CA2744257A1 - Methode de desulfuration oxydative avec melange pour du carburant diesel et dispositf a cet effet - Google Patents

Methode de desulfuration oxydative avec melange pour du carburant diesel et dispositf a cet effet Download PDF

Info

Publication number: CA2744257A1
Authority: CA; Canada
Prior art keywords: phase; mixing; accordance; solution; fossil fuel
Prior art date: 2010-07-20
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Abandoned

Application number

CA2744257A

Other languages

English (en)

Inventor

Hsin Tung Lin

Meng-Wei Wan

Ming-Chun Lu

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Individual

Original Assignee

Individual

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2010-07-20

Filing date

2011-06-23

Publication date

2012-01-20

2011-06-23 Application filed by Individual filed Critical Individual

2012-01-20 Publication of CA2744257A1 publication Critical patent/CA2744257A1/fr

Status Abandoned legal-status Critical Current

Links

238000002156 mixing Methods 0.000 title claims abstract description 54
238000006477 desulfuration reaction Methods 0.000 title claims abstract description 47
230000023556 desulfurization Effects 0.000 title claims abstract description 47
238000000034 method Methods 0.000 title claims abstract description 35
239000002283 diesel fuel Substances 0.000 title abstract description 19
230000001590 oxidative effect Effects 0.000 title abstract description 14
239000002803 fossil fuel Substances 0.000 claims abstract description 30
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims abstract description 28
150000003457 sulfones Chemical class 0.000 claims abstract description 25
239000003444 phase transfer catalyst Substances 0.000 claims abstract description 20
CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 claims abstract description 17
WFIYFFUAOQKJJS-UHFFFAOYSA-N tetraoctylphosphanium Chemical class CCCCCCCC[P+](CCCCCCCC)(CCCCCCCC)CCCCCCCC WFIYFFUAOQKJJS-UHFFFAOYSA-N 0.000 claims abstract description 8
239000003054 catalyst Substances 0.000 claims description 31
239000007800 oxidant agent Substances 0.000 claims description 24
239000012071 phase Substances 0.000 claims description 23
150000003568 thioethers Chemical class 0.000 claims description 21
229910052751 metal Inorganic materials 0.000 claims description 19
239000002184 metal Substances 0.000 claims description 19
239000007788 liquid Substances 0.000 claims description 14
230000015572 biosynthetic process Effects 0.000 claims description 11
238000005755 formation reaction Methods 0.000 claims description 11
239000012074 organic phase Substances 0.000 claims description 11
238000007254 oxidation reaction Methods 0.000 claims description 10
239000008346 aqueous phase Substances 0.000 claims description 9
239000002798 polar solvent Substances 0.000 claims description 9
239000012429 reaction media Substances 0.000 claims description 9
230000003647 oxidation Effects 0.000 claims description 8
125000001424 substituent group Chemical group 0.000 claims description 7
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 6
125000004432 carbon atom Chemical group C* 0.000 claims description 6
125000000217 alkyl group Chemical group 0.000 claims description 5
JTJMJGYZQZDUJJ-UHFFFAOYSA-N phencyclidine Chemical class C1CCCCN1C1(C=2C=CC=CC=2)CCCCC1 JTJMJGYZQZDUJJ-UHFFFAOYSA-N 0.000 claims description 5
150000003242 quaternary ammonium salts Chemical group 0.000 claims description 5
