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Cu-Mo/C催化油酸甲酯选择性加氢脱氧制备生物柴油

Preparation of Biodiesel by Selective Hydrodeoxygenation Methyl Oleate over Cu-Mo/C Catalyst

  • 摘要: 使用四水合钼酸铵和三水合硝酸铜制备了Cu-Mo/C, 并将其用作油酸甲酯选择性加氢脱氧反应的催化剂。利用X射线衍射(XRD)、X射线光电子能谱(XPS)和电子顺磁共振波谱(EPR)对催化剂进行表征, 并探讨了Cu-Mo/C催化油酸甲酯制备生物柴油的较佳工艺和Cu-Mo/C的催化性能。研究结果显示: Cu的加入促进了Mo/C催化剂的形成, 催化剂中的Mo2C组分和MoO2组分共同作用, MoO2组分中的氧空位可以优先吸附底物中的C=O键, 随后Mo2C组分对其进行加氢脱氧, 避免了C=C键发生加氢反应, 实现了高催化活性和不饱和烃选择性加氢脱氧的优异性能。在反应温度280 ℃, 氢气压力2.5 MPa, 反应时间3 h的条件下油酸甲酯转化率达到98.8%, 不饱和烃选择性为40.2%。Cu-Mo10/C催化活性与贵金属Pd和商业催化剂Mo/C相当, 但不饱和烃选择性更高, 且具有良好的稳定性。

     

    Abstract: The Cu-Mo/C catalyst was prepared with ammonium molybdate tetrahydrate and copper nitrate trihydrate, and used for the selective hydrodeoxygenation reaction of methyl oleate. The catalysts were characterized by X-ray diffraction, X-ray diffraction photoelectron spectroscopy and electron paramagnetic resonance spectroscopy. The optimal process for the preparation of biodiesel from methyl oleate catalyzed by Cu-Mo/C and the catalytic performance of Cu-Mo/C were investigated. The results of the study showed that the addition of Cu promoted the formation of Mo/C catalyst and the Mo2C and MoO2 component in the catalyst worked together. The oxygen vacancies on the MoO2 component could preferentially adsorb the C=O bond in the substrate and then Mo2C component hydrodeoxygenated it, avoiding the hydrogenation of C=C bond. The excellent performance of catalyst and the selectivity of unsaturated hydrocarbons were achieved. The conversion rate of methyl oleate reached 98.8%, and the selectivity of unsaturated hydrocarbons was 40.2% at reaction temperature of 280 ℃, hydrogen pressure of 2.5 MPa and reaction time of 3 h. The catalytic activity of Cu-Mo10/C was comparable to the noble metal Pd and commercial Mo/C catalysts, while the unsaturated hydrocarbon selectivity was higher as well as the good stability.

     

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