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Basic thermodynamic characteristics of toluene adsorption in Cu<sup>2+</sup>ZSM-5 Zeolite

Khayot BakhronovTashkent University of Information Technologies named after Muhammad al-Khwarazmi, 108 Amir Temur Avenue, 100200, Tashkent, UzbekistanOybek ErgashevNamangan Institute of Engineering and Technology, 7 Kasansay Street, 160115, Namangan, UzbekistanNazirahon EsonkulovaNamangan Institute of Engineering and Technology, 7 Kasansay Street, 160115, Namangan, UzbekistanIlmira AbsalyamovaTashkent University of Information Technologies named after Muhammad al-Khwarazmi, 108 Amir Temur Avenue, 100200, Tashkent, UzbekistanMajidjon AhkmadovTashkent University of Information Technologies named after Muhammad al-Khwarazmi, 108 Amir Temur Avenue, 100200, Tashkent, Uzbekistan
E3S Web of Conferencesjournal2023en
ABI

Аннотация

This paper presents the results of isotherms and basic (ΔH, ΔF and ΔS) thermodynamic characteristics of toluene adsorption in CuZSM-5 zeolite. For measurements of isotherms and differential heat of adsorption, a system consisting of a universal high-vacuum adsorption unit and an attached differential modified Tian-Calve microcalorimeter DAC-1-1A was used to provide direct quantitative and qualitative characteristics of the nature and forces of adsorption interaction. The correlation between the adsorption-energy characteristics wasfound and the molecular mechanismof toluene adsorption in CuZSM-5 zeolite in the whole filling region was revealed. Toluene adsorbed in CuZSM-5 zeolite is located in the first coordination sphere with Cu 2+ cation, forming two-dimensional complexes. It was found that the charge density significantly affects the mechanism, the energy of adsorption and the number of adsorbed molecules. It was determined that the average molar entropy of toluene adsorption in CuZSM5 zeolite indicates that the mobility of toluene molecules in zeolite is below the liquid phase and close to that of the solid phase, indicating that the mobility of toluene molecules on cations is strongly inhibited. This work shows how calorimetric data can be used to complement crystal structure results and detect subtle adsorbent/adsorbate interactions at the molecular level.

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