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
  • G03C8/00—Diffusion transfer processes or agents therefor; Photosensitive materials for such processes
  • G03C8/02—Photosensitive materials characterised by the image-forming section
  • G03C8/04—Photosensitive materials characterised by the image-forming section the substances transferred by diffusion consisting of inorganic or organo-metallic compounds derived from photosensitive noble metals
  • G03C8/06—Silver salt diffusion transfer
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F8/00—Chemical modification by after-treatment
  • C08F8/30—Introducing nitrogen atoms or nitrogen-containing groups
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F8/00—Chemical modification by after-treatment
  • C08F8/44—Preparation of metal salts or ammonium salts
• • G—PHYSICS
  • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
  • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
  • G03C1/00—Photosensitive materials
  • G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
  • G03C1/04—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with macromolecular additives; with layer-forming substances
  • G03C1/053—Polymers obtained by reactions involving only carbon-to-carbon unsaturated bonds, e.g. vinyl polymers
• • 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
  • G03C8/00—Diffusion transfer processes or agents therefor; Photosensitive materials for such processes
• • 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
  • G03C8/00—Diffusion transfer processes or agents therefor; Photosensitive materials for such processes
  • G03C8/24—Photosensitive materials characterised by the image-receiving section
  • G03C8/26—Image-receiving layers
  • G03C8/28—Image-receiving layers containing development nuclei or compounds forming such nuclei
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F2800/00—Copolymer characterised by the proportions of the comonomers expressed
  • C08F2800/10—Copolymer characterised by the proportions of the comonomers expressed as molar percentages
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10S526/00—Synthetic resins or natural rubbers -- part of the class 520 series
  • Y10S526/923—Ethylenic monomers containing at least one salt group

Definitions

• Peptizers for silver halide dispersions in preparation of photographic emulsions are hydrophilic polymers with quaternary nitrogen atoms bonded to the polymer through ether linkages.
• Specific polymers of the useful class include units having formulae wherein R and R are alkyl or aryl or together complete a 5 or 6 member heterocyclic ring, R is allkyl, R is alkylene, A is acid anion, and is the repeating unit of a polysaccharide.
• This invention relates to photography and more particularly to polymeric materials compatible with photographic emulsions, and methods of preparing photographic emulsions utilizing certain polymeric materials.
• the initial steps in the preparation of a photographic silver halide emulsion are usually precipitation and ripening.
• a peptizing agent to be effective, plays a significant role in each of these steps.
• Gelatin is generally used as the peptizer in commercial emulsions, but certain disadvantages are associated with its use. Gelatin is susceptible to attack by molds and bacteria. Also, as a further consequence of the natural origin of gelatin, a supply from a given source often varies in properties from time to time. Finally, the use of gelatin restricts the type of crystal irregularities obtainable by a given emulsion precipitation procedure to those types which are related to the inherent colloid-chemical nature of gelatin.
• One object of our invention is to provide new photo graphic emulsions of excellent stability. Another object of our invention is to provide novel silver halide dispersions of excellent stability. Still another object of our invention is to provide silver halide grains which possess photographically desirable dimensional and crystallographic properties. A further object of our invention is to provide a novel photographic element containing therein a poly- 3,425,836 Patented Feb. 4, 1969 meric gelatin substitute. Another object of our invention is to provide a novel process for the preparation of photographic elements of high stability containing therein polymeric materials.
• Still another object of our invention is to provide polymeric materials which effectively peptize the silver halide formed by the double decomposition reaction from aqueous solutions of alkalid halide salts and solutions of soluble silver salts, either in the presence of or absence of ammonia.
• Another object of our invention is to provide novel photographic emulsions which exhibit good physical development characteristics.
• Another ob ject of our invention is to provide new photographic emulsions which impart a black-toning effect to silver obtained by physical development. Other objects will become obbious in the following disclosure.
• light sensitive silver halide salts are peptized with a hydrophilic polymer having a plurality of quaternary nitrogen atoms chemically bonded to the polymer through ether (O) linkages, preferably oxyalkyl linkages such as oxymethyl.
• ether (O) linkages preferably oxyalkyl linkages such as oxymethyl.
