Understanding arsenate reaction kinetics with ferric hydroxides

James Farrell, Binod K. Chaudhary

Research output: Contribution to journalArticle

43 Citations (Scopus)

Abstract

Understanding arsenic reactions with ferric hydroxides is important in understanding arsenic transport in the environment and in designing systems for removing arsenic from potable water. Many experimental studies have shown that the kinetics of arsenic adsorption on ferric hydroxides is biphasic, where a fraction of the arsenic adsorption occurs on a time scale of seconds while full equilibrium may require weeks to attain. This research employed density functional theory modeling in order to understand the mechanisms contributing to biphasic arsenic adsorption kinetics. The reaction energies and activation barriers for three modes of arsenate adsorption to ferric hydroxides were calculated. Gibbs free energies of reaction depended on the net charge of the complexes, which is a function of the system pH value. Physical adsorption of arsenate to ferric hydroxide proceeded with no activation barrier, with Gibbs free energies of reaction ranging from -21 to -58 kJ/mol. The highest Gibbs free energies of reaction for physical adsorption resulted from negative charge assisted hydrogen bonding between H atoms on the ferric hydroxide and O atoms in arsenate. The conversion of physically adsorbed arsenate into monodentate surface complexes had Gibbs free energies of activation ranging from 62 to 73 kJ/mol, and Gibbs free energies of reaction ranging from -23 to -38 kJ/mol. The conversion of monodentate surface complexes to bidentate, binuclear complexes had Gibbs free energies of activation ranging from 79 to 112 kJ/mol and Gibbs free energies of reaction ranging from -11 to -55 kJ/mol. For release of arsenate from uncharged bidentate complexes, energies of activation as high as 167 kJ/mol were encountered. Increasingly negative charges on the complexes lowered the activation barriers for desorption of arsenate, and in complexes with -2 charges, the highest activation barrier was 65 kJ/mol. This study shows that the slow kinetics associated with arsenic adsorption and desorption can be attributed to the high Gibbs free energies of activation for forming and breaking bonds with the ferric hydroxide.

Original languageEnglish (US)
Pages (from-to)8342-8347
Number of pages6
JournalEnvironmental Science and Technology
Volume47
Issue number15
DOIs
StatePublished - Aug 6 2013

Fingerprint

Gibbs free energy
reaction kinetics
arsenate
Reaction kinetics
Arsenic
hydroxide
Chemical activation
arsenic
adsorption
Adsorption
kinetics
Kinetics
Desorption
desorption
Atoms
arsenic acid
ferric hydroxide
Drinking Water
Density functional theory
energy

ASJC Scopus subject areas

  • Chemistry(all)
  • Environmental Chemistry

Cite this

Understanding arsenate reaction kinetics with ferric hydroxides. / Farrell, James; Chaudhary, Binod K.

In: Environmental Science and Technology, Vol. 47, No. 15, 06.08.2013, p. 8342-8347.

Research output: Contribution to journalArticle

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