Cross tensile test

Normalised fiber mechanical properties are expressed in terms of unit linear density. For example, in describing the action of a load on a fiber in a tensile test, units of N/tex or gram force per denier (gpd) are generally used. If this is done, the term tenacity should be used in place of stress. The tme units of stress are force per unit cross-sectional area, and the term stress should be reserved for those instances where the proper units are used. 

Ra.m Tensile. A ram tensile test has been developed to evaluate the bond-2one tensile strength of explosion-bonded composites. The specimen is designed to subject the bonded interface to a pure tensile load. The cross-section area of the specimen is the area of the aimulus between the outer and inner diameters of the specimen. The specimen typically has a very short tensile gauge length and is constmcted so as to cause failure at the bonded interface. The ultimate tensile strength and relative ductihty of the explosion-bonded interface can be obtained by this technique. 

In addition to the above techniques, inverse gas chromatography, swelling experiments, tensile tests, mechanical analyses, and small-angle neutron scattering have been used to determine the cross-link density of cured networks (240—245). Si soHd-state nmr and chemical degradation methods have been used to characterize cured networks stmcturaHy (246). H- and H-nmr and spin echo experiments have been used to study the dynamics of cured sihcone networks (247—250). 

Sketch curves of the nominal stress against nominal strain obtained from tensile tests on (a) a typical ductile material, (b) a typical non-ductile material. The following data were obtained in a tensile test on a specimen with 50 mm gauge length and a cross-sectional area of 160 mm. ... 

Test rate and property The test rate or cross-head rate is the speed at which the movable cross-member of a testing machine moves in relation to the fixed cross-member. The speed of such tests is typically reported in cm/min. (in./min.). An increase in strain rate typically results in an increase yield point and ultimate strength. Figure 2-14 provides examples of the different test rates and temperatures on basic tensile stress-strain behaviors of plastics where (a) is at different testing rates per ASTM D 638 for a polycarbonate, (b) is the effects of tensile test-... 

Young s moduli of the polymers were determined in tensile tests [53] using samples of 4 mm by 10 mm cross-section and a gauge length of 50 mm. The results of the... 

Tensile testing samples were of miniature size (ca. 1.5x1.8 mm in cross-section and 5-5 cm in gauge length. Long practice in this Laboratory has proven that samples of this size give reproducible results and are eligible for comparison purposes. 

It is also possible to mn tensile tests at a constant rate of loading. If the cross-sectional area is continuously monitored and fed back into a control loop, constant-stress-rate tests can be made. In this case the initial slope... 

Several additional, non-microstructural, inputs are required for the fracture model (i) Particle critical stress intensity factor, KIc. Here, the value determined in a previous study (Klc = 0.285 MPa in )[3] was adopted for all four graphites studied. This value is significantly less than the bulk Klc of graphites (typically -0.8-1.2 MPa rn). However, as discussed in the previous section, when considering fracture occurring in volumes commensurate in size with the process zone a reduced value of Klc is appropriate (ii) the specimen volume, taken to be the stressed volume of the ASTM tensile test specimens specimen used to determine the tensile strength distributions and (iii) the specimen breadth, b, of a square section specimen. For cylindrical specimens, such as those used here, an equivalent breadth is calculated such that the specimen cross sectional area is identical, i.e.,... 

Apart from the short beam shear test, which measures the interlaminar shear properties, many different specimen geometry and loading configurations are available in the literature for the translaminar or in-plane strength measurements. These include the losipescu shear test, the 45°]5 tensile test, the [10°] off-axis tensile test, the rail-shear tests, the cross-beam sandwich test and the thin-walled tube torsion test. Since the state of shear stress in the test areas of the specimens is seldom pure or uniform in most of these techniques, the results obtained are likely to be inconsistent. In addition to the above shear tests, the transverse tension test is another simple popular method to assess the bond quality of bulk composites. Some of these methods are more widely used than others due to their simplicity in specimen preparation and data reduction methodology. 

The tensile test is typically destructive that is, the sample is extended until it plasticly deforms or breaks, though this need not be the case if only elastic modulus determinations are desired. As described in the previous section, ductile materials past their yield point undergo plastic deformation and, in doing so, exhibit a reduction in the cross-sectional area in a phenomenon known as necking. 

It can be concluded that it is very difficult to predict the result from a polymer macrostructure, but it is relatively easy to measure the secondary species generated on irradiation by using known analytical techniques, such as measuring swelling, tensile tests, analysis using nuclear magnetic resonance (NMR), etc. The yield is then expressed by the G value, which represents the number of cross-links, scissions, double bonds, etc., produced for every 100 eV (1.6 X 10 J) dissipated in the material. For example, G (cross-links), abbreviated G(X), = 3.5 means that 3.5 cross-links are formed in the polymer per 100 eV under certain irradiation conditions. Similarly, the number of scissions formed is denoted by G(S). In order to determine the number of crosslinks or G(X), the number of scissions or G(S), etc., it is necessary to know the dose or dose rate and the time of exposure for these irradiation conditions. From the product yields it is possible to estimate what ratio of monomer units in a polymer is affected by irradiation. ... 

Swelling tests and determination of tensile properties. The procedure for estimating cross-link density from equilibrium swelling data is described in detail in a previous paper (6). The tensile properties of the PU films were carried out at 23°C and 60% relative humidity. The crosshead speed and distance were 10 mm/min and 30 mm, respectively. A more detailed description of the tensile tests is given elsewhere (6). 

A series of six stress-strain cycles with a crosshead rate of 600 mm/min was applied to specimens having a parallel length of 25 mm and a cross-section of 1 x 4 mm2 on a tensile testing machine. The samples were continuously stretched in six hysteresis cycles up to 60% of their elongation at break values, as shown in Fig. 47. This procedure is an established one and widely practiced for elastomeric composites reinforced with fillers such as carbon black and silica, which tend to build a strong filler-filler network [83]. 

The resistance to fluid flow is a measure of the physical structure of the foam. In order to control the flow through a foam, ceU size, degree of reticulation, density, and other physical factors must be controlled. The control of these physical factors, however, is achieved through the chemistry and the process by which the foam is made. The strength of the bulk polymer is measured by the tensile test described above, but it is clear that the tensile strengths of the individual bars and struts that form the boundaries of an individual cell determine, in part, the qualities of the cells that develop. A highly branched or cross-linked polymer molecule will possess certain tensile and elongation properties that define the cells. The process is also a critical part of the fluid flow formula, mostly due to kinetic factors. As discussed above, the addition of a polyol and/or water to a prepolymer initiates reactions that produce CO2 and cause a mass to polymerize. The juxtaposition of these two reactions defines the quality of the foam produced. Temperature is the primary factor that controls these reactions. Another factor is the emulsification of the prepolymer or isocyanate phase with the polyol or water. 

In the interests of standardisation it is desirable to limit as far as possible the variety of test piece sizes allowed. Success in this direction has not always been possible, as illustrated by the tensile test pieces detailed in ASTM D412. However, there would be no need to limit dimensions at all if it were not a fact that the size of test pieces can affect the magnitude of the result obtained, or at least the variability. In the case of tensile tests, the difference in level between results from rings and dumb-bells has already been mentioned. The variability of the two types of test pieces has been found to be similar. The measured tensile strength has a tendency to decrease with increasing cross-sectional area of the test piece and it is desirable to make comparisons only between groups of test pieces of nominally the same type and thickness. The difference between the results from type 1 and 2 dumb-bells is not normally significant but Bartenev and... 

The measurement of dimensions is covered in chapter 7. It is, however, necessary to stress the importance of accurate measurement of the small cross-sectional area of tensile test pieces. 

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