Reaction sequence of Nickel(II) with kaolinite: Mineral dissolution and surface complexation and precipitation

The dissolution kinetics of NI(II) sorbed to kaolinite at pH 7 were examined as a function of initial aqueous NI(II) concentrations; the local molecular structure of the Ni surface complexes were determined using extended x-ray absorption fine structure (EXAFS) spectroscopy. The dissolution of kaolinite was nonstoichiometric with a preferential release of Si over Al. The dissolution rate, R-sl, increased with an increase in the aqueous concentration of Ni. A rate law was developed representing a fractional-order dissolution reaction with respect to the surface concentration of Ni. Absorption spectra were obtained from kaolinite samples washed with 0.10 M NaNO3 adjusted to pH 3.4 to remove amorphous Al-hydroxide surface deposits or adsorbed Al and from kaolinite that was untreated. For ail samples, EXAFS results revealed the presence of multinuclear Ni surface complexes with a similar, but not identical, local structural environment to pure crystalline Ni(OH)(2). The Ni-Ni bond distances were shorter (3.06-3.11 Angstrom) than in Ni(OH)(2)(s) (3.13 Angstrom) and increased with an increase in surface coverage. Additionally, Al was present in all but the highest surface coverage as a second neighbor backscatterer. At the lower surface coverages (Gamma less than or equal to 0.406 mu mol m(-2)), Al is present at 2.69 Angstrom, indicating the formation of a bidentate Ni surface complex. With increased surface coverage, the d(Ni-Al) increases to 2.96 Angstrom, which is believed to result from a Ni,Al-hydroxide precipitate. No significant structural differences were found between kaolinite pretreatments. Based on these results, a hypothesized mechanism for Ni sorption on kaolinite is proposed.