Structure/function relationships in Nd2O3-doped MgO catalysts for the methane coupling reaction

被引:19
作者
Burrows, A
Kiely, CJ
Hutchings, GJ
Joyner, RW
Sinev, MY
机构
[1] UNIV LIVERPOOL,LEVERHULME CTR INNOVAT CATALYSIS,LIVERPOOL L69 3BX,MERSEYSIDE,ENGLAND
[2] NOTTINGHAM TRENT UNIV,CTR CATALYSIS RES,NOTTINGHAM NG11 7NS,ENGLAND
[3] RUSSIAN ACAD SCI,INST CHEM PHYS,MOSCOW 117334,RUSSIA
基金
英国工程与自然科学研究理事会;
关键词
D O I
10.1006/jcat.1997.1591
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
MgO doped with Nd2O3 has been evaluated as a catalyst for the oxidative coupling of methane (OCM) reaction, It is demonstrated that significant improvements in methane conversion efficiency and selectivity to C-2 products (as compared to pure MgO) can be achieved. The level of catalytic improvement is shown to be dependent on the Nd2O3 concentration and the precise catalyst preparation method. Detailed transmission electron microscopy studies have been performed on the Nd2O3/MgO catalysts prepared by an impregnation route and by a number of coprecipitation methods. Six distinct neodymia morphologies on the MgO support have been identified. These are (i) crystalline thin films, (ii) Nd2O3 crystallites attached to the MgO support, (iii) isolated Nd2O3 needles, (iv) epitaxial microclusters, (v) disordered thin films, and (vi) isolated clusters. The relative proportions of these Nd2O3 morphologies in the catalysts are also shown to depend upon the neodymia loading and the preparation route. Cross-correlation between microstructural observations and catalytic performance data for these materials enable us to deduce that the disordered neodymia films, which probably contain some dissolved Mg2+ ions, are largely responsible for the improvement in OCM performance. (C) 1997 Academic Press.
引用
收藏
页码:77 / 91
页数:15
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