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Catalytic degradation of toxic organic dye using an aluminum‐doped Cu 0.4 Zn 0.6‐x Al x Fe 2 O 4 (x = 0.0, 0.2, 0.4, 0.6) spinel ferrite in a photo‐Fenton system

Catalytic activity of spinel ferrite in breaking down toxic dye materials are promising due to their uniqueness. In this study, aluminum‐doped copper zinc ferrite, Cu 0.4 Zn 0.6‐x Al x Fe 2 O 4 (x = 0.0, 0.2, 0.4, 0.6), a catalyst for toxic dye degradation is synthesized through chemical co‐precipit...

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Bibliographic Details
Published in:Environmental quality management 2023-06, Vol.32 (4), p.149-160
Main Authors: Akhter, Morsheda, Dutta, Sagar Kumar, Dhar, Palash Kumar, Ahmed, Jamil, Khan, Mohammed Nazrul Islam, Amin, Md. Khairul, Islam, Jahidul
Format: Article
Language:English
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Summary:Catalytic activity of spinel ferrite in breaking down toxic dye materials are promising due to their uniqueness. In this study, aluminum‐doped copper zinc ferrite, Cu 0.4 Zn 0.6‐x Al x Fe 2 O 4 (x = 0.0, 0.2, 0.4, 0.6), a catalyst for toxic dye degradation is synthesized through chemical co‐precipitation route. The formation of the spinel ferrite catalyst is initially confirmed by Fourier transform infrared spectra, which shows the frequency of metal‐oxygen bond vibration at 539 and 427 cm −1 attributed to the tetrahedral and octahedral sites respectively. Higher intensity sharp peak of X‐ray diffraction for (311) plane is the evidence for the phase purity and the formation of spinel ferrite. The crystallite size is found to decrease with the increase of Al 3+ ion. The surface structure of the obtained particles is investigated using a scanning electron microscope. Analyses of the material's magnetic characteristics using a vibrating sample magnetometer (VSM) revealed that it is, in fact, a soft magnet, as evidenced by the loop of its hysteresis, which is narrow. The catalytic degradation of methylene blue dye under the mechanism of the photo‐Fenton process is studied with the obtained spinel ferrites and the result is found to be as high as 96.5%. The process follows pseudo‐second order kinetics and the Langmuir isotherm.
ISSN:1088-1913
1520-6483
DOI:10.1002/tqem.21954