US2370321A - Soluble photographic layers of colloidal gums and process for conditioning such gumsfor such use - Google Patents
Soluble photographic layers of colloidal gums and process for conditioning such gumsfor such use Download PDFInfo
- Publication number
- US2370321A US2370321A US440430A US44043042A US2370321A US 2370321 A US2370321 A US 2370321A US 440430 A US440430 A US 440430A US 44043042 A US44043042 A US 44043042A US 2370321 A US2370321 A US 2370321A
- Authority
- US
- United States
- Prior art keywords
- agar
- soluble
- conditioning
- gumsfor
- layers
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 230000003750 conditioning effect Effects 0.000 title description 3
- 238000000034 method Methods 0.000 title description 3
- 102000004190 Enzymes Human genes 0.000 description 15
- 108090000790 Enzymes Proteins 0.000 description 15
- 239000000084 colloidal system Substances 0.000 description 15
- 229940088598 enzyme Drugs 0.000 description 15
- 239000010410 layer Substances 0.000 description 13
- 229920001817 Agar Polymers 0.000 description 11
- 241000206672 Gelidium Species 0.000 description 11
- 235000010419 agar Nutrition 0.000 description 11
- 235000014633 carbohydrates Nutrition 0.000 description 11
- 150000001720 carbohydrates Chemical class 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- 239000012790 adhesive layer Substances 0.000 description 7
- 230000007062 hydrolysis Effects 0.000 description 6
- 238000006460 hydrolysis reaction Methods 0.000 description 6
- 235000018102 proteins Nutrition 0.000 description 6
- 102000004169 proteins and genes Human genes 0.000 description 6
- 108090000623 proteins and genes Proteins 0.000 description 6
- -1 VIP carbohydrate Chemical class 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 102000035195 Peptidases Human genes 0.000 description 3
- 108091005804 Peptidases Proteins 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 229910052709 silver Inorganic materials 0.000 description 3
- 239000004332 silver Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 230000003301 hydrolyzing effect Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 239000001828 Gelatine Substances 0.000 description 1
- 229920000715 Mucilage Polymers 0.000 description 1
- 102000057297 Pepsin A Human genes 0.000 description 1
- 108090000284 Pepsin A Proteins 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004133 Sodium thiosulphate Substances 0.000 description 1
- 102000004142 Trypsin Human genes 0.000 description 1
- 108090000631 Trypsin Proteins 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 239000002313 adhesive film Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 235000010980 cellulose Nutrition 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229940111202 pepsin Drugs 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 235000004252 protein component Nutrition 0.000 description 1
- 230000002797 proteolythic effect Effects 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- 239000012588 trypsin Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
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
- G03C1/76—Photosensitive materials characterised by the base or auxiliary layers
- G03C1/805—Photosensitive materials characterised by the base or auxiliary layers characterised by stripping layers or stripping means
Definitions
- the present invention relates to soluble photographic layers prepared from agar-agarand to the use of such layers as an adhesive in stripfilm.
- colloids are extensively used in photography in the manufacture of layers such as surface-, back-, and anti-halation layers and adhesive layers. In the latter case they are extensively employed in the formation of the so-called photographicstrip film.
- Such film essentially comprises, in'the order of their arrangement, a temporary support, a strip or adhesive layer, a permanent support and a photographic emulsion.
- the prior art has proposed to utilize for this purpose such colloids as soluble gelatine, glues, dextrines' and the like.
- colloids may also be employed for the formation of the other layers previously mentioned, the character or property in question permitting them when cast into layers to be united directly to the film base or other layers thereon.
- the acids serve to catalyse hydrolytic reactions independently of the nature of the colloid hydrolysed or ofthe'bonds to be hydrolysed. Thus, they operate equally on carbohydrates, proteins or fats, the degree of hydrolysis being dependent to a certain extent at least upon the duration of their action.
- agar-agar-differs from most colloids such as carsgeen, extract of lichen and the like, which are capable of beingsolubilizedto the desired de ree by the utilization of a single type of enzyme.
