JPH04260061A - Method for recording image - Google Patents
Method for recording imageInfo
- Publication number
- JPH04260061A JPH04260061A JP3042788A JP4278891A JPH04260061A JP H04260061 A JPH04260061 A JP H04260061A JP 3042788 A JP3042788 A JP 3042788A JP 4278891 A JP4278891 A JP 4278891A JP H04260061 A JPH04260061 A JP H04260061A
- Authority
- JP
- Japan
- Prior art keywords
- image
- toner
- magnetic
- carrier
- weight
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000000034 method Methods 0.000 title claims abstract description 22
- 239000000463 material Substances 0.000 claims abstract description 5
- 239000004020 conductor Substances 0.000 claims abstract description 3
- 238000005243 fluidization Methods 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 description 16
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 13
- 239000011347 resin Substances 0.000 description 8
- 229920005989 resin Polymers 0.000 description 8
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- 239000000377 silicon dioxide Substances 0.000 description 6
- 239000000975 dye Substances 0.000 description 5
- 108091008695 photoreceptors Proteins 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 239000003086 colorant Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 230000002209 hydrophobic effect Effects 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- -1 polypropylene Polymers 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 229910018404 Al2 O3 Inorganic materials 0.000 description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000010298 pulverizing process Methods 0.000 description 3
- 229910000859 α-Fe Inorganic materials 0.000 description 3
- 229910002012 Aerosil® Inorganic materials 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 235000010216 calcium carbonate Nutrition 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 229910052681 coesite Inorganic materials 0.000 description 2
- 229910052593 corundum Inorganic materials 0.000 description 2
- 229910052906 cristobalite Inorganic materials 0.000 description 2
- 239000006247 magnetic powder Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 229910052682 stishovite Inorganic materials 0.000 description 2
- 229910052905 tridymite Inorganic materials 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- 229910001845 yogo sapphire Inorganic materials 0.000 description 2
- OSNILPMOSNGHLC-UHFFFAOYSA-N 1-[4-methoxy-3-(piperidin-1-ylmethyl)phenyl]ethanone Chemical compound COC1=CC=C(C(C)=O)C=C1CN1CCCCC1 OSNILPMOSNGHLC-UHFFFAOYSA-N 0.000 description 1
- 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
- MFYSUUPKMDJYPF-UHFFFAOYSA-N 2-[(4-methyl-2-nitrophenyl)diazenyl]-3-oxo-n-phenylbutanamide Chemical compound C=1C=CC=CC=1NC(=O)C(C(=O)C)N=NC1=CC=C(C)C=C1[N+]([O-])=O MFYSUUPKMDJYPF-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
- 235000010919 Copernicia prunifera Nutrition 0.000 description 1
- 244000180278 Copernicia prunifera Species 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
- 241000220317 Rosa Species 0.000 description 1
- 230000000996 additive effect 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
- 239000011230 binding agent Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000000969 carrier 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
- 238000001816 cooling Methods 0.000 description 1
- 229920001577 copolymer Polymers 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
- 238000000151 deposition Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000007429 general method Methods 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
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 1
- 238000004898 kneading Methods 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
- 230000007774 longterm Effects 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229920003146 methacrylic ester copolymer Polymers 0.000 description 1
- YLGXILFCIXHCMC-JHGZEJCSSA-N methyl cellulose Chemical compound COC1C(OC)C(OC)C(COC)O[C@H]1O[C@H]1C(OC)C(OC)C(OC)OC1COC YLGXILFCIXHCMC-JHGZEJCSSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 239000006082 mold release agent Substances 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
- 239000002994 raw material Substances 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
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 1
- 239000008030 superplasticizer Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 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
- 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
Landscapes
- Dry Development In Electrophotography (AREA)
- Developing Agents For Electrophotography (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は、電子写真、静電印刷等
の手段において、担持体上に静電荷像を形成し、この担
持体の非画像部(露光部)に非磁性一成分系のトナーを
付着させて画像を形成する所謂反転現像による画像記録
方法に関するものである。[Industrial Application Field] The present invention is directed to forming an electrostatic charge image on a carrier by means of electrophotography, electrostatic printing, etc. The present invention relates to an image recording method using so-called reversal development in which an image is formed by depositing toner.
【0002】0002
【従来の技術】従来、電子写真法、静電印刷法等におい
ては、種々の手段によって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って現像して可視的な
トナー像とし、この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通常である。[Prior Art] Conventionally, in electrophotography, electrostatic printing, etc., an electrostatic charge image is formed on the surface of a photoreceptor by various means, and this electrostatic charge image is developed with toner to produce a visible toner image. Usually, this toner image is transferred to plain paper or the like and then fixed to obtain a final image.
