Oxidation of 1,3-butadiene over Pd/C and Pd-Te/C catalysts in polar media

被引:1
|
作者
Trebushat, D. V. [1 ]
Kuznetsova, N. I. [1 ]
Koshcheev, S. V. [1 ]
Kuznetsova, L. I. [1 ]
机构
[1] Russian Acad Sci, Siberian Branch, Boreskov Inst Catalysis, Novosibirsk 630090, Russia
关键词
LIQUID-PHASE DIACETOXYLATION; SELECTIVE OXIDATION; MOLECULAR-OXYGEN; SODIUM LACTATE; AQUEOUS-PHASE; C CATALYST; BUTADIENE; DEACTIVATION; PYRUVATE; GLUCOSE;
D O I
10.1134/S0023158413020158
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 oxidation of 1,3-butadiene over the Pd/C and Pd-Te/C heterogeneous catalysts occurs in organic solvents containing water at a temperature of 100A degrees C and an oxygen partial pressure of atm. Crotonaldehyde dominates among the three major products of oxidation over the Pd catalyst. The introduction of Te into the catalyst increases the methyl vinyl ketone yield, the furan yield being the lowest in all cases. X-ray photoelectron spectroscopy (XPS) showed that the active catalyst components can be in a partially oxidized state, particularly after storing the catalysts in air. Additional hydrogen treatment results in almost complete reduction of the active components to metals and enhances the catalytic activity. It is supposed that the oxidation of 1,3-butadiene over the Pd-Te catalysts proceeds via the activation of dioxygen over the Pd-0 sites, with oxidized Pd and Te participating in subsequent chemical transformations.
引用
收藏
页码:233 / 242
页数:10
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