본 연구는 다종 위성 자료를 활용한 해수면온도 합성 기법에 대한 연구이다. 현재 많은 연구자들이 사용하고 있는 NGSST 알고리듬은 위성에 따른 정확도를 고려하지 않고 시 공간 상관도만을 계산하여 해당 픽셀의 값을 추정한다. 본 연구에서는 위성 센서별로 가지고 있는 정확도를 추가로 고려한 해수면온도 합성기법을 제안하고 기존 알고리듬과의 비교를 수행하였다. 합성장을 산출하는데 사용된 센서는 적외 센서인 MODIS, AVHRR 그리고 마이크로파 센서인 AMSR-E를 사용하였고, 2011년 4월 4일을 기준으로 5 km의 공간해상도를 갖는 일일 해수면 온도 합성장을 비교하였다. 부이와의 비교 결과, 기존 방법(NGSST Method)과 제안 방법(New Method)에 의한 표준편차는 각각 0.15℃와 0.12℃이었다. 또한 기존 방법보다 제안 방법에 의한 해수면온도 값은 연안을 제외한 대부분의 해역에서 다소 높게 산출이 되었다. 현 단계에서 정량적인 평가는 어렵지만, 본 연구를 통하여 해수면온도 합성기법에 대한 연구 방향이 제시되었다고 판단된다.

The conversion of coal fly ash into zeolites contributes to the mitigation of environmental problems and turns this by-product into useful material. In this work, zeolitic sorbents for CO₂ adsorption were prepared by waste fly ash from Boryeong coal power plants through the alkali fusion method including hydrothermal treatment at various ratios of NaOH/FA and NaAlO₂/FA. In addition, in order to improve the adsorption capacity for CO₂ molecules a few metal cations were impregnated into the synthesized zeolitic sorbents through the ion exchange. The fusion step could decompose the fly ash to very small amorphous particulate zeolite forms. The fly ash was converted into Na-P1 type with 0.5 NaOH/FA and Na-A type from the ratio of 0.53, NaAlO₂/FA. Although the crystallinity of Na-A increased with increasing temperature, Na-A was transformed into sodalite at 140℃. Thus, the optimum reaction temperature was determined to be 100℃. Alkali metal and alkaline earth metal cations were impregnated into the synthesized zeolite Na-P1 and Na-A through ion exchanged method. The completed zeolitic sorbents were applied to adsorption the CO₂. As a result of the examination, Ca²⁺ was found to be the best for CO₂ adsorption owing to its electrostatic interactions and acid-base surface properties.

본 연구에서는 신형상 층고절감형 합성보에 대한 최적단면을 도출하기 위해 단면성능 계산 프로그램을 개발하여 단면성능에 대해 비교 분석을 하였다. 신형상 합성보는 상부 플랜지 하부에 바닥시스템이 위치하여 전통적인 공법 에 비해 층고절감의 효과와 최적단면으로 설계시 공기의 단축과 비용의 절감은 물론 물량의 감소를 기대 할 수 있 다. 그러나 단면은 기존 H형강 보와 달리 상하 비대칭으로 중립축의 위치가 중앙에 위치하지 않기 때문에 상하연 단에 대한 단면계수가 같지 않게 된다. 이에 따른 상하플랜지 판요소의 두께비에 따른 매개 변수적 분석이 요구된 다. 따라서, 본 연구에서는 단면의 상부 플랜지 두께에 대한 하부 플랜지 두께의 비에 따른 중립축위치, 단면계수의 변화추이를 분석하여 최적단면을 도출하는데 주목적을 두었다.

