• Journal of the Korean Ceramic Society
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• v.28 no.7
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• pp.517-524
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• 1991

The CVD process of BPSG (BoroPhosphoSilicate Glass) and its thin film properties were studied. B2H6, PH3, SiH4 and O2 gases were reacted in a AP (Atmospheric Pressure) CVD system in the temperature range of 300℃ and 460℃. The interaction of B2H6 and PH3 was studied from the deposition rate and dopant incorporation change point of view. The dependency of BPSG step coverage on the temperature was changed with different O2/(B2H6+PH3+SiH4) ratio. Finally, the boundary which distinguishes the stable BPSG's from the ones that react with Di (Deionized) water or cleaning chemicals such as H2SO4, HCl, H2O2, NH4OH etc could be defined.

• Bulletin of the Korean Chemical Society
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• v.2 no.2
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• pp.37-41
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• 1981

The elution behaviors of molybdate and tungstate through anion exchange column have been investigated in the various concentration of hydrochloric and perchloric acid. A discussion is made to evaluate the existing these equilibrium and constant according to acidity. In both acids of 0.01-2.0 M concentration range, the existing equilibrium for molybdate and its constant calculated at $20^{\circ}C$ is $10^{18.9}$ for $Mo_8O_2^{4-} + 20H^+ {\rightleftharpoons} 8MoO_2^{2+} + 10H_2O$. In the 3-3.5 M hydrochloric acid it is 0.16 for $MoO_2Cl_2 + Cl^- {\rightleftharpoons} MoO_2Cl^{3-}$ and for the case of tungstate, in the both acids of 0.01-1.0 M concentration range $10^{6.6}$ for $W_{12}O_{39}^{6-} + 6H^+ {\rightleftharpoons} 12WO_3{\cdot}3H_2O$. In higher concentration than 1.0 M both acids the following equilibrium seems to be existed. $12WO_3{\cdot}3H_2O {\rightleftharpoons} 12WO_3 + 3H_2O$

• The Korean Journal of Ceramics
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• v.6 no.1
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• pp.43-46
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• 2000

$H_4Nb_6/O_{17}$/CdS nanocomposites which intercalated CdS particles, less than 0.8nm thickness, in the interlayer of $H_4Nb_6/O_{17}$ were prepared by the successive ion exchange reactions of $H_4Nb_6/O_{17}$ with $Cd^{2+}$ and $C_3H_7NH_3_+$, followed by the reaction with $H_2S$ gas. $H_4Nb_6/O_{17}$/CdS photocatalytically reduced $NO_3$￣ to $NO_2$￣ and $NH_3$in the presence of sacrificial hole acceptor such as methanol under visible light irradiation (wavelength>400nm), although unsupported CdS showed no noticeable photocatalytic activity for $NO_3$￣ reduction. The catalytic activity of $H_4Nb_6/O_{17}$/CdS greatly enhanced with co-doping of Pt particles in the interlayer.

• Bulletin of the Korean Chemical Society
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• v.21 no.6
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• pp.638-640
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• 2000

• Journal of the Korean Chemical Society
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• v.45 no.6
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• pp.520-523
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• 2001

Hydrogen $peroxide(H_2O_2)$ reacts with HCr$O^-_4$ in an acidic condition to produce $CrO(O_2)_2$ which exhibits an intense blue color. This reaction is coupled with a technique of Flow Injection Analysis(FIA) for the absorption spectrometry of $H_2O_2$ in the aqueous samples. The method could be applied for the deter-mination of $H_2O_2$ over the range of 2.00{\times}$10^{-6}$M∼0.020 M with the limit of detection of ∼1.00${\times}10^{-6}$M. The method was also used to successfully determination of the $H_2O_2$ content in the snow and rain samples.

• Journal of the Korean Vacuum Society
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• v.13 no.4
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• pp.139-144
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• 2004

Recently, the importance of clean vacuum and partial pressure measurement of gas species has been increased in the vaccum process. In this study, the partial pressures of $H_2$, He, C, N, $O_2$, $H_2O $, Ar/2, $N_2$(CO), Ar, $CO_2$ were measured by residual gas analyzer according to temperature of cryogenic pump which is used to clean vacuum generation and compared. The experimental results showed that the cryopanel temperature was reached to 12K after 72 minutes of pumping and after 25hours, the partial pressures in percent were 24.9 %, 6.6%, 5.5 %, 2.2 %, 3.8%, 30.7%, 6.5%, 6.1 %, 5.5%, 8.2% for $H_2$, He, C, N, $O_2$, $H_2O $, Ar/2, $N_2$, Ar, $CO_2$ respectively. The dominant gases were $H_2$ and $H_2O $, and the partial pressures were relatively high compare to other gases.

• Journal of Korean Society for Atmospheric Environment
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• v.13 no.5
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• pp.397-410
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• 1997

An annular denuder filter pack sampling system (ADS) was used to collect acidic air pollutants in Pusan. During the study period (from June 1995 to November 1995), forty eight samples were collected every 12 hours starting from 6:00 in the morning. These samples were devided into two sets of data for day (6:00 a.m.-6:00 p.m.) and night (6:00 p.m.-6:00 a.m.). The chemical species were analyzed for HN $O_3$, HN $O_2$, S $O_2$ and N $H_3$ in the gas Phase, and N $O_3$$^{[-10]}$ , S $O_4$$^{2-}$ and N $H_4$$^{+}$ in the particulate phase. The mean concentrations measured from this study were 0.24, 1.91, 30.07 and 4.24 $\mu\textrm{g}$/㎥ for HN $O_3$, HN $O_2$, S $O_2$ and N $H_3$, respectively. The mean concentrations of N $O_3$$^{[-10]}$ , S $O_4$$^{2-}$ and N $H_4$$^+{\ulcorner}$ were 1.95, 7.36 and 3.48 $\mu\textrm{g}$/㎥, respectively. The mean concentrations of gaseous species except for HN $O_2$ were higher in daytime than in nighttime, but the reverse was true in the particulates except for N $H_4$$^{+}$. +/..

