Red-emitting Eu3+-activated (Y0.95-xAlx)VO4 (0<x≤0.12) nanophosphors with the particle size of ~30nm and thehigh crystallinity have been successfully synthesized by a hydrothermal reaction. In the synthetic process, deionized water asa solvent and ethylene glycol as a capping agent were used. The crystalline phase, particle morphology, and thephotoluminescence properties of the excitation spectrum, emission intensity, color coordinates and decay time, of the prepared(Y0.95-xAlx)VO4:Eu3+ nanophosphors were compared with those of the YVO4:Eu3+. Under 147nm excitation, (Y0.95-xAlx)VO4nanophosphors showed strong red luminescence due to the 5D0-7F2 transition of Eu3+ at 619nm. The luminescence intensityof YVO4:Eu3+ enhanced with partial substitution of Al3+ for Y3+ and the maximum emission intensity was accomplished at theAl3+ content of 10mol%. By the addition of Al3+, decay time of the (Y,Al)VO4:Eu3+ nanophosphor was decreased in comparisonwith that of the YVO4:Eu3+ nanophosphor. Also, the substitution of Al3+ for Y3+ invited the improvement of color coordinatesdue to the increase of R/O ratio in emission intensity. For the formation of transparent layer, the red nanophosphors werefabricated to the paste with ethyl celluloses, anhydrous terpineol, ethanol and deionized water. By screen printing method, atransparent red phosphor layer was formed onto a glass substrate from the paste. The transparent red phosphor layer exhibitedthe red emission at 619nm under 147nm excitation and the transmittance of ~80% at 600nm.

In this study, Platinum(Pt) nanoparticles were synthesized by using polyol process which is one of the liquid phase reduction methods. Dihydrogen hexachloroplatinate (IV) hexahydrate , as a precursor, was dissolved in ethylene glycol and silver nitrate () was added as metal salt for shape control of Pt particle. Also, polyvinylpyrrolidone (PVP), as capping agent, was added to reduce the size of particle and to separate the particles. The size of Pt nanoparticles was evaluated particle size analyzer (PSA). The size and morphology of Pt nanoparticles were observed by transmission electron microscopy (TEM) and high resolution TEM (HRTEM). Synthesized Pt nanoparticles were studied with varying time and temperature of polyol process. Pt nanoparticles have been successfully synthesized with controlled sizes in the range 5-10 and 20-40 nm with cube and multiple-cube shapes.

이 연구에서는 추계학적 그린함수법에 의한 단층 모델을 이용하여 지진파를 합성하고 단층 파라미터의 변화에 의한 지반 운동의 차이를 평가하였다. 모멘트 규모 6.5의 단층을 예제로 선정하였고 아스페리티 면적의 통계값을 이용하여 슬립의 분포를 모델링하였다. 평가를 위해 고려된 단층 파라미터들은 진원의 위치, 전단파 속도 대비 파열 전파속도 비, 상승시간, 절점주파수 그리고 고주파감쇠 필터 등 이었다. 요소지진원에 적용된 파라미터들은 구조권역별 특성이 다른 지역의 값을 사용하였고 다른 파라미터들은 발생 가능한 임의의 값을 사용하였다. 생성된 지반운동 시간이력으로부터 응답스펙트럼을 작성하였으며, 파라미터의 값을 달리하여 비교하였다.이로부터 각각의 단층파라미터에 의해 영향을 받는 주파수 구간 및 스펙트럼 가속도의 차이를 평가하였다.

Electricity is generated by the combined reactions of hydrogen oxidation and oxygen reduction which occur on the Pt/C catalyst surface. There have been lots of researches to make high performance catalysts which can reduce Pt utilization. However, most of catalysts are synthesized by wet-processes and a significant amount of chemicals are emitted during Pt/C synthesis. In this study, Pt/C catalyst was produced by arc plasma deposition process in which Pt nano-particles are directly deposited on carbon black surfaces. During the process, islands of Pt nano-particles were produced and they were very fine and well-distributed on carbon black surface. Compared with a commercialized Pt/C catalyst (Johnson & Matthey), finer particle size, narrower size distribution, and uniform distribution of APD Pt/C resulted in higher electrochemical active surface area even at the less Pt content.

