JPS6330857A - Dry toner - Google Patents
Dry tonerInfo
- Publication number
- JPS6330857A JPS6330857A JP61173561A JP17356186A JPS6330857A JP S6330857 A JPS6330857 A JP S6330857A JP 61173561 A JP61173561 A JP 61173561A JP 17356186 A JP17356186 A JP 17356186A JP S6330857 A JPS6330857 A JP S6330857A
- Authority
- JP
- Japan
- Prior art keywords
- toner
- melting point
- viscosity
- fixing
- normal temperature
- 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.)
- Granted
Links
- 239000011230 binding agent Substances 0.000 claims abstract description 19
- 238000002844 melting Methods 0.000 claims abstract description 16
- 230000008018 melting Effects 0.000 claims abstract description 16
- 239000000155 melt Substances 0.000 claims abstract description 7
- 150000002894 organic compounds Chemical class 0.000 claims abstract description 7
- 229920002545 silicone oil Polymers 0.000 abstract description 6
- 239000003795 chemical substances by application Substances 0.000 abstract description 5
- 239000003921 oil Substances 0.000 abstract description 2
- 238000001035 drying Methods 0.000 abstract 2
- 238000010008 shearing Methods 0.000 abstract 2
- 239000000463 material Substances 0.000 description 14
- 239000011347 resin Substances 0.000 description 11
- 229920005989 resin Polymers 0.000 description 11
- 238000000034 method Methods 0.000 description 9
- -1 I'1tn-butyl acrylate Chemical compound 0.000 description 5
- 239000001993 wax Substances 0.000 description 5
- 239000006229 carbon black Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000000049 pigment Substances 0.000 description 4
- 238000004898 kneading Methods 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 238000007639 printing Methods 0.000 description 3
- 238000010298 pulverizing process Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- DFYKHEXCUQCPEB-UHFFFAOYSA-N butyl 2-methylprop-2-enoate;styrene Chemical compound C=CC1=CC=CC=C1.CCCCOC(=O)C(C)=C DFYKHEXCUQCPEB-UHFFFAOYSA-N 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- KTZVZZJJVJQZHV-UHFFFAOYSA-N 1-chloro-4-ethenylbenzene Chemical compound ClC1=CC=C(C=C)C=C1 KTZVZZJJVJQZHV-UHFFFAOYSA-N 0.000 description 1
- OZCMOJQQLBXBKI-UHFFFAOYSA-N 1-ethenoxy-2-methylpropane Chemical compound CC(C)COC=C OZCMOJQQLBXBKI-UHFFFAOYSA-N 0.000 description 1
- RCSKFKICHQAKEZ-UHFFFAOYSA-N 1-ethenylindole Chemical compound C1=CC=C2N(C=C)C=CC2=C1 RCSKFKICHQAKEZ-UHFFFAOYSA-N 0.000 description 1
- CTXUTPWZJZHRJC-UHFFFAOYSA-N 1-ethenylpyrrole Chemical compound C=CN1C=CC=C1 CTXUTPWZJZHRJC-UHFFFAOYSA-N 0.000 description 1
- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 description 1
- WHBAYNMEIXUTJV-UHFFFAOYSA-N 2-chloroethyl prop-2-enoate Chemical compound ClCCOC(=O)C=C WHBAYNMEIXUTJV-UHFFFAOYSA-N 0.000 description 1
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 241000406668 Loxodonta cyclotis Species 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
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 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
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- SOGAXMICEFXMKE-UHFFFAOYSA-N alpha-Methyl-n-butyl acrylate Natural products CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- INLLPKCGLOXCIV-UHFFFAOYSA-N bromoethene Chemical compound BrC=C INLLPKCGLOXCIV-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- MEGHWIAOTJPCHQ-UHFFFAOYSA-N ethenyl butanoate Chemical compound CCCC(=O)OC=C MEGHWIAOTJPCHQ-UHFFFAOYSA-N 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 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
- 230000001747 exhibiting effect Effects 0.000 description 1
- XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical compound FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 description 1
