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

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• 作者：Weiping Xiong^a ; ^b ; Jing Tong^a ; ^b ; Zhaohui Yang^a ; ^b ; ^{yzh@hnu.edu.cn} ; Guangming Zeng^a ; ^b ; ^{zgming@hnu.edu.cn} ; Yaoyu Zhou^c ; Dongbo Wang^a ; ^b ; Peipei Song^a ; ^b ; Rui Xu^a ; ^b ; Chen Zhang^a ; ^b ; Min Cheng^a ; ^b
• 关键词：Phosphate ; Adsorption ; Iron ; Zirconium ; Activated carbon nanofiber
• 刊名：Journal of Colloid and Interface Science
• 出版年：2017
• 出版时间：1 May 2017
• 年：2017
• 卷：493
• 期：Complete
• 页码：17-23
• 全文大小：1238 K
• 卷排序：493

文摘

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 °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.