Thermal analysis of paraffins by calorimetry

Citation
J. Pak et al., Thermal analysis of paraffins by calorimetry, THERMOC ACT, 357, 2000, pp. 259-266
Citations number
22
Categorie Soggetti
Spectroscopy /Instrumentation/Analytical Sciences
Journal title
THERMOCHIMICA ACTA
ISSN journal
00406031 → ACNP
Volume
357
Year of publication
2000
Pages
259 - 266
Database
ISI
SICI code
0040-6031(20000814)357:<259:TAOPBC>2.0.ZU;2-M
Abstract
Paraffins of sufficient chain length can serve as model compounds for flexi ble macromolecules. They crystallize almost completely and do not suffer fr om chain folding as long as their chain length is less than about 10 nm. Th e melting and crystallization of a paraffin, C50H102 (n-pentacontane), was analyzed as such a model compound with both, standard differential scanning calorimetry (DSC) and temperature-modulated DSC (TMDSC) using saw-tooth mo dulation and quasi-isothermal modulation with very small amplitude (0.05 K) . The supercooling due to nucleation was shown to be strongly cooling-rate dependent. There was practically no supercooling needed for crystallization from the melt with cooling rates up to 10 K/min, and values of up to 10 K were found for cooling rates of 30 K/min. Melting was completed within 1 K with quasi-isothermal modulation, but 66% of total melting occurred over a much narrower temperature range of 0.1 K or less. A 'reversing' melting in the paraffin was detected by TMDSC and the previously proposed integral ana lysis is found to be a useful tool for quantitative analysis of the thermal transition. Published by Elsevier Science B.V.