JPH03192377A - Developing device - Google Patents
Developing deviceInfo
- Publication number
- JPH03192377A JPH03192377A JP1333555A JP33355589A JPH03192377A JP H03192377 A JPH03192377 A JP H03192377A JP 1333555 A JP1333555 A JP 1333555A JP 33355589 A JP33355589 A JP 33355589A JP H03192377 A JPH03192377 A JP H03192377A
- Authority
- JP
- Japan
- Prior art keywords
- developer
- developing roller
- copolymer
- weight
- developing
- 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
- 229920001577 copolymer Polymers 0.000 claims abstract description 45
- 230000001105 regulatory effect Effects 0.000 claims abstract description 19
- 125000000217 alkyl group Chemical group 0.000 claims description 9
- 125000002947 alkylene group Chemical group 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 125000001453 quaternary ammonium group Chemical group 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 239000003973 paint Substances 0.000 abstract description 15
- 239000007787 solid Substances 0.000 abstract description 8
- 238000000034 method Methods 0.000 abstract description 6
- 238000007598 dipping method Methods 0.000 abstract description 5
- 150000003242 quaternary ammonium salts Chemical class 0.000 abstract description 3
- 239000007921 spray Substances 0.000 abstract description 2
- 239000003085 diluting agent Substances 0.000 abstract 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 14
- 238000012546 transfer Methods 0.000 description 11
- -1 polyethylene Polymers 0.000 description 9
- 238000011161 development Methods 0.000 description 8
- 239000004743 Polypropylene Substances 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 7
- 239000000975 dye Substances 0.000 description 7
- 229920001155 polypropylene Polymers 0.000 description 7
- 229920005989 resin Polymers 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- 239000000377 silicon dioxide Substances 0.000 description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- 239000000654 additive Substances 0.000 description 5
- 230000000996 additive effect Effects 0.000 description 5
- 108091008695 photoreceptors Proteins 0.000 description 5
- 229920001225 polyester resin Polymers 0.000 description 5
- 239000004645 polyester resin Substances 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 229920002379 silicone rubber Polymers 0.000 description 4
- 239000004945 silicone rubber Substances 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 229920006311 Urethane elastomer Polymers 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 3
- 230000007547 defect Effects 0.000 description 3
- 230000006866 deterioration Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229920002635 polyurethane Polymers 0.000 description 3
- 239000004814 polyurethane Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 238000009503 electrostatic coating Methods 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N methyl ethyl ketone Substances CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
- 239000012046 mixed solvent Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- SBYMUDUGTIKLCR-UHFFFAOYSA-N 2-chloroethenylbenzene Chemical compound ClC=CC1=CC=CC=C1 SBYMUDUGTIKLCR-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
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 229920002943 EPDM rubber Polymers 0.000 description 1
- 239000001692 EU approved anti-caking agent Substances 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000013032 Hydrocarbon resin Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229920007962 Styrene Methyl Methacrylate Polymers 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000004581 coalescence Methods 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000011231 conductive filler Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- RMKNCYHVESPYFD-UHFFFAOYSA-N decan-1-amine;hydrochloride Chemical compound [Cl-].CCCCCCCCCC[NH3+] RMKNCYHVESPYFD-UHFFFAOYSA-N 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229920006270 hydrocarbon resin Polymers 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000000696 magnetic material Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- ADFPJHOAARPYLP-UHFFFAOYSA-N methyl 2-methylprop-2-enoate;styrene Chemical compound COC(=O)C(C)=C.C=CC1=CC=CC=C1 ADFPJHOAARPYLP-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001490 poly(butyl methacrylate) polymer Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920002102 polyvinyl toluene Polymers 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 1
- 229920006249 styrenic copolymer Polymers 0.000 description 1
- 238000005211 surface analysis Methods 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Landscapes
- Dry Development In Electrophotography (AREA)
Abstract
Description
【発明の詳細な説明】
[発明の目的]
(産業上の利用分野)
本発明は、電子写真装置において、静電潜像保持体上に
形成された静電潜像を非磁性−成分系現像剤によって可
視像化するのに適した現像装置に関する。Detailed Description of the Invention [Objective of the Invention] (Industrial Field of Application) The present invention is an electrophotographic apparatus in which an electrostatic latent image formed on an electrostatic latent image carrier is developed using a non-magnetic component. The present invention relates to a developing device suitable for visualizing an image using an agent.
(従来の技術)
静電潜像保持体に形成された静電潜像を、非磁性−成分
現像剤によって可視像化する現像装置として、第1図に
要部構成を断面的に示すように構成ないし動作する現像
装置が知られている。すなわち、現像剤(トナー)容器
1に投入された非磁性−成分系現像剤2は、撹拌器3や
現像剤供給ローラー4などにより、現像ローラー5へと
搬送される。現像ローラー5に搬送された現像剤2は、
現像ローラ−5外周面に端部を近接させて配置した現像
剤層厚規制部材6領域を通過することによって、現像ロ
ーラー5の表面に薄層化して保持される一方、規定の電
荷を付与される。このようにして現像ローラー5の表面
上に担持された現像剤により、潜像保持体7に形成され
た静電潜像を電界を利用して現像し、潜像保持体7に記
録された静電気的情報を可視像化する非磁性−成分現像
装置である。(Prior Art) A developing device that visualizes an electrostatic latent image formed on an electrostatic latent image holder using a non-magnetic component developer is shown in FIG. 1 in cross section. A developing device configured and operated as follows is known. That is, a non-magnetic component developer 2 placed in a developer (toner) container 1 is conveyed to a developing roller 5 by an agitator 3, a developer supply roller 4, and the like. The developer 2 conveyed to the developing roller 5 is
By passing through the region of the developer layer thickness regulating member 6 whose end is disposed close to the outer circumferential surface of the developing roller 5, the developer is held in a thin layer on the surface of the developing roller 5, while being given a prescribed electric charge. Ru. The electrostatic latent image formed on the latent image carrier 7 is developed by the developer carried on the surface of the developing roller 5 using an electric field, and the electrostatic charge recorded on the latent image carrier 7 is This is a non-magnetic component developing device that visualizes digital information.
ところで、上記現像ローラー5は、通常、第2図に一部
切欠して斜視的に示す構造をしている。Incidentally, the developing roller 5 usually has a structure shown in perspective with a portion cut away in FIG. 2.
