Silver modified Cu/SiO2 catalyst for the hydrogenation of methyl acetate to ethanol
Catalysis, Kinetics and Reaction Engineering|Updated:2026-01-06
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Silver modified Cu/SiO2 catalyst for the hydrogenation of methyl acetate to ethanol
Chinese Journal of Chemical EngineeringIssue 6, Pages: 1612-1622(2020)
Affiliations:
1. Chengdu Institute of Organic Chemistry, Chinese Academy of Sciences,Chengdu,China,610041
2. National Engineering Laboratory for VOCs Pollution Control Material & Technology, University of Chinese Academy of Sciences,Beijing,China,101408
3. CAS Key Laboratory of Green Process and Engineering, State Key Laboratory of Multiphase Complex Systems, The National Key Laboratory of Clean and Efficient Coking Technology, Beijing Key Laboratory of Ionic Liquids Clean Process, Institute of Process Engineering, Chinese Academy of Sciences,Beijing,China,100190
4. Zhongke Langfang Institute of Process Engineering,Zhengzhou,China,450000
5. School of Chemical Science, University of Chinese Academy of Sciences,Beijing,China,100049
Zhiheng Ren, Muhammad Naeem Younis, Hui Zhao, et al. Silver modified Cu/SiO2 catalyst for the hydrogenation of methyl acetate to ethanol[J]. Chinese Journal of Chemical Engineering, 2020, (6): 1612-1622. DOI: 10.1016/j.cjche.2020.02.011.
DOI:
Zhiheng Ren, Muhammad Naeem Younis, Hui Zhao, et al. Silver modified Cu/SiO2 catalyst for the hydrogenation of methyl acetate to ethanol[J]. Chinese Journal of Chemical Engineering, 2020, (6): 1612-1622. DOI: 10.1016/j.cjche.2020.02.011.DOI:
Silver modified Cu/SiO2 catalyst for the hydrogenation of methyl acetate to ethanol
catalysts were synthesized with ammonia-evaporation method and applied in vapor-phase hydrogenation of methyl acetate to ethanol. The influence of additive ‘Ag’ on the structural evolution of catalyst was systematically studied by several characterization techniques
such as N
2
adsorption-desorption
N
2
O titration
PXRD
FTIR
in-situ
FTIR
H
2
-TPR
H
2
-TPD
XPS and TEM. Results showed that incorporation of a small amount of Ag could enhance the structural stability
and the strong interaction between Cu and Ag species was conducive to increase the dispersion of copper species and create a suitable Cu
+
/(Cu
0
+ Cu
+
) ratio
which was proposed to be responsible for the improved catalytic activity. The maximum conversion of MA (94.1%) and selectivity of ethanol (91.3%) over optimized Cu-0.5Ag/SiO
2
and 120 h on stream without deactivation under optimal conditions demonstrates its excellent stability.
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