JPH0456983B2 - - Google Patents
Info
- Publication number
- JPH0456983B2 JPH0456983B2 JP59041831A JP4183184A JPH0456983B2 JP H0456983 B2 JPH0456983 B2 JP H0456983B2 JP 59041831 A JP59041831 A JP 59041831A JP 4183184 A JP4183184 A JP 4183184A JP H0456983 B2 JPH0456983 B2 JP H0456983B2
- Authority
- JP
- Japan
- Prior art keywords
- carrier
- magnetic
- powder
- magnetization
- styrene
- 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
- 239000000843 powder Substances 0.000 claims description 19
- 229920005989 resin Polymers 0.000 claims description 19
- 239000011347 resin Substances 0.000 claims description 19
- 239000002245 particle Substances 0.000 claims description 16
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 15
- 238000011161 development Methods 0.000 claims description 9
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims description 8
- 239000011230 binding agent Substances 0.000 claims description 6
- 229910052742 iron Inorganic materials 0.000 claims description 5
- 239000002184 metal Substances 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000011248 coating agent Substances 0.000 claims 1
- 238000000576 coating method Methods 0.000 claims 1
- 230000005415 magnetization Effects 0.000 description 19
- 229920001577 copolymer Polymers 0.000 description 10
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 108091008695 photoreceptors Proteins 0.000 description 7
- 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
- 238000004519 manufacturing process Methods 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- -1 polyP-chlorostyrene Polymers 0.000 description 3
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 3
- 239000006229 carbon black Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000011981 development test Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000004907 flux Effects 0.000 description 2
- UCNNJGDEJXIUCC-UHFFFAOYSA-L hydroxy(oxo)iron;iron Chemical compound [Fe].O[Fe]=O.O[Fe]=O UCNNJGDEJXIUCC-UHFFFAOYSA-L 0.000 description 2
- 239000006247 magnetic powder Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229920007962 Styrene Methyl Methacrylate Polymers 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000012050 conventional carrier Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000006249 magnetic particle Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- ADFPJHOAARPYLP-UHFFFAOYSA-N methyl 2-methylprop-2-enoate;styrene Chemical compound COC(=O)C(C)=C.C=CC1=CC=CC=C1 ADFPJHOAARPYLP-UHFFFAOYSA-N 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 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
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920002102 polyvinyl toluene Polymers 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 229920006249 styrenic copolymer Polymers 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000004416 thermosoftening plastic 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
- G03G9/10—Developers with toner particles characterised by carrier particles
- G03G9/107—Developers with toner particles characterised by carrier particles having magnetic components
- G03G9/1075—Structural characteristics of the carrier particles, e.g. shape or crystallographic structure
Landscapes
- Chemical & Material Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Developing Agents For Electrophotography (AREA)
Description
【発明の詳細な説明】
本発明は、電子写真現像剤用キヤリヤに関し、
更に詳しくは、磁性微粉末を樹脂中に分散させて
なる二成分系現像剤用キヤリヤに関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a carrier for an electrophotographic developer,
More specifically, the present invention relates to a carrier for a two-component developer in which fine magnetic powder is dispersed in a resin.
近年、二成分系磁気ブラシ現像剤用キヤリヤと
して、従来の大径(80μ〜200μ)の鉄粉などの代
りに0.1μ〜1.0μの磁性微粉末をバインダー樹脂に
分散させてなる小径(5μ〜40μ)の粒子を用いた
ものが実用に供されるようになつてきた。この種
の二成分系現像剤は、従来の鉄粉などのキヤリヤ
を用いたものに比べてキヤリヤの粒径が小さいこ
とから、複写画像の品質が良く、しかもキヤリヤ
とトナーの混合比の変動の許容幅が広いという利
点を有している。しかし、その反面、キヤリヤが
非常に小さいため現像時に、感光体上に形成され
た潜像の画像部や、画像部周辺に付着しやすく、
特に、はなはだしい場合には、付着したキヤリヤ
の一部が紙に転写され画像部周辺のチリとなつて
現れ、ひいてはキヤリヤの不足を招くという問題
があつた。 In recent years, as a carrier for two-component magnetic brush developers, instead of the conventional large diameter (80μ to 200μ) iron powder, etc., small diameter (5μ to 5μ), which is made by dispersing magnetic fine powder of 0.1μ to 1.0μ in binder resin, has been used as a carrier for two-component magnetic brush developers. 40μ) particles are now being put into practical use. This type of two-component developer has a smaller carrier particle size than conventional carriers such as iron powder, so the quality of the copied images is good, and the variation in the carrier to toner mixing ratio is less It has the advantage of wide tolerance. However, on the other hand, since the carrier is very small, it tends to adhere to the image area of the latent image formed on the photoreceptor or around the image area during development.
