Structure sensitivity of Cu supported on manganese oxide catalysts in levulinic acid hydrogenation

Nayan Jyoti Mazumdar, Praveen Kumar, Miryam Arredondo-Arechavala, Nancy Artioli, Haresh Manyar*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)
27 Downloads (Pure)

Abstract

Different synthesis methods were used to prepare a series of size-controlled copper nanoparticles supported on manganese oxide octahedral molecular sieve (OMS-2) catalysts. All Cu/OMS-2 catalysts, with average Cu nanoparticle sizes prepared in the range of 2-22 nm, were thoroughly characterised using X-ray diffraction (XRD), N2 sorption, H2 temperature programmed reduction (TPR), transmission electron microscopy (TEM), and ICP-OES elemental analyses. The catalytic activity of the size-controlled Cu/OMS-2 catalysts was investigated in liquid phase hydrogenation of levulinic acid as a model reaction to evaluate the nanoparticle size dependance and structure-activity relationship. The catalytic activity studies showed that the catalyst performance depends greatly on the catalyst preparation methodology and Cu nanoparticle size. Complete conversion of levulinic acid with a high γ-valerolactone yield, >99%, was observed using Cu/OMS-2 catalysts prepared by the precipitation-deposition (Cu nanoparticle size 2-3 nm) method. In comparison to wet-impregnated catalysts (Cu particle size 20-22 nm), the improved performance of precipitation-deposition catalysts was mainly attributed to the well-distributed, smaller Cu nanoparticles. The influence of Cu nanoparticle size is correlated with the turnover frequency (TOF, h−1) for levulinic acid conversion, indicating the structure sensitivity of the levulinic acid hydrogenation reaction.

Original languageEnglish
Pages (from-to)840-849
Number of pages10
JournalCatalysis Science & Technology
Volume14
Issue number4
Early online date15 Dec 2023
DOIs
Publication statusPublished - Feb 2024

Bibliographical note

Funding Information:
The authors gratefully acknowledge the financial support for PhD studentship to N. J. M. funded through the collaboration initiative between Queen's University Belfast and Tezpur University, India. H. M. also acknowledges the funding and support provided by the Leverhulme Trust research grant RPG-2020-301, as well as the UK Catalysis hub via the authors' membership in the UK Catalysis Hub Consortium funded by EPSRC grant: EP/R026645/1.

Publisher Copyright:
© 2024 The Royal Society of Chemistry.

ASJC Scopus subject areas

  • Catalysis

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