• 대한방사선기술학회지:방사선기술과학
• /
• 제26권3호
• /
• pp.51-57
• /
• 2003

자체 개발한 수소화금속을 이용하여 고속 중성자 방사선을 효율적으로 차폐할 수 있다면 방사선 안전신기술 개발과 확립에 큰 기여를 할 것으로 생각되어 본 연구를 시행하였다. 여러 수소화 안정 금속들을 대상으로 핵적 특성, 단위 부피당 수소원자함유 수 등의 예비평가를 통하여 수소화금속($ZrH_2,\;TiH_2$) 등과 낮은 중성자 흡수 단면적과 높은 에너지 감쇄능력을 고려하여 중수소화 금속($ZrD_2,\;TiD_2$) 등을 추가하여 개발하였다. MCNP 코드를 이용하여 각각의 흡수율과 에너지 감소율을 평가하였다. 전산 모사 계산과 실험과의 비교평가를 위해 실험과 동일한 조건의 모사를 수행하였는데, 즉 중성자 선원은 Cf-252(10 mCi)을 사용하였으며 각 수소화금속의 0, 1, 3, 5 cm 두께를 통과한 중성자속의 강도와 에너지별 분포변화를 계산하였다. 코드 계산을 통해 평가된 $TiH_2/TiD_2,\;ZrH_2,/ZrD_2$ 등의 수소화금속에 대한 중성자 감소율은 각 수소화금속 두께의 증가에 따라 중성자 감소율이 지수적으로 증가함을 보였다. 또한 이 때 중수소 함유 금속, $ZrD_2$과 $TiD_2$는 중성자 흡수에 있어 $ZrH_2$와 $TiH_2$의 각각 보다 적게 나타냈다. 본 연구를 통하여 개발된 수소화금속의 중성자 방사선 차폐에 관한 결과는 과학 기술적으로 많은 인용과 아울러 학술적 연구뿐만 아니라 실제 실용화를 위한 연구의 기초자료로 충분한 활용이 있을 것으로 기대한다.

• 소성∙가공
• /
• 제28권1호
• /
• pp.21-26
• /
• 2019

Direct Laser Melting (DLM) of $Ti-xTiH_2$ (mixing ratio x = 2, 5, 10 wt.%) blended powder is characterized by producing porous titanium parts. When a high energy laser is irradiated on a $Ti-TiH_2$ blended powder, hydrogen gas ($H_2$) is produced by the accompanying decomposition of the $TiH_2$ powder, and acts as a pore-forming and activator. The hydrogen gas trapped in a rapidly solidified molten pool, which generates porosity in the deposited layer. In this study, the effects of a $TiH_2$ mixing ratio and the associated processing parameters on the development of a porous titanium were investigated. It was determined that as the content of $TiH_2$ increases, the resulting porosity density also increases, due to the increase of $H_2$ produced by $TiH_2$. Also, porosity increases as the scan speed increases. As fast solidified melting pools do not provide enough time for $H_2$ to escape, the faster the scan speed, the more the resulting $H_2$ is captured by the process. The results of this study show that the mixing ratio (x) and laser machining parameters can be adjusted to actively generate and control the porosity of the DLM parts.

• 한국수소및신에너지학회논문집
• /
• 제7권1호
• /
• pp.19-28
• /
• 1996

Ti-Mn based hydrogen storage alloy were modified by substituting alloying elements such as Zr, V and Ni in order to design a high capacity MH electrode for Ni/MH rechargeable battery. When V was substituted in Ti-Mn binary system, the crystal structure was maintained as $Cl_4$ Laves phase at a composition of $Ti_{0.2}V_{0.4}Mn_{0.4}$ and $Ti_{0.4}V_{0.2}Mn_{0.4}$ and equilibrium pressure decreased below 1 atm without decreasing hydrogen storage capacity considerably. It was found that Ni should be included in Ti-V-Mn alloy in order to hydrogenate it electrochemically in KOH electrolyte. But substitution of Ni for Mn in Ti-V-Mn system caused the increase of equilibrium pressure above 1atm and decrease of hydrogen storage capacity. Zr was able to increase the reversible hydrogen storage capacity of Ti-V-Mn-Ni alloy without considerable change of hydrogenation properties. The electrochemical discharge capacity of Ti-Zr-V-Mn-Ni system were in the range of 350 - 464mAh/g and among them $Ti_{0.8}Zr_{0.2}V_{0.5}Mn_{0.5}Ni_{1.0}$ alloy had $Cl_4$ Laves single phase and very high electrochemical discharge capacity of 464mAh/g.

• 한국수소및신에너지학회논문집
• /
• 제5권2호
• /
• pp.73-79
• /
• 1994

The hydrogenation behavior of Ti-Ni powders prepared by mechanical alloying in a high energy ball mill have been investigated by P-C isotherm curves, DSC(differential scanning calorimetry), X-ray diffractometer, SEM(scanning electron microscope). Amorphous TiNi phase was formed after 10 milling hours. The hydrogen storage capacity gradually decreased as a function of mechanical alloying time. There appears the DSC endothermic peak due to hydrogen evolution of amorphous hydride phase.

• 한국수소및신에너지학회논문집
• /
• 제2권1호
• /
• pp.29-37
• /
• 1990

The effect of pressure cycling of $Zr_{0.9}Ti_{0.1}Cr_{0.7}Fe_{1.3}$ on the hydrogenation properties was investigated using the P-C-Isotherm curves and hydrogen absorption rate curves in the isotherm condition. The reversible hydrogen absorption capacity was decreased about 45 % after 3300 cycles. In the case of activated sample, the rate controlling steps of hydriding reaction changed from the surface reaction to the hydrogen diffusion process through hydride phase sequentially as reaction proceeded. After 3300 cycles, the sequential change of rate controlling step was same as activated one. However, the hydrogen absorption rate significantly decreased. It is suggested that the degradation of $Zr_{0.9}Ti_{0.1}Cr_{0.7}Fe_{1.3}$ can be interpreted with the formation of $ZrFe_3$ phase at the particle surface.

