JPH03103865A - Bright magnetic toner - Google Patents

Bright magnetic toner

Info

Publication number
JPH03103865A
JPH03103865A JP1242766A JP24276689A JPH03103865A JP H03103865 A JPH03103865 A JP H03103865A JP 1242766 A JP1242766 A JP 1242766A JP 24276689 A JP24276689 A JP 24276689A JP H03103865 A JPH03103865 A JP H03103865A
Authority
JP
Japan
Prior art keywords
magnetic
thin film
metal oxide
plate
coloration
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
JP1242766A
Other languages
Japanese (ja)
Other versions
JP2734117B2 (en
Inventor
Yoshiko Ugajin
宇賀神 美子
Kenji Matsumoto
研二 松本
Hiroyuki Yasujima
安島 廣行
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.)
Toppan Inc
Original Assignee
Toppan Printing 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 Toppan Printing Co Ltd filed Critical Toppan Printing Co Ltd
Priority to JP1242766A priority Critical patent/JP2734117B2/en
Publication of JPH03103865A publication Critical patent/JPH03103865A/en
Application granted granted Critical
Publication of JP2734117B2 publication Critical patent/JP2734117B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PURPOSE:To obtain the bright magnetic toner suitable for coloration of the toner by applying the process for production of a pearl pigment. CONSTITUTION:A light coherent thin film consisting of a transparent metal oxide 11 having a high refractive index is formed on a planar magnetic particle 10. The color of the magnetic particle 10 is optically erased by the interference of the reflected light from the thin film surface of the metal oxide 11 and the reflected light from the boundary between the thin film of the metal oxide 11 and the magnetic particle 10, by which the magnetic particle is colored to the bright and beautiful color having brightness. Since the principle of the coloration is the interference effect of light, the coloration of many and diversified colors is enabled simply by changing the film thickness of the metal oxide 11. The bright magnetic toner suitable for the coloration is obtd. in this way.

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、磁気記録法などに用いられるトナ
ーに関し、特に、電子写真用一成分磁性トナー、および
磁気記録用トナーのカラー化に適する光沢磁性トナーに
関するものである。
[Detailed Description of the Invention] <Industrial Application Field> The present invention relates to toners used in electrophotography, magnetic recording, etc., and is particularly applicable to monocomponent magnetic toner for electrophotography and colorization of toner for magnetic recording. The present invention relates to suitable glossy magnetic toners.

〈従来の技術〉 従来より、例えば、磁気記録法においては磁性記録媒体
上に磁気的手法により得た磁気潜像を磁性トナーで現像
し、これを被転写物に転写させて定着することにより可
視画像を形成することが行なわれている。
<Prior art> Conventionally, for example, in the magnetic recording method, a magnetic latent image obtained by a magnetic method on a magnetic recording medium is developed with magnetic toner, and this is transferred and fixed onto an object to be transferred, thereby creating a visible image. Forming an image is performed.

ここで用いられる磁性トナーはF.,304あるいはバ
リウムーフェライト粉末等の磁性体粉末と樹脂を混練し
、粉砕したものが一般に知られている。
The magnetic toner used here is F. , 304 or barium-ferrite powder and resin are kneaded and pulverized.

一方、光沢を示す顔料として知られている真珠顔料は、
希薄な酸性チタン塩水溶液中に透明な雲母状基質を懸濁
させ、この懸濁液を加温し熱加水分解により基質表面永
和酸化チタン薄膜を形成させ、これを焼結して製造され
る。
On the other hand, pearl pigments are known as pigments that exhibit luster.
It is manufactured by suspending a transparent mica-like substrate in a dilute acidic titanium salt aqueous solution, heating this suspension, and forming a permanent titanium oxide thin film on the substrate surface by thermal hydrolysis, and sintering this.

さらに、特開昭51−7176号公報によれば、上記真
珠顔料の製造法を用い、不透明な雲母状酸化第二鉄表面
に酸化チタンの薄膜を形成させた酸化鉄顔料が開発され
ている。
Furthermore, according to JP-A-51-7176, an iron oxide pigment has been developed in which a thin film of titanium oxide is formed on an opaque mica-like ferric oxide surface using the above-mentioned pearl pigment production method.