• ether linkages preferably oxyalkyl, e.g., oxymethyl
• hydrophilic polymers employed in our invention have repeating units represented by the following general formula:
• R and R each represent a substituent selected from the group consisting of alkyl radicals having 1 to 8 carbon atoms, such as methyl, ethyl, propyl, butyl, hexyl or octyl; an aryl group such as phenyl or naphthyl; and, R and R taken together, represent the atoms, such as C, N, O or S, necessary to complete a heterocyclic ring composed of to 6 atoms; R represents a substituent selected from the group consisting of alkyl radicals having 1 to 6 carbon atoms, such as methyl, ethyl, propyl, butyl, amyl or hexyl; R represents a bivalent organic radical, e.g., an alkylene group of 1 to 5 carbon atoms, such as ethylene, propylene, butylene, pentylene and, preferably, methylene; and A represents an acid anion compatible with the formation of a quaternary salt,
• the polymer is free from any substituents which might have a detrimental effect on photographic silver halide emulsions.
• These polymers may be homopolymers or interpolymers having, in addition to the repeating units defined above, any campatible repeating unit or various repeating units which are not detrimental to photographic silver halide emulsions.
• Typical repeating units which may be present in these polymers have the following general formula:
• A, B, D and E represent hydrogen, and the remainder, if any, each are selected from the group consisting of hydrogen; alkyl such as methyl, ethyl, propyl or butyl; aryl such as phenyl; acyl such as acetyl, propionyl, and butyryl; acyloxy such as actyloxy and propionyloxy; cyano; diacylimido; alkoxy such as methoxy, ethoxy, propoxy, and butoxy; aryloxy such as phenoxy; carbalkoxy; carbamyl; carboxy, and the like.
• the ratio of all the repeating units of the polymer to repeating units corresponding to Formula 1 above is less than 5:1, and preferably is from 4:1 to 1:1.
• copolymers of vinyl alcohol which may also contain minor propor- Eormula2 I I I wherein 1 represents the repeating unit of a hydrophilic polysaccharide such as amylose or a far hydrolyzed cellulose ester, e.g., cellulose acetate hydrolyzed to an acetyl content of 13 to 26%; and R R R R R and A have the same meaning given above. It is not necessary that each repeating unit of the polysaccharide contain quaternary nitrogen substituents as described in Formula 2.
• any given repeating unit of the polysaccharide may contain more than one of the quaternary nitrogen substituents.
• the ratio of total repeating units to repeating units of the type described in Formula 2 is less than 5:1 and preferably is from 4:1 to 1:3.
• the polysaccharide derivatives employed herein are preferably free from any substituents which would exert a detrimental effect on emulsions in which they are incorporated.
• the polymers employed in this invention may be prepared in any convenient manner, such as by reacting a suitable hydroxyl containing polymer with an alkoxyalkyl N,N-disubstituted amine, followed by quaternization of the amino group.
• the substituents on the nitrogen atom may be the same as R and R defined above.
• a neutral emulsion was prepared in the following manner. Twenty ml. of an aqueous solution containing 3.82 g. of silver nitrate were added over a period of 30 minutes to 30ml. of an aqueous solution containing 3.275 g. of potassium bromide, 0.1 g. of potassium iodide and 1.0 g. of a copolymer of vinyl alcohol (87 mole percent) and vinyl acetate (13 mole percent). The reaction mixture was kept at 70 C. and stirred continuously. After complete addition of the silver nitrate, the reaction mixture was stirred continuously for an additional 30 minutes while the temperature was held at 70 C. The resulting emulsion contained a considerable number of clumps and aggregates. The grains of this emulsion were either spherical or cubical, and the average grain diameter was only 0.19 micron.
• An ammoniacal emulsion was prepared in the following manner. Twenty ml. of an aqueous solution containing 3.82 g. of silver nitrate and an amount of ammonium hydroxide just sutficient to redissolve the precipitate formed initially on addition of ammonium hydroxide to the silver nitrate solution were added with continuous stirring over a period of seconds to 30 ml. of a solution containing 3.14 g. of potassium bromide, 0.1 g. of potassium iodide and 1.0 g. of a copolymer of vinyl alcohol (87 mole percent) and vinyl acetate (13 mole percent). Stirring was continued for an additional 39- minute period. The temperature of the reaction mixture during addition and subsequent stirring was held at 45 C.
• the average grain diameter of the resulting emulsion as determined 20 minutes after beginning of precipitation, was only 0.11 micron. After 40 minutes, the average grain diameter was only 0.15 micron, the mean grain area only 0083 3, and sigma equal to 0.069/L2.
