US2453347A - Stabilization of photographic prints with thiophenols - Google Patents
Stabilization of photographic prints with thiophenols Download PDFInfo
- Publication number
- US2453347A US2453347A US713383A US71338346A US2453347A US 2453347 A US2453347 A US 2453347A US 713383 A US713383 A US 713383A US 71338346 A US71338346 A US 71338346A US 2453347 A US2453347 A US 2453347A
- Authority
- US
- United States
- Prior art keywords
- stabilizing
- silver halide
- photographic
- silver
- image
- 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
- 230000006641 stabilisation Effects 0.000 title description 3
- 238000011105 stabilization Methods 0.000 title description 3
- 229910052709 silver Inorganic materials 0.000 description 25
- 239000004332 silver Substances 0.000 description 25
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 description 24
- -1 silver halide Chemical class 0.000 description 17
- 239000000839 emulsion Substances 0.000 description 15
- 230000000087 stabilizing effect Effects 0.000 description 14
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 11
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 9
- 239000003795 chemical substances by application Substances 0.000 description 8
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000000123 paper Substances 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- NBOMNTLFRHMDEZ-UHFFFAOYSA-N thiosalicylic acid Chemical compound OC(=O)C1=CC=CC=C1S NBOMNTLFRHMDEZ-UHFFFAOYSA-N 0.000 description 5
- 229940103494 thiosalicylic acid Drugs 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- BXAVKNRWVKUTLY-UHFFFAOYSA-N 4-sulfanylphenol Chemical compound OC1=CC=C(S)C=C1 BXAVKNRWVKUTLY-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- 229910003803 Gold(III) chloride Inorganic materials 0.000 description 2
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 2
- RJHLTVSLYWWTEF-UHFFFAOYSA-K gold trichloride Chemical compound Cl[Au](Cl)Cl RJHLTVSLYWWTEF-UHFFFAOYSA-K 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052762 osmium Inorganic materials 0.000 description 2
- SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 description 2
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical group [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- RMCCONIRBZIDTH-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)ethyl 1,3-dioxo-2-benzofuran-5-carboxylate Chemical compound CC(=C)C(=O)OCCOC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 RMCCONIRBZIDTH-UHFFFAOYSA-N 0.000 description 1
- VRVRGVPWCUEOGV-UHFFFAOYSA-N 2-aminothiophenol Chemical compound NC1=CC=CC=C1S VRVRGVPWCUEOGV-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 206010034972 Photosensitivity reaction Diseases 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229910006074 SO2NH2 Inorganic materials 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 235000011126 aluminium potassium sulphate Nutrition 0.000 description 1
- APUPEJJSWDHEBO-UHFFFAOYSA-P ammonium molybdate Chemical compound [NH4+].[NH4+].[O-][Mo]([O-])(=O)=O APUPEJJSWDHEBO-UHFFFAOYSA-P 0.000 description 1
- 229940010552 ammonium molybdate Drugs 0.000 description 1
- 235000018660 ammonium molybdate Nutrition 0.000 description 1
- 239000011609 ammonium molybdate Substances 0.000 description 1
- 239000000337 buffer salt Substances 0.000 description 1
- OIDPCXKPHYRNKH-UHFFFAOYSA-J chrome alum Chemical compound [K]OS(=O)(=O)O[Cr]1OS(=O)(=O)O1 OIDPCXKPHYRNKH-UHFFFAOYSA-J 0.000 description 1
- XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate group Chemical group [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 description 1
- 238000005562 fading Methods 0.000 description 1
- 229940015043 glyoxal Drugs 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- KSSNXJHPEFVKHY-UHFFFAOYSA-N phenol;hydrate Chemical compound O.OC1=CC=CC=C1 KSSNXJHPEFVKHY-UHFFFAOYSA-N 0.000 description 1
- CTYRPMDGLDAWRQ-UHFFFAOYSA-N phenyl hydrogen sulfate Chemical compound OS(=O)(=O)OC1=CC=CC=C1 CTYRPMDGLDAWRQ-UHFFFAOYSA-N 0.000 description 1
