US1837679A - Process for the development of diazo-types - Google Patents
Process for the development of diazo-types Download PDFInfo
- Publication number
- US1837679A US1837679A US357325A US35732529A US1837679A US 1837679 A US1837679 A US 1837679A US 357325 A US357325 A US 357325A US 35732529 A US35732529 A US 35732529A US 1837679 A US1837679 A US 1837679A
- Authority
- US
- United States
- Prior art keywords
- diazo
- grams
- development
- types
- light
- 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 - Lifetime
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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
- G03C5/00—Photographic processes or agents therefor; Regeneration of such processing agents
- G03C5/18—Diazo-type processes, e.g. thermal development, or agents therefor
Definitions
- the present invention relates to a processfor the development of diazo types.
- diazo-compounds are light-sensitive and that by their aid photographic copies can be prepared.
- the diazo-compounds may be applied on a base either alone or in combination with an azo component, such as for instance, a phenol or an amine.
- an azo component such as for instance, a phenol or an amine.
- the layers thus obtained are exposed to light under a print and then developed by means of an alkali to which, when the first named method is employed, (viz. when the diazo-compound has been applied alone on the base), the azo component must be added.
- ammonia gaswhicl1 may, if desired, be moistened-has been found to be most suitable. In this way sharp pictures are obtained which are dry immediately.
- the wet process which requires an aftertreatment with an azo component could, hitherto, not be 1 adopted in practice, because it has various alkaline developing agent.
- the present invention is based on the discovery that weak alkalies,'such as borax, disodiumphosphate, 0r bicarbonate are particularly suitable for developing diazo types. Exceptionally sharp copies are obtained and developing baths remain stable for a suflicient length of time. As compared with the previous method of using ammoniacal baths the process according to the present invention offers the further advantage-that the baths are odorless. However, it only gives good results if the diazo-compounds are capable of uniting quickly with the azo component in an alkaline solution.
- diazo-compounds which are stable and bleach in the light, have proved to be most suitable, namely the diazo-com ounds of aminodiphenylamine, aminocar azol, dianisidine and of derivatives thereof and also the diazocompounds of similar amines and diamines.
- Moistening agents such as for instance saponine or compounds which act favorably upon the stability of the copies and their fastness to light, such as for instance derivatives of thiocarbonic acid, may also be added to the alkaline solutions.
- a paper prepared with the diazo-compound of amino cabazol is exposed to light under a. negative or. positive which is to be reproduced, for instance a photographic print, until the parts to which light has access, are bleached. out, that is until the contours of the picture have become yellow on a white ground.
- the paper is then moistened with a solution of 1 gram of ,8 naphthol and 1.5 grams of borax in 100 cubic centimeters of water. The picture appears at once.
- a paper prepared with the diazo-compound of brominated aminodiphenylamine is exposed to light as set forth in Example 1.
- the picture is developed with a solution of 0.5 grams of phloroglucine, 1.5 grams of borax and 2 grams of thiourea in 100 cubic centimeters of water. A brown picture appears at once upon a pure white ground.
- the development may also be carried out with a solution of 0.5 grams of phloroglucine and 2 grams of disodium phosphate in 100 cubic centimeters of water or with a solution' of 0.5 grams of resorcin, 1 gram of borax and 1 gram of disodium phosphate in 100 cubic centimeters of water or with a solution of 0.3 grams of phloroglucine, 0.2 grams of resorcin, 2 grams of thiourea, 1.3 grams of borax and 0.2 grams of sodium carbonate in 100 cubic centimeters of water.
- the development may be efiected by hand,
- the process of developing diazo types which comprises subjecting the layer prepared wjth a di'azo-compound after exposure to light to the action of a solution containing an azo dyestufi' component and borax.
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
Description
Patented Dec. 22, 1931 UNITED STATES PATENT OFFICE GERMANY, ASSIGNORS T0 KALLE & C0. AKTIENGESELLSCHAFT, OF WIESBADEN- IBIEZBRICH, GERMANY PROCESS FOR THE DEVELOPMENT 01' DIAZO-TYPES No Drawing. Application filed April 22, 1929, Serial No. 357,325, and in Germany March 24, .1928.
An application on this invention was filed in Germany, March 24, 1928.
The present invention relates to a processfor the development of diazo types.
It is known that diazo-compounds are light-sensitive and that by their aid photographic copies can be prepared. For this purpose the diazo-compounds may be applied on a base either alone or in combination with an azo component, such as for instance, a phenol or an amine. The layers thus obtained are exposed to light under a print and then developed by means of an alkali to which, when the first named method is employed, (viz. when the diazo-compound has been applied alone on the base), the azo component must be added.
When developing the layers containing the diazo-compound and azo components, ammonia gaswhicl1 may, if desired, be moistened-has been found to be most suitable. In this way sharp pictures are obtained which are dry immediately. The wet process which requires an aftertreatment with an azo component, could, hitherto, not be 1 adopted in practice, because it has various alkaline developing agent.
drawbacks. In most cases, for instance, the ground or high light of the picture was not satisfactory and besides this, the sizing of the paper was more or less attacked by the Furthermore, the alkaline developing baths were only stable for a short time. Caustic alkali solutions, and alkaline solutions of phenol or naphthol containing sodium or ammonium begin to discolor after standing for several hours, and in particular, the polyhydroxy -compounds of benzene and naphthalene which, otherwise, are very suitable for developing purposes, quickly deteriorate.
