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Halomethanes in tri-n-octylamine and squalane mixtures at infinite dilution

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Abstract

The retention behavior of eight halomethanes and four saturated hydrocarbons was measured in gas chromatographic stationary phases consisting in tri-n-octylamine (TOA), squalane (SQ) and six TOA+SQ mixtures, at 55.0, 58.5, 62.5 and 65.0°C. Equlibrium constants for complex formation were extracted from experimental data by using a lattice model developed by Martire. The results may be interpreted in terms of the formation of weak hydrogen-bonded complexes, with sociation constants of about 0.13 L-mol−1 for haloforms and 0.07 L-mol−1 for dihalomethanes at 60°C.

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References

  1. D. E. Martire and P. Riedl,J. Phys. Chem. 72, 3478 (1968).

    Google Scholar 

  2. D. F. Cadogan and J. H. Purnell, J. Chem. Soc. A 2133, (1968).

  3. R. J. Laub and R. L. Pecsok,Physicochemical Applications of Gas Chromatography (Wiley, New York, 1978).

    Google Scholar 

  4. J. R. Conder and C. L. Young,Physicochemical Measurements by Gas Chromatography (Wiley, New York, 1979).

    Google Scholar 

  5. E. A. Guggenheim,Trans. Faraday Soc. 56, 1159 (1960).

    Google Scholar 

  6. R. L. Scott,J. Phys. Chem. 75, 3843 (1971).

    Google Scholar 

  7. D. E. Martire,J. Phys. Chem. 87, 2425 (1983).

    Google Scholar 

  8. P. J. Flory,Discuss. Faraday Soc. 49, 7 (1970).

    Google Scholar 

  9. T. J. Bruno, D. E. Martire, M. W. P. Harbison, A. Nicolic, and C. F. Hammer,J. Phys. Chem. 87, 2430 (1983).

    Google Scholar 

  10. R. C. Castells and A. M. Nardillo,J. Soution Chem. 14, 87 (1985).

    Google Scholar 

  11. A. M. Nardillo, R. C. Castells, and E. L. Arancibia,J. Chromatogr. 387, 85 (1987).

    Google Scholar 

  12. J. P. Sheridan, D. E. Martire, and Y. B. Tewari,J. Am. Chem. Soc. 94, 3294 (1972).

    Google Scholar 

  13. J. P. Sheridan, D. E. Martire, and F. P. Banda,J. Am. Chem. Soc. 95, 4788 (1973).

    Google Scholar 

  14. D. E. Martire, J. P. Sheridan, J. W. King, and S. E. O'Donnell,J. Am. Chem. Soc. 98, 3101 (1976).

    Google Scholar 

  15. G. Gee, D. Mangaraj, D. Sims, and G. J. Wilson,Polymer 1, 467 (1960).

    Google Scholar 

  16. R. Philippe, G. Delmas, and M. Couchon,Can. J. Chem. 56, 370 (1978).

    Google Scholar 

  17. R. C. Castells, E. L. Arancibia, and A. M. Nardillo,J. Chromatogr. 504, 45 (1990).

    Google Scholar 

  18. R. R. Dreisbach,Adv. Chem. Ser. 15, (1955);22, (1959);29, (1961).

  19. J. A. Riddick and W. B. Bunger,Organic Solvents, 3rd. edn. (Wiley-Interscience, New York, 1970).

    Google Scholar 

  20. A. Bondi,J. Phys. Chem. 68, 441 (1964).

    Google Scholar 

  21. D. P. Stevenson and G. M. Coppinger,J. Am. Chem Soc. 84, 149 (1962).

    Google Scholar 

  22. C. J. Biaselle and J. G. Miller,J. Am. Chem. Soc. 96, 3813 (1962).

    Google Scholar 

  23. D. W. Marquardt,J. Soc. Appl. Math. 2, 431 (1963).

    Google Scholar 

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Castells, R.C., Arancibia, E.L. & Nardillo, A.M. Halomethanes in tri-n-octylamine and squalane mixtures at infinite dilution. J Solution Chem 22, 85–94 (1993). https://doi.org/10.1007/BF00647057

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