• 대한화학회지
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• 제25권5호
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• pp.318-324
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• 1981

일차입자의 크기와 응집상태가 다른 두 종류의 $Fe_2O_3$를 부분침전법과 ball-mill 혼합법으로 BaCO$_3$와 혼합한 $BaCO_3-Fe_2O_3$계의 고체반응에 있어 $Fe_2O_3$분체의 영향을 조사하였다. TG, XRD, SEM 등을 측정에 사용하였으며, X-선 회절분석결과 Ba-ferrite의 생성과정은 다음과 같은 연속적인 2단계로 이루어진다는 것을 알았다. $BaCO_3 + 6Fe_2O_3\;{\longrightarrow}\;BaFe_2O_3 + 5Fe_2O_3 + CO_2{\uparrow}\;BaFe_2O_4 + 5Fe_2O_3 \;{\longrightarrow}\;BaFe_{12}O_{19}$ 또 $Fe_2O_3$원료분체의 응집상태와 혼합방법은 고체반응에 현저한 영향을 미친다는 것을 확인했다.

• 한국세라믹학회지
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• 제34권7호
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• pp.738-746
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• 1997

MgO clinker and two kinds of dolomite clinkers with different microstructures and CaO contents were used as starting materials, and the effects of Fe2O3 addition on the properties of MgO and dolomite were investigated in the range of 2 to 8 wt% of Fe2O3 content. Secondary phases contributed to densification of MgO-Fe2O3 and dolomite-Fe2O3 were magnesioferrite and dicalciumferrite, respectively. Sinterabilities of MgO-Fe2O3 and dolomite-Fe2O3 were directly proportional to the amount of secondary phases. Also, sinterability of dolomite itself was dependent on the microstructure of starting material including distribution of CaO and MgO as well as the addition amount of Fe2O3. The flexural strength of MgO-Fe2O3 content was almost constant. The hydration resistance of dolomite with large size of MgO and discontinuous distribution of CaO was higher than that of dolomite with small size of MgO and continuous distribution of CaO. Also, the minimum content of Fe2O3 to prevent they hydration of dolomite was about 4wt%. As increasing Fe2O3 content, the penetration resistance of MgO-Fe2O3 was improved by the increment of magnesioferrite. On the other hand, the penetration resistance of dolomite-Fe2O3 was decreased because of the increment of dicalciumferrite having low melting point.

• 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.

• 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.

• 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 $O_2$.

• 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.

• 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.

• 대한화학회지
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• 제27권3호
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• pp.194-200
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• 1983

${\alpha}-Fe_2O_3$의 HCl 또는 $H_2SO_4$에 의한 용해반응에 있어서 금속염의 첨가효과를 분광광도법과 중량법으로 검토하였다. 환원성 금속염은 현저한 반응촉진 효과를 보이나 비환원성 금속염은 부의 효과를 나타내었다. $FeCl_2$와 같은 환원성 금속염을 첨가한 경우에 ${\alpha}-Fe_2O_3$의 용해속도가 크게 촉진되는 것은 $Fe^{3+}$ 와 $Fe^{2+}$ 사이에 chloro-brige가 형성되어 전하이동이 일어나면서 ${\alpha}-Fe_2O_3$ 표면의 격자에너지를 감소시키기 때문인 것으로 추측된다. 이 전하이동으로 인한 ${\alpha}-Fe_2O_3$ 표면의 격자 에너지 변화가 반응의 활성화에너지 변화와 대응된다고 보면 약 0.36e의 부분전하가 $Fe^{3+}$ 쪽으로 옮겨간 것으로 계산되었다.

• 한국결정성장학회지
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• 제9권2호
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• pp.185-190
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• 1999

$Al_2O_3/Fe$ 복합재료 제조는 반응소결법에 의한 2단계 공정을 통해서 제조되었으며 이 공정은 장비가 간단하고 near-net-shape이 가능한 장점이 있다.$Al_2O_3/Fe$ 복합재료를 제조하기 위해서 1차로 $650^{\circ}C$에서 5시간동안 산화/환원 처리를 행하고 $1200^{\circ}C$에서 2차로 소결처리를 행하였다. 제조된 복합재료의 상분석결과 $\alpha$-Fe 와 $\alpha$-$Al_2O_3/Fe$가 주된 상이었고 소량의 $FeAl_2O_4$가 검출되었다. 이 소량의 $FeAl_2O_4$상은 Fe가 $Al_2O_4$기공을 채우는 것을 방해함으로써 소결동안 미세구조 내에 약간의 기공을 발생시킨다.