Reacto-Diffusive Length of N2O5 in Aqueous Sulfate- and Chloride-Containing Aerosol Particles

被引:44
作者
Gaston, Cassandra J. [1 ,2 ]
Thornton, Joel A. [1 ]
机构
[1] Univ Washington, Dept Atmospher Sci, Seattle, WA 98195 USA
[2] Univ Miami, Rosenstiel Sch Marine & Atmospher Sci, 4600 Rickenbacker Causeway, Miami, FL 33149 USA
基金
美国国家科学基金会;
关键词
SEA-SALT AEROSOL; SULFURIC-ACID; GASEOUS N2O5; HETEROGENEOUS HYDROLYSIS; REACTION PROBABILITIES; THERMODYNAMIC MODEL; NITRATE; AMMONIUM; ACTIVATION; REACTIVITY;
D O I
10.1021/acs.jpca.5b11914
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Heterogeneous reactions of dinitrogen pentoxide (N2O5) on aerosol particles impact air quality and climate, yet aspects of the relevant physical chemistry remain unresolved. One important consideration is the competing effects of diffusion and the rate of chemical reaction within the particle, which determines the length that N2O5 travels within a particle before reacting, referred to as the reacto-diffusive length (l). Large values of l imply a dependence of the reactive uptake efficiency of N2O5, i.e., gamma(N2O5), on particle size. We present measurements of the size dependence of gamma(N2O5) on aqueous sodium chloride, ammonium sulfate, and ammonium bisulfate particles. gamma(N2O5) on ammonium sulfate and ammonium bisulfate particles ranged from 0.016 +/- 0.005 to 0.036 +/- 0.001 as the surface-area weighted particle radius increased from 39 to 127 nm, resulting in an estimated l of 32 +/- 6 nm. In contrast, gamma(N2O5) on sodium chloride particles was independent of particle size, suggesting a near-surface reaction dominated the uptake of N2O5. Differences in the reactivity of the N2O5 intermediate, NO2+, with water and chloride can explain the observed dependencies. These results allow for parameterizations in atmospheric models to determine a more robust population mean value of gamma(N2O5) that accounts for the distribution of particle sizes.
引用
收藏
页码:1039 / 1045
页数:7
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