JPS63139366A - Production of developer for electrophotography - Google Patents
Production of developer for electrophotographyInfo
- Publication number
- JPS63139366A JPS63139366A JP61148090A JP14809086A JPS63139366A JP S63139366 A JPS63139366 A JP S63139366A JP 61148090 A JP61148090 A JP 61148090A JP 14809086 A JP14809086 A JP 14809086A JP S63139366 A JPS63139366 A JP S63139366A
- Authority
- JP
- Japan
- Prior art keywords
- developer
- silicic acid
- powder
- toner
- styrene
- 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
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 239000000843 powder Substances 0.000 claims abstract description 42
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 claims abstract description 31
- 235000012239 silicon dioxide Nutrition 0.000 claims abstract description 31
- 238000000034 method Methods 0.000 claims description 28
- 229920001577 copolymer Polymers 0.000 abstract description 23
- 239000002245 particle Substances 0.000 abstract description 15
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 abstract description 4
- 239000000203 mixture Substances 0.000 abstract description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 24
- 230000005291 magnetic effect Effects 0.000 description 16
- 108091008695 photoreceptors Proteins 0.000 description 15
- 239000000377 silicon dioxide Substances 0.000 description 11
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 8
- 239000004115 Sodium Silicate Substances 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical group [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 5
- 229910052911 sodium silicate Inorganic materials 0.000 description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000006247 magnetic powder Substances 0.000 description 4
- -1 polyP-chlorostyrene Polymers 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- 230000006378 damage Effects 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- 238000009825 accumulation Methods 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 239000011521 glass Substances 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
- 239000012188 paraffin wax Substances 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 238000010298 pulverizing process Methods 0.000 description 2
- 150000004760 silicates Chemical class 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- 229910000859 α-Fe Inorganic materials 0.000 description 2
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- FEIQOMCWGDNMHM-UHFFFAOYSA-N 5-phenylpenta-2,4-dienoic acid Chemical compound OC(=O)C=CC=CC1=CC=CC=C1 FEIQOMCWGDNMHM-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical class N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 239000013032 Hydrocarbon resin Substances 0.000 description 1
- BGPVFRJUHWVFKM-UHFFFAOYSA-N N1=C2C=CC=CC2=[N+]([O-])C1(CC1)CCC21N=C1C=CC=CC1=[N+]2[O-] Chemical compound N1=C2C=CC=CC2=[N+]([O-])C1(CC1)CCC21N=C1C=CC=CC1=[N+]2[O-] BGPVFRJUHWVFKM-UHFFFAOYSA-N 0.000 description 1
- 239000002033 PVDF binder Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004111 Potassium silicate Substances 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229920007962 Styrene Methyl Methacrylate Polymers 0.000 description 1
- 239000004110 Zinc silicate Substances 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 229910052915 alkaline earth metal silicate Inorganic materials 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229910001566 austenite Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000006258 conductive agent Substances 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- ZOIVSVWBENBHNT-UHFFFAOYSA-N dizinc;silicate Chemical compound [Zn+2].[Zn+2].[O-][Si]([O-])([O-])[O-] ZOIVSVWBENBHNT-UHFFFAOYSA-N 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000005294 ferromagnetic effect Effects 0.000 description 1
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 1
- 229920006270 hydrocarbon resin Polymers 0.000 description 1
- UCNNJGDEJXIUCC-UHFFFAOYSA-L hydroxy(oxo)iron;iron Chemical compound [Fe].O[Fe]=O.O[Fe]=O UCNNJGDEJXIUCC-UHFFFAOYSA-L 0.000 description 1
- 239000003456 ion exchange resin Substances 0.000 description 1
- 229920003303 ion-exchange polymer Polymers 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- 239000006249 magnetic particle Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- ADFPJHOAARPYLP-UHFFFAOYSA-N methyl 2-methylprop-2-enoate;styrene Chemical compound COC(=O)C(C)=C.C=CC1=CC=CC=C1 ADFPJHOAARPYLP-UHFFFAOYSA-N 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001490 poly(butyl methacrylate) polymer Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002102 polyvinyl toluene Polymers 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- NNHHDJVEYQHLHG-UHFFFAOYSA-N potassium silicate Chemical compound [K+].[K+].[O-][Si]([O-])=O NNHHDJVEYQHLHG-UHFFFAOYSA-N 0.000 description 1
- 229910052913 potassium silicate Inorganic materials 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- SCUZVMOVTVSBLE-UHFFFAOYSA-N prop-2-enenitrile;styrene Chemical compound C=CC#N.C=CC1=CC=CC=C1 SCUZVMOVTVSBLE-UHFFFAOYSA-N 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 235000019794 sodium silicate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 229920000638 styrene acrylonitrile Polymers 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 235000019352 zinc silicate Nutrition 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
- G03G9/087—Binders for toner particles
- G03G9/08702—Binders for toner particles comprising macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- G03G9/08726—Polymers of unsaturated acids or derivatives thereof
- G03G9/08728—Polymers of esters
-
- 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
- G03G9/09708—Inorganic compounds
- G03G9/09725—Silicon-oxides; Silicates
Landscapes
- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- General Physics & Mathematics (AREA)
- Inorganic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Spectroscopy & Molecular Physics (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、静電記録、静’i[印刷等におけ
る静荷電像を現像するための現像剤の製造方法に関する
。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a method for producing a developer for developing electrostatically charged images in electrophotography, electrostatic recording, static printing, etc.
