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Hydrodeoxygenation of lignin-derived phenoic compounds to hydrocarbon fuel over supported Ni-based catalysts

机译:负载型镍基催化剂上木质素衍生的酚类化合物加氢脱氧为烃类燃料

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摘要

Ni-based catalysts supported on γ-Al2O3and SiO2were prepared by impregnation. Catalyst characterization was performed using XRD, NH3-TPD, H2-TPR and chemisorption. Effects of supports on catalytic performance were tested using the hydrodeoxygenation (HDO) of phenolic compounds asa model reaction. Experiment result shows that single phenolic compounds can be converted via HDO reaction over Ni/SiO2and Ni/γ-Al2O3catalysts at 300°C. The hydrocarbon yields are in the range of 60–90%. The effect of supports on the reaction mechanism was also explored. It is found that hydrogenation of the aromatic ring preferentially occurs over Ni/SiO2catalyst while the cleavage of CARO bond preferentially occurs over Ni/γ-Al2O3catalyst in the HDO of phenol. Compared to Ni/γ-Al2O3catalyst, Ni/SiO2catalyst exhibits better repeatability and higher catalytic activity for hydrocarbon yield when mixed phenolic compounds were used as feedstock in the HDO reaction, and the carbon deposited on the surface of Ni/SiO2catalyst is lower.
机译:通过浸渍法制备了负载在γ-Al2O3和SiO2上的Ni基催化剂。使用XRD,NH3-TPD,H2-TPR和化学吸附进行催化剂表征。使用酚类化合物的加氢脱氧(HDO)作为模型反应,测试了载体对催化性能的影响。实验结果表明,在300℃下,Ni / SiO2和Ni /γ-Al2O3催化剂可以通过HDO反应转化为单酚类化合物。碳氢化合物的产率在60-90%的范围内。还探讨了载体对反应机理的影响。发现在苯酚的HDO中,芳环的氢化优先于Ni / SiO2催化剂,而CARO键的裂解优先于Ni /γ-Al2O3催化剂。与混合的酚类化合物在HDO反应中用作原料相比,与Ni /γ-Al2O3催化剂相比,Ni / SiO2催化剂具有更好的重现性和更高的催化烃产率的催化活性,且Ni / SiO2催化剂表面沉积的碳较低。

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