Particularly in cases where the amount of the carrier is too large, a portion of the adhered carrier is transferred to the paper and appears as dust around the image area, resulting in a problem of a shortage of carrier.
このキヤリヤの感光体への付着の問題は、襲来
より解析されており、基本的にはキヤリヤを感光
体側に引きつける静電気的な力と、磁気ロール側
に引きつける磁気的な力のバランスが崩れ、静電
気的な力が、磁気的な力を上まわつた場合に、感
光体への付着が生ずる。静電気的な力には、現像
時にキヤリヤに誘起される電荷も含めたキヤリヤ
の帯電量、現像条件である感光体の種類やバイア
ス電圧などが関係し、磁気的な力には、磁気ロー
ルの磁束密度やキヤリヤの磁化などが関係してい
ることが明らかにされてきている。 This problem of carrier adhesion to the photoreceptor has been analyzed since then, and basically, the balance between the electrostatic force that attracts the carrier to the photoreceptor side and the magnetic force that attracts it to the magnetic roll side is disrupted, resulting in static electricity. Adhesion to the photoreceptor occurs when the magnetic force exceeds the magnetic force. The electrostatic force is related to the amount of charge on the carrier, including the charge induced on the carrier during development, the type of photoreceptor used as the development condition, the bias voltage, etc., and the magnetic force is related to the magnetic flux of the magnetic roll. It has become clear that density and carrier magnetization are related.
そこで、キヤリヤ付着に対する種々の対策が考
えられるが、感光体の種類、バイアス電圧、磁気
ロールの磁束密度などの現像条件に関すること
は、システムの構成上容易には変えることは困難
であり、キヤリヤの帯電量なども現像剤の全体的
な設計の上から、容易に変えられない。また、ト
ナーにシリカを添加することが提案(特開昭56−
62256)されているが、この方法では、それほど
大きな効果は期待できない。さらに、シリカ添加
によるフイルム・フオーミングなどの悪影響もあ
る。 Therefore, various measures can be taken to prevent carrier adhesion, but it is difficult to easily change development conditions such as the type of photoconductor, bias voltage, and magnetic flux density of the magnetic roll due to the system configuration. The amount of charge cannot be easily changed due to the overall design of the developer. Also, it was proposed to add silica to toner (Japanese Patent Application Laid-Open No. 1983-
62256), but this method cannot be expected to have much of an effect. Furthermore, there are also negative effects such as film forming due to the addition of silica.
このような状況にあつて、キヤリヤ付着の対策
に最も効果のある方法は、キヤリヤの磁化を高め
ることである。このためには、(1)キヤリヤの磁化
を大きくすること。(2)特に、樹脂中に磁性微粉末
を分散してなる磁性粉分散型樹脂キヤリヤにおい
ては、磁性微粉末の含有量を増すると、(3)磁化の
高い磁性微粉末を使用すること、の三つの方法が
考えられる。しかし、これらのうち(1)と(2)の方法
は、キヤリヤの平均粒径が50μを超えれば、現像
剤としての特徴が失われるし、また、樹脂中に混
練できる磁性微粉末の量には、自から限界がある
ので、その効果にも限度がある。(3)の方法はキヤ
リヤ付着の対策として有望であると考えられる
が、現在までのところ、この目的に合つた適当な
材料が見出されていない。即ち、通常使用されて
いるマグネタイトでは、1Kエルステツドの磁場
中の磁化は、一般に期待される最大の磁化でも
65emu/gr程度であり、それ以上の磁化を得る
ことは不可能である。マグネタイトに代えて、粒
径0.1μ〜1.0μの鉄粉を用いれば、磁化を65emu/
gr以上に高めることは可能であるが、鉄粉は、
きわめて不安定であり、製造上の危険があるた
め、通常の方法では製造が困難であり、製造工程
はかなり複雑でコストの高いものとなることが予
想されるので、これを用いることも現実的でなな
い。 Under such circumstances, the most effective method to prevent carrier adhesion is to increase the magnetization of the carrier. To achieve this, (1) increase the magnetization of the carrier; (2) In particular, in magnetic powder-dispersed resin carriers made by dispersing magnetic fine powder in resin, increasing the content of magnetic fine powder will (3) use magnetic fine powder with high magnetization; Three methods are possible. However, in methods (1) and (2), if the average particle size of the carrier exceeds 50μ, it loses its characteristics as a developer, and the amount of magnetic fine powder that can be mixed into the resin is limited. has its own limits, so there are limits to its effectiveness. Method (3) is considered to be promising as a countermeasure against carrier adhesion, but so far no material suitable for this purpose has been found. In other words, for the normally used magnetite, the magnetization in a magnetic field of 1K oersted is the maximum magnetization that is generally expected.
