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Initial high sulfur levels of a hydrocarbon feedstock are reduced to desired low levels without the need for integration of substantial new equipment or hardware with existing hydroprocessing reactors. Ionic liquids are utilized as organic sulfur extraction agents and are added to and mixed with the

Initial high sulfur levels of a hydrocarbon feedstock are reduced to desired low levels without the need for integration of substantial new equipment or hardware with existing hydroprocessing reactors. Ionic liquids are utilized as organic sulfur extraction agents and are added to and mixed with the hydrocarbon feedstock containing organosulfur compounds downstream of an existing cold separator vessel. The ionic liquid and hydrocarbon mixture is maintained in a contact vessel under conditions which promote the formation of ionic sulfur-containing derivatives that are soluble in the ionic liquid to be formed, thereby enabling extractive removal and separation of the organosulfur compounds from the feedstock.

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1. A process to reduce the sulfur and nitrogen content of a hydrocarbon oil feedstock containing organosulfur compounds and organonitrogen compounds, the process comprising: a. introducing the hydrocarbon oil feedstock and hydrogen gas to a catalytic reactor;b. conveying a catalytic reactor effluent

1. A process to reduce the sulfur and nitrogen content of a hydrocarbon oil feedstock containing organosulfur compounds and organonitrogen compounds, the process comprising: a. introducing the hydrocarbon oil feedstock and hydrogen gas to a catalytic reactor;b. conveying a catalytic reactor effluent stream to a high pressure separator to separate a hydrogen stream and a mixed high pressure separator effluent, the mixed high pressure separator effluent including hydrogen sulfide, ammonia, and a hydroprocessed hydrocarbon mixture having a reduced organosulfur compound content and a reduced organonitrogen compound content;c. contacting the mixed high pressure separator effluent with water;d. conveying the mixed high pressure separator effluent containing water to a low pressure separator for separating the hydroprocessed hydrocarbon mixture from the mixed high pressure separator effluent,e. removing water from the low pressure separator;f. purging hydrogen sulfide and ammonia from the low pressure separator;g. conveying the separated hydroprocessed hydrocarbon mixture to a contact vessel;h. introducing ionic liquid into the separated hydroprocessed hydrocarbon mixture, wherein the ionic liquid and the hydroprocessed hydrocarbon mixture are retained in the contact vessel for a time sufficient for extractive removal of organosulfur compounds to create hydrocarbons and ionic sulfur-containing derivatives soluble in the ionic liquid, and for extractive removal of organonitrogen compounds to create hydrocarbons and ionic nitrogen-containing derivatives soluble in the ionic liquid;i. conveying the ionic liquid stream from the contact vessel to a vacuum distillation unit, the ionic liquid stream including ionic liquid, ionic sulfur-containing derivatives, ionic nitrogen-containing derivatives, and hydrocarbons;j. recovering a regenerated ionic liquid stream from the vacuum distillation unit;k. recovering a hydrocarbon stream from the vacuum distillation unit;l. conveying a hydrocarbon stream from the contact vessel to a fractionator, the hydrocarbon stream including an ionic liquid treated hydrocarbon mixture having a further reduced organosulfur compound content due to extractive removal and a further reduced organonitrogen compound content due to extractive removal, ionic liquid, ionic sulfur-containing derivatives soluble in the ionic liquid, and ionic nitrogen-containing derivatives soluble in the ionic liquid;m. recovering a fractionator bottoms stream containing ionic liquid, ionic sulfur-containing derivatives and ionic nitrogen-containing derivatives from the fractionator; andn. recovering a fractionator tops stream comprising the ionic liquid treated hydrocarbon mixture. 2. The process as in claim 1, wherein contacting the mixed high pressure separator effluent is by introducing the ionic liquid into a conduit between the low pressure separator and the contact vessel. 3. The process as in claim 2, wherein the ionic liquid and the hydroprocessed hydrocarbon mixture remain in contact within the conduit and/or within the contact vessel. 4. The process as in claim 1, wherein contacting the separated hydroprocessed hydrocarbon mixture is at a temperature sufficient to reduce the sulfur and nitrogen content. 5. The process as in claim 1, wherein the ratio of ionic liquid to feedstock is about 1:4 to about 1:25. 6. The process as in claim 1, wherein the ratio of ionic liquid to feedstock is about 1:6 to about 1:20. 7. The process as in claim 1, wherein the catalytic reactor is a hydrotreating reactor. 8. The process as in claim 1, wherein the catalytic reactor is a hydrocracking reactor. 