JPS5857103B2 - dry developer powder - Google Patents

dry developer powder

Info

Publication number
JPS5857103B2
JPS5857103B2 JP51021495A JP2149576A JPS5857103B2 JP S5857103 B2 JPS5857103 B2 JP S5857103B2 JP 51021495 A JP51021495 A JP 51021495A JP 2149576 A JP2149576 A JP 2149576A JP S5857103 B2 JPS5857103 B2 JP S5857103B2
Authority
JP
Japan
Prior art keywords
parts
powder
developer powder
weight
particle size
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
Application number
JP51021495A
Other languages
Japanese (ja)
Other versions
JPS52104929A (en
Inventor
一雄 小林
彰 鈴木
久男 湯山
憲彦 稲葉
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.)
Ricoh Co Ltd
Original Assignee
Ricoh Co Ltd
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 Ricoh Co Ltd filed Critical Ricoh Co Ltd
Priority to JP51021495A priority Critical patent/JPS5857103B2/en
Priority to DE19772708061 priority patent/DE2708061C3/en
Publication of JPS52104929A publication Critical patent/JPS52104929A/en
Publication of JPS5857103B2 publication Critical patent/JPS5857103B2/en
Expired legal-status Critical Current

Links

Description

【発明の詳細な説明】 本発明は電子写真法、静電印刷法、静電記録法、磁気印
刷法などに用いられる圧力定着可能な乾式現像剤粉末に
関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a pressure fixable dry developer powder used in electrophotography, electrostatic printing, electrostatic recording, magnetic printing, and the like.

圧力定着法は、一対の圧力加重ローラーの間に現像剤粉
末画像を担う記録材料を通過させて定着するという手段
を採用するものであり、スイッチを入れてすぐに使用す
ることができ、環境汚染などの問題もな(、また高速で
連続操作した場合すべて完全に定着されるという点で有
利であるといわれている。
The pressure fixing method uses a means of passing the recording material carrying the developer powder image between a pair of pressure-loaded rollers and fixing it. It can be used immediately after turning on the switch, and does not pollute the environment. There are no problems such as this (and it is said to be advantageous in that everything is fixed completely when operated continuously at high speed.

しかし、この圧力定着法に使用される乾式現像剤粉末(
単に、現像剤粉末と称することもある)は、末だそれ自
体が、あるいは製造過程で種々のトラブルを生じ、充分
であるとはいえない。
However, the dry developer powder (
Developer powder (sometimes simply referred to as developer powder) is unsatisfactory because it causes various troubles either by itself or during the manufacturing process.

例えば、特開昭48−71648号公報、特開昭48−
75032号公報にみられるマイクロカプセルトナー粉
末は、その被覆樹脂がキャリアー粒子との摩擦帯電性向
および製造技術の両方の面から制約されている。
For example, JP-A-48-71648, JP-A-48-
The microcapsule toner powder disclosed in Japanese Patent No. 75032 is limited by both the triboelectric charging tendency of its coating resin with carrier particles and the manufacturing technology.

圧力定着用の乾式現像剤粉末のこうした欠点を解消する
ものとして、ワックス成分、熱可塑性樹脂、磁性粉およ
び着色剤から構成される現像剤粉末が提案されている。
To overcome these drawbacks of the dry developer powder for pressure fixing, a developer powder composed of a wax component, a thermoplastic resin, a magnetic powder, and a colorant has been proposed.

これによれば画像濃度、保存性なども満足しうるのであ
るが、その現像剤粉末の製造過程でワックス成分と熱可
塑性樹脂とが相分離し、容易な手段では現像剤粉末を得
ることができないといった嫌いがある。
According to this method, image density and storage stability can be satisfied, but the wax component and thermoplastic resin undergo phase separation during the manufacturing process of the developer powder, making it impossible to obtain the developer powder by easy means. There are some dislikes.

本発明の目的は、容易にかつ安価に製造でき、定着性に
すぐれ高い画像濃度が得られ、しかも高速度の複写又は
印刷装置に有用かつ安全に適用でき、良好な保存性を示
す乾式現像剤粉末を提供することにある。
An object of the present invention is to provide a dry developer that can be easily and inexpensively produced, has excellent fixing properties and provides high image density, can be usefully and safely applied to high-speed copying or printing equipment, and has good storage stability. The purpose is to provide powder.

