JPH08254852A - Electrophotographic toner - Google Patents
Electrophotographic tonerInfo
- Publication number
- JPH08254852A JPH08254852A JP7059434A JP5943495A JPH08254852A JP H08254852 A JPH08254852 A JP H08254852A JP 7059434 A JP7059434 A JP 7059434A JP 5943495 A JP5943495 A JP 5943495A JP H08254852 A JPH08254852 A JP H08254852A
- Authority
- JP
- Japan
- Prior art keywords
- toner
- charge
- binder resin
- permittivity
- loss
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 229920005989 resin Polymers 0.000 claims abstract description 29
- 239000011347 resin Substances 0.000 claims abstract description 29
- 239000011230 binding agent Substances 0.000 claims abstract description 26
- 239000004645 polyester resin Substances 0.000 claims description 16
- 229920001225 polyester resin Polymers 0.000 claims description 16
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 7
- 229910052799 carbon Inorganic materials 0.000 claims description 7
- 239000000470 constituent Substances 0.000 claims description 3
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 abstract description 13
- 239000002245 particle Substances 0.000 description 16
- 238000004898 kneading Methods 0.000 description 11
- 238000012360 testing method Methods 0.000 description 10
- 238000009825 accumulation Methods 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 229920006395 saturated elastomer Polymers 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical group [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 239000012212 insulator Substances 0.000 description 3
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 230000000630 rising effect Effects 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 1
- 235000002597 Solanum melongena Nutrition 0.000 description 1
- 244000061458 Solanum melongena Species 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229910021417 amorphous silicon Inorganic materials 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- -1 ferrite Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 238000012800 visualization Methods 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Landscapes
- Developing Agents For Electrophotography (AREA)
Abstract
(57)【要約】
【目的】 少ない帯電制御剤の使用で、帯電立ち上りの
速度が大きい電子写真用トナーを提供すること。
【構成】 バインダ樹脂の損失誘電率に対するトナーの
損失誘電率の比を1.2〜2.3の範囲にする。(57) [Abstract] [Purpose] To provide an electrophotographic toner having a high rate of rise in charge by using a small amount of a charge control agent. [Constitution] The ratio of the loss permittivity of the toner to the loss permittivity of the binder resin is set in the range of 1.2 to 2.3.
Description
【0001】[0001]
【産業上の利用分野】本発明は、電子写真法等において
静電潜像を現像するために用いるトナーに関する。さら
に詳しくは、トナーの帯電速度の向上に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a toner used for developing an electrostatic latent image in electrophotography or the like. More specifically, it relates to improvement of the charging speed of toner.
【0002】[0002]
【従来の技術】電子写真法は、光導電性絶縁体(フォト
コンドラムなど)に、コロナ放電などにより一様な静電
荷を与え、様々な手段により該光導電性絶縁体上に光像
を照射することによって静電潜像を形成する。ここに、
トナーと呼ばれる微粉末を帯電させ、帯電したトナーが
電気的吸引力により潜像に付着することによって現像、
可視化を行い、必要に応じて紙等にトナー画像を転写し
た後、加圧、加熱、光等の照射などの手段により紙等の
記録媒体上にトナー画像を定着させて複写物を得るもの
である。2. Description of the Related Art In electrophotography, a photoconductive insulator (such as a photocondrum) is provided with a uniform electrostatic charge by corona discharge or the like, and an optical image is formed on the photoconductive insulator by various means. Irradiation forms an electrostatic latent image. here,
Develop by charging fine powder called toner, and the charged toner adheres to the latent image by electric attraction.
Visualization is performed, and the toner image is transferred to paper or the like as needed, and then the toner image is fixed on a recording medium such as paper by a means such as pressurization, heating, or irradiation with light to obtain a copy. is there.
