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
  • G03C8/42—Structural details
  • G03C8/52—Bases or auxiliary layers; Substances therefor
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
  • C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
  • C08B37/0006—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid
  • C08B37/0024—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid beta-D-Glucans; (beta-1,3)-D-Glucans, e.g. paramylon, coriolan, sclerotan, pachyman, callose, scleroglucan, schizophyllan, laminaran, lentinan or curdlan; (beta-1,6)-D-Glucans, e.g. pustulan; (beta-1,4)-D-Glucans; (beta-1,3)(beta-1,4)-D-Glucans, e.g. lichenan; Derivatives thereof
  • C08B37/0027—2-Acetamido-2-deoxy-beta-glucans; Derivatives thereof
  • C08B37/003—Chitin, i.e. 2-acetamido-2-deoxy-(beta-1,4)-D-glucan or N-acetyl-beta-1,4-D-glucosamine; Chitosan, i.e. deacetylated product of chitin or (beta-1,4)-D-glucosamine; Derivatives thereof
• • 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
  • C08F8/48—Isomerisation; Cyclisation
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
  • C08J5/18—Manufacture of films or sheets

Definitions

• the present invention is especially related to silver and color diffusion transfer processes of the type wherein a transfer image is obtained in a single step by treating an exposed photosensitive element with a layer of a suitable processing solution to provide, as a function of development, an imagewise distribution of image-forming components, and transferring the imagewise distribution of image-forming components through the layer of processing solution to a superposed image-receiving element to form a transfer image thereon.
• an exposed photosensitive silver halide emulsion is developed and almost concurrently therewith a soluble silver complex is obtained by reaction of a silver halide solvent with the unexposed and undeveloped silver halide of said emulsion.
• the photosensitive silver halide emulsion is wet with a layer of processing composition which is spread between a photosensitive element comprising the silver halide emulsion and a print-receiving element.
• the processing composition effects development of the latent image in the emulsion and substantially contemporaneous therewith forms a soluble silver complex, for example, a thiosulfate or thiocyanate, with undeveloped silver halide.
• This soluble silver complex is, at least in part, transported in the direction of the35ceiving element and the silver thereof is largely precipitated thereon to form a positive transfer image.
• dye developers i.e., compounds which contain in the same molecule both the chromophon'c system of a dye and also a silver halide developing function
• dye developers i.e., compounds which contain in the same molecule both the chromophon'c system of a dye and also a silver halide developing function
• a layer of the processing solution is applied between the photosensitive element and a superposed image-receiving element, and the imagewise distribution of image-forming components is transferred through the layer of processing solution to the imagereceiving layer.
• the processing solution comprises a film-forming, viscosity-increasing reagent, such, for example, as hydroxyethyl cellulose or sodium carboxymethyl cellulose to facilitate the spreading ice of the solution, between the photosensitive element and the image-receiving element.
• a film-forming, viscosity-increasing reagent such, for example, as hydroxyethyl cellulose or sodium carboxymethyl cellulose to facilitate the spreading ice of the solution, between the photosensitive element and the image-receiving element.
• the image-forming components remaining in the film of processing solution may be used to enhance the density of the transfer image by having the film of processing solution preferably adhere to the image-receiving element when it is separated from the photosensitive element.
• the present invention is concerned with providing means for substantially cutting down the time which the layer of processing solution takes to set on the image-receiving element. It is particularly useful when it is employed with imagereceiving elements which have means therein for reducing the alkalinity of the processing solution, such as disclosed in the copending application of Edwin H. Land, Ser. No. 234,864, filed Nov. 1, 1962.
• One object of the present invention is to provide in diffusion transfer processes means for accelerating the setting times of layers of processing solution which are interspersed between a photosensitive element and an image-receiving element during processing and which are adapted to preferentially adhere to the image-receiving element when said elements are separated.
• Another object of the present invention is to provide processing solutions for diffusion transfer processes comprising means therein for accelerating the setting time of said processing solution.
• the invention accordingly comprises the process involving the several steps and the relation and order 'of one or more of such steps with respect to each of the others, and the product possessing the features, properties and the relation of elements which are exemplified in the following detailed disclosure, and the'scope of the application of which will be indicated in the claims.
