Mathematical model for hydraulically aided electrokinetic remediation of aquifer and removal of nonanionic copper     

Sadataka Shiba  Yushi Hirata  Tadachika Seno   《Engineering Geology》2005,77(3-4):305-315

One of the most cost-effective in situ technologies for soil and groundwater (i.e., aquifer) remediation is electrokinetic remediation. In electrokinetic remediation, electromigration due to electric field is combined with hydromigration due to hydraulic flow by purge water to remove pollutants from aquifers through the pore water. This study aims at investigating theoretically the role of electromigration (as active movement) of pollutants and the role of hydromigration (as passive movement) of pollutants in electrokinetic remediation, and making it clear that the control variables for electrokinetic remediation are the applied voltage and the hydraulic flow rate. These aims are pursued by construction of a mathematical model based on physico-chemical considerations and by model simulations of the electrokinetic remediation applied to the virtual aquifer polluted by heavy metals of copper sulfate. According to numerical simulations with the model: (1) heavy metal (nonanionic copper) is removed from the upstream anode region and accumulated in the downstream cathode region; (2) to carry away the heavy metal outside the aquifer (global removal), hydromigration by purge water flow is essential; and (3) electromigration contributes mainly to the redistribution of heavy metals within the aquifer (local removal and local accumulation).  相似文献   

The relation between electric and redox potential: evidence from laboratory and field measurements     

F. Timm  P. Mller 《Journal of Geochemical Exploration》2001,72(2)

In field and laboratory experiments the relationship of redox, electric, and total potential was studied. This was carried out by using different arrangements of Pt and Ag/AgCl electrodes. The total potential is obtained by placing a Pt and an Ag/AgCl electrode at considerable distance apart on the rock. The studies indicate that the total potential yields the sum of redox and electric potential. Deviations larger than a couple of mV are caused by extensive fluid–rock interactions. In the laboratory it is seen that the magnitude of the electric potential is generally not larger than the artificially produced difference of the redox potential. The former is most likely attributed to a diffusion or membrane potential. At field scale the electric potential is designated as self potential. Redox potential measurements in the field may supply information from remnants of pore fluid of the rock and thereby may be suitable to support the exploration of concealed metal deposits. Detectable are in particular the fast H⁺ ions which are released by electrochemical reactions and transported by electromigration, both of which are attributed to the presence of the so called geobattery.  相似文献   

Electrokinetic retention, migration and remediation of nitrates in silty loam soil under hydraulic gradients   总被引：1，自引：0，他引：1  

Krishnapillai Manokararajah  Ramanathan Sri Ranjan   《Engineering Geology》2005,77(3-4):263-272

Contamination of groundwater by nitrates leaching from intensive agricultural and livestock operations have become a major concern for surrounding communities that use groundwater as their water supply. High levels of nitrate in drinking water poses a significant risk to human health, i.e., methaemoglobinaemia (“blue baby” syndrome).

The traditional pump-and-treat method is ineffective in medium to fine-textured agricultural soils due to the low hydraulic conductivity. This paper presents the results of a laboratory experiment investigating the feasibility of using electrokinetic treatment in retaining, accumulating, moving and remediating nitrates in a silty loam soil under hydraulic gradients.

A hydraulic gradient of 1.25 was applied to the horizontal soil columns to simulate a groundwater movement system. The study was performed in two stages. During the first stage of the experiment, the anode located at the inflow end of the columns was able to retard the movement of nitrates even under a hydraulic gradient of 1.25. After 15 days of flow, the effluent nitrate concentration in the control column rose to 90 mg l⁻¹ while no nitrates were detected in the effluent from columns subjected to the electrokinetic treatment.

After 15 days, the polarity of the electrodes was switched and this second stage lasted another 20 days. The cathode near the inflow end promoted the conversion of nitrates entering the column to other forms. The anode near the outflow end promoted the migration and accumulation of negatively charged nitrate ions towards the outflow end. By the 12th day, the nitrate concentrations in the electrokinetically treated columns were brought down to <5 mg NO₃-N l⁻¹. Electrokinetic treatment retarded nitrate movement against a hydraulic gradient of 1.25 and effectively restored a medium-textured soil contaminated with NO₃-N.

The NO₂-N level remained below 1 mg l⁻¹ throughout the experiment. The hydraulic conductivity varied between 1.0E–7 and 3.6E–7 m s⁻¹. The current requirement varied between 3 and 6 mA.  相似文献   

Electrokinetic Restoration of Sulfate‐Accumulated Saline Greenhouse Soil     

Jung‐Min Cho  Do‐Hyung Kim  Jung‐Seok Yang  Kitae Baek 《洁净——土壤、空气、水》2011,39(12):1036-1040

Electrokinetic (EK) process was performed to restore sulfate‐originated saline soil and to evaluate the effect of treatment duration. Sulfate and potassium were the major ionic salts in the saline soil used in this study. A constant voltage gradient of 1 V/cm was applied for 8, 12, and 16 days. After EK treatment, anions and cations were transported toward anode and cathode, respectively, by electromigration. Chloride was completely removed, and 85.6% of nitrate was removed after 8 days of treatment. The increase of treatment period from 8 to 12 days had a negligible effect on the enhancement in the rate of sulfate removal; however, over 70% was removed after16 days. At the end of experiment, the electrical conductivity (EC) of the soil, an indicator of soil salinity, decreased to 1.93 dS/m from an initial value of 5.3 dS/m, and the distribution of sulfate was similar to that of EC. The operation time of 16 days was sufficient to restore the sulfate‐originated saline soil using the EK process.  相似文献   

Studying the migration behaviour of selenate in Boom Clay by electromigration     

Thomas Beauwens  Pierre De Cannire  Hugo Moors  Lian Wang  Norbert Maes 《Engineering Geology》2005,77(3-4):285-293

For the disposal of high-level waste (HLW) in a deep geological formation as Boom Clay, safety assessment studies have shown that long lived ⁷⁹Se is one of the more critical fission products. Therefore, the knowledge of its migration properties (diffusion, retention) through the geological barrier (Boom Clay) is of paramount importance. The migration behaviour of selenium strongly depends on its speciation. Under reducing conditions, selenide would be the dominant species and selenium migration would mainly be controlled by the low solubility of Se(−II)-bearing minerals. However Se species are often found in redox disequilibrium and more oxidized species might also coexist. Therefore, the study of selenate migration requires attention, as it might be the most mobile selenium species in the host rock. Electromigration experiments performed with a ⁷⁵Se-labeled selenate in Boom Clay indicate a high mobility for this species. The apparent diffusion coefficient (D_app) of selenate in Boom Clay is estimated from electromigration experiments performed under different electric fields. Using two independent approaches, the value of D_app for selenate is shown to fall in the range from 1.7×10⁻¹¹ to 6.2×10⁻¹¹ m² s⁻¹. Moreover, no reduction of selenate in Boom Clay was observed.  相似文献