Condensate and Feedwater Corrosion and Treatment
Transcript of Condensate and Feedwater Corrosion and Treatment
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Condensate and Feedwater
Treatment.
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The 3 Main elements associated
with Feedwater treatment arecomponents of Water
H2O Good
O2 Bad
H+
Bad OH- Good (Most of the time)
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Types of Corrosion
General Corrosion - Hematite
Localised Corrosion
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General Corrosion
Hematite Layer
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Localised Corrosion
Pitting O2 plus Cl Often associated withscale deposit
Crevice Corrosion starts in pre-existingcrack or crevice, flanges with porous gaskets
Selective Leaching one element of a multi-element metal
Galvanic Corrosion different metal, differentzones
Stress Corrosion/Stress Cracking
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The principal Contributors to corrosion
in boiler condensate and feedwatersystems are:
Oxygen
Carbon Dioxide
Low pH
Deposits
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Oxygen Corrosion
Oxygen,dissolved in boiler water having
traces of chlorides or solids cancause pitting corrosion of metal
surfaces.
The resulting condition may be
severe, even at low pressure.
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Oxygen and other gases must
be removed from thefeedwater before they can
enter the boiler
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Oxygen Removal
can be accomplishedboth
mechanically and chemically
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A Mechanical means of
removing oxygen is called adeaerator.
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Deaeration
can be eithervacuum or pressure
enhanced.
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The Turbine Condenser
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Deaerating Feedwater Heater
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Boiler Steam/Water Drum
has a role in thedeaeration of the feedwaterat startup.
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Chemical Deaeration
is carried outby the addition of an
oxygen scavenger
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Hydrazine, Carbohydrazide
Theoretical 1mole of Hydrazine will scavenge 1 moleof Oxygen
Usually injected at 3:1 ratio to maintain a residual atentry to the boiler
Hydrazine promotes the formation of a magnetitelayer
Decomposes to form ammonia
Combines with condensate in the condenser to formNaoH
Assists in pH control.
Ammonia is highly corrosive to copper
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CO 2
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Corrosion in steam andcondensate return lines may
be caused by a low pHinduced by carbonic acid
resulting from the associationof CO
2with water.
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A buildup of acidreduces condensate pH
leading to loss of metal andgrooving of the condensate
piping.
( General Corrosion)
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The affect is accelerated in
the presence ofO2
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Volatile, alkaline, neutralising
chemicals are traditionallyused to control low pH.
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Chemicals used to control pH
in the condensate systeminclude:
ammonia
morphaline
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They function only toneutralise
are effective only againstcorrosion initiated by a low
pH
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Neutralising Amines.
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High CO2 levels will demand a greaterquantity of Neutralising Amines
Neutralising Amines are ineffectiveagainst O2
The use of a film forming Amine can be
more effective.
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Filming Amine
A long Chain Molecule having both ahydrophilic and a hydrophobic end.
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The hydrophilic end bonds to themetal forming an adherent, non-
wettable, monomolecular layer ( filmon the metal surface.
Prevents contact between the lowpH condensate and the metalbeneath as well as inhibiting O2attack.
Not really effective where pittinghas occurred
can undercut iron oxide depositscausing rapid removal and possibleproblem associated with steam trapblockage etc.
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Combineduse of the
two aminesprovides amore effective
corrosion control
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By theaddition
of anoxygen scavenger
the regimeis further enhanced.
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Condensate and Feedwater
Polishers
Resin must be suitable for Higher water
temperatures
Pick up metals scale crude etc.
Can be detrimental if they are allowed
to exhaust.
NA and Cl slip.
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Low pHin
Local Areasis the secondmost common
cause of corrosion
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Magnetite
Above 200 Deg C mild steel corrosion results in theformation of magnetite
forms a strongly adherent barrier between the boiler
water and the metal.
Corrosion stops when a uniform layer is formed.
If the layer is disrupted rapid general corrosion canoccur.
Water chemistry must be controlled to maintain thislayer.
pH is maintained > 9.0 , =< 10.5
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Phosphate Control
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Na Hydroxide and Tri Na Phosphate arecommon chemicals used to control pH.
To prevent caustic attack such as
Caustic Gouging the amount of Na hasto be carefully monitored
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Caustic Gouging
Scale is formed by deposit of solid material fromboiler water
This scale is porous
Boiler Water enters the scale and forms a cavity
between the scale and the metal
(Wick Boiling)
continuous operation concentrates the corrosion
product 100ppm TDS - 220,000 ppm Caustic
Corrosion accelerated locally
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Phosphate dosing using either
acoordinated
orcongruent methodis used to control
free Hydrate alkalinity(Caustic)
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Coordinated Method
Boiler Water pH is monitored and kept
below a value responding to a curverelating the pH and Tri Na Phosphate
( Na3Po4 )
Na and PO4 maintained in a ratio of
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Congruent method
Used more commonly in higherpressure boilers
Dosing maintains pH and a ratio of Na :PO4 of 2.6 to 2.8
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Silica
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Silica
High levels of silica form an adherent scale
Above 4Mpa silica begins to volatilise and is
carried over to the after boiler and turbinesections of the plant
Silica can hideout in a boiler at high pressurenot showing up in boiler water analysis andthen redissolving into the boiler water at lowerpressures.
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Maximum silica recommended
2 Mpa 150ppb
4Mpa 40
8Mpa 2
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Hydrogen Embrittlement
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Hydrogen can evolve in a low pHenvironment
If damage to the magnetite layer occurs,It can diffuse into the boiler metal
React with ferrous carbide in the metal
Produce methane
Gas pressure at grain barriers cancause separation
Lowers the carbon content and strengthof the metal
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Stress Cracking
can occur in areas of high tensile stressin the presence of an excess of freealkalinity ( NaOH )
Crack may initiate at an existing flaw orhigh stress point and then begin topropagate as a very fine segregation
line between grain boundaries
Not uncommon above 4Mpa
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Build up of Deposits.
Failure of Heating surfaces.
Deposit Control through Blowdown.
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Equipment Associatedwith Condensate and Feedwater water
Quality Control.
Continuous and Intermittent Blowdown
Hydrazine Dosing System
Amine Dosing System
Phosphate Dosing System
Sampling and Analysis Equipment