Method for converting a high-boiling hydrocarbon feedstock into lighter boiling hydrocarbon products
US-2017121613-A1 · May 4, 2017 · US
US11041127B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11041127-B2 |
| Application number | US-201816639215-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 10, 2018 |
| Priority date | Aug 15, 2017 |
| Publication date | Jun 22, 2021 |
| Grant date | Jun 22, 2021 |
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.
Provided are systems and methods for obtaining ethylene and propylene products from, for example, shale gas and shale gas condensate feedstocks. These systems and method operate by utilizing a hydrocracker train to crack C4 and C5 hydrocarbons to a product stream of propane and ethane or using a hydrogenolysis train to process C4 and C5 hydrocarbons to a product stream of propane and ethane that is provided to a cracker for an efficient conversion to ethylene and propylene. The disclosed systems are configured to reduce the amount of offsite hydrogen needed and also provide product streams that include a well-defined set of products as compared to existing approaches.
Opening claim text (preview).
What is claimed: 1. A method of producing alkene products from a feedstock, the method comprising: separating the feedstock, with a first separation train, into a light feedstock fraction comprising C1-C5 alkanes and a heavy feedstock fraction comprising C6+ alkanes; effecting a cyclization process, with a cyclization train, on the heavy feedstock fraction so as to give rise to one or more of least benzene, toluene, xylenes, one or more gasoline range products, and cyclization train hydrogen; removing methane, with a demethanizing train, from the light feedstock fraction so as to give rise to a demethanized light feedstock fraction comprising C2-C5 alkanes; separating, with a second separation train, the demethanized light feedstock fraction so as to separate C2 and C3 alkanes from C4 and C5 alkanes; (i) cracking, with a hydrocracker train, C5 alkanes developed at the second separation train and, optionally C4 alkanes developed at the second separation train, so as to give rise to a hydrocracker product stream comprising C1-C3 alkanes and communicating at least some of the hydrocracker product stream comprising C1-C3 alkanes to the demethanizing train or (ii) processing, with a hydrogenolysis train, C5 alkanes developed at the second separation train and, optionally C4 alkanes developed at the second separation train, so as to give rise to a hydrogenolysis product stream comprising C1-C3 alkanes and communicating at least some of the hydrogenolysis product stream comprising C1-C3 alkanes to the demethanizing train; and cracking, with an alkane cracker train, C2 and C3 alkanes separated at the second separation train so as to give rise to an alkene product stream comprising C2 and C3 alkenes; and cracking, with an alkane cracker train, C2 and C3 alkanes separated at the second separation train so as to give rise to an alkene product stream comprising C2 and C3 alkenes. 2. The method of claim 1 , further comprising communicating at least some of the cyclization train hydrogen to the hydrocracker train. 3. The method of claim 1 , further comprising combusting at least some of the methane removed by the demethanizing train so as to supply heat to one or more of the first separation train, the cyclization train, the demethanizing train, the second separation train, and the alkane cracker train. 4. The method of claim 3 , wherein combusting the methane provides within about 10% of the heat utilized by one or more of the first separation train, the cyclization train, the demethanizing train, the second separation train, and the alkane cracker train. 5. The method of claim 1 , wherein the alkane cracker train is characterized as a gas cracker. 6. The method of claim 1 , further comprising communicating, to the hydrocracker train or to the hydrogenolysis train, whichever present, at least some of the gasoline range products from the cyclization train, and further comprising cracking or effecting hydrogenolysis on the gasoline range products to form methane and C2-C3 alkanes. 7. The method of claim 1 , further comprising effecting dehydrogenation and metathesis on C4 alkanes developed at the second separation train so as to give rise to one or both of C2 and C3 alkenes. 8. The method of claim 7 , further comprising communicating hydrogen evolved in the dehydrogenation, metathesis, or both, to the hydrocracker train or the hydrogenolysis train, whichever present. 9. The method of claim 7 , further comprising communicating, to the cyclization train, hexene evolved by the metathesis.
including at least one step of thermal cracking in the absence of hydrogen · CPC title
the catalyst containing platinum group metals or compounds thereof · CPC title
plural parallel stages only · CPC title
Aromatisation of hydrocarbon oil fractions · CPC title
C2-C4 olefins · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.