DE3413833A1 - Entwicklungsverfahren und entwickler dafuer - Google Patents
Entwicklungsverfahren und entwickler dafuerInfo
- Publication number
- DE3413833A1 DE3413833A1 DE19843413833 DE3413833A DE3413833A1 DE 3413833 A1 DE3413833 A1 DE 3413833A1 DE 19843413833 DE19843413833 DE 19843413833 DE 3413833 A DE3413833 A DE 3413833A DE 3413833 A1 DE3413833 A1 DE 3413833A1
- Authority
- DE
- Germany
- Prior art keywords
- developer
- toner
- nitrogen
- development
- charge image
- 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.)
- Granted
Links
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- 238000011161 development Methods 0.000 title claims description 73
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 69
- -1 nitrogen-containing compound Chemical class 0.000 claims description 57
- 239000002245 particle Substances 0.000 claims description 35
- 239000000377 silicon dioxide Substances 0.000 claims description 27
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 21
- 150000001875 compounds Chemical class 0.000 claims description 18
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 16
- 125000000623 heterocyclic group Chemical group 0.000 claims description 16
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- 229960000228 cetalkonium chloride Drugs 0.000 description 2
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- RIFHJAODNHLCBH-UHFFFAOYSA-N methanethione Chemical group S=[CH] RIFHJAODNHLCBH-UHFFFAOYSA-N 0.000 description 1
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- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
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- 229920001490 poly(butyl methacrylate) polymer Polymers 0.000 description 1
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- 230000000717 retained effect Effects 0.000 description 1
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- OARRHUQTFTUEOS-UHFFFAOYSA-N safranin Chemical compound [Cl-].C=12C=C(N)C(C)=CC2=NC2=CC(C)=C(N)C=C2[N+]=1C1=CC=CC=C1 OARRHUQTFTUEOS-UHFFFAOYSA-N 0.000 description 1
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- 125000006850 spacer group Chemical group 0.000 description 1
- 125000003696 stearoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
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- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
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- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000002813 thiocarbonyl group Chemical group *C(*)=S 0.000 description 1
- 125000000464 thioxo group Chemical group S=* 0.000 description 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
- 125000005425 toluyl group Chemical group 0.000 description 1
- PZJJKWKADRNWSW-UHFFFAOYSA-N trimethoxysilicon Chemical group CO[Si](OC)OC PZJJKWKADRNWSW-UHFFFAOYSA-N 0.000 description 1
- KHOQXNHADJBILQ-UHFFFAOYSA-N trimethyl(sulfanyl)silane Chemical compound C[Si](C)(C)S KHOQXNHADJBILQ-UHFFFAOYSA-N 0.000 description 1
- 239000005051 trimethylchlorosilane Substances 0.000 description 1
- PQDJYEQOELDLCP-UHFFFAOYSA-N trimethylsilane Chemical compound C[SiH](C)C PQDJYEQOELDLCP-UHFFFAOYSA-N 0.000 description 1
- 125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
- 125000003774 valeryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N vinyl ethyl ether Natural products CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 1
- JLIDVCMBCGBIEY-UHFFFAOYSA-N vinyl ethyl ketone Natural products CCC(=O)C=C JLIDVCMBCGBIEY-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000012800 visualization Methods 0.000 description 1
- 235000014101 wine Nutrition 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
- G03G9/097—Plasticisers; Charge controlling agents
- G03G9/09733—Organic compounds
- G03G9/09758—Organic compounds comprising a heterocyclic ring
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G13/00—Electrographic processes using a charge pattern
- G03G13/06—Developing
- G03G13/08—Developing using a solid developer, e.g. powder developer
-
- 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
- G03G9/09—Colouring agents for toner particles
- G03G9/0906—Organic dyes
- G03G9/0918—Phthalocyanine dyes
-
- 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
- G03G9/097—Plasticisers; Charge controlling agents
- G03G9/09708—Inorganic compounds
- G03G9/09716—Inorganic compounds treated with organic compounds
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
- Y10T428/2991—Coated
- Y10T428/2993—Silicic or refractory material containing [e.g., tungsten oxide, glass, cement, etc.]
