JPH08202084A - Electrostatic charge image developer and carrier used for the developer - Google Patents

Electrostatic charge image developer and carrier used for the developer

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Publication number
JPH08202084A
JPH08202084A JP7013986A JP1398695A JPH08202084A JP H08202084 A JPH08202084 A JP H08202084A JP 7013986 A JP7013986 A JP 7013986A JP 1398695 A JP1398695 A JP 1398695A JP H08202084 A JPH08202084 A JP H08202084A
Authority
JP
Japan
Prior art keywords
carrier
magnetic particles
resin
developer
magnetic
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP7013986A
Other languages
Japanese (ja)
Other versions
JP3385496B2 (en
Inventor
Masafumi Uchida
雅文 内田
Kishiomi Tamura
希志臣 田村
Mayumi Hayashi
真由美 林
Yuji Marukawa
雄二 丸川
Kenji Yamane
健二 山根
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Konica Minolta Inc
Original Assignee
Konica Minolta Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Konica Minolta Inc filed Critical Konica Minolta Inc
Priority to JP01398695A priority Critical patent/JP3385496B2/en
Publication of JPH08202084A publication Critical patent/JPH08202084A/en
Priority to US08/971,096 priority patent/US6090517A/en
Application granted granted Critical
Publication of JP3385496B2 publication Critical patent/JP3385496B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

PURPOSE: To keep the quality of an image constant without generating toner spent or the stripping of a coated resin and changing chargeability even used over a long term by using a magnetic particle having an oxide of an element selected from among specific metals. CONSTITUTION: This carrier has a coated layer of a polyolefin resin formed on the magnetic body having Fe2 O3 and the oxide of the element selected from among Li, Be, Na, Mg, K, Ca, Rb by surface polymerization coating method. As a result, the stable image is obtained without varying the chargeability of the carrier since the specific gravity is decreased compared with the oxides of heavy metals such as copper or zinc to be conventionally used and then stress in a developing device is reduced. Since sintered primary particle diameter on the magnetic body surface is relatively uniformly and finely controlled, the polymerization of the resin on the surface proceeds uniformly and since the exposure of the magnetic body particle is prevented, the generation of the toner spent is prevented.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は静電荷像現像剤に用いて
有効なキャリアに関する。
FIELD OF THE INVENTION This invention relates to carriers useful in electrostatic image developers.

【0002】[0002]

【従来の技術】電子写真用等の静電荷像現像剤に用いる
キャリアとして、特開平2-187770号に記載される様な、
フェライト等の磁性体粒子の表面にポリオレフィンを重
合被覆せしめたものが提案されている。これはキャリア
へのトナースペントやキャリア被覆樹脂の摩耗がたいへ
ん改善された良好なキャリアではあるが、キャリア表面
の一部に磁性体粒子が露出している部分があったり、又
磁性体粒子表面の金属によっては重合が不安定になると
言う問題がある。このような磁性体粒子の露出部分には
特に高温高湿下でトナーがスペントしやすく、一方、重
合が不安定だとポリオレフィンと磁性体粒子の接着力が
弱く特に低温低湿下で膜剥がれが起こる。更に、フェラ
イトの比重は鉄粉のそれよりは小さいが、それでも重く
現像器内でのストレスで帯電性が変化する問題も未解決
であった。
2. Description of the Related Art As a carrier used for an electrostatic image developer for electrophotography, as described in JP-A-2-87770,
It has been proposed that the surface of magnetic particles such as ferrite is polymer-coated with polyolefin. This is a good carrier in which the toner spent on the carrier and the abrasion of the carrier coating resin have been greatly improved, but there is a part where the magnetic particles are exposed on the part of the carrier surface, and There is a problem that the polymerization becomes unstable depending on the metal. Toner is likely to be spent on the exposed portion of such magnetic particles particularly under high temperature and high humidity, while on the other hand, if the polymerization is unstable, the adhesive force between the polyolefin and the magnetic particles is weak and film peeling occurs especially under low temperature and low humidity. . Further, although the specific gravity of ferrite is smaller than that of iron powder, the problem that the chargeability is still heavy and the chargeability changes due to stress in the developing device has not been solved.

【0003】低比重化を目的として、特開平4-70853号
に記載の様に、磁性体を分散したバインダー型コアの表
面にポリオレフィンを重合したキャリアが提案されてい
る。確かにバインダー型キャリアは比重が2.0〜3.0と小
さく現像器内でのストレス低減には有効であるが、バイ
ンダー型コアの表面が比較的平滑で触媒を担持しにくい
傾向にあり、ポリオレフィンの重合被覆が不均質で、コ
アと被覆樹脂との接着力が弱いと言う問題がある。
For the purpose of lowering the specific gravity, a carrier in which a polyolefin is polymerized on the surface of a binder type core in which a magnetic material is dispersed has been proposed as described in JP-A-4-70853. Certainly, the binder type carrier has a small specific gravity of 2.0 to 3.0 and is effective in reducing stress in the developing unit, but the surface of the binder type core is relatively smooth and it is difficult to support the catalyst, and the polyolefin polymer coating Is inhomogeneous and the adhesive strength between the core and the coating resin is weak.