• the setting time of the film of processing solution on imagereceiving elements, and especially on image-receiving elements having means therein for reducing the alkalinity of the processing solution may be substantially reduced by incorporating in the processing solution a polymeric substance which is soluble in strongly alkaline solutions, e.g., solutions having pHs greater than 11.0, and particularly a pH between 12 and 14, but is insoluble and precipitates out when the pHs reduced to 7 to 11.0 and, more preferably, 9 to 11.
• a polymeric substance which is soluble in strongly alkaline solutions, e.g., solutions having pHs greater than 11.0, and particularly a pH between 12 and 14, but is insoluble and precipitates out when the pHs reduced to 7 to 11.0 and, more preferably, 9 to 11.
• the preferred polymeric materials for use in the present invention are those which, in addition to possessing the above solubility characteristics, are (1) stable in the strongly alkaline processing solutions for long periods of time, (2) are compatible with the other reagents present and (3) form clear films with the film forming viscosityincreasing reagents which may be present.
• Polymeric materials which are particularly useful in the present invention are the weakly ionized polymeric acids, e.g., acids having ionization constants between about 10- and 10- and, more preferably, between 10" and 10
• Preferred groups of compounds within this class are the polyphenols, i.e., polymers comprising a plurality of hydroxyphenyl groups therein.
• aromatic hydroxy groups are slightly ionized and are Weak acids.
• materials of this type are phenolformaldehyde condensation polymers such as the resols or novolaks.
• Other examples of such polyphenolic polymers are the hydroxybenzaldehyde acetals of a hydroxy substituted linear polymer e.g., polyvinyl alcohol, i.e.,
• acetals of this type are those formed with the hydrolysis product of a copolymer of vinyl acetate and a-trifiuoromethyl vinyl acetate.
• Such hydrolysis products may be represented as possessing segments of the following structure:
• the preferred hydroxybenzaldehydes for forming the above acetals are those in which the hydroxy group is meta to the aldehyde group. Such meta compounds provide acetals which have especially good stability in the strongly alkaline processing solutions.
• Another class of weakly ionized polymeric acids for use in the present invention are the primary and secondary polysulfonamides, i.e., polymers comprising a plurality of SO NH and/ or -SO NHR radicals wherein R may be an alkyl or phenyl group.
• Materials of this type which have been found particularly useful are polymers comprising phenyl sulfonamide groups.
• polymers condensation polymers of benzenesulfonamide and formaldehyde such as Santolite MHP (trademark of Monsanto Chemical Co).
• condensation polymers of benzenesulfonamide and formaldehyde such as Santolite MHP (trademark of Monsanto Chemical Co).
• linear polysulfonarnides such as those formed from benzene disulfonyl chloride and a diamine such as hexamethylene diamine.
• weakly ionized polymeric acids which have been found useful in the present invention are polymers comprising ot-trifluoromethylvinyl alcohol segments (hydroxyl group is weakly ionized), and benzene sulfonamides of deacetylated chitin, such as formed by condensing benzene sulfonyl chloride with deacetylated chitin.
• Still another group of materials which are useful in the present invention are polymeric substances which are soluble in strong alkaline solutions, e.g., pH greater than 11 but become hydrogen bonded and are insoluble in solutions having pHs between about 7 to 9 and, more preferably, 9 to 11.
• strong alkaline solutions e.g., pH greater than 11 but become hydrogen bonded and are insoluble in solutions having pHs between about 7 to 9 and, more preferably, 9 to 11.
• polyhydroxymethylene i.e., polyhydroxymethylene
• OH OH which may be prepared by hydrolyzing polyvinylene carbonate.
• Another example of such a material is poly- 2,2-bis-hydroxymethylethylene.
• the present invention is especially useful with image-receiving elements wherein means are provided therein for reducing the alkalinity of the proc essing solution.
• such means may comprise incorporating an acid such, for example, as oxalic, phthalic, benzoic, etc., in the image-receiving layer itself or in adjacent layers in which it may be available to neutralize alkali in the processing solution.
• an acid-reacting layer is disposed in the imagereceiving element.
• the acid-reacting layer generally comprises a polymeric acid having non-diffusing acid groups thereon, e.g., cellulose acetate hydrogen phthalate, or a partial ester of an ethylene/maleic acid copolymer.
• a polymeric acid having non-diffusing acid groups thereon e.g., cellulose acetate hydrogen phthalate, or a partial ester of an ethylene/maleic acid copolymer.