- PBZROIMXDZTJDF-UHFFFAOYSA-N hepta-1,6-dien-4-one Chemical compound C=CCC(=O)CC=C PBZROIMXDZTJDF-UHFFFAOYSA-N 0.000 description 1
- 229920006158 high molecular weight polymer Polymers 0.000 description 1
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- AWJZTPWDQYFQPQ-UHFFFAOYSA-N methyl 2-chloroprop-2-enoate Chemical compound COC(=O)C(Cl)=C AWJZTPWDQYFQPQ-UHFFFAOYSA-N 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- 235000013872 montan acid ester Nutrition 0.000 description 1
- 239000012170 montan wax Substances 0.000 description 1
- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 description 1
- ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 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
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- WRAQQYDMVSCOTE-UHFFFAOYSA-N phenyl prop-2-enoate Chemical compound C=CC(=O)OC1=CC=CC=C1 WRAQQYDMVSCOTE-UHFFFAOYSA-N 0.000 description 1
- 108091008695 photoreceptors Proteins 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920005596 polymer binder Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 238000012546 transfer Methods 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
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/087—Binders for toner particles
- G03G9/08784—Macromolecular material not specially provided for in a single one of groups G03G9/08702 - G03G9/08775
- G03G9/08797—Macromolecular material not specially provided for in a single one of groups G03G9/08702 - G03G9/08775 characterised by their physical properties, e.g. viscosity, solubility, melting temperature, softening temperature, glass transition temperature
Landscapes
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- General Physics & Mathematics (AREA)
- Developing Agents For Electrophotography (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、電子写真法、静電記録法等において現像に用
いられる静電荷現像用トナー、更正こ詳しく言えば熱定
着用の乾式トナー1こ関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to an electrostatic charge developing toner used for development in electrophotography, electrostatic recording, etc. Regarding this.
電子写真法では感光体上fこ形成された静′f!Lm像
を通常顔料を含む樹脂粉で現像し、得られた可視画家を
転写紙上に転写して、熱、圧力及びその併用などにより
定着するが、この定着工程を高速かつ高効率に行なうこ
とが近年要求され、これらの点から熱ロール定着法が多
く採用されている。In electrophotography, a static image is formed on the photoreceptor. The Lm image is usually developed with resin powder containing pigment, and the resulting visible painter is transferred onto transfer paper and fixed using heat, pressure, or a combination thereof, but it is possible to perform this fixing process at high speed and with high efficiency. In recent years, the hot roll fixing method has been widely adopted due to these demands.
熱ロール定着法lこおいて、低消費電力で高速定着を行
なうためにはトナーの結着材料の軟化点を下げ、溶融粘
度を低下せしめることが有効な手段であるが、通常トナ
ーの主結着材料として用いられているバインダーポリマ
ー(結着樹脂)では、軟化点を下げるとトナー保管時に
ケーキングによる流動性の低下が生じゃ丁く、また溶融
粘度を下げると、オフセット現象などlこより、画家の
汚れが発生しや丁くなる。このため、熱ロールにシリコ
ンオイルなどの離型剤を供給する装置を設け、オフセッ
トを防止したり、また主バインダーポリマーのガラス転
移点を高くしたり、又はシリカなどの無機の超微粉をト
ナー表面への外添剤として用いて保管時のケーキングを
防ぐ方法が従来提案されでいる。In the hot roll fixing method, in order to perform high-speed fixing with low power consumption, it is effective to lower the softening point of the toner binder material and reduce the melt viscosity. When lowering the softening point of the binder polymer (binder resin) used as a bonding material, a decrease in fluidity due to caking occurs when toner is stored, and when the melt viscosity is lowered, offset phenomenon and other problems can occur. This will cause stains and stains. For this reason, a device is installed to supply a release agent such as silicone oil to the heated roll to prevent offset, and the glass transition point of the main binder polymer is increased, or ultrafine inorganic powder such as silica is added to the toner surface. A method of preventing caking during storage by using it as an external additive has been proposed.
