JP2019032492A5 - - Google Patents

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JP2019032492A5
JP2019032492A5 JP2017154827A JP2017154827A JP2019032492A5 JP 2019032492 A5 JP2019032492 A5 JP 2019032492A5 JP 2017154827 A JP2017154827 A JP 2017154827A JP 2017154827 A JP2017154827 A JP 2017154827A JP 2019032492 A5 JP2019032492 A5 JP 2019032492A5
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binder resin
crystalline compound
toner
fine particles
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JP2017154827A
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JP6910884B2 (en
JP2019032492A (en
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そこで本発明の一態様によれば、着色剤、結着樹脂、及び低分子結晶性化合物を含有するトナーであって、
該低分子結晶性化合物が、炭素数12〜26の長鎖炭化水素骨格と芳香族炭化水素骨格とを含むエーテル化合物であり、
該結着樹脂のSP値(SP1)と該低分子結晶性化合物のSP値(SP2)とが下記式を満足するトナーが提供される。
0(cal/mol)≦|SP1−SP2|≦3(cal/mol)
Therefore, according to one aspect of the present invention, the toner contains a colorant, a binder resin, and a low molecular weight crystalline compound.
The low molecular weight crystalline compound is an ether compound containing a long-chain hydrocarbon skeleton having 12 to 26 carbon atoms and an aromatic hydrocarbon skeleton.
Toner having an SP value of the binder resin (SP1) and the SP value of the low-molecular crystalline compound (SP2) and satisfies the following formulas are provided.
0 (cal / mol) ≤ | SP1-SP2 | ≤3 (cal / mol)

また、本発明の他の態様によれば、
結着樹脂の微粒子を分散した結着樹脂微粒子分散液、及び着色剤の微粒子を分散した着色剤微粒子分散液を混合し、結着樹脂微粒子、及び着色剤微粒子を凝集させて、コア凝集粒子を形成する工程、
該結着樹脂及び低分子結晶性化合物を有機溶媒に溶解させ、得られた溶解液を水系媒体に分散させる工程
該水系媒体中にて、該溶解液から該有機溶媒を除去して該結着樹脂及び該低分子結晶性化合物を含有する複合微粒子を得る工程、
該水系媒体中にて、該複合微粒子を該コア凝集粒子に付着させコアシェル粒子を形成する付着工程、及び
該コアシェル粒子を該結着樹脂のガラス転移温度以上の温度に加熱して融合させる融合工程、
を有するトナーの製造方法であって
該低分子結晶性化合物が、炭素数12〜26の長鎖炭化水素骨格と芳香族炭化水素骨格とを含むエーテル化合物であり、
該結着樹脂のSP値(SP1)と該低分子結晶性化合物のSP値(SP2)とが下記式を満足するトナーの製造方法が提供される。
0(cal/mol)≦|SP1−SP2|≦3(cal/mol)
Further, according to another aspect of the present invention.
The binder resin fine particle dispersion liquid in which the fine particles of the binder resin are dispersed and the colorant fine particle dispersion liquid in which the fine particles of the colorant are dispersed are mixed, and the binder resin fine particles and the colorant fine particles are agglomerated to form core agglomerated particles. The process of forming,
The binder resin and low-molecular crystalline compound is dissolved in an organic solvent, the resulting solution Ru is dispersed in an aqueous medium process,
C. in aqueous medium, and removing the organic solvent from the lysis solution, to obtain a composite fine particles containing the binder resin and the low molecular crystalline compound process,
An adhesion step of adhering the composite fine particles to the core agglomerated particles to form core-shell particles in the aqueous medium , and a fusion step of heating the core-shell particles to a temperature equal to or higher than the glass transition temperature of the binder resin to fuse them. ,
A method of manufacturing a toner have a,
The low molecular weight crystalline compound is an ether compound containing a long-chain hydrocarbon skeleton having 12 to 26 carbon atoms and an aromatic hydrocarbon skeleton.
Method for producing a toner having an SP value of the binder resin (SP1) and the SP value of the low-molecular crystalline compound (SP2) and satisfies the following formulas are provided.
0 (cal / mol) ≤ | SP1-SP2 | ≤3 (cal / mol)

Claims (5)

