JPH0719079B2 - Carrier particles for electrostatic image development - Google Patents
Carrier particles for electrostatic image developmentInfo
- Publication number
- JPH0719079B2 JPH0719079B2 JP58098810A JP9881083A JPH0719079B2 JP H0719079 B2 JPH0719079 B2 JP H0719079B2 JP 58098810 A JP58098810 A JP 58098810A JP 9881083 A JP9881083 A JP 9881083A JP H0719079 B2 JPH0719079 B2 JP H0719079B2
- Authority
- JP
- Japan
- Prior art keywords
- carrier
- carrier particles
- present
- silane compound
- particles
- 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
- 239000002245 particle Substances 0.000 title claims description 19
- -1 silane compound Chemical class 0.000 claims description 19
- 229910000077 silane Inorganic materials 0.000 claims description 14
- 125000001302 tertiary amino group Chemical group 0.000 claims description 9
- 239000007771 core particle Substances 0.000 claims description 6
- 239000011247 coating layer Substances 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 239000011162 core material Substances 0.000 description 12
- 238000000034 method Methods 0.000 description 10
- 239000011248 coating agent Substances 0.000 description 8
- 238000000576 coating method Methods 0.000 description 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 229910000859 α-Fe Inorganic materials 0.000 description 6
- 239000000969 carrier Substances 0.000 description 5
- 238000001035 drying Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 239000011362 coarse particle Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000007873 sieving Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 229910003962 NiZn Inorganic materials 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 229940090961 chromium dioxide Drugs 0.000 description 1
- IAQWMWUKBQPOIY-UHFFFAOYSA-N chromium(4+);oxygen(2-) Chemical compound [O-2].[O-2].[Cr+4] IAQWMWUKBQPOIY-UHFFFAOYSA-N 0.000 description 1
- AYTAKQFHWFYBMA-UHFFFAOYSA-N chromium(IV) oxide Inorganic materials O=[Cr]=O AYTAKQFHWFYBMA-UHFFFAOYSA-N 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000004807 desolvation Methods 0.000 description 1
- YQGOWXYZDLJBFL-UHFFFAOYSA-N dimethoxysilane Chemical compound CO[SiH2]OC YQGOWXYZDLJBFL-UHFFFAOYSA-N 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- CGOQMMFKARADST-UHFFFAOYSA-N n-ethyl-n-(3-trimethoxysilylpropyl)aniline Chemical compound CO[Si](OC)(OC)CCCN(CC)C1=CC=CC=C1 CGOQMMFKARADST-UHFFFAOYSA-N 0.000 description 1
- DTPZJXALAREFEY-UHFFFAOYSA-N n-methyl-3-triethoxysilylpropan-1-amine Chemical compound CCO[Si](OCC)(OCC)CCCNC DTPZJXALAREFEY-UHFFFAOYSA-N 0.000 description 1
- KZOFPGJROZQQRZ-UHFFFAOYSA-N n-methyl-n-(3-trimethoxysilylpropyl)aniline Chemical compound CO[Si](OC)(OC)CCCN(C)C1=CC=CC=C1 KZOFPGJROZQQRZ-UHFFFAOYSA-N 0.000 description 1
- ADMSYFDHHJCVGQ-UHFFFAOYSA-N n-methyl-n-(4-triethoxysilylbutyl)aniline Chemical compound CCO[Si](OCC)(OCC)CCCCN(C)C1=CC=CC=C1 ADMSYFDHHJCVGQ-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 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
- G03G9/113—Developers with toner particles characterised by carrier particles having coatings applied thereto
- G03G9/1138—Non-macromolecular organic components of coatings
Landscapes
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (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、静電記録法において静電潜像の現
像のために使用する静電荷像現像用キヤリヤ粒子に関す
る。更に詳細にはコアと被覆樹脂とからなる高耐久性を
有する静電荷像現像用キヤリヤ粒子を提供するものであ
る。TECHNICAL FIELD The present invention relates to a carrier particle for developing an electrostatic charge image, which is used for developing an electrostatic latent image in electrophotography and electrostatic recording. More specifically, the present invention provides a carrier particle for developing an electrostatic charge image, which comprises a core and a coating resin and has high durability.
従来技術 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等を用いてト
ナーを付着して顕像化させる方式が一般的に使用されて
いる。In the conventional electrophotographic method, a photoconductive substance such as selenium is used as a photoconductor, an electric latent image is formed by various means, and a toner is formed on the latent image by a magnetic brush development method or the like. A method of adhering and visualizing is generally used.