- Suitable enzymes of the proteolytic type is the product sold by Roehm 8: Haas Co.,
- the degree-of solubility of the degraded agaragar will depend to some extent on the agent employed but it is .to be emphasized again that the hydrolysis must be carried to such an extent that a product readily soluble in the usual aqueous fixing, baths will ensue. However, the, time of treatment must not be extended so far as to result in products sticky in character. Because the extent of treatment will vary, a specific statement of time cannot be given. This, however, is immaterial since a simple test will enable the operator to determine when he is within the limits just given.
- the invention is further exemplified by the accompanying self-explanatory drawing and the following examples, but it is to be understood that the examples are merely illustrative of the invention.
- the drawing illustrates in section in Fig. I strip film containing a colloid treated according to the invention, as the adhesive layer and in Fig. H film carrying a layer of a colloid treated according to the invention as an antihalation backing.
- Example 1 A solution of 2.5% of agar-agar in 2% acetic acid is heated to boiling for 15 to minutes, and thereafter quickly cooled. The filtered solution is cast to form the adhesive layer B in the film of Fig. I. The adhesive film dries with a smooth and even surface without showing any signs of stickiness.
- Example 2 I A solution of agar-agar treated as in Example 1 is cast to provide the anti-halation backing R of-Fig. II.
- This film, as well as that of Fig. I, is soluble in water and mixes readily with antihalation dyes.
- To facilitate coating there may be incorporated in the solution a suli'onated carboxylic acid amide of the type disclosed in U. 8. Patent 1,932,179.
- Example 3 A 5% solution of agar-agar, disinfected with phenol, is buffered to pH 4.5 with Mcllvaine buffer (Handbook of Chemistry and Physics, 16th edition, page 577). 250 mg. per liter of the product sold by the Roehm 8r Haas Co. of Philadelphia, Pa., under the trade-mark Pectincl 100" are added and the solution kept in an incubator for 48 hours at 45 C. The pH is then increased to 7.5 whereupon 250 mg. per liter oi the product sold by Roehm 8r Haas under the trade-mark Qrthozyme X are added and again the solution held in the incubator for 72 hours. After removal from the incubator, the solution is heated to to C. to stop the action of the enzymes. The solution is filtered while hot from undissolved particles and may then be used in strip film, surfaceand anti-halation coatings and the like.
- a photographic strip film comprising a permanent support having a silver halide emulsion thereon and a temporary support and containing as the adhesive layer between the temporary and permanent supports the hydrolyzed colloid prepared by subjecting an agar-agar high in nitrogen to hydrolysis by means of a hydrolyzing agent selected from the class consisting of free acids and a combination of enzymes employed in sequence, while heating until the colloid becomes readily soluble in the usual aqueous fixing baths and when cast forms a transparent non-sticky layer.
- a hydrolyzing agent selected from the class consisting of free acids and a combination of enzymes employed in sequence
- a photographic strip film comprising a permanent support having a silver halide emulsion thereon and a temporary support and containing as the adhesive layer between the temporary and permanent supports the hydrolysed colloid prepared by subjecting agar-agar to hydrolysis by means of a free acid while heating until the colloid becomes readily soluble in the usual aqueous fixing baths and when cast forms a transparent, non-sticky layer.
- a photographic strip film comprising a permanent support having a silver halide emulslon thereon and a temporary support and containing as the adhesive layer between the temporary and permanent supports the hydrolyzed colloid prepared by heating agar-agar with acetic acid until the agar-agar becomes readily soluble in the usual aqueous fixing baths and when cast forms a transparent, non-sticky layer.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Laminated Bodies (AREA)
Description
Feb. 27, 1945. I F. w. H. MUELLER 2,370,321
SOLUBLE PHOTOGRAPHIC LAYERS OF COLLOIDAL GUMS AND PROCESS FOR CONDITIONING SUCH GUMS FOR SUCH USE Filed April 25, 1942 g sure-e H44 ms 9' Z Era/4am LAYEE A pseflan/swrsuppaer 6/41/52 HAL/0E EMULSION ans-2 INVENTOR fik/rz G1 64 Mar-245E TTO NEYS Patented Feb. 27, 1945 UNITED STATES PATENT OFFICE SOLUBLE PHOTOGBAPHIC LAYERS OF COLLOIDAL GUMS AND PROCESS FOR CONDITIONING SUCH GUMS FOR SUCH- Fritz w. n. Mueller, Binghamton, N. Y. Application April 25, 1942, Serial No. 440,430
Claims.
