• Journal of the Korean Chemical Society
• /
• v.31 no.3
• /
• pp.280-286
• /
• 1987

The effect of substituent inleaving group on the rates of reactions of phenacyl substituted-benzenesulfonates with pyridine was determined conductometrically in acetonitrile and in methanol at 35, 45, and $55^{\circ}C$, respectively. The reaction rate became faster in proportion to electron-attracting ability of substituent, which indicates that the substituent in leaving group can directly control reaction rate. It was shown that the specific to the carbonyl carbon as the rate-determining step.

• Journal of the Korean Society of Safety
• /
• v.8 no.3
• /
• pp.83-90
• /
• 1993

직류 아아크 용접시 아아크 프라스마와 용융 금속 사이의 계면에서 일어나는 전기 화학 반응이 용착금속 내의 산소와 질소의 함량에 미치는 영향이 고찰되었다. 열 화학 반응 뿐만 아니라 전기 화학 반응도 용접부의 산소 및 질소의 함량을 결정하는 중요한 반응 메카니즘이라는 것과 전기 화학 반응의 양을 결정하는 것은 단위 면적당 통과하는 전류의 양을 조절하는 용접 전류와 용접 속도라는 것이 실험적으로 입증되었다. 따라서 이 연구 결과는 아아크 용접시 적당한 용접 조건의 선택뿐만 아니라 용접 재료의 설계 또는 선택에 중요한 지침을 준다.

• Journal of the Korean Chemical Society
• /
• v.29 no.4
• /
• pp.448-451
• /
• 1985

Pseudo first-order rate constants for reactions of seven m- or p- phenyl-ring substituted 3,5-diphenyl 1,2,4-dithiazolium triodides with hydrazine in excess, in pyridine, were determined by a UV spectrophotometry. For these reactions, calculated some activation parameters, identified the reaction products, and investigated the effect of substituent on the reaction rate. These reactions were accelerated by electron-withdrawing substituents and obeyed the Hammett rule. From the observed kinetics, a reaction mechanism was proposed.

• Applied Chemistry for Engineering
• /
• v.26 no.1
• /
• pp.67-73
• /
• 2015

Using a computational fluid dynamics technique, the flow characteristics and particle residence time in a Taylor reactor were studied. Since flow characteristics in a Taylor reactor are dependent on the operating conditions, effects of the inlet flow velocity and reactor rotational speed were investigated. In addition, the particle residence time of $LiNiMnCoO_2$ (NMC), which is a cathode material in lithium-ion battery, is estimated in the Taylor vortex flow (TVF) region. Without considering the complex chemical reaction at the inlet, the effect of Taylor flow was studied. The results show that the particle residence time increases as the rotating speed increased and the flow rate decreased.

• Journal of the Korean Chemical Society
• /
• v.17 no.6
• /
• pp.411-415
• /
• 1973

The reaction between cyanide ion and triphenyl methane dyes is subject to marked catalysis by cationic micelles of cetyltrimethyl ammonium bromide(CTABr) and retarded by anionic micelles of sodium lauryl sulfate(NaLS). Added salts, anions inhibit the catalysis by CTABr, and cations, especially $Zn^{++},\;Cd^{++}$ decrease the retardation of the reaction rates in the presence of NaLS. The kinetic effects of the ionic micelles are much larger in water than in ethanol-water, methanol-water, propanol-water and acetone-water, but strange solvent effects, acceleration the reaction rates, was found in the reaction with malachite green in water-methanol system.

• Journal of the Korean Chemical Society
• /
• v.35 no.2
• /
• pp.111-118
• /
• 1991

The kinetic of the gas phase reactions of ozone(0.5 torr) with sulfur dioxide was studied. The SO2 reaction was conducted in the 7∼22 torr range at 90∼155$^{\circ}$C. The reaction rate was faster than the reaction rate of O$_3$ in the presence of CO$_2$ alone. The reaction of O$_3$ with SO$_2$ follows the rate law: -d(O$_3)/dt=k_0(SO_2)(M)(O_3)+2k _1(SO_2)(O_3$). The first term of this rate law arises from a third order molecular reaction predominating in the lower temperature range and gave a rate constant k$_0$ = (9.35 $\pm$ 8.6) ${\times}$ 10$^9$e$^{-(11.05{\pm}2.04)kcal/RT}(M^{-2}s^{-1}$). The second term of the above rate law derived from a second order thermal decomposition reaction which was the major part of the reaction and gave a rate constant k$_0 =(9.35{\pm}8.6){\times}10^9e^{-(11.05{\pm}2.04)kcal/RT}(M^{-2}s^{-1}$). The overall reaction proceeds with kinetics of complex order composed mainly of second order and third order components.

• Journal of the Korean Chemical Society
• /
• v.38 no.8
• /
• pp.552-561
• /
• 1994

The cis → trans thermal isomerization of azobenzene derivatives has been studied. A sizable solvent effect on the rates for thermal isomerization of push-pull azobenzenes are observed. It is suggested that the isomerization proceeds via a rotational mechanism. For non push-pull azobenzenes, the lack of solvent effects on the rate of isomerization was observed. This suggests that the isomerization proceeds via an inversional mechanism for non push-pull azobenzenes.

• Journal of the Korean Chemical Society
• /
• v.19 no.2
• /
• pp.123-129
• /
• 1975

The rate constants of the hydrolysis of phenylvinylsulfone were determined by ultraviolet spectrophotometry at various pH and a rate equation which can be applied over wide pH range was obtained. The reaction mechanism of hydrolysis of phenylvinylsulfone and especially the catalytic contribution of hydroxide ion which did not study carefully before in acidic media, can be fully explained by the rate equation obtained. The rate equation reveals that: below pH 7, the reaction is initiated by the addition of water molecule to phenylvinylsulfone. At above pH 9, the overall rate constant is only dependent upon the concentration of hydroxide ion.

• Journal of the Korean Society of Propulsion Engineers
• /
• v.19 no.1
• /
• pp.33-41
• /
• 2015

The kinetic analysis of energetic materials using Differential Scanning Calorimetry (DSC) is proposed. Friedman Isoconversional method is applied to DSC experiment data and AKTS software is used for analysis. The proposed kinetic scheme has considerable advantage over the standard method based on One-Dimenaionl Time to Explosion (ODTX). Reaction rate and product mass fraction simulation are conducted to validate extracted kinetic scheme. Also a slow cook-off simulation is implemented on $B/KNO_3$ for validating the applicability of the extracted kinetics scheme to a practical thermal experiment.

• Applied Chemistry for Engineering
• /
• v.10 no.6
• /
• pp.885-888
• /
• 1999

This study was carried out to determine the reaction kinetic constant of the dehydration - thermal decomposition of $Na_2B_4O_7{\cdot}10H_2O/Na_2B_4O_7{\cdot}5H_2O$ and to investigate the durability during the repeated use of a chemical heat-storage material and the reproducibility of reaction system. The order of the dehydration reaction was 1st-order. The reaction rate was directly proportional to a partial pressure difference of water steam. The kinetic constant was 0.27 and the reproducibility of dehydration reaction for a kinetic constant and a reaction order was excellent. The activity variation in the durability test of a chemical heat-storage material was within range of ${\pm}5%$ during the repeatedly use in several times.