• the alkali subsequent to transfer of the imageforming substances, migrates into such layers and is neutralized, thereby reducing the pH of the layer of processing solution.
• the acid layer is separated from the image-receiving layer by a neutral layer or admixed with other neutral polymers to prevent premature reduction of the alkali concentration before development.
• the present invention is primarily intended for use in processes wherein the layer of processing solution is adapted, when spread between the photosensitive element and the image-receiving element, to preferentially adhere to the image-receiving element when the elements are separated.
• the layer of the image-receiving element which is contiguous to the layer of processing solution, has a greater affinity for the layer of processing solution than the contiguous layer of the photosensitive element.
• preferential adhesion will vary depending upon the film forming material incorporated in the processing solution. Generally, it can be readily determined and achieved by simple procedures and technique known to the art.
• precipitating nuclei e. g., metallic sulfides such, for example, as lead sulfide, cadmium sulfide, zinc sulfide and nickel sulfide, and metallic selenides such as lead selenide and zinc selenide, in the image-receiving layer to facilitate the formation of the silver image thereon.
• precipitating nuclei may be dispersed directly in the processing solution, as disclosed in US. Patent No. 2,662,822.
• a dye mordant may be included in the processing solution in color transfer processes.
• Example 1 122 gms. (1.0 mole) m-hydroxybenzaldehyde was dissolved in 1200 ml. of acetic acid in a three-necked, round bottomed flask equipped with a stirrer and condenser. 132 gms. (3.0 moles) of Elvanol 70-60 (substantially completely hydrolyzed polyvinyl alcohol), and 1 ml. of phosphoric acid were added and the mixture was heated over a steam bath for about four hours until a clear dark-brown solution resulted. 1.5 gms. sodium acetate were added and the contents of the flask was decanted into water. The acetal of polyvinyl alcohol and m-hydroxybenzaldehyde which precipitated out was washed twice with water and dried under vacuum.
• Example 2 14.0 gms. of polyvinyl alcohol was dissolved with heat and stirring in 400 ml. glacial acetic acid. 19.6 gms. of p-formyl benzenesulfonamide and 2 ml. of 85% phosphoric acid was added to the hot solution and the mixture was heated, with stirring, on a steam bath overnight. The resulting acetal of polyvinyl alcohol and p-formyl benzenesulfonamide was Washed in acetone and dried under vacuum.
• Example 3 Vinylene carbonate comprising 0.4% by weight, of azo-bis-isobutyronitrile was polymerized in bulk, under vacuum, at 70 C. for 72 hours. The resulting polymer was dissolved in dimethylformainide and precipitated into methanol and dried under vacuum. gms. of the polymer was dissolved in 100 cc. of 5% aqueous sodium hydroxide solution with stirring and heating at 40 C. Heating was continued for about 20 minutes until the polymer precipitated out. The mixture was cooled and neutralized with acetic acid to complete the precipitation. The resulting polyhydroxy-methylene was washed with water and dried.
• Example 4 Part A.-A copolymer of vinyl acetate and a-trifluoromethylvinylacetate was prepared by polymerizing in bulk, under ultraviolet light, 15.4 gms. (0.1 mole) 2-acetoxy-3,3,3-trifiuoropropene and 8.6 gms. (0.1 mole) of vinyl acetate.
• the resulting polymer was purified by precipitation from acetone into hexane and dried. 17 gms. of the resulting polymer was hydrolyzed at reflux in methyl alcohol having therein a catalytic amount of sodium methoxide. The resulting hydrolyzed polymer was precipitated through the addition of acetic acid and then washed and dried.
• Part B The dried polymer was dissolved in 50 cc. of acetic acid. 12.2 gms. (0.1 mole) of 3-hydroxybenzaldehyde and 1 cc. of 85% phosphoric acid was added and the mixture was stirred for four hours at 60 C. The resulting partial acetal of 3-hydroxybenzaldehyde and the vinyl alcohol-a-trifluoromethylvinyl alcohol copolyrner was precipitated into water, washed until neutral and dried.
• Example 5 100 gms. of polyacrolein was dispersed with stirring in 2650 ml. of pyridine and 2250 ml. of 40% formaldehyde. The mixture was heated to 70 C. and 500 ml. of 2 N sodium hydroxide was slowly added and the solid dissolved. Heating is continued overnight at 70 C. and the solution is filtered and precipitated into acetone. The precipitated poly-2,Z-bis-hydroxymethyl-ethylene was triturated twice with ethanol, once with a 3 to 1 acetonewater mixture and then hardened with acetone.
• Example 6 92.4 gms. (1.14 m.) 37% formaldehyde was condensed with 130 gms. (1.38 m.) freshly distilled phenol in the presence of 2 gm. oxalic acid dihydrate. The resulting novolaktic phenol-formaldehyde polymer was precipitated from an acetone-methanol solution into water and dried under vacuum.