The present invention relates to soluble photographic layers prepared from agar-agarand to the use of such layers as an adhesive in stripfilm. This application constitutes a continuationin-part of my prior application Serial No. 357,609, filed September 20, 1940, now U. S. P. 2,330,905.
Colloids are extensively used in photography in the manufacture of layers such as surface-, back-, and anti-halation layers and adhesive layers. In the latter case they are extensively employed in the formation of the so-called photographicstrip film. Such film, as known, essentially comprises, in'the order of their arrangement, a temporary support, a strip or adhesive layer, a permanent support and a photographic emulsion. The prior art has proposed to utilize for this purpose such colloids as soluble gelatine, glues, dextrines' and the like. Inasmuch as such colloids are naturally of an adheslve character, they may also be employed for the formation of the other layers previously mentioned, the character or property in question permitting them when cast into layers to be united directly to the film base or other layers thereon.
Such substances have certain disadvantages when used in these relationships. In U. 8. P. 2,275,617 it was proposed to overcome these disadvantages, particularly in the manufacture of adhesives for strip film, by employing in lieu of said colloids certain vegetable mucilages and pecto celluloses. It was round that these substances exhibited the peculiar property of having the viscosity thereof greatly diminished by photographic fixing baths, particularly those containing sodium thiosulphate, so that when strip film containing the same was immersed in such baths, the bond between the temporary support and the pent support was destroyed. It was further noted in said patent that this property is not common to all colloids, and in this connection reference was made inter alia to agaragsr. This substance, though good dition it for use as a strip film adhesive by increasing its solubility without impairing its VIP carbohydrate component intact.
acid, acetic acid, formic acid, propionic acid and the like. The acids serve to catalyse hydrolytic reactions independently of the nature of the colloid hydrolysed or ofthe'bonds to be hydrolysed. Thus, they operate equally on carbohydrates, proteins or fats, the degree of hydrolysis being dependent to a certain extent at least upon the duration of their action.
The same; however, does not apply to the action of enzymes. the material treated, different enzymes being required for carbohydrates, proteins and the like. Thus, for instance, the application of a carbohydrate splitting enzyme will leave the protein component entirely intact, whereas the application of a protein splitting enzyme will leave the Agar-agar as is known from the literature contains about 17% of proteins and about 40% of water-soluble carbohydrates, known as gelose (GRAFE, Hdb. org. Wk (1931), vol. 112,
page 730) Due to the high protein content and carbohydrate content of agar-agar, it is not possible to hydrolyse or degrade the same to the extent that the resulting product will be soluble in the usual aqueous fixing baths by utilizing a carbohydrate splitting enzyme alone or a protein splitting enzyme (proteolytic enzyme) alone. On the contrary, in order to obtain the desired degree of hydrolysis, it is necessary to use both a proteolytic enzyme and a carbohydrate splitting enzyme in sequence, it being immaterial, however, which of the two enzymes is first employed. In this respect, agar-agar-differs from most colloids, such as carsgeen, extract of lichen and the like, which are capable of beingsolubilizedto the desired de ree by the utilization of a single type of enzyme. Suitable enzymes of the proteolytic type is the product sold by Roehm 8: Haas Co.,
' so Philadelphia, Pa., under the trade mark Orthozyme X (activated trypsin), pepsin and the like. Suitable enzymes of the carbohydrate splitting type are the products sold by Roehm it Haas 00., Philadelphil. Pm. under the trade mark "Pectinol 100," and containing pectinssc as the Their action is specific as regards bohydrate splitting enzymes, the application being in sequence, as previously stated.
