Abstract
A three-dimensionally macroporous–mesoporous lithium ion sieve (3DM-H4Ti5O12) was transformed from 3DM-Li4Ti5O12 through washing with HCl solution, which was synthesized by a combination of hydrothermal and low-temperature calcination (600 °C) treatment, using polystyrene microarray as hard-template, and titanium isopropoxide and lithium acetate as co-precursors. The influence of HCl concentration and temperature on the deintercalation rate of Li and Ti from Li4Ti5O12 was specifically explored to maximize the extraction ratio of Li/Ti. The acceleration of Li extraction and insertion in a porous structure was verified using nonporous Li4Ti5O12 as a control. 3DM-H4Ti5O12 showed superior Li+ adsorption performance (5.51 mmol/g) compared with its nonporous counterpart (1.12 mmol/g), which was ascribed to the reduced Li+ mass transfer resistance in the highly interconnected porous channel. The ion selectivity of the 3DM-H4Ti5O12 lithium ion sieve followed the order of Li+ > Na+ ~ Ca2+ > K+ > Mg2+. The adsorption performance could be maintained after six cycles. The high adsorption capacity, excellent selectivity, and good recyclability demonstrate the prosperous potential application of 3DM-H4Ti5O12.
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Acknowledgements
This work is supported by the National Natural Science Foundation of China (21673073, 21677048, U1407102 and 21377038), the National Basic Research Program of China (973 Program, 2013CB632403), the Science and Technology Commission of Shanghai Municipality (14230710500, 14ZR1410700 and 16JC1401400) and the Fundamental Research Funds for the Central Universities, PetroChina Innovation Foundation (2015D-5006-0402), the Fundamental Research Funds for the Central Universities (222201717003) and Collaborative Innovation Fund of Shanghai Institute of Technology (XTCX2015-9).
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Li, N., Gan, K., Lu, D. et al. Preparation of three-dimensional macroporous–mesoporous lithium ion sieve with high Li+ adsorption capacity. Res Chem Intermed 44, 1105–1117 (2018). https://doi.org/10.1007/s11164-017-3154-6
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DOI: https://doi.org/10.1007/s11164-017-3154-6