JPH0210387A - Image forming device - Google Patents
Image forming deviceInfo
- Publication number
- JPH0210387A JPH0210387A JP63159349A JP15934988A JPH0210387A JP H0210387 A JPH0210387 A JP H0210387A JP 63159349 A JP63159349 A JP 63159349A JP 15934988 A JP15934988 A JP 15934988A JP H0210387 A JPH0210387 A JP H0210387A
- Authority
- JP
- Japan
- Prior art keywords
- image
- transfer
- paper
- electric field
- toner
- 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
- 238000012546 transfer Methods 0.000 claims abstract description 64
- 238000000034 method Methods 0.000 claims abstract description 56
- 230000005684 electric field Effects 0.000 claims abstract description 25
- 239000000463 material Substances 0.000 claims abstract description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000011248 coating agent Substances 0.000 claims abstract description 6
- 238000000576 coating method Methods 0.000 claims abstract description 6
- 230000008569 process Effects 0.000 abstract description 12
- 238000004140 cleaning Methods 0.000 abstract description 9
- 238000004804 winding Methods 0.000 abstract description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 51
- 108091008695 photoreceptors Proteins 0.000 description 30
- 239000000377 silicon dioxide Substances 0.000 description 24
- 238000011161 development Methods 0.000 description 22
- 239000002245 particle Substances 0.000 description 21
- 229920002545 silicone oil Polymers 0.000 description 20
- 229920001577 copolymer Polymers 0.000 description 19
- 239000000843 powder Substances 0.000 description 17
- 230000005291 magnetic effect Effects 0.000 description 13
- 238000000926 separation method Methods 0.000 description 12
- 229920005989 resin Polymers 0.000 description 10
- 239000011347 resin Substances 0.000 description 10
- -1 chlorphenyl Chemical group 0.000 description 8
- 239000010419 fine particle Substances 0.000 description 8
- 238000009826 distribution Methods 0.000 description 7
- 230000003068 static effect Effects 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
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- 125000000217 alkyl group Chemical group 0.000 description 5
- 239000011162 core material Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 5
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 5
- 229910052782 aluminium Inorganic materials 0.000 description 4
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- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 230000005611 electricity Effects 0.000 description 3
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- 238000003379 elimination reaction Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- FFUAGWLWBBFQJT-UHFFFAOYSA-N hexamethyldisilazane Chemical compound C[Si](C)(C)N[Si](C)(C)C FFUAGWLWBBFQJT-UHFFFAOYSA-N 0.000 description 3
- 230000002209 hydrophobic effect Effects 0.000 description 3
- 239000006247 magnetic powder Substances 0.000 description 3
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- 239000000178 monomer Substances 0.000 description 3
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 3
- 229960004889 salicylic acid Drugs 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000001179 sorption measurement Methods 0.000 description 3
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical compound [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- CEGOLXSVJUTHNZ-UHFFFAOYSA-K aluminium tristearate Chemical compound [Al+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CEGOLXSVJUTHNZ-UHFFFAOYSA-K 0.000 description 2
- 229940063655 aluminum stearate Drugs 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000011230 binding agent Substances 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
- TUZBYYLVVXPEMA-UHFFFAOYSA-N butyl prop-2-enoate;styrene Chemical compound C=CC1=CC=CC=C1.CCCCOC(=O)C=C TUZBYYLVVXPEMA-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 229920003216 poly(methylphenylsiloxane) Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
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- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- 238000002834 transmittance Methods 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
- LNETULKMXZVUST-UHFFFAOYSA-N 1-naphthoic acid Chemical compound C1=CC=C2C(C(=O)O)=CC=CC2=C1 LNETULKMXZVUST-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- FEIQOMCWGDNMHM-UHFFFAOYSA-N 5-phenylpenta-2,4-dienoic acid Chemical compound OC(=O)C=CC=CC1=CC=CC=C1 FEIQOMCWGDNMHM-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000013032 Hydrocarbon resin Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229920007962 Styrene Methyl Methacrylate Polymers 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- FFCAWYKNBLTADM-UHFFFAOYSA-N butyl prop-2-enoate;2-ethylhexyl 2-methylprop-2-enoate;styrene Chemical compound C=CC1=CC=CC=C1.CCCCOC(=O)C=C.CCCCC(CC)COC(=O)C(C)=C FFCAWYKNBLTADM-UHFFFAOYSA-N 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 229940078456 calcium stearate Drugs 0.000 description 1
- LSFBQOPXRBJSSI-UHFFFAOYSA-L calcium;tetradecanoate Chemical compound [Ca+2].CCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCC([O-])=O LSFBQOPXRBJSSI-UHFFFAOYSA-L 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000002612 dispersion medium Substances 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000005294 ferromagnetic effect Effects 0.000 description 1
- 229910021485 fumed silica Inorganic materials 0.000 description 1
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 1
- 229920006270 hydrocarbon resin Polymers 0.000 description 1
- UCNNJGDEJXIUCC-UHFFFAOYSA-L hydroxy(oxo)iron;iron Chemical compound [Fe].O[Fe]=O.O[Fe]=O UCNNJGDEJXIUCC-UHFFFAOYSA-L 0.000 description 1
- 210000000936 intestine Anatomy 0.000 description 1
- 229910052742 iron 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
- 210000003127 knee Anatomy 0.000 description 1
- BJZBHTNKDCBDNQ-UHFFFAOYSA-L magnesium;dodecanoate Chemical compound [Mg+2].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O BJZBHTNKDCBDNQ-UHFFFAOYSA-L 0.000 description 1
- 239000000696 magnetic material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
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- ADFPJHOAARPYLP-UHFFFAOYSA-N methyl 2-methylprop-2-enoate;styrene Chemical compound COC(=O)C(C)=C.C=CC1=CC=CC=C1 ADFPJHOAARPYLP-UHFFFAOYSA-N 0.000 description 1
- 239000011859 microparticle Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
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- FJKIXWOMBXYWOQ-UHFFFAOYSA-N vinyl ethyl ether Natural products CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 1
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- 229940098697 zinc laurate Drugs 0.000 description 1
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- GPYYEEJOMCKTPR-UHFFFAOYSA-L zinc;dodecanoate Chemical compound [Zn+2].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O GPYYEEJOMCKTPR-UHFFFAOYSA-L 0.000 description 1
- GBFLQPIIIRJQLU-UHFFFAOYSA-L zinc;tetradecanoate Chemical compound [Zn+2].CCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCC([O-])=O GBFLQPIIIRJQLU-UHFFFAOYSA-L 0.000 description 1
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Landscapes
- Electrostatic Charge, Transfer And Separation In Electrography (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、負帯電性トナーと被膜性成分を含有する一成
分現像剤を使用する画像形成方法に関し、詳細には、静
電像相持体上のトナー画像を良好に転写材へ転写する工
程を有する画像形成方法に関する。Detailed Description of the Invention [Field of Industrial Application] The present invention relates to an image forming method using a monocomponent developer containing a negatively charged toner and a film-forming component. The present invention relates to an image forming method including a step of successfully transferring the above toner image to a transfer material.
[従来の技術]
従来、電子写真装置においては、非露光部に対して現像
を行なう正現像方法が一般的である。これは、原稿より
の反射光を光学処理した後に感光体上に投影される為、
反射光のない(原稿の文字部)非露光部に対し、現像を
行なうものである。[Prior Art] Conventionally, in electrophotographic apparatuses, a normal development method in which a non-exposed area is developed is generally used. This is because the reflected light from the original is optically processed and then projected onto the photoreceptor.
Development is performed on non-exposed areas (character areas of the original) where there is no reflected light.
最近、電子写真システムの用途が複写像を得る事以外に
、コンピューターの出力に用いられるプリンター等に用
いられるようになった。プリンタ用途の場合1発光体(
半導体レーザー等)が1画像値号に従ってオン−オフ(
ON−OFF)され、その光が感光体上に投影される。Recently, electrophotographic systems have come to be used not only for obtaining copied images but also for printers used for computer output. For printer use, one light emitter (
semiconductor laser, etc.) is turned on and off according to one image value number (
ON-OFF), and the light is projected onto the photoreceptor.
この際、通常、印字率(1頁当りの印字面積の割合)は
3割以下であり、文字部分に対して露光を行なう方式(
反転現像)が発光体寿命の点で優位である。At this time, the printing rate (ratio of printing area per page) is usually less than 30%, and the method of exposing the character part (
Reversal development) is advantageous in terms of luminescent life.
