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CaO

Yue Pan1, Hanrui Su1, Yitong Zhu1

  • 1School of Environmental Science and Engineering, Shanghai Jiao Tong University, Shanghai, 200240, China.

Water Research
|September 15, 2018
PubMed
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Calcium peroxide (CaO2) significantly accelerates Fenton-like reactions at neutral pH by enhancing ferric ion (FeIII) reduction. This novel approach rapidly degrades phenol, overcoming limitations of traditional hydrogen peroxide (H2O2) systems.

Area of Science:

  • Environmental Chemistry
  • Advanced Oxidation Processes
  • Catalysis

Background:

  • Fenton-like reactions are crucial for pollutant degradation but limited by slow ferric ion (FeIII) reduction.
  • Achieving efficient degradation at neutral pH remains a significant challenge.

Purpose of the Study:

  • To dramatically accelerate Fenton-like reactions at neutral pH.
  • To investigate the use of calcium peroxide (CaO2) as an alternative hydrogen peroxide (H2O2) source.
  • To elucidate the mechanism behind the accelerated reaction.

Main Methods:

  • Utilized calcium peroxide (CaO2) as the H2O2 source and EDTA as a ferric ion chelator.
  • Performed phenol degradation experiments comparing CaO2 and H2O2 systems.
  • Employed Visual MINTEQ for speciation analysis and chloroform as a probe for superoxide radical (O2·-) detection.
Keywords:
Calcium peroxideFenton-like reactionHydrogen peroxideSuperoxide radicals

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  • Analyzed reaction kinetics and proposed a mechanistic pathway.
  • Main Results:

    • Phenol degradation was immediate and complete in 30 min with CaO2, compared to a 60 min lag phase in H2O2 systems.
    • Fe-EDTA- was identified as the active species.
    • Superoxide radical (O2·-) production was four orders of magnitude higher in the CaO2 system.
    • A mechanism involving two-electron transfer from CaO2 to FeIII-EDTA was proposed.

    Conclusions:

    • Calcium peroxide (CaO2) offers a superior alternative to H2O2 for Fenton-like reactions at neutral pH.
    • The enhanced reaction rate is attributed to efficient FeIII reduction facilitated by CaO2.
    • This study presents a promising strategy for organic pollutant removal and a novel source of superoxide radicals (O2·-).