• 한국응용과학기술학회지
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• 제12권2호
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• pp.145-150
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• 1995

The Kinetics velocity for hydrolysis reaction of vanillylidene imine derivatives has been measured by ultra-violet ray spectrophotometer in 20wt% $dioxane-H_2O$ at $25^{\circ}C$. It was measured the reaction rate Constant of vanillylidene imine derivatives that can be applied widely following to pH-change at $25^{\circ}C$. Final products that hydrolyzed the vanillylidene imine certified in vanillin and aniline derivative, and the effect of substitution radical that has affected on hydrolysis reaction was largely promoted to reaction rate by electron attrating group in acidity and electron donoring group in basic. From the results of rate constant to hydrolysis reaction, substituent radical effect and final products. It has certified the hydrolysis reaction mechanism of vanillylidene imine derivatives.

• 한국자동차공학회논문집
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• 제9권2호
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• pp.185-191
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• 2001

In many papers, the powertrain system generally has been madeled as one-dimensional torque model. One-dimensional powertrain model may calculate the torque correctly but it does not consider the non-rotational degrees-of-freedom of the powertrain components and the interaction of these degrees-of-freedom with the vehicle body frame and suspension. To consider the non-rotational degrees of freedom, the differential is modeled as a three-dimensional rigid body in this paper. A constant velocity joint is newly formulated and a relative constraint is also formulated to model the motion transfer due to gear ratio of the differential. Implementing the proposed powertrain system in the multibody model, more detail dynamic responses can be obtained. Obtained outputs such as reaction torques on the constant velocity joint and reaction forces on the rack can be useful data in the design of a powertrain.

• 대한환경공학회지
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• 제32권11호
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• pp.1046-1053
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• 2010

본 연구의 목적은 생활폐기물에 저품위 무연탄의 혼합 후 열분해 반응 특성을 연구하는데 목적이 있다. 반응 변수로 혼합율, 반응온도, 승온속도에 따른 열분해조건을 고찰하였다. 그 결과, 저품위 무연탄 20 wt.%를 첨가한 혼합 시료가 3,500 kcal/kg 이상의 저위발열량 확보를 위한 최적의 혼합비로 나타났다. 가장 높은 반응속도상수 도출을 위해서는 $700^{\circ}C$의 조건에서 이루어 질 것으로 판단되었다. 또한 시간당 온도의 비가 증가할수록 반응속도상수가 선형적으로 높게 나타났으나, 열분해 시 전력비 상승 및 열분해 생성 char의 수율 등을 고려하여 더 낮은 승온속도에서 열분해가 이루어져야 할 것으로 판단된다.

• 한국환경과학회지
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• 제6권4호
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• pp.399-407
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• 1997

The pyrolysis reactions of atomic hydrogen with chloroform were studied In a 4 cm 1.6. tubular flow reactor with low flow velocity 1518 cm/sec and a 2.6 cm 1.4. tubular flow reactor with high flow velocity (1227 cm/sec). The hydrogen atom concentration was measured by chemiluminescence titration with nitrogen dioxide, and the chloroform concentrations were determined using a gas chromatography. The chloroform conversion efficiency depended on both the chloroform flow rate and linear flow velocity, but 416 not depend on the flow rate of hydrogen atom. A computer model was employed to estimate a rate constant for the initial reaction of atomic hydrogen with chloroform. The model consisted of a scheme for chloroform-hydrogen atom reaction, Runge-Kutta 4th-order method for Integration of first-order differential equations describing the time dependence of the concentrations of various chemical species, and Rosenbrock method for optimization to match model and experimental results. The scheme for chloroform-hydrogen atom reaction Included 22 elementary reactions. The rate constant estimated using the data obtained from the 2.6 cm 1.4. reactor was to be 8.1 $\times$ $10^{-14}$ $cm^3$/molecule-sec and 3.8 $\times$ $10^{-15}$ cms/molecule-sec, and the deviations of computer model from experimental results were 9% and 12% , for the each reaction time of 0.028 sec and 0.072 sec, respectively.

• 설비공학논문집
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• 제13권7호
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• pp.637-646
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• 2001

VOC(Volatile Organic Compound) removal characteristics in continuous flow reactors have been numerically investigated. The photocatalytic reaction have been simulated with the binding constant and the reaction rate constant obtained from experimental data for the constant-volume batch reactor, and then VOC abatement in continuous flow reactors with the same conditions as those of batch reactor has been analyzed. The standard 4\kappa-\varepsilon$ model and mass conservation equation have been employed for numerical calculation, and heterogeneous reaction rate has been used in terms of the boundary condition of the conservation equation. in the case of the continuous flow reactor, reaction characteristics have been estimated with various inlet velocities and with different number of baffles. The result shows that the concentration distribution and flow patterns are strongly affected by the inlet velocity, and that with the increased inlet velocity, VOC removal rate is increased, while removal efficiency is decreased. This result may be useful in the design of reactors with improved VOC removal efficiency.

