JPS603646A - Production of toner - Google Patents

Production of toner

Info

Publication number
JPS603646A
JPS603646A JP58112221A JP11222183A JPS603646A JP S603646 A JPS603646 A JP S603646A JP 58112221 A JP58112221 A JP 58112221A JP 11222183 A JP11222183 A JP 11222183A JP S603646 A JPS603646 A JP S603646A
Authority
JP
Japan
Prior art keywords
toner
foaming agent
microcapsulated
obtd
solvent
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.)
Pending
Application number
JP58112221A
Other languages
Japanese (ja)
Inventor
Takeshi Saikawa
済川 健
Takeshi Hashimoto
健 橋本
Naoya Yabuuchi
尚哉 薮内
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.)
Fujifilm Business Innovation Corp
Original Assignee
Fuji Xerox 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 Fuji Xerox Co Ltd filed Critical Fuji Xerox Co Ltd
Priority to JP58112221A priority Critical patent/JPS603646A/en
Publication of JPS603646A publication Critical patent/JPS603646A/en
Pending legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00Developers
    • G03G9/08Developers with toner particles
    • G03G9/0802Preparation methods
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00Developers
    • G03G9/08Developers with toner particles
    • G03G9/0825Developers with toner particles characterised by their structure; characterised by non-homogenuous distribution of components

Abstract

PURPOSE:To obtain a toner which is easy to grind and produce and has good electrostatic charge exchangeable, developing and transfer characteristics and excellent fixability by adding a microcapsulated foaming agent to a toner raw material and kneading the mixture thereof. CONSTITUTION:A microcapsuled foaming agent, more particularly, a solvent type foaming agent is added to a toner raw material and the mixture thereof is kneaded. A microcapsulated foaming agent or the like consisting of, for example, n-hexane, etc. as a core and having a polyurethane wall formed by an interfacial polymn. method, etc. is used for such microcapsulated solvent type foaming agent. A slab having numerous foam is obtd. by kneading such foaming agent with the other toner raw material. Such slab is easily ground as it is porous and the toner having much micro-ruggedness and a large surface area is obtainable. The electrostatic exchange in the stage of development is thus accelerated and stable developing property is obtd. Since the surface area is large, the toner is susceptible to the effect of heat and pressure and good fixability is obtd. in a heat fixing process and pressure fixing process.

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、静電記録、静電印刷に於ける電気的
潜像を現像する乾式トナーの製造方法に関するものであ
る。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a method for producing a dry toner for developing electrical latent images in electrophotography, electrostatic recording, and electrostatic printing.

(従来技術) I¥?−電潜像の形成法は従来周知であシ、例えば、電
子写真法においては、通常光導電体層を帯電させた後、
原図に基いた光像を照射し、光照射部分の静電荷を減少
又は消滅させて静屯浦像を形成する。次いでこの潜像は
トブーーと呼ばれる現像剤で現像される。同知の如く、
現像法は湿式現像剤を用いる方法と乾式現像剤を用いる
方法に大別され、後者は更にキャリアとトナーの2柚の
粒子を用いる一成分現像法とトナーのみ金剛いる/成分
現像法とに分類される。
(Prior art) I¥? - Methods for forming electrostatic latent images are well known in the art; for example, in electrophotography, after charging a photoconductor layer,
A light image based on the original drawing is irradiated to reduce or eliminate static charges in the light irradiated area to form a Seitunura image. This latent image is then developed with a developer called Toboo. As you know,
Development methods are broadly divided into methods using wet developers and methods using dry developers, and the latter are further classified into one-component development methods that use two particles of carrier and toner, and component development methods that use only toner. be done.

さらに、このような現像法によって現像された画像は、
心安に応じて凪等に転写され、その後加熱によシトナー
を溶融さぜるか又は、溶剤によりトナーの結石樹脂を軟
化させるか、又は、単に圧力によシトナーを変形させる
かして、祇等に定着される。
Furthermore, images developed by such a developing method are
Depending on the safety, the toner is transferred to Nagi etc., and then the toner is melted by heating, the calculus resin of the toner is softened by a solvent, or the toner is simply deformed by pressure. will be established.