[従来の技術]
従来、電子写真法としては米国特許第2.297゜89
1号明細書等、多数の方法が知られているが、一般には
光導電性物質を利用し1種々の手段により感光体上に電
気的潜像を形成し、次いで該潜像を現像粉(以下トナー
と称す)を用いて現像し、必要に応じて紙等の転写材に
トナー画像を転写した後、加熱、圧力あるいは溶剤蒸気
などにより定着し複写物を得るものである。またトナー
画像を転写する工程を有する場合には、通常感光体上の
残余のトナーを除去するための工程が設けられる。[Prior Art] Conventionally, as an electrophotographic method, U.S. Patent No. 2.297°89
Although a number of methods are known, such as in the specification of No. 1, in general, an electrical latent image is formed on a photoreceptor by various means using a photoconductive substance, and then the latent image is transferred to a developing powder ( After the toner image is transferred to a transfer material such as paper as necessary, it is fixed by heat, pressure, solvent vapor, etc. to obtain a copy. Further, when a step of transferring a toner image is included, a step for removing residual toner on the photoreceptor is usually provided.
電気的潜像をトナーを用いて可視化する方法は、例えば
米国特許第2.874.083号明細書に記載されてい
る磁気ブラシ法、同2,818,552号明細書に記載
されているカスケード現像法及び同2,221゜776
号明細書に記載されている粉末雲法、米国特許第3.9
09.258号明細書に記載されている導電性の磁性ト
ナーを用いる方法、特公昭41−9475号公報等に記
載されている種々の絶縁性の磁性トナーを用いる方法な
どが知られている。Examples of methods for visualizing electrical latent images using toner include the magnetic brush method described in U.S. Pat. No. 2,874,083, and the cascade method described in U.S. Pat. No. 2,818,552. Development method and 2,221°776
The powder cloud method described in US Pat. No. 3.9
A method using a conductive magnetic toner described in Japanese Patent Publication No. 09.258, a method using various insulating magnetic toners described in Japanese Patent Publication No. 41-9475, etc. are known.
これらの現像法に適用するトナーとしては、従来、天然
あるいは合成樹脂中に染料、顔料を分散させた微粉末が
使用されている。例えば、ポリスチレンなどの結着樹脂
中に着色剤を分散させたものを1〜30終層程度に微粉
砕した粒子がトナーとして用いられている。磁性トナー
としてはマグネタイトなどの磁性体粒子を含有せしめた
ものが用いられている。いわゆる二成分現像剤を用いる
方式の場合には、トナーは通常ガラスピーズ、鉄粉など
のキャリアー粒子と混合されて用いられる。As toners applied to these developing methods, fine powders in which dyes and pigments are dispersed in natural or synthetic resins have conventionally been used. For example, particles obtained by dispersing a colorant in a binder resin such as polystyrene and pulverizing the particles to about 1 to 30 layers are used as toner. As the magnetic toner, one containing magnetic particles such as magnetite is used. In the case of a system using a so-called two-component developer, the toner is usually mixed with carrier particles such as glass beads and iron powder.
従来トナーにコロイダルシリカと称されるケイ酸微粉末
を添加する例は公知であり、その添加によってトナーに
流動性を付与し、さらに、トナーの荷電性を均一にする
効果があることが認められる。しかしながら従来のケイ
酸微粉末を含有したトナーでは、コピーを続けるにつれ
て感光体上のケイ酸微粉末をクリーニングしきれず、し
だいに付着し、感光体上にフィルミングが発生する。そ
のためコントラストの低下、印字背景部のカブリが著し
くなる問題点があった。Examples of adding silicic acid fine powder called colloidal silica to conventional toners are well known, and it is recognized that the addition has the effect of imparting fluidity to toners and furthermore uniformizing the chargeability of the toners. . However, with conventional toner containing fine silicic acid powder, as copying continues, the fine silicic acid powder on the photoreceptor cannot be completely cleaned and gradually adheres to the photoreceptor, resulting in filming on the photoreceptor. As a result, there were problems in that the contrast deteriorated and the background portion of the print became significantly fogged.
