JP5194322B2 - 環状フェノール硫化物の金属化合物を用いた電荷制御剤及びトナー - Google Patents
環状フェノール硫化物の金属化合物を用いた電荷制御剤及びトナー Download PDFInfo
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- JP5194322B2 JP5194322B2 JP2010511083A JP2010511083A JP5194322B2 JP 5194322 B2 JP5194322 B2 JP 5194322B2 JP 2010511083 A JP2010511083 A JP 2010511083A JP 2010511083 A JP2010511083 A JP 2010511083A JP 5194322 B2 JP5194322 B2 JP 5194322B2
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- toner
- acid
- phenol sulfide
- cyclic phenol
- metal compound
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- 125000005504 styryl group Chemical group 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
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- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 230000035900 sweating Effects 0.000 description 1
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- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- SJMYWORNLPSJQO-UHFFFAOYSA-N tert-butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(C)(C)C SJMYWORNLPSJQO-UHFFFAOYSA-N 0.000 description 1
- PFBLRDXPNUJYJM-UHFFFAOYSA-N tert-butyl 2-methylpropaneperoxoate Chemical compound CC(C)C(=O)OOC(C)(C)C PFBLRDXPNUJYJM-UHFFFAOYSA-N 0.000 description 1
- JIYXDFNAPHIAFH-UHFFFAOYSA-N tert-butyl 3-tert-butylperoxycarbonylbenzoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC(C(=O)OC(C)(C)C)=C1 JIYXDFNAPHIAFH-UHFFFAOYSA-N 0.000 description 1
- JZFHXRUVMKEOFG-UHFFFAOYSA-N tert-butyl dodecaneperoxoate Chemical compound CCCCCCCCCCCC(=O)OOC(C)(C)C JZFHXRUVMKEOFG-UHFFFAOYSA-N 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical class S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-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
- 238000004448 titration Methods 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical group 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 229910000391 tricalcium phosphate Inorganic materials 0.000 description 1
- 229940078499 tricalcium phosphate Drugs 0.000 description 1
- 235000019731 tricalcium phosphate Nutrition 0.000 description 1
- CAPIMQICDAJXSB-UHFFFAOYSA-N trichloro(1-chloroethyl)silane Chemical compound CC(Cl)[Si](Cl)(Cl)Cl CAPIMQICDAJXSB-UHFFFAOYSA-N 0.000 description 1
- FLPXNJHYVOVLSD-UHFFFAOYSA-N trichloro(2-chloroethyl)silane Chemical compound ClCC[Si](Cl)(Cl)Cl FLPXNJHYVOVLSD-UHFFFAOYSA-N 0.000 description 1
- CPUDPFPXCZDNGI-UHFFFAOYSA-N triethoxy(methyl)silane Chemical compound CCO[Si](C)(OCC)OCC CPUDPFPXCZDNGI-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- XYJRNCYWTVGEEG-UHFFFAOYSA-N trimethoxy(2-methylpropyl)silane Chemical compound CO[Si](OC)(OC)CC(C)C XYJRNCYWTVGEEG-UHFFFAOYSA-N 0.000 description 1
