US2378203A - Ethyl trichloroacetate antifoggant - Google Patents
Ethyl trichloroacetate antifoggant Download PDFInfo
- Publication number
- US2378203A US2378203A US518121A US51812144A US2378203A US 2378203 A US2378203 A US 2378203A US 518121 A US518121 A US 518121A US 51812144 A US51812144 A US 51812144A US 2378203 A US2378203 A US 2378203A
- Authority
- US
- United States
- Prior art keywords
- emulsion
- fog
- antifoggant
- ethyl trichloroacetate
- tests
- 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
- SJMLNDPIJZBEKY-UHFFFAOYSA-N ethyl 2,2,2-trichloroacetate Chemical compound CCOC(=O)C(Cl)(Cl)Cl SJMLNDPIJZBEKY-UHFFFAOYSA-N 0.000 title description 8
- 239000000839 emulsion Substances 0.000 description 43
- 230000002401 inhibitory effect Effects 0.000 description 8
- 238000012360 testing method Methods 0.000 description 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 229910052709 silver Inorganic materials 0.000 description 6
- 239000004332 silver Substances 0.000 description 6
- 108010010803 Gelatin Proteins 0.000 description 5
- 229920000159 gelatin Polymers 0.000 description 5
- 239000008273 gelatin Substances 0.000 description 5
- 235000019322 gelatine Nutrition 0.000 description 5
- 235000011852 gelatine desserts Nutrition 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- 230000035945 sensitivity Effects 0.000 description 3
- -1 silver halide Chemical class 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 230000029087 digestion Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- CYXJEHCKVOQFOV-UHFFFAOYSA-N (4-amino-2-methylphenyl) hydrogen sulfate Chemical compound CC1=CC(N)=CC=C1OS(O)(=O)=O CYXJEHCKVOQFOV-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- QUPDWYMUPZLYJZ-UHFFFAOYSA-N ethyl Chemical class C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000013101 initial test Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 150000003378 silver Chemical class 0.000 description 1
- ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 238000005303 weighing Methods 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
- G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
- G03C1/34—Fog-inhibitors; Stabilisers; Agents inhibiting latent image regression
Definitions
- This invention relates to fog inhibitors for photographic emulsions and to photographic emulsions containing them.
- Photographic fog is of two types, local and general. Local fog is formed by exposure of the film or plate at undesired points, as by a light leak in the camera, or by local action of chemicals. General fog or, as it is sometimes known, chemical fog, is formed in a' number of ways. It may be caused by the conditions under which the film orplate is stored, such as conditions of high temperature or unusually long time of storage.
- the nature of the emulsion may also produce chemical fog, as well as the conditions of development of the emulsion, as by development for protracted periods of time or at tem-. peratures above normal. Highly sensitive emulsions are more likely to fog than those of lower sensitivity. I am concerned primarily with general or chemical fog.
- a further object is to provide a novel antifoggant which does not markedly lower the sensitivity of the emulsion.
- the required digestion temperature that is, about 60 C. and as soon as this temperature was reached a certain amount of the compound to be tested, e. g., grams of ethyl trichloroacetate, dissolved in 300 cc. of methyl alcohol, was added. Digestion was then continued for minutes at the specified temperature and the emulsion was then chilled and stored in preparation for shredding and washing. One of these portions received no additions other than the required gelatin and it served as the control for all the portions originating from the same precipitation of silver halide.
- each emulsion was heated to the optimum point for maximum speed and gamma with acceptable fog. Unsensitized and panchromatized samples of each emulsion so finished were coated by machine on glass plates. After the plates were dry, a series of sensitometric tests were made on them. The data were then compared with those of the check emulsion containing 'no addendum. These tests include initial tests for speed, gamma and fog, made on the day after coating, similar tests on a second set of plates incubated at 120 F., dry heat, for 6 days and a third set of tests made on a third set of plates after having been kept under tropical conditions for 14 days. The ftropical conditions are simulated by varying the temperature and humidity through a cycle to reproduce day and night conditions in tropical climates. Plates for each of these tests were developed for 3 minutes at 65 C. in Kodak D-19 developer which had the following composition:
- the amount of fog was determined by reading the density at the toe of the curve after exposure and development of the emulsion, in the usual Each portion was then heated to manner.
