본 연구에서는 다양한 실내시험을 통하여 국내에서 개발된 에폭시 아스팔트 혼합물의 공용성을 평가하였다. 최대입경 13mm의 밀입도 혼합물을 기초로 하여 아스팔트 바인더의 20% 또는 40%를 국산 및 일본산 에폭시 수지로 치환하여 4종류의 에폭시 아스팔트 혼합물의 배합 설계를 실시하였다. 에폭시 아스팔트의 가사시간이 에폭시 수지가 40% 사용한 경우 3시간, 20% 사용한 경우 6시간 정도임을 확인할 수 있었다. 휠트랙킹 시험, 간접인장 반복시험, 그리고 저온 휨 시험 결과 국산 및 일본산 에폭시 아스팔트 혼합물의 공용성이 일반 아스팔트 혼합물 보다 상당히 우수한 것으로 나타났다. 하지만 일부 에폭시 아스팔트 혼합물에서는 수분손상 가능성을 확인할 수 있었다. 또한 일본산 에폭시 아스팔트 혼합물과 국산 에폭시 아스팔트는 유사한 성능을 나타냈다. 또한 콘크리트 보수재로 개발한 국산 에폭시 아스팔트의 적합성을 평가하기 위하여 추가적으로 열팽창계수, 부착강도, 인장강도를 측정한 결과, 일반 콘크리트와의 부착력은 우수하고 인장강도는 유사한 것으로 나타났으나 열팽창계수는 5배정도 큰 것으로 나타났다.

Silicon-based thin film was prepared at room temperature by an electrochemical deposition method and a feasibility study was conducted for its use as an anode material in a rechargeable lithium battery. The growth of the electrodeposits was mainly concentrated on the surface defects of the Cu substrate while that growth was trivial on the defect-free surface region. Intentional formation of random defects on the substrate by chemical etching led to uniform formation of deposits throughout the surface. The morphology of the electrodeposits reflected first the roughened surface of the substrate, but it became flattened as the deposition time increased, due primarily to the concentration of reduction current on the convex region of the deposits. The electrodeposits proved to be amorphous and to contain chlorine and carbon, together with silicon, indicating that the electrolyte is captured in the deposits during the fabrication process. The silicon in the deposits readily reacted with lithium, but thick deposits resulted in significant reaction overvoltage. The charge efficiency of oxidation (lithiation) to reduction (delithiation) was higher in the relatively thick deposit. This abnormal behavior needs to clarified in view of the thickness dependence of the internal residual stress and the relaxation tendency of the reaction-induced stress due to the porous structure of the deposits and the deposit components other than silicon.

Thin film electrode consisting purely of porous anodic tin oxide with well-defined nano-channeled structure was fabricated for the first time and its electrochemical properties were investigated for application to an anode in a rechargeable lithium battery. To prepare the thin film electrode, first, a bi-layer of porous anodic tin oxides with well-defined nano-channels and discrete nano-channels with lots of lateral micro-cracks was prepared by pulsed and continuous anodization processes, respectively. Subsequent to the Cu coating on the layer, well-defined nano-channeled tin oxide was mechanically separated from the specimen, leading to an electrode comprised of porous tin oxide and a Cu current collector. The porous tin oxide nearly maintained its initial nano-structured character in spite of there being a series of fabrication steps. The resulting tin oxide film electrode reacted reversibly with lithium as an anode in a rechargeable lithium battery. Moreover, the tin oxide showed far more enhanced cycling stability than that of powders obtained from anodic tin oxides, strongly indicating that this thin film electrode is mechanically more stable against cycling-induced internal stress. In spite of the enhanced cycling stability, however, the reduction in the initial irreversible capacity and additional improvement of cycling stability are still needed to allow for practical use.