すなわち、たとえば少なくとも外周表面にポリウレタン
樹脂またはポリウレタンエラストマーをバインダーとす
る抵抗値がlO“Ω・備以下の導電性層5aを有し、こ
の導電性層5aの内側に月S規格に8301のA型硬度
計で測定した硬度が40度以下、好ましくは35度以下
の耐油性ゴムからなる弾性体層5hとを具備した構成を
なしている。なお、第2図において5cは金属性ローラ
基体であり、また、前記弾性体層5bを形成する耐油性
ゴムとしては、EPDM、ウレタン、シリコーン、クロ
ロブレン、NBRなどが挙げられ、これらに導電性フィ
ラーを分散させて導電性化した系でもよい。That is, for example, at least on the outer circumferential surface, there is a conductive layer 5a having a resistance value of 10"Ω. It has a structure comprising an elastic layer 5h made of oil-resistant rubber whose hardness measured with a hardness meter is 40 degrees or less, preferably 35 degrees or less.In addition, in FIG. 2, 5c is a metal roller base. Also, examples of the oil-resistant rubber forming the elastic layer 5b include EPDM, urethane, silicone, chloroprene, NBR, etc., and a system in which a conductive filler is dispersed in these to make them conductive may also be used.
(発明が解決しようとする課題)
しかし、上記の現像装置には次のような不具合が認めら
れる。すなわち、前記現像装置に用いられている現像ロ
ーラー5の少なくとも表面には、導電性の塗料をコーテ
ィングして所要の導電性層5a8形成した構成をしてい
る。しかしながら、これら導電性塗料の塗膜の静電気的
帯電性を測定してみると、現像剤と同極性かまたは逆極
性でも帯電能力はほとんどないものが多い。このため、
現像剤に意識的に適正な帯電量を与えることができず、
現像剤こぼれや、付着担持する現像剤層が不均一になる
などの現像剤層不良や搬送不良が起きやすく、実用上十
分な画像を得られない場合が往々ある。(Problems to be Solved by the Invention) However, the following problems are recognized in the above-mentioned developing device. That is, at least the surface of the developing roller 5 used in the developing device is coated with a conductive paint to form a required conductive layer 5a8. However, when measuring the electrostatic chargeability of the coating film of these conductive paints, many of them have almost no charging ability even if they have the same polarity as the developer or the opposite polarity. For this reason,
Unable to consciously apply an appropriate amount of charge to the developer,
Developer layer defects such as developer spillage and non-uniformity of the adhered and carried developer layer and transportation defects are likely to occur, and it is often impossible to obtain images that are sufficient for practical use.
上記現像プロセスにおいては、負帯電性現像剤が用いら
れていること、現像ローラーや現像剤層厚規制部材、中
間ローラーなどの現像剤に摩擦電荷を付与する部材を正
に帯電させることにより、rFJ記現像剤に十分な帯電
を与え得ることに着目した改善策も知られている。たと
えば、溶剤系の塗料を現像ローラーの表面に塗布する系
の現像ローラーの場合、現像ローラーの帯電制御のため
に染料など(たとえば、アジン系のニグロシン、ニグロ
シン塩基類、ニグロシン誘導体、ベンゾメチル−へキシ
ルデシルアンモニウムクロライドなどの有機四級アンモ
ニウム塩など)の帯電制御剤を添加している。しかしこ
れら帯電制御剤のほとんどは溶媒に不溶もしくは微溶で
あるため塗料への分散が容品ではなく、それによって機
能が発現しにくくなり、添加量を増やさざるを得ないと
いう欠点がある。In the above development process, the rFJ Improvement measures are also known that focus on the ability to impart sufficient charge to the developer. For example, in the case of a developing roller that applies a solvent-based paint to the surface of the developing roller, dyes (for example, azine-based nigrosine, nigrosine bases, nigrosine derivatives, benzomethyl-hexyl A charge control agent such as an organic quaternary ammonium salt such as decyl ammonium chloride is added. However, since most of these charge control agents are insoluble or slightly soluble in solvents, they cannot be easily dispersed in paints, which makes it difficult for them to function properly and has the disadvantage that the amount added must be increased.
本発明は、上記の問題を解決するためになされたもので
°、現像ローラーに担持、搬送される現像剤に所要の帯
電量を容易にかつ、常時確実に付与し得るよう構成され
た現像装置の提供を目的とする。The present invention has been made in order to solve the above problems, and is a developing device configured to easily and always reliably apply the required amount of charge to the developer carried and conveyed on the developing roller. The purpose is to provide.
[発明の構成]
(課題を解決するための手段)
本発明は、弾性を有する現像ローラーに現像剤を供給し
、規制部材により前記現像ローラー外周面上に現像剤の
薄層を形成するとともに電荷を与える機構と、この現像
剤薄層を静電潜像担持体に近接または接触させ、前記静
電潜像担持体に保持された静電潜像に現像剤を付着せし
めて可視像に現像する機構とを備えた現像装装置におい
て、前記現像剤に摩擦電荷を付与する現像ローラー規制
部材および現像剤供給手段の少なくともいずれかの表面
に、下記式
で示される繰り返し単位が60〜99mm部と下記式R
s (2)
(式中、R2は水素原子またはアルキル基であり、R3
はアルキレン基であり、R4、R5およびR6はアルキ
ル基であり、このアルキル基およびアルキレン基の炭素
数は1−12である。)で示される繰り返し単位が40
−1!r[ffi部からなる共重合体で、fr量平均分
子量が3oo〜25000の範囲内、好ましくは300
0〜8000の範囲にある第4級アンモニウム塩基含有
共重合体を含有させたことを特徴としている。なお、以
下より上記物質を共重合体と呼ぶことにする。[Structure of the Invention] (Means for Solving the Problems) The present invention supplies a developer to an elastic developing roller, forms a thin layer of the developer on the outer circumferential surface of the developing roller using a regulating member, and also controls the electric charge. and a mechanism for bringing this thin layer of developer close to or in contact with an electrostatic latent image carrier to cause the developer to adhere to the electrostatic latent image held on the electrostatic latent image carrier and develop it into a visible image. In the developing device equipped with a mechanism for applying a frictional charge to the developer, a repeating unit represented by the following formula is formed in a portion of 60 to 99 mm on the surface of at least one of the developer roller regulating member and the developer supplying means that apply a frictional charge to the developer. The following formula R
s (2) (wherein, R2 is a hydrogen atom or an alkyl group, and R3
is an alkylene group, R4, R5 and R6 are alkyl groups, and the alkyl group and alkylene group have 1 to 12 carbon atoms. ) is 40 repeating units
-1! A copolymer consisting of r [ffi part, fr weight average molecular weight within the range of 3oo to 25,000, preferably 300
It is characterized by containing a copolymer containing a quaternary ammonium base in the range of 0 to 8,000. Note that from now on, the above substance will be referred to as a copolymer.
