GB647155A - Improvements in or relating to a process of synthesizing hydrocarbons - Google Patents

Improvements in or relating to a process of synthesizing hydrocarbons

Info

Publication number
GB647155A
GB647155A GB21865/47A GB2186547A GB647155A GB 647155 A GB647155 A GB 647155A GB 21865/47 A GB21865/47 A GB 21865/47A GB 2186547 A GB2186547 A GB 2186547A GB 647155 A GB647155 A GB 647155A
Authority
GB
United Kingdom
Prior art keywords
catalyst
gas
gases
products
returned
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
GB21865/47A
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 Co
Original Assignee
Standard Oil 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 Co filed Critical Standard Oil Co
Publication of GB647155A publication Critical patent/GB647155A/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
    • C07C1/0465Reaction conditions concerning fluidisation

Abstract

<PICT:0647155/IV (b)/1> <PICT:0647155/IV (b)/2> <PICT:0647155/IV (b)/3> Hydrocarbons and oxygenated compounds are synthesized by introducing a gas mixture comprising carbon monoxide and hydrogen into the base of a reaction zone containing finely-divided synthesis catalyst and passing the gas upwardly at a low velocity to maintain the catalyst in suspended dense phase liquid-like condition, unreacted gases and reaction products being separated from catalyst, and unreacted gases and normally gaseous products removed from heavier products. With a catalyst bulk density of 10-40 lbs./c.ft., a gas velocity of about 0.1-10 generally 0.5-1.5 ft./sec. is used. A catalyst particle size of about 100-400 mesh or smaller is suitable. Gaseous hydrocarbons, e.g. natural gas, may be desulphurized and passed with carbon dioxide and steam over a Group 8 metal oxide, especially oxides of Ni, Fe, and Mn in proportions by weight of 1 : 1 : 0.5, to give a 2 : 1 hydrogen to carbon monoxide mixture. The heat necessary may be obtained by burning part of the initial hydrocarbon gas mixed with part of the recycled gases. The synthesis temperature is controlled by cooling catalyst or synthesis gas outside the reaction zone. The reactor 45, Fig. 1, may be funnel-shaped at top and bottom, a pipe 49 extending into an enlarged settling chamber 50. Primary cyclone separators 52 pick up through inlets 53, gases from which the bulk of the catalyst has settled, the removed catalyst being returned through dip legs 54, and the gases passing to secondary separators 56. The settled catalyst is maintained fluent and freed from deposited hydrocarbons by injecting hot stripping gas through lines 58 or a perforated annular pipe 59, and is fed to the lower part of the reactor through cooling tubes 60 having cooling jackets 68. To disperse the returned catalyst in the up-flowing gas and aerate that in the cooling tubes, conical-shaped ported members 61 are fed with inert gas through lines 64. In a modification, Fig. 3, the reactor is surrounded by an annular chamber containing tubes 60 and extended to surround the base, the catalyst being suspended by gas introduced by line 44 and its rate of flow controlled by a valve 61a. In a further modification, Fig. 4, the catalyst from settling zone 50 may be discharged through standpipe 67 surrounded by cooling jacket 68 and returned through valve 69 to the inlet gas stream from pipe 44 or may be recycled through pipe 71 to heat exchanger 72 and returned by any of lines 77 in an inert gas from line 75. Gases separated from the products may be fed to a second synthesis stage. Gasoline or naphtha products may be reformed and heavy products cracked. Gases may be polymerized or alkylated. Specification 558,879 is referred to.ALSO:<PICT:0647155/III/1> <PICT:0647155/III/2> <PICT:0647155/III/3> Hydrocarbons and oxygenated compounds are synthesized by introducing a gas mixture comprising carbon monoxide and hydrogen into the base of a reaction zone containing finely-divided synthesis catalyst and passing the gas upwardly at a low velocity to maintain the catalyst in suspended dense phase liquid-like condition, unreacted gases and reaction products being separated from catalyst, and unreacted gases and normally gaseous products removed from heavier products. With a catalyst bulk density of 10-40 lbs./c. ft., a gas velocity of about .1-10, generally .5-1.5 ft./sec. is used. A catalyst particle size of about 100-400 mesh or smaller is suitable. Gaseous hydrocarbons, e.g. natural gas, may be desulphurized and passed with carbon dioxide and steam over a Group 8 metal oxide, especially oxides of Ni, Fe, and Mn in proportions by weight of 1 : 1; 0.5, to give a 2 : 1 hydrogen to carbon monoxide mixture. The heat necessary may be obtained by burning part of the initial hydrocarbon gas mixed with part of the recycled gases. The synthesis temperature is controlled by cooling catalyst or synthesis gas outside the reaction zone. The reactor 45, Fig. 1, may be funnel-shaped at top and bottom, a pipe 49 extending into an enlarged settling chamber 50. Primary cyclone separators 52 pick up through inlets 53, gases from which the bulk of the catalyst has settled, the removed catalyst being returned through dip legs 54, and the gases passing to secondary separators 56. The settled catalyst is maintained fluent and freed from deposited hydrocarbons by injecting hot stripping gas through lines 58 or a perforated annular pipe 59, and is fed to the lower part of the reactor through cooling tubes 60 having cooling jackets 68. To disperse the returned catalyst in the upflowing gas and aerate that in the cooling tubes, conical-shaped ported members 61 are fed with inert gas through lines 64. In a modification, Fig. 3, the reactor is surrounded by an annular chamber containing tubes 60 and extended to surround the base, the catalyst being suspended by gas introduced by line 44 and its rate of flow controlled by a valve 61a. In a further modification, Fig. 4, the catalyst from settling zone 50 may be discharged through standpipe 67 surrounded by cooling jacket 68 and returned through valve 69 to the inlet gas stream from pipe 44 or may be recycled through pipe 71 to heat exchanger 72 and returned by any of lines 77 in an inert gas from line 75. Gases separated from the products may be fed to a second synthesis stage. Gasoline or naphtha products may be reformed and heavy products cracked. Gases may be polymerized or alkylated. Specification 558,879 is referred to.
GB21865/47A 1941-04-24 1947-08-08 Improvements in or relating to a process of synthesizing hydrocarbons Expired GB647155A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US647155XA 1941-04-24 1941-04-24