【0003】トナーは従来より、天然または合成高分子
物質よりなるバインダ樹脂、カーボンブラックあるいは
染料等の着色および帯電制御の役割を担う物質、さらに
はワックス類等が、単独あるいは複数組み合わせて用い
られ、これらをバインダ樹脂中に分散させたものを5〜
20μm程度に微粉砕した粒子が用いられている。静電
潜像を現像するためのトナーは、鉄粉、マグネタイト、
フェライト等の鉄あるいは金属酸化物、または前記物質
に種々のコートを施した担体物質(キャリア)と混合さ
れることにより、摩擦帯電させられる(二成分現像方
法)。また、トナー単体で用いる場合、該トナーを現像
装置の壁面や現像装置内のマグネットロールなどの部材
と摩擦することにより摩擦帯電させる(一成分現像方
法)。Conventionally, a toner is made of a binder resin made of a natural or synthetic polymer substance, a substance such as carbon black or a dye, which plays a role of controlling coloring and charge, and waxes, alone or in combination. 5 to 5 of these dispersed in a binder resin
Particles finely pulverized to about 20 μm are used. Toner for developing an electrostatic latent image is iron powder, magnetite,
By mixing with iron or metal oxide such as ferrite, or a carrier substance (carrier) obtained by applying various coatings to the above substances, they are triboelectrically charged (two-component developing method). When the toner is used alone, it is frictionally charged by rubbing the toner against a wall surface of the developing device or a member such as a magnet roll in the developing device (one-component developing method).
【0004】電子写真において高速、大量の印刷を行っ
た場合、大量のトナーが消費されるため、供給したトナ
ーを速やかに印刷可能な帯電量まで上昇させなければな
らない。光定着の代表的なものであるフラッシュ定着
は、非接触定着であるため、現像時の画像の解像度を
劣化させない。電源投入後の待ち時間がなく、クイッ
クスタートが可能である。システムダウンにより定着
器内に記録紙が詰まっても発火しない。のり付き紙、
プレプリント紙、厚さの異なる紙など、記録紙の材質や
厚さに関係なく定着可能である。等の特徴を持ち、高
速、大量の印刷に用いられる。このようなプリンタにお
いては、特に、トナーの帯電を速やかに行う必要があ
る。When a large amount of toner is printed at high speed in electrophotography, a large amount of toner is consumed. Therefore, the supplied toner must be quickly raised to a printable charge amount. Since flash fixing, which is a typical optical fixing, is non-contact fixing, it does not deteriorate the resolution of an image during development. There is no waiting time after the power is turned on, and quick start is possible. Even if the recording paper is jammed in the fixing device due to system down, it does not ignite. Glued paper,
It can be fixed regardless of the material and thickness of the recording paper, such as preprinted paper or paper with different thickness. It has features such as, and is used for high-speed, large-volume printing. In such a printer, it is especially necessary to quickly charge the toner.
【0005】[0005]
【発明が解決しようとする課題】トナーの飽和帯電量お
よび帯電上昇速度はトナーの構成要素、すなわち、バイ
ンダ樹脂、カーボン、染料等の帯電制御剤のバランスで
決まる。帯電制御剤の量を増加させれば、帯電速度およ
び飽和帯電量を高くすることはできるが、帯電制御剤は
高価であり、大量の使用は控えたい。また、多量の使用
はトナーの他の特性に悪影響を及ぼす可能性がある。従
来、小量の帯電制御剤、あるいは同一量の帯電制御剤の
使用において、帯電上昇速度を高くする方法の検討はな
されていなかった。The saturated charge amount and charge rising speed of the toner are determined by the balance of the constituent elements of the toner, that is, the charge control agent such as the binder resin, carbon and dye. The charge rate and the saturated charge amount can be increased by increasing the amount of the charge control agent, but the charge control agent is expensive and it is not desirable to use it in a large amount. Also, the use of large amounts can adversely affect other properties of the toner. Heretofore, there has been no study on a method for increasing the rate of charge increase when a small amount of charge control agent or the same amount of charge control agent is used.
【0006】本発明は、前記のような事情を鑑みてなさ
れたもので、少ない帯電制御剤の使用で、帯電立ち上が
りの速度が大きい電子写真用トナーを提供することを目
的とする。The present invention has been made in view of the above circumstances, and it is an object of the present invention to provide an electrophotographic toner having a high charge rising speed by using a small amount of a charge control agent.
【0007】[0007]
【課題を解決するための手段】トナーの帯電は発生する
電荷の蓄積と漏洩のバランスで決まることが知られてお
り、これに従った比電荷の経時変化の式が公知となって
いる(下記文献1,2)。 〔文献1〕唐木田健一:電子写真学会第60回研究討論
会、p.1,(1987) 〔文献2〕松井乃里恵、岡孝造:電子写真学会誌、p.