- 230000036211 photosensitivity Effects 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229940050271 potassium alum Drugs 0.000 description 1
- GRLPQNLYRHEGIJ-UHFFFAOYSA-J potassium aluminium sulfate Chemical compound [Al+3].[K+].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O GRLPQNLYRHEGIJ-UHFFFAOYSA-J 0.000 description 1
- ZNNZYHKDIALBAK-UHFFFAOYSA-M potassium thiocyanate Chemical compound [K+].[S-]C#N ZNNZYHKDIALBAK-UHFFFAOYSA-M 0.000 description 1
- 229940116357 potassium thiocyanate Drugs 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 230000003381 solubilizing effect Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- YWYZEGXAUVWDED-UHFFFAOYSA-N triammonium citrate Chemical compound [NH4+].[NH4+].[NH4+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O YWYZEGXAUVWDED-UHFFFAOYSA-N 0.000 description 1
- 150000003754 zirconium Chemical class 0.000 description 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
- G03C5/00—Photographic processes or agents therefor; Regeneration of such processing agents
- G03C5/26—Processes using silver-salt-containing photosensitive materials or agents therefor
- G03C5/38—Fixing; Developing-fixing; Hardening-fixing
- G03C5/39—Stabilising, i.e. fixing without washing out
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
- Y10S430/164—Rapid access processing
Definitions
- the silver photographic emulsions may be stabilized by compound p c y the stabilizing agent treating them with a solution of a thiophenol should be light-colored or transparent so that it such as thiophenol itself or a substituted thiodoes not f re with the View or p n of phenol.
- the thiophenol ma be one which conthe final image.v Solutions containing thiotain-s one or more benzene nuclei and may be hydroqilinone produce a ht yellow Silver salt substituted with groups such as -C00-H, NH while thiosalicylic acid produces a colorless sil- OH, -SH, 3031-1, -CSNH2, -SO2NH2.
- the vefsaltfollowing, compounds may, for example, b d Stabilization of a photographic print accordaccording to my invention.
- my process consists in exposing a photo- SH SH graphic paper to a negative followed by, develop- I i ment in the following solution diluted 1 part of' COOH developer to two parts of water.
- Example 1 Thiosalicylic acid grams- 30 i NHCOOH3 Ammonium citrate do 60 2-WIercapto-5mitro p-Acetaininoo-Hydroxy thio- Ammonlm hydroxide 60 benzene sulfonamirle thioplienol phenol Water liter 1 $97K?
- Hardening agents such as Formalin, glyoxal, zirconium salts, potassium alum, chrome alum, ammonium molybdate, etc., may also be incorporated in the solutions.
- Auric chloride or other chloride of a metal below silver and above osmium in the electromotive series may be added to the stabilizing bath as described-in Brice application Ser. No. 624,570, filed October 25, 1945, now Pat. No. 2,448,857, September 7, 1948, I
- my invention may be used either with positive emulsions such as are used on photographic papers or on negative film emulsions. It is generally necessary to use hardened emulsions according to my invention. Positive emulsions such as those employed on photographic papers are generally hardened and no further hardening treatment is required. However, in the case of certain negative film emulsions, the emulsion must be hardened before or during stabilizing according to my invention.
- the emulsion may be immersed in l the developing and stabilizing solutions, I prefer merely to moisten the surface of the emulsion with these solutions except in the case of films. Thus in the case of paper supports, the support does not become wet and the drying time is then greatly reduced.
- a rapid process for the formation of an image in a hardened silverhalide photographic layer which comprises exposing said layer, developing it with a silver halide developing agent to form a silver image and immediately thereafter stabilizing it by treatment with a solution of thiosalicylic acid only until the silver halide has been substantially'completely converted to a complex with thiosalicylic acid, leaving said complex in said layer and drying said stabilized image without any further treatment.