これら通常のトナーの現像・定着方式ではいずれにせよ
トナー表面の微小凹凸が多く表面積の大きなトナーの方
が、現俄時の電荷交換性が促進されやすく安定した現像
性を示す。さらに、定着性に関しても、表面積の大きな
トナーの方が、熱、圧力の影響を受けやすく、熱定着方
式、圧力定着方式、いずれの場合においても、定着性は
向」ニする。
In any of these conventional toner development and fixing systems, toners with many microscopic irregularities on the toner surface and a large surface area tend to promote charge exchange during development and exhibit stable developability. Furthermore, in terms of fixability, toners with a larger surface area are more susceptible to the effects of heat and pressure, and the fixability is better regardless of whether it is a heat fixing method or a pressure fixing method.

表面の微小凹凸の多いトナーの製法としては、トナー材
料を混線時に発泡させ、以後、粉砕、分級を行なう方法
が考えられる。すなわち、トナー混線時にトナー材料を
発泡させ、トナースラブ中に微ンf州な空間を無数に、
かつ、均一に作シ、それを粉砕することによ、bトナー
粒子表面に制御された微小凹凸構造を形成させるわけで
ある。
As a method for producing a toner having many minute irregularities on the surface, a method can be considered in which the toner material is foamed at the time of cross-crossing, and then pulverized and classified. In other words, when the toner is mixed, the toner material is foamed, creating countless small spaces in the toner slab.
Furthermore, by uniformly producing and pulverizing the particles, a controlled fine uneven structure is formed on the surface of the B toner particles.

トナー混線物を発泡させる方法としては、(h 熱また
は副成分により化学反応を起こしてガスを発生するセ:
:キ剤〔分解型発泡剤:アゾビスホルムアミド、アゾジ
カルボンアミド、ジアゾアミノベンゼン、N、N’−ツ
メチル−N、N’−ジニトロノーテレフタルアミド、N
、N’−ジニトロソペンクメチレンテトラミン、ベンゼ
ンスルホニルヒドラジット、トルエン−(lJQ−スル
ホニル−ヒドラジッド、グ、4t′−オキシビス(ベン
ゼンスルホニル−ヒドラジッド)なト〕ヲ用いる方法: () 機械的に材料を泡立たせて発泡させる方法;(,
71高圧下において不活性ガス(例えばペンタン、ヘキ
サンなど)を材料に吸収させ、常圧で発泡させる方法: などがあるが、(ハの分解型発泡剤を用いる方法では、
発泡剤自身にアミン基、スルホニル基なトノ官能基が含
まれており、未分解で、トナー混線物中に残存した場合
に、トナーの電気特性に、多大な影響を与えることが考
えられ、トナー製造に用いるには、トナー特性の制御と
いった面から不適 )である。また、(、,21の機械
的に発泡させる方法は、トナー?ll!、練物のように
705ポアズを越すような高粘度の物質の場合には、設
備上不適である。(jの高圧下にて不活性ガスを吸収さ
せて常圧で発泡させる方法は、(1)〜(ωの中では、
最も有効と思われるが、加圧4J tipの導入、加圧
条件の設定等、多くの問題を抱えることになる。
The method of foaming the toner mixture is (h) a method in which gas is generated by causing a chemical reaction with heat or subcomponents:
: Key agent [degradable blowing agent: azobisformamide, azodicarbonamide, diazoaminobenzene, N,N'-tumethyl-N,N'-dinitronoterephthalamide, N
, N'-dinitrosopencumethylenetetramine, benzenesulfonylhydrazide, toluene-(lJQ-sulfonyl-hydrazide, 4t'-oxybis(benzenesulfonyl-hydrazide)) Method: () Mechanically converting the material How to foam and foam; (,
71 A method of absorbing an inert gas (e.g. pentane, hexane, etc.) into a material under high pressure and foaming it at normal pressure.
The blowing agent itself contains tono-functional groups such as amine groups and sulfonyl groups, and if it remains undecomposed and remains in the toner mixture, it is thought that it will have a significant impact on the electrical properties of the toner. It is unsuitable for use in manufacturing due to the control of toner properties. In addition, the mechanical foaming method of (,,21) is unsuitable for equipment reasons in the case of highly viscous substances exceeding 705 poise, such as toner?ll! or kneaded materials. The method of absorbing inert gas and foaming at normal pressure is (1) to (ω,
Although this seems to be the most effective method, it poses many problems, such as the introduction of a pressurizing 4J tip and setting of pressurizing conditions.

