JP2016113305A5 - - Google Patents

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Publication number
JP2016113305A5
JP2016113305A5 JP2014250355A JP2014250355A JP2016113305A5 JP 2016113305 A5 JP2016113305 A5 JP 2016113305A5 JP 2014250355 A JP2014250355 A JP 2014250355A JP 2014250355 A JP2014250355 A JP 2014250355A JP 2016113305 A5 JP2016113305 A5 JP 2016113305A5
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JP
Japan
Prior art keywords
silicone oil
hydrophobic silica
silica
amount
less
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JP2014250355A
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Japanese (ja)
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JP6393177B2 (en
JP2016113305A (en
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Priority claimed from JP2014250355A external-priority patent/JP6393177B2/en
Priority to JP2014250355A priority Critical patent/JP6393177B2/en
Priority to PCT/JP2015/084377 priority patent/WO2016093221A1/en
Priority to CN201580045419.1A priority patent/CN107074564B/en
Priority to MYPI2017700640A priority patent/MY176249A/en
Priority to KR1020177005448A priority patent/KR102422958B1/en
Publication of JP2016113305A publication Critical patent/JP2016113305A/en
Publication of JP2016113305A5 publication Critical patent/JP2016113305A5/ja
Publication of JP6393177B2 publication Critical patent/JP6393177B2/en
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Claims (9)

湿式法合成シリカをシリコーンオイルで表面処理した疎水性シリカであって、
前記疎水性シリカは、
(i)トルエンへのシリコーンオイル溶出量が、疎水性シリカ質量に対して0.2%未満である、但し、前記溶出量は、トルエンに2%の濃度で分散し、20℃で24時間経過後の分散前と対比したシリコーンオイル溶出率である、前記疎水性シリカ。
Hydrophobic silica obtained by surface treatment of wet synthetic silica with silicone oil,
The hydrophobic silica is
(i) The elution amount of silicone oil in toluene is less than 0.2% with respect to the mass of hydrophobic silica, provided that the elution amount is dispersed in toluene at a concentration of 2%, and after 24 hours at 20 ° C. The hydrophobic silica, which has a silicone oil elution rate compared with that before dispersion.
前記疎水性シリカは、ナトリウム成分の含有量がNa2O換算で0.20〜1.20 wt%であり、硫黄成分の含有量がSO3換算で0.25〜1.30 wt%である、請求項1に記載の疎水性シリカ。 The hydrophobic silica according to claim 1, wherein the hydrophobic silica has a sodium component content of 0.20 to 1.20 wt% in terms of Na 2 O and a sulfur component content of 0.25 to 1.30 wt% in terms of SO 3. Silica. シリコーンオイルの処理量が原料シリカのBET比表面積100 m2/gあたり3部〜9部であることを特徴とする請求項1又は2に記載の疎水性シリカ。 3. The hydrophobic silica according to claim 1, wherein the treatment amount of the silicone oil is 3 to 9 parts per 100 m 2 / g of BET specific surface area of the raw silica. (ii)M値が20%以上であり、及び/又は
(iii)DBA吸着量が100 m・mol/kg未満である、
請求項1又は2に記載の疎水性シリカ。
(ii) M value is 20% or more and / or
(iii) DBA adsorption amount is less than 100 m ・ mol / kg,
The hydrophobic silica according to claim 1 or 2.
湿式法合成シリカをシリコーンオイルで表面処理した疎水性シリカの製造方法であって、
強酸強塩基型中性塩化合物を存在させた湿式法合成シリカの表面にシリコーンオイルを被覆し、但し、湿式法合成シリカの表面における前記強酸強塩基型中性塩化合物の存在量が、0.3〜3.0%の範囲である、次いで、被覆したシリコーンオイルと湿式法合成シリカのシラノール基とがシロキサン結合を形成する条件に供して、疎水性シリカを得ることを含む、前記方法。
A process for producing hydrophobic silica obtained by surface treatment of a wet process synthetic silica with silicone oil,
Silicone oil is coated on the surface of the wet method synthetic silica in which the strong acid strong base type neutral salt compound is present, provided that the amount of the strong acid strong base type neutral salt compound on the surface of the wet method synthetic silica is 0. Said method comprising subjecting the coated silicone oil and the silanol groups of the wet-process synthetic silica to a siloxane bond in a range of 3 to 3.0% to obtain a hydrophobic silica.
前記強酸強塩基型中性塩化合物が硫酸ナトリウム、塩化ナトリウム、硫酸カリウム、塩化カリウムまたはそれらの混合物である請求項5に記載の製造方法。 The production method according to claim 5, wherein the strong acid strong base type neutral salt compound is sodium sulfate, sodium chloride, potassium sulfate, potassium chloride or a mixture thereof. 前記疎水性シリカは、トルエンへのシリコーンオイル溶出量が、疎水性シリカ質量に対して0.2%未満である、但し、前記溶出量は、トルエンに2%の濃度で分散し、20℃で24時間経過後の分散前と対比したシリコーンオイル溶出率である、請求項5〜のいずれかに記載の製造方法。 The hydrophobic silica has an elution amount of silicone oil in toluene of less than 0.2% based on the mass of the hydrophobic silica, provided that the elution amount is dispersed in toluene at a concentration of 2% and is heated at 20 ° C. for 24 hours. The production method according to any one of claims 5 to 6 , which is a silicone oil elution rate compared with that before dispersion after the lapse of time. 前記疎水性シリカは、
(i)M値が20%以上であり、及び/又は
(ii)DBA吸着量が100 m・mol/kg未満である、請求項5〜のいずれかに記載の製造方法。
The hydrophobic silica is
(i) M value is 20% or more and / or
(ii) The production method according to any one of claims 5 to 6 , wherein the DBA adsorption amount is less than 100 m · mol / kg.
前記シリコーンオイルが、動粘度が500センチストークス以下であるシリコーンオイルである請求項5〜のいずれかに記載の製造方法。
The silicone oil, the production method according to any one of claims 5-8 kinematic viscosity of silicone oil is 500 cSt or less.
JP2014250355A 2014-12-10 2014-12-10 Hydrophobic silica and method for producing the same Active JP6393177B2 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP2014250355A JP6393177B2 (en) 2014-12-10 2014-12-10 Hydrophobic silica and method for producing the same
KR1020177005448A KR102422958B1 (en) 2014-12-10 2015-12-08 Hydrophobic silica and method for producing same
CN201580045419.1A CN107074564B (en) 2014-12-10 2015-12-08 Hydrophobic silica and method for producing same
MYPI2017700640A MY176249A (en) 2014-12-10 2015-12-08 Hydrophobic silica and method for producing same
PCT/JP2015/084377 WO2016093221A1 (en) 2014-12-10 2015-12-08 Hydrophobic silica and method for producing same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2014250355A JP6393177B2 (en) 2014-12-10 2014-12-10 Hydrophobic silica and method for producing the same

