TL;DR: In this article, the authors report that the dissimilatory iron-reducing bacterium Shewanella alga strain BrY promoted As mobilization from a crystalline ferric arsenate as well as from sorption sites within whole sediments.
Abstract: The mobility of arsenic commonly increases as reducing conditions are established within sediments or flooded soils. Although the reduction of arsenic increases its solubility at circumneutral pH, hydrous ferric oxides (HFO) strongly sorb both As(V) (arsenate) and As(III) (arsenite), the two primary inorganic species. Thus, in the presence of excess HFO, reductive dissolution of iron may be the dominant mechanism by which As is released into solution. In this paper, we report that the dissimilatory iron-reducing bacterium Shewanella alga strain BrY promoted As mobilization from a crystalline ferric arsenate as well as from sorption sites within whole sediments. S. alga cells released arsenate from the mineral scorodite (FeAsO4·2H2O) as a result of dissimilatory (i.e., respiratory) reduction of Fe(III) to Fe(II). Solid-phase analysis with SEM-EDS and XAFS (X-ray absorption fine structure) spectroscopy revealed that the valence states of Fe and As in the solid-phase product were identical to those in soluti...
TL;DR: X-ray absorption fine structure spectroscopy (XAFS) was used to determine arsenic (As) oxidation state, local coordination (to a radius of nearly equal Aa around As), and the relative proportion of different As species in model compounds and three California mine wastes as discussed by the authors.
Abstract: X-ray absorption fine structure spectroscopy (XAFS) was used to determine arsenic (As) oxidation state, local coordination (to a radius of nearly equal Aa around As), and the relative proportion of different As species in model compounds and three California mine wastes: fully oxidized tailings (Ruth Mine), partially oxidized tailings (Argonaut Mine), and roasted sulfide ore (Spenceville Mine). Mineralogy was characterized by Rietveld refinement of X-ray powder diffraction patterns. The spatial distribution of As in the mine wastes (at several micrometers spatial resolution) was determined by electron microprobe analyses. X-ray absorption near edge structure (XANES) analysis indicates that As (super 5+) is the dominant oxidation state in the mine samples, but mixed oxidation states (nominally As 0 and AS (super 5+) ) were observed in the Argonaut Mine waste. Non-linear, least-squares fits of mine waste EXAFS (Extended XAFS) spectra indicate variable As speciation in each of the three mine wastes: As (super 5+) in the Ruth Mine sample is sorbed on ferric oxyhydroxides and aluminosilicates (probably clay) in roughly equal portions. Tailings from the Argonaut Mine contain nearly equal 20% As bound in arsenopyrite (FeAsS) and arsenical pyrite (FeS (sub 2-x) Asx) and nearly equal 80% As (super 5+) in a precipitate such as scorodite (FeAsO 4 .2H 2 O); however, no precipitate was detected by X-ray diffraction or microprobe analysis, suggesting that the phase is poorly crystalline or has low abundance (total As in sample = 262 ppm). Roasted sulfide ore of the Spenceville Mine contains As (super 5+) substituted for sulfate in jarosite [KFe 3 (SO 4 ) 2 (OH) 6 ] or incorporated in the structure of an unidentified Ca- or K-bearing phase, and As (super 5+) sorbed to the surfaces of hematite or ferric oxyhydroxide grains. Determination of solid-phase As speciation in mine wastes by XAFS spectroscopy is a valuable first step in the evaluation of its bioavailability, because the mobility and toxicity of As compounds vary with oxidation state. As bound in precipitates, as in the Argonaut mine sample, is considered to be less available for uptake by organisms than when sorbed on mineral surfaces or coprecipitated with poorly crystalline phases, as found for the Ruth and Spenceville mine wastes.
TL;DR: In this paper, the solubility data for amorphous ferric arsenate and scorodite have been reevaluated using the geochemical code PHREEQC with a modified thermodynamic database for the arsenic species.
TL;DR: In this paper, Fourier transformed infrared (FTIR) spectroscopy was used to characterize arsenate-ferrihydrite sorption solids synthesized at pH 3-8.
TL;DR: In this article, basic ferric arsenates precipitated from hydrometallurgical liquors by hydrolysis are shown to be very insoluble over a range of pHs.