Oxygen vacancies boost the efficacy of MnO2 nanoparticles in catalyzing hydrolytic degradation of organophosphate esters: Implications for managing plastic additive pollution

IF 5.8 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Environmental Science: Nano Pub Date : 2024-11-27 DOI:10.1039/d4en00911h
Zongsheng Liang, keman liu, Yueyue Li, Yaqi Liu, Chuanjia Jiang, Tong Zhang, Wei Chen
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Abstract

The widespread plastic pollution has raised significant concerns. The breakdown process of plastic debris during weathering not only generate microplastics and nanoplastics, but also release large quantities of harmful chemical additives such as phthalates and organophosphate esters (OPEs). Metal oxides, particularly those in the form of nanoparticles, play an essential role in mediating the environmental transformation of plastic additives. However, the key structure–activity relationships governing metal oxide-mediated transformation processes remain poorly understood. Here, we demonstrate that oxygen vacancies (OVs), which are common in metal oxide nanomaterials, significantly contribute to the enhanced catalytic performance of α-MnO2 nanoparticles in promoting the hydrolysis of 4-nitrophenyl phosphate (pNPP), a model OPE pollutant. The α-MnO2 nanorods containing different OV concentrations (obtained by calcination under different atmospheres, i.e., N2 versus air) promote pNPP hydrolysis to different degrees, and the α-MnO2 material with a higher OV concentration shows higher catalytic activity. The results from spectroscopic and theoretical investigations reveal that OVs regulate the adsorption affinity to pNPP by adjusting the coordination saturation of the Mn site on the α-MnO2 surface. Additionally, the enhanced Lewis acidity at these sites (as confirmed by pyridine adsorption infrared spectroscopy and temperature-programmed desorption of ammonia) promotes the electron redistribution in pNPP, which decreases the stability of the P–O bond and enhances the reactivity of α-MnO2 towards pNPP. The findings demonstrate that metal oxide nanomaterials can significantly influence the fate and transformation of microplastic additives, and highlight the potential of defect engineering in amplifying metal oxides’ efficacy for environmental cleanup.
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氧空位提高了二氧化锰纳米颗粒催化水解降解有机磷酸酯的功效:管理塑料添加剂污染的意义
广泛存在的塑料污染引起了人们的极大关注。塑料碎片在风化分解过程中不仅会产生微塑料和纳米塑料,还会释放出大量有害的化学添加剂,如邻苯二甲酸盐和有机磷酸酯(OPEs)。金属氧化物,尤其是纳米颗粒形式的金属氧化物,在塑料添加剂的环境转化过程中发挥着至关重要的作用。然而,人们对金属氧化物介导的转化过程的关键结构-活性关系仍然知之甚少。在这里,我们证明了金属氧化物纳米材料中常见的氧空位(OVs)在促进模型 OPE 污染物--4-硝基苯磷酸酯(pNPP)的水解过程中,能显著提高 α-MnO2 纳米粒子的催化性能。含有不同 OV 浓度的 α-MnO2 纳米棒(通过在不同气氛(即 N2 和空气)下煅烧获得)在不同程度上促进了 pNPP 的水解,OV 浓度较高的α-MnO2 材料显示出较高的催化活性。光谱和理论研究结果表明,OV 通过调节 α-MnO2 表面锰位点的配位饱和度来调节对 pNPP 的吸附亲和力。此外,这些位点上增强的路易斯酸性(经吡啶吸附红外光谱和氨的温度编程解吸证实)促进了 pNPP 中电子的重新分布,从而降低了 P-O 键的稳定性,增强了 α-MnO2 对 pNPP 的反应活性。研究结果表明,金属氧化物纳米材料能显著影响微塑料添加剂的归宿和转化,并突出了缺陷工程在放大金属氧化物环境净化功效方面的潜力。
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来源期刊
Environmental Science: Nano
Environmental Science: Nano CHEMISTRY, MULTIDISCIPLINARY-ENVIRONMENTAL SCIENCES
CiteScore
12.20
自引率
5.50%
发文量
290
审稿时长
2.1 months
期刊介绍: Environmental Science: Nano serves as a comprehensive and high-impact peer-reviewed source of information on the design and demonstration of engineered nanomaterials for environment-based applications. It also covers the interactions between engineered, natural, and incidental nanomaterials with biological and environmental systems. This scope includes, but is not limited to, the following topic areas: Novel nanomaterial-based applications for water, air, soil, food, and energy sustainability Nanomaterial interactions with biological systems and nanotoxicology Environmental fate, reactivity, and transformations of nanoscale materials Nanoscale processes in the environment Sustainable nanotechnology including rational nanomaterial design, life cycle assessment, risk/benefit analysis
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