Next Article in Journal
Estimation of the Effectiveness Factor for Immobilized Enzyme Catalysts through a Simple Conversion Assay
Next Article in Special Issue
Structure and Catalytic Behavior of Alumina Supported Bimetallic Au-Rh Nanoparticles in the Reduction of NO by CO
Previous Article in Journal
Organocatalysis and Beyond: Activating Reactions with Two Catalytic Species
Previous Article in Special Issue
Cobalt Oxide Catalysts in the Form of Thin Films Prepared by Magnetron Sputtering on Stainless-Steel Meshes: Performance in Ethanol Oxidation
Open AccessArticle

Deactivation of Cu/SSZ-13 NH3-SCR Catalyst by Exposure to CO, H2, and C3H6

1
Competence Centre for Catalysis (KCK), Chemical Engineering, Chalmers University of Technology, SE-412 96 Göteborg, Sweden
2
Volvo Car Corporation, SE-405 31 Göteborg, Sweden
*
Author to whom correspondence should be addressed.
Catalysts 2019, 9(11), 929; https://doi.org/10.3390/catal9110929
Received: 17 September 2019 / Revised: 27 October 2019 / Accepted: 1 November 2019 / Published: 6 November 2019
(This article belongs to the Special Issue Catalysis for the Removal of Gas-Phase Pollutants)
Lean nitric oxide (NOx)-trap (LNT) and selective catalytic reduction (SCR) are efficient systems for the abatement of NOx. The combination of LNT and SCR catalysts improves overall NOx removal, but there is a risk that the SCR catalyst will be exposed to high temperatures and rich exhaust during the LNTs sulfur regeneration. Therefore, the effect of exposure to various rich conditions and temperatures on the subsequent SCR activity of a Cu-exchanged chabazite catalyst was studied. CO, H2, C3H6, and the combination of CO + H2 were used to simulate rich conditions. Aging was performed at 800 °C, 700 °C, and, in the case of CO, 600 °C, in a plug-flow reactor. Investigation of the nature of Cu sites was performed with NH3-temperature-programed desorption (TPD) and diffuse reflectance infrared Fourier transform spectroscopy (DRIFT) of probe molecules (NH3 and NO). The combination of CO and H2 was especially detrimental to SCR activity and to NH3 oxidation. Rich aging with low reductant concentrations resulted in a significantly larger deactivation compared to lean conditions. Aging in CO at 800 °C caused SCR deactivation but promoted high-temperature NH3 oxidation. Rich conditions greatly enhanced the loss of Brønsted and Lewis acid sites at 800 °C, indicating dealumination and Cu migration. However, at 700 °C, mainly Brønsted sites disappeared during aging. DRIFT spectroscopy analysis revealed that CO aging modified the Cu2+/CuOH+ ratio in favor of the monovalent CuOH+ species, as opposed to lean aging. To summarize, we propose that the reason for the increased deactivation observed for mild rich conditions is the transformation of the Cu species from Z2Cu to ZCuOH, possibly in combination with the formation of Cu clusters.
Keywords: Cu/SSZ-13; NH3 SCR; aging; deactivation; rich conditions Cu/SSZ-13; NH3 SCR; aging; deactivation; rich conditions
Show Figures

Graphical abstract

MDPI and ACS Style

Auvray, X.; Mihai, O.; Lundberg, B.; Olsson, L. Deactivation of Cu/SSZ-13 NH3-SCR Catalyst by Exposure to CO, H2, and C3H6. Catalysts 2019, 9, 929.

Show more citation formats Show less citations formats
Note that from the first issue of 2016, MDPI journals use article numbers instead of page numbers. See further details here.

Article Access Map by Country/Region

1
Back to TopTop