The magnetization is about 65 emu/gr, and it is impossible to obtain magnetization higher than that. If iron powder with a particle size of 0.1μ to 1.0μ is used instead of magnetite, the magnetization can be reduced to 65emu/
Although it is possible to increase the gr
It is difficult to manufacture using normal methods because it is extremely unstable and has manufacturing risks, and the manufacturing process is expected to be quite complex and expensive, so it is not practical to use this method. It's not.
従つて、本発明の目的はキヤリヤの感光体への
付着を防止するための高い磁化をもつ磁性粉分散
型樹脂キヤリヤを提供することにある。 SUMMARY OF THE INVENTION Accordingly, an object of the present invention is to provide a magnetic powder-dispersed resin carrier having high magnetization to prevent the carrier from adhering to a photoreceptor.
本発明の他の目的は、マグネタイトなどよりも
高い磁化をもつ金属鉄を含む磁性微粉末を使用
し、通常の製造方法で安全に製造し得る磁性粉分
散型樹脂キヤリヤを提供することにある。 Another object of the present invention is to provide a magnetic powder-dispersed resin carrier that can be safely manufactured by a conventional manufacturing method using magnetic fine powder containing metal iron having higher magnetization than magnetite or the like.
これらの目的を達成する本発明の電子写真現像
用磁性粉分散型樹脂キヤリヤは、金属鉄と鉄の酸
化物の重合割合が25:75〜85:15となるように金
属鉄の芯の表面を鉄の酸化物で被覆して成る磁性
微粉末を絶縁性バインダー中に分散させて成り、
平均粒径が10〜35μであることを特徴とするもの
である。 The magnetic powder-dispersed resin carrier for electrophotographic development of the present invention, which achieves these objectives, has a surface of a metal iron core such that the polymerization ratio of metal iron and iron oxide is 25:75 to 85:15. It is made by dispersing magnetic fine powder coated with iron oxide in an insulating binder.
It is characterized by an average particle size of 10 to 35μ.
磁性微粉末の粒径は、平均粒径で0.1〜1.0μが
適当である。このような磁性微粉末の磁化は1K
エルステツドの磁場の中で70emu/gr以上であ
り、その保磁力は70〜300エルステツドである。
このような磁化と保磁力の値は、キヤリヤの感光
体への付着を防止するのに充分なものである。 The average particle size of the magnetic fine powder is suitably 0.1 to 1.0μ. The magnetization of such magnetic fine powder is 1K
It is more than 70 emu/gr in the Oersted magnetic field, and its coercive force is 70 to 300 Oersted.
These magnetization and coercivity values are sufficient to prevent the carrier from sticking to the photoreceptor.
