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Suppression of the oxygen storage and release kinetics in Ce0.5Zr0.5O2 induced by P, Ca and Zn chemical poisoning

Paper ID Volume ID Publish Year Pages File Format Full-Text
47050 46457 2011 11 PDF Available
Title
Suppression of the oxygen storage and release kinetics in Ce0.5Zr0.5O2 induced by P, Ca and Zn chemical poisoning
Abstract

The present investigation concerns for the first time the understanding of the individual and combined effects of phosphorous with calcium or zinc deposited on a Ce0.5Zr0.5O2 solid followed by calcination in 20%O2/He at 850 °C, on the kinetics of oxygen storage and release of the thus derived contaminated Ce0.5Zr0.5O2 solids. Towards this aim, physicochemical and redox properties of Ce0.5Zr0.5O2, P/Ce0.5Zr0.5O2, P–Ca/Ce0.5Zr0.5O2 and P–Zn/Ce0.5Zr0.5O2 solids were investigated by means of BET, XRD, SEM, XPS, TPR, OSC and TPIE techniques. P, Ca or Zn deposition on Ce0.5Zr0.5O2 solid was found to result in a drastic decrease in the population of reactive oxygen species present on the surface and within the subsurface/bulk region of the solid. The latter is attributed to the formation of cerium and calcium phosphates in the subsurface region of the solid, as well as to the formation of zinc oxide on the surface of the solid, clogging pores lower than 10 nm in size as revealed by BJH pores size distribution measurements. Another reason for the severe reduction in the OSC (up to 70%) of contaminated by phosphorous Ce0.5Zr0.5O2 solid is the rearrangement of its surface composition resulting in the lowering of the Ce/Zr surface ratio. The latter is linked to the lowering of the concentration of reactive oxygen associated with the strength of Ce–O–Zr bonding. The incorporation of P within the subsurface region of Ce0.5Zr0.5O2 crystals and its reaction with the solid producing CePO4 causes the formation of a significant amount of Ce3+ which is very difficult to get re-oxidised, and locks the Ce(III)/Ce(IV) redox couple. Phosphorus incorporation within the subsurface/bulk of Ce0.5Zr0.5O2 solid oxide particles was found to significantly increase the activation energy of bulk oxygen diffusion from 126.5 to ∼169.0 kJ mol−1, while the concurrent deposition of Ca or Zn along with P was found to strongly suppress surface oxygen diffusion.

Graphical abstractEffects of P, P–Ca and P–Zn deposition on the surface of Ce0.5Zr0.5O2 solid solution followed by calcination at 850 °C on the surface and bulk oxygen diffusion kinetics and OSC quantity.Figure optionsDownload full-size imageDownload as PowerPoint slideHighlights► P (4.5 wt%) deposition on Ce0.5Zr0.5O2 solid solution reduces significantly OSC. ► P–Zn co-deposition on Ce0.5Zr0.5O2 gives higher OSC than P deposition alone. ► P deposition on Ce0.5Zr0.5O2 followed by calcination at 850 °C forms CePO4. ► CePO4 locks the Ce4+/Ce3+ redox couple and increases Eb for bulk O2− diffusion. ► P–Ca and P–Zn deposition on Ce0.5Zr0.5O2 strongly inhibits surface On− diffusion.

Keywords
TWC deactivation; Ceria–zirconia; Chemical poisoning; OSC; Oxygen isotopic exchange; TPIE
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Suppression of the oxygen storage and release kinetics in Ce0.5Zr0.5O2 induced by P, Ca and Zn chemical poisoning
Publisher
Database: Elsevier - ScienceDirect
Journal: Applied Catalysis B: Environmental - Volume 106, Issues 1–2, 21 July 2011, Pages 103–113
Authors
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Subjects
Physical Sciences and Engineering Chemical Engineering Catalysis