この現像工程において、トナーに適当量の正または負の
電気量を付与する為にキヤリヤと呼ばれる担体粒子が使
用される。キヤリヤはコートキヤリヤと非コートキヤリ
ヤとに大別される。しかしながら、現像剤寿命等を考慮
した場合にはコートキヤリヤの方が優れているので、種
々のタイプのコートキヤリヤが開発されかつ実用化され
ている。In this developing step, carrier particles called carriers are used in order to give an appropriate amount of positive or negative amount of electricity to the toner. Carriers are roughly classified into coated carriers and non-coated carriers. However, since the coat carrier is superior in consideration of the life of the developer, various types of coat carriers have been developed and put into practical use.
このコートキヤリヤに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(芯材料)と被覆材料との良好な密着性等を挙
げることができる。There are various characteristics required for this coat carrier, and as particularly important characteristics, suitable charging property, impact resistance, abrasion resistance, good adhesion between the core (core material) and the coating material, and the like are mentioned. it can.
上記諸要求特性を考慮すると、従来使用されてきたコー
トキヤリヤは依然として改善すべき問題を残しており、
完全なものはいまのところ知られていない。例えば、フ
ツ素化ビニルポリマー類は帯電性において優れている
が、コア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、コアとの密着性の点では満
足できるものの、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 required characteristics, the conventionally used coat carrier still has a problem to be improved,
The complete one is not known so far. For example, fluorinated vinyl polymers are excellent in chargeability, but have problems in adhesion to the core, and acrylic polymers are satisfactory in mechanical strength and adhesion to the core It is said that there is a problem with sex. In any case, it is the current situation that the use of coating materials having advantages and disadvantages is unavoidable.
発明の目的 このような現状に鑑みて、本発明者等は前記従来製品の
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ヤリヤの諸要求特性
の改良において有効であることを見出し、本発明を完成
するに至つた。OBJECTS OF THE INVENTION In view of such a current situation, the inventors of the present invention have conducted various studies and studies to improve the drawbacks of the conventional products, and as a result, it has been found that the use of a specific coating material can improve various required characteristics of the coat carrier. The inventors have found that it is effective and have completed the present invention.
そこで、本発明の主な目的は上記従来製品の欠点を克服
したキヤリヤを提供することにある。Therefore, a main object of the present invention is to provide a carrier that overcomes the drawbacks of the conventional products.
本発明の他の目的は、特に正の帯電性に優れ、被覆によ
るコアの電気抵抗の変化が小さく、更に温、湿度依存性
の低いコートキヤリヤを提供することにある。Another object of the present invention is to provide a coat carrier which is particularly excellent in positive charging property, has a small change in electric resistance of the core due to coating, and has low temperature and humidity dependency.
発明の構成 本発明の前記並びにその他の目的はコア材料を三級アミ
ノ基含有シラン化合物で処理することによつて達成する
ことができる。SUMMARY OF THE INVENTION The above and other objects of the present invention can be achieved by treating a core material with a tertiary amino group-containing silane compound.
即ち、本発明はコア粒子と、その上の三級アミノ基含有
シラン化合物の被覆層とを含み、該三級アミノ基が窒素
原子にフェニル基かつ低級アルキル基が結合してなるこ
とを特徴とする静電荷像現像用キャリヤ粒子 このシラン化合物の分子内に存在する三級アミノ基がコ
ートキヤリヤに良好な正の帯電性および湿度安定性を付
与するのに有効である。That is, the present invention is characterized by comprising core particles and a coating layer of a tertiary amino group-containing silane compound thereon, wherein the tertiary amino group has a nitrogen atom bonded to a phenyl group and a lower alkyl group. Electrostatic image developing carrier particles The tertiary amino group present in the molecule of the silane compound is effective for imparting good positive charging property and humidity stability to the coat carrier.
