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ASLF/PVAc blends Table 1 Glass transition temperatures of PVAc and ASLF/PVAc blends
area of glasses applications. This can be realized in terms of the glass transition temperature ( T g ) and activation energy of glass transition ( E g ). Such activation energy is involved in the molecular motion and rearrangements of the atoms around
were measured at heating rate of 10 °C min −1 under the N 2 atmosphere over the scanning range of 35–500 °C. Samples of about 10–20 mg were cut into small pieces of 1 mm 3 were used for TG analysis. Both glass transition temperatures ( T g ) and the
published in [ 15 ], while kinetics and mechanism of crystallization of ZnO–B 2 O 3 –P 2 O 5 glasses was studied in [ 16 ]. It was found that that the replacement of P 2 O 5 by B 2 O 3 leads to an increase of glass transition temperature and dilatation
.613 Thermal curing The thermally curable samples were cured at different heating rates (2, 5, 7.5, 10, and 15 °C min −1 ) with a Mettler DSC-822e calorimeter from 0 °C to 250 °C. The ultimate glass transition temperature of the cured materials ( T g
with the results of Se 95 S 5 are shown in Fig. 1a . All glasses exhibit endothermic slope change because of the glass transition followed by exothermic crystallization peak. The observed glass transition temperatures ( T g ), the onset
activation energy. Differential scanning calorimeter (DSC) measurement shows that the amorphous Mg 61 Cu 24 Y 15 alloy exhibits distinct glass transition temperature and a wide supercooled liquid region before crystallization. Thus, the melt-spun Mg 61 Cu 24
thermal stability of the glasses. Most of these methods are based on characteristic temperatures, such as the glass transition temperature, T g , the onset crystallization temperature, T c , and the peak crystallization temperature, T p . The first
to the glass transition temperature T g of the fully cured network. During cure the T g is increasing until it reaches the highest possible glass transition temperature which is the glass transition temperature of the fully cured network ( T g
same heating rate. During DSC scanning, melting temperature ( T m ), melting enthalpy (Δ H m ), glass transition temperature ( T g ), and crystallization temperature ( T c ) were measured. The crystallinity was calculated by 1 2 Δ H PHB o
