• 한국세라믹학회지
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• 제29권12호
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• pp.942-948
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• 1992

Ultrafine iron oxide powder, {{{{ gamma }}-Fe2O3 and $\alpha$-Fe2O3, were prepared by the thermal decomposition of organometallic compounds. The formation process of powder includes the thermal decomposition and oxidation of the organometallic precursors, Fe(N2H3COO)2(N2H4)2 (A) and N2H5Fe(N2H3COO)3.H2O (B). The organometallic precursors, A and B, were synthesized by the reaction of ferrous ion with hydrazinocarboxylic acid, and characterized by quantitative analysis and infrared spectroscopy. The mechanistic study for the thermal decomposition was performed by DAT-TG. The iron oxide powder was obtained by the heat treatment of the precursors at 20$0^{\circ}C$ and $600^{\circ}C$ for half an hour in air. The phases of the resulting product were proved {{{{ gamma }}-Fe2O3 and $\alpha$-Fe2O3 respectively. The particle shape was equiaxial and the particle size was less than 0.1 ${\mu}{\textrm}{m}$. Magnetic properties of the {{{{ gamma }}-Fe2O3 powder obtained from A and B was 234 Oe of coercivity, 64.26 emu/g of saturation magnetization, 23.59 emu/g of remanent magnetization and 24.1 Oe, 47.27 emu/g, 3.118 emu/g respectively. The value of $\alpha$-Fe2O3 powder was 1.494 Oe, 0.4862 emu/g, 0.1832 emu/g and 1,276 Oe, 0.4854 emu/g, 0.1856 emu/g respectively.

• 한국세라믹학회지
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• 제30권4호
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• pp.279-288
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• 1993

A study on calcination and reduction of AUC(ammonium uranyl carbonate, (NH4)4UO2(CO3)3) has been carried out by using TG-DTA in N2, air and H2 atmospheres, respectively. Phases of various intermediate obtained during thermal analysis of AUC in different atmospheres were confirmed by XRD. Powder characteristics of each intermediate were investigated by measuring particle size and specific surface area, and also observed by SEM. As a results, regardless of applied atmosphere AUC was calcined into amorphous UO3, which was converted to $\alpha$-U3O8 Via $\alpha$-UO3 in both H2 and N2 atmosphere, but directly into $\alpha$-UO3 in air atmosphere. Further reduction of U3O8 was only detectable in hydrogen atmosphere. During calcination and reduction, average particle size was reduced to less than 30% of original value without morphology change. Specific surface area was dramatically increased with release of NH3, CO2 and H2O from AUC powder and reached maximum value around 25$0^{\circ}C$, and then gradually decreased with the increase of temperature due to sintering effect of uranium oxides such as UO3 and U3O8. It was also found that the change of average crystallite size and pore size were closely related to the changes of specific surface area of uranium oxides.

• Geomechanics and Engineering
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• 제12권4호
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• pp.639-655
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• 2017

The binary mixture consists of two types of granular media with different physical attributes and sizes, which can be characterized by the percentage of large granules by weight (P) and the particle size ratio (${\alpha}$). Researchers determine that two thresholds ($P_S$ and $P_L$) exist for the peak shear strength of binary mixtures, i.e., at $P{\leq}P_S$, the peak shear strength is controlled by the small granules; at $P{\leq}P_L$, the peak shear strength is controlled by the large granules; at $P_S{\leq}P{\leq}P_L$, the peak shear strength is governed by both the large and small granules. However, the thresholds of binary mixtures with different ${\alpha}$ values, and the explanation related to the inner details of binary mixtures to account for why these thresholds exist, require further confirmation. This paper considers the mechanical behavior of binary mixtures with DEM analysis. The thresholds of binary mixtures are found to be strongly related to their coordination numbers $Z_L$ for all values of ${\alpha}$, where $Z_L$ denotes the partial coordination number only between the large particles. The arrangement structure of the large particles is examined when P approaches the thresholds, and a similar arrangement structure of large particles is formed in both 2D and 3D particle systems.

• KSBB Journal
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• 제25권1호
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• pp.97-102
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• 2010

The enhancement of immunity for atopic dermatitis with application of eicosapentaenoic acid (EPA)-loaded liposome was evaluated on NC/Nga mice. The EPA-loaded liposome was coated with thiol-chitosan. The liposomes were characterized with transmission electron microscopy (TEM), surface zeta potential & particle size analyzer (Zeta-PSA) and differential scanning calorimetry (DSC). The loading efficiency of EPA in the liposome was about 4.7%. The particle size of the EPA-Ioaded liposome was about 230 nm. The values of Immunoglobulin E (IgE), interleukin-4 (IL-4), and tumor necrosis factor-$\alpha$ (TNF-$\alpha$) were reduced significantly with application of the EPA-loaded liposome. The interferon-$\gamma$ (IFN-$\gamma$) value was increased with the application effect. It is concluded that EPA loaded liposome have immunity advancing effects in mouse model of atopic dermatitis.

• 한국세라믹학회지
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• 제35권3호
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• pp.239-244
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• 1998

출발원료인 ferric nitrate와 ethylene glycol를 사용하여 iron complex를 제조하였으며 이를 $350^{\circ}C$ 이상의 온도에서 열처리하여 200nm 이하의 미세한 입자 크기를 갖는 ${\alpha}-Fe_2O_3$ 분말을 얻었다. 또한 열분석 X-선 회절 분석 및 적외선 분광 분석을 통하여 제조된 iron complex의 분해 mechanism에 대하여 조사하였고, 출발원료의 조성비 및 반응온도에 따른 입자 크기 및 형상의 변화 양상을 전자현미경 분석과 비표면적 분석을 통하여 조사하였다.

