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NiAlCe mixed oxides obtained from layered double hydroxides applied to anisole hydrodeoxygenation

加氢脱氧 层状双氢氧化物 化学 催化作用 混合氧化物 无机化学 茴香醚 除氧 化学工程 有机化学 选择性 工程类
作者
Luanda Alves do Nascimento,Isabel Barroso‐Martín,Sara Raysa Silva Peçanha,Santiago Arias,Beate S. Santos,José Geraldo A. Pacheco,Antonia Infantes‐Molina,Enrique Rodrı́guez-Castellón,Ivoneide de Carvalho Lopes Barros
出处
期刊:Catalysis Today [Elsevier BV]
卷期号:394-396: 282-294 被引量:23
标识
DOI:10.1016/j.cattod.2021.08.026
摘要

Bio-oil derived from the pyrolysis of lignocellulosic biomass residues cannot be used directly as biofuel due to the high content of oxygenated compounds. As an alternative, bio-oil must undergo a deoxygenation process, such as catalytic hydrodeoxygenation (HDO). In this sense, this work studied the effect of different concentrations of Ce3+ and Ce4+ in layered double hydroxides (LDHs) in order to obtain mixed oxide catalysts containing NiAlCe (NiO-NiAl2O4-CeO2) with low cost and high performance for the hydrodeoxygenation of anisole as a model bio-oil compound. Mixed oxides were obtained from the thermal decomposition of layered double hydroxides (LDHs) by using terephthalic acid as compensation anion, with molar ratio: Ni2+/(Al3++ M) = 1.0, where M = Ce3+; Ce4+ or Ce3+-Ce4+; and Al/Ce ratios of 9 and 1. Characterization analyses confirmed the formation of LDHs for all materials, although at lower Al/Ce ratio it is observed a loss of crystallinity, due to a greater repulsion and distortion of the layer structure caused by the incorporation, in greater amount, of cations with a high ionic radius. The increase in the content of cerium in mixed oxides also led to an increase in the acidity of the catalysts, in addition to a reduction in the surface area, justified by the pore blockage by CeO2 on the catalyst surface. The greater structural and thermal stability was evidenced in the LDHs derived from Ce4+, as well as a greater dispersion of the NiO phase in the corresponding mixed oxides, and therefore presenting greater anisole conversion. The obtained data indicated that the presence of Ce4+ ions on the catalyst surface was decisive in the conversion of anisole to cyclohexane, the main deoxygenated product, obtained via the direct deoxygenation and hydrogenation mechanism.
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