首页 | 本学科首页   官方微博 | 高级检索  
     检索      


A multiphase flow and multispecies reactive transport model for DNAPL-involved Compound Specific Isotope Analysis
Institution:1. Aquanty Inc., 564 Weber Street North, Unit 12, Waterloo, ON N2L 5C6, Canada;2. Department of Earth and Environmental Sciences, University of Waterloo, Waterloo, ON N2L 3G1, Canada;3. Department of Earth and Environmental Sciences, Chonbuk National University, Jeonju-si, Jeollabuk-do 561-756, Republic of Korea;4. The Earth and Environmental Science System Research Center, Chonbuk National University, Jeonju-si, Jeollabuk-do 561-756, Republic of Korea;1. 360;2. Geosyntec Consultants, Waterloo, Ontario N2L 6R5, Canada;3. Department of Earth and Environmental Sciences, University of Waterloo, Waterloo, Ontario N2L 3G1, Canada;1. Institute of Environmental Sciences, Bo?aziçi University, 34342 Istanbul, Turkey;2. Department of Environmental Engineering, Gebze Technical University, 41400 Kocaeli, Turkey;3. Department of Geological Engineering, Kocaeli University, 41380 Kocaeli, Turkey;4. Department of Environmental Engineering, Kocaeli University, 41380 Kocaeli, Turkey;5. School of Chemical Engineering and Analytical Science, the University of Manchester, Manchester, M13 9PL, UK
Abstract:This study presents a multiphase flow and multispecies reactive transport model for the simultaneous simulation of NAPL and groundwater flow, dissolution, and reactive transport with isotope fractionation, which can be used for better interpretation of NAPL-involved Compound Specific Isotope Analysis in 3D heterogeneous hydrogeologic systems. The model was verified for NAPL-aqueous phase equilibrium partitioning, aqueous phase multi-chain and multi-component reactive transport, and aqueous phase multi-component transport with isotope fractionation. Several illustrative examples are presented to investigate the effect of DNAPL spill rates, degradation rate constants, and enrichment factors on the temporal and spatial distribution of the isotope signatures of chlorinated aliphatic hydrocarbon groundwater plumes. The results clearly indicate that isotope signatures can be significantly different when considering multiphase flow within the source zone. A series of simulations indicate that degradation and isotope enrichment compete with dissolution to determine the isotope signatures in the source zone: isotope ratios remain the same as those of the source if dissolution dominates the reaction, while heavy isotopes are enriched in reactants along groundwater plume flow paths when degradation becomes dominant. It is also shown that NAPL composition can change from that of the injected source due to the partitioning of components between the aqueous and NAPL phases even when degradation is not allowed in NAPL phase. The three-dimensional simulation is presented to mechanistically illustrate the complexities in determining and interpreting the isotopic signatures with evolving DNAPL source architecture.
Keywords:Multiphase flow and transport  Multispecies reactive transport  Compound Specific Isotope Analysis  NAPL dissolution  Back-partitioning
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号