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Autopore 9520

Manufactured by Micromeritics
Sourced in United States

The AutoPore 9520 is a mercury intrusion porosimeter designed for the measurement of pore size distribution and pore volume in solid materials. It provides detailed information about the porous structure of a wide range of materials, including catalysts, adsorbents, ceramics, and construction materials.

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7 protocols using autopore 9520

1

Comprehensive Material Characterization Techniques

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All Raman spectra, including the SERS analysis, were analyzed using Raman spectroscopy (HORIBA, Osaka, Japan, LabRAM HR-800). The laser power was 3 mW, the excitation wavelength was 532 nm, and a × 50 objective with NA = 0.5 was used. The morphological characteristics were analyzed by using a field-emission scanning electron microscopy (FE-SEM, HITACHI, Tokyo, Japan, S-4800) at 15 kV. Surface activation energy analyses were performed by using a water contact angle (WCA) analyzer (SEO, Phoenix MT, Seoul, Republic of Korea). Characterization of the pore distribution of the samples was performed using mercury intrusion porosimetry (Micromeritics, Norcross, GA, USA, AutoPore 9520).
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2

Comprehensive Material Characterization Techniques

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All Raman spectra, including the SERS analysis, were analyzed using Raman spectroscopy (HORIBA, Osaka, Japan, LabRAM HR-800). The laser power was 3 mW, the excitation wavelength was 532 nm, and a × 50 objective with NA = 0.5 was used. The morphological characteristics were analyzed by using a field-emission scanning electron microscopy (FE-SEM, HITACHI, Tokyo, Japan, S-4800) at 15 kV. Surface activation energy analyses were performed by using a water contact angle (WCA) analyzer (SEO, Phoenix MT, Seoul, Republic of Korea). Characterization of the pore distribution of the samples was performed using mercury intrusion porosimetry (Micromeritics, Norcross, GA, USA, AutoPore 9520).
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3

Characterization of Porous Cement Composites

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The pore structure was determined by mercury intrusion porosimetry (AutoPore 9520, Micromeritics, Norcross, GA, USA), in which the specimen was prepared by stopping the hydration reactions using acetone and an aspirator. A pressure ranging from 3.64 × 103 to 4.14 × 108 Pa was applied to the pores, corresponding to a maximum and minimum pore size of 340 μm and 3 nm, respectively. The mechanical strength was evaluated by measuring the compressive strength of the cubic specimens at a pressing speed of 4 mm/min. Impedance spectra were acquired using an impedance analyzer (SI 1260, Solartron, UK) with an oscillating voltage of 0.1 V between 10 MHz and 1 Hz. A stainless steel plate was employed as an electrode, and the distance between electrodes was 40 mm. A three-point bending test was used on the 3D-printed, beam-shaped specimens to evaluate mechanical tensile properties using a custom-made universal test machine at a pressing speed of 0.1 mm/min.
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4

Porosity Analysis of 3D-Printed Tablets

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A surface area and pore size analyzer (AutoPore 9520, Micromeritics, Atlanta, GA, USA) was used to determine the porosity of the 3D-printed compound LEV-PN multicompartmental dispersible tablets. The bulk density was measured at 0.22 PSIA, and the apparent density was measured at 29,995 PSIA. The pore size distribution, average pore size, and porosity were recorded. The porosity was calculated as follows:
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5

Characterizing Ionomer Membrane Porosity

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The pore size and pore distribution of the prepared CLs containing blended or single ionomers were measured using a pore characterization system (AutoPore 9520, Micromeritics, Norcross, GA, USA). The prepared CL-coated membranes were diced into several pieces of 1 cm2 until the total amount of all diced pieces was 0.5 g. The applied pressure range was 0 to 60,000 psia [36 (link)].
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6

Pore Size Distribution Analysis of Tablets

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The pore size distribution and average pore diameter of the tablets were measured by a surface area and pore size analyser (AutoPore 9520, Micromeritics, USA), and the bulk density and apparent (skeletal) density were measured at 0.21 psia and 29,996 psia, respectively. The porosity can be calculated as follows: Porosity (%) = (1-bulk density/apparent (skeletal) density) × 100%).
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7

Bentheimer Sandstone Core Preparation

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The rock sample we used in this study was Bentheimer sandstone with an average porosity of 0.24 (measured with Autopore 9520, Micromeritics). Cylindrical rock samples called cores with 6.1 mm diameter and length of approximately 26 mm were drilled from a larger cylinder of rock (38 mm diameter and 40 mm long). The larger sample containing predrilled small cores was then fully saturated with potassium iodide (KI) doped brine (see The details of this sample preparation protocol can be found in our previous study [34] (link).
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