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E&C Cry og en i cs Standard P lan ts
Nitrogen Generation Unit APSA L1)Training documentation
Peru LNG
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Generic part1
stDay
Welcoming introduction
Process introduction
Summary and training program philosophy
Nitrogen Generation Unit systemic presentation
PFD & PID
Compression modulePurification module
2sd
Day
Heat Exchange module
Distillation module
Cold Production module
Mass balance
Safety : CnHm risks, safely operation
Operation training3rd Day
Process control overview
Start-up and shutdowns
Deriming / Drying & exceptional regeneration
Main control loops
Alarms and trips
Operating manual
R01/R02 timing
Supervision in steady conditions
Trouble shooting
quiz Operators questions and answers
Taining - PERU LNGNitrogen Generation Uni t
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PRESENTATIONPRESENTATIONPRESENTATION
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1. Generalities
1.1. Nitrogen On-Site Supply System
N2 Production (Nm3/h)
Bulk SupplyBulk Supply
10100 1000 10000
100%
99.9%
95%
SPISPISmall MembranesSmall Membranes
AMSAAMSALarge MembranesLarge Membranes
APSA LAPSA L
APSA LEAPSA LELargeLarge CryoCryo..
High PurityHigh Purity
LINLIN
APSAAPSASmallSmall CryoCryo..
N2 purity
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1. Generalities
1.2. APSA L /LE : Process and Markets
ChemicalsChemicals
RefineriesRefineriesGlassGlass
APSAAPSA--LL
GlassGlassAPSAAPSA--LCLC
APSAAPSA--LELE ElectronicsElectronics
Classic
7-10 barA N2
Claude Cycle
2-3 barA N2
Booster Re-cycle
Ultra High Purity
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1. Generalities
1.3. Air Separation Unit (ASU) Inlet & Outlet
Air
SeparationUnit
PRODUCTS:
O2, N2, Ar(gas or liquid)
SOURCE :
Atmospheric Air
WASTE NITROGEN
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1. Generalities
1.4. Raw material composition
OXYGENNITROGENARGON
HELIUMNEON
KRYPTONXENON
HYDROGENSTEAM
CARBON DIOXIDE
HYDROCARBONS {
O2N2Ar
HeNeKrXeH2
H2O
CO2CH4
20,9 %78,1 %0,93 %
5,24 ppm18,18 ppm1,139 ppm0,086 ppm0,5 ppm
variable300 700 ppm
3 5 ppm
ELEMENTS SYMBOLCOMPOSITION
IN VOLUME
< 0.5 ppmC2+
Principal
Rare gas
Impurities
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1. Generalities
1.5. Cryogenic production stages ?
DISTILLATIONCOMPRESSION
PURIFICATION
HEAT
EXCHANGE
COLD
PRODUCTION
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1. Generalities
1.6. Cryogenic production modular approach
COMPRESSION
PURIFICATION
HEAT
EXCHANGE
DISTILLATION
COLD
PRODUCTIONResidual Gas
GASEOUS
PRODUCTS
LIQUID
PRODUCTS
Air
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1. Generalities
1.7. Plants Modules Overview
COMPRESSION
PURIFICATION
COLD PRODUCTION
HEAT
EXCHANGE
DISTILLATION
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1. Generalities
1.8. APSA L : Global Scheme
Nitrogen recoveryNitrogen recovery 40%40%
APSA LAPSA L
GANGAN
Residual GasResidual Gas
AIRAIR
LINLIN
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1. Generalities
1.9. APSA L : Process Cycle
Gaseous N2to customer
Liquid N2to backup
Residual Enriched Gas (>35% O2)
Cooling WaterPower Civil Works
R01 R02
D01
Compression Purification Cold Production Heat Exchange Distil lation
Air
inlet
C01
K01
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AIR PURIFICATIONAIR PURIFICATIONAIR PURIFICATION
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TO REMOVE THE VARIOUS AIR CONTAMINANTS IN ORDER TOPREVENT TROUBLES IN APSA UNITS:
TEMPERATURE ~ -180C
TO REMOVE THE VARIOUS AIR CONTAMINANTS IN ORDER TOPREVENT TROUBLES IN APSA UNITS:
TEMPERATURE ~ -180C
WATER (air moisture)WATER (air moisture)
Carbon Dioxide CO2Carbon Dioxide CO2
Hydrocarbons CnHmHydrocarbons CnHm
Nitrous oxide (N2O)Nitrous oxide (N2O)
Air Purification OBJECTIVESOBJECTIVESOBJECTIVES
Ai P ifi i
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Purification requirementsPurificationPurification requirementsrequirements
- unit corrosion
- plugging (pipes, exchangers, column) by solidification
due to cryogenic temperature (0C / ice)
- unit corrosion
- plugging (pipes, exchangers, column) by solidification
due to cryogenic temperature (0C / ice)
WATER
- plugging (pipes, exchangers, column) by solidif ication
due to cryogenic temperature (-130C / solid CO2)
- plugging (pipes, exchangers, column) by solidification
due to cryogenic temperature (-130C / solid CO2)
O
- explosion r isk in the vaporizers with oxygen enrichedatmosphere (Rich Liquid, Oxygen)
- explosion risk in the vaporizers with oxygen enrichedatmosphere (Rich Liquid, Oxygen)
nHm
- explosion risk with CnHm- explosion risk with CnHm O
Air Purification
Ai P ifi ti
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Air CompositionAir Composition Inlet Comp.Inlet Comp. Inlet Comp.Inlet Comp. PurifPurif. Outlet. Outlet
NormalNormal PeakPeak MaxMax allowaballowab
N2 Nitrogen 78.11 %O2 Oxygen 20.96 %
Ar Argon 0.93 %
H2O Water saturation
CO2 Carbon Dioxide 350 450 ppm 600 ppm 0.1 ppmCnHm Hydrocarbons < 0.1 ppm 0.5 ppm
Ne Neon 18 ppm
He Helium 5.2 ppm
CH4 Methane 1 6 ppm 15 ppm 8 ppmKr Krypton 1.139 ppm
H2 Hydrogen 0.5 ppm
Xe Xenon 0.086 ppm
+ other natural or industr ial impurities : hydrocarbons,CO, H+ other natural or industrial impurities : hydrocarbons,CO, H22S, NOS, NO22 ..........
Air Composition / Air ContaminantsAir Composition / Air ContaminantsAir Composition / Air Contaminants
Air Purification
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Contaminant-free
Air
Air with
contaminants:
H2O, CO2,CnHm
OBJECTIVES:
ELIMINATION OF WATER IN VAPOUR FORM
ELIMINATION OF CARBON DIOXIDE CO2
ELIMINATION OF HYDROCARBONS EXCEPTMETHANE CH4 and some other CnHm
OBJECTIVES:
ELIMINATION OF WATER IN VAPOUR FORM
ELIMINATION OF CARBON DIOXIDE CO2
ELIMINATION OF HYDROCARBONS EXCEPTMETHANE CH4 and some other CnHm
Air passes through upward a vesselequipped with two specific materials:
-ALUMINA: to trap water molecules
- MOLECULAR SIEVE: to trap CO2 and
Hydrocarbon molecules
Air passes through upward a vessel
equipped with two specific materials:
-ALUMINA: to trap water molecules
- MOLECULAR SIEVE: to trap CO2 and
Hydrocarbon molecules
ALUMINA:
WATER
MOLECULAR
SIEVE:
CO2, CnHm
Process presentationProcessProcess presentationpresentationAir Purification
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TheADSORPTION process occurs
in 2 steps:
- first, an attraction of the
molecules to the adsorbent
- then, a diffusion of the
molecules into the pores where
they are fixed (or trapped).
TheADSORPTION process occurs
in 2 steps:
- first , an attraction of the
molecules to the adsorbent
- then, a diffusion of the
molecules into the pores where
they are fixed (or trapped).Adsorbent
Pores
ATTRACTION
DIFFUSION/
FIXATION
Molecules
ALUMINA and MOLECULAR SIEVE
are solid materials in the form ofporous particles of 2 to 5 mm
diameter: they are called
ADSORBENTS.
ALUMINA and MOLECULAR SIEVE
are solid materials in the form of
porous particles of 2 to 5 mm
diameter: they are called
ADSORBENTS.
Adsorption ProcessAdsorptionAdsorption ProcessProcessAir Purification
Air Purification
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Reversible Process : Adsorption & Desorption
Adsorption increases (the amount of
adsorbed molecules increases) when:
the pressure increases
the temperature decreases
Adsorption increases (the amount of
adsorbed molecules increases) when:
the pressure increases
the temperature decreases
ADSORPTION IS A REVERSIBLE PROCESS:
if the pressure decreases or if the temperature increases, theadsorbed molecules will be able to leave the pores of the adsorbentparticles: this is the Desorption of the adsorbent.
(also called Regeneration)
ADSORPTION IS A REVERSIBLE PROCESS:
if the pressure decreases or if the temperature increases, theadsorbed molecules will be able to leave the pores of the adsorbentparticles: this is the Desorption of the adsorbent.
(also called Regeneration)
Thus, for a fixed adsorbent quantity, we design a cyclic processwith alternating phases: adsorption/desorption.
we can play with the temperature: TSA cycle (TemperatureSwing Adsorption)
we can play with the pressure: PSA cycle (Pressure SwingAdsorption).
