GB544006A - Improvements in sensitive photographic elements - Google Patents
Improvements in sensitive photographic elementsInfo
- Publication number
- GB544006A GB544006A GB14235/40A GB1423540A GB544006A GB 544006 A GB544006 A GB 544006A GB 14235/40 A GB14235/40 A GB 14235/40A GB 1423540 A GB1423540 A GB 1423540A GB 544006 A GB544006 A GB 544006A
- Authority
- GB
- United Kingdom
- Prior art keywords
- grams
- phthalate
- carbon
- mixed
- colloid
- 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
Links
- 239000000084 colloidal system Substances 0.000 abstract 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 6
- 229910052799 carbon Inorganic materials 0.000 abstract 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 4
- 239000006229 carbon black Substances 0.000 abstract 4
- 239000000463 material Substances 0.000 abstract 4
- 239000000203 mixture Substances 0.000 abstract 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 4
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 abstract 3
- 239000011230 binding agent Substances 0.000 abstract 3
- 229920002678 cellulose Polymers 0.000 abstract 3
- 239000002270 dispersing agent Substances 0.000 abstract 3
- 235000019441 ethanol Nutrition 0.000 abstract 3
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 abstract 2
- 229920000623 Cellulose acetate phthalate Polymers 0.000 abstract 2
- 229940081734 cellulose acetate phthalate Drugs 0.000 abstract 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 abstract 2
- 150000001991 dicarboxylic acids Chemical class 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- 239000003960 organic solvent Substances 0.000 abstract 2
- 239000002245 particle Substances 0.000 abstract 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 abstract 2
- 229940100467 polyvinyl acetate phthalate Drugs 0.000 abstract 2
- URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 abstract 2
- 229920002554 vinyl polymer Polymers 0.000 abstract 2
- KWVPFECTOKLOBL-KTKRTIGZSA-N 2-[(z)-octadec-9-enoxy]ethanol Chemical compound CCCCCCCC\C=C/CCCCCCCCOCCO KWVPFECTOKLOBL-KTKRTIGZSA-N 0.000 abstract 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 abstract 1
- 239000002202 Polyethylene glycol Substances 0.000 abstract 1
- UTKBLLDLHPDWDU-ODZAUARKSA-N acetic acid;(z)-but-2-enedioic acid Chemical compound CC(O)=O.OC(=O)\C=C/C(O)=O UTKBLLDLHPDWDU-ODZAUARKSA-N 0.000 abstract 1
- QDAFGQZLEVTNMR-UAIGNFCESA-N acetic acid;(z)-but-2-enedioic acid;propanoic acid Chemical compound CC(O)=O.CCC(O)=O.OC(=O)\C=C/C(O)=O QDAFGQZLEVTNMR-UAIGNFCESA-N 0.000 abstract 1
- IYKJEILNJZQJPU-UHFFFAOYSA-N acetic acid;butanedioic acid Chemical compound CC(O)=O.OC(=O)CCC(O)=O IYKJEILNJZQJPU-UHFFFAOYSA-N 0.000 abstract 1
- PXZFYPYSGHNODK-UHFFFAOYSA-N acetic acid;butanedioic acid;propanoic acid Chemical compound CC(O)=O.CCC(O)=O.OC(=O)CCC(O)=O PXZFYPYSGHNODK-UHFFFAOYSA-N 0.000 abstract 1
- 239000000443 aerosol Substances 0.000 abstract 1
- 239000003513 alkali Substances 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 238000000576 coating method Methods 0.000 abstract 1
- 239000007859 condensation product Substances 0.000 abstract 1
- SVOAENZIOKPANY-CVBJKYQLSA-L copper;(z)-octadec-9-enoate Chemical compound [Cu+2].CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O SVOAENZIOKPANY-CVBJKYQLSA-L 0.000 abstract 1
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Natural products CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 abstract 1
- 238000007865 diluting Methods 0.000 abstract 1
- 239000006185 dispersion Substances 0.000 abstract 1
- 239000000839 emulsion Substances 0.000 abstract 1
- DQYBDCGIPTYXML-UHFFFAOYSA-N ethoxyethane;hydrate Chemical compound O.CCOCC DQYBDCGIPTYXML-UHFFFAOYSA-N 0.000 abstract 1
- 239000001087 glyceryl triacetate Substances 0.000 abstract 1
- 235000013773 glyceryl triacetate Nutrition 0.000 abstract 1
- 238000003801 milling Methods 0.000 abstract 1
- 238000002156 mixing Methods 0.000 abstract 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 abstract 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 abstract 1
- 239000003973 paint Substances 0.000 abstract 1
- KQOCPYKMLMTOOP-UHFFFAOYSA-N phthalic acid;propanoic acid Chemical compound CCC(O)=O.OC(=O)C1=CC=CC=C1C(O)=O KQOCPYKMLMTOOP-UHFFFAOYSA-N 0.000 abstract 1
