CH436981A - Diazotypiematerial - Google Patents
DiazotypiematerialInfo
- Publication number
- CH436981A CH436981A CH262161A CH262161A CH436981A CH 436981 A CH436981 A CH 436981A CH 262161 A CH262161 A CH 262161A CH 262161 A CH262161 A CH 262161A CH 436981 A CH436981 A CH 436981A
- Authority
- CH
- Switzerland
- Prior art keywords
- sep
- diazo
- component
- diazotype
- compound
- Prior art date
Links
- 239000000463 material Substances 0.000 title description 13
- 150000008049 diazo compounds Chemical class 0.000 claims description 31
- -1 diazobiphenyl compound Chemical class 0.000 claims description 27
- 239000000203 mixture Substances 0.000 claims description 25
- 150000001875 compounds Chemical class 0.000 claims description 11
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 claims description 9
- 239000004305 biphenyl Substances 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 6
- 235000010290 biphenyl Nutrition 0.000 claims description 5
- 125000001424 substituent group Chemical group 0.000 claims description 5
- 125000003545 alkoxy group Chemical group 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 150000001450 anions Chemical group 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 150000001555 benzenes Chemical class 0.000 claims description 2
- 125000005805 dimethoxy phenyl group Chemical group 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000003944 tolyl group Chemical group 0.000 claims description 2
- 125000005023 xylyl group Chemical group 0.000 claims description 2
- 125000006267 biphenyl group Chemical group 0.000 claims 1
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Substances SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 claims 1
- 239000007788 liquid Substances 0.000 description 19
- 239000000987 azo dye Substances 0.000 description 17
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 12
- QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 description 9
- 229960001553 phloroglucinol Drugs 0.000 description 9
- 230000001235 sensitizing effect Effects 0.000 description 9
- 230000002378 acidificating effect Effects 0.000 description 8
- 150000003839 salts Chemical class 0.000 description 8
- JPYHHZQJCSQRJY-UHFFFAOYSA-N Phloroglucinol Natural products CCC=CCC=CCC=CCC=CCCCCC(=O)C1=C(O)C=C(O)C=C1O JPYHHZQJCSQRJY-UHFFFAOYSA-N 0.000 description 7
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 6
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000011592 zinc chloride Substances 0.000 description 6
- 235000005074 zinc chloride Nutrition 0.000 description 6
- 230000000740 bleeding effect Effects 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 230000000007 visual effect Effects 0.000 description 5
- 229910052801 chlorine Inorganic materials 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 3
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 3
- 125000001309 chloro group Chemical group Cl* 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 229920002689 polyvinyl acetate Polymers 0.000 description 3
- 239000011118 polyvinyl acetate Substances 0.000 description 3
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 3
- 239000004299 sodium benzoate Substances 0.000 description 3
- 235000010234 sodium benzoate Nutrition 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000011975 tartaric acid Substances 0.000 description 3
