催化作用
马来酸酐
琥珀酸酐
钴
解吸
镍
选择性
X射线光电子能谱
材料科学
化学
无机化学
吸附
热脱附光谱法
核化学
高分子化学
化学工程
有机化学
共聚物
聚合物
工程类
作者
Mingrong Chen,Xuan Meng,Naiwang Liu,Li Shi
出处
期刊:Fuel
[Elsevier BV]
日期:2022-08-31
卷期号:331: 125520-125520
被引量:9
标识
DOI:10.1016/j.fuel.2022.125520
摘要
In order to prepare supported catalysts with low-metal loading, a series of NiCo/Clay catalysts were prepared and used in the hydrogenation of maleic anhydride. The hydrogenation reaction was carried out in a fixed-bed for 8 h with reaction pressure = 1 MPa, reaction temperature = 180 °C, molar ratio of H2: maleic anhydride = 50, WHSV = 2 h−1. Ni4Co1/Clay (loaded 3 wt%Ni and 0.75 wt%Co) can maintain no obvious catalyst deactivation within 8 h. The overall conversion of maleic anhydride is not less than 95 %, and the selectivity of succinic anhydride is up to 100 %. N2 adsorption–desorption characterization, X-ray diffraction, temperature-programmed reduction, temperature-programmed desorption, X-ray photoelectron spectroscopy and transmission electron microscopy were performed to verify the changes in catalyst morphology, active species, reduction performance and hydrogenation activity after adding Co as a promoter. With the addition of Co additive, the distribution of active sites on the carrier is more uniform, the grain size of active metal becomes smaller and the reduction temperature decreases. The addition of Co not only increased the active center of the catalyst but also effectively avoided the catalyst's deactivation.
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