4.7 Article

Solar-driven on-site H2O2 generation and tandem photo-Fenton reaction on a triphase interface for rapid organic pollutant degradation

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 430, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2021.133168

Keywords

Triphase interface; Photocatalytic in-situ generation H2O2; Photo-Fenton; Environmental remediation; Water treatment

Funding

  1. National Natural Science Foundation of China [21876072, 22066021]
  2. Fundamental Research Funds for the Central Universities [lzujbky-2021-ct12]
  3. Special Fund Project for the Central Government
  4. Industrial support plan of Gansu Provincial Department of Education [2021cyzc-01]
  5. 111 Project [B20027]

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The article introduces a new method of in-situ generation and activation of hydrogen peroxide at triphase interface for efficient degradation of organic pollutants. By using Z-type heterojunction catalyst, the separation efficiency of photo-induced electrons and holes is improved, further enhancing the reaction efficiency.
Organic pollutants in wastewater have raised great concerns because of their considerable risk to human health and the ecosystem. Although Fenton reaction of advanced oxidation process represents a promising water treatment strategy. However, continuous consumption and low utilization efficiency of H2O2 limit its practical application. Herein, we propose photocatalytic in-situ production and activation H2O2 at triphase interface to reach excellent removal efficiency for contaminants. The triphase interface configuration allows oxygen rapid diffusion from the air to the surface of photocatalyst and avoids the problem of poor mass transfer of oxygen in solution. Meanwhile, using the Z-type heterojunction MIL-101(Fe)/g-C3N4 as model photocatalysts could largely promote the photo-induced electrons and holes separation efficiency to further improve reaction efficiency. As a result, the triphase photocatalytic system achieved an in-situ H2O2 production rate of 4370 mu mol h(-1) (greater than5 times higher than the diphase control) and a superior degradation efficiency for organic pollutants (model pollutant: methyl orange, concentration: 10 ppm, 99% removal rate in 130 min, while only 21% in diphase control) with a 17.5 times higher reaction rate constant. Therefore, the triphase photocatalytic system realized the highly efficient degradation of organic pollutants in wastewater by solar-driven, in-situ generation and activation of H2O2 with high catalytic activity and minimized oxygen transport limitation, thus providing a green and sustainable strategy for wastewater treatment and broadly environmental remediation.

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