JPH11231571A - Nonmagnetic one-component developing toner - Google Patents
Nonmagnetic one-component developing tonerInfo
- Publication number
- JPH11231571A JPH11231571A JP4429998A JP4429998A JPH11231571A JP H11231571 A JPH11231571 A JP H11231571A JP 4429998 A JP4429998 A JP 4429998A JP 4429998 A JP4429998 A JP 4429998A JP H11231571 A JPH11231571 A JP H11231571A
- Authority
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- Prior art keywords
- toner
- silica
- weight
- amount
- chargeable silica
- 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.)
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Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、複写機またはプリ
ンターなどの画像出力装置に使用するトナーに関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a toner used in an image output device such as a copying machine or a printer.
【0002】[0002]
【従来の技術】非磁性1成分現像方法は、トナーと搬送
部材の静電気力によってトナーを搬送部材表面に担持し
て現像位置まで搬送し、感光体表面の潜像を現像するも
のである。トナーと搬送部材間に静電気力を発生させる
ためには、搬送部材と当接した層厚規制部材を使用する
ことが多く、該層厚規制部材と搬送部材の間をトナーが
通過する時に、トナーは帯電することになる。また、ト
ナーを瞬時に均一に帯電させるためには、トナーを薄層
化することが重要となり、該部材はトナー層の規制も同
時に行うことになる。それ故搬送部材及び層厚規制部材
が、トナーに汚染されると搬送部材上のトナーを所望の
帯電量に制御できなくなり、カブリ増加や白スジ状の濃
度ムラが発生することになる。2. Description of the Related Art In a non-magnetic one-component developing method, toner is carried on a conveying member surface by an electrostatic force of toner and a conveying member, is conveyed to a developing position, and develops a latent image on a photoreceptor surface. In order to generate an electrostatic force between the toner and the conveying member, a layer thickness regulating member in contact with the conveying member is often used, and when the toner passes between the layer thickness regulating member and the conveying member, the toner Will be charged. In order to charge the toner instantaneously and uniformly, it is important to make the toner thinner, and the member also controls the toner layer at the same time. Therefore, if the conveying member and the layer thickness regulating member are contaminated with the toner, the toner on the conveying member cannot be controlled to a desired charge amount, which causes an increase in fog and density unevenness such as white stripes.
【0003】従来、トナー汚染を軽減するために、外添
シリカの増量が提案されている。これはトナーが搬送部
材と層厚規制部材との間を通過する際に生じる摩擦熱に
よるトナー成分の融着を防止することを目的としている
が、充分にトナー汚染を防止することができない。Hitherto, to reduce toner contamination, an increase in the amount of external silica has been proposed. This is intended to prevent fusion of toner components due to frictional heat generated when the toner passes between the conveying member and the layer thickness regulating member, but it cannot sufficiently prevent toner contamination.
【0004】[0004]
【発明が解決しようとする課題】本発明の目的は、搬送
部材及び層厚規制部材へのトナー汚染がなく、繰り返し
使用しても高画質な画像を提供できる負帯電性非磁性1
成分現像用トナーを提供する。SUMMARY OF THE INVENTION It is an object of the present invention to provide a negatively-chargeable non-magnetic material which can provide a high-quality image even when used repeatedly without causing toner contamination on a conveying member and a layer thickness regulating member.
Provided is a toner for component development.
【0005】[0005]
【課題を解決するための手段】本発明は非磁性1成分現
像用トナーを担持して搬送する搬送部材と、該搬送部材
に圧接して設けられた層厚規制部材とを少なくとも有す
る現像装置に使用するトナーであって、該トナーは、結
着樹脂、着色剤、負帯電性電荷制御剤を必須成分とする
樹脂粉末の表面に、少なくとも疎水化処理された正帯電
性シリカ及び負帯電性シリカを付着させることにより、
搬送部材及び層厚規制部材へのトナー融着が防止される
こと。また該正帯電性シリカと該負帯電性シリカの添加
量をそれぞれWpとWn、及びこれらの飽和帯電量の絶
対値を|Qp|と|Qn|としたとき、下記(1)式を
満足するシリカ外添方法とすることにより、搬送部材、
層厚規制部材にトナー融着がなく、且つ高画像濃度でカ
ブリの少ない画像が得られることを見出した。According to the present invention, there is provided a developing apparatus having at least a conveying member for carrying and conveying a non-magnetic one-component developing toner and a layer thickness regulating member provided in pressure contact with the conveying member. A toner to be used, wherein the toner is a binder resin, a colorant, a surface of a resin powder containing a negatively chargeable charge controlling agent as essential components, at least a hydrophobically treated positively chargeable silica and a negatively chargeable silica. By attaching
To prevent toner fusion to the conveying member and the layer thickness regulating member. Further, when the addition amounts of the positively chargeable silica and the negatively chargeable silica are Wp and Wn, and the absolute values of the saturated charge amounts thereof are | Qp | and | Qn |, the following expression (1) is satisfied. By adopting a silica external addition method, a conveying member,
It has been found that an image having high image density and less fog can be obtained without toner fusion to the layer thickness regulating member.
