合成 UiO-66-SO3H-Cl 作为可回收的多功能催化剂,用于将葡萄糖高效转化为 5-羟甲基糠醛

IF 1.7 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY
Molood Falsafin, Kamal Ghani, Arash Shokrollahi
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引用次数: 0

摘要

摘要 5-羟甲基糠醛(HMF)是将生物质转化为多种生物质衍生化学品和生物燃料的主要平台组合,一直受到广泛关注。在这一研究中,首先合成了一种用磺酸和 -Cl 官能团 UiO-66-SO3H-Cl 修饰的新型催化剂,它是一种高效的异相催化剂,具有路易斯酸、布氏酸和 -Cl 官能团结合位点三种官能团的重叠效应,可将葡萄糖转化为 HMF。路易斯酸位点负责将葡萄糖异构化为果糖,而将果糖脱水为 HMF 则由布伦斯特酸位点负责。-Cl基团通过与葡萄糖形成氢键来促进葡萄糖的水解,降低活化能,从而提高 HMF 的生产率。利用 XRD、FT-IR、FE-SEM、EDS 和 XPS 对合成的催化剂进行了分析。通过 EDS 分析,本研究中新合成的催化剂中 Zr、Cl 和 S 元素的含量分别为 37.44%、1.01% 和 6.8%。通过 XPS 分析证实了 UiO-66-SO3H-Cl 中 C 1s (284.8 eV)、O 1s (531.9 eV)、Cl 2p (200.4 eV)、Zr 3d (185.2 eV) 和 S 2p (168.4 eV) 的存在。通过紫外可见光谱分析确定了 UiO-66、UiO-66-SO3H 和 UiO-66-SO3H-Cl 催化剂从葡萄糖制取 5-HMF 的反应范围分别为 10%、23% 和 74%,结果表明具有三个官能团的 UiO-66-SO3H-Cl 催化剂能协同提高葡萄糖的 HMF 产量。 图表摘要 UiO-66-SO3H-Cl 多功能固体催化剂将葡萄糖转化为 HMF:路易斯酸(Zr 阳离子)和布氏酸(SO3H 基团)分别是葡萄糖异构化为果糖和果糖脱水为 HMF 的活性位点。-Cl 基团与葡萄糖形成氢键,提高了 HMF 的生产率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis of UiO-66-SO3H-Cl as the recyclable multifunctional catalyst for efficient conversion of glucose to 5–Hydroxymethylfurfural

5-Hydroxymethylfurfural (HMF), a leading platform combination for altering biomass to diverse biomass-derived chemicals and biofuels, has been engrossed in spacious consideration. In this perusal, a new catalyst modified with sulfonic acid and -Cl functional group UiO-66-SO3H-Cl was first used as an efficiently heterogeneous catalyst with the overlapping effect of three functional groups of Lewis acid, Brønsted acid and -Cl group binding site was synthesized to convert glucose to HMF. The Lewis acid site is responsible for the isomerization of glucose to fructose, and the dehydration of fructose to HMF is the responsibility of the Brønsted acid site. The -Cl group facilitates the hydrolysis of glucose by forming a hydrogen bond with glucose and reducing the activation energy, thus increasing the production rate of HMF. The synthesized catalysts were analyzed using XRD, FT-IR, FE-SEM, EDS, and XPS. The amount of Zr, Cl, and S elements reported in the newly synthesized catalyst in this research by EDS is 37.44%, 1.01%, and 6.8%, respectively. The existence of C 1s (284.8 eV), O 1s (531.9 eV), Cl 2p (200.4 eV), Zr 3d (185.2 eV), and S 2p (168.4 eV) of UiO-66-SO3H-Cl was confirmed by conducting XPS analysis. The reaction range of 5-HMF produced from glucose by each of UiO-66, UiO-66-SO3H, and UiO-66-SO3H-Cl catalysts, was 10%, 23% and 74%, respectively, as determined by UV-Vis analysis was decided the results show that the UiO-66-SO3H-Cl catalyst with three functional groups synergistically increases the production of HMF from glucose.

Graphical Abstract

Conversion of glucose to HMF by UiO-66-SO3H-Cl multifunctional solid catalyst: Lewis acid (Zr cation) and Brønsted acid (SO3H group) are active sites for isomerizing glucose to fructose and dehydration of fructose to HMF, respectively. The -Cl group forms a hydrogen bond with glucose, increasing the production rate of HMF.

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来源期刊
Journal of Chemical Sciences
Journal of Chemical Sciences CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
3.10
自引率
5.90%
发文量
107
审稿时长
1 months
期刊介绍: Journal of Chemical Sciences is a monthly journal published by the Indian Academy of Sciences. It formed part of the original Proceedings of the Indian Academy of Sciences – Part A, started by the Nobel Laureate Prof C V Raman in 1934, that was split in 1978 into three separate journals. It was renamed as Journal of Chemical Sciences in 2004. The journal publishes original research articles and rapid communications, covering all areas of chemical sciences. A significant feature of the journal is its special issues, brought out from time to time, devoted to conference symposia/proceedings in frontier areas of the subject, held not only in India but also in other countries.
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