JPH01126670A - Electrophotographic image producing method - Google Patents
Electrophotographic image producing methodInfo
- Publication number
- JPH01126670A JPH01126670A JP28459487A JP28459487A JPH01126670A JP H01126670 A JPH01126670 A JP H01126670A JP 28459487 A JP28459487 A JP 28459487A JP 28459487 A JP28459487 A JP 28459487A JP H01126670 A JPH01126670 A JP H01126670A
- Authority
- JP
- Japan
- Prior art keywords
- toner
- cleaning
- particles
- developing device
- undefined
- 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
- 238000000034 method Methods 0.000 title claims abstract description 24
- 239000002245 particle Substances 0.000 claims abstract description 49
- 108091008695 photoreceptors Proteins 0.000 claims description 20
- 238000004140 cleaning Methods 0.000 abstract description 39
- 239000000969 carrier Substances 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 description 20
- 230000005291 magnetic effect Effects 0.000 description 11
- 229920005989 resin Polymers 0.000 description 11
- 239000011347 resin Substances 0.000 description 11
- 239000000203 mixture Substances 0.000 description 9
- 230000007547 defect Effects 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 229920000642 polymer Polymers 0.000 description 7
- 239000000126 substance Substances 0.000 description 6
- 239000006229 carbon black Substances 0.000 description 5
- 239000000975 dye Substances 0.000 description 5
- 230000009477 glass transition Effects 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- -1 polyethylene Polymers 0.000 description 5
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000003086 colorant Substances 0.000 description 4
- 239000006247 magnetic powder Substances 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 239000012798 spherical particle Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 229910000859 α-Fe Inorganic materials 0.000 description 3
- LRFVTYWOQMYALW-UHFFFAOYSA-N 9H-xanthine Chemical compound O=C1NC(=O)NC2=C1NC=N2 LRFVTYWOQMYALW-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 210000005069 ears Anatomy 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000000696 magnetic material Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 239000012860 organic pigment Substances 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 1
- VBHXIMACZBQHPX-UHFFFAOYSA-N 2,2,2-trifluoroethyl prop-2-enoate Chemical compound FC(F)(F)COC(=O)C=C VBHXIMACZBQHPX-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 102100022587 Peroxisomal multifunctional enzyme type 2 Human genes 0.000 description 1
- 101710125609 Peroxisomal multifunctional enzyme type 2 Proteins 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- 241000978776 Senegalia senegal Species 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 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
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 229910052790 beryllium Inorganic materials 0.000 description 1
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- DFYKHEXCUQCPEB-UHFFFAOYSA-N butyl 2-methylprop-2-enoate;styrene Chemical compound C=CC1=CC=CC=C1.CCCCOC(=O)C(C)=C DFYKHEXCUQCPEB-UHFFFAOYSA-N 0.000 description 1
- 210000000078 claw Anatomy 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000011162 core material Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 210000003746 feather Anatomy 0.000 description 1
- 230000005294 ferromagnetic effect Effects 0.000 description 1
- 239000010419 fine particle 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
- 229910052742 iron Inorganic materials 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
