Journals / Turkish Journal of Chemistry / 2005 / Cilt: 29 - Sayı: 6

Extraction-Spectrophotometric Determination of Trace Amounts of Barium and Strontium by 18-Crown-6 and Rose Bengal Using Partial Least Squares

Pages
669–678
Publication Date
2005-06-01
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The method was successfully applied to the analysis of spiked water (natural, tap and waste waters) samples.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Partial least squares modeling is a powerful multivariate statistical tool applied to extraction-spectrophotometric simultaneous determination of mixtures of barium and strontium.
📊
Key Findings & Data:The method is based on the formation of the ternary complexes with 18C6 and rose bengal with barium and strontium.
💡
Conclusion & Impact:The method was successfully applied to the analysis of spiked water (natural, tap and waste waters) samples.
🔬Design:Modeling & Simulation
📍Scope:Comprehensive Sample
⚙️Variables:Partial least squares · Extraction-spectrophotometric determination · Barium

Abstract

Partial least squares modeling is a powerful multivariate statistical tool applied to extraction-spectrophotometric simultaneous determination of mixtures of barium and strontium. The method is based on the formation of the ternary complexes with 18C6 and rose bengal with barium and strontium. The 18C6-Ba-RB and 18C6-Sr-RB ternary complexes are quantitatively extracted into dichloromethane and the resolution of the mixtures is accomplished by partial least squares (PLS). In this study, the calibration model is based on absorption spectra in the 500-600 nm range for 25 different mixtures of barium and strontium. Calibration matrice's ranges were 0.05-5.50 and 0.03-4.50 m g mL-1 and detection limits were 0.036 and 0.017 m g mL-1 for barium and strontium, respectively. A series of synthetic solutions containing different concentrations of barium and strontium was used to check the prediction ability of the PLS model. The RMSEP for barium and strontium was 0.1323 and 0.0327, respectively. The method was successfully applied to the analysis of spiked water (natural, tap and waste waters) samples.

Özet

Partial least squares modeling is a powerful multivariate statistical tool applied to extraction-spectrophotometric simultaneous determination of mixtures of barium and strontium. The method is based on the formation of the ternary complexes with 18C6 and rose bengal with barium and strontium. The 18C6-Ba-RB and 18C6-Sr-RB ternary complexes are quantitatively extracted into dichloromethane and the resolution of the mixtures is accomplished by partial least squares (PLS). In this study, the calibration model is based on absorption spectra in the 500-600 nm range for 25 different mixtures of barium and strontium. Calibration matrice's ranges were 0.05-5.50 and 0.03-4.50 m g mL-1 and detection limits were 0.036 and 0.017 m g mL-1 for barium and strontium, respectively. A series of synthetic solutions containing different concentrations of barium and strontium was used to check the prediction ability of the PLS model. The RMSEP for barium and strontium was 0.1323 and 0.0327, respectively. The method was successfully applied to the analysis of spiked water (natural, tap and waste waters) samples.

🔖

Cite This Article

GHASEMI, J. (2005). Extraction-Spectrophotometric Determination of Trace Amounts of Barium and Strontium by 18-Crown-6 and Rose Bengal Using Partial Least Squares. Turkish Journal of Chemistry, Cilt: 29 - Sayı: 6, 669–678. https://ajindex.com/articles/227805

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (30)

  1. R.M. Lzatt, L. Pawlak, J.S. Bradshaw and R.L. Bruening, Chem. Rev. 91, 1721 (1991).
  2. A. Ohki, P.J. Lu and R.A. Barstch, Anal. Chem. 63, 2282 (1994).
  3. K. Suzuki, K. Watanabe, Y. Matsumoto, M. Kobayashi, S. Sato, D. Siswanta and H. Hisamoto, Anal. Chem., 324 (1995).
  4. Y. Takada, Bull. Chem. Soc. Jpn. 52, 2501 (1979).
  5. L.M. Tsay, J.S. Shih and S.C. Wu, Analyst 108, 1108 (1983).
  6. H. Koshima and H. Onishi, Analyst 111, 1261 (1986).
  7. H. Parham and A.G. Fazeli, Anal. Sci. 16, 575 (2000).
  8. K. Nakagawa, S. Okada, Y. Inoue and A. Tai, Anal. Chem. 60, 2527 (1988).
  9. K. Chayama and E. Sekido, Anal. Chim. Acta 248, 511 (1991).
  10. R. Escobar, C. Lamoneda, F. Depablos and A. Guiraum, Analyst 114, 533 (1989). T.C. O’Haver and G.L. Green, Anal. Chem. 48, 312 (1976). T.C. O’Haver, Anal. Chem. 51, 91A (1979).
  11. P. Geladi and B.R. Kowalski, Anal. Chim. Acta 185, 1 (1986). H. Martens and T. Naes, “Multivariate Calibration”, John Wiley, New York, 1991.
  12. A. Lorber, L.E. Wangen and B.R. Kowalski, J. Chemometrics 1, 19 (1987).
  13. R. Marbach and H. M. Heise, Chemometrics Intell. Lab. Syst. 9, 45 (1990).
  14. J.H. Kalivas, J. Chemometrics 13, 111 (1999).
  15. J.H. Kalivas, Chemometrics Intell. Lab. Syst. 45, 215 (1999).
  16. A. Hoskuldsson, J. Chemometrics 2, 211 (1988).
  17. J.H. Kalivas, Anal. Chim. Acta 428, 31 (2001).
  18. J. Ghasemi and A. Niazi, Microchemical J. 68, 1 (2001).
  19. J. Ghasemi, A. Niazi and A. Safavi, Anal. Lett. 34, 1389 (2001).
  20. J. Ghasemi, R. Amini and A. Niazi, Anal. Lett. 35, 533 (2002).
  21. J. Ghasemi and D.E. Mohammadi, Microchemical J. 71, 1 (2002).
  22. J. Ghasemi, A. Niazi and R. Leardi, Talanta 59, 311 (2003).
  23. J. Ghasemi, N. Shahabadi and H.R. Seraji, Anal. Chim. Acta 510, 121 (2004).
  24. J. Ghasemi, S. Saaidpour and A.A. Ensafi, Anal. Chim. Acta 508, 119 (2004).
  25. J. Ghasemi and A. Niazi, Talanta 65, 1168 (2005).
  26. J. Ghasemi and A. Niazi, Anal. Chim. Acta 533, 169 (2005).
  27. M. Otto and W. Wegscheider, Anal. Chem. 61, 1847 (1989). J. Lurie, “Handbook of Analytical Chemistry”, Mir Publishers, Moscow, 1978.
  28. D.M. Haaland and E.V. Thomas, Anal. Chem. 60, 1193 (1988).
  29. K. Wiberg, A. Sterner-Molin and S.P. Jacobsson, Talanta 62, 567 (2004).
  30. P. Naber, H. Elzinga, J. Huffman and J.B. van Zytveld, J. Phys. F:, Met Phys. 12, 981 (1982).