US2522771A - Photographic silver halide emulsions - Google Patents
Photographic silver halide emulsions Download PDFInfo
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- US2522771A US2522771A US561826A US56182644A US2522771A US 2522771 A US2522771 A US 2522771A US 561826 A US561826 A US 561826A US 56182644 A US56182644 A US 56182644A US 2522771 A US2522771 A US 2522771A
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- Prior art keywords
- water
- polyvinyl alcohol
- gel
- silver halide
- light
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 239000000839 emulsion Substances 0.000 title claims description 31
- -1 silver halide Chemical class 0.000 title claims description 25
- 229910052709 silver Inorganic materials 0.000 title claims description 21
- 239000004332 silver Substances 0.000 title claims description 21
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 36
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 33
- 238000000034 method Methods 0.000 claims description 17
- 239000000203 mixture Substances 0.000 claims description 17
- 239000000084 colloidal system Substances 0.000 claims description 16
- 239000007864 aqueous solution Substances 0.000 claims description 15
- 239000000463 material Substances 0.000 claims description 14
- 239000000047 product Substances 0.000 claims description 11
- 239000006185 dispersion Substances 0.000 claims description 10
- 150000003839 salts Chemical class 0.000 claims description 10
- 239000003349 gelling agent Substances 0.000 claims description 7
- 238000001704 evaporation Methods 0.000 claims description 5
- 235000018102 proteins Nutrition 0.000 claims description 5
- 108090000623 proteins and genes Proteins 0.000 claims description 5
- 102000004169 proteins and genes Human genes 0.000 claims description 5
- 230000001235 sensitizing effect Effects 0.000 claims description 5
- 230000008961 swelling Effects 0.000 claims description 5
- 150000001371 alpha-amino acids Chemical class 0.000 claims description 4
- 235000008206 alpha-amino acids Nutrition 0.000 claims description 4
- 239000007859 condensation product Substances 0.000 claims description 2
- XLYOFNOQVPJJNP-PWCQTSIFSA-N Tritiated water Chemical compound [3H]O[3H] XLYOFNOQVPJJNP-PWCQTSIFSA-N 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 33
- 239000000499 gel Substances 0.000 description 31
- 239000008273 gelatin Substances 0.000 description 27
- 229920000159 gelatin Polymers 0.000 description 27
- 239000000243 solution Substances 0.000 description 27
- 108010010803 Gelatin Proteins 0.000 description 24
- 235000019322 gelatine Nutrition 0.000 description 24
- 235000011852 gelatine desserts Nutrition 0.000 description 24
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 24
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 12
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 12
- 230000001681 protective effect Effects 0.000 description 9
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 229920002554 vinyl polymer Polymers 0.000 description 7
- 238000001879 gelation Methods 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 229920002689 polyvinyl acetate Polymers 0.000 description 6
- 239000011118 polyvinyl acetate Substances 0.000 description 6
- 229910001961 silver nitrate Inorganic materials 0.000 description 6
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 5
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 4
- 239000007857 degradation product Substances 0.000 description 4
- 238000011161 development Methods 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 230000017854 proteolysis Effects 0.000 description 4
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 3
- 239000002639 bone cement Substances 0.000 description 3
- 229920002678 cellulose Polymers 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 230000003678 scratch resistant effect Effects 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- 239000004471 Glycine Substances 0.000 description 2
- 241000282320 Panthera leo Species 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 229910001508 alkali metal halide Inorganic materials 0.000 description 2
- 150000008045 alkali metal halides Chemical class 0.000 description 2
- 239000005018 casein Substances 0.000 description 2
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 2
- 235000021240 caseins Nutrition 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000012937 correction Methods 0.000 description 2
- 239000003292 glue Substances 0.000 description 2
- 239000005337 ground glass Substances 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 229920001290 polyvinyl ester Polymers 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- HMUNWXXNJPVALC-UHFFFAOYSA-N 1-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical group C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C(CN1CC2=C(CC1)NN=N2)=O HMUNWXXNJPVALC-UHFFFAOYSA-N 0.000 description 1
- 102000009027 Albumins Human genes 0.000 description 1
- 108010088751 Albumins Proteins 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 1
- 108010076119 Caseins Proteins 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 238000005903 acid hydrolysis reaction Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000005904 alkaline hydrolysis reaction Methods 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000003609 aryl vinyl group Chemical group 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N butyric aldehyde Natural products CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 150000008049 diazo compounds Chemical class 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- GFJVXXWOPWLRNU-UHFFFAOYSA-N ethenyl formate Chemical compound C=COC=O GFJVXXWOPWLRNU-UHFFFAOYSA-N 0.000 description 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 159000000014 iron salts Chemical class 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001289 polyvinyl ether Polymers 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- NBBJYMSMWIIQGU-UHFFFAOYSA-N propionic aldehyde Natural products CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 150000003378 silver Chemical class 0.000 description 1
- GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 238000005406 washing Methods 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
- 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
Definitions
- This invention relates to photographic silver halide emulsions which comprise a silver halide dispersed in a thermal-reversible gel composed of a polyvinyl alcohol which is mixed with a gelling amount of a water-soluble nitrogenous substance, such as water-soluble proteins, protein degradation products, and alpha-amino acids.
- thermal-reversible gel we have reference to a gel which on heating becomes liquid and on cooling again becomes a gel.
