DocumentCode
1912470
Title
Study on new method and mechanism of low-temperature methanol synthesis
Author
Wenze Li ; Baoyan Zhang ; Ruiqin Yang ; Chengxue Lu ; Ling Zeng ; Liujiu Xiao ; Ying Xie ; Peng Lu ; Chuang Xing ; Lei Shi ; Tsubaki, Noritatsu
Author_Institution
Sch. of Sci., Northeastern Univ., Shenyang, China
Volume
2
fYear
2011
fDate
20-22 May 2011
Firstpage
1404
Lastpage
1407
Abstract
The methanol could be synthesized from the CO/CO2/H2 on Cu/ZnO catalysts using alcohol solvent at 443 K and 3.0 Mpa. The activity of the catalyst with ZnO as carrier (Cu/ZnO) was the highest in all catalysts with Y2O3, La2O3, Al2O3, or MgO as carrier separately, and the 2-butanol as solvent exhibited the highest activity in this reaction. The studying results of the reaction mechanism show that at first adsorbed formate species were formed by adsorbing the CO/CO2/H2 on Cu/ZnO catalyst, and then the 2-butyl formate was formed by the reaction of adsorbed formate species with 2-butanol, at last the 2-butyl formate is reduced by hydrogen atoms on Cu to form methanol. The 2-butanol used in this reaction not only significantly decreased the reaction temperature due to its promotional action, but also was not consumed due to its regeneration by hydrogenation of the 2-butyl formate, acting like a catalytic solvent.
Keywords
adsorption; catalysis; catalysts; chemical technology; hydrogenation; organic compounds; reaction kinetics; 2-butanol; 2-butyl formate; Al2O3; CO-CO2-H2; Cu-ZnO; La2O3; MgO; Y2O3; adsorbed formate species; adsorption; alcohol solvent; catalysts; catalytic solvent; hydrogen atoms; hydrogenation; low-temperature methanol synthesis; reaction mechanism; reaction temperature; regeneration; Copper; Heating; Methanol; Solvents; Zinc oxide; 2-Butanol; CO/CO2 /H2 ; In-situ DRIFTS; Methanol;
fLanguage
English
Publisher
ieee
Conference_Titel
Materials for Renewable Energy & Environment (ICMREE), 2011 International Conference on
Conference_Location
Shanghai
Print_ISBN
978-1-61284-749-8
Type
conf
DOI
10.1109/ICMREE.2011.5930597
Filename
5930597
Link To Document