GB667368A - Process for the removal of aromatic mercaptans from catalytically cracked gasoline - Google Patents

Process for the removal of aromatic mercaptans from catalytically cracked gasoline

Info

Publication number
GB667368A
GB667368A GB19811/48A GB1981148A GB667368A GB 667368 A GB667368 A GB 667368A GB 19811/48 A GB19811/48 A GB 19811/48A GB 1981148 A GB1981148 A GB 1981148A GB 667368 A GB667368 A GB 667368A
Authority
GB
United Kingdom
Prior art keywords
gasoline
solution
acidification
thiophenol
mercaptans
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
GB19811/48A
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 GB667368A publication Critical patent/GB667368A/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
    • C10G19/00Refining hydrocarbon oils in the absence of hydrogen, by alkaline treatment

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

The spent aqueous alkali metal hydroxide, which results from the refining of catalytically cracked gasoline distillates in the absence of oxygen (see Group III), is acidified with a mineral acid such as hydrochloric acid to liberate the impurities, particularly aromatic mercaptans, removed from the gasoline. Aliphatic mercaptans and phenols are substantially completely released from the hydroxide solution on acidification to a pH of approximately 9, and separate as an oily layer which may be withdrawn. On further acidification of the hydroxide solution to approximately pH 2, the aromatic mercaptans are substantially completely released and also separate as an oily layer which may be withdrawn. Some olefins may be present in the hydroxide solution, so that it is desirable to exclued oxygen during the acidification. According to an alternative method, the hydroxide solution be acidified in one stage to a pH of about 2, another extracted with a solvent such as ether, oxygen during the acidification. According to an alternative method, the hydroxide solution may be acidified in one stage to a pH of about 2, another extracted with a solvent such as ether, benzene, pentane or hexane. The extract is freed from solvent and treated with alkali hydroxide solution. There is thus obtained a solution of aromatic mercaptans, aliphatic mercaptans and phenols, free of any residual oil. This new hydroxide solution is then partially acidified to remove the aliphatic mercaptans and phenols. In the examples: (1) a spent caustic soda solution from the gaoline refining is acidified with hydrochloric acid to pH 6 and extracted with ether; the extract after evaporation of the solvent is mixed with caustic soda solution and the new caustic solution is then acidified, first to pH 11, then to pH 9, and finally to pH 2; at each acidification an oily layer separates and is removed, that removed on acidification to pH 2 being the aromatic mercaptan fraction composed mainly of thiophenol; (2) a spent caustic soda solution from the gasoline refining is acidified with hydrochloric acid, first to pH 9 and then to pH 2; at each acidification an oily layer separates and is removed, that removed on acidification to pH 2 consisting principally of thiocresols. The aromatic mercaptans which may be present in the gasoline are thiophenol, methyl thiophenol, dimethyl thiophenol, ethyl thiophenol, diethyl thiophenol, propyl thiophenol, and dipropyl thiophenol.ALSO:A gasoline distillate containing aromatic mercaptans is prepared by a catalytic cracking process and is maintained out of contact with oxygen until after it has been sweetened by contact with an aqueous solution of an alkali metal hydroxide. The aqueous alkali solution removes the aromatic mercaptans and in this way excessive gum formation in the gasoline is avoided, since it is stated that, in the presence of oxygen, the aromatic mercaptons catalyze the oxidation of olefins and diolefins p present in the gasoline. The olefins and diolefins, in such circumstances, are oxdized to peroxides, and these in turn react with the aromatic mercaptons with the formation of gum. In an example, a West Texas gas oil boiling in the range of about 400 DEG -700 DEG F. is cracked at 900 DEG -1000 DEG F. and 5-25 p.s.i. pressure in the presence of a fluidized silica-alumina gel catalyst containing approximately 15 per cent silica. A gasoline fraction having an end point of about 400 DEG F. is distilled from the cracked products and, before this gasoline comes into contact with oxygen, it is washed with aqueous caustic soda. The caustic soda solution may have been freed of oxygen before use by purging with an intert gas. The treatment with caustic soda solution may take place in an inert atmosphere, and any phenols or aliphatic mercaptans present will also be removed by the caustic treatment. The Specification as open to inspection under Sect. 91 refers to the sweetening, in the absence of oxygen, according to the process, of any gasoline prepared by a cracking process. This subject-matter does not appear in the Specification as accepted.
GB19811/48A 1947-09-17 1948-07-23 Process for the removal of aromatic mercaptans from catalytically cracked gasoline Expired GB667368A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US667368XA 1947-09-17 1947-09-17

Publications (1)

Publication Number Publication Date
GB667368A true GB667368A (en) 1952-02-27

Family

ID=22071361

Family Applications (1)

Application Number Title Priority Date Filing Date
GB19811/48A Expired GB667368A (en) 1947-09-17 1948-07-23 Process for the removal of aromatic mercaptans from catalytically cracked gasoline

Country Status (1)

Country Link
GB (1) GB667368A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1027352B (en) * 1952-11-20 1958-04-03 Exxon Research Engineering Co Process for the desulphurisation of hydrocarbons from the boiling range of motor fuels and distillate heating oil

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1027352B (en) * 1952-11-20 1958-04-03 Exxon Research Engineering Co Process for the desulphurisation of hydrocarbons from the boiling range of motor fuels and distillate heating oil

Similar Documents

Publication Publication Date Title
US9458392B2 (en) Hydrocarbon treatment process
US3413307A (en) Desulfurization process
US2472473A (en) Conversion of hydrosulfides to neutral sulfur substances
US2862804A (en) Process for sweetening and stabilizing hydrocarbons with an organic epoxide and an aqueous alkaline phenol
US2740749A (en) Regeneration of aqueous caustic-mercaptide solutions with oxygen and a liquid hydrocarbon
GB667368A (en) Process for the removal of aromatic mercaptans from catalytically cracked gasoline
US2347515A (en) Refining mineral oils
US2084575A (en) Process of refining gasoline containing mercaptans
US2163227A (en) Process for desulphurizing alkyl phenols
US2719109A (en) Regeneration of aqueous alkaline solutions
US2301270A (en) Process for the production of petroleum phenols
US2727850A (en) Sweetening process
US2645602A (en) Sweetening hydrocarbon distillates
US2202039A (en) Process for the removal of mercaptans from hydrocarbon distillates
US3049414A (en) Color-stable gasoline
US2346497A (en) Solutizer process
JPH0649872B2 (en) How to improve the cetane number of straight-run gas oil
US2320939A (en) Removal of mercaptans from mercaptan-solvent mixtures
US2949421A (en) Preparation and use of acid activated clay
US2051612A (en) Method of treating oils
US2043254A (en) Treatment of hydrocarbon oil
US3398086A (en) Process for treating hydrocarbon distillates containing mercaptan and color-forming components
US2729591A (en) Sweetening of petroleum oils containing mercaptans with alkali and oxygen and then with alkali, a solutizer and oxygen
US2036396A (en) Treatment of mineral oils
US2846357A (en) Refining of light and heavy petroleum hydrocarbons separately with alkali and cresylic acid followed by regeneration of the alkali solution