• Journal of the Korean Chemical Society
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• v.34 no.5
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• pp.445-451
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• 1990

The catalytic ammoxidation of methylpyrazine into cyanopyrazine over a supported vanadium oxides catalyst on ${\gamma}$-alumina was studied in a continuous-flow fixed bed reactor. Various crystalline phases of vanadium oxides were obtained depending on reduction temperatures. And also the activities for the reaction of methylpyrazine into cyanopyrazine were affected by their major oxidation states of the corresponding crystalline phases. The 10${\%}$ vanadium oxides loaded ${\gamma}$-alumina catalyst, which was reduced at 600$^{\circ}C$ under the hydrogen flow for 2 hours, showed the highest activity and the highest selectivity on cyanopyrazine in the ammoxidation of methylpyrazine.Its major crystalline phase was V$_2$O$_3$ with the presence of V$_6$O$_{13}$ and V$_2$O$_4$(VO$_2$) together. And this coexistance seemed to enhance the activity.

• Resources Recycling
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• v.7 no.1
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• pp.34-40
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• 1998

This shdy was invcsligated on reduction rate of EAF dust wth solid carbon cantents. The rate equation for reduction ofEAF dust was obtaincd in the tempcrahlrc range cot 910-108O"C, and the ratio of zinc removal and metallization raho of ironoxides to thc reaction time was also analysed. From the XRD analysis for slag residues '||'&'||'er reaction, the cxistcncc DI themixture of Akemmite[Ca2MgSi2O.] and SiO, was identified.ed.

• Journal of Korean Society of Environmental Engineers
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• v.27 no.5
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• pp.476-485
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• 2005

In this study, abiotic transformation of TNT reduction products via oxidative-coupling reaction was investigated using Mn oxide. In batch experiments, all the reduction products tested were completely transformed by birnessite, one of natural Mn oxides present in soil. Oxidative-coupling was the major transformation pathway, as confirmed by mass spectrometric analysis. Using observed pseudo-first-order rate constants with respect to birnessite loadings, surface area-normalized specific rate constants, $k_{surf}$, were determined. As expected, $k_{surf}$ of diaminonitrotoluenes (DATs) ($1.49{\sim}1.91\;L/m^2{\cdot}day$) are greater about 2 orders than that of dinitroaminotoluenes (DNTs) ($1.15{\times}10^{-2}{\sim}2.09{\times}10^{-2}\;L/m^2{\cdot}day$) due to the increased number of amine group. In addition, by comparing the value of $k_{surf}$ between DNTs or DATs, amino group on ortho position is likely to be more preferred for the oxidation by birnessite. Although cross-coupling of TNT in the presence of various mediator compounds was found not to be feasible, transformation of TNT by reduction using $Fe^0$ followed by oxidative coupling using Mn oxide was efficient, as evaluated by UV-visible spectrometry.

• Proceedings of the KAIS Fall Conference
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• 2007.05a
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• pp.261-263
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• 2007

본 연구는 광전자 촉매시스템을 이용해 $TiO_{2}$ 졸이 코팅된 구형 비드의 광분해 효율에 대해 고찰한 것이다. $TiO_{2}$ 졸이 코팅된 구형 비드인 알루미늄비드, 유리비드, 실리카비드 화이트젤 ($1{\cdot}2{\cdot}3$형) 다섯 가지 비드를 사용하였고 실험은 산화환원지시 약인 메틸렌블루 수용액이 광촉매의 산화환원반웅을 통해 색상 및 홉광도 변화를 통해 환원 청도를 고찰할 목적으로 실행되었다. 소재별 실험 결과, 실험에 사용한 소재 중 실리카비드 화이트첼($1{\cdot}2{\cdot}3$형)만이 반응성을 나타냈다. 이들 $1{\cdot}2{\cdot}3$형은 $TiO_{2}$의 함량을 달리한 비드들이며 1형이 가장 적은 함량을 가지며 3형이 가장 많은 함량을 가지고 있다. 실험 결과 3형이 반응성이 가장 좋은 것을 알 수 있으며, 이 실험에서는 코팅물의 함량과 고정물의 상태가 광촉매 반응에 영향을 주는 것을 알 수 있다.

• Proceedings of the Korean Fiber Society Conference
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• 2001.10a
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• pp.379-381
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• 2001

굴절율 측정에 의하여 당 성분을 정량하는 방법을 이용한 장치로, 글루코오스의 환원성에 기초하여 산화ㆍ환원 반응을 이용한 적정법이나 흡광도 측정법과 비교하여 시약이 필요없고 시간이 단축되는 장점이 있다. 그리고, 보통의 굴절율 측정기(예로 Abbe refractometer)가 당 농도 0.5％일 때의 굴절율 값 단위로 측정되는 한계를 극복하여 본 당 모니터링 장치는 바탕 물질과의 굴절율 차이를 증폭한 값으로 data(differential refractive index)를 얻을수 있으므로 글루코오스 농도 0.01% 단위까지 정량할 수 있어서 0.1% 이하의 저농도도 측정 가능하며 그 이상의 농도 범위에서도 측정 오차를 줄일수 있는 장점이 있다. (중략)

• Korean Journal of Fisheries and Aquatic Sciences
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• v.14 no.2
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• pp.103-115
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• 1981

The cathodic reactions of lead anodic films formed in phosphoric acid, oxalic acid and sodium hydroxide solutions and the reactivities of Di-iso-butylnitrosoamine (DBNA) in sea water at $15\sim30^{\circ}C$ were studied by means of constant current-potential method. Besides, various contants and thermodynamic quantities obtained in the experiment were also do-scribed to explain the reactivities of protons that entered in the anodic film by being transferred across the metal-oxide interface. The electrode reactions of lead anodic film formed in sodium hydroxide solution in 60mM DBNA+0.5M NaCl did not occur because of complete insulator formed on anodic film. The values of $(\partial\triangle E_{H^+}/\partial T)_{i=const}$, estimated with Bead anodic films formed in phosphoric acid in 60mM DBNA+0.5M NaCl and 60mM $DBNA+6\%_{\circ}$ sea water were $-0.006\;V/^{\circ}C\;and\;-0.005\;V/^{\circ}C$, thus being nearly coincided, but the values of $(\partial E_o/\partial T)_{i=o}$ were $0.002\;V/^{\circ}C\;and\;-0.002\;V/^{\circ}C$, being completely inversed.

• Korean Chemical Engineering Research
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• v.45 no.5
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• pp.506-514
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• 2007

To select the best oxygen carrier particle for syngas fueled chemical-looping combustor, the reduction reactivity and carbon deposition characteristics were determined in a thermogravimetric analyzer. Four kinds of oxygen carrier particles (NiO/bentonite, $NiO/LaAl_{11}O_{18}$, $Co_xO_y/CoAl_2O_4$, $NiO/NiAl_2O_4$) were tested with the simulated syngas (30% $H_2$, 10% $CO_2$, 60% CO) as a reduction gas. With each of these particles, the maximum conversion and oxygen transfer capacity increase with increasing the reduction temperature At the given experimental range, the optimum operating temperature to maximize oxygen transfer rate is found to be $900^{\circ}C$ and carbon deposition on the particles could avoid at the temperature above $800^{\circ}C$. Among four kinds of oxygen carrier particles, the NiO-based particles exhibits better reactivity than the CoO-based particle. Moreover, the NiO/bentonite particle produces the best reactivity based on the oxygen transfer rate and the degree of carbon deposition. The measured oxygen transfer rate increases as the metal oxide content in NiO/bentonite particle is increased thereby higher metal oxide contents could provide stable operation of chemical-looping combustor.

• Economic and Environmental Geology
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• v.42 no.5
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• pp.487-494
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• 2009

The purpose of this study was to investigate the feasibility of As(V) reduction by aqueous Fe(II), and subsequent As(III) immobilization by the precipitation of As(III) incorporated magnetite-like material [i.e., co-precipitation of As(III) with Fe(II) and Fe(III)]. Experimental results showed that homogeneous As(V) reduction did not occur by dissolved Fe(II) at various pH values although the thermodynamic calculation was in favor of the redox reaction between As(V) and Fe(II) under the given chemical conditions. Similarly, no heterogeneous reduction of sorbed As(V) by sorbed Fe(II) was observed using synthetic iron (oxy)hydroxide (Goethite, ${\alpha}$-FeOOH) at pH 7. Experimental results for the effect of As(V) on the oxidation of Fe(II) by dissolved oxygen showed that As(V) inhibited the oxidation of Fe(II). These results indicate that As(V) could be stable in the presence of Fe(II) under the anoxic or subsurface environments.

• Journal of the Korean Chemical Society
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• v.11 no.4
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• pp.159-164
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• 1967

An exact expression of the titration fraction as a function of the potential is derived for the cases where the coefficients of the both half reactions involved in the titration are homogeneous. It shows that the potential is independent of the concentration of the reagents not only at the equivalence point but also at all titration fractions. The sharpness of the end point detection by potentiometric method is shown to depend not only on the difference of the normal potentials involved but also strongly on the number of electrons transferred in each half reaction. The inflexion point of the potentiometric titration curve is shown to be slightly off from the equivalence point, including the cases where the number of electrons involved are equal. Completeness of the reaction in the course of titration is analyzed, too, mostly in terms of equilibrium constant, thus most of the results are applicable to any type of equilibrium in a single phase with particular relationship of coefficients of chemical equation.

• Journal of the Mineralogical Society of Korea
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• v.22 no.2
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• pp.107-114
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• 2009

In present study, an alternative process for manufacturing ultra marine blue by using kaolin, sulfur, sodium carbonate, silica, and rosin was investigated. From the experiments, it was found in the reductive calcination process that the temperature variation with the bed height of input materials is relatively high due to the inadequate thermal conductivity of them. It was also found that the color of the ultramarine blue manufactured is sensitive for the shape of the input materials and the calcinations conditions, and specially the heating rate is very important to form ultramarine. For manufacturing green ultramarine by using sulfur, sodium carbonate, silicon, and pine resin, an optimum condition was investigated to be the heating rate region below $0.6^{\circ}C/min$, the reaction temperature of $850^{\circ}C$ and the reaction time of 4 hr. At the oxidative calcination process to manufacture ultra marine blue from green ultramarine, the optimum flow rate of air is $500{\sim}550\;{\ell}/kg$ (green ultramarine) and the reaction temperature is $500{\sim}550^{\circ}C$.