CA1140785A - Composition pour revelateur renfermant du noir actif et un copolymere de chlorure de vinyle, avec du maleate d'ethyle, de propyle ou de butyle - Google Patents

Composition pour revelateur renfermant du noir actif et un copolymere de chlorure de vinyle, avec du maleate d'ethyle, de propyle ou de butyle

Info

Publication number: CA1140785A
Authority: CA; Canada
Prior art keywords: particles; toner; weight; copolymer; resin
Prior art date: 1979-07-02
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

CA000351553A

Other languages

English (en)

Inventor

Steven B. Bolte

John F. Knapp

Dale R. Ims

Richard B. Lewis

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 Corp

Original Assignee

Xerox Corp

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.)

1979-07-02

Filing date

1980-05-09

Publication date

1983-02-08

1980-05-09 Application filed by Xerox Corp filed Critical Xerox Corp

1983-02-08 Application granted granted Critical

1983-02-08 Publication of CA1140785A publication Critical patent/CA1140785A/fr

Status Expired legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 24
229920001577 copolymer Polymers 0.000 title claims abstract description 15
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 title claims abstract description 9
239000006229 carbon black Substances 0.000 title claims description 7
UTOVMEACOLCUCK-PLNGDYQASA-N butyl maleate Chemical compound CCCCOC(=O)\C=C/C(O)=O UTOVMEACOLCUCK-PLNGDYQASA-N 0.000 title claims 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 title description 2
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 title description 2
239000003086 colorant Substances 0.000 claims abstract description 12
239000002245 particle Substances 0.000 claims description 78
229920005989 resin Polymers 0.000 claims description 32
239000011347 resin Substances 0.000 claims description 32
IEPRKVQEAMIZSS-UHFFFAOYSA-N Di-Et ester-Fumaric acid Natural products CCOC(=O)C=CC(=O)OCC IEPRKVQEAMIZSS-UHFFFAOYSA-N 0.000 claims description 6
IEPRKVQEAMIZSS-WAYWQWQTSA-N Diethyl maleate Chemical compound CCOC(=O)\C=C/C(=O)OCC IEPRKVQEAMIZSS-WAYWQWQTSA-N 0.000 claims description 6
229920006026 co-polymeric resin Polymers 0.000 claims description 3
DSTWFRCNXMNXTR-WAYWQWQTSA-N dipropyl (z)-but-2-enedioate Chemical compound CCCOC(=O)\C=C/C(=O)OCCC DSTWFRCNXMNXTR-WAYWQWQTSA-N 0.000 claims description 2
239000004615 ingredient Substances 0.000 claims 1
-1 alkyl maleate Chemical compound 0.000 abstract description 6
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 abstract description 6
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 abstract description 3
239000011521 glass Substances 0.000 description 13
238000000034 method Methods 0.000 description 13
238000012360 testing method Methods 0.000 description 11
239000011324 bead Substances 0.000 description 9
229920000642 polymer Polymers 0.000 description 7
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 6
238000011161 development Methods 0.000 description 6
230000018109 developmental process Effects 0.000 description 6
230000009477 glass transition Effects 0.000 description 6
239000000463 material Substances 0.000 description 6
239000000178 monomer Substances 0.000 description 6
239000000843 powder Substances 0.000 description 6
239000007921 spray Substances 0.000 description 6
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 5
238000002360 preparation method Methods 0.000 description 5
230000009467 reduction Effects 0.000 description 5
238000006722 reduction reaction Methods 0.000 description 5
239000012260 resinous material Substances 0.000 description 5
238000001694 spray drying Methods 0.000 description 5
229910000859 α-Fe Inorganic materials 0.000 description 5
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
239000000969 carrier Substances 0.000 description 4
239000000975 dye Substances 0.000 description 4
238000010951 particle size reduction Methods 0.000 description 4
230000008569 process Effects 0.000 description 4
238000005549 size reduction Methods 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
