4.4 Article

Nanostructured Functionalised Niobium Oxide as Chemoselective Catalyst for Acetalation of Glucose

Journal

TOPICS IN CATALYSIS
Volume 65, Issue 19-20, Pages 1994-2004

Publisher

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s11244-022-01738-8

Keywords

Acetalation; Niobium oxide; Sulfate groups; Glucose; Ethyl glucosides

Funding

  1. Newton Bhabha PhD placement program
  2. British Council
  3. University Grants Commission, New Delhi, India

Ask authors/readers for more resources

This study focuses on synthesizing sulfate functionalized niobium oxide-based catalyst for the acetalation of biomass-derived glucose. The results show that the sulfate groups incorporated NbOx-DS catalyst exhibits superior catalytic activity and selectivity compared to commercial niobium oxide catalyst (NbOx-CS). The study highlights the importance of the synthesis procedure for efficient incorporation of sulfate groups.
Developing a chemoselective catalyst for the acetalation of biomass-derived glucose to alkyl glycosides has been recognised as an emerging field due to its wide range of applications. The present study focuses on synthesising sulfate functionalised niobium oxide-based (NbOx-DS) catalyst to introduce medium/strong acidic sites that contribute to the catalytic activity towards glucose acetalation, which has not been explored previously. The nanosized NbOx-D is prepared via a precipitation approach using niobium chloride and diethylamine as a precursor and precipitating agent, respectively. The sulfate groups incorporated NbOx-DS gives a good yield of ethyl glucosides (60%) with excellent selectivity (97%) in ethanol. On the other hand, the sulfate groups incorporated into the commercial niobium oxide (NbOx-CS) exhibits poor catalytic activity, yielding 6% ethyl glucoside with a low selectivity (8%). FTIR analysis corroborates the incorporation of sulfate groups in the NbOx-DS matrix, unlike NbOx-CS. XRD pattern of NbOx-DS shows a lower angle shift of a peak to 23.5 degrees compared to parent NbOx-D (24.32 degrees), indicating lattice expansion due to the incorporation of sulfate groups, and no such a shift in the case of NbOx-CS is observed. NH3-temperature programmed desorption (NH3-TPD) reveals that NbOx-DS possess a 2.1-fold higher number of acidic sites than NbOx-D, whereas NbOx-CS possess a negligible number of acidic sites, indicating the significance of the synthesis procedure of NbOx-D for efficient incorporation of sulfate groups. NbOx-DS displays recyclability for at least three runs with minor loss in the activity. In a nutshell, the current study reflects that NbOx-DS obtained via precipitation followed by sulfate groups incorporation increases the medium/strong acidic sites, which contributes significantly to enhancing the ethyl glucoside selectivity (97%). [GRAPHICS] .

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