The Malaysian Journal of Analytical Sciences, Vol 12 No 2 (2008): 310 - 321
Sorption
of arsenate by stannum(IV)-EXCHANGED
zeolite
P
Md Jelas Haron*, Ooi Poh
Siang and Anuar Kassim
Chemistry
Department, Faculty of Science
Universiti
Putra Malaysia, 43400 Serdang, Selangor
*Corresponding
author: mdjelas@fsas.upm.edu.my
Abstract
Zeolites are crystalline,
hydrated aluminosilicate containing exchangeable alkaline and alkaline earth
cations in their structural frameworks.
Previous studies have shown
that modification of zeolites
with an active metal cations yield sorbents
with a strong affinity for certain anions.
Recently hydrous tin oxide was found effective to remove arsenic anions
from aqueous solution. In this
study, sodium ion of zeolite P was exchanged with stannum(IV) and used
for sorption of arsenate (As(V)) ion.
Among parameters investigated were effect of pH, As(V) initial
concentrations, contact time, temperature and effect of foreign ions. The results show that As(V) sorption by
stannum(IV) exchanged zeolite P (SnZP) was maximum at about pH 2. The sorption capacities increase with
increasing initial As(V) concentrations and follows Langmuir model with maximum
sorption capacity of 83.33 mg/g at 25°C.
The sorption capacity of As(V) by SnZP increased as temperature
increases from 25 to 70°C showing that the process is endothermic with DH° value of 83.84 kJ mol-1. The free energy change (DG°) for the sorption was
negative showing that the sorption of As(V) ions is spontaneous. The kinetics study shows that the As(V)
sorption follows second order kinetic model.
The free energy (E) was 12.91 kJ mol-1 which shows the
sorption is an ion-exchange process. The
As(V) sorption by SnZP was not affected by the presence sulphate, chloride,
nitrate and carbonate but was significantly reduced by phosphate.
Keywords: Stannum-exchanged zeolit P, arsenic removal,
kinetic, thermodynamic.
References
1. G. T. Spiro and W. M.
Stigliani. 2003. “Chemistry of the Environment”, Prentice-Hall, New Jersey, Part III, p.p. 191-252.
2. D. J. Vaughan. 2006. Elements, 2, 71-75.
3. C. Huang, Jill R Pan,
Maosung Lee and Shihming Yen. 2007. Treatment
of high-level arsenic-containing wastewater by fluidized bed crystallization
process, J Chem Technol
Biotechnol 82:289–294.
4. D. Mohan, and C. U. Pittman
Jr. 2007. J. Hazard. Mater., 142, 1-53.
5. B. Manna, and U. C. Ghosh. 2006. J.
Hazard. Mater., imprint.
6. Yan-hua Xu, Tsunenori Nakajima, Akira Ohki. 2002. Adsorption and removal of arsenic(V) from drinking
water by aluminum-loaded Shirasu-zeolite, Journal of Hazardous Materials B92,
275–287.
7. M. J. Haron, et al. 2007.
J.
Ion Exchange, inprint
8. N. Unlu, and M. Ersoz.
2007. Separation and Purification Technology, 52, 461-469.
9. M. Ozacar, and Y. A.
Sengil. 2003. J. Hazard. Mater., B 98, 211-224.
10. M. Docgan, M. Alkan, A. Turkyylmaz, and Y. Ozdemir. 2004. J.
Hazard. Mater., B 109, 141-148.
11. G. Kantipuly, S. Katragadda,
A. Chow, and H. D. Gesser. 1990. Talanta, 37, 491-517.
12. W. J. Weber and J. C. Morris.
1962. “Advances in Water Pollution Research”, Pergamon Press, N.Y., pp.
231–266.
13. C. K. Jain, and K. Sharma.
2002. Water Air Soil Pollut., 137,
1-19.
14. D. Ozkan, M. Alkan, and M.
Docgan. 2002. Sorption, 8, 341-349.
15. D. Zhao, A. K. SenGupta, and
Y. Zhu. 1995. Ind. Eng.Chem. Res., 34, 2676-2684.
16. Md
Jelas Haron, Farha Ab Rahim, Abdul Halim Abdullah and Mohd Zobir Hussein, Sorption removal of arsenic by
cerium-exchanged zeolite, To be published
17. Md
Jelas Haron*, Saiful Adli Masdan, Mohd Zobir Hussein, Zulkarnain Zainal and Anuar Kassim, Kinetics and Thermodynamic for Sorption of Arsenate by Lanthanum-exchanged Zeolite, Malaysian
J. Analytical Sciences, 11(1) (imprint)
18. J.
Hlavay, K. Polyak. 2005. Determination
of surface properties of iron hydroxide-coated alumina adsorbent prepared for
removal of arsenic from drinking water, J. Colloid Interf. Sci. 284 (1), 71–77.
19. Yu Zhang, Min Yang and Xia
Huang. 2003. Arsenic(V) removal with a
Ce(IV)-doped iron oxide adsorbent Chemosphere 51, 945–952
20. A.
Kilislioglu, and B. Bilgin. 2003. Appl. Radiat. Isotopes, 50, 155-160.