Abstract
Selective hydrogenation catalysts play a key role in many industrial processes, but they are primarily based on supported noble metals, such as Pt and Pd, which are usually dispersed in nanoparticles. However, the production and recovery of these noble metal nanoparticles is a very energy-consuming and expensive procedure. Accordingly, replacing these metals by other inexpensive, transition metals such as Fe and Cu without sacrificing the activity and selectivity, will necessarily reduce their production costs. Moreover, zeolites as a support provide the advantage of shape selectivity to the desired product. In this study, we develop an alternative method for preparing hydrogenation catalysts composed of metallic nanoparticles encapsulated into zeolite frameworks through reductive demetallation of Fe-zeolites or Cu/Fe-zeolites with MFI topology. Particularly, the process of reductive demetallation is described using temperature-programmed reduction (TPR) and Mössbauer spectroscopy data. The reductive demetallation of Fe-MFI, consisting of Fe extraction from the zeolite framework and formation of Fe0 nanoparticles, starts at the temperatures above 800 ℃ and finishes at 1030 ℃, when sintering occurs strongly. In contrast, introduction of second metal leads to the decrease in the reduction temperature, as process of CuFe@MFI formation finishes at 800 ℃. Both Fe@MFI and CuFe@MFI show activity in p-nitrotoluene hydrogenation to p-toluidine. Conversion of the substrate grows with increase in the Cu and Fe loading. Thus, this synthesis method of encapsulation of Fe0 nanoparticles and Fe0-Cu0 bimetallic nanoparticles into the zeolite micropores through reductive demetallation of Fe-zeolites can be used to prepare hydrogenation catalysts.
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