• 멤브레인
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• 제15권1호
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• pp.52-61
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• 2005

폴리에틸렌 정밀여과 모세관막을 이용한 벤토나이트 콜로이드 현탁액의 투과유속 감소특성을 검토하였다. 운전시간이 경과하면서 투과유속이 감소되는 원인은 막표면 위에서 케익층의 성장과 입자들에 의한 세공막힘 때문이었으며, 운전시간이 경과하여 정상상태에 도달하면 투과유속은 케익여과 모델에 의해 지배받는다. 운전압력이 높은 경우의 투과유속 감소는 세공막힘과 케익층이 치밀해졌기 때문이다. 운전압력이 증가함에 따라 J/J₁는 감소하였으며, 0.5 kg/sub f//㎠일 때의 45%, 2.0 kg/sub f//㎠일 때 38%로 감소하였다. 운전압력 0.5 kg/sub f//㎠에서 총 막오염에 대한 성분오염의 비율은 표준세공막힘 14.6%, 완전세공막힘 23.4% 그리고 케익여과 62.0% 이었다. 순환흐름속도의 증가로 인해 투과유속은 증가하였고, 그 효과는 운전압력이 1.0 kg/sub f//㎠일 때가 운전압력 2.0 kg/sub f//㎠ 경우보다 컸다. 세공크기가 0.34 ㎛인 막의 투과유속은 세공의 크기가 0.24 ㎛인 막보다 컸으며, 용액의 농도에 따른 투과유속은 농도가 낮은 용액이 컸다. 세공크기가 0.34 ㎛인 막의 막오염 형태는 유사하지만 농도가 200 ppm인 용액의 경우 1000 ppm인 용액에 비하여 상대적으로 미약한 세공막힘 현상을 보였다.

• 한국토양비료학회지
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• 제40권3호
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• pp.189-195
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• 2007

Riew와 Sposito의 차원 분열 모델을 적용하여 토양과 상토를 대상으로 다공성 매체의 공극 분포와 보수력 비교를 시도하였다. 토양 시료는 라이시메터에서 2" 코아로 채취하였다. 상토 시료는 코코피트, 제올라이트 및 펄라이트를 혼합하여 아크릴 코아(100 mL)에 충진하여 조제하였다. 식 D=log(N)/log(1/r)를 포함한 차원 분열 모델에 의한 계산 Excell 프로그램을 작성하고, 이에 의해 분획된 다공성 매질을 이루는 보다 작은 크기(부피)의 매질 분획 상수인 N 값과 자기유사 비율 r 값을 얻었다. 이에 의해 대상 토양과 상토의 공극 분포와 빈도에 대한 자료를 얻을 수 있었다. 그 결과 라이시메타 토양은 상토 보다 더 넓은 공극 분포를 갖으며, 이에 비해 평균 공극크기는 상토 보다 라이시메타 토양에서 적은 것으로 해석되었다. 또한 공극크기(${\gamma}$) 분포에 따른 토양, 상토의 보수력은 토양은 상당한 단계의 토양수분이 빠져 나갔을 때 포장용수량(FC, 30kPa) 상태에 이르고, 상토는 비교적 적은 단계에서 포장용수량에 이르는 것으로 나타났다.

• 한국재료학회지
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• 제23권12호
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• pp.722-726
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• 2013

Freeze drying of a porous Cu-Sn alloy with unidirectionally aligned pore channels was accomplished by using a composite powder of CuO-$SnO_2$ and camphene. Camphene slurries with CuO-$SnO_2$ content of 3, 5 and 10 vol% were prepared by mixing with a small amount of dispersant at $50^{\circ}C$. Freezing of a slurry was done at $-25^{\circ}C$ while the growth direction of the camphene was unidirectionally controlled. Pores were generated subsequently by sublimation of the camphene during drying in air for 48 h. The green bodies were hydrogen-reduced at $650^{\circ}C$ and then were sintered at $650^{\circ}C$ and $750^{\circ}C$ for 1 h. XRD analysis revealed that the CuO-$SnO_2$ powder was completely converted to Cu-Sn alloy without any reaction phases. The sintered samples showed large pores with an average size of above $100{\mu}m$ which were aligned parallel to the camphene growth direction. Also, the internal walls of the large pores had relatively small pores. The size of the large pores decreased with increasing CuO-$SnO_2$ content due to the change of the degree of powder rearrangement in the slurry. The size of the small pores decreased with increase of the sintering temperature from $650^{\circ}C$ to $750^{\circ}C$, while that of the large pores was unchanged. These results suggest that a porous alloy body with aligned large pores can be fabricated by a freeze-drying and hydrogen reduction process using oxide powders.

