JPH03168664A - Developing device - Google Patents
Developing deviceInfo
- Publication number
- JPH03168664A JPH03168664A JP1307507A JP30750789A JPH03168664A JP H03168664 A JPH03168664 A JP H03168664A JP 1307507 A JP1307507 A JP 1307507A JP 30750789 A JP30750789 A JP 30750789A JP H03168664 A JPH03168664 A JP H03168664A
- Authority
- JP
- Japan
- Prior art keywords
- toner
- resin
- surfactant
- conductive
- long period
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 229920005989 resin Polymers 0.000 claims abstract description 45
- 239000011347 resin Substances 0.000 claims abstract description 45
- 239000004094 surface-active agent Substances 0.000 claims abstract description 15
- 239000000758 substrate Substances 0.000 claims abstract description 13
- 230000001105 regulatory effect Effects 0.000 claims description 15
- 239000011737 fluorine Substances 0.000 claims description 9
- 229910052731 fluorine Inorganic materials 0.000 claims description 9
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 239000010410 layer Substances 0.000 abstract description 37
- 239000000463 material Substances 0.000 abstract description 5
- 239000011247 coating layer Substances 0.000 abstract description 2
- -1 fluororesin Substances 0.000 description 15
- 229910052751 metal Inorganic materials 0.000 description 14
- 239000002184 metal Substances 0.000 description 14
- 238000000034 method Methods 0.000 description 13
- 239000002563 ionic surfactant Substances 0.000 description 9
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 8
- 229920001971 elastomer Polymers 0.000 description 7
- 239000005060 rubber Substances 0.000 description 7
- 150000002739 metals Chemical class 0.000 description 6
- 125000005010 perfluoroalkyl group Chemical group 0.000 description 6
- 108091008695 photoreceptors Proteins 0.000 description 6
- 125000000129 anionic group Chemical group 0.000 description 5
- 125000002091 cationic group Chemical group 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 230000007774 longterm Effects 0.000 description 4
- 229920002379 silicone rubber Polymers 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- KWIUHFFTVRNATP-UHFFFAOYSA-O N,N,N-trimethylglycinium Chemical compound C[N+](C)(C)CC(O)=O KWIUHFFTVRNATP-UHFFFAOYSA-O 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
- 239000002280 amphoteric surfactant Substances 0.000 description 3
- 229960003237 betaine Drugs 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 229920006026 co-polymeric resin Polymers 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- 238000007598 dipping method Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000007613 environmental effect Effects 0.000 description 3
- 230000004927 fusion Effects 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 235000021317 phosphate Nutrition 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 229920002050 silicone resin Polymers 0.000 description 3
- 239000004945 silicone rubber Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000008096 xylene Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-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
- 229920000459 Nitrile rubber Polymers 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000010408 film Substances 0.000 description 2
- 229920001973 fluoroelastomer Polymers 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 2
- 150000003871 sulfonates Chemical class 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
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 241000238557 Decapoda Species 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
- 239000004952 Polyamide 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
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- 229920006311 Urethane elastomer Polymers 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000003082 abrasive agent Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229920000800 acrylic rubber Polymers 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
- 125000005192 alkyl ethylene 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
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000000981 basic dye Substances 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- DFYKHEXCUQCPEB-UHFFFAOYSA-N butyl 2-methylprop-2-enoate;styrene Chemical compound C=CC1=CC=CC=C1.CCCCOC(=O)C(C)=C DFYKHEXCUQCPEB-UHFFFAOYSA-N 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- XENVCRGQTABGKY-ZHACJKMWSA-N chlorohydrin Chemical compound CC#CC#CC#CC#C\C=C\C(Cl)CO XENVCRGQTABGKY-ZHACJKMWSA-N 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical class OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000002923 metal particle 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
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 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
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920005990 polystyrene resin 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
- 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
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 229920005792 styrene-acrylic resin Polymers 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
- 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]
本発明は、一或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 [Industrial Field of Application] The present invention relates to an electrostatic latent image developing device using a monochromatic toner.
