Reactivity of mesoporous ZSM-5 zeolite towards Friedel-Crafts acylation of anisole and propionic anhydride
DOI:
https://doi.org/10.11113/mjcat.v2n2.70Keywords:
mesoporous ZSM-5 zeolite, microporous ZSM-5, mesoporous, aluminosilicate, Friedel-Crafts acylation reactionAbstract
Â
ZSM-5 zeolite is known as solid acid catalyst for many organic reactions. ZSM-5 zeolite is a microporous aluminosilicate catalyst which is not suitable for reactions involving large molecules. Therefore, ZSM-5 with mesopores size needs to be synthesized. In this study, mesoporous ZSM-5 were synthesized in the presence and absence of sucrose as mesotemplate. As comparison, microporous ZSM-5 was also synthesized using standard method. The samples were characterized using XRD, FTIR and nitrogen adsorption analysis. Results from XRD and FTIR of sample with sucrose template showed the formation of crystalline ZSM-5 structure while sample without sucrose showed amorphous phase. Nitrogen adsorption analysis showed that the synthesized mesoporous ZSM-5 has mesoporous structure with type IV isotherm which the average pore is in the range of 4-6 nm and the BET surface area was 400 m2/g. The reactivity of all synthesized samples was tested in Friedel-Craft acylation of anisole and propionic anhydride to produce the main product, p-methoxypropiophenone and the side product, propionic acid. Results proved that synthesized mesoporous ZSM-5 with sucrose is the best catalyst in term of conversion and selectivity with 73.66% and 80.45% respectively as compared to sample without sucrose has comparable selectivity, 75.11% but low conversion, 22.63%. In contrast, microporous ZSM-5 has comparable conversion, 80.81% but low selectivity, 55.53%. This indicates that acidity and mesoporosity are responsible enhanced reactivity of ZSM-5 catalyst for Friedel-Crafts reaction involving large molecule.
References
Ruthven, D. M. (1984). Principles of Adsorption and Adsorption Processes. Canada: John Wiley & Sons. Publication.
Wang, D., Zhang, L., Chen, L., Wu, H., & Wu, P. (2015). Postsynthesis of Mesoporous ZSM-5 Zeolite by Piperidine-assisted Desilication and its Superior Catalytic Properties in Hydrocarbon Cracking. J. Mater. Chem. A, 3(7), 3511–3521.
Zhao, J., Yin, Y., Li, Y., Chen, W., & Liu, B. (2015). Synthesis and Characterization of Mesoporous Zeolite Y by using Block Copolymers as Templates. Chemical Engineering Journal, 284, 405–411.
Ma, Y., Hu, J., Jia, L., Li, Z., Kan, Q., & Wu, S. (2013). Synthesis, Characterization and Catalytic Activity of a Novel Mesoporous ZSM-5 Zeolite. Materials Research Bulletin, 48(5), 1881–1884. Zhou, M., Rownaghi, A. A., & Hedlund, J. (2013). Synthesis of Mesoporous ZSM-5 Zeolite Crystals by Conventional Hydrothermal Treatment. The Royal Society of Chemistry.
Jin, L., Xie, T., Liu, S., Li, Y., & Hu, H. (2016). Controllable Synthesis Of Chainlike Hierarchical ZSM-5 Templated By Sucrose And Its Catalytic Performance. CATCOM, 75, 32–3.
Ma, Y., Hu, J., Jia, L., Li, Z., Kan, Q., & Wu, S. (2013). Synthesis, Characterization and Catalytic Activity of a Novel Mesoporous ZSM-5 Zeolite. Materials Research Bulletin, 48(5), 1881–1884.
Tracey, M. J., Higgins, J. B., & Ballmoos, R. von. (1996). Collection Of Simulated XRD Powder Patterns For Zeolites. Amsterdam: Elsevier Inc.
Kadja, G. T., Mukti, R. R., Liu, Z., Rilyanti, M., I., Marsih, I. N., . Okubo, T. (2016). Mesoporogen-free synthesis of hierarchically porous ZSM-5 below 100°C. Microporous and Mesoporous Materials, 226, 344-352. doi:10.1016/j.micromeso.2016.02.007
Downloads
Published
How to Cite
Issue
Section
License
The Malaysian Journal of Catalysis publishes open access articles under the terms of the Creative Commons Attribution (CC BY) License which permits use, distribution and reproduction in any medium, provided the original work is properly cited.Â
The Department of Chemistry, Faculty of Science, UTM retains the Copyright on any research article published by Malaysian Journal of Catalysis.
Authors grant Malaysian Journal of Catalysis a license to publish the article and identify itself as the original publisher.