US2454001A - Control of contrast with aromatic diamine color developers - Google Patents
Control of contrast with aromatic diamine color developers Download PDFInfo
- Publication number
- US2454001A US2454001A US627329A US62732945A US2454001A US 2454001 A US2454001 A US 2454001A US 627329 A US627329 A US 627329A US 62732945 A US62732945 A US 62732945A US 2454001 A US2454001 A US 2454001A
- Authority
- US
- United States
- Prior art keywords
- color
- film
- contrast
- aromatic diamine
- layer
- 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
- 150000004984 aromatic diamines Chemical class 0.000 title description 10
- 239000000047 product Substances 0.000 description 15
- 239000000975 dye Substances 0.000 description 13
- 108090000623 proteins and genes Proteins 0.000 description 13
- 102000004169 proteins and genes Human genes 0.000 description 13
- 239000003795 chemical substances by application Substances 0.000 description 12
- 238000000354 decomposition reaction Methods 0.000 description 12
- 239000000839 emulsion Substances 0.000 description 10
- 238000000034 method Methods 0.000 description 7
- 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 5
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 5
- 229910052708 sodium Inorganic materials 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 229910052709 silver Inorganic materials 0.000 description 4
- 239000004332 silver Substances 0.000 description 4
- 239000001888 Peptone Substances 0.000 description 3
- 108010080698 Peptones Proteins 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 235000019319 peptone Nutrition 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 150000004985 diamines Chemical class 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
- XTBFKMDOQMQYPP-UHFFFAOYSA-N 4-n,4-n-diethylbenzene-1,4-diamine;hydron;chloride Chemical compound Cl.CCN(CC)C1=CC=C(N)C=C1 XTBFKMDOQMQYPP-UHFFFAOYSA-N 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical group OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 1
- 229910001864 baryta Inorganic materials 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 239000007857 degradation product Substances 0.000 description 1
- MQRJBSHKWOFOGF-UHFFFAOYSA-L disodium;carbonate;hydrate Chemical compound O.[Na+].[Na+].[O-]C([O-])=O MQRJBSHKWOFOGF-UHFFFAOYSA-L 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000001013 indophenol dye Substances 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001184 polypeptide Polymers 0.000 description 1
- 150000003142 primary aromatic amines Chemical class 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 230000007065 protein hydrolysis Effects 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000001043 yellow dye Substances 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
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/407—Development processes or agents therefor
- G03C7/413—Developers
Definitions
- This invention relates to color photography, and more particularly to a development of color images by means of aromatic diamine developing agents in the presence of protein decomposition products in order to control the contrast of color images obtained upon coupler development.
- the green-sensitive emulsion layer containing a color-former for the magenta dye image.
- the bottom layer is a redsensitive emulsion layer containing a color-former for the cyan dye image.
- the color-negative film is made up in the same manner as the colorreversible film, with the exception that it may contain a layer of clear gelatin between the redsensitive layer and the green-sensitive layer.
- the color-reversible opaque materia1 is prepared in the same manner as the color-reversible film, with the exception that the base consists of an opaque white film.
- the color paper is made up in the same manner as the color-reversible film, with the exception that the emulsions are coated on a baryta-coated paper base.
- suitable aromatic diamine developing agents which may be employed with the protein decomposition products
- p-phen'ylenediamine p-aminoethylanor primary amino group in the phenyl nucleus which enables the oxidation product of the developer to couple with the color-former to form a dye image in the emulsion adjacent to the individual particles of the silver image.
- the silver image may be removed by bleaching in the well-known manner to leave the color image in the emulsion-
- a suitable developing solution is prepared as follows:
- p-Diethylamino aniline hydrochloride "grams" 2.5 Sodium sulfite (anhydrous) do 1.0 Sodium carbonate (monohydrate) do 67.5 Potassium bromide do 2.0 Water to make liter 1
- concentration of protein decomposition products such as sodium lysalbinate, peptone, gelatose and similarprotein degradation products may range from to grams per liter of developer solution. A concentration approaching grams per liter has the tendency of not only reducing the contrast of the cyan image, but may lead to stain and reduction of the maximum density of the dye image. The optimum concentration resulting in optimal color balance can be readily ascertained for the various types of color film and papers and for the various species of diamine developing agents by a few routine experiments.
