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Direct synthesis of 2-ethylhexanol via n-butanal aldol condensation-hydrogenation reaction integration over a Ni/Ce-Al2O3 bifunctional catalyst

机译:在Ni / Ce-Al2O3双功能催化剂上通过正丁醛醛缩合加氢反应一体化直接合成2-乙基己醇

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摘要

Direct synthesis of 2-ethylhexanol from n-butanal via the reaction integration of n-butanal self-condensation with 2-ethyl-2-hexenal hydrogenation is of crucial interest for industrial production of 2-ethylhexanol. Furthermore, as an important and versatile chemical, n-butanol can be produced simultaneously by reaction integration. In the present work, several bifunctional catalysts based on gamma-Al2O3 were prepared by the impregnation method and were characterized by means of H-2-TPR, XRD, TEM and H-2-TPD, and their catalytic performance for direct synthesis of 2-ethylhexanol from n-butanal was investigated. The results showed that Co/Al2O3 had a low activity for hydrogenation and Cu/Al2O3 had a high selectivity for the hydrogenation of the C = O group while a Ru/Al2O3 catalyst only favored the hydrogenation of n-butanal to n-butanol. Among them, the Ni/Al2O3 catalyst showed the best catalytic performance and the yield of 2-ethylhexanol was the highest (49.4%). Ce-modified Ni/Al2O3 enhanced the competitiveness of aldol condensation versus hydrogenation of n-butanal and improved the selectivity of 2-ethylhexanol; the yield of 2-ethylhexanol rose to 57.8%. Then the influence of preparation conditions on the catalytic performance of Ni/Ce-Al2O3 was investigated and the suitable preparation conditions were obtained as follows: Ni loading = 10%, calcined at 550 degrees C for 5 h, and reduced at 570 degrees C for 4 h. The effect of reaction conditions on the integration reaction catalyzed by Ni/Ce-Al2O3 was investigated and the suitable reaction conditions were obtained as follows: weight percentage of Ni/Ce-Al2O3 = 15%, reaction temperature = 170 degrees C, reaction pressure = 4.0 MPa and reaction time = 8 h. Under the above reaction conditions, the yield of 2-ethylhexanol attained 66.9% and that of n-butanol was 18.9%. In addition, the components existing in the integration reaction system were identified by GC-MS analysis, and the main by-products were n-butyl butyrate, 2-ethylhexyl butyrate, n-butyric acid, etc. Based on the analysis of the reaction system, a reaction network for the direct synthesis of 2-ethylhexanol from n-butanal was proposed. Finally, an evaluation of the reusability of Ni/Ce-Al2O3 showed that the recovered Ni/Ce-Al2O3 catalyst lost its catalytic activity for the hydrogenation of the C = O group. The main reason for deactivation was that Ni species were covered by the flaky boehmite gamma-AlO(OH) formed from the hydration of gamma-Al2O3 in the reaction process.
机译:通过正丁醛自缩合与2-乙基-2-己烯氢化的反应整合,由正丁醛直接合成2-乙基己醇,对于工业生产2-乙基己醇至关重要。此外,作为重要且通用的化学品,可通过反应整合同时生产正丁醇。在本工作中,通过浸渍法制备了几种基于γ-Al2O3的双功能催化剂,并通过H-2-TPR,XRD,TEM和H-2-TPD对其进行了表征,以及它们对2的直接合成的催化性能。研究了来自正丁醛的-乙基己醇。结果表明,Co / Al2O3的加氢活性低,而Cu / Al2O3的C = O基团的氢化选择性高,而Ru / Al2O3催化剂仅促进正丁醛氢化为正丁醇。其中,Ni / Al2O3催化剂表现出最好的催化性能,2-乙基己醇的收率最高(49.4%)。 Ce修饰的Ni / Al2O3增强了醛醇缩合与正丁醛加氢相比的竞争力,并提高了2-乙基己醇的选择性。 2-乙基己醇的产率提高到57.8%。然后研究了制备条件对Ni / Ce-Al2O3催化性能的影响,得到了合适的制备条件:Ni的添加量= 10%,在550℃下煅烧5h,在570℃下还原。 4小时研究了反应条件对Ni / Ce-Al2O3催化的积分反应的影响,得到了合适的反应条件:Ni / Ce-Al2O3的重量百分比= 15%,反应温度= 170℃,反应压力= 4.0 MPa,反应时间= 8小时。在上述反应条件下,2-乙基己醇的产率为66.9%,正丁醇的产率为18.9%。另外,通过GC-MS分析鉴定了整合反应系统中存在的组分,主要副产物为丁酸正丁酯,丁酸2-乙基己酯,正丁酸等。提出了一种由正丁醛直接合成2-乙基己醇的反应网络。最后,对Ni / Ce-Al2O3的可重复使用性进行的评估表明,回收的Ni / Ce-Al2O3催化剂失去了其对C = O基团氢化的催化活性。失活的主要原因是,在反应过程中由水合γ-Al2O3形成的片状勃姆石γ-AlO(OH)覆盖了Ni物种。

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