- a rapid process for the formation of an image in a hardened silver halide photographic layer which comprises exposing said layer, developing it with a silver halide developing agent to form a silver image and immediately thereafter stabilizing it by treatment with a solution of thiohydroquinone only until the silver halide has been substantially completely converted to a complex with thiohydroquinone, leaving said complex in said layer and drying said stabilized image without any further treatment.
- a rapid process for the formation of an image in a hardened silver halide photographic layer which comprises exposing said layer, de-. veloping it with a silver halide developing agent to form a silver image, and immediately thereafter stabilizing it by treatment with a thiophenol in the presence of a silver salt of a metal below silver'and above osmium inthe electromotive series and drying said stabilizedimage without any further treatment.
- a rapid process for the formation of a image in a hardened silver halide photographic layer which comprises exposing said layer, de-
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Description
Patented Nov. 9, 1948 i v UNITED STATES PATENT OFFICE STABILIZATION OF PHOTOGRAPHIC PRINTS WITH THIOPHENOLS Harold D. Russell, Rochester, N. Y., assignor to Eastman Kodak Company, Rochester, N. Y., a corporation of New Jersey No Drawing. Application November 30; 1946, Serial No. 713,383
Claims. (01. 95-88) 1 v 2 This invention relates to photography and paris exposed in the usual way and is then developed ticularly to the rapid processing of photographic in the customary silver halide developing agent. materials. If the emulsion is coated on a paper or other In Yackel U. S. application Ser. No 594,589, porous support, it is desirable to moisten the filed May 1.8, 1945, a rapid processing method is 5 surface of the emulsion with a sponge, a rubber described which involves the use of stabilizing roll or other applicator wet with developingsoluagents such as potassium thiocyanate, sodium tion so that the paper sup-port is not soaked with sulfate; thiourea, etc. The photographic prints the developing solution, are developed in' the usual way and are then After development has taken place, the excess treated with a' solution of the potassium thiodeveloping e t e r a e of t e print is cyanate or other stabilizing agent after which removed by any Convenient means Such as a they" are dried without washing. This produces Squeegee d t print is treatediwiththe thioa stable photographic print and materially rep l stabilizing 80111111011- The P11113058 0 duces the time necessary for processing the exstabilizing agent is o make e p d posed emulsion. ver halide remaining in the print substantially I have now found that exposed and develo d incapable of further photosensitivity. The silver photographic emulsions may be stabilized by compound p c y the stabilizing agent treating them with a solution of a thiophenol should be light-colored or transparent so that it such as thiophenol itself or a substituted thiodoes not f re with the View or p n of phenol. The thiophenol ma be one which conthe final image.v Solutions containing thiotain-s one or more benzene nuclei and may be hydroqilinone produce a ht yellow Silver salt substituted with groups such as -C00-H, NH while thiosalicylic acid produces a colorless sil- OH, -SH, 3031-1, -CSNH2, -SO2NH2. The vefsaltfollowing, compounds may, for example, b d Stabilization of a photographic print accordaccording to my invention. ing to my process consists in exposing a photo- SH SH graphic paper to a negative followed by, develop- I i ment in the following solution diluted 1 part of' COOH developer to two parts of water.
i Grams 3U Monomethyl-p-amino'phenol sulfate 3.1
Sodium sulfite (desiccated) 45 Thiosalicylic acid on g g g 0 mm c r ona e esicca e Thmhydmqumm Potassium bromide 1.9
Water to 1 liter.
After development for from 5 to 60 seconds,
for 5 seconds and bathed for 15 seconds to 15 minutes in the stabilizing solution, Prints treated in o-Aminothioplienol iii-Amino thiophenol this way were stable to sunlight, heat and hu- SH SH SH midity without printing-out or fading. The foll lowing examples illustrate stabilizing solutions sQ H which may be used.
