JPH1090995A - Developer carrier and developing device using the same - Google Patents
Developer carrier and developing device using the sameInfo
- Publication number
- JPH1090995A JPH1090995A JP5503197A JP5503197A JPH1090995A JP H1090995 A JPH1090995 A JP H1090995A JP 5503197 A JP5503197 A JP 5503197A JP 5503197 A JP5503197 A JP 5503197A JP H1090995 A JPH1090995 A JP H1090995A
- Authority
- JP
- Japan
- Prior art keywords
- developer
- particle diameter
- fine particles
- resin layer
- conductive fine
- 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
- 239000011347 resin Substances 0.000 claims abstract description 118
- 229920005989 resin Polymers 0.000 claims abstract description 118
- 239000002245 particle Substances 0.000 claims abstract description 81
- 239000010419 fine particle Substances 0.000 claims abstract description 61
- 230000001105 regulatory effect Effects 0.000 claims abstract description 8
- 230000002093 peripheral effect Effects 0.000 claims abstract description 7
- 230000005684 electric field Effects 0.000 claims abstract description 5
- 239000011230 binding agent Substances 0.000 claims description 25
- 239000005011 phenolic resin Substances 0.000 claims description 15
- 239000000758 substrate Substances 0.000 claims description 13
- 238000004132 cross linking Methods 0.000 claims description 11
- 239000011163 secondary particle Substances 0.000 claims description 6
- 239000006185 dispersion Substances 0.000 claims description 2
- 239000010410 layer Substances 0.000 description 86
- 230000000052 comparative effect Effects 0.000 description 17
- 238000000576 coating method Methods 0.000 description 11
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 10
- 239000011248 coating agent Substances 0.000 description 10
- 238000000034 method Methods 0.000 description 9
- 239000007921 spray Substances 0.000 description 9
- 230000003746 surface roughness Effects 0.000 description 9
- 239000006229 carbon black Substances 0.000 description 6
- 230000007423 decrease Effects 0.000 description 6
- 238000011161 development Methods 0.000 description 6
- 239000003085 diluting agent Substances 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 239000011324 bead Substances 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- 229910002804 graphite Inorganic materials 0.000 description 5
- 239000010439 graphite Substances 0.000 description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 230000009467 reduction Effects 0.000 description 4
- 230000008719 thickening Effects 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 238000007788 roughening Methods 0.000 description 3
- 239000004576 sand Substances 0.000 description 3
- 239000010935 stainless steel Substances 0.000 description 3
- 229910001220 stainless steel Inorganic materials 0.000 description 3
- 238000012546 transfer Methods 0.000 description 3
- 230000032258 transport Effects 0.000 description 3
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 241001422033 Thestylus Species 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- HNAGHMKIPMKKBB-UHFFFAOYSA-N 1-benzylpyrrolidine-3-carboxamide Chemical compound C1C(C(=O)N)CCN1CC1=CC=CC=C1 HNAGHMKIPMKKBB-UHFFFAOYSA-N 0.000 description 1
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-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
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 238000012935 Averaging Methods 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004695 Polyether sulfone Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 229920006311 Urethane elastomer Polymers 0.000 description 1
- 235000010724 Wisteria floribunda Nutrition 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 229910000410 antimony oxide Inorganic materials 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- OBNCKNCVKJNDBV-UHFFFAOYSA-N butanoic acid ethyl ester Natural products CCCC(=O)OCC OBNCKNCVKJNDBV-UHFFFAOYSA-N 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 239000003575 carbonaceous material Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910003437 indium oxide Inorganic materials 0.000 description 1
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 108091008695 photoreceptors Proteins 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920006393 polyether sulfone Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920006380 polyphenylene oxide Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000011164 primary particle Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 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
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Dry Development In Electrophotography (AREA)
- Rolls And Other Rotary Bodies (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、電子写真複写機、
レーザプリンター、ファクシミリ等の電子写真方式を採
用した画像形成装置における現像装置に関する。詳しく
は、現像剤層厚規制部材によって樹脂層表面への付着量
が規制される現像剤を現像領域に搬送する現像剤担持
体、および静電潜像保持体と現像剤担持体の間の電界に
よって静電潜像保持体表面に形成された静電潜像を現像
する現像装置に関する。The present invention relates to an electrophotographic copying machine,
The present invention relates to a developing device in an image forming apparatus employing an electrophotographic method such as a laser printer and a facsimile. More specifically, a developer carrier that conveys a developer whose amount of adhesion to the resin layer surface is regulated by the developer layer thickness regulating member to a development area, and an electric field between the electrostatic latent image carrier and the developer carrier The present invention relates to a developing device for developing an electrostatic latent image formed on the surface of an electrostatic latent image holding member.
【0002】[0002]
【従来の技術】電子写真方式を採用した画像形成装置に
おいて、静電潜像保持体(感光体)に形成された静電潜
像を現像する方法として、使用する現像剤の種類等に応
じて各種の方法が従来から知られている。それらのう
ち、現像剤担持体表面に粗面化処理を施すことによって
現像剤の搬送性を向上させた現像装置が、例えば特開昭
55−140858公報、同56−1131728公
報、同57−66455公報等に記載されている。一成
分現像剤を使用する現像装置では、現像剤は現像剤担持
体との摩擦帯電により静電潜像を現像するに必要な極性
の電荷が与えられる。上記粗面化処理された現像剤担持
体は、現像剤を適切に摩擦帯電させることにも寄与して
いる。また、一成分現像装置では、摩擦帯電性制御、搬
送性制御の改善および画像欠陥防止のために、表面に導
電性微粒子が分散した樹脂層を形成した現像剤担持体が
用いられている。これらの現像剤担持体では、その表面
粗さは算術平均粗さRa等の指標で規定されている。例
えば、特開平4−6089号公報には、粗面化処理され
た基体を導電性の樹脂でコーティングした後の表面粗さ
を算術平均粗さRaで0.8〜2.5μmの範囲に規定し
ている。2. Description of the Related Art In an image forming apparatus employing an electrophotographic system, a method of developing an electrostatic latent image formed on an electrostatic latent image holding member (photoreceptor) depends on the type of developer used and the like. Various methods are conventionally known. Among them, a developing device in which the developer carrying property is improved by subjecting the surface of the developer carrying member to a roughening process is disclosed in, for example, JP-A-55-140858, JP-A-56-11131728, and JP-A-57-66455. It is described in gazettes and the like. In a developing device using a one-component developer, a charge of a polarity necessary for developing an electrostatic latent image is given to the developer by frictional charging with a developer carrier. The developer carrier having been subjected to the surface roughening also contributes to appropriate frictional charging of the developer. Further, in the one-component developing apparatus, a developer carrier having a resin layer in which conductive fine particles are dispersed is used on the surface to improve the control of frictional charging property and the control of transportability and to prevent image defects. In these developer carrying members, the surface roughness is defined by an index such as an arithmetic average roughness Ra. For example, Japanese Patent Application Laid-Open No. 4-6089 discloses that the surface roughness after coating a substrate subjected to a surface roughening treatment with a conductive resin is defined as an arithmetic average roughness Ra in a range of 0.8 to 2.5 μm. doing.
【0003】しかしながら、表面に樹脂層を形成した現
像剤担持体を用いた従来の一成分現像装置では、現像剤
が現像剤担持体表面に接着しやすいことから、画像濃度
低下の原因である現像剤固着(トナーフィルミング)を
発生することがある。また、樹脂層を形成した現像剤担
持体は粒子径がトナー粒子径以下の数nm〜数μmの導
電性微粒子が樹脂層に添加されており、これらの導電性
微粒子が現像剤担持体表面に突起を形成し、現像剤の機
械的な固着の原因となってしまう。このように、現像剤
担持体への現像剤の固着は、現像剤と現像剤担持体との
接着性や現像剤担持体から現像剤への熱エネルギーの移
動、あるいは現像剤が現像剤担持体に機械的に削られて
しまうことに起因して生じるものである。つまり、現像
剤担持体表面におけるトナー粒子径よりも微小な大きさ
の凹凸が関与しているのである。算術平均粗さRa等
は、トナー粒子径以上の凹凸を表す指標としては優れて
いるが、上述の微小な凹凸に対しては、従来のような表
面粗さの測定および指標では測定装置の横方向の感度の
低さから、凹凸を表す指標とはなり得ない。したがっ
て、従来の表面粗さの規定だけでは、現像剤担持体への
現像剤の固着を回避することが困難である。However, in a conventional one-component developing apparatus using a developer carrying member having a resin layer formed on the surface, the developer tends to adhere to the surface of the developer carrying member, and thus, the development which causes a decrease in image density is difficult. Agent sticking (toner filming) may occur. Further, in the developer carrier having the resin layer formed thereon, conductive fine particles having a particle diameter of several nm to several μm or less of the toner particle diameter are added to the resin layer, and these conductive fine particles are deposited on the surface of the developer carrier. Protrusions are formed, which causes mechanical fixation of the developer. As described above, the adhesion of the developer to the developer carrier is caused by the adhesion between the developer and the developer carrier, the transfer of thermal energy from the developer carrier to the developer, or the transfer of the developer by the developer carrier. This is caused by mechanical shaving. That is, irregularities smaller than the toner particle diameter on the surface of the developer carrying member are involved. Arithmetic average roughness Ra and the like are excellent as indices representing irregularities equal to or larger than the toner particle diameter. Due to the low sensitivity in the direction, it cannot be used as an index indicating the unevenness. Therefore, it is difficult to avoid the fixation of the developer to the developer carrier only by the conventional regulation of the surface roughness.