本発明者らは、上述の問題点を解決するため検討した結
果、トナーが含有するケイ酸微粉末中、トナーに付着し
ていないケイ酸微粉末(以下′M離クシリカ称す)がフ
ィルミングを発生する原因であることをつきとめた。As a result of studies to solve the above-mentioned problems, the present inventors found that among the silicic acid fine powders contained in the toner, the silicic acid fine powders (hereinafter referred to as ``M-release silica'') that are not attached to the toner cause filming. It was determined that this was the cause.
すなわち、これについて説明すると、転写後の感光体ク
リーナーによりかき取られたトナー中のケイ酸含有量を
調べたところ、現像前のトナーのそれに比べて増加して
おり、さらにクリーナー中のトナーを電子顕微鏡で既察
するとケイ酸微粉末の凝集体と認めることのできた粒子
がトナー粒子に付着することなく存在するのが数多く認
められた。また感光体上のフィルミングの発生した箇所
を分析したところ、ケイ酸及び転写紙粉が主な成分であ
ることが判明した。In other words, to explain this, when we investigated the silicic acid content in the toner scraped off by the photoreceptor cleaner after transfer, we found that it had increased compared to that in the toner before development. When observed under a microscope, many particles that could be recognized as aggregates of fine silicic acid powder were observed to exist without adhering to the toner particles. Further, when the location on the photoreceptor where filming occurred was analyzed, it was found that silicic acid and transfer paper powder were the main components.
本発明者らは、この結果から、トナー中の遊離シリカを
除去することで上述の問題点を解決できることを見い出
した。Based on these results, the present inventors have found that the above-mentioned problems can be solved by removing free silica in the toner.
本発明を適用できる現像工程の例を説明する。An example of a developing process to which the present invention can be applied will be explained.
第1図に現像工程の一実施形態を断面図で示す。FIG. 1 shows a cross-sectional view of one embodiment of the developing process.
同図において静電像保持体1は矢印方向に動く。In the figure, the electrostatic image holder 1 moves in the direction of the arrow.
現像剤担体である非磁性円筒2は、現像部において静電
像保持体表面と同方向に進むように回転する。非磁性円
筒2の内部には、多極永久磁石3が回転しないように配
されている。現像剤容器4から送られる一成分系絶縁性
磁性現像剤6を非磁性円筒面上に塗布し、かつ円筒面と
トナー粒子との摩擦によって、トナー粒子に静電像電荷
と逆極性の荷電を与える。さらに鉄製のドクターブレー
ド5を円筒表面に近接して(間隔50μ11〜500u
+* )、多極永久磁石3の一つの磁極(図示ではS極
)位置に対向して配置することにより、トナ一層の厚さ
を薄< (30gm〜300g+* )且つ均一に規制
する。The non-magnetic cylinder 2, which is a developer carrier, rotates in the developing section so as to move in the same direction as the surface of the electrostatic image carrier. A multipolar permanent magnet 3 is arranged inside the nonmagnetic cylinder 2 so as not to rotate. The one-component insulating magnetic developer 6 sent from the developer container 4 is applied onto the non-magnetic cylindrical surface, and the friction between the cylindrical surface and the toner particles imparts a charge of opposite polarity to the electrostatic image charge to the toner particles. give. Furthermore, an iron doctor blade 5 is placed close to the cylindrical surface (at intervals of 50μ11 to 500μ).
+*), by arranging it to face one magnetic pole (the S pole in the figure) of the multipolar permanent magnet 3, thereby regulating the thickness of one layer of the toner to be thin (30 gm to 300 g+*) and uniform.
この円筒2の回転速度を調節することにより、現像剤層
の表層速度及び好ましくは内部速度が静電像保持面の速
度と実質的に等速、もしくはそれに近い速度となるよう
にする。ドクターブレード5として鉄のかわりに永久磁
石を用いて対向磁極を形成してもよい、また、現像部に
おいて現像剤担体と静電像保持面との間で交流バイアス
を印加してもよい、この交流バイアスはfが200〜4
000Hz、 Vppが500〜3000Vテあれば良
い。By adjusting the rotational speed of the cylinder 2, the surface speed and preferably the internal speed of the developer layer are made to be substantially equal to or close to the speed of the electrostatic image holding surface. A permanent magnet may be used instead of iron as the doctor blade 5 to form opposing magnetic poles, and an alternating current bias may be applied between the developer carrier and the electrostatic image holding surface in the developing section. AC bias f is 200~4
000Hz and Vpp of 500 to 3000V are sufficient.
以上の如く、この現像工程においては一成分系磁性現像
剤を現像剤担体上に安定に保持させる為に、多極永久磁
石3を内包する非磁性円筒2を用いた。また、現像剤層
を薄く均一に形成する為に、円筒2表面に近接して磁性
体薄板もしくは永久磁石によるドクターブレード5を配
置した。このように磁性体のドクターブレードを用いる
と。As described above, in this developing step, the non-magnetic cylinder 2 containing the multipolar permanent magnet 3 was used in order to stably hold the one-component magnetic developer on the developer carrier. In addition, in order to form a thin and uniform developer layer, a doctor blade 5 made of a magnetic thin plate or a permanent magnet was placed close to the surface of the cylinder 2. Using a magnetic doctor blade like this.
