An investigation on the promoting effect of Pr modification on SO2 resistance over MnOx catalysts for selective reduction of NO with NH3
Pr-modified MnO x catalyst was synthesized through a facile co-precipitation process, and the results showed that MnPrO x catalyst exhibited much better selective catalytic reduction (SCR) activity and SO 2 resistance performance than pristine MnO x catalyst. The addition of Pr in MnO x catalyst led...
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Veröffentlicht in: | Environmental science and pollution research international 2022-03, Vol.29 (12), p.17295-17308 |
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Sprache: | eng |
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Zusammenfassung: | Pr-modified MnO
x
catalyst was synthesized through a facile co-precipitation process, and the results showed that MnPrO
x
catalyst exhibited much better selective catalytic reduction (SCR) activity and SO
2
resistance performance than pristine MnO
x
catalyst. The addition of Pr in MnO
x
catalyst led to a complete NO conversion efficiency in 120–220 °C. Moreover, Pr-modified MnO
x
catalyst exhibited a superior resistance to H
2
O and SO
2
compared with MnO
x
catalyst. After exposing to SO
2
and H
2
O for 4 h, the NO conversion efficiency of MnPrO
x
catalyst could remain to 87.6%. The characterization techniques of XRD, BET, hydrogen-temperature programmed reduction (H
2
-TPR), ammonia-temperature programmed desorption (NH
3
-TPD), XPS, TG and in situ diffuse reflectance infrared spectroscopy (DRIFTS) were adopted to further explore the promoting effect of Pr doping in MnO
x
catalyst on SO
2
resistance performance. The results showed that MnPrO
x
catalyst had larger specific surface area, stronger reducibility, and more L acid sites compared with MnO
x
catalyst. The relative percentage of Mn
4+
/Mn
n+
on the MnPrO
x
-S catalyst surface was also much higher than those of MnO
x
catalyst. Importantly, when SO
2
exists in feed gas, PrO
x
species in MnPrO
x
catalyst would preferentially react with SO
2
, thus protecting the Mn active sites. In addition, the introduction of Pr might promote the reaction between SO
2
and NH
3
rather than between SO
2
and Mn active sites, which was also conductive to protect the Mn active sites to a great extent. Since the presence of SO
2
in feed gas had little effect on NH
3
adsorption on the MnPrO
x
catalyst surface, and the inhibiting effect of SO
2
on NO adsorption was alleviated, SCR reactions could still proceed in a near-normal way through the Eley-Rideal (E-R) mechanism on Pr-modified MnO
x
catalyst, while SCR reactions through the Langmuir-Hinshelwood (L-H) mechanism were suppressed slightly. |
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ISSN: | 0944-1344 1614-7499 |
DOI: | 10.1007/s11356-021-17006-3 |