首页> 美国卫生研究院文献>ACS Omega >Annealing Strategies for the Improvement of Low-TemperatureNH3-Selective Catalytic Reduction Activity of CrMnOx Catalysts
【2h】

Annealing Strategies for the Improvement of Low-TemperatureNH3-Selective Catalytic Reduction Activity of CrMnOx Catalysts

机译:改善低温的退火策略CrMnOx催化剂的NH3-选择性催化还原活性

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Annealing strategies for the citrate complexation–combustion method have been explored as a simple approach for improving the catalytic activity of mixed Cr–Mn oxides for the NH3-selective catalytic reduction of NOx. Materials prepared at 300 and 400 °C possess largely amorphous structures, consistent with highly dispersed Cr/Mn components. Annealing at 300 °C for 10 h facilitates the formation of catalysts possessing the largest surface area, reducibility, acidity, and activity window (92–239 °C), while areal activity is measured at 3.8 nmol s–1 m–2 and is comparable to values obtained for materials prepared at 400 °C. Conversely, shorter annealing times of 1 and 5 h at 300 °C produce materials that transform NOx about 2–3 times faster at equivalent surface area. Characterization demonstrates that simple annealing strategies have significant impact on the physiochemical and textural properties of these materials. Moreover, reducibility,Oα species, and acidity were correlated against arealactivity, but only the latter exhibited a near-linear correlation,indicating its dominance in controlling surface reaction rates.
机译:已经探索了柠檬酸盐络合燃烧法的退火策略,作为提高混合Cr-Mn氧化物对NH3选择性催化还原NOx的催化活性的简单方法。在300和400°C下制备的材料主要具有非晶态结构,与高度分散的Cr / Mn成分一致。在300°C退火10 h有助于形成具有最大表面积,还原度,酸度和活性范围(92–239°C)的催化剂,而在3.8 nmol s –1 下测定的面活性。 sup> m –2 ,与在400°C下制备的材料所获得的值相当。相反,在300°C下较短的1和5 h退火时间产生的材料在相等的表面积下转化NOx的速度大约快2-3倍。表征表明,简单的退火策略对这些材料的物理化学和质地特性有重大影响。而且,还原性Oα种类和酸度与面积相关活动,但只有后者表现出接近线性的相关性,表明它在控制表面反应速率方面占主导地位。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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