しかして、本発明は上記現像プロセスにおいては、負帯
電性現像剤が用いられていること、現像ローラーや現像
剤層厚規制部材、中間ローラーなどの現像剤に摩擦電荷
を付与する部材を正に帯電させることにより、前記現像
剤に十分な帯電を与え得ることに着目してなされたもの
である。Therefore, in the above-mentioned development process, the present invention requires that a negatively charged developer is used, and that members that impart a triboelectric charge to the developer, such as the developing roller, developer layer thickness regulating member, and intermediate roller, are positively charged. This method was developed based on the fact that the developer can be sufficiently charged by charging the developer.
本発明に係る共重合体は溶媒に易溶であるためハンドリ
ングが容品であるばかりでなく、樹脂系であるため塗料
との分散性、相溶性にも優れ、少量の添加で効果が期待
できるというメリットがある。たとえば、シリコーンゴ
ムよりなる現像剤層厚規制部材に上記本発明に係る共重
合体を含有させる場合、メインバインダーとの相溶性に
優れるために少量の添加で所要の効果を得ることができ
る。The copolymer according to the present invention is not only easy to handle because it is easily soluble in solvents, but also has excellent dispersibility and compatibility with paints because it is resin-based, and can be expected to be effective even when added in small amounts. There is an advantage. For example, when the copolymer according to the present invention is contained in a developer layer thickness regulating member made of silicone rubber, the desired effect can be obtained with a small amount of addition because of its excellent compatibility with the main binder.
また、上記の構造式を持つ第4級アンモニウム塩基含有
共重合体の製法などは、特開昭03−80458号公報
に開示されている。Furthermore, a method for producing a quaternary ammonium base-containing copolymer having the above structural formula is disclosed in JP-A-03-80458.
本発明においては、前記現像ローラーや現像剤層厚規制
部材の表面に前記共重合体を0.01重量部から80重
量部、好ましくはo、imm部がら10重量部含有させ
ることにより、現像ローラーなどの表面摩擦帯電性を改
善するものである。たとえば、導電性塗料を現像ローラ
ーに塗布して用いる場合は、予め導電性塗料の希釈液に
適正量の前記共重合体を溶解させておき、導電性塗料本
体と混合分散し、これを現像ローラーにディッピング、
スプレー ローラー法などを用いて塗布し乾燥して現像
装置へ組み込まれる。ここで塗布された導電性層の膜厚
は5μm〜200μ園の範囲、好ましくは30μtg
−120μmである。また、現像剤層厚規制部材の表面
摩擦帯電性を改善する場合、たとえば、シリコーンゴム
を現像剤層厚規制部材として用いる場合、シリコーンゴ
ムに対して0.01ffiffi部から40重量部、好
ましくはO,1ffi量部から10重量部を添加してニ
ーダ−などの混練機で分散含有させた後、加硫・成形加
工し現像剤層厚規制部材として現像装置へ組み込まれる
。In the present invention, by containing the copolymer in the surface of the developing roller or the developer layer thickness regulating member from 0.01 parts by weight to 80 parts by weight, preferably 10 parts by weight from the o and im parts, the developing roller This improves the surface triboelectrification properties of For example, when applying a conductive paint to a developing roller, an appropriate amount of the copolymer is dissolved in advance in a diluted solution of the conductive paint, mixed and dispersed with the conductive paint body, and this is applied to the developing roller. Dipping,
It is applied using a spray roller method, dried, and incorporated into the developing device. The thickness of the conductive layer applied here is in the range of 5 μm to 200 μm, preferably 30 μtg.
−120 μm. In addition, when improving the surface triboelectrification of the developer layer thickness regulating member, for example, when silicone rubber is used as the developer layer thickness regulating member, 0.01 ffiffi part to 40 parts by weight, preferably O , 1ffi to 10 parts by weight are added and dispersed in a kneader such as a kneader, and then vulcanized and molded to be incorporated into a developing device as a developer layer thickness regulating member.
上記構成の現像装置においては、結着樹脂、色材、帯電
制御剤、ワックス、およびケーキング防止剤などからな
る公知の非磁性−成分系現像剤(トナー)が用いられる
。In the developing device having the above configuration, a known non-magnetic component developer (toner) consisting of a binder resin, a coloring material, a charge control agent, a wax, an anti-caking agent, etc. is used.
