JPH02267565A - Positive chargeable toner - Google Patents
Positive chargeable tonerInfo
- Publication number
- JPH02267565A JPH02267565A JP1089207A JP8920789A JPH02267565A JP H02267565 A JPH02267565 A JP H02267565A JP 1089207 A JP1089207 A JP 1089207A JP 8920789 A JP8920789 A JP 8920789A JP H02267565 A JPH02267565 A JP H02267565A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- charge control
- control agent
- toner
- developer
- 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
- 229920005989 resin Polymers 0.000 claims abstract description 36
- 239000011347 resin Substances 0.000 claims abstract description 36
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 27
- 239000003086 colorant Substances 0.000 claims abstract description 17
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 3
- 150000001875 compounds Chemical class 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract description 6
- 239000003822 epoxy resin Substances 0.000 abstract description 6
- 229920000647 polyepoxide Polymers 0.000 abstract description 6
- 239000006229 carbon black Substances 0.000 abstract description 4
- 239000011230 binding agent Substances 0.000 abstract description 3
- 230000006866 deterioration Effects 0.000 abstract description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 abstract 4
- 235000019241 carbon black Nutrition 0.000 abstract 1
- DCYOBGZUOMKFPA-UHFFFAOYSA-N iron(2+);iron(3+);octadecacyanide Chemical compound [Fe+2].[Fe+2].[Fe+2].[Fe+3].[Fe+3].[Fe+3].[Fe+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] DCYOBGZUOMKFPA-UHFFFAOYSA-N 0.000 abstract 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 abstract 1
- 239000004645 polyester resin Substances 0.000 description 12
- 229920001225 polyester resin Polymers 0.000 description 12
- 239000000203 mixture Substances 0.000 description 7
- 239000002245 particle Substances 0.000 description 7
- 238000009472 formulation Methods 0.000 description 6
- 239000000843 powder Substances 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 239000010419 fine particle Substances 0.000 description 3
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 3
- 239000006247 magnetic powder Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 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 2
- 238000000034 method Methods 0.000 description 2
- 108091008695 photoreceptors Proteins 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 2
- 238000010186 staining Methods 0.000 description 2
- 229910000859 α-Fe Inorganic materials 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N 1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid Chemical compound C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- VOZKAJLKRJDJLL-UHFFFAOYSA-N 2,4-diaminotoluene Chemical compound CC1=CC=C(N)C=C1N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- CJPQIRJHIZUAQP-MRXNPFEDSA-N benalaxyl-M Chemical compound CC=1C=CC=C(C)C=1N([C@H](C)C(=O)OC)C(=O)CC1=CC=CC=C1 CJPQIRJHIZUAQP-MRXNPFEDSA-N 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 230000005389 magnetism Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 239000012860 organic pigment 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
- 229920000728 polyester Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 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)
本発明は電子写真等の分野に用いられる正帯電性トナー
に関する。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a positively chargeable toner used in fields such as electrophotography.
(従来の技術と解決すべき問題点)
従来より電子写真感光体などの潜像保持面上に形成され
る静電荷像を現像するための現像剤としては、キャリア
とトナーとからなる二成分系現像剤及びキャリアを必要
としない一成分現像剤(磁性トナー)が知られている。(Prior art and problems to be solved) Conventionally, two-component developers consisting of carrier and toner have been used as developers for developing electrostatic images formed on latent image holding surfaces such as electrophotographic photoreceptors. A one-component developer (magnetic toner) that does not require a developer or a carrier is known.
これらの現像剤を構成するトナー粒子は通常、樹脂1着
色剤、荷電制御剤等を成分とする着色微粒子である。−
成分系現像剤においては、着色剤として磁性を有するマ
グネタイト等の磁性微粒子を用いる。The toner particles constituting these developers are usually colored fine particles containing a resin 1 colorant, a charge control agent, etc. as components. −
In component-based developers, magnetic fine particles such as magnetite having magnetism are used as colorants.
これらトナーにおける樹脂成分としてはスチレン系樹脂
、エポキシ系樹脂、ポリエステル系樹脂などの公知のも
のが使用できる。As the resin component in these toners, known resins such as styrene resin, epoxy resin, and polyester resin can be used.
