New operation strategy for driving the selectivity of NOx reduction to N2, NH3 or N2O during lean/rich cycling of a lean NOx trap catalyst
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22340%2F16%3A43902345" target="_blank" >RIV/60461373:22340/16:43902345 - isvavai.cz</a>
Výsledek na webu
<a href="http://dx.doi.org/10.1016/j.apcatb.2015.09.002" target="_blank" >http://dx.doi.org/10.1016/j.apcatb.2015.09.002</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.apcatb.2015.09.002" target="_blank" >10.1016/j.apcatb.2015.09.002</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
New operation strategy for driving the selectivity of NOx reduction to N2, NH3 or N2O during lean/rich cycling of a lean NOx trap catalyst
Popis výsledku v původním jazyce
Periodical regeneration of NOx storage catalyst (also known as lean NOx trap) by short rich pulses of CO, H2 and hydrocarbons is necessary for the reduction of nitrogen oxides adsorbed on the catalyst surface. Ideally, the stored NOx is converted into N2, but N2O and NH3 by-products can be formed as well, particularly at low-intermediate temperatures. The N2 and N2O products are formed concurrently in two peaks. We propose and demonstrate a novel strategy for driving the selectivity of the secondary peaks towards desired products. It is based on a transition phase of neutral or slightly lean (nearly stoichiometric) character inserted between the rich and the fully lean phase. This strategy allows more complete regeneration of the catalyst with higher N2 yield and without the undesired formation of a secondary N2O peak. Furthermore, NH3 can be formed during this slightly lean transition phase without any CO or hydrocarbons breakthrough. Such ammonia formation is desirable in the exhaust gas aftertreatment systems combining LNT with passive SCR technology.
Název v anglickém jazyce
New operation strategy for driving the selectivity of NOx reduction to N2, NH3 or N2O during lean/rich cycling of a lean NOx trap catalyst
Popis výsledku anglicky
Periodical regeneration of NOx storage catalyst (also known as lean NOx trap) by short rich pulses of CO, H2 and hydrocarbons is necessary for the reduction of nitrogen oxides adsorbed on the catalyst surface. Ideally, the stored NOx is converted into N2, but N2O and NH3 by-products can be formed as well, particularly at low-intermediate temperatures. The N2 and N2O products are formed concurrently in two peaks. We propose and demonstrate a novel strategy for driving the selectivity of the secondary peaks towards desired products. It is based on a transition phase of neutral or slightly lean (nearly stoichiometric) character inserted between the rich and the fully lean phase. This strategy allows more complete regeneration of the catalyst with higher N2 yield and without the undesired formation of a secondary N2O peak. Furthermore, NH3 can be formed during this slightly lean transition phase without any CO or hydrocarbons breakthrough. Such ammonia formation is desirable in the exhaust gas aftertreatment systems combining LNT with passive SCR technology.
Klasifikace
Druh
J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
CEP obor
CI - Průmyslová chemie a chemické inženýrství
OECD FORD obor
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Návaznosti výsledku
Projekt
<a href="/cs/project/LH12086" target="_blank" >LH12086: Analýza, modelování a řízení časoprostorových koncentračních profilů v katalyzátorech pro redukci oxidů dusíku (deNOx) v automobilových výfukových plynech</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2016
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Applied Catalysis B:Environment
ISSN
0926-3373
e-ISSN
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Svazek periodika
182
Číslo periodika v rámci svazku
neuveden
Stát vydavatele periodika
NL - Nizozemsko
Počet stran výsledku
6
Strana od-do
109-114
Kód UT WoS článku
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EID výsledku v databázi Scopus
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