US20040200759A1 - Sulfone removal process - Google Patents
Sulfone removal process Download PDFInfo
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- US20040200759A1 US20040200759A1 US10/411,796 US41179603A US2004200759A1 US 20040200759 A1 US20040200759 A1 US 20040200759A1 US 41179603 A US41179603 A US 41179603A US 2004200759 A1 US2004200759 A1 US 2004200759A1
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- United States
- Prior art keywords
- sulfur
- fossil fuel
- sulfones
- hydrodesulfurization
- present
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- 238000000034 method Methods 0.000 title claims abstract description 59
- 230000008569 process Effects 0.000 title claims abstract description 49
- 150000003457 sulfones Chemical class 0.000 title claims abstract description 36
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 57
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 53
- 239000011593 sulfur Substances 0.000 claims abstract description 53
- 239000002803 fossil fuel Substances 0.000 claims abstract description 37
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 claims abstract description 11
- 229910000037 hydrogen sulfide Inorganic materials 0.000 claims abstract description 10
- 150000001875 compounds Chemical class 0.000 claims description 14
- 239000007788 liquid Substances 0.000 claims description 14
- 238000006243 chemical reaction Methods 0.000 claims description 9
- 239000007800 oxidant agent Substances 0.000 claims description 8
- 150000004965 peroxy acids Chemical class 0.000 claims description 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 3
- 125000001741 organic sulfur group Chemical group 0.000 claims description 2
- 239000010779 crude oil Substances 0.000 abstract description 10
- 239000007789 gas Substances 0.000 abstract description 8
- 230000001590 oxidative effect Effects 0.000 description 28
- 238000006477 desulfuration reaction Methods 0.000 description 19
- 230000023556 desulfurization Effects 0.000 description 19
- 239000003054 catalyst Substances 0.000 description 9
- 238000002604 ultrasonography Methods 0.000 description 7
- 150000003464 sulfur compounds Chemical class 0.000 description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- 239000003208 petroleum Substances 0.000 description 5
- 238000012545 processing Methods 0.000 description 5
- 238000007670 refining Methods 0.000 description 5
- 239000000446 fuel Substances 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 238000000638 solvent extraction Methods 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- 239000002283 diesel fuel Substances 0.000 description 3
- 239000003502 gasoline Substances 0.000 description 3
- -1 naphtha Substances 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 239000003209 petroleum derivative Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 238000010924 continuous production Methods 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- IYYZUPMFVPLQIF-UHFFFAOYSA-N dibenzothiophene Chemical compound C1=CC=C2C3=CC=CC=C3SC2=C1 IYYZUPMFVPLQIF-UHFFFAOYSA-N 0.000 description 2
- 239000000295 fuel oil Substances 0.000 description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
- 229930192474 thiophene Natural products 0.000 description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 238000003916 acid precipitation Methods 0.000 description 1
- 238000003915 air pollution Methods 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000012993 chemical processing Methods 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- WHDPTDWLEKQKKX-UHFFFAOYSA-N cobalt molybdenum Chemical compound [Co].[Co].[Mo] WHDPTDWLEKQKKX-UHFFFAOYSA-N 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
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- 230000001627 detrimental effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000007730 finishing process Methods 0.000 description 1
- 238000004508 fractional distillation Methods 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- 231100000206 health hazard Toxicity 0.000 description 1
- 239000010763 heavy fuel oil Substances 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 150000002432 hydroperoxides Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000003278 mimic effect Effects 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- DDTIGTPWGISMKL-UHFFFAOYSA-N molybdenum nickel Chemical compound [Ni].[Mo] DDTIGTPWGISMKL-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- JTJMJGYZQZDUJJ-UHFFFAOYSA-N phencyclidine Chemical compound C1CCCCN1C1(C=2C=CC=CC=2)CCCCC1 JTJMJGYZQZDUJJ-UHFFFAOYSA-N 0.000 description 1
- 239000002952 polymeric resin Substances 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000002760 rocket fuel Substances 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 238000000956 solid--liquid extraction Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 150000003577 thiophenes Chemical class 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G67/00—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one process for refining in the absence of hydrogen only
- C10G67/02—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one process for refining in the absence of hydrogen only plural serial stages only
- C10G67/12—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one process for refining in the absence of hydrogen only plural serial stages only including oxidation as the refining step in the absence of hydrogen
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G27/00—Refining of hydrocarbon oils in the absence of hydrogen, by oxidation
- C10G27/04—Refining of hydrocarbon oils in the absence of hydrogen, by oxidation with oxygen or compounds generating oxygen
- C10G27/12—Refining of hydrocarbon oils in the absence of hydrogen, by oxidation with oxygen or compounds generating oxygen with oxygen-generating compounds, e.g. per-compounds, chromic acid, chromates
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G45/00—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds
- C10G45/02—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing
Definitions
- the present invention is directed to methods for generating and facilitating the removal of oxidized sulfur species, and in particular sulfones, from liquid fossil fuels.
