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Tga400

Manufactured by PerkinElmer
Sourced in United States

The TGA400 is a thermogravimetric analyzer (TGA) that measures the change in weight of a material as a function of temperature or time in a controlled atmosphere. It provides quantitative analysis of the composition of materials and their thermal stability.

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17 protocols using tga400

1

Iron Citrate Complex Characterization

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All reagents, solvents and standards used to produce the iron citrate neutral complex were obtained from different suppliers and all were of high purity: iron filings (>99%), citric acid monohydrate (>99.5%), iron sulphate heptahydrate, 1,10-ortho-phenanthroline and potassium thiocyanate pure for analysis were purchased from Sigma-Aldrich (Buchs, Switzerland). Ultrapure water was produced by a milli-Q generator (Millipore, Bedford, MA, USA). Potassium sulfocyanide pure for analysis from Carlo Erba (Milan, Italy). Analytical balance series B 204 S (Mettler-Toledo, Germany), freeze dryer mod. Heto Lyolab 3000 (Analytical De Mori, Milan, Italy). UV-Vis spectrophotometer, mod UV-1601 (Shimadzu, Tokyo, Japan), quartz cuvettes with optical path of 1.00 cm. Automatic powder diffractometer Panalytical Empyrean Powder (Santa Barbara, CA, USA) and automatic analyser for the determination of total organic carbon Skalar Analytical B.V (Breda, The Netherlands) were used. Thermogravimetric analyser TGA400 Perkin Elmer (Norwalk, CT, USA).
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2

Thermogravimetric Analysis of Samples

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The thermogravimetric analysis (TGA) was performed with a thermogravimetric analyzer (TGA 400 PerkinElmer). Samples were about 5 mg and the heating cycle was from 50 to 800 °C at a heating rate of 10 °C min−1 under air flow.
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3

Thermal Stability Analysis of OFE Extracts

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Thermogravimetric analysis (TGA) is a widely used technique to evaluate the thermal stability of compounds in which the loss of mass as a function of temperature is measured. OFE extracts were examined through a PerkinElmer TGA-400 instrument (PerkinElmer Inc. Waltham, USA). Briefly, 5–10 mg samples were heated in a nitrogen atmosphere in the range of 30–800 °C with a constant flow rate (20 °C/min) and a gas flow set at 20 mL/min. The TGA Pyris series software was exploited to record thermograms (TG) and calculate their respective derivative curves (DTG) for further data mining.
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4

Thermal Analysis of Modified Particles

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The weight loss of
the (modified) particles as a function of temperature was measured
with a TGA400 (PerkinElmer, Inc., Waltham, MA). A sample weighing
∼5–10 mg was loaded into a platinum pan, and the temperature
was set to 50 °C to stabilize. Subsequently, the sample was heated
to 900 °C at a heating rate of 20 °C min–1. The applied air flow was 20 mL min–1.
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5

Thermal Stability Analysis of Essential Oils

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Thermogravimetric (TGA) is a widely used technique to evaluate the thermal stability of materials in which the loss of mass as a function of temperature is measured. EOs were examined through a PerkinElmer TGA-400 instrument (PerkinElmer Inc., Waltham, MA, USA). Briefly, 5–10 mg samples were heated in an air-saturated atmosphere in the range of 30–800 °C, with a constant flow rate (20 °C/min) and a gas flow set at 20 mL/min. The TGA Pyris series software (PerkinElmer Inc., Waltham, MA, USA) was exploited to record Thermograms (TG) and calculate their Respective Derivative Curves (DTG) for further data mining.
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6

Thermal Analysis of Material Samples

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Differential Scanning Calorimetry (DSC) analysis was performed using a Discovery DSC1-0145 (TA-Instrument New Castle, DE; USA). All the analyzed samples were heated from 15 to 70 °C (1st heating), then cooled down from 70 to -80 °C and finally heated up to 70 °C (2nd heating). The thermal scans were recorded at a scan speed of 5 °C/min under nitrogen flow in aluminum sealed pans. Thermograms were analyzed using the TA Universal Analysis software.
Thermo-Gravimetric Analysis (TGA) was performed on a PerkinElmer TGA-400 instrument (PerkinElmer Inc.), heating 5–10mg of samples in air-saturated atmosphere, and setting the gas flow to 20 mL/min. The flow rate was set to 20 °C/min, heating from 30 to 800 °C. For each sample, thermograms (TG) with respective derivative (DTG) curves were recorded and analyzed with the TGA Pyris software.
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7

