JPH0424652A - Negatively electrostatically charged cyan toner for color electrophotography - Google Patents
Negatively electrostatically charged cyan toner for color electrophotographyInfo
- Publication number
- JPH0424652A JPH0424652A JP2129599A JP12959990A JPH0424652A JP H0424652 A JPH0424652 A JP H0424652A JP 2129599 A JP2129599 A JP 2129599A JP 12959990 A JP12959990 A JP 12959990A JP H0424652 A JPH0424652 A JP H0424652A
- Authority
- JP
- Japan
- Prior art keywords
- pigment
- electrostatically charged
- toner
- negatively
- parts
- 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
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 31
- 239000000049 pigment Substances 0.000 claims abstract description 25
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 14
- 230000002209 hydrophobic effect Effects 0.000 claims abstract description 11
- 239000012860 organic pigment Substances 0.000 claims abstract description 7
- 239000003086 colorant Substances 0.000 claims abstract 3
- 229920005989 resin Polymers 0.000 claims description 23
- 239000011347 resin Substances 0.000 claims description 23
- 239000011230 binding agent Substances 0.000 claims description 6
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical group 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 claims description 6
- 230000032683 aging Effects 0.000 abstract 2
- 230000015556 catabolic process Effects 0.000 abstract 2
- 238000006731 degradation reaction Methods 0.000 abstract 2
- 229920001577 copolymer Polymers 0.000 description 10
- -1 chloropolystyrene Polymers 0.000 description 6
- 239000004743 Polypropylene Substances 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 229920001155 polypropylene Polymers 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 230000006866 deterioration Effects 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 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 3
- 239000003822 epoxy resin Substances 0.000 description 3
- YLGXILFCIXHCMC-JHGZEJCSSA-N methyl cellulose Chemical compound COC1C(OC)C(OC)C(COC)O[C@H]1O[C@H]1C(OC)C(OC)C(OC)OC1COC YLGXILFCIXHCMC-JHGZEJCSSA-N 0.000 description 3
- 229920000647 polyepoxide Polymers 0.000 description 3
- 229920001225 polyester resin Polymers 0.000 description 3
- 239000004645 polyester resin Substances 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
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 2
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 2
- 229910000859 α-Fe Inorganic materials 0.000 description 2
- 229910002014 Aerosil® 130 Inorganic materials 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 241000270281 Coluber constrictor Species 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
- 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
- 230000002378 acidificating effect Effects 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
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 238000004581 coalescence Methods 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
- 238000004040 coloring 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
- OQZCSNDVOWYALR-UHFFFAOYSA-N flurochloridone Chemical compound FC(F)(F)C1=CC=CC(N2C(C(Cl)C(CCl)C2)=O)=C1 OQZCSNDVOWYALR-UHFFFAOYSA-N 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 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
- 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
- 239000000463 material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229920003146 methacrylic ester copolymer Polymers 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002245 particle Substances 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
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 238000010186 staining Methods 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
- 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
この発明はカラー電子写真用負帯電性シアントナーに関
する。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention This invention relates to a negatively chargeable cyan toner for color electrophotography.
従来の技術
カラー電子写真用トナーとして、結着樹脂中に各種の染
料や顔料を分散させたトナーか広く使用されている。こ
れらのカラートナーの内、電子写真用シアントナーとし
ては、フタロシアニン系有機顔料を用いたものか、主と
して使用されている。2. Description of the Related Art Toners in which various dyes and pigments are dispersed in a binder resin are widely used as toners for color electrophotography. Among these color toners, those using phthalocyanine organic pigments are mainly used as cyan toners for electrophotography.
これは、フタロシアニン系有機顔料か鮮明な青色を有し
、単色コピーでも多色コピーでも色再現性に秀れている
からである。しかし、フタロシアニン系有機顔料は、そ
れ自身、正帯電性か強いため、負帯電性トナーでの使用
はコピー画質の劣化を招き易い。This is because phthalocyanine-based organic pigments have a clear blue color and have excellent color reproducibility in both monochrome and multicolor copies. However, since phthalocyanine organic pigments are themselves highly positively chargeable, their use in negatively chargeable toners tends to cause deterioration in copy image quality.
