GB606863A - An improved process for the synthesis of hydrocarbons - Google Patents
An improved process for the synthesis of hydrocarbonsInfo
- 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- withdrawn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
Links
- 230000015572 biosynthetic process Effects 0.000 title abstract 5
- 238000003786 synthesis reaction Methods 0.000 title abstract 5
- 229930195733 hydrocarbon Natural products 0.000 title abstract 3
- 150000002430 hydrocarbons Chemical class 0.000 title abstract 3
- 238000000034 method Methods 0.000 title 1
- 239000003054 catalyst Substances 0.000 abstract 24
- 239000007789 gas Substances 0.000 abstract 14
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract 8
- 238000006243 chemical reaction Methods 0.000 abstract 4
- 229910052742 iron Inorganic materials 0.000 abstract 4
- 239000000725 suspension Substances 0.000 abstract 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract 2
- 229910052783 alkali metal Inorganic materials 0.000 abstract 2
- 150000001340 alkali metals Chemical class 0.000 abstract 2
- 239000004411 aluminium Substances 0.000 abstract 2
- 229910052782 aluminium Inorganic materials 0.000 abstract 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract 2
- 239000010941 cobalt Substances 0.000 abstract 2
- 229910017052 cobalt Inorganic materials 0.000 abstract 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 abstract 2
- 239000010949 copper Substances 0.000 abstract 2
- 229910052802 copper Inorganic materials 0.000 abstract 2
- 239000007788 liquid Substances 0.000 abstract 2
- 239000000463 material Substances 0.000 abstract 2
- 239000002245 particle Substances 0.000 abstract 2
- 239000000376 reactant Substances 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C1/00—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
- C07C1/02—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon from oxides of a carbon
- C07C1/04—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon from oxides of a carbon from carbon monoxide with hydrogen
- C07C1/0425—Catalysts; their physical properties
- C07C1/045—Regeneration
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.
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)
| 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 |
-
1946
- 1946-01-21 GB GB203846A patent/GB606863A/en not_active Expired
Cited By (2)
| 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 |
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