Third Day Poster Session, 17 June 2010 - NanoTR-VI
Third Day Poster Session, 17 June 2010 - NanoTR-VI
Third Day Poster Session, 17 June 2010 - NanoTR-VI
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P<br />
NanoscienceT<br />
<strong>Poster</strong> <strong>Session</strong>, Thursday, <strong>June</strong> <strong>17</strong><br />
Theme F686 - N1123<br />
Determination of Mercury(II) in Water and Wastewater Samples by Cold Vapor Atomic<br />
Absorption Spectrometry After Sepration/Preconcentration with 2-Mercaptobenzothiazole<br />
Immobilized on Alumina-Coated Magnetic Nanoparticles<br />
1<br />
Mohammad Ali KarimiP P, Laleh Sotudehnia KoraniP P, UAsghar Askarpour KabirUP P*<br />
PDepartment of Chemistry &T<br />
1<br />
1<br />
and TNanotechnology Research LaboratoryT (NNRL), Payame Noor University (PNU), Sirjan 78185-<br />
347, Iran<br />
Abstract- In this work first we have synthesized alumina coated magnetite nanoparticles (ACMNPs) and then a simple and new<br />
method has been developed for the separation/preconcentration of trace amounts of mercury ion from aqueous samples for subsequent<br />
measurement by cold vapor atomic absorption spectrometry (CVAAS) based on the adsorption of its 2-mercaptobenzothiazole<br />
complex on modified ACMNPs. The preconcentration factor of the adsorbent at optimum conditions was found as 100. The relative<br />
-1<br />
standard deviation and the detection limit for measurement of Hg(II) in our experiments were less than 2.3% (n =5) and 0.04 ng mLP P,<br />
respectively. The practical applicability of the developed sorbent was examined using water and wastewater samples.<br />
1<br />
Determination of mercury in environmental samples is of<br />
great importance nowadays, because mercury is particularly<br />
toxic element and a widely distributed environmental pollutant<br />
because it is widespread in the lithosphere and in water<br />
Inorganic mercury, especially soluble mercury species, can be<br />
transformed into methyl mercury by the action of<br />
microorganisms and can be accumulated in the tissue of fishes<br />
and birds [1,2]. So, its concentration should be kept under<br />
permanently controlled conditions. We use solid-phase<br />
extraction (SPE) for separation and preconcentration trace<br />
amounts of Hg(II) in different water samples for subsequent<br />
measurement by CVAAS technique [3-5].<br />
In this method, MNPs of FeR3ROR4R were synthesized and then<br />
in alcoholic environment their surface coated with AlR2ROR3R and<br />
sodium dodecyl solfate (SDS). In the after stage a chelating<br />
agent of 2-mercaptobenzothiazol (MBT) for separation this<br />
ionR Rhave been immobilized on modified ACMNPs<br />
(abbreviated as MISACMNPs), as the adsorbent for the<br />
preconcentration of mercury ion from aqueous sample<br />
solutions, has been presented. Then isolated by an adscititious<br />
magnet and the adsorbed Hg ions were eluted with HBr<br />
solution. The MNPs, ACMNPs and MISACMNPs were<br />
characterized by XRD, SEM, TEM and FT-IR spectroscopy.<br />
The influence of various parameters such as acidity, eluting<br />
agents, SDS and MBT concentrations, sample volume, NPs<br />
amounts, interfering ions, time for adsorption and desorption,<br />
etc have been studied and established in details.<br />
In order to check the applicability of the proposed method it<br />
was applied to the seperation/preconcentration and<br />
determination of mercury in water and wastewater samples.<br />
According obtained results, the added mercury ions can be<br />
quantitatively recovered from the water samples by the<br />
proposed procedure. This sorbent was successfully applied for<br />
convenient, fast, simple and efficient enrichment of trace<br />
amounts of mercury ions from environmental water and<br />
wastewater samples.<br />
Easy regeneration is another property of ACMNPs, and the<br />
experiments have proved that these ACMNPs can be reused at<br />
least 3 times on average without the obvious decrease of<br />
recovery after wash/calcine procedures. Furthermore, it avoids<br />
the time-consuming column passing (about 1 h in<br />
conventional SPE method) and filtration operation, and no<br />
clean-up steps were required.<br />
A comparison of the represented method with the other<br />
reported methods showed that the detection limit of the<br />
proposed method is comparable to those in reported methods.<br />
The authors are grateful for the financial support of the<br />
Nanoscience and Nanotechnology Research Laboratory<br />
(NNRL) of Sirjan Payam Noor University for this work.<br />
Figure 1. SEM images of FeR3ROR4 Rnanoparticles (a) and alumina coated<br />
FeR3ROR4 Rnanoparticles (b).<br />
*Corresponding author: a_askar_kabir@yahoo.com<br />
[1] B.C. Mondal, D. Das, A.K. Das, Anal. Chim. Acta 450, 223<br />
(2001).<br />
[2] F.W. Fifield, P.J. Haines, Environmental Analytical Chemistry,<br />
2nd ed (Lackwell Science Ltd, Oxford, UK, 2000).<br />
[3] Q. He, X. Chang, H. Zheng, N. Jiang, and X. Wang, Inter. J.<br />
Environ. Anal. Chem. 88, 373(2008).<br />
[4] C.M.F. Hernandez, A.N. Banza, E. Gock, J. Hazard. Mater. 139,<br />
25 (2007).<br />
[5] E.M. Soliman, M.B. Saleh, S.A. Ahmed, Talanta 69, 55 (2006).<br />
6th Nanoscience and Nanotechnology Conference, zmir, <strong>2010</strong> 809