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SECONDARY PROCESSING :
       Thermal conversion process




 THERMAL CONVERSION
        PROCESSES
• Thermal Cracking
• Visbreaking
• Coking
• Coke Calcination
• THERMAL CRACKING
    The processes is which hydrocarbons are decomposed
   at elevated temperatures to from material of lower Mol. wt.
   are called thermal conversion process. Any fraction of the
   crude from Naphtha to Vac. Residue – can be processed
   thermally.
    The most important types of thermal conversion process
   are thermal cracking, visbreaking and coking.
    Thermal cracking is used for conversion of residues and
   higher Mol. wt. hydrocarbons into more useful products by
   cracking the large hydrocarbon molecules into smaller ones
   at a temp. level of 4500 – 5000C.
    Cracking activity varies with the type of hydrocarbons
   and decrease in the following order:
   n–paraffin > Isoparaffins > cycloparaffins > aromatics >
   aromatics / naphthenics > polynuclear aromatics.
    Olefins crack to smaller olefins and di-olefins
     Important variables in thermal cracking are Temp.;
pressure and residence time.
 Cracking reactions begin to occur at Temp. of 315 – 3700C.
Pressure determines the phase in which the cracking
reactions take place. Thermal cracking conversion increases
with temp. and residence time.
 Under very severe thermal cracking conditions, there is
tendency for coke formation.
Cracking also generates double bonded hydrocarbons
(olefins). Side reactions like condensation and polymerization
reactions also occur leading to gum formation and tar-like
polymerization products. (To avoid this, gasoline or diesel
blend produced from thermal cracking process are
hydrotreated to make them stable usable product).
Since products of thermal cracking have very poor stability
and require further treatment ; Fluid catalytic cracking FCC
finds more favors with refiners.
• Simplified Thermal Cracking Process :
   Simple Thermal cracking process produces gas,
  naphtha, middle distillates and thermal tar from almost
  all variety of charge stocks from distillates to the
  heaviest crude and residual oils.

   The feed is heated to cracking temp. 4500 – 5000C
  and the cracked products containing gas and Full
  Boiling Range distillates enters the fractionators after
  passing through an intermediates separator vessel.
Gas+ gasoline


                                   F                  Gas oil
                       Cyclone     R
                                   A        Heavy Distillate
                                   C        + Recycle
Long                               T
                                   I
Residue                            O
                                   N
          Furnace                  A                  Furnace
                                   T
                                   O
                    Cracked        R

                    Residue
                              Cracked Residue
                                                         Gas+ Gasoline
                                   F
                                   R                     Gas Oil
                                   A
                                   C
                                   T
Short                              I
Residue                            O
                                   N
                                   A
          Furnace                  T
                                   O
                                   R
                                                     Cracked Residue
                         Thermal cracking process
 TYPICAL operating conditions and The Yield Patterns in The
SHELL process for Long Residue (Atmospheric Distillation column
bottoms) and Short Residue (Vacuum Distillation column bottoms)
are :
Cracking temperature, 0C            450 – 500
Furnace outlet pressure, kgf/cm2
(a) For residue                     4
(b) For heavy residue               20
Typical Yield Pattern
The yield of fractions in the Shell process for long residue and short
residue
                                               Yield, wt. % on feed
                                    Long residue                Short residue
                Products
                               (Two furnace operation)     (One furnace operation)



  C1 – C4                                4                            2
  C5 – 1650C                            8.5                           4
  165 – 3500C                           23.5                          12
• VISBREAKING

  Visbreaking – an abbreviation for viscosity breaking or
 viscosity lowering – is a liquid phase thermal conversion
 process to reduce the viscosity of Atmospheric (long
 reduce) and Vacuum (short residue) to produce
 specification fuel oil.
 Small quantities of LPG and a fair amount of naphtha are
 also produced.