230000000903 blocking effect Effects 0.000 description 3
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
239000012876 carrier material Substances 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
239000011248 coating agent Substances 0.000 description 3
238000000576 coating method Methods 0.000 description 3
JBSLOWBPDRZSMB-FPLPWBNLSA-N dibutyl (z)-but-2-enedioate Chemical compound CCCCOC(=O)\C=C/C(=O)OCCCC JBSLOWBPDRZSMB-FPLPWBNLSA-N 0.000 description 3
230000005291 magnetic effect Effects 0.000 description 3
239000000049 pigment Substances 0.000 description 3
238000005096 rolling process Methods 0.000 description 3
239000002904 solvent Substances 0.000 description 3
230000000007 visual effect Effects 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
UWNADWZGEHDQAB-UHFFFAOYSA-N 2,5-dimethylhexane Chemical group CC(C)CCC(C)C UWNADWZGEHDQAB-UHFFFAOYSA-N 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 2
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
208000036366 Sensation of pressure Diseases 0.000 description 2
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
230000009471 action Effects 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
229910052742 iron Inorganic materials 0.000 description 2
238000005259 measurement Methods 0.000 description 2
238000002156 mixing Methods 0.000 description 2
229910052759 nickel Inorganic materials 0.000 description 2
235000012771 pancakes Nutrition 0.000 description 2
229920003023 plastic Polymers 0.000 description 2
239000004033 plastic Substances 0.000 description 2
229920005990 polystyrene resin Polymers 0.000 description 2
238000003860 storage Methods 0.000 description 2
229920002554 vinyl polymer Polymers 0.000 description 2
230000004580 weight loss Effects 0.000 description 2
UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 1
ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 2,3-dimethylbutane Chemical group CC(C)C(C)C ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 0.000 description 1
229910002012 Aerosil® Inorganic materials 0.000 description 1
239000004342 Benzoyl peroxide Substances 0.000 description 1
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
229910001369 Brass Inorganic materials 0.000 description 1
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
239000002033 PVDF binder Substances 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
239000004372 Polyvinyl alcohol Substances 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
239000006230 acetylene black Substances 0.000 description 1
238000013019 agitation Methods 0.000 description 1
229940072049 amyl acetate Drugs 0.000 description 1
PGMYKACGEOXYJE-UHFFFAOYSA-N anhydrous amyl acetate Natural products CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 1
239000012736 aqueous medium Substances 0.000 description 1
239000003849 aromatic solvent Substances 0.000 description 1
IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 description 1
230000008901 benefit Effects 0.000 description 1
235000019400 benzoyl peroxide Nutrition 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
239000010951 brass Substances 0.000 description 1
239000003990 capacitor Substances 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
239000012986 chain transfer agent Substances 0.000 description 1
230000008859 change Effects 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical group FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 description 1
239000010941 cobalt Substances 0.000 description 1
229910017052 cobalt Inorganic materials 0.000 description 1
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
239000008119 colloidal silica Substances 0.000 description 1
238000004040 coloring Methods 0.000 description 1
238000007334 copolymerization reaction Methods 0.000 description 1
XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
229920006037 cross link polymer Polymers 0.000 description 1
239000003431 cross linking reagent Substances 0.000 description 1
235000013365 dairy product Nutrition 0.000 description 1
