• 한국자기학회지
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• 제4권4호
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• pp.335-339
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• 1994

$Eu(Fe_{1-x}In_{x})O_{3}$ (x=0, 0.03과 0.05)의 결정구조와 자기적 성질을 상온에서의 X선 회절, $M\"{o}ssbauer$ 분광학 및 자기이력곡선 측정 방법에 의해서 연구하였다. X선 회절 분석 결과는 모든 시료가 orthorhombic 결정구조를 가지며, 단위포의 체적은 x=0을 제외하면 In 농도의 증가에 따라 증가함을 보인다. $M\"{o}ssbauer$ 스펙트럼은 두셋트 여섯 lines을 갖는다는 가정하에 분석하였다. 분석 결과는 각 셋트에서의 초미세 자기장은 x의 증가에 따라 감소하였다. 본 연구의 시료에서 공명 흡수선의 반폭이 x의 증 가에 따라 증가함은, 측정 data가 $Fe^{3+}$ 이온 주위 z개의 $In^{3+}$ 이온이 존재할 확률 분포, $_{n}P_{z}(x)$에 비례하는 초미세 구조에 의한 흡수선의 합으로 이루어졌음을 의미한다. 자기이력 곡선에서 $M_{s}$와 $H_{c}$는 각각 X의 증가에 따라 감소와 증가를 보인다.

• 한국문화재보존과학회:학술대회논문집
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• 한국문화재보존과학회 2004년도 제20회 발표논문집
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• pp.33-42
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• 2004

The forged iron axe found in the No. 2 wood-framed tomb (the middle 3rd century) of Hwangseongdong, Gyeongju is rectangular on the plane level. It shows an obtuse angle in the edge part, while the joint part has the both sides folded up and shows the traces of wood. Under the reflected light, the Iron axe shines in metal luster, which is bright light gray or light creamy colors. The result of x-ray diffraction analysis shows that the axe consists of magnetite and geothite, which can explain why the composition and structure of the original ore has been kept intact. The microtexture of the axe has the irregular network of ferrite and pearlite, and tile cementite of tiny amount in the ferrite background. The overall treatment of the texture seems to be thermal with a high ratio of carbon. There are fine-grained magnetite, wolframite, quartz, calcite, mica, hornblende and pyroxene inside the axe. Those must be the impurities that they failed to remove in the refining process. The normal ferrite is composed of pure iron whose $Fe_2O_3$ proportion is from 99.16 to $99.84\;wt.\%$. Other than them, the ferrite parts usually contain $Al_2O_3\;and\;SiO_2$. The irregular network of pearlite also contains Impurities including $Al_2O_3\;and\;SiO_2$ and shows highly diverse patterns of carbon content. It's because the axe was carburized after the material was made to resemble pure iron. The decarbonization work didn't go well along the process marks. It's estimated that the original ore was bloom produced in low-temperature reduction and formed around in $727^{\circ}C$, which is eutetic temperature.

• 보존과학회지
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• 제28권1호
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• pp.7-20
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• 2012

이 연구에서는 천안 쌍용동 용암유적에서 출토된 조선시대(15~17세기) 토기에 대한 재료과학적 특성과 원료의 산지를 해석하였다. 토기가마 폐기장과 공방지에서 수습한 토기시료는 회색 및 적색계열로 다양한 형태와 소성온도에 따른 굳기 차이가 있으나 대체로 유사한 기질특성을 보인다. 또한 모든 토기와 공방지 토양은 산출상태, 광물조성 및 지구화학적 거동특성이 상당히 유사하나, 유적지 주변에서 수습한 토양은 이들과 상이한 재료학적 특성을 가진다. 그러나 식질의 공방지 토양은 용암유적 조선시대 토기제작에 실제 이용된 원료점토로 판단된다. 이 용암유적 조선시대 토기 중 연질토기는 운모의 상전이 온도인 $900^{\circ}C$ 전후, 경질토기는 뮬라이트와 사장석의 생성과 소멸온도를 기준으로 $1,000{\sim}1,100^{\circ}C$의 소성온도를 경험한 것으로 해석된다.

