Degradation of diclofenac in water under LED irradiation using combined g-C3N4/NH2-MIL-125 photocatalysts

光降解 光催化 降级(电信) 微型多孔材料 激进的 石墨氮化碳 化学 核化学 化学工程 材料科学 光化学 催化作用 有机化学 电信 计算机科学 工程类
作者
Virginia Muelas-Ramos,Maria J. Sampaio,Cláudia G. Silva,Jorge Bedia,Juan J. Rodrı́guez,Joaquim L. Faria,Carolina Belver
出处
期刊:Journal of Hazardous Materials [Elsevier BV]
卷期号:416: 126199-126199 被引量:122
标识
DOI:10.1016/j.jhazmat.2021.126199
摘要

This study reports the photocatalytic degradation of diclofenac by hybrid materials prepared by combination of graphitic carbon nitride (g-C3N4) and titanium-metal organic framework (NH2-MIL-125), in different mass proportions (MOF:C3N4 of 25:75, 50:50 and 75:25). The hybrid materials were fully characterized, and their properties compared to those of the individual components, whose presence was confirmed by XRD. The porous structure was the result of the highly microporous character of the MOF and the non-porous one of g-C3N4. The band gap values were very close to that of MOF component. Photoluminescence measurements suggested an increase on the recombination rate associated to the presence of g-C3N4. Photodegradation tests of diclofenac (10 mg·L-1) were performed under UV LED irradiation at 384 nm. The hybrid materials showed higher photocatalytic activity than the individual components, suggesting the occurrence of some synergistic effect. The photocatalyst with a MOF:g-C3N4 ratio of 50:50 yielded the highest conversion rate, allowing complete disappearance of diclofenac in 2 h. Experiments with scavengers showed that superoxide radicals and holes played a major role in the photocatalytic process photodegradation, being that of hydroxyl radicals less significant. From the identification of by-products species, a degradation pathway was proposed for the degradation of diclofenac under the experimental operating conditions.
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