- ZNOCGWVLWPVKAO-UHFFFAOYSA-N trimethoxy(phenyl)silane Chemical compound CO[Si](OC)(OC)C1=CC=CC=C1 ZNOCGWVLWPVKAO-UHFFFAOYSA-N 0.000 description 1
- KHOQXNHADJBILQ-UHFFFAOYSA-N trimethyl(sulfanyl)silane Chemical compound C[Si](C)(C)S KHOQXNHADJBILQ-UHFFFAOYSA-N 0.000 description 1
- 239000005051 trimethylchlorosilane Substances 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- 229940096522 trimethylolpropane triacrylate Drugs 0.000 description 1
- PQDJYEQOELDLCP-UHFFFAOYSA-N trimethylsilane Chemical compound C[SiH](C)C PQDJYEQOELDLCP-UHFFFAOYSA-N 0.000 description 1
- GRPURDFRFHUDSP-UHFFFAOYSA-N tris(prop-2-enyl) benzene-1,2,4-tricarboxylate Chemical compound C=CCOC(=O)C1=CC=C(C(=O)OCC=C)C(C(=O)OCC=C)=C1 GRPURDFRFHUDSP-UHFFFAOYSA-N 0.000 description 1
- UJMBCXLDXJUMFB-UHFFFAOYSA-K trisodium;5-oxo-1-(4-sulfonatophenyl)-4-[(4-sulfonatophenyl)diazenyl]-4h-pyrazole-3-carboxylate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)C1=NN(C=2C=CC(=CC=2)S([O-])(=O)=O)C(=O)C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 UJMBCXLDXJUMFB-UHFFFAOYSA-K 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 235000019871 vegetable fat Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- JEVGKYBUANQAKG-UHFFFAOYSA-N victoria blue R Chemical compound [Cl-].C12=CC=CC=C2C(=[NH+]CC)C=CC1=C(C=1C=CC(=CC=1)N(C)C)C1=CC=C(N(C)C)C=C1 JEVGKYBUANQAKG-UHFFFAOYSA-N 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000001018 xanthene dye Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000001060 yellow colorant Substances 0.000 description 1
- 239000001052 yellow pigment Substances 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 1
- 229910000165 zinc phosphate Inorganic materials 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/097—Plasticisers; Charge controlling agents
- G03G9/09783—Organo-metallic compounds
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/097—Plasticisers; Charge controlling agents
- G03G9/09733—Organic compounds
- G03G9/0975—Organic compounds anionic
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/097—Plasticisers; Charge controlling agents
- G03G9/09733—Organic compounds
- G03G9/09775—Organic compounds containing atoms other than carbon, hydrogen or oxygen
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Developing Agents For Electrophotography (AREA)
Description
本発明は、また、該電荷制御剤を使用する高い帯電性能を有する新規な負帯電性トナーを提供することを目的とする。
本発明の環状フェノール硫化物の金属化合物を含有したトナーは、高湿あるいは低湿環境下においても帯電特性の変動が少なく、安定した現像特性を保持できる。
また、上記一般式(1)においてmが4ないし9の整数である環状フェノール硫化物の金属化合物を単独で用いても、2種以上混合して用いても良い。
本発明では、一般式(1)のYが水素である重合体1モルあたり、金属が約1モル反応するように、該金属化合物(金属付与剤)を反応させて調製するのが好ましい。特に、複数のYが金属原子と水素原子の組み合わせになっているのが好ましい。
本発明において、結着樹脂の分子量分布は、THFを溶媒としたGPCによって測定される。
また、ポリエステル系重合体、ビニル重合体とその他の結着樹脂を併用する場合、全体の結着樹脂の酸価が0.1〜50mgKOH/gを有する樹脂を60質量%以上有するものが好ましい。
