JP3136792B2 - Toner for developing electrostatic images - Google Patents
Toner for developing electrostatic imagesInfo
- Publication number
- JP3136792B2 JP3136792B2 JP04237031A JP23703192A JP3136792B2 JP 3136792 B2 JP3136792 B2 JP 3136792B2 JP 04237031 A JP04237031 A JP 04237031A JP 23703192 A JP23703192 A JP 23703192A JP 3136792 B2 JP3136792 B2 JP 3136792B2
- Authority
- JP
- Japan
- Prior art keywords
- toner
- parts
- exemplified compound
- present
- group
- 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
Links
- 229920005989 resin Polymers 0.000 claims description 11
- 239000011347 resin Substances 0.000 claims description 11
- 239000003086 colorant Substances 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 description 21
- 239000003795 chemical substances by application Substances 0.000 description 12
- 229920001542 oligosaccharide Polymers 0.000 description 11
- 238000000034 method Methods 0.000 description 10
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 7
- 125000000217 alkyl group Chemical group 0.000 description 5
- 239000000975 dye Substances 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 125000002252 acyl group Chemical group 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- -1 Alternatively Chemical compound 0.000 description 2
- SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 description 2
- 229930091371 Fructose Natural products 0.000 description 2
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 2
- 239000005715 Fructose Substances 0.000 description 2
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 description 2
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000008103 glucose Substances 0.000 description 2
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 150000002772 monosaccharides Chemical class 0.000 description 2
- 108091008695 photoreceptors Proteins 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- HFGHRUCCKVYFKL-UHFFFAOYSA-N 4-ethoxy-2-piperazin-1-yl-7-pyridin-4-yl-5h-pyrimido[5,4-b]indole Chemical compound C1=C2NC=3C(OCC)=NC(N4CCNCC4)=NC=3C2=CC=C1C1=CC=NC=C1 HFGHRUCCKVYFKL-UHFFFAOYSA-N 0.000 description 1
- 229920000858 Cyclodextrin Polymers 0.000 description 1
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- PYMYPHUHKUWMLA-WDCZJNDASA-N arabinose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)C=O PYMYPHUHKUWMLA-WDCZJNDASA-N 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 125000004063 butyryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 229930182830 galactose Natural products 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- AYOOGWWGECJQPI-NSHDSACASA-N n-[(1s)-1-(5-fluoropyrimidin-2-yl)ethyl]-3-(3-propan-2-yloxy-1h-pyrazol-5-yl)imidazo[4,5-b]pyridin-5-amine Chemical compound N1C(OC(C)C)=CC(N2C3=NC(N[C@@H](C)C=4N=CC(F)=CN=4)=CC=C3N=C2)=N1 AYOOGWWGECJQPI-NSHDSACASA-N 0.000 description 1
- VOVZXURTCKPRDQ-CQSZACIVSA-N n-[4-[chloro(difluoro)methoxy]phenyl]-6-[(3r)-3-hydroxypyrrolidin-1-yl]-5-(1h-pyrazol-5-yl)pyridine-3-carboxamide Chemical compound C1[C@H](O)CCN1C1=NC=C(C(=O)NC=2C=CC(OC(F)(F)Cl)=CC=2)C=C1C1=CC=NN1 VOVZXURTCKPRDQ-CQSZACIVSA-N 0.000 description 1
- XULSCZPZVQIMFM-IPZQJPLYSA-N odevixibat Chemical compound C12=CC(SC)=C(OCC(=O)N[C@@H](C(=O)N[C@@H](CC)C(O)=O)C=3C=CC(O)=CC=3)C=C2S(=O)(=O)NC(CCCC)(CCCC)CN1C1=CC=CC=C1 XULSCZPZVQIMFM-IPZQJPLYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000012643 polycondensation polymerization Methods 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 1
- KMIOJWCYOHBUJS-HAKPAVFJSA-N vorolanib Chemical compound C1N(C(=O)N(C)C)CC[C@@H]1NC(=O)C1=C(C)NC(\C=C/2C3=CC(F)=CC=C3NC\2=O)=C1C KMIOJWCYOHBUJS-HAKPAVFJSA-N 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Landscapes
- Developing Agents For Electrophotography (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明は、電子複写機等で使用さ
れる静電荷像現像用トナーに関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an electrostatic image developing toner used in an electronic copying machine or the like.
