JPH04177367A - Toner for electrostatic charge image development and image formation therewith - Google Patents
Toner for electrostatic charge image development and image formation therewithInfo
- Publication number
- JPH04177367A JPH04177367A JP2307887A JP30788790A JPH04177367A JP H04177367 A JPH04177367 A JP H04177367A JP 2307887 A JP2307887 A JP 2307887A JP 30788790 A JP30788790 A JP 30788790A JP H04177367 A JPH04177367 A JP H04177367A
- Authority
- JP
- Japan
- Prior art keywords
- toner
- image
- frictional
- positive charge
- styrene
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 230000015572 biosynthetic process Effects 0.000 title description 2
- 238000000034 method Methods 0.000 claims abstract description 38
- 239000011347 resin Substances 0.000 claims abstract description 15
- 229920005989 resin Polymers 0.000 claims abstract description 15
- 239000003086 colorant Substances 0.000 claims abstract description 9
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 24
- 239000011230 binding agent Substances 0.000 claims description 10
- 229910017464 nitrogen compound Inorganic materials 0.000 claims description 3
- 150000002830 nitrogen compounds Chemical class 0.000 claims description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 abstract description 6
- -1 nitrogenous compound Chemical class 0.000 abstract description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 4
- 229910052799 carbon Inorganic materials 0.000 abstract description 4
- WURBFLDFSFBTLW-UHFFFAOYSA-N benzil Chemical group C=1C=CC=CC=1C(=O)C(=O)C1=CC=CC=C1 WURBFLDFSFBTLW-UHFFFAOYSA-N 0.000 abstract 1
- 229920001577 copolymer Polymers 0.000 description 18
- 239000000975 dye Substances 0.000 description 11
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 7
- 108091008695 photoreceptors Proteins 0.000 description 7
- 239000000049 pigment Substances 0.000 description 5
- 230000001105 regulatory effect Effects 0.000 description 5
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 229910052804 chromium Inorganic materials 0.000 description 3
- 239000011651 chromium Substances 0.000 description 3
- 230000003247 decreasing effect Effects 0.000 description 3
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000003921 oil Substances 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
- 239000004698 Polyethylene Substances 0.000 description 2
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-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
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000000981 basic dye Substances 0.000 description 2
- 239000008119 colloidal silica Substances 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229940107698 malachite green Drugs 0.000 description 2
- FDZZZRQASAIRJF-UHFFFAOYSA-M malachite green Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1C(C=1C=CC=CC=1)=C1C=CC(=[N+](C)C)C=C1 FDZZZRQASAIRJF-UHFFFAOYSA-M 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 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
- GUYIZQZWDFCUTA-UHFFFAOYSA-N (pentadecachlorophthalocyaninato(2-))-copper Chemical compound [Cu+2].N1=C([N-]2)C3=C(Cl)C(Cl)=C(Cl)C(Cl)=C3C2=NC(C2=C(Cl)C(Cl)=C(Cl)C(Cl)=C22)=NC2=NC(C2=C(Cl)C(Cl)=C(Cl)C(Cl)=C22)=NC2=NC2=C(C(Cl)=C(C(Cl)=C3)Cl)C3=C1[N-]2 GUYIZQZWDFCUTA-UHFFFAOYSA-N 0.000 description 1
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical group C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
- IICCLYANAQEHCI-UHFFFAOYSA-N 4,5,6,7-tetrachloro-3',6'-dihydroxy-2',4',5',7'-tetraiodospiro[2-benzofuran-3,9'-xanthene]-1-one Chemical compound O1C(=O)C(C(=C(Cl)C(Cl)=C2Cl)Cl)=C2C21C1=CC(I)=C(O)C(I)=C1OC1=C(I)C(O)=C(I)C=C21 IICCLYANAQEHCI-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Natural products CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000001692 EU approved anti-caking agent Substances 0.000 description 1
- 239000013032 Hydrocarbon resin Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 208000037062 Polyps Diseases 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-N Salicylic acid Natural products OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 229920007962 Styrene Methyl Methacrylate Polymers 0.000 description 1
- 239000003082 abrasive agent Substances 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 description 1
- 150000001639 boron compounds Chemical class 0.000 description 1
