EP0570975A1 - Color photographic element which provides improved magenta image stability - Google Patents
Color photographic element which provides improved magenta image stability Download PDFInfo
- Publication number
- EP0570975A1 EP0570975A1 EP93108277A EP93108277A EP0570975A1 EP 0570975 A1 EP0570975 A1 EP 0570975A1 EP 93108277 A EP93108277 A EP 93108277A EP 93108277 A EP93108277 A EP 93108277A EP 0570975 A1 EP0570975 A1 EP 0570975A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- photographic element
- dye
- epoxide compound
- photographic
- group
- 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.)
- Granted
Links
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
- G03C7/388—Processes for the incorporation in the emulsion of substances liberating photographically active agents or colour-coupling substances; Solvents therefor
- G03C7/3885—Processes for the incorporation in the emulsion of substances liberating photographically active agents or colour-coupling substances; Solvents therefor characterised by the use of a specific solvent
-
- 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
-
- 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
- G03C1/775—Photosensitive materials characterised by the base or auxiliary layers the base being of paper
- G03C1/79—Macromolecular coatings or impregnations therefor, e.g. varnishes
Abstract
Description
- This invention relates to a silver halide photographic element and, more particularly to a color photographic reflection print element that provides improved magenta dye image stability.
- Dyes used in color photographic materials are susceptible to degradation caused by a variety of environmental factors. For example, dyes can be faded by exposure to light of various wavelengths and intensities. In some instances, the fading of dyes by light is exacerbated by the presence of oxygen. Heat and moisture can also have a deleterious effect on the stability of photographic dyes.
- A variety of methods have been proposed to restrict the access of such agents as oxygen and water to photographic images. For example, extruded polyolefin layers to increase the moisture resistance of papers used for photographic prints have been disclosed in U.S. Patent Nos. 3,411,908; 3,630,740; 4,042,398; 4,517,285; and 4,665,014. Resin-coated paper, which consists of a cellulosic fiber paper coated on both sides with polyethylene, is currently the most commonly used support for color photographic reflection prints.
- U.S. Patent No. 4,645,736 discloses a waterproof paper support containing a layer of radiation hardened varnish, and with a polymeric barrier layer such as a polyolefin positioned between the varnish layer and the paper. A waterproof support in which a layer of hardenable acrylic resin is applied between the paper and a polyolefin layer is disclosed in U.S. Patent No. 4,729,945.
- Although resin-coated papers are very impervious to moisture, their oxygen barrier properties are relatively poor, so that dye images on these supports are susceptible to light fading that is promoted by oxygen. U.S. Patent No. 4,283,486 discloses an oxygen impermeable or oxygen barrier layer comprising a vinyl alcohol polymer or copolymer positioned between a paper support and a color image-forming layer. A cover sheet or protective layer to restrict oxygen located above the light-sensitive layer is disclosed in U.S. Patent No. 4,945,025.
- U.S. Patent No. 4,614,681 discloses a polyester film support in which an oxygen barrier layer comprising a copolymer of ethylene and vinyl alcohol is coated on the back side or on both sides of the support. A paper support having an ethylene-vinyl alcohol copolymer oxygen barrier layer on the side on which the image-forming layer is located is disclosed in JP 56/87038.
- A paper support of low air permeability having a coating of a hydrophobic polymer on one or both sides of the paper is disclosed in U.S. Patent No. 4,861,696, which further suggests that a waterproofing agent can be added to the hydrophobic polymer layer.
- EP Application No. 391373 discloses a photographic paper support impregnated through the surface with a low level of a synthetic polymer such as a polyacrylamide or a polyvinyl alcohol as a paper strengthening agent.
- In addition to the fading of dyes by exposure to light, heat, and moisture, a photographic image is susceptible to further degradation resulting from discoloration of white areas, that is, areas of the image where dyes are not present. Discoloration of white areas, like the fading of image dyes, is promoted by exposure to light, both ultraviolet and visible, along with heat and moisture, as well as combinations of these environmental parameters.
- The previously mentioned U.S. Patent No. 4,283,486 reports a reduction of light- and heat-induced discoloration of images produced on a paper support that has a polyvinyl alcohol-containing oxygen barrier layer between the paper and the dye-forming layers. Ultraviolet light (UV) absorbing compounds, especially substituted benzotriazoles, are effective in reducing the discoloration of image white areas caused by exposure to ultraviolet radiation.
