GB1138551A - Electrophotographic material - Google Patents

Electrophotographic material

Info

Publication number
GB1138551A
GB1138551A GB2196/66A GB219666A GB1138551A GB 1138551 A GB1138551 A GB 1138551A GB 2196/66 A GB2196/66 A GB 2196/66A GB 219666 A GB219666 A GB 219666A GB 1138551 A GB1138551 A GB 1138551A
Authority
GB
United Kingdom
Prior art keywords
phenol
resin
formaldehyde
integer
jan
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
Application number
GB2196/66A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Xerox Ltd
Original Assignee
Rank Xerox Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Rank Xerox Ltd filed Critical Rank Xerox Ltd
Publication of GB1138551A publication Critical patent/GB1138551A/en
Expired legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G5/00Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
    • G03G5/02Charge-receiving layers
    • G03G5/04Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
    • G03G5/06Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
    • G03G5/07Polymeric photoconductive materials
    • G03G5/075Polymeric photoconductive materials obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G5/00Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
    • G03G5/02Charge-receiving layers
    • G03G5/04Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
    • G03G5/06Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
    • G03G5/07Polymeric photoconductive materials
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S430/00Radiation imagery chemistry: process, composition, or product thereof
    • Y10S430/001Electric or magnetic imagery, e.g., xerography, electrography, magnetography, etc. Process, composition, or product
    • Y10S430/10Donor-acceptor complex photoconductor

Landscapes

  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Photoreceptors In Electrophotography (AREA)

Abstract

1,138,551. Phenolic-resin composition. RANK XEROX Ltd. 17 Jan., 1966 [18 Jan., 1965], No. 2196/66. Heading C3R. [Also in Division H1] The invention comprises a charge-transfer complex of a phenol-aldehyde resin and a Lewis acid. Preferably the resin has the formula where R is a residue selected from formaldehyde, paraformaldehyde, furfural, amino formaldehyde, acrolein, benzaldehyde, chloral, oxoaldehydes, acetaldehyde, glyoxal, propionaldehyde, n-butyraldehyde, isobutyraldehyde, nvaleraldehyde, isovaleraldehyde, n-coproaldehyde, n-heptaldehyde, stearaldehyde and crotonaldehyde or mixtures thereof; Y is H, OH, halogen or lower alkyl X is O or R Z is an integer of at least 2 n is an integer up to 4 and m is an integer up to 3. In the examples the resins used are a dimethyl diphenyl oxide-phenol resin modified with diphenyl oxide, rosin modified phenolformaldehyde, phenol-formaldehyde and pphenyl phenol-formaldehyde whilst the Lewis acids used are 2,4,7-trinitrofluorenone, benzophenone tetracarboxylic acid, benzanthracene- 7,12-dione, aurintricarboxylic acid, 1,3,5-trinitrobenzene, 2,3-dichloro-1 ,4-naphthaquinone. Ethyl methacrylate resin may be used as a binder together with sensitizers such as pyronin B, methylene green, brilliant green and eosine Y. Numerous other Lewis acids of the organic and the inorganic types are specified. Also listed are phenols which may be used to form the phenol-aldehyde resin. The photoconductive material may be coated on Al foil to form an electrophotographic plate or may be used as a self-supporting transparent sheet.
GB2196/66A 1965-01-18 1966-01-17 Electrophotographic material Expired GB1138551A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US426409A US3408183A (en) 1965-01-18 1965-01-18 Electrophotographic materials and methods employing photoconductive resinous charge transfer complexes

Publications (1)

Publication Number Publication Date
GB1138551A true GB1138551A (en) 1969-01-01

Family

ID=23690694

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2196/66A Expired GB1138551A (en) 1965-01-18 1966-01-17 Electrophotographic material

Country Status (4)

Country Link
US (1) US3408183A (en)
DE (1) DE1522676C3 (en)
FR (1) FR1463745A (en)
GB (1) GB1138551A (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3561358A (en) * 1966-10-10 1971-02-09 Xerox Corp Gravure imaging system
US3655378A (en) * 1971-03-01 1972-04-11 Eastman Kodak Co Charge-transfer complexes of dibenzofuran-formaldehyde or dibenzothiophene-formaldehyde resins as photoconductive materials
US3778841A (en) * 1972-08-09 1973-12-11 Xerox Corp Induction imaging system
US4105447A (en) * 1975-07-14 1978-08-08 Eastman Kodak Company Photoconductive insulating compositions including polyaryl hydrocarbon photoconductors
GB1570519A (en) * 1975-11-11 1980-07-02 Ricoh Kk Electrophotographic light-sensitive members
JPS57147656A (en) * 1981-03-09 1982-09-11 Fuji Photo Film Co Ltd Electrophotographic sensitive printing plate material

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2319142A (en) * 1941-01-17 1943-05-11 Haveg Corp Method of preparing phenolic resin compositions
US2655490A (en) * 1950-06-03 1953-10-13 Dow Chemical Co Catalytic hardening of phenol-formaldehyde resins and compositions comprising same
BE570790A (en) * 1957-09-07
US3056754A (en) * 1958-09-03 1962-10-02 Albert Ag Chem Werke Vulcanizable composition comprising rubber and a resinous complex reaction product of a phenol-formaldehyde condensate and a metal chloride, and process for vulcanizing same
US3300419A (en) * 1963-07-15 1967-01-24 Evans Prod Co Phenolic resin cellular materials and method for making same

Also Published As

Publication number Publication date
DE1522676B2 (en) 1975-03-20
US3408183A (en) 1968-10-29
DE1522676A1 (en) 1969-10-16
DE1522676C3 (en) 1975-10-30
FR1463745A (en) 1966-06-03

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