US3615496A - Photographic developer compositions - Google Patents

Photographic developer compositions Download PDF

Info

Publication number
US3615496A
US3615496A US702205A US3615496DA US3615496A US 3615496 A US3615496 A US 3615496A US 702205 A US702205 A US 702205A US 3615496D A US3615496D A US 3615496DA US 3615496 A US3615496 A US 3615496A
Authority
US
United States
Prior art keywords
benzyl alcohol
dispersion
developer
water
photographic
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
US702205A
Other languages
English (en)
Inventor
Roy Jones Kanous
Henry Josef Fassbender
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.)
Eastman Kodak Co
Original Assignee
Eastman Kodak Co
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 Eastman Kodak Co filed Critical Eastman Kodak Co
Application granted granted Critical
Publication of US3615496A publication Critical patent/US3615496A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

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
    • G03C5/264Supplying of photographic processing chemicals; Preparation or packaging thereof
    • G03C5/266Supplying of photographic processing chemicals; Preparation or packaging thereof of solutions or concentrates

Definitions

  • This invention relates to photographic processing solutions.
  • this invention relates to photographic color developers and processes used in the production thereof, especially wherein the color developer components are prepackaged in solution form for ready mixing and use by the trade.
  • the developers In the processing of photographic film and paper, wide varieties and large quantities of photographic developers are utilized. To facilitate the preparation and use of these developers, it has been found desirable to package the developers in liquid form usually as concentrates. However, some of the individual components of these developers, especially of color developers, react with one another and at the concentrations desired are not miscible. For these reasons the individual components have been conveniently packaged in separate compartments of a single package. In the separate compartments, the essential ingredients are desirably either liquid per se or in solution so that mixing the ingredients into a complete developer involves little time-consuming dissolution.
  • the separate compartments have, for example, respectively contained benzyl alcohol, base plus buffering ingredients, hydroxylamine sulfate and an acidic solution of developing agent pulse sulfite.
  • compositions and methods which not only obviate the necessity of packaging benzyl alcohol separately from the other ingredients in liquid photographic processing concentrates, but also facilitate the dissolution of benzyl alcohol to form the ready-to-use processing solution, without detracting from the effectiveness of the overall processing characteristics of the solution.
  • stable, concentrated dispersions, of benzyl alcohol in water are formed if the concentrated composition contains water-soluble polymeric carbohydrates or polymeric amides, especially cellulose-based emulsifying agents.
  • the extremely stable dispersions of benzyl alcohol pulse emulsifying agents in water are formed if the composition further contains ionic materials, for example, salts such as alkali metal sulfates, sulfites, phosphates, borates, citrates, etc. or other substances which are necessary or desirable in the intended processing solution, such as hydroxylamine sulfate, etc.
  • ionic materials for example, salts such as alkali metal sulfates, sulfites, phosphates, borates, citrates, etc. or other substances which are necessary or desirable in the intended processing solution, such as hydroxylamine sulfate, etc.
  • salts such as alkali metal sulfates, sulfites, phosphates, borates, citrates, etc. or other substances which are necessary or desirable in the intended processing solution, such as hydroxylamine sulfate, etc.
  • a disper sion containing containing a water/cellulose-based emulsifying agent weight ratio of about l/.00l to 0.01, a water/benzyl alcohol weight ratio of about H to 25/ l and a water/salt ratio of l/.000l-0.33 presents a dispersion of outstanding stability.
  • the benzyl alcohol may thus be incorporated into a compartment of the processing solution containing an aqueous solution of other processing, e.g., developer, components and can be packaged in plastic, e.g., polyethylene containers.
