Efficient hydrogenation of biomass-derived furfural to tetrahydrofurfuryl alcohol over a non-noble Ni/CeO2 catalyst under mild conditions

IF 4.9 2区 化学 Q2 CHEMISTRY, PHYSICAL
Qing Tang, Xiaoao Sun , Zidie Duan, Zisheng Xiao, Xianxiang Liu
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Abstract

Tetrahydrofurfuryl alcohol (THFA) is an important green solvent and a key feedstock for the synthesis of chemicals such as succinic acid, 1,5-pentanediol, tetrahydrofuran, and pyran. In this study, a Ni/CeO₂ catalyst was synthesized via a simple co-precipitation method, which can efficiently catalyze the hydrogenation of biomass-derived furfural to THFA under mild conditions. The catalyst was characterized using XRD, XPS, H₂-TPR, H₂-TPD, and CO₂-TPD. The results indicate that hydrogen molecules adsorb and dissociate into active hydrogen species on the highly dispersed Ni0 active sites, which then rapidly migrate to the catalyst surface to attack adsorbed furfural, generating furfuryl alcohol, which is subsequently hydrogenated to THFA. Additionally, the stability and reusability of the catalyst were thoroughly investigated. The 20Ni/CeO₂ catalyst maintained good catalytic activity after five cycles of reuse. This work demonstrates the potential of non-noble metal Ni-based catalysts for efficient hydrogenation under low-temperature and low-pressure conditions, providing a new approach for the economical and efficient production of THFA.

Abstract Image

在温和条件下,非贵重Ni/CeO2催化剂上生物质衍生的糠醛高效加氢制四氢糠醇
四氢呋喃醇是一种重要的绿色溶剂,是合成琥珀酸、1,5-戊二醇、四氢呋喃、吡喃等化工原料的重要原料。本研究通过简单共沉淀法合成了一种Ni/CeO 2催化剂,该催化剂能在温和条件下高效催化生物质衍生糠醛加氢制THFA。采用XRD、XPS、H₂-TPR、H₂-TPD和CO₂-TPD对催化剂进行了表征。结果表明,氢分子在高度分散的Ni0活性位点上吸附并解离成活性氢,然后迅速迁移到催化剂表面攻击吸附的糠醛,生成糠醛醇,糠醛醇随后被氢化成THFA。此外,还对催化剂的稳定性和可重复使用性进行了深入的研究。20Ni/CeO 2催化剂在重复使用5次后仍保持良好的催化活性。本工作证明了非贵金属镍基催化剂在低温低压条件下高效加氢的潜力,为经济高效地生产四氢呋喃提供了一条新途径。
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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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