• Example 7 10 gms. deacetylated chitin was dissolved in 1000 cc. of water and cc. of concentrated hydrocloric acid. The solution was made just alkaline with 9% sodium hydroxide and then 50 cc. in excess of the 90% sodium hydroxide solution was added. 10 cc. of benzensulfonyl chloride was added dropwise With rapid stirring and the resulting mixture was neutralized with sodium hydroxide. The resulting benzene-sulfonated chitin was filtered oil, washed with water and stirred for three hours in 10% aqueous hydrochloric acid. After being filtered and washed, the polymer was precipitated from dilute sodium hydroxide with hydrochloric acid and washed and dried.
• a multilayer color negative such as disclosed in U.S. Patent No. 2,983,606.
• such negatives comprise a support bearing in turn a gelatin layer having dispersed therein, in a water-immiscible solvent, a cyan dye developer such as 1,4-bis-[amethyl ,8 hydroquino'nyl ethylamino] 5,8, dihydroxy-anthraquinone; a red-sensitive silver iodobromide emulsion layer; a gelatin interlaye'r; a gelatin layer having dispersed therein, in a water-immiscible solvent, a magenta dye developer such as 2-[p-(2',5'-dihydroxyphenethyl)-phenylazo]-4-isopropoxyl-naphthol; a green-sensitive silver iodobromide emulsion layer; a gelatin interlayer; a gelatin
• yellow dye developer such as lphenyl 3 N n hexylcarbamyl 4 [.p (2',5' dihydroxyphene'thyl) phenylazo] 5 pyrazolone; a bluesensitive silver iodobr'oinide emulsion layer and an outer thin stripping layer of cellulose acetate hydrogen phthalate so that the processing solution will preferentially adhere to the image-receiving element.
• Example 8 (control) Water cc Potassium hydroxide 1 gm 11.2 Hydroxyethyl cellulose grn 3.9 Benzotriazole gm 3.0 N-benzyl-a-p-icolinium bromide gm 2.0 Potassium thiosulfa'te gm 0.4 Lithium nitrate gm 0.2
• the image-receiving element was spread between said image-receiving element and said exposed multicolor negative as they were brought into superposed relationship. After an imbibition period of 1% minutes the image-receiving element was separated from the negative. Upon separation, the layer of processing solution having a multicolor image therein, preferentially adhered to the imagereceiving element and intensified the color image thereon. The layer of processing solution set so that it could not be moved around by the finger using normal handling pressure after about 3 minutes.
• Example 9 The procedure of Example 8 was repeated except that the processing solution contained only 3.0 gms. of the hydroxyethyl cellulose and additionally 1.5 gms. of an acetal of polyvinyl alcohol and m-hydroxybenzaldehyde, as prepared in Example 1. Upon separating the image-receiving element from the negative, the layer of processing solution set so that it could not be moved around by the finger using normal handling pressure after about 1% minutes.
• Example 10 The procedure of Example 9 was repeated except that 1.5 gms. of an acetyl of polyvinyl alcohol and p-formylbenzenesulfonamide, as prepared in Example 2, was used in place of the acetal of polyvinyl alcohol and m-hydroxybenzaldehyde. Upon separation, the layer of processing solution set so that it could not be moved around by the finger using normal handling pressure after about 1% minutes.
• Example 11 The procedure of Example 9 was repeated except that 1.0 gm. of polyhydroxymethylene, as prepared in Example 3, was used in place of theacetal of polyvinyl alcohol and m-hydroxybenzaldehyde. Upon separation the layer of processing solution set so that it could not be moved around with the finger using normal. handling pres sure after about 2 minutes.
• Example 12 The procedure of Example 9 was repeated except that 1.0 gm. of an a-trifluoromethylvinyl alcohol-vinyl alcohol copolymer, as prepared in Example 4 (part A), was used in place of the acetal of polyvinyl alcohol and m-hydroxybenzaldehyde. Upon separation the layer of processing solution set so that it could not be moved around with the finger using normal handling pressure after about 2 minutes.
• Example 14 The procedure of Example 9 was repeated except that 1.5 grns. of a novolaktic phenol-formaldehyde resin, as prepared in Example 6, was used in place of the acetal of polyvinyl alcohol and rn-hydroxybenzaldehyde. Upon separation, the layer of processing solution set so that it could not be moved with the finger using normal handling pressure after about 1 minute and 35 seconds.
• Example 15 The procedure of Example 9 was repeated except that 1.5 gms. of an acetyl of polyvinyl alcohol and p-hydroxybenzaldehyde was used in place of the acetal of polyvinyl alcohol and m-hydroxybenzaldehyde. Upon separation, the layer of processing solution set so that it could not be moved with the finger using normal handling pressure after about 2 minutes.
• Example 16 The procedure of Example 9 was repeated using 1.5 grns. of Santolite MHP (trade name of Monsanto Chemical Co. for a formaldehydebenzenesul-fonamide condensation polymer) in place of the acetal polyvinyl alcohol and m-hydroxybenzaldehyde. Upon separation, the layer of processing solution set so that it could not be moved with the finger using normal handling pressure after about 1 minute and 30 seconds.
• Santolite MHP trade name of Monsanto Chemical Co. for a formaldehydebenzenesul-fonamide condensation polymer
