dc.contributorUniversidade Estadual Paulista (Unesp)
dc.contributorUniversity of Huddersfield
dc.date.accessioned2019-10-06T17:18:25Z
dc.date.accessioned2022-12-19T19:08:40Z
dc.date.available2019-10-06T17:18:25Z
dc.date.available2022-12-19T19:08:40Z
dc.date.created2019-10-06T17:18:25Z
dc.date.issued2019-10-01
dc.identifierThermochimica Acta, v. 680.
dc.identifier0040-6031
dc.identifierhttp://hdl.handle.net/11449/190593
dc.identifier10.1016/j.tca.2019.178353
dc.identifier2-s2.0-85071019311
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/5371631
dc.description.abstractIn the present work, the thermal behavior of Lornoxicam drug was studied under oxidizing (air) and pyrolysis (N2) atmospheres using simultaneous thermogravimetry and differential scanning calorimetry (TG-DSC), differential scanning calorimetry (DSC), Hot Stage Microscopy (HSM) and Evolved Gas Analysis (EGA) in the form of thermogravimetry coupled to infrared spectroscopy (TG-FTIR) and mass spectrometry (TG-MS). The thermal degradation product formed at different temperatures were examined using liquid chromatography coupled to mass spectrometry (LC–MS) and Powder X-Ray Diffraction (PXRD). The thermal study showed that the drug does not melt, partially amorphized on heating, it is thermally stable to 205 °C and undergoes thermal decomposition in two overlapping mass loss steps. Furthermore, the DSC and MS techniques suggest that thermal degradation processes are very complex, which occur with the release of gaseous products HCN, SO2, COS, CO2, N2O and CO and formation of three intermediate in the thermal residue.
dc.languageeng
dc.relationThermochimica Acta
dc.rightsAcesso aberto
dc.sourceScopus
dc.subjectEGA
dc.subjectHSM
dc.subjectLC–MS/MS
dc.subjectLornoxicam
dc.subjectThermal degradation
dc.titleLornoxicam drug—A new study of thermal degradation under oxidative and pyrolysis conditions using the thermoanalytical techniques, DRX and LC-MS/MS
dc.typeArtículos de revistas


Este ítem pertenece a la siguiente institución