Preparation of propane oxidation catalysts
US-9517451-B2 · Dec 13, 2016 · US
US10589258B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10589258-B2 |
| Application number | US-201715651366-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 17, 2017 |
| Priority date | Jul 19, 2016 |
| Publication date | Mar 17, 2020 |
| Grant date | Mar 17, 2020 |
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The preparation of an oxidative dehydrogenation catalyst comprising Mo, V, Nb and Te using a hydrothermal step the activity and reproducibility of the catalyst is improved by conduction the hydrothermal step at higher pressures while permitting gaseous products to leave the reactor. In some instances a condenser may be upstream of the pressure relief valve.
Opening claim text (preview).
What is claimed is: 1. A process for synthesis of a catalyst for oxidative dehydrogenation of paraffins via a hydrothermal treatment comprising: i) preparing an aqueous slurry comprising Mo, V, Nb and Te salts in a molar ratio of metal elements 1:0.3 to 3; 0.05 to 0.25; and 0.08 to 0.2 at a temperature from 25° C. to 80° C.; ii) heating the slurry in a reactor to a temperature from 80° to 220° C. at a pressure equal or above the saturated water vapor pressure at the corresponding reaction temperature, for a period of time not less than 1 hour with agitation and simultaneous removal of gaseous byproduct species produced during the reaction; iii) letting the reactor cool and depressurizing the reactor and recovering the catalyst as a solid. 2. The process according to claim 1 , wherein the temperature of the reactor is from 150° C.-185° C. 3. The process according to claim 2 , wherein the pressure in the reactor is from 10 psi to 190 psi (960 kPa to 1300 kPa). 4. The process according to claim 1 , wherein there is a condenser upstream of a pressure control device. 5. The process according to 4, wherein the condenser is operated at a temperature above 0° C. and below reaction temperature. 6. The process according to claim 1 , wherein the gaseous byproduct species are removed by being vented from the reactor through a pressure control device. 7. The process according to claim 1 , wherein the gaseous byproduct species are removed from the reactor using one or more methods selected from gas absorption, gas adsorption, membrane separation, and chemicals transformation. 8. The process according to claim 1 wherein the time of hydrothermal treatment is from 1 to 72 hours. 9. The process according to claim 8 , wherein the reactor is metal. 10. The process according to claim 9 , wherein the reactor can be lined or the reactor contains glass fibers, beads, or other nucleating agents. 11. The process according to claim 10 , wherein the reactor is lined and the lining comprises one or more of ceramic based material, a different metal, fluorocarbon polymers and combinations thereof. 12. The process according to claim 11 , wherein the aqueous slurry comprises a molar ratio Mo, V, Nb and Te salts 1: 0.5 to 1.0: 0.08 to 0.20: 0.10 to 0.20. 13. The process according to claim 12 , wherein step iii) further includes separating a resulting precatalyst from the aqueous phase and washing it with distilled water or an aqueous oxalate solution and drying the precatalyst to form the catalyst. 14. The process according to claim 13 , further comprising grinding the catalyst. 15. The process according to claim 14 , further including step iv) calcining the catalyst in an inert atmosphere at a temperature from 200° C. to 650° C. for a time from 1 to 20 hours. 16. The process according to claim 15 wherein the calcined catalyst comprises the following molar ratios: Mo1:V 0.32-0.49:Te 0.10-0.17:Nb 0.14-0.17 as determine by PIXE.
Precipitation · CPC title
Vanadium · CPC title
Grinding · CPC title
Vanadium, niobium or tantalum · CPC title
in the presence of water, e.g. steam · CPC title
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