• 제목/요약/키워드: Mn concentration

검색결과 1,095건 처리시간 0.03초

열분해 방식에 따른 고체 커패시터의 특성연구 (A Study on the Characteristics of Solid Capacitor According to the Pyrolysis Methods)

  • 김재근;유형진;홍웅희
    • Korean Chemical Engineering Research
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    • 제44권6호
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    • pp.614-622
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    • 2006
  • 질산망간수용액의 열분해에 의한 이산화망간 적용 $Ta/Ta_2O_5/MnO_2$ 커패시터의 특성 연구를 수행하였다. 질산망간수용액의 TG/DSC 분석을 통해 약 $230{\sim}250^{\circ}C$ 범위에서 단일상의 이산화망간이 생성되었다. 열분해 온도, 질산망간수용액의 농도, 열분해 회수를 이산화망간 고체 전해질 생성의 기초 변수로 선정하고 이에 따른 커패시터 특성을 평가하였다. 최적 조성을 기준으로 복사열분해 방식이 대류열분해 방식에 비하여 우수한 특성을 발휘하였다. 이는 복사열분해에 의해 상대적으로 구형의 작은 입자 상태의 이산화망간 입자들이 생성되고 이를 통해 미세 다공성 구조의 커패시터 소결체 내부에 균일하고 치밀한 이산화망간 고체전해질 층이 생성되는 것에서 기인하는 결과임을 확인하였다.

저온에서 Mn-Cu 촉매의 NOx 전환특성 (NOx Conversion of Mn-Cu Catalyst at the Low Temperature Condition)

  • 박광희;유승한;박영옥;김상웅;차왕석
    • 한국산학기술학회논문지
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    • 제12권9호
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    • pp.4250-4256
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    • 2011
  • 활성증진 물질 Cu가 첨가된 Mn계 촉매를 제조하여 암모니아를 이용하여 질소산화물을 제거하는 SCR공정에서 질소산화물제거능을 측정하였다. 제조된 촉매를 사용하여 반응온도, 유량, 수분함량 그리고 산소농도에 대한 활성변화를 조사하였다. $H_2$-TPR 시스템에서 온도에 따른 촉매의 수소전환특성을 측정하였다. 수분공급유무를 조절함으로써 촉매반응에 대한 수분의 억제효과를 파악하였다. Mn-Cu계 촉매는 $160{\sim}260^{\circ}C$의 온도범위에서 높은 탈질효율을 보였다. 그리고 산소농도의 증가는 촉매활성 증진효과를 가져왔으나 수분함유는 촉매활성을 감소시키는 역할을 함을 알 수 있었다.

과망간산칼륨을 이용한 용해성 망간 제거: 중탄산염 영향 및 최적조건 (Manganese removal by KMnO4: Effects of bicarbonate and the optimum conditions)

  • 이용수;도시현;권영은;홍성호
    • 상하수도학회지
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    • 제30권2호
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    • pp.207-213
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    • 2016
  • This study is focused on manganese (Mn(II)) removal by potassium permanganate ($KMnO_4$) in surface water. The effects of bicarbonate on Mn(II) indicated that bicarbonate could remove Mn(II), but it was not effectively. When 0.5 mg/L of Mn(II) was dissolved in tap water, the addition of $KMnO_4$ as much as $KMnO_4$ to Mn(II) ratio is 0.67 satisfied the drinking water regulation for Mn (i.e. 0.05 mg/L), and the main mechanism was oxidation. On the other hand, when the same Mn(II) concentration was dissolved in surface water, the addition of $KMnO_4$, which was the molar ratio of $KMnO_4/Mn(II)$ ranged 0.67 to 0.84 was needed for the regulation satisfaction, and the dominant mechanisms were both oxidation and adsorption. Unlike Mn(II) in tap water, the increasing the reaction time increased Mn(II) removal when $KMnO_4$ was overdosed. Finally, the optimum conditions for the removals of 0.5 - 2.0 mg/L Mn(II) in surface water were both $KMnO_4$ to Mn(II) ratio is 0.67 - 0.84 and the reaction time of 15 min. This indicated that the addition of $KMnO_4$ was the one of convenient and effective methods to remove Mn(II).