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Developing Agents For Electrophotography (AREA)
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58063935A JPS59189352A (ja) | 1983-04-12 | 1983-04-12 | 正帯電性現像剤 |
JP58096512A JPS59222849A (ja) | 1983-05-31 | 1983-05-31 | 現像方法 |
JP58096511A JPS59222862A (ja) | 1983-05-31 | 1983-05-31 | 現像方法 |
JP58112411A JPS603679A (ja) | 1983-06-22 | 1983-06-22 | 現像方法 |
JP58113965A JPS604953A (ja) | 1983-06-23 | 1983-06-23 | 現像方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
DE3413833A1 true DE3413833A1 (de) | 1984-10-18 |
DE3413833C2 DE3413833C2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1991-05-29 |
Family
ID=27523816
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19843413833 Granted DE3413833A1 (de) | 1983-04-12 | 1984-04-12 | Entwicklungsverfahren und entwickler dafuer |
Country Status (2)
Country | Link |
---|---|
US (1) | US4680245A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |
DE (1) | DE3413833A1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3438430A1 (de) * | 1983-10-19 | 1985-05-02 | Canon K.K., Tokio/Tokyo | Entwicklungsverfahren |
Families Citing this family (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3604827A1 (de) * | 1986-02-15 | 1987-08-20 | Bayer Ag | Elektrophotographische toner |
US4833059A (en) * | 1986-03-18 | 1989-05-23 | Kabushiki Kaisha Toshiba | Developing method using one-component non-magnetic toner with positive frictional charge |
DE3707262A1 (de) * | 1987-03-06 | 1988-09-15 | Bayer Ag | Methinfanalpigmente enthaltende trockentoner |
US4935325A (en) * | 1987-09-10 | 1990-06-19 | Canon Kabushiki Kaisha | Toner and image forming method using magnetic material with specific tap density and linseed oil absorption |
JP2729301B2 (ja) * | 1988-06-24 | 1998-03-18 | コニカ株式会社 | 電子写真画像形成方法 |
US4902598A (en) * | 1988-07-01 | 1990-02-20 | Xerox Corporation | Process for the preparation of silica containing charge enhancing additives |
US5307122A (en) * | 1989-07-28 | 1994-04-26 | Canon Kabushiki Kaisha | Image forming apparatus apparatus unit facsimile apparatus and developer comprising hydrophobic silica fine powder for developing electrostatic images |
JP2623938B2 (ja) * | 1990-08-21 | 1997-06-25 | 富士ゼロックス株式会社 | 電子写真用トナー |
JP2623945B2 (ja) * | 1990-09-17 | 1997-06-25 | 富士ゼロックス株式会社 | 電子写真用トナー |
US5306588A (en) * | 1991-03-19 | 1994-04-26 | Canon Kabushiki Kaisha | Treated silica fine powder and toner for developing electrostatic images |
US5202209A (en) * | 1991-10-25 | 1993-04-13 | Xerox Corporation | Toner and developer compositions with surface additives |
US5288580A (en) * | 1991-12-23 | 1994-02-22 | Xerox Corporation | Toner and processes thereof |
JPH06336049A (ja) * | 1993-05-31 | 1994-12-06 | Brother Ind Ltd | 画像形成装置 |
US5953570A (en) * | 1996-10-25 | 1999-09-14 | Minolta Co., Ltd. | Developing device for an image forming apparatus |
US5989768A (en) * | 1997-03-06 | 1999-11-23 | Cabot Corporation | Charge-modified metal oxides with cyclic silazane and electrostatographic systems incorporating same |
US6245839B1 (en) | 1998-11-25 | 2001-06-12 | The Lubrizol Corporation | Powder-coating compositions containing transfer efficiency-enhancing additives |
