Engineering Research Center of Mine Ecological Restoration, Ministry of Education, Xuzhou City, 221116, Jiangsu Province, China.
China University of Mining and Technology, School of Environment and Spatial Informatics, Xuzhou City, 221116, Jiangsu Province, China.
Environ Sci Pollut Res Int. 2023 Dec;30(60):125731-125740. doi: 10.1007/s11356-023-31002-9. Epub 2023 Nov 25.
Biochar-supported nano zero-valent iron (BC@nZVI) is a novel and efficient non-homogeneous activator for persulfate (PS). This study aimed to identify the primary pathways, the degradation mechanism and the performance of phenanthrene (PHE) with PS activated by BC@nZVI (BC@nZVI/PS). BC@nZVI as an activator for PS was prepared by liquid phase reduction method. BC@nZVI was characterized using scanning electron microscopy, transmission electron microscopy, X-ray diffractometer and Fourier transform infrared spectroscopy. The effects of the iron-carbon mass ratio and BC@nZVI dosage were investigated, and a pseudo-first-order kinetic model was used to evaluate the PHE degradation. The results showed that BC supported nZVI and inhibited the agglomeration of nZVI, improving PS's activation efficiency. The optimal iron-carbon mass ratio was determined to be 1:4, accompanied by a dosage of 0.6 g/L of BC@nZVI. During PS activation, nZVI was transformed to Fe and Fe, with the majority being Fe. The reducibility of nZVI in BC@nZVI enabled the reduction of Fe to Fe to activate PS. Radical quenching and electron paramagnetic resonance (EPR) revealed that the oxidative radicals in the BC@nZVI/PS system were mainly SO· and ·OH, where SO· was the primary free radical under acidic and neutral conditions and ·OH in alkaline conditions. Additionally, BC@nZVI adsorption had a limited role in PHE removal. This study can provide mechanism insights of PHE degradation in water with BC@nZVI activation of the NaSO system.
生物炭负载纳米零价铁(BC@nZVI)是一种新型、高效的非均相过硫酸盐(PS)活化剂。本研究旨在确定以 BC@nZVI(BC@nZVI/PS)活化过硫酸盐降解菲(PHE)的主要途径、降解机制和性能。通过液相还原法制备 BC@nZVI 作为 PS 的活化剂。采用扫描电子显微镜、透射电子显微镜、X 射线衍射仪和傅里叶变换红外光谱对 BC@nZVI 进行了表征。考察了铁碳质量比和 BC@nZVI 用量的影响,并采用准一级动力学模型评价了 PHE 的降解。结果表明,BC 负载 nZVI 抑制了 nZVI 的团聚,提高了 PS 的活化效率。最佳铁碳质量比为 1:4,同时 BC@nZVI 的用量为 0.6 g/L。在 PS 活化过程中,nZVI 被转化为 Fe 和 Fe,其中大部分为 Fe。BC@nZVI 中 nZVI 的还原性使 Fe 还原为 Fe 以激活 PS。自由基猝灭和电子顺磁共振(EPR)表明,BC@nZVI/PS 体系中的氧化自由基主要为 SO·和·OH,其中 SO·是酸性和中性条件下的主要自由基,·OH 在碱性条件下。此外,BC@nZVI 吸附对 PHE 的去除作用有限。本研究可为 BC@nZVI 活化 NaSO 体系降解水中 PHE 的机制提供深入了解。