たとえば、結着樹脂としては、ポリスチレン、ポリ−2
−クロルスチレン、ポリビニルトルエン等のスチレンお
よびその置換体の単重合体、たとえばスチレン−P−ビ
ニルトルエン共重合体、スチレン−プロピレン共重合体
、スチレン−ビニルトルエン共重合体、スチレン−ビニ
ルナフタレン共重合体、スチレン−アクリル酸メチル共
重合体、スチレン−アクリル酸共重合体、スチレン−ア
クリル酸ブチル共重合体、スチレン−アクリル酸オクチ
ル共重合体、スチレン−メタアクリル酸メチル共重合体
、スチレン−メタアクリル酸エチル共重合体、スチレン
−メタアクリル酸ブチル共重合体、スチレン−メタアク
リル酸オクチル共重合体、スチレン−αクロルメタアク
リル酸メチル共重合体、スチレン−アクリロニトリル共
重合体、スチレン−ビニルメチルエーテル共重合体、ス
チレン−ビニルエチルエーテル共重合体、スチレン−ビ
ニルメチルケトン共重合体、スチレン−ブタジェン共重
合体、スチレンーアクリ口ニトリルーインデン共重合体
、スチレン−イソプレン共重合体、スチレン−マレイン
酸共重合体、スチレン−マレイン酸エステル共重合体等
のスチレン系共重合体、ポリメチルメタクリレート、ポ
リブチルメタクリレート、ポリ塩化ビニル、ポリ酢酸ビ
ニル、ポリエチレン、ポリプロピレン、ポリエステル、
ポリウレタン、ポリアミド、エポキシ樹脂、ポリビニル
ブチラール、ポリアクリル酸樹脂、ロジン、食性ロジン
、テルペン樹脂、フェノール樹脂、脂肪族または脂環族
炭化水素樹脂、芳容族系石油樹脂、塩素化パラフィン、
パラフィンワックスなどが単独あるいは混合物が挙げら
れる。For example, as the binder resin, polystyrene, poly-2
- Homopolymers of styrene and its substituted products such as chlorostyrene and polyvinyltoluene, such as styrene-P-vinyltoluene copolymer, styrene-propylene copolymer, styrene-vinyltoluene copolymer, styrene-vinylnaphthalene copolymer Coalescence, styrene-methyl acrylate copolymer, styrene-acrylic acid copolymer, styrene-butyl acrylate copolymer, styrene-octyl acrylate copolymer, styrene-methyl methacrylate copolymer, styrene-methacrylate copolymer Ethyl acrylate copolymer, styrene-butyl methacrylate copolymer, styrene-octyl methacrylate copolymer, styrene-alpha chloromethyl methacrylate copolymer, styrene-acrylonitrile copolymer, styrene-vinylmethyl Ether copolymer, styrene-vinyl ethyl ether copolymer, styrene-vinyl methyl ketone copolymer, styrene-butadiene copolymer, styrene-acrylic nitrile-indene copolymer, styrene-isoprene copolymer, styrene-maleic acid Copolymers, styrenic copolymers such as styrene-maleic acid ester copolymers, polymethyl methacrylate, polybutyl methacrylate, polyvinyl chloride, polyvinyl acetate, polyethylene, polypropylene, polyester,
Polyurethane, polyamide, epoxy resin, polyvinyl butyral, polyacrylic acid resin, rosin, edible rosin, terpene resin, phenolic resin, aliphatic or alicyclic hydrocarbon resin, aromatic petroleum resin, chlorinated paraffin,
Paraffin wax and the like may be used alone or as a mixture.
また、青色剤、帯電制御剤としてはカーボンブラック、
各種染料顔料などが、オフセット防止剤しては低分子量
のポリエチレン、ポリプロピレンなどが、ケーキング防
止剤としては疎水性シリカ、金属酸化物や、PHMA、
テフロン、スチレンなどの球状樹脂微粒子がそれぞれ挙
げられる。In addition, carbon black is used as a blue agent and charge control agent.
Various dyes and pigments are used, offset inhibitors include low molecular weight polyethylene and polypropylene, and anti-caking agents include hydrophobic silica, metal oxides, PHMA,
Examples include spherical resin particles such as Teflon and styrene.
(作用)
現像剤(トナー)に所要の摩擦電荷を付与する部材、す
なわち現像ローラーおよび現像剤層厚規制部材の少なく
とも一方の表面に前記共重合体を含有させたことにより
、現像に必要な有効な電荷を現像剤に与えることが可能
となり、シャープなライン画像、均一なベタ画像を用意
かつ確実に出力し得るばかりでなく、現像装置の寿命も
延ばすことができる。(Function) By containing the copolymer on the surface of at least one of the members that impart the required triboelectric charge to the developer (toner), that is, the developing roller and the developer layer thickness regulating member, the effective It becomes possible to apply a strong charge to the developer, and not only can sharp line images and uniform solid images be outputted easily and reliably, but also the life of the developing device can be extended.
この共重合体の効果を確認するために、第3図に模式的
に示す静電塗膜表面解析装置(東芝ケミカル社製)で帯
電量の測定を行った。測定条件を25℃、853f[全
部の環境雰囲気に設定し、球状鉄分を用い、流し掛は量
−回あたりt、aog 、流し掛は時間5秒、傾斜勾配
00度、+1−1定点1サンプル5点で測定したところ
、本発明に係る共重合体を未添加のものは80X 10
−!IC以下であったのに対して、本発明に係る共重合
体を添加した物質は80X10−”C以上であり、明ら
かに帯電性が良くなっていることがわかる。In order to confirm the effect of this copolymer, the amount of charge was measured using an electrostatic coating surface analyzer (manufactured by Toshiba Chemical Co., Ltd.) schematically shown in FIG. Measurement conditions were set at 25℃, 853f [all environmental atmospheres were used, spherical iron was used, the amount of pouring was t, aog per time, the time of pouring was 5 seconds, the slope was 00 degrees, and one sample was taken at a +1-1 fixed point. When measured at 5 points, the copolymer according to the present invention was not added at 80X 10
-! In contrast, the material to which the copolymer according to the present invention was added had a chargeability of 80 x 10-''C or more, which clearly shows that the chargeability is improved.
なお、第3図において、15は基準鉄粉投入口、16は
傾斜板(サンプル台)、17は受は皿、19は絶縁板、
20はエレクトロメーター 21はメーター接続端子で
ある。In addition, in FIG. 3, 15 is a standard iron powder inlet, 16 is an inclined plate (sample stand), 17 is a tray, 19 is an insulating plate,
20 is an electrometer and 21 is a meter connection terminal.
(実施例) 次に本発明の詳細な説明する。(Example) Next, the present invention will be explained in detail.
実施例1
0本ミラクトラン社製ポリウレタン導電性塗料スパレッ
クス 100gに、テトラヒドロフランTHP ニーメ
チルエチルケトンMfJ(1:l)混合溶媒longに
上記共重合体(藤倉化成製FCA201−83 )を5
g溶解させた溶媒を混合希釈、分散させた。Example 1 0 100 g of polyurethane conductive paint SPAREX manufactured by Miractran Co., Ltd. was added with 5 liters of the above copolymer (FCA201-83 manufactured by Fujikura Kasei Co., Ltd.) in a long mixed solvent of tetrahydrofuran THP Ni-methyl ethyl ketone MfJ (1:l).
g The dissolved solvent was mixed, diluted, and dispersed.
