JP2008515687A5 - - Google Patents
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- JP2008515687A5 JP2008515687A5 JP2007536755A JP2007536755A JP2008515687A5 JP 2008515687 A5 JP2008515687 A5 JP 2008515687A5 JP 2007536755 A JP2007536755 A JP 2007536755A JP 2007536755 A JP2007536755 A JP 2007536755A JP 2008515687 A5 JP2008515687 A5 JP 2008515687A5
- Authority
- JP
- Japan
- Prior art keywords
- component
- printing member
- top layer
- group
- lithographic
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000010410 layer Substances 0.000 claims 58
- 238000000034 method Methods 0.000 claims 48
- 238000003384 imaging method Methods 0.000 claims 38
- 239000012530 fluid Substances 0.000 claims 35
- 239000003795 chemical substances by application Substances 0.000 claims 30
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 13
- 239000004372 Polyvinyl alcohol Substances 0.000 claims 9
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 9
- -1 acrylyl Chemical group 0.000 claims 9
- 150000001875 compounds Chemical class 0.000 claims 9
- 239000000178 monomer Substances 0.000 claims 9
- 229920002401 polyacrylamide Polymers 0.000 claims 9
- 229920002451 polyvinyl alcohol Polymers 0.000 claims 9
- 239000003999 initiator Substances 0.000 claims 7
- 230000000977 initiatory effect Effects 0.000 claims 7
- 239000000203 mixture Substances 0.000 claims 7
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims 6
- 108010010803 Gelatin Proteins 0.000 claims 6
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims 6
- 229920006322 acrylamide copolymer Polymers 0.000 claims 6
- 239000012790 adhesive layer Substances 0.000 claims 6
- 239000003054 catalyst Substances 0.000 claims 6
- 229920001577 copolymer Polymers 0.000 claims 6
- 229920000159 gelatin Polymers 0.000 claims 6
- 239000008273 gelatin Substances 0.000 claims 6
- 235000019322 gelatine Nutrition 0.000 claims 6
- 235000011852 gelatine desserts Nutrition 0.000 claims 6
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 claims 6
- 229920001477 hydrophilic polymer Polymers 0.000 claims 6
- 229920000642 polymer Polymers 0.000 claims 6
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims 6
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims 6
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims 6
- WGTYBPLFGIVFAS-UHFFFAOYSA-M tetramethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)C WGTYBPLFGIVFAS-UHFFFAOYSA-M 0.000 claims 6
- 229920003169 water-soluble polymer Polymers 0.000 claims 6
- 150000001412 amines Chemical class 0.000 claims 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims 4
- 239000003963 antioxidant agent Substances 0.000 claims 4
- 230000003078 antioxidant effect Effects 0.000 claims 4
- 239000012954 diazonium Substances 0.000 claims 4
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 claims 4
- 239000003112 inhibitor Substances 0.000 claims 4
- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 claims 4
- 230000005855 radiation Effects 0.000 claims 4
- 150000003839 salts Chemical class 0.000 claims 4
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims 4
- YVXDRFYHWWPSOA-BQYQJAHWSA-N 1-methyl-4-[(e)-2-phenylethenyl]pyridin-1-ium Chemical compound C1=C[N+](C)=CC=C1\C=C\C1=CC=CC=C1 YVXDRFYHWWPSOA-BQYQJAHWSA-N 0.000 claims 3
