US3356502A - Ammonium or alkali metal thiocyanate aqueous rinse solution for stabilized silver photographic images - Google Patents

Ammonium or alkali metal thiocyanate aqueous rinse solution for stabilized silver photographic images Download PDF

Info

Publication number
US3356502A
US3356502A US459802A US45980265A US3356502A US 3356502 A US3356502 A US 3356502A US 459802 A US459802 A US 459802A US 45980265 A US45980265 A US 45980265A US 3356502 A US3356502 A US 3356502A
Authority
US
United States
Prior art keywords
print
stabilizing
ammonium
alkali metal
treatment
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
Application number
US459802A
Inventor
Nasu Kintaro
Tajima Tatsuya
Kano Takao
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Fujifilm Holdings Corp
Original Assignee
Fuji Photo Film Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Fuji Photo Film Co Ltd filed Critical Fuji Photo Film Co Ltd
Application granted granted Critical
Publication of US3356502A publication Critical patent/US3356502A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C5/00Photographic processes or agents therefor; Regeneration of such processing agents
    • G03C5/26Processes using silver-salt-containing photosensitive materials or agents therefor
    • G03C5/38Fixing; Developing-fixing; Hardening-fixing
    • G03C5/39Stabilising, i.e. fixing without washing out

Definitions

  • This invention relates to an improved silver halide photographic method. More particularly, the invention relates to a process for the rapid treatment of a photographic material to give improved printed images.
  • a photographic print is, after being developed by a conventional method, treated with a solution of a stabilizing agent, such as ammonium thiocyanate, and is dried immediately without being rinsed.
  • a stabilizing agent such as ammonium thiocyanate
  • a fixing procedure is unnecessary and therefore the period of'time for treating light-exposed photographic materials can be reduced.
  • Such various rapid treatments for photographic materials are described in, e.g., H. D.'Russell, B. C.'Yackel and G. S. Bruce; Photographic Science and Technical Journal; August, pp. 59 62 (1950), Broughton et al., US. Patent 2,614,927 (published on Oct. 21, 1952), and Brice, U.S. Patent 2,448,857 (published on Sept. 7, 1948).
  • the stabilizing agent used generally in such rapid treating processes is a compound having a double-bonded sulfur or an SH linkage, for example, alkali metal thiocyanate, ammonium thiocyanate, an alkali thiosulfate, ammonium"thiosulfate, thiourea, and thioglycol.
  • the stabilizing treatment usingsuch a stabilizing agent makes the rapid treatment possible but is accompanied with many defects in'the treated prints. For example, since the above-mentioned stabilizing agent is used in an amount considerably larger than the theoretical amount necessary to secure the light-stability of thus stabilized print and since'the stabilizing agent is hygroscopic, complete drying of the print is difficult and the surface of the print is sticky.
  • the stabilizing agent gradually oxidizes metallic silver of the images in the print into a silver complex salt, the image density is reduced or vanished, and the color tone of the image is changed from black to brown oryellovv. Such a fading phenomenon is liable to occur in particular when the print is stored under high'humidity. Further, if a photosensitive material is exposedto light when the reaction between the undeveloped silver halide and 'the stabilizing agent is not finished",- photo-decomposition of the non-stabilized silver halide occurs, which stains the white portions and transparent portions of the treated photosensitive material.
  • anobject of this invention is to provide a process for improving the quality of prints by removing th e above-mentioned general defects in the rapid treatment system.
  • the first object of this invention is to reduce the hygroscopicity of the print and to remove the stickiness of the surface of the print.
  • the second object of this invention is to reduce the density of salts in the treated photosensitive layer of the print and to enable ferrotype finishing.
  • ferrotype finishing i.e., a treatment for smoothing the surface of the print by pressing the print into contact with a heated metal plate
  • ferrotyped print loses gradually its luster, it can be adopted suitably and 3,356,502 Patented Dec. 5, 1967 effectively in the process of the present invention.
  • the third object of this invention is to improve the whiteness of the white portions and the transparency of the transparent portions of the treated print and to prevent discoloring of the treated print into yellow or orange caused by exposing it to a light which contains a light near the ultraviolet range, e.g., to sunlight.
  • the stickiness of the surface layer of the print is almostcoinpletely removed and has the same surface properties as that of a print subjected to fixing and rinsing treatments.
  • This enables the print to be subjected to ferrotype finishing, and, after ferrotype finishing, the print treated by the process of this invention can keep its luster for a long period of time.
  • a fluorescent whitening agent or a noble metal salt, organo-mercapto compound or thiosulfate shown in the above-mentioned patents into the second stabilizing bath of this invention, the fading of the silver image and the Whitness can be further improved.
  • the stabilization process of this invention is conducted substantially in two stabilizing baths, but if only the period of time for the first stabilization is prolonged, the print can be stabilized and the similar effect as that of this invention can be obtained by only, the first stabilizing bath. That is, by prolonging the treating period, the effects for enabling the application of ferrotype finishing and preventing yellowing of the print by ultraviolet rays can be obtained. However, in the latter case, the stabilization period is prolonged in vain when the effects by the process of this invention are not desired, which is undesirable in a point of a socalled rapid treatment, and
