Range Of Low Deformations Research Articles

Investigation the Effect of MR Fluid Composition on Properties at Low Strain Ranges.

The paper presents the results of eight magnetorheological (MR) fluids of different compositions. Magnetite and carbonyl iron were used as magnetic particles. MR fluids based on glycerin and OKS 352 oil were produced using stabilizers in the form of oleic acid and Aerosil 200 (Evonik Resource Efficiency GmbH, Hanau, Germany) silica; additives such as graphite and yellow dextrin were also used. The aim of the study was to determine the properties of various combinations of components on the dynamic properties of MR fluids, i.e., properties characterizing the fluid within the range of low deformations, as well as to investigate the effect of different compositions on structural yield stress and flow stress prepared MR fluids at different magnetic field induction values.

Amorphous and Semicrystalline Blends of Poly(vinylidene fluoride) and Poly(methyl methacrylate): Characterization and Modeling of the Mechanical Behavior

After extensive studies starting in the 1970s in relation to miscibility and piezoelectric properties, the blends of poly(vinylidene fluoride) (PVDF) and poly(methyl methacrylate) (PMMA) have been revisited with the aim of assessing their mechanical behavior. Depending on the amount of PVDF, either amorphous or semicrystalline blends are produced. Typically, the blends remain amorphous when their PVDF content does not exceed 40 wt. %. Blend composition influence on the values of the glass transition temperature, Tg, and on its mechanical expression, Tα, is extensively discussed. Then, emphasis is put on the stress-strain behavior in tension and compression over the low deformation range covering the elastic, anelastic, and viscoplastic response. The reported data depend, as expected, on temperature and strain rate and also, markedly, on blend composition and degree of crystallinity. Molecular arguments, based on the contribution of the glass transition motions are proposed to account for the observed behavior. Thanks to the understanding of phenomena at the molecular level, accurate models can be selected in the view of mechanical modeling.

Thermal and mechanical behavior of amorphous and semi‐crystalline poly(vinylidene fluoride)/poly(methyl methacrylate) blends

AbstractVarious PVDF/PMMA (poly(vinylidene fluoride)/poly(methyl methacrylate)) blends were selected for mechanical testing in compression. At low PVDF content (less than 50/50 w/w), the blends remain amorphous and PVDF and PMMA are fully miscible. In PVDF‐richer blends, PVDF crystallizes in part, leading to a PMMA‐enriched homogeneous amorphous phase. In this study, the degree of crystallinity was set at equilibrium by appropriate annealing of the samples before testing. Mechanical analysis was focused on the low deformation range, and especially on the yield region. Depending on the test temperature and blend composition, three types of response were identified, depending on whether plastic deformation is influenced: 1) by the PMMA secondary relaxation motions, 2) by the PVDF/PMMA glass transition motions, or 3) by the crystallite‐constrained PVDF chains.

Polyurethane network structure from tensile tests

AbstractThe mechanical behavior of polyurethane networks based on polyether (PE‐PU) and polyester (PES‐PU) diols is studies in light of recent molecular theories of rubber elasticity. The relationship between reduced stress (or modulus), extension ratio α, and network structure is discussed. In the range of low extensions, the deformation behavior of PESPU appears to be more affinelike than PE‐PU networks. When crosslinking agents with higher functionality are used, behavior closer to the affine limit is observed. Data in the low deformation range (α → 1) allow the estimation of network molecular weights predicted by the limiting phantom and affine networks. However, an exact determination of the true chain length cannot be obtained. The uncertainty in the molecular weight is due to the uncertainty in the theoretical structural parameter A'ϕ, which can assume values 1–2/ϕ ≤ A'ϕ ≤ 1. The range of possible network chain molecular weights can be narrowed when the real network, which always presents defects, is formed starting from building blocks of known molecular weight Ms, as in our case. In these real cases the molecular weight is between the value Ma Predicted by the affine model and the stoichiometric value Ms.

Analysis of stress‐induced crystallization in high‐cis‐1,4‐polybutadiene

AbstractStress‐induced crystallization of a crosslinked polybutadiene with a high 1,4‐cis content is investigated, at room temperature. The change in the fraction of crystallinity with deformation is evaluated by two different methods. The first is based on simultaneous measurement of birefringence and stress. The second is based on calorimetric analysis. The data on crystallinity obtained by these two methods are in good agreement in the range of low deformations, while, in the range of higher deformation (λ > 5), the degree of crystallinity obtained by calorimetry is higher than that obtained by the optical method. Qualitative information on the crystallization was also obtained by optical analysis of the hysteresis behavior. The hysteresis data show the presence of ordering phenomena at deformations at which there seems to be no crystallinity according to both quantitative methods.