着色剤、結着樹脂、及び低分子結晶性化合物を含有するトナーであって、
該低分子結晶性化合物が、炭素数12〜26の長鎖炭化水素骨格と芳香族炭化水素骨格とを含むエーテル化合物であり、
該結着樹脂のSP値(SP1)と該低分子結晶性化合物のSP値(SP2)とが下記式を満足することを特徴とするトナー。
0(cal/mol)≦|SP1−SP2|≦3(cal/mol)
A toner containing a colorant, a binder resin, and a low molecular weight crystalline compound.
The low molecular weight crystalline compound is an ether compound containing a long-chain hydrocarbon skeleton having 12 to 26 carbon atoms and an aromatic hydrocarbon skeleton.
Toner having an SP value of the binder resin (SP1) and the SP value of the low-molecular crystalline compound (SP2) and is characterized by satisfying the following expression.
0 (cal / mol) ≤ | SP1-SP2 | ≤3 (cal / mol)
前記低分子結晶性化合物の融点が、50℃以上100℃以下である請求項1に記載のトナー。 The toner according to claim 1, wherein the low molecular weight crystalline compound has a melting point of 50 ° C. or higher and 100 ° C. or lower. 前記結着樹脂が、ビスフェノールAのプロピレンオキサイド付加物を50モル%以上含むアルコール成分とカルボン酸成分と縮重合体である非晶性ポリエステルである請求項1又は2に記載のトナー。 The binder resin, toner according to claim 1 or 2 is an amorphous polyester is a condensation polymer of an alcohol component and a carboxylic acid component comprising propylene oxide adduct of bisphenol A 50 mol% or more. 前記トナーが、前記結着樹脂、及び前記着色剤を含有するコアの表面に、前記結着樹脂、及び前記低分子結晶性化合物を含有するシェルを有するコアシェル構造のトナーである請求項1〜3のいずれか一項に記載のトナー。 Claims 1 to 3 are toners having a core-shell structure, wherein the toner has a shell containing the binder resin and the low molecular weight crystalline compound on the surface of a core containing the binder resin and the colorant. The toner according to any one of the above. 結着樹脂の微粒子を分散した結着樹脂微粒子分散液、及び着色剤の微粒子を分散した着色剤微粒子分散液を混合し、結着樹脂微粒子、及び着色剤微粒子を凝集させて、コア凝集粒子を形成する工程、
該結着樹脂及び低分子結晶性化合物を有機溶媒に溶解させ、得られた溶解液を水系媒体に分散させる工程
該水系媒体中にて、該溶解液から該有機溶媒を除去して該結着樹脂及び該低分子結晶性化合物を含有する複合微粒子を得る工程、
該水系媒体中にて、該複合微粒子を該コア凝集粒子に付着させコアシェル粒子を形成する付着工程、及び
該コアシェル粒子を該結着樹脂のガラス転移温度以上の温度に加熱して融合させる融合工程、
を有するトナーの製造方法であって
該低分子結晶性化合物が、炭素数12〜26の長鎖炭化水素骨格と芳香族炭化水素骨格とを含むエーテル化合物であり、
該結着樹脂のSP値(SP1)と該低分子結晶性化合物のSP値(SP2)とが下記式を満足することを特徴とするトナーの製造方法。
0(cal/mol)≦|SP1−SP2|≦3(cal/mol)
The binder resin fine particle dispersion liquid in which the fine particles of the binder resin are dispersed and the colorant fine particle dispersion liquid in which the fine particles of the colorant are dispersed are mixed, and the binder resin fine particles and the colorant fine particles are agglomerated to form core agglomerated particles. The process of forming,
The binder resin and low-molecular crystalline compound is dissolved in an organic solvent, the resulting solution Ru is dispersed in an aqueous medium process,
C. in aqueous medium, and removing the organic solvent from the lysis solution, to obtain a composite fine particles containing the binder resin and the low molecular crystalline compound process,
An adhesion step of adhering the composite fine particles to the core agglomerated particles to form core-shell particles in the aqueous medium , and a fusion step of heating the core-shell particles to a temperature equal to or higher than the glass transition temperature of the binder resin to fuse them. ,
A method of manufacturing a toner have a,
The low molecular weight crystalline compound is an ether compound containing a long-chain hydrocarbon skeleton having 12 to 26 carbon atoms and an aromatic hydrocarbon skeleton.
Method for producing a toner, wherein the SP value of the binder resin (SP1) and the SP value of the low-molecular crystalline compound (SP2) and satisfies the following expression.
0 (cal / mol) ≤ | SP1-SP2 | ≤3 (cal / mol)
JP2017154827A 2017-08-09 2017-08-09 Toner and toner manufacturing method Active JP6910884B2 (en)

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JP2019032492A JP2019032492A (en) 2019-02-28
JP2019032492A5 true JP2019032492A5 (en) 2020-09-24
JP6910884B2 JP6910884B2 (en) 2021-07-28

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Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6162045A (en) * 1984-09-03 1986-03-29 Konishiroku Photo Ind Co Ltd Toner for developing electrostatic charge image
EP0471894B1 (en) * 1990-08-22 1995-11-02 Agfa-Gevaert N.V. Particulate toner material
JPH10307418A (en) * 1997-05-07 1998-11-17 Fuji Xerox Co Ltd Production of electrostatic latent image developing toner, electrostatic latent image developing toner, electrostatic latent image developer and image forming method
US6037090A (en) * 1997-07-03 2000-03-14 Fuji Xerox Co., Ltd. Toner for electrophotography and method of preparation thereof
JP2010139903A (en) * 2008-12-15 2010-06-24 Konica Minolta Business Technologies Inc Method for producing toner, and toner
JP2010144008A (en) * 2008-12-17 2010-07-01 Fuji Xerox Co Ltd Resin composition, toner for electrophotography, developer for electrophotography, toner cartridge, process cartridge and image forming apparatus
US20100330486A1 (en) * 2009-06-24 2010-12-30 Xerox Corporation Toner Compositions
JP2013068910A (en) * 2011-09-26 2013-04-18 Fuji Xerox Co Ltd Toner for electrostatic charge image development, electrostatic charge image developer, toner cartridge, process cartridge, image forming apparatus, image forming method, and novel crystalline polyether for toner for electrostatic charge image development
US9069272B2 (en) * 2013-11-11 2015-06-30 Xerox Corporation Super low melt toner having small molecule plasticizers
US9188891B2 (en) * 2013-11-11 2015-11-17 Xerox Corporation Super low melt toner having crystalline aromatic ethers
JP6492860B2 (en) * 2015-03-26 2019-04-03 富士ゼロックス株式会社 Electrostatic image developing toner, electrostatic image developer, toner cartridge, process cartridge, image forming apparatus, and image forming method

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