• 대한기계학회논문집B
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• 제20권5호
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• pp.1671-1678
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• 1996

In external chemical vapor deposition processes including VAD and OVD the distribution of flame-synthesized silica particles is determined by heat and mass transfer limitations to particle formation. Combustion gas flow velocities are such that the particle diffusion time scale is longer than that of gas flow convection in the zone of particle formation. The consequence of these effects is that the particles formed tend to remain along straight smooth flow stream lines. Silica particles are formed due to oxidation and hydrolysis. In the hydrolysis, the particles are formed in diffuse bands and particle formation thus requires the diffusion of SiCl$\_$4/ toward CH$\_$4//O$\_$2/ combustion zone to react with H$\_$2/O diffusing away from these same zones on the torch face. The conversion kinetics of hydrolysis is fast compared to diffusion and the rate of conversion is thus diffusion-limited. In the language of combustion, the hydrolysis occurs as a Burke-Schumann process. In selected conditions, reaction zone shape and temperature distributions predicted by the Burke-Schumann analysis are introduced and compared with experimental data available. The calculated centerline temperatures inside the reaction zone agree well with the data, but the calculated values outside the reaction zone are a little higher than the data since the analysis does not consider diffusion in the axial direction and mixing of the combustion products with ambient air. The temperatures along the radial direction agree with the data near the centerline, but gradually diverge from the data as the distance is away from the centerline. This is caused by the convection in the radial direction, which is not considered in the analysis. Spatial distribution of silica particles are affected by convection and diffusion, resulting in a Gaussian form in the radial direction.

• 공업화학
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• 제8권3호
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• pp.502-509
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• 1997

방향족 오염물을 UV산화-고도산화처리기술로 처리할 때, 여러 가지 반응조건에 따른 분해효율에 대해 고찰하였다. 벤젠 50ppm, 에틸벤젠 150ppm, 크실렌 250ppm을 각각 초기농도로하여 UV조사 하에서 시간변화에 따른 분해실험을 행한 결과, 반응 1시간 후 약 95% 이상의 분해율을 나타내었으나, 톨루엔의 경우에는 43%의 분해율을 보였다. 단일성분이 혼합성분에서 보다 분해가 좋았으며, pH변화에서는 벤젠은 pH변화에 관계없이 분해가 잘 되었으며, 에틸벤젠 92%(pH 4.0), 90%(pH 6.4), 91%(pH 10.0), 크실렌 95%(pH 4.0), 90%(pH 6.4), 92%(pH 10.0), 그러나 톨루엔은 80%(pH 4.0), 43%(pH 6.4), 70%(PH 10.0)의 분해율을 나타내었다. 방향족 오염물의 TOC 감소는 에틸벤젠을 제외하고는 유사 1차 반응속도식에 일치하였으며, 이로부터 속도상수를 결정할 수 있었다.

• 대한화학회지
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• 제16권3호
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• pp.157-165
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• 1972

Ammonium metavanadate의 熱分解過程을 spring balance와 示差熱分析에 의하여 調査하였다. 分解는 $180^{\circ}C{\sim}220^{\circ}C$와 $310^{\circ}C{\sim}330^{\circ}C$이 두 溫度範圍에서 일어나며 最終生成物은 $V_2O_5(orange yellow)$임을 알았다. 第一段階分解는 $NH_3$와 $H_2O$가 2:1의 比로 放出되는 過程임을 $NH_3$의 定量, omegatron mass spectrometer에 의하여 알았으며, 第二段階의 分解는 $NH_3,\;H_2$)外에 N2도 放出된다는 것을 gas chromatography, omegatron mass spectrometer에 의하여 認知하였다. 分解生成物을 X-ray 回折에 의하여 分析한 結果는 空氣中에서의 分解生成物은 $V_2O_5$의 組成을 가진 것이 生成되었음을 確認하였다. 또한 $NH_4VO_3$ 熱分解에 있어서의 活性化에너지는 各各 41.4 kcal/mole 64.4 kcal/mole의 값을 갖었음을 알았다.