この混合分散液を現像ローラー(ウレタンゴム)表面に
ディッピング法で塗布した後、乾燥器で20分間乾乾燥
て現像ローラーを作製した。This mixed dispersion was applied to the surface of a developing roller (urethane rubber) by a dipping method, and then dried in a dryer for 20 minutes to produce a developing roller.
かくして得た現像ローラーの表面抵抗は1XlOsΩ・
国であり、また形成された塗膜厚は100μlであった
。The surface resistance of the developing roller thus obtained was 1XlOsΩ・
The thickness of the coating film formed was 100 μl.
上記構成した現像ローラーを、前記第1図に要部構成を
示す現像装置の現像ローラー5と代替し、同様の現像装
置を構成試作して、下記の条件で画出しを行った。The developing roller constructed as described above was substituted for the developing roller 5 of the developing device whose essential structure is shown in FIG.
現像剤2としては、ポリエステル樹脂92重量部、カー
ボン4重量部、低分子量ポリプロピレン2ffI量部、
含金染料2i11量部および外添剤シリカ0.5ffi
ffi部からなる体積平均粒径lOμ■の非磁性−成分
系現像剤を用い、潜像担持体(OPC) 7の回転を表
面速度50mm/Sと設定し、帯電器9からのコロナ放
電で一様に表面電位−500vに帯電し、レー露光器8
としてのレーザーで画像情報を記録した後、表面速度1
0ha/Sで回転させ、かつ、−200Vを印加した現
像ローラー5を潜像担持体(感光体)7に押し当て、所
要の現像を行った。この現像された粉体像を転写装置1
1において、6kvの直流コロナ放電で記録紙へ転写し
た後、熱定着した。As the developer 2, 92 parts by weight of polyester resin, 4 parts by weight of carbon, 2ffI parts of low molecular weight polypropylene,
11 parts of metal-containing dye 2i and 0.5ffi of external additive silica
Using a non-magnetic component developer with a volume average particle diameter of lOμ■ consisting of ffi parts, the rotation of the latent image carrier (OPC) 7 was set at a surface speed of 50 mm/s, and the rotation of the latent image carrier (OPC) 7 was set at a surface speed of 50 mm/s. The surface potential is -500V as shown in FIG.
After recording the image information with a laser as , the surface speed is 1
A developing roller 5 rotated at 0 ha/s and applied with −200 V was pressed against the latent image carrier (photoreceptor) 7 to perform the required development. This developed powder image is transferred to the transfer device 1
In No. 1, the image was transferred onto recording paper using a 6 kV DC corona discharge, and then thermally fixed.
前記転写後の画像は、ライン画像の鮮明な、ベタ画像の
均一な高濃度の画像であった。また、5万枚のライフ試
験後の画像も初期状態を維持した劣化のない鮮明な画像
であった。さらに、高温多湿条件においても極めて良好
な画像が得られた。The image after the transfer was a clear line image, a uniform solid image, and a high density image. Furthermore, the images after the life test of 50,000 sheets were clear images with no deterioration and maintaining the initial state. Furthermore, extremely good images were obtained even under high temperature and high humidity conditions.
実施例2
大泰化工社製導電性塗料エレクトロパック 100gに
、イソシアネート 5gと、トルエン 100g中に前
記本発明に係る共重合体(藤倉化成製FCA201−B
3)を5g溶解させた溶媒を混合希釈、分散した。この
混合分散液を現像ローラー(ウレタンゴム)表面にディ
ッピング法で塗布した後、乾燥器で20分間乾燥して現
像ローラーを作製した。かくして得た現像ローラーの表
面抵抗は2XlO’Ω・(至)であり、形成した塗膜厚
は100μ−であった。Example 2 100 g of conductive paint Electropack manufactured by Taitai Kako Co., Ltd., 5 g of isocyanate, and 100 g of toluene were mixed with the copolymer according to the present invention (FCA201-B manufactured by Fujikura Kasei Co., Ltd.).
A solvent in which 5 g of 3) was dissolved was mixed, diluted, and dispersed. This mixed dispersion was applied to the surface of a developing roller (urethane rubber) by a dipping method, and then dried for 20 minutes in a dryer to produce a developing roller. The surface resistance of the developing roller thus obtained was 2XlO'Ω·(max.), and the thickness of the coating film formed was 100 μ−.
上記構成した現像ローラーを、前記第1図に要部構成を
示す現像装置の現像ローラー5に代替し、同様の現像装
置を構成試作して、下記の条件で画出しを行った。The developing roller constructed as described above was replaced with the developing roller 5 of the developing device whose essential structure is shown in FIG.
現像剤2としては、ポリエステル樹脂92ff(EiL
部、カーボン4ffxjli1部、低分子量ポリプロピ
レン2重量部、含金染料2LEiL部および外添剤シリ
カ0.5重量部からなる体積平均粒径lOμ−の非磁性
−成分系現像剤2を用い、潜像担持体(OPC) 7の
回転を表面速度50mm/Sと設定し、帯電器9からの
コロナ放電で一様に表面電位−500vに帯電し1、露
光機8としてのレーザーで画像情報を記録後、表面速度
100m1l/Sテ回転させ、かつ、−200Vを印加
した現像ローラー5を潜像担持体(感光体)7に押し当
て、所要の現像を行った。上記現像された粉体を転写装
置11において6kVの直流コロナ放電で記録紙へ転写
した後、熱定着した。As developer 2, polyester resin 92ff (EiL
A latent image was formed using a non-magnetic component developer 2 with a volume average particle diameter of lOμ, which was composed of 1 part of carbon, 1 part of carbon 4ffxjli, 2 parts of low molecular weight polypropylene, 2LEiL parts of a metal-containing dye, and 0.5 parts by weight of silica as an external additive. The rotation of the carrier (OPC) 7 was set at a surface speed of 50 mm/s, the surface potential was uniformly charged to -500 V by corona discharge from the charger 9, and image information was recorded using a laser as the exposure device 8. A developing roller 5 rotated at a surface speed of 100 ml/S and applied with −200 V was pressed against the latent image carrier (photoreceptor) 7 to perform the required development. The developed powder was transferred to recording paper using a 6 kV DC corona discharge in the transfer device 11, and then thermally fixed.
