The direct conversion of natural gas-in particular, itsprincipal component, methaneinto useful products has been the subject of intense study over the past decades. However, commercialization of this process is still not viable because its conversion and selectivity potentials remain low. Thus, the search continues to come up with a suitable catalyst that allows methane to be oxidized in a controlled environment to yield a high percentage of higher hydrocarbons. ZSM-5 zeolite has been known to be a suitable catalyst for olefin oligomerization. Previous studies, however, have indicated that ZSM-5 zeolites are not resistant to high temperatures. In this work, ZSM-5 was modified with copper and tungsten to develop a highly active and heat-resistant bifunctional oxidative acid catalyst. The oxidation of methane was performed over W/Cu/HZSM-5 catalyst and the results compared with the catalytic performance of W/ HZSM-5 and HZSM-5 catalysts. The metal oxide on the catalyst surface led to enhanced conversion of Hz and CO to CZ-3hydrocarbons and, hence, reduced HzO selectivity. In the liquid hydrocarbons, Cs+ selectivity increased with increasing amount of surface Bn1Jnstedacid sites. The experimental results indicated higher methane conversion and liquid hydrocarbon selectivity than that of W/3.0Cu/HZSM-5 catalyst.
[1]
Zhi-Tao Xiong,et al.
Study of W/HZSM-5-Based Catalysts for Dehydro-aromatization of CH4 in Absence of O2. II. Action of Promoters Zn and Li
,
2001
.
[2]
Zhi-Tao Xiong,et al.
Study of W/HZSM-5-Based Catalysts for Dehydro-aromatization of CH4 in Absence of O2. I. Performance of Catalysts
,
2001
.
[3]
P. Wehrer,et al.
Catalytic Activity of Bulk WO3 for the Reforming of Hexanes and Hexenes
,
2000
.
[4]
Q. Kan,et al.
The function of Cu(II) ions in the Mo/CuH-ZSM-5 catalyst for methane conversion under non-oxidative condition
,
1999
.
[5]
J. Vartuli,et al.
On the nature of framework Brønsted and Lewis acid sites in ZSM-5
,
1997
.
[6]
D. Walsh,et al.
Direct partial oxidation of methane over ZSM-5 catalyst : metals effects on higher hydrocarbon formation
,
1994
.