Low-temperature dehydrogenation of dodecahydro-N-ethylcarbazole catalyzed by PdCo bimetallic oxide

被引:10
|
作者
Li, Xiaoxuan [1 ,2 ]
Wu, Fei [3 ]
Zhou, Wenhua [1 ,2 ]
Chen, Chao [1 ,2 ]
Wang, Jianghao [1 ,2 ]
Li, Bolong [1 ,2 ]
Chen, Hao [4 ]
Fu, Jie [1 ,2 ]
机构
[1] Zhejiang Univ, Coll Chem & Biol Engn, Key Lab Biomass Chem Engn, Minist Educ, Hangzhou 310027, Peoples R China
[2] Inst Zhejiang Univ Quzhou, Quzhou 324000, Zhejiang, Peoples R China
[3] Wuhan Inst Marine Elect Prop, Wuhan 430064, Hubei, Peoples R China
[4] Hunan Univ, Coll Chem & Chem Engn, Changsha 410082, Hunan, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
Liquid organic hydrogen carrier; Dodecahydro-N-ethylcarbazole; Low-temperature dehydrogenation; PdCoOx; REDUCED GRAPHENE OXIDE; ORGANIC HYDROGEN CARRIER; CARBON NITRIDE; PERFORMANCE; NANOPARTICLES; STORAGE; KINETICS; RELEASE;
D O I
10.1016/j.ces.2023.118650
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Liquid organic hydrogen carriers have attracted significant attention for hydrogen storage and trans-portation and have been extensively investigated. Pd-based noble metal catalysts have been reported as some of the most active catalysts, however, achieving an optimal Pd utilization efficiency and stability remains challenging but significant. Herein, a PdCoOx-based bimetallic oxide catalyst was prepared and applied for the low-temperature dehydrogenation of dodecahydro-N-ethylcarbazole (12H-NECZ) to pro-duce H2, utilizing the following advantages: (1) the activity of Pd was enhanced by introducing Co to form a PdCoOx bimetallic oxide site; (2) the electronic state of the catalyst was tuned based on the interfacial effect between the PdCoOx and Zr-C3N4 supports. Thus, PdCo bimetallic oxide formation improved the electronic transfer rate and the interaction between the support and PdCoOx, thereby enhancing the cat-alytic dehydrogenation activity. Consequently, 12H-NECZ was completely dehydrogenated with 95.6 % selectivity at 140 degrees C for 8 h, with only 2.63 wt% Pd loading.(c) 2023 Elsevier Ltd. All rights reserved.
引用
收藏
页数:10
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