JP3403848B2 - Paint composition, developing device, and method of manufacturing developing device - Google Patents

Paint composition, developing device, and method of manufacturing developing device

Info

Publication number
JP3403848B2
JP3403848B2 JP05412095A JP5412095A JP3403848B2 JP 3403848 B2 JP3403848 B2 JP 3403848B2 JP 05412095 A JP05412095 A JP 05412095A JP 5412095 A JP5412095 A JP 5412095A JP 3403848 B2 JP3403848 B2 JP 3403848B2
Authority
JP
Japan
Prior art keywords
coating composition
developing device
developing roller
component
latent image
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.)
Expired - Fee Related
Application number
JP05412095A
Other languages
Japanese (ja)
Other versions
JPH08245925A (en
Inventor
三長 斉藤
宏一 常見
泰 真常
之弘 大杉
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Toshiba Corp
Toshiba TEC Corp
Original Assignee
Toshiba Corp
Toshiba TEC Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Toshiba Corp, Toshiba TEC Corp filed Critical Toshiba Corp
Priority to JP05412095A priority Critical patent/JP3403848B2/en
Publication of JPH08245925A publication Critical patent/JPH08245925A/en
Application granted granted Critical
Publication of JP3403848B2 publication Critical patent/JP3403848B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Landscapes

  • Dry Development In Electrophotography (AREA)
  • Developing Agents For Electrophotography (AREA)
  • Paints Or Removers (AREA)
  • Developing For Electrophotography (AREA)

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は塗料組成物に係り、さら
に詳しくはゲル化を抑制・防止し、使用可能時間の長期
化を図った塗料組成物に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a coating composition, and more particularly to a coating composition which suppresses / prevents gelation and prolongs usable time.

【0002】[0002]

【従来の技術】周知のように、塗料は美観,耐候性,耐
汚染性もしくは耐蝕性などを付与するため、各種基材の
表面に塗布される形態で、広く様々な分野で実用化され
ている。そして、この種の塗料(塗料組成物)のうち、
たとえばポリエステル系エラストマー,ビニル系エラス
トマーなどの熱可塑性エラストマーを樹脂成分とし、こ
の樹脂成分を有機溶剤に溶解させて成る一液型の塗料組
成物は、基本的に、塗膜の形成に化学反応を伴わない。
したがって、一般的に、塗料の調製や取扱などもし易い
うえ、貯蔵安定性も比較的良好なので、多くの関心が寄
せられている。なお、前記熱可塑性エラストマーとして
は、その他、用途もしくは使用態様に対応して、スチレ
ン系エラストマー,オレフィン系エラストマー,ポリア
ミド系エラストマー,ウレタン系エラストマー、もしく
はこれらの2種以上から成る共重合体などを樹脂成分と
する塗料組成物も知られている。
2. Description of the Related Art As is well known, paints are applied to the surface of various base materials in order to impart aesthetics, weather resistance, stain resistance or corrosion resistance, and are widely used in various fields. There is. And, of this kind of paint (paint composition),
For example, a one-pack type coating composition obtained by using a thermoplastic elastomer such as a polyester elastomer or a vinyl elastomer as a resin component and dissolving the resin component in an organic solvent basically causes a chemical reaction to form a coating film. Not accompanied.
Therefore, in general, the paint is easy to prepare and handle, and the storage stability is relatively good. In addition, as the thermoplastic elastomer, a resin such as a styrene-based elastomer, an olefin-based elastomer, a polyamide-based elastomer, a urethane-based elastomer, or a copolymer composed of two or more of them may be used as a resin, depending on the use or the mode of use. A coating composition as a component is also known.

【0003】また、潜像保持体に形成した静電潜像など
を、この潜像保持体に対向して配設された現像ローラに
担持させたトナーで現像する機構を備えた現像装置にお
いては、前記現像ローラとしてウレタン,ナイロンなど
のエラストマーで構成されている。この構成は機械的強
度の点ではすぐれている反面、経時的に特性が劣化する
という問題点がある。たとえば、トナーが現像ローラ面
に固着して、トナーの帯電量低下を招来するので、画像
劣化を生じるという問題があった。
Further, in a developing device provided with a mechanism for developing an electrostatic latent image formed on a latent image holding member with toner carried on a developing roller arranged facing the latent image holding member. The developing roller is made of an elastomer such as urethane or nylon. This structure is excellent in mechanical strength, but has a problem that the characteristics deteriorate with time. For example, the toner adheres to the surface of the developing roller, causing a decrease in the amount of charge of the toner, which causes a problem of image deterioration.

【0004】[0004]

【発明が解決しようとする課題】前記したように、熱可
塑性エラストマーは、塗膜形成時に化学反応を伴わない
ため、比較的良好な貯蔵安定性を有するとはいえ、常温
程度以下の温度で比較的容易にゲル状化する場合があ
る。たとえば、フッ素系エラストマーを樹脂成分とした
塗料組成物の場合、常温(室温)で数10時間程度の放置
でゲル化が認められ、10℃程度の低温度では数時間程度
の放置でゲル化が起こり、その用途が実質的に大きく制
約されている。すなわち、フッ素系エラストマーの塗膜
は、耐候性および耐汚染性がすぐれているため、たとえ
ば屋根や橋など外気に直接暴される建築構造材用、ある
いはオゾンなどに暴され易い複写機の現像ローラ用など
への適用が期待されている。しかしながら、フッ素系エ
ラストマーを樹脂成分とする塗料組成物は、その調製
後、比較的短時間でゲル化が起こり始め、一様な塗膜の
形成が困難となり、また、顔料など分散させた塗料組成
物では、顔料の凝集によって、前記一様な塗膜の形成が
さらに困難となるなど、使用可能時間が短いので、前記
のような特長を有しながら実用化が阻まれている。
As described above, the thermoplastic elastomer has relatively good storage stability because it does not undergo a chemical reaction at the time of forming a coating film. In some cases, it easily gels. For example, in the case of a coating composition using a fluoroelastomer as a resin component, gelation is observed after standing for several tens of hours at room temperature (room temperature), and gelation occurs after standing for several hours at a low temperature of about 10 ° C. It occurs and its use is substantially constrained. That is, since the coating film of the fluorine-based elastomer has excellent weather resistance and stain resistance, it is used, for example, for building structural materials such as roofs and bridges that are exposed directly to the outside air, or developing rollers for copying machines that are easily exposed to ozone and the like. It is expected to be applied to applications. However, a coating composition containing a fluoroelastomer as a resin component starts gelation in a relatively short time after its preparation, making it difficult to form a uniform coating film. In the case of a product, the agglomeration of the pigment makes it more difficult to form the uniform coating film, and the usable time is short.

