• 한국환경과학회지
• /
• 제22권1호
• /
• pp.83-89
• /
• 2013

Silicon carbide with aluminium oxide was used to remove the sulphur hexafluoride ($SF_6$) gas using microwave irradiation. The destruction and removal efficiencies (DREs) of $SF_6$ were studies as a function of various decomposition temperatures and microwave powers. The decomposition of $SF_6$ gas was analyzed using GC-TCD. XRD (X-ray powder diffraction) and XRF (X-ray Fluorescence Spectrometer) were used to characterize the properties of aluminum oxide. DREs of $SF_6$ were increased as the microwave powers were increased. Additive aluminium oxide on SiC increased the removal efficiencies and decreased the decomposition temperature. The XRD results show that the ${\gamma}-Al_2O_3$ was transformed to ${\alpha}-Al_2O_3$ during $SF_6$ decomposition by microwave irradiation. It was found that the best material to control $SF_6$ was SiC with $Al_2O_3$ 30 wt% in consideration of microwave energy consumption and $SF_6$ decomposition rate.

• 한국산학기술학회논문지
• /
• 제8권5호
• /
• pp.995-999
• /
• 2007

저온 소결용 압전 세라믹 소결체의 치밀화에 미치는 첨가제의 영향을 조사하기 위하여 $PbZrTiO_3$(PZT) 분말을 제조하였으며, 이 PZT 분말을 이용하여 제조한 압전 세라믹스의 치밀화에 미치는 첨가제의 영향을 조사하였다. 첨가제는 $wB_2O_3-xBi_2O_3-zCuO$와 $LiBiO_2-CuO$ 두 종류가 제조되었으며 이 들 첨가제의 양을 변화 시켜 효과를 조사하였다. PZT 분말에 소결조제로서 1wt.% 의 $LiBiO_2-CuO$를 첨가하여 시편을 제조한 후, $800{\sim}1200^{\circ}C$까지의 온도 범위에서에서 소결한 결과 $900^{\circ}C$에서 최고의 소결밀도를 나타내었다. 소결된 압전체의 결정상을 분석하기 위하여 X-선회절분석을 시행하였으며, $900^{\circ}C$의 저온에서 소결한 $PbZrTiO_3$의 시편의 미세조직을 관찰하기 위하여 주사전자현미경(SEM)을 이용하였다. X-선 회절분석에서는 잘 발달된 PZT 상이 나타났으며, SEM 관찰 결과 평균입경은 $2{\sim}4\;{\mu}m$의 페로브스카이트 결정으로 균일하고 치밀한 조직을 나타내었으며, 높은 소결성은 첨가제에 의한 액상소결에 기인한다.

• 한국재료학회지
• /
• 제2권4호
• /
• pp.263-269
• /
• 1992

본 실험에서는 낮은 음의 온도계수를 갖는 저온 소결 유전체에 대해 연구하였다. 새로 개발된 재료의 조성은 Ti$O_2$(100-X) CuOx(X=1~5wt%)에 미량의 Mn$O_2$를 첨가 하였다. CuO를 첨가하지 않은 경우에는 저온 (90$0^{\circ}C$) 에서 소결이 진행되지 않았다. CuO 함량이 증가할수록 저온에서 소결이 가능하였으나, 유전율이 낮아지고 유전손실은 증가 하였다. Mn$O_2$를 0.6wt% 첨가한 경우 유전율과 Q값이 가장 높게 나타났다.

• 한국안광학회지
• /
• 제6권2호
• /
• pp.111-114
• /
• 2001

본 논문은 탄화규소와 탄화티탄으로 보강된 안경렌즈 절삭용 재료에 대한 파괴인성 및 경도에 대한 연구 결과이다. 이 재료는 $1800^{\circ}C$에서 일축 가압소결 하고, $1910^{\circ}C$에서 3시간 열처리하였다. 분당 $15^{\circ}C$씩 온도를 올렸으며, 분당 $25^{\circ}C$씩 온도를 내렸다. 안경렌즈 절삭용 재료의 입자들은 주사전자현미경을 통해 관찰하였고, 각각의 조성은 X선 회절을 통해 관찰하였다. 본 연구에서 연구된 안경렌즈 절삭용 시편의 대표적인 파괴인성과 경도는 각각 $6.1MPa{\cdot}m^{1/2}$과 15.3 GPa이었다.