〈発明が解決しようとする課題〉 従来の磁性トナーは磁性粉が黒色、あるいは黒褐色であ
るため、磁性粉と着色剤を単純に混合、あるいは磁性粉
を着色剤で単純に覆う場合、磁性粉の黒色、あるいは黒
褐色によりトナーの色に濁りが生し、鮮、明な色のトナ
ーが得られなかった。
<Problems to be Solved by the Invention> Since the magnetic powder in conventional magnetic toners is black or blackish-brown, when simply mixing the magnetic powder and a coloring agent or simply covering the magnetic powder with a coloring agent, it is difficult to The color of the toner became cloudy due to black or blackish brown, and a toner with a clear and bright color could not be obtained.

本発明は、磁気記録用トナー、あるいは電子写真用一或
分磁性トナーに関し、真珠顔料の製法を応用することに
より、カラー化に適する光沢磁性トナーを提供すること
を目的とする。
The present invention relates to toners for magnetic recording or semi-magnetic toners for electrophotography, and an object of the present invention is to provide a glossy magnetic toner suitable for coloring by applying a pearl pigment manufacturing method.

〈課題を解決するための手段〉 本発明は、上記の目的を達威するためになされたもので
あり、板状磁性粒子に高屈折率かつ透明性の金属酸化物
からなる光干渉性の薄膜を形成した光沢磁性トナーを提
供するものである。
<Means for Solving the Problems> The present invention has been made to achieve the above-mentioned objects, and includes an optical interference thin film made of a transparent metal oxide with a high refractive index on plate-shaped magnetic particles. The object of the present invention is to provide a glossy magnetic toner having the following properties.

板状磁性粒子は、磁性粒子単独あるいは数種の磁性粒子
の混合物であってもよく、板状非磁性粒子表面に磁性薄
膜を有する物質であってもよい。
The plate-shaped magnetic particles may be a single magnetic particle or a mixture of several types of magnetic particles, or may be a substance having a magnetic thin film on the surface of the plate-shaped nonmagnetic particles.

〈作用〉 上述の光沢磁性トナーは、板状磁性粒子上に高屈折率の
しかも透明な金属酸化物薄膜を設けているため、金属酸
化物薄膜表面からの反則光と、金属酸化物薄膜と磁性粒
子との界面からの反射光との干渉により磁性粒子の色が
光学的に消され鮮明な光沢のある優美な色に着色される
<Function> The above-mentioned glossy magnetic toner has a transparent metal oxide thin film with a high refractive index on the plate-shaped magnetic particles, so that the repulsive light from the surface of the metal oxide thin film and the magnetic property of the metal oxide thin film are prevented. The color of the magnetic particles is optically erased by interference with the reflected light from the interface with the particles, and the particles are colored in an elegant color with a clear luster.

また、着色の原理が光の干渉作用であるため、金属酸化
物の膜厚を変化させるだけで、多種多色の着色が可能と
なる。
In addition, since the principle of coloring is the interference effect of light, a wide variety of colors can be produced by simply changing the thickness of the metal oxide film.

さらに、着色顔料等を含んでいないため全ての色調のト
ナーがほとんど同一の物性を持っており、分散、混合な
どを均一にしかも容易に行うことができる。
Furthermore, since it does not contain color pigments, toners of all tones have almost the same physical properties, and can be uniformly and easily dispersed and mixed.

く発明の詳述〉 本発明を図面を用い、以下詳細に説明する。第1図は、
本発明の一実施例を示す断面図である。
DETAILED DESCRIPTION OF THE INVENTION The present invention will be described in detail below with reference to the drawings. Figure 1 shows
FIG. 1 is a sectional view showing an embodiment of the present invention.

