Microstructure characterization of mullite foam by image analysis, mercury porosimetry and X-ray computed microtomography
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F18%3A43916701" target="_blank" >RIV/60461373:22310/18:43916701 - isvavai.cz</a>
Výsledek na webu
<a href="https://www.sciencedirect.com/science/article/pii/S0272884218308769" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0272884218308769</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.ceramint.2018.04.019" target="_blank" >10.1016/j.ceramint.2018.04.019</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Microstructure characterization of mullite foam by image analysis, mercury porosimetry and X-ray computed microtomography
Popis výsledku v původním jazyce
It is well known that the effective properties of porous ceramics and ceramic foams depend strongly on the microstructure. That means, the prediction of effective properties of real materials generally requires quantitative values of well-defined microstructural descriptors as input parameters. The present contribution shows that ceramic foams with hierarchical microstructure require a complex microstructural characterization procedure based on a combination of different complementary techniques. Taking a light-weight mullite foam - an important and versatile ceramic material (e.g. for furnace linings, kiln furniture and high-temperature filters) - as a paradigmatic example, a systematic methodology is proposed for extracting relevant microstructural information. The microstructure of mullite foam with hierarchical microstructure has been characterized by stereology-based image analysis, mercury porosimetry and computed microtomography (X-ray mu CT). Three metric descriptors (porosity, surface density, mean curvature integral density) and a topological descriptor (Euler characteristic density) have been determined, the latter being 192.4 +/- 17.7.10(-9) mu m(-3). SEM micrographs taken at different magnification allow to distinguish the porosity attributable to pore cavities (62.3-63.0%) and matrix (47.8-49.5%). Mean chord lengths and Jeffries sizes of the pores are 159-164 mu m and 164-180 mu m, respectively, for the pore cavities and 4.6-5.1 mu m and 4.9-5.1 mu m, respectively, for the matrix pores. Different types of pore size distributions have been determined, and it is found that in this specific case the size distribution of pore cavity sizes obeys a Rayleigh distribution. Mercury porosimetry covers small and medium-sized pore throats (median 76 mu m), whereas image analysis captures pore cavities (median 234-247 mu m) and X-ray mu CT combines information on both pore throats and cavities, resulting in an intermediate median of 206 mu m. The procedure proposed is very general and systematic and can be applied to porous materials with a wide range of microstructures.
Název v anglickém jazyce
Microstructure characterization of mullite foam by image analysis, mercury porosimetry and X-ray computed microtomography
Popis výsledku anglicky
It is well known that the effective properties of porous ceramics and ceramic foams depend strongly on the microstructure. That means, the prediction of effective properties of real materials generally requires quantitative values of well-defined microstructural descriptors as input parameters. The present contribution shows that ceramic foams with hierarchical microstructure require a complex microstructural characterization procedure based on a combination of different complementary techniques. Taking a light-weight mullite foam - an important and versatile ceramic material (e.g. for furnace linings, kiln furniture and high-temperature filters) - as a paradigmatic example, a systematic methodology is proposed for extracting relevant microstructural information. The microstructure of mullite foam with hierarchical microstructure has been characterized by stereology-based image analysis, mercury porosimetry and computed microtomography (X-ray mu CT). Three metric descriptors (porosity, surface density, mean curvature integral density) and a topological descriptor (Euler characteristic density) have been determined, the latter being 192.4 +/- 17.7.10(-9) mu m(-3). SEM micrographs taken at different magnification allow to distinguish the porosity attributable to pore cavities (62.3-63.0%) and matrix (47.8-49.5%). Mean chord lengths and Jeffries sizes of the pores are 159-164 mu m and 164-180 mu m, respectively, for the pore cavities and 4.6-5.1 mu m and 4.9-5.1 mu m, respectively, for the matrix pores. Different types of pore size distributions have been determined, and it is found that in this specific case the size distribution of pore cavity sizes obeys a Rayleigh distribution. Mercury porosimetry covers small and medium-sized pore throats (median 76 mu m), whereas image analysis captures pore cavities (median 234-247 mu m) and X-ray mu CT combines information on both pore throats and cavities, resulting in an intermediate median of 206 mu m. The procedure proposed is very general and systematic and can be applied to porous materials with a wide range of microstructures.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
20504 - Ceramics
Návaznosti výsledku
Projekt
<a href="/cs/project/GA15-18513S" target="_blank" >GA15-18513S: Příprava a charakterizace oxidové a silikátové keramiky s řízenou mikrostrukturou a modelování souvislostí mezi mikrostrukturou a vlastnostmi</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2018
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Ceramics International
ISSN
0272-8842
e-ISSN
—
Svazek periodika
44
Číslo periodika v rámci svazku
11
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
14
Strana od-do
12315-12328
Kód UT WoS článku
000436351700051
EID výsledku v databázi Scopus
2-s2.0-85045089623