• Membrane Journal
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• v.16 no.4
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• pp.286-293
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• 2006

Porous asymmetric membranes based on PVdF as a nascent membrane were prepared by using a phase inversion method. PVdF ion conductive composite membranes were finally made by introducing $SO_3{^-}$ from sulfuric acid after cross-linked PS with various DVB contents in the pores of PVdF. Final PVdF composite membranes were characterized by FTIR, SEM, EDS to verify $SO_3{^-}$. It was revealed that the solvent contents and ion exchange capacity (IEC) decreased with increase of the degree of cross-linking. As the degree of crosslink increases both the electric conductivity and methanol permeability decreased, which was showing the better values than Nafion 117. When DVB content was 8%, its electric conductivity ($5.58{\times}10^{-5}S/cm$) was similar to Nafion 117 ($6.03{\times}10^{-5}S/cm$). But the lower methanol permeability ($1.0{\times}10^{-6}cm^2/sec$) than that of Nafion 117 was obtained.

• Journal of the Korea Academia-Industrial cooperation Society
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• v.12 no.11
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• pp.5384-5391
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• 2011

The computational fluid dynamics was analyzed for the pressure distribution, stream velocity distribution, stream line field, retention time and temperature distribution which are applied to the catalyst layer in the RCO reactor to derive the optimum operating condition of the heat condensing type catalytic oxidation (RCO) reactor. The results from the computational analysis revealed that the pressure loss due to the ceramic honeycomb in the catalytic bed of the reactor which is operating currently is not significant and the stream velocity (1.8~2.7 m/s) after the ceramic filter is working in stability without big channeling. To improve the stream velocity distribution of the air stream, it is necessary to extension of the connecting range between the plenum and catalytic bed inside the facility. However, the method of attaching the air stream guide vane or the perforated plate inside the reactor was not so effective.

• Journal of the Korea Academia-Industrial cooperation Society
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• v.11 no.11
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• pp.4664-4670
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• 2010

Comparison of the classical mobile-immobile zone (MIM) model to the derived model led to several conclusions. If the MIM model is to be applied, the initial concentration in the immobile zone has to be down-scaled by a correction factor that is a function of pore geometry. The MIM model was valid only after sufficiently long time has passed, i.e., only after the diffusion front reaches the deepest pore wall in the immobile zone. The MIM mass-transfer coefficient $\alpha$, was inversely proportional to the square of the pore depth. Also it did not depend on the mobile-zone flow velocity, contrary to the number of laboratory and field observations. The classical MIM model displayed a rapid exponential decay of immobile-zone concentration. Meanwhile at large times, the newly derived model displayed similar exponential decay. This was contrary to the mounting evidence of power-law BTC tails observed in laboratory and field settings.

• Polymer(Korea)
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• v.35 no.6
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• pp.520-525
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• 2011

Superporous hydrogels (SPHs) with fast swelling and superabsorbent properties are useful materials in various biomedical fields, by improving the swelling properties of conventional hydrogels based on their unique porous structure. In this study, Eudragit polymers were used as coating materials to control the swelling properties of poly(acrylic acid-co-acrylamide) based SPHs by environmental pH. The SPHs were coated with Eudragit L100 and S100 that have different pH characteristics as enteric coating materials by a dip coating method, and their pH dependent swelling behaviors were observed in various pH environments. The swelling of SPHs was inhibited at a low pH range, but significantly enhanced above a characteristic pH of Eudragit polymers. This pH dependent swelling behavior of hydrogels could be modulated by the characteristics of the enteric coating polymers.

• Membrane Journal
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• v.29 no.3
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• pp.140-146
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• 2019

In this study, a selective layer of poly styrene sulfonic acid (PSSA) and polyethyleneimine (PEI) was formed by layer-by-layer method onto a porous polyacrylonitrile (PAN) hollow fiber membrane as the suppoter membrane. The salting out method was used by adding Mg salt to the coating solution. Several experimental conditions of the ionic strength, polymer concentration, and coating time were investigated, and the flux and rejection were measured at the operating pressure of 2 atm for 100 mg/L of NaCl, $MgCl_2$, and $CaSO_4$ as the feed solution. The membranes coated with PSSA 20,000 ppm, coating time 3 minutes, ionic strength 1.0, PEI 30,000 ppm, coating time 1 minute, and ionic strength 0.1 were observed the best. In the 100 ppm NaCl, $MgCl_2$, and $CaSO_4$ feed solutions, the flux of 20.4, 19.4, and 18.7 LMH, and the rejection of 67, 90, and 66.6%, respectively.

