RT info:eu-repo/semantics/article
T1 Thermodynamics of mixtures containing amines. XVII. HmE and VmE measurements for benzylamine + heptane or + 1-alkanol mixtures at 298.15 K. Application of the DISQUAC and ERAS models
A1 Sanz del Soto, Luis Felipe
A1 González López, Juan Antonio Mariano
A1 Hevia de los Mozos, Luis Fernando
A1 García de la Fuente, Isaías Laudelino
A1 Cobos Hernández, José Carlos
K1 Termodinámica
K1 2213 Termodinámica
AB Excess molar enthalpies, HmE , at 298.15 K and 0.1 MPa have been measured by means of a Tian-Calvet microcalorimeter for the systems benzylamine (phenylmethanamine) + heptane, or + methanol, or + 1-propanol, or + 1-pentanol, or + 1-heptanol, or + 1-decanol. In addition, excess molar volumes, VmE, at the same conditions have been also determined using a densimeter Anton Paar model DSA 5000 for the benzylamine + heptane mixture. The HmE of this solution is large and positive since at 298.15 K the system temperature is close to its upper critical solution temperature. Thus, systems with n-alkanes show positive deviations from the Raoult’s law. The measured |VmE| values are low, indicating the existence of large structural effects. HmE values of mixtures involving 1-alkanols are large and negative. That is, interactions between unlike molecules are dominant and the systems are characterized by negative deviations from Raoult’s law. It is shown that the enthalpy of the hydrogen bonding between molecules of 1-alkanol and benzyalmine are more negative than those between 1-alkanol molecules. The VmE values of the systems with 1-alkanols are also large and negative, and are determined mainly by interactional effects since they increase in line with HmE and with the alcohol size. The different contributions to HmE have been evaluated. The systems have been studied using the DISQUAC and ERAS models. ERAS describes correctly the VmE function. DISQUAC largely improves ERAS results on HmE or on excess molar heat capacities at constant pressure for the mixtures with 1-alkanols, which underlines that physical interactions are very relevant in such solutions.
PB Elsevier
SN 0378-3812
YR 2022
FD 2022
LK https://uvadoc.uva.es/handle/10324/69164
UL https://uvadoc.uva.es/handle/10324/69164
LA spa
NO Fluid Phase Equilibria, 2022, 558, 113460
DS UVaDOC
RD 22-nov-2024