4.6 Article

Mn doping accelerates regeneration of Fe2+ in FeOOH and promotes efficient H2O2 activation for degradation of As(III)

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ELSEVIER
DOI: 10.1016/j.colsurfa.2022.130166

Keywords

Mn-FeOOH@CA; FeOOH; H2O2 activation; Fenton reaction; Arsenic oxidation

Funding

  1. National Natural Science Foundation of China [41977129, 21607176]
  2. Hunan Huxiang Young Talents Support Program, China [2020RC3044]
  3. Changsha Outstanding Innovative Youth Training Program [kq1802011]
  4. Natural Science Foundation of Hunan Province, China [2020JJ4136, 2022JJ90020]
  5. Research Foundation of Education Bureau of Hunan Province, China [16B274]
  6. Innovation Fund for Post-graduates of Central South University of Forestry and Technology [CX20192023]

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In this study, a carbonized aerogel decorated with Mn-FeOOH hybrid nanoparticles was prepared and used as a heterogeneous photo-Fenton catalyst. The Mn doping accelerated the regeneration of Fe2+ and promoted the decomposition of H2O2, leading to the production of hydroxyl radicals. The catalyst showed high efficiency and durability in degrading As(III) and has potential application in treating arsenic pollution.
In this study, a carbonized aerogel (CA) decorated with Mn-FeOOH hybrid nanoparticles was prepared and has been used as a better heterogeneous photo-Fenton catalyst. Mn doping accelerated the regeneration of Fe2+ and promoted the decomposition of H(2)O(2 )while producing many hydroxyl radicals (.OH), which solved the mass transfer problem in the traditional heterogeneous Fenton system. The amount of.OH in the Mn-FeOOH@CA/H2O2 system within 40 min was 2.4 times higher than that in the FeOOH@CA/H(2)O(2 )system, which further indicates that.OH was the main active species. High-porosity CA has been designed as an electron transport channel. During photocatalysis, electron transfer occurred between the Mn-FeOOH composite material and CA. The Fe2+ could be used as reaction sites to promote the activation of H(2)O(2 )on the surface of 1-Mn/FeOOH, and achieved 100 % As(III) degradation efficiency within 25 min. The catalyst maintained more than 80 % of its original oxidation capacity after five cycles of experiments, which indicates that it has good durability. This work is expected to provide rational design of heterometallic doped materials with oxygen vacancies to treat arsenic pollution.

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