しかしながら低温定着性、耐塩化ビニル汚染性に優れた
エポキシ系樹脂、ポリエステル系樹脂中にニグロシン等
の染料を荷電制御剤として含有せしめた正荷電性トナー
とした現像剤を普通紙複写機、プリンターなどで繰り返
し用いる場合実用上、以下の問題点が生じる。However, developers using positively charged toners containing dyes such as nigrosine as a charge control agent in epoxy resins and polyester resins, which have excellent low temperature fixability and resistance to vinyl chloride staining, are used in plain paper copiers, printers, etc. In practice, the following problems arise when using the device repeatedly.
(イ)樹脂固有の帯電性がOH基、C0OH基を持つた
め負帯電性でl)摩擦帯電性が不均一となり、しかもキ
ャリアとの混合によシ経時的に不安定な摩擦帯電特性と
なる。この不拘、不安定のため画像濃度の不足、カブリ
の悪化等の種々の画像欠陥を生じやすい。(a) The inherent chargeability of the resin has OH groups and COOH groups, so it is negatively chargeable.l) The triboelectricity becomes uneven, and furthermore, when mixed with a carrier, the triboelectricity becomes unstable over time. . This inconsistency and instability tend to cause various image defects such as insufficient image density and worsening of fog.
(ロ)現像されたトナー粒子が紙などに有効に転写され
る割合、すなわち転写効率が低く見られる画像がムラや
カスレを生じやすい。(b) The rate at which developed toner particles are effectively transferred to paper or the like, that is, the transfer efficiency is low, and images tend to be uneven or faded.
(ハ) キャリアとの混合による経時的不安定な摩擦帯
電特性のため現像剤の抵抗が変化し諧調性、解像度等の
画質が変化する。(c) Due to the triboelectric charging characteristics that are unstable over time due to mixing with carrier, the resistance of the developer changes and image quality such as gradation and resolution changes.
(問題点を解決するための手段)
本発明者らは上述した従来のトナーの問題点を解消し、
諸要求特性を満足するトナーを得るべく鋭意検討した結
果、トナー粒子側々の摩擦帯電性が経時的にも均一安定
であって現像剤の抵抗変化の少ない、しかも良好な転写
性を有した正帯電性トナーを見い出し、本発明に到達し
た。(Means for Solving the Problems) The present inventors solved the problems of the conventional toner described above,
As a result of intensive studies to obtain a toner that satisfies various required characteristics, we have developed a positive toner that has uniform and stable triboelectric charging properties on each side of the toner particles over time, little change in resistance of the developer, and good transferability. We discovered a chargeable toner and arrived at the present invention.
すなわち、本発明の要旨は少なくとも樹脂、着色剤およ
び荷電制御剤からなるトナーにおいて、該荷電制御剤が
少なくとも下記一般式で表わせるトリアミノトリフェニ
ルメタン系化合物を樹脂700重量部に対して0.0!
〜/Q重量部含有せしめたことを特徴とする正荷電性ト
ナーに存する。That is, the gist of the present invention is to provide a toner consisting of at least a resin, a colorant, and a charge control agent, in which the charge control agent contains at least a triaminotriphenylmethane compound represented by the following general formula, based on 700 parts by weight of the resin. 0!
~/Q parts by weight of a positively charged toner.
(Rは炭素数/−jのアルキル基を表わす。)以下、本
発明の詳細な説明する。(R represents an alkyl group having carbon number/-j.) The present invention will be described in detail below.
本発明のトナーにおける着色剤としては各種公知の着色
剤が使用できる。例えば、カーボンブラック、紺青、酸
化チタン等の無機顔料、アゾ系、フタロシアニン系等の
有機顔料、及びアントラキノン系等の染料が挙げられる
。これらは鮮明な可視像を得るのに必要な量をトナー中
に含有させるが、通常、樹脂100重量部に対して20
重量部以下、好ましくは10重量部以下である。Various known colorants can be used as the colorant in the toner of the present invention. Examples include inorganic pigments such as carbon black, navy blue, and titanium oxide, organic pigments such as azo pigments and phthalocyanine pigments, and dyes such as anthraquinone pigments. These are contained in the toner in the amount necessary to obtain a clear visible image, but usually 20 parts by weight per 100 parts by weight of the resin.
It is not more than 10 parts by weight, preferably not more than 10 parts by weight.