- The decomposition of magenta couplers by the action of light, heat, and moisture is a major cause of white area staining. U.S. Patent No. 4,540,657 and JP 62/131259 disclose the use of epoxide compounds as solvents for magenta couplers to reduce light-, heat-, and moisture-induced yellow stain.
- EP Application No. 304067 discloses the use of epoxide solvents for yellow couplers with N-heterocyclic coupling- off groups and reports improvement in the light and dark heat storability of yellow images.
- It is especially desirable to improve the stability of full color photographic prints, composed of yellow, magenta, and cyan dyes, which are usually produced on paper supports and are frequently displayed. Extending the useful life of a color photographic print requires that the dyes be protected against fading by light and other environmental factors, that any fade which does occur be neutral, that is, the decrease in density be approximately the same for each dye, and that staining of white areas be prevented.
- In accordance with the present invention, a silver halide color photographic reflection print element comprises a reflective support and at least one dye-forming layer containing a mixture at a pH of up to about 5 of a silver halide emulsion, a magenta coupler, and an epoxide compound.
- In one embodiment of the invention, the reflective support is a paper support impregnated or coated with an oxygen barrier material. A preferred oxygen barrier material is polyvinyl alcohol.
- In another embodiment of the invention, a layer containing a homopolymer or copolymer of polyvinyl alcohol is interposed between the reflective support and the dye-forming layer.
- In a further embodiment, an ultraviolet light (UV) absorber in an amount of at least 1 mmol/m² is coated above the magenta dye-forming layer.
- The silver halide color photographic reflection print element of the present invention produces a magenta dye image with significantly improved resistance to fading by light and a marked diminution of heat- and moisture-induced staining of white areas. Furthermore, a full color photographic image that is produced by an element of the present invention and contains yellow, magenta, and cyan dyes exhibits, after exposure to light, similar reductions in the densities of its yellow and magenta components in particular. The resulting neutral fade maintains the pleasing appearance of the color photograph and prolongs its useful life.
- In a full color photograph, the fading of the cyan image is caused primarily by the action of light. The degradation of the yellow and magenta images, on the other hand, is the result of the combined effects of exposure to light and oxygen. Therefore, limiting the access of oxygen in the photographic element contributes to the improvement of yellow and magenta dye stability.
- In accordance with the present invention, the reflective support can be a resin-coated paper, or a microvoided oriented polymeric sheet or film disclosed in copending, commonly assigned application, U.S. Serial No. 516,998, filed April 30, 1990, entitled "Photographic Elements Containing Reflective or Diffusely Transmissive Supports," incorporated herein by reference, or a resin-coated microvoided oriented polymeric sheet or film disclosed in co-pending, commonly assigned application, U.S. Serial No 887,710, filed May 22, 1992, entitled "Color Photographic Element with Support Which Provides Improved Dye Stability," incorporated herein by reference.
- In a preferred embodiment, the reflective support is a resin-coated paper that has very low permeability to oxygen. This diminished oxygen-permeability can be attained by inclusion in the support of an oxygen barrier layer containing a homopolymer or copolymer of vinyl alcohol, as disclosed in the previously mentioned U.S. Patent No. 4,283,486, incorporated herein by reference.
- In a more preferred embodiment, the reflective support contains paper that is impregnated with a substance that lowers its oxygen permeability. A preferred oxygen permeability-lowering substance is polyvinyl alcohol, as disclosed in copending, commonly assigned application, U.S. Serial No. 756,262, filed August 19, 1991, entitled "Photographic Paper with Low Oxygen Permeability," incorporated herein by reference.
- In accordance with the present invention, the sheet of paper support can be of any desired basis weight. It is generally preferred that the sheet have a basis weight of between about 122 g/m² (25 lb/1000 ft²) and about 244 g/m² (50 lb/1000 ft²) to provide a conventional feel and handling to the impregnated paper. A heavier weight paper of up to 391 g/m² (80 lb/1000 ft²) may be preferred for display purposes.
