Abstract

Acid rain has long been a great concern because of environmental and ecological problems; however, the effect of acid rain on soil acidification, loss of rare earth elements (REEs) via the leaching process, and transformation are rarely reported in rare earth mining areas. Through a simulated acid rain leaching experience, the effect of acid rain was studied on soil acidification and REEs leaching loss. The results showed that the tested soil had certain buffering capacity against nearly neutral rainwater. However, simulated acid rain of low and very low pH (pH ≤ 3.5) had a greater impact on soil acidification. After eluviating by simulated acid rain of pH 3.5 for 36 h, the pH of tailings, garden soil, paddy soil, and alluvial soil decreased by 20.41, 32.03, 13.60, 16.88, and 15.83 %, respectively, from the original values. For simulated acid rain of pH 2.5, it was 31.89, 44.76, 31.26, 29.87, and 29.15 %, respectively. After simulated acid rain eluviations of low and very low pH (pH ≤ 3.5), the order of the leaching rate of REEs in the tested soil was as follows: garden soil > tailings > paddy soil > alluvial soil. For nearly neutral rainwater (pH 4.5 simulated acid rain and pH 5.6 deionized water), the order was tailings > garden soil > paddy soil > alluvial soil. For simulated acid rain of the same pH, the leaching amounts of REEs in tailings and garden soil were higher than those in paddy soil and alluvial soil. After leaching by low and very low pH-simulated acid rain (pH ≤ 3.5), the peak value of the leaching amount of REEs in all tested soil appeared at 2 h, and then gradually reduced and reached a stable leaching state 20 h after leaching. On leaching by simulated acid rain of pH 2.5, the maximum REEs contents of leachate in tailings, garden soil, paddy soil, and alluvial soil were 156.35, 145.82, 99.88, and 85.97 mg/L, respectively. For pH 3.5 of simulated acid rain, it was 130.49, 110.49, 80.57, and 62.73 mg/L, respectively. On leaching by simulated acid rain of pH 4.5, the maximum contents of REEs in the leachate were 53.46 and 29.82 mg/L, respectively, which were observed after leaching for 6 h in tailings and garden soil that became stable 12 h after leaching. The contents of leached REEs in paddy soil and alluvial soil were always in a lower and stable state. After eluviations with deionized water of pH 5.6, the contents of leached REEs in other soils were lower, except for the slight fluctuations in tailings. The maximum content in the leachate of REEs was in the water-soluble and exchangeable fraction. When bound to carbonate fractions, REEs were not detected in the leachate. REEs bound to iron-manganese (Fe–Mn) oxides fraction and to organic matter fraction in the leachate possibly came from the tested soil or from the REEs transformation during the migration process. The content of residual fraction REEs in the leachate was very low.

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