GB2373789B (en) * | 2001-03-31 | 2004-06-09 | Ilford Imaging Uk Ltd | Polycyclic chromophoric systems substituted by (oxo-pyrazolyl) methyl radicals |
US6605402B2 (en) | 2001-08-21 | 2003-08-12 | Aetas Technology, Incorporated | Method of using variably sized coating particles in a mono component developing system |
US7169208B2 (en) * | 2004-06-10 | 2007-01-30 | Inco Limited | Method and composition for dispersing extra-fine nickel powder |
KR101172449B1 (ko) * | 2005-02-15 | 2012-08-07 | 엘지전자 주식회사 | 전자 종이 표시 장치용 입자 및 그 제조 방법 |
JP7000737B2 (ja) * | 2017-08-22 | 2022-01-19 | コニカミノルタ株式会社 | 現像装置および画像形成装置 |
JP7330725B2 (ja) * | 2019-03-19 | 2023-08-22 | キヤノン株式会社 | トナー用外添剤及びトナー |
CN118290801B (zh) * | 2024-04-03 | 2024-11-29 | 未来创建(深圳)科技有限公司 | 一种高耐磨类纸膜及其制备方法和应用 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2606749B2 (de) * | 1975-02-21 | 1978-07-06 | Kanebo, Ltd., Tokio | Toner für elektrophotographische Entwickler |
DE3142974A1 (de) * | 1980-10-31 | 1982-06-03 | Canon K.K., Tokyo | Entwickler fuer elektrophotographische zwecke und entwicklungsverfahren |
DE3330380A1 (de) * | 1982-08-23 | 1984-02-23 | Canon K.K., Tokyo | Entwickler und entwicklungsverfahren |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3229419A (en) * | 1959-06-04 | 1966-01-18 | Fry Carroll Brooks | Cartesian diving element for cartesian toys |
GB1086753A (en) * | 1964-02-06 | 1967-10-11 | Dennison Mfg Ltd | Development of electrostatic images with liquid developer |
US3526533A (en) * | 1966-08-10 | 1970-09-01 | Xerox Corp | Coated carrier particles |
US3551337A (en) * | 1967-09-01 | 1970-12-29 | Eastman Kodak Co | Liquid developers for electrostatic images |
US3542681A (en) * | 1968-07-10 | 1970-11-24 | Gaf Corp | Negative working electrostatic toners |
NL7508056A (nl) * | 1975-07-07 | 1977-01-11 | Oce Van Der Grinten Nv | Tonerpoeder voor het ontwikkelen van elektro- statische beelden. |
JPS55126266A (en) * | 1979-03-23 | 1980-09-29 | Hitachi Metals Ltd | Electrophotographic method |
JPS55118050A (en) * | 1979-03-06 | 1980-09-10 | Canon Inc | Method and apparatus for developing |
JPS5692545A (en) * | 1979-12-26 | 1981-07-27 | Minolta Camera Co Ltd | Electrophotographic developing agent and developing method |
-
1984
- 1984-04-12 DE DE19843413833 patent/DE3413833A1/de active Granted
-
1986
- 1986-11-12 US US06/929,495 patent/US4680245A/en not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2606749B2 (de) * | 1975-02-21 | 1978-07-06 | Kanebo, Ltd., Tokio | Toner für elektrophotographische Entwickler |
DE3142974A1 (de) * | 1980-10-31 | 1982-06-03 | Canon K.K., Tokyo | Entwickler fuer elektrophotographische zwecke und entwicklungsverfahren |
DE3330380A1 (de) * | 1982-08-23 | 1984-02-23 | Canon K.K., Tokyo | Entwickler und entwicklungsverfahren |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3438430A1 (de) * | 1983-10-19 | 1985-05-02 | Canon K.K., Tokio/Tokyo | Entwicklungsverfahren |
Also Published As
Publication number | Publication date |
---|---|
US4680245A (en) | 1987-07-14 |
DE3413833C2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1991-05-29 |
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