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FeMgAl−MoS4 LDH was successfully synthesized by a one-pot hydrothermal process followed by ion-exchange methods, and this novel adsorbent was first conducted for aqueous selenite and selenate elimination. The Fe as a component for metal cation layers of LDHs could modulate the layer charge density, leading to more functional groups inserted into layers, and more importantly, this heterogeneous Fe can catalyze the surface reactions between Se(IV) or Se(VI) with S(-II) for oxoanions sequestration. The mechanisms are ion exchange between functional groups with HSeO3− and SeO32− for Se(IV) or SeO42− for Se(VI), followed by reduction by S(-II) from MoS42− groups. The existence of Fe in LDH cation layers, obviously enhanced the reactions (almost two times more for Se(IV) and three times more for Se(VI), respectively), resulting in satisfying adsorption capacities of 483.9 mg/g and 167.2 mg/g for Se(IV) and Se(VI), respectively. Mechanisms were further revealed by elementary analysis, XRD, FT−IR, SEM−EDX, and XPS, as well as the quantitative study. For sorption kinetics, the calculated values of capacities from the pseudo-second-order model are much closer to the experimental values. For sorption isotherms, Langmuir is better than the Freundlich isotherms model for closer capacities (505 mg/g for selenite and 172 mg/g for selenate). All these results demonstrated that the presence of heterogeneous Fe could catalyze the reduction of Se (IV/VI) for the aqueous system, and maybe other high oxidative states hazardous ions. So FeMgAl−MoS4 is a kind of novel adsorbent that offers a promising multi-functional and highly efficient solution for water selenium purification. [ABSTRACT FROM AUTHOR]

Pyrolysis under protective atmosphere was regarded as an indispensable process for the preparation of biomass-based adsorbents to achieve higher surface areas. In this paper, magnetic carbon composites (MCC) that fabricated under air atmosphere showed an adsorption capacity of 167.22 mg/g in 200 ppm Hg(II), which was significantly higher than magnetic biochar (MBC, 31.80 mg/g) that fabricated under traditional nitrogen protection, and this remarkable performance of MCC was consistent in a wide range of pHs. Based on BET, XRD, FTIR, SEM and Boehm titration, MCC was demonstrated with limited surface area (43.29 m 2 /g) but large amount of surface functional groups comparing with MBC. Additionally, γ-Fe 2 O 3 with a high degree of crystallization was generated in MCC, which led to a better magnetic property and recyclability. Moreover, characterizations, Langmuir isotherm and pseudo-second-order kinetics demonstrated the chemisorption was dominant for MCC in mercury capture, and surface complexation co-precipitate of Hg 4 Fe 8 O 16 C 56 H 40 were also formed. [ABSTRACT FROM AUTHOR]

A novel strategy for the removal of refractory organic contaminants was realized through sludge-derived biochar (SDBC)/persulfate (PS) system via both adsorption and advanced oxidation process under ambient conditions. SDBC was prepared by one single step of slow pyrolysis of municipal sewage sludge, appeared a porous structure, and contained abundant oxygen-containing functional groups as well as amorphous Fe species. Large surface area and porous structure of SDBC benefitted the adsorption and enrichment of contaminants, while oxygen-containing functional groups and Fe species on the surface were considered as reactive components for the activation of PS. Under conditions of [PS] 0 = 1.85 mM, [4-chlorophenol] 0 = 0.039 mM, [SDBC] 0 = 1 g L −1 , pH 0 = 6.30 and temperature = 25 °C, the removal of model compound of 4-chlorophenol achieved 92.3%, and this significant performance of SDBC/PS system was consistent in a broad pH window. Radical scavengers and electron paramagnetic resonance (EPR) studies suggested that SDBC successfully activated PS to produce various oxidative radicals. Meanwhile, recycle experiments and Fe 3+ leaching tests further demonstrated the stability of SDBC during the activation of PS. Municipal landfill leachate effluent through a membrane bio-reactor was testified as the refractory real wastewater, in which both the removal of total organic carbon and ammonia was significant. Thus, SDBC showed certain advantages in PS activation such as feasible preparation method, remarkable efficiency and stability. These advantages proved SDBC/PS system as an effective strategy of controlling waste by waste, and implicated its potential application in full-scale for the treatment of refractory organic contaminants. [ABSTRACT FROM AUTHOR]