γδ δΝδ             ΡΗΣαδν                 ΓεΟΗέδΗ               ΗαΡΖνΣνΙ

 

7- Catalytic Cracking

  1. Purpose:

to increase the octane # of gasoline, while maintaining yield from high-boiling stocks using catalysts.

 

  1. History of Catalytic cracking

1). Batch reactor catalytic cracking to produce light distillates (1915)

•         Catalyst: AlCl3 - A Lewis acid, electron acceptor

             Alkane - electron (abstracted by AlCl3 )-> a carbocation(+)

                        -> ionic chain reactions to crack long chains

2).Houdry (1936) - a commercial process

•         Continuous feedstock flow with multiple fixed-bed reactors

Cracking/catalyst regeneration cycles

•         Catalyst: clays, natural alumina/silica particles

3). Thermoform Catalytic Cracking (TCC) (1942)

•         Continuous feedstock flow with moving-bed catalysts

•         Catalyst: synthetic alumina/silica particles

•         Higher thermal efficiency by process integration

4). Fluid Catalytic Cracking (FCC) (1942)

•         Continuous feedstock flow with fluidized-bed catalysts

•         Catalyst: synthetic alumina/silica +zeolites (1965)

    4. Process diagram

5. Feedstock and Products

Feedstocks:

•          straight – run gas oil

•          vacuum gas oil

•          atmospheric residue

•          heavy ends (coker gas oil, DAO)

•          vacuum residue        

Pretreatment:

•          deasphalting – to prevent excessive coking on catalyst surfaces

•          demetallation (Ni, V) – prevent catalyst deactivation

•          hydrocracking – to prevent excessive coking        

 

Products from Catalytic Cracking

n-paraffins, i-paraffins, aromatics, naphthenes, and olefins. I-paraffins come from ionic reaction, is branchesd chain, have high Oct.#

C3 – C4 gases

C5 – C10 isoparaffins (gasoline), olefins, aromatics, napthenes

> C10 – light cycle oil

> C14 – decant oil

6. Comparison between thermal and catalytic cracking

 Catalytic cracking is differences wrt Thermal Cracking

•          uses a catalyst

•          lower temperature

•          lower pressure

•          more flexible

•          different reaction mechanisms

-         ionic vs. free radical

•         High thermal efficiency

•         Good integration of cracking and regeneration

•         High yields of gasoline and other distillates

•         Low gas yields

•         High product selectivity

•         Low n-alkane yields

•         High octane number

•         Chain-branching and high yield of C4 olefins

•         High yields of aromatics

 

 

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