Catalyst for producing gamma-valerolactone, method for preparing the same and method for manufacturing gamma-valerolactone using the same
US-2019134616-A1 · May 9, 2019 · US
US10953396B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10953396-B2 |
| Application number | US-201916502601-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 3, 2019 |
| Priority date | Jul 3, 2019 |
| Publication date | Mar 23, 2021 |
| Grant date | Mar 23, 2021 |
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A method of making a multifunctional catalyst for upgrading pyrolysis oil includes contacting a hierarchical mesoporous zeolite support with a solution including at least a first metal catalyst precursor and a second metal catalyst precursor, each or both of which may include a heteropolyacid. The hierarchical mesoporous zeolite support may have an average pore size of from 2 nm to 40 nm. Contacting the hierarchical mesoporous zeolite support with the solution deposits or adsorbs the first metal catalyst precursor and the second catalyst precursor onto outer surfaces and pore surfaces of the hierarchical mesoporous zeolite support to produce a multifunctional catalyst precursor. The method further includes removing excess solution and calcining the multifunctional catalyst precursor to produce the multifunctional catalyst comprising at least a first metal catalyst and a second metal catalyst deposited on the outer surfaces and pore surfaces of the hierarchical mesoporous zeolite support.
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What is claimed is: 1. A method of making a multifunctional catalyst for upgrading pyrolysis oil, the method comprising: contacting a hierarchical mesoporous zeolite support with a solution comprising at least a first metal catalyst precursor and a second metal catalyst precursor, where: the hierarchical mesoporous zeolite support has an average pore size of from 2 nanometers to 40 nanometers as determined by Barrett-Joyner-Halenda (BJH) analysis; the first metal catalyst precursor, the second metal catalyst precursor, or both, comprises a heteropolyacid having at least one heteroatom selected from the group consisting of phosphorous, silicon, germanium, arsenic, and combinations of these; and the contacting deposits the first metal catalyst precursor and the second metal catalyst precursor onto outer surfaces and pore surfaces of the hierarchical mesoporous zeolite support to produce a multifunctional catalyst precursor; removing excess solution from the multifunctional catalyst precursor; and calcining the multifunctional catalyst precursor to produce the multifunctional catalyst comprising at least a first metal catalyst and a second metal catalyst deposited on the outer surfaces and pore surfaces of the hierarchical mesoporous zeolite support. 2. The method of claim 1 , in which the hierarchical mesoporous zeolite support comprises a hierarchical mesoporous beta zeolite support. 3. The method of claim 1 , in which the hierarchical mesoporous zeolite support has an average pore size of from 5 nanometers to 25 nanometers as determined by BJH analysis. 4. The method of claim 1 , in which the hierarchical mesoporous zeolite support has a total pore volume of greater than or equal to 0.35 cubic centimeters per gram. 5. The method of claim 1 , in which the hierarchical mesoporous zeolite support comprises a molar ratio of silica to alumina of from 20 to 100. 6. The method of claim 1 , further comprising producing the hierarchical mesoporous zeolite support. 7. The method of claim 6 , in which producing the hierarchical mesoporous zeolite support comprises converting a microporous parent zeolite into the hierarchical mesoporous zeolite support through desilication of the microporous parent zeolite. 8. The method of claim 7 , in which desilication of the microporous parent zeolite to produce the hierarchical mesoporous zeolite support comprises: mixing the microporous zeolite with an aqueous metal hydroxide solution; and heating the microporous zeolite and aqueous metal hydroxide mixture to a temperature of greater than or equal to 100 degrees Celsius to produce the hierarchical mesoporous zeolite support. 9. The method of claim 1 , in which the heteropolyacid comprises: at least one metal selected from cobalt, molybdenum, vanadium, or combinations of these. 10. The method of claim 1 , in which the first metal catalyst precursor comprises the heteropolyacid. 11. The method of claim 1 , in which the first metal catalyst precursor comprises a first heteropolyacid and the second metal catalyst precursor comprises a second heteropolyacid that is different from the first heteropolyacid. 12. The method of claim 11 , in which the first heteropolyacid or the second heteropolyacid is H 3 PMo 12 O 40 . 13. The method of claim 1 , in which the heteropolyacid comprises phosphormolybdic hetereopolyacid having formula H 3 PMo 12 O 40 . 14. The method of claim 1 , in which removing the excess solution from the multifunctional catalyst precursor comprises filtering or decanting the excess solution from the multifunctional catalyst precursor and drying the multifunctional catalyst precursor to remove solvent. 15. The method of claim 1 , in which the first metal catalyst comprises molybdenum and the second metal catalyst comprises cobalt, where at least the heteropolyacid includes the molybdenum. 16. The method of claim 1 , in which the multifunctional catalyst comprises phosphorous deposited on the outer surfaces and pore surfaces of the hierarchical mesoporous zeolite support. 17. The method of claim 1 , in which the hierarchical mesoporous zeolite support comprises an acidity of less than 15,000 micromoles of ammonia per gram.
Aromatics · CPC title
Catalyst aspects · CPC title
Pressure · CPC title
Temperature · CPC title
Aromatics or polyaromatics · CPC title
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