• a neutral emulsion was prepared by the method described in Standard I except that the peptizer used was amylose Nepol Q5-101, A. E. Staley Company. The emulsion obtained was completely unstable.
• ammoniacal emulsion was prepared as described in Standard I except that the peptizer used was amylose.
• the emulsion obtained was unsatisfactory due to very heavy clumping and partial sedimentation.
• STANDARD III A neutral emulsion was prepared as described in Standard I except that cellulose acetate was used as the peptizer. The emulsion obtained was unsatisfactory due to clumping, partial sedimentation and severe inhibition of grain growth.
• Example 1 Poly[methyl(vinyloxymethyl)morpholinium p-toluene sulfonate co-vinyl acetate co-vinyl alcohol] (Molar ratio of the starting copoly(viny1 alcohol-vinyl acetate) to ether amine reactant-121.3. In the following examples, this molar ratio is indicated without any explanation.) Twenty-two grams of a copolymer of vinyl alcohol (87 mole percent) and vinyl acetate (13 mole percent) was placed in a 3-neck, one-liter flask equipped with a mechanical stirrer, a glass stopper and an 8-inch Vigreux column equipped with a take-off still head. A mixture of 87 g.
• a neutral emulsion was prepared with this polymer as described in Standard I.
• the resulting emulsion showed excellent stability and was free from any undesirable clumping, aggregation, or sedimentation effects.
• the emulsion consisted of tabular octahedral grains With average grain diameter equal to 0.85 micron after 40 minutes of ripening (hereinafter defined in terms of the time elapsed since the beginning of precipitation inasmuch as some ripening occurs immediately after some silver halide has been precipitated). The average grain diameter after 60 minutes of ripening was equal to 0.97 micron.
• This polymer was prepared by a method similar to that described for Example 1 with the exception that 74 g. of ethoxymethylmorpholine was used instead of the i-butoxymethyl morpholine.
• a neutral emulsion was prepared with this polymer as described in Standard 1. After 60 minutes of ripening at 70 C., the emulsion was cooled to room temperature and coagulated by addition of 25 cc. saturated sodium sulfate solution. After separation of the coagulum from the supernatant solution by decantation, the coagulum was redispersed by addition of 19.3 ml. water and 16.4 ml. of 11 percent gelatin solution. The resulting emulsion showed excellent stability and was free from any undesirable clumping, agregation, or sedimentation elfects. The grains of this emulsion were tabular octahedra with mean grain area equal to 0.764 and sigma equal to 0.606;?
• This polymer was prepared by the general procedure described for Example 1 with the exception that 50 g. of methoxymethylmorpholine was used in place of the i-butoxymethylmorpholine and 77 g. of methyl p-toluene sulfonate was used for the quaternization.
• a neutral emulsion was prepared with this polymer as described in Standard I. After 60 minutes of ripening at 70 C., the emulsion was cooled to room temperature and coagulated by addition of 25 ml. of saturated sodium sulfate solution. After separation of the coagulum from the supernatant solution by decantation, the coagulum was redispersed by addition of 9.9 ml. of water and 16.1 ml. of an 8.4 percent solution of poly (vinyl alcohol) (Elvanol 7005", E. I. du Pont de Nemours and Company, low molecular weight completely hydrolyzed grade), and stirring at 40 C.
• poly (vinyl alcohol) Elvanol 7005", E. I. du Pont de Nemours and Company, low molecular weight completely hydrolyzed grade
• the resulting emulsion showed excellent stabilty and was free from any undesirable clumping, aggregation or sedimentation effects.
• the grains of this emulsion were tabular octa hedra of average grain diameter equal to 0.85 micron, mean grain area equal to 0878 3, and sigma equal to 0.642,u.
• Example 4 Poly [methyl (vinyloxymethyl )morpholinium p-toluene sulfonate co-vinyl acetate co-vinyl alcohol] This polymer was prepared according to the general procedure described for Example 1 except that in this experiment 35 g. of methoxymethylmorpholine and 55 g. of methyl p-toluene sulfonate were used.
• a neutral emulsion was prepared with this polymer as described in Example 3.
• the emulsion obtained showed excellent stability and was free from any undesrable clumping, aggregation, or sedimentation effects.
