US2649375A - Light-sensitive photographic element - Google Patents
Light-sensitive photographic element Download PDFInfo
- Publication number
- US2649375A US2649375A US192285A US19228550A US2649375A US 2649375 A US2649375 A US 2649375A US 192285 A US192285 A US 192285A US 19228550 A US19228550 A US 19228550A US 2649375 A US2649375 A US 2649375A
- Authority
- US
- United States
- Prior art keywords
- diethylamino
- cellulose ester
- photographic
- methylcoumarin
- per cent
- 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
- 229920002678 cellulose Polymers 0.000 claims description 35
- 239000000839 emulsion Substances 0.000 claims description 25
- AFYCEAFSNDLKSX-UHFFFAOYSA-N coumarin 460 Chemical compound CC1=CC(=O)OC2=CC(N(CC)CC)=CC=C21 AFYCEAFSNDLKSX-UHFFFAOYSA-N 0.000 claims description 23
- -1 SILVER HALIDE Chemical class 0.000 claims description 6
- 229920006395 saturated elastomer Polymers 0.000 claims description 5
- 229910052709 silver Inorganic materials 0.000 claims description 5
- 239000004332 silver Substances 0.000 claims description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
- 229920002301 cellulose acetate Polymers 0.000 description 18
- 150000002148 esters Chemical class 0.000 description 9
- 239000000463 material Substances 0.000 description 9
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 4
- 150000001735 carboxylic acids Chemical class 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 229910021607 Silver chloride Inorganic materials 0.000 description 3
- 230000005855 radiation Effects 0.000 description 3
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 3
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000000020 Nitrocellulose Substances 0.000 description 2
- FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 2
- SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N coumarin Chemical compound C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000007689 inspection Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920001220 nitrocellulos Polymers 0.000 description 2
- ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 2
- ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 2
- 239000011877 solvent mixture Substances 0.000 description 2
- KNKRKFALVUDBJE-UHFFFAOYSA-N 1,2-dichloropropane Chemical compound CC(Cl)CCl KNKRKFALVUDBJE-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- DQEFEBPAPFSJLV-UHFFFAOYSA-N Cellulose propionate Chemical compound CCC(=O)OCC1OC(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C1OC1C(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C(COC(=O)CC)O1 DQEFEBPAPFSJLV-UHFFFAOYSA-N 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- CODNYICXDISAEA-UHFFFAOYSA-N bromine monochloride Chemical compound BrCl CODNYICXDISAEA-UHFFFAOYSA-N 0.000 description 1
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 1
- 229920001727 cellulose butyrate Polymers 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 229920006218 cellulose propionate Polymers 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229960000956 coumarin Drugs 0.000 description 1
- 235000001671 coumarin Nutrition 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
- 230000001235 sensitizing effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
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
- G03C1/00—Photosensitive materials
- G03C1/76—Photosensitive materials characterised by the base or auxiliary layers
- G03C1/815—Photosensitive materials characterised by the base or auxiliary layers characterised by means for filtering or absorbing ultraviolet light, e.g. optical bleaching
- G03C1/8155—Organic compounds therefor
Definitions
- This invention relates to photographic elements and a method for identifying them.
- Motion picture film is ordinarily identified according to the manufacturer and type (c. g. cellu-" lose acetate or cellulose nitrate) by exposing letters or symbols photographically along the margins of the raw or unprocessed film. Upon development, these markings become visible and permit identification of the film.
- fluorescent materials can be added to the film base of photographic elements.
- Michaelis U. S. Patent 2,331,492, dated October 12 1943 describes a photographic element containing a fluorescent material, such as rhodamine, in the film base.
- the purpose of the fluorescent layer of Michaelis is to provide a source of radiant energy to cause exposure of a light-sensitive emulsion, which is not sensitive to primary radiation.
- Other patents show the use of fluorescent materials in the film base of a photographic element for the purpose of image intensification.
- the accompanying drawing shows a film base of a cellulose ester containing 7-diethylamino-4- methylcoumarin and a coating of a photographic silver halide emulsion on the film base.
- the amount of 7-diethylamino-4-methylcoumarin used in my invention is of material importance in determining the properties of the cellulose ester film base, and consequently, the photographic element comprising the cellulose ester film base.
- An amount less than 0.0001 per cent should not be used, nor should an amount in excess of 0.002 per cent be used, the amounts being based on the cellulose ester, since the advantageous results of my invention are not obtained outside this range.
