• 제목/요약/키워드: Nano-Sized Particles

검색결과 361건 처리시간 0.038초

EPD를 이용한 IT-SOFC용 SDC 전해질 필름의 제조 (Preparation of SDC electrolyte film for IT-SOFCs by electrophoretic deposition)

  • 이경섭;김영순;조철기;신형식
    • 한국신재생에너지학회:학술대회논문집
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    • 한국신재생에너지학회 2009년도 추계학술대회 논문집
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    • pp.158-158
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    • 2009
  • The electrophoretic deposition(EPD) technique with a wide range of novel applications in the processing of advanced ceramic materials and coatings, has recently gained increasing interest both in academic and industrial sector not only because of the high versatility of its use with different materials and their combinations but also because of its cost-effectiveness requiring simple apparatus. Compared to other advanced shaping techniques, the EPD process is very versatile since it can be modified easily for a specific application. For example, deposition can be made on flat, cylinderical or any other shaped substrate with only minor charge in electrode design and positioning[1]. The synthesis of the nano-sized Ce0.2Sm0.8O1.9(SDC)particles prepared by aurea based low temperature hydrothermal process was investigated in this study[2].When we made the SDC nanoparticles, changed the time of synthesis of the SDC. The SDC nanoparticles were characterized with field-emission scanning electron microscope(FESEM), energy dispersive X-ray analysis(EDX), and X-ray diffraction(XRD). And also we researched the results of our investigation on electrophoretic deposition(EPD) of the SDC particles from its suspension in acetone solution onto a non-conducting NiO-SDC substrate. In principle, it is possible to carry out electrophoretic deposition on non-conducting substrates. In this case, the EPD of SDC particles on a NiO-SDC substrate was made possible through the use of a adequately porous substrate. The continuous pores in the substrates, when saturated with the solvent, helped in establishing a "conductive path" between the electrode and the particles in suspension[3-4]. Deposition rate was found to increase its increasing deposition time and voltage. After annealing the samples $1400^{\circ}C$, we observed that deposited substrate.

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Chemical mechanical planarization 슬러리에 사용되는 point-of-use 필터의 평가 방법 개발 (Development of point-of-use filter evaluation method using chemical mechanical planarization slurry)

  • 장선재;아툴 쿨르카르니;김형우;김태성
    • 한국입자에어로졸학회지
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    • 제12권4호
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    • pp.145-150
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    • 2016
  • During the chemical mechanical planarization (CMP) process, slurry that comprises abrasive particles can directly affect the CMP performance and quality. Mainly, the large particles in the slurry can generate the defects on the wafer. Thus, many kinds of filters have been used in the CMP process to remove unwanted over-sized particles. Among these filters, the point-of-use (POU) filter is used just before the slurry is supplied onto the CMP pad. In the CMP research field, analysis of the POU filter has been relatively exceptional, and previous studies have not focused on the standardized filtration efficiency (FE) or filter performance. Furthermore, conventional evaluation methods of filter performance are not appropriate for POU filters, as the POU filter is not a membrane type, but is instead a depth type roll filter. In order to accurately evaluate the POU filter, slurry FE according to particle size was measured in this study. Additionally, a CMP experiment was conducted with filtered slurry to demonstrate the effects of filtered slurry on CMP performance. Depending on the flow rate and the filter retention size, the FE according to particle size was different. When the small and large particles have different FEs, the total filtration efficiency (TFE) can still have a similar value. For this reason, there is a need to measure the FE with respect to the particle size to verify the effects of the POU filter on the CMP process.

