TY - JOUR
T1 - C1-C2 alkyl aminiums in urban aerosols
T2 - Insights from ambient and fuel combustion emission measurements in the Yangtze River Delta region of China
AU - Shen, Wenchao
AU - Ren, Lili
AU - Zhao, Yi
AU - Zhou, Luyu
AU - Dai, Liang
AU - Ge, Xinlei
AU - Kong, Shaofei
AU - Yan, Qin
AU - Xu, Honghui
AU - Jiang, Yujun
AU - He, Jun
AU - Chen, Mindong
AU - Yu, Huan
N1 - Publisher Copyright:
© 2017 Elsevier Ltd
PY - 2017/1/1
Y1 - 2017/1/1
N2 - We measured low molar-mass alkyl aminiums (methylaminium, dimethylaminium, ethylaminium and diethylaminium) in urban aerosols in the Yangtze River Delta region of eastern China in August 2014 and from November 2015 to May 2016. After examining artifact formation on sample filters, methylaminium, dimethylaminium and ethylaminium concentrations were quantified. The three C1-C2 aminiums exhibited a unimodal size distribution that maximized between 0.56 and 1.0 μm. Their concentrations in PM2.5 were 5.7 ± 3.2 ng m−3, 7.9 ± 5.4 ng m−3 and 20.3 ± 16.6 ng m−3, respectively, with higher concentrations during the daytime and in warm seasons. On new particle growth days, amine uptake to particles larger than 56 nm was barely enhanced. The molar ratios of individual aminium/NH4 + in PM2.5 were on the order of 10−4 and 10−3. Aminiums were thus far less to out-compete ammonium (NH4 +) in neutralizing acidic species in particle sizes down to 56 nm. Abundant nitrate (NO3 −/SO4 2− molar ratio = ∼3) and its correlation to methylaminium and ethylaminium implied that nitrate might be more important aminium salt than sulfate in urban aerosols of this area. Direct measurement of particle-phase amine emission from coal and biomass burning showed that coal burning is an important atmospheric amine source, considering coal burning is top-ranked particulate matter source in China.
AB - We measured low molar-mass alkyl aminiums (methylaminium, dimethylaminium, ethylaminium and diethylaminium) in urban aerosols in the Yangtze River Delta region of eastern China in August 2014 and from November 2015 to May 2016. After examining artifact formation on sample filters, methylaminium, dimethylaminium and ethylaminium concentrations were quantified. The three C1-C2 aminiums exhibited a unimodal size distribution that maximized between 0.56 and 1.0 μm. Their concentrations in PM2.5 were 5.7 ± 3.2 ng m−3, 7.9 ± 5.4 ng m−3 and 20.3 ± 16.6 ng m−3, respectively, with higher concentrations during the daytime and in warm seasons. On new particle growth days, amine uptake to particles larger than 56 nm was barely enhanced. The molar ratios of individual aminium/NH4 + in PM2.5 were on the order of 10−4 and 10−3. Aminiums were thus far less to out-compete ammonium (NH4 +) in neutralizing acidic species in particle sizes down to 56 nm. Abundant nitrate (NO3 −/SO4 2− molar ratio = ∼3) and its correlation to methylaminium and ethylaminium implied that nitrate might be more important aminium salt than sulfate in urban aerosols of this area. Direct measurement of particle-phase amine emission from coal and biomass burning showed that coal burning is an important atmospheric amine source, considering coal burning is top-ranked particulate matter source in China.
KW - Atmospheric amines
KW - Fuel combustion emission
KW - New particle growth
KW - Urban aerosol composition
UR - http://www.scopus.com/inward/record.url?scp=85020870223&partnerID=8YFLogxK
U2 - 10.1016/j.envpol.2017.06.034
DO - 10.1016/j.envpol.2017.06.034
M3 - Article
C2 - 28641196
AN - SCOPUS:85020870223
SN - 0269-7491
VL - 230
SP - 12
EP - 21
JO - Environmental Pollution
JF - Environmental Pollution
ER -