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Indexed by:Journal Papers

Date of Publication:2014-10-01

Journal:2nd International Congress on Catalysis for Biorefineries (CatBior)

Included Journals:SCIE、EI、CPCI-S、Scopus

Volume:234

Issue:,SI

Page Number:125-132

ISSN No.:0920-5861

Key Words:Hydrodeoxygenation; Anisole; Methoxy group; Lignin; Supported-nickel catalysts

Abstract: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.