通过提高过氧单硫酸盐活化和单线态氧生成,利用废弃PET塑料衍生的n掺杂碳高效降解四环素

IF 13.2 1区 工程技术 Q1 ENGINEERING, CHEMICAL
Kefu Wang, Changyan Guo, Jiang Li, Yubin Wang, Yage Xing, Peizhi Li, Ziyi Wang, Jide Wang
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引用次数: 0

摘要

为了解决抗生素废水处理带来的技术挑战,克服传统活性炭材料在活性过硫酸盐高级氧化技术中的局限性,本研究旨在开发一种高效、稳定、环保的活性过氧单硫酸盐(PMS)催化材料。理想情况下,多孔碳基复合催化剂可以用富含碳的废聚对苯二甲酸乙二醇酯(PET)作为原料生产。为了提高催化性能和克服这一问题,通常采用非金属掺杂作为改性策略。采用熔融盐辅助法(ZnCl2/NaCl),以酰胺钠(NaNH2)为N源制备了从废弃PET塑料中提取的富氮多孔碳(NPC)。NPC-500样品显示出丰富的孔隙度和更高的表面范围,对20 mg/L的四环素(TC)达到了令人印象深刻的90% %的去除效率。这种效率归因于吸附和催化分解的共同作用。此外,NPC-500具有3-11的广泛pH耐受性,强大的环境耐久性和卓越的循环性能。活性氧(ROS)猝灭实验、电子顺磁共振(EPR)信号、电化学分析和原位表征结果表明,降解机制主要由非自由基过程控制,特别是单线态氧(1O2),其通过表面结合反应配合物介导的电子转移进行。此外,理论分析表明,N的加入增加了静电势,改变了掺杂位点的电子密度分布,从而改善了PMS的吸收和激发。综上所述,本研究提出了一种高效回收塑料废弃物的新方法,为利用富n碳材料处理有机废水提供了技术和理论视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficient degradation of tetracycline via N-doped carbon derived from discarded PET plastics by boosting peroxymonosulfate activation and singlet oxygen generation
To address the technical challenges posed by antibiotic wastewater treatment and overcoming the limitations of traditional carbon materials in activated persulfate advanced oxidation technology, this study aimed to develop an efficient, stable, and eco-friendly catalytic material for activated peroxymonosulfate (PMS). Ideally, porous carbon-based composite catalysts can be produced using carbon-rich waste polyethylene terephthalate (PET) as raw material. To improve the catalytic performance and overcome this problem, non-metallic dopants are often used as a modification strategy. This paper presents the fabrication of nitrogen (N) enriched porous carbon (NPC) derived from discarded PET plastics utilizing a molten-salt-assisted (ZnCl2/NaCl) method, with sodium amide (NaNH2) serving as the N source. The NPC-500 sample showcased an abundant porosity and an elevated surface extent, achieving an impressive 90 % removal efficiency for 20 mg/L of tetracycline (TC). This efficiency was ascribed to the combined action of adsorption and catalytic decomposition. Additionally, the NPC-500 demonstrated a broad pH tolerance range of 3–11, robust environmental durability, and exceptional cycling performance. The results of the reactive oxygen species (ROS) quenching experiments, electron paramagnetic resonance (EPR) signals, electrochemical analyses and in-situ characterizations indicate that the degradation mechanism is primarily governed by non-radical processes, particularly singlet oxygen (1O2), which operates through electron transfer mediated by surface-bound reactive complexes. Furthermore, theoretical analysis shows that the addition of N increases the electrostatic potential and changes the electron density distribution of the doping sites, thereby improving the absorption and stimulation of PMS. In summary, this study proposes a new method for efficient recycling of plastic waste and provides a technical and theoretical perspective for the use of N-rich carbon materials to treat organic wastewater.
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来源期刊
Chemical Engineering Journal
Chemical Engineering Journal 工程技术-工程:化工
CiteScore
21.70
自引率
9.30%
发文量
6781
审稿时长
2.4 months
期刊介绍: The Chemical Engineering Journal is an international research journal that invites contributions of original and novel fundamental research. It aims to provide an international platform for presenting original fundamental research, interpretative reviews, and discussions on new developments in chemical engineering. The journal welcomes papers that describe novel theory and its practical application, as well as those that demonstrate the transfer of techniques from other disciplines. It also welcomes reports on carefully conducted experimental work that is soundly interpreted. The main focus of the journal is on original and rigorous research results that have broad significance. The Catalysis section within the Chemical Engineering Journal focuses specifically on Experimental and Theoretical studies in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. These studies have industrial impact on various sectors such as chemicals, energy, materials, foods, healthcare, and environmental protection.
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