Source: Danielle N. Beatty and Taylor D. Sparks, Department of Materials Science and Engineering, The University of Utah, Salt Lake City, UT
Differential scanning calorimetry (DSC) is an important measurement to characterize thermal properties of materials. DSC is used primarily to calculate the amount of heat stored in a material as it heats up (heat capacity) as well as the heat absorbed or released during chemical reactions or phase changes. However, measurement of this heat can also lead to the calculation of other important properties such as glassy transition temperature, polymer crystallinity, and more.
Due to the long, chain-like nature of polymers it is not uncommon for polymer strands to be entangled and disordered. As a result, most polymers are only partially crystalline with the remainder of the polymer being amorphous. In this experiment we will utilize DSC to determine polymer crystallinity.
Figure 3 shows the result of a DSC percent crystallinity sample scan on a polybutylene terephthalate (PBT) polymer sample. The result is displayed as a DSC power reading (in milliwatts per milligram of sample) verses time. The power reading, the blue trace in Figure 3, indicates how much additional power was required to change the temperature of the sample pan in comparison to the empty reference pan. The temperature program is a
Differential scanning calorimetry is a technique used to determine many thermal properties of materials, such as heat of melting, heat of crystallization, heat capacity, and phase changes. DSC measurements can also be used to calculate additional material properties including glassy transition temperature and polymer percent crystallinity. The DSC requires very small samples that must conform to the size and shape of the pans used in the machine and is based on a differential heat comparison between an empty reference an
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