• 산업기술연구
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• 제36권
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• pp.77-81
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• 2016

Superparamagnetic $Fe_3O_4$ nanoparticles with particle size from 10 to 20 nm were synthesized by coprecipitation method. Subsequently, the $Fe_3O_4$ nanoparticles were used to fabricate $Fe_3O_4/SiO_2$ core-shell nanoparticles by sol-gel method. The $Fe_3O_4/SiO_2$ nanoparticles synthesized by sol-gel method exhibit the high uniformities of particle size and shape. We also investigated the heating characteristics of $Fe_3O_4$ and $Fe_3O_4/SiO_2$ nanoparticles for biomedical applications. The $Fe_3O_4$ nanoparticles show the faster temperature increase and the higher specific loss power(SLP) value than the $Fe_3O_4/SiO_2$ nanoparticles.

• 한국재료학회지
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• 제22권11호
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• pp.620-625
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• 2012

A general synthetic method to make $Fe_3O_{4-{\delta}}$ (activated magnetite) is the reduction of $Fe_3O_4$ by $H_2$ atmosphere. However, this process has an explosion risk. Therefore, we studied the process of synthesis of $Fe_3O_{4-{\delta}}$ depending on heat-treatment conditions using $FeC_2O_4{\cdot}2H_2O$ in Ar atmosphere. The thermal decomposition characteristics of $FeC_2O_4{\cdot}2H_2O$ and the ${\delta}$-value of $Fe_3O_{4-{\delta}}$ were analyzed with TG/DTA in Ar atmosphere. ${\beta}-FeC_2O_4{\cdot}2H_2O$ was synthesized by precipitation method using $FeSO_4{\cdot}7H_2O$ and $(NH_4)_2C_2O_4{\cdot}H_2O$. The concentration of the solution was 0.1 M and the equivalent ratio was 1.0. ${\beta}-FeC_2O_4{\cdot}2H_2O$ was decomposed to $H_2O$ and $FeC_2O$4 from $150^{\circ}C$ to $200^{\circ}C$. $FeC_2O4$ was decomposed to CO, $CO_2$, and $Fe_3O_4$ from $200^{\circ}C$ to $250^{\circ}C$. Single phase $Fe_3O_4$ was formed by the decomposition of ${\beta}-FeC_2O_4{\cdot}2H_2O$ in Ar atmosphere. However, $Fe_3C$, Fe and $Fe_4N$ were formed as minor phases when ${\beta}-FeC_2O_4{\cdot}2H_2O$ was decomposed in $N_2$ atmosphere. Then, $Fe_3O_4$ was reduced to $Fe_3O_{4-{\delta}}$ by decomposion of CO. The reduction of $Fe_3O_4$ to $Fe_3O_{4-{\delta}}$ progressed from $320^{\circ}C$ to $400^{\circ}C$; the reaction was exothermic. The degree of exothermal reaction was varied with heat treatment temperature, heating rate, Ar flow rate, and holding time. The ${\delta}$-value of $Fe_3O_{4-{\delta}}$ was greatly influenced by the heat treatment temperature and the heating rate. However, Ar flow rate and holding time had a minor effect on ${\delta}$-value.

• 한국재료학회지
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• 제22권5호
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• pp.253-258
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• 2012

Activated magnetite ($Fe_3O_{4-{\delta}}$) was applied to reducing $CO_2$ gas emissions to avoid greenhouse effects. Wet and dry methods were developed as a $CO_2$ removal process. One of the typical dry methods is $CO_2$ decomposition using activated magnetite ($Fe_3O_{4-{\delta}}$). Generally, $Fe_3O_{4-{\delta}}$ is manufactured by reduction of $Fe_3O_4$ by $H_2$ gas. This process has an explosion risk. Therefore, a non-explosive process to make $Fe_3O_{4-{\delta}}$ was studied using $FeC_2O_4{\cdot}2H_2O$ and $N_2$. $FeSO_4{\cdot}7H_2O$ and $(NH_4)_2C_2O_4{\cdot}H_2O$ were used as starting materials. So, ${\alpha}-FeC_2O_4{\cdot}2H_2O$ was synthesized by precipitation method. During the calcination process, $FeC_2O_4{\cdot}2H_2O$ was decomposed to $Fe_3O_4$, CO, and $CO_2$. The specific surface area of the activated magnetite varied with the calcination temperature from 15.43 $m^2/g$ to 9.32 $m^2/g$. The densities of $FeC_2O_4{\cdot}2H_2O$ and $Fe_3O_4$ were 2.28 g/$cm^3$ and 5.2 g/$cm^3$, respectively. Also, the $Fe_3O_4$ was reduced to $Fe_3O_{4-{\delta}}$ by CO. From the TGA results in air of the specimen that was calcined at $450^{\circ}C$ for three hours in $N_2$ atmosphere, the ${\delta}$-value of $Fe_3O_{4-{\delta}}$ was estimated. The ${\delta}$-value of $Fe_3O_{4-{\delta}}$ was 0.3170 when the sample was heat treated at $400^{\circ}C$ for 3 hours and 0.6583 when the sample was heat treated at $450^{\circ}C$ for 3 hours. $Fe_3O_{4-{\delta}}$ was oxidized to $Fe_3O_4$ when $Fe_3O_{4-{\delta}}$ was reacted with $CO_2$ because $CO_2$ is decomposed to C and $O_2$.