양극산화 알루미나(AAO)막의 나노 사이즈 미세공(세공 크기 20 nm, 10 nm 및 200 nm)을 주형으로 사용하여 전도성 고분자인 폴리피롤, 폴리아닐린 중합체 및 폴리피롤/폴리아닐린 공중합체 나노와이어를 제조하였다. 미세공 주형 내에서 전도성 고분자의 성장은 세공의 벽면을 따라 튜브 형태로서 성장하였으며, 3시간 이후에는 내부가 완전히 채워진 나노와이어가 형성되었다. AAO 막을 수산화나트륨 용액으로 퍼리하여 세공 내에 형성된 전도성 고분자 나노와이어를 회수 하였으며. 회수된 나노와이어 직경과 길이는 주형 막의 세공 형상과 일치하였다. 통상의 용액 중합법으로 제조된 전도성 고분자 분말과 비교하여 주형 합성법으로 제조된 전도성 고분자 나노와이어는 결정성과 열적 안정성이 향상되었으며, 전기 저항은 4~60% 감소하였다.

1-D ZnO nanowires have been attractive for their peculiar properties and easy growth at relatively low temperature. The length, diameter, and density of ZnO nanowires were determined by the several synthetic parameters, such as PEI concentration, growth time, temperature, and zinc salt concentration. The ZnO nanowires were grown on the<001> oriented seed layer using the hydrothermal process with zinc nitrate and HMTA (hexamethylenetetramine) and their structure and optical properties were characterized. The morphology, length and diameter of the nanowires were strongly affected by the relative and/or absolute concentration of Zn2+ and OH-1 and the hydrothermal temperature. When the concentrations of the zinc nitrate HMTA were the same as 0.015 M, the length and diameter of the nanowires were 1.97μm and 0.07μm, respectively, and the aspect ratio was 28.1 with the preferred orientation along the<001> direction. XRD and TEM results showed a high crystallinity of the ZnO nanowires. Optical measurement revealed that ZnO nanowires emitted intensive stimulated UV at 376 nm without showing visible emission related to oxygen defects.

A3-2x/3Al1-zInzO4F: Eux3+ (A=Ca, Sr, Ba, x=-0.15, z=0, 0.1) oxyfluoride phosphors were simply prepared by thesolid-state method at 1050oC in air. The phosphors had the bright red photoluminescence (PL) spectra of an A3-2x/3Al1-zInzO4Ffor Eu3+ activator. X-ray diffraction (XRD) patterns of the obtained red phosphors were exhibited for indexing peak positionsand calculating unit-cell parameters. Dynamic excitation and emission spectra of Eu3+ activated red oxyfluoride phosphors wereclearly monitored. Red and blue shifts gradually occurred in the emission spectra of Eu3+ activated A3AlO4F oxyfluoridephosphors when Sr2+ by Ca2+ and Ba2+ ions were substituted, respectively. The concentration quenching as a function of Eu3+contents in A3-2x/3AlO4F:Eu3+ (A=Ca, Sr, Ba) was measured. The interesting behaviors of defect-induced A3-2x/3Al1-zInzO4-αF1-δphosphors with Eu3+ activator are discussed based on PL spectra and CIE coordinates. Substituting In3+ into the Al3+ positionin the A3-2x/3AlO4F:Eu3+ oxyfluorides resulted in the relative intensity of the red emitted phosphors noticeably increasing byseven times.

It is known that the content of saturated fatty acids methyl ester (SFAME) affect the pour point of biodiesel at low temperature. In this study, biodiesel (BD) was produced from beef tallow (TAL) by alkali catalyst. To reduce the saturation in BD, acetone fractionation was applied. Besides, TAL was also solvent-fractionated to reduce the saturated fatty acid (SFA) content for further producing BD. With acetone, TAL or TAL methyl ester (5:1 v/w) were fractionated at 10, 0, -10, and -15℃, respectively. At -10℃, 17.35% of SFA was observed in fractionated TAL (liquid part, -10TAL) when 5:1 solvent ratio was used for 24 hr. Under the same condition, fractionated BD (liquid part, -10BD) showed SFA (33.14%) with 78wt % yield. Also, fractionation of BD with different concentration of crystallizer 209 (0.1, 0.5, and 1%) along with different time (2, 6, 12, and 24 hr.) was observed. The best condition for reducing the SFA was 0.5% of crystallizer 209 addition for 12 hr of fractionation time at -10℃, in which 30.14% of SFA content was observed in BD (liquid part). Among different crystallizer, ps 66 showed the least content of SFA content (23.28%) in BD after fractionation (-10℃ and 24 hr) with 0.5wt% addition.

