[go: up one dir, main page]

GB606863A - An improved process for the synthesis of hydrocarbons - Google Patents

An improved process for the synthesis of hydrocarbons

Info

Publication number
GB606863A
GB606863A GB203846A GB203846A GB606863A GB 606863 A GB606863 A GB 606863A GB 203846 A GB203846 A GB 203846A GB 203846 A GB203846 A GB 203846A GB 606863 A GB606863 A GB 606863A
Authority
GB
United Kingdom
Prior art keywords
reactor
catalyst
line
withdrawn
gases
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
GB203846A
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.)
Standard Oil Development Co
Original Assignee
Standard Oil Development Co
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 Standard Oil Development Co filed Critical Standard Oil Development Co
Priority to GB203846A priority Critical patent/GB606863A/en
Publication of GB606863A publication Critical patent/GB606863A/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
    • C07C1/0425Catalysts; their physical properties
    • C07C1/045Regeneration

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)
  • Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

<PICT:0606863/III/1> In the synthesis of liquid hydrocarbons from CO+H2 using a fluidized catalyst, contaminated catalyst is withdrawn from the reaction zone, either continuously or intermittently, heated to volatilize oily or waxy material, and returned. A stripping gas may be used to assist the volatilization which is effected in a second reaction zone. The reactors 1, 1a are of the usual type wherein the catalyst is kept in a fluidized state by controlling the net upward velocity of the reacting gases at 1/2 -5 ft./sec. for a particle size of 100-400 mesh. Catalyst is withdrawn through lines 3, 3a and cooled in coolers 4, 4a, while reactants are withdrawn through lines 6, 6a, treated to remove residues of catalyst, condensed in coolers 7, 7a and collected in drums 10, 10a. Synthesis gas enters by line 2 and heater 5. Catalyst withdrawn from reactor 1 is in part returned via lines 12 and 2, and in part passed by line 14, after suspension in uncondensed gases from drum 10 supplied by line 15, through heater 20 to reactor 1a. The said gases may first be freed from CO2 in scrubber S, and act to strip oil and wax from the catalyst in reactor 1a which is operated at a lower pressure and higher temperature. Stripping is assisted by gases from drum 10a which are fed via line 22, and heater 24 to reactor 1a, and carry in suspension catalyst recovered from cooler 4a via line 26. Other catalyst from 4a is fed by line 30 to feed line 2 of reactor 1. Gases from 10a may pass by pipe 40 and cooler 41 to a drum 10b. Product and water are separately withdrawn from drums 10, 10a, 10b. Reactor 1a is preferably of about one-third the volume of reactor 1. Suitable catalysts contain cobalt-magnesia-kieselguhr, e.g. 32, 5, 63 per cent by weight, or over 45 per cent iron with, say, 5 per cent oxide of alkali metal, copper or aluminium. With the former, operating conditions in reactor 1 are 375-450 DEG F., 10-150 p.s.i.g., and 500-500 vols./vol./hr.; with the latter, 450-700 DEG F., 50-500 p.s.i.g., and 50-100 vols./vol./hr. In reactor 1a, temperature is 5-100 DEG F. higher, and pressure 10-150 p.s.i.g. lower than in reactor 1, for cobalt catalysts. For iron catalysts, the figures are 5-250 and 50-500. Specification 600,580 is referred to.ALSO:<PICT:0606863/IV(b)/1> In the synthesis of liquid hydrocarbons from CO+H2 using a fluidized catalyst, contaminated catalyst is withdrawn from the reaction zone, either continuously or intermittently, heated to volatilize oily or waxy material and returned. A stripping gas may be used to assist the volatilization which is effected in a second reaction zone. The reactors 1, 1a are of the usual type, wherein the catalyst is kept in a fluidized state by controlling the net upward velocity of the reacting gases at 1/2 -5 p ft./sec. for a particle size of 100-400 mesh. Catalyst is withdrawn through lines 3, 3a, and cooled in coolers 4, 4a, while reactants are withdrawn through lines 6, 6a, treated to remove residues of catalyst, condensed in coolers 7, 7a, and collected in drums 10, 10a. Synthesis gas enters by line 2 and heater 5. Catalyst withdrawn from reactor 1 is in part returned via lines 12 and 2, and in part passed by line 14, after suspension in uncondensed gases from drum 10 supplied by line 15, through heater 20 to reactor 1a. The said gases may first be freed from CO2 in scrubber S, and act to strip oil and wax from the catalyst in reactor 1a which is operated at a lower pressure and higher temperature. Stripping is assisted by gases from drum 10a which are fed via line 22, and heater 24 to reactor 1a, and carry in suspension catalyst recovered from cooler 4a via line 26. Other catalyst from 4a is fed by line 30 to feed line 2 of reactor 1. Gases from 10a may also pass by pipe 40 and cooler 41 to a drum 10b. Product and water are separately withdrawn from drums 10, 10a, 10b. Reactor 1a is preferably of about one-third the volume of reactor 1. Suitable catalysts contain cobalt-magnesia-kieselguhr, e.g. 32, 5, 63 per cent by weight, or over 45 per cent iron with say 5 per cent oxide of alkali metal, copper or aluminium. With the former, operating conditions in reactor 1 are 375-450 DEG F., 10-150 p.s.i.g., and 50-500 vols./vol./hr.; with the latter, 450-700 DEG F., 50-500 p.s.i.g., and 50-1000 vols./vol./hr. In reactor 1a, temperature is 5-100 DEG F. higher, and pressure 10-150 p.s.i.g. lower than in reactor 1, for cobalt catalysts. For iron catalysts, the figures are 5-250 and 50-500. Specification 600,580 is referred to.
GB203846A 1946-01-21 1946-01-21 An improved process for the synthesis of hydrocarbons Expired GB606863A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB203846A GB606863A (en) 1946-01-21 1946-01-21 An improved process for the synthesis of hydrocarbons

