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. 2012 May;19(4):1187-97.
doi: 10.1007/s11356-011-0635-9. Epub 2011 Oct 20.

Transformation of atmospheric ammonia and acid gases into components of PM₂.₅: an environmental chamber study

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Transformation of atmospheric ammonia and acid gases into components of PM₂.₅: an environmental chamber study

Sailesh N Behera et al. Environ Sci Pollut Res Int. 2012 May.

Abstract

Introduction: The kinetics of the transformation of ammonia and acid gases into components of PM(2.5) has been examined. The interactions of existing aerosols and meteorology with the transformation mechanism have also been investigated. The specific objective was to discern the kinetics for the gas-to-particle conversion processes where the reactions of NH(3) with H(2)SO(4), HNO(3), and HCl take place to form (NH(4))(2)SO(4), NH(4)NO(3), and NH(4)Cl, respectively, in PM(2.5).

Materials and methods: A Teflon-based outdoor environmental chamber facility (volume of 12.5 m(3)) with state-of-the-art instrumentation to monitor the concentration-time profiles of precursor gases, ozone, and aerosol and meteorological parameters was built to simulate photochemical reactions.

Results and discussion: The reaction rate constants of NH(3) with H(2)SO(4), HNO(3), and HCl (i.e., k (S), k (N), and k (Cl)) were estimated as (1) k (S) = 2.68 × 10(-4) (±1.38 × 10(-4)) m(3)/μmol/s, (2) k (N) = 1.59 × 10(-4) (±8.97 × 10(-5)) m(3)/μmol/s, and (3) k (Cl) = 5.16 × 10(-5) (±3.50 × 10(-5)) m(3)/μmol/s. The rate constants k (S) and k (N) showed significant day-night variations, whereas k (Cl) did not show any significant variation. The D/N (i.e., daytime/nighttime values) ratio was 1.3 for k (S) and 0.33 for k (N). The significant role of temperature, solar radiation, and O(3) concentration in the formation of (NH(4))(2)SO(4) was recognized from the correlation analysis of k (S) with these factors. The negative correlations of temperature with k (N) and k (Cl) indicate that the reactions for the formation of NH(4)NO(3) and NH(4)Cl seem to be reversible under higher temperature due to their semivolatile nature. It was observed that the rate constants (k (S), k (N), and k (Cl)) showed a positive correlation with the initial PM(2.5) levels in the chamber, suggesting that the existing surface of the aerosol could play a significant role in the formation of (NH(4))(2)SO(4), NH(4)NO(3), and NH(4)Cl.

Conclusions: Therefore, this study recommends an intelligent control of primary aerosols and precursor gases (NO( x ), SO(2), and NH(3)) for achieving reduction in PM(2.5) levels.

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