また、反転現像は、同一原稿より、ポジ画像およびネガ
画像を出力する様な装置(例えば、マイクロフィルム出
力装置)に用いられ、さらに同一装置内で、2色以上の
現像を行なう為に正現像および反転現像を組み合わせて
いる装置等に使用されるようになった。In addition, reversal development is used in devices that output positive images and negative images from the same document (for example, microfilm output devices), and in addition, in order to develop two or more colors in the same device, normal development is also used. It has come to be used in devices that combine reversal development and reversal development.
[発明が解決しようとする課題]
しかしながら、反転現像には次の様な問題点がある0通
常の現像(以下、正現像)における転写電界は、−次帯
電と同極性であり、画像担体(以下紙等)通過後、転写
電界が感光体上に印加されてもその影響は、イレース露
光(第1図中6)で消去される。[Problems to be Solved by the Invention] However, reversal development has the following problems. In normal development (hereinafter referred to as normal development), the transfer electric field has the same polarity as the negative charge, and the image carrier ( Even if a transfer electric field is applied to the photoreceptor after passing through the photoreceptor (hereinafter referred to as paper, etc.), its influence is erased by erase exposure (6 in FIG. 1).
一方、反転現像における転写電界は、−次帯電と反対極
性であり、紙等通過後も、転写電界を印加すると感光体
上に反対極性の帯電が起り、イレース露光では消去でき
ず1画像に濃淡となってあられれる。これは、「紙跡」
と称される現象である。On the other hand, the transfer electric field in reversal development has the opposite polarity to the -order charge, and even after passing through the paper, when the transfer electric field is applied, a charge of the opposite polarity occurs on the photoreceptor, which cannot be erased with erase exposure and only one image has shading. It will come to you. This is a "paper trail"
This is a phenomenon called.
紙跡対東としては、特開昭60−258173号公報に
見られる様に紙等が通過した後、転写電流を下げる等の
f段があるが、この方法は、種々の部品(マイクロスイ
ッチ等)が心安であり、装置が煩雑化するとどもに装置
原価が高くなる。また、転写電界を下げて感光体」二に
反対極性の帯電が起らない範囲にする手段が考えられる
。しかしながら、この方法では転写効率を下げる為、転
写不良に伴なう画質低下が起る。As for the paper trail, there is an f-stage that lowers the transfer current after the paper has passed, as seen in Japanese Patent Application Laid-Open No. 60-258173. ) is safe, and the more complicated the equipment, the higher the equipment cost. Another possible method is to lower the transfer electric field so that the photoreceptor is not charged with the opposite polarity. However, this method lowers the transfer efficiency, resulting in a reduction in image quality due to poor transfer.
反転現像法の他の弊害としては、感光体と紙等とが反対
極性に帯電されている為、強電界により帯電させた場合
に感光体と紙等とが、静電的に吸着し、転写工程終了後
も分離せず、次工程(クリーニング工程等)にまで1紙
等が入り込み紙詰り等を引起す、これは、「巻付」と称
される現象である3巻旧対策としては、特開昭56−6
0470号公報に見られる様に感光体と紙等との密着を
防ぐ手段がある。しかしながら、反転現像に於いて、こ
の方法は必ずしも有効ではない。すなわち、これは、反
転現像の転写工程の分離時における密着が、正現像方式
に較べ強い為と考えられる。別の方法としては米国特許
3,357,400明細書等に見られる様に、分離の補
助手段として、分離帯電またはベルト分離を具備する装
置がある。これにより、巻付現象に対しては効果がある
ものの、紙跡現象に対しては、効果はない、これは、分
離帯電は、転写帯電に較べて小さく、感光体」二の電位
にまで影響しない事による。Another problem with the reversal development method is that the photoreceptor and paper are charged with opposite polarities, so when charged with a strong electric field, the photoreceptor and paper will electrostatically attract each other, causing transfer problems. Even after the process is finished, the paper does not separate and gets into the next process (cleaning process, etc.), causing paper jams, etc. This is a phenomenon called "wrapping." Japanese Patent Publication No. 56-6
As seen in Japanese Patent No. 0470, there is a means to prevent the photoreceptor from coming into close contact with paper or the like. However, this method is not necessarily effective in reversal development. That is, this is considered to be because the close contact during separation in the transfer process of reversal development is stronger than that of normal development. Another method, as seen in U.S. Pat. No. 3,357,400, is an apparatus that includes separate charging or belt separation as an auxiliary means for separation. Although this is effective against the wrapping phenomenon, it is not effective against the paper trail phenomenon. This is because the separation charge is smaller than the transfer charge, and it even affects the potential of the photoreceptor. Depends on what you don't do.
別の手段としては、転写電界を下げて静電吸着力を下げ
る手段があるが、この方法は、前述のように転写不良に
伴う画質低下が起こりやすい、また、転写電界を下げる
と、転写効率の低下が起り、転写に不利なハガキ、01
(P用フィルム等の多様なニーズに答えられない。また
転写電界を下げると、画像の輪郭部分、線画部分の如き
、現像剤が集中しやすい部分(エッヂ現像部分)で、転
写不良の一部である「転写なか抜け」が起る。これは、
エッヂ現像部は通常部に較べ現像剤が多くのり、現像剤
凝集が起りやすく、転写電界に対する応答が下がる為と
考えられ、そのため、Wl像に忠実である高品位な画像
を得るのが困難になるという問題点を有している。Another method is to reduce the electrostatic attraction force by lowering the transfer electric field, but as mentioned above, this method is likely to cause a reduction in image quality due to poor transfer. Postcards that are disadvantageous for transcription due to a decrease in 01
(Unable to meet the diverse needs of P films, etc.) Also, if the transfer electric field is lowered, some transfer defects may occur in areas where developer tends to concentrate (edge development areas), such as image outlines and line drawing areas. ``transcription omission'' occurs.This is,
This is thought to be due to the fact that more developer is deposited in the edge development area than in the normal area, and developer aggregation is more likely to occur, resulting in a lower response to the transfer electric field.As a result, it is difficult to obtain a high-quality image that is faithful to the Wl image. It has the problem of becoming.
本発明の目的は、上述の問題点を解決した画像形成方法
を提供することにある。An object of the present invention is to provide an image forming method that solves the above-mentioned problems.
本発明の目的は、反転現像方法のような低転写電界によ
る転写が心穴な画像形成方法において、転写担体の条件
によらず、潜像に忠実である高品位な画像が得られる転
写工程を有する画像形成方法を提供することにある。An object of the present invention is to provide a transfer process that can obtain high-quality images that are faithful to the latent image, regardless of the conditions of the transfer carrier, in image forming methods such as reversal development methods, where transfer using a low transfer electric field is a drawback. An object of the present invention is to provide an image forming method having the following features.
本発明の目的は、「紙跡」、「巻付」、「転写なか抜け
」等の現象がないか、または、該現象が抑制されている
画像形成方法を提供することにある。An object of the present invention is to provide an image forming method in which phenomena such as "paper marks,""wrapping," and "transfer missing" are free or suppressed.
本発明の目的は反転現像装置におけるような、低転写電
界ドにおいても中抜は現象を起こさず、耐久性が良好な
画像形成方法を提供することにある。SUMMARY OF THE INVENTION An object of the present invention is to provide an image forming method that does not cause hollowing even in a low transfer electric field such as in a reversal developing device and has good durability.
[課題を解決するための手段]
本発明は、」二記目的を達成するためになされたもので
、静電荷像保持体上の静電荷像を一成分系現像剤で現像
し、静電荷像保持体上に形成された現像剤画像を転写材
へ静電転写する画像形成方法においで、水との接触角が
80%以上の滑性面を前記保持体表面に形成させる被膜
性物質を0.u〜!、0重量部(対トナー100重量部
)含有する一成分系現像剤を使用し、一次帯電電界Vp
rと転写帯電電界Vtrとの比(V tr/ V pr
)が負となる条件下及び(V t r/ V p r)
の絶対値が0.5乃至1.6である条件下で、トナー画
像を静電転写することを特徴とするものである。[Means for Solving the Problems] The present invention has been made to achieve the second object, and is to develop an electrostatic image on an electrostatic image carrier with a one-component developer, In an image forming method in which a developer image formed on a holder is electrostatically transferred to a transfer material, a coating substance that forms a slippery surface with a contact angle with water of 80% or more on the surface of the holder is used. .. U~! , 0 parts by weight (100 parts by weight of toner) is used, and the primary charging electric field Vp
The ratio of r to the transfer charging electric field Vtr (V tr/V pr
) is negative and (V tr/V p r)
The method is characterized in that a toner image is electrostatically transferred under conditions where the absolute value of is 0.5 to 1.6.