• the grains of this emulsion were tabular octahedra with average grain diameter equal to 0.88 micron, mean grain area equal to 0979,1 and sigma equal to 0.690 3.
• Example 5 -Poly [methyl(vinyloxymethyl morpholiniurn p-toluene sulfonate co-vinyl acetate co-vinyl alcohol] (120.46)
• a copolymer of vinyl alcohol (87 mole percent) and vinyl acetate (13 mole percent) (24.6 g.) was mixed with 300 ml. anhydrous dioxane, 300 ml. anhydrous dimethylformamide and 26.2 g. of methoxymethylmorpholine.
• the reacton was run as described for Example 1.
• Sixty grams of methyl p-toluene sulfonate was used for the quaternization.
• the product was purified by dissolving in methanol and precipitating in ether.
• a neutral emulsion was prepared with this polymer by the method described in Standard I.
• the emulsion showed excellent stability and was free from any undesirable clumping, aggregation, or sedimentation effects.
• the grains of this emulsion were tabular octahedra with average grain diameter equal to 0.90 micron after 40 minutes of ripening and 0.96 micron after 60 minutes of ripening.
• Example 6 Poly[methyl(vinyloxymethyl)morphol-inium p-toluene sulfonate co-vinyl acetate co-vinyl alcohol] Prepared as described for Example 1 except in this experiment 20 g. of methoxymethylmorpholine and 32 g. of methyl p-toluene sulfonate were used.
• Example 7 Poly [methyl (vinyloxymethyl morpholinium p-toluene sulfonate co-vinyl acetate co-vinyl alcohol] (110.30)
• a neutral emulsion was prepared with this polymer by the method described in Standard I.
• the emulsion obtained showed excellent stability and was free from any undesirable clumping, aggregation, or sedimentation effects.
• Example 8 Poly [methyl (vinyloxymethyl morpholinium p-toluene sulfonate co-vinyl acetate co-vinyl alcohol] (1:0.23)
• This polymer was prepared by the general method described for Example 5. In this experiment 13 g. of methoxymethylmorpholine was used. An excess (120 g.) of methyl p-toluene sulfonate was used for the quaternization because of rapid gel formation. The final polymer was dissolved in a methanol-water mixture and precipitated in an ether-acetone mixture. An ammoniacal emulsion was prepared with this polymer as described in Example 1. The emulsion obtained showed excellent stability and was free from any undesirable clumping, aggregation, or sedimentation effects. The emulsion consisted of predominantly two size classes: a large size class with grains typically 2 microns in diameter, and a small size class with grains typically 0.2 micron in diameter.
• Example 9 Poly [dipropylmethyl (vinyloxymethyl ammonium p-toluene sulfonate co-vinyl acetate co-vinyl alcohol] (1:1.3)
• Example 1 Twenty-two grams of a copolymer of vinyl alcohol 87 mole percent) and vinyl acetate (13 mole percent), 72.6 g. of methoxyrnethyldipropylamine and 500 ml. of anhydrous dioxane were mixed and reacted according to the method described for Example 1. The product was quaternized with 100 g. of methyl p-toluene sulfonate and isolated as in Example 1.
• a neutral emulsion was prepared as described in Example 3 except for the following dilferences: (1) The peptizer used was the polymer just described, (2) a copolymer of vinyl alcohol (87 mole percent) and vinyl acetate (13 mole percent) was used as the vehicle for the redispersed emulsion grains.
• the emulsion obtained showed excellent stability and was free from any undesirable clumping, aggregation, or sedimentation effects.
• the grains of this emulsion were tabular octahedra with average grain diameter equal to 0.72 micron, mean grain area equal to 0600M, and sigma equal to 0394,1
• average grain diameter was equal to 0.96 micron, the mean grain area equal to 1602 1 and sigma equal to 0.833,.
• Example 10 Morpholinomethylether methyl p-toluene sulfonate of amylose
• Anhydrous amylose (16.2 g., 0.1 mole), 23.2 g. (0.18 mole) of methoxymethylmorpholine and 200 ml. of anhydrous dimethylformamide were stirred together under a stream of N and at for five hours.
• the apparatus consisted of a 3-neck flask equipped with a N inlet tube, a mechanical stirrer and an 8-inch Vigreux column. During the reaction period the methanol reaction product was swept out by the N After cooling the reaction mixture to 25 C., 50 g. of methyl p-toluene sulfonate was added. After 24 hours methanol was added and the yellow polymer precipitated in ether.