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 229920005672 polyolefin resin 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
- 239000000843 powder Substances 0.000 description 1
- 239000011164 primary particle Substances 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 230000007704 transition Effects 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
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 1
- 229940075420 xanthine Drugs 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Landscapes
- Cleaning In Electrography (AREA)
Abstract
Description
微粟其へ帆叩褒吐
本発明は一成分または二成分現像剤による電子写真方式
の複写機およびプリンターに用いられる作像方法に関す
る。
従来の技術
電子写真方式の複写機、あるいはプリンターにより画像
を得るには、まず画像担体である感光体の表面に静電潜
像を形成する。つぎに、この静電潜像を有する感光体表
面を現像剤を用いて現像し、得られたトナー像を紙など
に転写する。
かかる電子写真複写機等に用いられる現像剤には、主と
して絶縁性非磁性トナーおよび磁性キャリアからなる二
成分系現像剤と、磁性体を含有する絶縁性磁性トナーの
みからなる一成分系現像剤、あるいは非磁性トナーによ
る一成分系現像剤とがある。このようなトナーは通常熱
可塑性樹脂、着色剤、荷電制御剤、さらに磁性トナーの
場合は磁性粉などからなっている。
近年、このような電子写真において画像の高精細を目的
にトナーの小径化が検討されている。しかしながら、こ
のような小径粒子は流動性が悪く、また現像後の感光体
のクリーニング不良を生ずる。
クリーニングは、感光体に付着したトナーのうち紙に転
写されなかった残留トナーをゴムなどのブレードで感光
体表面より除去するものであり、かかるクリーニングが
充分でないと次回の良好な画像形成ができない。
また、帯電量の安定化、流動性向上のためトナーの形状
を球形化することも検討されている。しかし、かかる球
形粒子もクリーニング性を大きく悪化させるという欠点
がある。
発明が解決しようとする問題点
このようなりリーニング不良を解決するものとして、球
形トナーとこれよりも平均粒径の小さな不定形トナーと
の混合トナーを用いることが提案されている(特開昭5
9−102252号参照)。しかしながら、かかる提案
では球形トナーによる優れた高流動性、緻密な潜像現像
特性等の効果が減殺される。
ゝ・
本発明は、球船のトナーを用いて高精細、緻密な画像を
得つつ、クリーニング性に優れた電子写真現像法を提供
するものである。
濁題点を 決するための
すなわち、本発明は、球形トナーを使用する電子写真現
像方法において、転写後に感光体表面を不定形の粒子に
より現像操作を行い、その後感光体のクリーニングを行
うことを特徴とする電子写真作像方法を提供するもので
ある。
寒監鳳
つぎに本発明を実施例によりさらに具体的に説明する。
第1図は本発明の作像方法を実施する現像装置を示す概
略断面図である。第1図において、現像装置lは、感光
体ドラム(10)の周囲にメインチャージャー(11)
、露光装置(12)、球形トナーを用いた主現像装置(
13)、転写チャージャー(16)、不定形トナーを用
いたクリーニング用現像装置(17)、クリーニングブ
レード(18)、イレーサランブ(19)が設けられ、
感光体ドラム(10)が矢印方向に一回転する間に、帯
電−露光−球形トナーによる現像−転写−不定形トナー
による現像−クリーニングの各工程を行うものである。
したがって、作像プロセスは、つぎの(a)〜(g)の
工程に従い行われる。
(a)感光体ドラム(10)の表面をメインチャージャ
ー(11)で均一に帯電する。
(b)つぎに該感光体にレーザビーム(12)等を照射
して露光を行い静電潜像を形成する。
(c)つぎに主現像装置(13)により現像を行う。現
像剤は球形トナーとキャリアーを含む2成分系磁性現像
剤を用いる。球形トナーはホッパーから現像装置内に運
ばれ、撹拌羽根(20)によってキャリアと充分に混合
され所望の帯電量を得る。該球形トナーは現像スリーブ
(21)上のキャリアの穂によって運ばれ感光体ドラム
(10)の静電潜像上に移動し現像が行われる。なお、
感光体の残留電位を考慮して現像スリーブ(21)にバ
イアス電圧を印加してもよい。
(d)得られたトナー画像を転写チャージャー(16)
を用いて紙等の記録保持体上に転写、定着する。紙は給
紙ローラー(22)から供給され転写後、分離爪(23
)により感光体ドラム(10)より分離され搬送ベルト
(24)により装置外部に取り出される。
(e)クリーニング用現像装置(17)により現像を行
う。現像剤は球形でないいわゆる不定形トナーなどの不
定形粒子とキャリアーを含む2成分系現像剤を用いる。
不定形粒子は現像装置内にて撹拌羽根(25)によって
キャリアと充分に混合され所望の帯電量を得る。該不定
形粒子は現像スリーブ(26)上のキャリアの穂によっ
て運ばれ感光体(10)と現像スリーブ(26)との間
に印加されたバイアス電圧によって現像が行われる。該
バイアス電圧は感光体の特性、不定形粒子の帯電特性な
どのプロセス条件により適宜選択される。
(f)クリーニングブレード(18)により感光体ドラ
ム(10)表面の残留トナーが掻き落とされる。
(g)イレーサーランプ(19)により感光体の表面電
位がOV近くまで落とされ、引き続き帯電、潜像形成に
供される。
本発明方法に用いられる前記球形トナーはバインダー樹
脂、着色剤、荷電制御剤、磁性体、その他公知のトナー
成分からなる。また、不定形粒子として用いられる不定
形トナーも該球形トナーと同様の成分からなってよい。
さらに不定形粒子としては、着色剤を含まず前記バイン
ダー樹脂のみを適宜の方法により粉砕して得られたもの
であってもよい。
球形トナーは、不定形のトナー粒子を飛散させ熱風で処
理して球形化する方法、トナー成分を分散混合した樹脂
溶液を噴霧乾燥させるスプレードライ法、トナー成分を
分散混合したしたモノマーよりなる分散液より懸濁重合
を行う方法により製造することができる。
該球形トナーの粒径は3〜20μlであるのが好ましい
。粒径が3μ肩より小さいと画像濃度が低下する。一方
20μ友より大きいと画質が粗くなる。
一方、本発明方法に用いられる不定形トナーは、例えば
、前記材料をミキサーなどにより充分混合した後、押出
し混練機を用いて、溶融、混練して得られる従来公知の
不定形の形状をなすトナーであってよい。得られた混線
物を冷却後、微粉砕して分級し、5〜20μ肩の所定の
粒径を有するトナーを得る。
なお、不定形粒子の平均粒径は球形トナーの粒径より小
さいことが望ましい。球形トナーと同等以上の粒径を有
するトナーであっても使用できるが、ブレードと感光体
の間に不定形トナーが挿入された場合不定形トナーの粒
径が小さいほうが球形トナーの擦り抜けを防止できる。
さらに、球形トナーと反対極性に帯電する不定形粒子を
用いると、残留した球形トナーと不定形トナーが静電的
に吸着し大きな粒子となってよりクリーニングしやすく
なり好ましい。
これら球形および不定形トナーのバインダー樹脂として
は、ポリスチレン、スチレンアクリル共重合体、ポリエ
ステル、エポキシ樹脂、ポリエチレン、ポリプロピレン
などのポリオレフィン樹脂、ポリアミド樹脂、マレイン
酸樹脂、あるいはこれらの変性樹脂などの従来公知の樹
脂が挙げられる。
これらは、単独、または2種以上を混合してもよい。
また、着色剤としては、カーボンブラック、フタロシア
ニン系、キサンチン系の有機顔料および染料などが用い
られる。
その他必要によりニグロシン系染料、トリフェニールメ