- polyvinyl alcohol we include not only polyvinyl alcohol polymers, but other polymeric vinyl compounds which contain hydroxy groups, such as partially hydrolyzed polyvinyl acetate, polyvinyl propionate, polyvinyl butyrate, polyvinyl propionaldehyde acetals, polyvinyl butyral- ,dehyde acetals, and polyvinyl ethers, such as polymers of alkyl and aryl vinyl ethers.
- any water-soluble polyvinyl alcohol can be converted into a thermal-reversible gel suitable as a carrier or protective colloid for lightsensitive silver salts.
- the protective colloid in which the light-sensitive silver halide grains are suspended must keep the grains of silver halide finely dispersed in the emulsion in order to eliminate clumping and eventual graininess in the photographic image.
- the colloid must also be stable over a long period of time so that both the undeveloped and the processed emulsion are of good permanence.
- the protective colloid must not impart photographic characteristics to the light-sensitive particles which are undesirable.
- the carrier must be such that it can be simply handled and yet be accurately reproduced so that the emulsions can be prepared and applied in the form of coatings in practical methods. Another important requirement of the colloid is that it must permit the penetration of treating solutions without adversely affecting its strength, toughness and permanence.
- Gelatin has universally been used as a protective colloid for light-sensitive silver halides in such emulsions because it satisfies most of the abovementioned requirements.
- gelatin has certain disadvantages which it has long been sought to overcome. Being a natural product, one of its most serious drawbacks is the variation inthe properties of different batches. Thus, a batch of gelatin obtained from one locality will differ in properties from that obtained in another.
- gelatin is susceptible to the action of bacteria. In order to obtain the highly purified gelatin required for photographic purposes, there is necessitated expensive and numerous refining procedures.
- polyvinyl esters polyvinyl acetate, partially hydrolyzed cellulose esters, regenerated cellulose, water-soluble polyamides, cellulose nitrate and polyvinyl alcohol,.alone, or in combination with other substances.
- Another object of our invention is to provide a photographic emulsion which contains a substance capable of duplication and possessing standardized properties which may be used as a protective colloid for the silver halide salts in place of gelatin.
- a still further object of our invention is to provide a carrier for silver halide photographic emulsions which serves as a substitute for gelatin and is capable of modification to give emulsions having a wider range of physical properties than is possible withgelatin.
- the photographic emulsions of our invention may be prepared by merely adding to an aqueous solution of a polyvinyl alcohol, aqueous solutions of alkali metal halides conventionally used for producing the light-sensitive silver salt and silver nitrate. To this mixture may be then added a gelling amount of the water-soluble nitrogenous compound which is to be used as the gelling agent. In an alternative procedure, the alkali metal halides are added to a solution of polyvinyl alcohol and this mixture is then removed to a dark room where there is added a solution of silver nitrate containing a small amount of the water-soluble nitrogenous com pound.
- the emulsion thus formed is dried. On adding Water it swells to form a gel from which the soluble salts are washed out. This gel may then be melted and the viscous melt formed is then coated on any suitable support, such as glass, paper, or films made of cellulose derivatives.
- Example 1 To parts by weight of a 10% aqueous solution of far-hydrolyzed polyvinyl acetate havin a viscosity of centipoises in 4% solution was added one part of glycine. This mixture was then heated to boiling for a few minutes, and spread out to dry at a temperature ranging from about 2060 C. The dried material, although insoluble in cold water, swells therein to form a tough gel which is thermal-reversible. Upon warming, the gel melts and may be coated on glass or other supports to form, after drying, a clear colorless, tough film, which is especially scratch-resistant.
- Example 2 8.5 parts by Weight of a far-hydrolyzed polyvinyl acetate of medium viscosity and 1.5 parts of gelatin were dissolved in 80 parts of hot water and the solution spread out to dry at room temperature.
- the dried material although insoluble in cold water, swells therein to form a tough gel which is thermal-reversible.
- This gel may be washed in cool water for long periods of time without dissolving.
- the washed gel is thermal-reversible and may be melted and cast to form a colorless, tough, scratch-resistant film on drying.
- the dried film is completely trans parent and homogeneous. When more than 20% of gelatin was added, however, the resulting dried films are no longer transparent, but resemble coarse ground glass in appearance. Mixtures of such concentrations are not compatible.
- Example 3 1 part by weight of bone glue was added to 9 parts of the 10% solution of polyvinyl alcohol described in Example 1. The mixture was heated for a few minutes until the glue had dissolved and the solution spread out to dry at room temperature. Although insoluble in cold water, the dried material swells therein to form a gel. This gel is also thermal-reversible.
- Example 4 To 55 cc. of a 14% aqueous solution of a medium viscosit polyvinyl alcohol (containing less than 5% by weight of acetate calculated as vinyl acetate) was added a solution of 5 grams of potassium bromide and 0.3 gram of potassium iodide dissolved in 15 cc of water. The mixture was then removed to a dark room and to it was added, over a period of two minutes with vigorous stirring, a solution of 5 grams of silver nitrate dissolved in 15 cc. of a 10% gelatin solution. The emulsion is spread out to dry at room temperature. The dried material is then swollen in cool water to form a gel from which the water-soluble salts are washed out. This gel was then melted on a water bath and coated on glass, paper, and cellulose derivative supports. Upon exposure and development by the usual photographic procedures, images of good quality were produced.
