• 한국대기환경학회:학술대회논문집
• /
• 한국대기환경학회 2005년도 추계학술대회 논문집
• /
• pp.265-267
• /
• 2005

• 한국결정성장학회지
• /
• 제8권3호
• /
• pp.487-492
• /
• 1998

ICP(Inductively Coupled Plasma)를 열원으로 출발용액의 농도변화 및 $TiO_2$ 첨가로 $SnO_2$와 $(Sn,Ti)O_2$미분말을 합성하였으며 SnO2 박막을 제조하였다. 각각 합성된 $SnO_2$ 미분말은 모두 tetragonal의 rutile형으로서 입자들의 평균입경은 30nm로 매우 미세하였으며, 좁은 입도분포를 나타내었다. $TiO_2$를 첨가하였을 경우 $SnO_2-TiO_2$ 미분말은 고용체를 이루었으며, 첨가량이 증가함에 따라 결정성은 감소하였다. ICP tail flame으로 fused quartz 기판을 가열하여 (101)면을 주 peak로 하는 $SnO_2$ 박막을 얻었다.

• 한국분말야금학회:학술대회논문집
• /
• 한국분말야금학회 2001년도 추계학술강연 및 발표대회
• /
• pp.14-14
• /
• 2001

• 한국분말야금학회:학술대회논문집
• /
• 한국분말야금학회 2005년도 추계학술강연 및 발표대회강연 및 발표논문 초록집
• /
• pp.37-37
• /
• 2005

• 한국대기환경학회:학술대회논문집
• /
• 한국대기환경학회 2003년도 추계학술대회 논문집
• /
• pp.199-199
• /
• 2003

During the cleanup of US Department of energy facilities, contaminated materials, toxic and hazardous radionuclides (e.g., Th, Cs, and U) and heavy metals (e.g., Cr, Hg, Pb, and Ni)-laden ultrafine particles are generated. The size of the particles is up to about 200 nm. Understanding of the production of these nanometer size particles is critical in determining the surface cleaning efficiently. (omitted)

• 한국세라믹학회지
• /
• 제33권11호
• /
• pp.1276-1284
• /
• 1996

Ultrafine calcim carbonate powders with the size of 0.05~0.1 ${\mu}{\textrm}{m}$ and the calcite phase were prepared by the nozzle spouting method which was conducted by spouting calcium hydroxide slurry in reactor filled with CO2 gas. Well dispersed ultra-fine particles were synthesized in condition of high Ca(OH)2 concentration of the slurry ( 0.5wt%) synthesized calcium carbonate powder was shown the large particle size with agglo-meration.

• 한국재료학회지
• /
• 제13권12호
• /
• pp.806-811
• /
• 2003

Ultrafine TaC powders were synthesised by spray drying using tantalum oxalate solution. The spray dried powders were spherical shape and less than 30 $\mu\textrm{m}$ in size. The powders calcined at 500 and X$700^{\circ}C$ showed amorphous structures and $Ta_2$$O_{5}$ phase was obtained by calcining at $700^{\circ}C$. The particle size and shape remains constant after calcination. The calcined spherical powders were composed of an agglomerate of primary particles under 50 nm in size. The complete formation of TaC could be achieved by heat treatment at $1050^{\circ}C$ for 6 hrs. The observed size of TaC powders by TEM was less than 200 nm.

• 한국분말재료학회지
• /
• 제16권2호
• /
• pp.98-103
• /
• 2009

The ultrafine titanium carbonitride particles ($TiC_{0.7}N_{0.3}$) below 100nm in mean size were successfully synthesized by Mg-thermal reduction process. The nanostructured sub-stoichiometric titanium carbide ($TiC_{0.7}$) particles were produced by the magnesium reduction at 1123K of gaseous $TiC_{l4}+xC_2Cl_4$ and the heat treatments in vacuum were performed for five hours to remove residual magnesium and magnesium chloride mixed with $TiC_{0.7}$. And final $TiC_{0.7}N_{0.3}$ phase was obtained by nitrification under normal $N_2$ gas at 1373K for 2 hrs. The purity of produced $TiC_{0.7}N_{0.3}$ particles was above 99.3% and the oxygen contents below 0.2 wt%. We investigated in particular the effects of the temperatures in vacuum treatment on the particle refinement of final product.

• 한국분말재료학회지
• /
• 제11권4호
• /
• pp.322-327
• /
• 2004

Ultrafine titanium carbide particles were synthesized by the reaction of liquid-magnesium and vaporized TiCl$_{4}$+C$_{x}$Cl$_{4}$(x = 1 and 2) solution. Fine titanium carbide particles with about 50 nm were successfully produced by combining Ti and C atoms released by chloride reduction of magnesium, and vacuum was then used to remove the residual phases of MgCl$_{2}$ and excess Mg. Small amounts of impurities such as O, Fe, Mg and Cl were detected in the product, but such problem can be solved by more precise process control. The lattice parameter of the product was 0.43267 nm, near the standard value. With respect to the reaction kinetics, the activation energy for the reactions of TiCl$_{4}$+C$_{2}$Cl$_{4}$and Mg was found to 69 kJ/mole, which was about half value against the use of TiCl$_{4}$+CCl$_{4}$, and such higher reactivity of the former contributed to increase the stoichiometry until the level of TiC$_{0.96}$ and decrease the free carbon content below 0.3 wt.%.

• 한국독성학회:학술대회논문집
• /
• 한국독성학회 2005년도 춘계 국제심포지엄 및 학술대회
• /
• pp.51-82
• /
• 2005

To compare the pulmonary toxicity between ultrafine colloidal silica particles (UFCSs) and fine colloidal silica particles (FCSs), mice were intratracheally instilled with 3 mg of 14-nm UFCSs and 230-nm FCSs and pathologically examined from 30 mill to 24 hr post-exposure. Histopathologically, lungs exposed to both sizes of particles showed bronchiolar degeneration and necrosis, neutrophilic inflammation in alveoli with alveolar type II cell proliferation and particle-laden alveolar macrophage accumulation. UFCSs, however, induced extensive alveolar hemorrhage compared to FCSs from 30 min onwards. UFCSs also caused more severe bronchiolar epithelial cell necrosis and neutrophil influx in alveoli than FCSs at 12 and 24 hr post-exposure. Laminin positive immunolabellings in basement membranes of bronchioles and alveoli of UFCSs treated animals was weaker than those of FCSs treated animals in all observation times. Electron microscopy demonstrated UFCSs and FCSs on bronchiolar and alveolar wall surface as well as in the cytoplasm of alveolar epithelial cells, alveolar macrophages and neutrophils. Type I alveolar epithelial cell erosion with basement membrane damage in UFCSs treated animals was more severe than those in FCSs treated animals. At 12 and 24 hr post-exposure, bronchiolar epithelia cells in UFCSs treated animals showed more intense vacuolation and necrosis compared to FCSs treated animals. These findings suggest that UFCSs has greater ability to induce lung inflammation and tissue damages than FCSs.