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JPS6040020B2 - Positively charged cyan toner for electrophotography - Google Patents

Positively charged cyan toner for electrophotography

Info

Publication number
JPS6040020B2
JPS6040020B2 JP52151823A JP15182377A JPS6040020B2 JP S6040020 B2 JPS6040020 B2 JP S6040020B2 JP 52151823 A JP52151823 A JP 52151823A JP 15182377 A JP15182377 A JP 15182377A JP S6040020 B2 JPS6040020 B2 JP S6040020B2
Authority
JP
Japan
Prior art keywords
electrophotography
toner
positively charged
cyan toner
manufactured
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
JP52151823A
Other languages
Japanese (ja)
Other versions
JPS5484732A (en
Inventor
一男 野島
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 JP52151823A priority Critical patent/JPS6040020B2/en
Publication of JPS5484732A publication Critical patent/JPS5484732A/en
Publication of JPS6040020B2 publication Critical patent/JPS6040020B2/en
Expired legal-status Critical Current

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  • Developing Agents For Electrophotography (AREA)

Description

【発明の詳細な説明】 本発明は、電子写真法等において、負の静電潜像を現像
するための電子写真用正荷電トナーに関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a positively charged toner for electrophotography for developing a negative electrostatic latent image in electrophotography and the like.

電子写真法には種々の方法があるが、一般には光導電性
絶縁体層上に一様な静電荷を与え、その絶縁体層に光像
照射することによって静電潜像を形成せしめ、これを鉄
粉、ガラス球等のキャリアとの摩擦によって帯電させた
樹脂を主成分とする乾式トナーで可視化し、ついで紙な
どにその粉像を転写したのち、加熱、加圧あるいは溶剤
蒸気などによって定着するものである。
There are various methods for electrophotography, but in general, a uniform electrostatic charge is applied to a photoconductive insulating layer, and an electrostatic latent image is formed by irradiating the insulating layer with a light image. The powder image is visualized using a dry toner whose main component is a resin that is charged by friction with a carrier such as iron powder or glass bulbs, and then the powder image is transferred to paper, etc., and then fixed by heat, pressure, or solvent vapor. It is something to do.

そしてカラー電子写真法においては原稿を色分解フィル
夕(ブルー、グリーン、レッド)を用いて露光し、前記
の各工程をイエロー、マゼンタ、シアンの各カラートナ
ーを用いて複数回線返し、カラー画像を得るものである
In color electrophotography, the original is exposed using color separation filters (blue, green, and red), and each of the above steps is repeated multiple times using yellow, magenta, and cyan color toners to produce a color image. It's something you get.

従来よりキャリアとの摩擦により正に帯電するシアント
ナーに使用されてきた樹脂として、ポリスチレン系樹脂
、ヱポキシ系樹脂、フェノール系樹脂等があるが、これ
らの樹脂は単独ではキャリア鉄粉との摩擦で弱い負帯電
を示すので、正荷蟹性トナーとして用いるためには、正
荷電制御作用の強い樹脂または着色剤を使用することが
一般に行なわれてきた。
Conventionally, there are polystyrene resins, epoxy resins, phenolic resins, etc. as resins used in cyan toners that are positively charged due to friction with the carrier. Since it exhibits a weak negative charge, in order to use it as a positively charged toner, it has generally been done to use a resin or colorant with a strong positive charge control effect.

しかし、その数は非常に少なく、またあってもそれぞれ
固有の欠点を有している。
However, there are very few of them, and even if there are, each has its own drawbacks.

例えば、正極性を与える基として第一級アミノ基(−N
H2)、第二級ァミノ基(一NHR)、第三級アミノ基
(NR、R2)、ピリジニウム基等を導入した樹脂は、
熱定着時にその官能基による不快臭を発生したり、高温
の環境では荷電制御作用が低下したりするなどの欠点が
あった。
For example, a primary amino group (-N
H2), a secondary amino group (1NHR), a tertiary amino group (NR, R2), a pyridinium group, etc. are introduced into the resin.
There are drawbacks such as generation of an unpleasant odor due to the functional group during heat fixing and a decrease in charge control effect in a high-temperature environment.

