Unexpected concentration dependence of the mass accommodation coefficient of water on aqueous triethylene glycol droplets

被引:1
|
作者
Gleichweit, Michael J. [1 ]
Mohajer, Mercede Azizbaig [1 ]
Avocat, Dominique P. Borgeaud Dit [1 ]
Diveky, Matus E. [1 ]
David, Gregory [1 ]
Signorell, Ruth [1 ]
机构
[1] Dept Chem & Appl Biosci, ETH Zurich, CH-8093 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
KINETIC MULTILAYER MODEL; EVAPORATION COEFFICIENT; CHEMICAL-REACTIONS; CONDENSATION COEFFICIENTS; MOLECULAR-BEAM; LIQUID WATER; AEROSOLS; SURFACE; VAPOR; ACID;
D O I
10.1039/d4cp00966e
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
The mass accommodation coefficient alpha M of water on aqueous triethylene glycol droplets was determined for water mole fractions in the range xmol = 0.1-0.93 and temperatures between 21 and 26 degrees C from modulated Mie scattering measurement on single optically-trapped droplets in combination with a kinetic multilayer model. alpha M reaches minimum values around 0.005 at a critical water concentration of xmol = 0.38, and increases with decreasing water content to a value of approximate to 0.1 for almost pure triethylene glycol droplets, essentially independent of the temperature. Above xmol = 0.38, alpha M first increases with increasing water content and then stabilises at a value of approximate to 0.1 at the lowest temperatures, while at the highest temperature its value remains around 0.005. We analysed the unexpected concentration and temperature dependence with a previously proposed two-step model for mass accommodation which provides concentration and temperature-dependent activation enthalpies and entropies. We suggest that the unexpected minimum in alpha M at intermediate water concentrations might arise from a more or less saturated hydrogen-bond network that forms at the droplet surface. Modulated Mie scattering measurements on single optically-trapped droplets were used to determine the mass accommodation coefficient of water on aqueous triethylene glycol aerosol droplets.
引用
收藏
页码:16296 / 16308
页数:13
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