丙烷
催化作用
选择性
介孔材料
乙烯
程序升温还原
化学
钒
扫描电子显微镜
拉曼光谱
无机化学
核化学
材料科学
有机化学
物理
光学
复合材料
作者
Jiaxin Song,Xiaoqiang Fan,Xuehua Yu,Lian Kong,Xia Xiao,Zean Xie,Zhen Zhao
标识
DOI:10.1002/slct.202301510
摘要
Abstract A series of vanadium‐doped mesoporous SiO 2 catalysts were prepared using a one‐pot emulsion method. The effects of VO x species with different structures on C−H bond activation and product selectivity in ethane and propane selective oxidation were investigated using X‐ray diffraction (XRD), N 2 adsorption‐desorption, scanning electron microscopy (SEM), transmission electron microscopy (TEM), Raman, ultraviolet‐visible diffuse reflectance spectroscopy (UV‐Vis DRS), hydrogen temperature programmed reduction (H 2 ‐TPR), and ammonia temperature programmed desorption (NH 3 ‐TPD) characterizations. The results revealed that the highly dispersed isolated tetrahedral VO x species on the catalyst gradually polymerized into highly dispersed oligomeric VO x species with the increased V loading. The former is beneficial for the formation of olefins and total aldehydes during the selective oxidation of propane. Oligomeric VO x species are conducive to improving the selectivity of ethylene and acetaldehyde in the selective oxidation of ethane. The highest catalytic performances for selective oxidation of ethane and propane were obtained at a temperature of 650 °C. The conversion of ethane was 41.6 %, with a corresponding yield of ethylene and acetaldehyde of 23.6 % over a 0.5 V−SiO 2 catalyst. In contrast, the propane conversion was 61.5 %, with a corresponding total yield of olefins and aldehydes of 41.3 % over a 1.0 V−SiO 2 catalyst.
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