Współczesne podejścia elektrochemiczne do oznaczania arsenu

• Autorzy: Ozimek W. , Rutkowska I. A. , Cox J. A. , Kulesza P. J.

Warianty tytułu

EN

Recent approaches to electrochemical determination of arsenic

• Języki publikacji: PL

Abstrakty

EN

There has been growing interest in development of new methods for the determination of arsenic due to its high toxity and increasing population in the environment. At present, chromatographic (separation) and spectroscopic (detection) approaches are the most common. Although, they are characterized by high sensitivity and low detection limits, the experimental procedures often require generation of toxic AsH3. Electrochemical methods for the determination of arsenic can be considered as complimentary because they are fairly simple and they are subject to different selectivity criteria. In this respect, various stripping voltammetric procedures are becoming popular. The actual stripping voltammetric measurement consists of two steps in which preconcentration of an analyte at the electrode surface is followed by the so called „stripping” step involving electrode reaction recorded in a form of the voltammetric peak. A representative approach involves reduction of the analyte anions upon application of the sufficiently negative potential to form As(0) on the electrode (e.g. gold) surface; this step is followed by voltammetric oxidation (anodic stripping) of the deposit (to As(III)). In a case of so called cathodic stripping voltammetry, the stationary Hanging Mercury Drop Electrode (HMDE) is often used. During the preconcentration step, an insoluble salt is produced on the electrode surface. To facilitate its formation, copper or selenium species are used as mediators. Under such conditions, insoluble Cu3As2 is generated together with copper amalgam on the surface of HMDE. Because sensitivity and detection limit in electroanalytical determinations strongly depend on the current densities measured, there is a need to search for specific catalytic materials that would induce otherwise highly slow and irreversible redox processes of As(III) (oxidation) and, in particular, As(V) (reduction). Designing effective electrocatalytic materials would be of importance to the development of more sensitive stripping methods and monitoring of arsenic under chromatographic and flow conditions. Representative examples of catalytic systems are provided and discussed here. Some attention is also paid to application of enzymes to sensing of arsenic. Electrochemical determination of arsenic(III) is generally better described in literature. Direct determination of As(V) typically requires its binding into chemical compounds. It is reasonable to expect intense research in future aiming at the developing of new electroanalytical methods for direct selective determination of As(V).

Słowa kluczowe

PL

arsen; oznaczenia elektrochemiczne; woltamperometria strippingowa; elektrokataliza; elektrody modyfikowane; nanocząstki metali; nanocząstki tlenków metali

EN

arsenic; electrochemical determinations; stripping voltammetry; electrocatalysis; modified electrodes; metal nanoparticles; metal oxide nanoparticles

• Wydawca: Polskie Towarzystwo Chemiczne
• Czasopismo: Wiadomości Chemiczne
• Rocznik: 2015
• Tom: [Z] 69, 9-10
• Strony: 809--822
• Opis fizyczny: Bibliogr. 34 poz.

Twórcy

autor

Ozimek W.

• Wydział Chemii, Uniwersytet Warszawski ul Pasteura 1, 02-093 Warszawa

autor

Rutkowska I. A.

• Wydział Chemii, Uniwersytet Warszawski ul Pasteura 1, 02-093 Warszawa

autor

Cox J. A.

• Department of Chemistry and Biochemistry, Miami University, Oxford, OH 45056, USA

autor

Kulesza P. J.

