A facile spectrophotometric method for the determination of periodate using azure B

jbchs Journal of the Brazilian Chemical Society J. Braz. Chem. Soc. 0103-5053 1678-4790 Sociedade Brasileira de Química São Paulo, SP, Brazil Foi desenvolvido um método simples, rápido e sensível para a determinação de periodato em amostras de água de rio e em solução. O método é baseado na reação do periodato com iodeto em meio ácido, com liberação de iodo. O iodo liberado diminui a intensidade da cor violeta do azure B, medida em 644 nm. O decaimento da absorbância é diretamente proporcional a concentração de periodato e obedece a lei de Beer na faixa de 0,2 - 5,5 µg mL-1. A absortividade molar, a sensibilidade de Sandell e os limites de detecção e de quantificação encontrados foram 1,09x10(5) L mol-1 cm-1, 1,75x10-3 µg cm-2, 0,07 µg mL-1 and 0,20 µg mL-1, respectivamente. As condições ótimas de reação e os parâmetros analíticos foram avaliados. O efeito de íons interferentes é descrito. O método proposto foi aplicado com sucesso na determinação de periodato em amostras de águas de rio e em solução. ARTICLE A facile spectrophotometric method for the determination of periodate using azure B B. Narayana*; Tom Cherian Department of Post Graduate Studies and Research in Chemistry, Mangalore University, Mangalagangothri – 574 199, India ABSTRACT A simple, rapid and sensitive spectrophotometric method has been developed for the determination of periodate in solution and river water samples. The method is based on the reaction of periodate with iodide in an acid medium to liberate iodine. This liberated iodine bleaches the violet color of the azure B and is measured at 644 nm. This decrease in absorbance is directly proportional to the periodate concentration and obeys Beer's law in the range of 0.2 - 5.5 µg mL-1. The molar absorptivity, Sandell's sensitivity, detection limit and quantitation limit of the method were found to be 1.09 X 105 L mol-1 cm-1 , 1.75 X10-3 µg cm-2, 0.07 µg mL-1 and 0.20 µg mL-1 respectively. The optimum reaction conditions and other analytical parameters were evaluated. The effect of interfering ions on the determination is described. The proposed method has been successfully applied to the determination of periodate in solutions and river water samples. Keywords: periodate determination, spectrophotometry, azure B RESUMO Foi desenvolvido um método simples, rápido e sensível para a determinação de periodato em amostras de água de rio e em solução. O método é baseado na reação do periodato com iodeto em meio ácido, com liberação de iodo. O iodo liberado diminui a intensidade da cor violeta do azure B, medida em 644 nm. O decaimento da absorbância é diretamente proporcional a concentração de periodato e obedece a lei de Beer na faixa de 0,2 – 5,5 µg mL-1. A absortividade molar, a sensibilidade de Sandell e os limites de detecção e de quantificação encontrados foram 1,09x105 L mol-1 cm-1, 1,75x10-3 µg cm-2, 0,07 µg mL-1 and 0,20 µg mL-1, respectivamente. As condições ótimas de reação e os parâmetros analíticos foram avaliados. O efeito de íons interferentes é descrito. O método proposto foi aplicado com sucesso na determinação de periodato em amostras de águas de rio e em solução. Introduction The determination of iodine compounds, particularly periodate, I(VII) is important in organic chemistry, biology and life sciences, but it is rather difficult to determine I(VII) at low concentrations. Periodate is used for the oxidation of different inorganic, organic compounds and catalytic applications at trace levels.1-6 Therefore simple, rapid, sensitive and accurate method is required for the determination of trace amounts of periodate in different samples. Many methods have been reported for the determination of periodate, such as thin layer chromatography,7 capillary zone electrophoresis,8 pulse polarography,9 fluorometry10 Chemeluminiscence.3 Some of the reported chromogenic reagents for the spectrophotometric determination of periodate are 5,5-dimethyl-1,3-cyclohexanedione bisthiosemicarbazone monohydrochloride,11 amodiaquine dihydrochloride,12 ferroin,13 o- dianisidine,14 4- bromo-N,N'- bis ( 2- hydroxypropyl)-o- phenylenediamine,15 2,2'- azinodi (3- ethylbenzothiazol-6-sulphonate).16 Of these reagents, few are