• a neutral emulsion was prepared with this polymer by the method described in Standard 1.
• the emulsion obtained showed excellent stability and was free from any undesirable clumping, aggregation, or sedimentation effects.
• the grains of this emulsion were tabular octahedra with average grain diameter equal to 1.0 micron after 40 minutes of ripening and 1.09 micron after 60 minutes of ripening.
• average grain diameter was equal to 0.56 micron after 20 minutes of ripening and 0.68 micron after 40 minutes of ripening.
• Example ll.Morpholinomethyl ether methyl p-toluene sulfate of amylose This polymer was prepared by the method described for Example 10 except 39.3 g. (0.3 mole) of methoxymethylmorpholine and 70 g. of methyl p-toluene sulfonate were used.
• Example 12 Piperidinomethyl ether methyl p-toluene sulfonate of amylose This preparation was identical with Example 10 except 25.8 g. (0.23 mole) of methoxymethylpiperidine was used in place of the corresponding morpholine derivative.
• Example 13 --Dipropylaminomethyl ether methyl p-toluene sulfonate of amylose This preparation was similar to Example 10 except for the use of 43.5 g. (0.3 mole) of methoxymethyldipropylamine instead of the corresponding morpholine derivative.
• Example l4.Di-n-butylaminomethyl ether methyl p-toluene sulfonate of amylose This polymer was prepared by the method used for Example 10 with the exception that 34.6 g. (0.2 mole) of methoxymethyldi-n-butylamine was used in place of the corresponding morpholine derivative.
• Example 15 --Di-n-butylaminomethyl ether methyl p-toluene sulfonate of amylose This preparation was identical to Example 14 except for the quantity of methoxymethyldi-n-butylamine (51.9 g., 0.3 mole) and methyl p-toluene sulfonate (70 g.) used.
• An ammoniacal emulsion was prepared with this polymer as described in Standard I.
• the emulsion obtained showed excellent stability and Was free from any undesirable clumping, aggregation, or sedimentation effects.
• the grains of this emulsion were predominantly cubes with average diameter equal to 0.67 micron after 20 minutes of ripening and 0.75 micron after 40 minutes of ripening.
• Example 16 -Piperidinomethyl ether methyl p-toluene sulfonate of cellulose acetate Anhydrops water soluble cellulose acetate containing 17.6% acetyl (5.1 g.), 3.22 g. of methoxymethylpiperidine and 200 ml. of anhydrous dimethylformamide were mixed in a 300 ml., 3-neck flask equipped with a N inlet tube, a Vigreux column and a mechanical stirrer. This mixture was stirred at 100 C. (oil bath temperature) and a slow stream of N passed through it to sweep out the methanol reaction product. After four hours, the homogeneous solution was cooled to 20 and 8 g. of methyl p-toluene sulfonate added. After 24 hours methanol was added, the solution filtered and poured slowly into ether. The white product was dried in vacuum.
• Example 17 Morpholinomethyl ether methyl p-toluene sulfonate of cellulose acetate any undesirable clumping, aggregation, or sedimentation effects. Most of the grains of this emulsion were cubic. The average grain diameter was equal. to 0.71 micron after 20 minutes of ripening and 0.92 micron after 40 minutes of ripening.
• Emulsions containing the polymers of our invention demonstrate an accelerated rate of physical development over similar emulsions which do not contain such polymers. Further, the polymers employed herein have a blacktoning efifect on the silver obtained by physical development. Increased physical development and black-toning of silver obtained by physical development are highly desirable in various photographic elements and processes, such elements employed in diffusion transfer processes.
• This aspect of our invention is demonstrated in the following examples. In these examples, the polymer employed is a copolymer of vinyl alcohol, vinyl acetate and a vinyloxymethylamine quaternary salt. It has been found that all the other polymers of our invention, described in detail above, also function to increase physical development and as black-toning agents.
• Example 18 illustrates enhanced physical development and black-toning effects in a nucleated silver halide layer which, in addition to gelatin, also contains poly[methyl- (vinyloxymethyl)morpholinium p-toluene sulfonate covinyl acetate co-vinyl alcohol].
