Key Laboratory of Advanced Materials of Ministry of Education, School of Materials Science and Engineering, Tsinghua University, Beijing 100084, China.
Key Laboratory of Advanced Materials of Ministry of Education, School of Materials Science and Engineering, Tsinghua University, Beijing 100084, China; Yangtze Delta Region Institute of Tsinghua University, Jiaxing 314006, China.
J Environ Sci (China). 2017 Jul;57:110-117. doi: 10.1016/j.jes.2016.12.001. Epub 2016 Dec 6.
Sulfur poisoning of VO/BaSO-TiO (VBT), VO/WO-TiO (VWT) and VO/BaSO-WO-TiO (VBWT) catalysts was performed in wet air at 350°C for 3hr, and activities for the selective catalytic reduction of NO with NH were evaluated for 200-500°C. The VBT catalyst showed higher NO conversions after sulfur poisoning than the other two catalysts. The introduction of barium sulfate contributed to strong acid sites for the as-received catalyst, and eliminated the redox cycle of active vanadium oxide to some extent, which resulted in a certain loss of activity. Readily decomposable sulfate species formed on VBT-S instead of inactive sulfates on VWT-S. These decomposable sulfates increased the number of strong acid sites significantly. Some sulfate species escaped during catalyst preparation and barium sulfate was reproduced during sulfur poisoning, which protects vanadia from sulfur oxide attachment to a great extent. Consequently, the VBT catalyst exhibited the best resistance to sulfur poisoning.
在 350°C 的湿空气中对 VO/BaSO-TiO(VBT)、VO/WO-TiO(VWT)和 VO/BaSO-WO-TiO(VBWT)催化剂进行了硫化处理,在 200-500°C 下评估了它们用于选择性催化还原 NO 与 NH 的活性。与另外两种催化剂相比,硫化后的 VBT 催化剂具有更高的 NO 转化率。硫酸钡的引入为原始催化剂提供了强酸位,并在一定程度上消除了活性氧化钒的氧化还原循环,导致活性的一定损失。VBT-S 上形成了易分解的硫酸盐物种,而不是 VWT-S 上的非活性硫酸盐。这些可分解的硫酸盐显著增加了强酸位的数量。在催化剂制备过程中,一些硫酸盐物种逸出,而在硫化处理过程中又重新生成了硫酸钡,这在很大程度上保护了氧化钒免受二氧化硫的附着。因此,VBT 催化剂表现出了最好的抗硫化中毒能力。