- the 7 diethylamino-4-methylcoumarin can advantageously be added to a viscous solution or dope of the cellulose ester, and the composition agitated until homogeneity is accomplished.
- the 7-diethylamino-4-methylcoumarin can be. added in solid form, or in the form of a solution, which contains, for example, the same solvent present in the cellulose ester dope. After intimate mixing the solution is cast into a sheet and the solvent removed by evaporation. A film of the cellulose ester can be first formed, and a coating of '7-diethylamino-4-methylcoumarin applied to the cellulose ester layer, although I have found that a product is obtained which does not exhibit the homogeneity and.
- a film of cellulose ester can also be immersed in a solution of the I-diethylaminoi-methylcoumarm in a solvent having no dissolving power for the cellulose ester.
- Such modes of procedure are not generally to be preferred since. the amount. of 7-diethylamino-4- methylcoumarin used cannot be as systematic-ally controlled and the 7-diethylamino-a-methylcoumarin is easily removed from the film base during handling.
- Cellulose esters which can advantageously be used in my invention comprise cellulose acetate, cellulose propionate, cellulose butyrate, etc., mixed cellulose esters, such as cellulose acetate butyrate, etc.
- My invention is particularly adaptable to the use of cellulose acetate containing, for example, from 35 to 44.8 per cent acetyl.
- the particular solvent, or mixture of solvents, used in the cellulose ester dope will depend on the acyl content of the ester. For example, cellulose acetate containing from about 39 to 41 per cent acetyl can be dissolved in acetone.
- Cellulose acetate containing from about 42.5 to 44.0 per cent acetyl has been found to be especially useful in preparing the photographic elements of my invention. A range of acetyl from 43.0 to 43.5 per cent gives particularly useful results.
- the 7-diethylamino-4methy1cournarin can readily be incorporated into such esters by addition to a solution of the ester in a solvent mixture composed of 55 to 85 per cent by weight of methylene chloride, 15 to per cent by weight of methanol or ethanol, and 30 to 5 per cent by weight of ethylene chloride.
- the methylene chloride can comprise from 65 to 90 per cent by Weight of the solvent mixture.
- Cellulose acetate containing from 42.5 to 44.0 per cent by weight, and more particularly from 43.0 to 43.5 per cent by weight, of acetyl provides a film base possessing unusual resistance to tear and separation when subjected to stress or strain. (-See, for example, Fordyce et a1. U. S. Patents 2,492,977 and 2,492,978, dated January 3 19 50.)
- the accompanying drawing illustrates, schematically, a cross sectional view of a photographic element representative of those of my invention.
- the element comprises a support [0 of a cellulose ester, e. g. cellulose acetate of 43 per cent acetyl content containing less than 0.002 per cent (e. g. 0.0004 per cent) of 7-diethylamino-4-methylcoumarin and having thereon.
- a cellulose ester e. g. cellulose acetate of 43 per cent acetyl content containing less than 0.002 per cent (e. g. 0.0004 per cent) of 7-diethylamino-4-methylcoumarin and having thereon.
- the support 10 can be coated with a plurality of emulsions, for example, as shown in U. S. Patents 2,350,764, dated June 6, 1944; 2,360,214, dated October 10, 1944; 2,376,202, dated May 15, 1945; 2,391,198, dated December 18, 1945; 2,403,721, dated July 9, 1946; etc.
- S. patents are the usual gelatino-silver halide emulsions customarily used in the art of blackand-white or multi-color reproduction.
- emulsions can also consist of silver halide dispersed in other water-permeable colloidal materials, such as synthetic resins, e. g. polyvinyl alcohol, etc., cellulose ethers and esters, etc.
- Typical silver-halide emulsions include silver chloride, bromide, bromiodide, and chlorobromide types.
- the photographic silver-halide emulsions can contain the usual addenda, such as polymethine sensitizing dyes, anti-foggants, etc.
- a photographic element comprising at least one photographicvsilver halide emulsion layer and a colorless cellulose ester layer containing from 0.0001 to 0.002 per cent by weight, based on the cellulose ester, of 7-diethylamino-4-methylcoumarin, said cellulose ester being an ester of a saturated carboxylic acid containing from. 2 to 4 carbon atoms.
