GB479345A - Improvements relating to the production of motor fuel - Google Patents

Improvements relating to the production of motor fuel

Info

Publication number
GB479345A
GB479345A GB2101136A GB2101136A GB479345A GB 479345 A GB479345 A GB 479345A GB 2101136 A GB2101136 A GB 2101136A GB 2101136 A GB2101136 A GB 2101136A GB 479345 A GB479345 A GB 479345A
Authority
GB
United Kingdom
Prior art keywords
iso
butane
butene
paraffin
diisobutene
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
GB2101136A
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.)
Anglo Iranian Oil Co Ltd
Original Assignee
Anglo Iranian Oil Co Ltd
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 Anglo Iranian Oil Co Ltd filed Critical Anglo Iranian Oil Co Ltd
Priority to GB2101136A priority Critical patent/GB479345A/en
Publication of GB479345A publication Critical patent/GB479345A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2/00Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
    • C07C2/54Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition of unsaturated hydrocarbons to saturated hydrocarbons or to hydrocarbons containing a six-membered aromatic ring with no unsaturation outside the aromatic ring
    • C07C2/56Addition to acyclic hydrocarbons
    • C07C2/58Catalytic processes
    • C07C2/62Catalytic processes with acids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2527/00Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • C07C2527/02Sulfur, selenium or tellurium; Compounds thereof
    • C07C2527/053Sulfates or other compounds comprising the anion (SnO3n+1)2-
    • C07C2527/054Sulfuric acid or other acids with the formula H2Sn03n+1

Abstract

An aviation or motor spirit or constituent thereof is obtained by the alkylation of an isoparaffin. Iso-butane or iso-pentane is condensed with an olefine or olefines, e.g. propylene, iso- or n-butene or the lower polymerides thereof, particularly the dimeride and trimeride, in the presence of sulphuric acid at low temperatures, e.g. -10 to + 30 DEG C. and in substantially equimolecular proportions. On settlement, an upper hydrocarbon layer separates, from which the spirit may be produced by distillation. Normal paraffins or inert hydrocarbons may be present, but preferably aromatic hydrocarbons are absent. An excess of the iso-paraffin may be used, and this is stated to increase the yield of the condensate. The reaction is carried out in the liquid phase and if necessary, pressure sufficient to maintain the liquid phase may be used. The iso-paraffin may be mixed with the acid, and the olefine added gradually with vigorous stirring, which may be maintained after all the reactants are mixed. Examples describe products obtained from iso-butane and diisobutene; iso-pentane and diisobutene; isobutane and a polymer gasoline produced by the catalytic polymerization of olefines; isobutane and iso-butene, alone or mixed with diisobutene or triisobutene; iso-butane and propylene; iso-butane and butene-2; isobutane and the product formed by condensation of butene and iso-butene from a C4 cut, and called butene-isobutene polymer; iso-butane and a crude C4 cut, at temperatures ranging from -10 to + 30 DEG C. The yield, bromine numbers, anti-knock ratings, &c. of the products are given. The anti-knock ratings may be increased by the addition of tetra-ethyl lead. According to the first and second Provisional Specifications, the iso-paraffin may be replaced by a naphthene containing a tertiary carbon atom.ALSO:An aviation or motor spirit or constituent thereof is obtained by the alkylation of an iso-paraffin. Iso-butane or iso-pentane is condensed with an olefine, e.g. propylene, iso- or n-butane or the lower polymerides thereof, in the presence of sulphuric acid at low temperatures, e.g. -10 to +30 DEG C., and in substantially equimolecular proportions. Normal paraffins or inert hydrocarbons may be present, but preferably aromatic hydrocarbons are absent. The anti-knock ratings of the products may be increased by the addition of tetra-ethyl lead.
GB2101136A 1936-07-29 1936-07-29 Improvements relating to the production of motor fuel Expired GB479345A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2101136A GB479345A (en) 1936-07-29 1936-07-29 Improvements relating to the production of motor fuel

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2101136A GB479345A (en) 1936-07-29 1936-07-29 Improvements relating to the production of motor fuel

Publications (1)

Publication Number Publication Date
GB479345A true GB479345A (en) 1938-01-31

Family

ID=10155673

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2101136A Expired GB479345A (en) 1936-07-29 1936-07-29 Improvements relating to the production of motor fuel

Country Status (1)

Country Link
GB (1) GB479345A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2420369A (en) * 1938-06-25 1947-05-13 Texas Co Acid alkylation of isoparaffins
US2433944A (en) * 1938-11-05 1948-01-06 Standard Oil Dev Co Method for continuously reacting saturated tertiary hydrocarbons and olefines
US2435029A (en) * 1939-01-03 1948-01-27 Union Oil Co Process for alkylation of isoparaffins with olefins
US2435028A (en) * 1938-07-12 1948-01-27 Union Oil Co Alkylation process
US2435402A (en) * 1938-12-14 1948-02-03 Shell Dev Production of motor fuels
US2567283A (en) * 1938-06-25 1951-09-11 Texas Co Method of manufacturing motor fuels by polymerization and alkylation
EP1340800A1 (en) * 2000-10-11 2003-09-03 Nippon Oil Corporation Dual purpose fuel for gasoline-driven automobile and fuel cell system, and system for storage and/or supply thereof
US7462207B2 (en) 1996-11-18 2008-12-09 Bp Oil International Limited Fuel composition
US8232437B2 (en) 1996-11-18 2012-07-31 Bp Oil International Limited Fuel composition

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2420369A (en) * 1938-06-25 1947-05-13 Texas Co Acid alkylation of isoparaffins
US2567283A (en) * 1938-06-25 1951-09-11 Texas Co Method of manufacturing motor fuels by polymerization and alkylation
US2435028A (en) * 1938-07-12 1948-01-27 Union Oil Co Alkylation process
US2433944A (en) * 1938-11-05 1948-01-06 Standard Oil Dev Co Method for continuously reacting saturated tertiary hydrocarbons and olefines
US2435402A (en) * 1938-12-14 1948-02-03 Shell Dev Production of motor fuels
US2435029A (en) * 1939-01-03 1948-01-27 Union Oil Co Process for alkylation of isoparaffins with olefins
US7553404B2 (en) 1996-11-18 2009-06-30 Bp Oil International Limited Fuel composition
US7462207B2 (en) 1996-11-18 2008-12-09 Bp Oil International Limited Fuel composition
US7833295B2 (en) 1996-11-18 2010-11-16 Bp Oil International Limited Fuel composition
US8232437B2 (en) 1996-11-18 2012-07-31 Bp Oil International Limited Fuel composition
US8536389B2 (en) 1996-11-18 2013-09-17 Bp Oil International Limited Fuel composition
EP1340800A4 (en) * 2000-10-11 2004-10-06 Nippon Oil Corp Dual purpose fuel for gasoline-driven automobile and fuel cell system, and system for storage and/or supply thereof
EP1340800A1 (en) * 2000-10-11 2003-09-03 Nippon Oil Corporation Dual purpose fuel for gasoline-driven automobile and fuel cell system, and system for storage and/or supply thereof

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