4.6 Article

Extraction of lithium from salt lake brines by granulated adsorbents

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ELSEVIER
DOI: 10.1016/j.colsurfa.2021.127256

关键词

Adsorption; Porous lithium adsorbents; Hydrothermal synthesis; Granulation; Salt lake brines

资金

  1. Natural Science Foun-dation of Qinghai Province [2020-ZJ-901, 2019-HZ-808]
  2. National Natural Science Foundation of China [U20A20141]

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Hierarchical meso- and macro-porosity enhance the adsorption capacity of lithium adsorbents, while granulation of powder lithium adsorbents improves their applicability. Granulated lithium adsorbents consisting of Li-Al-LDHs and NH4Al3(SO4)(2)(OH)(6) via crosslinking sodium alginate were successfully prepared and evaluated for adsorption-desorption performance. The granulated lithium adsorbents showed potential for industrial application, with a lithium adsorption capacity of 9.66 mg/g and fitting well with the Langmuir model for adsorption isotherm.
Hierarchical meso- and macro-porosity increases the adsorption capacity of lithium adsorbents and the granulation of powder lithium adsorbents raises the applicability of lithium adsorbents. Granulated lithium adsorbents consisting of porous mixtures of Li-Al-LDHs (layered double hydroxide) and NH4Al3(SO4)(2)(OH)(6) by crosslinking sodium alginate were successfully prepared, and adsorption-desorption performance of granulated adsorbents was evaluated. The adsorption capacity of granulated lithium adsorbents reached 9.66 mg/g (at the loading capacity of 83.3% by mass, 25 degrees C, and pH=6). The granulated lithium adsorbents were prepared in three steps. First, porous precursors of NH4Al3(SO4)(2)(OH)(6) and gamma-AlOOH were synthesized hydrothermally using Al-2(SO4)(3)center dot 18H(2)O and Urea. The porous powder precursors were then lithiated in aqueous LiOH solution to give mixed porous powders of NH4Al3(SO4)(2)(OH)(6) and Li-Al-LDHs of Li2Al4(OH)(12)SO4 center dot xH(2)O. Lithiated powder precursors were finally granulated by ionic crosslinking sodium alginate in CaCl2 aqueous solutions and deintercalated using water. The precursors and lithiated precursors were characterized by IR spectroscopy, powder XRD, XPS spectroscopy, SEM, TEM, thermal analyses, particle size analysis, and BET surface area. The adsorption isotherm, adsorption kinetics, the effects of pH, temperature, initial lithium concentration, and the anions and cations interference on lithium adsorption-desorption performance of granulated lithium adsorbents were studied. The adsorption isotherm and adsorption kinetics were best fitted with the Langmuir model and pseudosecond-order rate equation, respectively. Lithium adsorption was an endothermic process. The granulated lithium adsorbents were applied to real East Taigener salt lake brine. The lithium adsorption capacity dropped slightly to 9.16 mg/g; the adsorption equilibrium reached within 180 min; the dissolution rate was 0.54% after 10 cycles of adsorption and desorption. The granulated lithium adsorbents prepared show the potential in industrial application.

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