TiS2催化下一锅微波辅助果糖醚化制备可持续液体燃料的研究

IF 3.9 3区 化学 Q2 CHEMISTRY, PHYSICAL
ChemCatChem Pub Date : 2025-06-28 DOI:10.1002/cctc.202500504
Nidhi Kushwaha, Ejaz Ahmad, Kamal K. Pant
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引用次数: 0

摘要

本研究合成了TiS2催化剂,在500°C、600°C、700°C和800°C条件下对其进行部分还原生成活性位点,从而增强了催化剂将果糖转化为5-乙氧基甲基糠醛(EMF)的性能。部分还原导致TiS2-x的形成,从而产生刘易斯酸中心。在反应介质中,路易斯中心与极性质子溶剂相互作用,形成H+基团,促进果糖脱水。催化剂TiS2、TiS2500、TiS2600、TiS2700和TiS2800的酸强度分别为1.08、1.44、1.69、1.27和1.36 mmol/g。对所制备的催化剂进行了连续脱水果糖和5-羟甲基糠醛(HMF)醚化反应的测试,结果表明,在160°C条件下,30分钟内的EMF产率为63%。研究结果表明,S空位与催化剂的酸度和活性之间存在一定的关系。果糖脱水和HMF醚化反应的活化能(140 ~ 160℃)分别为44.67 kJ/mol和20.86 kJ/mol,与其他Brønsted酸催化剂相当。此外,速率常数表明HMF醚化反应(k2 = 5.77 ~ 7.8 min−1)比果糖脱水反应(k1 = 2.93 ~ 5.6 min−1)更快,这表明通过整合生物可再生原料、催化剂和绿色质子溶剂,HMF醚化反应是一个理想的绿色化学过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

One-Pot Microwave Assisted Etherification of Fructose to Sustainable Liquid Fuel Over TiS2 Catalyst

One-Pot Microwave Assisted Etherification of Fructose to Sustainable Liquid Fuel Over TiS2 Catalyst

One-Pot Microwave Assisted Etherification of Fructose to Sustainable Liquid Fuel Over TiS2 Catalyst

One-Pot Microwave Assisted Etherification of Fructose to Sustainable Liquid Fuel Over TiS2 Catalyst

In this study, TiS2 catalyst was synthesized, which was partially reduced at 500 °C, 600 °C, 700 °C, and 800 °C to generate the active sites which resulted in enhanced catalysts’ performance for transforming fructose to 5-ethoxymethylfurfural (EMF). The partial reduction resulted in the formation of TiS2-x giving rise to Lewis acid centers. The Lewis centers interact with the polar protic solvent in the reaction medium, forming H+ moieties which facilitated the dehydration of fructose. The catalysts TiS2, TiS2500, TiS2600, TiS2700, and TiS2800 showed acid strengths of 1.08, 1.44, 1.69, 1.27, and 1.36 mmol/g, respectively. The prepared catalysts were tested for successive dehydration of fructose and etherification of 5-hydroxymethylfurfural (HMF) resulting in an efficient 63% EMF yield at 160 °C in 30 min. The relationship between S vacancies, acidity and activity of the catalyst is well established in the study. The activation energies (140–160 °C) for fructose dehydration and HMF etherification were 44.67 kJ/mol and 20.86 kJ/mol respectively, which were comparable to other Brønsted acid catalysts. Additionally, rate constants indicates that HMF etherification (k2 = 5.77 to 7.8 min−1) is faster than fructose dehydration (k1 = 2.93 to 5.6 min−1) reaction showcasing an ideal green chemical process by integrating bio-renewable feedstock, catalyst, and green protic solvent.

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来源期刊
ChemCatChem
ChemCatChem 化学-物理化学
CiteScore
8.10
自引率
4.40%
发文量
511
审稿时长
1.3 months
期刊介绍: With an impact factor of 4.495 (2018), ChemCatChem is one of the premier journals in the field of catalysis. The journal provides primary research papers and critical secondary information on heterogeneous, homogeneous and bio- and nanocatalysis. The journal is well placed to strengthen cross-communication within between these communities. Its authors and readers come from academia, the chemical industry, and government laboratories across the world. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies, and is supported by the German Catalysis Society.
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