Atmospheric Chemistry and Physics (Mar 2012)

Direct N<sub>2</sub>O<sub>5</sub> reactivity measurements at a polluted coastal site

  • C. J. Gaston,
  • K. A. Prather,
  • L. M. Russell,
  • S. Liu,
  • D. A. Day,
  • O. S. Ryder,
  • T. H. Bertram,
  • T. P. Riedel,
  • J. A. Thornton

DOI
https://doi.org/10.5194/acp-12-2959-2012
Journal volume & issue
Vol. 12, no. 6
pp. 2959 – 2968

Abstract

Read online

Direct measurements of N2O5 reactivity on ambient aerosol particles were made during September 2009 at the Scripps Institution of Oceanography (SIO) Pier facility located in La Jolla, CA. N2O5 reactivity measurements were made using a custom flow reactor and the particle modulation technique alongside measurements of aerosol particle size distributions and non-refractory composition. The pseudo-first order rate coefficients derived from the particle modulation technique and the particle surface area concentrations were used to determine the population average N2O5 reaction probability, γ(N2O5), approximately every 50 min. Insufficient environmental controls within the instrumentation trailer led us to restrict our analysis primarily to nighttime measurements. Within this subset of data, γ(N2O5) ranged from γ(N2O5) are important, such as organic coatings or non-aqueous particles. The largest apparent driver of day-to-day variability in the measured γ(N2O5) at this site was the particle nitrate loading, as inferred from both the measured particle composition and the parameterizations. The relative change in measured γ(N2O5) as a function of particle nitrate loading appears to be consistent with expectations based on laboratory data, providing direct support for the atmospheric importance of the so-called "nitrate effect".