JPH01101557A - Toner for developing electrostatic charge image - Google Patents
Toner for developing electrostatic charge imageInfo
- Publication number
- JPH01101557A JPH01101557A JP62258716A JP25871687A JPH01101557A JP H01101557 A JPH01101557 A JP H01101557A JP 62258716 A JP62258716 A JP 62258716A JP 25871687 A JP25871687 A JP 25871687A JP H01101557 A JPH01101557 A JP H01101557A
- Authority
- JP
- Japan
- Prior art keywords
- toner
- particles
- fine
- sleeve
- toner particles
- 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
Links
- 239000002245 particle Substances 0.000 claims abstract description 73
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 33
- 239000011347 resin Substances 0.000 claims abstract description 21
- 229920005989 resin Polymers 0.000 claims abstract description 21
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 12
- 230000002209 hydrophobic effect Effects 0.000 claims abstract description 8
- 239000003086 colorant Substances 0.000 claims abstract description 6
- 239000011230 binding agent Substances 0.000 claims abstract description 5
- 239000006249 magnetic particle Substances 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 26
- 239000003795 chemical substances by application Substances 0.000 abstract description 9
- 239000010419 fine particle Substances 0.000 abstract description 9
- 238000005498 polishing Methods 0.000 abstract description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 8
- 108091008695 photoreceptors Proteins 0.000 description 7
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 7
- 239000004926 polymethyl methacrylate Substances 0.000 description 7
- 239000000843 powder Substances 0.000 description 7
- 239000008119 colloidal silica Substances 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 5
- 239000000919 ceramic Substances 0.000 description 5
- 230000007423 decrease Effects 0.000 description 5
- 239000000975 dye Substances 0.000 description 5
- -1 Hansa Yellow Chemical compound 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000000945 filler Substances 0.000 description 3
- 239000006247 magnetic powder Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 229910002012 Aerosil® Inorganic materials 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 229920006243 acrylic copolymer Polymers 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- FFUAGWLWBBFQJT-UHFFFAOYSA-N hexamethyldisilazane Chemical compound C[Si](C)(C)N[Si](C)(C)C FFUAGWLWBBFQJT-UHFFFAOYSA-N 0.000 description 2
- 230000009191 jumping Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 238000007639 printing Methods 0.000 description 2
- 238000010298 pulverizing process Methods 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- FWLHAQYOFMQTHQ-UHFFFAOYSA-N 2-N-[8-[[8-(4-aminoanilino)-10-phenylphenazin-10-ium-2-yl]amino]-10-phenylphenazin-10-ium-2-yl]-8-N,10-diphenylphenazin-10-ium-2,8-diamine hydroxy-oxido-dioxochromium Chemical compound O[Cr]([O-])(=O)=O.O[Cr]([O-])(=O)=O.O[Cr]([O-])(=O)=O.Nc1ccc(Nc2ccc3nc4ccc(Nc5ccc6nc7ccc(Nc8ccc9nc%10ccc(Nc%11ccccc%11)cc%10[n+](-c%10ccccc%10)c9c8)cc7[n+](-c7ccccc7)c6c5)cc4[n+](-c4ccccc4)c3c2)cc1 FWLHAQYOFMQTHQ-UHFFFAOYSA-N 0.000 description 1
- AXDJCCTWPBKUKL-UHFFFAOYSA-N 4-[(4-aminophenyl)-(4-imino-3-methylcyclohexa-2,5-dien-1-ylidene)methyl]aniline;hydron;chloride Chemical compound Cl.C1=CC(=N)C(C)=CC1=C(C=1C=CC(N)=CC=1)C1=CC=C(N)C=C1 AXDJCCTWPBKUKL-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
- 235000010919 Copernicia prunifera Nutrition 0.000 description 1
- 244000180278 Copernicia prunifera Species 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- 229910052576 carbides based ceramic Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000007667 floating Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 1
- MOUPNEIJQCETIW-UHFFFAOYSA-N lead chromate Chemical compound [Pb+2].[O-][Cr]([O-])(=O)=O MOUPNEIJQCETIW-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000696 magnetic material Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000011812 mixed powder Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000767 polyaniline Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- KAKZBPTYRLMSJV-UHFFFAOYSA-N vinyl-ethylene Natural products C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- XOSXWYQMOYSSKB-LDKJGXKFSA-L water blue Chemical compound CC1=CC(/C(\C(C=C2)=CC=C2NC(C=C2)=CC=C2S([O-])(=O)=O)=C(\C=C2)/C=C/C\2=N\C(C=C2)=CC=C2S([O-])(=O)=O)=CC(S(O)(=O)=O)=C1N.[Na+].[Na+] XOSXWYQMOYSSKB-LDKJGXKFSA-L 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/097—Plasticisers; Charge controlling agents
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Developing Agents For Electrophotography (AREA)
Abstract
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、静電印刷法等において静電荷像
を現像するのに用いられるトナー社係り、特に1成分系
の非磁性トナーに関する。Detailed Description of the Invention [Field of Industrial Application] The present invention relates to toners used to develop electrostatic images in electrophotography, electrostatic printing, etc., and particularly to one-component nonmagnetic toners. Regarding.
