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Quantachrome

Manufactured by Anton Paar
Sourced in Austria, United States

The Quantachrome is an analytical instrument designed for the measurement of surface area, pore size distribution, and pore volume of solid materials. It utilizes gas adsorption techniques to provide accurate and reliable data on the physical properties of a wide range of materials, including catalysts, adsorbents, and pharmaceutical compounds. The Quantachrome is a versatile and essential tool for materials characterization in various industries.

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8 protocols using quantachrome

1

Characterization of Porous Activated Sawdust Carbons

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After the main structure had been, it was scrutinized employing a Fourier transform infrared (FT-IR) spectrometer (PerkinElmer, Waltham, MA, USA) in the range of 380–4000 cm−1. This was performed by incorporating the sample with the KBr disk (5% of the mixture). In order to characterize the composition, the prepared PASACs were coated with gold for analyses with scanning electron microscope (SEM, FEI Quanta FEG 250, Oregon, USA). Nitrogen adsorption, as assessed with the Brunauer–Emmett–Teller (BET) method, was used as a measure for the determination of the resulting surface area using Quantachrome (Nova, 2000e Quantachrome Instruments, USA). Additionally, the pore diameter was obtained by using the Barrett–Joyner–Halenda (BJH) method, and carbon (C), hydrogen (H), nitrogen (N), and oxygen were assessed in the samples. The elemental analyzer (Eurovector, EA3000-Single, Pavia, Italy) was used to determine the (O) content. A thermal gravimetric analyzer (TGA temperatures between 50 and 850 °C losses) was used to determine the thermal degradation ranges under continuous N2 flow at a heating rate of 15 °C/min.
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2

CO2 Adsorption Capacity Evaluation

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The CO2 adsorption experiments were carried out in dynamic conditions in a flow system. Prior to the start of the adsorption experiments, the adsorbent sample (0.40 g) was dried at 150 °C for 1 h. The experiments for CO2 adsorption were performed at 25 °C with 3 vol.% CO2/N2 at a flow rate of 30 mL/min. The samples were pressed and crushed in order to obtain materials with particle sizes of 0.2–0.8 mm. Additionally, the experiments for CO2 and water vapor adsorption (3 vol.% CO2 plus 1 vol.% water vapor) were performed at a 30 mL/min flow rate. The adsorption capacities of the materials were calculated based on the amounts of adsorbed CO2 and water vapor by using online GC analysis (gas chromatograph NEXIS GC-2030 ATF (Shimadzu, Kyoto, Japan) with a 25 m PLOT Q capillary column).
The CO2 adsorption measurements under static conditions were determined at 0 °C, 25 °C, and 50 °C with an AUTOSORB iQ-MP-AG (Anton Paar GmbH, Graz, Austria) surface area and pore size analyzer (from Quantachrome, Anton Paar GmbH, Graz, Austria). The Quantachrome software was used for the transformation of the primary adsorption data.
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3

Adsorbent Characterization and Analysis

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The characterization of the adsorbent was carried out before and after adsorption. Observing its surface morphology was investigated using a scanning electron microscope (SEM; Hitachi TM-1000, Tokyo, Japan) with a gold coating for 30 s. The volume and density of the pieces were determined by a gas pycnometer (Quantachrome, Ultrapyc 1200e Anton Paar, Graz, Austria). For the verification of chemical identity on the aerogel, a Fourier Transform Infrared Radiation (FTIR) spectroscopy was performed; using attenuated total reflection mode (ATR). These measures were taken at room temperature using an IR spectrophotometer (Alpha II Bruker, Billerica, MA, USA), analyzed in the range of 400–4000 cm−1.
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4

