GB744687A - Improvements in or relating to fluidized hydroforming process - Google Patents
Improvements in or relating to fluidized hydroforming processInfo
- Publication number
- GB744687A GB744687A GB18094/53A GB1809453A GB744687A GB 744687 A GB744687 A GB 744687A GB 18094/53 A GB18094/53 A GB 18094/53A GB 1809453 A GB1809453 A GB 1809453A GB 744687 A GB744687 A GB 744687A
- Authority
- GB
- United Kingdom
- Prior art keywords
- catalyst
- gas
- regenerator
- regeneration
- plate
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G35/00—Reforming naphtha
- C10G35/04—Catalytic reforming
- C10G35/10—Catalytic reforming with moving catalysts
- C10G35/14—Catalytic reforming with moving catalysts according to the "fluidised-bed" technique
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Catalysts (AREA)
Abstract
<PICT:0744687/III/1> In a hydroforming process wherein hydrocarbon fractions are contacted with a dense fluidized catalyst which is continually withdrawn and regenerated in a fluidized state whereby carbonaceous deposits are burnt therefrom, the spent catalyst particles are maintained under regenerative conditions in the regeneration zone for at least 35 minutes and preferably for 1 to 5 hours. The extended regeneration time can be achieved by enlarging the regenerator to increase holding time or by using a plate column regenerator wherein spent catalyst is supplied to the top of the column and passed via downcomers from plate to plate countercurrent to the regenerating gas which is supplied below the lowest plate at such a velocity as to maintain a dense fluidized bed of catalyst on each plate. Cooling coils may be provided at one or more of the plates to control the temperature. In an alternative regenerator, Fig. 2, spent catalyst suspended in air or other carrier gas is introduced through cone 112 into the upper zone of regenerator vessel 110, the remainder of the regeneration gas being introduced via nozzles in the vicinity of 112 and through distribution cone 115 at a velocity, e.g. 0.6-1.0 ft. per second, sufficient to form a dense fluidized bed of catalyst 116 in said upper zone. The average time of residence in this upper zone is less than 15 minutes and may be as little as 3-5 minutes. The portion of the regenerator below 112 is a low velocity zone, provided with baffles 123 and 124, through which the velocity of regeneration gas is sufficient only to maintain fluidity so as to ensure countercurrent contact between gas and catalyst, and wherein the catalyst is maintained in contact with the said gas for at least 35 minutes. The regeneration temperature in the upper zone may be controlled by passing water or other heat-exchange fluid through cooling jacket 130. Alternatively an arrangement of cooling coils with a primary coil entirely below the dense bed level and a secondary coil partly above and partly below, may be used, permitting adjustment of heat-exchange by variation of bed level. The regenerator is operated at 50-500 lbs. per sq. inch pressure and at temperatures of 1050-1200 DEG F. preferably 1075-1125 DEG F. The regeneration gas may be air but air diluted with flue gas to 1 to 5 per cent O2 concentration is preferred. Suitable catalysts include Group VI metal oxides such as molybdenum, chromium or tungsten oxide, or mixtures thereof, preferably supported on activated alumina or zinc spinel. Minor amounts of promoters such as silica, calcium oxide, ceria or potassium oxide may be included in the catalyst.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US744687XA | 1952-08-29 | 1952-08-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB744687A true GB744687A (en) | 1956-02-15 |
Family
ID=22119724
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB18094/53A Expired GB744687A (en) | 1952-08-29 | 1953-06-30 | Improvements in or relating to fluidized hydroforming process |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB744687A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2233663A (en) * | 1989-07-12 | 1991-01-16 | Exxon Research Engineering Co | Catalyst stripper unit and process in catalytic cracking operations |
CN110639435A (en) * | 2019-11-11 | 2020-01-03 | 清华大学 | Inner member and multistage fluidized bed reactor |
-
1953
- 1953-06-30 GB GB18094/53A patent/GB744687A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2233663A (en) * | 1989-07-12 | 1991-01-16 | Exxon Research Engineering Co | Catalyst stripper unit and process in catalytic cracking operations |
WO1991000899A1 (en) * | 1989-07-12 | 1991-01-24 | Exxon Research And Engineering Company | Catalyst stripper unit and process in catalytic cracking operations |
AU639472B2 (en) * | 1989-07-12 | 1993-07-29 | Exxon Research And Engineering Company | Catalyst stripper unit and process in catalytic cracking operations |
CN110639435A (en) * | 2019-11-11 | 2020-01-03 | 清华大学 | Inner member and multistage fluidized bed reactor |
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