Thermal Characterization of Nanosystem

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Thermal decomposition of the nanosystem was observed via Thermogravimetric analysis (TGA), heated from 20 °C to 900 °C under nitrogen atmosphere at a flow rate of 20 mL/min. The thermal decomposition analyses of the samples were determined using a TGA 400 thermogravimetric analyser (PerkinElmer Inc., Waltham, MA, USA). Thermal properties of the nanosystem and its components were explored using differential scanning calorimetry (DSC) (Mettler Toledo, Schwerzernback, Switzerland). Freeze-dried samples were weighed (3–10 mg) into aluminium pans and analyzed under nitrogen atmosphere (Afrox, Germiston, Gauteng, South Africa) with 200 mL/min flow rate and the samples were then heated from 25 °C to 300 °C at the rate of 10 °C/min.
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8

Physicochemical Characterization of Pineapple Leaves

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A Jenway pH meter was used for the preparation of different pH dye solution. An ST8 Benchtop Centrifuge (Thermo Scientific, Waltham, MA, USA) was used for separating the components of each sample mixture. The absorbance was measured using an UV–Vis spectrophotometer (Agilent DAD, Agilent, Santa Clara, CA, USA). The surface morphology of the prepared pineapple leaves was identified using a scanning electron microscope (SEM– Quanta 200, Thermo Scientific, Waltham, MA, USA) and energy–dispersive X–ray spectroscopy (EDX, Thermo Scientific, Waltham, MA, USA). Fourier transform infrared radiation (FT-IR, Bruker Alpha, MA, USA) was used to determine the functional groups on the surface of pineapple leaf. The Raman spectrum was recorded in the range from 50–3500 cm−1 using a Raman microscope (DXR Raman Microscope, Thermo Scientific, Waltham, MA, USA), with a laser beam at 532 nm as excitation source. Furthermore, a thermal gravimetric analyzer (TGA400, PerkinElmer, Waltham, MA, USA was utilized to inspect the thermal stability of the pineapple leaf. Finally, Minitab®19 software (Minitab Inc., Chicago, IL, USA) was used to construct the face–centered central composite design (FCCCD).
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9

Synthesis and Characterization of Gold-Coated Core-Shell Magnetic Nanoparticles

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Minitab®18 software (Minitab Inc., State College, PA, USA) was operated for building the implemented full factorial design (2k-FFD) [47 ]. ZEN® 2.3 “Blue edition” lite Digital Imaging Software (Carl Zeiss, Promenade 10, 07745 Jena, Germany) was used to measure the diameter of the NPs in the images obtained by the scanning electron microscope (SEM). An OriginPro software (OriginLab, Northampton, MA) was utilized to execute histograms for PSD.
A Field Emission Scanning Electron Microscopy (FEI SEM, Quanta650FEG FESEM, Czech Republic: Imaging and Characterization Core Labs facility at QEERI, Hamad Bin Khalifa University, HBKU, Qatar) with a resolution power of 1.2 nm was used to describe the produced gold coated core–shell mNPs (A fine powder was dispersed onto adhesive carbon tape and sputter coated with Au.) in terms of PS, PSD, and morphology. FT-IR (Agilent, Cary 670, Santa Clara, CA, USA) with an ATR unit (PIKE, gladiATR) was used to identify the functional groups of the magnetic particles. Thermal gravimetric analyzer (TGA, PerkinElmer—TGA 400) was used to measure the decomposition of the modified NPs with respect to temperature. Analytical Balance Kern (ABT 120-5DNM) was used to determine the yield as well as the attraction weight by using neodymium magnet (96.475 g).
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10

Thermal Behavior of Hybrid Composites

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The thermal behavior of the hybrid composites was assessed by a PerkinElmer TGA-400 instrument (Perkin Elmer, Milan, Italy), heating 5–10 mg of the samples between 30 and 600 °C. The analyses were performed in nitrogen, with a gas flow set at 20 °C/min. Data were recorded by means of the TGA Pyris software (version 13.3.1.0014).
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