【0005】いずれにしても、塗料組成物の貯蔵安定
性、塗膜の一様性などは、塗料組成物を構造基材の外装
・塗装剤とした場合、その実用性から強く求められるも
のであり、この点従来の塗料組成物においては、樹脂成
分が熱硬化性樹脂である場合、もしくは熱可塑性エラス
トマーであっても、十分満足し得るとはいい難い。
In any case, the storage stability of the coating composition, the uniformity of the coating film, etc. are strongly demanded from the practicality when the coating composition is used as an exterior / coating agent for a structural base material. However, in this respect, it is difficult to say that the conventional coating composition is sufficiently satisfactory even when the resin component is a thermosetting resin or even when it is a thermoplastic elastomer.

【0006】本発明は、上記事情に対処してなされたも
ので、調製後における常温放置でのゲル化などが抑制さ
れ、使用可能時間が大幅に増大された塗料組成物の提供
を目的とする。
The present invention has been made in consideration of the above circumstances, and an object thereof is to provide a coating composition in which gelation of the composition after standing at room temperature is suppressed and the usable time thereof is significantly increased. .

【0007】また、本発明は、長時間用いても特性劣化
のない現像ローラを具備した現像装置および現像装置の
製造方法の提供を目的とする。
It is another object of the present invention to provide a developing device equipped with a developing roller that does not deteriorate in characteristics even when used for a long time, and a method of manufacturing the developing device.

【0008】[0008]

【課題を解決するための手段】本発明に係る塗料組成物
は、フッ素系エラストマーを主成分とし、ポリビニルピ
ロリドンを含む樹脂成分と有機溶剤成分とを組成分とし
て調製された塗料組成物であって、前記樹脂成分の0.
01〜50質量%をポリビニルピロリドンが占めている
ことを特徴とする。
A coating composition according to the present invention comprises a fluorine-based elastomer as a main component and a polyvinyl pigment.
A coating composition prepared by using a resin component containing loridone and an organic solvent component as components, wherein
Polyvinylpyrrolidone occupies 01 to 50 mass%.

【0009】[0009]

【0010】本発明は、次のような論理および実験・検
討に基づいて達成されたものである。すなわち、高分子
溶液におけるゲル化現象は、一般的に溶液中の粒子(分
子)が互いに絡み合い、3次元の網状もしくは蜂の巣状
のような構造を採ることによって発生すると考えられて
いる。このような推理に立つと、高分子溶液中の分子鎖
同士の絡み付きを阻害する物質を共存させればよいこと
になる。このような観点に立って、本発明者らは鋭意検
討を進めた結果、フッ素系エラストマーと、このフッ素
系エラストマーを溶解する有機溶剤とを必須成分として
成る塗料組成物において、所定量のポリビニルピロリド
ンを樹脂成分として、さらに溶解混在させたとき、前記
塗料組成物のゲル化現象が容易に抑制・防止され、調製
後において安定した塗料組成物として機能することを確
認し、本発明に到達したものである。
The present invention has been accomplished on the basis of the following logic and experiment / examination. That is, it is considered that the gelation phenomenon in the polymer solution is generally caused by the particles (molecules) in the solution being entangled with each other and having a three-dimensional net-like or honeycomb-like structure. Based on this reasoning, a substance that inhibits the entanglement of molecular chains in the polymer solution may coexist. From such a viewpoint, the inventors of the present invention have made extensive studies, and as a result, in a coating composition including a fluorine-based elastomer and an organic solvent that dissolves the fluorine-based elastomer as an essential component, a predetermined amount of polyvinylpyrrolidone. As a resin component, when further mixed and dissolved, it was confirmed that the gelation phenomenon of the coating composition is easily suppressed / prevented, and that it functions as a stable coating composition after preparation, and the present invention has been achieved. Is.

【0011】より具体的には、ポリフッ化ビニリデン,
ポリビニリデンフルオライド,ヘキサフルオロプロピレ
ン−テトラフルオロエチレン−ビニリデンフルオライド
共重合体,変性フッ素樹脂、ポリスチレン,ポリp-クロ
ロスチレン,ポリビニルトルエンなどのスチレンもしく
はその置換体の重合体などが挙げられる。そして、これ
ら有機バインダーのうち、有機溶剤に難溶解性の有機バ
インダーを主たる樹脂成分とする場合、本発明は特に有
効である。
More specifically, polyvinylidene fluoride,
Examples thereof include polyvinylidene fluoride, hexafluoropropylene-tetrafluoroethylene-vinylidene fluoride copolymer, modified fluororesin, polystyrene, poly-p-chlorostyrene, and polymers of styrene such as polyvinyltoluene or a substitution product thereof. Then, of these organic binders, the present invention is particularly effective when the main resin component is an organic binder that is hardly soluble in an organic solvent.

