JPH03129368A - Developing device - Google Patents
Developing deviceInfo
- Publication number
- JPH03129368A JPH03129368A JP1266321A JP26632189A JPH03129368A JP H03129368 A JPH03129368 A JP H03129368A JP 1266321 A JP1266321 A JP 1266321A JP 26632189 A JP26632189 A JP 26632189A JP H03129368 A JPH03129368 A JP H03129368A
- Authority
- JP
- Japan
- Prior art keywords
- toner
- surfactant
- developing device
- layer
- rubber
- 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
- 229920005989 resin Polymers 0.000 claims abstract description 19
- 239000011347 resin Substances 0.000 claims abstract description 19
- 239000004094 surface-active agent Substances 0.000 claims abstract description 17
- 239000002563 ionic surfactant Substances 0.000 claims abstract description 4
- 239000011737 fluorine Substances 0.000 claims description 14
- 229910052731 fluorine Inorganic materials 0.000 claims description 14
- 230000001105 regulatory effect Effects 0.000 claims description 3
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- -1 ester compounds Chemical class 0.000 abstract description 18
- 206010047571 Visual impairment Diseases 0.000 abstract description 12
- 239000003093 cationic surfactant Substances 0.000 abstract description 6
- 238000005299 abrasion Methods 0.000 abstract description 5
- 239000003945 anionic surfactant Substances 0.000 abstract description 5
- 125000002091 cationic group Chemical group 0.000 abstract description 5
- 239000002280 amphoteric surfactant Substances 0.000 abstract description 4
- 125000000129 anionic group Chemical group 0.000 abstract description 4
- 235000014113 dietary fatty acids Nutrition 0.000 abstract description 3
- 239000000194 fatty acid Substances 0.000 abstract description 3
- 229930195729 fatty acid Natural products 0.000 abstract description 3
- 150000004665 fatty acids Chemical class 0.000 abstract description 3
- 150000002170 ethers Chemical class 0.000 abstract description 2
- 125000003368 amide group Chemical group 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 34
- 238000000034 method Methods 0.000 description 20
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 13
- 229920001971 elastomer Polymers 0.000 description 9
- 239000005060 rubber Substances 0.000 description 9
- 239000007787 solid Substances 0.000 description 8
- 108091008695 photoreceptors Proteins 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- 230000007613 environmental effect Effects 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 125000005010 perfluoroalkyl group Chemical group 0.000 description 5
- 229920001296 polysiloxane Polymers 0.000 description 5
- 239000004594 Masterbatch (MB) Substances 0.000 description 4
- 229920002379 silicone rubber Polymers 0.000 description 4
- 239000004945 silicone rubber Substances 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000006229 carbon black Substances 0.000 description 3
- 239000011247 coating layer Substances 0.000 description 3
- 230000003247 decreasing effect Effects 0.000 description 3
- 229920005558 epichlorohydrin rubber Polymers 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 235000021317 phosphate Nutrition 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000008096 xylene Substances 0.000 description 3
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- 239000004709 Chlorinated polyethylene Substances 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
- 229920000459 Nitrile rubber Polymers 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 229920000800 acrylic rubber Polymers 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229920006026 co-polymeric resin Polymers 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 239000013013 elastic material Substances 0.000 description 2
- 230000008030 elimination Effects 0.000 description 2
- 238000003379 elimination reaction Methods 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000011256 inorganic filler Substances 0.000 description 2
- 229910003475 inorganic filler Inorganic materials 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- 229920001084 poly(chloroprene) Polymers 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 239000010453 quartz Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 150000003871 sulfonates Chemical class 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- 238000004073 vulcanization Methods 0.000 description 2
- PSBDWGZCVUAZQS-UHFFFAOYSA-N (dimethylsulfonio)acetate Chemical compound C[S+](C)CC([O-])=O PSBDWGZCVUAZQS-UHFFFAOYSA-N 0.000 description 1
- 229910052582 BN Inorganic materials 0.000 description 1
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical compound NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 229920002943 EPDM rubber Polymers 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 229920006311 Urethane elastomer Polymers 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- 239000003082 abrasive agent Substances 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 125000005599 alkyl carboxylate group Chemical group 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 150000001449 anionic compounds Chemical class 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 239000000981 basic dye Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- VNWKTOKETHGBQD-YPZZEJLDSA-N carbane Chemical group [10CH4] VNWKTOKETHGBQD-YPZZEJLDSA-N 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical class OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 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
- 238000007598 dipping method Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- LMHDQOWNISVSPD-UHFFFAOYSA-N fluorine(1+) Chemical compound [F+] LMHDQOWNISVSPD-UHFFFAOYSA-N 0.000 description 1
- 229920001973 fluoroelastomer Polymers 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000000314 lubricant Substances 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
- 239000007769 metal material Substances 0.000 description 1
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 description 1
- 239000000113 methacrylic resin Substances 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229920005792 styrene-acrylic resin Polymers 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229940117986 sulfobetaine Drugs 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Landscapes
- Dry Development In Electrophotography (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野コ
本発明は、−成分系トナーを用いる静電潜像の現像装置
に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to an electrostatic latent image developing device using a -component toner.
