JPH03125156A - Toner for electrophotograhy - Google Patents
Toner for electrophotograhyInfo
- Publication number
- JPH03125156A JPH03125156A JP1262867A JP26286789A JPH03125156A JP H03125156 A JPH03125156 A JP H03125156A JP 1262867 A JP1262867 A JP 1262867A JP 26286789 A JP26286789 A JP 26286789A JP H03125156 A JPH03125156 A JP H03125156A
- Authority
- JP
- Japan
- Prior art keywords
- toner
- wax
- coating
- core
- consequently
- 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
- 239000003086 colorant Substances 0.000 claims abstract description 7
- 229920005992 thermoplastic resin Polymers 0.000 claims abstract description 5
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- 230000006866 deterioration Effects 0.000 abstract description 6
- 239000007788 liquid Substances 0.000 abstract description 2
- 238000007786 electrostatic charging Methods 0.000 abstract 1
- 238000000926 separation method Methods 0.000 abstract 1
- 239000001993 wax Substances 0.000 description 15
- 229920005989 resin Polymers 0.000 description 14
- 239000011347 resin Substances 0.000 description 14
- 238000000034 method Methods 0.000 description 11
- 239000002245 particle Substances 0.000 description 11
- 238000005299 abrasion Methods 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 7
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- 108091008695 photoreceptors Proteins 0.000 description 6
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 5
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- 230000000052 comparative effect Effects 0.000 description 4
- 238000011161 development Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 239000006229 carbon black Substances 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 239000007822 coupling agent Substances 0.000 description 3
- 238000004898 kneading Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- UAJRSHJHFRVGMG-UHFFFAOYSA-N 1-ethenyl-4-methoxybenzene Chemical compound COC1=CC=C(C=C)C=C1 UAJRSHJHFRVGMG-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
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- 239000000155 melt Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- JKQOBWVOAYFWKG-UHFFFAOYSA-N molybdenum trioxide Chemical compound O=[Mo](=O)=O JKQOBWVOAYFWKG-UHFFFAOYSA-N 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
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- 239000000126 substance Substances 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- BJQFWAQRPATHTR-UHFFFAOYSA-N 1,2-dichloro-4-ethenylbenzene Chemical compound ClC1=CC=C(C=C)C=C1Cl BJQFWAQRPATHTR-UHFFFAOYSA-N 0.000 description 1
- QOVCUELHTLHMEN-UHFFFAOYSA-N 1-butyl-4-ethenylbenzene Chemical compound CCCCC1=CC=C(C=C)C=C1 QOVCUELHTLHMEN-UHFFFAOYSA-N 0.000 description 1
- KTZVZZJJVJQZHV-UHFFFAOYSA-N 1-chloro-4-ethenylbenzene Chemical compound ClC1=CC=C(C=C)C=C1 KTZVZZJJVJQZHV-UHFFFAOYSA-N 0.000 description 1
- DMADTXMQLFQQII-UHFFFAOYSA-N 1-decyl-4-ethenylbenzene Chemical compound CCCCCCCCCCC1=CC=C(C=C)C=C1 DMADTXMQLFQQII-UHFFFAOYSA-N 0.000 description 1
- WJNKJKGZKFOLOJ-UHFFFAOYSA-N 1-dodecyl-4-ethenylbenzene Chemical compound CCCCCCCCCCCCC1=CC=C(C=C)C=C1 WJNKJKGZKFOLOJ-UHFFFAOYSA-N 0.000 description 1
- OEVVKKAVYQFQNV-UHFFFAOYSA-N 1-ethenyl-2,4-dimethylbenzene Chemical compound CC1=CC=C(C=C)C(C)=C1 OEVVKKAVYQFQNV-UHFFFAOYSA-N 0.000 description 1
- JZHGRUMIRATHIU-UHFFFAOYSA-N 1-ethenyl-3-methylbenzene Chemical compound CC1=CC=CC(C=C)=C1 JZHGRUMIRATHIU-UHFFFAOYSA-N 0.000 description 1
- WHFHDVDXYKOSKI-UHFFFAOYSA-N 1-ethenyl-4-ethylbenzene Chemical compound CCC1=CC=C(C=C)C=C1 WHFHDVDXYKOSKI-UHFFFAOYSA-N 0.000 description 1
- LCNAQVGAHQVWIN-UHFFFAOYSA-N 1-ethenyl-4-hexylbenzene Chemical compound CCCCCCC1=CC=C(C=C)C=C1 LCNAQVGAHQVWIN-UHFFFAOYSA-N 0.000 description 1
- LUWBJDCKJAZYKZ-UHFFFAOYSA-N 1-ethenyl-4-nonylbenzene Chemical compound CCCCCCCCCC1=CC=C(C=C)C=C1 LUWBJDCKJAZYKZ-UHFFFAOYSA-N 0.000 description 1
- HLRQDIVVLOCZPH-UHFFFAOYSA-N 1-ethenyl-4-octylbenzene Chemical compound CCCCCCCCC1=CC=C(C=C)C=C1 HLRQDIVVLOCZPH-UHFFFAOYSA-N 0.000 description 1
