• 천문학회지
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• 제29권2호
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• pp.207-215
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• 1996

To derive coronal temperature, electron density and nonthermal velocity, we have analyzed high resolution spectra (e.g., Fe XII 338.3, Fe XII 352.1, Fe XIV 334.2, Fe XIV 353.8, Fe XV 284.2, Fe XV 321.8, Fe XV 327.0, Fe XVI 335.4, and Fe XVI 360.8) taken from AR 6615 by SERTS (Solar Extreme Ultraviolet Rocket Telescope and Spectrograph). Important findings emerging from the present study are as follows: (1) Temperature estimated from Fe XVI 335.4 and Fe XIV, 334.2 is $\~2.4\times10^6 K$ and no systematic difference in temperature is found between the active region and its adjacent quiet region; (2) Mean electron density estimated from Fe XV is $\~3\times10^9 cm^{-3}\;and\;\~10^{10} cm^{-3}$ from Fe XII and Fe XIV; (3) Mean density of the active region is found to be higher than that of the quiet region by a factor of 2; (4) Nonthermal velocity estimated from Fe XV and Fe XVI is $20\times25 km\;s^{-l}$ which decreases with increasing ionization temperatures. This supports the notion that the nonthermal velocity declines outwards above the transition region.

• 청정기술
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• 제18권1호
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• pp.89-94
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• 2012

본 연구에서는 산성을 갖는 Fe-ZSM5를 담체로 활용하여 Pd, Pt 등 귀금속을 담지한 후, 제조 촉매의 암모니아의 선택적 산화반응 활성을 평가하였다. 이들 중 Pt/Fe-ZSM5가 Pd/Fe-ZSM5 보다 높은 활성을 나타냈다. 또한 Pt/Fe-ZSM5 촉매에서 ZSM5 구조체 내 Fe의 이온교환량을 달리한 촉매의 실험을 수행하여, 암모니아의 선택적 산화반응에 가장 우수한 활성을 보이는 최적 조성비를 탐색하였다. 그 결과, Fe의 이온교환량이 적을수록 반응 활성이 증가하는 경향을 보였고, 저온 영역인 $250^{\circ}C$에서 100%의 암모니아 전환율을 나타냈다. 이와 같이 암모니아의 선택적 산화반응에 효과적인 Fe-ZSM5 담체에 대하여, ICP-AES, BET, XRD, $NH_3$-TPD 등과 같은 특성 분석을 수행하여 제조 촉매의 구조와 물성이 반응활성에 미치는 영향을 검토해보았다.

• Journal of Magnetics
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• 제16권3호
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• pp.229-233
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• 2011

Phase evolution during the hydrogen-assisted disproportionation of $Nd_{12.5}Fe_{80.6}B_{6.4}Ga_{0.3}Nb_{0.2}$ alloy was investigated mainly by using a magnetic balance-type thermomagnetic analyser (TMA). In order to avoid any undesirable phase change in the course of heating for TMA, a swift TMA technique with very high heating rate (around 2 min to reach $800^{\circ}C$ from room temperature) was adopted. The hydrided $Nd_{12.5}Fe_{80.6}B_{6.4}Ga_{0.3}Nb_{0.2}$ alloy started to be disproportionated in hydrogen from around $600^{\circ}C$, and the alloy after the early disproportionation (from 600 to $660^{\circ}C$) has been partially disproportionated. The partially disproportionated alloy consisted of a mixture of $NdH_x$, $Fe_3B$, ${\alpha}$-Fe, and the remaining undisproportionated $Nd_2Fe_{14}BH_x$-phase. During the subsequent heating to $800^{\circ}C$ in hydrogen, two additional phases of $Fe_{23}B_6$ and $Fe_2B$ were formed, and the material consisted of a mixture of $NdH_x$, $Fe_{23}B_6$, $Fe_3B$, $Fe_2B$, and ${\alpha}$-Fe phases. During the subsequent isothermal holding at $800^{\circ}C$ for 1 hour, the phase constitution was further changed, and one additional unknown magnetic phase was formed. Eventually, the fully disproportionated $Nd_{12.5}Fe_{80.6}B_{6.4}Ga_{0.3}Nb_{0.2}$ alloy consisted of $NdH_x$, $Fe_{23}B_6$, $Fe_3B$, $Fe_2B$, ${\alpha}$-Fe, and one additional unknown magnetic phase.

