General properties tensile

Post-Curing. Post-curing at elevated temperatures develops maximum physical properties (tensile strength and compression-set resistance) in fluorocarbon elastomers. General post-cure conditions are 16 to 24 h at 200 to 260°C. 

The tensile properties (tensile strength, Young s modulus, and elongation) of unoriented, noncrystalline films were investigated for those polymers that formed clear films by solvent casting. The results collected in Table I allowed several general conclusions. 

Influence of the ZnCFO contents (3,0 5,0 7,0 phr) on crosslink kinetics of the modelling unfilled rubber mixes from NBR-26 of sulfur, thiuram and peroxide vulcanization of recipe, phr NBR-26 - 100,0 sulfur - 1,5 2-mercaptobenzthiazole - 0,8 stearic acid - 1,5 tetramethylthiuramdisulfide - 3,0 peroximon F-40 - 3,0, is possible to estimate on the data of fig. 7. As it is shown, the increase of ZnCFO concentration results in increase of the maximum torque and, accordingly, crosslink degree of elastomeric compositions, decrease of optimum cure time, that, in turn, causes increase of cure rate, confirmed by counted constants of speed in the main period (k2). The analysis of vulcanizates physical-mechanical properties testifies, that with the increase of ZnCFO contents increase the tensile strength, hardness, resilience elongation at break and residual deformation at compression on 20 %. That is, ZnCFO is effective component of given vulcanization systems, as at equal-mass replacement of known zinc oxide (5,0 phr) the cure rate, the concentration of crosslink bonds are increased and general properties complex of rubber mixes and their vulcanizates is improved. 

The increment in mechanical properties (tensile strength, 300% modulus, and Young s modulus) as a function of SAF is plotted in Fig. 39. In general, the higher level of SAF, which in turn indicates better exfoliation, results in high level of property enhancement. However, the level of increment with the increase in SAF is different in all three cases and follows a typical exponential growth pattern. The apparent nonlinear curve fitting of the experimental values presented in Fig. 39 is a measure of the dependence of mechanical properties on the proposed SAF function. 

For this comparison, a melt-spinning process was chosen. Each special thermoplastic process influences the structure and thus the properties of the obtained polymer samples differently. This is particularly pronounced for fibers, since especially melt spinning is a process which makes extremely high demands on the deformation ability of the polymer melts at high deformation speeds. Particularly the tensile stress within the fiber formation zone is a very important factor to reach a high orientation of the macromolecules along the fiber axis and a stress-induced crystallization. This crystallization should be discussed in relation to PLA and PHB multifilaments, and at the same time the general property spectrum of these polymers should be represented. 

Figure 9.5 illustrates the general trends for tread-grade carbon black loading and the effect on compound physical properties. As carbon black level increases, there are increases in compound heat buildup and hardness and, in tires, an increase in rolling resistance and wet skid properties. Tensile strength, compound processability, and abrasion resistance, however, go through an optimum after which these properties deteriorate. 

Strain-induced crystallization is the property that makes NR a very strong matrix because of its. It has been observed that generally the tensile strength shows initial drop down to a certain amount of fibre and then increases. The fibre reinforces the matrix above critical volume which is the minimum volume... 

The general physical and mechanical properties of fluoroelastomers are similar to those of other synthetic rubbers. Fluoroelastomer compounds have good tensile strengths, ranging from 188 to 2900 psi. In general, the tensile strength of any elastomer tends to decrease at elevated temperatures however, loss in tensile strength is much less with the fluoroelastomers. 

Crosslinking causes changes in the physical properties of NR, as summarized in Table 12.3. Generally, the tensile strength and modulus increase on cross-linking, while the elongation at break decreases. Heat and solvent resistance are improved by crosslinking. 

Since molded graphite does not deform plastically, at least at low temperatures, measurement of its tensile strength is difficult and unreliable. Instead, it is preferable to measure flexural (transverse) strength, which is a more reproducible property. Tensile strength is generally 50 to 60% of the flexural strength and compressive strength is approximately twice as much. 

Figures 10.9 to 10.11 illustrate how stretching curves and critical strains vary with temperature, again with results for PEVA12, and with the crystallinity here polyethylenes with different crystallinities are compared. Curves demonstrate a further general property of semicr3 talline pol5oners. While the stresses vary in systematic manner, there is no effect on the critical strains for softening (en 0.1) and hardening (en 0.6) and virtually no change in the elastic-plastic composition of the strains. Hence, tensile deformation of semicrystalline polymers is strain-controlled and changes the mechanism at two critical strains that are temperature and crystallinity invariant.

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