{"title":"Epimerization of glucose to rare sugars using Beta zeolite-supported MoOx catalysts","authors":"","doi":"10.1016/j.apcata.2024.119976","DOIUrl":null,"url":null,"abstract":"<div><div>Epimerization of abundant monosaccharides derived from lignocellulosic biomass offers an attractive approach for the synthesis of rare sugars. Molybdenum-based catalysts demonstrate excellent glucose-mannose epimerization performance, but most studies have neglected the synthesis of other sugar epimers and the pathways of their formation. Here, reduced Beta zeolite supported MoO<sub>x</sub> catalysts (Mo/Beta) with 1.5–10 wt% Mo loading were examined for glucose epimerization in water, specifically focusing on the formation of the rare sugars allose and altrose. The physicochemical structure and the catalytic activity of the catalyst were examined in detail, and the reaction mechanisms for the epimer formation were probed by nuclear magnetic resonance (NMR) spectroscopy. The results demonstrate that 5 wt% Mo/Beta achieved a near-equilibrium mannose yield of 30 % from glucose within 10 min at reaction temperatures below 140 °C, exhibiting a relatively low activation energy (∼67 kJ mol<sup>−1</sup>). At elevated reaction temperatures (≥ 120 °C), the rare sugars allose and altrose accumulated to combined yields of 24 % at 140 °C. An isotope labelling study using NMR spectroscopy corroborated the catalysis to involve 1,2-carbon shifts that elicit the formation of rare sugars at sufficiently high temperatures. Evaluation of catalyst reuse and regeneration indicated that supported MoO<sub>x</sub> had higher stability than MoO<sub>3</sub>, but the stability of the Mo/Beta catalysts under hydrothermal conditions leaves room for improvement.</div></div>","PeriodicalId":243,"journal":{"name":"Applied Catalysis A: General","volume":null,"pages":null},"PeriodicalIF":4.7000,"publicationDate":"2024-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied Catalysis A: General","FirstCategoryId":"1","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0926860X24004216","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Epimerization of abundant monosaccharides derived from lignocellulosic biomass offers an attractive approach for the synthesis of rare sugars. Molybdenum-based catalysts demonstrate excellent glucose-mannose epimerization performance, but most studies have neglected the synthesis of other sugar epimers and the pathways of their formation. Here, reduced Beta zeolite supported MoOx catalysts (Mo/Beta) with 1.5–10 wt% Mo loading were examined for glucose epimerization in water, specifically focusing on the formation of the rare sugars allose and altrose. The physicochemical structure and the catalytic activity of the catalyst were examined in detail, and the reaction mechanisms for the epimer formation were probed by nuclear magnetic resonance (NMR) spectroscopy. The results demonstrate that 5 wt% Mo/Beta achieved a near-equilibrium mannose yield of 30 % from glucose within 10 min at reaction temperatures below 140 °C, exhibiting a relatively low activation energy (∼67 kJ mol−1). At elevated reaction temperatures (≥ 120 °C), the rare sugars allose and altrose accumulated to combined yields of 24 % at 140 °C. An isotope labelling study using NMR spectroscopy corroborated the catalysis to involve 1,2-carbon shifts that elicit the formation of rare sugars at sufficiently high temperatures. Evaluation of catalyst reuse and regeneration indicated that supported MoOx had higher stability than MoO3, but the stability of the Mo/Beta catalysts under hydrothermal conditions leaves room for improvement.
期刊介绍:
Applied Catalysis A: General publishes original papers on all aspects of catalysis of basic and practical interest to chemical scientists in both industrial and academic fields, with an emphasis onnew understanding of catalysts and catalytic reactions, new catalytic materials, new techniques, and new processes, especially those that have potential practical implications.
Papers that report results of a thorough study or optimization of systems or processes that are well understood, widely studied, or minor variations of known ones are discouraged. Authors should include statements in a separate section "Justification for Publication" of how the manuscript fits the scope of the journal in the cover letter to the editors. Submissions without such justification will be rejected without review.