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical group NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims 3
- XBGXXWUAOFEXMY-UHFFFAOYSA-J C(C(=O)[O-])(=O)[O-].[Mn+2].[Mn+2].C(C(=O)[O-])(=O)[O-] Chemical compound C(C(=O)[O-])(=O)[O-].[Mn+2].[Mn+2].C(C(=O)[O-])(=O)[O-] XBGXXWUAOFEXMY-UHFFFAOYSA-J 0.000 claims 3
- KWEXHDOBZQSNGR-UHFFFAOYSA-N CC(C)=O.CC(C)=O.NC(=O)C=C.NC(=O)C=C Chemical compound CC(C)=O.CC(C)=O.NC(=O)C=C.NC(=O)C=C KWEXHDOBZQSNGR-UHFFFAOYSA-N 0.000 claims 3
- 229920002134 Carboxymethyl cellulose Polymers 0.000 claims 3
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 claims 3
- 239000004354 Hydroxyethyl cellulose Substances 0.000 claims 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims 3
- 229920002845 Poly(methacrylic acid) Polymers 0.000 claims 3
- 229920002125 Sokalan® Polymers 0.000 claims 3
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical group OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims 3
- KLQWZWNTTNRVOZ-UHFFFAOYSA-M [3-(3,4-dimethyl-9-oxothioxanthen-2-yl)oxy-2-hydroxypropyl]-trimethylazanium;chloride Chemical group [Cl-].C1=CC=C2C(=O)C3=CC(OCC(O)C[N+](C)(C)C)=C(C)C(C)=C3SC2=C1 KLQWZWNTTNRVOZ-UHFFFAOYSA-M 0.000 claims 3
- GDNDOLAIOJSATB-UHFFFAOYSA-M [keto(dimethyl)sulfuraniumyl]methane;hydroxide Chemical compound [OH-].C[S+](C)(C)=O GDNDOLAIOJSATB-UHFFFAOYSA-M 0.000 claims 3
- 239000002168 alkylating agent Substances 0.000 claims 3
- 229940100198 alkylating agent Drugs 0.000 claims 3
- FMFOIJZEZINBNA-UHFFFAOYSA-K azanium cerium(3+) oxalate Chemical group [NH4+].[Ce+3].[O-]C(=O)C([O-])=O.[O-]C(=O)C([O-])=O FMFOIJZEZINBNA-UHFFFAOYSA-K 0.000 claims 3
- 239000001768 carboxy methyl cellulose Substances 0.000 claims 3
- 235000010948 carboxy methyl cellulose Nutrition 0.000 claims 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 3
- 239000008112 carboxymethyl-cellulose Substances 0.000 claims 3
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 claims 3
- YQGOJNYOYNNSMM-UHFFFAOYSA-N eosin Chemical compound [Na+].OC(=O)C1=CC=CC=C1C1=C2C=C(Br)C(=O)C(Br)=C2OC2=C(Br)C(O)=C(Br)C=C21 YQGOJNYOYNNSMM-UHFFFAOYSA-N 0.000 claims 3
- IINNWAYUJNWZRM-UHFFFAOYSA-L erythrosin B Chemical compound [Na+].[Na+].[O-]C(=O)C1=CC=CC=C1C1=C2C=C(I)C(=O)C(I)=C2OC2=C(I)C([O-])=C(I)C=C21 IINNWAYUJNWZRM-UHFFFAOYSA-L 0.000 claims 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims 3
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 claims 3
- 229920003063 hydroxymethyl cellulose Polymers 0.000 claims 3
- 229940031574 hydroxymethyl cellulose Drugs 0.000 claims 3
- 239000000463 material Substances 0.000 claims 3
- CXKWCBBOMKCUKX-UHFFFAOYSA-M methylene blue Chemical compound [Cl-].C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 CXKWCBBOMKCUKX-UHFFFAOYSA-M 0.000 claims 3
- 229960000907 methylthioninium chloride Drugs 0.000 claims 3
- ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical compound C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 claims 3
- OMNKZBIFPJNNIO-UHFFFAOYSA-N n-(2-methyl-4-oxopentan-2-yl)prop-2-enamide Chemical compound CC(=O)CC(C)(C)NC(=O)C=C OMNKZBIFPJNNIO-UHFFFAOYSA-N 0.000 claims 3
- AYGYHGXUJBFUJU-UHFFFAOYSA-N n-[2-(prop-2-enoylamino)ethyl]prop-2-enamide Chemical compound C=CC(=O)NCCNC(=O)C=C AYGYHGXUJBFUJU-UHFFFAOYSA-N 0.000 claims 3