Thus, for a fixed adsorbent quantity, we design a cyclic processwith alternating phases: adsorption/desorption.
we can play with the temperature: TSA cycle (TemperatureSwing Adsorption)
we can play with the pressure: PSA cycle (Pressure SwingAdsorption).
AdsorbedAdsorbedphasephase
GaseousGaseousphasephase
SolidSolid
Adsorption ProcessAdsorptionAdsorption ProcessProcessAir Purification
Air Purification
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The name of Adsorbents designates porous solid materials.
Their main characteristic is a maximum surface (active zone for the adsorptionprocess) in a small
volume: we define the specific area.
Adsorbents come in different forms:- spherical balls- cylindrical pellets- irregular crushed particles
Chimical
formula
Specific
area
m2/g
Pore diameter
Angstrm
(10-10
m)
ACTIVATEDCARBON
C 800 to 1500 40 to 5000
ALUMINA AL2O3 300 to 350 10 to 40
MOLECULAR
SIEVE:
Type A, Type X
SiO2, Na2OCaO, K2O
900 3 to 10
Each gram of product
particle has a surface
equivalent to a tennis
court
Adsorbent characteristicsAdsorbentAdsorbent characteristicscharacteristicsAir Purification
S fAir Purification
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Affinity (Adsorbent / Molecule) depends on :
The type of adsorbent: presence of attraction field diameter of the pores
The type of adsorbent:presence of attraction fielddiameter of the pores
The type of molecule: their physical and chemical characteristics determine the intensity of the
adsorbent attraction: so, we designate
molecules strongly attracted (with electrical moment)and molecules weakly attracted (neutral molecules) the size of the molecules must be smaller than the diameter of the pores:
thus, nitrogen molecule is able to pass into a 4 pore, but not into a 3 pore.
The type of molecule:their physical and chemical characteristics determine the intensity of the
adsorbent attraction: so, we designatemolecules strongly attracted (with electrical moment)and molecules weakly attracted (neutral molecules)
the size of the molecules must be smaller than the diameter of the pores:thus, nitrogen molecule is able to pass into a 4 pore, but not into a 3 pore.
Adsorbed molecules
ACTIVATED CARBONOil vapour:
Hydrocarbons C2 and C3 typesALUMINA H2O
MOLECULAR
SIEVE
C2H2, NO2, CO2, H20
Selectivity of the processSelectivitySelectivity of theof the processprocessAir Purification
Ch iCh i ff d bd b tAir Purification
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The function of the adsorption process for an APSA unit is to trap in vapour form
the air contaminants such as water, carbon dioxide CO2 and hydrocarbons, beforefeeding the cold box.
To trap water, knowing that air is always saturated after compression process, thechoice indifferently could be molecular sieve or alumina.
We prefer alumina for the following reasons:
- alumina is less sensitive to the possible presence of liquid water particles- the temperature of regeneration process for alumina is colder:
around 40C for alumina, 250C for molecular sieve
To trap CO2, the only choice is molecular sieve.
The same for hydrocarbons, mainly made up of acetylene C2H2:it is not possible to trap methane CH4 by the adsorption process.
MOLECULAR SIEVECO2, C2H2
MOLECULAR SIEVECO2, C2H2
ALUMINAH2O
ALUMINAH2O
Choice of adsorbentsChoiceChoice ofof adsorbentsadsorbentsAir Purification
Ad ti W tAd ti W t llAir Purification
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Saturated zone front Clean zone
ADSORPTION
DESORPTION (REGENERATION)
END OF DESORPTION (REGENERATION)
Dry gas
Saturated Gas
Saturated Gas Dry gas
Adsorption: Water analogyAdsorption: WaterAdsorption: Water analogyanalogyAir Purification
I t ll ti d iI t ll ti d iI t ll ti d iAir Purification
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The design of the installation is a combination with two types of adsorbents:
first , compressed air passes through a bed of alumina in order to trap water
then, compressed air passes through a bed of molecular sieve intended to trapCO2 and Hydrocarbons
Thus, we keep molecular sieve free of moisture contamination.
The design of the installation is a combination with two types of adsorbents:
first, compressed air passes through a bed of alumina in order to trap water
then, compressed air passes through a bed of molecular sieve intended to trapCO2 and Hydrocarbons
Thus, we keep molecular sieve free of moisture contamination.
AIR
MOLECULAR SIEVECO2, C2H2
ALUMINAH2O
AIR
Adsorber
V-6701 A/BALUMINA
MOLECULAR
SIEVE
Installation designInstallation designInstallation designAir Purification
Ad ti / R ti C lAdsorption / Regeneration CycleAdsorption / Regeneration CycleAir Purification
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Using a fixed amount of adsorbent, we know that the duration of adsorption process will be limited:
after a certain duration of air circulation, the pores of the adsorbent become saturated:- with water molecules for alumina- with CO2 and Hydrocarbon molecules for molecular sieve
We obtain the saturation of the adsorbents: the adsorption process is
over.
Using a fixed amount of adsorbent, we know that the duration of adsorption process will be limited:
after a certain duration of air circulation, the pores of the adsorbent become saturated:- with water molecules for alumina- with CO2 and Hydrocarbon molecules for molecular sieve
We obtain the saturation of the adsorbents: the adsorption process is
over.
To achieve a continuous air purification
compatible with the non-stop distillationprocess of APSA unit, we need an
operating cycle with two adsorbers.
An arrangement with two adsorbers in parallelallows to purify compressed air with one adsorber
(ADSORPTION phase), while the second one is indesorption process (REGENERATION phase).
When the first adsorber is close to the limit ofadsorption capacity, we perform a reverse
operation in order to feed with compressed air the
second adsorber, which is contaminant-free thanksto the previous regeneration process.
To achieve a continuous air purif ication
compatible with the non-stop disti llationprocess of APSA unit, we need an
operating cycle with two adsorbers.
An arrangement with two adsorbers in parallelallows to purify compressed air with one adsorber
(ADSORPTION phase), while the second one is indesorption process (REGENERATION phase).
When the first adsorber is close to the limit ofadsorption capacity, we perform a reverse
operation in order to feed with compressed air the
second adsorber, which is contaminant-free thanksto the previous regeneration process.
Contaminant-free
air
Air with
contaminants
ADSORPTION
Adsorption / Regeneration CycleAdsorption / Regeneration CycleAdsorption / Regeneration CycleAir Purification
REGENERATION
Ad ti f t i th b dAdsorption front in the bedAdsorption front in the bedAir Purification
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0100200300400500
0
0 1 2 3 4 5
CO2 (ppm) Adsorbed quantity
Bed
Height
t = 100 min
t = 20 min
Adsorbed
quantity
Adsorption front in the bedAdsorption front in the bedAdsorption front in the bedAir Purification
Air wi th contaminants
Contaminant-free
air
Regeneration front in the bedRegeneration front in the bedRegeneration front in the bedAir Purification
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CO2 (ppm) Desorbed quantity
Bed
He
ight
Saturated Vaporized
Rich Liquid
Vaporized
Rich Liquid
0100200300400500
0
0 1 2 3 4 5
Desorbed
quantity
Regeneration front in the bedRegeneration front in the bedRegeneration front in the bedAir Purification
Regeneration fluid : Vaporized Rich Liquid (VRL)
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Air Purification TechnologyTechnologyTechnology
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Horizontal beds
Adsorption phase :
Cycle time : 150 min
Air pressure : 8.1 bar g Air temperature : 40C
Regeneration phase :
Regeneration temperature : 90C
(heater outlet) Air pressure : 0.1 bar g
Heating duration : ~20 min
Cooling duration : ~100 min
Horizontal beds
Adsorption phase :
Cycle time : 150 min
Air pressure : 8.1 bar g Air temperature : 40C
Regeneration phase :
Regeneration temperature : 90C
(heater outlet) Air pressure : 0.1 bar g
Heating duration : ~20 min
Cooling duration : ~100 min
Mole Sieve bed
Alumina bed
Air
VaporizedRich Liquid
Air
TechnologyTechnologyTechnology
Vaporized
Rich Liquid
Regeneration fluid : Vaporized Rich Liquid (VRL)Regeneration fluid : Vaporized Rich Liquid (VRL)
Air Purification V01 / V02 InstallationV01 / V02 InstallationV01 / V02 Installation
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VRL Air to Cold Box
Event
Air
V-6701A
V-6701B
Electr ic heater EH-6701
AdsorptionPhase
RegenerationPhase
CVAG06B
KV 530
CVAG06A
CVWO009BCVWO009A
KV 525KV 515
KV 520KV 510
KV 516 KV 526
V01 / V02 InstallationV01 / V02 InstallationV01 / V02 Installation
VRL
Air Purification Purification cyclePurification cyclePurification cycle
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Purification steps
HP Isolation
Depressurization
Blow-Off
Heating
Cooling
LP Isolation
Pressurization
Parallel position
Adsorption
Purification cyclePurification cyclePurification cycle
Air
VRL
Air
Bottle in
Adsorption
phase
VRL
Bottle in
Regeneration
phase
Air Purification Pressure cyclePressure cyclePressure cycle
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Pressure cyclePressure cyclePressure cycle
Air
VRL
Air
Bottle in
Adsorption
phase
VRL
Bottle in
Regeneration
phase
Bott le 1
Bott le 2
time
press
ure
time
Heating Cooling
Heating Cooling
pres
sure
Adsorption
Adsorption
Regeneration
Regeneration
Air Purification Automatic sequenceAutomatic sequenceAutomatic sequence
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On line V6701 B
HP Isolation V6701 A
VRL Cold Box
Event
Air
V6701
A
V6701
B
Depressurization V6701 A
VRL Cold Box
Event
Air
V6701
A
V6701
B
Automatic sequenceAutomatic sequenceAutomatic sequence
Air Purification Automatic sequenceAutomatic sequenceAutomatic sequence
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VRL Cold Box
Event
Air
V6701
A
V6701
B
Heating V6701 ABlow-Off V6701 A
VRL Cold Box
Event
Air
V6701
A
V6701
B
Automatic sequenceAutomatic sequenceq
Air Purification Automatic sequenceAutomatic sequenceAutomatic sequence
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Air
VRL Cold Box
Event
V6701
A
V6701
B
LP Isolation V6701 ACooling V6701 A
VRL Cold Box
Event
Air
V6701
A
V6701
B
Automatic sequenceqq
Air Purification Automatic sequenceAutomatic sequenceAutomatic sequence
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Parallel PositionPressurization V6701 A
VRL Cold Box
Event
Air
V6701
A
V6701
B
VRL Cold Box
Event
Air
V6701
A
V6701
B
uto at c seque ceqq
Air Purification Temperature profileTemperature profileTemperature profile
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GoodRegeneration
indicator
Time
Temperature
Heating Cooling
Inlettemperature
Outlet
temperatureCold Desorption Hot Desorpt ion
Heat Peak
Heating temperature
VRL temperature
at cold box outlet
p pp pp p
Air Purification
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What does the purif ication process look like ?
