TAP reactor investigation of methane coupling over samarium oxide catalysts

D.J. Statman, J.T. Gleaves, D. McNamara, P.L. Mills *, G. Fornasari, J.R.H. Ross
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引用次数: 20

Abstract

The adsorption and reaction characteristics of a Ba/Sr/Sm2O3 catalyst for methane coupling has been investigated using the TAP (Temporal Analysis of Products) reactor system. Pulsed adsorption experiments using methane, oxygen and krypton at temperatures ranging from 17°C to 800°C show that the transient response of methane is similar to that of Kr and is either not adsorbed, or weakly adsorbed on the catalyst. By contrast, oxygen is strongly adsorbed at temperatures above 500°C which suggests incorporation into the lattice with possible formation of surface anions. Pump-probe experiments in which methane and oxygen are introduced over the catalyst were also performed to investigate the effect of lifetimes of suspected surface intermediates on the relative yields of ethane and ethene. It is shown that the relative yields of both species increase with increasing values of the pulse valve time delay between introduction of the oxygen and methane. An explanation of these results using current knowledge and reasonable speculation of the mechanism is provided.

氧化钐催化剂上甲烷偶联的TAP反应器研究
采用TAP (Temporal Analysis of Products)反应系统研究了Ba/Sr/Sm2O3催化剂在甲烷偶联中的吸附和反应特性。在17 ~ 800℃的温度范围内,甲烷、氧和氪的脉冲吸附实验表明,甲烷的瞬态响应与Kr相似,要么不吸附,要么弱吸附在催化剂上。相比之下,氧在500°C以上的温度下被强烈吸附,这表明氧与晶格结合,可能形成表面阴离子。在泵探针实验中,甲烷和氧气在催化剂上被引入,以研究可疑的表面中间体的寿命对乙烷和乙烯的相对产率的影响。结果表明,两种产物的相对产率随脉冲阀引入氧和甲烷之间的时间延迟值的增加而增加。利用现有的知识和对机制的合理推测来解释这些结果。
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