前記転写後の画像は、ライン画像の鮮明な、ベタ画像の
均一な高濃度の画像であった。また、5万枚のライフ試
験後の画像も初期状態を維持した劣化のない鮮明な画像
であった。さらに、高温多湿条件においても極めて良好
な画像が得られた。The image after the transfer was a clear line image, a uniform solid image, and a high density image. Furthermore, the images after the life test of 50,000 sheets were clear images with no deterioration and maintaining the initial state. Furthermore, extremely good images were obtained even under high temperature and high humidity conditions.
比較例1
日本ミラクトラン社製ポリウレタン導電性塗料スバレッ
クス 100gを、TIIF: MEK (1: l
)混合溶媒longで希釈分散し、これを現像ローラ
ー(ウレタンゴム)表面にディッピング法で塗布した後
、乾燥器で20分間乾燥して現像ローラーを作製した。Comparative Example 1 100 g of polyurethane conductive paint Subalex manufactured by Nippon Miractran Co., Ltd. was mixed with TIIF: MEK (1: l
) The mixture was diluted and dispersed in a long mixed solvent, applied to the surface of a developing roller (urethane rubber) by a dipping method, and then dried in a dryer for 20 minutes to produce a developing roller.
かくして得た現像ローラーの表面抵抗は3、lX1O’
Ω・備であり、形成した塗膜厚は 105μ厳であった
。The surface resistance of the developing roller thus obtained was 3, lX1O'
The coating thickness was exactly 105μ.
上記構成した現像ローラー5を用い、前記第1図に要部
構成を示す現像装置と同様の現像装置を構成試作した、
下記の条件で画出しを行った。Using the developing roller 5 configured as described above, a developing device having the same configuration as the developing device whose main part configuration is shown in FIG.
Image printing was performed under the following conditions.
現像剤としては、ポリエステル樹脂92重量部、カーボ
ン4重量部、低分子量ポリプロピレン2ffi量部、含
金染料2重量部および外添剤シリカ0.5重量部からな
る体積平均粒径lOμ−の非磁性−成分系現像剤2を用
い、潜像担持体(OPC) 7の回転を表面速度50w
/Sと設定し、帯電器9からのコロナ放電で一様に表面
電位−500vに帯電し、露光機8としてのレーザーで
画像情報を記録後、表面速度100m+*/Sで回転さ
せ、かつ、−200を印加した現像ローラー5を潜像担
持体(感光体)7に押し当て、所要の現像を行った。こ
の現像された粉体像を転写装置11において6kvの直
流コロナ放電で記録紙へ転写した後、熱定むした。The developer is a non-magnetic material with a volume average particle diameter of lOμ-, consisting of 92 parts by weight of polyester resin, 4 parts by weight of carbon, 2 parts by weight of low molecular weight polypropylene, 2 parts by weight of gold-containing dye, and 0.5 parts by weight of silica as an external additive. - Using the component-based developer 2, rotate the latent image carrier (OPC) 7 at a surface speed of 50 W.
/S, uniformly charged to a surface potential of -500V by corona discharge from the charger 9, and after recording image information with a laser as the exposure device 8, rotated at a surface speed of 100m+*/S, and The developing roller 5 to which -200 was applied was pressed against the latent image carrier (photoreceptor) 7 to perform the required development. The developed powder image was transferred to a recording paper using a 6 kV DC corona discharge in a transfer device 11, and then heat-set.
前記転写後の画像は、ライン画像の鮮明は鮮明であった
ものの、ベタ画像のは不均一な搬送不良を呈した画像で
あった。In the image after the transfer, although the line image was clear, the solid image was uneven and had poor conveyance.
実施例3
シリコーンゴム1000.当り、上記共重合体(藤倉化
成製PCA201−83 ) 50gおよびアエロジル
状シリカ 150.を加え、ニーダ−で20分間、12
0℃で混練してから、ベンゾイルパーオキサイド10g
を添加して150℃で20分間、200℃で4時間加硫
した。これを金属治具に成形加工して現像剤層厚規制部
材を構成した。Example 3 Silicone rubber 1000. 50 g of the above copolymer (PCA201-83 manufactured by Fujikura Kasei) and 150 g of aerosilic silica. and kneader for 20 minutes, 12
After kneading at 0℃, add 10g of benzoyl peroxide.
was added and vulcanized at 150°C for 20 minutes and at 200°C for 4 hours. This was molded into a metal jig to constitute a developer layer thickness regulating member.
上記現構成した現像剤層厚規制部材を、前記第1図に要
部構成を示す現像装置の現像剤層厚規制部材6と代替し
、同様の現像装置を構成作製して、下記の条件で画出し
を行った。The developer layer thickness regulating member configured above was replaced with the developer layer thickness regulating member 6 of the developing device whose main part configuration is shown in FIG. I made an image.
現像剤2としては、ポリエステル樹脂92重量部、カー
ボン4重量部、低分子量ポリプロピレン2重量部、含金
染料2irIm部および外添剤シリカ0.5fflli
部からなる体積平均粒径lOμ■の非磁性−成分系現像
剤を用い、潜像担持体(OPC’) 7の回転を表面速
度5ha/Sと設定し、帯電器9からのコロナ放電で一
様に表面電位−500vに帯電し、露光器8としてのレ
ーザーで画像情報を記録後、表面速度100−■/Sで
回転させ、かつ、−200Vを印加した現像ローラー5
を潜像担持体(感光体)7に押し当て、所要の現像を行
った。この現像された粉体像を転写装置11において8
kVの直流コロナ放電で記録紙へ転写した後、熱定着し
た。Developer 2 includes 92 parts by weight of polyester resin, 4 parts by weight of carbon, 2 parts by weight of low molecular weight polypropylene, 2 parts by weight of metal-containing dye, and 0.5 parts by weight of silica as an external additive.
Using a non-magnetic component developer with a volume average particle diameter of 10 μι, the rotation of the latent image carrier (OPC') 7 was set at a surface speed of 5 ha/s, and the corona discharge from the charger 9 was used. The developing roller 5 was charged to a surface potential of -500V as shown in FIG.
was pressed against the latent image carrier (photoreceptor) 7 to perform the required development. This developed powder image is transferred to the transfer device 11 at 8
The image was transferred to recording paper using kV direct current corona discharge and then thermally fixed.
