Sung Su Kim

Effect of the Mn oxidation state and lattice oxygen in Mn-based TiO2 catalysts on the low-temperature selective catalytic reduction of NO by NH3

TiO2-supported manganese oxide catalysts formed using different calcination temperatures were prepared by using the wet-impregnation method and were investigated for their activity in the low-temperature selective catalytic reduction (SCR) of NO by NH3 with respect to the Mn valence and lattice oxygen behavior. The surface and bulk properties of these catalysts were examined using Brunauer-Emmett-Teller (BET) surface area, X-ray diffraction (XRD), temperature-programmed reduction (TPR), and temperature-programmed desorption (TPD). Catalysts prepared using lower calcination temperatures, which contained Mn4+, displayed high SCR activity at low temperatures and possessed several acid sites and active oxygen. The TPD analysis determined that the Brönsted and Lewis acid sites in the Mn/TiO2 catalysts were important for the low-temperature SCR at 80∼160 and 200∼350 °C, respectively. In addition, the available lattice oxygen was important for attaining high NO to NO2 oxidation at low temperatures. Implications: Recently, various Mn catalysts have been evaluated as SCR catalysts. However, there have been no studies on the relationship of adsorption and desorption properties and behavior of lattice oxygen according to the valence state for manganese oxides (MnOx). Therefore, in this study, the catalysts were prepared by the wet-impregnation method at different calcination temperatures in order to show the difference of manganese oxidation state. These catalysts were then characterized using various physicochemical techniques, including BET, XRD, TPR, and TPD, to understand the structure, oxidation state, redox properties, and adsorption and desorption properties of the Mn/TiO2 catalysts.

Improving the activity of Mn/TiO2 catalysts through control of the pH and valence state of Mn during their preparation

In this study, the authors investigated the influence of the valence state of Mn on the efficacy of selective catalytic reduction using a Mn-based catalyst. The nitrogen oxides (NOx) conversion rate of the catalyst was found to be dependent on the type of TiO2 support employed and on the temperature, as the catalyst showed an excellent conversion of > 80% at a space velocity of 60,000 hr−1 when the temperature was above 200 °C. Brunauer-Emmett-Teller, X-ray diffraction, and X-ray photoelectron spectroscopy analyses confirmed that catalyst displaying the highest activity contained the Mn4+ species and that its valence state was highly dependent on the pH during the catalyst preparation. Implications Recently, various Mn catalysts have been evaluated as selective catalyst reduction (SCR) catalysts. However, in these previous studies, only the reaction characteristics and catalytic activity on the NH3 SCR over Mn catalysts were evaluated. There have been no studies on the effect of pH during catalyst preparation. Therefore, in this study, the effect of pH during the catalyst preparation process was examined and a new application of the Mn catalysts was proposed based on the current findings.

Low Temperature Steam Methane Reforming Over Ni Based Catalytic Membrane Prepared by Electroless Palladium Plating

A Pd/Ni-YSZ porous membrane with different palladium loadings and hydrazine as a reducing reagent was prepared by electroless plating and evaluated for the steam methane reforming activity. The steam-reforming activity of a Ni-YSZ porous membrane was greatly increased by the deposition of 4 g/L palladium in the low-temperature range (600 °C). With an increasing amount of reducing reagent, the Pd clusters were well dispersed on the Ni-YSZ surface and were uniform in size (∼500 nm). The Pd/Ni-YSZ catalytic porous membrane prepared by 1 of Pd/hydrazine ratio possessed an abundant amount of metallic Pd. The optimal palladium loadings and Pd/hydrazine ratio increased the catalytic activity in both the steam-reforming reaction and the Pd dispersion.

Catalytic Performance of Ce0.6Y0.4O2-Supported Platinum Catalyst for Low-Temperature Water–Gas Shift Reaction

In this study, Pt/Ce0.6Y0.4O2 catalyst was prepared using a citric sol–gel method and was used as a catalyst for a water–gas shift (WGS) reaction. Compared to 1 wt % Pt/CeO2 and Pt/Y2O3 catalysts, the Pt/Ce0.6Y0.4O2 catalyst showed a much higher WGS catalytic activity. At 250 °C, the conversion of carbon monoxide was 86.35% at a weight hourly space velocity of 30 000 cm3 gcat–1 h–1. The physicochemical properties of the catalysts were investigated via X-ray diffraction, transmission electron microscopy, chemisorption, H2 and CO temperature-programmed reduction, and in situ diffuse reflection infrared Fourier transform spectroscopy. These results confirmed that the catalytic activity did not depend on the dispersion and particle size of platinum. The high reducibility of the Ce0.6Y0.4O2 support plays a crucial role in improving the activity of the Pt/Ce0.6Y0.4O2 catalyst, and this improvement can also be explained by the reduction in CO adsorption strength.

Physicochemical properties of chars at different treatment temperatures

In this study, the physicochemical properties of the char of Indonesian SM coal following heat treatment at various temperatures were evaluated using X-ray photoelectron spectroscopy (XPS), Fourier-transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), and morphological and specific surface area analysis. Based on these analyses, heat treatment of coal was determined to be the most effective in increasing the coal rank. In the XPS analysis, the C–O and C–O–C groups and quaternary-N species were found to be of a lower grade coal when the pretreatment temperature decreased, meanwhile the C–C group and pyridinic species increased. In the FT-IR analysis, the collapse of the C–O and C–O–C group was observed due to the collapse of the ether group. In SEM and Brunauer–Emmett–Teller (BET) analysis, a decrease in the ether group was shown to be accompanied with the formation of micropores. Implications Recently, XPS analyses have been reported as coal surface analysis. Usually, they have reported the analysis of the coals with different rank. This study investigated the coal surface characteristics of the coals pretreated at different temperature using various analyses (BET, SEM, XPS, FT-IR), and this study can be the basis for other research and applications.