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Facile synthesis and optimization of Acacia senegal gum hydrogel for kinetically treated adsorptive removal of targeted industrial effluents. | LitMetric

Facile synthesis and optimization of Acacia senegal gum hydrogel for kinetically treated adsorptive removal of targeted industrial effluents.

Int J Biol Macromol

Chemistry Department, College of Science, Jouf University, P.O. Box: 2014, Sakaka, Saudi Arabia; Chemistry Department, Faculty of Science, Assiut University, P.O. Box: 71515, Assiut, Egypt.

Published: November 2024

This context summarizes a detail on the fabrication of Acacia senegal Gum Hydrogel (ASGh) within well-engineered microemulsion, and thereafter chemical modification for environmental remediation. In brief, Divinylsulfone was used to crosslink polymeric chains and produce ASGh in ˂50 μm size within the reverse-microemulsion of Natrium-bis-(2-ethylhexyl) sulfosuccinate in gasoline. ASGh were subjected to chemical modification via versatile diethylenetriamine to produce m-[ASGh] for adsorptive removal of methyl orange (MO), eosin Y (EY) and congo red (CR) from waste-water. ASGh and m-[ASGh] were characterized through Scanning Electron Microscopy (SEM), Fourier Transform Infrared Spectroscopy (FTIR), and zeta potential measurements. For instance, FT-IR spectra depicted new bands upon Diethylenetriamine modification. The zeta potential measurements confirm a positively charged surface of m-[ASGh] upon Diethylenetriamine addition. Interestingly, 0.05 g m-[ASGh] demonstrated 91.0, 84.1, and 73.0 % removal efficiency towards MO, EY and CR, respectively in 2 h equilibrium time. Langmuir, Freundlich and modified-Freundlich isotherms were applied to further delineate adsorption data. Modified-Freundlich model depicted comparatively more agreeable fit, and delivered R value nearer to unity. Further, 143 mg·g, 130 mg·g and, 116 mg·g maximum adsorption capacity (Q) was represented by m-[ASGh] towards MO, EY and CR, respectively in 2 h. Interestingly, real water sample were tested whereby, the Q against MO, EY and CR was 146 mg·g, 132 mg·g and, 111 mg·g, respectively in 2 h equilibrium time. To conclude, m-[ASGh] could be treated as decolorizing agent in real waste-water polluted through negatively charged organic pollutants, particularly MO.

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Source
http://dx.doi.org/10.1016/j.ijbiomac.2024.134879DOI Listing

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