電子写真法、静電印刷法等においては、種々の手段によ
り感光体の表面に静電荷像を形成し、この静電荷像をト
ナーにより現像し、現像により得られたトナー像を普通
紙等に転写した後定着し、最終画像を得るのが一般的で
ある。In electrophotography, electrostatic printing, etc., an electrostatic charge image is formed on the surface of a photoreceptor by various means, this electrostatic charge image is developed with toner, and the developed toner image is printed on plain paper, etc. Generally, the image is transferred and then fixed to obtain the final image.
静電荷像を現像する方法としては、磁気ブラシ法が一般
的であり、この磁気ブラシ法には、鉄粉またはフェライ
ト粉末などのキャリアと樹脂着色剤を主体とするトナー
との混合粉体である2成分系曳像剤が従来から多用され
ている。2成分系現像剤を使用する場合の欠点としては
、トナーとキャリアとの混合比(トナー濃度)を厳密に
制御しないと画質が安定しないので、トナー濃度の制御
手段が必要となることおよび長時間の使用においてキャ
リアの表面がトナーで汚染され、キャリアの摩擦帯電能
力が低下すること等が挙げられる。A common method for developing electrostatic images is the magnetic brush method, which uses a mixed powder of a carrier such as iron powder or ferrite powder and a toner mainly containing a resin colorant. Two-component repellents have been widely used. The disadvantages of using a two-component developer are that the image quality is unstable unless the mixing ratio of toner and carrier (toner concentration) is strictly controlled, so a means of controlling the toner concentration is required, and it can be used for a long time. When using the carrier, the surface of the carrier becomes contaminated with toner, and the triboelectric charging ability of the carrier decreases.
このような欠点を解消するために、樹脂と磁性粉を主体
とする磁性トナーを用いる1成分現像法が開発され、実
用化されている。1成分現像法においては、良好な転写
性を得るために絶縁性磁性トナーを用いる(例えば特開
昭53−31136号参照)ことが多い。現像方法につ
いても種々の方法が提案されているが、トナー相互の摩
擦、トナーとスリーブ等との摩擦によりトナーを摩擦帯
電させる方法が多用されている。In order to overcome these drawbacks, a one-component developing method using a magnetic toner mainly composed of resin and magnetic powder has been developed and put into practical use. In the one-component development method, an insulating magnetic toner is often used to obtain good transferability (see, for example, Japanese Patent Laid-Open No. 31136/1983). Although various developing methods have been proposed, a method in which the toner is triboelectrically charged by friction between the toners or between the toner and a sleeve or the like is often used.
しかしトナーの摩擦帯電を利用した現像法では、トナー
が凝集し易くなるおよび環境条件により画質が変化し易
いという欠点がある。また磁性トナーはマグネタイト等
の磁性粉を20〜70重量%程度含むので、2成分系現
像剤よりも定着性が劣るという欠点がある。However, the developing method using triboelectric charging of toner has drawbacks in that the toner tends to aggregate and the image quality tends to change depending on environmental conditions. Further, since magnetic toner contains about 20 to 70% by weight of magnetic powder such as magnetite, it has a disadvantage that it has poorer fixing properties than two-component developers.
このようなことから、磁性粉を含有しない非磁性1成分
トナーを用いる現像法が注目されている。For these reasons, a developing method using a non-magnetic one-component toner that does not contain magnetic powder is attracting attention.