- QEDJMOONZLUIMC-UHFFFAOYSA-N 1-tert-butyl-4-ethenylbenzene Chemical compound CC(C)(C)C1=CC=C(C=C)C=C1 QEDJMOONZLUIMC-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- RBTBFTRPCNLSDE-UHFFFAOYSA-N 3,7-bis(dimethylamino)phenothiazin-5-ium Chemical compound C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 RBTBFTRPCNLSDE-UHFFFAOYSA-N 0.000 description 1
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
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- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- 229910000420 cerium oxide Inorganic materials 0.000 description 1
- 239000012986 chain transfer agent Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 108010023700 galanin-(1-13)-bradykinin-(2-9)-amide Proteins 0.000 description 1
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- PBZROIMXDZTJDF-UHFFFAOYSA-N hepta-1,6-dien-4-one Chemical compound C=CCC(=O)CC=C PBZROIMXDZTJDF-UHFFFAOYSA-N 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
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- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
- 229910052809 inorganic oxide Inorganic materials 0.000 description 1
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 1
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- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
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- 239000000178 monomer Substances 0.000 description 1
- NZIDBRBFGPQCRY-UHFFFAOYSA-N octyl 2-methylprop-2-enoate Chemical compound CCCCCCCCOC(=O)C(C)=C NZIDBRBFGPQCRY-UHFFFAOYSA-N 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 1
- HDBWAWNLGGMZRQ-UHFFFAOYSA-N p-Vinylbiphenyl Chemical compound C1=CC(C=C)=CC=C1C1=CC=CC=C1 HDBWAWNLGGMZRQ-UHFFFAOYSA-N 0.000 description 1
- UCUUFSAXZMGPGH-UHFFFAOYSA-N penta-1,4-dien-3-one Chemical class C=CC(=O)C=C UCUUFSAXZMGPGH-UHFFFAOYSA-N 0.000 description 1
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- 229940051201 quinoline yellow Drugs 0.000 description 1
- 235000012752 quinoline yellow Nutrition 0.000 description 1
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- 229920002545 silicone oil Polymers 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 229920006249 styrenic copolymer Polymers 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- FUSUHKVFWTUUBE-UHFFFAOYSA-N vinyl methyl ketone Natural products CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- XOSXWYQMOYSSKB-LDKJGXKFSA-L water blue Chemical compound CC1=CC(/C(\C(C=C2)=CC=C2NC(C=C2)=CC=C2S([O-])(=O)=O)=C(\C=C2)/C=C/C\2=N\C(C=C2)=CC=C2S([O-])(=O)=O)=CC(S(O)(=O)=O)=C1N.[Na+].[Na+] XOSXWYQMOYSSKB-LDKJGXKFSA-L 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Landscapes
- Developing Agents For Electrophotography (AREA)
Abstract
Description
【発明の詳細な説明】
[発明の目的]
(産業上の利用分野)
本発明は、加熱ローラ定着方法に好適な電子写真用トナ
ーに関する。DETAILED DESCRIPTION OF THE INVENTION [Object of the Invention] (Field of Industrial Application) The present invention relates to an electrophotographic toner suitable for a heating roller fixing method.
(従来の技術)
一般に、電子写真複写機を用いることにより、感光体ド
ラム上に形成された静電潜像をトナーにより可視像化し
、この可視像を転写紙に転写した後、定着して複写画像
を得ることができる。この静電潜像を現像する方法とし
ては、磁気ブラシ現像方法、カスケード現像方法、ファ
ーブラシ現像方法、パウダークラウド法等が知られてい
るが、これらの方法では、使用されるトナーが、現像機
内で激しい機械的衝撃力を繰り返し受けるために、数千
回の現像後には劣化して微細なトナーが発生する。これ
により画像上にカブリが出現したり、この微細なトナー
がキャリヤ表面へ融着することにより摩擦帯電性が低下
する等の悪影響を及ぼす。(Prior Art) Generally, by using an electrophotographic copying machine, an electrostatic latent image formed on a photoreceptor drum is made visible using toner, and after this visible image is transferred to transfer paper, it is fixed. A copy image can be obtained by As methods for developing this electrostatic latent image, there are known methods such as a magnetic brush development method, a cascade development method, a fur brush development method, and a powder cloud method, but in these methods, the toner used is Because it is repeatedly subjected to severe mechanical impact, it deteriorates and produces fine toner particles after several thousand times of development. This causes negative effects such as fogging on the image and a reduction in triboelectric charging properties due to the fine toner being fused onto the surface of the carrier.
