JPH0833684B2 - Carrier for developer - Google Patents
Carrier for developerInfo
- Publication number
- JPH0833684B2 JPH0833684B2 JP62014078A JP1407887A JPH0833684B2 JP H0833684 B2 JPH0833684 B2 JP H0833684B2 JP 62014078 A JP62014078 A JP 62014078A JP 1407887 A JP1407887 A JP 1407887A JP H0833684 B2 JPH0833684 B2 JP H0833684B2
- Authority
- JP
- Japan
- Prior art keywords
- carrier
- functional group
- magnetic
- vinyl
- developer
- 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 - Lifetime
Links
- 125000000524 functional group Chemical group 0.000 claims description 19
- 239000002245 particle Substances 0.000 claims description 18
- 229920005989 resin Polymers 0.000 claims description 14
- 239000011347 resin Substances 0.000 claims description 14
- 229920000098 polyolefin Polymers 0.000 claims description 12
- 239000011230 binding agent Substances 0.000 claims description 11
- 238000001816 cooling Methods 0.000 claims description 7
- 239000006247 magnetic powder Substances 0.000 claims description 3
- 239000012876 carrier material Substances 0.000 claims description 2
- 239000000155 melt Substances 0.000 claims 1
- 230000005291 magnetic effect Effects 0.000 description 17
- -1 olefin compound Chemical class 0.000 description 10
- 239000010419 fine particle Substances 0.000 description 8
- 239000000969 carrier Substances 0.000 description 7
- 238000000034 method Methods 0.000 description 6
- 239000004698 Polyethylene Substances 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 5
- 229920000573 polyethylene Polymers 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 238000005507 spraying Methods 0.000 description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 239000006249 magnetic particle Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000001993 wax Substances 0.000 description 4
- 235000010724 Wisteria floribunda Nutrition 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000007334 copolymerization reaction Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 125000002843 carboxylic acid group Chemical group 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 239000007822 coupling agent Substances 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- YBQJKVOFUMFBDE-UHFFFAOYSA-N methyl 2-methylprop-2-enoate;prop-2-enoic acid;styrene Chemical compound OC(=O)C=C.COC(=O)C(C)=C.C=CC1=CC=CC=C1 YBQJKVOFUMFBDE-UHFFFAOYSA-N 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 108091008695 photoreceptors Proteins 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- UZKWTJUDCOPSNM-UHFFFAOYSA-N 1-ethenoxybutane Chemical compound CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- SBYMUDUGTIKLCR-UHFFFAOYSA-N 2-chloroethenylbenzene Chemical compound ClC=CC1=CC=CC=C1 SBYMUDUGTIKLCR-UHFFFAOYSA-N 0.000 description 1
- XVTXLKJBAYGTJS-UHFFFAOYSA-N 2-methylpenta-1,4-dien-3-one Chemical compound CC(=C)C(=O)C=C XVTXLKJBAYGTJS-UHFFFAOYSA-N 0.000 description 1
- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 229910001111 Fine metal Inorganic materials 0.000 description 1
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229920000800 acrylic rubber Polymers 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- XZKRXPZXQLARHH-UHFFFAOYSA-N buta-1,3-dienylbenzene Chemical compound C=CC=CC1=CC=CC=C1 XZKRXPZXQLARHH-UHFFFAOYSA-N 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- MEGHWIAOTJPCHQ-UHFFFAOYSA-N ethenyl butanoate Chemical compound CCCC(=O)OC=C MEGHWIAOTJPCHQ-UHFFFAOYSA-N 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000003302 ferromagnetic material Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 230000026030 halogenation Effects 0.000 description 1
- 238000005658 halogenation reaction Methods 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- PBZROIMXDZTJDF-UHFFFAOYSA-N hepta-1,6-dien-4-one Chemical compound C=CCC(=O)CC=C PBZROIMXDZTJDF-UHFFFAOYSA-N 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 1
- 239000002346 layers by function Substances 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- HILCQVNWWOARMT-UHFFFAOYSA-N non-1-en-3-one Chemical compound CCCCCCC(=O)C=C HILCQVNWWOARMT-UHFFFAOYSA-N 0.000 description 1
