To solve the common problems of concrete preparation in low-temperature environments, calcium formate (C2H2O4Ca), anhydrous sodium sulfate (Na2SO4), triethanolamine (C6H15O3N), calcium bromide (CaBr2), and triisopropanolamine (C9H21NO3) are selected as early strength agents and mixed with C40 concrete in different dosages under low-temperature environments of 5 oC and 10 oC to develop a high-efficiency low-temperature compound early strength agent based on the effect of single-doped early strength agents. The effects of the compound early strength agent on the early strength of the concrete, the cement paste setting time, and cement fluidity at 5 oC and 10 oC are investigated, and the corresponding reaction mechanism is discussed from the perspective of micro-products. The best compound early strength agent ratio is found to be 2% of calcium formate + 0.08 % of TEA (C6H15O3N). The compound early strength agent effectively promotes the formation of hydration products, such as Ca(OH)2 and C-S-H gel. In comparison with the control group, the strength of the concrete cured for 18 h, 1 d, 3 d, and 7 d under simulated natural conditions at 5 oC increases by 700%, 540%, 11.4 % and 10 %, respectively, whereas at 10 oC, the corresponding values are 991%, 400%, 19.6 % and 11 %, respectively. The strength of the concrete at each age is close to the normal temperature standard of the curing strength. The addition of the compound early strength agent causes a reduction in cement fluidity and initial and final setting times, and also yields a good effect on the porosity of the early concrete.
입자 크기가 약 16 및 5 nm인 두 다른 크기의 TiO2 나노입자들과 titanium tetraisopropoxide (TTIP) binder 와 ethanol 용매만으로 제조된 코팅액을 사용하여 130 oC 저온 열처리로 ITO/PEN substrate 위에 메조다공성 TiO2 박막들을 형성하였다. 이들 TiO2/ITO/PEN 박막들을 활용한 유연 염료감응 태양전지들을 제작하여 광변환 특성을 비교 연구하였다. 크기가 다른 두 TiO2 나노입자들을 각각 단독으로 사용하여 제작된 cell들의 경우에 크기가 16 nm 인 TiO2 나노입자 cell이 5 nm인 나노입자 cell에 비해 박막의 porosity가 훨씬 크고 같은 질량에서 표면적이 훨씬 넓어 광변환 효율이 훨씬 높으나 염료 흡착량에 대해 상대적으로 작은 광전류는 입자간의 연결성에 기인되며 큰 입 자에 작은 입자를 10% 정도 혼합한 경우에 표면적 증가와 함께 입자간의 연결성을 강화시켜 큰 입자 단독으로 제작 된 cell에 비해 광변환 효율이 크게 증가됨을 확인하였다.
The organic binder-free paste for dye-sensitized solar cell (DSSC) has been investigated using peroxo titanium complex. The crystal structure of TiO2 nanoparticles, morphology of TiO2 film and electrical properties are analyzed by X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM), Electrochemical Impedance Spectra (EIS), and solar simulator. The synthesized TiO2 nanopowders by the peroxo titanium complex at 150, 300, 400˚C, and 450˚C have anatase phase and average crystal sizes are calculated to be 4.2, 13.7, 16.9, and 20.9 nm, respectively. The DSSC prepared by the peroxo titanium complex binder have higher Voc and lower Jsc values than that of the organic binder. It can be attributed to improvement of sintering properties of TCO/TiO2 and TiO2/TiO2 interface and to formation of agglomerate by the nanoparticles. As a result, we have investigated the organic binder-free paste and 3.178% conversion efficiency of the DSSC at 450˚C.
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.
Alloys of nylon(PA6) and ethylene-propylene-diene polymer, modified with maleic anhydride(MEPDM) were prepared using a melt kneading process. This study focuses on the effects of the content of MEPDM in PA6 blend on the mechanical and thermal properties of such blends where MEPDM is the dispersed phase. Mechanical properties were examined by stress-strain measurements and impact strength test. Both impact strength of PA6/MEPDM at room temperature and at -20℃ were improved up to 400-550% with the amounts of MEPDM. However, PA6/MEPDM containing 3-5 wt% of MEPDM showed the about 700kgf/m2 of the maximum tensile strength but 8.5 % of the lowest elongation. For certain compositions of PA6 with rubbery MEPDM, the interesting reduction of elongation is caused by the reaction of the polyamide amine end groups with maleic anhydride portion in MEPDM, that provided a reinforcement in the PA6 matrix. In addition, the introduction of antistatic agent on the surface of alloys causes significant reduction of their surface electrostatic resistance.
The surface of poly(ethylene naphthalate) film applicable to high temerature insulator for convection microwave oven was modified with silicone coating solutions in the presence of silane crosslinking agent. The structure and properties of the PEN films were investigated by using Fourier transform IR spectroscopy, viscometry, microscopy, and tensile tests. The experimental results showed that the coating with silicone enhanced thermal stability up to 200℃, and slightly lowered the tensile strength and elongation of the PEN films. Judging from dimensional stability results the silicone coated PEN films can not be used for higher temperature insulator above 230℃. Serious dimensional contraction of films was obtained during heat treatment at 250℃ even for 1h. However, the surface of those films still have same chemical structure of silicones. Therefore, If we use PEN film prestretched at 230℃ as base one it will be possible to prepare a high temperature insulator up to 230℃. Conclusively, a silicone coated PEN film can be suitable for the application to convection microwave oven door insulator at high temperature up to 230℃.
