• 文献标题:   Enhanced photodegradation toward graphene-based MgFe2O4-TiO2: Investigation and optimization
  • 文献类型:   Article
  • 作  者:   VIET TQQ, PHONG HHT, THINH DB, GIANG NTH, DAT NM, HAI ND, PHONG MT, HIEU NH
  • 作者关键词:   pnitrophenol, hydrothermal, photodegradation, mgfe2o4, tio2, reduced graphene oxide
  • 出版物名称:   INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
  • ISSN:   0360-3199 EI 1879-3487
  • 通讯作者地址:  
  • 被引频次:   2
  • DOI:   10.1016/j.ijhydene.2022.07.119 EA SEP 2022
  • 出版年:   2022

▎ 摘  要

In this work, graphene-based MgFe2O4-TiO2 (MFO-TiO2@rCO) nanocomposite was synthesized and conducted an efficient photo-treatment with p-nitrophenol (PNP) as a well -known pollutant in water. The ternary material was characterized by modern analysis methods including Fourier transform infrared spectroscopy, X-ray diffraction, Raman spectroscopy, Transmission electron microscopy, Energy-dispersive X-ray spectroscopy, Selected area electron diffraction, and UV-vis spectroscopy. The simultaneous effects of the volume of H2O2, catalyst dosage, and pH on the photodegradation of p-nitrophenol were also examined by full factorial experimental design according to Box-Behnken designs. As a result, the characterization has confirmed the uniform bounding of MFO and TiO2 nanosizing from 4 to 6 nm on graphene with a high crystallinity degree. The photocatalysis of this material toward PNP can reach up to -99.44% in only 60 min reaction under UV control with 1.12 mL H2O2 added, 38.15 mg catalyst, and pH 9. Besides, in solar condition (directly under sun), the material also expressed a relatively impressive capability in degrade PNP from water. Furthermore, the ternary nanocomposite can be easily recycled and reused with an inconsiderable change in yield, represented by the elimination yield of recovered MFO-TiO2@rCO was significantly more than 90% after ten-run cycles. Indeed, the nanocomposite suggests an efficient pathway for treating organic contaminants in wastewater treatment. (C) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.