- a photographic element comprising at least one photographic silver halide emulsion layer and a colorless cellulose acetate layer containing from 0.0001 to 0.002 per cent by weight, based on the cellulose acetate, of 7-diethylamino-4- methylcoumarin.
- A. photographic clement comprising at least one photographic silver bromide emulsion layer and a colorless cellulose ester layer containing from 0.0001 to 0.002 per centby weight, based on the cellulose ester, of 7-diethylamino-4-methylcoumarin, said cellulose ester being an ester of a saturated carboxylic acid containing from 2 to 4 carbon atoms.
- A. photographic element comprising at leastone photographic silver chloride emulsion layer and a colorless cellulose ester layer containing from 0.0001 to 0.002 per cent by Weight, based on the cellulose ester, or 7-diethylamino-4methylcoumarin, said cellulose ester being an ester of a saturated carboxylic acid containing from 2 to 4 carbon atoms.
- a photographic element comprising at least one photographic silver bromiodide emulsion layer and a colorless cellulose ester layer containing from 0.0001 to 0.002 er cent by weight, based on the cellulose ester, of 7-diethylamino-4- methylcoumarin, said cellulose ester being an ester of a saturatedcarboxylic acid containing from 2 to 4 carbon atoms.
- a photographic element comprising at least one photographic silver chlorobromide emulsion layer and a colorless cellulose ester layer containing from 0.0001 to 0.002 per cent by weight, based on the cellulose ester, of 7-diethylamino- 4-methylcoumarin, said cellulose ester being an ester of a saturated carboxylic acid containing from 2 to 4 carbon atoms.
- a photographic element comprising at least one photographic silver bromide emulsion layer and a colorless.
- cellulose acetate layer containing from 0.00.01 to 0.002 per cent by weight, based on the cellulose acetate, of 7-diethylamino-4- methylcoumarin.
- a photographic element comprising at least one photographic silver chloride emulsion layer and a colorless cellulose acetate layer containing from 0.0001 to 0.002 per cent by Weight, based on the cellulose acetate, of 7-diethylamino-4- inethylcoumarin.
- a photographic element comprising at least one photographic silver bromiodide emulsion layer and a colorless cellulose acetate layer containing from 0.0001 to 0.002 per cent by Weight, based on the cellulose acetate, of '7-diethylamino- 4-niethylcoumarin.
- a photographic element comprising at 1 least one photographic silver chlorobromide emulsion layer and a colorless cellulose acetate layer containing from 0.0001 to 0.002 per cent by Weight, based on the cellulose acetate, of 7-cliethylamino-4methylcoumarin.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Laminated Bodies (AREA)
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BE506515D BE506515A (en, 2012) | 1950-10-26 | ||
US192285A US2649375A (en) | 1950-10-26 | 1950-10-26 | Light-sensitive photographic element |
DEE4478A DE946587C (de) | 1950-10-26 | 1951-10-19 | Photographisches Material und Verfahren zu seiner Herstellung |
GB24450/51A GB700646A (en) | 1950-10-26 | 1951-10-19 | Improvements in the identification of photographic materials |
FR1044132D FR1044132A (fr) | 1950-10-26 | 1951-10-24 | Procédé de marquage de produits photographiques et produits comportant application dudit procédé |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US192285A US2649375A (en) | 1950-10-26 | 1950-10-26 | Light-sensitive photographic element |
Publications (1)
Publication Number | Publication Date |
---|---|
US2649375A true US2649375A (en) | 1953-08-18 |
Family
ID=22709045
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US192285A Expired - Lifetime US2649375A (en) | 1950-10-26 | 1950-10-26 | Light-sensitive photographic element |
Country Status (5)
Country | Link |
---|---|
US (1) | US2649375A (en, 2012) |
BE (1) | BE506515A (en, 2012) |
DE (1) | DE946587C (en, 2012) |
FR (1) | FR1044132A (en, 2012) |