- CHDKQNHKDMEASZ-UHFFFAOYSA-N n-prop-2-enoylprop-2-enamide Chemical compound C=CC(=O)NC(=O)C=C CHDKQNHKDMEASZ-UHFFFAOYSA-N 0.000 claims 3
- NXGWSWBWEQYMND-UHFFFAOYSA-N piperazine;prop-2-enamide Chemical compound NC(=O)C=C.NC(=O)C=C.C1CNCCN1 NXGWSWBWEQYMND-UHFFFAOYSA-N 0.000 claims 3
- 239000004584 polyacrylic acid Substances 0.000 claims 3
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 claims 3
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims 3
- 239000011347 resin Substances 0.000 claims 3
- 229920005989 resin Polymers 0.000 claims 3
- 229930187593 rose bengal Natural products 0.000 claims 3
- AZJPTIGZZTZIDR-UHFFFAOYSA-L rose bengal Chemical compound [K+].[K+].[O-]C(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C1=C2C=C(I)C(=O)C(I)=C2OC2=C(I)C([O-])=C(I)C=C21 AZJPTIGZZTZIDR-UHFFFAOYSA-L 0.000 claims 3
- 229940081623 rose bengal Drugs 0.000 claims 3
- STRXNPAVPKGJQR-UHFFFAOYSA-N rose bengal A Natural products O1C(=O)C(C(=CC=C2Cl)Cl)=C2C21C1=CC(I)=C(O)C(I)=C1OC1=C(I)C(O)=C(I)C=C21 STRXNPAVPKGJQR-UHFFFAOYSA-N 0.000 claims 3
- 238000012216 screening Methods 0.000 claims 3
- 239000002904 solvent Substances 0.000 claims 3
- 239000000758 substrate Substances 0.000 claims 3
- 150000003512 tertiary amines Chemical class 0.000 claims 3
- HADKRTWCOYPCPH-UHFFFAOYSA-M trimethylphenylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)C1=CC=CC=C1 HADKRTWCOYPCPH-UHFFFAOYSA-M 0.000 claims 3
- MDTPTXSNPBAUHX-UHFFFAOYSA-M trimethylsulfanium;hydroxide Chemical compound [OH-].C[S+](C)C MDTPTXSNPBAUHX-UHFFFAOYSA-M 0.000 claims 3
- 229920002554 vinyl polymer Polymers 0.000 claims 3
- 239000008096 xylene Substances 0.000 claims 3
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N 1,4-Benzenediol Natural products OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims 2
- 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 claims 2
- XHPWRTXYJFNZAW-OWOJBTEDSA-N 5-azido-2-[(e)-2-(4-azido-2-sulfophenyl)ethenyl]benzenesulfonic acid Chemical group OS(=O)(=O)C1=CC(N=[N+]=[N-])=CC=C1\C=C\C1=CC=C(N=[N+]=[N-])C=C1S(O)(=O)=O XHPWRTXYJFNZAW-OWOJBTEDSA-N 0.000 claims 2
- OHNKSVVCUPOUDJ-UHFFFAOYSA-N 5-nitro-1h-indene Chemical group [O-][N+](=O)C1=CC=C2CC=CC2=C1 OHNKSVVCUPOUDJ-UHFFFAOYSA-N 0.000 claims 2
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 claims 2
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 claims 2
- SFLRFPUCUXYORX-UHFFFAOYSA-L [Cl-].[Zn+2].COC1=C(C=C(C(=C1)SC1C(C=CC=C1)=[N+]=[N-])OC)C.[Cl-] Chemical compound [Cl-].[Zn+2].COC1=C(C=C(C(=C1)SC1C(C=CC=C1)=[N+]=[N-])OC)C.[Cl-] SFLRFPUCUXYORX-UHFFFAOYSA-L 0.000 claims 2
- XUXAJIZTCAEWAI-UHFFFAOYSA-L [Na+].[Na+].[O-]S(=O)(=O)c1cc(ccc1C=C1CCCC(=Cc2ccc(cc2S([O-])(=O)=O)N=[N+]=[N-])C1=O)N=[N+]=[N-] Chemical compound [Na+].[Na+].[O-]S(=O)(=O)c1cc(ccc1C=C1CCCC(=Cc2ccc(cc2S([O-])(=O)=O)N=[N+]=[N-])C1=O)N=[N+]=[N-] XUXAJIZTCAEWAI-UHFFFAOYSA-L 0.000 claims 2
- ZVJZTGBTLTUDAN-UHFFFAOYSA-N [Na].[Na].C1(CCCC1)=O Chemical group [Na].[Na].C1(CCCC1)=O ZVJZTGBTLTUDAN-UHFFFAOYSA-N 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- BGLGAKMTYHWWKW-UHFFFAOYSA-N acridine yellow Chemical compound [H+].[Cl-].CC1=C(N)C=C2N=C(C=C(C(C)=C3)N)C3=CC2=C1 BGLGAKMTYHWWKW-UHFFFAOYSA-N 0.000 claims 2