- 229910000420 cerium oxide Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000003822 epoxy resin Substances 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
- 238000004898 kneading Methods 0.000 description 1
- MOUPNEIJQCETIW-UHFFFAOYSA-N lead chromate Chemical compound [Pb+2].[O-][Cr]([O-])(=O)=O MOUPNEIJQCETIW-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 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
- CXKWCBBOMKCUKX-UHFFFAOYSA-M methylene blue Chemical compound [Cl-].C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 CXKWCBBOMKCUKX-UHFFFAOYSA-M 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 229920001490 poly(butyl methacrylate) polymer Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920002102 polyvinyl toluene Polymers 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 229940051201 quinoline yellow Drugs 0.000 description 1
- 235000012752 quinoline yellow Nutrition 0.000 description 1
- 239000004172 quinoline yellow Substances 0.000 description 1
- IZMJMCDDWKSTTK-UHFFFAOYSA-N quinoline yellow Chemical compound C1=CC=CC2=NC(C3C(C4=CC=CC=C4C3=O)=O)=CC=C21 IZMJMCDDWKSTTK-UHFFFAOYSA-N 0.000 description 1
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
- 229940081623 rose bengal Drugs 0.000 description 1
- 229930187593 rose bengal Natural products 0.000 description 1
- STRXNPAVPKGJQR-UHFFFAOYSA-N rose bengal A Natural products O1C(=O)C(C(=CC=C2Cl)Cl)=C2C21C1=CC(I)=C(O)C(I)=C1OC1=C(I)C(O)=C(I)C=C21 STRXNPAVPKGJQR-UHFFFAOYSA-N 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 229920006249 styrenic copolymer Polymers 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- XOSXWYQMOYSSKB-LDKJGXKFSA-L water blue Chemical compound CC1=CC(/C(\C(C=C2)=CC=C2NC(C=C2)=CC=C2S([O-])(=O)=O)=C(\C=C2)/C=C/C\2=N\C(C=C2)=CC=C2S([O-])(=O)=O)=CC(S(O)(=O)=O)=C1N.[Na+].[Na+] XOSXWYQMOYSSKB-LDKJGXKFSA-L 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
Landscapes
- 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、静電記録、静電印刷などにおける
静電荷像を現像するための乾式トナー及びそれを用いる
画像形成方法に関し、更に詳しくは正荷電制御剤として
特定の化合物を含有する静電荷像現像用トナー及びそれ
を用い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 a dry toner for developing electrostatic images in electrophotography, electrostatic recording, electrostatic printing, etc., and an image forming method using the same. More specifically, the present invention relates to an electrostatic image developing toner containing a specific compound as a positive charge control agent and an image forming method using the same.
電子写真感光体や静電記録体なとの上に形成された静電
荷像を現像する手段としては、液体現像剤を用いる方法
(湿式現像法)と、結着樹脂中に着色剤を分散させたト
ナーあるいはこのトナーを固体キャリアと混合した一成
分型ないし二成分型乾式現像剤を用いる方式(乾式現像
法)とが一般に採用されている。そして、これら方式に
はそれぞれ長所・短所があるが、現在では、乾式現像法
が多く利用されている。There are two methods for developing electrostatic images formed on electrophotographic photoreceptors and electrostatic recording materials: a method that uses a liquid developer (wet development method), and a method that uses a colorant dispersed in a binder resin. A method (dry development method) using a toner or a one-component type or two-component type dry developer in which the toner is mixed with a solid carrier is generally adopted. Although each of these methods has its own advantages and disadvantages, the dry developing method is currently widely used.
ところで、前記のトナー(現像粉)においては、単に結
着樹脂に染料、顔料などの着色剤を分散させただけのも
のでは望ましい帯電性が得られないため、これに荷電制
御剤が適当量添加されているのが普通である。従来の荷
電制御剤の代表例としては、(1)トナーに正電荷を与
えるものとして、例えば、ニグロシン系の油溶性染料、
第四級アンモニウム塩、アルキル基を有するアジン系染
料、塩基性染料、塩基性染料のレーキなどが、また、(
ii)トナーに負電荷を与えるものとして、例えば含ク
ロムモノアゾ錯体、含クロムサリチル酸化合物錯体、含
クロム有機染料(銅フタロシアニングリーン、含クロル
モノアゾ染料)のごとき含金属染料が挙げられる。By the way, in the above-mentioned toner (developer powder), desired charging properties cannot be obtained if colorants such as dyes and pigments are simply dispersed in a binder resin, so an appropriate amount of a charge control agent is added to the toner (developer powder). It is normal that this is done. Typical examples of conventional charge control agents include (1) agents that impart a positive charge to toner, such as nigrosine-based oil-soluble dyes;
Quaternary ammonium salts, azine dyes having alkyl groups, basic dyes, lakes of basic dyes, etc.
ii) Examples of things that impart a negative charge to the toner include metal-containing dyes such as chromium-containing monoazo complexes, chromium-containing salicylic acid compound complexes, and chromium-containing organic dyes (copper phthalocyanine green, chlorine-containing monoazo dyes).
