Long-term leachability of Sb in smelting residue stabilized by reactive magnesia under accelerated exposure to strong acid rain.

This study investigated the long-term leachability of antimony (Sb) in a smelting residue (39519 mg/kg) solidified/stabilized by reactive magnesia (MgO). Different dosages of MgO (0% as control, 2%, 5%, and 10% on a dry basis) were compared, and the long-term performance was evaluated by an accelerated exposure test consist of 20 consecutive leaching steps with simulated strong acid rain (SAR, HNO3: H2SO4 = 1:2, pH = 3.20) as the extractant. Notably, the MgO treatments efficiently reduced the Sb leachability. Compared to the original slag (8.3 mg/L), the leaching concentrations based on a Chinese standard HJ/T299-2007 were reduced by 58%, 79%, 85%, and 86% at MgO dosages of 0%, 2%, 5%, and 10%, respectively. Because the studied slag was rich in oxides like SiO2, CaO, and MgO, the hydration reactions probably happened during the aging processes with oxic water. It was inferred that the formed hydration products have a self-solidification/stabilization function to suppress the Sb leaching from the solid phase. The mineralogical characterization results proved that the hydrated Mg(OH)2 played an essential role in the decrease of Sb leachability. Besides, the MgO addition promoted the hydration of this smelting slag and formed new hydrate gels that immobilize Sb in this slag. Our results confirmed that MgO-amended slags were resistant to continuous SAR corrosion. Compared to the control, the dosage of 5% MgO could effectively reduce the cumulatively released Sb by 57%, with only 0.46% of total Sb could be leached. The decomposition of Mg(OH)2 and hydrate gels determined the re-release of Sb in a long term. Our work has demonstrated that reactive MgO amendment could be potentially selected as an effective strategy for the treatment of Sb-containing smelting residues in field conditions.

Immobilization of Sb in a smelting residue by micro-sized zero-valent iron: Long-term performance under accelerated exposure to strong acid rain.

This study investigated the long-term leachability of antimony (Sb) in a smelting residue immobilized by three commercial micro-sized zero-valent iron (ZVI) products. Effect of oxic incubation time (14 days and 120 days) on the immobilization efficiency of Sb were compared, and the long-term leaching risk was evaluated by an accelerated exposure test, in which the slag was consecutively extracted by simulated strong acid rain (SSAR, HNO3: H2SO4 = 1:2, pH = 3.20). Notably, all ZVI treatments efficiently immobilized the Sb in this slag in a short term (14 days); the one-step SSAR-leached Sb was reduced by 89%-91% compared to the original slag (5.9 mg/L) and was far below the environmental standard (0.6 mg/L) established by the US EPA. The sequential SSAR leaching results reflected that the 14-d incubated slags after ZVI treatments had strong H+ resistance, and the immobilized Sb was not easily activated by continuous SSAR corrosion. The binding of Sb with amorphous phase Fe oxyhydroxides (e.g. ferrihydrite) derived from ZVI corrosion played a dominant role in the Sb immobilization efficiency. However, the longer aging process (120 days) easily resulted in the reduction of Sb immobilization by ZVI treatments. The changes in crystallinity of Fe oxyhydroxides (transformation from poorly-crystalline to crystalline ones) and the pH elevation to alkaline range might explain the weakening of the immobilization of Sb in ZVI-amended slags with 120 days of incubation. In total, the effectiveness of Sb immobilization in smelting residue greatly depended on the type of ZVI and the aging process. Our work has demonstrated that the ZVI treatment was potentially feasible to mitigate the Sb leaching risk from smelting slags; however, the ZVI type needs to be carefully selected and its long-term performance should be adequately verified before practical application.

Response of extracellular and intracellular alkaline phosphatase in Microcystis aeruginosa to organic phosphorus.

Cyanobacterial blooms caused by Microcystis have become a menace to public health and water quality in the global freshwater ecosystem. Alkaline phosphatases (APases) produced by microorganisms play an important role in the mineralization of dissolved organic phosphorus (DOP) into orthophosphate (Pi) to promote cyanobacterial blooms. However, the response of extracellular and intracellular alkaline phosphatase activity (APA) of Microcystis to different DOP sources is poorly understood. In this study, we compared the growth of M. aeruginosa on two DOP substrates (ß-glycerol-phosphate (ß-GP) and lecithin (LEC)) and monitored the changes of P fractions and the extra- and intracellular APA under different P sources and concentrations. M. aeruginosa can utilize both ß-GP and LEC to sustain its growth, and the bioavailability of LEC was greater than ß-GP. For the ß-GP treatment, there was no significant difference in the algal growth at different concentrations (P > 0.05), while the algal growth in the LEC treatment groups was significantly affected by concentrations (P < 0.05). The results showed that intracellular APA of M. aeruginosa could be detected in all DOP treatment groups and generally higher than extracellular APA. In addition, the intracellular APA per cell increased first and then decreased in all DOP treatment groups. Compared with the ß-GP treatment, M. aeruginosa in the LEC groups could secret more extracellular APA.