梁长海

个人信息Personal Information

教授

博士生导师

硕士生导师

任职 : 大连理工大学成都研究院院长

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:化学工艺. 物理化学. 功能材料化学与化工

办公地点:大连理工大学西部校区化工综合楼A401室

联系方式:辽宁省大连市高新区凌工路2号,邮编116024

电子邮箱:changhai@dlut.edu.cn

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Effects of Synthetic Parameters on the Structure and Catalytic Performance of Cu-Cr Catalysts Prepared by a Non-Alkoxide Sol-Gel Route

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论文类型:期刊论文

发表时间:2011-02-16

发表刊物:INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH

收录刊物:Scopus、SCIE、EI

卷号:50

期号:4

页面范围:2031-2039

ISSN号:0888-5885

摘要:The surface areas of Cu-Cr xerogels prepared by an epoxide assisted route are highly dependent on synthetic conditions like gelation temperature, amount of water in the solvent, and gel aging time. Gelation temperature affects the relative rates of hydrolysis and condensation, the amount of water in solution adjusts the solution pH, and the aging process influences the microstructural properties of the xerogels. These factors affect the stability of the sol particles in solution and the final structure of the gel. Thermogravimetric and differential thermogravimetric analysis, specific surface area measurement through nitrogen adsorption, X-ray diffraction, scanning electron microscopy, and transmission electron microscopy are employed to determine particle size distribution and morphology of the different particulate products (i.e., gels, powders) obtained via different synthesis conditions, both before and after thermal treatments. The xerogel surface area can reach up to 230 m(2)/g by adjusting the operating parameters. Moreover, the results show that the Cu-Cr catalysts with CdCr(2)O(4) and Cr(2)O(3) phases obtained by calcining the as-prepared xerogels in 20% O(2) in Ar have better activity for glycerol catalytic conversion than catalysts with Cu and Cr(2)O(3) phases that were obtained by calcination in Ar. In addition, the activity of catalysts increased with the surface areas of xerogels. It is noteworthy that the catalysts have significant selectivity to 1,2-propanediol (54%) and 1-propanol (36%) at 32% conversion of glycerol at 210 degrees C and 4.1 MPa H(2) pressure.