238000004821 distillation Methods 0.000 claims description 4
JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 claims description 3
CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 claims description 3
229910052742 iron Inorganic materials 0.000 claims description 3
IYDGMDWEHDFVQI-UHFFFAOYSA-N phosphoric acid;trioxotungsten Chemical group O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.OP(O)(O)=O IYDGMDWEHDFVQI-UHFFFAOYSA-N 0.000 claims description 3
238000004064 recycling Methods 0.000 claims description 3
VMQMZMRVKUZKQL-UHFFFAOYSA-N Cu+ Chemical compound [Cu+] VMQMZMRVKUZKQL-UHFFFAOYSA-N 0.000 claims description 2
238000013019 agitation Methods 0.000 claims description 2
125000003710 aryl alkyl group Chemical group 0.000 claims description 2
125000003118 aryl group Chemical group 0.000 claims description 2
BFGKITSFLPAWGI-UHFFFAOYSA-N chromium(3+) Chemical compound [Cr+3] BFGKITSFLPAWGI-UHFFFAOYSA-N 0.000 claims description 2
JOPOVCBBYLSVDA-UHFFFAOYSA-N chromium(6+) Chemical class [Cr+6] JOPOVCBBYLSVDA-UHFFFAOYSA-N 0.000 claims description 2
239000003125 aqueous solvent Substances 0.000 claims 3
LSGOVYNHVSXFFJ-UHFFFAOYSA-N vanadate(3-) Chemical class [O-][V]([O-])([O-])=O LSGOVYNHVSXFFJ-UHFFFAOYSA-N 0.000 claims 1
229910052717 sulfur Inorganic materials 0.000 abstract description 23
239000011593 sulfur Substances 0.000 abstract description 23
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract description 22
239000000446 fuel Substances 0.000 abstract description 12
239000000203 mixture Substances 0.000 abstract description 11
229930195733 hydrocarbon Natural products 0.000 abstract description 6
150000002430 hydrocarbons Chemical class 0.000 abstract description 6
150000003464 sulfur compounds Chemical class 0.000 abstract description 6
239000003502 gasoline Substances 0.000 abstract description 5
150000001875 compounds Chemical class 0.000 abstract description 4
239000003209 petroleum derivative Substances 0.000 abstract description 3
230000036541 health Effects 0.000 abstract description 2
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 21
239000000243 solution Substances 0.000 description 21
230000008569 process Effects 0.000 description 17
238000006243 chemical reaction Methods 0.000 description 10
239000000839 emulsion Substances 0.000 description 10
239000003921 oil Substances 0.000 description 9
239000007864 aqueous solution Substances 0.000 description 8
239000006227 byproduct Substances 0.000 description 7
239000012530 fluid Substances 0.000 description 6
150000002432 hydroperoxides Chemical class 0.000 description 5
150000003462 sulfoxides Chemical class 0.000 description 5
238000002604 ultrasonography Methods 0.000 description 5
238000010586 diagram Methods 0.000 description 4
239000003208 petroleum Substances 0.000 description 4
239000000047 product Substances 0.000 description 4
230000009467 reduction Effects 0.000 description 4
239000002904 solvent Substances 0.000 description 4
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 3
239000002253 acid Substances 0.000 description 3
239000007789 gas Substances 0.000 description 3
229910000037 hydrogen sulfide Inorganic materials 0.000 description 3
238000004519 manufacturing process Methods 0.000 description 3
239000011541 reaction mixture Substances 0.000 description 3
238000013341 scale-up Methods 0.000 description 3
238000001179 sorption measurement Methods 0.000 description 3
229910052723 transition metal Inorganic materials 0.000 description 3
