Uptake of acetone, ethanol and benzene to snow and ice: effects of surface area and temperature

The interactions of gas-phase acetone, ethanol and benzene with smooth ice films and artificial snow have been studied. In one technique, the snow is packed into a cylindrical column and inserted into a low-pressure flow reactor coupled to a chemical-ionization mass spectrometer for gas-phase analys...

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Veröffentlicht in:Environmental research letters 2008-10, Vol.3 (4), p.045008-045008 (5)
Hauptverfasser: Abbatt, J P D, Bartels-Rausch, T, Ullerstam, M, Ye, T J
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Sprache:eng
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Zusammenfassung:The interactions of gas-phase acetone, ethanol and benzene with smooth ice films and artificial snow have been studied. In one technique, the snow is packed into a cylindrical column and inserted into a low-pressure flow reactor coupled to a chemical-ionization mass spectrometer for gas-phase analysis. At 214 and 228K, it is found for acetone and ethanol that the adsorbed amounts per surface area match those for adsorption to thin films of ice formed by freezing liquid water, when the specific surface area of the snow (as determined from Kr adsorption at 77K) and the geometric surface area of the ice films are used. This indicates that freezing thin films of water leads to surfaces that are smooth at the molecular level. Experiments performed to test the effect of film growth on ethanol uptake indicate that uptake is independent of ice growth rate, up to 2.4µmmin−1. In addition, traditional Brunauer–Emmett–Teller (BET) experiments were performed with these gases on artificial snow from 238 to 266.5K. A transition from a BET type I isotherm indicative of monolayer formation to a BET type II isotherm indicative of multilayer uptake is observed for acetone at T≥263K and ethanol at T≥255K, arising from solution formation on the ice. When multilayer formation does not occur, as was the case for benzene at T≤263K and for acetone at T≤255K, the saturated surface coverage increased with increasing temperature, consistent with the quasi-liquid layer affecting adsorption prior to full dissolution/multilayer formation.
ISSN:1748-9326
1748-9326
DOI:10.1088/1748-9326/3/4/045008