US2461474A - Gelatin subbing compositions having antistatic properties - Google Patents
Gelatin subbing compositions having antistatic properties Download PDFInfo
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- US2461474A US2461474A US716882A US71688246A US2461474A US 2461474 A US2461474 A US 2461474A US 716882 A US716882 A US 716882A US 71688246 A US71688246 A US 71688246A US 2461474 A US2461474 A US 2461474A
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- gelatin
- subbing
- solvent
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- water
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- 108010010803 Gelatin Proteins 0.000 title description 39
- 239000008273 gelatin Substances 0.000 title description 39
- 229920000159 gelatin Polymers 0.000 title description 39
- 235000019322 gelatine Nutrition 0.000 title description 39
- 235000011852 gelatine desserts Nutrition 0.000 title description 39
- 239000000203 mixture Substances 0.000 title description 38
- 229940014259 gelatin Drugs 0.000 description 38
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 27
- KZTYYGOKRVBIMI-UHFFFAOYSA-N diphenyl sulfone Chemical compound C=1C=CC=CC=1S(=O)(=O)C1=CC=CC=C1 KZTYYGOKRVBIMI-UHFFFAOYSA-N 0.000 description 19
- 239000002904 solvent Substances 0.000 description 19
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 239000000839 emulsion Substances 0.000 description 13
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 12
- 239000011248 coating agent Substances 0.000 description 7
- 238000000576 coating method Methods 0.000 description 7
- 230000003068 static effect Effects 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- 229920002301 cellulose acetate Polymers 0.000 description 6
- 239000011877 solvent mixture Substances 0.000 description 6
- 229920002678 cellulose Polymers 0.000 description 5
- 230000005611 electricity Effects 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 239000001913 cellulose Substances 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- -1 e. g. Chemical group 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 229920008347 Cellulose acetate propionate Polymers 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 3
- 238000009825 accumulation Methods 0.000 description 3
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 3
- HKQOBOMRSSHSTC-UHFFFAOYSA-N cellulose acetate Chemical compound OC1C(O)C(O)C(CO)OC1OC1C(CO)OC(O)C(O)C1O.CC(=O)OCC1OC(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C1OC1C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C(COC(C)=O)O1.CCC(=O)OCC1OC(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C1OC1C(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C(COC(=O)CC)O1 HKQOBOMRSSHSTC-UHFFFAOYSA-N 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- 239000002216 antistatic agent Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- PTMRDOLOEDPHLB-UHFFFAOYSA-N 2,3-dipentylphenol Chemical compound CCCCCC1=CC=CC(O)=C1CCCCC PTMRDOLOEDPHLB-UHFFFAOYSA-N 0.000 description 1
- 241000969130 Atthis Species 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- DQEFEBPAPFSJLV-UHFFFAOYSA-N Cellulose propionate Chemical compound CCC(=O)OCC1OC(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C1OC1C(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C(COC(=O)CC)O1 DQEFEBPAPFSJLV-UHFFFAOYSA-N 0.000 description 1
- 241000905957 Channa melasoma Species 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000000020 Nitrocellulose Substances 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
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 1
- 229920001727 cellulose butyrate Polymers 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 229920006218 cellulose propionate Polymers 0.000 description 1
- HGAZMNJKRQFZKS-UHFFFAOYSA-N chloroethene;ethenyl acetate Chemical compound ClC=C.CC(=O)OC=C HGAZMNJKRQFZKS-UHFFFAOYSA-N 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- MHDVGSVTJDSBDK-UHFFFAOYSA-N dibenzyl ether Chemical compound C=1C=CC=CC=1COCC1=CC=CC=C1 MHDVGSVTJDSBDK-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- KOWWOODYPWDWOJ-LVBPXUMQSA-N elatine Chemical compound C([C@]12CN(C3[C@@]45OCO[C@]44[C@H]6[C@@H](OC)[C@@H]([C@H](C4)OC)C[C@H]6[C@@]3([C@@H]1[C@@H]5OC)[C@@H](OC)CC2)CC)OC(=O)C1=CC=CC=C1N1C(=O)CC(C)C1=O KOWWOODYPWDWOJ-LVBPXUMQSA-N 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 231100000989 no adverse effect Toxicity 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 description 1
- 230000002522 swelling effect Effects 0.000 description 1
- 238000010792 warming 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
- G03C1/76—Photosensitive materials characterised by the base or auxiliary layers
- G03C1/85—Photosensitive materials characterised by the base or auxiliary layers characterised by antistatic additives or coatings
Definitions
- This invention relates to photographic film, and more particularly to gelatin subbing compositions ifav'ing antistatic properties.