• Applied Chemistry for Engineering
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• v.33 no.4
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• pp.367-372
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• 2022

The effect of the addition of a polyvinylchloride (PVC) non-solvent to a PVC-tetrahydrofuran (THF) solution on the surface properties of the PVC thin film was analyzed. The non-solvents used were composed of alcohol-based and non-alcoholic ones. Surface morphologies of PVC thin films according to the addition of the non-solvent were compared. In addition, the hydrophobic properties relying on the surface characteristics were compared. The micro-bubbles generated in the preparation of PVC-THF solution affected the surface morphology of the thin film. In order to implement the normal surface physical properties of the coating thin film at the relatively high concentration of PVC-THF solution, the selection of appropriate drying method was required. When an alcohol-based non-solvent was added, a PVC thin film having a granular porous surface was obtained and exhibited super hydrophobic properties. The volume ratio of the PVC-THF solution to the non-solvent affects the surface shape of the coating thin film. The larger the amount of non-solvent was added, the more advantageous it was to form a super hydrophobic PVC thin film.

• Proceedings of the Korea Water Resources Association Conference
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• 2022.05a
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• pp.367-367
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• 2022

토지이용의 고도화에 따라 비점오염원 부하는 증가하는 추세이며 기후변화에 따른 강우강도 증가 등으로 지표면에 축적된 고농도의 비점오염물질이 하천으로 유출, 수질오염을 가중시키고 있어 비점오염원 관리가 필요하다. LID 기법은 자연적 기작(mechanisms)과 공정(process)을 이용하여 생태계의 물질순환(물순환 포함)과 에너지 흐름이 원활하도록 조성하는 기법으로, 불투수층면에서 발생되는 강우유출수를 관리 가능하다. LID 시설에는 전처리 시설을 두어 초기 고농도의 입자상 물질을 저감시키고, 강우유출수 저류공간을 통한 유출저감, 첨두유량 등을 저감시킨다. 이러한 전처리 시설에는 유기물질 및 영양소의 생물학적 제거를 위한 미생물 서식공간의 제공 등의 역할을 수행하기 위하여 다양한 여재를 적용하고 있다. 본 연구는 비점오염물질 유입이 LID 기법 전처리 시설 내 여재층의 물리·화학적 및 생물학적 환경을 평가하였다. 3개 시설 모두 100%의 불투수층에서 발생되는 강우유출수를 처리하는 LID 시설을 연구대상으로 선정하였으며, 각각의 전처리 시설에는 자갈, 우드칩, 쇄석 등이 적용되어 있다. 퇴적물의 경우 가장 상부에 존재하는 층으로 퇴적물의 오염물질 농도는 2~10.7배 이상 매우 높게 나타났다. 우드칩의 경우 다른 여재에 비해 높은 함수량과 유기물 함량을 보였으며 이는 우드칩의 수분을 보유하는 능력과 거친 표면공극에 오염물질이 부착되기 때문으로 나타났다. 또한, 같은 무기성 여재인 쇄석과 자갈의 경우 여재 크기의 차이를 보임에도 불구하고 미생물의 군집구성과 함수량의 차이를 보이는 것으로 평가되었다. 유기물의 함량이 낮은 강우유출수의 생물학적 처리능력을 향상시키기 위해서는 유기성 여재가 필요하며, 다공성 무기 멀칭재를 적용하고 하부의 토양은 적정 유기물을 배합하여 질산화 및 탈질화 유도가 가능하도록 설계가 필요한 것으로 분석되었다.

• KSCE Journal of Civil and Environmental Engineering Research
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• v.44 no.2
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• pp.183-190
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• 2024

An environmentally-friendly nanocoating method that effectively adds flame retardant(FR) and gas shielding properties to combustible polymeric construction materials such as flexible polyurethane (PU) foam was studied. Naturally-driven two-dimensional(2D) nanomaterials such as graphene oxide (GO) can exhibit liquid crystalline (LC) properties in aqueous solutions, enabling uniform coatings on the various substrates including 3D-porous foams. LC phase-assisted coating serves as 3D-scaffold, facilitating the introduction of small molecules having antioxidant capabilities such as dopamine which is to form uniformly stacked FR coating. Additionally, the structural characteristics of the 2D-materials can effectively hinder the migration of toxic gases and flammable substances in the gas phase generated during combustion. This LC phase flame retardant coating technology could be a new approach to provide environmentally friendly and effective flame retardant and gas barrier properties to various types of polymeric materials.