• 한국식품과학회지
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• 제27권4호
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• pp.532-536
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• 1995

저장 중에 수분활성이 전분의 이화학적 성질에 미치는 영향을 알아보기 위해 수분활성도(0.32, 0.48, 0.75, 0.89)로 조절된 데시케이터에 고구마 전분을 넣고 $40^{\circ}C$ 항온기에서 5, 15, 30일간 저장한 다음 이화학적 특성을 비교하였다. 입자의 모양이나 형태는 변화가 없었고, 결정형은 Ca형으로 변하지 않았다. 수분활성이 높을수록, 저장기간이 길어질수록 수분함량과 물결합능력은 증가하였고, 요오드 친화력과 $80^{\circ}C$에서의 팽윤력은 감소하였다. 아밀로그라프에 의한 호화 양상은 저장 15일에는 뚜렷한 차이를 보이지 않았으나, 저장 30일에는 수분활성이 높을수록 $50^{\circ}C$ 냉각점도, consistency와 setback이 증가하였다.

• 한국식품과학회지
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• 제34권5호
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• pp.842-845
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• 2002

현미 쌀가루의 평균입경과 중심입경은 각각 $33.41\;{\mu}m$와 $11.46\;{\mu}m$, 유색미 쌀가루는 각각 $38.53{\mu}\;m$와 $15.18\;{\mu}m$로 유색미의 입경이 현미보다 더 컸다. 유색미와 현미의 물결합능력은 각각 133.19%, 112.08%로 유색미의 물결합능력이 더 높았으며 X-선 회절도에 의한 결정형은 전형적인 A형을 보였으며 상대결정도는 유색미 쌀가루와 현미 쌀가루는 각각 0.35, 0.36으로 큰 차이를 보이지 않았다. 유색미와 현미를 $20{\sim}25^{\circ}C$의 온도에서 60분 동안 침지하면서 조사한 수분흡수속도는 수침온도와 시간이 증가할수록 수분흡수량이 더 크게 나타났으며, $50^{\circ}C$에서 유색미와 현미의 수분흡수속도상수는 각각 $0.0388\;min^{-1/2}$, $0.0273\;min^{-1/2}$으로 유색미가 더 높았다.

• 약학회지
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• 제42권2호
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• pp.153-158
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• 1998

Calcium hydrogen phosphate was synthesized by reacting calcium chloride and sodium hydrogen phosphate solution in this study. It is well known that the particle size and yield o f calcium hydrogen phosphate produced is greatly affected by the synthetic conditions such as the reactant concentration, reaction temperature, reacting fine, mole ratio and drying temperature, etc. The purpose of this study is to investigate the optimum synthesis condition from the viewpoint of yield and sedimentation volume of the prepared calcium hydrogen phosphate powder according to a randomized complete block design proposed by G.E.P. Box and K.B. Wilson. It was found that the optimum synthetic conditions of calcium hydrogen phosphate were as follows: It was found that optirnum temperature range of reactant solutions was $28-38^{\circ}C$ and $32-42^{\circ}C$ respectively, on the viewpoint of yield and sedimentation volume. The optimum concentration range of reactant solutions was 5.5-10.0% and 6.9-7.4% respectively, on the viewpoint of yield and sedimentation volume. The optimum mole ratio of $CaCl_2$ to $Na_2HPO_4$ was in the range of 1.2-2.0 and the optimum reacting time range was 8.5-11.0 minutes. The optimum drying temperature range was $39-41^{\circ}C$ from the viewpoint of yield, but it was $39-43^{\circ}C$ on the basis of sedimentation volume. Crystallographic analysis to X-ray diffraction patterns of commercially available ecalcium hydrogen phosphate and calcium hydrogen phosphate samples prepared in this study suggested that all samples tested belonged to monoclinic crystal system characteristic of $CaHP0_4{\cdot}2H_20$ crystals.

• 대한전자공학회논문지SD
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• 제43권5호
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• pp.11-16
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• 2006

본 연구는 SiOC 박막의 비정질 정도와 유전상수와의 상관성에 관하여 정리하고 있다. 고밀도 플라즈마 CVD 방법에 의해 증착된 SiOC 박막은 bistrimethyl- silylmethane와 산소가 혼합된 개스 소스의 유량비를 다르게 하였다. 증착된 박막과 $400^{\circ}C$ 열처리된 박막은 XRD분석방법을 적용하여 비정질도를 유추하였다. 적량분석을 위해서 각 시료들의 회절패턴을 푸리에 해석에 의해 동경분포함수로 변환하고 비교하였다. 열처리한 박막의 비정질도는 증착한 박막에 비하여 결정도가 높았다. 유량비에 따라서 유전상수가 변하였으며, 유전상수는 열처리 후 비정질도가 가장 큰 박막에서 가장 낮게 나타났다.

