熊光

个人信息Personal Information

副教授

博士生导师

硕士生导师

性别:男

毕业院校:中科院大连化学物理研究所

学位:博士

所在单位:化工学院

学科:工业催化

办公地点:西部校区化工实验楼B423

联系方式:gxiong@dlut.edu.cn

电子邮箱:gxiong@dlut.edu.cn

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Transformation of SiO2 in Titanium Silicalite-1/SiO2 extrudates during tetrapropylammonium hydroxide treatment and improvement of catalytic properties for propylene epoxidation

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论文类型:期刊论文

发表时间:2014-10-01

发表刊物:CHEMICAL ENGINEERING JOURNAL

收录刊物:SCIE、EI、Scopus

卷号:253

页面范围:464-471

ISSN号:1385-8947

关键字:TS-1; TS-1/SiO2 extrudate; Transformation; TPAOH treatment; Propylene epoxidation

摘要:Titanium Silicalite-1 (TS-1)/SiO2 extrudates were treated with tetrapropylammonium hydroxide (TPAOH) solutions under hydrothermal conditions. The catalysts were characterized using various analysis techniques including X-ray diffraction (XRD), ultraviolet-visible diffuse reflectance spectroscopy (UV-Vis), UV Raman, X-ray photoelectron spectroscopy (XPS), nitrogen physisorption, X-ray fluorescence (XRF), Si-29 magic-angle-spinning nuclear magnetic resonance (Si-29 MAS NMR) spectroscopy, and transmission electron microscopy (TEM). The transformation of amorphous SiO2 in TS-1/SiO2 catalysts during TPAOH treatment was studied in detail. The results show that the SiO2 dissolved and then crystallized during TPAOH treatment, which increased the hydrophobicity and the ratio of Si/Ti on the external surface of TS-1. Moreover, the existence of SiO2 inhibited the formation of anatase TiO2 during TPAOH treatment. The changes in physical and chemical properties not only improved the catalytic activity but also improved the stability of catalysts after TPAOH treatment. The experimental results show that the treated TS-1/SiO2 catalysts exhibited higher catalytic activity and stability than the untreated counterparts. Especially for the TS-1/SiO2 catalyst treated with 0.06 mol/L TPAOH solution for 72 h, the H2O2 conversion still remained above 90% and the propylene oxide selectivity was as high as 99% after a long-term run with time on stream (TOS) of 648 h. (C) 2014 Elsevier B.V. All rights reserved.