GB788000A - Improved method and apparatus for reacting carbon-containing gaseous compounds in the presence of a catalyst - Google Patents

Improved method and apparatus for reacting carbon-containing gaseous compounds in the presence of a catalyst

Info

Publication number
GB788000A
GB788000A GB34928/54A GB3492854A GB788000A GB 788000 A GB788000 A GB 788000A GB 34928/54 A GB34928/54 A GB 34928/54A GB 3492854 A GB3492854 A GB 3492854A GB 788000 A GB788000 A GB 788000A
Authority
GB
United Kingdom
Prior art keywords
catalyst
riser
gas
reactor
per
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
GB34928/54A
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.)
MW Kellogg Co
Original Assignee
MW Kellogg 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 MW Kellogg Co filed Critical MW Kellogg Co
Publication of GB788000A publication Critical patent/GB788000A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING 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
    • C10G11/00Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
    • C10G11/14Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils with preheated moving solid catalysts
    • C10G11/18Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils with preheated moving solid catalysts according to the "fluidised-bed" technique
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J38/00Regeneration or reactivation of catalysts, in general
    • B01J38/04Gas or vapour treating; Treating by using liquids vaporisable upon contacting spent catalyst
    • B01J38/12Treating with free oxygen-containing gas
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/0015Feeding of the particles in the reactor; Evacuation of the particles out of the reactor
    • B01J8/0025Feeding of the particles in the reactor; Evacuation of the particles out of the reactor by an ascending fluid
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/18Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles
    • B01J8/24Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles according to "fluidised-bed" technique
    • B01J8/26Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles according to "fluidised-bed" technique with two or more fluidised beds, e.g. reactor and regeneration installations
    • B01J8/28Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles according to "fluidised-bed" technique with two or more fluidised beds, e.g. reactor and regeneration installations the one above the other
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P30/00Technologies relating to oil refining and petrochemical industry
    • Y02P30/40Ethylene production

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • General Chemical & Material Sciences (AREA)
  • Materials Engineering (AREA)
  • Combustion & Propulsion (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)
  • Devices And Processes Conducted In The Presence Of Fluids And Solid Particles (AREA)

Abstract

<PICT:0788000/III/1> Reactions, e.g. cracking of hydrocarbon oils, are effected by contacting a carbon-containing reactant vaporous at a reaction temperature with a fluidized catalyst (e.g. containing silica and alumina, zirconia, boria or magnesia) in a reaction zone (10), withdrawing contaminated catalyst through a vertical riser (20) in suspension in an oxygen-containing gas to a regeneration zone (11) vertically above the reaction zone, in which it is maintained in fluidized condition by means of an oxygen-containing gas, and returning the regenerated catalyst to the reaction zone by means of a plurality of vertical stand pipes (21, 22) symmetrically arranged round the riser (20). The numerals refer to the apparatus illustrated in Fig. 1 in which the regenerator is supported upon the reactor by means of an intermediate vessel 12 through which air can circulate freely. The regenerator may, however, rest directly on the reactor if it has a diameter less than about 25 feet. The vaporous portion of a hydrocarbon oil such as gas oil, reduced crude, vacuum distillate or solvent decarbonized residual oil having an initial boiling point of 400-600 DEG F., and an end point of 700-1300 DEG F. and an A.P.I. gravity of 10 DEG to 40 DEG , e.g. 25 DEG , may be cracked at 850 DEG to 950 DEG F., e.g. 900 DEG F., by introduction into reactor 10 through nozzles 44, at a pressure of 1 atmosphere to 50 p.s.i.g., preferably 5 to 25 p.s.i.g., a weight space velocity of 0.25 to 15, e.g. 0.5 to 5, and a catalyst to oil ratio of 2 to 25, e.g. 5 to 10 by weight. Thereafter the catalyst may pass via louvres 18 shielded by baffles 19 into a striping zone concentric with the riser and supplied with a stripping gas such as steam, hydrogen, flue gas, carbon dioxide or a normally gaseous hydrocarbon (methane, ethane or propane) maintained at e.g. 5 DEG to 20 DEG F. higher than the reaction zone, e.g. at 800 DEG to 1000 DEG F., usually 875 DEG to 950 DEG F., or in a specific example at 1080 DEG F. The catalyst is then withdrawn by means of the riser 20 and reciprocable valve 27. The riser is sealed from the reactor by means of expansion joint 24 lying within the intermediate chamber and the valve 27 is controlled to provide the desired flow rate irrespective of the position of the valve seat 28 in the end of the riser. It is preferred to supply from 10 to 40 per cent of the total amount of oxygen-containing regenerating gas through the riser and to convey the catalyst at from 10 to 60 ft. per sec. From 0.05 to 0.5 cu. ft. of said gas may be used in the riser per lb. of catalyst and 4 to 20 lb. per hour of catalyst per lb. of catalyst in the reactor may be carried up the riser. The catalyst passes into a distribution vessel 23 having small openings 34 in its convex upper surface. Regeneration gas is supplied through an annular pipe 36 also provided with openings, which surrounds the distributer. The regenerator generally contains 2 to 5 times as much material as the reactor and is of larger cross-section. Regeneration takes place at 700 DEG to 1200 DEG F., usually 1000 DEG to 1150 DEG F. with air. The catalyst passes after regeneration into the symmetrically placed standpipes 21 and 22 also equipped with expansion joints, which terminate preferably somewhat above the riser but sufficiently low to avoid immediate entry of the regenerated catalyst into the stripping zone, and are regulated by plug valves 29 and 30. Preferred sizes and proportions of apparatus are described. Reference has been directed by the Comptroller to Specification 767,769.
GB34928/54A 1953-12-14 1954-12-02 Improved method and apparatus for reacting carbon-containing gaseous compounds in the presence of a catalyst Expired GB788000A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US788000XA 1953-12-14 1953-12-14

Publications (1)

Publication Number Publication Date
GB788000A true GB788000A (en) 1957-12-18

Family

ID=22146298

Family Applications (1)

Application Number Title Priority Date Filing Date
GB34928/54A Expired GB788000A (en) 1953-12-14 1954-12-02 Improved method and apparatus for reacting carbon-containing gaseous compounds in the presence of a catalyst

Country Status (3)

Country Link
DE (1) DE1027827B (en)
FR (1) FR1117518A (en)
GB (1) GB788000A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1122649B (en) * 1959-01-15 1962-01-25 Kellogg M W Co Process and device for the conversion of hydrocarbons

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3492221A (en) * 1968-04-05 1970-01-27 Pullman Inc Apparatus and method for conversion of hydrocarbons

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2506307A (en) * 1941-12-30 1950-05-02 Standard Oil Dev Co Contacting gaseous fluids and solid particles
US2429721A (en) * 1944-01-28 1947-10-28 Standard Oil Dev Co Contacting gases and solids in fluidized systems
US2541077A (en) * 1949-01-29 1951-02-13 Universal Oil Prod Co Method and apparatus for contacting subdivided solid particles with a fluid reactantstream

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1122649B (en) * 1959-01-15 1962-01-25 Kellogg M W Co Process and device for the conversion of hydrocarbons

Also Published As

Publication number Publication date
DE1027827B (en) 1958-04-10
FR1117518A (en) 1956-05-23

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