Low-temperature redox activity and alcohol ammoxidation performance on Cu- and Ru-incorporated ceria catalysts

被引:0
作者
Chen, Chaoqi [1 ]
Ikemoto, Satoru [1 ]
Yokota, Gen-ichi [1 ]
Higuchi, Kimitaka [2 ]
Muratsugu, Satoshi [1 ,3 ]
Tada, Mizuki [1 ,3 ,4 ]
机构
[1] Nagoya Univ, Grad Sch Sci, Dept Chem, Furo Cho,Chikusa Ku, Nagoya, Aichi 4648602, Japan
[2] Nagoya Univ, Inst Mat & Syst Sustainabil, Furo Cho,Chikusa Ku, Nagoya, Aichi 4648602, Japan
[3] Nagoya Univ, Integrated Res Consortium Chem Sci, IRCCS, Furo Cho,Chikusa Ku, Nagoya, Aichi 4648602, Japan
[4] Nagoya Univ, Res Ctr Mat Sci RCMS, Furo Cho,Chikusa Ku, Nagoya, Aichi 4648602, Japan
基金
日本学术振兴会; 日本科学技术振兴机构;
关键词
NITRILES; OXIDATION; COMPLEXES; ALDEHYDES; DRIVEN;
D O I
10.1039/d4cp01432d
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
Transition-metal-incorporated cerium oxides with Cu and a small amount of Ru (Cu0.18Ru0.05CeOz) were prepared, and their low-temperature redox performance (<423 K) and catalytic alcohol ammoxidation performance were investigated. Temperature-programmed reduction/oxidation under H-2/O-2 and in situ X-ray absorption fine structure revealed the reversible redox behavior of the three metals, Cu, Ru, and Ce, in the low-temperature redox processes. The initially reduced Ru species decreased the reduction temperature of Cu oxides and promoted the activation of Ce species. Cu0.18Ru0.05CeOz selectively catalyzed the production of benzonitrile in the ammoxidation of benzyl alcohol. H-2-treated Cu0.18Ru0.05CeOz showed a slightly larger initial conversion of benzyl alcohol than O-2-treated Cu0.18Ru0.05CeOz, suggesting that the reduced structure of Cu0.18Ru0.05CeOz was active for the ammoxidation. The integration of both Cu and Ru resulted in the efficient promotion of ammoxidation, in which the Ru species were involved in the conversion of benzyl alcohol and Cu species were required for selective production of benzonitrile.
引用
收藏
页码:17979 / 17990
页数:13
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