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Magnetic Fe(3)O(4)@CoFe-LDH nanocomposite heterogeneously activated peroxymonosulfate for degradation of azo-dye AO7

In this study, a novel core@shell magnetic nanocomposite Fe(3)O(4)/CoFe-layered double hydroxide (Fe(3)O(4)@CoFe-LDH) was successfully synthesized by the co-precipitation method, and then employed as an efficient heterogeneous catalyst for activation of peroxymonosulfate (PMS) in removal of azo-dye...

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Detalles Bibliográficos
Autores principales: Sun, Dapeng, Li, Chuang, Lu, Shengsen, Yang, Qingfeng, He, Chiquan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033679/
https://www.ncbi.nlm.nih.gov/pubmed/35479896
http://dx.doi.org/10.1039/d1ra02973h
Descripción
Sumario:In this study, a novel core@shell magnetic nanocomposite Fe(3)O(4)/CoFe-layered double hydroxide (Fe(3)O(4)@CoFe-LDH) was successfully synthesized by the co-precipitation method, and then employed as an efficient heterogeneous catalyst for activation of peroxymonosulfate (PMS) in removal of azo-dye acid orange 7 (AO7). The as-obtained nanocomposite was characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM) and vibrating sample magnetometer (VSM). The results from these characterizations showed Fe(3)O(4)@CoFe-LDH to possess good ferromagnetism and a perfect crystalline structure with a typical core@shell morphology. The system of Fe(3)O(4)@CoFe-LDH11/PMS (cobalt : iron molar ratio of 1 : 1) achieved 95.1% removal rate of AO7 (40 mg L(−1)) within 15 min under the optimized conditions, which outperformed bare Fe(3)O(4) and raw CoFe-LDH11. Meanwhile, Fe(3)O(4)@CoFe-LDH11 displayed good adaptability in a wide pH range from 4 to 9 and relatively low PMS activation energy (39.9 kJ mol(−1)). The interference tests revealed HCO(3)(−) to possess the strongest restriction effect. Only 57.7% AO7 was removed when 10 mM HCO(3)(−) was introduced, which was ascribed to HCO(3)(−) not only serving as a radical scavenger, but also increasing the pH of the system. The radical quenching tests demonstrated SO(4)˙(−) as the dominant reactive species during the catalytic reaction. Based on X-ray photoelectron spectroscopy (XPS) analysis, the core structure of Fe(3)O(4) served as an electron donor for accelerating the cycle of Co(ii)/Co(iii) at the active site of the LDH outer shell. Also, Fe(3)O(4)@CoFe-LDH exhibited outstanding stability and recyclability, and maintained high degradation efficiency of AO7 even after five cycles. In sum, the proposed magnetic Fe(3)O(4)@CoFe-LDH nanocomposite has great potential for remediation of wastewater contaminated with synthetic dyes.