School of Environmental Science and Engineering, Guangzhou University; Key Laboratory of Water Quality and Conservation in the Pearl River Delta, Ministry of Education, Guangzhou 510006, China; Guangdong Provincial Key Laboratory of Radionuclides Pollution Control and Resources, Guangzhou 510006, China.
School of Environmental Science and Engineering, Guangzhou University; Key Laboratory of Water Quality and Conservation in the Pearl River Delta, Ministry of Education, Guangzhou 510006, China.
J Hazard Mater. 2021 Jul 15;414:125466. doi: 10.1016/j.jhazmat.2021.125466. Epub 2021 Feb 19.
Uranium (U) geochemistry and its isotopic compositions of reservoir sediments in U mine area were poorly understood. Herein, U and Th isotopic compositions were employed to investigate source apportionment and geochemical behavior of U in 41 reservoir sediments from a U mining area, Guangdong, China. The remarkably high contents of both total U (207.3-1117.7 mg/kg) and acid-leachable U (90.3-638.5 mg/kg) in the sediments exhibit a severe U contamination and mobilization-release risk. The U/Th activity ratios (ARs) indicate that all sediments have been contaminated apparently by U as a result of discharge of U containing wastewater, especially uranium mill tailings (UMT) leachate, while the variations of U/Th ARs are dominated by U geochemical behaviors (mainly redox process and adsorption). The U isotopic compositions (δU) showed a large variance through the sediment profile, varying from - 0.62 to - 0.04‰. The relation between δU and acid-leachable U fraction demonstrates that the U isotopic fractionation in sediments can be controlled by bedrock weathering (natural activity), UMT leachate (anthropogenic activity) and subsequent biogeochemical processes. The findings suggest that U-Th isotopes are a powerful tool to better understand U geochemical processes and enrichment mechanism in sediments that were affected by combined sources and driving forces.
矿区储层沉积物中铀(U)的地球化学及其同位素组成研究还不够深入。本研究采用 U 和 Th 同位素组成来探讨中国广东某铀矿区 41 个储层沉积物中 U 的来源分配和地球化学行为。沉积物中总 U(207.3-1117.7 mg/kg)和酸可提取 U(90.3-638.5 mg/kg)的含量均很高,表明存在严重的 U 污染和迁移释放风险。U/Th 活度比(AR)表明,所有沉积物均受到 U 的明显污染,这是由于含 U 废水(特别是铀尾矿库浸出液)的排放所致,而 U/Th AR 的变化主要受 U 的地球化学行为(主要是氧化还原过程和吸附)控制。U 同位素组成(δU)在整个沉积剖面中变化较大,范围为-0.62 至-0.04‰。δU 与酸可提取 U 分数之间的关系表明,沉积物中 U 同位素分馏可受基岩风化(自然活动)、铀尾矿库浸出液(人为活动)和随后的生物地球化学过程控制。研究结果表明,U-Th 同位素是更好地理解受多种来源和驱动力影响的沉积物中 U 地球化学过程和富集机制的有力工具。