GB676635A - Improvements in or relating to hydrocarbon synthesis - Google Patents

Improvements in or relating to hydrocarbon synthesis

Info

Publication number
GB676635A
GB676635A GB1539449A GB1539449A GB676635A GB 676635 A GB676635 A GB 676635A GB 1539449 A GB1539449 A GB 1539449A GB 1539449 A GB1539449 A GB 1539449A GB 676635 A GB676635 A GB 676635A
Authority
GB
United Kingdom
Prior art keywords
per cent
products
catalyst
reaction
feed
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
GB1539449A
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.)
Hydrocarbon Research Inc
Original Assignee
Hydrocarbon Research Inc
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 Hydrocarbon Research Inc filed Critical Hydrocarbon Research Inc
Priority to GB1539449A priority Critical patent/GB676635A/en
Publication of GB676635A publication Critical patent/GB676635A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C1/00Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
    • C07C1/02Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon from oxides of a carbon
    • C07C1/04Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon from oxides of a carbon from carbon monoxide with hydrogen
    • C07C1/0455Reaction conditions
    • C07C1/046Numerical values of parameters
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/70Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the iron group metals or copper
    • C07C2523/74Iron group metals
    • C07C2523/745Iron

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

A process of synthesizing hydrocarbons, oxygenated hydrocarbons and mixtures thereof from CO and H2 in the presence of a fluidized iron catalyst, wherein a stream of reactant gas containing a substantial proportion of H2 and CO is passed in contact with said catalyst under predetermined conditions of reaction, including an elevated temperature effective to form such products, a substantial portion of the CO is converted, and the products are withdrawn from contact with the catalyst, is characterized by regulating the time of contact between the reactant gas and the catalyst so that the withdrawn stream of products contains between about 1 and 3 per cent by volume of CO, and recovering the products from the withdrawn stream. Within the stated range it is preferred that the product stream contains not less than about 2 mol. per cent of CO. Advantageously the total mol. per cent of CO in the feed is not substantially greater than about 15 per cent of the total gas feed and is preferably not less than about 5 mol. per cent greater than that in the effiuent. The water content should be as low as possible and not greater than 3 mol. per cent. Preferably the feed contains an H2 : CO ratio of substantially above 2.5 : 1, preferably above 3 : 1, e.g. 4 or 5 : 1. Preferably upwards of about 15 per cent of CO2 should be present. Inert gas diluents may be used and gaseous reaction products recycled. Temperatures, pressures and catalysts usual in the art are employed. Aliphatic alcohols, organic acids, ketones and aldehydes are mentioned as oxygen-containing compounds produced. In an example the catalyst is iron powder with K2O and Al2O3 promoters and is conditioned prior to reaction, the feed is about 30.6 per cent CO, about 64.3 per cent H2, the remainder being CO2, CH4 and N2, reaction is at 650 DEG F. and 250 p.s.i. with a linear gas velocity of 1.2 feet per second, and the effluent gases contain about 2.3 per cent of CO, the contact time being approximately 25 seconds and the products liquid hydrocarbons. In a comparative illustration reaction is effected to give effluent gases containing about 0.7 per cent CO and in a further example, a portion of the effluent, after product separation, is recycled to the fresh feed in a ratio of 1 : 1 and the combined feeds treated as in the first example.
GB1539449A 1949-06-09 1949-06-09 Improvements in or relating to hydrocarbon synthesis Expired GB676635A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1539449A GB676635A (en) 1949-06-09 1949-06-09 Improvements in or relating to hydrocarbon synthesis

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1539449A GB676635A (en) 1949-06-09 1949-06-09 Improvements in or relating to hydrocarbon synthesis

Publications (1)

Publication Number Publication Date
GB676635A true GB676635A (en) 1952-07-30

Family

ID=10058377

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1539449A Expired GB676635A (en) 1949-06-09 1949-06-09 Improvements in or relating to hydrocarbon synthesis

Country Status (1)

Country Link
GB (1) GB676635A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003044128A2 (en) * 2001-11-20 2003-05-30 Exxonmobil Research And Engineering Company Process for maximizing 371°+ production in a fischer-tropsch process

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003044128A2 (en) * 2001-11-20 2003-05-30 Exxonmobil Research And Engineering Company Process for maximizing 371°+ production in a fischer-tropsch process
WO2003044128A3 (en) * 2001-11-20 2004-02-12 Exxonmobil Res & Eng Co Process for maximizing 371°+ production in a fischer-tropsch process
AU2002340136B2 (en) * 2001-11-20 2007-09-06 Exxonmobil Research And Engineering Company Process for maximizing 371degree+ production in a Fischer-Tropsch process

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