非磁性1成分現像法としては、インプレッション現像法
、タッチダウン現像法あるいはジャンピング現像法がよ
く知られている。しかしながらインプレッション現像法
およびタッチダウン現像法では、トナー担持体と感光体
とが接触するので、カプリが生じてしまう。またジャン
ピング現像法では、現像効率を上げるためにトナー担持
0体と感光体との間隙を狭め、この間隙にトナーの薄層
を係結する必要があるが、均一な厚さのトナーの薄層を
形成することが困難である。As the nonmagnetic one-component development method, an impression development method, a touchdown development method, or a jumping development method is well known. However, in the impression development method and the touchdown development method, since the toner carrier and the photoreceptor come into contact with each other, caps occur. In addition, in the jumping development method, in order to increase development efficiency, it is necessary to narrow the gap between the toner-carrying body and the photoreceptor, and to bind a thin layer of toner in this gap. difficult to form.
そこでこれらの欠点を除くために、トナー担持体として
表面に複数個の浮遊電極を備えたスリーブを用いること
が検討されている。第1図および第2図に示される如く
、スリーブ1は、アルミニウム、ステンレス鋼等の非磁
性かつ導電性材料からなる基体2上に、誘電性層3を形
成し、誘電性層3の表面に微小電極4となる多数の誘電
性粒子を相互に電気絶縁状態に保持した構造を有してい
る。このような構造のスリーブは、例えば特開昭60−
225179号に開示されている。第1図の装置によれ
ば、容器5内に収容されたトナー8を図示しない適当な
手段で摩擦帯電させながらスリーブlを回転させ、回転
と共に、スリーブとトナー層の厚みを規制するためのド
クタ一部材6との間にバイアス電圧源7を接続し、両者
間にバイアス電圧を印加させることにより、感光体10
の表面に形成された静電荷像(図示せず)の現像が行な
われる。この現像法によれば、十分なエッヂ効果を安定
して発揮できるので、面画像および線画像ともに良好゛
な画像を得ることができる。Therefore, in order to eliminate these drawbacks, it has been considered to use a sleeve having a plurality of floating electrodes on its surface as a toner carrier. As shown in FIGS. 1 and 2, the sleeve 1 includes a dielectric layer 3 formed on a base 2 made of a non-magnetic and conductive material such as aluminum or stainless steel, and a dielectric layer 3 formed on the surface of the dielectric layer 3. It has a structure in which a large number of dielectric particles forming the microelectrodes 4 are kept electrically insulated from each other. A sleeve having such a structure is disclosed in, for example, Japanese Patent Application Laid-Open No. 1986-
No. 225179. According to the apparatus shown in FIG. 1, the sleeve l is rotated while the toner 8 housed in the container 5 is triboelectrically charged by an appropriate means (not shown), and along with the rotation, a doctor is used to regulate the thickness of the sleeve and the toner layer. By connecting a bias voltage source 7 between one member 6 and applying a bias voltage between the two, the photoreceptor 10
An electrostatic charge image (not shown) formed on the surface is developed. According to this developing method, it is possible to stably exhibit a sufficient edge effect, so that it is possible to obtain both good surface images and line images.
上述した非磁性1成分系トナーは、結着樹脂と着色剤と
を主体として構成されているので、長期間の使用におい
てトナーが現像ロール(例えば微小電極付スリーブ)の
表面に付着してトナーの薄層を形成することになる。そ
の結果スリーブにバイアス電圧を印加しても微小電極と
感光体との間の電界強度が低下し、画像濃度が低下する
という問題が生ずる。The above-mentioned non-magnetic one-component toner is mainly composed of a binder resin and a colorant, so when used for a long period of time, the toner adheres to the surface of the developing roll (for example, a sleeve with a microelectrode), causing the toner to deteriorate. A thin layer will be formed. As a result, even if a bias voltage is applied to the sleeve, the electric field strength between the microelectrode and the photoreceptor decreases, resulting in a problem that the image density decreases.
したがって本発明の目的は、非磁性1成分現像法に適用
して多数枚の複写を行なっても良好な画像が得られる静
電荷像現像用トナーを提供することである。Therefore, an object of the present invention is to provide a toner for developing electrostatic images that can be applied to a non-magnetic one-component developing method and that can produce good images even when a large number of copies are made.
c問題点を解決するための手段〕
本発明の静電荷像現像用トナーは、結着樹脂と着色剤と
研摩剤微粒子とを含有する非磁性粒子の表面に疎水性シ
リカと平均粒径1μm以下の樹脂微粒子とを添加したト
ナー粒子からなり、前記トナー粒子は平均粒径が8〜1
0μmの範囲にあり、かつ、粒径20μm以上の粒子は
実質的に含まれていないような粒度分布を有することを
特徴とする。Means for Solving Problems] The toner for developing electrostatic images of the present invention has hydrophobic silica on the surface of nonmagnetic particles containing a binder resin, a colorant, and fine abrasive particles, and an average particle size of 1 μm or less. The toner particles have an average particle size of 8 to 1.