現像剤担体に内包された永久磁石の磁極との間に対向磁
極が形成され、ドクターブレードと現像剤担体間でトナ
ー粒子類を強制的に立ち上がらせることになり、現像剤
担体上の他の部分、例えば静電像面に相対する現像部分
の現像剤層を薄く規制するのに有利である。さらにその
ような強制的運動を現像剤に与えることにより現像剤層
はより均一になり、薄く且つ均一なトナ一層形成が達せ
られる。しかもドクターブレードとスリーブとの間隔を
広めに設定できるからトナー粒子の破壊やa集を防止す
る効果もある。現像部分におけるトナー粒子の転移に際
し、静電像の吸引作用あるいは交流バイアスの作用によ
って静電像側に転移する。Opposing magnetic poles are formed between the magnetic poles of the permanent magnet contained in the developer carrier, and the toner particles are forcibly raised between the doctor blade and the developer carrier, causing the toner particles to stand up on other parts of the developer carrier. This is advantageous, for example, in controlling the thickness of the developer layer in the development area facing the electrostatic image surface. Further, by imparting such forced movement to the developer, the developer layer becomes more uniform and a thin and uniform toner layer formation is achieved. Moreover, since the distance between the doctor blade and the sleeve can be set wide, there is an effect of preventing the destruction of toner particles and agglomeration. When the toner particles are transferred in the developing area, they are transferred to the electrostatic image side due to the attraction action of the electrostatic image or the action of an alternating current bias.
この静電像保持体である感光ドラム上の静電潜像を可視
像にする現像工程で、感光体の明部(光が当った部分)
にトナーが余分に付着して、カブリが発生するのを防止
するため、現像スリーブに感光ドラムの明部電位VLよ
り高い一定の直流バイアスVOCを印加させる。In the development process, the electrostatic latent image on the photosensitive drum, which is an electrostatic image holder, is turned into a visible image.
In order to prevent excess toner from adhering to the photosensitive drum and causing fog, a constant DC bias VOC higher than the bright area potential VL of the photosensitive drum is applied to the developing sleeve.
さらに、多重・多色コピーなどのための指足区分の画像
消去を行なうため、LED、ヒユーズランプ等で、トラ
ム電位がそれ以上下がらないくらいの強い光を当て、明
部電位VSt を感光体に与える。Furthermore, in order to erase the image of finger and toe divisions for multiplex/multicolor copying, etc., a strong light such as an LED or a fuse lamp is applied to prevent the tram potential from decreasing further, and the bright area potential VSt is applied to the photoreceptor. give.
しかしながら、感光体上にフィルミングが発生すると、
本来の光量が感光体に当たらず、コントラストが低下し
、カブリが発生する。However, when filming occurs on the photoreceptor,
The original amount of light does not hit the photoreceptor, resulting in decreased contrast and fog.
この様な現象を排除することが必要であり、それに極め
て有効な方法を本発明者らは、見い出すに至った。It is necessary to eliminate such a phenomenon, and the present inventors have discovered a method that is extremely effective for this purpose.
[発明が解決しようとする問題点]
本発明の目的は、上述の問題点を解決した現像剤を提供
することにある。[Problems to be Solved by the Invention] An object of the present invention is to provide a developer that solves the above-mentioned problems.
すなわち、本発明の目的は、フィルミングによるカブリ
のない現像剤を提供することにある。That is, an object of the present invention is to provide a developer that is free from fog due to filming.
本発明の更なる目的は感光体クリーナ一部への過多のシ
リカ蓄積をなくし、感光体を傷つけることを防止する現
像剤の製造方法を提供することにある。A further object of the present invention is to provide a method for producing a developer that eliminates excessive silica accumulation on a portion of a photoreceptor cleaner and prevents damage to the photoreceptor.
本発明の他の目的は、多色・多重コピーにおいても色の
混在の発生しない現像剤の製造方法を提供することにあ
る。Another object of the present invention is to provide a method for producing a developer that does not cause mixing of colors even in multicolor/multiple copying.
また、本発明の他の目的はトナー消費量の少ない現像剤
の製造方法を提供することにある。Another object of the present invention is to provide a method for producing a developer that consumes less toner.
C問題点を解決するための手段および作用]本発明では
、ケイ酸微粉末が添加された電子写真用現像剤において
、トナーに未付着のケイ酸微粉末を除去することによっ
て上記目的を達成するものである。Means and operation for solving problem C] In the present invention, in an electrophotographic developer to which fine silicic acid powder is added, the above object is achieved by removing fine silicic acid powder that is not attached to the toner. It is something.
