Autor: |
King, Gavin M., Iqbal, Sarwat, Miedziak, Peter J., Brett, Gemma L., Kondrat, Simon A., Yeo, Benjamin R., Liu, Xi, Edwards, Jennifer K., Morgan, David J., Knight, David K., Hutchings, Graham J. |
Předmět: |
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Zdroj: |
ChemCatChem; 7/13/2015, Vol. 7 Issue 14, p2122-2129, 8p |
Abstrakt: |
The selective hydrogenation of furfuryl alcohol was investigated at room temperature by using supported palladium catalysts. The catalysts are very selective to the formation of 2-methylfuran. Furthermore, the addition of tin to palladium showed similar catalytic activity, but was more selective to tetrahydrofurfuryl alcohol. Variation of the Sn/Pd ratio has shown a considerable and interesting effect on the selectivity pattern. Addition of a small amount of Sn (1 wt %) shifted the selectivity towards tetrahydrofurfuryl alcohol and methyltetrahydrofuran, which are ring-saturated molecules. Increasing the tin ratio further decreased the catalytic activity and also showed very poor selectivity to either of these products. [ABSTRACT FROM AUTHOR] |
Databáze: |
Complementary Index |
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