Heterogeneous catalysts for the oxidative dehydrogenation of alkanes or oxidative coupling of methane
US-2017066700-A1 · Mar 9, 2017 · US
US10501322B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10501322-B2 |
| Application number | US-201715843305-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 15, 2017 |
| Priority date | Dec 19, 2016 |
| Publication date | Dec 10, 2019 |
| Grant date | Dec 10, 2019 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Improved methods of synthesizing oxygen-functionalized boron nitride (O—BN) are disclosed. In the disclosed methods, boron nitride (BN) in any form is contacted with a gaseous composition or compositions that include oxygen and an organic compound, such as, but not limited to, a hydrocarbon.
Opening claim text (preview).
We claim: 1. A method of making oxygen-functionalized boron nitride (O—BN), comprising contacting boron nitride (BN) simultaneously with one or more compositions that together comprise both oxygen and one or more organic compounds, whereby the boron nitride becomes oxygen-functionalized boron nitride (O—BN). 2. The method of claim 1 , wherein the one or more compositions are gaseous. 3. The method of claim 2 , wherein the boron nitride is contacted with the one or more gaseous compositions by a continuous flow of the one or more gaseous compositions over the surface of the boron nitride. 4. The method of claim 2 , wherein the one or more gaseous compositions further comprise nitrogen. 5. The method of claim 1 , wherein the boron nitride is in the form of hexagonal boron nitride (h-BN), boron nitride nanomeshes (h-BN nanomeshes), boron nitride nanosheets (BNNSs), boron nitride nanoribbons (BNNRs) or boron nitride nanotubes (BNNTs). 6. The method of claim 1 , wherein the one or more organic compounds include 3 or more carbon atoms (are C 3+ organic compounds), 4 or more carbon atoms (are C 4+ organic compounds), 5 or more carbon atoms (are C 5+ organic compounds), 6 or more carbon atoms (are C 6+ organic compounds), 7 or more carbon atoms (are C 7+ organic compounds), or 8 or more carbon atoms (are C 8+ organic compounds). 7. The method of claim 1 , wherein the one or more organic compounds are selected from the group consisting of aliphatic hydrocarbons, an aromatic hydrocarbons, alcohols, ketones, aldehydes, carboxylic acids, carbonates, a boronic acids, and borinic acids. 8. The method of claim 1 , wherein the one or more organic compounds have from one to ten carbon atoms. 9. The method of claim 8 , wherein the one or more organic compounds have from four to ten carbon atoms. 10. The method of claim 8 , wherein the organic compound is selected from the group consisting of methane, ethane, propane, isobutane, and n-butane. 11. The method of claim 1 , wherein the one or more organic compounds are not propane. 12. The method of claim 1 , wherein the boron nitride is contacted with the one or more compositions for a total of 2-200 hours. 13. The method of claim 1 , wherein the boron nitride is contacted with the one or more compositions at a temperature of 200° C.-900° C. 14. The method of claim 13 , wherein the boron nitride is contacted with the one or more compositions at a temperature of 200° C.-500° C. 15. The method of claim 13 , wherein the boron nitride is contacted with the one or more compositions at a temperature of less than 500° C. 16. The method of claim 13 , wherein the boron nitride is contacted with the one or more compositions at a temperature of 250° C.-850° C. 17. The method of claim 1 , wherein the one or more compositions are gaseous, and wherein the one or more organic compounds in the one or more compositions have a concentration (Mol % organic compound ) of 0.05-0.95 Mol %. 18. The method of claim 1 , wherein the one or more compositions are gaseous, and wherein the oxygen in the one or more compositions has a concentration (Mol % O2 ) of 0.05-0.95 Mol %. 19. The method of claim 1 , wherein the one or more compositions are gaseous, and wherein the boron nitride is contacted with the one or more gaseous compositions by a continuous flow of the one or more gaseous compositions over the surface of the boron nitride, and wherein the total flow rate of the one or more gaseous compositions over the surface of the boron nitride is 10-1000 mL/min. 20. The method of claim 19 , wherein the total flow rate of the one or more gaseous compositions over the surface of the boron nitride is 60 mL/min or higher. 21. The method of claim 1 , further comprising the step of removing water from the O—BN surface or from the environment adjacent to the O—BN surface.
After-treatment, e.g. grinding, purification (transformation of hexagonal into cubic or wurtzitic boron nitride C04B35/5831) · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.