GB479345A - Improvements relating to the production of motor fuel - Google Patents
Improvements relating to the production of motor fuelInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/54—Preparation 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
- C07C2/56—Addition to acyclic hydrocarbons
- C07C2/58—Catalytic processes
- C07C2/62—Catalytic processes with acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2527/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- C07C2527/02—Sulfur, selenium or tellurium; Compounds thereof
- C07C2527/053—Sulfates or other compounds comprising the anion (SnO3n+1)2-
- C07C2527/054—Sulfuric 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.
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)
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 |
-
1936
- 1936-07-29 GB GB2101136A patent/GB479345A/en not_active Expired
Cited By (13)
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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