- 229940065472 octyl acrylate Drugs 0.000 description 1
- ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- UCUUFSAXZMGPGH-UHFFFAOYSA-N penta-1,4-dien-3-one Chemical class C=CC(=O)C=C UCUUFSAXZMGPGH-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 125000005010 perfluoroalkyl group Chemical group 0.000 description 1
- WRAQQYDMVSCOTE-UHFFFAOYSA-N phenyl prop-2-enoate Chemical compound C=CC(=O)OC1=CC=CC=C1 WRAQQYDMVSCOTE-UHFFFAOYSA-N 0.000 description 1
- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 229920005792 styrene-acrylic resin Polymers 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- FUSUHKVFWTUUBE-UHFFFAOYSA-N vinyl methyl ketone Natural products CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 1
- 229910000859 α-Fe Inorganic materials 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
- G03G9/10—Developers with toner particles characterised by carrier particles
- G03G9/107—Developers with toner particles characterised by carrier particles having magnetic components
- G03G9/1088—Binder-type carrier
- G03G9/10882—Binder is obtained by reactions only involving carbon-carbon unsaturated bonds
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Developing Agents For Electrophotography (AREA)
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、静電印刷法等に
おいて、静電潜像または磁気潜像を現像する2成分現像
剤の構成成分であるキャリヤ、更に詳しく言えば磁性体
分散型キャリヤに関する。The present invention relates to a two-component developer for developing an electrostatic latent image or a magnetic latent image in electrophotography, electrostatic recording, electrostatic printing, and the like. The present invention relates to a carrier which is a constituent component, and more particularly, to a carrier in which a magnetic substance is dispersed.
[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、種々の手段により電気的潜
像を形成し、この潜像に磁気ブラシ現像法等を用いてト
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。[Prior Art] In electrophotography, a photoconductive substance such as selenium is used as a photoreceptor, an electric latent image is formed by various means, and the latent image is formed by a magnetic brush developing method or the like. A method of visualizing an image by attaching toner is generally adopted.
この現像工程において、トナーに適当量の正または負
の電気量を付与するためにキャリヤと呼ばれる担体粒子
が使用される。キャリヤとしては種々のタイプのものが
開発され、実用化されている。In this developing process, carrier particles called carriers are used to give an appropriate amount of positive or negative electric charge to the toner. Various types of carriers have been developed and put into practical use.
[発明が解決しようとする問題点] キャリヤ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、
現像性、現像剤寿命等を挙げることができる。[Problems to be Solved by the Invention] Although there are various characteristics required for the carrier, appropriate charging characteristics, impact resistance, abrasion resistance,
Developability, developer life, etc. can be mentioned.
上記諸要求特性を考慮すると、従来使用されてきたキ
ャリヤは依然として改善すべき問題を残しており、充分
に満足できるものは知られていない。例えば、酸化鉄粉
をはじめとする導電性キャリヤはソリッド現像性には優
れているものの細線再現性に劣り、また寿命延長のため
に特殊な帯電制御剤をトナーに含有せしめることを必要
とする等の欠点を有し、一方コート系の絶縁性キャリヤ
は寿命、細線の再現性等には優れているものの、ソリッ
ド再現性に劣るという欠点を有している。これらの欠点
を改良する目的で磁性微粒子を結着樹脂中に分散せしめ
た小粒径キャリヤ、いわゆるマイクロトーニング用キャ
リヤが提案され、実用化されているが、小粒径に起因し
てキャリヤが感光体へ付着するという不都合を有する。
この現象はキャリヤを大粒径化することによって防止す
ることが可能であるが、キャリヤの大粒径化により帯電
性が低下し、その結果、カブリの発生や機内汚染等の問
題が生じる。In view of the above-mentioned required characteristics, conventionally used carriers still have problems to be improved, and no satisfactory carrier has been known. For example, conductive carriers such as iron oxide powder are excellent in solid developability, but inferior in fine line reproducibility, and require a special charge control agent to be included in the toner to extend the life. On the other hand, the coated insulating carrier is excellent in life, reproducibility of fine wires, etc., but is inferior in solid reproducibility. For the purpose of remedying these drawbacks, small particle size carriers in which magnetic fine particles are dispersed in a binder resin, so-called microtoning carriers, have been proposed and put into practical use. It has the disadvantage of adhering to the body.
