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Enthalpies of combustion, vapour pressures, and enthalpies of sublimation of the 1,5- and 1,8-diaminonaphthalenes

2009; Elsevier BV; Volume: 42; Issue: 3 Linguagem: Inglês

10.1016/j.jct.2009.09.009

1096-3626

Manuel A.V. Ribeiro da Silva, Ana I.M.C. Lobo Ferreira, Ana Filipa L.O.M. Santos, Cristiana M.A. Ferreira, D. Barros, Joana Reis, José C. S. Costa, Maria Miguel G. Calvinho, Sónia Rocha, Sónia P. Pinto, Sonia Freire, Suzete Almeida, Vanessa Guimarães, Vasco N.M. Almeida,

Phase Equilibria and Thermodynamics

Abstract The standard (p∘ = 0.1 MPa) molar enthalpies of formation, in the crystalline state, of 1,5-diaminonaphthalene and 1,8-diaminonaphthalene were derived from the standard molar energies of combustion, in oxygen, at T = 298.15 K, measured by static-bomb combustion calorimetry. The Knudsen mass-loss effusion technique was used to measure the dependence of the vapour pressure of the solid isomers of diaminonaphthalene with the temperature, from which the standard molar enthalpies of sublimation were derived using the Clausius–Clapeyron equation. - Δ c U m ∘ ( cr ) / ( kJ · mol - 1 ) Δ f H m ∘ ( cr ) / ( kJ · mol - 1 ) Δ cr g H m ∘ / ( kJ · mol - 1 ) 1,5-Diaminonaphthalene 5402.7 ± 2.2 42.1 ± 2.6 122.5 ± 0.9 1,8-Diaminonaphthalene 5425.9 ± 2.3 65.4 ± 2.6 99.0 ± 0.7 Combining these two experimental values, the gas-phase standard molar enthalpies of formation, at T = 298.15 K, were derived and compared with those estimated using two different empirical methods of Δ f H m ∘ ( g ) estimation: the Cox scheme and the Benson’s Group Method. Moreover, the standard (p∘ = 0.1 MPa) molar entropies and Gibbs energies of sublimation, at T = 298.15 K, were derived for the two diaminonaphthalene isomers.