Stress relaxation energy

Another resonant frequency instmment is the TA Instmments dynamic mechanical analy2er (DMA). A bar-like specimen is clamped between two pivoted arms and sinusoidally oscillated at its resonant frequency with an ampHtude selected by the operator. An amount of energy equal to that dissipated by the specimen is added on each cycle to maintain a constant ampHtude. The flexural modulus, E is calculated from the resonant frequency, and the makeup energy represents a damping function, which can be related to the loss modulus, E". A newer version of this instmment, the TA Instmments 983 DMA, can also make measurements at fixed frequencies as weU as creep and stress—relaxation measurements. 

It has often been pointed out for a long time that the hysteresis energy given from the hysteresis loop under large extension is too big compared with the viscoelastic dissipation energy. For example, the hysteresis loop given from the stress relaxation is only 20%-30% of that from the stress-strain curve, when both measurements are performed at the same relaxation time and the... 

A8. The Helmholtz elastic free energy relation of the composite network contains a separate term for each of the two networks as in eq. 5. However, the precise mathematical form of the strain dependence is not critical at small deformations. Although all the assumptions seem to be reasonably fulfilled, a simpler method, which would require fewer assumptions, would obviously be desirable. A simpler method can be used if we just want to compare the equilibrium contribution from chain engangling in the cross-linked polymer to the stress-relaxation modulus of the uncross-linked polymer. The new method is described in Part 3. 

In a further development of the continuous chain model it has been shown that the viscoelastic and plastic behaviour, as manifested by the yielding phenomenon, creep and stress relaxation, can be satisfactorily described by the Eyring reduced time (ERT) model [10]. Creep in polymer fibres is brought about by the time-dependent shear deformation, resulting in a mutual displacement of adjacent chains [7-10]. As will be shown in Sect. 4, this process can be described by activated shear transitions with a distribution of activation energies. The ERT model will be used to derive the relationship that describes the strength of a polymer fibre as a function of the time and the temperature. 

The spring is elastically storing energy. With time this energy is dissipated by flow within the dashpot. An experiment performed using the application of rapid stress in which the stress is monitored with time is called a stress relaxation experiment. For a single Maxwell model we require only two of the three model parameters to describe the decay of stress with time. These three parameters are the elastic modulus G, the viscosity r and the relaxation time rm. The exponential decay described in Equation (4.16) represents a linear response. As the strain is increased past a critical value this simple decay is lost. 

The large scale molecular motions which take place in the rubber plateau and terminal zones of an uncross-linked linear polymer give rise to stress relaxation and thereby energy dissipation. For narrow molecular weight distribution elastomers non-catastrophic rupture of the material is caused by the disentanglement processes which occur in the terminal zone, e.g., by the reptation process. In practical terms it means that the green strength of the elastomer is poor. 

Annealing in metals can first lead to stress relaxation in which stored internal strain energy due to plastic deformation is relieved by thermally activated dislocation motion (see Figure 5.18). Because there is enhanced atomic mobility at elevated temperatures, dislocation density can decrease during the recovery process. At still higher temperatures, a process known as recrystallization is possible, in which a new set of... 

Work in groups of three. The shift factor, or, in the WLF Equation [Eq. (5.76)], is actually a ratio of stress relaxation times, f , in the polymer at an elevated temperature, T, relative to some reference temperature. To, and can be related via an Arrhenius-type expression to the activation energy for relaxation, Erei as... 

The shape of the creep and recoil curves provide insight about the sample, as does the stress relaxation response. A very strongly curved retardation response resembling a square wave is indicative of dominantly elastic behavior. A stress relaxation response for an elastic solid gives an almost horizontal line with very little decay, because almost all the energy is stored. A creep recoil curve that almost returns to the initial state of zero compliance is indicative of a very elastic system, because stored energy is almost completely recovered. 

A linear output is associated with a liquidlike or viscous response. The retardation response of a Newtonian liquid is a straight line through the origin, where the slope of the line is inversely proportional to the viscosity. A stress relaxation response for a Newtonian liquid is a narrow spike, as energy is dissipated very quickly. Typically the recoil part of a creep curve will be almost horizontal if there is little elasticity in the sample. 

The mechanical properties of Shell Kraton 102 were determined in tensile creep and stress relaxation. Below 15°C the temperature dependence is described by a WLF equation. Here the polystyrene domains act as inert filler. Above 15°C the temperature dependence reflects added contributions from the polystyrene domains. The shift factors, after the WLF contribution, obeyed Arrhenius equations (AHa = 35 and 39 kcal/mole). From plots of the creep data shifted according to the WLF equation, the added compliance could be obtained and its temperature dependence determined independently. It obeyed an Arrhenius equation ( AHa = 37 kcal/mole). Plots of the compliances derived from the relaxation measurements after conversion to creep data gave the same activation energy. Thus, the compliances are additive in determining the mechanical behavior. 

The stress in c-BN layers caused by the high energetic ions is a problem, because many of the nano-cBN coatings delaminate during or immediately after deposition. Several investigations have showed ways to reduce the stress in the layers (e.g. buffer layers [205, 217, 236], regulation of the ion energy [207], or ion-induced stress relaxation [206]). 

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