Coupling N‐doping and confined Co 3 O 4 on carbon nanotubes by polydopamine coating strategy for pleiotropic water purification

材料科学 催化作用 涂层 碳纳米管 降级(电信) 纳米技术 碳纤维 饮用水净化 化学工程 氧化还原 水处理 化学 复合材料 环境工程 有机化学 冶金 工程类 复合数 电信 计算机科学
作者
Wenlong Tu,Gang Wang,Yue Zhang,Hongyang Zhu,Rongrong Du,Hongyao Zhao,Sheng Tang,Zengjing Guo,Jun Yang,Fu Yang,Chengzhang Zhu
出处
期刊:Rare Metals [Springer Science+Business Media]
卷期号:43 (7): 3146-3160 被引量:42
标识
DOI:10.1007/s12598-024-02661-5
摘要

Abstract The development of effective and sustainable solutions for pleiotropic water purification becomes urgent and attractive. Heterogeneous Fenton‐like catalysts for activation of peroxymonosulfate (PMS) to purify organic wastewater show great promise. In this work, by tuning metal loading with an in‐situ polydopamine coating strategy, oxygen vacancy‐enriched Co 3 O 4 loading on N‐doped carbon nanotubes (CNTs) were constructed to enhance PMS activation efficiency for pollutants degradation. Impressively, the obtained modified CNTs afford a well‐developed N‐containing network structure, which is further endowed with abundant Co(II)/Co(III) redox cycles and significant metal–carbon interactions. In particular, the surface N doping in CNTs might induce the oriented enrichment of pollutants around the catalyst, which reduces the migration distance and correspondingly improves the utilization of reactive oxidative species. The electron transfer efficiency of the catalyst can be further improved by incorporating oxygen vacancy‐enriched Co 3 O 4 . The performance results show that the optimal NC/Co‐1 could mineralize 20 × 10 −6 of bisphenol A (BPA) by almost 98% in 8 min. A low reaction activation energy (26.05 kJ·mol −1 ) in BPA degradation was demonstrated by the NC/Co‐1. More importantly, NC/Co‐1 can inherit excellent degradation performance towards oxytetracycline, 2, 4‐dichlorophenol, and tetracycline, showing wide practical flexibility. In addition, by virtue of the photothermal conversion property, NC/Co‐1 achieves an additive function for interfacial solar water evaporation (1.84 kg·m −2 ·h −1 , 112.51%), showing impressive potential for clean water recovery under complicated environmental pollution conditions.
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