【0004】[0004]
【発明が解決しようとする課題】このように、表面に樹
脂層を被覆した従来の現像剤担持体では、現像剤の固着
を回避することは困難であるという問題があった。そこ
で、本発明は、上述の問題点を解決しようとするもので
あって、適正な画像濃度および高画質を維持しつつ、現
像剤担持体への現像剤の固着を回避することが可能な現
像剤担持体および同現像剤担持体を用いた現像装置を提
供することにある。As described above, there is a problem that it is difficult to avoid sticking of the developer in the conventional developer bearing member having the surface coated with the resin layer. Accordingly, the present invention is directed to solving the above-described problems, and a developing method capable of avoiding sticking of a developer to a developer carrying member while maintaining proper image density and high image quality. An object of the present invention is to provide a developer carrier and a developing device using the developer carrier.
【0005】[0005]
【課題を解決するための手段】本発明者は、導電性樹脂
層を表面層とする現像剤担持体を備えた現像装置におい
て、現像剤担持体への現像剤の固着の問題を解消すべく
鋭意研究・検討を重ねてきたところ、従来の算術平均粗
さRaの他に新たに有効線長さSRlrを表面粗さの指
標として導入すると共に、この有効線長さを従来の値よ
り小さくすることによって、上記目的が達成されること
を見い出し、本発明をなすに到ったものである。すなわ
ち、本発明の現像剤担持体は、導電性微粒子を含有する
結着樹脂からなる樹脂層が円筒状基体の外周面に被覆さ
れ、樹脂層表面にはトナー粒子径より大きい凹凸とトナ
ー粒子径より小さい凹凸が形成され、トナー粒子径より
大きい凹凸が算術平均粗さRaで1.3〜1.8μmの範
囲にあり、かつトナー粒子径より小さい凹凸が有効線長
さSRlrで104%以下であることを特徴とする。ま
た、本発明の現像装置は、上記現像剤担持体を用いるこ
とを特徴とする。SUMMARY OF THE INVENTION The present inventor has sought to solve the problem of sticking of a developer to a developer carrier in a developing device having a developer carrier having a conductive resin layer as a surface layer. After extensive studies and studies, the effective line length SRlr is newly introduced as an index of the surface roughness in addition to the conventional arithmetic average roughness Ra, and the effective line length is made smaller than the conventional value. As a result, it has been found that the above-mentioned object is achieved, and the present invention has been accomplished. That is, in the developer carrier of the present invention, a resin layer composed of a binder resin containing conductive fine particles is coated on the outer peripheral surface of the cylindrical substrate, and the resin layer surface has irregularities larger than the toner particle diameter and the toner particle diameter. Smaller irregularities are formed, irregularities larger than the toner particle diameter are in the range of 1.3 to 1.8 μm in arithmetic average roughness Ra, and irregularities smaller than the toner particle diameter are 104% or less in effective line length SRlr. There is a feature. Further, a developing device of the present invention is characterized by using the above-mentioned developer carrier.
【0006】[0006]
【発明の実施の形態】以下、本発明を詳細に説明する。
本発明の現像剤担持体は、円筒状基体の外周面に現像剤
を担持する樹脂層が被覆されている。樹脂層は結着樹脂
に少なくとも導電性微粒子を含有した導電性層からな
り、結着樹脂中には導電性微粒子が分散している。円筒
状基体としては、例えばアルミニウム,ステンレス鋼等
の非磁性で導電性の部材が用いられる。上記樹脂層を構
成する結着樹脂としては、フェノール樹脂,メラミン樹
脂,尿素樹脂,アルキド樹脂,エポキシ樹脂,ポリアミ
ド,ポリイミド,ポリエステル,ポリウレタン,ポリカ
ーボネート,ポリフェニレンオキサイド,ポリエーテル
スルホン,アクリル系樹脂,スチレン系樹脂や、離型性
に優れているフッ素系樹脂,シリコーン樹脂等が好まし
く用いられる。BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be described in detail.
In the developer carrier of the present invention, a resin layer for carrying the developer is coated on the outer peripheral surface of the cylindrical substrate. The resin layer is formed of a conductive layer containing at least conductive fine particles in a binder resin, and the conductive fine particles are dispersed in the binder resin. As the cylindrical substrate, a non-magnetic conductive member such as aluminum or stainless steel is used. Examples of the binder resin constituting the resin layer include phenol resin, melamine resin, urea resin, alkyd resin, epoxy resin, polyamide, polyimide, polyester, polyurethane, polycarbonate, polyphenylene oxide, polyether sulfone, acrylic resin, and styrene resin. Resins, fluorine-based resins, silicone resins, and the like, which are excellent in releasability, are preferably used.
【0007】樹脂層に分散する導電性微粒子としては、
カーボンブラック,これを造粒したカーボンビーズ,カ
ーボンファイバー,グラファイト等の炭素系物質、銅,
銀,アルミニウム,ステンレス鋼等の導電性金属または
合金、酸化錫,酸化インジウム,酸化アンチモン,酸化
チタン,Sn2O−In2O3 複合酸化物等の導電性金属
酸化物、チタン酸カリウム等の導電性ウィスカーなどの
微粉末が用いられる。本発明においては、樹脂層中にト
ナー粒子径より大きい導電性微粒子を分散させて、樹脂
層表面にトナー粒子径より大きい凹凸を形成し、現像剤
の搬送性の制御を行う。その際、樹脂層表面には、導電
性微粒子の表面形状やその表面分布等に応じて、トナー
粒子径より小さい凹凸も同時に形成される。また、樹脂
層中にトナー粒子径より大きいものと小さいもののサイ
ズの異なる導電性微粒子を分散させることが好ましい。
その場合は、現像剤担持体の抵抗を適正値に制御するこ
とが容易となり、現像剤に適正な帯電量を付与すること
ができる。なお、トナー粒子径とはその体積平均粒子径
を意味し、通常4〜13μmの範囲にあるトナーが使用
される。The conductive fine particles dispersed in the resin layer include:
Carbon black, carbon beads obtained by granulating the carbon black, carbon fibers, carbon-based substances such as graphite, copper,
Conductive metals or alloys such as silver, aluminum and stainless steel, conductive metal oxides such as tin oxide, indium oxide, antimony oxide, titanium oxide, Sn 2 O—In 2 O 3 composite oxide, potassium titanate, etc. Fine powder such as a conductive whisker is used. In the present invention, conductive fine particles larger than the toner particle diameter are dispersed in the resin layer to form irregularities larger than the toner particle diameter on the surface of the resin layer, thereby controlling the developer transportability. At this time, irregularities smaller than the toner particle diameter are simultaneously formed on the surface of the resin layer according to the surface shape and the surface distribution of the conductive fine particles. Further, it is preferable to disperse conductive fine particles having a size larger than and smaller than the toner particle size in the resin layer.
In that case, it becomes easy to control the resistance of the developer carrier to an appropriate value, and an appropriate charge amount can be given to the developer. In addition, the toner particle diameter means its volume average particle diameter, and a toner in the range of 4 to 13 μm is usually used.