150000003624 transition metals Chemical class 0.000 description 3
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
230000004913 activation Effects 0.000 description 2
238000009835 boiling Methods 0.000 description 2
238000002485 combustion reaction Methods 0.000 description 2
238000005336 cracking Methods 0.000 description 2
230000000694 effects Effects 0.000 description 2
238000005516 engineering process Methods 0.000 description 2
230000007613 environmental effect Effects 0.000 description 2
238000000605 extraction Methods 0.000 description 2
-1 ferrous salts Chemical class 0.000 description 2
229910052739 hydrogen Inorganic materials 0.000 description 2
239000001257 hydrogen Substances 0.000 description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
125000001905 inorganic group Chemical group 0.000 description 2
230000007774 longterm Effects 0.000 description 2
125000000962 organic group Chemical group 0.000 description 2
238000012545 processing Methods 0.000 description 2
238000011084 recovery Methods 0.000 description 2
230000001105 regulatory effect Effects 0.000 description 2
239000007787 solid Substances 0.000 description 2
CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 2
238000012546 transfer Methods 0.000 description 2
WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 2
229910052721 tungsten Inorganic materials 0.000 description 2
239000010937 tungsten Substances 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
AKUNSTOMHUXJOZ-UHFFFAOYSA-N 1-hydroperoxybutane Chemical compound CCCCOO AKUNSTOMHUXJOZ-UHFFFAOYSA-N 0.000 description 1
UBCLHQOSNQCIHZ-UHFFFAOYSA-N 2,3-dibenzylthiophene Chemical compound C=1C=CC=CC=1CC=1C=CSC=1CC1=CC=CC=C1 UBCLHQOSNQCIHZ-UHFFFAOYSA-N 0.000 description 1
PSBSELFEZHDPTA-UHFFFAOYSA-N 2-hydroperoxy-2-methoxypropane Chemical compound COC(C)(C)OO PSBSELFEZHDPTA-UHFFFAOYSA-N 0.000 description 1
XRXANEMIFVRKLN-UHFFFAOYSA-N 2-hydroperoxy-2-methylbutane Chemical compound CCC(C)(C)OO XRXANEMIFVRKLN-UHFFFAOYSA-N 0.000 description 1
SPQMVUPFYWDFCB-UHFFFAOYSA-N 2-hydroperoxybutane Chemical compound CCC(C)OO SPQMVUPFYWDFCB-UHFFFAOYSA-N 0.000 description 1
SGJUFIMCHSLMRJ-UHFFFAOYSA-N 2-hydroperoxypropane Chemical compound CC(C)OO SGJUFIMCHSLMRJ-UHFFFAOYSA-N 0.000 description 1
ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
230000007059 acute toxicity Effects 0.000 description 1
231100000403 acute toxicity Toxicity 0.000 description 1
238000003915 air pollution Methods 0.000 description 1
150000001335 aliphatic alkanes Chemical class 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
125000000129 anionic group Chemical group 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
238000010923 batch production Methods 0.000 description 1
125000001246 bromo group Chemical group Br* 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
238000001311 chemical methods and process Methods 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000003245 coal Substances 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
239000002826 coolant Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
239000010779 crude oil Substances 0.000 description 1
150000001924 cycloalkanes Chemical class 0.000 description 1
230000034994 death Effects 0.000 description 1
231100000517 death Toxicity 0.000 description 1
238000013461 design Methods 0.000 description 1
LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