また、着色剤では例えばフタロシアニンブルー系顔料(
C・174160 74100)などを多量に用いない
とその効果が出ないなどの欠点があった。したがって、
いずれにしても明瞭な正極性のトナーを作るために選択
できる樹脂および着色剤は大きく制約されることになり
、しかも乾式シアントナーとして必要な諸特性すなわち
、色調、透明性、耐光性、定着性、保存性、流動性等を
考慮すると、使用できる樹脂および着色剤はほとんどな
かつた。
In addition, colorants such as phthalocyanine blue pigments (
C. 174160 74100), etc., had the disadvantage that the effect could not be obtained unless a large amount was used. therefore,
In any case, the resins and colorants that can be selected to create a toner with clear positive polarity are severely limited, and the characteristics necessary for a dry cyan toner, such as color tone, transparency, light fastness, and fixing properties, are severely limited. Considering storage stability, fluidity, etc., there are almost no resins or colorants that can be used.

本発明は荷電制御効果の強い化合物を用い、少量でも十
分に正極性を示すとともに、使用する樹脂の種類に制限
を受けなし、乾式電子写真用正荷電シアントナ−に関す
るものである。
The present invention relates to a positively charged cyan toner for dry electrophotography, which uses a compound with a strong charge control effect, exhibits sufficient positive polarity even in a small amount, and is not limited by the type of resin used.

すなわち、本発明は、フタロシアニン系顔料および樹脂
とからなる乾式電子写真用トナーにおいて、一般式ただ
し、 R,、R3:日またはCH3、C2日5 R2、R4:CH3またはC2日5 R5、R6:日またはCH3 R7:日またはCI Ae:アニオン で示される化合物を含有することを特徴とする電子写真
用正荷電シアントナーである。
That is, the present invention provides a dry electrophotographic toner comprising a phthalocyanine pigment and a resin having the following general formula: R, R3: day or CH3, C2 day 5 R2, R4: CH3 or C2 day 5 R5, R6: This is a positively charged cyan toner for electrophotography, which is characterized by containing a compound represented by anion or CH3R7: day or CI Ae: anion.

上記一般式に入る化合物としては例えば下記の如きもの
がある。
Examples of compounds that fall into the above general formula include the following.

(商品名:NZEN鞠sicCyanine的日、保土
谷化学工業■製)(商品名:Prim比蛇ni肥BXc
onc.住友化学工業■製)(商品名:山ZENDia
mondGreenGH 保±谷化学工業欄製)これら
は一例であって、勿論この他にも上記一般式に入る化合
物ならば本発明に適用可能である。
(Product name: NZEN MarisicCyanine, made by Hodogaya Chemical Industry ■) (Product name: Prim Hibi Nihi BXc
onc. Manufactured by Sumitomo Chemical Co., Ltd.) (Product name: YamaZENDia)
mondGreenGH (manufactured by Hoya Kagaku Kogyo Co., Ltd.)) These are just examples, and of course other compounds that fall into the above general formula can be applied to the present invention.

かかる化合物のトナ−中における含有量は樹脂量の1の
重量%以下で好ましくは5%以下が良い。
The content of such a compound in the toner is 1% by weight or less, preferably 5% or less based on the amount of resin.

また、この化合物は耐光性が著しく弱いため、トナーの
着色剤として単独で使用することは難しく、シアントナ
ーとしての色調を得るための着色剤としてはフタロシア
ニンフルー系顔料を用いるのが良く、これは耐光性がき
わめて強く、透明性、色調も優れている。したがって、
上記一股式で表わされる化合物は正荷電制御剤として使
用することが主目的であり、耐光性が弱くても、主要構
成成分として使用するフタロシアニン系顔料の耐光性が
強いため、コピー後のトナー画像(シアン色)は、本化
合物の荷電制御剤の色が腿色しても問題はない。
In addition, this compound has extremely low light resistance, so it is difficult to use it alone as a coloring agent for toners, so it is better to use phthalocyanine pigments as a coloring agent to obtain the color tone of cyan toner. It has extremely strong light resistance, transparency, and color tone. therefore,
The main purpose of the compound represented by the above single-pronged formula is to be used as a positive charge control agent. There is no problem with the image (cyan color) even if the color of the charge control agent of the present compound is thigh color.

