US2017295A - Photographic developer - Google Patents

Photographic developer Download PDF

Info

Publication number
US2017295A
US2017295A US739279A US73927934A US2017295A US 2017295 A US2017295 A US 2017295A US 739279 A US739279 A US 739279A US 73927934 A US73927934 A US 73927934A US 2017295 A US2017295 A US 2017295A
Authority
US
United States
Prior art keywords
pyrogallol
photographic developer
developer
ether
photographic
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
Application number
US739279A
Inventor
Schultes Hermann
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.)
Evonik Operations GmbH
Original Assignee
Degussa GmbH
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 Degussa GmbH filed Critical Degussa GmbH
Application granted granted Critical
Publication of US2017295A publication Critical patent/US2017295A/en
Anticipated expiration legal-status Critical
Expired - Lifetime 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
    • G03C5/00Photographic processes or agents therefor; Regeneration of such processing agents
    • G03C5/26Processes using silver-salt-containing photosensitive materials or agents therefor
    • G03C5/29Development processes or agents therefor
    • G03C5/30Developers
    • 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
    • G03C5/00Photographic processes or agents therefor; Regeneration of such processing agents
    • G03C5/26Processes using silver-salt-containing photosensitive materials or agents therefor
    • G03C5/29Development processes or agents therefor
    • G03C5/30Developers
    • G03C5/3021Developers with oxydisable hydroxyl or amine groups linked to an aromatic ring

Landscapes

  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

Patented a. 15, 1935- UNITED STATES PATENT) OFFICE 2,017,295 riio'roeaarmc DEVELOPER velopers became developers could period of time.
been made to overcome the aforesaid Hermann Schiiltes,
assignor to Deutsche Golddeanstalt vormals Boessler,
Mainz-Mombach, Germany,
and Silber-Schei- FrankIort-on-the- Main, Germany, a German company No Drawing. Application Angnst 10, 1934, Serial No. 739,279. In
Germany December 8, 1933 4 Claims. (Cl. 95-88) g dark; As a result such prior not be kept very well for along Although many attempts have tage, no attempt, as far as I am aware, has been wholly satisfactory and successful when carried into practice on a. commercial and practical scale.
I have discovered a photographic developer which overcomes the aforesaid disadvantages of prior developers and which possesses many advantages.
It is an object of the invention to provide a photographic developer which is not highly sensitive to oxygen and which produces a clear, un-
faded negative.
It is also within the contemplation of the invention to provide a photographic developer which is wholly satisfactory in practical use and which is commercial and is 'capableof being manufactured on an industrial scale.
Other objects and advantages of the invention will become apparent from the following description.
According to the present discovery, it has been found that pyrogallol monomethyl ether possesses the advantages of pyrogallol as a photographic developer while at the same time being free from the disadvantage of high sensitiveness to oxygen. With the present developer, perfectly clear unfaded negatives can be produced.
It has likewise been discovered that homelogues of wrogallol monomethyl ether can also be used as photographic developers. Thus; for instance, monoethyl ether of pyrogallol or monomethyl ether of methyl pyro allol canbe' employed instead of pyrogallol monomethyl ether.
For. the
PHIPQ E of Giving those skilled in the disadvanart a better understanding brine iri viition, the r following specific and illustrative example is giv- Solution A A photographic developer is prepared with 5 about 100 parts by weight of water, about 65 parts by weight of sodium sulflte and about 1.7 parts by weight of potassium pyrosulflte. To this solution about 1.7 parts by weight of pyrogallol monomethyl ether or pyrogallol monoethyl ether are added.
Solution B A solution is made by dissolving about parts by weight of soda crystals (sodium car- 5 bonate) to about 100 parts by weight of water.
About equal volumes of Solution A, of Solution 13 and of water are mixed together to give-a developer. The recipe and the handling of the developer is essentially the same as that of pyro- 20 gallol.
It is to be observed that the present invention is a surprising discovery which could not. have been predicted by those skilled in the art. This is particularly true because prior experiments have shown that pyrogallol 1.3 dimethyl ether is practically ineffective as a developer.
Furthermore, it is to be noted that pyrogallol monomethyl ether can be easily produced by partially. demethylating the dimethyl ether according to known method. It is likewise possible to convert pyrogallol into monoethyl ether 'by treating it with dimethyl sulfate. A very good yield:1 may be obtained in this latter process.
I aim:
l. A photographic developer containing a pyrogallol monoalkyl ether.
4. A photographic developer containing mon0- -methyl' ether of methyl pyrogallol.
US739279A 1933-12-08 1934-08-10 Photographic developer Expired - Lifetime US2017295A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DED0067090 1933-12-08

Publications (1)

Publication Number Publication Date
US2017295A true US2017295A (en) 1935-10-15

Family

ID=7059637

Family Applications (1)

Application Number Title Priority Date Filing Date
US739279A Expired - Lifetime US2017295A (en) 1933-12-08 1934-08-10 Photographic developer

Country Status (2)

Country Link
US (1) US2017295A (en)
FR (1) FR781877A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3775124A (en) * 1971-06-14 1973-11-27 Fuji Photo Film Co Ltd Stabilizing method and composition for color photographic processing

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3775124A (en) * 1971-06-14 1973-11-27 Fuji Photo Film Co Ltd Stabilizing method and composition for color photographic processing

Also Published As

Publication number Publication date
FR781877A (en) 1935-05-23

Similar Documents

Publication Publication Date Title
JPS5720734A (en) Heat developing photosensitive material
CH379286A (en) Process for the production of color photographic images
US2017295A (en) Photographic developer
US2266430A (en) Etching solution
GB1045242A (en) Diazonium compounds and diazotype material
JPS55126241A (en) Developing solution for silver halide color photographic material
JPS5567747A (en) Developing solution for silver halide color photographic material
JPS57132146A (en) Method for processing color photographic material
US2234692A (en) Process of making p-nitrosophenol
US2531091A (en) N-acetonyl-pyridinium chloride as an azo coupling component in diazotypes
US2017167A (en) Photographic developer
US2843482A (en) Photographic bleach composition
CH448742A (en) Apparatus for the production of photographic copies by reflex exposure
GB991934A (en) Improved photographic developing agents
JPS57129434A (en) Formation of photographic image
GB506450A (en) Improvements in or relating to photographic bleaches
US2805265A (en) Aralkyl halide stabilizers
JPS54114241A (en) Silver halide photographic material
GB1195838A (en) A Method of Producing Photographic Images
GB1226517A (en)
US2206572A (en) Photographic toning with ferricyanides
SU107062A1 (en) The method of obtaining hexachlorocyclohexane
GB879443A (en) Bleach solutions for use in photography
SU105898A1 (en) The method of obtaining hexachlorocyclohexane
SU367405A1 (en) ALL-UNION