【0003】次に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おいて
は、鉄粉若しくはフェライト粉末等のキャリアと、樹脂
および着色剤を主体とするトナーとの混合粉体である二
成分系現像剤を使用する方式が従来から多用されている
。しかしながら上記二成分系の現像剤を使用する場合に
おいては、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であると共に、長時間の使用におい
てキャリアの表面がトナーによって汚染され、キャリア
の摩擦帯電能力が低下する等の欠点がある。[0003] Next, a general method for developing an electrostatic image is a magnetic brush method. In this magnetic brush method, a carrier such as iron powder or ferrite powder and a toner mainly composed of a resin and a colorant are used. Conventionally, a method using a two-component developer which is a powder mixture of However, when using the above two-component developer, the mixing ratio of toner and carrier (toner concentration)
Since the image quality will not be stable unless strictly controlled, a means of controlling the toner concentration is required, and there are also drawbacks such as the surface of the carrier becoming contaminated with toner during long-term use and the triboelectric charging ability of the carrier being reduced. .
【0004】これらの欠点を解消するために、樹脂と磁
性粉とを主体とする磁性トナーを使用する一成分系現像
法が開発され、実用化されている。なおこの一成分系現
像法においては、良好な転写性を得るために絶縁性の磁
性トナーを使用することが多い(例えば特開昭53−3
1136号公報参照)。また現像方法についても種々の
方法が提案されているが、トナー相互の摩擦若しくはト
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。[0004] In order to eliminate 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 this one-component development method, insulating magnetic toner is often used to obtain good transferability (for example, as disclosed in Japanese Patent Laid-Open No. 53-3
(See Publication No. 1136). Also, various methods have been proposed for developing methods, but a method in which toner is triboelectrically charged by friction between toners or friction between toner and a sleeve or the like is often used.
【0005】しかしながらトナーの摩擦帯電を利用する
現像法においては、トナーが凝集し易く、また環境条件
によって画質が変化し易いという欠点がある。更に磁性
トナーは例えばマグネタイト等の磁性粉を20〜70重
量%程度含有するため、前記二成分系現像剤より定着性
が劣るという欠点がある。However, the developing method that utilizes toner triboelectric charging has the drawback that the toner tends to aggregate and the image quality tends to change depending on environmental conditions. Furthermore, since the magnetic toner contains about 20 to 70% by weight of magnetic powder such as magnetite, it has a drawback that its fixing properties are inferior to those of the two-component developer.
【0006】上記のような欠点を解消するものとして、
非磁性一成分系のトナーのみを使用する画像記録方法も
出現している。[0006] As a solution to the above-mentioned drawbacks,
Image recording methods using only non-magnetic one-component toner have also appeared.
【0007】図1は非磁性一成分系のトナーを使用する
現像装置の例を示す要部説明図である。図1において、
1は現像ロールであり、アルミニウム若しくはステンレ
ス鋼のような非磁性金属材料等により円筒状に形成し、
トナー2を収容するトナー槽3の下部に回転自在に設け
られている。4は可撓性材料からなるブレードであり、
トナー槽3に固着されると共に、その自由端が現像ロー
ル1の表面と面接触し、かつ摺動係合するように配設さ
れている。なお現像ロール1にはバイアス電圧源5を接
続すると共に、負の帯電極性を有する有機光導電材料か
らなり、静電荷像を担持する感光体6と若干の間隔を介
して対向配設する。矢印は現像ロール1および感光体6
の回転方向を示している。FIG. 1 is an explanatory diagram of the main parts of an example of a developing device using non-magnetic one-component toner. In Figure 1,
1 is a developing roll, which is formed into a cylindrical shape from a non-magnetic metal material such as aluminum or stainless steel;
It is rotatably provided at the lower part of the toner tank 3 that accommodates the toner 2 . 4 is a blade made of flexible material;
It is fixed to the toner tank 3 and disposed such that its free end is in surface contact with the surface of the developing roll 1 and slidably engaged therewith. A bias voltage source 5 is connected to the developing roll 1, and the developing roll 1 is disposed facing a photoreceptor 6, which is made of an organic photoconductive material having a negative charge polarity and carries an electrostatic image, with a slight distance therebetween. Arrows indicate developing roll 1 and photoreceptor 6
indicates the direction of rotation.
