在 RuNi 双金属催化剂上将正己醇胺化为正己胺

IF 2.8 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Boyun Gao, Huijiang Huang, Mooeez Ur Rehman, Bin Ren, Yuruo Liu, Weipeng Fan, Pengfei Li, Lizhi Zhang, Yan Xu, Yujun Zhao
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引用次数: 0

摘要

背景通过脂肪醇胺化合成脂肪胺为环境友好型生产提供了一种前景广阔的途径,特别是与使用氢氰酸的方法相比,使用氢氰酸的方法往往涉及大量排放。结论 催化剂的表征结果表明,在双金属催化剂中,钌和镍之间存在显著的相互作用,从而提高了镍的还原性,改善了金属的分散性。此外,研究还发现钌在将 NH3 离解为 NHx(x = 1,2)的过程中发挥了重要作用,从而显著改善了正己醇在镍位点的脱氢过程。两种金属位点之间的协同效应成为促进醇胺化过程的关键因素。© 2024 化学工业学会(SCI)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Amination of n‐hexanol to n‐hexylamine over RuNi bimetallic catalyst
BACKGROUNDThe synthesis of fatty amines via fatty alcohol amination offers a promising avenue for environmentally friendly production, particularly when compared with the methods employing hydrocyanic acid which often involve significant emissions.RESULTThis study explores the synthesis of n‐hexylamine through one‐step amination of n‐hexanol utilizing a series of Ru‐doped Ni catalysts supported over γ‐Al2O3, achieving 61% n‐hexanol yield, 35% dihylamine yield and 3.5% trihylamine yield at the n‐hexanol conversion of 99%.CONCLUSIONThe characterization results of the catalysts revealed a significant interaction between ruthenium and nickel in the bimetallic catalysts, leading to the enhanced reducibility of Ni species and improved metal dispersion. Moreover, ruthenium species were found to play an important role in the dissociation of NH3 into NHx (x = 1, 2), thereby significantly improving the dehydrogenation process of n‐hexanol at Ni sites. The synergistic effect between the two kinds of metal sites emerges as crucial factor for the boosted alcohols amination process. © 2024 Society of Chemical Industry (SCI).
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来源期刊
CiteScore
7.00
自引率
5.90%
发文量
268
审稿时长
1.7 months
期刊介绍: Journal of Chemical Technology and Biotechnology(JCTB) is an international, inter-disciplinary peer-reviewed journal concerned with the application of scientific discoveries and advancements in chemical and biological technology that aim towards economically and environmentally sustainable industrial processes.
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