  Visbreaking is a mild thermal cracking process and
 help in reducing the viscosities and pour point of long
 and short residues. Refinery production of heavy oils can
 be reduced by 30% using visbreaking. Visbreaking also
 produces gas, gas oil stock and gasoline which go for
 further processing.
 The principal reaction which occur during The Visbreaking are :
     Cracking of the side chains attached to cycloparaffins and
    aromatic rings.
     Cracking of resins to light hydrocarbons (primarily olefins)
     Some cracking of naphthene rings under higher temp.
       of operations (5000C)
 2. types of Visbreaking operations :
     Conventional Visbreaking (Furnace or coil cracking)
     Soaker Visbreaking
 Conventional Visbreaking :
       Also known as coil cracking, the process uses Furnace
outlet temp. of 475-5000C and reaction time from one to three
minutes. This process produces minimum of Naphtha and a
maximum of fuel oil from long and short residues and other
heavier feed stocks.
       Gas, Naphtha and light gas oils are recovered from the top
section of the fractionators. Gas and Naphtha can be further
processed in a gas concentration unit for the recovery of LPG.
Coil Visbreaker
                                                Gas




          Heater

                                             Gasoline
Reduced
Crude                                Steam
Charge                                       Gas Oil




                                               Tar
 Typical operating condition
       Equipment                      Operating parameter
       Furnace
       Furnace inlet temp. 0C                   3400C
       Furnace outlet temp. 0C             470 – 4900C
       Furnace inlet pres; kg/cm 2               22
       Furnace outlet pres; kg/cm 2              15
       Residence time ; minutes                  10
       Quench temp; 0C                          260
       Columns
                                      Fractionate        Stabilizer
       Top temp. 0C                      138                50
       Bottom temp 0C                    360                160
       Pressure kg/cm 2                   5.5               8.5
       Feed temp. 0C                       -                100
       Flash zone temp. 0C               395                 -
 Typical yield pattern


        Gas plus loss                 3

        Naphtha                       4

        Fuel oil (Visbroken         93*
        residue)

  *If  diesel production is to be maximized, a second
cracking furnace is added to the stream and the heavy
fraction boiling between 350 – 5000C, obtained by distilling
the visboken residue under vacuum is recycled to second
furnace for further cracking.
 Run lengths of 3 – 6 minutes are common for coil
visbreakers.
• Soaker Visbreaking :
 In this process a soaker drum is added between the
furnace and the fractionator. This drum provide large
residence time for the feedstock. The cracking reactions
take place in soaking drum. Since higher residence time
allows improved conversion at lower temps. ; Soaker
Visbreaking Technology is more energy efficient and
provides higher run lengths as coking reactions in the
furnace coil are significantly reduced. Run lengths to 6-18
months for Soaker Visbreaker.
 Other advantages of Soaker Visbreaking are :
 Lower capital cost (10/15% lower)
 Smaller furnace ; less waste Heat Recovery equipment
 Less pressure drop through furnace
 Lower fuel consumption (15% less fuel : 0.2% on feed)
 Better and more selective yields.
Gas
    Soaker Visbreaker




                                              Naphtha

                        Steam   Steam
                                               Gas Oil

               Soaker
               Drum
                                               Tar

      Heater

Residual
Stock
 Typical operating condition
         Equipment                   Operating parameter
         Soaker Drum
         Pre.                           5 – 15 bar (g)
         Temp.                             4400C
         Vapour Cracking                    minimum

         Liquid Cracking                    Yes
         Run length                       300 days


         Yield Pattern
         Product                        Yield; % of feed
         Gas                                 1.7
         Naphtha (80-2000C)                  3.1
         Light gas oil (200-3500C)          13.2
         Heavy gas oil (350-5200C)          27.0
         Residue (5200C+)                   55.0
 Visbreaking is an effective and cost – effective
way to produce more valuable products from heavy
residues. Earlier, it used to reduce the viscosity and/
or pour point of a fuel oil but now it is employed to
obtain Cat. Cracker feed and to reduce fuel oil
production.
• COKING
 Coking is the most widely practiced means of reducing
the C – H ratio of residual oils, Of the 2 main process –
delayed coking and fluid coking – more than 90% capacity is
in delayed coking units.
 Delayed coking is a thermal cracking process in which a
hydrocarbon feedstock, mainly residue is converted to lighter
and more valuable products and coke.
 Main advantage of the process is that it can take residual
stocks from a wide variety of process unit in a Refinery
Coking Furnace and the coke drums are the key elements in
the process. Cracking is initiated in the furnace tubes where
short residence time is allowed. Coking of the feed material
is delayed until it reaches large coking drums with larger
retention time; downstream of the coking heater.
 Three types of coke structures can be produced shot,
sponge or needle coke.
Decoking               Delayed Coking
Waterjet
                                                            Gas
                                              Accumulator
                                                      Naphtha
           Coke Drum                    P/A

