In an attempt to utilize ozone effectively, a series of praseodymium-modified γ-Al 2 O 3 (Pr/Al 2 O 3 ) was prepared via incipient wetness impregnation using Pr(NO 3 ) 3 ·6H 2 O as the precursor. The structure and properties of the catalysts were studied by X-ray diffraction (XRD) and the Brunauer−Emmett−Teller (BET) method. Catalytic activity was evaluated by monitoring the degradation of succinic acid (SA) in the presence of ozone. The praseodymium modification can effectively enhance the ozonation activity of γ-Al 2 O 3 upon SA removal. Increasing the calcination temperature of Pr/Al 2 O 3 is disadvantageous for the catalytic process, whereas increasing the load of praseodymium is helpful. After three successive cycles, the Pr/Al 2 O 3 catalyst remained stable in the catalytic ozonation of SA. Overall, the initial degradation rate of SA, as well as the saturated adsorption capacity of SA, were found to have a linear relation to changes of the surface hydroxyl groups of the catalyst. On this basis, we conclude that the significant enhancement of SA degradation using Pr/Al 2 O 3 as a catalyst should be because praseodymium, in the form of Pr 6 O 11, promoted the formation of surface hydroxyl groups. Hence, the adsorption was increased, and the degradation rate of SA was enhanced.
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He et al. (2010) studied this question.
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