• Bulletin of the Korean Chemical Society
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• 제24권1호
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• pp.49-54
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• 2003

TiO₂nanoparticles were synthesized using the metallorganic chemical vapor deposition process. Particles with and without metal ion dopants were obtained. X-ray photoelectron and energy dispersive X-ray spectroscopic measurements confirmed the stoichiometry of the TiO₂nanoparticles. X-ray diffraction patterns showed a polycrystalline anatase structure of TiO₂. Transmission electron microscopy revealed that these particles are of nanoscale dimensions. Exact particle size and size distribution analyses were carried out by dynamic light scattering. The average particle size was determined to be 22 nm. The nanosize particles provided large surface area for photocatalysis and a large number of free surface-charge carriers, which are crucial for the enhancement of photocatalytic activity. To improve the photocatalytic activity, metal ions, including transition metal ions $(Pd^{2+},\;Pt^{4+},\;Fe^{3+})$ and lanthanide ion $(Nd^{3+})$ were added to pure TiO₂nanoparticles. The effects of dopants on photocatalytic kinetics were investigated by the degradation of 2-chlorophenol under an ultraviolet light source. The results showed that the TiO₂nanoparticles with the metal ion dopants have higher photocatalytic activity than undoped TiO₂. The $Nd^{3+}$ ion of these dopant metal ions showed the highest catalytic activity. The difference in the photocatalytic activity with different dopants is related to the different ionic radii of the dopants.

• Carbon letters
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• 제8권2호
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• pp.108-114
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• 2007

In this work, activated carbon (AC) after $HNO_3$ modification was used as the support during the production of supported $TiO_2$ to increase the high deposition efficiency and the photocatalytic activity. The results of $N_2$ adsorption showed that the BET surface area of samples decreased with an increasing of the concentration of $HNO_3$ due to the penetration of $TiO_2$. From XRD data, a single crystal structure of anatase peak was observed in diffraction patterns for the AC coated with titanium complexes. From the SEM results, almost all particles were aggregated with each other at the carbon surface and AC was covered with $TiO_2$ particles in all of the samples. The EDX spectra show the presence of C, O, Ti and other elements. It was also observed a decreasing of amount of C content with increasing Ti and O content from the EDX. The results of FT-IR revealed that the modified AC contained more surface oxygen bearing groups than that of the original AC. The effect of surface acidity and basity calculated from Boehm titration method was also evaluated from correlations as a function of NaOH, $NaHCO_3$, and $Na_2CO_3$ uptake. The surface modification of AC by $HNO_3$ leads to an increase in the catalytic efficiency of AC/$TiO_2$ catalysts, and the catalytic efficiency increases with increasing of $HNO_3$ concentration.

• 한국세라믹학회지
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• 제18권3호
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• pp.192-200
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• 1981

This study deals with the low temperature ($25^{\circ}C$-$600^{\circ}C$) properties of Kaolin-Phosphate-water systems. Phosphoric acid, mono aluminum phosphate, mono ammonium phosphate, the mixture of phosphoric acid and mono aluminum phosphate, and the mixture of phosphoric acid and mono ammonium phosphate were used to characterize the M.O.R. of the systems with to quantity of phosphates, curing time, and firing temperature. Firing shrinkage, viscosity, surface tension, DTA, TGA, and X-ray diffraction patterns were also measured in order to investigated the factors of strengthening. The results of this study were summarized as follows: 1. The M.O.R. of kaolin-phosphate systems were stronger than that of Kaolin-water system at room temperature or low temperature($25^{\circ}C$-$600^{\circ}C$). Though it was increased according to the longer curing time, the higher temperature, and the more addition of phosphate, the M.O.R. were decreased in the case of 10 wt% phosphate addition in the system of phosphoric acid, mono aluminum phosphate and phosphoric acid-mono aluminum phosphate. 2. When the concentration of Phosphate was at 4 wt%, the M.O.R. of specimen cured at $25^{\circ}C$ and added to the phosphoric acid was strongest among the specimens in added to the others phosphates. Whereas, when the concentration of phosphate was above 6wt%, the M.O.R. of specimen cured at $25^{\circ}C$ and added to the phosphoric acid mono ammonium phosphate system cured at $25^{\circ}C$ was the strongest. 3. The M.O.R. of the specimen heated, in the temperature range of 15$0^{\circ}C$-1$600^{\circ}C$, and added to the mixture of phosphoric acid-mono aluminum phosphate system or phosphoric acid-mono ammonium phosphate system was stronger than that of specimen added to Phosphoric acid, mono-aluminum Phosphate or mono-ammonium phosphate alone. 4. The bonding force of phosphate binders was more closely related to surface tension than viscosity and it tended to be inversely proportional to surface tension. The bonding force after heating treatment seemed to be caused by the change of structure of phosphate according to heating.