...
首页> 外文期刊>Aerosol and Air Quality Research >In Situ DRIFTS Study of the Low Temperature Selective Catalytic Reduction of NO with NH3 over MnOx Supported on Multi-Walled Carbon Nanotubes Catalysts
【24h】

In Situ DRIFTS Study of the Low Temperature Selective Catalytic Reduction of NO with NH3 over MnOx Supported on Multi-Walled Carbon Nanotubes Catalysts

机译:多壁碳纳米管催化剂上负载的MnOx上NH3低温选择性催化还原NO的原位DRIFTS研究

获取原文
           

摘要

MnOx supported on multi-walled carbon nanotubes (MWCNTs) catalysts were prepared by the pore volume impregnation method and used for low-temperature selective catalytic reduction (SCR) of NO with NH3. Based on the previous study, 10 wt.% loading MnOx/MWCNTs were then selected for investigation of the reaction mechanism by in situ Diffuse Reflectance Infrared Fourier Transform spectroscopy (in-situ DRIFTS). The important intermediates in the SCR of NOx process at 210°C were discussed based on the DRIFTS results. Furthermore, the NH3-SCR reaction pathways over MnOx/MWCNTs catalysts were proposed. The results showed that NH4+ species on Br?nsted acid sites and coordinate ammonia species on Lewis acid sites existed during the SCR reaction. NH4+ species was more active than coordinate ammonia species over the catalysts at 210°C. Most of NOx ad-species would react with NH3 ad-species. However, nitrite species, bidentate and monodentate nitrates contributed to the SCR reaction over the catalysts mostly. Two possible reaction pathways were proposed. One was that NOx ad-species could react with NH4+ to form intermediate of NH4N2O4 (a), NH4NO2 (a) or NH4NO3 (a), then to produce N2 and H2O as the final products. The other pathway was that NH3 was initially adsorbed on active site and NH2 was formed, then NH2 reacted with NOx ad-species to produce intermediate NH2NO2 or NH2NO3 which were unstable and would decompose into N2 and H2O.
机译:通过孔体积浸渍法制备了负载在多壁碳纳米管(MWCNTs)催化剂上的MnOx,并将其用于NH 3的NO低温选择性催化还原(SCR)。基于先前的研究,然后选择10 wt。%负载的MnOx / MWCNT,通过原位漫反射红外傅里叶变换光谱法(原位DRIFTS)研究反应机理。基于DRIFTS结果讨论了210℃下NOx过程SCR中的重要中间体。此外,提出了MnOx / MWCNTs催化剂上的NH3-SCR反应途径。结果表明,SCR反应过程中存在布朗斯台德酸位上的NH4 +和路易斯酸位上的配位氨。在210°C下,催化剂上的NH4 +物种比配位的氨物种更具活性。大多数NOx副物种会与NH3副物种发生反应。然而,亚硝酸盐类,双齿硝酸盐和单齿硝酸盐对SCR反应的贡献主要超过了催化剂。提出了两种可能的反应途径。一种是NOx的种可能与NH4 +反应形成NH4N2O4(a),NH4NO2(a)或NH4NO3(a)的中间体,然后产生N2和H2O作为最终产物。另一个途径是,NH3最初被吸附在活性位上并形成NH2,然后NH2与NOx发生反应生成不稳定的中间体NH2NO2或NH2NO3,并分解为N2和H2O。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号