This phenomenon can be prevented by increasing the particle size of the carrier. However, the increase in the particle size of the carrier lowers the chargeability. As a result, problems such as generation of fog and contamination in the machine occur.
従って、本発明の主な目的は電子写真法、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磁気
ブラシ現像用キャリヤを提供することにある。Accordingly, a main object of the present invention is to provide a novel magnetic brush developing carrier used for developing an electrostatic latent image in electrophotography and electrostatic recording.
本発明の他の目的は、帯電量の低下を防止し、その結
果カブリの早期発生、機内汚染が生ずることがなく、更
に現像剤寿命、高速現像性に優れた磁気ブラシ現像用キ
ャリヤを提供することにある。Another object of the present invention is to provide a carrier for magnetic brush development, which prevents a decrease in charge amount, as a result, does not cause fog early generation and in-machine contamination, and has excellent developer life and high-speed developability. Especially.
[問題点を解決するための手段] 本発明は、前記及びその他の目的を、官能基を有する
ポリオレフィンを含有する結着樹脂と磁性粉を必須成分
とするキャリア材料溶融物を噴霧冷却することにより得
られる平均粒径が20〜400μmであることを特徴とする
現像剤用キャリアにより達成したものである。[Means for Solving the Problems] The present invention has the above and other objects by spray cooling a binder resin containing a polyolefin having a functional group and a carrier material melt containing magnetic powder as essential components. This is achieved by a carrier for a developer, which is characterized in that the obtained average particle size is 20 to 400 μm.
本発明においてポリオレフィンに導入される官能基と
しては、例えば水酸基、カルボン酸基、エステル基、カ
ルボニル基、エーテル基等の含酸素官能基、アミノ、ア
ミド、イミド、ニトリル等の含窒素官能基、塩素、フッ
素、パーフロロアルキル基等の含ハロゲン官能基、フェ
ニル、ナフチル等の芳香族基、ケイ素原子含有基等が挙
げられ、これらのうち好ましいのは、カルボン酸基、水
酸基、アミノ基、フェニル基である。これらの官能基は
単独あるいは二種以上の組合わせで用いることができ
る。The functional group introduced into the polyolefin in the present invention, for example, a hydroxyl group, a carboxylic acid group, an ester group, a carbonyl group, an oxygen-containing functional group such as an ether group, a nitrogen-containing functional group such as amino, amide, imide, nitrile, chlorine , Fluorine, halogen-containing functional groups such as perfluoroalkyl groups, aromatic groups such as phenyl and naphthyl, silicon atom-containing groups, and the like. Of these, preferred are carboxylic acid groups, hydroxyl groups, amino groups, and phenyl groups. Is. These functional groups can be used alone or in combination of two or more.
ポリオレフィンの官能基の導入法は官能基にあわせて
種々の方法が取られるが、酸化、還元、ハロゲン化等の
ポリオレフィンに対する直接化学処理、オレフィンモノ
マーと官能基含有モノマーとの共重合、ポリオレフィン
と官能基含有モノマーとの共存重合、官能基含有ポリマ
ーとオレフィンモノマーの共存重合等の方法が例示でき
る。Various methods can be used to introduce a functional group of a polyolefin, depending on the functional group, such as direct chemical treatment of the polyolefin such as oxidation, reduction and halogenation, copolymerization of an olefin monomer and a functional group-containing monomer, polyolefin and a functional group. Examples of the method include co-polymerization with a group-containing monomer and co-polymerization with a functional group-containing polymer and an olefin monomer.
