Enhanced Li+ adsorption by magnetically recyclable iron-doped lithium manganese oxide ion-sieve: Synthesis, characterization, adsorption kinetics and isotherm
The Li+ adsorption from aqueous solution by lithium-ion sieve has become one of the most promising methods due to the high efficiency and selectivity towards lithium ion (Li+). However, the industrial application of manganese oxide ion-sieve is limited due to its difficult separation and decrease of...
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Elsevier
2021-07-01
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author | Jian-ming Gao Zongyuan Du Qian Zhao Yanxia Guo Fangqin Cheng |
author_facet | Jian-ming Gao Zongyuan Du Qian Zhao Yanxia Guo Fangqin Cheng |
author_sort | Jian-ming Gao |
collection | DOAJ |
description | The Li+ adsorption from aqueous solution by lithium-ion sieve has become one of the most promising methods due to the high efficiency and selectivity towards lithium ion (Li+). However, the industrial application of manganese oxide ion-sieve is limited due to its difficult separation and decrease of adsorption capacity resulting from manganese dissolution loss. In this paper, the magnetically recyclable Fe-doped manganese oxide lithium ion-sieves with spinel-structure were proposed and prepared from LiMn2-xFexO4 synthesized by solid state reaction method. The effects of calcination temperature, calcination time and Fe doping amounts on the phase compositions, dissolution loss and adsorption performance of lithium ion-sieve precursors were systematically studied, and the influences of solution pH value, initial Li+ concentration and adsorption temperature on the adsorption performance were investigated. The adsorption mechanism was further discovered through adsorption kinetics and thermodynamics. The results show that the adsorption capacity of lithium ion-sieves could reach to 34.8 mg·g–1 when the calcination temperature, time and Fe doping content were controlled at 450 °C, 6 h, and 0.05, respectively. The Mn dissolution loss was reduced to 0.51%, much lower than the undoped lithium ion-sieve (2.48%), which is attributed to the inhibition of disproportionation reaction with the increasing proportion of Mn4+ in the skeleton. The adsorption process conformed to the pseudo-second-order kinetics equation and Langmuir isothermal adsorption model. Furthermore, the recycling performance of Fe-doped lithium ion-sieve showed that the adsorption capacity could remain 22.5 mg·g–1 (about 70%) after five cycles, which is greater than that of undoped lithium ion-sieve (about 50%), and the recovery of lithium ion-sieve can be realized by magnetic separation in an applying magnetic field. |
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last_indexed | 2024-12-21T17:26:36Z |
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spelling | doaj.art-0ee15ecf2d9a48ee8fdc04e30913cfdf2022-12-21T18:56:01ZengElsevierJournal of Materials Research and Technology2238-78542021-07-0113228240Enhanced Li+ adsorption by magnetically recyclable iron-doped lithium manganese oxide ion-sieve: Synthesis, characterization, adsorption kinetics and isothermJian-ming Gao0Zongyuan Du1Qian Zhao2Yanxia Guo3Fangqin Cheng4Institute of Resources and Environment Engineering, State Environmental Protection Key Laboratory of Efficient Utilization Technology of Coal Waste Resources, Shanxi Collaborative Innovation Center of High Value-added Utilization of Coal-related Wastes, Shanxi University, Taiyuan, 030006, PR ChinaInstitute of Resources and Environment Engineering, State Environmental Protection Key Laboratory of Efficient Utilization Technology of Coal Waste Resources, Shanxi Collaborative Innovation Center of High Value-added Utilization of Coal-related Wastes, Shanxi University, Taiyuan, 030006, PR ChinaInstitute of Resources and Environment Engineering, State Environmental Protection Key Laboratory of Efficient Utilization Technology of Coal Waste Resources, Shanxi Collaborative Innovation Center of High Value-added Utilization of Coal-related Wastes, Shanxi University, Taiyuan, 030006, PR ChinaCorresponding author.; Institute of Resources and Environment Engineering, State Environmental Protection Key Laboratory