Issue
Korean Journal of Chemical Engineering,
Vol.35, No.7, 1488-1499, 2018
Ultrasonic study on binary liquid mixtures of propiophenone with anilines and alkyl substituted anilines at T=303.15 to 318.15 K
Densities 'ρ', ultrasonic speeds of sound 'u' of binary mixtures of propiophenone (PPH) with aniline, NMethylaniline, N,N-dimethylaniline and N,N-diethylaniline were measured over the entire composition range from 303.15 K to 318.15 K and at atmospheric pressure 0.1MPa. Experimental data of ultrasonic sound were compared and discussed with the computed values of 'u' from various velocity theories like Nomoto's relation (UNOM), impedance relation (UIMP), Van Dael and Vangeel's ideal mix relation (UVDV), Rao's specific velocity relation (URAO), Junjie's theory (UJUN) and Jouyban-Acree's (UJOE) relation for the above binary mixtures over the entire mole fraction range at the studied temperatures. The results are satisfactory and are in agreement between the theoretical and the experimental values. Further, the molecular interaction parameter (α), average percentage error and Chi-square test values were computed by using the values of experimental and theoretical ultrasonic velocities. The Δu values were correlated with Redlich-Kister polynomial equation to compute the coefficients and the standard deviations of the binary mixtures. The results were analyzed in terms of intermolecular interactions.
[References]
  1. Rathnam MV, Bhanushali KR, Sayed RT, Kumar MSS, J. Mol. Liq., 173, 35, 2012
  2. Sahin M, Ayranci E, J. Chem. Thermodyn., 177, 43, 2011
  3. Kannappan V, Xavier JRS, Shanthi RJ, Indian J. Pure. Appl. Phys., 41, 690, 2003
  4. Amalendu, Sureshkumar, J. Ind. Chem. Soc., 81, 101, 2004
  5. Chauhan MS, Kumar A, Chauhan S, Acoust. Lett., 21, 228, 1998
  6. Samatha K, Babu VVH, Sreeramamurthy J, Acustica, 84, 169, 1998
  7. Rita M, Meenakshi, J. Ind. Chem. Soc., 82, 791, 2005
  8. Oswal SL, et al., Thermochim. Acta, 507-508, 27, 2010
  9. Narendra K, Sudhamsa B, Srath BM, J. Chem. Sci., Res. J. Chem. Sci., 4(8), 42, 2014
  10. Investigation of steric effect in the formation of hydrogen-bonded complexes of isomeric chlorophenols with N,N-dimethylaniline; Muhamed RR, Rajesh R, Kannappan V, Arulappan S, Prabaharan A;https://doi.org/10.1016/j.molliq.2017.08.068.
  11. Ultrasonic study of molecular interaction in Binary liquid mixture at 308 K D. Ubagaramary, Dr.Neeraja IOSR J. of Applied Chemistry (IOSR-JAC) ISSN: 2278-5736. 2, Issue 5 (Nov. . Dec. 2012), PP 01-19 www.iosrJ.s.org.
  12. Gowrisankar M, Venkateswarlu P, Sivakumar K, Sivarambabu S, Arabian J. Chem., 10, S2625, 2015
  13. Gowrisankar M, Venkateswarlu, Sivakumar K, Sivarambabu S, J. Solution Chem., 42, 916, 2013
  14. Pandiyan V, Oswal SL, Vasantharani P, Thermochim. Acta, 518(1-2), 36, 2011
  15. Nomato O, J. Phys. Soc., Jan 13, 1528 (1958).
  16. VanDeel and Vangeel E, Proceeding of first international conference on colorimetry thermodynamics, Warsaw (1969) 555.
  17. VanDeel W, Experimental thermodynamics Vol-II Butterworths, London (1975) Chap XI.
  18. Junjie Z, J. China Univ. Sci. Technol., 14, 298, 1984
  19. Schaaffs W, Z. phys 114, 110 (1939).
  20. Schaaffs W, Molekularkustik, Springer, Verlag, Heidelberg (1963) chap XI and XII.
  21. Jouyban A, Khoubnasabjafari M, Vaezgharamaleki Z, Fekari Z, Acree WE, Chem. Pharmaceutical Bulletin, 53, 519, 2005
  22. Bindhani SK, Roy GK, Mohanty YK, Kubendran TR, Russian J. Phys. Chem. A, 89, 1828, 2015
  23. Vasundhara P, Rao CN, Venkatramana L, Kumar KS, Venkateswarlu P, Gardas RL, J. Mol. Liq., 158, 202, 2015
  24. Begum Z, Sandhyasri PB, Rambabu C, ISRN Phys. Chem., Article ID 943429, 12 (2012).
  25. Ramarao GV, Triveni M, Ramachandran D, Int. J. Eng. Res, 3, 2015
  26. Tiwari K, Patra C, Chakravortty V, Acoustics Lett., 19, 53, 1995
  27. Pal A, Kumar A, Indian J. Physics, 78(12), 1319, 2004
  28. Reddy Y, Naidu S, Prasad KR, Indian J. Pure Appl. Phys., 32, 958, 1994
  29. Balakrishnan S, Chem. Sci. Transactions, 4(1), 107, 2015
  30. Babavali SF, Shakira P, Srinivasu C, Narendra K, Karbala International J. Modern Sci., 1, 172, 2015
  31. Redlich O, Kister AT, J. Ind. Eng. Chem., 40, 345, 1948
  32. Alonso I, Alonso V, Mozo I, de la Fuente IG, Gonzalez JA, Cobos JC, J. Chem. Eng. Data, 55(7), 2505, 2010
  33. Su LY, Wang HJ, J. Chem. Thermodyn., 41(3), 315, 2009
  34. Nain AK, Fluid Phase Equilib., 259(2), 218, 2007
  35. Gowrisankar M,Venkateswarlu, Sivakumar K, Sivarambabu S, J. Solution Chem., 42, 916, 2013
  36. Palepu R, Diver J, Campell D, J. Chem. Eng. Data, 30, 355, 1985
  37. Oswal SL, Pandiyan V, Krishnakumar B, Vasantharani, Thermochim. Acta, 507, 27, 2010
  38. Gowrisankar M, Venkateswarlu P, Sivakumar K, Sivarambabu S, J. Mol. Liq., 173, 172, 2012
  39. Korosi G, Kovats ESZ, J. Chem. Eng. Data, 26, 323, 1981
  40. Bindhani SK, Roy GK, Mohanty YK, Kubendran TR, Russian J. Phys. Chem. A, 91, 1037, 2017
  41. Manukonda GS, Venkatalakshami, Rambabu K, Int. J. Phys. Res., 3(4), 5, 2013
  42. Rao VS, Krishna TV, Mohan TM, Rao PM, J. Chem. Thermodynam., 100, 165, 2016
  43. Aftabuzzaman M, Islam MM, Nasiruddin, Rima FR, Islam MN, Ali MA, J. Chem. Thermodynam., http://dx.doi.org/10.1016/j.jct.2015.12.030.
  44. Alonso I, Mozo I, de la Fuente I, Gonzalez JA, Cobos JC, J. Chem. Eng. Data, 55(12), 5400, 2010
  45. Kumar S, Jeevanandham P, J. Mol. Liq., 174, 34, 2012
  46. Pandiyan V, Oswal SL, Vasantharani, Thermochim. Acta, 518, 36, 2011
  47. Sharma VK, Solanki S, Bhagour S, Sharma D, J. Mol. Liq., 188, 258, 2013
  48. Vasundhara P, Rao CN, Venkatramana L, Sivakumar K, Venkateswarlu P, Gardas RL, J. Mol. Liq., 202, 158, 2015