• Journal of the Korean Chemical Society
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• v.24 no.3
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• pp.233-238
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• 1980

It was observed that the magnetic moment for iron in $[(DPGH)_2FeO_2Fe(DPGH)_2]$, the oxygenation product of a octahedral iron(Ⅱ) complex, $[Fe(DPGH)_2(NH_3_2]$, decreases with decreasing temperature from ${\mu}$ = 3.60 B.M (Bohr Magneton) per iron at $298^{\circ}$K down to ${\mu}$ = 1.65 B.M per iron at $4.2^{\circ}K$. This observation may be explained by a weak antiferromagnetic coupling between two iron(Ⅲ) atoms of intermediate spin state (S = 3/2) in the molecule with the coupling constant $J = -l cm^{-1}$.

• Journal of the Korean Ceramic Society
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• v.36 no.11
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• pp.1156-1162
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• 1999

• Journal of the Korean Magnetics Society
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• v.2 no.1
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• pp.15-21
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• 1992

Acicular ${\gamma}-Fe_{2}O_{3}$ particles were heated at $90^{\circ}C$ in alkaline solution containing mixed solution of dyadic metal with $Co^{+2}/Fe^{+2}$ ratio of 0.5. When cobalt content was increased, the coercivity of resultant product increased linearly, and surface area decreased. The cobalt ferrite was grown epitaxially on the surface ${\gamma}-Fe_{2}O_{3}$ crystal, and the increase of coercivity was attributed to the crystalline magnetic anisotropy of the cobalt ferrite which is conform to coating layer. We can expect superior magnetic properties above normal ratio of 2. The progress of reaction has an effect on coercivity of cobalt ferrite epitaxial iron oxide. The stability of temperature and the change om standin& of $Co-{\gamma}-Fe_{2}O_{3}$ was largely influenced by the composition of coating layer.

• Journal of the Korean Ceramic Society
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• v.38 no.5
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• pp.401-404
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• 2001

Barium ferrite powders were synthesized by the coprecipitation method using iron-pickling waste acid (IPWA) and BaCl$_2$$.$2H$_2$O as raw materials. Fe$\^$2+/ ions in the IPWA, which contains both Fe$\^$2+/ and Fe$\^$3+/ ions, were oxidized into Fe$\^$3+/ ions using H$_2$O$_2$. Proper amount of BaCl$_2$$.$2H$_2$O was dissolved into the oxidized IPWA. Using NaOH, Ba$\^$2+/ and Fe$\^$3+/ ions were coprecipitated as Ba(OH)$_2$and Fe(OH)$_3$. The coprecipitated Ba(OH)$_2$and Fe(OH)$_3$were washed and dried. Barium ferrite powders were obtained by calcining the dried Ba(OH)$_2$and Fe(OH)$_3$mixture from 400$\^{C}$ to 1000$\^{C}$ with a 100$\^{C}$ interval. Barium ferrite powders were characterized by X-ray diffraction, SEM, and VSM. It was found that barium ferrite powders could be synthesized at around 630$\^{C}$. The synthesized barium ferrite powders showed hexagonal plate shapes with a fairly uniform size. The barium ferrite powder calcined at 900$\^{C}$ showed good magnetic properties, saturation magnetization of 67emu/g and maximum coercivity of 5000 Oe.

• Journal of Nuclear Fuel Cycle and Waste Technology(JNFCWT)
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• v.19 no.2
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• pp.187-196
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• 2021

Chemical equilibrium calculations for multicomponent aqueous systems involving the reductive dissolution of magnetite (Fe₃O₄) with oxalic acid (H₂C₂O₄) were performed using the HSC Chemistry® version 9. They were conducted with an aqueous solution model based on the Pitzer's approach of one molality aqueous solution. The change in the amounts and activity coefficients of species and ions involved in the reactions as well as the solution pH at equilibrium was calculated while changing the amounts of raw materials (Fe₃O₄ and H₂C₂O₄) and the system temperature from 25℃ to 125℃. In particular, the conditions under which Fe₃O₄ is completely dissolved at high temperatures were determined by varying the raw amount of H₂C₂O₄ and the temperature for a given raw amount of Fe₃O₄ fed into the aqueous solution. When the raw amount of H₂C₂O₄ added was small for a given raw amount of Fe₃O₄, no undissolved Fe₃O₄ was present in the solution and the pH of the solution increased significantly. The formation of ferrous oxalate complex (FeC₂O₄) was observed. The equilibrium amount of FeC₂O₄ decreased as the raw amount of H₂C₂O₄ increased.

