Performance Analysis of Effective Methylene Blue Immobilization by Carbon Microspheres Obtained from Hydrothermally Processed Fructose.

Bibliographic Details
Title: Performance Analysis of Effective Methylene Blue Immobilization by Carbon Microspheres Obtained from Hydrothermally Processed Fructose.
Authors: Krstić, Sanja S., Čokeša, Đuro, Vujasin, Radojka T., Kaluđerović, Branka V., Momčilović, Milan Z., Jaćimovski, Darko, Gurikov, Pavel, Dodevski, Vladimir M.
Source: Processes; Dec2024, Vol. 12 Issue 12, p2683, 14p
Subject Terms: X-ray powder diffraction, CARBON-based materials, SCANNING electron microscopy, HYDROTHERMAL carbonization, SURFACES (Technology), METHYLENE blue
Abstract: Carbon microspheres have been synthesized by the hydrothermal method with fructose and a phosphoric acid solution at two different concentrations, which were used as precursors. The obtained materials were characterized by elemental analysis, X-ray powder diffraction (XRPD) analysis, scanning electron microscopy (SEM), nitrogen adsorption/desorption measurements, and Fourier transform infrared (FTIR) spectroscopy. Batch sorption experiments were performed to remove methylene blue (MB) from aqueous solutions by varying the initial concentration of MB (C0) from 50 to 500 mg/dm3, contact period, solution pH value, and temperature. Prepared sorbents consisted of microsphere particles with diameters in the range of 0.6–2.7 µm. The synthetic route was found to govern the microporous–mesoporous structure and surface acidic functional groups of the final product. A phosphoric acid concentration of 40 wt.% gave carbon material with a specific surface area of 932 m2/g and a total pore volume of 0.43 cm3/g. It was found that the extent of MB sorption by the obtained carbon microspheres increased with initial dye concentration, contact time, and especially solution pH but slightly decreased with increasing temperature. Kinetic studies showed that the dye sorption process followed pseudo-second-order kinetics. [ABSTRACT FROM AUTHOR]
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Database: Complementary Index
More Details
ISSN:22279717
DOI:10.3390/pr12122683
Published in:Processes
Language:English