Characterization and degradation mechanism of bimetallic iron-based/AC activated persulfate for PAHs-contaminated soil remediation

过硫酸盐 双金属片 化学 活性炭 X射线光电子能谱 氧化剂 高分辨率透射电子显微镜 零价铁 核化学 物理吸附 检出限 金属 无机化学 吸附 化学工程 透射电子显微镜 材料科学 催化作用 有机化学 色谱法 纳米技术 工程类
作者
Huifang Tian,Changzhi Chen,Tianle Zhu,Bingjun Zhu,Yifei Sun
出处
期刊:Chemosphere [Elsevier]
卷期号:267: 128875-128875 被引量:24
标识
DOI:10.1016/j.chemosphere.2020.128875
摘要

In this research, a novel iron based bimetallic nanoparticles (Fe–Ni) supported on activated carbon (AC) were synthesized and employed as an activator of persulfate in polycyclic aromatic hydrocarbons (PAHs) polluted sites remediation. AC-supported Fe–Ni activator was prepared according to two-step reduction method: the liquid phase reduction and H2- reduction under high temperature (600 °C), which was defined as Fe–Ni/AC. Characterizations using micropore physisorption analyzer, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and high-resolution transmission electron microscopy (HR-TEM) showed that the synthetic material had large specific surface area, nano-size and carbon-encapsulated metal particles, moreover, the lattice fringes of metals were clearly defined. The PAH compound types and their concentrations were determined by gas chromatography mass spectrometry (GC-MS) with SIM mode, the method detection limit (MDL) was estimated to about 0.21 μg/kg for PAHs, and the average recovery of PAHs was 96.3%. Mechanisms of PAH oxidation degradation with the reaction system of Fe–Ni/AC activated persulfate were discussed, the results showed that short-life free radicals, such as SO4−·, OH·, and OOH· were generated simultaneously, which acted as strong oxidizing radicals, resulting in the oxidation and almost complete opening of the PAH rings.
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