  • an adaptable treating system can be obtained with or without applying ferrotype finishing (to the surface or the backside surface) according to purposes to be required.
  • ferrotype finishing to the surface or the backside surface
  • the use of a suitable diluted one-solution stabilizing system may be regarded as an embodiment of this invention.
  • Example 1 A gelatin-silver chloride emulsion containing hydroquinone was applied on a baryta paper to form a photosensitive paper, which was then, after being exposed and developed, treated by a stabilizing solution having the following composition;
  • the treatment was carried out at room temperature, the development and the stabilization treatment was finished sufficiently in about seconds.
  • the stabilized print was obtained in a semi-dried state, the surface of the print lacked the luster of a ferrotype-finished print, although the treated print could be considered sufficiently satisfactory.
  • the thus treated print was immersed for about 3 minutes in an aqueous solution (the second stabilizing bath) prepared by diluting the first stabilizing solution with water to 6 times its original volume, the excess solution was lightly wiped away, and the print was processed on a ferrotype machine.
  • a finished print was obtained which was by no means inferior to a print subjected to fixing, rinsing and ferrotype finishing.
  • the second stabilizing bath greatly improved the quality of the print subjected to only one stabilizing bath.
  • the results of measuring the luster of the print subjected to the second stabilizing treatment and the print subjected to the usual one-bath stabilizing treatment are shown in the following table.
  • the measurement was made by using a luster meter with the angle of incidence 60.
  • Example 2 When the procedure of Example 1 was used with an aqueous solution of 4 weight percent of potassium thiocyanate as the second stabilizing bath, a print having the same features as in the case of Example 1 was obtained.
  • Example 4 A photosensitive paper prepared by applying on a baryta paper a gelatin-silver bromide emulsion containing a small amount of the bromide was light-exposed and developed by a surface coating process with a developing solution having the following composition:
  • the developed photosensitive paper was then treated with a stabilizing solution (1st stabilizing bath) having the following composition:
  • the first stabilizing treatment was carried out as in Example 1, the thus treated sensitive paper was immersed in a second stabilizing bath containing 4 weight percent of ammonium thiocyanate and 0.1 weight percent of a fluorescent whitening agent such as Whitex 3B (trade name by the Sumitomo Chemical Industry Co.) for 3 minutes and then was subjected to ferrotype finishing.
  • spectral reflectivity curves of a print (II) prepared with the second stabilization treatment of this invention and a comparative print (I) prepared with no second stabilization treatment are shown in the accompanying drawings.
  • FIG. 1 there are no large differences between the print (II) and the comparative print (1) directly after ferrotype finishing, but as shown in FIG. 2, the reduction (yellowing) of the whiteness of the print (II) when exposed to daylight for about 24 hours is substantially less than that of the print (I). Since the whitening effect of a fluorescent whitening agent does not show up in the curves, the practical whiteness of the print (II) is better than that shown in the figures.
  • Example 5 The composition of the second stabilizing bath in Example 4 is replaced with 5 weight percent of potassium thiocyanate and 0.5 weight percent of Whitex 3B.
  • the same effect as in Example 4 was obtained with an immersion period of 1 minute. Further, the deterioration of the second stabilizing bath caused by treating many prints was less than in the case of the second bath of Example 4.
  • Example 6 By replacing the composition of the second stabilizing bath in Example 4 with 4 weight percent of amonium thiocyanate and 6 Weight percent of potassium metabisulfite, almost the same results as in Examiple 4 were obtained with an immersion period of 5 minutes. In this case, a fluorescent whitening effect could not be obtained but other properties of the obtained print were almost the same as those in Example 4.
  • Example 7 In the case of a low-luster paper, such as where the surface of the photosensitive paper in Examples 1-6 was matted or semi-matted, and in the case of a paper having a specific surface property, such as a silk surface or a fine-grained surface, the first and the second stabilization treatments were carried out as in the above examples except that ferrotype finishing was applied to the back side of the paper. By these treatments, a print having reduced yellowing by daylight and a reduced surface stickiness was obtained.
  • a low-luster paper such as where the surface of the photosensitive paper in Examples 1-6 was matted or semi-matted
  • a paper having a specific surface property such as a silk surface or a fine-grained surface
  • the developed material is stabilized with a stabilizing bath containing at least one compound selected from the group consisting of ammonium thiocyanate and an alkali metal thiocyanate, and is then dried, the improvement which comprises immers- UNITED STATES PATENTS 10/1952 Broughton et al. 966l OTHER REFERENCES John, D. H. 0., et al.: Photographic Chemistry, New York, Reinhold Publishing Corporation, 1963, page 157.

