菲
化学
催化作用
选择性
饱和(图论)
空间速度
吸附
位阻效应
金属
兴奋剂
铂金
无机化学
核化学
有机化学
药物化学
物理
数学
光电子学
组合数学
作者
Daocheng Liu,Jieying Jing,Jiu-zhan WANG,Jie Feng,Wenying Li
标识
DOI:10.1016/s1872-5813(21)60128-7
摘要
Limited by the steric hindrance, hydrogenation of the final unsaturated ring in polycyclic aromatic hydrocarbons remains a challenge. In this work, a series of Pt-Ni/NiAlOx catalysts with different Pt doping amounts were synthesized by impregnation method to enhance the adsorption of aromatics, and phenanthrene was served as the model compound. The effects of Pt content on the structure and saturation performance of Pt-Ni/NiAlOx catalysts were systematically investigated. When the saturation reaction was performed at 300°C, 5 MPa and a weight hourly space velocity of 52 h−1, the selectivity of perhydrophenanthrene could be enhanced from 40% over Ni/NiAlOx catalysts to 67% over 0.5Pt-Ni/NiAlOx catalysts with 0.5%Pt loading. Meanwhile, the obvious reaction rate and turnover frequency were also improved from 1.53×10−3mol/(kg·s) and 14.64×10−3s−1 to 1.81×10−3mol/(kg·s) and 22.16×10−3s−1, respectively. This is related to the modified stability of metallic electron-deficient structure of Ni by Pt introduction in phenanthrene hydrogenation, which can promote the adsorption of aromatic hydrocarbons as well as the hydrogenation activity.
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