It is characterized by having a particle size distribution in the range of 0 μm and substantially free of particles with a particle size of 20 μm or more.
本発明のトナーは、トナー粒子の内部に研摩剤微粒子を
含有し、この研摩剤微粒子す内トナー粒子の表面に露出
した部分によりスリーブ表面を研摩すると共に、トナー
粒子の表面に添加したシリカ微粉末でスリーブ表面を研
摩することにより、トナーの付着を防止し、更に、トナ
ー粒子の表面に樹脂微粒子を添加することにより流動性
及び定着性の向上を図るものである。The toner of the present invention contains fine abrasive particles inside the toner particles, and the part exposed on the surface of the toner particles inside the fine abrasive particles polishes the sleeve surface, and fine silica powder added to the surface of the toner particles. By polishing the sleeve surface, toner adhesion is prevented, and furthermore, by adding resin fine particles to the surface of the toner particles, fluidity and fixing properties are improved.
本発明を構成する各材料について述べる。Each material constituting the present invention will be described.
結着樹脂としては、例えば、ポリスチレン、スチレン・
ブタジェン共重合体、スチレン・アクリル酸エステル等
のスチレン系樹脂、エポキシ樹脂、ポリエステル樹脂等
の公知のトナー用樹脂を単独又は混合して用いることが
できる。Examples of binder resins include polystyrene, styrene, etc.
Known toner resins such as butadiene copolymers, styrene resins such as styrene/acrylic acid esters, epoxy resins, and polyester resins can be used alone or in combination.
着色剤としては、カーボンブランク、クロムイエロー、
ハンザイエロー、ベンジンイエロー、ローズベンガル、
アニリンレッド、フタロシアニンブルー、アニリンブル
ー、ニグロシン染料、アニリンブラック等の公知の顔料
あるいは染料を用い得る。その添加量は3〜10重景%
重量囲がよい。Colorants include carbon blank, chrome yellow,
Hansa Yellow, Benzine Yellow, Rose Bengal,
Known pigments or dyes such as aniline red, phthalocyanine blue, aniline blue, nigrosine dye, and aniline black can be used. The amount added is 3-10%
Good weight range.
研摩剤微粒子としては、窒化物系または炭化物系セラミ
ックス、及びそれらを混合したセラミックスのような材
料が用い得る。このようなセラミックスとしては、例え
ばB、C5TtC% StC5TiN −。As the abrasive particles, materials such as nitride-based or carbide-based ceramics, and ceramics that are a mixture thereof can be used. Examples of such ceramics include B, C5TtC% StC5TiN -.
5iJaが挙げられる。研摩剤微粒子の大きさは、トナ
ー中に均一に分散せしめ、かつ、ロール表面の損傷を防
ぐために平均粒径で3μm以下とすることが望ましい。5iJa. The size of the abrasive fine particles is desirably 3 μm or less in average particle size in order to ensure uniform dispersion in the toner and to prevent damage to the roll surface.
その添加量は、少ないと効果がなく、多いとスリーブや
感光体等の部材を傷付は易いので、0.5〜3.゛5重
量%の範囲がよく、より好ましくは0.7〜2.0重量
%である。The amount added should be 0.5 to 3. The range is preferably 5% by weight, more preferably 0.7 to 2.0% by weight.
上記のセラミックスは公知の手法によりつくることがで
きる。例えば、水素、窒素の単独又は混合ガス中で発生
させたアークまたはプラズマジェットにより、セラミッ
クスあるいはセラミックスに金属または炭素を混合した
混合物を加熱する方法(特開昭59−227765号参
照)が適用できる。The above ceramics can be made by known methods. For example, a method (see JP-A-59-227765) of heating ceramics or a mixture of ceramics and metal or carbon using an arc or plasma jet generated in hydrogen or nitrogen gas alone or in a mixed gas can be applied.