だが、こうした従来の荷電制御剤を含有したトナーは、
初期には良好な現像特性を示すものの寿命が短く、従っ
て長時間の使用では感光体へフィルミングを生じさせる
といった不都合な現象が往々にして認められている。こ
れは、従来の荷電制御剤の性質が一定せず、安定性に欠
けるために起因するものである。加えて、こうした従来
の荷電制御剤の多くは、トナー製造での熱混練時に分散
したり、機械的衝動や摩擦、温湿度条件の変化などによ
り分解あるいは変質しやすく、こうしたことが荷電制御
性の低下する現象を一層強めている。However, toners containing these conventional charge control agents,
Although they exhibit good developing characteristics initially, they have a short lifespan, and therefore, when used for a long time, disadvantageous phenomena such as filming on the photoreceptor are often observed. This is due to the fact that the properties of conventional charge control agents are inconsistent and lack stability. In addition, many of these conventional charge control agents are easily dispersed during thermal kneading during toner production, or easily decomposed or deteriorated due to mechanical impulses, friction, changes in temperature and humidity conditions, etc. This is making the phenomenon of decline even stronger.
また、従来の荷電制御剤は環境により変化するものが多
いという傾向もみられる。特に、少なくともトナー搬送
部材、トナー層厚規制部材を有し、トナー搬送部材上に
トナー薄層を形成させ現像を行なう一成分プロセスにお
いては、トナー帯電性の変動がトナー薄層の形成性に大
きく影響し、画像の劣化を引き起こすことがある。いず
れにしてもこれまで提案されてきた荷電制御剤は、長期
にわたって適度の帯電性を持ち得ないものが殆どである
。Furthermore, there is a tendency that many of the conventional charge control agents change depending on the environment. In particular, in a one-component process that includes at least a toner transport member and a toner layer thickness regulating member and develops by forming a thin toner layer on the toner transport member, fluctuations in toner chargeability have a large effect on the ability to form a thin toner layer. may cause image deterioration. In any case, most of the charge control agents that have been proposed so far cannot maintain appropriate chargeability over a long period of time.
本発明は、上記従来技術の有する欠点を克服し、トナー
粒子間又は−成分系現像方式におけるトナーと現像スリ
ーブ若しくはブレードのような帯電付与部材との間で生
じる摩擦帯電が安定で、且つ摩擦帯電量分布がシャープ
で均一であり、使用される現像方法に適した帯電量にコ
ントロールできるトナーを提供することを第1の目的と
し、また摩擦帯電性が過大になりすぎることなく長期に
わたって正に荷電制御された一成分型乾式現像材におけ
るトナーを提供することを第2の目的とする。The present invention overcomes the drawbacks of the above-mentioned prior art, and achieves stable triboelectric charging that occurs between toner particles or between a toner and a charge imparting member such as a developing sleeve or blade in a component-based development system, and Our primary objective is to provide a toner that has a sharp and uniform amount distribution and that can be controlled to the amount of charge appropriate for the developing method used, and that is positively charged over a long period of time without becoming excessively triboelectric. A second object is to provide a toner in a controlled one-component dry developer.
更に、本発明は、常に安定した画像が得られるのは勿論
のこと、耐久性を有するトナーを提供することを第3の
目的とし、また汚染やトナー飛散がなく、連続使用にお
いても初期画像と同等の良質画像が多数枚得られるトナ
ーを提供することを第4の目的とする。Furthermore, the third objective of the present invention is to provide a toner that not only always provides stable images but also has durability, is free from stains and toner scattering, and maintains the same initial image quality even during continuous use. A fourth object is to provide a toner that allows a large number of equally high-quality images to be obtained.
本発明者らは、鋭意研究を重ねた結果、正荷電制御剤と
して特定の窒素化合物を含有するトナーが上記目的に適
合することを知見し、本発明を完成するに至った。As a result of extensive research, the present inventors have found that a toner containing a specific nitrogen compound as a positive charge control agent is suitable for the above purpose, and have completed the present invention.
即ち、本発明によれば、少なくとも結着樹脂と着色剤か
らなるトナーにおいて、正荷電制御剤として下記構造式
(1)で示される硼素化合物を含有することを特徴とす
る静電荷像現像用トナーが提供される。That is, according to the present invention, there is provided a toner for developing electrostatic images, characterized in that the toner comprises at least a binder resin and a colorant, and contains a boron compound represented by the following structural formula (1) as a positive charge control agent. is provided.