[従来の技術]
従来、非磁性−成分トナーを用いて静電潜像を現像する
方法として、トナー担持体(即ち現像ローラ)上のトナ
ーをブレード状あるいはロール状の部材により薄層化し
、これを静電潜像を保持した保持体(即ち感光体)上に
当接して現像する方法が知られている。この方法におい
ては現像ローラは、■トナーの補給■トナーの帯電■ト
ナーの薄層形成■トナーの搬送■現像■残留電荷の除電
等のサイクルを繰り返すのであるが、現像ローラが−サ
イクルし、次のサイクルに入る場合に現像ローラにはト
ナーとの摩擦帯電によってカウンターチャージが生じた
り、感光体からの分配電荷がその表面や内部に残存する
ため繰り返しの使用によってトナーの帯電特性や現像特
性が劣化し、いわゆる残像現像が生じるといった難点が
あった。[Prior Art] Conventionally, as a method for developing an electrostatic latent image using a non-magnetic component toner, the toner on a toner carrier (i.e., a developing roller) is made into a thin layer using a blade-shaped or roll-shaped member, and then A method is known in which the electrostatic latent image is brought into contact with a holder (i.e., a photoreceptor) holding an electrostatic latent image for development. In this method, the developing roller repeats the following cycles: ■ Replenishing toner ■ Charging the toner ■ Forming a thin layer of toner ■ Transporting the toner ■ Developing ■ Eliminating residual charges. When the developing roller enters the cycle, a counter charge occurs due to frictional charging with the toner, and the distributed charge from the photoreceptor remains on its surface or inside, so the charging characteristics and development characteristics of the toner deteriorate with repeated use. However, there was a problem that so-called afterimage development occurred.
このため、従来より現像ローラの除電方法が色々検討さ
れており、例えばトナー担持体の表面に金属ブラシや導
電性スポンジなどの低抵抗体を当接する方法が提案され
ている。For this reason, various methods of neutralizing the developing roller have been studied, and for example, a method has been proposed in which a low-resistance member such as a metal brush or a conductive sponge is brought into contact with the surface of the toner carrier.
しかしながら、金属ブラシを用いる方法は、トナー担持
体表面への当接が不均一であるため、画像上にスジ状の
シマが出てしまう場合があり、又導電性スポンジを用い
る方法はその残像消失効果が充分ではなかった。更に、
これらの方法はトナー薄層を介してトナー担持体に当接
する方法であることから、除電効果が極めて悪いといっ
た欠点があった。又、除電効果を向上させるために、ブ
ラシの材質や密度、スポンジロールの設置本数の検討な
ど種々な試みがなされているが、残像を完全に消失する
までに至らなかった。一方、こういった現像システム側
からの改良により、非常に初期化され易い、換言すれば
電荷が残存しない現像ローラの開発もなされている。However, the method using a metal brush may cause streaks to appear on the image due to uneven contact with the surface of the toner carrier, and the method using a conductive sponge eliminates the afterimage. The effect was not sufficient. Furthermore,
Since these methods contact the toner carrier through a thin layer of toner, they have the disadvantage that the static elimination effect is extremely poor. In addition, various attempts have been made to improve the static elimination effect, such as examining the material and density of the brush and the number of sponge rolls installed, but it has not been possible to completely eliminate the afterimage. On the other hand, as a result of these improvements from the developing system side, developing rollers that are very easy to initialize, in other words, no charge remains, have been developed.
このような現像ローラとしては、例えば第一被覆層の導
電性基体としてtOS〜IQIIΩ・elNの中程度の
体積抵抗(以下、中抵抗)の弾性材料を用い、その上に
第2被覆層として可撓性の合成樹脂と導電粒子とからな
る半導電性体で被覆しである現像ローラがある。しかし
このものは使用する材料がアクリロニトリルブタジェン
ゴム、エピクロルヒドリンゴム、クロロブレンゴム、ウ
レタンゴム等であるため、均一で安定したものを作るこ
とが困難であり、特に電気特性の耐環境性(熱とか湿度
)が劣っており、そのため環境条件により現像特性が変
化するという欠点を有する。For such a developing roller, for example, an elastic material with a medium volume resistivity (hereinafter referred to as medium resistance) of tOS to IQIIΩ·elN is used as the conductive base of the first coating layer, and a conductive substrate is used as the second coating layer thereon. There is a developing roller coated with a semiconductive material made of flexible synthetic resin and conductive particles. However, since the materials used for this product are acrylonitrile butadiene rubber, epichlorohydrin rubber, chloroprene rubber, urethane rubber, etc., it is difficult to make a uniform and stable product, and it is particularly difficult to make a uniform and stable product with environmental resistance such as electrical properties (heat, etc.). It has the disadvantage that the development characteristics change depending on the environmental conditions.
一方、106Ω・C11以下の体積抵抗を保有する導電
性弾性体を用い、その上に中抵抗−高抵抗領域の樹脂又
はゴム層を、ついで電極層を順次積層した現像ローラが
提案されている。このものは各層に耐熱・耐湿性の優れ
た樹脂又はゴム(例えば、シリコーン系、フッ素系ポリ
マー)を用いることにより耐環境性を著しく向上できる
という利点を有する。On the other hand, a developing roller has been proposed in which a conductive elastic body having a volume resistivity of 106 Ω·C11 or less is used, a resin or rubber layer in the medium to high resistance range is sequentially laminated thereon, and then an electrode layer is laminated thereon. This product has the advantage that environmental resistance can be significantly improved by using resin or rubber (eg, silicone type, fluorine type polymer) with excellent heat resistance and moisture resistance in each layer.
