JPH0287158A - Binary developer - Google Patents
Binary developerInfo
- Publication number
- JPH0287158A JPH0287158A JP63238872A JP23887288A JPH0287158A JP H0287158 A JPH0287158 A JP H0287158A JP 63238872 A JP63238872 A JP 63238872A JP 23887288 A JP23887288 A JP 23887288A JP H0287158 A JPH0287158 A JP H0287158A
- Authority
- JP
- Japan
- Prior art keywords
- copolymer
- coating
- weight
- alcohol
- toner
- 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.)
- Pending
Links
- 239000011248 coating agent Substances 0.000 claims abstract description 20
- 229920001577 copolymer Polymers 0.000 claims abstract description 18
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 claims abstract description 12
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 claims abstract description 9
- MIZLGWKEZAPEFJ-UHFFFAOYSA-N 1,1,2-trifluoroethene Chemical group FC=C(F)F MIZLGWKEZAPEFJ-UHFFFAOYSA-N 0.000 claims description 9
- 239000010419 fine particle Substances 0.000 claims description 7
- 238000000576 coating method Methods 0.000 abstract description 17
- 239000000463 material Substances 0.000 abstract description 9
- 239000006249 magnetic particle Substances 0.000 abstract description 4
- 230000006866 deterioration Effects 0.000 abstract 2
- 238000010186 staining Methods 0.000 abstract 2
- 239000007771 core particle Substances 0.000 abstract 1
- 230000000630 rising effect Effects 0.000 abstract 1
- 239000011162 core material Substances 0.000 description 13
- 235000019441 ethanol Nutrition 0.000 description 9
- 239000000969 carrier Substances 0.000 description 8
- 239000002245 particle Substances 0.000 description 8
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- -1 acrylic ester Chemical class 0.000 description 6
- 238000011109 contamination Methods 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 125000005396 acrylic acid ester group Chemical group 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000007334 copolymerization reaction Methods 0.000 description 3
- 229910000859 α-Fe Inorganic materials 0.000 description 3
- BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 239000011247 coating layer Substances 0.000 description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 description 2
- 108091008695 photoreceptors Proteins 0.000 description 2
- 229920002620 polyvinyl fluoride Polymers 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 2
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- VAJVDSVGBWFCLW-UHFFFAOYSA-N 3-Phenyl-1-propanol Chemical compound OCCCC1=CC=CC=C1 VAJVDSVGBWFCLW-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 1
- DYUQAZSOFZSPHD-UHFFFAOYSA-N Phenylpropyl alcohol Natural products CCC(O)C1=CC=CC=C1 DYUQAZSOFZSPHD-UHFFFAOYSA-N 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 235000010724 Wisteria floribunda Nutrition 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 229920006222 acrylic ester polymer Polymers 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000004807 desolvation Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000006247 magnetic powder Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 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
- G03G9/083—Magnetic toner particles
-
- 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
- G03G9/10—Developers with toner particles characterised by carrier particles
- G03G9/113—Developers with toner particles characterised by carrier particles having coatings applied thereto
- G03G9/1132—Macromolecular components of coatings
- G03G9/1133—Macromolecular components of coatings obtained by reactions only involving carbon-to-carbon unsaturated bonds
- G03G9/1134—Macromolecular components of coatings obtained by reactions only involving carbon-to-carbon unsaturated bonds containing fluorine atoms
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Developing Agents For Electrophotography (AREA)
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明は、電子写真法、静電記録法において、静電潜像
の現像のために使用される現像剤に関する。更に詳細に
は、磁性コア剤と被覆樹脂層とからなり、帯電性、耐表
面汚染性、機械強度、コアと被覆層との密着性等に於い
て優れた、負帯電性キャリアと、正帯電性トナーとから
なる磁気ブラシ用二成分現像剤に関する。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a developer used for developing electrostatic latent images in electrophotography and electrostatic recording. More specifically, a negatively chargeable carrier consisting of a magnetic core agent and a coating resin layer, which has excellent chargeability, surface contamination resistance, mechanical strength, adhesion between the core and the coating layer, etc., and a positively chargeable carrier. The present invention relates to a two-component developer for magnetic brushes comprising a magnetic toner and a magnetic brush.