- Example I minutes in a color developer as above described.
- Th n t ur a an? 9 a ll strated in Figure 1 were obtained by reading the color densities in the individual yellow, magenta and cyan layers, by employing the proper filters in a photoelectric densitometer in a known manner. From this figure, it will be observed that the cyan layer, C, has too steep a gradation to obtain a good color balance.
- Example II A multi-color subtractive negative film was developed with a color developer as hereinbefore described without the presence of a protein decomposition product.
- the density curves obtained were plotted as A, B, and C shown in Figure 2,. From these curves, it will be observed that their shape is quite irregular and substantially altered,
- Example III Similar results as obtained in Examples I and II were procured when peptone and gelatose were substituted for sodium lysalbinate in equal amounts.
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Description
Nov. 16, 1948. F. w. H. MUELLER 2,454,001
7 CONTROL OF CONTRAST WITH AROMATIC DIAMINE COLOR DEVELOPERS Filed NOV. 8, 1945 COL-0R POSFHVE FlLM R 7. t V} Z m D LOG ExPosuRE' 3.0 COLOR NEGATIVE. Fn..M
t m 2 L5 m G Fm. Z
LOG EXPOSURE M INVENTOR FRITZ W.H. MUELLER 8Y3 Q M ATToR NEY Patented Nov. 16, 1948 CONTROL OF CONTRAST WITH ,AROMATIC DIAMIN E COLOR DEVELOPERS Fritz W. H. Mueller, Binghamton,
N. Y., assignor to General Aniline & Film Corporation, New York, N. Y., a corporation of Delaware Application November 8, 1945, Serial No. 627,329
4 Claims.
This invention relates to color photography, and more particularly to a development of color images by means of aromatic diamine developing agents in the presence of protein decomposition products in order to control the contrast of color images obtained upon coupler development.
In color photography, it is well-known that dye images are formed by a coupling reaction of an oxidized primary aromatic amine developing agent with a suitable organic compound having an active methylene or reactive ethenol group. As development proceeds, the corresponding azomethine or indophenol dyes are formed in situ with the silver image. Speed and gradation control are readily accomplished in the usual dye coupling process, but difficulties are encountered in controlling the contrast or gamma of the color image to obtain the proper color balance. Color developers which are-used in subtractive color processes are Well-known in the prior art, and comprise reducing agents which, when acting upon exposed silver-halide, produce oxidation products which in turn yield insoluble dye images with suitable color couplers. Such color couplers may be either incorporated as non-difiusing color components in the individual layers of a, multicolor subtractive process or may be added to the color developer in difiusible form.
It is known that natural proteins of very high molecular weight and protein decomposition products of medium to high molecular weight within the range of the molecular weights of lysalbinic acid, gelatose and the like, have been added to ordinary black and white developers, 1. e., developers containing mono-amines alone, or in combination With hydroquinone or other adjuvants in order to yield softer silver images of finer grain. Developing agents of the monoamine type, whether alone or in combination with other adjuvants and in the presence of protein decomposition products as described in United States Patent 2,164,687, do not control the contrast or gamma of the color images produced in multi-color subtractive processes. In other words, fine grain developers do not exert a selective influence on the gamma of the characteristic curve representing the dependence of developed color density upon the logarithm of exposure in the individual layer of the multi-layer subtractive color film.
I have discovered that the addition of a relatively small quantity of a protein decomposition product of medium to high molecular weight, as described in U. S. 2,164,687 to color developers of the aromatic diamine type gives an improvement in color balance 'of the dye image by selective adjustment of the gradation of the characteristic curves of the magenta and even more of the cyan layer. This discovery is of special value in subtractive multi-layer film where the various layers are developed simultaneously by a, single color developer solution. It appears that the rate of penetration of the color developer, and the rate of coupling of the color coupler varies, and that the color balance is not distorted if the gamma of the characteristic curves in the three individual layers is approximately the same. In other words, if one of the layers shows an excessive contrast, the color balance is inferior and color falsification results in the final picture.
