GB512395A - A process for desulphurising mineral oils - Google Patents
A process for desulphurising mineral oilsInfo
- Publication number
- GB512395A GB512395A GB275939A GB275939A GB512395A GB 512395 A GB512395 A GB 512395A GB 275939 A GB275939 A GB 275939A GB 275939 A GB275939 A GB 275939A GB 512395 A GB512395 A GB 512395A
- Authority
- GB
- United Kingdom
- Prior art keywords
- sulphur
- extract
- rafflnate
- treated
- per cent
- Prior art date
- 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.)
- Expired
Links
- 239000002480 mineral oil Substances 0.000 title abstract 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical class [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 10
- 239000003921 oil Substances 0.000 abstract 7
- 239000002904 solvent Substances 0.000 abstract 7
- 239000005864 Sulphur Substances 0.000 abstract 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 4
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 abstract 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 3
- 239000003085 diluting agent Substances 0.000 abstract 3
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 abstract 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 150000007513 acids Chemical class 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 238000009835 boiling Methods 0.000 abstract 2
- 238000000605 extraction Methods 0.000 abstract 2
- 239000000446 fuel Substances 0.000 abstract 2
- 229930195733 hydrocarbon Natural products 0.000 abstract 2
- 150000002430 hydrocarbons Chemical class 0.000 abstract 2
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 235000010269 sulphur dioxide Nutrition 0.000 abstract 2
- 239000004291 sulphur dioxide Substances 0.000 abstract 2
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 abstract 1
- QKPVEISEHYYHRH-UHFFFAOYSA-N 2-methoxyacetonitrile Chemical compound COCC#N QKPVEISEHYYHRH-UHFFFAOYSA-N 0.000 abstract 1
- 239000004215 Carbon black (E152) Substances 0.000 abstract 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 abstract 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 abstract 1
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- -1 alkyl thiophenes Chemical class 0.000 abstract 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 abstract 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 239000004927 clay Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 abstract 1
- ZIUSEGSNTOUIPT-UHFFFAOYSA-N ethyl 2-cyanoacetate Chemical compound CCOC(=O)CC#N ZIUSEGSNTOUIPT-UHFFFAOYSA-N 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- CNUDBTRUORMMPA-UHFFFAOYSA-N formylthiophene Chemical compound O=CC1=CC=CS1 CNUDBTRUORMMPA-UHFFFAOYSA-N 0.000 abstract 1
- 239000007789 gas Substances 0.000 abstract 1
- 239000003502 gasoline Substances 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 239000003350 kerosene Substances 0.000 abstract 1
- VBEGHXKAFSLLGE-UHFFFAOYSA-N n-phenylnitramide Chemical compound [O-][N+](=O)NC1=CC=CC=C1 VBEGHXKAFSLLGE-UHFFFAOYSA-N 0.000 abstract 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 abstract 1
- RJQRCOMHVBLQIH-UHFFFAOYSA-N pentane-1-sulfonic acid Chemical class CCCCCS(O)(=O)=O RJQRCOMHVBLQIH-UHFFFAOYSA-N 0.000 abstract 1
- 239000003208 petroleum Substances 0.000 abstract 1
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 abstract 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- XTHPWXDJESJLNJ-UHFFFAOYSA-N sulfurochloridic acid Chemical class OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 abstract 1
- 150000003568 thioethers Chemical class 0.000 abstract 1
- 229930192474 thiophene Natural products 0.000 abstract 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
- C10G21/00—Refining of hydrocarbon oils, in the absence of hydrogen, by extraction with selective solvents
- C10G21/06—Refining of hydrocarbon oils, in the absence of hydrogen, by extraction with selective solvents characterised by the solvent used
- C10G21/12—Organic compounds only
- C10G21/22—Compounds containing sulfur, selenium, or tellurium
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)
Abstract