発明か解決しようとする課題
フタロシアニンは本質的に正に帯電する傾向を有してお
り、負帯電性トナーとして用いると、経済的に現像特性
の劣化を招き易いという欠点か認められる。Problems to be Solved by the Invention Phthalocyanine inherently has a tendency to be positively charged, and when used as a negatively chargeable toner, it is recognized that it has a disadvantage in that it tends to economically deteriorate the development characteristics.
従って、本発明は従来の負帯電性シアントナーにおける
上記欠点を解消し、優れた帯電特性、耐経時劣下性およ
び耐湿性を持つようにするものである。Therefore, the present invention eliminates the above-mentioned drawbacks of conventional negatively chargeable cyan toners and provides excellent charging characteristics, resistance to deterioration over time, and moisture resistance.
課題を解決するだめの手段
そして上記問題点を解決する本発明の技術的な手段は、
フタロシアニン系青色有機顔料の表面を負帯電性疎水シ
リカて被覆するものである。Means for solving the problems and technical means of the present invention for solving the above problems are as follows:
The surface of a phthalocyanine-based blue organic pigment is coated with negatively charged hydrophobic silica.
負帯電性疎水シリカとしては、5〜100mm、比表面
積80〜700m/ g ”!粉末二酸化ケイ素かよい
。この微粉末としては、アエロジル130 、2003
00 、 380 、 0x50. TT600 、
MOx80゜MOx170 、 C0K84R9
72、R812(以上日本アエロジル■製)のようなも
のかある。The negatively charged hydrophobic silica may be powdered silicon dioxide with a size of 5 to 100 mm and a specific surface area of 80 to 700 m/g. As for this fine powder, Aerosil 130, 2003
00, 380, 0x50. TT600,
MOx80゜MOx170, C0K84R9
72, R812 (manufactured by Nippon Aerosil ■).
C.I.ピグメント・ブルー15−3に属する顔料とし
ては、シアニンブルー4938 (大日精化■製)、モ
ナストラル・ブルーBG(ICIIm製)、ホスタベル
ム・ブルーBG(日本ヘキスト■製)、スミカブリント
・シアニン・ブルーGN−0−3(住人化学@り 、リ
オノール・ブルーGLA(東洋インキ■製)、KETブ
ルー104、KETブルーII+ (大日本インキ■製
)なとかあげられる。顔料の表面をシリカで被覆する方
法はヘンノニルミキサやスーパーミキサに顔料:シリカ
=+00:0,1〜100 : 10の重量比でより好
ましくは100 : 3〜100ニアて仕込み、高速回
転により行う。C. I. Pigments belonging to Pigment Blue 15-3 include Cyanine Blue 4938 (manufactured by Dainichiseika), Monastral Blue BG (manufactured by ICIIm), Hostaverum Blue BG (manufactured by Nippon Hoechst), Sumikablint Cyanine Blue GN- Examples include 0-3 (Sumiman Kagaku@ri), Lionor Blue GLA (manufactured by Toyo Ink ■), KET Blue 104, and KET Blue II+ (manufactured by Dainippon Ink ■).The method of coating the surface of the pigment with silica is strange. Pigment:silica = +00:0, weight ratio of 1 to 100:10, preferably 100:3 to 100, is charged into a nonyl mixer or super mixer, and the mixture is rotated at high speed.
本発明に使用する上記顔料の添加量は、樹脂100重量
部に対して0,1〜10.0重量部か望ましい。The amount of the pigment used in the present invention is preferably 0.1 to 10.0 parts by weight per 100 parts by weight of the resin.
更に望ましくは2.0〜4.0重量部である。0.1重
量部以下であると発色特性か得られず十分な画像濃度か
確保てきなくなり、10重量部以上であると顔料の樹脂
に対する分散が低下し、帯電特性か劣下する。More preferably, the amount is 2.0 to 4.0 parts by weight. If the amount is less than 0.1 parts by weight, coloring properties cannot be obtained and sufficient image density cannot be secured, and if it is more than 10 parts by weight, the dispersion of the pigment in the resin will be reduced and the charging characteristics will be deteriorated.
