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Autopore 9500

Manufactured by Micromeritics
Sourced in United States

The AutoPore 9500 is a laboratory instrument designed for high-pressure mercury intrusion porosimetry. It measures the pore size distribution and total pore volume of materials by intruding mercury into the sample under pressure. The instrument can reach pressures up to 60,000 psia (414 MPa), allowing for the characterization of pores as small as 3 nanometers in diameter.

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9 protocols using autopore 9500

1

Characterizing Macroporous Materials via MIP

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MIP
is a widely used technique that allows the characterization of macropores
(>50 nm) in porous materials. Here, MIP measurements were conducted
with the Autopore 9500 manufactured by the Micromeritics Company,
USA, with a maximum intrusion pressure of 220 MPa. The samples (approximately
0.8 g, 60–80 mesh) were dried at 105 °C for 6 h before
testing. In each measurement, the test was performed in two stages.
The first stage is the low-pressure stage with a pressure range of
0–0.14 MPa. The second stage is the high-pressure stage with
a pressure range of 0.14–210 MPa. The MIP data were related
to the pore structure through the Washburn equation.33 (link),39 (link) The MIP measurements were repeated thrice, and the final results
were the averages of the three independent results.
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2

Mercury Porosimetry of BMCS

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The porous structure of the BMCS, such as pore volume (PV) and porosity were measured by an AutoPore-9500 mercury porosimeter (Micromeritics Instrument Ltd., United States) using a powder sample tube with the pressure ranges from 0.52 Pisa to 60,000 Pisa (corresponding to a pore size range of 347,263–3 nm) and an equilibrium time of 10 min.
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3

Comprehensive Characterization of Geopolymers

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The chemical analysis of CG, FA and BFS was performed by an X-ray fluorescence instrument (Axios Advanced, Almelo, The Netherlands). The structure and composition of CG were tested by the Brucker D8 X-ray diffraction meter (Karlsruhe, Germany). The FTIR spectrometer of Vector-22 Bruker from Germany was employed to analyze the evolution of changes before and after adsorption of geopolymers. The pore sizes of geopolymers were reported by a mercury injection apparatus (AutoPore 9500, Micromeritics Instrument Corporation, Knoxville, TN, USA). The surface structure of the geopolymers was characterized by SEM (Quanta 250, FEI Company, Peabody, MA, USA) at an accelerating voltage of 0.2–30 kV. Samples were sputtered with gold before the SEM measurements. Changes of binding energy before and after adsorption were obtained by X-ray photoelectron spectrometer (ESCALAB 250, Thermo Fisher Scientific, Waltham, MA, USA) at 0.6 eV energy resolution. The electrokinetic properties of the geopolymers were measured by a Zetasizer Nano-ZS90 instrument (Malvern Panalytical, Malvern, UK) with electrophoretic light-scattering technology.
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4

Characterization of Novel Monolithic Sorbent

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The photo-initiated copolymerization of SBVI was carried out using UV light at 254 nm and 50 Hz (ALYS Labware, Lausanne, Switzerland). A Zeiss ULTRA 55 field-emission scanning electron microscope (Oberkochen, Germany) was employed for scanning electron microscopy (SEM) and energy-dispersive X-ray spectrometry (EDS) tests of the novel monolith at acceleration voltages of 5 and 15 kV, respectively. A Micromeritics Auto Pore 9500 automatic mercury porosimeter (Norcross, GA, USA) was used to measure pore size distribution. The zeta potential of the resulting monolith was measured using a Malvern Nano-ZS ζ-potential meter (Malvern Panalytical, Malvern, UK). An inverted fluorescence microscope (Olympus, Tokyo, Japan) was used to evaluate the adsorption of FITC-labeled BSA on the monolith. Moreover, the adsorbed protein amount was tested using a Synergy LX microplate reader (BioTek, Winooski, VT, USA). Matrix assisted laser desorption ionization time of flight mass spectrometry (MALDI-TOF MS) analysis was performed using a Bruker UltrafleXtreme MALDI TOF/TOF mass spectrometer (Bruker Daltonics, Billerica, MA, USA) to identify the enriched N-glycopeptides. Only peptides containing the Asn-X-Ser/Thr/Cys sequence (X is any amino acids other than Pro) were identified as N-glycopeptides.
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5

