Arsenic binding to organic and inorganic sulfur species during microbial sulfate reduction: a sediment flow-through reactor experiment - Archive ouverte HAL Accéder directement au contenu
Article Dans Une Revue Environmental Chemistry Année : 2013

Arsenic binding to organic and inorganic sulfur species during microbial sulfate reduction: a sediment flow-through reactor experiment

Résumé

Flow-through reactors (FTRs) were used to assess the mobility of arsenic under sulfate reducing conditions in natural, undisturbed lake sediments. The sediment slices in the FTRs were supplied continuously with inflow solutions containing sulfate and soluble As-III or As-V and, after 3 weeks, also lactate. The experiment ran for a total of 8 weeks. The dissolved iron concentration, pH, redox potential (E-h), as well as aqueous As and sulfur speciation were monitored in the outflow solutions. In FTRs containing surface sediment enriched in labile organic matter (OM), microbial sulfate reduction led to an accumulation of organically bound S, as evidenced by X-ray absorption spectroscopy. For these FTRs, the inflowing dissolved As concentration of 20 mu M was lowered by two orders of magnitude, producing outflow concentrations of 0.2 mu M monothioarsenate and 0.1 mu M arsenite. In FTRs containing sediment collected at greater depth, sulfide and zero-valent S precipitated as pyrite and elemental S, while steady-state outflow arsenite concentrations remained near 5 mu M. The observations thus suggest that As sequestration is enhanced when sediment OM buffers the free sulfide and zero-valent S concentrations. An updated conceptual model for the fate of As in the anoxic As-C-S-Fe system is presented based on the results of this study.

Dates et versions

hal-01426271 , version 1 (04-01-2017)

Identifiants

Citer

Raoul-Marie Couture, Dirk Wallschlaeger, Jérôme Rose, Philippe van Cappellen. Arsenic binding to organic and inorganic sulfur species during microbial sulfate reduction: a sediment flow-through reactor experiment. Environmental Chemistry, 2013, 10 (4), pp.285-294. ⟨10.1071/EN13010⟩. ⟨hal-01426271⟩
130 Consultations
0 Téléchargements

Altmetric

Partager

Gmail Facebook X LinkedIn More