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Study of Pb (II) adsorption from aqueous solutions by TiO2 functionalized with hydroxide ethyl aniline (PHEA/n-TiO2)

In this study, the crystalline Nano particles of TiO2 were modified with hydroxide ethyl aniline and were used for the elimination of Pb (II) ions from the liquid solutions. The adsorbent was synthesized via chemical oxidization method and characterized by FTIR, SEM and XRD analysis. Variations in p...

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Bibliographic Details
Published in:Journal of molecular liquids 2018-08, Vol.263, p.294-302
Main Authors: Yousefzadeh, H., Salarian, A.A., Sid Kalal, H.
Format: Article
Language:English
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Summary:In this study, the crystalline Nano particles of TiO2 were modified with hydroxide ethyl aniline and were used for the elimination of Pb (II) ions from the liquid solutions. The adsorbent was synthesized via chemical oxidization method and characterized by FTIR, SEM and XRD analysis. Variations in pH, adsorbent dosage, initial metal ion concentration, contact time, temperature and ionic strength were considered as the effective parameters on the adsorbent performance in batch mode adsorption. Optimum condition was cleared through the batch experiments as follow: pH = 5.5, adsorbent dosage = 2 g L−1, initial concentration of Pb (II) ions = 100 mg L−1, temperature = 328 k, contact time = 3 h and agitation speed = 150 rpm. The maximum adsorption capacity under the optimum conditions was obtained 26.05 mg g−1. Webber-Morris model and Langmuir isotherm were the best mathematical models for prediction of kinetic and equilibrium behavior, respectively. Thermodynamic studies demonstrate that the adsorption of Pb (II) ions is spontaneous and endothermic. •TiO2 nanoparticles as the adsorbent were modified with Poly Hydroxide Ethyl Aniline.•Adsorbent was characterized with SEM, FTIR and XRD analysis.•Adsorption Optimum condition was at pH 5.5, temperature 328 k, contact time 3 h.•The maximum adsorption capacity was obtained 26.05 mg g−1.•Langmuir isotherm was suitable to describe of adsorbent equilibrium behavior.
ISSN:0167-7322
1873-3166
DOI:10.1016/j.molliq.2018.03.023