本発明で用いられるオレフィン系化合物としては、エ
チレン、プロピレン、ブチレン、イソブチレン等が例示
できる。Examples of the olefin compound used in the present invention include ethylene, propylene, butylene, isobutylene and the like.
本発明において用いられるキャリヤの結着樹脂として
は、一般の熱可塑性樹脂群の全てを用いることができる
が、具体的には、スチレン、クロルスチレン、ビニルス
チレン等のスチレン類:エチレン、プロピレン、ブチレ
ン、イソブチレン等のモノオレフィン:酢酸ビニル、プ
ロピオン酸ビニル、安息香酸ビニル、酪酸ビニル等のビ
ニルエステル:アクリル酸メチル、アクリル酸エチル、
アクリル酸ブチル、アクリル酸ドデシル、アクリル酸オ
クチル、アクリル酸フェニル、メタクリル酸メチル、メ
タクリル酸エチル、メタクリル酸ブチル、メタクリル酸
ドデシル等のα−メチレン脂肪族モノカルボン酸のエス
テル:ビニルメチルエーテル、ビニルエチルエーテル、
ビニルブチルエーテル等のビニルエーテル:ビニルメチ
ルケトン、ビニルヘキシルケトン、ビニルイソプロペニ
ルケトン等のビニルケトン類の単独重合体あるいは共重
合体を例示することができ、特に代表的な結着樹脂とし
ては、ポリスチレン、スチレン−アクリル酸アルキル共
重合体、スチレン−メタクリル酸アルキル共重合体、ス
チレン−アクリロニトリル共重合体、スチレン−ブタジ
エン共重合体、スチレン−無水マレイン酸共重合体、ポ
リエチレン、ポリプロピレンを挙げることができる。As the binder resin for the carrier used in the present invention, all of the general thermoplastic resin group can be used, but specifically, styrenes such as styrene, chlorostyrene, vinyl styrene: ethylene, propylene, butylene. , Monobutyl olefin such as isobutylene: vinyl acetate, vinyl propionate, vinyl benzoate, vinyl ester such as vinyl butyrate: methyl acrylate, ethyl acrylate,
Ester of α-methylene aliphatic monocarboxylic acid such as butyl acrylate, dodecyl acrylate, octyl acrylate, phenyl acrylate, methyl methacrylate, ethyl methacrylate, butyl methacrylate, dodecyl methacrylate: vinyl methyl ether, vinyl ethyl ether,
Vinyl ethers such as vinyl butyl ether: homopolymers or copolymers of vinyl ketones such as vinyl methyl ketone, vinyl hexyl ketone, vinyl isopropenyl ketone and the like can be exemplified, and particularly typical binder resins are polystyrene and styrene. Examples thereof include an alkyl acrylate copolymer, a styrene-alkyl methacrylate copolymer, a styrene-acrylonitrile copolymer, a styrene-butadiene copolymer, a styrene-maleic anhydride copolymer, polyethylene and polypropylene.
更に、ポリエステル、ポリウレタン、エポキシ樹脂、
シリコン樹脂、ポリアミド、変性ロジン、パラフィン、
ワックス類を挙げることができる。Furthermore, polyester, polyurethane, epoxy resin,
Silicone resin, polyamide, modified rosin, paraffin,
Waxes can be mentioned.
本発明において、結着樹脂中に含有させる官能基を有
するポリオレフィンの量はキャリヤ成分の総量に対して
1〜70重量%である。In the present invention, the amount of the functional group-containing polyolefin contained in the binder resin is 1 to 70% by weight based on the total amount of carrier components.
