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Photocatalytic Epoxidation of Propylene with Bi2WO6-Based Catalyst Supported on Glass Beads

Received: 6 September 2022    Accepted: 29 October 2022    Published: 31 March 2023
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Abstract

The photo activities of some photo-catalysts including TiO2, Bi2WO6 and Bi2WO6-TiO2 (in various mixing ratios) were evaluated for photo-epoxidation of propylene. The photocatalytic epoxidation reaction was performed in gas-phase under atmospheric pressure. Typical reaction mixture of C3H6:O2:N2 corresponding to the ratio 1:1:18, afforded PO (PO) in addition to other products such as acetone, acetaldehyde and propanal as observed by the FTIR-GCMS tandem analysis. It was established from the results that Bi2WO6-TiO2 photo-catalysts were more preferable for selectivity of PO peaking at 49%. The highest formation rate of PO achieved was 111μmol g cat-1 h-1 over 12mol% Bi2WO6-TiO2 ratio in a typical flow reaction for 1h at 345 K under UVA illumination. Under this condition the selectivity of products was also observed to be very stable. Further study on the effect of light intensity revealed that increasing the light intensity from 0.1 to 0.3mWcm-2 significantly increased the selectivity of PO by 5%. Higher intensity depreciated the PO selectivity. In order to study the effect of temperature on the photocatalytic epoxidation reaction, a systematic approach was followed. As raising the reaction temperature influences the distribution of products significantly, a temperature range of 335-355 K was used in the optimised reaction condition. At 355 K, it was observed that the formation of propanal was favoured which was attributed to its inhibition to be transformed into propionic acid. However, raising the reaction temperature was observed to affect the rate of reaction in two ways: first, the adsorption of PR on to the photo-catalyst which causes a decrease in the reaction efficiency was reduced and secondly, the desorption of products of reaction which in turn reveals more active sites, was improved.

Published in American Journal of Physical Chemistry (Volume 12, Issue 1)
DOI 10.11648/j.ajpc.20231201.12
Page(s) 7-16
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This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Propylene, Photo-Catalysis, Photo-Oxidation, Propylene Oxide, Photo-Reactor

References
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[6] N. Li, B. Yang, M. Liu, Y. Chen, and J. Zhou, “Synergetic photo-epoxidation of propylene with molecular oxygen over bimetallic Au–Ag/TS-1 photocatalysts,” Chinese J. Catal., vol. 38, no. 5, pp. 831–843, May 2017.
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[13] V. A. Patil, J. A. Liburdy, and J. Homepage, “Turbulent flow characteristics in a randomly packed porous bed based on particle image velocimetry measurements Additional information on Phys. Fluids Turbulent flow characteristics in a randomly packed porous bed based on particle image velocimetry measurements,” Cit. Phys. Fluids, vol. 25, p. 43304, 2013.
[14] A. V. Vorontsov, D. V. Kozlov, P. G. Smirniotis, and V. N. Parmon, “TiO2 photocatalytic oxidation: II. Gas-phase processes,” Kinet. Catal., vol. 46, no. 3, pp. 422–436, 2005.
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    Emmanuel Alhassan Kamba, Qiao Chen. (2023). Photocatalytic Epoxidation of Propylene with Bi2WO6-Based Catalyst Supported on Glass Beads. American Journal of Physical Chemistry, 12(1), 7-16. https://doi.org/10.11648/j.ajpc.20231201.12

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    ACS Style

    Emmanuel Alhassan Kamba; Qiao Chen. Photocatalytic Epoxidation of Propylene with Bi2WO6-Based Catalyst Supported on Glass Beads. Am. J. Phys. Chem. 2023, 12(1), 7-16. doi: 10.11648/j.ajpc.20231201.12

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    AMA Style

    Emmanuel Alhassan Kamba, Qiao Chen. Photocatalytic Epoxidation of Propylene with Bi2WO6-Based Catalyst Supported on Glass Beads. Am J Phys Chem. 2023;12(1):7-16. doi: 10.11648/j.ajpc.20231201.12

