Department of Chemistry, School of physic and chemistry, Alzahra University, PO Box 1993891176, Vanak, Tehran, Iran.
Gas Conversion Department, Faculty of Petrochemicals, Iran Polymer and Petrochemical Institute, PO Box 14975-112, Tehran, Iran.
Int J Biol Macromol. 2024 Apr;264(Pt 1):130555. doi: 10.1016/j.ijbiomac.2024.130555. Epub 2024 Feb 29.
A novel bio-based catalyst was developed by in-situ forming Chromium(III) (Cr)-based metal-organic framework, MIL-101(Cr), in the presence of k-carrageenan (k-Car) and followed by a post-synthetic modification to introduce additional -SOH functional groups into the composite structure of k-Car/MIL-101(Cr). Different analyses were conducted to confirm the successful catalyst formation. The catalyst performance was evaluated in the solid acid catalyzed dehydration of fructose to 5-hydroxymethylfurfural. The Response Surface Method (RSM) optimization determined that employing 33 wt% of the catalyst at 105 °C for 40 min resulted in a remarkable 97.8 % yield. The catalyst demonstrated suitable recyclability, maintaining its catalytic efficiency over four cycles. Comparative studies with k-Car and the non-sulfonated composite highlighted the superior activity of the catalyst, emphasizing the synergy between the k-Car, MIL-101(Cr) and the influence of -SOH post-functionalizing on the catalytic performance.
开发了一种新型的生物基催化剂,即在存在角叉菜胶(k-Car)的情况下原位形成三价铬(Cr)基金属有机骨架 MIL-101(Cr),然后进行后合成修饰,将额外的-SOH 官能团引入 k-Car/MIL-101(Cr)的复合结构中。进行了不同的分析以确认成功制备了催化剂。在固体酸催化果糖脱水制备 5-羟甲基糠醛的反应中评估了催化剂的性能。响应面法(RSM)优化确定,在 105°C 下使用 33wt%的催化剂 40 分钟,可得到显著的 97.8%收率。该催化剂表现出良好的可重复使用性,在四个循环中保持了其催化效率。与 k-Car 和非磺化复合材料的比较研究强调了催化剂的优异活性,突出了 k-Car、MIL-101(Cr)之间的协同作用以及-SOH 后功能化对催化性能的影响。