철에 의한 버네사이트의 결정도 및 화학적 활성의 변화 (Crystallinity and Chemical Reactivity of Bimessite(δ-MnO2) Influenced by Iron)

  • 김재곤
    • 한국토양비료학회지
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    • 제32권4호
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    • pp.327-332
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    • 1999
  • 산화망간이 영양소물질과 오염물질과의 반응 및 망간이 식물의 필수 미량원소 등으로 인해 토양학에서 산화망간은 중요한 연구의 대상이 되어왔다. 토양 내에서 가장 흔한 산화망간 광물중의 하나인 버네사이트를 철의 존재 하에서 합성하였다. 토양 내에서 흔한 원소의 하나인 철이 버네사이트의 결정도, 형태 및 화학적 활성에 미치는 영향을 X-선회절, 전지현미경, 양이온 교환능력 및 크롬 산화력을 이용하여 연구하였다. 침전용액내의 철의 함량이 증가할수록 버네사이트의 결정도와 입자의 크기는 감소하였다. 침전된 버네사이트는 낮은 철의 농도에서 육각 판상형이 우세하였으나 농도가 증가 할 수록 미세입자로된 입단이 증가하였다. 그리고 크롬 산화능력은 철의 농도가 증가함에 따라 증가하였다. 양이온 치환능력은 철의 농도와 상관관계가 없었다. 침전용액속의 철은 버네사이트의 결정핵의 형성을 증가시켰고 표면흡착에 의해 결정의 성장을 방해하였다. 철은 토양 망간단과 내에서 산화철과 산화망간의 공존으로 미루어 보아 토양내의 버네사이트의 작은 입자, 낮은 결정도 및 높은 화학적 활성에 기여한 것으로 사료된다. 본 연구에서 입증된 버네사이트의 높은 양이온 교환 능력과 산화력은 버네사이트를 환경과 농업에 활용 가능성이 있음을 제시해준다.

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질산에 의한 중.저탄소페로망간제조분진에 함유된 망간의 침출 (The Extraction of Manganese from the Medium-Low Carbon Ferromanganese Dust with Nitric Acid)

  • 이계승;한기천;송영준;신강호;조동성
    • 자원리싸이클링
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    • 제9권1호
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    • pp.21-26
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    • 2000
  • 고탄소페로망간을 중.저탄소페로망간으로 제조하는 AOD공정의 Bag filter에 포집된 분진은 약 90%가 $Mn_3O_4$인 망간산화물이다. 분진의 입도는 5$\mu\textrm{m}$이하이고, 입자들은 직경이 10nm정도인 미립자들의 응집체로서 구형이다. 분진에서 망간을 질산으로 침출할 때의 최대침출율은 약 67%이며,비정질의 $MnO_2$가 잔류한다. 침출속도는 온도가 증가함에 따라 빨라지고 고농도의 질산에서는 늦어졌다. 침출속도를 여러 침출모델에 적용한 결과는 pore diffusion model에 일치하였다.

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High density plasma etching of CoFeB and IrMn magnetic films with Ti hard mask

  • Xiao, Y.B.;Kim, E.H.;Kong, S.M.;Chung, C.W.
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2009년도 제38회 동계학술대회 초록집
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    • pp.233-233
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    • 2010
  • Magnetic random access memory (MRAM), based on magnetic tunnel junction (MTJ) and CMOS, is a prominent candidate among prospective semiconductor memories because it can provide nonvolatility, fast access time, unlimited read/write endurance, low operating voltage and high storage density. The etching of MTJ stack with good properties is one of a key process for the realization of high density MRAM. In order to achieve high quality MTJ stack, the use of CoFeB and IrMn magnetic films as free layers was proposed. In this study, inductively coupled plasma reactive ion etching of CoFeB and IrMn thin films masked with Ti hard mask was investigated in a $Cl_2$/Ar gas mix. The etch rate of CoFeB and IrMn films were examined on varying $Cl_2$ gas concentration. As the $Cl_2$ gas increased, the etch rate monotonously decreased. The effective of etch parameters including coil rf power, dc-bais voltage, and gas pressure on the etch profile of CoFeB and IrMn thin film was explored, At high coil rf power, high dc-bais voltage, low gas pressure, the etching of CoFeB and IrMn displayed better etch profiles. Finally, the clean and vertical etch sidewall of CoFeB and IrMn free layers can be achieved by means of thin Ti hard mask in a $Cl_2$/Ar plasma at the optimized condition.

