Enhancement of aqueous sulfate formation by the coexistence of NO2/NH3 under high ionic strengths in aerosol water. (September 2019)
- Record Type:
- Journal Article
- Title:
- Enhancement of aqueous sulfate formation by the coexistence of NO2/NH3 under high ionic strengths in aerosol water. (September 2019)
- Main Title:
- Enhancement of aqueous sulfate formation by the coexistence of NO2/NH3 under high ionic strengths in aerosol water
- Authors:
- Chen, Tianzeng
Chu, Biwu
Ge, Yanli
Zhang, Shuping
Ma, Qingxin
He, Hong
Li, Shao-Meng - Abstract:
- Abstract: Current air quality models usually underestimate the concentration of ambient air sulfate, but the cause of this underestimation remains unclear. One reason for the underestimation is that the sulfate formation mechanism in the models is incomplete, and does not adequately consider the impact of the synergistic effects of high concentrations of multiple pollutants on sulfate formation. In this work, the roles of gaseous NO2, NH3 and solution ionic strength in the formation of sulfate in the aqueous phase were quantitatively investigated using a glass reactor and a 30 m 3 smog chamber, separately. The results showed that sulfate formation was enhanced to different degrees in the presence of gas-phase NO2, NH3 and their coexistence as solutes in both liquid solution and aerosol water. NH3 enhances the aqueous oxidation of SO2 by NO2 mainly by accelerating the uptake of SO2 through increased solubility. More importantly, we found that high ionic strength in aerosol water could significantly accelerate the aqueous oxidation of SO2, resulting in unexpectedly high S(VI) formation rates. We estimate that under severe haze conditions, heterogeneous oxidation of SO2 by NO2 on aerosols may be much shorter than that through gas phase oxidation by OH, aided by high ionic strengths in aerosols. Considering the existence of complex air pollution conditions with high concentrations of NO2, NH3 and aerosol water, as expected in typical urban and suburban settings, the sulfateAbstract: Current air quality models usually underestimate the concentration of ambient air sulfate, but the cause of this underestimation remains unclear. One reason for the underestimation is that the sulfate formation mechanism in the models is incomplete, and does not adequately consider the impact of the synergistic effects of high concentrations of multiple pollutants on sulfate formation. In this work, the roles of gaseous NO2, NH3 and solution ionic strength in the formation of sulfate in the aqueous phase were quantitatively investigated using a glass reactor and a 30 m 3 smog chamber, separately. The results showed that sulfate formation was enhanced to different degrees in the presence of gas-phase NO2, NH3 and their coexistence as solutes in both liquid solution and aerosol water. NH3 enhances the aqueous oxidation of SO2 by NO2 mainly by accelerating the uptake of SO2 through increased solubility. More importantly, we found that high ionic strength in aerosol water could significantly accelerate the aqueous oxidation of SO2, resulting in unexpectedly high S(VI) formation rates. We estimate that under severe haze conditions, heterogeneous oxidation of SO2 by NO2 on aerosols may be much shorter than that through gas phase oxidation by OH, aided by high ionic strengths in aerosols. Considering the existence of complex air pollution conditions with high concentrations of NO2, NH3 and aerosol water, as expected in typical urban and suburban settings, the sulfate formation mechanisms revealed in the present work should be incorporated into air quality models to improve the prediction of sulfate concentrations. Graphical abstract: Image 1 Highlights: Aqueous SO4 2− formation could be greatly enhanced with the presence of NO2 and NH3 . Higher reaction rate constants were observed duo to the higher ionic strengths. Relationship between reaction rate constant and ionic strengths was obtained. Abstract : Much higher reaction rate constants ( k ) between NO2 and SO2 were observed in aerosol water compared to bulk waterdue to higher ionic strengths ( I ); Relationship between k and I was obtained. … (more)
- Is Part Of:
- Environmental pollution. Volume 252(2019):Part A
- Journal:
- Environmental pollution
- Issue:
- Volume 252(2019):Part A
- Issue Display:
- Volume 252, Issue 1 (2019)
- Year:
- 2019
- Volume:
- 252
- Issue:
- 1
- Issue Sort Value:
- 2019-0252-0001-0000
- Page Start:
- 236
- Page End:
- 244
- Publication Date:
- 2019-09
- Subjects:
- Sulfate -- Aqueous-phase reaction -- Aerosol water -- Ionic strength -- Ammonia
Pollution -- Periodicals
Pollution -- Environmental aspects -- Periodicals
Environmental Pollution -- Periodicals
Pollution -- Périodiques
Pollution -- Aspect de l'environnement -- Périodiques
Pollution -- Effets physiologiques -- Périodiques
Pollution
Pollution -- Environmental aspects
Periodicals
Electronic journals
363.73 - Journal URLs:
- http://www.sciencedirect.com/science/journal/02697491 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.envpol.2019.05.119 ↗
- Languages:
- English
- ISSNs:
- 0269-7491
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3791.539000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 16677.xml