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Sdta851e

Manufactured by Mettler Toledo
Sourced in Switzerland

The SDTA851e is a simultaneous differential thermal analysis (SDTA) instrument designed for thermal analysis applications. It measures the temperature difference between a sample and a reference material as a function of time or temperature, providing information about the sample's thermal properties and behavior.

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6 protocols using sdta851e

1

Comprehensive Characterization of Reduced Graphene Oxide

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The electrochemical experiments were performed on a CHI660D electrochemical workstation (CH Instrumental Co., Shanghai, China). The morphology of RGO/CMC was observed by transmission electron microscopy (TEM, JEM-2010F UHR, JEOL Ltd., Tokyo, Japan). The spectral properties were characterized by ultraviolet-visible spectroscopy (UV-Vis, TU-1800PC, Puxi Tongyong Instrument, Beijing, China), Fourier-transform infrared spectroscopy (FT-IR, Nicolet-380, Thermo Electron Co., Waltham, MA, USA), Raman spectra instrument (Olympus FV1000, Olympus Co., Tokyo, Japan). The surface property of RGO/CMC colloidal aqueous solution was studied by Zeta potential analyzer (Zetasizer Nano, Malvern Instruments Ltd., Worcestershire, UK). The component percentage of sample were measured through thermal gravimetric analysis (TGA, SDTA851e, Mettler-Toledo Co., Zurich, Switzerland) with a heating rate of 10 °C·min−1 using pure nitrogen as a carrier gas. The crystal structures of GO and RGO/CMC were characterized by X-ray diffraction (XRD, X’Pert, Philips Co., Eindhoven, The Netherlands).
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2

Thermogravimetric Analysis of Biochar

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Moisture, fixed
carbon, volatile matter, and ash content in all biochars produced
were determined using a thermogravimetric analyzer, SDTA851e (Mettler
Toledo). The percentage of fixed carbon was determined by subtracting
the ash percentage from the volatile matter percentage after assigning
all weight loss up to 120 °C to loss of free and non-structural
water. Briefly, moisture content was measured as the weight loss after
the char was heated in a crucible from 25 to 120 °C and
held at this temperature for 3 min under a nitrogen gas environment
at a flow rate of 50 mL/min. Then, the char was heated from
120 to 950 °C under a nitrogen gas environment to determine
volatile content. It was then held at this temperature for 5 min
and cooled down to 450 °C. Ash was determined after heating
the char from 450 to 600 °C under oxygen gas flow (50 mL/min).
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3

Comprehensive Material Characterization Techniques

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The following characterization techniques were carried out for all prepared samples. The X-ray fluorescence (XRF) spectrometer NITON XL3t 900Analyzer with GOLDD Technology (Thermo Scientific, Waltham, MA, USA) was used for qualitative elemental characterization. Before performing the analysis, the NITON was allowed to warm up for a minimum of 15 min. Prior to measurements, the spectrometer was calibrated. The 4 μm thin film (3252 ULTRALANE®, Spex SamplePrep, Metuchen, NJ, USA) was stretched at one end of the double-opened ring cup (SC-4331, Premier Lab Supply, Port St. Lucie, FL, USA) and attached with an oversize ring. Samples were sprinkled into these cups. Cups with samples were placed over the detector and measured in “mining” mode.
Except for XRF characterization, all samples were well described in our previous work by field-emission scanning electron microscope (TESCAN MIRA 3, Oxford Instruments, Abingdon, UK) with energy-dispersive X-ray (EDX) detector, FTIR spectroscopy (VERTEX 70, Bruker Optics Inc., Billerica, MA, USA), CHNS elemental analysis (MACRO cube, Elementary Analysensysteme GmbH, Langenselbold, Germany), thermogravimetric analysis (SDTA851e, Mettler Toledo, Columbus, OH, USA), and N2; (−196 °C) physical adsorption (NOVA 1200e Surface Area and Pore Size Analyzer, Quantachrom Instruments, Boynton Beach, FL, USA) [23 (link)].
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4

Comprehensive Characterization of ACP and ZnO@ACP

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The ACP and ZnO@ACP were characterized to determine the surface properties. The morphology and elemental composition were analyzed by the field emission scanning electron microscopy (SEM; Jeol JSM-7800F model) coupled with energy-dispersive X-ray spectroscopy (EDS; Oxford X-max 80 mm2). The pore properties and surface area (SBET) were examined by the surface area analyzer (Micromeritics ASAP 2020 model) and results refined by MicroActive VI.01 software. The thermo-gravimetric analyzer (TGA; SDTA851e Mettler Toledo Model) with a 10 °C min−1 heating rate and 200 mL min−1 nitrogen flow rate analyzed the thermal stability. The pH drift method was used to determine the pH point of zero charged (pHpzc)11 . The surface functionality was examined by the Fourier transform infrared spectrometer (FTIR; Brucker Model). X-ray diffraction (XRD) was determined using an X-ray diffractometer (Brucker Model) with Cu radiation of 1.54 Å. Diffraction patterns were in the 2θ range of 10–80°, with a step size of 0.1° and 2 s counting time per step.
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5

Thermal Stability Analysis by TGA

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The thermal stability was tested by thermal gravimetric analysis (METTLER TOLEDO, SDTA851e, Switzerland) at a heating rate of 10 °C/min from 50 to 600 °C under a nitrogen atmosphere (25 ml/min).
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6

Comprehensive Characterization of Multi-Shelled ZIF-8 MOFs

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TEM images were obtained on JEOL JEM2010 operated at 200 kV. TGA was conducted on a METTLER TOLEDO’s SDTA851e simultaneous thermal analyzer, collecting the thermogravimetric change data from 25 °C to 800 °C in a continuous flow of nitrogen for ~5 mg samples. Powder XRD patterns were recorded using a Rigaku Corporation’s Ultima IV X-ray diffractometer. FTIR spectra were collected using the iS50 Fourier transform infrared spectrometer from Nicolet. Particle size distributions were obtained using NANO ZS360 NANO particle size. STEM and EDX mapping experiments were performed on a FEI Probe Cs-corrected Titan operating at 200 kV. Confocal microscopy images were recorded using a Leica TCS SP8 STED 3X confocal laser scanning microscope to determine the presence and spatial location of the fluorophore-tagged enzymes in the multi-shelled (hollow) ZIF-8 MOFs. Ultraviolet-visible absorption spectra were collected using Agilent Cary 60 spectrophotometer. The nitrogen gas adsorption–desorption was measured at 77 K on a Quantachrome Autosorb-iQ-MP volumetric gas adsorption analyzer. Gas chromatography (GC) was conducted on Shimadzu’s GC-2010 pro.
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