Microstructure and Porosity of Cement Paste

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The microstructure of the cement pastes was investigated using field emission scanning electron microscopy (SEM, JSM-7600F, Japan). SEM was carried out on the fractured surface of the cement paste after mechanical testing. Prior to the measurement, samples were soaked in anhydrous ethanol for 48 h and then dried at 60°C in a vacuum oven for 48 hrs. The specimens were mounted on aluminum stubs with conductive carbon tape and sputtered with gold under vacuum at 20 mA for 2 min.
The porosity of cement paste composites was examined as follows. The pore volume and pore size analysis were performed on a mercury intrusion porosimeter (Micromeritics AutoPore 9500, America). The specimens were intruded with mercury and the quantity and pressure required for the intrusion were used to calculate the sizes and amount of pores within the sample according to the Washburn equation:
r=2rcosθp
where r is the pore radius (μm), γ is the surface tension of mercury (480 mN/m), θ is the contact angle between mercury and probe wall (140° as recommended by the manufacturer of the porosimeter), and P is the applied pressure (MPa) [54 ]. Three repeated measurements were conducted for each test.
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6

Comprehensive Material Characterization of LTA-type Zeolite

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An X-ray diffractometer (XRD, SmartLab; Rigaku
Corp.) was used for
structural analyses. Dynamic light scattering spectroscopy (DLS, ELS-Z;
Otsuka Electronics Co., Ltd.), scanning electron microscopy (SEM,
S-4800; Hitachi High-Technologies Corp.), and transmission electron
microscopy (TEM, TECNAI G2; FEI Co.) were used to analyze the particle
size and shape. The water vapor adsorption isotherm and the nitrogen
adsorption isotherm were obtained, respectively, from the following
apparatus: BELSORP-aqua3 and BELSORP MAX (MicrotracBEL Corp.). Mercury
porosimetry (Autopore 9500; Micromeritics Instrument Corp.) was conducted
to analyze the size distribution of mesopores and macropores in the
LTA-type zeolite sample. In addition, a sine-wave vibro viscometer
(SV-10A; A&D Co. Ltd.) was used to measure the LTA-type raw material
slurry viscosity.
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7

Soil Pore Size Distribution Analyzed

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Samples of 1 g dry soils (sandy-loam, loam and clay-loam) were mixed with the mucilage at 2% w/w. Distilled water was added to bring soil samples to 30% of field capacity (Traoré et al., 2000) and left stand for 72 h. Control soil samples (without mucilage) were treated in the same way.
The distribution of pore radii of soil samples from 4 × 10 4 to 3.7 nm was determined using a mercury depression and intrusion porosimeter Autopore 9500 produced by Micromeritics, and instructions given by manufacturer. Small pieces of undisturbed soil aggregates were heated at 90 °C during 24 h and then outgassed at room temperature for 30 min before each experiment. A value for the surface tension of mercury of 0.48 N m -1 and a contact angle on soils of 141.3°were used with the Laplace equation assuming cylindrical pores in the calculations.
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8

Characterization of Fiber-Mortar Interface

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Cubic samples with a side length of ≤8 mm were cut from the cured specimens and dried in the oven at 50 °C for one week. The pore structure was measured using mercury intrusion porosimetry (AutoPore 9500, Micromeritics, USA). To observe the fiber–mortar interface, the block samples were firstly cut from the mortar specimens, and also dried at 50 °C for one week. After that, the sample surface was sprayed with gold to increase the conductivity, then the micromorphology of the fiber–mortar interface was obtained using scanning electron microscope (Sigma500, ZEISS, Germany).
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9

Mercury Intrusion Porosimetry of MKPC

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Mercury, which is not infiltrated into general solids, can enter the hole by applying external pressure. The larger the external pressure, the smaller the diameter of the hole into which mercury can enter. The volume of the pore is judged by measuring the amount of mercury entering the pore under different external forces. In this paper, mercury pressure experiments were performed on MIP samples in order to evaluate the pore structure of MKPC by the AutoPore 9500 (Micromeritics, Norcross, GA, USA).
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