GB1181287A - Developer for Electrophotography - Google Patents

Developer for Electrophotography

Info

Publication number
GB1181287A
GB1181287A GB2616767A GB2616767A GB1181287A GB 1181287 A GB1181287 A GB 1181287A GB 2616767 A GB2616767 A GB 2616767A GB 2616767 A GB2616767 A GB 2616767A GB 1181287 A GB1181287 A GB 1181287A
Authority
GB
United Kingdom
Prior art keywords
methacrylate
diazotized
dye
acrylamide
copper phthalocyanine
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
GB2616767A
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.)
DAINICHSEIKA KOGYO KABUSHIKI K
Canon Inc
Original Assignee
DAINICHSEIKA KOGYO KABUSHIKI K
Canon Camera Co Inc
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 DAINICHSEIKA KOGYO KABUSHIKI K, Canon Camera Co Inc filed Critical DAINICHSEIKA KOGYO KABUSHIKI K
Publication of GB1181287A publication Critical patent/GB1181287A/en
Expired legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00Developers
    • G03G9/08Developers with toner particles
    • G03G9/087Binders for toner particles
    • G03G9/08784Macromolecular material not specially provided for in a single one of groups G03G9/08702 - G03G9/08775
    • G03G9/08791Macromolecular material not specially provided for in a single one of groups G03G9/08702 - G03G9/08775 characterised by the presence of specified groups or side chains
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00Developers
    • G03G9/08Developers with toner particles
    • G03G9/09Colouring agents for toner particles
    • G03G9/0906Organic dyes

Landscapes

  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Liquid Developers In Electrophotography (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

1,181,287. Coloured addition polymers. CANON CAMERA CO. Inc., DAINICHISEIKA KOGYO K.K., and E. INOUE. 6 June, 1967 [6 June, 1966], No. 26167/67. Heading C3P. [Also in Division G2] Coloured polymers comprising a polymer chain having a coloured molecule chemically bonded thereto are made by copolymerizing an ethylenically unsaturated monomer or monomers either (i) together with a diazonium salt of a dye or dye intermediate or (ii) with a dye or dye intermediate containing ethylenically unsaturated groups. When a dye intermediate is used, the polymer is then treated to form the dye. The monomers preferably contain radicals which can carry a positive or negative electric charge, e.g. carboxyl, phenolic hydroxyl, sulphate ester, amino and quaternary ammonium radicals. A list of monomers and dyes is given. In examples the following dye or dye interrnediate diazonium salts and monomers are polymerized:-(1), diazotized triamino copper phthalocyanine with ethyl methacrylate, butyl acrylate, 2-dimethylaminoethyl methacrylate in the presence of polyethyleneglycol nonyl phenyl ether; (2) the zinc chloride salt of diazotized diamino copper phthalocyanine with butyl methacrylate and 2-diethylaminoethyl methacrylate in the presence of polyethylene glycol nonyl phenyl ether; (7) diazotized triamino copper phthalocyanine and acrylamide, methyl acrylate and acrylic acid;. (8) copper phthalocyanine tetra-(diazonium chloride) and methyl methacrylate, acrylamide and 2-dimethylaminoethyl methacrylate; (9) tetrachloro copper phthalocyanine tetra(diazonium chloride) and acrylamide and itaconic acid; diazotized 2: 4: 6- tris - [4 - (p - aminobenzoylamino) - 1 - anthraquinonylamino] - s - triazine stabilized with triethanolamine dodecylbenzene sulphonate and (3) polyvinyl alcohol and ethyl acrylate in the presence of dodecyl mercaptan, (5) ethyl methacrylate, octyl acrylate, 2-dimethylaminoethyl methacrylate, polyvinyl alcohol and dodecyl mercaptan, and (6) ethyl methacrylate, dibutyl itaconate, dimethylaminoethyl methacrylate, dodecyl mercaptan and FeSO 4 ; (4) diazotized diamino - perylene - tetracarboxylic acid bis - (3: 5-dimethylphenylimide) and butyl methacrylate, ethyl acrylate, acrylonitrile, glycidyl methacrylate, acrylic acid and polyethylene glycol nonyl phenyl ether; (10), diazotized 3- hydroxy-2-naphthoic acid 3<SP>1</SP>-amino-anilide and acrylamide, 2 - dimethylaminoethyl methacrylate, 2 - vinyl - 5 - methylpyridine and TiCl 3 , the polymer then being reacted with diazotized 3 - amino - 4 - methoxybenzanilide to form the dye; (11) 3-hydroxy-2-naphthoic acid (3<SP>1</SP>- methacrylamido) anilide with acrylamide, 2-dimethylaminoethyl methacrylate, methyl acrylate and potassium persulphate, the polymer then being reacted with diazotized o-anisidino-5- sulphodiethylamide to form the dye; and (12) 1 - phenyl - 3 - methyl - 4 - (4<SP>1</SP>- methacrylamido - dichlorophenylazo) - pyrazol - 5 - one with acrylamide, 2-dimethylaminoethyl methacrylate, azobisisobutyronitrile and ethylene glycol monoethyl ether. In further examples, fluorescent polymers are made by polymerizing (2) diazotized diamino- 1,2-bis-(5-methylbenzoxazole) ethene with butyl methacrylate, 2 - diethylaminoethyl methacrylate, polyethylene glycol nonyl phenyl ether and TiCl 3 ; and (13) 2-(methacrylamido-anilido)- 4 - (2: 5 - dichlorobenzoylamino) - 1: 9 - pyrimidoanthrone with dodecyl methacrylate, propylene glycol monomethacrylate, styrene, crotonic acid, azobisisobutyronitrile and ethylene glycol monoethyl ether.
GB2616767A 1966-06-06 1967-06-06 Developer for Electrophotography Expired GB1181287A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3621966 1966-06-06

