纳米反应器
催化作用
选择性
水溶液
化学
化学工程
双水相体系
镍
无机化学
光化学
有机化学
工程类
作者
Zhi Hu,Miaomiao Han,Chun Chen,Zidan Zou,Yue Shen,Zhen Fu,Xiaoguang Zhu,Yunxia Zhang,Haimin Zhang,Huijun Zhao,Guozhong Wang
标识
DOI:10.1016/j.apcatb.2022.121140
摘要
As green chemistry, aqueous-phase reactions play a vital role in modern fine chemical synthesis. Herein, an encapsulated nickel in a hollow carbon sphere ([email protected]) catalyst was constructed to effectively catalyze an aqueous-phase hydrogenation-rearrangement tandem (AP-HRT) reaction, in which water was employed as the solvent and reactant simultaneously. The activity is relevant to the HCS and Ni loading. The optimal [email protected] catalyst can release 100% furfural conversion and 99.1% cyclopentanone selectivity at 150 °C and can maintain its activity after 10 cycles of experiments. The superior catalytic performance comes from the fact that each independent [email protected] can be treated as an individual nanoreactor with a void-confinement effect, which not only reduces the side reactions due to the size-selective effect but also prevents active metal from leaching under harsh conditions. The reaction mechanism of FAL AP-HRT was further investigated via kinetic experiments combined with DFT calculations.
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