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Fabrication of a Z-scheme Bi2MoO6/NiFe layered double hydroxide heterojunction for the visible light-driven degradation of tetracycline antibiotics
Journal of Water Process Engineering ( IF 6.3 ) Pub Date : 2024-01-17 , DOI: 10.1016/j.jwpe.2024.104813
Abinaya Murugan Bharathi , Preeyanghaa Mani , Bernaurdshaw Neppolian , Han Sen Soo , Tamilarasan Krishnamurthi

Heterojunction catalysts offer promising potential for efficient and sustainable remediation of polluted environments. In this study, Z-scheme Bi2MoO6/NiFe layered double hydroxide (BMO/NiFe) heterojunction catalysts were synthesized using solvothermal process. The surface morphology, crystalline structure, and photochemical characteristics of the synthesized photocatalyst were analyzed by several spectroscopic and electron microscopy methods. BMO, NiFe and BMO/NiFe were efficiently utilized for tetracycline (TC) antibiotics degradation under visible light irradiation. The experimental findings suggest that the BMO/NiFe15 heterojunction catalyst greatly enhances the TC degradation rate to 95 % under 300 W visible light irradiation for 120 min. The rate constant of 0.0219 min−1 indicates a rapid degradation process following pseudo first-order kinetics. Furthermore, the effect of active free radicals, the recyclability of the catalyst and the photocatalytic degradation mechanism of TC were proposed. This novel method opens up possibilities for creating advanced photocatalysts, which can effectively degrade TC in water bodies, addressing the urgent need for its removal from aquatic environments. The present work serves as a primary pathway to design and develop efficient Bi2MoO6-based direct Z-scheme photocatalysts with promising applications in simultaneous wastewater degradation with hydrogen evolution.



中文翻译:

Z型Bi2MoO6/NiFe层状双氢氧化物异质结的制备用于可见光驱动的四环素抗生素降解

异质结催化剂为污染环境的高效和可持续修复提供了广阔的前景。本研究采用溶剂热法合成了Z型Bi 2 MoO 6 /NiFe层状双氢氧化物(BMO/NiFe)异质结催化剂。通过多种光谱和电子显微镜方法分析了合成光催化剂的表面形貌、晶体结构和光化学特性。BMO 、NiFe 和 BMO/NiFe 可有效用于可见光照射下的四环素 (TC) 抗生素降解。实验结果表明,BMO/NiFe 15异质结催化剂在300 W可见光照射120 min下,TC降解率大大提高至95%。0.0219 min -1的速率常数表明遵循伪一级动力学的快速降解过程。此外,还提出了活性自由基的影响、催化剂的可回收性以及TC的光催化降解机理。这种新颖的方法为制造先进的光催化剂开辟了可能性,它可以有效降解水体中的TC,解决从水生环境中去除TC的迫切需求。目前的工作是设计和开发高效 Bi 2 MoO 6基直接 Z 型光催化剂的主要途径,在废水同时降解和析氢方面具有广阔的应用前景。

更新日期:2024-01-18
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