• Journal of the Korean Ceramic Society
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• v.38 no.5
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• pp.461-465
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• 2001

La$_{0.7}$Ca$_{0.3}$MnO$_3$분말은 공기중에서 하소온도와 시간의 변화에 따라 각각 용액연소법과 고상반응법을 이용하여 제조되었다. 조성 및 구조 특성을 XRD와 SEM으로부터 조사하였으며 소결성은 dilatometer에 의해 조사되었다. 또한 분말 특성은 BET에 의해 조사되었고 분말의 하소온도는 TG 분석으로부터 결정되었다. 하소온도 및 시간이 증가함에 따라 La$_{0.7}$Ca$_{0.3}$MnO$_3$상의 XRD peak가 증가하였는데, 고상반응법을 이용한 경우 100$0^{\circ}C$에서 24시간 동안 하소해서야 겨우 La$_{0.7}$Ca$_{0.3}$MnO$_3$의 단상을 얻을 수 있었으나 용액연소법을 이용한 경우, $650^{\circ}C$에서 30분 동안 하소함으로써 submicron 입자크기를 갖는 단상이면서 초미세한 La$_{0.7}$Ca$_{0.3}$MnO$_3$분말을 쉽게 얻을 수 있었다. 또한 용액연소법에 의해 제조된 다결정인 La$_{0.7}$Ca$_{0.3}$MnO$_3$분말은 49.44$m^2$/g 정도의 매우 큰 비표면적을 얻을 수 있었다. 이 값은 고상반응법에 의해 제조된 분말의 비표면적 보다 매우 컸으며 이와 같으 사실로 인해 용액연소법에 의해 제조된 분말의 소결온도를 낮출 수 있었다. 분말의 소결온도를 낮출 수 있었다.

• Korean Journal of Materials Research
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• v.6 no.2
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• pp.175-181
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• 1996

Ti(i-OC3H7)와 Ba(OH)2.8H2Or 그리고 공통용매로서 2-Methoxy Ethanol을 이용하여 균일 용액을 제조하고, 이로부터 미세하고 조성비가 균일한 BaTiO3분말을 제조하였다. 이러한 졸-겔법으로 제조된 분말을 TG-DTA와 XRD 분석으로 결정화 및 상변화를 관찰하였다. 각 온도별로 하소된 분말에서 (111)쌍정의 생성여부를 TEM을 이용해 관찰한 결과, 합성된 BaTiO3 분말에서는 하소중(111)쌍정의 생성이 활발히 일어나지 않는 것으로 판단되었다. 특히(111) 쌍정판은 합성된 겔을 120$0^{\circ}C$에서 하소한 후 이를 140$0^{\circ}C$에서 소결한 경우에만 관찰할 수 있었다. 이러한 하소온도의 영향은 원료분말의 입자크기나 형상이 쌍정 생성에 큰 영향을 미침을 의미하는 것으로, 본 연구에서는 이를 근거하여 (111) 쌍정의 생성에 대해서 고찰하였다.

• Journal of the Korean Crystal Growth and Crystal Technology
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• v.13 no.2
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• pp.73-78
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• 2003

The influence of calcination temperature on the pore structure of freeze dried silica gel derived from tetraethyl orthosilicate (TEOS) was investigated using $N_2$adsorption and mercury intrusion techniques. Freeze dried material contained not only 4-6 nm sized mesopores and 6-10 $\mu\textrm{m}$ sized macropores, but minor micropores. The change of pore structure due to the increase of calcination temperature was dependant upon the degree of densification.

• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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• 2006.11a
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• pp.34-34
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• 2006

Ferrite/Varistor 이종재료 동시소성에서 소성 시 두 재료간의 서로 다른 수축률에 의한 휠 거동을 ferrite 하소온도와 sheet 제조 시 binder 함량에 따라 제어하였다. Ferrite의 하소온도를 $750^{\circ}C{\sim}900^{\circ}C$로 변화시켰을 때 하소온도가 $900^{\circ}C$ 일 때 수축률이 varistor의 수축률과 악 1%미만의 차이로 가장 유사하였다. $900^{\circ}C$에서 하소한 ferrite의 slurry 제조 시 binder의 함량을 40wt%~50wt%로 변화시키면서 sheet를 제조하여 varistor와 적층하여 $900^{\circ}C{\sim}1000^{\circ}C$에서 소결하였다. Binder 함량이 40wt%에 ferrite와 varistor를 교대로 적층된 시편에서 동시소성 시 휨을 제거할 수 있었다.

• Journal of the Korean Ceramic Society
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• v.40 no.1
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• pp.31-36
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• 2003

In this study, nano-sized NiCuZn-ferrites for the multi-layered chip inductor application were prepared by a coprecipitation method and its electromagnetic properties were analyzed. Also, the property of low temperature sintering were studied with the initial heat treatment of powder.$(Ni_{0.4-x}Cu_xZn_{0.60})_{1+w}(Fe_2O_4)_{1-w}$ (x=0.2, w=0.03) were calcined at $300^{circ}C~750^{circ}C.$ The sintered NiCuZn-ferrites at $900^{\circ}C$ showed good apparent density $4.90g/cm^3,$ and magnetic properties of initial permeability 164 and quality factor 72. As the calcination temperature increase, the grain size of NiCuZn-ferrite increased with irregular grain distribution and its magnetic properties were deteriorated.

