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Mini 2 analyzer

Manufactured by Microtrac

The Mini II analyzer is a compact and versatile particle size analyzer that measures the size distribution of particles suspended in liquid or dry powder samples. It utilizes the principles of laser diffraction to determine particle size information. The instrument provides accurate and reliable particle size data without interpretation or extrapolation.

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5 protocols using mini 2 analyzer

1

CO2 Adsorption and Hydration in Mg-CUK-1

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Adsorption Isotherms for CO2. Ultra-pure grade (99.9995%) CO2 gas was purchased from PRAXAIR. CO2 adsorption isotherms at 196 K and up to 1 bar were carried out on a Belsorp mini II analyzer under high vacuum.
Water-loading within Mg-CUK-1. H2O vapor loadings were performed by a dynamic method, using air gas as the carrier gas, and by using a DVS Advantage 1 instrument from Surface Measurement Systems (mass sensitivity: 0.1 mg, relative humidity (RH), accuracy: 0.5% RH, vapor pressure accuracy: 0.7% P/P0). Mg-CUK-1 samples were activated at 100 °C for 1 h under flowing dry N2. The water contents within Mg-CUK-1 analyzed were 25% RH, 22% RH, 20% RH and 18% RH.
Powder X-ray diffraction patterns were collected on a Rigaku Diffractometer, Ultima IV, with a Cu-Kα1 radiation (λ = 1.5406 Å) using a nickel filter. These were obtained from 5° to 50° in 2θ, with 0.02° steps at a 0.08° min−1 scan rate. Profile refinements were performed based on the previously reported Mg-CUK-1-hydrated structure data using the FullProf program (structure NUDLIJ from CCDC database) [14 (link),15 ].
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2

Hydrochar Characterization: Adsorption, Morphology, and Surface Properties

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The N2 adsorption/desorption behavior of hydrochars were determined at 77 K using Belsorp mini II analyzer. The adsorbents were degassed in vacuum at 110 °C and kept overnight followed by further analysis28 (link). Smartsorb 92/93 surface area analyzer was used to assess the BET surface area of hydrochars. FTIR (Shimadzu’s 8400S model) was used to detect the molecular functionalities prevailing in the hydrochar at 400–4000 cm−1 wavenumber range29 (link). Horiba Scientific Nanopartica SZ-100 particle size analyzer was used to analyze the zeta potential of hydrochars30 . FEI—Quanta 250 Scanning Electron Microscope (SEM) was used to examine the structural morphologies of hydrochars at a voltage of 8 kV with × 10,000 magnification. FEI—Quanta 250 Transmission Electron Microscope (TEM) was used to interpret the hydrochar’s internal morphologies at an operating voltage 120 kV31 . The point of zero charge (pHzpc) was determined using pH drift method.
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3

Comprehensive Gas Adsorption Characterization

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N2 isotherms (up to P/P0 = 1 and 77 K) were recorded on a BELSORP mini
II analyzer under high vacuum in a clean system with a diaphragm pumping
system. CO2 isotherms (up to 1 bar and 196 K) were recorded
on a BELSORP HP (high-pressure) analyzer. Prior to measurement samples
were activated under vacuum (0.1 Pa) at 393 K for 1 h. Ethanol isotherms
were measured at 303 K by a gravimetric method in a DVS Advantage
1 apparatus from Surface Measurement System, UK. This instrument consists
of a Cahn microbalance (mass sensitivity: 0.1 μg), with a digital
optical microscope, set up in an exactly controlled temperature and
vapor pressure chamber (accuracy: 0.1 K and 0.7% P/P0; respectively). Dry, and high-purity
nitrogen was used as the carrier gas.
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4

Characterizing Char Porosity by N2 Adsorption

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The porosity of the chars obtained from different conditions was analyzed by the N2 adsorption–desorption technique. The char samples were outgassed at 300 °C for 3 h in a vacuum, and then introduced to the BELSORP-mini II analyzer to conduct N2 adsorption–desorption at 77 K. Data was obtained over the relative pressure range from 0 < p/p0 < 0.99. Based on the adsorption–desorption results, the Brunauer–Emmett–Teller (BET) method was applied to estimate the SSA and total pore volume of the chars, while micropore surface area and volume were estimated by the t-plot method.
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5

Comprehensive Characterization of Electrode Materials

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The microstructures and morphologies of the materials were studied on a eld emission scanning electron microscope (FESEM, Mira 3-XMU, TESCAN Co.). The crystal structure was evaluated on an X-ray diffraction (XRD) system (microanalyzerxmf-104) with Cu Kα radiation. Raman spectroscopy (Takram P50C0R10, Teksan) with a laser wavelength of 532 nm was used to characterize the degree of graphitization of electrodes. Thermogravimetric analysis (TGA) was conducted in the air over a temperature range of 50-800 °C with a heating rate of 10 °C min -1 using a STA 504. Nitrogen adsorption/desorption isotherms were obtained on a Belsorp mini II analyzer at 77 K. The speci c surface areas were determined using the Brunauer-Emmett-Teller (BET) method. The electrical conductivity of samples was measured based on the two -point probe methods (2602A system source meter, keithley) at room temperature.
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