タン系染料などの荷電制御剤シリカ、酸化チタン、フッ
化ビニリデンなどの流動化剤、あるいはポリプロピレン
、ポリエチレンなどの離型剤等、公知の添加剤を配合し
てもよい。
また、トナーのみからなる一成分系磁性現像剤の場合、
磁性トナーに配合される磁性材料としては、例えば、鉄
、ニッケル、コバルト等の金属、これらの金属と亜鉛、
アンチモン、アルミニウム、鉛、スズ、ビスマス、ベリ
リウム、マンガン、セレン、タングステン、ジルコニウ
ム、バナジウム等の金属との合金あるいは混合物、酸化
鉄、酸化チタン、酸化マグネシウム等の金属酸化物との
混合物および強磁性フェライト、マグネタイト、並びに
これらの混合物等が挙げられる。
これら磁性体の粒径は一次粒子として2μ肩以下、好ま
しくは1μl以下である。また、前記ポリマーと磁性粉
との配合割合は、樹脂100重量部に対して磁性粉10
0〜900重量部、好ましくは200〜800重蛍部で
ある。
寒監外
以下に、製造例、実施例および比較例に基づき本発明を
さらに詳しく説明する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an image forming method used in electrophotographic copying machines and printers using a one-component or two-component developer. 2. Description of the Related Art In order to obtain an image using an electrophotographic copying machine or printer, an electrostatic latent image is first formed on the surface of a photoreceptor, which is an image carrier. Next, the surface of the photoreceptor having this electrostatic latent image is developed using a developer, and the resulting toner image is transferred onto paper or the like. Developers used in such electrophotographic copying machines include a two-component developer mainly consisting of an insulating non-magnetic toner and a magnetic carrier, a one-component developer consisting only of an insulating magnetic toner containing a magnetic substance, Alternatively, there is a one-component developer using non-magnetic toner. Such toner usually comprises a thermoplastic resin, a colorant, a charge control agent, and, in the case of a magnetic toner, magnetic powder. In recent years, in such electrophotography, efforts have been made to reduce the diameter of toner for the purpose of achieving high definition images. However, such small-diameter particles have poor fluidity and also cause poor cleaning of the photoreceptor after development. Cleaning involves removing residual toner that has not been transferred to the paper from the surface of the photoreceptor with a blade made of rubber or the like, and if such cleaning is not sufficient, it will not be possible to form a good image the next time. Further, in order to stabilize the amount of charge and improve fluidity, it is also being considered to make the toner spherical in shape. However, such spherical particles also have the disadvantage of greatly deteriorating cleaning performance. Problems to be Solved by the Invention In order to solve this problem of poor leaning, it has been proposed to use a mixed toner consisting of a spherical toner and an amorphous toner with a smaller average particle size (Japanese Patent Application Laid-Open No. 5-11112).
9-102252). However, in such a proposal, the effects of the spherical toner, such as excellent high fluidity and precise latent image development characteristics, are diminished.
ゝ- The present invention provides an electrophotographic developing method that uses spherical toner to obtain high-definition, precise images and has excellent cleaning properties. In order to solve the problem, the present invention is characterized in that, in an electrophotographic development method using spherical toner, the surface of the photoreceptor is developed with irregularly shaped particles after transfer, and then the photoreceptor is cleaned. The present invention provides an electrophotographic image forming method. Next, the present invention will be explained in more detail with reference to Examples. FIG. 1 is a schematic sectional view showing a developing device for carrying out the image forming method of the present invention. In FIG. 1, the developing device l includes a main charger (11) around a photoreceptor drum (10).