125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
238000001035 drying Methods 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
229940093499 ethyl acetate Drugs 0.000 description 1
235000019439 ethyl acetate Nutrition 0.000 description 1
239000003302 ferromagnetic material Substances 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
229910021485 fumed silica Inorganic materials 0.000 description 1
238000005227 gel permeation chromatography Methods 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 description 1
230000002209 hydrophobic effect Effects 0.000 description 1
238000003384 imaging method Methods 0.000 description 1
230000002452 interceptive effect Effects 0.000 description 1
SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000006233 lamp black Substances 0.000 description 1
239000004816 latex Substances 0.000 description 1
229920000126 latex Polymers 0.000 description 1
MOUPNEIJQCETIW-UHFFFAOYSA-N lead chromate Chemical compound [Pb+2].[O-][Cr]([O-])(=O)=O MOUPNEIJQCETIW-UHFFFAOYSA-N 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000000696 magnetic material Substances 0.000 description 1
239000006249 magnetic particle Substances 0.000 description 1
229940107698 malachite green Drugs 0.000 description 1
FDZZZRQASAIRJF-UHFFFAOYSA-M malachite green Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1C(C=1C=CC=CC=1)=C1C=CC(=[N+](C)C)C=C1 FDZZZRQASAIRJF-UHFFFAOYSA-M 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
CXKWCBBOMKCUKX-UHFFFAOYSA-M methylene blue Chemical compound [Cl-].C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 CXKWCBBOMKCUKX-UHFFFAOYSA-M 0.000 description 1
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical group CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 1
TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 1
229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920000515 polycarbonate Polymers 0.000 description 1
239000004417 polycarbonate Substances 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
239000004926 polymethyl methacrylate Substances 0.000 description 1
229920000098 polyolefin Polymers 0.000 description 1
229920001343 polytetrafluoroethylene Polymers 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
229920002981 polyvinylidene fluoride Polymers 0.000 description 1
238000010298 pulverizing process Methods 0.000 description 1
229940051201 quinoline yellow Drugs 0.000 description 1
239000004172 quinoline yellow Substances 0.000 description 1
IZMJMCDDWKSTTK-UHFFFAOYSA-N quinoline yellow Chemical compound C1=CC=CC2=NC(C3C(C4=CC=CC=C4C3=O)=O)=CC=C21 IZMJMCDDWKSTTK-UHFFFAOYSA-N 0.000 description 1
235000012752 quinoline yellow Nutrition 0.000 description 1
238000011084 recovery Methods 0.000 description 1
239000004576 sand Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000004575 stone Substances 0.000 description 1
239000000758 substrate Substances 0.000 description 1
238000007864 suspending Methods 0.000 description 1
238000010557 suspension polymerization reaction Methods 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
235000013799 ultramarine blue Nutrition 0.000 description 1
229920006163 vinyl copolymer Polymers 0.000 description 1
XOSXWYQMOYSSKB-LDKJGXKFSA-L water blue Chemical compound CC1=CC(/C(\C(C=C2)=CC=C2NC(C=C2)=CC=C2S([O-])(=O)=O)=C(\C=C2)/C=C/C\2=N\C(C=C2)=CC=C2S([O-])(=O)=O)=CC(S(O)(=O)=O)=C1N.[Na+].[Na+] XOSXWYQMOYSSKB-LDKJGXKFSA-L 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/087—Binders for toner particles
- G03G9/08702—Binders for toner particles comprising macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- G03G9/08726—Polymers of unsaturated acids or derivatives thereof
- G03G9/08731—Polymers of nitriles
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/087—Binders for toner particles
- G03G9/08702—Binders for toner particles comprising macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- G03G9/08713—Polyvinylhalogenides
- G03G9/08715—Polyvinylhalogenides containing chlorine, bromine or iodine
- G03G9/08717—Polyvinylchloride

