催化作用
电子顺磁共振
化学
X射线光电子能谱
核化学
降级(电信)
罗丹明B
傅里叶变换红外光谱
猝灭(荧光)
反应速率常数
动力学
化学工程
光催化
荧光
有机化学
核磁共振
电信
物理
量子力学
计算机科学
工程类
作者
Yiqun Chen,Xiaori Huang,Dezhi Sun,Hongchao Ma,Guowen Wang,Chun Ma,Jun Hao
标识
DOI:10.1016/j.seppur.2021.119468
摘要
In this study, the Fe3O4/Co3[Co(CN)6]2 composite catalyst was synthesized by co-precipitation method. The morphology and the structure of Fe3O4/Co3[Co(CN)6]2 composites were characterized by XRD, FTIR, SEM, TEM, EDS, XPS, VSM. The results showed that the removal rate of RhB (10 mg/L) reached 99.5% in 40 min in the 0.4-Fe3O4/Co3[Co(CN)6]2 (200 mg/L) + PMS (50 mg/L) system with a pseudo first-order degradation rate constant (k) of 0.121 min−1 , which is nearly 2.16 times of that (0.0561 min−1) in the Co3[Co(CN)6]2 + PMS system and 18.9 times of that (0.0064 min−1) in the Fe3O4 + PMS system. The observed synergistic catalysis between Fe3O4 and Co3[Co(CN)6]2 in Fe3O4/Co3[Co(CN)6]2 enhanced the degradation of RhB. The electron paramagnetic resonance (EPR) analysis and quenching experiment indicated that SO4− and OH played important roles in the degradation process of RhB. A synergistic catalytic mechanism of PMS activation by Fe3O4/Co3[Co(CN)6]2, which mainly involves the enhanced Co2+/Co3+ cycle by Fe2+ donated electrons, was proposed. In summary, owing to its easy preparation, excellent catalytic activity, and reusability, the Fe3O4/Co3[Co(CN)6]2 composite catalyst is a good candidate for remediation of contaminated water.
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