Melting Point (Tf)
Laboratory > Thermal
Melting point (Tf) | ||
The fusion of the crystalline polymer occurs when the vibratory movements of the molecular segments of the crystalline cell around its middle positions reach this amplitude to overcome the cohesive forces existing in the cristilite: this becomes a more or less viscous liquid in which the macromolecules can move, rotate and vibrate and even assume or oscillate between infinite different conformations. In the case of the passage of an amorphous polymer from the glass to the plastic or rubber state, the segments of the molecule, previously located in fixed positions and with limited possibilities of movement, at the temperature Tg begin to acquire greater mobility and rotation of translation and As the temperature Sal, the movement becomes cooperative, that is, it extends to the entire chain and reaches enough energy to break the intermolecular bonds. The crystalline structure of a semicrystalline solid. | ||
Crystalline structure | ||
The crystalline structure of a solid semicrystalline polymer disappears at the melting point, Tm, when the material undergoes a phase change from solid to liquid. At the melting point, physical properties of the material, such as density, refractive index, heat capacity and transparency, change abruptly as the material becomes a viscous liquid. Melting points are commonly measured using differential scanning calorimetry (DSC). The melting points decrease dramatically with lower crystallinity. Polymers generally melt in a narrow temperature range instead of at a different point. In a resin with a particular crystallinity, variations in the lengths of the chains produce sheets of different thicknesses, which melt at slightly different temperatures. The melting point given for a polymer is generally the temperature at the highest point of the peak in a DSC scan. | ||
Differential scanning calorimetry (DSC) | ||
Differential scanning calorimetry (DSC) is a technique used to characterize the melting point and Tg of a crystalline polymer, based on the technique of measuring endothermic and exothermic transitions, such as the determination of transformation temperatures and enthalpy of solids and liquids as a function of temperature. It does this by measuring the heat change associated with the thermal denaturation of the polymer molecule when it is heated at a constant rate. All DSCs operate based on material analysis standards: ISO 113587, ASTM E968, ASTM E793, ASTM D3895, ASTM D3417, ASTM D3418, DIN 51004, DIN 51007 and DIN 53765 |