- 125000004849 alkoxymethyl group Chemical group 0.000 claims 2
- KSCQDDRPFHTIRL-UHFFFAOYSA-N auramine O Chemical compound [H+].[Cl-].C1=CC(N(C)C)=CC=C1C(=N)C1=CC=C(N(C)C)C=C1 KSCQDDRPFHTIRL-UHFFFAOYSA-N 0.000 claims 2
- 239000006229 carbon black Substances 0.000 claims 2
- 239000007859 condensation product Substances 0.000 claims 2
- 150000005690 diesters Chemical class 0.000 claims 2
- AOMZHDJXSYHPKS-UHFFFAOYSA-L disodium 4-amino-5-hydroxy-3-[(4-nitrophenyl)diazenyl]-6-phenyldiazenylnaphthalene-2,7-disulfonate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)C1=CC2=CC(S([O-])(=O)=O)=C(N=NC=3C=CC=CC=3)C(O)=C2C(N)=C1N=NC1=CC=C([N+]([O-])=O)C=C1 AOMZHDJXSYHPKS-UHFFFAOYSA-L 0.000 claims 2
- QSFSBJZVKYOPJT-UHFFFAOYSA-L disodium 5-azido-2-[5-(4-azido-2-sulfonatophenyl)-4-methyl-3-oxopenta-1,4-dienyl]benzenesulfonate Chemical compound [Na+].[Na+].CC(=Cc1ccc(cc1S([O-])(=O)=O)N=[N+]=[N-])C(=O)C=Cc1ccc(cc1S([O-])(=O)=O)N=[N+]=[N-] QSFSBJZVKYOPJT-UHFFFAOYSA-L 0.000 claims 2
- FPVGTPBMTFTMRT-UHFFFAOYSA-L disodium;2-amino-5-[(4-sulfonatophenyl)diazenyl]benzenesulfonate Chemical compound [Na+].[Na+].C1=C(S([O-])(=O)=O)C(N)=CC=C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 FPVGTPBMTFTMRT-UHFFFAOYSA-L 0.000 claims 2
- LHXSHHZTBFUYIS-UHFFFAOYSA-L disodium;5-azido-2-[[3-[(4-azido-2-sulfonatophenyl)methylidene]-2-oxocyclopentylidene]methyl]benzenesulfonate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)C1=CC(N=[N+]=[N-])=CC=C1C=C(CC1)C(=O)C1=CC1=CC=C(N=[N+]=[N-])C=C1S([O-])(=O)=O LHXSHHZTBFUYIS-UHFFFAOYSA-L 0.000 claims 2
- 239000006185 dispersion Substances 0.000 claims 2
- 229940011411 erythrosine Drugs 0.000 claims 2
- 235000012732 erythrosine Nutrition 0.000 claims 2
- 239000004174 erythrosine Substances 0.000 claims 2
- 235000019233 fast yellow AB Nutrition 0.000 claims 2
- 125000000687 hydroquinonyl group Chemical group C1(O)=C(C=C(O)C=C1)* 0.000 claims 2
- 230000005764 inhibitory process Effects 0.000 claims 2
- 125000000018 nitroso group Chemical group N(=O)* 0.000 claims 2
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 claims 2
- 230000009257 reactivity Effects 0.000 claims 2
- WYLWMAWLDZBLRN-UHFFFAOYSA-M sodium;4-[3-methyl-4-[[4-methyl-3-(phenylsulfamoyl)phenyl]diazenyl]-5-oxo-4h-pyrazol-1-yl]benzenesulfonate Chemical compound [Na+].CC1=NN(C=2C=CC(=CC=2)S([O-])(=O)=O)C(=O)C1N=NC(C=1)=CC=C(C)C=1S(=O)(=O)NC1=CC=CC=C1 WYLWMAWLDZBLRN-UHFFFAOYSA-M 0.000 claims 2
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims 2
- 239000001052 yellow pigment Substances 0.000 claims 2
- AVBBJTKSOPVDPK-UHFFFAOYSA-L zinc 5-diazo-2-phenoxycyclohexa-1,3-diene dichloride Chemical compound [Cl-].[Cl-].[Zn++].[N-]=[N+]=C1CC=C(Oc2ccccc2)C=C1 AVBBJTKSOPVDPK-UHFFFAOYSA-L 0.000 claims 2
- 230000007423 decrease Effects 0.000 claims 1
- 238000010187 selection method Methods 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US61769504P | 2004-10-12 | 2004-10-12 | |
| PCT/US2005/036243 WO2006044267A2 (en) | 2004-10-12 | 2005-10-12 | Inkjet-imageable lithographic printing members and methods of preparing and imaging them |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2008515687A JP2008515687A (ja) | 2008-05-15 |
| JP2008515687A5 true JP2008515687A5 (https=) | 2008-12-04 |
Family
ID=35658863
