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Basic Training Kraft Process

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Page 1: Basic Concepts Kraft Process

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Basic Training

Kraft Process

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Wood

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Production of Chips

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Production of Chips

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Good Size of Chips

The size of the chips is very important for the impregnation of cook liquor (white liquor)

inside the chips.

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Selection of Chips

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Selection of chips

Mesh Discs

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Chip Bin

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Chip Bin Level ControlThe retention time is very important for the pre-heating of the

chips => take the air out of the chips for a good impregnation of 

the liquor inside the chips

a) Bad impregnation

b) Good impregnation

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Basic Concepts

• Kappa - Measurement of the delignification of 

the wood• Viscosity – Measurement of the quality of the

fiber. “Fiber length”

• White Liquor: NaOH+Na2S+Na2CO3

 –  Total Titratable Alkali (g/L): NaOH+Na2S+Na2CO3

 – Active Alkali (g/L): NaOH+Na2S

 –  Efective Alkali (g/L): NaOH+1/2Na2S

 –  Sulfidity (%) : Na2S/TTA

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Alkali Charge

• Alkali Charge: % of alkali (EA) added in the digester

relative to the wood. Alkali charge = 20% for

100 kg of wood is added 20 kg of alkali

• Kg of alkali / h = concentration of white liquor (EA)

(g/L or kg/m3) x flow of white liquor (m3 / h)• Kg of wood / h = chip meter (rpm) x 60 x vol of 

screw (m3) x chip density (kg/m3)

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Digester Production• Digester Production (adt/h) = chip meter

(rpm) x 60 x vol of screw (m3) x chip density(kg/m3) x yield / 0.9

• Adt – air dry ton – 10% of water

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Digester Retention Time• Retention time (min) = Volume of digester

(m3) * Compaction Factor (1.9)/ Chip meter(rpm) * volume of screw (m3)

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H Factor• Combination of time and temperature

• Temperature => Reaction rate

• Ex:

• Retention time = 1.5 h• Temperature = 170oC

How H Factor is calculated?

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H FactorReaction Rates (based on temperature) – Calculation of H Factor

H Factor = 921.4 (Reaction Rate 170oC) x 1.5 (Retention Time) = 1382

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H Factor

• H Factor = Retention Time (Hours) x Reaction

Rate for a given temperature (T)

• Reaction Rate = e^(43,2-16113/T)

• T – Temperature in Kelvin

RT (hours) 1,5

T(oC) 170

T(K) 443

RR 922,9172

H Factor 1384,376

Example

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Chip Meter

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Chip Meter

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Top Separator

Liquor and chips – Feed Circulation

Liquor – Feed Circulation - Return

Liquor and chips – Digester - Cooking

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Bottom of Digester

Importance of the cold

blow flow added at the

bottom of digester:

- Wash the pulp

- Controlling of blow

consistence

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Feed Circulation

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Digester

CD1 – Upper Extraction

CD3 – Lower Extraction

CD2 – Cook Circulation

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Digester Screens

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Brownstock Wash

DIG DDW DELIG SCREEN DDW BLEACHEVA

IndustrialWater

Filtrate

Tank

Filtrate

Tank

Weak

Liquor

TankLC

By passBy pass

Factors that affect BSW:

- High DDW Pressure / Low consistency in outlet

- High level of WLT / Low solids content in WL

Counter-current wash

Reuse of waterCOD

Condutivity

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Brownstock Wash

• Aims

 –  Clean the pulp

 –  Save water

 –  Recovery alkali

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Brownstock Wash

• Dirty pulp $$$

 –  Less efficiency in delignification process

 –  Greater consumption of chemicals in bleaching

• Water consumption $$$

 –  Greater consumption of steam in evaporation

• Recovery alkali $$$

 –  Less lost of soda

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Dilution Factor• Amount of wash liquor in excess in relation to

the dirty liquor mixed with the pulp• DF (m3/adt) = (Flow of wash liquor – liquor in the

pulp) (m3/h) /production (adt/h)

Ex1: –  Production = 100 adt/h

 –  Flow of wash liquor = 200 m3/h

 –  Liquor in the pulp = 100 m3/h –  DF = 1 m3/adt

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Dilution Factor• Ex2:

 –  Production = 100 adt/h

 –  Flow of wash liquor = 300 m3/h –  Liquor in the pulp = 100 m3/h

 –  DF = 2 m3/adt

• Ex3: –  Production = 100 adt/h

 –  Flow of wash liquor = 400 m3/h

 –  Liquor in the pulp = 100 m3/h –  DF = 3 m3/adt

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Dilution Factor• Conclusions

 –  DF = 1 2 x more wash liquor than dirty liquor in

pulp –  DF = 2 3 x more wash liquor than dirty liquor in

pulp

 – 

DF = 3

4 X more wash liquor than dirty liquor inpulp

 –  Can DF be 0 (zero) ?

