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Modified peak compression sampling in fast micro-HPLC

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Summary

The advantages of short microbore columns packed with a sorbent having a particle diameter of 3µm, such as the speed of analysis, the high solute concentration in the effluent and the detectability of small quantities are experimentally verified. The broadening in the valve is eliminated by the peak compression technique reached by adding a ion-pairing agent into the sample. The examples of catecholamines show the dependence of the height equivalent to a theoretical plate on the velocity of the mobile phase. The optimum is h=3 for a column 30mm long, i.d. 0.7mm, particle diameter 3µm. The minimal detectable quantity with a two-electrode amperometric detector with a gold electrode is from 30 to 40fmol for catecholamines.

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References

  1. F. F. Erni, J. Chromatogr.282, 371 (1983).

    Article  CAS  Google Scholar 

  2. E. Katz, R. P. W. Scott, J. Chromatogr.253, 159 (1982).

    Article  CAS  Google Scholar 

  3. N. Meller, Chromatographia16, 359 (1982).

    Article  Google Scholar 

  4. J. M. Di Bussolo, M. W. Dong, J. R. Gant, J. Liquid Chromatogr.6, 2353 (1983).

    Article  Google Scholar 

  5. H. J. Issaq, R. E. Gourley, J. Liquid Chromatogr.6, 1375 (1983).

    Article  CAS  Google Scholar 

  6. H. J. Issaq, J. Liquid Chromatogr.7, 883 (1984).

    Article  CAS  Google Scholar 

  7. J. F. Reinhard, J. A. Perry, J. Liquid Chromatogr.7, 1211 (1984).

    Article  CAS  Google Scholar 

  8. M. Verzele, J. Chromatogr.295, 81 (1984).

    Article  CAS  Google Scholar 

  9. G. Guiochon, in “High Performance Liquid Chromatography, Advances and Perspectives”, Vol. 2,Cs. Horváth, ed., Academic Press, New York, 1980; p. 36.

    Google Scholar 

  10. T. Takeuchi, D. Ishii, A. Nakanishi, J. Chromatogr.285, 97 (1984).

    Article  CAS  Google Scholar 

  11. K. Jinno, J. High Resolut. Chromatogr./Chromatogr. Commun.7, 66 (1984).

    Article  CAS  Google Scholar 

  12. K. Jinno, J. High Resolut. Chromatogr./Chromatogr. Commun.7, (1984).

  13. M. Krejčí, K. Šlais, D. Kouřilová, Chem. Listy78, 469 (1984).

    Google Scholar 

  14. P. Kucera, J. Chromatogr.198, 93 (1980).

    Article  CAS  Google Scholar 

  15. K. Šlais, D. Kouřilová, Chromatographia16, 265 (1982).

    Article  Google Scholar 

  16. K. Šlais, D. Kouřilová, J. Chromatogr.258, 57 (1983).

    Article  Google Scholar 

  17. D. Kouřilová, K. Šlais, M. Krejčí, Collect. Czech. Chem. Commun.49, 764 (1984).

    Google Scholar 

  18. K. Šlais, D. Kouřilová, M. Krejčí, J. Chromatogr.282, 363 (1983).

    Article  Google Scholar 

  19. J. H. Knox, R. A. Hartvick, J. Chromatogr.204, 3 (1981).

    Article  CAS  Google Scholar 

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Kouřilová, D., Šlais, K. & Krejčí, M. Modified peak compression sampling in fast micro-HPLC. Chromatographia 19, 297–300 (1984). https://doi.org/10.1007/BF02687758

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  • DOI: https://doi.org/10.1007/BF02687758

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