従来の技術
電子写真法においては、セレンをはじめとする光導電性
物質を感光体として用い、種々の手段を用いて電気的潜
像を形成し、この潜像に磁気ブラシ現像法などを利用し
てトナーを付着させ、顕像化する方式が一般的に採用さ
れている。Conventional technology In electrophotography, a photoconductive substance such as selenium is used as a photoreceptor, an electrical latent image is formed using various means, and this latent image is developed using a magnetic brush development method or the like. Generally, a method is adopted in which toner is attached to the image and visualized.
この現像工程において、トナーに適当量の正または負の
電気量を付与し、現像域へ搬送するために、キャリアと
呼ばれる担体粒子が使用される。In this development step, carrier particles called carriers are used to impart an appropriate amount of positive or negative electricity to the toner and transport it to the development area.
キャリアは一般にコートキャリアと非コートキャリアと
に大別されるが、現像剤寿命などを考慮した場合には、
前者の方が優れていることから、種々のタイプのコート
キャリアが開発され、かつ、実用化されている0例えば
フッ化ビニルポリマー類を用いたコートキャリアが開発
されている。Carriers are generally divided into coated carriers and uncoated carriers, but when considering developer life, etc.
Since the former is superior, various types of coated carriers have been developed, and coated carriers using, for example, vinyl fluoride polymers, have been developed and are in practical use.
(例えば特開昭56−113146号公報)発明が解決
しようとする課題
]−トキャリアに対して要求される特性は、種々あるが
、特に重要な特性として、適当な帯電性、耐衝撃性、耐
摩耗性、コア物質と被覆剤との良好な密着性、電荷分布
の均−性等をあげることができる。(For example, Japanese Unexamined Patent Publication No. 56-113146) Problems to be Solved by the Invention] - There are various properties required for carriers, but particularly important properties include appropriate charging properties, impact resistance, Abrasion resistance, good adhesion between the core material and coating material, uniformity of charge distribution, etc. can be improved.
上記諸要求特性を考慮するヒ、従来使用されてきたコー
トキャリアは、依然として改善すべき問題点を残してお
り、完全なものは今までのところ知られていない0例え
ば、フッ化ビニルポリマー類は、耐表面汚染性において
優れているか、コア物質との密着性において問題があり
、また、アクリル系ポリマー類は、機械的強度、コア物
質との密着性の点では満足できるものの、耐表面汚染性
及び帯電性において問題があるとされている。いずれに
しても、一長一短のある被覆材料の使用を余儀なくされ
ているのが現状である。Considering the above-mentioned required characteristics, the coated carriers that have been used in the past still have problems to be improved, and no perfect one is known to date.For example, vinyl fluoride polymers Although acrylic polymers are satisfactory in terms of mechanical strength and adhesion with the core material, they have poor surface stain resistance. It is said that there is a problem in chargeability. In any case, the current situation is that we are forced to use coating materials that have advantages and disadvantages.
この様な現状に鑑み、本発明者等は、前記従来の諸欠点
を改善すべく種々研究、検討した結果、特定の被覆材料
を使用することが、上記コートキャリアの諸要求特性の
改良において有効であることを見出だした。更に、本発
明者等は、磁性体微粒子を分散させたトナーと該キャリ
アとからなる現像剤が、画像、寿命、機内汚染などにつ
いて、著しく良好な結果を与えるこを見出だし、本発明
を完成するに至った。In view of the current situation, the inventors of the present invention have conducted various studies and examinations to improve the various drawbacks of the conventional methods, and have found that the use of a specific coating material is effective in improving the required characteristics of the coated carrier. It was found that Furthermore, the present inventors have discovered that a developer consisting of a toner in which fine magnetic particles are dispersed and the carrier gives extremely good results in terms of images, lifespan, internal contamination, etc., and has completed the present invention. I ended up doing it.
したがって、本発明の目的は、電子写真法、静電記録法
において、静電潜像の現像のために使用される新規な現
像剤を提供することにある。Therefore, an object of the present invention is to provide a novel developer used for developing electrostatic latent images in electrophotography and electrostatic recording.
