Hydrogenation of nitriles to primary amines on metal-supported catalysts: Highly selective conversion of butyronitrile to n-butylamine

被引:56
作者
Segobia, D. J. [1 ]
Trasarti, A. F. [1 ]
Apesteguia, C. R. [1 ]
机构
[1] UNL CONICET, INCAPE, Catalysis Sci & Engn Res Grp GICIC, RA-3000 Santa Fe, Argentina
关键词
Butyronitrile hydrogenation; Selective hydrogenation; Primary amines; Metal-supported catalysts; LIQUID-PHASE HYDROGENATION; RANEY-CO CATALYSTS; NICKEL-CATALYSTS; IN-SITU; ACETONITRILE; SPECTROSCOPY; MECHANISM; COPPER;
D O I
10.1016/j.apcata.2012.08.006
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 selective liquid-phase hydrogenation of butyronitrile to n-butylamine was studied in a batch reactor on Co(9.8%)/SiO2, Ni(10.5%)/SiO2, Cu(9.2%)/SiO2, Pt(0.27%)/SiO2, Pd(0.33%)/SiO2, and Ru(1.8%)/SiO2 catalysts. At 373 K and 13 bar (H-2), the initial butyronitrile conversion rate (r(BN)(0), mmol/hg) followed the order Ni > Co > Pt > Ru > Cu > Pd. Cu/SIO2 and Pd/SiO2 did not form n-butylamine and rapidly deactivated during the progress of the reaction. Pt/SiO2 produced mainly dibutylamine and only minor amounts of n-butylamine and tributylamine. In contrast, Ru/SiO2 formed preponderantly n-butylamine but also produced significant amounts of dibutylamine and butylidene-butylamine, an intermediate in the formation pathway of the secondary amine. The highest yield to n-butylamine was obtained on Ni/SiO2 (84%). Co/SiO2 was initially highly selective to n-butylamine but with the progress of the reaction the butylamine concentration in the reaction mixture diminished because it partially reacted with the solvent (ethanol) to form N-ethylbutylamine. In an attempt to reduce the formation of byproducts, Ni/SiO2 and Co/SiO2 catalysts were tested at lower temperatures and higher H-2 pressures. Butyronitrile was selectively converted to n-butylamine on Co/SiO2 at 343 K and 25 bar, yielding 97% of n-butylamine, similarly to the highest yields reported on Raney Co catalysts. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:69 / 75
页数:7
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