Air Purification
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What does the purif ication process look like ?
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EXCHANGERSEXCHANGERSEXCHANGERS
4. Heat Exchange
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4.1. Why exchange the heat ?
Gaseous N2to customer
Liquid N2to backup
Residual Enriched Gas (>35% O2
)
R01 R02
D01
Compression Purification Cold Production Heat Exchange
Distillation
Air
inlet
C01 K01
CRYOGENICCRYOGENICNONNON--CRYOGENICCRYOGENIC
4. Heat Exchange
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4.2. Principles of Heat Exchange
GOAL
To get air at good conditions for the distillation
To warm up gaseous product from the cryogenictemperature to the ambient one
PRINCIPLESHeat flux from the Hot fluid to cold fluid
Driving force = temperature difference
Counter flow arrangement
Heat exchange in an aluminium brazed Heat Exchanger
4. Heat Exchange
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4.3. Heat exchange formula
where
H = Duty or Heat exchanged (kcal/h)K = Heat exchange coeff
= f(fluids, material, flow) (kcal/h.m2.C)
S = Surface (m2)
T = Average temperature difference between hot
and cold f luids (C)
H = K . S
. Ln(T)
4. Heat Exchange
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4.4. Heat exchange formula
H = Q . Cp
. T
where
H = Duty or Heat exchanged (kcal/h)Q = Flowrate
(Nm3/h)
Cp = Specific heat (kcal/Nm3/C)
T = Temperature difference for the same fluid (C)
4. Heat Exchange
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4.5.Three types of heat exchanger
Cross currentCross current
++
++
CounterCounter--currentcurrent CoCo--currentcurrent
++
4. Heat Exchange
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4.6. Co-current exchanger
Insulation
-100C
0C
-100C
-50C
-50C
-50C
Cold Nitrogen
Cold Nitrogen
Hot Nitrogen
Same number of hot passages and cold passages
Temperature of Hot Nitrogen at the end of the exchanger ?
4. Heat Exchange
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4.7. Counter-current exchanger
Cold Nitrogen
Cold Nitrogen
Hot Nitrogen
-100C
0C
-5C -100C
-95C
-5C -10C
-5C
-10C
Same number of hot passages and cold passages
Temperature of Hot Nitrogen at the end of the exchanger ?
4. Heat Exchange
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4.8. T Warm End definition
Brazed aluminium HX
T cold = 0C
AirWN2
GAN
T cold
T warm
end
T warm end ~ 2C
Loss of cold capacity to beproduced by the turbine
4. Heat Exchange
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4.9. Basis about heat exchange diagram
Temperature (C)
Exchan
gedheat(k
cal/h)
Coldcom
posite
Hotc
ompo
site
-100C
0C
-5C -100C
-95C
N2
N2
Air
-5C -50C
-45C
-50C
0-95 -5-100
T Warm End ?
4. Heat Exchange
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4.10. Real heat balance diagram for APSA L
0
200000
400000
600000
800000
1000000
1200000
1400000
-200 -150 -100 -50 0 50
Temperature (C)
H Heat flow (kcal/h)
Hot composite
Cold composite
4. Heat Exchange
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4.11. Heat balance
T
HT1
T2T3
T4T1
T2T3
T4Warm end
Cold end
QC
QF
Heat Balance :Heat Balance :
H = HC
= QC
. CpC
. ( T2
T1
)
= -
HF = -
QF . CpF . ( T4 T3 )
H = Q . Cp . T
4. Heat Exchange
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4.12. Heat exchange exercise
25C
T=?-100C
20C
Warm end
Cold end
8 Nm3/h
5 Nm3/h
AIR
NITROG
EN
We consider a counter flow
exchanger
We want to warm up 5 Nm3/h ofN2 from - 100 to 20C at 1 bar abs
A 8 Nm3/h flowrate of Air is
available at 25C and 5 bar abs
Cp(Air) = 0.31 kcal/Nm3/C
Cp(N2) = 0.31 kcal/Nm3/C
Air temperature at cold end ?
4. Heat Exchange
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4.13. Heat exchange exercise result
25C
T= -50C-100C
20C
Warm end
Cold end
8 Nm3/h
5 Nm3/h
AIR
NITROG
EN
Heat exchanged by Nitrogen
HN2
= 5x0.31x[20-(-100)] = 186 kcal/h
Heat exchanged by air
HAIR
= 8x0.31x[T-25]
But HN2 = - HAIR = 186 kcal/h Then 8x0.31x[T-25] = -186 kcal/h
Finally T = -186/(8x0.31)+25 = -50C
4. Heat Exchange
4 14 I fl f f l t h t h
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4.14. Influence of f lowrate on heat exchange
Flow evolution T warm end T cold end
Hot fluid
Cold f luid
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4. Heat Exchange
4 16 C t fl t
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4.16. Counter flow arrangement
Parting sheetParting sheet
Parting sheetParting sheet
Spacer barSpacer bar
Exchange finExchange fin
FlowrateFlowrate
Spacer barSpacer bar
Perforated finsPerforated fins
HeringboneHeringbonefinsfins
SerratedSerratedfinsfins
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4. Heat Exchange
4 18 Different type of distributors
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19PERU LNG - 2009
4.18. Different type of distributors
4. Heat Exchange
4 19 Different type of fins
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4.19. Different type of fins
Straight fins
Perforated fins
Serrated fins
Heringbone
fins
4. Heat Exchange
4 20 General view of the heat exchanger
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4.20. General view of the heat exchanger
--
AssemblyAssembly
--
Outlet fluidOutlet fluid
--
CoreCore
--
HeaderHeader
--
NozzleNozzle
--
WidthWidth
--
StackStack
--
LengthLength
--
PassesPasses
--
Side plateSide plate
--
Parting sheetParting sheet
--
Heat transfer finsHeat transfer fins
--
Distributor finsDistributor fins
--
Spacer barSpacer bar
--
End barEnd bar
6611
22
33
44
55
77
88
99
1010
1111
1212
1313
1414
1515
33
55
11
22
44
66
77
88
99
1010
1111
1212
11
331414 1515
4. Heat Exchange
4 21 General view of the heat exchanger
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4.21. General view of the heat exchanger
4. Heat Exchange
4 22 Warm end Embrittlement hazard
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4.22. Warm end Embrittlement hazard
Nitrogen piping at warm end of the Heat Exchanger is not
designed for cryogenic temperature
Occasionally, there can be cold f luid ingress at the warm end :
During process deviation
During stop of the plant
Precautions must be taken to prevent cold embritt lement
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COLD PRODUCTIONCOLD PRODUCTIONCOLD PRODUCTION
6. Cold Production
6.1. Energy balance principle
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6.1. Energy balance principle
