4.7 Article

Zn-MoS2 nanocatalysts anchored in porous membrane for accelerated catalytic conversion of water contaminants

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 398, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2020.125455

Keywords

Molybdenum disulfide; PVDF membrane; Hexavalent chromium; Formic acid; Interfacial effect

Funding

  1. National Natural Science Foundation of China [21876039]
  2. Anhui Provincial Natural Science Foundation [1708085 MB41]
  3. China Postdoctoral Science Foundation [2015 M570547, 2016 T90585]
  4. Australian Research Council [DP190103548]

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A series of Zn-MoS2 heterostructures were fabricated via a thermal-treatment method, and then anchored in polyvinylidene fluoride (PVDF) to yield novel catalytic membranes (Zn-MoS2@PVDF) by the phase inversion technique for enabling Cr-VI reduction. The SEM image showed that ZnS nanoparticles homogeneously coated on the MoS2 surface assembled in flower-like agglomerations. Zn-MoS2@PVDF exhibited unprecedented activity of Cr-VI reduction using formic acid (FA) as the reductant, with a high rate constant (k = 0.033 min(-1)) and low activation energy (Ea = 38.8 kJ mol(-1)). Cr-VI reduction rates effectively boosted with increasing FA dosages (0.234-1.170 M) and temperatures (15-55 degrees C), but declined with the increase of Cr-VI concentrations (5-25 mg/L), solution pHs (2.03-5.11) and inorganic salts. The excellent performance of Zn-MoS2@PVDF originated from the synergistic effect of the unique composition and electronic structure of the membranes. The strong electronic interactions of ZnS and MoS2 made an insignificant contribution to generate intermediate H-ads* and released molecular hydrogen. Rich porosity of PVDF membranes might not only afford a uniform dispersion of the Zn-MoS2 NPs, but also decrease mass transport resistance and provide an enlarged catalytic surface area. These outstanding characteristics indicate the potential applicability of Zn-MoS2@PVDF membranes for the remediation of heavy metal pollution.

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