本発明の画像形成方法に使用される被膜性物質としては
、次式で表わされるシリコンオイルR:炭素数1〜3の
アルキル基
R′:アルキル、ハロゲン変性アルキル。The film-forming substance used in the image forming method of the present invention is silicone oil represented by the following formula: R: Alkyl group having 1 to 3 carbon atoms R': Alkyl, halogen-modified alkyl.
フェニル、変性フェニル等のシリコ
ンオイル変性基
R“:炭素数1〜3のアルキル基又はアルコキシ基
m:5〜100の整数
n二〇〜50の整数
であって、例えば、ジメチルシリコンオイル、アルキル
変性シリコンオイル、α−メチルスチレン変性シリコン
オイル、クロルフェニルシリコンオイル、フッ素変性シ
リコンオイル等が挙げられる。Silicone oil modified group R" such as phenyl and modified phenyl: Alkyl group or alkoxy group having 1 to 3 carbon atoms m: An integer from 5 to 100 n An integer from 20 to 50, such as dimethyl silicone oil, alkyl modified Examples include silicone oil, α-methylstyrene-modified silicone oil, chlorphenyl silicone oil, fluorine-modified silicone oil, and the like.
また、次式で表わされる脂肪酸金属セッケン(R−G−
0)nM
R:炭素数10〜20の脂肪族若しくは不飽和脂肪族
n:l〜3の整数
M:価数1〜3の金属
であって、例えばステアリン酸亜鉛、ラウリル酸亜鉛、
ミリスチン酸亜鉛、ステアリン酸カルシウム、ステアリ
ン酸アルミニウム等が挙げられる。In addition, fatty acid metal soap (R-G-
0) nM R: aliphatic or unsaturated aliphatic having 10 to 20 carbon atoms n: an integer of 1 to 3 M: a metal with a valence of 1 to 3, such as zinc stearate, zinc laurate,
Examples include zinc myristate, calcium stearate, and aluminum stearate.
以上、被膜性物質の例を挙げたが、これらに限定される
ものではない。Although examples of film-forming substances have been given above, the present invention is not limited to these.
静電荷像保持体表面の水との接触角は次のように測定す
る。協和接触角計GA−O9を用い、サンプル表面が直
統鏡より見て水平になるように取付ける0表面にイオン
交換処理を施した純水104gを滴下する。直続鏡から
1/2 θを測定し、これより接触角θを求める。被膜
形成は、主としてクリーニング工程により行なわれてい
ると考えられる。The contact angle of the surface of the electrostatic image carrier with water is measured as follows. Using a Kyowa contact angle meter GA-O9, 104 g of ion-exchanged pure water was dropped onto the surface of the sample, which was attached so that the sample surface was horizontal when viewed from a direct mirror. 1/2 θ is measured from the straight mirror, and the contact angle θ is determined from this. It is thought that film formation is mainly carried out by the cleaning process.
つまり静電荷像保持体上へは現像剤と共に移動し転写せ
ずに残った被膜性物質が、クリーニング工程での機械的
な作用により、ヘキ壊もしくは延伸されることで保持体
上に撥水性の被膜を形成させる。In other words, the coating material that moves with the developer and remains untransferred onto the electrostatic charge image carrier is cracked or stretched by the mechanical action during the cleaning process, resulting in a water-repellent coating on the carrier. Form a film.
被膜性物質の添加量は、トナー100重量部に対し0、
O1〜1.0重量部である事が好ましい、 0.01重
量部以下では添加効果が認められず転写に関する問題が
起る。また、1.0重量部以上では現像剤担体等の部分
に対し、被膜形成が起り現像に関する問題が起る。特に
好ましくは0.03〜0.5重量部である。The amount of film substance added is 0 to 100 parts by weight of toner.
It is preferable that the amount of O is 1 to 1.0 parts by weight. If it is less than 0.01 parts by weight, no effect will be observed and problems related to transfer will occur. Moreover, if it exceeds 1.0 parts by weight, a film will be formed on parts such as the developer carrier, causing problems regarding development. Particularly preferably 0.03 to 0.5 parts by weight.
本発明に用いられる被膜性物質は、現像剤と共に挙動し
ていることを特徴としている。これは、特開昭56−1
30470号公報における非画像に粒子を積極的に配し
て転写材と感光体間−の吸着力を下げる方法とは全く異
なるものである。The film material used in the present invention is characterized by behaving together with the developer. This is JP-A-56-1
This method is completely different from the method disclosed in Japanese Patent No. 30470, in which particles are actively placed on non-image areas to reduce the adsorption force between the transfer material and the photoreceptor.
特開昭5fl−Et0470号公報の方法によれば、転
写電界を下げることなく巻付現象を改善できるが1紙跡
現象に対しては効果がなく、また低転写電界下で転写率
を向上させる効果もないものである。According to the method disclosed in Japanese Patent Application Laid-Open No. 5fl-Et0470, the wrapping phenomenon can be improved without lowering the transfer electric field, but it is not effective against the single paper mark phenomenon, and the transfer rate can be improved under a low transfer electric field. It has no effect.
本発明に用いる転写工程としてはコロナ放電帯電器、当
接ローラー帯電器等により発生する′電界を用いる静電
転写方式が挙げられる。転写の条件は次のように測定す
る。添付図面の第1図を参照しながら説明すると、画像
形成装置からクリーニング装M8.現像器9.転写帯電
器3等を取りはずし、静電像保持体である感光体(感光
ドラム)1を、−成帯電器2で帯電させる。漏れ光を、
実質的に完全に遮光して感光体1の1周分を帯電させた
後に、感光体の表面電位を表面電位計で測定する。この
時の表面電位の値をvpr[vlとする0次に、感光体
表面をアルコールを含浸した布等で拭いて、感光体表面
を除電した後、−次帯電器2を取り外し、転写帯電器3
を取り付けて、感光体lの1周分を帯電させた後に、感
光体の表面電位を測定する。この時の表面電位の値をV
tr[V]とする1本発明においてV tr/ V p
rの値0.5〜1.6である。該絶対値が0.5未満の
場合は、転写電界が低すぎて、転写時に画像劣化が起こ
りやすく、−勇猛絶対値が1.6を越えると、転写電界
が強すぎて、感光体が正に帯電しやすく、紙跡現象およ
び巻付現象が発生しやすくなる。The transfer process used in the present invention includes an electrostatic transfer method using an electric field generated by a corona discharge charger, a contact roller charger, or the like. Transfer conditions are measured as follows. Referring to FIG. 1 of the accompanying drawings, the cleaning device M8. Developing device9. The transfer charger 3 and the like are removed, and the photoreceptor (photosensitive drum) 1, which is an electrostatic image holder, is charged with the negative charger 2. leaked light,
After substantially completely blocking light and charging the photoreceptor 1 for one revolution, the surface potential of the photoreceptor 1 is measured with a surface electrometer. The value of the surface potential at this time is vpr[vl.0 Next, after removing the charge from the photoreceptor surface by wiping the surface of the photoreceptor with a cloth impregnated with alcohol, remove the -order charger 2, and remove the transfer charger. 3
After charging the photoreceptor l for one revolution, the surface potential of the photoreceptor is measured. The value of the surface potential at this time is V
tr[V] In the present invention, V tr/V p
The value of r is 0.5 to 1.6. If the absolute value is less than 0.5, the transfer electric field is too low and image deterioration is likely to occur during transfer; if the absolute value exceeds 1.6, the transfer electric field is too strong and the photoreceptor is It is easy to be charged with electricity, and paper trail phenomenon and wrapping phenomenon tend to occur.
1.4である。It is 1.4.
本発明は、有機感光体(以下OPC感光体)を用いる画
像形成方法(装置)に対し有効であり、OPC感光体が
電荷発生層および電荷輸送層を少なくとも有する多層に
より構成されている積層型OPCを使用する反転現像方
式の画像形成方法に対し、特に有効である。ape感光
体では、感光層が逆極性に帯電した場合、電荷の動きが
鈍く、特に積層型OPCでは、この傾向が顕著になり、
紙跡が発生17やすいことから、本発明は特に効果を発
揮する。The present invention is effective for an image forming method (apparatus) using an organic photoreceptor (hereinafter referred to as an OPC photoreceptor), and the OPC photoreceptor is a multilayer OPC formed of a multilayer structure having at least a charge generation layer and a charge transport layer. This is particularly effective for image forming methods using reversal development methods. In the APE photoreceptor, when the photosensitive layer is charged to the opposite polarity, the charge movement is slow, and this tendency is particularly noticeable in laminated OPCs.