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A Separation of manganese (II) and cobalt (II) ions by D2EHPA/TBP-immobilized PolyHIPE membrane

  • Chen, Jyh-Herng;Mai, Le Thi Tuyet
    • Membrane and Water Treatment
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    • 제10권2호
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    • pp.127-137
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    • 2019
  • The D2EHPA/TBP co-extractants immobilized PolyHIPE membrane can be used for the selective separation of Mn (II) from Co (II). By solvent-nonsolvent method, D2EHPA/TBP co-extractants can be effectively immobilized into PolyHIPE membrane. The pore structure of PolyHIPE membrane and the presence of TBP enhance the stability of immobilized co-extractants. The optimal operating conditions for the separation of Mn (II) and Co (II) are feeding phase at pH 5.5, sulfuric acid concentration in the stripping phase of about 50 g/L and stirring speed at 400 rpm. The D2EHPA/TBP co-extractants ratio of 5:1 shows synergetic effect on Mn/Co separation factor about 22.74. The removal rate and recovery rate of Mn (II) is about 98.4 and 97.1%, respectively, while for Co (II) the transport efficiency is insignificant. The kinetic study of Mn (II) transport shows that high initial flux, $J_f^o=80.1({\mu}mol/m^2s)$, and maxima stripping flux, $J_s^{max}=20.8({\mu}mol/m^2s)$, can be achieved with D2EHPA/TBP co-extractants immobilized PolyHIPE membrane. The stability and reusability study shows that the membrane can maintain a long term performance with high efficiency. High purity of Co (II) and Mn (II) can be recovered from the feeding phase and stripping phase, respectively.

Trace elements analysis in some medicinal plants using graphite furnace-atomic absorption spectroscopy

  • Anal, Jasha Momo H.;Chase, Petevino
    • Environmental Engineering Research
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    • 제21권3호
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    • pp.247-255
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    • 2016
  • Ten trace elements (Mg, Ca, V, Cr, Mn, Fe, Cu, Zn, Mo, and Cd) were determined in seven traditionally used wild medicinal plants of the Nagas in the North-East India viz Cynoglossum furcatum Wallich, Elsholtzia blanda Bentham, Lycopodium cernuum Linnaeus, Potentilla fulgens Wallich ex Hooker, Swertia macrosperma C.B. Clarke, Thalictrum foliolosum DC and Valeriana jatamansi Jones. Plant samples were dried, weighed, digested and analyzed for their mineral distribution level ranging from trace to major elements by graphite furnace-atomic absorption spectroscopy. All the medicinal herbs studied were found to contain the ten elements analyzed. The elemental concentration is given in mg/kg. Mg and Ca are present in high concentrations in both the roots and leaves of the plant samples. Among trace transition metals Fe had the highest concentration, followed by Mn, Cr, Cu, V, Zn, and Mo. Analysis showed that the toxic Cd element was at a lower concentration and is within the permissible limit of FAO/WHO, California standards and United States Pharmacopeia Limit for Nutritional Supplements.

Mn-Zn 페라이트 다결정의 조성에 따른 투자율의 변화 기구 (Origin of the Initial Permeability of Manganese-Zinc Ferrite Polycrytals)

  • 변순천;제해준;고경현;홍국선
    • 한국세라믹학회지
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    • 제34권4호
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    • pp.351-356
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    • 1997
  • The origin of the variation of initial permeability in manganese-zinc ferrite polycrystals with a content of hematite was investigated. Initial permeability showed maximum with hematite content while there was no significant change in microstructure. Saturation magnetization increased with hematite content. So the variation of initial permeability was not explained on the basis of microstructural change or saturation magnetization. Temperature dependence of initial permeability revealed magnetocrystalline anisotropy was the origin of the variation of initial permeability. The change in magnetocrystalline anisotropy was ascribed to the variation in ferrous ion concentration. Therefore the variation of initial permeability in manganese-zinc ferrite polycrystals with a content of hematite was due to ferrous ion concentration via magnetocrystalline anisotropy.

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상업용 오존촉매와 광촉매를 이용한 오존제거특성 (Characteristics of Residual Ozone Decomposition with Commercial Ozone Decomposition Catalyst (ODC) and Photo catalyst)

  • 변정훈;박재홍;황정호
    • 대한기계학회:학술대회논문집
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    • 대한기계학회 2004년도 춘계학술대회
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    • pp.1255-1260
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    • 2004
  • Decomposition of ozone at room temperature was investigated comparatively with commercial monolithic ozone decomposition catalyst (ODC, $MnO_2$) and monolithic photo catalyst ($TiO_2$). The effects of residence time, UV (ultraviolet) light dependence and ozone concentration on the conversion was presented. UV ray was irradiated using BLB (black light blue) lamp ($315{\sim}400$ nm), supplied with a constant intensity in the reactor. The concentration of ozone in the square-shape reactor can be controlled by combining the DBD (dielectric barrier discharge) reactor with an AC high voltage supply system. The catalytic performance, in presence of UV irradiation did not show significant changes for $MnO_2$ catalyst. $TiO_2$ catalyst was the different case, which showed higher decomposition activity in presence of UV irradiation. Deactivation of catalyst detected by real-time ozone monitor for 120 hours with a constant inlet ozone concentration.

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