【0012】本発明において、特に次式−CO−N =で示
される結合を分子中に有するポリビニルピロリドンがゲ
ル化防止に有効であった。ここで、含窒素ビニル重合体
の重合度は、溶解性を考慮した場合、高々20万程度であ
り、好ましくは 100〜 8万程度である。そして、この含
窒素ビニル重合体の組成比は、塗料組成物の有機バイン
ダーを含む樹脂成分中の0.01〜50質量%、好ましくは
0.1〜10質量%、さらに望ましくは 0.5〜 5質量%であ
る。なお、含窒素ビニル重合体の組成比が、0.01質量%
未満では添加・配合の効果が認められず、また、50質量
%を超えると形成する塗膜の強度が劣下する傾向が認め
られるからである。
In the present invention, polyvinylpyrrolidone having a bond represented by the following formula --CO--N = in the molecule was particularly effective for preventing gelation. Here, the degree of polymerization of the nitrogen-containing vinyl polymer is at most about 200,000, preferably about 100 to 80,000, in consideration of solubility. The composition ratio of the nitrogen-containing vinyl polymer is 0.01 to 50% by mass in the resin component containing the organic binder of the coating composition, preferably
The amount is 0.1 to 10% by mass, more preferably 0.5 to 5% by mass. The composition ratio of the nitrogen-containing vinyl polymer is 0.01% by mass.
If it is less than 50% by weight, the effect of addition and blending is not recognized, and if it exceeds 50% by mass, the strength of the coating film formed tends to be deteriorated.

【0013】本発明に係る塗料組成物において、前記樹
脂成分を溶解する有機溶剤としては、たとえばメチルエ
チルケトン,アセトン,メチルイソブチルケトンなどの
ケトン類、メチルエチルエーテル,ジエチルエーテルな
どのエーテル類、ベンゼン,トルエン,キシレンなどの
芳香族系溶剤、n−ヘキサン,ヘプタンなどの脂肪族系
溶剤、酢酸エチルなどのエステル類、メタノール,エタ
ノール,イソプロピルアルコールなどのアルコール類、
四塩化炭素,トリクロルエチレン,ジクロルエタンなど
のハロゲン系溶剤などの単独、もしくは2種以上の混合
系が挙げられる。 さらに、本発明に係る塗料組成物に
おいては、前記有機バインダー,含窒素ビニル重合体,
および有機溶剤を必須の組成分としているが、必要に応
じて表面調節剤,紫外線吸収剤,増粘剤,染料,顔料,
導電性粉末,金属粉末,劣化防止剤,沈殿防止剤などを
適宜添加してもよい。そして、本発明に係る塗料組成物
の調製に当たっては、たとえば3本ローラ,アトラクタ
ー,ボールミル,サンドミル,ペイントシェーカー,ナ
ノマイザーなどの分散装置を使用し得る。
In the coating composition according to the present invention, examples of the organic solvent for dissolving the resin component include ketones such as methyl ethyl ketone, acetone and methyl isobutyl ketone, ethers such as methyl ethyl ether and diethyl ether, benzene and toluene. , Aromatic solvents such as xylene, aliphatic solvents such as n-hexane and heptane, esters such as ethyl acetate, alcohols such as methanol, ethanol and isopropyl alcohol,
Examples thereof include halogen solvents such as carbon tetrachloride, trichloroethylene, and dichloroethane, or a mixture of two or more kinds. Furthermore, in the coating composition according to the present invention, the organic binder, the nitrogen-containing vinyl polymer,
And the organic solvent is an essential component, but if necessary, a surface regulator, an ultraviolet absorber, a thickener, a dye, a pigment,
Conductive powder, metal powder, deterioration inhibitor, precipitation inhibitor, etc. may be added as appropriate. Then, in preparing the coating composition according to the present invention, a dispersing device such as a three-roller, an attractor, a ball mill, a sand mill, a paint shaker, and a nanomizer can be used.

【0014】本発明に係る塗料組成物は、その用途もし
くは適用分やによっても異なるが、一般的に次ぎのよう
な使用態様が採られる。すなわち、プラスチック類,ゴ
ム類,金属類,もしくはセラミックス類などを素材とし
た構造基材表面を、必要に応じて洗浄処理したり、エッ
チング処理(粗面化)したりし、さらにカップリング剤
やキレート剤などで表面処理を施した後、エアースプレ
ー,エアーレススプレー,静電スプレー,シャワーコー
ト,ディップ塗装,ロール塗装,刷毛塗りなどされる。
Although the coating composition according to the present invention varies depending on its use or application amount, the following use modes are generally adopted. That is, the surface of the structural base material made of plastics, rubbers, metals, ceramics, or the like is subjected to cleaning treatment or etching treatment (roughening) as needed, and further coupling agent or After surface treatment with a chelating agent, etc., air spray, airless spray, electrostatic spray, shower coat, dip coating, roll coating, brush coating, etc.

【0015】特に、前記本発明の塗料組成物を現像装置
の現像ローラ表面層の形成に用いた場合は、前記有機バ
インダとしてフッ素系エラストマーが有効である。ここ
で、フッ素系エラストマーは、トナーなどに対してトナ
ーの固着を生じないため、ウレタンなどを用いた場合に
比べて、現像ローラの寿命が著しく向上する。そして、
このフッ素系エラストマーとしては、たとえばフルオロ
シリコーンゴム,フルオロホスファゼンゴム,ビニリデ
ンフルオライド,ヘキサフルオロプロピレン,ヘキサフ
ルオロプロピレン−テトラフルオロエチレン−ビニリデ
ンフルオライド共重合体,ヘキサフルオロエチレン−テ
トラフルオロエチレン−ビニリデンフルオライド共重合
体などが挙げられる。
Particularly, when the coating composition of the present invention is used for forming the surface layer of the developing roller of the developing device, a fluorine-based elastomer is effective as the organic binder. Here, since the fluorine-based elastomer does not adhere to the toner or the like, the life of the developing roller is remarkably improved as compared with the case where urethane or the like is used. And
Examples of the fluorine-based elastomer include fluorosilicone rubber, fluorophosphazene rubber, vinylidene fluoride, hexafluoropropylene, hexafluoropropylene-tetrafluoroethylene-vinylidene fluoride copolymer, hexafluoroethylene-tetrafluoroethylene-vinylidene fluoride. Examples thereof include copolymers.