本発明で用いるケイ酸微粉末とは、5i−0−Si結合
を有する微粉体であって、乾式法で製造されたもの、及
び湿式法で製造されたもののいずれも含まれる。The silicic acid fine powder used in the present invention is a fine powder having a 5i-0-Si bond, and includes both those manufactured by a dry method and those manufactured by a wet method.
本発明に用いられるケイ酸微粉体を湿式法で製造する方
法は、従来公知である種々の方法が適用できる。たとえ
ば、ケイ酸ナトリウムの酸による分解、一般反応式で示
せば(以下反応式は略す)、
Na20−xsi02+Hci)+H20+ 5i
02−nH20争Nac#その他、ケイ酸ナトリウムの
アンモニア塩類またはアルカリ塩類による分解、ケイ酸
ナトリウムよりアルカリ土類金属ケイ酸塩を生成せしめ
た後。Various conventionally known methods can be applied to produce the silicic acid fine powder used in the present invention by a wet method. For example, the decomposition of sodium silicate with an acid can be expressed by the general reaction formula (the reaction formula is omitted below): Na20-xsi02+Hci)+H20+ 5i
02-nH20 Nac #Other decomposition of sodium silicate with ammonia salts or alkali salts, after producing alkaline earth metal silicate from sodium silicate.
酸で分解しケイ酸とする方法、ケイ酸ナトリウム溶液を
イオン交換樹脂によりケイ酸とする方法。A method of decomposing with an acid to form silicic acid, and a method of converting a sodium silicate solution to silicic acid using an ion exchange resin.
天然ケイ酸またはケイ酸塩を利用する方法などがある。There are methods that use natural silicic acid or silicates.
ここでいうケイ酸微粉体には、無水−酸化ケイ素(シリ
カ)の他、ケイ酸アルミニウム、ケイ酸ナトリウム、ケ
イ酸カリウム、ケイ酸マグネシウム、ケイ酸亜鉛などの
ケイ酸塩をいずれも適用できる。また、これらのケイ酸
微粉体の適用績は現像剤重量に対して、0.01〜6重
量%の時に効果を発揮し、好ましくは0.02〜3重量
%、特に好ましくは0.05〜1重量%添加した際に優
れた安定性を示す、添加形態について好ましい態様を述
べれば、現像剤重量に対して0.01〜!重量%のケイ
酸微粉体がトナー粒子表面に付着している状態にあるの
が良い。In addition to anhydrous silicon oxide (silica), silicates such as aluminum silicate, sodium silicate, potassium silicate, magnesium silicate, and zinc silicate can be used as the silicic acid fine powder here. In addition, these silicic acid fine powders are effective when applied in an amount of 0.01 to 6% by weight, preferably 0.02 to 3% by weight, particularly preferably 0.05 to 6% by weight, based on the weight of the developer. A preferred form of addition that exhibits excellent stability when added at 1% by weight is 0.01 to 0.01% by weight of the developer! It is preferable that % by weight of the fine silicic acid powder be attached to the surface of the toner particles.
遊離シリカを除去する方法としては、風力分級a等を用
いて、分級によって遊離シリカを除去することが最も有
効な方法である。The most effective method for removing free silica is to remove free silica by classification using air classification a or the like.
本発明に用いるトナーとしては、粉砕工程を経たトナー
、マイクロカプセル化されたトナー、懸1ftm合によ
り形成されたトナーのいずれでも良い、粉砕工程を経た
トナーにおいては、トナーを所定粒度(例えば、体積平
均粒径1〜20gm)に分級後1分級法トナーとソリ力
を混合してシリカを外添し、その後分級によって遊離シ
リカを除去するのが好ましい。The toner used in the present invention may be a toner that has undergone a pulverization process, a micro-encapsulated toner, or a toner formed by 1 ftm suspension. It is preferable that silica is externally added by mixing the classified toner and the warp force after classification to an average particle size of 1 to 20 gm, and then free silica is removed by classification.
