Dalton Transactions · 2005 · 52 citations · 21 references
Natural SciencesBiochemistryChemistryAnalytical ChemistryChemical KineticsInorganic ChemistryAcid-base ChemistryAluminum HydroxidesElemental SpeciationDynamic Nmr SpectroscopyHydrolysisHydrolysis ReactionsKinetic Data AnalysisMetal Ion SpeciationSpeciation AnalysisSpeciation KineticsSpeciation Processes
Speciation diagrams of aluminium ions in aqueous solution (0.2 M) at high temperature (90 degrees C) have been obtained from 48 h time-resolved multi-batch titration experiments monitored by 27Al NMR spectroscopy, potentiometry and dynamic light scattering. The quantitative speciation patterns and kinetic data obtained offer a dynamic picture of the distribution of soluble and insoluble Al species as a function of hydrolysis ratio h(h=[OH-]/[Al3+]) over a very broad range of conditions (-1.0 < or =h < or = 4.0). Monomeric, small oligomeric, tridecameric (the 'Al13-mer') and the recently characterised 30-meric aluminium species (the 'Al30-mer') as well as aluminium hydroxide have been identified and quantified. The Al13-mer species dominates over a relatively broad range of hydrolysis ratios (1.5 < or =h< or = 2.7) during the first 6 h of experiment, but are gradually replaced by Al30-mers at longer reaction times. Kinetic profiles indicate that the formation of the Al30-mer is limited by the disappearance of the Al13 species at mildly acidic conditions. The estimated rate constants of both hydrolytic processes show good internal correlation at h> or = 1.5. The effect of local perturbations leading to the formation of aluminium hydroxide below the electroneutrality point (h= 3.0) has been estimated quantitatively.
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Jesse L. C. Rowsell, Linda F. Nazar · Journal of the American Chemical Society · 2000 · 178 citations