The photographic multi-layer materials, which may be processed with the developers of the present invention, are color-reversible film, colornegative film, color-positive film, color-reversible printing material coated on a white opaque film base or color-positive printing material coated on paper. A color-reversible film, as prepared according to United States Patent 2,186,849, consists of an integral tripack emulsion coated on the usual clear cellulose acetate or nitrate film base. Each of the three emulsion layers contains a color-former and is sensitized to one of the primary colors of light. The top layer is blue-sensitive and contains a color-former for the yellow dye image. A filter layer, yellow in color and blue absorbing, lies underneath the top layer. Below this filter layer lies the green-sensitive emulsion layer containing a color-former for the magenta dye image. The bottom layer is a redsensitive emulsion layer containing a color-former for the cyan dye image. The color-negative film is made up in the same manner as the colorreversible film, with the exception that it may contain a layer of clear gelatin between the redsensitive layer and the green-sensitive layer. The color-reversible opaque materia1 is prepared in the same manner as the color-reversible film, with the exception that the base consists of an opaque white film. The color paper is made up in the same manner as the color-reversible film, with the exception that the emulsions are coated on a baryta-coated paper base. When the silver-halide latent image is developed with a primary aromatic amino developer, the oxidation product of the developing agent reacts-with the color-formers to give a colored dye image.
As examples of suitable aromatic diamine developing agents which may be employed with the protein decomposition products, there may be mentioned p-phen'ylenediamine, p-aminoethylanor primary amino group in the phenyl nucleus which enables the oxidation product of the developer to couple with the color-former to form a dye image in the emulsion adjacent to the individual particles of the silver image. The silver image may be removed by bleaching in the well-known manner to leave the color image in the emulsion- A suitable developing solution is prepared as follows:
p-Diethylamino aniline hydrochloride "grams" 2.5 Sodium sulfite (anhydrous) do 1.0 Sodium carbonate (monohydrate) do 67.5 Potassium bromide do 2.0 Water to make liter 1 The concentration of protein decomposition products such as sodium lysalbinate, peptone, gelatose and similarprotein degradation products may range from to grams per liter of developer solution. A concentration approaching grams per liter has the tendency of not only reducing the contrast of the cyan image, but may lead to stain and reduction of the maximum density of the dye image. The optimum concentration resulting in optimal color balance can be readily ascertained for the various types of color film and papers and for the various species of diamine developing agents by a few routine experiments.
The present invention is illustrated by the ac companying drawing in which Figures 1 to 2represent typical characteristic curves of the color densities in the individual layers obtained on color positive and color negative films as described be,-
low by way of examples and the films treated in the manner set forth.
In Figures 1 to 2, wherein the ordinates represent densities and the abscissa represent the log of exposure, A, B, and C (which represent yellow, magenta and cyan, respectively) are the density curves for color positive and color negative films, respectively, which have been exposed and developed in an aromatic diamine developing agent in the ordinary manner, and A, B, and C, are the density curves for the same type of film exposed under the same conditions and 'treated with a diamine developing agent in the presence of a protein decomposition product in accordance with the present invention.
The following examples will serve to specifically describe the invention as applied to color positive and color negative films. These examples should not be construed as limiting or' restricting the present invention, but should be considered merely as illustrative.
Example I minutes in a color developer as above described.
Th n t ur a an? 9 a ll strated in Figure 1, were obtained by reading the color densities in the individual yellow, magenta and cyan layers, by employing the proper filters in a photoelectric densitometer in a known manner. From this figure, it will be observed that the cyan layer, C, has too steep a gradation to obtain a good color balance.
By adding 5 grams of sodium lysalbinate to a liter of the same color developer and developing a similarly exposed color positive film, the contrast of the cyan layer, C, was noticeably reduced as shown by the dotted line C, whereas the curves A (yellow) and B (magenta) were altered very slightly as shown by dotted lines A and B, respectively.
