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« Previous AbstractDetection of volatile-organic-compounds (VOCs) in solution using cantilever-based gas sensors    Next AbstractModeling short-term concentration fluctuations of semi-volatile pollutants in the soil-plant-atmosphere system »

Sci Total Environ


Title:Modeling long-term uptake and re-volatilization of semi-volatile organic compounds (SVOCs) across the soil-atmosphere interface
Author(s):Bao Z; Haberer C; Maier U; Beckingham B; Amos RT; Grathwohl P;
Address:"University of Tubingen, Department of Geosciences, Holderlinstr. 12, 72074 Tubingen, Germany. Electronic address: zhongwen.bao@uni-tuebingen.de. University of Tubingen, Department of Geosciences, Holderlinstr. 12, 72074 Tubingen, Germany. Helmholtz Center for Environmental Research - UFZ, Department of Hydrogeology, Permoserstr. 15, 04318 Leipzig, Germany. College of Charleston, Department of Geology and Environmental Geosciences, 202 Calhoun Street, 29401 Charleston, SC, United States. Carleton University, Department of Earth Sciences, 1125 Colonel By Drive, K1S 5B6 Ottawa, ON, Canada"
Journal Title:Sci Total Environ
Year:2015
Volume:20150901
Issue:
Page Number:789 - 801
DOI: 10.1016/j.scitotenv.2015.08.104
ISSN/ISBN:1879-1026 (Electronic) 0048-9697 (Linking)
Abstract:"Soil-atmosphere exchange is important for the environmental fate and atmospheric transport of many semi-volatile organic compounds (SVOCs). This study focuses on modeling the vapor phase exchange of semi-volatile hydrophobic organic pollutants between soil and the atmosphere using the multicomponent reactive transport code MIN3P. MIN3P is typically applied to simulate aqueous and vapor phase transport and reaction processes in the subsurface. We extended the code to also include an atmospheric boundary layer where eddy diffusion takes place. The relevant processes and parameters affecting soil-atmosphere exchange were investigated in several 1-D model scenarios and at various time scales (from years to centuries). Phenanthrene was chosen as a model compound, but results apply for other hydrophobic organic compounds as well. Gaseous phenanthrene was assumed to be constantly supplied to the system during a pollution period and a subsequent regulation period (with a 50% decline in the emission rate). Our results indicate that long-term soil-atmosphere exchange of phenanthrene is controlled by the soil compartment - re-volatilization thus depends on soil properties. A sensitivity analysis showed that accumulation and transport in soils in the short term is dominated by diffusion, whereas in the long term groundwater recharge and biodegradation become relevant. As expected, sorption causes retardation and slows down transport and biodegradation. If atmospheric concentration is reduced (e.g. after environmental regulations), re-volatilization from soil to the atmosphere occurs only for a relatively short time period. Therefore, the model results demonstrate that soils generally are sinks for atmospheric pollutants. The atmospheric boundary layer is only relevant for time scales of less than one month. The extended MIN3P code can also be applied to simulate fluctuating concentrations in the atmosphere, for instance due to temperature changes in the topsoil"
Keywords:"Air Pollutants/*analysis Atmosphere/chemistry Environmental Monitoring/*methods *Models, Chemical Soil/chemistry Soil Pollutants/*analysis Volatile Organic Compounds/*analysis Volatilization Biodegradation Diffusion Groundwater recharge Phenanthrene Soil;"
Notes:"MedlineBao, Zhongwen Haberer, Christina Maier, Uli Beckingham, Barbara Amos, Richard T Grathwohl, Peter eng Research Support, Non-U.S. Gov't Netherlands 2015/09/05 Sci Total Environ. 2015 Dec 15; 538:789-801. doi: 10.1016/j.scitotenv.2015.08.104. Epub 2015 Sep 1"

 
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