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Tga 50 analyzer

Manufactured by Shimadzu
Sourced in Japan

The Shimadzu TGA-50 analyzer is a thermogravimetric analysis (TGA) instrument designed to measure the weight changes of a sample as a function of temperature or time. It is capable of precisely measuring and recording the mass changes that occur in a material during heating, cooling, or isothermal conditions in a controlled atmosphere.

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12 protocols using tga 50 analyzer

1

Thermal Gravimetric Analysis of Aqueous Dispersions

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A typical
TGA sample was prepared by removing an aliquot amount (1 mL) of the
aqueous dispersion using a pipette to a clean scintillation vial and
drying it under high vacuum at room temperature. When the sample was
completely dry, the residue was dissolved in minimum amount of CHCl3 and the solution was carefully transferred into the TGA heating
pan, at which time the solution was completely evaporated in air before
the TGA experiment was started. The TGA experiment was performed on
a Shimadzu TGA-50 analyzer. The weight loss was analyzed by heating
the sample from room temperature to 500 °C at the rate of 5 °C/min.
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2

NMR and Thermogravimetric Analysis Protocol

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The 1H NMR spectra were measured using a JEOL AL-400
spectrometer operating
at a 1H resonance frequency of 400 MHz. The chemical shifts
were calibrated in ppm (δH) using tetramethylsilane (TMS) as the standard (0 ppm). Thermogravimetric
analysis (TGA) was conducted using a Shimadzu TGA-50 analyzer with
a heating rate of 5 °C/min under a N2 flow.
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3

Thermal Analysis of AXSA Films

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The TGA analyses were performed with Shimadzu TGA-50 analyzer (Kyoto, Japan). TG curves were obtained by heating weighed AXSA films from 30 to 600 °C at 20 °C. min−1 heating rate and 20 mL. min−1 nitrogen gas flow.
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4

Thermal Stability and Characterization of MIL-53(Al)

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The thermal stability of the adsorbent was assessed by thermogravimetric analysis (TGA) under N2 atmosphere using a Shimadzu TGA-50 Analyzer and was heated from 30–800 °C at a heating rate of 10 °C min−1. A Bruker D8 Advance X-ray diffractometer (XRD) was used to determine the crystallinity of the material. The functional group of the MIL-53(Al) was determined by scanning from 400 to 4000 cm−1 on a PerkinElmer FTIR spectrometer. Field emission scanning electron microscopy (FESEM) was used to determine the morphology using a Zeiss Supra 55 VP instrument, while the BET surface area and pore size were analysed using N2 adsorption–desorption with a Micrometric ASAP 2020.
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5

Thermal Characterization of Materials

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Thermal properties were determined by thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). TGA were performed on a Shimadzu TGA-50 analyzer from ambient temperature to 300 °C at 10 °C/min under nitrogen atmosphere. DSC thermograms were obtained in a Perkin-Elmer Pyris 1 calorimeter (PerkinElmer Inc., Waltham, MA, USA). Scans were carried out from 25 to 300 °C at a heating rate of 10 °C/min under a nitrogen atmosphere.
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6

Comprehensive Characterization of Synthesized MOFs

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The as-synthesized MOFs were characterized by field emission scanning electron microscopy (FESEM) (Zeiss Supra 55 VP instrument) for surface morphology. N2 adsorption–desorption (Micromeritics ASAP 2020) was used for surface area determination under liquid nitrogen. Powdered X-ray diffraction (XRD) (Bruker D8 Advance X-ray diffractometer) was used for crystallinity determination. The thermal stability of the adsorbents were analysed using thermogravimetric analysis (TGA) (Shimadzu TGA-50 Analyzer) under nitrogen gas atmosphere in a heating rate of 10 °C min−1 from 0–900 °C. Fourier transformed infrared spectroscopy (FTIR) (PerkinElmer FTIR spectrometer) was used for the analysis of functional groups using the attenuated total reflectance mode as sample introduction.
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7

Thermal Analysis of Dental Enamel

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Thermogravimetric analysis (TGA) was carried out using the TGA 50 analyzer (SHIMADZU CORPORATION, JAPAN). Each sample consisted of (4.00 ± 0.25) mg of powdered enamel placed in a platinum crucible. The TGA cycle was run between room temperature and 800 °C, at a rate of 10 °C/min with a 1-min hold at 30 °C. The measurements were carried out under oxygen (50 ml/min). The TGA curves are presented as a percentage of weight loss on the Y-axis (TGA%) and temperature (°C) in Fig. 2b.
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8

Biomass Characterization of WCSO

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The WCSO density was determined to find the mass of biomass that was processed at 500 µL, employing a portable density meter from Kem Kyoto electronics, model DA-130N, at 25.4 °C. The moisture and ash contents were analyzed according to ASTM D1762-84:2007 [41 ], employing a mass of 1.0000 g of WCSO. The moisture content was calculated from the mass loss after heating at 105 °C for 12 h. The ash content was determined by difference, after subjecting the samples to heating at 750 °C for 6 h. All of the analyses were performed in triplicate.
The thermal behavior of the WCSO was evaluated by thermogravimetric analysis (TG) and differential thermal gravimetric analysis (DTG), employing a Shimadzu TGA-50 analyzer. A 6.9 mg mass of sample was heated at a rate of 8 °C min−1 in the range 18–600 °C, under a nitrogen atmosphere at a flow rate of 40 mL min−1.
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9

Characterization of Gal-CMCS-Fe3O4-NPs

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Size, morphology, and electron diffraction of Gal-CMCS-Fe3O4-NPs were observed using a TEM (JEOL JEM-2010, Tokyo, Japan) operated at 200 kV. The size distribution and surface charge of Gal-CMCS-Fe3O4-NPs were measured as the zeta potential using a Nicomp 380 ZLS instrument (PSS, Santa Barbara, CA, USA). The surface chemistry of Gal-CMCS-Fe3O4-NPs was studied using a Fourier transform infrared spectrometer (AVATAR-370, Thermo, Madison, WI, USA) with KBr as a diluting agent and scanned against a blank KBr pellet background. A thermogravimetric analyzer (Shimadzu TGA-50 Analyzer, Tokyo, Japan) was used to perform thermal analyses. The saturation magnetization for Gal-CMCS-Fe3O4-NPs was done using Lake Shore 7407 vibrating sample magnetometer (Lake Shore Cryotronics, Westerville, OH, USA).
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10

Characterization of Thermochemical Liquid Crystal Droplets

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(1
where d is the interplane distance, θ is the position of the plane, n is a positive integer (1), and λ is the wavelength
The interatomic distance (a) was calculated using eq.2.
𝑎
Where. "d" is the interplane distance, and h, k, and l are the Miller indices.
The pH of TCLCDs was measured by a digital pH meter (PC 700, Eutech, Singapore) which was previously calibrated with pH 7, pH 4, and pH10 buffer solutions. The sample was diluted five times with millipore water, and the pH was measured. Thermogravimetric analysis (TGA) was performed on a Shimadzu TGA-50 analyzer by heating dried TCLCDs (4.268 mg) under the flow of N2 gas (100 ml/min) at the temperature rate of 10 °C/min up to 800 °C.
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