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碳酸盐岩风化和成土过程中铀和钍的地球化学行为:形态分析的制约。

Geochemical behaviors of uranium and thorium during weathering and pedogenesis of carbonate rock: constraint from their speciation.

机构信息

School of Resource Environment and Safety Engineering, University of South China, 421001, Hengyang, China.

Hunan Key Laboratory of Rare Metal Minerals Exploitation and Geological Disposal of Wastes, University of South China, 421001, Hengyang, China.

出版信息

Environ Sci Pollut Res Int. 2023 Sep;30(42):95348-95366. doi: 10.1007/s11356-023-29007-5. Epub 2023 Aug 7.

Abstract

During weathering and pedogenesis of carbonate rock with poor-uranium (U) and thorium (Th), U and Th present the characteristics of strong leaching (especially U) and significant residual enrichment, the cause of which is still unclear. In this paper, a weathering profile developed by dolomite in karst area of Guizhou province in southwest China was selected, which showed zonation characteristics of bedrock (Y), powdery rock (Yf), and soil layer (T1 to T12) from the bottom to up. Through the determination of the occurrence speciation of U and Th in Y and weathering profile, combined with mineralogical, geochemical characteristics, and element mass balance calculation, the constraints of U and Th speciation on the geochemical behavior of U and Th during the weathering of carbonate rock were revealed. The results proved that U and Th in Y preferentially existed in acid insoluble phase, for example, the contents of U and Th in Y were 0.90 mg·kg and 0.28 mg·kg, respectively, while those in acid insoluble matter were 2.34 mg·kg and 2.57 mg·kg, respectively, but because the mass percentage of acid insoluble matter was extremely low (0.95%), the mass percentages of U and Th in the acid soluble phase in the whole rock were absolutely superior (96% of U and 86% Th). The U and Th in the acid soluble phase of Y were mainly adsorbed on the crystal surface of carbonate minerals or existed in the cement, and the U and Th in the carbonate lattice only accounted for a small proportion. From Y to Yf with the initial dissolution, U and Th released from the surface of carbonate minerals and cements were in carbonate-rich alkaline environment, and these portions of U and Th were leached out, resulting in strong loss of U and Th in the Yf (the loss rates are 83% of U and 65% of Th, respectively). From the Yf to the overlying soil layer T1, the carbonate components were completely dissolved, and the U and Th released from the carbonate lattice showed different behaviors, where U was completely leached and Th tended to stay in the weathered residue. Thus, in the soil layer T1 formed by Y or Yf , the residual U was the inheritance of the U in the acid insoluble phase of Y; For Th, it not only inherited the Th of acid insoluble phase of Y, but also superimposed the Th from carbonate lattice in Y. On the other hand, during the evolution process from Y to Yf and to soil layer T1, with the dissolution of carbonate, the acid insoluble phase also showed a significant tendency of chemical weathering. However, the U and Th in the Y acid insoluble phase were not leached with the decomposition of the acid insoluble phase but were redistributed among the residual phases. For the geochemical behaviors of U and Th in the evolution of soil profile (T1~T12), they were subjected to the occurrence speciation of U and Th in T1 and the change of U and Th occurrence speciation with the upward direction of soil profile. The U and Th released from the carrier minerals were mainly redistributed among the residual solid phases, which weakened the intensity of their further loss. This study deepens the understanding of the geochemical behavior of radionuclides in karst environment and provides reference for the treatment of radioactive pollution in karst areas.

摘要

在碳酸盐岩风化和成土过程中,铀(U)和钍(Th)的含量较低,铀和钍表现出强烈淋失(特别是铀)和显著残留富集的特征,其原因尚不清楚。本文选取中国西南部贵州省碳酸盐岩喀斯特地区发育的风化剖面,从底部到顶部依次表现为基岩(Y)、粉状岩(Yf)和土壤层(T1 到 T12)的分带特征。通过对 Y 和风化剖面中 U 和 Th 的赋存形态的测定,结合矿物学、地球化学特征和元素质量平衡计算,揭示了 U 和 Th 形态对碳酸盐岩风化过程中 U 和 Th 地球化学行为的制约。结果表明,Y 中的 U 和 Th 优先存在于酸不溶相中,例如,Y 中的 U 和 Th 含量分别为 0.90mg·kg 和 0.28mg·kg,而酸不溶物中的 U 和 Th 含量分别为 2.34mg·kg 和 2.57mg·kg,但是由于酸不溶物的质量百分比极低(0.95%),因此在全岩中酸可溶相中的 U 和 Th 的质量百分比绝对占优势(U 占 96%,Th 占 86%)。Y 中酸可溶相中的 U 和 Th 主要吸附在碳酸盐矿物的晶面上或存在于胶结物中,而在碳酸盐晶格中的 U 和 Th 仅占很小的比例。从 Y 到初始溶解的 Yf,从碳酸盐矿物和胶结物表面释放出的 U 和 Th 处于富含碳酸盐的碱性环境中,这些部分的 U 和 Th 被淋滤出来,导致 Yf 中 U 和 Th 的强烈损失(U 的损失率为 83%,Th 的损失率为 65%)。从 Yf 到上覆土壤层 T1,碳酸盐成分完全溶解,从碳酸盐晶格中释放出的 U 和 Th 表现出不同的行为,其中 U 完全淋滤,Th 倾向于留在风化残余物中。因此,在由 Y 或 Yf 形成的土壤层 T1 中,残留的 U 是 Y 中酸不溶相 U 的继承;对于 Th,它不仅继承了 Y 中酸不溶相的 Th,而且还叠加了 Y 中碳酸盐晶格中的 Th。另一方面,在 Y 向 Yf 和土壤层 T1 的演化过程中,随着碳酸盐的溶解,酸不溶相也表现出明显的化学风化趋势。然而,Y 中酸不溶相中的 U 和 Th 并没有随着酸不溶相的分解而被淋滤,而是在残留相中重新分配。对于土壤剖面演化过程(T1~T12)中 U 和 Th 的地球化学行为,它们受到 T1 中 U 和 Th 赋存形态的影响以及 U 和 Th 赋存形态随土壤剖面向上方向的变化。从载体矿物中释放出的 U 和 Th 主要在残留固相之间重新分配,这削弱了它们进一步损失的强度。本研究深化了对喀斯特环境中放射性核素地球化学行为的认识,为喀斯特地区放射性污染的治理提供了参考。

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