Synergistic removal of chromium(VI) and tetracycline by porous carbon sponges embedded with MoS2: Performance and radical mechanism of piezoelectric catalysis.

IF 9.4 1区 化学 Q1 CHEMISTRY, PHYSICAL
Journal of Colloid and Interface Science Pub Date : 2025-05-15 Epub Date: 2025-02-06 DOI:10.1016/j.jcis.2025.02.036
Hongwei Xu, Xiaxia Chen, Chao Liu, Mingyang Xu, Chenxi Guo, Yinglong Wang, Zhaoyou Zhu, Fanqing Meng
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引用次数: 0

Abstract

The presence of hexavalent chromium(Ⅵ) Cr(Ⅵ) and antibiotics in the environment can lead to the formation of combined pollutants that are harmful to ecosystems. To address this problem, we synthesized MoS2 embedded in the porous super-hydrophilic polyurethane (PU) sponge and used weak water flow to drive the piezoelectric catalytic synergistic degradation of Cr(Ⅵ) and tetracycline (TC). In this study, the piezoelectric properties of MoS2/PU were confirmed via piezoresponse force microscopy (PFM) and COMSOL multiphysics calculations. Additionally, dynamics experiments, quenching experiments, electron paramagnetic resonance (EPR) spectroscopy, three-dimensional fluorescence excitation-emission matrix (3D-EEM) spectroscopy, and free radical generation rate analysis were conducted to explore the removal performance and mechanisms of MoS2/PU on the TC-Cr(VI) system. The results indicated that the coexistence of the two pollutants promotes the transfer of charge in MoS2/PU, further combined with O2 to produce H2O2 and continued to produce OH. The removal rates of TC and Cr(VI) in the TC-Cr (VI) mixed system at 30 min were 97 % and 94 %, respectively, which were 1.45 and 1.46 times those of the single TC and single Cr(VI) systems, respectively. Finally, potentially vulnerable sites of TC were calculated and analyzed according to density functional theory (DFT). Our results provide a new strategy for improving the degradation efficiency of antibiotics and Cr(VI) metals.

二硫化钼包埋多孔碳海绵协同去除六价铬和四环素:压电催化性能和自由基机制。
环境中六价铬(Ⅵ)、铬(Ⅵ)和抗生素的存在可导致形成对生态系统有害的复合污染物。为了解决这一问题,我们在多孔超亲水性聚氨酯(PU)海绵中合成了MoS2,并利用弱水流驱动压电催化协同降解Cr(Ⅵ)和四环素(TC)。在本研究中,通过压电响应力显微镜(PFM)和COMSOL多物理场计算证实了MoS2/PU的压电性能。此外,通过动力学实验、猝灭实验、电子顺磁共振(EPR)光谱、三维荧光激发发射矩阵(3D-EEM)光谱、自由基生成速率分析等,探讨了MoS2/PU对TC-Cr(VI)体系的去除性能及机理。结果表明,两种污染物的共存促进了MoS2/PU中电荷的转移,进一步与O2结合生成H2O2,并继续生成OH。TC-Cr (VI)混合体系在30 min时对TC和Cr(VI)的去除率分别为97%和94%,分别是单一TC和单一Cr(VI)体系的1.45和1.46倍。最后,根据密度泛函理论(DFT)对TC的潜在易损点进行了计算和分析。我们的研究结果为提高抗生素和Cr(VI)金属的降解效率提供了新的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
16.10
自引率
7.10%
发文量
2568
审稿时长
2 months
期刊介绍: The Journal of Colloid and Interface Science publishes original research findings on the fundamental principles of colloid and interface science, as well as innovative applications in various fields. The criteria for publication include impact, quality, novelty, and originality. Emphasis: The journal emphasizes fundamental scientific innovation within the following categories: A.Colloidal Materials and Nanomaterials B.Soft Colloidal and Self-Assembly Systems C.Adsorption, Catalysis, and Electrochemistry D.Interfacial Processes, Capillarity, and Wetting E.Biomaterials and Nanomedicine F.Energy Conversion and Storage, and Environmental Technologies
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