Influence of redox atmospheres on selenate retention by mackinawite, magnetite and pyrite
Year: 2026
Type: article
Abstract: Understanding the redox transformations of selenium (Se) under varying redox atmospheres is critical for predicting its environmental fate and optimizing Se removal from contaminated wastewater. However, the influence of redox atmospheres, specifically H 2 and O 2 , on Se transformation mechanisms and the structural nature of the resulting Se(0) remains poorly understood. In this study, we investigated the interactions between aqueous selenate (Se(VI)) and Fe(II)-bearing minerals (pyrite, magnetite and mackinawite) under N 2 , H 2 and air atmospheres, employing comprehensive characterizations on both aqueous and solid speciation. Our findings reveal that H 2 and air atmospheres could enhance Se removal by pyrite but limit its removal by mackinawite, while magnetite shows no significant atmospheric influence on Se removal. Alongside Se removal, sorbed Se(VI) was transformed into distinct elemental Se depending on the mineral: trigonal γ-Se nanoneedles on magnetite, monoclinic β-Se on mackinawite, and nanosized amorphous Se(0) on pyrite. Moreover, H 2 significantly lowered the solution redox potential, favoring the reduction of sorbed Se(VI) to Se(0) or FeSe x . Overall, this work provides valuable insights for optimizing Se remediation and recovery strategies in Se-contaminated wastewater and improving understanding of Se behavior in diverse geochemical systems, including nuclear waste disposal repositories.
Source: Journal of Hazardous Materials
Institutions: Centre National de la Recherche Scientifique, Geological Survey of Denmark and Greenland, Institut des Sciences de la Terre, Université Grenoble Alpes, Sorbonne Université, Institut de minéralogie, de physique des matériaux et de cosmochimie, Institut de Recherche pour le Développement, ALBA Synchrotron (Spain), Agence Nationale pour la Gestion des Déchets Radioactifs, North China Electric Power University
Language: English
Subfield: Environmental Chemistry
Field: Environmental Science
Domain: Physical Sciences
Open Access status: hybrid
Estimated APC paid: $4,340
Awards: G3738607208, G5477342693
OpenAlex ID: W7140199080