Example 1 Thiosalicylic acid grams- 30 i NHCOOH3 Ammonium citrate do 60 2-WIercapto-5mitro p-Acetaininoo-Hydroxy thio- Ammonlm hydroxide 60 benzene sulfonamirle thioplienol phenol Water liter 1 $97K? SH 00 Example 2 Thiohydroquinone "grams" 10 Alcohol ml 250 Acetic acid ml 20 I Water liter 1 11 soiH Example 3 p-Mercapto thiobenzaimde p-Mercapto benzenesulfonate Ortho amino thiophenol "grams" 10 According to my invention a silver halide emul- Acetic acid ml 20 sion preferably a gelatino silver halide emulsion Water liter 1 the print is treated in an acetic acid stop bath 7 Example 4 Meta amino thiophenol grams' 10 Acetic acid ml 20 Water liter 1 The stabilizing solutions may contain one or more of the thiophenol stabilizing agents as Well as various buffer salts and solvents to help solubilizing the various compounds. Hardening agents such as Formalin, glyoxal, zirconium salts, potassium alum, chrome alum, ammonium molybdate, etc., may also be incorporated in the solutions. Auric chloride or other chloride of a metal below silver and above osmium in the electromotive series may be added to the stabilizing bath as described-in Brice application Ser. No. 624,570, filed October 25, 1945, now Pat. No. 2,448,857, September 7, 1948, I
It will be apparent that my invention may be used either with positive emulsions such as are used on photographic papers or on negative film emulsions. It is generally necessary to use hardened emulsions according to my invention. Positive emulsions such as those employed on photographic papers are generally hardened and no further hardening treatment is required. However, in the case of certain negative film emulsions, the emulsion must be hardened before or during stabilizing according to my invention.
Although the emulsion may be immersed in l the developing and stabilizing solutions, I prefer merely to moisten the surface of the emulsion with these solutions except in the case of films. Thus in the case of paper supports, the support does not become wet and the drying time is then greatly reduced.
It will be apparent from the foregoing descrip tion of my invention that all or a major part of the silver remains'in the emulsion after stabilizing treatment. This differs from the customary fixing and washing in which the intent is to remove the residual silver halide from the emulsion.
I claim: 1. A rapid process for the formation of an image in a hardened silver halide photographic layer which comprises exposing said layer, developing it-with a silver halide developing agent to form a silver image and immediately thereafter stabilizing it by treatment with a solution of a thiophenol only until the silver halide has been sub-.
stantially completely converted to a complex with said thiophenol, leaving said complex in said layer and drying said stabilized image Without any further treatment.
2. A rapid process for the formation of an image in a hardened silverhalide photographic layer which comprises exposing said layer, developing it with a silver halide developing agent to form a silver image and immediately thereafter stabilizing it by treatment with a solution of thiosalicylic acid only until the silver halide has been substantially'completely converted to a complex with thiosalicylic acid, leaving said complex in said layer and drying said stabilized image without any further treatment.
3. A rapid process for the formation of an image in a hardened silver halide photographic layer which comprises exposing said layer, developing it with a silver halide developing agent to form a silver image and immediately thereafter stabilizing it by treatment with a solution of thiohydroquinone only until the silver halide has been substantially completely converted to a complex with thiohydroquinone, leaving said complex in said layer and drying said stabilized image without any further treatment.
4. A rapid process for the formation of an image in a hardened silver halide photographic layer which comprises exposing said layer, de-. veloping it with a silver halide developing agent to form a silver image, and immediately thereafter stabilizing it by treatment with a thiophenol in the presence of a silver salt of a metal below silver'and above osmium inthe electromotive series and drying said stabilizedimage without any further treatment.
5. A rapid process for the formation of a image in a hardened silver halide photographic layer which comprises exposing said layer, de-
- veloping it with a silver halide developing agent to form a silver image and immediately thereafter stabilizing it by treatment with a thiophenol in the presence of auric chloride'and drying said stabilized image without any further treatment.
