GB680655A - Improvements in or relating to the purification of kerosene - Google Patents

Improvements in or relating to the purification of kerosene

Info

Publication number
GB680655A
GB680655A GB4848/50A GB484850A GB680655A GB 680655 A GB680655 A GB 680655A GB 4848/50 A GB4848/50 A GB 4848/50A GB 484850 A GB484850 A GB 484850A GB 680655 A GB680655 A GB 680655A
Authority
GB
United Kingdom
Prior art keywords
sulphur dioxide
raffinate
adsorbent
kerosene
per
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
Application number
GB4848/50A
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.)
Standard Oil Development Co
Original Assignee
Standard Oil Development Co
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.)
Filing date
Publication date
Application filed by Standard Oil Development Co filed Critical Standard Oil Development Co
Publication of GB680655A publication Critical patent/GB680655A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING 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
    • C10G21/00Refining of hydrocarbon oils, in the absence of hydrogen, by extraction with selective solvents
    • C10G21/06Refining of hydrocarbon oils, in the absence of hydrogen, by extraction with selective solvents characterised by the solvent used
    • C10G21/08Inorganic compounds only
    • C10G21/10Sulfur dioxide

Landscapes

  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Inorganic Chemistry (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)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)

Abstract

<PICT:0680655/III/1> Kerosene is initially treated with sulphur dioxide to form a raffinate and extract, and the raffinate thus obtained is treated with bauxite or absorbent clay. The pocess is particularly applicable to those kerosenes having a wick char value of more than 10 as measured by test method 10-44 of the Institute of Petroleum, and to those obtained by the fractionation of crude oil having a sulphur content of 1.4 per cent or more. The sulphur dioxide treatment is preferably carried out in counter-current in the liquid phase at a temperature between -40 and +25 DEG F and 0-100 pounds per square inch. The amount of sulphur dioxide is preferably 25-100 per cent of the oil used. The solid adsorbent may be formed into a bed through which the raffinate is passed, or it may be formed into a slurry with the raffinate. O.1 to 4 lbs. adsorbent per U.S. barrel of oil (preferably 1 lb. per U.S. barrel) may be employed at a feed rate of about 0.25 to 4 vols. of oil per volume of adsorbent per hour. The adsorbent step is usually carried out at atmospheric temperature and pressure, but elevated temperature and pressure may be used if desired. Other additional steps, e.g. hypochlorite sweetening or Doctor sweetening, may be employed to reduce the sulphur content further. In the preferred embodiment the sulphur dioxide treatment is followed by a process for the removal of mercaptans and then the kerosene is treated with the adsorbent. As shown, kerosene is contacted in zone 1 with sulphur dioxide in counter-current, the sulphur dioxide flowing downwardly. The extract phase may be distilled to recover sulphur dioxide, which may be recycled. The raffinate is distilled in zone 8, the sulphur dioxide being removed and recycled through line 9, the raffinate product being passed through line 10 to zone 11 for hypochlorite sweetening. The hypochorite solution (2-30g/ litre of NaOCl and containing more than 2g/ litre of free NaOH) in an amount equivalent to 1-10 volume per cent, is mixed with the raffinate product in an orifice mixer 25 and allowed to settle in vessel 11. The sweetened kerosene is removed through line 12 and treated with sand or other moisture removing agent in vessel 13, the dried kerosene passing through line 15 to the adsorbent treating tower 16 filled with bauxite or an adsorbent clay such as Fuller's earth. In an example (4) a kerosene of boiling range 357-512 DEG F from an Iraq crude oil and having a wick char value of 46 is treated with sulphur dioxide and subsequently with Attapulgus clay, the product having a wick char value of 6.
GB4848/50A 1949-05-26 1950-02-24 Improvements in or relating to the purification of kerosene Expired GB680655A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US680655XA 1949-05-26 1949-05-26

Publications (1)

Publication Number Publication Date
GB680655A true GB680655A (en) 1952-10-08

Family

ID=22080199

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4848/50A Expired GB680655A (en) 1949-05-26 1950-02-24 Improvements in or relating to the purification of kerosene

Country Status (1)

Country Link
GB (1) GB680655A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4948494A (en) * 1989-06-28 1990-08-14 Union Oil Company Of California Removal of hydrogen sulfide from produced fluids
US5346614A (en) * 1992-11-10 1994-09-13 Union Oil Company Of California Removal of hydrogen sulfide from an oil-containing mixture having a continuous aqueous phase

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4948494A (en) * 1989-06-28 1990-08-14 Union Oil Company Of California Removal of hydrogen sulfide from produced fluids
US5346614A (en) * 1992-11-10 1994-09-13 Union Oil Company Of California Removal of hydrogen sulfide from an oil-containing mixture having a continuous aqueous phase

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