茴香醚
加氢脱氧
氢解
催化作用
氢氧化物
苯
化学
煅烧
无机化学
有机化学
选择性
作者
Xingzhao Zhang,Xiaozhen Chen,Shaohua Jin,Zhijian Peng,Changhai Liang
标识
DOI:10.1002/slct.201600161
摘要
Abstract The catalytic performance of Ni/Al 2 O 3 catalysts derived from layered double hydroxide precursors with nickel ions incorporated into the brucite‐like layers was investigated for the hydrodeoxygenation (HDO) of anisole as a model compound of the lignin. Upon calcination and subsequent reduction, the well‐crystallized phase and highly dispersed Ni nanoparticles (3∼10 nm) on the support were obtained. The catalysts exhibited high activity toward the hydrogenolysis of C−O bonds and the hydrogenation saturation of aromatic ring at low temperature (200‐280 °C) and appropriate hydrogen pressure (2 MPa). The activity and selectivity of these two main reaction pathways of anisole conversion were independent of the Ni content. And the direct cleavage of C aromatic ‐O bond of anisole forming benzene as another parallel pathway prevails at increasing temperature. In addition, the catalysts are highly resistant to coking and easy to be reactivated by the utilization of the layered double hydroxide precursors.
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