【0008】上記の構成により、現像ロール1を矢印方
向に回転させると、トナー槽3内のトナー2はブレード
4によって負の極性に帯電され、現像ロール1の表面に
静電力によって薄層を形成して付着し、感光体6に搬送
され、そして現像ロール1には静電荷像の電位より低い
電位のバイアス電圧が印加されるから、感光体6の表面
に形成された静電荷像(図示せず)の非画像部に付着し
、所謂反転現像を行うことができるのである。With the above configuration, when the developing roll 1 is rotated in the direction of the arrow, the toner 2 in the toner tank 3 is charged to a negative polarity by the blade 4, and a thin layer is formed on the surface of the developing roll 1 by electrostatic force. The electrostatic charge image (not shown) formed on the surface of the photoreceptor 6 is transferred to the photoconductor 6, and a bias voltage lower than the potential of the electrostatic charge image is applied to the developing roll 1. It adheres to the non-image areas of (1) and can perform so-called reversal development.
【0009】[0009]
【発明が解決しようとする課題】上記従来の非磁性一成
分系現像装置においては、現像用のトナーとしては、結
着用樹脂と着色剤を主体とするトナー粒子の表面に、疎
水性シリカを若干量添加してなる負の帯電極性を有する
トナーを使用するのが一般である。この場合において疎
水性シリカはトナー粒子の流動性改質剤若しくは流動化
剤として添加されるものである。[Problems to be Solved by the Invention] In the conventional non-magnetic one-component developing device described above, the developing toner is made by adding a small amount of hydrophobic silica to the surface of toner particles mainly consisting of a binding resin and a colorant. Generally, a toner having a negative charge polarity is used. In this case, hydrophobic silica is added as a fluidity modifier or fluidizing agent for toner particles.
【0010】しかしながら、上記流動化剤として使用さ
れる疎水性シリカは、摩擦帯電量が本来的に大であるた
め(−300〜−1000μc/g)、疎水性シリカを
流動化剤として添加したトナーを使用すると、静電荷像
の未露光部に、強く負に帯電したトナー若しくは正に帯
電したトナーが付着し、地カブリが発生し易く、画質を
低下させるという問題点がある。However, since the hydrophobic silica used as the fluidizing agent has a inherently large amount of triboelectric charge (-300 to -1000 μc/g), toners containing hydrophobic silica as a fluidizing agent When used, there is a problem that strongly negatively charged toner or positively charged toner adheres to the unexposed portions of the electrostatic image, which tends to cause background fog and deteriorate image quality.
【0011】本発明は上記従来技術に存在する問題点を
解決し、地カブリの発生を防止し、かつ画像濃度および
解像度が優れた高品質の画像を得ることができる画像記
録方法を提供することを目的とする。[0011] The present invention solves the problems existing in the above-mentioned prior art, and provides an image recording method that can prevent the occurrence of background fog and obtain high-quality images with excellent image density and resolution. With the goal.
【0012】0012
【課題を解決するための手段】上記目的を達成するため
に、本発明においては、負の帯電特性を有する有機光導
電材料からなる担持体上に静電荷像を形成し、この担持
体の非画像部に、導電材料により円筒状に形成してなる
現像ロールを介して搬送した非磁性一成分系のトナーを
付着させて画像を形成する画像記録方法において、摩擦
帯電量が−10〜−100μc/gの流動化剤を0.0
1〜1.5重量部添加してなる非磁性一成分系のトナー
を使用する、という技術的手段を採用した。このような
流動化剤としては、例えばAl2 O3 (アルミナ)
、TiO2 (酸化チタン)を使用することができる。[Means for Solving the Problems] In order to achieve the above object, in the present invention, an electrostatic charge image is formed on a carrier made of an organic photoconductive material having negative charging characteristics, and In an image recording method in which an image is formed by attaching non-magnetic one-component toner conveyed via a cylindrical developing roll made of a conductive material to an image area, the amount of triboelectric charge is -10 to -100 μc. /g of superplasticizer to 0.0
A technical measure was adopted in which a non-magnetic one-component toner containing 1 to 1.5 parts by weight was used. As such a fluidizing agent, for example, Al2 O3 (alumina)
, TiO2 (titanium oxide) can be used.