본 연구에서는 용액 캐스팅법을 이용하여 각기 다른 함량의 VMT가 첨가된 SPAES/VMT 복합막이 제조되었다. SPAES 매트릭스 내의 VMT입자 분산은 전자주사현미경으로 관찰된 평균분포에 의해 확인되었다. 1 wt%보다 적은 함량을 포함한 복합막은 고분자 매트릭스 내에 좋은 분산성을 나타내어 막의 상부층과 하부층에 매끈한 표면을 가졌다. 복합막의 함수율은 온도가 증가함에 따라 급격하게 증가되었으며 VMT는 높은 이온교환능력으로 인하여 강한 수분친화도를 가짐으로 인해 높은 모든 흡착된 수분은 bound water인 것으로 확인하였다. VMT의 함량이 1 wt%보다 적게 첨가된 복합막에서 증가된 이온전도도와 낮아진 메탄올 투과도를 확인할 수 있었다. 모든 복합막 중에서 SPAES/VMT 1.0 wt% 복합막은 선택도 측면에서 가장 뛰어난 연료전지 성능을 가졌으며 Nafion 112과 비교하여 두배 이상 우수한 값을 나타내었다. 이것은 SPAES/VMT 1.0 wt% 복합막이 직접메탄올 연료전지의 구동을 위한 가장 우수한 조건이 될것이라 사료된다.

일반적으로 도로 포장체의 파손은 다양한 요소에 영향을 받는 것으로 알려져 있다. 그 중 가장 주된 포장체 파손형태로서 영구변형(permanent deformation)과 피로균열(fatigue crack)을 들 수 있으며 이들은 포장체의 공용수명을 단축시키는 주요원인이 된다. 도로 포장체의 영구변형을 정확히 예측하는 것은 도로포장체의 내구성을 파악하여 이를 기반으로 포장을 설계하는 포장설계법의 수립에 있어 매우 중요하다. 포장하부구조의 재료거동은 본질적으로 전단강도(τmax)와 밀접한 연관성을 가지므로 포장하부구조 내 발생한 전단응력τ의 전단강도에 대한 발생비를 고려하여 영구변형 모델을 설정할 필요가 대두되고 있다. 이에 본 연구에서는 이와 같은 전단응력비 개념을 도입한 대형반복삼축압축시험을 통하여 도로하부 재료 중 국내에서 사용되는 대표적인 입상의 보조기층 재료에 대한 영구변형 특성을 알아보았으며 이를 기초로 영구변형 모델의 수립에 필요한 모델 매개변수를 시험을 통해 새롭게 제안하고자 하였다.

단립종 100%, 장립종 100%, 단립종 50%와 팽화미분 50% 그리고 장립종 50%와 팽화미분 50%로 제조한 탁주의 pH, 산도, 단백질, 색도, 환원당, 총당, 알코올 그리고 관능성질을 조사하였다. 모든 시료의 pH는 발효 초기에 급격히 감소한 후 장립종 100%를 제외하고 서서히 상승하였다. 발효 2일 후 단립종은 장립종보다 그리고 팽화미분은 순 쌀보다 같거나 높았다(p < 0.05). 산도는 발효 시간 지낼수록 모든 시료에서 증가하였다. 장립종 100%는 단립종 100%보다 3일부터 그리고 장립종 50%는 단립종 50%보다 4일부터 높았다(p < 0.05). 모든 시료의 단백질은 1일에 증가한 후 감소하였고 팽화미분은 순 쌀과 같거나 높았다(p < 0.05). L값은 모든 시료에서 발효 초기에 증가한 후 감소하였다. 발효 4일부터 단립종은 장립종보다 그리고 3일부터 팽화미분은 순 쌀보다 L값이 낮았다. 담금 직후부터 순 쌀의 a값은 점점 감소하였고 팽화미분은 3일 때까지 증가하다가 감소하였다. 모든 시료의 b값은 발효 2와 3일에 최고값을 보인 후(p < 0.05) 감소하는 경향을 보였다. 담금 직후 팽화미분은 순 쌀보다 환원당이 훨씬 높았다. 순 쌀은 발효 1일에 증가한 후 감소하였고 팽화미분은 급격히 감소하였다. 총당은 환원당과 유사하였다. 알코올은 발효 2일까지 모든 시료에서 급격히 증가하였고 단립종은 장립종보다 그리고 팽화미분은 순 쌀보다 항상 높았다(p < 0.05). 단립종 100%와 장립종 100%는 1% 수준에서 유의적인 차이가 있었지만 선호도는 차이가 없었다. 단립종 50%와 장립종 50%는 유의적으로 차이가 없었다.

