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Preparation of a Gangue-Based X-type Zeolite Molecular Sieve as a Multiphase Fenton Catalyst and Its Catalytic Performance

[Image: see text] In this study, a series of X-type zeolite molecular sieve catalysts, modified with copper (Cu-X), were prepared by an alkali fusion–hydrothermal synthesis using coal gangue from Inner Mongolia. These catalysts were used in the degradation of the methylene blue dye by a Fenton-like...

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Detalles Bibliográficos
Autores principales: Zhang, MiaoSen, Wang, XiaoLi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8296578/
https://www.ncbi.nlm.nih.gov/pubmed/34308072
http://dx.doi.org/10.1021/acsomega.1c02469
Descripción
Sumario:[Image: see text] In this study, a series of X-type zeolite molecular sieve catalysts, modified with copper (Cu-X), were prepared by an alkali fusion–hydrothermal synthesis using coal gangue from Inner Mongolia. These catalysts were used in the degradation of the methylene blue dye by a Fenton-like reaction. Characterization results showed that Cu is considered to be present in the surface structure of the zeolite in the form of doped Cu ions and metal oxide. It is believed that Cu(2+) is the main active site involved in the Fenton reaction. The X-ray photoelectron spectroscopy (XPS) spectra indicated that Cu(2+) and Cu(+) coexist in the catalysts and participate together in the Fenton reaction. The degradation of methylene blue by the Cu-X catalysts was investigated to determine the optimal catalytic conditions in terms of six aspects: catalyst dosage, initial solution concentration, initial pH of the solution, H(2)O(2) dosage, copper loading, and reaction temperature. The experimental results showed that CX-1.0 had excellent activity and stability for the degradation and decolorization of the methylene blue dye, which could completely degrade the dye within 90 min, and the total organic carbon removal rate reached as high as 97.8%. Electron spin resonance (ESR) and radical capture experiments showed that (•)OH played a dominant role in the Fenton-like reaction. Combined with XPS, ESR, and catalytic tests, the redox cycle of Cu(+)/Cu(2+) was found to be accelerating the generation of reactive radicals in the Fenton system.