Efficient Conversion of Biomass‐Derived Furfural to Tetrahydrofurfuryl Alcohol over Co3O4−C Nanocomposite Catalyst at Mild Conditions

糠醛 催化作用 糠醇 活化能 硼氢化钠 阿累尼乌斯方程 反应速率常数 水溶液 无机化学 有机化学 核化学 化学 动力学 物理 量子力学
作者
Chi Văn Nguyên,Giau M. Le,Tung T. Nguyen,Thuan Van Tran,To Vu Thanh Dien,Phuong‐Tung Nguyen,Ngoc Quyên Trân,Nam T. S. Phan
出处
期刊:ChemistrySelect [Wiley]
卷期号:8 (5) 被引量:1
标识
DOI:10.1002/slct.202203429
摘要

Abstract Due to the depletion of fossil fuel resources, catalytic conversion of biomass into liquid fuels and valuable compounds has become an attractive field of research. Tetrahydrofurfuryl alcohol (THFAL) is an important platform molecule in both industrial and pharmacological fields, and catalytic hydrogenation of furfural (FA) to THFAL is a sustainable process. However, an active and stable catalyst for the direct hydrogenation of FA to THFAL under milder conditions is still a challenge. Accordingly, herein, we investigated a high‐valence metal catalyst (Co 3 O 4 −C) for the hydrogenation of FA to THFAL using sodium borohydride (NaBH 4 ) as the H source. Under optimal reaction conditions (that is, 0.05 g Co 3 O 4 −C‐700 in an aqueous solution, 5 mmol NaBH 4 , 60 °C, and 3 h), 88.5 % THFAL was produced over Co 3 O 4 −C‐700. The kinetic study revealed that furfuryl alcohol was generated as an intermediate during the hydrogenation of FA. Additionally, the reaction followed pseudo‐first order kinetics, and the reaction rate constant (k) values were .80, 3.41, 3.45, and 5.55 h −1 at 30, 40, 45, 50, and 60 °C, respectively. From the slopes of the Arrhenius plot, the activation energy was determined to be 22.02 kJ mol −1 , indicating high activity of the catalyst for the reaction. Moreover, Co 3+ and smaller sizes of Co 3 O 4 nanoparticles contributed to the activity of Co 3 O 4 −C‐700. We believe that the metal oxide catalyst developed herein can be used for various biomass conversions.

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