EP0585792B1 - Verfahren zur Rückführung eines gebrauchten photographischen Entwicklers und photographischer wiederverwendeter Entwickler - Google Patents

Verfahren zur Rückführung eines gebrauchten photographischen Entwicklers und photographischer wiederverwendeter Entwickler Download PDF

Info

Publication number
EP0585792B1
EP0585792B1 EP93113548A EP93113548A EP0585792B1 EP 0585792 B1 EP0585792 B1 EP 0585792B1 EP 93113548 A EP93113548 A EP 93113548A EP 93113548 A EP93113548 A EP 93113548A EP 0585792 B1 EP0585792 B1 EP 0585792B1
Authority
EP
European Patent Office
Prior art keywords
developer
recycled
bromide
spent
developing agent
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
EP93113548A
Other languages
English (en)
French (fr)
Other versions
EP0585792A3 (en
EP0585792A2 (de
Inventor
Rose Passarella
Daniel Frederick Juers
Paul Leonard Oertel, Jr.
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.)
Agfa Gevaert NV
Original Assignee
Agfa Gevaert NV
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 Agfa Gevaert NV filed Critical Agfa Gevaert NV
Publication of EP0585792A2 publication Critical patent/EP0585792A2/de
Publication of EP0585792A3 publication Critical patent/EP0585792A3/en
Application granted granted Critical
Publication of EP0585792B1 publication Critical patent/EP0585792B1/de
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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
    • G03C5/00—Photographic processes or agents therefor; Regeneration of such processing agents
    • G03C5/26—Processes using silver-salt-containing photosensitive materials or agents therefor
    • G03C5/29—Development processes or agents therefor
    • G03C5/31—Regeneration; Replenishers
    • 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
    • G03C5/00—Photographic processes or agents therefor; Regeneration of such processing agents
    • G03C5/26—Processes using silver-salt-containing photosensitive materials or agents therefor
    • G03C5/29—Development processes or agents therefor
    • G03C5/30—Developers