図において、板状磁性粒子10としては、ニッケル、バ
リウムーフェライト、マグネタイト等、般に知られてい
る磁性体、あるいはそれらの合金、化合物が使用可能で
ある。この板状磁性粒子は、平均直径が2〜200μm
好ましくは5〜100μm1厚さが0.3〜5μm,好
ましくは0.5〜3μmがよい。形状は円板状、六角板
状、矩形3 4 板状、菱形板状、その他適宜の形状で平面性の良好なも
のであればよい。
In the figure, as the plate-shaped magnetic particles 10, generally known magnetic substances such as nickel, barium ferrite, magnetite, etc., or alloys and compounds thereof can be used. These plate-shaped magnetic particles have an average diameter of 2 to 200 μm.
The thickness is preferably 5 to 100 μm and 0.3 to 5 μm, preferably 0.5 to 3 μm. The shape may be a disc, a hexagonal plate, a rectangular plate, a rhombus plate, or any other appropriate shape as long as it has good planarity.

金属酸化物11としては高屈折率を示す二董化チタン、
酸化スズ、酸化ジルコニウムなどを用いることが可能で
ある。金属酸化物による薄膜形状方法としては、板状磁
性粒子10を有機金属化合物溶液に浸漬し引上げて乾燥
し、その後・焼威して有機金属化合物を分解することに
より金属酸化物よりなる薄膜を形或する方法、あるいは
金属塩の希薄酸性溶液中に板状磁性粒子を懸濁させ、金
属塩を加水分解してその表面に水和金属酸化物を析出さ
せ、焼威することにより金属化合物よりなる薄膜を形成
する方法があげられるが、これらの方法に限定されるも
のではない。ここで、最も一般的に用いられている酸化
チタン薄膜の形成方法をさらに詳しく説明する。
As the metal oxide 11, titanium oxide exhibits a high refractive index,
It is possible to use tin oxide, zirconium oxide, etc. As a method for forming a thin film using a metal oxide, the plate-shaped magnetic particles 10 are immersed in an organometallic compound solution, pulled up and dried, and then burned to decompose the organometallic compound to form a thin film made of a metal oxide. A method of suspending plate-shaped magnetic particles in a dilute acidic solution of a metal salt, hydrolyzing the metal salt to precipitate a hydrated metal oxide on its surface, and burning the metal compound. Examples include methods of forming a thin film, but the method is not limited to these methods. Here, the most commonly used method for forming a titanium oxide thin film will be explained in more detail.

温度約50〜100゜C及びpolo.5〜5.5を有
する被覆すべき物質の水懸濁液に、0.002〜3Nに
対当する遊離酸を含む0.001〜5モルのチタン塩水
溶液の第一の流れ及びそれと同時に1〜IONのアルカ
リ金属水溶液又は水酸化アンモニウム又はアンモニウム
ガスを添加することにより戒る。塩基の装入速度は、チ
タン塩溶液に含イJ゜される酸並びに反応中製逍される
酸を丁度中和することができるように維持する。チタン
塩の装入速度は、1分間被覆さるべき表面lm2当りチ
タン塩約0.01〜20X10−5モルのチタン塩の大
きさの範囲に維持する。
Temperature of about 50-100°C and polo. A first stream of an aqueous solution of a titanium salt of 0.001 to 5 molar containing free acid corresponding to 0.002 to 3N and at the same time an aqueous suspension of the material to be coated having a molecular weight of 5 to 5.5 This can be avoided by adding an aqueous alkali metal solution of ION or ammonium hydroxide or ammonium gas. The base charge rate is maintained just enough to neutralize the acid contained in the titanium salt solution as well as the acid produced during the reaction. The titanium salt charge rate is maintained in the range of about 0.01 to 20.times.10@-5 moles of titanium salt per square meter of surface to be coated per minute.

本発明によれば、加水分解は水溶液中で50〜100゜
C、特に70〜80゜Cで行なう。この加水分解におい
ては、それぞれ単位時間内に供給されるチタン塩の量、
又はそれから作ら・れる二酸化チタン水化物の量が被覆
さるべき表面と均衡するように、即ち表面によって実質
的に完全に吸収され遊離懸濁液における反応液中に残存
しないように注意しなければならない。
According to the invention, the hydrolysis is carried out in aqueous solution at 50-100°C, in particular 70-80°C. In this hydrolysis, the amount of titanium salt supplied within unit time,
Care must be taken that the amount of titanium dioxide hydrate produced therefrom is balanced with the surface to be coated, i.e. it is substantially completely absorbed by the surface and does not remain in the reaction solution in free suspension. .

