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Applied impact test sample

Tensile and flexural properties were studied with an Instron 4204 testing machine. Tensile tests were performed on the drawn strands at a test speed of 3 mm/ min, while three-point-bending tests (ISO 178) at a speed of 5 mm/min were applied to the injection molded specimens. Charpy impact strength was measured of the unnotched samples with a Zwick 5102 pendulum-type testing machine using a span of 70 mm. The specimens (4 X 10 X 112 mm) used for three-point-bending tests were also used for the impact tests. It should be noted that neither the tensile tests for the strands nor the impact tests were standard tests. The samples were conditioned for 88 h at 23°C (50% r.h,) before testing. [Pg.625]

Dynamic Mechanical Testing - Film properties such as impact resistance and the cure response of thermosetting resins are conveniently investigated by dynamic measurements in which an oscillatory or torsional strain is applied to the sample with the stress and phase difference between the applied strain and measured stress being determined. In the present study, a Rheovibron Viscoelastometer was used which employed a sinusoidal strain at a... [Pg.375]

Somewhat more sophisticated instruments are frequently used for so-called instrumented impact tests. These instruments carry devices for measuring quantities such as the force applied to the sample and its displacement as a function of time and they allow the impact energy to be obtained more directly. Bending tests are, however, frequently carried out in a less sophisticated way using specimens without notches. The energy of fracture divided by the area of fracture is then called the impact strength. This quantity cannot be simply related to the quantities such as the critical strain-energy-release rate defined in fracture mechanics. [Pg.246]

Fig. 2. Survey of (electron and scanning force) microscopic methods for investigating micromechanical processes in polymers, a indicates the applied tension stress and the arrows indicate area and direction of investigation in the microscope (see text for full details), (a) fracture surfaces— tension test, impact test, broken pieces (b) surfaces of deformed (loaded) bulk samples (c) in situ deformation of thin samples. Fig. 2. Survey of (electron and scanning force) microscopic methods for investigating micromechanical processes in polymers, a indicates the applied tension stress and the arrows indicate area and direction of investigation in the microscope (see text for full details), (a) fracture surfaces— tension test, impact test, broken pieces (b) surfaces of deformed (loaded) bulk samples (c) in situ deformation of thin samples.
Dynamic Mechanical Analysis determines the elastic modulus (storage modulus), viscous modulus (loss modulus) and damping coefficient (Tan 5) as a function of temperature. The test specimens dimension was 3 mm X 13 mm x 20 mm and was the same for those used in the Izod impact test but without a notch. The test specimens were clamped between the movable and stationary fixtures, and then enclosed in the thermal chamber. The frequency, amplitude, and a temperature range of25-220°C were set-up for the material. The analyzer applied torsional oscillation to the test sample while slowly moving through the specified temperature range of 25-220°C. [Pg.51]

Generally speaking, when it comes to evaluating conventional materials, test samples for service life time estimation, quality, and safety analyses are collected. Data showing material characteristics are typically secured by means of optical and electron microscopes through destructive tests such as pull, compression, bending, torsion, creep, fatigue, impact, and corrosion. The same methods may be applied to a nanoscaled material. [Pg.410]

Protocols should require documentation of actual application practices and times. Samples of applied pesticides should be collected to document application rates to study sites. The test substance must be applied with typical equipment used for the crop, and the application must be made in accordance with the labeled use. Another variable that impacts such studies is the fact that most landowners have their own application equipment, which increases the variance in actual application rates among fields and may cause differential intra-field heterogeneity in application rates. [Pg.944]

Drop weight test A weight is dropped on a sample in a metal cup. The test measures the susceptibility of a chemical to decompose explosively when subjected to impact. This test should be applied to any materials known or suspected to contain unstable atomic groupings. [Pg.30]

The test method may specify either a notched sample or an unnotched sample. If a notched specimen is specified, the dimensions of the notch are also given. Figure 15.31 is an example of these dimensions for a metal sample. In the Charpy test the notched sample is struck from behind the notch. In the Izod test the notch is facing the hammer. The notch, called a stress raiser, concentrates the stresses applied by the impact load. It makes the material brittle and increases the elastic limit in the notch area. Without the notch, many materials will bend without fracture, and the capacity to absorb energy will not be accurately determined. [Pg.449]

Comparing the values of obtained at testing PP samples processed under various technological regimes and calculated with the aid of a mathematical model allows us to propose applying the criterion to the estimation of physical and chemical transformations occurring in a polymer at modifying the parameters of thermo-mechanical impact. [Pg.88]

Raman spectroscopy s sensitivity to the local molecular enviromnent means that it can be correlated to other material properties besides concentration, such as polymorph form, particle size, or polymer crystallinity. This is a powerful advantage, but it can complicate the development and interpretation of calibration models. For example, if a model is built to predict composition, it can appear to fail if the sample particle size distribution does not match what was used in the calibration set. Some models that appear to fail in the field may actually reflect a change in some aspect of the sample that was not sufficiently varied or represented in the calibration set. It is important to identify any differences between laboratory and plant conditions and perform a series of experiments to test the impact of those factors on the spectra and thus the field robustness of any models. This applies not only to physical parameters like flow rate, turbulence, particulates, temperature, crystal size and shape, and pressure, but also to the presence and concentration of minor constituents and expected contaminants. The significance of some of these parameters may be related to the volume of material probed, so factors that are significant in a microspectroscopy mode may not be when using a WAl probe or transmission mode. Regardless, the large calibration data sets required to address these variables can be burdensome. [Pg.199]

This is a very extensive topic involving many variables. It involves the evaluation of the inherent compatibility between a material and the environment under applied or residual stress. Factors such as material type, process history, product form, active cracking mechanisms, loading configuration and geometry and exposure environments can have an impact on the type of sample and test conditions for the evaluation of EAC. [Pg.111]


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