Wander Y. Perez-Sena , Maëlle Paya , Kari Eränen , Robert Lassfolk , Lucas Lagerquist , Narendra Kumar , Atte Aho , Antonio D'Angelo , Tapio Salmi , Johan Wärnå , Dmitry Yu. Murzin
{"title":"铌催化剂上过氧化氢对糠醛的异相催化氧化作用","authors":"Wander Y. Perez-Sena , Maëlle Paya , Kari Eränen , Robert Lassfolk , Lucas Lagerquist , Narendra Kumar , Atte Aho , Antonio D'Angelo , Tapio Salmi , Johan Wärnå , Dmitry Yu. Murzin","doi":"10.1039/d3cy01686b","DOIUrl":null,"url":null,"abstract":"<div><p>Furfural is a very interesting bio-based platform molecule that can be derived from the pentoses found in hemicelluloses, such as xylose and arabinose. Furfural displays significant potential as a source for the production of various chemicals. By oxidizing furfural with hydrogen peroxide, a range of products can be obtained, including diacids such as succinic and maleic acids, as well as lactones such as 2(5<em>H</em>)-furanone. In this study, the oxidation of furfural was conducted using niobia as a heterogeneous catalyst, which displayed an interesting behavior, giving 2,3-dihydroxybutanedioic acid (tartaric acid) as the main oxidation product. Other typical oxidation products, namely succinic acid and 2(5<em>H</em>)-furanone were also obtained in moderate concentrations. Tartaric acid and the rest of the oxidation products were identified by GS-MS, <sup>1</sup>H NMR and <sup>13</sup>C NMR. A wide range of conditions were screened to reveal the catalytic behavior of the system, enabling furfural consumption and formation of tartaric acid. Additionally, a plausible reaction network was established based on a previously proposed mechanism and experimental observations that accounted for the production of tartaric acid.</p></div>","PeriodicalId":66,"journal":{"name":"Catalysis Science & Technology","volume":"14 7","pages":"Pages 1942-1957"},"PeriodicalIF":4.2000,"publicationDate":"2024-04-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Heterogeneous catalytic oxidation of furfural with hydrogen peroxide over a niobia catalyst†\",\"authors\":\"Wander Y. Perez-Sena , Maëlle Paya , Kari Eränen , Robert Lassfolk , Lucas Lagerquist , Narendra Kumar , Atte Aho , Antonio D'Angelo , Tapio Salmi , Johan Wärnå , Dmitry Yu. Murzin\",\"doi\":\"10.1039/d3cy01686b\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Furfural is a very interesting bio-based platform molecule that can be derived from the pentoses found in hemicelluloses, such as xylose and arabinose. Furfural displays significant potential as a source for the production of various chemicals. By oxidizing furfural with hydrogen peroxide, a range of products can be obtained, including diacids such as succinic and maleic acids, as well as lactones such as 2(5<em>H</em>)-furanone. In this study, the oxidation of furfural was conducted using niobia as a heterogeneous catalyst, which displayed an interesting behavior, giving 2,3-dihydroxybutanedioic acid (tartaric acid) as the main oxidation product. Other typical oxidation products, namely succinic acid and 2(5<em>H</em>)-furanone were also obtained in moderate concentrations. Tartaric acid and the rest of the oxidation products were identified by GS-MS, <sup>1</sup>H NMR and <sup>13</sup>C NMR. A wide range of conditions were screened to reveal the catalytic behavior of the system, enabling furfural consumption and formation of tartaric acid. Additionally, a plausible reaction network was established based on a previously proposed mechanism and experimental observations that accounted for the production of tartaric acid.</p></div>\",\"PeriodicalId\":66,\"journal\":{\"name\":\"Catalysis Science & Technology\",\"volume\":\"14 7\",\"pages\":\"Pages 1942-1957\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2024-04-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Catalysis Science & Technology\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S2044475324001643\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Catalysis Science & Technology","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2044475324001643","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Heterogeneous catalytic oxidation of furfural with hydrogen peroxide over a niobia catalyst†
Furfural is a very interesting bio-based platform molecule that can be derived from the pentoses found in hemicelluloses, such as xylose and arabinose. Furfural displays significant potential as a source for the production of various chemicals. By oxidizing furfural with hydrogen peroxide, a range of products can be obtained, including diacids such as succinic and maleic acids, as well as lactones such as 2(5H)-furanone. In this study, the oxidation of furfural was conducted using niobia as a heterogeneous catalyst, which displayed an interesting behavior, giving 2,3-dihydroxybutanedioic acid (tartaric acid) as the main oxidation product. Other typical oxidation products, namely succinic acid and 2(5H)-furanone were also obtained in moderate concentrations. Tartaric acid and the rest of the oxidation products were identified by GS-MS, 1H NMR and 13C NMR. A wide range of conditions were screened to reveal the catalytic behavior of the system, enabling furfural consumption and formation of tartaric acid. Additionally, a plausible reaction network was established based on a previously proposed mechanism and experimental observations that accounted for the production of tartaric acid.
期刊介绍:
A multidisciplinary journal focusing on cutting edge research across all fundamental science and technological aspects of catalysis.
Editor-in-chief: Bert Weckhuysen
Impact factor: 5.0
Time to first decision (peer reviewed only): 31 days