Published November 15, 2009 | Version v1
Journal article

Fluoride adsorption onto granular ferric hydroxide: Effects of ionic strength, pH, surface loading, and major co-existing anions

  • 1. Department of Civil, Architectural and Environmental Engineering, Missouri University of Science and Technology, Rolla, MO 65409 (United States)
  • 2. College of Environmental Science and Engineering, Tongji University, 1239 Siping Road, Shanghai 200092 (China)
  • 3. State Key Lab of Urban Water Resource and Environment (HIT), Harbin Institute of Technology, Harbin 150090 (China)
  • 4. Department of Chemistry, Missouri University of Science and Technology, Rolla, MO 65409 (United States)

Description

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-.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jhazmat.2009.06.079

Additional details

Identifiers

DOI
10.1016/j.jhazmat.2009.06.079;
PII
S0304-3894(09)00991-1;

Publishing Information

Journal Title
Journal of Hazardous Materials
Journal Volume
171
Journal Issue
1-3
Journal Page Range
p. 774-779
ISSN
0304-3894
CODEN
JHMAD9

Optional Information

Copyright
Copyright (c) 2009 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.