Yongjia Liang, Jianliang Zuo*, Zhaohao Cai, Weican Huang, Jing Lin and Zili Liu*,
{"title":"稀土金属改性co基催化剂在糠醛高选择性加氢制1,5-戊二醇中的应用","authors":"Yongjia Liang, Jianliang Zuo*, Zhaohao Cai, Weican Huang, Jing Lin and Zili Liu*, ","doi":"10.1021/acs.iecr.4c0438210.1021/acs.iecr.4c04382","DOIUrl":null,"url":null,"abstract":"<p >The ability to effectively control furan ring opening is the key to transforming furfural into 1,5-pentanediol. Herein, a series of Co-based catalysts modified with rare-earth metals (Y, Pr, La, and Ce) were synthesized. It was found that Y-modified Co-based catalyst with a Co/Y molar ratio of 3.5/0.5 exhibited the highest selectivity for 1,5-pentanediol (53.7%) at 150 °C and 4 MPa H<sub>2</sub> in isopropanol (time = 5 h). Coordination between Co and Y in the catalyst resulted in more CoO<sub><i>x</i></sub> and oxygen vacancies, which are vital factors for cleaving the C–O bond of the furan ring. In addition, highly dispersed small-sized Co<sup>0</sup> particles on the catalyst surface could boost the dissociation of H<sub>2</sub> molecules, which attacked the carbonyl group in the furan ring of furfural to afford 1,5-pentanediol. Density functional theory calculations revealed that the presence of CoO<sub><i>x</i></sub>/Y<sub>2</sub>O<sub>3</sub> oxide interfaces promoted adsorption of furfural (especially via the furan ring) and hydrogenolysis during the hydrogenation process. Modifying a Co-based catalyst with rare-earth metals offers a novel approach for producing 1,5-pentanediol from furfural.</p>","PeriodicalId":39,"journal":{"name":"Industrial & Engineering Chemistry Research","volume":"64 14","pages":"7220–7231 7220–7231"},"PeriodicalIF":3.9000,"publicationDate":"2025-03-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Rare-Earth Metal Modified Co-Based Catalysts for Highly Selective Hydrogenation of Furfural to 1,5-Pentanediol\",\"authors\":\"Yongjia Liang, Jianliang Zuo*, Zhaohao Cai, Weican Huang, Jing Lin and Zili Liu*, \",\"doi\":\"10.1021/acs.iecr.4c0438210.1021/acs.iecr.4c04382\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The ability to effectively control furan ring opening is the key to transforming furfural into 1,5-pentanediol. Herein, a series of Co-based catalysts modified with rare-earth metals (Y, Pr, La, and Ce) were synthesized. It was found that Y-modified Co-based catalyst with a Co/Y molar ratio of 3.5/0.5 exhibited the highest selectivity for 1,5-pentanediol (53.7%) at 150 °C and 4 MPa H<sub>2</sub> in isopropanol (time = 5 h). Coordination between Co and Y in the catalyst resulted in more CoO<sub><i>x</i></sub> and oxygen vacancies, which are vital factors for cleaving the C–O bond of the furan ring. In addition, highly dispersed small-sized Co<sup>0</sup> particles on the catalyst surface could boost the dissociation of H<sub>2</sub> molecules, which attacked the carbonyl group in the furan ring of furfural to afford 1,5-pentanediol. Density functional theory calculations revealed that the presence of CoO<sub><i>x</i></sub>/Y<sub>2</sub>O<sub>3</sub> oxide interfaces promoted adsorption of furfural (especially via the furan ring) and hydrogenolysis during the hydrogenation process. Modifying a Co-based catalyst with rare-earth metals offers a novel approach for producing 1,5-pentanediol from furfural.</p>\",\"PeriodicalId\":39,\"journal\":{\"name\":\"Industrial & Engineering Chemistry Research\",\"volume\":\"64 14\",\"pages\":\"7220–7231 7220–7231\"},\"PeriodicalIF\":3.9000,\"publicationDate\":\"2025-03-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Industrial & Engineering Chemistry Research\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.iecr.4c04382\",\"RegionNum\":3,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENGINEERING, CHEMICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Industrial & Engineering Chemistry Research","FirstCategoryId":"5","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.iecr.4c04382","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
Rare-Earth Metal Modified Co-Based Catalysts for Highly Selective Hydrogenation of Furfural to 1,5-Pentanediol
The ability to effectively control furan ring opening is the key to transforming furfural into 1,5-pentanediol. Herein, a series of Co-based catalysts modified with rare-earth metals (Y, Pr, La, and Ce) were synthesized. It was found that Y-modified Co-based catalyst with a Co/Y molar ratio of 3.5/0.5 exhibited the highest selectivity for 1,5-pentanediol (53.7%) at 150 °C and 4 MPa H2 in isopropanol (time = 5 h). Coordination between Co and Y in the catalyst resulted in more CoOx and oxygen vacancies, which are vital factors for cleaving the C–O bond of the furan ring. In addition, highly dispersed small-sized Co0 particles on the catalyst surface could boost the dissociation of H2 molecules, which attacked the carbonyl group in the furan ring of furfural to afford 1,5-pentanediol. Density functional theory calculations revealed that the presence of CoOx/Y2O3 oxide interfaces promoted adsorption of furfural (especially via the furan ring) and hydrogenolysis during the hydrogenation process. Modifying a Co-based catalyst with rare-earth metals offers a novel approach for producing 1,5-pentanediol from furfural.
期刊介绍:
ndustrial & Engineering Chemistry, with variations in title and format, has been published since 1909 by the American Chemical Society. Industrial & Engineering Chemistry Research is a weekly publication that reports industrial and academic research in the broad fields of applied chemistry and chemical engineering with special focus on fundamentals, processes, and products.