US3785824A - Photographic aqueous dispersion concentrates - Google Patents
Photographic aqueous dispersion concentrates Download PDFInfo
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- US3785824A US3785824A US00183703A US3785824DA US3785824A US 3785824 A US3785824 A US 3785824A US 00183703 A US00183703 A US 00183703A US 3785824D A US3785824D A US 3785824DA US 3785824 A US3785824 A US 3785824A
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- water
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- solvent
- dispersing agent
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- 239000006185 dispersion Substances 0.000 title claims abstract description 45
- 239000012141 concentrate Substances 0.000 title description 15
- 239000002904 solvent Substances 0.000 claims abstract description 44
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 41
- 239000002270 dispersing agent Substances 0.000 claims abstract description 30
- -1 silver halide Chemical class 0.000 claims abstract description 23
- 229920001577 copolymer Polymers 0.000 claims description 18
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical group OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 claims description 15
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 14
- 229920000642 polymer Polymers 0.000 claims description 14
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 12
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 11
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 10
- 150000002170 ethers Chemical class 0.000 claims description 10
- 229920000151 polyglycol Polymers 0.000 claims description 10
- 239000010695 polyglycol Substances 0.000 claims description 10
- 125000003118 aryl group Chemical group 0.000 claims description 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 5
- 239000005977 Ethylene Substances 0.000 claims description 5
- 235000019445 benzyl alcohol Nutrition 0.000 claims description 5
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 claims description 4
- 125000000129 anionic group Chemical group 0.000 claims description 3
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical group OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 claims description 2
- 229960005323 phenoxyethanol Drugs 0.000 claims description 2
- 238000000034 method Methods 0.000 abstract description 10
- 239000004332 silver Substances 0.000 abstract description 10
- 229910052709 silver Inorganic materials 0.000 abstract description 10
- 238000009835 boiling Methods 0.000 abstract description 6
- 229920003169 water-soluble polymer Polymers 0.000 abstract description 4
- 230000015572 biosynthetic process Effects 0.000 abstract description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 12
- 239000003795 chemical substances by application Substances 0.000 description 9
- 239000012224 working solution Substances 0.000 description 7
- ZNBNBTIDJSKEAM-UHFFFAOYSA-N 4-[7-hydroxy-2-[5-[5-[6-hydroxy-6-(hydroxymethyl)-3,5-dimethyloxan-2-yl]-3-methyloxolan-2-yl]-5-methyloxolan-2-yl]-2,8-dimethyl-1,10-dioxaspiro[4.5]decan-9-yl]-2-methyl-3-propanoyloxypentanoic acid Chemical compound C1C(O)C(C)C(C(C)C(OC(=O)CC)C(C)C(O)=O)OC11OC(C)(C2OC(C)(CC2)C2C(CC(O2)C2C(CC(C)C(O)(CO)O2)C)C)CC1 ZNBNBTIDJSKEAM-UHFFFAOYSA-N 0.000 description 5
- 125000000217 alkyl group Chemical group 0.000 description 5
- 229910000378 hydroxylammonium sulfate Inorganic materials 0.000 description 5
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 4
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 150000002430 hydrocarbons Chemical group 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 239000012670 alkaline solution Substances 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- UPBDXRPQPOWRKR-UHFFFAOYSA-N furan-2,5-dione;methoxyethene Chemical compound COC=C.O=C1OC(=O)C=C1 UPBDXRPQPOWRKR-UHFFFAOYSA-N 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920001467 poly(styrenesulfonates) Polymers 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 1
- 239000003929 acidic solution Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000008064 anhydrides Chemical group 0.000 description 1
- 229920006318 anionic polymer Polymers 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000006184 cosolvent Substances 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 150000002443 hydroxylamines Chemical class 0.000 description 1
- 229920003063 hydroxymethyl cellulose Polymers 0.000 description 1
- 229940031574 hydroxymethyl cellulose Drugs 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
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
- G03C5/305—Additives other than developers
-
- 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
- G03C5/264—Supplying of photographic processing chemicals; Preparation or packaging thereof
- G03C5/266—Supplying of photographic processing chemicals; Preparation or packaging thereof of solutions or concentrates
Definitions
- a Synthetic, Water-Soluble Polymer having a hydrocar- 252/364, 260/785 23 bon backbone is employed as a dispersing agent in dispersions in water of a solvent for high-boiling, water- 5 References Cited immiscible vehicles useful in the photographic solvent- UNITED STATES PATENTS dispersion technique for the formation of coupler- 2 286 2 9/1942 L 96/11 containing photographic silver halide elements.
