JP3098595B2 - Non-magnetic one-component development method - Google Patents

Non-magnetic one-component development method

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Publication number
JP3098595B2
JP3098595B2 JP03334624A JP33462491A JP3098595B2 JP 3098595 B2 JP3098595 B2 JP 3098595B2 JP 03334624 A JP03334624 A JP 03334624A JP 33462491 A JP33462491 A JP 33462491A JP 3098595 B2 JP3098595 B2 JP 3098595B2
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JP
Japan
Prior art keywords
toner
developer
magnetic
weight
vinyl
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 - Fee Related
Application number
JP03334624A
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Japanese (ja)
Other versions
JPH05165253A (en
Inventor
敏 竹澤
安成 中村
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.)
Fujitsu Ltd
Original Assignee
Fujitsu Ltd
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Priority to JP03334624A priority Critical patent/JP3098595B2/en
Publication of JPH05165253A publication Critical patent/JPH05165253A/en
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Expired - Fee Related legal-status Critical Current

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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、電子写真複写機、電子
写真プリンタなどに用いられる非磁性一成分現像方法に
関する。電子写真法としては米国特許第2297691
号などに記載された方式が周知であるが、これは、一般
には光導電性絶縁体(感光体ドラムなど)を利用し、コ
ロナ放電などにより光導電性絶縁体上に一様な静電荷を
与え、様々な手段により光導電性絶縁体上に光像を照射
することによって静電潜像を形成し、次いで、潜像をト
ナーと呼ばれる微粉末を用いて現像可視化し、必要に応
じて紙等にトナー画像を転写した後、加圧、加熱、溶剤
蒸気、光等によりトナー画像を溶融させて紙等に定着さ
せ、印刷物を得るものである。これらの静電潜像を現像
するトナーとしては、従来より天然または合成高分子物
質よりなるバインダ樹脂中に染料、カーボンブラックな
どの着色剤等を分散させたものを1〜30μm程度に微
粉砕した粒子が用いられていた。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a non-magnetic one-component developing method used for an electrophotographic copying machine, an electrophotographic printer and the like. US Pat. No. 2,297,691 describes electrophotography.
In general, a method described in Japanese Patent Application Laid-Open No. H10-26095 is known, which uses a photoconductive insulator (photosensitive drum or the like) and applies a uniform electrostatic charge on the photoconductive insulator by corona discharge or the like. To form an electrostatic latent image by irradiating a photo image on the photoconductive insulator by various means, and then visualize the latent image with a fine powder called toner, and, if necessary, paper. After the transfer of the toner image, the toner image is melted by pressurizing, heating, solvent vapor, light, or the like and fixed on paper or the like to obtain a printed matter. As a toner for developing these electrostatic latent images, a dispersion of a coloring agent such as a dye and carbon black in a binder resin composed of a natural or synthetic polymer substance is conventionally pulverized to about 1 to 30 μm. Particles were used.

【0002】かかるトナーは通常、トナー単体もしくは
鉄粉、ガラスビーズなどの担体物質(キャリア)と混合
され、静電潜像の現像に用いられる。トナー単体で現像
に供せられた場合(非磁性一成分現像方法)、トナーは
層厚規制ブレードや現像器内の各部材と摩擦帯電された
後現像ローラによって運搬され、光導電性絶縁体上の潜
像部分と接触させることによって可視像を形成する。
Such a toner is usually used alone or mixed with a carrier substance (carrier) such as iron powder or glass beads and used for developing an electrostatic latent image. When the toner alone is used for development (non-magnetic one-component developing method), the toner is frictionally charged with the layer thickness regulating blade and each member in the developing device, and then transported by the developing roller, and is transferred onto the photoconductive insulator. A visible image is formed by contacting the latent image portion of the image.

【0003】[0003]

【従来の技術および発明が解決しようとする課題】しか
しながら、このような従来の非磁性一成分現像法にあっ
ては、層厚規制装置を用いて現像剤担持体に付着させる
トナー量を規制しており、トナーとしてはスチレン−ア
クリル等の樹脂に着色剤などを分散させ、粉砕したトナ
ーを用いていた。粉砕法によって製造したトナーは形状
が不定形となり、トナーの形状は鋭角部が多いものとな
る。
However, in such a conventional non-magnetic one-component developing method, the amount of toner adhered to a developer carrier is regulated by using a layer thickness regulating device. As the toner, a colorant or the like is dispersed in a resin such as styrene-acryl or the like, and a pulverized toner is used. The toner produced by the pulverization method has an irregular shape, and the shape of the toner has many sharp corners.