reported to be carcinogenic while few others are less selective, less sensitive, time consuming and suffer from small calibration range. The need for a sensitive simple reliable method for the determination of periodate is therefore clearly recognized. In this work a new spectrophotometric method is described for the determination of trace quantities of periodate based on the reaction with azure B. The proposed method is rapid, simple, precise and accurate and is suitable for the determination of periodate in solution and different river water samples. Experimental Apparatus A Secomam Anthelie NUA 002 UV – Visible spectrophotometer with 1 cm quartz cell was used for the absorbance measurements and a WTW pH 330, pH meter was used. Reagents All chemicals used were of analytical reagent or chemically pure grade and double distilled water was used throughout the study. A standard stock solution (1000 µg mL-1) of periodate was prepared by dissolving 0.1205 g of potassium periodate in 100 mL. Hydrochloric acid ( 2 mol L-1), 2% potassium iodide, acetate buffer of pH 4 were used. A 0.05% solution of azure B was prepared by dissolving 0.05 g of azure B (molecular weight = 305.83 ) in 25 mL methanol and made up to 100 mL with distilled water. Procedure Sample solution containing 0.2 - 5.5 µg mL-1 of periodate was transferred into a series of 10 mL calibrated flasks, potassium iodide ( 2% (m/v), 1 mL) then hydrochloric acid ( 2 mol L-1, 1 mL) were added and the reaction mixture was gently shaken until the appearance of yellow color, indicating the liberation of iodine. Azure B ( 0.05%, 0.5 mL ) was then added and the reaction mixture mixture shaken for 2 minutes. The pH of the medium was adjusted by using acetate buffer of pH 4, then the contents were diluted to 10 mL with distilled water and mixed well. The absorbance of the resulting solution was measured at 644 nm against reagent blank. The amount of the periodate present in the volume taken was computed from the calibration graph. Determination of periodate in river water samples An aliquot of the spiked samples containing not more than 5.5 µg mL-1 of the periodate was treated with 1 mL of 2% potassium iodide reagent followed by 1 mL of 2 mol L-1, HCl. The mixture was shaken well until the appearance of yellow color and then 0.5 mL of 0.05% azure B solution was added. The pH of the medium was adjusted by using acetate buffer of pH 4, then the contents were diluted to 10 mL with distilled water and mixed well. The absorbance of the resulting solution was measured at 644 nm against reagent blank . Results and Discussion The absorption spectrum of the azure B ( violet colored species) is presented in Figure 1 and the reaction mechanism is represented in Scheme 1. Effect of iodide concentration and acidity The effect of iodide concentration and acidity on the decolorization was studied with 1 µg mL-1 periodate solution. The oxidation of iodide to iodine was effective in the pH range 1.0 to 1.5, which could be maintained by adding 1 mL of 2 mol L-1 HCl in a final volume of 10 mL . The liberation iodine from KI in an acid medium was quantitative. The appearance of yellow color indicates the liberation of iodine. Although any excess of iodide in the solution will not interfere. It was found that 1- 1.2 mL of 2% KI and 1 mL of 2 mol L-1 HCl were sufficient for the liberation of iodine from iodide by periodate and 0.5 mL of 0.05% azure B was used for subsequent decolorization. Effect of concentration of potassium iodide in reaction system is presented in Figure 2. Effect of pH The variation of absorbance of known concentration of the periodate with pH of the medium was studied. A series of buffer solution differing by pH 1 was prepared, and using each of these buffer, system was studied. The maximum absorbance value was found at pH 4. Hence, the pH was maintained at four throughout the study by using acetate buffer of pH 4. Effect of pH on color intensity is shown in Figure 3. Analytical data The adherence to Beer's law was studied by measuring the absorbance values of solutions varying periodate concentration. A straight line graph was obtained by plotting absorbance against concentration of periodate. Beer's law obeyed in the range of 0.2-5.5 µg mL-1 of periodate. The molar