• 한국세라믹학회지
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• 제44권12호
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• pp.740-746
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• 2007

The potential candidates for IT-SOFCs cathode materials, $Ba_{0.5}Sr_{0.5}Co_{0.8}Fe_{0.2}O_{3-{\delta}}$ (BSCF) and $La_{0.6}Ba_{0.4}Co_{0.2}Fe_{0.8}O_{3-{\delta}}$ (LBCF) powders, were synthesized by a EDTA-citrate combined method from $Sr(NO_3)_2$, $Ba(NO_3)_2$, $La(NO_3)_3{\cdot}6H_2O$, $Co(NO_3)_2{\cdot}6H_2O$, $Fe(NO_3)_3{\cdot}9H_2O$, citric acid and $EDTA-NH_3$. The cathode performance of symmetrical electrochemical cells consisting of BSCF-GDC or LBCF-GDC composite electrodes and a GDC electrolyte was investigated using by AC impedance spectroscopy at the temperature range of 500 to $700^{\circ}C$. It was found that a single phase perovskite could be successfully synthesized when the precursor is heated at $850^{\circ}C$ for 2 h. Due to thermal expansion mismatch between BSCF and GDC, the composite cathodes with lower GDC content than 45 wt% were peeled off from the GDC electrolyte and their electrode polarization resistance was estimated to be high. The thermal expansion coefficient of BSCF-GDC composites was decreased with increasing the GDC content and the electrode peeling off did not occur in BSCF-45 and 55 wt% GDC composites. BSCF-45 wt% GDC composite electrode showed the lowest area specific resistances (ASR) of 0.15 and $0.04{\Omega}{\cdot}cm^2$ at 600 and $700^{\circ}C$, respectively. On the other hand, LBCF-GDC composite cathodes showed higher ASR than the BSCF-45 and 55 wt% GDC and their cathode performance were decreased with the GDC content.

• 한국습지학회지
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• 제21권2호
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• pp.152-156
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• 2019

본 연구는 수중 암모늄 이온을 처리하기 위하여 자성 제올라이트를 합성하여 흡착 특성을 평가하였다. 표면개질된 자성 제올라이트는 수열작용으로 합성되었다. 제올라이트와 $Fe_3O_4$ 복합체는 SEM과 XRD 분석 결과 혼합비 12.6% 범위이내에서 최적인 상태로 침투 혼합된 것으로 관찰되었다. 최적의 흡착 pH는 중성부근인 약 8근처에서 나타났고, 최대 흡착량은 $Fe_3O_4$ 함량의 증가에 따라 감소하였다. 수중 암모늄 이온은 Langmuir 식에 근사하는 흡착식으로 나타났다. 개발된 합성제올라이트 흡착제는 질소농도의 관리가 필요한 습지환경 보호에도 적용 가능할 것으로 판단된다.

• 한국자기학회지
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• 제8권4호
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• pp.192-197
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• 1998

Ni1-xCdxFeAlO4계의 Mossbauer 스펙트럼은 x가 0.2이하인 경우에는 초상자성 이완 현상을, x가 0.3∼0.5인 경우는 준강자성에 의한 sextet를, x가 0.7, 0.8인 경우에는 강자성 이완 현상, x가 0.8이상인 경우에는 상자성에 dmlgksdoublet가 나타난다. x가 0.2이하인 시료에서 치환된 Cd2+이온은 주로 A-site의 Fe3+이온도 B-site로 이동하게 된다. Ni1-xCdxFeAlO4계의 초상자성 이완 현상은 A-site의 A13+이온에 의한 것으로, 강자성 이완현상은 치환된 Cd2+이온에 의한 것으로 설명할 수 있고, Yafet-Kittel 자기구조에 따라 Ni1-xCdxFeAlO4계의 자기적 성질을 해석할 수 있다.

