Constituent selection and performance characterization of catalysts for oxidative coupling of methane and oxidative dehydrogenation of ethane

被引:38
作者
Wan, HL [1 ]
Chao, ZS [1 ]
Weng, WZ [1 ]
Zhou, XP [1 ]
Cai, JX [1 ]
Tsai, KR [1 ]
机构
[1] XIAMEN UNIV, STATE KEY LAB PHYS CHEM SOLID SURFACE, XIAMEN 361005, PEOPLES R CHINA
基金
中国国家自然科学基金;
关键词
oxidative coupling of methane; oxidative dehydrogenation of ethane; alkaline-earth fluorides doped lanthanum oxyfluoride catalysts; defective fluoride structure; anionic vacancy; Raman spectroscopy;
D O I
10.1016/0920-5861(95)00330-4
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The catalytic property of BaF2-doped tetragonal LaOF catalysts for oxidative coupling of methane and oxidative dehydrogenation of ethane was evaluated in detail by independently varying the concentration of BaF2 in the catalysts. The results indicate that addition of BaF2 into the tetragonal LaOF significantly improves the catalytic performance of LaOF for both reactions, and the best results are observed over the BaF2/LaOF catalysts with BaF2 content of ca. 10 mol%. The XRD analysis of the fresh catalysts suggests that, for the catalysts with BaF2 content less than 15 mol%, most of the Ba2+ ions together with the accompanying F- and O2- may be dispersed in the LaOF, forming a Ba2+-doped LaOF phase in which some of the La3+ lattice points might be replaced by the less positively charged Ba2+, leading to the formation of an F-center, anion vacancies or O- species in the LaOF lattice which will be favorable to the adsorption and activation of O-2. The results of in situ Raman characterization of the surface dioxygen species over the LaOF and 10% BaF2/LaOF catalysts suggest that the improvement of alkane conversions on a BaF2-doped LaOF may be explained by the relative abundance of the dioxygen adspecies over the catalyst. While one of the possible reasons for the significant improvement of the selectivities may have resulted from the favorable effect of F- ions for the isolation of the surface oxygen adspecies.
引用
收藏
页码:67 / 76
页数:10
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