Definitions

  • the invention relates to a process of recycling spent photographic developer compositions wherein the spent developer is collected and reconstituted and can be re-used without detrimental effect on films processed therein.
  • Photographic developer compositions are well-known in the art.
  • the development of exposed silver halide photographic elements comprises a multiple step process of development, fixing, washing and optionally a stopping step.
  • the development step is conventionally undertaken with an aqueous alkaline developer composition containing a developer, also known as a developing agent either singly or with one or more additional developing agents.
  • a comprehensive list of developing agents is provided in C. E. K. Mees, The Theory of the Photographic Process, Chapters 14-15, The Macmillan Company (1959, Rev. Ed.)
  • the most commonly used developing agent, particularly for processing black-and-white photographic silver halide elements is hydroquinone.
  • the hydroquinone or other suitable developing agent serves as a strong silver reducing agent to reduce the silver halide grains containing a latent image to yield the developed photographic image.
  • Hydroquinone-based developer compositions typically contain relatively high levels of sulfite-based components. Also, the pH of hydroquinone-based developer compositions is maintained within strict alkaline ranges with alkaline buffers, such as carbonates, phosphates, borates, etc., either alone or in combination with hydroxides. While hydroquinone-based developer compositions have been successfully employed for many years, recently the use of these conventional developer compositions have been imposed with various guidelines and regulations due to the toxicity and environmental hazards associated with the hydroquinone, sulfite, and other components as well as the alkaline nature of the developer.
  • alkaline buffers such as carbonates, phosphates, borates, etc.
  • U.S. Patent 2,688,549 Another class of developing agents are disclosed in U.S. Patent 2,688,549, which teaches the use of ascorbic acid and sugar-type derivatives thereof as developing agents in photographic developers. Because ascorbic acid and its derivatives are not considered hazardous to the environment, it is desirable to have developer compositions which use these developing agents. Similarly, U.S. Patent 5,098,819 teaches improved photographic developer compositions which are free of hydroquinone and free of alkali metal hydroxides and which utilize ascorbic acid, derivatives and salts thereof as the developing agents.
  • developer compositions are highly alkaline with pH of at least 9.5, and they may also contain alkali sulfites as antioxidants in approximate amounts from 10% to 100% of the amount of the developing agent.
  • effluents from spent photographic developers have a Chemical Oxygen Demand (COD) of about 70,000 to 100,000 ppm, which exceeds the current limits set by the Environmental Protection Agency and other regulatory agencies.
  • the COD value represents the degree to which a solution will compete with biological systems for the supply of oxygen.
  • EP-A-0 498 968 discloses a photographic developing solution containing an ascorbic acid derivative; the document also discloses that the ascortic acid derivative could be recycled for a great part.
  • a major obstacle to recycling is being able to reconstitute the developer such that the performance of photographic materials in recycled developer is equivalent or substantially equivalent to the performance of the photographic materials in fresh developer.
  • Conventional hydroquinone-based developers are poor recycling prospects because the oxidation products of hydroquinone (formed during development of photographic materials) are developing agents themselves and thus contribute to the complexity of the developer composition. The development activity of these oxidation products makes it difficult, if not impossible, to reconstitute spent hydroquinone-type developer compositions to obtain a developer composition having acceptable performance.
  • the degradation (i.e., oxidation) of hydroquinone produces large, dark (almost black in color) polymeric compounds which are difficult to quantitatively analyze and separate. The presence of these degradation products in developer compositions contributes to sludge formation and staining of photographic elements processed therein.
  • the present invention is based upon the observation that ascorbic acid-type developing agents produce light-colored oxidation products and the discovery that these products do not affect the performance of the developer composition. It has also been discovered that the presence of these products does not produce undesirable effects (such a staining) to photographic elements processed therein.