• Journal of Electrical Engineering and Technology
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• v.10 no.4
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• pp.1786-1795
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• 2015

It is common practice to identify the insulation faults of GIS through monitor the contents of SF₆ decomposed components. Partial discharges (PD) could lead to the decomposition of SF₆ dielectric, so new reactions usually occur in the mixture of the newly decomposed components including traces of H₂O and O₂. The new reactions also cause the decomposed components to differ due to the different amounts of H₂O and O₂ even under the same strength of PD. Thus, the accuracy of assessing the insulation faults is definitely influenced when using the concentration and corresponding change of decomposed components. In the present research, a needle-plate electrode was employed to simulate the PD event of a metal protrusion insulation fault for two main characteristic components SO₂F₂ and SOF₂, and to carry out influence analysis of trace H₂O and O₂ on the characteristic components. The research shows that trace H₂O has the capability of catching an F atom, which inhibits low-sulfide SF_x from recombining into high-sulfide SF₆. Thus, the amount of SOF₂ strongly correlates to the amount of trace H₂O, whereas the amount of SO₂F₂ is weakly related to trace H₂O. Furthermore, the dilution effect of trace O₂ on SOF₂ obviously exceeds that of SO₂F₂.

• Journal of the Society of Cosmetic Scientists of Korea
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• v.34 no.3
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• pp.157-165
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• 2008

In the previous study, the anti-oxidant activity of oxtract/fraction of Sueada aspparagoides(SA) and the stability test for the cream containing SA extract were investigated respectively[1,2]. In this study, the components of SA extract were analyzed by TLC, HPLC, and LC/ESI-MS/MS, $^1H$-NMR. TLC chromatogram of ethyl acetate fraction of SA extract revealed 5 bands $(SA1{\sim}SA5)$. HPLC chromatogram of aglycone fractions obtained from deglycoylation reaction of ethyl acetate fraction showed 2 bands (SAA 2 and SAA 1), which were identified as quercetin (composition ratio, 16.88%) and kaempferol (83.12%) in the order of elution time. Among 5 bands of TLC chromatogram, 4 bands $(SA2{\sim}SA5)$ also were Identified as kaempferol-3-O-glucoside (SA 2), quercetin-3-O-glucoside (SA3), kaempferol-3-O-rutinoside (SA 4), quercetin-3-O-rutinoside (SA 5) by LC/ESI-MS/MSMS/MS. respectively. The spectrum generated for SAA 1 by LC/ESI-MS/MS in the negative ion mode also gave the ion corresponding to the deprotonated aglycone $[M-H]^-$ (285m/z), the $^1H$-NMR spectrum contained signals [${\delta}$ 6.19 (1H, d, J=1.8Hz, H-6), ${\delta}$ 6.44 (1H, d, J=1.8Hz, H-8), ${\delta}$ 6.92 (2H, d, J=9.0Hz, H-3', 5'), ${\delta}$ 8.04 (2H, d, J=9.0Hz, H-2', 6', thus SAA 1 was identified as kaempferol. SAA 2 yielded the deprotonated agycone ion $[M-H]^-$ (301m/z), $^1H$-NMR spectrum showed signals [${\delta}$ 6.20 (1H, d, J=2.0Hz, H-6), ${\delta}$ 6.42 (1H, d, J=2.0Hz, H-8), ${\delta}$ 6.90 (1H, d, J=8.6Hz, H-5'), ${\delta}$ 7.55 (1H, dd, J=8.6, 2.2Hz, H-6'), ${\delta}$ 7.69 (1H, d, J=2.2Hz, H-2', thus SAA 2 was Identified as quercetin. In conclusion, with the anti-oxidant activity and the stability test reported previously, component analysis of SA extracts could be applicable to new cosmeceuticals.

• Journal of the Korean Ceramic Society
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• v.27 no.7
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• pp.899-906
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• 1990

The cordierite powders were prepared from Mg(NO3)2.6H2O, Al(NO3)3.9H2O and colloidal silica by the coprecippitation method, and the sintering behavior of the powders were investigated. Two different methods were applied for producing the precursor powders. The one was to added the aqueous solution of Mg(NO3)2.6H2O and Al(NO3)3.9H2O to NH4OH to adjust pH at 10 where the colloidal silica of pH 10 was added. The other wa to add the aqueous solution of Mg(NO3)2.6H2O and Al(NO3)3.9H2O to the colloidal silica with NH4OH to control the final mixture to be at pH 10. It was confirmed that more homogeneous powders were obtained from the latter method. The firing linear shrinkage of the powder compacts fabricated from the calcined powder between 90$0^{\circ}C$ and 110$0^{\circ}C$ was found to be larger as the calcination temperature was low. But all of them stopped shrinking around 120$0^{\circ}C$. The powder compacts, fabricated using the calcined powders at 90$0^{\circ}C$ and 95$0^{\circ}C$ for 2hours and sintered at 142$0^{\circ}C$ for 2hours, showed relative density of 93-96%, 3-point bending strength of 81-83MPa, KIC of 1.9-2.4 MPam1/2 and thermal expansion coefficient of 0.213-0.732$\times$10-6$^{\circ}C$.