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Effective transformation of cellulose to 5-hydroxymethylfurfural catalyzed by fluorine anion-containing ionic liquid modified biochar sulfonic acids in water
Authors:Chao Zhang  Zengtian Cheng  Zaihui Fu  Yachun Liu  Xianfeng Yi  Anmin Zheng  Steven Robert Kirk  Dulin Yin
Affiliation:1.National and Local United Engineering Laboratory for New Petrochemical Materials and Fine Utilization of Resources, Key Laboratory of Resource Fine-Processing and Advanced Materials of Hunan Province and Key Laboratory of Chemical Biology and Traditional Chinese Medicine Research (Ministry of Education of China), College of Chemistry and Chemical Engineering,Hunan Normal University,Changsha,China;2.Wuhan Center for Magnetic Resonance, State Key Laboratory of Magnetic Resonance and Atomic and Molecular Physics, Wuhan Institute of Physics and Mathematics,Chinese Academy of Sciences,Wuhan,China
Abstract:This article first discloses that the fluorine anion-containing ionic liquids-functionalized biochar sulfonic acids (BCSA-IL-F1–3s), which were simply synthesized by an ionic exchange of 1-trimethoxysilylpropyl-3-methylimidazolium chloride (IL-Cl) grafted on the BCSA with CF3SO3H (HF1), HBF4 (HF2), HPF6 (HF3), respectively, can efficiently catalyze cellulose hydrolysis into reducing sugars (RSs) and 5-hydroxymethyl furfural (HMF) in water under microwave irradiation. This process provides a very high catalysis efficiency (turnover numbers, 4.03–4.89) at mild temperature (80 °C) for 3 h, but also possesses an excellent repeatability. More outstandingly, they can achieve much higher HMF yields (12.70–27.94%) compared to the IL-Cl-functionalized BCSA catalyst (HMF yields are lower than 0.1%) under the same reaction conditions. This is likely because the introduction of IL-F1–3s groups can significantly improve the accessibility, acidity and thermal stability of BCSA’s SO3H sites, as supported by evidence from a solid 31P NMR spectrum and thermogravimetric analysis. It is proposed that the good selectivity for HMF perhaps originates from a co-catalysis action of the IL-F1–3s and SO3H groups on BCSA-IL-F1–3s in the further conversion of RSs to HMF.
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