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Adsorption Study of Lead Ions on Nickel-Metal Organic Framework
Corresponding Author(s) : Patience Mapule Thabede
Asian Journal of Chemistry,
Vol. 31 No. 5 (2019): Vol 31 Issue 5
Abstract
Nickel(II) based metal-organic framework (MOF) was synthesized using terephthalic acid, C6H4(COOH)2 as an organic linker. This MOF was characterized and used as an adsorbent for the removal of lead ions in aqueous medium. Characterization was conducted by X-ray diffraction, Fourier transform infrared spectroscopy, thermal gravimetric analysis and scanning electron microscopy techniques. The removal of Pb2+ ions from aqueous medium varied with contact time, concentration, pH and temperature.
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References
N.D. Shooto, C.W. Dikio, D. Wankasi and L.M. Sikhwivhilu, Chem. Sci. J., 6, 4 (2015); https://doi.org/10.4172/2150-3494.1000113.
D.T. Sun, L. Peng, W.S. Reeder, S.M. Moosavi, D. Tiana, D.K. Britt, E. Oveisi and W.L. Queen, ACS Cent.Sci.,4, 349 (2018); https://doi.org/10.1021/acscentsci.7b00605.
A. Maleki, B. Hayati, M. Naghizadeh and S.W. Joo, J. Ind. Eng. Chem., 28, 211 (2015); https://doi.org/10.1016/j.jiec.2015.02.016.
N.A. Khan and S.H. Jhung, J. Hazard. Mater., 325, 198 (2017); https://doi.org/10.1016/j.jhazmat.2016.11.070.
Y. Peng, H. Huang, Y. Zhang, K. Chufan, C. Chen, S. Song, L. Liu and C. Zhong, Nature Commun., 187 (2018); https://doi.org/10.1038/s41467-017-02600-2.
N.D. Shooto, E.D. Dikio, D. Wankasi and L.M. Sikhwivhilu, Hem. Ind., 17, 221 (2017); https://doi.org/10.2298/HEMIND160120032S.
E.M. Gama, A.S. Lima and V.A. Lemos, J. Hazard. Mater., 136, 757 (2006); https://10.1016/j.jhazmat.2006.01.015.
M.R. Sohrabi, Z. Matbouie, A.A. Asgharinezhad and A. Dehghani, Microchim. Acta, 180, 589 (2013); https://doi.org/10.1007/s00604-013-0952-4.
H. Saleem, U. Rafique and R.S. Davies, Micropor. Mesopor. Mater., 221, 238 (2016); https://doi.org/10.1016/j.micromeso.2015.09.043.
N.D. Rudd, H. Wang, E.M.A. Fuentes-Fernandez, S.J. Teat, F. Chen, G. Hall, Y.J. Chabal and J. Li, ACS Appl. Mater. Interfaces, 8, 30294 (2016); https://doi.org/10.1021/acsami.6b10890.
Q.-R. Fang, D.-Q. Yuan, J. Sculley, J.-R. Li, Z.-B. Han and H.-C. Zhou, Inorg. Chem., 49, 11637 (2010); https://doi.org/10.1021/ic101935f.
F. Ke, L.-G. Qiua, Y.-P. Yuana, F.-M. Penga, X. Jianga, A.-J. Xiea, Y.- H. Shena and J.-F. Zhub, J. Hazard. Mater., 96, 36 (2011); https://doi.org/10.1016/j.jhazmat.2011.08.069.
N.D. Shooto, C.W. Dikio, D. Wankasi, L.M. Sikhwivhilu, F.M. Mtunzi and E.D. Dikio, Nanoscale Res. Lett., 11, 414 (2016); https://doi.org/10.1186/s11671-016-1631-2.
N. Mohammadi and F. Manteghi, Sciforum: The 19th International Electronic Conference on Synthesis Organic Chemistry I (2015); https://doi.org/10.3390/ecsoc-19-a047.
S. Zhao, D. Chen, F. Wei, N. Chen, Z. Liang and Y. Luo, Ultrason. Sonochem., 39, 845 (2017); https://doi.org/10.1016/j.ultsonch.2017.06.013.
B. Maranescu, L. Lupa and A. Visa, Pure Appl. Chem., 90, 35 (2018); https://doi.org/10.1515/pac-2017-0307.