• 대한전기학회:학술대회논문집
• /
• 대한전기학회 1991년도 하계학술대회 논문집
• /
• pp.204-208
• /
• 1991

In this paper, the radiation properties of a far-Infrared using a PTC thermistor, the $BaTiO_3$+1.63mol% $Al_2O_3$+3.75mol% $SiO_2$+1.25mol% $TiO_2$(1/3 $Al_2O_3+xSiO_2$+(1-x) $TiO_2$; total x: 6.67mol%) ceramics, in order to progress the grade resistivity characteristics, by adding an ethanol solution of $Mn(NO_3){\cdot}6H_2O$ was investigated. The ceramics was fabricated by wet-mill method. The sintering temperature read 1300-1350$[^{\circ}C]$ and the holding time was 3 hours. The quantity of $Sb_2O_3$ and $Al_2O_3$ for an activation of the far-infrared radiation in ceramics was doped. In sintering, R-T property was measured by varying the grade temperature. The anatase-lighting apparatus and microstructures by using XRD and SEM were observed. $Sb_2O_3$. oxides additive. affected the semiconducting and emissivity and MnO was devoted an increase of resistivity. The specimen which only $Sb_2O_3$ is added to was high appeared far-infrared emissivity and Mno was not affacted the far-infrared radiation. The ceramics shows that it is effective in the structure of the human bodies as organic bodies and can be applied as electron device.

• 한국세라믹학회지
• /
• 제39권4호
• /
• pp.352-358
• /
• 2002

고체산화물 연료전지의 전해질로서 $LaGaO_3$계를 선정하여 La 대신 Sr을, Ga 대신에 Mg를 치환하여 첨가할 때 첨가량 및 소결 조건에 따라 전해질을 제조하고, 그 특성을 조사하였다. Sr과 Mg가 0.15와 0.20 mole 첨가되었을 때 Sr과 Mg가 La와Ga 자리에 동시 고용되어 (La$_{1-x}Sr_x)(Ga_{1-y}Mg_y)O_{3-\delta}$ 단일상이 나타났고, 일부 조성에서는 $LaSrGa_3O_7$ 상과 $LaSrGaO_4$ 상이 2차상으로 나타났다. $LaSrGa_3O_7$ 상은 Sr과 Mg 첨가에 의한 상이며, $LaSrGaO_4$ 상은 액상형성에 의한 것으로 나타났으며, 또한 $LaSrGaO_4$ 상은 소결온도와 Mg 첨가량이 감소함에 따라 얻어졌다. $(La_{0.8}Sr_{0.2})(Ga_{0.8}Mg_{0.2})O_{3-\delta}$ 상의 경우 소결온도를 증가함에 따라 열팽창계수는 감소하였으며, $1500^{circ}C$에서 1시간 소결한 소결체의 전기전도도는 $800^{circ}C$, 1mA에서 0.14S/cm를 나타내었다.

• Transactions on Electrical and Electronic Materials
• /
• 제1권2호
• /
• pp.28-31
• /
• 2000

BaTiO$_3$cerameic thin films doped with Mn were manufactured by rf/dc magnetron sputter technique. We have investigated crystal structure, surface morphology and PRCR(positive-temperature coefficient of resistance) characteristics of the specimen depending on second heat-treatment temperature. Second heat treatment of the specimen were performed in the temperature range of 400 to 1350$\^{C}$ X-ray diffraction patterns of BaTiO$_3$ thin films show that the specimen heat treated below 600$\^{C}$ is an amorphous phase and the one heat treated above 1100$\^{C}$ forms a poly-crystallization . In this specimen heat-treated at 1300$\^{C}$, a lattice constant ratio(c/a) was 1.188. Scanning electron microscope(SEM) image of BaTiO$_3$ thin films of the specimen heat treated in between 900 and 1100$\^{C}$ shows a grain growth. At 1100$\^{C}$, the specimen stops grain-growing and becomes a poly-crystallization . A resistivity-temperature characteristics of the specimen depends on the doping concentrations of Mn. A resistivity ratio between the value at room temperature and the one above Curie temperature was 10$^4$ for pure BaTiO$_3$ thin films and 10$\^$5/ fo BaTiO$_3$ : additive 0.127mol% MnO

