2.13. Differential Scanning Calorimetry (DSC)

TH Tim Höhnemann
MS Mark Steinmann
SS Stefan Schindler
MH Martin Hoss
SK Simon König
AO Antje Ota
MD Martin Dauner
MB Michael R. Buchmeiser
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DSC (differential scanning calorimetry) measurements were carried out under air (20 mL·min−1) on a Q2000 differential scanning calorimeter (TA Instruments Inc., New Castle, DE, USA) while applying a heating rate of 10 K·min–1. The sample mass was 2 mg. The melt enthalpy ΔHm and melting peak temperature Tm,p were determined from the heat flow–temperature curves, as well as the glass-transition temperature Tg. One measurement per sample was carried out using the 1st heating cycle only, for both the granules and the fiber samples. This is because the second heating cycle gives no information on the history of the material and because the (re-)crystallization of PEF is very slow and therefore not displayable by DSC measurements.

The degree of crystallinity χc was calculated by standardizing the melt enthalpy to the standard melt enthalpy ΔHm,0, as shown by Equation (1).

The standard melt enthalpy ΔHm,0 used was 137 J·g−1 according to the literature [9].

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