• 제목/요약/키워드: Dispersion of MgO

검색결과 62건 처리시간 0.027초

$(1-x)ZrO_2-xMgO$ 계의 미세입자 원료분말의 제조 (Fine Powder Preparation in the System of $(1-x)ZrO_2-xMgO$)

  • 안영필;김복희;성상현;정복환;이응상
    • 한국세라믹학회지
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    • 제22권5호
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    • pp.17-22
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    • 1985
  • This study was to make powder by coprecipitation method and spray dispersion precipitation method in $(1-x)ZrO_2-xMgO$ system to improve sinterability. As the result the specific surface area of powder prepared by spray dispersion precipitation method and coprecipitation method was above $110m^2/g$ and $10-20m^2/g$ respectively. Spray dispersion precipitation method was more effective than coprecipitation method in powder preparation.

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Platinum Nano-Dispersion via In Situ Processing - Preparation and catalytic Property of Porous $CaZrO_3/MgO/Pt$ Nanocomposite

  • Yoshikazu;Hwang, Hae-Jin;Naoki Kondo;Tatsuki Ohji
    • 한국분말재료학회지
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    • 제8권3호
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    • pp.163-167
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    • 2001
  • A bulk porous $CaZrO_3/MgO$ composite with plantinum nano-dispersion was synthesized in air atmosphere through the combination of several in situ reactions, including the pyrolysis of $PtO_2$. A mixture of $CaMg(CO_3)_2$(dolomite), $ZrO_2$, $PtO_2$ and LiF (0.5 wt%, as an additive) was cold isostatically pressed at 200 MPa and sintered at $1100^{\circ}C$ for 2 h. The porous $CaZrO_3/MgO/Pt$ composite ($CaZrO_3/MgO$ : Pt=99 : 1 in volume) had a uniformly open-porous structure (porosity: 56%) with three-dimensional (3-D) network and a narrow pore-size distribution, similarly to the porous $CaZrO_3/MgO$ composites reported before. Catalytic Properties (viz., NO direct decomposition and NO reduction by $C_2H_4$) of the $CaZrO_3/MgO/Pt$ composite were investigated up to $900^{\circ}C$. In the absence of oxygen, the NO conversion rate reached ~52% for the direct decomposition and ~100% for the reduction by $C_2H_4$, respectively. The results suggest the possibility of the porous composite as a multifunctional filter, i.e., simultaneous hot gas-filtering and $de-NO_x$ in one component.

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대현 금-은광상의 모암변질에 따른 원소분산 (Element Dispersion by the Wallrock Alteration of Daehyun Gold-silver Deposit)

  • 유봉철
    • 자원환경지질
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    • 제46권2호
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    • pp.199-206
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    • 2013
  • 대현 금-은광상은 Cambro-Ordovician 석회암질 대리암내에 발달된 NE 방향성의 단열대를 따라 형성된 2개의 열수성 석영맥으로 구성된다. 모암변질시 원소 분산과 이득/손실을 알아보기 위해 모암, 열수변질대 및 금-은 광맥에서 시료를 채취하였다. 모암변질시 뚜렷한 변질대가 관찰되지 않으며 구성광물은 주로 방해석, 돌로마이트, 석영과 소량 녹염석 등이다. 이 광상의 광석광물은 유비철석, 자류철석, 황철석, 섬아연석, 황석석, 황동석, 방연석, 에렉트럼, 자연 창연 및 은 광물 등이 산출된다. 분석된 자료를 기초로, 모암은 주로 $SiO_2$, CaO 및 $CO_2$로 구성되며 소량 $Al_2O_3$, $Fe_2O_3(T)$ 및 MgO 등이 함유되어 있다. 광체로부터 모암으로 감에 따라 $SiO_2$, $Fe_2O_3(T)$, MgO, CaO 및 $CO_2$ 함량은 변화 폭이 크게 관찰된다. 모암변질시 모암의 물리-화학적 물성 때문에 원소 분산은 현저히 관찰되지 않으며 단지 광체 주변부에서만 관찰된다. 모암변질시 이득원소들은 $Fe_2O_3(T)$, 총 S, Ag, As, Bi, Cd, Cu, Ni, Pb, Sb, Sn, W 및 Zn이고 손실원소들은 $SiO_2$, MnO, MgO, CaO. $CO_2$ 및 Sr 이다. 따라서 우리의 결과물은 황강리 광화대내 석회암질 대리암을 모암으로 갖는 광상들의 지화학탐사시 활용될 수 있을 것이다.

