催化作用
钼
烟气脱硫
硫黄
化学
光催化
吸附
傅里叶变换红外光谱
产量(工程)
无机化学
材料科学
物理化学
化学工程
有机化学
工程类
冶金
作者
Chunsheng Lei,Wen Zhou,Lijuan Shen,Xiaohai Zheng,Qingguo Feng,Yi Liu,Yongpeng Lei,Shijing Liang,Dou Zhang,Lilong Jiang,Kechao Zhou
标识
DOI:10.1021/acssuschemeng.9b03274
摘要
Direct catalytic selective oxidation of H2S to sulfur at low temperature has been drawing attention. Molybdenum carbide (Mo2C), in which the excess occupied orbitals provide more back-donation chances for the adsorbents' π-orbitals, shows activity in electrocatalysis, photocatalysis, thermocatalysis, etc. that are comparable to those of noble metals. This work reports for the time the use of Mo2C and Mo2C-modified g-C3N4 for catalytic selective oxidative desulfurization. The density functional theory calculation indicates that Mo2C facilitates the adsorption of H2S molecule and the HS group. Furthermore, the Mo2C-modified g-C3N4 shows a sulfur yield of as high as 99.0% at 190 °C, much higher than that of g-C3N4 (46.0%). The good stability of the catalyst was demonstrated by X-ray diffraction, Fourier transform infrared spectra, and so on. Remarkably, the H2S conversion of the Mo2C-modified g-C3N4 remains constant (95.0%) at 190 °C for as long as 30 h. As a first demonstration using carbides in selective H2S oxidation, this work provides an opportunity to develop a novel class of potential catalysts.
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