本発明に係るトナー粒子は、上記の各成分と共に、帯電
制御剤、離型剤、充填剤等の添加物を含有することがで
きる。帯電制御剤としては、ニグロシン染料、ニグロシ
ン染料とカルボキシル基含有樹脂との反応物、トリフェ
ニルメタン系染料、含金属(Cr)アゾ染料など、離型
剤としては、ポリプロピレン、ポリエチレン、パラフィ
ンワックス、カルナバワックス、アミドワックスなど、
充填剤としては炭酸カルシウム、タルク、クレイ等の無
機微粉末などを用い得る。これらの含有量は、トナーに
要求される特性に応じて適宜定められるが、一般に帯電
制御剤が1〜5重景重量離型剤が1〜5重景重量充填剤
が1〜10重量%の範囲が望ましい。The toner particles according to the present invention can contain additives such as a charge control agent, a mold release agent, and a filler in addition to the above-mentioned components. Charge control agents include nigrosine dyes, reaction products of nigrosine dyes and carboxyl group-containing resins, triphenylmethane dyes, metal-containing (Cr) azo dyes, etc. Release agents include polypropylene, polyethylene, paraffin wax, carnauba, etc. wax, amide wax, etc.
As the filler, inorganic fine powder such as calcium carbonate, talc, clay, etc. can be used. These contents are determined as appropriate depending on the characteristics required of the toner, but generally the charge control agent is 1 to 5, the release agent is 1 to 5, and the filler is 1 to 10% by weight. Range is preferred.
次に、上記のトナー粒子の表面には、現像スリーブ表面
へのトナーの付着を防止するために、微粉末シリカを添
加するが、その添加量は、トナー粒そ100重量部当り
0.5〜2重量部の範囲がよい、添加量が0.5重量部
未満では流動性が低下し、スリーブ表面の研摩作用が少
なく、2重量部を越えると定着性が低下するので好まし
くない。この微粒末シリカとしては、市販の疎水性コロ
イダルシリカをそのまま使用してもよいが、トナーの流
動性及び耐湿度安定性の点から疎水性指数が50以上の
もの(特開昭58−81650号)が好ましい。更に平
均粒径が14nm以上の疎水性コロイダルシリカを用い
ると流動性がより向上する。Next, fine powder silica is added to the surface of the above toner particles in order to prevent the toner from adhering to the surface of the developing sleeve, and the amount of addition is 0.5 to 100 parts by weight of the toner particles. The range of 2 parts by weight is preferable; if the amount added is less than 0.5 parts by weight, the fluidity will decrease and the abrasive action on the sleeve surface will be small, and if it exceeds 2 parts by weight, the fixing properties will deteriorate, which is not preferable. As this fine powder silica, commercially available hydrophobic colloidal silica may be used as is, but from the viewpoint of toner fluidity and humidity resistance stability, one with a hydrophobicity index of 50 or more (Japanese Patent Application Laid-open No. 58-81650 ) is preferred. Furthermore, when hydrophobic colloidal silica having an average particle size of 14 nm or more is used, fluidity is further improved.
また、本発明においては、流動性及び定着性を向上する
ためにトナー粒子の表面に樹脂微粒子を添加するが、粒
径が大きすぎるとトナー粒子から離脱し易くなり、画像
を汚すので、平均粒径1μl以下の微粒子とする。その
添加量は、トナー粒子100重量部当り1〜5重量部の
範囲が望ましい。In addition, in the present invention, fine resin particles are added to the surface of the toner particles in order to improve fluidity and fixing properties, but if the particle size is too large, they will easily separate from the toner particles and stain the image. Fine particles with a diameter of 1 μl or less should be used. The amount added is preferably in the range of 1 to 5 parts by weight per 100 parts by weight of toner particles.
添加量が1重量部未満ではその効果がなく、5重量部を
越えると、トナー粒子表面から遊離した余剰の樹脂微粒
子が存在するのでトナーの帯電性が不安定となる。この
ような樹脂微粒子としては、トナーの凝集を防ぐために
50℃以上のガラス転移温度を有するものが好ましい。If the amount added is less than 1 part by weight, there is no effect, and if it exceeds 5 parts by weight, the chargeability of the toner becomes unstable due to the presence of excess resin particles liberated from the surface of the toner particles. Such fine resin particles preferably have a glass transition temperature of 50° C. or higher in order to prevent toner agglomeration.
このような樹脂微粒子を構成する樹脂としては、公知の
熱可塑性樹脂を用い得るが、例えばアクリル系樹脂ある
いはポリメチルメタクリレート、ポリnブチルメタクリ
レート共重合体等のアクリル−ビニル系モノマーの共重
体が挙げられる。As the resin constituting such resin particles, known thermoplastic resins can be used, such as acrylic resins or copolymers of acrylic-vinyl monomers such as polymethyl methacrylate and poly-n-butyl methacrylate copolymers. It will be done.
