Research is being actively conducted on the continuous thin plate casting method, which is used to manufacture magnesium alloy plate for plastic processing. This study applied a heat transfer solidification analysis method to the melt drag process. The heat transfer coefficient between the molten magnesium alloy metal and the roll in the thin plate manufacturing process using the melt drag method has not been clearly established until now, and the results were used to determine the temperature change. The estimated heat transfer coefficient for a roll speed of 30 m/min was 1.33 × 105 W/m2·K, which was very large compared to the heat transfer coefficient used in the solidification analysis of general aluminum castings. The heat transfer coefficient between the molten metal and the roll estimated in the range of the roll speed of 5 to 90 m/min was 1.42 × 105 to 8.95 × 104 W/m2·K. The cooling rate was calculated using a method based on the results of deriving the temperature change of the molten metal and the roll, using the estimated heat transfer coefficient. The DAS was estimated from the relationship between the cooling rate and DAS, and compared with the experimental value. When the magnesium alloy is manufactured by the melt drag method, the cooling rate of the thin plate is in the range of about 1.4 × 103 to 1.0 × 104 K/s.

In this study, the effect of thermal grease and heat sink material of cooler on CPU temperature was measured and compared with LinX(v0.9.6) and HWMonitor.When the computer is booted without thermal grease applied, the CPU temperature rises rapidly, and the CPU temperature reaches 100℃ after 60 seconds for aluminum heat sink and 140 seconds for copper heat sink. The CPU temperature is lower as the thermal conductivity coefficient of thermal grease is higher, and the CPU temperature is lower when the thermal conductivity coefficient of the cooler is higher. In addition, when using a thermal grease and a heat sink with a high coefficient of thermal conductivity, the cooler rpm can be lowered, which is considered to be advantageous in terms of system stability and energy saving.

The electrical properties of a laminated SMD type PTC thermistor for microcircuit protection were investigated as a function of polymer blowing agent addition. Green ceramics for multilayered BaTiO3-based PTCRs were formed by doctor blade method of barium titanate powders; we successfully laminated the sintered ceramic chips to obtain 10 layer chip PTCRs with PTC effect. The sintered density increases with increasing sintering temperature. The electrical properties of the sintered samples were strongly dependent on the calcination and addition of a polymer blowing agent. When BaTiO3 powders containing 0.2 mol% of Y2O3 were calcined at 1000˚C for 2 hrs, the resistivity jump was of 1-2 orders of magnitude. The resistivity at room temperature increases according to the polymer blowing agent addition. Also, the sample using the calcined powder showed a lower resistivity than that of the sample prepared using powders without calcinations. With an increase in the OBSH, the magnitude of the resistivity jumped as a function of the temperature increase. The resistivity of the sintered bodies after the addition of 0.5 wt% polymer blowing agent at 1290˚C for 2 h was shown to be about 8.5Ω·cm; the jump order of the sintered bodies was shown to be on the order of 102.

The influences of Na and K content on the crystal phase, the microstructure and the electrical property of BaTiO3-based thermistors was found to show typical PTC effects. The crystal phase of powder calcined at 1000˚C for 4hrs showed a single phase with BaTiO3, and the crystal structure was transformed from tetragonal to cubic phase according to added amounts of Na and K. In XRD results at 43˚~47˚, the (Ba0.858Na0.071K0.071)(Ti0.9985Nb0.0015)O3-δ showed (002) and (200) peaks but the (Ba0.762Na0.119K0.119)(Ti0.9975Nb0.0025)O3-δ showed (002), (020) and (200) peaks. In sintered bodies, those calcined at 600˚C rather than at 1000˚C were dense, and for certain amounts of Na and K showed rapid decreases in grain size. In relative permittivity, the curie temperature due to the transformation of ferroelectric phase rose with added Na and K but decreased in terms of relative permittivity. In the result of the R-T curve, the sintered bodies have curie temperatures of about 140˚C and the resistivity of sintered bodies have scores of Ω·cm; the jump order of sintered bodies was shown to be more than 104 in powder calcined at 1000˚C.