- a film base is coated on one or both sides with a subbing composition which usually consists of a dispersion ofgelatin in a' suitable solvent or solvent mixture, so as to facilitate the adherence, or anchorage, of one or more of the photo-sensitive, non' curlin'g or anti-halation layers.
- a subbing composition which usually consists of a dispersion ofgelatin in a' suitable solvent or solvent mixture, so as to facilitate the adherence, or anchorage, of one or more of the photo-sensitive, non' curlin'g or anti-halation layers.
- An object of the present invention is to provide gelatin subbing compositions having anti-static properties.
- a further object is to providegelatin subbing compositions which reduce static charges on a photographic film baseduri'ng coating of the sen s'i'tive silver-halide emulsion, non-curl, or antihalation layers.
- R is veither hydrogen or an alkyl group of not more than 3 carbon atoms, e. g., methyl, ethyl, .propyl, amtisopropyl.
- the anti-static gelatin subbing compositions are prepared by adding the diphenylsulfone to a elatin dispersion containing gelatin, water, and a dispersing medium, and thereafter adding the dispersion to an organic solvent or mixture of such solvents, or by adding the diphenylsulfone to the finished gelatin subbing composition, 1. e., containing the organic solvent or mixtures thereof. Slight warming and agitation will facilitate the dissolution of the diphenylsulfone.
- the solution thus obtained is deposited on one or both sides of a film base in any convenient manner, the subbing operation preferably being carried out in connection with, or as apart of, the process of making the film support itself.
- the gelatin subbing solutions made up as above described are clear dispersions.
- the film bases used in accordance with this invention are the cellulose derivatives, e. g., cellulose nitrate, cellulose acetate, and other lower fatty acid esters of cellulose including simple and mixed esters, such as cellulose propionate, cellulose butyrate, cellulose acetate-propionate, cellulose acetate butyrate, and the like, ethers of cellulose, such as the ethyl ether, benzyl ether, and the like, and the fusible, water-insoluble, synthetic linear superpolymers used for film elements as described in United States Patents 2,071,250-2-3 and 2,130,948.
- cellulose derivatives e. g., cellulose nitrate, cellulose acetate, and other lower fatty acid esters of cellulose including simple and mixed esters, such as cellulose propionate, cellulose butyrate, cellulose acetate-propionate, cellulose acetate butyrate, and the like
- ethers of cellulose such as the
- each different type of cellulose ester, ether, and mixtures thereof, including the synthetic linear superpolymers requires a slightly different solvent or solvent combination.
- the solvent or solvent mixture employed must be such that it will have a solvent or at least a softening or swelling action on the film base so as to stick or anchor the gelatin upon the area of the support which has been softened or swollen.
- a cellulose acetate base a low molecular weight alcohol, e. g., methanol, ethanol, and the like, or a ketone, such as acetone or a mixture of 3 parts alcohol to one part of acetone may be employed.
- an alkyl ester such as, for example, methyl acetate, ethyl acetate, butyl acetate, and the like, either alone or with methanol or 1.4-dioxane may be effectively employed.
- the superpolymers there may be used mixtures of 'low molecular weight alcohols such as methanol, ethanol and the like, with phenols such as diamyl phenol and the like. It may be pointed out atthis point that the nature of the gelatin dispersing medium, solvent,
- r solvent mixture is immaterial so long as the dispersing medium, whether it be an organic acid, heterocyclic nitrogenous base, lactone, or the like, disperses the gelatin in water, and the solvent or solvent mixture wets or bites into the cellulose derivative or other materials employed as a film base.