- 235000002906 tartaric acid Nutrition 0.000 description 3
- UECUPGFJVNJNQA-UHFFFAOYSA-N 2-phenylbenzenethiol Chemical compound SC1=CC=CC=C1C1=CC=CC=C1 UECUPGFJVNJNQA-UHFFFAOYSA-N 0.000 description 2
- 206010034972 Photosensitivity reaction Diseases 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 238000012544 monitoring process Methods 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 230000036211 photosensitivity Effects 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 229940100486 rice starch Drugs 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- VPGSXIKVUASQIY-UHFFFAOYSA-N 1,2-dibutylnaphthalene Chemical compound C1=CC=CC2=C(CCCC)C(CCCC)=CC=C21 VPGSXIKVUASQIY-UHFFFAOYSA-N 0.000 description 1
- YOOQWQDYVAVEPG-UHFFFAOYSA-N 2,5-diethoxy-4-(4-methylphenyl)-3-sulfanylbenzenediazonium;chloride Chemical compound [Cl-].CCOC1=CC([N+]#N)=C(OCC)C(S)=C1C1=CC=C(C)C=C1 YOOQWQDYVAVEPG-UHFFFAOYSA-N 0.000 description 1
- KDFHHNFGARAYMA-UHFFFAOYSA-M 2-chloro-4-(dimethylamino)-5-phenoxybenzenediazonium chloride Chemical compound [Cl-].CN(C1=C(C=C(C(=C1)Cl)[N+]#N)OC1=CC=CC=C1)C KDFHHNFGARAYMA-UHFFFAOYSA-M 0.000 description 1
- CCYLZRBAFOHVRE-UHFFFAOYSA-M 2-chloro-5-(4-chlorophenoxy)-4-(dimethylamino)benzenediazonium;chloride Chemical compound [Cl-].CN(C)C1=CC(Cl)=C([N+]#N)C=C1OC1=CC=C(Cl)C=C1 CCYLZRBAFOHVRE-UHFFFAOYSA-M 0.000 description 1
- ZXBDYBXBISDANG-UHFFFAOYSA-N 3-chloro-4-diazo-1,6-dimethyl-6-phenoxycyclohex-2-en-1-amine Chemical compound [N+](=[N-])=C1CC(C(N)(C=C1Cl)C)(C)OC1=CC=CC=C1 ZXBDYBXBISDANG-UHFFFAOYSA-N 0.000 description 1
- ZXERNCVBELBUHR-UHFFFAOYSA-N 4-(4-methylphenyl)-2,5-dipropoxy-3-sulfanylbenzenediazonium chloride Chemical compound [Cl-].CC1=CC=C(C=C1)C1=C(C(=C(C=C1OCCC)[N+]#N)OCCC)S ZXERNCVBELBUHR-UHFFFAOYSA-N 0.000 description 1
- XGWLRHNVHFNBKP-UHFFFAOYSA-N 4-diazo-2,5-dimethoxy-3-(2-methylphenyl)cyclohexa-1,5-diene-1-thiol Chemical compound [N+](=[N-])=C1C(C(=C(C=C1OC)S)OC)C1=C(C=CC=C1)C XGWLRHNVHFNBKP-UHFFFAOYSA-N 0.000 description 1
- RPJXSEWHBJOABB-UHFFFAOYSA-N 5-diazo-1,4-diethoxy-2-(4-ethoxyphenyl)cyclohexa-1,3-diene Chemical group C1=C(OCC)C(=[N+]=[N-])CC(OCC)=C1C1=CC=C(OCC)C=C1 RPJXSEWHBJOABB-UHFFFAOYSA-N 0.000 description 1
- 229910015900 BF3 Inorganic materials 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- KTMKBAIAHRMKRL-UHFFFAOYSA-N CC(CC(C(Cl)=C1)=[N+]=[N-])(C1(C)N)OC1=CC(OC)=CC=C1 Chemical compound CC(CC(C(Cl)=C1)=[N+]=[N-])(C1(C)N)OC1=CC(OC)=CC=C1 KTMKBAIAHRMKRL-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 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
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 241000220010 Rhode Species 0.000 description 1
- 239000004280 Sodium formate Substances 0.000 description 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical group [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 1
- OVKKBYSHSKKFHS-UHFFFAOYSA-N [N+](=[N-])=C1C(C(=C(C=C1OCCC)S)OCCC)C1=CC=C(C=C1)Cl Chemical compound [N+](=[N-])=C1C(C(=C(C=C1OCCC)S)OCCC)C1=CC=C(C=C1)Cl OVKKBYSHSKKFHS-UHFFFAOYSA-N 0.000 description 1
- INZHPMHKTDYNHW-UHFFFAOYSA-N [N+](=[N-])=C1CC(=C(C=C1OC)C1=C(C=CC(=C1)OC)OC)OC Chemical group [N+](=[N-])=C1CC(=C(C=C1OC)C1=C(C=CC(=C1)OC)OC)OC INZHPMHKTDYNHW-UHFFFAOYSA-N 0.000 description 1