【0006】[0006]
【数2】 (Equation 2)
【0007】[0007]
【発明の実施の形態】以下、本発明を詳細に説明する。
本発明のトナーに使用される結着樹脂としては、アルコ
ール成分例えばジアルコール成分、多価アルコール成分
とカルボン酸成分例えばジカルボン酸成分、多価カルボ
ン酸成分とから得られたポリエステル樹脂、又は一部に
ウレタン結合を有するポリエステル樹脂などのポリエス
テル樹脂、あるいはスチレンアクリル共重合体などの従
来非磁性1成分トナー用結着剤として公知の熱可塑性樹
脂が使用される。これらの結着樹脂は、トナーの保存安
定性の面から、ガラス転移点が55℃以上の結着樹脂で
あることが好ましく、その酸価は40以下であることが
好ましい。酸価が40を超えると耐湿性が劣化し好まし
くない。さらに好ましくは20以下である。DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described below in detail.
As the binder resin used in the toner of the present invention, an alcohol component such as a dialcohol component, a polyester resin obtained from a polyhydric alcohol component and a carboxylic acid component such as a dicarboxylic acid component, a polycarboxylic acid component, or a part thereof A polyester resin such as a polyester resin having a urethane bond, or a thermoplastic resin known as a binder for a conventional non-magnetic one-component toner such as a styrene acrylic copolymer is used. From the viewpoint of storage stability of the toner, these binder resins are preferably binder resins having a glass transition point of 55 ° C. or higher, and preferably have an acid value of 40 or lower. If the acid value exceeds 40, the moisture resistance deteriorates, which is not preferable. More preferably, it is 20 or less.
【0008】本発明のトナーに使用される着色剤として
は、トナーに従来使用されてきた任意の適当な顔料また
は染料が挙げられる。顔料としてはカーボンブラック、
アニリンブラック、アセチレンブラック、ナフトールイ
エロー、ハンザイエロー、ローダミンレーキ、アリザリ
ンレーキ、ベンガラ、フタロシアニンブルー、インダン
スレンブルー等が例示される。これらの顔料は定着画像
の光学濃度を維持するのに必要充分な量が用いられ、通
常結着樹脂100重量部に対し0.1〜20重量部、好
ましくは0.2〜10重量部添加される。染料として、
アゾ系染料、アントラキノン系染料、キサンテン系染
料、メチン系染料等が例示される。これらの染料は通常
結着樹脂100重量部に対し0.1〜20重量部、好ま
しくは0.3〜10重量部添加される。[0008] Colorants used in the toner of the present invention include any suitable pigments or dyes conventionally used in toners. Pigments such as carbon black,
Examples include aniline black, acetylene black, naphthol yellow, hansa yellow, rhodamine lake, alizarin lake, red bengala, phthalocyanine blue, and indanthrene blue. These pigments are used in an amount necessary and sufficient to maintain the optical density of the fixed image, and are usually added in an amount of 0.1 to 20 parts by weight, preferably 0.2 to 10 parts by weight, based on 100 parts by weight of the binder resin. You. As a dye,
Examples include azo dyes, anthraquinone dyes, xanthene dyes, methine dyes, and the like. These dyes are generally added in an amount of 0.1 to 20 parts by weight, preferably 0.3 to 10 parts by weight, based on 100 parts by weight of the binder resin.
