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Influence of Solvent on Liquid Phase Hydrodeoxygenation of Furfural-Acetone Condensation Adduct using Ni/Al2O3-ZrO2 Catalysts

机译:溶剂对使用Ni / Al2O3-ZrO2催化剂的糠醛 - 丙酮缩合加合物液相加氢脱氧的影响

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Influence of water and acidic protic solvent on hydrodeoxygenation (HDO) of the furfural-acetone adduct (FAA) over Ni/Al2O3-ZrO2 (NiAZ) catalysts were investigated. The HDO of FAA was carried out in a batch reactor at 150°C for 8 hours. The NiAZ catalysts were home-made catalysts which were prepared by wet impregnation method with 10 and 20% nickel loading. The HDO reaction of FAA using lONiAZ in water at 150°C gave alkane and oxygenated hydrocarbons at 31.41% with selectivity over tridecane (C13) in 6.67%. On the other hand, a reaction using acetic acid:water (1:19 v/v) in similar reaction condition gave only oxygenated compounds and hydrocracking product (C8-C10). The formation of tridecane (C13) was proposed by hydrogenation of C=O and C=C followed by decarboxylation without hydrocracking process. The presence of water facilitated decarboxylation mechanism by stabilized dehydrogenated derivatives of FAA.
机译:研究了水和酸性质粒溶剂对Ni / Al 2 O 3-ZrO2(NIAZ)催化剂的糠醛 - 丙酮加合物(FAA)的加氢脱氧(HDO)的影响。 FAA的HDO在150℃下在批量反应器中进行8小时。 NIAZ催化剂是通过湿浸渍方法制备的本土催化剂,其具有10和20%镍负载。 FAA在150℃下使用LoniAz在水中使用Loniaz的HDO反应在31.41%的31.41%下进行烷烃和含氧烃,在6.67%的6.67%中选择性葡萄烷(C13)。另一方面,使用乙酸的反应:类似反应条件的水(1:19V / V)仅含氧化合物和加氢裂化产物(C8-C10)。通过氢化C = O和C = C,提出了三癸烷(C13)的形成,然后在不加氢裂化过程的情况下进行脱羧。通过FAA的稳定脱氢衍生物存在水促进的脱羧机理。

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