GB547214A - Improvements in or relating to the alkylation of hydrocarbons - Google Patents

Improvements in or relating to the alkylation of hydrocarbons

Info

Publication number
GB547214A
GB547214A GB823140A GB823140A GB547214A GB 547214 A GB547214 A GB 547214A GB 823140 A GB823140 A GB 823140A GB 823140 A GB823140 A GB 823140A GB 547214 A GB547214 A GB 547214A
Authority
GB
United Kingdom
Prior art keywords
hydrocarbons
passed
alkylation
fraction
pipe
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
GB823140A
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.)
Texaco Development Corp
Original Assignee
Texaco Development Corp
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 Texaco Development Corp filed Critical Texaco Development Corp
Priority to GB823140A priority Critical patent/GB547214A/en
Publication of GB547214A publication Critical patent/GB547214A/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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Abstract

547,214. Alkylation of hydrocarbons. STEVENS, A. H. (Texaco Development Corporation). May 7, 1940, No. 8231. [A Specification was laid open to inspection under Sect. 91 of the Acts, Nov. 12, 1940]. [Class 2 (iii)] Isoparaffin hydrocarbons are alkylated with C 3 and C 4 olefins by subjecting a C 4 olefin containing fraction and a low boiling isoparaffin to contact with a liquid alkylation catalyst in a reaction zone under a pressure just sufficient to maintain the C 4 hydrocarbons in the liquid state but insufficient to liquefy the C 3 hydrocarbons. At the same time C 3 hydrocarbons which have been either separated off from the above C 4 fraction, or supplied from a separate source are contacted with a liquid alkylation catalyst in a separate absorption zone, and the liquid product supplied to the above alkylation reaction zone. The isoparaffin is thus alkylated with C 3 and C 4 hydrocarbons using a pressure not greater than that necessary to maintain C 4 hydrocarbons in the liquid state. Saturated C 3 hydrocarbons which are not absorbed in the C 3 absorption zone are rejected. In a preferred form of the invention the process is operated as a continuous multistage process, and catalyst discharged from the reaction zone is passed to the separate C 3 absorption zone, each alkylation stage having its own individual absorption stage. In an example an unstabilized cracked naphtha is passed from pipe 1 to stabilizer 2, and a distillate comprising C 4 , C 3 and lighter hydrocarbons is passed to a fractionator 4 when the C 3 fraction is separated from the C 4 . The C 4 fraction is passed to reactor 6 where it is contacted with isobutane in the presence of concentrated sulphuric acid. The reaction mixture from 6 passes to settler 8 where the used acid separates. At least a substantial portion thereof is mixed in a mixing coil 10 with C 3 and lighter hydrocarbons from pipe 11. The product from mixing coil 10 passes upwards through absorber 14. Fresh sulphuric acid is added to the absorber through pipe 15. Unabsorbed C 3 and lighter hydrocarbons such as propane are discharged through pipe 16. The acid containing the absorbed olefins is passed direct to the reaction vessel 6. The apparatus described has three succeeding stages which function in the same way as the stage just described.
GB823140A 1940-05-07 1940-05-07 Improvements in or relating to the alkylation of hydrocarbons Expired GB547214A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB823140A GB547214A (en) 1940-05-07 1940-05-07 Improvements in or relating to the alkylation of hydrocarbons

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB823140A GB547214A (en) 1940-05-07 1940-05-07 Improvements in or relating to the alkylation of hydrocarbons

Publications (1)

Publication Number Publication Date
GB547214A true GB547214A (en) 1942-08-19

Family

ID=9848477

Family Applications (1)

Application Number Title Priority Date Filing Date
GB823140A Expired GB547214A (en) 1940-05-07 1940-05-07 Improvements in or relating to the alkylation of hydrocarbons

Country Status (1)

Country Link
GB (1) GB547214A (en)

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