The present invention is particularly effective since paper marks are likely to occur17.
本発明に用いるV、rの値としては、−300〜−i、
ooorv ]が好マシく、4Sニー5oo 〜−90
0[V]が好ましい、−300[V]未満では現像時の
電位差を確保することが困難であり、画像が不鮮明とな
りやすく、一方−1,000[V]を越える場合は、電
界による感光層の絶縁破壊が起り、黒ポチ等の画質劣化
が起りやすい、耐久性等より、−500〜−900[V
]が特に好ましい。The values of V and r used in the present invention are -300 to -i,
ooorv ] is better, 4S knee 5oo ~ -90
0 [V] is preferable. If it is less than -300 [V], it is difficult to secure a potential difference during development and the image tends to become unclear. On the other hand, if it exceeds -1,000 [V], the photosensitive layer due to the electric field -500 to -900 [V
] is particularly preferred.
本発明の画像形成方法は、機械的分離手段を使用せずに
、転写材(紙等)の弾性力、感光体の曲率、除電ブラシ
等により、転写材を感光体から分離する1画像形成方法
(装置)に対して特に有効である。機械的分離機構を持
たない装置での分離状態は、転写条件に依存しており、
巻付があられれやすいので、本発明は特に効果を発揮す
る。The image forming method of the present invention is an image forming method in which a transfer material is separated from a photoreceptor using the elastic force of the transfer material (paper, etc.), the curvature of the photoreceptor, a static elimination brush, etc., without using mechanical separation means. It is particularly effective against (devices). The separation state in devices that do not have a mechanical separation mechanism depends on the transfer conditions.
The present invention is particularly effective because the windings are prone to cracking.
本発明は感光体lの直径(第1図中の「φ」)が50鳳
請以下の感光体を使用する画像形成方法(装置)に、特
に有効である。φ50mm以下の感光ドラムが使用され
る装置では、小型化を意図しており、部品点数も少なく
する必要があり、通常、分離工程は紙の弾性力のみによ
る分離および除電ブラシ7等により構成されている(第
2図参照)。The present invention is particularly effective in an image forming method (apparatus) using a photoreceptor having a diameter ("φ" in FIG. 1) of 50 mm or less. Devices that use photosensitive drums with a diameter of 50 mm or less are intended to be miniaturized, and the number of parts must be reduced. Usually, the separation process consists of separation using only the elastic force of paper and a static elimination brush 7, etc. (See Figure 2).
この際、除電工程は、紙等のみの除電を行なっており、
通常、感光体の表面電位に対しては、作用しない。At this time, the static electricity removal process only removes static electricity from paper, etc.
Usually, it does not affect the surface potential of the photoreceptor.
第1図を参照しながら、画像形成工程を説明する。−成
帯電器2で感光体表面を負極性に帯電し、光源またはレ
ーザー光による露光5によりイメージスキャニングによ
りH!i像を形成し、磁性ブレード11および磁石を内
包している現像スリーブ4を具備する現像器9で一成分
系磁性現像剤13で該潜像を反転現像する。現像部にお
いて感光ドラム1と現像スリーブ4との間で、バイアス
印加手段によりバイアスが印加されている。転写紙Pが
搬送されて、転写部にくると転写帯電器3により転写紙
Pの背面(感光ドラム側と反対面)から正極性の帯電を
することにより感光ドラム表面上の負荷電性トナー像が
転写紙P上へ静電転写される。転写帯11を器3を通過
直後に、除電ブラシエ0により転写紙背面の電荷を除電
しつつ、転写紙Pを感光ドラム1から曲率分離により分
離する0曲率分離によって感光ドラムlから分離された
転写紙Pは、加熱加圧ローラ定着器7により転写紙P上
のトナー画像は、定着される。The image forming process will be explained with reference to FIG. - Charge the surface of the photoreceptor to negative polarity with the charger 2, and perform H! by image scanning with exposure 5 using a light source or laser light. An i-image is formed, and the latent image is reversely developed using a one-component magnetic developer 13 in a developing device 9 equipped with a magnetic blade 11 and a developing sleeve 4 containing a magnet. In the developing section, a bias is applied between the photosensitive drum 1 and the developing sleeve 4 by a bias applying means. When the transfer paper P is conveyed and reaches the transfer section, the transfer charger 3 charges the transfer paper P with positive polarity from the back side (the opposite side to the photosensitive drum side), thereby forming a negatively charged toner image on the surface of the photosensitive drum. is electrostatically transferred onto the transfer paper P. Immediately after the transfer band 11 passes through the device 3, the transfer paper P is separated from the photosensitive drum 1 by curvature separation while eliminating the charge on the back side of the transfer paper by the static eliminating brush 0. Transfer separated from the photosensitive drum L by 0 curvature separation. The toner image on the transfer paper P is fixed by the heating and pressure roller fixing device 7 .
また、転写工程後の感光ドラムに残留する一成分系現像
剤は、クリーニングブレードを有するクリーニング器8
で除去される。クリーニング後の感光ドラム1は、イレ
ース露光6により除電され、再度、−成帯電器2による
帯電工程から始まる工程が繰り返される0次に、本発明
で使用される負荷電性トナーに関して述べる。Further, the one-component developer remaining on the photosensitive drum after the transfer process is removed by a cleaning device having a cleaning blade.
will be removed. After cleaning, the photosensitive drum 1 is neutralized by erase exposure 6, and the steps starting from the charging step by the negative charger 2 are repeated again.Next, the negatively charged toner used in the present invention will be described.
本発明においてトナーの結着樹脂としては、例えば、ポ
リスチレン、ポリ−p−クロルスチレン。In the present invention, examples of the binder resin for the toner include polystyrene and poly-p-chlorostyrene.
ポリビニルトルエンなどのスチレンおよびその置換体の
単重合体;スチレン−p−クロルスチレン共重合体、ス
チレン−プロピレン共重合体、スチレン−ビニルトルエ
ン共重合体、スチレン−ビニルナフタリン共重合体、ス
チレン−アクリル酸メチル共重合体、スチレンーアクリ
ル酸エチル共重合体、スチレン−アクリル酸ブチル共重
合体、スチレン−アクリル酸オクチル共重合体、スチレ
ン−メタアクリル酸メチル共重合体、スチレン−メタア
クリル酸エチル共重合体、スチレン−メタアクリル酸ブ
チル共重合体、スチレン−α−クロルメタアクリル酸メ
チル共重合体、スチレン−アクリロニトリル共重合体、
スチレン−ビニルメチルエーテル共重合体、スチレン−
ビニルエチルエーテル共重合体、スチレン−ビニルメチ
ルケトン共重合体、スチレン−ブタジェン共重合体、ス
チレン−イソプレン共重合体、スチレン−アクリロニト
リル−インデン共重合体などのスチレン系共重合体;ポ
リ塩化ビニル、ポリ酢酸ビニル、ポリエチレン、ポリプ
ロピレン、シリコーン樹脂、ポリエステル、エポキシ樹
脂、ポリビニルブチラール、ロジン、変性ロジン、テル
ペン樹脂、フェノール樹脂、キシレン樹脂、脂肪族又は
脂環族炭化水素樹脂、芳香族系石油樹脂、塩素化パラフ
ィン、パラフィンワックスなどが、単独或いは混合して
用いられる。Monopolymers of styrene and its substituted products such as polyvinyltoluene; styrene-p-chlorostyrene copolymer, styrene-propylene copolymer, styrene-vinyltoluene copolymer, styrene-vinylnaphthalene copolymer, styrene-acrylic acid methyl copolymer, styrene-ethyl acrylate copolymer, styrene-butyl acrylate copolymer, styrene-octyl acrylate copolymer, styrene-methyl methacrylate copolymer, styrene-ethyl methacrylate copolymer Polymer, styrene-butyl methacrylate copolymer, styrene-α-methyl chloromethacrylate copolymer, styrene-acrylonitrile copolymer,
Styrene-vinyl methyl ether copolymer, styrene-
Styrenic copolymers such as vinyl ethyl ether copolymer, styrene-vinyl methyl ketone copolymer, styrene-butadiene copolymer, styrene-isoprene copolymer, styrene-acrylonitrile-indene copolymer; polyvinyl chloride, Polyvinyl acetate, polyethylene, polypropylene, silicone resin, polyester, epoxy resin, polyvinyl butyral, rosin, modified rosin, terpene resin, phenolic resin, xylene resin, aliphatic or alicyclic hydrocarbon resin, aromatic petroleum resin, chlorine Chemical paraffin, paraffin wax, etc. may be used alone or in combination.
