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Tensile machine

Manufactured by Instron
Sourced in United States

The Tensile machine is a testing device used to measure the mechanical properties of materials under tension. It applies a controlled pulling force to a specimen until it breaks, providing data on the material's strength, stiffness, and ductility. The machine can accommodate a variety of sample sizes and materials, making it a versatile tool for material testing and quality control applications.

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Lab products found in correlation

9 protocols using tensile machine

1

Mechanical Characterization of Grafts

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Burst pressure, ultimate tensile strength (UTS) and Young’s modulus of grafts (N = 4 in each group) were measured with an electronic manometer (Extech instruments HD750) or an Instron tensile machine (Norwood, MA, USA) as described previously10 (link).
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2

Hydrogen Charging and Tensile Testing

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Hydrogen charging was carried out by an electrochemical method at 50 mA cm−2 current density in a 0.5 M H2SO4 solution with 5 g L−1 thiourea (CH4N2S) at the temperature of 298 K. The counter electrode was a piece of platinum plate. The samples were first pre-charged for 24 h at 50 mA cm−2. After that they were continuously in situ charged during the entire duration of the tensile tests. The uniaxial tensile tests were conducted in an Instron tensile machine with an initial strain rate of 1 × 10−4 s−1 at a temperature of 300 K. The tensile specimens with gage dimensions of 3 mm × 1 mm × 10 mm were prepared along the rolling direction by spark cut. The gage part of the tensile specimens was charged with hydrogen. The hydrogen desorption was investigated via a custom-designed UHV-based Thermal Desorption Analysis instrument in conjunction with a Mass Spectrometer detector. The heating temperature range was selected from 25 °C up to 800 °C with a constant heating rate of 26 °C min−1. The total hydrogen concentration stored in the MEA samples was determined by conducting cumulative desorbed hydrogen probing during a heating experiment using a gradual heating rate up to 800 °C.
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3

Hydrogen Charging and Tensile Testing

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Hydrogen was introduced into the specimens by electrochemical charging with various current densities at ambient temperature (25 °C) in 0.1 M NaOH solution plus 0.05 g·L−1 CH4N2S at pH = 13. A platinum wire was used as the counter electrode. The samples were pre-charged for 12 h at 15 mA·cm−2, 72 h at 25 mA·cm−2, and 240 h at 100 mA·cm−2, respectively. Then the samples were continuously in-situ charged during the entire tensile testing to avoid the release of hydrogen. The tensile tests were conducted in an Instron tensile machine at the tensile rate of 1 × 10−4 S−1. Uniaxial tensile tests were conducted using specimens with thickness of 1.5 mm and gauge length of 10 mm. Three samples for each condition were tested to confirm reproducibility. The hydrogen desorption rates were measured by using a custom-designed UHV-based Thermal Desorption Analysis instrument in conjunction with a Mass Spectrometer detector set up (TDA-MS) from 25 °C to 800 °C, and the corresponding heating rate was 26 °C min−1. The diffusible hydrogen concentration was determined by measuring cumulative desorbed hydrogen from 25 °C to 600 °C.
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4

Tensile Testing of tetraSH-DVO2 and polySH-DVO2

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The tensile testing was carried out using Instron tensile machine with tensile mode (1 mm/min to break). When the cyclic tensile testing was conducted, the samples were stretched to 30% strain compared to original length and then gradually pushed back to original length with the rate of 1 mm/min. For both tetraSH-DVO2 and polySH-DVO2 with and without thermal post curing, 6 samples were tested in tensile testing.
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5

Tensile Behavior of Polymer Materials

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An INSTRON tensile machine was used to
evaluate the mechanical parameters of the polymers in a dog-bone shape
(dimensions in Figure S5). The rate of
extension was set to 5 mm min–1. For each type of
sample, at least three repetitions were carried out. The test results
were then analyzed to create a stress–strain curve from which
Young’s modulus, maximum tensile strength, and elongation at
break values were taken. For the wet (swollen) condition, the test
was carried out right after taking the specimen out of the water,
while the dry samples were dried and placed in a desiccator for 72
h before testing.
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6

Mechanical Properties of Molded Specimens

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Example 5

Tensile and flexural properties were determined from the compression molded dog-bone and rectangular specimens, respectively. The samples were molded at 190° C. and were subsequently conditioned at 100° C. in temperature controlled compression molding platens. Tensile testing was performed according to ASTM D 638 on an Instron tensile machine equipped with a 5 kN load cell and a cross head speed of 5 mm min−1. Flexural tests were performed according to ISO 178 with a cross head speed of 2 mm min−1. All the mechanical tests were performed 48 h after molding and the reported values were obtained by averaging over eight specimens for each composition.

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7

Tensile Characterization of Silanized Composites

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In order to assess the benefits of the proposed silanization protocol, composite specimens were fabricated and the tensile properties were characterized. Tensile test specimens were manufactured by directly pouring the reactive mixture containing the treated particles into a mold in accordance with the ASTM D638 type 1 tensile geometry and cured at 180 °C. The tensile tests were performed using an Instron tensile machine equipped with a 50 kN load cell with a cross-head speed of 5 mm/min. The standard method recommends a thickness below 7 mm. In our case, an average thickness of 3.2 ± 0.5 mm was measured for all specimens.
All specimens were dried for at least 4 h at 70 °C before trials. A set of four composite samples of each surface chemistry was tested at 23 °C.
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8

Adhesive Strength Evaluation of Lining Systems

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The effectiveness of the adhesives was tested by separating the two joined surfaces and evaluating the force exerted, thus determining the adhesive strength of different lining systems. Adhesion analysis was performed by means of the peel and lap shear tests, which follow normative ASTM D1002 [27 ] and ASTM F88 [28 ], respectively. The tests were carried out using an Instron tensile machine, equipped with a 10 kN load cell. In both cases, prior to each test, the specimens were kept under controlled relative humidity equal to 75% at room temperature for 2 weeks. The preparation of the test specimens was carried out according to the procedure prescribed by each standard norm. The peel test speed was set equal to 256 mm/s, while a value of 1.3 mm/s was considered for the lap shear tests. For each sample type, 5 repetitions were performed.
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9

Tensile Mechanical Testing of Polymer Scaffolds

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Tensile mechanical testing was conducted using 10 mm× 20 mm sheets, per ASTM standards on an Instron Tensile machine using a 50-N load cell.41 (link) Scaffolds were incubated in PBS overnight prior to testing. A total of six measurements were averaged to obtain the tensile parameters for each polymer composition.
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