- sulfur is a common impurity found on most crude oil, and is known to contribute to air pollution, most notably by contributing to the formation of acid rain, and is considered a health hazard.
- Such sulfur containing species are further known to cause corrosion in pipeline, pumping and refining equipment, and can further substantially decrease the life span catalysts used in refining and combustion of fossil fuels.
- hydrodesulfurization which involves subjecting fossil fuels to high temperatures and pressure in the presence of hydrogen and an inorganic catalyst.
- the organic sulfur is converted to hydrogen sulfide, which is further processed to yield elemental sulfur.
- Such process is deemed generally cost-effective to the extent the crude oil subjected to such process does not contain a heavy sulfur content or if the refined petroleum product meets existing sulfur levels, such as the current diesel sulfur content of 500 ppmw or less.
- An alternative approach to hydrodesulfurization is oxidative desulfurization.
- oxidative desulfurization involves oxidizing any sulfur species that may be present, typically through the use of an oxidizing agent, such as a hydroperoxide or peracid, to thus convert the sulfur compounds to sulfones.
- ultrasound may be applied as per the teachings of U.S. Pat. No. 6,402,939, issued to Yen et al., entitled “Oxidative Desulfurization of Fossil Fuels With Ultrasound”; and U.S. Pat. No. 6,500,219, issued to Gunnerman, entitled “Continuous Process for Oxidative Desulfurization of Fossil Fuels With Ultrasound and Products Thereof”, the teachings of each are expressly incorporated herein by reference.
- oxidative desulfurization can be performed under mild temperatures and pressures, and further typically does not require hydrogen. Additionally advantageous is the fact that oxidative desulfurization requires much less in terms of capital expenditures to implement. In this respect, oxidative desulfurization can be selectively deployed to treat only a single fraction of refined petroleum, such as diesel, and can be readily integrated as a finishing process into existing refinery facilities. Perhaps most advantageous is the fact that oxidative desulfurization can substantially eliminate all sulfur species present in a given amount of crude oil such that ultra-low sulfur levels can be attained, and in particular the lower standards being set forth in various legislative requirements regarding sulfur content levels.
- the present invention specifically addresses and alleviates the above-identified deficiencies in the art.
- the present invention provides the process for facilitating the removal of sulfur-containing species from crude oil and/or any fractions derived therefrom by subjecting the same to a first oxidative process whereby a majority, if not substantially all the sulfur-containing species present in such crude oil or fraction are converted to sulfones.
- any of a variety of conventional processes known in the art to effectuate oxidative desulfurization may be utilized.
- conventional chemical processing utilizing oxidizing agents, such as peracids, to sufficiently convert the sulfur species to sulfones may be utilized.
- ultrasound may be deployed to effectuate oxidation of substantially all of the sulfur containing species to sulfones.
- the resultant fossil fuel is subjected to conventional hydrodesulfurization.
- the sulfone-containing fossil fuel is fed directly to a conventional hydrotreater and thus subjected to conventional hydrodesulfurization processing, namely, elevated temperature, elevated pressure, and hydrogen gas in the presence of catalysts, such that a cobalt-molybdenum (Co/Mo) or nickel-molybdenum (Ni/Mo) catalyst, such that all the sulfur present in the sulfones are converted to hydrogen sulfide and thereafter removed through conventional processes.
