Tropospheric HONO distribution and chemistry in the southeastern US
-
Published:2018-06-29
Issue:12
Volume:18
Page:9107-9120
-
ISSN:1680-7324
-
Container-title:Atmospheric Chemistry and Physics
-
language:en
-
Short-container-title:Atmos. Chem. Phys.
Author:
Ye ChunxiangORCID, Zhou Xianliang, Pu Dennis, Stutz JochenORCID, Festa James, Spolaor Max, Tsai Catalina, Cantrell ChristopherORCID, Mauldin III Roy L., Weinheimer Andrew, Hornbrook Rebecca S.ORCID, Apel Eric C., Guenther AlexORCID, Kaser Lisa, Yuan Bin, Karl ThomasORCID, Haggerty Julie, Hall Samuel, Ullmann KirkORCID, Smith JamesORCID, Ortega John
Abstract
Abstract. Here we report the measurement results of nitrous acid (HONO) and a suite of
relevant parameters on the NCAR C-130 research aircraft in the southeastern US
during the NOMADSS 2013 summer field study. The daytime HONO concentration
ranged from low parts per trillion by volume (pptv) in the free troposphere
(FT) to mostly within 5–15 pptv in the background planetary boundary layer
(PBL). There was no discernible vertical HONO gradient above the lower flight
altitude of 300 m in the PBL, and the transport of ground surface HONO was
not found to be a significant contributor to the tropospheric HONO budget. The
total in situ HONO source mean (±1 SD) was calculated as 53
(±21) pptv h−1 during the day. The upper-limit contribution from
NOx-related reactions was 10 (±5) pptv h−1, and the
contribution from photolysis of particulate nitrate (pNO3) was 38
(±23) pptv h−1, based on the measured pNO3 concentrations
and the median pNO3 photolysis rate constant of 2.0 × 10−4 s−1
determined in the laboratory using ambient aerosol samples. The
photolysis of HONO contributed to less than 10 % of the primary OH source.
However, a recycling NOx source via pNO3 photolysis was equivalent
to ∼ 2.3 × 10−6 mol m−2 h−1 in the air
column within the PBL, a considerable supplementary NOx source in the
low-NOx background area. Up to several tens of parts per trillion by volume of HONO were observed
in power plant and urban plumes during the day, mostly produced in situ
from precursors including NOx and pNO3. Finally, there was no
observable accumulation of HONO in the nocturnal residual layer and the
nocturnal FT in the background southeastern US, with an increase in the
HONO ∕ NOx ratio of ≤ 3 × 10−4 h−1 after sunset.
Funder
Division of Atmospheric and Geospace Sciences
Publisher
Copernicus GmbH
Subject
Atmospheric Science
Reference64 articles.
1. Acker, K., Moller, D., Wieprecht, W., Meixner, F. X., Bohn, B., Gilge, S.,
Plass-Dulmer, C., and Berresheim, H.: Strong daytime production of OH from
HNO2 at a rural mountain site, Geophys. Res. Lett., 33, L02809, https://doi.org/10.1029/2005gl024643, 2006. 2. Baergen, A. M. and Donaldson, D. J.: Photochemical renoxification of nitric
scid on real urban grime, Environ. Sci. Technol., 47, 815–820,
https://doi.org/10.1021/es3037862, 2013. 3. Burling, I. R., Yokelson, R. J., Griffith, D. W. T., Johnson, T. J., Veres,
P., Roberts, J. M., Warneke, C., Urbanski, S. P., Reardon, J., Weise, D. R.,
Hao, W. M., and de Gouw, J.: Laboratory measurements of trace gas emissions
from biomass burning of fuel types from the southeastern and southwestern
United States, Atmos. Chem. Phys., 10, 11115–11130,
https://doi.org/10.5194/acp-10-11115-2010, 2010. 4. Carr, S., Heard, D. E., and Blitz, M. A.: Comment on “Atmospheric hydroxyl
radical production from electronically excited NO2 and H2O”,
Science, 324, 336b, 2009. 5. de Gouw, J. and Warneke, C.: Measurements of volatile organic compounds in
the earths atmosphere using proton-transfer-reaction mass spectrometry, Mass
Spectrom. Rev., 26, 223–257, 2007.
Cited by
24 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
|
|