• 한국세라믹학회지
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• 제32권2호
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• pp.234-238
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• 1995

MgFe2O4 formation, grain growth in Fe2O3, Fe solid-solution limit in MgO for MgO-Fe2O3 mixture were studied by means of investigating the distribution of phases and compositions in reaction area between MgO and Fe2O3. The reaction area at equlibrium was composed with MgO-FexO matrix and MgFe2O4 precipitation, MgFe2O4 was formed by precipitating from MgO-FexO matrix dependent on oxygen partial pressure. Fe contents was exponentially decreased with diffusion distance in MgO single crystal, and thus Fe solid-solution limitation in MgO was about 4mol%. The grain growth rate in Fe2O3 base was increased with Mg contents diffused from MgO single crystal.

• 센서학회지
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• 제8권2호
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• pp.171-176
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• 1999

PECVD법을 이용하여 $Al_2O_3$ 기판위에 증착된 $Fe_3O_4$박막의 상전이를 통하여 ${\gamma}-Fe_2O_3$ 박막을 제조하였다. ${\gamma}-Fe_2O_3$ 박막의 상전이는 주로 증착온도와 $Fe_3O_4$의 산화과정에 의해 유도되었다. $Fe_3O_4$ 상은 $200{\sim}300^{\circ}C$의 증착온도에서 in-situ로 얻을 수 있었다. 증착온도에 따른 상변화는 없었으며 $250^{\circ}C$에서 증착된 $Fe_3O_4$상이 가장 안정된 상을 나타내었다. ${\gamma}-Fe_3O_3$ 상은 $280{\sim}300^{\circ}C$의 온도범위에서 $Fe_3O_3$ 상을 산화시켜 유도하였다. $Fe_3O_4$ 상과 ${\gamma}-Fe_2O_3$ 상은 같은 spinel구조를 가지고 있으며 공존상으로서 존재함을 알 수 있었다. 또한, $Al_2O_3$에 산화된 ${\gamma}-Fe_2O_3$ 박막은 다공성의 미세구조를 나타내었다.

• 한국세라믹학회지
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• 제31권2호
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• pp.213-219
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• 1994

The formations of spinel and colors of ZnO-Fe2O3-TiO2-SnO2 system have been researched on the basis of ZnO-Fe2O3 system. Specimens were prepared by substituting Fe3+, with Ti4+ or Sn4+ when mole ratios between Fe3+ and Ti4+ or between Fe3+ and Sn4+ were 0.2 mole. The reflectance measurement and X-ray diffraction analysis of the formation of spinel and the colors of there specimens were carried out. ZnO-Fe2O3 system in which Fe2O3 was substituted with SnO2 and TiO2 was formed the spinel structure of 2ZnO.TiO2, 2ZnO.SnO2, ZnO.Fe2O3. The stable stains which were colored with yellow and brown could be manufactured.

• Korean Chemical Engineering Research
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• 제46권6호
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• pp.1113-1118
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• 2008

$CuFe_2O_4$와 $Fe_3O_4$의 탄소 침적 및 환원 특성을 $900^{\circ}C$에서 TGA, XRD, SEM, TEM 등의 분석 및 반응 후 가스조성분석을 통하여 연구하였다. XRD 분석결과 환원된 $Fe_3O_4$는 Fe(iron)와 graphite(C) 그리고 $Fe_3C$으로 구성되어 있는 것으로 나타났다. 반면에, 환원된 $CuFe_2O_4$에서는 graphite나 $Fe_3C$가 나타나지 않았다. SEM을 이용하여 표면 구조를 관찰한 결과 환원된 $Fe_3O_4$의 표면이 탄소로 뒤덮여 있는 것을 확인할 수 있었다. 이와 달리 $CuFe_2O_4$에서는 $CH_4$ 전환율 및 환원속도가 높았고, 환원반응 후 탄소량 추정결과 $Fe_3O_4$에서보다 훨씬 낮게 나타났다. TEM 분석결과 $Fe_3O_4$ 입자로부터 탄소가 판상구조의 형태로 성장한 것을 확인할 수 있었다.