The present invention is based on the discovery that weak alkalies,'such as borax, disodiumphosphate, 0r bicarbonate are particularly suitable for developing diazo types. Exceptionally sharp copies are obtained and developing baths remain stable for a suflicient length of time. As compared with the previous method of using ammoniacal baths the process according to the present invention offers the further advantage-that the baths are odorless. However, it only gives good results if the diazo-compounds are capable of uniting quickly with the azo component in an alkaline solution. The 'followmg diazo-compounds which are stable and bleach in the light, have proved to be most suitable, namely the diazo-com ounds of aminodiphenylamine, aminocar azol, dianisidine and of derivatives thereof and also the diazocompounds of similar amines and diamines.
Moistening agents, such as for instance saponine or compounds which act favorably upon the stability of the copies and their fastness to light, such as for instance derivatives of thiocarbonic acid, may also be added to the alkaline solutions.
The following examples illustrate the invention, but they are not intended to limit it thereto, the parts being given by weight.
1. A paper prepared with the diazo-compound of amino cabazol is exposed to light under a. negative or. positive which is to be reproduced, for instance a photographic print, until the parts to which light has access, are bleached. out, that is until the contours of the picture have become yellow on a white ground. The paper is then moistened with a solution of 1 gram of ,8 naphthol and 1.5 grams of borax in 100 cubic centimeters of water. The picture appears at once.
2. A paper prepared with the diazo-compound of brominated aminodiphenylamine is exposed to light as set forth in Example 1. The picture is developed with a solution of 0.5 grams of phloroglucine, 1.5 grams of borax and 2 grams of thiourea in 100 cubic centimeters of water. A brown picture appears at once upon a pure white ground.
The development may also be carried out with a solution of 0.5 grams of phloroglucine and 2 grams of disodium phosphate in 100 cubic centimeters of water or with a solution' of 0.5 grams of resorcin, 1 gram of borax and 1 gram of disodium phosphate in 100 cubic centimeters of water or with a solution of 0.3 grams of phloroglucine, 0.2 grams of resorcin, 2 grams of thiourea, 1.3 grams of borax and 0.2 grams of sodium carbonate in 100 cubic centimeters of water.-
The development may be efiected by hand,
for instance by means of a wad of cotton wool or in the case of large sized copies by means of a suitable machine.
We claim:
The process of developing diazo types which comprises subjecting the layer prepared wjth a di'azo-compound after exposure to light to the action of a solution containing an azo dyestufi' component and borax.
10 In testimony whereof, we 'afiix our signatures.
MAXIMILIAN PAUL SCHMIDT. KARL HESSERT.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE308653X | 1928-03-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
US1837679A true US1837679A (en) | 1931-12-22 |
Family
ID=6121766
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US357325A Expired - Lifetime US1837679A (en) | 1928-03-24 | 1929-04-22 | Process for the development of diazo-types |
Country Status (3)
Country | Link |
---|---|
US (1) | US1837679A (en) |
FR (1) | FR671984A (en) |
GB (1) | GB308653A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2657137A (en) * | 1947-07-14 | 1953-10-27 | Grinten Chem L V D | Developer for the positive diazotype-process containing a borate, a polyhydroxy alcohol, and a coupler component |
US2657141A (en) * | 1947-07-14 | 1953-10-27 | Grinten Chem L V D | Diazotype developer composition containing a potassium borate and process of using same |
US2759818A (en) * | 1951-11-30 | 1956-08-21 | American Optical Corp | Photographic color process |
US3493371A (en) * | 1967-03-31 | 1970-02-03 | Agfa Gevaert Nv | Radiation-sensitive recording material |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1014963C2 (en) * | 1955-02-11 | 1958-02-20 | Hoechst Ag | Process for the production of insoluble azo dyes on native or regenerated protein fibers |
-
1929
- 1929-03-23 FR FR671984D patent/FR671984A/en not_active Expired
- 1929-03-25 GB GB9580/29A patent/GB308653A/en not_active Expired
- 1929-04-22 US US357325A patent/US1837679A/en not_active Expired - Lifetime
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2657137A (en) * | 1947-07-14 | 1953-10-27 | Grinten Chem L V D | Developer for the positive diazotype-process containing a borate, a polyhydroxy alcohol, and a coupler component |
US2657141A (en) * | 1947-07-14 | 1953-10-27 | Grinten Chem L V D | Diazotype developer composition containing a potassium borate and process of using same |
US2759818A (en) * | 1951-11-30 | 1956-08-21 | American Optical Corp | Photographic color process |
US3493371A (en) * | 1967-03-31 | 1970-02-03 | Agfa Gevaert Nv | Radiation-sensitive recording material |
Also Published As
Publication number | Publication date |
---|---|
FR671984A (en) | 1929-12-20 |
GB308653A (en) | 1930-03-13 |
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