• 한국세라믹학회지
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• 제29권7호
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• pp.511-516
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• 1992

In this study, SiC powder and Si powder were used as the raw materials. Mixture was prepared with addition of Al2O3 and Fe2O3 at 0.1~0.5wt% respectively. After this step, the mixture was pressed and nitrided for 30 hrs at 140$0^{\circ}C$ under NH3-N2 atmosphere. Mechanical properties of sintered specimens were investigated from measurement of porosity, bulk density and three point bending test. nitration reaction extent was observed at the change of mass before and after reaction, and the microstructure and the change of $\alpha$-Si3N4 and $\beta$-Si3N4 were observed by XRD and SEM. In the current work, the results are as follows 1. When Fe2O3 added, the nitridation increased with the content of Fe2O3, and the bending strength was increased from 0.1 wt% to 0.3 wt%, and decreased to 0.5 wt%. 2. When Al2O3 added, the nitridation and the bending strength increased little by little with the content of Al2O3 3. The bending strength of the specimen added with Fe2O3 were higher than that with Al2O3. Because the specimens contained Fe2O3 had much more the whisker type crystal of Si3N4 contributing to strength than contained Al2O3.

• 한국자기학회지
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• 제6권6호
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• pp.382-387
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• 1996

본 연구에서는 ${(Ni_{x}Cu_{0.2}Zn_{0.8-x}O)}_{1-w}{(Fe_{2}O_{3})}_{1+w}$의 Ni 함량(x)과 $Co_{3}O_{4}$ 첨가량에 따른 복소투자율 변화에 관하여 검토하였다. Ni 함량 x=0.6 이상에서는 매우 좁은 투자율 허수항($\mu$") 피이크가 형성됨으로서 다른 조성에 비해 손실이 적음을 알 수 있었고 공명주파수($f_{\mu"max}$)는 Ni 함량의 변화와 비례하여 현저하게 증가하였다. $Fe_{2}O_{3}$ 결핍량(w)이 많을 수록 $\mu$" 값은 낮았으나, $Fe_{2}O_{3}$ 결핍량(w)의 변화가 공명주파수에는 큰 영향을 미치지 않는 경향을 나타내었다. NiCuZn 페라이트 조성에 대하여 $Co_{3}O_{4}$를 첨가한 경우는 첨가량이 많아짐에 따라 초기투자율이 감소하여 $f_{\mu"max}$ 값은 증가하였으나, 전체적인 손실의 정도를 제어하는데에는 Ni 함량을 변화시키는 것이 더 효과적임을 알 수 있었다.

• Carbon letters
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• 제5권2호
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• pp.81-87
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• 2004

The effect of compositions of $Al_2O_3$ in the mixed $Fe/Al_2O_3$ catalysts on the synthetic behaviors of carbon nanotubes (CNTs) by catalytic chemical vapor deposition (CCVD) process was investigated in wide range of the mixture ratios of support materials. CNTs were synthesized with $Fe/Al_2O_3$ catalysis under the condition of 40 min in synthetic time, and 923 K of synthetic temperature using $C_2H_4$ and $H_2$ as synthetic and carrier gas, respectively. The carbon yield with the content of $Al_2O_3$ showed in a parabolic curve and the maximum carbon yield was 40 wt.% of $Al_2O_3$. As the mixture ratio of $Al_2O_3$ increased, decreasing tendency was observed in the diameter of CNTs. Specific surface areas of CNTs were increased with the increase of the mixture ratio of $Al_2O_3$.

• 한국자기학회지
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• 제16권1호
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• pp.18-22
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• 2006

바나듐(V)도핑이 $Fe_3O_4$의 자기적 성질에 미치는 영향을 조사하기 위하여 졸-겔 방법을 이용하여 $V_xFe_{3-x}O_4$ 박막들을 제작하고, x-ray diffraction(XRD), x-ray photoelectron spectroscopy(XPS), conversion electron Mossbauer spectroscopy(CEMS), vibrating sample magnetometry(VSM) 등을 이용하여 그 구조적, 자기적 특성들을 측정 및 분석하였다. XRD 측정 결과에 따르면 $V_xFe_{3-x}O_4$ x=1.0까지 입방(cubic)구조를 유지하며, 그 격자 상수는 거의 변화하지 않았다. 바나듐의 2p 및 철의 2p 준위들에 대한 XPS 측정 및 분석 결과, 바나듐은 화합물 내에서 주로 +3가의 상태로 존재하며, 성분비 x가 증가함에 따라 +2가 이온의 농도가 증가함이 나타났다. CEMS측정 결과 $V^{3+}$이온들은 사면체 $Fe^{3+}$자리를 주로 치환하며, $Fe^{2+}$이온들은 팔면체 $Fe^{2+}$자리를 치환하는 것으로 나타났다. 박막들에 대한 상온에서의 VSM측정 결과, 바나듐을 작은 양 도핑 할 경우(x=0.14) $V_xFe_{3-x}O_4$의 포화자화량(saturation magnetization)은 $Fe_3O_4$ 비하여 증가함이 나타났으며, 다량 도핑 할 경우$(x\geq0.5) Fe_3O_4$에 비하여 점차적으로 감소함이 나타났다. $V_xFe_{3-x}O_4$의 보자력(coercivity)은 x의 증가에 따라 증가함이 나타났는데, $V^{2+}(d^3)$ 이온의 팔면체 자리 치환에 의한 비등방성의 증가에 기인하는 것으로 해석된다.