【0016】本発明に係る現像装置が具備する現像ロー
ラおよびその製造において、現像ローラ表面(外周面)
に設けられた樹脂層は、前記フッ素系エラストマーを主
成分とし、含窒素ビニル重合体を0.01〜50質量%k範囲
で含む塗料組成物の使用で形成される。具体的には、デ
ィッピング法,スプレー塗布法,ロールコート法などに
よって、現像ローラ基体表面に塗布し、乾燥させること
で形成し得る。なお、前記塗布・乾燥で形成する樹脂層
のまく厚は、さ十分な機械的強度を確保するために、 5
μm 以上、好ましくは30μm 程度以上である。
In the developing roller provided in the developing device according to the present invention and the manufacturing thereof, the developing roller surface (outer peripheral surface)
The resin layer provided in 1 is formed by using a coating composition containing the fluorine-based elastomer as a main component and a nitrogen-containing vinyl polymer in a range of 0.01 to 50 mass% k. Specifically, it can be formed by applying it on the surface of the developing roller substrate by a dipping method, a spray coating method, a roll coating method, or the like and drying it. In addition, the rolling thickness of the resin layer formed by coating and drying is 5% in order to secure sufficient mechanical strength.
It is at least μm, preferably at least about 30 μm.

【0017】[0017]

【作用】本発明に係る塗料組成物においては、主たる塗
膜形成成分を成す有機バインダー(樹脂)の他に、含窒
素ビニル重合体を樹脂成分として含有しており、この含
窒素ビニル重合体によって、その作用は必ずしも明確で
ないが、前記樹脂成分の主体を成している有機バインダ
ーのゲル化が効果的に阻害され、調製後の保存性が大幅
に向上される。そして、この有機バインダーのゲル化阻
害作用は、一様、かつ表面平滑な塗膜の形成を意味し、
良好な外装美観を兼ねた保護膜の形成が可能なことと相
俟って、この種塗料組成物の応用分野の一層の拡大に寄
与するといえる。
The coating composition according to the present invention contains a nitrogen-containing vinyl polymer as a resin component in addition to the organic binder (resin) which constitutes the main coating film forming component. Although its action is not always clear, gelation of the organic binder, which is the main component of the resin component, is effectively inhibited, and the storage stability after preparation is significantly improved. And, the gelation-inhibiting effect of this organic binder means the formation of a uniform and smooth surface coating film,
In combination with the fact that a protective film having a good exterior appearance can be formed, it can be said that this will contribute to further expansion of the application field of this type of coating composition.

【0018】たとえばフッ素系エラストマーは滑らかな
表面を有するので、現像ローラ表面におけるトナーの固
着など容易に防止される。つまり、現像ローラ面は清浄
性を保持し易い状態を採っているため、長期間に亘って
安定した画像を提供することが可能となる。
For example, the fluorine-based elastomer has a smooth surface, so that the adhesion of toner on the surface of the developing roller can be easily prevented. That is, since the developing roller surface is in a state of easily maintaining cleanliness, it is possible to provide a stable image for a long period of time.

【0019】[0019]

【実施例】【Example】

実施例1 先ず、フッ素系エラストマー(有機バインダー)として
のサーモプラスチックT-630(商品名:ダイキン化学kk
製)、ポリビニルピロリドン(含窒素ビニル重合体)、
およびメチルエチルケトン(有機溶剤)を組成分として
用意した。次いで、これらの各組成分を表1に示すよう
な割合(質量比)にそれぞれ秤取し、比較例を含めて5
種類の塗料組成物を調製した。なお、この塗料組成物の
調製は、70℃に加熱保持した状態で、有機溶剤に有機バ
インダーを溶解させた後、さらに含窒素ビニル重合体を
添加し、前記温度に 6時間保持・溶解させることによっ
て行った。
Example 1 First, a thermoplastic T-630 (trade name: Daikin Kagaku kk) as a fluorine-based elastomer (organic binder)
Manufactured), polyvinylpyrrolidone (nitrogen-containing vinyl polymer),
And methyl ethyl ketone (organic solvent) was prepared as a component. Next, each of these compositional components was weighed out in proportions (mass ratios) as shown in Table 1 to obtain 5 including the comparative example.
Various types of coating compositions were prepared. The coating composition should be prepared by dissolving the organic binder in an organic solvent while heating and holding it at 70 ° C, then adding a nitrogen-containing vinyl polymer and holding and dissolving at the temperature for 6 hours. Went by.

【0020】前記調製した直後の塗料組成物の性状(溶
解状態)、および調製後室温に放置したときの、ゲル発
生状態など観察・評価した結果を表1に併せて示した。
比較例bの場合は、沈殿物が認められ形成する塗膜の凹
凸が激しく塗料としての機能がほとんど失われた状態で
あった。
Table 1 also shows the properties (dissolved state) of the coating composition immediately after the preparation and the results of observation and evaluation such as the gel generation state when left at room temperature after the preparation.
In the case of Comparative Example b, a precipitate was recognized and the coating film formed was highly uneven, and the function as a paint was almost lost.

