Synergistic effects of Pt-embedded, MIL-53-derived catalysts (Pt@Al2O3) and NaBH4 for water-mediated hydrogenolysis of biomass-derived furfural to 1,5-pentanediol at near-ambient temperature

氢解 化学 糠醛 催化作用 硼氢化钠 呋喃 化学工程 糠醇 产量(工程) 铂金 密度泛函理论 无机化学 有机化学 计算化学 工程类 材料科学 冶金
作者
Jyun-Yi Yeh,Babasaheb M. Matsagar,Season S. Chen,Hsiang-Ling Sung,Daniel C.W. Tsang,Yi‐Pei Li,Kevin C.‐W. Wu
出处
期刊:Journal of Catalysis [Elsevier BV]
卷期号:390: 46-56 被引量:57
标识
DOI:10.1016/j.jcat.2020.07.014
摘要

We demonstrate an effective and selective conversion of biomass-derived furfural (FAL) to 1,5-pentanediol (1,5-PD) with high yields through a water-mediated hydrogenolysis process under mild reaction conditions (45 °C, aqueous media). A novel alumina-supported platinum catalyst ([email protected]2O3) with high-loading and uniform distribution of Pt nanoparticles is prepared through in situ synthesis of Pt-embedded metal–organic frameworks (i.e., MIL-53(Al)-NH2). As a typical example, a high yield of 75.2% 1,5-PD can be achieved from FAL conversion. A possible reaction mechanism is proposed based on the experimental and computational findings, including XPS analysis, kinetic studies, acidity measurements, and density functional theory (DFT) calculations. The high effectiveness of the proposed system is attributed to (1) the strong metal support interaction (SMSI) between Pt and penta-coordination aluminum, and (2) the synergistic effects of Brønsted acidic alumina support and the presence of sodium metaborate (NaBO2). Sodium borohydride (NaBH4) acts as both a hydrogen donor and a precursor for NaBO2, which results in an exclusive FAL to 1,5-PD (i.e., no 1,2-pentanediol) by regulating the water-mediated hydrogenolysis pathway as revealed by experiments and DFT calculations. The reaction strategy proposed in this study has also manifested remarkable versatility for a wide range of furan derivatives.

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