Melting crystallization temperature

Fig. 2.18. Schematic DSC thermogram of a semicrystalline polymer = glass transition temperature = crystallization temperature = melting temperature = decomposition temperature...

DSC is a thermal analysis technique that is used to measure the temperatures and energy flows related to transitions in materials as a function of time and temperature.These measurements provide qualitative and quantitative information about physical and chemical changes that involve endothermic or exothermic processes or changes in heat capacity. Any event, such as loss of solvent, phase transitions, crystallization temperature, melting point, and degradation temperature of the plastic sample, result in a change in the temperature of the sample. The systems available cover a wide temperature range, e g., -60°Cto>l,500°C. 

Figure 8.9. Estimation of the equilibrium melting point (by extr olation of crystallization temperature-melting point data.

Tsuji (2002) conducted an investigation into the hydrolysis of an amorphous form of PLA, to determine the effects of L-lactide content, tacticity and enantiomeric polymer blends. In this work four samples were prepared—poly(D,L-lactide), poly(L-lactide), poly(D-lactide) film and the blend sample of poly(L-lactide) and poly(D-lactide). The results are sununa-rized in Table 7.4, which also covers a complementary study that explored the effects of hydrolysis in terms of molecular weight and its distribution, glass transition temperature, crystallization temperature, melting temperature and mechanical properties. 

Valov P M and Leiman V I 1997 Size effects in the melting and crystallization temperatures of copper chloride nanocrystals in glass JETP Lett. 66 510... 

The normal boiling point of 2-methylthiazole is 17 0= 128.488 0.005°C. The purity of various thiazoles was determined cryometrically by Handley et al. (292), who measured the precise melting point of thiazole and its monomethyl derivatives. Meyer et al. (293, 294) extended this study and, from the experimental diagrams of crystallization (temperature/degree of crystallization), obtained the true temperatures of crystallization and molar enthalpies of fusion of ideally pure thiazoles (Table 1-43). 

The lower the crystallization temperature, the lower the melting point. 

Melting occurs over a range of temperatures, as in Fig. 4.1. The range narrows as the crystallization temperature increases. This is probably due to a wider range of crystal dimensions and less perfect crystals under the lower temperatures of formation. 

To erase information by the transition amorphous — crystalline, the amorphous phase of the selected area must be crystallized by annealing. This is effected by illumination with a low power laser beam (6—15 mW, compared to 15—50 mW for writing/melting), thus crystallizing the area. This crystallization temperature is above the glass-transition point, but below the melting point of the material concerned (Eig. 15, Erase). 

Other crystallization parameters have been determined for some of the polymers. The dependence of the melting temperature on the crystallization temperature for the orthorhombic form of POX (T = 323K) and both monoclinic (T = 348K) and orthorhombic (T = 329K) modifications of PDMOX has been determined (284). The enthalpy of fusion, Aff, for the same polymers has been determined by the polymer diluent method and by calorimetry at different levels of crystallinity (284). for POX was found to be 150.9 J/g (36.1 cal/g) for the dimethyl derivative, it ranged from 85.6 to 107.0 J/g (20.5—25.6 cal/g). Numerous crystal stmcture studies have been made (285—292). Isothermal crystallization rates of POX from the melt have been determined from 19 to —50 C (293,294). Similar studies have been made for PDMOX from 22 to 44°C (295,296). 

Fig. 4. Relation between crystallization temperature and melting temperature for natural mbber.

The variation of the transition temperatures of these polybibenzoates with the number of methylene units in the spacer is shown in the lower part of Fig. 5. Melting temperatures, Tm, (crystal-isotropic melt transition) are obtained [9] for m > 7 and m = 3 (monotropic behavior), while for the other members, Tm really represents the... 

Atomic number Atomic weight Crystal structure Melting Density Thermal Electrical resistivity (at 20°C) Temperature coefficient of resistivity Specific Thermal Standard electrode potential Thermal neutron absorption cross-section. 

The change in Gibbs free energy, AG, in the formation of FCC and ECC, depending on the drawing ratio of the melt ft and the crystallization temperature, is given by14 ... 

Figure 4 (curve 1) shows that in the absence of extension the distribution function W(fi) lies in the range 0 < /S < 0.2 for relatively long chains. In other words, in the absence of external forces, crystallization of flexible-chain polymers always proceeds with the formation of FCC since in the unperturbed melt the values of /3 are lower than /3cr. For short chains, the function W(/3) is broader (at the same structural flexibility f) (Fig. 4, curve 2) and the chains are characterized by the values of > /3cr, i.e. they can crystallize with the formation of ECC. Hence, at the same crystallization temperature, a... 

Fig. 13. Phase topogram. Curves 1 and 2-melting temperatures of FCC and ECC as a function of the degree of extension / curve 3 - dependence /4, on crystallization temperature. Arrows show the way of orientational crystallization ...

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