このようなトナーの劣化には、機械的な摩耗に対して強
靭な樹脂、即ち分子量の大きな樹脂、架橋された樹脂等
をトナーの結′着樹脂として用いることが有効である。To prevent such toner deterioration, it is effective to use a resin that is strong against mechanical abrasion, that is, a resin with a large molecular weight, a crosslinked resin, etc., as a binder resin for the toner.
しかし、これらの樹脂は、一般に高融点であり、弾性が
大きく、転写紙との親和性に乏しい。そのため、これら
の樹脂をトナーの結着樹脂として用いた場合、トナーを
被転写体と十分に定着させるためには、多くの熱エネル
ギーを効率良く与える必要がある。However, these resins generally have a high melting point, high elasticity, and poor affinity with transfer paper. Therefore, when these resins are used as binder resins for toner, it is necessary to efficiently apply a large amount of thermal energy in order to sufficiently fix the toner to the transfer target.
熱効率の良い定着方法としては、加熱ローラによる接触
型の加熱定着が良く知られ、現在、非常に多く用いられ
ている。しかしながら、この加熱ローラを用いると、加
熱、ローラが直接トナーと接触するために、加熱ロー′
う“表面″・に溶融したトーナーが付着し、この加2′
熱ローラから後続の被転写体に付着して汚れが発生する
現象いわゆるオフセット現象を生じやすい。この、現象
を防ぐたあ“に″、ローラ表面°をフッ素系樹1・、゛
シリ、コンオ゛イルな゛ど:の・離型性に優れた材質で
被゛薯するな、ど、定着ローラ表面にトナーが付着し゛
な′いよ・うにすることが考えられる。しかし、な・が
ら1.、これ、らの材質は、高温環境下の連続使用に゛
おける耐久性及び保存性に問題がある。Contact-type heat fixing using a heating roller is well known as a fixing method with good thermal efficiency, and is currently widely used. However, when this heating roller is used, the heating roller comes into direct contact with the toner, so the heating roller
The molten toner adheres to the “surface” and this
A so-called offset phenomenon is likely to occur, which is a phenomenon in which dirt adheres from the heat roller to the subsequent transfer target. In order to prevent this phenomenon, the roller surface should be coated with a material with excellent mold release properties such as fluorine-based resin, silicone, oil, etc. One idea is to prevent toner from adhering to the roller surface. However, 1. These materials have problems in durability and storage stability when used continuously in high-temperature environments.
また、上記°のような融点−の高い樹脂を含有したトナ
ーを十分に定着させるためには、加熱ローラの温度を高
くする必要があるこ°・とから、転写坂・の焦げ、カー
ルが発生したり、定着器の材質が制限されたり、また大
きな電力を必要とする等の間履を生ずる。このため、電
子写真用゛トナーは、機械的な摩耗に強靭であり、かつ
比較的低温で被写体に融着するものであることが望まし
い。比較的低温で融着可能であるためには、分子量の小
さい樹脂を用いればよいが、このようなトナーは耐摩耗
性が劣り、劣化防止という目的に相反してしまう。In addition, in order to sufficiently fix toner containing a resin with a high melting point such as the one mentioned above, it is necessary to raise the temperature of the heating roller, which may cause scorching and curling of the transfer slope. In addition, the material of the fixing device is limited, and a large amount of electric power is required. For this reason, it is desirable that toner for electrophotography be resistant to mechanical abrasion and fused to the subject at a relatively low temperature. In order to be able to fuse at a relatively low temperature, a resin with a small molecular weight may be used, but such a toner has poor abrasion resistance, which contradicts the purpose of preventing deterioration.