【0004】[0004]

【発明が解決しようとする課題】本発明は上記の事情に
よりなされたものであり、その目的は、長期にわたって
使用しても、トナースペントや被覆樹脂の剥がれが発生
せず、又、帯電性の変化がなく画像品位を一定に保つこ
とができる静電荷像現像剤に用いるキャリアを提供する
ことにある。
SUMMARY OF THE INVENTION The present invention has been made in view of the above circumstances, and an object thereof is to prevent the toner spent and the coating resin from peeling off even when used for a long period of time, and to prevent charging of the charging property. It is an object of the present invention to provide a carrier used for an electrostatic charge image developer capable of keeping the image quality constant without any change.

【0005】[0005]

【課題を解決するための手段】本発明の上記目的は、Fe
2O3及び、{Li、Be、Na、Mg、K、Ca、Rb}から選ばれ
る元素の酸化物を有する磁性体粒子に表面重合被覆法に
より形成されたポリオレフィン樹脂の被覆層を有するキ
ャリア、及び、該キャリアと、着色剤及び樹脂を含有す
るトナーとを含む静電荷像現像剤、によって達成され
る。
The above object of the present invention is to provide Fe
2 O 3 and a carrier having a coating layer of a polyolefin resin formed by a surface polymerization coating method on magnetic particles having an oxide of an element selected from {Li, Be, Na, Mg, K, Ca, Rb}, And an electrostatic image developer containing the carrier and a toner containing a colorant and a resin.

【0006】以下、本発明を詳述する。The present invention will be described in detail below.

【0007】本発明は、磁性体粒子に表面重合被覆法に
よるポリオレフィン樹脂の被覆層を有するキャリアの有
する技術課題を、Fe2O3及び、{Li、Be、Na、Mg、K、C
a、Rb}から選ばれる元素の酸化物を有する磁性体粒子
を採用して解決したものである。磁性体粒子が、{Li、
Be、Na、Mg、K、Ca、Rb}から選ばれる元素の酸化物を
有することによる効果として、 1) 従来含有されていた銅、亜鉛等の重金属の酸化物
に比べて比重を小さくでき、従って現像器中でのストレ
スを低減できるので、キャリアの帯電性の変化を招かず
に安定した画像を得ることができる 2) 磁性体表面の焼結一次粒子径(以下、焼結一次粒
子を「グレイン」と言う。)を比較的均一に且つ微細に
コントロールすることが可能なため、表面上でのポリオ
レフィン樹脂の重合が均一に進み易く、磁性体粒子の露
出を避けることができるため、トナースペントの発生を
防止できる 3) 磁性体粒子表面でのポリオレフィン樹脂の重合の
阻害が少ないため、磁性体粒子とポリオレフィン樹脂と
の界面での接着が強固で、どのような現像プロセスに用
いてもポリオレフィン被覆層が剥がれないことが挙げら
れる。
The present invention addresses the technical problems of a carrier having a coating layer of a polyolefin resin on a magnetic particle by a surface polymerization coating method, including Fe 2 O 3 and {Li, Be, Na, Mg, K, C.
The problem is solved by using magnetic particles having an oxide of an element selected from a, Rb}. The magnetic particles are {Li,
As an effect of having an oxide of an element selected from Be, Na, Mg, K, Ca, and Rb}, 1) the specific gravity can be made smaller than that of the conventionally contained heavy metal oxides such as copper and zinc. Therefore, since the stress in the developing device can be reduced, a stable image can be obtained without inducing a change in the chargeability of the carrier. 2) Sintered primary particle diameter on the surface of the magnetic material (hereinafter, the sintered primary particle is referred to as " Grain ") can be controlled relatively uniformly and finely, so that the polymerization of the polyolefin resin on the surface is likely to proceed uniformly and the exposure of the magnetic particles can be avoided. 3) Since there is little inhibition of the polymerization of the polyolefin resin on the surface of the magnetic particles, the adhesion at the interface between the magnetic particles and the polyolefin resin is strong, and it can be used for any development process. However, it is possible that the polyolefin coating layer does not peel off.

【0008】本発明の磁性体粒子が有する{Li、Be、N
a、Mg、K、Ca、Rb}から選ばれる元素の酸化物(以
下、「本発明の金属酸化物」とも言う。)は密度が2.0
g/cm2以下であり、Fe2O3と固溶体を形成することによ
って、適度な磁気特性及び低比重を得ることができる。
本発明の磁性体粒子の比重として好ましくは4.9g/cm3
以下、更には4.7g/cm3以下である。比重は、例えば気
相置換法による高精度自動体積計(例えば、エステック
社製VM-100等)を用いて測定することができる。
The magnetic particles of the present invention have {Li, Be, N
An oxide of an element selected from a, Mg, K, Ca, Rb} (hereinafter, also referred to as “metal oxide of the present invention”) has a density of 2.0.
It is g / cm 2 or less, and by forming a solid solution with Fe 2 O 3 , it is possible to obtain appropriate magnetic characteristics and low specific gravity.
The specific gravity of the magnetic particles of the present invention is preferably 4.9 g / cm 3.
Hereafter, it is 4.7 g / cm 3 or less. The specific gravity can be measured using, for example, a high-precision automatic volume meter (for example, VM-100 manufactured by STEC Co., Ltd.) by a gas phase substitution method.

【0009】本発明の金属酸化物は、原料時に必ずしも
酸化物である必要はなく、焼結後に酸化物となってもよ
い。原料としては、炭酸カルシウム、炭酸マグネシウ
ム、炭酸リチウム、硫酸リチウム等の酸素酸塩や、ハロ
ゲン化物、リチアキ石等の軽金属(リチウム)を主成分
とする鉱物等が挙げられる。
The metal oxide of the present invention does not necessarily have to be an oxide when it is used as a raw material, and may be an oxide after sintering. Examples of the raw material include oxyacid salts such as calcium carbonate, magnesium carbonate, lithium carbonate and lithium sulfate, and minerals containing a light metal (lithium) such as a halide and lithiacite as a main component.

