个人信息Personal Information
教授
博士生导师
硕士生导师
主要任职:盘锦校区管委会副主任兼教学与科研工作部部长
性别:男
毕业院校:大连理工大学
学位:博士
所在单位:化工学院
学科:工业催化. 物理化学
办公地点:化工实验楼B427
联系方式:18641143913
电子邮箱:guoxw@dlut.edu.cn
Modification of small-crystal titanium silicalite-1 with organic bases: Recrystallization and catalytic properties in the hydroxylation of phenol
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论文类型:期刊论文
发表时间:2013-02-26
发表刊物:APPLIED CATALYSIS A-GENERAL
收录刊物:SCIE、EI
卷号:453
页面范围:272-279
ISSN号:0926-860X
关键字:Titanium silicalite-1; Organic base; Recrystallization; Hydroxylation of phenol; Modification
摘要:Small-crystal titanium silicalite-1 (TS-1) with a crystal size of about 600 nm x 400 nm x 250 nm, was treated with different organic bases, including ethylamine, diethylamine, tetramethyl ammonium hydroxide, tetrapropyl ammonium hydroxide and tetrabutyl ammonium hydroxide. The treated TS-1 was characterized by X-ray powder diffraction (XRD), Fourier-transform infrared spectrum (FTIR), ultraviolet-visible diffuse reflectance spectrum (UV-vis), X-ray photoelectron spectrum (XPS), n-hexane and cyclohexane physical adsorption, nitrogen physisorption, inductive coupled plasma emission (ICP), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Modification with different bases led to different molar ratios of Si/Ti on the external surface, according to the XPS data. The TEM images showed that many irregular hollows were generated during modification, due to the random dissolution of framework silicon and titanium. The dissolved amorphous silica and titania recrystallize on the external surface of the TS-1 crystals in the presence of template, and different axis-oriented recrystallization occurred for different templates. Tetrapropyl ammonium favored a-orientation and tetrabutyl ammonium favored b-orientation. Especially the modification with tetrapropyl ammonium hydroxide improved the catalytic properties of small-crystal TS-1 for the hydroxylation of phenol. The conversion of phenol reached 32.6% over small-crystal TS-1 modified with 0.06 mol/L tetrapropyl ammonium hydroxide for 72 h. (C) 2013 Elsevier B.V. All rights reserved.