Pb2+ and Cd2+ recovery from water using residual tea waste and SiO2@TW nanocomposites

dc.contributor.authorJoshi, S
dc.contributor.authorKataria, N
dc.contributor.authorGarg, V.K
dc.contributor.authorKadirvelu, K.
dc.date.accessioned2020-07-16T07:41:52Z
dc.date.accessioned2024-08-14T06:39:20Z
dc.date.available2020-07-16T07:41:52Z
dc.date.available2024-08-14T06:39:20Z
dc.date.issued2020
dc.description.abstractThis work reports the fabrication of SiO2@TW nanocomposites and their application for Pb2+ and Cd2+ ions sequestration from simulated water. Residual tea waste has also been used for metal ions sequestration to compare the potential of SiO2@TW nanocomposites. The SEM, TEM, BET, FTIR and EDX techniques were employed for the characterization of SiO2@TW nanocomposites and residual tea waste. Particle sizes of SiO2@TW nanocomposites was in the range of 6.8-12 nm. The experiments were carried out in batch mode to explore the effect of various operating parameters on the sequestration of Pb2+ and Cd2+ ions from water. The experimental data was subjected to various thermodynamic, kinetic and isothermic models. According to Langmuir model, the maximum adsorption efficiency of the SiO2@TW nanocomposites was 153 mg/g for Pb2+ and 222 mg/g for Cd2+ but maximum adsorption efficiency of residual tea waste for Pb2+ was 125 mg/g and for Cd2+ was 142.9 mg/g. This study suggested that due to the presence of active sites SiO2@TW nanocomposites has greater potential for metal sequestration than residual tea waste. 2020 Elsevier Ltden_US
dc.identifier.doi10.1016/j.chemosphere.2020.127277
dc.identifier.issn456535
dc.identifier.urihttps://kr.cup.edu.in/handle/32116/2631
dc.identifier.urlhttps://www.sciencedirect.com/science/article/abs/pii/S0045653520314703
dc.language.isoen_USen_US
dc.publisherElsevieren_US
dc.subjectAdsorptionen_US
dc.subjectHeavy metalsen_US
dc.subjectIsothermsen_US
dc.subjectKineticsen_US
dc.subjectNanocompositesen_US
dc.subjectStober methoden_US
dc.titlePb2+ and Cd2+ recovery from water using residual tea waste and SiO2@TW nanocompositesen_US
dc.title.journalChemosphereen_US
dc.typeArticleen_US
dc.type.accesstypeClosed Accessen_US

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