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Surface/bulk partitioning and acid/base speciation of aqueous decanoate: Direct observations and atmospheric implications

Prisle N, Ottosson N, Öhrwall G, Söderström J, Dal Maso M, Björneholm O...(+6 more)

Atmospheric Chemistry and Physics, vol. 12, issue 24 (2012) pp. 12227-12242

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Abstract

Dilute aqueous solutions of the atmospheric organic surfactant sodium decanoate have been studied using surface sensitive X-ray photoelectron spectroscopy combined with synchrotron radiation. We studied the decanoate/decanoic acid speciation and preferential adsorption at the vapor-liquid interface, and the responses to mixing in solution with some of the most common atmospheric inorganic ions, Na+, NH4+, Cl-, and SO42-. We observe little or no influence of Na+, Cl-, or SO42- ions, on neither the relative speciation nor the individual adsorption properties of decanoate and decanoic acid. In particular, no significant salting-out effect due to common Na+ cations of the organic and inorganic salts was observed for these solutions. On the other hand, mixing with NH4+ cations resulted in a pronounced surface enhancement of decanoic acid, which is attributed to surface specific acid-base chemistry. These changes in surface/bulk partitioning and surface speciation may significantly affect properties of aqueous droplets containing decanoate/decanoic acid, and potential implications for several processes critical to the climate effects of atmospheric aerosols are discussed.

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