Enhanced performances of bimetallic Ga-Pt nanoclusters confined within silicalite-1 zeolite in propane dehydrogenation

被引:54
作者
Wang, Yansu [1 ]
Suo, Yujun [1 ]
Lv, Xianwei [1 ]
Wang, Zheng [2 ]
Yuan, Zhong-Yong [1 ]
机构
[1] Nankai Univ, Sch Mat Sci & Engn, Minist Educ, Key Lab Adv Energy Mat Chem, Tianjin 300350, Peoples R China
[2] Ningxia Univ, State Key Lab High Efficiency Utilizat Coal & Gre, Yinchuan 750021, Ningxia, Peoples R China
基金
中国国家自然科学基金;
关键词
Propane dehydrogenation; Trace platinum; Confined Ga-Pt bimetallic nanoclusters; Silicalite-1; Electronic effect; Product desorption; PROPYLENE HYDROGENATION; CATALYSTS; CLUSTERS; PHASE; CO; NANOPARTICLES; SITES; ZINC;
D O I
10.1016/j.jcis.2021.02.129
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Ga-based catalysts are promising for use in propane dehydrogenation (PDH) because of the relatively superior activity, but the conventional Ga-based catalysts usually suffer from serious deactivation and unsatisfactory propene selectivity. Here, ultrafine bimetallic Ga-Pt nanocatalysts encapsulated into silicalite-1 (S-1) zeolites (GaPt@S-1) were synthesized by a facile ligand-protected direct H-2-reduction method. It is indicated that this catalyst is composed of confined ultra-small GaPt alloy nanoclusters and a part of isolated tetrahedral coordination of Ga species. The confined GaPt alloy nanoclusters are the active sites for PDH reaction, and their high electron density could boost the desorption of products, resulting in a high propene selectivity of 92.1% and propene formation rate of 20.5 mol g(-1) P-th(-1) at 600 degrees C. Moreover, no obvious deactivation was observed over GaPt@S-1 catalyst even after 24 h on stream at 600 degrees C, affording an extremely low deactivation constant of 0.0068 h(-1), which is much lower than that of the conventional Ga-based catalysts. Notably, the restriction of the zeolite can enhance the regeneration stability of the catalyst, and the catalytic activity kept unchanged after four consecutive cycles. (C) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页码:304 / 314
页数:11
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