本発明の他の目的は、帯電上昇速度が高く、耐表面汚染
性が良好なため、ランニング時における帯電量の低下を
起すことがなく、また、トナー中に磁性体微粒子を含む
故に、機内汚染を生じることがない現像剤を提供するこ
とにある。Another object of the present invention is that the charging speed is high and the surface contamination resistance is good, so that the charge amount does not decrease during running, and since the toner contains magnetic fine particles, it is possible to avoid contamination inside the machine. The object of the present invention is to provide a developer that does not cause
課題を解決するための手段
本発明の前記目的は、コア物質を、フッ化ビニリデンと
トリフロロエチレン又はヘキサフロロプロピレンとの共
重合体を必須成分として含有する被覆剤で被覆して形成
された負帯電キャリアと、結着樹脂中に分散された磁性
体微粒子を含有する正帯電トナーとからなる磁気ブラシ
現像用二成分現像剤によって達成される。Means for Solving the Problems The object of the present invention is to provide a negative electrode formed by coating a core material with a coating material containing as an essential component a copolymer of vinylidene fluoride and trifluoroethylene or hexafluoropropylene. This is achieved by a two-component developer for magnetic brush development consisting of a charged carrier and a positively charged toner containing fine magnetic particles dispersed in a binder resin.
以下、本発明について詳記する。The present invention will be described in detail below.
本発明において、コア物質を被覆するための被覆剤は、
フッ化ビニリデンとトリフロロエチレン又はヘキサフロ
ロプロピレンとの共重合体を必須成分として含有するこ
とが必要である。被覆剤は、フッ化ビニリデンとトリフ
ロロエチレン又はへキサフロロプロピレンとの共重合体
のみより構成されていても、十分実用に耐えうる帯電性
、成膜特性を有するものとなるが、帯電調整自由度及び
被覆剤とコアの密着性を良好にするためには、アクリル
酸エステル重合体又は共重合体、又はトリフロロモノク
ロロエチレン−塩化ビニル共重合体を併用するのが好ま
しい。フッ化ビニリデンとトリフロロエチレン又はヘキ
サフロロプロピレンとの共重合体と、アクリル酸エステ
ル重合体又はトリフロロモノクロロエチレン−塩化ビニ
ル共重合体との混合比は、重量比で通常99;1〜20
:80が適当であり、使用するトナーの帯電上昇速度及
び帯電減衰速度に応じて調整される。In the present invention, the coating agent for coating the core material is
It is necessary to contain a copolymer of vinylidene fluoride and trifluoroethylene or hexafluoropropylene as an essential component. Even if the coating material is composed only of a copolymer of vinylidene fluoride and trifluoroethylene or hexafluoropropylene, it will have sufficient chargeability and film-forming properties for practical use, but the charge cannot be adjusted freely. In order to improve the strength and adhesion between the coating material and the core, it is preferable to use an acrylic acid ester polymer or copolymer, or a trifluoromonochloroethylene-vinyl chloride copolymer. The mixing ratio of the copolymer of vinylidene fluoride and trifluoroethylene or hexafluoropropylene and the acrylic acid ester polymer or trifluoromonochloroethylene-vinyl chloride copolymer is usually 99; 1 to 20 by weight.
:80 is appropriate, and is adjusted according to the charge increase rate and charge decay rate of the toner used.
本発明において用いられるフッ化ビニリデンとトリフロ
ロエチレン又はヘキサフロロプロピレンとの共重合体は
、乳化重合又は懸濁重合によって製造される。フッ化ビ
ニリデンとトリフロロエチレン又はヘキサフロロプロピ
レンとの共重合比は、90:10〜50:50の範囲が
適当である。また、溶液粘度が0.7〜1.5、融点(
1曹p)が130〜160’Cの範囲にあるものが好ま
しい。The copolymer of vinylidene fluoride and trifluoroethylene or hexafluoropropylene used in the present invention is produced by emulsion polymerization or suspension polymerization. The copolymerization ratio of vinylidene fluoride and trifluoroethylene or hexafluoropropylene is suitably in the range of 90:10 to 50:50. In addition, the solution viscosity is 0.7 to 1.5, the melting point (
It is preferable that the monocarbonate p) is in the range of 130 to 160'C.