, exposure device (12), main developing device using spherical toner (
13), a transfer charger (16), a cleaning developing device (17) using irregularly shaped toner, a cleaning blade (18), and an eraser lamp (19),
While the photosensitive drum (10) rotates once in the direction of the arrow, the following steps are performed: charging, exposure, development with spherical toner, transfer, development with amorphous toner, and cleaning. Therefore, the image forming process is performed according to the following steps (a) to (g). (a) The surface of the photosensitive drum (10) is uniformly charged with the main charger (11). (b) Next, the photoreceptor is exposed to a laser beam (12) or the like to form an electrostatic latent image. (c) Next, the main developing device (13) performs development. A two-component magnetic developer containing spherical toner and carrier is used as the developer. The spherical toner is transported from the hopper into the developing device, and is sufficiently mixed with the carrier by a stirring blade (20) to obtain a desired amount of charge. The spherical toner is carried by the ears of carrier on the developing sleeve (21), moves onto the electrostatic latent image on the photosensitive drum (10), and is developed. In addition,
A bias voltage may be applied to the developing sleeve (21) in consideration of the residual potential of the photoreceptor. (d) Transfer the obtained toner image to a charger (16)
is used to transfer and fix the image onto a recording medium such as paper. The paper is fed from the paper feed roller (22), and after being transferred, the paper is moved to the separation claw (23).
) is separated from the photoreceptor drum (10) and taken out to the outside of the apparatus by a conveyor belt (24). (e) Developing is performed by the cleaning developing device (17). A two-component developer containing amorphous particles such as non-spherical toner and a carrier is used as the developer. The amorphous particles are sufficiently mixed with the carrier by a stirring blade (25) in the developing device to obtain a desired amount of charge. The irregularly shaped particles are carried by the ears of carrier on the developing sleeve (26) and are developed by a bias voltage applied between the photoreceptor (10) and the developing sleeve (26). The bias voltage is appropriately selected depending on process conditions such as the characteristics of the photoreceptor and the charging characteristics of the amorphous particles. (f) The residual toner on the surface of the photoreceptor drum (10) is scraped off by the cleaning blade (18). (g) The surface potential of the photoreceptor is lowered to near OV by the eraser lamp (19), and the photoreceptor is subsequently charged and used for forming a latent image. The spherical toner used in the method of the present invention comprises a binder resin, a colorant, a charge control agent, a magnetic material, and other known toner components. In addition, the amorphous toner used as the amorphous particles may also be composed of the same components as the spherical toner. Further, the amorphous particles may be obtained by pulverizing only the binder resin without containing a colorant by an appropriate method. Spherical toner can be produced by a method in which irregularly shaped toner particles are scattered and treated with hot air to make them spherical, a spray drying method in which a resin solution in which toner components are dispersed and mixed is spray-dried, and a dispersion made of monomers in which toner components are dispersed and mixed. It can be produced by a method of performing suspension polymerization. The particle size of the spherical toner is preferably 3 to 20 μl. When the particle size is smaller than 3 μm, image density decreases. On the other hand, if it is larger than 20μ, the image quality will be poor. On the other hand, the irregularly shaped toner used in the method of the present invention is, for example, a conventionally known irregularly shaped toner obtained by sufficiently mixing the above-mentioned materials using a mixer or the like, and then melting and kneading them using an extrusion kneader. It may be. After cooling the obtained mixed material, it is finely pulverized and classified to obtain a toner having a predetermined particle size of 5 to 20 μm. Note that it is desirable that the average particle size of the irregularly shaped particles is smaller than the particle size of the spherical toner. Although toner with a particle size equal to or larger than spherical toner can be used, if irregular-shaped toner is inserted between the blade and the photoconductor, a smaller particle size of irregular-shaped toner will prevent the spherical toner from slipping through. can. Furthermore, it is preferable to use amorphous particles that are charged to the opposite polarity to the spherical toner because the remaining spherical toner and amorphous toner are electrostatically attracted to each other and become large particles that are easier to clean. Binder resins for these spherical and amorphous toners include conventionally known binder resins such as polystyrene, styrene-acrylic copolymers, polyesters, epoxy resins, polyolefin resins such as polyethylene and polypropylene, polyamide resins, maleic acid resins, and modified resins thereof. Examples include resin. These may be used alone or in combination of two or more. Further, as the coloring agent, carbon black, phthalocyanine-based organic pigments, xanthine-based organic pigments, dyes, etc. are used. If necessary, other known additives may be added, such as charge control agents such as nigrosine dyes and triphenylmethane dyes, silica, fluidizing agents such as titanium oxide and vinylidene fluoride, and mold release agents such as polypropylene and polyethylene. Good too. In addition, in the case of a one-component magnetic developer consisting only of toner,
Examples of magnetic materials that can be mixed into magnetic toner include metals such as iron, nickel, and cobalt; these metals and zinc;
Alloys or mixtures with metals such as antimony, aluminum, lead, tin, bismuth, beryllium, manganese, selenium, tungsten, zirconium, vanadium, etc., mixtures with metal oxides such as iron oxide, titanium oxide, magnesium oxide, etc., and ferromagnetic ferrite. , magnetite, and mixtures thereof. The particle size of these magnetic substances is 2 μl or less, preferably 1 μl or less as a primary particle. The blending ratio of the polymer and magnetic powder is 10 parts by weight of magnetic powder per 100 parts by weight of resin.
The amount is 0 to 900 parts by weight, preferably 200 to 800 parts by weight. Below, the present invention will be explained in more detail based on production examples, working examples, and comparative examples.
