Thermomechanical Analysis (TMA) is used to characterize physical properties of materials when force is applied at specified temperatures and time periods. TMA is useful for investigating properties of viscoelastic materials, such as organic polymers. These materials exhibit both viscous and elastic properties that affect their response to mechanical stresses. For example, under conditions of ramping temperature under a fixed load, the viscoelastic material can exhibit changes in volume that correlate with changes in properties such as shrinkage, expansion, swelling and softening.
Measurements are performed by a probe that applies force to the sample. Before the test conditions are applied, the sample length is measured under a light force, which is used as the initial length (l0). As linear displacement occurs as a function of changing the applied force or temperature. The change in sample length (dl) is measured by an electrical transformer called an LVDT (linear variable displacement transducer). An example application is monitoring length change as the sample is slowly heated. In this case, the observance of a dramatic change in sample length can indicate a phase change, such as a glass transition (Tg), and the temperature at which Tg occurs can be calculated from the plot of length change versus temperature.
Thermomechanical Analysis techniques involve selection of an appropriate probe type for measuring the properties of interest: melting point, softening point, glass transition, contraction (shrinkage) and expansion coefficient (CTE). Probe/technique selection is based on the category of loading best suited to the sample type and the property measurements of interest. These categories are:
Compression Force
Measures: expansion and contraction of sample
Measures: penetration of sample
Tension Force
Works for films or fibers only
Measures: expansion and contraction of sample
Either Compression or Tension Force
Force ramp or step force to evaluate changing load on dimension change
Isostrain: Measures the amount of force required to maintain strain at a specified constant value while material is heated
Ideal Uses of TMA
Measuring glass transition temperature (Tg) of polymers
Coefficient of thermal expansion (CTE) of polymers, composites or inorganics
Differences in CTE below and above Tg
Differences in softening temperature before and after processing or physical aging
Effect of post-curing on the glass transition temperature
Dimensional stability of parts at operating temperature and loading
Differences in thermomechanical behavior of films or layered composites as a function of loading direction: “machine” and “transverse” or “in-plane” and “out-of-plane”
Shrinkage of oriented films
Strengths
Small sample size
Low force range
Force alteration: linear and stepwise
Programmable temperature: (1) sequential heating and cooling cycles, (2) isothermal
Limitations
Bulk sample size range:
0.5 mm up to 26 mm (z-axis, i.e. height or thickness)
Parallel faces for expansion
Reasonably flat for penetration
5 mm up to 10 mm (x -and y-dimension, i.e. width and length)
Film/Fibers size range
Maximum sample thickness (uniform) = 1 mm
TMA Technical Specifications
Temperature Operation: -150-1,000° C
Temperature Ramp: 1-20°C/minute
Force Range: 0.001 to 2 N (204 g)
Operating Mode: Standard
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