Fig. 3.16 Differential scanning calorimetry data taken during heating of polyethylene, showing onset of melting at 112 °C (234 °F) and termination of melting at 138 °C (280 °F). Source: Barbosa et al. ( Ref 3 ) More

Fig. 3.19 Differential scanning calorimetry data used to measure heat capacity, in this case for a wax blend, showing a broad melting event. The integral of the curve is the basis for calculating the melting enthalpy. Source: Gebelin et al. ( Ref 4 ) More

Fig. 3.29 Differential scanning calorimetry curves for polypropylene and polypropylene mixed with added stearic acid up to 40 wt%. The heating rate was 5 °C/min (9 °F/min). The results show that stearic acid is soluble in polypropylene at low concentrations, but at 20%, the stearic acid forms More

Fig. 7.2 Differential scanning calorimetry curves More

Fig. 25 Differential scanning calorimetry thermogram More

Fig. 27 Differential scanning calorimetry (DSC) of polyethylene/polypropylene blend 10 mcal/s range; 20 °C/min (36 °F/min). PE, polyethylene; PP, polypropylene. Source: Ref 29 More

Fig. 5 Differential scanning calorimetry thermogram More

Fig. 6 Differential scanning calorimetry thermogram of polyethylene/polypropylene blend, 10 mcal/s range, 20 °C/min (36 °F/min) heating rate. PE, polyethylene; PP, polypropylene. Source: Ref 56 More

Fig. 7 Differential scanning calorimetry determination of the effect of a plasticizer on T m of nylon 11. Range, 0.0024 W (10 mcal/s); heating rate, 20 °C/min (36 °F/min); weight, 6.8 mg (0.105 gr), both samples. Source: Ref 51 More

Fig. 8 Differential scanning calorimetry determination of polyethylene in impact polycarbonate. Range, 0.00048 W (2 mcal/s); heating rate, 20 °C/min (36 °F/min); weight, 23 mg (0.355 gr). Source: Ref 51 More

Fig. 10 Differential scanning calorimetry thermogram of Fiberite 934 epoxy, 4.89 mg (0.075 gr), 10 °C/min (18 °F/min) heating rate More

Fig. 2 Annealing time effects on differential scanning calorimetry traces of epoxy 828-0-0. Annealed at 23 °C (73 °F). H , convective heat-transfer coefficient. Source: Ref 39 More

Fig. 15 Schematic differential scanning calorimetry thermogram More

Fig. 18 Differential scanning calorimetry of nylon gears. MW, molecular weight; T g , glass transition temperature; T m , melt temperature More

Fig. 19 Differential scanning calorimetry determination of the effect of a plasticizer on melting temperature ( T m ) of nylon 11. Range, 0.0024 W (10 mcal/s); heating rate, 20 °C/min (36 °F/min); weight, 6.8 mg (0.105 gr), both samples. Source: Ref 19 More

Fig. 20 Differential scanning calorimetry determination of polyethylene in impact polycarbonate. Range, 0.00048 W (2 mcal/s); heating rate, 20 °C/min (36 °F/min); weight, 23 mg (0.355 gr). T m , melting temperature; T g , glass transition temperature. Source: Ref 19 More

Fig. 5 Differential scanning calorimetry thermogram showing various transitions associated with polymeric materials. The (I) indicates that the numerical temperature was determined as the inflection point on the curve. More

Fig. 6 Differential scanning calorimetry used to identify polymeric materials by determination of their melting point More

Fig. 7 Differential scanning calorimetry used to detect glass transitions within amorphous thermoplastic resins. The (I) indicates that the numerical temperature was determined as the inflection point on the curve. More

Fig. 19 The differential scanning calorimetry thermogram representing the reference clip material, exhibiting an endothermic transition characteristic of the melting of a nylon 6/6 resin. The results also showed a second melting transition attributed to a hydrocarbon-based impact modifier. More