製造例1
成分 重11部−
スチレン 60n−ブチルメタ
クリレート 35メタクリル酸・
5上記酸分をサンドスターラーにより充分に
混合して、重合性組成物を調製した。該組成物をアラビ
アゴム水溶液(濃度3重量%)中に加え、撹拌機(T、
にホモジナイザー、特殊工業(株)製)にて撹拌(30
00rpm)l、ながら60℃にて6時間重合反応を行
い、さらに80℃に昇温しで重合反応を行った。反応終
了後、反応系を冷却して5〜6回水洗し、濾過、乾燥し
て球形粒子を得た。得られた球形粒子の平均粒径は10
.2μl、軟化点(Tm)は141’C、ガラス転移点
(Ts)は61℃であった。
製造例2
シード重合法により得られた単分散球状のスチレン系ポ
リマー(平均粒径7μ肩、粒径の変動係数10%以内、
軟化点128℃、ガラス転移点54℃)をポリマー粒子
(A)とする。
該ポリマー粒子(A)100重量部とカーボンブラック
(三菱化成工業(株)MA#8)5重量部を101ヘン
シエルミキサーを用い1500 rpmにて5分間混合
撹拌し、カーボンブラックで表面が被覆されたポリマー
粒子(B)を得た。
次に、このポリマー粒子(B)100重量部と、ポリア
クリル酸ナトリウム5重量部を溶解した水2000重量
部とを混合撹拌し、中間粒子が水中に分散した系を得た
。ついで、この分散系にスチレン/n−ブチルメタアク
リレート/2,2,2.−トリフルオロエチルアクリレ
ート=75/15/10の組成比のモノマー100重量
部、重合開始剤として過硫酸カリウム2重量部を添加し
、系の温度を80℃に上昇させて6時間にわたり重合を
行い、ポリマー粒子(B)上にさらに樹脂コート層を有
するトナー粒子を得た。トナー粒子は平均粒径1081
1粒径の変動係数は11%であった。Production Example 1 Ingredients 11 parts by weight - Styrene 60 N-butyl methacrylate 35 Methacrylic acid.
5 The above acid components were sufficiently mixed using a sand stirrer to prepare a polymerizable composition. The composition was added to an aqueous gum arabic solution (concentration 3% by weight), and a stirrer (T,
Stir with a homogenizer (manufactured by Tokushu Kogyo Co., Ltd.) (30
The polymerization reaction was carried out at 60° C. for 6 hours at 00 rpm), and the temperature was further raised to 80° C. to carry out the polymerization reaction. After the reaction was completed, the reaction system was cooled, washed with water 5 to 6 times, filtered, and dried to obtain spherical particles. The average particle size of the obtained spherical particles was 10
.. 2 μl, the softening point (Tm) was 141'C, and the glass transition point (Ts) was 61°C. Production Example 2 Monodisperse spherical styrenic polymer obtained by seed polymerization method (average particle size of 7 μm, coefficient of variation of particle size within 10%,
Polymer particles (A) have a softening point of 128°C and a glass transition point of 54°C. 100 parts by weight of the polymer particles (A) and 5 parts by weight of carbon black (Mitsubishi Chemical Industries, Ltd. MA#8) were mixed and stirred at 1500 rpm for 5 minutes using a 101 Henschel mixer to coat the surface with carbon black. Polymer particles (B) were obtained. Next, 100 parts by weight of the polymer particles (B) and 2000 parts by weight of water in which 5 parts by weight of sodium polyacrylate were dissolved were mixed and stirred to obtain a system in which intermediate particles were dispersed in water. Then, styrene/n-butyl methacrylate/2,2,2. - 100 parts by weight of a monomer with a composition ratio of trifluoroethyl acrylate = 75/15/10 and 2 parts by weight of potassium persulfate as a polymerization initiator were added, the temperature of the system was raised to 80°C, and polymerization was carried out for 6 hours. , toner particles further having a resin coat layer on the polymer particles (B) were obtained. Toner particles have an average particle size of 1081
The coefficient of variation for one particle size was 11%.
【クリーニング用不定形トナーの製造】製造例3〔(+
)帯電性トナー〕
成 分 重量部スチレン
−n−ブチルメタ 100クリレート樹
脂
(軟化点=132℃、ガラス転移点二6転移点力−ボン
ブラック 5(三菱化成工
業(株)製、MA#8)
ニグロシン染料 3(オ
リエント化学(株)製、ボントロンN−01)上記材料
をボールミルで充分混合した後、140℃に加熱した3
本ロール上で混練した。混練物を放置冷却後、フェザ−
ミルを用い粗粉砕し、さらにジェットミルで微粉砕した
。つぎに、風力分級し、平均粒径8μmの微粉末を得た
。
製造例4 ((−)帯電性トナー〕
つぎの組成により製造例1と同様の方法を用いてトナー
を製造した。
酸価25.水酸価38)
カーボンブラック 5(三菱化
成工業(株)製、MA#8)[Production of amorphous toner for cleaning] Production example 3 [(+
) Chargeable toner] Ingredients Parts by weight Styrene-n-butyl meth 100 Acrylate resin (Softening point = 132°C, Glass transition point 26 Transition point power-Bon Black 5 (Mitsubishi Chemical Industries, Ltd., MA#8) Nigrosine Dye 3 (manufactured by Orient Chemical Co., Ltd., Bontron N-01) After thoroughly mixing the above materials in a ball mill, the dye 3 was heated to 140°C.