【0002】[0002]
【従来の技術】電子複写機等で使用される現像剤は、そ
の現像工程において、例えば静電荷像が形成されている
感光体等の像担持体に一旦付着せしめられ、次に転写工
程において感光体から転写紙に転写された後、定着工程
においてコピー紙面に定着される。その際、潜像保持面
上に形成される静電荷像を現像するための現像剤とし
て、キャリアとトナーとから成る二成分系現像剤、およ
びキャリアを必要としない一成分系現像剤(磁性トナ
ー)が知られている。2. Description of the Related Art In a developing process, a developer used in an electronic copying machine or the like is once adhered to an image carrier such as a photoreceptor on which an electrostatic image is formed, and then is exposed to light in a transfer process. After being transferred from the body to the transfer paper, it is fixed on the copy paper surface in a fixing step. At this time, as a developer for developing an electrostatic image formed on the latent image holding surface, a two-component developer including a carrier and a toner and a one-component developer (magnetic toner) that does not require a carrier are used. )It has been known.
【0003】そして、従来より現像剤に帯電性を付与す
るものとしてニグロシン系染料、4級アンモニウム塩、
含金属錯塩染料等の帯電制御剤やキャリアのコーティン
グ剤等が知られていた。しかしながら、これら従来の帯
電性付与剤は、帯電性付与効果が必ずしも十分ではなく
特に該効果が経時変化する為に連続複写によるコピー汚
れが発生し、コピー品質が低下するという問題点を有し
ていた。[0003] Conventionally, a nigrosine dye, a quaternary ammonium salt,
Charge control agents such as metal-containing complex dyes and carrier coating agents have been known. However, these conventional charge-imparting agents have a problem that the effect of imparting charge is not always sufficient, and in particular, the effect changes with time, so that copy smearing due to continuous copying occurs and the copy quality is reduced. Was.
【0004】[0004]
【発明が解決しようとする課題】本発明の目的は、時間
を経てもコピー汚れ等の発生しにくい高品質の静電荷像
現像用トナーを提供することにある。SUMMARY OF THE INVENTION An object of the present invention is to provide a high-quality toner for developing an electrostatic image which is less likely to cause copy stains and the like over time.
【0005】[0005]
【問題点を解決するための手段】本発明者等は上記課題
を解決する為、鋭意検討を行なった結果、特定の構造を
有する化合物をトナー中に含有させることにより、これ
らの問題点が解決されることを見い出し、本発明に到達
した。すなわち、本発明は、少なくとも樹脂及び着色剤
を含有してなる静電荷像現像用トナーにおいて、サイク
ロオリゴ糖又はその誘導体を一種以上含有することを特
徴とする静電荷像現像用トナーである。Means for Solving the Problems The present inventors have conducted intensive studies in order to solve the above-mentioned problems, and as a result, by incorporating a compound having a specific structure into the toner, these problems have been solved. And arrived at the present invention. That is, the present invention relates to an electrostatic image developing toner containing at least a resin and a colorant, wherein the toner comprises at least one cyclo-oligosaccharide or a derivative thereof.
【0006】以下、本発明を詳細に説明する。本発明の
静電荷像現像用トナーは、サイクロオリゴ糖又はその誘
導体を1種以上含有することを特徴とする。サイクロオ
リゴ糖とは、一般に単糖類が水分子を失なって6個ない
し8個環状に縮重合したものをさす。サイクロオリゴ糖
を構成する単糖類としては、グルコース、フルクトー
ス、キシロース、ガラクトース、マンノース、アラビノ
ースなどが挙げられる。Hereinafter, the present invention will be described in detail. The electrostatic image developing toner of the present invention is characterized by containing one or more cyclooligosaccharides or derivatives thereof. The cyclo-oligosaccharide generally refers to a monosaccharide obtained by condensation polymerization of 6 to 8 cyclic molecules due to loss of water molecules. Examples of the monosaccharide constituting the cyclo-oligosaccharide include glucose, fructose, xylose, galactose, mannose and arabinose.