ONYODNNNQUGXKN-UHFFFAOYSA-N dioxido(dioxo)chromium;tetraoctylphosphanium Chemical compound [O-][Cr]([O-])(=O)=O.CCCCCCCC[P+](CCCCCCCC)(CCCCCCCC)CCCCCCCC.CCCCCCCC[P+](CCCCCCCC)(CCCCCCCC)CCCCCCCC ONYODNNNQUGXKN-UHFFFAOYSA-N 0.000 description 1
238000009826 distribution Methods 0.000 description 1
238000005265 energy consumption Methods 0.000 description 1
239000000295 fuel oil Substances 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
230000005484 gravity Effects 0.000 description 1
231100001261 hazardous Toxicity 0.000 description 1
239000000383 hazardous chemical Substances 0.000 description 1
231100000206 health hazard Toxicity 0.000 description 1
239000010763 heavy fuel oil Substances 0.000 description 1
FGGJBCRKSVGDPO-UHFFFAOYSA-N hydroperoxycyclohexane Chemical compound OOC1CCCCC1 FGGJBCRKSVGDPO-UHFFFAOYSA-N 0.000 description 1
ILHIHKRJJMKBEE-UHFFFAOYSA-N hydroperoxyethane Chemical compound CCOO ILHIHKRJJMKBEE-UHFFFAOYSA-N 0.000 description 1
MEUKEBNAABNAEX-UHFFFAOYSA-N hydroperoxymethane Chemical compound COO MEUKEBNAABNAEX-UHFFFAOYSA-N 0.000 description 1
TUJKJAMUKRIRHC-UHFFFAOYSA-N hydroxyl Chemical compound [OH] TUJKJAMUKRIRHC-UHFFFAOYSA-N 0.000 description 1
238000012423 maintenance Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
230000007246 mechanism Effects 0.000 description 1
229910021645 metal ion Inorganic materials 0.000 description 1
230000004048 modification Effects 0.000 description 1
238000012986 modification Methods 0.000 description 1
229910052750 molybdenum Inorganic materials 0.000 description 1
239000011733 molybdenum Substances 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
150000002898 organic sulfur compounds Chemical class 0.000 description 1
239000013618 particulate matter Substances 0.000 description 1
MPNNOLHYOHFJKL-UHFFFAOYSA-N peroxyphosphoric acid Chemical compound OOP(O)(O)=O MPNNOLHYOHFJKL-UHFFFAOYSA-N 0.000 description 1
238000005191 phase separation Methods 0.000 description 1
231100000572 poisoning Toxicity 0.000 description 1
230000000607 poisoning effect Effects 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
230000005180 public health Effects 0.000 description 1
125000001453 quaternary ammonium group Chemical group 0.000 description 1
239000000376 reactant Substances 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
238000007670 refining Methods 0.000 description 1
239000002760 rocket fuel Substances 0.000 description 1
239000000523 sample Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000011877 solvent mixture Substances 0.000 description 1
150000003463 sulfur Chemical class 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
NCYWEOAYLCHMDJ-UHFFFAOYSA-M tetraoctylphosphanium;acetate Chemical compound CC([O-])=O.CCCCCCCC[P+](CCCCCCCC)(CCCCCCCC)CCCCCCCC NCYWEOAYLCHMDJ-UHFFFAOYSA-M 0.000 description 1
QVBRLOSUBRKEJW-UHFFFAOYSA-M tetraoctylphosphanium;bromide Chemical compound [Br-].CCCCCCCC[P+](CCCCCCCC)(CCCCCCCC)CCCCCCCC QVBRLOSUBRKEJW-UHFFFAOYSA-M 0.000 description 1
AXTXARBFPWQUQA-UHFFFAOYSA-M tetraoctylphosphanium;chloride Chemical compound [Cl-].CCCCCCCC[P+](CCCCCCCC)(CCCCCCCC)CCCCCCCC AXTXARBFPWQUQA-UHFFFAOYSA-M 0.000 description 1
JTFPRVNRGNKAAV-UHFFFAOYSA-M tetraoctylphosphanium;iodide Chemical compound [I-].CCCCCCCC[P+](CCCCCCCC)(CCCCCCCC)CCCCCCCC JTFPRVNRGNKAAV-UHFFFAOYSA-M 0.000 description 1
CMPGARWFYBADJI-UHFFFAOYSA-L tungstic acid Chemical compound O[W](O)(=O)=O CMPGARWFYBADJI-UHFFFAOYSA-L 0.000 description 1
229910001456 vanadium ion Inorganic materials 0.000 description 1

