The motion of drops of decane on horizontal poly(dimethylsiloxane) (PDMS)-coated glass surfaces resulting from a temperature gradient on the surface is studied experimentally, and a theoretical description of the thermocapillary motion of spherical-cap drops on a horizontal solid surface obtained using the lubrication approximation also is presented. The drop size and the applied temperature gradient are varied in the experiments, and the measured velocities of the drops are compared with predictions from the model. The scalings of the velocity with drop size and with the applied temperature gradient are predicted correctly by the theoretical model, even though the actual velocities are smaller than those predicted. The influence of contact angle hysteresis, which leads to a critical drop size below which drops do not move, is found to be minimal. Unlike in previous studies (Chen, J. Z.; Troian, S. M.; Darhuber, A. A.; Wagner, S. J. Appl. Phys. 2005, 97, 014906; Brzoska, J. B.; Brochard-Wyart, F.; Rondelez, F. Langmuir 1993, 9, 2220), this small critical drop size appears to be independent of the applied temperature gradient. Results also are presented on the deformation of the contact lines of the moving drops in the form of an aspect ratio, and correlated with the temperature difference across the footprints of the drops and the capillary number.

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This work shows, for the first time, that brown carbon formation is not observed in ambient particles undergoing drying.

<p>Recent laboratory studies have reported the formation of light-absorbing organic carbon compounds (brown carbon, BrC) in aqueous particles undergoing drying.  Atmospheric particles undergo cycles of humidification and drying during vertical transport and through daily variations in temperature and humidity, which implies particle drying could potentially be an important source of BrC globally.  In this work, we investigated BrC formation in ambient particles undergoing drying at a site in the eastern United States during summer.  Aerosol BrC concentrations were linked to secondary organic aerosol (SOA) formation, consistent with seasonal expectations for this region.  Measurements of water-soluble organic aerosol concentrations and light absorption (365 nm) were alternated between an unperturbed channel and a channel that dried particles to 41% or 35% relative humidity (RH), depending on the system configuration. The RH maintained in the dry channels was below most ambient RH levels observed throughout the study.  We did not observe BrC formation in particles that were dried to either RH level. The results were consistent across two summers, spanning ~5 weeks of measurements that included a wide range of RH conditions and organic and inorganic aerosol loadings.  This work suggests that mechanisms aside from humidification-drying cycles are more important contributors to ambient particle BrC loadings.  The implications of this work on the atmospheric budget of BrC are discussed.</p>