  • the present invention comprises a recycled black-and-white photographic developer composition made according to the above process.
  • the hydroquinone-free black-and-white photographic developer composition comprises: Ingredients Amount (grams) sulfite ion 3 to 30 sequestering agent 1 to 7 bromide ion 1.5 to 10.0 developing agent 20 to 90 secondary developing agent 0.25 to 3.0 antifoggants 0.05 to 0.65 development accelerator 0.01 to 3.0 Water to make 1 Liter
  • Non-hydroquinone containing photographic developer compositions are disclosed, for example, in the aforementioned U.S. Patents and in U.S. Patent Application Serial Nos. 07/683,248, filed April 10, 1991 and 07/684,192, filed April 12, 1991. All of these references disclose the use of ascorbic acid-type developing agents, which are preferred in the present invention because they produce light-colored oxidation products which do not interfere with development, and thus, can be successfully reused to provide an environmentally sound method of developing photographic materials without detrimental effect on the performance of the photographic materials.
  • the developing agent must be one which avoids the combination of disadvantages presented by hydroquinone-type developing agents. In other words, it must be one which either (1) does not interfere with the developer activity or produce undesirable effects on photographic elements processed therein; or (2) is readily removed from the spent developer. Because of the complexity of developer compositions used to process color films, they are not considered to be viable candidates for recycling under the present process.
  • Developing agents which are employed in the present invention are selected from (1) ascorbic acid and sugar-type derivatives thereof; (2) stereoisomers and diastereoisomers of ascorbic acid, such as for example erythorbic acid, and their sugar-type derivatives; (3) salts and mixtures of (1) and (2); (4) 2-keto gluconic acid and derivatives thereof, and (5) mixtures of (1) through (4).
  • Example of such compounds include, DL-ascorbic acids, sorboascorbic acid, ⁇ -lactoascorbic acid, maltoascorbic acid, L-araboascorbic acid, sodium ascorbate, potassium ascorbate, sodium erythorbate and potassium erythorbate, 2-keto gluconates, potassium, sodium, ammonium, and methyl derivatives thereof.
  • Most preferred as the developing agents are ascorbic acid, sodium ascorbate, erythorbic acid, and sodium erythorbate.
  • the developer composition may contain a multitude of conventional adjuvants which serve various functions such as secondary developing agents, antifogging agents, buffers, sequestering agents, swelling control agents, and development accelerators.
  • adjuvants are well known to those of ordinary skill in the art.
  • Preferred secondary developing agents are pyrazolidone or metol and derivatives thereof, with 4-hydroxymethyl-4-methyl-1-phenyl-3-pyrazolidone and 1-phenyl-3-pyrazolidone being particularly preferred.
  • antifogging agents examples include benzotriazole, phenylmercaptotetrazole, and benzimidazole and derivatives thereof, used alone or in admixture.
  • Soluble bromides particularly alkali metal bromides (e.g., potassium bromide, sodium bromide) are the preferred restrainers. It is preferred to have both antifoggant agents and a restrainer in the developer. As discussed hereinbelow, it is particularly preferred for the developer to contain from 7 to 10 grams/Liter of an alkali metal bromide, whereby a greater percentage of spent developer can be recycled and reused in accordance with the present process.
  • sequestering agents or chelating agents
  • sequester trace metal ions e.g., copper and iron ions
  • Preferred sequestering agents are sodium salts of EDTA.
  • an antioxidant is also present in the developer composition.
  • Antioxidants are normally used in developer compositions as preservatives, however, such compounds serve the additional function of an accelerating compound in the preferred developer composition disclosed herein.
  • suitable antioxidants include alkali metal sulfites, bisulfites, metabisulfites and carbonyl-bisulfites adducts.
  • a preferred antioxidant is sodium bisulfite.
  • the pH of the developer is adjusted into the range of 9.0 to 11.0 by adding one or more of an alkali metal carbonate, such as sodium or potassium carbonate; an alkali metal bicarbonate, such as sodium or potassium bicarbonate; and, an alkali metal hydroxide.
  • an alkali metal carbonate such as sodium or potassium carbonate
  • an alkali metal bicarbonate such as sodium or potassium bicarbonate
  • an alkali metal hydroxide Preferred are potassium hydroxide and potassium carbonate in a ratio of 2 to 1.
  • a development accelerator may be included in the developer composition to increase developer activity to that of conventional development times.
