RWTH Aachen University, Institute of Inorganic Chemistry, Landoltweg 1, D-52056 Aachen, Germany.
Beilstein J Nanotechnol. 2012;3:667-73. doi: 10.3762/bjnano.3.76. Epub 2012 Sep 26.
In a proof-of-concept study we demonstrate in situ reaction monitoring of DeNO(x)-SCR on proton-conducting zeolites serving as catalyst and gas sensor at the same time. By means of temperature-dependent impedance spectroscopy we found that the thermally induced NH(3) desorption in H-form and in Fe-loaded zeolite H-ZSM-5 follow the same process, while a remarkable difference under DeNO(x)-SCR reaction conditions was found. The Fe-loaded catalyst shows a significantly lower onset temperature, and time-dependent measurements suggest different SCR reaction mechanisms for the two catalysts tested. These results may help in the development of catalysts for the reduction of NO(x) emissions and ammonia consumption, and provide insight into the elementary catalytic process promoting a full description of the NH(3)-SCR reaction system.
在一项概念验证研究中,我们展示了在质子传导沸石上同时作为催化剂和气体传感器的 DeNO(x)-SCR 的原位反应监测。通过与温度相关的阻抗谱,我们发现 H 型和负载 Fe 的沸石 H-ZSM-5 中的热诱导 NH(3)解吸遵循相同的过程,而在 DeNO(x)-SCR 反应条件下存在显著差异。负载 Fe 的催化剂表现出明显更低的起始温度,并且时变测量表明两种催化剂的 SCR 反应机制不同。这些结果可能有助于开发用于减少 NO(x)排放和氨消耗的催化剂,并深入了解促进完整描述 NH(3)-SCR 反应体系的基本催化过程。