Browse > Article
http://dx.doi.org/10.4491/eer.2009.14.3.164

Phosphate Removal from Aqueous Solution by Aluminum (Hydr)oxide-coated Sand  

Han, Yong-Un (Environmental Biocolloid Engineering Laboratory, Seoul National University)
Park, Seong-Jik (Environmental Biocolloid Engineering Laboratory, Seoul National University)
Park, Jeong-Ann (Environmental Biocolloid Engineering Laboratory, Seoul National University)
Choi, Nag-Choul (Environmental Biocolloid Engineering Laboratory, Seoul National University)
Kim, Song-Bae (Department of Rural Systems Engineering/Research Institute for Agriculture and Life Sciences, Seoul National University)
Publication Information
Environmental Engineering Research / v.14, no.3, 2009 , pp. 164-169 More about this Journal
Abstract
A powder form of aluminum (hydr)oxides is not suitable in wastewater treatment/filtration systems because of low hydraulic conductivity and large sludge production. In this study, aluminum (hydr)oxide-coated sand (AOCS) was used to remove phosphate from aqueous solution. The properties of AOCS were analyzed using a scanning electron microscopy (SEM) combined with an energy dispersive X-ray spectrometer (EDS) and an X-ray diffractometer (XRD). Kinetic batch, equilibrium batch, and closed-loop column experiments were performed to examine the adsorption of phosphate to AOCS. The XRD pattern indicated that the powder form of aluminum (hydr)oxides coated on AOCS was similar to a low crystalline boehmite. Kinetic batch experiments demonstrated that P adsorption to AOCS reached equilibrium after 24 h of reaction time. The kinetic sorption data were described well by the pseudo second-order kinetic sorption model, which determined the amount of P adsorbed at equilibrium ($q_e$ = 0.118 mg/g) and the pseudo second-order velocity constant (k = 0.0036 g/mg/h) at initial P concentration of 25 mg/L. The equilibrium batch data were fitted well to the Freundlich isotherm model, which quantified the distribution coefficient ($K_F$ = 0.083 L/g), and the Freundlich constant (1/n = 0.339). The closed-loop column experiments showed that the phosphate removal percent decreased from 89.1 to 41.9% with increasing initial pH from 4.82 to 9.53. The adsorption capacity determined from the closed-loop experiment was 0.239 mg/g at initial pH 7.0, which is about two times greater than that ($q_e$ = 0.118 mg/g) from the kinetic batch experiment at the same condition.
Keywords
Aluminum-coated sand; Phosphate removal; Sorption; Batch experiment; Closed-loop column experiment;
Citations & Related Records
연도 인용수 순위
  • Reference
1 Rajan, S. S. S., “Adsorption of divalent phosphate on hydrous aluminum oxide,” Nature, 253, 434-436 (1975).   DOI
2 Boujelben, N., Bouzid, J., Elouear, Z., Feki, M., Jamoussi, F., and Montiel, A., “Phosphorus removal from aqueous solution using iron coated natural and engineered sorbents,” J. Hazard. Mater., 151, 103-110 (2008).   DOI   ScienceOn
3 Altundoğan, H. S. and Tümen, F., “Removal of phosphates from aqueous solutions by using bauxite II: The activation study,” J. Chem. Technol. Biotechnol., 78, 824-833 (2003).   DOI   ScienceOn
4 Xiaofang, Y., Zhonxi, S., Dongsheng, W., and Forsling, W., “Surface acid-base properties and hydration/dehydration mechanisms of aluminum (hydr)oxides,” J. Colloid Interf. Sci., 308, 395-404 (2007).   DOI   ScienceOn
5 Edwards, M. and Benjamin, M., “Adsorptive filtration using coated sand: A new approach for treatment of metal-bearing wastes,” J. Water Pollut. Control Fed., 61, 1523-1533 (1989).
