• 한국세라믹학회지
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• 제14권3호
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• pp.163-168
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• 1977

As a wet chemical drying process "hot petroleum drying method" was applied and developed for preparing uniformly fine oxide powder with high purity and sinterreactivity. Using this method solution of sulfates was dried in hot petroleum bath (~17$0^{\circ}C$) to sulfate powder from which corresponding mullite doped by Fe3+ ion was formed. Particle size, shape, decomposition by heat, and phase identification of sulfate andoxide powders determined by DTA, TGA, X-ray diffraction, analysis and electron microscopy: sulfate powder prepared by this drying method is an intimate mixture of the amorphous form of uniformly and finely distributed spherical particles (0.05-0.1$\mu$). Mullitization with the sulfate powder occurs at 110$0^{\circ}C$ in air. The morphology of mullite particle made by firing the sulfate powder at 135$0^{\circ}C$ in oxygen atmosphere is granular of 0.1-0.3$\mu$ in size. This drying process proved to be a very effective method for preparing fine, homogeneous, and highly sinterreactive multicomponent oxide powder without conventional ceramic process of mixing, milling, and granulating. This process can be also applied for preparing electronic ceramic materials which are requisite for high purity and homogeneity.mogeneity.

• 한국세라믹학회지
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• 제48권1호
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• pp.1-5
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• 2011

Silicon carbide (SiC) has recently drawn an enormous industrial interest because of its useful mechanical properties such as thermal resistance, abrasion resistance and thermal conductivity at high temperature. RF Thermal plasma (PL-35 Induction Plasma, Tekna CO., Canada) has been utilized for synthesis of high purity SiC powder from cheap inorganic solution (Tetraethyl Orthosilicate, TEOS). It is found that the powders by thermal plasma consist of SiC with free carbon and amorphous silica ($SiO_2$) and, by thermal treatment and HF treatment, the impurities are driven off resulting high purity SiC nano-powder. The synthesized SiC powder lies below 30 nm and its properties such microstructure, phase composition, specific surface area and free carbon content have been characterized by X-ay diffraction (XRD), field emission scanning electron microscopy (FE-SEM), thermogravimetric (TG) and Brunauer-Emmett-Teller (BET).

• 대한전자공학회:학술대회논문집
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• 대한전자공학회 2001년도 The 6th International Symposium of East Asian Resources Recycling Technology
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• pp.719-724
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• 2001

The objective of this investigation was to separate silicon and silica for recycling by the liquid-liquid separation technique. In the preparation of silicon (Si) single crystal, a small amount of silicon is fixed on the surface of silica (quartz, $SiO_2$) crucible. The used crucible is crushed for recycling both silicon and silica in a high purity from the mixed powder. Zeta-potential of silicon and silica are almost the same at pH higher than 3. Their separation by simple flotation is ruled out. However, their hydrophobic characteristics are different in several different organic solvent from the measurement of contact angle. Therefore, the liquid-liquid extraction is employed to separate silicon and silica. The result indicates that the organic solvent mixed with dodecyl ammonium acetate could extracted the silicon powder at high purity (97-100%) with high recovery from the silica powder in the water phase.

• 분석과학
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• 제5권3호
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• pp.333-338
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• 1992

녹차 중 탄닌성분들인 에피갈로카테킨, 에피갈로카테킨 갈레이트는 세파덱스 LH-20 컬럼에서 물-아세톤의 혼합용리에 의하여 신속하게 분리되어 용출하였다. 용출액은 280nm에서 흡광도의 변화를 측정한 결과 4개의 분획으로 검출되었다. 각 분획을 그대로 고속원자충격 질량분석장치에 도입하여 탄닌성분들을 동정할 수 있었다. 에피갈로카테킨, 에피갈로카테민 갈레이트는 역상 HPLC에서 용출된 피크면적으로 계산한 결과, 70% 이상의 높은 수율로 얻을 수 있었다. 본 방법에 의하여 보고된 방법들보다 탄닌성분들을 신속하게 동정할 수 있고, 고순도로 얻을 수 있었다.

• 한국세라믹학회지
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• 제49권6호
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• pp.523-527
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• 2012

Silicon carbide (SiC) has recently drawn an enormous amount of industrial interest due to its useful mechanical properties, such as its thermal resistance, abrasion resistance and thermal conductivity at high temperatures. In this study, RF thermal plasma (PL-35 Induction Plasma, Tekna CO., Canada) was utilized for the synthesis of high-purity SiC powder from an organic precursor (hexamethyldisilazane, vinyltrimethoxysilane). It was found that the SiC powders obtained by the RF thermal plasma treatment included free carbon and amorphous silica ($SiO_2$). The SiC powders were further purified by a thermal treatment and a HF treatment, resulting in high-purity SiC nano-powder. The particle diameter of the synthesized SiC powder was less than 30 nm. Detailed properties of the microstructure, phase composition, and free carbon content were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), a thermogravimetric (TG) analysis, according to the and Brunauer-Emmett-Teller (BET) specific surface area from N2 isotherms at 77 K.