absorptivity and Sandell's sensitivity for colored system was found to be 1.09 ´105 L mol-1 cm-1 , 1.75 ´ 10-3 µg cm-2 respectively. The detection limit (DL = 3.3 s/ S) and quantitation limit (QL= 10 s/ S) [where s is the standard deviation of the reagent blank ( n = 5 ) and S is the slope of the calibration curve] for the periodate determination were found to be 0.07 µg mL-1 and 0.20 µg mL-1 respectively. Ringbom's plot for the periodate determination is shown in Figure 2. Effect of interfering ions The effect of various ions at µg mL-1 levels on the determination of periodate was examined. The tolerance limits of interfering species were established at those concentrations that do not cause more than ± 2% error in absorbance values of periodate at 2 µg mL-1 (Table 1). The results indicated that Cu(II), Fe(III), Ce(IV), Se(IV) and iodate were found to interfere. However, the tolerance level for these ions may be increased by the addition of 1 mL of 1% EDTA. Application The proposed method was applied to the quantitative determination of periodate in solution and various river water samples, the results are presented in Table 2 and 3 respectively. Statistical analysis of the results by t- and F-tests showed no significant difference in accuracy and precision of the proposed and reference method.17 The precision of the proposed method was evaluated by replicate analysis of samples containing periodate at three different concentrations. Conclusions For the first time, azure B has been used as a chromogenic reagent for the spectrophotometric determination of periodate. The proposed method, which is simple and rapid, offers the advantages of sensitivity and wide range of determinations with out the need for extraction or heating. The method does not involve any stringent reaction conditions. The proposed method has been successfully applied to the determination of periodate in solution and various river water samples. Acknowledgements Authors thank the Microtron Centre of Mangalore University, Mangalore, for the technical help. Received: January 17, 2005 Published on the web: July 27, 2005 * e-mail: [e-mail] 1. Townshend , A.; Burns, D.T.; Talanta 1992, 39, 715. Talanta 1992 715 39 Townshend A. Burns D.T. 2. El- Shahawi, M. S.; Farag, A. B.; Anal. Chim. Acta 1995, 307, 139. Anal. Chim. Acta 1995 139 307 El- Shahawi M. S. Farag A. B. 3. Gaikwad, A.; Silva, M.; Perez- Bendito, D.; Analyst 1994, 119, 1819. Analyst 1994 1819 119 Gaikwad A. Silva M. Perez- Bendito D. 4. Radhakrishnamurthi, P. S.; Panda, H. P.; React. Kinet. Catal. Lett. 1980, 14, 193. React. Kinet. Catal. Lett. 1980 193 14 Radhakrishnamurthi P. S. Panda H. P. 5. Evmiridis, N. P.; Analyst 1987, 112 , 825. Analyst 1987 825 112 Evmiridis N. P. 6. Haree, Z. A. K.; Microchem. J. 1985, 31 , 375. Microchem. J. 1985 375 31 Haree Z. A. K. 7. Mohamed, A.; Tiwari, S.; J. Planar. Chromatogr. Mod. Tlc. 1991, 4, 485. J. Planar. Chromatogr. Mod. Tlc. 1991 485 4 Mohamed A. Tiwari S. 8. Honda, S.; Suzuki, K.; Kakehi, K.; Anal. Biochem. 1989, 177, 62. Anal. Biochem. 1989 62 177 Honda S. Suzuki K. Kakehi K. 9. Elmosalamy, M. A. F.; Moody, G. J.; Thomas, J. D. R.; Hassan, S. S. M.; Anal. Lett. 1987, 20, 1541. Anal. Lett. 1987 1541 20 Elmosalamy M. A. F. Moody G. J. Thomas J. D. R. Hassan S. S. M. 10. Jie, N.; Yang, D.; Zhang, Q.; Yang, J.; Song, Z.; Anal. Chim. Acta 1998, 359, 87. Anal. Chim. Acta 1998 87 359 Jie N. Yang D. Zhang Q. Yang J. Song Z. 11. Mochnon, M. C.; Munoz Leyva, J. A.; Anal. Chim. Acta 1982, 140, 2271. Anal. Chim. Acta 1982 2271 140 Mochnon M. C. Munoz Leyva J. A. 12. Verma, K. K.; Gupta, D.; Sanghi, S. K.; Arcana, J.; Analyst 1987, 112, 1519. Analyst 1987 1519 112 Verma K. K. Gupta D. Sanghi S. K. Arcana J. 13. Afkhami, A.; Mosaed, F.; Michrochem. J. 2001, 68, 35. Michrochem. J. 2001 35 68 Afkhami A. Mosaed F. 14. Guernet, M.; Bull. Soc. Chim. Fr. 1964, 3, 478. Bull. Soc. Chim. Fr. 1964 478 3 Guernet M. 15. Stefania, P.; Chem. Anal. 1972, 17, 1267. Chem. Anal. 1972 1267 17 Stefania P. 16. Mahuzier, G.; Kirkacharian, B.A.; Harfouche-Obeika, C.; Anal. Chem. 1975, 76, 79. Anal. Chem. 1975 79 76 Mahuzier G. Kirkacharian B.A. Harfouche-Obeika C. 17. Berzas Nevado, J. J.; Gonzalez, P. V.; Analyst 1989, 114, 989. Analyst 1989 989 114 Berzas Nevado J. J. Gonzalez P. V.