Landscapes

Physics & Mathematics (AREA)
Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Spectroscopy & Molecular Physics (AREA)
General Physics & Mathematics (AREA)
Developing Agents For Electrophotography (AREA)

CA000351553A 1979-07-02 1980-05-09 Composition pour revelateur renfermant du noir actif et un copolymere de chlorure de vinyle, avec du maleate d'ethyle, de propyle ou de butyle Expired CA1140785A (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US5419179A	1979-07-02	1979-07-02
US054,191		1979-07-02

Publications (1)

Publication Number	Publication Date
CA1140785A true CA1140785A (fr)	1983-02-08

Family

ID=21989353

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000351553A Expired CA1140785A (fr)	1979-07-02	1980-05-09	Composition pour revelateur renfermant du noir actif et un copolymere de chlorure de vinyle, avec du maleate d'ethyle, de propyle ou de butyle

Country Status (4)

Country	Link
EP (1)	EP0022639B1 (fr)
JP (1)	JPS5612649A (fr)
CA (1)	CA1140785A (fr)
ES (1)	ES493003A0 (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS60229035A (ja) *	1984-04-27	1985-11-14	Canon Inc	現像方法
WO2016195436A1 (fr) *	2015-06-05	2016-12-08	주식회사 엘지화학	Polymère à base de chlorure de vinyle, procédé de préparation correspondant et composition de résine thermoplastique le comprenant

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5123354B2 (fr) *	1973-01-16	1976-07-16

1980
- 1980-05-09 CA CA000351553A patent/CA1140785A/fr not_active Expired
- 1980-06-30 JP JP8905080A patent/JPS5612649A/ja active Pending
- 1980-07-01 ES ES493003A patent/ES493003A0/es active Granted
- 1980-07-02 EP EP19800302229 patent/EP0022639B1/fr not_active Expired

Also Published As

Publication number	Publication date
EP0022639A1 (fr)	1981-01-21
ES8105487A1 (es)	1981-06-01
ES493003A0 (es)	1981-06-01
EP0022639B1 (fr)	1983-05-25
JPS5612649A (en)	1981-02-07

Legal Events

Date	Code	Title	Description
2000-02-08	MKEX	Expiry

Publication	Publication Date	Title
US4621039A (en)	1986-11-04	Developer compositions with fast admixing characteristics
CA1112499A (fr)	1981-11-17	Methode de fabrication de toner par polymerisation et attrition a nombre d'operations reduit
US5470687A (en)	1995-11-28	Process for producing toner particles using free space formed in a polymeric medium
DE19546757A1 (de)	1996-06-20	Verkapselter Toner zur Wärme-und-Druck-Fixierung
US4791041A (en)	1988-12-13	Magnetic carrier particles for electrophotographic developer
US5622802A (en)	1997-04-22	Toner for electrostatic latent image developing
US6057409A (en)	2000-05-02	Supercritical polymerization processes
JPH0519536A (ja)	1993-01-29	静電荷像現像用カラートナーの組合せ
DE69426512T2 (de)	2001-06-13	Kapseltoner zur Wärme-und-Druck-Fixierung und Verfahren zu dessen Herstellung
US7183030B2 (en)	2007-02-27	Negatively charged coated electrographic toner particles and process
JP3600790B2 (ja)	2004-12-15	靜電潜像現像用カラートナー、および靜電潜像現像用カラートナーの製造方法
US5178984A (en)	1993-01-12	Electrophotographic toner
US5514512A (en)	1996-05-07	Method of making coated carrier particles
CA1140785A (fr)	1983-02-08	Composition pour revelateur renfermant du noir actif et un copolymere de chlorure de vinyle, avec du maleate d'ethyle, de propyle ou de butyle
US5516618A (en)	1996-05-14	Method of making carriers having coatings with fillers
US5731121A (en)	1998-03-24	Developer for electrostatic latent image development
EP0034423A1 (fr)	1981-08-26	Procédé de fabrication de particules véhiculatrices revêtues pour des mélanges de développement électrostatographique
US5514513A (en)	1996-05-07	Method of making coated carrier particles
KR100636160B1 (ko)	2006-10-18	양으로 대전 코팅된 전자기록 토너 입자
US5380615A (en)	1995-01-10	Process for producing a toner for development of electrostatic charged image
US7183031B2 (en)	2007-02-27	Positively charged coated electrographic toner particles
CA1140786A (fr)	1983-02-08	Melange aviveur de ton, a base d'epoxy esterifie et de resines phenoxy esterifiees
CA1117349A (fr)	1982-02-02	Particule de support, avec revetement externe en terpolymere de chlorure de vinyle et d'acetate de vinyle, contenant de l'alcool vinylique ou un acide dibasique
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JPS6239878A (ja)	1987-02-20	現像剤