- a medium viscosit polyvinyl alcohol containing less than 5% by weight of acetate calculated
- Example 5 In 15 cc. of a 3% gelatin solution there is added 15 cc. of an aqueous solution containing 5 grams of potassium bromide and 0.3 gram of potassium iodide. To this mixture is then added a solution of 5 grams of silver nitrate dissolved in 15 cc. of water to precipitate the silver halide. To this is then added 55 cc. of a 20% aqueous solution of medium viscosity polyvinyl alcohol (containing less than 5% by weight of acetate calculated as vinyl acetate), and the mixture vigorously stirred. The mixture is then spread out to dry at room temperature. The dried material is swollen in cool water to form a gel from which the water-soluble salts are washed out. This gel is then melted by heating and coated on a transparent cellulosic film. Upon exposure and development by the usual photographic procedures, images of good quality were produced.
- Example 6 The same procedure was followed as in Example 4, except that an equivalent amount of .bone glue was substituted for the gelatin.
- the emulsion so obtained when coated, exposed, and processed gave fine quality images.
- the coating was found to be somewhat more sticky than in that of Example 4.
- Example 7 cc. of a 10% solution of polyvinyl alcohol of medium viscosity (as in Example 4) is diluted with cc. of water. The following solutions are then run in with rapid stirring through the time of addition:
- Example 8 3 grams of the dried polvinyl alcohol-gelatin product obtained according to Example 2 is swollen and dissolved by heating at about 50 C. in 80 cc. of water. To this solution is added a solution of 5 grams of potassium bromide and 0.3 gram of potassium iodide in 20 cc. of water. The solution is cooled to about 40 C. and with vigorous stirring a solution of 5 grams of silver nitrate in cc. of water is added. 15 grams of the dried polyvinyl alcohol-gelatin product which is swollen With water is then added. The emulsion is then spread out to dry and the dried material is then swollen in cold water and the soluble salts removed therefrom. After melting by heating, the viscous liquid obtained is coated on a suitable support, and permitted to chill set.
- Example 9 The procedure is the same as in Example 8 but instead of starting with the dried polyvinyl alcohol-gelatin product, one starts with a solution containing 2.6 grams of polyvinyl alcohol and 0.5 gram of gelatin dissolved in 80 cc. of water.
- the nitrogenous gelling agents are required and, infact, larger amounts are, as a rule, incompatible with the polyvinyl alcohol and give films which resemble coarse ground glass in appearance. While these incompatible mixtures might be useful for some purposes, especially when the added substance is dispersed in the polyvinyl alcohol solution, we prefer to utilize those compositions which are compatible and form transparent films on drying.
- the amount of water-soluble nitrogenous substances which is added to the polyvinyl alcohol solution need only be suflicient to cause gelling. In general, the amount added may range from about 1% to about based on the weight of the polyvinyl alcohol, where transparent films are to be obtained. Where opaque films are desired, the amount may vary from.
- the exact physical properties of the photographic emulsion, made according to our process, may be varied to some extent, not only by the nature and the amount of the added nitrogenous substance, but also by varying the molecular weight, degree of hydrolysis, and nature of the other substituents of the polyvinyl alcohol employed. If, for example, a polyvinyl acetate of high molecular weight is hydrolyzed as, for example, according to the process of the Skirrow Patent No. 1,971,951, to yield a polyvinyl alcohol, solutions containing this product will be more viscous than those of equal concentration containing a polyvinyl alcoho1 prepared from a lower molecular weight polyvinyl acetate. In this case, a smaller proportion of the gelation agent is employed than in the case when a polyvinyl alcohol of lower molecular weight is employed as the protective colloid.
- the degree of hydrolysis of the polyvinyl ester also contributes to the physical properties of the polyvinyl alcohol formed and, therefore, is an important factor in determining the characteristics of the aqueous solutions and the gels obtained therefrom. Also playing a part in the gelling characteristics of the solution of the protective colloid is the nature of the unhydrolyzed groups. Thus, for example, if a polymer of vinyl formate is partially hydrolyzed to produce a polydiffer from those of a similar product made from a polymer of vinyl acetate.
- the formyl groups have a greater tendency to exert attractive forces of the so-called secondary valence type on one another, thereby increasing the tendency to gel and'the strength of the resulting gel due to the improved cohesive properties present in such a polymen p
- Other substituted groups may be present in the polyvinyl alcohol molecule.
- such polyvinyl alcohols fall within the scope of this invention which are produced by hydrolyzing an interpolymer of a vinyl ester with other vinyl compounds, such as nitriles, esters, amides and similar derivatives of acrylic and alpha-substituted acrylic acids, as well as the free acids themselves.
- Thewater-soluble protein degradation products which we use as gelation agents may be produced in any well known manner, as for example, according to the processes set forth in United States Patents Nos. 1,719,711,.1,727,866, and 1,815,983, that is, by either acid or alkaline hydrolysis.
- photosensitive substances in addition to the silver halides, other photosensitive substances, well known in the photographic art, may be employed, as for example, chromates, iron salts, diazo compounds, and the like.
- our invention provides photographic emulsions which have out.- standing advantages over emulsions containing gelatin and the like. Thus, they may be prepared with definite purity and standardized properties which can be reproduced at all times, as contrasted with gelatin emulsions whose properties may vary in marked degree due to the differences that exist in difierent batches of the gelatin.
