This article presents a perspective on the current reclaimed water quality standards for clogging control during aquifer storage and recovery (ASR) in China. Water reuse and ASR in China are reviewed, and we examine how clogging contributes to the failures of ASR. We identify loopholes in current standards for clogging control. The threshold values of suspended solids and turbidity in these standards are effective for the prevention of clogging triggered by inorganic mineral suspended particles in regular recharge water sources (e.g., rainfall and floodwater). However, these threshold values are not low enough to prevent clogging when secondary effluent from wastewater treatment plants containing organic flocs of active sludge is introduced. Therefore, revision of current standards for clogging control is urgently needed.
Artificial recharge engineering has been widely used to solve the water resource crisis. However, there are still some safety hazards regarding reclaimed water quality. Here, chlorinated secondary effluent (SE) was injected into saturated porous media composed of high–purity quartz sands. The column experiment was conducted and modeled through a developed numerical model to predict the evolution of physical clogging. Some representative inorganic and organic indicators were measured both at different times and in different column sections. The study showed that the relative hydraulic conductivity (K/K0) decreased significantly by approximately 63.5% in 40 h. Especially for the first 3 cm of the column, the clogging was the most serious, with a decrease of approximately 85.8%. The porous media has a certain degree of filtration effect on turbidity, TOC, protein (Pr) and polysaccharide (PS) but has slight removal for other water quality indicators. Pr is the main component of the intercepted TOC, and its content is higher than that of Ps. Moreover, the inorganic and organic parameter variations along the column further verified that the organic floc particles were mainly retained in the first 3 cm. The 3D excitation/emission matrix (3DEEM) fluorescence spectra illustrated that the humic acids and fulvic acids were easy to release and that their injection may be harmful to groundwater quality. The study will lay a theoretical foundation and provide a guiding scheme for optimizing China’s reclaimed water reuse technology, ensuring the safety of reclaimed water quality.
With increasing awareness of reduction of energy and CO2 footprint, more waste is considered recyclable for generating value-added products. Here we reported the negatively-valued iron mud, a waste from groundwater treatment plant, was successfully converted into magnetic adsorbent. Comparing with the conventional calcination method under the high temperature and pressure, the synthesis of the magnetic particles (MPs) by Fe2+/Fe3+ coprecipitation was conducted at environment-friendly condition using ascorbic acid (H2A) as reduction reagent and nitric acid (or acid wastewater) as leaching solution. The MPs with major component of Fe3O4 were synthesized at the molar ratio (called ratio subsequently) of H2A to Fe3+ of iron mud ≥ 0.1; while amorphous ferrihydrite phase was formed at the ratio ≤ 0.05, which were confirmed by vibrating sample magnetometer (VSM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). With the ratio increased, the crystalline size and the crystallization degree of MPs increased, and thus the Brunauer-Emmett-Teller (BET) surface and the cation-exchange capacity (CEC) decreased. MPs-3 prepared with H2A to Fe3+ ratio of 0.1 demonstrated the highest methylene blue (MB) adsorption of 87.3 mg/g and good magnetic response. The adsorption of MB onto MPs agreed well with the non-linear Langmuir isotherm model and the pseudo-second-order model. Pilot-scale experiment showed that 99% of MB was removed by adding 10 g/L of MPs-3. After five adsorption-desorption cycles, MPs-3 still showed 62% removal efficiency for MB adsorption. When nitric acid was replaced by acid wastewater from a propylene plant, the synthesized MPs-3w showed 3.7 emu/g of saturation magnetization (Ms) and 56.7 mg/g of MB adsorption capacity, 2.8 times of the widely used commercial adsorbent of granular active carbon (GAC). The major mechanism of MPs adsorption for MB was electrostatic attraction and cation exchange. This study synthesized a magnetic adsorbent from the negatively-valued iron mud waste by using an environment-friendly coprecipitation method, which had a potential for treatment of dye wastewater.
Despite recent advancements in photocatalysis enabled by materials science innovations, the application of photocatalysts in water treatment is still hampered due to low overall efficiency. Herein, we present a TiO2 photocatalytic process with significantly enhanced efficiency by the introduction of micro–nano bubbles (MNBs). Notably, the removal rate of a model organic contaminant (methylene blue, MB) in an air MNB-assisted photocatalytic degradation (PCD) process was 41–141% higher than that obtained in conventional macrobubble (MaB)-assisted PCD under identical conditions. Experimental observations and supporting mechanistic modeling suggest that the enhanced photocatalytic degradation is attributed to the combined effects of increased dissolution of oxygen, improved colloidal stability and dispersion of the TiO2 nanocatalysts, and interfacial photoelectric effects of TiO2/MNB suspensions. The maximum dissolved oxygen (DO) concentration of the MNB suspension (i.e., 11.7 mg/L) was 32% higher than that of an MaB-aerated aqueous solution (i.e., 8.8 mg/L), thus accelerating the hole oxidation of H2O on TiO2. We further confirmed that the MNBs induced unique light-scattering effects, consequently increasing the optical path length in the TiO2/MNB suspension by 7.6%. A force balance model confirmed that a three-phase contact was formed on the surface of the bubble–TiO2 complex, which promoted high complex stability and PCD performance. Overall, this study demonstrates the enhanced photocatalytic water decontamination by MNBs and provides the underlying mechanisms for the process.
When reclaimed water was recharged into groundwater containing a low content of ferrous iron, Fe-rich particles were generated and started to transport into the porous medium. X-ray powder diffraction and Mössbauer spectroscopy analysis showed that the generated Fe-rich particles were in a poorly crystallized ferrihydrite phase. After the formation of ferrihydrite particles, the mass loss of contaminants was calculated, which was 88.2% for Al, 93.3% for Zn, and 41.6% for chemical oxygen demand (COD). Protein-like compounds were predominant in the removed COD. Bovine serum albumin (BSA) was used as a model to investigate the effect of proteins on the transport of ferrihydrite particles in porous medium. Results showed that the attachment efficiency of ferrihydrite particles on the porous medium decreased from 100% to 75% with the increase of BSA concentration from 10 mg/L to 100 mg/L. BSA was attached to the surface of ferrihydrite particles via electrostatic adsorption. Thus, the zeta potential of ferrihydrite particles changed from positive to negative, and the particles became less aggregated, thereby enhancing particle mobility. This observation provided evidence that protein residues in reclaimed water enhance the transport of Fe-rich particles in saturated porous medium.
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