本発明において使用する磁性微粒子は通常用いられる
強磁性体の微粒子を全て用いることができるが、具体的
には四三酸化鉄、γ−三二酸化鉄、各種フェライト粉、
酸化クロム、各種金属微粉等が挙げられる。The magnetic fine particles used in the present invention may be all fine particles of a ferromagnetic material that are usually used, but specifically, ferric tetroxide, γ-iron sesquioxide, various ferrite powders,
Examples include chromium oxide and various fine metal powders.
磁性粒子の含有量は結着樹脂全量に対し通常30〜95重
量%程度であり、望ましくは45〜90重量%の配合が良好
な結果を与える。The content of the magnetic particles is usually about 30 to 95% by weight, preferably 45 to 90% by weight, based on the total amount of the binder resin, to give good results.
次にキャリヤ製造方法は前記結着樹脂、官能基含有ポ
リオレフィン及び磁性微粒子を必須成分とし、これらと
他の成分を加熱溶融混合し、その混合物を固化させない
状態で比較的低温の空気流により冷却固化することによ
って製造される。Next, in the carrier production method, the binder resin, the functional group-containing polyolefin and the magnetic fine particles are essential components, and these components and other components are heated and melt mixed, and the mixture is solidified by cooling with an air stream at a relatively low temperature without solidifying the mixture. Is manufactured by
さらに詳述すれば、その製造装置は前処理設備として
加熱溶融混合装置及び混練物粘度調整槽を備え、さらに
噴霧装置まで混練物を搬送するポンプ及び噴霧した混練
物を冷却固化させる冷却塔で構成されているものが使用
される。More specifically, the manufacturing apparatus includes a heating and melting mixer as a pretreatment facility and a kneaded material viscosity adjusting tank, and further includes a pump for conveying the kneaded material to a spraying device and a cooling tower for cooling and solidifying the sprayed kneaded material. What is used is used.
加熱溶融混合装置としては、ニーダー、ロールミル、
バンバリー、サンドミル、アトライター、ヘンシェルミ
キサー等の使用が可能であり、噴霧装置としては、ノズ
ル式又は円板式のものが小粒径のキャリヤを得るのに比
較的適しているが、これらに限定されるものではない。As a heating and melting and mixing device, a kneader, a roll mill,
It is possible to use a Banbury, a sand mill, an attritor, a Henschel mixer, etc., and as a spraying device, a nozzle type or a disc type is relatively suitable for obtaining a carrier having a small particle size, but is not limited to these. Not something.
結着樹脂、官能基含有ポリオレフィン及び磁性微粒子
の他に帯電制御、分散向上、強度補強、流動性向上その
他の目的で樹脂、帯電制御剤、カップリング剤、フィラ
ー、その他の微粉末等をキャリヤ内部に添加することも
できる。In addition to binder resin, functional group-containing polyolefin and magnetic fine particles, resin, charge control agent, coupling agent, filler, other fine powder, etc. inside the carrier for charge control, dispersion improvement, strength reinforcement, fluidity improvement and other purposes. Can also be added to.
本発明のキャリヤ粒子はそのままキャリヤ粒子として
用いることもできるが、高い表面平滑性を有し、かつ球
形であるため表面を樹脂、カップリング剤、界面活性
剤、帯電制御剤、微粉末等により表面処理、被覆処理を
施すことができる。The carrier particles of the present invention can be used as they are as carrier particles, but since they have high surface smoothness and are spherical, the surface is treated with a resin, coupling agent, surfactant, charge control agent, fine powder or the like. Treatment or coating treatment can be applied.
本発明のキャリヤ粒子は前述の現像剤寿命と感光体キ
ャリヤ付着及び画質とのバランス上から平均粒径20〜40
0μm、より望ましくは30〜200μmとするのが適当であ
る。The carrier particles of the present invention have an average particle size of 20 to 40 in view of the balance between the developer life and the adhesion of the photoreceptor carrier and the image quality.
It is suitable that the thickness is 0 μm, more preferably 30 to 200 μm.
