Battery Recycling: Mechanistic Modelling of LiCoO${}_2$ Leaching with Coupled Diffusion-Reaction Kinetics and Film Passivation

Abstract

We developed a new mechanistic model for lithium and cobalt recovery during acidic-reductive leaching from LiCoO${}_2$. The system considers HCl as an acid and H${}_2$O${}_2$ as a reducing agent. The model tracks conversion of LCO, the particle radius, the acid, H${}_2$O${}_2$, formation-dissolution dynamics of Co${}_3$O${}_4$ film, the film thickness, recovery of lithium and cobalt, and moles of O${}_2$. We introduced the film passivation effects for reduced recovery in the absence of H${}_2$O${}_2$. We validated the model against the experimental data of recovered Li and Co reported in literature at three acid concentrations (0.5 M, 1.5 M, and 2.5 M) and four H${}_2$O${}_2$ concentrations (0%, 0.2%, 0.4%, and 0.6% (v/v)). The model works reasonably well at 0.5 M and 1.5 M HCl for the 0% and 0.6% concentrations of H${}_2$O${}_2$. At 2.5 M HCl, the model over-predicts the data in the presence of H${}_2$O${}_2$, while it works well at 0% H${}_2$O${}_2$. We suggest pathways for further improvements in the model. The comprehensive mechanistic modelling framework for the leaching with a full list of the equations, the parameters, and the variables, reported for the first time, can be extended to other cathode chemistries and acid-reductive leaching systems.

arXiv comment45 pages