(式中、R0〜R4は炭素数1〜18のアルキル基、フ
エニ ル基又はベンジル基を表わす。)
また、薄層化させたトナーを潜像担持体に供給して潜像
を現像する電子写真における一成分現像方式による画像
形成方法において、前記トナーを用いることを特徴とす
る画像形成方法が提供される。(In the formula, R0 to R4 represent an alkyl group having 1 to 18 carbon atoms, a phenyl group, or a benzyl group.) In addition, the toner that has been made into a thin layer is supplied to the latent image carrier to develop the latent image. An image forming method using the one-component development method in photography is provided, which is characterized in that the toner is used.
本発明のトナーにおいて、正荷電制御剤として使用され
る前記構造式で示される正素化合物は、公知の手段で合
成される。該正荷電制御剤は単独で用いてもよいし、2
種を併用してもよい。また、他の正荷電制御剤を併用す
ることもできる。In the toner of the present invention, the positive charge control agent represented by the above structural formula is synthesized by a known method. The positive charge control agent may be used alone, or 2
Seeds may also be used. Moreover, other positive charge control agents can also be used together.
本発明の正荷電制御剤として用いられる前記−般式(1
)で示される化合物の代表例としては、たとえば次のよ
うな化合物が挙げられるが、もちろんこれらに限定され
るものではない。The general formula (1) used as the positive charge control agent of the present invention
) Typical examples of the compounds represented by ) include the following compounds, but are not limited to these, of course.
本発明のトナーは、結着樹脂、着色剤及び前記の正荷電
制御剤を必須成分とする。トナー中の前記正荷電制御剤
の含有量は、結着樹脂の種類、必要に応じて使用される
添加剤の有無、分散方法を含めたトナー製造方法によっ
て決定されるもので、一義的に限定されるものではない
が、通常結着樹脂100重量部に対して0.1〜20重
量部、好ましくは0.2〜lO重量部の範囲である。0
.1重量部未満ではトナーの正帯電性が不足し実用的で
なく、逆に20重量部を越える場合は、トナーの正帯電
性が大きくなりすぎて、流動性低下、転写性低下及び画
像濃度の低下等をもたらすようになり好ましくない。The toner of the present invention includes a binder resin, a colorant, and the positive charge control agent as essential components. The content of the positive charge control agent in the toner is determined by the toner manufacturing method, including the type of binder resin, the presence or absence of additives used as necessary, and the dispersion method, and is uniquely limited. Although not necessarily limited, the amount is usually 0.1 to 20 parts by weight, preferably 0.2 to 10 parts by weight, based on 100 parts by weight of the binder resin. 0
.. If it is less than 1 part by weight, the positive chargeability of the toner will be insufficient, making it impractical; if it exceeds 20 parts by weight, the positive chargeability of the toner will become too large, resulting in decreased fluidity, decreased transferability, and decreased image density. This is undesirable as it causes deterioration of the temperature.
本発明で用いられる着色剤としては、従来からトナー用
着色剤として使用されてきた顔料及び染料の全てが適用
される。具体的には、カーボンブランク、ランプブラン
ク、鉄黒、群青、ニグロシン染料、アニリンブルー、カ
ルフォイルブルー、デュポンオイルレッド、キノリンイ
エロー、メチレンブルークロリド、フタロシアニンブル
ー、フタロシアニングリーン、ハンドイエローG、ロー
ダミン6Cレーキ、クロムイエロー、キナクリドン、入
ンジノンイエロー、マラカイトグリーン、マラカイトグ
リーンへキサレート、オイルブランク、アゾオイルブラ
ンク、ローズベンガル、モノアゾ系染顔料、ジスアゾ系
染顔料、トリスアゾ系染顔料及びこれらの混合物などが
挙げられる。As the colorant used in the present invention, all pigments and dyes conventionally used as colorants for toners can be used. Specifically, carbon blank, lamp blank, iron black, ultramarine blue, nigrosine dye, aniline blue, carfoil blue, DuPont oil red, quinoline yellow, methylene blue chloride, phthalocyanine blue, phthalocyanine green, hand yellow G, rhodamine 6C lake, Examples include chrome yellow, quinacridone, quinacridone yellow, malachite green, malachite green hexalate, oil blank, azo oil blank, rose bengal, monoazo dyes and pigments, disazo dyes and pigments, trisazo dyes and pigments, and mixtures thereof. .
