Electrokinetic Treatment Research Articles

A novel test set up to study three-dimensional electrokinetic dewatering of dredged soil

The dredged soil obtained from maintenance activities of water bodies has emerged as a potential alternate fill material for infrastructure development. However, dredged soil requires stabilization due to high initial water content, low shear strength and high compressibility. Among several methods, stabilization of dredged soil by using electrokinetics is one of the effective ground improvement techniques that uses electric field to dewater and strengthen the soil. In this context, a series of experiments were conducted on dredged soil by using a combination of electrokinetic treatment with and without 6 kPa seating pressure (viz., low surcharge). A customized and patented electrokinetic dewatering (EKD) test set up was used for the three-dimensional electrokinetic treatment of soil. The potential difference (in the range of 6 V–48 V) within the soil was achieved by inserting stainless steel pipes of 21.4 mm outer diameter, 1.2 mm thickness, and 170 mm length. Two control tests (with and without seating pressure of 6 kPa) also were performed to understand the effectiveness of EKD. From the study, up to 1057% and 427% increase in dewatering was noted in EKD tests due to application of 24 V (optimum voltage noted in EKD tests) as compared to control tests, without and with seating pressure, respectively. Further, seating pressure with EKD resulted in effective control of crack formation in the dredged soil and uniform improvement in shear strength along the depth (up to 95 kPa). The combination of low surcharge with EKD, adopted in the study, is also expected to yield lower differential settlement, and hence better performance of geotechnical structures built on improved dredged soil. The novel 3-dimensional patented EKD test setup with Arduino-programmed automatic water pumping enables collecting and accurately measuring dewatered effluent volume, performing cone penetration tests on undisturbed soil, and collecting soil samples for determination of water content/physiochemical properties from different locations. Overall, the developed EKD setup can be utilized for evaluating the effectiveness and adopting real-time progress management for EKD or other ground improvement methods, and remediation of sludge, mine tailings, dredged sediments, and contaminated soils.

Electroosmotic permeability in kaolinite and CaCO3 poultice mixtures

Electrokinetic treatment of masonry for desalination or electroosmotic dewatering depends on a poultice, in which the electrodes are placed, which fulfills several purposes. Poultice composed of kaolinite and CaCO3 have been shown to have good workability and high pH buffering capacity. In this work, the electroosmotic (EO) permeability is studied in different kaolinite - CaCO3 mixtures. In addition, the effect on EO of using NaCl as a mixing solution is investigated. A special cell is used to test the EO in the specimens. A phenomenological approach, based on the potential gradient and the flux of solution, was used to calculate the EO flow rate and EO permeability coefficient. Results showed that by increasing the concentration of CaCO3 in the poultice mixture, the EO flow rate decreased and the poultice with 80 % CaCO3 and more did not have any EO flow. Furthermore, the ionic strength in the mixing solution decreases the EO flow rate.

Insights into processes and consequent metal(loid) behavior in dredged estuarine sediments upon electrokinetic treatment

The use and reuse of natural and waste materials after treatment has become increasingly crucial as a means of achieving sustainable and environmentally-friendly solutions, and is part of a broader trend towards embracing circular economy principles. This study aims to understand the behavior of different elements (metal(loid)s and non-metals) and minerals during and after electrokinetic remediation (EKR) and to develop an effective approach to monitor its progress and overcome unwanted occurrences. In this regard, estuarine sediments, collected from Tancarville (Seine River estuary, France), were electrokinetically treated using a 64 L laboratory reactor; treatment was done 8 h per day for 21 days. The physico-chemical properties (pH, electric conductivity, and oxido-reduction potential) and current were monitored during treatment. The spatial evolution of the physico-chemical, physical (grain size distribution), mineral (mainly carbonates), organic, and elemental (As, Ca, Cl, Mg, Na, Pb, Sr, Zn, and Zr) characteristics was studied to assess the treatment efficiency. The results showed that the acidic conditions in the anodic sediments caused the dissolution of carbonates (calcite, dolomite, and aragonite), resulting in a considerable reduction in As, Zn, and Pb. Additionally, Cl as well as electric conductivity were significantly reduced from most sediments, which is essential in agricultural practices. Furthermore, materials had precipitated and settled in the anolyte and catholyte chambers, which acted as sorbents for elements that were released from the sediments (mainly Zn and As). Finally, three distinct phases occurred during treatment and were mainly linked to the current intensity and electric conductivity on the one hand, and the dissolution of carbonates and metal(loid) release on the other. This approach can be used to treat sediments and other media to improve the overall efficiency of remediation processes and create an end product with desired characteristics.