【0010】本発明の金属酸化物のキャリア中での含有
率は、キャリア組成物全量に対して5〜50モル%程度、
好ましくは10〜45モル%である。5モル%以下では、低
比重を得ることができなかったり、均一で安定な樹脂の
重合ができなかったりすることがある。50モル%以上で
は、感光体上に形成した静電潜像を正確に現像し得る磁
気特性が得られないことがある。
The content of the metal oxide of the present invention in the carrier is about 5 to 50 mol% with respect to the total amount of the carrier composition,
It is preferably 10 to 45 mol%. If it is 5 mol% or less, low specific gravity may not be obtained, or uniform and stable resin polymerization may not be performed. If it is 50 mol% or more, the magnetic characteristics for accurately developing the electrostatic latent image formed on the photoreceptor may not be obtained.

【0011】本発明の金属酸化物の中でも、環境適性の
観点よりLi2O、Na2O、MgO、K2O、CaO、Rb2Oが好まし
く、又低比重を得易いこと、グレイン径の制御がし易い
ことによりLi2Oが好ましい。
Among the metal oxides of the present invention, Li 2 O, Na 2 O, MgO, K 2 O, CaO, and Rb 2 O are preferable from the viewpoint of environmental suitability, and it is easy to obtain a low specific gravity and Li 2 O is preferable because it is easy to control.

【0012】本発明においては、磁性体粒子のグレイン
の結晶化の促進及び均一な成長のために黄燐、赤燐、白
燐、黒燐、紫燐、金属燐、燐酸化物等の燐化合物を添加
することが好ましい。これにより、均一で微細なグレイ
ンを容易に得ることができ、キャリア強度も向上せし
め、現像器内での破壊に強いキャリアとすることができ
る。燐化合物の添加量としてはキャリア組成物全量に対
して0.05〜2重量%程度、更には0.1〜1重量%が好ま
しい。添加量が多すぎるとポリオレフィン樹脂の重合を
阻害する場合がある。
In the present invention, a phosphorus compound such as yellow phosphorus, red phosphorus, white phosphorus, black phosphorus, purple phosphorus, metal phosphorus, or phosphorus oxide is added to promote crystallization of grains of magnetic particles and to achieve uniform growth. Preferably. As a result, it is possible to easily obtain uniform and fine grains, improve the carrier strength, and make the carrier resistant to breakage in the developing device. The addition amount of the phosphorus compound is preferably about 0.05 to 2% by weight, more preferably 0.1 to 1% by weight, based on the total amount of the carrier composition. If the added amount is too large, it may hinder the polymerization of the polyolefin resin.

【0013】その他に、焼結促進剤(V2O5、As2O3、Bi2
O3、Sb2O3、PbO2、CuO、B2O3、SiO2、CaO、Cs、Nb等の
希土類化合物や、Li2CO3、CuSO4、CuCl2、CaCO3等の金
属化合物)、グレイン径制御剤、キャリアの電気抵抗及
び帯電量を制御する成分等を添加してもよいが、本発明
の効果を遺憾なく発揮せしめるために、これらの成分の
総含有量は3重量%以下とすることが好ましい。
In addition, a sintering accelerator (V 2 O 5 , As 2 O 3 , Bi 2
O 3 , Sb 2 O 3 , PbO 2 , CuO, B 2 O 3 , rare earth compounds such as SiO 2 , CaO, Cs, Nb, and metal compounds such as Li 2 CO 3 , CuSO 4 , CuCl 2 , CaCO 3 ) , A grain size controlling agent, a component for controlling the electric resistance and the charge amount of the carrier, etc. may be added, but in order to fully exert the effects of the present invention, the total content of these components is 3% by weight or less. It is preferable that

【0014】本発明の磁性体粒子は多数のグレインが焼
結された構造を持ち、磁性体粒子表面及び内部に多数の
微細な細孔を均一に形成することが可能なので、優れた
性能を付与することができる。即ち、磁性体粒子表面及
び内部に多数の微細な細孔を均一に形成すると、樹脂の
表面被覆を重合により行う際に用いる高活性な触媒を、
磁性体粒子表面だけでなく内部にも担持固定化せしめる
ことにより、磁性体粒子の内部から被覆樹脂を重合成長
させることができるので、磁性体粒子と被覆樹脂の接着
面積を大きくするのみならず、磁性体粒子内部の深い位
置まで密に被覆樹脂が存在する状態にでき、被覆樹脂の
剥がれを防止する。又、ポリオレフィンの重合は触媒が
担持された“グレインとグレインとの境界部分の細孔”
から開始するため、グレイン径が微細であることは磁性
体粒子の露出を無くすことに効果的である。ポリオレフ
ィンに比べて表面エネルギーの高い磁性体粒子の露出が
少ないと、その部分へのトナースペントが少なく、長期
に渡って安定した帯電性を維持することができ、高品質
なトナー画像を提供できる。
The magnetic particles of the present invention have a structure in which a large number of grains are sintered, and a large number of fine pores can be uniformly formed on the surface and inside of the magnetic particles, so that excellent performance is imparted. can do. That is, when a large number of fine pores are uniformly formed on the surface and inside of the magnetic particles, a highly active catalyst used when performing surface coating of the resin by polymerization,
By supporting and fixing not only the surface of the magnetic particles but also the inside, the coating resin can be polymerized and grown from the inside of the magnetic particles, so that not only the adhesion area between the magnetic particles and the coating resin is increased, The coating resin can be made to exist densely in a deep position inside the magnetic particles, and peeling of the coating resin can be prevented. In addition, the polymerization of polyolefin is carried by the catalyst, "pores at the boundary between grains".
The fine grain size is effective in eliminating the exposure of the magnetic particles. When the exposure of the magnetic particles having a higher surface energy than that of the polyolefin is less, the toner spent on that portion is less, stable chargeability can be maintained for a long time, and a high-quality toner image can be provided.

