scispace - formally typeset
Journal ArticleDOI

A review of the selective reduction of NOx, with hydrocarbons under lean-burn conditions with non-zeolitic oxide and platinum group metal catalysts

Reads0
Chats0
TLDR
In this paper, it is concluded that although there is indirect, mainly spectroscopic, evidence for various reaction intermediates on the catalyst surface, it is difficult to confirm that any of these are involved in a critical mechanistic step because of a lack of a direct quantitative correlation between infrared and kinetic measurements.
Abstract
Research on the selective reduction of NOx with hydrocarbons under lean-burn conditions using non-zeolitic oxides and platinum group metal (PGM) catalysts has been critically reviewed. Alumina and silver-promoted alumina catalysts have been described in detail with particular emphasis on an analysis of the various reaction mechanisms that have been put forward in the literature. The influence of the nature of the reducing agent, and the preparation and structure of the catalysts have also been discussed and rationalised for several other oxide systems. It is concluded for non-zeolitic oxides that species that are strongly adsorbed on the surface, such as nitrates/nitrites and acetates, could be key intermediates in the formation of various reduced and oxidised species of nitrogen, the further reaction of which leads eventually to the formation of molecular nitrogen. For the platinum group metal catalysts, the different mechanisms that have been proposed in the literature have been critically assessed. It is concluded that although there is indirect, mainly spectroscopic, evidence for various reaction intermediates on the catalyst surface, it is difficult to confirm that any of these are involved in a critical mechanistic step because of a lack of a direct quantitative correlation between infrared and kinetic measurements. A simple mechanism which involves the dissociation of NO on a reduced metal surface to give N(ads) and O(ads), with subsequent desorption of N2 and N2O and removal of O(ads) by the reductant can explain many of the results with the platinum group metal catalysts, although an additional contribution from organo-nitro-type species may contribute to the overall NOx reduction activity with these catalysts. It is concluded, after the investigation of hundreds of catalyst formulations, that many of the fundamental questions relating to lean deNOx reactions have been addressed and the main boundary conditions have been established. It seems clear that catalysts with sufficient activity, selectivity or stability to satisfy the demanding conditions that appertain in automotive applications are still far away. The rapidly growing interest in NOx storage systems reflects this situation, and it now seems to be the case that acceptable direct NOx reduction catalysts may be very difficult to find for lean-burn applications.

read more

Citations
More filters
Journal ArticleDOI

Overview of the Fundamental Reactions and Degradation Mechanisms of NOx Storage/Reduction Catalysts

TL;DR: In this article, the authors describe the work carried out in characterizing, developing, and understanding this catalyst technology for application in mobile exhaust gas aftertreatment, which includes five general steps involved in NOx reduction to N2 on NSR catalysts; NO oxidation, NO2 and NO sorption leading to nitrite and nitrate species.
Journal ArticleDOI

Gas-phase catalysis by atomic and cluster metal ions: the ultimate single-site catalysts.

TL;DR: This Review describes how transfer of oxygen atoms, bond activation, and coupling of fragments can be mediated by atomic or cluster metal ions, and improves the understanding of the intrinsic operation of a practical catalyst at a strictly molecular level.
Journal ArticleDOI

Catalytic NOx Abatement Systems for Mobile Sources: From Three-Way to Lean Burn after-Treatment Technologies

TL;DR: Catalytic NOx Abatement Systems for Mobile Sources: From Three-Way to Lean Burn after-Treatment Technologies is presented.
Journal ArticleDOI

Catalysis for NOx abatement

TL;DR: In this paper, the main portion of the review discusses the progress and development of various catalysts for NOx removal from exhaust by NO decomposition, NO reduction by CO or H-2 or NH3 or hydrocarbons.
References
More filters
Journal ArticleDOI

Catalytic removal of NO

TL;DR: In this paper, the authors review the catalytic reactions for the removal of NO and discuss the reduction of NO in the presence of NH3, CO, H-2 or hydrocarbons as well as the decomposition of NO.
Journal ArticleDOI

Activity and durability of Fe/ZSM-5 catalysts for lean burn NOx reduction in the presence of water vapor

TL;DR: In this article, a novel method for the preparation of superior Fe/ZSM-5 catalysts is described, where FeCl 3 is sublimed into the cavities of H 2 -TPR, where it reacts chemically with the acid sites of the zeolite.
Journal ArticleDOI

The current state of research on automotive lean NOx catalysis

TL;DR: In this article, three principal types of catalysts active for HC-SCR are discussed, and a review of their performance is provided with the goal of assisting researchers in their assessment of catalytic performance.
Journal ArticleDOI

Mechanistic Aspects of the Selective Reduction of NO by Propene over Alumina and Silver–Alumina Catalysts

TL;DR: In this paper, the selective catalytic reduction of NO with C3H6 in the presence of a large excess of O2 was studied over γ-Al2O3 and the lowloading silver material exhibited high conversions to N2 whereas the highloading sample predominantly yielded N2O.
Journal ArticleDOI

Mechanism of the selective reduction of nitrogen monoxide on platinum-based catalysts in the presence of excess oxygen

TL;DR: A range of alumina-supported platinum catalysts have been prepared and investigated for the selective reduction of nitrogen monoxide in the presence of a large excess of oxygen in steady state microreactor experiments.
Related Papers (5)
Trending Questions (1)
How to confirm a substance as a catalyst by quantitative analysis?

It is concluded that although there is indirect, mainly spectroscopic, evidence for various reaction intermediates on the catalyst surface, it is difficult to confirm that any of these are involved in a critical mechanistic step because of a lack of a direct quantitative correlation between infrared and kinetic measurements.