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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A non-alkoxide sol-gel route to highly active and selective Cu-Cr catalysts for glycerol conversion

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论文类型:期刊论文

发表时间:2010-01-01

发表刊物:JOURNAL OF MATERIALS CHEMISTRY

收录刊物:SCIE、EI

卷号:20

期号:4

页面范围:755-760

ISSN号:0959-9428

摘要:A non-alkoxide sol-gel route to highly active and selective Cu-Cr catalysts for glycerol conversion is presented. The addition of propylene oxide to ethanol solutions of Cr(NO(3))(3)center dot 9H(2)O and Cu(NO(3))(2)center dot 3H(2)O resulted in the formation of transparent Cu-Cr gels. The resulting gels were converted to the Cu-Cr catalysts by atmospheric drying and calcination. The Cu-Cr catalysts are characterized by X-ray diffraction (XRD), N(2) physisorption, temperature-programmed reduction (TPR), and transmission electron microscopy (TEM). The results show that the surface area of the Cu-Cr catalyst is adjusted by the hydrolysis conditions, Cu/Cr molar ratio, and treatment conditions (such as gas atmosphere and final temperature). For the sample with Cu/Cr = 0.5, the surface area of Cu-Cr xerogel can reach 94 m(2)/g and decreased to only 31 m(2)/g after calcination at 500 degrees C. The catalysts show significant catalytic activity and selectivity in glycerol conversion, i.e. above 52% conversion of glycerol and above 88% selectivity to 1,2-propanediol at 210 degrees C and 4.15 MPa H(2) pressure. CuCr(2)O(4) supported Cu catalysts are much more active than Cr(2)O(3) supported Cu catalysts. This indicates a strong interaction between Cu and CuCr(2)O(4) that is significantly improving the effectiveness of the catalyst for glycerol conversion.