4.7 Article

Co-adsorption of ciprofloxacin and Cu(II) onto titanate nanotubes: Speciation variation and metal-organic complexation

Journal

JOURNAL OF MOLECULAR LIQUIDS
Volume 292, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.molliq.2019.111375

Keywords

Titanate nanotubes; Heavy metal; Emerging organic contaminant; Adsorption; Complexation; Interaction mechanism

Funding

  1. National Natural Science Foundation of China [51508006, 91647211, 51721006]

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Titanate nanotubes (TNTs) have been reported to show good adsorption performance for heavy metals, but researches on organic contaminants adsorption by TNTs are limited. In this study, co-adsorption of a heavy metal (Cu) and an emerging organic contaminant (ciprofloxacin, CIP) by TNTs was investigated in binary systems. TNTs could simultaneously remove the two contaminants, with a high adsorption capacity of 234.5 mu mol/g for Cu(II) and 237.0 mu mol/g for CIP at pH 4 in the binary system. pH greatly affected adsorption due to speciation variation of the contaminants and surface charge change of TNTs. Cu(II)-CIP complexes dominated adsorption capacity and mechanism. Adsorption of CIP was promoted by high concentration of Cu(II) at pH 3-8 due to formation of abundant Cu(CIP +/-)(2+), while inhibited by low concentration of Cu(II) because of competitive adsorption. The adsorption affinity of CIP species to TNTs was ranked as: Cu(CIP +/-)(2+) > CIP+ > CIP +/- > Cu(CIP +/-)(2)(+) > Cu(CIP- center dot( ) CIP +/-)(+) > CIP-. In comparison, the co-existence of CIP slightly affected Cu(II) adsorption considering the strong affinity of Cu2+ to TNTs. X-ray photoelectron spectrometer (XPS) and Fourier transform infrared spectroscopy (FIR) results further confirmed the formation of Cu(II)-CIP complexes through -NH2 Cu/-COOCu linkages. This work not only proposed a feasible technology for co-removal of heavy metals and organics from water, but also presented insight into interaction mechanisms of different contaminants with nanomaterials during adsorption. (C) 2019 Elsevier B.V. All rights reserved.

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