かくして得られる本発明のキャリヤはトナーと混合し
て静電潜像現像用の磁性ブラシ現像剤として使用され
る。The carrier of the present invention thus obtained is mixed with a toner and used as a magnetic brush developer for developing an electrostatic latent image.
トナーとしては結着樹脂中に着色剤を分散させた、通
常の電子写真法で使用されているいかなる帯電性トナー
を使用することもでき、特に制限されない。As the toner, any chargeable toner in which a colorant is dispersed in a binder resin and which is used in a usual electrophotographic method can be used and is not particularly limited.
[発明の効果] 本発明の磁気ブラシ現像用キャリヤは、官能基を有す
るポリオレフィンを含有する結着樹脂と磁性粉を必須成
分とするキャリヤ材料溶融物を噴霧冷却することにより
得られるものであり、以下に示す効果が達成される。[Advantages of the Invention] The magnetic brush developing carrier of the present invention is obtained by spray cooling a carrier resin melt containing a binder resin containing a polyolefin having a functional group and magnetic powder as essential components. The following effects are achieved.
まず、ポリオレフィン中の官能基の種類、量を調整す
ることにより、キャリヤの帯電性を自由に制御すること
ができる。First, the chargeability of the carrier can be freely controlled by adjusting the type and amount of the functional group in the polyolefin.
またフッ素系官能基、シリコン系官能基等低表面エネ
ルギー性の基を導入するとキャリヤの表面エネルギーが
低下し、キャリヤへのトナーインパクションが減少し長
寿命化が可能となる。Further, when a low surface energy group such as a fluorine-based functional group or a silicon-based functional group is introduced, the surface energy of the carrier is lowered, the toner impaction on the carrier is reduced, and the life can be extended.
さらに、キャリヤ粒子に被覆処理を施す場合、被覆材
料と親和性の良い官能基をポリオレフィンに導入するこ
とによって、被覆層の剥離を防止することが可能とな
る。Furthermore, when the carrier particles are subjected to the coating treatment, the functional layer having a good affinity for the coating material is introduced into the polyolefin, whereby the peeling of the coating layer can be prevented.
[実施例] 以下、実施例および比較例により本発明を更に具体的
に説明する。しかしながら、本発明はこれらの例により
何等限定されるものではない。なお、下記の例中、部は
重量部を表わす。[Examples] Hereinafter, the present invention will be described more specifically with reference to Examples and Comparative Examples. However, the invention is not limited in any way by these examples. In the following examples, parts represent parts by weight.
実施例1 磁性微粒子(EPT−1000,戸田工業社製) 80部 ポリエチレン(三井ハイワックス400P,三井石油化学社
製) 10部 カルボキシル基を導入したポリエチレン(酸価:20KOH m
g) 10部 を加圧ニーダーで加熱溶融混練した。Example 1 Magnetic fine particles (EPT-1000, manufactured by Toda Kogyo Co., Ltd.) 80 parts Polyethylene (Mitsui High Wax 400P, manufactured by Mitsui Petrochemical Co., Ltd.) 10 parts Polyethylene introduced with a carboxyl group (acid value: 20 KOH m
g) 10 parts were heat-melted and kneaded with a pressure kneader.
次いで、円板式の噴霧装置を用いて噴霧冷却して固化
した後分級し、平均粒径100μmの本発明に係る球形磁
性粒子分散型キャリヤを得た。Then, the mixture was spray-cooled using a disk-type spraying device to solidify and then classified to obtain a spherical magnetic particle-dispersed carrier according to the present invention having an average particle diameter of 100 μm.
比較例1 磁性微粒子(EPT1000,戸田工業社製) 80部 ポリエチレン(三井ハイワックス400P,三井石油化学社
製) 20部 を実施例1と同様の方法で、混練、造粒、分級し、平均
粒径100μmの球形磁性粒子分散型キャリヤを得た。Comparative Example 1 Magnetic fine particles (EPT1000, manufactured by Toda Kogyo Co., Ltd.) 80 parts Polyethylene (Mitsui High Wax 400P, manufactured by Mitsui Petrochemical Co., Ltd.) 20 parts were kneaded, granulated, classified and averaged in the same manner as in Example 1. A spherical magnetic particle dispersion type carrier having a diameter of 100 μm was obtained.
