Boiler Tube Failures: Pradip Patel
Boiler Tube Failures: Pradip Patel
Boiler Tube Failures: Pradip Patel
Mentor:
Pradip Patel
Submitted by:
Vishnu Parvanda
Saiyam Goyal
Cationic Anionic
Nonionic and undissolved Gases
Calcium
Bicarbonate Turbidity, silt, mud
CO2
Magnesium Carbonate
H2S
Hydroxide
NH3
Sodium
Color, Plankton
CH4
Potassium Sulfate
Organic matter,
O2
Ammonium Chloride
Colloidal silica,
Iron
Nitrate
Microorganisms,
Manganese Phosphate
Bacteria
Waterwalls
Furnace wall that is comprised of refractory and tubes in a
water tube boiler. Tubes are evenly spaced and generally
connect to headers which in turn are connected back to drum
of boiler.
Absorb 50% of heat released by combustion of fuel in furnace.
Mixture of steam and water discharged from top of these
tubes into upper wall header and ten passes through riser
tubes to steam drum.
Types:
Tangent tube construction
Membrane wall construction
Exfoliation
Stresses imposed on SH and RH tubes will
eventually cause cracks in the magnetite layer that
forms on internal wall surfaces..
Pieces of iron oxide will break off and will be carried
by steam to turbine. Pieces that are small enough to
pass through turbine screens impinge upon the
turbine blades and cause physical damage.
This problem is more acute in cycling units because
frequent startups, shutdowns or load changes
Deposition
Deposits refers to materials that originate elsewhere
and are conveyed to a deposition site.
Boiler deposits come from four sources: water borne
minerals, treatment chemicals, corrosion products
( preboiler and boiler), and contaminants.
Deposits from these sources may interact to increase
deposition rates, to produce a more tenacious layer,
and to serve as nucleation sites for deposit formation.
Such species include metal oxides, copper,
phosphates, carbonates, silicates, sulfates, and
contaminants, as well as a variety of organic and
inorganic compounds.
Mechanism
One deposition process involves the
concentration of soluble and insoluble species in
a thin film bordering the metal surface during
steam-bubble formation. Material segregates at
the steam/water interface, moves along the
interface, and is deposited at the bubble base as
the bubble grows.
Critical Factors
The tendency to form deposits is related to localized heat
input, water turbulence, and water composition at
or near the tube wall.
When a steam bubble becomes dislodged from a tube wall,
the deposits are washed with water. The rate at which the
deposit builds depends on the rate of bubble formation and
the effective solubility of the deposit.
In cases of high heat input, a stable steam blanket can form
and cause concentration of water soluble material.
The rate at which deposits form on heat-transfer surfaces is
controlled mainly by the solubility and physical
tenacity of the deposit and the amount of water washing
that occurs on deposition site.
Iron oxides
A smooth, black, tenacious, dense magnetite layer naturally grows on
steel under reducing conditions found on boiler water-side surfaces.
Magnetite forms by direct reaction of water with the tube metal. In
higher pressure boilers, the magnetite contains two layers.
Particulate iron oxide can deposit on top of the smooth, thermally
formed magnetite layer if settling rates are high and/or if steaming is
appreciable. Usually, coarse, particulate magnetite will not
tenaciously adhere to surfaces unless intermixed with other deposits.
Hematite formation, is favored at lower temperatures and higher
oxygen concentrations. Hematite is a binder species that tends to
accumulate and hold other materials in the deposit. Hematite can be
red if formed where oxygen concentrations are high.
Salts
The least soluble compounds deposit first when boiling occurs.
Calcium carbonate deposits quickly, forming a white, friable
deposit.
Calcium sulfate requires a higher degree of concentration to
deposit than carbonate.
Magnesium phosphate is a binder that can produce very hard,
adherent deposits. Most magnesium phosphate deposits are colorless
but become red, brown, or black when contaminated with iron oxides.
Insoluble silicates are present in many boilers. Many silicates are
very hard and are almost insoluble in acids except for hydrofluoric.
Complex silicates such as analcite (Na2O Al2O3 4SiO2 2H2O),
acmite (Na2O Fe2O3 4SiO2), or sodalite [Na2O 3Al2O3 SiO2
2NaCl] can be evidence for steam blanketing,.
Corrosion
Corrosion is one of the main causes of reduced
reliability in steam generating systems.
Many corrosion problems occur in the hottest areas
of the boiler-the water wall, screen, and superheater
tubes. Other common problem areas include
deaerators, feedwater heaters, and economizers.
The most common causes of corrosion are
dissolved gases, under-deposit attack, low
pH, and attack of areas weakened by mechanical
stress, leading to stress and fatigue cracking.
Acidic Corrosion
Due to presence of CO in condensate water.
Feed water can also become acidic from contamination of
the system (process contamination of condensate or cooling
water contamination from condensers).
Acidic corrosion can also be caused by chemical cleaning
operations (overheating of the cleaning solution, excessive
exposure of metal to cleaning agent, high cleaning agent
concentration).
In the boiler and feed water system, acidic attack can take the
form of general thinning, or it can be localized at areas of
high stress.
O Pitting
Oxygen in water produces pitting that is very severe
because of its localized nature.
Water containing ammonia, particularly in the presence of
oxygen, readily attacks copper and copper bearing alloys.
Oxygen corrosion may be highly localized or may cover
an extensive area.
Most common attack site is in the super heater tubes.
Moisture condensing on the walls of an idle super heater
tube will dissolve atmospheric oxygen.
Oxygen pits can act as stress-concentration sites,
thereby fostering the development of corrosion-fatigue
cracks, caustic cracks, and other stress-related failures.
