Rate/kinetic selective multiple bed adsorption process cycle
US-11883775-B2 · Jan 30, 2024 · US
US9446381B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9446381-B2 |
| Application number | US-201214235124-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 27, 2012 |
| Priority date | Jul 28, 2011 |
| Publication date | Sep 20, 2016 |
| Grant date | Sep 20, 2016 |
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This disclosures provides an adsorbent which, on the basis of the total weight of the adsorbent, comprises: 1) a Si—Al molecular sieve having an A-FAU structure, wherein A represents a monovalent cation, in an amount of 1-20 wt %, 2) at least one binder selected from the group consisting of titanium dioxide, stannic oxide, zirconium oxide and alumina, in an amount of 3-35 wt %, 3) a silica source, in an amount of 5-40 wt %, 4) zinc oxide, in an amount of 10-80 wt %, and 5) at least one promoter metal selected from the group consisting of cobalt, nickel, iron and manganese, based on the metal, in an amount of 5-30 wt %, wherein at least 10 wt % of the promoter metal is present in a reduced valence state. This adsorbent exhibits improved activity and stability, and at the same time, is capable of significantly improving the octane number of the product gasoline.
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The invention claimed is: 1. A desulfurization adsorbent for hydrocarbon oil, on the basis of the total weight of the adsorbent, comprising: 1) a Si—Al molecular sieve having an A-FAU structure, wherein A represents a monovalent cation, in an amount of 1-20 wt %, 2) at least one binder selected from the group consisting of titanium dioxide, stannic oxide, zirconium oxide and alumina, in an amount of 3-35 wt %, 3) a silica source, in an amount of 5-40 wt %, 4) zinc oxide, in an amount of 10-80 wt %, and 5) at least one promoter metal selected from the group consisting of cobalt, nickel, iron and manganese, based on the metal, in an amount of 5-30 wt %, wherein at least 10 wt % of the promoter metal is present in a reduced valence state, wherein the absorbent contains no rare earth compound. 2. The adsorbent according to claim 1 , wherein the Si—Al molecular sieve having an A-FAU structure is in an amount of 2-15 wt %, the binder is in an amount of 5-25 wt %, the silica source is in an amount of 10-30 wt %, the zinc oxide is in an amount of 25-70 wt %, and the promoter metal is in an amount of 8-25 wt %. 3. The adsorbent according to claim 1 , wherein the Si—Al molecular sieve having an A-FAU structure is in an amount of 2-10 wt %, the binder is in an amount of 8-15 wt %, the silica source is in an amount of 12-25 wt %, the zinc oxide is in an amount of 40-60 wt %, and the promoter metal is in an amount of 12-20 wt %. 4. The adsorbent according to claim 1 , wherein the silica source is silica or a natural mineral having a silica content of more than 45 wt %. 5. The adsorbent according to claim 1 , wherein the Si—Al molecular sieve having an A-FAU structure is a X-molecular sieve, a Y-molecular sieve, or a mixture thereof. 6. A process for producing the desulfurization adsorbent for hydrocarbon oil according to claim 1 , comprising: (1) contacting at least one binder with a silica source, a Si—Al molecular sieve having an A-FAU structure (wherein A represents a monovalent cation), and zinc oxide to obtain a carrier, wherein the binder is titanium dioxide, stannic oxide, zirconium oxide, or alumina; (2) contacting the carrier with a promoter metal-containing compound to obtain an adsorbent precursor; and (3) under a condition sufficient to present at least 10 wt % of the promoter metal in a reduced valence state, treating the adsorbent precursor to obtain the desulfurization adsorbent for hydrocarbon oil. 7. The process according to claim 6 , wherein the step (1) further comprises: (1a) mixing the binder or a binder precursor with an acid to form a slurry, and (1b) mixing the slurry, the silica source, the Si—Al molecular sieve having an A-FAU structure and zinc oxide, and molding, drying, and calcining the mixture to obtain the carrier. 