Mixed oxides supported low-nickel formulations for the direct amination of aliphatic alcohols with ammonia

被引:47
作者
Tomer, A. [1 ,2 ]
Yan, Z. [2 ]
Ponchel, A. [1 ]
Pera-Titus, M. [2 ]
机构
[1] Univ Lille, Univ Artois, CNRS, Cent Lille,UMR 8181,UCCS, F-62300 Lens, France
[2] UMI 3464 CNRS Solvay, E2P2L, 3966 Jin Du Rd, Shanghai 201108, Peoples R China
关键词
n-Octanol; Ammonia; Direct amination; CeO2-Al2O3; Nickel; BORROWING HYDROGEN METHODOLOGY; SOLUTION COMBUSTION METHOD; CATALYTIC-ACTIVITY; X-RAY; ALUMINA CATALYSTS; TRANSITION-METAL; CARBON-DIOXIDE; STRUCTURAL-CHARACTERIZATION; NI/CEO2-AL2O3; CATALYSTS; NI CATALYSTS;
D O I
10.1016/j.jcat.2017.08.015
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
The present study focuses on the selective synthesis of primary amines from aliphatic alcohols and ammonia using alumina-ceria supported nickel formulations based on very low nickel loading (<= 2 wt%) and without any additive or external H-2 supply. The effect of the catalyst preparation methods and modes of nickel impregnation were studied in detail and comprehensively characterized. The best formulation afforded 80% n-octanol conversion with 78% selectivity to n-octylamine at optimized reaction conditions, which were far better than control catalysts and benchmark Ni-alumina formulations relying on high Ni loadings. The enhanced activities of the alumina-ceria supported nickel catalysts was attributed to three combined effects: (1) a higher reducibility of surface nickel oxide species, (2) the genesis of very small and homogeneously distributed nickel nanoparticles (2-3 nm), and (3) a strong decline in the formation of nickel aluminates. Furthermore, unlike benchmark Ni catalysts, these formulations afforded a higher resistance to leaching. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:133 / 146
页数:14
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