また、本発明で用いられる結着樹脂も、前記着色剤と同
様に、これまでトナー用結着樹脂として使用されてきた
ものの全てが適用される。具体的には、ポリスチレン、
ポリp−クロロスチレン、ポリビニルトルエンなどのス
チレン及びその置換体の単重合体、スチレン−p−クロ
ロスチレン共重合体、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−とニル
ナフタレン共重合体、スチレン−アクリル酸メチル共重
合体、スチレン−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−メタクリル酸メチル共重合
体、スチレン−メタクリル酸エチル共重合体、スチレン
−メタクリル酸ブチル共重合体、スチレン−〇−クロル
メタ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、スチレンーヒニルエチルエーテル共重合体、スチレ
ンーヒ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、スチレン−マ
レイン酸共重合体、スチレン−マレイン酸エステル共重
合体などのスチレン系共重合体゛ポリメチルメタクリレ
ート、ポリブチルメタクリレート、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、ポリエ
ステル、ポリウレタン、ポリアミド、エポキシ樹脂、ポ
リビニルブチラール、ポリアクリル酸樹脂、ロジン、変
性ロジン、テルペン樹脂、フェノール樹脂、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挙げられ、これらは単
独であるいは2種以上混合して使用される。Further, as for the binder resin used in the present invention, all the binder resins that have been used hitherto as binder resins for toners can be used, similarly to the colorant described above. Specifically, polystyrene,
Monopolymers of styrene and its substituted products such as polyp-chlorostyrene and polyvinyltoluene, styrene-p-chlorostyrene copolymers, styrene-propylene copolymers,
Styrene-vinyltoluene copolymer, styrene and nilnaphthalene copolymer, styrene-methyl acrylate copolymer, styrene-ethyl acrylate copolymer, styrene-butyl acrylate copolymer, styrene-octyl acrylate copolymer Polymer, styrene-methyl methacrylate copolymer, styrene-ethyl methacrylate copolymer, styrene-butyl methacrylate copolymer, styrene-〇-methyl chloromethacrylate copolymer, styrene-acrylonitrile copolymer, styrene - Vinyl methyl ether copolymer, styrene-hinyl ethyl ether copolymer, styrene-hinyl methyl ketone copolymer, styrene-butadiene copolymer, styrene-isoprene copolymer, styrene-acrylonitrile-indene copolymer , styrenic copolymers such as styrene-maleic acid copolymer, styrene-maleic acid ester copolymer, polymethyl methacrylate, polybutyl methacrylate, polyvinyl chloride, polyvinyl acetate, polyethylene, polypropylene, polyester, polyurethane, polyamide , epoxy resin, polyvinyl butyral, polyacrylic acid resin, rosin, modified rosin, terpene resin, phenol resin, aliphatic or alicyclic hydrocarbon resin, aromatic petroleum resin, chlorinated paraffin, paraffin wax, etc. These may be used alone or in combination of two or more.
なお、本発明のトナーには、必要に応じて添加剤を混合
することができる。添加剤としては、例えば四弗化エチ
レン樹脂、ステアリン酸亜鉛のごとき滑剤あるいは酸化
セリウム、炭化珪素等の研摩剤、あるいは例えばコロイ
ダルシリカ、酸化アルミニウム等の流動化付与剤、ケー
キング防止剤、あるいは例えばカーボンブランク、酸化
錫等の導電性付与剤、あるいは低分子量ポリエチレンな
どの定着助剤等がある。Note that additives may be mixed with the toner of the present invention as necessary. Examples of additives include lubricants such as tetrafluoroethylene resin and zinc stearate, abrasives such as cerium oxide and silicon carbide, fluidizing agents such as colloidal silica and aluminum oxide, anti-caking agents, and carbon. Examples include a blank, a conductivity imparting agent such as tin oxide, and a fixing aid such as low molecular weight polyethylene.
本発明のトナーは、電子写真における一成分現像方式に
よる画像形成に特に有用であり、次に本発明の画像形成
方法について説明する。The toner of the present invention is particularly useful for image formation using a one-component development method in electrophotography, and the image forming method of the present invention will be described next.
