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Selective hydrogenation of mixed alkyne/alkene streams at elevated pressure over a palladium sulfide catalyst
Journal of Catalysis ( IF 7.3 ) Pub Date : 2017-09-23 , DOI: 10.1016/j.jcat.2017.09.004
Alan J. McCue , Antonio Guerrero-Ruiz , Carolina Ramirez-Barria , Inmaculada Rodríguez-Ramos , James A. Anderson

The Pd4S phase of palladium sulfide is known to be a highly selective alkyne hydrogenation catalyst at atmospheric pressure. Results presented here demonstrate that high selectivity can be retained at the elevated pressures required in industrial application. For example, in a mixed acetylene/ethylene feed, 100% conversion of acetylene was attained with a selectivity to ethylene in excess of 80% at 18 bar pressure. Similarly, almost 85% selectivity can be obtained with mixed C3 feeds containing methyl acetylene, propadiene, propylene and propane at 18 bar pressure. Using a low loaded sample (0.1 wt% Pd) it was possible to estimate the TOF to be 27 s−1. High selectivity was related to the crystal structure of Pd4S with the unique spatial arrangement thought to favour Pd atoms acting in isolation from one another. Based on these results, it is proposed that this catalyst could be a potential replacement for PdAg alloys currently used by industry.



中文翻译:

硫化钯催化剂在高压下选择性混合氢化炔烃/烯烃

已知在大气压下硫化钯的Pd 4 S相是高度选择性的炔烃加氢催化剂。此处给出的结果表明,在工业应用中所需的高压下可以保持高选择性。例如,在乙炔/乙烯混合进料中,在18巴的压力下,乙炔的转化率达到了100%,对乙烯的选择性超过80%。类似地,在18 bar压力下,使用含有甲基乙炔,丙二烯,丙烯和丙烷的混合C3进料,可以获得近85%的选择性。使用低负载样品(0.1 wt%Pd),可以估计TOF为27 s -1。高选择性与Pd 4的晶体结构有关具有独特空间排列的S被认为有利于Pd原子彼此独立地起作用。基于这些结果,提出该催化剂可以潜在地替代当前工业上使用的PdAg合金。

更新日期:2017-09-23
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