The degree-of solubility of the degraded agaragar will depend to some extent on the agent employed but it is .to be emphasized again that the hydrolysis must be carried to such an extent that a product readily soluble in the usual aqueous fixing, baths will ensue. However, the, time of treatment must not be extended so far as to result in products sticky in character. Because the extent of treatment will vary, a specific statement of time cannot be given. This, however, is immaterial since a simple test will enable the operator to determine when he is within the limits just given.
The invention is further exemplified by the accompanying self-explanatory drawing and the following examples, but it is to be understood that the examples are merely illustrative of the invention. The drawing illustrates in section in Fig. I strip film containing a colloid treated according to the invention, as the adhesive layer and in Fig. H film carrying a layer of a colloid treated according to the invention as an antihalation backing.
Example 1 A solution of 2.5% of agar-agar in 2% acetic acid is heated to boiling for 15 to minutes, and thereafter quickly cooled. The filtered solution is cast to form the adhesive layer B in the film of Fig. I. The adhesive film dries with a smooth and even surface without showing any signs of stickiness.
Example 2 I A solution of agar-agar treated as in Example 1 is cast to provide the anti-halation backing R of-Fig. II. This film, as well as that of Fig. I, is soluble in water and mixes readily with antihalation dyes. To facilitate coating there may be incorporated in the solution a suli'onated carboxylic acid amide of the type disclosed in U. 8. Patent 1,932,179.
Example 3 A 5% solution of agar-agar, disinfected with phenol, is buffered to pH 4.5 with Mcllvaine buffer (Handbook of Chemistry and Physics, 16th edition, page 577). 250 mg. per liter of the product sold by the Roehm 8r Haas Co. of Philadelphia, Pa., under the trade-mark Pectincl 100" are added and the solution kept in an incubator for 48 hours at 45 C. The pH is then increased to 7.5 whereupon 250 mg. per liter oi the product sold by Roehm 8r Haas under the trade-mark Qrthozyme X are added and again the solution held in the incubator for 72 hours. After removal from the incubator, the solution is heated to to C. to stop the action of the enzymes. The solution is filtered while hot from undissolved particles and may then be used in strip film, surfaceand anti-halation coatings and the like.
I claim:
1. A photographic strip film comprising a permanent support having a silver halide emulsion thereon and a temporary support and containing as the adhesive layer between the temporary and permanent supports the hydrolyzed colloid prepared by subjecting an agar-agar high in nitrogen to hydrolysis by means of a hydrolyzing agent selected from the class consisting of free acids and a combination of enzymes employed in sequence, while heating until the colloid becomes readily soluble in the usual aqueous fixing baths and when cast forms a transparent non-sticky layer.
2. The photographic strip film of claim 1, wherein the hydrolyzed colloid is prepared by the action in sequence of a carbohydrate splitting enzyme and a proteolytic enzyme. v
3. The article defined in claim 1 wherein the agar-agar subjected to hydrolysis contains on the order of 17 per cent of proteins and about 40 per cent of water-soluble carbohydrates.
. 4. A photographic strip film comprising a permanent support having a silver halide emulsion thereon and a temporary support and containing as the adhesive layer between the temporary and permanent supports the hydrolysed colloid prepared by subjecting agar-agar to hydrolysis by means of a free acid while heating until the colloid becomes readily soluble in the usual aqueous fixing baths and when cast forms a transparent, non-sticky layer.
5. A photographic strip film comprising a permanent support having a silver halide emulslon thereon and a temporary support and containing as the adhesive layer between the temporary and permanent supports the hydrolyzed colloid prepared by heating agar-agar with acetic acid until the agar-agar becomes readily soluble in the usual aqueous fixing baths and when cast forms a transparent, non-sticky layer.