  • a development accelerator in the ascorbic acid based developer compositions discussed above renders such compositions equivalent or substantially equivalent in development activity to conventional hydroquinone-based developers for all families of films common to graphic arts, i.e., camera, contact, and photoelectronic (e.g., scanner and imagesetting) films and papers.
  • Developer accelerators suitable for use in this invention include quaternary ammonium compounds and aryl hydrazides, such as those disclosed in U.S. 4,937,160.
  • the preferred development accelerators are the quaternary ammonium compounds disclosed by Pangratz in U.S. Serial Number 07/801,347.
  • a particularly preferred quaternary ammonium development accelerator is 1-phenethyl-2-picolinium bromide (PPB).
  • a suitable non-hydroquinone developer composition may comprise: Ingredients Amount (grams) sulfite 3 to 50 sequestering agent 1 to 7 bromide 1.5 to 10.0 developing agent 20 to 90 secondary developing agent 0.25 to 3.0 antifoggants 0.05 to 0.65 development accelerator 0.01 to 3.0 Water to make 1 Liter
  • a typical and preferred developer composition will comprise: Amount (grams) Ingredient Range Preferred Sulfite 10 - 30 15.8 Tri-sodium EDTA 2 - 7 3.5 Potassium bromide 7 - 10 8 Sodium Erythorbate 20 - 60 40 Glucono Delta Lactone 0.1 - 1.0 0.7 4-hydroxymethyl-4-methyl-1-phenyl-3-pyrazolidone 0.25 - 1 0.5 Benzotriazole 0.15 - 0.35 0.25 Phenylmercaptotetrazole 0.025 - 0.1 0.05 PPB 0 - 0.5 0.3 Water to make 1 Liter
  • the process of recycling spent photographic developer in accordance with the present invention comprises the steps of collecting the spent developer and reconstituting the spent developer for reuse as specified in claim 1.
  • the first step in the process is to collect spent developer.
  • spent developer as used herein, means a developer composition which has been used to process photographic film or which otherwise has lost some of its development activity as compared to fresh or virgin developer.
  • the collection step in the present process may conveniently be practiced by collecting developer purged from a developer tank of a processor (such as during processing and/or during automatic replenishment of the developer) in an off-line tank until a sufficient quantity of spent developer is available for the next step. It is to be understood that the process of the present invention does not require any particular amount of spent developer be collected before the reconstituting step. However, for obvious reasons, it is desirable for the present process to be practiced in batch quantities.
  • the collection step includes the separation of liquid developer from any particulate matter present therein. It is not uncommon for spent developer to contain a variety of foreign particulate matter, such as gelatin, conglomerates of silver, hair, dirt, and paper clips.
  • the separation of liquid developer from particulate matter may be practiced in any conventional manner, such as by decanting or filtration.
  • the next step in the present process comprises reconstituting the developer for reuse.
  • fresh developer denotes a developer which is newly mixed, and/or which has not been used to develop a significant amount of film, and/or which has not been held at elevated development temperatures, i.e., 35°C to 43,3°C (95°F to 110°F), for any extended period of time.
  • the reconstituting step may involve the addition of certain developer components to increase the concentration thereof or the dilution of the spent developer to decrease the concentration of components. More particularly, it is well known that many developer ingredients are wholly or partially consumed during development of photographic elements. Thus, the concentration of such ingredients in spent developer would be lower than the concentration in fresh developer. In the reconstituting step, these ingredients would be added to the spent developer.
  • both an addition and dilution will be necessary to reconstitute the spent developer.
  • the result of the reconstituting step should be a developer composition that is substantially the same as a fresh developer composition.
  • the reconstituted developer composition would also contain the oxidation products of the ascorbic acid-type developing agents.
  • the analysis step would comprise an analysis of the spent developer to determine the concentration of the various ingredients which are to be reconstituted and the pH.
  • Conventional analytical methods such as titration, spectroscopy and chromatography, may be used to conduct the analysis of the spent developer.
  • the spent developer should be analyzed for the concentration of developing agent (both primary and secondary) and antifoggant(s), since these components are usually critical to the performance of a developer.