し〆ζがって現在最も簡1更かつ有効と考えられる方法
は、溶剤型発泡剤をトナー混線物中に、均一に分散させ
て、混練中に生じる熱によって発泡させ、発泡性のトナ
ー混線物を得る方法である。
Therefore, the method currently considered to be the simplest and most effective is to uniformly disperse a solvent-based foaming agent in the toner mixture and foam it with the heat generated during kneading. It's a way of getting things.

溶剤型発泡剤を用いる方法としては、 (a)トナー原材料に溶剤型発泡剤をそのまま混ぜて混
線する方法; (b)トナー原材料に溶剤型発泡剤を含f・”狐もしく
は吸尤させて混線する方法; (C)トナー原材料に、マイクロカプセル化した溶剤型
発泡剤を混ぜて混線する方法: が考えられる。
Methods of using a solvent-based blowing agent include: (a) Mixing the solvent-based blowing agent directly into the toner raw material and mixing it; (b) Mixing the solvent-based foaming agent with the toner raw material and causing it to absorb. Possible methods include: (C) A method of mixing a microencapsulated solvent-based foaming agent with toner raw materials for crosstalk.

ここで、(a)、(b)の方法では、溶剤型発泡剤をト
ナー混線物中に均一に分散させることが困〃准であり、
(c)のマイクロカプセル化した溶剤型発泡剤を用いる
のが最も適した方法と言える。
Here, in the methods (a) and (b), it is difficult to uniformly disperse the solvent-based blowing agent in the toner mixture;
The most suitable method is to use a microencapsulated solvent-based blowing agent (c).

(発明の目的) 従って本発明の目的は、トナー混線物中に微細な空間を
均、−に分散させることにより、トナーの粉砕性を向上
させ、製造性に富むトナーを提供することである。
(Object of the Invention) Accordingly, an object of the present invention is to provide a toner that improves the pulverizability of the toner and is highly manufacturable by evenly dispersing fine spaces in the toner mixture.

本発明の他の目的は、電荷交換性が優れ、極めて安定し
た現像転写性を示すトナーを提供することである。
Another object of the present invention is to provide a toner that has excellent charge exchange properties and exhibits extremely stable development and transfer properties.

更に、本発明の他の目的は、トナー粒子表面に制御され
た微小凹凸構造を形成させることにより、熱定着におい
ても、圧力定着においても定着性の良好なトナーを提供
することである1、(発明の構成) 、本発明者等は鋭意検討の結果結着樹脂、着色剤、その
他添加剤等のトナー原材料に、マイクロカプセル化した
発泡剤、特に溶剤型発泡剤を添加し、混線することによ
り前述の目的が達成されることを見出し本発明を完成し
た。
Furthermore, another object of the present invention is to provide a toner that has good fixability in both heat fixing and pressure fixing by forming a controlled fine uneven structure on the surface of the toner particles. As a result of intensive studies, the present inventors added a microencapsulated foaming agent, particularly a solvent-based foaming agent, to toner raw materials such as a binder resin, colorant, and other additives, and by mixing them. The present invention has been completed by finding that the above object can be achieved.

以下、誉発明の構成を詳細に説明する。The configuration of the honor invention will be explained in detail below.

