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3D自支撑MoS/MXene纳米复合物增强过二硫酸盐活化以完全降解难降解四环素

Enhancement of Peroxydisulfate Activation for Complete Degradation of Refractory Tetracycline by 3D Self-Supported MoS/MXene Nanocomplex.

作者信息

Song Yuxia, Chen Runhua, Li Shihai, Yu Shali, Ni Xiaoli, Fang Minglong, Xie Hanyun

机构信息

College of Life and Environmental Sciences, Central South University of Forestry and Technology, Changsha 410004, China.

出版信息

Nanomaterials (Basel). 2024 Apr 30;14(9):786. doi: 10.3390/nano14090786.

Abstract

Antibiotic abuse, particularly the excessive use of tetracycline (TC), a drug with significant environmental risk, has gravely harmed natural water bodies and even posed danger to human health. In this study, a three-dimensional self-supported MoS/MXene nanohybrid with an expanded layer spacing was synthesized via a facile one-step hydrothermal method and used to activate peroxydisulfate (PDS) for the complete degradation of TC. The results showed that a stronger •OH signal was detected in the aqueous solution containing MoS/MXene, demonstrating a superior PDS activation effect compared to MoS or TiCT MXene alone. Under the conditions of a catalyst dosage of 0.4 g/L, a PDS concentration of 0.4 mM, and pH = 5.0, the MoS/MXene/PDS system was able to fully eliminate TC within one hour, which was probably due to the presence of several reactive oxygen species (ROS) (•OH, SO, and O) in the system. The high TC degradation efficiency could be maintained under the influence of various interfering ions and after five cycles, indicating that MoS/MXene has good anti-interference and reusability performance. Furthermore, the possible degradation pathways were proposed by combining liquid chromatography-mass spectrometry (LC-MS) data and other findings, and the mechanism of the MoS/MXene/PDS system on the degradation process of TC was elucidated by deducing the possible mechanism of ROS generation in the reaction process. All of these findings suggest that the MoS/MXene composite catalyst has strong antibiotic removal capabilities with a wide range of application prospects.

摘要

抗生素滥用,尤其是具有重大环境风险的四环素(TC)的过度使用,已严重损害天然水体,甚至对人类健康构成威胁。在本研究中,通过简便的一步水热法合成了一种具有扩大层间距的三维自支撑MoS/MXene纳米杂化物,并用于活化过二硫酸盐(PDS)以实现TC的完全降解。结果表明,在含有MoS/MXene的水溶液中检测到更强的•OH信号,表明与单独的MoS或TiCT MXene相比,其具有优异的PDS活化效果。在催化剂用量为0.4 g/L、PDS浓度为0.4 mM和pH = 5.0的条件下,MoS/MXene/PDS体系能够在一小时内完全去除TC,这可能是由于体系中存在多种活性氧物种(ROS)(•OH、SO和O)。在各种干扰离子的影响下以及经过五个循环后,仍可保持较高的TC降解效率,表明MoS/MXene具有良好的抗干扰和可重复使用性能。此外,结合液相色谱 - 质谱(LC-MS)数据和其他研究结果提出了可能的降解途径,并通过推导反应过程中ROS生成的可能机制阐明了MoS/MXene/PDS体系对TC降解过程的作用机制。所有这些研究结果表明,MoS/MXene复合催化剂具有强大的抗生素去除能力,具有广泛的应用前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a77/11085324/dd2e7548da99/nanomaterials-14-00786-g001.jpg

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