• Journal of the Korean Ceramic Society
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• v.39 no.10
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• pp.903-906
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• 2002

Nanosized $Mn_xFe_2O_4$ powders were prepared in ethylene glycol solution under mild temperature and pressure conditions by precipitation from metal nitrates with aqueous potassium hydroxide. The average size and distribution of the synthesized $Mn_xFe_2O_4$ powders was about 20 nm and broad, respectively. The phase of synthesized particles was crystalline reacted at 200${\circ}C$ for 6h. The magnetic properties of the synthesized $Mn_xFe_2O_4$ powders were about 35-60 (emu/g) with superparamagnetic character.

• Journal of the Korean Ceramic Society
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• v.37 no.6
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• pp.559-563
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• 2000

To decompose carbon dioxide, magnetite was synthesized with 0.2M-FeSO4$.$7H2O and 0.5 M-NaOH by coprecipitation. The deoxidized magnetite was prepared from the magnetite by hydrogen reduction for 1, 1.5, 2 hr. The degree of hydrogen reduction and the decomposition rate of carbon dioxide were investigated with hydrogen reduction time. The crystal structure of the magnetite was identified spinel structute by the X-ray powder diffractions. After magnetite was reduced by hydrogen, magnetite reduced by hydrogen become new phae(${\alpha}$-Fe2O3, ${\alpha}$-Fe) and spinel type simultaneously. After decomposing of carbon dioxide at 350$^{\circ}C$, new phse(${\alpha}$-Fe2O3, ${\alpha}$-Fe) were removed and the spinel type only existed. The specific surface area of the synthesized magnetite was 46.69㎡/g. With the increase of the hydrogen reduction time, the grain size, the hydrogen reduction degree and the decomposition rate of carbon dioxide was increased.

• Journal of the Korean Ceramic Society
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• v.35 no.3
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• pp.239-244
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• 1998

Iron complexes were prepared using ferric nitrate and ethylene glycol as starting materials and the ul-trafine ${\alpha}-Fe_2O_3$ particles with the sizes smaller than 200nm were obtained by the pyrolysis of iron com-plexes at over $350^{\circ}C$ In addition the decomposition mechanism of the synthesized iron complexes was in-vestigated by differential scanning calorimeter X-ray diffractometer and IR spectrometer. Transmission electron microscopy and BET method were performed to analyze the effects of ferric nitrate contents and reaction temperatures on the size and shape of the particles.

• Proceedings of the Optical Society of Korea Conference
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• 2001.02a
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• pp.232-233
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• 2001

2차 비선형광학 물질이 높은 응용성을 갖기 위해서는 큰 2차 비선형광학 계수뿐만 아니라 넓은 파장 영역에 걸친 투명성을 가지고 있어야 한다. vinylidene fluoride(VDF)와 trifluoroethylene(TrFE)가 공중합된 f(VDf-TrFE) 공중합체는 이러한 조건을 갖추고 있는 강유전성 물질이다. 우리는 몰비율이 72：28인 P(VDF-TrFE)을 ITO기판위에 casting하고 corona 극화한 뒤, 두 개의 입력 파장(1064nm, 532nm)에 대한 2차 조화파 발생 실험을 실시하고 Herman과 Hayden의 마커무의 식을 이용하여 2차 비선형 광학 계수를 측정하였다. (중략)

• Journal of Magnetics
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• v.4 no.2
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• pp.55-59
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• 1999

In an attempt to find an effective production way of the$ Sm_2Fe_{17}N_{x-}type material, the Sm_2Fe_{17-}$type alloy with chemical composition of Sm 22.7 wt.%, Fe72.3 wt.% Nb 5.0wt.% was subjected to a HD (hydrogen decrepitation) treatment prior to a nitrogenation, and its effect on the formation of the nitride material was investigated. The nitrogenation behaviours of the alloy were investigated using a TPA(thermopiezic analysis), TMA, and DTA under nitrogen gas, and XRD. It has been found that the previous HD treatment significantly facilitated the formation of $Sm_2Fe_{17}N_{x-}$type nitride, and this was accounted for by the clean surface and the finer particle size of the powder caused by the HD treatment. It has also been found that the hydrogen atoms existing in the initial HD-treated alloy were removed almost completely during the nitrogenation. The heat output associated with the nitrogenation of the previously HD-treated alloy was found to be significantly smaller than that of the as-cast alloy.