(1)試料は予め結着樹脂(重合体成分)以外の添加物を除去して使用するか、結着樹脂および架橋された結着樹脂以外の成分の酸価および含有量を予め求めておく。試料の粉砕品0.5〜2.0gを精秤し、重合体成分の重さをWgとする。例えば、トナーから結着樹脂の酸価を測定する場合は、着色剤または磁性体などの酸価および含有量を別途測定しておき、計算により結着樹脂の酸価を求める。
(2)300(ml)のビーカーに試料を入れ、トルエン/エタノール(体積比4/1)の混合液150(ml)を加え溶解する。
(3)0.1mol/LのKOHのエタノール溶液を用いて、電位差滴定装置を用いて滴定する。
(4)この時のKOH溶液の使用量をS(ml)とし、同時にブランクを測定し、この時のKOH溶液の使用量をB(ml)とし、以下の式(1)で算出する。ただしfはKOH濃度のファクターである。
酸価(mgKOH/g)=[(S−B)×f×5.61]/W (1)
前記顔料を単独で使用しても構わないが、染料と顔料と併用してその鮮明度を向上させた方がフルカラー画像の画質の点からより好ましい。
フタロシアニン染料の代表例としてはC.I.ソルベントブルー25、55、70、C.I.ダイレクトブルー25、86、アルカリブルーレーキ、ビクトリアブルーレーキなどがあげられる。
前記の着色剤の使用量は結着樹脂100量部に対して、0.1〜20質量部が好ましい。
樹脂コートキャリアにおいて、キャリアコアの表面を少なくとも樹脂被覆剤で被覆する方法としては、樹脂を溶剤中に溶解若しくは懸濁せしめて塗布したキャリアコアに付着せしめる方法、あるいは単に粉体状態で混合する方法が適用できる。樹脂コートキャリアに対して樹脂被覆材の割合は、適宜決定すればよいが、樹脂コートキャリアに対し好ましくは0.01〜5質量%、より好ましくは0.1〜1質量%がよい。
可塑化作用を有するワックスの種類としては、例えば融点の低いワックス、または分子の構造上に分岐のあるものや極性基を有する構造のものであり、離型作用を有するワックスとしては、融点の高いワックス、分子の構造では、直鎖構造のものや、官能基を有さない無極性のものがあげられる。使用例としては、2種以上の異なるワックスの融点の差が10℃〜100℃のものの組み合わせや、ポリオレフィンとグラフト変性ポリオレフィンの組み合わせなどがあげられる。
本発明のトナーは、粉砕型トナーの場合の形状係数(SF−1)の平均値が100〜400が好ましく、形状係数2(SF−2)の平均値が100〜350が好ましい。
SF−1=((ML2×π)/4A)×100
(式中、MLは粒子の最大長、Aは一粒子の投影面積を示す。)
SF−2=(PM2/4Aπ)×100
(式中、PMは粒子の周囲長、Aは一粒子の投影面積を示す。)。
本発明のトナーのDSC測定において観測される吸熱ピークにおいて70〜120℃の領域に最大ピークのピークトップ温度があることが好ましい。
HPLCによる分析の結果、前記粗製物は一般式(1)においてRがtert−ブチルであり、mが4であり、nが0であり、Yの全てが水素原子である環状4量体がピーク面積比96.1%、一般式(1)においてRがtert−ブチルであり、mが8であり、nが0であり、Yの全てが水素原子である環状8量体がピーク面積比3.6%を示す混合物であることが分かった。
HPLCによる分析の結果、一般式(1)においてRがtert−ブチルであり、mが4であり、nが2であり、Yの全てが水素原子である酸化型の環状4量体がピーク面積比99.3%であった。
比較のために、実施例1で合成した環状フェノール硫化物の亜鉛化合物を、実施例1で得られた前記した環状4量体(一般式(1)においてRがtert−ブチルであり、mが4であり、nが0であり、Yの全てが水素原子である環状4量体)に代えて、実施例5と同様の方法でトナーを作製した後、時定数、飽和帯電量を測定した。結果は表1にまとめて示した。
[比較例B]
比較のために、実施例1で合成した環状フェノール硫化物の亜鉛化合物を、実施例3で得られた前記した酸化型の環状4量体(一般式(1)においてRがtert−ブチルであり、mが4であり、nが2であり、Yの全てが水素原子である酸化型の環状4量体)に代えて、実施例5と同様の方法でトナーを作製した後、時定数、飽和帯電量を測定した。結果は表1にまとめて示した。
比較のために、実施例1で合成した環状フェノール硫化物の亜鉛化合物を、サリチル酸の亜鉛錯体に代えて、実施例5と同様の方法でトナーを作製した後、時定数、飽和帯電量を測定した。結果は表1にまとめて示した。
比較のために、実施例1で合成した環状フェノール硫化物の亜鉛化合物を、サリチル酸のアルミニウム錯体に代えて、実施例5と同様の方法でトナーを作製した後、時定数、飽和帯電量を測定した。結果は表1にまとめて示した。
比較のために、実施例1で合成した環状フェノール硫化物の亜鉛化合物を、カリックスアレーンに代えて、実施例5と同様の方法でトナーを作製した後、時定数、飽和帯電量を測定した。結果は表1にまとめて示した。
比較のために、実施例1で合成した環状フェノール硫化物の亜鉛化合物を、実施例1で得られた前記した環状4量体(一般式(1)においてRがtert−ブチルであり、mが4であり、nが0であり、Yの全てが水素原子である環状4量体)に代えて、実施例9と同様の方法でトナーを作製した後、時定数、飽和帯電量を測定した。結果は表1にまとめて示した。
[比較例D]
比較のために、実施例1で合成した環状フェノール硫化物の亜鉛化合物を、実施例3で得られた前記した酸化型の環状4量体(一般式(1)においてRがtert−ブチルであり、mが4であり、nが2であり、Yの全てが水素原子である酸化型の環状4量体)に代えて、実施例9と同様の方法でトナーを作製した後、時定数、飽和帯電量を測定した。結果は表1にまとめて示した。
比較のために、実施例1で合成した環状フェノール硫化物の亜鉛化合物を、サリチル酸の亜鉛錯体に代えて、実施例9と同様の方法でトナーを作製した後、時定数、飽和帯電量を測定した。結果は表1にまとめて示した。
比較のために、実施例1で合成した環状フェノール硫化物の亜鉛化合物を、サリチル酸のアルミニウム錯体に代えて、実施例9と同様の方法でトナーを作製した後、時定数、飽和帯電量を測定した。
結果は表1にまとめて示した。
比較のために、実施例1で合成した環状フェノール硫化物の亜鉛化合物を、カリックスアレーンに代えて、実施例9と同様の方法でトナーを作製した後、時定数、飽和帯電量を測定した。