本発明で使用するバインダー樹脂は公知のスチレン系樹
脂、エポキシ系樹脂及びポリエステル系樹脂が使用でき
、これらの樹脂の熱特定は定着特性、保存特性等のトナ
ーの要求される熱的な性能を満足することが必要である
。これらは架橋剤によって架橋されていても良い。Known styrene resins, epoxy resins, and polyester resins can be used as the binder resin used in the present invention, and the thermal properties of these resins satisfy the thermal performance required of toners such as fixing properties and storage properties. It is necessary to. These may be crosslinked with a crosslinking agent.
本発明においては、特にエポキシ系樹脂及び/又は酸価
がjKOH/g9以下のポリエステル系樹脂をバインダ
ー樹脂とすることが好ましく、この樹脂の酸価がjKO
H/WIgよシ高いと樹脂自体の負荷電性が強くなり、
正荷電性制御剤を添加しても十分な正帯電特性が得られ
ない。かかる樹脂を用いた本発明のトナーは使用する特
定の荷電制御剤との結合において、優れた帯電特性が得
られると共に1耐塩化ビニル汚染性に優れ、この意味で
プリンター用のトナーとして特に好適である。In the present invention, it is particularly preferable to use an epoxy resin and/or a polyester resin having an acid value of jKOH/g9 or less as the binder resin;
When H/WIg is higher, the negative chargeability of the resin itself becomes stronger,
Even if a positive charge control agent is added, sufficient positive charge characteristics cannot be obtained. The toner of the present invention using such a resin has excellent charging properties when combined with the specific charge control agent used, and has excellent resistance to vinyl chloride staining, and in this sense, it is particularly suitable as a toner for printers. be.
本発明に使用する荷電制御剤は必須成分として前述した
一般式のトリアミノトリフェニルメタン系化合物(以下
、TAPM化合物と言う)を用いるが、その他ニグロシ
ン系染料、四級アンモニウム塩などの公知の正荷電性制
御剤をトナーの帯電特性を乱さない範囲で併用しても良
いO
荷電制御剤の添加量は樹脂100重量部に対して0.0
1〜10重量部、好ましくは0.1〜7重量部である。The charge control agent used in the present invention uses a triaminotriphenylmethane compound (hereinafter referred to as a TAPM compound) of the general formula described above as an essential component, but other known charge control agents such as nigrosine dyes and quaternary ammonium salts are also used. A charge control agent may be used in combination as long as it does not disturb the charging characteristics of the toner.The amount of charge control agent added is 0.0 parts by weight per 100 parts by weight of the resin.
The amount is 1 to 10 parts by weight, preferably 0.1 to 7 parts by weight.
また、必須成分であるTAPM化合物の添加量は樹脂1
00重量部に対して0、θj −70重量部、好ましく
は0./ −j重量部である。In addition, the amount of added TAPM compound, which is an essential component, is 1/1 of the resin.
0, θj -70 parts by weight, preferably 0.00 parts by weight. / -j parts by weight.
その他、本発明の正帯電性トナーの構成成分としては、
例えば、定着性を向上させる為に低分子量オレフィン重
合体、TiO2,A12os +5i02 + Fe5
O4等の超微粒子粉末などの、各種の内部或いは外部の
添加剤を含ませても良いが、これらは本発明の目的を阻
害しない程度とすべきである。Other constituent components of the positively chargeable toner of the present invention include:
For example, to improve fixing properties, a low molecular weight olefin polymer, TiO2, A12os +5i02 + Fe5
Various internal or external additives may be included, such as ultrafine powders such as O4, but these should be in amounts that do not interfere with the objectives of the invention.
また、トナーの製造法としては、上記の各成分を配合、
混合してニーダ−等で混練し、冷却後粉砕、分級し、必
要に応じて攪拌機等による外部添加を行なえば良い。ト
ナーの体積平均粒径としてはコールタ−カウンター測定
値で5〜20μmが好適である。In addition, the method for manufacturing toner is to combine each of the above ingredients,
They may be mixed and kneaded using a kneader or the like, cooled, then pulverized and classified, and if necessary external addition may be performed using a stirrer or the like. The volume average particle diameter of the toner is preferably 5 to 20 μm as measured by a Coulter counter.