[従来の技術]
従来、非磁性一或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(すなわち現像ローラ)上のト
ナーをブレード状あるいはロール状の部材(トナー規制
部材)により薄層化し、これを静電潜像の形成された感
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、トナーはトナー規制部材によって薄層とな
る時にこのトナー規制部材及び現像ローラとの摩擦によ
って帯電させられる。このブレード状あるいはロール状
のトナー規制部材は例えば金属製のものを用いるものが
あるが、金属では摩擦帯電によってトナーに充分なる帯
電量を与えることができない。[Prior Art] Conventionally, as a method for developing an electrostatic latent image using non-magnetic toner, the toner on a toner carrier (i.e., a developing roller) is controlled by a blade-shaped or roll-shaped member (toner regulating member). A method is known in which the electrostatic latent image is formed into a thin layer and brought into contact with a photoreceptor on which an electrostatic latent image has been formed to develop it. In this method, when the toner is formed into a thin layer by the toner regulating member, it is charged by friction between the toner regulating member and the developing roller. This blade-shaped or roll-shaped toner regulating member is sometimes made of metal, but metal cannot provide a sufficient amount of charge to the toner due to frictional charging.
そこで、この金属製の部材にバイアスを印加し、トナー
に電荷を付与する電荷注入の方法がある。これによって
トナーに与える帯電を制御することが可能となる。しか
し、金属製のトナー薄層化部材はトナーとの離型性が悪
いために、トナーがこの部材の表面に固着してしまい、
長期安定した帯電付与や均一薄層化ができなくなる。Therefore, there is a charge injection method in which a bias is applied to this metal member to impart charge to the toner. This makes it possible to control the charge applied to the toner. However, since the metal toner thinning member has poor releasability from the toner, the toner adheres to the surface of the member.
It becomes impossible to provide long-term stable charging and uniform thinning of the layer.
この問題に対し特願昭 号にみられるように、
トナー規制部材に離型性に優れたボリマーやフッ素樹脂
等を使用する事が提案されている。これによってトナー
の固着が防止され、又同時に充分な帯電量も付与できる
。In response to this problem, as seen in Tokugan Sho issue,
It has been proposed to use polymers, fluororesins, etc. with excellent mold releasability as the toner regulating member. This prevents the toner from sticking and at the same time provides a sufficient amount of charge.
しかし、これ等のボリマーは絶縁性の樹脂であるために
、トナーとの帯電時にトナー規制部材中に発生する逆極
性の帯電電荷が残留しやすく、その残留電荷が以下の様
な影響を及ぼす。However, since these polymers are insulating resins, charges of opposite polarity generated in the toner regulating member when charged with toner tend to remain, and the remaining charges have the following effects.
■ トナーが飽和帯mffiまでに達する時間(トナー
の帯電の立ち上がり性)が遅くなる。(2) The time it takes for the toner to reach the saturation band mffi (the rise in charging of the toner) is delayed.
■ 長期連続運転を行うと、トナーの飽和帯電量が次第
に低下する。■ After long-term continuous operation, the saturation charge amount of the toner gradually decreases.
従って長期安定した良品質の画像を得るには至らない。Therefore, it is not possible to obtain images of good quality that are stable over a long period of time.
この問題を解決するために、ボリマー中にカーボン等の
低抵抗粒子を混入し、体積抵抗を低下させ残留電荷をリ
ークしやすくする試みがなされたが、離型性が低下し、
トナー融着が発生する等の不都合が生じ、他の対策が求
められていた。In order to solve this problem, attempts were made to mix low-resistance particles such as carbon into the polymerer to lower the volume resistance and make it easier to leak residual charge, but this resulted in poor mold releasability and
Problems such as toner fusion occur, and other countermeasures have been required.
[発明が解決しようとする課題コ
本発明はこうした実情に鑑み、トナーへの帯電性に優れ
ると共に、トナー融着を発生することがなく、かつ、こ
れらの特性を長期安定して持続することができるトナー
規制部材を備えた現像装置を提供することを目的とする
ものである。[Problems to be Solved by the Invention] In view of these circumstances, the present invention has been developed to provide a method that has excellent toner charging properties, does not cause toner fusion, and can maintain these characteristics stably for a long period of time. It is an object of the present invention to provide a developing device equipped with a toner regulating member that can be used.
[課題を解決するための千段]
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、トナー規制部材を、導電性基体に界面活性剤を
含有する樹脂被覆層を形成した横成とすることが有効で
あることを見出し、発明に至った。[A Thousand Steps to Solve the Problems] As a result of intensive studies to solve the above-mentioned problems, the present inventors developed a toner regulating member by forming a horizontal conductive substrate with a resin coating layer containing a surfactant. They discovered that it is effective to make the structure of the invention, and came up with the invention.
