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Adsorption mechanism and influencing factors of selenium under the coexistence of nanoparticles and microplastics.

Authors :
Jian-jun Lian
Shun Jiang
Hua-fei Si
Qiong-jie Wang
Hong-yan Wu
Xin-zhu Hong
Qiao-ping Kong
Bo Chen
Source :
Desalination & Water Treatment; Apr2024, Vol. 318, p1-9, 9p
Publication Year :
2024

Abstract

Microplastics (MPs), as a common "vector" of pollutants in the aquatic environment, have a significant impact on the migration and transformation of heavy metals. In order to explore the mechanism and the influencing factors of the adsorption behavior of microplastics (MPs) on selenium (Se) in aqueous solution under the coexistence of nanoparticles, polystyrene microplastics (PS), nano-titanium dioxide particles (TiO<subscript>2</subscript>) and their coexisting compounds (PS + TiO<subscript>2</subscript>) were used as adsorbents to investigate the adsorption kinetics, isotherms and thermodynamic processes of Se. The effects of pH, humic acid concentration and coexisting ions on the ad-sorption behavior of Se(VI) were also analyzed. The results showed that the adsorption process of Se(VI) by PS and PS + TiO<subscript>2</subscript> could be well fitted by pseudo-second-order kinetic model and Freundlich isotherm model, and it was an endothermic reaction with increased entropy. The adsorption capacity of Se(VI) by PS, TiO<subscript>2</subscript>, and PS + TiO<subscript>2</subscript> were decreased with the increase of solution pH. Humic acid and Ca<superscript>2+</superscript> promoted the adsorption of Se (VI), while PO<subscript>4</subscript><superscript>3-</superscript> significantly inhibited the adsorption of Se(VI) in the above three systems. The main adsorption mechanism of PS on Se(VI) was electrostatic adsorption and hydrogen bonding. The TiO<subscript>2</subscript> adsorbed on the surface of PS mainly affected the adsorption behavior of PS on Se(VI) through hydrogen bonding. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
19443994
Volume :
318
Database :
Complementary Index
Journal :
Desalination & Water Treatment
Publication Type :
Academic Journal
Accession number :
177831552
Full Text :
https://doi.org/10.1016/j.dwt.2024.100338