• Transactions on Electrical and Electronic Materials
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• 제15권6호
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• pp.338-343
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• 2014

A $Fe_3O_4$-graphite nanofiber composite for use as an anode material was successfully synthesized by calcining $Fe_3O_4$ and graphite nanofiber (GNF) together in a $N_2$ atmosphere. Using this $Fe_3O_4$-GNF composite in a lithium ion battery resulted in a higher lithium storage capacity than that obtained using $Fe_3O_4$-graphite ($Fe_3O_4$-G). The $Fe_3O_4$-GNF (10 wt%) electrode exhibited a higher lithium ion diffusion coefficient ($2.29{\times}10^{-9}cm^2s^{-1}$) than did the $Fe_3O_4$-G (10%) ($3.17{\times}10^{-10}cm^2s^{-1}$). At a current density of $100mA\;g^{-1}$, the $Fe_3O_4$-GNF (10 wt%) anode showed a higher reversible capacity ($1,031mAh\;g^{-1}$) than did the $Fe_3O_4$-G (10%) anode ($799mAh\;g^{-1}$). Moreover, the $Fe_3O_4GNF$ electrodes showed good cycling performance without the addition of a conductive material.

• 한국결정성장학회지
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• 제19권4호
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• pp.202-207
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• 2009

본 연구에서는 $Fe/Al_2O_3$ 및 $Fe/TiO_2$계 나노복합분말을 제조하기 위하여 실온 기계적 합금화법(MA)을 적용하였다. $Fe_3O_4-M$(M= AI, Ti)이고 여기서 순금속 Al 및 Ti은 고상반응 시 환원제로서 선택하였다. $Fe_3O_4$-순금속의 각각 25시간 및 75시간 MA 처리한 결과 $Fe/Al_2O_3$ 및 $Fe/TiO_2$ 나노복합분발이 얻어졌으며, 이것은 나노결정립의 ${\alpha}$-Fe 기지에 $Al_2O_3$ 및 $TiO_2$가 각각 미세하게 분산된 나노복합분말임을 알 수 있었다. 또한 Fe$_3$O$_4$-AI계에서 보다 짧은 반응 시간에 복합분말이 생성되는 것은 $Fe_3O_4$의 Al에 의한 환원반응 시 큰 반응열에 기인하는 것으로 사료된다. MA법으로 제조된 $Fe/TiO_2$ 복합분말의 X선 회절분석으로부터 ${\alpha}$-Fe 결정립 크기는 30 nm 임을 알 수 있었다. 또한 MA 과정 중 시료의 자기 측정으로부터 $Fe_3O_4$의 순금속 Al 및 Ti 에 의한 고상환원반응 과정을 자세히 관찰할 수 있었다.

• 대한화학회지
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• 제24권2호
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• pp.139-145
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• 1980

마크로사이클리간드인 1,4,8,11-테트라아자사이클로테트라데칸 (cyclam)과 비환형 리간드인 1,5,8,12-테트라아자도데칸 (3,2,3-tet)의 높은 스핀철(Ⅱ) 착화합물이 합성되었다. 낮은 스핀인 $[Fe(cyclam)(CH_3CN)_2](ClO_4)_2$는 메탄올속에서 염소이온과 반응하여 높은 스핀인 $[Fe(cyclam)Cl]ClO_4$를 생성한다. $[Fe(cyclam)(CH_3CN)_2](ClO_4)_2$는 낮은 스핀이지만 $[Fe(3,2,3-tet)(CH_3CN)_2](ClO_4)_2$는 높은 스핀을 가지며 이 차이는 비환형 리간드가 환형 리간드보다 압축효과가 작은 것으로 설명된다. $[Fe(cyclam)Cl]ClO_4$의 합성은 마크로사이클리간드가 불포화되어 있거나 치환체가 있어야 높은 스핀 다섯배위철(II) 착화합물의 합성이 가능하다는 지금까지의 전해에 반대되는 증거가 된다. $[Fe(cyclam)Cl]ClO_4$와 $[Fe(3,2,3-tet)(CH_3CN)_2](ClO_4)_2$는 일산화탄소와 반응해서 각기 낮은 스핀 여섯배위인 $[Fe(cyclam)Cl(CO)]ClO_4$ 와 $[Fe(3.2,3-tet)(CH_3CN)(CO)](ClO_4)_2$를 만든다.