本発明のトナー結着樹脂としては従来からトナーの粘着
剤として用込られている材料が使用可能でちる1、 例えば、ポリスチレン、ポリ−p−クロルスチレン、ポ
リビニルトルエンなどのスチレン及びそ(7)Ka 体
の一単重合体、スチレン−p−クロルスチレン共ni合
体、スチレン−プロピレン共m合体、スチレン−ビニル
トルエン共重合体、スチレン−ビニルナフタリン共重合
体、スチレン−アクリル酸エステル共重合体、スチレン
−メタクリル酸エステル共重合体、スナレンーαクロル
メタクリルj貨メチル共重合体、スチレン−アクリロニ
トリル共重合体、スチレン−ビニルメチルエーテル共重
合体、スチレン−ビニルエチルエーテル共M 合体、ス
チレン−ビニルメチルケトン共重合体、スチレン−ブタ
ツエン共重合体、スチレンーインゾレン共43合体、ス
チレン−アクリロニトリル−インデン共重合体などのス
チレン系共重合体、ポリ塩化ビニル、天然樹脂変性フェ
ノール、天然便脂変性マレイン戯樹脂、アクリル樹脂、
ポリ酢酸ビニール、シリコーン樹脂、ポリエチレン、ポ
リゾロピレン、ポリエステル414 脂、ポリウレタン
、ポリアミド樹脂、アイオノマー樹脂、7ラン樹脂、工
yJ9キシ樹脂、7キシレン樹脂、ポリビニルブチラー
ル、テルペン樹脂、クマロンインデン樹脂、石油系樹脂
、塩素化パラフィン、パラフィンワックスなどが使用で
きるっ 次に本発明のトナーに用いられる着色剤は従来から静電
宿像現像用トナーに用いられる染料、顔q5Fを用いれ
ばよいが荷電制御剤なども勿論使用できる。また磁性ト
ナーを得たい場合にはマグネタイトなどの磁性微粉末を
混合すればよい。
As the toner binder resin of the present invention, materials conventionally used as adhesives for toners can be used.1 For example, styrene such as polystyrene, poly-p-chlorostyrene, polyvinyltoluene, etc. monopolymer of Ka body, styrene-p-chlorostyrene co-ni polymer, styrene-propylene co-m polymer, styrene-vinyltoluene copolymer, styrene-vinylnaphthalene copolymer, styrene-acrylic acid ester copolymer, Styrene-methacrylic acid ester copolymer, Sunalene-alpha chloromethacrylic methyl copolymer, Styrene-acrylonitrile copolymer, Styrene-vinyl methyl ether copolymer, Styrene-vinyl ethyl ether copolymer, Styrene-vinyl methyl ketone Copolymers, styrene copolymers such as styrene-butatsuene copolymer, styrene-inzolene copolymer, styrene-acrylonitrile-indene copolymer, polyvinyl chloride, natural resin-modified phenol, natural fecal fat-modified malein Play resin, acrylic resin,
Polyvinyl acetate, silicone resin, polyethylene, polyzolopyrene, polyester 414 resin, polyurethane, polyamide resin, ionomer resin, 7 run resin, yJ9 xy resin, 7 xylene resin, polyvinyl butyral, terpene resin, coumaron indene resin, petroleum resin , chlorinated paraffin, paraffin wax, etc. can be used.The coloring agent used in the toner of the present invention may be dyes conventionally used in toners for electrostatic image development, such as q5F, but charge control agents and the like may also be used. Of course you can use it. Further, if it is desired to obtain a magnetic toner, a magnetic fine powder such as magnetite may be mixed.

その他、必要に応じて界面活性剤、酸化防止剤、有(ス
υハ(機充填剤等を添加しても良い。
In addition, surfactants, antioxidants, organic fillers, etc. may be added as necessary.