すなわち、本発明は少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、前記規制部材は
導電性基体上にイオン性界面活性剤を含有する樹脂層を
具備している現像装置である。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. In a developing device including a regulating member, the regulating member includes a resin layer containing an ionic surfactant on a conductive substrate.
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lは容器、2はトナー 3はアジテー
タ4は補給ローラ、5はトナー担持体としての現像ロー
ラ、6はトナー規制部材としてのトナー薄層ブレード、
7は静電潜像保持体としての感光体である。In FIG. 1, l is a container, 2 is a toner, 3 is an agitator 4 is a supply roller, 5 is a developing roller as a toner carrier, 6 is a toner thin layer blade as a toner regulating member,
7 is a photoreceptor as an electrostatic latent image holder.
第1図において、トナー容器1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と現像ローラ 5により形成され
るトナー貯蔵部に搬送され、現像ローラ 5の表面に担
持される。更にトナー薄層ブレード6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。In FIG. 1, a toner container 1 contains a non-magnetic monocomponent toner 2. As shown in FIG. This toner 2 is conveyed by an agitator 3 to a toner storage section formed by a supply roller 4 and a developing roller 5, and is carried on the surface of the developing roller 5. Furthermore, a uniform thin layer is formed by the toner thin layer blade 6, and the toner is triboelectrically charged to a predetermined polarity.
トナー薄層は静電潜像を保持する感光体7と現像ローラ
5とが当接する現像領域に運ばれ、ここで現像ローラか
ら感光体7ヘトナーが静電的に移行し、潜像が顕像化さ
れる。The thin layer of toner is transported to the development area where the photoreceptor 7 holding the electrostatic latent image and the developing roller 5 come into contact, where the toner is electrostatically transferred from the developing roller to the photoreceptor 7 and the latent image is developed. be converted into
又、第2図においてはトナー規制部材として、ロール状
のものを用いた場合で、このトナー薄層ローラは現像ロ
ーラとの当接領域において、現像ローラと逆向きに回転
する。Further, FIG. 2 shows a case where a roll-shaped member is used as the toner regulating member, and this toner thin layer roller rotates in the opposite direction to the developing roller in the area where it contacts the developing roller.
以上のプロセスにおいて、薄層ブレード、あるいは薄層
ローラなどの手段によってトナーを均一薄層とするとと
もに所定の極性に帯電させるわけだが、均一薄層とする
ために、これら規制部材によりトナーに大きな当接圧が
かかつている。In the above process, the toner is made into a uniform thin layer by means such as a thin layer blade or a thin layer roller, and is charged to a predetermined polarity. Contact pressure is applied.
このため、既に述べたように長期使用すると、これら薄
層部材にトナーが融着してしまい薄層の乱れ、帯電量の
低下などを生じる。Therefore, as described above, when used for a long period of time, toner is fused to these thin layer members, resulting in disturbance of the thin layer and a decrease in the amount of charge.
本発明ではこのようなトナー融着をしない、かつ対トナ
ー帯電性の優れた材料を、トナー規制部材に用い、更に
対トナー帯電性の長期安定性を得るために、前述の特定
構造とする。In the present invention, a material that does not cause such toner fusion and has excellent toner charging properties is used for the toner regulating member, and furthermore, in order to obtain long-term stability in toner charging properties, the above-mentioned specific structure is provided.
第3図a1第4図aにトナー規制部材の例を示す。第3
図aはブレード状、第4図aはロール状のものであり、
金属等の導電性基体3{、41上に界面活性剤32、4
2を含む樹脂層32、42をコーティングした構或のも
のである。Examples of the toner regulating member are shown in FIG. 3a and FIG. 4a. Third
Figure a shows a blade shape, Figure 4 a shows a roll shape,
Surfactants 32, 4 on conductive substrates 3 {, 41 such as metals
The structure is coated with resin layers 32 and 42 containing 2.
又、第3図a、第4図aの変形例として界面活性剤33
−、43−を含有する樹脂層32−、42−」二に更に
樹脂層34−、44=を設けた第3図b1第4図bに示
すような構成としてもよい。In addition, as a modification of FIGS. 3a and 4a, surfactant 33
3b and 4b, in which resin layers 32- and 42- containing resin layers 32- and 43- are further provided with resin layers 34- and 44=.
上述したとおり樹脂には帯電電荷が蓄積する。As described above, electrical charges are accumulated in the resin.
