Calorimetric determination of enthalpies for the proton ionization of N,N-bis[2-hydroxyethyl]-2-aminoethanesulfonic acid (BES) and N-tris[hydroxymethyl]methyl-2-aminoethanesulfonic acid (TES) in water-methanol mixtures

Thermochimica Acta

Volumn 411, Issue 1, 2004, Pages 91-94

  Bulos, B N ^a   Jumean, F H ^a  

^a AMERICAN UNIVERSITY OF SHARJAH   (United Arab Emirates)

Author keywords

BES; Calorimetry; Proton ionization; TES

Indexed keywords

2 [BIS(2 HYDROXYETHYL)AMINO]ETHANESULFONIC ACID; 2 [TRIS(HYDROXYMETHYL)METHYLAMINO]ETHANESULFONIC ACID; AMINO ACID DERIVATIVE; BUFFER; HYDROXYL GROUP; METHANOL; METHYL GROUP; SOLVENT; SULFONIC ACID DERIVATIVE; UNCLASSIFIED DRUG; WATER;

ADDITION REACTION; ARTICLE; BIOCHEMISTRY; CONCENTRATION RESPONSE; DIFFERENTIAL SCANNING CALORIMETRY; ENTHALPY; FRACTIONATION; IONIZATION; MOLECULAR INTERACTION; PROTON TRANSPORT; REACTION ANALYSIS; STEADY STATE; STRUCTURE ANALYSIS; TEMPERATURE DEPENDENCE; THERMAL ANALYSIS; THERMODYNAMICS;

EID: 0742324384     PISSN: 00406031     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tca.2003.08.003     Document Type: Article

References (29)

1. R.G. Bates, Determination of pH, second ed., Wiley, New York, 1973 (Chapter 7).
2. Bates R.G., Roy R.N., Robinson R.A. J. Solut. Chem. 3:1974;905.
3. Roy R.N., Gibbons J.J., Snelling R. J. Solut. Chem. 6:1977;475.
4. Das R.C., Dash U.N., Panda K.N. J. Chem. Soc., Faraday I. 76:1980;2152.
5. Jumean F.H., Abdelrahim Z. Ann. Chim. (Rome). 82:1992;49.
6. Jumean F.H., Abdelrahim Z. Arab. J. Sci. Eng. 19:1994;77.
7. Ramette R.W. J. Chem. Ed. 61:1984;76.
8. Harned H.S., Hamer W.J. J. Am. Chem. Soc. 55:1933;2194.
9. Bertrand G.L., Millero F.J., Wu C.H., Hepler L.G. J. Phys. Chem. 70:1966;699.
10. Kido H., Fernelius W.C. J. Phys. Chem. 65:1961;574.
11. J.J. Christensen, R.M. Izatt, L.D. Hansen, in: G.D. Fasman (Ed.), Handbook of Biochemistry and Molecular Biology, third ed., vol. I, CRC Press, Boca Raton, FL, 1976, pp. 260-261.
12. V.B. Parker, in: Thermal Properties of Aqueous Uni-Univalent Electrolytes, Natl. Stand. Ref. Data Ser. -Natl. Bur. Stand. (US) 2, US Government Printing Office, Washington, DC, 1965.
13. F. Franks, in: F. Franks (Ed.), Physiochemical Processes in Mixed Aqueous Solvents, Elsevier, New York, 1967, pp. 50-79.
14. Hales J.D., Izatt R.M., Christensen J.J. J. Phys. Chem. 67:1963;2605.
15. Vanderzee C.E., Swanson J.A. J. Phys. Chem. 67:1963;2608.
16. Antikainen P.J. Suomen Kemistilehti. B29:1956;14.
17. Olofsson G., Hepler L. J. Solut. Chem. 4:1975;127.
18. Arnek R., Patel C.C. Acta Chem. Scand. 22:1968;1097.
19. Handbook of Chemistry and Physics, 83rd ed. CRC Press, Boca Raton, FL, pp. 2002-2003 (Section 8).
20. Lumme P., Lahermo P., Tummavuori T. Acta Chem. Scand. 19:1965;2175.
21. Goldberg R.N., Kishore N., Lennen R.M. J. Phys. Chem. Ref. Data. 31:2002;231.
22. Fukada H., Takahashi K. Proteins: Struct. Funct. Genet. 33:1998;159.
23. McGlothlin C.D., Jordan J. J. Anal. Lett. 9:1976;245.
24. Roig T., Backman P., Olofsson G. Acta Chem. Scand. 47:1993;899.
25. Vega C.A., Bates R.G. Anal. Chem. 48:1976;1293.
26. Roy R.N., Moore C.P., Lord P., Murad D., Roy L.N., Good W.S., Niederschmidt J., Kuhler K.M. J. Chem. Thermodyn. 29:1997;1323.
27. D. Feakins, pp. 71-90 (in ref. 3).
28. R.G. Bates, R.A. Robinson, in: B.E. Conway, R.G. Barradas (Eds.), Chemical Physics of Ionic Solutions, Wiley, New York, 1966, pp. 211-235.
29. Hansen L.D., Hepler L.G. Can. J. Chem. 50:1972;1030.