【0015】磁性体粒子の表面及び内部に適切な細孔を
形成するためには、磁性体粒子を構成するグレインの粒
径と焼結密度をコントロールすることが重要である。具
体的には、磁性体粒子を構成するグレインの平均粒径
が、磁性体粒子の平均粒径の1/100〜1/10の範囲に
あるものが好ましく、更には1/75〜1/20の範囲にあ
るものである。グレインの平均粒径が磁性体粒子の平均
粒径の1/100より小さいと、磁性体粒子の機械的強度
が不足して、現像器内で使用中にキャリアの破壊が生
じ、画像不良の原因となることがある。1/10を越える
と、磁性体粒子の表面及び内部に十分な細孔が存在せ
ず、被覆樹脂との接着力が低下する。尚、これらの平均
粒径は磁性体粒子を撮影したSEM写真を用いて計測す
ることができる。
In order to form appropriate pores on the surface and inside of the magnetic particles, it is important to control the particle size and the sintering density of the grains that make up the magnetic particles. Specifically, it is preferable that the average grain size of the grains constituting the magnetic grains is in the range of 1/100 to 1/10 of the average grain size of the magnetic grains, and further 1/75 to 1/20. It is in the range of. If the average particle size of the grains is smaller than 1/100 of the average particle size of the magnetic particles, the mechanical strength of the magnetic particles will be insufficient, and the carrier will be destroyed during use in the developing device, causing image defects. May be. If it exceeds 1/10, sufficient pores do not exist on the surface and inside of the magnetic particles, and the adhesive force with the coating resin decreases. Note that these average particle diameters can be measured using an SEM photograph of magnetic particles.

【0016】又、磁性体粒子の見かけ密度がそのグレイ
ンの焼結密度を反映するので、グレインの焼結密度は、
磁性体粒子の見かけ密度をパラメータとして評価でき
る。本発明においては、磁性体粒子の見かけ密度が1.60
〜2.60g/cm3程度、好ましくは1.80〜2.40gcm3のもの
を用いると、好ましい結果を得ることができる。見かけ
密度が1.60g/cm3より小さい場合では、グレイン間の
焼結強度即ち磁性体粒子の機械的強度が不足するため、
現像器内で使用中にキャリアの破壊が生じ、画像不良の
原因となることがある。2.60g/cm3を越えると、磁性
体粒子の内部に十分な細孔が存在せず、被覆樹脂との接
着力が低下する。尚、ここでの磁性体粒子の見かけ密度
は、JIS Z-2504に記載の方法で測定したものとする。
Further, since the apparent density of the magnetic particles reflects the sintered density of the grains, the sintered density of the grains is
The apparent density of magnetic particles can be evaluated as a parameter. In the present invention, the apparent density of magnetic particles is 1.60.
~2.60g / cm 3 or so, and preferably used as the 1.80~2.40Gcm 3, it is possible to obtain a preferable result. If the apparent density is less than 1.60 g / cm 3, the sintering strength between grains, that is, the mechanical strength of the magnetic particles will be insufficient.
The carrier may be destroyed during use in the developing device, which may cause a defective image. When it exceeds 2.60 g / cm 3 , sufficient pores do not exist inside the magnetic particles, and the adhesive force with the coating resin decreases. The apparent density of the magnetic particles here is measured by the method described in JIS Z-2504.

【0017】尚、磁性体粒子は焼結法、アトマイズ法等
の製造方法によって製造でき、必要に応じて2種以上の
微粉末を混合焼結する。
The magnetic particles can be manufactured by a manufacturing method such as a sintering method or an atomizing method, and if necessary, two or more kinds of fine powders are mixed and sintered.

【0018】得られた磁性体粒子表面に、表面重合被覆
法によりポリオレフィン樹脂を被覆して本発明のキャリ
アを得る。
The surface of the obtained magnetic particles is coated with a polyolefin resin by a surface polymerization coating method to obtain the carrier of the present invention.

【0019】本発明においてポリオレフィン樹脂は、オ
レフィンモノマーの重合物、具体的には、エチレン、プ
ロピレン、ブテン、ブタジエン等のオレフィンモノマー
の重合物を言う。
In the present invention, the polyolefin resin means a polymer of an olefin monomer, specifically, a polymer of an olefin monomer such as ethylene, propylene, butene and butadiene.

【0020】磁性体粒子表面に表面重合被覆法によりポ
リオレフィン樹脂を被覆する方法としては、例えば特開
昭60-106808号に記載の方法、具体的には、触媒を溶解
した溶液に予め本発明の磁性体粒子を分散含浸せしめ、
これにオレフィンモノマーを連続的に供給しつつ重合を
行う、等の方法が挙げられる。
The method of coating the surface of the magnetic particles with the polyolefin resin by the surface polymerization coating method is, for example, the method described in JP-A-60-106808, specifically, a method in which the solution of the catalyst of the present invention is previously prepared. Disperse and impregnate magnetic particles,
Examples thereof include a method in which polymerization is performed while continuously supplying an olefin monomer.