本発明に使用されるマイクロカプセル化した発泡剤とは
、溶剤型発泡剤を芯剤とし、この外壁に天然又は合成樹
脂を破Φさせたものを示す。ここT、 *lW[!5b
f@l?H: 1.lld、、 ’A400〜“1 )
熱的に安定で化学的に不活性かつ、蒸発速度が犬きく比
熱と蒸発潜熱が小さいものが望丑しい。
The microencapsulated foaming agent used in the present invention refers to one in which a solvent-based foaming agent is used as a core material, and the outer wall of the foaming agent is made of a natural or synthetic resin. Here T, *lW[! 5b
f@l? H: 1. lld,, 'A400 ~ "1)
It is desirable that the material be thermally stable, chemically inert, and have a high evaporation rate and a low specific heat and latent heat of vaporization.

従来、点字コピー、立体根方等を目的として、加メ、・
へ定唐時Cて高τ賞で分u’l 、もしくは蒸発する発
泡剤をトナー中V′c混入するといった試みはあるが、
本発明とは目的・ネ11成において全く異なるものであ
る。
Conventionally, for the purpose of Braille copying, 3D rooting, etc.,
There have been attempts to add V′c to the toner, or to mix evaporating foaming agents into the toner.
This invention is completely different in purpose and structure from the present invention.

また、溶剤型発泡剤の沸点は、マイクロカプセル化した
時の安定性を考r、、゛j、して、Sり℃〜700℃の
6・h囲にあることが望ましい。
Further, the boiling point of the solvent-based blowing agent is desirably within the 6.h range of 700°C to 700°C, taking into consideration the stability when microencapsulated.

例えば、一般的にはゼラチンーアラビアコゞム水浴液に
ヘキサン又はイソヘキサン又は、イソへブタン又はヘプ
タン等の溶剤型発泡剤を懸6、コシ、コアセルベーショ
ン法によって内部に溶剤量−#、泡剤?!−汀むマイク
ロカフ0セルを作ることが可能である。
For example, in general, a solvent-based foaming agent such as hexane, isohexane, isohbutane or heptane is suspended in a gelatin-Arabic water bath solution, and the amount of solvent is added to the inside by the coacervation method. Agent? ! - It is possible to create microcuff zero cells that stagnate.

寸だ、他の一役的な方法として、ヘキサメチレンビスク
ロロホルメートのベンゼン?8 +11 ヲ水中テ乳化
し、これにヘギサメチレンソアミンを加え、昇向屯縮合
法により、内部に訂剤型発泡剤を含むマイクロカプセル
を作ることかり能である。
Okay, another possible method is to use benzene in hexamethylene bischloroformate? 8 + 11 It is possible to emulsify the emulsified product in water, add hegisamethylenesoamine to the emulsified product, and use the shogoton condensation method to produce microcapsules containing a foaming agent inside.

さらに別の方法としては、(°1脂澗畝に溶剤型発泡剤
をR’4i 1iTlさぜ、スフ0レードライ法で樹脂
溶媒を蒸発させることによって内部に溶剤型発泡剤を含
むマイクロカプセルを作ること等が可能である。
Yet another method is to create microcapsules containing a solvent-based foaming agent inside by adding a solvent-based foaming agent to R'4i 1iTl in the R'4i 1iTl layer and evaporating the resin solvent using the spray drying method. This is possible.

このようにして得られたマイクロカプセル化物は結着樹
脂、着色剤、その他添加剤等のトナー原材料に添加され
、混練される。
The microcapsules thus obtained are added to toner raw materials such as a binder resin, a colorant, and other additives, and then kneaded.

況合比については、溶剤型発泡剤量が、トナー結オイ剤
/θ0屯置部に対し0.7〜15、好ましくは7〜70
部が良い。0.7部以下では発泡効果が小さく、また/
左部以上でit発泡剤を完全に発泡させるのに時間を要
し、混線中にトナー材料が熱により変質する可能性もあ
るので好ましくない、(実施例) 以下、実施例について説明する。
Regarding the situation ratio, the amount of the solvent-based blowing agent is 0.7 to 15, preferably 7 to 70, relative to the toner oil binding agent/θ0 ton placement part.
The department is good. If it is less than 0.7 parts, the foaming effect will be small, and /
It takes time to completely foam the IT foaming agent above the left side, and the toner material may be deteriorated by heat during cross-talk, which is not preferable. (Example) Examples will be described below.