- the present invention relates to color photographic processing, and more particularly relates to developer solutions, solution concentrates, and methods for color development.
- One system of silver halide color photography employs silver halide photographic elements which have a plurality of silver halide layers, each layer having a photographic color coupler dispersed therein by the solvent dispersion technique.
- This technique involves dispersing, in a silver halide emulsion, very fine droplets of a high-boiling, water-immiscible liquid vehicle such as tricresyl phosphate, in which is dissolved a color coupler.
- a high-boiling, water-immiscible liquid vehicle such as tricresyl phosphate
- Color development working solutions ordinarily include, in addition to a p-phenylenediamine color developer and other photographic adjuvants, a solvent for the droplets of the high-boiling, water-immiscible vehicle referred to above.
- solvents such as aromatic alcohols (e.g., benzyl alcohol) and the like
- aromatic alcohols e.g., benzyl alcohol
- dye-forming reaction e.g., benzyl alcohol
- kits may contain two or more separately packaged compositions.
- One such composition may include a concentrated aqueous acidic solution of a photographic p-phenylenediamine developer.
- Another package may contain a concentrated aqueous alkaline solution, antioxidants, and the like.
- a third package may contain, in concentrated form, the solvent referred to above. Since this solvent is a solvent for the highboiling, water-immiscible, coupler-containing vehicles used in the solvent dispersion technique, such solvents ordinarily exhibit a very limited solubility in water.
- benzyl alcohol or other solvents are provided in concentrated form as aqueous dispersions using, as dispersing agents, such materials as cellulose derivatives (e.g., hydroxymethyl cellulose), water-soluble polymeric carbohydrates and watersoluble polymeric amides (Belgian Pat. No. 727,705).
- dispersing agents such materials as cellulose derivatives (e.g., hydroxymethyl cellulose), water-soluble polymeric carbohydrates and watersoluble polymeric amides (Belgian Pat. No. 727,705).
- the invention relates to a concentrated dispersion in water of a solvent selected from the group consisting of aromatic alcohols, alkyl glycol ethers, aryl glycol ethers, alkyl polyglycol ethers and aryl polyglycol ethers, which solvent is soluble in water to an extent of about 10 g/l to about g/l.
- the dispersion includes a dispersing agent which is a synthetic, watersoluble polymer prepared from ethylenically unsaturated monomers and having essentially a hydrocarbon backbone.
- the dispersing agent is an anionic polymer, and in its most preferred embodiment the dispersing agent is a water-soluble addition polymer hydrolyzate having recurring units of the formula such as, for example, hydrolyzates of copolymers of maleic anhydride and ethylenically unsaturated comonomers such as styrene, ethylene and methyl vinyl ether.
- the polymeric dispersing agents of the invention are prepared from ethylenically unsaturated monomers such as maleic anhydride, and accordingly have a backbone which consists essentially of a hydrocarbon chain.
- the polymeric dispersing agents are water-soluble; that is, they are immediately soluble in water (e.g., polyvinyl alcohol, sulfonated polystyrene, etc.) or can be made soluble in water by hydrolysis of the pendant groups thereof (as for example the maleic anhydride copolymers referred to above).
- water soluble refers to polymers of both types.
- the polymers of the invention further are preferably anionic; that is, the polymers will dissolve and ionize in water to form a negatively charged polymeric species.
- examples of such polymers are the maleic anhydride copolymers referred to above, sulfonated polystyrene, and copolymers of vinyl sulfonic acid.
- water-soluble addition polymer hydrolyzates of the formula set forth above, which polymers may be formed from maleic anhydride and ethylenically unsaturated comonomers by techniques known to the art. Of particular importance are the copolymers of maleic anhydride with styrene, ethylene and methyl vinyl ether. The mer ratio of units derived from maleic anhydride to units derived from other ethylenically unsaturated monomers must be such as to render the hydrolyzate of such polymers readily soluble in water. As is known to the art, maleic anhydride copolymers themselves generally have limited solubility in water. Upon addition of such polymers to water, hydrolysis of the anhydride groups of the maleic anhydride mer units is believed to occur, thereby rendering the polymers highly soluble in water.
- the solvents of the invention include aromatic alcohols such as benzyl alcohol, as reported in British Pat. No. 546,347.
- aromatic alcohols such as benzyl alcohol, as reported in British Pat. No. 546,347.