本発明の画像形成方法は、薄層化させたトナーを潜像担
持体に供給して潜像を現像する電子写真における一成分
現像方式による画像形成方法において、前記した正荷電
制御剤を含有したトナーを用いることを特徴とする。な
お、トナーの薄層化は、通常トナー搬送部材、トナー層
厚規制部材及びトナー補給補助部材を備え、且つ該補給
補助部材とトナー搬送部材並びにトナー層厚規制部材と
トナー搬送部材とが夫々当接している装置を用いて行な
われる。The image forming method of the present invention is an image forming method using a one-component development method in electrophotography in which a thin layer of toner is supplied to a latent image carrier to develop a latent image, and the image forming method contains the positive charge control agent described above. It is characterized by using toner. Note that toner thinning is usually achieved by providing a toner conveying member, a toner layer thickness regulating member, and a toner replenishment auxiliary member, and the replenishing auxiliary member and toner transporting member, and the toner layer thickness regulating member and toner transporting member, respectively. It is carried out using equipment that is in contact with the
図面により、本発明の画像形成方法を更に詳しく説明す
る。The image forming method of the present invention will be explained in more detail with reference to the drawings.
図面は本発明方法の実施に有用な非磁性−成分系トナー
を使用した現像装置の一例の模式的断面図である。図面
において、トナータンク7に内蔵されている本発明のト
ナー6は、トナー補給補助部材5によりトナー供給部材
4に強制的に寄せられ、トナーはトナー供給部材4に供
給される。そして、スポンジローラ4に取り込まれたト
ナーは、トナー供給部材4が矢印方向に回転することに
より、トナー搬送部材2に運ばれ、摩擦され、静電的あ
るいは物理的に吸着し、トナー搬送部材2が矢印方向に
強く回転し、スチール族のトナー厚規制部材3により均
一なトナー薄層が形成されると共に摩擦帯電する。その
後、トナー搬送部材2と接触若しくは近接している静電
潜像担持体1の表面に運ばれ、潜像が現像される。静電
潜像は有機感光体に800■のマイナスDC帯電をした
後、露光し、潜像を形成し現像されるのである。The drawing is a schematic cross-sectional view of an example of a developing device using a non-magnetic-component toner useful in carrying out the method of the present invention. In the drawing, the toner 6 of the present invention contained in a toner tank 7 is forcibly brought to the toner supply member 4 by the toner replenishment auxiliary member 5, and the toner is supplied to the toner supply member 4. When the toner supply member 4 rotates in the direction of the arrow, the toner taken into the sponge roller 4 is transported to the toner conveying member 2, where it is rubbed, electrostatically or physically adsorbed, and is then transferred to the toner conveying member 2. rotates strongly in the direction of the arrow, and a uniform thin layer of toner is formed by the steel-based toner thickness regulating member 3, and is charged by friction. Thereafter, the toner is transported to the surface of the electrostatic latent image carrier 1 that is in contact with or in close proximity to the toner transport member 2, and the latent image is developed. The electrostatic latent image is created by charging the organic photoreceptor with a negative DC charge of 800 cm and then exposing it to light to form a latent image, which is then developed.
このような電子写真における一成分現像方法による画像
形成方法は、トナーの帯電性の変動がトナーの薄層の形
成性に大きく影響を与えるが、本発明のトナーは、正極
性の安定した摩擦帯電性を示し且つ環境安定性にも優れ
ているので、実施の際に適切な帯電量にコントロールす
ることができ、本発明の方法により、長期にわたり、高
品質の画像が得られる。In such an image forming method using a one-component development method in electrophotography, fluctuations in toner chargeability greatly affect the ability to form a thin layer of toner, but the toner of the present invention has stable positive triboelectrification. Since the method of the present invention exhibits high properties and excellent environmental stability, it is possible to control the amount of charge to an appropriate level during implementation, and high-quality images can be obtained over a long period of time by the method of the present invention.
以下、実施例により本発明を更に詳細に説明する。なお
、部は重量部を表わす。Hereinafter, the present invention will be explained in more detail with reference to Examples. Note that parts represent parts by weight.
実施例1
カーボンブランク 1部部上記
組成の混合物をヘンシェルミキサー中で充分撹拌混合し
た後、ロールミルで130〜140℃の温度で約30分
間加熱溶融し、これを室温まで冷却した。得られた混練
物を粉砕分級し、5〜10μsの粒径のトナーを得た。Example 1 1 part of carbon blank A mixture having the above composition was sufficiently stirred and mixed in a Henschel mixer, then heated and melted in a roll mill at a temperature of 130 to 140°C for about 30 minutes, and then cooled to room temperature. The obtained kneaded product was pulverized and classified to obtain a toner having a particle size of 5 to 10 μs.
このトナー100部に対しコロイダルシリカ0.3部を
添加、混合して本発明のトナーを得た。To 100 parts of this toner, 0.3 parts of colloidal silica was added and mixed to obtain the toner of the present invention.