• 한국재료학회지
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• 제23권2호
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• pp.128-134
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• 2013

A study on the corrosion behavior of Inconel alloys and Incoloy 800H in molten salt of LiCl-$Li_2O$ was investigated at $650^{\circ}C$ for 24-312 hours in an oxidation atmosphere. The order of the corrosion rate was Inconel 600 < Inconel 601 < Incoloy 800H < Inconel 690. Inconel 600 showed the best performance suggesting that the content of Fe, Cr and Ni are the important factor for corrosion resistance in hot molten salt oxidation conditions. The corrosion products of Inconel 600 and Inconel 601 were $Cr_2O_3$ and $NiFe_2O_4$, In case of Inconel 690, a single layer of $Cr_2O_3$ was formed in the early stage of corrosion and an outer layer of $NiFe_2O_4$ and inner layer of $Cr_2O_3$ were formed with an increase of corrosion time. In the case of Incoloy 800H, $Cr_2O_3$ and $FeCr_2O_4$ were observed. Most of the outer scale of the alloys was observed to be spalled from the results of the SEM analysis and the unspalled scale which adhered to the substrate was composed of three layers. The outer layer, the middle one, and the inner one were Fe, Cr, and Ni-rich, respectively. Inconel 600 showed localized corrosion behavior and Inconel 601, 690 and Incoloy 800H showed uniform corrosion behavior. Ni improves the corrosion resistance and too much Cr and/or Fe content deteriorates the corrosion resistance.

• 대한금속재료학회지
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• 제49권2호
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• pp.153-160
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• 2011

The AISI 216L stainless steel with a composition of Fe-16Cr-6Ni-6Mn-1.7Mo (wt.%) was oxidized at $700{\sim}900^{\circ}C$ in air for 100 h. At $700^{\circ}C$, a thin $Mn_{1.5}Cr_{1.5}O_4$ oxide layer with a thickness of $0.4{\mu}m$ formed. At $800^{\circ}C$, an outer thin $Fe_2O_3$ oxide layer and a thick inner $FeCr_2O_4$ oxide layer with a total thickness of $30{\mu}m$ formed. The non-adherent scale formed at $800^{\circ}C$ was susceptible to cracking. At $900^{\circ}C$, an outer thin $Fe_2O_3$ oxide layer and a thick inner $Mn_{1.5}Cr_{1.5}O_4$ oxide layer formed, whose total thickness was $10{\sim}15{\mu}m$. The scales formed at $900^{\circ}C$ were non-adherent and susceptible to cracking. 216 L stainless steel oxidized faster than 316 L stainless steel, owing to the increment of the Mn content and the decrement of Ni content.

• 한국세라믹학회지
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• 제36권4호
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• pp.410-416
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• 1999

The reactivity of three kinds of spinels which CaO-Al2O3-SiO2 slag was investigated in terms of mineral phases and microstructures. New crystal products were not formed by reaction of 12CaO.7Al2O3 in the slag with spinels and free MgO components was preferenctially dissolved into slag for MgO-rich spinel and stoichiometric spinel. Meanwhile mineral phase was changed from 12CaO.7Al2O3 to CaO.Al2O3 to CaO.2Al2O3 finally to CaO.6Al2O3 having high melting point for Al2O3 -rich spinel. The Fe-oxide component of the slag was taken up by only stoichiometric spinel grains within the spinel clinker and the trapped amount of Fe-oxide was independent of MgO content of MgO in spinel clinker the more th resistance to slag corrosion but the less resistance to slag penetration.