Example II A multi-color subtractive negative film was developed with a color developer as hereinbefore described without the presence of a protein decomposition product. The density curves obtained were plotted as A, B, and C shown in Figure 2,. From these curves, it will be observed that their shape is quite irregular and substantially altered,
By adding 5 grams of sodium lysalbinate to a liter of the same color developer and developing a similarly exposed color negative film, the shape of these curves, A, B, and C, are more uniform, particularly in the high densities, as shown by the dotted lines A, B, and C.
Example III Similar results as obtained in Examples I and II were procured when peptone and gelatose were substituted for sodium lysalbinate in equal amounts.
While I have herein disclosed the preferred embodiments of my invention, I do not desire to limit myself solely to the specific examples, since it will be readily apparent to those skilled in the art that precise ratios of protein decomposition products and the aromatic diamine developing agent may be varied and other materials having equivalent chemical or physical properties may be employed without departing from the spirit and scope thereof. As for example, instead of employing the protein decomposition products specifically disclosed herein, polypeptides either synthetically prepared or obtained by controlled protein hydrolysis in the known manner may be employed with satisfactory results. Accordingly, therefore, only such limitations should be imposed as are indicated in the appended claims.
I claim:
1. The process of preventing the formation of excessively contrasty dye images in the individual layers of a multi-layer color film containing silver-halide emulsions and color formers which comprises exposing the film and developing simultaneously all layers with a solution of an aromatic diamine developing agent containing a primary amino group and 5 to 15 grams per liter of said solution of a protein decomposi tion product of medium to high molecular weight substantially within the range of the molecular weights of lysalbinic acid and gelatose, the molecules of thesaid protein decomposition products being built up of at least five amino acids.
2. The process of preventing the formation of execssively contrasty dye images in the individual layers of a multi-layer color film containing silver-halide emulsions and color'formers which comprises exposing the film and developing simultaneously all layers with a solution of an. sweetie d st ld elqnin e t c lil e a primary amino group and 5 to 15 grams per liter of said solution of sodium lysalbinate.
3. The process of preventing the formation or excessively contrasty dye images in the individual layers of a multi-layer color film containing silver-halide emulsions and color formers which comprises exposing the film and developing simultaneously all layers with a solution of an aromatic diamine developing agent containing a primary amino gI'OllP and 5 to 15 grams per liter of said solution of gelatose.
4. The process of preventing the formation of excessively contrasty dye images in the individual layers of a multi-layer color film containing silver-halide emulsions and color formers which comprises exposing the film and developing simultaneously all layers with a solution of an aromatic diamine developing agent containing a primary amino group and 5 to 15 grams per liter of said solution of peptone.
FRITZ W. H. MUELLER.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS OTHER REFERENCES Henney, Handbook of Photography, Mc- Graw-Hill Book Company, Inc., 1939, pages 335 and 337 cited.
Riegel, Industrial Chemistry, Reinhold Publishing Corporation, 1937, page 620 cited.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US627329A US2454001A (en) | 1945-11-08 | 1945-11-08 | Control of contrast with aromatic diamine color developers |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US627329A US2454001A (en) | 1945-11-08 | 1945-11-08 | Control of contrast with aromatic diamine color developers |
Publications (1)
Publication Number | Publication Date |
---|---|
US2454001A true US2454001A (en) | 1948-11-16 |
Family
ID=24514223
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US627329A Expired - Lifetime US2454001A (en) | 1945-11-08 | 1945-11-08 | Control of contrast with aromatic diamine color developers |
Country Status (1)
Country | Link |
---|---|