장군 연-아연-은 광상의 모암변질에 따른 원소분산 (Element Dispersion by the Wallrock Alteration of Janggun Lead-Zinc-Silver Deposit)

  • 유봉철
    • 자원환경지질
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    • 제45권6호
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    • pp.623-641
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    • 2012
  • 장군 연-아연-은 광상은 열수교대형 광상이다. 모암변질시 원소 분산을 알아보기 위해 모암, 열수변질대 및 연-아연-은 광맥에서 시료를 채취하였다. 이 광상은 능망간석화작용과 돌로마이트화작용으로 구성된 열수작용이 현저히 인지된다. 모암은 돌로마이트와 석회암이며 구성광물은 방해석, 돌로마이트, 석영, 금운모 및 흑운모 이다. 연-아연-은 광맥과 접촉한 부분에서 관찰되는 능망간석대는 주로 능망간석이 산출되며 소량 방해석, 돌로마이트, 쿠트나호라이트, 유비철석, 황철석, 황동석, 섬아연석, 방연석 및 황석석 등이 산출된다. 연-아연-은 광맥으로부터 멀어짐에 따라 관찰되는 돌로마이트대는 주로 돌로마이트가 산출되고 소량 방해석, 능망간석, 황철석, 섬아연석, 황동석, 방연석 및 황석석 등이 산출된다. 모암변질시 주원소, 미량 및 희토류원소들간의 상관계수는 $Fe_2O_3(T)$/MnO, Ga/MnO 및 Rb/MnO(돌로마이트 및 석회암)가 정의 상관관계를 갖고 MgO/MnO, CaO/MnO, $CO_2$/MnO 및 Sr/MnO(돌로마이트)와 CaO/MnO 및 Sr/MnO(석회암)가 부의 상관관계를 갖는다. 모암변질시 이득원소들은 $Fe_2O_3(T)$, MnO, As, Au, Cd, Cu, Ga, Pb, Rb, Sb, Sc, Sn 및 Zn 이고 손실원소들은 CaO, MgO, $CO_2$ 및 Sr 이다. 따라서 CaO, $CO_2$, $Fe_2O_3(T)$, MgO, MnO, Ga, Pb, Rb, Sb, Sn, Sr 및 Zn 등의 원소들은 모암이 돌로마이트내지 석회암인 열수교대형 광상의 탐사에 지시원소로서 활용될 수 있을 것이다.

Electrical Insulation Properties of Nanocomposites with SiO2 and MgO Filler

  • Jeong, In-Bum;Kim, Joung-Sik;Lee, Jong-Yong;Hong, Jin-Woong;Shin, Jong-Yeol
    • Transactions on Electrical and Electronic Materials
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    • 제11권6호
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    • pp.261-265
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    • 2010
  • In this paper, we attempt to improve the electrical characteristics of epoxy resin at high temperature (above $80^{\circ}C$) by adding magnesium oxide (MgO), which has high thermal conductivity. Scanning electron microscopy (SEM) of the dispersion of specimens with added MgO reveals that they are evenly dispersed without concentration. The dielectric breakdown characteristics of $SiO_2$ and MgO nanocomposites are tested by measurements at different temperatures to investigate the filler's effect on the dielectric breakdown characteristics. The dielectric breakdown strength of specimens with added $SiO_2$ decreases slowly below $80^{\circ}C$ (low temperature) but decreases rapidly above $80^{\circ}C$ (high temperature). However, the gradient of the dielectric breakdown strength of specimens with added MgO is slow at both low and high temperatures. The dielectric breakdown strength of specimens with 0.4 wt% $SiO_2$ is the best among the specimens with added $SiO_2$, and that of specimens with 3.0 wt% and 5.0 wt% MgO is the best among those with added MgO. Moreover, the dielectric strength of specimens with 3.0 wt% MgO at high temperatures is approximately 53.3% higher than that of specimens with added $SiO_2$ at $100^{\circ}C$, and that of specimens with 5.0 wt% of MgO is approximately 59.34% higher under the same conditions. The dielectric strength of MgO is believed to be superior to that of $SiO_2$ owing to enhanced thermal radiation because the thermal conductivity rate of MgO (approximately 42 $W/m{\cdot}K$) is approximately 32 times higher than that of $SiO_2$ (approximately 1.3 $W/m{\cdot}K$). We also confirmed that the allowable breakdown strength of specimens with added MgO at $100^{\circ}C$ is within the error range when the breakdown probability of all specimens is 40%. A breakdown probability of up to 40% represents a stable dielectric strength in machinery and apparatus design.

