Electrochemical Behavior of Ascorbic Acid and Uric Acid in the Presence of Micelles and Their Selective Determination Application

Gao, Z.; Peng, J.; Han, X.

Artykuł - szczegóły

Tytuł artykułu

Electrochemical Behavior of Ascorbic Acid and Uric Acid in the Presence of Micelles and Their Selective Determination Application

Autorzy

Gao Z. , Peng J. , Han X.

Identyfikatory

Warianty tytułu

Języki publikacji

Abstrakty

The electrochemical behavior of ascorbic acid (AA) and uric acid (UA) in both aqueous cetylpyridinium bromide (CPB) and sodium dodecyl benzene sulfonate (SDBS) micellar solutions have been studied by cyclic voltammetry. The oxidation peak potentials shift more negatively, and the peak currents increase in aqueous CPB micellar solutions for AA and UA. However, the oxidation peak potentials shift more positively, and the peak currents decrease in aqueous SDBS micellar solutions for AA and UA. Therefore, CPB can enhance the electrochemical oxidation reaction for AA and UA, and SDBS hinders the electrochemical oxidation reaction. The electrochemical kinetic parameters for AA and UA in both aqueous CPB and SDBS micellar solutions are determined by chronocoulometry (CC) and chronoamperometry (CA). The charge transfer coefficients _ and the electrode reaction rate constants kf for AA and UA are enhanced in aqueous CPB micellar solutions, but reduced in aqueous SDBS micellar solutions. The pulse differential voltammetric behavior for AAand UAare also investigated in this work. The experimental results show that the oxidation peak potentials forAAandUAare separated by 270mVin the presence ofCPB in aqueous PBS (phosphate buffer solution, pH 6.8) solutions. Thus, AA and UA can be selectively determined in aqueous CPB micellar solutions, especially selectively determination of UA in the presence of excess of AA is possible. According to our work, the practical application of the results can be used to determineUAin human urine and serum samples, the determination results are satisfied.

Słowa kluczowe

electrochemical behaviors ascorbic acid uric acid micelles selective determination

Wydawca

Polskie Towarzystwo Chemiczne

Czasopismo

Polish Journal of Chemistry

Rocznik

2007

Tom

Vol. 81, nr 3

Strony

441--454

Opis fizyczny

Bibliogr. 45 poz., rys.

Twórcy

autor

Gao Z.

autor

Peng J.

autor

Han X.

Key Laboratory of Energy Sources and Chemical Engineering, College of Chemistry and Chemical Engineering, Ningxia University, Yinchuan, 750021, P.R. China