- the gaseous hydrogen sulfide may converted to elemental sulfur via the Claus process.
- Substantially all of the sulfur species are removed from the fossil fuel as a result of process.
- the hydrodesulfurization need not be performed at substantially elevated, temperatures, pressures, or otherwise use a greater volume of catalysts, as is typically required to remove sulfur to 15 ppmw or less.
- the processes of the present invention are operative to substantially eliminate those sulfur compounds, such as aromatic, cyclic and condensed multicyclic sulfur compounds, that are less responsive to the hydrodesulfurization process alone.
- the process of the present invention eliminates those drawbacks associated with conventional oxidative desulfurization processing requiring the removal of sulfones produced thereby through solvent extraction or absorption.
- FIG. 1 is a flow chart illustrating the steps utilized in the sulfone removal process of the present invention.
- liquid fossil fuel is used herein to denote any carbonaceous liquid that is derived from petroleum, coal, or any other naturally occurring material that is used for energy generation for any kind of use, including industrial uses, commercial uses, governmental uses, and consumer uses.
- liquid fossil fuels expressly include automotive fuels, such as gasoline, diesel fuels, jet fuel, rocket fuel, as well as petroleum residuum based fuel oils including bunker fuels and residual fuels.
- such term includes any fraction derived from petroleum, namely, those fractions derived through conventional refining processes, and in particular fractional distillation.
- such fractions expressly include but are not limited to gas, naphtha, gasoline, kerosene, gas oil or diesel, lubricating oil, heavy gas or fuel oil, and residual, plus any and all products derived therefrom through further processing, such as through cracking, unification and alteration.
- FIG. I a flow chart diagram illustrating the steps necessary for practicing the same.
- Such process comprises the initial step of providing a fossil fuel 20 which, as discussed above, should be interpreted broadly.
- the fossil fuel provided in step 20 will comprise various fractions of the refined petroleum, and that diesel fuel will be particularly well suited for the practice of the present invention given the soon-to-be implemented requirements that mandate that diesel sulfur content be substantially minimized to levels of 15 ppmw or less.
- the fossil fuel provided in step 20 is then subjected to an oxidative reaction such that at least the majority, if not substantially all of the sulfur-containing compounds present in the liquid fossil fuel are converted to sulfones.
- sulfones are generally represented by the formula: R—S(O) 2 —R and can be produced via the oxidation of sulfides and sulfoxides via a variety of reactions well-known to those skilled in the art.
- sulfur-containing compounds present in the liquid fossil fuels may be oxidized via reactions with oxidizing agents, such as hydroperoxides and peracids.
- Exemplary of those types of processes operative to effectuate the conversion of the sulfur-containing compounds to sulfones include those oxidative desulfurization processes developed by the Lyondell Chemical Company which utilizes t-butylhydroperoxide as an oxidizing agent to convert sulfur-containing species present in a liquid fossil fuel, and in particular diesel, to sulfones using mild temperatures and pressures.
- Other known oxidative desulfurization processes include those processes disclosed in U.S. Pat. No. 6,402,939, issued to Yen et al., entitled “Oxidative Desulfurization of Fossil Fuels With Ultrasound”; and U.S. Pat. No.
- the oxidative process will be effective to oxidize those sulfur-containing compounds that are typically less responsive or otherwise nonreactive to hydrodesulfurization processing.
- oxidative reactions such as those utilized in oxidative desulfurization, are substantially effective in oxidizing aromatic sulfur compounds, cyclic sulfur compounds, and condensed multicyclic sulfur compounds, such as thiophene, benzothiophene, dibenzothiophene, and other condensed-ring thiophenes, which are typically resistant to hydrogenation via to hydrodesulfurization.
- hydrodesulfurization in step 40 can be conducted per conventional practices, such as those necessary to effectuate a sulfur content of approximately 500 ppmw, and need not utilize substantially elevated temperatures, elevated pressure, and/or increased catalyst volume, as is necessary to attain lower sulfur content levels utilizing the hydrodesulfurization process by itself.
