GB629656A - Process for positive diazo-type and negative metal reproduction images and light-sensitive material therefor - Google Patents

Process for positive diazo-type and negative metal reproduction images and light-sensitive material therefor

Info

Publication number
GB629656A
GB629656A GB2745446A GB2745446A GB629656A GB 629656 A GB629656 A GB 629656A GB 2745446 A GB2745446 A GB 2745446A GB 2745446 A GB2745446 A GB 2745446A GB 629656 A GB629656 A GB 629656A
Authority
GB
United Kingdom
Prior art keywords
light
amino
hydroxy
acid
diazo
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
Application number
GB2745446A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
GAF Chemicals Corp
Original Assignee
General Aniline and Film Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by General Aniline and Film Corp filed Critical General Aniline and Film Corp
Priority to GB2745446A priority Critical patent/GB629656A/en
Publication of GB629656A publication Critical patent/GB629656A/en
Expired legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00Photosensitive materials
    • G03C1/52Compositions containing diazo compounds as photosensitive substances
    • G03C1/62Metal compounds reducible to metal

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

629,656. Photographic diazotype processes. FAIRWEATHER, H. G. C. (General Aniline & Film Corporation). Sept. 12, 1946, No. 27454. [Class 98 (ii)] A light-sensitive diazotype layer comprises a diazo compound capable of decomposing under the action of actinic light to produce a reducing agent, a coupling component which will form with the diazo compound an azo dye having high ultraviolet transmission characteristics, and a reducible non-light-sensitive salt of silver, mercury or thallium, the diazo compound being in such form that it will not react to convert the salt to a light-sensitive form. On exposure of this layer to ultra-violet light under a negative pattern and development with ammonia, an azo dye is produced in the parts protected from light and a metallic deposit in the parts exposed to the light, and the print as made is used as a transition print for production of positives on ordinary diazotype layers by exposure with ultra-violet light and ammonia development; thus a number of positives can be made from a negative without the necessity of wet-developing, washing or fixing operations. A list of diazo compounds which may be used includes 4-amino-N-ethyl- 1 - cyclohexylaminobenzene, 2.5 - diethoxy - 4 - phenylmercaptoacetylamino - 1 - aminobenzene, 4.4<SP>1</SP>-diamino-2.2<SP>1</SP>-5.5<SP>1</SP>-tetraethoxy triphenylmethane, N -benzene 1.2.3.4 - tetrahydroxy - 6 - aminoquinoline, 5 - amino - 2-methyl -N benzyl - 2.3-dihydroindole, 6 - amino - 9 - ethylhexahydro - carbazole, N-p-(aminophenyl)-morpholine, N- p - aminophenyl piperidine, N - ethyl - N - (4 - amino - 3 - methyl phenyl) - glycineamide, and 1-(p-aminophenyl)-pyrrolidene. Coupling components include 2.3-dihydroxynaphthalene, 1- amino - 8 -hydroxy - 3.6 -naphthalene disulphonic acid, 6-hydroxy naphthimidazole, R-salt, 2.3- dihydroxynaphthalene - 6 - sulphonic acid, H- acid, 2.4-dihydroxybenzaldehyde and dimethyldihydroresorcinol. Of the metal salts, silver, mercurous and thallous nitrates and sulphamates are particularly suitable. Paper, cellulose acetate foil or gelatin coated cellulose acetate foil may be used as ultra-violet light transmissive support for the layers. In eight examples the diazo compounds used are the fluoboric acid salts of diazotized p-aminodiethylaniline, p-amino-N.N-diethyl-metatoluidine or p-amino-diphenylamine; the coupling components 2.3 - dihydroxynaphthalene, 1- amino - 8 -hydroxy- 3.6-dihydroxynapbthalene, or 6-hydroxy-naphthimidazole; and the metal salts silver nitrate or sulphamate: these substances being added in various specified proportions, together with citric acid, to form the necessary coating solutions. Specification 391,677 is referred to.
GB2745446A 1946-09-12 1946-09-12 Process for positive diazo-type and negative metal reproduction images and light-sensitive material therefor Expired GB629656A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2745446A GB629656A (en) 1946-09-12 1946-09-12 Process for positive diazo-type and negative metal reproduction images and light-sensitive material therefor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2745446A GB629656A (en) 1946-09-12 1946-09-12 Process for positive diazo-type and negative metal reproduction images and light-sensitive material therefor

Publications (1)

Publication Number Publication Date
GB629656A true GB629656A (en) 1949-09-26

Family

ID=10259846

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2745446A Expired GB629656A (en) 1946-09-12 1946-09-12 Process for positive diazo-type and negative metal reproduction images and light-sensitive material therefor

Country Status (1)

Country Link
GB (1) GB629656A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2750292A (en) * 1950-05-26 1956-06-12 Hartford Nat Bank & Trust Co Process for producing colored photographic contrasts
US3007795A (en) * 1955-02-11 1961-11-07 Agfa Ag Process for the production of laterally non-reversed positive copies by heat development
US3081166A (en) * 1957-02-05 1963-03-12 Grinten Chem L V D Process for making positive diazotype copies by exposure to light of a mercury vaporlamp and light-sensitive material suited for this process

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2750292A (en) * 1950-05-26 1956-06-12 Hartford Nat Bank & Trust Co Process for producing colored photographic contrasts
US3007795A (en) * 1955-02-11 1961-11-07 Agfa Ag Process for the production of laterally non-reversed positive copies by heat development
US3081166A (en) * 1957-02-05 1963-03-12 Grinten Chem L V D Process for making positive diazotype copies by exposure to light of a mercury vaporlamp and light-sensitive material suited for this process

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