しかし、熱ロールにシリコンオイルを供給するには、供
給機溝を必要とするため、装置のコストアップが必至で
あり、またオイル補給のメンテナンスも必要となる。However, supplying silicone oil to the heat roll requires a supply groove, which inevitably increases the cost of the device and requires maintenance for oil replenishment.
また主バインダーポリマーのガラス転移点を、高く設定
すると、軟化温度が高くなるために低温定着が困難とな
りや丁い。Furthermore, if the glass transition point of the main binder polymer is set high, the softening temperature will increase, making low-temperature fixing difficult.
またこれらに加えて、従来のトナーtこよる定着前まは
、樹脂の熱及び圧力による紙への付着固化を定着原理と
しているため、トナーの微粒化を行なわない限り、特に
高濃度部分は、画像の厚みが大きく、印刷に比べて不自
然な画像となりや丁い。In addition to these, since the conventional toner is fixed by adhering and solidifying the resin to the paper by heat and pressure before fixing, unless the toner is atomized, especially in high density areas, The image is too thick and looks unnatural compared to printing.
本発明は、熱定着用トナーにおける上記の問題点を改善
することを目的とする。An object of the present invention is to improve the above-mentioned problems in heat fixing toners.
すなわち、本発明の目的は、熱ロールにシリコンオイル
などの離型剤を供給しなくてもオフセット現象の発生し
ない乾式トナーを提供することにある。That is, an object of the present invention is to provide a dry toner that does not cause an offset phenomenon even if a release agent such as silicone oil is not supplied to a heated roll.
本発明の他の目的は、高速で効率よく定着を行なうこと
のできる乾式トナーを提供すること1こある。Another object of the present invention is to provide a dry toner that can be fixed efficiently at high speed.
さら(こ本発明の他の目的は、定着像の厚みが少なく、
印刷なみの自然さを有する良好な画像を形成しうる乾式
トナーを提供することにある。Furthermore, another object of the present invention is to reduce the thickness of the fixed image.
It is an object of the present invention to provide a dry toner capable of forming a good image having a naturalness similar to that of printing.
本発明は主結着剤として、常温以上の融点をもち、融点
より30°C以内の温度における溶融粘度が、せん断速
度102sec−”で10spoise以下の有機化合
物を使用した熱定着用乾式トナーを提供したものである
。The present invention provides a dry toner for heat fixing using, as a main binder, an organic compound having a melting point above room temperature and a melt viscosity of 10 spoise or less at a shear rate of 102 sec-'' at a temperature within 30°C of the melting point. This is what I did.
トナーの結着材料としては、従来高分子量の樹脂が用い
られ、混練法などにより、樹脂中にカーボンブラックの
ような顔料及び帯電制御剤などを混合し、微粉砕してト
ナーとしているが、この場合、結着樹脂は顔料等の要素
材料を保持固定化するとともに、定着に際しては熱及び
圧力またはその併用により、トナーが軟化し、紙表面の
凹凸ζこ沿って付着する機能を付与している。Conventionally, high-molecular-weight resins are used as binding materials for toners, and pigments such as carbon black and charge control agents are mixed into the resins using a kneading method, and the toners are made by finely pulverizing the resin. In this case, the binder resin holds and fixes elemental materials such as pigments, and during fixing, the toner is softened by heat and pressure, or a combination thereof, and has the function of adhering along the unevenness of the paper surface. .
熱ロール定着の場合、定着過程lこおいてトナーは通常
10’ poise以上の高粘度で流動するため、低内
部へのトナーの浸透は僅かでしかなく、過材1μ+ni
こも満たない。トナーの紙への定着度を決定する接着力
は紙表面での拡張による付着力の寄与が大きいと考えら
れる。この場合、紙の繊維内への浸透ζこよる効果はト
ナーの付着性の向上1こ、必ずしも充分活用されていな
い。In the case of hot roll fixing, during the fixing process the toner usually flows with a high viscosity of 10'poise or more, so the penetration of the toner into the inside is only small, and the overmaterial is 1μ+ni.