本発明のトナーをキャリアと混合して二成分系現像剤と
して用いる場合には、キャリアとしては鉄粉、フェライ
ト粉、マグネタイト粉等が挙げられ、いずれも好適に使
用できる。また、連続使用時の耐久性向上等を目的とし
て、各種の樹脂等でコーティングした、所謂コーティン
グキャリアであっても良い。キャリアの平均粒径は10
−20θμmが好ましい。キャリアとトナーの混合重量
比は、100’、/〜/θが好適である。When the toner of the present invention is mixed with a carrier and used as a two-component developer, examples of the carrier include iron powder, ferrite powder, magnetite powder, etc., and any of them can be suitably used. Furthermore, it may be a so-called coated carrier coated with various resins for the purpose of improving durability during continuous use. The average particle size of the carrier is 10
-20θμm is preferred. The mixed weight ratio of carrier and toner is preferably 100', / to /θ.
本発明のトナーを磁性体粉末を内部に含有した一成分系
現像剤として使用する場合には、磁性体粉末としては微
粒子のマグネタイト粉、フェライト粉等が挙げられ、ト
ナー中の磁性体粉末の量はlθ〜ro重量%で、好まし
くは20〜70重量%である。When the toner of the present invention is used as a one-component developer containing magnetic powder inside, examples of the magnetic powder include fine particles of magnetite powder, ferrite powder, etc., and the amount of magnetic powder in the toner is is lθ to ro% by weight, preferably 20 to 70% by weight.
以下、実施例によシ本発明を更に詳細に説明するが、本
発明の要旨を超えない限シ以下の実施例に限定されるも
のではない。尚、実施例中「部」は「重量部」を示す。Hereinafter, the present invention will be explained in more detail with reference to examples, but the present invention is not limited to the following examples as long as the gist of the present invention is not exceeded. In addition, "parts" in the examples indicate "parts by weight."
また、帯電量はフローオツ帯電量測定装置を用いて測定
した。Further, the amount of charge was measured using a flow-on charge amount measuring device.
(実施例り
トナー原材料を下達の配合比でもって混合し、押出しニ
ーダーにより混練し、冷却後粉砕、分級し、更に分級ト
ナー700部に対して疎水性シリカ03−2部を高速攪
拌して分散せしめて平均粒径/2,3μmのトナーAを
得た。(Example) Toner raw materials were mixed at the following blending ratio, kneaded using an extrusion kneader, cooled, pulverized, and classified. Furthermore, 03-2 parts of hydrophobic silica was added to 700 parts of the classified toner and dispersed by stirring at high speed. At the very least, toner A having an average particle size of 2.3 μm was obtained.
樹 脂 ポリエステル樹脂A too
部着 色 剤 三菱カーボンプラ、り#ダθ 5
部(三菱化成■製)
帯電制御剤 コピーブルーPR2部
(ヘキスト社製)
ポリエステル樹脂AはビスフェノールA及びテレフタル
酸を主成分とするポリエステルで樹脂酸価がo、yKO
H/’n9であり、この酸価は試料を溶解する溶剤とし
てトルエンとメタノールを体積比率9:lで混合したも
のを用いた以外はJIs K−69θlK準じて測定し
九〇なお、コピーブルーPRはRがメチル基であるTA
MP化合物である。Resin Polyester resin A too
Part coloring agent Mitsubishi carbon plastic, resin #da θ 5
Part (manufactured by Mitsubishi Kasei) Charge control agent Copy Blue PR Part 2 (manufactured by Hoechst) Polyester resin A is a polyester whose main components are bisphenol A and terephthalic acid, and the resin acid value is o, yKO.
H/'n9, and this acid value was measured according to JIs K-69θlK, except that a mixture of toluene and methanol at a volume ratio of 9:1 was used as the solvent for dissolving the sample. is TA where R is a methyl group
It is an MP compound.
そして、トナーA2部と平均粒径100μmの球状鉄粉
キャリアタ♂部とを混合して“現像剤A“を調整し、セ
レン感光体を装着した反転現像方式のノンインパクトプ
リンターで連続印字テストを行なった。Then, "Developer A" was prepared by mixing two parts of toner A and a part of spherical iron powder carrier with an average particle size of 100 μm, and a continuous printing test was performed using a reversal development type non-impact printer equipped with a selenium photoreceptor. I did it.
その結果、初期からlO万ページにわたって画質の変化
がほとんどなく、また帯電量も第1表に示す様に変動は
極めて少なかった。As a result, there was almost no change in image quality from the initial stage to 10,000 pages, and as shown in Table 1, there was very little variation in the amount of charge.
