Performances of mixed alcohols synthesis over potassium promoted molybdenum carbides

Molybdenum carbides, β-Mo 2C and α-MoC 1− X , promoted by K 2CO 3 were studied as catalysts for CO hydrogenation reactions at T = 573 K, P = 8.0 MPa, GHSV = 2000 h −1, H 2/CO = 1.0. Unpromoted molybdenum carbides produced mainly light hydrocarbons under these conditions. Addition of K 2CO 3 as a pro...

Full description

Saved in:
Bibliographic Details
Published inFuel (Guildford) Vol. 85; no. 17; pp. 2662 - 2665
Main Authors Xiang, Minglin, Li, Debao, Li, Wenhuai, Zhong, Bing, Sun, Yuhan
Format Journal Article
LanguageEnglish
Published Oxford Elsevier Ltd 01.12.2006
Elsevier
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Molybdenum carbides, β-Mo 2C and α-MoC 1− X , promoted by K 2CO 3 were studied as catalysts for CO hydrogenation reactions at T = 573 K, P = 8.0 MPa, GHSV = 2000 h −1, H 2/CO = 1.0. Unpromoted molybdenum carbides produced mainly light hydrocarbons under these conditions. Addition of K 2CO 3 as a promoter, however, both β-Mo 2C and α-MoC 1− X resulted in remarkable selectivity shift from hydrocarbons to alcohols. Moreover, the promoter of potassium enhanced the ability of chain propagation of β-Mo 2C and α-MoC 1− X with higher selectivity to C 2+OH. Meanwhile, the investigation of the loadings of K 2CO 3 in β-Mo 2C and α-MoC 1− X revealed that the maximum of yield of alcohol was obtained at K/Mo (molar ratio) of 0.2 and 0.1, respectively. On K/β-Mo 2C catalysts, the distribution of hydrocarbons obeyed traditional linear A–S–F plot, while alcohols gave a unique linear A–S–F distribution with remarkable deviation of methanol compared with that of on β-Mo 2C catalyst. However, there was no significant difference between α-MoC 1− X and K/α-MoC 1− X catalysts about the distributions of alcohols and hydrocarbons; they both have similar linear A–S–F plots. Thus, the potassium promoter played a different role over β-Mo 2C and α-MoC 1− X catalysts upon the catalytic performance of mixed alcohols synthesis.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0016-2361
1873-7153
DOI:10.1016/j.fuel.2006.05.012