Density and surface tension of binary mixtures of acetonitrile + 1-alkanol at 293.15 K

Journal of Chemical and Engineering Data

Volumn 51, Issue 3, 2006, Pages 1039-1042

  Tahery, Reza ^a   Modarress, Hamid ^a   Satherley, John ^b  

^a AMIRKABIR UNIVERSITY OF TECHNOLOGY   (Iran)

^b UNIVERSITY OF LIVERPOOL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ACETONITRILE; ATMOSPHERIC PRESSURE; DENSITY (SPECIFIC GRAVITY); ETHANOL; MOLECULAR DYNAMICS; SURFACE TENSION;

INTERMOLECULAR INTERACTION; MOLAR VOLUME; POLYNOMIAL EQUATIONS; REDLICH-KISTER POLYNOMIAL EQUATION;

BINARY MIXTURES;

EID: 33744480318     PISSN: 00219568     EISSN: None     Source Type: Journal    
DOI: 10.1021/je050519g     Document Type: Article

References (42)

1. Kim, E. S.; Marsh, K. N. Excess volumes for 2-methly-2-propanol + water at 5 K intervals from 303.15 to 323.15 K. J. Chem. Eng. Data 1988, 33, 288-292.
2. Barthel, J.; Gores, H. J.; Schmeer, G.; Wachter, R. Topics in Current Chemistry; Springer: New York, 1983; Vol. III, p 33.
3. Fernández-Piérola, I.; Horta, A. Cosolvents of PMMA. Makromol. Chem. 1981, 182, 1705-1714.
4. Torres, R. B.; Francesconi, A. Z.; Volpe, P. L. O. Thermodynamics of binary liquid mixtures: application of the Prigogine-Flory-Patterson theory to excess molar volumes of acetonitrile + 1-alkanol systems. J. Mol. Liq. 2004, 110, 81-85.
5. Grguric, I. R.; Tasic, A. Z.; Djordjevic, B. D.; Kijevcanin, M. L.; Serbanovic, S. P. Excess molar volume of the acetonitrile plus alcohol systems at 298.15 K. Part I: Density measurements for acetonitrile plus methanol, plus ethanol systems. J. Serb. Chem. Soc. 2002, 67, 581-586.
6. Grguric, I. R.; Kijevcanin, M. L.; Djordjevic, B. D.; Tasic, A. Z.; Serbanovic, S. P. Excess molar volume of acetonitrile plus alcohol systems at 298.15 K. Part II: Correlation by cubic equation of state. J. Serb. Chem. Soc. 2003, 68, 47-56.
7. Torres, R. B.; Francesconi, A. Z.; Volpe, P. L. O. Experimental study and modeling using the ERAS-model of the excess molar volume of acetonitrile - alkanol mixtures at different temperatures and atmospheric pressure. Fluid Phase Equilib. 2003, 210, 287-306.
8. Martins, A.; Laurent, R.; Aznarez, S. B. Interactional parameters fitting in thermodynamics models. Ecletica Quim. 2000, 25, 41-50.
9. Saha, N.; Das, B.; Hazra, D. K. Viscosities and excess molar volumes for acetonitrile + methanol at 298.15, 308.15, and 318.15 K. J. Chem. Eng. Data 1995, 40, 1264-1266.
10. 5) binary mixtures with acetonitrile. J. Chem. Eng. Data 1986, 31, 152-154.
11. Pina, C. G.; Francesconi, A. Z. New applications of the ERAS model: excess volumes of binary liquid mixtures of 1-alkanols with acetonitrile. Fluid Phase Equilib. 1998,143, 143-152.
12. Cibulka, I.; Nguyen, D.; Holub, R. Excess molar volumes of (an alkanol + acetonitrile) at 298.15 and 308.15 K. J. Chem. Thermodyn. 1984, 16, 159-164.
13. Nikam, P. S.; Shirsat, L. N.; Hasan, M. M. Density and viscosity studies of binary mixtures of acetonitrile with methanol, ethanol, propan-1-ol, propan-2-ol, butan-1-ol, 2-methylpropan-1-ol, and 2-methylpropan-2-ol at (298.15, 303.15, 308.15, and 313.15) K. J. Chem. Eng. Data 1998, 43, 732-737.
14. Nagata, I.; Tamura, K. Thermodynamics of solutions containing acetonitrile and 1-butanol. Thermochem. Acta 1988, 124, 53-64.
15. Nagata, I.; Tamura, K. Excess molar enthalpies of (propan-1-ol or propan-2-ol + acetonitrile), (propan-1-ol or propan-2-ol + chlorobenzene), and (propan-1-ol or propan-2-ol + acetonitrile + chlorobenzene) at 298.15 K. J. Chem. Thermodyn. 1988, 20, 87-93.
16. Garriga, R.; Putze, I.; Perez, P.; Gracia, M. Vapour pressures at several temperatures fand excess functions at T = 298.15 K of (butanenitrile + ethanol or butan-1-ol). J. Chem. Thermodyn. 1995, 27, 481-491.
17. Garriga, R.; Sanchez, F.; Perez, P.; Gracia, M. Vapour pressures at several temperatures T and excess functions at T = 298.15 K of (butanenitrile + propan-1-ol or propan-2-ol). J. Chem. Thermodyn. 1995, 27, 887-895.
18. Garriga, R.; Perez, P.; Gracia, M. Vapour pressures at several temperatures T and excess functions at T= 298.15 K of (butanenitrile + hexan-1-ol or octan-1-ol). J. Chem. Thermodyn. 1995, 27, 1057-1066.