• Korean Journal of Materials Research
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• v.1 no.3
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• pp.145-150
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• 1991

Crystallization and embrittlement of $Fe_{78}B_{13}Si_{9}$ amorphous alloy was investigated by differential scanning calorimetry, X-ray diffraction and transmission electron microscopy. The crystallization comprizes two exothermic processes. In the first crystallization stage, $\alpha$-(Fe, Si) dendrites are formed from the amorphous state, and in the second crystallization, $Fe_2B$ compounds are formed. An abrupt decrease of the fracture strain of the ribbon started from amorphous started annealed at about $340^{\circ}C$

• Journal of the Korean Ceramic Society
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• v.28 no.2
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• pp.93-100
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• 1991

For determination the optimum manufacturing condition Fe4N powder for magnetic recording media, we have studied the following important conditions : the effect of particle size of metal powder on the nitridation, the condition of nitridation on the formation and magnetic properties of Fe4N, and stability of Fe4N powder against temperature and change on standing. The results can be summarized as : 1) Single phase Fe4N is formed at 50v/o of ammonia concentration during the nitridation reaction, 2) Single phase Fe4N is formed above 40$0^{\circ}C$, 15min regardless of the metal powder sizes, 3) Coercivity and saturation magnetization of Fe4N powder almost constant value until 20 day-passing from preparation date.

• Corrosion Science and Technology
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• v.12 no.4
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• pp.163-170
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• 2013

In NaCl solutions acidified with $H_2SO_4$, Fe20Cr1.1N alloy showed enhanced pitting corrosion resistance than Fe20Cr alloy. An XPS analysis revealed that the passive film of Fe20Cr1.1N alloy contained higher cationfraction of Cr than that of Fe20Cr alloy, and nitrogen was incorporated into the film. In addition, it was found that the passive film of Fe20Cr1.1N alloy was thinner and had higher oxygen vacancy density than that of Fe20Cr alloy. Based on these observations, it was concluded that the chemical composition was the determining factor for the protectiveness of the passive film of Fe20Cr based alloy in dilute $H_2SO_4$ solution.

• Progress in Superconductivity and Cryogenics
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• v.16 no.3
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• pp.1-3
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• 2014

We have synthesized La doped $CaFe_2As_2$ single crystals with Sn flux in an evacuated quartz ampule. Doping and pressure effects on the magnetic and superconducting properties of the under-doped $Ca_{1-x}La_xFe_2As_2$ (x=0.08, 0.1) were studied by measuring electrical resistivity under quasi-hydrostatic pressure up to 21 kbar. Magnetic transition temperatures for all studied concentrations were sharply suppressed with slight amplitude of pressure, less than 3 kbar, while superconducting transition temperatures were robust against pressure. In this communication, we report temperature-pressure phase diagram for the La-doped $CaFe_2As_2$ single crystals.

• Electrical & Electronic Materials
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• v.6 no.2
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• pp.122-128
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• 1993

본 연구에서는 0.45Pb(Fe$_{1}$2/Nb$_{1}$2/)O$_{3}$- (0.55-xPb(Fe$_{2}$3/W$_{1}$3/)O$_{3}$ (x=0.20, 0.25, 0.30) 세라믹을 950~990[.deg.C]에서 2시간 유지시켜 일반소성법으로 제작하였다. 제작된 시편에 대해 적층 세라믹 캐패시터로의 응용가능성을 고찰하기 위해 조성비와 소결온도에 따른 구조적, 유전적 특성을 조사하였다. PMN의 첨가량이 증가할수록 결정립 크기는 감소하였으며 상전이 온도는 증가하였다. 소결밀도는 970[.deg.C]에서 소결된 0.45PFN-0.30PFW-0.25PMN 시편에서 7.86[g/cm$_{3}$]의 최대값을 나타내었다. 유전상수는 990[.deg.C]에서 소결된 0.45PFN-0.25PFW-0.30PMN 시편에서 20,751의 최대값을 나타내었으며 유전손실은 모든 조성에서 5[%]이상을 나타내었다.