Mineral dust is a sink for chlorine in the marine boundary layer. Sullivan, R., C., Guazzotti, S., A., Sodeman, D., A., Tang, Y., H., Carmichael, G., R., & Prather, K., A. Atmospheric Environment, 41(34):7166-7179, 2007.
abstract   bibtex   
Dust particles affect the budgets of important traces gases by providing a surface on which heterogeneous reactions can occur. The uptake of soluble species on dust alters the physical, chemical, and optical properties and the overall ability of dust to act as cloud condensation and ice nuclei. It is commonly assumed that all measured chloride in particulate filter samples is associated with sea-salt particles and any chloride in dust occurs as the result of internal mixtures of sea-salt and dust particles, formed by cloud processing. Here we show high temporal resolution data demonstrating the direct uptake of chlorine by dust via heterogeneous reaction with HCl(g). This reaction added significant amounts of chlorine to the dust particles during a major dust storm, representing 4-9% of the individual dust particle mass. Up to 65 +/- 4% of the dust particles contained chlorine due to this heterogeneous reaction during the dust front. Ignoring this process leads to an overestimation of sea-salt concentrations from bulk measurements, and an underestimation of the degree of sea-salt aging. The uptake of chloride will change the pH and hygroscopic properties of the dust and thus can influence the budgets of other reactive gases. Including this heterogeneous process in atmospheric measurements and chemical transport models will improve our ability to predict the atmosphere's composition and radiation budget with greater accuracy. (c) 2007 Published by Elsevier Ltd.
@article{
 title = {Mineral dust is a sink for chlorine in the marine boundary layer},
 type = {article},
 year = {2007},
 keywords = {Sea-salt,aerosol,asian dust,atmosphere,california,chemical transport model,chemistry,climate,heterogeneous chemistry,mineral dust,sea-salt aerosol,single-particle analysis,storm particles,sulfate,sulfur},
 pages = {7166-7179},
 volume = {41},
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 created = {2014-10-08T16:28:18.000Z},
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 abstract = {Dust particles affect the budgets of important traces gases by providing a surface on which heterogeneous reactions can occur. The uptake of soluble species on dust alters the physical, chemical, and optical properties and the overall ability of dust to act as cloud condensation and ice nuclei. It is commonly assumed that all measured chloride in particulate filter samples is associated with sea-salt particles and any chloride in dust occurs as the result of internal mixtures of sea-salt and dust particles, formed by cloud processing. Here we show high temporal resolution data demonstrating the direct uptake of chlorine by dust via heterogeneous reaction with HCl(g). This reaction added significant amounts of chlorine to the dust particles during a major dust storm, representing 4-9% of the individual dust particle mass. Up to 65 +/- 4% of the dust particles contained chlorine due to this heterogeneous reaction during the dust front. Ignoring this process leads to an overestimation of sea-salt concentrations from bulk measurements, and an underestimation of the degree of sea-salt aging. The uptake of chloride will change the pH and hygroscopic properties of the dust and thus can influence the budgets of other reactive gases. Including this heterogeneous process in atmospheric measurements and chemical transport models will improve our ability to predict the atmosphere's composition and radiation budget with greater accuracy. (c) 2007 Published by Elsevier Ltd.},
 bibtype = {article},
 author = {Sullivan, R. C. and Guazzotti, S A and Sodeman, D A and Tang, Y H and Carmichael, G R and Prather, Kimberly A},
 journal = {Atmospheric Environment},
 number = {34}
}

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