一方、上記共重合体と共に使用することができるアクリ
ル酸エステル重合体又は共重合体の構成成分であるアク
リル酸エステルは、アクリル酸又はメタクリル酸と各種
アルコールとのエステル類があげられる。その様なアル
コールとしては、例えば、メチルアルコール、エチルア
ルコール、プロピルアルコール、ブチルアルコール、ア
ミルアルコール、ヘキシルアルコール、ヘプチルアルコ
ール、オクチルアルコール、ノニルアルコール、ドデシ
ルアルコール、テトラデシルアルコール、ヘキサデシル
アルコールの如きアルカノール;これ等アルカノールの
一部をハロゲン化したハロゲン化アルカノール;メトキ
シエチルアルコール、エトキシエチルアルコール、メト
キシプロピルアルコール、エトキシプロピルアルコール
の如きアルコキシアルカノール;ベンジルアルコール、
フェネチルアルコール、フェニルプロピルアルコールの
如きアラルキルアルコール;アリルアルコール、タロト
ニルアルコールの如きアルケニルアルコール等があげら
れる。On the other hand, examples of the acrylic ester polymer or acrylic ester that is a constituent component of the copolymer that can be used with the above copolymer include esters of acrylic acid or methacrylic acid and various alcohols. Such alcohols include, for example, alkanols such as methyl alcohol, ethyl alcohol, propyl alcohol, butyl alcohol, amyl alcohol, hexyl alcohol, heptyl alcohol, octyl alcohol, nonyl alcohol, dodecyl alcohol, tetradecyl alcohol, and hexadecyl alcohol; Halogenated alkanols in which a part of these alkanols is halogenated; alkoxyalkanols such as methoxyethyl alcohol, ethoxyethyl alcohol, methoxypropyl alcohol, and ethoxypropyl alcohol; benzyl alcohol,
Examples include aralkyl alcohols such as phenethyl alcohol and phenylpropyl alcohol; alkenyl alcohols such as allyl alcohol and tarotonyl alcohol.
また、上記アクリル酸エステルは、1種又は2種以上共
重合させてもよいが、必要に応じて、他の共重合可能な
モノマーの1種又は2種以上と共重合させてもよい。そ
の場合アクリル酸エステル類が、全モノマーの25重量
%以上、好ましくは50重量%以上占めることが好まし
い。Further, the above acrylic acid ester may be copolymerized alone or with two or more types, and may be copolymerized with one or more types of other copolymerizable monomers, if necessary. In that case, it is preferred that the acrylic esters account for 25% by weight or more, preferably 50% by weight or more of the total monomers.
本発明において使用するコア物質としては、鉄粉末、酸
化鉄粉末、カルボニル鉄粉末、マグネタイト、ニッケル
及びフェライト等の粉末を例示することができ、通常キ
ャリアとして10〜500μmの粒径となるような大き
さのものが使用される。Examples of the core material used in the present invention include powders such as iron powder, iron oxide powder, carbonyl iron powder, magnetite, nickel, and ferrite, and usually as a carrier, particles of a size of 10 to 500 μm are used. The one that is the same is used.
本発明におけるキャリア粒子は、前記のようなコア物質
に、前記の被覆剤を用いて表面処理し、コア物質表面上
に、化学結合或いは吸着によって被覆層を形成すること
により得ることができる。The carrier particles in the present invention can be obtained by surface-treating the core material as described above using the coating agent as described above, and forming a coating layer on the surface of the core material by chemical bonding or adsorption.
コア物質の表面処理のためには、例えば前記の重合体の
1種又は2種以上の混合物を適当な溶媒に溶解して得ら
れる溶液中にコア物質を浸漬し、その後に脱溶媒、乾燥
、高温焼き付けをする方法等を利用することができる。For surface treatment of the core material, for example, the core material is immersed in a solution obtained by dissolving one or more of the above-mentioned polymers in a suitable solvent, followed by desolvation, drying, A method such as baking at a high temperature can be used.
これ等の方法において、高温焼き付は処理は必ずしも必
要ではない。In these methods, high temperature baking treatment is not necessarily required.
前記重合体の被覆量は、通常コア物質に対して0.05
〜3.0重量%であることが好ましい。The coating amount of the polymer is usually 0.05% of the core material.
It is preferably 3.0% by weight.
一方、上記の負帯電キャリアと混合される正帯電トナー
は、結着樹脂中に磁性体微粒子を含有するものであるが
、磁性体微粒子としては、四三酸化鉄、HnZnフェラ
イト、Mienフェライト等、通常用いられる磁性粉な
らば、如何なるものでも使用可能である。これ等磁性体
微粒子は、通常トナー中に5〜20重量%含有させるこ
とが好ましい。On the other hand, the positively charged toner mixed with the above negatively charged carrier contains magnetic fine particles in the binder resin, and the magnetic fine particles include triiron tetroxide, HnZn ferrite, Mien ferrite, etc. Any commonly used magnetic powder can be used. It is usually preferable that the toner contains 5 to 20% by weight of these magnetic particles.
また、結着樹脂としては、スチレン樹脂、スチレン−ア
クリル共重合体、ポリオレフィン、ポリエステル樹脂、
エポキシ樹脂、その他、通常トナーに使用される材料な
らば、如何なるものでも使用可能である。In addition, as the binder resin, styrene resin, styrene-acrylic copolymer, polyolefin, polyester resin,
Epoxy resin and any other materials commonly used in toners can be used.
