Hydrodeoxygenation of isoeugenol over Ni-SBA-15: Kinetics and modelling

化学 加氢脱氧 异丁醇 催化作用 红外光谱学 傅里叶变换红外光谱 无机化学 活化能 核化学 物理化学 分析化学(期刊) 有机化学 化学工程 工程类 选择性 丁香酚
作者
Sebastiano Tieuli,Päivi Mäki‐Arvela,Markus Peurla,Kari Eränen,Johan Wärnå,Giuseppe Cruciani,Federica Menegazzo,Dmitry Yu. Murzin,Michela Signoretto
出处
期刊:Applied Catalysis A-general [Elsevier BV]
卷期号:580: 1-10 被引量:39
标识
DOI:10.1016/j.apcata.2019.04.028
摘要

Hydrodeoxygenation (HDO) of isoeugenol has been investigated over Ni-SBA-15 and Ni-SZ-SBA-15 containing sulfated ZrO2 with Si/Zr molar ratio of 8.4. The catalysts were prepared via incipient wetness method and characterized by N2 adsorption, AAS, TPR, X-ray diffraction (XRD), thermal gravimetric/differential thermal analyses (TG-DTA), organic elemental analysis, pyridine adsorption-desorption with Fourier-transform infrared spectroscopy (FTIR) and transmission electron microscopy (TEM). The results revealed that 75% yield of propylcyclohexane was obtained over a non acidic Ni-SBA-15 in isoeugenol HDO at 300 °C under 3 MPa H2 using dodecane as a solvent. Ni-SZ-SBA-15 gave only very low HDO activity, which is explained by location of the acid sites both inside and outside SBA-15, whereas nickel particles were partially located inside the SBA-15 structure. On the other hand Ni particles in Ni-SBA-15 with the size of 20 nm were located outside SBA-15 promoting HDO. The kinetic model was developed for HDO of isoeugenol based on the proposed reaction network, which took into account formation of intermediate products as well as oligomers. The developed kinetic model was capable of describing well the experimental data with the degree of explanation equal to 91%. The activation energy for hydrogenation of propylcyclohexene and for demethoxylation of dihydroeugenol to 4-propylphenol are equal to 92 kJ/mol and 62 kJ/mol, respectively.
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