- alkyl glycol ethers, aryl glycol ethers, alkyl polyglycol ethers or aryl polyglycol ethers such as are described in the copending application Ser. No. 186,675 of H. Santemma and R. Fisch entitled Color Photographic Developing Solution.
- the latter solvents are characterized by the formula wherein R is a C C alkyl group or an aryl group having no more than 10 carbon atoms, R and R each independently represent a hydrogen atom or a C C alkyl group with the proviso that at least one of R and R is hydrogen, and n is an integer of from one to five.
- the concentrates of the invention employ the solvents as described above in a concentration which exceeds the miscibility of the solvent in water.
- the weight ratio of water to dispersed solvent is desirably maintained between about Ill and 25/l.
- the dispersions of the invention either do not separate into separate layers or, if some tendency to form layers occurs, the solvent can be readily redispersed upon moderate agitation.
- the dispersed concentrates of the invention may additionally include such photographic adjuvants as color developers of the pphenylenediamine type, black and white developers such as hydroquinone, and hydroxylamine salts such as hydroxylamine sulfate.
- the dispersed concentrates of the invention may include hydroxylamine sulfate in a quantity limited only by the solubility of this compound in the concentrate. Preferably, however, hydroxylamine sulfate is employed in a salt/water weight ratio of from about 0.1/100 to about 33/100.
- the concentrates of the present invention may be easily prepared by incorporating a suitable quantity of dispersing agent in water, and then adding thereto, with vigorous agitation, a selected solvent such as benzyl alcohol.
- the concentrates of the invention are preferably adjusted to about neutral pH, e.g., in the range of from about pH 5 to about pH 9.
- the dispersed concentrate of the invention is combined with the ingredients of other packages thereof such as an aqueous, acidic developing agent concentrate and an aqueous, alkaline solution concentrate, to form, with water, a photographic color developer working solution.
- the poorly-soluble solvents of the invention, in dispersed form, are readily dissolved during preparation of the working solution, thereby permitting the working solu- 6
- replenisher kits which are employed to provide replenisher solutions; i.e., solutions which are used to replenish depleted photographic color processing working solutions.
- EXAMPLE 1 A three-package color development replenisher kit was prepared as follows: Part A Hydroxylamine sulfate2.l g.
- Maleie anhydride-methyl vinyl ether copolymer (Gantrez AN 169, a trademarked product of General Aniline and Film Corporation) (10 percent aqueous solution)2.0 ml.
- Sequestering agent (Antical-3, a product of Eastman Kodak Co.)1.6 g.
- Part A above was in the form of a practically stable dispersion.
- Parts A, B and C were added in order to 800 ml. of water to form, upon further dilution to 1,000 ml., and with minimal stirring, a photographic color developer replenisher solution.
- EXAM PLE 2 A two-package photographic color developer replenisher kit was prepared as follows: Part A Potassium hydroxide (45 percent aqueous solution) Boric acid 118.4 g.
- Part B Developing agent (4-amino-N-ethyl-N-(B- methanesulfonamido ethyl)-m-toluidine sesquisulfate)50.0 g.
- EXAMPLE 3 The color development kit of Example 2 was duplicated except that in part B thereof, a copolymer of styrene and maleic anhydride (SMA, Monsanto Chemical Company) percent aqueous solution (8.0 ml.) was substituted for the 9.0 ml. of maleic anhydridemethyl vinyl ether copolymer. Similar results were obtained.
- SMA styrene and maleic anhydride
- EXAMPLE 4 The photographic color development kit of Example 1 was duplicated except that in part A thereof, 2.0 ml. of a 10 percent aqueous solution of the copolymer of ethylene and maleic anhydride (EMA, Monsanto Chemical Company) was substituted for the 2.0 ml. of maleic anhydride-methyl vinyl ether copolymer employed therein. Similar results were obtained.
- EMA copolymer of ethylene and maleic anhydride
- a concentrated photographic developing agent dispersion in water capable of dilution to a developing solution, comprising:
- a solvent selected from the group consisting of aromatic alcohols, alkyl glycol ethers, aryl glycol ethers, alkyl polyglycol ethers and aryl polyglycol ethers, which solvent has a solubility limit in water of from about 10 g/l to about 100 g/l,
- a dispersing agent which is a synthetic water soluble polymer prepared from ethylentically unsaturated monomers and having essentially a hydrocarbon backbone
- At least one photographic developing agent selected from hydroxylamine sulfate or a paraphenylene diamine type developer.
