US2541472A - Direct positive emulsion containing desensitizing dye - Google Patents
Direct positive emulsion containing desensitizing dye Download PDFInfo
- Publication number
- US2541472A US2541472A US35987A US3598748A US2541472A US 2541472 A US2541472 A US 2541472A US 35987 A US35987 A US 35987A US 3598748 A US3598748 A US 3598748A US 2541472 A US2541472 A US 2541472A
- Authority
- US
- United States
- Prior art keywords
- emulsion
- direct positive
- emulsion containing
- silver chloride
- quinoline
- 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
- 239000000839 emulsion Substances 0.000 title claims description 55
- 229910021607 Silver chloride Inorganic materials 0.000 claims description 15
- 150000001875 compounds Chemical class 0.000 claims description 15
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 claims description 15
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 claims description 12
- -1 NITRO GROUP Chemical group 0.000 claims description 11
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims description 10
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 claims description 10
- 150000003839 salts Chemical group 0.000 claims description 8
- 239000012964 benzotriazole Substances 0.000 claims description 4
- KIWUVOGUEXMXSV-UHFFFAOYSA-N rhodanine Chemical class O=C1CSC(=S)N1 KIWUVOGUEXMXSV-UHFFFAOYSA-N 0.000 claims description 4
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 claims description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical class C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 1
- 108010010803 Gelatin Proteins 0.000 description 6
- 229920000159 gelatin Polymers 0.000 description 6
- 239000008273 gelatin Substances 0.000 description 6
- 235000019322 gelatine Nutrition 0.000 description 6
- 235000011852 gelatine desserts Nutrition 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 5
- 230000001376 precipitating effect Effects 0.000 description 5
- 239000000975 dye Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 4
- 150000001555 benzenes Chemical class 0.000 description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 3
- ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 2
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 2
- 229910001961 silver nitrate Inorganic materials 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- SYOANZBNGDEJFH-UHFFFAOYSA-N 2,5-dihydro-1h-triazole Chemical compound C1NNN=C1 SYOANZBNGDEJFH-UHFFFAOYSA-N 0.000 description 1
- JKFYKCYQEWQPTM-UHFFFAOYSA-N 2-azaniumyl-2-(4-fluorophenyl)acetate Chemical compound OC(=O)C(N)C1=CC=C(F)C=C1 JKFYKCYQEWQPTM-UHFFFAOYSA-N 0.000 description 1
- ZVNPWFOVUDMGRP-UHFFFAOYSA-N 4-methylaminophenol sulfate Chemical compound OS(O)(=O)=O.CNC1=CC=C(O)C=C1.CNC1=CC=C(O)C=C1 ZVNPWFOVUDMGRP-UHFFFAOYSA-N 0.000 description 1
- IRLIJBLFDXFMPT-UHFFFAOYSA-N 6-ethoxy-2-[2-(4-nitrophenyl)ethenyl]quinoline Chemical compound C(C)OC=1C=C2C=CC(=NC2=CC1)C=CC1=CC=C(C=C1)[N+](=O)[O-] IRLIJBLFDXFMPT-UHFFFAOYSA-N 0.000 description 1
- 101100422770 Caenorhabditis elegans sup-1 gene Proteins 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 235000005979 Citrus limon Nutrition 0.000 description 1
- 244000131522 Citrus pyriformis Species 0.000 description 1
- 229910021612 Silver iodide Inorganic materials 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000002508 contact lithography Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000031700 light absorption Effects 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 229940045105 silver iodide Drugs 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- ZRRGOUHITGRLBA-UHFFFAOYSA-N stattic Chemical compound [O-][N+](=O)C1=CC=C2C=CS(=O)(=O)C2=C1 ZRRGOUHITGRLBA-UHFFFAOYSA-N 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
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
- G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
- G03C1/485—Direct positive emulsions
- G03C1/48592—Positive image obtained by various effects other than photohole bleaching or internal image desensitisation, e.g. Sabatier, Clayden effect
-
- 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
- G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
- G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
- G03C1/36—Desensitisers
Definitions
- This invention relates to photographic emulsions, and particularly to a direct positive photographic emulsion containing desensitizing dyes or compounds.
- a further object is to provide a direct positive emulsion in which high contrast images can be obtained.
- a still further object is to provide a method of producing direct positive images of low minimum density.
- the photographic emulsion used in our process is a silver chloride emulsion containing substantially no silver bromide or silver iodide.
- the desensitizing compound in amounts ranging from 0.1 gram to 2 grams ofcompound per 100 grams of silver chloride.
- the emulsion is then coated on a support and flashed with white light to fog it. It is then exposed to an image through a yellow filter-and developed in the usual way to produce a positive image.
