Environmental Science & Technology · 2002 · 415 citations · 16 references
Natural SciencesChemistryEarth SciencesGeochemistryInorganic ChemistryMineralogyAcid Mine DrainageAmorphous Soil MineralsIron OxidesMineral GenesisMineral GeochemistryAcid Mine Drainage GeochemistryGoethite FormationHyperfine Field DeterminationIron GeochemistryMagnetic Dipole Hyperfine InteractionMagnetic Hyperfine SplittingPh StabilityX-ray Diffraction Analysis
Ochreous precipitates containing 5.5-69.8 g/kg As were isolated from mine drainage in Finland and were composed of schwertmannite, ferrihydrite, and goethite. Schwertmannite formation was favored at pH 3-4, but its structure was degraded at high As levels. A series of coprecipitates were therefore prepared from mixed iron arsenate/sulfate solutions to define the limits of schwertmannite stability. Schwertmannite was replaced as the dominant phase by a poorly crystalline ironIII hydroxy arsenate (FeOHAs) when As/Fe mole ratios exceeded 0.15. The FeOHAs gave an X-ray diffraction pattern similar to that obtained from an "amorphous" ironIII arsenate (As/Fe = 1.0) with broad peaks at 0.30 and 0.16 nm. The FeOHAs possessed a magnetic hyperfinefield of 41.9T at 4.2 K that was intermediate to those of schwertmannite (46.1 T) and the ironIII arsenate (24.8 T). These data indicate a strong disruptive effect of arsenate on magnetic ordering and structure development in schwertmannite. Equilibration of 0.01 M arsenate solutions with freshly prepared schwertmannite and 2-line ferrihydrite at pH 3.0 for up to 60 d gave sorbed As contents of 175 and 210 g/kg, respectively. Arsenate sorption degraded the host schwertmannite and ferrihydrite, perhaps due to the formation of an FeOHAs surface phase.
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Annette M. Olivarez, Robert M. Owen · Geochimica et Cosmochimica Acta · 1990 · 1.1K citations
Solubilities and stabilities of ferric arsenate compounds
E. Krause, V. Ettel · Hydrometallurgy · 1989 · 264 citations