                       Fractionator                   Steam Stripper

                                                            Steam


               Heater                                Light gas oil

                                                           Heavy
                                                  Steam
                                                           gas oil
                                              Steam Gen.


                                                            Feed
                  Condensate
                    Drum
    Coke
 Process Description

    • Delayed coking is a semi continuous process in which
    the heated charge is transferred to large coking drums
    which allow the long residence time needed to allow the
    cracking reactions to proceed to completion feed to
    these units is normally heavy atmospheric residues,
    although heavy catalytic cycle oils and cracked tars may
    also be used.

    • Feedstock gets pre heated by exchange of heat from
    outgoing products and is partially vaporized in a specially
    designed coking furnace. Mild cracking takes place in
    the furnace where thermal cracking temps; of 4850 to
    5050C are reached.
• From the furnace, the liquid-vapor mixture goes to the
coking drum (operating in batch-1 coking, the other
decoking). The vapors under-go cracking as they pass
through the coke drum.

•The cracked products go to fractionate where cracked
gas, Naphtha, Kerosene and gas oils are separated. The
petroleum coke is formed in the drum due to high
residence time of cracking in the drum.

• The feed stream is regularly switched between the
operating drum and drum under decoking. Decoking is
done using high pressure water jets. This generally fallows
a 12-16 hr. cycle.
 decoking operation

  Following procedure is used to remove the coke :

  (i) The coke deposit is cooled with water.
  (ii) One of the heads of the coking drums is removed
  to permit the drilling of a hole through centre of the
  deposit.
  (iii) A hydraulic cutting device, which uses multiple
  high pressure water jets, is inserted into the hole and
  the wet coke is removed from the drum.
  (iv) After the removal of coke from the coke drum, it is
  flushed with water and is readied for reuse.
• Typical operating conditions
             Furnace outlet temp.             4800 – 5150C
             Coke Drum Pressure               1.7 Kg/cm2g
             Fractionator top temp.           1500C
             Fractionator Bottom temp.        3500C
             Fractionator Pres.               1.4 – 3.4 Bar
                       Typical yield from delayed coker
             Feed
             0
                 API                     7.4          12.0    12.5
             Sulfur wt%                  2.76         1.6     0.6
             CCR wt %                    19.6         9.6     14.8
             Yields
             Gases                       13.2         12.0    6.4
             Naphtha                     11.1         15.7    21.6
             Light gas oil               31.4         35.2    46.0
             Heavy gas oil                -           15.5     -
             Coke                        44.3         21.6    26.0
             Sulfur in coke wt%          0.57         1.2     2.2
• Fluid Coking
     Fluid coking is a continuous process that uses the
    fluidized solids technique to convert residue including
    vacuum pitches to more valuable products.
     Fluid coking uses 2 vessels – a Reactor and a
    Burner. Both the reactor vessel and the burner vessel
    contain fluidized beds with coke particles circulating
    between the two vessel by fluidized solids technique.
    Coke particles are circulated to transfer heat to the
    reactor. The residuum is cooled by distributing it as a
    thin film of liquid on the outside of the hot-coke
    particles.
     The vapor products pass through cyclones that
    remove most of the entrained coke.
• COKE CALCINATION PROCESS
     Petroleum coke is produced as delayed sponge
    coke, delayed needle coke, fluid coke.
     Calcination of raw petroleum coke (green coke) is
    needed to transform it into useable material.
     Calcined coke is mostly used by the Aluminum
    Industry in the manufacture of anodes for Alumina
    Reduction, Calcined needle coke is used to
    manufacture. Graphite products and prebaked graphite
    electrodes for use in electro – metallurgical furnaces.
 • Process Description
  Calcination of green coke is essentially a high temp.
  treatment     involving    drying,    devolatilization    and
  dehydrogenation by which the C/H ratio of the feed is
  increased from about 20 to 1000. It may be carried out in a
  rotary kiln.
To Stock
                     Steam
                                 Green Coke



