Fluoride Adsorption Onto Granular Ferric Hydroxide: Effects of Ionic Strength, PH, Surface Loading, and Major Co-Existing Anions
Abstract
Fluoride adsorption onto granular ferric hydroxide (GFH) was investigated using batch methods, under various ionic strength, pH, surface loading, and major co-existing anion conditions. Adsorption of fluoride on GFH included an initial fast adsorption phase followed by a slow adsorption phase. within the pH range of 2-11, fluoride adsorption equilibrium was not affected by ionic strength, but was significantly affected by pH. Maximum adsorption was achieved in the pH range of 3-6.5. under the same pH condition, fluoride adsorption followed the Freundlich isotherm, indicating that the GFH surface was heterogeneous. X-ray photoelectron spectroscopy (XPS) and attenuated total reflection-infrared (ATR-IR) spectroscopy data showed evidence for fluoride sorption on the GFH surface via inner-sphere complexation accompanying increased hydrogen bonding and surface hydroxylation. Major anions, including phosphate, bicarbonate, sulfate, and chloride, reduced fluoride adsorption in the following order: H2PO4- > HCO3- > SO42- > Cl-.
Recommended Citation
Y. Tang et al., "Fluoride Adsorption Onto Granular Ferric Hydroxide: Effects of Ionic Strength, PH, Surface Loading, and Major Co-Existing Anions," Journal of Hazardous Materials, Elsevier, Nov 2009.
The definitive version is available at https://doi.org/10.1016/j.jhazmat.2009.06.079
Department(s)
Civil, Architectural and Environmental Engineering
Second Department
Chemistry
Sponsor(s)
China Scholarship Council
Missouri University of Science and Technology. Environmental Research Center
University of Missouri Research Board
Keywords and Phrases
XPS; Granular Ferric Hydroxide; Ionic Strength; pH; Adsorption; Fluorides; X-ray photoelectron spectroscopy
International Standard Serial Number (ISSN)
0304-3894
Document Type
Article - Journal
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 2009 Elsevier, All rights reserved.
Publication Date
01 Nov 2009