Metal-free activation of peroxymonosulfate by boron and nitrogen co-doped graphene nanotubes for catalytic oxidation of 4-hydroxybenzoic acid

Hong Wu , Abdul Hannan Asif , Lei Shi , Rajan Arjan Kalyan Hirani , Nasir Rafique , Hongqi Sun
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引用次数: 8

Abstract

Recently metal-free catalysts become very promising in environmental catalysis own to the nature of being free of metals for avoiding metal leaching-related secondary contamination. Herein, a series of boron and nitrogen co-doped graphene nanotubes were first synthesised by thermal treatment of urea, boric acid, and polyethene glycol (PEG, 2000). The materials fabricated under varied thermal conditions, e.g., different pyrolysis temperature and retention time, were characterised through advanced physiochemical techniques. The as-prepared materials showed outstanding catalytic activity for degradation of 4-hydroxybenzoic acid (HBA) via peroxymonosulfate (PMS) activation, whereas the catalyst pyrolysed at 1100 ​°C for 6 ​h (BNG-1100-6h) was found to be the best candidate for environmental remediation, thanks to its engineered surface, exposed active sites, and well-tuned functional groups. Based on the optimal carbocatalyst, reaction conditions such as catalyst loading, PMS dosage, solution pH, and reaction temperature were thoroughly investigated to make it a cost-effective catalytic system. A thermal regenerative path was adopted to enhance the catalyst stability and reusability. Quenching tests and electron paramagnetic resonance (EPR) spectroscopic analysis further revealed the dominant role of singlet oxygen (1O2), a non-radical reactive species, in the degradation of HBA. The current research work will not only provide a facile strategy for development of a carbocatalytic system but also open a new perspective for degradation of emerging contaminants such as HBA via a non-radical route.

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硼氮共掺杂石墨烯纳米管催化氧化4-羟基苯甲酸的无金属活化研究
近年来,由于不含金属以避免金属浸出相关的二次污染,无金属催化剂在环境催化中变得非常有前途。在此,通过对尿素、硼酸和聚乙二醇(PEG,2000)进行热处理,首次合成了一系列硼和氮共掺杂的石墨烯纳米管。通过先进的物理化学技术对在不同热条件下(如不同的热解温度和停留时间)制备的材料进行了表征。所制备的材料通过过氧一硫酸盐(PMS)活化对4-羟基苯甲酸(HBA)的降解表现出突出的催化活性,而催化剂在1100​°C持续6​h(BNG-1100-6h)被发现是环境修复的最佳候选者,这要归功于其工程化的表面、暴露的活性位点和良好调节的官能团。在最佳碳催化剂的基础上,对催化剂负载量、PMS用量、溶液pH和反应温度等反应条件进行了深入研究,使其成为一种经济高效的催化体系。采用热再生路径来提高催化剂的稳定性和可重复使用性。猝灭试验和电子顺磁共振(EPR)光谱分析进一步揭示了单线态氧(1O2),一种非自由基反应性物质,在HBA降解中的主导作用。目前的研究工作不仅为碳催化系统的开发提供了一种简单的策略,而且为通过非自由基途径降解HBA等新兴污染物开辟了一个新的视角。
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