• 대한전자공학회:학술대회논문집
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• 대한전자공학회 1998년도 하계종합학술대회논문집
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• pp.449-452
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• 1998

We have studied the oxidatio nrte of $Si_{1-x}Ge_{x}$ epitaxial layer grown by MBE(molecular beam epitaxy). Oxidation were performed at 700.deg. C, 800.deg. C, 900.deg. C, and 1000.deg. C. After the oxidation, the results of AES(auger electron spectroscopy) showed that Ge was completely rejected out of the oxide and pile up at $SiO_{2}/$Si_{1-x}Ge_{x}$ interface. It is shown that the presence of Ge at the $SiO_{2}$/$Si_{1-x}Ge_{x}$ interface changes the dry oxidation rate. The dry oxidation rate was equal to that of pure Si regardless of Ge mole fraction at 700.deg. C and 800.deg.C, while it was decreased at both 900.deg. C and 1000.deg.C as the Ge mole fraction was increased. The ry oxidation rates were reduced for heavy Ge concentration, and large oxidation time. In the parabolic growth region of $Si_{1-x}Ge_{x}$ oxidation, The parabolic rate constant are decreased due to the presence of Ge-rich layer. After the longer oxidation at the 1000.deg.C, AES showed that Ge peak distribution at the $SiO_{2}$/$Si_{1-x}Ge_{x}$ interface reduced by interdiffusion of silicon and germanium.

• 대한화학회지
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• 제10권2호
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• pp.76-90
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• 1966

Ammonium sulfate synthesized by the air oxidation methods without catalyst using the reaction vessel which was fitted with fritted glass at the bottom of it and introducing, through the bottom, ammonia and air with constant flow rates to sulfurous acid solution of constant concentrations at the given temperatures. The experiment showed that the oxidation process was accelerated in accord with the increase of the air flow rates when the ammonia flow rate was constantly kept at ca. 100ml/min. in high temperatures. When the pH of the solution reached 9.0, the oxidation was nearly completed. It is assumed that in the process of reaction, $[O_{2}{\to}HSO_{3}^-]^{\neq}$ would be produced as an activated complex and the reaction was thought to be first order. The experiment indicated that the 0.5M sulfurous solution could be oxidized up to 98.54% at the flow rates of ammonia and air, 100ml/min., and 4l/min., respectively at $50^{\circ}C$.

• 한국식품위생안전성학회지
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• 제9권4호
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• pp.199-203
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• 1994

The oxidation of cholesterol in tallow heated at three frying temperatures, 130, 150 and 18$0^{\circ}C$ was studied by assaying cholesterol oxidation products(COP)by GC-MS. The correlation between levels of COP and changes of physicochemical parameters (peroxide value, polymer, polar components and dielectric constant) in tallow heated were studied. As temperature increased, the amount of cholesterol was decreased proportionally with heating time. However, the levels of COP did not increase considerably with increased frying temperature. The rate of cholesterol disappearance was the greatest at 18$0^{\circ}C$ and the smallest at 13$0^{\circ}C$. Larger amounts of COP formed were found at 15$0^{\circ}C$ than at 18$0^{\circ}C$. The levels of COP formed in tallow heated showed highly correlation with(r=0.94, n=30, p<0.01) polymer, polar components and dielectric constant, respectively.

• 환경위생공학
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• 제17권1호
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• pp.69-74
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• 2002

This study explored for treatment processes by investigating the treatment efficiency and reaction mechanism through oxidation reaction using UV and $O_3$ as oxidant in compensate the wastewater containing nitrobenzene that is non biodegradable organic. Also by modeling these reactions, we try to step explanation of optimum reaction rate and reaction mechanism as the development of the computer program predictable the reaction rate by modeling the reaction. By using this model, after kinetic constant for each reaction from an experimental data is made an optimization and for hardly contribute to reaction rate in reaction kinetic equation is made an ignorance and suppose the simplified reaction mechanism, examined the propriety of computer simulation model and simplified reaction mechanism by comparing and inspecting the reaction kinetic constant and masstransfer coefficient. An investigation results for destructional treatment of nitrobenzene in the wastewater as non-biddegradable organic using UV, $O_3{\;}O_2{\;}H_2O_2-UV$ as oxidant.

• 한국결정성장학회지
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• 제6권2호
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• pp.185-193
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• 1996

(100) Si wafer를 $2.5^{\circ},\;5^{\circ}$ 기울인 뒤, dry $O_{2}$ 분위기에서 산화시킴으로써, 시편들 간의 산화 거동 및 산화에 의한 적층 결함 특성의 차이를 알아보았다. 시편을 $900~1200^{\circ}C$에서 산화시키고 ellipsometer로 두께를 측정한 결과 저탈각 (100) Si이 (100) Si보다 산화 속도가 빨랐으며, $5^{\circ}$ off면이 $2.5^{\circ}$ off면보다 더 빨랐다. 결정방향에 따른 산화속도 차이는 산화 온도가 높아질수록 줄어들었다. 각 시편의 속도 상수에 대한 활성화 에너지는 포물 성장 속도 상수의 경우 (100) Si, $2.5^{\circ}$ off (100) Si, $5^{\circ}$ off Si이 각각 27.3, 25.9, 27.6 kcal/mol이였고, 선형 성장 속도 상수는 58.6, 56.6, 57.4 kcal/mol이였다. 또한, 두 시편에 대해 산화막을 선택 식각하 고 광학 현미경으로 관찰하여, (100) Si에 비해 $5^{\circ}$ off된 면의 산화에 의한 적층 결함 밀도가 훨씬 낮음을 확인하였고, 적층 결함 간의 각도가 달라짐을 확인하였다.

