• Carbon letters
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• v.8 no.1
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• pp.17-24
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• 2007

Microporous carbons with narrow pore size distribution have been successfully synthesized by using hydrolyzed and calcined silica as templates and phenol formaldehyde (pf) resin as carbon precursor. Phenol formaldehyde-silica micro composites were prepared by solution route. Subsesequently, silica templates were removed by HF leaching. Resulting carbons were steam activated. The porous carbons were characterized by nitrogen adsorption-desorption isotherm, SEM, FTIR analysis, iodine adsorption, thermogravimetry analysis, etc. Adsorption isotherms show that the porous carbon prepared from calcined silica as templates are microporous with 88% pores of size <2 nm porosity and are of type I isotherm, while porous carbon prepared by using hydrolyzed silica are microporous with 89% microporosity, shows hysteresis loop at high relative pressure indicating the presence of some mesoporosity in samples. The microporosity in porous carbon materials has a bearing on the nature of silica templates used for pore formation.

• Journal of the Korean Ceramic Society
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• v.25 no.2
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• pp.89-94
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• 1988

Alumina gel was prepared by the hydrolysis of aluminum isopropoxide Al(OC3H7i)3 at low temperature. Sample were calcined at the various temperatures for 10 houres in the electric furnace, respectively. In order to investigate the various propertis-thermal properties, pore size and distribution, and the transition of crystals, infrared spectroscopy, thermal analysis, particle size analysis, scanning electron microscopy, and porosimetry were employed. Transparent alumina gel was opalized at 1200$^{\circ}C$. Porosity was about 87% with pores below 0.7$\mu\textrm{m}$ and 55% at 1200$^{\circ}C$. The gel was transformed along the rising of temperature as follows; Boehmite\longrightarrow$\delta$-Al2O3\longrightarrow$\theta$\longrightarrowAl2O3\longrightarrow${\alpha}$-Al2O3.

• Journal of the Korean Ceramic Society
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• v.25 no.6
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• pp.593-600
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• 1988

The properties of 10 kinds of MgO clinker were investigated to know the effect of MgO clinker's porperties on corrosion of MgO-C brick. For MgO clinker, chemical composition, porosity, density, periclase grain size, and microstructure were examined, while slag corrosion resistance was examined for MgO-C brick. In MgO clinker pore size and it's distribution, periclase grain size, impurities composition and the composition of grain boundaries are more important factors to determine corrosion degree of MgO-C brick than density, potosity and MgO purity.

• Proceedings of the Korean Institute of Building Construction Conference
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• 2015.05a
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• pp.23-24
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• 2015

As this study is an experiment for solving problem on the carbonation acceleration of high volume admixture concrete, the capillary pore getting filled up by saponification as cooking oil gets absorbed to the concrete surface in case of applying a cooking oil based coating agent to the concrete has been verified in the previous studies. Accordingly, this study has performed a comparative experiment on the cooking oil and the anticorrosive coating agent sold on the market while the result followed by this experiment has shown the fact of indicating similar carbonation penetration depth and porosity.

• Bulletin of the Korean Chemical Society
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• v.24 no.10
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• pp.1437-1443
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• 2003

Thermal decomposition of hydrated surface layer of $Mg(OH)_2$ at $500^{\circ}C$ in vacuum turned non-porous MgO into porous one with high surface area of around $270 m^2$/g. Most of its surface area, 74 %, was from micropores, and rest of it was from mesopores in wedge-shaped slits, exhibiting bimodal size distribution centered around 30 and 90${\AA}$. Rehydration followed by subsequent dehydration at $300 ^{\circ}C$ in dynamic vacuum further raised the surface area to 340 $m^2$/g. Fraction of microporous surface area was increased to 93%, and the shape of the mesopores was modified into parallel slits with a specific dimension of 32 ${\AA}$. Application of $Fe_2O_3$ over MgO via iron complex formation did not alter the pore characteristics of MgO core, except slightly increased pore dimension. Over the course of the modification, $Fe_2O_3$ stayed on the surface possibly via spill-over reaction.

• YAKHAK HOEJI
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• v.18 no.4
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• pp.236-242
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• 1974

Extrusion-spheronization processing combination was used to produce spherical granules with experimental formulations which contain microcrystalline cellulose as a diluent. The produced granules were compared on the basis of the following physical properties ; (a) bulk density, (e) porosity, (f) friabillity and (g) dissolution rate. With the specific experimental formulations used in this study, the increased plate rotational speeds of Marumerizer (400-1200rpm) produced continually more spherical material and also the obtained data indicated that the particle size distribution and dissolution rate depend upon the amount of microcrystalline cellulose used. As a result, the spherical granule preparation with microcrystalline cellulose has good properties in flow rate, packing propertyu and friability and offers a suitable method of granule preparation in pharmaceutical industry.

• Archives of Pharmacal Research
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• v.2 no.1
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• pp.17-24
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• 1979

A first systematic approach on new and simple preparation method of spherical granules in the system using organic granulating solution was carried out. Mixer granulation required narrow range of moisture content but gentle action of tumbling in the mixer and capilary forces were adequate to compact the porous mass and also were highly effective to produce granules close to sphere. Where the granules by massing and screening provided the more open structure, its pore distribution lied between 71 and 16 .mu.m by above 50% and on the contrary, that of the mixer granulated granules showed only below 25%. Increase in retention time in the mixer decreased the intragranular porosity of granules produced, and in comparison with granular particles produced by conventional wet granulation, those from the mixer granulation had the advantages of flow properties, packing characteristics and definite spherocity. They also had extremely low friability resulting in few fines.

• Journal of the Korean Ceramic Society
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• v.31 no.4
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• pp.407-414
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• 1994

Compacts were prepared using the SHS(Self-propagating High-temperature Synthesis) method and nitrided at temperatures range from 145$0^{\circ}C$ to 175$0^{\circ}C$, and pressed at 180$0^{\circ}C$ under N2 atmosphere. The samples were characterized for bulk density, porosity, pore size and distribution, phase composition, microstructure and fracture toughness. Compacts were composed of whiskers, which showed a good candidate for the composite materials. The major phases of the compacts nitrided at 175$0^{\circ}C$ and pressed at 180$0^{\circ}C$ were 15R-sialon with a large aspect ratio.

• Journal of the Korean Ceramic Society
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• v.49 no.6
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• pp.566-574
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• 2012

Porous zirconia ceramics are widely considered to be important due to their unique properties and potential applications. In this paper, we propose a novel approach to produce porous zirconia ceramics. The linear shrinkage of the prepared porous zirconia ceramics could be controlled to 4% by incorporating pre-sintered zirconia granules and hollow polymeric spheres. We also investigated the effect of pre-sintered zirconia granules on the microstructure and the properties, such as the porosity, pore distribution, and bending strength of the porous zirconia ceramics.

• Proceedings of the Korean Powder Metallurgy Institute Conference
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• 2006.09a
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• pp.509-510
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• 2006

Correlations between in-flight particle, splat and coating microstructure of thermally sprayed Ni20Cr were investigated. Flame spray and arc spray systems were employed for spraying Ni20Cr powder and Ni20Cr wire, respectively. The results showed that the arc spray process produced a broader size distribution for both in-flight particles and splats compared to flame process. Flower-like splat morphology was obtained from the arc spray whereas a pancake-like splat was obtained by flame spray. Ni20Cr coating sprayed by arc process had a denser microstructure, lower porosity and better adhesion at the interface.