Selective catalytic reduction of NOx by NH3 at low temperature over manganese oxide catalysts supported on titanate nanotubes

被引:8
|
作者
Camposeco, R. [1 ]
Castillo, S. [2 ]
Rodriguez-Gonzalez, V. [3 ]
Garcia-Serrano, Luz A. [4 ]
Mejia-Centeno, Isidro [3 ]
机构
[1] Univ Nacl Autonoma Mexico, Inst Ciencias Aplicadas & Tecnol, Circuito Exterior S-N, Mexico City, DF, Mexico
[2] Inst Mexicano Petr, Direcc Invest Transformac Hidrocarburos, Mexico City 07730, DF, Mexico
[3] Inst Potosino Invest Cient & Tecnol, Div Mat Avanzados, San Luis Potosi, Slp, Mexico
[4] Inst Politecn Nacl, Ctr Interdisciplinario Invest & Estudios Medio Am, Mexico City, DF, Mexico
关键词
Ammonia; Manganese; Lewis acid sites; SCR-NOx; Sol-gel method; Titanate nanotubes; TITANIUM-DIOXIDE; NITRIC-OXIDE; SCR; PERFORMANCE; MN; MECHANISM;
D O I
10.1080/00986445.2018.1461090
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
We report the NO conversion with NH3 at low temperature over MnOx-supported on titanate nanotubes. The effect of SO2 and water on catalytic activity was also analyzed. For the catalytic activity tests, three catalysts with 1, 3, and 5wt.% of MnOx were synthesized. A high NO conversion (92%) at 180 degrees C is reported for the 1Mn/NTiO2 catalyst. The further addition of MnOx to the support improves the catalytic activity but NO conversion (95%) was shifted to a higher temperature (from 180 to 220 degrees C). However, the presence of SO2 (50ppm) and water (5 vol.%) diminishes the NO conversion up to 60%, which remains after 300min. We found that addition of MnOx increases the Lewis acid sites concentration of the nanotubes. As the Lewis acid sites increase (from 1.86 to 3.56 mu mol m(-2)), the Mn4+/Mn3+ ratio on the surface of the nanotubes decreases (from 4 to 1.6), which indicates that the surface of the catalysts is deficient in electrons. We concluded that a high Lewis acid sites concentration and a low Mn4+/Mn3+ ratio, hence a surface deficient in electrons, improves the catalytic activity to remove NO on the Mn/NTiO2 catalysts.
引用
收藏
页码:1583 / 1593
页数:11
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