【0021】 表1 実 施 例 比 較 例 A B C a b 有機バインダー 10 10 10 10 10 有機溶剤 120 120 120 120 120 含窒素ビニル重合体 0.1 1 2 0 12 溶解状態 良好 良好 良好 良好 沈殿物 ゲル化時間(hr) 80 1ケ月後ゲル発生無 10 − 上記表1から分かるように、比較例aの塗料組成物が室
温放置10時間後にゲル化が認められたのに対して、実施
例Aの塗料組成物は、80時間経過後にゲル化が認めら
れ、実施例BおよびCの塗料組成物の場合は、1ケ月経
過後でもゲル化の発生が認められず、実施例の場合はい
ずれも保存性(貯蔵性)が向上している。なお、上記実
施例において、フッ素系エラストマー(有機バインダ
ー)の代わりにウレタン系エラストマーもしくはポリア
ミド系エラストマーを、またポリビニルピロリドンの代
わりにポリビニルカルバゾールをそれぞれ用いた他は、
同じ条件で塗料組成物を調製して、調製した直後の塗料
組成物の性状(溶解状態)、および調製後室温に放置し
たときの、ゲル発生状態など観察・評価した結果も同様
であった。
Table 1 Example Comparative Example A B C a b Organic binder 10 10 10 10 10 Organic solvent 120 120 120 120 120 Nitrogen-containing vinyl polymer 0.1 1 2 0 12 Dissolved state Good Good Good Good Precipitate Gelation Time (hr) 80 No gel formation after 1 month 10 − As can be seen from Table 1, the coating composition of Comparative Example a showed gelation after 10 hours of standing at room temperature, whereas the coating composition of Example A The composition showed gelation after 80 hours, and in the case of the coating compositions of Examples B and C, gelation did not occur even after 1 month, and in the case of each of Examples, the preservability was good. (Storability) is improved. In the above examples, urethane elastomer or polyamide elastomer was used instead of the fluorine-based elastomer (organic binder), and polyvinylcarbazole was used instead of polyvinylpyrrolidone.
The coating composition was prepared under the same conditions, and the properties (dissolved state) of the coating composition immediately after preparation and the state of gel generation when the composition was left at room temperature after preparation were also observed and evaluated.

【0022】実施例2 先ず、フッ素系エラストマー(有機バインダー)として
のサーモプラスチックT-630(商品名:ダイキン化学kk
製)、ポリビニルピロリドン(含窒素ビニル重合体)、
メチルエチルケトン(有機溶剤),および導電性カーボ
ン粉末#3050B(商品名:三菱化成kk製)を組成分とし
て用意した。次いで、これらの各組成分を表2に示すよ
うな割合(質量比)にそれぞれ秤取し、比較例を含めて
5種類の塗料組成物を調製した。なお、この塗料組成物
の調製は、70℃に加熱保持した状態で、有機溶剤に有機
バインダーを溶解させた後、さらに含窒素ビニル重合体
を添加し、前記温度に 6時間保持・溶解させてから室温
まで冷却し、この時点で導電性カーボン粉末を加え、ホ
モジナイザーにかけて分散させることによって行った。
Example 2 First, a thermoplastic T-630 (trade name: Daikin Kagaku kk) as a fluoroelastomer (organic binder)
Manufactured), polyvinylpyrrolidone (nitrogen-containing vinyl polymer),
Methyl ethyl ketone (organic solvent) and conductive carbon powder # 3050B (trade name: manufactured by Mitsubishi Kasei kk) were prepared as composition components. Next, each of these composition components was weighed in proportions (mass ratios) shown in Table 2 to prepare five types of coating compositions including comparative examples. The coating composition was prepared by dissolving the organic binder in an organic solvent while heating and holding at 70 ° C., adding a nitrogen-containing vinyl polymer, and holding and dissolving at the temperature for 6 hours. To room temperature, and at this point, conductive carbon powder was added and the mixture was dispersed in a homogenizer.

【0023】前記調製した直後の塗料組成物の性状(溶
解状態)、および調製後室温に放置したときの、ゲル発
生状態など観察・評価した結果を表2に併せて示した。
比較例dの場合は、沈殿物が認められ形成する塗膜の凹
凸が激しく塗料としての機能がほとんど失われた状態で
あった。
Table 2 also shows the properties (dissolved state) of the coating composition immediately after the preparation and the results of observation and evaluation such as the gel generation state when left at room temperature after the preparation.
In the case of Comparative Example d, a precipitate was recognized, and the coating film formed was highly uneven, and the function as a paint was almost lost.

【0024】 表2 実 施 例 比 較 例 D E F c d 有機バインダー 10 10 10 10 10 有機溶剤 120 120 120 120 120 含窒素ビニル重合体 0.1 1 2 0 12 導電性カーボン粉末 1 1 1 1 1 溶解状態 良好 良好 良好 良好 沈殿物 ゲル化時間(hr) 70 1ケ月後ゲル発生無 8 − 上記表1から分かるように、比較例cの塗料組成物が室
温放置 8時間後にゲル化が認められたのに対して、実施
例Dの塗料組成物は、70時間経過後にゲル化が認めら
れ、実施例EおよびFの塗料組成物の場合は、1ケ月経
過後でもゲル化の発生が認められず、実施例の場合はい
ずれも保存性(貯蔵性)が向上している。なお、上記実
施例において、フッ素系エラストマー(有機バインダ
ー)の代わりにウレタン系エラストマーもしくはポリア
ミド系エラストマーを、またポリビニルピロリドンの代
わりにポリビニルカルバゾールをそれぞれ用いた他は、
同じ条件で塗料組成物を調製して、調製した直後の塗料
組成物の性状(溶解状態)、および調製後室温に放置し
たときの、ゲル発生状態など観察・評価した結果も同様
であった。
Table 2 Examples Comparative Example D EF cd Organic binder 10 10 10 10 10 Organic solvent 120 120 120 120 120 Nitrogen-containing vinyl polymer 0.1 1 2 0 12 Conductive carbon powder 1 1 1 1 1 Dissolved Condition Good Good Good Good Precipitate Gelation time (hr) 701 No gel formation after 1 month 8--As can be seen from Table 1 above, gelation was observed after 8 hours at room temperature in the coating composition of Comparative Example c. On the other hand, the coating composition of Example D showed gelation after 70 hours, and the coating compositions of Examples E and F did not show gelation even after 1 month, In each of the examples, the preservability (storability) is improved. In the above examples, urethane elastomer or polyamide elastomer was used instead of the fluorine-based elastomer (organic binder), and polyvinylcarbazole was used instead of polyvinylpyrrolidone.
The coating composition was prepared under the same conditions, and the properties (dissolved state) of the coating composition immediately after preparation and the state of gel generation when the composition was left at room temperature after preparation were also observed and evaluated.

