• Korean Chemical Engineering Research
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• 제44권3호
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• pp.259-264
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• 2006

염화반응에 의한 $TaCl_5$의 제조에서 반응생성물 중 $NbCl_5$, $TiCl_4$, $FeCl_2$ 등이 주요 불순물로 존재하게 된다. $TaCl_5$와 $NbCl_5$는 증류나 수소 환원법에 의해 쉽게 분리가 되므로, 반응생성물에서 $TaCl_5/NbCl_5$ 혼합물을 99.9％ 이상 순도로 분리하기 위해 2기의 연속식 증류공정을 사용하여 light한 성분과 heavy한 성분을 제거하는 공정을 구성하였다. 본고에서는 순차배열(direct sequence)과 비 순차배열(indirect sequence)으로서의 두 분리공정에 대한 비교연구를 상용성 화학공정모사기인 Aspen Plus 13.1을 이용해서 전산모사를 수행하였다. 비교결과 순차배열이 비 순차배열에 비하여 초기 장치투자비용이나 운전비용에서 좀 더 우수한 것으로 나타났다.

• 한국표면공학회지
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• 제41권6호
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• pp.269-273
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• 2008

The etch of $(Na_{0.5}K_{0.5})NbO_3$ (NKN) thin film was performed in $BCl_3/Cl_2/Ar$ inductively coupled plasma. It was found that the 1sccm addition $BCl_3$ (5%) into $Cl_2/Ar$ plasma caused a non-monotonic behavior of the NKN etch rate. The maximum etch rate of NKN was 95.3 nm/min at $BCl_3$ (1 sccm)/$Cl_2$ (16 sccm)/Ar (4 sccm), 800 W ICP power, 1 Pa pressure and 400 W bias power. The NKN etch rate shows a monotonic behavior a s the bias power increases. The analysis of the narrow scan spectra of XPS for both a s-deposited and etched NKN films allowed one to assume ion assisted etch mechanism. The most probable reason for the maximum etch rate can be defined as a concurrence of chemical and physical etch pathways.

• 공업화학
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• 제5권5호
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• pp.862-870
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• 1994

출발물질로 $Pb(NO_3)_2$, $Mg(NO_3)_2$, $NbCl_5$를 선정하여 이들을 수용액상으로 $Pb(Mg_{1/3}Nb_{2/3})O_3$조성에 맞도록 각 수용액을 정확히 취하여 $Pb(Mg_{1/3}Nb_{2/3})O_3$ 1M용액이 되도록 조제하였다. 이 혼합용액은 상온에서 $PbCl_2$를 형성하므로 $70^{\circ}C$로 가열하여 $PbCl_2$를 용해시킨 후, 침전제 oxine을 가하여 pH 8~10에서 공침물을 얻었다. 이 침전물을 여과, 건조의 공정을 거처 $700{\sim}1000^{\circ}C$로 5시간 하소하여 $Pb(Mg_{1/3}Nb_{2/3})O_3$을 합성하였으며 합성된 분말은 평균입경이 $0.3{{\mu}m}$ 정도이고 모양은 구형이었다. 그리고 합성된 분말을 $2000Kg/cm^2$의 압력으로 성형하고, $1100{\sim}1200^{\circ}C$로 소성하여 이론밀도의 97.4%인 소결체를 얻었고 이때의 유전율은 1kHz에서 17000이고 유전손실은 상온에서 0.02%이었다.

• Bulletin of the Korean Chemical Society
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• 제28권7호
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• pp.1167-1170
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• 2007

A simple and convenient method for the addition of TMSCN to carbonyl compounds is described. NbCl5 is found to possess a strong Lewis acid property to transform carbonyl compounds smoothly to the corresponding cyanosilylether in high yields (up to 99 %) in solvent- free conditions.