• Wydział Chemii, Uniwersytet Warszawski ul Pasteura 1, 02-093 Warszawa

Bibliografia

• [1] A. Eaton, H.C. Wang, J. Northington, Analytical Chemistry of Arsenic in Drinking Water, AWWA Research Foundation and American Water Works Association, Denver 1998, str. 2.
• [2] A. Goswami, P.K. Raul, M.K. Purkati, Chem. Eng. Res. Des., 2012, 90, 1387.
• [3] S.B. Rasul, A.K.M. Munir, Z.A. Hossain, A.H. Khan, M. Alauddin, A. Hussam, Talanta, 2002, 58, 33.
• [4] M. Chen, Y. Lin, C. Gu, J. Wang, Talanta, 2013, 104, 53.
• [5] D.E. Mays, A. Hussam, Anal. Chim. Acta, 2009, 646, 6.
• [6] W.W. Kubiak, R. Piech, Skrypt. Akademia Górniczo-Hutnicza, Wydział Inżynierii Materiałowej i Ceramiki, Katedra Chemii Analitycznej.
• [7] R.S. Sadana, Anal. Chem., 1983, 55, 304.
• [8] I.N. Savina, C.J. English, R.L.D. Whitby, Y. Zheng, A. Leistner, S.V. Mikhalovsky, A.B. Cundy, J. Hazard. Mater., 2011, 192, 1002.
• [9] M.M. Ottakama Thotiyl, H. Basti, J. A. Sanchez, C. Goyer, L. Coche-Guerente, P.Dumy, S.Sampath, P. Labbe, J.C. Moutet, J. Colloid Interface Sci. 2012, 383, 130.
• [10] M. Hossani, Md. M. Islam, S. Ferdousi, T. Okajima, T. Ohsaka, Electroanalysis, 2008, 20, 2435.
• [11] J.P. Arnold, R.M. Johnson, Talanta, 1969, 16, 1191.
• [12] S.B. Rasul, A.K.M. Munir, Z.A. Hossani, A.H. Khan, M. Alauddin, A. Hussam, Talanta, 2002, 58, 33.
• [13] E. Punrat, S. Chuanuwatanakul, T. Kaneta, S. Motomizu, O .Chailapakul, Talanta, 2013, 116, 1018.
• [14] N. Moghimi, M. Mohapatra, K.T. Leung, Anal. Chem., 2015, 87, 5546.
• [15] C. Gao, X.-Y. Yu, S.-Q. Xiong, J.-H. Liu, X.-J. Huang, Anal. Chem., 2013, 85, 2673.
• [16] A.Cavicchioli, M.A. La-Scalea, I.G.R. Gutz, (Review) Electroanalysis, 2004, 16, 697.
• [17] C. Locatelli, Electroanalysis, 1997, 9, 1014.
• [18] J. Zima, C.M.G van der Berg, Anal. Chim. Acta, 1994, 289, 291.
• [19] L. Jiajie, Y. Nagosa, Anal. Chim. Acta, 2007, 593, 1.
• [20] U. Greulach, G. Henze, Anal. Chim. Acta, 1995, 306, 217.
• [21] G. Henze, W. Wagner, S. Sander, Fresenius J. Anal. Chem., 1997, 358, 741.
• [22] D. Li, J. Li, X. Jia, Y. Hang, E. Wang, Anal. Chim. Acta, 2012, 733, 23.
• [23] P.J. Kulesza, J. Electroanal. Chem., 1987, 20, 299.
• [24] J.A. Cox, P.J. Kulesza, Anal. Chem., 1984, 56, 1021.
• [25] J.A. Cox, R. Jaworski, P.J. Kulesza, Electroanalysis, 1991, 3,869.
• [26] J.A. Cox, P.J. Kulesza, Catalytic Surfaces for Electroanalysis, Encyclopedia of Analytical Chemistry, R.A. Meyers (Red.), John Wiley, 2009.
• [27] J.A. Cox, B.K. Das, J. Electroanal. Chem., 1987, 233, 87.
• [28] D.V. Ca, L. Sun, J.A. Cox, Electrochim. Acta, 2006, 51, 2188.
• [29] P.J. Kulesza, Analusis, 1988, 16, 125.
• [30] W. Ozimek, Praca magisterska, Wydział Chemii Uniwersytetu Warszawskiego, Warszawa 2014.
• [31] S. Sanllorente-Mendez, O. Dominguez-Renedo, M.J. Arcos-Martinez, Sensors (Basel), 2010, 10, 2119.
• [32] Y. Liu, W. Wei, Electrochem. Commun., 2008, 10, 872.
• [33] D.Q. Hung, O. Nekrassova, R.G. Compton, Talanta, 2004, 64, 269.
• [34] J.T. Van Elteren, Z.Slejkovec, J. Chromatogr. A, 1997, 789, 339.

Uwagi

Praca została opublikowana w specjalnym numerze „Wiadomości Chemicznych”, poświęconym pamięci Profesora Stanisława Głąba, w 70-tą rocznicę Jego urodzin