絶縁性バインダー樹脂としては、例えばポリス
チレン、ポリP−クロルスチレン、ポリビニルト
ルエンなどのスチレン又はその置換体の単独重合
体、スチレン−P−クロルスチレン共重合体、ス
チレン−プロピレン共重合体、スチレン−ビニル
トルエン共重合体、スチレン−ビニルナフタリン
共重合体、スチレン−アクリル酸メチル共重合
体、スチレン−アクリル酸エチル共重合体、スチ
レン−アクリル酸ブチル共重合体、スチレン−メ
タアクリル酸メチル共重合体、スチレン−メタア
クリル酸エチル共重合体、スチレン−メタアクリ
ル酸ブチル共重合体、スチレン−アクリロニトル
共重合体、スチレン−ブタジエン共重合体、スチ
レン−イソプレン共重合体などのスチレン系共重
合体;ポリメチルメタクリレート、ポリ塩化ビニ
ル、ポリエチレン、ポリプロピレン、熱可塑性ポ
リエステル、ポリウレタンなどの熱可塑性樹脂の
他、変性アクリル樹脂、フエノール樹脂、メラミ
ン樹脂、ユリア樹脂などの熱硬化性樹脂を使用で
きる。 Examples of the insulating binder resin include homopolymers of styrene or substituted products thereof such as polystyrene, polyP-chlorostyrene, and polyvinyltoluene, styrene-P-chlorostyrene copolymers, styrene-propylene copolymers, and styrene-vinyl Toluene copolymer, styrene-vinylnaphthalene copolymer, styrene-methyl acrylate copolymer, styrene-ethyl acrylate copolymer, styrene-butyl acrylate copolymer, styrene-methyl methacrylate copolymer, Styrenic copolymers such as styrene-ethyl methacrylate copolymer, styrene-butyl methacrylate copolymer, styrene-acrylonitrile copolymer, styrene-butadiene copolymer, and styrene-isoprene copolymer; polymethyl In addition to thermoplastic resins such as methacrylate, polyvinyl chloride, polyethylene, polypropylene, thermoplastic polyester, and polyurethane, thermosetting resins such as modified acrylic resins, phenolic resins, melamine resins, and urea resins can be used.
磁性微粉末と絶縁性バインダーの配合割合は、
絶縁性バインダー樹脂100重量部に対して磁性微
粉末80〜400重量部が適当である。 The blending ratio of magnetic fine powder and insulating binder is
It is appropriate to use 80 to 400 parts by weight of the magnetic fine powder per 100 parts by weight of the insulating binder resin.
本発明のキヤリヤは、上記二成分のほかに、必
要に応じて更に顔料・染料の如き着色剤、抵抗制
御剤、帯電制御剤の如き助剤等を含有し、また本
発明の目的を害さない範囲でマグネタイトの如き
他の磁性微粉末を含有してもよい。 In addition to the above two components, the carrier of the present invention further contains coloring agents such as pigments and dyes, auxiliary agents such as resistance control agents and charge control agents, etc., and does not impede the purpose of the present invention. It may also contain other magnetic fine powders such as magnetite.
本発明のキヤリヤは、上記成分の混合物を熔融
混練し、粉砕し、分級することにより製造され
る。キヤリヤの平均粒径は、10〜35μ、好ましく
は15〜30μが適当である。 The carrier of the present invention is produced by melt-kneading, pulverizing, and classifying a mixture of the above components. The average particle size of the carrier is suitably 10-35μ, preferably 15-30μ.
以下、実施例と比較例により本発明を更に具体
的に説明する。 Hereinafter, the present invention will be explained in more detail with reference to Examples and Comparative Examples.
各例中の「部」及び「%」は夫々「重量部」お
よび「重量%」を意味する。 "Parts" and "%" in each example mean "parts by weight" and "% by weight," respectively.
実施例 1
スチレン−アクリル共重合体 100部
(三洋化成社製、「ハイマーSBM73〕)
磁性微粉末 200部
同和鉄粉社製、 「MR−20」
金属鉄含有量 28.2%
1Kエルステツドの磁場中での磁化
70emu/gr
保磁力 110エルステツド
粉径 0.2μ〜0.8μ
上記組成の混合物をニーダーで熔融混練し、冷
却後、粉砕し、分級して平均粒径23μの磁性粉分
散型樹脂キヤリヤを得た。このキヤリヤの1Kエ
ルステツドの磁場中での磁化は、47emu/gr、
保磁力は110エルステツド抵抗は9×1012Ω−cm
であつた。Example 1 Styrene-acrylic copolymer 100 parts (manufactured by Sanyo Kasei Co., Ltd., "HIMER SBM73") Magnetic fine powder 200 parts Manufactured by Dowa Iron Powder Co., Ltd., "MR-20" Metallic iron content 28.2% In a magnetic field of 1 K oersted magnetization of
70 emu/gr Coercive force 110 oersted Powder diameter 0.2 μm to 0.8 μm The mixture having the above composition was melt-kneaded in a kneader, cooled, pulverized, and classified to obtain a magnetic powder-dispersed resin carrier having an average particle size of 23 μm. The magnetization of this carrier in a 1K oersted magnetic field is 47emu/gr.
Coercive force is 110 Oersted resistance is 9×10 12 Ω-cm
It was hot.
