Calorimetric measurements were carried out using a
Q2000 differential scanning calorimeter (DSC, TA Instruments, New Castle, DE, USA). Thermal analysis was carried out at a scanning rate of 20 °C/min. Samples (~3 mg) were heated to 200 °C and maintained for 5 min to erase previous thermal history before being cooled to −40 °C at a cooling rate of 20 °C/min. Samples were then reheated to 200 °C at a scanning rate of 20 °C/min (2nd heating) under nitrogen atmosphere using a nitrogen flow rate of 40 mL/min. Percentage crystallinity (X
c) of the synthesized polymer samples was determined using the following Equation (1):
where
is the melting enthalpy (J/g) of sample, w is the weight fraction of PHB in PU, and
is the melting enthalpy of 100% crystalline PHB (146 J/g) [13 (
link)].
Thermal degradation studies were carried out using TA Instruments D-TGA,
SDT 2960 thermal analyzer. Experiments were conducted in air atmosphere at heating scans from 30 to 600 °C under dynamic heating rate of 10 °C/min (sample amount: 3–5 mg).
Saha P., Khomlaem C., Aloui H, & Kim B.S. (2021). Biodegradable Polyurethanes Based on Castor Oil and Poly (3-hydroxybutyrate). Polymers, 13(9), 1387.