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首页> 外文期刊>RSC Advances >Preparation of cis-pinane via α-pinene hydrogenation in water by using Ru nanoparticles immobilized in functionalized amphiphilic mesoporous silica
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Preparation of cis-pinane via α-pinene hydrogenation in water by using Ru nanoparticles immobilized in functionalized amphiphilic mesoporous silica

机译:用功能化两亲介孔二氧化硅固定化Ru纳米粒子通过水中的α-pine烯加氢制备顺式 -ane烷

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Amphiphilic mesoporous silica modified with trimethoxy (3,3,3-trifluoropropyl) silane (TFPS) and (3-aminopropyl) trimethoxysilane (APTS) was prepared by one-step synthesis. The structure and morphology of the mesoporous silica were characterized and confirmed by solid-state nuclear magnetic resonance, X-ray diffraction (XRD), N2 adsorption–desorption, Fourier transfer infrared spectroscopy (FT-IR), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Meanwhile, the thermostability of the amphiphilic mesoporous silica was detected by thermogravimetric (TG) technique. Highly dispersed Ru nanoparticles supported on such amphiphilic mesoporous silica (marked as Ru/MF@MN) were synthesized by wet impregnation method with the assistance of ultrasonic. The catalyst was characterized by X-ray photoelectron spectroscopy (XPS) and inductively coupled plasma-atomic emission spectrometry (ICP-AES). In water medium, Ru/MF@MN was used in α-pinene hydrogenation to prepare cis-pinane. Under the optimum reaction conditions (35 °C, 2 MPa H2, 1 h, m (H2O)?:?m (α-pinene)?:?m (Ru/MF@MN) = 200?:?60?:?1), 99.9% α-pinene conversion and 98.9% cis-pinane selectivity were obtained. When Ru/MF@MN was recycled six times, the conversion slightly decreased and the selectivity was nearly unchanged.
机译:通过一步合成,制备了用三甲氧基(3,3,3-三氟丙基)硅烷(TFPS)和(3-氨基丙基)三甲氧基硅烷(APTS)改性的两亲介孔二氧化硅。通过固态核磁共振,X射线衍射(XRD),N 2 吸附-解吸,傅里叶转移对介孔二氧化硅的结构和形貌进行了表征和确认。红外光谱(FT-IR),扫描电子显微镜(SEM)和透射电子显微镜(TEM)。同时,通过热重(TG)技术检测两亲介孔二氧化硅的热稳定性。在超声辅助下,通过湿法浸渍法合成了负载在两亲性介孔二氧化硅上的高分散Ru纳米颗粒(标记为Ru / MF @ MN)。通过X射线光电子能谱(XPS)和电感耦合等离子体原子发射光谱法(ICP-AES)对催化剂进行了表征。在水介质中,Ru / MF @ MN用于α-pine烯的加氢反应制备顺式em烷。在最佳反应条件下(35°C,2 MPa H 2 ,1 h, m (H 2 < / sub> O)?:? m (α-pine烯)?:? m (Ru / MF @ MN)= 200?:?60? :?1),获得99.9%的α-pine烯转化率和98.9%的顺式 pin烷选择性。当Ru / MF @ MN循环使用六次时,转化率略有下降,选择性几乎保持不变。

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