WCl6-EtAlCl2 촉매계를 이용하여 비교적 큰 분자량을 갖는 폴리(페닐아세틸렌)을 합성하였다. 중합반응이 잘 진행되었으며 중합수율은 81%였다. 합성한 폴리(페닐아세틸렌) 분자구조를 NMR(1H-,13C-), IR, UV-visible, 원소분석 등으로 분석한 결과 페닐 치환기를 갖는 공액구조 고분자가 합성되었음을 확인할 수 있었다. 아울러 332 nm의 빛으로 여기시킬 경우 PL 최대 peak는 424 nm에서 관찰되었는데, 이는 2.93 eV의 광 에너지에 해당한다. 이 고분자의 순환 전압전류 그림은 도핑과 탈도핑사이에서 비가역적인 전기화학적 거동을 보여주었다. 이 고분자의 전기화학적 과정이 매우 안정하였으며, 스캔속도에 따른 산화전류 밀도 실험으로부터 이 고분자의 산화-환언 과정은 확산-제어과정에 따르는 것으로 분석되었다.

Al2TiO5 has a high refractive index and good solubility of the chromophore in the Al2TiO5 lattice, which allowsthis structure to be a good candidate for the development of new ceramic pigments. However, pure Al2TiO5 is well knownto decompose on firing at 900~1100oC. However, this process can be inhibited by the incorporation of certain metal cationsinto its crystalline lattice. In this study, the synthesis of gray ceramic pigment was performed by doping cobalt on the Al2TiO5crystal structure. The Al2TiO5 was synthesized using Al2O3 and TiO2, and doped with Co3O4 as a chromophore material. Inorder to prevent the thermal decomposition during the cooling procedure, MgO was added to samples by 0.05mole, 0.1mole,and 0.15mole as a stabilizer. The samples were fired at 1500oC for 2 hours and cooled naturally. The crystal structure, solubilitylimit, and color of the synthesized pigment were analyzed using XRD, Raman spectroscopy, UV, and UV-vis. Al2O3 wasavailable for the formation of CoAl2O4, which should also be considered in order to explain the small amount of this phasedetected in the sample with the higher Co2+ content (≥0.03mole). It was found that the solubility limit of Co2+ in the Al2TiO5crystal was 0.02mole% through an analysis of Raman spectroscopy. Through the addition of a pigment with 0.02mole% ofCo2+ to lime-barium glaze, stabilized gray color pigments with 66.54, −2.35, and 4.68 as CIE-L*a*b* were synthesized.

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.

Zr-Ti alloy powders were successfully synthesized by magnesium thermal reduction of metal chlorides. The evaporated and mixed gasses of were injected to liquid magnesium and the chloride components were reduced by magnesium leading to the formation of . The released Zr and Ti atoms were then condensed to particle forms inside the mixture of liquid magnesium and magnesium chloride, which could be dissolved fully in post process by 1~5% HCl solution at room temperature. By the fraction-control of individually injected and gasses, the final compositions of produced alloy powders were changed in the ranges of Zr-0 wt.%~20 wt.%Ti and their purity and particle size were about 99.4% and the level of several micrometers, respectively.

Cemented tungsten carbide has been used in cutting tools and die materials, and is an important industrial material. When the particle size is reduced to ultrafine, the hardness and other mechanical properties are improved remarkably. Ultrafine cemented carbide with high toughness and hardness is now widely used. The objective of this study is synthesis of nanostructured WC-Co powders by liquid phase method of tungstate. The precursor powders were obtained by freezen-drying of aqueous solution of soluble salts, such as ammonium metatungstate, cobalt nitrate. the final compositions were WC-10Co. In the case of liquid phase method, it can be observed synthesis of WC-10Co. The properties of powder produced at various temperature, were estimated from the SEM, BET and C/S analyser.

Nanostructured cobalt materials have recently attracted considerable attention due to their potential applications in high-density data storage, magnetic separation and heterogeneous catalysts. The size as well as the morphology at the nano scale strongly influences the physical and chemical properties of cobalt nano materials. In this study, cobalt nano particles synthesized by a a polyol process, which is a liquid-phase reduction method, were investigated. Cobalt hydroxide (Co(OH)2), as an intermediate reaction product, was synthesized by the reaction between cobalt sulphate heptahydrate (CoSO4·7H2O) used as a precursor and sodium hydroxide (NaOH) dissolved in DI water. As-synthesized Co(OH)2 was washed and filtered several times with DI water, because intermediate reaction products had not only Co(OH)2 but also sodium sulphate (Na2SO4), as an impurity. Then the cobalt powder was synthesized by diethylene glycol (DEG), as a reduction agent, with various temperatures and times. Polyvinylpyrrolidone (PVP), as a capping agent, was also added to control agglomeration and dispersion of the cobalt nano particles. The optimized synthesis condition was achieved at 220˚C for 4 hours with 0.6 of the PVP/Co(OH)2 molar ratio. Consequently, it was confirmed that the synthesized nano sized cobalt particles had a face centered cubic (fcc) structure and with a size range of 100-200 nm.

