Loading…

Fe3O4-NPs/orange peel composite as magnetic heterogeneous Fenton-like catalyst towards high-efficiency degradation of methyl orange

Magnetite nanoparticles (Fe3O4-NPs)/orange peel (MOP) composite was prepared via one-step in-situ co-precipitation method as magnetic heterogeneous Fenton-like catalyst. The properties of MOP were characterized by scanning electron microscopy, transmission electron microscopes, Brunauer–Emmett–Telle...

Full description

Saved in:
Bibliographic Details
Published in:Water science and technology 2021-07, Vol.84 (1), p.159-171
Main Authors: Zhao, Qiang, Zhang, Congcong, Tong, Xiaoqiang, Zou, Yunling, Li, Yan, Wei, Fang
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Magnetite nanoparticles (Fe3O4-NPs)/orange peel (MOP) composite was prepared via one-step in-situ co-precipitation method as magnetic heterogeneous Fenton-like catalyst. The properties of MOP were characterized by scanning electron microscopy, transmission electron microscopes, Brunauer–Emmett–Teller, X-ray diffraction, Fourier-transform infrared, thermogravimetric analysis and X-ray photoelectron spectroscopy technologies. Its Fenton-like catalytic responses towards removal of methyl orange (MO) were investigated, in which the effects of initial dye concentration, pH, temperature and hydrogen peroxide dosage were studied. The MO degradation ratio up to 98.0% was obtained within 20 min in optimized conditions. The catalyst showed excellent catalytic stability exhibiting nearly 90% degradation ratio in the 10th cycle within 20 min, whereas pure Fe3O4-NPs showed only 62.5% in this stage. Due to the stabilization of complexing orange peel hydroxyl to iron oxide in the composite and its magnetic separation property, MOP composite exhibits excellent Fenton-like catalytic performance, which offers great prospects for low-cost and high-efficiency organic dye wastewater treatment.
ISSN:0273-1223
1996-9732
DOI:10.2166/wst.2021.221