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Low-Temperature Heat Capacities and Thermodynamic Properties of 2-Aminopyridine
Corresponding Author(s) : Chun-Sheng Zhou
Asian Journal of Chemistry,
Vol. 28 No. 3 (2016): Vol 28 Issue 3
Abstract
Low-temperature heat capacities of 2-aminopyridine have been measured by a precision automatic adiabatic calorimeter over the temperature range from 78 to 370 K. A solid-liquid phase transition was observed from 315 to 335 K. The peak temperature, molar enthalpy and entropy of the solid-liquid phase transition were determined to be: (330.09 ± 0.01) K, (18.33 ± 0.05) kJ mol-1 and (55.53 ± 0.14) J K-1 mol-1, respectively. In addition, the mole fraction purity, the melting temperature of the given sample and that of pure sample were calculated to be (99.54 ± 0.06) %, (330.20 ± 0.01) K and (330.43 ± 0.01) K by means of fractional melting method. The results showed that the melting temperature of the sample from adiabatic calorimetry agreed basically with that from theoretical analysis of the purity.
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- J. Chen, R.J. Qu and Y.Z. Niu, J. Ludong Univ. (Nat. Sci. Ed.), 22, 333 (2006).
- J. Bickerton, G. Pilcher and G. Al-Takhin, J. Chem. Thermodyn., 16, 373 (1984); doi:10.1016/0021-9614(84)90175-7.
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- D. Wei and L. Chen, J. Chem. Eng. Data, 54, 1129 (2009); doi:10.1021/je800841v.
- D. Wei and L. Chen, J. Chem. Eng. Data, 54, 1098 (2009); doi:10.1021/je800768x.
- J. Buckingham and S.M. Donaghy, Dictionary of Organic Compounds, Published by Chapman & Hall: New York, edn 5, Vol. 1, p. 796 (1982).
- Z.C. Tan, G.Y. Sun, Y. Sun, A. Yin, W. Wang, J. Ye and L. Zhou, J. Therm. Anal. Calorim., 45, 59 (1995); doi:10.1007/BF02548664.
- Z.C. Tan, B.P. Liu, J.B. Yan and L.X. Sun, J. Comput. Appl. Chem., 20, 264 (2003).
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- J.H. Badley, J. Phys. Chem., 63, 1991 (1959); doi:10.1021/j150582a002.
- S.V.R. Mastrangelo and R.W. Dornte, J. Am. Chem. Soc., 77, 6200 (1955); doi:10.1021/ja01628a037.
References
J. Chen, R.J. Qu and Y.Z. Niu, J. Ludong Univ. (Nat. Sci. Ed.), 22, 333 (2006).
J. Bickerton, G. Pilcher and G. Al-Takhin, J. Chem. Thermodyn., 16, 373 (1984); doi:10.1016/0021-9614(84)90175-7.
W. Brostow, J.C. Iniguez, M.A. Shmorhun and J.A. Valdez, Mater. Chem. Phys., 12, 557 (1985); doi:10.1016/0254-0584(85)90042-2.
C.W.N. Cumper, R.F.A. Ginman, D.G. Redford and A.I. Vogel, J. Chem. Soc., 1731 (1963); doi:10.1039/jr9630001731.
D. Wei and L. Chen, J. Chem. Eng. Data, 54, 1129 (2009); doi:10.1021/je800841v.
D. Wei and L. Chen, J. Chem. Eng. Data, 54, 1098 (2009); doi:10.1021/je800768x.
J. Buckingham and S.M. Donaghy, Dictionary of Organic Compounds, Published by Chapman & Hall: New York, edn 5, Vol. 1, p. 796 (1982).
Z.C. Tan, G.Y. Sun, Y. Sun, A. Yin, W. Wang, J. Ye and L. Zhou, J. Therm. Anal. Calorim., 45, 59 (1995); doi:10.1007/BF02548664.
Z.C. Tan, B.P. Liu, J.B. Yan and L.X. Sun, J. Comput. Appl. Chem., 20, 264 (2003).
Z.C. Tan, Q. Shi, B.P. Liu and H.T. Zhang, J. Therm. Anal. Calorim., 92, 367 (2008); doi:10.1007/s10973-007-8954-2.
D.A. Ditmars, S. Ishihara, S.S. Chang, G. Bernstein and E.D. West, J. Res. Natl. Bur. Stand., 87, 159 (1982); doi:10.6028/jres.087.012.
Y.Y. Di, Z.C. Tan, X.M. Wu, S.H. Meng and S.S. Qu, Thermochim. Acta, 356, 143 (2000); doi:10.1016/S0040-6031(00)00479-2.
J.H. Badley, J. Phys. Chem., 63, 1991 (1959); doi:10.1021/j150582a002.
S.V.R. Mastrangelo and R.W. Dornte, J. Am. Chem. Soc., 77, 6200 (1955); doi:10.1021/ja01628a037.