  • the concentration of the bromide ion in the spent developer solution is generally dependent upon the mix of films processed in the developer, i.e., the proportion of the processed films which are totally or partially silver bromide grain films.
  • the spent developer may not need to be diluted to the extent that the spent developer would if some of the films processed contained silver bromide.
  • Another factor which may influence the concentration of bromide ion in the spent developer includes the amount of developed density, i.e., the proportion of the imaged film which is high density and low density.
  • a typical non-hydroquinone developer composition for black-and-white films will contain from 2 to 3 g/L of bromide ion, which can increase to 8 to 10 g/L in spent developer. Thus, in reconstituting such developers, it may be necessary to dilute the spent developer from 70% to 30% of the collected volume to reduce the bromide ion concentration to acceptable levels.
  • the recycled developer resulting from the present process would comprise between 30-70% spent developer and 70-30% fresh ingredients.
  • the pH of the developer should be adjusted using one or more of the well known adjuvants for that purpose.
  • the pH should be between 9.0 and 11.0.
  • composition of the recycled developer will not (and need not) be identical to the composition of fresh developer. Indeed, as noted previously, ascorbic acid-type developing agents degrade to light-colored oxidation products. The presence of these products does not interfere with the activity of the recycled developer and they do not adversely affect photographic elements processed therein. Therefore, these oxidation products need not be removed from the recycled developer. Similarly, ingredients such as carbonates and hydroxides, which serve only as pH adjusting and buffering agents, may be substituted with equivalent alkali buffering and adjusting agents in the reconstituting step, so long as the recycled developer has the proper pH and buffer capacity.
  • Photographic developers that have been recycled according to the present process can be used in the same manner as fresh developer solutions, including as a replenishment solution and to initially charge the processor. They may be used in a variety of processing equipment and techniques well known to those skilled in the art.
  • a fresh developer composition was made having the composition as shown in Table A.
  • Ingredient Grams/Liter working strength Tri-sodium ethylene-diaminotetraacetic acid (EDTA) 2 Sodium bisulfite 10 Potassium bromide 3 Erythorbic acid 80 4-hydroxymethyl-4-methyl-1-phenyl-3-pyrazolidone 0.5 Benzotriazole 0.5 Phenylmercaptotetrazole(PMT) 0.1 Water to 1 Liter
  • the pH of the solution was adjusted to 10.5 using a hydroxide and carbonate buffer solution, (approximately a 2:1 ratio hydroxide:carbonate).
  • the developer solution was placed into the developer tank of a deep tank processor and maintained at 37,8°C (100°F).
  • Spent developer developer which was purged from the development tank during processing of the films and/or during replenishment
  • the spent developer was filtered with a 10 ⁇ m particle size filter to remove particulate matter therefrom.
  • a sample of the spent developer was analyzed to determine the concentration of potassium bromide, erythorbic acid, Dimezone-S®, PMT, and benzotriazole.
  • the concentration of bromide ion was determined using titration.
  • the concentration of erythorbic acid was determined using UV spectroscopy.
  • the concentrations of PMT, Dimezone-S and benzotriazole were determined using high performance liquid chromatography (HPLC). Results of the analysis are shown in Table B.
  • Example 1 was repeated with the exception that bromide-free developer was used instead of water in the reconstitution step.
  • the amounts of developer ingredients and bromide-free developer are indicated in Table D. Sensitometric activity was as reported in Table C, above.
  • a fresh developer composition was made as shown in Table E.
  • Ingredient Gram/liter working strength Tri-sodium ethylene-diaminotetraacetic acid (EDTA) 3.5 Sodium bisulfite 22 Potassium bromide 8 Erythorbic acid 40 4-hydroxymethyl-4-methyl-1-phenyl-3-pyrazolidone 0.5 Benzotriazole 0.25 Phenylmercaptotetrazole(PMT) 0.05 Phenylethyl picolinium bromide (PPB) Water to 1 Liter 0.3
  • Example 1A The pH of the solution was adjusted to 10.7 using a 2:1 hydroxide:carbonate buffer solution.
  • the developer solution was placed into the developer tank of a deep tank processor and maintained at 37,8°C (100°F).
  • Various black-and-white graphic arts films were processed and sensitometrically tested, and spent developer collected as in Example 1A.