α-Fe2O3 나노 입자에서 Spin-Flop에 관한 연구 (Spin-Flop of α-Fe2O3 Nano Particles)

  • 서정철;박철진;최정완
    • 한국자기학회지
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    • 제14권5호
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    • pp.169-173
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    • 2004
  • $\alpha$-F $e_2$ $O_3$, 나노 입자를 균일한 크기로 제조하여 Morin 전이 온도( $T_{M}$)를 전 후로 스핀의 변화에 관하여 연구하였다. X-선 회절 분석과 입도분포 측정을 통하여 입자는 80nm정도의 매우 군일한 크기 분포를 하고 있음을 확인하였다. Mossbauer 분광기를 통하여 4.2K에서부터 실내온도까지 여러 온도 범위에 걸쳐 측정한 결과 입자의 크기에 따라 $T_{M}$온도가 변화되었고 스핀의 상태 역시 달라졌다. $T_{M}$$b_{ulk}$상태에서 265 K의 값을 가지고 있으나 입자의 크기가 작아질수록 낮아지고, 임계 크기 이하에서는 전이가 전혀 일어나지 않는다. 80nm크기의 입자에서, 스핀의 방향은 $T_{M}$ 이상의 온도에서는 정상적으로 hexagonal구조의 c축에 90$^{\circ}$ 이루고 있으나 $T_{M}$ 이하의 온도에서는 c 축에 나란하지 않고 일정한 각(28$^{\circ}$~29$^{\circ}$)을 유지하는데, 이 방향은 rhombohedral구조의 [110]에 해당하는 것으로 지금까지 알려진 0$^{\circ}$와 90$^{\circ}$사이의 스핀 전이와는 다른 모습을 보여주고 있다.

산화철 나노입자 표면개질 분말활성탄 유동층에 의한 MF 막 분리 공정의 운전 및 NOM 제거 효율 향상 (Effect of Fluidized Bed Powdered Activated Carbon Impregnated by Iron Oxide Nano-particles on Enhanced Operation and NOM Removal of MF Membrane System)

  • 김성수;서규태
    • 대한환경공학회지
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    • 제33권5호
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    • pp.332-339
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    • 2011
  • 본 연구는 자력분리와 중력분리의 특징을 가진 산화철 나노입자 표면개질 분말활성탄에 의한 MF막 분리 공정의 운전 및 NOM 제거 효율에 미치는 영향을 알아보았다. MF막의 전처리로 표면개질 PAC 유동층 칼럼을 구성하였으며, 표면개질 PAC층은 63 m/d의 유속에서 표면개질 PAC 입자가 유출되지 않은 최대의 유속을 유지하였고, 이 때 접촉시간은 29분이었다. 유동상칼럼 상단에는 경자성체(magnet)를 설치하여 부유하는 미세한 입자의 유출을 방지하였다. 직렬로 구성한 표면개질 PACMF 결합공정에서 표면개질 PAC 칼럼을 통하여 MF막의 파울링 저감과 NOM 제거효율의 상당한 향상을 보였다. MF막만을 이용하였을 때에 막 차압은 98시간 만에 적정운전범위인 40 kPa이 초과되었으나, 표면개질 PAC 칼럼을 함께 구성하였을 때 막 차압은 여전히 12 kPa의 안정적으로 유지되었다. NOM의 제거효율 또한 표면개질 PAC의 전처리를 통해서 DOC와 $UV_{254}$가 각각 46%와 51%에서 75%와 84%로 상승하였다. 시스템 내 NOM의 제거현상을 알아보기 위한 HPLC-SEC 분석을 통해서 표면개질 PAC는 광범위한 분자량을 가진 유기물의 효과적인 제거가 가능한 것을 알 수 있었다.

구형 Ni과 나노 YSZ Powder를 이용하여 제조한 Ni/YSZ Core-shell의 SOFC 연료극 특성 (Characteristics of SOFC Anode of Ni/YSZ Core-shell Manufactured Using sSpherical Ni and Nano YSZ Powders)

  • 최병현;구자빈;설광희;지미정
    • 한국수소및신에너지학회논문집
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    • 제28권1호
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    • pp.40-46
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    • 2017
  • We reviewed the electrical properties of SOFC anode manufactured using spherical Ni and nano YSZ powder. When core-shell is fabricated by using submicron Ni as core and nano-sized YSZ as shell for SOFC anode, the electrical conductivity of the $0.2{\mu}m$ Ni-YSZ core-shell was 3 times higher than that of $1.0{\mu}m$ NiO or $1.0{\mu}m$ Ni-YSZ. Hydrogen selectivity was similar at $800^{\circ}C$, but hydrogen selectivity and methane conversion rate under $750^{\circ}C$ was 10~25% higher, Power density was more than 2 times, ASR was about 1/3, when exposed to $H_2$ atmosphere at $750^{\circ}C$ for a long time, Ni particles did not have any growth or cut off conduction path.

