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Hydrogenation of alkyl-anthraquinone over hydrophobically functionalized Pd/SBA-15 catalysts

机译:疏水官能化的Pd / SBA-15催化剂上烷基蒽醌的加氢

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Organosilane-functionalized mesoporous silica SBA-15 was prepared by the co-condensation method and then applied as a support of Pd catalysts for hydrogenation of 2-alkyl-anthraquinone (AQ, alkyl = ethyl, tert -butyl and amyl). The as-prepared Pd catalysts were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, thermogravimetric analysis, N _(2) adsorption–desorption, zeta potential, water contact angles measurement and transmission electron microscopy. By extending the pre-hydrolysis time of the silica source, the content of functional groups in the catalysts slightly increases. However, there is an initial increase in zeta potential and water contact angles up to a maximum at 2 h, followed by a decrease as the pre-hydrolysis time was further prolonged. The hydrophobicity created by organic functionalization has positive effects on AQ hydrogenation. The catalyst with the highest hydrophobicity exhibits the highest catalytic activity, with increments of 33.3%, 60.0% and 150.0% for hydrogenation of ethyl-, tert -butyl- and amyl-anthraquinone compared with the unfunctionalized one.
机译:通过共缩合方法制备有机硅烷官能化的介孔二氧化硅SBA-15,然后将其用作Pd催化剂的载体,用于氢化2-烷基蒽醌(AQ,烷基=乙基,叔丁基和戊基)。通过X射线衍射,傅立叶变换红外光谱,热重分析,N_(2)吸附-脱附,Zeta电位,水接触角测量和透射电子显微镜对所制备的Pd催化剂进行了表征。通过延长二氧化硅源的预水解时间,催化剂中官能团的含量略有增加。但是,zeta电位和水接触角最初会增加,在2 h时达到最大值,然后随着预水解时间的进一步延长而降低。有机官能化产生的疏水性对AQ加氢有积极影响。具有最高疏水性的催化剂表现出最高的催化活性,与未官能化的乙基,叔丁基和戊基蒽醌的氢化相比,其增量分别为33.3%,60.0%和150.0%。

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