512,395. Desulphurizing oils motor fuels. NAAMLOOZE VENNOOTSCHAP DE BATAAFSCHE PETROLEUM MAATSCHAPPIJ, and FIFE, J. G. Aug. 11, 1938, No. 2759/39. Divided out of and addition to 512,364. [Class 91] Low boiling mineral oils are freed from sulphur compounds, such as mercaptans, thioethers and alkyl thiophenes, without affecting aromatic hydrocarbons or mono-olefines, by extracting the oil with a selective solvent for sulphur compounds, separating the extract and treating it at a temperature not above 40‹C., with an aliphatic sulphonic acid, whereupon a further rafflnate and extract are formed and separated. The final raffinate free from sulphur compounds is combined with the first rafflnate to form a motor fuel. Naphtha, gasoline, kerosene, gas oil, from straight-run, cracked, or polymerized oils may be treated. Selective solvents specified are, sulphur dioxide and acetone, thiophene aldehyde, methyl or ethyl cyanide, ethyl cyanoacetate, nitroaniline, aniline, ethylene diamine, methoxy methyl cyanide, and methyl carbitol. Sulphonic acids specified are, methyl, ethyl, propyl, isopropyl, butyl, and amyl sulphonic acids, or the corresponding chlorsulphonic acids, used alone or diluted with a polar diluent, such as one of the selective solvents, alcohol, acetone, or water, or a hydrocarbon diluent, such as Edeleanu extract. Such diluted sulphonic acids are used with oils containing large amounts of olefines. Oil is introduced into an extraction zone B to which a selective solvent and an auxiliary solvent such as naphtha flow in countercurrent. The rafflnate containing paraffins, naphthenes and mono-olefines, passes to a separator 33 and then tank 34, and the extract containing aromatic, unsaturated, and sulphur compounds, passes to a still 32. The. solvent-free extract passes to a second countercurrent extraction zone A, which may be a packed tower, or mixers and settlers, where it is treated with the sulphonic acid and a light naphtha or white oil, as diluent. The extract free from hydrocarbons, passes to a settler 9 in admixture with water or alcohol which dissolves the sulphur compounds, leaving a sulphonic acid layer which passes to a vacuum still 11. The alcohol and auxiliary solvent are recovered from the extract in a still 14. The sulphur-free rafflnate consisting of aromatic and unsaturated compounds and auxiliary solvent is washed with water in a separator 19, distilled with steam at 21, and, if desired, finally treated with clay. This is then united with the first raffinate. In an example, 100 parts of cracked distillate boiling at 150-200‹C. containing 1.1 per cent. sulphur is treated with sulphur dioxide and octane, yielding 20 parts of extract containing 4.4 per cent. of sulphur. The extract is treated with methyl sulphonic acid and isopentane, yielding 12.2 parts of rafflnate containing 1.2 per cent. of sulphur, and an extract containing 14 per cent. of sulphur. The combined rafflnates form 92 parts containing .3 per cent. of sulphur.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB275939A GB512395A (en) | 1938-08-11 | 1938-08-11 | A process for desulphurising mineral oils |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB275939A GB512395A (en) | 1938-08-11 | 1938-08-11 | A process for desulphurising mineral oils |
Publications (1)
Publication Number | Publication Date |
---|---|
GB512395A true GB512395A (en) | 1939-09-01 |
Family
ID=9745349
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB275939A Expired GB512395A (en) | 1938-08-11 | 1938-08-11 | A process for desulphurising mineral oils |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB512395A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2602770A (en) * | 1950-05-23 | 1952-07-08 | Standard Oil Co | Process for desulfurizing hydrocarbons using a mixture of boron trifluoride and an alkane sulfonic acid as reagent |
CN115400448A (en) * | 2022-08-30 | 2022-11-29 | 华东理工大学 | Application of No. 5 industrial white oil as MTBE (methyl tert-butyl ether) extraction anti-coking agent and MTBE desulfurization method |
-
1938
- 1938-08-11 GB GB275939A patent/GB512395A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2602770A (en) * | 1950-05-23 | 1952-07-08 | Standard Oil Co | Process for desulfurizing hydrocarbons using a mixture of boron trifluoride and an alkane sulfonic acid as reagent |
CN115400448A (en) * | 2022-08-30 | 2022-11-29 | 华东理工大学 | Application of No. 5 industrial white oil as MTBE (methyl tert-butyl ether) extraction anti-coking agent and MTBE desulfurization method |
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