Highly efficient microwave-assisted Fenton degradation of metacycline using pine-needle-like CuCo2O4 nanocatalyst

羟基化 催化作用 化学 反应速率常数 活化能 核化学 羟基自由基 降级(电信) 动力学 激进的 有机化学 电信 计算机科学 物理 量子力学
作者
Yi Qi,Yuqing Mei,Jiaqi Li,Tongjie Yao,Yang Yang,Wenjie Jia,Xin Tong,Jie Wu,Baifu Xin
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:373: 1158-1167 被引量:112
标识
DOI:10.1016/j.cej.2019.05.097
摘要

Abstract The heterogeneous Fenton reaction was a powerful technique for degrading organics in wastewater. However, it usually took a long time to meet efficiency requirement. To solve this problem, herein, pine-needle-like CuCo2O4 was prepared and applied as a catalyst in a microwave-assisted Fenton reaction (MAFR) towards antibiotic metacycline (MTC). The optimized degradation condition was 500 μL of H2O2, 10.0 mg of catalyst, 50 mg/L of MTC, and 90 °C of temperature, under which MTC was degraded within 4.0 min. Dynamics data revealed that the activation energy of MAFR was 17.3 kJ/mol, which was much lower than that of the corresponding heterogeneous Fenton reaction (52.2 kJ/mol). Owing to the synergistic effect of combining Cu(II)/Cu(I) and Co(III)/Co(II) sites, the reaction rate constant of CuCo2O4 nanoneedles (7.2 × 10−1 min−1) was much higher than that of the CuO (1.3 × 10−1 min−1), Co3O4 (2.2 × 10−1 min−1), and mixed CuO + Co3O4 (1.5 × 10−1 min−1) references. CuCo2O4 nanoneedles could be easily separated from the reaction solution, and their degradation efficiency remained 86.4% after the 5th cycle. To study the catalytic mechanism, radical trapping experiments were performed, and the results revealed that OH played a dominating role in the degradation process. A possible degradation pathway of MTC was investigated, and it was determined that hydroxylation, de-alkylation, de-hydroxylation, and ring-opening reactions were involved for final inorganic molecules.
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