本発明において使用する三級アミノ基含有シラン化合物
の具体例としては、N−メチル−N−フエニル−γ−ア
ミノプロピルトリメトキシシラン、N−エチル−N−フ
エニル−γ−アミノプロピルトリメトキシシラン、N−
イソプロピル−N−フエニル−γ−アミノプロピルトリ
メトキシシラン、N−t−ブチル−N−フエニル−γ−
アミノプロピルトリメトキシシラン、N−メチル−N−
フエニル−δ−アミノブチルトリメトキシシラン、N−
エチル−N−フエニル−δ−アミノブチルトリメトキシ
シラン、N−イソプロピル−N−フエニル−δ−アミノ
ブチルトリメトキシシラン、N−t−ブチル−N−フエ
ニル−δ−アミノブチルトリメトキシシラン、ビス−
(N−メチル−N−フエニル−γ−アミノプロピル)−
ジメトキシシラン、ビス−(N−メチル−N−フエニル
−δ−アミノブチル)−ジメトキシシラン等を挙げるこ
とができる。Specific examples of the tertiary amino group-containing silane compound used in the present invention include N-methyl-N-phenyl-γ-aminopropyltrimethoxysilane, N-ethyl-N-phenyl-γ-aminopropyltrimethoxysilane, N-
Isopropyl-N-phenyl-γ-aminopropyltrimethoxysilane, Nt-butyl-N-phenyl-γ-
Aminopropyltrimethoxysilane, N-methyl-N-
Phenyl-δ-aminobutyltrimethoxysilane, N-
Ethyl-N-phenyl-δ-aminobutyltrimethoxysilane, N-isopropyl-N-phenyl-δ-aminobutyltrimethoxysilane, Nt-butyl-N-phenyl-δ-aminobutyltrimethoxysilane, bis-
(N-methyl-N-phenyl-γ-aminopropyl)-
Examples thereof include dimethoxysilane and bis- (N-methyl-N-phenyl-δ-aminobutyl) -dimethoxysilane.
一方、本発明で使用するコア材料は四三酸化鉄、γ−三
二酸化鉄、MnZnフエライト、NiZnフエライト、Baフエラ
イト、鉄、ニツケル、コバルト、二酸化クロム、ガラス
ビーズ等の粉末であり、通常20〜500μm程度の粒径の
ものが使用される。On the other hand, the core material used in the present invention is powder of triiron tetraoxide, γ-ferric oxide, MnZn ferrite, NiZn ferrite, Ba ferrite, iron, nickel, cobalt, chromium dioxide, glass beads, etc. A particle size of about 500 μm is used.
本発明のキヤリヤ粒子は前述の如く、コア粒子を三級ア
ミノ基含有シラン化合物で表面処理することにより得ら
れ、被覆層が化学結合或いは吸着により該コア粒子上に
形成される。As described above, the carrier particles of the present invention are obtained by surface-treating core particles with a tertiary amino group-containing silane compound, and a coating layer is formed on the core particles by chemical bonding or adsorption.
本発明のキヤリヤ粒子を製造するためには、シラン化合
物の少なくとも1種を適当な溶媒、例えばアルコール、
ジオキサン中に溶解させ、得られる溶液中にコア粒子を
浸漬し、しかる後脱溶媒、乾燥、高温焼付けするか、或
いはコアを流動化床中で浮遊させ、前記シラン化合物含
有溶液を噴霧塗布し、乾燥し、次いで高温焼付けする等
の方法を利用することができる。To produce the carrier particles of the present invention, at least one silane compound is combined with a suitable solvent such as alcohol,
Dissolved in dioxane, soak the core particles in the resulting solution, then desolventization, drying, baking at high temperature, or floating the core in a fluidized bed, spray coating the silane compound-containing solution, A method such as drying and then baking at high temperature can be used.
上記キヤリヤの製造方法において、高温焼付けは必ずし
も必要とされないが、コアとシラン化合物との密着強度
を向上させるという観点から、約100〜200℃の高温焼付
け処理を行うことが望ましい。In the above method for producing a carrier, high temperature baking is not always necessary, but from the viewpoint of improving the adhesion strength between the core and the silane compound, it is desirable to perform high temperature baking treatment at about 100 to 200 ° C.
前記シラン化合物の被覆量は、通常コア材料100重量部
に対し0.001〜0.5重量部程度であることが好ましい。こ
のためには前記シラン化合物含有溶液中のシラン化合物
濃度は1〜4重量%であることが望ましい。しかしなが
ら、これより低濃度の溶液を使用することも可能であ
り、この場合には上記製造方法において浸漬、脱溶媒、
乾燥または噴霧塗布、乾燥といつた各工程を繰返して行
う。Usually, the coating amount of the silane compound is preferably about 0.001 to 0.5 parts by weight with respect to 100 parts by weight of the core material. For this purpose, the silane compound concentration in the silane compound-containing solution is preferably 1 to 4% by weight. However, it is also possible to use a solution with a lower concentration than this, in which case dipping, desolvation,
The steps of drying, spray coating and drying are repeated.
