US2011024328A1PendingUtilityA1
Distillate production in a hydrocarbon synthesis process.
Est. expiryJul 31, 2029(~3 yrs left)· nominal 20-yr term from priority
C10G 47/00C10G 69/00C10G 65/14C10G 65/12
35
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Claims
Abstract
A wax fraction from a hydrocarbon synthesis process is fractionated in a vacuum distillation column prior to any hydrocracking steps. A straight-run distillation fraction is isolated from the vacuum distillation. A heavy wax fraction from the vacuum distillation process is hydroprocessed, and a hydroprocessed distillate fraction is recovered. The straight-run distillate fraction and the hydroprocessed distillate fraction are combined to make a fraction that boils in the range of diesel fuel.
Claims
exact text as granted — not AI-modified1 . A process for producing a distillate fuel, comprising;
a. passing a heavy fraction from a hydrocarbon synthesis process to a vacuum distillation zone and recovering at least a first distillate fuel fraction and a heavy wax fraction; b. passing the heavy wax fraction in combination with hydrogen to a hydrocracking reaction zone for cracking the carbon chain molecules in the heavy wax fraction to shorter molecules; and c. recovering a first reaction zone effluent from the hydrocracking reaction zone.
2 . The process of claim 1 , further comprising:
a. passing a combination of the first reaction zone effluent and a light fraction from the hydrocarbon synthesis process to a hydrotreating reaction zone; and b. recovering a second reaction zone effluent from the hydrotreating reaction zone.
3 . The process of claim 2 , further comprising passing a portion of the second reaction zone effluent to an atmospheric distillation zone and recovering at least a second distillate fuel fraction.
4 . The process of claim 3 , further comprising combining the first distillate fuel fraction and the second distillate fuel fraction to make a combined distillate fuel.
5 . The process of claim 4 , further comprising passing the combined distillate fuel to a hydroisomerization reaction zone for decreasing the cloud point of the combined distillate fuel.
6 . The process of claim 1 , further comprising:
a. passing the first reaction zone effluent from the hydrocracking reaction zone to a hydroisomerization reaction zone and producing a hydroisomerization reaction zone effluent; and b. passing at least a portion of the hydroisomerization reaction zone effluent to a hydrotreating reaction zone.
7 . A process for producing a distillate fuel from a hydrocarbon synthesis process, comprising:
a. passing a heavy fraction from a hydrocarbon synthesis process in combination with a hydroprocessed bottoms product to a vacuum distillation zone and recovering at least a first distillate fuel and a heavy wax stream therefrom; b. passing at least a portion of the heavy wax stream in combination with hydrogen to a hydrocracking reaction zone for cracking the carbon chain molecules in the wax product to shorter molecules, and recovering a first reaction zone effluent; c. combining a light fraction from the hydrocarbon synthesis process with at least a portion of the first reaction zone effluent and passing the combined feed, in further combination with hydrogen, to a hydrotreating reaction zone for hydrotreating the combined feed, and recovering a second reaction zone effluent; d. passing at least a portion of the second reaction zone effluent to an atmospheric distillation zone and recovering at least a second distillate fuel and the hydroprocessed bottoms product; and e. combining the first distillate fuel with the second distillate fuel to form a combined distillate fuel.
8 . The process of claim 7 , wherein the hydrocarbon synthesis process is a Fischer-Tropsch process.
9 . The process of claim 7 , wherein the hydrocracking reaction zone contains one or more catalysts, each comprising a cracking component and a hydrogenation component on an oxide support material.
10 . The process of claim 9 wherein the cracking component is selected from the group consisting of silica-alumina, Y-type zeolite, ultrastable Y-type zeolite and dealuminated zeolite.
11 . The process of claim 9 , wherein the hydrogenation component comprises at least one metal component selected from the Group VIII elements and/or from the Group VI elements.
12 . The process of claim 11 , wherein the Group VIII elements are selected from the group consisting of iron, cobalt, nickel, palladium and platinum.
13 . The process of claim 11 , wherein the Group VI elements are selected from the group consisting of chromium, molybdenum and tungsten.
14 . The process of claim 7 , wherein the hydrotreating reaction zone contains one or more catalysts, each comprising a composite of a Group VI metal or compound thereof with a Group VIII metal or compound thereof supported on a refractory base.
15 . The process of claim 14 , wherein the Group VIII elements are selected from the group consisting of iron, cobalt, nickel, palladium and platinum.
16 . The process of claim 14 , wherein the Group VI elements are selected from the group consisting of chromium, molybdenum and tungsten.
17 . The process of claim 14 , wherein the refractory base is alumina.
18 . The process of claim 7 , wherein the atmospheric distillation zone is maintained at a pressure in the range of greater than 15 psia to 150 psia.
19 . The process of claim 7 , wherein the vacuum distillation zone is maintained at a pressure of less than 15 psia.
20 . The process of claim 7 , wherein the combined distillate fuel has a normal boiling point range in the range of 350° F. to 750° F.
21 . The process of claim 7 , wherein the combined distillate fuel is a diesel fuel.
22 . The process of claim 7 , wherein the hydrocracking reaction zone and the hydrotreating reaction zone are in a single reactor vessel.
23 . The process of claim 7 , wherein the hydrocracking reaction zone and the hydrotreating reaction zone are in separate reactor vessels.
24 . The process of claim 7 , wherein the hydrocracking reaction zone is maintained at a pressure in the range of 200 to 4000 psig and at a temperature in the range of 600° F. to 900° F.
25 . The process of claim 7 , wherein the hydrotreating reaction zone is maintained at a pressure in the range of 200 to 4000 psig and at a temperature in the range of 400° F. to 850° F.Join the waitlist — get patent alerts
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