- the reversal speed of the emulsion is approximately /400 that of ordinary contact printing paper.
- the desensitizing compounds used according to our invention are benzothiazole, quinoline, indolenine, benzotriazole, and rhodanine compounds having one or more nitro groups attached to a benzene nucleus which is either a part of the 1 heterocyclic compound or is attached to it through a doubly-bonded carbon to carbon chain.
- the emulsion is coated on the sup- 1 port, which may be of paper, glass, synthetic resin, or other suitable material.
- the emulsion is then flashed to a high density with white light.
- the fiash exposure should be of sufficient intensity to produce a high density upon development, although not necessarily the maximum density which the emulsion is capable of producing.
- a very heavy flash exposure requires a longer exposure to yellow light to remove its effect.
- the emulsion may also be fogged chemically rather than by light, and in this case the fogging may be done before or after addition of the reversing compound using non-sulfide fogging reagents.
- Addition of formaldehyde to the emulsion is a suitable way of fogging the emulsion chemically. In this case no flash exposure is needed, and the only exposure-necessary to give a positive image directly is the image-forming exposure. through the-yellow filter.
- the reversal exposure is made with minus blue light, that is, light 'of 500 to 700 m wavelength.
- a No. 12 or No. 15 filter (Wratten Light Filters, Eastman Kodak Co., 1945) may be used over the light source to produce reversing'light, or even a No. 2A filter if the blue speed of the emulsion is sufficiently, low. Maximum reversal is obtained at 520 to 540 m wavelength.
- Eacample 1 This example illustrates fogging by light after addition. of; the reversing compound.
- the prefiashed material can be exposed to an image with light modulated by a Wratten No. 15 filter.
- Example 2 This example illustrates chemical fogging before addition of the reversing compound.
- the emulsions made according to our invention produce a low minimum density and a high maximum density on reversal. They :are -es-- pecially useful for reproduction of document letters and drawings.
- a direct positive photographic emulsion comprising a strongly fogged silver chloride emulsion containing a compound selected from the class consisting of benzothiazole, quinoline, indolenine;
- a direct positive photographic emulsion comprising a strongly fogged silver chloride emulsion containing Z-(p-nitrostyryl) quinoline metho-ptoluene sulfon'ate.
- a direct positive photographic emulsion comprising a strongly fogged silver chloride emulsioncontaining a 6-nitro-1 2,3-benzotriazole.
- the method of making a direct positive photographic emulsion which comprises precipitate ing silver chloride in gelatin, adding to the emul-' sion a compound selected from the class consist-" ing of benzothiazole, quinoline, indolenine, ben-j zotriazole and rhodanine compounds and their alkyl quaternary salts having at least one nitro group attachedto a benzene nucleus and strongly fogging the emulsion in the presence of said compound.
- a direct positive photographic emulsion which comprises precipitating silver chloride in gelatin, chemically strongly fogging the emulsion and then adding to it a compound selected from the class consisting of benzothiazole, quinoline, indolenine, benzotriazole and rhodanine compounds and their alkyl quaternary salts having at least one nitro group attached to a benzene nucleus.
- photographic emulsion which comprises precipiphotographic emulsion which comprises precipitating silver chloride in gelatin, adjusting the emulsion to an alkaline condition, strongly fogging said emulsion chemically with formaldehyde, adjusting the emulsion to an acid condition and mixing with it a 2-nitrostyryl benzothiazole quaternary salt.
