溶胶-凝胶法制备无负载Ni-Mo复合氧化物加氢脱氧催化剂

D. Yan, W. Xin, Hou Kai-hu
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引用次数: 0

摘要

以柠檬酸为配合剂,采用溶胶-凝胶法制备了无负载Ni-Mo复合氧化物催化剂。采用n2吸附-脱附、x射线衍射(XRD)和程序升温脱附(NH3-TPD)对催化剂进行了表征。以乙酸和苯酚为探针化合物,重点考察了Mo/Ni摩尔比和反应温度对催化剂加氢脱氧活性的影响。结果表明,溶胶-凝胶法制备的催化剂具有较高的比表面积和双介孔结构。催化剂中存在XRD测定的- Â-NiMoO3相。当Mo/Ni摩尔比在0.0 ~ 0.8之间时,催化剂的孔体积、比表面积、中等强酸性和加氢脱氧活性不是Mo/Ni摩尔比的单调递增函数。Mo/Ni比为0.6的催化剂表现出最高的加氢脱氧活性。在0.3MPa下,苯酚在210℃下的脱氧率为99.0%,醋酸在270℃下的脱氧率为99.9%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unsupported Ni-Mo Composite Oxide Catalysts Prepared by Sol-gel Method for Hydrodeoxygenation
Unsupported Ni-Mo composite oxide catalysts were successfully prepared by the sol-gel method with citric acid as a complex agent. The catalysts were characterized using N2adsorption-desorption, X-ray diffraction (XRD) and temperature programmed desorption (NH3-TPD). The effects of Mo/Ni molar ratio and reaction temperature on the hydrodeoxygenation activity of the catalysts were investigated emphatically using acetic acid and phenol as probe compounds. The results showed that the catalysts prepared by the sol-gel method can possess higher specific surface area and the double mesoporous structure. The ¦Â-NiMoO3 phase determined by XRD was existed in the catalysts. For Mo/Ni molar ratios between 0.0 ~ 0.8, the pore volume, the specific surface area, the medium strong acidity and hydrodeoxygenation activity of the catalyst are not monotonically increasing functions of Mo/Ni ratio. The catalyst with Mo/Ni ratio of 0.6 exhibited the highest hydrodeoxygenation activity. At 0.3MPa, the deoxygenation percentage of the phenol was 99.0% at 210¡æand 99.9% at 270¡æ for the acetic acid, respectively.
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