JPH0424646A - Electrostatic latent image developing toner - Google Patents
Electrostatic latent image developing tonerInfo
- Publication number
- JPH0424646A JPH0424646A JP2129597A JP12959790A JPH0424646A JP H0424646 A JPH0424646 A JP H0424646A JP 2129597 A JP2129597 A JP 2129597A JP 12959790 A JP12959790 A JP 12959790A JP H0424646 A JPH0424646 A JP H0424646A
- Authority
- JP
- Japan
- Prior art keywords
- toner
- resin
- antimony
- developer
- amount
- 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
- 229920005989 resin Polymers 0.000 claims abstract description 18
- 239000011347 resin Substances 0.000 claims abstract description 18
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 claims abstract description 15
- 229910001887 tin oxide Inorganic materials 0.000 claims abstract description 12
- 239000000049 pigment Substances 0.000 claims description 3
- 229910052787 antimony Inorganic materials 0.000 claims 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims 1
- 239000003086 colorant Substances 0.000 abstract 2
- 238000006748 scratching Methods 0.000 abstract 1
- 230000002393 scratching effect Effects 0.000 abstract 1
- 230000006641 stabilisation Effects 0.000 abstract 1
- 238000011105 stabilization Methods 0.000 abstract 1
- 229920001577 copolymer Polymers 0.000 description 10
- -1 polypropylene Polymers 0.000 description 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 238000011161 development Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 239000004743 Polypropylene Substances 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 229920001225 polyester resin Polymers 0.000 description 4
- 239000004645 polyester resin Substances 0.000 description 4
- 229920001155 polypropylene Polymers 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 238000007796 conventional method Methods 0.000 description 3
- 239000003822 epoxy resin Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229920000647 polyepoxide Polymers 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 229910000859 α-Fe Inorganic materials 0.000 description 3
- 229910002012 Aerosil® Inorganic materials 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 108091008695 photoreceptors Proteins 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 2
- DZNJMLVCIZGWSC-UHFFFAOYSA-N 3',6'-bis(diethylamino)spiro[2-benzofuran-3,9'-xanthene]-1-one Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC=C(N(CC)CC)C=C1OC1=CC(N(CC)CC)=CC=C21 DZNJMLVCIZGWSC-UHFFFAOYSA-N 0.000 description 1
- JCYPECIVGRXBMO-UHFFFAOYSA-N 4-(dimethylamino)azobenzene Chemical group C1=CC(N(C)C)=CC=C1N=NC1=CC=CC=C1 JCYPECIVGRXBMO-UHFFFAOYSA-N 0.000 description 1
- ACYXOHNDKRVKLH-UHFFFAOYSA-N 5-phenylpenta-2,4-dienenitrile prop-2-enoic acid Chemical compound OC(=O)C=C.N#CC=CC=CC1=CC=CC=C1 ACYXOHNDKRVKLH-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
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 239000013032 Hydrocarbon resin Substances 0.000 description 1
- 229920001890 Novodur Polymers 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
- 239000004793 Polystyrene Substances 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 240000004668 Valerianella locusta Species 0.000 description 1
- 235000003560 Valerianella locusta Nutrition 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 235000012745 brilliant blue FCF Nutrition 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 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
- 239000008119 colloidal silica Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 229920006244 ethylene-ethyl acrylate Polymers 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229920006270 hydrocarbon resin Polymers 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000002689 maleic acids Chemical class 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229920003146 methacrylic ester copolymer Polymers 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 239000001022 rhodamine dye Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 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、静電記録等に使用される静電潜像
現像用トナーに関する。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a toner for developing electrostatic latent images used in electrophotography, electrostatic recording, and the like.
(従来の技術)
電子写真、静電記録等の分野に於ける現像法としては従
来から電荷制御剤等を含有させた5〜20μmに微粉砕
されたトナーとフェライト粉や鉄粉等のキャリアを混合
して作られる所謂2成分現像剤を用いる乾式現像法が一
般に知られている。(Prior art) Development methods in the fields of electrophotography, electrostatic recording, etc. have conventionally used toner containing a charge control agent, finely pulverized to 5 to 20 μm, and a carrier such as ferrite powder or iron powder. A dry development method using a so-called two-component developer prepared by mixing is generally known.
