• Journal of the Korean Chemical Society
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• v.42 no.2
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• pp.184-189
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• 1998

Tris(pentafluorophenyl)indium acetonitrile complexes have been prepared from the reaction of Indium trihalides (halogen=Cl, Br) and bis(pentafluorophenyl)cadmium in acetonitrile, and characterized by elementary analysis, $^13C{^1H}-,\; ^1H-\;and\; ^{19}F-NMR$ spectroscopy and mass spectrometry. The Indium (III) compounds were formed stable 1:1 adducts with acetonitrile. $In(C_6F_5)_3{\cdot}DMAP$ has been prepared from the ligand exchange reaction of In$(C_6F_5)_3 {\cdot} CH_3CN$ with DMAP in $CH_2Cl_2 {\cdot} DMAP$ has higher donating character and replaced the $CH_3CN$ through the ligand transfer reaction.

• Journal of the Korean Chemical Society
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• v.29 no.4
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• pp.372-381
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• 1985

Oxo molybdenum (V) complexes of substituted 8-quinolinols were synthesized and characterized by means of the investigation of elemental analysis, infrared spectra, electron spectra, electric conductivity and mass spectrometry compared with oxo molybdenum (VI) complexes. Oxo molybdenum(V) complexes were nonelectrolyte and one strong band of stretching mode of molybdenum and terminal oxygen appeared approximately $940cm^{-1}$. Oxo molybdenum(VI) complexes gave two peaks corresponding molybdenum containing ions, a molecular ion (I) of a 2 : 1 (ligand : metal) chelate and a fragment ion (II) of a 1:1 chelate due to the loss of ligand radical from ion (I). Molybdenum(V) complexes were observed the fragment ion(II) of a 1 : 1 chelate partly. The electronic spectra corresponding to d-d transition and charge transfer transition were observed and interpreted.

• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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• 2006.11a
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• pp.201-201
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• 2006

영구자석은 크게 Hard ferrite와 희토류계 자석, 그리고 Alnico 주조자석으로 구별되어진다. 그동안 Hard ferrite는 산업적으로 전자기 응용제품 또는 각종 구동 모터에 응용되어 왔지만, 최근 Nd계 희토류 자것이 고성능 모터의 소재로 급격히 대체되고 있다. 하지만, 희토류계 원료에 비해 동일 중량 대비 40~60배 가량 저렴한 Hard ferrite의 사용은 현재까지도 꾸준히 유지되고 있으며, 최근 자동차 고성능 모터용 Sr ferrite의 개발이 연구 중이다.[2] 본 연구에서는 제일원리 전산모사를 통하여 HCP 구조의 기본 Unit Cell 64개 원자를 가진 Sr-ferrite의 격자상수를 계산하여 기존 연구결과와 비교하였으며, 자화에너지와 자기모멘트를 계산하였다. 또한 향후 각종 첨가물의 영향에 대한 연구를 위해 기본 구조 및 치환 구조에 대해 고찰하였다. 그 결과 가장 안정한 에너지를 갖는 격자상수는 a=5.88, b=23.03으로 계산되어 Kimura et al의 측정 결과와 유사한 결과를 얻을 수 있었으며, $E_F$가 3.9171, $M_B$는 46.6481로 계산되었다. 항후 Sr-ferrite의 구조에서 Fe atom의 일부를 동일주기 원소인 Cr, Mn, Co, Ni, Cu로 치환하여 자기적 특성을 계산하여 본 연구결과와 비교하고자 한다.

• Applied Chemistry for Engineering
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• v.9 no.5
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• pp.774-780
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• 1998

For the stabilization of the spinel structured $LiMn_2O_4$, a fraction of manganese was substituted with various metals such as Mg, Fe, V, W, Cr, Mo with Mn that had a similar ionic radii ($LiM_xMn_{2-x}O_4(0.05{\leq}x{\leq}0.02)$). The $LiM_xMn_{2-x}O_4$ showed a substantial improvement as lower capacity loss than that of the spinel structured $LiMn_2O_4$ when it was used as a cathode material. And with the partial substitution, the chemical diffusion coefficient for $LiMg_{0.05}Mn_{1.9}O_4$ and $LiCr_{0.1}Mn_{1.9}O_4$ was increased by and order of magnitude compared to that of the $LiMn_2O_4$ with spinel structure. The results showed that significant improvement can be made on the electrochemical characteristics as the structure of the $LiMn_2O_4$ electrode material was stabilized by the partial substitution.

• Journal of the Korean Magnetics Society
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• v.1 no.2
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• pp.55-59
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• 1991

The temperature-dependent magnetization curves of amorphous Fe-Co-(Nd, Sm, Gd, Tb)-B alloys were measured using a vibrating sample magnetometer from 77 K up to 900 K. The spin wave stiffness constants and the range of the exchange interaction were calculated from the saturation magnetization values at 0 K. Curie temperatures and the Bloch coefficients estimated from the saturation magnetization curves. The low temperature dependence of magnetization is in good agreement with Bloch relation, $M_{s}(T)=M_{s}(O)(1-BT^{3/2}-CT^{5/2})$. The spin wave stiffness constant and the range of exchange interaction are decreased by substitution of heavy rare earth (Tb, Gd).

