Publications by authors named "Zongsu Wei"

Hydrated electrons (e; ‒2.9 V) are effective at defluorinating per- and polyfluoroalkyl substances (PFAS), but production of e often requires excess source chemicals, anoxic environment, and harsh pH conditions. To improve the feasibility of the reductive process, we harnessed phenol as a source chemical yielding four e stoichiometrically and utilized dithionite (DTN) to catalyze phenol cycle for sustained e yields.

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Rare earth elements (REEs) are the "fuel" for high-tech industry, yet their selective recovery from complex waste matrices is challenging. Herein, we designed a 2D multilayered MXene TiCT adsorbent for selective extraction of REEs in a broad pH range. By establishing strong Lewis acid-base interactions, extraction capacities of TiCT to Eu(III) and Ho(III) reached 892.

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In landfill leachates containing complex dissolved organic matter (DOM), the link between individual DOM constituents and their inherent oxidizability is unclear. Here, we resolved the molecular signatures of DOM oxidized by OH/O using FT-ICR MS, thereby elucidating their oxidizability and resistance in concentrated leachates. The comprehensive gradual fragmentation of complex leachate DOM was then revealed through a modified machine-learning framework based on 43 key pathways during ozonation.

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Per- and polyfluoroalkyl substances (PFAS) with stable carbon-fluorine bonds are used in a wide range of industrial and commercial applications. Due to their extreme environmental persistence, PFAS have the potential to bioaccumulate, cause adverse effects, and present challenges regarding remediation. Recently, microbial and enzymatic reactions for sustainable degradation of PFAS have gained attention from researchers, although biological decomposition of PFAS remains challenging.

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UV/peroxydisulfate (UV/PDS) process is known to be highly efficient for degrading micropollutants from water by generating sulfate (SO) and hydroxyl radicals (HO). Reliable analyses of short-lived SO and HO are therefore critical for understanding reaction mechanisms and optimizing operating conditions. Currently, alcohols are commonly used as quenchers to distinguish radicals based on the assumption that they exclusively react with target radicals without other influences.

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Visible light photocatalysis is widely considered a sustainable approach to break down micropollutants without chemical addition. To promote the output of photogenerated carriers under visible light, a Z-scheme plasmonic photocatalyst Bi-CeO/Ag/BiO was designed and fabricated to activate dissolved oxygen in water for micropollutant degradation. The doped Bi not only improved the separation of electron-hole, but also narrowed the band gap of CeO to enhance its absorption of visible light.

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Perfluorooctanoic acid (PFOA) is a toxic and recalcitrant perfluoroalkyl substance commonly detected in the environment. Its low concentration challenges the development of effective degradation techniques, which demands intensive chemical and energy consumption. The recent stringent health advisories and the upgrowth and advances in photocatalytic technologies claim the need to evaluate and compare the state-of-the-art.

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Given that the spontaneous precipitation of minerals caused by urea hydrolysis and abundant organic compounds, membrane fouling became a major obstacle for urine recovery by membrane distillation (MD). Herein, this study developed a combined system (TAP-MD) by integrating thermally activated peroxydisulfate (TAP) and MD process to inhibit membrane fouling and improve separation efficiency. Based on the TAP-MD system, the separation performance was improved significantly, improving nutrient recovery efficiency and quality of reclaimed water.

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Urbanization and industrialization have exerted significant adverse effects on water quality, resulting in a growing need for reliable and eco-friendly treatment technologies. Persulfate (PS)-based advanced oxidation processes (AOPs) are emerging as viable technologies to treat challenging industrial wastewaters or remediate groundwater impacted by hazardous wastes. While the generated reactive species can degrade a variety of priority organic contaminants through radical and nonradical pathways, there is a lack of systematic and in-depth comparison of these pathways for practical implementation in different treatment scenarios.

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Photochemical transformation is an important process that involves trace organic contaminants (TrOCs) in sunlit surface waters. However, the environmental implications of their self-photosensitization pathway have been largely overlooked. Here, we selected 1-nitronaphthalene (1NN), a representative nitrated polycyclic aromatic hydrocarbon, to study the self-photosensitization process.

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In this study, SiO-composited biochar decorated with Fe/Mn was prepared by co-pyrolysis method. The degradation performance of the catalyst was evaluated by activating persulfate (PS) to degrade tetracycline (TC). The effects of pH, initial TC concentration, PS concentration, catalyst dosage and coexisting anions on degradation efficiency and kinetics of TC were investigated.

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Advanced oxidation/reduction of PFAS is challenged and concerned by the formation of toxic, short-chain intermediates during water treatments. In this study, we investigated the complete defluorination of PFOA by ultrasound/persulfate (US/PS) with harmless end-products of CO, HO, and F ions. We observed 100% defluorination after 4 h of US treatment alone with a power input of 900 W.

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Electro-Fenton (EF) process represents an energy-efficient and scalable advanced oxidation technology (AOT) for micropollutants removal in wastewaters. However, mechanistic profiling and quantitation of contribution of each subprocess (i.e.

