KINETICS OF ARSENOPYRITE OXIDATIVE DISSOLUTION BY OXYGEN

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dc.contributor.author Walker F.P.
dc.contributor.author Schreiber M.E.
dc.contributor.author Rimstidt J.D.
dc.date.accessioned 2024-05-05T03:46:20Z
dc.date.available 2024-05-05T03:46:20Z
dc.date.issued 2006
dc.identifier https://elibrary.ru/item.asp?id=12091877
dc.identifier.citation Geochimica et Cosmochimica Acta, 2006, 70, 7, 1668-1676
dc.identifier.issn 0016-7037
dc.identifier.uri https://repository.geologyscience.ru/handle/123456789/43845
dc.description.abstract We used a mixed flow reactor system to determine the rate and infer a mechanism for arsenopyrite (FeAsS) oxidation by dissolved oxygen (DO) at 25 °C and circumneutral pH. Results indicate that under circumneutral pH (6.3-6.7), the rate of arsenopyrite oxidation, 10-10.14?0.03 mol m-2 s-1, is essentially independent of DO over the geologically significant range of 0.3-17 mg L-1. Arsenic and sulfur are released from arsenopyrite in an approximate 1:1 molar ratio, suggesting that oxidative dissolution by oxygen under circumneutral pH is congruent. Slower rates of iron release from the reactor indicate that some of the iron is lost from the effluent by oxidation to Fe(III) which subsequently hydrolyzes and precipitates. Using the electrochemical cell model for understanding sulfide oxidation, our results suggest that the rate-determining step in arsenopyrite oxidation is the reduction of water at the anodic site rather than the transfer of electrons from the cathodic site to oxygen as has been suggested for other sulfide minerals such as pyrite. ? 2005 Elsevier Inc. All rights reserved.
dc.subject ARSENOPYRITE
dc.subject DISSOLUTION
dc.subject OXIDATION
dc.subject REACTION KINETICS
dc.title KINETICS OF ARSENOPYRITE OXIDATIVE DISSOLUTION BY OXYGEN
dc.type Статья
dc.identifier.doi 10.1016/j.gca.2005.12.010


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