しかし、界面活性剤を混入した樹脂層を導電性基体上に
設けることによりこの導電性基体と樹脂との間の電荷移
動性が向上するために、樹脂の帯電電荷と逆極性の電荷
が、アースより導電性基体、樹脂層へと円滑に注入され
樹脂の摩擦帯電能力を初期化できるためである。However, by providing a resin layer mixed with a surfactant on the conductive substrate, the charge mobility between the conductive substrate and the resin is improved, so that the charge with the opposite polarity to the charge on the resin is transferred to the ground. This is because it is more smoothly injected into the conductive substrate and resin layer, and the triboelectric charging ability of the resin can be initialized.
導電性基体31、31− 、41, 41−は金属や導
電性を付与した樹脂又はゴムなどで形成される。The conductive substrates 31, 31-, 41, 41- are formed of metal, conductive resin, rubber, or the like.
金属には従来公知の例えばステンレス、鉄、銅、アルミ
ニウムなどが用いられる。Conventionally known metals such as stainless steel, iron, copper, and aluminum are used as the metal.
導電性の樹脂又はゴムはカーボンブラック、金属粒子な
どの導電性粒子を混入することによって導電性を付与す
る。Conductive resin or rubber is imparted with conductivity by mixing conductive particles such as carbon black or metal particles.
本発明に用いる樹脂、ゴムしては、樹脂としては、例え
ばアルキッド樹脂、塩素化ポリエーテル、塩素化ポリエ
チレン、エボキシ樹脂、フッ素樹脂、フェノール樹脂、
ボリアミド、ポリカーボネート、ポリエチレン、メタク
リル樹脂、ボリブロビレン、ボリスチレン系樹脂、ポリ
ウレタン、ポリ塩化ビニル、ポリ塩化ビニリデン、シリ
コーン等の樹脂類が、又ゴムとしてはブタジエンゴム(
BR) スチレンブタジエンゴム(SBR) 、エ
チレン・プロピレンゴム(CR) 、塩素化ポリエチレ
ン、エビクロルヒドリンゴム(CUR) 、ニトリルゴ
ム(NBR) 、アクリルゴム、ウレタンゴム、シリコ
ーンゴム、フッ素ゴム等のゴム類が挙げられるが、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、シリコーンゴム、フッ素ゴムが好ましい。Examples of the resin and rubber used in the present invention include alkyd resin, chlorinated polyether, chlorinated polyethylene, epoxy resin, fluororesin, phenol resin,
Resins such as polyamide, polycarbonate, polyethylene, methacrylic resin, polypropylene, polystyrene resin, polyurethane, polyvinyl chloride, polyvinylidene chloride, silicone, and butadiene rubber (
BR) Rubbers such as styrene-butadiene rubber (SBR), ethylene-propylene rubber (CR), chlorinated polyethylene, shrimp chlorohydrin rubber (CUR), nitrile rubber (NBR), acrylic rubber, urethane rubber, silicone rubber, fluororubber, etc. From the viewpoint of heat resistance and moisture resistance, silicone resins, fluororesins, silicone rubbers, and fluororubbers are preferred.
この導電性基体の上にコートする樹脂層には上記と同様
の樹脂又はゴムを使用することができる。本発明ではこ
の層の中に界面活性剤を含有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、両性のいずれのものも使用できる。The same resin or rubber as above can be used for the resin layer coated on this conductive substrate. In the present invention, this is achieved by incorporating a surfactant into this layer, and any of nonionic, cationic, anionic, and amphoteric surfactants can be used.
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る。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4級アンモニウム塩、複素環4級アンモニウム
塩等を挙げることができる。Specifically, nonionic compounds include ester compounds such as fatty acids, ether ester compounds, ether compounds, and amide condensates. Examples of cationic salts include aliphatic amine salts and their quaternary ammonium salts, aromatic quaternary ammonium salts, and heterocyclic quaternary ammonium salts.
アニオン性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
ベプチド、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、スルホコハク酸塩
、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を挙げることができる。Anionic salts include alkyl carboxylates, N-acylamino acid salts, alkyl ether carboxylates, acylated peptides, alkyl sulfonates, alkylbenzene and alkylnaphthalene sulfonates, sulfosuccinates, α-olefin sulfonates, N - Acyl sulfonates, alkyl sulfates, alkyl ether sulfates, alkyl allyl ether sulfates, alkylamido sulfates, alkyl phosphates, alkyl ether phosphates, alkyl allyl ether phosphates, and the like.