Landscapes

  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Silver Salt Photography Or Processing Solution Therefor (AREA)

Claims (12)

  1. Ein Verfahren zur Rückführung von hydrochinonfreien fotografischen Schwarzweiß-Entwicklerzusammensetzungen, das die folgenden Stufen umfaßt :
    (a) das Sammeln von verbrauchtem Entwickler, wobei die Entwicklerzusammensetzung eine Entwicklersubstanz aus der folgenden Gruppe enthält :
    (1) Ascorbinsäure und Ascorbinsäure-Zuckerderivate,
    (2) Stereoisomere und Diastereoisomere von Ascorbinsäure und Ascorbinsäure-Zuckerderivate,
    (3) Salze und Mischungen aus (1) und (2),
    (4) 2-Ketogluconsäure und deren Derivate, und
    (5) Mischungen aus (1) bis (4), und
    (b) die Rekonstituierung des verbrauchten Entwicklers zwecks seiner Wiederverwertung, wobei zur Rekonstituierung (1) der verbrauchte Entwickler filtriert und/oder (2) der verbrauchte Entwickler analysiert wird, und anschließend (3) frische Ingredienzien zum Entwickler gegeben werden und (4) der Entwickler verdünnt wird.
  2. Verfahren nach Anspruch 1, dadurch gekennzeichnet, daß die frischen Ingredienzien Entwicklersubstanz, Hilfsentwickler-substanz und Schleierschutzmittel umfassen.
  3. Verfahren nach Anspruch 2, dadurch gekennzeichnet, daß das Schleierschutzmittel Benztriazol, Phenylmercaptotetrazol, Benzimidazol oder ein Derivat derselben ist.
  4. Verfahren nach Anspruch 2, dadurch gekennzeichnet, daß die Hilfsentwicklersubstanz Pyrazolidon, Metol oder ein Derivat derselben ist.
  5. Verfahren nach Anspruch 1, dadurch gekennzeichnet, daß die fotografische Entwicklerzusammensetzung zwischen 7 und 10 g/l eines Alkalimetallbromids enthält.
  6. Verfahren nach Anspruch 1, dadurch gekennzeichnet, daß die fotografische Entwicklerzusammensetzung folgende Ingredienzien enthält : Ingrediens Menge (g) Sulfit 3 bis 50 Komplexbildner 1 bis 7 Bromid 1,5 bis 10,0 Entwicklersubstanz 20 bis 90 Hilfsentwickler 0,25 bis 3,0 Antischleiermittel 0,05 bis 0,65 Entwicklungsbeschleuniger 0,01 bis 3,0 Wasser zum Auffüllen auf 1 Liter
  7. Verfahren nach Anspruch 1, dadurch gekennzeichnet, daß die fotografische Entwicklerzusammensetzung folgende Ingredienzien enthält : Ingrediens Menge (g) Sulfition 15,8 Trinatriumethylendiamin-tetraessigsäure 3,5 Kaliumbromid 8 Natriumerythroascorbat 40 Glucono-δ-lacton 0,7 4-Hydroxymethyl-4-methyl-1-phenyl-3-pyrazolidon 0,5 Benztriazol 0,25 Phenylmercaptotetrazol 0,05 Phenylethylpicoliniumbromid 0,3 Wasser zum Auffüllen auf 1 Liter
  8. Eine wiederverwertbar gemachte fotografische Schwarzweiß-Entwicklerzusammensetzung, die nach dem in Anspruch 1 beschriebenen Verfahren hergestellt ist.
  9. Die wiederverwertbar gemachte Entwicklerzusammensetzung von Anspruch 8, die wenigstens 30% (Volumen-%) wiederverwertbar gemachtes Material enthält.
  10. Die wiederverwertbar gemachte Entwicklerzusammensetzung von Anspruch 9, die wenigstens 7 bis 10 g/l eines Alkalimetallbromids enthält.
  11. Die wiederverwertbar gemachte fotografische Entwicklerzusammensetzung von Anspruch 8, die folgende Ingredienzien enthält : Ingrediens Menge (g) Sulfit 3 bis 50 Komplexbildner 1 bis 7 Bromid 1,5 bis 10,0 Entwicklersubstanz 20 bis 90 Hilfsentwickler 0,25 bis 3,0 Antischleiermittel 0,05 bis 0,65 Entwicklungsbeschleuniger 0,01 bis 3,0 Wasser zum Auffüllen auf 1 Liter
  12. Die wiederverwertbar gemachte fotografische Entwicklerzusammensetzung von Anspruch 8, die folgende Ingredienzien enthält : Ingrediens Menge (g) Sulfition 15,8 Trinatriumethylendiamintetraessigsäure 3,5 Kaliumbromid 8 Natriumerythroascorbat 40 Glucono-δ-lacton 0,7 4-Hydroxymethyl-4-methyl-1-phenyl-3-pyrazolidon 0,5 Benztriazol 0,25 Phenylmercaptotetrazol 0,05 Phenylethylpicoliniumbromid 0,3 Wasser zum Auffüllen auf 1 Liter
EP93113548A 1992-09-04 1993-08-25 Verfahren zur Rückführung eines gebrauchten photographischen Entwicklers und photographischer wiederverwendeter Entwickler Expired - Lifetime EP0585792B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US94134392A 1992-09-04 1992-09-04
US941343 1992-09-04