Heat inlet
or
Cold losses
Heat losses
or
Cold inlet
APSA-L
)()( outletheatinletheat =
6. Energy Balance & Cold Production
6.2. Cold balance application
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3PERU LNG 2009
6 C pp
GAN LIN
R01 R02
D01Air
inlet
C01 K01
{
8 bar g
40C
0.1 bar g
35C
7 bar g
-171CWarmend T
Liquid
production
Insulation
losses
Turbine
work
6.3. Energy balance
6. Cold Production
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gy
Cold losses or heat inlets
Heat exchanger warm end temperature difference
Liquid production
Heat entrance due to non perfect insulation
Cold inlets or heat losses
Turbine work
Isotherm expansion of products
Liquid assist
6. Cold Production
6.4. Cold balance comparison
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p
Small units Large plants
Insulation
Warm end T
Liquid production
GAS LIQUID GAS LIQUID
70% 7% 20% 1%
30% 2% 80% 3%
0% 91% 0% 96%
6. Cold Production
6.5. Why a Cold Production is required ?
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6PERU LNG 2009
y q
AIM
START-UP: COOL DOWN
To ensure a decrease of the temperature in the cold box
NORMAL RUN: ENERGY BALANCE
To maintain the cold balance of the plant
HOW
By withdrawing some heat out of the cryogenic system
By expansion of air
6. Cold Production
6.6. Turbine principle
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7PERU LNG 2009
Symmetric work to the one of a centrifugal compressorSymmetric work to the one of a centrifugal compressor
Compresseur Turbine
6. Cold Production
6.7. Turbine thermo-dynamical Principle
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Compressor / Pump Turbine
Theorem of Bernoulli : csteE2
VP=+
Static pressure Dynamic pressure
6. Cold Production
6.8. Turbine thermodynamical Principle
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Increase in the gas speed without energywithout energy
extractionextraction in the inlet vanes (1)
static pressure diminishesstatic pressure diminishes
Decrease in the gas speed with energywith energy
extractionextraction in the relaxation wheel (2)
dynamic pressure diminishesdynamic pressure diminishes
Decrease in the gas speed without energywithout energyextractionextraction in the diffuser (3)
dynamic pressure is transformed into staticdynamic pressure is transformed into static
pressurepressure
1
2 3
6. Cold Production
6.9. Turbine overview Entrance gas process
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Outinggasprocess
Turbine
body
6. Cold Production
6.10. Turbine wheels
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11PERU LNG 2009
Gas
entrance
Gas outing
6. Cold Production
6.11. Turbine wheels
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Adjustable diffuser(IGV)
Wheel of the turbine
Arrival of thefluid by the
volute
Discharge
6. Cold Production
6.11. Speed tr iangle
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13PERU LNG 2009
0
1
2
0
1
2
Fixed part : Distributor
Mobile guide
vanes
Wheel
3
1U
r
1Vr
1Wr
2Ur
2Vr
2W
r
6. Cold Production
6.12. How braking cryogenic turbines ?
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14PERU LNG 2009
BrakingBraking of the turbine
Energetic stability
ConsumptionConsumption of this energy
Oil spin-dry
pump
Electrical
generator
Air
brake
Booster
brake
Oil
brake
Production of mechanical energyProduction of mechanical energy with the expansion wheel
6. Cold Production
6.13. APSA-L Oil brake turbine principle
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15PERU LNG 2009
- Figure of an oil brake -
Turbine wheel
Oiled contact surface
6. Cold Production
6.14. APSA-L cold production equipment
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Air
Oil Tank
Water
Air
6. Cold Production
6.15. APSA-L PERU LNG : LIN Production Case
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17PERU LNG 2009
LRV
Turbine -19kW
19kW
S = 43000 rpm
F = 1650 Nm3/h
P = 0.2 bar g
T = -184C
F = 1650 Nm3/h
P = 4.3 bar g
T = -148C
6. Cold Production
6.16. Cryostar ECO turbine
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18PERU LNG 2009
Oil tank
Oil brake valve
6. Cold Production
6.17. Cryostar ECO turbine
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19PERU LNG 2009
Oil cooler
Oil pump
Oil tank
6. Cold Production
6.18. Turbine elements
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20PERU LNG 2009
Expander stage Oil brake sleeve in bearing housing
6. Cold Production
6.19. Expansion turbine behaviour
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21PERU LNG 2009
2 choices to increase the cold production of the plant:
increase the turbine inlet pressure of 100 mbar
decrease the turbine outlet pressure of 100 mbar
What is the best choice ?EXPANSION POWER VARIATION VS P VARIATION EITHER ON MP SIDE OR BP SIDE
15
15.1
15.2
15.3
15.4
15.5
15.6
15.7
15.8
15.9
16
16.1
0 10 20 30 40 50 60 70 80 90 100
DP (mbar)
Power(kW)
POWER BP VAR (KW)
POWER MP VAR (kW)
GAIN MP
GAIN BP
ConclusionBe careful withthe pressure on
the BP side of
the turbine.
Quick loss of cold
production
6. Cold Production
6.20. P&ID : Expansion turbine
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22PERU LNG 2009
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1PERU LNG -2009
AIR DISTILLATION
PRINCIPLE
AIR DISTILLATIONAIR DISTILLATION
PRINCIPLEPRINCIPLE
Distillation
Goal and principle
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2PERU LNG -2009
GOAL
To separate Nitrogen and Oxygen from atmospheric Air
PRINCIPLE
Separation by Distillation : Content difference between
liquid and vapour phases
KEY PARAMETERS
Boiling Point
Liquid vapour equilibrium
Fractional distillation
Reflux
WATER + ALCOHOL MIXTURE:
ALCOHOL t l til t
PRINCIPLEPRINCIPLEPRINCIPLEDistillation
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LIQUID:
enriched in leastvolatil
component::
WATER
VAPOUR:
enriched in most
volatilcomponent::
ALCOHOL
BOILING
ALCOHOL: most volatil component
WATER: least volatil component
LIQUID Mixture
Two components:
WATER +ALCOHOL
APSA03/Distill1/VA#1
AIR = MIXTURE NITROGEN (79 %) + OXYGEN (21 %)
t l til t NITROGEN
PRINCIPLEPRINCIPLEPRINCIPLEDistillation
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4PERU LNG -2009APSA03/Distill1/VA#2
most volatil component : NITROGENleast volatil component : OXYGEN
LIQUID:enriched in least
volatil
component::
OXYGEN
VAPOUR:
enriched in mostvolatil
component::
NITROGEN
BOILING
LIQUID AIR
-200C, 1 b abs
At the boilling point, there are two phases:
At the boilling point, there are two phases:
Boiling Point dfinitionBoilingBoiling Point dPoint dfinitionfinitionDistillation
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5PERU LNG -2009
VAPOUR
LIQUID
P, T
- a boil ing LIQUID
- a release of VAPOUR
- a boil ing LIQUID
- a release of VAPOUR
Thus we define a
LIQUID-VAPOUR EQUILIBRIUM
Thus we define a
LIQUID-VAPOUR EQUILIBRIUM
A boiling point is defined with:
- a TEMPERATURE T
- a PRESSURE P
A boiling point is defined with:
- a TEMPERATURE T
- a PRESSURE P
Boiling point values and volatility scale
Boiling PointsBoilingBoiling PointsPointsDistillation
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6PERU LNG -2009
Boiling point values and volatility scale
Name SymbolMolecular
Weight (g)
Boiling Temperature @
1,013 bar abs.
Helium He 2 -269 C
Hydrogen H2 2 -253C
Neon Ne 20 -246C
Nitrogen N2 28 -196C
Air Air 29 -191C
Argon Ar 40 -186C
Oxygen O2 32 -183C
Kripton Kr 84 -153C
Xenon Xe 131 -108C
At the boiling point, if one parameter changes (Pressure or Temperature), the other
parameter has to change too:
Boiling PointsBoilingBoiling PointsPointsDistillation
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7PERU LNG -2009
VAPOUR
LIQUID
11 b abs
- 168 C
VAPOUR
LIQUID
1 b abs- 196 C
VAPOUR
LIQUID
3.6 b abs
- 183 C
VAPOUR
LIQUID
1 b abs- 183 C
VAPOUR
LIQUID
3.6 b abs
- 168 C
VAPOUR
LIQUID
11 b abs
- 152 C
NITROGEN OXYGEN
If the Pressure increases the Temperature has to increase too
PRESSURE AND TEMPERATURE RELATIONSHIP:
Boiling Points CurvesBoilingBoiling PointsPoints CurvesCurvesDistillation
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8PERU LNG -2009
If the Pressure increases, the Temperature has to increase tooOR
If the Temperature increases, the Pressure has to increase too
AND inversely.
