甲烷氧化偶联
甲烷
化学
氧化磷酸化
联轴节(管道)
材料科学
无机化学
分析化学(期刊)
环境化学
冶金
有机化学
生物化学
作者
Q.S. Liu,Rui‐Sheng Wang,Ranjia Li,Xiaosheng Wang,Suoqi Zhao,C. Charles Yu
出处
期刊:ACS omega
[American Chemical Society]
日期:2024-08-17
卷期号:9 (34): 36751-36760
标识
DOI:10.1021/acsomega.4c05565
摘要
Mn-Na2WO4-based catalysts with different supports were prepared using the incipient wetness impregnation method and evaluated for their oxidative coupling of methane (OCM) reaction performance. The results demonstrated that the SiO2- supported catalyst exhibited the best catalytic performance, and the introduction of H2O further enhanced its activity. Under the conditions of a feed gas mixture of CH4/O2/H2O = 6:1:24 at 800 °C and atmospheric pressure, the CH4 conversion and C2+ selectivity over the Mn-Na2WO4/SiO2 catalyst increased from 28.4% and 77.4% (without H2O) to 33.2% and 84.9%, respectively. In contrast, the catalytic activity using TiO2 and MgO supports drastically declined. Characterizations using X-ray diffraction (XRD), in situ infrared spectroscopy (In-situ IR), X-ray photoelectron spectroscopy (XPS), hydrogen temperature-programmed reduction (H2-TPR), and oxygen temperature-programmed desorption (O2-TPD) revealed that the introduction of steam not only served as a diluent to decrease the partial pressures of the reactants CH4 and O2, thereby reducing deep oxidation reactions in the gas phase, but also interacted with surface oxygen species (O2 2-) and silica to form adjacent surface-bonded disilanol free radicals Si-OIH. This interaction facilitated the dehydrogenation and coupling of two methane molecules on the catalyst surface, resulting in the generation of C2+ products, significantly enhancing the catalytic activity and selectivity of OCM.
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