トナーの帯電制御は、結着樹脂、顔料自体で行ってもよ
いか、必要に応して色再現上問題の生しないような帯電
制置剤を併用してもよい。例えは、含金染料等の金属キ
レート類、酸性もしくは電子吸引性の有機物質等と用い
ることか出来る。The charge control of the toner may be performed using the binder resin or pigment itself, or, if necessary, a charge control agent that does not cause problems in color reproduction may be used in combination. For example, metal chelates such as gold-containing dyes, acidic or electron-withdrawing organic substances, etc. can be used.
なお、本発明の結着樹脂としては、公知のものかすへて
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−
エチル了クリレート共重合体、キシレン樹脂、ポリビニ
ルブチラール樹脂、テルペン樹脂、フェノール樹脂、脂
肪族又は指環族炭化水素樹脂、等か単独又は混合されて
使用できる。特に本事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、ポリエステル樹脂かある。Note that any known binder resin can be used as the binder resin of the present invention. For example, polystyrene, poly-α-methylstyrene, chloropolystyrene, styrene-chlorostyrene copolymer, styrene-propylene copolymer, styrene-butadiene copolymer, styrene-vinyl chloride copolymer, styrene-vinyl acetate copolymer Coalescence, styrene-maleic acid copolymer, styrene-acrylic ester copolymer, styrene-methacrylic ester copolymer, styrene-α-methyl chloroacrylate copolymer, styrene-acrylonitrile-acrylic ester copolymer Styrenic resins (unipolymers or copolymers containing styrene or styrene substitutes), epoxy resins, urethane-modified resins, etc.
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 copolymers, xylene resins, polyvinyl butyral resins, terpene resins, phenol resins, aliphatic or ring hydrocarbon resins, etc. can be used alone or in combination. Particularly preferred in this case are styrene-acrylic ester resins, styrene-methacrylic ester resins, and polyester resins.
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か使用できる。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か使用でき
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、必要に応じてコロイダルシ
リカなとの流動性改質剤をトナーに対して0.01〜6
.000重量部(より好ましくは0.1〜1.0重量0
6)添加してもよい。In addition, when using this developer as a two-component toner,
Any known carrier can be used. For example, surface-oxidized or unoxidized iron or iron and metals such as nickel, copper, zinc, cobalt, manganese, chromium, rare earths, and alloys thereof, or oxides and ferrites can be used. Moreover, those whose surfaces are coated with various resins can also be used. In addition, if necessary, a fluidity modifier such as colloidal silica may be added to the toner in an amount of 0.01 to 6.
.. 000 parts by weight (more preferably 0.1 to 1.0 parts by weight)
6) May be added.
作用 この技術的手段による作用は次のようになる。action The effect of this technical means is as follows.
即ち、負帯電性疎水シリカで顔料の表面を被覆すること
により、顔料自体か持っている正電荷を中和、あるいは
顔料を負側に帯電させる。そして、トナーの極性と合致
させ、逆帯電トナーの発生を防ぐ。That is, by coating the surface of the pigment with negatively charged hydrophobic silica, the positive charge that the pigment itself has is neutralized or the pigment is charged negatively. Then, the polarity is matched with that of the toner to prevent generation of oppositely charged toner.
また、シリカか疎水性であるため、高湿条件下において
も良好な耐湿性を有する。よって結果として優れた帯電
特性と耐経時劣下性を持つようになるのである。Furthermore, since silica is hydrophobic, it has good moisture resistance even under high humidity conditions. As a result, it has excellent charging characteristics and resistance to deterioration over time.