- 239000004014 plasticizer Substances 0.000 abstract 1
- 229920001223 polyethylene glycol Polymers 0.000 abstract 1
- 229920001290 polyvinyl ester Polymers 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 229920005989 resin Polymers 0.000 abstract 1
- 239000011347 resin Substances 0.000 abstract 1
- 239000000344 soap Substances 0.000 abstract 1
- 150000003385 sodium Chemical class 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 229920003002 synthetic resin Polymers 0.000 abstract 1
- 239000000057 synthetic resin Substances 0.000 abstract 1
- 229960002622 triacetin Drugs 0.000 abstract 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
- G03C1/825—Photosensitive materials characterised by the base or auxiliary layers characterised by antireflection means or visible-light filtering means, e.g. antihalation
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
544,006. Photographic light-sensitive material. KODAK, Ltd. (Eastman Kodak Co., and Simmons, N. L.). Sept. 16, 1940, Nos. 14235/40 and 10700/41. [Class 98 (ii)] Photographic material has on a support at least one light-sensitive emulsion layer and a layer, especially an anti-halation layer, consisting of carbon particles dispersed in a water-insoluble alkali- or acid-soluble binder. The carbon particles may be below 60 mÁ, preferably 30 mÁ in average diameter. The alkali-soluble binders may be synthetic resins, e.g. polyvinyl esters of dicarboxylic acids, or cellulose esters, e.g. cellulose esters of dicarboxylic acids, or mixed esters of mono- and di-carboxylic acids. Suitable resins are polyvinyl phthalate and polyvinyl acetate phthalate, and suitable cellulose esters are cellulose acetate phthalate, acetate maleate, acetate succinate, propionate phthalate, acetate propionate maleate, and acetate propionate succinate. The carbon may be dispersed in the colloid by using a mechanical disintegrator or colloid mill, or may be dispersed in a solution of the colloid using a dispersing agent such as water-insoluble metallic soap, an Aerosol (a sulphonated ester of a dicarboxylic acid), or Novonacco (a modified sodium alkyl naphthalene sulphonate). The carbon should preferably be mixed with the colloid itself, little or no solvent being present during disintegration. The carbon may be mixed with the colloid in the dry state and a small quantity of plasticizer added and after further mixing the mixture is fed between the rolls of a mill of the type used in the rubber industry. The rolls may be heated or cooled in order that the mass shall exhibit an unusually high consistency. In example (1), 500 grams of cellulose acetate phthalate, 200 grams of carbon black, and 200 grams of methyl carbitol are mixed with a paddle and fed into the rolls of a rubber mill, the rolls being water cooled to maintain a maximum temperature of 180F. After 15 minutes' milling, the sheet of material wrapped completely about the faster roll is stripped off and allowed to cool. 75 grams of the material are dissolved in 270 grams of ethylene glycol methyl ether, 160 grams of water, 10 grams of acetone, and 380 grams of ethyl alcohol, and coated on a support to form an anti-halation layer. The coatings may also be used in the preparation of leaders and anti-static layers. The methyl carbitol may be replaced by ethylene glycol methyl ether, triacetin, or dibutyl phthalate. Carbon black in the form of a paste containing as dispersing agent copper oleate, stearate, or resinate, or dry carbon black may be formed into a paste with water containing a dispersing agent and a small amount of alkali. The paste may be mixed with an organic solvent and added to the binder dissolved in organic solvents and coated. In example (2), colloidal carbon paste is dispersed in a mixture of water and ethylene glycol monomethyl ether and a solution of polyvinyl phthalate in acetone and methyl alcohol is added. The mixture is run through a colloid mill, diluted with methyl alcohol, and coated. In example (3), carbon black is mixed with " Emulphor 0" (Registered Trade Mark), which is a polyethylene glycol condensation product, in ethyl alcohol to form a paste, a solution of polyvinyl acetate phthalate in ethyl alcohol added, the mixture passed several times through a paint or colloid mill, and, after diluting, the dispersion is coated. Specification 537,081 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US385277A US2327828A (en) | 1941-03-26 | 1941-03-26 | Colloidal carbon antihalation layer |