Caustic Corrosion
Caustic corrosion is confined to
(1) water-cooled tubes in regions of high heat flux,
(2) slanted or horizontal tubes,
(3) locations beneath heavy deposits, and
(4) heat-transfer regions at or adjacent either to backing
rings at welds or to other devices that disrupt flow.
()Corrosive interaction of sufficiently concentrated
sodium hydroxide with a metal to produce distinct
depressions
()At times, a crust of hard deposits and corrosion
products containing magnetite crystals will surround
and/or overlie the attacked region.
Oxides of iron are corroded by both low-pH and highpH environments. High-pH substances, such as
sodium hydroxide, will dissolve magnetite:
4NaOH + FeO 2NaFeO + NaFeO + 2HO
With the protective covering destroyed, water is then
able to react directly with iron to evolve atomic
hydrogen:
3Fe + 4HO FeO + 8H
When magnetite is removed, the sodium hydroxide
may react directly with the iron:
Fe + 2NaOH NaFeO + H
Critical factors
Two contribute to caustic corrosion. The first is
the availability of sodium hydroxide or of
alkaline-producing salts.
The second contributing factor is the mechanism
of concentration.
Three basic concentration mechanisms exist:
1. Departure from nucleate boiling (DNB).
2. Deposition
3. Evaporation at a waterline
Prevention
The following remedies may eliminate corrosion that
depends on the availability of sodium hydroxide or
alkaline-producing salts:
Reduce the amount of available free sodium
hydroxide.
Prevent inadvertent release of caustic regeneration
chemicals from makeupwater demineralizers
Prevent in-leakage of alkaline-producing salts into
condensers
Hydrogen corrosion
Result of electrochemical corrosion reactions in which hydrogen in
the atomic form is liberated.
Two critical factors govern susceptibility to hydrogen damage. These
are the availability of high- or low-pH substances, and a mechanism
of concentration. Both must be present simultaneously for hydrogen
damage to occur.
Ex. Concentrated sodium hydroxide dissolves the magnetic iron
oxide according to the following reaction:
4NaOH + FeO -2NaFeO + NaFeO + 2HO
With the protective covering destroyed, water is then able to react
directly with iron to evolve atomic hydrogen:
3Fe + 4HO FeO + 8H
The sodium hydroxide itself may also react with the iron to produce
hydrogen:
Fe + 2NaOH NaFeO + 2H
Erosion
Erosion is metal loss caused by impact of solids or liquids.
Attack is promoted by turbulent, high-velocity fluid flow. Rapid
pressure changes promote water jetting and turbulence. Abrupt
changes in flow direction and the entrainment of hard
particulate matter in fluids also contribute to wastage.
Feedwater-pump components, including impellers, fittings,
valves, and housings are often eroded. Less commonly, transfer
lines, pipe elbows, and blowdown components are attacked.
Afterboiler erosion is confined primarily to turbines. Because of
high velocities inherent in turbine operation, turbine
components frequently suffer erosion. Turbine blades are
wasted both by hard particles and by water-droplet
impingement.
Critical Factors
Factors controlling the rate of metal loss are related to
the quantity, impact angle, speed, and density of the
erodent. Metal loss is a strong function of erodent
kinetic energy.
Erosion damage maybe roughly considered inversely
proportional to alloy hardness. Usually, in the absence
of significant corrosion, the harder the alloy, the more
resistant it will be to attack.
Erodent velocity has a very important effect on metal
loss. Doubling velocity may increase metal loss by a
factor of 4 or more.
Sample Conditioning:
The Sample is First cooled in Sample Coolers,
depressurized in pressure regulators and
then fed to various analyzers while keeping the
flow characteristics constant by means of a
Back Pressure Regulating Device.
Sample Filter
Any particle of size up to 40 microns size
can be filtered out
Resin Column
The cation conductivity
measurements are considered to be
more reliable than ordinary
conductivity measurements, as this
method ensures elimination of
masking effects of desired chemicals
used in treating the water.
This provides a more realistic
picture of dissolved impurities in the
sample.
pH Analyzer
The pH value of the feed water gives direct indication
of alkalinity or acidity of this water.
In steam circuit it is normal practice to keep the pH
value of feed water at slightly alkaline levels. This
helps in preventing the corrosion of pipe work and
other equipment.
Typically dedicated pH Analyzers are recommended at
following locations in Steam circuit: High pressure
heaters, DM Make-up Water, Condensate Extraction
Pump Discharge
Conductivity
Conductivity is an important parameter for detecting
any contamination of steam in the boiler circuit.
Conductivity of pure water is almost zero (1-2 S). Even
addition of 1 ppm of salt may increase conductivity >
100 S. Thus conductivity is an important parameter
for the detection of leakages.
Typical points in the steam circuit where conductivity
should be monitored are . Superheated steam, Drum
water, High pressure heaters, Low pressure heaters,
Condenser, Plant effluent, D.M. plant, Make-up water
to D.M. plant
Silica(SiO)
The solubility of silica in stream
increases with pressure.
The presence of silica in the steam
can lead to deposition in
superheated tubes and on the
turbine blades which may lead to
loss of efficiency and turbine blade
failure.
For proper working of turbines,
continuous monitoring of silica is
highly recommended.
DO
Hydrazine(NH)
Hydrazine is used as oxygen scavenger and
for maintaining feed water alkalinity to
prevent acidic corrosion.
The nominal dosage rate for hydrazine in
feed water is about three times its oxygen
level. Under dosing of hydrazine leads to
increased corrosion; overdosing represents
a costly waste. Therefore hydrazine
monitoring is extremely important.
The typical points in steam circuit where
hydrazine monitoring is required are. Reheaters, Economizer inlet and L.P. heaters.
Screening
Pre Chlorination
Aeration
Softening
Coagulation
Flocculation
Clarification
Membrane separation
Filtration
Thank You!!!