沸石
催化作用
甲烷厌氧氧化
化学
X射线吸收光谱法
无机化学
离子交换
过渡金属
氧化还原
钯
多相催化
金属
甲烷
离子
吸收光谱法
有机化学
量子力学
物理
作者
Ida Friberg,Adam H. Clark,Phuoc Hoang Ho,Nadezda Sadokhina,Glen J. Smales,Jungwon Woo,Xavier Auvray,Davide Ferri,Maarten Nachtegaal,Oliver Kröcher,Louise Olsson
标识
DOI:10.1016/j.cattod.2020.11.026
摘要
The influence of zeolite support materials and their impact on CH oxidation activity was studied utilizing Pd supported on H-beta and H-SSZ-13. A correlation between CH oxidation activity, Si/Al ratio (SAR), the type of zeolite framework, reduction-oxidation behaviour, and Pd species present was found by combining catalytic activity measurements with a variety of characterization methods (operando XAS, NH -TPD, SAXS, STEM and NaCl titration). Operando XAS analysis indicated that catalysts with high CH oxidation activity experienced rapid transitions between metallic- and oxidized-Pd states when switching between rich and lean conditions. This behaviour was exhibited by catalysts with dispersed Pd particles. By contrast, the formation of ion-exchanged Pd and large Pd particles appeared to have a detrimental effect on the oxidation-reduction behaviour and the conversion of CH . The formation of ion-exchanged Pd and large Pd particles was limited by using a highly siliceous beta zeolite support with a low capacity for cation exchange. The same effect was also found using a small-pore SSZ-13 zeolite due to the lower mobility of Pd species. It was found that the zeolite support material should be carefully selected so that the well-dispersed Pd particles remain, and the formation of ion-exchanged Pd is minimized. 4 4 3 4 4 2+ 2+ 2+
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