又、両性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挙げられる。Examples of amphoteric compounds include carboxybetaine, sulfobetaine, aminocarboxylic acid salts, and the like.
特に耐環境性の点でフッ素系のものを用いるのが好まし
く、具体的にはノニオン性のものとしては、バーフルオ
ロアルキル基親油性基含有オリゴマー、バーフルオロア
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
としてはバーフルオロアルキル含有第4級アンモニウム
塩等が挙げられ、アニオン性としてはバーフルオロアル
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が挙げられ、又、両性としてはパー
フルオロアルキルを含有したベタインなどが含まれる。In particular, it is preferable to use fluorine-based materials from the viewpoint of environmental resistance.Specifically, nonionic materials include oligomers containing lipophilic groups of perfluoroalkyl groups, oligomers containing hydrophilic groups of perfluoroalkyl groups, and oligomers containing perfluoroalkyl groups and hydrophilic groups. Examples include alkyl ethylene oxide adducts, cationic examples include quaternary ammonium salts containing perfluoroalkyl, and anionic examples include monovalent metal salts of sulfonic acids and carboxylic acids containing perfluoroalkyl, and phosphoric acid. Examples include esters, and amphoteric examples include betaine containing perfluoroalkyl.
又、第3図b1第4図bにおける上層の樹脂層34−、
44−としては上記の32、42と同様のものを用いる
ことができるが、トナーとの潤電性を上げるために荷電
制御剤等の充填剤を混入することもできる。In addition, the upper resin layer 34- in FIG. 3b1 and FIG. 4b,
As 44-, the same materials as 32 and 42 described above can be used, but a filler such as a charge control agent can also be mixed in order to improve the electrification property with the toner.
これら樹脂と界面活性剤は相溶性の良いものどうしを選
択するのであるが、耐環境性、離型性の点で樹脂として
はフッ素樹脂又はシリコーン樹脂が好ましく、又、界面
活性剤としてはフッ素系の界面活性剤が好ましい。These resins and surfactants are selected to have good compatibility with each other, but in terms of environmental resistance and mold release properties, fluororesin or silicone resin is preferred as the resin, and fluorine-based resins are preferred as the surfactant. surfactants are preferred.
最も好ましくはフッ素又はシリコーン樹脂にフッ素系の
界面活性剤を使用する組合せである。Most preferred is a combination of a fluorine-based or silicone resin and a fluorine-based surfactant.
又、イオン性の界面活性剤とノニオン性の界面活性剤と
の混合併用も可能である。この樹脂層作製にあたっては
スプレー塗布、ディッピング、水蒸気加硫、押し出し加
硫等の適切な工法を採用すればよい。It is also possible to use a mixture of an ionic surfactant and a nonionic surfactant. In preparing this resin layer, an appropriate method such as spray coating, dipping, steam vulcanization, extrusion vulcanization, etc. may be employed.
この界面活性剤の混入量はバインダー樹脂又はゴムの固
形分100ffItli1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。0.1fflffi部以下であると効果が十分現
われず、50重量部以上であると耐摩耗性や耐環境性が
劣る。The amount of the surfactant mixed is preferably 0.1 to 50 parts by weight per 1 part of solid content of the binder resin or rubber. More preferably, it is 0.5 to 20 parts by weight. If the amount is less than 0.1 parts by weight, the effect will not be sufficient, and if it is more than 50 parts by weight, the abrasion resistance and environmental resistance will be poor.
又、トナーとしては、従来公知のものがそのまま使用で
きる。このようなトナーの具体例としては、例えばスチ
レン−n−プチルメタクリレートやエボキシ樹脂などの
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(ニグロシン染料、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材、脂肪
酸金属塩等の潤滑剤などを添加したもの等が挙げられる
。Further, as the toner, conventionally known toners can be used as they are. Specific examples of such toner include fine particles containing a coloring agent in a binder resin such as styrene-n-butyl methacrylate or epoxy resin, and if necessary, a charge control agent (nigrosine dye, basic dyes, etc.)
Examples include those to which a fluidizing agent such as silica, an abrasive material such as silicon carbide, and a lubricant such as a fatty acid metal salt are added.
[実施例]
以下、実施例及び比較例により本発明を詳細に説明する
。[Examples] Hereinafter, the present invention will be explained in detail with reference to Examples and Comparative Examples.