                                                              Fuel Gas
                   Incinerator            Rotary Kiln
                        &
                      Boiler


                                                        Rotary Cooler



    Coke Fines                                               Calcined
                                                               coke


                 Coke calcination process

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Thermal cracking (2)

  • 1. SECONDARY PROCESSING : Thermal conversion process THERMAL CONVERSION PROCESSES • Thermal Cracking • Visbreaking • Coking • Coke Calcination
  • 2. • THERMAL CRACKING  The processes is which hydrocarbons are decomposed at elevated temperatures to from material of lower Mol. wt. are called thermal conversion process. Any fraction of the crude from Naphtha to Vac. Residue – can be processed thermally.  The most important types of thermal conversion process are thermal cracking, visbreaking and coking.  Thermal cracking is used for conversion of residues and higher Mol. wt. hydrocarbons into more useful products by cracking the large hydrocarbon molecules into smaller ones at a temp. level of 4500 – 5000C.  Cracking activity varies with the type of hydrocarbons and decrease in the following order: n–paraffin > Isoparaffins > cycloparaffins > aromatics > aromatics / naphthenics > polynuclear aromatics.  Olefins crack to smaller olefins and di-olefins
  • 3. Important variables in thermal cracking are Temp.; pressure and residence time.  Cracking reactions begin to occur at Temp. of 315 – 3700C. Pressure determines the phase in which the cracking reactions take place. Thermal cracking conversion increases with temp. and residence time.  Under very severe thermal cracking conditions, there is tendency for coke formation. Cracking also generates double bonded hydrocarbons (olefins). Side reactions like condensation and polymerization reactions also occur leading to gum formation and tar-like polymerization products. (To avoid this, gasoline or diesel blend produced from thermal cracking process are hydrotreated to make them stable usable product). Since products of thermal cracking have very poor stability and require further treatment ; Fluid catalytic cracking FCC finds more favors with refiners.
  • 4. • Simplified Thermal Cracking Process :  Simple Thermal cracking process produces gas, naphtha, middle distillates and thermal tar from almost all variety of charge stocks from distillates to the heaviest crude and residual oils.  The feed is heated to cracking temp. 4500 – 5000C and the cracked products containing gas and Full Boiling Range distillates enters the fractionators after passing through an intermediates separator vessel.
  • 5. Gas+ gasoline F Gas oil Cyclone R A Heavy Distillate C + Recycle Long T I Residue O N Furnace A Furnace T O Cracked R Residue Cracked Residue Gas+ Gasoline F R Gas Oil A C T Short I Residue O N A Furnace T O R Cracked Residue Thermal cracking process
  • 6.  TYPICAL operating conditions and The Yield Patterns in The SHELL process for Long Residue (Atmospheric Distillation column bottoms) and Short Residue (Vacuum Distillation column bottoms) are : Cracking temperature, 0C 450 – 500 Furnace outlet pressure, kgf/cm2 (a) For residue 4 (b) For heavy residue 20 Typical Yield Pattern The yield of fractions in the Shell process for long residue and short residue Yield, wt. % on feed Long residue Short residue Products (Two furnace operation) (One furnace operation) C1 – C4 4 2 C5 – 1650C 8.5 4 165 – 3500C 23.5 12
  • 7. • VISBREAKING  Visbreaking – an abbreviation for viscosity breaking or viscosity lowering – is a liquid phase thermal conversion process to reduce the viscosity of Atmospheric (long reduce) and Vacuum (short residue) to produce specification fuel oil. Small quantities of LPG and a fair amount of naphtha are also produced.  Visbreaking is a mild thermal cracking process and help in reducing the viscosities and pour point of long and short residues. Refinery production of heavy oils can be reduced by 30% using visbreaking. Visbreaking also produces gas, gas oil stock and gasoline which go for further processing.