これとは別に、スチレン樹脂(エツソ化学社
製、「ピコラスチツクD−125」)100部、カーボン
ブラツク(キヤボツト社製、「エルフテツク8」)
10部、および染料(オリエント化学社製、「オイ
ルブラツク B2」2部をニーダーで熔融混練し、
冷却後、粉砕し、分級して平均粒径12μのトナー
を得た。 Separately, 100 parts of styrene resin (manufactured by Etsuo Kagaku Co., Ltd., "Picolastik D-125"), carbon black (manufactured by Kabot Corporation, "Elftek 8")
Melt and knead 10 parts and 2 parts of dye ("Oil Black B2" manufactured by Orient Chemical Co., Ltd.) in a kneader,
After cooling, it was crushed and classified to obtain a toner with an average particle size of 12μ.
このようにして得られたキヤリヤとトナーを
90:10の割合で混合して二成分系現像剤を調整
し、この現像剤を用いて磁気刷子現像装置を備え
た電子写真複写機により現像を行つた。その結
果、画像部周辺および画像部のいずれにもキヤリ
ヤ付着は全く認められず、優れた画質の複写画像
が得られた。 The carrier and toner obtained in this way are
A two-component developer was prepared by mixing at a ratio of 90:10, and development was carried out using an electrophotographic copying machine equipped with a magnetic brush developing device. As a result, no carrier adhesion was observed in or around the image area, and a copy image of excellent quality was obtained.
比較例 1
実施例1の磁性微粉末をマグネタイト(チタン
工業社製、「RB−BL」、1Kエルステツドの磁場
中での磁化49emu/gr、保磁力220エルステツ
ド)に代えた以外は実施例1と同様の方法で、平
均粒径25μの磁性粉分散型樹脂キヤリヤを得た。
このキヤリヤの1Kエルステツドの磁場での磁化
は33emu/gr、保磁力は220エルステツド、抵
抗は、2×1013Ω−cmであつた。Comparative Example 1 Same as Example 1 except that the magnetic fine powder of Example 1 was replaced with magnetite (manufactured by Titan Kogyo Co., Ltd., "RB-BL", magnetization 49 emu/gr in a 1K Oersted magnetic field, coercive force 220 Oersted). A magnetic powder-dispersed resin carrier having an average particle size of 25 μm was obtained in the same manner.
The magnetization of this carrier in a magnetic field of 1 K Oersted was 33 emu/gr, the coercive force was 220 Oersted, and the resistance was 2×10 13 Ω-cm.
このキヤリヤを用いて、実施例1と同様の方法
で現像テストを行つた。この結果、得られた画像
は、画像部周辺にキヤリヤの付着した劣悪なもの
であつた。 Using this carrier, a development test was conducted in the same manner as in Example 1. As a result, the resulting image was of poor quality with carrier adhering to the periphery of the image area.
実施例 2
スチレン−アクリル共重合体 100部
(「ハイアーSBM」 73)
磁性微粉末 100部
同和鉄粉社製、「MR−25」
金属鉄含有量 53%
1Kエルステツドの磁場中での磁化
80emu/gr
保磁力 100エルステツド
粉径 0.2μ〜0.8μ
マグネタイト 100部
(チタン工業社製、「RB−BL」)
上記組成の混合物を用いて実施例1と同様の方
法で平均粒径24μの磁性粉分散型樹脂キヤリヤを
得た。このキヤリヤの1Kエルステツドの磁場中
での磁化は43emu/gr、保磁力は160エルステ
ツド、抵抗は1×1013Ω−cmであつた。Example 2 Styrene-acrylic copolymer 100 parts ("Higher SBM" 73) Magnetic fine powder 100 parts "MR-25" manufactured by Dowa Iron Powder Co., Ltd. Metallic iron content 53% Magnetization in a 1K Oersted magnetic field
80 emu/gr Coercive force 100 oersted Powder size 0.2 μ to 0.8 μ Magnetite 100 parts (manufactured by Titan Kogyo Co., Ltd., “RB-BL”) Using a mixture with the above composition, magnetic particles with an average particle size of 24 μ were prepared in the same manner as in Example 1. A powder-dispersed resin carrier was obtained. The magnetization of this carrier in a 1K Oersted magnetic field was 43 emu/gr, the coercive force was 160 Oersted, and the resistance was 1×10 13 Ω-cm.
