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Densities, Ultrasonic Velocities, Viscosities, and FT-IR Spectra of Binary Mixtures of Morpholine in Isobutyl Acetate, Formamide, and 2-Butanol

  • PHYSICAL CHEMISTRY OF SOLUTIONS
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Abstract

The densities, ultrasonic velocities and viscosities of binary mixtures of morpholine along isobutyl acetate, formamide, and 2-butanol have gone determined at various temperatures over the entire composition range. From the observation data the values of deviation viscosity, excess isentropic compressibility’s (\(\kappa _{s}^{E}\)), and excess thermodynamic properties of the mixture were measured at an absolute dilution. Finally, the theory of Prigogine–Flory–Patterson (PFP) is correlated to recognize most prevalent interactions among the molecules. The Jouyban Acree version was used-up to coordinate the laboratory values of density (ρ), speed of sound, and viscosity (η). Further binary mixing and FT-IR spectra were studied at equimolar concentration have been estimated. The observations were analyzed and explained in terms of molecular package and type of interactions through the formation of hydrogen bonding.

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REFERENCES

  1. V. K. Syal, B. S. Patial, and S. Chauhan, Indian J. Pure Appl. Phys. 37, 366 (1999).

    CAS  Google Scholar 

  2. S. L. Oswal and H. S. Desai, Fluid Phase Equilib. 148, 359 (1998).

    Article  Google Scholar 

  3. C. Pettenati, P. Alessi, M. Fermegila, and I. Kikic, Thermochim. Acta 162, 203 (1990).

    Article  CAS  Google Scholar 

  4. M. Akl Awwad, J. Chem. Eng. Data 53, 307 (2008).

    Article  Google Scholar 

  5. G. V. Rama Rao, A. Viswanath, and G. Rambabu, Indian J. Pure Appl. Phys. 42, 820 (2004).

    Google Scholar 

  6. A. Rose Venis, and X. Rosario Rajkumar, Asian J. Chem. 26, 4711 (2014).

    Article  Google Scholar 

  7. M. Madhuresh and S. Sharma, J. Mol. Liq. 222, 535 (2016).

    Article  Google Scholar 

  8. M. V. Rathnam, S. Mohite, and M. S. S. Kumar, J. Solution Chem. 40, 390 (2011).

    Article  CAS  Google Scholar 

  9. J. A. Riddick, W. B. Bunger, and T. K. Sakano, Organic Solvents, Physical Properties, and Methods of Purifications (Wiley-Interscience, New York, 1986), Vol. 2.

    Google Scholar 

  10. Y. He, R. Jiang, F. Zhu, T. Luan, Zh. Huang, and G. F. Ouyang, J. Chem. Eng. Data 53, 1186 (2008).

    Article  CAS  Google Scholar 

  11. P. Paul Divakar and K. Samatha, Int. Lett. Chem. Phys. Astron. 42, 13 (2015).

    Article  Google Scholar 

  12. A. K. Nain, T. Srivastava, J. D. Pandey, and S. Gopal, J. Mol. Liq. 149, 9 (2009).

    Article  CAS  Google Scholar 

  13. G. Micael, A. Gustavo Bravo-Sanchez, A. E. Iglesias-Silva, and K. R. Baltazar, J. Chem. Eng. Data 55, 2310 (2010).

    Article  Google Scholar 

  14. A. Awasthi and A. Awasthi, Thermochem. Acta 537, 57 (2012).

    Article  CAS  Google Scholar 

  15. V. K. Sharma and R. Dua, J. Chem. Thermodyn. 71, 182 (2014).

    Article  CAS  Google Scholar 

  16. M. A. Saleh and M. H. Uddin, Phys. Chem. Liq. 37, 701 (1999).

    Article  CAS  Google Scholar 

  17. A. M. Cases, A. C. Gómez Marigliano, C. M. Bonatti, and H. N. Sólimo, J. Chem. Eng. Data 46, 712 (2001).

    Article  CAS  Google Scholar 

  18. R. Singh, M. Yasmin, H. Agarwal, V. K. Shukla, M. Gupta, and J. P. Shukla, Phys. Chem. Liq. 51, 606 (2013).

    Article  CAS  Google Scholar 

  19. P. Venkateswara Rao, M. Gowrisankar, L. Venkatramana, T. Srinivasa Krishna, and K. Ravindhranath, J. Chem. Thermodyn. 101, 92 (2016).

    Article  CAS  Google Scholar 

  20. R. J. Fort and W. R. Moore, Trans. Faraday Soc. 61, 2102 (1965).

    Article  CAS  Google Scholar 

  21. A. Ali and A. K. Nain, Pramana J. Phys. 58, 695 (2002).

    CAS  Google Scholar 

  22. V. Mutalik, L. S. Manjeshwar, M. Sairam, and T. M. Aminabhavi, J. Chem. Thermodyn. 38, 1620 (2006).

    Article  CAS  Google Scholar 

  23. B. B. Gurung and M. N. Roy, J. Solution Chem. 35, 1587 (2006).

    Article  CAS  Google Scholar 

  24. O. Redlich and A. T. Kister, J. Ind. Eng. Chem. 40, 341 (1948).

    Article  CAS  Google Scholar 

  25. M. R. Islam and S. K. Quadri, Thermochim. Acta 115, 335 (1987).

    Article  CAS  Google Scholar 

  26. P. J. Flory, R. A. Orwoll, and A. Vrij, J. Am. Chem. Soc. 86, 3515 (1964).

    Article  CAS  Google Scholar 

  27. I. Prigogine, A. Bellemans, and V. Mathot, The Molecular Theory of Solutions (North-Holland, Amsterdam, 1957).

    Google Scholar 

  28. R. A. Orwoll and P. J. Flory, J. Am. Chem. Soc. 89, 6814 (1967).

    Article  CAS  Google Scholar 

  29. M. Costas and D. Patterson, J. Soln. Chem. 11, 807 (1982).

    CAS  Google Scholar 

  30. A. Jouyban, M. Khoubnasabjafari, Z. Vaez-gharamaleki, Z. Fekari, and J. W. Acree, J. Chem. Pharm. Bull. 53, 519 (2005).

    Article  CAS  Google Scholar 

  31. A. Jouyban, A. Fathi-Azarbayjani, M. Khoubnasabjafari, and J. W. E. Acree, Indian J. Chem. A 44, 1153 (2005).

    Google Scholar 

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Correspondence to R. Ramesh Raju.

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Rajani, C., Gowrisankar, M., Kalyani, K. et al. Densities, Ultrasonic Velocities, Viscosities, and FT-IR Spectra of Binary Mixtures of Morpholine in Isobutyl Acetate, Formamide, and 2-Butanol. Russ. J. Phys. Chem. 97, 3028–3036 (2023). https://doi.org/10.1134/S0036024423130174

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