得られたトナーを用いて、図面に示すような現像装置に
て画像出しを行なったところ、良好な画像が得られ、そ
の画像は10万枚プリント後も変らなかった。When the obtained toner was used to form an image using a developing device as shown in the drawing, a good image was obtained, and the image did not change even after printing 100,000 sheets.
また、トナーの帯電量をブローオフ法で測定したところ
、初期の帯電量は+12.7μC/gであり、10万枚
プリント後におけるトナーの帯電量は+11.11μC
/gと初期値と殆ど変らなかった。In addition, when the amount of charge on the toner was measured using the blow-off method, the amount of charge at the initial stage was +12.7 μC/g, and the amount of charge on the toner after printing 100,000 sheets was +11.11 μC.
/g, which was almost unchanged from the initial value.
更に、35℃、90%RHという高湿環境下及び10℃
、15%RHという低湿環境下でも、常温環境のもとて
の複写と同等の画像が得られ、感光体へのトナーフィル
ミングも認められなかった。Furthermore, under a high humidity environment of 35℃ and 90% RH, and at 10℃
Even in a low humidity environment of 15% RH, an image equivalent to the original copy at room temperature was obtained, and no toner filming on the photoreceptor was observed.
実施例2
実施例1における正荷電制御剤の代わりに、構造式(1
)において、R□=C)13、R3=CH3、R4=C
H3、R2”Cl8837で示される化合物を用いた以
外は、実施例1と同様にして本発明のトナーを得た。Example 2 Instead of the positive charge control agent in Example 1, structural formula (1
), R□=C)13, R3=CH3, R4=C
A toner of the present invention was obtained in the same manner as in Example 1 except that the compound represented by H3, R2''Cl8837 was used.
得られたトナーを用いて、実施例1と同様にして画像出
しを行なったところ、良好な画像が得られ、その画像は
10万枚ランニング後も変らなかった。When an image was produced using the obtained toner in the same manner as in Example 1, a good image was obtained, and the image did not change even after running 100,000 copies.
また、トナーの帯電量をブローオフ法で測定したところ
、初期の帯電量は+12.1μC/gであり、10万枚
ランニング後におけるトナーの帯電量は+11.7μC
/gと初期値と殆ど変らなかった。Furthermore, when the amount of charge on the toner was measured using the blow-off method, the amount of charge at the initial stage was +12.1 μC/g, and the amount of charge on the toner after running 100,000 sheets was +11.7 μC.
/g, which was almost unchanged from the initial value.
更に35℃、90%RHという高湿環境下及び10℃、
]5%RHという低湿環境下でも、常湿環境のものでの
複写と同等の画像が得られ、感光体へのトナーフィルミ
ングも認められなかった。Furthermore, under a high humidity environment of 35°C and 90% RH, and at 10°C,
] Even in a low humidity environment of 5% RH, an image equivalent to that obtained in a normal humidity environment was obtained, and no toner filming on the photoreceptor was observed.
実施例3
実施例1における正荷電制御剤の代わりに、構造式(I
)において、R,=CH3、R2=Cl8H37、R3
=CH3、R4”Cl8837で示される化合物を用い
て以外は、実施例1と同様にして本発明のトナーを得た
。Example 3 Instead of the positive charge control agent in Example 1, structural formula (I
), R,=CH3, R2=Cl8H37, R3
A toner of the present invention was obtained in the same manner as in Example 1 except that the compound represented by =CH3, R4''Cl8837 was used.
得られたトナーを用いて、実施例Iと同様にして画像テ
ストを行なったところ、良好な画像が得られた。Using the obtained toner, an image test was conducted in the same manner as in Example I, and a good image was obtained.
得られたトナーを用いて、図面に示すような現像装置に
て画像出しを行なったところ、良好な画像が得られ、そ
の画像は10万枚ランニングプリ。When the obtained toner was used to produce an image using a developing device as shown in the drawing, a good image was obtained, and the image was printed on 100,000 copies.
ト後も変らなかった。It didn't change after that.
また、トナーの帯電量をブローオフ法で測定したところ
、初期の帯電量は+11.3μC/gであり、IO万枚
ラうニング後におけるトナーの帯電量は+109μC/
gと初期値と殆ど変らなかった。Furthermore, when the toner charge amount was measured using the blow-off method, the initial charge amount was +11.3 μC/g, and the toner charge amount after running 10,000 sheets was +109 μC/g.
g was almost unchanged from the initial value.