- the hydrodesulfurization process is operative to convert virtually all of the sulfones readily into hydrogen sulfide gas.
- hydrodesulfurization by itself is typically inoperative to remove a wide variety of sulfur-containing compounds unless the same pre-exist in oxidized state as attained by prior oxidative process.
- the processes of the present invention eliminate the need to remove sulfones via conventional oxidative desulfurization practices, namely, solvent extraction or adsorption.
- refineries need not integrate such sulfone removal processes as part of their refining process, particularly at the expense of hydrodesulfurization.
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- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Abstract
Processes for generating and removing oxidized sulfur species, and in particular sulfones, from crude oil and various fractions derived therefrom. Initially, the sulfur species present in the crude oil or fractions derived from the crude oil, is oxidized such that substantially all of the sulfur species are converted to sulfones. Thereafter, the fossil fuel containing the oxidized sulfur species are subjected to conventional hydrodesulfurization processes where substantially all of the sulfones are converted to hydrogen sulfide gas.
Description
- Not Applicable
- Not Applicable
- The present invention is directed to methods for generating and facilitating the removal of oxidized sulfur species, and in particular sulfones, from liquid fossil fuels.
- In this respect, sulfur is a common impurity found on most crude oil, and is known to contribute to air pollution, most notably by contributing to the formation of acid rain, and is considered a health hazard.. Such sulfur containing species are further known to cause corrosion in pipeline, pumping and refining equipment, and can further substantially decrease the life span catalysts used in refining and combustion of fossil fuels.
- Due to its detrimental effects, legislation has been enacted to reduce sulfur content in refined petroleum products. Exemplary of such newly enacted standards include requirements set by the Environmental Protection Agency, pursuant to the Clean Air Act of 1964, that set an upper limit of 15 parts per million by weight (ppmw) of the sulfur content in ultra low sulfur diesel (ULSD) by Jun. 1, 2006. Similar requirements have been enacted in Europe and other industrialized countries, such as Japan.
- The process most widely utilized for removing sulfur present in crude oil fractions is hydrodesulfurization, which involves subjecting fossil fuels to high temperatures and pressure in the presence of hydrogen and an inorganic catalyst. Through such process, the organic sulfur is converted to hydrogen sulfide, which is further processed to yield elemental sulfur. Such process is deemed generally cost-effective to the extent the crude oil subjected to such process does not contain a heavy sulfur content or if the refined petroleum product meets existing sulfur levels, such as the current diesel sulfur content of 500 ppmw or less.
- To the extent hydrodesulfurization is utilized to reduce diesel sulfur content to substantially lower levels, namely, 15 ppmw or less, such process becomes substantially less effective it dramatically increases operating costs. In this regard, to hydro treat oil to attain such lower levels requires the use of substantially higher temperatures, higher pressures, and catalyst volume then is typically utilized. Indeed, even by utilizing such advanced hydrodesulfurization processes, substantially difficulties still arise in removing sulfur below 20 ppmw, as well as removing more difficult to remove sulfur compounds, such as aromatic, cyclic and condensed multicyclic sulfur compounds.
- An alternative approach to hydrodesulfurization is oxidative desulfurization. Essentially, such process involves oxidizing any sulfur species that may be present, typically through the use of an oxidizing agent, such as a hydroperoxide or peracid, to thus convert the sulfur compounds to sulfones. To facilitate such oxidative reaction, ultrasound may be applied as per the teachings of U.S. Pat. No. 6,402,939, issued to Yen et al., entitled “Oxidative Desulfurization of Fossil Fuels With Ultrasound”; and U.S. Pat. No. 6,500,219, issued to Gunnerman, entitled “Continuous Process for Oxidative Desulfurization of Fossil Fuels With Ultrasound and Products Thereof”, the teachings of each are expressly incorporated herein by reference.