• 전기화학회지
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• 제5권4호
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• pp.183-188
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• 2002

The structure of species formed in $NbCI_5-I-ethyl-3-methylimidazolium$ chloride (EMIC) room-temperature molten salt (RTMS) was examined with the Raman spectroscopic measurement and ab initio molecular orbital calculation. The equilibrium structures of $NbCl_5,\;NbCl_6^-,\;Nb_2CI_{10},\;Nb_2CI_{11}^-,\;Nb_3CI_6^-,\;NbCI_6^--EMI^+\;(in\;which\;NbCI_6^-$ anion approaches $EMI^+$ cation with strong interaction) and $Nb_2CI_{11}^--EMI^+$ were obtained with the HF/LANL2DZ level of calculation. The harmonic frequencies at each equilibrium structure were compared with Raman spectra. The harmonic frequencies of $NbCI_6^--EMI^+,\; Nb_2CI_{11}^--EMI^+,\;and\;Nb_2CI_{10}$ were in good agreement with the Raman spectra of RTMS melts. In the $NbCI_5-EMIC RTMS$, the main species were $NbCI_6^-\;and\;EMI^+$. In the $NbCl_5-EMIC$ RTMS added $NbCl_5\;over\;50mol\%$, small amount of $Nb_2CI_{11}^-\;and\; Nb_2CI_{10}$ were also formed. The structures of anions and cation in the RTMS distorted from free ions with Coulomb force.

• 대한금속재료학회지
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• 제50권2호
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• pp.183-190
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• 2012

Hydrogen was generated by the reaction of metal hydride with water. The variation of hydrogen generation with the kind of powders (milled $MgH_2$, and $MgH_2$ milled with various contents of MgO, $MgCl_2$ or $Ni+Nb_2O_5$) was investigated. $MgH_2$ powder with a hydrogen content of 6.05 wt% from Aldrich Company was used. Hydrogen is generated by the reaction of Mg as well as $MgH_2$ with water, resulting in the formation of byproduct $Mg(OH)_2$. For about 5 min of reaction time, milled $95%MgH_2+5%MgO$ has the highest hydrogen generation rate among milled $MgH_2+x%MgO$ (x=0, 5, 10, 15 and 20) samples. Milled $90%MgH_2+10%MgCl_2$ has the highest hydrogen generation rate among all the samples.

• 한국재료학회지
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• 제29권9호
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• pp.559-566
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• 2019

$Lu(Nb,Ta)O_4:Eu^{3+}$ powders are synthesized by a solid-state reaction process using LiCl and $Li_2SO_4$ fluxes. The photoluminescence (PL) excitation spectra of the synthesized powders consist of broad bands at approximately 270 nm and sharp peaks in the near ultraviolet region, which are assigned to the $Nb^{5+}-O^{2-}$ charge transfer of $[NbO_4]^{3-}$ niobates and the f-f transition of $Eu^{3+}$, respectively. The PL emission spectra exhibit red peaks assigned to the $^5D_0{\rightarrow}^7F_J$ transitions of $Eu^{3+}$. The strongest peak is obtained at 614 nm ($^5D_0{\rightarrow}^7F_2$), indicating that the $Eu^{3+}$ ions are incorporated into the $Lu^{3+}$ asymmetric sites. The addition of fluxes causes the increase in emission intensity, and $Li_2SO_4$ flux is more effective for enhancement in emission intensity than is LiCl flux. The substitution of $Ta^{5+}$ for $Nb^{5+}$ results in an increase or decrease in the emission intensity of $LuNb_{1-x}Ta_xO_4:Eu^{3+}$ powders, depending on amount and kind of flux. The findings are explained using particle morphology, modification of the $[NbO_4]^{3-}$ structure, formation of substructure of $LuTaO_4$, and change in the crystal field surrounding the $Eu^{3+}$ ions.

• Bulletin of the Korean Chemical Society
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• 제34권7호
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• pp.1951-1952
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• 2013

• Bulletin of the Korean Chemical Society
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• 제33권9호
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• pp.2851-2852
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• 2012

• Bulletin of the Korean Chemical Society
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• 제32권8호
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• pp.2525-2526
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• 2011