In this study the BEST7 software was employed to quantify different classes of functional groups and to model the proton titration behavior of humic substances. To illustrate the process, the Suwannee River fulvic acid of the IHSS (International Humic Substances Society) was used. Five categories-two classes of phenolic groups (phenol and cathecol), two classes of carboxylic groups (benzoic and phtalic) and the combination between them (salicylic)-of oxygenated groups were considered as being responsible for the potentiometric behavior of the sample and were quantitatively determined. The most and the least abundant-1-1 groups were cathecol (3.300 0.010 mmol g) and phenol (1.225 0.070 mmol g), respectively. The estimated equilibrium constants were also determined and were in good agreement with the literature values for phenol and cathecol groups and for benzoic, phtalic and salicylic acids. Distribution diagrams of the species were generated with the software SPE and SPEPLOT.
In this work, the interactions of the functional groups of fulvic acids with copper, cadmium and zinc bivalent ions was investigated by potentiometry. The BEST7 software was employed to investigate the interactions of the functional groups. The software SPE and SPEPLOT were used to generate and to plot the species diagrams. It was used the Suwannee River fulvic acid (SRFA) of the IHSS (International Humic Substances Society) to illustrate the process. The values of the proton dissociation and complexation constants with the divalent ions for each functional group were calculated and their values were very close tothose previously published. The functional group present in the highest quantity in the complexes was cathecol, and it complexed with all the divalent ions, although to a greater extent with Cu(II). According to the results obtained by potentiometry, the reactivity series for the divalent ions and the SRFA is: Cu(II) >> Cd(II) > Zn(II). Thus, the method employed could be useful to estimate the role of fulvic acids in the transport of metals in the aquatic environments.
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