1e:T537,An environmentally friendly leaching process for recycling valuable metals from spent lithium-ion batteries is developed. A sol–gel method is utilized to resynthesize LiNi1/3Co1/3Mn1/3O2 from the leachate. Lactic acid is chosen as a leaching and chelating agent. The leaching efficiency is investigated by determining the contents of metal elements such as Li, Ni, Co, and Mn in the leachate using inductively coupled plasma optical emission spectroscopy. The spent cathode materials for the pretreatment process and the regenerated and freshly synthesized materials are examined using X-ray diffraction and scanning electronic microscopy. The results show that the leaching efficiencies of Li, Ni, Co, and Mn reached 97.7, 98.2, 98.9, and 98.4%, respectively. The optimum conditions are lactic acid concentration of 1.5 mol L–1, solid/liquid ratio of 20 g L–1, leaching temperature of 70 °C, H2O2 content of 0.5 vol %, and reaction time of 20 min. The leaching kinetics of cathode scrap in lactic acid fit well to the Avrami equation. Electrochemical analysis indicate that the regenerated LiNi1/3Co1/3Mn1/3O2 cathode materials deliver a highly reversible discharge capacity, 138.2 mA h g–1, at 0.5 C after 100 cycles, with a capacity retention of 96%, comparable to those of freshly synthesized LiNi1/3Co1/3Mn1/3O2 cathodes.1f:T4a3,Membranes of sub-2-nanometer channels show high ion transport rates, but it remains a great challenge to design such membranes with desirable ion selectivities for ion separation applications. Here, covalent organic framework (COF) membranes with a channel size of ≈1.4 nm and abundant hydrogen bonding sites, exhibiting efficient ion sieving properties are demonstrated. The COF membranes have high monovalent cation permeation rates of 0.1-0.2 mol m^-2 h^-1 and extremely low multivalent cation permeabilities, leading to high monovalent over divalent ion selectivities for K⁺ /Mg²⁺ of ≈765, Na⁺ /Mg²⁺ of ≈680, and Li⁺ /Mg²⁺ of ≈217. Experimental measurements and theoretical simulations reveal that the hydrogen bonding interaction between hydrated cations and the COF channel wall governs the high selectivity, and divalent cations transport through the channel needs to overcome higher energy barriers than monovalent cations. These findings provide an effective strategy for developing sub-2-nanometer sized membranes with specific interaction sites for high-efficiency ionic separation.

	Year	Citations

References