【0009】負帯電性電荷制御剤としては、例えば有機
金属錯体やキレート化合物が有効であり、アゾ系金属錯
体、アセチルアセトン金属錯体、芳香族ハイドロキシカ
ルボン酸、芳香族ダイカルボン酸、芳香族モノ及びポリ
カルボン酸及びその金属塩、無水物、エステル類、ビス
フェノール等のフェノール誘導体類などが挙げられる。
これらの電荷制御剤は通常結着樹脂100重量部に対し
0.1〜10重量部、好ましくは0.5〜5重量部の範
囲で配合される。上記範囲の上限を超えると帯電不良が
生じてカブリ等による画像品質の低下が起こり、下限未
満であると十分な帯電量が得られず、画像濃度の低下、
多数枚連続コピーしたときに画像濃度が安定しないとい
う問題が生ずる。また樹脂粉末にはポリプロピレンワッ
クスやポリエチレンワックス等の離型剤等を含有させて
もよい。As the negatively chargeable charge controlling agent, for example, an organic metal complex or a chelate compound is effective. An azo-based metal complex, an acetylacetone metal complex, an aromatic hydroxycarboxylic acid, an aromatic dicarboxylic acid, an aromatic mono- and poly-organic complex are preferable. Examples thereof include carboxylic acids and metal salts thereof, anhydrides, esters, and phenol derivatives such as bisphenol.
These charge control agents are generally added in an amount of 0.1 to 10 parts by weight, preferably 0.5 to 5 parts by weight, based on 100 parts by weight of the binder resin. Exceeding the upper limit of the above range causes poor charging and causes deterioration in image quality due to fogging and the like, and a charge amount less than the lower limit does not provide a sufficient charge amount, lowering the image density,
There is a problem that the image density is not stable when a large number of continuous copies are made. The resin powder may contain a release agent such as polypropylene wax or polyethylene wax.
【0010】樹脂粉末は前記結着樹脂、着色剤、負帯電
性電荷制御剤等を溶融混練、粉砕、分級して得てもよい
し、結着樹脂の重合時に着色剤、負帯電性電荷制御剤等
を含有させて得る重合法で得てもよい。樹脂粉末の表面
に下記で述べる正帯電性シリカ及び負帯電性シリカを付
着させるには、ヘンシェルミキサーやスーパーミキサー
等の攪拌機で付着させればよく、正帯電性シリカ及び負
帯電性シリカは樹脂粉末の表面にまぶしと呼ばれる弱い
状態で付着されていてもよいし、正帯電性シリカ及び負
帯電性シリカの一部が樹脂粉末の内部に埋没し固着され
ている状態でもよい。樹脂粒子の表面には正帯電性シリ
カ及び負帯電性シリカの他にアルミナ、チタニア、酸化
亜鉛等の無機酸化物、カーボンブラック等の導電性微粒
子等が付着されていてもよい。The resin powder may be obtained by melt-kneading, pulverizing and classifying the binder resin, the colorant, the negative charge control agent, and the like, or the colorant, the negative charge control and the like during polymerization of the binder resin. It may be obtained by a polymerization method containing an agent or the like. In order to attach the positively chargeable silica and the negatively chargeable silica described below to the surface of the resin powder, it is sufficient to attach the positively chargeable silica and the negatively chargeable silica using a stirrer such as a Henschel mixer or a super mixer. May be attached to the surface of the resin powder in a weak state called a glare, or a state in which a part of the positively chargeable silica and the negatively chargeable silica is buried and fixed inside the resin powder. In addition to the positively chargeable silica and the negatively chargeable silica, inorganic fine particles such as alumina, titania, and zinc oxide, and conductive fine particles such as carbon black may be attached to the surface of the resin particles.
