• Journal of Welding and Joining
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• 제22권2호
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• pp.78-84
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• 2004

Effects of manganese and carbon on the HAZ microstructural evolution in 500㎫ grade titanium oxide steels were investigated. Microstructural evolution primarily depends on supercooling. When cooled at 3$^{\circ}C$/s in 0.15%C-1.5%Mn steel, grain boundary and Widmanst tten ferrite formed at 640 and 62$0^{\circ}C$, respectively, followed by competitive formation of acicular ferrite and upper bainite inside of grain at 58$0^{\circ}C$. With an increase of manganese, degree of supercooling increased while critical cooling rate for the formation of gain boundary ferrite decreased. Consequently, the amount of acicular ferrite in HAZ was decreased in 2.0%Mn after initial increase in 1.0 and 1.5%Mn. Therefore, optimum supercooling should be maintained to accelerate acicular ferrite formation in titanium oxide steels. Low carbon steel, 0.11%C-1.5%Mn, showed larger amount of acicular ferrite than higher carbon steel because of effectiveness of diffusionless transformation in low carbon steel.

• 한국지반환경공학회 논문집
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• 제11권11호
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• pp.63-75
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• 2010

중금속으로 오염된 부지는 다양한 공법으로 복원이 가능하나 오염부지가 비교적 넓은 경우 중금속을 부지로부터 제거하는 적극적 공법은 기술적 어려움과 비용의 문제로 쉽게 사용할 수 없다. 그러므로 토양에서 중금속의 용출을 차단 및 지연하는 안정화 공법이 보다 현실적이라 할 수 있다. 본 연구에서는 국내의 비교적 큰 규모의 중금속 오염토양인 제련소 오염토양을 대상으로 magnetite, hematite, zeolite-A, zeolite-X, zeolite-Y, zinc oxide, calcium oxide, carbon trioxide, manganese oxide, manganese dioxide, fish bone, sodium phosphate 등의 다양한 안정화제의 적용성실험을 수행하였다. 비소, 납, 구리, 니켈, 아연 등의 다중 중금속으로 오염된 토양의 경우 1종의 안정화제로 안정화가 어려우며 기존 연구에서 보고된 특정 중금속의 안정화에 우수한 성능을 갖는 안정화제의 경우에도 다른 중금속의 안정화에 기여하지 못하거나 용출을 촉진하는 경향을 보였다. 시간이 경과함에 따라 안정화 효율이 증가하였다. 니켈과 납의 경우 calcium oxide, carbon trioxide, manganese oxide 등의 안정화제가 효과가 있으며 특히 연속추출에서 물에 의한 추출부분에서 안정화 효율이 높았다. 구리의 경우 manganese oxide, zeolite 등이 효과가 크며 연속추출에서 exchangeable 추출부분에서 안정화 효율이 높았다. 비소의 경우 magnetite에 의한 안정화 효과를 보이며 대부분의 metal oxide와 phosphate 에 의해 용출이 촉진되는 부작용을 보였다. 그러므로 다양한 중금속으로 오염된 토양의 경우 2종 이상의 안정화제를 사용하여야 하며 역효과를 일으키는 안정화제의 사용을 배제하고 중금속의 농도에 따라 사용량 및 안정화 기간을 달리하여야 할 것으로 판단된다.

• 한국표면공학회지
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• 제52권3호
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• pp.150-155
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• 2019

The carbon electrode was modified through manganese-catalyzed hydrogenation method for high energy density vanadium redox flow battery (VRFB). During the catalytic hydrogenation, the manganese oxide deposited at the surface of the carbon electrode stimulated the conversion reaction from carbon to methane gas. This reaction causes the penetration of the manganese and excavates a number of cavities at electrode surface, which increases the electrochemical activity by inducing additional electrochemically active site. The formation of the porous surface was confirmed by the scanning electron microscopy (SEM) images. Finally, the electrochemical performance test of the electrode with the porous surface showed lower polarization and high reversibility in the cathodic reaction compared to the conventional electrode.

• 상하수도학회지
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• 제20권6호
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• pp.813-822
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• 2006

Soluble manganese removal was analyzed as a function of filter media, filter depth, presence or absence of chlorination, and surface manganese oxide concentration in water treatment processes. Sand, manganese oxide coated sand (MOCS), sand+MOCS, and granular activated carbon(GAC) were used as filter media. Manganese removal, surface manganese oxide concentration, turbidity removal, and regeneration of MOCS in various filter media were investigated. Results indicated that soluble manganese removal in MOCS was rapid and efficient, and most of the removal happened at the top of the filter. When filter influent (residual chlorine 1.0mg/L) with an average manganese concentration of 0.204mg/L was fed through a filter column, the sand+MOCS and MOCS columns can remove 98.9% and 99.2% of manganese respectively on an annual basis. On the other hand, manganese removal in sand and the GAC column was minimal during the initial stage of filtration, but after 8 months of filter run they removed 99% and 35% of manganese, respectively. Sand turned into MOCS after a certain period of filtration, while GAC did not. In MOCS, the manganese adsorption rate on the filter media was inversely proportional to the filter depth, while the density of media was proportional to the filter depth.