  • the shipping, handling, and packaging costs for such processing compositions, therefore, can be substantially decreased.
  • compositions containing water, benzyl alcohol, and the indicated emulsifying agents can also readily be diluted with more water and/or solutions containing other precessing components with no appreciable oiling out" of the benzyl alcohol and if found to substantially diminish the mixing time normally involved in combining separated components of liquid processing concentrates, especially in forming color developers.
  • a water/emulsifying agent weight ratio of about 1/0.0020.0 l it is further desirable to maintain a water/benzyl alcohol weight ratio of about 1.] to 25/ l in the dispersion.
  • salts especially hydroxylamine sulfate, are also present such that the salt/water ratio is about 0.01-33/100, but limited generally only by the solubility of the selected salt in aqueous solution.
  • Such compositions are found to be resistant to separation as well as nonfoaming and have no appreciable detrimental effect when used in the desired photographic processing solution, e.g., color developers.
  • the minimum amount of cellulose-based emulsifier necessary may vary somewhat depending, inter alia, upon the particular emulsification agent( s) selected, the amount of water present and the amount and type of other components present, but there is desirably sufficient emulsifying agent to maintain a stable suspension of benzyl alcohol in the concentrate.
  • the stable dispersions described herein are those that are practically stable, i.e., dispersions which do not separate at all and those which do separate into apparently two or more layers on long standing but which readily redisperse upon a mere inversion of the container or at most with moderate agitation.
  • Water-soluble polymeric carbohydrate emulsifying agents and water-soluble polymeric amide emulsifying agents and water-soluble carbohydrate and polyamide derivatives are the only compositions found which form stable dispersions of benzyl alcohol in water.
  • Carbohydrate compositions which are effective are starch derivatives such as Ceron (Hercules Chemical Company), etc., Guar gums, for example, carboxymethyl Guar, etc., and water-soluble cellulose-based emulsifying agents such as cellulose sulfates, cellulose acetate sulfates, low acetyl containing cellulose acetates, sodium algenate, sodium hydroxypropyl algenate, methyl cellulose ethyl cellulose phthalates, mixed ethers of cellulose, e.g., isopropylmethyl ethers, etc., and hydroxyethyl cellulose compositions which result in dispersions of surprisingly outstanding effectiveness.
  • Polymeric amides of high effectiveness are the proteins,
  • the silver halide developing agents especially useful in the developer compositions of the present invention are the pphenylenediamine color-developing agents well known in the art especially those forming nondiffusing dyes with phenolic and reactive methylene couplers.
  • These developing agents include p-phenylenediamine and N,N-dialkyl-p-phenylenediamines wherein the alkyl groups or the aromatic nucleus may be substituted, for example: N,N-diethyl-p-phenylenediamine monohydrochloride, 2-amino-5- diethylaminotoluene monohydrochloride, 4-amino-N-ethyl- N-[fl-methanesulfonamidoethyU-m-toluidine sesquisulfate monohydrate, 4-amino-3-methyl-N-ethyl-N-[B-hydroxyethyll-aniline sulfate, 4-amino-3-(fl-methyl
  • the solution containing the developing agent be acidic to assist in the stabilization of the developing agent and also to keep the developing agent in solution.
  • the pH is preferably less than about 4.However, the optimum pH will vary depending upon the particular developing agent in use, for example, when 4- amino-N,N-diethyl-3-( N -methyl-B-rnethylsulfonamidoethyl aniline hydrochloride is used, it is desirable that the solution have a pH less than 1 particularly to keep the developing agent in solution in a concentrate.
  • sulfite may be present in accordance with the disclosure of U.S. Pat. Ser. No. 676,623 filed Oct. 19, 1967, by Kanous and Bimmler and other substances useful in the color development reaction may be present, such as antifoggants, e.g., benzotriazole, development restrainers, e.g., bromide and auxiliary black and white developing agents, such as the 3- pyrazolidone silver halide developing agents, e.g., 4,4- dimethyl-l-phcnyl-S-pyrazolidone.
