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Environmental Science and Pollution Research

, Volume 26, Issue 11, pp 11170–11178 | Cite as

Effect of cation type in mixed Ca-Na systems on transport of sulfonamide antibiotics in saturated limestone porous media

  • Kaixuan Sun
  • Yuanyuan SunEmail author
  • Bin Gao
  • Hongxia Xu
  • Jichun WuEmail author
Research Article
  • 146 Downloads

Abstract

Retention and transport of sulfonamides (SAs) in subsurface can strongly affect groundwater quality. In this work, a range of laboratory batch sorption and column transport experiments were conducted to determine the effect of cation type in mixed Ca-Na systems on the retention and transport of two typical SAs, sulfadimethoxine (SDM) and sulfacetamide (SCA), in saturated limestone porous media. Column experimental data showed divalent cation Ca2+ played a more important role than monovalent cation Na+ in decreasing the transport of only SDM in co-cation systems in the saturated limestone media. Further, in the single-cation (i.e., including either Ca2+ or Na+) system, increasing ionic strength (IS) of either NaCl or CaCl2 had little effect on SCA transport; however, increasing of IS of CaCl2 promoted the retention of SDM in the saturated limestone porous media. This is mainly due to the cation bridging effect of Ca2+ on SDM and limestone. Overall, SDM showed much higher retention in the limestone columns than SCA, which can be attributed to the two SAs’ different physicochemical properties. Moreover, limestone showed stronger ability to retain the two SAs than quartz sand. Findings in this study suggest that cation type and the concentration of certain electrolyte (e.g., CaCl2) as well as medium type play an important role in controlling the environmental fate and transport of antibiotics.

Keywords

Sorption Ionic strength Leaching Breakthrough curves Column experiments Medium type 

Notes

Funding information

This study was supported by the National Key Research and Development Program of China (2018YFC0406401-2); the National Nature Science Foundation of China (41730856); the National Nature Science Foundation of China-Xinjiang Project (U1503282); and the Program B for Outstanding Ph. D candidate of Nanjing University (201802B084).

Supplementary material

11356_2019_4561_MOESM1_ESM.docx (212 kb)
ESM 1 (DOCX 211 kb)

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Copyright information

© Springer-Verlag GmbH Germany, part of Springer Nature 2019

Authors and Affiliations

  1. 1.Key Laboratory of Surficial Geochemisty, Ministry of Education, School of Earth Sciences and EngineeringNanjing UniversityNanjingChina
  2. 2.Department of Agricultural and Biological EngineeringUniversity of FloridaGainesvilleUSA

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