Investigation of the Properties of Mo/ZSM-5 Catalysts Based on Zeolites with Microporous and Micro–Mesoporous Structures

Abstract

The dehydroaromatization of methane (MDA) is of great interest as a promising process for processing natural and associated petroleum gases, the main component of which is methane. The rapid loss of catalyst activity because of coke formation hinders the introduction of the DHA methane process into the industry. Therefore, the aim of this research was to find ways to improve Mo/ZSM-5 catalysts for MDA. The paper presents the results of the synthesis of high-silica zeolites of the ZSM-5 type with microporous and micro–mesoporous structures, the preparation of Mo/ZSM-5 catalysts based on them, and the study of the physicochemical and catalytic properties of the obtained samples during the non-oxidative conversion of methane into aromatic hydrocarbons. Zeolite catalysts were investigated using IR spectroscopy, X-ray diffraction, TPD-NH3, SEM, HR-TEM, and N2 adsorption. It was found that the addition of carbon black in the stage of the synthesis of zeolite type ZSM-5 did not lead to structural changes, and the obtained samples had a crystallinity degree equal to 100%. The creation of the micro–mesoporous structure in Mo/ZSM-5 catalysts led to an increase in their activity and stability in the process of methane dehydroaromatization. The highest conversion of methane was observed on a 4.0%Mo/ZSM-5 catalyst prepared based on zeolite synthesized using 1.0% carbon black and was 13.0% after 20 min of reaction, while the benzene yield reached 7.0%. It was shown using HR-TEM that a more uniform distribution of the active metal component was observed in a zeolite catalyst with a micro–mesoporous structure than in a microporous zeolite.

Materials Enabling Methane and Toluene Gas Treatment

“…Throughout the methane dehydrogenation process, the Mo/ZSM-5 catalysts' stability and activity are increased by their capacity to take on a microporous form. The 4.0 percent Mo/ZSM-5 catalyst developed utilizing zeolite synthesized from 1.0% carbon black displayed the greatest transformation of methane, achieving 13 percent after 20 min, and benzene synthesis, reaching 7.0% [48]. In order to create 4%Mo/ZSM-5 catalysts for the non-oxidative conversion of methane to aromatic hydrocarbons, Stepanov et al examined the impact of secondary mesoporous structure formation in ZSM-5 zeolites on the catalytic characteristics of those catalysts.…”