Effect of statistics of small numbers on the chemistry of trace species in atmospheric particles
- 15 December 1997
- journal article
- Published by American Geophysical Union (AGU) in Geophysical Research Letters
- Vol. 24 (24) , 3209-3212
- https://doi.org/10.1029/97gl03193
Abstract
In models of reactions occurring in atmospheric aerosol particles, calculated concentrations of some trace species often imply fractions of a molecule per particle. When this occurs, averaging rate or equilibrium expressions over a large number of particles gives results that differ from bulk solution. Two different effects are demonstrated here. In the first, the confinement of ions in submicrometer drops suppresses the dissociation of weak acids and bases relative to bulk solution. For free radicals, there is an isolation effect that suppresses radical chain termination reactions when radical concentrations are low. Under extreme non‐equilibrium conditions, half the drops contain one radical, even when bulk solution calculations indicate a concentration orders of magnitude smaller. This can greatly enhance the rates of radical chain reactions in drops relative to bulk solution. This latter effect has the potential to dramatically alter modelled rates of reactions in atmospheric particles.Keywords
This publication has 19 references indexed in Scilit:
- Heterogeneous atmospheric bromine chemistryJournal of Geophysical Research: Atmospheres, 1996
- Heterogeneous reactions in sulfuric acid aerosols: A framework for model calculationsJournal of Geophysical Research: Atmospheres, 1994
- Aqueous‐phase chemical processes in deliquescent sea‐salt aerosols: A mechanism that couples the atmospheric cycles of S and sea saltJournal of Geophysical Research: Atmospheres, 1992
- Surface ozone depletion in Arctic spring sustained by bromine reactions on aerosolsNature, 1992
- A stochastic approach to the theory of intramicellar kinetics. III. The homogeneous system limitThe Journal of Chemical Physics, 1981
- A stochastic approach to the theory of intramicellar kinetics. II. Master equation for reversible reactionsThe Journal of Chemical Physics, 1981
- A stochastic approach to the theory of intramicellar kinetics. I. Master equation for irreversible reactionsThe Journal of Chemical Physics, 1980
- Diffusion-controlled reaction kinetics in micellesChemical Physics Letters, 1979
- Exact stochastic simulation of coupled chemical reactionsThe Journal of Physical Chemistry, 1977
- A general method for numerically simulating the stochastic time evolution of coupled chemical reactionsJournal of Computational Physics, 1976