【0004】非磁性一成分現像法は、層厚規制ブレード
との強力な摩擦によって瞬時に帯電させるため、トナー
にかかる圧力は非常に大きくなる。このストレスによっ
てトナーは鋭角部分から破砕され、生じた微粉が層厚規
制ブレードをすり抜けやすくなり摩擦帯電効率が低下
し、トナー帯電量が低下することから印字濃度が低下し
たり、無帯電トナーが増加することでかぶりが増え印字
品位が劣化することが大きな問題となっていた。
In the non-magnetic one-component developing method, the toner is charged instantly by strong friction with a layer thickness regulating blade, so that the pressure applied to the toner becomes extremely large. Due to this stress, the toner is crushed from an acute angle portion, and the generated fine powder easily slips through the layer thickness regulating blade, lowering the triboelectric charging efficiency, and lowering the toner charge amount, thereby lowering the print density and increasing the amount of uncharged toner. This causes a large problem that fog increases and print quality deteriorates.

【0005】本発明は、このような従来の問題点に鑑み
てなされたものであって、トナーの形状の鋭角部分をな
くし、帯電量の低下、印字濃度の低下を防止すること
で、長時間連続印刷を行っても印字品位が高く、画像変
化を起こさない非磁性一成分現像方法を提供することを
目的とする。
SUMMARY OF THE INVENTION The present invention has been made in view of such conventional problems, and eliminates an acute angle portion of a toner shape, thereby preventing a decrease in charge amount and a decrease in print density, thereby prolonging a long time. It is an object of the present invention to provide a non-magnetic one-component developing method which has high print quality even when continuous printing is performed and does not cause an image change.

【0006】[0006]

【課題を解決するための手段】非磁性一成分現像方法に
おいては、(1)層厚規制ブレードのストレスによりト
ナー破砕が生じないこと、(2)クリーニングブレード
でブレードをすりぬけることなく確実にクリーニングさ
れなければならないこと、以上のような特性が求められ
ている。
In the non-magnetic one-component developing method, (1) the toner is not crushed due to the stress of the layer thickness regulating blade, and (2) the cleaning is surely performed without rubbing the blade with the cleaning blade. What is necessary is the above-mentioned characteristics.

【0007】上記の特性を満足する方法として(1)層
厚規制ブレードのストレスによるトナー破砕を防止する
ためには、トナーの形状に鋭角部分がないこと、(2)
クリーニングブレードのすりぬけを防止するためには、
トナーが適当な異形化度を有していることなどが考えら
れる。そこで、本発明者らは、これらの特性を満たすた
めに、非磁性一成分現像方法において、(1)乳化重合
法により得られた微小粒子を凝集し、微粒子界面を融着
させ一つのトナーとなる乳化重合粒子凝集法で作成した
トナーを用いる、(2)微粒子界面を融着させる(以
後、熟成という)時間を制御し、トナー形状をワーデル
の球形化度0.90〜0.85の範囲にする。以上のこ
とにより、トナー形状に鋭角部を無くし、さらに適当な
不定形化度を付与することにより層厚規制ブレードのス
トレスで破砕を起こすことなく、しかもクリーニングブ
レードにおいてはすりぬけがおきず、クリーニング不良
を生じることのない非磁性一成分現像方法を発明するに
至った。
As a method satisfying the above characteristics, (1) in order to prevent toner crushing due to stress of the layer thickness regulating blade, there is no acute angle portion in the toner shape;
To prevent the cleaning blade from slipping,
It is possible that the toner has an appropriate degree of deformation. In order to satisfy these characteristics, the inventors of the present invention, in the non-magnetic one-component developing method, (1) agglomerate the fine particles obtained by the emulsion polymerization method, fuse the interface of the fine particles, and form one toner. (2) The time for fusing the interface of the fine particles (hereinafter referred to as aging) is controlled, and the toner shape is in the range of Wader's degree of sphericity of 0.90 to 0.85. To As described above, the sharpness of the toner shape is eliminated, and the appropriate irregularity is imparted, so that the toner is not crushed by the stress of the layer thickness regulating blade. The present invention has led to the invention of a non-magnetic one-component developing method which does not cause any problem.

【0008】ここで述べるワーデルの球形化度とは以下
の式によって算出される。 ワーデルの球形化度=(粒子の投影面積と同じ面積の円
の直径)/(粒子の投影面に外接する円の直径) 次に、乳化重合粒子凝集法によるトナー作製方法につい
て説明する。
The Wardel's degree of sphericity described here is calculated by the following equation. Wardell's degree of sphericity = (diameter of a circle having the same area as the projected area of the particles) / (diameter of a circle circumscribing the projected surface of the particles) Next, a method of producing a toner by an emulsion polymerization particle aggregation method will be described.

