US2006058174A1PendingUtilityA1
Highly active slurry catalyst composition
Est. expirySep 10, 2024(expired)· nominal 20-yr term from priority
C07F 11/005C10G 45/08C10G 47/26C10G 2300/1033C10G 2300/1022B01J 27/049C10G 49/12C10G 45/04C10G 2300/1074C10G 2300/703C10G 49/04C07F 15/045C10G 2300/207Y10S502/517C10G 45/16B01J 37/20C10G 49/02C10G 2300/1003B01J 27/0515Y10T428/2982B01J 27/02B01J 31/00C10G 47/02B01J 35/27
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Claims
Abstract
The instant invention is directed to the preparation of a slurry catalyst composition. The slurry catalyst composition is prepared in a series of steps, involving mixing a Group VIB metal oxide and aqueous ammonia to form an aqueous mixture and sulfiding the mixture to form a slurry. The slurry is then promoted with a Group VIII metal. Subsequent steps involve mixing the slurry with a hydrocarbon oil, and combining the resulting mixture with hydrogen gas (under conditions which maintain the water in a liquid phase) to produce the active slurry catalyst.
Claims
exact text as granted — not AI-modified1 . A catalyst composition suitable for the hydroconversion of heavy oils, which is prepared by:
(a) mixing a Group VI B metal oxide and aqueous ammonia to form a Group VI B metal compound aqueous mixture; (b) sulfiding, in a first reaction zone, the aqueous mixture of step (a) with a gas comprising hydrogen sulfide to a dosage greater than 8 SCF of hydrogen sulfide per pound of Group VI B metal to form a slurry; (c) promoting the slurry with a Group VIII metal compound; (d) mixing the slurry of step (c) with hydrocarbon oil having a viscosity of at least 2 cSt @ 212° F. to form Mixture X; (e) combining Mixture X with hydrogen gas in a second reaction zone, under conditions which maintain the water in Mixture X in a liquid phase, thereby forming an active catalyst composition admixed with a liquid hydrocarbon; and (f) recovering the active catalyst composition.
2 . The catalyst composition of claim 1 , wherein conditions in the first reaction zone comprise a temperature in the range from at least about 80° F. to about 200° F., and a pressure in the range from at least about 100 psig to about 3000 psig.
3 . The catalyst composition of claim 2 , wherein conditions in the first reaction zone comprise a temperature in the range from at least about 100° F. to about 180° F., and a pressure in the range from at least about 200 psig to about 1000 psig.
4 . The catalyst composition of claim 3 , wherein conditions in the first reaction zone comprise a temperature in the range from at least about 130° F. to about 160° F. and a pressure in the range from at least about 300 psig to about 500 psig.
5 . The catalyst composition of claim 1 , wherein the hydrocarbon oil viscosity ranges from at least about 2 cSt @ 212° F. to about 15 cSt @ 212° F.
6 . The catalyst composition of claim 1 , wherein the Group VIII metal compound of step (c) is selected from the group consisting of nickel sulfates and cobalt sulfates.
7 . The catalyst composition of claim 20 , wherein high shear mode occurs, in the range from 100 RPM to 1600 RPM.
8 . The catalyst composition of claim 6 , in which the weight ratio of nickel or cobalt to Group VI B metal oxide ranges from 1:100 to about 1:2.
9 . The catalyst composition of claim 1 , wherein the ratio of Group VI B metal oxide to oil is at least less than 1.0.
10 . The catalyst composition of claim 1 , wherein the hydrocarbon oil is a vacuum gas oil.
11 . The catalyst composition of claim 1 , wherein the conditions of the second reaction zone comprise a temperature in the range from at least about 350° F. to about 600° F. and a pressure in the range from at least about 100 psig to about 3000 psig.
12 . The catalyst composition of claim 11 , wherein the conditions of the second reaction zone comprise a temperature in the range from at least about 350° F. to about 600° F. and the pressure in the range from at least about 200 psig to about 1000 psig.
13 . The compositions of claim 12 , wherein hydrogen is continuously added to the second reaction zone, and high shear mixing is employed in order to maintain a homogenous slurry.
14 . The catalyst composition of claim 1 , which is recovered by means of a high pressure separator.
15 . The catalyst composition of claim 1 , which exist in an active and concentrated state.
16 . The catalyst of claim 14 , which is continuously mixed in a storage tank to maintain a homogenous slurry.
17 . The catalyst composition of claim 9 , wherein the ratio of Group VI B metal oxide to oil is at least less than 0.5.
18 . The catalyst composition of claim 17 , wherein the ratio of Group VI B metal oxide to oil is at least less than 0.1.
19 . The catalyst composition of claim 8 , wherein the Group VI B metal is selected from the group consisting of tungsten and molybdenum.
20 . A catalyst composition suitable for the hydroconversion of heavy oils, which is prepared by:
(a) mixing a Group VI B metal oxide and aqueous ammonia to form a Group VI B metal compound aqueous mixture; (b) sulfiding, in a first reaction zone, the aqueous mixture of step (a) with a gas comprising hydrogen sulfide to a dosage greater than 8 SCF of hydrogen sulfide per pound of Group VI B metal to form a slurry; (c) promoting the slurry with a Group VIII metal compound; (d) mixing, at high shear mode, the slurry of step (c) with a first hydrocarbon oil having a viscosity of at least 2 cSt @ 212° F. to form Mixture X; (e) combining Mixture X at high shear mode with hydrogen gas in a second reaction zone, under conditions which maintain the water in Mixture X in a liquid phase, thereby forming an active catalyst composition admixed with a liquid hydrocarbon; and (f) recovering the active catalyst composition.Join the waitlist — get patent alerts
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