Catalytic Conversion of Biomass-Derived 5-Hydroxymethylfurfural Into 2,5-Bis(hydroxymethyl)furan Using Hierarchically Hortensia-Like α-Ni(OH)2 Without Prereduction
{"title":"Catalytic Conversion of Biomass-Derived 5-Hydroxymethylfurfural Into 2,5-Bis(hydroxymethyl)furan Using Hierarchically Hortensia-Like α-Ni(OH)2 Without Prereduction","authors":"Shimao Gao, Mengyao Xu, Yufei Huang, Weixing Pan, Aicheng Chen","doi":"10.1002/kin.70006","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Inexpensive hierarchically hortensia-like α-Ni(OH)<sub>2</sub> catalysts without prereduction were introduced to the 5-hydroxymethylfurfural (HMF) hydrogenation to 2,5-bis(hydroxymethyl)furan (BHMF) via the catalytic transfer hydrogenation (CTH) process. Given the catalytic performance evaluated on the hortensia-like α-Ni(OH)<sub>2</sub>, the catalyst of Ni(OH)<sub>2</sub>-OLA synthesized using an oleylamine-assisted solvothermal method has prospective in the HMF hydrogenation to BHMF. A remarkable 95.96% of the BHMF selectivity with 96.81% of the HMF conversion was obtained on Ni(OH)<sub>2</sub>-OLA at 135°C for 5 h under N<sub>2</sub> atmosphere using the ethanol as the hydrogen donor. Based on the kinetic analysis, the lowest activation energy of 39.6 kJ·mol<sup>−1</sup> and the highest preexponential factor of 19.1 s<sup>−1</sup> could be found on Ni(OH)<sub>2</sub>-OLA, which revealed the superior catalytic performance in the HMF hydrogenation to BHMF over Ni(OH)<sub>2</sub>-OLA. Moreover, excellent stability and reusability also could be found on Ni(OH)<sub>2</sub>-OLA, which indicated that the hortensia-like α-Ni(OH)<sub>2</sub> catalysts have the potential for industrialization. The findings of this study provide an efficient catalyst system with low-cost and high-performance for the HMF hydrogenation via the CTH process.</p>\n </div>","PeriodicalId":13894,"journal":{"name":"International Journal of Chemical Kinetics","volume":"57 10","pages":"615-624"},"PeriodicalIF":1.6000,"publicationDate":"2025-07-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Chemical Kinetics","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/kin.70006","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Inexpensive hierarchically hortensia-like α-Ni(OH)2 catalysts without prereduction were introduced to the 5-hydroxymethylfurfural (HMF) hydrogenation to 2,5-bis(hydroxymethyl)furan (BHMF) via the catalytic transfer hydrogenation (CTH) process. Given the catalytic performance evaluated on the hortensia-like α-Ni(OH)2, the catalyst of Ni(OH)2-OLA synthesized using an oleylamine-assisted solvothermal method has prospective in the HMF hydrogenation to BHMF. A remarkable 95.96% of the BHMF selectivity with 96.81% of the HMF conversion was obtained on Ni(OH)2-OLA at 135°C for 5 h under N2 atmosphere using the ethanol as the hydrogen donor. Based on the kinetic analysis, the lowest activation energy of 39.6 kJ·mol−1 and the highest preexponential factor of 19.1 s−1 could be found on Ni(OH)2-OLA, which revealed the superior catalytic performance in the HMF hydrogenation to BHMF over Ni(OH)2-OLA. Moreover, excellent stability and reusability also could be found on Ni(OH)2-OLA, which indicated that the hortensia-like α-Ni(OH)2 catalysts have the potential for industrialization. The findings of this study provide an efficient catalyst system with low-cost and high-performance for the HMF hydrogenation via the CTH process.
期刊介绍:
As the leading archival journal devoted exclusively to chemical kinetics, the International Journal of Chemical Kinetics publishes original research in gas phase, condensed phase, and polymer reaction kinetics, as well as biochemical and surface kinetics. The Journal seeks to be the primary archive for careful experimental measurements of reaction kinetics, in both simple and complex systems. The Journal also presents new developments in applied theoretical kinetics and publishes large kinetic models, and the algorithms and estimates used in these models. These include methods for handling the large reaction networks important in biochemistry, catalysis, and free radical chemistry. In addition, the Journal explores such topics as the quantitative relationships between molecular structure and chemical reactivity, organic/inorganic chemistry and reaction mechanisms, and the reactive chemistry at interfaces.