2015
DOI: 10.1007/s10973-015-5036-8
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Energies of combustion and enthalpies of formation of 5-methyl-5-phenylhydantoin and 5,5-diphenylhydantoin

Abstract: The standard molar energies of combustion D c U°(cr, 298.15 K) of 5-methyl-5-phenylhydantoin and 5,5-diphenylhydantoin were obtained by static-bomb combustion calorimetry. The calorimeter was re-calibrated in order to determine the energy equivalent, and the valued obtained was e (calor) = (10,150.8 ± 1.2) J K -1 . The heat capacities and purities of the compounds studied in present work were determined using a differential scanning calorimeter. The molar combustion energies obtained for 5-methyl-5-phenylhydan… Show more

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Cited by 7 publications
(1 citation statement)
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“…For example, El-Sayed [16] reported the enthalpies of combustion and formation of hydantoin; Silva et al [17] described a comprehensive computational and experimental energy study on hydantoin and 2-thiohydantoin. Recently, our research group has carried out thermochemical studies on the enthalpies of sublimation and enthalpies of formation in the condensed and gas phase of 5-methylhydantoin, 5-methyl-5-phenylhydantoin, and 5,5-diphenylhydantoin [18,19]. Nogueira et al [20] conducted a study on the spectroscopic characterization and thermal behavior of 1-methylhydantoin.…”
Section: Introductionmentioning
confidence: 99%
“…For example, El-Sayed [16] reported the enthalpies of combustion and formation of hydantoin; Silva et al [17] described a comprehensive computational and experimental energy study on hydantoin and 2-thiohydantoin. Recently, our research group has carried out thermochemical studies on the enthalpies of sublimation and enthalpies of formation in the condensed and gas phase of 5-methylhydantoin, 5-methyl-5-phenylhydantoin, and 5,5-diphenylhydantoin [18,19]. Nogueira et al [20] conducted a study on the spectroscopic characterization and thermal behavior of 1-methylhydantoin.…”
Section: Introductionmentioning
confidence: 99%