Methods and systems for producing light olefins from naphtha
US-2020399546-A1 · Dec 24, 2020 · US
US12545845B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12545845-B2 |
| Application number | US-202318506264-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 10, 2023 |
| Priority date | Dec 8, 2022 |
| Publication date | Feb 10, 2026 |
| Grant date | Feb 10, 2026 |
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.
Processes for rapidly and accurately predicting the fouling potential of a heavy petroleum fraction in a commercial refinery, informing the selection of one or more interventions to prevent or decrease the rate of said fouling. The process utilizes several specialized 13 C Nuclear Magnetic Resonance procedures to more accurately quantify tertiary and quaternary bridgehead aromatic carbon in the heavy petroleum fraction This permits more accurate calculation of a Condensation Index for the heavy petroleum fraction to more accurately predict fouling potential of the fraction. When the condensation index is at or above a threshold value, the process implements one or more responses to improve operational efficiency of the commercial refinery.
Opening claim text (preview).
We claim: 1 . A process for decreasing fouling caused during upgrading of a feed stream comprising a heavy petroleum fraction in a refinery, comprising the steps of: a. providing a sample of a feed stream comprising a heavy petroleum fraction with a boiling point range that is in the range from 343° C. to 566° C.: b. analyzing the sample to calculate an aromatic condensation index value, wherein the aromatic condensation index is determined by: i. performing conventional 13 C nuclear magnetic resonance spectroscopy with inverse gated 1 H decoupling on a portion of the sample to produce a first spectrum comprising resonance peaks indicative of total aromatic content; ii. performing distortionless enhancement by polarization transfer 13 C nuclear magnetic resonance spectroscopy on a portion of the sample utilizing a selection angle of 135 degrees to produce a second spectrum comprising resonance peaks indicative of tertiary aromatic carbon content; iii. performing a quaternary-only 13 C nuclear magnetic resonance spectroscopy on a portion of the sample to produce a third spectrum comprising resonance peaks indicative of quaternary aromatic carbon content; iv. normalizing the sum of the second spectrum and the third spectrum to the first spectrum by fitting the sum of spectral data points for the second and third spectrum at a given chemical shift value to the value for the spectral data point for the first spectrum at the same chemical shift value, then repeating this process for each spectral data point while minimizing the total sum of squared residuals to produce a normalized second spectrum and a normalized third spectrum, wherein the normalization is performed for the chemical shift region of the second spectrum and the third spectrum that is associated with NMR signals for quaternary aromatic carbons and tertiary aromatic carbons; v. integrating the first spectrum, the normalized second spectrum and the normalized third spectrum in the chemical shift range of each spectrum that is associated with NMR signals for aromatic carbons to produce values for total aromatic content, tertiary aromatic carbon content and quaternary aromatic carbon content, respectively; vi. calculating an aromatic condensation index value for the sample by dividing the quaternary aromatic content by the total aromatic content; c. performing at least one of the following actions when the aromatic condensation index value meets or exceeds an aromatic condensation index action threshold value: i. increasing the frequency of periodic cleaning of catalysts, reactors, conduits and heat exchangers contacted by the feed stream during the upgrading; ii. increasing the regeneration frequency for catalysts that contact the feed stream during the upgrading; iii. adding an additive to the feed stream in an amount sufficient to decrease the fouling rate of refinery equipment, comprising catalysts, reactors, conduits and heat exchangers contacted by the feed stream during the upgrading; iv. decreasing at least one reaction temperature to which the feed stream, or any intermediate stream derived therefrom, is exposed during the upgrading; v. altering the flow velocity of the feed stream or any intermediate stream derived therefrom during the upgrading; vi. diluting the feed stream with a second feed stream that has a lower CI, where the diluting occurs at a ratio such that the CI of the resulting mixture is below the CI action threshold value, wherein the second feed stream comprises a second heavy petroleum fraction comprising a boiling point range that is the range from 343° C. to 566° C.; vii. visbreaking the feed stream prior to the upgrading. 2 . The process of claim 1 , wherein the heavy petroleum fraction comprises one or more of heavy gas oil, vacuum gas oil, coker gas oil and cycle oil. 3 . The process of claim 1 , wherein the aromatic condensation index action threshold value is larger than 0.211. 4 . The process of claim 1 , wherein the aromatic condensation index action threshold value is in the range from 0.211 to 0.295. 5 . The process of claim 1 , wherein the conventional 13 C nuclear magnetic resonance spectroscopy with inverse gated 1 H decoupling is performed without signal enhancement by nuclear Overhauser effect. 6 . The process of claim 1 , wherein the upgrading comprises at least one of hydrotreating, hydrocracking and catalytic cracking.
by using nuclear magnetic resonance (G01N24/12 takes precedence) · CPC title
Aromatics · CPC title
Specific substances contained in the oils or fuels · CPC title
Gasoil having a boiling range of about 330 - 427 °C · CPC title
Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils (cracking in direct contact with molten metals or salts C10G9/34) · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.