脱氢
热液循环
催化作用
选择性
非阻塞I/O
材料科学
化学工程
乙烯
化学计量学
纹理(宇宙学)
氧气
无机化学
化学
有机化学
人工智能
工程类
图像(数学)
计算机科学
作者
Dong Li,Lian Kong,Xiaoqiang Fan,Zean Xie,Xia Xiao,Zhen Zhao
标识
DOI:10.1002/slct.202201473
摘要
Abstract The oxidative dehydrogenation of ethane (ODHE) to ethylene is a process with many advantages (such as energy conservation and coke resistance). Herein, flower‐like Ni−Al−O catalysts with hierarchical structure and high surface areas were fabricated through a hydrothermal route and were applied to ODHE using O 2 as oxidant. Compared with NiO alone, the Al 3+ insertion into NiO matrix not only increases the C 2 H 4 selectivity by 3–4 times, but also prevents the generation of CO 2 and CH 4 above 500 °C. At 550 °C, all Ni−Al−O catalysts maintain approximately 50 % ethylene selectivity regardless of Al content. The ethylene yield of 29.5 % with C 2 H 4 selectivity 55.7 % over Ni−Al 0.8 ‐O sample can be reached at 500 °C. Moreover, the Ni−Al 0.8 ‐O catalyst presents a good stability and has no loss of activity after 100 h continuous evaluation. The various characterizations were carried out for investigating the nature of as‐prepared Ni−Al−O catalysts with different Al loadings. Experimental results demonstrate that the addition of Al not only affects the structure and texture properties of NiO, but also impacts the reducibility of Ni species and the amount of active oxygen species. It is found that the Al 3+ substitution results in: (1) smaller NiO size; (2) larger specific surface area; (3) weaker reducibility and (4) fewer non‐stoichiometric oxygen species. Therefore, the significant improvement of ethylene selectivity is observed in Ni−Al x ‐O catalysts.
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