Supported catalysts based on Pd-In nanoparticles for the liquid- phase hydrogenation of terminal and internal alkynes: 2. catalytic properties

被引:18
|
作者
Markov, P. V. [1 ]
Bragina, G. O. [1 ]
Baeva, G. N. [1 ]
Mashkovskii, I. S. [1 ]
Rassolov, A. V. [1 ]
Yakushev, I. A. [2 ]
Vargaftik, M. N. [2 ]
Stakheev, A. Yu [1 ]
机构
[1] Russian Acad Sci, Zelinsky Inst Organ Chem, Moscow 119991, Russia
[2] Russian Acad Sci, Kurnakov Inst Gen & Inorgan Chem, Moscow 119991, Russia
基金
俄罗斯科学基金会; 俄罗斯基础研究基金会;
关键词
bimetallic catalysts; Pd; In; liquid-phase hydrogenation; terminal alkynes; internal alkynes; diphenylacetylene; phenylacetylene; 1-phenyl-1-propyne; kinetics; mechanism; INTERMETALLIC COMPOUNDS; SELECTIVE SEMIHYDROGENATION; PALLADIUM NANOPARTICLES; SURFACE DYNAMICS; PART I; METAL; DIPHENYLACETYLENE; PHENYLACETYLENE; STABILITY; PD2GA;
D O I
10.1134/S0023158416050141
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
Pd-In/Al2O3 and Pd-In/MgAl2O4 catalysts prepared from dinuclear Pd-In acetate complexes were studied in the hydrogenation of alkyne compounds with different structures. The Pd-In catalysts demonstrate high selectivity in the hydrogenation of internal alkynes comparable with that of the Lindlar catalyst. Similar activity/selectivity characteristics are reached at a significantly lower Pd content. For terminal alkynes, the favorable effect of Indium introduction is considerably less pronounced. An analysis of the In effect on the selectivity and the ratio between the rates of the first and second hydrogenation steps suggests that the reaction selectivity is determined to a large extent by a thermodynamic factor (adsorption-desorption equilibrium between the reactants and the reaction products).
引用
收藏
页码:625 / 631
页数:7
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