4.2 Article

A mechanistic study of ciprofloxacin adsorption by goethite in the presence of silver and titanium dioxide nanoparticles

Journal

JOURNAL OF ENVIRONMENTAL SCIENCES
Volume 118, Issue -, Pages 46-56

Publisher

SCIENCE PRESS
DOI: 10.1016/j.jes.2021.08.052

Keywords

Ciprofloxacin; Goethite; Silver nanoparticles; Titanium dioxide nanoparticles; Adsorption

Funding

  1. National Key Research and Development Program of China [2020YFC1808300]
  2. Fundamental Research Fund for the Central Uni-versities [2652019115]
  3. Guangxi Key Research Project [GuikeAB18050026]
  4. Natural Science Foundation of China [41731282]

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This study investigated the adsorption behaviors of ciprofloxacin onto goethite in the presence of silver and titanium dioxide nanoparticles. The results showed that the presence of nanoparticles inhibited the adsorption of ciprofloxacin by goethite, and the mechanisms of inhibition were different for silver and titanium dioxide nanoparticles.
The adsorption behaviors of ciprofloxacin (CIP), a fluoroquinolone antibiotic, onto goethite (Gt) in the presence of silver and titanium dioxide nanoparticles (AgNPs and TiO(2)NPs) were investigated. Results showed that CIP adsorption kinetics in Gt with or without NPs both followed the pseudo-second-order kinetic model. The presence of AgNPs or TiO(2)NPs inhibited the adsorption of CIP by Gt. The amount of inhibition of CIP sorption due to AgNPs was decreased with an increase of solution pH from 5.0 to 9.0. In contrast, in the presence of TiO(2)NPs, CIP adsorption by Gt was almost unchanged at pHs of 5.0 similar to 6.5 but was decreased with an increase of pH from 6.5 to 9.0. The mechanisms of AgNPs and TiO(2)NPs in inhibiting CIP adsorption by Gt were different, which was attributed to citrate coating of AgNPs resulting in competition with CIP for adsorption sites on Gt, while TiO(2)NPs could compete with Gt for CIP adsorption. Additionally, CIP was adsorbed by Gt or TiO(2)NPs through a tridentate complex involving the bidentate inner-sphere coordination of the deprotonated carboxylic group and hydrogen bonding through the adjacent carbonyl group on the quinoline ring. These findings advance our understanding of the environmental behavior and fate of fluoroquinolone antibiotics in the presence of NPs. (C) 2022 The Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences. Published by Elsevier B.V.

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