g-C3N4增强Fe3+/ Fe2+循环激活PMS在太阳照射下降解药物

IF 2.3 4区 化学 Q3 CHEMISTRY, PHYSICAL
Liu Cheng, Zhexin Zhu, Gangqiang Wang, Shiting Du
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引用次数: 0

摘要

由于过氧单硫酸盐(Peroxymonosulfate, PMS)易得且能产生具有较强氧化能力的硫酸盐自由基,类fenton体系Fe2+/PMS在有机污染物降解中逐渐取代Fe2+/H2O2体系。然而,Fe3+/PMS体系几乎没有降解作用,Fe2+向Fe3+的转化是Fe3+/PMS体系的限速步骤。本文采用类石墨相氮化碳(g-C3N4),利用微量Fe3+激活PMS处理日光下的水污染,Fe3+/g-C3N4/PMS系统显示出快速降解各种难以降解的有机污染物的能力。Fe3+/g-C3N4/PMS体系能在30 min内完全降解卡马西平(CBZ)。研究表明,该系统有效地改善了Fenton工艺中金属离子与氧化剂进料比的严格限制,并且可以在很宽的pH范围内有效地降解CBZ。此外,为了避免大量“铁泥”的产生,实验中采用的Fe3+浓度为6.17 × 10−6 M。陷阱爆发实验、DMSO氧化实验和电子顺磁共振波谱实验表明,O2·−和1O2在CBZ的光催化降解反应中起主要作用,SO4·−和·OH共同促进CBZ的降解。图形抽象
本文章由计算机程序翻译,如有差异,请以英文原文为准。

g-C3N4 Enhanced Fe3+/ Fe2+ Cycling to Activate PMS for Pharmaceuticals Degradation Under Solar Irradiation

g-C3N4 Enhanced Fe3+/ Fe2+ Cycling to Activate PMS for Pharmaceuticals Degradation Under Solar Irradiation

Since Peroxymonosulfate (PMS) is readily available and can produce sulfate radicals with a stronger oxidation capacity, the Fenton-like system Fe2+/PMS has gradually replaced Fe2+/H2O2 system in organic pollutants degradation. However, the Fe3+/PMS system has almost no degradation effects, with the conversion of Fe2+ to Fe3+ being the rate-limiting step in the Fe3+/PMS system. In this paper, graphite-like phase carbon nitride (g-C3N4) was employed to activate PMS using trace amounts of Fe3+ for the treatment of water pollution under sunlight, and the Fe3+/g-C3N4/PMS system demonstrated the ability to rapidly degrade a wide range of difficult-to-degrade organic pollutants. The Fe3+/g-C3N4/PMS system was able to completely degrade carbamazepine (CBZ) within 30 min under sunlight. The fundings indicated that this system effectively improved the stringent limitations typically associated with Fenton process regarding the feed ratio of metal ions to oxidants, and could efficiently degrade CBZ across a broad pH range. In addition, the Fe3+ concentration of 6.17 × 10−6 M was used in the experiments to avoid the generation of large amounts of “iron sludge”. The trap burst experiments, DMSO oxidation experiments and electron paramagnetic resonance spectroscopy experiments indicated that O2· and 1O2 exerted the major effectiveness in the photocatalytic degradation reaction of CBZ, and SO4· and ·OH jointly promoted the CBZ degradation.

Graphical Abstract

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来源期刊
Catalysis Letters
Catalysis Letters 化学-物理化学
CiteScore
5.70
自引率
3.60%
发文量
327
审稿时长
1 months
期刊介绍: Catalysis Letters aim is the rapid publication of outstanding and high-impact original research articles in catalysis. The scope of the journal covers a broad range of topics in all fields of both applied and theoretical catalysis, including heterogeneous, homogeneous and biocatalysis. The high-quality original research articles published in Catalysis Letters are subject to rigorous peer review. Accepted papers are published online first and subsequently in print issues. All contributions must include a graphical abstract. Manuscripts should be written in English and the responsibility lies with the authors to ensure that they are grammatically and linguistically correct. Authors for whom English is not the working language are encouraged to consider using a professional language-editing service before submitting their manuscripts.
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