• 대한화학회지
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• 제27권3호
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• pp.189-193
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• 1983

리튬동위원소의 분리 실험이 염산과 양이온 교환 수지를 사용하여 행하여졌다. 이 실험에서는 porous sulfonated styrene-divinylbenzene copolymer와 Dowex 50w-x8의 양이온 교환수지가 사용되었다. 리튬의 양은 원자 흡광 분석기를 사용하여 측정되었다. 리튬 동위 원소의 상대적 질량은 질량 분석기로 측정하였다. 동위 원소의 분리인자는 분별된 용출액의 동위 원소 조성으로 부터 계산되었다. 분리 인자의 값은 염산과 porous sulfonated styrene-divinylbenzene copolymer system에서 1.0020이었고, 염산과 Dowex 50w-x8 system에서 1.0011${\om}$0.0002이었다. 이와 같은 결과로부터 우리들은 분리 인자의 값이 Dowex 50w-x8에서 보다 porous sulfonated styrene-divinylbenzene copolymer에서 더 크게 나타남을 알 수 있었다.

• 대한기계학회:학술대회논문집
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• 대한기계학회 2004년도 춘계학술대회
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• pp.1225-1230
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• 2004

In this paper, the pressure drops were investigated according to the sintered porous wick structure in loop heat pipe(LHP) by theoretical analysis. LHP has the wick only in evaporator for the circulation of working fluid, so utilizes porous wick structure which pore diameter is very small for large capillary force. This paper investigates the effects of different parameters on the pressure drops of the LHP such as particle diameter of sintered porous wick, wick porosity, vapor line diameter, thickness of wick and heating capacity. Working fluid is water and the material of sintered porous wick is copper. According to the these different parameters, capillary pressure, pressure drop in wick were analized by theoretical design method of LHP.

• Journal of Pharmaceutical Investigation
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• 제40권4호
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• pp.231-236
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• 2010

This study was to fabricate the porous poly(lactide-co-glycolide) (PLGA) microparticles with anthocyanin (as a model antioxidant) for pulmonary drug delivery. The highly porous PLGA microparticles were prepared by the waterin-oil-in-water ($W_1/O/W_2$) multi-emulsion method, followed by the decomposition of ammonium bicarbonate (AB) in $W_1$ phase to the base of ammonia, carbon dioxide and water vapor at $50^{\circ}C$, making a porous structure in PLGA microparticles. Herein, hyaluronate (HA), a viscous polysaccharide, was incorporated in the porous microparticles for sustained anthocyanin release. In in vitro release studies, the anthocyanin release from the porous microparticles with HA continued up to 24 hours, while the porous microparticles without HA released 80 wt.% of encapsulated anthocyanin within 2 hours. In addition, these microparticle are expected to be effectively deposited at a lung epithelium due to its high porosity (low density) and avoid alveolar macrophage's uptake in the lung due to its large particle size. We believe that this system has a great pharmaceutical potential as a long acting antioxidant for relieving the oxidative stress in chronic obstructive pulmonary disease (COPD).

• 한국콘크리트학회:학술대회논문집
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• 한국콘크리트학회 2001년도 가을 학술발표회 논문집
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• pp.311-316
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• 2001

This study analyzed the influence of paste fluidity and vibration time for fundamental properties of porous concrete. Results of this study were shown as follows; 1) Even if target void ratio is same, void ratio and compressive strength of porous concrete is different according to w/c, paste flow and vibration time. So, In case of target void ratio, we must consider the influence of w/c, paste flow, and vibration time. 2) Though w/c and vibration time are same, as paste flow increase, all void ratio, continuous void ratio, and compressive strength decrease and difference between upper and lower void ratio increase. 3) Though w/c and paste flow are same, as vibration time increase, all void ratio and continuous void ratio decrease and difference between upper and lower void ratio increase. Also, compressive strength increase by 10 seconds and decease after 10 seconds. 4) As types of superplasticizer is different, all void ratio, continuous void ratio, and compressive strength are different. So, we must give consideration to paste fluidity and vibration time in order that increase of strength of porous concrete and distribution of uniform void.

