Thermal pyoil to a gas fed cracker furnace
US-2024309276-A1 · Sep 19, 2024 · US
US10865349B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10865349-B2 |
| Application number | US-201816176679-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 31, 2018 |
| Priority date | Dec 19, 2017 |
| Publication date | Dec 15, 2020 |
| Grant date | Dec 15, 2020 |
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 invention relates to Delayed Coking of heavy petroleum residue producing petroleum coke and lighter hydrocarbon products. The invented process utilizes a pre-cracking reactor for mild thermal cracking of the feedstock and intermediate multistage separation system before being subjected to higher severity thermal cracking in delayed coking process, resulting in reduction in overall coke yield.
Opening claim text (preview).
The invention claimed is: 1. A method of reducing overall coke yield in a delayed coking process, said method comprising the steps of: a) passing a fresh hydrocarbon feed to a bottom of a main fractionator and mixing with internal recycle to make a secondary hydrocarbon feedstock; b) heating the secondary hydrocarbon feedstock in a furnace to obtain hot feed at a desired inlet temperature of a pre-cracking reactor; c) passing the hot feed at the desired inlet temperature and a pressure to the pre-cracking reactor, wherein the hot feed undergoes mild thermal cracking reactions to obtain an outlet product material stream; d) introducing the outlet product material stream to a first intermediate separator to split hydrocarbons in the outlet material stream into a first top product and bottom fractions, wherein the first top product comprises lighter products and gases and the bottom fractions is split into a first portion and a second portion; e) routing the first top product to the main fractionator; f) separating a first portion of the bottom fractions in a second intermediate separator column operating at vacuum conditions to obtain a second top product and a heavier bottom product; g) passing the second top product obtained in step (f) to the main fractionator; h) withdrawing the heavier bottom product from the second intermediate separator column of step (f) and passing to the main fractionator, wherein the heavier bottom product comprises Light Vacuum Gas Oil (LVGO) and Heavy Vacuum Gas Oil (HVGO); i) mixing the second portion from the first intermediate separator of step (d) and the heavier bottom product from the second intermediate separator column of step (f) and heating in a furnace to a desired coking temperature to obtain a hot hydrocarbon stream; j) passing the hot hydrocarbon stream from the furnace to a preheated coke drum; and k) passing product vapors exiting the coke drum to the main fractionator column to obtain product fractions. 2. The method as claimed in claim 1 , wherein in step (a) the fresh hydrocarbon feedstock is heated directly in the furnace. 3. The method as claimed in claim 1 , wherein a vacuum gasoil range cut is withdrawn from the second intermediate separator column and passed to secondary processing units, wherein the secondary processing units are selected from fluid catalytic cracking, hydrocracker and/or hydrotreater units. 4. The method as claimed in claim 1 , wherein the second top product from the second intermediate separator column is routed to at least one of product treatments units and the secondary processing unit. 5. The method as claimed in claim 1 , wherein the heavier bottom product are passed to secondary processing units. 6. The method as claimed in claim 5 , wherein a single stream is withdrawn from the second intermediate separator column and passed to the secondary processing units. 7. The method as claimed in claim 1 , wherein the product fractions comprise off-gas with LPG and naphtha, Kerosene, Light Coker Gas Oil (LCGO), Heavy Coker Gas Oil (HCGO), and heavy bottom product. 8. The method as claimed in claim 1 , wherein the heavy bottom product from the main fractionator is routed to the second intermediate separator. 9. The method as claimed in claim 1 , wherein the heavier bottom product are withdrawn from the second intermediate separator and passed to secondary processing units, wherein the secondary processing units comprises at least one of fluid catalytic cracking, hydrocracker, and/or hydrotreater units. 10. The method as claimed in claim 1 , wherein the pre-cracking reactor operates at the desired temperature in the range of 350 to 470° C. and the pressure in the range of 1 to 15 Kg/cm 2 (g). 11. The method as claimed in claim 1 , wherein feedstock within the pre-cracking reactor has a residence time in the range of 1 to 40 minutes. 12. The method as claimed in claim 1 , wherein the first intermediate separator is operated at a pressure in the range of 1 to 6 Kg/cm 2 (g). 13. The method as claimed in claim 1 , wherein the first intermediate separator is operated at a bottom temperature in the range of 300 to 400° C. 14. The method as claimed in claim 1 , wherein the second intermediate separator column is operated at a pressure in the range of pressure of 10 to 200 mmHg. 15. The method as claimed in claim 1 , wherein the second intermediate separator column is operated at a bottom temperature in the range of 200 to 350° C. 16. The method as claimed in claim 1 , wherein the coke drum is operated at a temperature in the range of 470 to 520° C. and a pressure in the range of 0.5 to 5 Kg/cm 2 (g). 17. The method as claimed in claim 1 , wherein feedstock within the coke drum is provided with a residence time of more than 10 hours for thermal cracking reactions. 18. The method as claimed in claim 7 , wherein the heavy bottom product is Coker Fuel Oil (CFO). 19. A method of reducing overall coke yield in a delayed coking process, said method comprising the steps of: a) heating a hydrocarbon feedstock in a furnace to obtain a hot feed at a desired inlet temperature of a pre-cracking reactor; b) passing the hot feed at the desired inlet temperature and a pressure to the pre-cracking reactor, wherein the hot feed undergoes mild thermal cracking reactions to obtain an outlet product material stream; c) introducing the outlet product material stream to a first intermediate separator to split hydrocarbons in the outlet material stream into a first top product and bottom fractions; d) routing the first top product to a main fractionator; e) separating the bottom fractions in a second intermediate separator column operating at vacuum conditions to obtain a second top product, a heavier bottom product and a heavy bottom material, wherein the heavy bottom product comprises of Coker Fuel Oil (CFO); f) passing the second top product obtained in step (e) to the main fractionator; g) withdrawing the heavier bottom product from the second intermediate separator of step (e) and passing to the main fractionator, wherein the heavier bottom product comprises Light Vacuum Gas Oil (LVGO) and Heavy Vacuum Gas Oil (HVGO); h) heating the heavy bottom material in a furnace to a desired coking temperature to obtain a hot hydrocarbon stream; i) passing the hot hydrocarbon stream from the furnace to a preheated coke drum; and j) passing product vapors exiting the coke drum to the main fractionator column to obtain product fractions.
Coking mineral oils, bitumen, tar, and the like or mixtures thereof with solid carbonaceous material (cracking oils C10G) · CPC title
according to the "fluidised-bed" technique · CPC title
Vacuum residues · CPC title
Atmospheric residues having a boiling point of at least about 538 °C · CPC title
Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions (C10G15/00 takes precedence; destructive hydrogenation of non-melting solid carbonaceous or similar materials C10G1/06) · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.