US2181941A - Photographic developer - Google Patents
Photographic developer Download PDFInfo
- Publication number
- US2181941A US2181941A US178726A US17872637A US2181941A US 2181941 A US2181941 A US 2181941A US 178726 A US178726 A US 178726A US 17872637 A US17872637 A US 17872637A US 2181941 A US2181941 A US 2181941A
- Authority
- US
- United States
- Prior art keywords
- developers
- developer
- photographic
- photographic developer
- agents
- 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
Links
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
- G03C5/26—Processes using silver-salt-containing photosensitive materials or agents therefor
- G03C5/29—Development processes or agents therefor
- G03C5/305—Additives other than developers
Definitions
- the present invention relates to photographic developers.
- alkaline developers For the development of latent photographic images, especially in halide silver emulsions, alkaline developers have long been used.
- the alkalinity of these developers consisting of a mixture of several substances normally is due to the presence of an alkali hydroxide or an alkali carbonate.
- :n being at least 1) alsoh ave a strong alkalinity and a tendency to absorb carbon dioxide. Moreover, all of these agents which are preferable for the purpose are liquid and many have a disagreeable odor and therefore are not suitable for the production of developing commercial use.
- R1 H or aralkyl or alkyl or hydroxyalkyl or p ly ydr va y
- the hydroxyl groups may be free or etherifled or esterified; internal ethers are also useful. It is necessary that the compound should'be well soluble in water.
- Such polyhydroxyalkylamines are especially amino-derivatives of the sugars and carbohydrates having 5 and 6 carbon atoms but also lower and higher homologues may be used.
- the carbon atoms combined with the hydroxyl groups may also be separated by one or more C-atoms without a hydroxyl group.
- glucamine methyl-, ethyl-, propyl-, dodecyl-glucamine, mannamine, galactamine, lactamine, fructamine, arabinamine, xylamine, 1- or v2-aminopropane diol.
- These bodies may be used in all kinds of known developers, for example rapid developers, fine grain developers, blue and brown tint developers, negative developers, positive developers, paper developers, reversal developers, and color developers used in the color development processes.
- Photographic developer comprising develop D sodium sm'fite 60 ing agents and an aliphatic hydroxyalkylamine mctamine d0 80 containing in its molecule at least one alkyl chain Potassium bromide do 2 having at least two hydroxyl groups combined "f with difierent carbon atoms.
- Photographic-developer comprising developing agents and mannamine. I I l 7 Soft workmg 3. Photographic developer. comprising develop- Water cc 1000 ing agents and lactamine.
- Photographic developer comprising developams" 15 lng agents and methylglucamine. Dry sodium sulfite do PAUE GOLDACKER. Xylamine dn GEORGMAISER. Potassium bromide do 2 ERNST SCHMITZ-HILLEBRECHT.
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEI0056606 | 1936-12-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
US2181941A true US2181941A (en) | 1939-12-05 |
Family
ID=7194393
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US178726A Expired - Lifetime US2181941A (en) | 1936-12-14 | 1937-12-08 | Photographic developer |
Country Status (5)
Country | Link |
---|---|
US (1) | US2181941A (fr) |
BE (1) | BE425071A (fr) |
CH (1) | CH201308A (fr) |
FR (1) | FR830642A (fr) |
GB (1) | GB488374A (fr) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2482546A (en) * | 1948-07-09 | 1949-09-20 | Gen Aniline & Film Corp | Phenoxyalkylamines as accelerators for photographic developers |
US5523478A (en) * | 1992-05-11 | 1996-06-04 | Albright & Wilson Limited | Carbohydrate-derived surfactants and their precursors |
-
0
- BE BE425071D patent/BE425071A/xx unknown
-
1937
- 1937-01-11 GB GB802/37A patent/GB488374A/en not_active Expired
- 1937-11-17 CH CH201308D patent/CH201308A/de unknown
- 1937-12-08 US US178726A patent/US2181941A/en not_active Expired - Lifetime
- 1937-12-10 FR FR830642D patent/FR830642A/fr not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2482546A (en) * | 1948-07-09 | 1949-09-20 | Gen Aniline & Film Corp | Phenoxyalkylamines as accelerators for photographic developers |
US5523478A (en) * | 1992-05-11 | 1996-06-04 | Albright & Wilson Limited | Carbohydrate-derived surfactants and their precursors |
US5710332A (en) * | 1992-05-11 | 1998-01-20 | Albright & Wilson Limited | Carbohydrate-derived surfactants and their precursors |
Also Published As
Publication number | Publication date |
---|---|
FR830642A (fr) | 1938-08-04 |
BE425071A (fr) | |
GB488374A (en) | 1938-07-06 |
CH201308A (de) | 1938-11-30 |
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