Migration and morphological transformation patterns of heavy metals on sludge cells and extracellular polymeric substances (EPS) under the influence of different treatments.

The impediment of sludge resource utilization stems from the presence of heavy metals within the sludge matrix. To optimize heavy metal removal techniques from undried sludge, it is essential to study the distribution of heavy metals in the sludge flocs structure and the changes in morphology in the sludge cells after different treatments. In this study, the sludge was subjected to chemical treatments using citric acid (CA), EDTA, and saponin, as well as electrokinetic treatment at 2 V/cm. The distribution and migration of Cu, Ni, and Zn in sludge flocs after various treatment methods were analyzed. The heavy metals were found to migrate from intracellular to extracellular polymeric substances (EPS) without causing extensive sludge cell lysis. They gradually diffused outward with the dispersion of the EPS layer. The migration efficiency of the three heavy metals in the sludge flocs was Zn, Ni, and Cu. This was mainly related to the initial distribution and morphology of the heavy metals. Under the influence of chemicals and an electric field, the acid-soluble and reducible heavy metals in the cells partially migrated to the EPS, while the stable heavy metals transformed into an unstable state. Furthermore, the order of chemical reagents in terms of their effect on the migration efficiency of heavy metals was CA > EDTA > Saponin, owing to the varying binding strengths of heavy metals and their impact on the degree of loosening of the EPS. Especially after CA treatment a greater proportion of Cu, Ni, and Zn were transferred from the cells to the EPS. The acidification effect near the anode during electrokinetic treatment intensifies the migration of heavy metals. This study provides basic research for subsequent engineering optimization aimed at removing heavy metals from sludge.

Bioavailability enhancement of petroleum-contaminated soil by electrokinetic remediation

The Electro kinetic Remediation Technology (EKR) is recognized as the most potential remediation technology for soils with low permeability, like clay soil characteristics. Electrokinetic treatment could increase the bioavailability of contaminants in bioremediation petroleum-contaminated soil. The study, “Bioavailability enhancement of petroleum contaminated soil by electrokinetic remediation,” is experimental research in a laboratory to improve the bioavailability of petroleum hydrocarbons on clay during bioremediation with initial treatment using electrokinetic remediation techniques, finding optimum electrokinetic operating conditions of remediations, and analyzing the mechanism of remediation process in contaminated soil. Bioavailability enhancement was studied for 35 days. Polluted soil was treated with an electrokinetic box test (17cm×12cm×10cm), and DC power was used for 48 hours. Total Petroleum Hydrocarbon (TPH) concentration was determined by gravimetric methods. The results showed that the characteristics of the soil samples were dominated by 49.31% clay. The initial concentration of TPH in polluted soil is 3.7%. The electrokinetic applications during 48 hours and followed by bioremediation for 35 days those processes removed TPH up to 80.74 % (from 33780.66 mg HC (kg dry w)-1 to 6506.155176 mg HC (kg dry w)-1. There is an increase in bioavailability indicated by the rise in bacterial populations and an increase in biodegradation after electrokinetic remediation. With this approach, bioavailability has been increased by 70.18%. Bio-electrokinetic remediation is the recommended method for polluted clay soils with low bioavailability.