- dispersing agent is a water-soluble addition polymer hydrolyzate having recurring units of the formula 4.
- dispersing agent is the copolymer of maleic anhydride and styrene.
- a concentrated dispersion in water capable of use in photographic developer kits comprising a solvent selected from the group consisting of aromatic alcohols, alkyl glycol ethers, aryl glycol ethers alkyl polyglycol ethers and aryl polyglycol ethers, which solvent has a solubility in water of from about 10 g/l to about 100 g/l, said dispersion including, as a dispersing agent, a water-soluble addition polymer hydrolyzate having recurring units of the formula and at least one photographic developing agent selected from the group of hydroxylamine sulfate or a para-phenylene diamine type developer.
- the concentrated dispersion of claim 7 in which the solvent is present in the dispersion in a ratio to water of from about 12 g/l00 ml to about 50 g/lOO ml, and the dispersing agent is present in a ratio to water of from about 0.45 g/l00 ml to 1.0 g/l00 ml.
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- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Abstract
A synthetic, water-soluble polymer having a hydrocarbon backbone is employed as a dispersing agent in dispersions in water of a solvent for high-boiling, water-immiscible vehicles useful in the photographic solvent-dispersion technique for the formation of coupler-containing photographic silver halide elements.
Description
, O i 5 United States Patent 1191 1111 3,785,824 Fisch 1 Jan. 15, 1974 [54] PHOTOGRAPHIC AQUEOUS DISPERSION 1,976,679 10/1934 Fikentscher ct al. 252/356 CONCENTRATES 3,141,897 7/1964 Crecelius et a1. 252/356 3,385,834 5/1968 Merijan 252/356 Inventor: Rlchard Flsch, Paul. 2,645,615 7/1953 POllOk 252/356 3,589,902 6/1971 Himmelmann et a1. 96/66 [73] Assignee. xmnesota L/hmgg nd S P 1 3,615,497 10/1971 Fassbender 96/66.1 F 3,649,287 3/1972 De Pauw et al. 96/100 Minn.
[22] Filed: Sept. 24, 1971 Primary ExaminerJ. Travis Brown Assistant Examiner-Richard L. Schilling [21] Appl' 183703 AttorneyAlexander, Sell, Steldt & Delahunt [52] US. Cl. 96/66 R, 96/66.l 51 Int. Cl G03c 5/30 [57] ABSTRACT 58 Field of Search 96/66, 114, 66.1; A Synthetic, Water-Soluble Polymer having a hydrocar- 252/364, 260/785 23 bon backbone is employed as a dispersing agent in dispersions in water of a solvent for high-boiling, water- 5 References Cited immiscible vehicles useful in the photographic solvent- UNITED STATES PATENTS dispersion technique for the formation of coupler- 2 286 2 9/1942 L 96/11 containing photographic silver halide elements.
owe 3,4l8,1 18 12/1968 Thommes et a]. 96/20 11 Claims, N0 Drawings PHOTOGRAPHIC AQUEOUS DISPERSION CONCENTRATES The present invention relates to color photographic processing, and more particularly relates to developer solutions, solution concentrates, and methods for color development.
One system of silver halide color photography employs silver halide photographic elements which have a plurality of silver halide layers, each layer having a photographic color coupler dispersed therein by the solvent dispersion technique. This technique involves dispersing, in a silver halide emulsion, very fine droplets of a high-boiling, water-immiscible liquid vehicle such as tricresyl phosphate, in which is dissolved a color coupler. Reference is made to U. S. Pat. Nos. 2,332,027 and 2,801,170. During color development of the so-described silver halide element, silver halide is reduced by the developing agent to silver, and the developing agent is oxidized. The oxidation product of the developing agent couples, i.e., reacts, with the color coupler which is'included within the very fine droplets dispersed in the silver halide emulsion, to form a dye.
Color development working solutions ordinarily include, in addition to a p-phenylenediamine color developer and other photographic adjuvants, a solvent for the droplets of the high-boiling, water-immiscible vehicle referred to above. Such solvents (such as aromatic alcohols (e.g., benzyl alcohol) and the like) are believed to promote access of the oxidized developer to the couplers, thereby promoting the dye-forming reaction and enabling dye images of the proper density to be obtained. Reference is made to British Pat. No. 546,347.