• This example demonstrates that (1) silver is formed at a faster rate if the layer contains poly[methyl(vinyloxymethyl)morpholinium p-toluene sulfonate co-vinyl acetate co-vinyl alcohol] in addition to gelatin; and (2) the silver formed by physical development is black-toned.
• Example 18 Initial emulsion The following operations were all carried out under red light. An aqueous solution (20.5 ml.) containing 2.734 g. of silver nitrate and a second aqueous solution (20.5 ml.) containing 2.30 g. of potassium bromide and 0.072 g. of potassium iodide were added simultaneously with continuous stirring to 29.0 ml. of an aqueous solution containing 1.05 g. of gelatin which was kept at a temperature of 45 C. After complete addition of both solutions, stirring at this temperature was continued for an additional six minutes. The emulsion was then removed from the constant temperature bath and cooled to approximately 38 C.
• the pH level of the emulsion was lowered to pH 3 with 1 N sulfuric acid and a sufficient amount of saturated sodium sulfate solution added in order to coagulate the emulsion.
• the coagulum was then chilled and washed repeatedly with cold distilled water by decantation.
• the emulsion was then redispersed by warming, stirring, and addition of sufficient water and dilute sodium hydroxide to bring the emulsion weight to 24.6 g. and the pH level to pH 6.
• the emulsion thus obtained is hereinafter referred to as initial emulsion.
• intermediate emulsion To 12.3 g. initial emulsion there was added 0.8 ml. of water and 19.5 ml. of 9.0 percent aqueous gelatin solution. The resulting emulsion is hereinafter referred to as intermediate emulsion.
• Strips from both coatings which had been shielded from actinic light were then developed (under red light) for different lengths of time in a developer of similar composition as the MO developer, described in Example 3 of US. Patent No. 3,068,097. After completion of the specified development period, the strips were briefly immersed in an acetic acid stop bath and then fixed in Kodak F-24 Fixer in order to remove the nondeveloped silver halide. After the strips had been washed in running tap water and dried, the amount of developed silver (expressed as mg. Ag/ft?) was determined by X-ray spectrometric analysis.
• Example 19 This example illustrates enhanced physical development and toning effects in a nucleated silver halide layer which, in addition to gelatin, also contained one part of poly[methyl(vinyloxymethyl)piperidinium p-toluene sulfonate co-vinyl acetate co-vinyl alcohol] per 99 parts of gelatin.
• This polymer was prepared by the procedure described in Example 2 except 64.6 g. of methoxymethylpiperidine was used instead of the corresponding morpholine derivative.
• the nucleated silver halide coatings were prepared as described in Example 18 except that the above polymer was added to the type 2 coating, and the amounts of gelatin and polymer in this coating were adjusted so as to conform to a 99/1 ratio.
• the coatings were processed in photographic processing solutions as described in Example 18. An estimate of the relative amount of developed silver formed after a given development time in a given strip was then obtained by determining the density at the wave length of maximum absorption (hereinafter referred to as D, A plot of D, max versus development time for the two types of coatings then showed that the rate of formation of physically developed silver was 9.1 times fater if, in addition to gelatin, the coating had also contained the piperidinium polymer. The black toning effect exerted by this polymer was similar to the toning effect of the corresponding morpholinium polymer described in Example 18.
• Example 20 This example illustrates enhanced physical development and toning effects in a nucleated silver halide layer which, in addition to gelatin, also contained one part of poly di-n-butylmethyl vinyloxymethyl ammonium p-toluene sulfonate co-vinyl acetate co-vinyl alcohol] per 99 parts of gelatin.
• This polymer was prepared in accordance with the procedure described in Example 3 except 86.5 g. of methoxymethyldi-n-butylarnine was used instead of the corresponding morpholine derivative.
• Example 18 The procedure used was the same as in Example 18 except that the above polymer was used in the type 2 coating. A plot of D, max versus development time for the two types of coatings then showed that the rate of formation of physically developed silver was 2.3 times faster if, in addition to gelatin, the coating had also contained the ammonium polymer. The black toning effect exerted by this latter polymer was similar to the toning effect of the morpholinium polymer described in Example 18.
• Example i 2 1 This example illustrates the increased amount of silver which can be transferred in the course of a silver halide diffusion transfer process from a silver halide layer to a nucleated receiving layer when, in addition to gelatin, poly[methyl(vinyloxymethyl)morpholinium p-toluene sulfonate co-vinyl acetate co-vinyl alcohol] is also incorporated into the silver halide layer.
