Studies of equilibrium, structure, and dynamics in the aqueous Al(III)-oxalate-fluoride system by potentiometry, 13C and 19F NMR spectroscopy

Andrea Bodor, Imte Tóth, Istudor Bányai, László Zékány, Staffan Sjöberg

Research output: Article

8 Citations (Scopus)

Abstract

The AlOx1-3 (Ox = oxalate) species were identified in 0.6 M aqueous NaCl by 13C nuclear magnetic resonance (NMR). Rate constants and activation parameters for intramolecular cis/trans isomerization of the Werner-type AlOx-2 complex (k(298 K) = 5 s-1, ΔH# = 67 ± 5 kJ mol-1, ΔS# = -6 ± 6 J mol-1 K-1, the rate determining step could be the breaking of the Al-O(C=O) bond) and a very slow intermolecular ligand exchange reaction of AlOx3-3 complex and the free ligand (k30(298 K) = 6.6 · 10-5 s-1, ΔH# = 164 ± 17 kJ mol-1, ΔS# = 225 ± 51 J mol-1 K-1, D/Id mechanism) were determined by dynamic 1D and 2D 13C NMR measurements. Mixed complexes, AlFOx, AlFOx2-2, AlF2 Ox-, and AlF2Ox3-2, with overall stability (logβ) of 11.53 ± 0.03, 15.67 ± 0.03, 15.74 ± 0.02, and 19.10 ± 0.04 were measured by potentiometry using pH- and fluoride-selective electrodes and confirmed by 13C and19F NMR. The role of these complexes in gibbsite dissolution was modeled. The mixed Al(III)-Ox2--F- complexes have to be considered as the chemical speciation of Al(III) in natural waters is discussed.

Original languageEnglish
Pages (from-to)2793-2803
Number of pages11
JournalGeochimica et Cosmochimica Acta
Volume67
Issue number15
DOIs
Publication statusPublished - aug. 1 2003

ASJC Scopus subject areas

  • Geochemistry and Petrology

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