【0025】本発明は、上記実施例に限定されるもので
なく、発明の趣旨を逸脱しない範囲でいろいろの変形を
とり得る。たとえば有機バインダーとして、実施例では
熱可塑性樹脂を一方の樹脂成分としたが、たとえばエポ
キシ系樹脂などの熱硬化性樹脂を一方の樹脂成分とした
場合も、より保存安定性の向上を図り得る。
The present invention is not limited to the above embodiments, but various modifications can be made without departing from the spirit of the invention. For example, as the organic binder, a thermoplastic resin is used as one resin component in the examples, but the storage stability can be further improved even when a thermosetting resin such as an epoxy resin is used as one resin component.

【0026】実施例3 本実施例は現像装置の場合であり、図1および図2を参
照して説明する。
Embodiment 3 This embodiment is for a developing device and will be described with reference to FIGS. 1 and 2.

【0027】図1は現像装置の主要部構成を断面的に示
したもので、1はトナー容器、2は前記トナー容器1内
に収容されたトナー、3はトナー撹拌機、4はトナーを
現像ローラ5に供給するトナー供給ローラである。ま
た、6はスプリング6aによって現像ローラ5外周面に先
端部が押し当てられるトナー層規制部材で、前記現像ロ
ーラ5外周面に担持されるトナー層を制御して、潜像保
持体(感光体ドラム)7面に供給する用に成っている。
さらに、8は帯電器9によって帯電された潜像保持体7
面を露光して、所要の静電潜像を形成する露光器、10は
前記現像ローラ5との接触で、潜像保持体7面のトナー
像(静電潜像の現像)をを記録紙などに転写装置11で転
写後、潜像保持体7面に残存している残留トナーを回収
する一方、潜像保持体7面の清浄化にも寄与するクリー
ニングユニットである。なお、図1において、12はリカ
バリーブレード、13は保護抵抗、14は直流電源で、前記
保護抵抗13を介して現像ローラ5とトナー供給ローラ4
との間にバイバスを印加する。 図2は、前記現像装置
が具備する現像ローラ5の構成を斜視的に示したもの
で,5cはステンレス鋼製のシャフト、5bは前記ステンレ
ス鋼製のシャフト5cの外周面に同心的に配設されたウレ
タン系ゴム層、5aは前記ウレタン系ゴム層5bの外周面に
同心的に配設されたフッ素系エラストマーを主成分と
し、含窒素ビニル重合体を含む膜厚30μm の樹脂層であ
る。すなわち、この樹脂層5aは、前記実施例2で例示し
た塗料組成物E中に、前記ウレタン系ゴム層5bを設けた
現像ローラ基体をジッピングして塗布した後、乾燥機で
20分間乾燥して形成したものである。そして、この現像
ローラ5の表面抵抗は 1×105 Ω・cmであった。
FIG. 1 is a cross-sectional view showing the main structure of the developing device. 1 is a toner container, 2 is toner contained in the toner container 1, 3 is a toner agitator, and 4 is toner developing device. The toner supply roller supplies the roller 5. Reference numeral 6 denotes a toner layer regulating member whose tip end is pressed against the outer peripheral surface of the developing roller 5 by a spring 6a, and controls the toner layer carried on the outer peripheral surface of the developing roller 5 so as to control the latent image holding member (photosensitive drum). ) It is designed to supply 7 sides.
Further, 8 is a latent image holder 7 charged by a charger 9.
An exposure device for exposing a surface to form a desired electrostatic latent image, and 10 is a contact sheet with the developing roller 5 to form a toner image (development of the electrostatic latent image) on the surface of the latent image carrier 7 on a recording sheet. This is a cleaning unit that collects the residual toner remaining on the surface of the latent image holding member 7 after the transfer by the transfer device 11 to the above, and also contributes to cleaning of the surface of the latent image holding member 7. In FIG. 1, 12 is a recovery blade, 13 is a protective resistor, 14 is a DC power source, and the developing roller 5 and the toner supply roller 4 are connected via the protective resistor 13.
Bypass is applied between and. FIG. 2 is a perspective view showing the structure of the developing roller 5 included in the developing device. 5c is a stainless steel shaft, and 5b is concentrically arranged on the outer peripheral surface of the stainless steel shaft 5c. The urethane rubber layer 5a is a resin layer having a film thickness of 30 μm, which is mainly composed of a fluorine elastomer and is concentrically arranged on the outer peripheral surface of the urethane rubber layer 5b and contains a nitrogen-containing vinyl polymer. That is, this resin layer 5a was applied to the coating composition E exemplified in Example 2 by zipping the developing roller base body provided with the urethane rubber layer 5b and then applying it with a drier.
It was formed by drying for 20 minutes. The surface resistance of the developing roller 5 was 1 × 10 5 Ω · cm.

【0028】上記現像装置を下記条件に設定し画出しを
行った。
Image development was carried out by setting the above developing device under the following conditions.