【0007】本発明に用いられるサイクロオリゴ糖とし
ては、フルクトースから成るサイクロイヌロオリゴ糖、
若しくはグルコースから成るサイクロデキストリン又は
その誘導体が特に好適であり、下記一般式(I)又は
(II) で表わされる化合物である。The cyclo-oligosaccharides used in the present invention include cycloinulo-oligosaccharides composed of fructose,
Alternatively, cyclodextrin composed of glucose or a derivative thereof is particularly preferable, and is a compound represented by the following general formula (I) or (II).
【0008】[0008]
【化1】 Embedded image
【0009】〔式中、R1 ,R2 及びR3 は、それぞ
れ、水素原子、アルキル基、アシル基、等を表わし、n
は6〜8のいずれかの数を表わす。またR1 ,R2 ,R
3 はすべて同一であっても異っていてもよい。〕Wherein R 1 , R 2 and R 3 each represent a hydrogen atom, an alkyl group, an acyl group or the like;
Represents a number from 6 to 8. R 1 , R 2 , R
All three may be the same or different. ]
【0010】[0010]
【化2】 Embedded image
【0011】〔式中、R4 ,R5 及びR6 は、それぞ
れ、水素原子、アルキル基、又はアシル基等を表わし、
mは6〜8のいずれかの数を表わす。またR4 ,R5 ,
R6 はすべて同一であっても異っていてもよい。〕置換
基R1 ,R2 ,R3 の具体例をあげれば、水素原子;メ
チル基,エチル基,プロピル基,ブチル基等のアルキル
基;アセチル基,プロピオニル基,ブチリル基,イソブ
チリル基等のアシル基が挙げられ、中でもR1 が水素原
子,R2 ,R3 がメチル基が好ましい。またnについて
は6が好ましい。Wherein R 4 , R 5 and R 6 each represent a hydrogen atom, an alkyl group, an acyl group or the like;
m represents any number from 6 to 8. R 4 , R 5 ,
R 6 may be all the same or different. Specific examples of the substituents R 1 , R 2 and R 3 include a hydrogen atom; an alkyl group such as a methyl group, an ethyl group, a propyl group and a butyl group; An acyl group is mentioned, and among them, R 1 is preferably a hydrogen atom, and R 2 and R 3 are preferably methyl groups. Also, n is preferably 6.
【0012】置換基R4 ,R5 ,R6 の具体例をあげれ
ば、水素原子;メチル基,エチル基,プロピル基,ブチ
ル基等のアルキル基;アセチル基,プロピオニル基,ブ
チリル基,イソブチリル基等のアシル基が挙げられ、中
でもR4 が水素原子,R5 ,R6 がメチル基が好まし
い。またmについては6が好ましい。また、R1 ,
R2 ,R3 が全て水素原子の場合には、水溶性が高くな
り電気特性に若干問題が生じる可能性がある。Specific examples of the substituents R 4 , R 5 and R 6 include a hydrogen atom; an alkyl group such as a methyl group, an ethyl group, a propyl group and a butyl group; an acetyl group, a propionyl group, a butyryl group and an isobutyryl group. R 4 is preferably a hydrogen atom, and R 5 and R 6 are preferably methyl groups. Also, m is preferably 6. Also, R 1 ,
When R 2 and R 3 are all hydrogen atoms, the solubility in water becomes high, and there is a possibility that a slight problem may occur in the electric characteristics.
【0013】一般式(I)あるいは(II)で表わされる
サイクロオリゴ糖又はその誘導体の中で本発明の静電荷
像用トナーに含有せしめるのに好適なものの具体例とし
ては下記の構造式で表わされる化合物を挙げることがで
きるが、これらに限定されるものではない。Among the cyclo-oligosaccharides or derivatives thereof represented by the general formula (I) or (II), specific examples suitable for inclusion in the toner for electrostatic image of the present invention are represented by the following structural formulas. However, the present invention is not limited thereto.
【0014】[0014]
【表1】 [Table 1]
【0015】このようなサイクロオリゴ糖又はその誘導
体は、その製造法によらず本発明に用いることができる
が、具体的製造方法の一例としては特開平2−2527
01号公報記載の方法が挙げられる。本発明に、使用し
得る樹脂成分としては、静電荷像現像用トナーに適した
公知の種々のものが使用できる。例えば、スチレン系樹
脂、スチレンアクリル系共重合樹脂、ポリエステル系樹
脂、エポキシ系樹脂及びこれらの混合樹脂、また、これ
らのアルキル側鎖にアミノ基を有するもの等がある。[0015] Such cyclo-oligosaccharides or derivatives thereof can be used in the present invention irrespective of the production method, but a specific production method is described in JP-A-2-2527.