前記転写後の画像は、ライン画像の鮮明な、ベタ画像の
均一な高濃度の画像であった。また、5万枚のライフ試
験後の画像も初期状態を維持した劣化のない鮮明な画像
であった。さらに、高温多湿条件においても極めて良好
な画像が得られた。The image after the transfer was a clear line image, a uniform solid image, and a high density image. Furthermore, the images after the life test of 50,000 sheets were clear images with no deterioration and maintaining the initial state. Furthermore, extremely good images were obtained even under high temperature and high humidity conditions.
比較例2
上記実施例3において、シリコーンゴムに前記共重合体
を含有させなかった材料で同じように現像剤層厚規制部
材を作製した。Comparative Example 2 A developer layer thickness regulating member was produced in the same manner as in Example 3 above using a material in which the silicone rubber did not contain the copolymer.
上記現像剤層厚規制部材を用い、前記第1図に要部構成
を示す現像装置と同禄の現像装置を構成試作して、下記
の条件で画出しを行った。Using the above-mentioned developer layer thickness regulating member, a prototype developing device of the same size as the developing device shown in FIG. 1 was constructed, and images were produced under the following conditions.
現像剤2としては、ポリエステル樹脂92ffI m部
、カーボン4重量部、低分子量ポリプロピレン2ffi
量部、含金染料2ffI量部および外添剤シリカ0.5
ffl量部からなる体積平均粒径lOμmの非磁性−成
分系現像剤を用い、潜像担持体(OPC) 7の回転を
表面速度50mm/Sと設定し、帯Th器9からのコロ
ナ放電で一様に表面電位−500Vに帯電し、露光器8
としてのレーザーで画像情報を記録後、表面速度100
■―/Sで回転させ、かつ、−200Vを印加した現像
ローラー5を潜像担持体(感光体)7に押し当て、所要
の現像を行った。この現像された粉体像を転写装置11
において、8kVの直流コロナ放電で記録紙へ転写した
後、熱定着した。As developer 2, 92 ffI m parts of polyester resin, 4 parts by weight of carbon, and 2 ffi low molecular weight polypropylene were used.
parts, 2ffI parts of metal-containing dye, and 0.5 parts of external additive silica.
Using a non-magnetic component developer with a volume average particle diameter of lOμm consisting of ffl amount parts, the rotation of the latent image carrier (OPC) 7 was set at a surface speed of 50 mm/S, and the corona discharge from the band Th device 9 was used. The surface potential is uniformly charged to -500V, and the exposure device 8
After recording image information with a laser, the surface speed is 100
(2) The developing roller 5 rotated at -/S and applied with -200 V was pressed against the latent image carrier (photoreceptor) 7 to perform the required development. This developed powder image is transferred to a transfer device 11
After transferring to recording paper using 8 kV DC corona discharge, the image was thermally fixed.
前記転写後の画像は、ライン画像の鮮明は鮮明であった
ものの、ベタ画像は不均一な搬送不良を呈した画像であ
った。In the image after the transfer, although the line image was clear, the solid image was an image with non-uniform conveyance defects.
なお、上記においては現像ローラーまたは現像剤層厚規
制部材のいずれか一方に、上記共重合体を含有させた構
成を示したが、両者に上記共重合体を含有させた構成と
してもよい。要するに使用する現像剤に所要の摩擦電荷
を付与する役割をなす構成部材の少くともいずれか一つ
に、本発明に係る共重合体を含有させた構成とすればよ
く、たとえば現像剤供給ローラでもよい。また前記共重
合体の含有領域は、摩擦電荷の付与に関与する表面部だ
けでもよい。In addition, although the structure in which the above-mentioned copolymer is contained in either the developing roller or the developer layer thickness regulating member is shown above, it is also possible to have a structure in which both of them contain the above-mentioned copolymer. In short, the copolymer according to the present invention may be contained in at least one of the constituent members that play the role of imparting the required triboelectric charge to the developer used, for example, the developer supply roller may also be used. good. Further, the copolymer-containing region may be only the surface portion that is involved in imparting a triboelectric charge.
[発明の効果]
上記説明したように、現像剤に摩擦電荷を付与する役割
をなす構成部材の少なくとも表面に、下記式
で示される繰り返し単位が60〜99ffi[m部と下
記式(式中、R2は水素原子またはアルキル基であり、
R3はアルキレン基であり、R4、RsおよびR6はア
ルキル基である。)
で示される繰り返し単位が40〜1重瓜部からなる共重
合体で、ffl平均分子量が300〜25000の範囲
内、好ましくは3000〜8000の範囲にある第4級
アンモニウム塩基含有共重合体を含有させたことにより
、現像特性の鮮明な、ベタ画像の均一な高濃度の画像を
常にまた容易に得ることが可能となった。しかも、長期
間にわたり前記所要の機能を保持できることなど、環境
による現像剤の特性変化にも対応できるなど、実用上多
くの利点をもたらすものといえる。[Effects of the Invention] As explained above, at least the surface of the component that plays the role of imparting a triboelectric charge to the developer contains 60 to 99 ffi [m parts of the repeating unit represented by the following formula and the following formula (in the formula, R2 is a hydrogen atom or an alkyl group,
R3 is an alkylene group, and R4, Rs and R6 are alkyl groups. ) A quaternary ammonium base-containing copolymer in which the repeating unit shown by By including it, it has become possible to always and easily obtain uniform, solid, high-density images with clear development characteristics. Moreover, it can be said that it brings about many practical advantages, such as being able to maintain the above-mentioned required functions for a long period of time, and being able to cope with changes in the properties of the developer due to the environment.
第1図は現像装置の要部構成を示す断面図、第2図は現
像ローラーの構成を示す一部切欠斜視図、第3図は帯電
量測定用の静電式塗膜表面解析装置の原理図である。
1・・・・・・・・・現像剤容器
2・・・・・・・・・現像剤
3・・・・・・・・・撹拌器
4・・・・・・・・・現像剤供給ローラー5a・・・・
・・現像ローラー
5b・・・・・・導電性層
6・・・・・・・・・弾性体層
7・・・・・・・・・潜像保持体
8・・・・・・・・・露光器
9・・・・・・・・・帯電器
0・・・・・・・・・クリーニングユニット・・・・・
・・・転写装置
2・・・・・・・・・リカバリブレード3・・・・・・
・・・保護抵抗
4・・・・・・・・・直流電源
トFigure 1 is a cross-sectional view showing the configuration of the main parts of the developing device, Figure 2 is a partially cutaway perspective view showing the configuration of the developing roller, and Figure 3 is the principle of an electrostatic coating surface analysis device for measuring the amount of charge. It is a diagram. 1...Developer container 2...Developer 3...Stirrer 4...Developer supply Roller 5a...