It was kneaded on the main roll. After cooling the kneaded material, feather
It was coarsely ground using a mill and further finely ground using a jet mill. Next, air classification was performed to obtain a fine powder with an average particle size of 8 μm. Production Example 4 ((-) Chargeable Toner) A toner was produced using the same method as Production Example 1 with the following composition. Acid value: 25. Hydroxy value: 38) Carbon black 5 (manufactured by Mitsubishi Chemical Industries, Ltd.) , MA#8)
製造例5
酸価23.水酸価40)
無機磁性粉 500(戸田工業
(株)製、EPT−1000)カーボンブラック
2(三菱化成工業(株)製、MA#8
)
上記材料をヘンシェルミキサーにより充分混合粉砕し、
次いで、シリンダ部180℃、シリンダヘッド部170
℃に設定した押出し混練機を用いて、溶融、混練した。
混練物を冷却後ジェットミルで微粉砕したのち、分級機
を用いて分級し、平均粒径55μmの磁性キャリアを得
た。
製造例6
ビスフェノール型ポリエステル樹脂(軟化点123℃;
ガラス転移点65℃;AV、21)のトルエン溶液(2
%溶液)を調整した。ついで芯材フェライトF−25Q
HR(平均粒径50μ禦;電気抵抗3.50X10’Ω
cl;日本鉄粉(株)製)30゜0重量部をスピラーコ
ータ5P−40(開田精工(株)製)を用いスプレー圧
3.5 kg/am、スプレー量40 g10+in、
温度50℃の条件にて120分処理した。得られた粒子
をフルイ(目開き: 105μl)を用い凝集物を除去
してコートキャリア(a)を得た。
前記コートキャリア(a)400重量部とFe−・Zn
系フェライト微粒子MFP−2(電気抵抗5.21XI
O@Ωam ; TDK(株)製)4重量部をオングミ
ルAM−20F(ホソカワミクロン(昧)製)を用い回
転数1100Orpにて40分間処理した。得られたキ
ャリア粒子をフルイ(フルイ目開き;105μR)によ
り凝集物を除去しキャリアを得た。
実施例1
製造例1で得られた球形トナー(+帯電性)と製造例5
で得られたキャリアとを用い、トナー混合比8wt%の
現像剤を得て主現像装置に装填した。
一方、前記キャリアとクリーニング用不定形粒子の製造
例3にて得られた不定形粒子(+帯電性)とをクリーニ
ング用現像装置に装填し第1図に示す電子写真複写装置
にて複写を行った。プロセス条件はつぎの通りである。
システム速度 28 cm/sec感光体表面電
位 −700■
現像バイアス −150V
イレース光量 10001ux
その結果優れた画像が得られ、またクリーニング不良は
まったくなかった。
実施例2
製造例2にて得られた球形トナー(+帯電性)を用いた
以外は前記実施例1と同様にして複写を行った。その結
果高品位の画像が得られ、またクリーニング不良は全く
認められなかった。
実施例3゜
製造例2で得られた球形トナー(+帯電性)と製造例6
で得られたキャリアとを用い、トナー混合比8wt%の
現像剤を得て主現像装置に装填した。
一方、前記キャリアとクリーニング用不定形粒子の製造
例3にて得られた不定形粒子(+帯電性)とをクリーニ
ング用現像装置に装填し第1図に示す電子写真複写装置
にて複写を行った。プロセス条件はつぎの通りである。
システム速度 20 cm/see感光体表面電
位 −550v
現像バイアス −100V
イレース光量 10001ux
その結果優れた画像が得られ、またクリーニング不良は
まったくなかった。
実施例4
システム速度を35 am/secとした以外は実施例
1と同様にして複写を行った。その結果優れた画像が得
られ、またクリーニング不良は全く認められなかった。
すなわち、本発明の方法によれば、システム速度に拘わ
らず優れたクリーニング性能を得ることができ、球形ト
ナーを使用してもクリーニング不良のない、安定し、た
高品位の画像を得ることができる。
実施例5〜8
前記実施例1〜4においてクリーニング用不定形トナー
を製造例4にて得られた不定形トナーとし、プロセス条
件においてクリーニング用現像バイアスの極性を逆とし
た以外は各々実施例1〜4と同様にして複写を行った。
いずれも優れた画像が得られ、またクリーニング不良は
全く認められなかった。
実施例9
クリーニング用不定形粒子として、製造例4にて用いた
スチレン−n−ブチルメタクリレート樹脂(軟化点13
2℃;ガラス転移点60℃)をジェット粉砕機により粉
砕し、平均粒径8μ友としたものを用いた以外は実施例
1と同様にして複写を行った。その結果優れた画像が得
られ、またクリーニング不良はなかった。
比較例1〜4
第1図においてクリーニング用現像装置17を取り除い
た以外は実施例1〜4とまったく同様にして作像を行っ
た。その結果いずれも第1枚目のコピー画像は優れてい
たものの第2枚目からはクリーニング不良発生のため、
コピー枚数とともに画質は低下していった。
このように不定形粒子を用いたクリーニング用現像装置
を装備しないで、球形トナーを用いると、クリーニング
不良が発生し安定して優れた画像を得ることができない
。
発明の効果
本発明方法によれば、高精細、緻密な画像が得られ、し
かも感光体のクリーニング性が優れる。Production example 5 Acid value 23. Hydroxyl value 40) Inorganic magnetic powder 500 (manufactured by Toda Kogyo Co., Ltd., EPT-1000) Carbon black
2 (manufactured by Mitsubishi Chemical Industries, Ltd., MA#8
) Thoroughly mix and grind the above materials using a Henschel mixer,
Next, the cylinder part is heated to 180°C, and the cylinder head part is heated to 170 degrees Celsius.
