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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.
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页码:141 / 146
页数:6
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