DE2149055A1 - Verfahren zur herstellung von druckplatten - Google Patents
Verfahren zur herstellung von druckplattenInfo
- Publication number
- DE2149055A1 DE2149055A1 DE19712149055 DE2149055A DE2149055A1 DE 2149055 A1 DE2149055 A1 DE 2149055A1 DE 19712149055 DE19712149055 DE 19712149055 DE 2149055 A DE2149055 A DE 2149055A DE 2149055 A1 DE2149055 A1 DE 2149055A1
- Authority
- DE
- Germany
- Prior art keywords
- layer
- light
- photopolymerizable
- diacetylene
- wavelength
- 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
- 238000007639 printing Methods 0.000 title claims description 34
- 238000004519 manufacturing process Methods 0.000 title claims description 18
- LLCSWKVOHICRDD-UHFFFAOYSA-N buta-1,3-diyne Chemical group C#CC#C LLCSWKVOHICRDD-UHFFFAOYSA-N 0.000 claims description 19
- 238000000034 method Methods 0.000 claims description 16
- 239000002904 solvent Substances 0.000 claims description 16
- 230000003595 spectral effect Effects 0.000 claims description 12
- 239000011230 binding agent Substances 0.000 claims description 11
- -1 diacetylene compound Chemical class 0.000 claims description 9
- 239000000725 suspension Substances 0.000 claims description 8
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 7
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 7
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims description 6
- 238000005406 washing Methods 0.000 claims description 4
- 239000000463 material Substances 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical class C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
- 125000002534 ethynyl group Chemical class [H]C#C* 0.000 claims 1
- 150000003673 urethanes Chemical class 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 description 9
- 238000006116 polymerization reaction Methods 0.000 description 9
- 239000013078 crystal Substances 0.000 description 8
- 239000003112 inhibitor Substances 0.000 description 8
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 7
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 6
- 229920001197 polyacetylene Polymers 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 150000001298 alcohols Chemical class 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 230000005855 radiation Effects 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000004202 carbamide Substances 0.000 description 3
- 125000004386 diacrylate group Chemical group 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000007669 thermal treatment Methods 0.000 description 3
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 3
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 2
- BQZJOQXSCSZQPS-UHFFFAOYSA-N 2-methoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OC)C(=O)C1=CC=CC=C1 BQZJOQXSCSZQPS-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 2
- 206010034972 Photosensitivity reaction Diseases 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000007900 aqueous suspension Substances 0.000 description 2
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 2
- 239000012876 carrier material Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 150000008049 diazo compounds Chemical group 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- 230000036211 photosensitivity Effects 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000011877 solvent mixture Substances 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-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
- CZZVAVMGKRNEAT-UHFFFAOYSA-N 2,2-dimethylpropane-1,3-diol;3-hydroxy-2,2-dimethylpropanoic acid Chemical compound OCC(C)(C)CO.OCC(C)(C)C(O)=O CZZVAVMGKRNEAT-UHFFFAOYSA-N 0.000 description 1
- TURITJIWSQEMDB-UHFFFAOYSA-N 2-methyl-n-[(2-methylprop-2-enoylamino)methyl]prop-2-enamide Chemical compound CC(=C)C(=O)NCNC(=O)C(C)=C TURITJIWSQEMDB-UHFFFAOYSA-N 0.000 description 1
- MCSXGCZMEPXKIW-UHFFFAOYSA-N 3-hydroxy-4-[(4-methyl-2-nitrophenyl)diazenyl]-N-(3-nitrophenyl)naphthalene-2-carboxamide Chemical compound Cc1ccc(N=Nc2c(O)c(cc3ccccc23)C(=O)Nc2cccc(c2)[N+]([O-])=O)c(c1)[N+]([O-])=O MCSXGCZMEPXKIW-UHFFFAOYSA-N 0.000 description 1
- JHWGFJBTMHEZME-UHFFFAOYSA-N 4-prop-2-enoyloxybutyl prop-2-enoate Chemical compound C=CC(=O)OCCCCOC(=O)C=C JHWGFJBTMHEZME-UHFFFAOYSA-N 0.000 description 1