Color developer working solutions are often prepared by the user from photographic developer kits, the user merely combining and diluting the kit contents to form the desired developer solution. Such kits may contain two or more separately packaged compositions. One such composition, for example, may include a concentrated aqueous acidic solution of a photographic p-phenylenediamine developer. Another package may contain a concentrated aqueous alkaline solution, antioxidants, and the like. A third package may contain, in concentrated form, the solvent referred to above. Since this solvent is a solvent for the highboiling, water-immiscible, coupler-containing vehicles used in the solvent dispersion technique, such solvents ordinarily exhibit a very limited solubility in water. In order to permit such solvents to be incorporated into concentrates for use in kit form, and yetto promote rapid dissolution of such solvents during preparation of a photographic developer working solution, it has been proposed that such solvents be incorporated in a con-- centrated water solution which also includes a simple glycol co-solvent to promote solubility (U. S. Pat. No. 3,574,619).
In another method, benzyl alcohol or other solvents are provided in concentrated form as aqueous dispersions using, as dispersing agents, such materials as cellulose derivatives (e.g., hydroxymethyl cellulose), water-soluble polymeric carbohydrates and watersoluble polymeric amides (Belgian Pat. No. 727,705). By virtue of the fact that such dispersing agents are naturally-occurring materials, a variation in the properties thereof can be expected to lead to inconsistent dispersion characteristics and thus to inconsistent photographic developing characteristics in photographic dcveloper working solutions. In addition, cellulosic materials are often subject to certain chemical reactions (e.g., hydrolysis), causing degradation thereof.
It is an object of the present invention to provide a storage-stable dispersed concentrate of a solvent for high-boiling, water-immiscible liquid vehicles employed in the solvent dispersion technique.
It is another object of the invention to provide a dispersed concentrate of a solvent for the high-boiling, water-immiscible liquid vehicles employed in the solvent dispersion technique which employs a storagestable, photographically-acceptable dispersing agent for the solvent.
Briefly, the invention relates to a concentrated dispersion in water of a solvent selected from the group consisting of aromatic alcohols, alkyl glycol ethers, aryl glycol ethers, alkyl polyglycol ethers and aryl polyglycol ethers, which solvent is soluble in water to an extent of about 10 g/l to about g/l. The dispersion includes a dispersing agent which is a synthetic, watersoluble polymer prepared from ethylenically unsaturated monomers and having essentially a hydrocarbon backbone. In a preferred embodiment, the dispersing agent is an anionic polymer, and in its most preferred embodiment the dispersing agent is a water-soluble addition polymer hydrolyzate having recurring units of the formula such as, for example, hydrolyzates of copolymers of maleic anhydride and ethylenically unsaturated comonomers such as styrene, ethylene and methyl vinyl ether.
The polymeric dispersing agents of the invention, as noted, are prepared from ethylenically unsaturated monomers such as maleic anhydride, and accordingly have a backbone which consists essentially of a hydrocarbon chain. The polymeric dispersing agents are water-soluble; that is, they are immediately soluble in water (e.g., polyvinyl alcohol, sulfonated polystyrene, etc.) or can be made soluble in water by hydrolysis of the pendant groups thereof (as for example the maleic anhydride copolymers referred to above). The term water soluble" as used herein refers to polymers of both types. The polymers of the invention further are preferably anionic; that is, the polymers will dissolve and ionize in water to form a negatively charged polymeric species. Examples of such polymers are the maleic anhydride copolymers referred to above, sulfonated polystyrene, and copolymers of vinyl sulfonic acid.
Most preferred as dispersing agents in the present invention, however, are water-soluble addition polymer hydrolyzates of the formula set forth above, which polymers may be formed from maleic anhydride and ethylenically unsaturated comonomers by techniques known to the art. Of particular importance are the copolymers of maleic anhydride with styrene, ethylene and methyl vinyl ether. The mer ratio of units derived from maleic anhydride to units derived from other ethylenically unsaturated monomers must be such as to render the hydrolyzate of such polymers readily soluble in water. As is known to the art, maleic anhydride copolymers themselves generally have limited solubility in water. Upon addition of such polymers to water, hydrolysis of the anhydride groups of the maleic anhydride mer units is believed to occur, thereby rendering the polymers highly soluble in water.