Do les courbes des points dbullition:4
Pressure = f (Temperature) Temperature = f (Pressure)
Curves: Liquid state and Gaseous state separation
P
T
T
P
LiquidState
Gaseous
State
LiquidState
Consequence: the boiling point curves
APSA03/Distill1/VA#6
GaseousState
Nitrogen versus Oxygen
Distillation Boiling PointsBoilingBoiling PointsPoints
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9PERU LNG -2009
ISOBARICISOBARICISOBARIC
NITROGENNITROGEN OXYGENOXYGEN
- 196 C
- 183 C
1 b abs
VAPOUR
LIQUID
VAPOUR
LIQUID
4.5 b abs 1.3 b abs
OXYGENOXYGENOXYGENNITROGENNITROGENNITROGEN
ISOTHERMALISOTHERMALISOTHERMAL
- 180 C
Nitrogen is more volatil than Oxygen:
-NITROGEN = most volatile component
-OXYGEN = least volatile component
Nitrogen is more volatil than Oxygen:
-NITROGEN = most volatile component
-OXYGEN = least volatile component
For an OXYGEN-NITROGEN MIXTURE at the LIQUID-VAPOUR
EQUILIBRIUM
For an OXYGEN-NITROGEN MIXTURE at the LIQUID-VAPOUR
EQUILIBRIUM
Distillation Nitrogen - Oxygen mixtureNitrogenNitrogen -- Oxygen mixtureOxygen mixture
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10PERU LNG -2009
EQUILIBRIUM,
NITROGEN being the most volatile component:
EQUILIBRIUM,
NITROGEN being the most volatile component:
OO22++NN22
OO22++NN22
P, T
(the Vapour phase and the Liquid phase are called CONCOMITANT PHASES)(the Vapour phase and the Liquid phase are called CONCOMITANT PHASES)
- the liquid phase BECOMES LESS
CONCENTRATED IN NITROGEN:
CONSEQUENTLY, IT BECOMESENRICHED IN OXYGEN
- the liquid phase BECOMES LESS
CONCENTRATED IN NITROGEN:
CONSEQUENTLY, IT BECOMES
ENRICHED IN OXYGEN
- the vapour phase BECOMES ENRICHEDIN NITROGEN
- the vapour phase BECOMES ENRICHEDIN NITROGEN
VAPOUReven more
Distillation Fractional DistillationFractional DistillationFractional Distillation
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11PERU LNG -2009
VAPOUReven more
enriched in
NITROGENNITROGEN
CONDENSER
1st BOILING
2d BOILING
VAPOUR:
enriched in
NITROGENNITROGEN
LIQUID:
enriched in
OXYGEN
Liquefaction:Liquid enriched in
NITROGENNITROGEN
VAPOUR:
"PURE" NITROGEN
N
Distillation Fractional DistillationFractional DistillationFractional Distillation
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12PERU LNG -2009
LIQUID:
"PURE" OXYGEN
VAPOUR
MORE
ANDM
OREENRIC
HEDI
NNITR
OGEN
LIQUID
MOREAN
DMOR
EENR
ICHED
INOX
YGEN
(liquid
flowsdown
bygravi
ty)
Successive Boilings and
Liquefactions
APSA03/Distill1/VA#10
ISOBARIC SYSTEM:
pressure is the same in each vessel
ISOBARIC SYSTEM:
pressure is the same in each vessel
-- 196196 CC"PURE" NITROGEN
Distillation Fractional DistillationFractional DistillationFractional Distillation
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13PERU LNG -2009
-- 183183 CC"PURE" OXYGEN
pressure is the same in each vessele.g.: 1 b abs
pressure is the same in each vessele.g.: 1 b abs
CONSEQUENCE:
TEMPERATURE
GRADIENT
CONSEQUENCE:
TEMPERATURE
GRADIENT
-- 196196 CCPURE NITROGEN
APSA03/Distill1/VA#11
SUPPRESSION OF THE BOILERS AND CONDENSERS
For that, we achieve a LIQUID-VAPOUR CONTACT:
Vapour:
HOTTER
Distillation LIQUID VAPOUR CONTACTLIQUIDLIQUID VAPOUR CONTACTVAPOUR CONTACT
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14PERU LNG -2009
LIQUID
(colder)
VAPOUR
(hotter)
Boil ing of the LIQUID =
VAPOUR
Liquefaction of
the VAPOUR =
LIQUID
LIQUID VAPOUR CONTACT
Heat Transfer
(calories)
,the Vapour passes through the Liquid in the vessel
- the vapour HOTTER, makes the liquid boiling
- the liquid COLDER, condenses the vapour
APSA03/Distill1/VA#12
Liquid:
COLDER
LIQUID-VAPOUR
Contact
SUPPRESSION OF THE BOILERS AND CONDENSERS
Distillation LIQUID VAPOUR CONTACTLIQUIDLIQUID VAPOUR CONTACTVAPOUR CONTACT
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TEMP
ERATU
REGR
ADIEN
T:
Vapouri
shott
er
Liquid
iscolde
r
We only need:
One boiler at the bottom
One condenser at the top
We only need:
One boiler at the bottomOne condenser at the top
BOILER
CONDENSER
CONDENSER
MOST VOLATILE
Distillation Fractional Distillation : ColumnsFractional Distillation : ColumnsFractional Distillation : Columns
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16PERU LNG -2009
BOILER:
Vaporizer
VAP
OUR
BECOMESR
ICHER
IN
MOSTV
OLATILE
COM
PONENT
L
IQUID
BECOMESR
ICHER
IN
LEAST
OLATILE
CO
MPONENT
LIQUID-VAP
OUR
CONTAC
T
LIQUID-VAP
OUR
CONTAC
T
DISTILLATION
COLUMNS:
DISTILLATION
COLUMNS:
TRAYSTRAYS
PACKINGPACKING
COMPONENT
LEAST VOLATILECOMPONENT
LABORATORY
Device
LABORATORY
Device
CONDENSER
Distillation Regular ColumnRegular ColumnRegular Column
GAN
Condenser
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17PERU LNG -2009
VAPORIZER
GOX DRAW-OFF
LOX DRAW-OFF
LIN DRAW-OFFGAN DRAW-OFF
AIR FEED
VAPOUR
LIQ
UID
=REFLUX
PACKING
SECTIONS
AIR
LIN
GOX
Vaporizer
LOX
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FOR A GAS NITROGEN PRODUCTION, ONLY THE UPPER
SECTION OF THE COLUMN IS NECESSARY:we do not need the lower section
From the regular column to the APSAFromFrom thethe regularregular columncolumn to the APSAto the APSADistillation
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19PERU LNG -2009
CONDENSER
VAPORIZER
GOX DRAW-OFF
LOX DRAW-OFF
LIN DRAW-OFFGAN DRAW-OFF
AIR FEED
VAPOUR
LIQ
UID
we do not need the lower section
CONDENSER
AIR FEED
LIN DRAW-OFFGAN DRAW-OFF
From the regular column to the APSAFromFrom thethe regularregular columncolumn to the APSAto the APSADistillation
EQUIPMENTS NEEDED
CONDENSER
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20PERU LNG -2009
EQUIPMENTS NEEDED:
- PACKING SECTION
- CONDENSER AT THE TOP
- AIR FEED IN GASEOUS STATE
- GAN DRAW-OFF
- LIQUID WASTE OUTLET
AIR FEED
GAN DRAW-OFF
PACKING
SECTION
Air feed must be in gaseous state,in order to build-up the
up-coming vapour:so that the vaporizer is
no longer necessary
LIQUID WASTE
OUTLET
INCOMING MATERIAL QUANTITY= OUTGOING MATERIAL QUANTITY
INCOMING MATERIAL QUANTITY= OUTGOING MATERIAL QUANTITY
Distillation Material BalanceMaterial BalanceMaterial Balance
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21PERU LNG -2009
400 Nm3/h THE LIQUID WASTE IS THE
CONSEQUENCE OF THE MATERIAL
BALANCE:
Flowrate, O2 content
ITS O2 CONTENT IS ALWAYS HIGHER
THAN THE ONE OF AIR;
For that, this liquid is called:
RICH LIQUID
THE LIQUID WASTE IS THE
CONSEQUENCE OF THE MATERIAL
BALANCE:Flowrate, O2 content
ITS O2 CONTENT IS ALWAYS HIGHER
THAN THE ONE OF AIR;For that, this liquid is called:
RICH LIQUID
Flowrate = 1000 - 400 = 600 Nm3/h
O2 = = 35 %600
1000 x 21 %
1000 Nm3/h
O2 = 21 %
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DEFINITION: Heat quantity necessary to vaporize totally
1 kg of liquid
DEFINITION: Heat quantity necessary to vaporize totally
1 kg of liquid
Distillation LATENT HEAT OF VAPORIZATIONLATENT HEAT OF VAPORIZATIONLATENT HEAT OF VAPORIZATION
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23PERU LNG -2009
1 kg
Liquid
1 kg
Vapour
Heat quantity: kcal
OXYGEN: 51 kcal (-183 C, 1 b abs)
NITROGEN: 47.6 kcal (-196 C, 1 b abs)
OXYGEN: 51 kcal (-183 C, 1 b abs)
NITROGEN: 47.6 kcal (-196 C, 1 b abs)
APSA03/Distill2/VA#5
OBJECTIVES:
To liquefy gas nitrogen at the topof the column in order to achieve
CONDENSER
Distillation Vaporizer - Condenser systemVaporizerVaporizer -- Condenser systemCondenser system
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24PERU LNG -2009
PRINCIPLE:
We need a specific device to draw-off the connecting heatquantity from gas nitrogen.