Landscapes

  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Silver Salt Photography Or Processing Solution Therefor (AREA)
  • Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)

Description

Dec. 5, 1967 AMMONIUM on ALKALI METAL THIOCYANATE AQUEOUS RINSE SOLUTION FOR STABILIZED SILVER PHOTOGRAPHIC IMAGES REFLECTION ("/o) IIO- REFLECTION (f/o) KINTARO NASU ETAL 3,356,502
Filed May 28,, 1965 500 600 WAVE LENGTH ('mp.)
500 600 WAVE LE NGTH (TTI'L) F I G. 2
fluafwo can! We United States Patent Ja an p Filed'May 28, 1965, Ser. No. 459,802 Claims priority, application Japan, June 25, 1964,
- 7 v 39/3s,74s
1 Claim. (Cl. 96-50) This invention relates to an improved silver halide photographic method. More particularly, the invention relates to a process for the rapid treatment of a photographic material to give improved printed images.
A rapid treatment system for photographic materials to form silver images without the necessity of a so-called fixing and rinsing treatment has been already known.
In such a system, a photographic print is, after being developed by a conventional method, treated with a solution of a stabilizing agent, such as ammonium thiocyanate, and is dried immediately without being rinsed. In this treatment, a fixing procedure is unnecessary and therefore the period of'time for treating light-exposed photographic materials can be reduced. Such various rapid treatments for photographic materials are described in, e.g., H. D.'Russell, B. C.'Yackel and G. S. Bruce; Photographic Science and Technical Journal; August, pp. 59 62 (1950), Broughton et al., US. Patent 2,614,927 (published on Oct. 21, 1952), and Brice, U.S. Patent 2,448,857 (published on Sept. 7, 1948).
The stabilizing agent used generally in such rapid treating processes is a compound having a double-bonded sulfur or an SH linkage, for example, alkali metal thiocyanate, ammonium thiocyanate, an alkali thiosulfate, ammonium"thiosulfate, thiourea, and thioglycol. The stabilizing treatment usingsuch a stabilizing agent makes the rapid treatment possible but is accompanied with many defects in'the treated prints. For example, since the above-mentioned stabilizing agent is used in an amount considerably larger than the theoretical amount necessary to secure the light-stability of thus stabilized print and since'the stabilizing agent is hygroscopic, complete drying of the print is difficult and the surface of the print is sticky. Moreover, since the stabilizing agent gradually oxidizes metallic silver of the images in the print into a silver complex salt, the image density is reduced or vanished, and the color tone of the image is changed from black to brown oryellovv. Such a fading phenomenon is liable to occur in particular when the print is stored under high'humidity. Further, if a photosensitive material is exposedto light when the reaction between the undeveloped silver halide and 'the stabilizing agent is not finished",- photo-decomposition of the non-stabilized silver halide occurs, which stains the white portions and transparent portions of the treated photosensitive material.
Therefore, anobject of this invention is to provide a process for improving the quality of prints by removing th e above-mentioned general defects in the rapid treatment system. Namely, the first object of this invention is to reduce the hygroscopicity of the print and to remove the stickiness of the surface of the print. Further, the second object of this invention is to reduce the density of salts in the treated photosensitive layer of the print and to enable ferrotype finishing. While ferrotype finishing, i.e., a treatment for smoothing the surface of the print by pressing the print into contact with a heated metal plate, can not be applied in conventional stabilizing treatments, or, if it is possible, the ferrotyped print loses gradually its luster, it can be adopted suitably and 3,356,502 Patented Dec. 5, 1967 effectively in the process of the present invention. Still further, the third object of this invention is to improve the whiteness of the white portions and the transparency of the transparent portions of the treated print and to prevent discoloring of the treated print into yellow or orange caused by exposing it to a light which contains a light near the ultraviolet range, e.g., to sunlight.
These objects can be achieved by the process of this invention, by treating a photographic layer stabilized with ammonium thiocyanate and/or an alkali metal thiocyanate for a short period of time, preferably, for 1-10 minutes with a solution containing same or different thiocyanate compounds in a concentration of 1-15 percent by weight, that is, a concentration lower than that of the solution containing the thiocyanate compound or compounds used for the stabilization. If the concentration of the solution is lower than 1%, the thiocyanate or thiocyanates in the photographic layer flow out of the layer, which makes the stabilization insufficient. On the other hand, if the concentration is above 15%, the amount of the thiocyanates in the photographic layer is increased to an amount more than is necessary and the metallic silver of the image in the print is easily attacked by the compounds.