【0008】前者の導電性微粒子の一次平均粒子径は、
使用されるトナー粒子径より大きくかつ15μm以下が
好適である。一例として、体積平均粒子径7μmの現像
剤を使用した場合、平均粒子径10μmの導電性微粒子
が用いられる。その具体的な微粒子としては、樹脂層に
潤滑性を付与する作用のあるグラファイトや、カーボン
ビーズ等が好ましく用いられる。また、後者の導電性微
粒子の一次平均粒子径は、トナー粒子径より小さく、か
つ10nm(二次平均粒子径で大凡数百nm程度)以上
が好適である。その具体的な微粒子としては、特に限定
されるものではないが、現像剤の過剰帯電を防止する作
用のあるカーボンブラックが好ましく用いられる。導電
性微粒子の好ましい使用量(含有量)は、微粒子の種類
によっても異なるが、結着樹脂100重量部に対して、
前者のサイズの大きい導電性微粒子が30〜60重量部
の範囲であり、また後者のサイズの小さい導電性微粒子
が30重量部以下までの範囲で前者と併用することがで
きる。The primary average particle diameter of the former conductive fine particles is
It is preferable that the diameter is larger than the used toner particle diameter and 15 μm or less. As an example, when a developer having a volume average particle diameter of 7 μm is used, conductive fine particles having an average particle diameter of 10 μm are used. As the specific fine particles, graphite, carbon beads, and the like having an effect of imparting lubricity to the resin layer are preferably used. It is preferable that the latter conductive fine particles have a primary average particle diameter smaller than the toner particle diameter and 10 nm or more (approximately several hundred nm in secondary average particle diameter) or more. Specific examples of the fine particles include, but are not particularly limited to, carbon black having an action of preventing excessive charging of the developer. The preferred use amount (content) of the conductive fine particles varies depending on the type of the fine particles.
The former can be used together with the larger conductive fine particles in the range of 30 to 60 parts by weight, and the latter smaller conductive fine particles can be used in the range of up to 30 parts by weight or less.
【0009】導電性微粒子が分散した現像剤担持体表面
の凹凸については、算術平均粗さRaが1.3〜1.8μ
mの範囲になければならない。この平均粗さRaは、触
針式表面粗さ測定機(surfcom :東京精密社製)を使用
して樹脂層表面の凹凸を測定し、測定された十点での値
を平均したものである。ここで、平均粗さRaが1.3
μm未満の場合は、樹脂層表面が平滑になりすぎて現像
剤の搬送量が減少するため、適正な画像濃度を維持する
ことが困難となる。一方、平均粗さRaが1.8μmを
越える場合は、現像剤の搬送量が増加するため、画像上
の現像剤層が厚くなり、細線の太り等の画質劣化の原因
となる。更に、現像量が過多になるため、現像剤の使用
量が多くなりランニングコストにも影響する。Regarding the unevenness of the surface of the developer carrying member in which the conductive fine particles are dispersed, the arithmetic average roughness Ra is 1.3 to 1.8 μm.
m. The average roughness Ra is obtained by measuring the unevenness of the resin layer surface using a stylus type surface roughness measuring device (surfcom: manufactured by Tokyo Seimitsu Co., Ltd.) and averaging the measured values at ten points. . Here, the average roughness Ra is 1.3.
If it is less than μm, the surface of the resin layer becomes too smooth and the amount of developer transported decreases, making it difficult to maintain an appropriate image density. On the other hand, when the average roughness Ra exceeds 1.8 μm, the transport amount of the developer increases, so that the developer layer on the image becomes thick, which causes deterioration of image quality such as thickening of fine lines. Further, since the amount of development becomes excessive, the amount of developer used increases, which affects running costs.
【0010】本発明では、トナー粒子径よりも小さい凹
凸を表す指標として有効線長さSRlrを採用した。これ
は、樹脂層表面の断面形状の各周波数成分からトナー粒
子径以上の周波数成分をカットオフし、得られた粗さ曲
線の全長(a)を測定区間長(b)で割って百分率で表示し
たものである。図1は、樹脂層表面の上記カットオフ後
の粗さ曲線を示し、現像剤担持体の周方向に対して半径
方向の長さを強調して図示している。そして、有効線長
さSRlrは次のように定義される。 SRlr(%) = (a/b)×100 現像剤担持体表面への現像剤の固着を回避するために
は、トナー粒子径より小さい凹凸を減少させる必要があ
り、樹脂層表面に形成された凹凸の有効線長さSRlrが1
04%以下でなければならない。現像剤担持体の樹脂層
をコーティング法で形成する場合は、結着樹脂の種類と
その分子量,導電性微粒子の粒子径とその配合量や分散
性,塗布条件等により、有効線長さSRlrを調整すること
ができる。有効線長さSRlrを求めるには、現像剤担持体
表面の非常に微小な凹凸を測定する必要がある。そのた
め、本発明では、前記触針式表面粗さ測定機に代えて、
三次元表面形状解析装置(RD500:電子工学研究所
製)を使用する。この解析装置は、走査型電子顕微鏡
(S4200:日立製作所製)の反射電子信号から試料
表面の形状を解析する装置である。In the present invention, the effective line length SRlr is employed as an index representing the unevenness smaller than the toner particle diameter. This means that the frequency component of the toner particle diameter or more is cut off from each frequency component of the cross-sectional shape of the resin layer surface, and the total length (a) of the obtained roughness curve is divided by the measurement section length (b) and displayed as a percentage. It was done. FIG. 1 shows a roughness curve of the surface of the resin layer after the cutoff, in which the length in the radial direction with respect to the circumferential direction of the developer carrier is emphasized. Then, the effective line length SRlr is defined as follows. SRlr (%) = (a / b) × 100 In order to avoid sticking of the developer to the surface of the developer carrying member, it is necessary to reduce irregularities smaller than the toner particle diameter. Effective line length SRlr of unevenness is 1
Must be less than 04%. When the resin layer of the developer carrier is formed by a coating method, the effective line length SRlr is determined depending on the type and the molecular weight of the binder resin, the particle diameter of the conductive fine particles, the compounding amount, dispersibility, application conditions, and the like. Can be adjusted. In order to determine the effective line length SRlr, it is necessary to measure very minute irregularities on the surface of the developer carrying member. Therefore, in the present invention, instead of the stylus type surface roughness measuring device,
A three-dimensional surface shape analyzer (RD500: manufactured by Electronic Engineering Laboratory) is used. This analyzer analyzes the shape of the sample surface from reflected electron signals of a scanning electron microscope (S4200: manufactured by Hitachi, Ltd.).
【0011】前記結着樹脂としては、樹脂層の表面特
性,機械的強度,価格等の面でフェノール樹脂が特に好
適に用いられる。フェノール樹脂は、架橋前の重量平均
分子量Mwが4500以上であるものが好ましい。すな
わち、上記分子量Mwが4500未満であると、トナー
粒子径より小さい導電性微粒子の分散性が悪くなる。分
散性が悪化すると、これらの導電性微粒子の二次凝集体
の粒子径が大きくなり、コーティング後の現像剤担持体
表面にこれら二次凝集体が露出し、トナー粒子径より小
さい凹凸が増加して有効線長さSRlrが104%を越えて
しまう。その結果、現像剤担持体から現像剤への熱エネ
ルギーの移動が促進され、また現像剤が現像剤担持体に
機械的に削られてしまうため、現像剤担持体に現像剤の
固着が生じる。As the binder resin, a phenol resin is particularly preferably used in terms of the surface properties of the resin layer, mechanical strength, cost and the like. The phenol resin preferably has a weight average molecular weight Mw of 4500 or more before crosslinking. That is, when the molecular weight Mw is less than 4500, the dispersibility of the conductive fine particles smaller than the toner particle diameter becomes poor. When the dispersibility is deteriorated, the particle diameter of the secondary aggregate of these conductive fine particles increases, and these secondary aggregates are exposed on the surface of the developer carrier after coating, and irregularities smaller than the toner particle diameter increase. As a result, the effective line length SRlr exceeds 104%. As a result, the transfer of thermal energy from the developer carrier to the developer is promoted, and the developer is mechanically shaved by the developer carrier, so that the developer is fixed to the developer carrier.
