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The behaviour of selected rare-earth elements during the conversion of phosphogypsum to calcium sulphide and residue
Authors:Christophe  Nsaka Ntumba  McCrindle  Rob  Maree  Jannie  Ngole-Jeme  Veronica
Institution:1.Department of Environmental Sciences, School of Environmental Science, College of Agriculture and Environmental Sciences, Faculty of Sciences, Florida Campus, University of South Africa, Florida, Roodepoort, 1710, South Africa
;2.Department of Chemistry, Faculty of Science, Tshwane University of Technology, Private Bag X680, Pretoria, 0001, South Africa
;3.ROC Water Technologies, Die Wilgers, P O Box 70075, Pretoria, 0041, South Africa
;
Abstract:

Phosphogypsum (PG) is a large hazardous waste from fertiliser and phosphoric acid industries from which useful products including rare-earth elements (REEs) can be recovered depending on the treatment process. Its conversion to calcium sulphide (CaS) which was achieved at 95% followed by the formation of S, CaCO3 and residue is one of the plausible treatment processes leading to economic and environmental benefits. This study aimed at monitoring selected REEs behaviour during the conversion of (PG) to (CaS). The concentrations of REEs in the raw PG, the produced CaS and the obtained residue were determined after digestion (microwave and traditional acid leaching) using ICP-OES. The effect of CO2 and H2S used in the process of forming CaCO3 and S from PG on the concentrations of REEs was also investigated. Microwave digestion proved to be more effective than traditional acid leaching in the recovery of REEs. Microwave digestion using 3 mL HNO3?+?1 mL HCl was more effective than 1 mL HNO3?+?3 mL in REEs recovery. CaS contained the highest amount of Ce, Pr, Nd, Sm, Eu, Gd, Dy, Ho, Er, La and Y with values of 2646, 476, 2255, 320, 60.5, 376, 79.8, 1.24, 476, 1185 and 318 µg/g respectively. Based on these findings, the residue could be further processed to recover REEs despite less than 40% decrease in concentration for the majority of REEs observed due to the use of H2S and CO2. CO2 was found to be more suitable as fewer REEs were leached as compared to H2S. All things considered, the obtained residue could be a good secondary source of REEs as it is easier to leach, retained good amount of REEs and lesser impurities.

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