• Korean Journal of Crystallography
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• v.3 no.1
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• pp.1-8
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• 1992

The morphology of lead titanate powders prepared by sol-gel and coprecipitation techniques was investigated as a function of firing temperature and soaking time. PbTiO3 precursor powders were derived from a mixed solution of lead nitrate and titanium tetrachloride at 40℃ to 43℃ and pH of 9.0 to 9.7, and fired at temperatures 350-1000℃ for 1-10h in air. An increase of particle size and agglomeration with increasing calcination temperature and duration could be observed. By annealing sol-gel derived powder at 700℃, the tially-formed acicular(and/or prismatic) primary particles transformed to polyhedral shape with soaking time, and further soaking caused coarsening the polyhedral particles with rounded edges. However, the morphology of the coprecipitated powders was not varied during crystallization.

• Journal of the Korean Ceramic Society
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• v.40 no.5
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• pp.441-446
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• 2003

Fine powders of ZnO were synthesized by the sol-gel method. The shape of gel powders with calcination temperatures changed into the sheet structure, the needle shape, and the spherical grain. The growth rate of grain size was slow to 700$^{\circ}C$ but high above 700$^{\circ}C$. The bigger the grain size is, the higher the degree of crystallization is. The organic element in gel powders evaporated below 300$^{\circ}C$. Temperature dependence of conductances showed the sigmoidal shape, but the temperature range of the constant conductances narrowed with the decrement of the calcination temperature of gel powders. The optimum sensing property for CO gas were observed with the specimen calcined at 500$^{\circ}C$ and degraded with the increment of calcination temperature.

• Journal of the Korean Crystal Growth and Crystal Technology
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• v.32 no.4
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• pp.128-135
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• 2022

The inside of a quartz glass crucible for semiconductor processing, called a transparent layer, is manufactured using synthetic silica powder. Bubbles existing in the transparent layer of the crucible cause a problem of reducing the quality of the crucible as well as the yield of the silicon ingot. Therefore, the main goal of the synthetic silica powder, which is the raw material of the transparent layer, is to minimize the bubble generation factor. For this purpose, in the case of synthetic silica powder, it is necessary to minimize silanol groups, carbon and pores. In this study, synthetic silica gel was prepared using the sol-gel method, and changes in carbon content and specific surface area were investigated according to calcination temperature and dwelled time in a two-stage calcination process. The first-stage calcination process was performed between 500℃ and 600℃ and the second-stage calcination process was performed between 1000℃ and 1100℃. The dwelled time was carried out from 10 minutes to a maximum of 12 hours. The carbon content of the powder calcined at 1000℃ for 1 hour was 0.0031 wt.%, and the specific surface area of the powder calcined at 1100℃ for 12 hours was 16.6 m²/g.

• Journal of the Korean Chemical Society
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• v.21 no.2
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• pp.121-124
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• 1977

A study on the formation of black iron oxide was carried in differents of Fe(III), Fe(II) ion in the aqueous solution that iron(II) sulfate was calcined under various temperature and leached in water. The results obtained was follows; (1) It was found that the sample calcined in an electric muffle furnace maintained at $500^{\circ}C$ for 1 hour and leached in water was equivalent mole (Fe(III) /Fe(II) = 1) in 20% aqueous solution. (2) When the above mentioned solution was hydrolyzed at pH range of 7 to 8 for 2 hours at $100^{\circ}C$, 93% and over of iron was recovered in the form of ${\alpha}-Fe_3O_4$ with a black colour.

• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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• 1999.05a
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• pp.137-141
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• 1999

금속 다층박막과 미세입상 합금박막에서 발견된 Giant Magnetoresistance(GMR) 현상에 고무되어 최근에는 50년대에 밝혀졌던 산화물 자기저항 재료에 관하여 새롭게 연구하고 있으며 perovskite 구조를 가지는 La$_{1-x}$ Ca/xub x/MnO$_{3}$ 박막에서 큰 자기저항을 얻었으며 이를 Colossal Magentoresistance (CMR) 이라 부른다. 본 연구에서는 La$_{1-x}$ Ca/xub x/MnO$_{3}$ 분말을 하소온도를 700-90$0^{\circ}C$로 변화시킨 고상반응법과 자발착화연소합성법(Glycine-Nitrate Process) 으로 각각 제조하였으며 비교 분석하였다. TG-DTA을 이용하여 불순물과 미반응 물질을 확인하여 적당한 하소 온도를 결정하였고 XRD를 이용하여 결정상을 분석하였다. 주사전자현미경(SEM)으로 각각 제조된 분말의 하소후 입자의 크기를 비교하였다. GNP법으로 합성한 경우가 고상반응법을 이용한 경우보다 입자의 크기가 submicron 단위로 미세하고 균질하며 고순도의 perovskite 구조를 갖는 La$_{1-x}$ Ca/xub x/MnO$_{3}$ 분말을 얻을 수 있었다.었다.