「部」、1%」は屯ト]士部、厩量%を示す。``Part'', 1%'' indicates the amount of stable space %.

比較し1」トナーA スチレン−n−ブチルメタクリレート共重合体(型骨平
均分子量約Sθ、000) 22部、スチレン県架SI
Bポリマー、23部、低分子1Ltポリグロビレンワツ
クス(重量乎均分子景グθθ0)5部、四三酸化鉄(粒
状、平均粒径θ、5μ)30部を溶融、混綜し、その後
粉砕を行なったが、粉砕性が悪く平均粒径/ g /Z
 程度にしか粉砕出来なかった。これをさらに分級して
平均粒径/Sμの磁性トナーを倚た1 こうして得だトナーにカーボンブラック(平均粒径0.
θλμ)を0.3%加え、高速で回転する(n拌羽根を
有する費拌装置)1で攪拌を行ない、トナー粒子状面に
カーフJ!ンブラックを付着させたトナーA 4:イq
プヒ。
Comparison 1" Toner A Styrene-n-butyl methacrylate copolymer (type bone average molecular weight approximately Sθ, 000) 22 parts, Styrene Kenka SI
23 parts of B polymer, 5 parts of low molecular weight 1Lt polyglobylene wax (weight and average molecular size θθ0), and 30 parts of triiron tetroxide (granular, average particle size θ, 5μ) were melted and mixed, and then Although pulverization was performed, the pulverization properties were poor and the average particle size/g/Z
I could only crush it to a certain extent. This was further classified to obtain a magnetic toner with an average particle size of /Sμ.1 The thus obtained toner contained carbon black (average particle size of 0.
0.3% of θλμ) was added and stirred with a high-speed rotating device (a stirring device with n stirring blades) 1 to form a kerf J! on the surface of the toner particles. Toner A with black attached 4: Iq
Puhi.

トナーAを用い−C富士ゼロックス(株) 娯F X−
2g30に/成分・fH影成を111込んだ葆写俵でコ
ピーをとったところ、垣初の/θコピー位は画像6′4
度が出なかった。10コピー以後は一応安定した濃度の
画像が得られたが、反射し度=/、/とやや低目であっ
た。また定后温度をK”1べたところ770℃で一応艮
好な定;τiレベルが得られた。
Using toner A-C Fuji Xerox Co., Ltd. Entertainment FX-
When I made a copy using 2g30 with 111 /components/fH shadows, the /θ copy position of Kaki's first image was 6'4
I was out of control. After the 10th copy, an image with a somewhat stable density was obtained, but the degree of reflection was a little low at /, /. Further, when the temperature after constant temperature was determined by K''1, a reasonably good constant; τi level was obtained at 770°C.

シこPL 例 / ト ナー B トナーAと傘く同じ桜類、Mの原拐料に、カプセル化し
た溶剤フL11発泡剤を、芯剤に換算して、乙部加えて
γt’r !1.”Aび1、蘇し、イ1」は比軟a゛す
と全く同様にしてトナーBを得た。
Shiko PL Example / Toner B Toner B, which is the same as Toner A, add the encapsulated solvent L11 foaming agent to the core material and add Otobe to the M base material, and add γt'r! 1. Toner B was obtained in exactly the same manner as "Abi1, Revival, A1".

カプセル化した溶剤型発泡剤の芯剤として、n−へキサ
ン全用いた。丑ず、n−ヘキサンにヘキサメチレン・ビ
スクロロホルメートを溶解しり液全水中に分散させて、
高速硯拌して乳化させた。これにヘキサメチレンツアミ
ン水浴液を加え、界面1【合法によシ、平均粒径10μ
mのn−ヘキサン會Mポリウレタン壁マイクロカプセル
を得だ。
n-hexane was used as the core agent for the encapsulated solvent-based blowing agent. Dissolve hexamethylene bischloroformate in n-hexane and disperse it in the whole water of the periwinkle liquid.
It was emulsified by high-speed stirring. Add hexamethylenezamine water bath solution to this, and interface 1 [legal, average particle size 10μ]
Polyurethane-walled microcapsules were obtained using n-hexane.