Chitosan is widely used in cosmetics and medical fields. Special emphasis has been put on the chemical modification of chitosan to explore its full potential. We have described the synthesis and biological activity of novel peptide amino acid derivatives. The polyamino acid derivatives were synthesized by introducing alkylamine functional group on chitosan at C-6. The poor aqueous solubility of chitosan derivatives hinder both pharmacological studies and pharmaceutical development. To make amino acid coupled chitosan derivatives with improved biological effect and solubility, some attempts have been taken to consist of amino peptide group like aspartic acid and phenylalanine-aspartic acid derivatives onto chitosan C-6. The resultingly substituted chitosan was characterized by solubility in various solvents. We measured chitosan derivatives with 1H-NMR and 13C-NMR. Also, We were investigated on the physical properties and biological activities of these products.

이 연구는 새로운 형태의 FRP-콘크리트 합성말뚝인 하이브리드 CFFT(HCFFT)를 개발하는 과정의 일부이다. 이 논 문에서는 CFFT와 HCFFT의 압축강도실험을 통하여 구조적 거동을 분석하였다. 압축강도실험에 앞서 PFRP와 FFRP 재료의 역학적 성질을 조사하였다. HCFFT 압축강도실험은 콘크리트 강도와 FFRP의 두께를 변수로 하여 실험을 수 행하였다. 그리고, FFRP 두께를 변수로 PFRP를 제외한 CFFT 실험체를 제작하고 실험을 수행하여 HCFFT와 비교· 분석하였다. 실험 결과, HCFFT의 압축강도는 CFFT에 비하여 11~47% 향상되는 것으로 나타났다. 실험구간내의 필 라멘트 와인딩 FRP 보강두께의 증가에 따른 HCFFT의 압축강도는 선형으로 증가시키는 것으로 나타났다. 또한 실 험체와 동일한 조건의 유한요소해석을 수행하였다. 해석결과는 실험결과에 비하여 모든 시편에서 약간 작은 값을 보였으며, 0.14%에서 17.95%까지의 오차범위 내에 있음을 알 수 있었다.

본 논문에서는 컴퓨터 시뮬레이션을 통해 강재-FRP 합성 교량용 방호울타리의 성능을 분석하였다. FRP는 Surface veil, DB 그리고 Roving 섬유로 구성하였다. FRP의 적층을 고려하기 위해 LS-DYNA에서 제공하는 재료모델 MAT58을 사용하였다. 강관과 FRP의 접촉조건을 고려하기 위해 Spot weld 옵션을 사용하였다. 실차충돌 실무 업무편람에 따 라 구조적 강도성능, 탑승자 보호성능 및 충돌 후 차량의 거동에 대한 성능평가를 실시하였다. 강재-FRP 합성 방호 울타리는 성능평가를 만족하였다.

본 연구는 각 연결부에 대한 수치 해석을 통하여 강재-콘크리트 합성 프레임 구조물의 성능을 조사하였다. 본 연구 의 혁신적인 측면은 강재 보와 CFT 기둥의 연결부 사용과 저탄소강과 형상 기억 합금 구성요소의 조합을 활용하 는데 있다. 이러한 새로운 연결부의 목적은 지진 후 건물의 손상과 잔류 흐름을 줄이기 위해 고탄성 형상기억합금 인장부에서 발생하는 교정 작용과 저탄소강의 우수한 에너지 분산 능력을 활용하는 것이다. 연결부의 핀, 전체적인 고정 또는 부분 구속으로 모델링을 할 수 없기 때문에 이러한 구조물들의 해석과 설계는 복잡하여 PR-CFT 연결부 의 전체적인 거동을 알기 위한 수치해석을 위해 정교한 3차원 솔리드 요소로 구성된 유한해석 모델을 개발하였다. 이러한 유한요소 해석으로 얻은 결과를 바탕으로 스프링 요소를 이용하여 간단한 연결부 모델링을 공식화 시켰다. 반복 하중을 가하여 전체 프레임 구조물의 거동을 확인하였고 3D 유한요소 해석을 통하여 단순 거동을 비교하였 다.

Ag spot-coated Cu nanopowders were synthesized by a hydrothermal-attachment method (HA) using oleic acid capped Ag hydrosol. Cu nano powders were synthesized by pulsed wire exploding method using 0.4 mm in diameter of Cu wire (purity 99.9%). Synthesized Cu nano powders are seen with comparatively spherical shape having range in 50 nm to 150 nm in diameter. The oleic acid capped Ag hydrosol was synthesized by the precipitation-redispersion method. Oleic acid capped Ag nano particles showed the narrow size distribution and their particle size were less than 20 nm in diameter. In the case of nano Ag-spot coated Cu powders, nanosized Ag particles were adhered in the copper surface by HAA method. The components of C, O and Ag were distributed on the surface of copper powder.