【0012】前記樹脂層は次のようにして形成すること
ができる。まず、結着樹脂,導電性微粒子,希釈剤(溶
剤)、および必要に応じて各種添加剤等を混合し、更に
サンドミル等で固形分を均一に分散して塗布液を調製す
る。この際、希釈剤の混合割合を調節して塗布液の粘
度,造膜性を調節する。次いで、円筒状基体を回転させ
ながらその表面に塗布液を噴霧するエアスプレー法等に
よりコーティングし、130〜250℃で結着樹脂を硬
化させる。希釈剤としては、ヘキサン,ベンゼン,トル
エン,キシレン等の炭化水素類、メチルエチルケトン,
シクロヘキサノン等のケトン類、エタノール,イソプロ
パノール,ブタノール等のアルコール類、ジブチルエー
テル,テトラヒドロフラン,プロピレングリコールモノ
メチルエーテル等のエーテル類、酢酸エチル,酢酸ブチ
ル,酪酸エチル等のエステル類などが挙げられる。これ
らの希釈剤や前記結着樹脂および導電性微粒子は、単独
でもあるいは異なる物質を2種以上混合して用いてもよ
い。このようにして形成された樹脂層中には導電性微粒
子が分散した状態にあり、樹脂層表面から少なくとも導
電性微粒子の一部が突出して、前述したように、トナー
粒子径より大きい凹凸と小さい微細な凹凸とが共存した
状態にある。The resin layer can be formed as follows. First, a coating liquid is prepared by mixing a binder resin, conductive fine particles, a diluent (solvent), and various additives as necessary, and further uniformly dispersing a solid content with a sand mill or the like. At this time, the viscosity and the film forming property of the coating solution are adjusted by adjusting the mixing ratio of the diluent. Next, the surface of the cylindrical substrate is coated by an air spray method or the like while spraying a coating solution while rotating, and the binder resin is cured at 130 to 250 ° C. Diluents include hydrocarbons such as hexane, benzene, toluene and xylene, methyl ethyl ketone,
Examples include ketones such as cyclohexanone, alcohols such as ethanol, isopropanol and butanol, ethers such as dibutyl ether, tetrahydrofuran and propylene glycol monomethyl ether, and esters such as ethyl acetate, butyl acetate and ethyl butyrate. These diluents, the binder resin and the conductive fine particles may be used alone or as a mixture of two or more different substances. In the resin layer thus formed, the conductive fine particles are in a dispersed state, and at least a part of the conductive fine particles protrudes from the surface of the resin layer, and as described above, irregularities larger than the toner particle diameter are small. Fine irregularities coexist.
【0013】ところで、結着樹脂に対する導電性微粒子
の含有量が多くなると体積比率も高くなり、一般に導電
性微粒子が樹脂層表面に露出する割合が高くなる。同時
に、トナー粒子径より小さい導電性微粒子の個々の体積
が大きくなると、これらの微粒子が樹脂層表面に露出す
る割合も高くなる。このトナー粒子径より小さい導電性
微粒子は樹脂中に分散させても再凝集して二次粒子を形
成するため、樹脂層表面に形成される凹凸の程度は二次
粒子径に依存する。この二次粒子径は分散方法や結着樹
脂の架橋前の重量平均分子量によっても変化する。前記
有効線長さSRlrは専らトナー粒子径より小さい導電性微
粒子の樹脂層表面への露出具合によって定まるが、導電
性微粒子の粒子径および結着樹脂中の含有量が下記の式
で表される関係を満たしている場合、有効線長さSRlrを
104%以下に抑えることができる。すなわち、結着樹
脂に対するトナー粒子径より大きい導電性微粒子および
小さい導電性微粒子の含有量と粒子径を調整することに
よって、現像剤担持体表面への現像剤の固着を防止する
ことが可能である。 4.5×103×(R1)3V1 + (R2)3V2 < 300 ここで、R1 は樹脂層中のトナー粒子径より小さい導電
性微粒子の二次粒子径(μm)、V1 は結着樹脂1g当た
りのトナー粒子径より小さい導電性微粒子の含有量(g)
であり、R2 は塗布液中に分散した後のトナー粒子径よ
り大きい導電性微粒子の粒子径(μm)、V2 は結着樹脂
1g当たりのトナー粒子径より大きい導電性微粒子の含
有量(g)である。By the way, as the content of the conductive fine particles with respect to the binder resin increases, the volume ratio also increases, and in general, the ratio of the conductive fine particles exposed on the surface of the resin layer increases. At the same time, as the volume of each of the conductive fine particles smaller than the toner particle diameter increases, the rate of exposing these fine particles to the resin layer surface also increases. Even if the conductive fine particles smaller than the toner particle diameter are dispersed in the resin, they reaggregate to form secondary particles, and thus the degree of unevenness formed on the surface of the resin layer depends on the secondary particle diameter. This secondary particle diameter also changes depending on the dispersion method and the weight average molecular weight of the binder resin before crosslinking. The effective line length SRlr is determined solely by the degree of exposure of the conductive fine particles smaller than the toner particle diameter to the resin layer surface, and the particle diameter of the conductive fine particles and the content in the binder resin are represented by the following formula. When the relationship is satisfied, the effective line length SRlr can be suppressed to 104% or less. That is, it is possible to prevent the developer from sticking to the surface of the developer carrier by adjusting the content and the particle size of the conductive fine particles larger and smaller than the toner particle size with respect to the binder resin. . 4.5 × 10 3 × (R 1 ) 3 V 1 + (R 2 ) 3 V 2 <300 where R 1 is the secondary particle diameter (μm) of the conductive fine particles smaller than the toner particle diameter in the resin layer. , V 1 is the content (g) of the conductive fine particles smaller than the toner particle diameter per 1 g of the binder resin.
R 2 is the particle diameter (μm) of the conductive fine particles larger than the toner particle diameter after being dispersed in the coating solution, and V 2 is the content of the conductive fine particles larger than the toner particle diameter per 1 g of the binder resin ( g).
【0014】本発明の現像装置において使用される現像
剤は、現像剤担持体との摩擦接触により適切な帯電量が
得られるため、磁性一成分現像剤または非磁性一成分現
像剤であることが好ましい。しかし、キャリアを用いる
二成分現像剤も使用することが可能である。現像剤に
は、その流動性や帯電性を向上させる目的で、シリカ,
チタニア等の外添剤を添加することができる。外添剤の
一次粒子径は5〜50nmの範囲にあることが好まし
い。The developer used in the developing device of the present invention can be a magnetic one-component developer or a non-magnetic one-component developer because an appropriate charge amount can be obtained by frictional contact with a developer carrier. preferable. However, it is also possible to use a two-component developer using a carrier. In order to improve the fluidity and chargeability of the developer, silica,
An external additive such as titania can be added. The primary particle diameter of the external additive is preferably in the range of 5 to 50 nm.
【0015】本発明の作用は次のとおりである。なお、
本発明の要素には、理解を容易にするために、図2に示
す現像装置の要素と対応する符号を括弧内に付記する。
請求項1発明の現像剤担持体(4)は、樹脂層(4b)表面
におけるトナー粒子径より大きい凹凸が算術平均粗さR
aで1.3〜1.8μmの範囲にあるため、適正な現像剤
の搬送量および画像濃度を維持することができ、画像濃
度の低下や細線の太り等の画質劣化が生じるようなこと
はない。また、微細な表面粗さの指標として有効線長さ
SRlrを導入することにより、樹脂層(4b)表面における
トナー粒子径より小さい凹凸を有効線長さSRlrで104
%以下としたものである。その結果、現像剤(6)の固着
を回避することが可能となり、画像濃度の低下を防止す
ることができる。請求項2発明の現像剤担持体(4)は、
トナー粒子径より大きい導電性微粒子を樹脂層(4b)に
分散させたものである。したがって、適切な粒子径範囲
にある導電性微粒子を用いることにより、算術平均粗さ
Raを上記範囲に容易に調整することができる。The operation of the present invention is as follows. In addition,
For easy understanding, the components of the present invention are denoted by the same reference numerals in parentheses as those corresponding to the components of the developing device shown in FIG.
In the developer carrier (4) according to the first aspect of the present invention, irregularities larger than the toner particle diameter on the surface of the resin layer (4b) have an arithmetic average roughness R.
Since a is in the range of 1.3 to 1.8 μm, it is possible to maintain a proper amount of developer transport and image density, and it is possible to prevent image quality deterioration such as reduction in image density and thickening of thin lines. Absent. Also, effective line length is used as an index of fine surface roughness.
By introducing SRlr, irregularities smaller than the toner particle diameter on the surface of the resin layer (4b) are reduced by an effective line length SRlr of 104.
% Or less. As a result, the developer (6) can be prevented from sticking, and a decrease in image density can be prevented. The developer carrier (4) according to the second aspect of the present invention
The conductive fine particles larger than the toner particle diameter are dispersed in the resin layer (4b). Therefore, the arithmetic average roughness Ra can be easily adjusted to the above range by using the conductive fine particles having an appropriate particle diameter range.