• 한국분말재료학회지
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• 제24권6호
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• pp.472-476
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• 2017

Porous W-10 wt% Ti alloys are prepared by freeze-drying a $WO_3-TiH_2$/camphene slurry, using a sintering process. X-ray diffraction analysis of the heat-treated powder in an argon atmosphere shows the $WO_3$ peak of the starting powder and reaction-phase peaks such as $WO_{2.9}$, $WO_2$, and $TiO_2$ peaks. In contrast, a powder mixture heated in a hydrogen atmosphere is composed of the W and TiW phases. The formation of reaction phases that are dependent on the atmosphere is explained by a thermodynamic consideration of the reduction behavior of $WO_3$ and the dehydrogenation reaction of $TiH_2$. To fabricate a porous W-Ti alloy, the camphene slurry is frozen at $-30^{\circ}C$, and pores are generated in the frozen specimens by the sublimation of camphene while drying in air. The green body is hydrogen-reduced and sintered at $1000^{\circ}C$ for 1 h. The sintered sample prepared by freeze-drying the camphene slurry shows large and aligned parallel pores in the camphene growth direction, and small pores in the internal walls of the large pores. The strut between large pores consists of very fine particles with partial necking between them.

• 한국정밀공학회:학술대회논문집
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• 한국정밀공학회 2012년도 춘계학술대회 논문집
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• pp.353-354
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• 2012

• 한국전산유체공학회지
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• 제18권2호
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• pp.17-25
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• 2013

The process of flow through porous media is of interest a wide range of engineering fields and areas, and the importance of fluid flow with a change in phase arises from the fact that many industrial processes rely on these phenomena for materials process, energy transfer. Especially, the flow phenomena of cryogenic liquid subjected to evaporation is of interest to investigate how the cryogenic liquid behaves in the porous structure. In this study, thermo physical properties, morphological properties of the glass wool with different bulk densities in terms of its temperature-dependence and permeability behaviors under different applying pressure are discussed. Using the experimentally determined properties, characteristics of two main experimental results are investigated. In addition, simulation results are used to realize the cryogenic liquid's flow in porous media, and are compared with experimental results. By using the experimentally determined properties, more reasonable results can be suggested in dealing with porous media flow.

• 한국재료학회지
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• 제26권6호
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• pp.320-324
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• 2016

Porous SiC beads were prepared by freeze-drying a polycarbosilane (PCS) emulsion. The water-in-oil (w/o) emulsion, which was composed of water, PCS dissolved p-xylene, and sodium xylenesulfonate (SXS) as an emulsifier, was frozen by dropping it onto a liquid $N_2$ bath; this process resulted in 1~2 mm sized beads. Beads were cured at $200^{\circ}C$ for 1 h in air and heat-treated at $800^{\circ}C$ and $1400^{\circ}C$ for 1 h in an Ar gas flow. Two types of pores, lamella-shaped and spherical pores, were observed. Lamellar-shaped pores were found to develop during the freezing of the xylene solvent. Water droplets in the w/o emulsion were changed into spherical pores under freeze-drying. At $1400^{\circ}C$ of heat-treatment, porous SiC was synthesized with a low level of impurities.

• 한국분말야금학회:학술대회논문집
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• 한국분말야금학회 2006년도 Extended Abstracts of 2006 POWDER METALLURGY World Congress Part 1
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• pp.438-439
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• 2006

Pure and stable YAG $(Y_3Al_5O_{12})$ powders were synthesized by a PVA (polyvinyl alcohol) polymer solution technique. PVA was used as an organic carrier for the precursor ceramic gel. The precursor gels were crystallized to YAG at relatively a low temperature of $900\;^{\circ}C$. The synthesized powders, which have nano-sized primary particles, were soft and porous, and the porous powders were ground to sub-micron size by a simple ball milling process. The ball-milled powders were densified to 94% relative density at $1500\;^{\circ}C$ for 1h. In this study, the characteristics of the synthesized YAG powders were examined.

• 한국분말재료학회지
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• 제22권2호
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• pp.129-133
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• 2015

Porous W with controlled pore structure was fabricated by thermal decomposition and hydrogen reduction process of PMMA beads and $WO_3$ powder compacts. The PMMA sizes of 8 and $50{\mu}m$ were used as pore forming agent for fabricating the porous W. The $WO_3$ powder compacts with 20 and 70 vol% PMMA were prepared by uniaxial pressing and sintered for 2 h at $1200^{\circ}C$ in hydrogen atmosphere. TGA analysis revealed that the PMMA was decomposed at about $400^{\circ}C$ and $WO_3$ was reduced to metallic W at $800^{\circ}C$. Large pores in the sintered specimens were formed by thermal decomposition of spherical PMMA, and their size was increased with increase in PMMA size and the amount of PMMA addition. Also the pore shape was changed from spherical to irregular form with increasing PMMA contents due to the agglomeration of PMMA in the powder mixing process.