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Selective hydrogenolysis of 5-hydroxymethylfurfural to 2,5-dimethylfuran over Co_3O_4 catalyst by controlled reduction

查看全文 作  者:Dan [1,2]Li;Qiying [3,2]Liu;Changhui [3,4,2]Zhu;Haiyong [3,4,2]Wang;Chunhua [3,2]Cui;Chenguang [3,2]Wang;Longlong [3,2]Ma 高影响力作者 机构地区:[1]Nano Science and Technology Institute, University of Science and Technology of China;[2]Guangdong Provincial Key Laboratory of New and Renewable Energy Research and Development;[3]CAS Key Laboratory of Renewable Energy, Guangzhou Institute of Energy Conversion, Chinese Academy of Sciences;[4]University of Chinese Academy of Sciences高影响力机构 出  处:《Journal of Energy Chemistry》索引2019年第28卷第3期,共8页高影响力期刊 基  金:financially supported by the National Natural Science Foundation of China(51576199 and 51536009);the Natural Science Fund of Guangdong Province(2017A030308010) 摘  要:2,5-dimethyfuran(DMF), which is produced from 5-hydroxymethyfurfural(HMF) by hydrodeoxygenation(HDO), is a high quality fuel due to the high heating value, the high octane number and the suitable boiling point. Selective hydrogenation of HMF into liquid fuel DMF has been widely researched. In this paper, Co_3O_4 catalyst was prepared by co-precipitation and was reduced at different temperatures to form Co–CoO_x catalysts. The characterization of catalysts was tested by XRD, TEM, XPS, TPR, BET and NH3-TPD.Co–CoO_x possessed a high amount of Co metal and CoO_x acidic sites, wherein Co worked as the active hydrogenation sites and CoO_x acted as the acid promoter to facilitate the selective HDO of HMF to DMF.The synergistic effect of Co–CoO_x is the key for HDO of HMF, obtaining 83.3% of DMF yield at 170 °C, 12 h and the reduction temperature of 400 °C. This method not only saves the catalyst cost, but also promotes the utilization of biomass energy. 关 键 词:HMF DMF CO3O4 CATALYST HYDROGENOLYSIS
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