Evaluating Nanodiamond Pore Structure

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The pore structure of nanodiamonds was evaluated by nitrogen adsorption isotherms at 77 K. Samples of nanodiamonds after outgassing at 423 K for 2 h, 10 h, or 52 h were measured using a volumetric adsorption apparatus (Quantachrome-Autosorb IQ2, Anton Paar, Graz, Austria) to evaluate the porosity. Pore size distributions were determined by quenched solid density functional theory (QS–DFT) assuming a slit-shaped pore geometry model. Water adsorption isotherms were obtained at 298 K; the nanodiamonds were outgassed at 423 K for 2 h, 10 h, and 52 h, and the measurements were performed on a VSTAR instrument (Quantachrome, Anton Paar, Graz, Austria).
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5

Characterization of Porous Materials

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Brunauer–Emmet–Teller (BET) surface area, pore volume and radius were determined by N2 adsorption–desorption isotherms collected at 77 K using a Quantachrome instrument (Anton Paar, Graz, Austria). Prior to experiments, the samples were degassed at 393.15 K for 12 h. Pore structure parameters such as specific surface area, pore volume were calculated based on nonlocal density functional theory (NLDFT) method. The Brunauer–Emmett–Teller (BET) method was applied to calculate the specific surface area using N2 adsorption data in a relative pressure range from 0.05 to 0.25. The total pore volumes were estimated according to N2 uptake at a relative pressure (P/P0) of 0.99.
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6

Comprehensive Characterization of Sn1.5PW/Cu-BTC-1 Catalysts

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Fourier-transformed infrared spectroscopy (FTIR) spectra of the synthesized catalysts were obtained for powdered samples on KBr pellets using a PerkinElmer Spectrum 100 in the range of 400–4,000 cm−1. Wide-angle X-ray diffraction (XRD) patterns were recorded on a D8 ADVANCE (Germany) using CuKI (1.5406 Å) radiation to get insight into the composition of the catalysts. The morphology of the catalysts was obtained on a scanning electron microscope (SEM) at 2.0 kV (Hitachi S4800) and a transmission electron microscope (TEM) at 200 kV (FEI Tecnai G2 20). The BET surface area and pore size were determined based on nitrogen adsorption-desorption isotherms with a Quantachrome instrument (Quantachrome Instruments, Boynton Beach, USA). Thermogravimetric (TG) analysis was carried out in a NETZSCH/STA 409 PC Luxx simultaneous thermal analyzer; the samples were heated up from room temperature to 600°C at a heating rate of 5°C/min. The acidic properties of the Sn1.5PW/Cu-BTC-1 hybrid catalysts were characterized by temperature-programmed desorption (NH3-TPD) (Micromeritics AutoChem II 2920).
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7

Characterizing Acidic Alumina Surface

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Acidic γ-Al2O3 powder was provided from Sigma-Aldrich ® and dried at 110 °C in a desiccator for 24h to avoid the uptake of water vapor. The textural characteristics were evaluated by the adsorption of nitrogen (N2) at 77 K, and the BET (Brunauer-Emmett-Teller) model (Autosorb-1, Quantachrome instruments). Potentiometric titration was used to estimate the pHPZC of AA [21] .
The surface topographies of both fresh AA and AA adsorbed with fluoride were observed by means of scanning electron microscopy with energy dispersive spectroscopy SEM/EDS (S-520, Hitachi, Japan).
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8

Comprehensive Characterization of MOFs

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A JEOL JEM-2100 F TEM was applied for transmission electron microscopy (TEM) and High-angle annular dark-field scanning TEM (HAADF-STEM)-based elemental mapping at an acceleration voltage of 200 kV. The size distribution of the MOFs was carried out by using a Malvern Zetasizer Nano ZS instrument (Malvern Instruments, Malvern, UK). An UV-2600 UV–Vis spectrophotometer from Shimadzu was applied to note the UV–Vis absorption spectra. An absorption analyzer Quantachrome instruments (Florida, USA) was used to performed N2 adsorption/desorption isotherms (BET). X-ray diffraction (XRD) was detected by a Thermo Fisher ARL EQUINOX 3000 X-ray diffractometer. Fourier transform infrared spectroscopy (FTIR) was applied by a Thermo Fisher Nicolet 6700.
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