• 한국주조공학회지
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• 제23권2호
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• pp.77-85
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• 2003

Some alloying elements such as Cr, B, Ti and Si were added individually or as a mixture to Fe-30 at.%Al alloys. The alloys were melted using an arc furnace and then heat-treated for homogenization at 1000$^{\circ}C$ for 7 days and followed by rolling at 1000$^{\circ}C$. The alloying elements on rolling characteristics were investigated by the microstructures and fracture mode before and after rolling. The microstructures before rolling showed that all of the alloys had equiaxed grains. On the other hand, the microstructures of rolling plane as well as its perpendicular plane became elongated after rolling. The alloys such as Fe-30Al, Fe-30Al-3Ti, Fe-30Al-0.5B, Fe-30Al-5Cr and Fe-30Al-3Ti-0.5B revealed better rolling behaviour from the point that intergranular and cleavage fractures were not fundamentally occurred. But the addition of 5Ti or 3Si to Fe-Al alloys had detrimental effects. The Ti-added alloy system such as Fe-30Al-5Ti, Fe-30Al-5Ti-5Cr, Fe-30Al-3Ti-5Cr and Fe-30Al-5Ti-0.5B were cracked through grain and showed cleavage fracture. The Si-added alloy system such as Fe-30Al-5Si, Fe-27Al-3Si and Fe-27Al-5Cr-3Si were cracked along the grain boundary and showed intergranular fracture. $DO_3{\leftrightarrow}B_2$ transition temperature of Fe-30at.%Al alloy was 520$^{\circ}C$, whereas the addition of 3Ti and 3Ti+0.5B comparably increased the temperature to 797 and 773$^{\circ}C$, respectively.

• Journal of Photoscience
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• 제1권2호
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• pp.83-88
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• 1994

The synergic effect of iron plus blue light on the peroxidation of membrane lipid was investigated, using liposomes made of phospholipid. While strong irradiation did not affect Fe$^{+2}$-promoted lipid peroxidation that turned out to be O$_2$-dependent, ferric iron in bright light exerted a pronounced effect on the initiation of lipid peroxidation: this combined action of light and Fe$^{+3}$ on liposomal membranes was apparently independent of O$_2$. When liposomal samples containing Fe$^{+3}$ were subjected to irradiation, some portions of Fe$^{+3}$ were converted into Fe$^{+2}$. The extent of the Fe$^{+3}$-Fe$^{+2}$ conversion increased with increasing time of irradiation, which resembled the dependence of Fe$^{+3}$-promoted lipid peroxidation on irradiation. Further, it was observed that the effect of irradiation in liposomal samples containing Fe$^{+2}$ was strikingly mimicked by that of Fe$^{+2}$ addition to the same samples. The obligatory requirement of a suitable Fe$^{+3}$/Fe$^{+2}$ ratio for the genesis of iron-dependent lipid peroxidation, a controversial proposition, was also confirmed by the observation that lipid peroxidation was substantially enhanced by the addition of a mixture of Fe$^{+3}$ and Fe$^{+2}$, as compared to the addition of Fe$^{+3}$ or Fe$^{+2}$ alone. The results obtained in this study not only suggest that light acts as an effector for initiating lipid peroxidation, when Fe$^{+3}$ is present in membrane systems, but also imply that any chemical or physical factor that influences the redox states of iron in membranes can play a role in lipid peroxidation reactions.

• 센서학회지
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• 제30권4호
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• pp.191-195
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• 2021

Pure ZnFe₂O₄ and Fe₂O₃-ZnFe₂O₄ hetero-composite spheres were prepared by ultrasonic spray pyrolysis of a solution containing Zn- and Fe-nitrates. Additionally, the sensing characteristics of these spheres in the presence of 5 ppm ethanol, benzene, p-xylene, toluene, and CO (within the temperature range of 275-350 ℃) were investigated. The Fe₂O₃-ZnFe₂O₄ hetero-composite sensor with a cation ratio of [Zn]:[Fe]=1:3 exhibited a high response (resistance ratio = 140.2) and selectivity (response to p-xylene/response to ethanol = 3.4) to 5 ppm p-xylene at 300 ℃, whereas the pure ZnFe₂O₄ sensor showed a comparatively lower gas response and selectivity. The reasons for the superior response and selectivity to p-xylene in Fe₂O₃-ZnFe₂O₄ hetero-composite sensor were discussed in relation to the electronic sensitization due to charge transfer at Fe₂O₃-ZnFe₂O₄ interface and Fe₂O₃-induced catalytic promotion of gas sensing reaction. The sensor can be used to monitor harmful volatile organic compounds and indoor air pollutants.