• Journal of Magnetics
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• v.15 no.1
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• pp.21-24
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• 2010

A new synthetic method for the formation of uniform $\alpha-Fe_2O_3$ nanoparticles was reported and their magnetic properties were investigated. The sonochemical synthesis and the subsequent take-off technique resulted in spherical shaped $\alpha-Fe_2O_3$ nanoparticles with an average diameter of 60 nm. The temperature- and applied magnetic field-dependent magnetization of the $\alpha-Fe_2O_3$ nanoparticles was explained by the sum of two contributions, i.e., the Morin transition and superparamagnetism, because the critical size for superparamagnetism was within the size variation of the nanoparticles.

• Journal of the Korean Institute of Navigation
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• v.22 no.4
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• pp.69-75
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• 1998

The super wideband electromagnetic wave absorber in RF-A-PF type has been proposed, which can be used for an anechoic chamber, wall material to prevent TV ghost, etc, In this paper, $Ni_x-Mg_{0.1}-Zn_(1-x-0.1){\cdot}Fe_2O_4$ Ferrite Powder has been fabricated. Using this, then, [$Ni_x-Mg_{0.1}-Zn_(1-x-0.1){\cdot}Fe_2O_4$-Rubber composite for RF-layer in the RF-A-PF type absorber has been fabricated and its characteristics has been analyzed. As a result, it has been shown that the $Ni_x-Mg_{0.1}-Zn_(1-x-0.1){\cdot}Fe_2O_4$-Rubber composit with the quantity $_x$ of $Ni_x$ between 0.5 and 0.6 is suitable for the RF-layer in the case of which the grain size is sub-micrometer order.

• Journal of Industrial and Engineering Chemistry
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• v.68
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• pp.140-145
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• 2018

Bulky carbon layer uniformly distributed with nanoscale $Fe_2O_3$ was prepared via a direct carbonation of $Fe^{3+}$-polyacrylonitrile complexes at $700^{\circ}C$ under $N_2$ flow. The iron oxide carbon composites exhibited an excellent cycling performance for lithium storage with a reversible capacity of ${\sim}810mAh\;g^{-1}$ after 250 cycles at a current rate of $100mA\;g^{-1}$. The enhancement was mainly attributed to dual functions of bulky carbon layer which facilitated the lithium-ion diffusion and accommodated the volume changes of active $Fe_2O_3$ during charge/discharge process. Our novel chemical strategy is quite effective for scalable fabrication of high capacity lithium-storage materials.

• Journal of the Korean Crystal Growth and Crystal Technology
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• v.14 no.6
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• pp.290-297
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• 2004

The color enhancement of natural ruby produced from Mong Hsu were carried out by the heat treatment using gas diffusion. The natural ruby in this paper has a colored patch of which the color ranges from blue to a color close to black. The most favorable heat treatment conditions were as follows; range of temperature $1400~1600^{\circ}C$, duration 12 hrs, $O_2$ atmosphere. The color tone of ruby obtained under the optimum conditions was overall clear red by partial removal of colored patch. From EPMA results, part of blue or black colored patch within ruby were found to occur by charge transfer between $Fe^{2+}{\;}and{\;}Ti^{4+}$ . These results are consistent with the XRF that contents of $Fe(Fe^{2+}{\;}or{\;}Fe^{3+}$) and $Ti^{4+}$ ion to cause a blue or black colored patch after heat treatment became slightly less than with non-treated ruby. The silk formed on the surface of ruby heat treated for 12 hrs at $1700^{\circ}C$ were found to be generated by re-crystallization of rutile $TiO_2$ by XPS analysis.

• Journal of the Korean Crystal Growth and Crystal Technology
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• v.7 no.1
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• pp.167-173
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• 1997

The $ZnFe_2O_4$ powder was prepared under glycothermal conditions by precipitation from metal nitrates with aqueous potassium hydroxide. The fine powder was obtained at temperatures as low as 225 to $300^{\circ}C$. The microstructure and phase of the $ZnFe_2O_4$ powder were studied by SEM and XRD. The properties of the powder were studied as a function of various parameters (reaction temperature, reaction time, solid loading, etc). The average particle size of the $ZnFe_2O_4$ increased with increasing reaction temperature. After glycothermal treatment at $270^{\circ}C$ for 8 h, the average particle diameter of the $ZnFe_2O_4$ was about 50 nm.