Mg/Al and Cu-Mg/Al mixed oxides derived from hydrotalcites as catalysts to produce 1-butanol from ethanol

IF 4.9 2区 化学 Q2 CHEMISTRY, PHYSICAL Molecular Catalysis Pub Date : 2024-09-16 DOI:10.1016/j.mcat.2024.114528
Julieta A. Rubio-Rueda , Juan P. Quevedo-Hernandez , Mónica B. López , Johan Fabian Galindo , Gina Hincapié-Triviño
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Abstract

The interaction between ethanol molecules to produce 1-butanol over surfaces of Mg/Al and Cu-Mg/Al oxides derived from hydrotalcites (HT) was studied experimentally and computationally. For Mg/Al catalyst, the insertion of Al in the MgO lattice generates a selectivity of 11.7 % for 1-butanol and of 5.8 % for diethyl ether at 300 °C, indicating the importance of the presence of acid sites for dehydration. For Cu-Mg/Al catalyst, Cu2+ cations have been structural substituted, instead of superficial substituted, exhibiting the highest selectivity for 1-butanol at 250 °C (16.5 %). The inclusion of copper increases the number of acid-base pairs, which are important in the dehydrogenation of ethanol molecules, the aldol condensation of acetaldehyde molecules and the subsequent steps to get 1-butanol. According to DFT results, the presence of copper favors the adsorption of ethanol on the surface, weakening the Cα-Hα bond of the molecule, contributing to the formation of acetaldehyde.

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以氢化铝酸盐衍生的镁/铝和铜-镁/铝混合氧化物为催化剂,从乙醇生产 1-丁醇
我们通过实验和计算研究了乙醇分子在氢铝酸盐(HT)衍生的 Mg/Al 和 Cu-Mg/Al 氧化物表面上生成 1-丁醇的相互作用。对于镁/铝催化剂,在 300 °C 时,铝插入氧化镁晶格可产生 11.7 % 的 1-丁醇选择性和 5.8 % 的二乙醚选择性,这表明酸性位点的存在对脱水的重要性。在 Cu-Mg/Al 催化剂中,Cu2+ 阳离子被结构取代,而不是表面取代,在 250 °C 时对 1-丁醇的选择性最高(16.5%)。铜的加入增加了酸碱对的数量,而酸碱对在乙醇分子的脱氢、乙醛分子的醛缩合以及随后得到 1-丁醇的步骤中非常重要。根据 DFT 结果,铜的存在有利于乙醇在表面的吸附,削弱了乙醇分子的 Cα-Hα 键,从而促进了乙醛的形成。
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来源期刊
Molecular Catalysis
Molecular Catalysis Chemical Engineering-Process Chemistry and Technology
CiteScore
6.90
自引率
10.90%
发文量
700
审稿时长
40 days
期刊介绍: Molecular Catalysis publishes full papers that are original, rigorous, and scholarly contributions examining the molecular and atomic aspects of catalytic activation and reaction mechanisms. The fields covered are: Heterogeneous catalysis including immobilized molecular catalysts Homogeneous catalysis including organocatalysis, organometallic catalysis and biocatalysis Photo- and electrochemistry Theoretical aspects of catalysis analyzed by computational methods
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