• 한국재료학회지
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• 제34권6호
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• pp.309-314
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• 2024

The structure and magnetic properties of composite powders prepared by ball milling a mixture of Fe₂O₃·(0.4-1.0)Fe were investigated. Hysteresis loops and differential scanning calorimetry (DSC) curves are used to characterize the materials and to examine the effect of the solid state reaction induced by ball milling. The results showed that a solid state reaction in Fe₂O₃·(0.4-1.0)Fe clearly proceeds after only 1 h of ball milling. The system is characterized by a positive reaction heat of +2.23 kcal/mole. The diffraction lines related to Fe₂O₃ and Fe disappeared after 1 h of ball milling and, instead, diffraction lines of the intermediate phase of Fe₃O₄ plus FeO formed. The magnetization and coercivity of the Fe₂O₃·0.8Fe powders were changed by the solid state reaction process of Fe₂O₃ by Fe during ball milling. The coercivity of the Fe₂O₃·0.8Fe powders increased with increasing milling time and reached a maximum value of 340 Oe after 5 h of ball milling. This indicates the grain size of Fe₃O₄ was clearly reduced during ball milling. The magnetic properties of the annealed powders depend on the amount of magnetic Fe and Fe₃O₄ phases.

• 한국자기학회지
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• 제8권4호
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• pp.198-202
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• 1998

AlxFe3-xO4를 직접합성법으로 제조하여 x-선 회절법과 Mossbauerqnsrhkd법으로 연구하였다. Mossbauer spectrum에서 subspectrum 흡수면적비에 의하여 이온분포를 졀정하였다. 팔면체자리(B-site)에 들어 있는 Fednjs자는 Aldnjs자의 첨가량과 관계없이 hopping Fe2+ (Fe3+,Al3+)에 의한 Fe2.5+의 전하상태에 있다.

• 한국균학회지
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• 제21권3호
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• pp.165-171
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• 1993

표고버섯 중의 광감응성 mitochondrial ATP synthase는 0.1 mM $Fe^{2+}$ 단독 이온에 의하여 그 활성이 대조구에 비해 102%, 증가되었으며, 반면 $Fe^{3+}$ 및 $Mg^{2+}$ 이온은 효소의 활성을 억제시켰다. 0.5 mM $Mg^{2+}$ 존재하에서 0.1 mM $Fe^{2+}$ 이온에 의한 이 효소의 활성은 32% 증가되었으며 0.5 mM $Mg^{2+}$ 존재하에서 $Fe^{3+}$ 이온효과는 단독 $Fe^{3+}$ 이온의 효과와 유사한 경향으로 효소의 활성을 저해하였다. 0.5 mM $Mg^{2+}$과 0.1 mM, 0.5 mM 및 1.0 mM $Fe^{3+}$ 이온의 공존하에서$Fe^{2+}$ 이온에 의한 효소의 활성은 모두 억제되었으며, 특히 0.5 mM $Mg^{2+}$과 0.1 mM $Fe^{3+}$ 이온의 공존하에서 5.0 mM $Fe^{2+}$ 이온에 의하여 53%의 억제현상을 나타내었다. 따라서 표고버섯 중의 광감응성 mitochondrial ATP synthase의 활성은 $Fe^{2+}$ 이온에 의하여 특이적으로 크게 증가되며, 이 효소에 대한 $Fe^{2+}$ 이온의 활성화 효과가 $Mg^{2+}$ 이온에 의하여 크게 영항을 받지 않으나, $Fe^{3+}$ 이온의 공존하에서는 억제됨을 알았다. 활성화 금속이온인 $Fe^{2+}$ 존재하에서 이 효소의 최적 pH는 7.6이며, 최적 온도는 $63^{\circ}C$이었다. 또한 이 효소는 금속 chelating agent인 EDTA에 의하여 효소의 활성이 상실됨으로써 metalloenzyme의 가능성을 제시하였다.

• 자원리싸이클링
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• 제26권4호
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• pp.95-100
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• 2017

본 연구에서는 폐 PCB(printed circuit board) 표면을 긁어내어 회수한 구리분말을 용융하는 과정에서 용융온도 저감과 정제를 위하여 플럭스로 $Fe_2O_3$를 첨가하였으며, $Fe_2O_3$ 첨가량 및 온도에 따른 구리의 회수율과 불순물 농도에 미치는 영향을 조사하였다. 구리 회수율은 반응온도와 $Fe_2O_3$의 첨가비율이 증가할 수 록 증가하였다. 그리고 구리 중 산소, 실리콘, 철의 농도는 $Fe_2O_3$ 첨가량이 증가할수록 감소하였다. $Fe_2O_3$를 첨가하여 반응시킨 후의 슬래그를 XRD로 분석하여 fayalite($2FeO{\cdot}SiO_2$)와 철산화물을 확인하였다. 따라서 fayalite 슬래그의 생성에 의한 슬래그의 융점과 점도 감소가 구리 회수율의 증가에 크게 기여한 것으로 생각된다.