しかしながら、この現像ローラは被覆層として中抵抗−
高抵抗樹脂を用いているために、トナーとの摩擦帯電プ
ロセスによって生じた帯電電荷が残留蓄積し、次工程に
おけるトナー帯電性や現像特性に大きな影響を与え、残
像を生じるという欠点を有する。又、当該現像ローラの
電極層に、導電粒子を分散させ低抵抗化させることによ
って電荷リークを促進する試みもなされているが、電荷
をリークさせる程度の導電性を表面層に付与した場合
■ トナーの帯1!量及びトナーの搬送性の低下■ 表
面層の低抵抗化に伴う保持体との電界強度の増加による
濃度過多、解像度の低下■ 多量の導電粒子添加による
表面層の対トナーのM型性の低下やトナーフィルミング
の発生耐摩耗性の低下
などの問題が生じ、全ての面において満足すべき現像ロ
ーラが開発されていないのが現状である。However, this developing roller has a medium resistance as a coating layer.
Since a high-resistance resin is used, residual charges generated by the frictional charging process with the toner remain and accumulate, which greatly affects toner chargeability and development characteristics in the next step, resulting in an afterimage. In addition, attempts have been made to promote charge leakage by dispersing conductive particles in the electrode layer of the developing roller to lower the resistance. Obi 1! Decreased amount and toner transportability■ Excessive concentration and decreased resolution due to increased electric field strength with the holder due to lower resistance of the surface layer■ Decreased M-type property of the surface layer for toner due to the addition of a large amount of conductive particles Problems such as occurrence of toner filming and reduction in abrasion resistance occur, and the current situation is that a developing roller that is satisfactory in all aspects has not been developed.
[発明が解決しようとする課題]
本発明は、上記従来技術の実情に鑑みてなされたもので
あって、トナーの帯電性及び離型性に優れ、長期間繰り
返し使用しても残像を生じることかなく、シかも耐久性
に優れ低コストで小型化の可能なトナー担持体及び該ト
ナー担持体を用いた現像装置を提供することを目的とす
る。[Problems to be Solved by the Invention] The present invention has been made in view of the above-mentioned actual state of the prior art, and the toner has excellent chargeability and releasability, and does not cause afterimages even after repeated use over a long period of time. It is an object of the present invention to provide a toner carrier that has excellent durability, is low cost, and can be downsized, and a developing device using the toner carrier.
[課題を解決するための手段]
本発明者らは、前記した課題を解決するため鋭意検討し
た結果、トナー担持体に界面活性剤を含有する樹脂層を
設けることが有効であることを見出し、本発明に至った
。[Means for Solving the Problems] As a result of intensive studies to solve the above-mentioned problems, the present inventors found that it is effective to provide a resin layer containing a surfactant on a toner carrier, This led to the present invention.
すなわち、本発明は、少なくとも静電潜像を保持する静
電潜像保持体、該保持体に潜像を顕像化せしめるトナー
担持体、及び該トナー担持体上にトナーの薄層を形成せ
しめる規制部材からなる現像装置において、前記トナー
担持体に界面活性剤を含有する樹脂層を設けた現像装置
である。That is, the present invention provides at least an electrostatic latent image holder that holds an electrostatic latent image, a toner carrier that makes the latent image visible on the holder, and a thin layer of toner that is formed on the toner carrier. The developing device includes a regulating member in which a resin layer containing a surfactant is provided on the toner carrier.
本発明の現像装置を第1図に沿って説明する。The developing device of the present invention will be explained with reference to FIG.
第1図においては、1は容器、2はトナー、3はアジテ
ータ 4は補給ローラ、5は例えば現像ローラの様なト
ナー担持体、6は規制部材としてのトナー薄層ブレード
、7は例えば感光体ドラムのような静電潜像保持体であ
る。In FIG. 1, 1 is a container, 2 is a toner, 3 is an agitator, 4 is a supply roller, 5 is a toner carrier such as a developing roller, 6 is a toner thin layer blade as a regulating member, and 7 is a photoreceptor, for example. It is a drum-like electrostatic latent image holder.
第1図において、トナー容器lの中に非磁性の一成分ト
ナー2が入っている。このトナー2はアジテータ 3に
よって、補給ローラ 4とトナー担持体5により形成さ
れるトナー貯留部に搬送され、トナー担持体5の表面に
担持される。In FIG. 1, a non-magnetic monocomponent toner 2 is contained in a toner container l. This toner 2 is conveyed by an agitator 3 to a toner storage section formed by a supply roller 4 and a toner carrier 5, and is carried on the surface of the toner carrier 5.
さらにトナー薄層ブレードBによって均一な薄層を形成
すると共に所定の極性に摩擦帯電される。トナー薄層は
、静電潜像を保持する保持体7とトナー担持体5とが当
接する現像領域に運ばれ、ここでトナー担持体から保持
体7ヘトナーが静電的に移行し、潜像が顕像化される。Furthermore, a uniform thin layer is formed by the toner thin layer blade B, and the toner is triboelectrically charged to a predetermined polarity. The thin toner layer is carried to a development area where the holder 7 holding the electrostatic latent image and the toner carrier 5 are in contact with each other, where the toner is electrostatically transferred from the toner carrier to the holder 7, forming the latent image. is visualized.
以上のプロセスにおいて、トナー2とトナー担持体5と
は摩擦帯電によって静電的に結合しているが、このトナ
ー2が保持体7に移動した後に、トナー担持体5中には
、カウンターチャージが残存し、いわゆる残像現像を生
じる。In the above process, the toner 2 and the toner carrier 5 are electrostatically bonded by frictional charging, but after the toner 2 moves to the holder 7, a counter charge is generated in the toner carrier 5. The residual image remains behind, causing so-called afterimage development.