【0021】更に必要に応じて、キャリア被覆層中に荷
電制御剤、抵抗調整剤を添加することができる。これら
の添加剤は重合を阻害しないように、具体的には、反応
槽内に微粒子の状態で存在させておけば、重合時にキャ
リア被覆層中に取り込ませることができ、最終的には、
被覆層中に添加剤を分散させてキャリアを得ることがで
きる。
If necessary, a charge control agent and a resistance adjusting agent can be added to the carrier coating layer. These additives do not inhibit the polymerization, specifically, if they exist in the state of fine particles in the reaction tank, they can be incorporated into the carrier coating layer during the polymerization, and finally,
The carrier can be obtained by dispersing the additive in the coating layer.

【0022】荷電制御剤としては、シリカ、チタニア、
アルミナ、酸化錫、炭化ケイ素、硫酸バリウム、硫酸マ
グネシウム等を用いることができる。又、抵抗調整剤と
しては、例えば、カーボンブラック、アセチレンブラッ
ク、マグネタイト微粒子、フェライト微粒子、アルミニ
ウム,銅,ニッケル,鉄等の金属微粒子等を用いること
ができる。
As the charge control agent, silica, titania,
Alumina, tin oxide, silicon carbide, barium sulfate, magnesium sulfate and the like can be used. As the resistance adjusting agent, for example, carbon black, acetylene black, magnetite fine particles, ferrite fine particles, metal fine particles of aluminum, copper, nickel, iron or the like can be used.

【0023】磁性体粒子に対するポリオレフィン樹脂の
被覆量は、2.0〜12.0重量%程度、好ましくは3.0〜8.0
重量%である。2.0重量%より少ないと、磁性体粒子の
表面が露出しやすく、又、十分なストレス吸収の効果が
得られないことがある。12.0重量%を越えると、キャリ
アの流動性が低下するため、搬送不良による画像不良の
原因となることがある。
The coating amount of the polyolefin resin on the magnetic particles is about 2.0 to 12.0% by weight, preferably 3.0 to 8.0.
% By weight. If it is less than 2.0% by weight, the surface of the magnetic particles is likely to be exposed and a sufficient effect of absorbing stress may not be obtained. If it exceeds 12.0% by weight, the fluidity of the carrier is deteriorated, which may cause defective images due to poor conveyance.

【0024】本発明において、良好な現像性を得るため
には、1000エルステッドにおけるキャリアの磁化の強さ
(σlk)は35〜100emu/g程度、好ましくは45〜80emu
/gである。35emu/gより小さいと、現像スリーブへ
の磁気束縛力が小さいためキャリア付着が発生したり、
磁気ブラシが小さくなるため、高濃度で良好な画像が得
られないことがある。100emu/gより大きいと、磁気ブ
ラシが堅くなり、潜像を現像したトナーを掃き取る、所
謂スカベージョン現象を起こして、現像方向に対して垂
直な線を消失しやすくなることがある。
In the present invention, in order to obtain good developability, the strength of magnetization (σlk) of the carrier at 1000 oersted is about 35 to 100 emu / g, preferably 45 to 80 emu.
/ G. If it is less than 35 emu / g, the magnetic binding force to the developing sleeve is small and carrier adhesion may occur.
Since the magnetic brush becomes small, a good image may not be obtained at high density. If it is higher than 100 emu / g, the magnetic brush becomes hard and a so-called scavenge phenomenon occurs, in which the toner on which the latent image is developed is swept away, and a line perpendicular to the developing direction is likely to disappear.

【0025】キャリアの保磁力は100エルステッド以下
が好ましく、より好ましくは50エルステッド以下であ
る。100エルステッドを越えると、キャリア自身の凝集
が強くなり、トナーとの混合性が低下したり、固定磁石
を備えてなる現像スリーブ上ではキャリアが強く密着
し、現像剤の搬送性が大きく低下して画像ムラが発生す
ることがある。磁気特性の測定は、例えば市販の直流磁
化特性自動記録装置(横河電機社製;3257-35型、等)
により測定することができる。
The coercive force of the carrier is preferably 100 oersteds or less, more preferably 50 oersteds or less. If it exceeds 100 Oersteds, the cohesion of the carrier itself becomes strong, the mixing property with the toner deteriorates, and the carrier adheres strongly on the developing sleeve equipped with a fixed magnet, and the transportability of the developer decreases greatly. Image unevenness may occur. The magnetic characteristics can be measured by, for example, a commercially available DC magnetization characteristic automatic recording device (Yokogawa Electric Corp .; 3257-35 type, etc.)
Can be measured by

【0026】キャリア粒子の電気抵抗は1×107〜1×1
013Ωcmが好ましい。1×107Ωcmより小さいと、キャリ
ア粒子への感光体表面からの電荷の注入によるキャリア
付着が発生しやすく、1×1013Ωcmより大きい場合は、
高濃度の画像を得にくくなることがある。ここでは、電
気抵抗は体積固有抵抗のことを言い、次の様にして測定
したものとする。
The electric resistance of the carrier particles is 1 × 10 7 to 1 × 1.
0 13 Ωcm is preferred. If it is less than 1 × 10 7 Ωcm, carrier adhesion tends to occur due to injection of charges from the surface of the photoreceptor to carrier particles, and if it is more than 1 × 10 13 Ωcm,
It may be difficult to obtain a high-density image. Here, the electric resistance refers to volume resistivity, and is measured as follows.

