Kinetic modeling of the leaching of LiCoO2 with phosphoric acid

In this article, we analyze the leaching kinetics with phosphoric acid of LiCoO2 samples from spent Li-ion batteries and commercial LiCoO2. The purpose was to study the mechanism by which the extraction reaction of cobalt and lithium is produced from the solid samples. The experimental results showe...

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Detalles Bibliográficos
Autores: Pinna, Eliana Guadalupe, Drajlin Gordón, Diego Sebastián, Toro, Norman, Rodriguez, Mario Humberto
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2020
País:Argentina
Institución:Consejo Nacional de Investigaciones Científicas y Técnicas
Repositorio:CONICET Digital (CONICET)
Idioma:inglés
OAI Identifier:oai:ri.conicet.gov.ar:11336/140440
Acceso en línea:http://hdl.handle.net/11336/140440
Access Level:acceso abierto
Palabra clave:LiCoO2
KINETIC MODEL
LIBs
SURFACE CHEMICAL REACTION
https://purl.org/becyt/ford/2.4
https://purl.org/becyt/ford/2
Descripción
Sumario:In this article, we analyze the leaching kinetics with phosphoric acid of LiCoO2 samples from spent Li-ion batteries and commercial LiCoO2. The purpose was to study the mechanism by which the extraction reaction of cobalt and lithium is produced from the solid samples. The experimental results showed that raising the temperature and the reaction time contributed to improving both the extraction of Li and Co from the structure. The leaching rate of the metals from both samples in the phosphoric acid solution could be expressed as: ln (1 − X) = −b1 [ln (1 + b2t) − 1+b2bt2t]. The morphology of the solid revealed that the dissolution reaction of the samples develops from preferential growth of active sites, points susceptible to chemical interaction, occurring in one direction, giving rise to the start and progress of the reaction. The generation of these sites in the LCO-H3PO4 reaction system is of the "sequential type". The apparent activation energy values for the leaching of Co and Li would indicate that the surface chemical reaction is the rate-controlling step during this dissolution process.