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MoS 与球磨共修饰污泥生物炭协同作用高效激活过一硫酸盐降解新烟碱类农药:SO、O 和表面结合自由基的主要作用。

MoS coupled with ball milling co-modified sludge biochar to efficiently activate peroxymonosulfate for neonicotinoids degradation: Dominant roles of SO, O and surface-bound radicals.

机构信息

Hubei Key Laboratory of Mineral Resources Processing and Environment, School of Resources and Environmental Engineering, State Key Laboratory of Silicate Materials for Architectures, Wuhan University of Technology, Wuhan, 430070, China.

Hubei Key Laboratory of Mineral Resources Processing and Environment, School of Resources and Environmental Engineering, State Key Laboratory of Silicate Materials for Architectures, Wuhan University of Technology, Wuhan, 430070, China.

出版信息

Environ Res. 2024 Dec 15;263(Pt 1):119983. doi: 10.1016/j.envres.2024.119983. Epub 2024 Sep 12.

Abstract

An efficient catalyst of molybdenum disulfide (MoS) coupled with ball milling modified sludge biochar (BMSBC) was prepared to efficiently activate peroxymonosulfate (PMS) for neonicotinoids elimination. As expected, 95.1% of imidacloprid (IMI) was degraded by PMS/BMSBC system within 60 min and it was accompanied by the outstanding mineralization rate of 71.9%. The superior pore structures, rich defects, oxygen-containing functional groups and grafted MoS on BMSBC offered excellent activation performance for PMS. The influencing factor experiments demonstrated that PMS/BMSBC system performed high anti-interference to wide pH range and background constituents (e.g., inorganic ions and humic acid). Quenching experiments and electron paramagnetic resonance analysis revealed that SO, O, and surface-bound radicals played critical roles in IMI degradation. Electron donors on biochar activated PMS, producing surface radicals. The lone pair electrons within the Lewis basic site of C=O on BMSBC enhanced PMS decomposition by facilitating the cleavage of the -O-O- bond in PMS to release O. The activation process of PMS by MoS accelerated the oxidation of Mo (IV) to Mo (VI) to generate SO. Based on the transformed products (TPs), four degradation pathways of IMI in PMS/BMSBC system were suggested, and all TPs toxicity levels were lower than that of IMI by ECOSAR analysis. Additionally, BMSBC exhibited outstanding sustainable catalytic activity towards PMS activation with the well accepted degradation rate of 71.3% for IMI even after five reuse cycles. PMS/BMSBC system also exhibited satisfactory degradation rates (>71.8%) for IMI in various real waters (e.g., sewage effluent and livestock wastewater). Furthermore, PMS/BMSBC system also offered a favorable broad-spectrum elimination performance for other typical neonicotinoids (e.g., thiamethoxam, clothianidin, thiacloprid) with the degradation rates over 98%. This study has developed a desirable neonicotinoids purification technology in view of its high degradation/mineralization rate, outstanding detoxification performance, satisfied anti-interference to ambient conditions and sustainable sludge management.

摘要

一种高效的二硫化钼(MoS)催化剂与球磨改性污泥生物炭(BMSBC)耦合,用于高效激活过一硫酸盐(PMS)去除新烟碱类杀虫剂。不出所料,PMS/BMSBC 体系在 60 分钟内可降解 95.1%的吡虫啉(IMI),同时具有 71.9%的出色矿化率。BMSBC 具有优异的孔结构、丰富的缺陷、含氧官能团和接枝 MoS,为 PMS 的高效激活提供了优异的性能。影响因素实验表明,PMS/BMSBC 体系对宽 pH 范围和背景成分(如无机离子和腐殖酸)具有高抗干扰性。淬灭实验和电子顺磁共振分析表明,SO、O 和表面结合自由基在 IMI 降解中起着关键作用。生物炭上的电子供体激活了 PMS,产生了表面自由基。BMSBC 上 C=O 中路易斯碱性位的孤对电子通过促进 PMS 中-O-O-键的断裂来释放 O,从而增强了 PMS 的分解。MoS 对 PMS 的活化过程加速了 Mo(IV)向 Mo(VI)的氧化,从而生成 SO。基于转化产物(TPs),提出了 PMS/BMSBC 体系中 IMI 的四种降解途径,并且所有 TPs 的毒性水平都低于 ECOSAR 分析的 IMI。此外,BMSBC 对 PMS 活化具有出色的可持续催化活性,即使在五次重复使用后,IMI 的降解率仍保持在 71.3%。PMS/BMSBC 体系对各种实际水样(如污水和牲畜废水)中的 IMI 也表现出令人满意的降解率(>71.8%)。此外,PMS/BMSBC 体系对其他典型新烟碱类杀虫剂(如噻虫嗪、噻虫胺、噻虫啉)也具有良好的广谱去除性能,降解率均超过 98%。鉴于其高降解/矿化率、出色的解毒性能、对环境条件的良好抗干扰性和可持续的污泥管理,本研究为新烟碱类杀虫剂的净化技术提供了一种理想的选择。

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