No. 01 publication. As the resin component usable in the present invention, various known resin components suitable for the toner for developing an electrostatic image can be used. For example, styrene-based resins, styrene-acrylic copolymer resins, polyester-based resins, epoxy-based resins, and mixed resins thereof, and those having an amino group in the alkyl side chain, and the like are available.
【0016】トナー中のサイクロオリゴ糖又はその誘導
体の含有率は、樹脂100重量部に対して0.1〜20
重量部が好ましく、より好ましくは1〜15重量部であ
る。サイクロオリゴ糖又はその誘導体の含有率が少なす
ぎると帯電性の向上効果が期待できず、また過剰である
とトナーの品質が低下するので好ましくない。本発明で
用いる着色剤としては、従来から用いられているもので
あれば特に制限されるものではなく、黒色トナーを得る
には、カーボンブラック等を使用する。また、サイクロ
オリゴ糖又はその誘導体は、通常白色なので、青、赤、
黄等のカラートナーに含有せしめてもよく、この場合は
相当する色の染顔料等からなる着色剤を用いる。The content of the cyclo-oligosaccharide or a derivative thereof in the toner is 0.1 to 20 parts by weight based on 100 parts by weight of the resin.
It is preferably 1 part by weight, more preferably 1 to 15 parts by weight. If the content of the cyclo-oligosaccharide or a derivative thereof is too small, the effect of improving the chargeability cannot be expected, and if it is excessive, the quality of the toner deteriorates, which is not preferable. The colorant used in the present invention is not particularly limited as long as it is conventionally used, and carbon black or the like is used to obtain a black toner. Cyclo-oligosaccharides or derivatives thereof are usually white, so blue, red,
It may be contained in a color toner such as yellow, and in this case, a colorant comprising a dye or pigment of a corresponding color is used.
【0017】着色剤の含有率は、樹脂100重量部に対
して3〜20重量部とするのが好ましい。更に、本発明
のトナーには、サイクロオリゴ糖又はその誘導体とは別
に、公知のものを含めて他の帯電制御剤、例えば、ニグ
ロシン系染料、4級アンモニウム塩、含金錯素塩染料等
を含有せしめてもよい。The content of the colorant is preferably 3 to 20 parts by weight based on 100 parts by weight of the resin. Further, in addition to the cyclo-oligosaccharide or a derivative thereof, the toner of the present invention may contain other charge control agents including known ones, such as a nigrosine dye, a quaternary ammonium salt, and a gold-containing complex salt dye. May be included.
【0018】その他、本発明のトナー構成成分として、
定着性や流動性を向上させるため、低分子量オレフィン
重合体や微粉末シリカ等の添加剤を含有せしめてもよ
い。トナーの製造法としては、上記の各成分をニーダー
等で混練し冷却後、粉砕し分級すればよい。又、本発明
のトナーは二成分系現像剤の他に、カプセル化トナーや
重合トナー及びマグネタイト含有トナー等のいわゆる一
成分系現像剤(磁性トナー)にも適用することができ
る。Other components of the toner of the present invention include:
In order to improve fixability and fluidity, additives such as a low molecular weight olefin polymer and finely divided silica may be added. The toner may be produced by kneading the above components in a kneader or the like, cooling, pulverizing and classifying. In addition to the two-component developer, the toner of the present invention can be applied to a so-called one-component developer (magnetic toner) such as an encapsulated toner, a polymerized toner, and a magnetite-containing toner.
【0019】トナーの平均粒径は5〜20μmが好適で
ある。本発明のトナーと混合して現像剤を形成するキャ
リアとしては、特に制限はないが10〜200μmの平
均粒径を有する鉄粉が好ましい。なお、鉄粉の粒径には
特に制限はない。この場合、連続使用時の耐久性向上の
目的でフッ素系樹脂等をコーティングしたいわゆるコー
ティングキャリアも使用することができる。又、フェラ
イト系、マグネタイト系等を初めとする公知の他のキャ
リアも使用することができる。これらキャリアは、トナ
ー1重量部に対して、5〜100重量部使用することが
好ましい。The average particle size of the toner is preferably 5 to 20 μm. The carrier for forming the developer by mixing with the toner of the present invention is not particularly limited, but is preferably an iron powder having an average particle diameter of 10 to 200 μm. The particle size of the iron powder is not particularly limited. In this case, a so-called coated carrier coated with a fluorine-based resin or the like for the purpose of improving durability during continuous use can also be used. Further, other known carriers such as a ferrite-based or magnetite-based carrier can also be used. These carriers are preferably used in an amount of 5 to 100 parts by weight based on 1 part by weight of the toner.