- QSJXEFYPDANLFS-UHFFFAOYSA-N Diacetyl Chemical group CC(=O)C(C)=O QSJXEFYPDANLFS-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical class CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 1
- 244000028419 Styrax benzoin Species 0.000 description 1
- 235000000126 Styrax benzoin Nutrition 0.000 description 1
- 235000008411 Sumatra benzointree Nutrition 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 125000003118 aryl group Chemical class 0.000 description 1
- WURBFLDFSFBTLW-UHFFFAOYSA-N benzil Chemical compound C=1C=CC=CC=1C(=O)C(=O)C1=CC=CC=C1 WURBFLDFSFBTLW-UHFFFAOYSA-N 0.000 description 1
- 125000005605 benzo group Chemical group 0.000 description 1
- 229960002130 benzoin Drugs 0.000 description 1
- 230000002146 bilateral effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical class OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- VEVRNHHLCPGNDU-MUGJNUQGSA-O desmosine Chemical compound OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@H](N)C(O)=O)=C(CCC[C@H](N)C(O)=O)C(CC[C@H](N)C(O)=O)=C1 VEVRNHHLCPGNDU-MUGJNUQGSA-O 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 235000013601 eggs Nutrition 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- GVNXQWPJHHYEPC-UHFFFAOYSA-N ethyl n,n-dihexylcarbamate Chemical compound CCCCCCN(C(=O)OCC)CCCCCC GVNXQWPJHHYEPC-UHFFFAOYSA-N 0.000 description 1
- 150000002357 guanidines Chemical class 0.000 description 1
- 229940083094 guanine derivative acting on arteriolar smooth muscle Drugs 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical class CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 1
- NFMHSPWHNQRFNR-UHFFFAOYSA-N hyponitrous acid Chemical class ON=NO NFMHSPWHNQRFNR-UHFFFAOYSA-N 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 230000031700 light absorption Effects 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 150000002826 nitrites Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- UWJJYHHHVWZFEP-UHFFFAOYSA-N pentane-1,1-diol Chemical class CCCCC(O)O UWJJYHHHVWZFEP-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 238000000016 photochemical curing Methods 0.000 description 1
- 238000001782 photodegradation Methods 0.000 description 1
- 238000006303 photolysis reaction Methods 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 229920000191 poly(N-vinyl pyrrolidone) Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920005596 polymer binder Polymers 0.000 description 1
- 239000002491 polymer binding agent Substances 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical class CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical class NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 1
- 150000004053 quinones Chemical class 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 238000001429 visible spectrum Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 238000012982 x-ray structure analysis Methods 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
- G03F1/00—Originals for photomechanical production of textured or patterned surfaces, e.g., masks, photo-masks, reticles; Mask blanks or pellicles therefor; Containers specially adapted therefor; Preparation thereof
- G03F1/68—Preparation processes not covered by groups G03F1/20 - G03F1/50
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Photosensitive Polymer And Photoresist Processing (AREA)
- Printing Plates And Materials Therefor (AREA)
Priority Applications (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE789476D BE789476A (fr) | 1971-10-01 | Procede de preparation de cliches | |
| DE19712149055 DE2149055A1 (de) | 1971-10-01 | 1971-10-01 | Verfahren zur herstellung von druckplatten |
| US00290709A US3836368A (en) | 1971-10-01 | 1972-09-20 | Photopolymerizable element comprising a conjugated diacetylene layer on the photopolymer layer |
| NL7213246A NL7213246A (cg-RX-API-DMAC10.html) | 1971-10-01 | 1972-09-29 | |
| CH1428272A CH574120A5 (cg-RX-API-DMAC10.html) | 1971-10-01 | 1972-09-29 | |
| FR7234669A FR2156677B3 (cg-RX-API-DMAC10.html) | 1971-10-01 | 1972-09-29 | |
| GB4498072A GB1401790A (en) | 1971-10-01 | 1972-09-29 | Presensitised plates and their use in photopolymer printing plates |
| JP47097731A JPS4842801A (cg-RX-API-DMAC10.html) | 1971-10-01 | 1972-09-30 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19712149055 DE2149055A1 (de) | 1971-10-01 | 1971-10-01 | Verfahren zur herstellung von druckplatten |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2149055A1 true DE2149055A1 (de) | 1973-04-05 |