of Efficient Utilization Technology of Coal Waste Resources, Shanxi Collaborative Innovation Center of High Value-added Utilization of Coal-related Wastes, Shanxi University, Taiyuan, 030006, PR ChinaCorresponding author.; Institute of Resources and Environment Engineering, State Environmental Protection Key Laboratory of Efficient Utilization Technology of Coal Waste Resources, Shanxi Collaborative Innovation Center of High Value-added Utilization of Coal-related Wastes, Shanxi University, Taiyuan, 030006, PR ChinaThe Li+ adsorption from aqueous solution by lithium-ion sieve has become one of the most promising methods due to the high efficiency and selectivity towards lithium ion (Li+). However, the industrial application of manganese oxide ion-sieve is limited due to its difficult separation and decrease of adsorption capacity resulting from manganese dissolution loss. In this paper, the magnetically recyclable Fe-doped manganese oxide lithium ion-sieves with spinel-structure were proposed and prepared from LiMn2-xFexO4 synthesized by solid state reaction method. The effects of calcination temperature, calcination time and Fe doping amounts on the phase compositions, dissolution loss and adsorption performance of lithium ion-sieve precursors were systematically studied, and the influences of solution pH value, initial Li+ concentration and adsorption temperature on the adsorption performance were investigated. The adsorption mechanism was further discovered through adsorption kinetics and thermodynamics. The results show that the adsorption capacity of lithium ion-sieves could reach to 34.8 mg·g–1 when the calcination temperature, time and Fe doping content were controlled at 450 °C, 6 h, and 0.05, respectively. The Mn dissolution loss was reduced to 0.51%, much lower than the undoped lithium ion-sieve (2.48%), which is attributed to the inhibition of disproportionation reaction with the increasing proportion of Mn4+ in the skeleton. The adsorption process conformed to the pseudo-second-order kinetics equation and Langmuir isothermal adsorption model. Furthermore, the recycling performance of Fe-doped lithium ion-sieve showed that the adsorption capacity could remain 22.5 mg·g–1 (about 70%) after five cycles, which is greater than that of undoped lithium ion-sieve (about 50%), and the recovery of lithium ion-sieve can be realized by magnetic separation in an applying magnetic field.http://www.sciencedirect.com/science/article/pii/S2238785421004178Magnetically recyclableLithium-ion sieveFe-dopedLi adsorption kineticsStructure stability |
spellingShingle | Jian-ming Gao Zongyuan Du Qian Zhao Yanxia Guo Fangqin Cheng Enhanced Li+ adsorption by magnetically recyclable iron-doped lithium manganese oxide ion-sieve: Synthesis, characterization, adsorption kinetics and isotherm Journal of Materials Research and Technology Magnetically recyclable Lithium-ion sieve Fe-doped Li adsorption kinetics Structure stability |
title | Enhanced Li+ adsorption by magnetically recyclable iron-doped lithium manganese oxide ion-sieve: Synthesis, characterization, adsorption kinetics and isotherm |
title_full | Enhanced Li+ adsorption by magnetically recyclable iron-doped lithium manganese oxide ion-sieve: Synthesis, characterization, adsorption kinetics and isotherm |
title_fullStr | Enhanced Li+ adsorption by magnetically recyclable iron-doped lithium manganese oxide ion-sieve: Synthesis, characterization, adsorption kinetics and isotherm |
title_full_unstemmed | Enhanced Li+ adsorption by magnetically recyclable iron-doped lithium manganese oxide ion-sieve: Synthesis, characterization, adsorption kinetics and isotherm |
title_short | Enhanced Li+ adsorption by magnetically recyclable iron-doped lithium manganese oxide ion-sieve: Synthesis, characterization, adsorption kinetics and isotherm |
title_sort | enhanced li adsorption by magnetically recyclable iron doped lithium manganese oxide ion sieve synthesis characterization adsorption kinetics and isotherm |
topic | Magnetically recyclable Lithium-ion sieve Fe-doped Li adsorption kinetics Structure stability |
url | http://www.sciencedirect.com/science/article/pii/S2238785421004178 |
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