC=C1 ZLSLEPFVKRNFIM-UHFFFAOYSA-N 0.000 description 1
- 239000004986 Cholesteric liquid crystals (ChLC) Substances 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 239000004988 Nematic liquid crystal Substances 0.000 description 1
- CCORPVHYPHHRKB-NXUCFJMCSA-N O-Propionyl-cholesterin Natural products C([C@@H]12)C[C@]3(C)[C@@H]([C@H](C)CCCC(C)C)CC[C@H]3[C@@H]1CC=C1[C@]2(C)CC[C@H](OC(=O)CC)C1 CCORPVHYPHHRKB-NXUCFJMCSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004990 Smectic liquid crystal Substances 0.000 description 1
- 235000010724 Wisteria floribunda Nutrition 0.000 description 1
- FESYLMLHRKCTFF-MFLJIVHPSA-N [(3s,8s,9s,10r,13r,14s,17r)-10,13-dimethyl-17-[(2r)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1h-cyclopenta[a]phenanthren-3-yl] (e)-3-phenylprop-2-enoate Chemical compound O([C@@H]1CC2=CC[C@H]3[C@@H]4CC[C@@H]([C@]4(CC[C@@H]3[C@@]2(C)CC1)C)[C@H](C)CCCC(C)C)C(=O)\C=C\C1=CC=CC=C1 FESYLMLHRKCTFF-MFLJIVHPSA-N 0.000 description 1
- XMPIMLRYNVGZIA-CCEZHUSRSA-N [10,13-dimethyl-17-(6-methylheptan-2-yl)-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1h-cyclopenta[a]phenanthren-3-yl] [(e)-octadec-9-enyl] carbonate Chemical compound C12CCC3(C)C(C(C)CCCC(C)C)CCC3C2CC=C2C1(C)CCC(OC(=O)OCCCCCCCC/C=C/CCCCCCCC)C2 XMPIMLRYNVGZIA-CCEZHUSRSA-N 0.000 description 1
- IPBVNPXQWQGGJP-UHFFFAOYSA-N acetic acid phenyl ester Natural products CC(=O)OC1=CC=CC=C1 IPBVNPXQWQGGJP-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- 239000002390 adhesive tape Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- LFYJSSARVMHQJB-QIXNEVBVSA-N bakuchiol Chemical compound CC(C)=CCC[C@@](C)(C=C)\C=C\C1=CC=C(O)C=C1 LFYJSSARVMHQJB-QIXNEVBVSA-N 0.000 description 1
- 150000001558 benzoic acid derivatives Chemical class 0.000 description 1
- NJKOMDUNNDKEAI-UHFFFAOYSA-N beta-sitosterol Natural products CCC(CCC(C)C1CCC2(C)C3CC=C4CC(O)CCC4C3CCC12C)C(C)C NJKOMDUNNDKEAI-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 238000009529 body temperature measurement Methods 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- XUGISPSHIFXEHZ-VEVYEIKRSA-N cholesteryl acetate Chemical compound C1C=C2C[C@@H](OC(C)=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 XUGISPSHIFXEHZ-VEVYEIKRSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 210000002858 crystal cell Anatomy 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000004049 embossing Methods 0.000 description 1
- 238000003384 imaging method Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229940049953 phenylacetate Drugs 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- WSOMFYIWJSMIAP-UHFFFAOYSA-N propyl 7-heptoxy-9h-fluorene-2-carboxylate Chemical compound CCCOC(=O)C1=CC=C2C3=CC=C(OCCCCCCC)C=C3CC2=C1 WSOMFYIWJSMIAP-UHFFFAOYSA-N 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- NLQLSVXGSXCXFE-UHFFFAOYSA-N sitosterol Natural products CC=C(/CCC(C)C1CC2C3=CCC4C(C)C(O)CCC4(C)C3CCC2(C)C1)C(C)C NLQLSVXGSXCXFE-UHFFFAOYSA-N 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 239000003232 water-soluble binding agent Substances 0.000 description 1
Landscapes
- Measuring Temperature Or Quantity Of Heat (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1984188493U JPH0314664Y2 (sr) | 1984-12-12 | 1984-12-12 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1984188493U JPH0314664Y2 (sr) | 1984-12-12 | 1984-12-12 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61104450U JPS61104450U (sr) | 1986-07-03 |
| JPH0314664Y2 true JPH0314664Y2 (sr) | 1991-04-02 |
Family
ID=30745956
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1984188493U Expired JPH0314664Y2 (sr) | 1984-12-12 | 1984-12-12 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0314664Y2 (sr) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0531658Y2 (sr) * | 1987-04-15 | 1993-08-13 | ||
| JPH0531657Y2 (sr) * | 1987-04-15 | 1993-08-13 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5544371A (en) * | 1978-09-26 | 1980-03-28 | Hitachi Kiden Kogyo Ltd | Discharging method for sludge from inclined plate type sedimentation tank |
| JPS57135882A (en) * | 1973-07-02 | 1982-08-21 | Ashiyurei Batoraa Inc | Manufacture of temperature measuring composition |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5580731U (sr) * | 1978-11-29 | 1980-06-03 |
-
1984
- 1984-12-12 JP JP1984188493U patent/JPH0314664Y2/ja not_active Expired
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57135882A (en) * | 1973-07-02 | 1982-08-21 | Ashiyurei Batoraa Inc | Manufacture of temperature measuring composition |
| JPS5544371A (en) * | 1978-09-26 | 1980-03-28 | Hitachi Kiden Kogyo Ltd | Discharging method for sludge from inclined plate type sedimentation tank |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS61104450U (sr) | 1986-07-03 |
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