Molecular distributions of diacids, oxoacids and -dicarbonyls in
summer- and winter-time fine aerosols from Tianjin, North China:
Emissions from combustion sources and aqueous phase secondary formation
Abstract
To understand the characteristics and sources of water-soluble organic
aerosols (OA) in North China, we studied diacids, oxoacids and
α-dicarbonyls in summer- and winter-time fine (PM) aerosols collected
from Tianjin. Oxalic (C) acid found to be the most abundant diacid
species, followed by succinic (C), malonic (C) and sebacic (C) acids,
respectively. Glyoxylic (ωC) was the most abundant oxoacids followed by
pyruvic acid. Concentrations of total diacids, oxoacids and
α-dicarbonyls in winter were 2~3 times higher than those
in summer, but their mass fractions in PM were exactly the opposite. On
average, total diacids carbon accounted for 2.93% in total carbon and
3.31% in organic carbon (OC) in summer and 1.79% and 1.98%,
respectively, in winter. Their contribution to water-soluble OC was
almost same in both seasons (5.46% and 5.31%, respectively). Molecular
distributions, mass ratios of selected diacid (C, C, M, F C, Ph and C)
species and the linear relations among the selected species (including
ΣC-C and ΣC-C) and with inorganic markers (K and SO) implied that the
diacids and related compounds are mainly originated from coal combustion
and biomass burning emissions and produced in the atmosphere by both
photochemical reactions at regional scale in both the seasons and aging
during long-range transport, particularly in summer. This study also
revealed that diacids and related compounds and WSOC are increased with
increasing SO and they produced in aqueous phase, warranting the need of
further reduction in SO and NO to control the water-soluble OA loading
over North China.