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Acoustical studies of binary liquid mixtures of p-chlorotoluene in benzene at different temperatures

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Ultrasonic velocities (U), densities (ρ), and coefficient of viscosities (η) are measured for binary mixtures containing (i) p-chlorotoluene and (ii) benzene at 303.15 K, 308.15 K, 313.15 K and 318.15 K to understand the molecular interaction. Various acoustical parameters such as adiabatic compressibility (βad), free length (Lf), acoustic impedance (Z), free volume (Vf), molar volume (Vm), Rao’s constant (R), Wada’s constant (W) and internal pressure (πi), are calculated from the measured values of U, ρ, and η. The trend in acoustical parameters also substantiates to asses strong molecular interactions.
Rocznik
Tom
Strony
25--37
Opis fizyczny
Bibliogr. 23 poz., rys., tab.
Twórcy
autor
  • Ultrasonic Laboratory, Department of Physics, Andhra University, Visakhapatnam - 530003, India
autor
  • Ultrasonic Laboratory, Department of Physics, Andhra University, Visakhapatnam - 530003, India
autor
  • Ultrasonic Laboratory, Department of Physics, Andhra University, Visakhapatnam - 530003, India
autor
  • Physics Department, St. Theresa College, Eluru, Andhra Pradesh, India
Bibliografia
  • [1] D. Vengatesulu, D. K. Prabhakara Rao, J. Acous. Soc. Ind. 1(4) (1999) 320.
  • [2] S. J. Askar Ali, K. Rajathi, A. Rajendran, J. Chem. Pharm. Res. 3(5) (2011) 348-358.37
  • [3] V. D. Bhandarkkar, O. P. Chimankar, N. R. Pawar, J. Chem. Pharm. Res. 2(4) (2010) 873-877.
  • [4] D. Bala Karuna Kumar, K. Rayapa Reddy, G. Srinivasa Rao, G. V. Rama Rao, C. Rambabu, J. Chem. Pharm. Res. 3(5) (2011) 274-280.
  • [5] G. V. Ramarao, A. V. Sarma, C. Rambabu, Ind. J. Pure Appl. Phys. 42 (2004) 820-826.
  • [6] G. V. Ramarao, A. V. Sarma, D. Ramachandran, C. Rambabu, Ind. J. Pure Appl. Phys. 43 (2005) 602-608.
  • [7] G. V. Ramarao, A. V. Sarma, P. B. Sandhyasri, C. Rambabu, Ind. J. Pure Appl. Phys. 45 (2007) 135-142.
  • [8] K. Sreekanth, D. S. Kumar, M. Kondaiah, D. Krishnarao, J. Chem. Pharm. Res. 3(4) (2011) 29-41.
  • [9] R. Venis, R. Rajkumar, J. Chem. Pharm. Res. 3(2) (2011) 878-885.
  • [10] Shilpa Mirikar, P. Pravina Pawar, K. Govind Bichile, J. Chem. Pharm. Res. 3(5) (2011) 306-310.
  • [11] A. K. Nain, J. Chem. Thermodynamics 59 (2013) 49-64.
  • [12] M. Aravinthraj, S. Venkatesan, D. Meera, J. Chem. Pharm. Res. 3(2) (2011) 623.
  • [13] P. S. Agrawal, M. S. Wagh, L. J. Paliwal, Archives of Applied Science Research 3(2) (2011) 29.
  • [14] R. J. Forte, W. R. Moore, Trans. Faraday Soc. 61 (1965) 2102.
  • [15] P. B. Agrawal, Mohd Indrees Mohd Siddique, M. L. Narwade, Ind. J. Chem. 42A(5) (2003) 1050.
  • [16] S. J. Askar Ali, J. Chem. Pharm. Res. 4(1) (2012) 617-632.
  • [17] N. Santhi, P. Sabarathinam, G. Alamelumangai, J. Madhumitha, M. Emayavaramban, International Letters of Chemistry, Physics and Astronomy 5 (2012) 1-7.
  • [18] N. Santhi, P. L. Sabarathinam, G. Alamelumangai, J. Madhumitha, M. Emayavaramban, International Letters of Chemistry, Physics and Astronomy 5 (2012) 59-71.
  • [19] N. Santhi, P. L. Sabarathinam, J. Madhumitha, G. Alamelumangai, M. Emayavaramban, International Letters of Chemistry, Physics and Astronomy 2 (2013) 18-35.
  • [20] M. Durga Bhavani, A. Ratnakar, Ch. Kavith, International Letters of Chemistry, Physics and Astronomy 5 (2013) 1-6.
  • [21] S. S. J. Srinivas, B. Tulasi Koteswari Bai, K. Babu Rao, K. Narendra, M. Sarath Babu, International Letters of Chemistry, Physics and Astronomy 10(2) (2013) 151-158.
  • [22] C. H. Srinivasu, K. Anil Kumar, S. K. Fakruddin, K. Narendra, T. Anjaneyulu, International Letters of Chemistry, Physics and Astronomy 13 (2013) 1-7.
  • [23] G. Alamelumangai, N. Santhi, International Letters of Chemistry, Physics and Astronomy 5 (2014) 124-133.
Uwagi
Autor Jyosthna A. N nie ma przydzielonej afiliacji
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-f8cdb876-ec68-4841-bc5e-d1cf037d86d5
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