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。な
お、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へて重量部数で
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. In the following, 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 100部(商
品名 ハイマーTBL−500.三洋化成社製)・ポリ
プロピレンワックス 4部(商品名 ビ
スコール550−P、三洋化成社製)・帯電制御剤
4部(商品名 カヤチャージ
N−31日本化薬社製)・C.I.ピグメント・ブルー
15−3 3部上記材料を、ヘンシェルミキサーて
均一に分散し、分散物を2軸押量機等で溶融混練し、冷
却後ジェットミル等で微粉砕し、分級機にて平均粒径1
1umの分級品を得た。この分級品に0.3%の疎水性
シリカ(商品名 R972,日本アエロジル社製)をヘ
ンシェルミキサーで外添し、本発明のシアントナーを得
た。このトナーをフェライトキャリア(PL−150,
日本鉄粉社製)と混合し、現像剤とした。この現像剤を
用いてレーサープリンター(商品名 K X −P 4
450.松下電器社製)で連続20、000枚印産金行
った。得られたプリント物の画像品質は1〜20.00
0枚を通して良好であった。Example 1゜・Styrene-acrylic acid ester resin 100 parts (trade name Hymer TBL-500, manufactured by Sanyo Chemical Co., Ltd.)・Polypropylene wax 4 parts (trade name Viscole 550-P, manufactured by Sanyo Chemical Co., Ltd.)・Charge control agent
4 parts (product name Kaya Charge N-31 manufactured by Nippon Kayaku Co., Ltd.)・C. I. Pigment Blue 15-3 3 parts The above materials are uniformly dispersed using a Henschel mixer, the dispersion is melt-kneaded using a twin-screw extruder, etc., and after cooling, it is finely pulverized using a jet mill, etc., and the average particle size is averaged using a classifier. Diameter 1
A 1 um classified product was obtained. To this classified product, 0.3% hydrophobic silica (trade name R972, manufactured by Nippon Aerosil Co., Ltd.) was externally added using a Henschel mixer to obtain the cyan toner of the present invention. Transfer this toner to a ferrite carrier (PL-150,
(manufactured by Nippon Tetsuko Co., Ltd.) to form a developer. Using this developer, you can print a racer printer (product name: KX-P4).
450. Manufactured by Matsushita Electric Co., Ltd.), 20,000 coins were produced in a row. The image quality of the obtained print is 1 to 20.00.
It was good through all 0 sheets.
実施例2゜
・スチレン−アクリル酸エステル系樹脂 100部(ハ
イマー T B −1000三洋化成■製)・ポリプロ
ピレンワックス 4部(ビスコール 5
50−P 三洋化成■製)・帯電制御剤
4部(カヤチャージ N−3日本化薬
味製)・C.I.ピグメント・ブルー15−3 3
部上記顔料に対して3%の負帯電性疎水シリカで表面被
覆しである。Example 2゜・Styrene-acrylic acid ester resin 100 parts (Himer TB-1000 manufactured by Sanyo Chemical Co., Ltd.)・Polypropylene wax 4 parts (Viscol 5 parts)
50-P (manufactured by Sanyo Chemical)・Charge control agent
4 parts (Kaya Charge N-3 manufactured by Nippon Kajimi)・C. I. Pigment Blue 15-3 3
The surface is coated with 3% negatively charged hydrophobic silica based on the above pigment.
実施例1と同様にしてシアントナー得た。また、同様の
印字試験を行った。これも1〜20.000ffを通し
て、良好な印字品質であった。A cyan toner was obtained in the same manner as in Example 1. A similar printing test was also conducted. This also had good print quality throughout the range of 1 to 20,000 ff.
比較例1゜
・スチレン−アクリル酸エステル系樹脂 100部(ハ
イマーT B −1000三洋化成■製)・ポリプロピ
レンワックス 4部(ビスコール55
0−P 三洋化成■製)・帯電制御剤
4部(カヤチャージ N−3日本化薬味
製)・C.I.ピグメント・ブルー15−3 3部
(KET Blue −104大日本インキ■製)実
施例1.と同様の方法でシアントナーを得た。Comparative Example 1°・100 parts of styrene-acrylic acid ester resin (Himer T B-1000 manufactured by Sanyo Chemical Co., Ltd.)・4 parts of polypropylene wax (Viscol 55
0-P (manufactured by Sanyo Chemical)・Charge control agent
4 parts (Kaya Charge N-3 manufactured by Nippon Kajimi)・C. I. Pigment Blue 15-3 3 parts (KET Blue-104 manufactured by Dainippon Ink ■) Example 1. A cyan toner was obtained in a similar manner.
また、同様の印字試験を行った。7.000枚程産生て
は良好な印字品質てあったか、13.000枚程産生ら
は非画像部の汚れか目立つようになり、20.000枚
後では使用に耐えない印字品質となった。これは、顔料
かトナーと逆の帯電性を持つことに起因すると考えられ
る。即ち、逆帯電トナーの割合か、印字とともに増加し
、これか非画像部汚れの原因と考えられる。A similar printing test was also conducted. After about 7,000 sheets were produced, the print quality was good, but after about 13,000 sheets, dirt became noticeable in the non-image area, and after 20,000 sheets, the print quality became unusable. This is considered to be due to the fact that the pigment has a chargeability opposite to that of the toner. That is, the ratio of the oppositely charged toner increases with printing, and this is thought to be the cause of the staining of the non-image area.
