Institute for Integrated Catalysis, Pacific Northwest National Laboratory, P.O. Box 999, Richland, WA, 99354, USA.
Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, P.O. Box 999, Richland, WA, 99354, USA.
Nat Commun. 2019 Mar 8;10(1):1137. doi: 10.1038/s41467-019-09021-3.
Commercial Cu/SAPO-34 selective catalytic reduction (SCR) catalysts have experienced unexpected and quite perplexing failure. Understanding the causes at an atomic level is vital for the synthesis of more robust Cu/SAPO-34 catalysts. Here we show, via application of model catalysts with homogeneously dispersed isolated Cu ions, that Cu transformations resulting from low-temperature hydrothermal aging and ambient temperature storage can be semi-quantitatively probed with 2-dimensional pulsed electron paramagnetic resonance. Coupled with kinetics, additional material characterizations and DFT simulations, we propose the following catalyst deactivation steps: (1) detachment of Cu(II) ions from cationic positions in the form of Cu(OH); (2) irreversible hydrolysis of the SAPO-34 framework forming terminal Al species; and (3) interaction between Cu(OH) and terminal Al species forming SCR inactive, Cu-aluminate like species. Especially significant is that these reactions are greatly facilitated by condensed water molecules under wet ambient conditions, causing low temperature failure of the commercial Cu/SAPO-34 catalysts.
商用 Cu/SAPO-34 选择性催化还原 (SCR) 催化剂出现了意想不到且令人费解的失效现象。在原子水平上理解其失效原因对于合成更稳定的 Cu/SAPO-34 催化剂至关重要。在这里,我们通过使用具有均匀分散孤立 Cu 离子的模型催化剂表明,低温水热老化和环境温度储存导致的 Cu 转化可以通过二维脉冲电子顺磁共振进行半定量探测。结合动力学、其他材料特性和 DFT 模拟,我们提出了以下催化剂失活步骤:(1)Cu(II) 离子以 Cu(OH) 的形式从阳离子位置上脱离;(2)SAPO-34 骨架不可逆水解形成末端 Al 物种;(3)Cu(OH) 和末端 Al 物种相互作用形成 SCR 失活的、类铜铝酸盐的物种。特别重要的是,在潮湿的环境条件下,这些反应在凝聚水分子的作用下大大加速,导致商用 Cu/SAPO-34 催化剂在低温下失效。