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007536755A Pending JP2008515687A (ja) | 2004-10-12 | 2005-10-12 | インクジェットイメージング可能な平板印刷部材並びにその製造法及びイメージング法 |
Country Status (4)
| Country | Link |
|---|---|
| US (6) | US20060160016A1 (https=) |
| EP (1) | EP1831021A2 (https=) |
| JP (1) | JP2008515687A (https=) |
| WO (1) | WO2006044267A2 (https=) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7779776B2 (en) * | 2005-07-18 | 2010-08-24 | Tessera, Inc. | Polyceramic-coated tool for applying a flowable composition |
| US8623586B2 (en) * | 2009-02-25 | 2014-01-07 | Gary Ganghui Teng | Method for on-press developable lithographic plate utilizing light-blocking material |
| US8323803B2 (en) * | 2009-04-01 | 2012-12-04 | Xerox Corporation | Imaging member |
| US20100251914A1 (en) * | 2009-04-01 | 2010-10-07 | Xerox Corporation | Imaging member |
| US20110120333A1 (en) * | 2009-11-23 | 2011-05-26 | Michael Karp | Direct inkjet imaging lithographic plates and methods for imaging the plates |
| US9421751B2 (en) | 2009-11-23 | 2016-08-23 | Vim-Technologies Ltd | Direct inkjet imaging lithographic plates, methods for imaging and pre-press treatment |
| US20120192741A1 (en) * | 2011-01-31 | 2012-08-02 | Moshe Nakash | Method for preparing lithographic printing plates |
| CN107107603B (zh) | 2015-08-26 | 2020-05-05 | 株式会社Lg化学 | 用于胶版印刷的铅版的制造方法以及用于胶版印刷的铅版 |
| WO2018019824A1 (en) | 2016-07-25 | 2018-02-01 | Sicpa Holding Sa | Multicomponent reactive inks and printing method |
| JP7114899B2 (ja) * | 2017-12-28 | 2022-08-09 | コニカミノルタ株式会社 | インク膜形成用原版、パターン形成方法、パターン膜形成方法、およびパターン膜形成装置 |
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| US3615567A (en) * | 1969-08-20 | 1971-10-26 | Du Pont | Photosensitive elements containing inorgainc halide image intensifiers |
| US3804620A (en) * | 1971-01-06 | 1974-04-16 | Xerox Corp | Method of producing planographic plates by photoelectrophoretic imaging |
| US3750314A (en) * | 1971-05-12 | 1973-08-07 | J Crawford | Sign holder and assembly |
| US4072528A (en) * | 1972-09-27 | 1978-02-07 | E. I. Du Pont De Nemours And Company | Oxygen barrier layers for photopolymerizable elements |
| US3891439A (en) * | 1972-11-02 | 1975-06-24 | Polychrome Corp | Aqueous developing composition for lithographic diazo printing plates |
| DE2402179C2 (de) | 1973-01-18 | 1983-03-31 | E.I. du Pont de Nemours and Co., 19898 Wilmington, Del. | Photopolymerisierbare Massen enthaltend dimere Nitrosoverbindungen |
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-
2005
- 2005-10-11 US US11/249,168 patent/US20060160016A1/en not_active Abandoned
- 2005-10-11 US US11/249,169 patent/US20060150847A1/en not_active Abandoned
- 2005-10-12 EP EP05806402A patent/EP1831021A2/en not_active Withdrawn
- 2005-10-12 WO PCT/US2005/036243 patent/WO2006044267A2/en not_active Ceased
- 2005-10-12 US US11/249,033 patent/US20060156939A1/en not_active Abandoned
- 2005-10-12 US US11/249,166 patent/US7608388B2/en not_active Expired - Fee Related
- 2005-10-12 JP JP2007536755A patent/JP2008515687A/ja active Pending
-
2009
- 2009-01-14 US US12/353,473 patent/US20090123872A1/en not_active Abandoned
-
2011
- 2011-11-18 US US13/299,569 patent/US20120060710A1/en not_active Abandoned
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