• 대한기계학회논문집A
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• 제35권4호
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• pp.439-445
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• 2011

대기오염 등 환경에 대한 관심이 높아지면서 경유차 배출 가스 저감을 위한 최적의 대안으로 최근 세계적으로 천연가스차량의 보급이 크게 확대되고 있는 추세이다. 이러한 추세에도 불구하고 그 안전성에 대해서는 많은 논란을 불러 일으키고 있으며 최근 그 이용에 따른 안전사고 또한 빈번하게 발생하고 있다. 천연가스버스 압력용기 파열 사고는 대중들이 많이 이용한다는 점에서 대형참사로 이어질 수 있는 잠재력을 가지고 있어 그 심각성은 매우 크다고 할 수 있다. 이에 법공학적인 측면에서 좀 더 전문화되고 체계적인 사고조사와 원인 규명을 통해서 사전에 예방대책을 마련함으로써 유사 및 동종재해의 발생을 최소화해야 한다. 본 연구에서는 구조해석을 통한 용기의 설계 검증과 용기의 파손형태 검사 및 재료 물성평가 등을 통해 용기파손에 의한 CNG 차량 폭발 사고에 관한 정확한 사고 원인을 규명함으로써 동일 형태의 차량 안전사고 예방에 기여하고자 한다.

• 한국안광학회지
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• 제1권2호
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• pp.49-55
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• 1996

본 연구에서는 LFPCVD법으로 수소화왼 비정질 탄소(a-C:H) 박막을 제작하였으며, 수소화된 비정질 규소 (a-Si:H)에서 주로 나타나는 지속광전기전도도(PPC) 현상을 a-C:H에서 처음으로 관찰하였다. 관찰된 PPC의 크기는 실온에서 암전기전도도의 3배 이상이며, 수 시간 이상 지속되었다. PPC의 크기는 조광시간이 증가함에 따라서 증가를 하며, 조광온도가 증가함에 따라서는 감소를 하여 $120^{\circ}C$ 이상에서 완전히 사라졌다. 또한 PPC의 붕괴는 확장지수붕괴(Stretched Exponential Decay) 함수로 설명할 수 있었다. 이로 미루어 볼 때 a-C:H에서의 PPC는 시료의 이질성과 밀접한 관련이 있다고 생각된다.

• 한국응용과학기술학회지
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• 제37권5호
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• pp.1200-1207
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• 2020

본 연구에서는 다공성 활성탄소와 금속유기골격체 복합재료 기반의 전극 재료와 "이온젤" 이라고 불리는 고분자 고체 전해질을 이용하여 슈퍼커패시터를 제작 하였으며, 금속유기골격체의 함량에 따른 전기화학적 거동을 관찰하여 보았다. 슈퍼커패시터의 전기화학적 특성은 순환전압전류법(CV), 전기화학적 임피던스 분광법(EIS) 및 전정류 충·방전법(GCD)으로 분석하였으며, 그 결과로, 다공성 활성탄소 대비 금속유기골격체를 0.5 wt% 첨가 하였을 때 가장 높은 전기용량값을 확인 할 수 있었으며, 0.5 wt% 이상의 금속유기골격체의 함유량은 전기화학적 특성 감소에 영향을 주는 것으로 사료되며, 이러한 결과를 바탕으로 제조된 다공성 활성탄소/금속유기골격체 복합재료 기반의 슈퍼커패시터는 다양한 분야에 활용이 가능할 것으로 판단된다.

• 한국전기전자재료학회논문지
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• 제13권9호
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• pp.751-757
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• 2000

The r.f. power effect for Pt doping is investigated on structural and electrochemical properties of amorphous vanadium oxide(V$_2$O$_{5}$) film, grown by direct current (d.c.) magnetron sputtering. Room temperature charge-discharge measurements based on a half-cell with a constant current clearly indicated that the Pt doping could improve the cyclibility of V$_2$O$_{5}$ cathode film. Using glancing angle x-ray diffraction(GXRD) and high-resolution transmission electron microscopy (HRTEM) analysis, we found that the Pt doping with 10W r.f. power induces more random amorphous structure than undoped V$_2$O$_{5}$ film. As the r.f. power of Pt target increases. large amount of Pt atoms incorporates into the amorphous V$_2$O$_{5}$ film and makes $\alpha$-PtO$_2$microcrystalline phase in the amorphous V$_2$O$_{5}$ matrix. These results suggest that the semiconducting $\alpha$-PtO$_2$ microcrystalline phase in amorphous matrix lead to a drastically faded cyclibility of 50W Pt doped V$_2$O$_{5}$ cathode film. Possible explanations are given to describe the Pt doping effect on cyclibillity of the amorphous V$_2$O$_{5}$ cathode film battery. film battery.