また、保存性については、トナ−および現像剤は一般に
ボルト中で保存するため、保存中に光により本化合物が
化学変化を生じ、荷電制御効果に劣化を生じることはな
い。本発明における樹脂としては、通常の乾式トナ一に
使用されるものであればすべて使用できるが一般には、
荷電制御特性以外の乾式シアントナー用としての性質例
えば樹脂自体の着色、透明性、接着性、流動性、粉砕性
等を考慮して選択すれば良い。
Regarding storage stability, since toners and developers are generally stored in a bolt, the present compound will not undergo chemical changes due to light during storage, and the charge control effect will not deteriorate. As the resin in the present invention, any resin used in ordinary dry toners can be used, but in general,
The selection may be made in consideration of properties for dry cyan toner other than charge control properties, such as coloration, transparency, adhesiveness, fluidity, and pulverizability of the resin itself.

例えばスチレン系樹脂、ヱポキシ系樹脂、フェノール系
樹脂などであるが、上記化合物と併用した場合特に好ま
しい正荷電性が得られるのはスチレン系樹脂である。本
発明のトナーは電子写真カラー複写機の3原色用に用い
るのに特に効果的である。
For example, styrene resins, epixy resins, phenol resins, etc. are used, but styrene resins provide particularly preferable positive chargeability when used in combination with the above compounds. The toner of the present invention is particularly effective for use in the three primary colors of electrophotographic color copying machines.

つぎに実施例並びに試験結果を示す。Next, examples and test results will be shown.

実施例 1 ポリスチレン(商品名:ピコラスチツクD−125エッ
ソスタンダード石油■製) 10の重量部フタロシ
アニン(商品名:リオノールフルーKL東洋インキ製造
■製) 5重量部NZENBasicCya
nine的日(保±谷化学工業■製)
3重量部以上のものをロールミルで溶
融涙練し、冷却後ジェットミルを用いて粗粉砕し、つい
でエアージェット方式による微粉砕機で微粉砕する。
Example 1 Polystyrene (trade name: Picolastik D-125 manufactured by Esso Standard Oil ■) 10 parts by weight Phthalocyanine (trade name: Lionol Flu KL manufactured by Toyo Ink Manufacturing ■) 5 parts by weight NZENBasicCya
nine days (manufactured by Hoya Chemical Industry)
3 parts by weight or more is melted and kneaded in a roll mill, cooled and coarsely ground using a jet mill, and then finely ground using an air jet type pulverizer.

得られた徴粉体を分級して5〜2坪の粒子を得てトナ−
とした。このトナー3重量部に対し、キャリア鉄粉(E
FV150〜250メッシュ、日本鉄粉社製)97重量
部を混合して現像剤とした。
The obtained characteristic powder is classified to obtain particles of 5 to 2 tsubo and used as toner.
And so. Carrier iron powder (E
A developer was prepared by mixing 97 parts by weight of FV150-250 mesh (manufactured by Nippon Tetsuko Co., Ltd.).

この現像剤を用い市販の酸化亜鉛感光体を使用したプレ
ンペーパー複写機を用い現像を行った結果、カブリのな
い鮮明なポジのシアン画像が得られた。
When this developer was used for development using a plain paper copying machine using a commercially available zinc oxide photoreceptor, a clear positive cyan image without fog was obtained.

トナーの帯電量は、市販のブローオフ粉体帯電測定装置
によって測定した結果+5.2山c′夕であった。実施
例 2 スチレンーアクリル酸共重合体(商品名:ハィマーSB
M73三洋化成■製) 10の重量部フタロ
シアニンフルー(商品名:リオノールフルーKL 東洋
インキ製造■製) 5重量部Primoc渡n
ineBXconc.(住友化学工業■製)4重量部以
上のものを実施例1と同様に混合してトナーとした。
The charge amount of the toner was measured using a commercially available blow-off powder charge measuring device and was found to be +5.2 m/c'. Example 2 Styrene-acrylic acid copolymer (product name: Heimer SB
M73 (manufactured by Sanyo Chemical) 10 parts by weight Phthalocyanine Flue (product name: Lionor Flu KL manufactured by Toyo Ink Manufacturing) 5 parts by weight Primoc
ineBXconc. (manufactured by Sumitomo Chemical Co., Ltd.) 4 parts by weight or more were mixed in the same manner as in Example 1 to prepare a toner.