【0011】本発明に使用される疎水化された負帯電性
シリカ及び正帯電性シリカとしては、市販のものも使用
できるが、飽和帯電量とトナー表面への付着量の関係式
である(1)式を満足するようなシリカを選定し、その
量を決めることが高画像濃度でカブリの少ない画像を得
るために必要である。(1)式の中央項の値Wn×|Q
n|/Wp×|Qp|が7より小さい場合には、カブリ
が増加し、30より大きい場合には搬送部材(以下、ス
リーブという)や層厚規制部材(以下、ブレードとい
う)にトナーが融着しやすい。また、正帯電性シリカの
添加量は樹脂粉末100重量部に対して0.025重量
部より多くすることが必要で、0.025重量部より少
ない場合ではトナー融着防止効果が認められない。上限
は負帯電性シリカの添加量と飽和帯電量とから(1)式
から求められる。負帯電性シリカの添加量はトナーの流
動性などを考慮して決めれば良いが0.02〜1重量部
が好ましく、更に0.5〜0.9重量部が好ましい。As the hydrophobicized negatively chargeable silica and positively chargeable silica used in the present invention, commercially available ones can be used, but the relational expression between the saturated charge amount and the amount of adhesion to the toner surface is given by (1). It is necessary to select silica that satisfies the expression and determine its amount in order to obtain an image with high image density and less fog. (1) Value of central term Wn × | Q
When n | / Wp × | Qp | is smaller than 7, fog increases, and when n | / Wp × | Qp | is larger than 30, the toner is fused to a conveying member (hereinafter, referred to as a sleeve) or a layer thickness regulating member (hereinafter, referred to as a blade). Easy to wear. Further, the amount of the positively chargeable silica needs to be more than 0.025 parts by weight with respect to 100 parts by weight of the resin powder, and if it is less than 0.025 parts by weight, the effect of preventing fusion of the toner is not recognized. The upper limit is determined from the formula (1) from the amount of the negatively chargeable silica and the amount of the saturated charge. The amount of the negatively chargeable silica may be determined in consideration of the fluidity of the toner, but is preferably 0.02 to 1 part by weight, more preferably 0.5 to 0.9 part by weight.
【0012】負帯電性シリカと正帯電性シリカを本発明
の範囲にて併用した場合に、トナー融着が生じない理由
は完全に解明されてはいないが、スリーブとブレードの
帯電極性はトナーの正規帯電極性(本発明の場合は負帯
電)とは逆極性に位置するため、負帯電性シリカのみを
付着させたトナーではブレードやスリーブに強固に付着
しやすくなり、トナーがブレードとスリーブ間を通過す
る時の摩擦力が増大し、結果的にトナー融着が生じると
考えられる。The reason why toner fusion does not occur when negatively chargeable silica and positively chargeable silica are used together within the scope of the present invention has not been completely elucidated. Since the polarity is opposite to the normal charge polarity (negative charge in the case of the present invention), the toner to which only the negatively chargeable silica is attached easily adheres firmly to the blade or the sleeve. It is considered that the frictional force at the time of passing increases, and as a result, toner fusion occurs.
【0013】しかるに、本発明の範囲にて正帯電性シリ
カを添加すると、トナー表面の一部にニュートラル乃至
正極性に帯電する部分が生じ、しかもこの部分がコロ作
用を発揮することで、トナーに与えられる上記摩擦力が
弱まり、結果的にトナー融着が防止され、且つ極端な正
帯電量の発生もないためにカブリや濃度ウス、トナー飛
散を生じにくいトナーになると考えられる。However, if the positively chargeable silica is added within the scope of the present invention, a portion of the toner surface that is neutrally charged or positively charged is formed, and this portion exerts a roller action, so that the toner is The applied frictional force is weakened. As a result, it is considered that the toner is prevented from fusing, and since there is no generation of an extremely large positive charge amount, the toner is unlikely to cause fog, density loss, and toner scattering.
【0014】負帯電性シリカとしては、親水性シリカを
ヘキサメチレンジシラザン、ジメチルジクロロシランな
どのシラン化合物、ジメチルシリコーンオイル、各種変
性シリコーンオイルなどにより疎水化処理した公知のも
のが使用可能である。正帯電性シリカとしては、親水性
シリカをアミノ変性シリコーンオイル、第4級アンモニ
ウム化合物など、またはこれら正極性処理剤とともに各
種シラン化合物により疎水化及び正帯電性付与処理を行
った公知のものが使用可能である。As the negatively chargeable silica, known silica obtained by subjecting hydrophilic silica to a hydrophobic treatment with a silane compound such as hexamethylenedisilazane or dimethyldichlorosilane, dimethylsilicone oil, or various modified silicone oils can be used. As the positively chargeable silica, use is made of known silica obtained by subjecting hydrophilic silica to an amino-modified silicone oil, a quaternary ammonium compound, or the like, or performing a hydrophobic treatment and a positive charge imparting treatment with various silane compounds together with these positive treatment agents. It is possible.