Selective Oxidation of Hydrogen Sulfide to Elemental Sulfur with Fe/MgO Catalysts in a Slurry Reactor

  • Lee, Eun-Ku;Jung, Kwang-Deog;Joo, Oh-Shim;Shul, Yong-Gun
    • Bulletin of the Korean Chemical Society
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    • 제26권2호
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    • pp.281-284
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    • 2005
  • The Fe/MgO catalysts with different Fe loadings (1, 4, 6, 15 and 30 wt% Fe) were prepared by a wet impregnation with iron nitrate as precursor. All of the catalysts were characterized by BET surface analyzer, X-ray diffraction (XRD), temperature-programmed reduction (TPR), and X-ray photoelectron spectroscopy (XPS). The maximum removal capacity of $H_2S$ was obtained with 15 wt% Fe/MgO catalyst which had the highest BET surface area among the measured catalysts. XRD of Fe/MgO catalysts showed that well dispersed Fe particles could be present on Fe/MgO with Fe loadings below 15 wt%. The crystallites of bulk $\alpha$-$Fe_2O_3$ became evident on 30 wt% Fe/MgO, which were confirmed by XRD. TPR profiles showed that the reducibility of Fe/MgO was strongly related to the loaded amounts of Fe on MgO support. Therefore, the highest removal efficiency of $H_2S$ in wet oxidation could be ascribed to a good dispersion and high reducibility of Fe/MgO catalyst. XPS studies indicated that the $H_2S$ oxidation with Fe/MgO could proceed via the redox mechanism ($Fe^{3+}\;{\leftrightarrow}\;Fe^{2+}$).

MgO를 첨가한 에폭시 나노 컴퍼지트의 절연파괴강도 온도의존성 (Temperature Dependence on dielectric breakdown strength of Epoxy Nano-Composites depending on MgO)

  • 정인범;한현석;이영상;조경순;신종열;홍진웅
    • 한국전기전자재료학회:학술대회논문집
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    • 한국전기전자재료학회 2010년도 하계학술대회 논문집
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    • pp.48-48
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    • 2010
  • In this paper, we have investigated temperature dependence of dielectric breakdown voltage at epoxy with added nano-filler(MgO), which is used as a filler of epoxy additives for HVDC(high voltage direct current) submarine cable insulating material with high thermal conductivity and restraining tree to improve electrical properties of epoxy resin in high temperature region. In order to find dispersion of the specimen, the cross sectional area of nano-composite material is observed by using the SEM(Scanning Electron Microscope) and it is conformed that each specimen is evenly distributed without the cohesion. As a result, it is confirmed that the strength of breakdown of all specimen at 50 [$^{\circ}C$] decreased more than that of the dielectric breakdown strength at room temperature. When temperature increases from 50 [$^{\circ}C$] to 100 [$^{\circ}C$], we have confirmed that breakdown strength of virgin specimen decreases, but specimens with added MgO show constant dielectric breakdown strength.

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Al-Si/SiCp 복합조직에 미치는 Rheo-compocasting의 제조조건 및 Mg첨가의 영향 (Influence of Rheo-compocasting Conditions and Mg Additions on the Microstructures in Al-Si/SiCp Composite)