In this study we experimented that how chain extension influences to waterborne urethane-acrylic hybrid resin for leather garment coatings. We knew that polyurethane-acrylic hybrid resins had 5 grades of solvent resistance. Tensile strength measured in the polyurethane-acrylic resin(EDA 5.37 g, 1.928 kgf/mm2) had the most strong strength. Also polyurethane-acylic hybrid resin(EDA 5.37 g. 30.2 mg. loss) had better result than other hybrid resins. EDA contents higher, we obtained low elongation and low flexibility. In this result, chain extension of waterborne polyurethane-acrylic hybrid resin showed the effect in leather coating with ratio of EDA.

Coumarin derivatives were shown to possess valuable pharmacological properties such as anticancer/anti carcinogenic, anti-inflammatory, anti helicobacter, anti genotoxic, neuroprotective and dietary effect. In this study, novel coumarin derivatives structurally related to 7-geranyloxycoumarin were effectively synthesised in good yields by Cs2CO3/acetonitrile in mild condition. The synthesis of geranyloxycoumarin derivatives in weak base(Na2CO3, K2CO3, Cs2CO3 etc)/CH3CN at room temperature obtained in good yield. On the other hand, the reaction of geranyloxycoumarin formation in strong base(NaOH, KOH, CsOH etc)/CH3CN at reflux condition obtained in low yield.

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.

Cationic gemini-surfactant, namely 1,4-butane-bis(N-alkanoyloxyethyl-N,Ndimethyl)-diammonium bromide was synthesized and their inhibition effect on corrosion of mild steel in 1 M HCl solution was tested by weight loss method. The synthesized product was confirmed by FT-IR and 1H-NMR spectroscopy. Surface tensions were measured by surface tensiometer Sigma 70. Their c.m.c. values evaluated by surface tension method was 4.1×10-5~5.4×10-5 mol/L. The Krafft point of the these surfactants were 〈0~10.7℃. The emulsifying properties of synthesized cationic gemini surfactants and sodium dodecyl sulfate (SDS), tetradecyl trimethyl ammonium bromide (TTAB) was investigated. Of these, 1,4-butane-bis(N-lauroyloxyethyl-N,N-dimethyl)- diammonium bromide, CGL 14-4-14 has been confirmed as a good emulsifier. The inhibition efficiency increases by increasing cationic gemini surfactant concentration. As a result, these surfactants are expected to be applied as corrosion inhibitors.

현재 강재와 콘크리트를 합성화 시키는 방법으로 대표적인 것이 스터드를 이용하는 것이다. 그러나 이 방법을 강합 성 기둥에 적용할 경우에 용접량이 많아져 이로 인하여 강재의 성능이 변하여 국부좌굴로 유도될 가능성이 매우 크다. 외부가 구속된 CFT 부재나 내부 구속 중공 CFT 부재 그리고 내부가 강관으로 내부 구속 중공 RC 부재에 적 용할 경우에 합성 거더에 비하여 강재와 콘크리트가 분리되려는 인발력 대신 슬립에 의한 분리현상이 더 크게 발 생한다. 이렇기 때문에 스터드의 높이 보다는 콘크리트와 강재가 합성되는 면적을 넓혀주는 것이 더 필요하다. 이 러한 목적을 달성하기 위하여 일정부분 강관에 용접을 하여 부착을 하고 ㄷ자 형으로 제작된 슬립앵커의 철근이 콘크리트 속에 삽입되어 강재와 콘크리트의 일체 거동성을 높였다. 이러한 방법의 경우에는 곡률을 가진 강구조물 등에 적용될 경우 큰 효과를 발휘할 것으로 판단된다. 본 연구에서는 제안된 슬립앵커를 H빔에 설치를 하여 축하 중을 가하는 Push-over Test를 통하여 거동 특성을 분석하였다.

