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Dma q800 analyzer

Manufactured by TA Instruments
Sourced in United States

The DMA Q800 is a dynamic mechanical analyzer (DMA) that measures the mechanical properties of a wide range of materials, including polymers, composites, and biological samples. The DMA Q800 applies a small, controlled force to a sample and measures the sample's response, providing information about the material's stiffness, damping, and other viscoelastic properties.

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12 protocols using dma q800 analyzer

1

Characterization of Polymer Nanocomposites

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Fourier transform infrared (FTIR) analysis was performed on a PerkinElmer 1000 FTIR spectrometer (PerkinElmer, Waltham, MA USA) at room temperature with a resolution of 1 cm−1 in a transmission mode. The number of the scan was 10. The mechanical test of the nanocomposites was carried out in a universal testing machine (Hounsfield H10KS, Redhill, UK) with a cross head speed of 100 mm/min. Thin films (60 mm × 10 mm × 0.2 mm) were used for mechanical tests. A dynamic mechanical analysis (DMA) of the WPUs and the nanocomposites was carried out in a Q800 DMA analyzer (TA Instruments, New Castle, DE, USA) at a heating rate of 2 °C from −50 to 150 °C. The test mode was a single cantilever with a frequency of 1 Hz and amplitude of 5%.
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2

Dynamic Mechanical Analysis of Polymer Samples

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HDT was measured employing a Q800 DMA analyzer (TA Instruments, Pittsburgh, PA, USA). The testing method was three-point bending, and the heating rate was 2 °C/min, from room temperature to 70 °C. Each sample had a length of 50 mm (LDMA), a width of 5.5 mm (WDMA), and a thickness of 0.45 mm (TDMA). By following ASTM D648, a 0.455 MPa stress (σ) was applied, and the Dynamic Mechanical Analysis (DMA) analyzer was set to show the plot “sample strain” (or sample deflection) versus “temperature”. The strain (or deflection) at which the deflection temperature was taken could be calculated through the following procedure. Given the applied stress (0.455 MPa) and the sample dimensions, Equation (2) allowed the calculation of the applied force (F): F=23[σ(TDMA2×WDMALDMA)].
In our case, F = 6.8 kN. Next, the strain (ε) in the American Society for Testing and Materials (ASTM) sample, at a deflection (dASTM) of 0.25 mm, could be calculated: ε=6(dASTM×TASTMLASTM2)=0.00121=0.121%.
TASTM = 13 mm and LASTM = 127 mm are the sample thickness and length, respectively, according to ASTM D648. Lastly, the sample deflection (dDMA) at which the deflection temperature was taken could be calculated: dDMA=ε[LDMA2(6×TDMA)].
In our case, dDMA = 1.8 mm. Four specimens were considered for each test.
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3

Dynamic Mechanical Characterization of Cured Samples

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The dynamic mechanical behaviors of tested samples, including storage moduli and tan δ values, were measured using a TA Instruments DMA Q800 analyzer via a three-point bending model with an oscillation frequency of 1 Hz. The testing temperature ranged from 0 to 160 °C at a heating rate of 5 °C min−1. Cured samples with dimensions of 20 mm (length) × 10 mm (width) × 4 mm (thickness) were used for testing.
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4

Thermomechanical Analysis of Printed TPU

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DMA Q800 analyzer (TA Instruments, New Castle, DE, USA) was used to perform dynamical mechanical tests. The measurements were carried out in the single cantilever bending mode with 1 Hz frequency of an oscillatory deformation on printed TPU samples (40 × 10 × 2 mm3 dimension), at the temperature range of −100 °C to 150 °C (heating rate 4 °C min−1). The storage modulus (G’), loss modulus (G’’), and damping factor (tangent δ) were determined as a function of temperature.
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5

