催化作用
材料科学
氧化物
化学工程
蒽醌
选择性
阳极氧化
过氧化氢
阳极
纳米颗粒
氢
扩散
无机化学
化学
纳米技术
有机化学
复合材料
冶金
物理化学
电极
铝
工程类
物理
热力学
作者
Runrun Hong,Junting Feng,Yufei He,Dianqing Li
标识
DOI:10.1016/j.ces.2015.04.003
摘要
Anodic alumina oxide (AAO) supports with different pore sizes and depths were controllable prepared by a two-step low-potential anodizing process. The prepared AAO supports with θ-ring shape were utilized to prepare supported Pd catalysts by impregnation method for the first time. The catalytic performance of the Pd/[email protected] catalysts were investigated in the catalytic hydrogenation of 2-ethylanthraquinone (eAQ) to 2-ethylanthrahydroquinone, a key step in the anthraquinone process for the manufacture of hydrogen peroxide. Compared with Pd supported on spherical Al2O3 catalyst, Pd/[email protected] catalysts showed much higher anthraquinone hydrogenation activity and preferable selectivity due to the highly ordered array of cylindrical shaped pores, short diffusion distance and confinement effect of the AAO supports. Furthermore, the effect of pore size and depth to the catalytic performance towards hydrogenation of eAQ has also been studied. Pd nanoparticles supported on AAO support with 24.5 nm pore size and 18 μm depth exhibited the best catalytic performance towards hydrogenation of eAQ.
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