• Journal of the Korean Ceramic Society
• /
• v.39 no.1
• /
• pp.33-37
• /
• 2002

The phosphorescence powder, $SrA1_2O_4:Eu^{2+}$, synthesized by a Polymerized Complex Method(PCM), has been compared with that by a Solid-State Reaction(SSR), and their luminescence characteristics have been studied. The PCM powders were synthesized at $900^{\circ}C$ and the SSR powders at $1200^{\circ}C$. The size of PCM powders was about $0.1{\mu}m$ and one tenth of that of the SSR powders, which was due to the lower synthesized temperature. On the other hand, residual carbon in the PCM powders decreased with an increase in the crystallinity of host lattice, which was responsible for the non-white color of the powders. Both powders showed the maximum luminescence peaks around 520nm in the wave length at room temperature. However, the peak position for the PCM powders was shifted to a slightly lower wavelength and the value of half-width of the peak was broad comparing to that of the SSR powders, and the peak intensity decreased significantly. Such a change in the luminescence characteristics was due to the large difference in size for two types of powders and partly the residual carbon in the PCM powders.

• Journal of the Korean Crystal Growth and Crystal Technology
• /
• v.17 no.4
• /
• pp.139-144
• /
• 2007

[ $BaWO_4$ ] crystals were synthesized using bidentate ligands. The reaction parameters such as the concentration of ligand and molar ratio of $[WO_4^{2-}]/[Ba^{2+}]$ played important roles in the formation of $BaWO_4$ crystals with various morphologies. When TMEDA was used as a ligand, the microrods of $BaWO_4$ crystals with length of $15{\sim}20{\mu}m$ were formed via the self assembly of cross-like plates of 250 nm in width and $2{\sim}3{\mu}m$ in length.

• Journal of the Korean Ceramic Society
• /
• v.33 no.10
• /
• pp.1138-1146
• /
• 1996

Al2TiO5 powder was prepared by the sol-gel processing from th metal alkoxides ; aluminium sec-butoxide (Al(OC4H9)3 and tetraethyl orthotitanate (Ti(OC2H5)4) The particles of Al2TiO5 produced from alkoxides were measured to be below $1.5mutextrm{m}$ and mre than 90% weere below 1 ${\mu}{\textrm}{m}$ however those from commercial alumina and titania were over 0.5-7${\mu}{\textrm}{m}$ and only 60% were below 1${\mu}{\textrm}{m}$ and 90% were below 2.5${\mu}{\textrm}{m}$ Therefore Al2TiO5 powder produced from alkoxides had the narrower distributionin size than that produced from the commercial alumina and titania powders. The addition of mullite or Al2O3 powder to the prepared aluminum titanate inhibited the grain growth and this resulted in decreased and increase in density.

• Korean Chemical Engineering Research
• /
• v.43 no.6
• /
• pp.691-695
• /
• 2005

Zeolite membranes on various supports such as filter paper, cotton fiber, and glass fiber filter were prepared by secondary growth hydrothermal synthesis. First, zeolite NaA (${\approx}0.5{\mu}m$) and silicalite-1 (${\approx}0.2{\mu}m$) crystals were synthesized as zeolite seed crystals, and they were attached to the surfaces of the supports via chemical bonding. Zeolite NaA or silicalite-1 membranes could be synthesized on the supports coated with the seed crystals. The prepared zeolite membranes were observed by scanning electron microscope and analyzed by X-ray diffraction.

• Journal of the Korean Crystal Growth and Crystal Technology
• /
• v.5 no.1
• /
• pp.60-66
• /
• 1995

Abstract The experimental results which is the aerosols behavior and distribution of atomized zinc nitrate ($Zn(NO_3)_2$) solution (0.5 M) by ultrasonic vibrator were in accord with the computer simulations. i.e., most aerosols passing through the reactor (hot zone) moved toward the center of reactor by thermophoresis as the axis of reactor increase. Also, the distribution of aerosols concentration was high at the center of reactor as the axis increase. Among the synthesized ZnO particles, shell-like aggregates of fracture type which could not see at the center of reactor were observed at near the wall of reactor, and the particle size ($ 1.2 {\mu\textrm{m}$) of near the wall was larger than that ($0.9 {\mu\textrm{m}$) of the center.

