呋喃
羟甲基
催化作用
镍
碳纳米管
糠醛
有机化学
X射线光电子能谱
化学
反应速率常数
材料科学
无机化学
化学工程
纳米技术
动力学
物理
量子力学
工程类
作者
Zexing Huang,Xiaoao Sun,Wenguang Zhao,Xiaoting Zhu,Zhijuan Zeng,Qiong Xu,Xianxiang Liu
标识
DOI:10.1016/j.crcon.2022.08.001
摘要
Ni/CNTs catalyst showed superior catalytic performance in the selective hydrogenation of HMF into BHMF under a low hydrogen pressure. • Ni/CNTs catalyst was prepared and employed for the selective hydrogenation of HMF to BHMF. • High BHMF selectivity of 95.0% with an HMF conversion of 99.8% was obtained under low hydrogen pressure. • The excellent activity of the catalyst was attributed to the synergistic cooperation of Ni 0 /Ni 2+ sites of the support. • A kinetic study indicated a pseudo first order reaction with a significantly high rate constant for BHMF formation. 2,5-Bis(hydroxymethyl)furan (BHMF) is a high-value, bio-based, rigid diol that resembles aromatic monomers for the production of different polyesters. In this work, a carbon nanotubes (CNTs)-supported nickel catalyst (Ni/CNTs) was prepared and used for the selective hydrogenation of 5-hydroxymethylfurfural (HMF) to BHMF at low hydrogen pressure. The prepared catalyst was analyzed by nitrogen adsorption–desorption isotherms, X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). According to kinetic studies, the rate constant for BHMF formation is significantly larger than that for the formation of the byproduct, 5-methyl furfural (MF). At optimal reaction conditions, conversion and selectivity rates of HMF and BHMF were 99.8% and 95.0%, respectively. The mechanistic study indicated the coexistence of Ni 0 and Ni 2+ species on the catalyst surface affects the catalytic performance. A possible mechanism was proposed to describe the synergetic effects of Ni 0 and Ni 2+ . Furthermore, the catalyst can be easily separated from the reaction mixture for recycling.
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