実施例2 磁性微粒子(EPT1000,戸田工業社製) 80部 ポリエチレン(三井ハイワックス400P,三井石油化学社
製) 15部 ポリエチレン−スチレン(8:2)共重合体 5部 を加圧ニーダーで加熱溶融混練した。Example 2 Magnetic fine particles (EPT1000, manufactured by Toda Kogyo Co., Ltd.) 80 parts Polyethylene (Mitsui High Wax 400P, manufactured by Mitsui Petrochemical Co., Ltd.) 15 parts Polyethylene-styrene (8: 2) copolymer 5 parts Heat melting with a pressure kneader Kneaded
その後、円板式の噴霧装置を用いて噴霧、冷却、固化
した後、分級し、平均粒径100μmの本発明に係る球形
磁性粒子分散型キャリヤを得た。Then, after spraying, cooling and solidifying using a disk type spraying device, classification was carried out to obtain a spherical magnetic particle dispersed carrier according to the present invention having an average particle size of 100 μm.
実施例3 実施例2で得られたキャリヤ粒子100部に対し、スチ
レン−メタクリル酸メチル−アクリル酸(80:15:5)共
重合体0.5部の10%アセトン溶液を流動層コーティング
装置を用いてコートし本発明に係るコート型球形磁性粒
子分散型キャリヤを得た。Example 3 To 100 parts of the carrier particles obtained in Example 2, a 10% acetone solution of 0.5 part of a styrene-methyl methacrylate-acrylic acid (80: 15: 5) copolymer was added using a fluidized bed coating apparatus. The coated spherical magnetic particle-dispersed carrier according to the present invention was obtained by coating.
比較例2 比較例1で得られたキャリヤ粒子100部に対し、スチ
レン−メタクリル酸メチル−アクリル酸(80:15:5)共
重合体0.5部を実施例3と同様の方法でコーティング
し、コート型球形磁性粒子分散型キャリヤを得た。Comparative Example 2 100 parts of the carrier particles obtained in Comparative Example 1 were coated with 0.5 part of a styrene-methyl methacrylate-acrylic acid (80: 15: 5) copolymer in the same manner as in Example 3 to coat the particles. A spherical magnetic particle dispersed carrier was obtained.
実施例1、2、3および比較例1、2で得たキャリヤ
を現像剤として評価した。トナーとしてはスチレン−ア
クリル樹脂とカーボンブラックからなる平均粒径11μの
FX−7770複写機用トナー(富士ゼロックス社製)を用
い、濃度が3重量%となる割合でキャリヤと混合して現
像剤とした。The carriers obtained in Examples 1, 2, 3 and Comparative Examples 1, 2 were evaluated as developers. The toner has an average particle size of 11μ composed of styrene-acrylic resin and carbon black.
A toner for FX-7770 copying machine (manufactured by Fuji Xerox Co., Ltd.) was mixed with a carrier at a concentration of 3% by weight to prepare a developer.
