烟气脱硫
催化作用
化学
猝灭(荧光)
氧化磷酸化
化学计量学
化学工程
有机化学
生物化学
物理
量子力学
工程类
荧光
作者
Xue Lu,Jingfang Li,Liye Liang,Guangming Li
出处
期刊:Fuel
[Elsevier]
日期:2024-01-11
卷期号:362: 130849-130849
被引量:4
标识
DOI:10.1016/j.fuel.2023.130849
摘要
Deep desulfurization with high-efficiency is imperia for environmental demands with increasing stringent standard of sulfur content in fuels. To develop high efficiency heterogeneous catalyst for aerobic oxidative desulfurization (AODS) of fuel, an Anderson-type CoMo6-2NH2 (POM) as active site, which was considered to be very effective in catalyzing the activation of O2, was successfully anchored on the sub-stoichiometric ECOF as a carrier by Schiff-base condensation reaction between –NH2 groups in CoMo6-2NH2 and –CHO groups in ECOF. The anchoring of CoMo6-2NH2 on ECOF by covalent bond resulted in the heterogenization of CoMo6-2NH2 enabled CoMo6-2NH2@ECOF to be recyclable during the AODS process. When CoMo6-2NH2@ECOF was applied as catalyst for AODS of fuel with surfactant (OTAC) under O2, it exhibited excellent catalytic activity with almost 100 % removal rates under 95 °C for 6 h. Moreover, the catalyst can be recycled 7 times without significant loss of catalytic activity. Further, the structure-activity relationship was investigated and the reaction mechanism of AODS of fuel was verified by ESR, XPS analysis and selective quenching experiments.
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