さらに、一般に電子写真用トナーでは定着性を向上させ
るためには溶融粘度が低いものが要求される。その理由
は、トナーの溶融粘度が高すぎると、トナーの支持体に
対する親和性が乏しくなり、トナーが支持体に融着せず
低温オフセット等を発生、す゛るためである。一方、ト
ナーの溶融粘度が低いと・、トナーの支持体に対する親
和性は良好となるが一トナー全部τが支持体に融着せず
に加熱ローラ上、に残るため、逆に高温オフセット等を
発生する場合がある。このように、オフセット現象を起
こさずに、優れた定着性を有する電子写真用トナーを製
造するのは困難であった。Further, toner for electrophotography is generally required to have a low melt viscosity in order to improve fixing properties. The reason for this is that if the melt viscosity of the toner is too high, the affinity of the toner with the support will be poor, and the toner will not be fused to the support, resulting in low-temperature offset and the like. On the other hand, if the melt viscosity of the toner is low, the affinity of the toner to the support is good, but all of the toner τ remains on the heating roller without being fused to the support, resulting in high-temperature offset, etc. There are cases where As described above, it has been difficult to produce an electrophotographic toner with excellent fixing properties without causing the offset phenomenon.
そこで、近年トナー中にワックスを添加し、耐オフセッ
ト性及び被写体との親和性を向上することが提案されて
いる。しかしながら、このようなトナーに十分な定着性
を付与するためには、過剰な量のワックスが必要となり
、高温時のトナーのケーキ化、流動性及びこれによる帯
電性の低下、感光体上のフィルミングの形成等の弊害が
生じる。Therefore, in recent years, it has been proposed to add wax to toner to improve offset resistance and compatibility with the subject. However, in order to impart sufficient fixing properties to such toners, an excessive amount of wax is required, resulting in toner caking at high temperatures, a decrease in fluidity and resulting chargeability, and problems with the film on the photoreceptor. This causes harmful effects such as the formation of scratches.
(発明が解決しようとする課題)
そこで本発明は、上記課題を解決するために、ワックス
を添加することにより生じる高温時のトナーのケーキ化
、流動性の悪化及びこれに伴う帯電性の低下、及び感光
体上のフィルミング形成等の弊害を最小限に押さえ、耐
オフセット性に優れ、機械的な摩耗に強靭であり、かつ
定着性が良好な電子写真用トナーを提供することを目的
とする。(Problems to be Solved by the Invention) Therefore, in order to solve the above-mentioned problems, the present invention solves the problem of toner cake formation at high temperatures caused by adding wax, deterioration of fluidity, and accompanying decrease in chargeability. The purpose of the present invention is to provide an electrophotographic toner that minimizes adverse effects such as the formation of filming on a photoreceptor, has excellent offset resistance, is strong against mechanical abrasion, and has good fixing properties. .
また二本発明の他の目的は、カブリが少なく鮮明な転写
画像が得られる電子写真用トナーを提供することである
。Another object of the present invention is to provide an electrophotographic toner that can produce clear transferred images with less fog.
[発明の構成]
(課題を解決するための手段)
本発明のトナーは、トナー成分として熱可塑性樹脂及び
着色剤を含む核トナーと、この核トナー表面を被覆する
該トナー成分及びワックスを含む被覆トナーとを含有し
、かつ前記ワックスが被覆トナー中に1ないし80重量
%含まれることを特徴とする。[Structure of the Invention] (Means for Solving the Problems) The toner of the present invention comprises a core toner containing a thermoplastic resin and a colorant as toner components, and a coating containing the toner components and wax that covers the surface of the core toner. toner, and the wax is contained in the coated toner in an amount of 1 to 80% by weight.
本発明に用いられるワックスとしては、低分子量ポリプ
ロピレン、低分子量ポリエチレン及び低分子オレフィン
共重合体等をあげることができる。Examples of the wax used in the present invention include low molecular weight polypropylene, low molecular weight polyethylene, and low molecular weight olefin copolymers.
このようなワックスは、被覆トナー中に1〜80重量%
含まれており、1重量%未満であると、定着性、耐オフ
セット性が不十分であり、80ffl量%を超えると、
高温時のケーキ化、流動性の低下、感光体のフィルミン
グ形成等の弊害をまねく傾向がある。Such waxes may be present in the coated toner in an amount of 1 to 80% by weight.
If it is less than 1% by weight, the fixing properties and anti-offset properties will be insufficient, and if it exceeds 80ffl%,
This tends to cause problems such as caking at high temperatures, decreased fluidity, and formation of filming on the photoreceptor.
