• Transactions of the Korean Society of Mechanical Engineers
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• v.12 no.4
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• pp.825-832
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• 1988

An experiment was performed to study the heat pipe phenomenon of porous media heated above at one-dimensional steady state for the range of heat flux, 300 W/ $m^{2}$ ~ 2000w/ $m^{2}$. Glass beads, sand, and copper particles were used as porous media and distilled water was used as a working fluid. Result of experiment shows that the length of the two-phase zone increases with the decreasing particle size for the same heat flux. At relatively lower heat flux the length of the two-phase zone increases with the increasing heat flux, which contradicts the result of earlier work. However, its length remains nearly constant when the heat flux increases above a certain value. The length of the two-phase zone is proportional to the product of the heat flux by the hydrostatic capillary height under the limited value on heat flux, that is, $l_{t}$ = A(q. $l_{cap}$)+B, q.leg.1/A(C+B/ $l_{cap}$) where A is 1.7*10$^{-4}$ $m^{2}$/w, B is 1.9*10$^{-2}$ m, and C is 0.43 for copper particles and 0.31 for glass beads and sand.d.d.d.

• Corrosion Science and Technology
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• v.9 no.5
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• pp.196-200
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• 2010

Recently porous metal has been used as supporting metal in planar type SOFC. In order to search optimum alloys for porous metal support and estimate the stability of metal-supported SOFC at high temperature, it is necessary to investigate the oxidation behaviors of porous material for metal support in comparison with dense material. Oxidation tests of porous and dense stainless steels were conducted at $600^{\circ}C$ and $800^{\circ}C$. Since the specific surface area of porous material is much larger than that of dense material, surface area should be considered in order to compare the oxidation rate of porous stainless steel with that of dense stainless steel. The specific surface area of porous body was measured using image analyzer. The weight gain of porous stainless steel was much greater than those of dense stainless steels due to its larger specific surface area. considering the specific surface area, the oxidation rate of porous stainless steel is likely to be the same as that of dense stainless steel with the same surface area. The change in chromium content in stainless steel during oxidation was also investigated. The experimental result in chromium content in stainless steel during oxidation corresponded with the calculated value. While the change in chromium content in dense stainless steel during oxidation is negligible, chromium content in porous stainless steel rapidly decreases with oxidation time due to its large specific surface area. The significant decrease in chromium content in porous stainless steel during oxidation may affect the oxidation resistance of porous stainless steel support and long term stability of metal-supported SOFC.

• Korean Journal of Materials Research
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• v.28 no.2
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• pp.108-112
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• 2018

The present study demonstrates the effect of raw powder on the pore structure of porous W-Ni prepared by freeze drying of camphene-based slurries and sintering process. The reduction behavior of $WO_3$ and $WO_3-NiO$ powders is analyzed by a temperature programmed reduction method in Ar-10% H2 atmosphere. After heat treatment in hydrogen atmosphere, $WO_3-NiO$ powder mixture is completely converted to metallic W without any reaction phases. Camphene slurries with oxide powders are frozen at $-30^{\circ}C$, and pores in the frozen specimens are generated by sublimation of the camphene during drying in air. The green bodies are hydrogen-reduced at $800^{\circ}C$ and sintered at $1000^{\circ}C$ for 1 h. The sintered samples show large and aligned parallel pores to the camphene growth direction, and small pores in the internal wall of large pores. The strut between large pores, prepared from pure $WO_3$ powder, consists of very fine particles with partially necking between the particles. In contrast, the strut densification is clearly observed in the Ni-added W sample due to the enhanced mass transport in activation sintering.

• Journal of ILASS-Korea
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• v.14 no.1
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• pp.20-27
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• 2009

In the present work, effects of spray characteristics (droplet size and velocity) on the temperature variation of a heated porous plate (Melamine foam) have been investigated through a series of experiments. Based on the measured data, time required to cool down the hot porous material turned out to be shorten by doing with the smaller droplet size and/or smaller impinging velocity. In particular, the droplet size effect is more prominent than the impinging velocity. The cooling performance in the porous material is directly proportional to the penetration velocity.

• Proceedings of the Korean Institute of Building Construction Conference
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• 2011.05a
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• pp.69-72
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• 2011

The purpose of this study is to identify basic property of porous concrete using cooper slag as fine aggregate. The specimens were made with cooper slag with various mixing ratio(10, 20, 30, 50%), porous concrete and porous concrete containing river fine aggregate and crushed fine aggregate, which W/B ratio fixed 0.25. Compressive strength, Flexural strength, coefficient of permeability. From the test results, various fine aggregate mixing ratio improves compressive strength and flexural strength, but cooper slag fine aggregate mixing ratio over 20%, concrete indicates trend to decrease performance of permeability. Concrete containing fine aggregate is improved the performance of permeability and strength compared to other specimen, when age 28days, and cooper slag mixing ratio less than 20% concrete indicates better performance than cooper slag mixing ratio 20% over.

