The thermal properties of starch samples were performed using a differential scanning calorimeter (200 F3, Netzsch, Germany) equipped with a thermal analysis data station. The sample preparation and heating procedures were as described in Wang and Copeland.31 A starch sample (3 mg, dry base) was weighed into an aluminum pan, and then distilled water was added to obtain a sample:water ratio of 1:3 (w/w). The sample pan was sealed, equilibrated at room temperature for 12 h, and scanned from 20 to 100 °C at a heating rate of 10 °C/min. An empty pan was used as the reference. The onset temperatures (To), peak temperatures (Tp), conclusion temperatures (Tc), and melting enthalpy (ΔH) were calculated using Proteus analysis software.
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