Coupling electrokinetic technique with hydrothermal carbonization for phosphorus-enriched hydrochar production and heavy metal separation from sewage sludge

Hydrothermal carbonization is a promising treatment technology for wet organic solid wastes, due to its energy-efficient production of functionalized carbonaceous materials. However, the usage of sewage sludge (SS) derived hydrochar as phosphorus (P) fertilizer for agricultural soil is inhibited by the presence of heavy metals (HMs). Appropriate HM removal technology is required prior to its land application. In this study, an innovative FeCl3-assisted electrokinetic technique coupling with hydrothermal carbonization (FEK–HTC) is proposed to produce SS hydrochars with reduced HM content and increased P-retention. FEK–HTC treatment showed synergistic effects in terms of P retention and HM content reduction (56–64 % for Ni, Cu, and Zn). Furthermore, the toxicity of the remaining HMs was dramatically reduced, e.g., by 39.35 % in the case of Zn. Additionally, FEK–HTC transformed P species in hydrochars into highly bio-available form. Electrokinetic treatment resulted in decreased pH values of SS feedstock and promoted the solubilization and erosion of Ca-associated P, resulting in higher non-apatite inorganic phosphorus contents (12.47 to 23.19 mg·g−1) compared to hydrochars from untreated sludge. The P migration patterns during the FEK-HTC treatment were assessed based on the combined result of chemical extraction, 31P NMR, X-ray absorption near edge structure (XANES), and diffusive gradients in thin film (DGT). DGT analysis showed that the addition of treated hydrochars greatly increased the available P content in the soil. The results provide new insights into applying FEK-HTC technique for SS management.

Monitoring Tools and Strategies for Effective Electrokinetic Nanoparticle Treatment

Nanoparticles are increasingly being used by industry to enhance the outcomes of various chemical processes. In many cases, these processes involve over-dosages that compensate for particle losses. At best, these unique waste streams end up in landfills. This circumstance is inefficient and coupled with uncertain impacts on the environment. Pozzolanic nanoparticle treatments have been found to provide remarkable benefits for strength restoration and the mitigation of durability problems in ordinary Portland cement and concrete. These treatments have been accompanied by significant particle losses stemming from over-dosages and instability of the colloidal suspensions that are used to deliver these materials into the pore structure. In this study, new methods involving simple tools have been developed to monitor and sustain suspension stability. Turbidity measurement was introduced to monitor the progress of electrokinetic nanoparticle treatment. This tool made it possible to amend a given dosing strategy in real time while it remains possible to make effective treatment adjustments. By monitoring the particle stability and using pH and electric field controls to avoid suspension collapse, successful electrokinetic treatment dosage strategies were demonstrated using 20 nm NALCO 1056 alumina-coated silica particles. These trials indicated that turbidity measurements could track the visually imperceptible phenomena of particle flocking early on at the inception of its development. Suspensions of these nanoparticles were successfully delivered into 5 cm diameter by 10 cm tall hardended cement paste (HCP) specimens by monitoring fluid turbidity along with the specific gravity and using these values to guide the active management of the treatment dosage and pH. Under this new strategy, these losses were reduced to 5% as compared to the 80% losses associated with other treatment approaches. The relationship between the turbidity and the specific gravity was found to be linear. These plots indicated regions of turbidity and specific gravity that were associated with particle flocking. The tools, guidelines, and strategies developed in this work made it possible to manage efficient (low-particle-loss) electrokinetic nanoparticle treatments by signaling in real time when adjustments to electric field, pH, and particle dosage increments were needed.

Multiscale evolution observation of the pore structures of porous media under an electrokinetic treatment

Direct current (DC) stimulation is a promising electrokinetic method for enhancing oil recovery in porous media, especially in tight sandstones, due to the more remarkable effect of electroosmosis in materials with narrower pore throats. However, an interesting reversal of enhanced oil recovery (EOR) occurs in which oil recovery begins to decrease with DC voltages; this phenomenon hinders the application of this electrokinetic technology in petroleum industry. To date, the reason for this phenomenon remains unclear. Thus, in this study, we applied nuclear magnetic resonance (NMR) and in-situ scanning electron microscope (SEM) methods to investigate the underlying mechanisms. We classified and inspected the evolution of pore structures in tight sandstones at multiple scales ranging from the nanoscale to micron scale as the strength of DC voltage increases. The effects of both low DC and high DC voltages were analyzed in detail. Results show that the size and number of nanopores increased as the DC voltage increases. A low DC voltage can transform submicropores to micropores, and a high DC voltage can fasten this transformation. Furthermore, a low DC voltage increased the number and size of micropores, but a high voltage decreased the number and size of micropores. This study provides insights into changes in the pore structures of reservoir rocks under the treatment of the DC voltage, helping develop DC voltage-related technologies to recover hydrocarbons from porous media.

