Differential scanning calorimetry DSC results

Worswick et al. [74WOR/COW] reported low-temperature (adiabatic calorimetry) heat capacity measurements (10 to 300 K) and differential scanning calorimetry (DSC) results from 300 to 550 K. The equation (V.66) (200 to 550 K) is not in the standard form generally used for solids e.g., [93KUB/ALC], p. 166, Equation (116)), however, the original DSC data are unavailable. 

FIGURE 3.4 Differential scanning calorimetry (DSC) result for pristine PEDOT-PSS (2920 modulated DSC TA instrument). 

The lamellar morphology formed in miscible blends is usually observed using SAXS as described in Section 10.2.2, because its typical repeating distance is in the order of 10nm. In addition, a combination of SAXS and differential scanning calorimetry (DSC) results straightforwardly provides the crystalline layer thickness and amorphous layer thickness if we assume a perfect lamellar morphology with no transition zone between both layers. 

In this chapter, microcellular foaming of low-Tg biodegradable and biocompatible polycaprolactone (PCL) in supercritical CO2 will be described. The effects of a series of variable factors, such as saturation temperature, saturation pressure, saturation time and depressurization time on the foam structures and density were studied through measurement of density and SEM observation. The experimental results show that higher saturation temperatures lead to a reduction in bulk densities and that different saturation pressures result in different nucleation processes. In addition, saturation time has a profound effect on the structure of the product. Both X-ray diffraction (XRD) and differential scanning calorimetry (DSC) results show that the foaming treatment widi supercritical CO2 increased the crystallinity of PCL. 

The process known as transimidization has been employed to functionalize polyimide oligomers, which were subsequentiy used to produce polyimide—titania hybrids (59). This technique resulted in the successhil synthesis of transparent hybrids composed of 18, 37, and 54% titania. The effect of metal alkoxide quantity, as well as the oligomer molecular weight and cure temperature, were evaluated using differential scanning calorimetry (dsc), thermogravimetric analysis (tga) and saxs. 

Differential scanning calorimetry (DSC) is fast, sensitive, simple, and only needs a small amount of a sample, therefore it is widely used to analyze the system. For example, a polyester-based TPU, 892024TPU, made in our lab, was blended with a commercial PVC resin in different ratios. The glass transition temperature (Tg) values of these systems were determined by DSC and the results are shown in Table 1. 

Structured proteins have also been investigated by thermal analysis [40,41], denaturing resulting in an endotherm which is readily detected by differential scanning calorimetry (DSC). DSC of recombinant resilin in the swollen state showed no transitions over a wide temperature range (25°C-140°C), further evidence of the absence of any strucmre. This is in contrast to the strucmred proteins wool and bovine serum albumin, which show denamration endotherms at 145°C and 62°C, respectively (Figure 9.6). 

Birefringence measurements have been shown to be very sensitive to bimodality, and have therefore also been used to characterize non-Gaussian effects resulting from it in PDMS bimodal elastomers [5,123]. The freezing points of solvents absorbed into bimodal networks are also of interest since solvent molecules constrained to small volumes form only relatively small crystallites upon crystallization, and therefore exhibit lower crystallization temperatures [124—126]. Some differential scanning calorimetry (DSC) measurements on... 

When one polymorph can be thermally converted to another, differential scanning calorimetry (DSC) analysis cannot be used to deduce the heat of transition between the two forms, and so solution calorimetry represents an alternative methodology. This situation was encountered when evaluating the polymorphs of losartan [140], Enthalpies of transition were obtained in water (A(A//sol) = 1.723 kcal/mol) and in A A-dimethylformarnide (A(A//S0 ) = 1.757 kcal/mol), with the equivalence in results demonstrating the quality of the results. Although enthalpy does not indicate stability, the authors deduced from solution calorimetry that form I was more stable than form II at ambient temperature. 

The results of differential scanning calorimetry(DSC) indicate the change in aggregation state. The trans micelle showed a main endothermic peak at 14 2°C(A H =1.0 kcal/mol), corresponding to a gel-liquid crystal phase transition, whereas the transition temperature for the cis micelle appeared at 11.9°C( AH = 0.8 kcal/mol). This is unequivocal evidence that the trans-cis photoisomerization is a sufficient perturbation to alter the state of molecular aggregation. 

Bisphthalonitrile monomers were cured neat, with nucleophilic and redox co-reactants, or in combination with a reactive diluent. Dynamic mechanical measurements on the resulting polymers from -150 to +300°C turn up several differences attributable to differences in network structure. Rheovibron results were supplemented with solvent extraction, differential scanning calorimetry (DSC), vapor pressure osmometry, and infrared spectroscopy to characterize the state of cure. 

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