8. The process according to claim 7 , wherein the binder precursor is at least one selected from the group consisting of halides, alkoxylates, carboxylic acid salts, hydrated oxides, hydroxides, hydrated hydroxides and oxyhalides, of titanium, tin, zirconium, or aluminum. 9. The process according to claim 7 , wherein the acid is a water soluble inorganic acid, a water soluble organic acid, or a mixture thereof, and the amount of the acid used is such that the pH value of the slurry reaches 0.5-6. 10. The process according to claim 6 , wherein the step (1) further comprises: (1a′) mixing the silica source and the binder or a binder precursor are mixed with an acid to form a slurry, and (1b′) mixing the slurry, the Si—Al molecular sieve having an A-FAU structure and zinc oxide, and molding, drying, and calcining the mixture to obtain the carrier. 11. The process according to claim 10 , wherein the binder precursor is at least one selected from the group consisting of halides, alkoxylates, carboxylic acid salts, hydrated oxides, hydroxides, hydrated hydroxides, and oxyhalides of titanium, tin, zirconium, or aluminum. 12. The process according to claim 10 , wherein the acid is a water soluble inorganic acid, a water soluble organic acid, or a mixture thereof, and the amount of the acid used is such that the pH value of the slurry reaches 0.5-6. 13. The process according to claim 6 , wherein the step (1) further comprises: (1a′) mixing a part of the silica source and the binder or a binder precursor with an acid to form a slurry, and (1b′) mixing the slurry, the remainder of the silica source, the Si—Al molecular sieve having an A-FAU structure and zinc oxide, and molding, drying, and calcining the mixture to obtain the carrier. 14. The process according to claim 13 , wherein the binder precursor is at least one selected from the group consisting of halides, alkoxylates, carboxylic acid salts, hydrated oxides, hydroxides, hydrated hydroxides, and oxyhalides of titanium, tin, zirconium, or aluminum. 15. The process according to claim 13 , wherein the acid is at least one selected from the group consisting of a water soluble inorganic acid, a water soluble organic acid, or a mixture thereof, and the amount of the acid used is such that the pH value of the slurry reaches 0.5-6. 16. A hydrocarbon oil desulfurization process, comprising: obtaining the desulfurization adsorbing agent for hydrocarbon oil according to claim 1 ; and contacting a sulfur-containing hydrocarbon oil with the desulfurization adsorbent under a condition sufficient to remove at least a part of sulfur from the sulfur-containing hydrocarbon oil. 17. The hydrocarbon oil desulfurization process according to claim 16 , wherein the Si—Al molecular sieve having an A-FAU structure is in an amount of 2-15 wt %, the binder is in an amount of 5-25 wt %, the silica source is in an amount of 10-30 wt %, the zinc oxide is in an amount of 25-70 wt %, and the promoter metal is in an amount of 8-25 wt %. 18. The hydrocarbon oil desulfurization process according to claim 16 , wherein the Si—Al molecular sieve having an A-FAU structure is in an amount of 2-10 wt %, the binder is in an amount of 8-15 wt %, the silica source is in an amount of 12-25 wt %, the zinc oxide is in an amount of 40-60 wt %, and the promoter metal is in an amount of 12-20 wt %. 19. The hydrocarbon oil desulfurization process according to claim 16 , wherein the silica source is silica or a natural mineral having a silica content of more than 45 wt %. 20. The hydrocarbon oil desulfurization process according to claim 16 , wherein the Si—Al molecular sieve having an A-FAU structure is a X-molecular sieve, a Y-molecular sieve, or a mixture thereof.
Iron group metals or copper · CPC title
comprising oxides or hydroxides of metals not provided for in group B01J20/04 · CPC title
Removal of non-hydrocarbon compounds, e.g. sulfur compounds · CPC title
Inorganic carriers, supports or substrates · CPC title
Compounds of Fe, Ru, Os, Co, Rh, Ir, Ni, Pd, Pt · CPC title
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