Competitive adsorption involving phosphate and benzenecarboxylic acids on goethite-Effects of molecular structures

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T1 - Competitive adsorption involving phosphate and benzenecarboxylic acids on goethite-Effects of molecular structures

AU - Lindegren, Malin

AU - Persson, Per

N1 - 1

PY - 2010

Y1 - 2010

N2 - The competitive adsorption between phosphate and either one of seven benzenecarboxylates (benzoate, phthalate, trimellitate, trimesoate, hemimellitate, pyromellitate, and mellitate) on the surfaces of fine-particulate goethite (alpha-FeOOH) was investigated as a function of pH. The series of ligands contained Molecules with an increasing number of functional groups as well as three structural isomers of the tricarboxylates. Thus, the effects of both the number of carboxylate groups and the relative positions of these groups on the competitive efficiency toward phosphate were probed ill this Study. Quantitative adsorption experiments in batch mode and infrared spectroscopy were collectively Used to evaluate the competitive adsorption reactions. Under the conditions probed, mono- and dicarboxylates had no detectable effect on phosphate adsorption whereas the ligands containing three or more carboxylate groups were able to partially outcompete phosphate. However, the pH dependency and the extent of these competitive effects were strongly dependent on (lie structure and composition of the benzenecarboxylate. The collective results showed that it was the competition for hydrogen-bonding surface sites rather than inner sphere Surface sites that primarily determined the outcome of the competitive adsorption experiments,and it was the ability of the organic ligand to act as hydrogen-bonding acceptor and/or donor in various parts of the pH range that also determined the competitive pH dependency. The importance of H-bonding for the competitive adsorption between phosphate and benzenecarboxylic acids suggested that H-bonding interactions contributed substantially to the stabilities of both the adsorbed benzenecarboxylates and the phosphate ions and that these interactions were structurally specific: i.e., they were sensitive to the locations and the directional properties of the H-acceptor and H-donor surface sites. (c) 2009 Elsevier Inc. All rights reserved.

AB - The competitive adsorption between phosphate and either one of seven benzenecarboxylates (benzoate, phthalate, trimellitate, trimesoate, hemimellitate, pyromellitate, and mellitate) on the surfaces of fine-particulate goethite (alpha-FeOOH) was investigated as a function of pH. The series of ligands contained Molecules with an increasing number of functional groups as well as three structural isomers of the tricarboxylates. Thus, the effects of both the number of carboxylate groups and the relative positions of these groups on the competitive efficiency toward phosphate were probed ill this Study. Quantitative adsorption experiments in batch mode and infrared spectroscopy were collectively Used to evaluate the competitive adsorption reactions. Under the conditions probed, mono- and dicarboxylates had no detectable effect on phosphate adsorption whereas the ligands containing three or more carboxylate groups were able to partially outcompete phosphate. However, the pH dependency and the extent of these competitive effects were strongly dependent on (lie structure and composition of the benzenecarboxylate. The collective results showed that it was the competition for hydrogen-bonding surface sites rather than inner sphere Surface sites that primarily determined the outcome of the competitive adsorption experiments,and it was the ability of the organic ligand to act as hydrogen-bonding acceptor and/or donor in various parts of the pH range that also determined the competitive pH dependency. The importance of H-bonding for the competitive adsorption between phosphate and benzenecarboxylic acids suggested that H-bonding interactions contributed substantially to the stabilities of both the adsorbed benzenecarboxylates and the phosphate ions and that these interactions were structurally specific: i.e., they were sensitive to the locations and the directional properties of the H-acceptor and H-donor surface sites. (c) 2009 Elsevier Inc. All rights reserved.

U2 - 10.1016/j.jcis.2009.11.040

DO - 10.1016/j.jcis.2009.11.040

M3 - Article

VL - 343

SP - 263

EP - 270

JO - Journal of Colloid and Interface Science

T2 - Journal of Colloid and Interface Science

JF - Journal of Colloid and Interface Science

SN - 0021-9797

ER -