期刊
CHEMICAL ENGINEERING JOURNAL
卷 459, 期 -, 页码 -出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2023.141614
关键词
P-modified; VW/Ti catalyst; Dip-calcination method; P loading; SO2 oxidation; NH3-SCR
This study investigates the effect of phosphorus addition on the activity of NOx conversion and SO2 oxidation over VW/Ti catalyst. The results show that the P-modified VW/Ti catalyst not only enhances the catalytic activity at low temperature, but also reduces the oxidation rate of SO2. The 1.5PVW/Ti catalyst exhibits the lowest SO2 oxidation rate at 360 degrees C and achieves about 30% reduction in SO2 oxidation rate compared to the 0PVW/Ti catalyst, while the conversion of NOx is still above 95%.
Commercial VW/Ti catalyst used in selective catalytic reduction (SCR) process is one of the major sources of SO3 in coal-fired boiler, and modification of VW/Ti catalyst by adding catalytic promoter has been demonstrated to be an effective way to inhibit SO3 generation. In this study, the effect of P addition on the activity of NOx conversion and SO2 oxidation over VW/Ti catalyst was investigated. The results showed that the P-modified VW/Ti catalyst not only enhanced the catalytic activity at low temperature, but also reduced the oxidation rate of SO2. The 1.5PVW/Ti catalyst exhibited the lowest SO2 oxidation rate at 360 degrees C and achieved about 30 % reduction in SO2 oxidation rate when compared to 0PVW/Ti catalyst, whereas the conversion of NOx was still above 95 %. The physicochemical properties of catalysts were comprehensively characterized with N-2 adsorption, XRD, H-2-TPR, NH3-TPD, XPS and DRIFTS. The results illustrated that the W-O-W structure was also the main reason for SO2 oxidation on P-modified VW/Ti catalyst, which oxidized SO2 to form intermediate products HSO4- and constantly replenished in the presence of O-2. The oxidation of SO2 was weakened by the generation of VOPO4 on P-modified VW/Ti catalyst surface, which inhibited the formation of VOSO4 by reducing the adsorption of SO2 on the catalyst. In addition, the release of P-OH and W=O were promoted with the addition of P, which led to a significant increase in the intensity of the Bronsted and Lewis acid sites, resulting in the increase in the conversion of NOx at low temperatures.
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