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Efficient dehydrogenation of a formic acid–ammonium formate mixture over Au(3)Pd(1) catalyst

A series of AuPd/C catalysts were prepared and tested for the first time for active and stable dehydrogenation of a formic acid–ammonium formate (FA–AF) mixture. The catalysts with different Au-to-Pd molar ratios were prepared using a facile simultaneous reduction method and characterized using tran...

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Detalles Bibliográficos
Autores principales: Guo, Xiao-Tong, Zhang, Juan, Chi, Jian-Chao, Li, Zhi-Hui, Liu, Yu-Chen, Liu, Xin-Ru, Zhang, Shu-Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9060862/
https://www.ncbi.nlm.nih.gov/pubmed/35517262
http://dx.doi.org/10.1039/c8ra09534e
Descripción
Sumario:A series of AuPd/C catalysts were prepared and tested for the first time for active and stable dehydrogenation of a formic acid–ammonium formate (FA–AF) mixture. The catalysts with different Au-to-Pd molar ratios were prepared using a facile simultaneous reduction method and characterized using transmission electron microscopy (TEM), high-resolution TEM, energy dispersive X-ray spectroscopy, X-ray diffraction, and X-ray photoelectron spectroscopy. It was found that the catalytic activity and stability of the Au(3)Pd(1)/C catalyst was the best. The initial turnover frequency for the dehydrogenation of the FA–AF mixture over the Au(3)Pd(1)/C catalyst can reach 407.5 h(−1) at 365 K. The reaction order with respect to FA and AF is 0.25 and 0.55, respectively. The apparent activation energy of dehydrogenation is 23.3 ± 1.3 kJ mol(−1). The catalytic activity of the Au(3)Pd(1)/C catalyst remains ca. 88.0% after 4 runs, which is much better than the single Pd/C catalyst. The mechanism for the dehydrogenation is also discussed.