  • antifoggants e.g., benzotriazole
  • development restrainers e.g., bromide
  • auxiliary black and white developing agents such as the 3- pyrazolidone silver halide developing agents, e.g., 4,4- dimethyl-l-phcnyl-S-pyrazolidone.
  • the sulfite and developing agents are usually desirable as a simple aqueous solution with or without added acid.
  • the combined concentration of the sulfite and developing agent can vary widely. Since the developer package is designed for shipment and storage, it is usually desirable to utilize the highest concentration of ingredients which will readily stay in acidic solution. More dilute solutions can, of course, be utilized depending upon the individual circumstances.
  • Packaging the benzyl alcohol in aqueous solutions of specific emulsifying agents generally is advantageous in packaging any compositions which require or desirably contain compounds such as benzyl alcohol, ultimately dispersed or dissolved in aqueous solution.
  • Such packaging is significant in photographic silver halide developer packages especially those which are to be utilized with well-known color products having differently sensitized silver halide emulsion layers containing nondiffusing coupler compounds, for example, those having superposed on a support, blue-, green-, and red-sensitized emulsion layers containing yellow, magenta, and cyan dye-forming couplers, respectively.
  • the developer compositions when mixed and ready for use can and desirably do contain the usual amounts of developing agent, sulfite and alkali as disclosed generally in the .lelley et al. U.S. Pat. No. 2,322,027.
  • packaged developer components advantageously are separated to the extent that in compartments containing developing agents, the sulfite concentration and the pH is controlled as indicated in U.S. Pat. Ser. No. 676,623, mentioned above with the benzyl alcohol dispersion included in one or more of the compartments.
  • Other components which may form part of the mixed developer package for example, additional sulfite, accelerators, complexing agents, buffers, e.g.,
  • citric acid-citrate, boric acid-borate, etc. are advantageously contained in the compartment conta ning the alkali, e.g., potassium hydroxide, although placing selected addenda in other or separate compartments may be desirable depending upon the particular ingredient chosen.
  • alkali e.g., potassium hydroxide
  • the packaged developer effectively may be a single package, for example, an outside container or cardboard box in which the developer components are compartmentalized.
  • the compartments can be an integral part of the exterior packaging material but advantageously are, at least in part, merely bottles of, for example, glass and/or plastic enclosed in the outside container.
  • the choice of sizes and shapes of the bottles which form the compartments can vary with the selected ingredients, concentrations desired, etc. Usually it is desirable to choose the bottle size, shape, etc. which will result in a total package of minimum size and weight to minimize shipping and storage costs. As a result, it may in some instances be desirable to place a single component type in a plurality of compartments, e.g., to conserve space.
  • Natrosol 250 H (a high-viscosity hydroxyethyl cellulose marketed by Hercules Chemical Company) is added to 20 ml. of water. The mixture is stirred for about 1 hour. To this solution l2.6 ml. of benzyl alcohol is added with stirring. After the addition is complete the mixture is vigorously stirred. The resulting dispersion appears stable at room temperature.
  • EXAMPLE 2 The dispersion of example 1 is utilized as component A of a four'component liquid color developer. The remaining components containing:
  • the solution appears completely homogeneous after only about one-half the time required for the dissolution of a similar developer devoid of hydroxyethyl cellulose.
  • the solution functions effectively and consistently as a color developer for color print material having respectively superposed on a paper support, blue-, green-, and red-sensitized emulsion layers containing yellow, magenta, and cyan dye-forming couplers, respectively, which has been exposed to a test pattern.