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  • @article{10.11648/j.ajpc.20231201.12,
      author = {Emmanuel Alhassan Kamba and Qiao Chen},
      title = {Photocatalytic Epoxidation of Propylene with Bi2WO6-Based Catalyst Supported on Glass Beads},
      journal = {American Journal of Physical Chemistry},
      volume = {12},
      number = {1},
      pages = {7-16},
      doi = {10.11648/j.ajpc.20231201.12},
      url = {https://doi.org/10.11648/j.ajpc.20231201.12},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajpc.20231201.12},
      abstract = {The photo activities of some photo-catalysts including TiO2, Bi2WO6 and Bi2WO6-TiO2 (in various mixing ratios) were evaluated for photo-epoxidation of propylene. The photocatalytic epoxidation reaction was performed in gas-phase under atmospheric pressure. Typical reaction mixture of C3H6:O2:N2 corresponding to the ratio 1:1:18, afforded PO (PO) in addition to other products such as acetone, acetaldehyde and propanal as observed by the FTIR-GCMS tandem analysis. It was established from the results that Bi2WO6-TiO2 photo-catalysts were more preferable for selectivity of PO peaking at 49%. The highest formation rate of PO achieved was 111μmol g cat-1 h-1 over 12mol% Bi2WO6-TiO2 ratio in a typical flow reaction for 1h at 345 K under UVA illumination. Under this condition the selectivity of products was also observed to be very stable. Further study on the effect of light intensity revealed that increasing the light intensity from 0.1 to 0.3mWcm-2 significantly increased the selectivity of PO by 5%. Higher intensity depreciated the PO selectivity. In order to study the effect of temperature on the photocatalytic epoxidation reaction, a systematic approach was followed. As raising the reaction temperature influences the distribution of products significantly, a temperature range of 335-355 K was used in the optimised reaction condition. At 355 K, it was observed that the formation of propanal was favoured which was attributed to its inhibition to be transformed into propionic acid. However, raising the reaction temperature was observed to affect the rate of reaction in two ways: first, the adsorption of PR on to the photo-catalyst which causes a decrease in the reaction efficiency was reduced and secondly, the desorption of products of reaction which in turn reveals more active sites, was improved.},
     year = {2023}
    }
    

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  • TY  - JOUR
    T1  - Photocatalytic Epoxidation of Propylene with Bi2WO6-Based Catalyst Supported on Glass Beads
    AU  - Emmanuel Alhassan Kamba
    AU  - Qiao Chen
    Y1  - 2023/03/31
    PY  - 2023
    N1  - https://doi.org/10.11648/j.ajpc.20231201.12
    DO  - 10.11648/j.ajpc.20231201.12
    T2  - American Journal of Physical Chemistry
    JF  - American Journal of Physical Chemistry
    JO  - American Journal of Physical Chemistry
    SP  - 7
    EP  - 16
    PB  - Science Publishing Group
    SN  - 2327-2449
    UR  - https://doi.org/10.11648/j.ajpc.20231201.12
    AB  - The photo activities of some photo-catalysts including TiO2, Bi2WO6 and Bi2WO6-TiO2 (in various mixing ratios) were evaluated for photo-epoxidation of propylene. The photocatalytic epoxidation reaction was performed in gas-phase under atmospheric pressure. Typical reaction mixture of C3H6:O2:N2 corresponding to the ratio 1:1:18, afforded PO (PO) in addition to other products such as acetone, acetaldehyde and propanal as observed by the FTIR-GCMS tandem analysis. It was established from the results that Bi2WO6-TiO2 photo-catalysts were more preferable for selectivity of PO peaking at 49%. The highest formation rate of PO achieved was 111μmol g cat-1 h-1 over 12mol% Bi2WO6-TiO2 ratio in a typical flow reaction for 1h at 345 K under UVA illumination. Under this condition the selectivity of products was also observed to be very stable. Further study on the effect of light intensity revealed that increasing the light intensity from 0.1 to 0.3mWcm-2 significantly increased the selectivity of PO by 5%. Higher intensity depreciated the PO selectivity. In order to study the effect of temperature on the photocatalytic epoxidation reaction, a systematic approach was followed. As raising the reaction temperature influences the distribution of products significantly, a temperature range of 335-355 K was used in the optimised reaction condition. At 355 K, it was observed that the formation of propanal was favoured which was attributed to its inhibition to be transformed into propionic acid. However, raising the reaction temperature was observed to affect the rate of reaction in two ways: first, the adsorption of PR on to the photo-catalyst which causes a decrease in the reaction efficiency was reduced and secondly, the desorption of products of reaction which in turn reveals more active sites, was improved.
    VL  - 12
    IS  - 1
    ER  - 

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Author Information
  • Chemical Sciences Department, Federal University Wukari, Wukari, Nigeria

  • Chemistry Department, School of Life Sciences, University of Sussex, Brighton, UK

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