Yttrium oxide is one of the most thermo-dynamically stable materials, so that it is generally used as a dispersoid in many kinds of dispersion strengthed alloys. In this study, a nickel-base superalloy is strengthened by dispersion of yttrium oxide particles. Elemental powders with the composition of Ni-22Cr-18Fe-9Mo were mechanically alloyed(M.A.) with 0.6 wt% . The MA powders were then HIP(hot isotactic press)ed and hot rolled. Most oxide particles in Ni-22Cr-18Fe-9Mo base ODS alloy were found to be Y-Ti-O type. The oxide particles were uniformly dispersed in the matrix and also on the grain boundaries. Tensile test results show that the yield strength and ultimate tensile strength of ODS alloy specimens were 1.2~1.7 times higher than those of the conventional X(R), which has the same chemical compositions with ODS alloy specimens except the oxide particles.

In this study, p-type : TAGS-85 compound powders were prepared by gas atomization process, and then their microstructures and mechanical properties were investigated. The fabricated powders were of spherical shape, had clean surface, and illustrated fine microstructure and homogeneous + GeTe solid solution. Powder X-ray diffraction results revealed that the crystal structure of the TAGS-85 sample was single rhombohedral GeTe phase, which with a space group . The grain size of the powder particles increased while the micro Vickers hardness decreased with increasing annealing temperature within the range of 573 K and 723 K due to grain growth and loss of Te. In addition, the crystal structure of the powder went through a phase transformation from rhombohedral () at low-temperature to cubic () at high-temperature with increasing annealing temperature. The micro Vickers hardness of the as-atomized powder was around 165 Hv, while it decreased gradually to 130 Hv after annealing at 673K, which is still higher than most other fabrication processes.

기질 고분자인 sulfonated PEEK (sPEEK)와 가교제(cross-linking reagent) 4,4'-ethyldianiline (EdAn), 그래프트제(grafting reagent) 2-phenylethylamine (PEA)을 용매 dimethylacetamide (DMAc)에 녹여 용매증발법을 이용하여 제막하였다. 이민화 반응(imination)과 술폰화(sulfonation) 과정을 거쳐 최종 이온교환막인 cross-linked and grafted sPEEK (CG-sPEEK)막을 제조하였다. FT-IR 분석을 통해 술폰화 및 이민화 반응여부를 확인할 수 있었다. Proton conductivity와 water uptake, volume change를 측정하여 상용화된 Nafion115와 비교함으로써 이온교환막으로서의 활용가능성을 평가하였다. 제조된 CG-sPEEK막의 proton conductivity (0.17 S/cm) 값이 Nafion115 (0.10 S/cm) 보다 우수하게 나타나 이온교환막으로서의 적용가능성을 보여주었다. 다만 높은 water uptake (130%)는 CG-sPEEK의 치수안정성을 위해서 저감시킬 필요가 있다.

Odors were produced in the reactor where contained the swine excreta sampled from the pigery and were analyzed the major odor materials based on the odor contribution index. The container hoggery where six pens were separated was set up in S-myun, Gyeonggi-do, Korea: one was control group, the other were experimental group. Sixty weaners were raised and their excreta were sampled every week to the test of the effect of feed type probiotics. Some probiotics showed very effective deodorizing activity during the whole experimental periods. All products had positive effects on the reducing odor intensities after 4 to 5 week periods. The odor contribution analysis represented the main odor compounds were trimethylamine and volatile sulfur compounds such as hydrogen sulfide, mercaptane, and dimethyl sulfide.

Nano-sized Y2O3 powders were prepared via a sol-gel method starting with Y(NO3)3·6H2O (Yttrium(III) nitrate hexahydrate) and water with ethanol as a cosolvent. Y2O3 is an important rare earth oxide and has been considered for use in nuclear applications, such as ceramic materials, due to its excellent optical and refractory characteristics. It has been used as a chemically stable substrate, a crucible material for melting reactive metals, and a nozzle material for jet casting molten rare earth-iron magnetic alloys. Oxalic acid (C2H2O4) has been adopted as a chelating agent in order to control the rate of hydrolysis and polycondensation, and ammonia was added in order to adjust the base condition. The synthesized Y2O3 powder was characterized using TG/DTA, XRD, FE-SEM, BET and Impedance Analyzer analyses. The powder changed its properties in accordance with the pH conditions of the catalyst. As the pH increases according to the FE-SEM, the grain grew and it showed that the pore size decreased while confirming the effect of the grain size. The nano-material Y2O3 powders demonstrated that the surface area was improved with the addition of oxalic acid with ammonium hydroxide.