カプセル化した発泡剤全加え−C混練を行なった。All of the encapsulated blowing agent was added and kneading was carried out.

トナーBのスラブには無数の気泡がall Bされた。Numerous air bubbles were formed in the toner B slab.

トナーBe1−ナーAと同−灸件のもとで粉砕すると、
トナーBの粉砕性はトナー八より優れ、平均粒径/、2
μmのトナーが得られた。
Toner Be1 - When crushed under the same moxibustion conditions as Toner A,
The crushability of Toner B is superior to Toner 8, with an average particle size of /,2
A .mu.m toner was obtained.

また、トナーAと全く同じ方法でコピーB・ト価を行な
ったところ/コピー目から安定した濃度(lD−/、3
) の画像が得られた。まだ定着温度は15り℃で満足
のゆく別府画像強度が得られた。
In addition, when copy B was tested in the same manner as toner A, the density was stable from the first copy (lD-/, 3
) images were obtained. Satisfactory Beppu image strength was still obtained at a fixing temperature of 15°C.

“f B OJ) gt (#″22″・”′17“”
d−Aj、9゜改善された原因については、発泡剤を入
れることにより、トナースラブが多孔屓となシ、該スラ
ブを粉砕することで、表面積の大きなトナーとなった7
Yめと推定される。
"f B OJ) gt (#"22"・"'17""
d-Aj, 9° The reason for the improvement is that by adding a foaming agent, the toner slab becomes porous, and by crushing the slab, a toner with a large surface area is created.7
It is estimated that she is Y-ish.

トナーBが微小凹凸に富む形状をもっていること(l′
i追3(y−q及び走−1!f塑電子顕微蜘で4+7i
i認を行なった。っ 爽a 例 、2 ト す − C 月?リスチレン樽脂、23部、低分子IXセポリエチレ
ンワックス72部、スチレン−ブタジェン共重合体S都
、四三p化鎌乙0部をトナー材料として秤jN、’ し
た。
Toner B has a shape rich in minute irregularities (l'
i added 3 (y-q and run-1!f plastic electron microscope spider 4+7i
I conducted an i-certification. ssou a example, 2 toss - C month? 23 parts of listyrene barrel fat, 72 parts of low-molecular IX sepolyethylene wax, styrene-butadiene copolymer S, and 0 parts of 43-p compound were weighed out as toner materials.

