Behavior and mechanism of different fraction lead leach with several typical sulfate lixiviants in the weathered crust elution-deposited rare earth ore.

Recently, some new leaching agents without ammonium, such as magnesium sulfate (MgSO4) and aluminum sulfate [Al2(SO4)3], have been developed to eliminate ammonia nitrogen pollution in in situ mining process of the weathered crust elution-deposited rare earth ore (WCED-REO), but they might cause heavy metal contamination. In this study, characteristics and mechanisms of different fractions of lead (Pb) released by (NH4)2SO4, MgSO4 and Al2(SO4)3 leaching agents were investigated using batch experiments and column leaching tests. The experimental results showed that the amounts of Pb released by the different leaching agents followed the trend of Al2(SO4)3 > (NH4)2SO4 > MgSO4 under the same total cationic charge, and both the acid extractable and reducible fractions of Pb were released. The release of acid extractable fraction Pb was related to the cation hydration radius of NH4+, Mg2+, and Al3+, whereas the release of reducible fraction Pb was mainly influenced by the concentration of H+, especially at pH < 4.0. Furthermore, column leaching tests indicated that pH has little effect on the Pb contents of different fractions released by (NH4)2SO4 and MgSO4 in leaching the WCED-REO. Although Al2(SO4)3 released the largest contents of rare earth and Pb in leachate, the content of residual acid extractable fraction Pb in soil was the most after water injection (simulating the cleaning process after mining). This work can provide a scientific method and theoretical basis for comprehensively assessing the environmental impact of new leaching agents on WCED-REO mining.

The influence of soil particle size distribution and clay minerals on ammonium nitrogen in weathered crust elution-deposited rare earth tailing.

Even after being abandoned for many years, a large number of weathered crust elution-deposited rare earth (WCED-RE) tailings continue to release ammonia nitrogen (AN) pollution into their surrounding environments. However, the influences of particle size distribution and clay minerals on AN pollution caused by these tailings have been insufficiently studied, and its causes are poorly understood. In this study, soil samples at different depths (5, 7, 9, 11 and 14 m) were collected from a rare earth tailing in Ganzhou City, Jiangxi Province, China. Particles were screened by size into six groups (2-1, 1-0.5, 0.5-0.25, 0.25-0.1, 0.1-0.075 and < 0.075 mm), and AN forms were extracted. The results showed that as soil particle size decreases, both soil specific surface area and clay content increase, leading to stronger AN enrichment ability. With increased sampling depth, the distribution of clay across the six particle fractions became more uniform, such that the accumulation of AN in soil with fine particle size was less obvious. Clay minerals with different capacities for AN enrichment vary with sampling depth. This variation is responsible for the profile of AN distribution in the mine, where AN first increases and then decreases as vertical depth is increased. Although AN content was highest at 11 m, water soluble AN content was higher in the upper part of the completely weathered layer (5 and 7 m), which poses a higher environmental risk. This study provides significant information to deepen our understanding of the distribution characteristics of AN and its main influencing factors, as well as a foundation for the prevention and remediation of nitrogen pollution from WCED-RE tailings.

Study on Pb release by several new lixiviants in weathered crust elution-deposited rare earth ore leaching process: Behavior and mechanism.

New leaching agents could lead to a reduction in ammonia nitrogen pollution and the supplementation of soil nutrients during in-situ mining. They could also result in the release of even more toxic heavy metals, which has an impact on the environment as well as human health. In this study, column leaching experiments were used to simulate in-situ leaching, and the leaching behavior and fractional changes of lead in weathered crust elution-deposited rare earth ore by different leaching agents were studied. The experimental results showed that the amount of lead that was leached followed the order of CLA (60% CaCl2 + 25% NH4Cl + 15% MgSO4) > (NH4)2SO4 > MgSO4. The lead leaching process was comprised of both an acceleration and deceleration stage that followed the first order kinetic model. The amount of Pb when using compound agent was the greatest most likely because of the presence of Cl-. The soil heavy metal morphology test showed that the three leaching agents primarily leached acid extractable lead, and the compound leaching agent leached the greatest amount of acid extractable Pb, which mainly due to the presence of NH4Cl. The reducible fraction was enriched in the direction of migration of the leachate, which was due to the presence of SO42-. These results indicate that the introduction of leaching agents during the mining process pose a greater risk for the release of heavy metals and provide a theoretical basis for the prevention and remediation of heavy metal pollution in mining areas where new leaching agents were used.

Leach of the weathering crust elution-deposited rare earth ore for low environmental pollution with a combination of (NH4)2SO4 and EDTA.

High concentration of ammonium sulfate, a typical leaching agent, was often used in the mining process of the weathering crust elution-deposited rare earth ore. After mining, a lot of ammonia nitrogen and labile heavy metal fractions were residual in tailings, which may result in a huge potential risk to the environment. In this study, in order to achieve the maximum extraction of rare earth elements and reduce the labile heavy metal, extraction effect and fraction changes of lanthanum (La) and lead (Pb) in the weathering crust elution-deposited rare earth ore were studied by using a compound agent of (NH4)2SO4-EDTA. The extraction efficiency of La was more than 90% by using 0.2% (NH4)2SO4-0.005 M EDTA, which was almost same with that by using 2.0% (NH4)2SO4 solution. In contrast, the extraction efficiency of Pb was 62.3% when use 0.2% (NH4)2SO4-0.005 M EDTA, which is much higher than that (16.16%) achieved by using 2.0% (NH4)2SO4 solution. The released Pb fractions were mainly acid extractable and reducible fractions, and the content of reducible fraction being leached accounted for 70.45% of the total reducible fraction. Therefore, the use of 0.2% (NH4)2SO4-0.005 M EDTA can not only reduce the amount of (NH4)2SO4, but also decrease the labile heavy metal residues in soil, which provides a new way for efficient La extraction with effective preventing and controlling environmental pollution in the process of mining the weathering crust elution-deposited rare earth ore.