この磁性粉分散型樹脂キヤリヤと実施例1で説
明したトーナーを90:10の割合で混合して現像剤
を調整し、この現像剤を用いて実施例1と同様の
方法で現像した。その結果、画像部周辺および画
像部のいずれにもキヤリヤ付着は認められず、優
れた画質の複写画像が得られた。 A developer was prepared by mixing this magnetic powder dispersed resin carrier and the toner described in Example 1 at a ratio of 90:10, and development was carried out in the same manner as in Example 1 using this developer. As a result, no carrier adhesion was observed either around the image area or in the image area, and a copied image of excellent image quality was obtained.
実施例 3
実施例1の組成にカーボンブラツク(キヤボツ
ト社製、「XC−72」を6部加えるほかは同様にし
て平均粒径29μの磁性粉分散型樹脂キヤリヤを得
た。このキヤリヤの抵抗は5×109Ω−cmであつ
た。Example 3 A magnetic powder-dispersed resin carrier with an average particle size of 29 μm was obtained in the same manner as in Example 1 except that 6 parts of carbon black (manufactured by CABOT Co., Ltd., “XC-72” was added. The resistance of this carrier was It was 5×10 9 Ω-cm.
このキヤリヤを用いて、実施例1と同様の方法
で現像テストを行つた。 Using this carrier, a development test was conducted in the same manner as in Example 1.
その結果、画像部周辺および画像部のいずれに
もキヤリヤ付着は認められず、優れた画質の複写
画像が得られた。 As a result, no carrier adhesion was observed either around the image area or in the image area, and a copied image of excellent image quality was obtained.
実施例 4
実施例1の組成に染料(オリエント化学社製、
「スピリツトブラツク SB」)を6部加え、ニー
ダーで熔融混練し、冷却後、粉砕し、分級して平
均粒径35μの磁性粉分散型樹脂キヤリヤを得た。Example 4 A dye (manufactured by Orient Chemical Co., Ltd.,
6 parts of "Spirit Black SB") were added, melted and kneaded in a kneader, cooled, pulverized, and classified to obtain a magnetic powder-dispersed resin carrier with an average particle size of 35 μm.
これとは別に、下記組成の混合物を熔融混練
し、冷却後、粉砕し、分級して、平均粒径11.0μ
の磁性トナーを得た。 Separately, a mixture with the following composition was melt-kneaded, cooled, crushed, and classified to have an average particle size of 11.0μ.
A magnetic toner was obtained.
スチレン−アクリル共重合体 100重量部
(三洋化成社製、「ハイマー SBM 700」)
マグネタイト 70重量部
(チタン工業社製、「BL−100」)
上記キヤリヤと磁性トナーを80:20の割合で混
合して現像剤を調整し、この現像剤を用いて正電
荷潜像を現像する磁気刷子現像装置を備えた電子
写真複写機により現像を行つた。 Styrene-acrylic copolymer 100 parts by weight (manufactured by Sanyo Kasei Co., Ltd., "Himer SBM 700") Magnetite 70 parts by weight (manufactured by Titan Kogyo Co., Ltd., "BL-100") The above carrier and magnetic toner were mixed in a ratio of 80:20. A developer was prepared using this developer, and development was carried out using an electrophotographic copying machine equipped with a magnetic brush developing device for developing a positively charged latent image.
その結果、画像部周辺および画像部のいずれに
もキヤリヤの付着は認められず、優れた画質の複
写画像が得られた。 As a result, no carrier adhesion was observed either around the image area or in the image area, and a copy image of excellent quality was obtained.
Claims (1)
85:15となるように金属鉄の芯の表面を鉄の酸化
物で被覆して成る磁性微粉末を絶縁性バインダー
中に分散させて成り、平均粒径が10〜35μである
ことを特徴とする電子写真現像用磁性粉分散型樹
脂キヤリヤ。 2 磁性微粉末の平均粒径が0.1〜1.0μである特
許請求の範囲第1項のキヤリヤ。[Claims] 1. The weight ratio of metallic iron and iron oxide is 25:75 to 25:75.