【0027】キャリア1.0gを、断面積1.0cm2の絶縁性
円筒容器に充填し、100回タッピングを行って500gの荷
重下で試料高さを求めた後、DC100Vの電場を印加し
て電流値を測定する。(100〔V〕・断面積〔cm2〕)/
(電流値〔A〕・試料高さ〔cm〕)を体積固有抵抗値
〔Ωcm〕とする。
1.0 g of the carrier was filled in an insulating cylindrical container having a cross-sectional area of 1.0 cm 2 , tapped 100 times to obtain the sample height under a load of 500 g, and then an electric field of DC 100 V was applied to obtain a current value. To measure. (100 [V] / cross-sectional area [cm 2 ]) /
The volume resistivity (Ωcm) is defined as (current value [A] / sample height [cm]).

【0028】キャリア粒子の平均粒径は20〜300μmが好
ましく、より好ましくは30〜150μmである。20μmより
小さい場合は、感光体へのキャリア付着が発生しやす
く、300μmより大きい場合は、表面重合被覆時に反応槽
内で均一な撹拌ができず、被覆膜を均一に形成すること
が困難となる場合がある。ここでのキャリアの平均粒径
は、湿式分散機を備えてなるレーザー回折式粒度分布測
定装置(例えばシンパテック社製;HELOS)により
測定される体積基準の平均粒径とする。
The average particle size of the carrier particles is preferably 20 to 300 μm, more preferably 30 to 150 μm. If it is smaller than 20 μm, carrier adhesion to the photoconductor tends to occur, and if it is larger than 300 μm, uniform stirring cannot be performed in the reaction tank during surface polymerization coating, and it is difficult to form a coating film uniformly. May be. The average particle size of the carrier here is a volume-based average particle size measured by a laser diffraction type particle size distribution measuring device (for example, HELOS manufactured by Sympatech Co.) equipped with a wet dispersion machine.

【0029】本発明のキャリアと組み合わせられるトナ
ーには制限はなく、常法により作製された、結着樹脂、
着色剤を主成分とし、必要に応じて離型剤、荷電制御
剤、磁性体、流動化剤等を添加したものを使用できる。
There is no limitation on the toner to be combined with the carrier of the present invention, and a binder resin prepared by a conventional method,
A colorant may be used as a main component, and a release agent, a charge control agent, a magnetic material, a fluidizing agent and the like may be added if necessary.

【0030】[0030]

【実施例】以下、実施例を挙げて本発明を詳細に説明す
るが、本発明の態様はこれに限定されない。
The present invention will be described in detail below with reference to examples, but the embodiments of the present invention are not limited thereto.

【0031】実施例1 《磁性体粒子の作製》原料を秤量して表1に示す組成
(モル比)とした各組成物を、それぞれボールミルで混
合し、得られた混合物を仮焼、粉砕して、結着剤として
ポリビニルアルコールを加え、スプレードライヤーによ
り造粒した。その後焼成し磁性体粒子C1〜C9を得
た。尚、焼成条件は所望のグレイン径と比重が得られる
最適条件に設定した。又、磁性体粒子及びグレインの平
均粒径はSEM写真を用いて100個の磁性体粒子及びグ
レインについて計測して求めたものである。
Example 1 << Preparation of Magnetic Particles >> Raw materials were weighed and each composition having the composition (molar ratio) shown in Table 1 was mixed in a ball mill, and the obtained mixture was calcined and pulverized. Then, polyvinyl alcohol was added as a binder and granulated by a spray dryer. Then, it was fired to obtain magnetic particles C1 to C9. The firing conditions were set to the optimum conditions for obtaining the desired grain size and specific gravity. The average particle size of the magnetic particles and grains is obtained by measuring 100 magnetic particles and grains using an SEM photograph.

【0032】[0032]

【表1】 [Table 1]

【0033】《キャリアの作製》得られた磁性体粒子C
1の表面を、特開昭60-106808号に記載の表面重合被覆
法を参考にしてポリエチレン樹脂で被覆した。この際
に、カーボンブラック〔ライオンアクゾ社製;ケッチェ
ンブラックEC〕をポリエチレン樹脂に対して2.5重量
%添加分散したものを用いた。その後、目開き106μmの
篩によりスクリーニングして、通過して得られたキャリ
アをCC1とした。このキャリアの被覆量を熱天秤によ
り測定したところ、3.8重量%であった。
<< Preparation of Carrier >> Obtained Magnetic Particles C
The surface of No. 1 was coated with a polyethylene resin by referring to the surface polymerization coating method described in JP-A-60-106808. At this time, carbon black [Ketjen Black EC manufactured by Lion Akzo Co., Ltd.] was used by adding and dispersing 2.5% by weight with respect to the polyethylene resin. After that, screening was performed with a sieve having an opening of 106 μm, and the carrier obtained after passing through was designated as CC1. When the coating amount of this carrier was measured by a thermobalance, it was 3.8% by weight.

【0034】磁性体粒子、カーボンブラックの添加量、
ポリオレフィン樹脂とその被覆量を表2に示すように変
えた以外は同様の方法でキャリアCC2〜CC8及び比
較キャリア1を作製した。
The amount of magnetic particles and carbon black added,
Carriers CC2 to CC8 and comparative carrier 1 were produced by the same method except that the polyolefin resin and the coating amount thereof were changed as shown in Table 2.