Family
ID=5821187
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19712149055 Pending DE2149055A1 (de) | 1971-10-01 | 1971-10-01 | Verfahren zur herstellung von druckplatten |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US3836368A (cg-RX-API-DMAC10.html) |
| JP (1) | JPS4842801A (cg-RX-API-DMAC10.html) |
| BE (1) | BE789476A (cg-RX-API-DMAC10.html) |
| CH (1) | CH574120A5 (cg-RX-API-DMAC10.html) |
| DE (1) | DE2149055A1 (cg-RX-API-DMAC10.html) |
| FR (1) | FR2156677B3 (cg-RX-API-DMAC10.html) |
| GB (1) | GB1401790A (cg-RX-API-DMAC10.html) |
| NL (1) | NL7213246A (cg-RX-API-DMAC10.html) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2821053A1 (de) * | 1977-05-17 | 1978-11-23 | Du Pont | Photohaertbares material |
| DE10028790A1 (de) * | 2000-06-15 | 2001-12-20 | Heidelberg Instruments Mikrotechnik Gmbh | Verfahren zum lithographischen Belichten von Leiterplattensubstraten |
| WO2012151033A3 (en) * | 2011-05-04 | 2013-01-03 | Eastman Kodak Company | Method for offset imaging |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4782006A (en) * | 1985-12-16 | 1988-11-01 | Canon Kabushiki Kaisha | Optical recording employing diacetylene compound and dye to form and visualize a latent image |
| US5672465A (en) * | 1990-04-09 | 1997-09-30 | Jp Laboratories, Inc. | Polyethyleneimine binder complex films |
| US5420000A (en) * | 1990-04-09 | 1995-05-30 | Jp Laboratories, Inc. | Heat fixable high energy radiation imaging film |
| US5139928A (en) * | 1990-10-23 | 1992-08-18 | Isp Investments Inc. | Imageable recording films |
| US5731112A (en) * | 1996-05-23 | 1998-03-24 | Isp Investments Inc. | Processless diacetylenic salt films capable of developing a black image |
| JPH10272750A (ja) * | 1997-03-28 | 1998-10-13 | Brother Ind Ltd | 製版用原稿シートの製造方法 |
| US9797771B2 (en) | 2013-03-21 | 2017-10-24 | Isp Investments Inc. | Diacetylene film sensitized with photoinitiator and applications of the film |
| US10782613B2 (en) | 2018-04-19 | 2020-09-22 | International Business Machines Corporation | Polymerizable self-assembled monolayers for use in atomic layer deposition |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL101499C (cg-RX-API-DMAC10.html) * | 1951-08-20 | |||
| US3451816A (en) * | 1965-06-16 | 1969-06-24 | American Cyanamid Co | Photographic dodging method |
| US3442648A (en) * | 1965-06-16 | 1969-05-06 | American Cyanamid Co | Photographic dodging method |
| US3501302A (en) * | 1966-06-06 | 1970-03-17 | Battelle Development Corp | Photosensitive polyacetylenic system and method of exposure |
| US3501308A (en) * | 1966-07-01 | 1970-03-17 | Battelle Development Corp | Photosensitive crystalline polyacetylenic sensitized with a pi-acid |
| US3723121A (en) * | 1970-11-03 | 1973-03-27 | Du Pont | Process for recording images with laser beams |
-
0
- BE BE789476D patent/BE789476A/xx unknown
-
1971
- 1971-10-01 DE DE19712149055 patent/DE2149055A1/de active Pending
-
1972
- 1972-09-20 US US00290709A patent/US3836368A/en not_active Expired - Lifetime
- 1972-09-29 FR FR7234669A patent/FR2156677B3/fr not_active Expired
- 1972-09-29 CH CH1428272A patent/CH574120A5/xx not_active IP Right Cessation
- 1972-09-29 GB GB4498072A patent/GB1401790A/en not_active Expired
- 1972-09-29 NL NL7213246A patent/NL7213246A/xx unknown
- 1972-09-30 JP JP47097731A patent/JPS4842801A/ja active Pending
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2821053A1 (de) * | 1977-05-17 | 1978-11-23 | Du Pont | Photohaertbares material |
| DE10028790A1 (de) * | 2000-06-15 | 2001-12-20 | Heidelberg Instruments Mikrotechnik Gmbh | Verfahren zum lithographischen Belichten von Leiterplattensubstraten |
| WO2012151033A3 (en) * | 2011-05-04 | 2013-01-03 | Eastman Kodak Company | Method for offset imaging |
| CN103502892A (zh) * | 2011-05-04 | 2014-01-08 | 伊斯曼柯达公司 | 用于胶印成像的方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS4842801A (cg-RX-API-DMAC10.html) | 1973-06-21 |
| CH574120A5 (cg-RX-API-DMAC10.html) | 1976-03-31 |
| FR2156677B3 (cg-RX-API-DMAC10.html) | 1975-10-17 |
| FR2156677A1 (cg-RX-API-DMAC10.html) | 1973-06-01 |
| NL7213246A (cg-RX-API-DMAC10.html) | 1973-04-03 |
| GB1401790A (en) | 1975-07-30 |
| BE789476A (fr) | 1973-03-29 |
| US3836368A (en) | 1974-09-17 |
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