• Example 17 The procedure of Example 9 was repeated except that 1.5 gms. of benzenesulfonated chitin, as prepared in Example 7, was used in place of the acetal of polyvinyl alcohol and m-hydroxybenzaldehyde.
• the layer of processing solution set so that it could not be moved with the finger using normal handling pressure after about 1 minute and 30 seconds.
• Example 18 The procedure of Example 9 was repeated except that 1.5 grns. of poly-a,a-bis-(hydroxymethyl)-ethylene, as prepared in Example 5, was used in place of the acetal.
• the layer of processing solution set so that it could not be moved with the finger using normal handling pressure after about 1 minute and 20 seconds.
• Example 19 The procedure of Example 9 was repeated except that in place of the acetal polyvinyl alcohol and rn-hydroxybenzaldehyde there was used 1.5 gms. of a mixed acetal formed by reacting 1 mol. of polyvinyl alcohol with 0.33 mol. of trifluoroacetaldehyde and 0.33 mol. of m-hydroxybenzaldehyde in the presence of a catalytic amount of phosphoric acid.
• the layer of processing solution set so that it could not be moved with the finger using normal handling pressure after about 1 minute and 15 seconds.
• Example 20 The procedure of Example 9 was repeated except that in place of the acetal of polyvinyl alcohol and m-hydroxybenzaldehyde there was used 1.5 gins. of mixed acetal formed by condensing 2 mol. of polyvinyl alcohol with 0.33 mol. of 3-hydroxybenzaldehyde and 0.33 mol. of 4-pyridine-carboxaldehyde in the presence of a catalytic amount of 85% phosphoric acid.
• the layer of processing solution set so that it could not be moved with a finger using normal handling pressure after about 1 minute and 30 seconds.
• Example 21 The procedure of Example 9 was repeated except that only 2.0 gins. of the hydroxyethylcellulose was employed and in place of the hydroxybenzaldehyde acetal there was used 2.0 gms. of a linear sulfonamide prepared by condensing about equal molar amounts of hexamethylene diamine and 1,3-benzene disulfonyl chloride in the presence of sodium carbonate. The layer of processing solution set in about 1 minute on the image-receiving element.
• Example 22 The procedure of Example 9 was repeated except that in place of the hydroxybenzaldehyde acetal there was employed 1.5 guns. of an acetal formed by condensing 5.35 grns. of a copolyrner of vinyl alcohol and u-trifluoromethyl-vinyl alcohol, as prepared in Example 4, part A, with 6.36 gins. of p-formylbenzene sulfonamide.
• the layer of processing solution set in about 1 /2 minutes on the image-receiving element.
• the pH of the processing solution which was greater than 13 initially, was reduced to at least about 9 to 11 at about the time the negative is separated, e.g., about 1 minute and 30 seconds. Usually it will continue to drop so that it will be, for example, between about 7 to 9 in about 1 minute after the negative is separated. In some instances the pH has dropped to values as low as 6 or even lower within several minutes after imbibition was terminated.
• this invention has been described in terms of a separate image-receiving or image-carrying element to which the processing solution preferentially adheres, it may also be used in diffusion transfer processes employing only a single sheet, i.e., a viscous processing composition containing a film-forming polymer is applied to a photosensitive element, e.g., by a doctor blade or other coating techniques, and a transfer image is formed in the solidified layer of said processing composition which is allowed to remain adhered to the photosensitive element.
• the developed negative image may be masked by a layer of white pigment, e.g., titanium dioxide. Processes of this type are disclosed, e.g., in the aforementioned U.S. Patent No. 2,662,822.
• a process as defined in claim 1 wherein said polymeric substance is a polymeric acid having an ionization constant between about 10 and 10 4.
• a process as defined in claim 3 wherein said polymeric acid has an ionization constant between about 10'" and 10 5.
• a process as defined in claim 3 wherein said polymeric acid is a polyphenolic polymer.
• polyphenolic polymer is an acetal of a hydroxybenzaldehyde and a hydroXy-substituted linear polymer.
• polymeric acid is selected from the group consisting of primary and secondary polysulfonamides.
• polysulfonamide is an acetal of a primary formalbenzene sulfonarnide and a hydroxy-substituted linear polymer.
• polymeric acid is a polymer comprising ot-trifluoromethylvinyl alcohol segments.
• polymeric substance is benzenesulfonamide of deacetylated chitin.
• polymeric substance is a polymeric acid having an ionization constant between about 10' and 10- 17.
• polymeric acid has an ionization constant between about 10- and 10*.
• polyphenolic polymer is an acetal of a hydroxybenzaldehyde and a hydroxy-substituted linear polymer.
• polymeric acid is selected from the group consisting of primary and secondary polysulfonamides.
• polysulfonamide is an acetal of a primary formylbenzene sulfonamide and a hydroxy-substituted linear polymer.
• polymeric acid is a polymer comprising a-trifiuoromethylvinyl alcohol segments.

