In order to enhance the selective adsorption of CO₂, the surface of granular activated carbon (GAC) was modified by an ammonia solution. Ammonia in an aqueous phase could be decomposed into NH4⁺, OH^- and other N-containing elements. The present work attempted to impregnate some basic functional groups leading to chemisorption of the activated carbon surface. While the addition of N-groups reduced the specific surface area from 2071.4 m²/g to about 1300-1400 m²/g, the adsorption capacity for CO₂ increased to a certain degree, and the best amination could be achieved with the reaction at 100℃ for 12 hours. The enhanced adsorption capacity could be obtained by formation of nitrogen functionalities such as amine, pyrrolic groups and pyridine oxides which were verified by XPS analysis.

Ti-Ni alloys are widely used in numerous biomedical applications (e.g., orthodontics, cardiovascular science, orthopaedics) due to their distinctive thermomechanical and mechanical properties, such as the shape memory effect, superelasticity and low elastic modulus. In order to increase the biocompatibility of Ti-Ni alloys, many surface modification techniques, such as the sol-gel technique, plasma immersion ion implantation (PIII), laser surface melting, plasma spraying, and chemical vapor deposition, have been employed. In this study, a Ti-49.5Ni (at%) alloy was electrochemically etched in 1M H2SO4+ X (1.5, 2.0, 2.5) wt% HF electrolytes to modify the surface morphology. The morphology, element distribution, crystal structure, roughness and energy of the surface were investigated by scanning electron microscopy (SEM), energy-dispersive Xray spectrometry (EDS), X-ray diffractometry (XRD), atomic force microscopy (AFM) and contact angle analysis. Micro-sized pores were formed on the Ti-49.5Ni (at%) alloy surface by electrochemical etching with 1M H2SO4+ X (1.5, 2.0, 2.5) wt% HF. The volume fractions of the pores were increased by increasing the concentration of the HF electrolytes. Depending on the HF concentration, different pore sizes, heights, surface roughness levels, and surface energy levels were obtained. To investigate the osteoblast adhesion of the electrochemically etched Ti-49.5Ni (at%) alloy, a MTT test was performed. The degree of osteoblast adhesion was increased at a high concentration of HF-treated surface structures.

다공성 La0.6Sr0.4Ti0.3Fe0.7O3-δ로 코팅된 Ba0.5Sr0.5Co0.8Fe0.2O3-δ 관형 분리막은 압출성형 및 dip coating 방법으로 제조 되었다. 코팅된 관형 분리막의 특성은 X-선 회절분석기(XRD)와 전자 주사 현미경(SEM)을 이용하여 분석하였으며, 분석결과 2mum의 다공성 코팅 층을 갖는 페롭스카이트 구조임을 알 수 있었다. 산소투과량 분석은 750~950℃ 범위에서 공급측과 투과 측을 대기 중 공기와 진공으로 하여 수행되었다. 다공성의 La0.6Sr0.4Ti0.3Fe0.7O3-δ로 코팅된 Ba0.5Sr0.5Co0.8Fe0.2O3-δ 관형 분리막의 산소투과량은 950℃에서 3.2mL/min·cm2로 코팅되지 않은 분리막보다 높게 나타났으며, 11일 동안의 장기 안정성 실험결과 코팅 층에 의해 안정성이 증가됨을 알 수 있었다.

This present study was performed to analyze the efficiency and volatility of a porous film containing Chamaecyparis obtusa extract as a method to effectively package food compounds. Phytoncide was contacted the state of gas and showed effective antimicrobial properties. Limonene can be distilled without decomposition as a relatively stable terpene and was one of the extract components. Chamaecyparis obtusa essential oil. The optimal solvent composition was a ratio 5:20:0.3 of T-500:ethanol:hardener to effectively manufacture film containing phytoncide essential oil and the minimum antibacterial concentration was 2%. The films were made under different conditions(A-50LF1, A-25SF2, B-50SF1, C-50LF1, C-25SF2 and D-50SF1) containing phytoncide and the amounts of limonene inside the 1-L reaction chamber depending on storage were measured by gas chromatography-mass selective detention. The results showed that the 25SF2(width, 25 ㎜; length, 20 ㎝) revealed more amount of limonene compared with 50LF1(width 50 ㎜, length 20 ㎝). We confirmed that the gas emission amount showed a better layer on the film side than on the internal film. An effect of film thickness on phytoncide emissions was observed in that the amounts was less than the expectation for a thicker film at the beginning time, but the emitting amounts increased with increasing storage periods. In the storage testing of various films at 35℃ and 70% humidity for 14 days, 25SF2 showed longer preservation compared with that of 50LF in the case of bread. C. obtusa essential oil is a useful fresh ingredients, hence, analysis of limonene emission kinetics from various film was helpful to develop films with an optimal antimicrobial effect, and will allow application of such films in food packaging systems.