- the amount of the fog inhibiting agent used in the emulsion will depend upon the composition or the agent and upon the type of emulsion. In general, the amount of fog inhibiting agent used will vary from 1 gram to 15 grams per 1000 cc. of wet emulsion. It will be understood that more or less than this amount may be used. Generally, however, if a greater amount is used in the emulsion, either no increased fog inhibiting effect is obtained or there is a decrease in the
- the antifoggant may be incorporated by mixing it with any suitable solvent which is inert with respect to the emulsion such as' water, methyl alcohol, ethyl alcohol, acetone and others.
- the fog inhibiting agent which I have described may be used in various kinds of photographic emulsions. In addition to being useiul in ordinary non-sensitized emulsions, it may be used in orthochromatic, panchromatic and X-ray emulsions. Various silver salts may be used as the sensitive salt such as silver chlorobromide.
- the dispersing agent may be gelatin or other suitable colloid such as collodion, albumen, cellulose organic derivatives or synthetic resins.
- my fog inhibiting agent may also be incorporated in an overcoating or intermediate layer in the photographic element containing the sensitive emulsion layer.
- a gelatino-silver halide emulsion containing a fog inhibiting amount of ethyl trichloroacetate 1.
- the method of reducing the amount of fog produced upon development of a silver halide emulsion which comprises developing said emulsion in the presence of a fog-inhibiting amount of ethyl trichloroacetate.
Landscapes
- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- General Physics & Mathematics (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
Description
tendency to form a deposit of silver in the emul- Patented June 12, 1945 ETHYL TBICHIDROACETATE ANTIFOGGAN '1 George E. Fallesen, Rochester, N. Y., assignor to Eastman Kodak Company, Rochester, N. Y., a
corporation of New Jersey -3 Claims.
This invention relates to fog inhibitors for photographic emulsions and to photographic emulsions containing them.
It is known that photographic emulsions, particularly ultra-sensitive emulsions, exhibit a 5 sion. This deposit extends more or less uniformly over the entire emulsion and is known as fog. Photographic fog is of two types, local and general. Local fog is formed by exposure of the film or plate at undesired points, as by a light leak in the camera, or by local action of chemicals. General fog or, as it is sometimes known, chemical fog, is formed in a' number of ways. It may be caused by the conditions under which the film orplate is stored, such as conditions of high temperature or unusually long time of storage. The nature of the emulsion may also produce chemical fog, as well as the conditions of development of the emulsion, as by development for protracted periods of time or at tem-. peratures above normal. Highly sensitive emulsions are more likely to fog than those of lower sensitivity. I am concerned primarily with general or chemical fog.
It is an object of the present invention to provide a fog inhibiting agent for ultra-sensitive photographic emulsions and thereby to preserve the emulsions against deterioration causing fog. A further object is to provide a novel antifoggant which does not markedly lower the sensitivity of the emulsion.
These objects are accomplished by developing an exposed silver halide emulsion in the presence of ethyl trichloroacetate, preferably by incorporating it in the emulsion.
the required digestion temperature, that is, about 60 C. and as soon as this temperature was reached a certain amount of the compound to be tested, e. g., grams of ethyl trichloroacetate, dissolved in 300 cc. of methyl alcohol, was added. Digestion was then continued for minutes at the specified temperature and the emulsion was then chilled and stored in preparation for shredding and washing. One of these portions received no additions other than the required gelatin and it served as the control for all the portions originating from the same precipitation of silver halide.
After washing, each emulsion was heated to the optimum point for maximum speed and gamma with acceptable fog. Unsensitized and panchromatized samples of each emulsion so finished were coated by machine on glass plates. After the plates were dry, a series of sensitometric tests were made on them. The data were then compared with those of the check emulsion containing 'no addendum. These tests include initial tests for speed, gamma and fog, made on the day after coating, similar tests on a second set of plates incubated at 120 F., dry heat, for 6 days and a third set of tests made on a third set of plates after having been kept under tropical conditions for 14 days. The ftropical conditions are simulated by varying the temperature and humidity through a cycle to reproduce day and night conditions in tropical climates. Plates for each of these tests were developed for 3 minutes at 65 C. in Kodak D-19 developer which had the following composition:
Monomethyl-p-aminophenol sulfate,
2,378,203 UNITED STATES PATENT OFFICE Ethyl trichloroacetate, 013000002115, may be grams" incorporated in an emulsion which is intended gggm iggz (deslccated) "33"" g 8 to be used directly after emulsification or one Sodium j gjg ggia which is subjected to ripening. Potassium bromide 5 The antifoggant properties of ethyl trichloro- Water to 65 1 acetate were tested as follows:
Silver iodobromide was precipitated in 0.8% gelatin solution. After precipitation was complete, this entire volume of emulsion was cooled The results of these tests are tabulated below, in each case the ethyl trichloroacetate being added to an unsensitized emulsion:
' Tropical condition 14 6 d5 y 120 F. incuba- Initial tog tests 21:58 incubation log on 08 tests Amount Emulsion Emulsion Emulsion Emulsion Emulsion Emulsion with comwithout with oomwithout with comwithout pound compound pound compound pound compound and divided into portions weighing 1643 grams each. To each portion was added enough gelatin to increase the gelatin concentration to approximately 6.6%.
