脱氢
双金属片
催化作用
选择性
化学
空间速度
沸石
丙烷
铂金
无机化学
锌
有机化学
作者
Qiming Sun,Ning Wang,Qiyuan Fan,Lei Zeng,Álvaro Mayoral,Shu Miao,Ruoou Yang,Zheng Jiang,Wei Zhou,Jichao Zhang,Tianjun Zhang,Jun Xu,Peng Zhang,Jun Cheng,Dongchun Yang,Ran Jia,Lin Li,Qinghong Zhang,Ye Wang,Osamu Terasaki
标识
DOI:10.1002/anie.202003349
摘要
Propane dehydrogenation (PDH) has great potential to meet the increasing global demand for propylene, but the widely used Pt-based catalysts usually suffer from short-term stability and unsatisfactory propylene selectivity. Herein, we develop a ligand-protected direct hydrogen reduction method for encapsulating subnanometer bimetallic Pt-Zn clusters inside silicalite-1 (S-1) zeolite. The introduction of Zn species significantly improved the stability of the Pt clusters and gave a superhigh propylene selectivity of 99.3 % with a weight hourly space velocity (WHSV) of 3.6-54 h-1 and specific activity of propylene formation of 65.5 mol C3H6 gPt-1 h-1 (WHSV=108 h-1 ) at 550 °C. Moreover, no obvious deactivation was observed over PtZn4@S-1-H catalyst even after 13000 min on stream (WHSV=3.6 h-1 ), affording an extremely low deactivation constant of 0.001 h-1 , which is 200 times lower than that of the PtZn4/Al2 O3 counterpart under the same conditions. We also show that the introduction of Cs+ ions into the zeolite can improve the regeneration stability of catalysts, and the catalytic activity kept unchanged after four continuous cycles.
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