実施例1
銅板に以下の樹脂層形戊或分をディッピングにより塗工
し、100℃71時間の条件下で硬化させて膜厚20μ
mの樹脂層を形成した。Example 1 The following resin layered coating was applied to a copper plate by dipping and cured at 100°C for 71 hours to a film thickness of 20 μm.
m resin layers were formed.
[樹脂層形成成分]
フッ素系共重合体樹脂(ルミフロン
801C.旭硝子製)(固形分50%)100重量部コ
ロネートEH(50%キシレン溶液)20重量部
フッ素系イオン性界面活性剤(カチ
オン性) (EPl32 ;三菱金属製) 5重量
部M E K 400重量部
実施例2
実施例1で用いるイオン性界面活性剤(EPl32)の
代わりに(EF102;三菱金属)(アニオン性)を用
いる他は実施例1と同じとした。[Resin layer forming components] Fluorine-based copolymer resin (Lumiflon 801C, manufactured by Asahi Glass) (solid content 50%) 100 parts by weight Coronate EH (50% xylene solution) 20 parts by weight fluorine-based ionic surfactant (cationic) (EPl32; manufactured by Mitsubishi Metals) 5 parts by weight M E K 400 parts by weight Example 2 The same procedure was carried out except that (EF102; Mitsubishi Metals) (anionic) was used instead of the ionic surfactant (EPl32) used in Example 1. Same as Example 1.
実施例3
実施例1で用いるイオン性界面活性剤(EFl32〉の
代わりにベタイン型両性界面活性剤[フタージエント4
008 .ネオス■]を用いる他は同じとした。Example 3 The ionic surfactant (EFl32) used in Example 1 was replaced with a betaine type amphoteric surfactant [Ftardient 4].
008. The procedure was the same except that Neos ■] was used.
実施例4
銅板に以下の樹脂層形成成分をディッピングにより塗工
し、100℃71時間の条件で硬化させて膜厚20μ1
の樹脂層■を形成した。Example 4 The following resin layer forming components were coated on a copper plate by dipping and cured at 100°C for 71 hours to obtain a film thickness of 20μ1.
A resin layer (2) was formed.
更に、この上に以下の樹脂を同じくスプレー塗布し、1
00℃71時間の条件で硬化させ膜厚20μ園の樹脂層
■を形成した。Furthermore, the following resin was similarly spray applied on top of this, and 1
It was cured at 00° C. for 71 hours to form a resin layer (2) with a thickness of 20 μm.
[樹脂層■形成成分]
フッ素系共重合体樹脂(固形分50%)(ルミフロン6
01C [旭硝子■] )100重量部コロネー}EH
(50%キシレン溶液)20重量部
イオン性界面活性剤(カチオン性)
( E F 132三菱金属) Sff
i量部M E K 400重
量部[樹脂層■形成或分]
フッ素系共重合体樹脂(固形分50%)(ルミフロン8
01C [旭硝子■] )10Offin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
実施例5
実施例4においてイオン性界面活性剤(EF132のか
わりに、EF102三菱金属(アニオン性)を用いる他
は実施例4と同じとした。[Resin layer ■ Forming component] Fluorine copolymer resin (solid content 50%) (Lumiflon 6
01C [Asahi Glass■] ) 100 parts by weight Coronae}EH
(50% xylene solution) 20 parts by weight ionic surfactant (cationic) (EF 132 Mitsubishi Metals) Sff
i part M E K 400 parts by weight [Resin layer ■ formation amount] Fluorine copolymer resin (solid content 50%) (Lumiflon 8
01C [Asahi Glass ■] ) 10 Offin part Coronate EH (50% xylene solution) 20 parts by weight M E K 400 parts by weight Example 5 In Example 4, an ionic surfactant (instead of EF132, EF102 Mitsubishi Metals (anionic) The procedure was the same as in Example 4 except that .
実施例6
実施例4においてイオン性界面活性剤(EFl32〉の
かわりにベタイン型両性界面活性剤[フタージェント4
008 .ネオスW]を用いる他は同じとした。Example 6 In Example 4, a betaine type amphoteric surfactant [Ftergent 4] was used instead of the ionic surfactant (EFl32).
008. The procedure was the same except that Neos W] was used.
比較例1
実施例1におけるイオン性界面活性剤を用いない他は実
施例1と同じとした。Comparative Example 1 The same procedure as Example 1 was carried out except that the ionic surfactant in Example 1 was not used.
比較例2 実施例1における樹脂層を塗布しないものとする。Comparative example 2 Assume that the resin layer in Example 1 is not applied.