The solvents of the invention include aromatic alcohols such as benzyl alcohol, as reported in British Pat. No. 546,347. Of particular interest are alkyl glycol ethers, aryl glycol ethers, alkyl polyglycol ethers or aryl polyglycol ethers, such as are described in the copending application Ser. No. 186,675 of H. Santemma and R. Fisch entitled Color Photographic Developing Solution. The latter solvents are characterized by the formula wherein R is a C C alkyl group or an aryl group having no more than 10 carbon atoms, R and R each independently represent a hydrogen atom or a C C alkyl group with the proviso that at least one of R and R is hydrogen, and n is an integer of from one to five. The concentrates of the invention employ the solvents as described above in a concentration which exceeds the miscibility of the solvent in water. The weight ratio of water to dispersed solvent is desirably maintained between about Ill and 25/l. The dispersions of the invention either do not separate into separate layers or, if some tendency to form layers occurs, the solvent can be readily redispersed upon moderate agitation.
In addition to the solvent referred to above, and a dispersing agent therefor, the dispersed concentrates of the invention may additionally include such photographic adjuvants as color developers of the pphenylenediamine type, black and white developers such as hydroquinone, and hydroxylamine salts such as hydroxylamine sulfate. The dispersed concentrates of the invention may include hydroxylamine sulfate in a quantity limited only by the solubility of this compound in the concentrate. Preferably, however, hydroxylamine sulfate is employed in a salt/water weight ratio of from about 0.1/100 to about 33/100.
The concentrates of the present invention may be easily prepared by incorporating a suitable quantity of dispersing agent in water, and then adding thereto, with vigorous agitation, a selected solvent such as benzyl alcohol. The concentrates of the invention are preferably adjusted to about neutral pH, e.g., in the range of from about pH 5 to about pH 9.
In use in photographic kit form, the dispersed concentrate of the invention is combined with the ingredients of other packages thereof such as an aqueous, acidic developing agent concentrate and an aqueous, alkaline solution concentrate, to form, with water, a photographic color developer working solution. The poorly-soluble solvents of the invention, in dispersed form, are readily dissolved during preparation of the working solution, thereby permitting the working solu- 6 Although the above description has been directed primarily to photographic color developing solution kits for producing working developer solutions, it will be understood that this description also refers to replenisher kits which are employed to provide replenisher solutions; i.e., solutions which are used to replenish depleted photographic color processing working solutions.
The invention may be more readily understood by reference to the following illustrative, non-limiting examples:
EXAMPLE 1 A three-package color development replenisher kit was prepared as follows: Part A Hydroxylamine sulfate2.l g.
Benzyl alcohol-12.6 ml.
Maleie anhydride-methyl vinyl ether copolymer (Gantrez AN 169, a trademarked product of General Aniline and Film Corporation) (10 percent aqueous solution)2.0 ml.
Water to20.0 ml.
Part B Potassium carbonate-40.3 g.
Sodium sulfite--2.3 g.
Potassium bromide-0.16 g.
Sequestering agent (Antical-3, a product of Eastman Kodak Co.)1.6 g.
Water to57.5 ml.
Part C Sodium sulfite3.0 g. Developing agent (4-amino-N-ethyl-N-(B- methanesulfonamido ethyl)-m-toluidine sesquisulfate)5.0 g. Water to about-l3.0 ml.
Part A above was in the form of a practically stable dispersion. Parts A, B and C were added in order to 800 ml. of water to form, upon further dilution to 1,000 ml., and with minimal stirring, a photographic color developer replenisher solution.
EXAM PLE 2 A two-package photographic color developer replenisher kit was prepared as follows: Part A Potassium hydroxide (45 percent aqueous solution) Boric acid 118.4 g.
Sodium sulfite 6.78 g.
Water to 325 ml.
Part B Developing agent (4-amino-N-ethyl-N-(B- methanesulfonamido ethyl)-m-toluidine sesquisulfate)50.0 g.
Sodium sulfite2.24 g.
Benzyl alcohol-30.0 ml.
Maleic anhydride-methyl vinyl ether copolymer (Gantrez AN 149, a product of General Aniline and Film Corp.), 10 percent aqueous solution9.0 ml.
Water to200 ml.
The contents of parts A and B of this example, when combined and diluted to 10 l. with water, provide a photographic color developer replenisher solution.
EXAMPLE 3 The color development kit of Example 2 was duplicated except that in part B thereof, a copolymer of styrene and maleic anhydride (SMA, Monsanto Chemical Company) percent aqueous solution (8.0 ml.) was substituted for the 9.0 ml. of maleic anhydridemethyl vinyl ether copolymer. Similar results were obtained.
EXAMPLE 4 The photographic color development kit of Example 1 was duplicated except that in part A thereof, 2.0 ml. of a 10 percent aqueous solution of the copolymer of ethylene and maleic anhydride (EMA, Monsanto Chemical Company) was substituted for the 2.0 ml. of maleic anhydride-methyl vinyl ether copolymer employed therein. Similar results were obtained.