すなわち本発明は、約35〜160’Cの融点をもつワ
ックス95〜70重量部と、平均粒径5μ以下の充填剤
5〜30重量部とを含み、かつ、粒径0.1〜2,5μ
の磁性体を現像剤粉末総重量に対し25〜75重量%の
割合で含有してなる乾式現像剤粉末である。
That is, the present invention comprises 95 to 70 parts by weight of a wax having a melting point of about 35 to 160'C, and 5 to 30 parts by weight of a filler having an average particle size of 5 microns or less, and having a particle size of 0.1 to 2. 5μ
This is a dry type developer powder containing 25 to 75% by weight of the magnetic material based on the total weight of the developer powder.

本発明の現像剤粉末には、着色剤を含有させることがで
きる。
The developer powder of the present invention can contain a colorant.

本発明に用いられるワックス成分としては、トナーに良
好な定着性を付与するために融点が約35〜160℃の
範囲のものが望ましく、公知のものすべてが使用できる
が、例示すれば、パラフィンロウ、結晶性ロウ、カルナ
ウバロウ、モンタンロウ、セレシンロウおよびサトウキ
ビロウの天然又は合成脂肪族ロウ、ステアリン酸パルミ
チン酸およびベヘン酸等の脂肪酸、ステアリン酸リチウ
ム、ステアリン酸アルミニウム、ステアリン酸バリウム
、パルミチン酸亜鉛等の脂肪酸金属塩、N(β−ヒドロ
キシエチル)−リシノールアミド、N−N’−エチレン
−ビス−リシノールアミド、N・N’−エチレン−ビス
−1・2−ヒドロキシステアリルアミド等のアミドヒド
ロキシロウ、エチレンホモポリマー、ジシクロへキシル
フタレート、ジフェニルフタレート、ヒドロキシステア
リン酸、エチレングリコールモノヒドキシステアレート
ナどをあげることができる。
The wax component used in the present invention preferably has a melting point in the range of about 35 to 160°C in order to impart good fixing properties to the toner, and all known wax components can be used, but examples include paraffin wax. , crystalline waxes, natural or synthetic aliphatic waxes such as carnauba wax, montan wax, ceresin wax and sugarcane wax, fatty acids such as palmitic stearate and behenic acid, fatty acids such as lithium stearate, aluminum stearate, barium stearate, zinc palmitate, etc. Metal salts, amide hydroxy waxes such as N(β-hydroxyethyl)-ricinolamide, N-N'-ethylene-bis-ricinolamide, N・N'-ethylene-bis-1,2-hydroxystearylamide, ethylene homo Examples include polymers, dicyclohexyl phthalate, diphenyl phthalate, hydroxystearic acid, and ethylene glycol monohydroxystearate.

これらワックス成分は2種以上同時に使用されてもよい
が、その配合量は充填剤に対して95〜70重量部が適
当である。
Two or more of these wax components may be used at the same time, but the appropriate amount is 95 to 70 parts by weight based on the filler.

また本発明に用いられる磁性体としては、例えば鉄粉、
四三酸化鉄粉、三二酸化鉄粉、クロム粉、二酸化クロム
粉、ニッケル粉などをあげることができる。
Further, as the magnetic material used in the present invention, for example, iron powder,
Examples include triiron tetroxide powder, iron sesquioxide powder, chromium powder, chromium dioxide powder, and nickel powder.

これら磁性体は2種以上同時に使用されてもよいが、そ
の配合量は現像剤粉末の総重量の25〜75重量%占め
るのが適当である。
Two or more of these magnetic substances may be used at the same time, but the appropriate amount thereof is 25 to 75% by weight of the total weight of the developer powder.

なお、これら磁性体の粒径は約0.10〜2.5μが適
当である。
In addition, the particle size of these magnetic substances is suitably about 0.10 to 2.5 microns.

いま、単に前記のワックス成分に磁性体を分散させてト
ナーをつくると、このトナーは凝集、ブリッジングなど
の現象を生じ、また定着されたトナー像は指でこすられ
ると簡単に取れてしまう。
If a toner is prepared by simply dispersing a magnetic material in the wax component described above, the toner will cause phenomena such as aggregation and bridging, and the fixed toner image will easily come off when rubbed with a finger.

こうした現象はワックス成分の硬度が、通常熱定着用ト
ナーに使用されている熱可塑性樹脂より低いために起る
ものである。
This phenomenon occurs because the hardness of the wax component is lower than that of the thermoplastic resin normally used in heat fixing toners.

しかし、ここに平均粒径5μ以下のMg又はCaの炭酸
塩、酸化物、水酸化物あるいは珪酸塩などの充填剤を添
加すれば、このような好ましくない現象を阻止すること
ができる。
However, by adding a filler such as Mg or Ca carbonate, oxide, hydroxide, or silicate having an average particle size of 5 μm or less, such undesirable phenomena can be prevented.