かくして得られる本発明のキヤリヤはトナーと混合し
て、静電潜像の現像剤として使用される。The carrier of the present invention thus obtained is mixed with toner and used as a developer for an electrostatic latent image.
トナーとしては、結着樹脂中に着色剤を分散した、通常
電子写真で使用されているいずれの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 toner in which a colorant is dispersed in a binder resin and which is generally used in electrophotography can be used and is not particularly limited.
発明の効果 本発明のキヤリヤを、通常使用されている電子写真用ト
ナーと混合した場合、該キヤリヤはトナーを負に帯電す
ることができ、しかも適当な飽和帯電量と著しく速い帯
電速度とを与えることができる。更に、被覆処理による
コア材料の電気抵抗変化が小さく、低抵抗被覆キヤリヤ
を得ることが可能となり、ソリツド再現性の優れた現像
剤を提供することができる。また、被覆に基きトナーに
よるキヤリヤの汚染が抑制されるので、キヤリヤの寿命
が長く、その結果寿命の長い現像剤を提供することがで
き、更に本発明のキヤリヤは溶液中への浸漬または溶液
の噴霧塗布等或いは必要に応じて加熱処理するといつた
簡単な工程で製造し得る等、数々の利点を有している。Effects of the Invention When the carrier of the present invention is mixed with a commonly used electrophotographic toner, the carrier can negatively charge the toner, and further, it gives an appropriate saturated charge amount and a remarkably high charging speed. be able to. Further, the change in electric resistance of the core material due to the coating treatment is small, and it becomes possible to obtain a low resistance coated carrier, and it is possible to provide a developer having excellent solid reproducibility. Further, since the carrier is suppressed from being contaminated by the toner based on the coating, the life of the carrier is long, and as a result, a developer having a long life can be provided. Furthermore, the carrier of the present invention is immersed in the solution or the solution of the solution. There are various advantages such as spray coating and the like, or heat treatment if necessary, which enables production in a simple process.
実施例 以下、本発明を実施例並びに比較例によつて更に具体的
に説明するが、本発明はこれら実施例によつて何等制限
されるものではない。EXAMPLES Hereinafter, the present invention will be described more specifically with reference to Examples and Comparative Examples, but the present invention is not limited to these Examples.
各例中において、「部」はすべて重量部を表わす。In each example, all "parts" represent parts by weight.
実施例 N−フエニル−N−メチル−δ−アミノブチルトリエト
キシシラン1部をメタノール50部に溶解した。この溶液
に平均粒度100μmの球状フエライト粒子100部を浸漬
し、90℃で1時間加熱することにより溶媒を除去した。
冷却後篩別により粗大粒子を除き、本発明の静電荷像現
像用キヤリヤ粒子を得た。Example 1 part of N-phenyl-N-methyl-δ-aminobutyltriethoxysilane was dissolved in 50 parts of methanol. 100 parts of spherical ferrite particles having an average particle size of 100 μm were immersed in this solution and heated at 90 ° C. for 1 hour to remove the solvent.
After cooling, coarse particles were removed by sieving to obtain carrier particles for developing an electrostatic charge image of the present invention.
比較例1 γ−アミノプロピルトリエトキシシランを用いて、前記
実施例と同様な操作に従つて、三級アミノ基ではなく一
級アミノ基を含有するシラン化合物で表面処理したキヤ
リヤ粒子を得た。Comparative Example 1 By using γ-aminopropyltriethoxysilane and following the same procedure as in the above-mentioned examples, carrier particles surface-treated with a silane compound containing a primary amino group instead of a tertiary amino group were obtained.
比較例2 実施例の球状フエライト粒子を無処理で用いた。Comparative Example 2 The spherical ferrite particles of Example were used without treatment.
上記三例のキヤリヤ粒子100部に対して、スチレン−n
−ブチルメタクリレート共重合体を結着樹脂として使用
した電子写真用トナー3部を混合して三種の現像剤を得
た。これら現像剤の帯電特性並びに画像特性を、常温常
湿条件下および高温高湿条件下で検討したところ、下表
のような結果を得た。For 100 parts of the carrier particles of the above three examples, styrene-n
Three kinds of developers were obtained by mixing 3 parts of an electrophotographic toner using a -butyl methacrylate copolymer as a binder resin. The charging characteristics and the image characteristics of these developers were examined under the conditions of normal temperature and normal humidity and high temperature and high humidity, and the results shown in the table below were obtained.
