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Excess Volumetric and Spectroscopic Properties of Mixtures of Some n-Alkoxyethanols and of Some Polyethers with 2-Pyrrolidinone and N-Methyl-2-Pyrrolidinone at 298.15 K

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Abstract

Excess molar volumes VmE for binary liquid mixtures of n-alkoxyethanols or polyethers + 2-pyrrolidinone or N-methyl-2-pyrrolidinone have been measured with a continuous dilution dilatometer at 298.15 K and atmospheric pressure as a function of composition. The alkoxyethanols are diethylene glycol monomethylether, 2-(2-methoxyethoxy) ethanol, CH3(OC2H4)2OH; diethylene glycol monoethylether, 2-(2-ethoxyethoxy) ethanol, C2H5(OC2H4)2OH; and diethylene glycol monobutylether, 2-(2-butoxyethoxy) ethanol, C4H9(OC2H4)2OH; whereas the polyethers are diethylene glycol dimethylether, bis(2-methoxyethyl)ether, CH3(OC2H4)2OCH3; diethylene glycol diethylether, bis(2-ethoxyethyl)ether, C2H5(OC2H4)2OC2H5; and diethylene glycol dibutylether, bis(2-butoxyethyl)ether, C4H9(OC2H4)2OC4H9. In all mixtures the excess molar volumes are negative and symmetric across the entire composition range. The excess volumes are fitted to the Redlich–Kister polynomial equation to obtain the binary coefficients and the standard errors. The experimental results have also been discussed on the basis of IR measurements.

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References

  1. A. Pal and A. Kumar, Indian J. Chem. 43A, 722 (2004).

    Google Scholar 

  2. A. Pal and A. Kumar, J. Indian Chem. Soc. 81, 375 (2004).

    Google Scholar 

  3. A. Pal and A. Kumar, J. Chem. Sci. 116, 39 (2004).

    Google Scholar 

  4. A. Pal and H. Kumar, J. Chem. Thermodyn. 36, 173 (2004).

    Article  Google Scholar 

  5. A. Pal and H. Kumar, Indian J. Chem. 40A, 598 (2001).

    Google Scholar 

  6. A. Pal and H. Kumar, J. Mol. Liquids 94, 163 (2001).

    Article  Google Scholar 

  7. A. Pal, A. Kumar, and H. Kumar, Indian J. Chem. 41A, 2017 (2002).

    Google Scholar 

  8. A. Pal and R. K. Bhardwaj, J. Chem. Eng. Data. 47, 1128 (2002).

    Article  Google Scholar 

  9. A. Pal and S. Sharma, J. Chem. Eng. Data. 43, 532 (1998).

    Article  Google Scholar 

  10. A. Pal and Y. P. Singh, J. Chem. Thermodyn. 26, 1063 (1994).

    Article  Google Scholar 

  11. J. A. Riddick, W. B. Bunger, and T. K. Sakano, Organic Solvents, Physical Properties and Methods of Purification, 4th edn. [Wiley (Interscience), New York, 1986].

    Google Scholar 

  12. R. Francesconi, C. Castellari, and F. Comelli, J. Chem. Eng. Data. 44, 1373 (1999).

    Article  Google Scholar 

  13. J. C. Cobos, Ph.D. Thesis, Universidad de Valladolid, Spain, 1987.

  14. G. Douheret, C. Salgado, M. I. Davis, and J. Loya, Thermochim. Acta. 207, 313 (1992).

    Article  Google Scholar 

  15. L. M. Trejo, M. Costas, and D. Patterson, J. Chem. Soc. Faraday Trans. 87, 3001 (1991).

    Article  Google Scholar 

  16. F. J. Caramona, F. J. Arroyo, G. I. Garcia de la Fuente, J. A. Gonzalez, and J. C. Cobos, Can. J. Chem. 77, 1608 (1997).

    Article  Google Scholar 

  17. A. Serna, I. Garcia de la Fuente, J. A. Gonzalez, and J. C. Cobos, Fluid Phase Equilibr. 133, 187 (1997).

    Article  Google Scholar 

  18. G. Roux, G. Perron, and J. E. Desnoyers, Can. J. Chem. 56, 2808 (1978).

    Google Scholar 

  19. J. A. Riddick and W. B. Bunger, Organic Solvents: Techniques of Chemistry, 3rd edn. [Wiley (Interscience), New York, 1970].

    Google Scholar 

  20. J. George and N.V. Sastry, J. Chem. Eng. Data. 49, 235 (2004).

    Article  Google Scholar 

  21. A. M. A. Al-Mashhadani and A. M. Awwad, Thermochim. Acta. 89, 75 (1985).

    Article  Google Scholar 

  22. E. Dickinson, D. C. Hunt, and I. A. McLure, J. Chem. Thermodyn. 7, 731 (1975).

    Google Scholar 

  23. A. Pal, Y. P. Singh, and W. Singh, Indian J. Chem. 33A, 1083 (1994).

    Google Scholar 

  24. IUPAC (Commission on Atomic Weights and Isotopic Abundances) Pure Appl. Chem. 58, 1677 (1986).

    Google Scholar 

  25. M. G. Prolongo, R. M. Masegosa, H. I. Fuentes, and A. Horta, J. Phys. Chem. 88, 2163 (1984).

    Article  Google Scholar 

  26. J. A. Walmsley, J. Phys. Chem. 82, 2031 (1978).

    Article  Google Scholar 

  27. J. Jadzyn, J. Malecki, and C. Jadzyn, J. Phys. Chem. 82, 2128 (1978).

    Article  Google Scholar 

  28. J. A. Walmsley, E. J. Jacob, and H. B. Thompson, J. Phys. Chem. 80, 2745 (1976).

    Article  Google Scholar 

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Pal, A., Kumar, A. Excess Volumetric and Spectroscopic Properties of Mixtures of Some n-Alkoxyethanols and of Some Polyethers with 2-Pyrrolidinone and N-Methyl-2-Pyrrolidinone at 298.15 K. J Solution Chem 34, 917–927 (2005). https://doi.org/10.1007/s10953-005-6256-5

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  • DOI: https://doi.org/10.1007/s10953-005-6256-5

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