Fluoride removal from aqueous solution by Zirconium-Chitosan/Graphene Oxide Membrane

A Zirconium-Chitosan/Graphene Oxide (Zr-CTS/GO) Membrane adsorbent was applied for fluoride removal from aqueous solution. The effects of different compositions, dose, pH, and initial fluoride concentration were investigated. Results showed that the membrane could effectively remove fluoride within...

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Veröffentlicht in:Reactive & functional polymers 2017-05, Vol.114, p.127-135
Hauptverfasser: Zhang, Jing, Chen, Nan, Su, Panyun, Li, Miao, Feng, Chuanping
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Sprache:eng
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Zusammenfassung:A Zirconium-Chitosan/Graphene Oxide (Zr-CTS/GO) Membrane adsorbent was applied for fluoride removal from aqueous solution. The effects of different compositions, dose, pH, and initial fluoride concentration were investigated. Results showed that the membrane could effectively remove fluoride within a wide pH range of 3–11. The data fitted the Freundlich isotherm model well, indicating that fluoride adsorption occurred on heterogeneous Zr-CTS/GO membrane surfaces probably in a multilayer form. The kinetic studies showed that the adsorption reached equilibrium within 45min, and the maximum adsorption capacity was calculated to be 29.0588mg/g by Two-site Langmuir isotherm model. X-ray photoelectron spectroscopy (XPS), and extended X-ray absorption fine structure spectroscopy (EXAFS) were used to elucidate the adsorption mechanism. The results revealed that Zr(IV) species reacted with oxygen functional groups from the CTS/GO complex, and ZrF species formed partly through fluoride ions exchanged with chloride ions and OH and partly through chemical rearrangement. The findings indicate that Zr-CTS/GO is a promising adsorbent for fluoride removal with a quite short contact time and a wide optimum pH range. •Zr-CTS/GO was synthesized and showed high performance for fluoride removal.•ATR-FTIR, XPS, and EXAFS analyses were used to elucidate the adsorption mechanism.•Amino groups in CTS reacted with carboxyl and epoxy groups in GO.•Fluoride removal via ion exchange and chemical rearrangement to form ZrF species [Display omitted]
ISSN:1381-5148
1873-166X
DOI:10.1016/j.reactfunctpolym.2017.03.008