本発明のトナーは、粉砕法、スプレードライ法等の公知
の手法により製造することができる。粉砕法による場合
は、各原料をボールミル、乾式ミキサー等により予備混
合し、ニーダ、ロールにより加熱混練し、冷却後ジェッ
トミルで粉砕し、次いで分級することによりトナー粒子
を得る。しかる後トナー粒子に疎水性シリカおよび樹脂
微粒子を添加し、これらを混合してトナー粒子表面にこ
れらを保持せしめる。トナーの粒度分布は、画質の点か
ら平均粒径が8〜10μmの範囲にあり、かつ、粒径2
0μm以上の粒子を実質的に含まないように調整すると
よい、これは次のような理由による。平均粒径が8μm
未満であると、流動性が極端に低下し、又トナーが飛散
し易くなり、10μmを越えると印字画像上、文学部周
辺に付着するトナーが目立ち、解像度が低下し、また粒
径20μm以上の粒子が多く含まれていると、白地部の
トナー付着、すなわち地かぶりが目立つためである。The toner of the present invention can be manufactured by a known method such as a pulverization method or a spray drying method. In the case of the pulverization method, the raw materials are premixed using a ball mill, dry mixer, etc., heated and kneaded using a kneader and rolls, cooled, pulverized using a jet mill, and then classified to obtain toner particles. Thereafter, hydrophobic silica and fine resin particles are added to the toner particles and mixed to retain them on the surface of the toner particles. From the viewpoint of image quality, the particle size distribution of the toner is such that the average particle size is in the range of 8 to 10 μm, and the particle size is 2.
It is preferable to adjust the composition so that it does not substantially contain particles of 0 μm or more, for the following reason. Average particle size is 8μm
If it is less than 10 μm, the fluidity will be extremely reduced and the toner will easily scatter, and if it exceeds 10 μm, the toner adhering to the literature area will be noticeable on the printed image, the resolution will decrease, and particles with a particle size of 20 μm or more will This is because if a large amount of .
本発明を以下の実施例により具体的に説明する。 The present invention will be specifically explained with reference to the following examples.
スチレン・アクリル系共重合体(三洋化成製ハイマーS
BM600)77重量部、カーボンブラック(三菱化成
製#50)10重置部、低分子量ポリプロピレン(三洋
化成製ビスコール550 P)3重量部、帯電制御剤(
オリエント化学製ボントロン554)2重量部、炭化ケ
イ素微粉末(昭和電工製DU−AI、平均粒径0.45
.um)1重量部、CaC03(日東粉化工業製NS#
2500、平均粒径0.89μm)7重量部をボールミ
ルで乾式混合し、ニーダにより加熱混練し、冷却値化後
ジェットミルで粉砕し、分級して5トナ一粒子を作成し
た。Styrene/acrylic copolymer (Himer S manufactured by Sanyo Chemical Co., Ltd.
BM600) 77 parts by weight, carbon black (Mitsubishi Kasei #50) 10 parts by weight, low molecular weight polypropylene (Sanyo Kasei Viscole 550 P) 3 parts by weight, charge control agent (
Orient Chemical Bontron 554) 2 parts by weight, silicon carbide fine powder (Showa Denko DU-AI, average particle size 0.45)
.. um) 1 part by weight, CaC03 (Nitto Funka Kogyo NS#
2500, average particle size 0.89 μm) were dry mixed in a ball mill, heated and kneaded in a kneader, cooled and crushed in a jet mill, and classified to produce one particle of 5 toner.
次に上記トナー粒子に疎水性コロイダルシリカ(疎水性
指数60、平均粒径16nm)とポリメチルメタクリレ
ート(以下PMMAという、平均粒径0.4μm、ガラ
ス転移温度53℃)の微粉末とを添加し、ヘンシェルミ
キサーで混合してトナーを製造した。ここでシリカとP
MMAの微粒子の添加量を変化させて表1に示す7種類
のトナーを製造した。各トナーの平均粒径は9μmで、
又各トナーとも20μm以上の粒子の含有量は2重量%
であった。Next, fine powder of hydrophobic colloidal silica (hydrophobicity index 60, average particle size 16 nm) and polymethyl methacrylate (hereinafter referred to as PMMA, average particle size 0.4 μm, glass transition temperature 53° C.) was added to the above toner particles. , and mixed in a Henschel mixer to produce a toner. Here silica and P
Seven types of toners shown in Table 1 were manufactured by varying the amount of MMA fine particles added. The average particle size of each toner is 9 μm,
In addition, the content of particles of 20 μm or more in each toner is 2% by weight.