【0013】本発明において、流動化剤の摩擦帯電量が
−100μc/gを超えると地カブリを発生し、画質を
低下させるため不都合である。また上記摩擦帯電量が−
10μc/g未満になると、トナーと流動化剤とが分離
し、充分な流動化作用が得られなくなるため好ましくな
い。In the present invention, if the amount of triboelectric charge of the fluidizing agent exceeds -100 .mu.c/g, it is disadvantageous because background fog occurs and the image quality deteriorates. In addition, the amount of triboelectric charge mentioned above is −
If it is less than 10 μc/g, the toner and the fluidizing agent will separate and a sufficient fluidizing effect will not be obtained, which is not preferable.
【0014】次に流動化剤の添加量が0.01重量部未
満では、やはりトナーの流動性を改質する作用が不充分
であり、一方1.5重量部を超えるとトナーの摩擦帯電
量が大となって地カブリを発生するため好ましくない。Next, if the amount of the fluidizing agent added is less than 0.01 part by weight, the effect of modifying the fluidity of the toner is still insufficient, while if it exceeds 1.5 parts by weight, the amount of triboelectrification of the toner will decrease. This is undesirable because it becomes large and causes ground fog.
【0015】本発明において使用するトナー中に含有さ
せる結着用の樹脂としては、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
ステル共重合体、スチレン・メタクリル酸エステル共重
合体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若しくは混合して使
用することができる。[0015] Examples of the binding resin to be contained in the toner used in the present invention include polystyrene, styrene/butadiene copolymer, styrene/acrylic ester copolymer, styrene/methacrylic ester copolymer, and the like. Known toner resins such as styrene resins, epoxy resins, and polyester resins can be used alone or in combination.
【0016】また着色剤としては、カーボンブラック、
クロムイエロー、ハンザイエロー、ベンチジンイエロー
、ローズベンガラ、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若しくは染料を使用することができ
る。なお含有量は3〜10重量%が望ましい。[0016] As the coloring agent, carbon black,
Known pigments or dyes such as chrome yellow, Hansa yellow, benzidine yellow, rose red red, aniline red, phthalocyanine blue, aniline blue, nigrosine dye, and aniline black can be used. Note that the content is preferably 3 to 10% by weight.
【0017】本発明において使用するトナーは、上記結
着樹脂および着色剤と共に、帯電制御剤、離型剤、充填
剤等の他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)アゾ染料等、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、アミドワックス等、および充填剤としては
、炭酸カルシウム、タルク、クレイ等の無機微粉末が夫
々挙げられる。上記の添加物の含有量は、トナーに要求
される特性に応じて適宜選定されるが、一般に帯電制御
剤が1〜5重量%、離型剤が1〜5重量%および充填剤
が1〜10重量%であるのが通常である。[0017] The toner used in the present invention may contain other additives such as a charge control agent, a mold release agent, and a filler in addition to the above-mentioned binder resin and colorant. 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. Examples of the wax, amide wax, etc., and fillers include inorganic fine powders such as calcium carbonate, talc, and clay. The contents of the above additives are appropriately selected depending on the properties required of the toner, but generally the charge control agent is 1 to 5% by weight, the release agent is 1 to 5% by weight, and the filler is 1 to 5% by weight. It is usually 10% by weight.
【0018】本発明において使用するトナーは、粉砕法
、スプレードライ法等の公知の手段によって製造するこ
とができる。粉砕法による場合には、夫々の原料をボー
ルミル、乾式ミキサー等によって予備混合し、ニーダ、
ロール等により加熱混練し、冷却固化後ジェットミル等
で粉砕し、次いで分級することにより得られる。なおト
ナーの平均粒径は、画質の点から5〜20μmの範囲と
するのがよい。The toner used in the present invention can be manufactured by known means such as a pulverization method and a spray drying method. When using the pulverization method, the raw materials are premixed using a ball mill, dry mixer, etc., and then mixed with a kneader,
It is obtained by heating and kneading with a roll or the like, cooling and solidifying, pulverizing with a jet mill or the like, and then classifying. Note that the average particle diameter of the toner is preferably in the range of 5 to 20 μm from the viewpoint of image quality.
【0019】[0019]
【作用】 上記の構成により、流動化剤の所定の
作用を確保しつつトナーの摩擦帯電量を適正に設定する
ことができ、地カブリのない高品質の画像を形成するこ
とができる。[Function] With the above configuration, it is possible to appropriately set the amount of triboelectric charge of the toner while ensuring the predetermined action of the fluidizing agent, and it is possible to form a high-quality image without background fog.