熱可塑性樹脂としてはスチレン、m−メチルスチレン、
0−メチルスチレンp−メチルスチレン、p−エチルス
チレン、2.4−ジメチルスチレン、p−n−ブチルス
チレン、p−n−へキシルスチレン、p−tert−ブ
チルスチレン、p−n−オクチルスチレン、p−n−ノ
ニルスチレン、p−n−デシルスチレン、p−n−ドデ
シルスチレン、p−メトキシスチレン、p−フェニルス
チレン、p−クロルスチレン、3.4−ジクロルスチレ
ン等のスチレン類、アクリル酸、アクリル酸メチル、ア
クリル酸エチル、アクリル酸ブチル、アクリル酸フェニ
ル、メタクリル酸、メタクリル酸メチル、メタクリル酸
エチル、メタクリル酸ブチル、メタクリル酸オクチル、
アクリロニトリル、メタクリルニトリル等の二重結合を
有するモノカルボン酸及びそれらの置換体、ビニルメチ
ルケトン、ビニルエキシルケトン等のビニルケトン類、
ビニルメチルエーテル、ビニルエーテル類、−チル等の
ビニルエーテル類、塩化ビニル、酢酸ビニル、安息香酸
ビニル等のビニルエステル類などの単量体のホモポリマ
ーまたはコポリマー等を使用することができる。また、
樹脂を重合する際に架橋剤や連鎖移動剤を添加して分子
中に分岐を作ることは、樹脂の耐摩耗性が向上すること
から、本発明において特に好ましい。Thermoplastic resins include styrene, m-methylstyrene,
0-methylstyrene p-methylstyrene, p-ethylstyrene, 2,4-dimethylstyrene, p-n-butylstyrene, p-n-hexylstyrene, p-tert-butylstyrene, p-n-octylstyrene, Styrenes such as p-n-nonylstyrene, p-n-decylstyrene, p-n-dodecylstyrene, p-methoxystyrene, p-phenylstyrene, p-chlorostyrene, 3,4-dichlorostyrene, acrylic acid , methyl acrylate, ethyl acrylate, butyl acrylate, phenyl acrylate, methacrylic acid, methyl methacrylate, ethyl methacrylate, butyl methacrylate, octyl methacrylate,
Monocarboxylic acids with double bonds such as acrylonitrile and methacrylonitrile and substituted products thereof, vinyl ketones such as vinyl methyl ketone and vinyl exyl ketone,
Homopolymers or copolymers of monomers such as vinyl ethers such as vinyl methyl ether, vinyl ethers, and -thyl, and vinyl esters such as vinyl chloride, vinyl acetate, and vinyl benzoate can be used. Also,
In the present invention, it is particularly preferable to add a crosslinking agent or a chain transfer agent to create branches in the molecule when polymerizing the resin, since this improves the abrasion resistance of the resin.
着色剤としては、通常トナーに使用される染料及び顔料
等例えばカーボンブラック、ニグロシン、フタロシアニ
ンブルー、アニリンブルー メチレンブルー及びキノリ
ンイエロー等を使用することができる。As the colorant, dyes and pigments commonly used in toners, such as carbon black, nigrosine, phthalocyanine blue, aniline blue, methylene blue, and quinoline yellow, can be used.
さらに着色剤粒子の流動性、耐凝集性を向上させるため
、必要に応じて、例えばコロイド状シリカのような着色
粒子と同極性の疎水化されたコロイド状微粒子を添加す
ることもできる。Furthermore, in order to improve the fluidity and agglomeration resistance of the colorant particles, hydrophobized colloidal fine particles having the same polarity as the coloring particles, such as colloidal silica, may be added, if necessary.
着色−剤粒子の流動性の向上や帯電量の安定化のた、め
には、コロイド状シリカ以、外にも、酸化アルミ、ニウ
ム、酸化チタ・ン、酸化ケイ素、酸化亜鉛、酸、化マグ
ネシウム、酸化カルシウム、酸化スズ、酸化、インジウ
ム、酸化セリウム、−三酸化モリブデン等の無機・酸化
物、表面をシランカップリング剤、チタ′ンカップリ、
ング剤等のカップリング剤、シリコ、−ンオイル・等に
より表面も理された無機酸化物、ポリスチレン、スチレ
ン−ブタジェン共重合体、スチレン−アクリル共重合体
等のスチレン系共重合体、ポリエチレン及びエーチレラ
゛系共重合体、ポリメチルメタク、リレート等の脂肪−
族または脂環族共重合体、シリコーン樹脂、テ、フロン
等の樹脂微粉末〜表面をカッブリ、ング剤、シリコーン
オイル等で表面処理され・た樹脂微粉末、マグネタイト
、フェライト等、の磁性粉を添加しても良い。In order to improve the fluidity of colorant particles and stabilize the amount of charge, in addition to colloidal silica, aluminum oxide, nium oxide, titanium oxide, silicon oxide, zinc oxide, acids, and Inorganic and oxide materials such as magnesium, calcium oxide, tin oxide, indium, cerium oxide, and molybdenum trioxide, and silane coupling agents, titanium coupling agents,
Coupling agents such as coupling agents, inorganic oxides whose surfaces have been treated with silicone, oil, etc., styrenic copolymers such as polystyrene, styrene-butadiene copolymers, styrene-acrylic copolymers, polyethylene and ethereal Fats such as copolymers, polymethylmethac, rylates, etc.