加水分解は、被覆すべき物品又は物質が水中に挿入され
て懸濁液を形成するかもしくは物品の場合には上方から
懸吊させるようにして行うのが適当である。懸濁液を必
要な温度(約50〜100℃)にまで加熱した後、0.
001〜5モルの、希薄チタン塩水溶液を攪拌しながら
特に液体の水面下に供給する。濃度は0.2〜2モルの
範囲にあるのが望ましい。塩溶液は0.002〜3N、
特に0.2〜2.ONに対当する遊離酸を含有する。同
時に、希釈塩基水溶液又はアンモニアガスを懸濁液に供
給する。この塩基はチタン塩溶液に供給する。この塩基
はチタン塩溶液中に含まれる酸及び加水分解中連続的に
製造される酸の両方を中和するのに必要である。
Hydrolysis is suitably carried out in such a way that the article or substance to be coated is placed in water to form a suspension or, in the case of articles, suspended from above. After heating the suspension to the required temperature (approximately 50-100°C), 0.
A dilute titanium salt aqueous solution of 0.001 to 5 mol is fed under stirring, particularly below the surface of the liquid. Preferably, the concentration is in the range of 0.2 to 2 molar. Salt solution is 0.002-3N,
Especially 0.2~2. Contains the free acid corresponding to ON. At the same time, dilute aqueous base solution or ammonia gas is fed to the suspension. This base is fed to the titanium salt solution. This base is necessary to neutralize both the acid contained in the titanium salt solution and the acid produced continuously during hydrolysis.

塩基もチタン塩溶液も適当な計量装置によって供給する
のが有利である。適当な計量装置は例えば分配ポンプ及
びロタメーターを含む。
Advantageously, both the base and the titanium salt solution are supplied by suitable metering devices. Suitable metering devices include, for example, dispensing pumps and rotameters.

含水塩基としてはアルカリ金属水酸化物溶液が特に有用
であり、すぐれたものは水酸化ナトリウム又は水酸化カ
リウム又は水酸化アンモニウムである。0.025〜1
0、特に1〜loNの塩基溶液を使用するのが適当であ
る。単位時間当り供給される希簿塩括の量は狭い範囲内
で変えることができ、望ましからざる副産物を生しるこ
ともない。0.5〜5,0、特に1.5〜2.5の範囲
にあるPH値が良好な被覆の製造に特に適していること
が判明した。また、必要な場合にはこのpH値を維持す
るために緩衝剤を加えることもできる。このpH範囲に
常用のすべての緩衝系、例えば燐酸塩、酢酸塩、クエン
酸塩又はグリコール緩衝剤を使用することができる。
Particularly useful as hydrous bases are alkali metal hydroxide solutions, the preferred being sodium or potassium hydroxide or ammonium hydroxide. 0.025~1
It is suitable to use base solutions of 0, especially 1 to 1 loN. The amount of diluted salt fed per unit time can be varied within narrow limits without producing undesirable by-products. It has been found that pH values in the range from 0.5 to 5.0, in particular from 1.5 to 2.5, are particularly suitable for producing good coatings. Buffers can also be added to maintain this pH value if necessary. All buffer systems customary for this pH range can be used, such as phosphate, acetate, citrate or glycol buffers.

本発明によれば被覆すべき表面に単位時間当り単に十分
なチタン塩だけを供給し、全部の水酸化チタン又は二酸
化チタン水化物が、懸濁液中に可動性副産物を生しるこ
となく表面に沈積し得るようにすることができる。
According to the invention, only sufficient titanium salt is supplied per unit time to the surface to be coated, so that all the titanium hydroxide or titanium dioxide hydrate can be applied to the surface without forming mobile by-products in suspension. It can be made so that it can be deposited.

使用するチタン塩溶液の濃度もしくは供給速度を変える
ことによって他の可変要素に影響を与えること、及び両
可変要素が基質物質の表面を飽和するのに必要な二酸化
チタン又は含水二酸化チタンの割合に或る程度影響を与
えることは明白である。
By varying the concentration or feed rate of the titanium salt solution used, both variables may be influenced by the proportion of titanium dioxide or hydrous titanium dioxide required to saturate the surface of the substrate material. It is clear that this will have a significant impact.