Dynamic Mechanical Analysis of Composites

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DMA of composites was performed in tensile mode using a DMA Q800 Analyzer TA Instruments (New Castle, DE, USA). Calibration was performed as per the manufacturer’s recommendations included in Advantage Software, version 5.5.24 (TA Instruments, New Castle, DE, USA). The experiments were carried out on rectangular samples of dimensions close to 3 mm thick, 10 mm wide, and 60 mm long. Experimental conditions employed were a frequency of 1 Hz and amplitude of 10 μm with the scanning air temperature range from −100 °C to 127 °C and a temperature ramp of 3 °C/min. The variations of storage modulus (E′), loss modulus (E″), and tangent delta (tan δ) versus temperature were determined.
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6

Three-Point Bending DMA Analysis

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DMA tests use a DMA Q800 analyzer (TA Instrument, USA) to perform a three-point bending test at a heating rate of 5°C/min and a load frequency of 1 Hz. A rectangular sample with a size of 60 × 10 × 2 mm3 was used for measurements in the range of 25–200°C.
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7

Dynamic Mechanical Analysis of Bio-TPU

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Dynamic mechanical analysis of bio-TPU obtained in [NCO]/[OH] molar ratio equaled 1.0 was performed according to ASTM D4065:2012 using a DMA Q800 Analyzer (TA Instruments, New Castle, DE, USA) under nitrogen atmosphere. The measurements were made at a temperature range from −100 to +120 °C, at an operating frequency of 10 Hz. The heating rate was 4 °C/min. The dimension of rectangular samples was ca. 18 × 10 mm, and a thickness of 3 mm. The values of storage modulus (E′), loss modulus (E″), and glass transition temperature of soft segments, TgSS (based on the dependence of tanδ upon temperature) were also determined.
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8

Dynamic Mechanical Analysis of Bio-TPU

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Dynamic mechanical analysis of bio-TPU was performed using a DMA Q800 Analyzer (TA Instruments, New Castle, DE, USA). Measurements were carried out according to ASTM D4065:2012 [22 ]. Measurements were taken in the three-point bending mode at an operating frequency of 10 Hz. The measurements were made at temperatures ranging from −100 to 150 °C with a heating rate of 3 °C/min.
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9

Dynamic Thermal-Mechanical Characterization

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Dynamic Thermal-Mechanical properties were performed using the DMA (DMA Q800 analyzer, TA instruments, USA) in tension mode. The samples used were long strips with dimensions of 1 × 4 mm. The following testing conditions were applied: an amplitude of 20 um, a scanning starting temperature of −80 °C, a termination temperature of 40 °C, and a heating rate of 3 °C/min.
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10

Comprehensive Characterization of Polymer Composites

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Fourier transform infrared (FTIR) spectra of the films were recorded using an attenuated total refraction (ATR) accessory with a ZnSe plate. Measurements used an FTIR spectrometer (Bruker, Tensor 37, Karlsruhe, Germany) with spectral resolution of 1 cm−1 and 32 scans in the wavelength range of 4000–400 cm−1. Thermogravimetric analysis (TGA) was carried out with a TA Instrument Q600 analyzer (New Castle, DE, USA) under a nitrogen atmosphere in a temperature range of 30–600 °C with a heating rate of 10 °C/min and using platinum pans. Dynamic mechanical analysis (DMA) was performed on a TA Instruments DMA Q800 analyzer (New Castle, DE, USA) in the multifrequency mode using a dual cantilever clamp at 1 Hz in frequency. The samples were tested from –50 to 100 °C with a heating rate of 5 °C/min. The morphology of the composites was observed by scanning electron microscopy (SEM) using a Hitachi TM-1000 microscope (Tokyo, Japan) at an accelerating voltage of 15 kV. Samples were mounted on metal stubs and were vacuum coated with gold at 7 × 10−2 mbar using argon in an EMS 550 sputter coater. The tensile tests were carried out on a mechanical Zwick/Roell model Z005 tester (Ulm, Germany), with a load cell of 5000 N and at a speed of 50 mm/min. Dog-bone shaped specimens were made according to ASTM D638 [37 ], and five specimens were performed.
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