School of Chemical Engineering & Technology, China University of Mining and Technology, Xuzhou, Jiangsu 221116, PR China.
School of Environment and Spatial Informatics, China University of Mining and Technology, Xuzhou, Jiangsu 221116, PR China.
J Colloid Interface Sci. 2021 Dec;603:685-694. doi: 10.1016/j.jcis.2021.06.142. Epub 2021 Jun 29.
Antibiotics as emerging pollutants in water pose great risks to human health. Due to their persistence in the environment, advanced oxidation processes (AOPs) have been proposed for the degradation of antibiotics. Therefore, developing efficient catalysts for AOPs becomes critical for the removal of antibiotics. Herein, we develop self-propelled CuS-based micromotors (CuS@FeO/Pt) as active heterogenous catalysts for efficient photo-Fenton degradation of antibiotics. Combining the merits of conventional heterogenous and homogenous catalysts, the prepared micromotors are easy to recycle and free of secondary pollution risks, while demonstrating high degradation efficiency due to self-induced intensification of mass transfer via autonomous motion and microbubble generation. The HO in the Fenton reagents can serve as the fuel for the micromotors to drive their self-propulsion by bubbles generated from catalytic decomposition of HO by the platinum layer. The dual-stimuli-responsiveness of the micromotors to magnetic field and light irradiation allows multi-modes of propulsion and guidance in different systems. The efficient photothermal effect of CuS enables the micromotors to achieve collective phototactic motion toward light, whereas magnetic responsiveness facilitates the recovery and collection of the micromotors. The synergistic effect of CuS and FeO NPs in HO under visible light irradiation generates a large amount of OH· and ·O to effectively degrade tetracycline within several minutes. With these advantages, the dual-stimuli-responsive CuS-based micromotors provide a new strategy for enhanced degradation of antibiotics in water purification applications.
抗生素作为水中新兴的污染物,对人类健康构成了巨大的威胁。由于它们在环境中的持久性,高级氧化工艺(AOPs)已被提议用于抗生素的降解。因此,开发用于 AOPs 的高效催化剂对于去除抗生素至关重要。在此,我们开发了自推进的 CuS 基微马达(CuS@FeO/Pt)作为用于抗生素的高效光芬顿降解的活性非均相催化剂。结合传统非均相和均相催化剂的优点,所制备的微马达易于回收,并且没有二次污染的风险,同时由于通过自诱导的质量传递强化和微气泡生成而表现出高的降解效率。Fenton 试剂中的 HO 可以作为微马达的燃料,通过铂层催化分解 HO 产生的气泡来驱动其自推进。微马达对磁场和光辐射的双重刺激响应允许在不同的系统中进行多种推进和导向模式。CuS 的高效光热效应使微马达能够实现对光的集体趋光运动,而磁性响应则有利于微马达的回收和收集。在可见光照射下,CuS 和 FeO NPs 在 HO 中的协同作用产生大量的 OH·和·O,可在几分钟内有效降解四环素。具有这些优点,双刺激响应的 CuS 基微马达为水净化应用中增强抗生素的降解提供了一种新策略。