School of Environmental Science and Engineering, Sun Yat-sen University, Guangzhou 510275, China; Guangdong Provincial Key Laboratory of Environmental Pollution Control and Remediation Technology, Guangzhou, China; Guangdong Provincial Engineering Research Center for Heavy Metal Contaminated Soil Remediation, Sun Yat-sen University, Guangzhou, PR China.
School of Environmental Science and Engineering, Sun Yat-sen University, Guangzhou 510275, China; Guangdong Provincial Key Laboratory of Environmental Pollution Control and Remediation Technology, Guangzhou, China; Guangdong Provincial Engineering Research Center for Heavy Metal Contaminated Soil Remediation, Sun Yat-sen University, Guangzhou, PR China.
Water Res. 2024 Jun 1;256:121582. doi: 10.1016/j.watres.2024.121582. Epub 2024 Apr 7.
Ion-adsorption rare earth element (REE) deposits distributed in the subtropics provide a rich global source of REEs, but in situ injection of REEs extractant into the mine can result in leachate being leaked into the surrounding groundwater systems. Due to the lack of understanding of REE speciation distribution, particularly colloidal characteristics in a mining area, the risks of REEs migration caused by in situ leaching of ion-adsorption REE deposits has not been concerned. Here, ultrafiltration and asymmetric flow field-flow fractionation coupled with inductively coupled plasma mass spectrometry (AF4-ICP-MS) were integrated to characterize the size and composition of REEs in leachate and groundwater from mining catchments in South China. Results show that REEs were associated with four fractions: 1) the <1 kDa fraction including dissolved REEs; 2) the 1 - 100 kDa nano-colloidal fraction containing organic compounds; 3) the 100 kDa - 220 nm fine colloids including organic-mineral (Fe, Mn and Al (oxy)hydroxides and clay minerals); 4) the >220 nm coarse colloids and acid soluble particles (ASPs) comprising minerals. Influenced by the ion exchange effect of in situ leaching, REEs in leachate were mostly dissolved (79 %). The pH of the groundwater far from the mine site was increased (5.8 - 7.3), the fine organic-mineral colloids (46 % - 80 %) were the main vectors of transport for REEs. Further analysis by AF4 revealed that the fine colloids can be divided into mineral-rich (F1, 100 kDa - 120 nm) and organic matter-rich (F2, 120 - 220 nm) populations. The main colloids associated with REEs shifted from F1 (64 % ∼ 76 %) to F2 (50 % ∼ 52 %) away from the mining area. For F1 and F2, the metal/C molar ratio decreased away from the mining area and middle to heavy REE enrichment was presented. According to the REE fractionation, organic matter was the predominant component capable of binding REEs in fine colloids. Overall, our results indicate that REEs in the groundwater system shifted from the dissolved to the colloidal phase in a catchment affected by in situ leaching, and organic-mineral colloids play an important role in facilitating the migration of REEs.
分布在亚热带地区的离子吸附型稀土元素 (REE) 矿床为全球 REE 提供了丰富的资源,但将 REE 萃取剂原位注入矿山会导致浸出液泄漏到周围地下水系统中。由于对 REE 形态分布,特别是矿区胶体特性缺乏了解,因此尚未关注离子吸附型 REE 矿床原位浸出引起的 REE 迁移风险。在这里,超滤和不对称流场流分级结合电感耦合等离子体质谱(AF4-ICP-MS)被整合来描述中国南方矿区集水区浸出液和地下水中 REE 的大小和组成。结果表明,REE 与四个部分相关联:1)<1 kDa 部分包括溶解的 REE;2)1 - 100 kDa 纳米胶体部分包含有机化合物;3)100 kDa - 220 nm 细胶体包括有机-矿物(Fe、Mn 和 Al(氢)氧化物和粘土矿物);4)>220 nm 粗胶体和酸可溶颗粒(ASPs)包括矿物。受原地浸出离子交换作用的影响,浸出液中的 REE 主要以溶解态存在(79%)。远离矿山场地的地下水的 pH 值增加(5.8 - 7.3),细有机-矿物胶体(46% - 80%)是 REE 迁移的主要载体。通过 AF4 的进一步分析表明,细胶体可以分为富含矿物(F1,100 kDa - 120 nm)和富含有机物(F2,120 - 220 nm)两种类型。与 REE 相关的主要胶体从矿区(64%∼76%)向远离矿区(50%∼52%)的 F2 转移。对于 F1 和 F2,远离矿区的金属/C 摩尔比降低,并且中重 REE 发生了富集。根据 REE 分馏,有机物是在原地浸出影响的集水区中结合 REE 的主要胶体成分。总的来说,我们的结果表明,在受原位浸出影响的集水区中,地下水中的 REE 从溶解相转移到胶体相,有机-矿物胶体在促进 REE 迁移方面发挥了重要作用。