【0015】該正帯電性及び負帯電性シリカの一次平均
径はおおよそ10〜50nmのものがトナー流動性付与
効果が高く好ましく使用でき、疎水性の尺度としてのメ
タノールウェッタビリティー値が40以上が好ましい。
更に好ましくは45以上である。40を下回ると高温環
境でのトナー帯電の低下が大きくなり好ましくない。The positively chargeable and negatively chargeable silica having an average primary particle diameter of about 10 to 50 nm is preferably used because of its high toner fluidity-providing effect, and has a methanol wettability value of at least 40 as a measure of hydrophobicity. preferable.
More preferably, it is 45 or more. If it is less than 40, the toner charging in a high-temperature environment is undesirably reduced.
【0016】正帯電性シリカと負帯電性シリカの最適な
合計添加量は、トナーの粒子径分布やシリカ添加前の樹
脂粉末の流動性などにより一概には決められないが、例
えば体積平均径8〜9μmのトナーであれば、樹脂粉末
100重量部に対して0.2〜2重量部が好ましい。更
に好ましくは0.4〜1.5重量部である。2重量部を
越えると環境安定性や定着性の低下を伴いやすく好まし
くない。The optimum total addition amount of the positively chargeable silica and the negatively chargeable silica cannot be unconditionally determined by the particle size distribution of the toner or the fluidity of the resin powder before silica addition. In the case of a toner having a size of 9 μm, the amount is preferably 0.2 to 2 parts by weight based on 100 parts by weight of the resin powder. More preferably, it is 0.4 to 1.5 parts by weight. If it exceeds 2 parts by weight, environmental stability and fixability tend to decrease, which is not preferable.
【0017】該正帯電性及び負帯電性シリカの飽和帯電
量Qpμc/g及びQnμc/gの測定方法を説明す
る。正帯電性又は負帯電性シリカを150メッシュ篩い
にて篩い分けして150メッシュをパスしたシリカを測
定に使用する。キャリア(パウダーテック社製:FSL
1020)99.8gと測定用シリカ0.2gを150
ccのポリビンに入れ、22〜24℃/57〜62%R
Hに調整された雰囲気に10時間放置する。その後、定
回転の回転装置に該ポリビンを設置した後この雰囲気下
でポリビンを回転させ混合撹拌を行う。混合過程におい
て、シリカの帯電量をブローオフ帯電量測定機にて初期
より5分おきに3回ずつ測定し、3回の平均値を整数一
位を四捨五入してその撹拌時間における帯電量とする。
シリカの帯電量は時系列上ある時点で最大となり、それ
以後は低下するので該撹拌混合過程における最大帯電量
を本発明でいう飽和帯電量とする。ブローオフ帯電量測
定機において測定する際キャリアとシリカの分離に使用
するステンレス製の網には400メッシュのものを使用
する。A method for measuring the saturated charge amounts Qpμc / g and Qnμc / g of the positively and negatively chargeable silica will be described. The positively or negatively chargeable silica is sieved with a 150 mesh sieve, and the silica that has passed 150 mesh is used for the measurement. Carrier (Powdertech: FSL)
1020) 99.8 g and 0.2 g of silica for measurement are added to 150
22-24 ° C / 57-62% R
Leave for 10 hours in an atmosphere adjusted to H. Thereafter, the polybin is set on a rotating device of constant rotation, and then the polybin is rotated under this atmosphere to perform mixing and stirring. In the mixing process, the charge amount of the silica is measured three times every five minutes from the beginning by a blow-off charge amount measuring device, and the average value of the three times is rounded to the nearest whole number to obtain the charge amount during the stirring time. .
Since the charge amount of silica becomes maximum at a certain point in time series and thereafter decreases, the maximum charge amount in the stirring and mixing process is defined as the saturated charge amount in the present invention. A 400 mesh mesh is used as a stainless steel net used for separating the carrier and silica when measuring with a blow-off charge amount measuring device.
【0018】[0018]
【実施例】以下に実施例を示すが、本発明は何等これら
に限定されるものではない。The present invention will be described in more detail with reference to the following Examples, but it should not be construed that the invention is limited thereto.