307、第27巻、第3号(1988) 電荷の発生はキャリアなどの担持体(二成分現像)、ブ
レード等のプリンタ部材(一成分現像)とトナーの摩擦
によって起こり、電荷の漏洩の度合いが変化しなけれ
ば、単位時間の電荷の蓄積速度が高いほど、帯電の上昇
速度も大きくなると考えられる。また、電荷の漏洩は、
担持体、またはプリンタ部材を通してアース、あるいは
空気中に向かって起こると考えられ、電荷の蓄積の度合
いが変化しなければ、電荷の漏洩が大きくなると、飽和
帯電量に到達する時間が早く、すなわち、帯電の上昇速
度が大きくなり、飽和帯電量が小さくなる傾向があるこ
とが予測される。It is known that the charging of toner is determined by the balance between the accumulation and leakage of generated charges, and an equation for the change of specific charge with time according to this is known (see below). References 1 and 2). [Reference 1] Kenichi Karakida: The 60th Research Forum of the Electrophotographic Society, p. 1, (1987) [Reference 2] Norie Matsui, Kozo Oka: Journal of Electrophotographic Society, p.
307, Vol. 27, No. 3 (1988) The electric charge is generated by friction between a carrier such as a carrier (two-component development), a printer member such as a blade (one-component development) and the toner, and the degree of charge leakage varies. If it does not change, it is considered that the higher the rate of charge accumulation per unit time, the higher the rate of increase in charging. In addition, the leakage of charge is
It is thought that it occurs toward the ground through the carrier or the printer member, or into the air, and if the degree of charge accumulation does not change, the greater the leakage of charge, the faster the time to reach the saturated charge amount, that is, It is predicted that the rate of increase in charge tends to increase and the saturated charge amount tends to decrease.
【0008】実際には、電荷の蓄積と漏洩の一方を固定
し、他方のみ変えることは難しく、双方のバランスで決
まるとしか言えない場合が多いのであるが、電荷の蓄
積、および漏洩が支配していることは確実である。トナ
ーは絶縁体領域の高い抵抗率を持つ、すなわち、誘電体
である。そして、その特性を示す誘電率の実数部分(貯
蔵誘電率、ε’)、および虚数部分(損失誘電率、
ε'') はそれぞれ、電荷の蓄積と漏洩に関係を持つこと
が予想される。したがって、誘電特性は、トナーの帯電
速度に関係を持つ可能性が大きい。In practice, it is difficult to fix one of the charge accumulation and the leakage and to change only the other, and in many cases it can be said that it is determined only by the balance between the two. However, the charge accumulation and the leakage dominate. Is certain. Toner has a high resistivity in the insulator region, ie it is a dielectric. Then, the real number part (storage permittivity, ε ') and the imaginary number part (loss permittivity,
Each ε '') is expected to be related to charge accumulation and leakage. Therefore, the dielectric property is likely to be related to the charging speed of the toner.
【0009】発明者らは、検討の結果、トナーの損失誘
電率(ε'') がトナーの帯電速度と相関を示し、損失誘
電率が大きいほど帯電速度も大きくなることを見いだ
し、本発明をなすに至った。他の誘電特性、貯蔵誘電率
(ε’)および誘電正接(tan δ)は帯電速度と明
確な相関を持たない。As a result of studies, the inventors have found that the loss permittivity (ε ″) of the toner has a correlation with the charging rate of the toner, and that the higher the loss permittivity, the higher the charging rate. It came to eggplant. Other dielectric properties, storage permittivity (ε ′) and dissipation factor (tan δ) have no clear correlation with the charging rate.
【0010】損失誘電率は導電率に相当する量である。
発明者らの検討によれば、トナーの損失誘電率は、重量
分率の大半を占めるバインダ樹脂の値をベースとし、そ
の他の成分が入ることにより増加する。したがって、バ
インダ樹脂が変われば、ベースの値も変わるので、損失
誘電率の絶対値で帯電速度との関係を決定することはで
きない。帯電速度との関係は、ベース値からの変化量あ
るいは変化量比により決定されていることがわかる。検
討の結果、トナーの損失誘電率がバインダ樹脂の損失誘
電率に対し、1.2以上あれば、十分な帯電速度を持つ
ことがわかった。損失誘電率比が2.3を越えると、帯
電速度が大きいが、飽和帯電量が適正範囲を越えてしま
う。また、摩擦に従って、徐々に帯電量が上昇する傾向
を示し、電子写真における使用に適しない。The loss permittivity is an amount corresponding to conductivity.
