• 한국결정성장학회지
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• 제13권2호
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• pp.63-67
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• 2003

Synthesis of $PbLaTiO_{3}$ : Mn powders containing La and Mn was carried out using $PbO,\;TiO_{2},\;La_{2}O_{3}\;and\;MnO_{2}$ as starting materials by hydrothermal method. In the synthesis of single phase $PbLaTiO_{3}$ : Mn powder containing La and Mn, the optimal x value corresponding to La substitution was 0.01 which corresponds to $0.99(Pb_{1-x}La_{2x/3}TiO_{3})+0.01MnO_{2}$. The optimal conditions for the preparation of the powder synthesis were 8 M-KOH solvent of hydrothermal solvent, $270^{\circ}C$ of reaction temperature and 24 hrs of run time. It was found that the synthesized powders had spherical morphology with average particle size of 70 nm and specific surface area of $5.5\;m^{2}/g$.

• 환경위생공학
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• 제12권1호
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• pp.25-37
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• 1997

The synthesis of high purity and ultra-fine $BaTiO_{3}$ by precipitation with gaseous $NH_{3}$ as precipitator was investigated to find an alternative process to solve various problems of present wet methods. This study consisted of two parts ; synthesis of $BaTiO_{3}$ precipitation with gaseous $NH_{3}$ and test of electrical property for the $La_{2}O_{3}$ doped $BaTiO_{3}$. The proper condition for the synthesis of $BaTiO_{3}$ by precipitation with gaseous $NH_{3}$ is as follows. The pH was 9.0. $H_{2}O_{2}$ mole ratio to $TiCl_{4}$ was 10. $NH_{3}$ gas follow rate did not influence the synthesis of $BaTiO_{3}$. The calcination temperature of $BaTiO_{3}$ was $300^{\circ}C$. Also, the synthesis of $La_{2}O_{3}$-doped $BaTiO_{3}$ was tested through the wet process. Under these condition, the shape of prepared $BaTiO_{3}$ powder was spherical type and the size of that was about $0.2{\mu}m$. After the powder was pressed, this green body was sintered at the $1300^{\circ}C$. Under these conditions, the water absorptance and the density of the obtained sintered body were below 0.04 %, 5.2 g/$cm^{3}$, respectively. Also the grain size of that was about $10{\mu}m$ and it was similar to commercial product.

• 한국재료학회지
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• 제14권5호
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• pp.310-314
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• 2004

Mechanical alloying (MA) of Ti-50.0～66.7at%Si powders was carried out in a high-energy ball mill, and in situ thermal analysis was also made during MA. In order to classify the synthesis behavior of the powders with respect to at%Si, the synthesis behavior during MA was investigated by in situ thermal analysis and X-ray diffraction (XRD). In situ thermal analysis curves and XRD patterns of Ti-50.0～59.6at%Si powders showed that there were exothermic peaks during MA, indicating TiSi, $TiS_2$, and $Ti_{5}$ $Si_4$ phase formation by a rapid exothermic reaction of self-propagating high-temperature synthesis (SHS). Those of Ti-59.8～66.7 at%Si powders, however, showed that there were no peaks during MA, indicating any Ti silicide was not synthesised until MA 240 min. For Ti-50.0～59.6at%Si powders, the critical milling times for SHS increased from 34.5 min to 89.5 min and the temperature rise, $\Delta$T (=peak temperature-onset temperature) decreased form $26.2^{\circ}C$ to $17.1^{\circ}C$ as at%Si increased. The critical composition of Si for SHS reaction was found to be 59.6at% and the critical value of the negative heat of formation of Ti-59.6at%Si to be -1.48 kJ/g.

• The Korean Journal of Ceramics
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• 제4권4호
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• pp.387-393
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• 1998

The formation of titanium diboride ($TiB_2$ ) via the reduction of $TiO_2$ with boric oxide and carbon was studied in a partially reducing atmosphere of argon mixed with 4 vol.%H2. The effect of reaction time, temperature, partial pressure of nitrogen and $TiO_2/B_2_O3$ stoichiometric ratio on the reducibility of oxides has been studied. The phases formed were analysed by using X-ray rowder diffraction and scanning sosctron microscopic techniques. In this paper, we also investigated the presence of $CaC_2$ as a reducing agent on the reducibility of oxide mixtures and on the Ti-B-C-Ca-O phase equilibria. The morphology of $TiB_2$ formed in the presence of $CaC_2$ is compared with the microstructure of $TiB_2$ formed as a consequence of carbothermic reduction. The observed variation in $TiB_2$ crystals formed is also explained.

• 한국세라믹학회지
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• 제29권3호
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• pp.202-210
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• 1992

• 한국재료학회지
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• 제14권5호
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• pp.305-309
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• 2004

Mechanical alloying (MA) of Ti-25.0～37.5at%Si powders was carried out in a high-energy ball mill, and in situ thermal analysis was also made during MA. In order to classify the synthesis behavior of the powders with respect to at%Si, the synthesis behavior during MA was investigated by in situ thermal analysis and X-ray diffraction (XRD). In situ thermal analysis curves and XRD patterns of Ti-25.0～26.1at%Si powders showed that there were no peaks during MA, indicating $Ti_{5}$ $Si_3$ was synthesised by a slow reaction of solid state diffusion. Those of Ti-27.1～37.5at%Si powders, however, showed that there were exothermic peaks during MA, indicating $_Ti{5}$ $Si_3$ and$ Ti_3$Si phase formation by a rapid exothermic reaction of self-propagating high-temperature synthesis (SHS). For Ti-27.1～37.5at%Si powders, the critical milling times for SHS decreased from 38.1 to 18.5 min and the temperature rise, ΔT (= peak temperature - onset temperature) increased form $19.5^{\circ}C$ to $26.7^{\circ}C$ as at%Si increased. The critical composition of Si for SHS reaction was found to be 27.1at% and the critical value of the negative heat of formation of Ti-27.1at%Si to be -1.32 kJ/g.