Mixing Behavior and Electrical Conductivity of Diisopropyl Amine-Water Surfactantless Emulsions: Implications for the Electrokinetic Purification of Water

The water pollutant diisopropylamine (DIPA) creates surfactantless emulsions in water. DIPA droplets bear a negative electrostatic charge, as demonstrated by electrophoretic measurements. Sodium salts (NaCl and Na2SO4) decrease their charge, leading to droplet coalescence and separation into bulk layers, depending on the salt and DIPA percentages. Attenuated total reflectance – Fourier transform infrared spectroscopy (ATR-FTIR) show that the DIPA concentration in the water rich phase is below 10wt% DIPA when adding 2wt% Na2SO4 (relative to the mixture) to mixtures of 20wt%, 40wt% and 50wt% DIPA (relative to water). The same occurs when adding 2% NaCl to mixtures of 30wt%, 50wt% and 70wt% DIPA (relative to water). DIPA-water mixtures are electrically conductive and can be separated by subjecting them to an electric field (electrokinetic separation). Without salts, the concentration of DIPA in 30wt% DIPA could be reduced by ≈20wt% after 60mins treatment using a differential voltage = 12V. NaCl (0.25wt% relative to water) improved efficiency. After 15mins, the percent decrease in DIPA was ≈50wt%. Electrokinetic treatment targets exclusively contaminants dispersed in water. DIPA sorbs onto clay, alumina and iron oxide minerals, whereas it does not sorb onto gypsum and limestone. Therefore, the in situ electrokinetic separation of DIPA can be most successfully applied in aquifers where the dominant minerals are gypsum and limestone.

Evaluation of the Suitability of Electrokinetic Treatment to Desalinate the Limestone of the Tomb of Cyrus, a UNESCO World Heritage Site in Iran

The tomb of Cyrus the Great, founder of the Persian Empire, is considered one of the most important monuments of Iran. Its advanced state of deterioration motivated the need to carry out a study focused on analyzing the possible damage caused by the presence of soluble salts, and to assess the suitability of an electrokinetic treatment for their extraction. Preliminary diagnostics carried out on stone samples taken from the tomb confirmed that it is affected by the action of soluble salts, and especially by the presence of nitrates and sulfates. The effectiveness and possible harmful effects caused by electrokinetic treatment were evaluated, under laboratory conditions, using the same limestone that makes up the tomb. The obtained results show that this treatment, in a short period of time, reduces the ionic content, reaching high percentages of anion extraction, without causing any damage, which indicates that it is suitable for this type of stone.

Effect of electrokinetic process on in situ stabilization and detoxification of arsenic-contaminated soil with high content of calcium

Owing to the high risk of human exposure to arsenic-contaminated soil, reducing its toxicity is essential. This study used the electrokinetic (EK) process with iron-rich electrodes to synchronously achieve the accumulate, stabilize and detoxify soil arsenic. Changes in arsenic valence, leaching toxicity, and microbial communities related to toxicity were comprehensively considered. The results demonstrated that arsenic was mainly transported toward the anode and accumulated by electromigration owing to the negatively charged arsenic anions under EK conditions. The cathode approaching effectively promote arsenic movement to the anode; the largest As(T) transportation rate of 30.61% was achieved near the cathode (S4). The transportation ratio of As(III) was 1.84 times more than that of As(V). The As(III) content and leaching toxicity of soil arsenic in all treatments decreased after applying the EK process. In particular, the anode approaching effectively elevated the average ratios of soil As(III) oxidation and stabilization to 37.88% and 61.73%, respectively. Correspondingly, the total phospholipid fatty acid content increased substantially after EK treatment and showed a pollution stress elimination effect. The electrokinetic effect can essentially cause highly active and easily migrated arsenic to accumulate near the anode and middle sections. The electric field mediated iron mineralization and stabilized arsenic by oxidizing As(III) and reacting with newly formed iron-rich phases (S). Meanwhile, the electric field regulated the form of soil calcium from CaCO3 to CaSO4 and caused calcium-bound arsenic to change to a more stable form. According to these results, in situ stabilization and detoxification of arsenic-contaminated soil can be realized by the EK process, avoiding stabilizer addition and excavation.