' The amount of fog was determined by reading the density at the toe of the curve after exposure and development of the emulsion, in the usual Each portion was then heated to manner.
' sensitivity of the emulsion.
The amount of the fog inhibiting agent used in the emulsion will depend upon the composition or the agent and upon the type of emulsion. In general, the amount of fog inhibiting agent used will vary from 1 gram to 15 grams per 1000 cc. of wet emulsion. It will be understood that more or less than this amount may be used. Generally, however, if a greater amount is used in the emulsion, either no increased fog inhibiting effect is obtained or there is a decrease in the The antifoggant may be incorporated by mixing it with any suitable solvent which is inert with respect to the emulsion such as' water, methyl alcohol, ethyl alcohol, acetone and others.
The fog inhibiting agent which I have described may be used in various kinds of photographic emulsions. In addition to being useiul in ordinary non-sensitized emulsions, it may be used in orthochromatic, panchromatic and X-ray emulsions. Various silver salts may be used as the sensitive salt such as silver chlorobromide. The dispersing agent may be gelatin or other suitable colloid such as collodion, albumen, cellulose organic derivatives or synthetic resins.
In addition to its use in the sensitive emulsion itself, my fog inhibiting agent may also be incorporated in an overcoating or intermediate layer in the photographic element containing the sensitive emulsion layer.
It is to be understood that I contemplate as included within my invention all modifications and equivalents falling within the scope of the appended claims.
I claim:
1. A gelatino-silver halide emulsion containing a fog inhibiting amount of ethyl trichloroacetate.
2. A gelatino-silver halide emulsion containing from 1 to 15 grams per liter of wet emulsion of ethyl trichloroacetate.
3. The method of reducing the amount of fog produced upon development of a silver halide emulsion which comprises developing said emulsion in the presence of a fog-inhibiting amount of ethyl trichloroacetate.
GEORGE E. FALLESEN.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US518121A US2378203A (en) | 1944-01-13 | 1944-01-13 | Ethyl trichloroacetate antifoggant |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US518121A US2378203A (en) | 1944-01-13 | 1944-01-13 | Ethyl trichloroacetate antifoggant |
Publications (1)
Publication Number | Publication Date |
---|---|
US2378203A true US2378203A (en) | 1945-06-12 |
Family
ID=24062641
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US518121A Expired - Lifetime US2378203A (en) | 1944-01-13 | 1944-01-13 | Ethyl trichloroacetate antifoggant |
Country Status (1)
Country | Link |
---|---|
US (1) | US2378203A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2635048A (en) * | 1948-07-06 | 1953-04-14 | Polaroid Corp | Photographic transfer product and process |
US2657138A (en) * | 1950-01-03 | 1953-10-27 | Leonard A Robbins | Photographic film developing composition containing beta, beta'-di-chloroethyl ether |
US2732303A (en) * | 1953-09-16 | 1956-01-24 | Antifoggevg and hardening agents for | |
US4468454A (en) * | 1983-06-10 | 1984-08-28 | E. I. Du Pont De Nemours And Company | Antifoggant process |
-
1944
- 1944-01-13 US US518121A patent/US2378203A/en not_active Expired - Lifetime
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2635048A (en) * | 1948-07-06 | 1953-04-14 | Polaroid Corp | Photographic transfer product and process |
US2657138A (en) * | 1950-01-03 | 1953-10-27 | Leonard A Robbins | Photographic film developing composition containing beta, beta'-di-chloroethyl ether |
US2732303A (en) * | 1953-09-16 | 1956-01-24 | Antifoggevg and hardening agents for | |
US4468454A (en) * | 1983-06-10 | 1984-08-28 | E. I. Du Pont De Nemours And Company | Antifoggant process |
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