Publications (1)

Publication Number Publication Date
GB1181287A true GB1181287A (en) 1970-02-11

Family

ID=12463638

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2616767A Expired GB1181287A (en) 1966-06-06 1967-06-06 Developer for Electrophotography

Country Status (2)

Country Link
DE (1) DE1572337C3 (en)
GB (1) GB1181287A (en)

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3976583A (en) * 1972-12-21 1976-08-24 Hoechst Aktiengesellschaft Electrophotographic developer liquid
US4021358A (en) * 1974-07-12 1977-05-03 Konishiroku Photo Industry Co., Ltd. Toner for developing electrostatic latent images
US4070296A (en) * 1974-08-26 1978-01-24 Xerox Corporation Triboelectrically controlled covalently dyed toner materials
US4298672A (en) * 1978-06-01 1981-11-03 Xerox Corporation Toners containing alkyl pyridinium compounds and their hydrates
US4304830A (en) * 1980-01-14 1981-12-08 Xerox Corporation Toner additives
US4324851A (en) 1979-12-20 1982-04-13 Xerox Corporation Positive color toners
US4343921A (en) 1978-11-06 1982-08-10 Usm Corporation Adhesive composition
US4391890A (en) 1981-12-03 1983-07-05 Xerox Corporation Developer compositions containing alkyl pyridinium toluene sulfonates
US4396697A (en) 1981-12-03 1983-08-02 Xerox Corporation Organic sulfonate charge enhancing additives
US4778742A (en) * 1987-10-07 1988-10-18 Xerox Corporation Colored toner compositions
GB2270319A (en) * 1992-09-04 1994-03-09 Toyo Ink Mfg Co Pigment dispersing agent and its use
US5521271A (en) * 1994-09-29 1996-05-28 Minnesota Mining And Manufacturing Company Liquid toners with hydrocarbon solvents
US5530053A (en) * 1994-05-17 1996-06-25 Minnesota Mining And Manufacturing Company Liquid toners utilizing highly fluorinated solvents
US5604070A (en) * 1995-02-17 1997-02-18 Minnesota Mining And Manufacturing Company Liquid toners with hydrocarbon solvents
US20180187017A1 (en) * 2014-12-15 2018-07-05 Boe Technology Group Co., Ltd. Dye compound and method for preparing the same, colorant, photosensitive resin composition and optical filter

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT1071148B (en) * 1976-07-29 1985-04-02 Indesit TOOL AND MACHINE FOR ASSEMBLING ELECTROLYTIC CAPACITORS

Cited By (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3976583A (en) * 1972-12-21 1976-08-24 Hoechst Aktiengesellschaft Electrophotographic developer liquid
US4021358A (en) * 1974-07-12 1977-05-03 Konishiroku Photo Industry Co., Ltd. Toner for developing electrostatic latent images
US4070296A (en) * 1974-08-26 1978-01-24 Xerox Corporation Triboelectrically controlled covalently dyed toner materials
US4298672A (en) * 1978-06-01 1981-11-03 Xerox Corporation Toners containing alkyl pyridinium compounds and their hydrates
US4343921A (en) 1978-11-06 1982-08-10 Usm Corporation Adhesive composition
US4324851A (en) 1979-12-20 1982-04-13 Xerox Corporation Positive color toners
US4304830A (en) * 1980-01-14 1981-12-08 Xerox Corporation Toner additives
US4391890A (en) 1981-12-03 1983-07-05 Xerox Corporation Developer compositions containing alkyl pyridinium toluene sulfonates
US4396697A (en) 1981-12-03 1983-08-02 Xerox Corporation Organic sulfonate charge enhancing additives
US4778742A (en) * 1987-10-07 1988-10-18 Xerox Corporation Colored toner compositions
GB2270319A (en) * 1992-09-04 1994-03-09 Toyo Ink Mfg Co Pigment dispersing agent and its use
US5420187A (en) * 1992-09-04 1995-05-30 Toyo Ink Manufacturing Co., Ltd. Pigment dispersing agent and its use
GB2270319B (en) * 1992-09-04 1997-02-26 Toyo Ink Mfg Co Pigment dispersing agent and its use
US5530053A (en) * 1994-05-17 1996-06-25 Minnesota Mining And Manufacturing Company Liquid toners utilizing highly fluorinated solvents
US5530067A (en) * 1994-05-17 1996-06-25 Minnesota Mining And Manufacturing Company Liquid toners utilizing highly fluorinated solvents
US5521271A (en) * 1994-09-29 1996-05-28 Minnesota Mining And Manufacturing Company Liquid toners with hydrocarbon solvents
US5599886A (en) * 1994-09-29 1997-02-04 Minnesota Mining And Manufacturing Company Liquid toners with hydrocarbon solvents
US5663024A (en) * 1994-09-29 1997-09-02 Minnesota Mining And Manufacturing Company Liquid toners with hydrocarbon solvents
US5604070A (en) * 1995-02-17 1997-02-18 Minnesota Mining And Manufacturing Company Liquid toners with hydrocarbon solvents
US5753763A (en) * 1995-02-17 1998-05-19 Minnesota Mining And Manufacturing Company Process for preparing liquid toners with hydrocarbon solvents
US5919866A (en) * 1995-02-17 1999-07-06 Minnesota Mining And Manufacturing Company Liquid toners with hydrocarbon solvents
US20180187017A1 (en) * 2014-12-15 2018-07-05 Boe Technology Group Co., Ltd. Dye compound and method for preparing the same, colorant, photosensitive resin composition and optical filter

Also Published As

Publication number Publication date
DE1572337C3 (en) 1979-03-29
DE1572337A1 (en) 1970-02-19
DE1572337B2 (en) 1975-06-19

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