• 한국자동차공학회논문집
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• 제19권3호
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• pp.52-56
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• 2011

Active regeneration in CDPF requires $O_2$ which regenerates soot at high temperature. However, small amount of NO can interrupt $O_2$ regeneration in CDPF. To verify this phenomena, soot oxidation experiments using a flow reactor with a $Pr/CeO_2$ catalyst are carried out to simulate Catalyzed Diesel Particulate Filter (CDPF) phenomena. Catalytic soot oxidation with and without small amount of NO is conducted under tight contact condition. As the heating rate rises, the temperature gap of maximum reaction rate is increased between with and without 50ppm NO. To accelerate the $NO_2$ de-coupling effect, CTO process is performed to eliminate interfacial contact for that time. As CTO process is extended, temperature which indicates peak reaction rate increases. From this result, it is found that small amount of NO can affect tight contact soot oxidation by removal of interfacial contact between soot and catalyst.

• 한국식품과학회지
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• 제29권6호
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• pp.1094-1100
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• 1997

본 연구는 옥수수 전분을 sodium hypochlorite(NaOCl)로 산화시킬 때 산화제의 농도, pH와 온도가 미치는 영향에 대하여 조사하였다. 전분의 산화 반응은 NaOCl 농도, pH와 온도의 영향을 받았다. 산화반응은 산화제가 3.0% active Cl/g starch 이하의 농도에서는 1차 반응, 3.75% active Cl/g starch이상의 농도에서는 2차 반응으로 나타났다. 1차 반응에서 산화제의 농도가 2.25% active Cl/g starch 까지는 반응속도 상수가 증가하였고, 그 이후의 농도에서는 일정한 값을 보였다. 산화에 따른 전분내 카르복실기 함량은 반응 초기에 급격히 증가하다가 반응이 진행되면서 증가정도가 완만해졌으며, NaOCl 농도가 증가함에 따라 카르복실기의 생성량도 증가하였다. 동일한 NaOCl 농도(1.5% active Cl/g starch)에서 전분의 산화는 pH 7에서 가장 빠르게 진행되었다 온도에 따른 전분의 산화속도를 1차식으로 해석한 결과, 온도가 증가됨에 따라 속도 상수(k)값이 증가되어 반응속도가 빨라지는 것을 알 수 있었다. 한편 Arrhenius 식으로부터 산화 반응의 활성화 에너지를 계산하였을 때 1차반응의 활성화 에너지는 약 13.45 kcal/mol이었다.

• 대한환경공학회지
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• 제31권10호
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• pp.831-838
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• 2009

본 연구에서는 염소, 오존 및 오존/과산화수소 산화공정에서의 의약물질 3종의 제거특성을 살펴본 결과 diclofenac과 naproxen은 쉽게 산화공정에서 제거가 가능한 것으로 나타난 반면 ibuprofen의 경우는 산화공정에서 제거가 어려운 것으로 나타났다. 오존 단독공정 보다는 오존/과산화수소 산화공정에서의 의약물질의 제거효율이 높았으며, $H_2O_2/O_3$ 비가 1 이상에서는 제거율의 상승이 둔화되었다. 염소, 오존 및 오존/과산화수소 투입농도별 의약물질 3종에 대한 산화분해 속도 상수와 반감기를 살펴본 결과 염소, 오존 단독 투입에 비하여 오존/과산화수소 공정에서의 산화분해 속도상수가 높게 나타났고, 반감기는 단축되었다.

• 한국전기전자재료학회논문지
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• 제18권12호
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• pp.1080-1086
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• 2005

We have studied the Ge redistribution after dry oxidation and the oxide growth rate of $Si_{1-x}Ge_x$ epitaxial layer. Oxidation were performed at 700, 800, 900, and $1,000\;^{\circ}C$. After the oxidation, the results of RBS (Rutherford Back Scattering) & AES(Auger Electron Spectroscopy) showed that Ge was completely rejected out of the oxide and pile up at $Si_{1-x}Ge_x$ interface. It is shown that the presence of Ge at the $Si_{1-x}Ge_x$ interface changes the dry oxidation rate. The dry oxidation rate was equal to that of pure Si regardless of Ge mole fraction at 700 and 800$^{\circ}C$, while it was decreased at both 900 and $1,000^{\circ}C$ as the Ge mole fraction was increased. The dry of idation rates were reduced for heavy Ge concentration, and large oxiidation time. In the parabolic growth region of $Si_{1-x}Ge_x$ oxidation, the parabolic rate constant are decreased due to the presence of Ge-rich layer. After the longer oxidation at the $1,000^{\circ}C$, AES showed that Ge peak distribution at the $Si_{1-x}Ge_x$ interface reduced by interdiffusion of silicon and germanium.

• Tribology and Lubricants
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• 제16권1호
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• pp.22-26
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• 2000

In this paper, the fuction of Zinc-dialkyldithiophosphate (ZnDTP) as an oxidation ingibitor of mineral oils was investigated and compared with 2,6-Di-tert-Butyl-4-Methylphenol (DBMP). Oxidation tests were conducted using an oxygen absorption apparatus. ZnDTP showedanti-oxidation property, and length of induction period prolonged by increasing ZnDTP concentration. The anti-oxidation property of ZnDTP was simmilar to that with DBMP. The amount of hydroperoxide decomposition ability with ZnDTP was much greater than that with DBMP, But the rate constant of radical scavenging with ZnDTP was less than that with DBMP. The anti-oxidation property of ZnDTP seems to by both synergy effect of hydroperoxide decomposition ability and radical scavenging ability.