This is not enough. It is thought that the adhesive force that determines the degree of fixation of toner to paper is largely due to the adhesive force caused by expansion on the paper surface. In this case, the effect of penetration ζ into the paper fibers, which improves toner adhesion, is not necessarily fully utilized.
本発明の乾式トナーにおけるように溶融後の温度上昇下
で極めて低い粘度を示すような材料を結着樹脂として用
いると、トナーの紙繊維内部への浸透が期待され、トナ
ーと紙との間の接着面積を大幅(こ拡大でき、結果的に
比較的低温で、像強度の高い両1象が得られることIこ
なる。When a material that exhibits extremely low viscosity when the temperature rises after melting is used as the binder resin, as in the dry toner of the present invention, it is expected that the toner will penetrate into the paper fibers, and the gap between the toner and the paper will increase. The bonding area can be greatly expanded, and as a result, an image with high image strength can be obtained at a relatively low temperature.
高速の定着1こおいて、トナーの紙への浸透性を高める
にはトナーは熱ロールからの熱により、瞬時に溶解する
必要があり、実験的に融点より30°C以内の加熱で低
粘度化しうることが、必要条件であると判明した。For high-speed fixing 1, in order to improve the permeability of toner into paper, it is necessary for the toner to be instantly melted by the heat from the heated roll, and experimentally it has been shown that heating to within 30°C of the melting point can reduce the viscosity. It turns out that being able to transform is a necessary condition.
そしてその際の粘度は、通常のトナーの溶融粘度104
〜10’ poise (せん断速度10” 5ee−
” )よりはるかに低い103poise (せん断速
度102式−1)以下の材料を主結着剤としで含む場合
に、オフセットも少なく、浸透による接触面積拡大によ
る定着度の向上がみられる。この場合、定着度およびオ
フセットトナーtは、定着前の紙上の全トナー量に依存
するが、前記の物性を示す材料を用いた場合、充分な画
数a度と高速定着における充分な定着度が両立する。The viscosity at that time is the melt viscosity of normal toner, 104
~10' poise (shear rate 10" 5ee-
When the main binder contains a material with a shear rate of 103 poise (shear rate 102 formula-1), which is much lower than The degree of fixation and the offset toner t depend on the total amount of toner on the paper before fixing, but when a material exhibiting the above-mentioned physical properties is used, a sufficient number of strokes a degrees and a sufficient degree of fixation in high-speed fixing are both achieved.
また、融点の30℃以内という近傍で低粘度化すること
lこよって、定着画像の乱れ、オフセットを最少限(こ
押えることができる。Furthermore, by reducing the viscosity at a temperature within 30° C. of the melting point, disturbances and offsets in fixed images can be minimized.
熱ロールによるこのような加熱1こより瞬時lこ溶解し
、低粘変を示す有機化合物としては、ウレタンオリゴマ
ー、ポリエーテルオリゴマー、その他例えばスチレン、
パラクロルスチレンナトのスチレン類、ビニルナフタレ
ン、例えば塩化ビニル、臭化ビニル、フッ化ビニル、酢
酸ビニル、プロピオン酸ビニル、ベンジェ酸ビニル、酪
酸ビニルなどのビニルエステル類、例えばアクリル酸メ
チル、アクリル酸エチル、アクリルI’1tn−ブチル
、アクリル酸イソブチル、アクリル酸ドデシル、アクリ
ル酸n−オクチル、アクリル酸2−クロルエチル、アク
リル酸フェニル、α−クロルアクリル酸メチル、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
ルなどのメチレン脂肪族力ルボン酸エステル類、アクリ
ロニトリル、メタクリロニトリル、アクリルアミド、例
えばビニルメチルエーテル、ビニルイソブチルエーテル
、ビニルエチルエーテルなどのビニルエーテル類、例え
ばビニルメチルケトン、ビニルキシルケトンなどのビニ
ルケトン5、例えばN−ビニルピロール、N−ビニルカ
ルバゾール、N−ビニルインドール、N−ビニルピロリ
ドンなどのN−ビニル化合物などのビニル系モノマーの
ホモオリゴマーまたは他のモノマーとの共オリゴマーな
どのほか、カルナバワックス、モンタンワックス、パラ
フィンワックス、モンタン酸エステルワックス、アミド
ワックスなどの比較的硬度の高いワックス類、又はイン
シアネート化合物にアルコール類を付加反応した化合・
物などが単独又は混合して使用可能である。Examples of organic compounds that can be instantaneously dissolved by heating with a hot roll and exhibit low viscosity change include urethane oligomers, polyether oligomers, and others such as styrene,
