催化作用
硫黄
化学
甲烷
钯
硫酸化
无机化学
硫酸盐
吸附
X射线光电子能谱
甲烷厌氧氧化
拉曼光谱
化学工程
有机化学
工程类
物理
光学
生物化学
作者
Ya Ding,Sheng Wang,Lei Zhang,Lirong Lv,Dekang Xu,Wei Liu,Shudong Wang
标识
DOI:10.1016/j.cej.2019.122969
摘要
Catalytic combustion of methane was studied over Ce0.5Zr0.5O2 and CeO2 supported Pd (Pd/CZ and Pd/Ce) catalysts in the presence of SO2. The effect of sulfation (air including 100 ppm SO2 for 6 h at 500 °C) on the sulfur-tolerant performance of the catalysts was also investigated. Results indicated that there is a considerable promotion effect for CH4 complete oxidation on Pd/CZ catalyst, while the activity of Pd/Ce catalyst was inevitably inhibited. Further, the superior sulfur-tolerant behavior of Pd/CZ was verified through a 50 h time-on-stream stability test. Mechanistic insights into the synergistic effect between the support and Pd were unveiled by Raman, H2-TPR, XPS, NH3-TPD, DRIFTS, HAADF-STEM, etc. It was deduced that the formation of sulfates at the Pd-support interface could promote the dissociative adsorption of methane on Pd/CZ catalyst. Meanwhile, the higher relative acid strength and the acid amount were also decisive factors for the high sulfur-resistant performance. The enhanced acid strength and acid amount prevented the further formation of bulk-like sulfate species for the SO2 treated Pd/CZ catalyst, thus enhancing the sulfur-tolerant ability of the catalyst.
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