【0020】[0020]
【実施例】まずスチレン−アクリル系共重合体(三洋化
成製 ハイマーSBM600)77重量部、カーボン
ブラック(三菱化成製 #50)10重量部、低分子
量ポリプロピレン(三洋化成製 ビスコール550P
)3重量部、荷電制御剤(オリエント化学製 ボント
ロンE81)2重量部およびCaCO3 (日東粉化工
業製NS#2500)8重量部を乾式混合し、ニーダに
より加熱混合し、冷却固化後ジェットミルで粉砕し、分
級を行って5〜25μmの粒度を有するトナーを作製し
た。このトナーにAl2 O3 ,TiO2 およびS
iO2 (日本アエロジル社製アエロジルR972)を
夫々表1に示す量を外添して非磁性一成分系現像剤とし
た。[Example] First, 77 parts by weight of styrene-acrylic copolymer (Himer SBM600 manufactured by Sanyo Chemical), 10 parts by weight of carbon black (#50 manufactured by Mitsubishi Chemical), and low molecular weight polypropylene (Viscol 550P manufactured by Sanyo Chemical)
), 2 parts by weight of a charge control agent (Bontron E81 manufactured by Orient Chemical Co., Ltd.), and 8 parts by weight of CaCO3 (NS#2500 manufactured by Nitto Funka Kogyo Co., Ltd.) were dry mixed, heated and mixed in a kneader, cooled and solidified, and then mixed in a jet mill. It was crushed and classified to produce a toner having a particle size of 5 to 25 μm. This toner contains Al2 O3, TiO2 and S.
iO2 (Aerosil R972 manufactured by Nippon Aerosil Co., Ltd.) was externally added in the amounts shown in Table 1 to prepare a non-magnetic one-component developer.
【0021】これらの外添剤のキャリア(日立金属製
KBN100フェライトキャリア、74〜149μm
)に対するブローオフ法(東芝ケミカル社製 TB−
200型使用)による摩擦帯電量は、外添剤濃度を2.
0重量%としたとき、Al2 O3 が−50μc/g
、TiO2 が−80μc/g、SiO2 が−400
μc/gであった。また表1中の摩擦帯電量は、同一フ
ェライトキャリアを使用し、トナー濃度を5.0重量%
としたときの値を示す。[0021] Carriers for these external additives (manufactured by Hitachi Metals)
KBN100 ferrite carrier, 74-149μm
) against the blow-off method (Toshiba Chemical TB-
200 model)), the amount of triboelectrification is determined by adjusting the external additive concentration to 2.
When set to 0% by weight, Al2O3 is -50μc/g
, TiO2 -80μc/g, SiO2 -400
It was μc/g. In addition, the amount of triboelectric charge in Table 1 is calculated using the same ferrite carrier and a toner concentration of 5.0% by weight.
Shows the value when .
【0022】[0022]
【表1】[Table 1]
【0023】上記非磁性一成分系現像剤を使用し、前記
図1に示す現像装置により、負帯電特性を有するOPC
からなる感光体6上に形成された静電荷像(表面電位−
550V、残留電位−80V)を反転現像し、得られた
可視像を普通紙上に転写した後、ヒートロール定着(定
着温度165℃、定着圧力1kg/cm2 )を行って
得た画像を評価した結果を表1に併記する。Using the non-magnetic one-component developer described above and using the developing device shown in FIG.
Electrostatic charge image (surface potential -
550 V, residual potential -80 V), and the resulting visible image was transferred onto plain paper, followed by heat roll fixing (fixing temperature 165°C, fixing pressure 1 kg/cm2), and the resulting image was evaluated. The results are also listed in Table 1.
【0024】なお上記現像に際しては、図1に示す感光
体6を周速50mm/秒で回転させ、現像ロール1を周
速125mm/秒で回転させ、現像ロール1の表面の現
像剤の薄層の厚さを0.1mmとし、コンタクト現像と
した。また現像ロール1には直流−450Vのバイアス
電圧を印加した。In the above development, the photoreceptor 6 shown in FIG. 1 is rotated at a circumferential speed of 50 mm/sec, and the developing roll 1 is rotated at a circumferential speed of 125 mm/sec. The thickness of the film was set to 0.1 mm, and contact development was performed. Further, a bias voltage of -450 V DC was applied to the developing roll 1.
【0025】表1から明らかなように、まずNo.3に
おいては、摩擦帯電量が大きすぎるため、カブリの発生
が認められる。これは前述のようにSiO2 の固有の
摩擦帯電量が大であることに起因する。これに対してN
o.1およびNo.2においては、カブリのない高品質
の画像が得られている。As is clear from Table 1, first, No. In No. 3, the amount of triboelectric charge was too large, so fogging was observed. This is due to the fact that SiO2 has a large inherent triboelectric charge as described above. On the other hand, N
o. 1 and no. In No. 2, a high-quality image without fogging was obtained.