【0016】請求項3発明の現像剤担持体(4)は、トナ
ー粒子径より大きい導電性微粒子と共にトナー粒子径よ
り小さい導電性微粒子を樹脂層(4b)に分散させたもの
である。したがって、適切な粒子径範囲にある大小2種
類の導電性微粒子を用いることにより、現像剤(6)に適
正な帯電量を付与することができる。請求項4発明の現
像剤担持体(4)は、導電性微粒子の粒子径および結着樹
脂中の含有量が次の関係式を満足するものである。な
お、式中のR1 ,V1 ,R2 ,V2 は前述の粒子径また
は含有量を意味する。 4.5×103×(R1)3V1 + (R2)3V2 < 300 上記粒子径および含有量相互の関係が上記式を満足する
場合、前記有効線長さSRlrは104%以下となるので、
現像剤が担持体表面に固着することがない。請求項5発
明の現像剤担持体(4)は、樹脂層(4b)を構成する結着
樹脂としてフェノール樹脂を用い、その架橋前の重量平
均分子量Mwを4500以上としたものである。この発
明によれば、前記有効線長さSRlrが104%以下に調整
された樹脂層(4b)が容易に得られるため、現像剤担持
体(4)表面への現像剤(6)の固着による画像濃度の低下
を防止することができる。請求項6発明の現像装置(3)
は、請求項1発明〜請求項5発明のいずれかの現像剤担
持体(4)を用いるものである。したがって、上述の各請
求項発明と同様の作用を奏する。The developer carrier (4) of the present invention is obtained by dispersing conductive fine particles smaller than the toner particle size together with conductive fine particles larger than the toner particle size in the resin layer (4b). Therefore, by using two types of large and small conductive fine particles having an appropriate particle diameter range, the developer (6) can be given an appropriate charge amount. According to a fourth aspect of the present invention, the particle diameter of the conductive fine particles and the content in the binder resin satisfy the following relational expression. In the formula, R 1 , V 1 , R 2 , and V 2 mean the above-mentioned particle diameters or contents. 4.5 × 10 3 × (R 1 ) 3 V 1 + (R 2 ) 3 V 2 <300 When the relationship between the particle size and the content satisfies the above formula, the effective line length SRlr is 104%. Since
The developer does not adhere to the surface of the carrier. According to a fifth aspect of the present invention, the developer carrier (4) uses a phenol resin as a binder resin constituting the resin layer (4b) and has a weight average molecular weight Mw before crosslinking of 4500 or more. According to the present invention, the resin layer (4b) in which the effective line length SRlr is adjusted to 104% or less can be easily obtained, so that the developer (6) adheres to the surface of the developer carrier (4). The image density can be prevented from lowering. The developing device according to claim 6 (3).
Uses the developer carrier (4) according to any one of the first to fifth aspects of the present invention. Therefore, the same effects as those of the above-described inventions can be obtained.
【0017】[0017]
【実施例】以下、本発明を実施例によって具体的に説明
するが、本発明は下記の実施例に限定されるものではな
い。図2において、静電潜像保持体1は、負帯電系の有
機感光層を有する光導電性ドラムであって、帯電手段
(図示せず)により一様に帯電させた後、像光を照射す
ることによって生じる電位差により静電潜像2が形成さ
れる。静電潜像2が形成された時の表面電位は、例えば
画像部で−600V、画像形成時に白表示部となる背景
部で−120Vである。現像装置3は、上記像保持体1
に対向して配置された現像剤担持体4を備えている。現
像剤担持体4は、外径18mmおよび肉厚0.7mmの
円筒状アルミニウム製基体4aと、その周面上に導電性
微粒子が分散した樹脂層4bを有する。樹脂層4bは、
結着樹脂および希釈剤中に導電性微粒子を分散させた後
記の塗布液を基体4a上に塗布することによって形成さ
れた膜厚20μm程度の塗膜からなる。EXAMPLES Hereinafter, the present invention will be described specifically with reference to Examples, but the present invention is not limited to the following Examples. In FIG. 2, an electrostatic latent image holder 1 is a photoconductive drum having a negatively charged organic photosensitive layer, and is uniformly charged by a charging unit (not shown), and then irradiated with image light. The electrostatic latent image 2 is formed by the potential difference generated by the operation. The surface potential when the electrostatic latent image 2 is formed is, for example, −600 V in the image portion and −120 V in the background portion that becomes a white display portion during image formation. The developing device 3 includes the image carrier 1
And a developer carrier 4 disposed opposite to the developer carrier. The developer carrier 4 has a cylindrical aluminum base 4a having an outer diameter of 18 mm and a wall thickness of 0.7 mm, and a resin layer 4b in which conductive fine particles are dispersed on a peripheral surface thereof. The resin layer 4b
It is formed of a coating film having a thickness of about 20 μm formed by applying a coating liquid described later in which conductive fine particles are dispersed in a binder resin and a diluent, onto the substrate 4a.
【0018】現像容器5には、体積平均粒子径7μmの
磁性一成分現像剤6が充填される。また、この現像容器
5は、現像剤担持体4を収容すると共に、像保持体1に
対向して開口する部分で一部露出する担持体4表面と像
保持体1とが近接するように配置されている。容器5内
には、現像剤6を担持体4側に寄せるアジテータ(図示
せず)が回転自在に配置されている。現像剤担持体4
は、その回転により、表面に担持した現像剤6を像保持
体1と近接した現像領域に搬送する。現像領域における
担持体4と像保持体1との最小間隙は、200μm程度
となるように設定されている。担持体4の内部には、複
数の磁石が周面に沿って配列され、回転しないように固
定されたマグネットロール4cが設けられている。複数
の磁石はS極とN極とを周面に沿って配列した磁気パタ
ーンを形成しており、この磁気パターンに従って、現像
剤6を担持体4の表面に吸着することができるようにな
っている。The developing container 5 is filled with a magnetic one-component developer 6 having a volume average particle diameter of 7 μm. The developing container 5 accommodates the developer carrier 4 and is arranged so that the surface of the carrier 4 partially exposed at a portion opened to face the image carrier 1 is close to the image carrier 1. Have been. In the container 5, an agitator (not shown) for bringing the developer 6 toward the carrier 4 is rotatably arranged. Developer carrier 4
Transports the developer 6 carried on the surface to a development area close to the image holding member 1 by its rotation. The minimum gap between the carrier 4 and the image carrier 1 in the developing area is set to be about 200 μm. Inside the carrier 4, a plurality of magnets are arranged along a peripheral surface, and a magnet roll 4c fixed so as not to rotate is provided. The plurality of magnets form a magnetic pattern in which S poles and N poles are arranged along the peripheral surface. According to this magnetic pattern, the developer 6 can be attracted to the surface of the carrier 4. I have.
【0019】現像剤層厚規制部材7は、現像剤担持体4
表面に当接する弾性部材7aとこの弾性部材7aを接着
した板バネ7bとからなり、板バネ7bの他端は支持部
材を介して容器5の上壁に固定支持されている。弾性部
材7aは幅15mm、厚さ1.00mm、ゴム硬度65
゜のウレタンゴムからなり、板バネ7bは厚さ0.1m
mのステンレス鋼からなる。現像剤担持体4の基体4a
には、直列に接続した高圧交流電源および直流電源によ
ってバイアス電圧である直流重畳交流電圧が印加され、
像保持体1の導電性基体(図示せず)と基体4aの間で
交番電界が発生するようになっている。The developer layer thickness regulating member 7 includes a developer carrier 4
It comprises an elastic member 7a in contact with the surface and a leaf spring 7b to which the elastic member 7a is bonded. The other end of the leaf spring 7b is fixedly supported on the upper wall of the container 5 via a support member. The elastic member 7a has a width of 15 mm, a thickness of 1.00 mm, and a rubber hardness of 65.
ウ made of urethane rubber, leaf spring 7b is 0.1m thick
m of stainless steel. Substrate 4a of developer carrier 4
The DC superimposed AC voltage which is a bias voltage is applied by a high voltage AC power supply and a DC power supply connected in series,
An alternating electric field is generated between a conductive substrate (not shown) of the image carrier 1 and the substrate 4a.
【0020】本実施例の現像装置の作用は次のようなも
のである。容器5内の現像剤6は、現像剤担持体4の回
転によって、トナー粒子径より大きい凹凸と小さい凹凸
を有する樹脂層4b上に担持される。樹脂層4b上の現
像剤6は、現像剤層厚規制部材7を担持体4表面に付勢
する板バネ7bの押圧力により弾性部材7aで摺擦され
る。これにより、静電潜像2を現像するに適正な量の現
像剤6が担持体4上に薄層化されると同時に、現像剤6
に均一かつ充分な摩擦帯電電荷を付与することができ
る。薄層化された現像剤6は、担持体4の回転に伴って
現像領域に搬送され、担持体4と像保持体1との間隙に
発生する交番電界内で、帯電された現像剤6粒子が飛翔
して往復運動する。また、この往復運動によって、現像
剤6の粒子同士が衝突し現像剤6全体がクラウド状とな
る。この現像剤6のクラウドが、バイアス電圧の直流成
分によって、像保持体1の静電潜像2部分に引き寄せら
れて現像が終了する。The operation of the developing device according to the present embodiment is as follows. The developer 6 in the container 5 is carried on the resin layer 4 b having irregularities larger and smaller than the toner particle diameter by rotation of the developer carrier 4. The developer 6 on the resin layer 4b is rubbed by the elastic member 7a by the pressing force of the leaf spring 7b for urging the developer layer thickness regulating member 7 against the surface of the carrier 4. As a result, an appropriate amount of the developer 6 for developing the electrostatic latent image 2 is thinned on the carrier 4 and at the same time, the developer 6
A uniform and sufficient triboelectric charge can be imparted to the toner. The thinned developer 6 is conveyed to the developing area with the rotation of the carrier 4, and charged in the alternating electric field generated in the gap between the carrier 4 and the image carrier 1. Flies and reciprocates. In addition, the particles of the developer 6 collide with each other due to the reciprocating motion, and the entire developer 6 becomes cloud-like. The cloud of the developer 6 is attracted to the electrostatic latent image 2 of the image carrier 1 by the DC component of the bias voltage, and the development is completed.
