期刊
ATMOSPHERIC CHEMISTRY AND PHYSICS
卷 12, 期 24, 页码 12227-12242出版社
COPERNICUS GESELLSCHAFT MBH
DOI: 10.5194/acp-12-12227-2012
关键词
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资金
- NordForsk researcher network project [10160 NICITA]
- Knut and Alice Wallenberg Foundation (KAW)
- Swedish Research Council (VR)
- Carlsberg Foundation [2009_01_0366, 2010_01_0391]
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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