本発明に使用するトナーの結着樹脂としては、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の置換体の単重合体;スチレン−p
−クロルスチレン共重合体、スチレン−プロピレン共重
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−アクリル酸メチ
ル共重合体、スチレン−アクリル酸エチル共重合体、ス
チレンーアクリル酸ブチル共重合体、スチレン−アクリ
ル酸・2工チルヘキシル共重合体、スチレン−アクリル
酸オクチル共重合体、スチレン−メタアクリル酸メチル
共重合体、スチレン−メタアクリル酸エチル共重合体、
スチレン−メタアクリル酸ブチル共重合体、スチレン−
αクロルメタアクリル酸メチル共重合体、スチレン−ア
クリロニトリル共ffi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
重合体、スチレン−ビニルメチルケトン共重合体、スチ
レン−ブタジェン共重合体、スチレン−イソプレン共重
合体、スチレン−アクリロニトリル−インデン共重合体
、スチレン−マレイン酸共重合体、スチレン−マレイン
酸エステル共用合体などのスチレン系共重合体;ポリメ
チルメタクリレート、ポリブチルメタクリレート、ポリ
塩化ビニル、ポリ酢酸ビニル、ポリエチレン、ポリプロ
ピレン、ポリエステル、ポリウレタン、ポリアミド、エ
ポキシ樹脂、ポリビニルブチラール、ポリアマイド、ポ
リアクリル酸樹脂、ロジン、変性ロジン、テルペン樹脂
、フェノール樹脂、脂肪族又は脂環族炭化水素樹脂、芳
香族系石油樹脂、塩素化パラフィン、パラフィンワック
ス、カルナ八ワックスなどが単独或いは混合して使用で
きる。As the binder resin of the toner used in the present invention, monopolymers of styrene and its substituted products such as polystyrene, polyP-chlorostyrene, and polyvinyltoluene;
-Chlorstyrene copolymer, styrene-propylene copolymer, styrene-vinyltoluene copolymer, styrene-
Vinylnaphthalene copolymer, styrene-methyl acrylate copolymer, styrene-ethyl acrylate copolymer, styrene-butyl acrylate copolymer, styrene-acrylic acid/2-functional tylhexyl copolymer, styrene-octyl acrylate copolymer, styrene-methyl methacrylate copolymer, styrene-ethyl methacrylate copolymer,
Styrene-butyl methacrylate copolymer, styrene-
α-chloromethyl methacrylate copolymer, styrene-acrylonitrile co-ffi copolymer, styrene-vinyl methyl ether copolymer, styrene-vinylethyl ether copolymer, styrene-vinyl methyl ketone copolymer, styrene-butadiene copolymer , styrene-based copolymers such as styrene-isoprene copolymer, styrene-acrylonitrile-indene copolymer, styrene-maleic acid copolymer, and styrene-maleic acid ester copolymer; polymethyl methacrylate, polybutyl methacrylate, polychloride Vinyl, polyvinyl acetate, polyethylene, polypropylene, polyester, polyurethane, polyamide, epoxy resin, polyvinyl butyral, polyamide, polyacrylic acid resin, rosin, modified rosin, terpene resin, phenolic resin, aliphatic or alicyclic hydrocarbon resin, Aromatic petroleum resins, chlorinated paraffin, paraffin wax, caruna wax, etc. can be used alone or in combination.
必要に応じて、本発明に使用するトナーに用いる着色材
料としては、従来公知のカーボンブラック、銅フタロシ
アニン鉄黒などが使用でき、従来公知の正あるいは負の
荷電制御剤が本発明に用いられる。If necessary, conventionally known carbon black, copper phthalocyanine iron black, etc. can be used as the coloring material used in the toner used in the present invention, and conventionally known positive or negative charge control agents can be used in the present invention.
さらに本発明のトナーには必要に応じ・て、簡滑剤、導
電性付与剤、定着助剤などの例えば、ポリテトラフルオ
ロエチレン粉、ポリフッ化ビニリデン粉、高級脂肪酸の
金属塩、カーボンブラック、導電性酸化錫、などが添加
されても良い。Furthermore, the toner of the present invention may optionally contain lubricants, conductivity imparting agents, fixing aids, etc., such as polytetrafluoroethylene powder, polyvinylidene fluoride powder, metal salts of higher fatty acids, carbon black, and conductive agents. Tin oxide, etc. may be added.
さらに本発明のトナーは体積固有抵抗がlQi 000
11以上、特に10】2Ωca+以上であるのが良い。Further, the toner of the present invention has a volume resistivity of lQi 000
It is preferably 11 or more, particularly 10]2 Ωca+ or more.
ここで言う体積固有抵抗は、トナーを100 kg/c
m2の圧で成型し、これに100 V/c+sの電界を
印加して、印加後1分を経た後の電流値から換算した値
として定義される。The volume resistivity mentioned here is 100 kg/c of toner.
It is defined as the value calculated from the current value after 1 minute has elapsed after molding with a pressure of m2 and applying an electric field of 100 V/c+s.
本発明のトナーは、必要に応じて、鉄粉、ガラスピーズ
、ニッケル粉、フェライト粉などのキャリヤー粒子と混
合され、電気的潜像の現像剤として用いることもできる
。The toner of the present invention can also be mixed with carrier particles such as iron powder, glass beads, nickel powder, ferrite powder, etc., if necessary, and used as a developer for electrical latent images.
また、本発明には必要に応じて磁性粉を含有してもよい
、その磁性粉としては磁場の中に置かれて磁化される物
質が用いられ、鉄、コバルト、ニッケルなどの強磁性金
属の粉末もしくはマグネタイト、γ−Fe+03. フ
ェライトなどの合金や化合物がある。Furthermore, the present invention may contain magnetic powder if necessary. The magnetic powder is a substance that is magnetized when placed in a magnetic field, and is made of ferromagnetic metals such as iron, cobalt, and nickel. Powder or magnetite, γ-Fe+03. There are alloys and compounds such as ferrite.
