Sorption behavior of oxytetracycline on microplastics and the influence of environmental factors in groundwater: Experimental investigation and molecular dynamics simulation.

J Contam Hydrol

School of Water and Environment, Chang'an University, Xi'an 710054, China; Key Laboratory of Subsurface Hydrology and Ecology in Arid Areas, Ministry of Education, Chang'an University, Xi'an 710054, China; Key Laboratory of Eco-hydrology and Water Security in Arid and Semi-arid Regions of Ministry of Water Resources, Chang'an University, Xi'an 710054, China. Electronic address:

Published: December 2024

Microplastics (MPs) and antibiotics can enter groundwater through the interaction of soil and surface water, and MPs as carriers of antibiotics can promote the migration of antibiotics and thus generate more serious ecological risks. Therefore, this paper used experimental and molecular dynamics (MD) simulation methods to investigate the sorption between four common types of MPs in groundwater, namely polyamide (PA), polystyrene (PS), polyvinyl chloride (PVC), and polyethylene (PE), and oxytetracycline (OTC) with high detection rate in groundwater. Additionally, the impact of environmental factors on sorption was examined. The sorption kinetics of the four types of MPs followed the pseudo-second-order kinetics model, and the sorption isotherms of OTC on PA, PE, and PVC were highly linear, suggesting that the electrostatic interaction was the main sorption mechanism. Both experimental and simulation results indicated that PA had the highest affinity for OTC, due to the effect of the formation of hydrogen bonding between the amide groups of PA and OTC. The primary way pH affected sorption was by altering the form in which OTC exists. The effects of the representative substances of protein-like component (bovine serum albumin) and humus-like component (humic acid) in dissolved organic matter varied but were generally inhibitory. Ions could influence the sorption process by competitive sorption or forming complexes with the OTC.

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Source
http://dx.doi.org/10.1016/j.jconhyd.2024.104489DOI Listing

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