(実施例2)
樹 脂 ポリエステル樹脂k 100
部着 色 剤 三菱カーボンブラック#グθ を
部帯電制御剤 コピーブルーPR/部
ポントロンN−///部
(オリエント化学工業■製)
の配合とした以外はトナーA及び現像剤Aと同様な方法
でもつってトナーB及び現像剤Bを調整し、印字テスト
した結果を第1表に示す。(Example 2) Resin Polyester resin k 100
The same method as toner A and developer A was used, except that the coloring agent Mitsubishi Carbon Black #gθ was mixed with the charge control agent Copy Blue PR/Pontron N- (manufactured by Orient Chemical Industry ■). Table 1 shows the results of a printing test after adjusting toner B and developer B.
その結果、初期から10万ページにわたって画質の変化
がほとんどなく、帯電量も初期に僅か増加したが比較的
変動は少なかった。As a result, there was almost no change in image quality from the initial stage to 100,000 pages, and although the amount of charge increased slightly at the beginning, the fluctuation was relatively small.
(実施例3)
樹 脂 ポリエステル樹脂A I00
部着 色 剤 三菱カーボンブラックnto
s部帯電制御剤 コピーブルーPRJ、を部ボントロ
ン))−4/ 0,6部(オリエント化学
工業■製)
ボントロンP−j/は四級アンモニウム塩の帯電制御剤
である。(Example 3) Resin Polyester resin A I00
Part coloring agent Mitsubishi carbon black nto
S-part charge control agent Copy Blue PRJ, Bontron)-4/0.6 parts (manufactured by Orient Chemical Industry Co., Ltd.) Bontron P-j/ is a quaternary ammonium salt charge control agent.
上記配合とした以外はトナーA及び現像剤Aと同様な方
法でもつってトナーC及び現像剤Cを調整し、印字テス
トした結果を第1表に示す。Table 1 shows the results of a printing test using toner C and developer C prepared in the same manner as toner A and developer A except for the above formulation.
その結果、初期からlO万ページにわたって画質の変化
がほとんどなく、帯電量も初期に少こし低下したが比較
的変動は少なかった。As a result, there was almost no change in image quality from the initial stage to 10,000 pages, and although the amount of charge decreased slightly at the beginning, the fluctuation was relatively small.
(実施例4t)
樹 脂 ポリエステル樹脂A ioo
部着 色 剤 三菱カーボンブラック@410
J一部帯電制御剤 コピーブルーPR/部
ボントロンN−///部
ボントロンP−t/ 0.j部上記配合と
した以外はトナーA及び現像剤Aと同様な方法でもつっ
てトナーD及び現像剤りを調整し、印字テストした結果
を第1表に示す。(Example 4t) Resin Polyester resin A ioo
Part coloring agent Mitsubishi carbon black @410
J Part Charge Control Agent Copy Blue PR/Part Bontron N-///Part Bontron P-t/ 0. Part J: Toner D and developer were adjusted in the same manner as Toner A and Developer A except for the above formulation, and a printing test was conducted. The results are shown in Table 1.
その結果、初期から10万ページにわたって画質の変化
がほとんどなく、帯電量も初期から極めて変動は少なか
った。As a result, there was almost no change in image quality over 100,000 pages from the beginning, and the amount of charge also showed very little variation from the beginning.
(実施例り
樹 脂 エポキシ樹脂;エピコート1007/
θθ部
着 色 剤 三菱カーボンブラック@4tOj部帯電
制御剤 コピーブルーPR/部
ポントロンN−090,!部
上記配合とした以外はトナーA及び現像剤Aと同様な方
法でもつってトナーE及び現像剤Eを調整し、印字テス
トした結果を第1表に示す。(Example resin epoxy resin; Epicoat 1007/
θθ part coloring agent Mitsubishi carbon black @4tOj part charge control agent Copy Blue PR/part Pontron N-090,! Table 1 shows the results of a printing test using toner E and developer E prepared in the same manner as toner A and developer A except for the above formulation.
その結果、初期から10万ベージにわたって画質の変化
がほとんどなく、帯電量も初期から比較的変動は少なか
った。As a result, there was almost no change in image quality over 100,000 pages from the initial stage, and there was also relatively little variation in the amount of charge from the initial stage.
(比較例1)
樹 脂 ポリエステル樹脂A I00
部着 色 剤 三菱カーボンブラック@/IO!部帯
電制御剤 ボントロンN−/7 2部上記
配合とした以外はトナーA及び現像剤Aと同様な方法で
もつってトナーF及び現像剤Fを調整し、印字テストし
た結果を第2表に示す。(Comparative example 1) Resin Polyester resin A I00
Part Coloring Agent Mitsubishi Carbon Black @/IO! Charge control agent Bontron N-/7 2 parts Toner F and developer F were prepared in the same manner as toner A and developer A except for the above formulation, and the results of a printing test are shown in Table 2. .