• 한국지반환경공학회 논문집
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• 제13권9호
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• pp.69-74
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• 2012

본 연구에서는 염기성 수산화이온을 이용한 TNT의 분해 특성을 조사하였다. 이를 위해 TNT 처리 시 분광학적인 변화 특성을 관찰하고, pH 영향 및 반응생성물에 대해 정량적으로 조사하였다. 실험결과, pH=12에서 가수분해에 의해 TNT 수용액이 갈색을 띄는 파장 400-600nm 범위 내에서 흡광도가 증가함을 관찰하였다. 수용액 상의 pH=12에서 TNT 가수분해 시 pseudofirst-order 속도상수는 $0.0022min^{-1}$으로 나타났으며, 그 반응속도는 매우 느린 것으로 초기 TNT 농도인 $44{\mu}M$이 약 90% 정도 분해되려면 약 1,047min(17.44hrs)이 소요될 것으로 예상되었다. 반응 생성물로는 아질산이온과 포름산이 주로 생성되며, 기타 미량 성분으로 질산이온, 옥살산 등이 확인되었다.

• 공업화학
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• 제10권3호
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• pp.467-476
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• 1999

공기에 의한 n-butane의 산화로부터 무수마레인산을 합성하는 고정층 촉매 반응기의 거동을 조사하였다. 대류-확산-반응기구로 묘사되는 고정층 촉매반응기의 거동은 Langmuir-Hinshelwood형의 반응속도식 및 비정상상태 이차원 유사균일상 모델을 적용 조사하였다. 예측모델은 Sharma의 pilot-plant 실험 결과인 단일층 반응기의 축방향 온도 및 수율 분포에 대한 최적적합을 통한 최적매개변수 추정에 의해 구성하였다. 또한 예측모델은 단일층 반응기와 통일한 수율 및 전화율을 생성시킬 수 있도록 모사된 불균열활성의 이중층 반응기가 열점에서 $8.96^{\circ}C$ 낮은 온도 상승을 일으켰다. 단일과 이중층 반응기의 가능한 조업조건 (냉매온도, 반응물의 농도, 온도 및 유량)변화에 대한 매개변수 감응도를 조사한 결과 동일한 조업 조건하에서 이중층 반응기가 단일층 반응기에 비해 더 넓은 조업범위는 물론 전화율 및 수율이 다소 높게 나타났다.

• 한국축산식품학회지
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• 제32권5호
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• pp.598-603
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• 2012

Beef qualities which can be properly predicted by time-temperature integrator (TTI), a chromatic indicator, were selected in terms of its similarity of temperature dependence between beef qualities and TTI, denoted by Arrhenius activation energy ($E_a$). The high similarity is required to afford accurate prediction. A devised enzymatic TTI based on laccase (an oxidase), which catalyses the oxidation on 2,2'-azino-bis-(3-ethylbenzothiazoline-6-sulphonic acid) producing color development, was applied. The factors of beef quality, such as volatile basic nitrogen (VBN), pH, color (CIE $L^*$, $a^*$), Warner-Bratzler shear force (WBSF), Pseudomonas spp. count, and lactic acid bacteria (LAB) count were considered for the selection. $E_a$ (55.48 kJ/mol) of the TTI was found to be similar to those of the beef qualities (all referred) in the order of LAB count (53.54 kJ/mol), CIE $a^*$ value (61.86 kJ/mol), pH (65.51 kJ/mol), Pseudomonas spp. Count (44.54 kJ/mol), VBN (67.98 kJ/mol), WBSF (40.67 kJ/mol), and CIE $L^*$ value (33.72 kJ/mol). The beef qualities with more similar $E_a$ to that of the TTI showed less difference between real and TTI predicted levels. In conclusion, it was found out that when applying TTI to food packages, their $E_a$ similarity should be checked to assure accurate estimation of food quality levels from TTI response.

• 환경생물
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• 제18권3호
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• pp.307-313
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• 2000

석유화학 공업으로부터 생산되는 방향족 탄화수소 화합물질들은 여러 가지 산업과정에서 널리 활용되고 있으나, 자연계에 오염될 때에는 쉽게 분해되지 않는다는 점에서 환경 오염물질로 주목받고 있다. 방향족 탄화수소 물질의 미생물 분해는 산화반응에 의한 benzene고리의 개환으로부터 시작되기 때문에 이 개환 작용을 갖는 미생물의 분리와 함께 그 분해 기능을 연구하는 것은 매우 중요한 일이다. 본 연구에서는 여천 화학공업단지 폐수로부터 benzoate와 catechol 등의 방향족 탄화수소에 대하여 분해능이 우수한 균주를 분리하여 생화학적 특성과 세포 지방산 분석에 의하여 동정한 결과 Pseudomonas putida로 밝혀졌다. 따라서 이 균주를 Pseudomonas putida Z104라 명명한 후, benzoate와 catechol의 분해과정을 검토하였다. Pseudomonus putida Z104의 catechol분해능에 대하여 환경요소의 영향을 실험한 결과, 3$0^{\circ}C$와 pH 7.0 그리고 0.5mM의 농도에서 왕성한 세포의 생장과 catechol의 분해능을 보였으다. 그러므로 Z104 균주는 benzoate를 연속적으로 완전분해시키는 유전자를 모두 가지고 있다는 점에서 활용가치가 있는 균주라고 판단된다.