GAN LIN
Heat quantity
DRAWN-OFF
of the column in order to achieve
the Reflux.LINGAN
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Vaporized
RICH LIQUID
VaporizedRL RLHeat
TRANSFER
Upper part
Distillation Vaporizer - Condenser systemVaporizerVaporizer -- Condenser systemCondenser system
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26PERU LNG -2009
LIN
GAN
EXCHANGER
GAN LINTRANSFER
APSA column
RICH LIQUID
bath
AN EXCHANGER IS LOCATED AT THE TOP OF THE COLUMN
IN ORDER TO ACHIEVE THE HEAT TRANSFER BETWEEN
RICH LIQUID AND GAN
VAPORIZER CONDENSER
VAPORIZED RICH LIQUIDRICH LIQUID
VALVE
Distillation APSA column : final constructionAPSA column : final constructionAPSA column : final construction
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VAPORIZER - CONDENSER
GAN DRAW-OFF
GASEOUS AIR
RICH LIQUID BATH
BOTTOM RICH LIQUID
E02
K01
RICH LIQUIDPIPE
Distillation Reflux Ratio R : definit ionReflux Ratio R : definitionReflux Ratio R : definit ion
L
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AIR
GAN
RL
V
L
Where:
V = Vapor Flowrate (Nm3/h)
L = Liquid Flowrate (Nm3/h)
R =L
V
R = LV
Distillation Reflux Ratio R : definit ionReflux Ratio R : definitionReflux Ratio R : definit ion
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V L
AIR
GAN
LR
GAN
AIR
V
Where:
L = V GANand
V = Air
Consequently, R = f (GAN & Air flow rates) :
R =Air GAN
Air
Incomming
N2 amount
Outgoing
N2 amountL/V
Air GAN RL Total
Distillation Reflux Ratio R variationReflux Ratio R variationReflux Ratio R variation
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1000x79% =
790
400x100% =
400
600x65% =
390 790390/790=
0.49
1000x79% =
790450x100% =
450390 840
340/790=
0.43
The column becomes less concentrated inNitrogen :
Consequently, the column becomes enriched in
Oxygen
The GAN purity decreases (O2 content
increase)
The GAN purity decreases (O2 content
increase)
AIR
GAN
LR
Distillation Conclusion : Reflux Ratio impactConclusion : Reflux Ratio impactConclusion : Reflux Ratio impact
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AIR
GAN
RL
V
L GAN
R = L/V
% N2 GAN(GAN Purity)
TECHNOLOGY : Packing elementTECHNOLOGY : Packing elementTECHNOLOGY : Packing elementDistillation
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AST (Advanced Sieve Trays)
Benefits :
Very efficient liquid vapour contact
Low pressure drop (liquid film distribution)
High operating flexibility (minimal / maximal gas load)
High capacity (maximal gas load)
Low inertia
Distillation TECHNOLOGY : Packing elementTECHNOLOGY : Packing elementTECHNOLOGY : Packing element
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Structure: assembly of corrugated metallic sheets (aluminium).
The Liquid-Vapour contact is obtained bythe division of the liquid on the
corrugated-crossed sheets: the liquid f ilm
Distillation TECHNOLOGY : Packing elementTECHNOLOGY : Packing elementTECHNOLOGY : Packing element
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Corrugated-
crossed aluminium
sheets
Perforations
corrugated crossed sheets: the liquid f ilm
is drawn downwards by gravity while the
gas (vapour) flows upwards through the
perforations and the void spaces between
the sheets.
Distillation VaporizerVaporizerVaporizer
GOAL
to condense gas at the top of the disti llation column in
Vaporizer - Condenser
VaporizerVaporizer -- CondenserCondenser
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PRINCIPLES
Heat exchange in an aluminium brazed Heat ExchangerCounter flow arrangement
Heat flux from the Hot fluid to cold fluid
Driving force = temperature difference
AIR
GAN
LR
to condense gas at the top of the disti llation column in
order to ensure a liquid reflux in the column
to vaporise Rich liquid fluid at a lower pressure in order to
feed the turbine (APSA L/LE) or the booster (APSA LE)
E02 Vaporizer
VaporizedRICH LIQUID
TECHNOLOGY : Bath type vaporiser
KEY COMPONENT FOR THE PRESSUREMAP AND FOR THE COLD PRODUCTION
Distillation VaporizerVaporizerVaporizer
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-172C
4.8b
-170C
9.7b
Incondensable
gases
APSA column
RICHLIQUID
bath
SAFETY : in all cases the vaporiser must
be completely submerged
LIN
GAN
EXCHANGER
T= 2C
RL
RL + VRL
GAN
GAN
LIN
LIN
AIR downstream the Air Purification still Contents some contaminants:
Distillation Vaporizer deconcentration purgeVaporizerVaporizer deconcentrationdeconcentration purgepurge
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HYDROCARBONS
N2O
A PART OF THESE COMPONENTS ARE STOPPED IN THE
PURIFICATION UNIT
THE OTHER PART ENTER IN THE COLD BOX
The light components go up (ex: H2
,)
The heavy component go within the vaporiser bath (RL)
AMONG THESE HEAVY COMPONENTS, SOME ARE NOT VAPORISED
Distillation Vaporizer deconcentration purgeVaporizerVaporizer deconcentrationdeconcentration purgepurge
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CONCLUSION : WITHOUT ANY PURGE IT COULD HAPPEN AN
ACCUMULATION OF HYDROCARBONS WHICH CAN FORM
EXPLOSIVE COMPLEXES WITH RICH LIQUID BATH
TO AVOID ACCUMULATION, THE BATH MUST BE PURGED
PERMANENTLY
DECONCENTRATION PURGE :
DIRECTLY LINKED TO THE SAFETY OF THE PLANT
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MASS BALANCEMASS BALANCEMASS BALANCE
)()( outletinlet =
7. Mass balance
7.1. Mass balance formula
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)()( outletinlet
GLOBAL MASS BALANCE
inlet flowrate = outlet flowratePARTIAL MASS BALANCE
inlet flowrate,i = outlet flowrate,i inlet N2 flowrate = outlet N2 flowrate
APSA LAPSA L
GANGAN
Residual GasResidual Gas
AIRAIR
7. Mass balance
7.2. Mass balance application
Residual GasResidual GasGLOBAL MASS BALANCE
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APSA LAPSA L
GANGAN
Residual GasResidual Gas
AIRAIR
QAir = QRes + QGAN
whereQAir = inlet air flowrate
xAir = inlet air Nitrogen composition
PARTIAL MASS BALANCE
QN2,Air = QN2,Res + QN2,GAN
xAir.QAir = xRes.QRes + xGAN.QGAN
7. Mass balance
7.3. Mass balance exercise
Residual GasResidual Gas
A customer want to produce N2 ata purity of 1ppm O2.
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APSA LAPSA L
GANGAN
Residual GasResidual Gas
AIRAIR
He wants to use his air network
producing 4000 Nm3/h.
A classical O2 content in the
Residual gas is 30 % for such a
plant.
Argon is not considered in the
calculation
Air composition :78.11 % N2, 0.93% Ar, 20.96% O2
How much Nitrogen he will produce in these conditions ?
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OVERVIEW OF APSA L
CONTROL
OVERVIEW OF APSA LOVERVIEW OF APSA L
CONTROLCONTROL
9. Process Flow Diagram : Warm Skid
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9. Process Flow Diagram : Cold Box
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9. Process Flow Diagram : LIN Storage
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GENERAL SAFETYGENERAL SAFETYGENERAL SAFETY
Safety issues on APSA-L
General Safety Issues
General hazards in industrial environment
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Hazards specific to ASU
CnHm related hazards
Identification
Prevention
General Safety Rules
What kind of risks ?
Running machines
Electricity
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Pressure
Noise
Under-oxygenation (Anoxia)
Over-oxygenation
Cryogenic temperaturesHigh temperatures
Burning
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Example: Pressure hazard (continued)
PIPING AND
CONTAINERS COMPLIANT
WITH CURRENT REGULATIONS
ALWAYS MAKE SURE
THERE IS ZERO PRESSURE
BEFORE SERVICE OPERATIONS
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SAFETY DEVICES
OBSERVE SERVICE OPERATION
PROCEDURES
REPORT ANY DEFECT
OBSERVED ON A DEVICE,
A PIPE
OR SAFETY PART
IMMEDIATELY
SAFETY
MEASURES
-> Design codes
-> Scheduled inspections
-> Tests
32
General Safety Rules
Usual Hazardous works :
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Work at high levels
Digging work
Hoisting and handling equipments
Traffic
Electricity
Machines
Work on piping or vessel
WeldingSources of radioactivity
General Safety Rules
Safety Management
Defining clearly responsibilities
Approvals and qualifications
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Qualified and trained workers
Qualified subcontractors
Procedures
Work permit
Electrical / Mechanical isolation
Equipments
PPE
Certified tools / machinery
EIS Management?
General Safety Rules
Usual Personal Safety equipment
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Helmet
Safety glasses and adequate face shields for specific
hazards (chipping, acid work, welding, molten metals )
Ear plugs and noise-proof head sets
Safety shoesClean and Fire-proof clothing
Safety mittens or gloves
Protective masks with suitable filterSafety belt or harness if necessary
ASU Related Safety
Gas Hazards
Processed gases of ASU involve 2 main specific hazards
1) Inflammation or explosion
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Inflammation or explosion
Causes
Presence of flammable gas in air
Oxygen enriched atmosphere (more than 21% oxygen)
Concerned zones
liquid oxygen filling station oxygen expansion valve station
oxygen metering station
liquid or gaseous oxygen vent
) p
2) Anoxia
O2 gas hazardPROPERTIES .GAS ENABLES AND MAINTAINS COMBUSTION.
SAFETY MEASURES
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WITH AIR
After
analysis
if O = 21%2
DETECTION
No
leaks
O %O %22
O %O %22
IDENTIFICATION
of pipes andstorage locations.
NAMECOLOUR
Purge venting
to the outside
O2 gas hazard (continued)OXYGEN O 22
PERCEPTION
DENSITY/AIR
Colourless, odourless, tasteless.
d = 1.1AIR SPECIAL
PRECAUTIONS
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EFFECT OF OXYGEN ENRICHMENT
ON COMBUSTION
Fuels ignite more easily.
Flames much hotterand spread more quickly
NORMAL PROPORTION IN AIR 21%
PRECAUTIONS
Detection with alarm if %
O in air exceeds 25%.
No grease, no oil.
No particles.
Clean clothing made from
fire resistant textiles-
Controlled speed
with slow manoeuvres.
