Simultaneous catalytic reduction of N 2 O and NO x for tertiary N 2 O abatement technology: A field study in a nitric acid production plant
To investigate the feasibility of the simultaneous abatement of N 2 O and NO x in a single reactor, this field study was performed in a nitric acid production plant. An Fe/BEA powder catalyst prepared by Fe ion‐exchange with steam‐treated BEA zeolite was extruded in pellets and honeycombs. In the si...
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Veröffentlicht in: | Environmental progress & sustainable energy 2019-03, Vol.38 (2), p.451-456 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | To investigate the feasibility of the simultaneous abatement of N
2
O and NO
x
in a single reactor, this field study was performed in a nitric acid production plant. An Fe/BEA powder catalyst prepared by Fe ion‐exchange with steam‐treated BEA zeolite was extruded in pellets and honeycombs. In the simultaneous reduction of N
2
O and NO
x
, the pellet‐ and honeycomb‐type catalysts showed more than a 90% and 95% conversion of N
2
O and NO
x
, respectively, at a reaction temperature between 350 °C and 380 °C which is typical for the DeNO
x
process. The catalytic performance of the pellets and honeycombs was also stable during the reactor operation period. With higher N
2
O and NO
x
conversions of over 90%, NH
3
concentration in exhaust gas streams can be reduced to satisfy domestic regulations for air pollutant emissions. Accordingly, it is suggested that the simultaneous reduction of N
2
O and NO
x
in a single reactor with the Fe/BEA catalyst may be a reasonable option for a tertiary abatement technology for nitric acid production plants.
Novelty or Significance:
The simultaneous catalytic reduction of N
2
O and NO
x
in a tail gas from a nitric acid production plant was investigated with Fe/BEA catalysts prepared by Fe ion‐exchange with steam‐treated BEA zeolite. Pellet‐ and honeycomb‐type catalysts were applied to abatement using NH
3
as the reducing agent. Over 90% of N
2
O and NO
x
from the nitric acid production process was simultaneously removed from a single reactor at a reaction temperature between 350 °C and 380 °C. © 2018 American Institute of Chemical Engineers Environ Prog, 38: 451–456, 2019 |
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ISSN: | 1944-7442 1944-7450 |
DOI: | 10.1002/ep.12979 |