• Journal of Integrative Natural Science
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• v.14 no.4
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• pp.147-154
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• 2021

A luminescent porous silicon sensor, whose surface was passivated with organic molecule via hydrosilylation under various conditions, has been researched to measure the photoluminescence (PL) stability of porous silicon (PSi). Photoluminescent PSi were synthesized by an electrochemical etching of n-type silicon wafer under the illumination with a 300 W tungsten filament bulb during the etching process. The PL of PSi displayed at 650 nm, which is due to the quantum confinement of silicon quantum dots in the PSi. To stabilized the photoluminescence of PSi, the hydrosilylation of PSi with silole molecule containg vinyl group was performed. Surface morphologies of fresh PSi and surface-modified PSi were obtained with a cold FE-SEM. Optical characterization of red photoluminescent silicon quantum dots was investigated by UV-vis and fluorescence spectrometer.

• Proceedings of the Korean Society for Technology of Plasticity Conference
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• 2003.10a
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• pp.359-362
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• 2003

Damping systems have been widely used to various industrial structures and are mainly hydraulic and pneumatic devices nowadays. In this work, a novel damping system based on the colloidal suspension in the field of nanotechnology is investigated. The colloidal suspension consists of Iyophobic working fluid and hydrophobic-coated porous particle. The mechanism of mechanical energy dissipation in damping system based on the colloidal suspension with nano-porous particles is different from that of the existing hydraulic damping system. The absorbed energy of the damping system using colloidal suspension can be calculated through the mechanical equilibrium condition by the superficial tensions of liquid-gas Interface in the hydrophobic surface in nano-porous particles. The results from an analytic approach have a reasonable agreement with experimental results.

• Proceedings of the Korean Society of Precision Engineering Conference
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• 2010.11a
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• pp.655-656
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• 2010

• Journal of Pharmaceutical Investigation
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• v.40 no.4
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• pp.245-250
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• 2010

Porous poly(lactic-co-glycolic acid) microspheres (PLGA MS) have been utilized as an inhalation delivery system and a matrix scaffold system for tissue engineering. Here, gelatin (type A) is introduced as an extractable pH-responsive porogen, which is capable of controlling the porosity and pore size of PLGA microspheres. Porous PLGA microspheres were prepared by a water-in-oil-in-water ($w_1/o/w_2$) double emulsification/solvent evaporation method. The surface morphology of these microspheres was examined by varying pH (2.0~11.0) of water phases, using scanning electron microscopy (SEM). Also, their porosity and pore size were monitored by altering acidification time (1~5 h) using a phosphoric acid solution. Results showed that the pore-forming capability of gelatin was optimized at pH 5.0, and that the surface pore-formation was not significantly observed at pHs of < 4.0 or > 8.0. This was attributable to the balance between gel-formation by electrostatic repulsion and dissolution of gelatin. The appropriate time-selection between PLGA hardening and gelatin-washing out was considered as a second significant factor to control the porosity. Delaying the acidification time to ~5 h after emulsification was clearly effective to make pores in the microspheres. This finding suggests that the porosity and pore size of porous microspheres using gelatin can be significantly controlled depending on water phase pH and gelatin-removal time. The results obtained in this study would provide valuable pharmaceutical information to prepare porous PLGA MS, which is required to control the porosity.

• Journal of Pharmaceutical Investigation
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• v.39 no.3
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• pp.167-171
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• 2009

Poly(lactic-co-glycolic acid) (PLGA) microspheres have been a useful tool as a controlled drug delivery system for peptides and proteins. Recently, porous microspheres have gained great attention as inhalation drug delivery system due to their low aerodynamic densities. Here, we report highly porous PLGA microspheres, which were prepared by using a single o/w emulsification/solvent evaporation method. Two types of porogen, i.e., (i) extractable Pluronic F127 and (ii) gas foaming salt of ammonium bicarbonate, were used to induce pores on the surface of PLGA microspheres. The respective preparation conditions on dp/cp ratio and porogen concentration were determined by the previous preliminary experiments, and other preparation factors were further optimized on the basis of PLGA Mw and porogen type. The morphological features examined by scanning electron microscope (SEM) show these porous microspheres have highly porous surface structure with a diameter range of 20${\sim}$30 ${\mu}$m. These highly porous PLGA microspheres, which have much lower density, would be a practical aerosol system for pulmonary drug delivery.