According to the studies by the inventors, the loss permittivity of the toner is increased based on the value of the binder resin, which accounts for the majority of the weight fraction, and the inclusion of other components. Therefore, if the binder resin changes, the value of the base also changes, so the relationship with the charging speed cannot be determined by the absolute value of the loss permittivity. It can be seen that the relationship with the charging rate is determined by the amount of change from the base value or the change ratio. As a result of the examination, it was found that the toner has a sufficient charging rate if the loss permittivity of the toner is 1.2 or more with respect to the loss permittivity of the binder resin. When the loss permittivity ratio exceeds 2.3, the charging speed is high, but the saturated charge amount exceeds the proper range. In addition, the amount of charge tends to gradually increase with friction and is not suitable for use in electrophotography.
【0011】電子写真用トナーの損失誘電率およびバイ
ンダ樹脂の損失誘電率を調整する手段は一概ではなく、
経験的、実験的にならざるを得ない。バインダ樹脂の損
失誘電率は樹脂の種類とその製法などに応じて決まる。
トナーの損失誘電率はバインダ樹脂中に含まれる電荷調
整剤などの種類、量にもよるが、実際の使用量は少ない
ので、量よりも他の条件、この場合、導電性成分の分散
状態が重要な因子と考えられる。これはトナーの製造
(混練)条件によって変化する。具体的には、ニーダの
回転数が高くなると、損失誘電率の値も上昇する傾向が
あるように見える。ただし、分散状態は温度によっても
変化するため、常に成立する関係とは言いがたい。トナ
ーの損失誘電率は、カーボンおよび染料のトナー中の分
散状態に影響を受けている。分散状態は、ニーダの回転
シェアが樹脂を通して、カーボン、染料にどのように伝
わるかによって決定されている。これは樹脂粘度によっ
て変化し、低粘度においては、ニーダ回転数に関わら
ず、シェアが伝わらないことがある。しかし、高粘度状
態でも、回転数を上げすぎると、歯の近傍のみ高シェア
であるが、少し離れた位置においてはほとんどシェアが
かからない場合もある。Means for adjusting the loss permittivity of the electrophotographic toner and the loss permittivity of the binder resin are not unconditional.
It has to be empirical and experimental. The loss permittivity of the binder resin is determined according to the type of resin and its manufacturing method.
The loss dielectric constant of the toner depends on the type and amount of the charge control agent contained in the binder resin, but the actual amount used is small, so other conditions than this amount, in this case, the dispersion state of the conductive component It is considered to be an important factor. This changes depending on the toner manufacturing (kneading) conditions. Specifically, it seems that the value of the loss permittivity tends to increase as the kneader rotation speed increases. However, the dispersed state changes with temperature, so it cannot be said that the relationship always holds. The loss dielectric constant of a toner is affected by the dispersion state of carbon and dye in the toner. The dispersion state is determined by how the rotational shear of the kneader is transmitted to the carbon and the dye through the resin. This changes depending on the resin viscosity, and at low viscosity, the shear may not be transmitted regardless of the kneader rotation speed. However, even in a high-viscosity state, if the number of revolutions is increased too much, the high share is achieved only in the vicinity of the teeth, but there is a case where little share is applied at a position slightly apart.
【0012】このように損失誘電率比を調製することに
より、トナー中の電荷調整剤の量を従来の典型的な例と
比較して50%程度減らすことができる。本発明で用い
るトナーバインダ、カーボン、着色剤、帯電制御剤、ワ
ックス類などは電子写真に通常用いられる、公知の材料
を使用することができる。トナーバインダ樹脂として
は、ポリエステル樹脂、エポキシ樹脂などを用いること
ができる。フラッシュ定着方式では、トナーの速やかな
融解と用紙への浸透が要求され、これらの要求を満たす
樹脂として、好ましくはポリエステル樹脂が使用され
る。By adjusting the loss permittivity ratio in this way, the amount of the charge control agent in the toner can be reduced by about 50% as compared with the conventional typical example. As the toner binder, carbon, colorant, charge control agent, waxes and the like used in the present invention, known materials usually used in electrophotography can be used. As the toner binder resin, polyester resin, epoxy resin or the like can be used. In the flash fixing method, prompt melting of toner and penetration into paper are required, and a polyester resin is preferably used as a resin satisfying these requirements.