- the term gelatin dispersed in a solvent for said support as used in the claims should be construed toembrace these dispersing mediums and solvent or solvent mixture. 'Since the-materials suitable for film base and their solvent properties are known, no difiicultyis pre sented in selecting a suitable solvent or solvent mixture for use in the subbing compositions.
- Example I A film base of cellulose acetate was coated with the following gelatinous substrating composition:
- the subbing layer had dried, the usual light-sensitive emulsion layer was coated directly thereon. During the coating of the light-sensitive emulsion upon the subbed base no static electricity was generated. After exposure and processing the emulsion adhered tenaciously to the cellulose acetate film support, and the developed film showed no black streaks or lines.
- Example II A film base of cellulose acetate-propionate having an acetyl content of 30% was coated with the following subbing composition:
- the subbing layer had dried, the usual light-sensitive emulsion layer was coated directly thereon. During the coating of the lightsensitive emulsion upon the subbed base no static electricity was generated. After exposure and processing the emulsion adhered tenaciously to the cellulose acetate film support, and the developed film showed no black streaks or lines.
- Example III A film base. prepared from poly (vinyl chloride-vinyl acetate) was coated with the following subbing composition:
- the subbing layer had dried, the usual light-sensitive emulsion layer was coated directly thereon. During the coating of the light-sensitive emulsion upon the subbed base no static electricity was generated. After exposure and processing the emulsion adhered tenaciously to the cellulose acetate film support, and the develexcellent as a sub for a synthetic linear polymer film base of the type described in United States Patents 2,071,250-2-3 and 2,130,948.
- the subbed photographic film bases produced according to the present invention in addition to preventing the accumulation of static electricity when unwound during a coating operation, were found to be very satisfactory from the standpoint of physical requirements, such as, high strength, flexibility, and good water-resistance.
- the small quantity of the diphenylsulfone which may remain with the gelatin after evaporation of the water and organic solvent from the subbing composition has no adverse effect upon the light-sensitive emulsion layer, nor has the subbing composition any adverse effect upon the containers in which it is stored, or upon the coating equipment employed.
- subbing is used, that such is intended to include the operation of applying a subbing layer from any one of the subbing compositions prepared in accordance with the present invention.
- An anti-static gelatin composition suitable for the subbing of a photographic film support which comprises a gelatin subbing composition containing from 0.5 to 1.5% of gelatin, from 1.33 to 15% of water, from 78 to 95.4% of a solvent for said support, and from 0.5 to of a diphenylsulfone of the following general formula:
- gelatin subbing composition containing from 0.5 to 1.5% of gelatin, from 1.33 to of water, from 78 to 95.4% of a solvent for said support, and from 0.5 to 10% of diphenylsulfone.
- An anti-static gelatin composition suitable for the subbing of a photographic film support which comprises a gelatin subbing composition containing from 0.5 to 1.5% of gelatin, from 1.3-3 to 15% of water, from '78 to 95.4% of a solvent for said support, and from 0.5 to 10% of 1,4-dimethyl-diphenylsulfone.
- An anti-static gelatin composition suitable for the subbing of a photographic film support which comprises a gelatin subbing composition containing from 0.5 to 1.5% of gelatin, from 1.33 to 15% of water, from '78 to 95.4% of a solvent for said support, and from 0.5 to 10% of 2,4,4-trimethyl-diphenylsulfone.
- a gelatin composition suitable for the subbing of a photographic film support which consists of the following constituents:
- a gelatin composition suitable for the subbing of a photographic film support which consists of the following constituents:
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
Patented Feb. 8, 1949 GELATIN SUBBIN G CQMPOSITI ONSHAZVING ANTESTATIC PROPERTIES Franl': J. K'aszuba, Binghaim'ton, N. Y1; design r to General Aniline & FilnijCorporation, New York, N. $1., a corporation of Delaware 2 No Drawing; Application ljecember 17,1946,-
Serial No. 716,882
7 Claims. (01. Ice-435') This invention relates to photographic film, and more particularly to gelatin subbing compositions ifav'ing antistatic properties.
