酞菁
化学
催化作用
配体(生物化学)
反应性(心理学)
甲基橙
光化学
药物化学
有机化学
光催化
受体
医学
生物化学
替代医学
病理
作者
Yan Ding,Kangping Cui,Xueyan Liu,Chen‐Xuan Li,Zhi Guo,Minshu Cui,Yihan Chen
标识
DOI:10.1016/j.apcata.2022.118679
摘要
Herein, a new axial g-C3N4 coordinated iron(III) phthalocyanine (FeP/CN) was fabricated for peroxymonosulfate (PMS) activation. Around 100% degradation of acetaminophen (AP), 2,4-dichlorophenol (2,4-DP), sulfadiazine (SDZ), and methyl orange (MO) (30 mg L-1) were achieved within 20 min by adding 0.02 g L-1 FeP/CN5 (3.62 wt% Fe) and 0.2 mM PMS. High-valent iron-oxo species (FeIV=O) was demonstrated as the main reactive species, which mediated a two-electron transfer process with pollutants. Characterizations and computational analysis revealed that the axial g-C3N4 ligand provided Fe(III) coordination environments to generate FeIV=O species directly through PMS activation, and increased the reactivity of the FeIV=O species in pollutants oxidation due to the narrowed HOMO-LUMO gap. Besides, small displacement of Fe atom (0.23 Å) from the macrocycles plane due to the axial g-C3N4 ligand decreased the iron demetalization rate from 3.54% to 0.28% in the catalyst/PMS system. This work offered an excellent strategy to design high-efficiency catalysts for FeIV=O generation.
科研通智能强力驱动
Strongly Powered by AbleSci AI