• poly[methyl(vinyloxymethyl)morpholinium p-toluene sulfonate co-vinyl acetate co-vinyl alcohol] is also incorporated into the silver halide layer.
• the increased rate of solution of the silver halide grains in the silver halide layer which is brought about by the presence of this polymer then provides for a 'more readily available supply of silver ions which then diffuse from the silver halide layer into the receiving layer.
• Receiving layers were prepared in the following manner: To 25 ml. of 2.0 percent aqueous gelatin solution there was added 1.25 ml. of a suspension of silver nuclei containing 1.0 g. silver nucleinate/liter, 0.4 ml. of 5 percent aqueous saponin solution, and 0.5 ml. of aqueous 0.314 percent formaldehyde solution. This solution was coated on Reflection Print Support with a coating knife (clearance equal to 0.003 inch) and dried.
• the receiving layer was immersed for 20 seconds into a developer of the following composition (all quantities are expressed as g./liter):
• Silver halide layer contained a 4/1 Contact time contained only mixture of gelatin (seconds) gelatin as a and the polymer of vehicle Example 1 as the vehicle 14
• Example 22 This example illustrates the increased amount of silver which can be transferred in the course of a silver halide diffusion process from a silver halide layer to a nucleated receiving layer, if this receiving layer contains not only gelatin but also poly[methyl(vinyloxymethyl)morpholinium p-toluene sulfonate co-vinyl acetate co-vinyl alcohol].
• This same example also illustrates black-toning effects which are achieved by incorporation of the polymer into the receiving layer.
• the two types of receiving layers were prepared as follows: 25 ml. of coating solution containing either 5 percent gelatin, for the preparation of receiving layers containing only gelatin as the vehicle, or 4 percent gelatin and 1 percent poly[methyl(vinyloxymethyl)morpholinium p-toluene .sulfonate co-vinyl acetate co-vinyl alcohol] (prepared as described in Example 1) for the preparation of receiving layers containing a 4/1 ratio of gelatin and the morpholinium polymer, 3.2 ml. of a suspension of silver nuclei (1.0 g. silver nucleinate/liter), 0.4 ml. of 5 percent aqueous saponin solution, and 0.2 ml. of 0.314 percent formaldehyde solution were coated on Reflection Print Support by means of a coating knife (clearance equal to 0.003 inch) and dried.
• a strip of (unexposed) Kodak fine grain positive film was immersed for 3 seconds in the developer described in Example 21 and then pressed against the nucleated receiving layer for .a specified contact time. After separation of the two layers, the receiving layer was dried. The amount of silver which had transferred into this layer was then determined by X-ray spectrometric analysis.
• Emulsions prepared in accordance with our invention, and emulsions containing the polymers employed herein, may have incorporated therein chemical and optical sensitizers, speed increasing compounds, gelatin plasticizers and hardeners, stabilizers, coating aids and the like emulsion addenda such as described in Beavers US. Patent 3,039,873, col. 10 through col. 12.
• the emulsion may be used in various applications, such as those described in col. 12 and 13 of the above Beavers patent.
• the emulsions may be coated on any suitable support, such as cel lulose acetate, polyester, polycarbonate, paper and polyolefin coated paper.
• R and R each represent a substituent selected from the group consisting of alkyl radicals having from 1 to 8 carbon atoms, aryl radicals; and R and R taken together, represent the atoms necessary to complete a heterocyclic ring composed of to 6 atoms;
• R represents an alkyl radical having from 1 to 6 carbon atoms;
• R represents an alkylene radical having from 1 to 5 carbon atoms; and,
• A represents an acid anion, and (B) polysaccharides containing repeating units having the following general formula:
• l 1 represents the repeating unit of the polysaccharide; and R R R R and A have the same meaning given above; said polymers and polysaccharides having a ratio of total repeating units to repeating units having the specified general formula of less than 5:1.
• polysaccharide is a far hydrolized, water-soluble cellulose acetate containing from 13 to 26% acetyl.
• R and R each represent a substituent selected from the group consisting of alkyl radicals having from 1 to 8 carbon atoms; aryl radicals, and, R and R taken together, represent the atoms necessary to complete a heterocyclic ring composed of 5 to 6 atoms; R represents an alkyl radical having from 1 to 6 carbon atoms;
• A represents an acid anion, said copolymer having a ratio of total repeating units to repeating units having the above formula of from 4:1 to 1:1.