従って、本発明ではこれら充填剤をフックス成分に対し
て5〜30重量部重量部子いる。
Therefore, in the present invention, these fillers are present in an amount of 5 to 30 parts by weight based on the Fuchs component.

5重量部以下であるとその効果に乏しく、逆に30重量
部を超えるとり(られた現像剤粉末が定着しないように
なる。
If the amount is less than 5 parts by weight, the effect will be poor, and on the contrary, developer powder added in excess of 30 parts by weight will not be fixed.

これら充填剤としては炭酸カルシウム、炭酸マグネシウ
ム、水酸化マグネシウム、硫酸化バリウム、硫酸化カル
シウム、酸化マグネシウム、タルク、珪酸マグネシウム
、珪酸カルシウムなどがあげられるが、特に炭酸マグネ
シウム、炭酸カルシウムの使用が好ましい。
Examples of these fillers include calcium carbonate, magnesium carbonate, magnesium hydroxide, barium sulfate, calcium sulfate, magnesium oxide, talc, magnesium silicate, and calcium silicate, with magnesium carbonate and calcium carbonate being particularly preferred.

特にこれらが好ましいのは、本発明現像剤粉末の製造時
に、加熱溶融状態にあって他成分と混和され、さらに粉
砕される際にも何等分解、変質したりすることがな(、
得られた現像剤粉末の静電気特性を劣化させるものでな
いからであろうと考えられる。
These are particularly preferable because they are mixed with other components in a heated molten state during the production of the developer powder of the present invention, and do not undergo any decomposition or change in quality even when pulverized.
This is probably because it does not deteriorate the electrostatic properties of the obtained developer powder.

なお、含有される充填剤は製造される現像剤粉末の形状
を保ち、凝集を阻止するのに効果的である。
The filler contained is effective in maintaining the shape of the produced developer powder and preventing agglomeration.

上記のワックス成分と充填剤と磁性体とから構成される
現像剤粉末は、かなりの画像濃度を有するものであるが
、一層高濃度の現像剤粉末を希望する場合には、さらに
着色剤を加えればよい。
The developer powder composed of the wax component, filler, and magnetic material described above has a considerable image density, but if a developer powder with even higher density is desired, a coloring agent may be added. Bye.

着色材料としては、当該技術分野で用いられている従来
の顔料又は染料で、例えばカーボンブラック、アニリン
ブラック、チャンネルブラック、アセチレンブラック、
ランプブラックのような顔料、ビクトリアブルー、ファ
ーナルブルー、パーマネントフルートナー、ニグロシン
ベースなどの染料をあげることができる。
Coloring materials include conventional pigments or dyes used in the art, such as carbon black, aniline black, channel black, acetylene black,
Examples include pigments such as lamp black, dyes such as Victoria Blue, Furnal Blue, permanent flutners, and nigrosine bases.

これら着色剤の配合量は現像剤粉末の総重量の2〜10
重量%占めるのが適当である。
The blending amount of these colorants is 2 to 10% of the total weight of the developer powder.
It is appropriate to account for % by weight.

また、上記のごとき現像剤粉末の流動性を一層良好にす
るために、表面に微粒子状の無機顔料を付着させるのが
好ましい。
Further, in order to further improve the fluidity of the developer powder as described above, it is preferable to attach fine particulate inorganic pigments to the surface.

しかして、本発明の他の1つは、約35〜160℃の融
点をもつワックス95〜70重量部と、平均粒径5μ以
下の充填剤5〜30重量部とを含み、さらに粒径0.1
〜2.5μの磁性体を粉末総重量に対し25〜75重量
%の割合で含有した粉末の表面に、微粒子状の無機顔料
が付着されてなる粒径1〜30μの乾式現像剤粉末であ
る。
Accordingly, another aspect of the present invention includes 95 to 70 parts by weight of a wax having a melting point of about 35 to 160°C, and 5 to 30 parts by weight of a filler having an average particle size of 5 μm or less, and further contains 95 to 70 parts by weight of a wax having a melting point of about 35 to 160° C. .1
It is a dry developer powder with a particle size of 1 to 30μ, which is made by attaching a fine particulate inorganic pigment to the surface of a powder containing a magnetic material of ~2.5μ in a ratio of 25 to 75% by weight based on the total weight of the powder. .