The mixture was melted and kneaded using an extrusion kneader set at ℃. After cooling, the kneaded material was finely pulverized using a jet mill, and then classified using a classifier to obtain a magnetic carrier having an average particle size of 55 μm. Production Example 6 Bisphenol type polyester resin (softening point 123°C;
Glass transition point: 65°C; AV, 21) in toluene solution (2
% solution) was adjusted. Next, core material ferrite F-25Q
HR (average particle size 50μ; electrical resistance 3.50X10'Ω
cl: 30°0 parts by weight (manufactured by Nippon Tetsuko Co., Ltd.) was sprayed using Spiller Coater 5P-40 (manufactured by Kaida Seiko Co., Ltd.) at a pressure of 3.5 kg/am and a spray amount of 40 g10+in.
The treatment was carried out for 120 minutes at a temperature of 50°C. A coated carrier (a) was obtained by removing aggregates from the obtained particles using a sieve (mesh size: 105 μl). 400 parts by weight of the coat carrier (a) and Fe-Zn
Ferrite fine particles MFP-2 (electrical resistance 5.21XI
4 parts by weight of O@Ωam (manufactured by TDK Corporation) was treated for 40 minutes at a rotational speed of 1100 Orp using Ongmill AM-20F (manufactured by Hosokawa Micron). Aggregates were removed from the obtained carrier particles using a sieve (sieve opening: 105 μR) to obtain a carrier. Example 1 Spherical toner (+ chargeability) obtained in Production Example 1 and Production Example 5
A developer having a toner mixing ratio of 8 wt % was obtained using the carrier obtained in step 1 and loaded into the main developing device. On the other hand, the carrier and the amorphous particles (+chargeable) obtained in Production Example 3 of Amorphous Particles for Cleaning were loaded into a developing device for cleaning, and copies were made using the electrophotographic copying device shown in FIG. Ta. The process conditions are as follows. System speed: 28 cm/sec Photoreceptor surface potential: -700 ■ Developing bias: -150 V Erase light amount: 10,001 ux As a result, an excellent image was obtained, and there were no cleaning defects at all. Example 2 Copying was carried out in the same manner as in Example 1 except that the spherical toner (+ chargeability) obtained in Production Example 2 was used. As a result, high-quality images were obtained, and no cleaning defects were observed. Example 3゜Spherical toner (+ chargeability) obtained in Production Example 2 and Production Example 6
A developer having a toner mixing ratio of 8 wt % was obtained using the carrier obtained in step 1 and loaded into the main developing device. On the other hand, the carrier and the amorphous particles (+chargeable) obtained in Production Example 3 of Amorphous Particles for Cleaning were loaded into a developing device for cleaning, and copies were made using the electrophotographic copying device shown in FIG. Ta. The process conditions are as follows. System speed 20 cm/see Photoreceptor surface potential -550v Developing bias -100V Erase light amount 10001ux As a result, excellent images were obtained and there were no cleaning defects. Example 4 Copying was carried out in the same manner as in Example 1 except that the system speed was 35 am/sec. As a result, excellent images were obtained, and no cleaning defects were observed. That is, according to the method of the present invention, excellent cleaning performance can be obtained regardless of the system speed, and stable, high-quality images without cleaning defects can be obtained even when using spherical toner. . Examples 5 to 8 In Examples 1 to 4, the amorphous toner obtained in Production Example 4 was used as the amorphous toner for cleaning, and the polarity of the developing bias for cleaning was reversed in the process conditions. Copying was carried out in the same manner as in 4. In all cases, excellent images were obtained, and no cleaning defects were observed. Example 9 The styrene-n-butyl methacrylate resin (softening point 13) used in Production Example 4 was used as amorphous particles for cleaning.
