• Proceedings of the Korean Powder Metallurgy Institute Conference
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• 2002.04b
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• pp.54-55
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• 2002

• Applied Chemistry for Engineering
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• v.18 no.6
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• pp.650-653
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• 2007

$SnO_2$-doped $TiO_2$ powder was obtained from tin (IV) bis(acetylacetonate) dichloride and titanium diisopropoxide bis(acetylacetonate) with quinacridone as the dye sensitizer molecule. The structural changes of the reaction mixture were monitored by fourier transform infrared (FT-IR) spectroscopy. The morphology and microstructure of gel powder were studied by field-emission scanning electron microscopy (FE-SEM) and X-ray diffractometry (XRD). The photocatalytic activity of these powders with the anatase structure was investigated by using indigo carmine solution as a test dye

• Applied Chemistry for Engineering
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• v.17 no.5
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• pp.561-564
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• 2006

$SnO_{2}$-doped anatase type $TiO_{2}$ powder was prepared by the polymerization complex route from tin(IV) bis (acetylacetonate) dichloride, titanium diisopropoxide bis (acetylacetonate) and polyethylene glycol (PEG) as a complexing agent. The structural changes of reaction mixture were monitored by fourier transform infarared (FT-IR) spectroscopy. The microstructure and morphology of gel powder were studied by field-emission scanning electron microscopy (FE-SEM) and X-ray diffractometry (XRD). The photocatalytic activity of these powders with the anatase structure was investigated by using indigo carmine solution.

• Journal of Powder Materials
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• v.28 no.1
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• pp.31-37
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• 2021

This study explores reducing the oxygen content of a commercial Ti-48Al-2Cr-2Nb powder to less than 400 ppm by deoxidation in the solid state (DOSS) using Ca vapor, and investigates the effect of Ca vapor on the surface chemical state. As the deoxidation temperature increases, the oxygen concentration of the Ti-48Al-2Cr-2Nb powder decreases, achieving a low value of 745 ppm at 1100℃. When the deoxidation time is increased to 2 h, the oxygen concentration decreases to 320ppm at 1100℃, and the oxygen reduction rate is approximately 78% compared to that of the raw material. The deoxidized Ti-48Al-2Cr-2nb powder maintains a spherical shape, but the surface shape changes slightly owing to the reaction of Ca and Al. The oxidation state of Ti and Al on the surface of the Ti-48Al-2Cr-2Nb powder corresponds to a mixture of TiO2 and Al2O3. As a result, the peaks of metallic Ti and Ti suboxide intensify as TiO2 and Al2O3 in the surface oxide layer are reduced by Ca vapor deposition.

• Journal of Powder Materials
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• v.8 no.1
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• pp.35-41
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• 2001

$BaTiO_3$ fine powder was synthesized by hydrothermal process from the mixture of titania-hydroxide($TiO_2{\cdot}xH_2O$) and barium hexa-hydroxide ($Ba(OH)_2{\cdot}8H_2O$) as starting materials. Fine powder(< 100 nm) was made under the reaction conditions of 18$0^{\circ}C$,10 atm, 1.5 hr in autoclave and showed cubic structure. The powders were sintered by a spark plasma sintering technique from 1050~115$0^{\circ}C$ for 5 min. The grains of sample sintered at 110$0^{\circ}C$ were about 0.9${\mu}m$ in average size and showed the mixture of cubic and tetragonal structures.

• Proceedings of the Korea Society for Energy Engineering kosee Conference
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• 2002.11a
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• pp.165-169
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• 2002

BaTiO$_3$ 분말을 Ba(OH)$_2$ㆍ8$H_2O$와 아나타제형의 TiO$_2$ㆍ$\chi$$H_2O$를 이용하여 광화제 첨가 없이 열수처리에 의한 탈수(dehydration) 및 재결정화(recrystallization) 과정을 통한 수열합성법에 의해 제조하였다. Autoclave 반응기를 이용한 실험의 경우, BaTiO$_3$ 분말을 생성하기 위한 최적 반응온도 및 시간은 각각 21$0^{\circ}C$, 4시간으로 확인되었으며, 이 때 생성된 BaTiO$_3$ 분말의 크기는 0.1~0.2$mu extrm{m}$로 입도분포가 양호하였다. 그리고, 바륨과 티타늄의 농도비가 증가됨에 따라 결정화도(tetragonality)가 증가하는 경향을 나타내고 있다. 이는 반응하지 않고 남아 있는 바륨의 영향으로 생각되며, 이는 반응물의 pH와도 관련이 있다. 또한, 반응온도 및 시간도 결정화도에 커다란 영향을 미치는 변수로 주로 반응온도 및 시간이 증가함에 따라 결정화도도 함께 증가하는 추세를 나타내고 있다.

• Proceedings of the Korean Powder Metallurgy Institute Conference
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• 2006.04a
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• pp.61-62
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• 2006

• Proceedings of the Korean Powder Metallurgy Institute Conference
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• 2006.04a
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• pp.64-65
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• 2006

• Proceedings of the Korean Powder Metallurgy Institute Conference
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• 1998.10b
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• pp.38-38
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• 1998

• Proceedings of the Korean Powder Metallurgy Institute Conference
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• 2005.11a
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• pp.52-52
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• 2005