Removal of Fe and Mn from Co leach solutions by adsorption on activated carbon based on post-consumer polyethylene terephthalate (PET) - Mechanism insights through linear and nonlinear isotherm and kinetic models

Abstract

ABSTRACT The removal of Fe2+ and Mn2+ from cobalt sulfate-saturated solutions is frequently problematic for Cu-Co hydrometallurgical process performance. Among the applied and developed methods for the removal of these metals, adsorption has drawn less attention. This study investigates on the removal of Fe2+ and Mn2+ in industrial cobalt solutions known as raffinates by adsorption on activated carbon prepared from post-consumer polyethylene terephthalate (PET). The adsorption operating conditions were studied in synthetic solutions and industrial solutions. The Langmuir, Freundlich, and Temkin isotherms were then used to fit the adsorption data, while the pseudo-first-order (PFO), pseudo-second-order (PSO), and Elovich models were used to describe the kinetics. Linear and nonlinear kinetic and isotherm models were studied and compared. Furthermore, intraparticle diffusion (IPD) models were used to study the transfer mass mechanism. The results show that Fe2+ and Mn2+ are removed from Co solutions with the efficiencies of 62.14 and 68.43, respectively. The Langmuir model fits the Fe2+ and Mn2+ adsorption data better, indicating that chemisorption is preferred over physisorption, whereas the Freundlich model fits the Co2+ adsorption data better, indicating that physisorption is preferred over chemisorption. The PFO model describes well the kinetic behavior of Fe2+ and Mn2+, whereas the Elovich model describes better the kinetic behavior of Co2+. According to the IPD model, the step that limits the adsorption of Fe2+, Mn2+, and Co2+ is essentially diffusion through the activated carbon pores. The reported experimental results will highlight the use of activated carbon in the removal of Fe2+ and Mn2+ in Cu and Co hydrometallurgy.