Hitherto, it was an object of the rapid treatment to finish the development and the stabilization within at least 1 minute, and usually in a short period less than 10 seconds. Hence, the concentration of the stabilizing agent was increased as high as possible. But almost all of the practical stabilizing agents have extremely high solubilities, and while the stabilization rate was high, the density of salts in the photographic layer of the print was also high, resulting in increasing the hygroscopicity and stickiness of the layer as well as in causing fading of the images.
As countermeasures, there have already been known the addition of a noble metal salt and an organo-mercapto compound, the use of a thiosulfate together with the thiocyanate (E. T. Smith and G. W. W. Stevens; US. Patent 3,132,943, published on May 12, 1964), and the addition of a sulfite, bisulfite or metabisulfite of an alkali metal or ammonium. However, while fading of the silver image and discoloring of the white portions and transparent portions may be prevented by such treatments, the effect is not complete and the stickiness of the surface of the emulsion layer of the print is usually hardly reduced.
By the process of the present invention, the stickiness of the surface layer of the print is almostcoinpletely removed and has the same surface properties as that of a print subjected to fixing and rinsing treatments. This enables the print to be subjected to ferrotype finishing, and, after ferrotype finishing, the print treated by the process of this invention can keep its luster for a long period of time. Further, by adding a fluorescent whitening agent or a noble metal salt, organo-mercapto compound or thiosulfate shown in the above-mentioned patents into the second stabilizing bath of this invention, the fading of the silver image and the Whitness can be further improved. p
The stabilization process of this invention is conducted substantially in two stabilizing baths, but if only the period of time for the first stabilization is prolonged, the print can be stabilized and the similar effect as that of this invention can be obtained by only, the first stabilizing bath. That is, by prolonging the treating period, the effects for enabling the application of ferrotype finishing and preventing yellowing of the print by ultraviolet rays can be obtained. However, in the latter case, the stabilization period is prolonged in vain when the effects by the process of this invention are not desired, which is undesirable in a point of a socalled rapid treatment, and
by carrying out the stabilizing treatment in a two-bath system as in the case of this invention, an adaptable treating system can be obtained with or without applying ferrotype finishing (to the surface or the backside surface) according to purposes to be required. Of course, the use of a suitable diluted one-solution stabilizing system may be regarded as an embodiment of this invention.
Further understanding of the novel process of this invention can be obtained from the following examples, which disclose the preferred modes of this invention.
Example 1 A gelatin-silver chloride emulsion containing hydroquinone was applied on a baryta paper to form a photosensitive paper, which was then, after being exposed and developed, treated by a stabilizing solution having the following composition;
Water 50 c.) ml 500 Ammonium thiocyanate g 250 Sodium bisulfite g 70 Sulfuric acid monomethyl-p-aminophenol g 2 l-phenyl-S-thiol tetrasol (1% alcohol solution) ml 60 C0804 g 0.3
Water to make 1 liter.
When the treatment was carried out at room temperature, the development and the stabilization treatment was finished sufficiently in about seconds. As the stabilized print was obtained in a semi-dried state, the surface of the print lacked the luster of a ferrotype-finished print, although the treated print could be considered sufficiently satisfactory.
The thus treated print was immersed for about 3 minutes in an aqueous solution (the second stabilizing bath) prepared by diluting the first stabilizing solution with water to 6 times its original volume, the excess solution was lightly wiped away, and the print was processed on a ferrotype machine. A finished print was obtained which was by no means inferior to a print subjected to fixing, rinsing and ferrotype finishing. Thus, the second stabilizing bath greatly improved the quality of the print subjected to only one stabilizing bath.
The results of measuring the luster of the print subjected to the second stabilizing treatment and the print subjected to the usual one-bath stabilizing treatment are shown in the following table. The measurement was made by using a luster meter with the angle of incidence 60.