【0035】[0035]

【表2】 [Table 2]

【0036】《正帯電性トナーの作製》スチレン/アク
リル共重合体樹脂100重量部に対し、離型剤として低分
子量ポリプロピレン〔三洋化成社製;ビスコール660
P〕4重量部、着色剤としてカーボンブラック〔キャボ
ット社製;ブラックパールL〕12重量部、4級アンモニ
ウム塩〔オリエント化学工業社製;P-51〕1重量部を
混合し、2軸混練機にて溶融混練を行った。
<< Preparation of Positively Chargeable Toner >> A low molecular weight polypropylene [manufactured by Sanyo Kasei Co., Ltd .; Viscol 660] is used as a release agent based on 100 parts by weight of a styrene / acrylic copolymer resin.
P] 4 parts by weight, as a colorant, 12 parts by weight of carbon black [manufactured by Cabot; Black Pearl L], 1 part by weight of quaternary ammonium salt [manufactured by Orient Chemical Co., Ltd .; P-51] are mixed to prepare a twin-screw kneader. Was melt-kneaded.

【0037】その後冷却、粗粉砕工程を経て、微粉砕、
風力分級を行い、平均粒径が7.5μmの着色粒子を得た。
更に、流動化剤として正帯電性疎水性シリカ微粒子〔ワ
ッカーケミカル社製;HDK-H2050E〕を着色粒子に
対して1.0重量部外添混合し、ここで用いるトナーとし
た。
Then, after cooling and coarse crushing steps, fine crushing,
Wind classification was performed to obtain colored particles having an average particle size of 7.5 μm.
Further, 1.0 part by weight of positively charged hydrophobic silica fine particles [HDK-H2050E manufactured by Wacker Chemical Co.] as a fluidizing agent was externally mixed with the colored particles to obtain a toner used here.

【0038】《正帯電性現像剤の調製》キャリア500g
とトナー26gをV型混合器に投入し、20分間混合して2
成分現像剤を調製する作業を、キャリアCC1〜CC5
及び比較キャリア1のそれぞれについて行い、現像剤1
〜8及び比較現像剤1を得た。
<< Preparation of Positively Chargeable Developer >> 500 g of carrier
26g of toner and toner are put into a V-type mixer and mixed for 20 minutes.
Carrier CC1 to CC5 is used to prepare the component developer.
And Comparative Carrier 1 for each developer 1
~ 8 and Comparative Developer 1 were obtained.

【0039】《性能評価》各現像剤について、その526
gを市販の複写機〔コニカ(株)製;U-Bix4155〕に搭載
し、20℃,50%RHの条件下で1万枚、続いて10℃、20%
RHで4万枚、更に33℃、80%RHで1万枚の計10万枚複写
して実写評価を行った。評価項目は以下の通り。
<< Performance Evaluation >> For each developer, 526
g in a commercially available copier [Konica Corporation; U-Bix4155], 10,000 sheets under conditions of 20 ° C and 50% RH, then 10 ° C and 20%
A total of 100,000 copies of 40,000 sheets at RH and 10,000 sheets at 33 ° C and 80% RH were copied and evaluated for actual shooting. The evaluation items are as follows.

【0040】(画像濃度)原稿濃度1.30のベタ画像を複
写し、複写1枚目と最終複写のものの出力画像の白紙に
対する相対反射濃度をマクベス濃度計(マクベス社製)
を用いて測定した。画像濃度1.30以上を良好であると判
断した。
(Image Density) A solid image having an original density of 1.30 is copied, and the relative reflection densities of the output images of the first copy and the final copy with respect to a blank sheet are measured by a Macbeth densitometer (manufactured by Macbeth Co.).
It measured using. An image density of 1.30 or higher was judged to be good.

【0041】(カブリ濃度)複写終了後、白紙原稿を複
写し、その出力画像の白紙に対する相対反射濃度をマク
ベス濃度計(マクベス社製)を用いて測定した。画像濃
度0.005以下は良好であると判断した。
(Fog Density) After completion of copying, a blank original was copied and the relative reflection density of the output image with respect to the blank was measured using a Macbeth densitometer (manufactured by Macbeth). An image density of 0.005 or less was judged to be good.

【0042】(現像剤の帯電量)帯電量の測定は、20
℃、50%RHにおいて、ブローオフ粉体帯電量測定装置T
B-200(東芝ケミカル社製)により測定した。尚、測定
は複写1枚目と終了時の2度行い、両者の帯電量の差が
少ない程良好であると判断した。
(Amount of charge of developer) The amount of charge is 20
Blow-off powder charge amount measuring device T at ℃, 50% RH
It was measured with B-200 (manufactured by Toshiba Chemical Co.). The measurement was performed twice on the first copy and at the end, and it was judged that the smaller the difference in charge amount between the two, the better.

【0043】(ポリオレフィン樹脂被覆層の剥離)複写
終了後、現像器内からキャリアをサンプリングし、SE
Mにより任意の100個のキャリアについて表面観察を行
った。キャリア表面に樹脂被覆層の破損や剥離が観察さ
れたキャリア粒子の個数による評価を行い、異常の見ら
れるキャリア粒子の個数が100個当たり5個以下のもの
は良好と判断した。
(Peeling off the polyolefin resin coating layer) After the copying is completed, the carrier is sampled from inside the developing device and SE
Surface observation was performed on 100 arbitrary carriers by M. The number of carrier particles in which breakage or peeling of the resin coating layer was observed on the surface of the carrier was evaluated, and when the number of abnormal carrier particles was 5 or less per 100, it was judged as good.

