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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

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