【0029】トナー(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 2重量部,外添剤シリカ 0.5
重量部から成る堆積平均粒径10μm の非磁性一成分系ト
ナーを用いた。また、潜像保持体(感光体ドラム)7の
回転を50mm/ sと設定し、帯電器9からのコロナ放電
で、潜像保持体7面を一様な表面電位(+500V)に帯電
する。その後、露光機8としてのレーザ光で画像情報を
潜像保持体7面に記録(潜像形成)してから、表面速度
100mm/ sで回転させ、かつ+200Vを印加した現像ロー
ラ5を潜像保持体7面に押し当て現像を行った。この現
像されたトナー像を転写装置11で記録紙に転写した後、
熱定着した。
As the toner (developer) 2, 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, 0.5 parts of silica as an external additive.
A non-magnetic one-component toner having a deposition average particle size of 10 μm composed of parts by weight was used. Further, the rotation of the latent image carrier (photosensitive drum) 7 is set to 50 mm / s, and the surface of the latent image carrier 7 is charged to a uniform surface potential (+500 V) by corona discharge from the charger 9. After that, after the image information is recorded (latent image formation) on the surface of the latent image holder 7 by the laser beam as the exposure device 8, the surface speed is changed.
The developing roller 5 rotated at 100 mm / s and applied with +200 V was pressed against the surface of the latent image holding member 7 for development. After transferring the developed toner image onto the recording paper by the transfer device 11,
Heat fixed.

【0030】前記転写後の画像は,ライン画像が鮮明
で、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。
In the image after the transfer, the line image was clear and the solid image was a uniform and high-density image. Also, 5
The 10,000 images after the life test were also clear images with no deterioration and maintaining the initial state. Furthermore, extremely good images were obtained even under high temperature and high humidity conditions.

【0031】[0031]

【発明の効果】以上説明したように、本発明に係る塗料
組成物によれば、有機バインダー成分のフッ素系エラス
トマーが有機溶剤に比較的溶解し難い場合でも、沈殿の
発生やゲル状化の発生が抑制、もしくは防止されて、保
存性が大幅に改善向上される。たとえば、耐候性や耐汚
染性など注目される特性を有しながら、各種の有機溶剤
に難溶解性であるため、塗膜としての利用が難しかった
フッ素系エラストマーの塗料化を容易に成し得ることに
な。つまり、本発明に係る塗料組成物の溶解性改善、も
しくは溶液保存性の向上・改善によって、フッ素系エラ
ストマー成分の特長を、より有効に利用した実用的な保
護塗膜の形成が可能となる。
As described above, according to the coating composition of the present invention, even when the fluoroelastomer as the organic binder component is relatively difficult to dissolve in the organic solvent, precipitation or gelation occurs. Is suppressed or prevented, and storability is significantly improved. For example, it is possible to easily form a fluoroelastomer paint that has been difficult to use as a coating film because it has poor properties such as weather resistance and stain resistance but is hardly soluble in various organic solvents. Especially In other words, by improving the solubility of the coating composition according to the present invention, or improving / improving the storability of the solution, it becomes possible to form a practical protective coating film that more effectively utilizes the characteristics of the fluoroelastomer component.

【0032】また、このような塗料組成物を、現像装置
の現像ローラ表面樹脂層形成に用いることにより、現像
ローラにすぐれた耐候性,耐汚染性を付与し得るので、
長期間に亘って安定した画像を形成し得る現像装置の提
供が可能である。
Further, by using such a coating composition for forming the resin layer on the surface of the developing roller of the developing device, excellent weather resistance and stain resistance can be imparted to the developing roller.
It is possible to provide a developing device capable of forming a stable image for a long period of time.

【図面の簡単な説明】[Brief description of drawings]

【図1】本発明に係る現像装置の要部構成例を示す断面
図。
FIG. 1 is a sectional view showing a configuration example of a main part of a developing device according to the present invention.

【図2】本発明に係る現像装置が具備する現像ローラの
要部構成例を示す斜視図。
FIG. 2 is a perspective view showing a configuration example of a main part of a developing roller included in the developing device according to the present invention.

【符号の説明】[Explanation of symbols]

5……現像ローラ 5a……フッ素系エラストマーを主成分とし含窒素ビニル
重合体を含む樹脂層 5b……ウレタン系ゴム層 5c……ステンレス鋼製のシャフト
5 ... Development roller 5a ... Resin layer 5b containing fluorine-based elastomer as a main component and containing nitrogen-containing vinyl polymer ... Urethane-based rubber layer 5c ... Stainless steel shaft

フロントページの続き (72)発明者 真常 泰 神奈川県川崎市幸区小向東芝町1番地 株式会社東芝 研究開発センター内 (72)発明者 大杉 之弘 静岡県三島市南町6−78 株式会社テッ ク技術研究所内 (56)参考文献 特開 平6−282101(JP,A) 特開 平4−204677(JP,A) 特開 昭60−151823(JP,A) 特開 昭58−68230(JP,A) 特開 平7−72721(JP,A) 特開 平1−108270(JP,A) (58)調査した分野(Int.Cl.7,DB名) C09D 5/00 - 201/10 C08L 39/06 G03G 9/087 G06G 15/06 G03G 15/08 Front page continuation (72) Inventor, Yasushi Masatsugu Komukai Toshiba Town, Saiwai-ku, Kawasaki City, Kanagawa Prefecture, Toshiba Research & Development Center Co., Ltd. (56) Reference JP-A-6-282101 (JP, A) JP-A-4-204677 (JP, A) JP-A-60-151823 (JP, A) JP-A-58-68230 (JP , A) JP-A-7-72721 (JP, A) JP-A-1-108270 (JP, A) (58) Fields investigated (Int.Cl. 7 , DB name) C09D 5/00-201/10 C08L 39/06 G03G 9/087 G06G 15/06 G03G 15/08