HAROLD D.'RUSSELL.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 1,356,236 Sulzberger Oct. 19, 1920 1,361,352 Sulzb'erger Dec. 7, 1920 2,377,375 Russell June 5, 1945 OTHER REFERENCES Kraft, Uber das Photochemische usw, Zeitschrift fur Wissenschaftliche Photographic usw., band 31, May 1933, pages 329 to 364, pages 342, 343, 345, 349 and 350 cited.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US713383A US2453347A (en) | 1946-11-30 | 1946-11-30 | Stabilization of photographic prints with thiophenols |
| GB31237/47A GB636981A (en) | 1946-11-30 | 1947-11-25 | Improvements in the stabilising of exposed and developed silver halide emulsion layers containing silver images |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US713383A US2453347A (en) | 1946-11-30 | 1946-11-30 | Stabilization of photographic prints with thiophenols |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2453347A true US2453347A (en) | 1948-11-09 |
Family
ID=24865921
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US713383A Expired - Lifetime US2453347A (en) | 1946-11-30 | 1946-11-30 | Stabilization of photographic prints with thiophenols |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US2453347A (en) |
| GB (1) | GB636981A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2618558A (en) * | 1949-04-12 | 1952-11-18 | Eastman Kodak Co | Photographic developers comprising an n,n - dialkyl-p-phenylenediamine and a benzenesulfonate |
| US2696439A (en) * | 1952-01-04 | 1954-12-07 | Levinos Steven | Photographic stabilization process |
| US2756151A (en) * | 1952-08-01 | 1956-07-24 | Eastman Kodak Co | Reduction of dye stain in processed photographic papers containing dyes |
| US3169992A (en) * | 1961-01-09 | 1965-02-16 | Eastman Kodak Co | Amine thiosulfate anhydrides |
| US4297429A (en) * | 1979-06-18 | 1981-10-27 | Mitsubishi Paper Mills, Ltd. | Photographic material and diffusion transfer processing solution for making printing plates and method for making printing plates |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1356236A (en) * | 1915-04-26 | 1920-10-19 | Sulzberger Nathan | Process of reducing the sensitiveness of silver compounds and products |
| US1361352A (en) * | 1914-12-10 | 1920-12-07 | Sulzberger Nathan | Process of desensitizing photo-sensitive silver compounds |
| US2377375A (en) * | 1943-12-14 | 1945-06-05 | Eastman Kodak Co | Thiosalicylic acid antifoggant |
-
1946
- 1946-11-30 US US713383A patent/US2453347A/en not_active Expired - Lifetime
-
1947
- 1947-11-25 GB GB31237/47A patent/GB636981A/en not_active Expired
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1361352A (en) * | 1914-12-10 | 1920-12-07 | Sulzberger Nathan | Process of desensitizing photo-sensitive silver compounds |
| US1356236A (en) * | 1915-04-26 | 1920-10-19 | Sulzberger Nathan | Process of reducing the sensitiveness of silver compounds and products |
| US2377375A (en) * | 1943-12-14 | 1945-06-05 | Eastman Kodak Co | Thiosalicylic acid antifoggant |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2618558A (en) * | 1949-04-12 | 1952-11-18 | Eastman Kodak Co | Photographic developers comprising an n,n - dialkyl-p-phenylenediamine and a benzenesulfonate |
| US2696439A (en) * | 1952-01-04 | 1954-12-07 | Levinos Steven | Photographic stabilization process |
| US2756151A (en) * | 1952-08-01 | 1956-07-24 | Eastman Kodak Co | Reduction of dye stain in processed photographic papers containing dyes |
| US3169992A (en) * | 1961-01-09 | 1965-02-16 | Eastman Kodak Co | Amine thiosulfate anhydrides |
| US4297429A (en) * | 1979-06-18 | 1981-10-27 | Mitsubishi Paper Mills, Ltd. | Photographic material and diffusion transfer processing solution for making printing plates and method for making printing plates |
Also Published As
| Publication number | Publication date |
|---|---|
| GB636981A (en) | 1950-05-10 |
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