- a method of preparing a light-sensitive photographic emulsion in the form of a thermalreversible gel, suitable for sensitizing photographic materials and adapted to form a film of tough, transparent colloid having a light-sensitive silver halide dispersed therein which consists in preparing a dispersion of a light-sensitive silver halide in an aqueous solution of a polyvinyl alcohol which contains, as the sole gelling agent therefor, a gelling amount from about 1% to about 20% by weight f the amount of polyvinyl alcohol, of a water-soluble nitrogenous compound selected from the group consisting of proteins, protein degradation products, alpha-amino acids and their condensation products, evaporating the resulting dispersion to dryness and swelling the dried composition thus obtained in cold water, whereby thep-roduot is converted to a gel and any water-soluble salts contained therein are washed out.
- a method of preparing a light-sensitive photographic emulsion in the form of a thermalreversi-ble gel, suitable for sensitizing photographic materials and adapted to form a film of tough, transparent colloid having a light-sensitive silver halide dispersed therein which consists in preparing a dispersion of a light-sensitive silver halide in an aqueous solution of a polyvinyl alcohol which contains, as the sole gelling agent therefor, a gelling amount of from about 1% to about 20% by weight of the amount of weight of polyvinyl alcohol of gelatin, evaporating the resulting dispersion to dryness, and swelling the dried composition thus obtained in cold water, whereb the product is converted to a gel and any water-soluvinyl 1 1, th properties of thi product 111 ble salts contained therein are washed out.
- a method of preparing a light-sensitive photographic emulsion in the form of a thermalreversible gel, suitable for sensitizing photographic materials and adapted to form a film of tough, transparent colloid having a light-sensitive silver halide dispersed therein which consists in preparing a dispersion of a light-sensitive silver halide in an aqueous solution of a polyvinyl alcohol which contains, as the sole gelling agent therefor, a gelling amount of from about 1% to about 20% by weight of the amount by weight of polyvinyl alcohol, of bone glue, evaporating the resulting dispersion to dryness, and swelling the dried composition thus obtained in cold water, whereby the product is converted to a gel and any water-soluble salts contained therein are washed out.
- a method of preparing a light-sensitive photographic emulsion in the form of a thermalreversible gel, suitable for sensitizing photo-- graphic materials nd adapted to form a film of tough, transparent colloid having a light-sensitive silver halide dispersed therein which consists in preparing a dispersion of a light-sensitive silver halide in an aqueous solution of a polyvinyl alcohol Which contains, as the sole gelling agent therefor, a gelling amount of from about 1% to about 20% by weight of the amount of weight of polyvinyl alcohol, of glycine, evaporating the resulting dispersion to dryness, and swelling the REFERENCES CITED
- the following references are of record in the file of this patent:
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- General Physics & Mathematics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
Patented Sept. 19, 1950 PHOTOGRAPHIC SILVER HALIDE EMULSIONS Carl E. Barnes, Belvidere, N. J and William 0. Ney, Jr., Easton, Pa., assignors to General Aniline & Film Corporation, New York, N. Y., a corporation of Delaware No Drawing. Application November 3, 1944, Serial No. 561,826
8 Claims.
This invention relates to photographic silver halide emulsions which comprise a silver halide dispersed in a thermal-reversible gel composed of a polyvinyl alcohol which is mixed with a gelling amount of a water-soluble nitrogenous substance, such as water-soluble proteins, protein degradation products, and alpha-amino acids.
By the terms thermal-reversible gel we have reference to a gel which on heating becomes liquid and on cooling again becomes a gel. By the term polyvinyl alcohol we include not only polyvinyl alcohol polymers, but other polymeric vinyl compounds which contain hydroxy groups, such as partially hydrolyzed polyvinyl acetate, polyvinyl propionate, polyvinyl butyrate, polyvinyl propionaldehyde acetals, polyvinyl butyral- ,dehyde acetals, and polyvinyl ethers, such as polymers of alkyl and aryl vinyl ethers. By our process any water-soluble polyvinyl alcohol can be converted into a thermal-reversible gel suitable as a carrier or protective colloid for lightsensitive silver salts.
The protective colloid in which the light-sensitive silver halide grains are suspended must keep the grains of silver halide finely dispersed in the emulsion in order to eliminate clumping and eventual graininess in the photographic image. The colloid must also be stable over a long period of time so that both the undeveloped and the processed emulsion are of good permanence. Likewise, the protective colloid must not impart photographic characteristics to the light-sensitive particles which are undesirable. In addition, the carrier must be such that it can be simply handled and yet be accurately reproduced so that the emulsions can be prepared and applied in the form of coatings in practical methods. Another important requirement of the colloid is that it must permit the penetration of treating solutions without adversely affecting its strength, toughness and permanence.
Gelatin has universally been used as a protective colloid for light-sensitive silver halides in such emulsions because it satisfies most of the abovementioned requirements. However, gelatin has certain disadvantages which it has long been sought to overcome. Being a natural product, one of its most serious drawbacks is the variation inthe properties of different batches. Thus, a batch of gelatin obtained from one locality will differ in properties from that obtained in another. Moreover, gelatin is susceptible to the action of bacteria. In order to obtain the highly purified gelatin required for photographic purposes, there is necessitated expensive and numerous refining procedures.
