Highly Oxygenated Organic Nitrates Formed from NO3 Radical-Initiated Oxidation of β-Pinene

Author(s):  
Hongru Shen ◽  
Defeng Zhao ◽  
Iida Pullinen ◽  
Sungah Kang ◽  
Luc Vereecken ◽  
...  
Keyword(s):  
Nature ◽  
1947 ◽  
Vol 160 (4074) ◽  
pp. 753-754 ◽  
Author(s):  
L. PHILLIPS

2009 ◽  
Vol 52 (13) ◽  
pp. 4020-4025 ◽  
Author(s):  
Konstantin Chegaev ◽  
Loretta Lazzarato ◽  
Paolo Marcarino ◽  
Antonella Di Stilo ◽  
Roberta Fruttero ◽  
...  

2007 ◽  
Vol 50 (1) ◽  
pp. 68-74 ◽  
Author(s):  
Andreas Koenig ◽  
Kathrin Lange ◽  
Joerg Konter ◽  
Andreas Daiber ◽  
Dirk Stalleicken ◽  
...  
Keyword(s):  

Nature ◽  
1932 ◽  
Vol 129 (3268) ◽  
pp. 905-905
Author(s):  
A. S. GANESAN ◽  
V. N. THATTE
Keyword(s):  

2015 ◽  
Vol 15 (16) ◽  
pp. 9313-9325 ◽  
Author(s):  
L. Lee ◽  
P. J. Wooldridge ◽  
J. deGouw ◽  
S. S. Brown ◽  
T. S. Bates ◽  
...  

Abstract. Organic nitrates in both gas and condensed (aerosol) phases were measured during the Uintah Basin Winter Ozone Study from January to February in 2012. A high degree of correlation between total aerosol volume at diameters less than 500 nm and the particulate organic nitrate concentration indicates that organic nitrates are a consistent, if not dominant, fraction of fine aerosol mass. In contrast, a similar correlation with sub-2.5 μm aerosol volume is weaker. The C : N atomic ratio inferred from field measurements of PM2.5 and particulate organic nitrate is 34 : 1. Calculations constrained by the observations indicate that both condensation of gas-phase nitrates and heterogeneous reactions of NO3 / N2O5 are responsible for introducing organic nitrate functionality into the aerosol and that the source molecules are alkanes. Extrapolating the results to urban aerosol suggests organic nitrate production from alkanes may be a major secondary organic aerosol source.


2016 ◽  
Vol 5 (3) ◽  
Author(s):  
Suenia K P Porpino ◽  
Renata A Travassos
Keyword(s):  

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