Potential protonation sites in the Al_2SiO_5 polymorphs based on polarized FTIR spectroscopy and properties of the electron density distribution

Abstract

Potential protonation sites for, kyanite, sillimanite, and andalusite, located in a mapping of the (3, −3) critical points displayed by their L(r) = −∇^(2)ρ(r) distributions, are compared with polarized single-crystal FTIR spectra of kyanite and sillimanite determined earlier and with andalusite measured in this study. For andalusite, seven peaks were observed when the electric vector, E, is parallel to [100]: four intense ones at 3,440, 3,460, 3,526, and 3,597 cm^(−1) and three weaker ones at 3,480, 3,520, and 3,653 cm−1. Six peaks, three intense ones at 3,440, 3,460, and 3,526 cm^(−1) and three weaker ones at 3,480, 3,520, and 3,653 cm^(−1) when E parallels [010]. No peaks were observed when E is parallel to [001]. The concentration of water in andalusite varies between 110 and 168 ppm by weight % H2O. Polarized FTIR spectra indicate that the OH vector is parallel to (001) in andalusite and sillimanite and (11\ifmmode\expandafter\elseˉ\expandafter\=\fi1) in kyanite. Examination of the L(r) (3, −3) critical points in comparison with the polarized FTIR indicates that H prefers to bond to the oxygen atoms O1 and O2 in andalusite and O2 and O4 in sillimanite which correspond to the underbonded oxygen atoms and those with the largest L(r) maxima. In kyanite, comparison of the FTIR spectrum and the critical points indicates that H will preferentially bond to the two 4-coordinated O2 and O6 atoms.

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