The desirability of a synthetic material which possesses the advantageous properties of gelatin and which can be exactly reproduced so that a material of predetermined and standardized properties, without differences in different batches, is always obtained has long been recognized and a gelatin substitute has long been sought by photographic manufacturers. Among the many substitutes proposed, however, none has apparently met the requirements for a pro tective colloid for practical photographic emulsion manufacture. Extensive research for the development of emulsion media better than gelatin has as yet failed to. produce a satisfactory substitute. Among the materials which have been sug ested for this purpose are partially hydrolyzed polyvinyl esters, polyvinyl acetate, partially hydrolyzed cellulose esters, regenerated cellulose, water-soluble polyamides, cellulose nitrate and polyvinyl alcohol,.alone, or in combination with other substances.
An important practical disadvantage of polyvinyl alcohol as a direct substitute for gelatin in photographic emulsions is the failure of its aqueous solutions to exhibit the phenomenon of thermal-reversible gelation. This property is one of great importance in the manufacture of photographic emulsions, since it makes possible the removal of soluble salts by washing in cold water and also permits coating of the emulsion on the support by simply heating the gel until it melts to a liquid. It is for this reason that various substances have been added to polyvinyl alcohol to impart the property of thermal-reversible gelation. i
It is an object of our invention to provide a photographic emulsion which contains a protective colloid possessing the property of thermalreversible gelation in aqueous solution and which may be used as a substitute for gelatin.
Another object of our invention is to provide a photographic emulsion which contains a substance capable of duplication and possessing standardized properties which may be used as a protective colloid for the silver halide salts in place of gelatin.
A still further object of our invention is to provide a carrier for silver halide photographic emulsions which serves as a substitute for gelatin and is capable of modification to give emulsions having a wider range of physical properties than is possible withgelatin.
We have ,discovered'that water-soluble proteins and protein degradation products, such as casein, albumin, gelatin and glue, as well as certain alpha-amino acids and their condensation 3 products, such as diketopiperazines, when added to aqueous solutions of polyvinyl alcohols impart the property of thermal-reversible gelation.
The photographic emulsions of our invention may be prepared by merely adding to an aqueous solution of a polyvinyl alcohol, aqueous solutions of alkali metal halides conventionally used for producing the light-sensitive silver salt and silver nitrate. To this mixture may be then added a gelling amount of the water-soluble nitrogenous compound which is to be used as the gelling agent. In an alternative procedure, the alkali metal halides are added to a solution of polyvinyl alcohol and this mixture is then removed to a dark room where there is added a solution of silver nitrate containing a small amount of the water-soluble nitrogenous com pound.
The emulsion thus formed is dried. On adding Water it swells to form a gel from which the soluble salts are washed out. This gel may then be melted and the viscous melt formed is then coated on any suitable support, such as glass, paper, or films made of cellulose derivatives.
On drying, a tough film, which is. especially scratch-resistant, is formed. Upon exposure and development by the usual photographic technique, images of good quality are produced.
The following examples are illustrative of our invention:
Example 1 To parts by weight of a 10% aqueous solution of far-hydrolyzed polyvinyl acetate havin a viscosity of centipoises in 4% solution was added one part of glycine. This mixture was then heated to boiling for a few minutes, and spread out to dry at a temperature ranging from about 2060 C. The dried material, although insoluble in cold water, swells therein to form a tough gel which is thermal-reversible. Upon warming, the gel melts and may be coated on glass or other supports to form, after drying, a clear colorless, tough film, which is especially scratch-resistant.
Example 2 8.5 parts by Weight of a far-hydrolyzed polyvinyl acetate of medium viscosity and 1.5 parts of gelatin were dissolved in 80 parts of hot water and the solution spread out to dry at room temperature. The dried material, although insoluble in cold water, swells therein to form a tough gel which is thermal-reversible. This gel may be washed in cool water for long periods of time without dissolving. The washed gel is thermal-reversible and may be melted and cast to form a colorless, tough, scratch-resistant film on drying. The dried film is completely trans parent and homogeneous. When more than 20% of gelatin was added, however, the resulting dried films are no longer transparent, but resemble coarse ground glass in appearance. Mixtures of such concentrations are not compatible.
Example 3 1 part by weight of bone glue was added to 9 parts of the 10% solution of polyvinyl alcohol described in Example 1. The mixture was heated for a few minutes until the glue had dissolved and the solution spread out to dry at room temperature. Although insoluble in cold water, the dried material swells therein to form a gel. This gel is also thermal-reversible.
4 Example 4 To 55 cc. of a 14% aqueous solution of a medium viscosit polyvinyl alcohol (containing less than 5% by weight of acetate calculated as vinyl acetate) was added a solution of 5 grams of potassium bromide and 0.3 gram of potassium iodide dissolved in 15 cc of water. The mixture was then removed to a dark room and to it was added, over a period of two minutes with vigorous stirring, a solution of 5 grams of silver nitrate dissolved in 15 cc. of a 10% gelatin solution. The emulsion is spread out to dry at room temperature. The dried material is then swollen in cool water to form a gel from which the water-soluble salts are washed out. This gel was then melted on a water bath and coated on glass, paper, and cellulose derivative supports. Upon exposure and development by the usual photographic procedures, images of good quality were produced.