FRITZ W. H. MUELLER.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US440430A US2370321A (en) | 1942-04-25 | 1942-04-25 | Soluble photographic layers of colloidal gums and process for conditioning such gumsfor such use |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US440430A US2370321A (en) | 1942-04-25 | 1942-04-25 | Soluble photographic layers of colloidal gums and process for conditioning such gumsfor such use |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2370321A true US2370321A (en) | 1945-02-27 |
Family
ID=23748729
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US440430A Expired - Lifetime US2370321A (en) | 1942-04-25 | 1942-04-25 | Soluble photographic layers of colloidal gums and process for conditioning such gumsfor such use |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2370321A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2602741A (en) * | 1945-11-01 | 1952-07-08 | Grinten Chem L V D | Sensitized sheets for screen reflectography |
| US2805948A (en) * | 1955-06-27 | 1957-09-10 | Gen Aniline & Film Corp | Photographic stripping film |
| WO1980002879A1 (en) * | 1979-06-21 | 1980-12-24 | Minnesota Mining & Mfg | Composite photographic structure |
| US4407932A (en) * | 1981-03-12 | 1983-10-04 | Minnesota Mining & Manufacturing Co. | Fade-resistant and abrasion resistant photographic reproduction, method of preparing, and photographic product therefor |
-
1942
- 1942-04-25 US US440430A patent/US2370321A/en not_active Expired - Lifetime
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2602741A (en) * | 1945-11-01 | 1952-07-08 | Grinten Chem L V D | Sensitized sheets for screen reflectography |
| US2805948A (en) * | 1955-06-27 | 1957-09-10 | Gen Aniline & Film Corp | Photographic stripping film |
| WO1980002879A1 (en) * | 1979-06-21 | 1980-12-24 | Minnesota Mining & Mfg | Composite photographic structure |
| US4407932A (en) * | 1981-03-12 | 1983-10-04 | Minnesota Mining & Manufacturing Co. | Fade-resistant and abrasion resistant photographic reproduction, method of preparing, and photographic product therefor |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US2596756A (en) | Photomechanical copy method | |
| US4092168A (en) | Light-absorbing dyes for silver halide material | |
| GB632402A (en) | Photographic stripping film and paper | |
| US2370321A (en) | Soluble photographic layers of colloidal gums and process for conditioning such gumsfor such use | |
| GB454499A (en) | Improvements in colour photography | |
| US2330905A (en) | Soluble photographic layer of colloidal gums and process of conditioning such gums for such use | |
| US3565618A (en) | Photographic colloid transfer facilitated by enzyme treatment | |
| US2089460A (en) | Process for fastening a photographic material on a support and the resulting product | |
| US3511657A (en) | Method of stripping gelatin emulsions from polyester supports | |
| US2319102A (en) | Adhesive | |
| US2725293A (en) | Photographic emulsion compositions and their preparation | |
| US2725305A (en) | Hardening gelatin emulsions and gelatin solutions | |
| US3749573A (en) | Silver halide photosensitive element containing hydrophilic colloid layers hardened with alpha,beta-bis-acryloylamido-ethyleneglycol | |
| US3157506A (en) | Photographic film base subbed with acid-cooked pigskin gelatin | |
| GB489299A (en) | Improvements in or relating to the chemical treatment of photographic images | |
| US3441412A (en) | Photographic silver halide material containing carboxyalkylated dextrin | |
| GB499648A (en) | Improved process of hardening photographic silver halide emulsion layers and other layers containing protein | |
| GB820322A (en) | Improved methods of preparing silver halide dispersions and photographic emulsions | |
| GB547740A (en) | Improvements relating to photographic materials | |
| US2317750A (en) | System of improving photographic layers | |
| US2481676A (en) | Hardened polyvinyl alcohol silver halide photographic coatings | |
| US2338672A (en) | Method of recovering film scrap | |
| US3250620A (en) | Silver halide emulsions having chill-setting properties | |
| US5604083A (en) | Antistatic film bases and photographic elements comprising said antistatic film bases | |
| US3382077A (en) | Binding agents for photographic hydrophilic colloid layers which are crosslinked by treatment with alkalis |