• 한국결정성장학회지
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• 제7권1호
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• pp.174-184
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• 1997

야자각탄으로부터 수증법을 이용하여 활성탄을 제조하였다. 활성화 온도와 시간, 수증기의 농도와 양이 n-butane 흡착특성에 미치는 영향을 비표면적, 기공분석, n-butane 흡착량을 측정함으로서 분석하였다. 90$0^{\circ}C$ 이하에서 활성화한 경우 온도와 시간이 증가하거나 수증기의 농도와 양이 많을수록 n-butane 흡착량은 증가하였으나 95$0^{\circ}C$에 이르면 이러한 경향은 나타나지 않았다. $900^{\circ}C$, 185분간 활성화한 시료는 비표면적 978 $\textrm{m}^2$/g, 평균기공 크기 9.3 $\AA$, n-butane 흡착랑이 5.9 g/100 ml이었다.

• 한국염색가공학회지
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• 제11권5호
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• pp.22-29
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• 1999

The increase in color depth of polyester fiber dyed with black disperse dyes was investigated with respect to the kinds of resins and alkali treatment. The color depth of the dyed polyester fiber increased continuously according to the concentration of resins coated onto the fabrics. The alkali treatment to polyester fiber before dyeing also enhanced the color depth. It was thought that the polyester fiber was hydrolyzed by alkali resulting micropores on the sample. And the following treatment with a resin, Jet Black T-101, to the polyester fiber increased the color depth much higher. The successive process of alkali treatment, dyeing and Jet Black T-101 treatment could give the best color depth to polyester fiber. Although the alkali treatment reduced the tensile strength of polyester fiber, the color depth of polyester fiber enhanced sufficiently within the range of practically acceptable weight loss and strength. To analyze the micropore on the polyester fiber formed by alkali treatment, nitrogen porosimeter was used. As the weight loss of polyester fiber treated with alkali increased, the BET(Brunauer-Emmett-Teller) surface area, total pore volume, and average pore size of the sample increased.

• 한국수소및신에너지학회논문집
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• 제32권6호
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• pp.442-454
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• 2021

The porous transport layer (PTL) is essential to effectively remove oxygen and hydrogen gas from the electrode surface at high current density operation conditions. In this study, the effect of PTL with different characteristics such as pore size, pore gradient, interfacial coating was investigated by multi-layered sintered mesh. A water electrolysis single cell of active area of the 34.56 cm² was constructed, and IV performance and impedance analysis were conducted in the range of 0 to 2.0 A/cm². It was confirmed that the multi-layered sintered mesh PTL, which have an average pore size of 25 to 57 ㎛ and a larger pore gradient, removed bubbles effectively and thus seemed to improve IV performance. Also, it was confirmed that the catalytic metals such as Ni, NiMo coating on the PTL reduced activation overpotential, but increased mass transport overpotential.

• 한국건설순환자원학회논문집
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• 제6권3호
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• pp.118-125
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• 2011

콘크리트 내부의 공극의 크기 및 분포상태는 콘크리트의 내구성을 결정하는 요인 중 하나이며, 구조물의 성능을 판단하는데 중요한 지표로 사용된다. 최근 고유동 콘크리트(High-Fluidity Concrete 이하 HFC로 약함)에 대한 연구는 많은 시공사례와 함께 진행되고 있지만, 콘크리트의 내구성능에 영향을 미치는 공극구조에 대한 연구는 미비한 실정이다. 따라서 본 연구에서는 30 MPa 범위의 일반콘크리트(Conventional Concrete 이하 CC로 약함) 및 석회석 미분말 및 플라이 애시를 사용한 HFC를 제조하여 콘크리트의 공극구조를 비교 분석 하였다. 실험결과 30 MPa 범위의 CC 및 HFC의 평균 공극 직경은 HFC가 CC보다 작게 나타났으며, SEM 분석 결과 HFC가 CC보다 전체적으로 내부구조가 치밀한 것으로 나타났다. 이러한 결과를 통하여 HFC가 CC보다 내구성 측면에서 우수할 것으로 판단된다.

