Yongle Zhang, Yingyi Tu, Yunying Huo, Guang Pan, Qiao Zhang, Zhiting Liu, Guangxing Yang and Feng Peng
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引用次数: 0
摘要
电化学催化氧化5-羟甲基糠醛(HMF)生成2,5-呋喃二羧酸(FDCA)等高价值产品已成为研究热点。本文采用经济高效的过渡金属ε-MnO2催化剂,在酸性环境下电催化HMF氧化。结果表明,在60°C、0.5 M H2SO4、1.6 V (vs. RHE)条件下,HMF转化率为92.95%,FDCA收率为23.03%。此外,研究概述了HMF的氧化途径,其过程顺序为:HMF→DFF→FFCA→FDCA。各氧化阶段的表观活化能分别为25.52、22.12和16.21 kJ mol−1。此外,研究结果表明,HMF的电催化氧化活性与ε-MnO2的平均表面氧化态之间存在良好的关系。
Electrocatalytic oxidation of 5-hydroxymethylfurfural by MnO2 with tunable surface oxidation states†
The electrochemical catalytic oxidation of 5-hydroxymethylfurfural (HMF) to generate high-value products like 2,5-furandicarboxylic acid (FDCA) has become a prominent research interest. In this work, an economical and efficient transition metal ε-MnO2 catalyst was used to electrocatalyze the oxidation of HMF in acidic environments. The results revealed a highly efficient HMF conversion rate of 92.95% and a FDCA yield of 23.03% under the specific conditions of 60 °C, 0.5 M H2SO4 and 1.6 V (vs. RHE). Furthermore, the study outlined the oxidation pathway for HMF, which progresses through the following sequence: HMF → DFF → FFCA → FDCA. The apparent activation energies associated with each oxidation stage were found to be 25.52, 22.12 and 16.21 kJ mol−1, respectively. Moreover, the findings indicated a favorable relationship between the electrocatalytic oxidation activity of HMF and the average surface oxidation state of ε-MnO2.
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