Catalyst for direct NOx decomposition and a method of forming and using the catalyst

US9868111B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9868111-B2
Application numberUS-201615055555-A
CountryUS
Kind codeB2
Filing dateFeb 27, 2016
Priority dateFeb 27, 2016
Publication dateJan 16, 2018
Grant dateJan 16, 2018

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

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A process of forming a direct NOx catalyst includes the steps of providing a palladium salt, providing a silicon oxide support material, mixing the palladium salt and silicon oxide support material in an aqueous solution, evaporating the aqueous solution forming a solid, calcining the solid, and then exposing the calcined solid to a pretreatment gas at a specified temperature to form a desired direct NOx catalyst. When the process includes exposing the calcined solid to helium gas at a temperature of from 650 to 1000° C. the catalyst may include a mixture of palladium and palladium oxide having a particle size of from 5 to 150 nm where the palladium particles are discrete particles without sintering and the mixture may include 41% by weight palladium oxide and 51% by weight palladium metal.

First claim

Opening claim text (preview).

What is claimed is: 1. A process of forming a direct NOx catalyst comprising the steps of: providing a palladium salt; providing a silicon oxide support material; mixing the palladium salt and silicon oxide support material in an aqueous solution; evaporating the aqueous solution forming a solid; calcining the solid; treating the calcined solid to helium gas at a temperature of from 650-1000° C. forming the direct NOx catalyst. 2. The process of claim 1 wherein the palladium salt is selected from the group consisting of: nitrates, chlorides and acetates. 3. The process of claim 1 wherein the step of calcining includes exposing the solid to a temperature of from 450° C. to 650° C. for a time period of from 3 to 10 hours. 4. The process of claim 1 wherein the formed direct NOx catalyst includes a mixture of palladium and palladium oxide having a particle size of from 5-150 nm wherein the palladium particles are discrete particles without sintering. 5. The process of claim 1 wherein the formed direct NOx catalyst includes 41% by weight palladium oxide and 51% by weight palladium metal. 6. The process of claim 1 wherein the formed direct NOx catalyst has a NOx conversion of from 20 to 40% at a temperature of from 300 to 500° C. 7. The process of claim 1 wherein the formed direct NOx catalyst has a NOx conversion of from 0 to 25% at a temperature of from 650 to 800° C. 8. A process of forming a direct NOx catalyst comprising the steps of: providing a palladium salt; providing a silicon oxide support material; mixing the palladium salt and silicon oxide support material in an aqueous solution; evaporating the aqueous solution forming a solid; calcining the solid; treating the calcined solid to hydrogen gas at a temperature of from 300-1000° C. forming the direct NOx catalyst. 9. The process of claim 8 wherein the palladium salt is selected from the group consisting of: nitrates, chlorides and acetates. 10. The process of claim 8 wherein the step of calcining includes exposing the solid to a temperature of from 450° C. to 650° C. for a time period of from 3 to 10 hours. 11. The process of claim 8 wherein the formed direct NOx catalyst includes palladium particles having a particle size of from 50-2000 nm. 12. The process of claim 8 wherein the formed direct NOx catalyst has a NOx conversion of from 10 to 50% at a temperature of from 300 to 800° C. 13. A process of forming a direct NOx catalyst comprising the steps of: providing a palladium salt; providing a silicon oxide support material; mixing the palladium salt and silicon oxide support material in an aqueous solution; evaporating the aqueous solution forming a solid; calcining the solid; treating the calcined solid to oxygen gas at a temperature of from 50-650° C. forming the direct NOx catalyst. 14. The process of claim 13 wherein the palladium salt is selected from the group consisting of: nitrates, chlorides and acetates. 15. The process of claim 13 wherein the step of calcining includes exposing the solid to a temperature of from 450° C. to 650° C. for a time period of from 3 to 10 hours.

Assignees

Inventors

Classifications

  • Nanoparticles · CPC title

  • Scanning electron microscopy; Transmission electron microscopy · CPC title

  • Indexing scheme associated with group B01J35/00, related to the analysis techniques used to determine the catalysts form or properties · CPC title

  • X-ray diffraction · CPC title

  • Precipitation on carriers · CPC title

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What does patent US9868111B2 cover?
A process of forming a direct NOx catalyst includes the steps of providing a palladium salt, providing a silicon oxide support material, mixing the palladium salt and silicon oxide support material in an aqueous solution, evaporating the aqueous solution forming a solid, calcining the solid, and then exposing the calcined solid to a pretreatment gas at a specified temperature to form a desired …
Who is the assignee on this patent?
Toyota Eng & Mfg North America
What technology area does this patent fall under?
Primary CPC classification B01J23/44. Mapped technology areas include Operations & Transport.
When was this patent published?
Publication date Tue Jan 16 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 2 related publications on this page (citations in our corpus or others sharing the same primary CPC).