【0013】高速印刷においては、感光体としてアモル
ファスシリコンが使用される場合が多く、この場合、ト
ナーを正帯電とする必要がある。ポリエステル樹脂は、
負帯電性である場合が多いので、ニグロシン系、第4級
アンモニウム塩系等の帯電制御剤を使用して正帯電とす
る。もともと負帯電性のものを正帯電にすると、帯電制
御剤の添加の量、状態等により、帯電量が低かったり、
立ち上がりが遅くなることが多く、帯電の立ち上がりに
ついての考慮が必須となる。In high-speed printing, amorphous silicon is often used as a photoconductor, and in this case, the toner needs to be positively charged. Polyester resin
Since it is often negatively charged, it is positively charged by using a charge control agent such as a nigrosine type or a quaternary ammonium salt type. If a negative charge is originally charged positively, the charge amount may be low, depending on the amount and condition of the charge control agent added.
It often takes a long time to start up, and it is necessary to consider the rise of charging.
【0014】本発明で用いるトナーは、従来公知の方法
で製造できる。すなわち、バインダ樹脂、着色剤、およ
び要すればカーボン、帯電制御剤などを、例えば、加圧
ニーダ、ロールミル、エクストルーダなどにより溶融混
練して均一に分散し、例えば、ジェットミルなどによ
り、微粉砕化し、分級機、例えば、風力分級機などによ
り分級して所望のトナーを得ることができる。さらに必
要であれば、製造したトナーに、例えば、シリカ粉、フ
ッ素樹脂粉、酸化チタン微粉等を外添剤として添加する
こともできる。The toner used in the present invention can be manufactured by a conventionally known method. That is, a binder resin, a colorant, and optionally carbon, a charge control agent, etc. are melt-kneaded by, for example, a pressure kneader, a roll mill, an extruder, etc. and uniformly dispersed, and for example, finely pulverized by, for example, a jet mill. A desired toner can be obtained by classification with a classifier such as an air classifier. Further, if necessary, silica powder, fluororesin powder, titanium oxide fine powder, or the like can be added as an external additive to the manufactured toner.
【0015】[0015]
【実施例】以下、実施例により本発明をさらに具体的に
説明するが、本発明はこれによって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 the present invention is not limited thereto.
【0016】〔実施例1〕バインダ樹脂として、ポリエ
ステル樹脂(1)(ダイヤクロンER−501、三菱レ
ーヨン製)92重量部に対し、着色材としてカーボンブ
ラック(モガールL、キャボット製)5重量部、ニグロ
シン系染料(オイルブラックBY、オリエント化学製)
3重量部を加え、加圧ニーダにより140℃,100r.
p.m.で30分溶融混練し、トナー塊を得た。冷却したト
ナー塊をロートプレックス粉砕機により粒径約2mmの粗
粉トナーとした。次いで、該トナーをジェットミルを用
いて微粉砕を行い、粉砕物を風力分級機により分級し、
粒径5〜20μmの正帯電トナーAを得た。Example 1 As a binder resin, 5 parts by weight of carbon black (Mogal L, made by Cabot) as a coloring material to 92 parts by weight of polyester resin (1) (Diacron ER-501, made by Mitsubishi Rayon), Nigrosine dye (Oil Black BY, Orient Chemical)
Add 3 parts by weight, and press a kneader to 140 ° C, 100r.
Melt kneading was performed for 30 minutes at pm to obtain a toner mass. The cooled toner lump was made into a coarse powder toner having a particle diameter of about 2 mm by a Rotoplex pulverizer. Then, the toner is finely pulverized using a jet mill, and the pulverized product is classified by an air classifier,
A positively charged toner A having a particle size of 5 to 20 μm was obtained.
【0017】トナーAの誘電特性は、以下の様にして求
めた。トナー粉体を450kg重/cm 2 にて圧縮、タブレ
ットに成形(KBr錠剤成形器、ハンドプレス:SSP
−10A、島津製作所製)した後、誘電体損測定装置
(TR−10C、WBG−9、BDA−9、SE−4
3、TO−10、安藤電気製)を用いて、印加電圧20
V、周波数1000Hzで測定し、貯蔵誘電率(ε’)、
損失誘電率(ε'') および誘電損失(tan δ)を求
めた。The dielectric properties of Toner A are determined as follows.
