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Adsorptive Removal of Anionic Azo Dye Acid Black 194 from Aqueous Solution using NNMBA-Crosslinked Poly N-Vinyl Pyrrolidone Hydrogel
Corresponding Author(s) : Beena Mathew
Asian Journal of Chemistry,
Vol. 32 No. 2 (2020): Vol 32 Issue 2
Abstract
N,N-Methylene bis-acrylamide crosslinked poly-N-vinyl pyrrolidone hydrogels were synthesized and binding of the hydrogel with the dye solution was followed spectrophotometrically. The chemical structure and morphology of the hydrogel before and after adsorption of acid black 194 was confirmed by FT-IR and SEM. Effect of various physico-chemical parameters such as concentration, temperature, pH, time and the amount of hydrogel used were investigated by batch adsorption studies. Hydrogel used as adsorbent in this study was characterized by UV-Vis spectrophotometer before and after adsorption of acid black 194. Kinetic studies suggested pseudo second order reaction. Langmuir and Freundlich isotherms were applied on equilibrium adsorption data and found that Freundlich isotherm fit better for the present investigation. N,N-methylene bisacrylamide crosslinked poly-N-vinyl pyrrolidone hydrogel displayed excellent properties for the removal of the azo dye, acid black 194 from aqueous solution.
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References
Z. Zheng and K. Shetty, J. Agric. Food Chem., 48, 932 (2000); https://doi.org/10.1021/jf9909306.
R. Ganesh, G.D. Boardman and D. Michelsen, Water Res., 28, 1367 (1994); https://doi.org/10.1016/0043-1354(94)90303-4.
K. Selvam, K. Swaminathan and K.S. Chae, World J. Microbiol. Biotechnol., 19, 591 (2003); https://doi.org/10.1023/A:1025128327853.
R. Sebastiano, N. Contiello, S. Senatore, P.G. Righetti and A. Citterio, Dyes Pigments, 94, 258 (2012); https://doi.org/10.1016/j.dyepig.2011.12.014.
K. Wojciechowski and L. Szuster, Comput. Chem., 04, 97 (2016); https://doi.org/10.4236/cc.2016.44010.
J.A. Müller, Water Sci. Technol., 44, 121 (2001); https://doi.org/10.2166/wst.2001.0598.
A. Sienkiewicz, A. Kierys and J. Goworek, J. Dispers. Sci. Technol., 40, 1396 (2018); https://doi.org/10.1080/01932691.2018.1515024.
G.A. Mahmoud, S.E. Abdel-aal, N.A. El-kelesh and E.A. Alshafei, Environ. Ecol. Res., 5, 480 (2017); https://doi.org/10.13189/eer.2017.050703.
R. Parhi, Adv. Pharm. Bull., 7, 515 (2017); https://doi.org/10.15171/apb.2017.064.
J. Maitra, and V. K. Shukla, Am. J. Polym. Sci., 4, 25 (2014); https://doi.org/10.5923/j.ajps.20140402.01.
P. Jerzy and D.C. Neckers, Macromolecules, 18, 1245 (1985); https://doi.org/10.1021/ma00148a035.
M.G. Gigimol and B. Mathew, Polym. Int., 52, 973 (2003); https://doi.org/10.1002/pi.1156.
V.P. Mahida and M.P. Patel, Arab. J. Chem., 9, 430 (2016); https://doi.org/10.1016/j.arabjc.2014.05.016.
N. Gopal, M. Asaithambi, P. Sivakumar and V. Sivakumar, Indian J. Chem. Technol., 23, 53 (2016).
V.V. Panic, S.I. Seslija, A.R. Nesic and S.J. Velièkovic, Hem. Ind., 67, 881 (2013); https://doi.org/10.2298/HEMIND121203020P.
A. Afkhami and R. Moosavi, J. Hazard. Mater., 174, 398 (2010); https://doi.org/10.1016/j.jhazmat.2009.09.066.
A. Galal Ibrahim, Am. J. Appl. Chem., 4, 221 (2016); https://doi.org/10.11648/j.ajac.20160406.12.
N.M. Mahmoodi, R. Salehi, M. Arami and H. Bahrami, Desalination, 267, 64 (2011); https://doi.org/10.1016/j.desal.2010.09.007.
M. Nitsae, A. Madjid, L. Hakim and A. Sabarudin, Chem. Chem. Technol., 10, 105 (2016).
E. Karadag, F. Topaç, S. Kundakci and Ö.B. Üzüm, Bull. Mater. Sci., 37, 1637 (2014); https://doi.org/10.1007/s12034-014-0723-9.
E. Passaglia, M. Bertoldo, S. Coiai, S. Augier, S. Savi and F. Ciardelli, Polym. Adv. Technol., 19, 560 (2008); https://doi.org/10.1002/pat.1107.
A. Ahmad, S.H. Mohd-Setapar, C.S. Chuong, A. Khatoon, W.A. Wani, R. Kumar and M. Rafatullah, RSC Adv., 5, 30801 (2015); https://doi.org/10.1039/C4RA16959J.
L. Largitte and R. Pasquier, Chem. Eng. Res. Des., 109, 495 (2016); https://doi.org/10.1016/j.cherd.2016.02.006.
N. Ertugay and F.N. Acar, Arab. J. Chem., 10, S1158 (2017); https://doi.org/10.1016/j.arabjc.2013.02.009.