【0020】[0020]
【実施例】以下、実施例により本発明を更に詳細に説明
するが、本発明はその要旨を超えない限り、以下の実施
例によりなんら制限されるものではない。なお、下記実
施例中単に「部」とあるのはいずれも「重量部」を意味
するものとする。EXAMPLES The present invention will be described in more detail with reference to the following Examples, which should not be construed as limiting the scope of the invention. In the following examples, “parts” simply means “parts by weight”.
【0021】[0021]
【表2】実施例−1 スチレン系樹脂 100部 (三洋化成社製、商品名SBM−600) カーボンブラック 10部 (三菱化成(株)製#44) 例示化合物(1) 2部Example 1 100 parts of styrene resin (SBM-600, manufactured by Sanyo Kasei Co., Ltd.) 10 parts of carbon black (# 44 manufactured by Mitsubishi Kasei Co., Ltd.) 2 parts of exemplified compound (1)
【0022】上記の材料を配合混練し、粉砕分級して平
均粒子径11μmの黒色正帯電トナーを得た。このトナ
ー5部と平均粒径約100μmのフッ素系樹脂コーティ
ングキャリア100部とを混合攪拌して現像剤を作製し
た。次いでこの現像剤を有機光導電体を感光体とする複
写機で実写したところ白地部の地汚れ、いわゆるカブリ
の少ない鮮明なコピーが得られた。The above-mentioned materials were mixed and kneaded, and pulverized and classified to obtain a black positively charged toner having an average particle diameter of 11 μm. 5 parts of this toner and 100 parts of a fluororesin-coated carrier having an average particle diameter of about 100 μm were mixed and stirred to prepare a developer. Next, when this developer was actually photographed with a copying machine using an organic photoconductor as a photoreceptor, a clear copy with less background stains, so-called fog, was obtained.
【0023】実施例−2 帯電制御剤として、例示化合物(1)2部のかわりに例
示化合物(2)を1部使用する以外は、実施例−1と全
く同様にしたところ、実施例−1と同様に良好なコピー
が得られた。Example 2 The procedure of Example 1 was repeated, except that 1 part of Exemplified Compound (2) was used instead of 2 parts of Exemplified Compound (1) as a charge controlling agent. A good copy was obtained in the same manner as described above.
【0024】実施例−3 帯電制御剤として、例示化合物(1)2部のかわりに例
示化合物(4)を3部使用する以外は、実施例−1と全
く同様にしたところ、実施例−1と同様に良好なコピー
が得られた。Example 3 The procedure of Example 1 was repeated, except that 3 parts of Exemplified Compound (4) was used instead of 2 parts of Exemplified Compound (1) as a charge controlling agent. A good copy was obtained in the same manner as described above.
【0025】実施例−4 帯電制御剤として、例示化合物(1)2部のかわりに例
示化合物(7)を5部使用する以外は、実施例−1と全
く同様にしたところ、実施例−1と同様に良好なコピー
が得られた。Example 4 The procedure of Example 1 was repeated except that 5 parts of Exemplified Compound (7) was used instead of 2 parts of Exemplified Compound (1) as a charge controlling agent. A good copy was obtained in the same manner as described above.
【0026】実施例−5 帯電制御剤として、例示化合物(1)2部のかわりに例
示化合物(10)を3部使用する以外は、実施例−1と
全く同様にしたところ、実施例−1と同様に良好なコピ
ーが得られた。Example-5 Except that 3 parts of Exemplified Compound (10) was used instead of 2 parts of Exemplified Compound (1) as a charge controlling agent, the procedure of Example-1 was repeated. A good copy was obtained in the same manner as described above.