- NHHPLVDUCRRDPO-UHFFFAOYSA-N [N+](=[N-])=C1CC(=C(C=C1OCCC)C1=CC=C(C=C1)OC)OCCC Chemical group [N+](=[N-])=C1CC(=C(C=C1OCCC)C1=CC=C(C=C1)OC)OCCC NHHPLVDUCRRDPO-UHFFFAOYSA-N 0.000 description 1
- LOMRUHZHUKRQHH-UHFFFAOYSA-N [N+](=[N-])=C1CC(=C(N(C2CCCCC2)C)C=C1Cl)OC1=CC=CC=C1 Chemical compound [N+](=[N-])=C1CC(=C(N(C2CCCCC2)C)C=C1Cl)OC1=CC=CC=C1 LOMRUHZHUKRQHH-UHFFFAOYSA-N 0.000 description 1
- KVFQOYNVFQTYJH-UHFFFAOYSA-N [N+](=[N-])=C1CC(C(N)(C=C1Cl)CC)(CC)OC1=CC=CC=C1 Chemical compound [N+](=[N-])=C1CC(C(N)(C=C1Cl)CC)(CC)OC1=CC=CC=C1 KVFQOYNVFQTYJH-UHFFFAOYSA-N 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 150000005840 aryl radicals Chemical class 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- QCOAPBRVQHMEPF-UHFFFAOYSA-N bis(2-methylpropyl) butanedioate Chemical compound CC(C)COC(=O)CCC(=O)OCC(C)C QCOAPBRVQHMEPF-UHFFFAOYSA-N 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000009474 immediate action Effects 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000010421 pencil drawing Methods 0.000 description 1
- QQBPIHBUCMDKFG-UHFFFAOYSA-N phenazopyridine hydrochloride Chemical group Cl.NC1=NC(N)=CC=C1N=NC1=CC=CC=C1 QQBPIHBUCMDKFG-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- HLBBKKJFGFRGMU-UHFFFAOYSA-M sodium formate Chemical compound [Na+].[O-]C=O HLBBKKJFGFRGMU-UHFFFAOYSA-M 0.000 description 1
- 235000019254 sodium formate Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- ZDQYSKICYIVCPN-UHFFFAOYSA-L sodium succinate (anhydrous) Chemical compound [Na+].[Na+].[O-]C(=O)CCC([O-])=O ZDQYSKICYIVCPN-UHFFFAOYSA-L 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 150000003513 tertiary aromatic amines Chemical class 0.000 description 1
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
- G03C1/52—Compositions containing diazo compounds as photosensitive substances
- G03C1/54—Diazonium salts or diazo anhydrides
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL233064 | 1958-11-10 | ||
| NL249191 | 1960-03-08 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH436981A true CH436981A (de) | 1967-05-31 |
Family
ID=19752211
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH262161A CH436981A (de) | 1958-11-10 | 1961-03-03 | Diazotypiematerial |
Country Status (6)
| Country | Link |
|---|---|
| CH (1) | CH436981A (forum.php) |
| DE (1) | DE1284292C2 (forum.php) |
| FR (1) | FR80414E (forum.php) |
| GB (1) | GB919812A (forum.php) |
| NL (2) | NL104269C (forum.php) |
| SE (1) | SE317871B (forum.php) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4343884A (en) * | 1980-12-29 | 1982-08-10 | Andrews Paper & Chemical Co., Inc. | Diazotype developing process and acidic developer with amine base salt |
-
0
- NL NL249191D patent/NL249191A/xx unknown
- NL NL104269D patent/NL104269C/xx active
-
1961
- 1961-02-28 DE DE19611284292 patent/DE1284292C2/de not_active Expired
- 1961-02-28 GB GB735961A patent/GB919812A/en not_active Expired
- 1961-03-01 SE SE218061A patent/SE317871B/xx unknown
- 1961-03-03 CH CH262161A patent/CH436981A/de unknown
- 1961-03-03 FR FR854496A patent/FR80414E/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| NL249191A (forum.php) | |
| FR80414E (fr) | 1963-04-26 |
| GB919812A (en) | 1963-02-27 |
| DE1284292B (de) | 1974-10-17 |
| NL104269C (forum.php) | |
| SE317871B (forum.php) | 1969-11-24 |
| DE1284292C2 (de) | 1974-10-17 |
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