SO3H, Cl和Cr3+功能化碳C (Cr, Cl, S)的制备:葡萄糖高效转化为5-羟甲基糠醛的可回收多功能催化剂

IF 2.5 4区 化学 Q2 Engineering
Molood Falsafin, Kamal Ghani, Arash Shokrollahi
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引用次数: 0

摘要

羟甲基糠醛(HMF)是合成高价值衍生物的重要可再生平台化学品。虽然从生物质中生产HMF已经引起了极大的兴趣,但优化生产成本、能源效率和环境影响之间的权衡仍然是一个关键的挑战。利用碳基固体酸催化剂将葡萄糖催化转化为HMF为生产这种战略平台分子提供了一条可持续和有效的途径。在氯化铬(CrCl3)存在下,以共碳化淀粉和聚氯乙烯(PVC)为原料,通过磺化反应合成了一种新型催化剂C (Cr, Cl, S)。该催化剂具有Brønsted酸(-SO3H)和Lewis酸(Cr3+)位点,它们协同促进葡萄糖异构化为果糖,随后果糖脱水为HMF。值得注意的是,-Cl基团通过与-OH基团的强相互作用增强葡萄糖的吸附,从而拉伸碳框架并降低底物与催化剂之间的位阻。用XPS、FE-SEM、EDS和FT-IR对C (Cr, Cl, S)催化剂进行了表征。XPS分析证实了关键官能团的存在,其结合能分别为C 1s (284.6 eV)、O 1s (532.1 eV)、Cl 2p (200.1 eV)、Cr 2p (575.5 eV)和S 2p (168.4 eV),分别对应于Lewis酸位点(Cr3+)、Brønsted酸位点(-SO3H)和结合位点(-Cl)。EDX定量分析显示其元素组成为Cr(7.47%)、Cl(3.30%)和S(5.11%)。在优化条件下,该催化剂的HMF产率达到88%(通过紫外可见光谱量化),表明其具有可扩展生物质转化的潜力。C (Cr, Cl, S)多功能固体催化剂将葡萄糖转化为HMF涉及两个活性位点:Lewis酸位点(Cr阳离子)促进葡萄糖异构化成果糖,而Brønsted酸位点(SO3H基团)促进果糖脱水成HMF。此外,-Cl基团与葡萄糖形成氢键,提高了HMF的生成速度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preparation of SO3H, Cl and Cr3+ functionalized carbon C (Cr, Cl, S): a recyclable multifunctional catalyst for efficient glucose conversion to 5-hydroxymethylfurfural

Hydroxymethylfurfural (HMF) is a pivotal renewable platform chemical for synthesizing high-value derivatives. While the production of HMF from biomass has garnered significant interest, optimizing the trade-offs among production costs, energy efficiency, and environmental impact remains a critical challenge. The catalytic conversion of glucose to HMF using carbon-based solid acid catalysts offers a sustainable and efficient route for producing this strategic platform molecule. In this study, a novel catalyst, C (Cr, Cl, S), was synthesized via sulfonation of co-carbonized starch and polyvinyl chloride (PVC) in the presence of chromium (III) chloride (CrCl3). The catalyst features both Brønsted acid (–SO3H) and Lewis acid (Cr3+) sites, which synergistically promote glucose isomerization to fructose and subsequent fructose dehydration to HMF. Notably, the –Cl groups enhance glucose adsorption by strongly interacting with its –OH groups, thereby stretching the carbon framework and reducing steric hindrance between the substrate and catalyst. The C (Cr, Cl, S) catalyst was thoroughly characterized by XPS, FE-SEM, EDS, and FT-IR. XPS analysis confirmed the presence of key functional groups, with binding energies at C 1s (284.6 eV), O 1s (532.1 eV), Cl 2p (200.1 eV), Cr 2p (575.5 eV), and S 2p (168.4 eV), corresponding to Lewis acid sites (Cr3+), Brønsted acid sites (–SO3H), and binding sites (–Cl). EDX quantification revealed elemental compositions of Cr (7.47%), Cl (3.30%), and S (5.11%). Under optimized conditions, the catalyst achieved an exceptional HMF yield of 88% (quantified by UV–Vis spectroscopy), demonstrating its potential for scalable biomass conversion.

Graphical abstract

The conversion of glucose to HMF using the C (Cr, Cl, S) multifunctional solid catalyst involves two active sites: the Lewis acid site (Cr cation) facilitates the isomerization of glucose to fructose, while the Brønsted acid site (SO3H group) promotes the dehydration of fructose to HMF. Additionally, the –Cl group forms a hydrogen bond with glucose, enhancing the HMF production rate.

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来源期刊
Chemical Papers
Chemical Papers Chemical Engineering-General Chemical Engineering
CiteScore
3.30
自引率
4.50%
发文量
590
期刊介绍: Chemical Papers is a peer-reviewed, international journal devoted to basic and applied chemical research. It has a broad scope covering the chemical sciences, but favors interdisciplinary research and studies that bring chemistry together with other disciplines.
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