Example 5 In 15 cc. of a 3% gelatin solution there is added 15 cc. of an aqueous solution containing 5 grams of potassium bromide and 0.3 gram of potassium iodide. To this mixture is then added a solution of 5 grams of silver nitrate dissolved in 15 cc. of water to precipitate the silver halide. To this is then added 55 cc. of a 20% aqueous solution of medium viscosity polyvinyl alcohol (containing less than 5% by weight of acetate calculated as vinyl acetate), and the mixture vigorously stirred. The mixture is then spread out to dry at room temperature. The dried material is swollen in cool water to form a gel from which the water-soluble salts are washed out. This gel is then melted by heating and coated on a transparent cellulosic film. Upon exposure and development by the usual photographic procedures, images of good quality were produced.
Example 6 The same procedure was followed as in Example 4, except that an equivalent amount of .bone glue was substituted for the gelatin. The emulsion so obtained when coated, exposed, and processed gave fine quality images. The coating was found to be somewhat more sticky than in that of Example 4.
Example 7 cc. of a 10% solution of polyvinyl alcohol of medium viscosity (as in Example 4) is diluted with cc. of water. The following solutions are then run in with rapid stirring through the time of addition:
40 cc. of a 50% solution of silver nitrate 12.8 grams of potassium bromide,
3 grams of potassium chloride,
0.5 gram of potassium iodide, and
40 cc. of water.
200 cc. of a 10% solution of polyvinyl alcohol is then added and the emulsion stirred until well mixed, at a temperature of 40 C. There is then added 16 cc. of a 10% gelatin solution. The resulting mixture is then spread out to dry at room temperature. The dried material is then swollen in cool water to form a gel from which the water-soluble salts are washed out. This gel is then melted and coated, the same as set forth in Example 4.
Example 8 3 :grams of the dried polvinyl alcohol-gelatin product obtained according to Example 2 is swollen and dissolved by heating at about 50 C. in 80 cc. of water. To this solution is added a solution of 5 grams of potassium bromide and 0.3 gram of potassium iodide in 20 cc. of water. The solution is cooled to about 40 C. and with vigorous stirring a solution of 5 grams of silver nitrate in cc. of water is added. 15 grams of the dried polyvinyl alcohol-gelatin product which is swollen With water is then added. The emulsion is then spread out to dry and the dried material is then swollen in cold water and the soluble salts removed therefrom. After melting by heating, the viscous liquid obtained is coated on a suitable support, and permitted to chill set.
Example 9 The procedure is the same as in Example 8 but instead of starting with the dried polyvinyl alcohol-gelatin product, one starts with a solution containing 2.6 grams of polyvinyl alcohol and 0.5 gram of gelatin dissolved in 80 cc. of water.
In general, only small amounts of the nitrogenous gelling agents are required and, infact, larger amounts are, as a rule, incompatible with the polyvinyl alcohol and give films which resemble coarse ground glass in appearance. While these incompatible mixtures might be useful for some purposes, especially when the added substance is dispersed in the polyvinyl alcohol solution, we prefer to utilize those compositions which are compatible and form transparent films on drying. The amount of water-soluble nitrogenous substances which is added to the polyvinyl alcohol solution need only be suflicient to cause gelling. In general, the amount added may range from about 1% to about based on the weight of the polyvinyl alcohol, where transparent films are to be obtained. Where opaque films are desired, the amount may vary from.
above 20% to about 98%. Heating facilitates solution of the ingredients in the mixture.
The exact physical properties of the photographic emulsion, made according to our process, may be varied to some extent, not only by the nature and the amount of the added nitrogenous substance, but also by varying the molecular weight, degree of hydrolysis, and nature of the other substituents of the polyvinyl alcohol employed. If, for example, a polyvinyl acetate of high molecular weight is hydrolyzed as, for example, according to the process of the Skirrow Patent No. 1,971,951, to yield a polyvinyl alcohol, solutions containing this product will be more viscous than those of equal concentration containing a polyvinyl alcoho1 prepared from a lower molecular weight polyvinyl acetate. In this case, a smaller proportion of the gelation agent is employed than in the case when a polyvinyl alcohol of lower molecular weight is employed as the protective colloid.
The degree of hydrolysis of the polyvinyl ester also contributes to the physical properties of the polyvinyl alcohol formed and, therefore, is an important factor in determining the characteristics of the aqueous solutions and the gels obtained therefrom. Also playing a part in the gelling characteristics of the solution of the protective colloid is the nature of the unhydrolyzed groups. Thus, for example, if a polymer of vinyl formate is partially hydrolyzed to produce a polydiffer from those of a similar product made from a polymer of vinyl acetate. The formyl groups have a greater tendency to exert attractive forces of the so-called secondary valence type on one another, thereby increasing the tendency to gel and'the strength of the resulting gel due to the improved cohesive properties present in such a polymen p Other substituted groups may be present in the polyvinyl alcohol molecule. Thus, such polyvinyl alcohols fall within the scope of this invention which are produced by hydrolyzing an interpolymer of a vinyl ester with other vinyl compounds, such as nitriles, esters, amides and similar derivatives of acrylic and alpha-substituted acrylic acids, as well as the free acids themselves.
Thewater-soluble protein degradation products which we use as gelation agents may be produced in any well known manner, as for example, according to the processes set forth in United States Patents Nos. 1,719,711,.1,727,866, and 1,815,983, that is, by either acid or alkaline hydrolysis.