【0019】 <樹脂粉末Aの製造> ポリエステル樹脂(Tg=63℃、Mn=3900、Mw=48300、 THF不溶分=13%) 100 重量部 カーボンブラック(キャボット社製:リーガル400R) 5.5重量部 負帯電性電荷制御剤(オリエント化学社製:S−34) 1.3重量部 ポリプロピレンワックス 1.5重量部 (三洋化成工業社製:ビスコール550P) 上記材料を均一に混合した後、押し出し機にて充分混練
した。冷却後に粉砕分級を行い、体積平均径9.5μm
の樹脂粉末Aを得た。<Production of Resin Powder A> Polyester resin (Tg = 63 ° C., Mn = 3900, Mw = 48300, THF insoluble content = 13%) 100 parts by weight Carbon black (Cabot Corporation: Regal 400R) 5.5 parts by weight Part Negatively chargeable charge control agent (Orient Chemical Co., Ltd .: S-34) 1.3 parts by weight Polypropylene wax 1.5 parts by weight (Sanyo Chemical Industries Co., Ltd .: Viscol 550P) After uniformly mixing the above materials, an extruder And kneaded well. After cooling, pulverization and classification were performed, and the volume average diameter was 9.5 μm.
Resin powder A was obtained.
【0020】 <負帯電性疎水性シリカの例> 1.シリカA (メタノールウェッタビリティー値=48、 ジメチルジクロロシラン処理、比表面積110m2 /g) 飽和帯電量Qn=−320μc/g 2.シリカB (メタノールウェッタビリティー値=80、 ヘキサメチレンジシラザン処理、比表面積140m2 /g) 飽和帯電量Qn=−490μc/g<Example of Negatively Chargeable Hydrophobic Silica> Silica A (methanol wettability value = 48, dimethyldichlorosilane treatment, specific surface area 110 m 2 / g) Saturated charge amount Qn = −320 μc / g Silica B (methanol wettability value = 80, hexamethylene disilazane treatment, specific surface area 140 m 2 / g) Saturated charge amount Qn = −490 μc / g
【0021】 <正帯電性疎水性シリカの例> 飽和帯電量Qp 1.シリカC(クラリアントジャパン社製:HVK2115 ) +130μc/g 2.シリカD(クラリアントジャパン社製:H3050EP ) +380μc/g 上記樹脂粉末Aに表1に示すようにシリカをヘンシェル
ミキサーで付着させ実施例及び比較例トナーを作製し市
販の非磁性1成分現像プリンタ(20PPM)にてプリ
ントテストを行い、画像濃度(ID)、カブリ(B
G)、トナー融着の有無を確認した。テスト環境条件は
22〜25℃/55〜65%RHである。プリントテス
トは印字率約6%の文字チャートを繰り返しプリントし
た。トナー融着の有無は、ハーフトーン画像(A4サイ
ズ)をプリントすることにより確認した。その実写テス
トの結果は表2に示すとおりである。なお、画像濃度
(ID)はベタ画像をマクベスRD−914にて測定し
た反射濃度であり、カブリ(BG)はプリント前の用紙
とプリント後の同用紙における非画像部のハンター白色
度の差を示す。<Example of Positively Chargeable Hydrophobic Silica> Saturated charge amount Qp Silica C (manufactured by Clariant Japan: HVK2115) +130 μc / g Silica D (manufactured by Clariant Japan Co., Ltd .: H3050EP) +380 μc / g Silica is adhered to the resin powder A by a Henschel mixer as shown in Table 1 to prepare toners of Examples and Comparative Examples. ), A print test is performed, and image density (ID), fog (B
G), the presence or absence of toner fusion was confirmed. The test environment conditions are 22-25 ° C./55-65% RH. In the print test, a character chart having a printing rate of about 6% was repeatedly printed. The presence or absence of toner fusion was confirmed by printing a halftone image (A4 size). The results of the actual test are shown in Table 2. The image density (ID) is the reflection density of a solid image measured by Macbeth RD-914, and the fog (BG) is the difference in hunter whiteness of the non-image portion between the paper before printing and the same paper after printing. Show.
【0022】[0022]
【表1】 [Table 1]
【0023】[0023]
【表2】 [Table 2]
【0024】[0024]
【発明の効果】上記の比較検討の結果から明らかなよう
に、本発明のトナーは結着樹脂、着色剤、負帯電性電荷
制御剤を必須成分とする樹脂粉末の表面に、疎水化処理
された正負の帯電性シリカが付着していることにより好
ましい帯電量を得ることができ、特に7≦Wn×|Qn
|/Wp×|Qp|≦30の間になるようにした一成分
現像用トナーは実写テストでも7000枚後に於ても、
スリーブへのトナーの付着が認められず好適であった。As is apparent from the results of the above comparative study, the toner of the present invention is subjected to a hydrophobic treatment on the surface of a resin powder containing a binder resin, a colorant and a negatively chargeable charge control agent as essential components. A favorable charge amount can be obtained by the addition of the positive and negative chargeable silica, and in particular, 7 ≦ Wn × | Qn
| / Wp × | Qp | ≦ 30, the one-component developing toner can be used in both the actual printing test and after 7000 sheets.