- Advantageously, oxidative desulfurization can be performed under mild temperatures and pressures, and further typically does not require hydrogen. Additionally advantageous is the fact that oxidative desulfurization requires much less in terms of capital expenditures to implement. In this respect, oxidative desulfurization can be selectively deployed to treat only a single fraction of refined petroleum, such as diesel, and can be readily integrated as a finishing process into existing refinery facilities. Perhaps most advantageous is the fact that oxidative desulfurization can substantially eliminate all sulfur species present in a given amount of crude oil such that ultra-low sulfur levels can be attained, and in particular the lower standards being set forth in various legislative requirements regarding sulfur content levels.
- Despite the various benefits associated with the use of oxidative desulfurization, however, the utilization of such process to remove sulfur continues to be problematic in several respects. Of most concern is the ability to effectuate the removal of the sulfones from the fuel, which is typically achieved either through solvent extraction or absorption, based upon the differential polarity of the sulfones. With respect to absorbents, silica gel, activated alumina, polymeric resins, and zeolites can be utilized to effectuate solid-liquid extraction. With respect to solvent extraction, solvents such as dimethyl formaldehyde, N-methylpyrrolidone, or acetonitrile can be utilized. Alternatively, organic solvents that are either immiscible or marginally immiscible with the fossil fuel can be utilized.
- Such removal techniques, however, substantially complicate the sulfur removal process, and add considerably to the time and expense associated with oxidative desulfurization. As a result of the expense and complications associated with the sulfone removal step associated with oxidative desulfurization, oxidative desulfurization typically is only feasible for small to medium refinery operations.
- As such, there is a substantial need in the art for a process for effectuating the removal of sulfur from refined crude oil that is substantially effective in removing virtually all of the sulfur species present in the fossil fuel that is further extremely cost effective and can be readily integrated into conventional oil refining processes. There is an additional need for such a process that can be utilized in either large scale or small scale refinery operations that is further effective to achieve sulfur removal requirements to be implemented regarding the sulfur content of refined petroleum products, and in particular diesel fuel and gasoline.
- The present invention specifically addresses and alleviates the above-identified deficiencies in the art. Specifically, the present invention provides the process for facilitating the removal of sulfur-containing species from crude oil and/or any fractions derived therefrom by subjecting the same to a first oxidative process whereby a majority, if not substantially all the sulfur-containing species present in such crude oil or fraction are converted to sulfones. To accomplish that end, any of a variety of conventional processes known in the art to effectuate oxidative desulfurization may be utilized. In this respect, conventional chemical processing utilizing oxidizing agents, such as peracids, to sufficiently convert the sulfur species to sulfones may be utilized. Alternatively, or in addition to the use of oxidizing agents, ultrasound may be deployed to effectuate oxidation of substantially all of the sulfur containing species to sulfones.
- Once a substantial portion of the sulfur containing species have been converted to sulfones, the resultant fossil fuel is subjected to conventional hydrodesulfurization. In this respect, the sulfone-containing fossil fuel is fed directly to a conventional hydrotreater and thus subjected to conventional hydrodesulfurization processing, namely, elevated temperature, elevated pressure, and hydrogen gas in the presence of catalysts, such that a cobalt-molybdenum (Co/Mo) or nickel-molybdenum (Ni/Mo) catalyst, such that all the sulfur present in the sulfones are converted to hydrogen sulfide and thereafter removed through conventional processes. In this respect, the gaseous hydrogen sulfide may converted to elemental sulfur via the Claus process.
- Substantially all of the sulfur species are removed from the fossil fuel as a result of process. Advantageously, the hydrodesulfurization need not be performed at substantially elevated, temperatures, pressures, or otherwise use a greater volume of catalysts, as is typically required to remove sulfur to 15 ppmw or less. Additionally, the processes of the present invention are operative to substantially eliminate those sulfur compounds, such as aromatic, cyclic and condensed multicyclic sulfur compounds, that are less responsive to the hydrodesulfurization process alone. Furthermore, the process of the present invention eliminates those drawbacks associated with conventional oxidative desulfurization processing requiring the removal of sulfones produced thereby through solvent extraction or absorption.
- These as well as other features of the present invention will become more apparent upon reference to the drawings.
- FIG. 1 is a flow chart illustrating the steps utilized in the sulfone removal process of the present invention.