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Hydroxylamine (NHOH), nitrite (NO) and nitric oxide (NO), intermediates enzymatically formed during biological nitrogen removal processes, can engage in chemical (abiotic) transformations of antibiotics. This study determined the kinetics, mechanisms and pathways of abiotic transformations of the antibiotic sulfamethoxazole (SMX) by NHOH, NO and NO in a series of batch tests under different pH and oxygen conditions. While NHOH was not able to directly transform SMX, NO (with HNO as the actual reactant) and NO can chemically transform SMX primarily through hydroxylation, nitration, deamination, nitrosation, cleavage of S-N, N-C and C-S bonds, and coupling reactions.

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"Concentrate-and-degrade" is an effective strategy to promote mass transfer and degradation of pollutants in photocatalytic systems, yet suitable and cost-effective photocatalysts are required to practice the new concept. In this study, we doped a post-transition metal of Indium (In) on a novel composite adsorptive photocatalyst, activated carbon-supported titanate nanotubes (TNTs@AC), to effectively degrade perfluorooctanoic acid (PFOA). In/TNTs@AC exhibited both excellent PFOA adsorption (>99% in 30 min) and photodegradation (>99% in 4 h) under optimal conditions (25 °C, pH 7, 1 atm, 1 g/L catalyst, 0.

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This study reported the reactivity and mechanisms of superoxide radical (O˙)-mediated transformation of pentachlorophenate. Our results indicated that O˙ alone exhibits limited effects on its degradation, and bimolecular nucleophilic substitution is the dominant reaction pathway.

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Perfluorocarboxylic acids (PFCAs) exhibit strong persistence in sunlit surface waters and in radical-based treatment processes, where superoxide radical (O) is an important and abundant reactive oxygen species. Given that the role of O during the transformation of PFCAs remains largely unknown, we investigated the kinetics and mechanisms of O-mediated PFCAs attenuation through complementary experimental and theoretical approaches. The aqueous-phase rate constants between O and C3-C8 PFCAs were measured using a newly designed spectroscopic system.

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In the application of various magnetic materials for water treatment, control of surface resistance to acid and alkali corrosion remains largely overlooked, which could greatly extend their service life. We herein prepare amino grafted magnetic graphene oxide composites using a simple one-step cross-link reaction between the graphene oxide and magnetic FeO/C nanoparticles. The as-prepared magnetic graphene oxide composites have long-term stability under acid and alkali solutions and shows an excellent performance in removing Ho(III), a representative rare earth element (REE) from water.

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Pressurized vertical electro-osmotic dewatering (PVEOD) has been regarded as a feasible method to achieve sludge deep-dewatering, but the dewatering efficiency is still challenged by high electric resistance. This study employed cationic polyacrylamide (CPAM) as a skeleton builder to enhance electro-osmotic flow in PVEOD. The sludge dewatering efficiency and synergistic effect of CPAM and PVEOD were elucidated.

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The adsorbents with high adsorption capacity for simultaneously removing Cr(VI) and Hg(II) from aqueous solutions under broad working pH range are highly desirable but still extremely scarce. Here, a novel adsorbent with multidentate ligands was facilely fabricated by covalently bonding 4-amino-3-hydrazino-5-mercapto- 1,2,4-triazole on graphene oxide via the Schiff's base reaction. The maximum adsorption capacities of Cr(VI) and Hg(II) on the current adsorbent were 734.

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Microbially induced carbonate precipitation (MICP) could be a potential green solution to resolve the issue of heavy metal releasing from the sulfide tailings. However, detailed mechanism of heavy metal-biomineralization in sulfide tailings and impact of procedure parameters on in-situ applications remain unexplored. We systematically investigated the biomineralization process in the column tests for a better understanding of the mechanism and effects on the inhibition of cadmium (Cd) releasing from sulfide tailings.

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Mass transfer efficiency and catalytic reactivity are the two major hurdles for heterogeneous catalytic wet peroxide oxidation (CWPO) technologies. To address these issues, nanocomposite CuFeO/AlO was synthesized and assessed as a novel catalyst for enhanced adsorption and oxidation of anionic pollutants (catechol and reactive red 195 (RR195)) in waters. With a positive charge on the nanocomposite by introducing AlO, the adsorption of anionic pollutants was promoted.

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The production of fine particles from extremely high supersaturation has challenged the application of sulfide precipitation in treating heavy metal wastewater due to the difficulty of solid-liquid separation. To this end, a gas-liquid sulfide precipitation reactor for the removal of Cu was designed by controlling the mass transfer and supersaturation levels during sulfidation processes. Particularly, a computational fluid dynamics (CFD) model of the reactor, integrating sulfidation reaction kinetics with two-phase flow hydrodynamics, was first built, followed by examining the effects of HS(g) bubble diameter and flow rate.

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Interests in the kinetics of radical-induced reactions in aqueous solution have grown remarkably due to their water engineering significance (e.g., advanced oxidation processes).

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