Styrenes such as parachlorostyrene, vinylnaphthalene, vinyl esters such as vinyl chloride, vinyl bromide, vinyl fluoride, vinyl acetate, vinyl propionate, vinyl benzoate, vinyl butyrate, such as methyl acrylate, ethyl acrylate , I'1tn-butyl acrylate, isobutyl acrylate, dodecyl acrylate, n-octyl acrylate, 2-chloroethyl acrylate, phenyl acrylate, methyl α-chloroacrylate, methyl methacrylate, ethyl methacrylate, butyl methacrylate Methylene aliphatic carboxylic acid esters such as acrylonitrile, methacrylonitrile, acrylamide, vinyl ethers such as vinyl methyl ether, vinyl isobutyl ether, vinyl ethyl ether, vinyl ketones such as vinyl methyl ketone, vinyl xyl ketone, etc. In addition to homooligomers of vinyl monomers such as N-vinyl compounds such as N-vinylpyrrole, N-vinylcarbazole, N-vinylindole, and N-vinylpyrrolidone or co-oligomers with other monomers, carnauba wax and montan wax , relatively hard waxes such as paraffin wax, montanic acid ester wax, and amide wax, or compounds made by adding alcohols to incyanate compounds.
These substances can be used alone or in combination.
これらの有機化合物のうち、常温で硬度が高く、融点〜
融点+30℃の範囲において、溶融粘度がぜん断速度1
0” 5ee−1で10’ poise以下となるもの
であれば、いずれも用いることが可能である。分子量と
しては、比較的低分子量のもの、好ましくは5ooo以
下、より好ましくは2000以下のものがよく、かつ結
晶化度が高いものが好ましい。Among these organic compounds, they have high hardness at room temperature and have a melting point of ~
In the range of melting point +30℃, melt viscosity is shear rate 1
Any material can be used as long as it has a molecular weight of 10' poise or less at 0" 5ee-1. Regarding the molecular weight, one with a relatively low molecular weight, preferably 500 or less, more preferably 2000 or less. Those with good crystallinity and high crystallinity are preferred.
本発明(こよる乾式トナーは、溶融時に低粘変化すると
いう物性上の特徴があるので、熱ロール定着に限らず、
フラッシュ法、ラジアント法あるいはオーブン法などの
各柵の従来の熱定着法Iこも使用することかできる。The dry toner of the present invention has a physical characteristic of low viscosity change when melted, so it can be used not only for hot roll fixing but also for
Conventional heat fixing methods for each fence such as flash, radiant or oven methods may also be used.
本発明のトナーはこれらの瞬時溶解、低粘度型成分を結
着成分の主成分として多く含有するよう留意すれば副結
着材として、他の結着剤を併用することもできる。If care is taken to ensure that the toner of the present invention contains a large amount of these instant-dissolving, low-viscosity components as the main binder component, other binders may be used in combination as sub-binder materials.
副結着剤としては、先に述べたオリゴマーの原料モノマ
ーの高分子量重合体、すなわち従来バインダー樹脂とし
て用いられているものと同様の結着材を用いることがで
き、また同様に離型材としてポリエチレンワックス、ポ
リプロピレンワックスなどの併用もでき、また、着色剤
としては通常のカーボンブラックの他、種々の顔料、更
には磁性体を添加してもよい。As the secondary binder, a high molecular weight polymer of the raw material monomer of the oligomer mentioned above, that is, a binder similar to that conventionally used as a binder resin, can be used. Similarly, polyethylene can be used as a mold release material. Wax, polypropylene wax, etc. may be used in combination, and as colorants, in addition to ordinary carbon black, various pigments and even magnetic substances may be added.