구조모델의 하나인 Maxwell-Eucken(ME) 모델을 이용하여 불포화 다공성 매질의 유효열전도도를 예측할 수 있는 새로운 모델을 제시하였다. 제시된 모델은 기질, 물 그리고 공기가 각각 연속상으로 존재하는 경우에 해당하는 3개 ME모델의 선형조합으로 표현되며, 매질 내에서 각 성분의 상대적 연속성 정도를 나타내는 '연속성계수'의 개념을 도입하여 선형방정식의 계수로 이용하였다. 기질의 연속성계수는 공극률과 선형의 관계를, 물과 공기의 연속성계수는 포화도와 선형 또는 비선형의 관계를 갖는 것으로 가정하였다. 공극구조가 알려진 3개 시료에 대한 열전달 모사 결과와 3개 시료의 열전도도 실험 결과를 이용하여 제시된 모델의 신뢰성을 평가하였다. 6개 시료에 대한 모델 예측값의 결정계수(R2)는 선형모델의 경우 0.86-0.98, 비선형모델의 경우 0.88-0.99로 나타나 모델의 예측 신뢰도가 매우 높은 것으로 분석되었다. 또한, 6개 시료에 대한 분석 결과를 이용하여 기질의 연속성계수와 공극률과의 관계식을 제시하였다. 따라서 본 예측모델은 기질의 열전도도, 공극률 및 포화도로부터 불포화 다공성 매질의 유효열전도도를 계산하는 데 이용될 수 있다.

In this study, gradient porous Al-Cu sintered body was fabricated by powder metallurgy processing. Al-Cu powder mixtures were prepared by low energy ball milling with various milling time. After ball milling for 3h, the shape of powder mixtures changed to spherical type with size of 100~500 . Subsequently, Al-Cu powder mixtures were classified (under 150, 150~300 and over 300 ) and compacted (20, 50 and 100 MPa). Then, they were sintered at for various holding time (10, 30, 60 and 120 min) in atmosphere. The sintered bodies had 32~45% of porosity. As a result, the optimum holding time was determined to be 60 min at and sintered bodies with various porosity were obtained by controlling the compacting pressure.

원자전달 라디칼 중합(ATRP)에 의해 poly(vinyl chloride) (PVC) 주사슬과 poly(styrene sulfonic acid) (PSSA) 곁사슬로 되어있는 양쪽성 PVC-g-PSSA 가지형 공중합체를 합성하였다. PVC-g-PSSA 가지형 공중합체 고분자를 템플레이트로 사용하고 졸겔법을 적용하여, 결정성 아타네제상의 미세기공 이산화티타튬 필름을 제조하였다. TiO2 전구체인 TTIP를 친수성인 PSSA 영역과 선택적으로 작용시켜 TiO2 메조기공 필름을 성장하였으며, 이를 주사전자 현미경 (SEM)과 엑스레이회절 (XRD)분석을 통해 분석하였다. 스핀코팅 횟수와 P25 도입에 따른 염료감응 태양전지 성능을 체계적으로 분석하였다. 그 결과 준고체 고분자 전해질을 이용하였을 때, 100 mW/㎠ 조건에서 에너지 변환 효율이 2.7%에 이르렀다.

The synthesis behavior of nanoporous silica aerogel in the macroporous ceramic structure was observed using TEOS as a source material and glycerol as a dry control chemical additive (DCCA). Silica aerogel in the macroporous ceramic structure was synthesized via sono-gel process using hexamethyldiazane (HMDS) as a modification agent and n-hexane as a main solvent. The wet gel with a modified surface was dried at under ambient pressure. The addition of glycerol appears to give the wet gel a more homogeneous microstructure. However, glycerol also retarded the rate of surface modification and solvent exchange. Silica aerogel completely filled the macroporous ceramic structure without defect in the condition of surface modification (20% HMDS/nhexane at 36hr).