The microstructure and positive temperature coefficient of resistivity (PTCR) characteristics of 0.1mol%Na2Ti6O13doped 0.94BaTiO3-0.06(Bi0.5Na0.5)TiO3 (BBNT-NT001) ceramics sintered at various temperatures from 1200oC to 1350oC wereinvestigated in order to develop eco-friendly PTCR thermistors with a high Curie temperature (TC). Resulting thermistors showeda perovskite structure with a tetragonal symmetry. When sintered at 1200oC, the specimen had a uniform microstructure withsmall grains. However, abnormally grown grains started to appear at 1250oC and a homogeneous microstructure with large grainswas exhibited when the sintering temperature reached 1325oC. When the temperature exceeded 1325oC, the grain growth wasinhibited due to the numerous nucleation sites generated at the extremely high temperature. It is considered that Na2Ti6O13 isresponsible for the grain growth of the 0.94BaTiO3-0.06(Bi0.5Na0.5)TiO3 ceramics by forming a liquid phase during the sinteringat around 1300oC. The grain growth of the BBNT-NT001 ceramics was significantly correlated with a decrease of resistivity.All the specimens were observed to have PTCR characteristics except for the sample sintered at 1200oC. The BBNT-NT001ceramics had significantly decreased ñrt and increased resistivity jump with increasing sintering temperature at from 1200oC to1325oC. Especially, the BBNT-NT001 ceramics sintered at 1325oC exhibited superior PTCR characteristics of low resistivityat room temperature (122Ω·cm), high resistivity jump (1.28×104), high resistivity temperature factor (20.4%/oC), and a highTc of 157.9oC.

아라고나이트는 탄산칼슘(CaCO3)의 동질이상 중 하나이며, 해양 생태계를 포함한 다양한 환경에서 생물학적 및 이화학적 침전 과정을 통해 형성된다. 이러한 아라고나이트의 형성 및 성장뿐만 아니라 아라고나이트 내 스트론튬(Sr)과 같은 미량원소의 치환 특성은 화학종의 농도와 온도와 같은 핵심 인자들에 의해 많은 영향을 받는다. 본 연구에서는 해양 생태계와 유사한 용액 온도와 아라고나이트에 대한 이 용액의 다양한 포화도 조건에서 아라고나이트 내 Sr 병합 특성이 규명되었다. 반응 용액의 주입속도(0.085-17 mL/min), 반응 용액의 이온 농도([Ca]=[CO3] 0.01-1M), 혼합 용액의 온도(5-40 oC)의 다양한 실험 조건에서 컨스턴트-에디션 (constant-addition) 방법을 통해 순수한 아라고나이트가 합성되었다. 또한, 모든 Sr 병합 실험 조건(0.02-0.5 M, 15-40 oC)에서도 순수한 아라고나이트가 형성되었다. 합성된 아라고나이트의 결정도와 결정크기는 포화도 및 온도가 증가함에 따라 상대적으로 더 크게 증가하며 아라고나이트 결정이 더 많이 성장하였음을 지시하였다. 그러나 BET-비표면적을 이용하여 계산된 결정성장속도는 결정 형상 변화에 크게 영향을 받는 것으로 나타나 해석에 주의가 요구된다. 아라고나이트 내 Sr의 분배계수(KSr)는 반응이온의 농도가 0.02에서 0.5 M로 증가할 때 2.37에서 1.57로, 온도가 15에서 40˚C로 증가할 때 1.90에서 1.54로 감소하였으며, 모든 조건에서 KSr 값이 1보다 높게 관찰되었다. 이러한 결과는 KSr가 결정성장속도와 역의 상관관계로서 아라고나이트 내 Sr 병합이 호정성 관계임을 나타낸다.