4.7 Article

Reductive immobilization of 99Tc(VII) by FeS2: The effect of marcasite

Journal

CHEMOSPHERE
Volume 281, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2021.130904

Keywords

Technetium removal; Iron sulfide; Iron sulfate; Pyrite; Remediation

Funding

  1. German Federal Ministry of Economic Affairs and Energy (VESPA II joint project) [02E11607B]

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The study investigated the reductive immobilization of Tc-99 using a synthetic FeS2 mixture, finding complete removal of Tc at certain pH levels and revealing the oxidation of S2- to SO42- by marcasite as a key mechanism for Tc immobilization. The research provides new insights into the redox reactions involved in Tc(VII) mobilization and highlights the potential of marcasite for natural Tc remediation by delaying re-oxidation of Tc(IV).
Reductive immobilization of Tc-99 by a synthetic FeS2 mixture, i.e. marcasite-pyrite 60:40, was studied by a combined approach of batch experiments and powder X-ray diffraction, X-ray photoelectron spectroscopy as well as Raman microscopy. It was found that the FeS2 mixture removes 100% of Tc from the suspension after 7 days in contact at 6.0 < pH <= 9.0. The retention outside that pH range was slower and incomplete. Spectroscopic analysis showed that the redox active species at pH 6.0 is Fe2+ as expected from previous works with pyrite. However, at pH 10.0 the surprising oxidation of S2- to SO42- was found responsible for Tc immobilization. This was explained by the high reactivity of marcasite that is easily oxidized to produce H2SO4. Our work provides new molecular insights into the reductive mobilization of Tc(VII) by oxidative formation of sulfate. The assigned molecular reactions may also be relevant for the assessment of other redox reactive contaminants. Technetium re-oxidation experiments showed that the fast oxidation of marcasite is associated to the reduction of the remaining Tc(VII) in solution, which gives marcasite the potential of Tc natural remediation since it delays the re-oxidation of Tc(IV).

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