本発明はこのようなカウンターチャージを迅速にリーク
し、かつトナーの帯電性、搬送性、離型性等を改良する
ために、前述の如き特定構造のトナー担持体を用いる。The present invention uses a toner carrier having a specific structure as described above in order to quickly leak such countercharge and improve toner charging properties, transport properties, mold release properties, etc.
なお、本発明は上述のごとく非磁性−成分現像のトナー
担持体にだけでなく、磁性−成分現像の現像ローラにも
適用できる。更に、形状ローラ状のものに限らず、例え
ばベルト状のようなものでも良い。又静電潜像保持体も
感光体に限らず、静電潜像を保持し得る部材であれば良
い。The present invention is applicable not only to the toner carrier for non-magnetic component development as described above, but also to the developing roller for magnetic component development. Further, the shape is not limited to a roller-like shape, but may be a belt-like shape, for example. Further, the electrostatic latent image holder is not limited to a photoreceptor, and may be any member that can hold an electrostatic latent image.
第2図に本発明で用いるトナー担持体を示す。FIG. 2 shows a toner carrier used in the present invention.
芯金23上に導電性弾性層22、樹脂層21を順次設け
た構成のものである。It has a structure in which a conductive elastic layer 22 and a resin layer 21 are sequentially provided on a core bar 23.
芯金23は従来公知の材料、例えばステンレス、アルミ
ニウム、鉄などの金属材料によって形成される。The core metal 23 is made of a conventionally known material, for example, a metal material such as stainless steel, aluminum, or iron.
導電性弾性層22は、本発明内で用いる第1図の現像装
置のような感光体ドラムとの接触現像においては現像ロ
ーラの弾性が要求されるため設けられるが、感光体がベ
ルト状などの場合、この層はなくてもよい。この層は対
向電極として機能させるために、1O12Ω・8m以下
の体積固有抵抗を有する導電性弾性体を用いることが望
ましい。The conductive elastic layer 22 is provided because elasticity of the developing roller is required in contact development with a photoreceptor drum as in the developing device shown in FIG. 1 used in the present invention. In this case, this layer may be omitted. In order for this layer to function as a counter electrode, it is desirable to use a conductive elastic material having a volume resistivity of 1O12Ω.8 m or less.
この場合、スチレン−ブタジェンゴム、エピクロルヒド
リンゴム、アクリルゴム、クロロブレンゴム等の有極性
ゴムやシリコーンゴム、EPDM、フッ素ゴム等の高抵
抗ゴムにカーボンなどの低抵抗粒子を分散したものが用
いられるが、可塑剤等を用いなくても低高度化が可能な
シリコーンゴムが特に好ましく使用される。これらの材
料はプレス成形、射出成形、押し出し成形等の通常の成
形手段によって得ることができ、更に研磨によって所定
形状のものとすることができる。この導電性弾性層の膜
厚は充分な弾性効果を発揮させるために1mm以上とす
るのが適当である。In this case, a polar rubber such as styrene-butadiene rubber, epichlorohydrin rubber, acrylic rubber, or chloroprene rubber, or a high-resistance rubber such as silicone rubber, EPDM, or fluororubber, in which low-resistance particles such as carbon are dispersed, is used. Particularly preferred is silicone rubber, which can be made to have a low grade without using a plasticizer or the like. These materials can be obtained by ordinary molding means such as press molding, injection molding, extrusion molding, etc., and can be further formed into a predetermined shape by polishing. The thickness of this conductive elastic layer is suitably 1 mm or more in order to exhibit a sufficient elastic effect.
樹脂層21はアルキッド樹脂、塩素化ポリエーテル、塩
素化ポリエチレン、エポキシ樹脂、フッ素樹脂、フェノ
ール樹脂、ポリアミド、ポリカーボネート、ポリエチレ
ン、メタクリル樹脂、ポリプロピレン、ポリスチレン、
ポリウレタン、ポリ塩化ビニル、ポリ塩化ビニリデン、
シリコーン等の樹脂、ブタジェンゴム、スチレンブタジ
ェンゴム、エチレンプロピレンゴム、クロロブレンゴム
、塩素化ポリエチレン、エピクロルヒドリンゴム、ニト
リルゴム、アクリルゴム、シリコーンゴム、フッ素ゴム
等のゴムから形成されるが、耐熱性、耐湿性の観点から
みてシリコーン樹脂、フッ素系樹脂の使用が好ましい。The resin layer 21 is made of alkyd resin, chlorinated polyether, chlorinated polyethylene, epoxy resin, fluororesin, phenol resin, polyamide, polycarbonate, polyethylene, methacrylic resin, polypropylene, polystyrene,
polyurethane, polyvinyl chloride, polyvinylidene chloride,
It is formed from resins such as silicone, rubbers such as butadiene rubber, styrene-butadiene rubber, ethylene propylene rubber, chlorobrene rubber, chlorinated polyethylene, epichlorohydrin rubber, nitrile rubber, acrylic rubber, silicone rubber, fluorine rubber, etc., but has heat resistance, From the viewpoint of moisture resistance, it is preferable to use silicone resins and fluororesins.