Developing roller 5b... Conductive layer 6... Elastic layer 7... Latent image holder 8...・Exposure unit 9...Charger 0...Cleaning unit...
...Transfer device 2...Recovery blade 3...
...Protection resistor 4...DC power supply
Claims (1)
に現像剤を供給する現像剤供給手段と、前記現像ローラ
ー外周面に端部が近接して供給された現像剤を薄層化す
るとともに電荷を与える規制部材と、前記薄層化された
現像剤層に近接ないし接触して保持する静電潜像を可視
像に現像する静電潜像保持体とを具備する現像装置にお
いて、前記現像剤に摩擦電荷を付与する現像ローラー、
規制部材および現像剤供給手段の少なくともいずれかの
表面が、下記式 ▲数式、化学式、表等があります▼(1) (式中、R_1は水素原子またはアルキル基である)で
示される繰り返し単位が60〜99重量部と下記式▲数
式、化学式、表等があります▼(2) (式中、R_2は水素原子またはアルキル基であり、R
_3はアルキレン基であり、R_4、R_5およびR_
6はアルキル基であり、アルキル基およびアルキレン基
の炭素数は1〜12である。) で示される繰り返し単位が40〜1重量部からなる共重
合体で、重量平均分子量が300〜25000の範囲に
ある第4級アンモニウム塩基含有共重合体を含有するこ
とを特徴とする現像装置。[Scope of Claims] A developing roller having elasticity, a developer supply means for supplying a developer to the outer circumferential surface of the developing roller, and a thin layer of the developer supplied with an end close to the outer circumferential surface of the developing roller. A developing device comprising: a regulating member that applies an electric charge at the same time that the developer layer is thinned; and an electrostatic latent image holder that develops an electrostatic latent image held in close proximity to or in contact with the thinned developer layer into a visible image. A developing roller that applies a triboelectric charge to the developer;
The surface of at least one of the regulating member and the developer supplying means has a repeating unit represented by the following formula ▲ There is a mathematical formula, chemical formula, table, etc. ▼ (1) (In the formula, R_1 is a hydrogen atom or an alkyl group) 60 to 99 parts by weight and the following formula ▲ Numerical formulas, chemical formulas, tables, etc. ▼ (2) (In the formula, R_2 is a hydrogen atom or an alkyl group, and R
_3 is an alkylene group, R_4, R_5 and R_
6 is an alkyl group, and the alkyl group and alkylene group have 1 to 12 carbon atoms. ) A developing device comprising a quaternary ammonium base-containing copolymer containing 40 to 1 part by weight of repeating units represented by the following formula and having a weight average molecular weight in the range of 300 to 25,000.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1333555A JP2955310B2 (en) | 1989-12-22 | 1989-12-22 | Developing device |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1333555A JP2955310B2 (en) | 1989-12-22 | 1989-12-22 | Developing device |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH03192377A true JPH03192377A (en) | 1991-08-22 |
JP2955310B2 JP2955310B2 (en) | 1999-10-04 |
Family
ID=18267351
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1333555A Expired - Lifetime JP2955310B2 (en) | 1989-12-22 | 1989-12-22 | Developing device |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2955310B2 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0878744A2 (en) * | 1997-05-12 | 1998-11-18 | Lexmark International, Inc. | Abrasive shim compliant doctor blade |
US6154625A (en) * | 1997-12-19 | 2000-11-28 | Canon Kabushiki Kaisha | Developing apparatus, apparatus unit, and image forming method |
JP2007316284A (en) * | 2006-05-25 | 2007-12-06 | Canon Inc | Developing roller, process cartridge for electrophotographic device and electrophotographic device |
US8913930B2 (en) | 2011-06-29 | 2014-12-16 | Canon Kabushiki Kaisha | Developing roller, electrophotographic process cartridge, and electrophotographic image forming apparatus |
US10331054B2 (en) | 2016-05-11 | 2019-06-25 | Canon Kabushiki Kaisha | Electrophotographic member, process cartridge and electrophotographic image forming apparatus |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4494518B1 (en) | 2008-12-24 | 2010-06-30 | キヤノン株式会社 | Developer carrier and developing device |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61149969A (en) * | 1984-12-18 | 1986-07-08 | ゼロツクス コーポレーシヨン | Improved toner composition |
JPS6224280A (en) * | 1985-07-25 | 1987-02-02 | Fuji Xerox Co Ltd | Developing device |
-
1989
- 1989-12-22 JP JP1333555A patent/JP2955310B2/en not_active Expired - Lifetime
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61149969A (en) * | 1984-12-18 | 1986-07-08 | ゼロツクス コーポレーシヨン | Improved toner composition |
JPS6224280A (en) * | 1985-07-25 | 1987-02-02 | Fuji Xerox Co Ltd | Developing device |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0878744A2 (en) * | 1997-05-12 | 1998-11-18 | Lexmark International, Inc. | Abrasive shim compliant doctor blade |
EP0878744A3 (en) * | 1997-05-12 | 1999-01-13 | Lexmark International, Inc. | Abrasive shim compliant doctor blade |
US6154625A (en) * | 1997-12-19 | 2000-11-28 | Canon Kabushiki Kaisha | Developing apparatus, apparatus unit, and image forming method |
JP2007316284A (en) * | 2006-05-25 | 2007-12-06 | Canon Inc | Developing roller, process cartridge for electrophotographic device and electrophotographic device |
US8913930B2 (en) | 2011-06-29 | 2014-12-16 | Canon Kabushiki Kaisha | Developing roller, electrophotographic process cartridge, and electrophotographic image forming apparatus |
US10331054B2 (en) | 2016-05-11 | 2019-06-25 | Canon Kabushiki Kaisha | Electrophotographic member, process cartridge and electrophotographic image forming apparatus |
Also Published As
Publication number | Publication date |
---|---|
JP2955310B2 (en) | 1999-10-04 |
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