GB544702A - Manufacture of positive photographic prints - Google Patents
Manufacture of positive photographic printsInfo
- Publication number
- GB544702A GB544702A GB12810/39A GB1281039A GB544702A GB 544702 A GB544702 A GB 544702A GB 12810/39 A GB12810/39 A GB 12810/39A GB 1281039 A GB1281039 A GB 1281039A GB 544702 A GB544702 A GB 544702A
- Authority
- GB
- United Kingdom
- Prior art keywords
- sulphonate
- diazo
- aminobenzene
- ethyl
- methyl
- 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
- 238000004519 manufacturing process Methods 0.000 title 1
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 abstract 12
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 abstract 8
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 5
- 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 abstract 5
- 125000000217 alkyl group Chemical group 0.000 abstract 5
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 abstract 5
- 239000004327 boric acid Substances 0.000 abstract 5
- QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 abstract 5
- 229960001553 phloroglucinol Drugs 0.000 abstract 5
- 229910052708 sodium Inorganic materials 0.000 abstract 5
- 239000011734 sodium Substances 0.000 abstract 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 3
- ZOIORXHNWRGPMV-UHFFFAOYSA-N acetic acid;zinc Chemical compound [Zn].CC(O)=O.CC(O)=O ZOIORXHNWRGPMV-UHFFFAOYSA-N 0.000 abstract 3
- HTKFORQRBXIQHD-UHFFFAOYSA-N allylthiourea Chemical compound NC(=S)NCC=C HTKFORQRBXIQHD-UHFFFAOYSA-N 0.000 abstract 3
- 230000008878 coupling Effects 0.000 abstract 3
- 238000010168 coupling process Methods 0.000 abstract 3
- 238000005859 coupling reaction Methods 0.000 abstract 3
- 239000000463 material Substances 0.000 abstract 3
- 239000004246 zinc acetate Substances 0.000 abstract 3
- PYBSFPTVHNWRRC-UHFFFAOYSA-N 2-ethoxy-4-n,4-n-diethylbenzene-1,4-diamine Chemical compound CCOC1=CC(N(CC)CC)=CC=C1N PYBSFPTVHNWRRC-UHFFFAOYSA-N 0.000 abstract 2
- NHLAPJMCARJFOG-UHFFFAOYSA-N 3-methyl-1,4-dihydropyrazol-5-one Chemical compound CC1=NNC(=O)C1 NHLAPJMCARJFOG-UHFFFAOYSA-N 0.000 abstract 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 2
- DYRDKSSFIWVSNM-UHFFFAOYSA-N acetoacetanilide Chemical group CC(=O)CC(=O)NC1=CC=CC=C1 DYRDKSSFIWVSNM-UHFFFAOYSA-N 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 abstract 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 2
- 238000010438 heat treatment Methods 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 abstract 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 abstract 2
- SRWMQSFFRFWREA-UHFFFAOYSA-M zinc formate Chemical compound [Zn+2].[O-]C=O SRWMQSFFRFWREA-UHFFFAOYSA-M 0.000 abstract 2
- VTEBTSLPZCPJTP-UHFFFAOYSA-N 1-N-butyl-2-ethoxybenzene-1,4-diamine Chemical compound C(CCC)NC1=C(C=C(C=C1)N)OCC VTEBTSLPZCPJTP-UHFFFAOYSA-N 0.000 abstract 1
- GOHHBFSPKLRUNF-UHFFFAOYSA-N 1-[(dimethylamino)methyl]naphthalen-2-ol Chemical compound C1=CC=C2C(CN(C)C)=C(O)C=CC2=C1 GOHHBFSPKLRUNF-UHFFFAOYSA-N 0.000 abstract 1
- AHCDXLAGLYNTIA-UHFFFAOYSA-N 1-n-ethyl-2-methylbenzene-1,4-diamine Chemical compound CCNC1=CC=C(N)C=C1C AHCDXLAGLYNTIA-UHFFFAOYSA-N 0.000 abstract 1
- VPNFSZXMQLABLM-UHFFFAOYSA-N 2-(2-ethoxyanilino)ethanol Chemical compound CCOC1=CC=CC=C1NCCO VPNFSZXMQLABLM-UHFFFAOYSA-N 0.000 abstract 1
- PXABZNHUEJWLMA-UHFFFAOYSA-N 2-methoxy-4-n,4-n-dimethylbenzene-1,4-diamine Chemical compound COC1=CC(N(C)C)=CC=C1N PXABZNHUEJWLMA-UHFFFAOYSA-N 0.000 abstract 1