• 한국수소및신에너지학회논문집
• /
• 제16권1호
• /
• pp.92-101
• /
• 2005

[ $Li_3AlH_6$ ] (5.6wt% theoretical hydrogen storage capacity) powders with and without Ti-containing dopants have been successfully synthesized by mechanochemical reaction near room temperatures from mixtures of LiH and $LiAlH_4$ powders. It has been observed that single phase $Li_3AlH_6$ could be obtained within 2-3 hours of milling, but the addition of reactive $TiCl_2\;or\;TiCl_3$ to the starting mixtures. caused partial decomposition of $LiAlH_4$ into LiCl and free Al with gaseous $H_2$. By addition of these reactive dopants to the as-synthesized $Li_3AlH_6$, this problem could be solved. The addition of 2 mol% $TiCl_2\;or\;TiCl_3\;to\;Li_3AlH_6$ decreased the decomposition start temperature up to 30-50$^{\circ}C$, while that of Ti or $TiH_2$ did not change the thermal decomposition behavior of $Li_3AIH_6$.

• 한국분말재료학회지
• /
• 제23권3호
• /
• pp.235-239
• /
• 2016

This study is performed to fabricate a Ti porous body by freeze drying process using titanium hydride ($TiH_2$) powder and camphene. Then, the Ti porous body is employed to synthesize carbon nanotubes (CNTs) using thermal catalytic chemical vapor deposition (CCVD) with Fe catalyst and methane ($CH_4$) gas to increase the specific surface area. The synthesized Ti porous body has $100{\mu}M$-sized macropores and $10-30{\mu}m$-sized micropores. The synthesized CNTs have random directions and are entangled with adjacent CNTs. The CNTs have a bamboo-like structure, and their average diameter is about 50 nm. The Fe nano-particles observed at the tip of the CNTs indicate that the tip growth model is applicable. The specific surface area of the CNT-coated Ti porous body is about 20 times larger than that of the raw Ti porous body. These CNT-coated Ti porous bodies are expected to be used as filters or catalyst supports.

• 한국수소및신에너지학회논문집
• /
• 제10권4호
• /
• pp.211-217
• /
• 1999

수소저장합금 전극을 이용하는 박막전지의 제조를 위하여, TiNi 수소저장합금박막의 적정제조조건에 대하여 연구하였다. TiNi합금박막은 직류 스퍼터링을 이용하여 제조하였다. 증착변수인 아르곤유속, 타겔-기판거리, 직류 전력량등을 변화시키면서, 증착속도를 조사하였으며, Ti와 Ni의 화학조성비, 결정구조등을 조사하였다. 증착속도는 아프곤유속, 타겔 기판거리와 반비례하였으며, 직류전력량의 증가에는 정비례하여 증가하였다. 상온에서 증착후에는 비정질구조를 나타냈으나, 진공열처리 후에 결정질로 바뀌었다.

• 한국수소및신에너지학회논문집
• /
• 제8권4호
• /
• pp.181-185
• /
• 1997

The electrochemical properties of the $AB_2$-type (Zr-Ti-V-Ni-Cr-Co-Mn) metal hydride electrodes prepared by ball milling with $AB_5-type\{(LM)Ni_{3.6}Al_{0.4}Co_{0.7}Mn_{0.3}\}$(LM : Lanthanum-rich mischmetal) alloy powder as a surface activator were investigated. By ball milling with $AB_5$ type alloy powder, the activation of $AB_2$ type metal hydride electrode was accelerated resulting in an increase of discharge capacity from 35% to 85% of the maximum capacity at the first cycle. As the amount of surface activator increased the activation rate increased, whereas the discharge capacity increased with 10wt% and decreased with 20wt% addition of the surface activator. When the amount of the surface activator was kept constant as 10wt%, the discharge capacity and the activation rate increased with ball milling time up to 20 hours. However beyond 20 hours of ball milling time, they decreased drastically due to the nano-crystallization or amorphorzation of the alloy powder.

• 한국항공우주학회지
• /
• 제49권9호
• /
• pp.759-769
• /
• 2021

발사체 추진 시스템에서 Titanium Hydride Potassium Perchlorate (THPP)는 에너지를 인가받으면 gas를 발생시키는 pyrotechnic initiator로써 혹은 NASA Standard Initiator (NSI)의 supplement charge로써 흔히 사용되는 물질이다. 하지만 금속으로 이루어진 복합 화약이 오랫동안 보관이 되면 노화라는 문제에 직면하게 된다. 본 연구에서는 열분석 및 표면분석을 통하여 다양한 습도환경에서 노화된 THPP에 대하여 열역학적 특성의 변화를 확인하였고, 이를 바탕으로 THPP에 대한 전반적인 노화 메커니즘을 구축해내었다. 우선, THPP가 노화됨에 따라 산화제 표면의 균열빈도가 증가하고 길이가 길어졌는데, 이는 열·수분 노화가 공통적으로 산화제의 분해를 초래함을 보여준다. 이때 열 노화된 경우 Viton의 열화 현상이, 수분 노화된 경우 연료의 산화가 더욱 두드러졌다. 또한 실험을 통해 계산된 반응률에 대한 THPP의 화학반응인자의 경우 습도에 따라 크게 달라졌는데, 이는 수분이 THPP의 연소에 상당한 변화를 미쳐 결국에는 수명의 감소로 이어지게 될 것을 시사한다.