Publications (3)

Publication Number Publication Date
EP0585792A2 EP0585792A2 (de) 1994-03-09
EP0585792A3 EP0585792A3 (en) 1994-08-10
EP0585792B1 true EP0585792B1 (de) 1999-11-24

Family

ID=25476315

Family Applications (1)

Application Number Title Priority Date Filing Date
EP93113548A Expired - Lifetime EP0585792B1 (de) 1992-09-04 1993-08-25 Verfahren zur Rückführung eines gebrauchten photographischen Entwicklers und photographischer wiederverwendeter Entwickler

Country Status (5)

Country Link
EP (1) EP0585792B1 (de)
JP (1) JPH06161057A (de)
AU (1) AU666213B2 (de)
CA (1) CA2105532A1 (de)
DE (1) DE69327079T2 (de)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3078431B2 (ja) * 1993-09-27 2000-08-21 富士写真フイルム株式会社 黒白ハロゲン化銀写真感光材料の現像方法
US5798204A (en) * 1994-07-26 1998-08-25 Fuji Photo Film Co., Ltd. Development processing method of ultrahigh-contrast black-and-white silver halide photographic material
DE69515939T2 (de) * 1994-08-11 2000-07-20 Konishiroku Photo Ind Verfahren zur Verarbeitung eines photographischen lichtempfindlichen Silberhalogenidmaterials
US5648205A (en) * 1994-10-13 1997-07-15 Fuji Photo Film Co., Ltd. Processing method for silver halide photographic material
EP0731381B1 (de) * 1995-02-21 1999-12-08 Agfa-Gevaert N.V. Entwicklerlösung und Verfahren zum Entwickeln eines belichteten, photographischen Silberhalogenidmaterials
EP0752618A3 (de) * 1995-06-12 1997-01-22 E.I. Du Pont De Nemours And Company Hydrochinon-Entwickler, Verfahren zur Wiederaufbereitung verbrauchter Hydrochinon-Entwickler und ein wiederaufbereiteter Entwickler
US5702875A (en) * 1996-06-28 1997-12-30 Eastman Kodak Company Weakly alkaline ascorbic acid developing composition, processing kit and method using same
US5866309A (en) * 1997-10-22 1999-02-02 Fitterman; Alan S. Method for processing roomlight handleable photographic elements
US5932398A (en) * 1997-11-14 1999-08-03 Eastman Kodak Company Kit for roomlight processing of black-and-white photographic elements
US5871890A (en) * 1997-11-14 1999-02-16 Eastman Kodak Company Method for processing roomlight handleable radiographic films using two-stage development
FR2776774B1 (fr) * 1998-03-24 2000-05-26 Eastman Kodak Co Procede et dispositif pour le traitement des produits photographiques aux halogenures d'argent
US6242143B1 (en) 1998-03-24 2001-06-05 Eastman Kodak Company Method and device for the processing of silver halide photographic materials
FR2778461B1 (fr) * 1998-05-05 2000-06-30 Eastman Kodak Co Procede et dispositif pour le controle du traitement chromogene des produits photographiques aux halogenures d'argent
JP3576052B2 (ja) * 1999-10-29 2004-10-13 ユニ・チャーム株式会社 使い捨て着用物品に使用する可撓性複合シート
JP4865664B2 (ja) 2007-09-28 2012-02-01 富士フイルム株式会社 多孔性担体内で２以上の液を混合する方法
EP2065706B1 (de) 2007-11-29 2012-11-07 FUJIFILM Corporation Immunochromatografieverfahren
CN102362222A (zh) 2009-03-27 2012-02-22 卡尔斯特里姆保健公司 引入显影剂的射线照射卤化银膜

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0530889A1 (de) * 1991-08-21 1993-03-10 Kodak Limited Methode zur Auffüllung von photographischen Entwicklerlösungen
EP0573700A1 (de) * 1992-06-09 1993-12-15 Agfa-Gevaert N.V. Regenierung eines Ascorbinsäure- und 3-Pyrazolidinonderivate enthaltenden Entwicklers

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5051731A (de) * 1973-08-24 1975-05-08
JPS60196753A (ja) * 1984-03-19 1985-10-05 Fuji Photo Film Co Ltd 現像方法
FR2578486B1 (fr) * 1985-03-08 1987-06-12 Bertin & Cie Procede et dispositif de positionnement d'objets les uns par rapport aux autres, en particulier des rouleaux d'impression de couleurs dans une presse rotative offset
DE3737325A1 (de) * 1987-10-30 1989-05-11 Guetling Gmbh Verfahren und vorrichtung zum wiederaufbereiten von fixierbaedern
GB8902186D0 (en) * 1989-02-01 1989-03-22 Kodak Ltd Photographic processing
JPH03174154A (ja) * 1989-09-07 1991-07-29 Fuji Photo Film Co Ltd ハロゲン化銀カラー写真感光材料の処理方法
US5278035A (en) * 1990-01-31 1994-01-11 Knapp Audenried W Non-toxic photographic developer composition for processing x-ray films in automatic film processors
JP2704668B2 (ja) * 1990-04-13 1998-01-26 富士写真フイルム株式会社 カラー印画紙の処理方法
EP0498968B1 (de) * 1991-02-14 1996-05-22 Agfa-Gevaert N.V. Photographisches Entwicklungsverfahren, in dem ein Ascorbin-Säure-Derivat eingesetzt wird
EP0569580A1 (de) * 1991-12-02 1993-11-18 E.I. Du Pont De Nemours And Company Verbesserte entwicklersysteme für hydrazin enthaltende filme

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0530889A1 (de) * 1991-08-21 1993-03-10 Kodak Limited Methode zur Auffüllung von photographischen Entwicklerlösungen
EP0573700A1 (de) * 1992-06-09 1993-12-15 Agfa-Gevaert N.V. Regenierung eines Ascorbinsäure- und 3-Pyrazolidinonderivate enthaltenden Entwicklers

