School of Earth, Atmosphere and Environment, 9 Rainforest Walk, Monash University, Clayton, VIC 3168, Australia.
School of Earth, Atmosphere and Environment, 9 Rainforest Walk, Monash University, Clayton, VIC 3168, Australia.
J Hazard Mater. 2021 May 15;410:124553. doi: 10.1016/j.jhazmat.2020.124553. Epub 2020 Nov 14.
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.
了解通过 U 及其子体衰变衍生的技术增强的天然放射性物质的行为,以及它们随后的分馏、迁移和滞留,对于开发有效的缓解策略和长期放射性风险预测至关重要。在本研究中,多种最先进的、空间分辨的微分析表征技术相结合,系统地跟踪含铀相中的放射性核素(RN)从奥林匹克坝铜浮选精矿中释放和迁移的情况,这些精矿经过硫酸浸出处理。结果突出了含铀矿物(主要是铀矿)的渐进溶解,导致子体 RN 从母体 U 中释放、失衡并最终升级。这与主要的铜-铁-硫化物矿物同时发生,它们与多孔次生铜矿物辉铜矿发生耦合溶解-再沉淀。浸出精矿中剩余的 RN 预算分配在仍存在于原始含铀矿物中的 RN 和被迁移并随后吸附/沉淀到多孔辉铜矿和辅助脉石矿物相(例如重晶石)上的 RN 之间。在进行硫酸浸出之前,对浮选精矿进行进一步研磨会导致先前被包裹在铜-铁-硫化物矿物中的含铀矿物溶解,从而导致子体 RN 的释放和失衡增加,并导致进一步的 RN 升级。影响 RN(迁移、吸附、沉淀)和硫化物矿物(耦合溶解-再沉淀和相关的孔隙生成)的各种过程在水冶回路中连续发生,它们的相互作用控制了 RN 的快速和高度局部化富集。这里开发的工具的创新组合以纳米到厘米尺度详细揭示了水冶处理后矿石中 RN 的不均匀分布和分馏。这种方法为理解 U 及其子体产物在采矿业和能源业中复杂人为和自然过程中的迁移和滞留提供了有效的蓝图。