당뇨병 환자의 혈당치 측정을 위하여 폴리우레탄으로 만들어진 진단막을 제조하였다. 플라즈마와 혈액속의 글루코오즈의 농도를 변화시켜가며 활성화된 폴리우레탄 진단막을 가지고 680 nm에서의 최종흡광도를 측정하였다. 여러 가지 보관온도에서 3일, 1주, 3주, 5주간 보관 후 온도가 글루코오즈의 농도 측정에 미치는 영향을 조사하였다. 우레탄 진단막의 안정성을 상대습도 80%에서 측정하였다.
This study for preparation of aluminum nitride (AlN) with high purity was carried out by self-propagating high-temperature synthesis method in two different systems, Al-N and Al-N-AlN, with the change of nitrogen gas pressure and dilution factor. On the occasion of Al-N system, unreacted aluminum was detected in the product in spite of high nitrogen pressure, 10 MPa, This may be caused by obstructing nitrogen gas flow to inner part of molten and agglomerate of aluminum, formed in pre-heating zone. In Al-N-AlN system, AlN with a purity of 95% or ever can be prepared in the condition of f 0.5, PN2 1 MPa, and the purity can be elevated to 98% over in the condition of f = 0.7 and PN2 = 10 MPa
본 연구에서는 연질 폴리우레탄 발포제 제조에서 여러 발포제와 내부온도, 기계적 물성과의 관계에 대해서 연구, 조사하였다. 발포제로는 물을 주발포제로 하여 보조발포제는 CFC-11(trichlorofluoromethane), HCFC-114b(dichlorofluoroethane), dichloromethane, n-pentane, iso-pentane, cyclopentane을 사용하였다. 기계적 물성을 측정하기 위하여 연질 폴리우레탄 발포제의 밀도가 0.015±0.002g/cm3와 0.024±0.002g/cm3인 두 종류의 발포제를 제조하였다. 연질 폴리우레탄의 발포제의 제조시 발포제별로 내부온도를 측정하였으며, 48시간 경과 후 밀도, 인장강도, 신장율, 인열강도, 압축강도, 압축영구변형률을 측정하였다. 연구 결과 dichloromethane과 cyclopentane이 보조발포제로 가장 적합하였다.
본 연구를 통해서 온도감응성 polyurethane을 제조하여 수분의 투과거동을 검토하고 약물방출조절용 제제로의 적용가능성을 검토하였다. Polyurethane의 기계적 물성 및 Tg는 사용한 polyol의 분자량과 hard segment의 양을 이용하여 조절하였으며 온도증가에 따라 수분의 투과도가 증가함을 알 수 있었다. 따라서 온도변화에 따라 약물의 투과도가 변화하는 온도감응성 약물방충용 재료로 사용 가능성을 확인하였다.
Ti-48AI(at.%) 모재위에 RF magnetron sputtering을 이용하여 AI-21Ti-23Cr(at.%) 조성의 박막을 코팅하였다. RF power 200W, 증착압력 0.8Pa, 증착온도 573k에서 증착된 시편의 가장 우수한 고온재산화성을 나타내었다. 573K에서 증착된 AI-21Ti-23Cr 코팅층은 증착시에는 비정질을 형성하나 산화시험동안 결정화가 진행되며, 표면에는 치밀한 Al2O3층이 형성되었다. 573K에서 코팅된 시편에 대하여 1073K, 1173K 및 1273K에서 100시간동안 등온산화시험을 실시하였다. 무게증량곡선은 모든 온도에서 parabolic law를 따르는 안정된 산화거동을 보였으며 이와같은 산화특성은 표면에 치밀한 Al2O3층이 형성되었기 때문인 것으로 판단된다. 1273K에서 산화시험 후 코팅층의 기지는 고온산화에 따른 AI원자의 소모와 모재로부터의 Ti원자의 확산에 의해 TiAICr상을 형성하였으며, 무게증량은 낮은 온도에 비해 다소 크게 증가하는 경향을 나타내었다.
지르코니아 분말 합성 시 500ppm의 Polyvinyl Alcohort(PVA) 첨가에 의해 입자가 균질하게 분산된 안정된 지르코니아 현탁액을 제조하였다. 이러한 현탁액으로부터 원심분리에 의해 제조된 충진체는 PVA를 첨가하지 않은 시편의 충진체에 비해 기공의 크기가 작은 고밀도의 균질한 충진체였다. 이 충진체를 사용하여 소결한 결과, 지르코니아 소결에 있어서는 비교적 낮은 온도인 1250˚C에서도 상대밀도가 98%인 고밀도의 단사성 지르코니아 소결체를 제조할 수 있었다.