Dynamic Mechanical Analysis (DMA) is a thermal analysis technique used to measure
changes in the viscoelastic response of a material as a function of temperature,
time, or deformation frequency. DMA is commonly used to determine quantitative
flexural storage and loss moduli, shear storage and loss moduli, tan delta, and
the dynamic and complex viscosity of materials. DMA is also particularly useful
for qualitatively characterizing the glass transition temperature and other sub-Tg
transitions of polymer and composite materials. A simplified explanation of the
DMA technique may be described as follows. Typically, a sample is clamped into the
DMA apparatus and subjected to an oscillatory deformation while being heated or
cooled at some controlled rate. The resonant frequency of the sample and
mechanical clamp assembly is continuously monitored as a function of temperature.
As the viscoelastic response of the material changes over some temperature range,
the electrical energy required to maintain a constant level of sample deformation
also changes and is continuously monitored. Quantitative analysis routines are
used to calculate the modulus (stiffness) and viscoelastic loss characteristics of
a specimen as a function of temperature or time. Transition temperatures are
readily obtained by determining the peak temperatures of the loss moduli or tan
delta profiles.
Examples
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Block copolymer samples generally exhibit at least two distinct material phases.
Since the mechanical loss characteristics of a material are directly related to
molecular level motions, the DMA damping signal is particularly sensitive to a
material's glass transition process. DMA loss profiles obtained on block
copolymers generally show two distinct Tgs, which are related to the Tgs of the
respective homopolymer components in the block copolymer, provided the inherent
component material transitions are sufficiently well separated.
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Determining the glass transition temperature and the flexural storage and loss
moduli of composite materials is a common DMA application. Composite samples
exhibit dramatic changes in their damping (loss) profiles and display
characteristic peaks as they pass through the glass transition temperature
range. Modulus data for composite materials are obtained by subjecting test
specimens to low strain displacements and then recording the corresponding
sample response to such deformations.