• Journal of Biosystems Engineering
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• 제23권4호
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• pp.335-342
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• 1998

The objectives of this study were to evaluate respiration characteristics and develop empirical respiratory rate equations for short gain rough rice. The carbon dioxide concentrations generated from mush rice at four level temperatures(10, 20, 30, 4$0^{\circ}C$) and 4 level moisture contents(17.2, 21.5, 25.9, 31.6％, d.b.) were measured by gas chromatography. The respiratory rates' increased exponentially with gain temperature and also with moisture content The relationship between respiratory rate and gain temperature fitted the Arrehenius' and Core's equations very well. Two empirical respiratory rate equations were presented as a function of gain temperature and moisture content. The values of determination coefficient for the developed respiratory rate equations were 0.999, and the result of t-test showed that there were no significant differences between predicted and measured respiratory rates on significance level of 1%. Therefore, it appeared that respiratory rates predicted by the respiratory rate equations agreed well with measured values. An equation for predicting dry matter losses of rough rice during storage was presented by modifying the respiratory rate equations based on chemical reaction of decomposition of carbohydrate.

• 한국산학기술학회논문지
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• 제11권5호
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• pp.1735-1740
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• 2010

추진제 KM10은 NC(Nitrocellulose)를 주원료로 제조된 단기추진제로서 장기저장시 자연분해현상을 일으키는 것으로 알려져 있다. 저장수명추정은 잔류안정제 함량분석을 위해 일반적으로 이용되는 고온가속노화시험을 사용하였으며, 반응속도상수 산출을 위해 Arrhenius 식과 Berthelot 식을 사용하였다. 본 연구 결과에 따르면 Arrhenius 식과 Berthelot 식을 이용하여 추정한 추진제 KM10의 저장수명은 43.72년, 16.53년으로 큰 차이를 보였으며, E. R. Bixon의 연구결과[1]와 비교할 때 Arrhenius Equation을 이용하여 추정한 43.72년이 타당한 것으로 판단된다.

• 한국응용과학기술학회지
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• 제6권2호
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• pp.59-65
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• 1989

The rate constants of the hydrolysis of cinnamanilide derivatives were determined UV spectrometry in $H_2SO_4\;(5{\sim}20N)$, NaOH($5{\sim}11N)\;at\;50{\sim}110^{\circ}C$ and rate equation could be applied over a strong acid and strong base were obtained. Final product of the hydrolysis was a cinnamic acid. The ${\rho}$ values obtained from the slope of linear plots of log $k_{abs}$ vs. Hammet $t{\sigma}$ constants were slightly negatives, Substituents on cinnamanilide showed a relatively small effect, with hydrolysis facilitated be electron donating group. Activation energy(Ea)was also calculated for the hydrolysis of the cinnamanilide. From this reaction rate equation, substituent effect and experimental of rate constants, that the hydrolysis of cinnamanillde was Initiated by the netural molecule of $H_2O$ which do not dissociate at strong acid, and proceeded by hydroxide ion at strong base.

• 대한화학회지
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• 제26권6호
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• pp.407-413
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• 1982

3,4-methylenedioxyphenylmethylene malononitrile에 대한 cysteine의 친핵성 첨가반응 속도를 측정하여 염기성 및 산성용액에서의 반응메카니즘을 제안하였고 넓은 pH범위에서 잘 맞는 반응속도식을 구했다. 이 반응속도식으로 부터, pH 9.0 이상에서는 hydroxide ion 농도에만 비례하고, pH 6.0 이하에서는 cysteine의 중성분자만이 첨가하며, pH 7~9.0에서는 cysteine 중성분자와 그의 음이온이 경쟁적으로 첨가됨을 알 수 있었고 첨가되는 cysteine 중성분자와 음이온의 비도 계산할 수 있었다.

• 한국식품과학회지
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• 제12권2호
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• pp.122-125
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• 1980

표준 도정한 쌀 보리(품종 세도하다까) 및 겉 보리 (수원 18호)의 취반에 대한 기작을 연구하였다. 취반 (취반 온도 $90^{\circ}{\sim}120^{\circ}C$) 후 입자의 경도는 texturometer로 측정하였다. 쌀 보리나 겉 보리는 비슷한 취반양상을 보이며 고온($110^{\circ}C$이상)에서는 갈변 현상과 동시에 입자 자체는 붕괴하면서도 연화도는 계속 증가하였다. 취반 속도는 1차 반응의 식으로 표시될 수 있었으며 취반의 활성화 에너지는 $100^{\circ}C$ 이하에서는 약 16,000cal/mole, $100^{\circ}C$ 이상에서는 약 9,500 cal/mole이었다. 보리의 취반 과정은 다음의 두 기작으로 설명할 수 있었다. 즉 취반 온도 $100^{\circ}C$ 이하에서는 보리의 성분 및 물에 의한 화학 반응이, 취반 온도 $100^{\circ}C$이하에서는 보리의 성분 및 물에 의한 화학 반응이, 취반 온도 $100^{\circ}C$ 이상에서는 취반된 부분으로부터 취반되지 않은 부분 (즉 반응이 진행되고 있는 부분)으로의 물의 확산 속도가 취반 속도를 제한하였다.

