Pt-Fe-Al Trimetallic Nanoporous Catalyst for Selective Hydrogenation of α,β-Unsaturated Aldehydes

被引:0
|
作者
Wang, Yunpeng [1 ]
Wang, Shize [1 ]
Xu, Qiang [1 ,2 ]
Feng, Xiujuan [1 ]
Liu, Wei [1 ,3 ]
Yamamoto, Yoshinori [4 ]
Shi, Yantao [1 ,3 ]
Bao, Ming [1 ]
机构
[1] Dalian Univ Technol, Frontier Sci Ctr Smart Mat, State Key Lab Fine Chem, Dalian 116024, Peoples R China
[2] Dalian Univ Technol, Instrumental Anal Ctr, Dalian 116024, Peoples R China
[3] Dalian Univ Technol, Sch Chem, Dalian 116024, Peoples R China
[4] Tohoku Univ, Grad Sch Sci, Dept Chem, Sendai 9808578, Japan
基金
中国国家自然科学基金;
关键词
selective hydrogenation; PtFeAlNPore; dealloyingmethod; nanoporous; alpha; beta-unsaturatedaldehyde; allyl alcohol; CHEMOSELECTIVE REDUCTION; PREFERENTIAL OXIDATION; FORMIC-ACID; CINNAMALDEHYDE; PLATINUM; CO; PERFORMANCE; PALLADIUM; ALCOHOL; SUPPORT;
D O I
10.1021/acsanm.4c01266
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The selective hydrogenation of alpha,beta-unsaturated aldehydes using unsupported nanoporous platinum-iron-aluminum (PtFeAlNPore) as a heterogeneous catalyst was investigated in depth. A PtFeAlNPore trimetallic catalyst with a highly bicontinuous nanostructure was synthesized by a two-step chemical dealloying method. The catalyst exhibited a good yield with high selectivity for the hydrogenation of alpha,beta-unsaturated aldehydes into allyl alcohols under mild reaction conditions. A series of characterizations revealed that a decrease in the Pt electronic density (exhibiting superior hydrogen-activation ability), a nanoporous structure (providing increased reaction active sites), Lewis acidity (promoting the adsorption and activation of the carbonyl group in alpha,beta-unsaturated aldehydes), and intimate PtFe-Fe3O4 heterointerfaces (facilitating the selective hydrogenation of alpha,beta-unsaturated aldehydes into allyl alcohols) led to the excellent catalytic performance.
引用
收藏
页码:10739 / 10747
页数:9
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