Viscoelastic properties temperature dependence

The radiation and temperature dependent mechanical properties of viscoelastic materials (modulus and loss) are of great interest throughout the plastics, polymer, and rubber from initial design to routine production. There are a number of laboratory research instruments are available to determine these properties. All these hardness tests conducted on polymeric materials involve the penetration of the sample under consideration by loaded spheres or other geometric shapes [1]. Most of these tests are to some extent arbitrary because the penetration of an indenter into viscoelastic material increases with time. For example, standard durometer test (the "Shore A") is widely used to measure the static "hardness" or resistance to indentation. However, it does not measure basic material properties, and its results depend on the specimen geometry (it is difficult to make available the identity of the initial position of the devices on cylinder or spherical surfaces while measuring) and test conditions, and some arbitrary time must be selected to compare different materials. 

For a fiber immersed in water, the ratio of the slopes of the stress—strain curve in these three regions is about 100 1 10. Whereas the apparent modulus of the fiber in the preyield region is both time- and water-dependent, the equiUbrium modulus (1.4 GPa) is independent of water content and corresponds to the modulus of the crystalline phase (32). The time-, temperature-, and water-dependence can be attributed to the viscoelastic properties of the matrix phase. 

The viscoelastic nature of the matrix in many fibre reinforced plastics causes their properties to be time and temperature dependent. Under a constant stress they exhibit creep which will be more pronounced as the temperature increases. However, since fibres exhibit negligible creep, the time dependence of the properties of fibre reinforced plastics is very much less than that for the unreinforced matrix. 

In a fundamental sense, the miscibility, adhesion, interfacial energies, and morphology developed are all thermodynamically interrelated in a complex way to the interaction forces between the polymers. Miscibility of a polymer blend containing two polymers depends on the mutual solubility of the polymeric components. The blend is termed compatible when the solubility parameter of the two components are close to each other and show a single-phase transition temperature. However, most polymer pairs tend to be immiscible due to differences in their viscoelastic properties, surface-tensions, and intermolecular interactions. According to the terminology, the polymer pairs are incompatible and show separate glass transitions. For many purposes, miscibility in polymer blends is neither required nor de-... 

When an engineering plastic is used with the structural foam process, the material produced exhibits behavior that is easily predictable over a large range of temperatures. Its stress-strain curve shows a significantly linearly elastic region like other Hookean materials, up to its proportional limit. However, since thermoplastics are viscoelastic in nature, their properties are dependent on time, temperature, and the strain rate. The ratio of stress and strain is linear at low strain levels of 1 to 2%, and standard elastic design... 

The time/temperature-dependent change in mechanical properties results from stress relaxation and other viscoelastic phenomena that are typical of these plastics. When the change is an unwanted limitation it is called creep. When the change is skillfully adapted to use in the overall design, it is referred to as plastic memory. 

Viscoelasticity A combination of viscous and elastic properties in a plastic with the relative contribution of each being dependent on time, temperature, stress, and strain rate. It relates to the mechanical behavior of plastics in which there is a time and temperature dependent relationship between stress and strain. A material having this property is considered to combine the features of a perfectly elastic solid and a perfect fluid. 

Dynamic mechanical measurements for elastomers that cover wide ranges of frequency and temperature are rather scarce. Payne and Scott [12] carried out extensive measurements of /a and /x" for unvulcanized natural mbber as a function of test frequency (Figure 1.8). He showed that the experimental relations at different temperatures could be superposed to yield master curves, as shown in Figure 1.9, using the WLF frequency-temperature equivalence, Equation 1.11. The same shift factors, log Ox. were used for both experimental quantities, /x and /x". Successful superposition in both cases confirms that the dependence of the viscoelastic properties of rubber on frequency and temperature arises from changes in the rate of Brownian motion of molecular segments with temperature. 

Investigation of the linear viscoelastic properties of SDIBS with branch MWs exceeding the critical entanglement MW of PIB (about -7000 g/mol ) revealed that both the viscosity and the length of the entanglement plateau scaled with B rather than with the length of the branches, a distinctively different behavior than that of star-branched PIBs. However, the magnitude of the plateau modulus and the temperature dependence of the terminal zone shift factors were found to... 

The understanding of the temperature and conversion dependence of the crosslinking kinetics is one of the prerequisites for understanding the changes in viscosity and viscoelastic properties as a function of reaction time and reaction temperature ( ). Three main factors determine these relations the reaction kinetics determined by temperature and conversion, the changes in structure determined primarily by conversion and the changes in Tg determined primarily also by conversion. 