Sorption of modified clay minerals in pore solution of fired clay brick under pulsed current

This experimental study examines the influence of salt ions from poultice compositions entered into the contaminated fired clay brick with applied continuous and pulsed DC current across contaminated brick sample. The concentration of salt ions in the brick samples after electrokinetic (EK) treatment was also determined. For this purpose, the brick samples were intentionally contaminated with 15 g/kg of sodium chloride (NaCl) for 10 days. Subsequently, a series of experiments were conducted utilizing electrokinetic treatment by the application of different poultices. During electrokinetic experiments, a constant DC voltage of 9 V was applied across electrodes. The results show that by employing buffering elements in kaolin clay poultice; only 55 % of Cl− ions were removed with energy consumption of 219Wh in the presence of pulsed DC current, which is very low as compare to conventional continuous DC current having (up to 84 %) removal efficiency of Cl− ions but with energy consumption of 301Wh. According to existing results, further experimental development is needed to improve the desalination efficiency and reduce the energy consumption using pulsed DC current in order to expand the application scope of this work.

Genetic programming-based predictive model for the Cr removal effect of in-situ electrokinetic remediation in contaminated soil

Soil electrokinetic remediation is an emerging and efficient in-situ remediation technology for reducing environmental risks. Promoting the dissolution and migration of Cr in soil under the electric field is crucial to decrease soil toxicity and ecological influences. However, it is difficult to establish strong relationships between soil treatment and impact factors and to quantify their contributions. Machine learning can help establish pollutant migration models, but it is challenging to derive predictive formulas to improve remediation efficiency, describe the predictive model construction process, and reflect the importance of the predictors for better regulation. Therefore, this paper established a predictive model for the electrokinetic remediation of Cr-contaminated soil using genetic programming (GP) after determining the characteristic parameters which influenced the remediation effect, described the model's adaptive optimization process through the algorithm's function, and identified the sensitivity factors affecting the Cr removal effect. Results showed that the Cr(VI) and total Cr concentrations predicted by GP were in satisfactory agreement with the experimental values, 92% of the training data and 90% of the validation data achieved errors within 1%, and could fully reflect the target ions’ content variation in different soil layers. By substituting the above prediction formulas into Sobol sensitivity analysis, it was determined that conductivity, pH, current, and moisture content dramatically affected the Cr content variation in distinguished regions. For overall contaminated area, the system current and soil pH were the most sensitive factors for Cr(VI) and total Cr contents. Remediation efforts throughout the contaminated area should focus on the role of current versus soil pH. GP and sensitivity analysis can provide decision support and operational guidance for in-situ soil electrokinetic treatment by establishing a remediation effect prediction model, expediting the development and innovation of electrokinetic technology.

Participation influence of silicate on the temporal and spatial distribution of chloride electromigration in the electrokinetics of municipal solid waste incineration fly ashes

The chloride (Cl) content in cement production and the other derivate products has been strictly restricted to avoid the corrosion of steels in building construction, which significantly narrows the possible utilization choices of Cl-abundant municipal solid waste incineration (MSWI) fly ashes. The reduction of soluble Cl from the source materials becomes an important prerequisite for efficient resource utilization of MSWI fly ashes. In this study, an electrochemical platform was constructed to investigate the potential pathways of the migration and transformation of Cl species in silicate-participated MSWI fly ashes during electrokinetic (EK) treatment. The factors including the operating time, voltage, and mass ratio of silicate to fly ashes were adjusted to evaluate the changes in pH, current, and Cl distribution. Each treated fly ash in the sampling area was evenly cut into 3 layers and 72 parts to accurately determine the distribution of Cl in the electrolyzer. More Cl- ions in the surface layer were electromigrated to the anode than those in the middle and bottom layers. The addition of silicate enhanced electromigration and improved the distribution uniformity of Cl species in the sampling area. The reduction in Ca2+ electromigration with the formation of C-S-H caused by the silicate guaranteed the continuous transfer and reactions of Cl- anions in the EK treatment.