19. Doman'ska, U.; Marciniak, M. Experimental (solid + liquid) and (liquid + liquid) equilibria and excess molar volume of alkanol + acetonitrile, propanenitrile, and butanenitrile mixtures. J. Chem. Eng. Data 2005, 50, 2035-2044.
20. Cunningham G. P., Vidulich G. A., Robert L. K.; Several properties of acetonitrile-water, acetonitrile-methanol, and ethylene carbonate-water systems. J. Chem. Eng. Data 1967, 12 (3), 336-337.
21. Martinez, S.; Garriga, R.; Perez, P.; Gracia, M. Densities and viscosities of binary mixtures of butanenitrile with butanol isomers at several temperatures. J. Chem. Eng. Data 2000, 45, 1182-1188.
22. Garriga, R.; Sanchez, F.; Perez, P.; Gracia, M. Excess Gibbs free energies at eight temperatures and excess enthalpies and volumes at T = 298.15 K for butanenitrile + 2-butanol. J. Chem. Eng. Data 1997, 42, 78-83.
23. Garriga, R.; Sanchez, F.; Perez, P.; Gracia, M. Excess Gibbs free energies at several temperatures and excess enthalpies and volumes at 298.15 K of butanenitrile with 2-methyl-1-propanol or 2-methyl-2-propanol. Fluid Phase Equilib. 1997, 130, 195-206.
24. Garriga, R.; Ilarraza, J.; Perez, P.; Gracia, M. Excess functions at T = 298.15 K of (butanenitrile + methanol, + pentan-1-ol, + heptan-l-ol, + nonan-1-ol, or + decan-1-ol). J. Chem. Thermodyn. 1996, 28, 233-243.
25. Letcher, T. M.; Naicker, P. K. Excess molar enthalpies and excess molar volumes of (an alkanol + nitrile compound) at T = 298.15 K and p = 0.1 MPa. J. Chem. Thermodyn. 2001, 33, 1035-1047.
26. Paez, S.; Contreras, M. Densities and viscosities of binary mixtures of 1-propanol and 2-propanol with acetonitrile. J. Chem. Eng. Data 1989, 34, 455-459.
27. Ku, H. C.; Tu, C. H. Density and viscosity of binary mixtures of propan-2-ol, 1-chlorobutane, and acetonitrile. J. Chem. Eng. Data 1998, 43, 465-468.
28. Beaton, C. F.; Hewitt, G. F. Physical Property Data for the Design Engineer, Hemisphere Publishing Corp.: New York, 1989.
29. CRC Handbook of Chemistry and Physics, 74th ed.; Lide, D. R., Ed.; CRC Press: Boca Raton, FL, 1993-1994.
30. Djojoputro, H.; Ismadji, S. Density and viscosity of binary mixtures of ethyl-2-methylbutyrate and ethyl hexanoate with methanol, ethanol, and 1-propanol at (293.15, 303.15, and 313.15) K. J. Chem. Eng. Data 2005, 50, 1343-1347.
31. Azizian, S.; Bashavard, N. Surface tension of dilute solutions of linear alcohols in benzyl alcohol. J. Chem. Eng. Data 2005, 50, 1303-1307.
32. Indraswati, N.; Filicia Wicaksana, M.; Hindarso, H. Density and viscosity for a binary mixture of ethyl valerate and hexyl acetate with 1-pentanol and 1-hexanol at 293.15 K. 303.15 K. and 313.15 K. J. Chem. Eng. Data 2001, 46, 134-137.
33. Pai, Y. H.; Chen, L. J. Viscosity and density of dilute aqueous solutions of 1-pentanol and 2-methyl-2-butanol. J. Chem. Eng. Data 1998, 43, 665-667.
34. Riddick, J. A.; Bunger, W. B.; Sakano, T. K. Organic Solvents, Physical Properties and Methods of Purification, 4th ed.; John Wiley & Sons: New York, 1986.
35. TRC Thermodynamic Tables, Non-Hydrocarbons; Thermodynamic Research Center, Texas A&M University: College Station, TX, 1993.
36. Jasper, J. J. The surface tension of pure liquid compounds. J. Phys. Chem. Ref. Data 1972, 841-984.
37. Vazquez, G.; Alvarez, E.; Navaza, J. M. Surface tension of alcohol + water from 20 to 50 °C. J. Chem. Eng. Data 1995, 40, 611-614.
38. Azizian, S.; Hemmati, M. Surface tension of binary mixtures of ethanol + ethylene glycol from 20 to 50 °C. J. Chem. Eng. Data 2003, 48, 662-663.
39. Lange's Handbook of Chemistry, 13th ed.; Dean, J. A., Lange, N. A., Eds.; McGraw-Hill Inc.: New York, 1985.
40. Girault, H. H. J., Schiffrin, D. J., Smith, B. D. V. The measurement of interfacial tension of pendant drops using a video image profile digitizer. J. Colloid Interface Sci. 1984, 101, 257-266.
41. Walas, S. M.; Phase Equilibria In Chemical Engineering; Buttersworth: New York, 1985; p 184.
42. Mecke, R. Infrared spectra of hydroxylic compounds. Discuss. Faraday Soc. 1950, 9, 161-177.