• 한국응용과학기술학회지
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• 제22권4호
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• pp.349-354
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• 2005

It is interesting to discover the reaction kinetics of the newly developed molybdenum containing catalysts. The dissociation/adsorption of nitrogen on molybdenum surface is known to be structure sensitive, which is similar to that of nitrogen on iron surface. The rates over molybdenum nitride catalysts are increased with the increase of total pressure. This tendency is the same as that for iron catalyst, but is quite different from that for ruthenium catalyst. The activation energies of the molybdenum nitride catalysts are almost on the same level, although the activity is changed by the addition of the second component. The reaction rate is expressed as a function of the concentration of reactants and products. The surface nature of $CO_3Mo_3N$ is drastically changed by the addition of alkali, changing the main adsorbed species from $NH_2$ to NH on the surface. The strength of $NH_x$ adsorption is found to be changed by alkali dopping.

• 한국염색가공학회지
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• 제19권4호
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• pp.18-25
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• 2007

Kinetics and mechanism for alkaline hydrolysis of C. I. Disperse Green 9(G-9) of dinitrothiophene disperse dye were investigated. As soon as G-9 contacted with alkali, instant and continuous decreases of color strength of G-9 followed with increasing time. The hydrolysis rate of G-9 increased with increasing alkali, and it was found that alkali appeared first order dependence. The observed rate constants obtained from hydrolysis of various amount of dye were similar values, and calculation of initial rates showed that G-9 hydrolyzed by first order reaction for dye. Therefore it was confirmed that the overall reaction was second order, $SN_2$ of nucleophilic substitution reaction. Increasing temperature enhanced the hydrolysis of G-9. From the results of hydrolysis performed at various temperatures, it was obtained that activation energy(Ea) was 12.6 kcal/mole, enthalpy of reaction(${\triangle}H$) was 12.0 kcal/mole, and entropy of reaction(${\triangle}S$) was $29.8J/mol{\cdot}K$.

• 공업화학
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• 제17권1호
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• pp.33-36
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• 2006

광경화 접착제로 많이 사용되는 우레탄-아크릴레이트 올리고머의 광경화 거동을 자체촉매화 반응모델식을 통해 중합온도 및 올리고머의 관능성에 따른 영향을 확인하여 보았다. 중합온도가 증가함에 따라 최대중합속도는 감소하여 중합온도가 경화 거동에 대한 영향인자임을 확인할 수 있었으며, 반응속도상수 k는 온도증가에 따라 거의 일정한 값을 보이나 반응차수 m과 n은 증가하는 경향을 보였는데 이는 가교구조에 의한 반응성 기의 확산제한 및 유동성의 제한으로 인한 것으로 판단되어진다. 온도증가에 따른 중합속도의 감소는 주로 반응차수 n의 증가에 의해 진행되었다.

• 한국식품과학회지
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• 제19권6호
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• pp.515-519
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• 1987

가열에 의한 생배추 및 절임배추 조직의 동적변화를 Instron을 사용하여 puncture test로 측정연구하였다. $80^{\circ}C$ 범위의 저온에서 데치기와 살균하는 저온장시간 열처리 조작으로 배추 조직을 최대한 유지할 수 있을 것으로 생각되었다. 배추조직의 열에 의한 연화속도는 1차식으로 표현될수 있었다. 데치기 조작에서 $80^{\circ}C$ 이하에서 데치기한 경우 생배추 및 절임배추의 활성화 에너지는 각각 1.4 및 2.8kcal/mol, $80^{\circ}C$이상에서는 각각 31.5 및 42.4kcal/mol로서, $80^{\circ}C$ 이하에서는 배추조직의 연화속도가 온도의 영향을 크게 받지 않았다. 한편 예비열처리 조작인 데치기는 저온살균공정에서 배추조직의 연화에 큰 영향을 미쳐 $80^{\circ}C$이상에서 데치기한 배추는 다음 저온살균공정에서 열처리 온도에 민감하게 영향을 받았다.

• 한국수소및신에너지학회논문집
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• 제18권1호
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• pp.40-45
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• 2007

Methylene blue(MB) was photocatalytically degraded with one-body photoanode and solar simulator to investigate the possible application to both environmental purification and photoelectrochemical cell for hydrogen production. Photoactive titanium dioxide was formed on both sides of Ti plate following steps such as rinsing-annealing-calcination or anodizing(20 V, 30 V)-annealing($350^{\circ}C$, $450^{\circ}C)$ after etching. The prepared titania plate($2cm{\times}2\;cm$, ca 1.6 mg $TiO_2$ on the basis of $1\;{\mu}m$ thickness) was used to degrade MB(10 ppm in 200 mL solution). The reaction tended to follow the Langmuir-Hinshelwood kinetics with zero order. Comparative experiments with Degussa P25 showed the same zero order kinetics when 2 mg of P25 had been used, while the first order kinetics when 200 mg used. This concludes the feasibility of the prepared titania plate as a material for the purification of low-level harmful organics and an electrode or a membrane for photoelectrochemical system for hydrogen production.

