4.7 Article

Demand-oriented construction of Mo3S13-LDH: A versatile scavenger for highly selective and efficient removal of toxic Ag(I), Hg(II), As(III), and Cr(VI) from water

期刊

SCIENCE OF THE TOTAL ENVIRONMENT
卷 820, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.scitotenv.2022.153334

关键词

Ion-exchange; Mo3S13-LDH; Adsorbent; Selectivity; Toxic metal ions removal

资金

  1. National Natural Science Foundation of China [21675127]

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Inspired by classic ion-exchange reactions, a single phase material Mo3S13-LDH was successfully constructed with excellent binding affinity and high selectivity for Ag(I) and Hg(II) in a mixed solution, while also exhibiting high capture capacity for oxoanions such as As(III) and Cr(VI) and reducing their concentrations below safe drinking water limits. The rational design of Mo3S13-LDH, with multiple sulfur ligands and large-sized Mo3S132- groups, plays a key role in its performance for water remediation applications.
Inspired by the classic ion-exchange reaction, a single phase material of Mg0.66Al0.34(OH)(2)(Mo3S13)(0.03)(NO3)(0.14) (CO3)(0.07).H2O (Mo3S13-LDH) was masterly constructed by intercalating Mo3S132- into the MgAl-LDH gallery. Prepared Mo3S13-LDH displays excellent binding affinity and high selectivity for Ag(I) and Hg(II) in a mixed solution, in which an apparent selectivity order of Hg(II) > Ag(I) >> Pb(II), Cu(II), Ni(II), Co(II), Cd(II), and Mn(II) is observed. Enormous capture capacities (qmAg = 446.4 mg/g, qmHg= 354.6 mg/g) and fast equilibration time (within 60 min) place Mo3S13- LDH in the upper ranks of materials for such removal. For oxoanions, As(III) (HAsO32-) and Cr(VI) (CrO42-) can be specifically trapped by Mo3S13-LDH with comparable loading ability (q(m)(As) = 61.8 mg/g, q(m)(Cr) = 90.6 mg/g) in the coexistence of multiple interfering anions. Notably, high Hg(II) and Cr(VI) concentrations are finally reduced below the safe limit of drinking water. The excellent capture capacity of Mo3S13-LDH benefits from the rational design by following two aspects: (i) the multiple sulfur ligands in Mo3S132- groups give place to various capture modes and different affinity orders for target ions, and (ii) large-sized Mo3S132- groups widen the interlayer spacing of LDH, thereby accelerating the mass transfer process. Furthermore, the satisfactory structural stability of Mo3S13-LDH is also reflected through the unchanged hexagonal prismatic shape after adsorption. All of these highlight the great potential of Mo3S13-LDH for the application in water remediation.

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