To develop a highly reactive and easily regenerable zinc oxide high-temperature desulfurization sorbent, a modification of ZnO−TiO2 by addition of ZrO2 was studied. The metal oxides ZnO−TiO2−ZrO2 were prepared by a coprecipitation method:  the amount of ZnO was a fixed 50 mol % of the sample. In this study, it was found that the addition of 5 or 10 mol % ZrO2 to 50 mol % ZnO−50 mol % TiO2 greatly improved the reactivity for H2S removal. Furthermore, the addition of ZrO2 improved its regenerability: the temperature for the regeneration of the sample was decreased to ca. 40 °C in the absence of H2O and ca. 75 °C in the presence of 10% H2O by the addition of 10% ZrO2.

To understand the contribution of lime to the abatement of N2O emission from fluidized coal combustor, the catalytic activity of the lime for the decomposition of N2O under coal combustion conditions was studied. Lime was active for the catalytic decomposition of N2O, and its activity was stable in the simulated coal combustion flue gas in the absence of SO2 at 800 °C. The catalytic activity of lime was depressed by the presence of CO2, H2O, and SO2. The affect of the presence of SO2 seemed to be most important:  the catalytic activity of the lime gradually decreased as the degree of sulfation increased, and the specific surface area decreased with the progression of sulfation. From N2O pretreatment and temperature-programmed desorption studies on the used lime, it was found that two oxygen species and one species of NO desorbed. A surface character change due to sulfation is expected from these gas desorptions. From the relation of the activity to the surface area or the desorption of the gases or both, it was concluded that a decrease in the surface area contributed to the decay of the activity more effectively than the surface character change caused by the sulfation.