4.7 Article

Oxidative degradation of acid red 73 in aqueous solution over a three-dimensional OMS-2 nanomaterial

Journal

SEPARATION AND PURIFICATION TECHNOLOGY
Volume 263, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.seppur.2021.118397

Keywords

Oxidative degradation; Heterogeneous oxidation; OMS-2; Three-dimensional material

Funding

  1. National Natural Science Foundation of China [21403256, 21573261, 21805166]
  2. Youth Innovation Promotion Association CAS [2018456]
  3. LICP Cooperation Foundation for Young Scholars [HZJJ20-10]
  4. outstanding young and middle-aged science and technology innovation teams, Ministry of Education, Hubei province, China [T2020004]
  5. 111 Project of China [D20015]
  6. Engineering Research Center of Eco-environment in Three Gorges Reservoir Region, Ministry of Education, China Three Gorges University [KF2019-05]

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Ce and Bi co-doped OMS-2 showed enhanced oxidation reactivity and recyclability for the degradation of acid red 73 due to its unique morphology and rich surface oxygen vacancies. Moreover, co-doping significantly lowered the apparent activation energy, improving the degradation process efficiency.
Manganese oxide octahedral molecular sieve (OMS-2) and doped derivatives were synthesized via a one-pot reflux method and used in heterogeneous oxidative degradation of acid red 73 in aqueous solution. Doping metals and dopant loading influenced morphology and oxidation ability of the OMS-2-based materials significantly. Ce and Bi co-doped OMS-2 (Ce-Bi-OMS-2) demonstrated enhanced oxidation reactivity and recyclability for the degradation of acid red 73 because of the unique three-dimensional morphology, the enhanced surface area and the rich surface oxygen vacancies. About 96% of acid red 73 at a concentration of 200 mg/L was degraded under neutral conditions over Ce-Bi-OMS-2 doped by 8 wt% metals. COD and TOC removal efficiencies were 33% and 25% respectively, and the toxicity of the wastewater to Escherichia coli was reduced by Ce-Bi-OMS2 mediated degradation. The degradation pathway was carefully investigated and kinetic study indicated that the co-doping substantially lowered the apparent activation energy from 31.22 kJ/mol (original OMS-2) to 18.48 kJ/ mol.

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