特に前述の効果を発揮せしめるためには好ましくは窒素
吸着法によるBET比表面植が2〜20m2/g、特に
2,5〜12II2/gの磁性粉が好ましい。In particular, in order to exhibit the above-mentioned effects, magnetic powder with a BET specific surface density of 2 to 20 m2/g, particularly 2.5 to 12 II2/g, determined by the nitrogen adsorption method is preferred.
この磁性粉の含有量はトナー重量に対して10〜70重
量%が良い。The content of this magnetic powder is preferably 10 to 70% by weight based on the weight of the toner.
[実施例]
以上本発明の基本的な構成と特色について述べたが、以
下実施例にもとづいて具体的に本発明の方法について説
明する。しかしながら、これによって本発明の実施の態
様がなんら限定されるものではない。実施例中の部数は
重量部である。[Example] The basic structure and features of the present invention have been described above, and the method of the present invention will be specifically explained based on Examples below. However, this does not limit the embodiments of the present invention in any way. Parts in the examples are parts by weight.
実施例1
スチレン−2エチルへキシルアクリレート−ジビニルベ
ンゼン共重合体100部、ニグロシン4部、BET比表
面桔8rrr27gのマグネタイト50部を混合し、ロ
ールミルにて、160℃で、溶融混練する。冷却後、ハ
ンマーミルにて、粗粉砕した後、ジェy )粉砕機にて
微粉砕する。次いで風力分級機を用いて分級し、体積平
均径がおよそ11μmの黒色粉体を得た。Example 1 100 parts of styrene-2-ethylhexyl acrylate-divinylbenzene copolymer, 4 parts of nigrosine, and 50 parts of magnetite having a BET specific surface area of 8 rrr27 g were mixed and melt-kneaded at 160°C in a roll mill. After cooling, the mixture is coarsely pulverized using a hammer mill, and then finely pulverized using a pulverizer. Next, it was classified using an air classifier to obtain a black powder having a volume average diameter of approximately 11 μm.
この黒色粉体に、ケイ酸微粉末を0.5重量%添加し、
ヘンシェルミキサーで混合し、さらに風力分級機を用い
て未付着のケイ酸微粉末を除去することによりケイ酸微
粉末含有量が0.4重量%の現像剤を得た。Adding 0.5% by weight of silicic acid fine powder to this black powder,
A developer having a silicic acid fine powder content of 0.4% by weight was obtained by mixing with a Henschel mixer and removing unattached fine silicic acid powder using an air classifier.
次いでOPC感光体に負の静電荷像を形成させ、上記の
現像剤を用いて、前述の方法によって現像、さらに転写
、定着させたところ3万枚コピー後も得られた画像は濃
度1.22と高く、フィルミングによるカブリもなく、
鮮明な画像が得られた。Next, a negative electrostatic image was formed on the OPC photoreceptor, and the image was developed using the above-mentioned developer and transferred and fixed using the method described above. Even after copying 30,000 copies, the resulting image had a density of 1.22. and there is no fog due to filming.
A clear image was obtained.
実施例2
実施例1の黒色粉体にケイ酸微粉末を0.7重量%添加
した後実施例1と同様にして現像剤を得た。Example 2 After adding 0.7% by weight of silicic acid fine powder to the black powder of Example 1, a developer was obtained in the same manner as in Example 1.
実施例1と同様にテストを行なったところ、濃度は1.
20と高く、フィルミングによるカブリも全くなかった
。When a test was conducted in the same manner as in Example 1, the concentration was 1.
20, and there was no fog due to filming at all.
比較例1
実施例1の黒色粉体に、ケイ酸微粉末を0.4重量%添
加して、ヘンシェルミキサーで混合し、未付着のケイ酸
微粉末の除去のための分級を行なわずに現像剤とした。Comparative Example 1 0.4% by weight of silicic acid fine powder was added to the black powder of Example 1, mixed in a Henschel mixer, and developed without performing classification to remove unattached silicic acid fine powder. It was used as a drug.
これを、実施例1と同様にテストを行なったところ、2
千枚コピー後に感光体上にフィルミングが発生し、それ
によるカブリが発生した。When this was tested in the same manner as in Example 1, 2
After copying 1,000 copies, filming occurred on the photoreceptor, resulting in fogging.