【0027】実施例−6 帯電制御剤として、例示化合物(1)2部のかわりに例
示化合物(11)を2部使用する以外は、実施例−1と
全く同様にしたところ、実施例−1と同様に良好なコピ
ーが得られた。Example -6 The same procedure as in Example 1 was carried out except that 2 parts of Exemplified Compound (11) was used instead of 2 parts of Exemplified Compound (1) as a charge controlling agent. A good copy was obtained in the same manner as described above.
【0028】実施例−7 帯電制御剤として、例示化合物(1)2部のかわりに例
示化合物(13)を3部使用する以外は、実施例−1と
全く同様にしたところ、実施例−1と同様に良好なコピ
ーが得られた。Example -7 The same procedures as in Example 1 were carried out except that 3 parts of Exemplified Compound (13) were used instead of 2 parts of Exemplified Compound (1) as a charge controlling agent. A good copy was obtained in the same manner as described above.
【0029】実施例−8 帯電制御剤として、例示化合物(1)2部のかわりに例
示化合物(16)を4部使用する以外は、実施例−1と
全く同様にしたところ、実施例−1と同様に良好なコピ
ーが得られた。Example-8 Except that 4 parts of Exemplified Compound (16) was used instead of 2 parts of Exemplified Compound (1) as a charge controlling agent, the procedure of Example 1 was repeated. A good copy was obtained in the same manner as described above.
【0030】実施例−9 帯電制御剤として、例示化合物(1)2部のかわりに例
示化合物(18)を3部使用する以外は、実施例−1と
全く同様にしたところ、実施例−1と同様に良好なコピ
ーが得られた。Example -9 Example 1 was carried out in exactly the same manner as in Example 1 except that 3 parts of Exemplified Compound (18) was used instead of 2 parts of Exemplified Compound (1) as a charge controlling agent. A good copy was obtained in the same manner as described above.
【0031】実施例−10 帯電制御剤として、例示化合物(1)2部のかわりに例
示化合物(20)を4部使用する以外は、実施例−1と
全く同様にしたところ、実施例−1と同様に良好なコピ
ーが得られた。Example 10 The procedure of Example 1 was repeated, except that 4 parts of Exemplified Compound (20) were used instead of 2 parts of Exemplified Compound (1) as a charge controlling agent. A good copy was obtained in the same manner as described above.
【0032】[0032]
【発明の効果】本発明の静電荷像現像用トナーは、連続
複写によるコピーの汚れ等の発生しない高品質の静電荷
像現像用トナーである。The toner for developing an electrostatic image of the present invention is a high-quality toner for developing an electrostatic image, which does not cause stains on a copy in continuous copying.
フロントページの続き (58)調査した分野(Int.Cl.7,DB名) G03G 9/08 Continuation of front page (58) Field surveyed (Int.Cl. 7 , DB name) G03G 9/08
Claims (1)
る静電荷像現像用トナーにおいて、サイクロオリゴ糖又
はその誘導体を1種以上含有することを特徴とする静電
荷像現像用トナー。1. An electrostatic image developing toner comprising at least a resin and a colorant, comprising at least one cyclooligosaccharide or a derivative thereof.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP04237031A JP3136792B2 (en) | 1992-09-04 | 1992-09-04 | Toner for developing electrostatic images |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP04237031A JP3136792B2 (en) | 1992-09-04 | 1992-09-04 | Toner for developing electrostatic images |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH06124002A JPH06124002A (en) | 1994-05-06 |
| JP3136792B2 true JP3136792B2 (en) | 2001-02-19 |
Family
ID=17009373
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP04237031A Expired - Fee Related JP3136792B2 (en) | 1992-09-04 | 1992-09-04 | Toner for developing electrostatic images |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3136792B2 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4418842A1 (en) * | 1994-05-30 | 1995-12-07 | Hoechst Ag | Colourless, thermostable, non-toxic cyclised oligo- or poly:saccharide use as charge controller or enhancer |
| US5627002A (en) * | 1996-08-02 | 1997-05-06 | Xerox Corporation | Liquid developer compositions with cyclodextrins |
| CN102741258B (en) | 2009-06-17 | 2015-09-30 | 德州大学体系董事会 | Composition and method of cyclofructan as separating agent |
-
1992
- 1992-09-04 JP JP04237031A patent/JP3136792B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH06124002A (en) | 1994-05-06 |
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| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |