• Proceedings of the KOSOMBE Conference
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• v.1998 no.11
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• pp.237-238
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• 1998

The kinetics of sulfite oxidation must be fast and the concentration of sulfite must be low to emulate oxygen uptake by blood. The kinetics were studied yielding a first order rate constant in sulfile, zero order in oxygen. Limitations of the technique were evaluated using the experimental rate constant and an adaptation of Lightfoot's approximation, while the reaction of hemoglobin is reversible and essentially instantaneous, that for sulfite is irreversible and finite. Thus if the approach to saturations not monotonic or if the mass transfer resistance is significantly lowered, e. g. when blood film thicknesses are thinner than a few hundred microns, deviations may occur.

• The Proceedings of the Korean Institute of Illuminating and Electrical Installation Engineers
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• v.11 no.1
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• pp.99-105
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• 1997

In the paper, aging of insulating oil in pole transformer has been studied by performing accelerated thermal aging test. Dissolved gases were extracted by air bubbling method. Concentration of dissolved gases were modified by extraction ratio of each gases in insulating oil. Aging of insulating materials were proceeded by thermal degradation and oxidation reaction. Both of the reactions followed zeroch order kinetics. Formation rate equations for hydrocarbons, carbon oxides, and hydrogen were derived. It was conformed by gas analysis and UV-Visible spectrophotometric method that iron core and copper coil in pole transformer act as catalyst during the aging process.

• Molecules and Cells
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• v.39 no.1
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• pp.26-30
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• 2016

Peroxiredoxins are ubiquitous thiol proteins that catalyse the breakdown of peroxides and regulate redox activity in the cell. Kinetic analysis of their reactions is required in order to identify substrate preferences, to understand how molecular structure affects activity and to establish their physiological functions. Various approaches can be taken, including the measurement of rates of individual steps in the reaction pathway by stopped flow or competitive kinetics, classical enzymatic analysis and measurement of peroxidase activity. Each methodology has its strengths and they can often give complementary information. However, it is important to understand the experimental conditions of the assay so as to interpret correctly what parameter is being measured. This brief review discusses different kinetic approaches and the information that can be obtained from them.

• Journal of Energy Engineering
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• v.15 no.1 s.45
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• pp.8-13
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• 2006

The oxidation behavior of $UO_2$, pellet was studied using an XRD and a thermogravimetric analyzer in the temperature range from 573 to 873 K and in the density range from 94.64 to 99.10% of theoretical density in air. It was found from the XRD study that $UO_2$ was completely converted to $U_3O_8$ in this experimental temperature range. The formation of $U_3O_8$ displays sigmoidal reaction kinetics. The oxidation rate was reduced with density. Induction time for the oxidation of $UO_2$ was delayed with density because of open pore formed in surface of $UO_2$ pellet. The activation energy for oxidation of $UO_2$ was determined to be 89.54 kJ/mol and 34.40 kJ/mol in the temperature range from 573 to 723 K and from 723 to 873 K, respectively.

• Journal of the Korean Ceramic Society
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• v.48 no.1
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• pp.57-62
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• 2011

The T23 steel, whose composition was Fe-2.3%Cr-1.6%W, was arc-melted, and oxidized between $600^{\circ}C$ and $900^{\circ}C$ in air for up to 7 months. The amount of precipitates in the arc-melted microstructure was as large as 11.4 vol.%. The precipitates increased the oxidation rate of the arc-melted T23 steel. Owing to the low amount of Cr in the T23 steel, breakaway oxidation occurred after a few hours during oxidation above $700^{\circ}C$ in both arc-melted and as-received T23 steels. The scales that formed on arc-melted and as-received T23 steels were similar to each other. They consisted primarily of the outer $Fe_2O_3$ layer and the inner ($Fe_2O_3$, $FeCr_2O_4$)-mixed layer. The precipitates increased the microhardness and the oxidation rates.

• Journal of Electrochemical Science and Technology
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• v.12 no.1
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• pp.112-125
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• 2021

The new emerging "High entropy materials" attract the attention of the scientific society because of their simpler structure and spectacular applications in many fields. A novel nanocrystalline high entropy (Be,Mg,Ca,Sr,Zn,Ni)3O4 oxide has been successfully synthesized through mechanochemical treatment followed by sintering and air quenching. The present research work focuses on the possibility of single-phase formation in the aforementioned high entropy oxide despite the great difference in the atomic sizes of reactant alkaline earth and 3d transition metal oxides. Structural properties of (Be,Mg,Ca,Sr,Zn,Ni)3O4 high entropy oxide were explored by confirmation of its single-phase Fd-3m spinel structure by x-ray diffraction (XRD). Further, nanocrystalline nature and morphology were analyzed by scanning electron microscopy (SEM). Among thermal properties, thermogravimetric analysis (TGA) revealed that the (Be,Mg,Ca,Sr,Zn,Ni)3O4 high entropy oxide is thermally stable up to a temperature of 1200℃. Whereas phase evolution in (Be,Mg,Ca,Sr,Zn,Ni)3O4 high entropy oxide before and after sintering was analyzed through differential scanning calorimetry (DSC). Electrochemical studies of (Be,Mg,Ca,Sr,Zn,Ni)3O4 high entropy oxide consists of a comparison of thermodynamic and kinetic parameters of water and hydrazine hydrate oxidation. Values of activation energy for water oxidation (9.31 kJ mol-1) and hydrazine hydrate oxidation (13.93 kJ mol-1) reveal that (Be,Mg,Ca,Sr,Zn,Ni)3O4 high entropy oxide is catalytically more active towards water oxidation as compared to that of hydrazine hydrate oxidation. Electrochemical impedance spectroscopy is also performed to get insight into the kinetics of both types of reactions.

• Journal of Korean Society on Water Environment
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• v.38 no.5
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• pp.211-219
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• 2022

In this study, the effect of liquid height/volume on sonochemical oxidation reactions was investigated in 300 kHz sonoreactors. The gas mixture of Ar/O₂ (50:50) was applied in two modes including saturation and sparging, and zero-order reaction (KI dosimetry) and first-order reaction (Bisphenol A (BPA) degradation) were used to quantitatively analyze sonochemical oxidation reactions. For the zero-order reaction, the highest sonochemical oxidation activity was obtained for the liquid height of 5𝛌, and the lowest height for both the gas saturation and sparging conditions. In addition, the sparging did not enhance the sonochemical oxidation activity for all height conditions except for 50𝛌, where very low activity was obtained. It was found that in sonochemiluminescence (SCL) images the sonochemical active zone was formed adjacent to the liquid surface for the gas sparging condition due to the formation of the standing wave field while the active zone was formed adjacent to the transducer at the bottom due to the blockage of ultrasound. For the first-order reaction, the highest activity was also obtained at 5𝛌 and the comparison based on the reactant mass was not appropriate because the concentration of the reactant (BPA) decreased significantly as the reaction time elapsed. Consequently, it was revealed that the determination of optimal liquid height (ultrasound irradiation distance) based on the wavelength of the applied ultrasound frequency was very important for the optimal design of sonoreactors in terms of reaction efficiency and reactor size.

• Journal of environmental and Sanitary engineering
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• v.19 no.1
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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.

• Electrical & Electronic Materials
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• v.4 no.2
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• pp.97-104
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• 1991

W/Si의 조성비가 2.6인 CVD텅스텐 실리사이드를 어닐링처리 하지 않고 바로 wet oxidation하여 polycide구조에서 다결정 실리콘 내의 인의 농도가 실리사이드의 산화반응 속도에 미치는 영향을 조사하여 직선-포물선적 속도법칙을 토대로 하여 분석 조사하였다. 텅스텐 실리사이드의 산화속도는 다결정 실리콘 내의 도편트 인의 농도가 증가함에 따라 증가하는 것으로 나타났다. 직선적 속도상수와 포물선적 속도상수 모두 인의 농도가 증가함에 따라 증가하는 경향을 보였다. 직선적 속도상수에 대한 활성화 에너지는 인의 농도가 증가함에 따라 감소하였으나 포물선적 속도상수에 대한 활성화 에너지는 인 농도와 무관한 것으로 나타났다.

• Journal of the Korean Chemical Society
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• v.34 no.3
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• pp.297-303
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• 1990

$VO^{2+}-catalyzed oxidation of n-butylamine by hydrogen peroxide shows that the reaction is a first order in the concentration of n-butylamine, acid added, and VO^{2+}$ as catalyst, respectively. The reactions involve the initial formation of an imine intermediate, followed by hydrolysis to butyraldehyde and ammonia. It is suggested that the rate-determining step is a process dehydrogenation of n-butylammine.