(発明が解決しようとする課題)
しかし、2成分方式に於ては現像枚数の増加と環境条件
によってトナー及びキャリアの摩擦帯電量が異なってく
る。すなわち現像枚数が多くなればなるほどトナー及び
キャリアの摩擦帯電量が大きくなっていき、また低温低
湿の環境下の方が高温高湿の環境下の方よりも摩擦帯電
量が太き(なる。従って低温低湿環境下で現像枚数を多
くしていくと、摩擦帯電量が更に太き(なっていき、画
像濃度の著しい低下、かぶりの増加やキャリアが静電像
支持体に付着するキャリア飛びが発生し、感光体表面及
び定着ローラーを傷つけるといった好ましくない事態を
ひきおこす事があった。(Problem to be Solved by the Invention) However, in the two-component method, the amount of triboelectric charge of the toner and carrier varies depending on the increase in the number of sheets to be developed and the environmental conditions. In other words, as the number of sheets to be developed increases, the amount of triboelectricity of the toner and carrier increases, and the amount of triboelectricity is larger in a low temperature and low humidity environment than in a high temperature and high humidity environment. As the number of sheets developed in a low-temperature, low-humidity environment increases, the amount of triboelectric charge increases, resulting in a significant decrease in image density, increased fogging, and carrier fly-off where carrier adheres to the electrostatic image support. However, undesirable situations such as damage to the surface of the photoreceptor and the fixing roller may occur.
本発明は、上述した2成分現像方式に於ける問題点であ
る摩擦帯電の不安定性を改善し、各環境変化に対しても
安定した画像を得るための荷電制御剤を提供する事を目
的としている。The purpose of the present invention is to provide a charge control agent that improves the instability of triboelectric charging, which is a problem in the above-mentioned two-component development system, and that enables stable images to be obtained even under various environmental changes. There is.
(課題を解決するための手段)
この目的を達成するために、アンチモンをドーピングし
た酸化スズ(Sn02)を添加した。(Means for Solving the Problem) To achieve this objective, antimony-doped tin oxide (Sn02) was added.
(作 用)
この構成により、2成分現像方式に於ける摩擦帯電性を
安定化させることができる。(Function) With this configuration, triboelectric charging properties in a two-component development system can be stabilized.
(実 施 例)
以下、本発明を実施例により更に具体的に説明する。尚
、本発明は、これらの実施例に限定されるものではない
。以下、配合の部数についての内容はすべて重量部数で
ある。(Examples) Hereinafter, the present invention will be explained in more detail with reference to Examples. Note that the present invention is not limited to these examples. Hereinafter, all parts of the formulation are by weight.
・実施例 1゜
・スチレン−アクリル酸エステル系樹脂100B(商品
名 ハイマーTBL−5fl)e 、三洋化成社製)・
低分子量ポリプロピレン 4部
(商品名 ヒ゛ス]−ル55θ−P、三洋化成社製)・
帯電制御剤 2部
(商品名 本゛シトロン E−84、iリエント化学
工業社製 )・アンチモンドーピング型酸化スズ 1部
(商品名 タイベ−り5N−1081石原産業社製)・
ローダミ
ン系染料
(C,1,5olvent
ed
49)4部
(商品名 Aizen SOT Pink−1、作土ケ
谷化学工業社製)
上記材料をヘンシェルミキサーで均一に分散し、分散物
を2軸押用機等で溶融混練し、冷却後、ジェットミル等
で微粉砕し、分級機にて平均粒径11μmの分級品を得
た。この分級品に、0.3重量%の疎水性シリカ(商品
名 R972、日本アエロジル社製)をヘンシェルミキ
サーにて外添し、本発明のマゼンタトナーを得た。この
トナーをフェライトキャリア(商品名 FL−150、
パウダーチック社製)と混合し現像剤とした。この現像
剤の摩擦帯電量をブローオフ法により測定したところ、
−20,OμC/gであった。この現像剤を用いてレー
ザープリンター(商品名 KX−P4450.松下電器
産業社製)で各種環境で連続20にの印字を行ない、摩
擦帯電量及び印字濃度を測定した。環境は次の3つを選
んだ。低温低湿(温度10℃、湿度20%RH)、常温
常湿(温度20℃、湿度60%RH)、高温高湿(温度
32.5℃、湿度80%RH)である。従来との比較の
ためにアンチモンをドーピングした酸化スズを用いなか
った以外は、すべて上記と同じ条件でトナーの製造、現
像剤の製造、試験を行なった。従来と本実施例の試験結
果を第1図及び第2図にまとめた。第1図は現像枚数と
摩擦帯電量の関係を示した図で、第2図は現像枚数と印
字濃度の関係を示す図である。第1図において横軸は現
像枚数、縦軸は摩擦帯電量を示している。第1図におい
て1.2.3は未実施例のトナーを用いた時の特性を示
す線で、線1は高温高湿の時のもので、線2は常温常湿
のもので、絆3は低温低湿のものである。又4,5.6