これらの現像剤について、感光体速度350mm/sec及び
現像磁気ロール(スリーブ)速度550mm/secとして、評
価用ベンチマシーンで初期の帯電量、ソリッド画像濃
度、背景部汚れ、細線再現性および感光体へのキャリヤ
の付着性、および10万枚ランニング時の帯電量、ソリッ
ド画像濃度、背景汚れ、細線再現性等を評価し、更に高
湿(30℃、80%R.H.)及び低湿(10℃、30%R.H.)環境
条件でもテストを行なった。その結果は次表に示すとお
りであり、本発明に係るキャリヤの優秀さが明らかとな
った。For these developers, the photoconductor speed was 350 mm / sec and the developing magnetic roll (sleeve) speed was 550 mm / sec, and the initial charge amount, solid image density, background stain, fine line reproducibility, and fine line reproducibility on the bench machine for evaluation. The carrier adhesion, the charge amount during running 100,000 sheets, the solid image density, the background stain, the fine line reproducibility, etc. were evaluated, and the high humidity (30 ° C, 80% RH) and low humidity (10 ° C, 30% RH) Tested under environmental conditions. The results are shown in the following table, and the superiority of the carrier according to the present invention was clarified.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 松村 保雄 神奈川県南足柄市竹松1600番地 富士ゼロ ックス株式会社竹松事業所内 (72)発明者 青木 孝義 神奈川県南足柄市竹松1600番地 富士ゼロ ックス株式会社竹松事業所内 (56)参考文献 特開 昭61−32860(JP,A) 特開 昭61−15157(JP,A) 特開 昭61−9665(JP,A) 特開 昭61−5255(JP,A) 特開 昭61−9658(JP,A) 特開 昭59−174857(JP,A) 特開 昭57−201247(JP,A) ─────────────────────────────────────────────────── --- Continuation of the front page (72) Inventor Yasuo Matsumura 1600 Takematsu, Minamiashigara City, Kanagawa Prefecture Fuji Xerox Co., Ltd. Takematsu Plant (72) Inventor Takayoshi Aoki 1600 Takematsu, Minami Ashigara City, Kanagawa Prefecture Fuji Xerox Co., Ltd. Takematsu Business In-house (56) References JP-A 61-32860 (JP, A) JP-A 61-15157 (JP, A) JP-A 61-9665 (JP, A) JP-A 61-5255 (JP, A) JP 61-9658 (JP, A) JP 59-174857 (JP, A) JP 57-201247 (JP, A)
Claims (1)
結着樹脂と磁性粉を必須成分とするキャリア材料溶融物
を噴霧冷却することにより得られる平均粒径が20〜400
μmであることを特徴とする現像剤用キャリア。1. An average particle size of 20 to 400 obtained by spray-cooling a binder resin containing a polyolefin having a functional group and a melt of a carrier material containing magnetic powder as essential components.
A carrier for a developer, which has a thickness of μm.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62014078A JPH0833684B2 (en) | 1987-01-26 | 1987-01-26 | Carrier for developer |
| US07/496,138 US5110703A (en) | 1987-01-26 | 1990-03-19 | Carrier for developer |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62014078A JPH0833684B2 (en) | 1987-01-26 | 1987-01-26 | Carrier for developer |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS63182666A JPS63182666A (en) | 1988-07-27 |
| JPH0833684B2 true JPH0833684B2 (en) | 1996-03-29 |
Family
ID=11851072
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP62014078A Expired - Lifetime JPH0833684B2 (en) | 1987-01-26 | 1987-01-26 | Carrier for developer |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0833684B2 (en) |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57201247A (en) * | 1981-06-05 | 1982-12-09 | Canon Inc | Toner |
| JPS59174857A (en) * | 1983-03-24 | 1984-10-03 | Pilot Pen Co Ltd:The | Manufacture of pressure-fixable magnetic toner |
| JPS615255A (en) * | 1984-06-20 | 1986-01-11 | Konishiroku Photo Ind Co Ltd | Image forming method |
| JPS619665A (en) * | 1984-06-25 | 1986-01-17 | Konishiroku Photo Ind Co Ltd | Magnetic powder dispersed type microcarrier |
| JPS619658A (en) * | 1984-06-25 | 1986-01-17 | Konishiroku Photo Ind Co Ltd | Formation of image |
| JPS6115157A (en) * | 1984-06-30 | 1986-01-23 | Konishiroku Photo Ind Co Ltd | Formation of image |
| JPS6132860A (en) * | 1984-07-25 | 1986-02-15 | Konishiroku Photo Ind Co Ltd | Image forming method |
-
1987
- 1987-01-26 JP JP62014078A patent/JPH0833684B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPS63182666A (en) | 1988-07-27 |
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