• 자원리싸이클링
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• 제28권1호
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• pp.15-22
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• 2019

습식법으로 고순도 알루미나를 제조할 수 있는 알콕사이드 가수분해법, 암모늄 명반의 열분해법, 암모늄 알루미늄탄산염(AACH) 열분해법을 소개하였다. 상기 세 공정으로 알루미나 제조시 용액의 pH, 온도와 불순물이 알루미나의 상전이와 고순도에 미치는 영향을 조사했다. 알콕사이드와 암모늄 명반의 열분해법으로는 ${\alpha}$와 ${\gamma}$알루미나의 제조가 가능하다. 그러나 AACH 열분해법으로는 ${\gamma}$알루미나 제조는 어렵다.

• 분석과학
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• 제36권4호
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• pp.143-151
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• 2023

Considering the greater role of α-amino acids in our daily lives, the enantiomer resolution of seven α-amino acids derivatized with fluorogenic reagent (4-fluoro-7-nitro-2,1,3-benzoxadiazole, NBD-F) by chiral HPLC on amylose or cellulose trisphenylcarbamate derived chiral stationary phases (CSPs) under simultaneous ultraviolet (UV) and fluorescence (FL) detection was performed. The degree of enantioseparation and resolution was affected by nature and selector backbones of the CSPs as well as the kind of amino acids. Baseline enantiomer separation and resolutions were observed for the enantiomers of all analytes as NBD derivatives especially on coated type amylose tris(3,5-dimethylphenylcarbamate) derived CSPs (Chiralpak AD-H and Lux Amylose-1). The other CSPs also showed good enantioselectivity except for the CSPs (Chiralpak IB, Chiralcel OD-H and Lux Cellulose-1) having cellulose tris(3,5-dimethylphenylcarbamate) as chiral selectors. The developed analytical chiral method was applied to determine the enantiomeric purity of seven commercially available L-α-amino acids and the impurities as D-forms were found to be in the range 0.08-0.87 %, respectively. The intra- and interday accuracy and precision assays showed high accuracy and precision of the developed analytical method. This chiral HPLC method for the enantiomer resolution of amino acids using fluorescent derivatization could be useful for the determination of enantiomeric purity of pharmaceuticals and biological study for amino acid type compounds among chiral drugs.

• 한국통신학회논문지
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• 제26권10B호
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• pp.1464-1469
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• 2001

본 논문에서는 디지털 하이브리드 위상고정루프(Digital Hybrid Phase-Locked Loop, DHPLL) 주파수 합성기 구조에서 고 순도 스펙트럼과 초고속 스위칭 속도를 위한 설계기술을 제안한다. D/A 변환기 출력으로 전압제어발진기(Voltage Controlled Oscillator, VCO)를 구동하는 개 루프(open-loop) 구성 방식과 기존 위상고정루프(Phase Locked Loop, PLL)의 폐 루프(closed-loop) 구성 방식을 혼합한 하이브리드 구조의 주파수 합성기를 고려하여, 시스템 변수(개 루프 대역과 위상 여유)와 성능 파라미터(정착시간, 위상 잡음, 그리고 최대 오버슈트(Max. overshoot)의 관계를 연구하였다. 그리고 이 관계를 통해 스펙트럼 순도와 스위칭 속도를 향상시키기 위한 최적의 3가지 설계방안을 제시한다. 컴퓨터 시뮬레이션 결과, 주파수 스위칭 과정에서 발생하는 최대 오버슈트가 0.0991%이고 완전 정상상태 도달시간은 0.288msec이다. offset 주파수 10KHz에서 위상 잡음은 -128.15dBc이다.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 1996년도 춘계학술대회 논문집
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• pp.72-75
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• 1996

A hydride vapor phase epitaxy (HVPE) method is performed to prepare the GaN thin films on c-plane sapphire substrate. The full-width at half maximum of double crystal X-ray rocking curves from 20$\mu\textrm{m}$-thick GaN was 576 arcsecond. The photoluminescence spectrum measured 10 K shows the hallow bound exciton (I$_2$) line and weak donor-acceptor peak, however, there was not observed deep donor-acceptor pair recombination indicate the GaN crystals prepared in this study are of high purity and high crystalline quality. The GaN layer is n-type conducting with electron mobility of 72 $\textrm{cm}^2$/V$.$sec and with carrier concentration of 6 x 10$\^$18/cm/sup-3/.

• Journal of Applied Biological Chemistry
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• 제55권1호
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• pp.61-65
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• 2012

Three major curcuminoids in turmeric (Curcuma longa), curcumin, demethoxycurcumin, and bisdemethoxycurcumin, were efficiently extracted by optimizing extraction condition and simultaneously analyzed and identified using reverse phase high-performance liquid chromatography, thin-layer chromatography, and liquid chromatography-mass spectrometry method. The highest yield of extraction amount 0.279 g, 9.30% was obtained by dipping method with extraction time of 7 h.