は従来のトナーを用いた時の特性を示す線で、線4は高
温高湿の時のもので、線5は常温常湿のもので、線6は
低温低湿のものである。第1図から分かるように、本実
施例のものは現像枚数が多くなっても摩擦帯電量はほと
んど変わらず、はぼ一定の摩擦帯電量を有している事が
わかる。しかし従来のほうは現像枚数が多くなるに従っ
て、次第に摩擦帯電量が大きくなっていくことがわかる
。また現像枚数が多くなればなるほど各環境のばらつき
が大きくなっている。第2図において7,8.9は本実
施例のトナーを用いた時の特性を示す線で、線7は高温
高湿の時のもので、線8は常温常湿のもので、線9は低
温低湿のものである。又10,11.12は従来のトナ
ーを用いた時の特性を示す線で、線10は高温高湿の時
のもので、線11は常温常湿のもので、線12は低温低
湿のものである。第2図から分かるように、本実施例の
ものは現像枚数が多くなっても印字濃度はほぼ一定であ
る。しかし、従来のものは現像枚数が多くなればなるほ
どどの環境においても印字濃度が薄くなってい(事がわ
かる。また各環境において現像枚数が多(なればなるほ
どばらつきが大きくなっていく事がわかる。尚、ランニ
ング時の摩擦帯電量測定はブローオフ法により、濃度測
定はマクヘス反射濃度計を用いて測定を行なった。・Example 1゜・Styrene-acrylic acid ester resin 100B (product name Hymer TBL-5fl)e, manufactured by Sanyo Chemical Co., Ltd.)・
4 parts of low molecular weight polypropylene (trade name: Heathyl 55θ-P, manufactured by Sanyo Chemical Co., Ltd.)
2 parts of charge control agent (product name: Citron E-84, manufactured by I-Rient Chemical Industry Co., Ltd.), 1 part of antimony-doped tin oxide (product name: Tyberi 5N-1081, manufactured by Ishihara Sangyo Co., Ltd.).
Rhodamine dye (C, 1,5olvent ed 49) 4 parts (trade name Aizen SOT Pink-1, manufactured by Sakudogaya Chemical Industry Co., Ltd.) The above materials were uniformly dispersed with a Henschel mixer, and the dispersion was mixed with a twin-screw presser, etc. After cooling, the mixture was pulverized using a jet mill or the like, and a classified product having an average particle size of 11 μm was obtained using a classifier. To this classified product, 0.3% by weight of hydrophobic silica (trade name R972, manufactured by Nippon Aerosil Co., Ltd.) was externally added using a Henschel mixer to obtain a magenta toner of the present invention. Transfer this toner to a ferrite carrier (product name FL-150,
(manufactured by Powder Chick Co., Ltd.) to prepare a developer. When the amount of triboelectric charge of this developer was measured by the blow-off method, it was found that:
-20, OμC/g. Using this developer, 20 consecutive prints were performed in various environments using a laser printer (trade name: KX-P4450, manufactured by Matsushita Electric Industrial Co., Ltd.), and the amount of triboelectric charge and print density were measured. The following three environments were selected. They are low temperature and low humidity (temperature 10°C, humidity 20% RH), normal temperature and normal humidity (temperature 20°C, humidity 60% RH), and high temperature and high humidity (temperature 32.5°C, humidity 80% RH). For comparison with the conventional method, toner production, developer production, and testing were conducted under the same conditions as above, except that antimony-doped tin oxide was not used. The test results of the conventional method and this example are summarized in FIGS. 1 and 2. FIG. 1 is a diagram showing the relationship between the number of developed sheets and the amount of triboelectric charge, and FIG. 2 is a diagram showing the relationship between the number of developed sheets and print density. In FIG. 1, the horizontal axis shows the number of developed sheets, and the vertical axis shows the amount of triboelectric charge. In FIG. 1, lines 1.2.3 indicate the characteristics when unexamined toners are used, line 1 is for high temperature and high humidity, line 2 is for normal temperature and humidity, and bond 3 is low temperature and low humidity. Also 4,5.6
