Managed aquifer recharge is an effective strategy for urban stormwater management. Chemical ions are normally retained in stormwater and groundwater and may accelerate clogging during the recharge process. However, the effect of water chemistry on physical clogging has not previously been investigated. In this study, we investigated the hydrogeochemical mechanism of saturated porous media clogging in a series of column experiments. The column was packed with river sand and added suspensions of kaolinite particles. Calcium chloride and sodium chloride are used as representative ions to study chemical effects. We found that an increase in ionic strength resulted in retention of kaolinite solids in the column, with a breakthrough peak of C/C0 value of 1 to 0.2. The corresponding hydraulic conductivity decreased with increased solids clogging. Divalent cations were also found to have a greater influence on kaolinite particle clogging than monovalent cations. The enhanced hydrochemical-related clogging was caused by kaolinite solids flocculating and increasing the deposition rate coefficient by 1 to 2 times in high ionic strength conditions. Three clogging mechanisms of kaolinite solids are proposed: surface filtration, inner blocking, and attachment. This study further deepens the understanding of the mechanisms of solids clogging during aquifer recharge and demonstrates the significance of ionic strength on recharge clogging risk assessments.
Abstract A hydrochemical assessment of the local harvested water and groundwater based on field data, lab experiments, and modeling was carried out for a groundwater artificial recharge (GAR) proposal in the Pinggu Basin aquifer. Harvested water chemically regulated by recharge water standard was chosen as an available recharge source in the basin. The sediments at the potential recharge site were characterized to determine the impact of GAR on subsurface hydrochemistry. To model the dynamic hydrochemical changes during GAR, transport process coupled with the geochemical equilibrium was resolved using PHREEQC and a reverse computing process. These were to simulate chemical reactions, soil soluble species dispersion, mineral dissolution and precipitation, and cation exchange in the recharge vadose zone in the Pinggu Basin. The model was validated by a column leaching experiment and applied for field conditions. The prediction results showed NO 3 − , SO 4 2− , Cl − , and total dissolved solid had peak breakthroughs during the first period of recharge indicating a “washout” phenomenon and then settled down, whilst changes in HCO 3 − , Ca 2+ , Mg 2+ , and pH resulted from carbonate buffering and cation exchange. In the long run, recharge by the harvested water was unlikely to have a negative impact on groundwater quality. Rather caution should be taken for potential chemical clogging induced by dolomite precipitation for a sustainable GAR management.
Hexavalent chromium (Cr(VI)) contamination in groundwater poses a substantial global challenge due to its high toxicity and extensive industrial applications. While the bioelectroremediation of Cr(VI) has attracted huge attention for its eco-friendly attributes, its practical application remains constrained by the hydrogeochemical conditions of groundwater (mainly pH), low electron transfer efficiency, limitations in electrocatalyst synthesis and electrode fabrication. In this study, we developed and investigated the use of N, S co-doped carbon nanofibers (CNFs) integrated on a graphite felt (GF) as a self-standing cathode (NS/CNF-GF) for the comprehensive reduction of Cr(VI) from real contaminated groundwater. The binder free cathode, prepared through electro-polymerization, was employed in a dual-chamber microbial fuel cell (MFC) for the treatment of Cr (VI)-laden real groundwater (40 mg/L) with a pH of 7.4. The electrochemical characterization of the prepared cathode revealed a distinct electroactive surface area, more wettability, facilitating enhanced adsorption and rapid electron transfer, resulting in a commendable Cr(VI) reduction rate of 0.83 mg/L/h. The MFC equipped with NS/CNF-GF demonstrated the lowest charge transfer resistance (Rct) and generated the highest power density (155 ± 0.3 mW/m2) compared to control systems. The favorable electrokinetics for modified cathode led to swift substrate consumption in the anode, releasing more electrons and protons, thereby accelerating Cr(VI) reduction to achieve the highest cathodic coulombic efficiency (C.Eca) of 80 ± 1.3%. A similar temporal trend observed between Cr(VI) removal efficiency, COD removal efficiency, and C.Eca, underscores the effective performance of the modified electrode. The reusability of the binder free cathode, exemption from catholyte preparation and the absence of pH regulation requirements highlighted the potential scalability and applicability of our findings on a larger scale.
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