【0009】作製方法は特許公開報63−28117
2,63−282749などに詳しいが簡単に説明する
と、まず、モノマ、着色剤等の予備分散を行う。そし
て、この予備分散を行ったモノマ混合物を乳化剤の入っ
た水溶液混合物中に添加し、撹拌を行い乳化微粒子を作
製する。ここに、重合開始剤を添加し、加熱を行いラジ
カル重合反応を行う。この重合温度は50℃以上、一般
的には70〜90℃の温度で行う。この工程で平均粒径
1〜3μmの微粒子を得る。次に、この重合体が分散し
た液を撹拌しながら塩析剤を添加し微粒子を凝集させ、
さらに撹拌を続けながら樹脂のガラス転移点以上の温度
で加熱を行うことにより、微粒子間を融着させ(熟成)
平均粒径5〜20μmのトナーを得る。
The production method is described in Patent Publication 63-28117.
The details will be briefly described in 2, 63-282749 and the like. First, preliminary dispersion of a monomer, a colorant, and the like is performed. Then, the preliminarily dispersed monomer mixture is added to an aqueous solution mixture containing an emulsifier, and the mixture is stirred to produce emulsified fine particles. Here, a polymerization initiator is added, and the mixture is heated to perform a radical polymerization reaction. The polymerization is carried out at a temperature of 50 ° C. or higher, generally 70 to 90 ° C. In this step, fine particles having an average particle size of 1 to 3 μm are obtained. Next, a salting-out agent was added while stirring the liquid in which the polymer was dispersed to aggregate fine particles,
Further, by heating at a temperature equal to or higher than the glass transition point of the resin while continuing stirring, the particles are fused together (aging).
A toner having an average particle size of 5 to 20 μm is obtained.

【0010】熟成終了後、生成物を洗浄、濾過デカンテ
ーション等適当な方法により回収し、乳化重合粒子凝集
法トナーを得る。本発明において用いられるモノマは当
然スチレン−アクリルに限定されるものではなく、一分
子中にエチレン性不飽和結合を一つ有するモノマであれ
ばよい。例えば、スチレン、o−メチルスチレン、m−
メチルスチレン、p−メチルスチレン、p−メトキシス
チレン、p−フェニルスチレン、p−クロルスチレン、
3,4-ジクロルスチレン、p−エチルスチレン、2,4-ジメ
チルスチレン、p-n-ブチルスチレン、 p-tert-ブチルス
チレン、p-n-ノニルスチレン、p-n-オクチルスチレン、
p-n-ヘキシルスチレン、p-n-ドデシルスチレン等のスチ
レンおよびその誘導体、エチレン、プロピレン、ブチレ
ン、イソブチレン等のエチレン不飽和モノオレフィン
類、塩化ビニル、塩化ビニリデン、臭化ビニル、フッ化
ビニル等のハロゲン化ビニル類、酢酸ビニル、プロピオ
ン酸ビニル、ベンゾイル酸ビニル等のビニルエステル
類、メタクリル酸メチル、メタクリル酸エチル、メタク
リル酸プロピル、メタクリル酸n-ブチル、メタクリル酸
イソブチル、メタクリル酸n-オクチル、メタクリル酸ド
デシル、メタクリル酸-2- エチルヘキシル、メタクリル
酸ステアリル、メタクリル酸フェニル、メタクリル酸ジ
メチルアミノエチル、メタクリル酸ジエチルアミノエチ
ル等のα−メチレン脂肪酸モノカルボン酸エステル類、
アクリル酸メチル、アクリル酸エチル、アクリル酸n-ブ
チル、アクリル酸イソブチル等のアクリル酸エステル
類、ビニルメチルエーテル、ビニルエチルエーテル、ビ
ニルイソブチルエーテル等のビニルエーテル類、ビニル
メチルケトン、ビニルヘキシルケトン、メチルイソプロ
ペニルケトン等のビニルケトン類、N-ビニルピロール、
N-ビニカルバゾール、N-ビニルインドール、N-ビニルピ
ロリドン等のn-ビニル化合物、ビニルナフタリン類、ア
クリロニトリル、メタクリロニトリル、アクリルアミド
等アクリル酸もしくはメタクリル酸誘導体等がある。こ
れらは、単独もしくは混合して用いることができる。
After the aging, the product is recovered by a suitable method such as washing, filtration and decantation to obtain an emulsion polymerized particle aggregation method toner. The monomer used in the present invention is not limited to styrene-acryl, but may be any monomer having one ethylenically unsaturated bond in one molecule. For example, styrene, o-methylstyrene, m-
Methylstyrene, p-methylstyrene, p-methoxystyrene, p-phenylstyrene, p-chlorostyrene,
3,4-dichlorostyrene, p-ethylstyrene, 2,4-dimethylstyrene, pn-butylstyrene, p-tert-butylstyrene, pn-nonylstyrene, pn-octylstyrene,
Styrene and its derivatives such as pn-hexylstyrene and pn-dodecylstyrene; ethylenically unsaturated monoolefins such as ethylene, propylene, butylene and isobutylene; vinyl halide such as vinyl chloride, vinylidene chloride, vinyl bromide and vinyl fluoride , Vinyl acetate, vinyl propionate, vinyl esters such as vinyl benzoylate, methyl methacrylate, ethyl methacrylate, propyl methacrylate, n-butyl methacrylate, isobutyl methacrylate, n-octyl methacrylate, dodecyl methacrylate, Α-methylene fatty acid monocarboxylic acid esters such as 2-ethylhexyl methacrylate, stearyl methacrylate, phenyl methacrylate, dimethylaminoethyl methacrylate, and diethylaminoethyl methacrylate;
Acrylic esters such as methyl acrylate, ethyl acrylate, n-butyl acrylate and isobutyl acrylate; vinyl ethers such as vinyl methyl ether, vinyl ethyl ether and vinyl isobutyl ether; vinyl methyl ketone, vinyl hexyl ketone and methyl iso Vinyl ketones such as propenyl ketone, N-vinyl pyrrole,
Examples include n-vinyl compounds such as N-vinylcarbazole, N-vinylindole, and N-vinylpyrrolidone, and acrylic or methacrylic acid derivatives such as vinylnaphthalenes, acrylonitrile, methacrylonitrile, and acrylamide. These can be used alone or as a mixture.