【0021】実施例1 樹脂層(4b)の形成法を下記に示す。 結着樹脂 フェノール樹脂(前記Mw:4500) 100重量部 導電性微粒子 カーボンブラック(一次平均粒子径:10nm) 20重量部 グラファイト(体積平均粒子径:7.5〜9.0μm) 50重量部 希釈剤 プロピレングリコールモノメチルエーテル 100重量部 イソプロパノール 150重量部 上記組成からなる樹脂液中の導電性微粒子をサンドミル
で分散し、得られた塗布液をアルミニウム製基体(4a)
上にスプレーして塗布した後、熱乾燥炉において160
℃で30分間加熱硬化して樹脂層(4b)を形成した。こ
の樹脂層(4b)表面の算術平均粗さRaを前記触針式表
面粗さ測定機で測定したところ、1.7μmであった。
また、前記三次元表面形状解析装置により有効線長さSR
lrを求めたところ、103.4%であった。上記樹脂層
(4b)を被覆した基体(4a)の内部に前記マグネットロ
ール(4c)を固定し、このようにして現像剤担持体(4)
を作製した。Example 1 A method for forming the resin layer (4b) is described below. Binder resin Phenol resin (Mw: 4500) 100 parts by weight Conductive fine particles Carbon black (primary average particle diameter: 10 nm) 20 parts by weight Graphite (volume average particle diameter: 7.5 to 9.0 μm) 50 parts by weight Diluent Propylene glycol monomethyl ether 100 parts by weight Isopropanol 150 parts by weight The conductive fine particles in the resin liquid having the above composition are dispersed by a sand mill, and the obtained coating liquid is used as an aluminum substrate (4a).
After spraying and applying on top, 160
The resin was cured by heating at 30 ° C. for 30 minutes to form a resin layer (4b). The arithmetic average roughness Ra of the surface of the resin layer (4b) was measured by the stylus type surface roughness measuring instrument and found to be 1.7 μm.
In addition, the effective line length SR
The lr was found to be 103.4%. The above resin layer
The magnet roll (4c) is fixed inside the substrate (4a) coated with (4b), and thus the developer carrier (4) is fixed.
Was prepared.
【0022】以下実施例1とほぼ同様にして、実施例2
〜6および比較例1〜9の現像剤担持体を作製した。各
実施例および比較例には、実施例1に示した樹脂層の形
成法との相違、上記平均粗さRaおよび有効線長さSRlr
を示す。 実施例2 フェノール樹脂の架橋前の重量平均分子量Mwを480
0とした以外は、実施例1と同様にして樹脂層を形成し
た。この樹脂層表面の平均粗さRaは1.5μmであ
り、有効線長さSRlrは102.9%であった。 実施例3 フェノール樹脂の架橋前の重量平均分子量Mwを500
0とした以外は、実施例1と同様にして樹脂層を形成し
た。この樹脂層表面の平均粗さRaは1.3μmであ
り、有効線長さSRlrは102.5%であった。A second embodiment is substantially the same as the first embodiment.
To 6 and Comparative Examples 1 to 9 were prepared. In each of the examples and comparative examples, the difference from the method for forming the resin layer shown in the example 1, the average roughness Ra and the effective line length SRlr were described.
Is shown. Example 2 Weight average molecular weight Mw of phenol resin before crosslinking was 480
A resin layer was formed in the same manner as in Example 1 except that 0 was set. The average roughness Ra of the resin layer surface was 1.5 μm, and the effective line length SRlr was 102.9%. Example 3 Weight average molecular weight Mw of phenol resin before crosslinking was 500
A resin layer was formed in the same manner as in Example 1 except that 0 was set. The average roughness Ra of the resin layer surface was 1.3 μm, and the effective line length SRlr was 102.5%.
【0023】実施例4 実施例1と同様にして樹脂層を形成した。ただし、実施
例1とは、スプレー装置の回転数、吐出量、スプレーガ
ンと基体(4a)との距離を変化させた。形成された樹脂
層表面の平均粗さRaは1.8μmであり、有効線長さ
SRlrは103.5%であった。 実施例5 実施例1と同様にして樹脂層を形成した。ただし、実施
例1,4とは、スプレー装置の回転数、吐出量、スプレ
ーガンと基体との距離を変化させた。形成された樹脂層
表面の平均粗さRaは1.3μmであり、有効線長さSR
lrは103.0%であった。 実施例6 導電性微粒子として体積平均粒子径10μmのカーボン
ビーズ単独を40重量部用いた以外は、実施例1と同様
にして樹脂層を形成した。この樹脂層表面の平均粗さR
aは1.4μmであり、有効線長さSRlrは102.4%
であった。Example 4 A resin layer was formed in the same manner as in Example 1. However, in comparison with Example 1, the number of revolutions of the spray device, the discharge amount, and the distance between the spray gun and the base (4a) were changed. The average roughness Ra of the surface of the formed resin layer is 1.8 μm, and the effective line length is
SRlr was 103.5%. Example 5 A resin layer was formed in the same manner as in Example 1. However, in Examples 1 and 4, the number of revolutions of the spray device, the discharge amount, and the distance between the spray gun and the base were changed. The average roughness Ra of the formed resin layer surface is 1.3 μm, and the effective line length SR
lr was 103.0%. Example 6 A resin layer was formed in the same manner as in Example 1, except that only 40 parts by weight of carbon beads having a volume average particle diameter of 10 μm were used as the conductive fine particles. Average roughness R of this resin layer surface
a is 1.4 μm and the effective line length SRlr is 102.4%
Met.
【0024】比較例1 フェノール樹脂の架橋前の重量平均分子量Mwを400
0とした以外は、実施例1と同様にして樹脂層を形成し
た。この樹脂層表面の平均粗さRaは1.6μmであ
り、有効線長さSRlrは105.2%であった。 比較例2 フェノール樹脂の架橋前の重量平均分子量Mwを410
0とした以外は、実施例1と同様にして樹脂層を形成し
た。この樹脂層表面の平均粗さRaは1.5μmであ
り、有効線長さSRlrは104.8%であった。 比較例3 フェノール樹脂の架橋前の重量平均分子量Mwを430
0とした以外は、実施例1と同様にして樹脂層を形成し
た。この樹脂層表面の平均粗さRaは1.4μmであ
り、有効線長さSRlrは104.2%であった。Comparative Example 1 The weight average molecular weight Mw of the phenol resin before crosslinking was 400.
A resin layer was formed in the same manner as in Example 1 except that 0 was set. The average roughness Ra of the resin layer surface was 1.6 μm, and the effective line length SRlr was 105.2%. Comparative Example 2 The weight average molecular weight Mw of the phenol resin before crosslinking was 410
A resin layer was formed in the same manner as in Example 1 except that 0 was set. The average roughness Ra of the resin layer surface was 1.5 μm, and the effective line length SRlr was 104.8%. Comparative Example 3 Weight average molecular weight Mw of phenol resin before crosslinking was 430
A resin layer was formed in the same manner as in Example 1 except that 0 was set. The average roughness Ra of the resin layer surface was 1.4 μm, and the effective line length SRlr was 104.2%.
【0025】比較例4 フェノール樹脂の架橋前の重量平均分子量Mwを380
0とした以外は、実施例1と同様にして樹脂層を形成し
た。この樹脂層表面の平均粗さRaは1.4μmであ
り、有効線長さSRlrは106.2%であった。 比較例5 フェノール樹脂の架橋前の重量平均分子量Mwを300
0とした以外は、実施例1と同様にして樹脂層を形成し
た。この樹脂層表面の平均粗さRaは1.7μmであ
り、有効線長さSRlrは108.2%であった。 比較例6 実施例1と同様にして樹脂層を形成した。ただし、各実
施例とは、スプレー装置の回転数、吐出量、スプレーガ
ンと基体との距離を変化させた。形成された樹脂層表面
の平均粗さRaは2.0μmであり、有効線長さSRlrは
103.5%であった。Comparative Example 4 The weight average molecular weight Mw of the phenolic resin before crosslinking was 380
A resin layer was formed in the same manner as in Example 1 except that 0 was set. The average roughness Ra of the resin layer surface was 1.4 μm, and the effective line length SRlr was 106.2%. Comparative Example 5 Weight average molecular weight Mw of phenol resin before crosslinking was 300
A resin layer was formed in the same manner as in Example 1 except that 0 was set. The average roughness Ra of the resin layer surface was 1.7 μm, and the effective line length SRlr was 108.2%. Comparative Example 6 A resin layer was formed in the same manner as in Example 1. However, the number of revolutions of the spray device, the discharge amount, and the distance between the spray gun and the base were changed from those of the examples. The average roughness Ra of the surface of the formed resin layer was 2.0 μm, and the effective line length SRlr was 103.5%.