6 Fein, J. B., Boily, J. F., Güçlü, K., and Kaulbach, E., “Experimentalstudy of humic acid adsorption onto bacteria and Al-oxide mineral surfaces,” Chem. Geol., 162, 33-45 (1999).   DOI   ScienceOn
7 Blaney, L. M., Cinar, S., and Sengupta, A. K., “Hybrid anion exchanger for trace phosphate removal from water and wastewater,” Water Res., 41, 1603-1613 (2007).   DOI   ScienceOn
8 Lookman, R., Grobet, P., Merckx, R., and Vlassak, K., “Phosphate sorption by synthetic amorphous aluminum hydroxides: A $A^{27}^ Al and^{31}^ $ P solid-state MAS NMR spectroscopy study,” European J. Soil Sci., 45, 37-44 (1994).   DOI   ScienceOn
9 Kim, Y. and Kirkpatrick, R. J., “An investigation of phosphate adsorbed on aluminum oxyhydroxide and oxide phases by nuclear magnetic esonance,” European J. Soil Sci., 55, 243-251 (2004).   DOI   ScienceOn
10 Arias, M., Da Silva-Carballal, J., Carcía-Río, L., Mejuto, J., and Núñez, A., “Retention of phosphorus by iron and aluminum- oxides-coated quartz particles,” J. Colloid Interf. Sci., 295, 65-70 (2006).   DOI   ScienceOn
11 Guan, X. H., Shang, C. S., and Chen, G. H., “Competitive adsorption of organic matter with phosphate on aluminum hydroxide,” J. Colloid Interf. Sci., 296, 51-58 (2006).   DOI   ScienceOn
12 Ayoub, G. M., Koopman, B., and Pandya, N., “Iron and aluminum hydroxy(oxide) coated filter media for low-concentration phosphorus removal,” Water Environ. Res., 73, 478-485 (2001).   DOI   ScienceOn
13 Xu, Y. H., Ohki, A., and Maeda, S., “Removal of arsenate, phosphate, and fluoride ions by aluminum-loaded shirasuzeolite,” Toxicol. Environ. Chem., 76, 111-124 (2000).   DOI   ScienceOn
14 Galarneau, E. and Gehr, R., “Phosphorus removal from wastewaters: Experimental and theoretical support for alternative mechanisms,” Water Res., 31, 328-338 (1997).   DOI   ScienceOn
15 APHA(American Public Health Association), Standard Methods for the Examination of Water and Wastewater, Washington, DC. (1995).
16 Tanada, S., Kabayama, M., Kawasaki, N., Sakiyama, T., Nakamura, T., Araki, M., and Tamura, T., “Removal of phosphate by aluminum oxide hydroxide,” J. Colloid Interf. Sci., 257, 135-140 (2003).   DOI   ScienceOn
17 Guan, X. H., Liu, Q., Chen, G. H., and Shang, C., “Surface complexation of condensed phosphate to aluminum hydroxide: An ATR-FTIR spectroscopic investigation,” J. Colloid Interf. Sci., 289, 319-327 (2005).   DOI   ScienceOn
18 Vaishya, R. C. and Gupta, S. K., “Coated sand filtration: An emerging technology for water treatment,” J. Water Supply, 52, 299-306 (2003).
19 Mathialagan, T. and Viraraghavan, T., “Adsorption of cadmium from aqueous solutions by vermiculite,” Sep. Sci. Technol., 38, 57-76 (2003).   DOI   ScienceOn
20 Ho, Y. S. and Mckay, G., “Pseudo-second order model for sorption processes,” Process Biochem., 34, 451-465 (1999).   DOI   ScienceOn
21 Borggaard, O. K., Raben-Lange, B., Gimsing, A. L., and Strobel, B. W., “Influence of humic substances on phosphate adsorption by aluminum and iron oxides,” Geoderma, 127, 270-279 (2005).   DOI   ScienceOn
22 Genz, A., Kornműller, A., and Jekel, M., “Advanced phosphorus removal from membrane filtrates by adsorption on activated aluminum oxide and granulated ferric hydroxide,” Water Res., 38, 3523-3530 (2004).   DOI   ScienceOn
23 Shin, E. W., Han, J. S., Jang, M., Min, S. H., Park, J. K., and Rowell, R. M., “Phosphate adsorption on aluminum-impregnated mesoporous silicates: Surface structure and behavior of adsorbents,” Environ. Sci. Technol., 38, 912-917 (2004).   DOI   ScienceOn
24 Johnson, B. B., Ivanov, A. V., Antzutkin, O. N., and Forsling, W., $P^{31}^$ nuclear magnetic resonance study of the adsorption of phosphate and phenyl phosphates on γ-$Al_{2}_$ $O_{3}_$ Langmuir, 18, 1104-1111 (2002).   DOI   ScienceOn
25 Altundoğan, H. S. and Tűmen, F., “Removal of phosphate from aqueous solutions by using bauxite.Ⅰ: Effect of pH on the adsorption of various phosphates,” J. Chem. Technol. Biotechnol., 77, 77-85 (2001).   DOI   ScienceOn
26 Kabayama, M., Sakiyama, T., Kawasaki, N., Nakamura, T., Araki, M., and Tanada, S., “Characteristics of phosphate ion adsorption-desorption onto aluminum oxide hydroxide for preventing eutrophication,” J. Chem. Eng. Japan, 36, 499-505 (2003).   DOI   ScienceOn