- The detailed description set forth below is intended as a description of the presently preferred embodiment of the invention, and is not intended to represent the only form in which the present invention may be constructed or utilized. The description sets forth the functions and sequences of steps for constructing and operating the invention. It is to be understood, however, that the same or equivalent functions and sequences may be accomplished by different embodiments and that they are also intended to be encompassed within the scope of the invention.
- In this regard, the present invention is directed to methods for effectuating the removal of sulfur-containing compounds from a liquid fossil fuel. At the outset, it should be recognized that the term “liquid fossil fuel” is used herein to denote any carbonaceous liquid that is derived from petroleum, coal, or any other naturally occurring material that is used for energy generation for any kind of use, including industrial uses, commercial uses, governmental uses, and consumer uses. In this respect, it should be understood that liquid fossil fuels expressly include automotive fuels, such as gasoline, diesel fuels, jet fuel, rocket fuel, as well as petroleum residuum based fuel oils including bunker fuels and residual fuels. It should be further understood that such term includes any fraction derived from petroleum, namely, those fractions derived through conventional refining processes, and in particular fractional distillation. In this respect, such fractions expressly include but are not limited to gas, naphtha, gasoline, kerosene, gas oil or diesel, lubricating oil, heavy gas or fuel oil, and residual, plus any and all products derived therefrom through further processing, such as through cracking, unification and alteration.
- With respect to the processes for effectuating the removal of sulfur from fossil fuels, there is depicted in FIG. I a flow chart diagram illustrating the steps necessary for practicing the same. Such process comprises the initial step of providing a
fossil fuel 20 which, as discussed above, should be interpreted broadly. Along these lines, it is contemplated that for most practical applications, the fossil fuel provided instep 20 will comprise various fractions of the refined petroleum, and that diesel fuel will be particularly well suited for the practice of the present invention given the soon-to-be implemented requirements that mandate that diesel sulfur content be substantially minimized to levels of 15 ppmw or less. - The fossil fuel provided in
step 20 is then subjected to an oxidative reaction such that at least the majority, if not substantially all of the sulfur-containing compounds present in the liquid fossil fuel are converted to sulfones. In this regard, sulfones are generally represented by the formula: R—S(O)2—R and can be produced via the oxidation of sulfides and sulfoxides via a variety of reactions well-known to those skilled in the art. In this respect, sulfur-containing compounds present in the liquid fossil fuels may be oxidized via reactions with oxidizing agents, such as hydroperoxides and peracids. Exemplary of those types of processes operative to effectuate the conversion of the sulfur-containing compounds to sulfones include those oxidative desulfurization processes developed by the Lyondell Chemical Company which utilizes t-butylhydroperoxide as an oxidizing agent to convert sulfur-containing species present in a liquid fossil fuel, and in particular diesel, to sulfones using mild temperatures and pressures. Other known oxidative desulfurization processes include those processes disclosed in U.S. Pat. No. 6,402,939, issued to Yen et al., entitled “Oxidative Desulfurization of Fossil Fuels With Ultrasound”; and U.S. Pat. No. 6,500,219, issued to Gunnerman, entitled “Continuous Process for Oxidative Desulfurization of Fossil Fuels With Ultrasound and Products Thereof”, the teachings of which are incorporated herein by reference, that deploy ultrasound in combination with hydroperoxide such that a substantial portion of the sulfur-containing compounds present in the liquid fossil fuel are converted to sulfones. - As will be appreciated by those skilled in the art, the oxidative process will be effective to oxidize those sulfur-containing compounds that are typically less responsive or otherwise nonreactive to hydrodesulfurization processing. In this respect, such oxidative reactions, such as those utilized in oxidative desulfurization, are substantially effective in oxidizing aromatic sulfur compounds, cyclic sulfur compounds, and condensed multicyclic sulfur compounds, such as thiophene, benzothiophene, dibenzothiophene, and other condensed-ring thiophenes, which are typically resistant to hydrogenation via to hydrodesulfurization.