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
- 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
- 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
- C10G21/00—Refining of hydrocarbon oils, in the absence of hydrogen, by extraction with selective solvents
- 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
- C10G21/00—Refining of hydrocarbon oils, in the absence of hydrogen, by extraction with selective solvents
- C10G21/28—Recovery of used solvent
- 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
- 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
- C10G27/14—Refining of hydrocarbon oils in the absence of hydrogen, by oxidation with oxygen or compounds generating oxygen with ozone-containing gases
- 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
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/10—Feedstock materials
- C10G2300/1037—Hydrocarbon fractions
- C10G2300/1048—Middle distillates
- C10G2300/1055—Diesel having a boiling range of about 230 - 330 °C
- 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
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/20—Characteristics of the feedstock or the products
- C10G2300/201—Impurities
- C10G2300/202—Heteroatoms content, i.e. S, N, O, P
- 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
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/40—Characteristics of the process deviating from typical ways of processing
- C10G2300/4081—Recycling aspects
- 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
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/40—Characteristics of the process deviating from typical ways of processing
- C10G2300/44—Solvents

Landscapes

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)

CA2744257A 2010-07-20 2011-06-23 Methode de desulfuration oxydative avec melange pour du carburant diesel et dispositf a cet effet Abandoned CA2744257A1 (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US12/840,259 US20120018350A1 (en)	2010-07-20	2010-07-20	Mixing-assisted oxidative desulfurization of diesel fuel using quaternary ammonium salt and portable unit thereof
US12/840,259		2010-07-20

Publications (1)

Publication Number	Publication Date
CA2744257A1 true CA2744257A1 (fr)	2012-01-20

Family

ID=44496518

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA2744257A Abandoned CA2744257A1 (fr)	2010-07-20	2011-06-23	Methode de desulfuration oxydative avec melange pour du carburant diesel et dispositf a cet effet

Country Status (6)

Country	Link
US (1)	US20120018350A1 (fr)
EP (1)	EP2410038A3 (fr)
JP (1)	JP2012025933A (fr)
CN (2)	CN102337149A (fr)
CA (1)	CA2744257A1 (fr)
TW (1)	TWI417375B (fr)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
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2010
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- 2010-10-28 TW TW099136872A patent/TWI417375B/zh not_active IP Right Cessation
- 2010-12-23 CN CN2010106010846A patent/CN102337149A/zh active Pending
- 2010-12-23 CN CN2010206753740U patent/CN201952397U/zh not_active Expired - Fee Related
2011
- 2011-04-08 EP EP11161598A patent/EP2410038A3/fr not_active Ceased
- 2011-04-25 JP JP2011097457A patent/JP2012025933A/ja active Pending
- 2011-06-23 CA CA2744257A patent/CA2744257A1/fr not_active Abandoned

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Publication number	Publication date
EP2410038A2 (fr)	2012-01-25
EP2410038A3 (fr)	2012-05-23
US20120018350A1 (en)	2012-01-26
CN102337149A (zh)	2012-02-01
TWI417375B (zh)	2013-12-01
CN201952397U (zh)	2011-08-31
TW201204825A (en)	2012-02-01
JP2012025933A (ja)	2012-02-09

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Publication	Publication Date	Title
EP2410038A2 (fr)	2012-01-25	Procédé de désulfurisation oxydative assisté par mélange de carburant diesel et dispositif associé
US8197763B2 (en)	2012-06-12	Ultrasound-assisted oxidative desulfurization of diesel fuel using quaternary ammonium fluoride and portable unit for ultrasound-assisted oxidative desulfurization
KR101432857B1 (ko)	2014-08-26	석유의 산화적 탈황반응 및 탈질소반응
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EP3441442B1 (fr)	2022-02-02	Procédé de réduction de la teneur en soufre de carburants
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CA2422866C (fr)	2008-05-20	Desulfuration oxydante de combustibles fossiles par ultrasons
JP5444402B2 (ja)	2014-03-19	改良された分離方法
Gao et al.	2006	Deep desulfurization from fuel oil via selective oxidation using an amphiphilic peroxotungsten catalyst assembled in emulsion droplets
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JP5838211B2 (ja)	2016-01-06	酸化した炭化水素燃料からのスルホンの除去
Cheng	2008	Ultra clean fuels via modified UAOD process with room temperature ionic liquid (RTIL) & solid catalyst polishing
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CA2543367A1 (fr)	2005-05-06	Procede et appareil permettant de convertir et d'oter de l'organo-sulfure et d'autres composes oxydables a partir de carburants distilles et compositions ainsi obtenues
EP0956124A1 (fr)	1999-11-17	Procede d'extraction
Wan	2006	Development of a portable, modular unit for the optimization of ultrasound-assisted oxidative desulfurization of diesel
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WO2024095167A1 (fr)	2024-05-10	Désulfuration oxydative de mazout assistée par ultrasons faisant appel à des catalyseurs à base d'oxydes métalliques
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Campos Martín et al.	2010	Oxidative processes of desulfurization of liquid
HK1182733B (en)	2015-10-23	Sulfone removal from an oxidized hydrocarbon fuel