結果は表1にまとめて示した。
特に、表1に示した比較例A、B、C及びD(これらはいずれも式中のYが全て水素原子である化合物を用いたもの)と実施例5、7、9及び11(これらはいずれも式中のYの一部が金属原子となっている化合物を用いたもの)の性能をそれぞれ比較すると、Yの一部を金属原子とすることによって、飽和帯電量が大きくなり、かつ時定数は小さくなっており(時定数が小さいほど帯電の立ち上がりが良好)、本発明の電荷制御剤は、近年のプリンターの高速化に一層適したものであることがわかる。
Claims (12)
- 一般式(1)で表される環状フェノール硫化物の金属化合物であって、mが4である請求項1記載の電荷制御剤。
- 一般式(1)で表される環状フェノール硫化物の金属化合物であって、mが6である請求項1記載の電荷制御剤。
- 一般式(1)で表される環状フェノール硫化物の金属化合物であって、mが8である請求項1記載の電荷制御剤。
- 一般式(1)で表される環状フェノール硫化物の金属化合物であって、nが0である請求項2ないし4のいずれか1項記載の電荷制御剤。
- 一般式(1)で表される環状フェノール硫化物の金属化合物であって、nが2である請求項2ないし4のいずれか1項記載の電荷制御剤。
- 請求項1記載の一般式(1)で表される環状フェノール硫化物の金属化合物の1種以上と着色剤および結着樹脂を含有することを特徴とするトナー。
- 請求項1記載の一般式(1)で表される環状フェノール硫化物の金属化合物であって、mが4である環状フェノール硫化物の金属化合物の1種以上と着色剤および結着樹脂を含有することを特徴とするトナー。
- 請求項1記載の一般式(1)で表される環状フェノール硫化物の金属化合物であって、mが6である環状フェノール硫化物の金属化合物の1種以上と着色剤および結着樹脂を含有することを特徴とするトナー。
- 請求項1記載の一般式(1)で表される環状フェノール硫化物の金属化合物であって、mが8である環状フェノール硫化物の金属化合物の1種以上と着色剤および結着樹脂を含有することを特徴とするトナー。
- 請求項1記載の一般式(1)で表される環状フェノール硫化物の金属化合物であって、nが0である環状フェノール硫化物の金属化合物の1種以上と着色剤および結着樹脂を含有することを特徴とするトナー。
- 請求項1記載の一般式(1)で表される環状フェノール硫化物の金属化合物であって、nが2である環状フェノール硫化物の金属化合物の1種以上と着色剤および結着樹脂を含有することを特徴とするトナー。
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PCT/JP2009/058677 WO2009136634A1 (ja) | 2008-05-09 | 2009-05-08 | 環状フェノール硫化物の金属化合物を用いた電荷制御剤及びトナー |
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WO2007111346A1 (ja) * | 2006-03-29 | 2007-10-04 | Hodogaya Chemical Co., Ltd. | 混合環状フェノール硫化物、それを用いた電荷制御剤及びトナー |
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JP3534534B2 (ja) * | 1996-04-11 | 2004-06-07 | オリヱント化学工業株式会社 | 静電荷像現像用トナー |
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- 2009-05-08 WO PCT/JP2009/058677 patent/WO2009136634A1/ja active Application Filing
- 2009-05-08 KR KR1020107027144A patent/KR20110003570A/ko not_active Application Discontinuation
- 2009-05-08 JP JP2010511083A patent/JP5194322B2/ja not_active Expired - Fee Related
- 2009-05-08 EP EP09742758.7A patent/EP2287674B1/en not_active Not-in-force
- 2009-05-08 US US12/990,484 patent/US20110045396A1/en not_active Abandoned
- 2009-05-08 CN CN200980126718.2A patent/CN102089717B/zh not_active Expired - Fee Related
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JPH1149770A (ja) * | 1997-08-08 | 1999-02-23 | Cosmo Sogo Kenkyusho:Kk | 環状フェノール硫化物の製造法 |
JP2000273096A (ja) * | 1999-03-19 | 2000-10-03 | Cosmo Research Inst | 環状フェノール硫化物の製造方法 |
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EP2287674A1 (en) | 2011-02-23 |
CN102089717B (zh) | 2013-11-06 |
EP2287674B1 (en) | 2014-03-05 |
JPWO2009136634A1 (ja) | 2011-09-08 |
US20110045396A1 (en) | 2011-02-24 |
EP2287674A4 (en) | 2012-04-25 |
KR20110003570A (ko) | 2011-01-12 |
CN102089717A (zh) | 2011-06-08 |
WO2009136634A1 (ja) | 2009-11-12 |
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