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首页> 外文期刊>Chemical engineering journal >Synergy of KCl and Hg-el on selective catalytic reduction of NO with NH3 over V2O5-WO3/TiO2 catalysts
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Synergy of KCl and Hg-el on selective catalytic reduction of NO with NH3 over V2O5-WO3/TiO2 catalysts

机译:KCl和Hg-el在V2O5-WO3 / TiO2催化剂上用NH3选择性催化还原NO的协同作用

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摘要

The synergy effects of KCl and Hg-el on selective catalytic reduction of NO with NH3 over V2O5-WO3/TiO2 catalysts were studied. KCl was doped by impregnation, and Hgel was added by dry-gas adsorption method. Catalytic activity was tested under the condition of simulated flue gas. XRD, SEM, BET, FT-IR, NH3-TPD and NH3 chemisorption were used to characterize the changes of the phase composition, microstructure, surface acidity and functional groups. Deactivation was observed obviously for the catalysts of KCl loadings, while Hg-el showed weakly negative effect. KCl caused agglomeration to the catalysts, but Hg-el did not. For KCl poisoning catalysts, Bronsted acid sites were neutralized evidently and it was related to the KCl loading amounts. KCl could react with V-OH to ultimately form -V-O-K and Cl-V-O-K, resulting in the deactivation of the active sites substantially. Synergy effect was observed that Hgel could increase the amount of chemisorbed NH3 and retard the deactivation caused by KCl. Hg-el would combine with Cl that introduced from KCl to form HgCl or HgCl2, and partly replace K. Then, -V-O center dot center dot center dot Hg or -V-O-Hg-Cl produced, causing the amount of adsorbed NH3 increased due to their competition for the active sites. Based on the experimental results and theoretical analysis, the probable synergy mechanism model of KCl and Hg-el poisoning V2O5-WO3/TiO2 catalysts was proposed. (C) 2014 Elsevier B.V. All rights reserved.
机译:研究了KCl和Hg-el对V2O5-WO3 / TiO2催化剂上的NH3选择性催化还原NO的协同作用。通过浸渍来掺杂KCl,并且通过干气吸附法添加Hgel。在模拟烟气条件下测试了催化活性。用XRD,SEM,BET,FT-IR,NH3-TPD和NH3化学吸附法表征了相组成,微观结构,表面酸度和官能团的变化。氯化钾负载量的催化剂明显失活,而汞汞显示出弱的负作用。 KCl引起了催化剂的团聚,但是Hg-el却没有。对于氯化钾中毒催化剂,布朗斯台德酸位明显被中和,这与氯化钾的负载量有关。 KCl可以与V-OH反应,最终形成-V-O-K和Cl-V-O-K,从而导致活性位点基本上失活。观察到协同作用,Hgel可以增加化学吸附的NH3的量并延迟KCl引起的失活。 Hg-el与从KCl引入的Cl结合形成HgCl或HgCl2,并部分替代K。然后,生成-VO中心点中心点中心点Hg或-VO-Hg-Cl,导致吸附的NH3量增加他们对活跃网站的竞争。基于实验结果和理论分析,提出了KCl和Hg-el中毒V2O5-WO3 / TiO2催化剂的协同作用机理模型。 (C)2014 Elsevier B.V.保留所有权利。

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