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Valorisation of rhodamine B adsorbed copolymer beads for the recovery of Cu2+ from e-waste: Green approach

Publication Type : Journal Article

Publisher : Journal of Environmental Chemical Engineering

Source : Journal of Environmental Chemical Engineering, Elsevier Ltd, Volume 6, Number 6, p.7002-7009 (2018)

Url : https://www.scopus.com/inward/record.uri?eid=2-s2.0-85056669761&doi=10.1016%2fj.jece.2018.10.054&partnerID=40&md5=4c811797e9600f7a6baffe40653ab305

Keywords : acetone, adsorption, Adsorption parameters, Copolymer beads, Copper compounds, Electrolytic solution, Electronic Waste, Ion exchange, Langmuir adsorption isotherms, Methacrylic acids, Microscopic analysis, recovery, Rhodamine B, Rhodium compounds, Suspension polymerization, Suspensions (fluids), Wastes

Campus : Coimbatore

School : School of Engineering

Department : Sciences

Year : 2018

Abstract : The methacrylic acid-divinylbenzene copolymer beads were prepared by suspension polymerization and used for the removal of rhodamine B (RhB) dye. Batch experiments were carried out to find the adsorption parameters. Langmuir adsorption isotherm model was found to be the best suited for the adsorption of RhB on the copolymer beads. The RhB adsorbed copolymer beads were valorised as adsorbent for the removal of Cu2+ from e-waste solution, which was compared with electrolytic solution. The Cu2+ loaded on the RhB containing copolymer beads was recovered by using 1 M HNO3. The RhB loaded on the copolymer beads were successfully eluted by using a mixture of acetone and acetic acid. Selectivity of RhB dye for the recovery of Cu2+ ions from e-waste was also carried out in this work. Methods were developed to recover both the Cu2+ and RhB dye separately. Microscopic analysis was performed to understand the adsorption of RhB and ion-exchange of Cu2+ onto the copolymer beads. © 2018 Elsevier Ltd.

Cite this Research Publication : K. K. Arun Viswan and Dr. Gangadharan D., “Valorisation of rhodamine B adsorbed copolymer beads for the recovery of Cu2+ from e-waste: Green approach”, Journal of Environmental Chemical Engineering, vol. 6, pp. 7002-7009, 2018.

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