Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
608355 | Journal of Colloid and Interface Science | 2012 | 7 Pages |
Enrofloxacin (ENR) occurs widely in natural waters because of its extensive use as a veterinary chemotherapeutic agent. To improve our understanding of the interaction of this emerging contaminant with soils and sediments, sorption of ENR on homoionic smectites and kaolinite was studied as a function of pH, ionic strength, exchangeable cations, and humic acid concentration. Batch experiments and in situ ATR–FTIR analysis suggested multiple sorption mechanisms. Cation exchange was a major contributor to the sorption of cationic ENR species on smectite. The decreased ENR sorption with increasing ionic strength indicated the formation of outer-sphere complexes. Exchangeable cations significantly influenced the sorption capacity, and the observed order was Cs < Ca < K. The peak shifts of the COO− stretch, coupled CO stretch and OH deformation, and the result of irreversible desorption FTIR spectra indicated that OH of the carboxyl group was involved in the formation of inner-sphere surface complexes. The XRD analysis confirmed that interlayer intercalation is an important contributor to ENR sorption, while humic acid had a negligible contribution to the interlayer intercalation. The results of this study provide new insight into the molecular mechanisms of ENR sorption on clay minerals.
Graphical abstractFigure optionsDownload full-size imageDownload high-quality image (90 K)Download as PowerPoint slideHighlights► Multiple sorption mechanisms are responsible for the high ENR sorption capacity. ► pH, ionic strength, and clay conformation affect surface and interlayer sorption. ► Cation selectivity and hydrophobic sites on clay surface control ENR sorption.