  • hydroxylamine sulfate 2.1 g. of hydroxylamine sulfate is dissolved in 10 ml. of water. To another 10 ml. of water is added 50 mg. of hydroxyethyl cellulose (Natrosol 250 H). After a period of soaking and stirring for about 1 hour the hydroxyethyl cellulose completely dissolves in the water. The two solutions are mixed together and 12.6 ml. of benzyl alcohol is added with stirring. The mixture is then vigorously shaken.
  • the dispersion thus formed is stable for over 2 months at 120 F.
  • hydroxylamine sulfate 2.l gms. of hydroxylamine sulfate is dissolved in 20 ml. of water. To this solution is added 50 mg. of hydroxyether cellulose (Natrosol 250 H). After soaking and stirring for about 1 hour the hydroxyethyl cellulose dissolves in the salt solution. To this solution benzyl alcohol is added with rapid stirring.
  • the developer functions effectively and consistently when utilized with photographic color print material as described above.
  • the dispersion is stable except that after a period the dispersion appears to separate into two layers. It is found that the dispersion is still stable but that the dispersed complexes of benzyl alcohol and emulsifying agent merely tend to be buoyant. Upon merely turning the container over, the dispersion appears homogeneous.
  • the dispersion functions effectively and is readily miscible with the photographic color developer components B and C listed in example 5.
  • EXAMPLE 9 A benzyl alcohol dispersion was prepared in the manner indicated in example 3 except that Natrosol l H is utilized in place of Natrosol 250 H. Comparable results are obtained both as to the dispersion itself and its effectiveness in a developer.
  • EXAMPLE 10 A benzyl alcohol dispersion is prepared in the manner indicated in example 3 except that the moderately low-viscosity hydroxyethyl cellulose (Natrosol 250 G) is utilize in placed of the higher viscosity analog. Comparable results are obtained both as to the dispersion itself and its effectiveness and ease of mixing with a photographic color developer.
  • the moderately low-viscosity hydroxyethyl cellulose Niatrosol 250 G
  • EXAMPLE 1 l A benzyl alcohol dispersion is prepared according to the procedure outlined in example 3 except that carboxyethyl Guar is utilized in place of the Natrosol. The dispersion appears stable for periods in excess of 1 week and functions well in photographic developers.
  • Example 12 A benzyl alcohol dispersion is prepared according to the procedure outlined in example 3 except that gelatin is utilized in place of the Natrosol. The dispersion appears stable for periods in excess of 1 week and functions well in photographic developers.
  • EXAMPLE 13 A benzyl alcohol dispersion is prepared according to the procedure outlined in example 3 except that carboxymethyl cellulose is utilized in place of the Natrosol. The dispersion appears stable for periods in excess of 1 week and functions well in photographic developers.
  • EXAMPLE [4 A benzyl alcohol dispersion is prepared according to the procedure outlined in example 3 except that carboxymethyl hydroxyethyl cellulose is utilized in place of the Natrosol. The dispersion appears stable for periods in excess of 1 week and functions well in photographic developers.
  • a unitary packaged developer kit in which at least some of the developer components are in separate compartments, said kit comprising at least one compartment containing a composition comprising water, benzyl alcohol, and an emulsifying agent selected from the group consisting the water-soluble polymeric carbohydrate emulsifying agents and watersoluble polymeric amide emulsifying agents and another compartment containing aqueous alkali and yet another compartment containing a p-phenylenediamine developing agent.
  • Tile developer kit of claim 1 wherein the emulsifying agent is hydroxyethyl cellulose and hydroxylamine sulfate is also present in said first-mentioned compartment.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Silver Salt Photography Or Processing Solution Therefor (AREA)
  • Polymerisation Methods In General (AREA)
US702205A 1968-02-01 1968-02-01 Photographic developer compositions Expired - Lifetime US3615496A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US70220568A 1968-02-01 1968-02-01
US74391768A 1968-07-11 1968-07-11

