• Environmental Sciences Bulletin of The Korean Environmental Sciences Society
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• v.4 no.2
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• pp.95-102
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• 2000

Methane combustion over perovskite-type oxides prepared using the malic acid method was investigated. To enhance the catalytic activity, the perovskite oxides were modified by the substitution of metal into their A or B site. In addition, the reaction conditions, such as the temperature, space velocity, and partial pressure of the methane were varied to understand their effect on the catalytic performance. With the LaCoO3-type catalyst, the partial substitution of Sr or Ba into site A enhanced the catalytic activity in the methane combustion. With the LaBO3(B=Co, Fe, Mn, Cu)-type catalyst, the catalytic activities were exhibited in the order of Co>Fe Mn>Cu. Futhermore, the partial substitution of Co into site B enhanced the catalytic activity, whereas an excess amount of Co decreased the activity. The surface area and catalytic activity of the perovskite catalysts prepared using the malic acid method showed higher values than those prepared using the solid reaction method. The catalytic activity was enhanced with decreased methane concentration and with a decrease in the space velocity.

• Journal of the Korean Society of Safety
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• v.3 no.1
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• pp.7-13
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• 1988

The oxides in perovskite type, $LaMO_3$ (M=Ni, Cr, Fe, Co), compared with gas sensors which have been used, were synthesised and then examined sensor response comparatively in order to make a thick film gas sensor having a good gas selectivity, durability and simple manufacturing. The oxides in perovskite type, $LaFe_{1-x}O_3$ (x=0.2, 0.4, 0.6, 0.8), which a part of Fe was replaced with Co, were examined with regard to their electric resistance with variable temperature and sensor response for carbon monoxide gas.

• Clean Technology
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• v.18 no.3
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• pp.259-264
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• 2012

Perovskite-type oxides were successfully prepared using malic acid method, characterized by TG/DTA, XRD, XPS, TEM and $H_2$-TPR and their catalytic activities for the combustion of benzene were determined. Almost of catalyst showed perovskite crystalline phase and 15-70 nm particle size. The $LaMnO_3$ catalysts showed the highest activity and the conversion reaches almost 100% at $350^{\circ}C$. The catalysts were modified to enhance the activity through substitution of metal into the A or B site of the perovskite oxides. In the $LaMnO_3$-type catalyst, the partial substitution of Sr into site the A-site enhanced the catalytic activity in the benzene combustion. In addition, the partial substitution of Co or Cu into site the B-site also enhanced the catalytic activity and the catalytic activity was in the order of Co > Cu > Fe in the $LaMn_{1-x}B_xO_3$ (B = Co, Fe, Cu) type catalyst.

• Journal of Korean Society for Atmospheric Environment
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• v.14 no.1
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• pp.25-33
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• 1998

We have studied the reduction of NO by propane over perovskite-type oxides prepared by malic acid method. The catalysts were modified to enhance the activity by substitution by substitution of metal into A or B site of perovskite oxides. In addition, the reaction conditions, such as temperature, $O_2$ concentration, space velocity have been studed. In the $LaCoO_3$ type catalyst, the partial substitution of Ba, Sr into A site enhanced the catalytic activity in the reduction of NO. In the $La_{0.6}Sr_{0.4}Co_{1-x}Fe_xO_3(x=0 \sim 1.9)$ catalyst, the partial substitution of Fe into B site enhanced the conversion of NO, but excess amount of Fe decreased the conversion of NO. The surface area and catalytic activity of perovskite catalysts prepared by malic acid method showed higher values than those of solid reaction method. In the $La_{0.6}Sr_{0.4}Co_{1-x}Fe_xO_3$ catalyst, the conversion of NO increased with increasing $O_2$ concentration and contact time. The introduction of water into reactant feed decreased the catalytic activity.

• Journal of the Korean Ceramic Society
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• v.30 no.11
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• pp.925-932
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• 1993

The perovskite phase in PZN-PMN-PT (Pb(Zn, Mg)1/3Nb2/3O3-PbTiO3) pseudoternary ceramics was stabilized by the addition of excess constituent divalent oxides (PbO, MgO and ZnO). The excess addition of 5mol% MgO or 7.5mol% PbO fully stabilized the perovskite phase. The enhanced diffuse phase transition (DPT) and the decrease in the electrical resistivity observed in the presence of excess ZnO or MgO were interpreted in terms of the additional formation of negatively charged, short-range ordered 1:1 domains with a concomitant generation of charge carriers, holes.

• Transactions of the Korean Society of Automotive Engineers
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• v.9 no.3
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• pp.68-75
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• 2001

In this paper, a number of supported metal oxides and perovskite type catalysts were investigated for the NOx reduction from the diesel engine exhaust gas. All catalysts were made into pellets type with diameter of 3-4 mm alumina(Al$_2$O$_3$) as a supporter. These samples were tested by real diesel exhaust gas which contains CO, hydrocarbons and soot in the temperature range of 150~55$0^{\circ}C$ with the $3300h^{-1}$ space velocity (SV). Among the results, several promising catalysts showed NOx conversion above 50% in the temperature range of 150-35$0^{\circ}C$. From these results supported metal oxides catalysts and perovskite type could be recommended for the practical application to the automobile exhaust treatments.

• Proceedings of the Materials Research Society of Korea Conference
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• 2007.11a
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• pp.25.1-25.1
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• 2007

• Bulletin of the Korean Chemical Society
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• v.26 no.10
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• pp.1591-1596
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• 2005

• Journal of the Korean Electrochemical Society
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• v.10 no.2
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• pp.116-125
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• 2007

This article is concerned with synthesis, characterisation and electrochemical application of the mixed conducting perovskite type oxide to electrode materials for solid oxide fuel cell. First, this review provides a comprehensive survey of the various synthetic methods such as solid state reaction, Pechini, glycine nitrate process and sol-gel methods for the preparation of perovskite type oxide powders. Subsequently, the electrical and microstructural properties of the mixed conducting oxides were discussed in detail. Finally, as electrochemical applications of the mixed conducting perovskite type oxides to electrode materials for solid oxide fuel cell, fundamentals of theoretical ac-impedance model for porous mixed conducting electrodes were introduced. Furthermore, the ac-impedance behaviour of porous and dense mixed conducting electrodes prepared by various synthetic methods was discussed.

• Bulletin of the Korean Chemical Society
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• v.18 no.9
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• pp.972-976
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• 1997

Single phase ruthenium oxides with perovskite (ATi1-xRuxO3 (A=Ca, Sr)) and pyrochlore structure (Bi2Ru2O7, Pb2Ru2O6.5) have been prepared reproducibly by solid state reaction methods and their electrocatalytic activities for oxygen evolution have been examined by Tafel plots. Tafel slopes vary from a low value of 42 mV/decade up to 222 mV/decade at room temperature. The high exchange current densities and high Tafel slopes compared with those obtained from the RuO2 DSA electrode at the crystalline single phase metal oxide electrodes suggest that they are better electrocatalysts at low overpotentials. A favorable change in the Tafel slope for the oxygen evolution reaction occurs as the ruthenium content increases. Substitution of Ti for Ru in the perovskite solid solutions enhanced their chemical stability by losing marginal electrochemical activity.