Synthesis of diketopiperazine: A kinetic study by means of thermoanalytical

ILEANA DANIELA LICK; MARÍA LUISA VILLALBA; LUCIANA GAVERNET

THERMOCHIMICA ACTA

ELSEVIER SCIENCE BV

Año: 2011 vol. 527 p. 143 - 147

0040-6031

The enalapril maleate (EM) decomposition to diketopiperazine was monitored in helium flow by thermogravimetry at different heating rates between 0.2 and 5 ◦C min−1. The activation energy value was obtained (198 kJ mol−1) from the Kissinger–Akahira–Sunose isoconversional method. Isothermal experiments were simulated (125, 130, 135 and 155 ◦C) using the model-free method, employing only the activation energy value. The reaction model of the process was studied by means of the master-plot method. The reaction mechanism depends on the temperature; for experiments below 235 ◦C, the probable mechanism is nucleation. Instead, when the temperature overcomes the EM melting point, the reaction occurs in liquid state and its kinetics is better described by first order reaction. To avoid the complexity of model changes, experimental results are fitted using the model-free method.◦C min−1. The activation energy value was obtained (198 kJ mol−1) from the Kissinger–Akahira–Sunose isoconversional method. Isothermal experiments were simulated (125, 130, 135 and 155 ◦C) using the model-free method, employing only the activation energy value. The reaction model of the process was studied by means of the master-plot method. The reaction mechanism depends on the temperature; for experiments below 235 ◦C, the probable mechanism is nucleation. Instead, when the temperature overcomes the EM melting point, the reaction occurs in liquid state and its kinetics is better described by first order reaction. To avoid the complexity of model changes, experimental results are fitted using the model-free method.−1) from the Kissinger–Akahira–Sunose isoconversional method. Isothermal experiments were simulated (125, 130, 135 and 155 ◦C) using the model-free method, employing only the activation energy value. The reaction model of the process was studied by means of the master-plot method. The reaction mechanism depends on the temperature; for experiments below 235 ◦C, the probable mechanism is nucleation. Instead, when the temperature overcomes the EM melting point, the reaction occurs in liquid state and its kinetics is better described by first order reaction. To avoid the complexity of model changes, experimental results are fitted using the model-free method.◦C) using the model-free method, employing only the activation energy value. The reaction model of the process was studied by means of the master-plot method. The reaction mechanism depends on the temperature; for experiments below 235 ◦C, the probable mechanism is nucleation. Instead, when the temperature overcomes the EM melting point, the reaction occurs in liquid state and its kinetics is better described by first order reaction. To avoid the complexity of model changes, experimental results are fitted using the model-free method.◦C, the probable mechanism is nucleation. Instead, when the temperature overcomes the EM melting point, the reaction occurs in liquid state and its kinetics is better described by first order reaction. To avoid the complexity of model changes, experimental results are fitted using the model-free method.