この樹脂層21の膜厚は体積抵抗や誘電率等の電気特性
を考慮することにより任意に定め得るが、通常50μ厘
〜2asである。この層を作成するにはスプレー塗布、
ディッピング、水蒸気加硫、押出加硫等の適切な工法を
適宜採用すれば良い。The thickness of this resin layer 21 can be arbitrarily determined by considering electrical properties such as volume resistance and dielectric constant, but is usually 50 μm to 2 as. To create this layer, spray application,
An appropriate method such as dipping, steam vulcanization, or extrusion vulcanization may be employed as appropriate.
本発明はこの層に界面活性剤を混入させることにより達
成されるが、この界面活性剤はノニオン性、カチオン性
、アニオン性、両性いずれのものも使用できる。具体的
には、ノニオン性のものとしては、脂肪酸などのエステ
ル化合物、エーテルエステル化合物、エーテル化合物、
アミド縮合物などが挙げられ、カチオン性のものとして
は、脂肪族アミン塩及びその4級アンモニウム塩、芳香
族四級アンモニウム塩、複素環4級アンモニウム塩等、
アニオン性のものとしては、アルキルカルボン酸塩、N
−アシルアミノ酸塩、アルキルエーテルカルボン酸塩、
アシル化ペプチド、アルキルスルホン酸塩、アルキルベ
ンゼン及びアルキルナフタレンスルホン酸塩、フルホコ
ハク酸塩、α−オレフィンスルホン酸塩、N−アシルス
ルホン酸塩、アルキル硫酸塩、アルキルエーテル硫酸塩
、アルキルアリルエーテル硫酸塩、アルキルアミド硫酸
塩、アルキルリン酸塩、アルキルエーテルリン酸塩、ア
ルキルアリルエーテルリン酸塩等、両性のものとしては
カルボキシベタイン、スルホベタイン、アミノカルボン
酸塩等があげられる。The present invention is achieved by incorporating a surfactant into this layer, and any of nonionic, cationic, anionic, and amphoteric surfactants can be used. Specifically, nonionic compounds include ester compounds such as fatty acids, ether ester compounds, ether compounds,
Amide condensates, etc., and cationic ones include aliphatic amine salts and their quaternary ammonium salts, aromatic quaternary ammonium salts, heterocyclic quaternary ammonium salts, etc.
Anionic ones include alkyl carboxylates, N
-acyl amino acid salt, alkyl ether carboxylate,
Acylated peptides, alkyl sulfonates, alkylbenzene and alkylnaphthalene sulfonates, fluphosuccinates, α-olefin sulfonates, N-acylsulfonates, alkyl sulfates, alkyl ether sulfates, alkyl allyl ether sulfates, Alkylamide sulfates, alkyl phosphates, alkyl ether phosphates, alkyl allyl ether phosphates, etc., and amphoteric ones include carboxybetaine, sulfobetaine, aminocarboxylate, and the like.
本発明において、上記界面活性剤として、特にフッ素系
の界面活性剤を含有させる場合には、耐環境性が優れて
おり、好ましい。このフッ素系界面活性剤はノニオン性
、カチオン性、アニオン性、両性のいずれも使用可能で
あり、具体的には以下のものがある。In the present invention, it is preferable to include a fluorine-based surfactant as the above-mentioned surfactant because it has excellent environmental resistance. Any of nonionic, cationic, anionic, and amphoteric fluorine-based surfactants can be used, and specific examples include the following.
ノニオン性のものとしては、パーフルオロアルキル基親
油性基含有オリゴマー、パーフルオロアルキル基親水性
基含有オリゴマー、パーフルオロアルキルエチレンオキ
シド付加物などが挙げられ、カチオン性のものとしては
、パーフルオロアルキル含有jfliJ級アンモニウム
塩など、アニオン性のものとしてはパーフルオロアルキ
ルを含有したスルホン酸、カルボン酸の一価金属塩やリ
ン酸エステルなど、
両性のものとしてはパーフルオロアルキルを含有したベ
タインなどが挙げられる。Nonionic ones include perfluoroalkyl lipophilic group-containing oligomers, perfluoroalkyl hydrophilic group-containing oligomers, perfluoroalkyl ethylene oxide adducts, and cationic ones include perfluoroalkyl-containing jfliJ. Examples of anionic compounds such as ammonium salts include perfluoroalkyl-containing sulfonic acids, monovalent metal salts of carboxylic acids and phosphoric acid esters, and amphoteric compounds include perfluoroalkyl-containing betaines.
これらは用いる樹脂又はゴムとの相溶性等の点から適宜
選択することができる。又、ノニオン性界面活性剤との
混合併用も可能である。These can be appropriately selected from the viewpoint of compatibility with the resin or rubber used. Further, it is also possible to use them in combination with a nonionic surfactant.
この界面活性剤の混入量はバインダー樹脂の固形分10
0重量部に対して、0.1〜50重量部が好ましい。よ
り好ましくは0,5〜20重量部であ゛る。0.1重量
部以下であると効果が充分現れずに残像が発生する。逆
に50重量部を超えると耐摩耗性、耐環境性の劣化、ト
ナー搬送性の低下などが生じる。The amount of this surfactant mixed is 10% of the solid content of the binder resin.
It is preferably 0.1 to 50 parts by weight relative to 0 parts by weight. More preferably, it is 0.5 to 20 parts by weight. If the amount is less than 0.1 part by weight, the effect will not be sufficiently exhibited and an afterimage will occur. On the other hand, if it exceeds 50 parts by weight, abrasion resistance, environmental resistance, and toner transportability may deteriorate.