9. The process as in claim 1, wherein the ionic liquid is an ionic liquid having a boiling point greater than about 425° C. 10. The process as in claim 1, wherein the hydrocarbon feedstock is a hydrocarbon fraction boiling in the range of about 36° C. to about 520° C. 11. The process as in claim 1, wherein the hydrocarbon feedstock is a hydrocarbon fraction boiling in the range of about 36° C. to about 370° C. 12. The process as in claim 1, wherein the ionic liquid is a non-aqueous ionic liquid of the general formula Q+A31 . 13. The process as in claim 12, wherein the A−ion is selected from the group consisting of halide anions, nitrate, sulfate, phosphate, acetate, haloacetates, tetrafluoroborate, tetrachloroborate, hexafluorophosphate, hexafluoroantimonate, fluorosulfonate, alkyl sulfonates, perfluoroalkyl sulfonates, bis(perfluoroalkylsulfonyl) amides, tris-trifluoromethanesulfononyl methylide of the formula C(CF3SO2)3−, unsubstituted arenesulfonates, arenesulfonates substituted by halogen or haloalkyl groups, the tetraphenylborate anion and the tetraphenylborate anions having substituted aromatic cores. 14. The process as in claim 12, wherein the Q+ ion is an ammonium cation, a phosphonium cation or a sulfonium cation. 15. The process as in claim 12, wherein the Q+ ion has the general formula NR1R2R3R4+ wherein R1, R2, R3 and R4 are the same or different and are selected from hydrogen and hydrocarbon radicals having from 1 to 30 carbon atoms, with the exception of an NH4+ cation. 16. The process as in claim 12, wherein the Q+ ion has the general formula PR1R2R3R4+ wherein R1, R2, R3 and R4 are the same or different and are selected from hydrogen and hydrocarbon radicals having from 1 to 30 carbon atoms. 17. The process as in claim 12, wherein the Q+ ion has the general formula R1R2N═CR3R4+ wherein R1, R2, R3 and R4 are the same or different and are selected from hydrogen and hydrocarbon radicals having from 1 to 30 carbon atoms. 18. The process as in claim 12, wherein the Q+ ion has the general formula R1R2P═CR3R4+ wherein R1, R2, R3 and R4 are the same or different and are selected from hydrogen and hydrocarbon radicals having from 1 to 30 carbon atoms. 19. The process as in claim 12, wherein the Q+ ion has the general formula R1R2P═CR3R4+ wherein R1, R2, R3 and R4 are the same or different and are selected from hydrogen and hydrocarbon radicals having from 1 to 30 carbon atoms. 20. The process as in claim 12, wherein the Q+ ion is a nitrogen-containing heterocyclic compound that includes 1, 2 or 3 nitrogen and atoms having cyclic compounds containing 4 to 10 atoms. 21. The process as in claim 20, wherein the Q+ ion has the general structural formula selected from the group consisting of wherein R1, R2, R3, R4 and R5 are the same or different and represent hydrogen or hydrocarbonyl radicals that have 1 to 30 carbon atoms. 22. The process as in claim 12, wherein the Q+ ion is a phosphorous-containing compound. 23. The process as in claim 22, wherein the Q+ ion has the general structural formula selected from the group consisting of 24. The process as in claim 12, wherein the Q+ ion has the general structural formula selected from the group consisting of R1R2+N═CR3—R5—R3C═N+R1R2, andR1R2+P═CR3—R5—R3C═P+R1R2 in which R1, R2 and R3, are the same or different, and represent hydrogen or hydrocarbonyl radicals that have 1 to 30 carbon atoms and R5 represents an alkylene radical or a phenylene radical. 25. The process as in claim 12, wherein the Q+ ion has is a sulfonium ion having the general formula: SR1R2R3+, where R1, R2 and R3, are the same or different hydrocarbonyl radicals having 1 to 12 carbon atoms. 26. The process as in claim 1, wherein the ionic liquid is selected from the group of ionic liquids consisting of N-butyl-pyridinium hexafluorophosphate, N-ethyl-pyridinium tetrafluoroborate, pyridinium fluorosulfonate, butyl-3-methyl-1-imidazolium tetrafluoroborate, butyl-3-methyl-1-imidazolium bis-trifluoromethane-sulfonyl amide, triethylsulfonium bis-trifluoromethane sulfonyl amide, butyl-3-methyl-1-imidazolium hexafluoro-antimonate, butyl-3-methyl-1-imidazolium hexafluorophosphate, butyl-3-methyl-1-imidazolium trifluoroacetate, butyl-3-methyl-1-imidazolium trifluoromethylsulfonate, butyl-3-methyl-1-imidazolium bis(trifluoromethylsulfonyl)-amide, trimethyl-phenylammonium hexafluorophosphate, tetrabutylphosphonium tetrafluoroborate, and combinations comprising at least one of these ionic liquids. 27. The process as in claim 1, wherein at least a portion of the regenerated ionic liquid recovered from the vacuum distillation unit is mixed with the ionic liquid in step (h) prior to the introduction of ionic liquid into the separated hydroprocessed hydrocarbon mixture. 28. The process as in claim 1, wherein at least a portion of the ionic liquid recovered from the fractionator bottoms stream is mixed with the ionic liquid in step (h) prior to the introduction of ionic liquid into the separated hydroprocessed hydrocarbon mixture.