- Considerable difliculty hasb'een encountered in the manufacture of photographic film due to the accumulation of electrical charges on the film. In one step of the manufacture of photographic film, a film base is coated on one or both sides with a subbing composition which usually consists of a dispersion ofgelatin in a' suitable solvent or solvent mixture, so as to facilitate the adherence, or anchorage, of one or more of the photo-sensitive, non' curlin'g or anti-halation layers. When such a laminate is wound into a tight roll and subsequently unwound, as during a coating oper-- ation, considerable static electricity is generated and spark discharges readily occur. Manifestations of these charges are glow discharges which after development of the 'coatedand exposed filni show up as black streaks or lines, or as irregular fogged patterns in the emulsion layer. Attempts have been made to overcome static in such laminates by the incorporation of substances into subbing compositions which are electrolytes or possess hygroscopic properties; The function of these substances is to impart conductivity to the film and thus dissipate the charges before their accumulation leads to local discharges. Many of these substances are incompatible with gelatin subbing compositions and introduce new manu: fac'turing difficulties.
An object of the present invention is to provide gelatin subbing compositions having anti-static properties.
A further object is to providegelatin subbing compositions which reduce static charges on a photographic film baseduri'ng coating of the sen s'i'tive silver-halide emulsion, non-curl, or antihalation layers. y
Further objects Will appear hereinafter.
These objects are accomplished by the present invention by ineorporating;'into any gelatin subbing composition, a diphenylsulfone of the followinggeneral formula:
wherein R is veither hydrogen or an alkyl group of not more than 3 carbon atoms, e. g., methyl, ethyl, .propyl, amtisopropyl.
As'suitable examples or 'dihenysuubnes, the following may be mentioned;
Y on;
2,4,4' Trinieth'yPdiphenylsul'fone 4nann-aip'iienyisunase" Th e;en ains" re nc r a e its any 'gela'tinsubbing composition containing gela tin; vvater, dispersing medium; such as as organic the balance being water, gelatin dispersing mediam,- and an organic solvent 01'. mixture of such solvents. A11 proportions are by weight;
The anti-static gelatin subbing compositions are prepared by adding the diphenylsulfone to a elatin dispersion containing gelatin, water, and a dispersing medium, and thereafter adding the dispersion to an organic solvent or mixture of such solvents, or by adding the diphenylsulfone to the finished gelatin subbing composition, 1. e., containing the organic solvent or mixtures thereof. Slight warming and agitation will facilitate the dissolution of the diphenylsulfone. The solution thus obtained is deposited on one or both sides of a film base in any convenient manner, the subbing operation preferably being carried out in connection with, or as apart of, the process of making the film support itself. The gelatin subbing solutions made up as above described are clear dispersions.
The film bases used in accordance with this invention are the cellulose derivatives, e. g., cellulose nitrate, cellulose acetate, and other lower fatty acid esters of cellulose including simple and mixed esters, such as cellulose propionate, cellulose butyrate, cellulose acetate-propionate, cellulose acetate butyrate, and the like, ethers of cellulose, such as the ethyl ether, benzyl ether, and the like, and the fusible, water-insoluble, synthetic linear superpolymers used for film elements as described in United States Patents 2,071,250-2-3 and 2,130,948.
It will be appreciated that each different type of cellulose ester, ether, and mixtures thereof, including the synthetic linear superpolymers, requires a slightly different solvent or solvent combination. The solvent or solvent mixture employed must be such that it will have a solvent or at least a softening or swelling action on the film base so as to stick or anchor the gelatin upon the area of the support which has been softened or swollen. For example, with a cellulose acetate base a low molecular weight alcohol, e. g., methanol, ethanol, and the like, or a ketone, such as acetone or a mixture of 3 parts alcohol to one part of acetone may be employed. With cellulose acetate-propionate film base, an alkyl ester, such as, for example, methyl acetate, ethyl acetate, butyl acetate, and the like, either alone or with methanol or 1.4-dioxane may be effectively employed. For the superpolymers there may be used mixtures of 'low molecular weight alcohols such as methanol, ethanol and the like, with phenols such as diamyl phenol and the like. It may be pointed out atthis point that the nature of the gelatin dispersing medium, solvent,
r solvent mixture is immaterial so long as the dispersing medium, whether it be an organic acid, heterocyclic nitrogenous base, lactone, or the like, disperses the gelatin in water, and the solvent or solvent mixture wets or bites into the cellulose derivative or other materials employed as a film base. The term gelatin dispersed in a solvent for said support as used in the claims should be construed toembrace these dispersing mediums and solvent or solvent mixture. 'Since the-materials suitable for film base and their solvent properties are known, no difiicultyis pre sented in selecting a suitable solvent or solvent mixture for use in the subbing compositions.