• 한국세라믹학회지
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• 제37권12호
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• pp.1165-1171
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• 2000

Ti-C-Ni 혼합분말을 이용하여 SHS 공정에 의해 TiC-Ni 복합체를 제조하였으며, 리칭(leaching) 공정을 통하여 Ni을 제거함으로써 TiC 분말을 얻었다. TiC 분말의 특성분석을 위하여 XRD, SEM, TEM, AES 등을 사용하였다. 리칭 공정에 의해 얻어진 TiC 분말은 구형을 유지하고 있으며, 평균 입자크기는 0.4$\mu\textrm{m}$였다. 구형 TiC 분말을 다시 Ni 분말과 혼합하여 소결한 후 특성을 분석하였다. 140$0^{\circ}C$에서 소결하였을 때 TiC 입자는 구형에서 각진 형태로 변화하였다. 기계적 특성결과 상용 TiC 분말을 사용하였을 때보다 SHS 공정에 의해 제조된 TiC 분말을 사용하여 소결하였을 경우 파괴 인성값이 약 20% 증가하였다.

• 한국세라믹학회지
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• 제40권1호
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• pp.87-92
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• 2003

출발 물질로 TiCx(x=0.67)와 Al 분말을 사용하여 800~150$0^{\circ}C$ 온도 구간에서 상압 또는 가압 반응으로 Ti$_3$AlC$_2$를 합성하였다. 출발 물질로 TiCx(x=0.67)와 Al 분말을 사용한 반응 합성에서는 Ti-Al intermetallic compound 또는 Al-C compound와 같은 중간 형성물은 형성되지 않았으며 Ti$_3$AlC$_2$을 합성할 수 있었다. TiCx(x=0.67)와 용융 Al의 직접 반응으로 80$0^{\circ}C$에서는 Ti$_2$AlC 상이 합성되었으며, 1200~150$0^{\circ}C$ 반응온도 구간에서는 Ti$_3$AlC$_2$ 상이 우선적으로 합성되었다. 저온에서 합성된 Ti$_2$AlC 상은 고온에서 TiC와 반응으로 Ti$_3$AlC$_2$ 상으로 합성되었다. 본 연구에서는 출발 물질로 TiCx와 Al을 사용한 Ti$_3$AlC$_2$ 상의 합성기구를 제시하였다. 합성된 Ti$_3$AlC$_2$의 미세구조는 Ti$_3$AlC$_2$ 상으로 이루어진 결정립이 45~120nm크기로 적층된 구조를 갖는다.

• 한국분말재료학회지
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• 제2권2호
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• pp.149-157
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• 1995

In this study, an attempt was made to fabricate TiAl as well as its in situ composite via combustion synthesis. The processing variable of the combustion synthesis which include aluminum content and the heating rate were found to affect the combustion temperature. The combustion temperature measured, however, was lower than the melting temperature of TiAl and the reaction product were found to include incomplet reaction products. Carbon was added in order to increase the combustion temperature as well as to form in situ reinforcements. The reaction products showed homogeneous microstructures with carbide phases formed within indicating that the addition of carbon increased the combustion temperature above the melting temperature of TiAl.

• 한국가스학회지
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• 제16권6호
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• pp.143-147
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• 2012

티타니아($TiO_2$) 나노분말의 우수한 광촉매 활성은 이를 친환경 소재로서 많은 주목을 받도록 하였다. 특히, 최근 들어 이러한 $TiO_2$의 광촉매 활성을 향상시키기 위하여 $TiO_2$ 나노분말에 금속 혹은 비금속 원소를 도핑하는 방법이 널리 시도되고 있다. 화염법, 화학기상합성법, 졸-젤법, 공침법, 이온 주입법 등 다양한 방법들이 사용되고 있으며 합성법에 따라 원소들의 도핑 거동이 달라지므로 $TiO_2$의 전자구조 및 표면성질들이 합성법의 영향을 받게 되며 광촉매 활성 역시 달라진다. $TiO_2$의 광촉매 활성은 합성법 자체에 영향을 받는 것 외에 후속의 열처리에 의해서도 달라질 수 있다. 본 연구에서는 우수한 광촉매 활성을 가진 $TiO_2$ 나노분말 소재를 제조하기 위하여 화학기상합성법(chemical vapor synthesis, CVS)으로 텅스텐(W) 원소가 도핑된 $TiO_2$ 나노분말을 제조하고 물성 및 광촉매 특성을 조사하였다. 일부의 $TiO_2$ 나노분말은 $300^{\circ}C{\sim}700^{\circ}C$ 범위에서 열처리한 후 물성 및 광촉매 특성의 변화를 조사하였다.