• 한국세라믹학회지
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• 제31권12호
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• pp.1501-1506
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• 1994

The precipitate of FeCl2.4H2O and NaOH, Fe(OH)2 was rapidly made to oxidize by H2O2 to prepare $\delta$-FeOOH. The particle size, surface and morphology of $\delta$-FeOOH, and the shape and structure of thermally decomposed $\delta$-FeOOH were investigated by the use of high resolution STEM. $\delta$-FeOOH prepared under the condition of reaction temperature of Fe(OH)2 at 4$0^{\circ}C$, [OH-][Fe2+]=5 and aging time of 2 hr Fe(OH)2, had 630$\AA$ mean particle size, 4~5 aspect ratio, 20.8 emu/g saturation magnetization and 210 Oe coercivity. The edges of $\delta$-FeOOH were inclined to (001) about 41$^{\circ}$, 60$^{\circ}$ and coincident with (102), (101) respectively. When $\delta$-FeOOH was thermally decomposed at 25$0^{\circ}C$ for 2 hr in vacuo, which had micropores of 0.9 nm thickness and crystallites of 2.4 nm thickness. (001)hex, [10]hex. of $\delta$-FeOOH parallel with (001)hex, [100]hex. of $\alpha$-Fe2O3 respectively. This showed three dimensional topotaxial structure transition, which was investigated by SADP (Selected Area Diffraction Pattern) of STEM.

• 한국세라믹학회지
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• 제33권3호
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• pp.327-331
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• 1996

$\delta$-FeOOH was prepared by rapid oxidation method of Fe(OH)2 using H2O2. The effects of reaction temperature and mole ratio ([OH-]/[Fe2+])의 몰비를 제조 변수로 하여 최종 생성된 $\delta$-FeOOH의 입자크기 입자형태, 자기특성을 조사하였다. Fe(OH)2 의 반응온도 및 [OH-]/[Fe2+] 비가 $\delta$-FeOOH의 입자크기 및 형상에 많은 영향을 미침을 알수 있었으며 입자 크기는 이 두인자에 비례하여 증가하였다 Fe(OH)2 의 반응온도가 4$0^{\circ}C$ [OH-]/[Fe2+]=5 Fe(OH)2 숙성 시간 2시간에서 제조된 $\delta$-FeOOH를 TEM, VSM으로 입자의 크기 및 자기특성을 조사한결과 평균 입경이 630$\AA$ 정도이고 입도 분포가 양호하였으며 포화자화 및 보자력은 각각 20.8emu/g 210 Oe였다.

• 한국세라믹학회지
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• 제32권12호
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• pp.1383-1391
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• 1995

Hexagonal $\delta$-FeOOH was coated with Ba-Sol, which was produced by hydrolizing Ba(OC2H5)2, Ba-Sol coated $\delta$-FeOOH spread on a stainless plate, dried at 8$0^{\circ}C$ and then heat-treated. In this way, Ba-ferrite fine particles were produced. although there was a difference in a degree of hydrolysis of Ba(OC2H5)2, crystalline phase of Ba-ferrite appeared around 617$^{\circ}C$, and Ba-ferrite single phase was obtained after heat treatment at 80$0^{\circ}C$ for 2 hr. When Ba-ferrite was made from Ba-Sol coated $\delta$-FeOOH, $\delta$-FeOOH was thermally decomposed to $\alpha$-Fe2O3 at $700^{\circ}C$, producing a porous structure which was observed by TEM photographs. But the porous structure was not observed at 80$0^{\circ}C$. Ba-ferrite, heat-treated at 80$0^{\circ}C$ for 2 hr, had mean particle size of 1000$\AA$, lattice parameter of a0=5.889243 $\AA$ and c0=23.214502 $\AA$, a saturation magnetization ($\sigma$8) of 45.3 emu/g and a coercive force (Hc) of 5200Oe.

• 한국세라믹학회지
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• 제38권11호
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• pp.1015-1022
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• 2001

본 연구에서는 용융염법에 의한 Ba-ferrite의 생성기구와 그 자기적특성에 대해 조사하였다. 출발원료 중 BaC $O_3$만이 용융염내에서 용해도를 가졌으며, 이는 용융염내에서는 Ba-ferrite의 생성이 용해된 $Ba^{2+}$가 F $e_2$ $O_3$나 $\delta$-FeOOH의 표면으로 확산하여 표면반응을 통해 일어나는 것으로 보인다. 한편, 출발물질($\delta$-FeOOH와 F $e_2$ $O_3$)에 따라 생성된 Ba-ferrite가 합성되는 온도는 더 낮은 온도에서 생성됨을 알 수 있었다.

• 한국자기학회:학술대회 개요집
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• 한국자기학회 1994년도 춘계연구발표회 논문개요집
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• pp.50-51
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• 1994

• 한국전기전자재료학회논문지
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• 제37권3호
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• pp.292-296
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• 2024

In this study, Iron (III) oxide-hydroxide (δ-FeOOH) was successfully synthesized using hydrogen peroxide (H₂O₂) as an oxidizing agent. The synthesis of δ-FeOOH was carried out by controlling the amount of H₂O₂, and pure δ-FeOOH was successfully synthesized in ranges from 0.2 mL to 0.6 mL of H₂O₂. The size of the synthesized δ-FeOOH particles was compared by controlling the amount of oxidant H₂O₂. The average particle size of the synthesized pure δ-FeOOH particles increased from 875.1 nm to 897.2 nm as the amount of H₂O₂ was increased. The optical properties of δ-FeOOH synthesized under these specific conditions were investigated. All δ-FeOOH showed a similar trend of increasing and decreasing light absorption from 800 nm to 400 nm, although there was a slight difference in the amount of light absorption, with the largest amount of light absorption at 410 nm. The band gap energy of δ-FeOOH through the Tauc plot method was about 2.1~2.2 eV when H₂O₂ was 0.2~1.4mL. With a sufficient small particle size, simple control of that particle size, and a small band gap energy enough to absorb light in the visible spectrum, δ-FeOOH could be useful in a variety of applications, including photoelectrochemistry and battery electrodes.