The following specific examples illustrate several of the various methods of applying these diphenylsulfones as antistatic agents in gelatin subbing compositions, and it will be understood that these examples merely represent the preferred embodiments and are not to he'considered as limitative.
Example I A film base of cellulose acetate was coated with the following gelatinous substrating composition:
Parts Gelatin 0.73 Water 1.33 Acetic acid 1.20 Diphenylsulfone 1.34 Methanol 75.53
Acetone 19.87
After the subbing layer had dried, the usual light-sensitive emulsion layer was coated directly thereon. During the coating of the light-sensitive emulsion upon the subbed base no static electricity was generated. After exposure and processing the emulsion adhered tenaciously to the cellulose acetate film support, and the developed film showed no black streaks or lines.
Example II A film base of cellulose acetate-propionate having an acetyl content of 30% was coated with the following subbing composition:
. Parts Gelatin s 1.0 Water 2.5 Acetic acid 1.5 4,4-Dimethy1-diphenylsulfone 1.0 Methanol 74.0 Methyl acetate 20.0
After the subbing layer had dried, the usual light-sensitive emulsion layer was coated directly thereon. During the coating of the lightsensitive emulsion upon the subbed base no static electricity was generated. After exposure and processing the emulsion adhered tenaciously to the cellulose acetate film support, and the developed film showed no black streaks or lines.
Example III A film base. prepared from poly (vinyl chloride-vinyl acetate) was coated with the following subbing composition:
Parts Gelatin 0.5
Water 2.5 Acetic acid 1.5 2,4,4-trimethyl-diphenylsulfone 1.5 Methanol 32.0 Acetone -1 62.0
After the subbing layer had dried, the usual light-sensitive emulsion layer was coated directly thereon. During the coating of the light-sensitive emulsion upon the subbed base no static electricity was generated. After exposure and processing the emulsion adhered tenaciously to the cellulose acetate film support, and the develexcellent as a sub for a synthetic linear polymer film base of the type described in United States Patents 2,071,250-2-3 and 2,130,948.
The subbed photographic film bases produced according to the present invention, in addition to preventing the accumulation of static electricity when unwound during a coating operation, were found to be very satisfactory from the standpoint of physical requirements, such as, high strength, flexibility, and good water-resistance.
The small quantity of the diphenylsulfone which may remain with the gelatin after evaporation of the water and organic solvent from the subbing composition, has no adverse effect upon the light-sensitive emulsion layer, nor has the subbing composition any adverse effect upon the containers in which it is stored, or upon the coating equipment employed.
It will be understood that wherein the claims appended hereto the term subbing is used, that such is intended to include the operation of applying a subbing layer from any one of the subbing compositions prepared in accordance with the present invention.
While the present invention has been described in considerable detail with respect to certain preferred materials, it is understood that the class of gelatin dispersing agents, solvents, or mixture of such solvents is not limited thereto and that numerous variations and modifications described in the foregoing specification may be made. As for example, a mixture of two or more of the diphenylsulfones may be employed as anti-static agents. Similarly, a film support may be coated on both sides with the subbing compositions prepared in accordance with the present invention for the preparation of X-ray film, wherein both subbed sides are coated with a suitable gelatino silver-halide emulsion.
