Understanding the mobility and retention of uranium and its daughter products.

Disequilibrium Fractionation Radionuclides TENORM U-decay chain

Journal

Journal of hazardous materials
ISSN: 1873-3336
Titre abrégé: J Hazard Mater
Pays: Netherlands
ID NLM: 9422688

Informations de publication

Date de publication:
15 05 2021
Historique:
received: 08 09 2020
revised: 07 11 2020
accepted: 10 11 2020
pubmed: 24 11 2020
medline: 24 11 2020
entrez: 23 11 2020
Statut: ppublish

Résumé

Knowledge of the behavior of technologically enhanced naturally occurring radioactive materials derived through the decay of U and its daughter products, and their subsequent fractionation, mobilization and retention, is essential to develop effective mitigation strategies and long-term radiological risk prediction. In the present study, multiple state-of-the-art, spatially resolved micro-analytical characterization techniques were combined to systematically track the liberation and migration of radionuclides (RN) from U-bearing phases in an Olympic Dam Cu flotation concentrate following sulfuric-acid-leach processing. The results highlighted the progressive dissolution of U-bearing minerals (mainly uraninite) leading to the release, disequilibrium and ultimately upgrade of daughter RN from the parent U. This occurred in conjunction with primary Cu-Fe-sulfide minerals undergoing coupled-dissolution reprecipitation to the porous secondary Cu-mineral, covellite. The budget of RN remaining in the leached concentrate was split between RN still hosted in the original U-bearing minerals, and RN that were mobilized and subsequently sorbed/precipitated onto porous covellite and auxiliary gangue mineral phases (e.g. barite). Further grinding of the flotation concentrate prior to sulfuric-acid-leach led to dissolution of U-bearing minerals previously encapsulated within Cu-Fe-sulfide minerals, resulting in increased release and disequilibrium of daughter RN, and causing further RN upgrade. The various processes that affect RN (mobility, sorption, precipitation) and sulfide minerals (coupled-dissolution reprecipitation and associated porosity generation) occur continuously within the hydrometallurgical circuit, and their interplay controls the rapid and highly localized enrichment of RN. The innovative combination of tools developed here reveal the heterogeneous distribution and fractionation of the RN in the ores following hydrometallurgical treatment at nm to cm-scales in exquisite detail. This approach provides an effective blueprint for understanding of the mobility and retention of U and its daughter products in complex anthropogenic and natural processes in the mining and energy industries.

Identifiants

pubmed: 33223312
pii: S0304-3894(20)32543-7
doi: 10.1016/j.jhazmat.2020.124553
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

124553

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Auteurs

Rahul Ram (R)

School of Earth, Atmosphere and Environment, 9 Rainforest Walk, Monash University, Clayton, VIC 3168, Australia. Electronic address: rahul.ram@monash.edu.

Nicholas D Owen (ND)

School of Earth, Atmosphere and Environment, 9 Rainforest Walk, Monash University, Clayton, VIC 3168, Australia.

Chris Kalnins (C)

Institute for Photonics and Advanced Sensing and School of Physical Sciences, University of Adelaide, Adelaide, SA, Australia.

Nigel J Cook (NJ)

School of Civil, Environmental and Mining Engineering, The University of Adelaide, SA 5005, Australia.

Kathy Ehrig (K)

BHP Olympic Dam, Adelaide, SA 5000, Australia.

Barbara Etschmann (B)

School of Earth, Atmosphere and Environment, 9 Rainforest Walk, Monash University, Clayton, VIC 3168, Australia.

Mark Rollog (M)

School of Civil, Environmental and Mining Engineering, The University of Adelaide, SA 5005, Australia.

Weng Fu (W)

School of Chemical Engineering, The University of Queensland, Level 3, Chemical Engineering Building (74), St Lucia, QLD 4072, Australia.

James Vaughan (J)

School of Chemical Engineering, The University of Queensland, Level 3, Chemical Engineering Building (74), St Lucia, QLD 4072, Australia.

Allan Pring (A)

College of Science and Engineering, Flinders University, Bedford Park, SA 5042, Australia.

Mark I Pownceby (MI)

CSIRO Mineral Resources, Clayton 3173, Australia.

Nigel Spooner (N)

Institute for Photonics and Advanced Sensing and School of Physical Sciences, University of Adelaide, Adelaide, SA, Australia.

Ruth Shaw (R)

Institute for Photonics and Advanced Sensing and School of Physical Sciences, University of Adelaide, Adelaide, SA, Australia.

Daryl Howard (D)

Australian Synchrotron, 800 Blackburn Road, Clayton, VIC 3168, Australia.

Anthony M Hooker (AM)

Institute for Photonics and Advanced Sensing and School of Physical Sciences, University of Adelaide, Adelaide, SA, Australia.

David Ottaway (D)

Institute for Photonics and Advanced Sensing and School of Physical Sciences, University of Adelaide, Adelaide, SA, Australia.

Danielle Questiaux (D)

Institute for Photonics and Advanced Sensing and School of Physical Sciences, University of Adelaide, Adelaide, SA, Australia.

Joël Brugger (J)

School of Earth, Atmosphere and Environment, 9 Rainforest Walk, Monash University, Clayton, VIC 3168, Australia. Electronic address: joel.brugger@monash.edu.

Classifications MeSH