• R and R each represent a substituent selected from the group consisting of alkyl radicals having from 1 to 8 carbon atoms; aryl radical, and, R and R taken together, represent the atoms necessary to complete a heterocyclic ring composed of 5 to 6 atoms;
• R represents an alkyl radical having from 1 to 6 carbon atoms;
• R represents an alkylene radical having from 1 to 5 carbon atoms; and,
• A represents an acid anion;
• l I represents the repeating unit of 1 7 the polysaccharide; and R R R R and A have the same meaning given above; said polymers and polysaccharides having a ratio of total repeating units to repeating units having the specified general formula of less than :1.
• the dispersion of claim 10 wherein the polysaccharide is a far hydrolyzed, water soluble cellulose acetate containing from 13 to 26% acetyl.
• R and R each represent a substituent selected from the group consisting of alkyl radicals having from 1 to 8 carbon atoms; aryl radicals, and, R and R taken together, represent the atoms necessary to complete a heterocyclic ring composed of 5 to 6 atoms; R represents an alkyl radical having from 1 to 6 carbon atoms; and, A represents an acid anion, said copolymer having a ratio of total repeating units to repeating units having the above formula of from 4:1 to 1:1.
• a dispersion of silver halide in an aqueous solution of copoly[methyl(vinyloxymethyl)morpholinium ptoluene sulfonate-vinylalcohol-vinyl acetate] which contains less than about vinyl acetate and has a ratio of total repeating units to the morpholinium sulfonate containing units of from 4:1 to 1:1.
• a photographic silver halide emulsion having incorporated therein, in an amount sufiicient to effectively enhance physical development of the silver halide, a hydrophilic polymer having a plurality of quaternary nitrogen atoms each chemically bonded by an ether linkage to the polymer with the oxygen of said ether linkage bonded directly to a carbon atom in the polymer chain.
• R and R each represent a substituent selected from the group consisting of alkyl radicals having from 1 to 8 carbon atoms; aryl radicals, and, R and R taken together, represent the atoms necessary to complete a heterocyclic ring composed of 5 to 6 atoms;
• R represents an alkyl radical having from 1 to 6 carbon atoms;
• R represents an alkylene radical having from 1 to 5 carbon atoms; and,
• A represents an acid anion;
• I represents the repeating unit of the polysaccharide; and R R R R and A have the same meaning given above; said polymers and polysaccharides having a ratio of total repeating units to repeating units having the specified general formula of less than 5:1.
• a photographic silver halide emulsion having incorporated therein, in an amount sufficient to effectively enhance physical development of the silver halide, a hydrophilic copolymer essentially consisting of vinyl alcohol repeating units and repeating units having the following general formula:
• R and R each represent a substituent selected from the group consisting of alkyl radicals having from 1 to 8 carbon atoms; aryl radicals, and, R and R taken together, represent the atoms necessary to complete a heterocyclic ring composed of 5 to 6 atoms; R, represents an alkyl radical having from 1 to 6 carbon atoms; and, A represents an acid anion, saidl copolymer having a ratio of total repeating units to repeating units having the above formula of from 4:1 to 1:1.
• a reception element adapted for use in a silver halide diffusion transfer process comprising a suppont having coated thereon, in an amount sufiicient to effectively enhance the amount of silver deposited on the support, a hydrophilic polymer having a plurality of quaternary nitrogen atoms each chemically bonded by an ether linkage to the polymer with the oxygen of said ether linkage bonded directly to a carbon atom in the polymer chain.

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• 1965
  • 1965-04-15 US US448266A patent/US3425836A/en not_active Expired - Lifetime
• 1966
  • 1966-03-10 DE DE19661595569 patent/DE1595569B2/de active Pending
  • 1966-03-28 BE BE678582D patent/BE678582A/xx unknown
  • 1966-04-13 DE DE19661547678 patent/DE1547678A1/de active Pending
  • 1966-04-15 GB GB16510/66A patent/GB1139446A/en not_active Expired
  • 1966-04-15 GB GB16509/66A patent/GB1148482A/en not_active Expired
  • 1966-04-15 GB GB35567/68A patent/GB1148483A/en not_active Expired

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