Abstract

A powdery lithium ion sieve (HMO) derived from biogenic birnessite was homogeneously integrated in sodium alginate (AL) beads. The composite beads were then characterized and their Li+ adsorption properties were investigated. Scanning electron microscopy–energy dispersive spectroscopy analysis showed that the HMO particles were homogeneously dispersed in the AL beads even after drying. The adsorption isotherm of Li+ adsorption to HMO encapsulated in AL beads (HMO–AL) was well fitted by the linear Langmuir model, and the beads showed a maximum adsorption capacity of 3.61mmol/g based on HMO, which is comparable with the value of the original powdery HMO. Kinetic studies revealed that adsorption of Li+ follows a pseudo-second-order model with rate constant k2=2.8–11.9×10−3g/(mmolmin) for the initial Li+ concentration range 2.56–4.23mM. Diffusion of Li+ from aqueous solution to the HMO particle through the Ca–AL network is the rate-limiting step for Li+ adsorption to HMO–AL beads. The HMO-AL beads enhanced the handling efficiency for Li+ adsorption and reused without significant reduction of Li+ adsorption efficacy.

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