are lines showing characteristics when conventional toners are used; line 4 is for high temperature and high humidity, line 5 is for normal temperature and normal humidity, and line 6 is for low temperature and low humidity. As can be seen from FIG. 1, in this example, the amount of triboelectric charge hardly changes even when the number of sheets to be developed increases, and it can be seen that the amount of triboelectricity is almost constant. However, in the conventional case, it can be seen that as the number of developed sheets increases, the amount of triboelectric charge gradually increases. Further, as the number of developed sheets increases, the variation in each environment becomes larger. In FIG. 2, lines 7, 8, and 9 indicate the characteristics when the toner of this example is used. Line 7 is for high temperature and high humidity, line 8 is for normal temperature and humidity, and line 9 is for when the toner is used. is low temperature and low humidity. Lines 10, 11, and 12 indicate the characteristics when conventional toners are used. Line 10 is for high temperature and high humidity, line 11 is for normal temperature and humidity, and line 12 is for low temperature and low humidity. It is. As can be seen from FIG. 2, in this example, the print density remains almost constant even if the number of sheets to be developed increases. However, with the conventional method, the print density becomes thinner in all environments as the number of developed sheets increases.It can also be seen that the dispersion increases as the number of developed sheets increases in each environment. The amount of triboelectric charge during running was measured by the blow-off method, and the density was measured using a Maches reflection densitometer.
・実施例 2゜
・飽和ポリエステル樹脂100部
(商品名
製)
ポリエスタ
、日本合成化学工業社
・低分子量ポリプロピレン 4部
(商品名 ヒ゛スコール660−P 、三洋化成社製)
・帯電制御剤 4部
(商品名 ホ゛ントロン E−84 jリエント化
学工業社製)−7タロシアニン系顔料(C.1.Pig
ment Blue Is3)4部
(商品名 KET BLUE 1(l16 、大日本イ
ンキ化字工業社製)
上記材料を実施例 1.と同じ方法で処理し平均粒径1
1μmの分級品を得た。この分級品に0、3重量%の疎
水性シリカ(商品名 R972、日本アエロジル社製)
と、1.0重量%のアンチモンドーピング型酸化スズ(
商品名 タイベークSN−100,石屋産業社製)とを
ヘンシェルミキサーにて外添し、本発明のシアントナー
を得た。実施例 1.と同じキャリアで現像剤を作成し
、摩擦帯電量を測定したところ、−23、0μC /
gであった。このトナーを実施例1、と同様の条件で2
0 Kの印字を行なったが、同様に各種環境に於て、
本発明トナーの摩擦帯電量は各種環境間でばらつきが少
な(かつランニング時に於ける摩擦帯電量の推移も安定
した結果が得られ、良好な印字濃度を示した。比較のた
めにアンチモンドーピング型酸化スズを用いなかった以
外は全て上記と同じ条件でトナーの製造、現像剤の製造
、試験を行なったところ、得られた画像はランニング枚
数の増加につれて著しく変化しかつ、各環境間のばらつ
きが大きく、実用に耐える現像剤ではなかった。・Example 2゜・100 parts of saturated polyester resin (trade name) Polyester, manufactured by Nippon Gosei Kagaku Kogyo Co., Ltd.・4 parts of low molecular weight polypropylene (trade name: Viscole 660-P, manufactured by Sanyo Chemical Co., Ltd.)
・Charge control agent 4 parts (trade name: Phontron E-84 manufactured by Rient Kagaku Kogyo Co., Ltd.) -7 Talocyanine pigment (C.1.Pig
ment Blue Is3) 4 parts (trade name: KET BLUE 1 (l16, manufactured by Dainippon Ink Kaji Kogyo Co., Ltd.) The above material was treated in the same manner as in Example 1 to obtain an average particle size of 1.