I have 450 kg weight of toner powder / cm 2Compressed at
Molding (KBr tablet molding machine, hand press: SSP
-10A, manufactured by Shimadzu Corporation), and then dielectric loss measuring device
(TR-10C, WBG-9, BDA-9, SE-4
3, TO-10, manufactured by Ando Electric Co., Ltd., and applied voltage 20
V, frequency 1000 Hz, storage permittivity (ε '),
Calculate loss permittivity (ε '') and dielectric loss (tan δ)
I have
【0018】帯電速度および飽和帯電量は以下の様にし
て求めた。ポリビン中に、Aトナー6重量部、マグネタ
イトキャリア(関東電化工業製)94重量部を取り、ボ
ールミルにて攪拌、適当な時間ごとにサンプリングし、
ブローオフ法により帯電量を求めた(TB−100、東
芝ケミカル製)。これをグラフにプロットし、前記文献
2に記載の下記式によりカーブフィットを行い、帯電の
立ち上がりの時定数τを求めた。The charging speed and the saturated charge amount were determined as follows. 6 parts by weight of A toner and 94 parts by weight of magnetite carrier (manufactured by Kanto Denka Kogyo Co., Ltd.) were placed in a polybin, stirred by a ball mill, and sampled at appropriate intervals
The charge amount was determined by the blow-off method (TB-100, manufactured by Toshiba Chemical). This was plotted on a graph, and a curve fit was performed by the following formula described in the above-mentioned Document 2 to obtain a time constant τ of rising of charging.
【0019】 qmax −q=(qmax −qo )exp(−t/τ) 式中、q:トナーの帯電量 t:混合時間 τ:帯電上昇の時定数 qmax :t=0の時のq qo :t=∞の時のq Aトナー6重量部、マグネタイトキャリア(関東電化工
業製)94重量部を取り、現像剤を調製し、FACOM
−6700レーザプリンタ改造機を用いて印刷試験を行
った。Q max −q = (q max −q o ) exp (−t / τ) where q: toner charge amount t: mixing time τ: time constant of charge rise q max : when t = 0 Q q o : When t = ∞, 6 parts by weight of the qA toner and 94 parts by weight of magnetite carrier (manufactured by Kanto Denka Kogyo Co., Ltd.) are taken to prepare a developer, and FACOM is used.
A printing test was conducted using a modified 6700 laser printer.
【0020】〔実施例2〕バインダ樹脂として、ポリエ
ステル樹脂(1)を用い、混練の条件を140℃,20
0r.p.m.で30分とし、実施例1と同様にして、粒径5
〜20μmの正帯電トナーBを得た後、誘電率および帯
電の時定数を求め、印刷試験を行った。Example 2 A polyester resin (1) was used as a binder resin, and the kneading conditions were 140 ° C. and 20 ° C.
It was set to 0 rpm for 30 minutes, and the particle size was 5 in the same manner as in Example 1.
After obtaining a positively charged toner B having a particle size of up to 20 μm, the dielectric constant and the charging time constant were determined and a printing test was conducted.
【0021】〔実施例3〕バインダ樹脂として、ポリエ
ステル樹脂(1)を用い、混練の条件を130℃,20
0r.p.m.で30分とし、実施例1と同様にして、粒径5
〜20μmの正帯電トナーCを得た後、誘電率および帯
電の時定数を求め、印刷試験を行った。Example 3 A polyester resin (1) was used as a binder resin, and the kneading conditions were 130 ° C. and 20 ° C.
It was set to 0 rpm for 30 minutes, and the particle size was 5 in the same manner as in Example 1.
After obtaining a positively charged toner C having a particle size of up to 20 μm, the dielectric constant and the charging time constant were determined and a printing test was conducted.
【0022】〔実施例4〕バインダ樹脂として、ポリエ
ステル樹脂(2)(プライオトン5120、グッドイヤ
ー製)を用い、混練の条件を140℃,100r.p.m.で
30分とし、実施例1と同様にして、粒径5〜20μm
の正帯電トナーDを得た後、誘電率および帯電の時定数
を求め、印刷試験を行った。Example 4 Polyester resin (2) (Pryoton 5120, manufactured by Goodyear) was used as a binder resin, and the kneading conditions were 140 ° C. and 100 rpm for 30 minutes. Particle size 5 to 20 μm
After obtaining the positively charged toner D, the dielectric constant and the charging time constant were determined, and a printing test was performed.