【0026】比較例7 実施例1と同様にして樹脂層を形成した。ただし、各実
施例および比較例6とは、スプレー装置の回転数、吐出
量、スプレーガンと基体との距離を変化させた。形成さ
れた樹脂層表面の平均粗さRaは1.1μmであり、有
効線長さSRlrは103.3%であった。 比較例8 カーボンビーズの使用量を50重量部とした以外は、実
施例6と同様にして樹脂層を形成した。この樹脂層表面
の平均粗さRaは2.1μmであり、有効線長さSRlrは
102.9%であった。 比較例9 カーボンビーズの使用量を20重量部とした以外は、実
施例6と同様にして樹脂層を形成した。この樹脂層表面
の平均粗さRaは1.0μmであり、有効線長さSRlrは
102.7%であった。Comparative Example 7 A resin layer was formed in the same manner as in Example 1. However, in each of Examples and Comparative Example 6, the number of revolutions of the spray device, the discharge amount, and the distance between the spray gun and the base were changed. The average roughness Ra of the surface of the formed resin layer was 1.1 μm, and the effective line length SRlr was 103.3%. Comparative Example 8 A resin layer was formed in the same manner as in Example 6, except that the amount of carbon beads used was changed to 50 parts by weight. The average roughness Ra of the resin layer surface was 2.1 μm, and the effective line length SRlr was 102.9%. Comparative Example 9 A resin layer was formed in the same manner as in Example 6, except that the amount of carbon beads used was changed to 20 parts by weight. The average roughness Ra of the resin layer surface was 1.0 μm, and the effective line length SRlr was 102.7%.
【0027】以上の算術平均粗さRaおよび有効線長さ
SRlrを下記の表1にまとめて示す。更に、実施例1〜5
および比較例1〜7において、樹脂層(4b)中のカーボ
ンブラックの二次粒子径R1 (μm)、およびサンドミル
で分散した直後の塗布液中のグラファイトの粒子径R2
(μm)を測定した。得られた粒子径およびフェノール樹
脂1g当たりのトナー粒子径より小さいカーボンブラッ
クの含有量V1(0.2g)とトナー粒子径より大きいグ
ラファイトの含有量V2(0.5g)を前記式に代入し
て、導電性微粒子の粒子径と結着樹脂中の含有量の関係
を表す数値を求めた。それらの結果を表1に示す。表1
に示すように、有効線長さSRlrが104%以下の場合、
前記粒子径と含有量の関係を表す式に従って算出された
数値は全て300未満であった。The above arithmetic mean roughness Ra and effective line length
SRlr is summarized in Table 1 below. Further, Examples 1 to 5
In Comparative Examples 1 to 7, the secondary particle diameter R 1 (μm) of carbon black in the resin layer (4b) and the particle diameter R 2 of graphite in the coating solution immediately after being dispersed by a sand mill were used.
(μm) was measured. The obtained particle diameter, the content V 1 (0.2 g) of carbon black smaller than the toner particle diameter and the content V 2 (0.5 g) of graphite larger than the toner particle diameter per 1 g of the phenol resin are substituted into the above equations. Then, a numerical value representing the relationship between the particle size of the conductive fine particles and the content in the binder resin was determined. Table 1 shows the results. Table 1
As shown in the figure, when the effective line length SRlr is 104% or less,
Numerical values calculated according to the equation representing the relationship between the particle diameter and the content were all less than 300.
【0028】[0028]
【表1】 [Table 1]
【0029】(コピーテスト)実施例1〜6および比較
例1〜9で作製した現像剤担持体(4)をデジタル複写機
(Able1320:富士ゼロックス社製)に組み込
み、高温高湿(30℃,RH85%)下にコピーテスト
を行った。得られたコピーサンプルにおいて、初期画像
濃度とプリント枚数1000枚後の画像濃度は、濃度計
(Model404A:X−Rite社製)で測定し
た。画像濃度の低下率は、初期画像濃度に対する100
0枚後の濃度低下の割合を百分率で算出した。また、細
線太りは、幅100μmの直線を複写した後に光学顕微
鏡の観察結果から評価し、直線の幅が135μm未満の
ものを良好(○)とし、135μm以上のものを不良
(×)とした。「現像剤固着」は、プリント枚数100
0枚の時点で、現像剤担持体への現像剤の固着の有無を
目視によって評価した。それらの結果を表2に示す。現
像剤固着の評価○ : 固着なし× : 固着あり(Copy Test) The developer carrier (4) prepared in Examples 1 to 6 and Comparative Examples 1 to 9 was incorporated in a digital copying machine (Able 1320: manufactured by Fuji Xerox Co., Ltd.), RH 85%). In the obtained copy sample, the initial image density and the image density after 1000 prints were measured with a densitometer (Model 404A: manufactured by X-Rite). The reduction rate of the image density is 100% of the initial image density.
The ratio of the decrease in density after 0 sheets was calculated as a percentage. The thickening of the thin line was evaluated from the result of observation with an optical microscope after copying a straight line having a width of 100 μm. "Developer fixation" means that the number of prints is 100
At the time of 0 sheets, the presence or absence of the developer fixed to the developer carrying member was visually evaluated. Table 2 shows the results. Evaluation of developer sticking ○: No sticking ×: Sticking
【0030】[0030]
【表2】 [Table 2]
【0031】各実施例の現像剤担持体では、初期画像濃
度、1000枚後の画像濃度の低下率、細線太りおよび
現像剤固着とも、実用上問題のない結果が得られた。一
方、算術平均粗さRaが1.3〜1.8μmの範囲外にあ
るか、あるいは有効線長さSRlrが104%より大きい各
比較例の現像剤担持体では、何らかの画像欠陥が生じ
た。すなわち、平均粗さRaが1.3μm未満の場合
は、現像剤の搬送量不足から現像に必要な現像剤量が足
りず、結果的に初期画像濃度が低下した。平均粗さRa
が1.8μmより大きい場合は、現像剤量過多による細
線の太りが生じた。また、有効線長さSRlrが104%よ
り大きいと、現像剤担持体への現像剤の固着が生じるた
め、1000枚プリント後の画像濃度の低下が大きかっ
た。With the developer carrying member of each of the examples, practically satisfactory results were obtained with respect to the initial image density, the reduction rate of the image density after 1000 sheets, the thickening of the fine line, and the fixing of the developer. On the other hand, in the developer carrying member of each comparative example in which the arithmetic average roughness Ra is out of the range of 1.3 to 1.8 μm or the effective line length SRlr is more than 104%, some image defects occurred. That is, when the average roughness Ra was less than 1.3 μm, the amount of the developer required for development was insufficient due to the shortage of the amount of the developer transported, and as a result, the initial image density was reduced. Average roughness Ra
Is larger than 1.8 μm, the thickness of the thin line was increased due to an excessive amount of the developer. Further, when the effective line length SRlr is larger than 104%, the developer adheres to the developer carrier, so that the image density after printing 1,000 sheets has been greatly reduced.
【0032】以上の実施例および比較例の結果をグラフ
化したものが図3,4である。図3は現像剤担持体表面
の算術平均粗さRaと有効線長さSRlrのウィンドウを示
したグラフであり、枠で囲んだ部分が本発明の実施例を
示す。図4は現像剤担持体表面の有効線長さSRlrと画像
濃度の低下率の関係を示し、図中の数字は比較例の番号
を示す。図4からも明らかなように、現像剤担持体表面
の有効線長さSRlrが104%以下の場合は、画像濃度が
全くまたはほとんど低下しない。これは、現像剤担持体
への現像剤の固着が回避されていることを意味する。FIGS. 3 and 4 are graphs showing the results of the above Examples and Comparative Examples. FIG. 3 is a graph showing a window of the arithmetic mean roughness Ra and the effective line length SRlr of the surface of the developer carrier, and a portion surrounded by a frame indicates an embodiment of the present invention. FIG. 4 shows the relationship between the effective line length SRlr on the surface of the developer carrying member and the reduction rate of the image density, and the numbers in the figure show the numbers of comparative examples. As is apparent from FIG. 4, when the effective line length SRlr of the surface of the developer carrying member is 104% or less, the image density does not decrease at all or hardly. This means that sticking of the developer to the developer carrier is avoided.
