Hollow silicalite-1 encapsulated nickel nanoparticles as highly stable catalysts in maleic anhydride hydrogenation

被引:0
|
作者
Zhuang, Jianguo [1 ]
Guan, Yingjie [1 ]
Li, Bihong [2 ]
Wu, Haidan [1 ]
Yu, Jisheng [1 ]
Yan, Siyan [3 ]
Su, Zhaojie [1 ]
Wang, Tianyun [1 ]
Zhu, Xuedong [1 ]
Yang, Fan [3 ]
机构
[1] East China Univ Sci & Technol, Engn Res Ctr Large Scale Reactor Engn & Technol, Minist Educ, Shanghai 200237, Peoples R China
[2] East China Univ Sci & Technol, Sch Chem Engn, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
[3] Sinopec Shanghai Res Inst Petrochem Technol Co Ltd, State Key Lab Green Chem Engn & Ind Catalysis, Shanghai 201208, Peoples R China
基金
中国国家自然科学基金;
关键词
Selective hydrogenation; Hollow zeolites; Ni-nanoparticles; Metal encapsulation mechanism; Deactivation; LIQUID-PHASE HYDROGENATION; SELECTIVE HYDROGENATION; RU CATALYSTS; ZEOLITES; ACID; DEACTIVATION; ADSORPTION; DIFFUSION; MECHANISM; PYRIDINE;
D O I
10.1016/j.ces.2024.120913
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Anchoring active metal particles in zeolite cages can significantly improve catalytic stability. In this study, hollow silicalite-1 (HoS-1) encapsulated Ni nanoparticles catalyst (Ni@HoS-1) was prepared using the impregnation method and applied in MA hydrogenation. The encapsulation mechanism was explained as the zeolite wall restricting the evaporation of water in HoS-1, hence Ni particles would be spontaneously enriched within the zeolite cage after drying and calcination. Experiments revealed the specially designed structure effectively protected Ni particles from leaching, and after 5 cycles in liquid-phase batch reactions, the final MA conversion of Ni@HoS-1 is 40.8 % higher than that of Ni/S-1 (85.5 % vs 44.7 %). Moreover, the low acidity of Ni@HoS-1 also delayed the accumulation of carbon deposits, extending the continuous reaction lifespan from 128 h of Ni/S1 to 188 h. These findings provided a new perspective for the controllable locating of active metal sites against the supports.
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页数:14
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