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Pore Water Velocity (pore + water_velocity)
Selected AbstractsPhysicochemical factors controlling the release of dissolved organic carbon from columns of forest subsoilsEUROPEAN JOURNAL OF SOIL SCIENCE, Issue 2 2002J.-M. Münch Summary Retention of dissolved organic carbon in soil depends on the chemical and physical environment. We studied the release of organic carbon from three carbonate-free forest subsoil materials (Bs1, Bs2, Bg) in unsaturated column experiments as influenced by (i) variations of the flow regime and (ii) varied chemical properties of the irrigation solution. We investigated the effect of flow initiation, constant irrigation, interruptions to flow, and variation in the effective pore water velocity on the release of organic C. The influence of ionic strength and cation valence in the irrigation solution was studied by stepped pulses of NaCl and CaCl2. The release of C from all materials was characterized by an initial large output and a decline to constant concentrations under long-term irrigation. Interrupting the flow increased its release when flow was resumed. The release from the Bs1 material was not related to the duration of the interruption. The Bs2 material, in contrast, released organic carbon in a way that was successfully described by a kinetic first-order model. Increased pore water velocity decreased the concentrations of C in the effluent from it. The pH of the irrigation solution had negligible effects on the mobilization of C. Increased ionic strength reduced the release, whereas rinsing with distilled water increased the concentrations of C in the effluent. The response of dissolved C to pulses of weak solutions, however, was sensitive to the type of cation in the previous step with strong solutions. The results suggest that the release of organic matter in the soils depends on its colloidal properties. [source] Degradation of TCE with Iron: The Role of Competing Chromate and Nitrate ReductionGROUND WATER, Issue 3 2000Oliver Schlicker This study evaluates the potential of using granular iron metal for the abiotic removal of the organic ground water pollutant trichloroethene (TCE) in the presence of the common inorganic co-contaminants chromate and nitrate, respectively. Our long-term column experiments indicate a competitive process between TCE dechlorination and reductive transformation of chromate and nitrate, which is reflected in a significantly delayed onset of TCE dechlorination. Delay times and therefore the ranges of the nonreactive flowpaths increased with increasing experimental duration, resulting in a migration of the contaminants through the iron metal treatment zone. The present investigation also indicates that the calculated migration rates of TCE and the added cocontaminants chromate and nitrate are linearly related to the initial content of the cocontaminants. With an average pore water velocity of 0.6 m/d and a surface area concentration of 0.55 m2/mL in the column, the calculated migration rates varled between 0.10 cm/d and 5.86 cm/d. The particular similarity between the values of TCE migration and the migration of the strong oxidants chromate and nitrate and the long-term steady state of the TCE dechlorination in the absence of the chromate and nitrate indicates that these competitive transformations are the driving force for the gradual passivation of the granular iron due to the buildup of an electrically insulating Fe(III)-oxyhydroxide. Based on these passivation processes, general formulae were developed that allow a simplified approximation of breakthrough times for the contaminants TCE, chromate, and nitrate. [source] Analytical power series solutions to the two-dimensional advection,dispersion equation with distance-dependent dispersivitiesHYDROLOGICAL PROCESSES, Issue 24 2008Jui-Sheng Chen Abstract As is frequently cited, dispersivity increases with solute travel distance in the subsurface. This behaviour has been attributed to the inherent spatial variation of the pore water velocity in geological porous media. Analytically solving the advection,dispersion equation with distance-dependent dispersivity is extremely difficult because the governing equation coefficients are dependent upon the distance variable. This study presents an analytical technique to solve a two-dimensional (2D) advection,dispersion equation with linear distance-dependent longitudinal and transverse dispersivities for describing solute transport in a uniform flow field. The analytical approach is developed by applying the extended power series method coupled with the Laplace and finite Fourier cosine transforms. The developed solution is then compared to the corresponding numerical solution to assess its accuracy and robustness. The results demonstrate that the breakthrough curves at different spatial locations obtained from the power series solution show good agreement with those obtained from the numerical solution. However, owing to the limited numerical operation for large values of the power series functions, the developed analytical solution can only be numerically evaluated when the values of longitudinal dispersivity/distance ratio eL exceed 0·075. Moreover, breakthrough curves obtained from the distance-dependent solution are compared with those from the constant dispersivity solution to investigate the relationship between the transport parameters. Our numerical experiments demonstrate that a previously derived relationship is invalid for large eL values. The analytical power series solution derived in this study is efficient and can be a useful tool for future studies in the field of 2D and distance-dependent dispersive transport. Copyright © 2008 John Wiley & Sons, Ltd. [source] Solute movement through intact columns of cryoturbated Upper ChalkHYDROLOGICAL PROCESSES, Issue 13 2008M. Mahmood-ul-Hassan Abstract Cryoturbated Upper Chalk is a dichotomous porous medium wherein the intra-fragment porosity provides water storage and the inter-fragment porosity provides potential pathways for relatively rapid flow near saturation. Chloride tracer movement through 43 cm long and 45 cm diameter undisturbed chalk columns was studied at water application rates of 0·3, 1·0, and 1·5 cm h,1. Microscale heterogeneity in effluent was recorded using a grid collection system consisting of 98 funnel-shaped cells each 3·5 cm in diameter. The total porosity of the columns was 0·47 ± 0·02 m3 m,3, approximately 13% of pores were , 15 µm diameter, and the saturated hydraulic conductivity was 12·66 ± 1·31 m day,1. Although the column remained unsaturated during the leaching even at all application rates, proportionate flow through macropores increased as the application rate decreased. The number of dry cells (with 0 ml of effluent) increased as application rate decreased. Half of the leachate was collected from 15, 19 and 22 cells at 0·3, 1·0, 1·5 cm h,1 application rates respectively. Similar breakthrough curves (BTCs) were obtained at all three application rates when plotted as a function of cumulative drainage, but they were distinctly different when plotted as a function of time. The BTCs indicate that the columns have similar drainage requirement irrespective of application rates, as the rise to the maxima (C/Co) is almost similar. However, the time required to achieve that leaching requirement varies with application rates, and residence time was less in the case of a higher application rate. A two-region convection,dispersion model was used to describe the BTCs and fitted well (r2 = 0·97,0·99). There was a linear relationship between dispersion coefficient and pore water velocity (correlation coefficient r = 0·95). The results demonstrate the microscale heterogeneity of hydrodynamic properties in the Upper Chalk. Copyright © 2007 John Wiley & Sons, Ltd. [source] |