- Once the sulfur-containing compounds have been sufficiently oxidized to convert the majority, if not substantially all, of such compositions to sulfones, such sulfone/fossil fuel mixture is subjected to conventional hydrodesulfurization. In this respect, such sulfone/liquid fossil fuel mixture is fed directly to a conventional hydrotreater to thus subject the sulfone/fossil fuel mixture to elevated temperature, elevated pressure, and hydrogen in the presence of a catalyst. In this regard, such hydrodesulfurization in
step 40 can be conducted per conventional practices, such as those necessary to effectuate a sulfur content of approximately 500 ppmw, and need not utilize substantially elevated temperatures, elevated pressure, and/or increased catalyst volume, as is necessary to attain lower sulfur content levels utilizing the hydrodesulfurization process by itself. - Once subjected to the hydrodesulfurization process, most, if not substantially all of the sulfones present in the liquid fossil fuel are converted to hydrogen sulfide gas via conventional hydrotreater processing. As is well-known to those skilled in the art, hydrogen sulfide gas is readily removed as part of the hydrodesulfurization process and can ultimately be converted to elemental sulfur. In this respect, the vast majority of refineries currently operating are provided with hydrotreater units that are operative to effectuate the hydrodesulfurization process, and hence isolate the hydrogen sulfide gas byproduct produced thereby. As such, the continuous implementation of hydrodesulfurization using conventional hydrotreaters will not result in increased capital expenditures necessary to practice the processes of the present invention
- Advantageously, however, by virtue of the fact that a substantial portion, if not all of the sulfur-containing compounds are oxidized to sulfones prior to being subjected to hydrodesulfurization, the hydrodesulfurization process is operative to convert virtually all of the sulfones readily into hydrogen sulfide gas. As discussed above, hydrodesulfurization by itself is typically inoperative to remove a wide variety of sulfur-containing compounds unless the same pre-exist in oxidized state as attained by prior oxidative process. At the same time, the processes of the present invention eliminate the need to remove sulfones via conventional oxidative desulfurization practices, namely, solvent extraction or adsorption. In this regard, by deploying hydrodesulfurization, as opposed to such conventional sulfone removal practices, refineries need not integrate such sulfone removal processes as part of their refining process, particularly at the expense of hydrodesulfurization.
- Additional modifications and improvements of the present invention may also be apparent to those of ordinary skill in the art. Along these lines, it is contemplated that the combination of an oxidative reaction followed by hydrodesulfurization (or any other reaction for that matter which subjects the liquid fossil fuel to increased temperature, increased pressure and hydrogen in the presence of a catalyst) may further be operative to effectuate the removal of other undesirable non-sulfur-containing compounds. For example, it is contemplated that those processes known or later developed in the art effectuating the oxidation of nitrogen-containing compounds may first be deployed followed by hydrodesulfurization such that the oxidized nitrogen-containing compounds become converted to ammonia. In this respect, it is contemplated that the removal of nitrogen will closely mimic the processes described herein for effectuating the removal of sulfur. Thus, the particular combination of parts and steps described and illustrated herein is intended to represent only certain embodiments of the present invention, and is not intended to serve as limitations of alternative devices and methods within the spirit and scope of the invention.
Claims (7)
1. A process for generating sulfones from sulfur-containing compounds present in a fossil fuel and thereafter removing said sulfones from said fossil fuel, the process comprising the steps:
a) providing a liquid fossil fuel, said fossil fuel containing a portion of at least one organic sulfur-containing compound;
b) converting a majority of said sulfur-bearing compound to a sulfone; and
c) subjecting said fossil fuel produced in step b) to hydrodesulfurization such that a majority of the sulfones present in such fossil fuel are converted to hydrogen sulfid.
2. The method of claim 1 wherein step c), said hydrodesulfurization process is conducted in a conventional hydrotreater.
3. The method of claim I wherein in step b), said sulfur-containing compound is oxidized by an oxidizing agent.
4. The method of claim 3 wherein said oxidizing agent comprises a hydroperoxide.
5. The method of claim 3 wherein said oxidizing agent comprises a peracid.
6. The method of claim 1 wherein in step b), said conversion comprises subjecting said fossil fuel to an ultrasonic energy.
