GB883782A - Composite sheet materials for electrophotography - Google Patents
Composite sheet materials for electrophotographyInfo
- Publication number
- GB883782A GB883782A GB3525357A GB3525357A GB883782A GB 883782 A GB883782 A GB 883782A GB 3525357 A GB3525357 A GB 3525357A GB 3525357 A GB3525357 A GB 3525357A GB 883782 A GB883782 A GB 883782A
- Authority
- GB
- United Kingdom
- Prior art keywords
- binder
- copolymers
- formaldehyde
- acrylonitrile
- heterocyclic
- 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
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
- G03G5/0664—Dyes
- G03G5/0666—Dyes containing a methine or polymethine group
- G03G5/0668—Dyes containing a methine or polymethine group containing only one methine or polymethine group
- G03G5/067—Dyes containing a methine or polymethine group containing only one methine or polymethine group containing hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D221/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
- C07D221/02—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
- C07D221/04—Ortho- or peri-condensed ring systems
- C07D221/06—Ring systems of three rings
- C07D221/10—Aza-phenanthrenes
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
- G03G5/0664—Dyes
- G03G5/0666—Dyes containing a methine or polymethine group
- G03G5/0672—Dyes containing a methine or polymethine group containing two or more methine or polymethine groups
- G03G5/0674—Dyes containing a methine or polymethine group containing two or more methine or polymethine groups containing hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Photoreceptors In Electrophotography (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
An electrophotographic plate comprises a paper or metal support coated with a dispersion in a resinous binder of a photoconductive condensation product of an aromatic aldehyde with a heterocyclic compound, containing at least one active methyl group, of the formula: <FORM:0883782/III/1> in which the bracketed groups are attached to the heterocyclic ring in the 2 or 4 position and in which Y represents members of a heterocyclic six membered ring to which may be fused, for example, a substituted or unsubstituted benzene or naphthalene ring, X is an acid radical, n is 0 or 1, m is 1, 2 or 3 and R represents one or more similar or different substituents from:-a halogen atom, an alkyl or aryl radical, or a nitro, amino, hydroxy, alkylamino, arylamino, alkoxy or aryloxy group. The substances, 12 examples of which are given, may be used in the cis or trans form. Any of the dye sensitizers described in Specification 811,165 may be added to the coating material which preferably contains 1 part by weight of photoconductive compound to ,3 to 2 parts binder. Suitable binders are alkyl and aryl polysiloxanes, cellulose, cellulose ethers and esters, polyvinyl chloride, polyurethanes, polyesters, polyamides and polycarbonates. The layer is deposited from a dispersion of the photoconductor formed by adding to a solution of the photoconductor and binder a solvent in which the photoconductor is insoluble and the binder soluble. Alternatively the layer is formed from an aqueous dispersion of the photoconductor and binder. Binders suitable for application in this way are melamine-formaldehyde, urea-formaldehyde, and xylene-formaldehyde resins, polymers and copolymers based on vinyl chloride, vinylidene chloride, vinyl ethers, acrylic and methacrylic esters, acrylic amides, aromatic vinyl compounds, iso-olefines, synthetic elastomers such as copolymers of styrene and butadiene, or butadiene and acrylonitrile, copolymers of dienes with a preponderant proportion of styrene or acrylonitrile or other vinyl compounds; polyamides, polyurethanes, polyesters of polycarboxylic acids and polyhydric alcohols, polycarbonates, cellulose esters and rubber. An exemplary coating composition is described. Specifications 663,849, 772,627, 775,812 and 808,485 also are referred to.ALSO:<FORM:0883782/IV (a)/1> A supported layer for use as an electrophotographic plate (see Group XXXVI) comprises, dispersed in a resinous binder, a photoconductive condensation product of an aromatic aldehyde with a heterocyclic compound, containing at least one active methyl group of the formula: <FORM:0883782/IV (a)/2> in which the bracketed groups are attached to the heterocyclic ring in the 2 or 4 position and in which Y represents members of a heterocyclic six-membered ring to which may be fused for example a substituted or unsubstituted benzene or naphthalene ring, X is an acid radical, n is 0 or 1, m is 1, 2, or 3 and R represents one or more similar or different substituents from:- a halogen atom, an alkyl or aryl radical, or a nitro, amino, hydroxy, alkylamino, arylamino, alkoxy, or aryloxy group. The substances, 12 examples of which are given, may be used in the cis or trans form. Any of the dye sensitizers described in Specification 811,165 may be added to the layer which preferably contains 1 part by weight photoconductive compound to ,3 to 2 parts binder. Suitable binders are alkyl and aryl polysiloxanes, polyvinyl chloride, polyurethanes, polyesters, polyamides, and polycarbonates, melamine-formaldehyde, urea-formaldehyde, and xylene-formaldehyde resins, polymers and copolymers based on vinyl chloride, vinylidene chloride, vinyl ethers, acrylic and methacrylic esters, acrylic amides, aromatic vinyl compounds, iso-olefines, synthetic elastomers such as copolymers of butadiene and styrene, or butadiene and acrylonitrile, copolymers of dienes with a preponderant proportion of styrene, acrylonitrile or other vinyl compounds, polyamides, polyurethanes, polyesters or polycarboxylic acids and polyhydric alcohols and polycarbonates. In the example 20 grams of the compound of the formula shown in Fig. 2 are ball milled with 2,5 grams of the copolymer of 30 parts by weight acrylonitrile and 70 parts methyl methacrylate dissolved in 1,00 cc. of formamide and deposited on a support. Specifications 633,849, 772,647, 775,812 and 808,485 also are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEA30157A DE1104823B (en) | 1956-11-14 | 1956-11-14 | Process for the production of photoconductive layers for electrophotographic processes |
Publications (1)
Publication Number | Publication Date |
---|---|
GB883782A true GB883782A (en) | 1961-12-06 |
Family
ID=6927128
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3525357A Expired GB883782A (en) | 1956-11-14 | 1957-11-12 | Composite sheet materials for electrophotography |
Country Status (3)
Country | Link |
---|---|
DE (1) | DE1104823B (en) |
FR (1) | FR1188590A (en) |
GB (1) | GB883782A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5334485A (en) * | 1991-11-05 | 1994-08-02 | The Chromaline Corporation | Acid soluble photo-resist comprising a photosensitive polymer |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL131028C (en) * | 1959-06-25 | |||
NL128039C (en) * | 1959-07-01 | 1969-08-15 | ||
NL130145C (en) * | 1959-07-03 |
-
1956
- 1956-11-14 DE DEA30157A patent/DE1104823B/en active Pending
-
1957
- 1957-11-12 GB GB3525357A patent/GB883782A/en not_active Expired
- 1957-11-14 FR FR1188590D patent/FR1188590A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5334485A (en) * | 1991-11-05 | 1994-08-02 | The Chromaline Corporation | Acid soluble photo-resist comprising a photosensitive polymer |
Also Published As
Publication number | Publication date |
---|---|
FR1188590A (en) | 1959-09-23 |
DE1104823B (en) | 1961-04-13 |
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