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

被引:0
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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] Engineering Research Center of Large-Scale Reactor Engineering and Technology, Ministry of Education, East China University of Science & Technology, Shanghai,200237, China
[2] State Key Laboratory of Chemical Engineering, School of Chemical Engineering, East China University of Science and Technology, Shanghai,200237, China
[3] State Key Laboratory of Green Chemical Engineering and Industrial Catalysis, Sinopec Shanghai Research Institute of Petrochemical Technology Co., Ltd., Shanghai,201208, China
基金
中国国家自然科学基金;
关键词
Encapsulation - Hydrogenation - Nickel - Nickel deposits - Zeolites;
D O I
10.1016/j.ces.2024.120913
中图分类号
学科分类号
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/S-1 to 188 h. These findings provided a new perspective for the controllable locating of active metal sites against the supports. © 2024
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