• Corrosion Science and Technology
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• 제7권2호
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• pp.119-124
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• 2008

Steel is generally not corrosion resistant to water with formation of non protective rusts on its surface. Rusts are composed of iron oxides such as $Fe_3O_4$, $\alpha-$, $\beta-$, $\gamma-$and ${\delta}-FeOOH$. However, steel, particularly weathering steel containing small amounts of Cu, Ni and Cr etc., shows good corrosion resistance against rural, industrial or marine environment. Its corrosion rate is exceedingly small as compared with that of carbon steel. According to the exposure test results undertaken in outdoor environments, the atmospheric corrosion rate for weathering steel is only 1 mm for a century. Atmospheric corrosion for steels proceeds under alternate dry and wet conditions. Dry condition is encountered on steel surface on fine or cloudy days, and wet condition is on rainy or snowy days. The reason why weathering steel shows superior atmospheric corrosion resistance is due to formation of corrosion protective rusts on its surface under very thin water layer. The protective rusts are usually composed of two layer rusts; the upper layer is ${\gamma}-FeOOH$ termed as lepidocrocite, and inner layer is nano-particle ${\alpha}-FeOOH$ termed as goethite. This paper is aimed at elucidating the atmospheric corrosion mechanism for steel in comparison with corrosion in bulky water environment by use of empirical data.The summary is as follows: 1. No corrosion protective rusts are formed on steel in bulky water. 2. Atmospheric corrosion for steel is the corrosion under wetting and drying conditions. Corrosion and passivation occur alternately on steel surface. Steel, particularly weathering steel with small amounts of alloying elements such as Cu, Ni and Cr etc. enhances forming corrosion protective rusts by passivation.

• 한국세라믹학회지
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• 제19권3호
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• pp.223-228
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• 1982

For the preparation of ferroxidure BaO.5.5 $Fe_2O_3$ with high coercive force, the green and calcined coprecipitates, which were obtained by neutralizing the mixed salt solution $FeCl_2-BaCl_2$ and $FeCl_3-BaCl_2$ with alkali solution $NaOH-Na_2CO_3$, were investigated about the thermal reaction, crystal growth, and the magnetic properties of the sintered specimens. The very single-domain crystallites of Ba-ferrite with high coercive force are formed from the coprecipitate of amorphous $Fe(OH)_3$ and amorphous $BaCO_3$ at lower temperature than that of subnucleus crystalline $\delta$-FeOOH and amorphous $BaCO_3$.

• 한국환경보건학회지
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• 제21권2호
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• pp.68-74
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• 1995

The optimum conditions was synthesized for the formation of Magnetite ($Fe_3O_4$) by air bubbling with the suspensions obtained by mixing Ferrous sulfate ($FeSO_4\cdot 7H_2O$) and Sodium Hydroxide (NaOH) solution in various values equivalent ratio($R=2NaOH/FeSO_4$) were studied. The changes of the structure were measured with XRD, $EM and BET. Equivalent ratio R: 0.65 was synthesized Goethite ($\alpha$-FeOOH), which becomes Maghemite ($\gamma=Fe_2O_3$) by dehydration, reduction and oxidation process. At the equivalent ratio over 1 (R>1), Magnetite ($Fe_3O_4$) was synthesized directly. The oxygen-deficient Magnetite ($Fe_3O_{4-\delta}$), which is obtained by flowing $H_2$ gas(100 ml/min) through the synthesis Magnetite at 350$\circ$C for 4 hr. By using it, was researched the decomposition reaction of $CO_2$. $CO_2$ was decomposed nearly 100% in 45 minutes by the oxygen-deficient Magnetite.

• 한국세라믹학회지
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• 제38권11호
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• pp.1023-1029
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• 2001

육방정 페라이트 $Co_2$Z(B $a_3$ $Co_2$F $e_{24}$ $O_{41}$ )를 여러 공침-산화 방법으로 제조하여 생성과정을 연구하였으며, 적절한 제조 방법을 결정하였다. 산화 및 공침 순서를 다르게 하여 $Ba^{2+}$, $Co^{2+}$, F $e^{2+}$ 등의 염화물 혼합 수용액으로부터 $Co_2$Z 조성의 수산화물을 제조하였다. 그리고 열처리 온도에 따른 생성상의 변화를 열분석(DTA/TGA), 분말 X-선 회절분석, 주사전자현미경 등을 이용하여 관찰하였다. $Co_2$Z 상은 출발물질이 비정질에 가까운 산수산화철($\delta$-FeOOH)일 경우에만 관찰되었으며, $Ba_3$F $e_{32}$ $O_{51}$ , BaF $e_{12}$ $O_{19}$ (M형), $Ba_2$ $Co_2$F $e_{12}$ $O_{22}$ (Y형)로부터 생성되었다. 염화물 혼합 수용액을 산화시킨 다음 침전하여 합성한 공침물은 110$0^{\circ}C$부터 $Co_2$Z가 생성되었다.