又、本発明で用いる現像ローラには種々の目的の為に無
機充填剤や架橋剤、熱安定剤、加工助剤などを添加する
ことができる。無機充填剤としては、珪藻土、石英粉末
、酸化鉄、酸化亜鉛、酸化チタン、酸化カルシウム、酸
化マグネシウム、タルク、珪酸アルミニウム、酸化アル
ミニウムなどの粉末、チタン酸カリウム、アスベスト、
ガラス、カーボンなどの繊維、テフロン、窒化ホウ素な
どの粉末が用いられる。Furthermore, inorganic fillers, crosslinking agents, heat stabilizers, processing aids, etc. can be added to the developing roller used in the present invention for various purposes. Inorganic fillers include diatomaceous earth, quartz powder, iron oxide, zinc oxide, titanium oxide, calcium oxide, magnesium oxide, talc, aluminum silicate, aluminum oxide powder, potassium titanate, asbestos,
Fibers such as glass and carbon, and powders such as Teflon and boron nitride are used.
又、トナーとしては、正帯電性、負帯電性のどちらでも
良く、従来公知のものが使用できる。Further, the toner may be either positively chargeable or negatively chargeable, and conventionally known toners can be used.
このようなトナーの具体例としては、例えばスチレン−
n−ブチルメタクリレートやエポキシ樹脂などの結着樹
脂中に着色剤を含有させた微粒体や更に必要に応じて帯
電制御剤にグロシン染料、塩基性染料など)、シリカな
どの流動化剤、炭化ケイ素などの研磨剤、脂肪酸金属塩
などの潤滑剤などを添加したもの等が挙げられる。Specific examples of such toner include, for example, styrene-
Fine particles containing a coloring agent in a binder resin such as n-butyl methacrylate or epoxy resin, and if necessary, a charge control agent such as glosine dye or basic dye), a fluidizing agent such as silica, and silicon carbide. Examples include those to which abrasives such as, lubricants such as fatty acid metal salts, etc. are added.
[実施例]
以下、実施例及び比較例により本発明を更に詳細に説明
する。[Examples] Hereinafter, the present invention will be explained in more detail with reference to Examples and Comparative Examples.
実施例1
予め導電ブライマー(トーレシリコーン社製:DY39
−O1l)が塗布された芯金(Biiφ)上に下記の導
電性弾性層形成成分を1次加流:170℃/10分、1
20kg/cm2、二次川流: 200℃74時間の
条件下でプレス成形し肉厚6m閣の導電性弾性層(体積
固有抵抗: 1.5X 105Ω・C−、ゴム硬度(
JIS^):28度)を形成した。Example 1 Conductive brimer (manufactured by Toray Silicone Co., Ltd.: DY39)
-O1l) was coated with the following conductive elastic layer forming components on the core metal (Biiφ): 170°C/10 minutes, 1
20kg/cm2, secondary flow rate: 6m thick conductive elastic layer press-molded under conditions of 200°C for 74 hours (volume resistivity: 1.5X 105Ω・C-, rubber hardness (
JIS^): 28 degrees) was formed.
[導電性弾性層形成成分]
メチルビニルポリシロキサン 100重量部カーボン(
ケッチエンブラックEC)
5重量部
石英 20重量部上記混合物を
2本ロールで混練した後、混合物100重量部に対し架
橋剤(2,4−ジメチル−2゜4−ジ−ターシャリープ
チルパーオキシヘキサン:トーレシリコーン社製: R
C−4) 1.5重量部を添加したもの。[Conductive elastic layer forming component] Methyl vinyl polysiloxane 100 parts by weight carbon (
Ketchen Black EC) 5 parts by weight Quartz 20 parts by weight The above mixture was kneaded with two rolls, and then a crosslinking agent (2,4-dimethyl-2°4-di-tert-butylperoxyhexane) was added to 100 parts by weight of the mixture. : Manufactured by Toray Silicone Co., Ltd.: R
C-4) Added 1.5 parts by weight.
次いで、導電性弾性層表面をトリクレンにより洗浄した
後、チタネート系カップリング剤(松本製薬社製: T
A−25)の圭%キシレン溶液を塗布し、30分間乾燥
後、下記の樹脂層形成成分をスプレーコーティングし、
150℃/1時間の条件で硬化させ、ついで研磨して膜
厚50μ厘の樹脂層を形威し、現像ローラを作成した。Next, after cleaning the surface of the conductive elastic layer with trichlene, a titanate coupling agent (manufactured by Matsumoto Pharmaceutical Co., Ltd.: T
A-25) Kei% xylene solution was applied, and after drying for 30 minutes, the following resin layer forming components were spray coated,
The resin was cured at 150° C. for 1 hour, and then polished to form a resin layer with a thickness of 50 μm, thereby producing a developing roller.
[樹脂層形成成分]
フッ素系共重合体樹脂(固形分50%)(旭硝子■社製
二ルミフロン801C)100重量部
コロネートEH(50%キシレン溶液)20重量部
M E K 400重量部フッ
素系カチオン性界面活性剤
(CI FI7S02 NH(C3H! )N” (
CH3) 31− )5重量部
実施fFlj 2
実施例1で用いるフッ素系カチオン性界面活性剤に代り
にフッ素系アニオン性界面活性剤(C7F Is C0
0Na)を用いる他は、実施例1と同じとした。[Resin layer forming components] Fluorine copolymer resin (solid content 50%) (Nilumiflon 801C manufactured by Asahi Glass Company) 100 parts by weight Coronate EH (50% xylene solution) 20 parts by weight M E K 400 parts by weight fluorine cation surfactant (CI FI7S02 NH (C3H!)N” (
CH3) 31-) 5 parts by weight fFlj 2 In place of the fluorine-based cationic surfactant used in Example 1, a fluorine-based anionic surfactant (C7F Is C0
The procedure was the same as in Example 1 except that 0Na) was used.