Resin powders such as group or alicyclic copolymers, silicone resins, Te, Freon, etc. - Fine resin powders whose surfaces have been surface-treated with coating agents, silicone oil, etc., magnetic powders such as magnetite, ferrite, etc. May be added.
尚、本発明における着色粒子の帯電極性は正であっても
負であっても良い。Note that the charged polarity of the colored particles in the present invention may be positive or negative.
本発明の電子写真用トナーを得るためには、第1図に示
すように、核トナー2と、被覆トナー粒子1とを重量比
20:1で混練機例えばV型ブレンダー KRミキサー
OMタイザー等を用いて混練し、予備混合物10を得
た後、ハイブリタイザーまたはオングミル等により、造
粒処理を行うなどの方法が用いられる。このようにして
被覆トナー層3を有する電子写真用トナー11が得られ
る。また、上述のような機械的方法のほか、静電的、熱
的な方法を使用することもできる。In order to obtain the electrophotographic toner of the present invention, as shown in FIG. 1, the core toner 2 and the coated toner particles 1 are mixed in a weight ratio of 20:1 using a kneading machine such as a V-type blender, KR mixer, OM tizer, etc. After kneading to obtain the preliminary mixture 10, a method such as performing granulation treatment using a hybridizer, an ong mill, or the like is used. In this way, the electrophotographic toner 11 having the coated toner layer 3 is obtained. Furthermore, in addition to the mechanical method described above, electrostatic and thermal methods can also be used.
(作用)
トナー中に添加されたワックスは、加熱により即座に低
粘度の液状体となり、トナー表面にしみだしてトナーを
被覆し、定着ローラとトナーの離型性を高め、紙との接
着性を向上させる働きを有する。そのため、定着性の低
いトナー例えば耐摩耗性に優れた高融点のトナーであっ
ても、ワックスの添加により耐オフセット性及び被写体
への定着性が向上される。また、被覆トナー中のみにワ
ックスを混入することにより、ワックス量が少量ですみ
、高温時のトナーのケーキ化、流動性の悪化およびこれ
に伴う帯電性の低下、及び感光体上のフィルミング形成
等を防ぐことができる。(Function) When heated, the wax added to the toner instantly turns into a low-viscosity liquid, oozes out onto the toner surface, coats the toner, improves the releasability of the toner from the fixing roller, and improves the adhesion to the paper. It has the function of improving. Therefore, even if the toner has low fixing properties, such as a high melting point toner with excellent abrasion resistance, the anti-offset properties and the fixing properties to the subject can be improved by adding wax. In addition, by mixing wax only in the coated toner, the amount of wax can be reduced to a small amount, which prevents toner caking at high temperatures, deterioration of fluidity and accompanying decrease in chargeability, and formation of filming on the photoreceptor. etc. can be prevented.
(実施例) 以下、実施例を示し、本発明を具体的に説明する。(Example) EXAMPLES Hereinafter, the present invention will be specifically explained with reference to Examples.
実施例1
軟化点140℃、架橋タイプのスチレン−アクリル共重
合体樹脂(熱可塑性樹脂) 100重量部、カーボンブ
ラックMA−600(三菱化成側製−着色剤) 6重量
部及び5−34 (オリエント化学観製;染料)2重
量部を混合し、加圧ニーダを用いて約130℃にて30
分間混練した後、粗砕し、さらにI型ジェットミルDS
分級機(日本ニューマチック製)にて微粉砕し、風力分
級にて50%平均体積粒径8.0μmの核トナーを得た
。次に、スチレン−アクリル共重合体樹脂(架橋タイプ
) 100ffiffi部、低分子ポリブロピレン
ハイマー550P (工注化成■製;ワックス)50
重量部、カーボンブラックMA−600(三菱化成■製
) 6重量部及びS−34(オリエント化学■製)を混
合し、前記核トナーと同様にして混線、微粉砕を行い、
風力分級にて50%平均体積粒径3μmの被覆トナーを
得た。Example 1 Softening point: 140°C, 100 parts by weight of cross-linked styrene-acrylic copolymer resin (thermoplastic resin), 6 parts by weight of carbon black MA-600 (manufactured by Mitsubishi Kasei - colorant), and 5-34 (Orient) 2 parts by weight of chemical observation (dye) were mixed and heated at about 130°C for 30 minutes using a pressure kneader.