GB (1) | GB700646A (en, 2012) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1008569B (de) * | 1954-08-04 | 1957-05-16 | Ferrania Spa | Verfahren zur Unterscheidung verschiedener Typen von Rohfilmen |
US2928735A (en) * | 1958-11-05 | 1960-03-15 | Eastman Kodak Co | Photographic emulsions containing an antifoggant and antiplumming agent |
US3275828A (en) * | 1962-04-02 | 1966-09-27 | Georg S Mittelstaedt | Radiographic intensifying means |
US3282697A (en) * | 1961-10-17 | 1966-11-01 | Agfa Ag | Transparent intensifier foils for use with photographic materials for recording x-rays, gamma-rays or corpuscular rays |
US3359102A (en) * | 1963-04-05 | 1967-12-19 | Gevaert Photo Prod Nv | Optical brightening of photographic materials |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2038114A (en) * | 1931-04-14 | 1936-04-21 | Sylvania Ind Corp | Wrapping material |
US2331492A (en) * | 1938-06-13 | 1943-10-12 | Chromogen Inc | Process and material for printing photographic images |
US2334348A (en) * | 1941-06-23 | 1943-11-16 | Nat Marking Mach Co | Sunburn preventive |
US2391959A (en) * | 1944-01-12 | 1946-01-01 | Gallowhur George | Sun-bathing apparel |
US2508295A (en) * | 1945-11-08 | 1950-05-16 | Gen Aniline & Film Corp | Photographic filter layer for absorbing ultraviolet radiations |
US2511462A (en) * | 1946-06-11 | 1950-06-13 | Technicolor Motion Picture | Light-sensitive photographic element having a fluorescent layer and method of using the same |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE523120C (de) * | 1929-10-30 | 1931-04-20 | Hans Richter Dr | Fernseh-Glimmlampe |
DE667012C (de) * | 1932-10-05 | 1938-11-02 | Oskar Denzler Dr | Verfahren zur Herstellung von Sicherheitspapier, Banknoten, Dokumenten, Textilstoffen oder aehnlichen Werkstoffen mit Geheimkennzeichnung |
DE625225C (de) * | 1933-04-07 | 1936-02-06 | Hans Lewin Dr | Verfahren zur Kontraststeigerung von Roentgenbildern auf undurchsichtigen Unterlagen |
FR878823A (fr) * | 1941-02-18 | 1943-02-04 | Ig Farbenindustrie Ag | Procédé permettant d'accentuer les blancs et le pouvoir lumineux de la couleur de la surface des images photographiques |
-
0
- BE BE506515D patent/BE506515A/xx unknown
-
1950
- 1950-10-26 US US192285A patent/US2649375A/en not_active Expired - Lifetime
-
1951
- 1951-10-19 GB GB24450/51A patent/GB700646A/en not_active Expired
- 1951-10-19 DE DEE4478A patent/DE946587C/de not_active Expired
- 1951-10-24 FR FR1044132D patent/FR1044132A/fr not_active Expired
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2038114A (en) * | 1931-04-14 | 1936-04-21 | Sylvania Ind Corp | Wrapping material |
US2331492A (en) * | 1938-06-13 | 1943-10-12 | Chromogen Inc | Process and material for printing photographic images |
US2334348A (en) * | 1941-06-23 | 1943-11-16 | Nat Marking Mach Co | Sunburn preventive |
US2391959A (en) * | 1944-01-12 | 1946-01-01 | Gallowhur George | Sun-bathing apparel |
US2508295A (en) * | 1945-11-08 | 1950-05-16 | Gen Aniline & Film Corp | Photographic filter layer for absorbing ultraviolet radiations |
US2511462A (en) * | 1946-06-11 | 1950-06-13 | Technicolor Motion Picture | Light-sensitive photographic element having a fluorescent layer and method of using the same |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1008569B (de) * | 1954-08-04 | 1957-05-16 | Ferrania Spa | Verfahren zur Unterscheidung verschiedener Typen von Rohfilmen |
US2928735A (en) * | 1958-11-05 | 1960-03-15 | Eastman Kodak Co | Photographic emulsions containing an antifoggant and antiplumming agent |
US3282697A (en) * | 1961-10-17 | 1966-11-01 | Agfa Ag | Transparent intensifier foils for use with photographic materials for recording x-rays, gamma-rays or corpuscular rays |
US3275828A (en) * | 1962-04-02 | 1966-09-27 | Georg S Mittelstaedt | Radiographic intensifying means |
US3359102A (en) * | 1963-04-05 | 1967-12-19 | Gevaert Photo Prod Nv | Optical brightening of photographic materials |
Also Published As
Publication number | Publication date |
---|---|
FR1044132A (fr) | 1953-11-16 |
DE946587C (de) | 1956-08-02 |
GB700646A (en) | 1953-12-09 |
BE506515A (en, 2012) |
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