本発明においては、これらの樹脂の中でも、スチレン−
アクリル系共重合体が好ましく用いられ、特にスチレン
−アクリル酸n−ブチル(St−nBA)共重合体、ス
チレン−メタアクリル酸n−ブチル(St−nBMA)
共重合体、スチレン−アクリル酸n−ブチル−メタアク
リル酸2−エチルヘキシル(St−nBA−2EHMA
)共重合体等が好ましく用いられる。In the present invention, among these resins, styrene-
Acrylic copolymers are preferably used, particularly styrene-n-butyl acrylate (St-nBA) copolymer and styrene-n-butyl methacrylate (St-nBMA).
Copolymer, styrene-n-butyl acrylate-2-ethylhexyl methacrylate (St-nBA-2EHMA
) copolymers etc. are preferably used.
また、本発明に係るトナーに添加し得る着色材料として
は、従来公知のカーボンブラック、銅フタロシアニン、
鉄黒などが使用できる。Further, as coloring materials that can be added to the toner according to the present invention, conventionally known carbon black, copper phthalocyanine,
Iron black etc. can be used.
本発明に係る磁性トナーに含有される磁性微粒子として
は、磁場の中に置かれて磁化される物質が用いられ、鉄
、コバルト、ニッケルなどの強磁性金属の粉末もしくは
マグネタイト、γ−Fe2O3゜フェライトなどの合金
や化合物が使用できる。As the magnetic fine particles contained in the magnetic toner of the present invention, a substance that is magnetized by being placed in a magnetic field is used, such as powder of a ferromagnetic metal such as iron, cobalt, or nickel, or magnetite, γ-Fe2O3° ferrite. Alloys and compounds such as can be used.
これらの磁性微粒子は窒素吸着法によるBET比表面積
が好ましくは2〜20m27g、特に2.5〜12鳳2
7g、さらにモース硬度が5〜7の磁性粉が好ましい、
この磁性粉の含有量は、トナー量に対して10〜70重
量%が良い。These magnetic fine particles preferably have a BET specific surface area of 2 to 20 m27g, particularly 2.5 to 12g, determined by the nitrogen adsorption method.
7g, preferably magnetic powder with a Mohs hardness of 5 to 7.
The content of this magnetic powder is preferably 10 to 70% by weight based on the amount of toner.
また、本発明のトナーには必要に応じて荷電制御剤を含
有しても良く、モノアゾ染料の金属錯塩;サリチル酸、
アルキルサリチル酸、ジアルキルサリチル酸またはナフ
トエ酸の金属錯塩等の負荷電制御剤が用いられる。Further, the toner of the present invention may contain a charge control agent if necessary, such as a metal complex salt of a monoazo dye; salicylic acid;
A negative charge control agent such as a metal complex salt of alkyl salicylic acid, dialkyl salicylic acid or naphthoic acid is used.
さらに、本発明に係る磁性トナーは体積固有抵抗が10
1OΩ・cm以上、特に1012Ω・C■以上であるの
がトリポ電荷および静電転写性の点で好ましい、ここで
言う体積固有抵抗は、トナーを100kg/cm2 ノ
圧で成型し、コレニt00V/cm c7)電界を印加
して、印加後1分を経た後の電流値から換算した値とし
て定義される。Furthermore, the magnetic toner according to the present invention has a volume resistivity of 10
It is preferable that it is 10Ω・cm or more, especially 1012Ω・C■ or more in terms of tripod charge and electrostatic transferability. c7) Defined as a value calculated from the current value after 1 minute has passed after applying an electric field.
本発明に使用される負帯電性磁性トナーのトリポ電荷量
は−8gc/g乃至−20pc/gを有する必要がある
。 −8gc/gに満たない場合は画像濃度が低い傾向
にあり、特に高湿下での影響が著しい、また− 20p
c/gを越えると、トナーのチャージが高過ぎてライン
画像等が細く特に低湿下で貧弱な画像となる。The negatively charged magnetic toner used in the present invention must have a tripocharge amount of -8 gc/g to -20 pc/g. If it is less than -8gc/g, the image density tends to be low, and the effect is particularly noticeable under high humidity, and -20p
If it exceeds c/g, the toner charge will be too high, resulting in thin line images and poor images especially under low humidity.
本発明の負帯電性トナー粒子とは、25℃、50〜60
%RHの環境下に1晩放置され−たトナー粒子10gと
200〜300メツシユに主体粒度を持つ、樹脂で被覆
されていないキャリアー鉄粉(例えば、日本鉄粉社製E
FV200/300) 90 gとを前記環境下でおよ
そ200c、c、の容積を持つアルミニウム製ポット中
で充分に(手で持って上下におよそ50回振とうする)
混合し、400メツシユスクリーンを有するアルミニウ
ム製のセルを用いて通常のブローオフ法により、トナー
粒子のトリポ電荷量を測定する。The negatively charged toner particles of the present invention are 25°C, 50 to 60°C.
% RH overnight - 10 g of toner particles and a non-resin-coated carrier iron powder (for example, Nippon Tetsuko Co., Ltd. E
FV200/300) 90 g under the above environment in an aluminum pot with a volume of approximately 200 c, c, (hold by hand and shake up and down approximately 50 times)
The toner particles are mixed and the tripocharge amount of the toner particles is measured by a conventional blow-off method using an aluminum cell with a 400 mesh screen.
この方法によって、測られたトリポ電荷が負になるトナ
ー粒子を負帯電性のトナー粒子とする。By this method, toner particles whose measured tripocharge is negative are defined as negatively chargeable toner particles.
また、トナー粒子の体積平均粒子径は5〜30μ■、好
ましくは7〜15μ脂が良い0個数分布における4終腸
以下の含有量は、2%〜20%、好ましくは2〜18%
が良い。In addition, the volume average particle diameter of the toner particles is 5 to 30μ■, preferably 7 to 15μ.The content of 4 endomeres or less in the zero number distribution is 2% to 20%, preferably 2 to 18%.
is good.
トナーの粒径の測定装置としてはコールタ−カウンター
T^−■型(コールタ−社製)を用い、個数平均分布お
よび体積平均分布を出力するインターフェイス(日科機
製)および0X−1パーソナルコンビ、−タ(キャノン
製)を接続し、電解液は1級塩化ナトリウムを用いて1
%NaC!!水溶液を調製する。測定法と1.では前記
電解水溶液100〜・150sffi中に分散剤として
界面活性剤、好ましくはアルキルベンゼンスルホン酸塩
を0.1”5mi!加え、さらに測定試料を0.5〜5
0mg加える。試料を懸濁した電解液は超音波分散機で
約1〜3分間分散処理を行い、前記コールタ−カウンタ
ーTA−11型により、アパチャーとして100 pア
パチャーを用いて2〜・40にの粒子の粒度分布を測定
して体積平均分布2個数平均分布を求める。A Coulter Counter T^-■ model (manufactured by Coulter Co., Ltd.) was used as the toner particle size measuring device, and an interface (manufactured by Nikkaki Machinery Co., Ltd.) that outputs the number average distribution and volume average distribution, and 0X-1 personal combination, - (manufactured by Canon), and the electrolyte is 1st class sodium chloride.
%NaC! ! Prepare an aqueous solution. Measurement method and 1. Then, 0.1"5 mi! of a surfactant, preferably an alkylbenzenesulfonate salt, is added as a dispersant to 100 to 150 sffi of the electrolytic aqueous solution, and 0.5 to 5 sffi of the measurement sample is added.
Add 0mg. The electrolyte in which the sample was suspended was dispersed for about 1 to 3 minutes using an ultrasonic dispersion machine, and then dispersed using the Coulter Counter TA-11 model to obtain a particle size of 2 to 40 using a 100p aperture. The distribution is measured to determine the volume average distribution and the number average distribution.
本発明に係るトナーは、一般的に、次のようにして製造
される。The toner according to the present invention is generally manufactured as follows.
■結着樹脂および場合により磁性体9着色剤としテノ染
顔料などをヘンシェルミキサー等の混合機で均一に分散
させる。(2) Uniformly disperse the binder resin and optionally the magnetic material 9 as a coloring agent such as teno dye pigment using a mixer such as a Henschel mixer.
■上記により得た分散物をニーグー、エクストルーダー
、ロールミル等で溶融混練する。(2) Melt and knead the dispersion obtained above using a Nigu, extruder, roll mill, or the like.
