4.7 Article

Ionothermal synthesis of Fe3O4 magnetic nanoparticles as efficient heterogeneous Fenton-like catalysts for degradation of organic pollutants with H2O2

Journal

JOURNAL OF HAZARDOUS MATERIALS
Volume 322, Issue -, Pages 152-162

Publisher

ELSEVIER
DOI: 10.1016/j.jhazmat.2016.02.073

Keywords

Advanced oxidation processes; Fe3O4; Ionothermal synthesis; Heterogeneous Fenton-like catalysts; H2O2

Funding

  1. National Natural Science Foundation of China [21571146, 51504170]
  2. Natural Science Foundation of Hubei Province [2014CFB795]

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Fe3O4 magnetic nanoparticles (MNPs) are attractive heterogeneous Fenton-like catalysts for oxidative degradation of organic pollutants with H2O2. Herein highly efficient and stable Fe3O4 MNPs (Fe3O4-op-DES, ca. 10 nm) were successfully prepared via a novel oxidative precipitation-combined ionothermal synthesis, which comprised oxidative precipitation of FeSO4.7H(2)O in choline chloride:2urea deep eutectic solvent. Among five different Fe3O4 particles tested, Fe3O4-op-DES MNPs exhibited the highest catalytic activity with the activation energy of 47.6 kJ mol(-1) for degradation of Rhodamine B (RhB) with H2O2 under the same conditions (Fe3O4 dosage of 0.50g L-1, H2O2 concentration of 40 mmol L-1, pH 6.4, 55 degrees C, 2 h). Fe3O4-op-DES MNPs were magnetically recoverable, and had good catalytic stability and recyclability without the need of regeneration (>98% degradation efficiency of RhB in 2h and pseudo first-order rate constant of 0.0376 min(-1) after having been continuously running for 12 h). The superior catalytic performance of Fe3O4-op-DES MNPs was attributed to the combination of multiple technologically important features, including the nanometer size, high Fe2+ content, large surface area, high density of surface active sites and stable crystal structure (no phase transformation, negligible iron leaching and particle aggregation after reaction). The wide applicability of Fe3O4-op-DES MNPs was also demonstrated by the degradation of four other organic pollutants. (C) 2016 Elsevier B.V. All rights reserved.

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