Floors clean and made from
non combustible materials.
% O in air2
Effect on combustion
25%25%
30%30%
50%50%
FASTER COMBUSTION
QUICK COMBUSTION
INSTANTANEOUS COMBUSTIONEXPLOSIONEXPLOSION
2
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N2 gas hazard
PROPERTIES
18% O
21% ONormal breathing
Vertigo,
headaches
Asphyxia
GAS DOES NOT SUPPORT LIFE.
WHEN THESE GASES ARE PRESENT:THE QUANTITY OF O DECREASES,
ATMOSPHERE UNDER OXYGENATED,2
2
2
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WITH AIR
SAFETY MEASURES0% O
,
ASPHYXIA.
2
orAfter
analysisif O = 21%2
If O < 18%2
DETECTION
Alarm
if O
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Effects
Every touch with liquefied gas causes frostbite similar to burnSkin and lungs can be damaged by cold atmosphere
Lower the temperature, longer the touch, more serious effects are
Hypothermia can cause death Safety rules
Do not touch cold material
Do not stay in a cold atmosphere
Do not walk in a zone where cryogenic liquid has flown
Do not purge voluntarily cryogenic liquids on the ground
Take care of wet clothes
ASU Related Safety
Operating in Heat Insulated Area
Perlite Insulation (cold box, exchanger box)Perlite : hydrated silicate pre-submitted to an expansion
Highly irritant material to be handled with gloves, glasses
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Highly irritant material to be handled with gloves, glasses
and maskExtremely light and fluid (a fall in perlite lead to death)
Rock-wool insulation (cold tank, exchanger box)
Highly itching material
Work in a tunnel highly dangerous (risk of collapsing)
Nearly all heat insulated area are considered CONFINED
SPACE specific entry rules apply
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HYDROCARBONS SAFETYHYDROCARBONS SAFETYHYDROCARBONS SAFETY
Hydrocarbons Safety
1. CnHm Hazards: Explanations1. Risks related to the impurities in the bath type vaporizers
2. Right/wrong operation of the E02 vaporizer
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g g p p
3. Right/wrong operation of the front end purification (FEP)
2. Hazards Controls:The 8 Golden Rules
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Hydrocarbons Safety
Bath type vaporizer operation (APSA-L)
InternalInternal type (main vaporiser E02)type (main vaporiser E02)
LP
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Important RECIRCULATION of l iquid(thermosiphon effect):
- around 1 Nm3 vaporised *
- for 50 Nm3 of non-vaporised LR *
* figures corresponding to an exchanger
completely immersed
Rare gases purge
Ne, He, H2
LP
HP
LR Purge
GAN & LIN Prod.
LRV
Hydrocarbons Safety
Proper and Wrong operation of a bath type vaporizer
Liq = 25 Nm3/h
N2O = 160 ppm
Gas = 100 Nm3/h
N20 =100 ppb
Reduced feedNormal operation
Gas = 100 Nm3/h
+
Liq = 5000 Nm3/h
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Heat to vaporise 100
Liq = 5100 Nm3/h
N20 = 40 ppm
q
N20 = 41 ppm
Liq = 125 Nm3/h
N20 = 40 ppm *
* considering CO2 in that case, only 1 ppm in
the feed would lead to deposit
Heat to vaporise 100
DEPOSIT N2O
Hydrocarbons Safety
Proper and Wrong operation of a bath type vaporizer
CORRECT VAPORISATION DRY VAPORISATION
GAS LIFT
STOPPED
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Gas lif t in
normal
operation.Recycling
= up to
50 times
the vaporised
flowrate
Solubility limit is
reached. Deposits of
CnHm, CO2 or N2O
are
building up
Concentration is
increasing
TOO LOWLEVEL
Hydrocarbons Safety
Proper and Wrong operation of a bath type vaporizer
DISTILLATION after plugingof a channel in the vaporiser
Pluging by solid :
- suspended sol ids
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p
(aerosol of oi l - dust of
adsorbent)
- dissolved impurities
CO2, N2O after
reaching the solubility
limit.
Then concentration
in liquid impur ities
(CH4 - C3H8 - C2H6)
Hydrocarbons Safety
Proper and Wrong operation of a bath type vaporizer
Normal Operation:
Excess liquid flowing out
No concentration
Dry Boiling:
No liquid out
Concentration build up
Deposit starts if liquid
gets saturated and
Contaminants cannot be
eliminated wi th the gasNormal level
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phaseNormal level
Low level Low level
Hydrocarbons Safety Application: APSA-L E02 Vaporizer
LRV
CnHm enter CnHm exit
VAPO
E02ININ Q
LRVLRV Q
LRLR Q
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LR
LR
AIRAIR
LRLRV
AIRAIRLR
Q
Q
QQK
Q =
+
Q
Purge Rate = 0.2% of AIR FLOW
Concentration factor = 500Air content LOX content
CH4 = 5 ppm CH4 = 2500 ppm
C2H6 = 0.2 ppm C2H6 = 100 ppm
C2H2 = 0.5 ppm C2H2 = 250 ppm
Purge Rate = 0.2% of AIR FLOW
Concentration factor = 500Air content LOX contentCH4 = 5 ppm CH4 = 2500 ppm
C2H6 = 0.2 ppm C2H6 = 100 ppm
C2H2 = 0.5 ppm C2H2 = 250 ppm
PI4.2 barg
Hydrocarbons SafetyAdsorption Principles
The Front End Purif ication (FEP)is designed to stop completely :
H2O
CO2
H2O and CO2free air
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CO2
But other impurities
from the air pass through
the adsorber before CO2 :
CH4 Methane
C2H6 Ethane
C3H8 Propane
N2O Nitrous Oxide
C2H4 Ethylene
Air with all
contaminantsREACTIVATION
ADSORPTIO
N
And may enter into the Cold BoxAnd may enter into the Cold Box
Hydrocarbons SafetyAdsorption capacity of Front End Purification
aton
aton
totalH2O, CO2,
nC4H10, C2H2, O3.
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Frontend
Frontendpurific
a
purifica
partial
none
N2O, NO2,
C2H4
ADSORPTIONADSORPTIONLEVELSLEVELS
C3H8,
NO
H2, CO,H2, CO,
CH4, C2H6CH4, C2H6
Hydrocarbons Safety Contaminants dangerous for the purif ication
Some CONTAMINANTS can badly damageSome CONTAMINANTS can badly damage
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They are mainly:They are mainly:
-- the acid gases : CI2, SO2, H2S etc., NH3the acid gases : CI2, SO2, H2S etc., NH3
-- miscellaneous organic moleculesmiscellaneous organic molecules
the molecular sievesthe molecular sieves
Hydrocarbons Safety Potential hazards in the Front End Purification
Abrasion of a part of the adsorbent (velocity too high)
Risk of channeling = by pass flow
Risk of lower adsorption capacity
Risk of introducing adsorbent dust in the cold box
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Internal bypass of the beds, by leakage Liquid water carry-over (separation problem) :
CO2 adsorption capacity is reduced if water vapor reaches the molecular
sieve
A part of the adsorbent can be destroyed Presence of some aerosols which go through the FEP
Presence of dangerous contaminants in the mole sieve
Too long adsorption phase :
break-trough of CO2 or H2O
Example of CO2 entering an APSA L4 :
-10 ppb of CO2 entering continuously : 2 kg per year
-2 ppm of CO2 during 15 minutes : 15 grams of deposit
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Hydrocarbons Safety Event sequence to explosion
Spontaneous ignition of reactive
material on Aluminum platefin
main vaporizer in cold box
Explosive rupture of
cryogenic distillation
column
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Presence of airborne fuel
- aerosols light hydrocarbons -
concentration/accumulation in
LOX & on Aluminum surfaces -
with N2O or CO2 ice & dry-boiling
Combust ion of accumulated
hydrocarbon contaminants
on Aluminum vaporizer cores
Massive runaway combustion
of Aluminum exchangers inoxygen (exothermic reaction)
Flash vaporization
of cryogenic liquid
Uncontrolled escalation
to explosion
Hydrocarbons Safety Risks related to the impurities in the vaporizers
During the operation of the ASU, the concentration of impurities in the bath ofthe vaporiser may lead to strong explosions :
- Hydrocarbons, such as Ethane, Propane, Ethylene, Acetylene, or aerosols, can
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concentrate and/or deposit. The Lower Inflamability Limit is reached in LOX- Ozone is a strong ignition agent
These explosion hazards exist when there is a lack of LOX (LR) feed into the
passages, caused by :- Too low level of the bath of the vaporiser
- Plugging of passages by solid deposits: CO2* , N2O*, dust...
* Risk of accidental deposit of CO2 or N2O, due to their low solubility in LOX,5 ppm and 160 ppm respectively.
Hydrocarbons Safety Possible Damage Overview
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Hydrocarbons Safety How to control the CnHm hazards
The 8 GOLDEN RULES1. Environmental Survey
2. Operation of FEP
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3. Operation of Vaporizer4. Deconcentration purge
5. Periodical Deriming
6. Control of the transient phases
7. Control of other sources of pollution
8. EIS management
Hydrocarbons Safety
1. Environmental Survey
1. Surrounding industries and distances
2. Atmospheric conditions
3. Air analysis
4. Communication with surrounding industries
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g
The plant operator shall maintain an environment
file including following information :
Nearby industries liable to release gases
Distances between those potentials sources and theair intake of the ASU (+ height of sources)
Presence of haze (organic aerosols)
Polluted site or Not ?
