Abstract
By high precision dynamic calorimetry the temperature dependences of heat capacity C p 0 = f ( T ) for dimer of C 60 , orthorhombic and rhombohedral polymerized phases of fullerene C 60 were determined in the temperature range 300–650 K. Besides, endothermic transformations caused by the depolymerization of the polymerized (dimeric) phases of C 60 were studied and their standard thermodynamic characteristics a temperature interval, enthalpy, entropy and Gibbs function were analyzed. Based on the thermodynamic and oscillation spectroscopy data, it was established that the depolymerization proceeds completely and the products formed are a monomer fcc phase of C 60 . From the data of the present work and the heat capacity values measured by us earlier in a low-temperature interval, the thermodynamic functions of the substances, viz. the heat capacity C p 0 ( T ), enthalpy H 0 ( T )− H 0 (0), entropy S 0 ( T )− S 0 (0) and Gibbs function G 0 ( T )− H 0 (0), were calculated over the range from T →0 to (380–490) K at standard pressure. The results were discussed taking into account literature data. A sequence of a relative thermodynamic stability at 298.15 K and atmosphere pressure of the crystalline polymerized C 60 phases was arranged.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