- LGMWBTURBRPNCJ-UHFFFAOYSA-N 4-n,4-n-diethyl-2-methoxybenzene-1,4-diamine Chemical compound CCN(CC)C1=CC=C(N)C(OC)=C1 LGMWBTURBRPNCJ-UHFFFAOYSA-N 0.000 abstract 1
- QNGVNLMMEQUVQK-UHFFFAOYSA-N 4-n,4-n-diethylbenzene-1,4-diamine Chemical compound CCN(CC)C1=CC=C(N)C=C1 QNGVNLMMEQUVQK-UHFFFAOYSA-N 0.000 abstract 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 abstract 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 abstract 1
- 150000001555 benzenes Chemical class 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 239000004202 carbamide Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- XTVVROIMIGLXTD-UHFFFAOYSA-N copper(II) nitrate Chemical compound [Cu+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O XTVVROIMIGLXTD-UHFFFAOYSA-N 0.000 abstract 1
- 150000008049 diazo compounds Chemical class 0.000 abstract 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 abstract 1
- 239000007789 gas Substances 0.000 abstract 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 abstract 1
- 229940046892 lead acetate Drugs 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- -1 methoxy, ethoxy, propoxy Chemical group 0.000 abstract 1
- 150000004780 naphthols Chemical group 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 229910052700 potassium Inorganic materials 0.000 abstract 1
- 239000011591 potassium Substances 0.000 abstract 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 abstract 1
- WBHQBSYUUJJSRZ-UHFFFAOYSA-M sodium bisulfate Chemical compound [Na+].OS([O-])(=O)=O WBHQBSYUUJJSRZ-UHFFFAOYSA-M 0.000 abstract 1
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 150000005846 sugar alcohols Polymers 0.000 abstract 1
- 239000011701 zinc Substances 0.000 abstract 1
- 229910052725 zinc Inorganic materials 0.000 abstract 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
- G03C1/56—Diazo sulfonates
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)
- Heat Sensitive Colour Forming Recording (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE213753X | 1938-12-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB544702A true GB544702A (en) | 1942-04-24 |
Family
ID=5814964
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB12810/39A Expired GB544702A (en) | 1938-12-05 | 1939-04-28 | Manufacture of positive photographic prints |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US2217189A (enrdf_load_stackoverflow) |
| BE (1) | BE437025A (enrdf_load_stackoverflow) |
| CH (1) | CH213753A (enrdf_load_stackoverflow) |
| FR (1) | FR861934A (enrdf_load_stackoverflow) |
| GB (1) | GB544702A (enrdf_load_stackoverflow) |
| NL (1) | NL51331C (enrdf_load_stackoverflow) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2680062A (en) * | 1949-07-23 | 1954-06-01 | Keuffel & Esser Co | Process for the production of azo dyestuff images |
| US2727820A (en) * | 1952-04-29 | 1955-12-20 | Gen Aniline & Film Corp | Light-sensitive diazotype layers containing carboxamides |
| US2732299A (en) * | 1952-07-22 | 1956-01-24 | Light sensitive | |
| US2789904A (en) * | 1953-09-17 | 1957-04-23 | Gen Aniline & Film Corp | Diazo print process |
| JPS4877835A (enrdf_load_stackoverflow) * | 1971-12-06 | 1973-10-19 | ||
| GB2190758A (en) * | 1986-04-25 | 1987-11-25 | Sharp Kk | A copying process using a thermosensitive recording substance |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR959577A (enrdf_load_stackoverflow) * | 1943-09-15 | 1950-03-31 | ||
| NL62542C (enrdf_load_stackoverflow) * | 1945-08-03 | |||
| BE468903A (enrdf_load_stackoverflow) * | 1945-08-18 | |||
| BE471336A (enrdf_load_stackoverflow) * | 1946-04-13 | |||
