Upgrading bio-butanol in the presence of copper-hydrotalcite derived mixed oxides: From batch to continuous flow catalytic process highly selective to butyl butyrate

被引:3
|
作者
Galletti, Anna Maria Raspolli [1 ]
Antonetti, Claudia [1 ]
Fulignati, Sara [1 ]
Licursi, Domenico [1 ]
Dell'Omo, Stefano [1 ]
Benito, Patricia [2 ]
Wilbers, Erwin [3 ]
Heeres, Hero Jan [3 ]
机构
[1] Univ Pisa, Dept Chem & Ind Chem, Via G Moruzzi 13, I-56124 Pisa, Italy
[2] Univ Bologna, Dept Ind Chem Toso Montanari, Viale Risorgimento 4, I-40136 Bologna, Italy
[3] Univ Groningen, ENTEG, Green Chem React Engn, Nijenborgh 4, NL-9747 AG Groningen, Netherlands
关键词
Copper catalysts; Hydrotalcites; Dehydrogenative coupling; Guerbet condensation; N-butanol; GUERBET CONDENSATION; N-BUTANOL; ALCOHOLS; GREEN; PRECURSORS; PROPANOL; ESTERS;
D O I
10.1016/j.cattod.2023.114288
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The conversion of bio-alcohols to chemicals and fuels can play a determinant role in the transition towards bioeconomy. Different hydrotalcite derived Cu/Mg/Al mixed oxides, having a Cu atomic content in the range 1.0-7.6 %, have been employed for the first time in batch and continuous flow reactors for the conversion of nBuOH. The catalytic performances resulted strongly tunable, being influenced by the composition of the catalytic systems and by the type of adopted reactor. The catalysts with lower Cu content resulted active both in the Guerbet condensation to 2-ethyl-1-hexanol (2EH) and in the dehydrogenative coupling (DHC) of the substrate to butyl butyrate (BB) ester, while the catalyst with the highest Cu content showed very high selectivity towards BB formation. The batch reaction evidenced a progressive deactivation of the catalytic systems with the reconstruction of the hydrotalcite precursor. On the other hand, the study in flow reactor revealed good activity and excellent stability of the catalytic system Cu7.6, a selectivity to BB > 98 mol% being maintained after 216 h of time-on-stream.
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页数:9
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