The RFID (Radio-Frequency Identification) is an automatic identification method, relying on storing and remotely retrieving data using devices called RFID tags or transponders. Some RFID tags have been used in severe environment of temperature ranged from to for a long time and may cause serious problems such as signal error, short life cycle and explosion. Conventionally, the RFID tags for high temperature applications consisted of Fe-alloy housing part, ceramic powder and RFID sensor. However, it has disadvantage of heavy weight, signal noise and heat shield capability. In this study, we newly applied the aluminum porous materials fabricated by polymer leaching process into RFID tags in order to improve heat shielding ability, and compared the properties of RFID tag inserted by aluminum porous with the conventional one.

본 연구에서는 다공성 polyethylene (PE) 이차전지용 격리막에 poly(ethylenimine) (PEI)을 함침시켜 isophthaloyl dichloride (IPC)을 이용한 가교반응 통하여 음이온교환막을 제조하였다. 제조된 막의 특성화를 평가하기 위하여 함수율, 접촉각, FT-IR, 이온교환용량, 이온전도도 등을 측정하였다. PEI와 IPC의 반응은 아민과 -COCl기와의 반응으로 아마이드기가 생성된다. 이온교환용량의 경우 30초 반응에서 1.96 meq./g dry membrane부터 600초 반응으로 인한 1.14 meq./g dry membrane까지 감소하는 경향을 나타내었고, 이온전도도의 경우 IPC와의 가교시간이 30초일 때 9.15×10-2S/㎝의 높은 값을 나타냄을 확인할 수 있었다.

에멀션 기반의 계면활성제를 이용한 주형합성법을 이용하여 산촉매로서 염산과 실리카의 전구체인 테 트라에톡시실란을 사용함으로써 메조다공성 실리카 마이크로스피어를 합성하였다. 테트라에톡시실란의 농도 증가에 의해 구형의 입자 형태가 파괴되었고, 기공구조도 크게 변하였다. 산촉매 농도 증가에 의한 구형의 입자형태 파괴 현상은 적었지만 상대적으로 작은 크기의 구형의 마이크로입자가 더 많이 생성되 었다. 하지만, 산성조건에서 입자들 간의 강한 응집현상이 나타남에 따라 낱개의 분리되어 있는 단일입자 를 얻기 위해서는 초음파 등의 후처리 과정이 필요하였다.

As a pore precursor, carbon black with different content of 0 to 60 vol% were added to (Ba,Sr) powder. Porous (Ba,Sr) ceramics were prepared by pressureless sintering at for 1h under air. Effects of carbon black content on the microstructure and PTCR characteristics of porous (Ba,Sr) ceramics were investigated. The porosity of porous (Ba,Sr) ceramics increased from 6.97% to 18.22% and the grain size slightly decreased from to with increasing carbon black contents. PTCR jump of the (Ba,Sr) ceramics prepared by adding carbon black was more than , and slightly increased with increasing carbon black. The PTCR jump in the (Ba,Sr) ceramics prepared by adding 40 vol% carbon black showed an excellent value of , which was above two times higher than that in (Ba,Sr) ceramics. These results correspond with Heywang model for the explanation of PTCR effect in (Ba,Sr) ceramics. It was considered that carbon black is an effective additive for preparing porous based ceramics. It is believed that newly prepared (Ba,Sr) cermics can be used for PTC thermistor.

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.

A porous nickel-tin nano-dendritic electrode, for use as the anode in a rechargeable lithium battery, has been prepared by using an electrochemical deposition process. The adjustment of the complexing agent content in the deposition bath enabled the nickel-tin alloys to have specific stoichiometries while the amount of acid, as a dynamic template for micro-porous structure, was limited to a certain amount to prevent its undesirable side reaction with the complexing agent. The ratios of nickel to tin in the electro-deposits were nearly identical to the ratios of nickel ion to tin ion in the deposition bath; the particle changed from spherical to dendritic shape according to the tin content in the deposits. The nickel to tin ratio and the dendritic structure were quite uniform throughout the thickness of the deposits. The resulting nickel-tin alloy was reversibly lithiated and delithiated as an anode in rechargeable lithium battery. Furthermore, the resulting anode showed much more stable cycling performance up to 50 cycles, as compared to that resulting from dense electro-deposit with the same atomic composition and from tin electrodeposit with a similar porous structure. From the results, it is expected that highly-porous nickel-tin alloys presented in this work could provide a promising option for the high performance anode materials for rechargeable lithium batteries.