Landscapes
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- General Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BE489729D BE489729A (en(2012)) | 1948-06-29 | ||
US35987A US2541472A (en) | 1948-06-29 | 1948-06-29 | Direct positive emulsion containing desensitizing dye |
FR989400D FR989400A (fr) | 1948-06-29 | 1949-06-21 | Nouvelles émulsions photographiques et procédé pour leur préparation |
GB17049/49A GB667206A (en) | 1948-06-29 | 1949-06-28 | Improvements in photographic processes and materials therefor |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US35987A US2541472A (en) | 1948-06-29 | 1948-06-29 | Direct positive emulsion containing desensitizing dye |
Publications (1)
Publication Number | Publication Date |
---|---|
US2541472A true US2541472A (en) | 1951-02-13 |
Family
ID=21885938
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US35987A Expired - Lifetime US2541472A (en) | 1948-06-29 | 1948-06-29 | Direct positive emulsion containing desensitizing dye |
Country Status (4)
Country | Link |
---|---|
US (1) | US2541472A (en(2012)) |
BE (1) | BE489729A (en(2012)) |
FR (1) | FR989400A (en(2012)) |
GB (1) | GB667206A (en(2012)) |
Cited By (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2614927A (en) * | 1949-06-01 | 1952-10-21 | Eastman Kodak Co | Rapid processing of photographic materials |
US2774668A (en) * | 1953-05-28 | 1956-12-18 | Polaroid Corp | Process and product for forming color images from complete dyes |
US2947629A (en) * | 1958-09-17 | 1960-08-02 | Eastman Kodak Co | Nitrosopyrimidine desensitizing compounds and photographic emulsions containing them |
US2954292A (en) * | 1957-10-04 | 1960-09-27 | Ilford Ltd | Photographic desensitising compounds |
US2965485A (en) * | 1957-08-19 | 1960-12-20 | Ilford Ltd | Photographic desensitising compounds |
US3023102A (en) * | 1957-09-24 | 1962-02-27 | Gen Aniline & Film Corp | Direct positive photographic emulsion |
US3062651A (en) * | 1959-01-21 | 1962-11-06 | Eastman Kodak Co | Unhardened, fogged emulsions and method of processing to positive images |
US3189456A (en) * | 1961-06-19 | 1965-06-15 | Du Pont | Radiation-sensitive emulsions and elements and their preparation |
DE977335C (de) * | 1953-03-16 | 1965-12-16 | Agfa Ag | Verfahren zur Verminderung der Blauempfindlichkeit von photographischen Halogensilberemulsionen |
US3237008A (en) * | 1961-01-19 | 1966-02-22 | Eastman Kodak Co | Roomlight handling radiographic element including an x-ray sensitive layer overcoated with a dye desensitized silver halide emulsion |
US3250618A (en) * | 1959-05-13 | 1966-05-10 | Eastman Kodak Co | Thermal resensitization of desensitized silver halide photographic emulsions |
US3278307A (en) * | 1961-11-21 | 1966-10-11 | Eastman Kodak Co | Photographic process for producing prints stabilized against print-out |
US3284203A (en) * | 1961-05-02 | 1966-11-08 | Fuji Photo Film Co Ltd | Direct positive photographic materials |
US3295969A (en) * | 1961-04-12 | 1967-01-03 | Eastman Kodak Co | Photographic spirit duplicating process |
US3364026A (en) * | 1963-02-14 | 1968-01-16 | Eastman Kodak Co | Fogged silver halide direct positive solarizing elements containing merocyanine dyes |
US3367779A (en) * | 1965-01-21 | 1968-02-06 | Fuji Photo Film Co Ltd | Direct positive silver halide photographic materials |
US3372031A (en) * | 1963-08-28 | 1968-03-05 | Ilford Ltd | Direct positive silver halide element with contiguous colloid layer containing developing agent |
US3713832A (en) * | 1968-07-15 | 1973-01-30 | Fuji Photo Film Co Ltd | Solarization type silver halide emulsion containing a halogenated hydroxyphthalein sensitizing dye and a desensitizing compound |
US3988154A (en) * | 1974-02-19 | 1976-10-26 | Eastman Kodak Company | Photographic supports and elements utilizing photobleachable omicron-nitroarylidene dyes |
US3988156A (en) * | 1974-02-19 | 1976-10-26 | Eastman Kodak Company | Photographic supports and elements utilizing photobleachable o-nitroarylidene dyes |
US4271263A (en) * | 1980-05-15 | 1981-06-02 | Minnesota Mining And Manufacturing Company | Thermally developable photosensitive compositions containing acutance agents |
US4308379A (en) * | 1980-05-15 | 1981-12-29 | Minnesota Mining And Manufacturing Company | Acutance agents for use in thermally developable photosensitive compositions |
US4404277A (en) * | 1981-08-21 | 1983-09-13 | Minnesota Mining And Manufacturing Company | Desensitizing dyes for photographic emulsions |
EP0754967A1 (en) | 1995-07-14 | 1997-01-22 | Agfa-Gevaert N.V. | Photographic direct positive material containing a particular stabilizer |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2865749A (en) * | 1956-11-06 | 1958-12-23 | Eastman Kodak Co | Stabilized photographic emulsions |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2066099A (en) * | 1928-01-31 | 1936-12-29 | Agfa Ansco Corp | Photographic emulsion |
