Synthesis, Characterization, and Evaluation of the Adsorption Behavior of Cellulose-Graft-Poly Heavy Metals
In this study, the synthesis and characterization of grafted cellulose fiber with binary monomers mixture obtained using a KMnO[sub.4] /citric acid redox initiator were investigated. Acrylonitrile (AN) was graft copolymerized with acrylic acid (AA) and styrene (Sty) at different monomer ratios with...
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Veröffentlicht in: | Polymers 2024-02, Vol.16 (3) |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | In this study, the synthesis and characterization of grafted cellulose fiber with binary monomers mixture obtained using a KMnO[sub.4] /citric acid redox initiator were investigated. Acrylonitrile (AN) was graft copolymerized with acrylic acid (AA) and styrene (Sty) at different monomer ratios with evaluating percent graft yield (GY%). Cell-g-P(AN-co-AA) and Cell-g-P(AN-co-Sty) were characterized by SEM, FT-IR, [sup.13] C CP MAS NMR, TGA, and XRD. An AN monomer was used as principle-acceptor monomer, and GY% increases with AN ratio up to 60% of total monomers mixture volume. The adsorption behaviors of Cell-g-P(AN-co-AA) and Cell-g-P(AN-co-Sty) were studied for the adsorption of Ni(II) and Cu(II) metal ions from aqueous solution. Optimal adsorption conditions were determined, including 8 h contact time, temperature of 30 °C, and pH 5.5. Cell-g-P(AN-co-AA) showed maximum adsorption capacity of 435.07 mg/g and 375.48 mg/g for Ni(II) and Cu(II), respectively, whereas Cell-g-P(AN-co-Sty) showed a maximum adsorption capacity of 379.2 mg/g and 349.68 mg/g for Ni(II) and Cu(II), respectively. Additionally, adsorption equilibrium isotherms were studied, and the results were consistent with the Langmuir model. The Langmuir model’s high determinant coefficient (R[sup.2] ) predicted monolayer sorption of metal ions. Consequently, Cell-g-P(AN-co-AA) and Cell-g-P(AN-co-Sty) prepared by a KMnO[sub.4] /citric acid initiator were found to be efficient adsorbents for heavy metals from wastewater as an affordable and adequate alternative. |
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ISSN: | 2073-4360 2073-4360 |
DOI: | 10.3390/polym16030445 |