Hydrocarbons Safety
2. Operation of FEP
Complete retention of CO22 in FEP is of vital importance forthe unit (low solubility in RL : 5 ppm at 181C)
Air conditions evolutions have an impact on :
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Mass Flow RatePressure
Temperature
Duration of the adsorption
Air Cleanliness
Regeneration conditions act on :
Regeneration gas flow rate
Duration of heating
Heating temperature
Hydrocarbons Safety
2. Operation of FEP
FEP performance control : CO22 content analysis at outlet1 ppm Alarm
3 ppm Shutdown of the unit after 15 minutes
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Control of the desorption effectiveness : temperature peak
Alarm in case of no heat peak
Recommended REGEX operation after CO2 breakthrough
test (3 years)
Hydrocarbons Safety
3. Control of the level of bath vaporizer
Upper level tap (100%of the transmitter scale)
Level sample
100% immersion (Level Set Point)LT2
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Lower level tap for LT1
90% immersion (Low Level Threshold)80% immersion (Very Low Level Threshold)
0% immersion
(0% of LT1)
LT170% Lower tap of LT2
Calibration using the heights and the density of the liquid
Check with level sample gaugeTransmitters:
22ndnd
transmittertransmitter= improvement= improvement
Height,m
Plant Shutdown after 1 hour
Hydrocarbons Safety 4. Deconcentration Purge
Deconcentration line: 1/2.LR.04
Deconcentration type: intermittent purge (but permanently
in service)
Deconcentration volume: at least 0.2% of the air flow
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Deconcentration control: sequence linked to the level of
vaporizer E02
Time of purge is constant
Level drop is monitoredAlarm is raised in case of low level drop
Hydrocarbons Safety 5. Periodical Deriming
The objective is to vaporize any contaminants which may
have entered in the equipment of the cold box
Every 3 years
Applied to cold box equipment only (compressor and FEP
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are running independently)Deriming operation
Low pressure
High flow
Deriming mean
Dry air
Usually ambient temperature
Exceptionally hot temperature (65C is the limit for thealuminum heat exchanger)
Refer to PFD
Hydrocarbons Safety 6. Transient Phases
Start-up
As much liquid production as possible
Minimum air input
Liquid assist after first liquid production (LIN only)
S
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Shut-down
Drain ALL liquid after 48h shut-down
Drain if E02 level is below 80% immersion
Change of run-typeMaintain vaporizers level
Normal run
Control of frosted pipes and dead-ends
Hydrocarbons Safety 7. Other sources of pollution
Machine: Turbine
Lubricated machine
Seal gas pressure
Instrument air
U ll d i
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Usually: dry air
Back-up ?
Air intake
Car parking, Truck unloading
Hot works, fires...
Exchanger water leak...
Hydrocarbons Safety 8. E.I.S Management
E.I.S = Element Important for Safety
Safety Protection Loops
Alarm and Shutdowns parameters
Set-points
D l
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Delay Hysteresis
Qualified personnel
Management of Change
Hydrocarbons Safety Conclusions
Hazard is a combination of
A polluted atmosphere
A not proper operation of the vaporizer
Hazard is a combination of
A polluted atmosphere
A not proper operation of the vaporizer
C l d t id t
C l d t id t
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THE GOLDEN RULES
1. Environmental Survey2. Operation of FEP
3. Operation of Vaporizer
4. Deconcentration purge
5. Periodical Deriming
6. Control of the transient phases
7. Control of other sources of pollution
8. EIS management
THE GOLDEN RULES
1. Environmental Survey
2. Operation of FEP
3. Operation of Vaporizer
4. Deconcentration purge
5. Periodical Deriming6. Control of the transient phases
7. Control of other sources of pollution
8. EIS management
Can lead to severe accidentsCan lead to severe accidents
DERIMINGDERIMINGDERIMING
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DERIMINGAND
EXCEPTIONAL REGENERATION
DERIMINGDERIMINGANDAND
EXCEPTIONAL REGENERATIONEXCEPTIONAL REGENERATION
1. Deriming Procedure1. Deriming Procedure Deriming and Drying Procedure
PurposeRemove contaminants in every locations they are subject to
accumulate
Accelerate to warm up of the plant after a shutdown
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Main recommendations
All liquids should be completely purged before starting deriming
Start deriming with all valves closed
6 phases in order to defrost progressively the plant
Proceed from a clean circuit towards a dirty circuit
Use the lowest pressure possible
Keep the deriming outlets wide open
Control the deriming flow rate in order to avoid high velocities
1. Deriming Procedure1. Deriming Procedure
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1. Deriming Procedure1. Deriming Procedure
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2. Exceptional Regeneration2. Exceptional Regeneration
Purpose
Remove impurities not desorbed during regular reactivation
Exceptional procedure to avoid any damage
Carry out :
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Carry out :
At initial start-up
To clean from contaminants accumulated during transportation
To control adsorption capacity respect to design capacityAfter an pollution accident
Late reversal
Liquid water from R02
Unusual temperature at the inlet of the dryers
After repetitive CO2 break-through
2. Exceptional Regeneration2. Exceptional Regeneration
Highlights
Passing dry gas at low pressure and increased temperature
Long period of time through the bottle (24 hours at least)
Temperature in the bottles may range from 230 to 290C
Temperature increase : two steps to avoid damage of
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Temperature increase : two steps to avoid damage ofadsorbents
Outlet electrical heater
Bottle bottom
145C
~120C
~ 240C
290C
Phase 1 Time
Temperature
Phase 2 Phase 3 Phase 4
Effective part of
exceptional regeneration
Effective part of
exceptional regeneration
2. Exceptional Regeneration2. Exceptional Regeneration
ATM
EH-6701
Instrument Air
PV 561
KV 540Deriming Air
From Exchangers
TI
580
Q(WN2) = 121 Nm3/h
P (V-6701 A) = 1.033 bar absTI 513 outlet = 240C
Q(WN2) = 121 Nm3/h
P (V-6701 A) = 1.033 bar absTI 513 outlet = 240C
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C01
V-6701 A V-6701 B
Outlet Water
Inlet Water
To Exchangers
KV 515
ATM
ATM
TI
513
AIR
PERU LNGPERU LNGPERU LNG
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PERU LNGNITROGEN GENERATOR SYSTEM
TRAINING
PERU LNGPERU LNGNITROGEN GENERATOR SYSTEMNITROGEN GENERATOR SYSTEM
TRAININGTRAINING
1. Process description APSA LProcess description APSA L
2. Air Purification Unit2. Air Purification Unit2. 1 Exceptional Regeneration2. 1 Exceptional Regeneration
3. Turbine Expanders3. Turbine Expanders
4. Cold box4. Cold box warm standstillwarm standstill
NITROGEN GENERATOR TRAININGNITROGEN GENERATOR TRAINING
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5. Production5. Production
6. Trip and shutdown6. Trip and shutdown
7. Start up cold standstill7. Start up cold standstill
8. Control loop description8. Control loop description
9. Stutdown9. Stutdown
1. Process description APSA LProcess description APSA L
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PurificationCompression Heat exchange Cold production Distillation
2. Air Purification Unit2. Air Purification UnitTo start it we should do a Initialization; for this the inlet valve should be close and
the inlet pressure PT_502 at 0 bar. You choose the bottle which be in regeneration
and press initialization button. The Bottles will place in HP isolation step.
You open inlet valve FV_580 to pressurize the bottle on line and the HP cold box
Open it to have enough flow for regeneration.
You should open the KV_540 to send air in regeneration bottle and put the PV_561
in auto mode with SP at 160 mbar. When flow from cold box is enough you closeKV 540
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AIR
g yKV_540.
When the timer step is done and you have all condition, a indication Next step
appear you can move manually the sequence by Next step button
If you need to move all the sequence you have a Bypass button to bypass the
heating and cooling timer. But this dont bypass other step.
If all is correct you should put the sequence in auto mode in order to avoid CO2
breakthrough. You can open air production valve FV561 and put in auto SP 750
Nm3/h
In case of problem you must put the sequence in manual mode and check the
problem.
2. Air Purification Unit2. Air Purification Unit1. High Pressure Isolation
Isolation of the bottle in adsorption
Timer step 360s
2. Depressurization
The bottle is slowly depressurized in opposite direction to the adsorption
flow. Drop pressure of bottle should be done during step timer else we
have Depressurization to long and stop the sequence. Timer step 300s
heater
Cold Box
N2cold boxKV_540
Cold Box
N2cold box
heater
KV_540
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KV_520KV_510
KV_526KV_516
KV_525KV_515
KV_530
venting
V-6701A V-6701B
Hp isolationIn service
Ai r
KV_520KV_510
KV_526KV_516
KV_525KV_515
KV_530
venting
V-6701A V-6701B
Hp isolationIn service
Ai r
2. Air Purification Unit2. Air Purification Unit3.Blow-off
Start to send flow thought the bottle. We should have
minimum 8 mbar of DP on heater else Alarm EH-6701
Heater low flow. Timer step 60s
4.Heating
The heater starts to increase temperature at around 150C
In case of the outlet temperature is always < 135c after 15 min Alarm Heater
start fault Timer step 45mn
Cold Box
N2cold box
heater
KV_540