本発明における正帯電トナーには、着色剤として、各種
の染料、顔料、例えはカーボンブラック等を含有させる
ことができる。The positively charged toner of the present invention can contain various dyes and pigments, such as carbon black, as colorants.
本発明において、上記トナーの粒子表面には、二酸化ケ
イ素、酸化アルミニウム、酸化チタン、ステアリン酸亜
鉛、樹脂微粉末等のトナーの平均粒径よりも小さい微細
粒子を外添によって付着させることができる。In the present invention, fine particles smaller than the average particle size of the toner, such as silicon dioxide, aluminum oxide, titanium oxide, zinc stearate, and fine resin powder, can be attached to the surface of the toner particles by external addition.
本発明の磁気ブラシ現像用二成分現像剤は、上記の負帯
電キャリアと正−!4F電トナーとを混合することによ
って得られる。The two-component developer for magnetic brush development of the present invention comprises the above-mentioned negatively charged carrier and positively charged carrier. It is obtained by mixing with 4F electric toner.
実施例 以下、本発明を実施例によって更に具体的に説明する。Example Hereinafter, the present invention will be explained in more detail with reference to Examples.
しかしながら、本発明は、これ等の実施例によって同等
限定されるものではない。However, the present invention is not equally limited by these examples.
実施例1
フッ化ビニリデンとトリフロロエチレンの共重合体(共
重合比85:15 ) 16重量部、及びポリメチルメ
タクリレート4重量部をジメチルホルムアミド100重
量部に溶解し、得られた溶液を平均粒径100圃の球状
酸化鉄粉2000重量部に加え、減圧型ニーダ−コータ
を用いて被覆処理を行い、負帯電キャリアを得た。Example 1 16 parts by weight of a copolymer of vinylidene fluoride and trifluoroethylene (copolymerization ratio 85:15) and 4 parts by weight of polymethyl methacrylate were dissolved in 100 parts by weight of dimethylformamide, and the resulting solution was dissolved into average particles. In addition to 2000 parts by weight of spherical iron oxide powder having a diameter of 100 fields, a coating treatment was performed using a vacuum kneader coater to obtain a negatively charged carrier.
一方、スチレン80重量部%及びブチルアクリレート2
0重量%からなる共重合体75重量部(分子量的200
,000 ) 、カーボンブラック10重量部、磁性体
微粒子(マグネタイト)12重量部、及び帯電調節剤3
重量部を、加圧ニーダ−によって混練し、冷却した後、
ハンマーミル、次いで、ジェットミルで粉砕し、更に分
級して、平均粒径10aのトナーを得た。On the other hand, 80 parts by weight of styrene and 2 parts by weight of butyl acrylate
75 parts by weight of copolymer consisting of 0% by weight (molecular weight 200%
,000), 10 parts by weight of carbon black, 12 parts by weight of magnetic fine particles (magnetite), and 3 parts by weight of charge control agent.
After kneading the parts by weight using a pressure kneader and cooling,
The powder was pulverized using a hammer mill, then a jet mill, and further classified to obtain a toner having an average particle size of 10a.
得られたトナー3重量部を、前記キャリア100重量部
と混合して、磁気ブラシ現像用二成分現像剤を得た。Three parts by weight of the obtained toner were mixed with 100 parts by weight of the carrier to obtain a two-component developer for magnetic brush development.
実施例2
フッ化ビニリデンとへキサフロロプロピレンの共重合体
(共重合比80:20 ) 20重量部をジメチルホル
ムアミド100重量部に溶解し、得られた溶液を平均粒
径100ρの球状酸化鉄粉2000重量部に加え、減圧
型ニーダ−コータを用いて被覆処理を行い、負帯電キャ
リアを得た。Example 2 20 parts by weight of a copolymer of vinylidene fluoride and hexafluoropropylene (copolymerization ratio 80:20) was dissolved in 100 parts by weight of dimethylformamide, and the resulting solution was mixed into spherical iron oxide powder with an average particle size of 100ρ. In addition to 2000 parts by weight, coating was performed using a vacuum kneader coater to obtain a negatively charged carrier.
次に、実施例1と同様に操作して磁気ブラシ現像用二成
分現像剤を得た。Next, the same procedure as in Example 1 was carried out to obtain a two-component developer for magnetic brush development.