US (1) | US2454001A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2699391A (en) * | 1950-01-11 | 1955-01-11 | Gen Aniline & Film Corp | Synthetic polypeptides of alpha-amino acids as restrainers in photographic emulsions |
US2710805A (en) * | 1952-10-09 | 1955-06-14 | Ilford Ltd | Production of silver halide photographic emulsions containing a synthetic polypeptide derivative |
DE962666C (en) * | 1953-03-13 | 1957-04-11 | Eastman Kodak Company, Rochester, N. Y. (V. St. A.) | Process for producing color photographic images by the color development process |
US2998314A (en) * | 1956-09-18 | 1961-08-29 | Agfa Ag | Color photography |
US4189319A (en) * | 1975-07-18 | 1980-02-19 | Gaf Corporation | Arginine or salt thereof as a development accelerator of color development of color photographic materials |
US4368255A (en) * | 1980-07-16 | 1983-01-11 | Ciba-Geigy Ag | Method of processing monochrome silver halide material |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB454622A (en) * | 1935-02-27 | 1936-09-29 | Eastman Kodak Co | Improvements in colour photography |
US2164687A (en) * | 1936-09-02 | 1939-07-04 | Firm Chem Fab Grunau Landshoff | Photographic developer and substances added in preparing the same |
US2200924A (en) * | 1938-06-24 | 1940-05-14 | Du Pont Film Mfg Corp | Bis-pyrazolonyl color former |
-
1945
- 1945-11-08 US US627329A patent/US2454001A/en not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB454622A (en) * | 1935-02-27 | 1936-09-29 | Eastman Kodak Co | Improvements in colour photography |
US2164687A (en) * | 1936-09-02 | 1939-07-04 | Firm Chem Fab Grunau Landshoff | Photographic developer and substances added in preparing the same |
US2200924A (en) * | 1938-06-24 | 1940-05-14 | Du Pont Film Mfg Corp | Bis-pyrazolonyl color former |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2699391A (en) * | 1950-01-11 | 1955-01-11 | Gen Aniline & Film Corp | Synthetic polypeptides of alpha-amino acids as restrainers in photographic emulsions |
US2710805A (en) * | 1952-10-09 | 1955-06-14 | Ilford Ltd | Production of silver halide photographic emulsions containing a synthetic polypeptide derivative |
DE962666C (en) * | 1953-03-13 | 1957-04-11 | Eastman Kodak Company, Rochester, N. Y. (V. St. A.) | Process for producing color photographic images by the color development process |
US2998314A (en) * | 1956-09-18 | 1961-08-29 | Agfa Ag | Color photography |
US4189319A (en) * | 1975-07-18 | 1980-02-19 | Gaf Corporation | Arginine or salt thereof as a development accelerator of color development of color photographic materials |
US4368255A (en) * | 1980-07-16 | 1983-01-11 | Ciba-Geigy Ag | Method of processing monochrome silver halide material |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2279406A (en) | Color process using cellulose ester emulsions | |
US3520690A (en) | Process for controlling dye gradation in color photographic element | |
US2350380A (en) | Photography | |
US3505068A (en) | Photographic element | |
US2927024A (en) | Multilayer color photographic film | |
US4902609A (en) | Photographic print material with increased exposure latitude | |
US2454001A (en) | Control of contrast with aromatic diamine color developers | |
US2258187A (en) | Integral mask for multicolor film | |
US2933391A (en) | Photographic emulsions containing 5-pyrazolone coupler compounds | |
US2592514A (en) | Multilayer photographic color film in which at least one layer contains a mixture of cyan, magenta, and yellow dye image intermediates | |
US3547640A (en) | Multicolor photographic elements | |
US4306015A (en) | Color photographic material | |
US3246987A (en) | Method for elimination of reversal reexposure in processing photographic elements | |
US2515147A (en) | Photographic developer containing an aralkylamine and process of development | |
US3189452A (en) | Color-forming photographic process utilizing a bleach-fix followed by a bleach | |
US3489566A (en) | Magneta color developer solutions | |
US2633422A (en) | Process for making integral color correction masks | |
US3832179A (en) | Inhibition of fog in photographic color development | |
US3667953A (en) | Color photographic positive materials | |
EP0044279A2 (en) | A method of processing monochrome silver halide material | |
EP0547983B1 (en) | Reversal photographic element and processing thereof | |
US3186841A (en) | Method of influencing the gradation of color-photographic printing material | |
US3068097A (en) | Developers for color photography containing sulfite ester polymers | |
US3126282A (en) | Najcoj-hzo | |
US3745008A (en) | Photographic process |