The toner was not adhering to the sleeve and was suitable.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 宮本 篤生 静岡県静岡市用宗巴町3番1号 株式会社 巴川製紙所化成品事業部内 ────────────────────────────────────────────────── ─── Continuing on the front page (72) Inventor Atsushi Miyamoto 3-1 Yomoe Tomoecho, Shizuoka City, Shizuoka Pref.
Claims (2)
を必須成分とする樹脂粉末の表面に、少なくとも疎水化
処理された正帯電性シリカ及び疎水化処理された負帯電
性シリカが付着してなり、前記樹脂粉末100重量部に
対して正帯電性シリカの付着量をWp重量部及び飽和帯
電量をQpμc/g、負帯電性シリカの付着量をWn重
量部及び飽和帯電量をQnμc/gとしたとき、下記
(1)式を満足することを特徴とする非磁性1成分現像
用トナー。 【数1】 1. A surface of a resin powder containing a binder resin, a colorant and a negatively chargeable charge controlling agent as essential components, at least a positively chargeable silica subjected to a hydrophobic treatment and a negatively chargeable silica subjected to a hydrophobic treatment. With respect to 100 parts by weight of the resin powder, the amount of the positively chargeable silica is Wp part by weight and the amount of the saturated charge is Qpμc / g, and the amount of the negatively chargeable silica is Wn part by weight and the amount of the saturated charge is 100 parts by weight. A toner for non-magnetic one-component development, which satisfies the following expression (1) when Qnμc / g is satisfied. (Equation 1)
タノールウェッタビリティー値が40以上であることを
特徴とする請求項1記載の非磁性1成分現像用トナー。2. The non-magnetic one-component developing toner according to claim 1, wherein the methanol wettability of the positively chargeable silica and the negatively chargeable silica is 40 or more.
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JP04429998A JP3383765B2 (en) | 1998-02-12 | 1998-02-12 | Non-magnetic one-component developing toner |
Applications Claiming Priority (1)
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---|---|---|---|
JP04429998A JP3383765B2 (en) | 1998-02-12 | 1998-02-12 | Non-magnetic one-component developing toner |
Publications (2)
Publication Number | Publication Date |
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JPH11231571A true JPH11231571A (en) | 1999-08-27 |
JP3383765B2 JP3383765B2 (en) | 2003-03-04 |
Family
ID=12687636
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JP04429998A Expired - Fee Related JP3383765B2 (en) | 1998-02-12 | 1998-02-12 | Non-magnetic one-component developing toner |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6994942B2 (en) | 2001-07-11 | 2006-02-07 | Seiko Epson Corporation | Non-magnetic single-component toner, method of preparing the same, and image forming apparatus using the same |
US7217486B2 (en) | 2003-01-17 | 2007-05-15 | Seiko Epson Corporation | Toner and image-forming apparatus using the toner |
US10248036B2 (en) | 2017-03-24 | 2019-04-02 | Kyocera Document Solutions Inc. | Positively chargeable toner |
US10768542B2 (en) | 2018-05-15 | 2020-09-08 | Kyocera Document Solutions Inc. | Positively chargeable toner |
-
1998
- 1998-02-12 JP JP04429998A patent/JP3383765B2/en not_active Expired - Fee Related
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6994942B2 (en) | 2001-07-11 | 2006-02-07 | Seiko Epson Corporation | Non-magnetic single-component toner, method of preparing the same, and image forming apparatus using the same |
US7217486B2 (en) | 2003-01-17 | 2007-05-15 | Seiko Epson Corporation | Toner and image-forming apparatus using the toner |
US10248036B2 (en) | 2017-03-24 | 2019-04-02 | Kyocera Document Solutions Inc. | Positively chargeable toner |
US10768542B2 (en) | 2018-05-15 | 2020-09-08 | Kyocera Document Solutions Inc. | Positively chargeable toner |
Also Published As
Publication number | Publication date |
---|---|
JP3383765B2 (en) | 2003-03-04 |
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