【0044】(トナースペント)現像剤から界面活性剤
を用いてキャリアのみを分離し、分離したキャリア3.0
gを100mlのメチルエチルケトン中に浸してスペント物
を溶かし、その溶液の500nmにおける透過率を分光光度
計(330型日立自記分光光度計)により測定し、その値
をスペント量(キャリア汚染度)とした。スペント物が
ない場合は100%であり、スペントの増加により値は小
さくなる。
(Toner Spent) The carrier is separated from the developer by using a surfactant, and the separated carrier 3.0
The spent substance was dissolved by immersing g in 100 ml of methyl ethyl ketone, and the transmittance of the solution at 500 nm was measured by a spectrophotometer (330 type Hitachi self-recording spectrophotometer), and the value was taken as the amount of spent (carrier contamination degree). . The value is 100% when there are no spent objects, and the value decreases as the amount of spent increases.

【0045】以上の結果を表3に示す。Table 3 shows the above results.

【0046】[0046]

【表3】 [Table 3]

【0047】[0047]

【発明の効果】実施例にて実証した様に、本発明のキャ
リアでは、実写終了後もキャリア表面のポリオレフィン
被覆層の剥がれやトナースペントが起こらず、高品質な
出力画像を終始得ることができる。
As demonstrated in the examples, with the carrier of the present invention, the polyolefin coating layer on the surface of the carrier is not peeled off or the toner spent is not generated even after the actual copying, and a high quality output image can be obtained all the time. .

【0048】尚、本発明のキャリアはこのように重金属
の含有率が小さいので、使用後廃棄しても、環境を著し
く汚染することが無い。
Since the carrier of the present invention has such a low content of heavy metals, it does not significantly pollute the environment even if it is discarded after use.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 G03G 9/10 321 (72)発明者 丸川 雄二 東京都八王子市石川町2970番地コニカ株式 会社内 (72)発明者 山根 健二 東京都八王子市石川町2970番地コニカ株式 会社内─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification number Internal reference number FI Technical indication location G03G 9/10 321 (72) Inventor Yuji Marukawa 2970 Ishikawacho, Hachioji, Tokyo Konica Stock Company ( 72) Inventor Kenji Yamane 2970 Ishikawa-cho, Hachioji City, Tokyo Konica Stock Company

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 Fe2O3及び、{Li、Be、Na、Mg、K、C
a、Rb}から選ばれる元素の酸化物を有する磁性体粒子
に表面重合被覆法により形成されたポリオレフィン樹脂
の被覆層を有することを特徴とするキャリア。
1. Fe 2 O 3 and {Li, Be, Na, Mg, K, C
A carrier characterized in that it has a coating layer of a polyolefin resin formed by a surface polymerization coating method on magnetic particles having an oxide of an element selected from a, Rb}.
【請求項2】 請求項1に記載のキャリアと、着色剤及
び樹脂を含有するトナーとを含むことを特徴とする静電
荷像現像剤。
2. An electrostatic charge image developer comprising the carrier according to claim 1 and a toner containing a colorant and a resin.
JP01398695A 1995-01-19 1995-01-31 Electrostatic image developer and carrier used therefor Expired - Fee Related JP3385496B2 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP01398695A JP3385496B2 (en) 1995-01-31 1995-01-31 Electrostatic image developer and carrier used therefor
US08/971,096 US6090517A (en) 1995-01-19 1997-11-14 Two component type developer for electrostatic latent image

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP01398695A JP3385496B2 (en) 1995-01-31 1995-01-31 Electrostatic image developer and carrier used therefor

Publications (2)

Publication Number Publication Date
JPH08202084A true JPH08202084A (en) 1996-08-09
JP3385496B2 JP3385496B2 (en) 2003-03-10

Family

ID=11848557

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005062132A3 (en) * 2003-12-22 2005-08-11 Powdertech Co Ltd Resin-coated carrier for electrophotographic developing agent, process for producing the same and electrophotographic developing agent utilizing the resin-coated carrier
JP2006053201A (en) * 2004-08-10 2006-02-23 Ricoh Co Ltd Carrier for electrophotography, developer and image forming apparatus
US7183033B2 (en) 2003-02-07 2007-02-27 Powdertech Co., Ltd. Carrier core material, coated carrier, two-component developing agent for electrophotography, and image forming method
US7553597B2 (en) 2003-02-07 2009-06-30 Powdertech Co., Ltd. Carrier core material, coated carrier, and two-component developing agent for electrophotography

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7183033B2 (en) 2003-02-07 2007-02-27 Powdertech Co., Ltd. Carrier core material, coated carrier, two-component developing agent for electrophotography, and image forming method
US7553597B2 (en) 2003-02-07 2009-06-30 Powdertech Co., Ltd. Carrier core material, coated carrier, and two-component developing agent for electrophotography
WO2005062132A3 (en) * 2003-12-22 2005-08-11 Powdertech Co Ltd Resin-coated carrier for electrophotographic developing agent, process for producing the same and electrophotographic developing agent utilizing the resin-coated carrier
US8092971B2 (en) 2003-12-22 2012-01-10 Powdertech Co., Ltd. Resin-coated carrier for electrophotographic developer and process for producing the same, and electrophotographic developer comprising the resin-coated carrier
JP2006053201A (en) * 2004-08-10 2006-02-23 Ricoh Co Ltd Carrier for electrophotography, developer and image forming apparatus

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