After kneading for a minute, it is coarsely crushed and further
It was finely pulverized using a classifier (manufactured by Nippon Pneumatic), and a core toner having a 50% average volume particle size of 8.0 μm was obtained by wind classification. Next, 100 ffiffi parts of styrene-acrylic copolymer resin (crosslinked type), 50 parts of low molecular weight polypropylene Hymer 550P (manufactured by Kochu Kasei; wax)
6 parts by weight of carbon black MA-600 (manufactured by Mitsubishi Kasei ■) and S-34 (manufactured by Orient Chemical ■) were mixed, mixed and finely pulverized in the same manner as the core toner,
A coated toner having a 50% average volume particle size of 3 μm was obtained by wind classification.
その後、核トナー及び被覆トナーを10=1の重量比で
V型ブレンダーを用いて60分間予予備台を行なった。Thereafter, the core toner and the coated toner were prepared in a weight ratio of 10=1 using a V-type blender for 60 minutes.
得られた予備混合物をホソカワミクロン型オングミルA
M−35でローター部回転数1800rpm、インナ一
部回転数700rpmの条件で融合、造粒処理を行い、
電子写真用トナーを得た。この電子写真用トナーを日本
鉄粉製フェライトキャリヤF−150とトナー比濃度4
%となるように混合し、現像剤を得た。The obtained premix was passed through a Hosokawa Micron type Ong Mill A.
Fusion and granulation were performed using M-35 under the conditions of a rotor rotation speed of 1800 rpm and an inner rotation speed of 700 rpm.
A toner for electrophotography was obtained. This electrophotographic toner was mixed with Nippon Iron Powder Ferrite Carrier F-150 and toner specific density 4.
% to obtain a developer.
得られた現像剤を使用し、画像評価試験を行なった。カ
ブリの発生及び画像濃度の低下は東芝製複写機レオドラ
イBD−9110を用い、20万枚連続複写後に評価し
た。その結果、カブリの発生及び画像濃度の低下は少な
く、良好な画像が得られた。定着性は複写画像上を荷重
をかけた布を往復させて擦り、その前後での画像濃度の
比を百分率で表した。その結果を第1表に示す。An image evaluation test was conducted using the obtained developer. The occurrence of fog and the decrease in image density were evaluated after continuous copying of 200,000 copies using a Toshiba Copying Machine RheoDry BD-9110. As a result, good images were obtained with little occurrence of fog or decrease in image density. The fixability was measured by rubbing a cloth under a load back and forth over the copied image, and expressing the ratio of image density before and after rubbing as a percentage. The results are shown in Table 1.
実施例2
実施例1で用いたものよりも分子量が高いスチレン−ア
クリル共重合体樹脂(軟化点 150℃)を用いる以外
は、実施例1と同様にして電子写真用トナーを得、これ
を用いて現像剤を得た。この現像剤を用い画像評価試験
を行なった。その結果を第1表に示す。Example 2 An electrophotographic toner was obtained in the same manner as in Example 1, except that a styrene-acrylic copolymer resin (softening point: 150°C) having a higher molecular weight than that used in Example 1 was used. A developer was obtained. An image evaluation test was conducted using this developer. The results are shown in Table 1.
比較例1
スチレン−アクリル共重合体樹脂(軟化点140℃ 架
橋タイプ) 100重量部、ハイマー550P 4
重量部、MA−6006重量部、5−34 2重量部を
混合し、加圧ニーダを用いて約130℃にて30分間混
練し、ハンマーミルにて50%平均体積粒径12.0μ
mとなるように微粉砕分級してトナーを得た。得られた
トナーを用いて現像剤を得、画像評価試験を行なった。Comparative Example 1 Styrene-acrylic copolymer resin (softening point 140°C, crosslinked type) 100 parts by weight, Hymer 550P 4
Parts by weight, parts by weight of MA-6006, and 2 parts by weight of 5-34 were mixed, kneaded for 30 minutes at about 130°C using a pressure kneader, and then 50% average volume particle size of 12.0μ using a hammer mill.
A toner was obtained by finely pulverizing and classifying the powder to give a particle size of m. A developer was obtained using the obtained toner, and an image evaluation test was conducted.
その結果を第1表に示す。The results are shown in Table 1.
比較例2
ワックス成分であるハイマー550Pを15重量部混合
する以外は、比較例1と同様にしてトナーを得た。得ら
れたトナーを用いて現像剤を得、画像評価試験を行なっ
た。その結果を第1表に示す。Comparative Example 2 A toner was obtained in the same manner as in Comparative Example 1, except that 15 parts by weight of Hymer 550P, which is a wax component, was mixed. A developer was obtained using the obtained toner, and an image evaluation test was conducted. The results are shown in Table 1.
