Abstract

Carbon-modified alumina-supported copper oxide catalysts have been investigated. The samples have been prepared by modified incipient techniques. The γ-Al 2O 3-supported carbon phase permits sufficient modification of the chemical nature of the support surface in the region of low carbon contents without changing the specific surface area and the mesoporous character of the samples as compared to those of initial γ-Al 2O 3. In addition, the surface oxygen groups of the carbon phase, similar to the hydroxyl groups of the alumina surface, affect the formation and type of copper oxide phase. It has been established that the catalysts investigated have high activity in the reduction of NO with CO, the highest activity belonging to the Cu17AC/AL catalyst, which contains the largest amount of carbon. This sample is also active with respect to the direct decomposition of NO.

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