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Highly Selective Hydrodecarbonylation of Oleic Acid into n ‐Heptadecane over a Supported Nickel/Zinc Oxide–Alumina Catalyst
Author(s) -
Li Guangci,
Zhang Feng,
Chen Lei,
Zhang Chuanhui,
Huang He,
Li Xuebing
Publication year - 2015
Publication title -
chemcatchem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.497
H-Index - 106
eISSN - 1867-3899
pISSN - 1867-3880
DOI - 10.1002/cctc.201500418
Subject(s) - heptadecane , deoxygenation , oleic acid , chemistry , catalysis , stearic acid , hydrodeoxygenation , inorganic chemistry , selectivity , dehydrogenation , decarbonylation , organic chemistry , biochemistry
The production of second‐generation biodiesel with triglycerides or their derivatives through hydroprocessing is considered as a promising approach to make transportation fuels. In this study, a series of Ni‐based catalysts supported on basic composite oxides (MO‐Al 2 O 3 , M=Mg, Ca, Ni, Cu, Zn) were prepared for the catalytic deoxygenation of oleic acid in the presence of H 2 . Ni/ZnO‐Al 2 O 3 exhibited the highest deoxygenation activity and alkane selectivity, which depended on its moderate basicity. Investigations of the reaction conditions, which include reaction time, reaction temperature, H 2 pressure, and Ni loading, suggested that n ‐heptadecane was the predominant product and its content increased with reaction temperature. The reaction temperature was more important than H 2 pressure in the catalytic deoxygenation of oleic acid. Additionally, the overall reaction pathways for the conversion of oleic acid were proposed based on the product distribution for different durations and reaction rates of stearic acid, 1‐octadecanol, and stearyl stearate, in which the oxygen atoms in the oleic acid were mainly removed in the form of CO through a hydrogenation–dehydrogenation–decarbonylation reaction route. If glycerol trioleate was used instead of oleic acid, Ni/ZnO‐Al 2 O 3 exhibited a high hydrodecarbonylation activity and selectivity to n ‐heptadecane.