I claim:
1. An anti-static gelatin composition suitable for the subbing of a photographic film support, which comprises a gelatin subbing composition containing from 0.5 to 1.5% of gelatin, from 1.33 to 15% of water, from 78 to 95.4% of a solvent for said support, and from 0.5 to of a diphenylsulfone of the following general formula:
which comprises a gelatin subbing composition containing from 0.5 to 1.5% of gelatin, from 1.33 to of water, from 78 to 95.4% of a solvent for said support, and from 0.5 to 10% of diphenylsulfone.
3. An anti-static gelatin composition suitable for the subbing of a photographic film support, which comprises a gelatin subbing composition containing from 0.5 to 1.5% of gelatin, from 1.3-3 to 15% of water, from '78 to 95.4% of a solvent for said support, and from 0.5 to 10% of 1,4-dimethyl-diphenylsulfone.
4. An anti-static gelatin composition suitable for the subbing of a photographic film support, which comprises a gelatin subbing composition containing from 0.5 to 1.5% of gelatin, from 1.33 to 15% of water, from '78 to 95.4% of a solvent for said support, and from 0.5 to 10% of 2,4,4-trimethyl-diphenylsulfone.
5. A gelatin composition suitable for the subbing of a photographic film support which consists of the following constituents:
Parts by weight Gelatin 0.73 Water 1.33 Acetic acid 1.20 Diphenyls'ulfone 1.34 Methanol 75.53 Acetone 19.87
6. A gelatin composition suitable for the subbing of a photographic film support which consists of the following constituents:
Parts by weight Gelatin 1.0 Water 2.5 Acetic acid 1.5 4,4-dimethyl-diphenylsulfone 1.0 Methanol 74.0 Methyl acetate 20.0
7. A gelatin composition suitable for the sub- 1,; bing of a photographic film support which consists of the following constituents:
Parts by weight Gelatin 0.5 Water 2.5 Acetic acid 1.5- 2,4,4'-trimethy1- diphenylsulf one 1.5 Methanol 32.0 Acetone 62.0
FRANK J. KASZUBA.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 2,341,887 Middleton et al. Feb. 15, 1944 2,313,570 Nadeau et al. Mar. 9, 1943-
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US716882A US2461474A (en) | 1946-12-17 | 1946-12-17 | Gelatin subbing compositions having antistatic properties |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US716882A US2461474A (en) | 1946-12-17 | 1946-12-17 | Gelatin subbing compositions having antistatic properties |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2461474A true US2461474A (en) | 1949-02-08 |
Family
ID=24879840
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US716882A Expired - Lifetime US2461474A (en) | 1946-12-17 | 1946-12-17 | Gelatin subbing compositions having antistatic properties |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2461474A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2805964A (en) * | 1956-04-04 | 1957-09-10 | Pennsalt Chemical Corp | Treatment of plastics |
| US3475203A (en) * | 1964-10-21 | 1969-10-28 | Bexford Ltd | Hydrophobic film rendered antistatic by phenol-formaldehyde resin derivatives |
| US3779773A (en) * | 1971-02-08 | 1973-12-18 | T Inayama | Static charge-prevented photographic light sensitive element |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2313570A (en) * | 1940-09-25 | 1943-03-09 | Eastman Kodak Co | Photographic layer capable of receiving writing |
| US2341887A (en) * | 1941-06-26 | 1944-02-15 | Chemical Construction Corp | Cooling of sulphur dioxide gases |
-
1946
- 1946-12-17 US US716882A patent/US2461474A/en not_active Expired - Lifetime
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2313570A (en) * | 1940-09-25 | 1943-03-09 | Eastman Kodak Co | Photographic layer capable of receiving writing |
| US2341887A (en) * | 1941-06-26 | 1944-02-15 | Chemical Construction Corp | Cooling of sulphur dioxide gases |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2805964A (en) * | 1956-04-04 | 1957-09-10 | Pennsalt Chemical Corp | Treatment of plastics |
| US3475203A (en) * | 1964-10-21 | 1969-10-28 | Bexford Ltd | Hydrophobic film rendered antistatic by phenol-formaldehyde resin derivatives |
| US3779773A (en) * | 1971-02-08 | 1973-12-18 | T Inayama | Static charge-prevented photographic light sensitive element |
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