その結果、初期の画質は良好であったが、帯電量が経時
的に上昇傾向にあり、それに伴い印字濃度も徐々に低下
し、ボイドも悪化した。As a result, although the initial image quality was good, the amount of charge tended to increase over time, and accordingly, the print density gradually decreased and voids also worsened.
(比較例2)
樹 脂 ポリエステル樹脂A /θθ
部着 色 剤 三菱カーボンブラ、り@4tOj部帯
電制御剤 ボントロンN−09、、Z部上記配合とし
た以外はトナーA及び現像剤Aと同様な方法でもつって
トナーG及び現像剤Gを調整し、印字テストした結果を
第2表に示す。(Comparative Example 2) Resin Polyester resin A /θθ
Part Coloring agent: Mitsubishi Carbon Bra, Ri@4tOj Part: Charge control agent: Bontron N-09, Z part: Toner G and developer G were adjusted in the same manner as toner A and developer A, except for the above formulation. The results of the printing test are shown in Table 2.
その結果、初期の画質は良好であったが、帯電量が経時
的に低下傾向にあり、それに伴いカプリが徐々に悪化し
た。As a result, although the initial image quality was good, the amount of charge tended to decrease over time, and the capri gradually deteriorated accordingly.
(比較例3)
樹 脂 ポリエステル樹脂A ioθ
部着 色 剤 三菱カーボンプラ、り#グθ !
部帯電制御剤 ボントロンP−j/ 2
部上記配合とした以外はトナーA及び現像剤Aと同様な
方法でもつってトナーH及び現像剤Hを調整し、印字テ
ストした結果を第2表に示す。(Comparative Example 3) Resin Polyester resin A ioθ
Part coloring agent Mitsubishi carbon plastic, Rig θ!
Charge control agent Bontron P-j/2
Table 2 shows the results of a printing test using toner H and developer H prepared in the same manner as toner A and developer A except for the above formulation.
その結果、初期よシカブリが悪く、帯電量も経時的に低
レベルで推移し、画像も不良であったO
第7表
第7表(つソき)
第2表
○:良好。As a result, fogging was poor at the beginning, the amount of charge remained at a low level over time, and the image was poor.
Δ : やや良好。Δ: Somewhat good.
:不良 (発明の効果) 以上述べた様に、 本発明の正帯電性トナーを 用いることにより高品位の画質で、 しかも経時 的な性能劣化の少ない長寿命の現像剤が得られる。: Bad (Effect of the invention) As mentioned above, The positively chargeable toner of the present invention By using high-quality images, And over time A long-life developer with little deterioration in performance can be obtained.
三菱化成株式会社Mitsubishi Chemical Corporation
Claims (1)
るトナーにおいて、該荷電制御剤が少なくとも下記一般
式で表わせるトリアミノトリフエニルメタン系化合物を
樹脂100重量部に対して0.05〜10重量部含有せ
しめたことを特徴とする正荷電性トナー。 ▲数式、化学式、表等があります▼ (Rは炭素数1〜5のアルキル基を表わす。)(1) In a toner comprising at least a resin, a colorant, and a charge control agent, the charge control agent contains at least 0.05 to 10 parts by weight of a triaminotriphenylmethane compound represented by the following general formula per 100 parts by weight of the resin. 1. A positively charged toner characterized by containing: ▲There are mathematical formulas, chemical formulas, tables, etc.▼ (R represents an alkyl group having 1 to 5 carbon atoms.)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1089207A JP2946523B2 (en) | 1989-04-08 | 1989-04-08 | Two-component positively charged developer |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1089207A JP2946523B2 (en) | 1989-04-08 | 1989-04-08 | Two-component positively charged developer |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02267565A true JPH02267565A (en) | 1990-11-01 |
JP2946523B2 JP2946523B2 (en) | 1999-09-06 |
Family
ID=13964273
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1089207A Expired - Lifetime JP2946523B2 (en) | 1989-04-08 | 1989-04-08 | Two-component positively charged developer |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2946523B2 (en) |
-
1989
- 1989-04-08 JP JP1089207A patent/JP2946523B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JP2946523B2 (en) | 1999-09-06 |
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