ただし、これらの副結着樹脂または添加剤などの含有I
こより、溶l!lI粘度の著しい増加がないように留意
する必要がある。However, the content of these sub-binder resins or additives, etc.
From here, melt! Care must be taken to avoid a significant increase in lI viscosity.
以下、本発明の熱定着用乾式トナーを実施例により説明
する。なお下記の説明中、部は重量部を表わ丁。Hereinafter, the dry toner for heat fixing of the present invention will be explained with reference to Examples. In the following explanation, parts represent parts by weight.
実施例1
下記の表
1こ示す組成物を3本ロール混練(こより混合して、成
分A、Bの低粘性材料を得、この材料を用いて通常の混
練、粉砕法により下記の組成のトナーAおよびBを得た
。Example 1 The composition shown in Table 1 below was kneaded with three rolls to obtain a low-viscosity material of components A and B, and this material was used to make a toner with the following composition by ordinary kneading and pulverization methods. A and B were obtained.
トナーA:成分A70部、スチレン−n−ブチルメタク
リレート樹脂(Mn=12000. MW=50000
)15部、カーボンブラック(キャボットBPL)15
部。Toner A: 70 parts of component A, styrene-n-butyl methacrylate resin (Mn=12000. MW=50000
) 15 parts, carbon black (Cabot BPL) 15
Department.
トナーB:成分B 70部、他の成分はトナーAに同じ
。Toner B: 70 parts of component B, other components are the same as toner A.
平均粒径はトナ7A、Bとも11.0μmとし、フッ素
樹脂コートキャリアを用いて富士ゼロツク3500改造
機を用いて、複写を行ない、テフロンコートした熱ロー
ラーの温度を変えながら、定着試験を行なった。A、H
のトナーとも160℃以上で軽微なオフセットが見られ
たが、130℃(こおける定着度(li!lii象のウ
ェス摺擦テストによる)は、トナーBの万がAに比較し
て格段に丁ぐれていた。The average particle size was 11.0 μm for both toners 7A and B. Copying was performed using a modified Fuji Zerotsu 3500 machine using a fluororesin coated carrier, and a fixing test was conducted while changing the temperature of the Teflon-coated heat roller. . A, H
A slight offset was observed with both toners above 160°C, but the degree of fixation at 130°C (according to the li!lii elephant rag rubbing test) was much finer than that of toner A. They were separated.
また、A、Bのトナーを50℃にて1時間放置すること
によってケーキングテストを行なったところ、Aのトナ
ーはBのトナーに比較して多くの凝集がみられた。Further, when a caking test was conducted by leaving toners A and B at 50° C. for 1 hour, toner A showed more agglomeration than toner B.
実施例2
下記の組成
に示す組成物を3本ロール混線で混合し、成分D、Eの
低粘性材料を得、この材料り、Eを用いて常法の混練、
粉砕法により下記の組成のトナーDおよびトナーEを得
た。Example 2 The composition shown below was mixed using a three-roll mixer to obtain a low-viscosity material of components D and E. Using this material and E, kneading was carried out in a conventional manner.
Toner D and Toner E having the following compositions were obtained by the pulverization method.
トナーD:成分D60部、スチレン−n−ブチルメタク
リレート30部、カーボンブラック(キャボットBPL
)10部。Toner D: 60 parts of component D, 30 parts of styrene-n-butyl methacrylate, carbon black (Cabot BPL
) 10 copies.
トナーE:成分E60部、他の成分はトナーDと同様。Toner E: 60 parts of component E, other components are the same as toner D.
平均粒径はトナーD、Eとも11.5μとし、実施例1
と同様にして定着テストを実施した。The average particle size was 11.5μ for both toners D and E, and Example 1
A retention test was conducted in the same manner.
