• Journal of the Korean Ceramic Society
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• v.32 no.3
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• pp.295-304
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• 1995

Stabilization of the perovskite phase and sequence of reactions occuring during calcination were studied with solid solutions formed between Pb(Zn1/3Nb2/3)O3 and Pb(Fe1/2Nb1/2)O3. In the PZN-PFN composition of equal molar ratio, rhombohedral type pyrochlore phase (Pb2Nb2O7) and PbO-rich distorted cubic type pyrochlore phase (Pb3Nb2O8) were coexisted as intermediate phases at temperatures below 85$0^{\circ}C$, and these phases transformed to a stable cubic type pyrochlore phase, Pb3Nb4O13 solid solution and a perovskite solid solution at temperatures above 85$0^{\circ}C$. The major stable phase as increasing sintering temperatures was a perovskite phase in this binary system and prominent suppression of the pyrochlore phase was achieved by substituting Zn2+ with Fe3+ or by increasing sintering temperature. The composition containing 20mol% PZN possessed the best dielectric properties, and the dissipation factor was lower than 5% in all compositions.

• Electrical & Electronic Materials
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• v.4 no.2
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• pp.150-158
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• 1991

본 연구에서는 0.80Pb(F $e_{1}$2/N $b_{1}$2/) $O_{3}$-(0.20-x)Pb(F $e_{2}$3/ $W_{1}$3/) $O_{3-x}$Ba(C $u_{1}$2/ $W_{1}$2/) $O_{3}$ (x=0.01, 0.02, 0.03) 세라믹을 소결온도 및 시간을 각각 860~960[.deg.C], 2시간으로 하여 일반 소성법으로 제작하였다. 시편의 조성비와 소결온도에 따른 구조적, 유전적 특성을 조사하였으며 유전손실 특성의 개선을 위해 조성 0.80Pb(F $e_{1}$2/N $b_{1}$2/) $O_{3}$-0.18Pb (F $e_{2}$3/ $W_{1}$3/) $O_{3}$-0.02Ba(C $u_{1}$2/ $W_{1}$2/) $O_{3}$시편에 Mn $O_{2}$를 0~1.25[wt%]로 첨가한 후 유전특성의 변화를 관찰하였다. Mn $O_{2}$의 첨가량이 증가함에 따라 결정립의 크기와 유전상수는 점차 감소하였다. 소결밀도는 900[.deg.C]에서 소결시킨 시편의 경우 최대값을 나타내었다. Ba(C $u_{1}$2/ $W_{1}$2/) $O_{3}$의 양이 0.01에서 0.03[mol]로 증가함에 따라 상전이온도는 38[.deg.C]에서 2[.deg.C]로 감소하였다. 조성 0.80Pb(F $e_{1}$2/N $b_{1}$2/) $O_{3}$0.18Pb(F $e_{2}$3/ $W_{1}$3/) $O_{3}$-0.02Ba(C $u_{1}$2/ $W_{1}$2/) $O_{3}$에 Mn $O_{2}$가 0.25[wt%] 첨가된 시편의 20[.deg.C]에서의 유전상수는 16,700으로 최대값을 유전손실을 1.28[%]로 최소값을 나타내었다. 또한 모든 시편은 온도 및 주파수에 따라 유전상수가 완만하게 변화하는 유전이완 특성을 나타내었다.다.

• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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• 2000.11a
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• pp.291-294
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• 2000

The crystallization behavior and dc Conductivities of CuO-P$_2$O$_{5}$ -Nb$_2$O$_{5}$ -V$_2$O$_{5}$ glasses prepared by quenching on the copper plate were investigated. The conductivities of the glasses were range from 10$^{-5}$ s.$cm^{-1}$ / at room temperature, but the conductivities of the glass-ceramics were 10$^{-3}$ s.$cm^{-1}$ / increased by 10$^2$order. The crystalline product in the glass-ceramics was CuV$_2$O$_{6}$ . The linear relationship between in($\sigma$T) and T$^{-1}$ suggested that the electrical conduction in the present glass-ceramics would be due to a small polaron hopping mechanism.

• Journal of the Mineralogical Society of Korea
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• v.23 no.2
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• pp.117-124
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• 2010

The sorption of $AsO_4,\;SeO_3,\;CrO_4$ on schwertmannite and thermal analysis of sorbed samples were carried out. The results of sorption experiments showed that sorption characteristics of those three oxyanions on schwertmannite can be divided into two groups. The extent of sorption of $AsO_4$ and $SeO_3$ were 100% at up to 1 mM solution concentration, and they increased no more significantly. This can be interpreted as $AsO_4$ and $SeO_3$ substituting $SO_4$ in schwertmannite strucure by the ratio of 1 : 1. The extent of the sorption of $CrO_4$ was much lower than those of other two oxyanions. Thermal analysis was performed using two kinds of sorbed samples at 0.1 and 1.25 mM concentrations. The results of the thermal analysis showed that the samples sorbed by three different oxyanions have different thermal characteristics. The samples sorbed by $AsO_4$ showed smaller weight loss around $600^{\circ}C$ than the original loss of pure schwertmannite, and it is attributed to the substitution of $AsO_4$ for $SO_4$, which was caused by the loss of $SO_4$, than pure schwertmannite due to the substitution of $SO_4$ by $AsO_4$. It also showed additional weight loss around $600^{\circ}C$ due to the decomposition of $AsO_4$ at that temperature. The weight loss of samples sorbed by $SeO_3$ started at slightly lower temperature than that sorbed by $SO_4$ and kept that loss at wider temperature range, probably indicating that the decomposition of $SeO_3$ occurs at slightly lower temperature. However, for the samples sorbed by $CrO_4$, the weight loss caused by the decomposition of $SO_4$ was also smaller and there was no additional weight loss at higher temperature due to the thermal stability of $CrO_4$, indicating that $SO_4$ was also substituted by $CrO_4$ in schwertmannite. Sorption experiment and thermal analysis indicate that $CrO_4$ sorbs on schwertmannite by substiuting $SO_4$, but the affinity to $SO_4$ or instability of $CrO_4$ in scwertmannite structure probably prohibit perfect 1 : 1 substitution.

