Issue 18, 2023, Issue in Progress

Selective adsorption of anionic and cationic dyes on mesoporous UiO-66 synthesized using a template-free sonochemistry method: kinetic, isotherm and thermodynamic studies

Abstract

In this study, template-free mesoporous UiO-66(U) has been successfully synthesized in shortened time by sonochemical methods and provided energy savings. The synthesized mesoporous UiO-66(U) demonstrated irregular morphology particle around 43.5 nm according to the SEM image. The N2 adsorption–desorption isotherm indicated an irregular, 8.88 nm pore width mesoporous structure. Ultrasonic irradiation waves greatly altered mesoporous materials. A mechanism for mesoporous UiO-66(U) formation has been proposed based on the present findings. Sonochemical-solvent heat saves 97% more energy than solvothermal. Mesoporous UiO-66(U) outperformed solvothermal-synthesized UiO-66(S) in adsorption. These studies exhibited that mesopores in UiO-66 promote dye molecule mass transfer (MO, CR, and MB). According to kinetics and adsorption isotherms, the pseudo-second-order kinetic and Langmuir isotherm models matched experimental results. Thermodynamic studies demonstrated that dye adsorption is spontaneous and exothermically governed by entropy, not enthalpy. Mesoporous UiO-66(U) also showed good anionic dye selectivity in mixed dye adsorption. Mesoporous UiO-66(U) may be regenerated four times while maintaining strong adsorption capability.

Graphical abstract: Selective adsorption of anionic and cationic dyes on mesoporous UiO-66 synthesized using a template-free sonochemistry method: kinetic, isotherm and thermodynamic studies

Supplementary files

Article information

Article type
Paper
Submitted
02 Nov 2022
Accepted
10 Apr 2023
First published
20 Apr 2023
This article is Open Access
Creative Commons BY license

RSC Adv., 2023,13, 12320-12343

Selective adsorption of anionic and cationic dyes on mesoporous UiO-66 synthesized using a template-free sonochemistry method: kinetic, isotherm and thermodynamic studies

A. R. Putra Hidayat, L. L. Zulfa, A. R. Widyanto, R. Abdullah, Y. Kusumawati and R. Ediati, RSC Adv., 2023, 13, 12320 DOI: 10.1039/D2RA06947D

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