Surface-Confined Anchoring of Highly Dispersed Nanocobalt Promotes Advanced Oxidation for Eliminating Health-Threatening Organics

IF 4.7 2区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR Inorganic Chemistry Pub Date : 2025-03-19 DOI:10.1021/acs.inorgchem.5c00611
Haijian Wang, Yicheng Zhang, Xinyue Cui, Xiqian Cao, Yang Su, Mengshan Chen, Jinghu Wang, Xue Zhao, Yingtang Zhou
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Abstract

Peroxymonosulfate (PMS)-based advanced oxidation processes are effective in eliminating health-threatening persistent organic pollutants (POPs), but they require the participation of high-performance catalysts. In this study, a highly dispersed nanocobalt species (Co-NHCSs) was constructed on nitrogen-doped hollow carbon spheres by using the double confinement mechanism of complexation confinement combined with spatial confinement. The Co-NHCSs/PMS system has a high degradation efficiency of 95.2% for tetracycline within 30 min, and the degradation performance was almost not attenuated after repeated use 10 times. The Co-NHCSs/PMS system can also resist the interference of a complex water environment to achieve efficient degradation of POPs in multiple scenarios. Reactive oxygen quenching experiments and electron paramagnetic resonance confirmed that Co-NHCSs promoted the activation of PMS into ·OH, SO4·–, and 1O2 with high oxidation potential, which promoted the degradation of POPs. Density functional theory calculations show that nano-Co anchored on NHCSs can spontaneously capture and activate PMS on either a planar carbon matrix or a curved carbon matrix, which is the key to the efficient degradation of POPs by the Co-NHCSs/PMS system. This study not only provides an innovative way to construct nanometal catalysts but also reveals the transformation behavior of PMS on cobalt-based materials, which is of great significance for promoting PMS-based wastewater treatment technology.

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高度分散的纳米钴的表面限制锚定促进高级氧化,以消除对健康有害的有机物
以过氧单硫酸盐(PMS)为基础的高级氧化工艺可以有效地去除危害健康的持久性有机污染物(POPs),但它需要高性能催化剂的参与。本研究利用络合约束与空间约束相结合的双重约束机制,在氮掺杂的空心碳球上构建了高度分散的纳米钴(Co-NHCSs)。Co-NHCSs/PMS体系在30 min内对四环素的降解效率高达95.2%,重复使用10次后降解性能几乎不衰减。Co-NHCSs/PMS系统还可以抵抗复杂水环境的干扰,在多种情况下实现持久性有机污染物的有效降解。活性氧猝灭实验和电子顺磁共振实验证实,co - nhcs促进PMS活化成高氧化电位的·OH、SO4·-和1O2,促进了POPs的降解。密度泛函理论计算表明,锚定在nhcs上的纳米co可以在平面或弯曲碳基体上自发捕获并激活PMS,这是co - nhcs /PMS体系高效降解持久性有机污染物的关键。本研究不仅为构建纳米金属催化剂提供了创新途径,而且揭示了PMS在钴基材料上的转化行为,对推广PMS基废水处理技术具有重要意义。
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来源期刊
Inorganic Chemistry
Inorganic Chemistry 化学-无机化学与核化学
CiteScore
7.60
自引率
13.00%
发文量
1960
审稿时长
1.9 months
期刊介绍: Inorganic Chemistry publishes fundamental studies in all phases of inorganic chemistry. Coverage includes experimental and theoretical reports on quantitative studies of structure and thermodynamics, kinetics, mechanisms of inorganic reactions, bioinorganic chemistry, and relevant aspects of organometallic chemistry, solid-state phenomena, and chemical bonding theory. Emphasis is placed on the synthesis, structure, thermodynamics, reactivity, spectroscopy, and bonding properties of significant new and known compounds.
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