- The paper support is impregnated with polyvinyl alcohol, using the procedure described in the previously mentioned application, U.S. Serial No. 756,262, entitled "Photographic Paper with Low Oxygen Permeability." The polyvinyl alcohol utilized can be any polyvinyl alcohol that renders the paper substantially impermeable to oxygen. Polyvinyl alcohol is formed by hydrolysis of vinyl acetate. Polyvinyl alcohol prior to use is soluble in water and available in powder or pellet form. The more fully hydrolyzed polyvinyl alcohols have higher water and humidity resistance. The weight-average molecular weight may vary between above 13,000 and up to 200,000. The higher molecular weight materials have increased water resistance, adhesive strength, and viscosity. A preferred material has been found to be a medium molecular weight polyvinyl alcohol of about 99 percent hydrolysis, as this material provides reduced oxygen permeability of the paper.
- The polyvinyl alcohol polymer is impregnated in any amount that provides substantial oxygen impermeability. Generally it is preferred that the pick-up range be between about 3 and about 12 weight percent of the dry paper weight for an effective barrier to oxygen infiltration and relatively low cost. A pick-up of about 4 to about 9 weight percent is preferred for good oxygen permeability properties at low cost. Impregnation results in a paper that does not have a polyvinyl alcohol layer above the surface but has polyvinyl alcohol concentrated near both surfaces of the paper. It has been found that two applications or passes of the paper in polyvinyl alcohol solution with drying after each pass results in sufficient pick-up of polyvinyl alcohol to provide the oxygen impermeability desired.
- The polyolefin-containing layer is applied to the polyvinyl alcohol-impregnated paper by extrusion from a hot melt as is known from the art, for example, U.S. Patent No. 3,411,908, incorporated herein by reference. In a preferred embodiment of the present invention, the polyolefin is polyethylene and is applied to both sides of the paper support, and the polyethylene layer on the front side also contains 12.5 weight percent anatase TiO₂, 3.0 weight percent ZnO, 0.5 weight percent calcium stearate, and small amounts of antioxidant, colorants and optical brightener. The total amount of coated polyethylene is from about 50 g/m² to about 200 g/m², preferably at least about 70 g/m².
- The polyvinyl alcohol-impregnated and polyethylene-coated paper support can be utilized in the formation of a photographic element of the invention which, after exposing and processing, generates a colored image that is surprisingly stable to light. Furthermore, the image exhibits more nearly neutral fade to light; the image dyes fade at approximately the same rate, thus prolonging the useful lifetime of the print. In a typical color print, the light stabilities of the yellow and magenta image dyes are usually inferior to the light stability of the cyan image dye, leading to an objectionable non-neutral fade of the color print. For color prints produced in accordance with the present invention, however, the light stabilities of the yellow and magenta image dyes are improved substantially, while the light stability of the cyan image dye remains largely unaffected, leading to greater image stability and neutral color fade.
- Magenta image dyes are formed by the reaction of oxidized color developing agents with 2- and 4-equivalent image couplers such as open-chain ketomethylene compounds, pyrazolones, pyrazolotriazoles, pyrazolobenzimidazoles, and indazolones. Typically, such image couplers are ballasted for incorporation in high boiling coupler solvents. Couplers which form magenta dyes upon reaction with oxidized color developing agents are described in such representative patents and publications as: U.S. Patent Nos. 2,600,788; 2,369,489; 2,343,703; 2,311,082; 2,908,573; 3,152,896; 3,519,429; 3,062,653; and T.H. James, editor, The Theory of the Photographic Process, 4th Edition, MacMillan, New York, 1977, pp 356-358, all incorporated herein by reference.
-
- Preferred magenta couplers are 5-pyrazolone compounds. Especially preferred are 1-aryl-3-arylamino-5-pyrazolone compounds.
- As disclosed in the previously mentioned U.S. Patent No. 4,540,657, epoxide compounds containing at least one terminal epoxy group and at least one ester or amide group are useful solvents for magenta couplers in color photographic elements. A color reflection print produced from an element containing a dispersion of a magenta coupler in an epoxide solvent has reduced background stain or discoloration of white areas, which is generated by light, heat, moisture, and combinations thereof.
- The pH of gelatin dispersions of silver halide are typically about 5.6. When a photographic element having a silver halide emulsion that contains a dispersion of a magenta coupler in an epoxide solvent is prepared under these conditions and then kept at elevated temperature and humidity, the magenta coupler is deactivated by interaction with the epoxide solvent, resulting in lowered magenta dye maximum densities upon subsequent photographic processing.