  • 8.  The principal reaction which occur during The Visbreaking are :  Cracking of the side chains attached to cycloparaffins and aromatic rings.  Cracking of resins to light hydrocarbons (primarily olefins)  Some cracking of naphthene rings under higher temp. of operations (5000C)  2. types of Visbreaking operations :  Conventional Visbreaking (Furnace or coil cracking)  Soaker Visbreaking  Conventional Visbreaking : Also known as coil cracking, the process uses Furnace outlet temp. of 475-5000C and reaction time from one to three minutes. This process produces minimum of Naphtha and a maximum of fuel oil from long and short residues and other heavier feed stocks. Gas, Naphtha and light gas oils are recovered from the top section of the fractionators. Gas and Naphtha can be further processed in a gas concentration unit for the recovery of LPG.
  • 9. Coil Visbreaker Gas Heater Gasoline Reduced Crude Steam Charge Gas Oil Tar
  • 10.  Typical operating condition Equipment Operating parameter Furnace Furnace inlet temp. 0C 3400C Furnace outlet temp. 0C 470 – 4900C Furnace inlet pres; kg/cm 2 22 Furnace outlet pres; kg/cm 2 15 Residence time ; minutes 10 Quench temp; 0C 260 Columns Fractionate Stabilizer Top temp. 0C 138 50 Bottom temp 0C 360 160 Pressure kg/cm 2 5.5 8.5 Feed temp. 0C - 100 Flash zone temp. 0C 395 -
  • 11.  Typical yield pattern Gas plus loss 3 Naphtha 4 Fuel oil (Visbroken 93* residue) *If diesel production is to be maximized, a second cracking furnace is added to the stream and the heavy fraction boiling between 350 – 5000C, obtained by distilling the visboken residue under vacuum is recycled to second furnace for further cracking.  Run lengths of 3 – 6 minutes are common for coil visbreakers.
  • 12. • Soaker Visbreaking :  In this process a soaker drum is added between the furnace and the fractionator. This drum provide large residence time for the feedstock. The cracking reactions take place in soaking drum. Since higher residence time allows improved conversion at lower temps. ; Soaker Visbreaking Technology is more energy efficient and provides higher run lengths as coking reactions in the furnace coil are significantly reduced. Run lengths to 6-18 months for Soaker Visbreaker.  Other advantages of Soaker Visbreaking are :  Lower capital cost (10/15% lower)  Smaller furnace ; less waste Heat Recovery equipment  Less pressure drop through furnace  Lower fuel consumption (15% less fuel : 0.2% on feed)  Better and more selective yields.
  • 13. Gas Soaker Visbreaker Naphtha Steam Steam Gas Oil Soaker Drum Tar Heater Residual Stock
  • 14.  Typical operating condition Equipment Operating parameter Soaker Drum Pre. 5 – 15 bar (g) Temp. 4400C Vapour Cracking minimum Liquid Cracking Yes Run length 300 days Yield Pattern Product Yield; % of feed Gas 1.7 Naphtha (80-2000C) 3.1 Light gas oil (200-3500C) 13.2 Heavy gas oil (350-5200C) 27.0 Residue (5200C+) 55.0
  • 15.  Visbreaking is an effective and cost – effective way to produce more valuable products from heavy residues. Earlier, it used to reduce the viscosity and/ or pour point of a fuel oil but now it is employed to obtain Cat. Cracker feed and to reduce fuel oil production.
  • 16. • COKING  Coking is the most widely practiced means of reducing the C – H ratio of residual oils, Of the 2 main process – delayed coking and fluid coking – more than 90% capacity is in delayed coking units.  Delayed coking is a thermal cracking process in which a hydrocarbon feedstock, mainly residue is converted to lighter and more valuable products and coke.  Main advantage of the process is that it can take residual stocks from a wide variety of process unit in a Refinery Coking Furnace and the coke drums are the key elements in the process. Cracking is initiated in the furnace tubes where short residence time is allowed. Coking of the feed material is delayed until it reaches large coking drums with larger retention time; downstream of the coking heater.  Three types of coke structures can be produced shot, sponge or needle coke.
