Metal nanocatalysts confined within hydrophobic zeolite for selective hydrogenation of nitroaromatics
DOI: 10.23977/analc.2024.030104 | Downloads: 2 | Views: 74
Author(s)
Zhongshan Zhao 1, Yue Sun 1, Tao Cai 1
Affiliation(s)
1 College of Chemistry and Chemical Engineering, Qingdao University, Qingdao, China
Corresponding Author
Yue SunABSTRACT
This study focuses on the encapsulation of palladium-based nanocatalysts within Silicalite-1 zeolite through in-situ synthesis, with an aim to enhance the selective hydrogenation of nitroaromatic compounds. By controlling the size of palladium metal nanoclusters to approximately 1nm and incorporating hydrophobic organic groups into the zeolite framework, we significantly improved the hydrogenation efficiency. The modification with hydrophobic groups, specifically methyl groups, not only augmented the hydrophobicity of the zeolite but also its catalytic performance, especially for Pd@S-1-CH3, in the hydrogenation of nitrobenzene, surpassing that of Pd@S-1. This modification was instrumental in achieving enhanced performance due to the improved mass transfer of reactants within the zeolite pores. The catalytic activity and stability of the modified catalysts were thoroughly investigated, with Pd@S-1-CH3 demonstrating considerable activity and selectivity across various nitrobenzene derivatives. Notably, after 10 reaction cycles, the catalyst maintained high conversion rates and selectivity for 4-fluoronitrobenzene, underlining its robustness. This research provides valuable insights into the design of highly efficient and stable nanocatalysts for the selective hydrogenation of nitroaromatic compounds, offering a promising approach for the synthesis of aromatic amines, crucial intermediates in the chemical industry.
KEYWORDS
Zeolite; Metal nanocatalysts; Limiting effect; Selective hydrogenation; Aromatic amineCITE THIS PAPER
Zhongshan Zhao, Yue Sun, Tao Cai, Metal nanocatalysts confined within hydrophobic zeolite for selective hydrogenation of nitroaromatics. Analytical Chemistry: A Journal (2024) Vol. 3: 20-25. DOI: http://dx.doi.org/10.23977/analc.2024.030104.
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