Dynamic mechanical thermal

Dynamic Mechanical Thermal Analyzer (DMTA) c 10-" -2 X 10" 10 -10" Rheometric Scientific, Inc., Piscataway, N.J. 

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). 

Dynamic mechanical thermal analysis has become a powerful tool for the assessment of cure and the study of the effect of extent of sure on film properties and performance (133,134). 

Continued speculation exists about the exact interaction of the MQ tackifier with the polysiloxane gum. Dynamic mechanical thermal analysis of a typical silicone PSA commonly shows two major transitions a Tg at low temperatures close to that of the pure gum, and a second T at higher temperature. Increasing tackifier loadings have little effect on the first transition but, as shown in Fig. 15, they shift the second transition to increasingly higher temperature [111]. By using... 

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... 

Figure 6 Typical plots from dynamic mechanical thermal analysis showing storage modulus and tan6 variation with temperature [27]. SO (---), S2 (--).

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. 

Jha A. and Bhowmick A.K., Thermoplastic elastomeric blends of nylon 6/acrylate rubber Influence of interaction of mechanical and dynamic mechanical thermal properties. Rubber Chem. TechnoL, 70, 798, 1997. 

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... 

DMTA dynamic mechanical thermal analysis DOP dioctyl phthalate... 

An apparatus for measuring the dynamic modulus and hysteresis of elastomers. The stress-strain oscillogram is shown on a ground-glass screen by means of an optical system. Now superseded by modem computer controlled servo hydraulic and dynamic mechanical thermal analysis machines. Roll Bending... 

An instrument designed to follow hysteresis losses in polymers by measuring the resistance to the rolling of small balls over the surface of the test piece it can investigate transitions in polymers to as low a temperature as -120 °C. Superseded by modem dynamic mechanical thermal analysis equipment. 

Recently, Kroeze et al. prepared polymeric iniferter 34 including poly(BD) segments in the main chain [152]. They successfully synthesized poly(BD)-block-poly(SAN), which was characterized by gel permeation chromatography, elemental analysis, thermogravimetric analysis, NMR, dynamic mechanical thermal analysis, and transmission electron microscopy. By varying the polymerization time and iniferter concentration, the composition and the sequence length were controlled. The analysis confirmed the chain microphase separation in the multiblock copolymers. 

Luck, W.A.P. 1981. Structures of water in aqueous systems. In Water Activity Influences on Food Quality (L.B. Rockland and G.F. Stewart, eds), pp. 407 134. Academic Press, New York. Ludescher, R.D., Shah, N.K., McCaul, C.P., and Simon, K.V. 2001. Beyond Tg Optical luminescence measurements of molecular mobility in amorphous solid foods. Food Hydro colloids 15, 331-339. Ludwig, R. 2001. Water From cluster to the bulk. Angewandte Chem. Int. Ed. 40, 1808-1827. Maclnnes, W.M. 1993. Dynamic mechanical thermal analysis of sucrose solutions. In The Glassy State in Foods (J.M.V. Blanshard and PJ. Lillford, eds), pp. 223-248. Nottingham Univ. Press, Loughborough, Leicestershire. 

Dough Moulding Compound Dynamic Mechanical Thermal Analysis Direct Resin Injection and Venting Differential Scanning Calorimeter Differential Thermal Analysis Elongation at Break... 

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... 

The dynamic mechanical properties were studied via a Polymer Laboratories Dynamic Mechanical Thermal Analyzer (DMTA) used with ... 

The dynamic mechanical thermal analysis also indicated molecular mixing of the two components. The Tg of the thermoplastic was lower than the composite, as determined from the inflection point of the E curve seen in Figures 13 1. The PEOX glass transition temperature appeared at 62°C, while that for PVP showed up at ll5°C. The discrepancy in the Tg of PVP had already been addressed. The Tg extrapolated from the DMTA thermogram was reported since no artifacts were to be introduced. The samples exemplified for all DMTA thermograms were processed in a normalized fashion. Any thermal or hygroscopic Influences were eliminated. Some water may be trapped in the neat thermoplastics but this was minimized since they are hot pressed at 150°C and stored under calcium... 

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). 

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