Lithium recovery from spent Li-ion batteries using coconut shell activated carbon. (September 2018) - Purnomo, Chandra Wahyu
Highlights: Activated carbon from coconut charcoal was activated chemically and physically. Chemical activation leads to larger ratio of micropore volume than physical one. Adsorbent porosity, liquid flowrate and grain size influences Li ions separation. Chemically activated sample provides better separation in column adsorption. In early period, Li-rich solution was obtained due to the fast travel time of Li. Abstract: Lithium is one of scarce natural resources in the world that need to be preserve. One of the way in preserving the resource is by recovery the rich source of the lithium such as in the spent batteries. It is necessary to develop a recovery method which is efficient and low-cost to be able to recover the lithium in an economic scale. In this study, low-cost activated carbon (AC) from coconut shell charcoal was prepared by chemical and physical activation methods and tested for Li removal from Co, Mn, and Ni ions in semi-continuous columns adsorption experiments. The maximum surface area is 365 m 2 /g with the total pore volume is 0.148 cm 3 /g that can be produced by physical activation at 800 °C. In the same activation temperature, activation using KOH has larger ratio of micropore volume than physical activation. Then, the adsorption capacity and selectivity of metal ions were investigated. A very low adsorption capacity of AC for Li ions in batch adsorption mode provides an advantage in column applications for separating Li from other metal ions. The AC sample with chemical activation provided better separation than the samples with physical activation in the column adsorption method. During a certain period of early adsorption (lag time), solution collected from the column outlet was found to be rich in Li due to the fast travel time of this light element, while the other heavier metal ions were mostly retained in the AC bed. The maximum lag time is 97.3 min with AC by KOH activation at 750 °C.