【0011】乳化剤としては、公知の乳化剤、例えば石
鹸、カチオン活性剤、アニオン活性剤、フッソ活性剤等
が使用し得る。一般にこれらの乳化剤の使用量は、水に
対して0.01〜1重量%(さらに好ましくは、0.1
〜0.5重量%)が好ましい。次に、重合開始剤として
は、公知の熱重合開始剤、例えば過硫酸カリウム等の過
硫酸塩、アゾビスイソブチロニトリル、ベンゾイルパー
オキサイド、メチルエチルケトンパセーオキサイド、イ
ソプロピルパーオキシカーボネート等、さらにはレドッ
クス系の開始剤を使用しても重合を行わせることができ
る。通常、これらの重合開始剤の使用量は、一般に重合
性混合物の重量の約0.01〜10%(より好ましくは
0.05〜5重量%)で充分である。
As the emulsifier, a known emulsifier, for example, a soap, a cationic activator, an anionic activator, a fluorine activator and the like can be used. Generally, these emulsifiers are used in an amount of 0.01 to 1% by weight relative to water (more preferably 0.1 to 1% by weight).
-0.5% by weight). Next, as the polymerization initiator, known thermal polymerization initiators, for example, persulfates such as potassium persulfate, azobisisobutyronitrile, benzoyl peroxide, methyl ethyl ketone passoxide, isopropyl peroxycarbonate, etc. Polymerization can also be carried out using a redox initiator. Generally, the amount of the polymerization initiator used is generally about 0.01 to 10% (more preferably 0.05 to 5% by weight) of the weight of the polymerizable mixture.

【0012】着色剤としては、公知の顔料、および染料
が使用できる。例えば、黒色顔料としては、チャネルブ
ラック、ファーネスブラック等があり、着色顔料として
は、カドミウムイエロー、ピラゾロンレッド、フタロシ
アニンブルーB、フタロシアニングリーン等がある。染
料としては、C.Iダイレクトレッド1、C.Iダイレ
クトブルー1等がある。
As the coloring agent, known pigments and dyes can be used. For example, black pigments include channel black and furnace black, and coloring pigments include cadmium yellow, pyrazolone red, phthalocyanine blue B, phthalocyanine green, and the like. As the dye, C.I. I Direct Red 1, C.I. I Direct Blue 1 and others.

【0013】さらに、トナー原料成分の中には、必要に
応じて帯電制御剤、流動性改質剤等の添加剤を加えても
よい。
Further, additives such as a charge control agent and a fluidity modifier may be added to the toner raw material components as required.