Bibliografia

1. Rusling J.F., Acc. Chem. Res., 24, 75 (1991).
2. Kaifer A.E. and Bard A.J., J. Phys. Chem., 89, 4876 (1985).
3. Ouiatela P.A., Diaz A and Kaifer A.E., Langmuir, 4, 663 (1988).
4. Davidovic A., Tabakovic L, Davidovic D. and Duic L., J. Electroanal. Chem., 280, 371 (1990).
5. Wen X.L., Han Z.X., Rieker A. and Liu Z.L., J. Chem. Research (S), 3, 108 (1997).
6. Wen X.L., Han Z.X., Rieker A. and Liu Z.L., J. Chem. Soc. Perkin Trans. II, 2, 905 (1998).
7. Wen X.L., Jia Y.H. and Liu Z.L., Talanta, 50, 1027 (1999).
8. Connors T.F., Rusling J.F. and Owlia A., Anal Chem., 57, 170 (1985).
9. Stadiober M., Kalcher K, Raber G. and Neuhold C., Talanta, 43, 1915 (1996).
10.Tascioglu S., Tetrahedron, 52, 11113 (1996).
11. Kamau G.N., Leipert T., Shukla S.S. and Rusling J.F., J. Electroanal. Chem., 233, 173 (1987).
12. Rusling J.F. and Nassar A.E.F., J. Am. Chem. Soc., 115, 11891 (1993).
13. Sivagnam U. and Palaniandavar M., J. Electroanal. Chem., 410, 43 (1996).
14. Mandal A.B. and Nair B.U., J. Phys. Chem., 95, 9008 (1991).
15. Wipf D.O. and Wightman R.M., Anal. Chem., 60, 2460 (1988).
16. Xu J., Zhou D. and-Chen H., Fresenius J. Anal. Chem., 362, 234 (1998).
17. Surya A., Murthy N. and Sharma J., Electroanal., 9, 726 (1997).
18. Ueda C., Chi-Sing Tse D. and Kuwana T., Anal. Chem., 54, 850 (1982).
19. Pournaghi-Azar M.H. and Razhmi-Nerbin H., J. Electroanal. Chem., 488, 17 (2000).
20. Wang J.G., Wu Z.Y., Tang J.L., Teng R.R. and Wang E.K., Electroanal., 13, 1093 (2001).
21. Yu A.M., Zhang H.L. and Chen H.Y., Electroanal., 9, 788 (1997).
22. Kulys J. and Drungiliene A., Electroanal., 3, 209 (1991).
23. Xie Y.W. and Dong S.J., Electroanal., 6, 119 (1994).
24. Fei J.J., Luo L.M., Hu S.S. and Gao Z.Q., Electroanal., 16, 319 (2004).
25. Roy P.R., Saha M.S., Okajima T. and Ohsaka T., Electroanal., 16, 289 (2004).
26. Ren J.G., Zhang H.X., Ren Q.L., XiaC.K., Wan J. and QinZ.B., J. Electroanal. Chem., 504,59 (2001).
27. Pachla L.A., Reynolds L.D., Wright S. and Kissinger P.T., J. Assoc. Off. Anal. Chem., 70, l (1987).
28. Zen J.M. and Chen P.J., Anal Chem., 69, 5087 (1997).
29. Nakaminami T., Ito S.I., Kuwabata S. and Yoneyama H., Anal. Chem., 71, 1928 (1999).
30. Wang J., Golden T. and Peng T., Anal. Chem., 59, 740 (1987).
31. Roy P.R., Okajima T. and Ohsaka T., J. Electroanal. Chem., 561, 75 (2004).
32. Khoo S.B. and Chen F., Anal Chem., 74, 5734 (2002).
33. Raj C.R. and Ohsaka T., J. Electroanal Chem., 540, 69 (2003).
34. Kumar S.S., Mathiyarasu J., Phani K.L. and Jain Y.K., Electroanal, 17, 2281 (2005).
35. Goyal R.N., Ahmad S. and Rastogi A., Indian J. Chem., 36A, 283 (1996).
36. Peng J. and Gao Z.N., Anal Bioanal Chem., 384, 1525 (2006).
37. Besio G.J., Prudhomme R.K. and Benziger J.B., Langmuir, 4, 140 (1988).
38. Rusling J.F., Stri G.N., Gosser D.K. and Shukla S.S., J. Electroanal Chem., 240, 201 (1988).
39. Abraham J.S., J. Electroanal Chem., 579, 249 (2005).
40. Yao T., Taniguchi Y, Wasa T. and Musha S., Bull. Chem. Soc. Jpn., 51, 2937 (1978).
41. Harrison J.A. and Khan Z.A., J. Electroanal. Chem., 28, 131 (1970).
42. Bockris J.O.M. and Reddy A.K.N., Modern Electrochemistry, 2nd Ed., Plenum Press, NY, (Chapt. 9) (1998).
43. Adams R.N., Electrochemistry at Solid Electrodes. Marcel Dekker, NY, p. 220 (1969).
44. Liu Z.L., Han Z.X., Yu K.C., Zhang Y.L. and Liu Y.C., J. Phys. Org. Chem., 5, 33 (1992).
45. Galus Z., Fundamentals of Electrochemical Analysis, Ellis Horwood, NY, 398 (1994).

Typ dokumentu

Bibliografia

Identyfikator YADDA

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