Process and system for conversion of crude oil to chemicals and fuel products integrating steam cracking and fluid catalytic cracking
US-2018142167-A1 · May 24, 2018 · US
US11242299B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11242299-B2 |
| Application number | US-201816156634-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 10, 2018 |
| Priority date | Oct 10, 2018 |
| Publication date | Feb 8, 2022 |
| Grant date | Feb 8, 2022 |
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Embodiments of methods of synthesizing a metathesis catalyst system, which include impregnating tungsten oxide on silica support in the presence of a precursor to produce a base catalyst; calcining the base catalyst; impregnating a metal oxide co-catalyst comprising a metal oxide onto the surface of the base catalyst to produce a doped catalyst; and calcining the doped catalyst to produce a metathesis catalyst system. Further embodiments of processes for the production of propylene, which include contacting a hydrocarbon feedstock comprising a mixture of 1-butene and 2-butene with embodiments of the metathesis catalyst system to produce, via metathesis conversion, a product stream comprising propylene.
Opening claim text (preview).
What is claimed is: 1. A method of synthesizing a metathesis catalyst system comprising: impregnating a metal oxide onto a large pore silica support in a presence of a precursor to produce a base catalyst comprising a metal oxide; calcining the base catalyst at a first temperature for a first time period and a second temperature for a second time period; impregnating from about 0.5 wt. % to about 2.5 wt. % of a metal oxide co-catalyst, based on a total weight of the metathesis catalyst system, onto the base catalyst to produce a doped catalyst, wherein the metal oxide co-catalyst comprises Ce, Ni, or both Ce and Ni; and calcining the doped catalyst at a third temperature for a third time period and a fourth temperature for a fourth time period to produce the metathesis catalyst system. 2. The method of claim 1 , wherein the large pore silica support comprises an amorphous silica. 3. The method of claim 1 , wherein the base catalyst comprises from about 8 wt. % to about 12 wt. % tungsten oxide, based on a total weight of the base catalyst. 4. The method of claim 1 , wherein the precursor comprises ammonium metatungstate hexahydrate. 5. The method of claim 1 , wherein the metathesis catalyst system has one or more of a surface area of about 400 m 2 /g to about 800 m 2 /g, a pore size distribution of about 3 nm to about 40 nm, and a total pore volume of at least 0.700 cm 3 /g to about 2.5 cm 3 /g. 6. The method of claim 1 , wherein the metal oxide co-catalyst comprises Ce. 7. The method of claim 1 , wherein the metal oxide co-catalyst comprises Ni. 8. The method of claim 1 , wherein the first temperature and the third temperature are 250° C. 9. The method of claim 1 , wherein the second temperature and the fourth temperature are 550° C. 10. The method of claim 1 , wherein the first time period and the third time period are 2 hours. 11. The method of claim 1 , wherein the second time period and the fourth time period are 8 hours. 12. A method of synthesizing a metathesis catalyst system comprising: impregnating a metal oxide onto a large pore silica support in a presence of a precursor to produce a base catalyst comprising the metal oxide, wherein the large pore silica support comprises an amorphous silica; calcining the base catalyst at a first temperature for a first time period and a second temperature for a second time period; impregnating from about 0.5 wt. % to about 2.5 wt. % of a metal oxide co-catalyst, based on a total weight of the metathesis catalyst system, onto the base catalyst to produce a doped catalyst, wherein the metal oxide co-catalyst comprises Ce, Ni, or both Ce and Ni; and calcining the doped catalyst at a third temperature for a third time period and a fourth temperature for a fourth time period to produce the metathesis catalyst system; and wherein the metathesis catalyst system has one or more of a surface area of about 400 m 2 /g to about 800 m 2 /g, a pore size distribution of about 3 nm to about 40 nm, and a total pore volume of at least 0.700 cm 3 /g to about 2.5 cm 3 /g. 13. The method of claim 12 , wherein the base catalyst comprises from about 8 wt. % to about 12 wt. % tungsten oxide, based on a total weight of the base catalyst. 14. The method of claim 12 , wherein the precursor comprises ammonium metatungstate hexahydrate. 15. The method of claim 12 , wherein the metal oxide co-catalyst comprises Ce. 16. The method of claim 12 , wherein the metal oxide co-catalyst comprises Ni.
X-ray diffraction · CPC title
characterised by their amorphous structures · CPC title
characterised by their crystalline properties, e.g. semi-crystalline (catalysts comprising carbon B01J21/18; molecular sieves B01J29/00) · CPC title
in several steps · CPC title
Propene · CPC title
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