• What does it mean ?

 –  Can DF be – (negative) ?• What does it mean ?

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Dilution Factor• DF = (Flow of wash liquor – liquor in the pulp) /production

• Flow of wash liquor is measured

• Production is measured

• How can be measured the amount of liquor in the pulp ? –  By the consistency!!!

• We have 2 ways of improving dilution factor: –  Increasing flow of wash liquor

 –  Increasing consistency in the outlet of the filter

• Same concept of wash and wring clothes!!!

  

   ∗

  

   −−

  

  = 9,01100Pr

WLof Flow

Out Consist oduction

 DF 

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Alkaline Loss

• The alkaline loss is usually measured after the lastDDW (before bleach process)

• It indicates the amount of soda (NaOH) presents inthe pulp that was “transfered” to the next process

• If this soda had been recovered with the washliquor it would go to recovery area and could berecovered

• The alkaline loss is an indirect measurent of thewashing process:

 –  High alkaline loss Bad wash

 –  Low alakline loss Good wash

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COD• Chemical oxygen demand – Indicates the

“dirt” rate of a pulp. It’s measured in lab. –  Pulp dirty High COD Bad wash

 –  Pulp clean Low COD Good wash

• In the process, the condutivity is as indirect

measurement of the COD

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O2 Delignification

NaOH or OWL

O2 MPS O2 MPS

Pulp

       R     e     a     c      t     o

     r       2

       R     e     a     c      t     o

     r       1

O2 Delignification

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O2 Delignification

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• Delignification efficiency: 30-40% –  Kappa in: 15-17

 –  Kappa out: 8-11

• It causes improvement on the brightness

• Filtrate free of ions Cl

• It isn't very selective. O2 attacks lignin and pulp.

• But it’s more selective than extend the cookingprocess until kappa 10 is reached in digester.

• If the process isn’t well controlled, viscosity canbe a problem!

O2 Delignification

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• Main variables of the process

 –  O2 Dosage: + 18 kg/adt

 –  Alkali Charge(15-20 kg/adt): Can be soda or oxidizedwhite liquor (OWL) or both. It’s important to thereaction, but in excess, can cause problems in theviscosity.

 – pH Control: + 11

 –  Temperature: High temperature is important to thedelignification kinetics, however, it could bedangerous to viscosity. About 100 oC.

 –  Pressure is very important to the delignificationkinetics

O2 Delignification

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Screening Process• Aims

 –  Take knots out –  Take shives out

 –  Take plastics out

 –  Take dirts out

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Screen

Feed

AcceptReject

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Screen

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Rotors

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Cylinder / Meshes

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Knot Separator Cilinder

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Mesh – Primary Screen

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Screens

Screen Process

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Screen Process

Feed

AccK

RejK

Knotter PrimaryAcc1

Rej1

Secondary

Acc2

Rej2

Tertiary

Acc3

Feed1

Feed2

Feed3

Rej3

Knot

Wash

Reject

WashDIG

DDW BLEACH

Screen Process

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Screen Process

BlowFlow

Pulp to Bleaching.

Knoter

Primary

Washer

Equipment

Knots to Digester

Fiber to blow tank

Knot Wash

Pressed

Reject

Bleaching

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g

Kappa Brite:

- Inlet of A Tower (Kappa & Brightness)

- Inlet of D0 (Kappa & Brightness)

- Outlet of EOP (Kappa & Brightness)

- Outlet of D1 (Brightness)- Outlet of P Bri htness

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Composition of Kappa #

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Bleaching – Why do use many stages?

Bleaching – 1 stage

BrightnessPulp Resistence

Chemical Charge Chemical Charge

Bleaching – Many stages

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Bleaching – Why do use many stages?