比較例1
実施例1において、フッ化ビニリデンとトリフロロエチ
レンの共重合体を、フッ化ビニリデン単独重合体に変更
する以外は、実施例1におけると同様に操作して磁気ブ
ラシ現像用二成分現像剤を得た。Comparative Example 1 Two-component development for magnetic brush development was carried out in the same manner as in Example 1, except that the copolymer of vinylidene fluoride and trifluoroethylene in Example 1 was changed to vinylidene fluoride homopolymer. obtained the drug.
比較例2
実施例1において、トナー中の磁性体微粒子をスチレン
−ブチルアクリレート共重合体に置換した以外は、実施
例1におけると同様に操作して磁気ブラシ現像用二成分
現像剤を得た。Comparative Example 2 A two-component developer for magnetic brush development was obtained in the same manner as in Example 1, except that the magnetic fine particles in the toner were replaced with styrene-butyl acrylate copolymer.
上記実施例1及び2、比較例1及び2における磁気ブラ
シ現像用二成分現像剤を用い、電子写真複写機(ゼロッ
クス1065 (有機光導電性ベルト型感光体を使用)
、七ロックス株製)によって、連続複写試験を行った。Using the two-component developer for magnetic brush development in Examples 1 and 2 and Comparative Examples 1 and 2 above, an electrophotographic copying machine (Xerox 1065 (using an organic photoconductive belt type photoreceptor))
A continuous copying test was carried out using the following method.
結果は、下記表に示すごとくであった。The results were as shown in the table below.
注)■帯電量は、ブローオフ測定器により測定。Note) ■The amount of charge is measured using a blow-off measuring device.
■被覆剤の剥離は、走査型電子顕微鏡により観察。■ Peeling of the coating was observed using a scanning electron microscope.
■寿命は、原稿濃度1.0部分が0.7以下で、白地部
分が0.03以上の時をもって、その寿命と判定。■The lifespan is determined when the original density 1.0 part is 0.7 or less and the white part is 0.03 or more.
発明の効果
本発明の磁気ブラシ現像用二成分現像剤は、上記の構成
を有するから、帯電上昇速度が高く、耐表面汚染性が良
好なため、ランニング時における帯電量の低下を起すこ
とがない、したがって、カブリの早期発生や機内汚染を
生じることがない。Effects of the Invention Since the two-component developer for magnetic brush development of the present invention has the above-mentioned structure, it has a high charging rate and good surface stain resistance, so it does not cause a decrease in the amount of charging during running. Therefore, there is no possibility of early fogging or internal contamination.
また、磁性トナーを上記キャリアと組み合わせて使用す
るため、トナーによる機内汚染を生じることがなく、寿
命も長いので、長期間安定して良質な画質のコピー画像
を得ることかできる。Furthermore, since the magnetic toner is used in combination with the above-mentioned carrier, there is no contamination of the inside of the machine due to the toner, and the service life is long, so that copy images of good quality can be obtained stably for a long period of time.
特許出願人 富士ゼロックス株式会社代理人
弁理士 渡部 剛Patent applicant Fuji Xerox Co., Ltd. Agent
Patent Attorney Tsuyoshi Watanabe
Claims (1)
サフロロプロピレンとの共重合体を必須成分として含有
する被覆剤で被覆された負帯電キャリアと、磁性体微粒
子を含有する正帯電トナーとからなることを特徴とする
磁気ブラシ現像用二成分現像剤。(1) Consisting of a negatively charged carrier coated with a coating agent containing a copolymer of vinylidene fluoride and trifluoroethylene or hexafluoropropylene as an essential component, and a positively charged toner containing magnetic fine particles. A two-component developer for magnetic brush development.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63238872A JPH0287158A (en) | 1988-09-26 | 1988-09-26 | Binary developer |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63238872A JPH0287158A (en) | 1988-09-26 | 1988-09-26 | Binary developer |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0287158A true JPH0287158A (en) | 1990-03-28 |
Family
ID=17036515
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63238872A Pending JPH0287158A (en) | 1988-09-26 | 1988-09-26 | Binary developer |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0287158A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6653037B2 (en) | 2000-11-20 | 2003-11-25 | Ricoh Company, Ltd. | Toner for developing latent electrostatic images, and image forming method and device |
-
1988
- 1988-09-26 JP JP63238872A patent/JPH0287158A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6653037B2 (en) | 2000-11-20 | 2003-11-25 | Ricoh Company, Ltd. | Toner for developing latent electrostatic images, and image forming method and device |
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