【0033】[0033]
【発明の効果】本発明の現像剤担持体および現像装置に
よれば、樹脂層表面におけるトナー粒子径より大きい凹
凸が算術平均粗さRaで1.3〜1.8μmの範囲にあ
り、かつトナー粒子径より小さい凹凸が有効線長さSRlr
で104%以下であるため、画像濃度が適正であって細
線太りがなく、しかも現像剤担持体への現像剤の固着を
回避することが可能となった。According to the developer carrier and the developing device of the present invention, the irregularities larger than the toner particle diameter on the surface of the resin layer are in the range of 1.3 to 1.8 μm in arithmetic average roughness Ra, and the toner The irregularity smaller than the particle diameter is the effective line length SRlr
And 104% or less, the image density was appropriate, the fine line was not thickened, and the sticking of the developer to the developer carrier could be avoided.
【図1】 現像剤担持体の表面粗さの指標として有効線
長さSRlrを説明するために示した樹脂層表面の微小な凹
凸形状の拡大断面図である。FIG. 1 is an enlarged cross-sectional view of a minute uneven shape on the surface of a resin layer for explaining an effective line length SRlr as an index of a surface roughness of a developer carrying member.
【図2】 本発明の一実施例として示す一成分現像装置
の説明図である。FIG. 2 is an explanatory diagram of a one-component developing device shown as one embodiment of the present invention.
【図3】 現像剤担持体表面の算術平均粗さRaと有効
線長さSRlrのウィンドウを示すグラフである。FIG. 3 is a graph showing a window of an arithmetic mean roughness Ra and an effective line length SRlr of the surface of a developer carrying member.
【図4】 現像剤担持体表面の有効線長さSRlrと画像濃
度の低下率の関係を示すグラフである。FIG. 4 is a graph showing the relationship between the effective line length SRlr on the surface of a developer carrying member and the rate of decrease in image density.
1…静電潜像保持体,2…静電潜像,3…現像装置,4
…現像剤担持体,4a…円筒状基体,4b…樹脂層,5
…現像容器,6…現像剤,7…現像剤層厚規制部材。DESCRIPTION OF SYMBOLS 1 ... Electrostatic latent image holding body, 2 ... Electrostatic latent image, 3 ... Developing device, 4
... developer carrier, 4a ... cylindrical substrate, 4b ... resin layer, 5
... developer container, 6 ... developer, 7 ... developer layer thickness regulating member.
Claims (6)
る樹脂層が円筒状基体の外周面に被覆され、樹脂層表面
にはトナー粒子径より大きい凹凸とトナー粒子径より小
さい凹凸が形成され、トナー粒子径より大きい凹凸が算
術平均粗さRaで1.3〜1.8μmの範囲にあり、かつ
トナー粒子径より小さい凹凸が有効線長さSRlrで1
04%以下であることを特徴とする現像剤担持体。1. A resin layer comprising a binder resin containing conductive fine particles is coated on the outer peripheral surface of a cylindrical substrate, and irregularities larger than the toner particle diameter and irregularities smaller than the toner particle diameter are formed on the surface of the resin layer. The unevenness larger than the toner particle diameter is in the range of 1.3 to 1.8 μm in arithmetic average roughness Ra, and the unevenness smaller than the toner particle diameter is 1 in the effective line length SRlr.
A developer carrying member having a content of not more than 04%.
きい請求項1記載の現像剤担持体。2. The developer carrier according to claim 1, wherein the conductive fine particles are larger than a toner particle diameter.
導電性微粒子とトナー粒子径より小さい導電性微粒子と
を同時に含有する請求項1記載の現像剤担持体。3. The developer carrier according to claim 1, wherein the resin layer simultaneously contains conductive fine particles larger than the toner particle diameter and conductive fine particles smaller than the toner particle diameter.
樹脂中の含有量が下記の式で表される関係を満す請求項
3記載の現像剤担持体。 4.5×103×(R1)3V1 + (R2)3V2 < 300 式中、R1 ,V1 ,R2 ,V2 は下記の粒子径または含
有量を意味する。 R1 :トナー粒子径より小さい導電性微粒子の二次粒子
径(μm) V1 :トナー粒子径より小さい導電性微粒子の含有量
(g)/g(結着樹脂) R2 :トナー粒子径より大きい導電性微粒子の分散後の
粒子径(μm) V2 :トナー粒子径より大きい導電性微粒子の含有量
(g)/g(結着樹脂)4. The developer carrier according to claim 3, wherein the particle diameter of each of the conductive fine particles and the content in the binder resin satisfy a relationship represented by the following formula. 4.5 × 10 3 × (R 1 ) 3 V 1 + (R 2 ) 3 V 2 <300 In the formula, R 1 , V 1 , R 2 and V 2 mean the following particle diameters or contents. R 1 : secondary particle diameter (μm) of conductive fine particles smaller than toner particle diameter V 1 : content of conductive fine particles smaller than toner particle diameter
(g) / g (binder resin) R 2 : particle size after dispersion of conductive fine particles larger than toner particle size (μm) V 2 : content of conductive fine particles larger than toner particle size
(g) / g (binder resin)
該フェノール樹脂の架橋前の重量平均分子量が4500
以上である請求項1〜4のいずれかに記載の現像剤担持
体。5. The binder resin is a phenol resin,
The phenol resin has a weight average molecular weight of 4500 before crosslinking.
The developer carrier according to any one of claims 1 to 4, which is as described above.
像剤担持体上に担持して、現像剤担持体上の現像剤を現
像剤層厚規制部材により均一な厚みに規制し、静電潜像
保持体と現像剤担持体の間に電界を作用させて、現像剤
により静電潜像保持体表面の静電潜像を現像する現像装
置において、上記現像剤担持体として請求項1〜5に記
載のいずれか1つを用いることを特徴とする現像装置。6. A developer carrying a one-component developer filled in a developing container on a developer carrier, and regulating the developer on the developer carrier to a uniform thickness by a developer layer thickness regulating member. 2. A developing device for developing an electrostatic latent image on a surface of an electrostatic latent image holding member with a developer by applying an electric field between the electrostatic latent image holding member and the developer holding member, wherein the developer holding member is used as the developer holding member. A developing device using any one of the above-described items.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5503197A JP3671579B2 (en) | 1996-07-26 | 1997-03-10 | Developer carrying member and developing device using the same |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19741196 | 1996-07-26 | ||
| JP8-197411 | 1996-07-26 | ||
| JP5503197A JP3671579B2 (en) | 1996-07-26 | 1997-03-10 | Developer carrying member and developing device using the same |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH1090995A true JPH1090995A (en) | 1998-04-10 |
| JP3671579B2 JP3671579B2 (en) | 2005-07-13 |
Family
ID=26395864
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5503197A Expired - Fee Related JP3671579B2 (en) | 1996-07-26 | 1997-03-10 | Developer carrying member and developing device using the same |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3671579B2 (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6493522B2 (en) * | 2000-06-09 | 2002-12-10 | Canon Kabushiki Kaisha | Developing device and image forming apparatus |
| JP2006267949A (en) * | 2005-03-25 | 2006-10-05 | Fuji Xerox Co Ltd | Developing device and image forming apparatus |
| JP2007121567A (en) * | 2005-10-26 | 2007-05-17 | Fuji Xerox Co Ltd | Developing device and image forming apparatus using same |
| JP2008040400A (en) * | 2006-08-10 | 2008-02-21 | Fuji Xerox Co Ltd | Development device, image forming apparatus using the same, developer carrier, and method for producing the same |
-
1997
- 1997-03-10 JP JP5503197A patent/JP3671579B2/en not_active Expired - Fee Related
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6493522B2 (en) * | 2000-06-09 | 2002-12-10 | Canon Kabushiki Kaisha | Developing device and image forming apparatus |
| JP2006267949A (en) * | 2005-03-25 | 2006-10-05 | Fuji Xerox Co Ltd | Developing device and image forming apparatus |
| JP2007121567A (en) * | 2005-10-26 | 2007-05-17 | Fuji Xerox Co Ltd | Developing device and image forming apparatus using same |
| JP2008040400A (en) * | 2006-08-10 | 2008-02-21 | Fuji Xerox Co Ltd | Development device, image forming apparatus using the same, developer carrier, and method for producing the same |
Also Published As
| Publication number | Publication date |
|---|---|
| JP3671579B2 (en) | 2005-07-13 |
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