Publications (1)

Publication Number Publication Date
US3615496A true US3615496A (en) 1971-10-26

Family

ID=27106933

Family Applications (2)

Application Number Title Priority Date Filing Date
US702205A Expired - Lifetime US3615496A (en) 1968-02-01 1968-02-01 Photographic developer compositions
US743917A Expired - Lifetime US3615497A (en) 1968-02-01 1968-07-11 Benzyl alcohol dispersions

Family Applications After (1)

Application Number Title Priority Date Filing Date
US743917A Expired - Lifetime US3615497A (en) 1968-02-01 1968-07-11 Benzyl alcohol dispersions

Country Status (8)

Country Link
US (2) US3615496A (pt)
BE (1) BE727705A (pt)
CH (1) CH492237A (pt)
DE (1) DE1904917A1 (pt)
FR (1) FR2001119A1 (pt)
GB (1) GB1254726A (pt)
NL (1) NL6901642A (pt)
ZA (1) ZA6900393B (pt)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0087370A2 (en) * 1982-02-24 1983-08-31 EASTMAN KODAK COMPANY (a New Jersey corporation) Method for preparation of photographic color developing solutions
US4770979A (en) * 1981-12-24 1988-09-13 Konishiroku Photo Industry Co., Ltd. Developer composition
US6733960B2 (en) * 2001-02-09 2004-05-11 Eastman Kodak Company Digital film processing solutions and method of digital film processing

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5021250B2 (pt) * 1971-08-20 1975-07-22
DE3521713A1 (de) * 1985-06-18 1986-12-18 Henkel KGaA, 4000 Düsseldorf Oel-in-wasser-emulsionen mit verbessertem viskositaetsverhalten

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4770979A (en) * 1981-12-24 1988-09-13 Konishiroku Photo Industry Co., Ltd. Developer composition
EP0087370A2 (en) * 1982-02-24 1983-08-31 EASTMAN KODAK COMPANY (a New Jersey corporation) Method for preparation of photographic color developing solutions
US4414307A (en) * 1982-02-24 1983-11-08 Eastman Kodak Company Method and composition for preparation of photographic color developing solutions
EP0087370A3 (en) * 1982-02-24 1984-02-01 Eastman Kodak Company Method for preparation of photographic color developing solutions
US6733960B2 (en) * 2001-02-09 2004-05-11 Eastman Kodak Company Digital film processing solutions and method of digital film processing

Also Published As

Publication number Publication date
US3615497A (en) 1971-10-26
DE1904917A1 (de) 1970-02-19
CH492237A (fr) 1970-06-15
FR2001119A1 (pt) 1969-09-26
NL6901642A (pt) 1969-08-05
BE727705A (pt) 1969-07-01
ZA6900393B (pt)
GB1254726A (en) 1971-11-24

Similar Documents

Publication Publication Date Title
US6228567B1 (en) Homogeneous photographic color developing concentrate
US6017687A (en) Low replenishment color development using chloride ion-free color developer concentrate
US3574619A (en) Concentrated liquid color developers containing benzyl alcohol
US6428946B2 (en) Multi-part photographic color developing composition and methods of manufacture and use
US4987060A (en) Concentrated photographic developer composition and method of making it
US3615496A (en) Photographic developer compositions
US6159670A (en) Calcium ion stable photographic color developing concentrate and method of manufacture
US4414307A (en) Method and composition for preparation of photographic color developing solutions
US3814606A (en) Color photographic processing composition
US3721563A (en) Photographic developer concentrate
US3615572A (en) Acidic solution of phenylenediamine color developer and sulfite
JP2001142185A (ja) 写真用発色現像組成物
US4501812A (en) Photographic color developer composition packaged in two or more concentrated parts, particularly solutions, and concentrated color developer water solution
USRE28185E (en) Acidic solution of phenylenediamine
US6770429B2 (en) Single part color photographic developer concentrate
US6518003B1 (en) Three-part concentrated photographic color developing kit and methods of use
US6573035B1 (en) Stable multi-part photographic color developing composition and method of use
US2772973A (en) Stabilized color developers
JPS6355547A (ja) ハロゲン化銀カラー写真感光材料用発色現像液及びハロゲン化銀カラー写真感光材料の処理方法
US6599688B1 (en) Stable photographic color developing composition and method of use
US20060093970A1 (en) Combinations of preservatives and sequestrants to avoid formation of isonitrile malodor
MXPA99007381A (en) Concentrate developer of homogeneo photographic color of a single part and my manufacturing method