Cr. Evanko et Da. Dzombak, INFLUENCE OF STRUCTURAL FEATURES ON SORPTION OF NOM-ANALOG ORGANIC-ACIDS TO GOETHITE, Environmental science & technology, 32(19), 1998, pp. 2846-2855
A systematic study of the role of structural features of NOM-analogue
organic acids in influencing mineral-organic acid interactions was per
formed. Goethite, a crystalline form of iron oxide important in geoche
mical systems, was employed as a model mineral. Sorption experiments w
ith a series of small molecular weight, aromatic organic acids were pe
rformed to assess the effects of particular features of compound struc
ture on sorption to goethite and to obtain insight into the kinds of s
urface reactions responsible for organic acid sorption, important func
tional groups of the humic acid component of NOM were examined. Experi
ments were also performed with Aldrich humic acid to allow comparison
between sorption behavior of simple organic acids and NOM and to deter
mine suitable analogues for modeling NOM sorption. Sorption characteri
stics far most organic acids were typical for anionic sorbates, with h
igh sorption at low pH and decreasing sorption as pH increased. Sorpti
on of simple organic acids exhibited strong dependence on the number,
type, and position of reactive functional groups, and compounds having
particular structural features in common exhibited similar sorption b
ehavior. The important structural characteristics governing sorption o
f simple aromatic organic acids appeared to be adjacent carboxylic gro
ups, adjacent phenolic groups, phenolic groups in the ortho position r
elative to a carboxylic group, and overall acidity of the compound. Or
ganic acid sorption also appeared to be influenced by hydrophobic inte
ractions for some of the compounds. NOM sorption was best mimicked by
1,2,4,5-benzenetetracarboxylic acid (pyromellitic acid) and 2,3-dihydr
oxybenzoic acid. Compounds having a combination of the structural feat
ures present on these organic acids might better represent NOM sorptio
n.