• 한국전기화학회:학술대회논문집
• /
• 2002.07a
• /
• pp.117-122
• /
• 2002

고체산화물 연료전지의 구성요소인 양극(공기극)을 GNP와 Pechini 법을 이용하여 $(La{1-x}Sr_x)MnO_3$ 양극을 합성하여 합성한 분말의 특성과 단위전지로 사용하기 위한 조건에서의 특성을 측정하였다. GNP로 합성한 분말의 경우 직접 $(LaSr)MnO_3$ 단일 결정상을 얻을 수 있었으나, Pechini 법으로 합성한 분말의 경우는 비정질이었다. 또한 각각의 방법으로 합성한 분말의 입자형태는 구형이었고 1차상 입자크기는 GNP가 40nm, Pechini, 법으로 합성한 경우 20nm 정도의 크기를 갖고 있었다. GNP로 합성한 분말의 입자크기와 비표면적의 경우 glycine의 첨가량이 증가함에 따라 입자크기는 감소하였으나 최적 glycine 첨가량은 2.0mole 였고, 이 때 평균2차상의 입자크기는 $13.24{\mu}m$로 agglomeration 되어있었다. 최적 cathode조성은 GNP법으로 합성한 $(La_{0.9}Sr_{0.1}MnO_3$로서 가능하였고, 이 조성에서의 열팽창계수는 $9.89\times10^{-6}/^{\circ}C$이고, 전기전도도($1200^{\circ}C$에서 2시간소결)는 110 S/cm을 나타내었다.

• Proceedings of the Korean Society of Precision Engineering Conference
• /
• 2003.10a
• /
• pp.103-103
• /
• 2003

• Journal of Plant Biology
• /
• v.35 no.2
• /
• pp.107-116
• /
• 1992

The roles of RNA- and protein-synthesis and $H^{+}$ excretion in 1AA ($10\;\mu\textrm{M}$)-induced elongation were investigated using abraded hypocotyl segments of sunflower (Helianthus annuus L.). The response of elongation initiated about 13 min after IAA treatment. Removal of cuticle, acting as diffusion barrier for inhibitors, by mechanical abrasion of hypocotyl segments enhanced the effect of inhibitors markedly, but the degree of abrasion for the saturated effect of inhibition was different among inhibitors. The elongation induced by 1M was completely inhibited when cycloheximide ($10\;\mu\textrm{M}$) was applied to abraded hypocotyl segments as shortly as 4 min before the onset of the growth response (= 10 min after administration of IAA). Cordycepin ($200\;\mu\textrm{M}$) prevented completely 1AA-induced elongation when applied as shortly as 19 min before the onset of the growth response (=5 min before administration of 1AA). Vanadate (1 mM) inhibited both lAA-induced elongation and medium acidification via lAA-induced $H^{+}$ excretion to apoplast. Cycloheximide and cordycepin also prevented lAA-induced $H^{+}$ excretion strongly. However, inhibition by cycloheximide of lAA-induced elongation was not alleviated by acidifying the cell wall to pH 4.5. The results indicate that, a few minutes before the initiation of growih, protein synthesis is demanded for the initiation of 1AA-induced elongation and the $H^{+}$ excretion to cell wall, and that the H+ excretion, even though it may be necessary for elongation, does not seem to bring about acid growth simply through acidifying cell wall.l wall.

• Polymer(Korea)
• /
• v.32 no.4
• /
• pp.377-384
• /
• 2008

In this study, the microsphere silicone polymer beads were synthesized by UV irradiation and alkoxy hydrolysis. The coefficient of variation (CV) of microsphere silicone polymer beads were decreased with increasing UV intensity, reaction time. The mean particle diameter, refractive index, and pH value were $4.1{\mu}m$, 1.43 and 7.5, respectively. Also, the true and bulk specific gravity, moisture content were 1.30, and 0.40, below 2%. The mean particle diameter and CV were the lowest at 0.1 wt% hexamethyldisilazane (HMDS) and their roundnesses were $0.95{\sim}0.98{\mu}m$ values. The particle dispersion index of microsphere silicone polymer beads was 4.92 at 450 W, 90 min and the yield was increased to 11.3% at 20 wt% methyltrimethoxysilane (MTMS). The mean particle diameter was decreased with increasing the stirring rate and reaction temperature.

• Journal of the Korean Ceramic Society
• /
• v.41 no.4
• /
• pp.289-296
• /
• 2004

Whisker and short rod shaped hydroxyapatite (Ca$_{10}$(PO$_4$)$_{6}$(OH)$_2$ with stoichiometric composition (Ca/P=1.62 -1.67, molar ratio) has been synthesized by hydrolysis and hydrothermal reaction of aqueous $\alpha$-Ca$_3$(PO$_4$)$_2$($\alpha$-TCP) solution (pH 11), respectively. The shape of resultant HAp was mainly dependent on synthetic route and the microstructural development was on processing condition. In hydrolysis processing, the degree of intersection of whiskerlike particles and agglomeration in the apsis line increased with increasing reaction time. In hydrothermal synthesis, the reaction product obtained under excessive reaction time ($\geq$3 h at 20$0^{\circ}C$) was severely agglomerated without further grain growth above certain critical size (0.75 ${\mu}{\textrm}{m}$ in length, 0.3${\mu}{\textrm}{m}$ 11m in diameter).