Met.
なお上記のコロイダルシリカは次の手順により作成した
。まず市販のコロイダルシリカ(日本アエロジル製アエ
ロジル#130)10重置部を高速回転ミキサーに投入
し、8000r、p、m、で回転させながら、ヘキサメ
チルジシラザン1重量部をヘキサン8重量部で希釈した
溶液を滴下し分散させた。Note that the above colloidal silica was created by the following procedure. First, 10 parts of commercially available colloidal silica (Aerosil #130 manufactured by Nippon Aerosil) were placed in a high-speed rotating mixer, and while rotating at 8000 r, p, m, 1 part by weight of hexamethyldisilazane was diluted with 8 parts by weight of hexane. The solution was added dropwise and dispersed.
次いで得られたパウダーリキッドを150℃で4時間加
熱攪拌することにより疎水化されたコロイダルシリカと
した。Next, the obtained powder liquid was heated and stirred at 150° C. for 4 hours to obtain hydrophobized colloidal silica.
またPMMAの微粒子は以下の手順で作成した。Further, PMMA fine particles were created according to the following procedure.
攪拌機、温度計、窒素導入管、還流冷却器を装着したI
Eの四つロフラスコに、メチルヌククリレート100重
量部、蒸留水300重量部を入れ、開始剤として過硫酸
カリウムとチオ硫酸ナトリウムとからなるレドックス触
媒を5 X 10−’won!e/lとなるように添加
し、窒素気流中60℃で2゜時間反応を行なった。その
後液温が20℃になる−で冷却し、ろ過装置および熱風
乾燥器を使用してPMMAの微粒子を得た。I equipped with a stirrer, thermometer, nitrogen inlet tube, and reflux condenser
100 parts by weight of methyl nucleate and 300 parts by weight of distilled water were placed in a four-bottle flask (E), and a redox catalyst consisting of potassium persulfate and sodium thiosulfate was added as an initiator at 5 x 10-'won! The mixture was added at a ratio of e/l, and the reaction was carried out at 60° C. for 2 hours in a nitrogen stream. Thereafter, the solution was cooled to a temperature of 20° C., and PMMA fine particles were obtained using a filtration device and a hot air dryer.
上記の各トナーを用いてOPC感光体上の静電荷像を現
像し、得られたトナー像を普通紙に転写し、次いでヒー
トロール定着(定着温度165℃、定着圧力1kg/a
m)を行なった。現像は、第1図において、スリーブ1
を65 tm/secの速度で回転させ、ドクターギャ
ップを0.05mmに設定し、感光体10とスリーブl
とを略コンタクトの状態に設置し、スリーブ1とドクタ
一部材6との間に一80vの直流バイアス電圧を印加し
て行なった。The electrostatic charge image on the OPC photoreceptor is developed using each of the above toners, the resulting toner image is transferred to plain paper, and then heat roll fixing (fixing temperature 165°C, fixing pressure 1 kg/a
m) was carried out. The development is performed using sleeve 1 in FIG.
was rotated at a speed of 65 tm/sec, the doctor gap was set to 0.05 mm, and the photoreceptor 10 and sleeve l were
The test was carried out by placing the sleeve 1 and the doctor member 6 in a substantially contact state, and applying a DC bias voltage of -80 V between the sleeve 1 and the doctor member 6.
得られた画像の評価結果も同じく表1に示す。The evaluation results of the obtained images are also shown in Table 1.
上表の結果から、シリカとPMMAを共に添加しないト
ナー(磁1)を用いた場合は、定着性は良いが、スリー
ブ表面にトナーの付着を生ずることがわかる。またシリ
カのみを添加したトナー(磁2〜4)を用いた場合は、
スリーブ表面へのトナーの付着は防止できるが定着性が
低下してしまうことがわかる。From the results in the table above, it can be seen that when a toner (Magnetic 1) to which neither silica nor PMMA is added is used, the fixing performance is good, but the toner adheres to the sleeve surface. In addition, when using toner containing only silica (Magnetic 2 to 4),
It can be seen that although toner adhesion to the sleeve surface can be prevented, the fixing performance is reduced.