A 1 μm classified product was obtained. This classified product contains 0.3% by weight of hydrophobic silica (trade name R972, manufactured by Nippon Aerosil Co., Ltd.)
and 1.0% by weight of antimony-doped tin oxide (
A cyan toner of the present invention was obtained by externally adding the product (trade name: Tybake SN-100, manufactured by Ishiya Sangyo Co., Ltd.) using a Henschel mixer. Example 1. When a developer was made with the same carrier and the amount of triboelectric charge was measured, it was -23.0μC/
It was g. This toner was used under the same conditions as in Example 1.
0K was printed, but under various environments,
The amount of triboelectric charge of the toner of the present invention showed little variation among various environments (and the transition of the amount of triboelectricity during running was also stable, showing good print density.For comparison, antimony-doped oxidation When producing toner, producing developer, and conducting tests under the same conditions as above except that tin was not used, the resulting images changed significantly as the number of running sheets increased, and there were large variations between each environment. However, the developer was not suitable for practical use.
・実施例 3。・Example 3.
・飽和ポリエステル樹脂 100部
(商品名 ポリエスタ−HI”32θ,日本合成化学工
業社製)
・低分子量ポリプロピレン 3部
(商品名
ヒ′スコ
ル
5e
、三洋化成社製)
・帯電制御剤 4部
(商品名 TP−302 、採土ケ谷化学工業社製)・
C.1.Solvent Yellow 2
13部
(商品名 へ゛リファストイエロー ヰ3120
、オリ エン ト化字工業社製)
上記材料を、実施例 1.と同し方法で処理し、平均粒
径11μmの分級品を得た。この分級品にQ.Q重量%
のアンチモンドーピング型酸化スズ(商品名タイベーク
SN−1 00,石屋産業社製)をヘンシェルミキサ
ーにて外添し、本発明のイエロートナーを得た。このト
ナーを実施例1、と同じキャリアを用いて現像剤を作成
し摩擦帯電量を測定したところ、+21.0μC′gで
あった。このトナーは、正帯電性のトナーであるがこの
トナーを実施例 1.で使用したしーザブリンターを改
造して同様の条件で20にの印字を行なったが、同様に
各種環境に於て、本発明トナーの摩擦帯電量は各種環境
間でばらつきが少なくかつランニング時に於ける摩擦帯
電量の推移も安定した結果が得られ、良好な印字濃度を
示した。比較するためにアンチモンドーピング型酸化ス
ズを用いなかった以外は、すべて上記と同じ条件でトナ
ーの製造、現像剤の製造、試験を行なったところ、得ら
れた画像はランニング枚数の増加につれて著しく変化し
かつ、各環境間のばらつきが大きく、実用に耐える現像
剤ではなかった。- Saturated polyester resin 100 parts (trade name: Polyester-HI"32θ, manufactured by Nippon Gosei Kagaku Kogyo Co., Ltd.) - Low molecular weight polypropylene 3 parts (trade name: Hiskol 5e, manufactured by Sanyo Chemical Co., Ltd.) - Charge control agent 4 parts (trade name) TP-302, manufactured by Odugaya Chemical Industry Co., Ltd.)・
C. 1. Solvent Yellow 2
Part 13 (Product name: Helifast Yellow 3120
, manufactured by Orient Kaji Kogyo Co., Ltd.) The above materials were used in Example 1. It was treated in the same manner as above to obtain a classified product with an average particle size of 11 μm. Q. Q weight%
Antimony-doped tin oxide (trade name: Tybake SN-1 00, manufactured by Ishiya Sangyo Co., Ltd.) was externally added using a Henschel mixer to obtain the yellow toner of the present invention. A developer was prepared from this toner using the same carrier as in Example 1, and the amount of triboelectric charge was measured, and it was found to be +21.0 μC'g. This toner is a positively charged toner, and this toner was used in Example 1. 20 was printed under the same conditions by modifying the Caesar printer used in 2010. Similarly, in various environments, the amount of frictional charge of the toner of the present invention showed little variation between various environments and during running. Stable results were obtained with respect to the change in triboelectric charge amount, and good print density was obtained. For comparison purposes, toner production, developer production, and testing were conducted under the same conditions as above, except that antimony-doped tin oxide was not used, and the resulting images changed significantly as the number of running sheets increased. In addition, there were large variations between environments, and the developer was not suitable for practical use.