Directly After 2 after weeks from ferrotype ferrotype finishing finishing Treated by only the 1st stabilizing bath 65 59 Immersed in the 2nd stabilizing b'ath alterthe 1st stabilizing treatment 100 98 The use of a second stabilizing bath not only results in a print of higher luster after ferrotype-finishing, but also significantly decreases the loss in luster occurring after storage at room temperature and normal humidity, as compared to the use of the usual single-bath stabilization.
Example 2 Example 3 When the procedure of Example 1 was used with an aqueous solution of 4 weight percent of potassium thiocyanate as the second stabilizing bath, a print having the same features as in the case of Example 1 was obtained.
Example 4 A photosensitive paper prepared by applying on a baryta paper a gelatin-silver bromide emulsion containing a small amount of the bromide was light-exposed and developed by a surface coating process with a developing solution having the following composition:
Sodium hydroxide 22.5 Sodium sulfiate (anhydrous) 8O Hydroquinone 36 Potassium bromide 0.5 Pyrazone 2 Water to make 1 liter.
The developed photosensitive paper was then treated with a stabilizing solution (1st stabilizing bath) having the following composition:
Potassium thiocyanate g 300 Potassium metabisulfite g 50 Sodium sulfite (anhydrous) g 15 Glacial acetic acid cc 40 Sodium phosphate (Nag-IP0 g- 15 Water to make 1 liter.
The first stabilizing treatment was carried out as in Example 1, the thus treated sensitive paper was immersed in a second stabilizing bath containing 4 weight percent of ammonium thiocyanate and 0.1 weight percent of a fluorescent whitening agent such as Whitex 3B (trade name by the Sumitomo Chemical Industry Co.) for 3 minutes and then was subjected to ferrotype finishing. By this treatment, a print having the features as in Example 1, as well as having extremely good whiteness and a sharp image contrast, was obtained.
In order to clarify the effect of the process of this invention, spectral reflectivity curves of a print (II) prepared with the second stabilization treatment of this invention and a comparative print (I) prepared with no second stabilization treatment are shown in the accompanying drawings. As shown in FIG. 1, there are no large differences between the print (II) and the comparative print (1) directly after ferrotype finishing, but as shown in FIG. 2, the reduction (yellowing) of the whiteness of the print (II) when exposed to daylight for about 24 hours is substantially less than that of the print (I). Since the whitening effect of a fluorescent whitening agent does not show up in the curves, the practical whiteness of the print (II) is better than that shown in the figures.
Example 5 The composition of the second stabilizing bath in Example 4 is replaced with 5 weight percent of potassium thiocyanate and 0.5 weight percent of Whitex 3B. By using the above stabilizing bath, the same effect as in Example 4 was obtained with an immersion period of 1 minute. Further, the deterioration of the second stabilizing bath caused by treating many prints was less than in the case of the second bath of Example 4.
Example 6 By replacing the composition of the second stabilizing bath in Example 4 with 4 weight percent of amonium thiocyanate and 6 Weight percent of potassium metabisulfite, almost the same results as in Examiple 4 were obtained with an immersion period of 5 minutes. In this case, a fluorescent whitening effect could not be obtained but other properties of the obtained print were almost the same as those in Example 4.
Example 7 In the case of a low-luster paper, such as where the surface of the photosensitive paper in Examples 1-6 was matted or semi-matted, and in the case of a paper having a specific surface property, such as a silk surface or a fine-grained surface, the first and the second stabilization treatments were carried out as in the above examples except that ferrotype finishing was applied to the back side of the paper. By these treatments, a print having reduced yellowing by daylight and a reduced surface stickiness was obtained.
We claim:
In a process for the rapid treatment of a silver halide photographic material wherein the silver halide photographic material is developed, the developed material is stabilized with a stabilizing bath containing at least one compound selected from the group consisting of ammonium thiocyanate and an alkali metal thiocyanate, and is then dried, the improvement which comprises immers- UNITED STATES PATENTS 10/1952 Broughton et al. 966l OTHER REFERENCES John, D. H. 0., et al.: Photographic Chemistry, New York, Reinhold Publishing Corporation, 1963, page 157.
NORMAN G. TORCHIN, Primary Examiner.
C. E. DAVIS, Assistant Examiner.
US459802A 1964-06-25 1965-05-28 Ammonium or alkali metal thiocyanate aqueous rinse solution for stabilized silver photographic images Expired - Lifetime US3356502A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3574864 1964-06-25