- It has now been unexpectedly found that, if the layer containing the silver halide emulsion, magenta coupler, and epoxide compound is coated at a pH of up to about 5, preferably between about 4.5 and about 5, the activity of the magenta coupler is not degraded during keeping, and a high magenta dye maximum density is obtained upon color photographic processing.
-
- Couplers which form yellow dyes upon reaction with oxidized color developing agents are described in such representative patents and publications as: U.S. Patent Nos. 2,298,443; 2,875,057; 2,407,210; 3,048,194; 3,265,506; 3,447,928; 5,021,333, and The Theory of the Photographic Process, pp 354-356, all incorporated herein by reference.
- In addition, other image couplers which can be used are described in the patents listed in Research Disclosure, December 1989, Item No. 308119, Section VIID, the disclosure of which is incorporated herein by reference.
- Another key element to enhancing the useful lifetime of a color print is the reduction or elimination of the yellow stain which can form on prolonged exposure to light. This can be accomplished by coating an ultraviolet light (UV) absorber in the photographic element. Typically the UV absorbers are substituted phenylbenzotriazoles, which are described in such representative patents as U.S. Patent Nos. 4,383,863; 4,447,511; 4,790,959; 4,752,298; 4,853,471; 4,973,701, incorporated herein by reference. Ultraviolet light absorbers which are liquids are preferred in order to minimize crystallization and surface blooming problems observed with solid absorbers.
- The UV absorber can be coated in gelatin or other protective colloid in one or more layers above the magenta dye-forming layer. The amount of included UV absorber is preferably at least 1 mmol/m², more preferably at least 1.5 mmol/m², and most preferably from about 2.5 to about 4.5 mmol/m².
- Various layers to convert the paper support into a light reflecting print material, such as silver halide emulsion layers, subbing layers, interlayers, and overcoat layers are provided in the photographic element of the invention. The silver halide emulsion employed in the elements of this invention can be either negative-working or positive-working. Suitable emulsions and their preparation are described in sections I and II of Research Disclosure, December 1989, Item No. 308119, sections I and II, the disclosure of which is incorporated herein by reference. The silver halide emulsions employed in the present invention preferably comprise silver chloride grains which are at least 80 mole percent silver chloride and the remainder silver bromide.
-
- A series of magenta dye-forming color photographic elements having the component layers shown in Table 1 below was coated on a resin-coated paper support. The pH of the silver halide emulsion melt containing the magenta coupler dispersion and the gelatin melts for the protective and UV absorber layers was varied from 4.5 to 6.5, using 6N nitric acid. A similar series of coatings with varying melt pH was prepared in which the dibutyl phthalate in the dye-forming layer was replaced at equal weight coverage by the epoxide compound E.
TABLE 1 Layer No. Layer Material Coverage mg/m² 3 Protective Gelatin 1399 Hardener 131 2 UV absorber Gelatin 1076 UV absorber U 129 UV absorber V 732 1 Dye-forming Gelatin 1614 Silver halide 280 Coupler M 430 Stabilizer S 368 Dibutyl phthalate 215 - Samples of each of the series of coatings was incubated in an oven maintained at 49.C and 50% RH for 3 weeks. Duplicate samples were maintained at 0°C for the same period of time. All the samples were simultaneously exposed and processed, using the Kodak Ektacolor RA-4 color development process.
- Maximum densities of magenta dye (green Dmax) were measured for each of the exposed and processed samples, and the differences between the corresponding incubated and non-incubated samples were calculated. Table 2 below compiles the results of these measurements and calculations.
TABLE 2 Element Melt Coating pH Magenta Coupler Solvent Change in Green Dmax After Incubation 1 4.5 dibutyl phthalate -0.04 2 5.0 dibutyl phthalate 0.00 3 5.5 dibutyl phthalate -0.04 4 6.0 dibutyl phthalate -0.03 5 6.5 dibutyl phthalate -0.06 6 4.5 epoxide compound E -0.05 7 5.0 epoxide compound E -0.10 8 5.5 epoxide compound E -0.16 9 6.0 epoxide compound E -0.32 10 6.5 epoxide compound E -0.45 - As shown by the data of Table 2, measured green Dmax values from those elements (1,2,3,4,5) containing dibutyl phthalate in the magenta dye-forming layer were little affected by incubation over the melt coating pH range of 4.5 to 6.5. However those elements (6,7,8,9,10) containing the epoxide compound E showed a lowering of green Dmax for the incubated samples, the magnitude of the loss increasing with higher melt coating pH values and being particularly severe as the melt pH was raised above 5.