以上のような木実施例は正帯電性、負帯電性の両方に使
用でき上記物質は淡灰色であるが透明性をもっているた
めカラートナーに対しては、好適に帯電制御効果を示し
かつ色調を損なうことのない鮮明なカラートナーを提供
することができる。The above-mentioned wood examples can be used for both positively charging and negatively charging properties.Although the above-mentioned material is pale gray, it is transparent, so it shows a suitable charge control effect and color tone for color toners. It is possible to provide clear color toner without damage.
なおトナーにアンチモンドーピング型酸化スズを含有せ
しめる形態としては、トナー中に内添せしめてもよいし
、またトナー粒子表面に外添してもよい。その配合量は
、トナー中(こ内添する場合は樹脂100重量部に対し
て、0.3〜10.0重量部の範囲が好ましく、トナー
粒子表面に外添する場合は、トナー組成100重量部に
対して0.01〜2.00重量部の範囲が好ましい。そ
れぞれ上記範囲より少ないと、トナーの摩擦帯電安定性
が損なわれ、多いと、逆に十分な帯電量を確保できなく
なる。尚、本発明の結着樹脂としては、公知のものがす
べて使用可能である。例えば、ポリスチレン、ポリ−α
−メチルスチレン、クロロポリスチレン、スチレン−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−ブタジェン共重合体、スチレン−塩化ビニ
ル共重合体、スチレン−酢酸ビニル共重合体、スチレン
−マレイン酸共重合体、スチレン−アクリル酸エステル
共重合体、スチレン−メタクリル酸エステル共重合体、
スチレン−α−クロルアクリル酸メチル共重合体、スチ
レン−アクリロニトリル−アクリル酸エステル共重合体
等のスチレン系樹脂(スチレン又はスチレン置換体を含
む単重合体又は共重合体)、エポキシ樹脂、ウレタン変
性エポキシ樹脂、シリコーン変性エポキシ樹脂、ポリエ
ステル樹脂、塩化ビニル樹脂、スチレン−酢酸ビニル共
重合体、ロジン変性マレイン酸樹脂、フェニール樹脂、
ポリエチレン、ポリプロピレン、アイオマー樹脂、ポリ
ウレタン樹脂、シリコーン樹脂、ケトン樹脂、エチレン
−エチルアクリレート共重合体、キシレン樹脂、ポリヒ
ニルブチラール樹脂、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、等か単独又は混合され
て使用できる。特に本実施例に好ましいものとしては、
スチレン−アクリル酸エステル系樹脂、スチレン−メタ
クリル酸エステル系樹脂、ポリエステル樹脂がある。ま
た、本現像剤を二成分用トナーとして使用する場合、キ
ャリアとしては公知のものが使用できる。例えば、表面
酸化または未酸化の鉄または鉄とニッケル、銅、亜鉛、
コバルト、マンガン、クロム、希土類等の金属及びそれ
らの合金、又は酸化物及びフェライトなとが使用できる
。またこれらの表面を種々の樹脂等でコーティングした
ものも使用できる。また、場合に応じて現像剤に対して
コロイダルシリカなとの流動性改質剤をトナーに対して
0.01〜6.00重量%(特に好ましくは0.1〜1
.0重量%)程度添加してもさしつかえない。Note that antimony-doped tin oxide may be contained in the toner by either internally adding it to the toner or externally adding it to the surface of the toner particles. The blending amount is preferably in the range of 0.3 to 10.0 parts by weight per 100 parts by weight of the resin in the toner (if added internally, it is preferably in the range of 0.3 to 10.0 parts by weight per 100 parts by weight of the resin, and if added externally to the toner particle surface, per 100 parts by weight of the toner composition). The amount is preferably in the range of 0.01 to 2.00 parts by weight.If it is less than the above range, the triboelectric charging stability of the toner will be impaired, and if it is more than that, it will not be possible to secure a sufficient amount of charge. As the binder resin of the present invention, all known binder resins can be used.For example, polystyrene, poly-α
- Methylstyrene, chloropolystyrene, styrene-chlorostyrene copolymer, styrene-propylene copolymer, styrene-butadiene copolymer, styrene-vinyl chloride copolymer, styrene-vinyl acetate copolymer, styrene-maleic acid copolymer polymer, styrene-acrylic ester copolymer, styrene-methacrylic ester copolymer,
Styrenic resins (styrene or styrene-substituted monopolymers or copolymers containing styrene or styrene substitutes) such as styrene-α-methyl chloroacrylate copolymer, styrene-acrylonitrile-acrylic acid ester copolymer, epoxy resin, urethane-modified epoxy Resin, silicone-modified epoxy resin, polyester resin, vinyl chloride resin, styrene-vinyl acetate copolymer, rosin-modified maleic acid resin, phenyl resin,
Polyethylene, polypropylene, iomer resin, polyurethane resin, silicone resin, ketone resin, ethylene-ethyl acrylate copolymer, xylene resin, polyhinyl butyral resin, terpene resin, phenol resin,
Aliphatic or alicyclic hydrocarbon resins can be used alone or in combination. Particularly preferable for this example are:
There are styrene-acrylic ester resins, styrene-methacrylic ester resins, and polyester resins. Furthermore, when the present developer is used as a two-component toner, known carriers can be used. For example, surface oxidized or unoxidized iron or iron and nickel, copper, zinc,
Metals such as cobalt, manganese, chromium, rare earths, alloys thereof, or oxides and ferrites can be used. Moreover, those whose surfaces are coated with various resins can also be used. Depending on the case, a fluidity modifier such as colloidal silica may be added to the developer in an amount of 0.01 to 6.00% by weight (particularly preferably 0.1 to 1% by weight) based on the toner.
.. 0% by weight) may be added.
(発明の効果)
本発明は、アンチモンがドーピングされた酸化スズ(S
n02)を添加した事により、2成分現像方式に於ける
摩擦帯電性を安定化させることかできるので、得られる
画像の品質が常に良好であり、特にカラートナーとして
非常に優れた品質を提供できるものである。所定の濃度
を保つことかでき、OPC等の感光体の表面を傷つける
こともなく、キャリア汚染のない良好なカラートナ又は
現像剤を供給することが可能となる。(Effects of the Invention) The present invention provides antimony-doped tin oxide (S).
By adding n02), it is possible to stabilize the triboelectricity in the two-component development system, so the quality of the images obtained is always good, and especially as a color toner, it can provide very excellent quality. It is something. A predetermined density can be maintained, the surface of a photoreceptor such as an OPC will not be damaged, and a good color toner or developer without carrier contamination can be supplied.
第1図は現像枚数と摩擦帯電量の関係を示す図、第2図
は現像枚数と印字濃度の関係を示す図である。
1.2.3・・・・・・線
4.5.6・・・・・・線
7.8.9・・・・・・線
10.11.12・・・・・・線FIG. 1 is a diagram showing the relationship between the number of developed sheets and the amount of triboelectric charge, and FIG. 2 is a diagram showing the relationship between the number of developed sheets and print density. 1.2.3... line 4.5.6... line 7.8.9... line 10.11.12... line
Claims (1)
ズとを含有する事を特徴とする静電潜像現像用トナー。A toner for developing electrostatic latent images characterized by containing a resin, a pigment, and tin oxide doped with antimony.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2129597A JPH0424646A (en) | 1990-05-18 | 1990-05-18 | Electrostatic latent image developing toner |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2129597A JPH0424646A (en) | 1990-05-18 | 1990-05-18 | Electrostatic latent image developing toner |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0424646A true JPH0424646A (en) | 1992-01-28 |
Family
ID=15013388
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2129597A Pending JPH0424646A (en) | 1990-05-18 | 1990-05-18 | Electrostatic latent image developing toner |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0424646A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH06118693A (en) * | 1992-10-07 | 1994-04-28 | Tomoegawa Paper Co Ltd | Non-magnetic one-component developing method |
EP0687960A1 (en) | 1994-06-14 | 1995-12-20 | Canon Kabushiki Kaisha | Toner for developing electrostatic images and image forming method |
-
1990
- 1990-05-18 JP JP2129597A patent/JPH0424646A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH06118693A (en) * | 1992-10-07 | 1994-04-28 | Tomoegawa Paper Co Ltd | Non-magnetic one-component developing method |
EP0687960A1 (en) | 1994-06-14 | 1995-12-20 | Canon Kabushiki Kaisha | Toner for developing electrostatic images and image forming method |
US5614344A (en) * | 1994-06-14 | 1997-03-25 | Canon Kabushiki Kaisha | Toner for developing electrostatic images and image forming method |
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