Landscapes

• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• Organic Chemistry (AREA)
• Polymers & Plastics (AREA)
• Medicinal Chemistry (AREA)
• Engineering & Computer Science (AREA)
• Life Sciences & Earth Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• General Physics & Mathematics (AREA)
• Molecular Biology (AREA)
• Biochemistry (AREA)
• Materials Engineering (AREA)
• General Health & Medical Sciences (AREA)
• Physics & Mathematics (AREA)
• Structural Engineering (AREA)
• Architecture (AREA)
• General Chemical & Material Sciences (AREA)
• Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
• Photosensitive Polymer And Photoresist Processing (AREA)

Priority Applications (7)

Applications Claiming Priority (1)

Publications (1)

Family

ID=23916765

Family Applications (1)

Country Status (4)

Cited By (4)

Families Citing this family (2)

Citations (4)

• 1965
  • 1965-08-25 US US482620A patent/US3362822A/en not_active Expired - Lifetime
• 1966
  • 1966-08-23 DE DE1572005A patent/DE1572005C3/de not_active Expired
  • 1966-08-23 GB GB37745/66A patent/GB1159985A/en not_active Expired
  • 1966-08-25 BE BE685973D patent/BE685973A/xx not_active IP Right Cessation

Patent Citations (4)

Also Published As

Similar Documents