Effect of electric current on porosity of concrete

The paper describes the influence of electric current on the porosity of concrete samples after electrically accelerated tests and other electrokinetic treatments. Three different concrete mixtures consisting of CEM I 42.5R, CEM II / A-M(S-LL) 42.5R, and CEM I 42.5R with 10 % replacement of cement by microsilica were examined. Direct current (DC) test was performed on fully saturated samples. The samples were loaded with a constant voltage of 20 V for 24 hours in chambers filled with NaOH solution. The changes in porosity were examined using mercury intrusion porosimetry (MIP), scanning electron microscopy (SEM), and open porosity (OP). The results of open porosity indicate an increase in porosity for all mixtures measurements of ∼0.6 %–2 % for treated samples. The MIP showed increase of volume of pores with radius smaller than 0.01 μm after DC test. According to X-ray diffraction (XRD) and Thermogravimetric analysis (TGA) there was ∼2 % less calcite after DC test.

NaHCO3 synergistic electrokinetics extraction of F, P, and Mn from phosphate ore flotation tailings

In this study, the NaHCO3 synergistic electrokinetic method was used to remove F, P, and Mn from phosphate ore flotation tailings (PTs). First, using PHREEQC simulation calculations, the occurrence forms of P, F, and Mn in the PTs were determined. Thereafter, under various electrokinetic treatment conditions, the variation trends between pH and the different forms of various elements in interstitial solutions of the PTs were analyzed. The influence of various electrokinetic treatment methods on conductivity and pH distribution was thoroughly investigated. The difference in P concentration between the cathode and anode chambers was 21.42 mg/L, the removal efficiency of Mn was 71.43 %, and the leaching of F was inhibited. Dissolved impurities migrated to the electrode chamber during electrokinetic treatment primarily because of electromigration and electro-osmotic flow. During the 1.00 M NaHCO3-enhanced electrokinetic treatment in the cathode chambers, in 360 min, P and F concentrations increased from 3.51 mg/L to 57.28 mg/L and 2.073 mg/L to 29.38 mg/L, respectively. Solution-precipitation of hydroxide or carbonate minerals was determined to be an important mechanism for P, F, and Mn stabilization. This study demonstrated that the NaHCO3 synergistic electrokinetic method is suitable for removing F, P, and Mn from PTs. The findings of this study provide insights for developing novel technologies for the clean treatment and high-value utilization of PTs.

A new method for assessment of electro-osmotic permeability through the integration of theoretical and experimental ion flux in electrokinetic processes

Electrokinetic (EK) technology is promising for removing heavy metals from contaminated unsaturated soils. It is crucial to accurately determine the unsaturated electro-osmotic permeability for predicting the efficiency of EK treatment, optimizing treatment strategies, and accurately predicting the distribution of contaminant concentrations. However, the current approach of estimating unsaturated electro-osmotic permeability, which involves measuring effective voltage, drainage volume, and performing exponential fitting, fails to address the issue of uneven voltage gradient distribution during EK treatment. Herein, a novel method was presented for estimating the electro-osmotic permeability of unsaturated porous media. This method quantifies the electro-osmotic flow in an unsaturated porous medium by considering the difference in mass-transfer efficiency (MTE) between real (with electro-osmotic flow) and hypothetical cases (without electro-osmotic flow). This difference serves as a metric for estimating the electro-osmotic permeability. Results revealed a linear relationship between the electro-osmotic permeability and the product of volumetric moisture content and tortuosity, with the slope related to the ionic mobility of target ions, hypothetical and actual MTE. To validate this method, hexavalent Cr (Cr(VI)) was selected as the target contaminant and six EK experiments were conducted with varying initial volumetric moisture content. The feasibility of the method was evaluated by fitting the results of these experiments to obtain the specific slope of the porous medium used. Compared to the existing effective voltage–drainage volume–exponential fitting method, the proposed method offers several advantages. First, it effectively addressed the issue of nonuniform voltage distribution during EK treatment in the unsaturated porous medium. Second, it overcame the problem of a nonzero electro-osmotic permeability at zero volumetric moisture content in the exponential empirical formula. Third, the proposed method was based on theoretical derivations instead of relying solely on empirical fitting. Finally, the proposed method does not require a prior estimate of the saturated electro-osmotic permeability of the porous medium.

