甲烷化
硫化
催化作用
固溶体
水煤气变换反应
无机化学
镧
掺杂剂
化学
铈
硫黄
氧气
色散(光学)
材料科学
兴奋剂
有机化学
物理
光学
光电子学
作者
Jiaming Cheng,Yan Xu,Zhaopeng Liu,Zhenhua Li,Baowei Wang,Yujun Zhao,Xinbin Ma
标识
DOI:10.1021/acs.iecr.8b04296
摘要
A series of Mo-based catalysts supported on Ce 1– x La x O 2−δ solid solution were prepared and performed in sulfur-resistant methanation. Characterization results suggested the formation of Ce 1– x La x O 2−δ solid solution with a cubic fluorite structure. The correlation between the surface concentration of Ce 3+ and oxygen mobility was well revealed. The higher oxygen storage capacity induced by La dopant enhanced the reducibility of the MoO 3 /Ce 1– x La x O 2−δ during the sulfidation. Meanwhile, the presence of oxygen vacancy induced by Ce 3+ prompted the sulfidation of Mo species, resulting in a higher dispersion of MoS 2 . The coupling between the CO hydrogenation and water–gas-shift (WGS) reaction is important for the sulfur-resistant methanation. The apparent methanation rate is easily determined by CO hydrogenation, and WGS reaction could provide more H 2 for the CO hydrogenation. MoO 3 /Ce 0.8 La 0.2 O 2−δ catalyst exhibited the highest activity in a broad temperature regime of 450–550 °C due to its high MoS 2 dispersion and surface concentration of Ce 3+ .
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