Covalent

Dynamic Mechanical Analysis (DMA)

Dynamic mechanical analysis (DMA) is a technique for characterizing the thermal and mechanical properties of soft materials like polymers.

What Is Dynamic Mechanical Analysis (DMA)?

DMA measures the displacement of the material under an applied force (periodic or constant).

Viscoelastic properties such as storage modulus, loss modulus, and tan delta are calculated by measuring the phase lag between the input applied periodic force and the resulting periodic displacement.

Examples of periodic/sinusoidal force include:

  • Viscoelastic material properties can be determined by DMA, such as storage and loss modulus, and tan delta.
  • Fatigue tests can be performed under continuous cyclic loading.
  • Under a controlled temperature range, the glass transition can be determined.
  • Oscillatory shear rheology.
  • Time-Temperature Superposition (TTS).

Examples of constant/quasi-static force include:

  • Compression-set of elastomers under continual force.
  • Creep/recovery.
  • Stress vs. strain of soft materials to determine Young’s modulus, ultimate tensile strength, etc.

Versatile Testing

Supports polymers, gels, and soft metals under tension, torsion, compression, and bending modes.

High Sensitivity

Detect subtle visoelastic changes, including storage modulus, loss modulus, and tan delta damping analysis.

Thermal Insight

Accurately measure glass transition temperature via DMA, with greater sensitivity than DSC.

Why Use DMA?

Dynamic Mechanical Analysis (DMA) is used to measure the bulk mechanical properties of viscoelastic solids, providing precise insights into their behavior under stress. It accommodates solid and gel-phase materials and operates over a typical displacement range from microns to millimeters, with forces ranging from 0.005 N to 50 N. This makes DMA an ideal technique for characterizing the viscoelastic performance of polymers, gels, and other soft materials across various testing conditions.

Polymer Analysis

Enables polymer DMA testing for bulk viscoelastic properties and long-term performance prediction.

Advanced Testing

Provides DMA frequency sweep testing and time–temperature superposition to evaluate material behavior.

Complementary Methods

Works alongside DSC and Instron to deliver complete viscoelastic property testing and reliability insights.

How Dynamic Mechanical Analysis Works

DMA works by applying an oscillatory force or stress to the sample and measuring the sample displacement or strain. Forces can be applied in tension/torsion, compression, and 3-point bend. The phase angle between the stress and strain oscillatory waves is calculated, which allows extrapolation of the storage and loss modulus.

ModeLength (mm)Width (mm)Thickness (mm)Temperature range (°C)Stiffness range (MPa)
Tension/Torsion5 to 355 to 150.01-5-100-3500.1-10000
Compression1 to 401 to 400.5-5-100-2200.0001-100
3-pt Bend45 to 5010 to 12stiff = 0.2-0.3
soft = 1-2
-100-350100 to 1000000

Force range: 0.005 N to 50 N.

Equipment Used for Nanoindentation

Anton Paar MCR 702 Multidrive (linear and rotation)

The MCR 702 MultiDrive is a combination DMA/rheometer with the flexibility and precision to support a wide range of test modes and configurations.
  • Platform: Combined DMA/rheometer supporting tension, bending, compression, torsion, and rheology modes.
  • Linear Drive: Force 0.5 mN–40 N; displacement 10 nm–9.4 mm; frequency 0.001–100 Hz.
  • Rotational Drive: Torque 0.5 nNm–230 mNm; angular frequency ~10⁻⁷–628 rad/s; normal force 0.005–50 N.
  • Temperature Range: −160 °C to +600 °C (linear) / up to +1000 °C (rotational, accessory-dependent).
  • Thermal Control: Max heating rate 35 K/min; max cooling rate 30 K/min.
Specifications

Key Differentiators

Strengths

  • Measures bulk viscoelastic properties such as storage and loss modulus.
  • More sensitive measurement of glass transition temperature compared to DSC.

Limitations

  • Not ideal for quasi-static tensile tests; the Instron with the 50N load cell is preferred.
  • Failure to properly grip or mount the sample during long measurement times can be problematic.
  • Coefficient of thermal expansion (CTE) is not well-suited for our tool.

Example Outputs

This graph shows results from the DMA master curve graph or hydrogel material at multiple frequencies.
This graph shows a curing study of silicone. The gel point indicates the transition from liquid to solid transition during the curing process.

Sample Requirements

DMA requires a solid form of samples of polymers, gels, and soft metals.

DMA by Industry

Polymers / Plastics / Elastomers

Used to measure glass transition temperature, stiffness, and damping to understand flexibility and performance across temperatures.

Composites & High-Performance Materials

Used to evaluate viscoelastic behavior and service temperature limits for fiber-reinforced and advanced materials.

Adhesives / Coatings / Films

Used to assess cured strength, flexibility, thermal stability, and high‑temperature viscoelastic behavior of adhesives, coatings, thin films, and semiconductor packaging materials (e.g. adhesives, epoxies, thermal interface materials, gels) to characterize flow behavior under load and at operating temperatures above their glass transition temperature (50 °C – 200 °C).

R&D & Quality Control

Used to compare formulations, validate processing, and ensure consistent mechanical and thermal performance.

Biomedical & Soft Materials

Used to characterize the viscoelastic properties and deformation behavior of soft tissues, gels, and biopolymers.

Techniques That Complement DMA

A universal testing machine like Covalent’s Instron can be used for standardized ASTM tensile tests, such as ASTM D638. This is a complementary technique to DMA for measuring Young’s tensile properties of plastics. Instron can achieve much higher forces compared to DMA (as high as 5kN).

Quantifies heat flow for material optimization.
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Measures material behavior under axial stretching (tension).
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Why Choose Covalent for Your DMA Needs?

At Covalent, we provide major advantages to utilizing DMA with our unique partnership agreement with Anton Paar to support customer projects, modules, and more. We can also schedule tests the same-day with advanced notice at the standard price.

Frequently Asked Questions

What properties can DMA measure, other than storage modulus, loss modulus, and tan delta?

DMA can also measure creep, compression-set, and glass transition temperature.

Are liquids suitable for DMA?

Gels are suitable in oscillatory shear mode. However, under linear drive, we require materials to be viscoelastic, meaning they have both viscous and elastic properties.

What sample size and geometry are required for DMA specimens?

Dynamic mechanical analysis (DMA) requires samples in solid form of polymers, gels, and soft metals. The specific specimen dimensions depend on the test mode. Typical ranges are: Tension/Torsion: length 5 to 35 mm, width 5 to 15 mm, thickness 0.01 to 5 mm Compression: length 1 to 40 mm, width 1 to 40 mm, thickness 0.5 to 5 mm 3‑point bend: length 45 to 50 mm, width 10 to 12 mm, thickness 0.2 to 0.3 mm for stiff samples and 1–2 mm for soft samples

What equipment configurations (force, temperature range) does Covalent use for DMA testing?

We typically perform an amplitude sweep at 1 Hz to determine the linear viscoelastic (LVE) range. This is the amplitude range at which the storage modulus is constant. Viscoelastic materials display frequency-dependent properties. If needed, we conduct frequency sweeps at an amplitude in the LVE. All tests are conducted at room temperature unless specified by the customer.

How long does a DMA test typically take? Are there expedited service options?

Tests can range from a few minutes to several hours, depending on the procedure. We understand that some tests are time-dependent. We can accommodate by scheduling same-day testing with one week’s advance notice.