OXIDATIVE DEHYDROGENATION OF N-BUTANE ON IRON-ZINC OXIDE CATALYSTS

被引：49

作者：

ARMENDARIZ, H ^{[1
]}

AGUILARRIOS, G ^{[1
]}

SALAS, P ^{[1
]}

VALENZUELA, MA ^{[1
]}

SCHIFTER, I ^{[1
]}

ARRIOLA, H ^{[1
]}

NAVA, N ^{[1
]}

机构：

[1] NATL AUTONOMOUS UNIV MEXICO,FAC QUIM,MEXICO CITY 04510,DF,MEXICO

来源：

APPLIED CATALYSIS A-GENERAL | 1992年 / 92卷 / 01期

关键词：

BUTANE; IRON-ZINC OXIDE; MOSSBAUER SPECTROSCOPY; OXIDATION;

D O I：

10.1016/0926-860X(92)80277-J

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：

The oxidative dehydrogenation of n-butane to butenes over iron-zinc oxide catalysts was studied. X-ray diffraction (XRD), temperature-programmed reduction (TPR) and Mossbauer spectroscopy were used to try to identify the catalytically active phase. It was found that the presence of a zinc ferrite (ZnFe2O4) phase with a spinel structure yields high selectivity to butenes. The presence of a second phase, either alpha-Fe2O3 Or ZnO, altered the product selectivity. Alpha-Fe2O3 promoted the formation of carbon dioxide, while ZnO favored selectivity toward butadiene. Mossbauer spectroscopy indicated an electronic interaction between zinc oxide and the iron of the zinc ferrite. It is proposed that this electronic interaction may be responsible for the shift in selectivity to butadiene.

引用

页码：29 / 38

页数：10

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