TY - JOUR
T1 - Catalytic reduction of NH4NO3 by NO
T2 - Effects of solid acids and implications for low temperature DeNOx processes
AU - Savara, Aditya
AU - Li, Mei Jun
AU - Sachtler, Wolfgang M.H.
AU - Weitz, Eric
N1 - Funding Information:
This work was supported by the Chemical Sciences, Geosciences and Biosciences Division, Office of Basic Energy Sciences, Office of Science, U.S. Department of Energy (DE-FG02-03-ER15457), at the Northwestern University Institute for Catalysis in Energy Processes. We would like to thank one of the reviewers for pointing out the possibility of the hydrolysis of NO + which is now discussed in Sections 4.1 and 4.3 . A. Savara thanks Danielle Gray for useful discussions at a BIP seminar at Northwestern.
PY - 2008/6/24
Y1 - 2008/6/24
N2 - Ammonium nitrate is thermally stable below 250 °C and could potentially deactivate low temperature NOx reduction catalysts by blocking active sites. It is shown that NO reduces neat NH4NO3 above its 170 °C melting point, while acidic solids catalyze this reaction even at temperatures below 100 °C. NO2, a product of the reduction, can dimerize and then dissociate in molten NH4NO3 to NO+ + NO3-, and may be stabilized within the melt as either an adduct or as HNO2 formed from the hydrolysis of NO+ or N2O4. The other product of reduction, NH4NO2, readily decomposes at ≤100 °C to N2 and H2O, the desired end products of DeNOx catalysis. A mechanism for the acid catalyzed reduction of NH4NO3 by NO is proposed, with HNO3 as an intermediate. These findings indicate that the use of acidic catalysts or promoters in DeNOx systems could help mitigate catalyst deactivation at low operating temperatures (<150 °C).
AB - Ammonium nitrate is thermally stable below 250 °C and could potentially deactivate low temperature NOx reduction catalysts by blocking active sites. It is shown that NO reduces neat NH4NO3 above its 170 °C melting point, while acidic solids catalyze this reaction even at temperatures below 100 °C. NO2, a product of the reduction, can dimerize and then dissociate in molten NH4NO3 to NO+ + NO3-, and may be stabilized within the melt as either an adduct or as HNO2 formed from the hydrolysis of NO+ or N2O4. The other product of reduction, NH4NO2, readily decomposes at ≤100 °C to N2 and H2O, the desired end products of DeNOx catalysis. A mechanism for the acid catalyzed reduction of NH4NO3 by NO is proposed, with HNO3 as an intermediate. These findings indicate that the use of acidic catalysts or promoters in DeNOx systems could help mitigate catalyst deactivation at low operating temperatures (<150 °C).
KW - Ammonium nitrate
KW - Ammonium nitrite
KW - DeNO
KW - NO
KW - NO
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U2 - 10.1016/j.apcatb.2007.12.008
DO - 10.1016/j.apcatb.2007.12.008
M3 - Article
AN - SCOPUS:43549114377
SN - 0926-3373
VL - 81
SP - 251
EP - 257
JO - Applied Catalysis B: Environmental
JF - Applied Catalysis B: Environmental
IS - 3-4
ER -