加氢脱氧
催化作用
木质素
化学
除氧
酚类
甲苯
纳米颗粒
氧化物
选择性
单体
化学工程
无机化学
有机化学
聚合物
工程类
作者
Kui Wu,Weiyan Wang,Haiwei Guo,Yunquan Yang,Yanping Huang,Wensong Li,Changzhi Li
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2020-03-27
卷期号:5 (4): 1330-1336
被引量:113
标识
DOI:10.1021/acsenergylett.0c00411
摘要
To enhance the catalytic activity and temper the reaction conditions in the hydrodeoxygenation (HDO) of lignin-derived phenols to arenes, a Co–MoS 2– x catalyst was proposed and prepared via a facile strategy. Co oxide was synthesized via a solvothermal method, adsorbed at the edge of MoS 2– x, and finally reduced to metallic Co via an in situ spontaneous interfacial redox reaction to form Co–MoS 2– x . In the HDO of 4-methylphenol, a 97.4% conversion with toluene selectivity up to 99.6% is obtained at the hitherto lowest reaction temperature of 120 °C. This catalyst also exhibits good versatility in catalyzing HDO of different lignin monomers and even lignin bio-oil into arenes. Notably, Co–MoS 2– x is very stable in the HDO reusability study: no deactivation was observed after recycling eight times. The high HDO activity of Co–MoS 2– x is attributed to the formation of a metal–vacancy interface and electronic transfer from Co to MoS 2– x according to the characterization results and theoretical analysis.
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