GB540824A - A process for the production of hydrocarbons - Google Patents

A process for the production of hydrocarbons

Info

Publication number
GB540824A
GB540824A GB31807/39A GB3180739A GB540824A GB 540824 A GB540824 A GB 540824A GB 31807/39 A GB31807/39 A GB 31807/39A GB 3180739 A GB3180739 A GB 3180739A GB 540824 A GB540824 A GB 540824A
Authority
GB
United Kingdom
Prior art keywords
pipe
olefines
dispersion
isoparaffins
hydrocarbons
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
GB31807/39A
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.)
Bataafsche Petroleum Maatschappij NV
Original Assignee
Bataafsche Petroleum Maatschappij NV
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 Bataafsche Petroleum Maatschappij NV filed Critical Bataafsche Petroleum Maatschappij NV
Publication of GB540824A publication Critical patent/GB540824A/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

540,824. Aliphatic hydrocarbons. NAAMLOOZE VENNOOTSCHAP DE BATAAFSCHE PETROLEUM MAATSCHAPPIJ. Dec. 8, 1939, Nos. 31807 and 31808. Convention dates, Dec. 14, 1938, and May 27, 1939. [Class 2 (iii)] Olefines having at least six carbon atoms in the molecule are continuously fed into a circulating dispersion of isoparaffin and 85 to 110 per cent sulphuric acid at such a rate that the molar ratio of isoparaffins to olefines in the dispersion at the point of introduction of the olefines is at least 2:1, a portion of the dispersion is continuously withdrawn at a point where substantially no olefines remain unreacted, the desired hydrocarbon products are removed from the dispersion thus withdrawn and the unreacted isoparaffins are returned to the circulating dispersion. The reaction is conducted at 50-20 to 50‹C. and the olefines are advantageously diluted with isoparaffins before their introduction. In Fig. 1, the isoparaffins and olefines are fed into the system by pipes 1, 2 respectively and they pass by line 3 and valve 4 into a re-cycled dispersion of sulphuric acid and hydrocarbons in line 5. Isoparaffins may be fed into line 3 by means of pipe 25 or pipe 32. The dispersion is pumped into a reaction chamber 10 by pump 6 and is returned to line 5 by pipe 15. Before entering the reaction tank 10 a part of the circulating mixture passes to a cooler 12. Part of the circulating dispersion is led to a separator 17, the acid portion passing to the pump 6 and the hydrocarbons to a still 27. Some of the hydrocarbons may be used to dilute the olefine feed by returning them through pipe 25. From still 27, unreacted isoparaffins pass by pipe 30 to the olefinic feed. When it is desired to remove normal butane and other inert constituents, the vapour from still 27 is passed to a still 31, the inert constituent leaving by pipe 33. In a modified process employing cracked gasoline as the olefine, a mixing tank 2, Fig. 2, is supplied with cracked gasoline through pipe 1 and isopentane and/or isobutane through pipe 3, and the resulting hydrocarbon mixture containing large excess of isoparaffin is introduced through pipe 6 into a circulating stream of sulphuric acid and hydrocarbons substantially free of olefines flowing in pipe 7 to a pump 8 which forces the mixture through a mixing device 10 to a tank 12. The dispersion, after cooling, then passes to a settling tank 15 or is returned to pipe 7. From the settling tank the acid is returned to pipe 7 and the hydrocarbon product passes either to the mixer 2 through pipe 4 or to a scrubber 21 in which it is treated with caustic alkali. The scrubbed products enter a fractionating column 24, the low boiling constituents being returned directly to pipe 4 through pipe 26 if they are free from inert constituents, and, when they contain the latter, first to fractionating column 28 and then to pipe 4. Debutanized gasoline withdrawn from column 24 is finally freed from heavy products in a column 32. In a further example, a re-formed aviation gasoline containing 28 per cent of olefines which has been treated with phosphoric acid is subjected to the above process. The olefines may be natural in origin or be obtained by catalytic dehydrogenation, cracking or other pyrogenic treatment. Benzene sulphonic acid and heavy metal sulphates are stated to assist the reaction. Specifications 515,367, 526,149 and 531,383 are referred to.
GB31807/39A 1938-12-14 1939-12-08 A process for the production of hydrocarbons Expired GB540824A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US540824XA 1938-12-14 1938-12-14

Publications (1)

Publication Number Publication Date
GB540824A true GB540824A (en) 1941-10-31

Family

ID=21988685

Family Applications (1)

Application Number Title Priority Date Filing Date
GB31807/39A Expired GB540824A (en) 1938-12-14 1939-12-08 A process for the production of hydrocarbons

Country Status (1)

Country Link
GB (1) GB540824A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2423401A (en) * 1943-03-16 1947-07-01 Socony Vacuum Oil Co Inc Alkylation of isoparaffins
US2465049A (en) * 1945-01-08 1949-03-22 Phillips Petroleum Co Alkylation of hydrocarbons
EP0584006A1 (en) * 1992-08-20 1994-02-23 Institut Francais Du Petrole Process for the alkylation of paraffins
FR2705665A1 (en) * 1993-05-26 1994-12-02 Inst Francais Du Petrole Process for the alkylation of paraffins

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2423401A (en) * 1943-03-16 1947-07-01 Socony Vacuum Oil Co Inc Alkylation of isoparaffins
US2465049A (en) * 1945-01-08 1949-03-22 Phillips Petroleum Co Alkylation of hydrocarbons
EP0584006A1 (en) * 1992-08-20 1994-02-23 Institut Francais Du Petrole Process for the alkylation of paraffins
US5444175A (en) * 1992-08-20 1995-08-22 Institut Francais Du Petrole Process for the alkylation of paraffins
FR2705665A1 (en) * 1993-05-26 1994-12-02 Inst Francais Du Petrole Process for the alkylation of paraffins

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