US2271229A (en) * | 1939-11-10 | 1942-01-27 | Eastman Kodak Co | Fog inhibitor for photographic developers |
US2324123A (en) * | 1941-07-08 | 1943-07-13 | Eastman Kodak Co | Fog inhibitor for photographic developers |
US2384593A (en) * | 1943-08-06 | 1945-09-11 | Eastman Kodak Co | Antifoggant |
-
0
- BE BE489729D patent/BE489729A/xx unknown
-
1948
- 1948-06-29 US US35987A patent/US2541472A/en not_active Expired - Lifetime
-
1949
- 1949-06-21 FR FR989400D patent/FR989400A/fr not_active Expired
- 1949-06-28 GB GB17049/49A patent/GB667206A/en not_active Expired
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2066099A (en) * | 1928-01-31 | 1936-12-29 | Agfa Ansco Corp | Photographic emulsion |
US2271229A (en) * | 1939-11-10 | 1942-01-27 | Eastman Kodak Co | Fog inhibitor for photographic developers |
US2324123A (en) * | 1941-07-08 | 1943-07-13 | Eastman Kodak Co | Fog inhibitor for photographic developers |
US2384593A (en) * | 1943-08-06 | 1945-09-11 | Eastman Kodak Co | Antifoggant |
Cited By (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2614927A (en) * | 1949-06-01 | 1952-10-21 | Eastman Kodak Co | Rapid processing of photographic materials |
DE977335C (de) * | 1953-03-16 | 1965-12-16 | Agfa Ag | Verfahren zur Verminderung der Blauempfindlichkeit von photographischen Halogensilberemulsionen |
US2774668A (en) * | 1953-05-28 | 1956-12-18 | Polaroid Corp | Process and product for forming color images from complete dyes |
US2965485A (en) * | 1957-08-19 | 1960-12-20 | Ilford Ltd | Photographic desensitising compounds |
US3023102A (en) * | 1957-09-24 | 1962-02-27 | Gen Aniline & Film Corp | Direct positive photographic emulsion |
US2954292A (en) * | 1957-10-04 | 1960-09-27 | Ilford Ltd | Photographic desensitising compounds |
US2947629A (en) * | 1958-09-17 | 1960-08-02 | Eastman Kodak Co | Nitrosopyrimidine desensitizing compounds and photographic emulsions containing them |
US3062651A (en) * | 1959-01-21 | 1962-11-06 | Eastman Kodak Co | Unhardened, fogged emulsions and method of processing to positive images |
US3250618A (en) * | 1959-05-13 | 1966-05-10 | Eastman Kodak Co | Thermal resensitization of desensitized silver halide photographic emulsions |
US3237008A (en) * | 1961-01-19 | 1966-02-22 | Eastman Kodak Co | Roomlight handling radiographic element including an x-ray sensitive layer overcoated with a dye desensitized silver halide emulsion |
US3295969A (en) * | 1961-04-12 | 1967-01-03 | Eastman Kodak Co | Photographic spirit duplicating process |
US3284203A (en) * | 1961-05-02 | 1966-11-08 | Fuji Photo Film Co Ltd | Direct positive photographic materials |
US3189456A (en) * | 1961-06-19 | 1965-06-15 | Du Pont | Radiation-sensitive emulsions and elements and their preparation |
US3278307A (en) * | 1961-11-21 | 1966-10-11 | Eastman Kodak Co | Photographic process for producing prints stabilized against print-out |
US3364026A (en) * | 1963-02-14 | 1968-01-16 | Eastman Kodak Co | Fogged silver halide direct positive solarizing elements containing merocyanine dyes |
US3372031A (en) * | 1963-08-28 | 1968-03-05 | Ilford Ltd | Direct positive silver halide element with contiguous colloid layer containing developing agent |
US3367779A (en) * | 1965-01-21 | 1968-02-06 | Fuji Photo Film Co Ltd | Direct positive silver halide photographic materials |
US3713832A (en) * | 1968-07-15 | 1973-01-30 | Fuji Photo Film Co Ltd | Solarization type silver halide emulsion containing a halogenated hydroxyphthalein sensitizing dye and a desensitizing compound |
US3988154A (en) * | 1974-02-19 | 1976-10-26 | Eastman Kodak Company | Photographic supports and elements utilizing photobleachable omicron-nitroarylidene dyes |
US3988156A (en) * | 1974-02-19 | 1976-10-26 | Eastman Kodak Company | Photographic supports and elements utilizing photobleachable o-nitroarylidene dyes |
US4271263A (en) * | 1980-05-15 | 1981-06-02 | Minnesota Mining And Manufacturing Company | Thermally developable photosensitive compositions containing acutance agents |
US4308379A (en) * | 1980-05-15 | 1981-12-29 | Minnesota Mining And Manufacturing Company | Acutance agents for use in thermally developable photosensitive compositions |
US4404277A (en) * | 1981-08-21 | 1983-09-13 | Minnesota Mining And Manufacturing Company | Desensitizing dyes for photographic emulsions |
EP0754967A1 (en) | 1995-07-14 | 1997-01-22 | Agfa-Gevaert N.V. | Photographic direct positive material containing a particular stabilizer |
Also Published As
Publication number | Publication date |
---|---|
BE489729A (en(2012)) | |
FR989400A (fr) | 1951-09-07 |
GB667206A (en) | 1952-02-27 |
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