US2014027345A1PendingUtilityA1
Vacuum gas oil conversion process
Est. expiryJul 30, 2032(~6 yrs left)· nominal 20-yr term from priority
C10G 69/06C10G 69/04C10G 2300/307C10G 45/08C10G 51/04C10G 69/02C10G 2300/1074C10G 2400/02C10G 11/05C10G 2400/04
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Claims
Abstract
An integrated thermal and catalytic process for improving the yield of middle distillate from heavy petroleum oil feeds comprises cracking the heavy portion (345° C.+) of the feed in a thermal conversion zone, followed by hydrotreating the thermally cracked product and the lighter portion of the feed and then separating the hydrotreated product into a bottoms fraction which is passed to a catalytic cracking step.
Claims
exact text as granted — not AI-modified1 . A thermal and catalytic process for converting a heavy petroleum oil feed into lower boiling products, comprising:
separating a heavy hydrocarbon feed to form a light fraction boiling below about 345° C. (650° F.) and a heavy fraction boiling above about 345° C. (650° F.); thermally cracking the heavy fraction in a thermal conversion zone to produce a thermally cracked product; combining the light fraction with the thermally cracked heavy fraction; hydrotreating the combined light and heavy fractions; separating the hydrotreated product in a fractionator into a hydrotreated bottoms fraction and a hydrotreated light fraction; catalytically cracking at least a portion of the hydrotreated bottoms fraction; and fractionating the catalytically cracked product to separate a naphtha fraction, a distillate fraction and a bottoms fraction.
2 . The process according to claim 1 , wherein the heavy hydrocarbon feed comprises a gas oil feed having a boiling point above 290° C.
3 . The process according to claim 2 , wherein the gas oil feed comprises a vacuum gas oil in which at least 75 wt % of the gas oil feed boils in the range of 345° to 565° C. (ASTM D 2887).
4 . The process according to claim 3 , wherein the gas oil feed comprises a vacuum gas oil in which at least 90 wt % of the gas oil feed boils in the range of 345° to 565° C. (ASTM D 2887).
5 . The process according to claim 2 , wherein the gas oil feed comprises up to 10 wt % of a resid boiling above 565° C.
6 . The process according to claim 4 , wherein the gas oil feed comprises up to 10 wt % of a resid boiling above 565° C.
7 . The process according to claim 1 , wherein the C 4 − fraction of the combined hydrotreated light and heavy fractions is by-passed around the hydrotreating step.
8 . The process according to claim 1 , wherein the severity of the thermal cracking step is from 25 to 450 equivalent seconds at 470° C.
9 . The process according to claim 4 , wherein the severity of the thermal cracking step is from 25 to 450 equivalent seconds at 470° C.
10 . The process according to claim 1 , wherein the hydrotreating step includes the following conditions: 6,000 to 10,000 kPag (about 870-1450 psig) hydrogen pressure, liquid hourly space velocity (LHSV) of 0.2-0.8 hr −1 and a temperature of from 355 to 455° C. (670 to 850° F.).
11 . The process according to claim 10 , wherein the hydrotreating step includes a hydrotreating catalyst containing at least one Group 6 metal and at least one Group 8-10 metal on a metal oxide support.
12 . The process according to claim 11 , wherein the metal oxide support is selected from silica, alumina, silica-alumina, and titania.
13 . The process according to claim 1 , wherein the catalytic cracking step includes the following conditions: temperatures from about 482 to about 740° C. (900 to 1364° F.); hydrocarbon partial pressures from about 70 to 300 kPaa (about 15 to about 43 psia); a catalyst to feed (wt/wt) ratio from about 3 to about 1, and a riser reactor residence time from 1 to 5 seconds.
14 . The process according to claim 13 , wherein the catalytic cracking step includes a cracking catalyst containing an amorphous, porous solid acid matrix selected from alumina, silica-alumina, silica-magnesia, silica-zirconia, silica-thoria, silica-beryllia, silica-titania, and silica-alumina-rare earth; and a zeolite.
15 . The process according to claim 1 , wherein the distillate fraction has a Cetane Number of at least 45.
16 . The process according to claim 5 , wherein the gas oil feed has a Conradson Carbon Residue (CCR) content greater than 1 wt %.
17 . The process according to claim 6 , wherein the gas oil feed has a Conradson Carbon Residue (CCR) content greater than 1 wt %.
18 . The process according to claim 1 , wherein at least a portion of the naphtha fraction is recycled back to the catalytic cracking step.
19 . The process according to claim 1 , wherein at least a portion of the bottoms fraction is recycled back to the catalytic cracking step.
20 . The process according to claim 18 , wherein at least a portion of the bottoms fraction is recycled back to the catalytic cracking step.Join the waitlist — get patent alerts
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