【0023】〔実施例5〕バインダ樹脂として、ポリエ
ステル樹脂(2)を用い、混練の条件を140℃,20
0r.p.m.で30分とし、実施例1と同様にして、粒径5
〜20μmの正帯電トナーEを得た後、誘電率および帯
電の時定数を求め、印刷試験を行った。Example 5 A polyester resin (2) was used as a binder resin, and the kneading conditions were 140 ° C. and 20 ° C.
It was set to 0 rpm for 30 minutes, and the particle size was 5 in the same manner as in Example 1.
After obtaining the positively charged toner E having a particle size of up to 20 μm, the dielectric constant and the charging time constant were determined and a printing test was conducted.
【0024】〔実施例6〕バインダ樹脂として、ポリエ
ステル樹脂(2)を用い、混練の条件を130℃,20
0r.p.m.で30分とし、実施例1と同様にして、粒径5
〜20μmの正帯電トナーFを得た後、誘電率および帯
電の時定数を求め、印刷試験を行った。Example 6 A polyester resin (2) was used as a binder resin, and the kneading conditions were 130 ° C. and 20 ° C.
It was set to 0 rpm for 30 minutes, and the particle size was 5 in the same manner as in Example 1.
After obtaining a positively charged toner F having a particle size of up to 20 μm, the dielectric constant and the charging time constant were determined and a printing test was conducted.
【0025】〔比較例1〕バインダ樹脂として、ポリエ
ステル樹脂(1)を用い、混練の条件を130℃,50
r.p.m.で30分とし、実施例1と同様にして、粒径5〜
20μmの正帯電トナーGを得た後、誘電率および帯電
の時定数を求め、印刷試験を行った。Comparative Example 1 Polyester resin (1) was used as the binder resin, and the kneading conditions were 130 ° C. and 50
The rpm was set to 30 minutes, and the particle size was 5 to 5 in the same manner as in Example 1.
After obtaining the positively charged toner G of 20 μm, the dielectric constant and the charging time constant were determined and a printing test was conducted.
【0026】〔比較例2〕バインダ樹脂として、ポリエ
ステル樹脂(1)を用い、混練の条件を140℃,30
0r.p.m.で30分とし、実施例1と同様にして、粒径5
〜20μmの正帯電トナーHを得た後、誘電率および帯
電の時定数を求め、印刷試験を行った。[Comparative Example 2] Polyester resin (1) was used as the binder resin, and the kneading conditions were 140 ° C and 30 ° C.
It was set to 0 rpm for 30 minutes, and the particle size was 5 in the same manner as in Example 1.
After obtaining a positively charged toner H of ˜20 μm, the dielectric constant and the charging time constant were determined and a printing test was conducted.
【0027】〔比較例3〕バインダ樹脂として、ポリエ
ステル樹脂(2)を用い、混練の条件を130℃,50
r.p.m.で30分とし、実施例1と同様にして、粒径5〜
20μmの正帯電トナーIを得た後、誘電率および帯電
の時定数を求め、印刷試験を行った。[Comparative Example 3] Polyester resin (2) was used as the binder resin, and the kneading conditions were 130 ° C and 50 ° C.
The rpm was set to 30 minutes, and the particle size was 5 to 5 in the same manner as in Example 1.
After obtaining the positively charged toner I of 20 μm, the dielectric constant and the time constant of charging were obtained and a printing test was conducted.
【0028】〔比較例4〕バインダ樹脂として、ポリエ
ステル樹脂(2)を用い、混練の条件を140℃,30
0r.p.m.で30分とし、実施例1と同様にして、粒径5
〜20μmの正帯電トナーJを得た後、誘電率および帯
電の時定数を求め、印刷試験を行った。上記実施例およ
び比較例の結果を表1と図1,2に示した。損失誘電率
の比が1.2以下では、帯電不足によるカブリが発生
し、2.3以上では40分を経過すると帯電量の上昇に
より、印刷物の光学密度の低下が見られた。損失誘電率
の比が1.2〜2.3の範囲では、良好な印字が得られ
る。[Comparative Example 4] Polyester resin (2) was used as a binder resin, and the kneading conditions were 140 ° C and 30 ° C.
It was set to 0 rpm for 30 minutes, and the particle size was 5 in the same manner as in Example 1.
After obtaining a positively charged toner J of ˜20 μm, the dielectric constant and the charging time constant were determined and a printing test was conducted. The results of the above Examples and Comparative Examples are shown in Table 1 and FIGS. When the ratio of loss permittivity was 1.2 or less, fog occurred due to insufficient charging, and when 2.3 or more, after 40 minutes, the charge amount increased and the optical density of the printed matter decreased. If the ratio of loss permittivity is in the range of 1.2 to 2.3, good printing can be obtained.
