Combination and interaction of ammonia synthesis ruthenium catalysts

A novel combination-type ruthenium catalyst has been developed, in which two catalysts, K-Ru/MgO and K-Ru/CNTs, are combined with weight ratio of 1/1. The hightest activity of the combination-type catalyst, K-Ru/CNTs + K-Ru/MgO, reaches 4453   μ mol   N H 3   h − 1   g − cat − 1 at 673 K under 0.2 M...

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Published inJournal of molecular catalysis. A, Chemical Vol. 259; no. 1; pp. 218 - 222
Main Authors Xu, Qing-Chi, Lin, Jing-Dong, Li, Jun, Fu, Xian-Zhu, Yang, Zhen-Wei, Guo, Wei-Ming, Liao, Dai-Wei
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier B.V 15.11.2006
Elsevier
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Abstract A novel combination-type ruthenium catalyst has been developed, in which two catalysts, K-Ru/MgO and K-Ru/CNTs, are combined with weight ratio of 1/1. The hightest activity of the combination-type catalyst, K-Ru/CNTs + K-Ru/MgO, reaches 4453   μ mol   N H 3   h − 1   g − cat − 1 at 673 K under 0.2 MPa, which is two times higher than the average activity of the two catalysts. ▪ Based on combination advantages of both supports MgO and carbon nanotubes (CNTs), a novel combination-type catalyst for ammonia synthesis has been developed, in which two catalysts, K-Ru/MgO and K-Ru/CNTs, are combined with the optimal weight ratio of 1/1. The results show that the highest catalytic activity of the combination-type ruthenium catalyst, K-Ru/CNTs + K-Ru/MgO, for ammonia synthesis reaches 4453   μ mol   N H 3   h − 1   g − cat − 1 at 673 K under 0.2 MPa, which is about two times higher than the average activity of the two catalysts under the same operating conditions. It is suggested that there is a complementary interaction between the two supports (CISS), MgO and CNTs, and the combination of both K-MgO and K-CNTs promotes electron transfer from alkali metallic atoms to the B 5-sites of ruthenium.
AbstractList A novel combination-type ruthenium catalyst has been developed, in which two catalysts, K-Ru/MgO and K-Ru/CNTs, are combined with weight ratio of 1/1. The hightest activity of the combination-type catalyst, K-Ru/CNTs + K-Ru/MgO, reaches 4453   μ mol   N H 3   h − 1   g − cat − 1 at 673 K under 0.2 MPa, which is two times higher than the average activity of the two catalysts. ▪ Based on combination advantages of both supports MgO and carbon nanotubes (CNTs), a novel combination-type catalyst for ammonia synthesis has been developed, in which two catalysts, K-Ru/MgO and K-Ru/CNTs, are combined with the optimal weight ratio of 1/1. The results show that the highest catalytic activity of the combination-type ruthenium catalyst, K-Ru/CNTs + K-Ru/MgO, for ammonia synthesis reaches 4453   μ mol   N H 3   h − 1   g − cat − 1 at 673 K under 0.2 MPa, which is about two times higher than the average activity of the two catalysts under the same operating conditions. It is suggested that there is a complementary interaction between the two supports (CISS), MgO and CNTs, and the combination of both K-MgO and K-CNTs promotes electron transfer from alkali metallic atoms to the B 5-sites of ruthenium.
Author Li, Jun
Lin, Jing-Dong
Guo, Wei-Ming
Yang, Zhen-Wei
Liao, Dai-Wei
Xu, Qing-Chi
Fu, Xian-Zhu
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Issue 1
Keywords Support–support interaction
Carbon nanotubes
Combination-type ruthenium catalyst
Ammonia synthesis
Magnesia
Mixed catalyst
Ruthenium
Support
Transition metal
Alkali metal
Ammonia
Heterogeneous catalysis
Synthesis
Support-support interaction
Platinoid
Magnesium Oxides
Potassium
Catalyst
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Snippet A novel combination-type ruthenium catalyst has been developed, in which two catalysts, K-Ru/MgO and K-Ru/CNTs, are combined with weight ratio of 1/1. The...
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StartPage 218
SubjectTerms Ammonia synthesis
Carbon nanotubes
Catalysis
Chemistry
Combination-type ruthenium catalyst
Exact sciences and technology
General and physical chemistry
Magnesia
Support–support interaction
Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry
Title Combination and interaction of ammonia synthesis ruthenium catalysts
URI https://dx.doi.org/10.1016/j.molcata.2006.06.030
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