比較例2゜
・ポリエステル樹脂 100部(
ハイマーES−508三洋化成■製)・ポリプロピレン
ワックス 4部(ビスコール550−P
三洋化成■製)・帯電制御剤
4部(カヤチャージ N−3日本化薬味製)・
C.I.ピグメント・ブルー15−3 3部(KE
T B ] u e −III 大日本インキ■製
)実施例1.と同様の方法でシアントナーを得た。Comparative Example 2゜・100 parts of polyester resin (
Hymer ES-508 (manufactured by Sanyo Chemical), 4 parts polypropylene wax (Viscol 550-P
Manufactured by Sanyo Chemical Co., Ltd.) / Charge control agent
4 parts (Kaya Charge N-3 made by Nippon Kakami)・
C. I. Pigment Blue 15-3 3 parts (KE
TB]ue-III Manufactured by Dainippon Ink ■) Example 1. A cyan toner was obtained in a similar manner.
また、同様の印字試験を行った。印字枚数5.000枚
程産生では良好な印字品質であったか、10.000枚
程産生らは非画像部の汚れか目立つようになり、20、
000枚後では使用に耐えない印字品質となった。A similar printing test was also conducted. The print quality was good when printing about 5,000 sheets, but when printing about 10,000 sheets, dirt became noticeable in the non-image area.
After 1,000 sheets, the print quality became unusable.
これも、逆帯電トナーの増加によると考えられる。This is also considered to be due to an increase in the amount of oppositely charged toner.
発明の効果
以上、説明したように、本発明のシアントナーを用いる
ことにより、逆帯電トナーの発生を押さえ、優れた帯電
特性、耐経時劣下性および耐湿性を有する負帯電性トナ
ーを得ることがてきる。よって、長期にわたり、印字品
質の良好なシアン色の画像を提供できる。Effects of the Invention As described above, by using the cyan toner of the present invention, it is possible to suppress the generation of reversely charged toner and obtain a negatively charged toner having excellent charging characteristics, resistance to deterioration over time, and resistance to moisture. It's coming. Therefore, a cyan image with good print quality can be provided for a long period of time.
また、本発明の顔料を用いると、負帯電性−成分シアン
トナーとしても広く使用する事か可能になる。Furthermore, the pigment of the present invention can be widely used as a negatively chargeable component cyan toner.
Claims (3)
が負帯電性疎水シリカで表面を被覆されたフタロシアニ
ン系青色有機顔料である事を特徴とするカラー電子写真
用負帯電性シアントナー。(1) A negatively chargeable cyan toner for color electrophotography, which contains a colorant and a binder resin as main components, and the colorant is a phthalocyanine-based blue organic pigment whose surface is coated with negatively chargeable hydrophobic silica. .
に分類される特許請求の範囲第1項記載のトナー。(2) The pigment is C.I. I. pigment blue 15-3
The toner according to claim 1, which is classified as:
割合で含有される特許請求の範囲第1項記載のトナー。(3) The toner according to claim 1, wherein the pigment is contained in a proportion of 0.5 to 10% by weight based on the binder resin.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2129599A JP2805975B2 (en) | 1990-05-18 | 1990-05-18 | Negatively chargeable cyan toner for color electrophotography |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2129599A JP2805975B2 (en) | 1990-05-18 | 1990-05-18 | Negatively chargeable cyan toner for color electrophotography |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0424652A true JPH0424652A (en) | 1992-01-28 |
JP2805975B2 JP2805975B2 (en) | 1998-09-30 |
Family
ID=15013439
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2129599A Expired - Fee Related JP2805975B2 (en) | 1990-05-18 | 1990-05-18 | Negatively chargeable cyan toner for color electrophotography |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2805975B2 (en) |
-
1990
- 1990-05-18 JP JP2129599A patent/JP2805975B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JP2805975B2 (en) | 1998-09-30 |
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