[ ] a cathode material for lithium rechargeable batteries, was prepared using recycled . First, the cobalt hydroxide powders were separated from waste WC-Co hard metal with acid-base chemical treatment, and then the impurities were eliminated by centrifuge method. Subsequently, powders were prepared by thermal treatment of resulting . By adding a certain amount of and , the was obtained by sintering for 10 h in air at . The synthesized particles were characterized by X-ray diffraction (XRD) and Scanning Electron Microscope (SEM) analysis.

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).

Spherical nanosized cobalt powder with an average size of 150-400 nm was successfully prepared at room temperature from cobalt sulfate heptahydrate (). Wet chemical reduction method was adopted to synthesize nano cobalt powder and hypophosphorous acid () was used as reduction agent. Both the HCP and the FCC Co phase were developed while concentration ranged from 0.7 M to 1.1 M. Secondary phase such as and were also observed. Peaks for the crystalline Co phase having HCP and FCC structure crystallized as increasing the concentration of , indicating that the amount of reduction agent was enough to reduce . Consequently, a homogeneous Co phase could be developed without second phase when the ratio exceeded 7.

We have synthesized bluish-green, highly-efficient BaSi2O2N2:Eu2+ and (Ba,Sr)Si2O2N2:Eu2+ phosphors through aconventional solid state reaction method using metal carbonate, Si3N4, and Eu2O3 as raw materials. The X-ray diffraction (XRD)pattern of these phosphors revealed that a BaSi2O2N2 single phase was obtained. The excitation and emission spectra showedtypical broadband excitation and emission resulting from the 5d to 4f transition of Eu2+. These phosphors absorb blue light ataround 450nm and emit bluish-green luminescence, with a peak wavelength at around 495 nm. From the results of anexperiment involving Eu concentration quenching, the relative PL intensity was reduced dramatically for Eu=0.033. A smallsubstitution of Sr in place of Ba increased the relative emission intensity of the phosphor. We prepared several white LEDsthrough a combination of BaSi2O2N2:Eu2+, YAG:Ce3+, and silicone resin with a blue InGaN-based LED. In the case of onlythe YAG:Ce3+-converted LED, the color rendering index was 73.4 and the efficiency was 127lm/W. In contrast, in theYAG:Ce3+ and BaSi2O2N2:Eu2+-converted LED, two distinct emission bands from InGaN (450nm) and the two phosphors (475-750nm) are observed, and combine to give a spectrum that appears white to the naked eye. The range of the color renderingindex and the efficiency were 79.7-81.2 and 117-128 lm/W, respectively. The increased values of the color rendering indexindicate that the two phosphor-converted LEDs have improved bluish-green emission compared to the YAG:Ce-converted LED.As such, the BaSi2O2N2:Eu2+ phosphor is applicable to white high-rendered LEDs for solid state lighting.

ZnO nanorods for gas sensors were prepared by a hydrothermal method. The ZnO gas sensors were fabricated on alumina substrates by a screen printing method. The gas-sensing properties of the ZnO nanorods were investigated for CH4 gas. The effects of growth time on the structural and morphological properties of the ZnO nanorods were investigated by X-ray diffraction and scanning electron microscope. The XRD patterns of the nanocrystallized ZnO nanorods showed a wurtzite structure with the (002) predominant orientation. The diameter and length of the ZnO nanorods increased in proportion to the growth time. The sensitivity of the ZnO sensors to 5 ppm CH4 gas was investigated for various growth times. The ZnO sensors exhibited good sensitivity and rapid response-recovery characteristics to CH4 gas, and both traits were dependent on the growth time. The highest sensitivity of the ZnO sensors to CH4 gas was observed with the growth time of 7 h. The response and recovery times were 13 s and 6 s, respectively.