• 한국정밀공학회:학술대회논문집
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• 한국정밀공학회 2001년도 춘계학술대회 논문집
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• pp.381-384
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• 2001

The combined stirring method to uniform distribution of particle is consisted of two strring force both electro-magnetic stirring generated from induction heating and mechanical stirring with graphite stirrer. PMMC billets were fabricated with the volume fractions ranged from 0% to 20% and particle sizes ranged from 14$\mu\textrm{m}$ to 25$\mu\textrm{m}$. It is important to control the size of primary ${\alpha}$-AI solid particles because it could become the cause of the particle pushing or capture phenomena from the fact that secondary dendrite arm spacing size depends on the cooling rate during the solidification in hypoeutectic AI-Si alloy.

• 한국의학물리학회:학술대회논문집
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• 한국의학물리학회 2002년도 Proceedings
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• pp.174-176
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• 2002

A total of 134 patients with stage 1 of non-small cell lung cancer treated by carbon ion beam of HIMAC NIRS were investigated for control rate and delivered dose. The delivered dose of every patient was converted to biological effective dose (BED) of LQ model using fraction number, dose per fraction and alpha beta ratio which shows the maximum correlation between BED and tumor control. The BED of every patient was classified to establish a BED response curve for control. Assuming fraction numbers, dose response curves were introduced from BED response curve. The total doses to realize several control rates were obtained for the treatment of small fraction number.

• 멤브레인
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• 제25권1호
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• pp.15-26
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• 2015

본 연구에서는 기공의 크기가 큰 다공성 지지체를 $3{\sim}4{\mu}m$, 150 nm의 크기를 갖는 ${\alpha}$-알루미나 입자를 물과 실리카-지르코니아 용액에 각각 분산시키는 방법으로 표면 개질을 하였다. $3{\sim}4{\mu}m$ 크기의 알루미나 입자가 분산된 용액을 이용하여 금속 지지체 및 알루미나 지지체에 코팅하였을 때, 코팅횟수가 증가할수록 지지체의 표면의 큰 기공이 감소하였고, 여기에 150 nm 크기의 알루미나 입자가 분산된 용액으로 추가 코팅을 하면 작은 크기의 알루미나 입자가 기공 사이사이에 들어가면서 지지체를 좀 더 매끄럽게 개질하는 역할을 하는 것을 확인하였다. 특히 실리카-지르코니아 용액을 분산매로 하여 표면 개질을 한 경우, 알루미나 입자가 실리카-지르코니아 층에 촘촘하게 박힌 모양으로 고정이 되어 지지체 개질에 효과적임을 확인하였다. 이러한 방법으로 제조된 실리카-지르코니아 분리막의 기체투과도는 상온에서 각각 $1.8-8.4{\times}10^{-4}mol{\cdot}m^{-2}{\cdot}s^{-1}{\cdot}Pa^{-1}$, $3.3-5.0{\times}10^{-5}mol{\cdot}m^{-2}{\cdot}s^{-1}{\cdot}Pa^{-1}$이며 수소/질소 선택도는 Knudsen 분포를 보였다. 표면 개질된 지지체에 다양한 분리층을 형성하는 방법으로 무기 분리막 응용에 이용할 수 있을 것으로 예상된다.

• Journal of Radiation Protection and Research
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• 제2권1호
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• pp.1-8
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• 1977

중성자(中性子) 선량(線量) 측정목적(測定目的)으로 사용(使用)할 Posi필름 고체비적검출기(固體飛跡檢出器)의 알파입자(粒子) 비적검출(飛跡檢出) 효율(效率)과 화학부식(化學腐蝕)에 의(依)한 그의 비적형성(飛跡形成) 최적조건(最適條件)을 실험적(實驗的)으로 결정(決定)하였다. $^{10}B$ 및 $^{27}Al$박(箔)과 posi 필름 고체비적검출기(固體飛跡檢出器)로 이루어진 중성자(中性子) 선량계(線量計)를 제작(製作)하고 이것에 의(依)한 중성자(中性子) 선속밀도(線束密度) 및 선량(線量)의 측정범위등(測定範圍等)을 실험결과(實驗結果)와 이론적(理論的)인 근거하(根據下)에서 산출(算出)하였다. 그 결과(結果) posi 필름 고체비적검출기(固體飛跡檢出器)는 핵분열성(核分裂性) 물질(物質)을 입자방출체(粒子放出體)로 병용(倂用)함이 없이 중성자(中性子) 측정(測定)에 효과적(效果的)으로 응용(應用)될 수 있음이 판명(判明)되었다.

• 한국재료학회지
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• 제27권4호
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• pp.179-183
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• 2017

$2ZrO_2{\cdot}P_2O_5$ powder, which is not synthesized by solid reaction method, was successfully synthesized through PVA solution method. In this process, the firing temperature and the PVA content strongly affected the crystallization behavior and final particle size. A stable ${\alpha}$-phase $2ZrO_2{\cdot}P_2O_5$ was synthesized at a firing temperature of $1200^{\circ}C$ and holding time of 4 h. ${\beta}$-phase $2ZrO_2{\cdot}P_2O_5$ was observed, with un-reacted $ZrO_2$ phases, for firing temperatures lower than $1200^{\circ}C$. In terms of the PVA content effect, the powder prepared with a PVA mixing ratio of 12:1 showed stable ${\alpha}$-phase $2ZrO_2{\cdot}P_2O_5$; however, the ${\beta}$-phase was found to co-exist at relatively higher PVA content. The synthesized ${\alpha}$-phase $2ZrO_2{\cdot}P_2O_5$ powder showed an average particle size of 100~250 nm and an average thermal expansion coefficient of $-2.5{\times}10^{-6}/^{\circ}C$ in the range of room temp. ${\sim}800^{\circ}C$.