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

J Hazard Mater. 2009 Nov 15;171(1-3):774-9. doi: 10.1016/j.jhazmat.2009.06.079. Epub 2009 Jun 21.

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: H(2)PO(4)(-)>HCO(3)(-)>SO(4)(2-)>Cl(-).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adsorption
  • Anions
  • Ferric Compounds / chemistry*
  • Fluorides / chemistry*
  • Hydrogen-Ion Concentration
  • Ions
  • Spectrophotometry, Infrared / methods
  • Surface Properties
  • Time Factors
  • Water Pollutants, Chemical / analysis
  • Water Pollutants, Chemical / isolation & purification*
  • Water Purification / methods*
  • Water Supply

Substances

  • Anions
  • Ferric Compounds
  • Ions
  • Water Pollutants, Chemical
  • ferric hydroxide
  • Fluorides