What is claimed is:
l. A concentrated photographic developing agent dispersion in water, capable of dilution to a developing solution, comprising:
a. a solvent selected from the group consisting of aromatic alcohols, alkyl glycol ethers, aryl glycol ethers, alkyl polyglycol ethers and aryl polyglycol ethers, which solvent has a solubility limit in water of from about 10 g/l to about 100 g/l,
b. a dispersing agent which is a synthetic water soluble polymer prepared from ethylentically unsaturated monomers and having essentially a hydrocarbon backbone,
c. and at least one photographic developing agent selected from hydroxylamine sulfate or a paraphenylene diamine type developer.
2. The dispersion of claim 1 wherein said polymeric dispersing agent is anionic.
3. The dispersion of claim 1 wherein said dispersing agent is a water-soluble addition polymer hydrolyzate having recurring units of the formula 4. The dispersion of claim 3 wherein said dispersing agent is the copolymer of maleic anhydride and styrene.
5. The dispersion of claim 3 wherein said dispersing agent is the copolymer of maleic anhydride and ethylene.
6. The dispersion of claim 3 wherein said dispersing agent is the copolymer of maleic anhydride and methyl vinyl ether.
7. The concentrated dispersion of claim 1 in which the solvent is present in the dispersion in a ratio to water from about 12 g/ ml to about 50 g/100 ml, and the dispersing agent is present in a ratio to water of from about 0.45 g/l00 ml. to 1.0 g/l00 ml.
8. A concentrated dispersion in water capable of use in photographic developer kits, said dispersion comprising a solvent selected from the group consisting of aromatic alcohols, alkyl glycol ethers, aryl glycol ethers alkyl polyglycol ethers and aryl polyglycol ethers, which solvent has a solubility in water of from about 10 g/l to about 100 g/l, said dispersion including, as a dispersing agent, a water-soluble addition polymer hydrolyzate having recurring units of the formula and at least one photographic developing agent selected from the group of hydroxylamine sulfate or a para-phenylene diamine type developer.
9. The dispersion of claim 8 wherein said solvent is benzyl alcohol.
10. The dispersion of claim 8 wherein said solvent is ethylene glycol monophenylether.
11. The concentrated dispersion of claim 7 in which the solvent is present in the dispersion in a ratio to water of from about 12 g/l00 ml to about 50 g/lOO ml, and the dispersing agent is present in a ratio to water of from about 0.45 g/l00 ml to 1.0 g/l00 ml.
Um'mm swims m'mm OFFICE CERTIFICATE OF CORRECTIGN tent No- 3,785,82 7 1mm January 15, 19714 m fl y Richard s. Fisch Iris h ertified that are: sweats in the dbbvvidentified patent and that-paid Letters Patent are hereby cormctad amahm below:
001. 6-, line 13, after "water insert of--.
. col-. 6; line &1, "7'1" sho uld read --8--.
, Signd and s e'aled "this 19th day of November 1974.
(SEAL) Attest MCCOY .M. GIBSON JR; v c. MARSHALL DANN Attesting Officer ,Commissi'oner of Patents
Claims (10)
- 2. The dispersion of claim 1 wherein said polymeric dispersing agent is anionic.
- 3. The dispersion of claim 1 wherein said dispersing agent is a water-soluble addition polymer hydrolyzate having recurring units of the formula
- 4. The dispersion of claim 3 wherein said dispersing agent is the copolymer of maleic anhydride and styrene.
- 5. The dispersion of claim 3 wherein said dispersing agent is the copolymer of maleic anhydride and ethylene.
- 6. The dispersion of claim 3 wherein said dispersing agent is the copolymer of maleic anhydride and methyl vinyl ether.
- 7. The concentrated dispersion of claim 1 in which the solvent is present in the dispersion in a ratio to water of from about 12 g/100 ml to about 50 g/100 ml, and the dispersing agent is present in a ratio to water of from about 0.45 g/100 ml. to 1.0 g/100 ml.
- 8. A concentrated dispersion in water capable of use in photographic developer kits, said dispersion comprising a solvent selected from the group consisting of aromatic alcohols, alkyl glycol etherS, aryl glycol ethers alkyl polyglycol ethers and aryl polyglycol ethers, which solvent has a solubility in water of from about 10 g/l to about 100 g/l, said dispersion including, as a dispersing agent, a water-soluble addition polymer hydrolyzate having recurring units of the formula
- 9. The dispersion of claim 8 wherein said solvent is benzyl alcohol.