ここで使用される無機顔料としては、例えば酸化チタン
、酸化ケイ素(シリカ)、酸化モリブデン、酸化亜鉛、
カーボンブラック、滑石粉末などがあげられ、その粒径
は0.1μ以下、好ましくは0.01μ以下である。
Inorganic pigments used here include, for example, titanium oxide, silicon oxide (silica), molybdenum oxide, zinc oxide,
Examples include carbon black and talcum powder, and the particle size thereof is 0.1 μ or less, preferably 0.01 μ or less.

本発明の現像剤粉末は上記のようなものであるが、これ
を実際につくるには、所定量のワックス成分、充填剤、
磁性体、さらに必要により着色材料を混合し、これを熱
ロールミルで150〜170°Cで溶融混練し、次いで
冷却し、ハンマーミルで粉砕し、さらにジェットミルで
微粉砕して粒径1〜30μのものを得ればよい。
The developer powder of the present invention is as described above, but in order to actually produce it, a predetermined amount of wax components, fillers,
The magnetic material and, if necessary, a coloring material are mixed, and this is melt-kneaded at 150 to 170°C with a hot roll mill, then cooled, crushed with a hammer mill, and further finely crushed with a jet mill to obtain a particle size of 1 to 30μ. All you have to do is get it.

また、このようにして得た粉末をそこで使用されたワッ
クス成分の融点より幾分低温の雰囲気で無機顔料粉末と
混合し、例えば風力分級機で余剰の無機顔料粉末を取除
けばよい。
Alternatively, the powder thus obtained may be mixed with an inorganic pigment powder in an atmosphere slightly lower than the melting point of the wax component used therein, and excess inorganic pigment powder may be removed using, for example, an air classifier.

この場合、顔料微粉末はワックス、充填剤を含む粉末の
表面に強固に付着している。
In this case, the pigment fine powder is firmly attached to the surface of the powder containing wax and filler.

なお、この顔料粉末の付着量は、それを除いた総重量1
00部に対して0.5〜2重量部が適当である。
In addition, the amount of adhered pigment powder is the total weight excluding it 1
A suitable amount is 0.5 to 2 parts by weight per 00 parts.

このようにして得られた本発明の現像剤粉末は所期の目
的を充分満足するものである。
The developer powder of the present invention thus obtained fully satisfies the intended purpose.

次に実施例および比較例を示す。Next, examples and comparative examples will be shown.

なお、部はすべて重量部である。Note that all parts are parts by weight.

比較例 ステアリン酸アルミニウム 100部酸化鉄
100部 カーボンブラック 20部よりなる
混合物を熱ロールミルで150〜170℃で、30分間
溶溶融金した。
Comparative example Aluminum stearate 100 parts Iron oxide
A mixture of 100 parts and 20 parts of carbon black was melted in a heated roll mill at 150-170°C for 30 minutes.

これを冷却後、ハンマーミルで粗粉砕し、さらにジェッ
トミルで微粉砕して平均粒径18μの比較現像剤粉末を
つくった。
After cooling, this was coarsely pulverized with a hammer mill and further finely pulverized with a jet mill to produce a comparative developer powder having an average particle size of 18 μm.

この現像剤粉末を、市販の酸化亜鉛タイプの圧力定着用
複写機で使用して複写を行なったところ、定着された画
像は指でこすると汚れるのが認められた。
When copying was carried out using this developer powder in a commercially available zinc oxide type pressure fixing copying machine, it was observed that the fixed image smeared when rubbed with a finger.

実施例 1 ステアリン酸アンモニウム 80部酸化鉄
100部 カーボンブラック 20部炭酸カル
シウム 20部よりなる化合物を、 比較例と同様な操作を行なっ て、平均粒径15/Jの現像剤粉末(本発明品1)とし
た。
Example 1 Ammonium stearate 80 parts iron oxide
A compound consisting of 100 parts carbon black, 20 parts, and 20 parts calcium carbonate was subjected to the same operation as in the comparative example to obtain a developer powder (product 1 of the present invention) having an average particle size of 15/J.

次いで、これをまた同様にして複写に供した。Next, this was also subjected to copying in the same manner.

一方、上記処方において炭酸カルシウム20部の代りに
酸化鉄20部を用いて(即ち酸化鉄が120部)現像剤
粉末−比較品A−を調製し、比較例と同様にして複写に
供した。
On the other hand, a developer powder - comparative product A- was prepared using 20 parts of iron oxide instead of 20 parts of calcium carbonate in the above formulation (ie, 120 parts of iron oxide), and was subjected to copying in the same manner as in the comparative example.