  • 17. Decoking Delayed Coking Waterjet Gas Accumulator Naphtha Coke Drum P/A Fractionator Steam Stripper Steam Heater Light gas oil Heavy Steam gas oil Steam Gen. Feed Condensate Drum Coke
  • 18.  Process Description • Delayed coking is a semi continuous process in which the heated charge is transferred to large coking drums which allow the long residence time needed to allow the cracking reactions to proceed to completion feed to these units is normally heavy atmospheric residues, although heavy catalytic cycle oils and cracked tars may also be used. • Feedstock gets pre heated by exchange of heat from outgoing products and is partially vaporized in a specially designed coking furnace. Mild cracking takes place in the furnace where thermal cracking temps; of 4850 to 5050C are reached.
  • 19. • From the furnace, the liquid-vapor mixture goes to the coking drum (operating in batch-1 coking, the other decoking). The vapors under-go cracking as they pass through the coke drum. •The cracked products go to fractionate where cracked gas, Naphtha, Kerosene and gas oils are separated. The petroleum coke is formed in the drum due to high residence time of cracking in the drum. • The feed stream is regularly switched between the operating drum and drum under decoking. Decoking is done using high pressure water jets. This generally fallows a 12-16 hr. cycle.
  • 20.  decoking operation Following procedure is used to remove the coke : (i) The coke deposit is cooled with water. (ii) One of the heads of the coking drums is removed to permit the drilling of a hole through centre of the deposit. (iii) A hydraulic cutting device, which uses multiple high pressure water jets, is inserted into the hole and the wet coke is removed from the drum. (iv) After the removal of coke from the coke drum, it is flushed with water and is readied for reuse.
  • 21. • Typical operating conditions Furnace outlet temp. 4800 – 5150C Coke Drum Pressure 1.7 Kg/cm2g Fractionator top temp. 1500C Fractionator Bottom temp. 3500C Fractionator Pres. 1.4 – 3.4 Bar Typical yield from delayed coker Feed 0 API 7.4 12.0 12.5 Sulfur wt% 2.76 1.6 0.6 CCR wt % 19.6 9.6 14.8 Yields Gases 13.2 12.0 6.4 Naphtha 11.1 15.7 21.6 Light gas oil 31.4 35.2 46.0 Heavy gas oil - 15.5 - Coke 44.3 21.6 26.0 Sulfur in coke wt% 0.57 1.2 2.2
  • 22. • Fluid Coking  Fluid coking is a continuous process that uses the fluidized solids technique to convert residue including vacuum pitches to more valuable products.  Fluid coking uses 2 vessels – a Reactor and a Burner. Both the reactor vessel and the burner vessel contain fluidized beds with coke particles circulating between the two vessel by fluidized solids technique. Coke particles are circulated to transfer heat to the reactor. The residuum is cooled by distributing it as a thin film of liquid on the outside of the hot-coke particles.  The vapor products pass through cyclones that remove most of the entrained coke.
  • 23. • COKE CALCINATION PROCESS  Petroleum coke is produced as delayed sponge coke, delayed needle coke, fluid coke.  Calcination of raw petroleum coke (green coke) is needed to transform it into useable material.  Calcined coke is mostly used by the Aluminum Industry in the manufacture of anodes for Alumina Reduction, Calcined needle coke is used to manufacture. Graphite products and prebaked graphite electrodes for use in electro – metallurgical furnaces. • Process Description Calcination of green coke is essentially a high temp. treatment involving drying, devolatilization and dehydrogenation by which the C/H ratio of the feed is increased from about 20 to 1000. It may be carried out in a rotary kiln.
  • 24. To Stock Steam Green Coke Fuel Gas Incinerator Rotary Kiln & Boiler Rotary Cooler Coke Fines Calcined coke Coke calcination process