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
Catalytic hydrodeoxygenation of anisole as lignin model compound over supported nickel catalysts
点击次数:
论文类型:期刊论文
发表时间:2014-10-01
发表刊物:2nd International Congress on Catalysis for Biorefineries (CatBior)
收录刊物:SCIE、EI、CPCI-S、Scopus
卷号:234
期号:,SI
页面范围:125-132
ISSN号:0920-5861
关键字:Hydrodeoxygenation; Anisole; Methoxy group; Lignin; Supported-nickel catalysts
摘要:Catalytic hydrodeoxygenation (HDO) of anisole, a methoxy-rich lignin model compound, has been investigated over a series of Ni-containing (10 wt% loading) catalysts with activated carbon, SBA-15, SiO2, and gamma-Al2O3 supports, in order to understand their ability for removal of -OCH3 from anisole. This catalytic reaction had been carried out in an autoclave at 180-220 degrees C and 0.5-3.0 MPa H-2 pressure. Nickel-catalyzed aromatic ring-hydrogenation compared with the subsequent demethylation and deoxygenation is the fastest step in HDO of anisole under the present reaction conditions. Among these catalysts, the aromatic ring-saturated cyclohexyl methyl ether is mainly obtained over Ni/AC, while the Ni/SiO2 displayed the highest activity in HDO of anisole (selectivity to deoxygenated products >95%). Differences in HDO efficiency among the catalysts are attributed not only to variations in the dispersion of the active phase, but also to the acid sites which may contribute to the cleavage of C-O bonds. It has also been shown that the activity toward oxygen-removal strongly depended on reaction temperature and the conversion of anisole favors the production of oxygen-free aromatics by the direct demethoxylation pathway at the relatively low H-2 pressure. (C) 2014 Elsevier B.V. All rights reserved.