过硫酸盐
电子转移
碳纤维
兴奋剂
化学
氮气
电子
无机化学
材料科学
化学工程
光化学
催化作用
有机化学
物理
光电子学
量子力学
复合数
工程类
复合材料
作者
Ziyi Jiang,Zhonglian Shi,Chao Li,Huiqing Wang,Yingping Huang,Liqun Ye
出处
期刊:Langmuir
[American Chemical Society]
日期:2024-09-19
卷期号:40 (39): 20584-20595
被引量:14
标识
DOI:10.1021/acs.langmuir.4c02321
摘要
The incorporation of nitrogen into carbon materials is a strategy that effectively boosts their catalytic potency. Herein, a nitrogen-enriched carbon substance, designated as CN0.6, was synthesized from melamine, serving as a precursor. This substance has been established to act as an efficient catalyst devoid of metals for the activation of peroxymonosulfate (PMS). At a temperature of 25 °C, a concentration of 0.05 g/L CN0.6 along with 1 mM PMS suffices to achieve the complete degradation of concentrated tetracycline hydrochloride (TC) in a short period of 4 min. This enhanced catalytic performance is attributed to the optimal level of nitrogen doping, which elevates the pyrrolic nitrogen content and introduces additional defects characterized by an ID/IG ratio of 1.02. These factors collectively augment the adsorptive capacity for PMS and create a greater number of active sites to facilitate its activation. The dominance of a nonradical electron transfer mechanism in the CN0.6/PMS system has been confirmed through a series of analyses, including radical identification, quenching tests, and electrochemical assessments. Employing high-resolution liquid chromatography coupled with tandem mass spectrometry (LC-MS), the investigation identified three potential degradation routes for TC. Furthermore, the intermediates produced are determined to possess reduced toxicity in comparison to TC. The findings of this study offer a approach to the synthesis of highly efficient nitrogen-doped, metal-free catalysts, presenting a promising strategy for the degradation of environmental pollutants.
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