Literature DB >> 28088117

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

Weiping Xiong1, Jing Tong1, Zhaohui Yang2, Guangming Zeng3, Yaoyu Zhou4, Dongbo Wang1, Peipei Song1, Rui Xu1, Chen Zhang1, Min Cheng1.   

Abstract

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 26.3mgP/g at 25°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.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Activated carbon nanofiber; Adsorption; Iron; Phosphate; Zirconium

Mesh:

Substances:

Year:  2017        PMID: 28088117     DOI: 10.1016/j.jcis.2017.01.024

Source DB:  PubMed          Journal:  J Colloid Interface Sci        ISSN: 0021-9797            Impact factor:   8.128


  10 in total

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