• 전기화학회지
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• 제15권3호
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• pp.198-205
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• 2012

리튬-공기전지 공기극으로서 탄소 상에 직접 수열합성법으로 망간산화물을 생성한 탄소지지 망간산화물 촉매를 합성하였다. 각 수열합성 조건에 따라서 만들어진 복합체에 대한 XRD, FE-SEM 분석을 통하여, 복합체의 결정구조, 형태, 크기 등을 확인하였는데 특히, 수열합성 온도 및 시간이 각각 $170^{\circ}C$, 12시간인 조건에서 만들어진 산화망간은 길이가 40-50 nm인 막대 모양을 갖는 것으로 나타났다. 합성된 복합체를 사용하여 만든 공기극과 리튬금속을 음극으로 하는 코인셀 형태의 리튬-공기전지를 만들어 전기화학적 특성을 조사한 결과 초기 방전 용량이 3,852 mAh/g으로 높았고 충 방전 횟수가 4회 정도 발현되었다.

• 한국표면공학회지
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• 제49권4호
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• pp.357-362
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• 2016

In this study, we manufactured the anodized alumina oxide (AAO) template and fabricated the carbon nanofibers and manganese oxide nanofibers using AAO template for application to electrochemical capacitor. Pore diameters of the AAO template were increased from 50 to 90 nm by increasing the acid treatment time after two-step anodizing process. Furthermore nanofibers, which is fabricated by AAO template, showed uniform diameter and micro structure. It is suggested that the surface area is larger than commercial electrode material and it is enhancing the energy density by increasing the specific capacitance.

• 한국응용과학기술학회지
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• 제17권1호
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• pp.49-53
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• 2000

For decompose carbon dioxide, manganese oxide was synthesized with $0.25M-MnSO_{4}{\cdot}nH_{2}O$ and 0.5M-NaOH by coprecipitation. We made magnetite deoxidized manganese oxide by hydrogen reduction for 1hour at $330^{\circ}C$. We investigated characteristics of catalyst, hydrogen reduction degree and decomposition rate of carbon dioxide. The structure of the hausmannite certified spinel type. The specific surface area of synthesized hausmannite and deoxidized hausmannite were $22.36m^{2}/g$, $33.56m^{2}/g$ respectively. The decomposition rate of $CO_{2}$ of deoxidized hausmannite was 57%.

• 대한전자공학회:학술대회논문집
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• 대한전자공학회 2001년도 The 6th International Symposium of East Asian Resources Recycling Technology
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• pp.409-412
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• 2001

The high purity manganese oxides were made from the dust, generated in AOD process that produces a medium-low carbon ferromanganese and collected in the bag filter. Manganese oxide content in the dust was about 90%, and its phase was confirmed as Mn₃O₄. In the extraction of manganese, because of remaining amorphous MnO₂, the dust was reduced to MnO by roasting with charcoal. The pulp density of the reduced dust can control pH of the solution more than 4 and then Fe ion is precipitated to a ferric hydroxide. Because a ferric hydroxide co precipitates with Si ion etc, Fe, Si ion was removed f개m the solution. Heating made water to be volatized and nitrates was left in reactor Then nitrates were a liquid state and stirring was possible. Among the nitrates in reactor, only the manganese nitrate which have the lowest pyrolysis temperature pyrolyzed into β-MnO₂powder and NO₂(g) at the temperature less than 200℃. When the pyrolysis of manganese nitrate has been completed about 90%, injection of water stopped the pyrolysis. Nitrates of impurity dissolved and the spherical high purity β-MnO₂powders were obtained by filtering and washing. Mn₂O₃or Mn₃O₄ powder could be manufactured from β-MnO₂powder by controlling the heating temperature. Lastly, a manufactured manganese oxide particle has 99.97% purity.

• 한국신재생에너지학회:학술대회논문집
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• 한국신재생에너지학회 2007년도 추계학술대회 논문집
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• pp.143-146
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• 2007

Birnessite-type manganese dioxide($MnO_2$) was coated uniformly onto carbon nanotubes (CNTs) through a spontaneous direct redox reaction between CNTs and permanganate ions($MnO_4\;^-$). The initial specific capacitance of the $MnO_2/CNT$ nanocomposite in an organic electrolyte at a large current density of 1 A/g was 250 F/g, which is equivalent to 139 mAh/g based on the total weight of the electrode material including the electroactive material, conducting agent and binder. The specific capacitance of the $MnO_2$ in the $MnO_2/CNT$ nanocomposite was as high as 580 F/g (320 mAh/g), indicating excellent electrochemical utilization of the $MnO_2$. The addition of CNTs as a conducting agent can improve the high rate capability of $MnO_2/CNT$ nanocomposite considerably. An analysis of the in-situ X-ray absorption near-edge structure (XANES) showed an improvement in the structural and electrochemical reversibility of the $MnO_2/CNT$ nanocomposite by heat-treatment.

• 한국응용과학기술학회지
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• 제32권1호
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• pp.23-30
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• 2015

The properties of dust collected from electric arc furnace of ferro manganese production units was investigated, and also the metallic manganese was recovered from the dust by aluminothermy process. The ferromanganese dust collected from electric arc furnace contained about 15% of manganese oxide ($Mn_3O_4$) and 9% of carbon as the contaminant, and have a 5um of 50% median diameter and irregular particle shape. The carbon contaminant in the dust could be reduced until about 0.1~0.5% level by roasting in the air at a temperature of 600~900C for 60minutes. The recovery of manganese could not be carried out using only ferromanganese dust from electric arc furnace by aluminothermy process, but the ferromanganese which contained manganese of about 92% and iron of about 5% could be obtained from the mixture of ferromanganese dusts from electric arc furnace and converter. The best mixing condition of dust fixed at electric arc furnace dust / converter dust ratio of 1:9 and 2:8, and the mixing rato of 3:7 or more could not separated the metal and slag from the reactant after aluminothermy reaction.