• Environmental Engineering Research
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• 제12권1호
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• pp.30-35
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• 2007

Fenton system using homogeneous iron catalyst is very powerful in the degradation of organic compounds, but has a disadvantage to remove Fe ions from water after wastewater treatment. Thus, iron catalyst was bounded to support such as inorganic and polymer materials. The PVP supporting iron catalyst showed a good catalytic performance in degradation of phenol contained in waste water and iron catalyst supported on ${SO_4}^{2-}$ type PVP (KEX 511) showed the best catalytic performance. Also, reaction kinetic study was carried out in this system. Reaction constants on various catalysts was obtained from the pseudo first order equation. Reaction rate constants with the heterogenized $FeCl_2/PVP$ catalyst is a three-fold smaller than that of $FeCl_2$ catalyst.

• 환경위생공학
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• 제19권1호
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• pp.1-7
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• 2004

This study was conducted to supply basic informations on development of water treatment process for the ozonation of ammonia depend on pH variation with or without bromide catalysis. The results were as follows: The oxidation rate of ammonia increased depend on pH increase at ozone/bromide process. It was found that overall kinetics was zero order with respect to reaction time and reaction velocity constant of zero order increased depend on pH increase from 4.9 to 9.5 and the equation of linearization was $k_{o}$ = 0.00565 ${\times}$ [pH] + 0.0069 at ozone/bromide process. The denitrification reaction of ammonia was superior as the pH increase in the presence of bromide.

• 한국세라믹학회지
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• 제18권1호
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• pp.35-40
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• 1981

The kinetics of the dehydration of Ha-dong kaolin was studied isothermally at various temperatures. Dehydration rate was measured by thermogravimetry method in the temperature range of 440~50$0^{\circ}C$ and the particle size range of 170~325mesh. The general equation f($\alpha$)=kt, where $\alpha$ is the fraction reacted in the time and the function f($\alpha$) depends on the reaction mechanism, was applied to this reaction. The function, f($\alpha$) was obtained by application of reduced-time plot and plot of lnln (1-$\alpha$) vs. ln (time), and expressed as (1-$\alpha$) ln (1-$\alpha$)+$\alpha$=kt. The dehydration followed the diffusion-controlled reaction model and gave activation energy of 30Kcal/mole.

• Bulletin of the Korean Chemical Society
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• 제12권6호
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• pp.652-658
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• 1991

The effect of intermolecular collisions in the infrared multiphoton dissociation (IRMPD) of difluorochloromethane was investigated using He, Ar, and $N_2$ as buffer gases. The reaction probability for IRMPD of difluorochloromethane was measured as a function of laser fluence and the buffer gas pressure under unfocused beam geometry. It was observed that the reaction probability was initially enhanced with the increase of buffer gas pressure up to about 20 torr, but showed a decline at higher pressures. The reaction probability increases monotonically with the laser fluence, but the rate of increase diminishes at higher fluences. An attempt was made to simulate the experimental results by the method of energy grained master equation (EGME). From the parameters that fit the experimental data, the average energy loss per collision, $<{\Delta}E>_d$, was estimated for the He, Ar, and $N_2$ buffer gases.

• 한국복합재료학회:학술대회논문집
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• 한국복합재료학회 2004년도 춘계학술발표대회 논문집
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• pp.214-217
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• 2004

The cure kinetics of blends of epoxy(tetraglycidyl-4,4'-diaminodiphenylmethane ; TGDDM)/curing agent(diaminodiphenyl sulfone ; DDS) resin with amine terminated polyetherimide-CTBN-amine terminated polyetherimide triblock copolymer(ABA) were studied using differential scanning calorimetry under isothermal conditions to determine the reaction parameters such as activation energy and reaction constants. By increasing the amount of ABA in the blends, the final cure conversion was decreased. Lower values of the final cure conversions in the epoxy/ABA blends indicated that ABA hinders the cure reaction between the epoxy and curing agents. 1be value of the reaction order, m, for the initial autocatlytic reaction was not affected by blending ABA with epoxy resin, and the value was approximately 1.0. The value of n for the nth order component in the autocatalytic analysis was increased by increasing the amount of ABA in the blends, and the value increased from 2.0-3.4. A diffusion controlled reaction was observed as the cure conversion increased and the rate equation was successfully analyzed by incorporating the diffusion control term for the epoxy/DDS/ABA blends.