Adsorption characteristics and mechanisms of water-soluble polymers (PVP and PEG) on kaolin and montmorillonite minerals

Journal Article (2024)
Author(s)

Xintu Wang (Chinese Academy of Sciences, Guilin University of Technology)

Yanghui Xu (TU Delft - Sanitary Engineering, Chinese Academy of Sciences)

Qin Ou (Chinese Academy of Sciences, TU Delft - Sanitary Engineering)

Wenwen Chen (Guilin University of Technology)

Walter van der Meer (University of Twente, Oasen)

Gang Liu (TU Delft - Sanitary Engineering, Chinese Academy of Sciences)

DOI related publication
https://doi.org/10.1016/j.jhazmat.2024.133592 Final published version
More Info
expand_more
Publication Year
2024
Language
English
Volume number
466
Article number
133592
Downloads counter
423
Collections
Institutional Repository
Reuse Rights

Other than for strictly personal use, it is not permitted to download, forward or distribute the text or part of it, without the consent of the author(s) and/or copyright holder(s), unless the work is under an open content license such as Creative Commons.

Abstract

The excessive use and accumulation of water-soluble polymers (WSPs, known as “liquid plastics”) in the environment can pose potential risks to both ecosystems and human health, but the environmental fate of WSPs remains unclear. Here, the adsorption behavior of WSPs with different molecular weight on kaolinite (Kaol) and montmorillonite (Mt) were examined. The results showed that the adsorption of PEG and PVP on minerals were controlled by hydrogen bond and van der Waals force. The Fourier transform infrared (FTIR) spectra and two-dimensional correlation spectroscopy (2D-COS) analysis revealed that there were interactions between the Al-O and Si-O groups of the minerals and the polar O- or N-containing functional groups as well as the alkyl groups of PEG and PVP. The adsorption characteristics of WSPs were closely related to their molecular weight and the pore size of minerals. Due to the relatively large mesopore size of Kaol, both PEG and PVP were absorbed into inner spaces, for which the adsorption capacity increased with molecular weight of the polymers. For Mt, all types of PEG could enter its micropores, while PVP with larger molecular weights appeared to be confined externally, leading to a decrease in the adsorption capacity of PVP with increasing molecular weight. The findings of this study provide a theoretical basis for scientific evaluation of environmental processes of WSPs.