{"title":"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","authors":"Molood Falsafin, Kamal Ghani, Arash Shokrollahi","doi":"10.1007/s11696-025-04298-9","DOIUrl":null,"url":null,"abstract":"<div><p>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 (CrCl<sub>3</sub>). The catalyst features both Brønsted acid (–SO<sub>3</sub>H) and Lewis acid (Cr<sup>3+</sup>) 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 1<i>s</i> (284.6 eV), O 1<i>s</i> (532.1 eV), Cl 2<i>p</i> (200.1 eV), Cr 2<i>p</i> (575.5 eV), and S 2<i>p</i> (168.4 eV), corresponding to Lewis acid sites (Cr<sup>3+</sup>), Brønsted acid sites (–SO<sub>3</sub>H), 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.</p><h3>Graphical abstract</h3><p>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 (SO<sub>3</sub>H group) promotes the dehydration of fructose to HMF. Additionally, the –Cl group forms a hydrogen bond with glucose, enhancing the HMF production rate.</p>\n<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":513,"journal":{"name":"Chemical Papers","volume":"79 11","pages":"7967 - 7978"},"PeriodicalIF":2.5000,"publicationDate":"2025-08-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Preparation of SO3H, Cl and Cr3+ functionalized carbon C (Cr, Cl, S): a recyclable multifunctional catalyst for efficient glucose conversion to 5-hydroxymethylfurfural\",\"authors\":\"Molood Falsafin, Kamal Ghani, Arash Shokrollahi\",\"doi\":\"10.1007/s11696-025-04298-9\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>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 (CrCl<sub>3</sub>). The catalyst features both Brønsted acid (–SO<sub>3</sub>H) and Lewis acid (Cr<sup>3+</sup>) 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 1<i>s</i> (284.6 eV), O 1<i>s</i> (532.1 eV), Cl 2<i>p</i> (200.1 eV), Cr 2<i>p</i> (575.5 eV), and S 2<i>p</i> (168.4 eV), corresponding to Lewis acid sites (Cr<sup>3+</sup>), Brønsted acid sites (–SO<sub>3</sub>H), 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.</p><h3>Graphical abstract</h3><p>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 (SO<sub>3</sub>H group) promotes the dehydration of fructose to HMF. Additionally, the –Cl group forms a hydrogen bond with glucose, enhancing the HMF production rate.</p>\\n<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>\",\"PeriodicalId\":513,\"journal\":{\"name\":\"Chemical Papers\",\"volume\":\"79 11\",\"pages\":\"7967 - 7978\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2025-08-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Papers\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s11696-025-04298-9\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"Engineering\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Papers","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s11696-025-04298-9","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Engineering","Score":null,"Total":0}
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.
Chemical PapersChemical 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.