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Title: Modeling lignin liquefaction: 1. Catalytic hydroprocessing of lignin-related methoxyphenols and interaromatic unit linkages

Journal Article · · Fuel Sci. Technol. Int.; (United States)

The reactions of two sets of lignin model compounds over a sulfided CoOMoO/sub 3//..gamma..-Al/sub 2/O/sub 3/ catalyst were studied. The first set mimicked lignin methoxyphenol residues and comprised 4-methyl-guaiacol, 4-methylcatechol, eugenol and vanillin. Deoxygenation and hydrogenation were facile and led to ultimate molar yields of single-ring products as high as 0.70. The selectivity to single-ring products increased with increases in temperature. o-hydroxydiphenylmethane, phenyl ether and o,o'-biphenol constituted the second set that mimicked thermally stable lignin bonds. Fragmentation of o-hydroxydiphenylmethane and phenyl ether occurred readily; o,o'-biphenol reacted to dibenzofuran.

Research Organization:
Dept. of Chemical Engineering, Univ. of Delaware, Newark, DE 19716
OSTI ID:
6509681
Journal Information:
Fuel Sci. Technol. Int.; (United States), Vol. 5:1
Country of Publication:
United States
Language:
English