- A series of color photographic elements having the component layers shown in Table 3 below was coated on a resin-coated paper support and on a resin-coated support that had been impregnated with 8 weight percent polyvinyl alcohol (based on the weight of the dry starting paper) according to the procedure described in the previously mentioned application, U.S. Serial No. 756,282, entitled "Photographic Paper with Low Oxygen Permeability." The silver halide emulsion melts containing the dye-forming coupler dispersions and the gelatin melts for the protective and UV absorber layers were all adjusted to pH 5.0 with 6N nitric acid.
TABLE 3 Layer No. Layer Material Coverage mg/m² 7 Protective Gelatin 1345 6 UV absorber Gelatin 699 UV absorber W varying 5 Red-sensitive Gelatin 1076 Red-sensitive silver halide* 253 Coupler C 423 Dibutyl phthalate 212 4 UV absorber Gelatin 699 UV absorber W varying 3 Green-sensitive Gelatin 1237 Green-sensitive silver halide* 283 Coupler M 423 Stabilizer S 92 Dibutyl phthalate or epoxide compound E 211 2 Interlayer Gelatin 753 1 Blue-sensitive Gelatin 1506 Blue-sensitive silver halide* 292 Coupler Y 1076 Dibutyl phthalate 269 *Silver halide emulsions are AgBr₁Cl₉₉ - UV absorber W was included in both UV absorber layers in amounts varying from 753-1506 mg/m² (1.92-3.83 mmol/m²). The magenta coupler solvent was varied between dibutyl phthalate and epoxide compound E.
- Samples of the color photographic elements prepared as described were exposed and processed in a standard Kodak Ektacolor RA-4 process. The processed samples were subjected to two test conditions:
- 1. exposure to unfiltered 50 Klux light for 4 weeks, or
- 2. storage at 60°C, 70% RH for 8 weeks.
- Losses of cyan (red fade), magenta (green fade), and yellow (blue fade) dyes from a neutral image area and increases in yellow stain (printout ΔDmin) in a white area were measured after test condition 1, and increases in yellow stain (yellowing ΔDmin) in a white area resulting from the combined effects of heat and moisture were measured after test condition 2. The results of these measurements are compiled in Table 4.
TABLE 4 Element Paper Support UV Absorber W Coverage in each UV absorber layer mg/m² (mmol/m²) Magenta Coupler Solvent Dye Fade from neutral image 50 Klux for 4 weeks Printout ΔDmin 50 Klux for 4 weeks Yellowing ΔDmin 60°C, 70% RH 8 weeks 1 Resin-coated 753 (1.92) Dibutyl phthalate Red -0.27 0.22 0.15 Green -0.28 Blue -0.13 2 Resin-coated 1506 (3.83) Dibutyl phthalate Red -0.27 0.06 0.14 Green -0.28 Blue -0.13 3 Polyvinyl alcohol-impregnated resin-coated 861 (2.19) Dibutyl phthalate Red -0.24 0.18 0.15 Green -0.17 Blue -0.13 4 Polyvinyl alcohol-impregnated resin-coated 1442 (3.67) Dibutyl phthalate Red -0.14 0.03 0.15 Green -0.16 Blue -0.15 5 Polyvinyl alcohol-impregnated resin-coated 1442 (3.67) Epoxide compound E Red -0.14 0.04 0.08 Green -0.16 Blue -0.15 - Element 1, which contained the magenta coupler dispersed in dibutyl phthalate, 753 mg/m² (1.92 mmol/m²) of UV absorber in each UV absorber layer, and a resin-coated paper support, showed high light fade of the magenta dye in a neutral image area and also gave a large increase in yellow stain in white areas both after light exposure (test condition 1) and after storage at elevated temperature and humidity (test condition 2).
- Element 2, which differed from element 1 in containing a higher coverage of UV absorber (1506 mg/m², 3.83 mmol/m²) in each UV absorber layer, showed a large decrease in light-induced staining (printout WDmin) of white areas.
- The coated component layers of element 3 were similar to those of element 1, but they were coated on a polyvinyl alcohol-impregnated paper support. The magenta dye light fade of element 3 in a neutral image area was considerably improved relative to that measured for element 1, but yellow stain produced by light, heat and moisture remained high.
