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