Adsorption of Humic Substances on Goethite:  Comparison between Humic Acids and Fulvic Acids

The adsorption of humic acids (HA) to goethite (at pH 3−11) and the proton co-adsorption (at pH 4.0, 5.5, and 7.0) were measured, and the results were compared to those of fulvic acids (FA). Compared to FA, the adsorption of HA is stronger and more ionic strength dependent. The adsorption of both HA...

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Published inEnvironmental science & technology Vol. 40; no. 24; pp. 7494 - 7500
Main Authors Weng, Van Riemsdijk, Willem H, Koopal, Luuk K, Hiemstra, Tjisse
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 15.12.2006
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Summary:The adsorption of humic acids (HA) to goethite (at pH 3−11) and the proton co-adsorption (at pH 4.0, 5.5, and 7.0) were measured, and the results were compared to those of fulvic acids (FA). Compared to FA, the adsorption of HA is stronger and more ionic strength dependent. The adsorption of both HA and FA decreases with increasing pH. The relative change of the adsorption with pH is bigger for HA than for FA at relatively low pH. At relatively high pH, it is the opposite. Protons are released at pH 4.0 and co-adsorbed at pH 5.5 and 7.0 upon the adsorption of both HA and FA. The observed pH dependency of HA and FA adsorption is in agreement with the proton co-adsorption data. Model calculations show that the adsorbed FA particles are on average located in the Stern layer, whereas the adsorbed HA particles protrude beyond the Stern layer. The closer location to the surface of the adsorbed FA leads to stronger electrostatic interactions between the FA particles and the surface, which explains the larger amount of protons released at low pH and co-adsorbed at high pH with each mass unit of FA adsorbed than that with HA adsorbed. The model also reveals that for FA a mean-field (smeared-out) approximation is reasonable, but for HA a patchwise approach is more appropriate at relatively low loading.
Bibliography:This article is part of the Modeling Natural Organic Matter Focus Group.
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ISSN:0013-936X
1520-5851
DOI:10.1021/es060777d