The industrial manufacturing of YSZ products can be summarized as a three step process: a) hydrolysis of zirconyl chloride and mixing of other solutions, b) precipitation, and c) calcination. The addition of ammonia or OH- is essential in the precipitation process. However, a strong agglomeration was observed in the results of an ammonia or OH- addition. Thus, it is necessary to disperse the powders smoothly in order to improve the mechanical strength of YSZ. In this study, YSZ was synthesized using the urea stabilizer and hydrothermal method. YSZ powders were synthesized using a hydrothermal method with Teflon Vessels at 180˚C for 24 h. The mole ratio of urea to Zr was 0, 0.5, 1, and 2. The crystal phase, particle size, and morphologies were analyzed. Rectangular specimens (33 mm×8 mm×1±0.5 mm) for three-point bend tests were used in the mechanical properties evaluation. The crystalline of YSZ powders observed a tetragonal phase in the sample with a ratio of Zr:urea = 1:2 addition and a hydrothermal reaction time of 24 h. The average primary particle size of YSZ was measured to be 9 nm to 11 nm. The agglomerated particle size was measured from 15 nm to 30 nm. The three-point bending strength of the YSZ samples was 142.47 MPa, which is the highest value obtained for the Zr:urea = 1:2 ratio addition YSZ sample.

This study deals with the high frequency induction hardening (HF at 850℃, 120kHz & 50kW condition) SM45C steel. (1) The HF specimen, which was tempered at 150℃, did not show any tempering effect. A brittle fracture occurred at rounded area of the tensile specimen. AE (acoustic emission) amplitude distribution showed between 45dB and 60dB. (2) A slip and fracture occurred at the hole area of the HF specimen which was tempered at 300℃. As they pass the yield point, the AE energy is increased intermittently and AE amplitude distribution exists between 70dB and 85dB. In addition, after imposing the maximum tensile load, AE signals showed high amplitude and energy distribution. The AE amplitude showed between 45dB and 70dB. (3) A brittle fracture occurred at HF specimen which was tempered at 450℃ as if it is torn in the direction of 45° on parallel area over the both sides of the tensile specimen, which lead to several peak appeared in AE energy. It was found that the AE amplitude was relatively low and the AE energy was high.

본 연구의 목적은 중온화 첨가제(LEADCAP®)를 사용한 중온 아스팔트 바인더의 노화 방법에 따른 물성 변화 특성을 평가하고자 하였다. 아스팔트 바인더의 노화 거동을 모사하기 위해 단기노화인 RFTO를 실시하였으며, 햇빛에 의한 자연 노화 거동을 알아보기 위해 자외선 경화기를 이용하여 자외선에 의한 열화거동을 모사하였다. 이러한 열화 중온 아스팔트 바인더의 역학적인 물성과 유변동학적인 특성을 시험하기 위해서 만능시험기(UTM)과 동적전단유동기를 이용하여 직접인장력과 유변동학적인 거동을 평가하였다. 또한, 열분석 장비를 이용하여 온도에 따른 중온 아스팔트 바인더의 특성을 평가하여, 자외선 노출에 따른 열화가 발생하여도 온도에 따른 물성 변화가 많이 발생하지 않음을 발견하였다. 70℃에서 중온화 첨가제가 첨가한 단기노화 중온 아스팔트 바인더의 경우, PG 등급에서의 고온 등급의 기준값을 만족함을 알 수 있었다. 또한 저온에서 중온 아스팔트 바인더의 인장 특성을 평가한 결과, 인장강도 향상과 함께 인장력이 증가됨을 알 수 있었다.