以上のようにして得られた実施例及び比較例のトナー薄
層ブレードを第1図における現像装置に用い、以下の評
価をした。The toner thin layer blades of Examples and Comparative Examples obtained as described above were used in the developing device shown in FIG. 1, and the following evaluations were made.
[トナーの帯電量]
下記の負,iB .QS }ナーを用いて第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、■
初期画像時の帯電量
■ 1万枚ランニング後の帯電量を測定した。[Toner charge amount] The following negative, iB. Using a blow-off method, the amount of charge in the developing device shown in Figure 1 was determined using
Charge amount at initial image■ Charge amount after running 10,000 sheets was measured.
(使用トナー)粒径l2μ■
スチレンアクリル樹脂 100重量部
カーボン IO重量部
含クロムモノアゾ染料 2重量部
[トナーのブレード固着]
第1図に示す現像装置において、1万枚ランニング後の
ブレードを取り出して以下によりランクづけした。(Toner used) Particle size 12 μ Styrene acrylic resin 100 parts by weight Carbon IO parts by weight Chromium-containing monoazo dye 2 parts by weight [Toner blade sticking] In the developing device shown in Figure 1, take out the blade after running 10,000 sheets. Ranked according to the following.
ランクA:布などでブレード表面のトナーが簡車にふき
とれる。Rank A: Toner on the blade surface can be wiped off with a cloth or the like.
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ブレード表面に固着
している。Rank D: Melted toner is strongly adhered to the blade surface.
[トナーの帯電量立ち上がり性]
上記と同じ負トナーを用い、第1図に示す現像装置にお
いて、初期状態から現像ローラ1回転駆動後のトナーの
帯電量Q+と5回転後の帯電量Q5を測定した。[Charge rise property of toner] Using the same negative toner as above, in the developing device shown in Fig. 1, the toner charge amount Q+ after driving the developing roller one rotation from the initial state and the charge amount Q5 after 5 rotations were measured. did.
なお、現像ローラ、補給ローラ及び感光体は以下のもの
を使用した。The following developing rollers, replenishment rollers, and photoreceptors were used.
(現像ローラ) 導電性シリコーンゴムに樹脂をコーティングしたもの。(Developing roller) Conductive silicone rubber coated with resin.
(トナー補給ローラ)
導電性ウレタンスポンジ
(感光体)
O P C
表−1
[発明の効果]
以上説明したように、本発明の構或による現像装置によ
れば、長期連続運転においても、トナー規制部材にトナ
ーが固着することなく、又トナー帯電量も適切に長期間
安定であり、安定した画像を得ることができる。(Toner replenishment roller) Conductive urethane sponge (photoreceptor) O P C Table 1 [Effects of the invention] As explained above, according to the developing device according to the structure of the present invention, toner regulation can be achieved even during long-term continuous operation. The toner does not stick to the member, and the toner charge amount remains appropriately stable for a long period of time, making it possible to obtain stable images.
第1図及び第2図は本発明の現像装置を示す概略図、第
3図a1第3図b1第4図a,第4図bは、本発明の現
像装置に用いるトナー規制部材の構成を説明する図。1 and 2 are schematic diagrams showing the developing device of the present invention, and FIG. 3 a1 FIG. 3 b1 FIG. 4 a and FIG. Diagram to explain.
Claims (2)
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、前記規制部材は導電性基体上
に界面活性剤を含有する樹脂層を具備していることを特
徴とする現像装置。(1) An electrostatic latent image holder that holds at least an electrostatic latent image, a toner carrier that makes the latent image visible on the holder, and a regulating member that forms a thin layer of toner on the toner carrier. A developing device comprising: a resin layer containing a surfactant on a conductive substrate;
(1)に記載の現像装置。(2) The developing device according to claim (1), wherein the surfactant is a fluorine-based surfactant.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1307507A JPH03168664A (en) | 1989-11-29 | 1989-11-29 | 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 |
---|---|---|---|
JP1307507A JPH03168664A (en) | 1989-11-29 | 1989-11-29 | Developing device |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03168664A true JPH03168664A (en) | 1991-07-22 |
Family
ID=17969912
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1307507A Pending JPH03168664A (en) | 1989-10-16 | 1989-11-29 | Developing device |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03168664A (en) |
-
1989
- 1989-11-29 JP JP1307507A patent/JPH03168664A/en active Pending
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