- 10. The dispersion of claim 8 wherein said solvent is ethylene glycol monophenylether.
- 11. The concentrated dispersion of claim 7 in which the solvent is present in the dispersion in a ratio to water of from about 12 g/100 ml to about 50 g/100 ml, and the dispersing agent is present in a ratio to water of from about 0.45 g/100 ml to 1.0 g/100 ml.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US18370371A | 1971-09-24 | 1971-09-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3785824A true US3785824A (en) | 1974-01-15 |
Family
ID=22673972
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US00183703A Expired - Lifetime US3785824A (en) | 1971-09-24 | 1971-09-24 | Photographic aqueous dispersion concentrates |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3785824A (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3929485A (en) * | 1973-07-26 | 1975-12-30 | Fuji Photo Film Co Ltd | Dispersion of silver halide developing agent with surface active polymers of maleic acid half esters |
| US4081281A (en) * | 1972-02-18 | 1978-03-28 | Agfa-Gevaert N.V. | Developing low fogged, direct-positive silver halide emulsion with an energetic developer free from halide ions |
| FR2420153A1 (en) * | 1978-03-15 | 1979-10-12 | Minnesota Mining & Mfg | CONCENTRATED LIQUID COMPOSITIONS OF DEVELOPERS AND THEIR APPLICATION TO COLOR PHOTOGRAPHY |
| US4232113A (en) * | 1979-03-14 | 1980-11-04 | Minnesota Mining And Manufacturing Company | Liquid concentrated developer composition, and confection ready to mix with water including it, for use in color photography |
| US4615971A (en) * | 1983-03-03 | 1986-10-07 | Agfa-Gevaert Aktiengesellschaft | Photographic developer composition |
| EP0204372A1 (en) * | 1985-06-07 | 1986-12-10 | Chemco, Inc. | Method for the preparation of photographic bath concentrates in paste form, method for processing such concentrates to give ready-for-use photographic processing baths, an apparatus suitable for such processing and a pump arrangement appertaining to this apparatus |
| US4770979A (en) * | 1981-12-24 | 1988-09-13 | Konishiroku Photo Industry Co., Ltd. | Developer composition |
| US20080122915A1 (en) * | 2006-08-24 | 2008-05-29 | Eastman Kodak Company | Polymeric colorant-based ink compositions |
-
1971
- 1971-09-24 US US00183703A patent/US3785824A/en not_active Expired - Lifetime
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4081281A (en) * | 1972-02-18 | 1978-03-28 | Agfa-Gevaert N.V. | Developing low fogged, direct-positive silver halide emulsion with an energetic developer free from halide ions |
| US3929485A (en) * | 1973-07-26 | 1975-12-30 | Fuji Photo Film Co Ltd | Dispersion of silver halide developing agent with surface active polymers of maleic acid half esters |
| FR2420153A1 (en) * | 1978-03-15 | 1979-10-12 | Minnesota Mining & Mfg | CONCENTRATED LIQUID COMPOSITIONS OF DEVELOPERS AND THEIR APPLICATION TO COLOR PHOTOGRAPHY |
| US4232113A (en) * | 1979-03-14 | 1980-11-04 | Minnesota Mining And Manufacturing Company | Liquid concentrated developer composition, and confection ready to mix with water including it, for use in color photography |
| US4770979A (en) * | 1981-12-24 | 1988-09-13 | Konishiroku Photo Industry Co., Ltd. | Developer composition |
| US4615971A (en) * | 1983-03-03 | 1986-10-07 | Agfa-Gevaert Aktiengesellschaft | Photographic developer composition |
| EP0118071A3 (en) * | 1983-03-03 | 1986-10-15 | Agfa-Gevaert Aktiengesellschaft | Photographic developer |
| EP0204372A1 (en) * | 1985-06-07 | 1986-12-10 | Chemco, Inc. | Method for the preparation of photographic bath concentrates in paste form, method for processing such concentrates to give ready-for-use photographic processing baths, an apparatus suitable for such processing and a pump arrangement appertaining to this apparatus |
| US20080122915A1 (en) * | 2006-08-24 | 2008-05-29 | Eastman Kodak Company | Polymeric colorant-based ink compositions |
| US7732509B2 (en) * | 2006-08-24 | 2010-06-08 | Eastman Kodak Company | Polymeric colorant-based ink compositions |
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