Influence of Pressure Generation Rate on Both Pore Size Distribution Measured by Mercury Porosimetry and Predicted Permeability

2021 ◽  
Vol 62 (3) ◽  
pp. 170-180
Author(s):  
Wataru TANIKAWA ◽  
Osamu TADAI
Keyword(s):  
Pore Size Distribution ◽  
Pore Size ◽  
Size Distribution ◽  
Mercury Porosimetry ◽  
Generation Rate

scholarly journals Impact of Polymer Binders on the Structure of Highly Filled Zirconia Feedstocks

Polymers ◽  
2020 ◽  
Vol 12 (10) ◽  
pp. 2247
Author(s):  
Claire Delaroa ◽  
René Fulchiron ◽  
Eric Lintingre ◽  
Zoé Buniazet ◽  
Philippe Cassagnau
Keyword(s):  
Pore Size Distribution ◽  
Pore Size ◽  
Size Distribution ◽  
High Density Polyethylene ◽  
Mercury Porosimetry ◽  
High Density ◽  
Organic Binder ◽  
Molten State ◽  
Homogeneous Dispersion ◽  
The Impact

The impact of polypropylene and high-density polyethylene backbone binders on the structure of organic matrix, feedstock, and ceramic parts is investigated in terms of morphology in this paper. The miscibility of wax with polyethylene and polypropylene is investigated in the molten state via a rheological study, revealing wax full miscibility with high-density polyethylene and restricted miscibility with polypropylene. Mercury porosimetry measurements realized after wax extraction allow the characterization of wax dispersion in both neat organic blends and zirconia filled feedstocks. Miscibility differences in the molten state highly impact wax dispersion in backbone polymers after cooling: wax is preferentially located in polyethylene phase, while it is easily segregated from polypropylene phase, leading to the creation of large cracks during solvent debinding. The use of a polyethylene/polypropylene ratio higher than 70/30 hinders wax segregation and favors its homogeneous dispersion in organic binder. As zirconia is added to organic blends containing polyethylene, polypropylene, and wax, the pore size distribution created by wax extraction is shifted towards smaller pores. Above zirconia percolation at 40 vol%, the pore size distribution becomes sharp attesting of wax homogeneous dispersion. As the PP content in the organic binder decreases from 100% to 0%, the pore size distribution is reduced of 30%, leading to higher densification ability. In order to ensure a maximal densification of the final ceramic, polyethylene/polypropylene ratios with a minimum content of 70% of high-density polyethylene should be employed.

Demineralized dentin 3D porosity and pore size distribution using mercury porosimetry

2009 ◽  
Vol 25 (6) ◽  
pp. 729-735 ◽  
Author(s):  
Elsa Vennat ◽  
Christine Bogicevic ◽  
Jean-Marie Fleureau ◽  
Michel Degrange
Keyword(s):  
Pore Size Distribution ◽  
Pore Size ◽  
Size Distribution ◽  
Mercury Porosimetry ◽  
Demineralized Dentin

On the characterization of pore size distribution of building materials

2017 ◽  
Vol 41 (3) ◽  
pp. 247-263 ◽  
Author(s):  
LF Dutra ◽  
N Mendes ◽  
PC Philippi
Keyword(s):  
Relative Humidity ◽  
Pore Size Distribution ◽  
Pore Size ◽  
Size Distribution ◽  
Building Materials ◽  
Mercury Porosimetry ◽  
Energy Performance ◽  
Volume Distribution ◽  
Wide Range

Moisture affects significantly the energy performance of air conditioning systems, the durability of materials, and the health of occupants. One way of reducing those effects, without increasing the energy costs, is by means of using porous material ability of absorbing and releasing moisture from/to the adjacent environment, which attenuates the indoor relative humidity variation. This natural ability is intrinsically related to the porous microstructure. Therefore, the characterization of the pore space is an important research theme in the building physics area. This article aims to present a method for obtaining the pore size distribution based on adsorption isotherms and mercury porosimetry data. First, the theoretical formulation based on the Gibbs free energy for a two-phase (liquid–vapor) system, using the De Boer and Zwikker model, is presented, allowing the calculation of the critical adsorbed thickness for pore filling, critical radius, adsorbed moisture content, capillary condensation content, available surface for adsorption, and the distribution of micropores for a wide range of radius. The adsorption isotherm curve is estimated for high relative humidity values through mercury porosimetry, along with the adsorption curve obtained from the experiment. The pore volume distribution calculated by this method can be used to estimate transport coefficients for liquid and vapor phases.

Pore Structure Of Hydrated Cement Determined By Mercury Porosimetry And Nitrogen Sorption Techniques.

1988 ◽  
Vol 137 ◽  
Author(s):  
Yahia Abdel-Jawad ◽  
Will Hansen
Keyword(s):  
Pore Structure ◽  
Pore Size Distribution ◽  
Pore Size ◽  
Size Distribution ◽  
Pore Volume ◽  
Mercury Porosimetry ◽  
Total Pore Volume ◽  
Curing Temperature ◽  
Vycor Glass ◽  
Degree Of Hydration

AbstractThe pore structure (i.e. total pore volume, surface area and pore-size distribution curves) was measured using mercury porosimetry and nitrogen sorption. Hydrated portland cement (type I) of water-cement (w/c) ratios 0.3, 0.4 and 0.6 by weight was analyzed at three degrees of hydration (i.e., 30%, 50% and 80%; 70% for the 0.3 w/c system) corresponding to low, intermediate and high levels of hydration. The effect of curing temperature (3°, 23°, and 43°C) on pore structure was also studied. The two techniques were evaluated as well on porous Vycor glass, which has a narrow pore size distribution in the size range accessible to both. Results obtained by both techniques on porous Vycor glass agreed well. However neither technique can be used alone to study the entire pore structure in well-hydrated cement due to the wide range in pore sizes and the presence of micropores. Due to the unstable pore structure in cement a specimen treatment procedure such as methanol replacement, combined with volume-thickness (V-t) analysis, is necessary in order to measure the micropores. At low hydration values the pore structure can be estimated by mercury intrusion porosimetry (MIP). At higher hydration values, however, this technique underestimates total pore volume and surface area due to the presence of micropores which MIP cannot determine. In the pore size range of overlap, higher pore volumes were obtained with MIP. Nitrogen V-t analysis shows that micropores are more pronounced with lower w/c ratios. This finding is consistent with pore size distribution curves obtained by MIP. For a given w/c ratio and degree of hydration the total pore volume measured by MIP was found to be independent of curing temperature in the temperature range studied. At any w/c ratio, capillary porosity is controlled by degree of hydration alone.

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