Publications (3)

Publication Number Publication Date
JP2016113305A JP2016113305A (en) 2016-06-23
JP2016113305A5 true JP2016113305A5 (en) 2017-11-24
JP6393177B2 JP6393177B2 (en) 2018-09-19

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JP2014250355A Active JP6393177B2 (en) 2014-12-10 2014-12-10 Hydrophobic silica and method for producing the same

Country Status (5)

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JP (1) JP6393177B2 (en)
KR (1) KR102422958B1 (en)
CN (1) CN107074564B (en)
MY (1) MY176249A (en)
WO (1) WO2016093221A1 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2021527734A (en) * 2018-06-15 2021-10-14 ダブリュー・アール・グレース・アンド・カンパニー−コーンW R Grace & Co−Conn Defoaming agent Active substance, its manufacturing method, and defoaming compound
CN110202893A (en) * 2019-05-29 2019-09-06 安徽集友新材料股份有限公司 Dumb light transfer paper and preparation method thereof and dumb light shift extrusion coating paper
CN110204979A (en) * 2019-05-29 2019-09-06 安徽集友新材料股份有限公司 Dumb paint and preparation method thereof
KR102214188B1 (en) * 2020-12-24 2021-02-08 전순분 Opv composition for overprinting on packing film
KR102605531B1 (en) * 2021-11-02 2023-11-22 (재)울산테크노파크 Epoxy adhesive composition and manufacturing method thereof
CN116554943A (en) * 2023-03-29 2023-08-08 安徽沸点新材料有限公司 High-temperature-resistant silicone oil composite lubricating ester and preparation method thereof

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JPS54101795A (en) 1978-01-30 1979-08-10 Toyo Soda Mfg Co Ltd Hydrophobic rendering method for oxide fine powder
JPS58208124A (en) * 1982-05-28 1983-12-03 Nippon Shirika Kogyo Kk Hydrophobic precipitated silicic acid and its manufacture
JPH06316408A (en) * 1993-05-06 1994-11-15 Nippon Shirika Kogyo Kk Production of hydrophobic wet type synthetic silicic acid
JP3534464B2 (en) 1994-12-22 2004-06-07 東ソー・シリカ株式会社 Partially hydrophobized precipitated silica
JP4723080B2 (en) * 2000-11-28 2011-07-13 東レ・ダウコーニング株式会社 Anti-vibration silicone compound
EP1559744A1 (en) * 2004-01-30 2005-08-03 Rhodia Chimie Use of a pretreated precipitated silica as a reinforcing filler for silicone elastomer and curable compositions thus obtained
JP3997262B2 (en) * 2004-03-30 2007-10-24 サンノプコ株式会社 Antifoam
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