Copying was carried out in the same manner as in Example 1, except that a material (2° C.; glass transition point: 60° C.) was pulverized with a jet pulverizer to give an average particle size of 8 μm. As a result, excellent images were obtained, and there were no cleaning defects. Comparative Examples 1 to 4 Images were formed in exactly the same manner as Examples 1 to 4 except that the cleaning developing device 17 in FIG. 1 was removed. As a result, although the first copy image was excellent, poor cleaning occurred from the second copy.
The image quality deteriorated as the number of copies was increased. If a spherical toner is used without being equipped with a developing device for cleaning using amorphous particles as described above, poor cleaning will occur and a stable and excellent image cannot be obtained. Effects of the Invention According to the method of the present invention, high-definition, dense images can be obtained, and the cleaning properties of the photoreceptor are excellent.
第1図は本発明方法を実施する装置の概略断面図である
。
図中の主な符号はつぎの通りである。
1:現像装置、10:感光体ドラム、13:主現像装置
、17:クリーニング用現像装置、18:クリーニング
ブレード。
特許出願人 ミノルタカメラ株式会社FIG. 1 is a schematic sectional view of an apparatus for carrying out the method of the invention. The main symbols in the figure are as follows. 1: developing device, 10: photosensitive drum, 13: main developing device, 17: developing device for cleaning, 18: cleaning blade. Patent applicant Minolta Camera Co., Ltd.
Claims (1)
、転写後に感光体表面を不定形の粒子により現像操作を
行い、その後感光体のクリーニングを行うことを特徴と
する電子写真作像方法。(1) An electrophotographic developing method using spherical toner, which is characterized in that after transfer, the surface of the photoreceptor is developed with irregularly shaped particles, and then the photoreceptor is cleaned.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP28459487A JPH01126670A (en) | 1987-11-11 | 1987-11-11 | Electrophotographic image producing method |
US07/885,236 US5220390A (en) | 1987-11-11 | 1992-05-19 | Electrophotographic image forming process |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP28459487A JPH01126670A (en) | 1987-11-11 | 1987-11-11 | Electrophotographic image producing method |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01126670A true JPH01126670A (en) | 1989-05-18 |
Family
ID=17680477
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP28459487A Pending JPH01126670A (en) | 1987-11-11 | 1987-11-11 | Electrophotographic image producing method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01126670A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6517985B2 (en) | 2000-12-05 | 2003-02-11 | Fuji Xerox Co., Ltd. | Electrophotographic developer and process for forming image |
JP2007011298A (en) * | 2005-05-30 | 2007-01-18 | Kyocera Mita Corp | Image forming apparatus and image forming method |
JP2007187797A (en) * | 2006-01-12 | 2007-07-26 | Kyocera Mita Corp | Image forming apparatus |
-
1987
- 1987-11-11 JP JP28459487A patent/JPH01126670A/en active Pending
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6517985B2 (en) | 2000-12-05 | 2003-02-11 | Fuji Xerox Co., Ltd. | Electrophotographic developer and process for forming image |
JP2007011298A (en) * | 2005-05-30 | 2007-01-18 | Kyocera Mita Corp | Image forming apparatus and image forming method |
JP2007187797A (en) * | 2006-01-12 | 2007-07-26 | Kyocera Mita Corp | Image forming apparatus |
JP4490373B2 (en) * | 2006-01-12 | 2010-06-23 | 京セラミタ株式会社 | Image forming apparatus |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US5512406A (en) | Toners of different size for electrophotography | |
JP2612568B2 (en) | Electrophotographic toner | |
US5763229A (en) | Toner for developing electrostatic latent image | |
US6982139B2 (en) | Electrophotographic color toner, and electrophotographic color developer, toner cartridge, image forming device and image forming method using the same | |
JPH09127737A (en) | Electrostatic image developing carrier | |
JP3093578B2 (en) | Electrophotographic toner | |
JP2000039742A (en) | Magnetic coated carrier and two-component developer using same | |
US5220390A (en) | Electrophotographic image forming process | |
JPH01126670A (en) | Electrophotographic image producing method | |
JP4165822B2 (en) | Full color toner kit, process cartridge, image forming method and image forming apparatus | |
JPH06317933A (en) | Magnetic toner and electrophotographic method | |
JP3535082B2 (en) | Electrostatic image developing toner and image forming method | |
JP2003021930A (en) | Electrophotographic device and process cartridge | |
JPH06506782A (en) | Electrophotographic developer composition | |
JP4261642B2 (en) | Magnetic toner for development and development method | |
JPH0511497A (en) | Toner for developing electrostatic latent image | |
JP2007292854A (en) | Two-component developer and image forming method | |
JPS59102249A (en) | Developer used for electrostatic charge image | |
JPH07199520A (en) | Electrophotographic developer | |
JP2002055480A (en) | Electrophotographic toner and method for forming image | |
JPH06250546A (en) | Image forming method | |
JP2760048B2 (en) | Developer for printer | |
JPH04288554A (en) | Electrophotographic image forming method | |
JPS62168162A (en) | Electrophotographic method | |
JPS5891462A (en) | Positive charging magnetic toner for pressure fixing |