【0026】次に流動化剤の添加量による影響について
記述する。まずAl2 O3 無添加のNo.4におい
ては、流動性が悪く、現像ロール1上の搬送性が低下し
、現像ムラが発生した。また画像濃度も1.20に留ま
り、実用上問題のあるレベルに低下した。一方Al2
O3 を2.0重量%添加したNo.11においては、
地カブリが発生すると共に、過剰のAl2 O3 が現
像ロール1から飛散し、現像装置内部を汚染する現象が
認められた。これに対してNo.4〜No.10におい
ては、カブリもなく良好な画像が得られた。Next, the influence of the amount of fluidizing agent added will be described. First, No. 1 with no Al2 O3 added. In No. 4, the fluidity was poor, the transportability on the developing roll 1 was reduced, and uneven development occurred. Further, the image density remained at 1.20, which was a level that was problematic for practical use. On the other hand, Al2
No. 2 with 2.0% by weight of O3 added. In 11,
A phenomenon was observed in which background fog occurred and excessive Al2O3 was scattered from the developing roll 1, contaminating the inside of the developing device. On the other hand, No. 4~No. In No. 10, a good image was obtained without fogging.
【0027】[0027]
【発明の効果】本発明は以上記述のような構成および作
用であるから、流動化剤の所定の作用を確保しつつ、カ
ブリの発生を防止し、画像濃度および解像度が優れた高
品質の画像を得ることができるという効果がある。[Effects of the Invention] Since the present invention has the structure and operation as described above, it is possible to prevent the occurrence of fog while ensuring the predetermined action of the fluidizing agent, and to produce high-quality images with excellent image density and resolution. It has the effect of being able to obtain
【図1】非磁性一成分系のトナーを使用する現像装置の
例を示す要部説明図である。FIG. 1 is an explanatory view of the main parts of an example of a developing device that uses non-magnetic one-component toner.
1 現像ロール 2 トナー 1 Developing roll 2 Toner
Claims (1)
からなる担持体上に静電荷像を形成し、この担持体の非
画像部に、導電材料により円筒状に形成してなる現像ロ
ールを介して搬送した非磁性一成分系のトナーを付着さ
せて画像を形成する画像記録方法において、摩擦帯電量
が−10〜−100μc/gの流動化剤を0.01〜1
.5重量部添加してなる非磁性一成分系のトナーを使用
することを特徴とする画像記録方法。1. An electrostatic charge image is formed on a carrier made of an organic photoconductive material having negative charging characteristics, and a developing roll formed in a cylindrical shape made of a conductive material is placed in a non-image area of the carrier. In an image recording method in which an image is formed by adhering non-magnetic one-component toner conveyed through
.. An image recording method characterized by using a non-magnetic one-component toner containing 5 parts by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3042788A JP2870556B2 (en) | 1991-02-15 | 1991-02-15 | Image recording method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3042788A JP2870556B2 (en) | 1991-02-15 | 1991-02-15 | Image recording method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04260061A true JPH04260061A (en) | 1992-09-16 |
JP2870556B2 JP2870556B2 (en) | 1999-03-17 |
Family
ID=12645709
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3042788A Expired - Fee Related JP2870556B2 (en) | 1991-02-15 | 1991-02-15 | Image recording method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2870556B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006243057A (en) * | 2005-02-28 | 2006-09-14 | Kyocera Mita Corp | Developing device |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62200364A (en) * | 1986-02-27 | 1987-09-04 | Konishiroku Photo Ind Co Ltd | Development method for one-component developer |
JPS6477075A (en) * | 1987-06-15 | 1989-03-23 | Fuji Xerox Co Ltd | Device and method for development |
-
1991
- 1991-02-15 JP JP3042788A patent/JP2870556B2/en not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62200364A (en) * | 1986-02-27 | 1987-09-04 | Konishiroku Photo Ind Co Ltd | Development method for one-component developer |
JPS6477075A (en) * | 1987-06-15 | 1989-03-23 | Fuji Xerox Co Ltd | Device and method for development |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006243057A (en) * | 2005-02-28 | 2006-09-14 | Kyocera Mita Corp | Developing device |
JP4744164B2 (en) * | 2005-02-28 | 2011-08-10 | 京セラミタ株式会社 | Development device |
Also Published As
Publication number | Publication date |
---|---|
JP2870556B2 (en) | 1999-03-17 |
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