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Continuous catalytic upgrading of ethanol to n-butanol and >C4 products over Cu/CeO2 catalysts in supercritical CO2

机译:超临界CO2中Cu / CeO2催化剂的乙醇至正丁醇中乙醇催化催化升高,> C4产物

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摘要

n-Butanol (BuOH) often has superior properties as a bio-fuel compared to ethanol (EtOH). However finding sustainable sources of BuOH is proving difficult. In this paper, direct production of BuOH from EtOH is compared over custom-synthesized six Cu catalysts, supported on different solid acids. These catalysts were tested in a continuous flow supercritical CO2 (scCO2) reactor, and were found to catalyse the dehydrogenation, aldol condensation and hydrogenation steps of the so-called Guerbet reaction converting EtOH to BuOH. BuOH yields and selectivities were significantly different over the four catalysts. Cu on high surface area CeO2 showed the best activity for BuOH formation, with yields above 30% achieved with good selectivity. In addition high pressure CO2 is shown to have a positive effect on the reaction, possibly due to the redox cycle of Ce2O3 and CeO2.
机译:与乙醇(EtOH)相比,正丁醇(BuOH)作为生物燃料通常具有优越的性能。然而,发现BuOH的可持续来源被证明是困难的。在本文中,将EtOH的直接生产BuOH与定制合成的六种Cu催化剂(负载在不同的固体酸上)进行了比较。这些催化剂在连续流动的超临界CO2(scCO2)反应器中进行了测试,并发现它们催化将EtOH转化为BuOH的所谓Guerbet反应的脱氢,醛醇缩合和氢化步骤。在这四种催化剂上,BuOH的收率和选择性明显不同。高表面积CeO2上的Cu对BuOH的形成表现出最好的活性,以良好的选择性可以达到30%以上的产率。另外,高压CO2对反应有积极影响,这可能是由于Ce2O3和CeO2的氧化还原循环所致。

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