Effect of Alkali Metal Addition to a Ru/CeO2 Catalyst Prepared by NaBH4 Reduction on the Catalytic Performance for H2 Production via NH3 Decomposition

被引:4
|
作者
Furusawa, Takeshi [1 ,2 ]
Sugiyama, Keita [1 ]
Kuribara, Hiroki [1 ]
Sato, Masahide [1 ,2 ]
Suzuki, Noboru [1 ,2 ]
Sato, Takafumi [1 ,2 ]
Itoh, Naotsugu [1 ]
机构
[1] Utsunomiya Univ, Grad Sch Engn, Dept Mat & Environm Chem, 7-1-2 Yoto, Utsunomiya, Tochigi 3218585, Japan
[2] Utsunomiya Univ, Grad Sch Reg Dev & Creat, Div Engn & Agr, Grad Program Mat & Environm Chem, 7-1-2 Yoto, Utsunomiya, Tochigi 3218585, Japan
关键词
H-2; Production; NH3; Decomposition; Ru/CeO2; Catalyst; Deactivation; Cs Addition; ON-SITE GENERATION; AMMONIA DECOMPOSITION; HYDROGEN-PRODUCTION; RUTHENIUM CATALYSTS; CITRIC-ACID; RU; PROMOTER; NANOPARTICLES; SUPPORT; CARRIER;
D O I
10.1252/jcej.20we130
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The Ru/CeO2 (JRC-CEO-3) catalyst prepared by NaBH4 reduction showed a high activity for NH3 decomposition compared with the other catalysts prepared in this work; however, this catalyst gradually lost its activity due to the accumulation of adsorbed species produced during the reaction. Cs significantly improved the catalytic performance of the Ru/CeO2 catalyst, and the optimum Cs/Ru molar ratio was 0.4 because excess Cs species gradually covered the exposed Ru metal active sites. Cs-Ru/CeO2-0.4 catalyzed the NH3 decomposition reaction without H-2 pretreatment because the catalyst was activated by NH3 or H-2 produced by NH3 decomposition. Moreover, Cs not only increased the N-H bond dissociation rate but also decreased the effect of the H-2 partial pressure on the catalytic performance. Consequently, the Cs-Ru/CeO2-0.4 catalyst exhibited a high, stable activity (NH3 conversion: 92% at 623 K and 60% at 573 K) with a gas hourly space velocity of 2000 mL-NH3 g-cat(-1) h(-1).
引用
收藏
页码:77 / 86
页数:10
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