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首页> 外文期刊>Applied Catalysis, B. Environmental: An International Journal Devoted to Catalytic Science and Its Applications >MnOx supported on Fe-Ti spinel: A novel Mn based low temperature SCR catalyst with a high N-2 selectivity
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MnOx supported on Fe-Ti spinel: A novel Mn based low temperature SCR catalyst with a high N-2 selectivity

机译:Fe-Ti尖晶石上负载的MnOx:一种新型的具有高N-2选择性的Mn基低温SCR催化剂

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In this work, a novel 10% Mn/Fe-Ti spinel catalyst with an excellent N-2 selectivity was developed for the selective catalytic reduction (SCR) of NO with NH3 at low temperatures. The mechanism of NO reduction and N2O formation over Fe-Ti spinel, 10% Mn/Fe-Ti spinel and 5% Mn-10% Fe/TiO2 was investigated using in situ DRIFT study and the transient reaction study. Meanwhile, the reaction kinetic constant of the SCR reaction (i.e., N-2 formation) through the Eley-Rideal mechanism, the reaction kinetic constant of the SCR reaction through the Langmuir-Hinshelwood mechanism and the reaction kinetic constant of the non selective catalytic reduction (NSCR) reaction (i.e., N2O formation) were obtained according to the steady state kinetic study. They all indicate that the NSCR reaction over 10% Mn/Fe-Ti spinel through the Eley-Rideal mechanism was cut off. NH2 adsorbed on 10% Mn/Fe-Ti spinel can be hardly oxidized to NH as NH2 mainly adsorbed on the support (i.e., Fe-Ti spinel) of 10% Mn/Fe-Ti spinel, which was far away from Mn4+ cations on 10% Mn/Fe-Ti spinel. Therefore, the NSCR reaction over 10% Mn/Fe-Ti spinel through the Eley-Rideal mechanism was suppressed. However, the regeneration of Fe3+ on Fe-Ti spinel was accelerated due to the rapid electron transfer between Mn4+ and Fe2+ on 10% Mn/Fe-Ti spinel resulting in a remarkable promotion on NH3 activation although NH3 adsorbed on 10% Mn/Fe-Ti spinel cannot be directly activated by Mn4+ on 10% Mn/Fe-Ti spinel. Therefore, the SCR reaction over Fe-Ti spinel was promoted remarkably after the load of MnOx. As a result, 10% Mn/Fe-Ti spinel showed an excellent SCR performance especially N-2 selectivity at low temperatures, which was much better than 5% Mn-10% Fe/TiO2 with the same chemical composition. (C) 2015 Elsevier B.V. All rights reserved.
机译:在这项工作中,开发了一种新颖的10%Mn / Fe-Ti尖晶石催化剂,具有出色的N-2选择性,可在低温下用NH3选择性催化还原NO(SCR)。通过原位DRIFT研究和瞬态反应研究,研究了Fe-Ti尖晶石,10%Mn / Fe-Ti尖晶石和5%Mn-10%Fe / TiO2上NO还原和N2O形成的机理。同时,通过Eley-Rideal机理的SCR反应的反应动力学常数(即N-2形成),通过Langmuir-Hinshelwood机理的SCR反应的反应动力学常数和非选择性催化还原的反应动力学常数。根据稳态动力学研究获得(NSCR)反应(即,N 2 O形成)。它们都表明通过Eley-Rideal机理的超过10%Mn / Fe-Ti尖晶石的NSCR反应被切断。吸附在10%Mn / Fe-Ti尖晶石上的NH2几乎不会被氧化成NH,因为NH2主要吸附在10%Mn / Fe-Ti尖晶石的载体(即Fe-Ti尖晶石)上,该载体远离Mn / Fe-Ti尖晶石上的Mn4 +阳离子。 10%Mn / Fe-Ti尖晶石。因此,通过Eley-Rideal机理抑制了超过10%Mn / Fe-Ti尖晶石的NSCR反应。然而,由于在10%Mn / Fe-Ti尖晶石上Mn4 +和Fe2 +之间的快速电子转移,加速了Fe-Ti尖晶石上Fe3 +的再生,尽管NH3吸附在10%Mn / Fe-上,但显着促进了NH3活化。 Ti尖晶石不能被10%Mn / Fe-Ti尖晶石上的Mn4 +直接激活。因此,负载MnOx后,Fe-Ti尖晶石上的SCR反应得到明显促进。结果,10%Mn / Fe-Ti尖晶石表现出优异的SCR性能,尤其是在低温下的N-2选择性,远优于相同化学成分的5%Mn-10%Fe / TiO2。 (C)2015 Elsevier B.V.保留所有权利。

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