【0014】[0014]

【作用】鋭意研究の結果、乳化微粒子凝集法で作製した
トナーの形状をワーデルの球形化度0.90〜0.85
に制御することにより、トナーが層厚規制ブレードのス
トレスで破砕を生じることがなく、さらに良好なクリー
ニング性を示すことで高印字品位を長期保持することを
可能とした。これは、(1)トナー表面に鋭角部が存在
しないことから、層厚規制ブレードによって破砕されな
い、(2)トナー形状が真球状ではなく一定以上の不定
形化度を有しているため、トナーとクリーニングブレー
ドとの接触面積が大きくなりクリーニングブレードで完
全に回収されること等が原因として考えられる。
As a result of intensive studies, it was found that the toner produced by the emulsified fine particle agglomeration method had a Wardel sphericity of 0.90 to 0.85.
In this manner, the toner is not crushed by the stress of the layer thickness regulating blade, and the high printing quality can be maintained for a long period of time by exhibiting better cleaning properties. This is because (1) the toner surface is not crushed by the layer-thickness regulating blade because there is no acute-angled portion, and (2) the toner shape is not a true sphere but has a certain degree of irregularity. It is considered that the contact area between the cleaning blade and the cleaning blade becomes large and the cleaning blade completely collects the cleaning blade.

【0015】[0015]

【実施例】以下、本発明を実施例によりさらに具体的に
説明するが、これにより限定されるものでない。まず、
本発明の非磁性一成分現像方法を実施するための電子写
真記録装置を説明する。
EXAMPLES Hereinafter, the present invention will be described more specifically with reference to Examples, but it should not be construed that the invention is limited thereto. First,
An electrophotographic recording apparatus for performing the non-magnetic one-component developing method of the present invention will be described.

【0016】図1において、現像剤1の貯蔵手段2と、
現像剤1を現像領域を含む所定の循環経路に沿って搬送
する現像剤担持体3との間に、表面部に可塑材が被着さ
れたローラ状の現像剤回収手段4を前記現像剤担持体3
に接触するように設ける。そして、前記現像剤担持体3
と前記現像剤回収手段4との間に、現像剤1が前記現像
剤担持体3から前記現像剤回収手段4に向かう方向にバ
イアス電圧(以後、回収バイアスとする)を印加する。
これは、接触による機械的な回収のみならず、回収バイ
アスによる電気的な回収を行うことによって、安定かつ
確実に前記現像剤担持体3上の機械的かつ電気的な履歴
を解消するためである。そこで新たに、前記現像剤担持
体3に接触しつつ前記貯蔵手段2に貯蔵されている現像
剤1を前記現像剤担持体3に供給し、機械的な摩擦によ
り現像剤を帯電させ、帯電トナー層を前記現像剤担持体
3上に形成し、層厚規制ブレード5によりその層厚を所
望の厚さに規制した後現像領域に搬送し現像を行う。
In FIG. 1, storage means 2 for developer 1
A roller-shaped developer collecting unit 4 having a plastic material adhered to the surface thereof is provided between the developer carrier 3 and the developer carrier 3 which transports the developer 1 along a predetermined circulation path including a developing area. Body 3
It is provided so as to come into contact with. And the developer carrier 3
A bias voltage (hereinafter referred to as a collection bias) is applied between the developer 1 and the developer collection unit 4 in a direction from the developer carrier 3 toward the developer collection unit 4.
This is because the mechanical and electrical history on the developer carrier 3 is stably and surely eliminated by performing not only mechanical recovery by contact but also electrical recovery by a recovery bias. . Therefore, the developer 1 stored in the storage unit 2 is newly supplied to the developer carrier 3 while being in contact with the developer carrier 3, and the developer is charged by mechanical friction. A layer is formed on the developer carrying member 3, the layer thickness is regulated to a desired thickness by a layer thickness regulating blade 5, and the layer is conveyed to a development area to perform development.