■混練物をカッターミル、ハンマーミル等で粗粉砕した
後、ジェットミル等で微粉砕する。■After coarsely pulverizing the kneaded material with a cutter mill, hammer mill, etc., finely pulverizing it with a jet mill, etc.
−@)微粉砕物をジグザグ分級機等を用いて、粒径分布
をそろえ、分級してトナーどするい
その他トナーの製造法として、重合法、カプセル法等を
用いることが可能である。これらの製造法の概略を以下
に述べる。-@) Using a zigzag classifier or the like, the finely pulverized product is classified to have a uniform particle size distribution, and then the toner is produced.Other toner manufacturing methods include polymerization methods, capsule methods, and the like. An outline of these manufacturing methods will be described below.
(重合法トナー)
■重合性モノマー、必要に応じて重合開始剤9着色剤等
を水性分散媒中で造粒する。(Polymerized toner) (1) A polymerizable monomer and, if necessary, a polymerization initiator 9, a colorant, etc. are granulated in an aqueous dispersion medium.
■造粒されたモノマー組成物粒子を適当な粒子径に分級
する。(2) Classifying the granulated monomer composition particles into appropriate particle sizes.
■上記分級により得た規定内粒径のモノマー組成物粒子
を重合させる。(2) Polymerizing the monomer composition particles having a specified particle size obtained by the above classification.
■適当な処理をして分散剤を取り除いた後、上記により
得た重合生成物をが過9水洗、乾燥してトナーを得る。(2) After removing the dispersant through appropriate treatment, the polymerization product obtained above is washed with water and dried to obtain a toner.
(カプセルトナー)
■樹脂、必要に応じて磁性粉等を混練機等で混練し、溶
融状態のトナー芯材を得る。(Capsule toner) ■Knead resin and, if necessary, magnetic powder etc. using a kneader or the like to obtain a toner core material in a molten state.
■トナー芯材を水中に入れて強く攪拌し、微粒子状の芯
材を作成する。■Pour toner core material into water and stir vigorously to create fine particle core material.
■シェル材溶液中に−L記芯材微粒子を入れ、攪拌しな
がら、貧溶媒を滴下し、芯材表面をシェル材で覆うこと
によりカプセル化する。(2) Put -L core material fine particles into a shell material solution, drop a poor solvent while stirring, and encapsulate the core material surface by covering it with the shell material.
■上記により得たカプセルをか退校、乾燥してトナーを
得る。■ Take the capsules obtained above and dry them to obtain toner.
本発明の画像形成方法に使用される現像剤は、さらに疎
水性シリカ微粉末を含有していることが好ましい。The developer used in the image forming method of the present invention preferably further contains hydrophobic silica fine powder.
負帯電性磁性−成分現像剤の場合、シランカップリング
剤および/またはシリコンオイルで処理された負帯電性
疎水性シリカ微粉末および正帯電性樹脂微粒子を含有し
、かつ負帯電性磁性トナー100重量部に対して前記シ
リカ0.01〜3重量部で含有することが好ましい。In the case of a negatively chargeable magnetic component developer, it contains negatively chargeable hydrophobic silica fine powder and positively chargeable resin fine particles treated with a silane coupling agent and/or silicone oil, and contains 100 weight of negatively chargeable magnetic toner. The content is preferably 0.01 to 3 parts by weight per part of the silica.
本発明に用いるシリカ微粉末としては、ケイ素ハロゲン
化合物の蒸気相酸化により生成された、いわゆる乾式シ
リカまたヒユームドシリカと称されるもので、その表面
がシランカップリング剤および/またはシリコンオイル
で処理されたシリカ微粉末である。The fine silica powder used in the present invention is so-called dry silica or fumed silica, which is produced by vapor phase oxidation of a silicon halide compound, and whose surface has been treated with a silane coupling agent and/or silicone oil. It is a fine silica powder.
好ましいシランカップリング剤としては、ヘキサメチル
ジシラザン(HMDS)が挙げられる。また、好ましい
シリコンオイルとしては、25℃における粘度がおよそ
50−1,000センチストークスのものが用いられ、
例えばジメヂルシリコンオイル、メチルフェニルシリコ
ンオイル、α−メチルスチレン変性シリコンオイル、ク
ロルフェニルシリコンオイル、フッ素変性シリコンオイ
ル等が好ましい。本発明の目的からして、−OH基、−
COOH基。A preferred silane coupling agent includes hexamethyldisilazane (HMDS). Further, as a preferable silicone oil, one having a viscosity of approximately 50 to 1,000 centistokes at 25°C is used,
For example, dimeryl silicone oil, methylphenyl silicone oil, α-methylstyrene-modified silicone oil, chlorphenyl silicone oil, fluorine-modified silicone oil, etc. are preferred. For the purpose of the present invention, -OH group, -
COOH group.
−Nl2基等を多く含有するシリコンオイルは好ましく
ない。Silicone oil containing a large amount of -Nl2 groups, etc. is not preferred.
シリコンオイル処理の方法は公知の技術が用いられ、例
えばシリカ微粉体とシリコンオイルとをヘンシェルミキ
サー等の混合機を用いて直接混合しても良いし、ベース
となるシリカへシリコンオイルを噴射する方法によって
も良い。あるいは適当な溶剤にシリコンオイルを溶解あ
るいは分散せしめた後、ベースのシリカ微粉体とを混合
し、溶剤を除去して作成しても良い。Known techniques are used for the silicone oil treatment; for example, fine silica powder and silicone oil may be directly mixed using a mixer such as a Henschel mixer, or silicone oil may be injected onto the base silica. It's also good. Alternatively, it may be prepared by dissolving or dispersing silicone oil in a suitable solvent, mixing it with the base silica fine powder, and removing the solvent.
本発明におけるシリカ微粉体の疎水化度は、以下の方法
で測定された値を用いる。もちろん、本発明の測定法を
参照しながら他の測定法の適用も可能である。The degree of hydrophobicity of fine silica powder in the present invention uses a value measured by the following method. Of course, other measurement methods can also be applied while referring to the measurement method of the present invention.
密栓式の容器に純水100mfおよび試料1gを入れ、
振とう機にて10分分間上うする。振とう後は例えば数
分間静置し、シリカ粉末層と水層が分離した後、水層を
採取し、500n腸の波長でシリカ微粉体を入れていな
いブランクの純水を基準として透過率を測定し、その透
過率の値をもって処理シリカの疎水化度とするものであ
る。Put 100mf of pure water and 1g of sample into a sealed container,
Mix on a shaker for 10 minutes. After shaking, for example, let stand for several minutes to separate the silica powder layer and the water layer, collect the water layer, and measure the transmittance at a wavelength of 500 nm using blank pure water that does not contain fine silica powder as a reference. The transmittance value is determined as the degree of hydrophobicity of the treated silica.
本発明におけるシリカ微粉体の疎水化度は、80%以上
(より好ましくは83%以上)を有する。The degree of hydrophobicity of the silica fine powder in the present invention is 80% or more (more preferably 83% or more).
疎水化度がこれ以下であると、高湿下でのシリカ微粉体
の水分吸着により高品位の画像が得られなくなる。If the degree of hydrophobicity is less than this, a high-quality image cannot be obtained due to moisture adsorption of the silica fine powder under high humidity.
また、上記シリカ微粉体は負帯電性のものである。Further, the silica fine powder is negatively chargeable.
負帯電性のシリカ微粒子のトリポ値は次の方法で測定さ
れる。すなわち、25℃、50〜60%RHの環境下に
1晩放置されたシリカ微粉体2gと200〜300メツ
シユに主体粒度を持つ、樹脂で被覆されていないキャリ
アー鉄粉(例えば、日本鉄粉社製EFV2GG/30G
) 98g トを前記環境下テオヨソ200c、c、の
容積を持つアルミニウム製ポット中で十分に(手に持っ
て上下におよそ50回振とうする)混合し、400メツ
シユスクリーンを有するアルミニウム製のセルを用いて
通常のブローオフ法により、シリカ微粒子のトリポ電荷
量を測定する。この方法によって、測られたトリポ電荷
が負になるシリカ微粒子を負帯電性のシリカ微粒子と定
義する0本発明においてトリポ電荷量が一100終c/
g〜−300μc/gであるシリカ微粒子が使用される
。The tripo value of negatively charged silica fine particles is measured by the following method. That is, 2 g of fine silica powder left overnight in an environment of 25° C. and 50 to 60% RH and a non-resin-coated carrier iron powder having a main particle size of 200 to 300 mesh (for example, Nippon Iron Powder Co., Ltd.) Manufactured by EFV2GG/30G
) were thoroughly mixed in an aluminum pot with a capacity of 200 c, c, under the above-mentioned environment (by holding it in the hand and shaking it up and down approximately 50 times), and placed in an aluminum cell having a 400 mesh screen. The trypo charge amount of the silica fine particles is measured by the usual blow-off method. By this method, silica particles whose measured trypo charge is negative are defined as negatively charged silica particles.In the present invention, the trypo charge amount is 1100 c/
Silica microparticles having a particle size of ~-300 μc/g are used.
