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
Hydrodeoxygenation of benzofuran over activated carbon supported Pt, Pd, and Pt-Pd catalysts
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论文类型:期刊论文
发表时间:2012-12-01
发表刊物:REACTION KINETICS MECHANISMS AND CATALYSIS
收录刊物:Scopus、SCIE、EI
卷号:107
期号:2
页面范围:393-404
ISSN号:1878-5190
关键字:Hydrodeoxygenation; Benzofuran; Reaction network; Palladium; Platinum
摘要:Activated carbon supported Pt, Pd, and Pt-Pd catalysts have been successfully prepared by incipient wet impregnation with a hydrochloric solution of PdCl2 and PtCl4. Hydrodeoxygenation of benzofuran was used as a probe reaction to investigate their catalytic properties. The activated carbon supported Pt-Pd catalyst was confirmed to form Pt-Pd alloy by X-ray diffraction. All the catalysts were active in the hydrodeoxygenation of benzofuran. Pd catalyst did not only give higher hydrogenation activity, but also showed faster deoxygenation rate than the Pt catalyst. The Pt-Pd catalyst with the mole ratio of Pd/Pt = 4 showed the highest catalytic activity among all of the catalysts. 2-Ethylcyclohexanone, which was not observed over the sulfide catalysts, was detected as a new oxygen-containing intermediate in the hydrodeoxygenation of benzofuran over the activated carbon supported Pt, Pd, and Pt-Pd catalysts. A ketone/enol isomerization reaction route is proposed to happen over the activated carbon supported noble metal Pt, Pd, and Pt-Pd catalysts.