• Korean Chemical Engineering Research
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• 제48권6호
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• pp.712-716
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• 2010

염석결정화란 제 3의 성분을 가하여 혼합용매로 만들어 용질의 용해도를 저하시키는 방법으로 염료 용액으로부터 염료 결정화에 염석결정화를 이용하였다. 이번 연구에서 반응성 염료(Reactive Red 218)의 용해도와 결정화 속도를 연구하였다. 그 결과 염료 용액의 용해도는 KCl 농도가 높을수록 용해도가 낮아지는 것을 확인할 수 있었다. 또한 연속식 결정화기에서 반응성 염료(Reactive Red 218)에 대한 결정화 속도식은 결정 성장 속도 $G=6.864{\times}10^{-5}{\Delta}C^{1.207}$와 핵 생성속도 $B^0=4.8{\times}10^{22}{\Delta}C[1.1{\times}10^{-13}+{({\Delta}C)}^{0.7}{M_T}^2]$의 실험식으로 표현할 수 있다.

• Korean Chemical Engineering Research
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• 제58권1호
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• pp.127-134
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• 2020

상용흡착제 실로퓨트에 의한 Taxus chinensis 유래 주요 타르 성분인 아세나프텐의 흡착 특성을 조사하였다. 초기 아세나프텐 농도, 흡착 온도 및 시간에 따른 흡착 데이터를 Langmuir, Freundlich, Temkin 및 Dubinin-Radushkevich 등온흡착식에 적용한 결과, Langmuir 등온흡착식이 가장 적합하였다. 동역학적 흡착 데이터는 유사 이차 속도식에 가장 잘 따름을 알 수 있었다. 열역학적 파라미터로부터 흡착 공정이 적합하며 비자발적 발열이었다. 등량흡착열은 흡착량에 의존하지 않아 실로퓨트의 표면에너지가 균일함을 알 수 있었다.

• 한국세라믹학회지
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• 제38권10호
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• pp.881-885
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• 2001

Kinetics and mechanisms of intermediate phases formation in $Ba(Mg_{1/3}Ta_{2/3})O_3$, obtained by a solid state reaction were studied. $Ba{Ta_2}{O_6}$ and ${Ba_4}{Ta_2}{O_9}$ as intermediate products were first formed at $700^{\circ}C$. $Ba(Mg_{1/3}Ta_{2/3})O_3$ was appeared at $800^{\circ}C$. Several reactions take place on heating process. $Ba{Ta_2}{O_6}$ is found at the first stage of the reaction, and then $Ba{Ta_2}{O_6}$ or ${Ba_4}{Ta_2}{O_9}$ react with MgO to form $Ba(Mg_{1/3}Ta_{2/3})O_3$. The reaction of $Ba(Mg_{1/3}Ta_{2/3})O_3$ formation does not complete until fired at $1350^{\circ}C$ for 60 min. The kinetics of solid-state reaction between powdered reactants was controlled by diffusion mechanism, and can be explained by the Jander's model for three-dimensional diffusion.

• Elastomers and Composites
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• 제50권2호
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• pp.92-97
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• 2015

A study on reaction kinetics for a PTMG/TDI prepolymer with 2,2'-dichloro-4,4'-methylenedianiline (MOCA), of which formulations may be generally used for fabricating high performance polyurethane elastomers, was peformed using non-isothermal differential scanning calorimetry (DSC). A number of thermograms were obtained at several constant heating rates, and analysed using Flynn-Wall-Ozawa (FWO) isoconversional method for activation energy, $E_a$ and extended-Avrami equation for reaction order, n. Urea formation reaction of the present system was observed to occur through the simple exothermic reaction process in the temperature range of $100{\sim}130^{\circ}C$ for the heating rate of $3{\sim}7^{\circ}C/min$. and could be well-fitted with generalized sigmoid function. Though activation energy was nearly constant as $53.0{\pm}0.5kJ/mol$, it tended to increase a little at initial stage, but it decreases at later stage by the transformation into diffusion-controlled reaction due to the increased viscosity. Reaction order was evaluated as about 2.8, which was somewhat higher than the generally well-known $2^{nd}$ order values for the various urea reactions. Both the reaction order and reaction rate explicitly increased with temperature, which was considered as the indication of occurring the side reactions such as allophanate or biuret formation.

• Bulletin of the Korean Chemical Society
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• 제30권10호
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• pp.2259-2264
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• 2009

A new high-energy organic potassium salt, 2-(dinitromethylene)-1,3-diazepentane potassium salt K(DNDZ), was synthesized by reacting of 2-(dinitromethylene)-1,3-diazepentane (DNDZ) and potassium hydroxide. The thermal behavior and non-isothermal decomposition kinetics of K(DNDZ) were studied with DSC, TG/DTG methods. The kinetic equation is $\frac{d{\alpha}}{dT}$ = $\frac{10^{13.92}}{\beta}$3(1 - $\alpha$[-ln(1 - $\alpha$)]$^{\frac{2}{3}}$ exp(-1.52 ${\times}\;10^5$ / RT). The critical temperature of thermal explosion of K(DNDZ) is $208.63\;{^{\circ}C}$. The specific heat capacity of K(DNDZ) was determined with a micro-DSC method, and the molar heat capacity is 224.63 J $mol^{-1}\;K^{-1}$ at 298.15 K. Adiabatic time-to-explosion of K(DNDZ) obtained is 157.96 s.