• Korean Chemical Engineering Research
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• v.47 no.2
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• pp.163-168
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• 2009

Negative differential resistance(NDR) behaviors of Keggin-type and Wells-Dawson-type heteropolyacids with cation, heteroatom, and polyatom substitutions were investigated by scanning tunneling microscopy. A reliable correlation between NDR peak voltage and reduction potential of heteropolyacid catalysts was established. It was found that more reducible heteropolyacid catalyst showed NDR behavior at less negative voltage, regardless of the structural difference. Thus, NDR peak voltage of heteropolyacid catalyst could be utilized as a single correlating parameter for the reduction potential of heteropolyacid catalyst.

• Journal of the Korea Academia-Industrial cooperation Society
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• v.12 no.10
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• pp.4696-4703
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• 2011

Tetraazamacrocyclic ion-exchangers, 1,4,8,11-tetraazacyclotetradecane bonded Merrifield peptide resin(TDM), 1,4,8,12-tetraazacyclopentadecane bonded Merrifield peptide resin(TPM) were prepared, and the ion-exchange capacity of these TDM and TPM were characterized. The distribution coefficients in various conc. of NH4Cl for magnesium with ion exchangers were determined by using the batch method. We found the isotope separation factors on new prepared tetraazamacrocyclic ion-exchangers bonded Merrifield peptide resin(TDM, TPM). The isotope separation of magnesium was determined by using of breakthrough method of column chromatography.

• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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• 2005.11a
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• pp.246-247
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• 2005

본 연구에서는 활성탄소의 표면 작용기와 전해액, 결합제의 분해반응을 줄여서 내구성을 향상시키기 위해 $H_2$ 기체의 Spill-Over 현상을 이용하여 활성탄소 표면의 작용기를 치환시킨 시료를 사용하여 전극을 구성하였다. $H_2$기체로 활성탄소를 700$^{\circ}C$에서 열처리한 결과, 원소 분석기 (Elemental Analyzer)를 이용한 원소 분석 시에 산소의 비율이 1.4%로 활성탄소의 2.44%에 비해 감소함을 알 수 있었고, Carbon의 비율이 700$^{\circ}C$에서 94.3%로 증가함을 알 수 있었다. 또한, 활성탄소를 사용한 전극을 1.2M TEABF$_4$/Acetonitrile 전해액을 사용하여 커패시터를 구성 했을 때, 1kHz의 AC저항은 700$^{\circ}C$에서 열처리한 활성탄소가 0.58\Omega$로 활성탄소의 1.300에 비해 양호한 전기화학 특성을 나타내었다.

• Proceedings of the Korean Nuclear Society Conference
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• 1995.05a
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• pp.668-673
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• 1995

$UO_2$-CeO$_2$ 모의혼합분말에 첨가제를 미량 첨가하여 소결체의 미세구조 변화를 $UO_2$분말의 경우와 비교, 관찰하였다. 소결 첨가제로서 Ta, Ti 및 Nb를 사용하였으며, 이들을 미세한 산화물의 형태로 $UO_2$ 및 $UO_2$-CeO$_2$에 첨가하여 환원성 및 산화성 분위기에서 각각 소결하였다. Ta, Ti 및 Nb는 환원소결에서 $UO_2$의 결정립을 성장시켰으나 산화소결에서는 첨가효과가 크게 나타나지 않았다. $UO_2$-0.lw%TiO$_2$와 $UO_2$-0.6w%Ta$_2$O$_{5}$의 환원소결체에서 eutectic phase가 관찰되었으나 산화소결체에서는 나타나지 않았다. $UO_2$-4wt%CeO$_2$의 환원소결에서는 Ti만이 결정립성장에 기여하는 것으로 나타났으며 Ta, Nb와 같이 $UO_2$에 치환형으로 고유되는 원소는 Ce 이온과 Cluster를 형성함으로 결정립성장에 거의 기여하지 못하고, Ti와 같이 UO2$_2$ 침입형으로 고용되는 원소는 일부가 인접한 Ce$_{U}$' 이온과 cluster를 형성하더라도 나머지가 V$_{U}$'의 형성에 기여하므로서 결정립을 성장시킬 수 있다.

• Journal of the Korean Chemical Society
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• v.37 no.8
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• pp.717-722
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• 1993

Reactions of [PtCl$_4$]$^{2-}$ with excess of dithiocarbamates in water lead to facile replacement of the chloro ligand by dithiocarbamato ligand to give [Pt(A)], [Pt(B)$_2$]Cl$_2$, [Pt(C)$_2$], and [Pt(D)(CH$_2$=CH$_2$)Cl]Cl. The complexes of platinum have been characterized by elemental analyses, infrared and UV-visible spectra, and conductivity measurements. Platinum(II)-dithiocarbamate complexes were soluble in polar solvents such as water, alcohol, acetone, dimethylformamide, and dimethylsulfoxide etc. The possible structure was proposed on the basis of elemental analyses and physical properties.