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大气中的微塑料和纳米塑料作为主要空气污染物的载体 - 以聚对苯二甲酸乙二醇酯(PET)为例的理论研究。

Atmospheric microplastics and nanoplastics as vectors of primary air pollutants - A theoretical study on the polyethylene terephthalate (PET) case.

机构信息

Centro Integrativo de Biología y Química Aplicada (CIBQA), Universidad Bernardo O'Higgins, General Gana 1702, Santiago, 8370854, Chile.

Programa Institucional de Fomento a La Investigación, Desarrollo e Innovación, Universidad Tecnológica Metropolitana, Ignacio Valdivieso 2409, San Joaquín, Santiago, 8940577, Chile.

出版信息

Environ Pollut. 2023 Feb 1;318:120860. doi: 10.1016/j.envpol.2022.120860. Epub 2022 Dec 12.

Abstract

Polyethylene terephthalate (PET) microplastics and nanoplastics are ubiquitously present in the atmosphere as atmospheric and airborne forms (PET-aMPs). Using first-principles calculations, we analyze the uptake of primary air pollutants onto PET-aMPs, focusing on their stabilities, adsorption mechanisms, and thermochemistry. The results show that PET-aMPs are selective for the spontaneous adsorption of CO, CO, NO, NO, NO, NH and SO, reaching stable adsorption energies of 6-20 kcal/mol per molecule, with comparable uptake ability than carbon-based materials, metals/metalloids, and metal oxide surfaces. Then, PET-aMPs become a vector for coexisting air pollutants in the atmosphere, which adsorb by inner or outer adsorption depending on the molecular polarity (dipole moment) and atomic constitution (electronegativity) of gaseous molecules. Also, atmospheric HO and O are not competitive molecules, and ozone could enhance adsorption due to surface oxidation and structure breakdown. The interplay of electrostatic (46-61%) and dispersion forces (21-58%) drives the adsorption mechanism, where low-polar pollutants display almost a balanced electrostatic vs. dispersion contribution, while high polar molecules display a higher electrostatic stabilization. The outer adsorption is reached by strong dispersion, hydrogen bonding, and dipole-dipole-induced pairs, while lone-pair-π interactions appear in the inner adsorption regime. These results expand the understanding of the hazards and risks of atmospheric and airborne microplastics/nanoplastics, their impacts, co-transport ability, and interaction with the environment.

摘要

聚对苯二甲酸乙二醇酯(PET)微塑料和纳米塑料作为大气和气载形式(PET-aMPs)普遍存在于大气中。我们使用第一性原理计算分析了大气污染物在 PET-aMPs 上的吸收,重点关注其稳定性、吸附机制和热化学。结果表明,PET-aMPs 对 CO、CO、NO、NO、NO、NH 和 SO 等气体分子的自发吸附具有选择性,达到 6-20 kcal/mol 每个分子的稳定吸附能,与碳基材料、金属/类金属和金属氧化物表面相比,具有相当的吸附能力。然后,PET-aMPs 成为大气中共存空气污染物的载体,根据气体分子的极性(偶极矩)和原子结构(电负性),通过内吸附或外吸附吸附污染物。此外,大气中的 HO 和 O 不是竞争分子,臭氧可以通过表面氧化和结构破坏增强吸附。静电(46-61%)和色散力(21-58%)的相互作用驱动吸附机制,其中低极性污染物的静电与色散贡献几乎平衡,而高极性分子则表现出更高的静电稳定性。外吸附通过强色散、氢键和偶极-偶极诱导对实现,而内吸附则出现孤对-π相互作用。这些结果扩展了对大气和气载微塑料/纳米塑料危害和风险、其影响、共传输能力以及与环境相互作用的理解。

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