実施例3
実施例1で用いるフッ素系カチオン性界面活性剤のかわ
りに、フッ素系両性界面活性剤[CI F17SO2N
H(C2H4)N” (CH3) 2tC2H+(0
0″″〕を用いる他は実施例1と同じとした。Example 3 Instead of the fluorine-based cationic surfactant used in Example 1, a fluorine-based amphoteric surfactant [CI F17SO2N
H(C2H4)N” (CH3) 2tC2H+(0
The procedure was the same as in Example 1 except that 0″″] was used.
実施例4
実施f!II 1におけるフッ素系カチオン性界面活性
剤の代わりに炭化水素系カチオン性界面活性剤[Cl2
HzsSO2NH(C3Hs )N” (CH3)
3 I −1を用いる他は同じとした。Example 4 Implementation f! In place of the fluorine-based cationic surfactant in II 1, a hydrocarbon-based cationic surfactant [Cl2
HzsSO2NH(C3Hs)N” (CH3)
The procedure was the same except that 3 I-1 was used.
実施例5
実施例1におけるフッ素系界面活性剤のかわりに炭化水
素系アニオン性界面活性剤(Cy Hl5COONa)
を用いる他は同じとした。Example 5 A hydrocarbon-based anionic surfactant (Cy Hl5COONa) was used instead of the fluorine-based surfactant in Example 1.
The same procedure was used except that .
実施例6
実施例1におけるフッ素系界面活性剤のかわりに炭化水
素系両性界面活性剤(C14H2,CHOO−)を用い
る他は同じとした。、N(CH3)比較例1
実施例1における界面活性剤を使用しない他は同じとし
た。Example 6 The same procedure as in Example 1 was carried out except that a hydrocarbon-based amphoteric surfactant (C14H2, CHOO-) was used instead of the fluorine-based surfactant. , N(CH3) Comparative Example 1 The same procedure as in Example 1 was used except that the surfactant was not used.
比較例2
実施例1における界面活性剤の代わりに以下のちのを用
いる他は同じとした。Comparative Example 2 The same procedure was used as in Example 1 except that the following was used instead of the surfactant.
カーボンブラックマスターバッチ
15重量部
なお、カーボンマスターバッチは以下のようにして調製
した。Carbon black masterbatch 15 parts by weight The carbon masterbatch was prepared as follows.
フッ素系共重合体樹脂(固形分50%)(旭硝子■社製
:ルミフロン801C)100重量部
カーボンブラック(ブラックバー
ルL:キャボット社製)40重量部
トルエン 50重量部キシレン
50重量部上記混合物を72時間ボー
ルミルで分散してカーボンマスターバッチを調製した。Fluorine copolymer resin (solid content 50%) (manufactured by Asahi Glass Company: Lumiflon 801C) 100 parts by weight Carbon black (Black Bar L: manufactured by Cabot Corporation) 40 parts by weight Toluene 50 parts by weight Xylene
A carbon masterbatch was prepared by dispersing 50 parts by weight of the above mixture in a ball mill for 72 hours.
比較例3
比較例2におけるカーボンブラックマスターバッチを1
5重量部から50重量部とする他は同じとした。Comparative Example 3 The carbon black masterbatch in Comparative Example 2 was
The same procedure was used except that the amount was changed from 5 parts by weight to 50 parts by weight.
以上のようにして得られた実施例及び比較例の現像ロー
ラを各々第1図における現像ローラとして用い、トナー
の帯電量、トナーの離型性、現像ローラ摩耗性、残像性
及び画像ムラの各項目についてそれぞれ、10℃24%
、22℃50%、30”080%の各環境下において評
価した。その結果を表−1に示す。評価方法は以下によ
った。The developing rollers of Examples and Comparative Examples obtained as described above were used as the developing rollers shown in FIG. 10℃24% for each item
, 22° C. 50%, and 30”080%. The results are shown in Table 1. The evaluation method was as follows.
[トナーの帯電量]
下記の付帯型トナーを用い第1図に示す現像装置におい
ての帯電量をブローオフ法により測定した。[Charge amount of toner] The charge amount in the developing device shown in FIG. 1 was measured by the blow-off method using the accompanying type toner described below.
(使用トナー)二粒径12!r−■
スチレンアクリル樹脂 100重量部カーボン
10重量部含クロムモノアゾ染料
2重量部〔トナーの離型性〕
上記のトナー及び現像装置を用いて、72時間空回した
後の現像ローラ表面のトナー状態を次の基準により評価
した。(Toner used) Two particle size 12! r-■ Styrene acrylic resin 100 parts by weight carbon
10 parts by weight chromium-containing monoazo dye
2 parts by weight [Toner releasability] Using the above toner and developing device, the state of the toner on the surface of the developing roller after running idly for 72 hours was evaluated according to the following criteria.
ランクA:布などでローラ表面のトナーが簡単にふきと
れる。Rank A: Toner on the roller surface can be easily wiped off with a cloth.