| US2529464A (en) * | 1946-09-23 | 1950-11-07 | Gen Aniline & Film Corp | Diazotype composition containing n-hydroxyethyl-m-toluidine-p-diazos |
| US2528460A (en) * | 1946-10-12 | 1950-10-31 | Gen Aniline & Film Corp | Diazotype compositions containing ethylene oxide derivatives of amino diazos |
| US2552354A (en) * | 1947-04-16 | 1951-05-08 | Gen Aniline & Film Corp | Diazotype layers containing diazos of n-(2-hydroxypropyl)-phenylenediamines |
| US2537001A (en) * | 1947-08-06 | 1951-01-02 | Gen Aniline & Film Corp | Diazotype layers having cyan acetyl amides as azo components |
| US2536398A (en) * | 1947-10-10 | 1951-01-02 | Gen Aniline & Film Corp | Pyrazolone diazotype couplers |
| US2533185A (en) * | 1947-10-22 | 1950-12-05 | Gen Aniline & Film Corp | Alkyl malonamates as azo coupling components in diazotype layers |
| FR253100A (enrdf_load_stackoverflow) * | 1947-11-26 | |||
| NL71256C (enrdf_load_stackoverflow) * | 1948-10-01 | |||
| US2691587A (en) * | 1949-07-20 | 1954-10-12 | Rca Corp | Developing of diazotype images |
| US2653091A (en) * | 1950-01-31 | 1953-09-22 | Rca Corp | Photographic diazotype composition and heat development thereof |
| US2703756A (en) * | 1951-12-12 | 1955-03-08 | Gen Aniline & Film Corp | Vesicular prints and process of making same |
| BE545042A (enrdf_load_stackoverflow) * | 1955-02-11 | |||
| NL100538C (enrdf_load_stackoverflow) * | 1958-11-10 | |||
| US3153592A (en) * | 1962-05-15 | 1964-10-20 | Dietzgen Co Eugene | Complex salt diazotype photoprinting materials |
| US3309200A (en) * | 1963-06-03 | 1967-03-14 | Itek Corp | Data reproduction process |
| US3389996A (en) * | 1964-10-15 | 1968-06-25 | Gen Aniline & Film Corp | Two-component heat developable diazotypes |
| DE2003542A1 (de) * | 1970-01-27 | 1971-08-12 | Kalle Ag | Diazotypieverfahren |
| US3713825A (en) * | 1970-04-27 | 1973-01-30 | Plastic Coating Corp | Light-activated diazography |
| DE3071196D1 (en) * | 1979-08-03 | 1985-11-28 | Toshiba Kk | Device for performing a heat-sensitive recording, heat-sensitive recording sheet, and a method for performing a heat-sensitive recording |
| JPH0688461B2 (ja) * | 1984-12-27 | 1994-11-09 | 富士写真フイルム株式会社 | 感熱記録材料 |
-
0
- BE BE437025D patent/BE437025A/xx unknown
- NL NL51331D patent/NL51331C/xx active
-
1939
- 1939-04-28 GB GB12810/39A patent/GB544702A/en not_active Expired
- 1939-11-07 CH CH213753D patent/CH213753A/de unknown
- 1939-11-27 US US306343A patent/US2217189A/en not_active Expired - Lifetime
- 1939-11-28 FR FR861934D patent/FR861934A/fr not_active Expired
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2680062A (en) * | 1949-07-23 | 1954-06-01 | Keuffel & Esser Co | Process for the production of azo dyestuff images |
| US2727820A (en) * | 1952-04-29 | 1955-12-20 | Gen Aniline & Film Corp | Light-sensitive diazotype layers containing carboxamides |
| US2732299A (en) * | 1952-07-22 | 1956-01-24 | Light sensitive | |
| US2789904A (en) * | 1953-09-17 | 1957-04-23 | Gen Aniline & Film Corp | Diazo print process |
| JPS4877835A (enrdf_load_stackoverflow) * | 1971-12-06 | 1973-10-19 | ||
| GB2190758A (en) * | 1986-04-25 | 1987-11-25 | Sharp Kk | A copying process using a thermosensitive recording substance |
Also Published As
| Publication number | Publication date |
|---|---|
| CH213753A (de) | 1941-03-15 |
| FR861934A (fr) | 1941-02-21 |
| US2217189A (en) | 1940-10-08 |
| NL51331C (enrdf_load_stackoverflow) | |
| BE437025A (enrdf_load_stackoverflow) |
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