Cui Kang-Ping, He Yu-Ying, Xu Kai-Jie, Zhang Yu, Chen Chang-Bin, Xu Zheng-Jiang, Chen Xing
School of Resource and Environmental Engineering, Hefei University of Technology, Hefei 230009, China.
Key Lab of Aerospace Structural Parts Forming Technology and Equipment of Anhui Province, Institute of Industry and Equipment Technology, Hefei University of Technology, Hefei 230009, China.
Nanomaterials (Basel). 2022 Feb 28;12(5):811. doi: 10.3390/nano12050811.
In this work, the combination of high surface area diatomite with Fe and Cu bimetallic MOF material catalysts (FeCu(BDC)@DE) were synthesized by traditional solvothermal method, and exhibited efficient degradation performance to tetracycline hydrochloride (TC). The degradation results showed: Within 120 min, about 93% of TC was degraded under the optimal conditions. From the physical-chemical characterization, it can be seen that Fe and Cu play crucial roles in the reduction of Fe because of their synergistic effect. The synergistic effect can not only increase the generation of hydroxyl radicals (•OH), but also improve the degradation efficiency of TC. The Lewis acid property of Cu achieved the pH range of reaction system has been expanded, and it made the material degrade well under both neutral and acidic conditions. Loading into diatomite can reduce agglomeration and metal ion leaching, thus the novel catalysts exhibited low metal ion leaching. This catalyst has good structural stability, and less loss of performance after five reaction cycles, and the degradation efficiency of the material still reached 81.8%. High performance liquid chromatography-mass spectrometry was used to analyze the degradation intermediates of TC, it provided a deep insight of the mechanism and degradation pathway of TC by bimetallic MOFs. This allows us to gain a deeper understanding of the catalytic mechanism and degradation pathway of TC degradation by bimetallic MOFS catalysts. This work has not only achieved important progress in developing high-performance catalysts for TC degradation, but has also provided useful information for the development of MOF-based catalysts for rapid environmental remediation.
在这项工作中,通过传统的溶剂热法合成了具有高比表面积的硅藻土与铁和铜双金属MOF材料催化剂(FeCu(BDC)@DE),其对盐酸四环素(TC)表现出高效的降解性能。降解结果表明:在120分钟内,在最佳条件下约93%的TC被降解。从物理化学表征可以看出,由于铁和铜的协同作用,它们在铁的还原中起着关键作用。这种协同作用不仅可以增加羟基自由基(•OH)的产生,还能提高TC的降解效率。铜的路易斯酸性扩大了反应体系的pH范围,使得该材料在中性和酸性条件下都能很好地降解。负载到硅藻土中可以减少团聚和金属离子浸出,因此这种新型催化剂表现出低金属离子浸出。该催化剂具有良好的结构稳定性,经过五个反应循环后性能损失较小,材料的降解效率仍达到81.8%。采用高效液相色谱-质谱联用分析TC的降解中间体,深入了解了双金属MOF对TC的降解机理和降解途径。这使我们对双金属MOF催化剂降解TC的催化机理和降解途径有了更深入的理解。这项工作不仅在开发用于TC降解的高性能催化剂方面取得了重要进展,也为基于MOF的快速环境修复催化剂的开发提供了有用信息。