聚苯乙烯微塑料在三种不同过滤介质中迁移行为的比较研究:石英砂、沸石和无烟煤

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-07-01 DOI:10.1016/j.jconhyd.2024.104395
Haicheng Liu, Yu Wen, Jingkun Xu
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引用次数: 0

摘要

微塑料(MPs)是一种新出现的污染物,正引起研究人员越来越多的关注,其在过滤过程中的迁移对饮用水的安全影响很大。研究选取了聚苯乙烯(PS)作为代表性的微塑料,并使用了水厂中常见的三种过滤介质(石英砂、沸石和无烟煤)。借助 DLVO 理论和胶体过滤理论,对各种过滤介质在不同背景水质条件下截留 PS-MPs 的模式进行了系统研究。结果表明,三种过滤介质的不同结构和元素组成导致它们表现出不同的表面粗糙度和表面电位。与石英砂相比,沸石和无烟煤的表面粗糙度越大,其抑制 PS-MPs 迁移的能力就越强。然而,表面粗糙度并不是影响 MPs 迁移的唯一因素。无烟煤表面电位的绝对值较低,导致无烟煤与 PS-MPs 之间的 DLVO 能量明显低于沸石与 PS-MPs 之间的 DLVO 能量,从而导致表面粗糙度较低的无烟煤比表面粗糙度较高的沸石更能留住 PS-MPs。PS-MPs 在介质中的迁移受到过滤介质表面粗糙度和 DLVO 能量的共同影响。在相同的操作条件下,三种过滤材料对 PS-MPs 的截留效率依次为石英砂、沸石和无烟煤。此外,溶液条件对 PS-MPs 在模拟滤柱中的迁移能力也有明显影响。随着溶液离子强度和阳离子价数的增加,PS-MPs 在模拟滤柱中的迁移量减少。当然,溶解的有机物会促进 PS-MPs 在滤层中的迁移,而腐植酸的促进作用要比富勒酸大得多。研究结果可能有助于提高过滤单元截留 MPs 的能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Comparative study of polystyrene microplastic transport behavior in three different filter media: Quartz sand, zeolite, and anthracite

Microplastics (MPs) are emerging contaminants that are attracting increasing interest from researchers, and the safety of drinking water is greatly affected by their transportation during filtration. Polystyrene (PS) was selected as a representative MPs, and three filter media (quartz sand, zeolite, and anthracite) commonly found in water plants were used. The retention patterns of PS-MPs by various filter media under various background water quality conditions were methodically investigated with the aid of DLVO theory and colloidal filtration theory. The results show that the different structures and elemental compositions of the three filter media cause them to exhibit different surface roughnesses and surface potentials. A greater surface roughness of the filter media can provide more deposition sites for PS-MPs, and the greater surface roughness of zeolite and anthracite significantly enhances their ability to inhibit the migration of PS-MPs compared with that of quartz sand. However, surface roughness is not the only factor affecting the migration of MPs. The lower absolute value of the surface potential of anthracite causes the DLVO energy between it and PS-MPs to be significantly lower than that between zeolite and PS-MPs, which results in stronger retention of PS-MPs by anthracite, which has a lower surface roughness, than zeolite, which has a higher surface roughness. The transport of PS-MPs in the medium is affected by the combination of the surface roughness of the filter media and the DLVO energy. Under the same operating conditions, the retention efficiencies of the three filter materials for PS-MPs followed the order of quartz sand < zeolite < anthracite. Additionally, the conditions of the solution markedly influenced the transport ability of PS-MPs within the simulated filter column. The transport PS-MPs in the simulated filter column decreased with increasing solution ionic strength and cation valence. Naturally, dissolved organic matter promoted the transfer of PS-MPs in the filter layer, and humic acid had a much stronger facilitating impact than fulvic acid. The study findings might offer helpful insight for improving the ability of filter units ability to retain MPs.

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