更に、35℃、90%R+(という高湿環境下及び10
°C115%RHという低湿環境下でも、常温環境のも
とての複写と同等の画像が得られ、感光体−のトナーフ
ィルミングも認められなかった。Furthermore, under a high humidity environment of 35°C, 90% R+, and 10%
Even in a low humidity environment of 115% RH at °C, an image equivalent to the original copy at room temperature was obtained, and no toner filming on the photoreceptor was observed.
請求項(1)の静電荷像現像用トナーは、正荷電制御剤
として前記構造式(1)で示される窒素化合物を含有す
ることから、トナーと現像スリーブ若しくはブレード等
の帯電付与部材との摩擦帯電を正極性の安定した摩擦帯
電性に保持することができる。The toner for developing an electrostatic image according to claim (1) contains the nitrogen compound represented by the structural formula (1) as a positive charge control agent, so that friction between the toner and a charge imparting member such as a developing sleeve or a blade is reduced. Charging can be maintained at a positive and stable triboelectric charging property.
また、該トナーは、機械的衝撃や摩擦更には温湿度条件
等の環境が変化しても、その摩擦帯電性等の諸性能に変
化がない。Further, the toner does not change its various performances such as triboelectric charging properties even if the environment such as mechanical shock, friction, temperature and humidity conditions changes.
このため、請求項(2)の画像形成方法により、地汚れ
やトナーの飛散がなく、連続複写後も初期画像と同等の
高品質画像を得ることができる。Therefore, with the image forming method of claim (2), it is possible to obtain a high-quality image equivalent to the initial image even after continuous copying without background smudge or toner scattering.
また、該方法においては、種々の環境下においても、安
定した高品質画像が得られ、且つ長時間使用しても感光
体にフィルミングすることがない。Moreover, in this method, stable high-quality images can be obtained even under various environments, and there is no filming on the photoreceptor even after long-term use.
図面は本発明の方法の実施に有用な本発明の非磁性−成
分系トナーを用いた現像装置の一例を示す模式断面図で
ある。
1・・静電潜像担持体、2・トナー搬送部材、3・トナ
ー層厚規制部材、4・・トナー供給部材、5・トナー補
助補給部材、6・トナー、7・トナータンク。The drawing is a schematic sectional view showing an example of a developing device using the non-magnetic component toner of the present invention useful for carrying out the method of the present invention. 1. Electrostatic latent image carrier, 2. Toner transport member, 3. Toner layer thickness regulating member, 4. Toner supply member, 5. Toner auxiliary replenishment member, 6. Toner, 7. Toner tank.
Claims (2)
いて、正荷電制御剤として下記構造式( I )で示され
る窒素化合物を含有することを特徴とする静電荷像現像
用トナー。 ▲数式、化学式、表等があります▼ (式中、R_1〜R_4は炭素数1〜18のアルキル基
、フェニル基又はベンジル基を表わす。)(1) A toner for developing an electrostatic image, comprising at least a binder resin and a colorant, and containing a nitrogen compound represented by the following structural formula (I) as a positive charge control agent. ▲There are mathematical formulas, chemical formulas, tables, etc.▼ (In the formula, R_1 to R_4 represent an alkyl group having 1 to 18 carbon atoms, a phenyl group, or a benzyl group.)
を現像する電子写真における一成分現像方式による画像
形成方法において、請求項(1)記載のトナーを用いる
ことを特徴とする画像形成方法。(2) An image forming method using a one-component development method in electrophotography, in which a thin layer of toner is supplied to a latent image carrier to develop a latent image, characterized by using the toner according to claim (1). image forming method.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2307887A JPH04177367A (en) | 1990-11-13 | 1990-11-13 | Toner for electrostatic charge image development and image formation therewith |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2307887A JPH04177367A (en) | 1990-11-13 | 1990-11-13 | Toner for electrostatic charge image development and image formation therewith |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04177367A true JPH04177367A (en) | 1992-06-24 |
Family
ID=17974363
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2307887A Pending JPH04177367A (en) | 1990-11-13 | 1990-11-13 | Toner for electrostatic charge image development and image formation therewith |
Country Status (1)
Country | Link |
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JP (1) | JPH04177367A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111440073A (en) * | 2020-04-24 | 2020-07-24 | 湖北航天化学技术研究所 | Synthetic method and application of combustion speed regulator |
-
1990
- 1990-11-13 JP JP2307887A patent/JPH04177367A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111440073A (en) * | 2020-04-24 | 2020-07-24 | 湖北航天化学技术研究所 | Synthetic method and application of combustion speed regulator |
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