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Process and apparatus for fluid bed catalytic cracking

  • US 4,695,370 A
  • Filed: 08/02/1985
  • Issued: 09/22/1987
  • Est. Priority Date: 08/02/1984
  • Status: Expired due to Term
First Claim
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1. A process for catalytically cracking a liquid hydrocarbon charge in a fluidized bed reaction zone having an upper and lower part wherein the charge and the catalyst flow co-currently in a downward direction, and for regenerating the catalyst in first and second regeneration zones, said process comprising:

  • injecting the liquid charge at the upper part of the reaction zone through at least one line which is subdivided into a plurality of substantially vertical first ducts with each of said first ducts being provided at its lower end with spray means for dispensing the liquid charge as droplets, introducing into an enclosure located within the upper part of the reaction zone catalyst particles having a temperature which is in a range from 600°

    to 950°

    C., the catalyst particles being introduced through at least one second duct into the enclosure so as to define a catalyst fluidized bed in said enclosure,circulating a gas through said fluidized bed so as to downwardly drive the catalyst particles of the fluidized bed through a plurality of substantially vertical third ducts thereby introducing the catalyst particles into the reaction zone itself, each vertical first duct being coaxial with one of the third ducts, each means for spraying the liquid charge being juxtaposed with an upper end of said third duct, so as to obtain in said third duct a flow of liquid charge and entrained catalyst particles in order to completely vaporize the liquid charge and intimately admix the charge with the catalyst particles,maintaining contact in said reaction zone between the liquid charge and the catalyst, with a residence time of the charge from 0.1 to 10 seconds and at a temperature in the range of 450°

    -700°

    C. to produce a reaction effluent stream,increasing the velocity of the catalyst and the reaction effluent in the lower part of the reaction zone, said lower part being funnel shaped and convergingdownwardly at a half apex angle ranging from about 5 to 30°

    ,separating 50 to 90% of the catalyst particles from the reaction effluent stream in a generated spiral within at least one first separation zone having an inlet and outlet and having a residence time lower than one second, the velocity of the gaseous portion of the reaction effluent at the inlet of said first separation zone being from 10 to 40 meters per second so as to produce a helical flow of vapor without reversal of the generated spiral, with the major part of the remaining catalyst particles being driven along with the gaseous effluent and then being separated from the reaction effluent within at least one second separation zone which includes the reversal of a spiral stream generated by the injection of the gaseous flow into said second separation zone,removing the major part of the hydrocarbons from the catalyst particles by the introduction of a stripping gas,conveying the catalyst particles upwardly through a fourth duct to a first fluidized bed regeneration zone by means of a first carrier gas,performing a first catalyst regeneration step, within said first regeneration zone at a temperature T1 ranging from about 500°

    to 750°

    C., with a fluidizing gas which comprises oxygen or a molecular oxygen-containing gas, so as to cause the combustion of at least 90% of the hydrogen and so as to oxidize 10-60% by weight of the carbon present on the catalyst,removing the major part of the gases from the first regeneration zone,withdrawing the partially regenerated catalyst from said first regeneration zone, feeding it upwardly through a first transfer line, by means of a second carrier gas comprising a molecular oxygen-containing gas to a lower part of a second regeneration zone, the second regeneration zone having the shape of a substantially vertical and elongate tube having a length L, and diameter φ

    , whose ratio L/O ranges from 3 to 90, the catalyst being further regenerated in the second regeneration zone by being treated with the second carrier gas at temperature T2 from 650°

    to 1000°

    C., with T2 being higher than T1, in order to obtain a regenerated catalyst containing no more than 0.04% by weight of coke, the catalyst having this been driven upwardly through the second regeneration zone by means of said second carrier gas, andwithdrawing from the second regeneration zone a gas-catalyst mixture, separating the catalyst particles from the gases and feeding these regenerated particles, which have a temperature from 600°

    to 950°

    C., into said at least one second duct.

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