- Element 4, which differed from element 3 in containing a high coverage of UV absorber (1442 mg/m², 3.67 mmol/m²) in each UV absorber layer, showed low and equal tight fade of all three dyes in a neutral image area ad low light-induced yellow stain in white areas, but the yellowing stain after storage at 60°C, 70% RH remained high.
- Element 5 was similar to element 4, except that the magenta coupler solvent was, in accordance with the present invention, an epoxide compound. The low, neutral light fade ad low printout measured for element 4 were maintained in clement 5, which, in addition, exhibited significantly reduced yellowing in the white areas. This demonstrates the advantage, in accordance with the present invention, of a photographic reflection print element containing an oxygen barrier material, a epoxide compound in the magenta dye-forming layer at a pH of up to about 5, and a amount of ultraviolet light absorber of at least 2 mmol/m², ad preferably more than 3 mmol/m², in each UV absorber layer.
Claims (10)
- A silver halide color photographic reflection print element comprising: a reflective support; and at least one dye-forming layer containing a mixture at a pH of up to about 5 of a silver halide emulsion, a magenta coupler, and an epoxide compound.
- A photographic element of Claim 1 wherein said reflective support is a paper support impregnated or coated with an oxygen barrier material.
- A photographic element of Claim 2 wherein said oxygen gas transmission rate-reducing substance is polyvinyl alcohol.
- A photographic element of Claim 3 further comprising a second polyolefin-containing layer on said support on the side opposite to that which bears said dye-forming layer and a layer that contains an ultraviolet light absorber overlying said dye-forming layer.
- A photographic element of Claim 1 wherein said epoxide compound has at least one terminal epoxy group and at least one ester or amide group.
- A photographic element of Claim 5, wherein said epoxide compound has the formula:
- A photographic element of Claim 7, wherein A¹ is a benzene ring, n is 2, and each L¹ is -COO(CH₂)₉.
- A photographic element of Claim 1 wherein the weight ratio of said epoxide compound to said magenta coupler is from about 0.1:1 to about 2:1.
- A photographic element of Claim 4 wherein said paper support contains from about 3 to about 12 weight percent polyvinyl alcohol.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US887294 | 1986-07-18 | ||
US88729492A | 1992-05-22 | 1992-05-22 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0570975A1 true EP0570975A1 (en) | 1993-11-24 |
EP0570975B1 EP0570975B1 (en) | 1998-09-16 |
Family
ID=25390849
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP19930108277 Expired - Lifetime EP0570975B1 (en) | 1992-05-22 | 1993-05-21 | Color photographic element which provides improved magenta image stability |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP0570975B1 (en) |
JP (1) | JPH0651471A (en) |
DE (1) | DE69321027T2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6077642A (en) * | 1996-04-22 | 2000-06-20 | Fuji Photo Film Co., Ltd. | Recording material |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2059614A (en) * | 1979-10-02 | 1981-04-23 | Fuji Photo Film Co Ltd | Silver halide colour photographic lightsensitive material |
JPS62253154A (en) * | 1986-04-10 | 1987-11-04 | Fuji Photo Film Co Ltd | Preparation of silver halide photographic sensitive material |
EP0331004A1 (en) * | 1988-03-01 | 1989-09-06 | EASTMAN KODAK COMPANY (a New Jersey corporation) | Color photographic reflection print material with improved keeping properties |
US5047315A (en) * | 1987-09-11 | 1991-09-10 | Fuji Photo Film Co., Ltd. | Silver halide color photographic material |
-
1993
- 1993-05-19 JP JP5116788A patent/JPH0651471A/en active Pending
- 1993-05-21 EP EP19930108277 patent/EP0570975B1/en not_active Expired - Lifetime
- 1993-05-21 DE DE1993621027 patent/DE69321027T2/en not_active Expired - Fee Related
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2059614A (en) * | 1979-10-02 | 1981-04-23 | Fuji Photo Film Co Ltd | Silver halide colour photographic lightsensitive material |
JPS62253154A (en) * | 1986-04-10 | 1987-11-04 | Fuji Photo Film Co Ltd | Preparation of silver halide photographic sensitive material |
US5047315A (en) * | 1987-09-11 | 1991-09-10 | Fuji Photo Film Co., Ltd. | Silver halide color photographic material |
EP0331004A1 (en) * | 1988-03-01 | 1989-09-06 | EASTMAN KODAK COMPANY (a New Jersey corporation) | Color photographic reflection print material with improved keeping properties |
Non-Patent Citations (1)
