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Manganese oxide-activated persulfate plays a critical role in water purification and in situ chemical oxidation processes, but the underlying mechanism needs to be further revealed. Herein, the detailed mechanism of MnO

Neonicotinoids pose potential serious risks to human health even at environmental concentration and their removal from water is considered as a great challenge. A novel ball milling and acetic acid co-modified sludge biochar (BASBC) was the first time synthesized, which performed superior physicochemical characteristics including larger surface area, more defect structures and functional groups (e.g., CO and -OH). Electrochemistry was introduced to enhance BASBC for peroxymonosulfate (PMS) activation (E/BASBC/PMS) to degrade environmental concentration neonicotinoids (e.g., imidacloprid (IMI)). The degradation efficiency of IMI was 95.2% within 60 min (C

In this study, a novel heterogeneous ultrasonic (US)-enhanced sludge biochar (SBC) activated periodate (PI) system was established and explored for the rapid removal of levofloxacin in the aqueous environment. This study focused on the mechanisms of US-enhanced SBC co-activation of PI for levofloxacin degradation. The results indicated that US and SBC exhibited a remarkable synergistic reinforcing activation effect on PI compared to single PI activation systems. The SBC/US/PI system achieved approximately 95% of levofloxacin removal, 51.5% of TOC removal, and 22% of dechlorination rate within 60 min with virtually no heavy metals released into the water matrix. In addition, the acute ecotoxicity of the solutions treated with the SBC/US/PI system was substantially reduced. The presence of IO

Environmental concentration imidacloprid (IMI) has become a potential risk to ecological safety and human health, therefore an efficient, sustainable and environment friendly approach was urgently needed for its removal. In this study, a novel graphene oxide supported magnetic sludge biochar composite (GO/CoFe2O4-SBC) was first time synthesized and assessed for IMI removal at environmental concentration level. The maximum adsorption capacity of GO/CoFe2O4-SBC for IMI was 8.64 × 103 μg g−1. Physicochemical characteristics, kinetics (pseudo-second-order), isotherms (Freundlich and Temkin), thermodynamics and environmental factors analysis suggested that its outstanding adsorption performance was mainly attributed to pore filling, π-π conjugation and functional groups interaction. The mechanisms analysis indicated that intraparticle diffusion was the main rate-limiting step and its adsorption was a spontaneous, endothermic and randomness increased process. The magnetic sensitivity enabled it to be easily separated from water. The sustainable adsorption capacity (>90% of the initial adsorption capacity) of GO/CoFe2O4-SBC was well maintained by ethanol extraction even after five reuse cycles. GO/CoFe2O4-SBC also exhibited environmental security with its leaching concentrations of Fe and Co were below 0.5 mg L−1 in a wide pH range. The performance of GO/CoFe2O4-SBC suggested that it could be served as a promising adsorbent for environmental concentration IMI removal.

Perfluorooctanoic acid (PFOA) and perfluorooctane sulfonic acid (PFOS) have attracted global attention due to their chemical durability, wide distribution, biotoxicity and bioaccumulative properties. Persulfate is a promising alternative to H2O2 for advanced oxidation processes and effective for organic removal. In this review, persulfate activation methods and operational factors in persulfate-based PFOA / PFOS degradation are analyzed and summarized. Moreover, the decomposing mechanisms of PFOA and PFOS are outlined in terms of molecular structures based a series of proposed pathways. PFOS could be converted to PFOA with the attack of SO4- and OH. And then PFOA defluorination occurs with one CF2 unit missing in each round and the similar procedure would occur continuously with sufficient SO4- and OH until entire decomposition. In addition, several knowledge gaps and research needs for further in-depth studies are identified. This review provides an overview for better understanding of the mechanisms and prospects in persulfate-based degradation of PFOA and PFOS.

Municipal solid waste (MSW) leachate contains various refractory pollutants that pose potential threats to both surface water and groundwater. This paper established a novel catalytic oxidation process for leachate treatment, in which OH is generated in situ by pumping both H2 and O2 in the presence of Pd catalyst and Fe2+. Volatile fatty acids in the leachate were removed almost completely by aeration and/or mechanical mixing. In this approach, a maximum COD removal of 56.7% can be achieved after 4 h when 200 mg/L Fe2+ and 1250 mg/L Pd/Al2O3 (pH 3.0) are used as catalysts. After oxidation, the BOD/COD ratio in the proposed process increased from 0.03 to 0.25, indicating that the biodegradability of the leachate was improved. By comparing the efficiency on COD removal and economical aspect of the proposed Pd-based in-situ process with traditional Fenton, electro-Fenton and UV-Fenton for leachate treatments, the proposed Pd-based in-situ process has potential economic advantages over other advanced oxidation processes while the COD removal efficiency was maintained.