톱다리개미허리노린재의 집합페로몬은 수컷에 의해 분비되며 같은 종의 성충과 약충을 유인하는 것으로 알려져 있다. 현재 합성된 집합페로몬을 이용한 유인트랩이 널리 이용되고 있다. 본 연구에서는 합성된 집합페르몬에 대한 톱다리개미허리노린재 성충과 약충의 반응을 먹이 섭식 조건을 달리하여 Y자 후각계(Y-tube olfactometer)를 이용하여 조사하였다. Y자 후각계 끝의 공기와 페로몬이 혼합되는 지점에서 교미경험이 없고 수분만 공급받은 성충의 최초 반응률은 수컷에서 84%, 암컷에서 90%이었다. 그리고 반응한 암컷과 수컷의 69%가 Y자 후각계의 집합페로몬 쪽으로 이동하였다. 제2령 약충에서는 수분과 설탕물을 공급받은 경우 최초 반응률은 각각 60과 56%이었고 그 중 각각 63과 64%가 집합페로몬 쪽을 선택하였다. 다만 콩을 먹이로 충분히 공급받은 제2령 약충은 최초 반응률이 34%로 낮았고 집합페로몬 쪽으로 유인된 비율도 31%로 낮았다. 따라서 톱다리개미허리노린재 약충이 먹이를 섭식한 후에는 집합페로몬에 적게 유인되는 것을 알 수 있다.

In this study we experimented that how polyurethane effect to acrylic-polyurethane resin in Full-Grain leather coatings. First of all, we consummated waterborne acrylic emulsion and waterborne polyurethane resin, Than we prepared F.G leathers which were coated by acrylic resin and acrylic-polyurethane resins. According to measured data for solvent resistance, acrylic resin and acrylic-polyurethane resins had good property. Sample a(WAC) had most low strength(2.10kgf/mm2) and sample d(WAC 93 : WPU 7) had most high strength(3.41kgf/mm2). Also we knew that most good property of abrasion is d(47.4 mg). In elongation case, a(WAC) had most good result(645 %) in this experiment.

Antioxidant agent, 1,1,3-tris(2-methyl-4-hydroxy-5-tert-butylphenyl)butane were prepared and investigated the antioxidant activity on recycled rubber mat manufactured with waste tire powder. Mechanical properties of rubber mat are influenced by many factor such as compounding ingredients and state of cure, process of rubber, and fillers. Our study aim is to investigate influence of antioxidant activities on ozone cracking and the thermal aging time. In this work, the degradation of recycled rubber mat was studied and suggested mechanism to involve two-type of degradation, thermal aging and cracking both of which can be contained antioxidant or non-antioxidant agent.

The pearlesent pigment has received attention in a diversity of fields like cosmetics, inks, paints and so on. Ferric Ferrocyanide, one of the nano sized pearlescent pigment, is a kind of surface modification pigment that covers a metal oxidized substance or a coloring agent with uniform thickness. Characteristics of pearlescent pigment are various interference color, intense gloss effect and a three-dimensional effect. We synthesised the pearlesent pigment that ferric ferrocyanide can be deposited on the titania/mica surface by hydrothermal synthesis method. The process parameters are concentration of precursor, controlling pH and reaction temperature. The optimun conditions is that amount of iron(III) chloride hexahydrate is 3.1 wt% and amount of potassim ferrocynide trihydrate is 3.6 wt% in the started pH 4.5 at 70℃. The coating rate and coating efficiency of ferric ferrocyanide was about 1.47 % and 96.7 %, respectively. The synthesised pearlesent pigment was characterized by SEM, XRD, FT-IR and EDS.

Caffeic acid is a kind of phytochemicals occurred in coffee, which is worked as a carcinogenesis restrainer and antioxidants on the human body. In this study, as one type of caffeic acid derivatives, methoxypolyethylene glycol caffeate(MPC) was synthesized by the esterification between caffeic acid and methoxypolyethylene glycol with N,N'-dicyclohexyl carbodiimide, 4-dimethylamino pyridine. The synthesized product was confirmed by using FT-IR and 1H-NMR, thin-layer chromatography. And these compound was investigated as antioxidant, Tyrosinase hindrance and skin moisturizers. In the free radical scavenging study, antioxidant effect of MPC was averagely high than the red ginseng extract that be used as a natural antioxidants. The result of Tyrosinase anti-activity test was better than embryo bud of rice extract at low concentration. At the iNOS anti-activity tested by using Raw 264.7 cell, and confirmed anti-inflammatory function. For the MPC handled with sodium lauryl sulfate, was tested for the skin moisture content and skin moisture loss.