Nitrogen Pentoxide (Dinitrogen Pentoxide, N 2 O 5)

2016 ◽  
Author(s):  
Jack G. Calvert
2007 ◽  
pp. 78-81 ◽  
Author(s):  
N. S. Gruenhut ◽  
M. Goldfrank ◽  
M. L. Cushing ◽  
G. V. Caesar ◽  
P. D. Caesar ◽  
...  

1968 ◽  
Vol 72 (3) ◽  
pp. 1081-1082 ◽  
Author(s):  
Giorgio Liuti ◽  
Seymour Dondes ◽  
Paul Harteck
Keyword(s):  

RSC Advances ◽  
2021 ◽  
Vol 11 (42) ◽  
pp. 25841-25847
Author(s):  
Alexandr K. Kharchenko ◽  
Ruslan V. Fauziev ◽  
Mikhail N. Zharkov ◽  
Ilya V. Kuchurov ◽  
Sergei G. Zlotin

A green, safe, and economical method for the production of nitroaromatics is developed. The method comprises the use of the eco-friendly nitrating agent, dinitrogen pentoxide, and liquefied 1,1,1,2-tetrafluoroethane as the reusable reaction medium.


1927 ◽  
Vol 49 (5) ◽  
pp. 1257-1269 ◽  
Author(s):  
Warren F. Busse ◽  
Farrington Daniels
Keyword(s):  

1983 ◽  
Vol 105 (12) ◽  
pp. 3789-3793 ◽  
Author(s):  
Bruce W. McClelland ◽  
Lise Hedberg ◽  
Kenneth Hedberg ◽  
Kolbjoern Hagen

1951 ◽  
Vol 73 (10) ◽  
pp. 4542-4546 ◽  
Author(s):  
Harold S. Johnston
Keyword(s):  

1957 ◽  
Vol 79 (22) ◽  
pp. 6008-6014 ◽  
Author(s):  
Travis E. Stevens ◽  
William D. Emmons
Keyword(s):  

1982 ◽  
Vol 87 (4) ◽  
pp. 349-352 ◽  
Author(s):  
John E. Carpenter ◽  
Gerald M. Maggiora
Keyword(s):  

2018 ◽  
Author(s):  
Hui Yun ◽  
Weihao Wang ◽  
Tao Wang ◽  
Men Xia ◽  
Chuan Yu ◽  
...  

Abstract. Nitrate (NO3−) has become a major component of fine particulate matter (PM2.5) during hazy days in China. However, the role of the heterogeneous reactions of dinitrogen pentoxide (N2O5) in nitrate formation is not well constrained. In January 2017, a severe haze event occurred in the Pearl River Delta (PRD) of southern China during which high levels of PM2.5 (~ 400 μg m−3) and O3 (~ 160 ppbv) were observed at a semi-rural site (Heshan) in the western PRD. Nitrate concentrations were up to 108 μg m−3 (1 h time resolution), and the contribution of nitrate to PM2.5 reached nearly 40 %. Concurrent increases in NO3− and ClNO2 (with a maximum value of 8.3 ppbv in 1 min time resolution) were observed in the first several hours after sunset, indicating an intense N2O5 heterogeneous uptake on aerosols. The formation potential of NO3− via N2O5 heterogeneous reactions was estimated to be 39.7 to 77.3 μg m−3 in the early hours (3 to 6 h) after sunset based on the measurement data, which could completely explain the measured increase in the NO3− concentration during the same time period. Daytime production of nitric acid from the gas-phase reaction of OH + NO2 was calculated with a chemical box model built using the Master Chemical Mechanism (MCM v3.3.1) and constrained by the measurement data. The integrated nocturnal nitrate formed via N2O5 chemistry was comparable to or even higher than the nitric acid formed during the daytime. This study confirms that N2O5 heterogeneous chemistry was a significant source of aerosol nitrate during hazy days in southern China.


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