このトナーを用いて、同じく実施例1と同様に試験をし
たところカブリのない鮮明なポジのシアン画像が得られ
た。トナーの帯電量は十6.秋c/夕であった。実施例
3 スチレソーアクリル酸共重合体(商品名:/・ィマーS
BM73 三洋化成■製) 10の重量部フ
タロシアニンフルー(商品名:フタロシアニンフルーL
BG 住友化学工業■製) 5重量部MZENDi
amondGreenGH(保土谷化学工業欄製)
2重量部以上のものを実施
例1と同様に混合してトナーとした。
Using this toner, a test was conducted in the same manner as in Example 1, and a clear positive cyan image without fogging was obtained. The amount of charge on the toner is 16. It was autumn/evening. Example 3 Styresoacrylic acid copolymer (trade name: /・Imer S
BM73 (manufactured by Sanyo Chemical) 10 parts by weight Phthalocyanine Fluoride (Product name: Phthalocyanine Fluorine L)
BG manufactured by Sumitomo Chemical Co., Ltd.) 5 parts by weight MZENDi
amondGreenGH (manufactured by Hodogaya Chemical Co., Ltd.)
2 parts by weight or more were mixed in the same manner as in Example 1 to prepare a toner.

このトナーを用いて同じく実施例1と同様に試験をした
ところカブリのない鮮明なポジのシアン画像が得られた
When this toner was tested in the same manner as in Example 1, a clear positive cyan image without fogging was obtained.

Claims (1)

【特許請求の範囲】 1 フタロシアニン系顔料および樹脂とからなる乾式電
子写真用シアントナーにおいて、一般式▲数式、化学式
、表等があります▼ ただし、 R_1、R_3:HまたはCH_3、C_2H_5R_
2、R_4:CH_3またはC_2H_5R_5、R_
6:HまたはCH_3R_7:HまたはCl A■:アニオン で示される化合物を含有することを特徴とする電子写真
用正荷電シアントナー。
[Claims] 1. A cyan toner for dry electrophotography consisting of a phthalocyanine pigment and a resin, which has a general formula ▲ mathematical formula, chemical formula, table, etc. ▼ However, R_1, R_3: H or CH_3, C_2H_5R_
2, R_4: CH_3 or C_2H_5R_5, R_
6:H or CH_3R_7:H or Cl A■: A positively charged cyan toner for electrophotography, characterized by containing a compound represented by anion.
JP52151823A 1977-12-19 1977-12-19 Positively charged cyan toner for electrophotography Expired JPS6040020B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP52151823A JPS6040020B2 (en) 1977-12-19 1977-12-19 Positively charged cyan toner for electrophotography

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP52151823A JPS6040020B2 (en) 1977-12-19 1977-12-19 Positively charged cyan toner for electrophotography

Publications (2)

Publication Number Publication Date
JPS5484732A JPS5484732A (en) 1979-07-05
JPS6040020B2 true JPS6040020B2 (en) 1985-09-09

Family

ID=15527086

Family Applications (1)

Application Number Title Priority Date Filing Date
JP52151823A Expired JPS6040020B2 (en) 1977-12-19 1977-12-19 Positively charged cyan toner for electrophotography

Country Status (1)

Country Link
JP (1) JPS6040020B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6215113U (en) * 1985-07-09 1987-01-29

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59100453A (en) * 1982-11-30 1984-06-09 Mita Ind Co Ltd Negative-polar color toner
US4539284A (en) * 1984-04-16 1985-09-03 Xerox Corporation Developer compositions with infrared absorbing additives
DE3641525A1 (en) * 1986-12-05 1988-06-16 Hoechst Ag BLUE COLOR FOR ELECTROPHOTOGRAPHIC RECORDING METHOD WITH POSITIVE CONTROL EFFECT
US7442481B2 (en) 2004-04-27 2008-10-28 Xsys Print Solutions Us Llc Charge control agent

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6215113U (en) * 1985-07-09 1987-01-29

Also Published As

Publication number Publication date
JPS5484732A (en) 1979-07-05

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