一方、コアセルベーション法によす、芯物亘にn−ヘキ
サン受用い、外Fをゼラチン−′rラビアゴムで被0′
之したSト均わ14径/夕μmのマイクロカプセルを作
成し、Ji−6 上1己トナー材4斗にマイクロカシセルを、n−ヘキサ
ンに換算して7部混合した後に溶融扉練し、比截例と同
一・の方法で粉砕を行なったところ、平均粒径/3μm
のトナーが得られた。このトナーを用いてトナー八と全
く同じ方法でコピー評価を1i々つ/こところ、/コピ
ー目から安ンと′した画1祝♂1度(印−/、3)が得
られた。さらにこの画像をhQ圧λθFf/ca が印
加されたローラー間を通して定着を行なったところ、7
11足のゆく定着像強度が得られた。・ 実施例3 トナーD スチレン−n−ブチルメタクリレート共AfK(、@ 
’in平均分子量力60.θθθ)gり部、低分子量ン
15すプロlJ″Vンワックス(重介平均分子Jd、グ
、θ0θ)5部、カーボンブラック10部に、実施例/
で用いたカプセル化した溶剤型発泡剤を芯剤に換算して
70部加え、溶融混錬をした後、粉砕、分級を行ない平
均粒径/3μのトナーを得た。ついでこのトナー2部を
鉄粉(粒径/θθμ)100部と混合して現像剤とし/
こっこの現像剤を用いて市販のFx−,2g、30を用
いてコピー評il′ltIを行なったところ、+i!i
i 1:#濃度は1戊目(ID−/、、2 ) であシ
、十分酒足のゆくコピーが得らJ′Lだ。定りΔ温度を
調べると、770℃で満足のゆく定着俳弘度がイーけら
れた。
On the other hand, according to the coacervation method, n-hexane was applied over the core material, and the outer F was coated with gelatin-'r rubia rubber.
Microcapsules with a uniform diameter of 14 μm were prepared, and 4 parts of Ji-6 toner material were mixed with 7 parts of microcassicle (calculated as n-hexane), and then kneaded with a melting door. When pulverization was carried out in the same manner as in the comparative example, the average particle size/3μm
of toner was obtained. Using this toner, copy evaluation was performed in exactly the same manner as toner 8, and a score of 1/1/3 was obtained with a safe score of 1/1/3. Furthermore, when this image was fixed by passing it between rollers to which hQ pressure λθFf/ca was applied, 7
A fixed image intensity of 11 points was obtained. - Example 3 Toner D Styrene-n-butyl methacrylate co-AfK (,@
'in average molecular weight force 60. Examples/
70 parts of the encapsulated solvent-type foaming agent used in the above was added in terms of core material, and after melting and kneading, the mixture was pulverized and classified to obtain a toner having an average particle size of 3 μm. Next, 2 parts of this toner was mixed with 100 parts of iron powder (particle size/θθμ) to form a developer.
When I performed a copy evaluation using commercially available Fx-, 2g, and 30 using this developer, +i! i
i 1:# The density is 1st (ID-/,, 2), so if you get a copy that you can drink enough, it's J'L. When the fixed Δ temperature was examined, a satisfactory fixing efficiency was achieved at 770°C.

Claims (1)

【特許請求の範囲】[Claims] (1)結着樹脂、着色剤、その他添加剤等のトナー原材
料にマイクロカプセル化した発泡剤を添加し、混ii’
j!3すると七を11“ケ徴とするトナー製造方法。
(1) Microencapsulated foaming agents are added to toner raw materials such as binder resins, colorants, and other additives, and mixed with
j! 3. A toner manufacturing method that uses 7 as an 11" character.
JP58112221A 1983-06-22 1983-06-22 Production of toner Pending JPS603646A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58112221A JPS603646A (en) 1983-06-22 1983-06-22 Production of toner

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58112221A JPS603646A (en) 1983-06-22 1983-06-22 Production of toner

Publications (1)

Publication Number Publication Date
JPS603646A true JPS603646A (en) 1985-01-10

Family

ID=14581280

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58112221A Pending JPS603646A (en) 1983-06-22 1983-06-22 Production of toner

Country Status (1)

Country Link
JP (1) JPS603646A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001134006A (en) * 1999-11-01 2001-05-18 Fuji Xerox Co Ltd Image forming device
JP2003084491A (en) * 2001-09-11 2003-03-19 Ricoh Co Ltd Method of evaluating electrophotographic toner, electrophotographic toner, two-component type developer and method of manufacturing electrophotographic toner
US20130011782A1 (en) * 2010-03-17 2013-01-10 Tp,Pegawa Co., Ltd Polymer expanded particle, expanded toner and method for producing polymer expanded particle and expanded toner

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001134006A (en) * 1999-11-01 2001-05-18 Fuji Xerox Co Ltd Image forming device
JP2003084491A (en) * 2001-09-11 2003-03-19 Ricoh Co Ltd Method of evaluating electrophotographic toner, electrophotographic toner, two-component type developer and method of manufacturing electrophotographic toner
JP4602612B2 (en) * 2001-09-11 2010-12-22 株式会社リコー Method for evaluating electrophotographic toner, electrophotographic toner, two-component developer, and method for producing electrophotographic toner
US20130011782A1 (en) * 2010-03-17 2013-01-10 Tp,Pegawa Co., Ltd Polymer expanded particle, expanded toner and method for producing polymer expanded particle and expanded toner

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