1分間当たり使用されるヂタン塩の量は、被覆さるべき
表面lm2当りチタン塩0.01〜20XIO−’モル
程度である。
The amount of titanium salt used per minute is of the order of 0.01 to 20.times.IO-' mol of titanium salt per square meter of surface to be coated.

反応は、使用されるチタン塩溶液及び被覆さるべき物質
により、時間に関して広範に変えることができる。もち
ろん、使用量も重要な役割を果たす。例えば1〜4時間
後に特定の支持物上に被覆物を得ることができる(例え
ば硫酸バリウムの場合)が、他の支持物の場合には数日
までの相当長い時間が必要である。
The reaction can vary widely with respect to time, depending on the titanium salt solution used and the material to be coated. Of course, usage also plays an important role. For example, coatings can be obtained on certain supports after 1 to 4 hours (e.g. in the case of barium sulfate), whereas in the case of other supports considerably longer times, up to several days, are required.

本発明によって、含水二酸化チタン被覆が製造される。According to the present invention, a hydrous titanium dioxide coating is produced.

これらの被覆は単に空気中に放置するか又は強制乾燥に
よって完全に又は部分的に脱水される、二酸化チタンの
薄膜となる。
These coatings become thin films of titanium dioxide that are completely or partially dehydrated by simply being left in the air or by forced drying.

さらに、板状磁性粒子10としては、板状非磁性粒子2
0表面に磁性薄膜21を形成したものでもよい。板状非
磁性粒子としては、天然雲母、合或雲母が用いられる。
Furthermore, as the plate-shaped magnetic particles 10, plate-shaped non-magnetic particles 2
A magnetic thin film 21 may be formed on the zero surface. Natural mica and composite mica are used as the plate-like nonmagnetic particles.

磁性薄膜としては、ニッケル、バリウムーフェライト、
マグネタイト等一般に知られている磁性体、あるいはそ
れらの合金、化合物等が使用可能である。薄膜形或方法
としては、メッキ、蒸着、スバッタによる方法があげら
れるが、これらの方法に限定されるものではない。
As the magnetic thin film, nickel, barium-ferrite,
Generally known magnetic materials such as magnetite, alloys and compounds thereof, etc. can be used. Examples of the thin film method include plating, vapor deposition, and sputtering, but the method is not limited to these methods.

〈実施例〉 以下に本発明を実施例により具体的に説明する。<Example> The present invention will be specifically explained below using examples.

実施例−1 硫酸チタンの硫酸酸性溶液1000ml  (TiO,
換算25g)に平均径10μmの板状ニッケル粒子25
0gを加え、回転速度500rpmで攪拌しながら、9
5〜100゜Cで1時間加熱する。
Example-1 1000 ml of sulfuric acid acidic solution of titanium sulfate (TiO,
25 plate-shaped nickel particles with an average diameter of 10 μm (converted to 25 g)
Add 0 g and stir at a rotation speed of 500 rpm.
Heat at 5-100°C for 1 hour.

冷却後、水酸化ナトリウムにより中和し、硫酸イオンが
検出されなくなるまで水洗する。これをろ別乾燥し、光
沢のある青色の磁性トナーを得た。
After cooling, neutralize with sodium hydroxide and wash with water until sulfate ions are no longer detected. This was filtered and dried to obtain a glossy blue magnetic toner.

実施例−2 四塩化チタン40gを水lO00mlに溶解し、板状ニ
ッケル粒子250gを加え、実施例−1と同様の操作を
行い、光沢のある深緑色の磁性トナーを得た。
Example 2 40 g of titanium tetrachloride was dissolved in 100 ml of water, 250 g of plate-shaped nickel particles were added, and the same operation as in Example 1 was performed to obtain a glossy dark green magnetic toner.