• 한국세라믹학회지
• /
• 제40권10호
• /
• pp.991-997
• /
• 2003

SiC세라믹스의 열전변환물성에 미치는 A1$_4$C$_3$ 첨가효과에 대해 연구하였다. $\alpha$-SiC 분말에 A1$_4$C$_3$를 첨가하여 Ar분위기 2100∼220$0^{\circ}C$에서 3시간 소결하여 상대밀도 47∼59%인 다공질 SiC세라믹스를 제조하였다. X-선 회절분석 및 주사형 전자현미경으로 소결체의 상조성과 미세구조를 분석하였으며, A1$_4$C$_3$ 첨가에 의해 6H에서 4H로의 상전이 발생을 관찰할 수 있었다. 전기전도도와 Seebeck 계수를 Ar 분위기 550∼95$0^{\circ}C$에서 측정하였다. 무첨가 시료의 경우 출발원료중에 함유된 p형 불순물(Al, Fe)에 의해 Seebeck 계수가 정(+)의 값을 나타내었으며, 소결온도가 증가함에 따라 전기전도도가 증가하였다. A1$_4$C$_3$ 첨가 시료의 전기전도도는 상전이 및 캐리어농도 증가에 의해 무첨가 시료보다 높았으며, 또 Seebeck 계수도 크게 나타났다. 시료의 밀도, 첨가량 및 소결조건이 열전변환물성에 크게 기여하였다.

• Bulletin of the Korean Chemical Society
• /
• 제32권8호
• /
• pp.2637-2642
• /
• 2011

A new ultrasonic-assisted micellar extraction and cloud-point pre-concentration method was developed for the determination of major saikosaponins, namely saikosaponins -A, -C and -D, in Radix Bupleuri by high performance liquid chromatography with evaporative light scattering detection (HPLC-ELSD). The non-ionic surfactant Genapol X-080 (oligoethylene glycol monoalkyl ether) was chosen as the extraction additive and parameters affecting the extraction efficiency were optimized. The highest yield was obtained with 10% (w/v) Genapol X-080, a liquid/solid ratio of 200:1 (mL/g) and ultrasonic-assisted extraction for 40 min. In addition, the optimum cloud-point pre-concentration was reached with 10% sodium sulfate and equilibration at $60^{\circ}C$ for 30 min. Separation was achieved on an Ascentis Express C18 column (100 ${\times}$ 4.6 mm i.d., 2.7 ${\mu}M$) using a binary mobile phase composed of 0.1% acetic acid and acetonitrile. Saikosaponins were detected by ELSD, which was operated at a $50^{\circ}C$ drift tube temperature and 3.0 bar nebulizer gas ($N_2$) pressure. The water-based solvent modified with Genapol X-080 showed better extraction efficiency compared to that of the conventional solvent methanol. Recovery of saikosaponins ranged from 93.1 to 101.9%. An environmentally-friendly extraction method was successfully applied to extract and enrich major saikosaponins in Radix Bupleuri.

• 한국재료학회지
• /
• 제21권8호
• /
• pp.468-475
• /
• 2011

[ $LaMeO_3$ ](Me = Cr, Co) powders were prepared using the polymeric precursor method. The effects of the chelating agent and the polymeric additive on the synthesis of the $LaMeO_3$ perovskite were studied. The samples were synthesized using ethylene glycol (EG) as the solvent, acetyl acetone (AcAc) as the chelating agent, and polyvinylpyrrolidone (PVP) as the polymer additive. The thermal decomposition behavior of the precursor powder was characterized using a thermal analysis (TG-DTA). The crystallization and particle sizes of the $LaMeO_3$ powders were investigated via powder X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), and particle size analyzer, respectively. The as-prepared precursor primarily has $LaMeO_3$ at the optimum condition, i.e. for a molar ratio of both metal-source (a : a) : EG (80a : 80a) : AcAc (8a) inclusive of 1 wt% PVP. When the as-prepared precursor was calcined at $700^{\circ}C$, only a single phase was observed to correspond with the orthorhombic structure of $LaCrO_3$ and the rhombohedral structure of $LaCoO_3$. A solid-electrolyte impedance-metric sensor device composed of $Li_{1.5}Al_{0.5}Ti_{1.5}(PO_4)_3$ as a transducer and $LaMeO_3$ as a receptor has been systematically investigated for the detection of NOx in the range of 20 to 250 ppm at $400^{\circ}C$. The sensor responses were able to divide the component between resistance and capacitance. The impedance-metric sensor for the NO showed higher sensitivity compared with $NO_2$. The responses of the impedance-metric sensor device showed dependence on each value of the NOx concentration.