Compositions for passive NOx adsorption (PNA) systems and methods of making and using same

US10086356B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10086356-B2
Application numberUS-201715605750-A
CountryUS
Kind codeB2
Filing dateMay 25, 2017
Priority dateMar 21, 2014
Publication dateOct 2, 2018
Grant dateOct 2, 2018

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  1. Title

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  2. Abstract

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  5. First independent claim

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Abstract

Official abstract text for this publication.

The present disclosure relates to a substrate containing passive NOx adsorption (PNA) materials for treatment of gases, and washcoats for use in preparing such a substrate. Also provided are methods of preparation of the PNA materials, as well as methods of preparation of the substrate containing the PNA materials. More specifically, the present disclosure relates to a coated substrate containing PNA materials for PNA systems, useful in the treatment of exhaust gases. Also disclosed are exhaust treatment systems, and vehicles, such as diesel or gasoline vehicles, particularly light-duty diesel or gasoline vehicles, using catalytic converters and exhaust treatment systems using the coated substrates.

First claim

Opening claim text (preview).

We claim: 1. A method of treating an exhaust gas, comprising: contacting a coated substrate with an exhaust gas comprising NO x emissions, wherein the coated substrate comprises: a substrate; and a Passive NOx Adsorber (PNA) layer comprising nano-sized platinum group metal (PGM) on a plurality of support particles comprising cerium oxide, wherein the amount of cerium oxide used in the PNA layer is from about 50 g/L to about 400 g/L. 2. The method of claim 1 , wherein the PNA layer stores NOx gas up to at least a first temperature and releases the stored NOx gas at or above the first temperature. 3. The method of claim 2 , wherein the first temperature is 150° C. 4. The method of claim 2 , wherein the PGM comprises ruthenium, the PNA layer stores NOx gas up to at least a 300° C. and releases the stored NOx gas at or above 300° C. 5. The method of claim 1 , wherein the plurality of support particles are micron-sized or the plurality of support particles are nano-sized. 6. The method of claim 1 , wherein the plurality of support particles further comprise zirconium oxide, lanthanum oxide, yttrium oxide, or a combination thereof. 7. The method of claim 1 , wherein the nano-sized PGM on the plurality of support particles comprise composite nano-particles, wherein the composite nano-particles comprise a support-nano-particle and a PGM nano-particle. 8. The method of claim 7 , wherein the composite nano-particles are bonded to micron-sized carrier particles to form nano-on-nano-on-micro particles. 9. The method of claim 8 , wherein the micron-sized carrier particles comprise cerium oxide, zirconium oxide, lanthanum oxide, yttrium oxide, or a combination thereof. 10. The method of claim 8 , wherein the micron-sized carrier particles comprise 86 wt % cerium oxide, 10 wt % zirconium oxide, and 4 wt % lanthanum oxide. 11. The method of claim 7 , wherein the composite nano-particles are embedded within carrier particles to form nano-on-nano-in-micro particles. 12. The method of claim 7 , wherein the composite nanoparticles are plasma created. 13. The method of claim 1 , wherein the PGM comprises palladium and/or ruthenium. 14. The method of claim 1 , wherein the PNA layer comprises about 2 g/L to about 4 g/L palladium and/or about 3 g/L to about 15 g/L ruthenium. 15. The method of claim 1 , wherein the PNA layer comprises greater than or equal to about 150 g/L of the plurality of support particles. 16. The method of claim 1 , wherein the PNA layer further comprises boehmite particles. 17. The method of claim 16 , wherein the nano-sized PGM on the plurality of support particles comprises 95% to 98% by weight of the mixture of the nano-sized PGM on the plurality of support particles and the boehmite particles in the PNA layer and/or the boehmite particles comprise 2% to 5% by weight of the mixture of the nano-sized PGM on the plurality of support particles and boehmite particles in the PNA layer. 18. The method of claim 1 , wherein the substrate comprises cordierite. 19. The method of claim 1 , wherein the substrate comprises a honeycomb structure. 20. The method of claim 1 , wherein a corner-fill layer is deposited directly on the substrate.

Assignees

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Classifications

  • Coatings comprising a zeolite · CPC title

  • Coatings comprising several layers · CPC title

  • with rare earths or actinides · CPC title

  • Platinum · CPC title

  • Diesel engines and lean burn gasoline engines · CPC title

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What does patent US10086356B2 cover?
The present disclosure relates to a substrate containing passive NOx adsorption (PNA) materials for treatment of gases, and washcoats for use in preparing such a substrate. Also provided are methods of preparation of the PNA materials, as well as methods of preparation of the substrate containing the PNA materials. More specifically, the present disclosure relates to a coated substrate containi…
Who is the assignee on this patent?
Umicore Ag & Co Kg
What technology area does this patent fall under?
Primary CPC classification B01J20/02. Mapped technology areas include Operations & Transport.
When was this patent published?
Publication date Tue Oct 02 2018 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 10 related publications on this page (citations in our corpus or others sharing the same primary CPC).