In addition to the silver halides, other photosensitive substances, well known in the photographic art, may be employed, as for example, chromates, iron salts, diazo compounds, and the like.
. It will thus be seenthat our invention provides photographic emulsions which have out.- standing advantages over emulsions containing gelatin and the like. Thus, they may be prepared with definite purity and standardized properties which can be reproduced at all times, as contrasted with gelatin emulsions whose properties may vary in marked degree due to the differences that exist in difierent batches of the gelatin.
We claim:
1. A method of preparing a light-sensitive photographic emulsion in the form of a thermalreversible gel, suitable for sensitizing photographic materials and adapted to form a film of tough, transparent colloid having a light-sensitive silver halide dispersed therein, which consists in preparing a dispersion of a light-sensitive silver halide in an aqueous solution of a polyvinyl alcohol which contains, as the sole gelling agent therefor, a gelling amount from about 1% to about 20% by weight f the amount of polyvinyl alcohol, of a water-soluble nitrogenous compound selected from the group consisting of proteins, protein degradation products, alpha-amino acids and their condensation products, evaporating the resulting dispersion to dryness and swelling the dried composition thus obtained in cold water, whereby thep-roduot is converted to a gel and any water-soluble salts contained therein are washed out.
2. A method of preparing a light-sensitive photographic emulsion in the form of a thermalreversi-ble gel, suitable for sensitizing photographic materials and adapted to form a film of tough, transparent colloid having a light-sensitive silver halide dispersed therein, which consists in preparing a dispersion of a light-sensitive silver halide in an aqueous solution of a polyvinyl alcohol which contains, as the sole gelling agent therefor, a gelling amount of from about 1% to about 20% by weight of the amount of weight of polyvinyl alcohol of gelatin, evaporating the resulting dispersion to dryness, and swelling the dried composition thus obtained in cold water, whereb the product is converted to a gel and any water-soluvinyl 1 1, th properties of thi product 111 ble salts contained therein are washed out.
3. A method of preparing a light-sensitive photographic emulsion in the form of a thermalreversible gel, suitable for sensitizing photographic materials and adapted to form a film of tough, transparent colloid having a light-sensitive silver halide dispersed therein, which consists in preparing a dispersion of a light-sensitive silver halide in an aqueous solution of a polyvinyl alcohol which contains, as the sole gelling agent therefor, a gelling amount of from about 1% to about 20% by weight of the amount by weight of polyvinyl alcohol, of bone glue, evaporating the resulting dispersion to dryness, and swelling the dried composition thus obtained in cold water, whereby the product is converted to a gel and any water-soluble salts contained therein are washed out.
4. A method of preparing a light-sensitive photographic emulsion in the form of a thermalreversible gel, suitable for sensitizing photo-- graphic materials nd adapted to form a film of tough, transparent colloid having a light-sensitive silver halide dispersed therein, which consists in preparing a dispersion of a light-sensitive silver halide in an aqueous solution of a polyvinyl alcohol Which contains, as the sole gelling agent therefor, a gelling amount of from about 1% to about 20% by weight of the amount of weight of polyvinyl alcohol, of glycine, evaporating the resulting dispersion to dryness, and swelling the REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 2,006,002 Schneider June 25, 1935 2,127,621 Staud et al. Aug. 23, 1938 2,174,629 Greiner Oct, 3, 1939 2,184,310 Meigs et al. Dec. 26, 1939 2,249,537 McDowell et a1 July 15, 1941 2,276,323 Lowe Mar. 17, 1942 2,311,059 Lowe Feb. 16, 1943 2,376,371 LoWe et a1 May 22, 1945 Certificate of (Correction Patent No. 2,522,771 September 19, 1950 CARL E. BARNES ET AL.
It is hereby certified that error appears in the printed specification of the above numbered patent requirlng correction as follows:
Column 6, line 7 O, andcolumn 7 line 28, for the Word of second occurrence, read by; column 6, line 71, after alcohol lnsert a comma;
and that the said Letters Patent should be read as corrected above, so that the same may conform to the record of the casein the Patent Ofiice. Signed and sealed this 13th day of February, A. D. 1951.
THOMAS F. MURPHY,
Assistant Commissioner of Patents.
Claims (1)
1. A METHOD OF PREPARING A LIGHT-SENSITIVE PHOTOGRAPHIC EMULSION IN THE FORM OF A THERMALREVERSIBLE GEL, SUITABLE FOR SENSITIZING PHOTOGRAPHIC MATERIALS AND ADAPTED TO FORM A FILM OF TOUGH, TRANSPARENT COLLOID HAVING A LIGHT-SENSITIVE SILVER HALIDE DISPERSED THEREIN, WHICH CONSISTS IN PREPARING A DISPERSION OF A LIGHT-SENSITIVE SILVER HALIDE IN AN AQUEOUS SOLUTION OF A POLYVINYL ALCOHOL WHICH CONTAINS, AS THE SOLE GELLING AGENT THEREFOR, A GELLING AMOUNT FROM ABOUT 1% TO ABOUT 20% BY WEIGHT OF THE AMOUNT OF POLYVINYL ALCOHOL, OF A WATER-SOLUBLE NITROGENOUS COMPOUND SELECTED FROM THE GROUP CONSISTING OF PROTEINS, PROTEIN DEGRATION PRODUCTS, ALPHA-AMINO ACIDS AND THEIR CONDENSATION PRODUCTS, EVAPORATING THE RESULTING DISPERSION TO DRYNESS AND SWELLING THE DRIED COMPOSITION THUS OBTAINED IN COLD WATER, WHEREBY THE PRODUCT IS CONVERTED TO A GEL AND ANY WATER-SOLUBLE SALTS CONTAINED THEREIN ARE WASHED OUT.
