Please use this identifier to cite or link to this item: https://hdl.handle.net/11147/4103
Title: Synthesis of aminopropyl triethoxysilane-functionalized silica and its application in speciation studies of vanadium(IV) and vanadium(V)
Authors: Erdem, Aslı
Shahwan, Talal
Çağır, Ali
Eroğlu, Ahmet Emin
Keywords: Vanadium(IV)
Vanadium(V)
Amine-functionalized silica
Speciation
Inductively coupled plasma mass spectrometry
Issue Date: 15-Oct-2011
Publisher: Elsevier Ltd.
Source: Erdem, A., Shahwan, T., Çağır, A., & Eroğlu, Ahmet E. (2011). Synthesis of aminopropyl triethoxysilane-functionalized silica and its application in speciation studies of vanadium(IV) and vanadium(V). Chemical Engineering Journal, 174(1), 76–85. doi:10.1016/j.cej.2011.08.049
Abstract: A solid phase extraction sorbent, aminopropyl triethoxysilane-functionalized silica was prepared and used for vanadium speciation prior to inductively coupled plasma mass spectrometric determination. The necessary sorption parameters such as sorption pH, reaction temperature, sorbent amount and sample volume were optimized. The sorption for V(V) and V(IV) under the optimized conditions was 98% (±1) and was lower than 10%, respectively. The sorption process was investigated both from a kinetic perspective and also in terms of Freundlich, Dubinin-Radushkevich and Langmuir isotherm models to characterize the uptake of vanadate ion by the functionalized silica. Desorption from the sorbent was realized with 0.5 mol L−1 thiourea prepared in 0.2 mol L−1 HCl. Among the possible interfering species tested, Te(IV), Se(IV), Se(VI) and Fe(III) showed interference effects with V(V) signal. The validity of the method was first checked via spike recovery experiments with four different types of water; namely ultra pure, bottled drinking, tap, and sea water for different concentrations of V(V). The percent recovery values changed between 87 and 108 for all water types. The accuracy of the proposed methodology was also checked by analyzing a standard reference material (NIST, SRM 1643e) and a good agreement was found between the determined and the certified value. The proposed methodology has also been shown to be applicable for the separate sorption of V(V) in the absence/presence of V(IV) and for the sorption of both V(IV) and V(V) in waters. The amount of V(IV) can then be determined from the difference.
URI: http://doi.org/10.1016/j.cej.2011.08.049
http://hdl.handle.net/11147/4103
ISSN: 1385-8947
1385-8947
1873-3212
Appears in Collections:Chemistry / Kimya
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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