【0017】6は潜像担持体であり、表面に形成された
潜像を現像部に搬送し、できた現像剤の像を記録用紙に
転写する位置に搬送するものである。この潜像担持体6
には、潜像形成方式によって光導電材料である感光体
(有機感光体、セレン感光体、アモルファスシリコン感
光体等)や絶縁体を用いることができる。また、ここで
用いる現像剤担持体3は3〜20μmの気孔を持つ多孔
質ポリウレタンで形成し、10μm前後のトナーが侵入
しないようにした。我々の実験では、多孔質の状態が、
それぞれ連続する連泡状態においても、気孔の大きさを
20μm以下にするとトナーが、気孔内で互いに支え合
い侵入しない事を確認した。また、20μm以上の気孔
になると、単泡にすればトナーの侵入を防ぐことはでき
るが、凹部において、潜像と導電体(この場合スポンジ
自身)の距離が離れ、その部分のトナーに現像バイアス
がかからなくなり、スポンジの凹部に応じた低濃度部が
印字に表れる。従って、気孔部は、20μm以下の大き
さが望ましい。また、スポンジの体積抵抗値は104
1010Ωcmの範囲が望ましく電気抵抗値が低くなる
と、層厚規制ブレード5へ大電流が流れ込みジュール熱
が発生し、現像剤担持体3が焼損する。また、現像剤担
持体表面硬度はアスカーC硬度計で50°以下とした。 実施例1 モノマ スチレン(和光純薬製) 90重量部 ブチルアクリレート(和光純薬製) 10重量部 n-ブチルメタクリレート(和光純薬製) 5重量部 着色剤 カーボンブラック(150T,デグザ社製) 2重量部 アゾクロム染料(S:34,オリエント社製) 2重量部 乳化剤 ネオゲンSC(第一工業製薬製) 0.2重量部 熱重合開始剤 ベンゾイルパーオキサイド 0.2重量部 塩析剤 10%食塩水 0.05重量部 外添剤 疎水性シリカ H−2000(ヘキスト社製) 0.5重量部 上記モノマ、着色剤をディスパーサー(ヤマト科学製)
を用い、3分間撹拌しモノマ混合物を調整した。つぎ
に、重合開始剤、乳化剤を添加した蒸留水500重量部
中にこのモノマ混合物を入れ、室温(20度)でディス
パーサー(4,000r.p.m )を用いて3分間撹拌し
た。その後ディスパーサーをスリーワンモーターに変
え、100r.p.m にて撹拌しながら60℃に加熱し、完
全にモノマ混合物を重合させた。次に、水に分散した生
成微粒子に塩析剤を滴下し、100℃に加熱して顕微鏡
観察下でトナーがワーデルの球形化度0.90になるま
で熟成を続けた。ここで、ワーデルの球形化度は、顕微
鏡写真で任意に100個のトナーを選びだし、トナーに
外接する円と、トナーと同面積の円の直径を目測により
測定し算出した。次に、水に分散したトナーを遠心分離
し、ろ別した。このトナーをphが8以下になるまで水
洗を繰り返しトナーを得た。このトナーに流動性改質剤
として疎水性シリカを0.5重量部添加した。
Reference numeral 6 denotes a latent image carrier, which conveys the latent image formed on the surface to the developing section and conveys the formed developer image to a position where the image is transferred to recording paper. This latent image carrier 6
A photoconductor (organic photoconductor, selenium photoconductor, amorphous silicon photoconductor, or the like) or an insulator that is a photoconductive material can be used depending on the latent image forming method. The developer carrier 3 used here is formed of porous polyurethane having pores of 3 to 20 μm so that toner of about 10 μm does not enter. In our experiments, the porous state
It was confirmed that, even in the continuous bubble state, when the pore size was set to 20 μm or less, the toners supported each other in the pores and did not enter. When the pores have a size of 20 μm or more, the intrusion of toner can be prevented by forming a single cell. However, the distance between the latent image and the conductor (in this case, the sponge itself) is large in the concave portion, and the toner in that portion has a developing bias. , And a low density portion corresponding to the concave portion of the sponge appears on the print. Therefore, the pore size is desirably 20 μm or less. The volume resistance of the sponge is 10 4 to
When the electric resistance value is desirably in the range of 10 10 Ωcm, a large current flows into the layer thickness regulating blade 5 to generate Joule heat and burn the developer carrier 3. The surface hardness of the developer carrier was set to 50 ° or less by an Asker C hardness meter. Example 1 Monomer Styrene (manufactured by Wako Pure Chemical) 90 parts by weight Butyl acrylate (manufactured by Wako Pure Chemical) 10 parts by weight n-butyl methacrylate (manufactured by Wako Pure Chemical) 5 parts by weight Colorant carbon black (150T, manufactured by Degussa) 2 Parts by weight Azochrome dye (S: 34, manufactured by Orient) 2 parts by weight Emulsifier Neogen SC (manufactured by Daiichi Kogyo Seiyaku) 0.2 parts by weight Thermal polymerization initiator benzoyl peroxide 0.2 parts by weight Salting-out agent 10% saline 0.05 parts by weight External additive Hydrophobic silica H-2000 (manufactured by Hoechst) 0.5 parts by weight Disperser (manufactured by Yamato Scientific Co., Ltd.)
The mixture was stirred for 3 minutes to prepare a monomer mixture. Next, this monomer mixture was put into 500 parts by weight of distilled water to which a polymerization initiator and an emulsifier had been added, and stirred at room temperature (20 ° C.) for 3 minutes using a disperser (4,000 rpm). Thereafter, the disperser was changed to a three-one motor and heated to 60 ° C. while stirring at 100 rpm to completely polymerize the monomer mixture. Next, a salting-out agent was added dropwise to the resulting fine particles dispersed in water, heated to 100 ° C., and ripened under a microscope until the toner had a Wardel sphericity of 0.90. Here, the spherical degree of Wardell was calculated by arbitrarily selecting 100 toners from a micrograph and measuring the diameters of a circle circumscribing the toner and a circle having the same area as the toner by visual measurement. Next, the toner dispersed in water was centrifuged and separated by filtration. This toner was repeatedly washed with water until ph became 8 or less to obtain a toner. To this toner, 0.5 parts by weight of hydrophobic silica was added as a fluidity modifier.

