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Regenerable g-C(3)N(4)–chitosan beads with enhanced photocatalytic activity and stability

In this study, a series of regenerable graphitic carbon nitride–chitosan (g-C(3)N(4)–CS) beads were successfully synthesized via the blend crosslinking method. The prepared beads were characterized by scanning electron microscopy (SEM), thermogravimetric analysis (TGA), X-ray diffraction (XRD), Four...

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Detalles Bibliográficos
Autores principales: Zhao, Chaocheng, Yan, Qingyun, Wang, Shuaijun, Dong, Pei, Zhang, Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9083882/
https://www.ncbi.nlm.nih.gov/pubmed/35540016
http://dx.doi.org/10.1039/c8ra04293d
Descripción
Sumario:In this study, a series of regenerable graphitic carbon nitride–chitosan (g-C(3)N(4)–CS) beads were successfully synthesized via the blend crosslinking method. The prepared beads were characterized by scanning electron microscopy (SEM), thermogravimetric analysis (TGA), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), diffuse reflectance spectroscopy (DRS), photoluminescence (PL) spectroscopy, and X-ray photoelectron spectroscopy (XPS). The structural characterization results indicate that the g-C(3)N(4) granules were uniformly distributed on the surface of the chitosan matrix, and the structures of g-C(3)N(4) and CS are maintained. In addition, the prepared g-C(3)N(4)–CS beads exhibited efficient MB degradation and stability. The optimum photocatalytic activity of our synthesized g-C(3)N(4)–CS beads was higher than that of the bulk g-C(3)N(4) by a factor of 1.78 for MB. The improved photocatalytic activity was predominantly attributed to the synergistic effect between in situ adsorption and photocatalytic degradation. In addition, the reacted g-C(3)N(4)–CS beads can be regenerated by merely adding sodium hydroxide and hydrogen peroxide. Additionally, the regenerated g-C(3)N(4)–CS beads exhibit excellent stability after four runs, while the mass loss is less than 10%. This work might provide guidance for the design and fabrication of easily regenerated g-C(3)N(4)-based photocatalysts for environmental purification.