7. The method of claim 1 wherein said process further comprises the steps:
a) removing said hydrogen sulfide produced in step c) from said liquid fossil fuel; and
b) converting said hydrogen sulfide removed in step d) to elemental sulfur.
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| US10/411,796 US20040200759A1 (en) | 2003-04-11 | 2003-04-11 | Sulfone removal process |
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| US10/411,796 US20040200759A1 (en) | 2003-04-11 | 2003-04-11 | Sulfone removal process |
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| US20070051667A1 (en) * | 2005-09-08 | 2007-03-08 | Martinie Gary M | Diesel oil desulfurization by oxidation and extraction |
| US20100140142A1 (en) * | 2008-12-10 | 2010-06-10 | Chevron U.S.A. Inc. | Removing unstable sulfur compounds from crude oil. |
| US20100300938A1 (en) * | 2005-09-08 | 2010-12-02 | Martinie Gary D | Process for oxidative conversion of organosulfur compounds in liquid hydrocarbon mixtures |
| CN101921613A (en) * | 2009-06-17 | 2010-12-22 | 中国科学院大连化学物理研究所 | A kind of preparation method of ultra-low sulfur diesel oil |
| CN104229745A (en) * | 2014-09-01 | 2014-12-24 | 株洲起源科技有限责任公司 | Ultrasonic extraction method and process for processing slag containing elemental sulfur |
| US20150210949A1 (en) * | 2012-07-31 | 2015-07-30 | Cetamax Ventures Ltd. | Methods and Systems for Combined Oxidative and Hydrotreatment of Hydrocarbon Fuel |
| WO2019178701A1 (en) * | 2018-03-23 | 2019-09-26 | International Ultrasonic Technologies Inc. | Ultrasonic oxidative desulfurization of heavy fuel oils |
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| US20070051667A1 (en) * | 2005-09-08 | 2007-03-08 | Martinie Gary M | Diesel oil desulfurization by oxidation and extraction |
| US7744749B2 (en) | 2005-09-08 | 2010-06-29 | Saudi Arabian Oil Company | Diesel oil desulfurization by oxidation and extraction |
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| US8715489B2 (en) | 2005-09-08 | 2014-05-06 | Saudi Arabian Oil Company | Process for oxidative conversion of organosulfur compounds in liquid hydrocarbon mixtures |
| US9499751B2 (en) | 2005-09-08 | 2016-11-22 | Saudi Arabian Oil Company | Process for oxidative conversion of organosulfur compounds in liquid hydrocarbon mixtures |
| US20100140142A1 (en) * | 2008-12-10 | 2010-06-10 | Chevron U.S.A. Inc. | Removing unstable sulfur compounds from crude oil. |
| US9062260B2 (en) | 2008-12-10 | 2015-06-23 | Chevron U.S.A. Inc. | Removing unstable sulfur compounds from crude oil |
| US9499749B2 (en) | 2008-12-10 | 2016-11-22 | Chevron U.S.A. Inc. | Removing unstable sulfur compounds from crude oil |
| CN101921613A (en) * | 2009-06-17 | 2010-12-22 | 中国科学院大连化学物理研究所 | A kind of preparation method of ultra-low sulfur diesel oil |
| JP2015528847A (en) * | 2012-07-31 | 2015-10-01 | セタマックス ベンチャーズ リミテッド | Method and system for combined treatment of oxidation and hydrogenation of hydrocarbon fuel |
| US20150210949A1 (en) * | 2012-07-31 | 2015-07-30 | Cetamax Ventures Ltd. | Methods and Systems for Combined Oxidative and Hydrotreatment of Hydrocarbon Fuel |
| CN104229745A (en) * | 2014-09-01 | 2014-12-24 | 株洲起源科技有限责任公司 | Ultrasonic extraction method and process for processing slag containing elemental sulfur |
| WO2019178701A1 (en) * | 2018-03-23 | 2019-09-26 | International Ultrasonic Technologies Inc. | Ultrasonic oxidative desulfurization of heavy fuel oils |
| US11203724B2 (en) | 2018-03-23 | 2021-12-21 | International Ultrasonic Technologies Inc. | Ultrasonic oxidative desulfurization of heavy fuel oils |
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