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Overcoming clay structure challenges in lithium recovery from boron waste using high‐temperature pressure acid leaching
Boron mines contain significant amounts of lithium along with boron. After boron is extracted, lithium remains in the waste, which has a carbonate‐hosted clay‐type structure, along with other impurities. The scarcity of lithium resources and the increasing need for lithium worldwide make such resour...
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Published in: | Canadian journal of chemical engineering 2024-11 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | Boron mines contain significant amounts of lithium along with boron. After boron is extracted, lithium remains in the waste, which has a carbonate‐hosted clay‐type structure, along with other impurities. The scarcity of lithium resources and the increasing need for lithium worldwide make such resources economically important. Although the best hydrometallurgical method for the recovery of lithium trapped within the clay‐structured mineral resources is roasting with chemicals to disrupt the clay structure and acid leaching, the process is quite difficult and costly due to the high energy and chemical addition requirements. To overcome this challenge, this study proposed a high‐temperature–pressure sulphuric acid leaching process to recover lithium from the boron waste. Under the optimized conditions (liquid/solid ratio: 10, acid concentration: 1 M, temperature: 150°C, and contact time: 120 min), 100% of lithium was leached. The leaching mechanism was determined through mineral characterization (X‐ray diffractometry [XRD], X‐ray fluorescence spectrophotometer [XRF], scanning electron microscopy–energy‐dispersive X‐ray spectroscopy [SEM–EDX], Mastersizer), and a shrinking core heterogeneous kinetics model. It was found that high‐temperature–pressure sulphuric acid leaching disrupted clay structure and promoted the leaching of lithium, the leaching kinetics fit the shrinking core heterogeneous kinetics model, and was controlled by a dual mechanism with ash diffusion and chemical reactions on the particle surface. The reaction rate constants increased with increasing temperature, and the activation energy was found to be 32.17 kJ/mol. |
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ISSN: | 0008-4034 1939-019X |
DOI: | 10.1002/cjce.25537 |