実施例−3 メッキにより1μmのニッケル膜を形成した白色雲母(
平均径10μm)50gを硫酸チタンの硫酸酸性溶液1
 0 0 0 m l ( T i O z換算20g
)に加え、実施例−1と同様の操作を行い、光沢のある
紫色の磁性トナーを得た。
Example-3 White mica with a 1 μm nickel film formed by plating (
(average diameter 10 μm) 50g was added to a sulfuric acid acidic solution of titanium sulfate 1
0 0 0 ml (20g TiOz equivalent)
), and the same operations as in Example 1 were carried out to obtain a glossy purple magnetic toner.

く発明の効果〉 本発明は上述のとおりであり、板状磁性粒子上に高屈折
率かつ透明な金属酸化物薄膜が設けられているため、光
学的効果により磁性粒子の色が消され、鮮明な光沢のあ
る優美な色を有するトナーを得ることができる。
Effects of the Invention> The present invention is as described above, and since a high refractive index and transparent metal oxide thin film is provided on the plate-shaped magnetic particles, the color of the magnetic particles is erased by an optical effect, making it clear. It is possible to obtain a toner having a glossy and elegant color.

また、着色の原理が光の干渉作用であるため金属酸化物
の膜厚を変化させるだけで、多種多色に着色されたトナ
ーを得ることができる。
Furthermore, since the principle of coloring is light interference, toners colored in a wide variety of colors can be obtained by simply changing the thickness of the metal oxide film.

さらに、着色顔料等を含まないため、全ての色調のトナ
ーが殆んど同一の物性を示し、分散・混合などを均一・
容易に行える1・ナーとなり、電子写真法や磁気記録法
、マグネトグラフィー等の磁性画像形成技術に広く応用
できるものである。
Furthermore, since it does not contain coloring pigments, toners of all tones exhibit almost the same physical properties, ensuring uniform dispersion and mixing.
It is a 1-ner that can be easily performed and can be widely applied to magnetic image forming techniques such as electrophotography, magnetic recording, and magnetography.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は、本発明の光沢磁性トナーの実施例の断面図で
あり、第2図は、本発明に用いる板状磁性粒子の実施例
の断面図である。 l1 0・・・板状磁性粒子 1・・・金属酸化物 0・・・板状非磁性粒子 1・・・磁性粒子 特  許 凸 代 版 表 1 2
FIG. 1 is a cross-sectional view of an example of the glossy magnetic toner of the present invention, and FIG. 2 is a cross-sectional view of an example of plate-shaped magnetic particles used in the present invention. l1 0...Plate-shaped magnetic particles 1...Metal oxide 0...Plat-shaped non-magnetic particles 1...Magnetic particle patent Convex printing table 1 2

Claims (3)

【特許請求の範囲】[Claims] (1)板状磁性粒子に高屈折率かつ透明性の金属酸化物
からなる光干渉性の薄膜を形成したことを特徴とする光
沢磁性トナー。
(1) A glossy magnetic toner characterized in that a light interference thin film made of a transparent metal oxide with a high refractive index is formed on plate-shaped magnetic particles.
(2)板状磁性粒子が、磁性粒子単独、あるいは数種の
磁性粒子の混合物である請求項(1)記載の光沢磁性ト
ナー。
(2) The glossy magnetic toner according to claim 1, wherein the plate-shaped magnetic particles are a single magnetic particle or a mixture of several types of magnetic particles.
(3)板状磁性粒子が、板状非磁性粒子表面に磁性薄膜
を有するものである請求項(1)記載の光沢磁性トナー
(3) The glossy magnetic toner according to claim 1, wherein the plate-shaped magnetic particles have a magnetic thin film on the surface of the plate-shaped non-magnetic particles.
JP1242766A 1989-09-19 1989-09-19 Glossy magnetic toner Expired - Fee Related JP2734117B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1242766A JP2734117B2 (en) 1989-09-19 1989-09-19 Glossy magnetic toner

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1242766A JP2734117B2 (en) 1989-09-19 1989-09-19 Glossy magnetic toner

Publications (2)

Publication Number Publication Date
JPH03103865A true JPH03103865A (en) 1991-04-30
JP2734117B2 JP2734117B2 (en) 1998-03-30

Family

ID=17093960

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1242766A Expired - Fee Related JP2734117B2 (en) 1989-09-19 1989-09-19 Glossy magnetic toner

Country Status (1)

