Mechanical Thermal Analysis DMTA

The temperature range of the DMTA is from -150°C to 300°C and frequencies from 0.033 to 90 Hz. The sample size for the usual flexural test mode is 1 mm x 10 mm x 40 mm slightly less sample is required in the parallel plate shear mode. 

MAXIMUM TEMPERATURES TO WHICH STORAGE MODULUS (log E) VALUE OF THE CROSSLINKED POLYURETHANE ELASTOMER WILL REMAIN CONSTANT  

---

Similar information can be obtained from analysis by dynamic mechanical thermal analysis (dmta). Dmta measures the deformation of a material in response to vibrational forces. The dynamic modulus, the loss modulus, and a mechanical damping are deterrnined from such measurements. Detailed information on the theory of dmta is given (128). 

Viscoelastic phenomena always involve the change of properties with time and, therefore, the measurements of viscoelastic properties of solid polymers may be called dynamic mechanical. Dynamic mechanical thermal analysis (DMTA) is a very useful tool for studying... 

The relaxation methods employed are Dynamic Mechanical Thermal Analysis (DMTA) and Dielectric Thermal Analysis (DETA). Generally in both cases a single excitation frequency is used and the temperature is varied,... 

This second group of tests is designed to measure the mechanical response of a substance to applied vibrational loads or strains. Both temperature and frequency can be varied, and thus contribute to the information that these tests can provide. There are a number of such tests, of which the major ones are probably the torsion pendulum and dynamic mechanical thermal analysis (DMTA). The underlying principles of these dynamic tests have been covered earlier. Such tests are used as relatively rapid methods of characterisation and evaluation of viscoelastic polymers, including the measurement of T, the study of the curing characteristics of thermosets, and the study of polymer blends and their compatibility. They can be used in essentially non-destructive modes and, unlike the majority of measurements made in non-dynamic tests, they yield data on continuous properties of polymeric materials, rather than discontinuous ones, as are any of the types of strength which are measured routinely. 

Differential Scanning Calorimeter (DSC) thermograms were obtained on a Perkin Elmer DSC-2 run at 10°C per minutes. Dynamic Mechanical Thermal Analysis (DMTA) spectra were obtained on a Polymer Labs DMTA at a frequency of 1Hz with a temperature range from -150°C to +150°C at a scan rate of 5°C per minute. 

The physical properties of the acid- and ion-containing polymers are quite interesting. The storage moduli vs. temperature behavior (Figure 8) was determined by dynamic mechanical thermal analysis (DMTA) for the PS-PIBMA diblock precursor, the polystyrene diblock ionomer and the poly(styrene)-b-poly(isobutyl methacrylate-co-methacrylic acid) diblock. The last two samples were obtained by the KC>2 hydrolysis approach. It is important to note that these three curves are offset for clarity, i.e. the modulus of the precursor is not necessarily higher than the ionomer. In particular, one should note the same Tg of the polystyrene block before and after ionomer formation, and the extension of the rubbery plateau past 200°C. In contrast, flow occurred in... 

Polymer films of approximately 1000 microns wet film thickness were laid down with a bar applicator on PTFE coated glass panels and the solvent allowed to evaporate at ambient temperature for a standard period of seven days. A typical plot of solvent weight loss with time is shown in Figure 2. The thickness of the wet film was dictated by the need to have adequate mechanical strength in the dry films in order that they might be suitable for subsequent mechanical test procedures. Dry film thicknesses were approximately 300 microns as measured by micrometer. The dried polymer films were examined by dynamic mechanical thermal analysis (DMTA) (Polymer Laboratories Ltd.). Typical DMTA data for a polymer and paint are... 

Network formation by photopolymerization has been studied for tetraethyleneglycol diacrylate (TEGDA) using isothermal calorimetry (DSC), isothermal shrinkage measurement and dynamic mechanical thermal analysis (DMTA). Due to vitrification the polymerization does not go to completion at room temperature. The ultimate conversion as measured by DSC seems to depend on light intensity. This can be explained by the observed delay of shrinkage with respect to conversion. 

Since the polymerization of TEGDA can easily be studied with DSC as well as with dynamic mechanical thermal analysis (DMTA) we have repeated our study with this monomer in order to see whether or not mechanical properties depend on the intensity rather than on the dose of UV irradiation. DMTA also reveals whether or not postcuring occurs during thermal after-treatment, similar to what has been observed with other thermosetting materials (8). 

The styrene content affects the crystallinity of ESI (131) for >50% styrene the copolymers are amorphous. As the styrene content is increased from 50 to 70% styrene the Tg increases from -15 °C to 20 °C. Low density foams were made (8) from a blend of 50% of various ESI polymers, 33% of EVA and 17% of azodicarbonamide blowing agent. Thermal analysis showed that the blends, with an ESI having approximately 70% styrene, had a Tg in the range 22 to 30 °C. Dynamic mechanical thermal analysis (DMTA) traces (see Section 5.1) show that these blends... 

Dynamic mechanical thermal analysis (DMTA) Pendulum hardness... 

Dynamic mechanical analysis (DMA) or dynamic mechanical thermal analysis (DMTA) provides a method for determining elastic and loss moduli of polymers as a function of temperature, frequency or time, or both [1-13]. Viscoelasticity describes the time-dependent mechanical properties of polymers, which in limiting cases can behave as either elastic solids or viscous liquids (Fig. 23.2). Knowledge of the viscoelastic behavior of polymers and its relation to molecular structure is essential in the understanding of both processing and end-use properties. 

Most of the physical properties of the polymer (heat capacity, expansion coefficient, storage modulus, gas permeability, refractive index, etc.) undergo a discontinuous variation at the glass transition. The most frequently used methods to determine Tg are differential scanning calorimetry (DSC), thermomechanical analysis (TMA), and dynamic mechanical thermal analysis (DMTA). But several other techniques may be also employed, such as the measurement of the complex dielectric permittivity as a function of temperature. The shape of variation of corresponding properties is shown in Fig. 4.1. 

Faced with a lack of sensifivify of differential scanning calorimetry (DSC) for detecting a clear event assignable to the glass transition in low-density material, the powders were compressed for 5 min af 25°C into disk-shaped tabletted samples. For further DSC analysis, the tabletted samples were crushed into a coarse powder. For d)mamical mechanical thermal analysis (DMTA), the disks were cut into parallepiped shape (10 X 7 X 2 mm). Prior to their analysis, the samples were returned to the humidity-controlled atmospheres. 

---