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Selective glucose oxidation to glucaric acid using bimetallic catalysts: Lattice expansion or electronic structure effect?

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    SYSNO ASEP0578834
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleSelective glucose oxidation to glucaric acid using bimetallic catalysts: Lattice expansion or electronic structure effect?
    Author(s) Lavrič, Ž. (SI)
    Teržan, J. (SI)
    Kroflič, A. (SI)
    Zavašnik, J. (SI)
    Olszówka, Joanna Elżbieta (UFCH-W) ORCID
    Vajda, Štefan (UFCH-W) RID, ORCID
    Huš, M. (SI)
    Grilc, M. (SI)
    Likozar, B. (SI)
    Article number123455
    Source TitleApplied Catalysis B - Environmental. - : Elsevier - ISSN 0926-3373
    Roč. 343, APR 2024 (2024)
    Number of pages15 s.
    Languageeng - English
    CountryNL - Netherlands
    Keywordsglucaric acid ; glucose oxidation ; catalyst characterization ; DFT
    Subject RIVCF - Physical ; Theoretical Chemistry
    OECD categoryPhysical chemistry
    R&D ProjectsGF21-48595L GA ČR - Czech Science Foundation (CSF)
    Method of publishingOpen access
    Institutional supportUFCH-W - RVO:61388955
    UT WOS001118493200001
    EID SCOPUS85178013559
    DOI10.1016/j.apcatb.2023.123455
    AnnotationOur study presents a comprehensive approach for the selective oxidation of glucose to glucaric acid (GA) by heterogeneous catalysis. We have synthesized and characterized Au/ZrO2, AuCu/ZrO2 and AuPt/ZrO2 catalysts using X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and oxygen pulse chemisorption (OPS) techniques. Combining experimental observations with in-depth density functional theory (DFT) studies, we found that bimetallic catalysts form alloys, which exhibit different characteristics than monometallic counterparts for the given reaction. We performed batch reactions, varying temperature and oxygen pressure, and used the data to construct a predictive microkinetic model. As it turned out, AuPt/ZrO2 showed the highest selectivity, yielding 32% of GA at 100 °C and 30 barg O2. Our results provide valuable insights for the developing of efficient catalysts and point out the bottlenecks for the oxidation of glucose to GA.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2025
    Electronic addresshttps://hdl.handle.net/11104/0347751
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