【0029】[0029]
【表1】 [Table 1]
【図1】実施例におけるトナーとポリエステル樹脂
(1)の誘電率比と帯電上昇の時定数の関係を示す。FIG. 1 shows the relationship between the dielectric constant ratio of toner and polyester resin (1) and the time constant of charge increase in Examples.
【図2】実施例におけるトナーとポリエステル樹脂
(2)の誘電率比と帯電上昇の時定数の関係を示す。FIG. 2 shows the relationship between the dielectric constant ratio of toner and polyester resin (2) and the time constant of charge increase in Examples.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 内藤 浩昭 兵庫県加東郡社町佐保35番(番地なし) 富士通周辺機株式会社内 (72)発明者 田邨 ひろみ 神奈川県川崎市中原区上小田中1015番地 富士通株式会社内 (72)発明者 猿渡 紀男 神奈川県川崎市中原区上小田中1015番地 富士通株式会社内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Hiroaki Naito No.35 Saho, Shrine-cho, Kato-gun, Hyogo Prefecture (No address) Inside Fujitsu Peripheral Machinery Co., Ltd. Address within Fujitsu Limited (72) Inventor Norio Saruwatari 1015 Kamiodanaka, Nakahara-ku, Kawasaki City, Kanagawa Within Fujitsu Limited
Claims (5)
において、バインダ樹脂の損失誘電率に対するトナーの
損失誘電率の比が1.2〜2.3の範囲にあることを特
徴とする電子写真用トナー。1. A dry toner containing a binder resin as a main component, wherein the ratio of the loss permittivity of the toner to the loss permittivity of the binder resin is in the range of 1.2 to 2.3. toner.
であることを特徴とする請求項1記載の電子写真用トナ
ー。2. The electrophotographic toner according to claim 1, wherein the binder resin of the toner is a polyester resin.
とニグロシン系染料を含むことを特徴とする請求項1又
は2記載の電子写真用トナー。3. The toner for electrophotography according to claim 1, wherein carbon and a nigrosine dye are contained as essential constituents of the toner.
と第4級アンモニウム塩系染料を含むことを特徴とする
請求項1,2又は3記載の電子写真用トナー。4. The toner for electrophotography according to claim 1, wherein carbon and a quaternary ammonium salt dye are contained as essential constituents of the toner.
している電子写真に使用する請求項1,2,3又は4記
載の電子写真用トナー。5. The toner for electrophotography according to claim 1, which is used in electrophotography in which a flash fixing system is adopted for toner fixing.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7059434A JPH08254852A (en) | 1995-03-17 | 1995-03-17 | Electrophotographic toner |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7059434A JPH08254852A (en) | 1995-03-17 | 1995-03-17 | Electrophotographic toner |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH08254852A true JPH08254852A (en) | 1996-10-01 |
Family
ID=13113172
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP7059434A Pending JPH08254852A (en) | 1995-03-17 | 1995-03-17 | Electrophotographic toner |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH08254852A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2000004423A1 (en) * | 1998-07-14 | 2000-01-27 | Sanyo Chemical Industries, Ltd. | Tonner binder and tonner |
US6605225B1 (en) * | 1999-01-26 | 2003-08-12 | Japan Science And Technology Corporation | Method and apparatus for fabricating three dimensional element from anisotropic material |
CN1300642C (en) * | 1997-02-12 | 2007-02-14 | 东丽工程株式会社 | Toner composition for developing electrostatic latent image |
-
1995
- 1995-03-17 JP JP7059434A patent/JPH08254852A/en active Pending
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1300642C (en) * | 1997-02-12 | 2007-02-14 | 东丽工程株式会社 | Toner composition for developing electrostatic latent image |
WO2000004423A1 (en) * | 1998-07-14 | 2000-01-27 | Sanyo Chemical Industries, Ltd. | Tonner binder and tonner |
US6605225B1 (en) * | 1999-01-26 | 2003-08-12 | Japan Science And Technology Corporation | Method and apparatus for fabricating three dimensional element from anisotropic material |
WO2004097951A1 (en) * | 1999-01-26 | 2004-11-11 | Tsutomu Yamashita | Method for manufacturing three-dimensional electronic device made or anisotropic material to be processed and its manufacturing apparatus |
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