通过无氟 Ti3C2Tx-CoFe2O4 水凝胶珠实现抗生素降解的连续过氧单磺酸盐活化:性能、机理和应用

Feng Wang, Yaru Zhang, Yiyin Peng, Wenyu Xiao, Wenchao Yu, Hui Wang, Zhaoyong Bian
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引用次数: 0

摘要

本研究探索了通过层状无氟 TiCT 和 CoFeO 纳米微球之间的快速电子传递,高效、稳定、连续地处理含抗生素废水的方法。这些材料被合成为与海藻酸钠交联的水凝胶珠,因此具有很高的反应活性和稳定性。实验和 DFT 计算证实,Ff-TiCT-CoFeO 催化剂通过快速电子传递和 Ff-TiCT-CoFeO-PMS* 物种的形成,促进了过氧化单磺酸盐(PMS)的活化。Ff-TiCT-CoFeO 催化剂上 S-O 键的裂解被确定为产生单线态氧 (O) 的主要机制。在连续流动系统中,抗生素(如磺胺甲噁唑 (SMX))的降解效率保持在 96.9% 以上,金属浸出率超低(<1.3 μg-L,72 小时)。这项研究为 PMS 活化技术在抗生素降解方面的实际应用提供了重要启示,为废水处理提供了一种可持续的解决方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Continuous peroxymonosufate activation for antibiotics degradation via fluorine-free-Ti3C2Tx-CoFe2O4 hydrogel beads: Performance, mechanism and application
This study explored the efficient, stable, and continuous treatment of antibiotic-containing wastewater through rapid electron transfer between layered fluorine-free TiCT and CoFeO nanomicrospheres. These materials were synthesized into hydrogel beads crosslinked with sodium alginate, resulting high reactivity and stability. Ff-TiCT-CoFeO catalyst facilitated peroxymonosufate (PMS) activation through rapid electron transfer and the formation of Ff-TiCT-CoFeO-PMS* species, as confirmed by experiments and DFT calculations. The cleavage of the S-O bond on Ff-TiCT-CoFeO catalyst identified as the primary mechanism for the generation of singlet oxygen (O) In a continuous flow system, the degradation efficiency of antibiotics, such as sulfamethoxazole (SMX), remained above 96.9 % with ultra-low metal leaching (<1.3 μg·L, 72 h). This research provides significant insights into the practical application of PMS activation for antibiotic degradation, offering a sustainable solution for wastewater treatment.
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