Publications (1)

Publication Number Publication Date
US3356502A true US3356502A (en) 1967-12-05

Family

ID=12450422

Family Applications (1)

Application Number Title Priority Date Filing Date
US459802A Expired - Lifetime US3356502A (en) 1964-06-25 1965-05-28 Ammonium or alkali metal thiocyanate aqueous rinse solution for stabilized silver photographic images

Country Status (6)

Country Link
US (1) US3356502A (en)
BE (1) BE665963A (en)
CH (1) CH447810A (en)
DE (1) DE1472896B2 (en)
GB (1) GB1061606A (en)
NL (1) NL146610B (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3663227A (en) * 1968-11-29 1972-05-16 Fuji Photo Film Co Ltd Rapid stabilization process for photographic silver halide materials
US4336324A (en) * 1980-06-18 1982-06-22 Konishiroku Photo Industry Co., Ltd. Method for the processing of silver halide color photographic light-sensitive materials
US4778748A (en) * 1984-07-13 1988-10-18 Konishiroku Photo Industries, Co., Ltd. Method for processing light-sensitive silver halide color photographic material

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3436862A1 (en) * 1984-10-08 1986-04-10 Tetenal Photowerk GmbH & Co, 2000 Norderstedt Process for stabilising a colour-photographic material, and a stabilising bath for use in this process

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2614927A (en) * 1949-06-01 1952-10-21 Eastman Kodak Co Rapid processing of photographic materials

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2614927A (en) * 1949-06-01 1952-10-21 Eastman Kodak Co Rapid processing of photographic materials

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3663227A (en) * 1968-11-29 1972-05-16 Fuji Photo Film Co Ltd Rapid stabilization process for photographic silver halide materials
US4336324A (en) * 1980-06-18 1982-06-22 Konishiroku Photo Industry Co., Ltd. Method for the processing of silver halide color photographic light-sensitive materials
US4778748A (en) * 1984-07-13 1988-10-18 Konishiroku Photo Industries, Co., Ltd. Method for processing light-sensitive silver halide color photographic material

Also Published As

Publication number Publication date
DE1472896B2 (en) 1977-05-12
CH447810A (en) 1967-11-30
GB1061606A (en) 1967-03-15
NL6508188A (en) 1965-09-27
NL146610B (en) 1975-07-15
BE665963A (en) 1965-10-18
DE1472896A1 (en) 1968-11-28

Similar Documents

Publication Publication Date Title
US2453346A (en) Stabilization of processed photographic emulsions to high temperatures and humidities
DE69220866T2 (en) Development of color photographic recording material
DE2247582A1 (en) PROCESS FOR DEVELOPING COLOR PHOTOGRAPHICAL MATERIALS
US3356502A (en) Ammonium or alkali metal thiocyanate aqueous rinse solution for stabilized silver photographic images
US2339309A (en) Photographic reducing composition and process
US4040837A (en) Photographic bleach-fixer
US3212895A (en) Stability of rapid-processed photographic materials
US1930140A (en) Acid hardening fixing bath
US1973466A (en) Photographic developing solutions
US5026629A (en) Fixing bath for black and white photographic elements
US5464728A (en) Method of bleaching and fixing a color photographic element containing high iodine emulsions
CA1114667A (en) Method of post-process intensification of images on photographic films and plates
JPS59184345A (en) Method for processing color photographic sensitive silver halide material
DE2406515C3 (en) Photographic material for use in direct positives
JPS62257150A (en) Stabilization of silver image generated photographically
US5262285A (en) Methods and compositions for retouching film images
US3259497A (en) Photographic color reversal process
US2929709A (en) Photographic process
DE2309526A1 (en) METHOD FOR RAPID PROCESSING OF SILVER BLEACHING MATERIALS
US3707379A (en) Process for the formation of photographic images
DE69308016T2 (en) PHOTOGRAPHIC PROCESSING PROCESS AND USE OF PHOTOGRAPHIC PRODUCTS WITH A FINE GRAIN Liner
US4194911A (en) Inhibitor removing bath for direct positive color photographic development
US2459136A (en) Dry developing negative
Pope Formation of silver sulfide in the photographic image during fixation
JPS63136043A (en) Method for processing silver halide photographic sensitive material