Country Link
JP (1) JP2734117B2 (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1997048024A1 (en) * 1996-06-10 1997-12-18 Nittetsu Mining Co., Ltd. Colored magnetic toner and process for preparing the same
EP0852977A1 (en) * 1995-03-14 1998-07-15 Nittetsu Mining Co., Ltd. Powder having multilayer film on its surface and process for preparing the same
EP1124165A1 (en) * 1995-04-07 2001-08-16 Indigo N.V. Toner particles
US6979523B1 (en) 1995-04-07 2005-12-27 Hewlett-Packard Development Company, Lp Toner material and method utilizing same
JP2010217817A (en) * 2009-03-19 2010-09-30 Konica Minolta Business Technologies Inc Image forming method
JP2010217816A (en) * 2009-03-19 2010-09-30 Konica Minolta Business Technologies Inc Image forming method
JP2010250046A (en) * 2009-04-15 2010-11-04 Konica Minolta Business Technologies Inc Image forming method

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0852977A1 (en) * 1995-03-14 1998-07-15 Nittetsu Mining Co., Ltd. Powder having multilayer film on its surface and process for preparing the same
EP0852977A4 (en) * 1995-03-14 1999-02-17 Nittetsu Mining Co Ltd Powder having multilayer film on its surface and process for preparing the same
US5985466A (en) * 1995-03-14 1999-11-16 Nittetsu Mining Co., Ltd. Powder having multilayered film on its surface and process for preparing the same
EP1124165A1 (en) * 1995-04-07 2001-08-16 Indigo N.V. Toner particles
US6979523B1 (en) 1995-04-07 2005-12-27 Hewlett-Packard Development Company, Lp Toner material and method utilizing same
WO1997048024A1 (en) * 1996-06-10 1997-12-18 Nittetsu Mining Co., Ltd. Colored magnetic toner and process for preparing the same
JP2010217817A (en) * 2009-03-19 2010-09-30 Konica Minolta Business Technologies Inc Image forming method
JP2010217816A (en) * 2009-03-19 2010-09-30 Konica Minolta Business Technologies Inc Image forming method
JP2010250046A (en) * 2009-04-15 2010-11-04 Konica Minolta Business Technologies Inc Image forming method

Also Published As

Publication number Publication date
JP2734117B2 (en) 1998-03-30

Similar Documents

Publication Publication Date Title
JP2864019B2 (en) Golden gloss pigment
KR960000646B1 (en) Process for preparing platelet-shaped coloured pigments
KR970001932B1 (en) Weather-resistant pearlescent pigments and process for producing the same
US5770310A (en) Composite fine particles of metal oxides and production thereof
CA2001933C (en) Nacreous pigments colored by adsorbed dyes
US4076551A (en) Carbon black-containing pigments and process for their preparation
KR870001881B1 (en) Transparent coloring pigment and manufacture
US4457784A (en) Green nacreous pigments having calcined Cr oxide and phosphate layer, their preparation, and use
KR910004813B1 (en) Nacreous pigments
JPH0465098B2 (en)
US4309480A (en) Iron blue nacreous pigments
JPS63130673A (en) Water-resistant pearlescent pigment and manufacture thereof
KR20030097856A (en) Effect pigments based on coated glass flakes
WO2006015530A1 (en) Pigment having angle dependence of the interference colors and its production process
KR19990068195A (en) Interference pigments having a blue mass tone
JPH04220467A (en) Mica pigment coated with metal oxide having light- and moisture vapor resistance and method of stabilization thereof
JP3184608B2 (en) Ultrafine barium sulphate coated flaky pigment and its production
JPH03103865A (en) Bright magnetic toner
CN111171602B (en) Preparation method of pearlescent pigment
US4047969A (en) Iron blue nacreous coated pigments
JP3336019B2 (en) Glazing-stable coloring pigment, its production method, its use and materials using it
JP2004346272A (en) White powdery material and method for producing the same
CN111995884A (en) Production process of color-changing pearlescent pigment
JPH0593148A (en) Pigment containing carbon black
CA2155680A1 (en) Process for making electroconductive powders

Legal Events

Date Code Title Description
LAPS Cancellation because of no payment of annual fees