【0018】このトナー200gを前記装置(20枚/
分)に搭載し、連続印字テストを行い印字品位、および
現像剤担持体上のトナーの粒径分布、クリーニング性の
変化を調べた。結果、10万枚の連続印字後も印字品
位、トナーの粒径分布、クリーニング性には全く問題な
かった。 実施例2 実施例1と同様の方法により乳化微粒子を作製し、塩析
剤を添加したのち100℃に加熱してワーデルの球形化
度が0.85になるまで熟成を行った。さらに実施例1
と同様の処理を施しトナーを作製し、前記装置により1
0万枚の連続印字試験を行った。
200 g of the toner is applied to the above-mentioned apparatus (20 sheets /
), And a continuous printing test was performed to examine the print quality, the particle size distribution of the toner on the developer carrying member, and the change in cleaning performance. As a result, even after continuous printing of 100,000 sheets, there was no problem in print quality, toner particle size distribution, and cleaning property. Example 2 Emulsified fine particles were prepared in the same manner as in Example 1, and after addition of a salting-out agent, the mixture was heated to 100 ° C. and aged until the Wardel sphericity was 0.85. Example 1
The same process as described above is performed to produce a toner.
A continuous printing test of 100,000 sheets was performed.

【0019】結果、試験後も印字品位、トナーの粒径分
布、クリーニング性には全く問題なかった。 比較例1 バインダ樹脂 スチレンアクリル樹脂(Tg=60℃,軟化点=140℃) 95重量部 着色剤 カーボンブラック(150T,デグザ社製) 2重量部 アゾクロム染料(S:34,オリエント社製) 2重量部 外添剤 疎水性シリカ(H−2000,ヘキスト社製) 0.5重量部 バインダ樹脂と着色剤を混合した後溶融混練し、得られ
た樹脂塊をロートプレックスにより粗粉砕した後、ジェ
ットミル(PJM粉砕機、日本ニューマチック工業製)
を用いて微粉砕を行い、粉砕物を風力分級機(アルピネ
社製)により分級し、ワーデルの球形化度が0.64の
トナーを得た。このトナーに流動性改質として疎水性シ
リカを0.5重量部添加し現像剤とし、前記装置により
10万枚の連続印刷試験を行った。
As a result, there was no problem in print quality, toner particle size distribution, and cleaning property even after the test. Comparative Example 1 Binder resin Styrene acrylic resin (Tg = 60 ° C., softening point = 140 ° C.) 95 parts by weight Colorant carbon black (150T, manufactured by Degussa) 2 parts by weight Azochrome dye (S: 34, manufactured by Orient) 2 parts by weight Part External additive Hydrophobic silica (H-2000, manufactured by Hoechst) 0.5 part by weight After mixing the binder resin and the coloring agent, they are melt-kneaded, and the obtained resin mass is roughly pulverized by a rotoplex, and then jet-milled. (PJM crusher, manufactured by Nippon Pneumatic Industries)
Then, the pulverized product was classified with an air classifier (manufactured by Alpine) to obtain a toner having a Wardel sphericity of 0.64. To this toner, 0.5 parts by weight of hydrophobic silica was added as a fluidity modifier to prepare a developer, and a continuous printing test of 100,000 sheets was performed using the above apparatus.

【0020】結果、試験後の印字サンプルにおいて『か
すれ』が生じ、かぶりも増加し印字品質が初期と比べて
大きく低下した。また、トナーも5μm以下の微粉が増
加し、粒径分布がブロードとなりドラム上にはクリーニ
ングされないトナー層が形成した。 比較例2 実施例1と同様の方法により乳化微粒子を作製し、塩析
剤を添加したのち100℃に加熱してワーデルの球形化
度が0.78になるまで熟成を行った。さらに実施例1
と同様の処理を施しトナーを作製し、前記装置により1
0万枚の連続印字試験を行った。
As a result, "smearing" occurred in the printed sample after the test, the fog increased, and the printing quality was greatly reduced as compared with the initial stage. In addition, the amount of fine powder having a particle size of 5 μm or less increased, the particle size distribution became broad, and a toner layer that was not cleaned was formed on the drum. Comparative Example 2 Emulsified fine particles were prepared in the same manner as in Example 1, and after adding a salting-out agent, the mixture was heated to 100 ° C. and aged until the Wardel sphericity was 0.78. Example 1
The same process as described above is performed to produce a toner.
A continuous printing test of 100,000 sheets was performed.