上記シリカ微粒子はトナー粒子100重量部に対して0
.01〜3重量部のときに効果を発揮し、特に好ましく
は、0.05〜2重量部添加した際に優れた安定性を有
する現像剤を提供するものである。The above silica fine particles are 0% per 100 parts by weight of toner particles.
.. The effect is exhibited when the amount is 0.01 to 3 parts by weight, and particularly preferably, a developer having excellent stability is provided when added in an amount of 0.05 to 2 parts by weight.
0.01重量部に満たない場合画像濃度低下の原因とな
り、また、3重量部を越えるとカブリが抑えられず好ま
しくない。If it is less than 0.01 parts by weight, it causes a decrease in image density, and if it exceeds 3 parts by weight, fogging cannot be suppressed, which is not preferable.
添加形態について好ましい態様を述べれば現像剤重量に
対して0.01−1.5重量部の処理されたシリカ微粉
体がトナー粒子表面に付着している状態があるのがよい
。Regarding the preferred form of addition, it is preferable that 0.01 to 1.5 parts by weight of the treated silica fine powder be attached to the surface of the toner particles based on the weight of the developer.
[実施例] 以下、部は重量部を意味する。[Example] Hereinafter, parts mean parts by weight.
実施例1
上記混合物を180°Cに加熱した2軸ルーグーにて溶
融混練した後に冷却し、冷却物をハンマーミル(IJH
IjE式粉JiN&)にて、開口径2層厘のメツシュを
パス程度まで粗粉砕し、次いでジェットミル(風力式粉
砕機)にて、10JL程度まで微粉砕した。微粉砕品を
OS分級器(風力式分級器)にてコールタ−カウンター
にて測定した体積平均粒径が11.5μ■となる様に分
級して、負荷電性の絶縁性磁性トナーを調製した。Example 1 The above mixture was melt-kneaded in a two-screw Rougoo heated to 180°C, cooled, and the cooled mixture was milled in a hammer mill (IJH
A mesh with an opening diameter of two layers was coarsely ground to a pass level using an IjE type powder (JiN&), and then finely ground to about 10 JL using a jet mill (wind-powered grinder). The finely pulverized product was classified using an OS classifier (wind-type classifier) so that the volume average particle diameter measured with a Coulter counter was 11.5μ■, and a negatively charged insulating magnetic toner was prepared. .
この絶縁性磁性トナーは、鉄粉キャリアに対するトリポ
電荷量がブローオフ法による測定で一13終c/gであ
った。This insulating magnetic toner had a tripocharge amount of 113 c/g with respect to the iron powder carrier as measured by the blow-off method.
次に、この負帯電性磁性トナー100部に対し、ステア
リン酸亜鉛(堺化学社製5Z−2000)を0.1部お
よび疎水性シリカ微粉末(BET比表面積130II2
/gの乾式シリカをヘキサメチルジシラザンで処理した
後に、ジメチルシリコーンで処理したもの;疎水化度9
5%、トリポ電荷量−1901Lc/g) 0.4部を
加えて、ヘンシェルミキサーで混合し、−成分現像剤と
した。Next, to 100 parts of this negatively charged magnetic toner, 0.1 part of zinc stearate (manufactured by Sakai Chemical Co., Ltd. 5Z-2000) and fine hydrophobic silica powder (BET specific surface area 130II2) were added.
/g of dry silica treated with hexamethyldisilazane and then treated with dimethyl silicone; degree of hydrophobicity 9
5%, tripo charge amount -1901 Lc/g) was added and mixed in a Henschel mixer to prepare a -component developer.
得られた現像剤を市販の複写機FC−5(キャノン社製
、 apc積層型負帯電感光体、ドラム直径φ30を使
用した曲率分離タイプ、 −1,OkVをバイアス印加
した除電針)を反転現像用に改造しく第1図である転写
条件(Vtr= +700 V)下、感光ドラムと現像
ドラム(磁石内包)上の現像剤層を非接触に間隙を設定
し、交流バイアス(f = 1.800Hz。The obtained developer was subjected to reversal development using a commercially available copying machine FC-5 (manufactured by Canon Co., Ltd., APC laminated type negatively charged photoreceptor, curvature separation type using a drum diameter of φ30, static elimination needle applied with a bias of -1,000 kV). Under the transfer conditions shown in Figure 1 (Vtr = +700 V), a gap was set so that the developer layers on the photosensitive drum and the developing drum (with magnet included) were not in contact with each other, and an alternating current bias (f = 1.800 Hz) was modified for use. .
V pp” 1 、EiOOV )および直流バイアス
(Voe=−500V)とを現像ドラムに印加としなが
ら画出しを行なった0画出しされ、加熱加圧ローラ定着
されたトナ一定着画像を下記の如く評価したい結果を第
1表に示す。Vpp" 1, EiOOV) and DC bias (Voe=-500V) were applied to the developing drum to produce an image. The toner fixed image after 0-image printing and fixed by heating and pressure roller is shown below. Table 1 shows the results that we would like to evaluate.
(1)感光体表面状態:通常の複写機用普通紙(75g
/厘2) 1000枚通紙後、感光体表面の水との接触
角を測定する。(1) Photoconductor surface condition: Normal copying machine plain paper (75g
/厘2) After passing 1000 sheets, measure the contact angle with water on the surface of the photoreceptor.
数値は接触角(θ)の値
(2)画像濃度二通常の複写機用普通紙(75g/m2
)1000枚通紙時の画像濃度謔持によ
り評価した。The numerical value is the contact angle (θ) value (2) Image density 2 Ordinary copying machine plain paper (75 g/m2
) Evaluation was made by maintaining image density when 1000 sheets were passed.
O(良):1.35以上、Δ(可):1.0〜1.34
゜×(不可):1.0未満
(3)転写状態:転写条件として厳しい、120g/m
2の厚紙を通紙し、転写抜は状態に
より評価した。O (good): 1.35 or more, Δ (fair): 1.0 to 1.34
゜× (not possible): Less than 1.0 (3) Transfer condition: Strict transfer conditions, 120 g/m
A thick paper No. 2 was passed through the paper, and transfer removal was evaluated based on the condition.
0:良好、Δ:実用可2×=実用不可
(0@付状態850g/腸2の8紙を1,000枚通紙
し、紙詰りの発生状態を評価した。0: Good, Δ: Practical 2× = Not Practical (1,000 sheets of 8 sheets of 850 g/intestine 2 with 0@ were passed through, and the occurrence of paper jams was evaluated.
0 : I Ii1以内/x、ooo 枚。0: I Ii1 or less/x, ooo pieces.
Δ:2〜4回/1,000枚。Δ: 2 to 4 times/1,000 sheets.
×:5回置−)、/1,009枚
(5)紙 跡:全へ夕画像を出力し、その均一性によ
り評価した。×: 5 rotations -), /1,009 sheets (5) Paper trace: An evening image was output on all pages and evaluated based on its uniformity.
O:濃度差0.05以内、Δ:同0.08〜0.15゜
×:同0.16以上
(6)画像品質:トナーの飛び散り、ガサツキ等を目視
で評価した。O: Density difference within 0.05, Δ: 0.08 to 0.15° ×: 0.16 or more (6) Image quality: Toner scattering, roughness, etc. were visually evaluated.
O:良好、Δ:実用可、×:実用不可
実施例2
転写条件を、V tr/ V prの比が−0,7にな
るように変更する以外は、実施例1と同様にして画出し
をおこなった。結果を第1表に示す。O: Good, Δ: Practical, ×: Not Practical Example 2 Images were printed in the same manner as in Example 1, except that the transfer conditions were changed so that the ratio of V tr / V pr was -0.7. I did it. The results are shown in Table 1.
実施例3
転写条件を、 V tr/ V prの比が−1,5に
なるように変更する以外は、実施例1と同様にして画出
しをおこなった。結果を第1表に示す。Example 3 Image printing was carried out in the same manner as in Example 1, except that the transfer conditions were changed so that the ratio of V tr / V pr was −1.5. The results are shown in Table 1.