The time and temperature dependent properties of crosslinked polymers including epoxy resins (1-3) and rubber networks (4-7) have been studied in the past. Crosslinking has a strong effect on the glass transition temperature (Tg), on viscoelastic response, and on plastic deformation. Although experimental observations and empirical expressions have been made and proposed, respectively, progress has been slow in understanding the nonequilibrium mechanisms responsible for the time dependent behavior. 

Polymers are viscoelastic materials meaning they can act as liquids, the visco portion, and as solids, the elastic portion. Descriptions of the viscoelastic properties of materials generally falls within the area called rheology. Determination of the viscoelastic behavior of materials generally occurs through stress-strain and related measurements. Whether a material behaves as a viscous or elastic material depends on temperature, the particular polymer and its prior treatment, polymer structure, and the particular measurement or conditions applied to the material. The particular property demonstrated by a material under given conditions allows polymers to act as solid or viscous liquids, as plastics, elastomers, or fibers, etc. This chapter deals with the viscoelastic properties of polymers. 

When a polymer is used as a structural material, it is important that it be capable of withstanding applied stresses and resultant strains over its useful service life. Polymers are viscoelastic materials, having the properties of solids and viscous liquids. These properties are time- and temperature-dependent. 

Figure 5. Temperature dependence of viscoelastic property of ozonized lignin/epoxy resins cured with hexamethylenediamine. Ozonized lignin content in DGEBA (1) 0 PHR (2) 20 PHR (3) 40 PHR (4) 80 PHR.

Although most physical properties (e.g., viscosity, density, heat conductivity and capacity, and surface tension) must be regarded as variable, it is of particular value that viscosity can be varied by many orders of magnitude under certain process conditions (5,11). In the following, dimensional analysis will be applied exemplarily to describe the temperature dependency of the viscosity and the viscosity of non-Newtonian fluids (pseudoplastic and viscoelastic, respectively) as influenced by the shear stress. 

The dynamic mechanical thermal analyzer (DMTA) is an important tool for studying the structure-property relationships in polymer nanocomposites. DMTA essentially probes the relaxations in polymers, thereby providing a method to understand the mechanical behavior and the molecular structure of these materials under various conditions of stress and temperature. The dynamics of polymer chain relaxation or molecular mobility of polymer main chains and side chains is one of the factors that determine the viscoelastic properties of polymeric macromolecules. The temperature dependence of molecular mobility is characterized by different transitions in which a certain mode of chain motion occurs. A reduction of the tan 8 peak height, a shift of the peak position to higher temperatures, an extra hump or peak in the tan 8 curve above the glass transition temperature (Tg), and a relatively high value of the storage modulus often are reported in support of the dispersion process of the layered silicate. 

The viscoelastic properties are highly temperature-dependent so that the maximum temperature should be always specified and taken into account. Polymers at room temperature behave by different ways i.e. hard solids, elastic liquids, rubbers, etc [1,7]. 

The viscoelastic response of polymer melts, that is, Eq. 3.1-19 or 3.1-20, become nonlinear beyond a level of strain y0, specific to their macromolecular structure and the temperature used. Beyond this strain limit of linear viscoelastic response, if, if, and rj become functions of the applied strain. In other words, although the applied deformations are cyclic, large amplitudes take the macromolecular, coiled, and entangled structure far away from equilibrium. In the linear viscoelastic range, on the other hand, the frequency (and temperature) dependence of if, rf, and rj is indicative of the specific macromolecular structure, responding to only small perturbations away from equilibrium. Thus, these dynamic rheological properties, as well as the commonly used dynamic moduli... 

With viscoelastic models used by an increasing number of researchers, time and temperature dependence, as well as strain hardening and nonisotropic properties of the deformed parison can, in principle, be accounted for. Kouba and Vlachopoulos (97) used the K-BKZ viscoelastic constitutive equation to model both thermoforming and parison membrane stretching using two-dimensional plate elements in three-dimensional space. Debbaut et al. (98,99) performed nonisothermal simulations using the Giesekus constitutive equation. 

To quantify the abnormal viscoelastic properties of PFPE due to the polar endgroup, we conducted oscillatory experiments at different temperatures. We found that G" is strongly dependent on temperature, while G is weakly dependent on temperature. Figure 1.17 shows the behavior of the dynamic moduli at different temperatures. 

Thixotropy is the tendency of certain substances to flow under external stimuli (e.g., mild vibrations). A more general property is viscoelasticity, a time-dependent transition from elastic to viscous behavior, characterized by a relaxation time. When the transition is confined to small regions within the bulk of a solid, the substance is said to creep. A substance which creeps is one that stretches at a time-dependent rate when subjected to constant stress and temperature. The approximately constant stretching rates at intermediate times are used to characterize the creeping characteristics of the material. 

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