Secondary inorganic components significantly
contribute to the
modification of ambient aerosol properties by forming haze or reducing
visibility. This study characterizes the water-soluble components
in PM2.5 and explores secondary inorganic aerosol (SIA)
over the air in Dhaka, Bangladesh, throughout 2019. PM2.5 samples were collected on a 24 h basis using a high-volume air sampler,
and water-soluble inorganic compositions were measured using an ion
chromatograph (IC). The observed PM2.5 may pose potential
health risks given that their 24 h mean exceeds the ambient air quality
guidelines proposed by the World Health Organization (WHO) and the
Department of Environment (DoE) of Bangladesh. Among the ions, SO4
2–, Ca2+, and NO3
– were identified as the predominant species that account
for 51, 20, and 11% of all soluble components, respectively. The soluble
ions in PM2.5 were relatively higher in the summer monsoon
(13.26 ± 6.12 μg/m3), possibly due to a combination
of rampant anthropogenic activities and the pre-monsoonal meteorology.
Humid summer plays a significant role in increasing the amount of
SIA through the liquid-phase oxidation of precursor gases. Therefore,
scavenging of ions may potentially occur (23% from the overall mean
of ions) during the long rainy monsoon season over Dhaka. The anthropogenic
origins of PM2.5, such as transportation, industry, and
construction dust, are widely present in natural sources all over
Dhaka. Dust was more sensitive to enriched PM2.5 than ions
from a seawater origin. Excluding winter data, K+ may significantly
resuspend from urban dust over Dhaka. The elements and molecular tracer
technique reveal that the potential reactive ions (e.g., Cl–, SO4
2–, and NO3
–) were more sensitive to anthropogenic human activities in Dhaka
air than to seawater and terrestrial soil. The influence of converting
vehicle fleets into compressed natural gas (CNG) run and upgrading
kiln technology on increasing SO4
2– aerosol
in Dhaka is yet to be investigated.