Title |
---|
PATENT ABSTRACTS OF JAPAN vol. 11, no. 350 (P-637)(2797) 17 November 1987 & JP-A-62 129 847 ( KONISHIROKU ) 12 June 1987 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6077642A (en) * | 1996-04-22 | 2000-06-20 | Fuji Photo Film Co., Ltd. | Recording material |
Also Published As
Publication number | Publication date |
---|---|
JPH0651471A (en) | 1994-02-25 |
DE69321027T2 (en) | 1999-05-12 |
EP0570975B1 (en) | 1998-09-16 |
DE69321027D1 (en) | 1998-10-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4383863A (en) | 2-[2-Hydroxy-3,5-di-tert-octylphenyl]-2H-benzotriazole in stabilized photographic compositions | |
US4195999A (en) | Silver halide photographic material containing ultraviolet light absorbing agent | |
CA1270839A (en) | Liquid 2-(2-hydroxy-3-higher branched alkyl-5-methyl- phenyl)-2h-benzotriazole mixtures, stabilized compositions and processes for preparing liquid mixtures | |
US3705805A (en) | Photographic layers containing compounds which absorb ultraviolet light | |
US4009038A (en) | Silver halide color photographic materials | |
EP0210409B1 (en) | 3-aminoallylidenemalononitrile uv-absorbing compounds and photographic elements containing them | |
US5290671A (en) | Color photographic element providing improved dye stability | |
US3794493A (en) | Photographic layers which contain uv-absorbers | |
DE3038053A1 (en) | COLOR PHOTOGRAPHIC, LIGHT-SENSITIVE MATERIAL | |
US3725072A (en) | Color photographic light-sensitive materials containing a novel yellow-forming coupler | |
EP0331004A1 (en) | Color photographic reflection print material with improved keeping properties | |
US3650752A (en) | Whitened photographic printing paper | |
EP0570975B1 (en) | Color photographic element which provides improved magenta image stability | |
US5610000A (en) | 2'-hydroxyphenyl benzotriazole based UV absorbing polymers and photographic elements containing them | |
US4163671A (en) | Silver halide photographic material containing ultraviolet light absorbing agent | |
GB2043931A (en) | Silver halide colour photographic lightsensitive material | |
US5254450A (en) | Hydrophobically substituted amylose starch-sized photographic paper support and photographic element containing same | |
US4447511A (en) | 2-[2-Hydroxy-3,5-di-tert-octylphenyl]-2H-benzotriazole in stabilized photographic compositions | |
US5429913A (en) | Photographic coupler compositions containing ballasted alcohols and methods | |
US4935321A (en) | Photographic recording material comprising a dye image-forming compound | |
EP0509311A1 (en) | Photographic coupler compositions containing ballasted sulfoxides or sulfones and methods for the formation of colour images | |
US5476756A (en) | Color photographic element with improved resistance to thermal and photochemical yellowing | |
US4052216A (en) | Color photographic material containing a hydroxyindane | |
CA1122842A (en) | Color photographic light-sensitive material containing 2,5-bis (1,1'-dimethylbutyl) hydroquinone and a 3-anilino 5-pyrazolone magenta coupler | |
US6017689A (en) | Color photographic silver halide material |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): BE CH DE FR GB IT LI NL |
|
17P | Request for examination filed |
Effective date: 19940505 |
|
GRAG | Despatch of communication of intention to grant |
Free format text: ORIGINAL CODE: EPIDOS AGRA |
|
GRAG | Despatch of communication of intention to grant |
Free format text: ORIGINAL CODE: EPIDOS AGRA |
|
GRAH | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOS IGRA |
|
17Q | First examination report despatched |
Effective date: 19980130 |
|
RBV | Designated contracting states (corrected) |
Designated state(s): DE FR GB |
|
GRAH | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOS IGRA |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): DE FR GB |
|
REF | Corresponds to: |
Ref document number: 69321027 Country of ref document: DE Date of ref document: 19981022 |
|
ET | Fr: translation filed | ||
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
26N | No opposition filed | ||
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 20000504 Year of fee payment: 8 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 20010404 Year of fee payment: 9 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20010530 Year of fee payment: 9 |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: IF02 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20020131 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20020521 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20021203 |
|
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 20020521 |