It is made by dispersing magnetic fine powder, which is made by coating the surface of a metal iron core with iron oxide in a ratio of 85:15, in an insulating binder, and has an average particle size of 10 to 35μ. A magnetic powder-dispersed resin carrier for electrophotographic development. 2. The carrier according to claim 1, wherein the magnetic fine powder has an average particle size of 0.1 to 1.0μ.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59041831A JPS60185961A (en) | 1984-03-05 | 1984-03-05 | Carrier of electrophotographic developer |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59041831A JPS60185961A (en) | 1984-03-05 | 1984-03-05 | Carrier of electrophotographic developer |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS60185961A JPS60185961A (en) | 1985-09-21 |
JPH0456983B2 true JPH0456983B2 (en) | 1992-09-10 |
Family
ID=12619209
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP59041831A Granted JPS60185961A (en) | 1984-03-05 | 1984-03-05 | Carrier of electrophotographic developer |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60185961A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0690541B2 (en) * | 1986-07-10 | 1994-11-14 | ミノルタ株式会社 | Binder type carrier |
US5108862A (en) * | 1989-02-21 | 1992-04-28 | Toda Kogyo Corp. | Composite carrier particles for electrophotography and process for producing the same |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5515121A (en) * | 1978-07-19 | 1980-02-02 | Ricoh Co Ltd | Carrier particle for electrostatic image developer |
JPS5532073A (en) * | 1978-08-28 | 1980-03-06 | Minolta Camera Co Ltd | Electrophotographic developing method |
JPS5650337A (en) * | 1979-09-29 | 1981-05-07 | Nippon Teppun Kk | Resin coated carrier |
JPS5651755A (en) * | 1979-10-03 | 1981-05-09 | Minolta Camera Co Ltd | Magnetic particle for electrophotographic developer |
JPS58136052A (en) * | 1982-02-08 | 1983-08-12 | Minolta Camera Co Ltd | Magnetic developer |
JPS5922055A (en) * | 1982-07-06 | 1984-02-04 | ゼロツクス・コ−ポレ−シヨン | Treatment of surface of steel carrier core |
JPS5997156A (en) * | 1982-11-26 | 1984-06-04 | Konishiroku Photo Ind Co Ltd | Electrostatic image developing carrier |
-
1984
- 1984-03-05 JP JP59041831A patent/JPS60185961A/en active Granted
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5515121A (en) * | 1978-07-19 | 1980-02-02 | Ricoh Co Ltd | Carrier particle for electrostatic image developer |
JPS5532073A (en) * | 1978-08-28 | 1980-03-06 | Minolta Camera Co Ltd | Electrophotographic developing method |
JPS5650337A (en) * | 1979-09-29 | 1981-05-07 | Nippon Teppun Kk | Resin coated carrier |
JPS5651755A (en) * | 1979-10-03 | 1981-05-09 | Minolta Camera Co Ltd | Magnetic particle for electrophotographic developer |
JPS58136052A (en) * | 1982-02-08 | 1983-08-12 | Minolta Camera Co Ltd | Magnetic developer |
JPS5922055A (en) * | 1982-07-06 | 1984-02-04 | ゼロツクス・コ−ポレ−シヨン | Treatment of surface of steel carrier core |
JPS5997156A (en) * | 1982-11-26 | 1984-06-04 | Konishiroku Photo Ind Co Ltd | Electrostatic image developing carrier |
Also Published As
Publication number | Publication date |
---|---|
JPS60185961A (en) | 1985-09-21 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPH05273789A (en) | Electrophotographic developer | |
JPH0140977B2 (en) | ||
US4599289A (en) | Pressure-fixable encapsulated toner | |
JPH0330855B2 (en) | ||
US4262076A (en) | Method for manufacturing magnetically attractive toner particles and particle | |
JPH0330856B2 (en) | ||
JPH0456983B2 (en) | ||
JPH027062B2 (en) | ||
JPH0259982B2 (en) | ||
JPS6342778B2 (en) | ||
JPS63228174A (en) | Magnetic carrier and its manufacture | |
JPH0451249A (en) | Magnetic toner and production thereof | |
JP3104487B2 (en) | Positively chargeable toner and two-component developer | |
JPH0257302B2 (en) | ||
JP2855852B2 (en) | Electrophotography | |
JP2808776B2 (en) | Thermal fixing type magnetic toner for developing magnetic latent images | |
JPH0368956A (en) | Toner for electrophotography | |
JPH02137855A (en) | Toner for development of electrostatic image | |
JPS6026351A (en) | Magnetic toner | |
JPH0623868B2 (en) | Reverse development method | |
JP2567748B2 (en) | Toner for electrostatic charge development | |
JP2831870B2 (en) | Development method | |
JPS63257764A (en) | Magnetic toner | |
JPS597379B2 (en) | magnetic toner | |
JPH01297660A (en) | Magnetic toner |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
LAPS | Cancellation because of no payment of annual fees |