• 한국재료학회지
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• 제24권6호
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• pp.310-318
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• 2014

In this experiment, a highly porous scaffold of biphasic calcium phosphate (BCP) was prepared using the spongereplica method. The BCP scaffold was coated with 58S bioactive glass (BG) and sintered for a second time. The resulting scaffold was coated with gelatin (Gel) and cross-linked with [3-(3-dimethyl aminopropyl) carbodiimide] and N-Hydroxysuccinamide (EDC-NHS). The initial average pore size of the scaffold ranged from 300 to $700{\mu}m$, with more than 85 % porosity. The coating of BG and Gel had a significant effect on the scaffold-pore size, decreasing scaffold porosity while increasing mechanical strength. The material and surface properties were evaluated by means of several experiments involving scanning electron microscopy (SEM), energy-dispersive X-ray (EDX) and X-ray diffraction (XRD). Cytotoxicity was evaluated using MTT assay and confocal imaging of MC3T3-E1 pre-osteoblast cells cultured in vitro. Three types of scaffold (BCP, BCP-BG and BCP-BG-Gel) were implanted in a rat skull for in vivo evaluation. After 8 weeks of implantation, bone regeneration occurred in all three types of sample. Interestingly, regeneration was found to be greater (geometrically and physiologically) for neat BCP scaffolds than for two other kinds of composite scaffolds. However, the other two types of scaffolds were still better than the control (i.e., defect without treatment).

• 한국재료학회지
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• 제21권1호
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• pp.21-27
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• 2011

A nano-porous structure of tin oxide was prepared using an anodic oxidation process and the sample's electrochemical properties were evaluated for application as an anode in a rechargeable lithium battery. Microscopic images of the as-anodized sample indicated that it has a nano-porous structure with an average pore size of several tens of nanometers and a pore wall size of about 10 nanometers; the structural/compositional analyses proved that it is amorphous stannous oxide (SnO). The powder form of the as-anodized specimen was satisfactorily lithiated and delithiated as the anode in a lithium battery. Furthermore, it showed high initial reversible capacity and superior rate performance when compared to previous fabrication attempts. Its excellent electrode performance is probably due to the effective alleviation of strain arising from a cycling-induced large volume change and the short diffusion length of lithium through the nano-structured sample. To further enhance the rate performance, the attempt was made to create porous tin oxide film on copper substrate by anodizing the electrodeposited tin. Nevertheless, the full anodization of tin film on a copper substrate led to the mechanical disintegration of the anodic tin oxide, due most likely to the vigorous gas evolution and the surface oxidation of copper substrate. The adhesion of anodic tin oxide to the substrate, together with the initial reversibility and cycling stability, needs to be further improved for its application to high-power electrode materials in lithium batteries.

• 한국재료학회지
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• 제20권2호
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• pp.78-81
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• 2010

Surface modification of silica nanoparticles was investigated using an aerosol self assembly. Stearic acid was used as surface treating agent. A two-fluid jet nozzle was employed to generate an aerosol of the colloidal suspension, which contained 20 nm of silica nanoparticles, surface modifier, and ethyl alcohol. Powder properties such as morphology, specific surface area and pore size distribution were analyzed by SEM, BET and BJH methods, respectively. Surface properties of the silica power were analyzed by FT-IR. The OH bond of the $SiO_2$ surface was converted to a C-H bond. It was revealed that the hydrophilic surface changed to a hydrophobic one due to the aerosol self assembly. Morphology of the surface treated powder was nanostructured with lots of pores having an average diameter of around $2\;{\mu}m$. Depending on the stearic acid concentration (0.25 to 1.0 wt%), the pore size distribution of the particles and the degree of hydrophobicity ranged from 1.5 nm to 180 nm and 29.6% to 50.2%, respectively.