Growth and Migration of BALB/3T3 Fibroblast Cells on Nano-engineered Silica Beads Surface

  • Kim, Jihee;Chandra, Prakash;Yang, Jiyoon;Rhee, Seog Woo
    • Bulletin of the Korean Chemical Society
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    • 제34권12호
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    • pp.3715-3721
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    • 2013
  • In this study, the behavior of cells on the modified surface, and the correlation between the modified substrates and the response of cells is described. A close-packed layer of nano-sized silica beads was prepared on a coverslip, and the adhesion, proliferation, and migration of BALB/3T3 fibroblast cells on the silica layer was monitered. The 550 nm silica beads were synthesized by the hydrolysis and condensation reaction of tetraethylorthosilicate in basic solution. The amine groups were introduced onto the surfaces of silica particles by treatment with 3-aminopropyltrimethoxysilane. The close-packed layer of silica beads on the coverslip was obtained by the reaction of the amine-functionalized silica beads and the (3-triethoxysilyl)propylsuccinic anhydride treated coverslip. BALB/3T3 fibroblast cells were loaded on bare glass, APTMS coated glass, and silica bead coated glass with the same initial cell density, and the migration and proliferation of cells on the substrates was investigated. The cells were fixed and stained with antibodies in order to analyze the changes in the actin filaments and nuclei after culture on the different surfaces. The motility of cells on the silica bead coated glass was greater than that of the cells cultured on the control substrate. The growth rate of cells on the silica bead coated glass was slower than that of the control. Because the close-packed layer of silica beads gave an embossed surface, the adhesion of cells was very weak compared to the smooth surfaces. These results indicate that the adhesion of cells on the substrates is very important, and the actin filaments might play key roles in the migration and proliferation of cells. The nuclei of the cells were shrunk on the weakly adhered surfaces, and the S1 stage in which DNA is duplicated in the cell dividing processes might be retarded. As a result, the rate of proliferation of cells was decreased compared to the smooth surface of the control. In conclusion, the results described here are very important in the understanding of the interaction between implanted materials and biosystems.

Effect of Ag on microstructural behaviour of Nanocrystalline $Fe_{87-x}Zr_7B_6Ag_x$($0{\leq}x_{Ag}{\leq}4$) Magnetic Thin Films Materials

  • 이원재;민복기;송재성
    • 한국전기전자재료학회:학술대회논문집
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    • 한국전기전자재료학회 2002년도 춘계학술대회 논문집 초전도 자성체
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    • pp.3-6
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    • 2002
  • Effect of Ag additive element on microstructure of $Fe_{87-x}Zr_7B_6Ag_x$, magnetic thin films on Si(001) substrates has been investigated using Transmission Electron Microscopy(TEM) and X-ray Diffraction(XRD). All samples with additive Ag element were made by DC-sputtering and subjected to annealing treatments of $300^{\circ}C{\siim}600^{\circ}C$ for 1 hr. TEM and XRD showed that perfectly amorphous state in Ag-free Fe-based films was observed in as-deposited condition. The as-deposited Fe-based films with the presence of Ag constituent have a mixture of Fe-based amorphous and nano-sized Ag crystalline phases. In this case, additive element, Ag was soluted into Fe-based matrix. With the increase in additive element, Ag, insoluble nano-crystalline Ag particles were dispersed in the Fe-based amorphous matrix. Crystallization of Fe-based amorphous phase in the matrix of $Fe_{82}Zr_7B_6Ag_5$ thin films occurred at an annealing temperature of $400^{\circ}C$. Upon annealing, the amorphous-Ag crystalline state of Fe-Zr-B-Ag films was transformed into the mixture of Ag crystalline phase + Fe-based amorphous phase + ${\alpha}$-Fe cluster followed by the crystallization process of ${\alpha}$-Fe nanocrystalline + Ag crystalline phases.