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB203846A GB606863A (en) 1946-01-21 1946-01-21 An improved process for the synthesis of hydrocarbons

Publications (1)

Publication Number Publication Date
GB606863A true GB606863A (en) 1948-08-20

Family

ID=9732510

Family Applications (1)

Application Number Title Priority Date Filing Date
GB203846A Expired GB606863A (en) 1946-01-21 1946-01-21 An improved process for the synthesis of hydrocarbons

Country Status (1)

Country Link
GB (1) GB606863A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0015715A1 (en) * 1979-03-01 1980-09-17 Mobil Oil Corporation Conversion of lower alcohols and ether derivatives thereof into hydrocarbons in a baffled reactor system
WO2001028962A1 (en) * 1999-10-15 2001-04-26 Exxon Research And Engineering Company Process for the preparation of high activity carbon monoxide hydrogenation catalyst and the catalyst composition obtained

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0015715A1 (en) * 1979-03-01 1980-09-17 Mobil Oil Corporation Conversion of lower alcohols and ether derivatives thereof into hydrocarbons in a baffled reactor system
WO2001028962A1 (en) * 1999-10-15 2001-04-26 Exxon Research And Engineering Company Process for the preparation of high activity carbon monoxide hydrogenation catalyst and the catalyst composition obtained

Similar Documents

Publication Publication Date Title
US2309034A (en) Method for cooling fluid catalysts
US2451879A (en) Hydrocarbon synthesis
US2472219A (en) Synthesis of hydrocarbons
US2482284A (en) Production of oxygenated compounds and liquid hydrocarbons from hydrocarbon gases
US4263141A (en) Process of producing gasoline from synthesis gas
US5004862A (en) Process for recycling and purifying condensate from a hydrocarbon or alcohol synthesis process
US2527846A (en) Hydrogen-carbon monoxide synthesis
US4256654A (en) Conversion of hydrogen and carbon monoxide into C1 -C4 range hydrocarbons
US2486693A (en) Method for the synthesis of carbinols
GB606863A (en) An improved process for the synthesis of hydrocarbons
US2529630A (en) Process for the manufacture of synthesis gases
US1858822A (en) Process for the treating of hydrocarbon materials
US2465462A (en) Catalytic synthesis of hydrocarbons
US2885267A (en) Method of producing hydrogen and carbon black
US2640843A (en) Synthesis of organic compounds
GB1457065A (en) Photochemical method of preparing hydrocarbon derivarives
US2662912A (en) Hydrocarbon synthesis reaction
US2631094A (en) Natural gas conversion to hydrogen and carbon monoxide
US4242234A (en) Catalyst for conversion of hydrogen and carbon monoxide into C1 -C.sub.
US2728638A (en) Process for the manufacture of carbonyl sulfide
US2558760A (en) Hydrocarbon synthesis
US2560171A (en) Synthesis of organic compounds
GB647363A (en) Improvements in or relating to production of oxygenated organic compounds from olefins
US4252685A (en) Catalysts comprising halogenated, reduced iron oxide-potassium carbonate for conversion of hydrogen and carbon monoxide into C1 -C4 range hydrocarbons
GB655827A (en) Improved hydrocarbon synthesis