Soil contamination due to chlorinated organics prompts an important environmental problem; however, the iron-based reduction materials and complicated ground environment are the main barriers to implementation and promotion of in situ soil remediation. Therefore, this study aims to evaluate the reductants zero-valent iron (ZVI) and its activated carbon composite (AC-ZVI) in terms of their self-oxidation and selectivity in soil experiments. The results indicated that saturated moisture conditions were beneficial for degradation due to the dispersal of the pollutants from soil particles. Particularly, increasing the water/soil ratio to the over-saturated state would decrease the selectivity of ZVI and AC-ZVI. Meanwhile, increasing the reductant loading decreased the selectivity of ZVI and AC-ZVI, whereas the high initial concentration increased the selectivity of AC-ZVI. In addition, the self-oxidation of ZVI (3.0 ×10 h) is 4.2 times higher than that of AC-ZVI (0.7 ×10 h), and the selectivity of AC-ZVI (48%) is 6.9 times higher than that of ZVI (7%), which confirmed that AC-ZVI is a superior iron-based amendment in saturated moisture conditions. Therefore, this study provides a reliable and feasible evaluation method for in situ remediation process, and deepens the understanding of the effects of moisture contents.
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http://dx.doi.org/10.1016/j.jhazmat.2021.127322 | DOI Listing |
Small
October 2024
College of Materials Science and Engineering, Sichuan University, Chengdu, 610064, P. R. China.
J Hazard Mater
September 2024
School of Environment Science and Engineering, Donghua University, Shanghai 201620, PR China; Shanghai Institution of Pollution Control and Ecological Security, Shanghai 200092, PR China; State Environmental Protection Engineering Center for Pollution Treatment and Control in Textile Industry, Donghua University, Shanghai 201620, PR China. Electronic address:
Charged natural chalcopyrite (CuFeS, Ncpy) was developed for a three-dimensional electrochemical nitrate reduction (3D ENORR) system with carbon fiber cloth cathode and Ti/IrO anode and Zn-NO battery. The 3D ENORR system with Ncpy particle electrodes (PEs) possessed superior nitrate removal of 95.6 % and N selectivity of 76 % with excellent reusability under a broad pH range of 2-13 involving heterogeneous and homogeneous radical mechanisms.
View Article and Find Full Text PDFAdv Sci (Weinh)
July 2024
Graduate School of Pharmaceutical Sciences, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan.
Angew Chem Int Ed Engl
June 2024
State Key Laboratory of Low Carbon Catalysis and Carbon Dioxide Utilization, State Key Laboratory for Oxo Synthesis and Selective Oxidation, Lanzhou Institute of Chemical Physics (LICP), Chinese Academy of Sciences, Lanzhou, 730000, China.
Electrocatalytic carbonylation of CO and CHOH to dimethyl carbonate (DMC) on metallic palladium (Pd) electrode offers a promising strategy for C1 valorization at the anode. However, its broader application is limited by the high working potential and the low DMC selectivity accompanied with severe methanol self-oxidation. Herein, our theoretical analysis of the intermediate adsorption interactions on both Pd and Pd surfaces revealed that inevitable reconstruction of Pd surface under strongly oxidative potential diminishes its CO adsorption capacity, thus damaging the DMC formation.
View Article and Find Full Text PDFNat Commun
March 2024
State Key Laboratory of Chem/Bio-Sensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha, 410000, P. R. China.
Preventing the deactivation of noble metal-based catalysts due to self-oxidation and poisonous adsorption is a significant challenge in organic electro-oxidation. In this study, we employ a pulsed potential electrolysis strategy for the selective electrocatalytic oxidation of glycerol to glyceric acid over a Pt-based catalyst. In situ Fourier-transform infrared spectroscopy, quasi-in situ X-ray photoelectron spectroscopy, and finite element simulations reveal that the pulsed potential could tailor the catalyst's oxidation and surface micro-environment.
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