オフセントは、トナーDは170℃、Eは180℃以上
で 若干みられた。定着度は、130°Cで比較したと
ころトナーEがトナーDに比較して丁ぐれていた。実施
例1と同じ条件のケーキングテスト1こおいてもトナー
EがトナーDに比較して丁ぐれていた。Off-cent was slightly observed for toner D at 170°C and for toner E at 180°C or higher. When comparing the degree of fixation at 130°C, Toner E was inferior to Toner D. In the caking test 1 under the same conditions as in Example 1, Toner E was more crumbly than Toner D.
本発明の熱定着用乾式トナーは、常温では硬度が高く、
融点〜融点+30℃の温度範囲で急激lこ低粘度化する
有機化合物を主結着剤としたものであり、熱ロール定着
においてシリコンオイルなどの離型剤を用いなくともオ
フセット現象は発生せず、高速で効率よく定着を行なう
ことができ、定着像は厚みが少なく印刷なみの品質を示
す。The dry toner for heat fixing of the present invention has high hardness at room temperature;
The main binder is an organic compound whose viscosity decreases rapidly in the temperature range from melting point to melting point +30°C, and no offset phenomenon occurs even without the use of a release agent such as silicone oil during hot roll fixing. , fixing can be carried out efficiently at high speed, and the fixed image has a small thickness and has a quality comparable to that of printing.
Claims (1)
℃以内の温度における溶融粘度が、せん断速度10^2
sec^−^1で10^3poise以下の有機化合物
を使用したことを特徴とする熱定着用乾式トナー。As a main binder, it has a melting point above room temperature and 30° below the melting point.
The melt viscosity at a temperature within ℃ is the shear rate of 10^2
A dry toner for heat fixing, characterized in that an organic compound having a poise of 10^3 or less in sec^-^1 is used.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61173561A JPH083661B2 (en) | 1986-07-25 | 1986-07-25 | Dry toner |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61173561A JPH083661B2 (en) | 1986-07-25 | 1986-07-25 | Dry toner |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6330857A true JPS6330857A (en) | 1988-02-09 |
JPH083661B2 JPH083661B2 (en) | 1996-01-17 |
Family
ID=15962834
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61173561A Expired - Lifetime JPH083661B2 (en) | 1986-07-25 | 1986-07-25 | Dry toner |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH083661B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6358354A (en) * | 1986-08-29 | 1988-03-14 | Toyo Ink Mfg Co Ltd | Powdery toner |
JPS6366564A (en) * | 1986-09-09 | 1988-03-25 | Toyo Ink Mfg Co Ltd | Powdery toner |
JPH02190870A (en) * | 1989-01-20 | 1990-07-26 | Canon Inc | Thermal fixing method |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5821566A (en) * | 1981-07-31 | 1983-02-08 | Fuji Photo Film Co Ltd | Incubator |
JPS5879252A (en) * | 1981-11-06 | 1983-05-13 | Ricoh Co Ltd | Press fixable toner |
JPS59188658A (en) * | 1983-04-11 | 1984-10-26 | Canon Inc | Pressure fixable toner |
-
1986
- 1986-07-25 JP JP61173561A patent/JPH083661B2/en not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5821566A (en) * | 1981-07-31 | 1983-02-08 | Fuji Photo Film Co Ltd | Incubator |
JPS5879252A (en) * | 1981-11-06 | 1983-05-13 | Ricoh Co Ltd | Press fixable toner |
JPS59188658A (en) * | 1983-04-11 | 1984-10-26 | Canon Inc | Pressure fixable toner |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6358354A (en) * | 1986-08-29 | 1988-03-14 | Toyo Ink Mfg Co Ltd | Powdery toner |
JPS6366564A (en) * | 1986-09-09 | 1988-03-25 | Toyo Ink Mfg Co Ltd | Powdery toner |
JPH02190870A (en) * | 1989-01-20 | 1990-07-26 | Canon Inc | Thermal fixing method |
Also Published As
Publication number | Publication date |
---|---|
JPH083661B2 (en) | 1996-01-17 |
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