帯電特性並びに画像特性は夫々以下のような方法並びに
条件下で得た。 The charging characteristics and the image characteristics were obtained under the following methods and conditions, respectively.
前者はトナーとキヤリヤとを混合攪拌し、ブローオフ法
により測定した。後者については定着画像の画像濃度お
よびカブリ濃度を常法に従つて測定した。In the former, the toner and the carrier were mixed and stirred, and the measurement was performed by the blow-off method. For the latter, the image density and fog density of the fixed image were measured according to the usual method.
比較例3 二級アミノ基シラン化合物を用いて静電荷像現像用キャ
リア粒子を次のように作成した。Comparative Example 3 Carrier particles for developing an electrostatic charge image were prepared as follows using a secondary amino group silane compound.
γ−N−メチルアミノプロピルトリエトキシシラン1部
をメタノール50部に溶解した。この溶液に平均粒度100
μmの球状フェライト粒子100部を浸漬し、90℃で1時
間加熱することにより溶媒を除去した。冷却後、篩別に
より粗大粒子を除き、二級アミノ基を含有するキャリア
粒子を得た。このキャリアを使用して比較例2に記した
のと同様に現像剤を得て、この現像剤の帯電特性及び画
像特性を検討した。その結果、23℃、60%RHにおける帯
電量は13.5μC/gであって、画像性は良好であった。ま
た、30℃、90%RHにおける帯電量は8.0μC/gであって、
画像性は白地汚れ大であった。なお、帯電特性及び画像
特性は比較例2と同様の方法並びに条件下で得た。1 part of γ-N-methylaminopropyltriethoxysilane was dissolved in 50 parts of methanol. This solution has an average particle size of 100
The solvent was removed by immersing 100 parts of spherical ferrite particles of μm and heating at 90 ° C. for 1 hour. After cooling, coarse particles were removed by sieving to obtain carrier particles containing a secondary amino group. Using this carrier, a developer was obtained in the same manner as described in Comparative Example 2, and the charging property and the image property of this developer were examined. As a result, the charge amount at 23 ° C. and 60% RH was 13.5 μC / g, and the image quality was good. The charge amount at 30 ° C and 90% RH is 8.0 μC / g,
The image quality was large on a white background. The charging characteristics and the image characteristics were obtained under the same method and conditions as in Comparative Example 2.
───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 昭59−201064(JP,A) 特開 昭58−196550(JP,A) 特開 昭59−200259(JP,A) ─────────────────────────────────────────────────── ─── Continuation of front page (56) Reference JP-A-59-201064 (JP, A) JP-A-58-196550 (JP, A) JP-A-59-200259 (JP, A)
Claims (1)
ラン化合物の被覆層を含み、該三級アミノ基が窒素原子
にフェニル基かつ低級アルキル基が結合してなることを
特徴とする静電荷像現像用キャリヤ粒子。1. A core particle and a coating layer of a tertiary amino group-containing silane compound on the core particle, wherein the tertiary amino group has a nitrogen atom bonded to a phenyl group and a lower alkyl group. Carrier particles for electrostatic image development.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58098810A JPH0719079B2 (en) | 1983-06-03 | 1983-06-03 | Carrier particles for electrostatic image development |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58098810A JPH0719079B2 (en) | 1983-06-03 | 1983-06-03 | Carrier particles for electrostatic image development |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59223460A JPS59223460A (en) | 1984-12-15 |
| JPH0719079B2 true JPH0719079B2 (en) | 1995-03-06 |
Family
ID=14229682
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58098810A Expired - Lifetime JPH0719079B2 (en) | 1983-06-03 | 1983-06-03 | Carrier particles for electrostatic image development |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0719079B2 (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0934179A (en) * | 1995-07-19 | 1997-02-07 | Fuji Xerox Co Ltd | Electrophotographic carrier, electrifying member and production thereof |
| US6040101A (en) * | 1996-06-10 | 2000-03-21 | Nippon Shokubai Co., Ltd. | Carrier particles for use in electrostatic image development and electrostatic image developer |
| JPH10274944A (en) * | 1997-03-31 | 1998-10-13 | Nippon Shokubai Co Ltd | Substrate for liquid crystal display device and its production |
| EP0981570B1 (en) * | 1997-05-23 | 2002-10-16 | Bayer Ag | Organosilane oligomers |
-
1983
- 1983-06-03 JP JP58098810A patent/JPH0719079B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59223460A (en) | 1984-12-15 |
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