• The Bulletin of The Korean Astronomical Society
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• v.35 no.1
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• pp.51.2-51.2
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• 2010

We have carried out an extensive statistical analysis based on the results of simultaneous observations of SiO and $H_2O$ masers toward 166 known SiO and $H_2O$ maser sources using KVN_Yonsei radio telescope (Kim et al.2010, ApJS submitted). We investigate the distributions of the mean velocities and the intensity ratios between SiO and $H_2O$ maser emission including those between SiO v=1 and v=2,J=1-0 transitions according to type of evolved stars. We also investigate mutual relations between SiO and $H_2O$ maser properties(total flux densities and velocity structures etc.) according to stellar pulsation phases. Most of SiO masers appear around the stellar velocity (80 % within ${\pm}5km\;s^{-1}$), while $H_2O$ masers show a different characteristic compared with SiO masers (69% within ${\pm}5km\;s^{-1}$). In addition, we investigate a correlation between $SiO/H_2O$ maser emission and AKARIFIS flux density as well as the AKARI color characteristics of SiO and $H_2O$ observational results in the AKARIFIS two-color diagram.

• Journal of the Korean Ceramic Society
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• v.19 no.4
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• pp.293-299
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• 1982

The effects of $MnO_2$ and $Cr_2O_3$ on the Piezoelectrictric properties of Pb(Mg1/2W1/2)0.3 Ti0.4 Zr0.3O3 Ceramics. Electromechanical properties in the system in connection with the sintering temperature and the effects of $MnO_2$ and $Cr_2O_3$ addition. The dielectric constant of the ceramics decreased with the additions of $MnO_2$ while the additions of $Cr_2O_3$ increased the value. The Planar coupling factor (Kp) of the ceramics with 0.2wt% $MnO_2$ and with 0.2wt% $Cr_2O_3$ gave the highest value of 0.52 and 0.513 as sintered at 106$0^{\circ}C$, 108$0^{\circ}C$, respectively. The value of mechanical Q-factor were in parallel with the fired density of the ceramics. The optical micrography of the sintered bodies showed that the additions of $MnO_2$ promoted the grain growth, while the additions of $Cr_2O_3$ retarded the grain growth.

• Journal of the Korean Chemical Society
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• v.28 no.2
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• pp.102-108
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• 1984

The catalytic oxidation of CO has been investigated on $ZnCe_{1+y}O_2$ at temperatures from 300 to $500^{\circ}C$ under various P_{CO} and PO_2 conditions. The oxidation rates have been correlated with 1.5-order kinetics: first order with respect to CO and 0.5 order with respect to O2. CO appears to be absorbed essentially on the O lattice of $ZnCe_{1+y}O_2$ as a molecular species, while $O_2$ adsorbs on an O vacancy as an ionic species. The conductivity data show that CO adsorption contributes electron to the conduction band and the adsorption process of $O_2$ withdraws it from an O vacancy. The oxidation mechanism and the defect model of $ZnCe_{1+y}O_2$ are inferred at given temperature and $PO_2'$s from the agreement between the conductivities and kinetic data. It is suggested that CO absorption is the rate-controlling.

• YAKHAK HOEJI
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• v.43 no.1
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• pp.5-10
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• 1999

As one of the serial studies on the specific and indigenous plants of Mt. Chiri the constituents of aerial part from filipendula formosa (Rosaceae) were investigated. From of the MeOH extract, five flavonol glycosides, kaempferol-3-O-$\beta$-D-galactopyranoside, querecetin-3-O-$\beta$-D-galactopyranoside, quercetin-3-O-$\alpha$-Lrhamopyranosyl (1 6)-$\beta$-D-galactopyranoside, kaempferol-3-O-$\alpha$-L-rhamnopyranosyl (1 6)-$\beta$-D-galactopyranoside and quercetin-7-O-$\beta$-D-glucopyranosy-3-O-$\beta$-D-galactopyranoside were isolated by column chromatographic separation using Amberlite XAD-2 and Sephadex LH-20, and identified physicochemical evidences (IR, FAB-Mass, $^1H,{\;}^{13}C-NMR$).

• Journal of the Korean Ceramic Society
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• v.33 no.10
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• pp.1117-1123
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• 1996

• Journal of the Korean Chemical Society
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• v.29 no.3
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• pp.265-270
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• 1985

Ta$_2$O$_5$, Nb$_2$O$_5$, SnO$_2$ and ZrO$_2$ in tin-slag samples were determined by X-ray fluorescence spectrometry using the dilution parameter method and the analytical results were compared with the data obtained by standard calibration curve method. Tin-slag samples and one standard sample having very similar composition to the tin-slags were diluted with a proper diluent (La$_2$O$_3$) to the ratio of 1: 1, 1 : 2, 1 : 3 and 1 : 4. After measuring the X-ray intensities of original and diluted samples, the values of dilution parameters were calculated by using the dilution parameter equation. Without any calibration curve, the analytical results were calculated from the equation including the dilution parameter term. The results were in good agreement with the reference data by the standard calibration curve method.