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저온균일침전법으로 제조된 루틸상 TiO2분말의 분산 안정성 (Dispersion Stability of Rutile TiO2Powder Obtained by Homogeneous Precipitation Process at Low Temperature)

  • 배현숙;박순동;김흥희;이창규;김선재
    • 한국세라믹학회지
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    • 제39권1호
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    • pp.38-44
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    • 2002
  • 여러 종류의 전해질이 존재할 때, 수계 및 비수계 분산매체에서 저온균일침전법으로 제조된 침상형태의 일차입자를 갖는 나노 크기의 루틸상 TiO$_2$분말에 대한 분산 안정성을 조사하였다. 제타전위 측정은 수계 및 비수계 분산매체에 전해질 첨가가 TiO$_2$입자 표면의 전위 역전을 유발하는 것을 보여주었다. 비수계 분산매체에 분산되어 있는 TiO$_2$입자 사이에 작용하는 정전기적 반발력은 수계 분산매체에서보다 크게 관찰되었고, 이것은 점도, 유전 상수와 같은 유기 용매의 물리적 특성과 밀접한 연관이 있음을 알 수 있었다. pH, 전해질의 농도와 이온의 원자가는 TiO$_2$입자의 표면전위를 크게 변화시켰고, TiO$_2$입자의 분산 거동을 사실상 주도하였다.

초임계 이산화탄소를 이용한 2-Hydroxypropyl-β-Cyclodextrin 미립자와 이부프로펜과의 포접복합체 제조 (Utilization of Supercritical Carbon Dioxide for the Preparation of 2-Hydroxypropyl-β-Cyclodextrin Microparticles and Their Inclusion Complexes with Ibuprofen)

  • 유종훈
    • 청정기술
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    • 제19권3호
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    • pp.212-218
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    • 2013
  • 초임계 이산화탄소를 역용매로 이용하는 aerosol solvent extraction system (ASES) 방법을 사용하여 HP-${\beta}$-CD 미립자를 제조하였으며, 공정변수가 입자의 크기와 형태에 미치는 영향을 조사하였다. 또한, 초임계 이산화탄소를 이용하여 이부프로펜과 HP-${\beta}$-CD의 포접복합체를 제조하였으며, ASES 공정에 의해 변형된 HP-${\beta}$-CD의 입자 형상이 포접효율에 미치는 영향에 대해 고찰하였다. ASES 공정으로 제조된 HP-${\beta}$-CD 미립자는 50~200 nm 크기의 나노 입자들이 응집된 입자 형상을 나타내었다. 에탄올 수용액을 HP-${\beta}$-CD의 용매로 사용한 경우 구형의 입자가 제조되었으며, 물의 양이 증가함에 따라 입자의 크기가 증가하였다. 초임계 이산화탄소를 이용해 고체상태에서 이부프로펜/HP-${\beta}$-CD 포접복합체를 제조하는 경우 초임계 ASES 방법에 의한 미세입자화 공정을 통해 포접효율을 향상시킬 수 있는 가능성을 확인하였다.

열분해와 Hot Injection법을 이용한 CoSb3 나노분말합성 (Thermal Decomposition Synthesis of CoSb3 Nanoparticle by Hot Injection Method)

  • 김민숙;안종필;김경자;박주석;김경훈;김형순
    • 한국세라믹학회지
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    • 제50권6호
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    • pp.476-479
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    • 2013
  • $CoSb_3$ with its high electrical conductivity, Seebeck coefficient and rather low thermal conductivity is quite a promising material for thermoelectric conversion applications. A potentially high figure of merit (ZT) can be achieved by a nanostructure evolution of thermoelectric materials. In this work, $CoSb_3$ nanoparticles were synthesized through a thermal decomposition method in cooperation with a hot injection technique. Nano-sized $CoSb_3$ particles were obtained through the thermal decomposition reaction between the pre-heated cobalt-oleate at $320^{\circ}C$ and the injected antimony oleate with room temperature. The results showed that the particle size was increased with increasing synthesis temperature and the crystallinity of particles was improved with temperature but the decomposition of $CoSb_3$ was observed at $320^{\circ}C$. The $CoSb_3$ particles synthesized at $300^{\circ}C$ showed a high purity and an homogeneous shape with average particle size of 26 nm.