Copyright (c) 2014 AJC
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Removal of Phosphate by Paper Mill Sludge: Adsorption Isotherm and Kinetic Study
Corresponding Author(s) : Sharifah Mohamad
Asian Journal of Chemistry,
Vol. 26 No. 12 (2014): Vol 26 Issue 12
Abstract
Phosphate ions have been removed from aqueous solution by paper mill sludge. The influences of experimental conditions such as pH, amount of adsorbent, initial concentration of phosphate, adsorption isotherm and adsorption kinetics of paper mill sludge were studied. The adsorption of phosphate was more efficient in the basic pH region (pH 12). Pseudo second-order model fits better than the pseudo first-order model for adsorption kinetic data and indicates the adsorption process is based on chemisorptions. The calculated activation energy (Ea) is 37.01 J/mol which further suggests that the sorption of phosphate by paper mill sludge was based on chemical adsorption. Consequently, the equilibrium isotherm data were fitted well to Langmuir isotherm with maximum adsorption capacity of 12.65 mg/g. From the study, it showed that paper mill sludge has the potential to be utilized as a cost effective and high capability adsorbent for removal of phosphate from aqueous solutions.
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T.A. O’Brien, S.J. Herbert and A.V. Barker, Commun. Soil Sci. Plant Anal., 34, 2229 (2003); doi:10.1081/CSS-120024060.
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M. Hojamberdiev, Y. Kameshima, A. Nakajima, K. Okada and Z. Kadirova, J. Hazard. Mater., 151, 710 (2008); doi:10.1016/j.jhazmat.2007.06.058.
K. Karageorgiou, M. Paschalis and G.N. Anastassakis, J. Hazard. Mater., 139, 447 (2007); doi:10.1016/j.jhazmat.2006.02.038.
N.Y. Mezenner and A. Bensmaili, Chem. Eng. J., 147, 87 (2009); doi:10.1016/j.cej.2008.06.024.
N.R. Khalili, J.D. Vyas, W. Weangkaew, S.J. Westfall, S.J. Parulekar and R. Sherwood, Sep. Purif. Technol., 26, 295 (2002); doi:10.1016/S1383-5866(01)00184-8.
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S. Gupta and B.V. Babu, Chem. Eng. J., 150, 352 (2009); doi:10.1016/j.cej.2009.01.013.
Y. Song, H.H. Hahn and E. Hoffmann, Chemosphere, 48, 1029 (2002); doi:10.1016/S0045-6535(02)00183-2.
M.W. Kamiyango, W.R.L. Masamba, S.M.I. Sajidu and E. Fabiano, J. Phys. Chem. Earth, 34, 850 (2009); doi:10.1016/j.pce.2009.07.012.
Y.S. Ho and G. McKay, Trans. I Chem. E, 76B, 332 (1998).
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M.M. Castro López, M.C. Cela Pérez, M.S. Dopico García, J.S. López Vilarino, M.V. González Rodríguez and L.F. Barral Losada, Anal. Chim. Acta, 721, 68 (2012); doi:10.1016/j.aca.2012.01.049.
W.J. Weber Jr. and J.C. Morris, J. Sanit. Eng. Div., 89, 31 (1963).
N. Kannan and M.M. Sundaram, Dyes Pigments, 51, 25 (2001); doi:10.1016/S0143-7208(01)00056-0.
M. Kilic, E. Apaydin-Varol and A.E. Pütün, J. Hazard. Mater., 189, 397 (2011); doi:10.1016/j.jhazmat.2011.02.051.
H. Nollet, M. Roels, P. Lutgen, P. Van der Meeren and W. Verstraete, Chemosphere, 53, 655 (2003); doi:10.1016/S0045-6535(03)00517-4.
I. Langmuir, J. Am. Chem. Soc., 40, 1361 (1918); doi:10.1021/ja02242a004.
G. McKay, H.S. Blair and J.R. Gardner, J. Appl. Polym. Sci., 27, 3043 (1982); doi:10.1002/app.1982.070270827.
M.M. Dubinin and L.V. Radushkevich, Chem. Zent., 1, 875 (1947).
M.J. Temkin and V. Pyzhev, Acta Physiochim. USSR, 12, 217 (1940).
S. Wang, X. Jin, H. Zhao and F. Wu, Aquat. Bot., 89, 23 (2008); doi:10.1016/j.aquabot.2008.01.006.
O.K. Borggaard, B. Raben-Lange, A.L. Gimsing and B.W. Strobel, Geoderma, 127, 270 (2005); doi:10.1016/j.geoderma.2004.12.011.
K. Sakadevan and H.J. Bavor, Water Res., 32, 393 (1998); doi:10.1016/S0043-1354(97)00271-6.
L. Zeng, X. Li and J. Liu, Water Res., 38, 1318 (2004); doi:10.1016/j.watres.2003.12.009.
N. Boujelben, J. Bouzid, Z. Elouear, M. Feki, F. Jamoussi and A. Montiel, J. Hazard. Mater., 151, 103 (2008); doi:10.1016/j.jhazmat.2007.05.057.