Cheng, Jun

Liu, Xiandong

Lu, Xiancai

Meijer, Evert Jan

Sprik, Michiel

Wang, Rucheng

Geochimica et Cosmochimica Acta

English

Liu, X.

Lu, X.

Sprik, M.

Cheng, J.

Meijer, E.J.

Wang, R.

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Acidity of edge surface sites of montmorillonite and kaolinite

Acid-base chemistry of clay minerals is central to their interfacial properties, but up to now a quantitative understanding on the surface acidity is still lacking. In this study, with first principles molecular dynamics (FPMD) based vertical energy gap technique, we calculate the acidity constants of surface groups on (010)-type edges of montmorillonite and kaolinite, which are representatives of 2:1 and 1:1-type clay minerals, respectively. It shows that Si-OH and Al-OH2OH groups of kaolinite have pKas of 6.9 and 5.7 and those of montmorillonite have pKas of 7.0 and 8.3, respectively. For each mineral, the calculated pKas are consistent with the experimental ranges derived from fittings of titration curves, indicating that Si-OH and Al-OH2OH groups are the major acidic sites responsible to pH-dependent experimental observations. The effect of Mg substitution in montmorillonite is investigated and it is found that Mg substitution increases the pKas of the neighboring =Si-OH and =Si-OH2 groups by 2-3 pKa units. Furthermore, our calculation shows that the pKa of edge, =Mg-(OH2)(2) is as high as 13.2, indicating the protonated state dominates under common pH. Together with previous adsorption experiments, our derived acidity constants suggest that Si-O-and Al (OH)(2) groups are the most probable edge sites for complexing heavy metal cations

Acidity of edge surface sites of montmorillonite and kaolinite

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