• 한국신재생에너지학회:학술대회논문집
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• 한국신재생에너지학회 2009년도 추계학술대회 논문집
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• pp.619-619
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• 2009

Recently, silica nanostructures are widely used in various applicationary areas such as chemical sensors, biosensors, nano-fillers, markers, catalysts, and as a substrate for quantum dots etc, because of their excellent physical, chemical and optical properties. Additionally, these days, semiconductor silica and silicon with high purity is a key challenge because of their metallurgical grade silicon (MG-Si) exhibit purity of about 99% produced by an arc discharge method with high cast. Tremendous efforts are being paid towards this direction to reduce the cast of high purity silicon for generation of photovoltaic power as a solar cell. In this direction, which contains a small amount of impurities, which can be further purified by acid leaching process. In this regard, initially the low cast rice-husk was cultivated from local rice field and washed well with high purity distilled water and were treated with acid leaching process (1:10 HCl and $H_2O$) to remove the atmospheric dirt and impurity. The acid treated rice-husk was again washed with distilled water and dried in an oven at $60^{\circ}C$. The dried rice-husk was further annealed at different temperatures (620 and $900^{\circ}C$) for the formation of silica nanospheres. The confirmation of silica was observed by the X-ray diffraction pattern and X-ray photoelectron spectroscopy. The morphology of obtained nanostructures were analyzed via Field-emission scanning electron microscope(FE-SEM) and Transmission electron microscopy(TEM) and it reveals that the size of each nanosphares is about 50-60nm. Using the Inductively coupled plasma mass spectrometry(ICP-MS), Silica was analyzed for the amount of impurities.

• 한국분말재료학회지
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• 제24권4호
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• pp.308-314
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• 2017

$Fe_3O_4$/Fe/graphene nanocomposite powder is synthesized by electrical wire explosion of Fe wire and dispersed graphene in deionized water at room temperature. The structural and electrochemical characteristics of the powder are characterized by the field-emission scanning electron microscopy, X-ray diffraction, Raman spectroscopy, field-emission transmission electron microscopy, cyclic voltammetry, and galvanometric discharge-charge method. For comparison, $Fe_3O_4$/Fe nanocomposites are fabricated under the same conditions. The $Fe_3O_4$/Fe nanocomposite particles, around 15-30 nm in size, are highly encapsulated in a graphene matrix. The $Fe_3O_4$/Fe/graphene nanocomposite powder exhibits a high initial charge specific capacity of 878 mA/g and a high capacity retention of 91% (798 mA/g) after 50 cycles. The good electrochemical performance of the $Fe_3O_4$/Fe/graphene nanocomposite powder is clearly established by comparison of the results with those obtained for $Fe_3O_4$/Fe nanocomposite powder and is attributed to alleviation of volume change, good distribution of electrode active materials, and improved electrical conductivity upon the addition of graphene.

• 한국지반신소재학회논문집
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• 제12권1호
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• pp.29-38
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• 2013

본 논문에서는 생분해 배수재를 이용한 오염토양 정화기술의 현장적용성을 평가하기 위하여 생분해 배수재의 물리적 특성시험을 수행하였으며, 이를 이용한 현장실험을 통하여 중금속 오염토양의 정화효율을 분석하였다. 두 종류(실린더 코어형, 하모니카형)의 생분해 배수재에 대한 시험결과, 실린더 코어형 배수재의 경우, 한국산업규격 표준시방에서 제시하는 기준치를 모두 만족하였으며, 하모니카형 생분해성 배수재는 실린더 코어형 배수재에 비해 배수성능이 상당히 낮은 결과를 나타내었다. 또한 오염토양 복원시 사용한 세정제로는 자체독성이 적어 생태계에 미치는 영향을 최소화하며, 생물학적 재순환시스템과의 최적인 조건을 지니고 있는 시트르산(ctric acid)을 선정하여 중금속 중 Cd, Cu, Pb을 현장실험 대상 오염물질로 선정 후 실험을 수행하였다. 현장실험은 3가지 설치조건을 고려하여 정화효율을 분석하였으며, 반응물질이 도포된 생분해 배수재를 이용하여 세척제를 주입 추출을 동시에 수행한 경우가 복원효율이 가장 높은 것으로 평가되었다.

