کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
4546613 1627050 2014 14 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Long-term mass transfer and mixing-controlled reactions of a DNAPL plume from persistent residuals
موضوعات مرتبط
مهندسی و علوم پایه علوم زمین و سیارات فرآیندهای سطح زمین
پیش نمایش صفحه اول مقاله
Long-term mass transfer and mixing-controlled reactions of a DNAPL plume from persistent residuals
چکیده انگلیسی


• Verified the applicability of Gilland–Sherwood correlations in porous media
• Evaluated how the mass transfer is enhanced by reactions
• Studied long-term reactions that cannot be tested in small-scale experiments
• Investigated the effects of mixing and additive scarcity on reactions of DNAPLs

Understanding and being able to predict the long-term behavior of DNAPL (i.e., PCE and TCE) residuals after active remediation has ceased have become increasingly important as attention at many sites turns from aggressive remediation to monitored natural attenuation and long-term stewardship. However, plume behavior due to mass loading and reactions during these later phases is less studied as they involve large spatial and temporal scales. We apply both theoretical analysis and pore-scale simulations to investigate mass transfer from DNAPL residuals and subsequent reactions within the generated plume, and, in particular, to show the differences between early- and late-time behaviors of the plume. In the zone of entry of the DNAPL entrapment zone where the concentration boundary layer in the flowing groundwater has not fully developed, the pore-scale simulations confirm the past findings based on laboratory studies that the mass transfer increases as a power-law function of the Peclét number, and is enhanced due to reactions in the plume. Away from the entry zone and further down gradient, the long-term reactions are limited by the available additive and mixing in the porous medium, thereby behave considerably differently from the entry zone. For the reaction between the contaminant and an additive with intrinsic second-order bimolecular kinetics, the late-time reaction demonstrates a first-order decay macroscopically with respect to the mass of the limiting additive, not with respect to that of the contaminant. The late-time decay rate only depends on the intrinsic reaction rate and the solubility of the entrapped DNAPL. At the intermediate time, the additive decays exponentially with the square of time (t2), instead of time (t). Moreover, the intermediate decay rate also depends on the initial conditions, the spatial distribution of DNAPL residuals, and the effective dispersion coefficient.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Contaminant Hydrology - Volume 157, February 2014, Pages 11–24
نویسندگان
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