更に、上記処方において酸化鉄100部の代りに炭酸カ
ルシウム100部を用いて(即ち炭酸カルシウムが12
0部)現像剤粉末−比較品B−を調製した。
Furthermore, in the above formulation, 100 parts of calcium carbonate was used instead of 100 parts of iron oxide (i.e., 12 parts of calcium carbonate was used).
0 parts) Developer powder - Comparative product B- was prepared.

次いで、シート上にこの現像剤粉末(比較品B)を一様
に散布した後、コロナ放電によりプラスに帯電させ、こ
れに潜像を有する酸化亜鉛感光体を接触させて現像し、
圧力定着した。
Next, after uniformly scattering this developer powder (comparative product B) on the sheet, it was positively charged by corona discharge, and a zinc oxide photoreceptor having a latent image was brought into contact with it to develop it.
The pressure was established.

続いて、それぞれの現像画像(複写画像)上に白紙を載
せ、その上に先端にゴムが固定された押圧棒を3kg/
c4の圧力で押しつげ、白紙を押圧棒に対し位置を固定
させながら画ets持感光体(画像担持記録材料)を引
張り、白紙上に転移されたトナー(転移トナー)をマク
ベス拳度計で測定して定着性を調べたとこち、表−1の
ような結果が得られた。
Next, a blank sheet of paper was placed on top of each developed image (copy image), and a 3 kg press rod with a rubber tip fixed on top of the sheet was placed on top of each developed image (copy image).
Press down with a pressure of c4, pull the image-bearing photoreceptor (image-bearing recording material) while fixing the position of the white paper against the press rod, and measure the toner transferred onto the white paper (transferred toner) with a Macbeth fist meter. When the fixing properties were investigated, the results shown in Table 1 were obtained.

これより、本実施例の現像剤粉末の画像の定着性がすぐ
れていることが認められた。
From this, it was confirmed that the image fixing properties of the developer powder of this example were excellent.

実施例 ポリエチレンワックス 80部酸化鉄
100部 スピリットブラック 5部酸化マグネ
シウム 20部よりなる混合物を、比
較例と同様な操作を行なって、平均粒径18μの現像剤
粉末(本発明品2)とした。
Example polyethylene wax 80 parts iron oxide
A mixture consisting of 100 parts spirit black, 5 parts magnesium oxide, and 20 parts was subjected to the same operation as in the comparative example to obtain a developer powder (inventive product 2) having an average particle size of 18 μm.

次いで、これをまた同様にして複写に供した。Next, this was also subjected to copying in the same manner.

一方、上記処方において酸化マグネシウム20部の代り
に酸化鉄20部を用いて(即ち酸化鉄が120部)現像
剤粉末−比較品C−を調製し、比較例と同様にして複写
に供した。
On the other hand, developer powder - comparative product C- was prepared using 20 parts of iron oxide instead of 20 parts of magnesium oxide in the above formulation (ie, 120 parts of iron oxide), and was subjected to copying in the same manner as in the comparative example.

更に、上記処方において酸化鉄100部の代りに酸化マ
グネシウム100部を用いて(即ち酸化マグネシウムが
120部)現像剤粉末−比較品りを調製した。
Additionally, a comparative developer powder was prepared using 100 parts of magnesium oxide instead of 100 parts of iron oxide in the above formulation (i.e., 120 parts of magnesium oxide).

次いで、この比較品りを実施例1における比較品Bと同
様にして圧力定着に供した。
Next, this comparative product was subjected to pressure fixing in the same manner as comparative product B in Example 1.

続いて、それぞれの現像画像(複写画像)について実施
例1と同様な方法で定着性を調べたところ、表−2のよ
うな結果が得られた。
Subsequently, the fixability of each developed image (copied image) was examined in the same manner as in Example 1, and the results shown in Table 2 were obtained.

これより、本実施例の現像剤粉末の画像の定着性がすぐ
れていることが認められた。
From this, it was confirmed that the image fixing properties of the developer powder of this example were excellent.

実施例 3 実施例2で得た現像剤粉末100部に対しカーボンブラ
ック(粒径的0.02.z)1.5部を加えボールミル
中で約150℃の雰囲気で混合して、表面に無機顔料が
付着している別の現像剤粉末をつくった。
Example 3 1.5 parts of carbon black (particle size 0.02.z) was added to 100 parts of the developer powder obtained in Example 2 and mixed in a ball mill at about 150°C to coat the surface with inorganic Another developer powder was made that had pigment attached to it.