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| US561826A US2522771A (en) | 1944-11-03 | 1944-11-03 | Photographic silver halide emulsions |
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| Application Number | Priority Date | Filing Date | Title |
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| US561826A US2522771A (en) | 1944-11-03 | 1944-11-03 | Photographic silver halide emulsions |
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Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US2687958A (en) * | 1949-05-14 | 1954-08-31 | Azoplate Corp | Light-sensitive layers for the printing industry |
| US2746863A (en) * | 1954-02-10 | 1956-05-22 | Gen Aniline & Film Corp | Light sensitive diazotype material |
| US2822272A (en) * | 1954-02-10 | 1958-02-04 | Gen Aniline & Film Corp | Light sensitive diazotype material |
| US2829053A (en) * | 1954-11-08 | 1958-04-01 | Du Pont | Copolymers and photographic emulsions containing the same |
| US2968558A (en) * | 1954-12-08 | 1961-01-17 | Eastman Kodak Co | Thermo-reversible gels and photographic emulsions prepared therewith |
| US3038870A (en) * | 1956-12-27 | 1962-06-12 | Du Pont | Process of preparing and extruding an aqueous gel of polytetrafluoroethylene |
| US3140950A (en) * | 1962-05-21 | 1964-07-14 | Harold J Brunk | Blueprint paper and coating composition including polyvinyl alcohol for making same |
| US3431109A (en) * | 1964-10-16 | 1969-03-04 | Addressograph Multigraph | Heat sensitive diazotype materials |
| US3778270A (en) * | 1970-11-12 | 1973-12-11 | Du Pont | Photosensitive bis-diazonium salt compositions and elements |
| US3847614A (en) * | 1971-09-13 | 1974-11-12 | Scott Paper Co | Diazo photopolymer composition and article comprising carboxylated resin |
| US3867154A (en) * | 1973-07-23 | 1975-02-18 | Keuffel & Esser Co | Desalination of silver halide photographic emulsions utilizing sulfated polyvinyl alcohol |
| US4433043A (en) * | 1980-11-18 | 1984-02-21 | Toppan Printing Co., Ltd. | Water based photosensitive composition with hydrolyzate of mammal collagen |
| US5432245A (en) * | 1990-04-02 | 1995-07-11 | Eastman Kodak Company | Method of coating thermoreversible heat-thickening polyacrylamides |
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| US2006002A (en) * | 1932-11-29 | 1935-06-25 | Agfa Ansco Corp | Manufacture of photographic silver halide emulsion layers |
| US2127621A (en) * | 1936-04-16 | 1938-08-23 | Eastman Kodak Co | Photographic emulsions |
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| US2006002A (en) * | 1932-11-29 | 1935-06-25 | Agfa Ansco Corp | Manufacture of photographic silver halide emulsion layers |
| US2174629A (en) * | 1934-09-15 | 1939-10-03 | Anton F Greiner | Process for printing and photographing and material therefor |
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Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2687958A (en) * | 1949-05-14 | 1954-08-31 | Azoplate Corp | Light-sensitive layers for the printing industry |
| US2746863A (en) * | 1954-02-10 | 1956-05-22 | Gen Aniline & Film Corp | Light sensitive diazotype material |
| US2822272A (en) * | 1954-02-10 | 1958-02-04 | Gen Aniline & Film Corp | Light sensitive diazotype material |
| US2829053A (en) * | 1954-11-08 | 1958-04-01 | Du Pont | Copolymers and photographic emulsions containing the same |
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| US3038870A (en) * | 1956-12-27 | 1962-06-12 | Du Pont | Process of preparing and extruding an aqueous gel of polytetrafluoroethylene |
| US3140950A (en) * | 1962-05-21 | 1964-07-14 | Harold J Brunk | Blueprint paper and coating composition including polyvinyl alcohol for making same |
| US3431109A (en) * | 1964-10-16 | 1969-03-04 | Addressograph Multigraph | Heat sensitive diazotype materials |
| US3778270A (en) * | 1970-11-12 | 1973-12-11 | Du Pont | Photosensitive bis-diazonium salt compositions and elements |
| US3847614A (en) * | 1971-09-13 | 1974-11-12 | Scott Paper Co | Diazo photopolymer composition and article comprising carboxylated resin |
| US3867154A (en) * | 1973-07-23 | 1975-02-18 | Keuffel & Esser Co | Desalination of silver halide photographic emulsions utilizing sulfated polyvinyl alcohol |
| US4433043A (en) * | 1980-11-18 | 1984-02-21 | Toppan Printing Co., Ltd. | Water based photosensitive composition with hydrolyzate of mammal collagen |
| US5432245A (en) * | 1990-04-02 | 1995-07-11 | Eastman Kodak Company | Method of coating thermoreversible heat-thickening polyacrylamides |
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