【0021】結果、試験後の印字サンプルにおいて『か
すれ』が生じ、かぶりも増加し印字品質が初期と比べて
大きく低下した。また、トナーも5μm以下の微粉が増
加し、粒径分布がブロードとなりドラム上にはクリーニ
ングされないトナー層が形成した。 比較例3 実施例1と同様の方法により乳化微粒子を作製し、塩析
剤を添加したのち100℃に加熱してワーデルの球形化
度が0.96になるまで熟成を行った。さらに実施例1
と同様の処理を施しトナーを作製し、前記装置により印
字試験を行ったところ初期においてクリーニング不良が
発生した。
As a result, "smearing" occurred in the printed sample after the test, the fog increased, and the printing quality was greatly reduced as compared with the initial stage. In addition, the amount of fine powder having a particle size of 5 μm or less increased, the particle size distribution became broad, and a toner layer that was not cleaned was formed on the drum. Comparative Example 3 Emulsified fine particles were prepared in the same manner as in Example 1, and after adding a salting-out agent, the mixture was heated to 100 ° C. and aged until the Wardell's sphericity reached 0.96. Example 1
A toner was prepared by performing the same treatment as described above, and a printing test was performed using the above-described apparatus.

【0022】[0022]

【発明の効果】以上説明してきたように、本発明によれ
ば、帯電特性およびクリーニング性が良好であり、連続
印刷においても印字特性が低下することなく、良好な印
字品質を長期にわたり維持することができる。
As described above, according to the present invention, it is possible to maintain good printing quality for a long period of time without deteriorating the printing characteristics even in continuous printing, having good charging characteristics and cleaning properties. Can be.

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

【図1】電子写真記録装置を示す図FIG. 1 shows an electrophotographic recording apparatus.

【符号の説明】[Explanation of symbols]

1:現像剤 2:貯蔵手段 3:現像剤担持体 4:現像剤回収手段 5:層厚規制ブレード 6:潜像担持体 1: developer 2: storage means 3: developer carrier 4: developer recovery means 5: layer thickness regulating blade 6: latent image carrier

───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 昭60−220358(JP,A) 特開 昭63−235956(JP,A) ──────────────────────────────────────────────────続 き Continuation of the front page (56) References JP-A-60-220358 (JP, A) JP-A-63-235956 (JP, A)

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】潜像担持体に対して現像剤担持体によって
搬送される現像剤を層厚規制部材により摩擦帯電すると
ともに層厚を規制して現像を行う非磁性一成分現像方法
において、 前記現像剤として、乳化重合粒子凝集法により得られ、
そのワーデルの球形化度が0.90〜0.85であるト
ナーを用いることを特徴とする非磁性一成分現像方法。
1. A non-magnetic one-component developing method in which a developer conveyed by a developer carrier to a latent image carrier is frictionally charged by a layer thickness regulating member and development is performed while regulating a layer thickness. As a developer, obtained by emulsion polymerization particle aggregation method,
A non-magnetic one-component developing method using a toner having a Wardel sphericity of 0.90 to 0.85.
JP03334624A 1991-12-18 1991-12-18 Non-magnetic one-component development method Expired - Fee Related JP3098595B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP03334624A JP3098595B2 (en) 1991-12-18 1991-12-18 Non-magnetic one-component development method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP03334624A JP3098595B2 (en) 1991-12-18 1991-12-18 Non-magnetic one-component development method

Publications (2)

Publication Number Publication Date
JPH05165253A JPH05165253A (en) 1993-07-02
JP3098595B2 true JP3098595B2 (en) 2000-10-16

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Country Link
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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3685905B2 (en) * 1997-05-19 2005-08-24 富士ゼロックス株式会社 Method for producing toner for developing electrostatic image, toner for developing electrostatic image, developer for electrostatic image, and image forming method
JP2001296684A (en) * 2000-04-11 2001-10-26 Mitsubishi Chemicals Corp Toner and method for image forming

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60220358A (en) * 1984-04-17 1985-11-05 Hitachi Chem Co Ltd Production of toner for electrophotography
JPH0738079B2 (en) * 1987-03-24 1995-04-26 コニカ株式会社 Electrostatic latent image development method

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