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Poorly quantified trends in ammonium nitrate remain critical to understand future urban aerosol control strategies

delete2025-05-23
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PRE
AI
R
Ryan X. Ward *
H
Haroula D. Baliaka
B
Benjamin C. Schulze
G
Gaige Hunter Kerr
J
John D. Crounse
S
Sina Hasheminassab
R
R. Bahreini
A
Ann M. Dillner
A
Armistead G. Russell
N
N. L. Ng
P
P. O. Wennberg
R
Richard C. Flagan
J
John H. Seinfeld
DOI:10.1126/sciadv.adt8957delete
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Abstract

Abstract

En 中文
Despite decades of progress in reducing nitrogen oxide (NOx) emissions, ammonium nitrate (AN) remains the primary inorganic component of particulate matter (PM) in Los Angeles (LA). Using aerosol mass spectrometry over multiple years in LA illustrates the controlling dynamics of AN and their evolution over the past decades. These data suggest that much of the nitric acid (HNO3) production required to produce AN in LA occurs during the nighttime via heterogeneous hydrolysis of N2O5. Further, we show that US Environmental Protection Agency-codified techniques for measuring total PM2.5 fail to quantify the AN component, while low-cost optical sensors demonstrate good agreement. While previous studies suggest that declining NOx has reduced AN, we show that HNO3 formation is still substantial and leads to the formation of many tens of micrograms per cubic meter of AN aerosol. Continued focus on reductions in NOx will help meet the PM2.5 standards in the LA basin and many other regions.
Keywords:
CHEMICAL SPECIATION MONITOR
PARTICULATE MATTER PM2.5
LOS-ANGELES BASIN
FINE-PARTICLE PH
ATMOSPHERIC AMMONIA
EVAPORATIVE LOSSES
EQUILIBRIUM-MODEL
ORGANIC AEROSOL
NITRIC-ACID
SULFATE

Journal

Science Advances cover
Science Advances
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12.5
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2.0W
Citations:
18.1W

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Environmental Defense Fund
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