Also Published As

Publication number Publication date
AU666213B2 (en) 1996-02-01
EP0585792A3 (en) 1994-08-10
DE69327079T2 (de) 2000-09-07
EP0585792A2 (de) 1994-03-09
DE69327079D1 (de) 1999-12-30
AU4607893A (en) 1994-03-10
JPH06161057A (ja) 1994-06-07
CA2105532A1 (en) 1994-03-05

Similar Documents

Publication Publication Date Title
EP0585792B1 (de) Verfahren zur Rückführung eines gebrauchten photographischen Entwicklers und photographischer wiederverwendeter Entwickler
EP0603586A1 (de) Photographische Entwicklerlösung
EP0589624B1 (de) Feststoffzusammensetzung zur farbphotographischen Entwicklung für farbphotographisches lichtempfindliches Silberhalogenidmaterial
DE69205661T2 (de) Photographisches Behandlungsmittel.
EP0456725B1 (de) Bleichfixier-regenerationssatz und verwendung davon in photographischer behandlung
US5707790A (en) Developing composition for silver halide photographic light-sensitive material
US5210010A (en) Silver halide developing solutions
EP0661593B1 (de) Fixierzusatzstoffe zur Verwendung mit Bleichmittel die Eisen-Komplex enthalten zur Verbesserung der Entsilberung
US5554491A (en) Use of an alkaline prebath to activate an acidic peroxide bleach solution for processing color photographic elements
EP0611986A1 (de) Feststoffzusammensetzung zur photographischen Verarbeitung eines farbphotographischen lichtempfindlichen Silberhalogenidmaterials
JPH025048A (ja) カラー写真現像液及びカラー写真材料の現像方法
US5670304A (en) Recycling spent hydroquinone developer and a recycled hydroquinone developer
EP0696759B1 (de) Verfahren zur Verarbeitung eines photographischen lichtempfindlichen Silberhalogenidmaterials
EP0594053A2 (de) Fixierbäder
JPH10288829A (ja) ハロゲン化銀写真感光材料用処理剤の再生方法
JP2931688B2 (ja) 写真用処理剤組成物
JPH0462545A (ja) 写真用処理剤組成物
EP0803082B1 (de) Verarbeitung monochromer photographischer silberhalogenidmaterialien
EP0733945B1 (de) Entwicklerzusammensetzung mit verbesserter Stabilität gegen Luft für ein belichtetes, photographisches Produkt
Roosen et al. The use of bleach-fixing baths in color motion-picture film processing
EP0512311B1 (de) Entwicklungslösung für Verfahren mit geringem Chemieüberlauf
EP0742481A1 (de) Verfahren zur Verarbeitung photographischer Schwarzweissmaterialien
JP2709845B2 (ja) 節水効率に優れた自動現像装置及び該装置を用いた排水処理方法
EP0601415A1 (de) Photographische Entwicklerlösung
EP0772085A2 (de) Bleich-Auffrischerzusammensetzung und deren Verwendung zur Behandlung von farbfotografischen Umkehrelementen

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: A2

Designated state(s): BE DE FR GB IT

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

AK Designated contracting states

Kind code of ref document: A3

Designated state(s): BE DE FR GB IT

17P Request for examination filed

Effective date: 19941220

17Q First examination report despatched

Effective date: 19971124

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: AGFA-GEVAERT N.V.

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

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): BE DE FR GB IT

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRE;WARNING: LAPSES OF ITALIAN PATENTS WITH EFFECTIVE DATE BEFORE 2007 MAY HAVE OCCURRED AT ANY TIME BEFORE 2007. THE CORRECT EFFECTIVE DATE MAY BE DIFFERENT FROM THE ONE RECORDED.SCRIBED TIME-LIMIT

Effective date: 19991124

Ref country code: FR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 19991124

Ref country code: BE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 19991124

REF Corresponds to:

Ref document number: 69327079

Country of ref document: DE

Date of ref document: 19991230

EN Fr: translation not filed
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: 20000831

REG Reference to a national code

Ref country code: GB

Ref legal event code: 746

Effective date: 20000821

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
REG Reference to a national code

Ref country code: GB

Ref legal event code: IF02

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20020625

Year of fee payment: 10

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20030620

Year of fee payment: 11

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: 20040825

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20040825