• 한국윤활학회:학술대회논문집
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• 한국윤활학회 1998년도 제28회 추계학술대회
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• pp.306-312
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• 1998

This paper describes syntheses of thickener for di-urea grease using constant velocity joint. The thickeners of di-urea grease were synthesized by reaction of diisocyanate with various alkylamines, hexylamine, octylamine, stearylamine and cyclohexylamine at high temperatxire. The synthesized thickener were analyzed by FT-IR spectroscopy and two kinds of Mass spectroscopy (EI & FAB). Dropping point and Consistency of synthesized di-urea grease were determined.

• 산업식품공학
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• 제15권2호
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• pp.155-161
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• 2011

본 실험은 압출성형을 통한 저DE덱스트린 제조공정을 확립하기 위해서 수분함량 25, 35% 배럴온도 100, $120^{\circ}C$, 스크루 회전속도 150, 250 rpm에서 압출성형한 전분을 알 파아밀라아제로 당화시켰을 때 당화특성을 연구하였다. 수 분용해지수는 원료전분 수분함량이 25%로 감소할 경우 증 가되었으며, 수분흡착지수도 수분의 감소와 함께 전체적으 로 증가하였다. 환원당함량의 경우 수분함량이 낮고 배럴온 도 높을수록 증가되었다. 120 분간 당화 후 DE 63.8로 높 게 나타났다. 비기계적 에너지 투입량(SME)의 증가와 함께 수분용해도는 증가하는 경향이었다. 또한 수분함량의 감소 와 함께 비기계적 에너지 투입량과 수분용해도는 증가하였 다. 페이스트점도는 원료전분의 수분이 낮고, 스크루 회전 속도가 증가할수록 전분사슬의 절단에 따라 저온최고점도 가 감소하는 경향을 보였다. 초기반응속도는 수분함량이 25%로 낮고 배럴온도 $120^{\circ}C$, 스크루 회전수 250 rpm에서 $2.26{\times}10^{-3}mmol/mL{\cdot}min$로 가장 높았다. 시중 호화전분 $1.83{\times}10^{-3}mmol/mL{\cdot}min$에 비해서도 높은 결과를 보였다. 당화속도상수는 히구치모델을 응용하였으며, 수분함량이 낮 고 배럴온도가 $120^{\circ}C$일 때 전체적으로 높게 나타났다. 본 실험에서 초기반응속도, 당화속도상수, 당화수율 등을 고려 할 때, 최적조건은 수분함량 25%, 배럴온도 $120^{\circ}C$, 스크루 회전속도 250 rpm이었다.

• 한국윤활학회:학술대회논문집
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• 한국윤활학회 1999년도 제30회 추계학술대회
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• pp.49-56
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• 1999

A material was formulated with Phenol novolac and HEXA only. The cure kinetics and thermal characteristics of phenol novolac with various HEXA contents were peformed by differential scanning calorimetry and thermal gravimetric analysis. All kinetic parameters of the curing reaction including the reaction order, activation energy, and rate constant were calculated and reported. The results indicate that the curing reaction goes through an autocatalytic kinetic mechanism. The friction and wear characteristics of this material were determined using friction material testing machine. The friction coefficient of phenol novolac with various HEXA contents was determined using the PV(pressure & velocity) factor. The most stable and highest friction coefficient with a various pressure and velocity condition was found at HEXA 10 wt.% material. The specific wear rate per unit sliding distance with a various HEXA contents was reported.

• 약학회지
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• 제19권2호
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• pp.101-110
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• 1975

p-Chloronitrobenzene(substrate) and p-nitrophenetole (product) were quantitatively analyzed to know the degree of extent of reaction in the process of time. The calibration curve was prepared by the internal satndard method in gaschromatography. 2,6-Dimethyl-naphthalene was used as internal standard. The rate constant(k), the reaction velocity in various concentrations of NaOH altered, and the formation of byproducts(azo-compound and p-nitrophenol) with the amounts of MnO$_{2}$ and NaOH altered, were studied. From the results of these of MnO$_{2}$ and NaOH altered, were studied. From the results of these experiments, this reaction was second order and the rate constant was k=10.3 $\times$ 10$^{-3}$ mole$^{-21$. When p-chloronitrobenaene 1 pt. NaOH 0.56pts. MnO$_{2}$ 0.5pts. and ethanol 25 pts-were reacted about 10 hours, p-nitrophenetole was nearly quantitatively obtained without byproducts.

• 대한화학회지
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• 제10권4호
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• pp.175-180
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• 1966

Polarography에 의한 反應速度測定法 은 여러가지가 있고 또 많이 硏究되어 왔다. 그러나 그의 應用은 그렇게 많지 않으며, 본 실本 實驗에서는 Delabay의 圖解法과 Koutecky式을 利用하여 몇 가지 ion의 陰極反應速度를 求하고 이들 Data를 써서 簡易速度式을 檢討하였다.