• Biomolecules & Therapeutics
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• 제20권6호
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• pp.562-568
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• 2012

Cytochrome P450 BM3 (CYP102A1) from Bacillus megaterium is a self-sufficient monooxygenase that consists of a heme domain and FAD/FMN-containing reductase domain (BMR). In this report, the reduction of 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and 5-cyano-2,3-ditolyl tetrazolium chloride (CTC) by BMR was evaluated as a method for monitoring BMR activity. The electron transfer proceeds from NADPH to BMR and then to BMR substrates, MTT and CTC. MTT and CTC are monotetrazolium salts that form formazans upon reduction. The reduction of MTT and CTC followed classical Michaelis-Menten kinetics ($k_{cat}=4120\;min^{-1}$, $K_m=77{\mu}M$ for MTT and $k_{cat}=6580\;min^{-1}$, $K_m=51{\mu}M$ for CTC). Our continuous assay using MTT and CTC allows the simple, rapid measurement of BMR activity. The BMR was able to metabolize mitomycin C and doxorubicin, which are anticancer drug substrates for CPR, producing the same metabolites as those produced by CPR. Moreover, the BMR was able to interact with CYP1A2 and transfer electrons to promote the oxidation reactions of substrates by CYP1A2 and CYP2E1 in humans. The results of this study suggest the possibility of the utilization of BMR as a surrogate for mammalian CPR.

• Journal of Pharmaceutical Investigation
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• 제28권2호
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• pp.121-126
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• 1998

The solubility and physicochemical stability of caroverine hydrochloride (CRV), an antispasmodic, in buffered aqueous solutions were studied using a reverse phase high performance liquid chromatography. The solubilty of the drug at pH 2.76-5.40 was similar at the range 31.9-36.2 mg/ml $(34^{circ}C)$, but, at the pH higher than 6.0, markedly decreased. The use of polyethylene glycol 400 as a cosolvent did not increase the solubility at any compositions examined. Moreover. increasing molar concentration of aqueous phosphate buffer from 0 to 0.5 M remarkably decreased the solubility. The degradation of CRY followed the apparent first-order kinetics. The degradation was accelerated with decreasing pH and increasing storage temperature. The half-lives for the degradation of CRY (1.0 mg/ml) at pH 1.28. 4.01 and 5.93 $(45^{\circ}C)$ were 2.8, 31.4 and 124 hr. respectively. The pHs of incubated solutions were to some extent lowered perhaps due to the formation of acidic degradation products. The addition of disodium edetate (0.01%) to the CRY solution (pH 4.95) retarded 2.5 times the degradation rate at $45^{\circ}C$, but the use of sodium bisulfite (0.1%) accelerated 2.9 times the rate. The activation energy for the CRY solution (20 mg/ml. pH 5.4) containing 0.01% EDTA was calculated to be 5.98 kcal/mole. When the solution was stored under nitrogen displacement in ampoule, there was no significant degradation even after 3 months at $40^{\circ}C$, indicating that protection from oxidation by air (oxygen) is essential for the complete stabilization of CRY solution.

• Environmental Engineering Research
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• 제22권2호
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• pp.203-209
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• 2017

Innovations in the biofiltration process can provide effective solutions to overcome crucial water pollution problems. The elimination of pollutants is a result of the combined effects of biological oxidation, adsorption and filtration processes. This research aims to evaluate the performance of quartz sand biofiltration for removing total suspended solids, turbidity, color, organic matter, and ammonium from polluted river water and develop an empirical model for designing quartz sand biofilters for the treatment of polluted river water. Experiments were conducted using two biofilter units filled with quartz sand as filter media. A set of experiments were performed to evaluate the effect of hydraulic retention time on biofilter performance in removing water contaminants. The kinetics of organic matter removal were also determined to describe the performance of the biofilter. The results show that biofiltration can significantly remove river water pollutants. Removal efficiency depends on the applied hydraulic retention time. At a hydraulic retention time of two hours, removal efficiencies of total organics, ammonium and total suspended solids were up to 78%, 82%, and 91%, respectively. A model for designing quartz sand biofiltration has been developed from the experimental data.