{"title":"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","authors":"Molood Falsafin, Kamal Ghani, Arash Shokrollahi","doi":"10.1007/s12039-023-02245-3","DOIUrl":null,"url":null,"abstract":"<div><p>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-SO<sub>3</sub>H-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-SO<sub>3</sub>H, and UiO-66-SO<sub>3</sub>H-Cl catalysts, was 10%, 23% and 74%, respectively, as determined by UV-Vis analysis was decided the results show that the UiO-66-SO<sub>3</sub>H-Cl catalyst with three functional groups synergistically increases the production of HMF from glucose.</p><h3>Graphical Abstract</h3><p>Conversion of glucose to HMF by UiO-66-SO<sub>3</sub>H-Cl multifunctional solid catalyst: Lewis acid (Zr cation) and Brønsted acid (SO<sub>3</sub>H 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.\n</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":616,"journal":{"name":"Journal of Chemical Sciences","volume":null,"pages":null},"PeriodicalIF":1.7000,"publicationDate":"2024-02-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis of UiO-66-SO3H-Cl as the recyclable multifunctional catalyst for efficient conversion of glucose to 5–Hydroxymethylfurfural\",\"authors\":\"Molood Falsafin, Kamal Ghani, Arash Shokrollahi\",\"doi\":\"10.1007/s12039-023-02245-3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>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-SO<sub>3</sub>H-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-SO<sub>3</sub>H, and UiO-66-SO<sub>3</sub>H-Cl catalysts, was 10%, 23% and 74%, respectively, as determined by UV-Vis analysis was decided the results show that the UiO-66-SO<sub>3</sub>H-Cl catalyst with three functional groups synergistically increases the production of HMF from glucose.</p><h3>Graphical Abstract</h3><p>Conversion of glucose to HMF by UiO-66-SO<sub>3</sub>H-Cl multifunctional solid catalyst: Lewis acid (Zr cation) and Brønsted acid (SO<sub>3</sub>H 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.\\n</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>\",\"PeriodicalId\":616,\"journal\":{\"name\":\"Journal of Chemical Sciences\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2024-02-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Chemical Sciences\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s12039-023-02245-3\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Sciences","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s12039-023-02245-3","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
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.
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.