Catalytic activity of MnOx/TiO2 catalysts synthesized with different manganese precursors for the selective catalytic reduction of nitrogen oxides

被引:14
作者
Hwang, Sungchul [1 ]
Jo, Seung-Hyeon [2 ]
Kim, Janghoon [3 ]
Shin, Min-Chul [4 ]
Chun, Ho Hwan [5 ]
Park, Hyun [6 ]
Lee, Heesoo [2 ]
机构
[1] Pusan Natl Univ, Grad Sch Convergence Sci, Busan 609735, South Korea
[2] Pusan Natl Univ, Sch Mat Sci & Engn, Busan 609735, South Korea
[3] POSCO, Tech Res Labs, Pohang Res Lab, Pohang 790300, South Korea
[4] Korea Testing Lab, Mat Technol Ctr, Seoul 152718, South Korea
[5] Pusan Natl Univ, Dept Naval Architecture & Ocean Engn, Busan 609735, South Korea
[6] Pusan Natl Univ, Global Core Res Ctr Ships & Offshore Plants, Busan 609735, South Korea
基金
新加坡国家研究基金会;
关键词
MnOx/TiO2; Manganese precursor; de-NOx efficiency; Surface valence state; LOW-TEMPERATURE SCR; NO; NH3; SURFACE; MECHANISM; VANADIA; MNOX/AL2O3; HYDROGEN; AMMONIA; CR;
D O I
10.1007/s11144-015-0948-7
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The effects of different manganese precursors on the low-temperature (100-300 A degrees C) selective catalytic reduction of nitrogen oxide (NOx) were investigated. MnOx/TiO2 catalysts were prepared by a sol-gel method using three different precursors, manganese(II) nitrate (MN), manganese(II) acetate (MA2), and manganese(III) acetate (MA3). They had an overall high specific surface area, but the relatively small surface areas of MN-MnOx/TiO2 and MA3-MnOx/TiO2 were due to the existence of a Mn3O4 phase in these catalysts. There is no chemical reaction at the working temperature, which proves the high thermal stability of all the catalysts. The result of de-NOx (removal of NOx) efficiency in the low temperature region showed that the catalyst synthesized with manganese acetate had higher catalytic activity than the catalyst synthesized with manganese nitrate. Despite the relatively small surface area, the MA3-MnOx/TiO2 exhibited the highest de-NOx efficiency, which resulted from the most enriched Mn concentration and Mn4+ species (MnO2) as well as strong acid sites on catalyst surface.
引用
收藏
页码:583 / 591
页数:9
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