System and process for steam cracking and pfo treatment integrating selective hydrogenation, ring opening and naphtha reforming
US-2021130716-A1 · May 6, 2021 · US
US12017990B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12017990-B2 |
| Application number | US-202217965614-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 13, 2022 |
| Priority date | Oct 14, 2021 |
| Publication date | Jun 25, 2024 |
| Grant date | Jun 25, 2024 |
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.
The present disclosure provides systems and methods for producing aromatic compounds in high yield from a mixed aromatic feed stream. Also disclosed are systems and methods for producing aromatic compounds in high yield from oxygenated hydrocarbons such as carbohydrates, sugars, sugar alcohols, sugar degradation products, and the like.
Opening claim text (preview).
The invention claimed is: 1. A method for producing and separating a xylene isomer, the method comprising: (i) contacting a mixed aromatic feed stream comprising C 7+ aromatics with an aromatics processing catalyst to produce a product stream comprising an increased concentration of C 8 aromatics relative to the mixed aromatic feed stream, wherein the aromatics processing catalyst comprises a transalkylation catalyst, a dealkylation catalyst, a hydrocracking catalyst or a combination thereof; (ii) fractionating, using a distillation column, the product stream into a C 7− stream and a C 8+ stream; (iii) fractionating, using a distillation column, at least a portion of the C 8+ stream into a C 8 stream and a C 9+ stream; (iv) subjecting at least a portion of the C 8 stream to an isomer-recovery process unit to produce a xylene isomer stream and a raffinate stream comprising non-recovered C 8 compounds; and (v) contacting the raffinate stream with an isomerization catalyst to produce an isomerization product stream, wherein the isomerization product stream comprises at least one xylene isomer, wherein at least a portion of the isomerization product stream is combined with the C 8 stream prior to entering the isomer-recovery process unit, and wherein at least a portion of the C 8+ stream bypasses the distillation column in step (iii) and is combined with the C 8 stream prior to entering the isomer-recovery process unit. 2. The method of claim 1 , wherein the xylene isomer stream comprises para-xylene, ortho-xylene, or meta-xylene. 3. The method of claim 1 , wherein prior to step (i) the method comprises: contacting an aqueous hydrocarbon feedstock comprising water and one or more oxygenate with a condensation catalyst to produce a condensation product stream comprising C4+ compounds, wherein the C4+ compounds comprise a C 4+ alcohol, a C 4+ ketone, a C 4+ alkane, a C 4+ alkene, a C 5+ cycloalkane, a C 5+ cycloalkene, an aryl, or a fused aryl; fractionating the condensation product stream to separate a C 6− stream from a C 7+ stream; recycling the C 6− stream to the condensation catalyst; fractionating the C 7+ stream into a C 7-10 stream and a C 11+ stream, wherein the C 7-10 stream forms the mixed aromatic feed stream. 4. The method of claim 1 , wherein, based on the total weight of the mixed aromatic feed stream, the mixed aromatic feed stream comprises: from 0.1 wt % to 45 wt % olefins; from 0.1 wt % to 25 wt % naphthenes; from 0.1 wt % to 40 wt % naphtheno-olefins; phenols in an amount from 10 ppm to 10 wt %; and/or oxygenates in an amount from 10 ppm to 10 wt %. 5. The method of claim 1 , wherein the mixed aromatic feed stream has a bromine number of at least 1 mg Br 2 /g of the mixed aromatic feed to less than 100 mg Br 2 /g of the mixed aromatic feed. 6. The method of claim 1 , wherein the mixed aromatic feed stream comprises C 9-10 aromatics. 7. The method of claim 5 , wherein the C 7− stream is fed to a distillation column that fractionates the C 7− stream into a C 6− stream and a C 7 stream. 8. The method of claim 7 , wherein at least a portion of the C 7 stream is recycled and combined with the mixed aromatic feed stream. 9. The method of claim 1 , wherein the C 9+ stream is fed to a fourth distillation column that fractionates the C 9+ stream into a C 9-10 stream and a C 11+ stream, wherein the C 9-10 stream is recycled and combined with the mixed aromatic feed stream. 10. The method of claim 1 , wherein at least a portion of the isomerization product stream is combined with the product stream produced from the aromatics processing catalyst in step (i). 11. The method of claim 10 , wherein the method further comprises: fractionating the C 7− stream into a C 6− stream and a C 7 stream; and fractionating the C 9+ stream into a C 9-10 stream and a C 11+ stream, wherein the C 7 stream and the C 9-10 stream are recycled and combined with the mixed aromatic feed stream. 12. The method of claim 10 , wherein the method further comprises: fractionating the C 7− stream into a C 6− stream and a C 7 stream; and fractionating the C 9+ stream into a C 9-10 stream and a C 11+ stream, wherein the C 7 stream is recycled and combined with the mixed aromatic feed stream and the C 9+ stream is recovered as a product. 13. The method of claim 1 , wherein the isomer-recovery process unit comprises an adsorption unit or a crystallization unit. 14. The method of claim 1 , wherein the aromatics processing catalyst comprises an acid catalyst, which comprises aluminosilicates, tungstated aluminosilicates, silica-alumina phosphates, aluminum phosphates, amorphous silica alumina, zirconia, sulfated zirconia, tungstated zirconia, tungsten carbide, molybdenum carbide, titania, acidic alumina, phosphated alumina, tungstated alumina, phosphated silica, tungstated silica, tungstated titania, tungstated phosphate, niobia, sulfated carbons, phosphated carbons, acidic resins, heteropolyacids, tungstated heteropolyacid, inorganic acids, or a combination thereof; and wherein the acid catalyst comprises a metal, which comprises Cu, Ag, Au, Pt, Ni, Fe, Co, Ru, Rh, Zn, Ga, In, Pd, Ir, Re, Mn, Cr, Mo, W, Sn, Os, alloys, or a combination thereof. 15. The method of claim 1 , wherein step (i) occurs at a temperature from 200° C. to 600° C., a pressure from 100 psig to 1500 psig, or a weight hourly space velocity (WHSV) from 0.1 to 10 mass feed/mass catalyst/hour, or wherein step (i) comprises feeding hydrogen in an amount of at least 0.1 mol of hydrogen per mol of mixed aromatic feed.
Aromatics · CPC title
Aromatics or polyaromatics · CPC title
by adsorption, i.e. purification or separation of hydrocarbons with the aid of solids, e.g. with ion-exchangers · CPC title
with the aid of auxiliary compounds · CPC title
Processes comprising at least two steps in series · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.