Chemical characteristics of size-resolved atmospheric aerosols in Iasi, north-eastern Romania: nitrogen-containing inorganic compounds control aerosol chemistry in the area

Galon-Negru, AG; Olariu, RI; Arsene, C

HERO ID

4743344

Reference Type

Journal Article

Year

2018

HERO ID 4743344
In Press No
Year 2018
Title Chemical characteristics of size-resolved atmospheric aerosols in Iasi, north-eastern Romania: nitrogen-containing inorganic compounds control aerosol chemistry in the area
Authors Galon-Negru, AG; Olariu, RI; Arsene, C
Journal Atmospheric Chemistry and Physics
Volume 18
Issue 8
Page Numbers 5879-5904
Abstract This study assesses the effects of particle size and season on the content of the major inorganic and organic aerosol ionic components in the Iasi urban area, north-eastern Romania. Continuous measurements were carried out over 2016 using a cascade Dekati low-pressure impactor (DLPI) performing aerosol size classification in 13 specific fractions over the 0.0276-9.94 mu m size range. Fine-particulate Cl-, NO3-, NH4+ , and K+ exhibited clear minima during the warm season and clear maxima over the cold season, mainly due to trends in emission sources, changes in the mixing layer depth and specific meteorological conditions. Fine-particulate SO42- did not show much variation with respect to seasons. Particulate NH4+ and NO3- ions were identified as critical parameters controlling aerosol chemistry in the area, and their measured concentrations in fine-mode (PM2.5) aerosols were found to be in reasonable good agreement with modelled values for winter but not for summer. The likely reason is that NH4NO3 aerosols are lost due to volatility over the warm season. We found that NH4+ in PM2.5 is primarily associated with SO42- and NO3- but not with Cl-. Actually, indirect ISORROPIA-II estimations showed that the atmosphere in the Iasi area might be ammonia rich during both the cold and warm seasons, enabling enough NH3 to be present to neutralize H2SO4, HNO3, and HCl acidic components and to generate fine-particulate ammonium salts, in the form of (NH4)(2)SO4, NH4NO3, and NH4Cl. ISORROPIA-II runs allowed us to estimate that over the warm season similar to 35% of the total analysed samples had very strongly acidic pH (03), a fraction that rose to similar to 43% over the cold season. More-over, while in the cold season the acidity is mainly accounted for by inorganic acids, in the warm ones there is an important contribution by other compounds, possibly organic. Indeed, changes in aerosol acidity would most likely impact the gasparticle partitioning of semi-volatile organic acids. Overall, we estimate that within the aerosol mass concentration the ionic mass brings a contribution as high as 40.6 %, with the rest still being unaccounted for.
Doi 10.5194/acp-18-5879-2018
Wosid WOS:000430947500005
Is Certified Translation No
Dupe Override 4743344
Is Public Yes
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