ランクB:ふきとりで、わずかにトナーが残る。Rank B: A slight amount of toner remains after wiping.
ランクC:完全にふきとりができずトナーの薄膜が残る
。Rank C: The toner cannot be completely wiped off and a thin film of toner remains.
ランクD=溶融状態のトナーが強くローラ表面に固着し
ている。Rank D=Toner in a molten state is strongly adhered to the roller surface.
上記と同様のトナー及び現像装置を用いて、20時間空
回し後の摩耗量を現像ローラの直径を測ることによって
測定した。なお、ローラの直径はレーザーマイクロゲー
ジ(DT−4002A ;岩通エレクトロニクス)によ
り測定した。Using the same toner and developing device as above, the amount of wear after running idle for 20 hours was measured by measuring the diameter of the developing roller. The diameter of the roller was measured using a laser micro gauge (DT-4002A; Iwatsu Electronics).
[残像性の評価]
上記と同様のトナー及び現像装置を用いパターン画像に
より残像を評価した。即ち、黒ベタ現像後、網点を現像
し、黒ベタの位置に相当する網点の画像濃度(IDL)
と黒ベタ相当部以外の、その真横部の網点画像濃度(I
Do)との比(r D L / r D H)をマクベ
ス濃度計により測定した。なお左右2ケ所においてその
比を測定した。[Evaluation of afterimage property] Afterimage was evaluated based on a pattern image using the same toner and developing device as above. That is, after solid black development, halftone dots are developed, and the image density (IDL) of the halftone dots corresponding to the position of the black solid is determined.
and the halftone image density (I
Do) and the ratio (r DL / r DH) was measured using a Macbeth densitometer. The ratio was measured at two locations on the left and right.
[画像ムラの評価]
黒ベタの現像ローラ1回転分中の1点をとり、更に5回
転分までの計5点について、マクベス濃度計で各々のI
Dを測定し、ID10DX 100の鎧を求めた。[Evaluation of image unevenness] Take one point during one rotation of the black solid developing roller, and then measure each I with a Macbeth densitometer for a total of 5 points for up to 5 rotations.
Measured D and found armor with ID10DX100.
OD:黒ベタ部原稿濃度
ID:黒ベタ部の複写濃度
なお、トナー薄層ブレード、補給ローラ及び感光体とし
ては以下のものを用いた。OD: Original density of solid black portion ID: Copy density of solid black portion Note that the following were used as the toner thin layer blade, replenishment roller, and photoreceptor.
[トナー薄層ブレードゴ
シリコーンゴム(II1m厚)
[トナー補給ローラ]
導電性ウレタンスポンジ
[感光体]
P C
[発明の効果]
以上説明したように、本発明によりイオン性界面活性剤
を含有する樹脂層をトナー担持体上に設けたことにより
、残像を防止することができ、又、同時にトナー帯電量
、トナー離型性、トナー担持体の耐摩性にも良好な結果
を与える。[Toner thin layer blade silicone rubber (II 1m thick) [Toner replenishment roller] Conductive urethane sponge [Photoreceptor] P C [Effects of the invention] As explained above, the resin containing an ionic surfactant according to the present invention By providing the layer on the toner carrier, it is possible to prevent afterimages, and at the same time, good results are obtained in terms of toner charge amount, toner releasability, and abrasion resistance of the toner carrier.
第1図は本発明の現像装置を示す概略図、第2図は本発
明に用いるトナー担持体の構成を説明する図。FIG. 1 is a schematic diagram showing a developing device of the present invention, and FIG. 2 is a diagram illustrating the structure of a toner carrier used in the present invention.
Claims (3)
該保持体に潜像を顕像化せしめるトナー担持体、及び該
トナー担持体上にトナーの薄層を形成せしめる規制部材
からなる現像装置において、前記トナー担持体に界面活
性剤を含有する樹脂層を設けたことを特徴とする現像装
置。(1) An electrostatic latent image holder that holds at least an electrostatic latent image;
In a developing device comprising a toner carrier for making a latent image visible on the holder, and a regulating member for forming a thin layer of toner on the toner carrier, a resin layer containing a surfactant on the toner carrier. A developing device characterized by being provided with.
項(1)に記載の現像装置。(2) The developing device according to claim (1), wherein the surfactant is an ionic surfactant.
である請求項(1)又は(2)に記載の現像装置。(3) The developing device according to claim 1 or 2, wherein the surfactant is a fluorine-based ionic surfactant.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1266321A JP3065323B2 (en) | 1989-10-16 | 1989-10-16 | Developing device |
US07/596,464 US5168312A (en) | 1989-10-16 | 1990-10-12 | Unit for developing electrostatic latent images including member having overcoat layer |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1266321A JP3065323B2 (en) | 1989-10-16 | 1989-10-16 | Developing device |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH03129368A true JPH03129368A (en) | 1991-06-03 |
JP3065323B2 JP3065323B2 (en) | 2000-07-17 |
Family
ID=17429300
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1266321A Expired - Fee Related JP3065323B2 (en) | 1989-10-16 | 1989-10-16 | Developing device |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3065323B2 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101733886B (en) * | 2008-11-13 | 2012-07-25 | 明安国际企业股份有限公司 | Method for manufacturing composite workpiece with barbs |
-
1989
- 1989-10-16 JP JP1266321A patent/JP3065323B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JP3065323B2 (en) | 2000-07-17 |
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