Claims (3)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 フッ素系エラストマーを主成分とし、
リビニルピロリドンを含む樹脂成分と有機溶剤成分とを
組成分として調製された塗料組成物であって、 前記樹脂成分の0.01〜50質量%をポリビニルピロ
リドンが占めていることを特徴とする塗料組成物。
1. A fluorine-based elastomer as a main component, Po
A coating composition prepared a resin component and an organic solvent component as component comprising polyvinyl pyrrolidone, Poribinirupiro 0.01 to 50% by weight of the resin component
A coating composition characterized by being occupied by redone .
【請求項2】 潜像保持体と、この潜像保持体に対向し
て配設された現像ローラとを具備する現像装置におい
て、 前記現像ローラ基体表面にフッ素系エラストマーを主成
分とし、ポリビニルピロリドンを0.01〜50質量%
の範囲で含む樹脂層を設けたことを特徴とする現像装
置。
2. A developing device comprising a latent image holding member and a developing roller which is disposed so as to face the latent image holding member, wherein the surface of the developing roller base is made of a fluoroelastomer as a main component, and polyvinylpyrrolidone is used. 0.01 to 50% by mass
The developing device is characterized in that a resin layer is included in the range.
【請求項3】 潜像保持体と、この潜像保持体に対向し
て配設された現像ローラとを具備する現像装置の製造方
法において、前記現像ローラ基体表面にフッ素系エラス
トマーを主成分とし、ポリビニルピロリドンを0.01
〜50質量%の範囲で含有する樹脂成分および有機溶剤
を組成分とする塗料組成物を塗布、乾燥することを特徴
とする現像装置の製造方法。
3. A latent image bearing member, in the manufacturing method of the developing apparatus comprising a developing roller which is disposed to face the latent image holding member, a fluorine-based Elastica on the developing roller substrate surface
Toma as the main component and polyvinylpyrrolidone 0.01
A method for producing a developing device, which comprises applying a coating composition containing a resin component and an organic solvent contained in an amount of ˜50% by mass, and drying the coating composition.
JP05412095A 1995-03-14 1995-03-14 Paint composition, developing device, and method of manufacturing developing device Expired - Fee Related JP3403848B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP05412095A JP3403848B2 (en) 1995-03-14 1995-03-14 Paint composition, developing device, and method of manufacturing developing device

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP05412095A JP3403848B2 (en) 1995-03-14 1995-03-14 Paint composition, developing device, and method of manufacturing developing device

Publications (2)

Publication Number Publication Date
JPH08245925A JPH08245925A (en) 1996-09-24
JP3403848B2 true JP3403848B2 (en) 2003-05-06

Family

ID=12961749

Family Applications (1)

Application Number Title Priority Date Filing Date
JP05412095A Expired - Fee Related JP3403848B2 (en) 1995-03-14 1995-03-14 Paint composition, developing device, and method of manufacturing developing device

Country Status (1)

Country Link
JP (1) JP3403848B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013245314A (en) * 2012-05-28 2013-12-09 Noda Screen:Kk Coating agent

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3136982A1 (en) * 1981-09-17 1983-03-31 Basf Ag, 6700 Ludwigshafen MAGNETIC RECORDING CARRIER
JPS60151823A (en) * 1984-01-20 1985-08-09 Victor Co Of Japan Ltd Magnetic recording medium
JPH0830164B2 (en) * 1987-10-20 1996-03-27 旭硝子株式会社 Paint composition
JP2878835B2 (en) * 1990-11-30 1999-04-05 株式会社東芝 Charging member
JPH06282101A (en) * 1993-03-25 1994-10-07 Toshiba Corp Method and device for developing
JPH0772721A (en) * 1993-06-29 1995-03-17 Mitsubishi Chem Corp Conductive controlling member

Also Published As

Publication number Publication date
JPH08245925A (en) 1996-09-24

Similar Documents

Publication Publication Date Title
JPS61163366A (en) Image maintaining member
JP4221949B2 (en) Toner carrier
JP3403848B2 (en) Paint composition, developing device, and method of manufacturing developing device
JPS58117555A (en) Carrier for electrophotographic dry type developer
JP3112489B2 (en) Developing device
JPS598821B2 (en) Magnetic toner for developing electrostatic images
US6341420B1 (en) Method of manufacturing a developer roller
JP2853598B2 (en) Surface-treated cleaning blade, surface treatment method thereof, and image forming method
JP2858005B2 (en) Development method
JPS6223308B2 (en)
JPH09146345A (en) Electrostatic charging roll and image forming device
JPH03192377A (en) Developing device
US5627001A (en) Coated carrier particle containing a charge control agent
JP2003345070A (en) Electrophotographic carrier, developer and image forming method
US5659862A (en) Developer roll for electrophotographic copiers and printers, and process for manufacturing it by powder coating
JP2569581B2 (en) Carrier for developer
JPH021881A (en) Developing method for electrostatic latent image
JP2728749B2 (en) Developing device
JP2002014534A (en) Developing roller and developing device
JPH04204677A (en) Charging member
JP2569582B2 (en) Carrier for developer
JPH04188160A (en) Electrophotographic carrier
EP1439923A1 (en) Method of manufacturing a developer roller
JP2002311630A (en) Base for electrophotographic planographic printing plate
JPH02108081A (en) Developing device by one-component toner

Legal Events

Date Code Title Description
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20030212

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20080229

Year of fee payment: 5

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090228

Year of fee payment: 6

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100228

Year of fee payment: 7

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100228

Year of fee payment: 7

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110228

Year of fee payment: 8

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120229

Year of fee payment: 9

LAPS Cancellation because of no payment of annual fees