• Journal of the Korean Crystal Growth and Crystal Technology
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• v.34 no.5
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• pp.181-186
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• 2024

In order to solve the problems of low strength and brittle fracture of conventional concretes, ordinary cement was used as the main material of concrete binder, and porous glass beads processed from waste glass were used as aggregates to provide lightweight and fireproof insulation, and functional organic binding additives (including polymers) were added to improve concrete strength. Additional binding agents, such as silanes, were used to produce concrete-type lightweight materials with a specific gravity lower than water. The resulting materials thus manufactured have solved the problems of low work-ability and brittle fracture of conventional (ceramic) concretes, and exhibited excellent mechanical and thermal properties, with good fireproofing properties and low thermal conductivity at high temperatures. In addition, it can be molded into a certain space like conventional concrete, processed into bricks or thin boards in molds, or applied like paints, so it is believed that it can be applied to various structural materials.

• 한국신재생에너지학회:학술대회논문집
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• 2010.06a
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• pp.133.2-133.2
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• 2010

현재 융융탄산염 연료전지의 공기극으로 다공성의 lithiated NiO를 사용하고 있는데 이 재료의 경우 크게 두 가지의 문제점을 안고 있다. 첫 번째는 Ni이 전해질 내로 용해하는 것이고, 두 번째는 낮은 활성으로 인한 높은 공기극의 분극이다. Ni이 전해질로 용해되는 문제는 Co나 Fe를 코팅하여 공기극 표면에 $Li_x(Ni_yCo_{1-y})1-xO_2$나 $Li_x(Ni_yFe_{1-y})_{1-x}O_2$를 형성시켜 NiO의 전해질 내로 용해되는 것을 억제하는 방법이나 ZnO, MgO, $La_2O_3$ 등의 산화물을 NiO 표면에 코팅하여 전해질과 접촉을 막는 방식으로 해결하는 등 많은 연구가 이루어져 왔다. 하지만 연료극의 비해 상당히 높은 공기극의 분극으로 인해 큰 전압손실이 일어나 용융탄산염 연료전지 성능이 낮아지는 문제의 경우 이를 해결하고자 하는 연구는 상대적으로 많이 진행되지 못한 상태이다. 특히 현재 용융탄산염 연료전지의 장기수명화를 위해 기존의 작동온도인 $650^{\circ}C$ 보다 다소 낮은 온도인 $600{\sim}620^{\circ}C$에서 작동하려는 움직임이 있다. 작동 온도가 내려가면 전해질이 휘발되는 속도가 낮아져 전해질 부족에 따른 운전시간이 줄어드는 문제를 해결할 수 있어 장기 수명화를 위해서는 작동온도를 낮추는 것이 매우 유리하다. 하지만 작동 온도가 내려가면서 양 전극에서 일어나는 전기화학 반응 속도가 느려지기 때문에 각 전극에서의 활성화 분극으로 인한 전압손실은 더욱 커질 수밖에 없다. 특히 연료극의 수소산화반응 속도는 공기극의 산소환원반응에 비해 매우 빠르기 때문에 작동 온도가 내려감에 따라 연료극의 분극이 커지는 것에 비해 공기극의 분극이 급격히 커지게 된다. 따라서 운전온도가 낮아지는 상황에서는 낮은 작동온도에서도 성능감소가 적게 일어나 0.8V 이상 운전(150mA/$cm^2$, 단위전지 기준)이 가능한 공기극의 개발이 매우 필요한 실정이다. 이를 해결하고자 본 연구에서는 고체 산화물 연료전지의 공기극의 재료로 많이 연구되고 있는 혼합전도성 물질의 페로브스카이트 구조의 물질을 기존 NiO 전극에 코팅하여 새로운 공기극을 개발하였다. 페로브스카이트 구조의 물질로 대표적인 LSCF 물질을 사용하였으며 LSCF를 코팅한 공기극을 이용한 단위전지에서 150mA/$cm^2$의 전류를 흘려주었을 때 0.84V의 성능을 1000hr 유지하였다. 이는 기존의 NiO 전극을 사용했을 때보다 15~20mV 높은 값이다. 낮은 작동온도에서도 좋은 성능을 보였는데, 기존의 NiO 전극의 경우 $630^{\circ}C$에서 0.79V의 성능을 보인 반면 LSCF가 코팅된 공기극의 경우 $620^{\circ}C$에서 0.811V의 매우 좋은 성능을 보였다. 이는 LSCF의 산소이온전도성 및 전기전도성이 공기극에서의 분극을 낮추어 성능을 증가시키는 것으로 보인다.