• Softer conditions

 – Lower temperature

 –  Less chemical charge

• Pulp is washed between stages (Filters /

Presses)

 –  Wash the pulp

 – 

Remove the lignin

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D Stage

• ClO2

• Oxidize and degrade the lignin• The lignin bocomes soluble

Selective – Little drop of the viscosity• D0 STAGE – Focus on removing the lignin

• D1 – D2 STAGE – Focus on bleaching the pulp

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E Stage

• Stage of extraction (of lignin)

• NaOH• Can be considered part of the previous stage

In this stage, the lignin that became soluble inD stage, is dissolved in the pulp and then it is

extracted

• Usually E stage is combined with O (oxygen)and P (peroxide)

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P Stage

• H2O2

• Focus on bleaching• Less selective than ClO2

A S

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A Stage

• Remove Hex,A

• High Temperature – 90 oC

• Dosification of H2SO4

• Low pH – 2,5 - 3

Long retention time: usually more than 3 hours• Main controls: pH and Temperature

• Kappa in: 10-11

Kappa out: 5-6• Brightness out: 60 – 65

D0

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Dosification of ClO2• Attack lignin and gain of brightness

• High Temperature – 90 oC

• pH – The same of A Stage – 

Low pH – 2,5 - 3• Short retention time: 20 minutes

• Main controls: ClO2 dosage and Temperature –  Kappa Factor Concept: Dosification based on kappa number

 – 

Conversion of ClO2 to Active Chlorine = 2,63 –  1 kg of ClO2 = 2,63 kg of Active Clorine

 –  Kappa Factor= 2 2 kg of active clorine per kappa # in the inlet of D0

• Common kappa factor= 2 – 3,5 (depends on the desired brightness in theoutlet of EOP)

• Kappa in: 5-6

• Kappa out: No measurement on line

• Brightness out: No measurement on line

• ClO2 at low pH – Good for remove lignin

EOP

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• Dosification of O2 and H2O2• In some plants – EP – There isn’t O2 dosification

• NaOH dosage is importante to increase pH

 –  6 – 8 kg of soda/adt

 –  pH: 10,5 – 11

• High pH is necessary to H2O2 develops his bleachingpower

• H2O2 dosage: 3 – 5 kg/adt

Retention time: 1,5 – 2 hours• Main controls: H2O2 dosage and pH

• Kappa out: 2 - 3

• Brightness out: 80 - 85

D1

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• Dosification of ClO2 (2 – 5 kg/adt)

• For controlling pH can be used NaOH or H2SO4

 – 

NaOH – pH: 5-5,5 – Good for gain brightness –  H2SO4 – pH: 2,5 – 3,5 – Good for delignification (in case

of problems with shives)

• Retention time: 1,5 – 2 hours• Main controls: ClO2 dosage and pH

Kappa out: (very low)• Brightness out: 86 - 90

P

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• Dosification of H2O2 (3kg/adt)

• For controlling pH is used NaOH

 – 

2,5-4 kg NaOH/adt –  pH: 10,5 - 11

• Retention time: 1,5 – 2 hours

• Main controls: H2O2 dosage and pH

• Kappa out: (very low)

• Brightness out: 89 - 93

Calculation of Total Active Chlorine

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Calculation of Total Active Chlorine

• ClO2 – 2.63

• H2O2 – 2.09• TAC (kg/atd) = ClO2 dosage x 2.63 + H2O2

dosage x 2.09

Brightness Reversion

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Brightness Reversion

• Sources of brightness rerversion

 – 

Wrong pH in the process –  Lignin

 –  Extractives

 –  Hexenuronic Acid

Importance of last stage = P

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Importance of last stage = P

0.5

1

1.5

2

2.5

3

3.5

4 D(PO)DD

DHT(PO)DD

 A/D(PO)DD

   R

   e   v   e   r   s   i   o   n

 ,   %   I   S   O

D(PO)DP

DHT(PO)DP  A/D(PO)DP

Avoiding Brightness Reversion

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Avoiding Brightness Reversion

• Remove the lignin

• Minimizing HexA’s• Final kappa # < 1

Finish the bleaching sequence in P• Final pH (after dried) > 7

Recovery Cycle

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Ca

Cycle Na

Cycle

Evaporation

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Weak Liquor Concentration: 14-20%Strong Liquor Concentration: Aprox. 80%

Vacuum

Evaporation

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Evaporation

1 – Live Steam

2 - Condensed

3 – Diluted Liquor

4 – Concentrated Liquor

5 - Evaporated

“ The evaporated of one effect is condensed in the next effect”

Recovery Boiler

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Causticizing

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Causticizing

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Causticizing

• Green Liquor => H2O + Na2CO3 + Na2S

•Slaking Reaction (Exotermic Reaction) –  CaO + H2O (green liquor) -> Ca(OH)2

• Causticizing Reaction (Equilibrium Reaction)

 –  Ca(OH)2 + Na2CO3 (green liquor) 2 Na(OH)

(white liquor) + CaCO3 (lime mud)

Calcination Reaction –  CaCO3 + heat -> CaO + CO2

• White Liquor => NaOH + Na2S + Na2CO3

Lime Cycle

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Lime Cycle