この現像剤粉末は凝集がまったくみられなかった。This developer powder showed no agglomeration at all.

また、これを使用した定着画像は実施例1と同様好結果
を示した。
Further, the fixed image obtained using the same showed good results as in Example 1.

Claims (1)

【特許請求の範囲】 1 約35〜160℃の融点をもつワックス95〜70
重量部と、平均粒径5μ以下の充填剤5〜30重量部と
を含み、がっ、粒径0.1〜2.5μの磁性体を現像剤
粉末総重量に対し25〜75重量%の割合で含有してな
る粒径1〜30μの乾式現像剤粉末。 2 約35〜160 ’Cの融点をもつワックス95〜
70重量部と、平均粒径5μ以下の充填剤5〜30重量
部とを含み、かつ、粒径o、1〜2.5μの磁性体を粉
末総重量に対し25〜75重量%の割合で含有したその
粉末の表面に、微粒子状の無機顔料が付着されてなる粒
径1〜30μの乾式現像剤粉末。
[Claims] 1 Wax 95-70 having a melting point of about 35-160°C
part by weight, and 5 to 30 parts by weight of filler with an average particle size of 5 μ or less, and 25 to 75 weight % of magnetic material with a particle size of 0.1 to 2.5 μ based on the total weight of the developer powder. A dry developer powder with a particle size of 1 to 30 μm. 2 Wax 95~ with a melting point of about 35~160'C
70 parts by weight, 5 to 30 parts by weight of filler with an average particle size of 5 μ or less, and a magnetic material with a particle size o of 1 to 2.5 μ in a proportion of 25 to 75 weight % based on the total weight of the powder. A dry developer powder having a particle size of 1 to 30 μm and having a finely divided inorganic pigment attached to the surface of the powder.
JP51021495A 1976-02-28 1976-02-28 dry developer powder Expired JPS5857103B2 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP51021495A JPS5857103B2 (en) 1976-02-28 1976-02-28 dry developer powder
DE19772708061 DE2708061C3 (en) 1976-02-28 1977-02-24 Toner for an electrostatographic dry developer

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP51021495A JPS5857103B2 (en) 1976-02-28 1976-02-28 dry developer powder

Publications (2)

Publication Number Publication Date
JPS52104929A JPS52104929A (en) 1977-09-02
JPS5857103B2 true JPS5857103B2 (en) 1983-12-19

Family

ID=12056541

Family Applications (1)

Application Number Title Priority Date Filing Date
JP51021495A Expired JPS5857103B2 (en) 1976-02-28 1976-02-28 dry developer powder

Country Status (1)

Country Link
JP (1) JPS5857103B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60120368A (en) * 1983-12-05 1985-06-27 Fuji Xerox Co Ltd Single-component nonmagnetic developer
DE102005046343A1 (en) 2005-09-28 2007-03-29 Saltigo Gmbh Preparation of 4-(aminomethyl)benzoic acid methylester, useful as pharmaceutical intermediates, comprises esterifying 4-aminomethylbenzoic acid with methanol in the presence of hydrochloric acid, solvent and separating organic phase

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2986521A (en) * 1958-03-28 1961-05-30 Rca Corp Reversal type electroscopic developer powder
US3639245A (en) * 1968-07-22 1972-02-01 Minnesota Mining & Mfg Developer power of thermoplastic special particles having conductive particles radially dispersed therein
JPS5140137A (en) * 1974-10-01 1976-04-03 Mita Industrial Co Ltd
JPS5188227A (en) * 1975-10-21 1976-08-02
JPS5199529A (en) * 1975-02-28 1976-09-02 Toyo Ink Mfg Co
JPS5240138A (en) * 1975-09-25 1977-03-28 Shigekazu Enoki Developing agent for electrostatic image

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2986521A (en) * 1958-03-28 1961-05-30 Rca Corp Reversal type electroscopic developer powder
US3639245A (en) * 1968-07-22 1972-02-01 Minnesota Mining & Mfg Developer power of thermoplastic special particles having conductive particles radially dispersed therein
JPS5140137A (en) * 1974-10-01 1976-04-03 Mita Industrial Co Ltd
JPS5199529A (en) * 1975-02-28 1976-09-02 Toyo Ink Mfg Co
JPS5240138A (en) * 1975-09-25 1977-03-28 Shigekazu Enoki Developing agent for electrostatic image
JPS5188227A (en) * 1975-10-21 1976-08-02

Also Published As

Publication number Publication date
JPS52104929A (en) 1977-09-02

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