• 구강회복응용과학지
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• 제22권1호
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• pp.101-110
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• 2006

This study was performed to investigate the surface properties and in vitro biocompatibility of electrochemically oxidized Ti-6Al-7Nb alloy by anodic spark discharge technique. Discs of Ti-6Al-7Nb alloy of 20 mm in diameter and 2 mm in thickness were polished sequentially from #300 to 1000 SiC paper, ultrasonically washed with acetone and distilled water for 5 min, and dried in an oven at $50^{\circ}C$ for 24 hours. Anodizing was performed using a regulated DC power supply. The applied voltages were given at 240, 280, 320, and 360 V and current density of $30mA/cm^2$. Hydrothermal treatment was conducted by high pressure steam at $300^{\circ}C$ for 2 hours using a autoclave. Samples were soaked in the Hanks' solution with pH 7.4 at $36.5^{\circ}C$ during 30 days. The results obtained were summarized as follows; 1. The oxide films were porous with pore size of $1{\sim}5{\mu}m$. The size of micropores increased with increasing the spark forming voltage. 2. The main crystal structure of the anodic oxide film was anatase type as analyzed with thin-film X-ray diffractometery. 3. Needle-like hydroxyapatie (HA) crystals were observed on anodic oxide films after hydrothermal treatment at $300^{\circ}C$ for 2 hours. The precipitation of HA crystals was accelerated with increasing the spark forming voltage. 4. The precipitation of the fine asperity-like HA crystals were observed after being immersed in Hanks' solution at $37^{\circ}C$. The precipitation of HA crystals was accelerated with increasing the spark forming voltage and the time of immersion in Hanks' solution. 5. The Ca/P ration of the precipitated HA layer was equivalent to that of HA crystal as increasing the spark forming voltage and the time of immersion in Hanks' solution.

• 한국전기전자재료학회논문지
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• 제14권4호
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• pp.309-315
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• 2001

Crystallized $LiMn_{2-y}Mg_{y}O_4$ powder was prepared by calcing the mixture of LiOH.$H_2O$, $MnO_2$ and MgO at $800^{\circ}C$ for 36h in an air atmosphere. The structure of $LiMn_{2-y}Mg_{y}O_4$ crystallites was analyzed from powder X-ray diffraction data as a cubic spinel, space group Fd3m. Though all cathode material showed spinel phase based on cubic phase in X-ray diffraction, other peaks gradually exhibited and became intense with increasing y value in $LiMn_{2-y}Mg_{y}O_4$. However, ununiform which calculated by (111) face and (222) face was constant in spite of the increase of y value, except pure $LiMn_2O_4$. AC impedance of Li/$LiMn_{2-y}Mg_{y}O_4$ cells revealed the similar resistance of about $70\Omega$ before cycling. In addition, The impedance of Li/$LiMn_{1.9}Mg_{0.1}O_4$ cell changed during charge and discharge or after cycling.

• Carbon letters
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• 제16권2호
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• pp.78-85
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• 2015

Activated carbons (ACs) were prepared by activation of coal tar pitch (CTP) in the range of $700^{\circ}C-1000^{\circ}C$ for 1-4 h using potassium hydroxide (KOH) powder as the activation agent. The optimal activation conditions were determined to be a CTP/KOH ratio of 1:4, activation temperature of $900^{\circ}C$, and activation time of 3 h. The obtained ACs showed increased pore size distribution in the range of 1 to 2 nm and the highest specific capacitance of 122 F/g in a two-electrode system with an organic electrolyte, as measured by a charge-discharge method in the voltage range of 0-2.7 V. In order to improve the performance of the electric double-layer capacitor electrode, various mixtures of CTP and petroleum pitch (PP) were activated at the optimal activation conditions previously determined for CTP. Although the specific capacitance of AC electrodes prepared from CTP only and the mixtures of CTP and PP was not significantly different at a current density of 1 A/g, the AC electrodes from CTP and PP mixtures showed outstanding specific capacitance at higher current rates. In particular, CTP-PP61 (6:1 mixture) had the highest specific capacitance of 132 F/g, and the specific capacitance remained above 90% at a high current density of 3 A/g. It was found that the high specific capacitance could be attributed to the increased micro-pore volume of ACs with pore sizes from 1 to 2 nm, and the high power density could be attributed to the increased meso-pore volume.