尚、表中Oは良好、Δはやや不良、Xは不良であること
を示す。In the table, O indicates good, Δ indicates slightly poor, and X indicates poor.
表から明らかなように、本発明のトナーを用いると、カ
ブリのない良好な画像が得られ、定着性及びオフセット
温度の値も良好であるが、比較例1及び2に示すように
、ワックスを内添した場合は、定亡性が悪い。As is clear from the table, when the toner of the present invention is used, good images without fogging can be obtained, and the fixing properties and offset temperature values are also good. However, as shown in Comparative Examples 1 and 2, wax If it is attached internally, the stability of death is poor.
[発明の効果]
以上説明したように本発明によれば、ワックスを多量に
添加することにより生じる高温時のトナーのケーキ化、
流動性の悪化及びこれに伴う帯電性の低下、及び感光体
上のフィルミング形成等の弊害を最小限に押さえ、耐オ
フセット性に優れ、機械的な摩耗に強靭であり、かつ定
着性が良好な電子写真用トナーを提供することができる
。また、本発明のトナーを用いると、カブリが少なく鮮
明な転写画像が得られる。[Effects of the Invention] As explained above, according to the present invention, toner cake formation at high temperatures caused by adding a large amount of wax,
It minimizes adverse effects such as deterioration of fluidity and accompanying decrease in chargeability, and the formation of filming on the photoreceptor, and has excellent offset resistance, strong resistance to mechanical abrasion, and good fixing properties. It is possible to provide a toner for electrophotography. Further, when the toner of the present invention is used, a clear transferred image with less fog can be obtained.
第1図は、本発明の一実施例であるトナーの被覆工程を
示す図である。
1・・・被覆トナー粒子、2・・・核トナー 3・・・
被覆トナー層、10・・・予fr!混合物、11・・・
電子写真用トナーFIG. 1 is a diagram showing a toner coating process according to an embodiment of the present invention. 1... Coated toner particles, 2... Core toner 3...
Covering toner layer, 10...prefr! Mixture, 11...
Toner for electrophotography
Claims (1)
ーと、核トナー表面を被覆する該トナー成分及びワック
スを含む被覆トナーとを含有し、かつ前記ワックスが被
覆トナー中に1ないし80重量%含まれることを特徴と
する電子写真用トナー。A core toner containing a thermoplastic resin and a colorant as toner components, and a coated toner containing the toner components and wax that covers the surface of the core toner, and the wax is contained in the coated toner in an amount of 1 to 80% by weight. An electrophotographic toner characterized by:
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1262867A JPH03125156A (en) | 1989-10-11 | 1989-10-11 | Toner for electrophotograhy |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1262867A JPH03125156A (en) | 1989-10-11 | 1989-10-11 | Toner for electrophotograhy |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03125156A true JPH03125156A (en) | 1991-05-28 |
Family
ID=17381732
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1262867A Pending JPH03125156A (en) | 1989-10-11 | 1989-10-11 | Toner for electrophotograhy |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03125156A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5320926A (en) * | 1992-05-21 | 1994-06-14 | Kabushiki Kaisha Toshiba | Toner and method for manufacturing the same, and image forming apparatus using the toner |
JP2011232381A (en) * | 2010-04-23 | 2011-11-17 | Ricoh Co Ltd | Toner, developer, development apparatus, process cartridge and image formation apparatus |
WO2014148509A1 (en) * | 2013-03-19 | 2014-09-25 | 三菱化学株式会社 | Toner base particle and electrostatic image developing toner |
JP2015060141A (en) * | 2013-09-20 | 2015-03-30 | 京セラドキュメントソリューションズ株式会社 | Toner and manufacturing method of the same |
-
1989
- 1989-10-11 JP JP1262867A patent/JPH03125156A/en active Pending
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5320926A (en) * | 1992-05-21 | 1994-06-14 | Kabushiki Kaisha Toshiba | Toner and method for manufacturing the same, and image forming apparatus using the toner |
JP2011232381A (en) * | 2010-04-23 | 2011-11-17 | Ricoh Co Ltd | Toner, developer, development apparatus, process cartridge and image formation apparatus |
WO2014148509A1 (en) * | 2013-03-19 | 2014-09-25 | 三菱化学株式会社 | Toner base particle and electrostatic image developing toner |
JP2014209188A (en) * | 2013-03-19 | 2014-11-06 | 三菱化学株式会社 | Toner base particle and toner for electrostatic charge image development |
JP2015060141A (en) * | 2013-09-20 | 2015-03-30 | 京セラドキュメントソリューションズ株式会社 | Toner and manufacturing method of the same |
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