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Study on valuable metal incorporation in the Fe–Al precipitate during neutralization of LIB leach solution

The role of aluminum concentration and pH in the purification of waste Li-ion battery leach solution was investigated using NaOH and LiOH as neutralization agents ([H(2)SO(4)] = 0.313 M, t = 6 h). Solution was prepared from synthetic chemicals to mimic real battery leach solution. Results demonstrat...

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Autores principales: Chernyaev, Alexander, Wilson, Benjamin P., Lundström, Mari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8640047/
https://www.ncbi.nlm.nih.gov/pubmed/34857788
http://dx.doi.org/10.1038/s41598-021-02019-2
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author Chernyaev, Alexander
Wilson, Benjamin P.
Lundström, Mari
author_facet Chernyaev, Alexander
Wilson, Benjamin P.
Lundström, Mari
author_sort Chernyaev, Alexander
collection PubMed
description The role of aluminum concentration and pH in the purification of waste Li-ion battery leach solution was investigated using NaOH and LiOH as neutralization agents ([H(2)SO(4)] = 0.313 M, t = 6 h). Solution was prepared from synthetic chemicals to mimic real battery leach solution. Results demonstrate that pH (3.5–5.5) has a significant effect on the precipitation of metals (Fe, Al, Ni, Cu, Co, Mn, and Li), whereas higher temperature (T = 30 and 60 °C) decreases the precipitation pH of metals. Iron and aluminum were both found to precipitate at ca. pH 4 and the presence of aluminum in PLS clearly decreased the separation efficiency of Fe vs. active material metals (Ni, Co, Li). In the absence of dissolved aluminum, Fe precipitated already at pH 3.5 and did not result in the co-precipitation of other metals. Additionally, the Al-free slurry had a superior filtration performance. However, aluminum concentrations of 2 and 4 g/L were found to cause loss of Ni (2–10%), Co (1–2%) and Li (2–10%) to the Fe-Al hydroxide cake at pH 4. The use of LiOH (vs. NaOH) resulted in 50% lower co-precipitation of Ni, Co and Li. Overall, these results demonstrate that hydroxide precipitation can be an effective method to remove iron from battery waste leach solutions at aluminum concentrations of < 2 g/L only. Although the highest level of lithium loss in the cake was found at pH 4, the loss was shown to decrease with increasing pH.
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spelling pubmed-86400472021-12-06 Study on valuable metal incorporation in the Fe–Al precipitate during neutralization of LIB leach solution Chernyaev, Alexander Wilson, Benjamin P. Lundström, Mari Sci Rep Article The role of aluminum concentration and pH in the purification of waste Li-ion battery leach solution was investigated using NaOH and LiOH as neutralization agents ([H(2)SO(4)] = 0.313 M, t = 6 h). Solution was prepared from synthetic chemicals to mimic real battery leach solution. Results demonstrate that pH (3.5–5.5) has a significant effect on the precipitation of metals (Fe, Al, Ni, Cu, Co, Mn, and Li), whereas higher temperature (T = 30 and 60 °C) decreases the precipitation pH of metals. Iron and aluminum were both found to precipitate at ca. pH 4 and the presence of aluminum in PLS clearly decreased the separation efficiency of Fe vs. active material metals (Ni, Co, Li). In the absence of dissolved aluminum, Fe precipitated already at pH 3.5 and did not result in the co-precipitation of other metals. Additionally, the Al-free slurry had a superior filtration performance. However, aluminum concentrations of 2 and 4 g/L were found to cause loss of Ni (2–10%), Co (1–2%) and Li (2–10%) to the Fe-Al hydroxide cake at pH 4. The use of LiOH (vs. NaOH) resulted in 50% lower co-precipitation of Ni, Co and Li. Overall, these results demonstrate that hydroxide precipitation can be an effective method to remove iron from battery waste leach solutions at aluminum concentrations of < 2 g/L only. Although the highest level of lithium loss in the cake was found at pH 4, the loss was shown to decrease with increasing pH. Nature Publishing Group UK 2021-12-02 /pmc/articles/PMC8640047/ /pubmed/34857788 http://dx.doi.org/10.1038/s41598-021-02019-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Chernyaev, Alexander
Wilson, Benjamin P.
Lundström, Mari
Study on valuable metal incorporation in the Fe–Al precipitate during neutralization of LIB leach solution
title Study on valuable metal incorporation in the Fe–Al precipitate during neutralization of LIB leach solution
title_full Study on valuable metal incorporation in the Fe–Al precipitate during neutralization of LIB leach solution
title_fullStr Study on valuable metal incorporation in the Fe–Al precipitate during neutralization of LIB leach solution
title_full_unstemmed Study on valuable metal incorporation in the Fe–Al precipitate during neutralization of LIB leach solution
title_short Study on valuable metal incorporation in the Fe–Al precipitate during neutralization of LIB leach solution
title_sort study on valuable metal incorporation in the fe–al precipitate during neutralization of lib leach solution
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8640047/
https://www.ncbi.nlm.nih.gov/pubmed/34857788
http://dx.doi.org/10.1038/s41598-021-02019-2
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