実施例4
被膜性物質として、ステアリン酸アルミニウムを使用す
ることを除いて、実施例1と同様にして画出しをおこな
った。結果を第1表に示す。Example 4 Image formation was carried out in the same manner as in Example 1, except that aluminum stearate was used as the coating material. The results are shown in Table 1.
実施例5
被膜性物質として、ラウリル酸マグネシウムを使用する
ことを除いて、実施例1と同様にして現像剤を調製し、
実施例1と同様にして画出しをおこない評価した。結果
を第1表に示す。Example 5 A developer was prepared in the same manner as in Example 1, except that magnesium laurate was used as the film material,
Images were produced and evaluated in the same manner as in Example 1. The results are shown in Table 1.
実施例6
被膜性物質として、ミリスチン酸カルシウムを使用する
ことを除いて、実施例1と同様にして現像剤を調製し、
実施例1と同様にして画出しをおこない評価した。結果
を第1表に示す。Example 6 A developer was prepared in the same manner as in Example 1, except that calcium myristate was used as the film material,
Images were produced and evaluated in the same manner as in Example 1. The results are shown in Table 1.
実施例7
被膜性物質として、ジメチルシリコンオイルを使用する
ことを除いて、実施例1と同様にして現像剤を調製し、
実施例1と同様にして画出しをおこない評価した。結果
を第1表に示す。Example 7 A developer was prepared in the same manner as in Example 1 except that dimethyl silicone oil was used as the film material,
Images were produced and evaluated in the same manner as in Example 1. The results are shown in Table 1.
実施例8
被膜性物質として、メチルフェニルシリコンオイルを使
用することを除いて、実施例1と同様にして現像剤を調
製し、実施例1と同様にして画出しをおこない評価した
。結果を第1表に示す。Example 8 A developer was prepared in the same manner as in Example 1, except that methylphenyl silicone oil was used as the film material, and images were formed and evaluated in the same manner as in Example 1. The results are shown in Table 1.
実施例9
ステアリン酸亜鉛の添加量として、0.02部使用する
ことを除いて、実施例1と同様にして現像剤を調製し、
実施例1と同様にして画出しをおこない評価した。結果
を第1表に示す。Example 9 A developer was prepared in the same manner as in Example 1, except that 0.02 part of zinc stearate was used,
Images were produced and evaluated in the same manner as in Example 1. The results are shown in Table 1.
実施例10
ステアリン酸亜鉛の添加量を0.8部にすることを除い
て、実施例1と同様にして現像剤を調製し、実施例1と
同様にして画出しをおこない評価した。結果を第1表に
示す。Example 10 A developer was prepared in the same manner as in Example 1, except that the amount of zinc stearate added was 0.8 parts, and images were produced and evaluated in the same manner as in Example 1. The results are shown in Table 1.
比較例1
被膜性物質を使用しないことを除いて、実施例1ど同様
にして現像剤を調製し、実施例1と同様にして画出しを
おこない評価した。結果を第1表に示す。Comparative Example 1 A developer was prepared in the same manner as in Example 1, except that no film material was used, and images were produced and evaluated in the same manner as in Example 1. The results are shown in Table 1.
比較例2
転写条件をV tr/ V prの比が−2,0になる
ように変更することを除いて、実施例1と同様にして現
像剤を調製し、実施例1と同様にして画出しをおこない
評価した。結果を第1表に示す。Comparative Example 2 A developer was prepared in the same manner as in Example 1, except that the transfer conditions were changed so that the ratio of V tr / V pr was -2.0, and an image was produced in the same manner as in Example 1. The test was carried out and evaluated. The results are shown in Table 1.
比較例3
転写条件をVtr/Vprの比が−0,3になるように
変更することを除いて、実施例1と同様にして現像剤を
調製し、実施例1と同様にして画出しをおこない評価し
た。結果を第1表に示す。Comparative Example 3 A developer was prepared in the same manner as in Example 1, except that the transfer conditions were changed so that the ratio of Vtr/Vpr was -0.3, and image formation was performed in the same manner as in Example 1. was conducted and evaluated. The results are shown in Table 1.
比較例4
ステアリン酸亜鉛の添加量として、1.5部使用する事
を除いて、実施例1と同様にして現像剤を調製し、実施
例1と同様にして画出しを行ない評価した。結果を第1
表に示す。Comparative Example 4 A developer was prepared in the same manner as in Example 1, except that 1.5 parts of zinc stearate was added, and images were produced and evaluated in the same manner as in Example 1. Results first
Shown in the table.
(以下余白)(Margin below)
添付図面中、第1図は本発明の実施例で使用した画像形
成装置を概略的に示した図であり、第2図は、除電ブラ
シに交流バイアスおよび直流/くイアスを印加している
転写部分を拡大している図を示す・
l・・・感光ドラム 2・・・−成帯電器3・・・
転写帯電器 4・・・現像スリーブ5・・・露光
6・・・イレース露光7・・・加熱加圧ロ
ーラ定着器
8・・・ブレードクリーニング装置In the accompanying drawings, FIG. 1 is a diagram schematically showing an image forming apparatus used in an embodiment of the present invention, and FIG. 2 is a diagram schematically showing an image forming apparatus used in an embodiment of the present invention, and FIG. The diagram shows an enlarged view of the part. l...Photosensitive drum 2...-Charger 3...
Transfer charger 4...Developing sleeve 5...Exposure
6...Erase exposure 7...Heating pressure roller fixing device 8...Blade cleaning device
Claims (1)
、静電荷像保持体上に形成された現像剤画像を転写材へ
静電転写する画像形成方法において、水との接触角が8
0%以上の滑性面を前記保持体表面に形成させる被膜性
物質を0.01〜1.0重量部(対トナー100重量部
)含有する一成分系現像剤を使用し、一次帯電電界V_
p_rと転写帯電電界V_t_rとの比(V_t_r/
V_p_r)が負となる条件下及び(V_t_r/V_
p_r)の絶対値が0.5乃至1.6である条件下で、
トナー画像を静電転写することを特徴とする画像形成方
法。In an image forming method in which an electrostatic image on an electrostatic image carrier is developed with a one-component developer and the developer image formed on the electrostatic image carrier is electrostatically transferred to a transfer material, contact with water 8 corners
A one-component developer containing 0.01 to 1.0 parts by weight (100 parts by weight of toner) of a coating material that forms a smooth surface of 0% or more on the surface of the holder is used, and the primary charging electric field V_
The ratio between p_r and transfer charging electric field V_t_r (V_t_r/
Under conditions where V_p_r) is negative and (V_t_r/V_
Under the condition that the absolute value of p_r) is 0.5 to 1.6,
An image forming method characterized by electrostatically transferring a toner image.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63159349A JP2584281B2 (en) | 1988-06-29 | 1988-06-29 | Image forming method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63159349A JP2584281B2 (en) | 1988-06-29 | 1988-06-29 | Image forming method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0210387A true JPH0210387A (en) | 1990-01-16 |
JP2584281B2 JP2584281B2 (en) | 1997-02-26 |
Family
ID=15691904
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63159349A Expired - Lifetime JP2584281B2 (en) | 1988-06-29 | 1988-06-29 | Image forming method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2584281B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2016156958A (en) * | 2015-02-24 | 2016-09-01 | 株式会社リコー | Image forming apparatus |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5451532A (en) * | 1977-09-30 | 1979-04-23 | Hitachi Metals Ltd | Magnetic toner and production thereof |
JPS5827503A (en) * | 1981-08-03 | 1983-02-18 | パ−マ・エセ・ピ・ア | Mold apparatus for producing shoe sole |
JPS63135980A (en) * | 1986-11-27 | 1988-06-08 | Olympus Optical Co Ltd | Pressure transfer method for conductive toner image |
-
1988
- 1988-06-29 JP JP63159349A patent/JP2584281B2/en not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5451532A (en) * | 1977-09-30 | 1979-04-23 | Hitachi Metals Ltd | Magnetic toner and production thereof |
JPS5827503A (en) * | 1981-08-03 | 1983-02-18 | パ−マ・エセ・ピ・ア | Mold apparatus for producing shoe sole |
JPS63135980A (en) * | 1986-11-27 | 1988-06-08 | Olympus Optical Co Ltd | Pressure transfer method for conductive toner image |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2016156958A (en) * | 2015-02-24 | 2016-09-01 | 株式会社リコー | Image forming apparatus |
Also Published As
Publication number | Publication date |
---|---|
JP2584281B2 (en) | 1997-02-26 |
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