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http://dx.doi.org/10.3740/MRSK.2017.27.3.166

Sorption Behavior and Mechanism of Phosphate onto Natural Magnesite  

Xie, Fazhi (School of Materials Science and Chemical Engineering, Anhui Jianzhu University)
Hu, Tingting (School of Materials Science and Chemical Engineering, Anhui Jianzhu University)
Oh, Won-Chun (Department of Advanced Materials & Science Engineering, Hanseo University)
Sheng, Dandan (School of Materials Science and Chemical Engineering, Anhui Jianzhu University)
Li, Haibin (School of Materials Science and Chemical Engineering, Anhui Jianzhu University)
Wang, Xuechun (School of Materials Science and Chemical Engineering, Anhui Jianzhu University)
Xie, Zhiyong (School of Materials Science and Chemical Engineering, Anhui Jianzhu University)
Li, Guolian (School of Environment and Energy Engineering, Anhui Jianzhu University)
Han, Xuan (School of Materials Science and Chemical Engineering, Anhui Jianzhu University)
Xie, Wenjie (School of Materials Science and Chemical Engineering, Anhui Jianzhu University)
Sun, Mei (School of Materials Science and Chemical Engineering, Anhui Jianzhu University)
Publication Information
Korean Journal of Materials Research / v.27, no.3, 2017 , pp. 166-171 More about this Journal
Abstract
Removal of phosphate from environmental water has become more important to prevent eutrophication. In the present study, sorption behavior of phosphate onto magnesite was investigated under different conditions. The optimum pH of phosphate adsorption was determined to be 6.0. The adsorption capacity was found to decrease with increasing temperature, which indicates that a low temperature was beneficial for phosphate adsorption. The sorption capacity for phosphate was found to be 10.2 mg/g at an initial concentration of 100 mg/L and a dose of 2 g/L. The first order kinetic equation and Freundlich isotherm model fit the data well. Phosphate adsorption on magnesite was explained by electrostatic attraction and weak physical interactions.
Keywords
magnesite; phosphate; adsorption; eutrophication; mechanism;
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1 L. G. Yan, Y. Y. Xu, H. Q. Yu, X. D. Xin, Q. Wei and B. Du, J. Hazard. Mater., 179, 244 (2010).   DOI
2 I. Kipcak and M. Ozdemir, Chem. Eng. J., 189, 68 (2012).
3 M. Wang, L. Liao, X. Zhang and Z. Li, Appl. Clay Sci., 67, 164 (2012).
4 N. Gence and H. Ozda , Int. J. Miner. Process., 43, 37 (1995).   DOI
5 R. Chitrakar, S. Tezuka, A. Sonoda, K. Sakane, K. Ooi and T. Hirotsu, J. Colloid Interf. Sci., 298, 602 (2006).   DOI
6 A. Gok, M. K. Gok, Y. S. Asci and M. Lalikoglu, Fluid Phase Equilibr., 372, 15 (2014).   DOI
7 K. Y. Foo and B. H. Hameed, Chem. Eng. J., 156, 2 (2010).   DOI
8 C. J. Zhou, Q. L. Wu, T. Z. Lei and L. L. Negulescu, Chem. Eng. J., 251, 17 (2014).   DOI
9 S. Karaca, A. Gurses, M. Ejder and M. Ac ikyildiz, J. Colloid Interf. Sci., 277, 257 (2004).   DOI
10 S. H. Yeom and K. Y. Jung, J. Ind. Eng. Chem., 15, 40 (2009).   DOI
11 B. Li and M. T. Brett, Water Res., 46, 837 (2012).   DOI
12 T. Liu, K. Wu and L. Zeng, J. Hazard. Mater., 217, 29 (2012).
13 B. Saha, S. Chakraborty and G. Das, J. Colloid Interf. Sci., 331, 21 (2009).   DOI
14 J. B. Xiong, Z. L. He, Q. Mahmood, D. Liu, X. Yang and E. Islam, J. Hazard. Mater., 152, 211(2008).   DOI
15 D. S. Soejoko and M. O. Tjia, J. Mater. Sci., 38, 2087 (2003).   DOI