Copper removal from sediment by electrokinetic treatment with electrodes in a hexagonal configuration

AbstractThis study was conducted to examine the effectiveness of removing Cu from sediment by electrokinetic (EK) treatment with electrodes in a hexagonal configuration, and whether water leached can be reused. Three experiments were performed (e1: continuous application of electricity, e2: no electricity at night, e3: application of solar panels) to evaluate the impact of the absence of electricity during night and the variations that may occur during the day when solar panels were used on the efficiency of the treatment. At the end of the treatments, 2–13% more Cu was detected in the cathode region (locations 5 and 10) compared to the initial concentration. Furthermore, based on the calculated mass balance, we concluded that Cu was bound to the electrode surface. In the remaining EK cell locations, the Cu content was reduced by 50–60% for e1, e2, and e3. For field application, treatment e3, in which solar panels are applied, is recommended, since there are no significant differences in the achieved efficiencies. A significant advantage of the treatment from an ecological point of view is reflected in the absence of an acidification effect. In this study, we also applied a model which showed satisfactory agreement with the experimental results. Analyses of leached water after electrokinetic treatments, e1, e2, e3, indicate that this water has a potential for irrigation use of agricultural land, aiming to meet the goals of the circular economy.

Integrated application of green zero-valent iron and electrokinetic remediation of metal-polluted sediment.

In recent years, more focus has been placed on integrated metal removal processes. Electrokinetic (EK) treatment is superior to other technologies because it can be applied to a variety of mediums. Green nanoparticles, on the other hand, have the potential to significantly reduce pollutant concentrations in a short period of time. In this study, we investigated the possibility of combining green zero-valent iron (nZVI) with EK on Cd and Zn-contaminated sediment. For green synthesis, extracts of dry leaves of mulberry (ML-nZVI) and oak (OL-nZVI) were used, both abundantly present in the Republic of Serbia. The results show that, despite the fact that their availability was greatly reduced, the metals were concentrated and stabilized to a significant extent in the middle of the EK cell (z/L 0.5) after all treatments. When the results were compared, OL-nZVI proved to be a more effective nanomaterial even with smaller doses of OL-nZVI, which is important in terms of achieving better economic benefits. This study identified green nano zero-valent iron as a powerful tool for metal removal when combined with electrokinetic (EK) treatment, which improves green nZVI longevity and migration. This study of the combined green nZVI-EK remediation treatment, in particular, will have an impact on future research in this field, given the achieved efficiency.

Effect of electrokinetic treatment time on energy consumption and salt ions removal from clayey soils

Electrokinetics effectively removes contaminants, but its field-scale applications are limited mainly due to its high energy cost. In previous studies, the energy consumption was determined either by changing the soil’s specimens initial salt concentration while keeping the treatment time fixed or by changing the treatment time and keeping the same initial salt concentrations for all the specimens. Since both the initial salt concentration and treatment time are important parameters in determining reclamation cost, therefore, in this study, the soil specimens intentionally contaminated with different concentrations of sodium chloride (NaCl), i.e., varying from 3.7 to 15.5 g kg−1, were exposed to a constant DC electric field of 1 V cm−1 for different time durations, i.e., varying from 6 to 72 h. The results show that electroosmotic flow (EOF) was directed from the anode to the cathode and higher for specimens contaminated with relatively low salt concentration, i.e., up to 7.6 g kg−1. Therefore, for these specimens, due to the combined effect of electroosmosis and electromigration, the removal of Na+ was higher than the Cl−. However, for the specimen contaminated with a higher salt concentration, i.e., 15.5 g kg−1, the Cl− removal exceeded Na+ due to the marginalization of EOF. Regardless of initial salt concentration, the electroosmotic flow and salt ions removal rates decreased with increasing treatment time, which might be attributed to the development of acidic and alkaline environments in soil. The collision of acidic and alkaline fronts resulted in a large potential gradient in a narrow soil region of pH jump, diminishing it everywhere else. This nonlinearity in the electric potential distribution in soil reduced the EOF and electromigration of salt ions.