Negative temperature coefficient (NTC) materials have been widely studied for industrial applications, such assensors and temperature compensation devices. NTC thermistor thick films of Ni1+xMn2-xO4+δ (x=0.05, 0, −0.05) werefabricated on a glass substrate using the aerosol deposition method at room temperature. Resistance verse temperature (R-T)characteristics of the as-deposited films showed that the B constant ranged from 3900 to 4200 K between 25oC and 85oCwithout heat treatment. When the film was annealed at 600oC 1h, the resistivity of the film gradually decreased due tocrystallization and grain growth. The resistivity and the activation energy of films annealed at 600oC for 1 h were 5.203, 5.95,and 4.772KΩ·cm and 351, 326, and 299meV for Ni0.95Mn2.05O4+δ, NiMn2O4, and Ni1.05Mn1.95O4+δ, respectively. The annealingprocess induced insulating Mn2O3 in the Ni deficient Ni0.95Mn2.05O4+δ composition resulting in large resistivity and activationenergy. Meanwhile, excess Ni in Ni1.05Mn1.95O4+δ suppressed the abnormal grain growth and changed Mn3+ to Mn4+, givinglower resistivity and activation energy.

The present study was carried out to evaluate the microstructural and mechanical properties of cross-roll rolled pure copper sheets, and the results were compared with those obtained for conventionally rolled sheets. For this work, pure copper (99.99 mass%) sheets with thickness of 5 mm were prepared as the starting material. The sheets were cold rolled to 90% thickness reduction and subsequently annealed at 400˚C for 30 min. Also, to analyze the grain boundary character distributions (GBCDs) on the materials, the electron back-scattered diffraction (EBSD) technique was introduced. The resulting cold-rolled and annealed sheets had considerably finer grains than the initial sheets with an average size of 100 μM. In particular, the average grain size became smaller by cross-roll rolling (6.5 μM) than by conventional rolling (9.8 μM). These grain refinements directly led to enhanced mechanical properties such as Vickers micro-hardness and tensile strength, and thus the values showed greater increases upon cross-roll rolling process than after conventional rolling. Furthermore, the texture development of<112>//ND in the cross-roll rolling processed material provided greater enhancement of mechanical properties relative to the case of the conventional rolling processed material. In the present study, we systematically discuss the enhancement of mechanical properties in terms of grain refinement and texture distribution developed by the different rolling processes.

The electro-deposition of compound semiconductors has been attracting more attention because of its ability torapidly deposit nanostructured materials and thin films with controlled morphology, dimensions, and crystallinity in a cost-effective manner (1). In particular, low band-gap A2B3-type chalcogenides, such as Sb2Te3 and Bi2Te3, have been extensivelystudied because of their potential applications in thermoelectric power generator and cooler and phase change memory.Thermoelectric SbxTey films were potentiostatically electrodeposited in aqueous nitric acid electrolyte solutions containingdifferent ratios of TeO2 to Sb2O3. The stoichiometric SbxTey films were obtained at an applied voltage of −0.15V vs. SCE usinga solution consisting of 2.4mM TeO2, 0.8mM Sb2O3, 33mM tartaric acid, and 1M HNO3. The stoichiometric SbxTey filmshad the rhombohedral structure with a preferred orientation along the [015] direction. The films featured hole concentrationand mobility of 5.8×1018/cm3 and 54.8cm2/V·s, respectively. More negative applied potential yielded more Sb content in thedeposited SbxTey films. In addition, the hole concentration and mobility decreased with more negative deposition potential andfinally showed insulating property, possibly due to more defect formation. The Seebeck coefficient of as-deposited Sb2Te3 thinfilm deposited at −0.15V vs. SCE at room temperature was approximately 118µV/K at room temperature, which is similarto bulk counterparts.

In case of general concrete, autogenous shrinkage is about 10% of the drying shrinkage. Therefore it was not considered significant to be a subject matter about managing the crack control and design. It was reported that cracks can be generated from the autogenous shrinkage. Because of the low W/B rate and the high unit binder of the high strength concrete. In this study, autogenous shrinkage and drying shrinkage are examined which is the main reason of the cracks of the high strength concrete based on the previous studies. Comparing the data from this study and previous studies, we developed the shrinkage reduced concrete using shrinkage reducing agent. The purpose of this study is to provide the data for reducing and managing the column shortening of the high strength concrete structures.