Abstract
Red onion skin extract and quercetin dihydrate modified with 2-aminophenol were used as adsorbents to extract Cu2+, Ni2+ and Zn2+ from their aqueous solutions. The unmodified and modified adsorbents were characterized using some physicochemical parameters such as melting point, solubility in different solvents, thin layer chromatography and FTIR. The FTIR revealed presence of various functional groups in the structure of modified and unmodified red onion skin extract and quercetin dihydrate. Extraction studies result showed that the maximum pH for metal removal is 3.30, 8.00 and 6.46 for Cu2+, Ni2+ and Zn2+ respectively. The percentage removal and adsorption capacities of the metal ions increased with increasing contact time, dosage and metal ion concentration. Quercetin dihydrate-diazonium salt (QDDS) showed a higher percentage removal for Cu2+ (99.19 %) than Ni2+ and Zn2+ while Red onions skin extract- diazonium salt (ROSEDS) showed a similar percentage removal for Cu2+ (98.57%) > Ni2+ (84.51%) > Zn (66.86%). Heavy metal ions were removed in this order; Cu2+ (99.19%) > Ni2+ (87.64%) > Zn2+ (71.56%) using QDDS. The adsorption kinetic studies and isotherm studies indicated that Pseudo-second order kinetics and Freundlich isotherm model best describe the adsorption processes. Therefore, ROSEDS and QDDS have proven to be an effective adsorbent for heavy metal ions from waste waters and industrial effluents.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: Scholars International Journal of Chemistry and Material Sciences
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.