Using phosphorus doping of MoO3/ZSM-5 to modify performance in methane dehydroaromatisation

被引:15
作者
Burns, S
Hargreaves, JSJ
Pal, P
Parida, KM
Parija, S
机构
[1] Univ Glasgow, WestCHEM, Dept Chem, Glasgow G12 8QQ, Lanark, Scotland
[2] Indian Inst Petr, Council Sci & Ind Res, Refining Technol Div, Dehra Dun 258005, Uttar Pradesh, India
[3] CSIR, Resp Res Lab, Bhubaneswar 751013, Orissa, India
基金
英国工程与自然科学研究理事会;
关键词
methane; dehydroaromatisation; hydrogen; benzene; molybdenum oxide; molybdenum carbide; ZSM-5;
D O I
10.1016/j.molcata.2005.09.041
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 performance of methane dehydroaromatisation catalysts prepared by the impregnation of H-ZSM-5 with ammonium heptamolybdate and phosphomolybdic acid precursors has been found to be different. Particular attention has been paid to hydrogen production which, although the major gas-phase product of dehydroaromatisation, is generally not reported. The use of phosphomolybdate leads to lower activity catalysts. When 5 wt.% of phosphorus is added to the catalyst prepared from ammonium heptamolybdate, the activity is suppressed and H-2 is seen as the sole gas-phase product. The rate of hydrogen formation increases with time on stream passing through a maximum, which is associated with the loss of an inorganic phosphite phase from the catalyst. Bulk MoO3 and P doped MoO3 samples are observed to produce H-2 as a result of carburisation. Although the general pattern of hydrogen formation is similar to the 5 wt.% doped zeolite catalyst, in these cases gas-phase carbon oxides are also associated with the hydrogen maximum. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:141 / 146
页数:6
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