Publications (1)
Publication Number | Publication Date |
---|---|
GB544006A true GB544006A (en) | 1942-03-24 |
Family
ID=23520746
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB14235/40A Expired GB544006A (en) | 1941-03-26 | 1940-09-16 | Improvements in sensitive photographic elements |
Country Status (4)
Country | Link |
---|---|
US (1) | US2327828A (en) |
DE (1) | DE893009C (en) |
FR (3) | FR937743A (en) |
GB (1) | GB544006A (en) |
Families Citing this family (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR960188A (en) * | 1947-01-28 | 1950-04-14 | ||
US2694662A (en) * | 1950-06-10 | 1954-11-16 | Eastman Kodak Co | Opaque sheeting and method of making same |
US2716060A (en) * | 1950-07-07 | 1955-08-23 | Direct Reproduction Corp | Contact printing emulsion and method of making |
US2968582A (en) * | 1958-09-22 | 1961-01-17 | Eastman Kodak Co | Film products having pectin layers |
DE1422890A1 (en) * | 1961-05-08 | 1969-10-23 | Gevaert Photo Prod Nv | Antistatic photographic material and method for making the same |
US3222178A (en) * | 1961-10-09 | 1965-12-07 | Eastman Kodak Co | Composite film element |
BE669912A (en) * | 1964-09-29 | 1966-01-17 | ||
US3516832A (en) * | 1966-11-25 | 1970-06-23 | Eastman Kodak Co | Photographic articles and materials useful in their manufacture |
US3849191A (en) * | 1966-11-25 | 1974-11-19 | Eastman Kodak Co | Photographic articles and materials useful in their manufacture |
US4301239A (en) * | 1979-12-05 | 1981-11-17 | E. I. Du Pont De Nemours And Company | Antistatic backing layer for unsubbed polyester film |
JPS5952647A (en) * | 1982-06-30 | 1984-03-27 | 富士写真フイルム株式会社 | Mat film which can be corrected |
US5679505A (en) | 1995-11-02 | 1997-10-21 | Eastman Kodak Company | Photographic element useful as a motion picture print film |
US5689372A (en) * | 1995-12-22 | 1997-11-18 | Eastman Kodak Company | Integral imaging with anti-halation |
US5576162A (en) * | 1996-01-18 | 1996-11-19 | Eastman Kodak Company | Imaging element having an electrically-conductive layer |
EP0791858B1 (en) | 1996-02-26 | 2000-10-11 | Agfa-Gevaert N.V. | A method for making by phototypesetting a lithographic printing plate according to the silver salt diffusion transfer process |
US5747232A (en) * | 1997-02-27 | 1998-05-05 | Eastman Kodak Company | Motion imaging film comprising a carbon black-containing backing and a process surviving conductive subbing layer |
US5786134A (en) * | 1997-05-15 | 1998-07-28 | Eastman Kodak Company | Motion picture print film |
US6096491A (en) * | 1998-10-15 | 2000-08-01 | Eastman Kodak Company | Antistatic layer for imaging element |
US6190846B1 (en) | 1998-10-15 | 2001-02-20 | Eastman Kodak Company | Abrasion resistant antistatic with electrically conducting polymer for imaging element |
EP1081546A1 (en) | 1999-08-30 | 2001-03-07 | Eastman Kodak Company | Coating composition containing electrically-conductive polymer and solvent mixture |
US6162596A (en) * | 1999-08-30 | 2000-12-19 | Eastman Kodak Company | Imaging elements containing an electrically-conductive layer comprising polythiophene and a cellulosic polymer binder |
US20050029496A1 (en) * | 2001-06-26 | 2005-02-10 | Schwark Dwight W. | Coating composition containing polythiophene, film-forming binder, and solvent mixture |
US20040135126A1 (en) * | 2001-06-26 | 2004-07-15 | Schwark Dwight W. | Coating composition containing polythiophene and solvent mixture |
-
1940
- 1940-09-16 GB GB14235/40A patent/GB544006A/en not_active Expired
-
1941
- 1941-03-26 US US385277A patent/US2327828A/en not_active Expired - Lifetime
- 1941-08-30 DE DEK2577D patent/DE893009C/en not_active Expired
-
1945
- 1945-08-02 FR FR937743D patent/FR937743A/en not_active Expired
- 1945-08-03 FR FR945157D patent/FR945157A/en not_active Expired
-
1947
- 1947-12-29 FR FR57920D patent/FR57920E/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
DE893009C (en) | 1953-10-12 |
FR945157A (en) | 1949-04-27 |
FR57920E (en) | 1953-09-18 |
US2327828A (en) | 1943-08-24 |
FR937743A (en) | 1948-08-25 |
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