[発明の効果]
以上のように、本発明の製造方法で得られる電子写真用
現像剤はM離シリカを実質的に含まないため、感光体上
へのmfllシリカの付着を原因とするフィルミングを
防止でき、カブリのない画像が得られ、また、感光体ク
リーナ部への過多なシリカ蓄積がないため感光体を傷つ
けることも防止でき、感光体の耐久性も良好で、長期に
わたって良好な画像が得られる。また、多色・多重コピ
ーにおいても色が混存しない、更にはトナー消費量も少
なくなる。[Effects of the Invention] As described above, since the electrophotographic developer obtained by the production method of the present invention does not substantially contain M-releasing silica, it is free from filming caused by adhesion of MFLl silica onto the photoreceptor. In addition, there is no excessive silica accumulation on the photoconductor cleaner area, which prevents damage to the photoconductor, and the photoconductor has good durability, resulting in good images over a long period of time. is obtained. Furthermore, even in multicolor/multiple copies, colors do not mix, and toner consumption is reduced.
第1図は本発明を適用できる現像工程の一実施形態の説
明図である。
1:静電像保持体
2:現像剤担体
3:永久磁石
4:現像剤容器
5:ドクターブレード
6:現像剤FIG. 1 is an explanatory diagram of one embodiment of a developing process to which the present invention can be applied. 1: Electrostatic image holder 2: Developer carrier 3: Permanent magnet 4: Developer container 5: Doctor blade 6: Developer
Claims (1)
において、トナーに未付着のケイ酸微粉末を除去するこ
とを特徴とする電子写真用現像剤の製造方法。A method for producing an electrophotographic developer to which fine silicic acid powder is added, the method comprising removing the fine silicic acid powder not attached to the toner.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61148090A JPH083651B2 (en) | 1986-06-26 | 1986-06-26 | Method for producing electrophotographic developer |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61148090A JPH083651B2 (en) | 1986-06-26 | 1986-06-26 | Method for producing electrophotographic developer |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63139366A true JPS63139366A (en) | 1988-06-11 |
JPH083651B2 JPH083651B2 (en) | 1996-01-17 |
Family
ID=15445013
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61148090A Expired - Fee Related JPH083651B2 (en) | 1986-06-26 | 1986-06-26 | Method for producing electrophotographic developer |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH083651B2 (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2635882A1 (en) * | 1988-08-31 | 1990-03-02 | Canon Kk | ELECTROSTATIC IMAGE DEVELOPER |
JPH0291660A (en) * | 1988-09-28 | 1990-03-30 | Tdk Corp | Production of toner for electrophotography and electrophotographic developing method |
US5202213A (en) * | 1988-08-31 | 1993-04-13 | Canon Kabushiki Kaisha | Developer with surface treated silicic acid for developing electrostatic image |
US6677096B2 (en) | 2001-04-27 | 2004-01-13 | Kao Corporation | Positively chargeable toner for two-component development |
US7011921B2 (en) | 2002-08-12 | 2006-03-14 | Ricoh Company, Ltd. | Method and apparatus for producing toner for electrophotography |
JP2007086348A (en) * | 2005-09-21 | 2007-04-05 | Fuji Xerox Co Ltd | Method for manufacturing electrophotographic toner |
US8703378B2 (en) | 2010-09-16 | 2014-04-22 | Ricoh Company, Ltd. | Method of manufacturing toner and toner manufactured by the method |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5358244A (en) * | 1976-11-08 | 1978-05-26 | Konishiroku Photo Ind Co Ltd | Preparation of electrostatic image developer |
-
1986
- 1986-06-26 JP JP61148090A patent/JPH083651B2/en not_active Expired - Fee Related
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5358244A (en) * | 1976-11-08 | 1978-05-26 | Konishiroku Photo Ind Co Ltd | Preparation of electrostatic image developer |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2635882A1 (en) * | 1988-08-31 | 1990-03-02 | Canon Kk | ELECTROSTATIC IMAGE DEVELOPER |
US5202213A (en) * | 1988-08-31 | 1993-04-13 | Canon Kabushiki Kaisha | Developer with surface treated silicic acid for developing electrostatic image |
JPH0291660A (en) * | 1988-09-28 | 1990-03-30 | Tdk Corp | Production of toner for electrophotography and electrophotographic developing method |
US6677096B2 (en) | 2001-04-27 | 2004-01-13 | Kao Corporation | Positively chargeable toner for two-component development |
US7011921B2 (en) | 2002-08-12 | 2006-03-14 | Ricoh Company, Ltd. | Method and apparatus for producing toner for electrophotography |
JP2007086348A (en) * | 2005-09-21 | 2007-04-05 | Fuji Xerox Co Ltd | Method for manufacturing electrophotographic toner |
JP4661488B2 (en) * | 2005-09-21 | 2011-03-30 | 富士ゼロックス株式会社 | Electrophotographic toner manufacturing equipment |
US8703378B2 (en) | 2010-09-16 | 2014-04-22 | Ricoh Company, Ltd. | Method of manufacturing toner and toner manufactured by the method |
Also Published As
Publication number | Publication date |
---|---|
JPH083651B2 (en) | 1996-01-17 |
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