Publications (1)

Publication Number Publication Date
GB647155A true GB647155A (en) 1950-12-06

Family

ID=22057811

Family Applications (1)

Application Number Title Priority Date Filing Date
GB21865/47A Expired GB647155A (en) 1941-04-24 1947-08-08 Improvements in or relating to a process of synthesizing hydrocarbons

Country Status (1)

Country Link
GB (1) GB647155A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011015664A3 (en) * 2009-08-06 2011-03-31 Shell Internationale Research Maatschappij B.V. Method for revamping an hf or sulphuric acid alkylation unit
WO2011015662A3 (en) * 2009-08-06 2011-03-31 Shell Internationale Research Maatschappij B.V. Method for revamping an hf or sulphuric acid alkylation unit
CN102510849A (en) * 2009-08-06 2012-06-20 中国石油大学(北京) Method for revamping an HF or sulphuric acid alkylation unit
CN102510850A (en) * 2009-08-06 2012-06-20 中国石油大学(北京) Method for revamping an HF or sulphuric acid alkylation unit
US9260668B2 (en) 2009-07-17 2016-02-16 Shell Oil Company Method for revamping an HF or sulphuric acid alkylation unit and method for the production of alkylate

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9260668B2 (en) 2009-07-17 2016-02-16 Shell Oil Company Method for revamping an HF or sulphuric acid alkylation unit and method for the production of alkylate
WO2011015664A3 (en) * 2009-08-06 2011-03-31 Shell Internationale Research Maatschappij B.V. Method for revamping an hf or sulphuric acid alkylation unit
WO2011015662A3 (en) * 2009-08-06 2011-03-31 Shell Internationale Research Maatschappij B.V. Method for revamping an hf or sulphuric acid alkylation unit
CN102510849A (en) * 2009-08-06 2012-06-20 中国石油大学(北京) Method for revamping an HF or sulphuric acid alkylation unit
CN102510850A (en) * 2009-08-06 2012-06-20 中国石油大学(北京) Method for revamping an HF or sulphuric acid alkylation unit
US8569561B2 (en) 2009-08-06 2013-10-29 Shell Oil Company Method for revamping an HF or sulphuric acid alkylation unit
AU2010280718B2 (en) * 2009-08-06 2013-11-14 Shell Internationale Research Maatschappij B.V. Method for revamping an HF or sulphuric acid alkylation unit
CN102510849B (en) * 2009-08-06 2013-12-18 中国石油大学(北京) Method for revamping HF or sulphuric acid alkylation unit
AU2010280718B8 (en) * 2009-08-06 2014-03-13 Shell Internationale Research Maatschappij B.V. Method for revamping an HF or sulphuric acid alkylation unit
AU2010280718A8 (en) * 2009-08-06 2014-03-13 Shell Internationale Research Maatschappij B.V. Method for revamping an HF or sulphuric acid alkylation unit
CN102510850B (en) * 2009-08-06 2014-04-23 中国石油大学(北京) Method for revamping an HF or sulphuric acid alkylation unit

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