  • 김석원;이의권;전우용
    • 한국주조공학회지
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    • 제13권6호
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    • pp.524-531
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    • 1993
  • Dispersion behaviors of SiC particles and microstructures in Al-2%Si/SiCp composite prepared by Rheo-compocasting were studied with change of fabrication conditions(slurry temperature, agitation time) and additions of Mg($0{\sim}3wt.%$). Also, the microhardness change of matrix, interface and total in composites were examined with additions of Mg($0{\sim}3wt.%$). The dispersion of particles in the composites became relatively homogeneous with increase of Mg additions, agitation time and decrease of slurry temperature. Rate of occupied area by particle in matrix was increased as increase of Mg additions due to improvement of wettability between SiC particle and matrix. A favorable composites were obtained by melting under Ar atmospheric SiCp injection and bottom pouring system. According to the analysis of X-ray diffraction, $Mg_2Si$, $Al_4C_3$, $SiO_2$ and MgO, etc, intermetallic compounds were formed by chemical interreaction at interface of matrix and particles. The microhardness of interface is higher than that of matrix due to more strengthening of above intermetallic compounds. It was considered that the total hardness of the composites is improved by dispersing of SiCp and addition of Mg.

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Hydrogen Production from Methane Reforming Reactions over Ni/MgO Catalyst

  • ;노현석;;전기원;박상언
    • Bulletin of the Korean Chemical Society
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    • 제22권12호
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    • pp.1323-1327
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    • 2001
  • The catalyst Ni/MgO (Ni : 15 wt%) has been applied to methane reforming reactions, such as steam reforming of methane (SRM), partial oxidation of methane (POM), and oxy-steam reforming of methane (OSRM). It showed high activity and good stability in all the reforming reactions. Especially, it exhibited stable catalytic performance even in stoichiometric SRM (H2O/CH4 = 1). From TPR and H2 pulse chemisorption results, a strong interaction between NiO and MgO results in a high dispersion of Ni crystallite. Pulse reaction results revealed that both CH4 and O2 are activated on the surface of metallic Ni over the catalyst, and then surface carbon species react with adsorbed oxygen to produce CO.

밀양지역 납석광상 화산암질 모암에서의 원소들의 지구화학적 분산 (Geochemical Dispersion of Elements in Volcanic Wallrocks of Pyrophyllite Deposits in Milyang Area, Kyeongnam Province)

  • 오대균;전효택
    • 자원환경지질
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    • 제26권3호
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    • pp.337-347
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    • 1993
  • Mineralogical and geochemical studies on some pyrophyllite deposits in Milyang area, Kyeongnam Province (Milyang and Sungjin mine) were carried out in order to investigate dispersion patterns of chemical elements in altered volcanic wallrocks, and to interpret genetic environments of the pyrophyllite deposits. Cretaceous andesitic and tuffaceous rocks, and pyrophyllite ore specimens were collected from the dumps and drilling cores. Andesitic wallrocks were grouped as unaltered and altered rocks in the order of pyrophyllitization. Vertical dispersion patterns and relative mobilities of chemical elements in volcanic wallrocks were discussed. Geochemical environment in the Milyang area is characterized by the occurrence of boron minerals such as dumortierite coexisting with pyrophyllite ores, and tourmaline in granitic rocks. Unaltered andesitic rocks are mainly composed of plagioclase, pyroxene and hornblende, and were propylitized and saussuritized. Altered andesitic rocks are bleached and consist of quartz, sericite, pyrophyllite, kaolinite, chlorite and disseminated pyrite. Pyrophyllite ores are mainly composed of quartz, pyrophyllite, dumortierite, dissemianted pyrite and some diaspore. Enrichment of $SiO_2$, $Al_2O_3$, LOI (loss on ignition), As and Cr, and depletion of $K_2O$, $Na_2O$, CaO, MgO and total Fe are characteristic during alteration process. The REE patterns show that the pyrophyllite deposits could be originated from the continental margin volcanics. The $(La/Lu)_{cn}$ ratios of the pyrophyllite ores increase from 4.2~23.2 to 2.67~128.8 owing to strong acidic hydrothermal alteration. Vertical dispersion patterns of $Al_2O_3$, $K_2O$, $Na_2O$, CaO, MgO, $Fe_2O_3$ (total Fe), As, Au, Sb, Cr and Sr in the wallrocks show the location of orebodies. Particularly dispersion patterns of $Al_2O_3$ and Cr indicate the extension of orebodies. Anomalous distribution of Au, As and Sb in wallrocks shows potential for gold occurrence below the pyrophyllite deposits. Judging from the relative mobilities of elements in wallrocks, $Al_2O_3$ could be added from hydrothermal solution, and the silicified rone be formed from the excess of $SiO_2$.

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