个人信息Personal Information
教授
博士生导师
硕士生导师
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. 能源化工. 物理化学
办公地点:西校区化工实验楼B525
电子邮箱:liganghg@dlut.edu.cn
In situ synthesis of Au/Ti-HMS and its catalytic performance in oxidation of bulky sulfur compounds using in situ generated H2O2 in the presence of H-2/O-2
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论文类型:期刊论文
发表时间:2009-04-15
发表刊物:MICROPOROUS AND MESOPOROUS MATERIALS
收录刊物:SCIE、EI
卷号:120
期号:3
页面范围:346-350
ISSN号:1387-1811
关键字:In situ; Gold; Mesoporous silicas; Direct synthesis; Oxidative desulphurization
摘要:Gold particles are supported on Ti-containing mesoporous silica (Ti-HMS) through an in situ process. The obtained samples were characterized by a series of techniques including ICP, powder X-ray diffraction, N-2 sorption, UV-visible spectroscopy and transmission electron microscopy. The performance of the catalyst in direct synthesis of H2O2 from H-2/O-2 in methanol solvent and oxidative desulphurization using the in situ generated H2O2 have been systematically investigated. The results show that in situ synthesized Au/Ti-HMS, the organic template of which is eliminated via extraction with ethanol, successfully maintains the typical wormhole structure of HMS and possesses uniform mesopores, which is confirmed by N-2 sorption and TEM. UV-visible spectroscopy result confirms the simultaneous existence of Au and Ti active centers in this bifunctional catalyst. Gold particles supported on Ti-HMS show high activity in the direct synthesis of H2O2 from H-2 and O-2 in methanol solvent. Furthermore, high removal rate of bulky sulfur compounds can be obtained using the in situ generated H2O2 over Au/Ti-HMS. Final conversion rate of the substrates confirms the dominant role of the in situ H2O2 oxidation in deep desulphurization. In addition, this bifunctional catalyst can avoid the insufficiency of H2O2 caused by the decomposition comparing with the Ti-HMS/commercial H2O2 system. Crown Copyright (C) 2008 Published by Elsevier Inc. All rights reserved.