2021/07/03 by Shihe Xu, Annette B. Vogel · 1 voice
Chemical Engineering · Engineering · Materials Science · #Odor and Emission Control Technologies #Marine Biology and Environmental Chemistry #Surface Modification and Superhydrophobicity
paper · doi:10.1016/j.chemosphere.2021.131291
openalex publication_date 2021/07/03 · openalex created_date 2025/10/10 · openalex updated_date 2026/07/29
The objective of this study was to determine snow scavenging of cVMS and its potential effect on the cVMS concentrations in snowmelt water and surrounding soil. Snow scavenging of two cVMS, octamethylcyclotetrasiloxane (D4) and decamethylcyclopentasiloxane (D5), was examined in two steps. First, sorption and desorption of D4 and D5 on snowflakes, including snow sorption coefficients (KiA), were measured against a benchmark compound, cyclopentanone, at different temperatures from 0 to −20 °C. Measurements were made using a custom-made snow chamber and 14C-labeled D4 and D5. In addition, the transfer of snow-bound cVMS to snowmelt water and surrounding soil was studied with 14C-D4 and 14C-D5-spiked snowpack placed both in a closed snow chamber and on top of a layer of frozen soil in an open chemical hood. KiA values measured in both sorption and desorption processes were very small (<10−2 m). They increased with decreasing temperature and were higher for the D5 compared to D4. The calculated gas scavenging of D4 and D5 was small because of the small KiA values, while particle scavenging of cVMS is predicted to be negligible due to their low octanol/air partition coefficients (KOA). Most importantly, almost all 14C-D4 and 14C-D5 sorbed by a snowpack was lost during the snow melting process through re-volatilization and hydrolysis and became non-detectable in snowmelt water. In short, the experimental measurements demonstrated that snow scavenging could not be a valid deposition mechanism for these volatile hydrophobic compounds.