これに対して本発明のトナー(!lh5〜7)を用いた
場合は、スリーブ表面へのトナーの付着は無くなり、又
定着性も良いことがわかる。ただしPMMAの添加量が
多すぎると(m8)、地力ブリが生じ、又シリカの添加
量が多すぎると(隘9)定着性が低下する。On the other hand, when the toners of the present invention (!lh5-7) were used, it was found that the toner did not adhere to the sleeve surface and had good fixing properties. However, if the amount of PMMA added is too large (m8), burr will occur, and if the amount of silica added is too large (9), the fixing performance will be reduced.
本発明は、トナー搬送体上へのトナー付着防止を主目的
とするものであるからして、本発明のトナーは第1図お
よび第2図の装置以外に適用した場合でも上記と同様の
効果が得られることはもちろんである。Since the main purpose of the present invention is to prevent toner from adhering to the toner conveying body, the toner of the present invention can provide the same effects as described above even when applied to devices other than those shown in FIGS. 1 and 2. Of course, it is possible to obtain
以上の通り、本発明のトナーは、研摩剤微粒子を含むト
ナー粒子の表面に疎水性シリカと樹脂微粒子が添加され
ているので、例えば電極付誘電性スリーブを用いた非磁
性1成分方式に適用することにより、多数枚の複写を行
なってもスリーブ表面へのトナーの付着が有効に防止さ
れ、かつ、良好な定着性も有する高品質の画像を得るこ
とができる。As described above, the toner of the present invention has hydrophobic silica and resin particles added to the surface of the toner particles including abrasive particles, so it can be applied to, for example, a non-magnetic one-component system using a dielectric sleeve with an electrode. This effectively prevents toner from adhering to the sleeve surface even when a large number of copies are made, and it is possible to obtain high-quality images with good fixing properties.
第1図は本発明のトナーを用いる現像装置の一例を示す
概略断面図、第2図は第1図におけるスリーブを模式的
に示した図である。
1ニスリーブ、2:基体、3:誘電体層、4:微小電極FIG. 1 is a schematic sectional view showing an example of a developing device using the toner of the present invention, and FIG. 2 is a diagram schematically showing the sleeve in FIG. 1. 1 sleeve, 2: substrate, 3: dielectric layer, 4: microelectrode
Claims (1)
磁性粒子の表面に疎水性シリカと平均粒径1μm以下の
樹脂微粒子とを添加したトナー粒子からなり、前記トナ
ー粒子は平均粒径が8〜10μmの範囲にあり、かつ、
粒径20μm以上の粒子を実質的に含まないような粒度
分布を有することを特徴とする静電荷像現像用トナー。(1) Toner particles are made of non-magnetic particles containing a binder resin, a colorant, and abrasive particles, and hydrophobic silica and resin particles with an average particle size of 1 μm or less are added to the surface of the toner particles, and the toner particles are average particles. The diameter is in the range of 8 to 10 μm, and
A toner for developing an electrostatic image, characterized by having a particle size distribution that substantially does not contain particles with a particle size of 20 μm or more.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62258716A JPH01101557A (en) | 1987-10-14 | 1987-10-14 | Toner for developing electrostatic charge image |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62258716A JPH01101557A (en) | 1987-10-14 | 1987-10-14 | Toner for developing electrostatic charge image |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH01101557A true JPH01101557A (en) | 1989-04-19 |
Family
ID=17324101
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP62258716A Pending JPH01101557A (en) | 1987-10-14 | 1987-10-14 | Toner for developing electrostatic charge image |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH01101557A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01126665A (en) * | 1987-11-12 | 1989-05-18 | Konica Corp | Image forming method |
| JPH01234859A (en) * | 1988-03-16 | 1989-09-20 | Konica Corp | Image forming method |
| JPH0364764A (en) * | 1989-08-03 | 1991-03-20 | Canon Inc | color toner |
| WO1992018909A1 (en) * | 1991-04-19 | 1992-10-29 | Fujitsu Limited | Non-magnetic component developing method |
-
1987
- 1987-10-14 JP JP62258716A patent/JPH01101557A/en active Pending
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01126665A (en) * | 1987-11-12 | 1989-05-18 | Konica Corp | Image forming method |
| JPH01234859A (en) * | 1988-03-16 | 1989-09-20 | Konica Corp | Image forming method |
| JPH0364764A (en) * | 1989-08-03 | 1991-03-20 | Canon Inc | color toner |
| WO1992018909A1 (en) * | 1991-04-19 | 1992-10-29 | Fujitsu Limited | Non-magnetic component developing method |
| US5589313A (en) * | 1991-04-19 | 1996-12-31 | Fujitsu, Ltd. | Method for nonmagnetic monocomponent development |
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