4.7 Article

Adsorption of phosphate from aqueous solution using iron-zirconium modified activated carbon nanofiber: Performance and mechanism

Journal

JOURNAL OF COLLOID AND INTERFACE SCIENCE
Volume 493, Issue -, Pages 17-23

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2017.01.024

Keywords

Phosphate; Adsorption; Iron; Zirconium; Activated carbon nanofiber

Funding

  1. National Natural Science Foundation of China [51521006, 51378190]
  2. Program for Changjiang Scholars and Innovative Research Team in University [IRT-13R17]
  3. Fundamental Research Funds for the Central Universities

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Phosphate (P) removal is significant for the prevention of eutrophication in natural waters. In this paper, a novel adsorbent for the removal of P from aqueous solution was synthesized by loading zirconium oxide and iron oxide onto activated carbon nanofiber (ACF-ZrFe) simultaneously. The adsorbent was characterized by scanning electron microscopy (SEM), Fourier transform infrared (FT-IR) spectroscopy and X-ray photoelectron spectroscopy (XPS). The results showed that P adsorption was highly pH dependent and the optimum pH was found to be 4.0. The isotherm of adsorption could be well described by the Langmuir model and the maximum P adsorption capacity was estimated to be 26.3 mg P/g at 25 degrees C. The kinetic data were well fitted to the pseudo-second-order equation, indicating that chemical sorption was the rate-limiting step. Moreover, co-existing ions including sulfate (SO42-), chloride (cl(-)), nitrate (NO3-) and fluoride (F-) exhibited a distinct effect on P adsorption with the order of F- > NO3- > Cl- > SO42-. Further investigations by FT-IR spectroscopy and pH variations associated with the adsorption process revealed that ligands exchange and electrostatic interactions were the dominant mechanisms for P adsorption. The findings reported in this work highlight the potential of using ACF-ZrFe as an effective adsorbent for the removal of P in natural waters. (C) 2017 Elsevier Inc. All rights reserved.

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