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Areas
of Concern in Cooling Water
Treatment
There
are five primary areas of
concern in recirculating cooling
water treatment: Initial
conditioning, Scale, Fouling,
Corrosion, and Microbiological
control. A successful
cooling water treatment program
must be able to address all five
areas.
1-
Initial Conditioning
A
Proper startup of a
recirculating cooling system
includes chemical conditioning
that provides first, a thorough
cleaning of all metal surfaces,
second, the formation of a
passive protective film on the
metal surfaces, and third,
maintaining the protection of
these metal surfaces.
2-Scale
Scale
is probably the most widely
associated problem in cooling
water systems. This
term has become so generic that
it is often applied incorrectly
to all solid accumulations in
the system. Scale, as
originally defined, forms by
crystallization of a dissolved
salt when its concentration
exceeds its solubility.
Most scale forming compounds
have the unusual property of
becoming less soluble as the
water temperature increases.
Because of this, scale will
generally deposit at the heat of
the exchange surface and water
interface-the very place which
should be kept scale-free for
efficient heat transfer to take
place.
The
most common scale will usually
consist of calcium carbonate.
Its ingredients, calcium and
alkalinity, are present in all
natural water. For any
given water composition and
temperature, the tendency to
form calcium carbonate scale can
be predicted from the
temperature, pH, calcium
hardness, total alkalinity, and
the total dissolved solids
(TDS). This prediction
calculates when a water of known
composition would be in
equilibrium with calcium
carbonate at the indicated
temperature. The
calculation is further
correlated with field experience
data to give a better picture of
what might be expected of a
given water under the specified
conditions. The final answer is
referred to as the Stability
Index. A number below 6.0
indicates scale will form, and
become more pronounced the lower
the index number, while as the
number rises above 7.0, the
water is said to be increasingly
corrosive.
3-
Fouling
Fouling
is the accumulation of solid
material other than scale in a
way that hampers the operation
of plant equipment or
contributes to its
deterioration. Examples of
fouling are:
- Dirt
and silt
- Sand
- Corrosion
Products
- Natural
Organic
- Microbial
Masses
- Aluminum
Phosphates
- Iron
Phosphates
The
most important factors that have
influence over fouling are water
characteristics, temperature,
flow, velocity, microbial
growths, corrosion, and
contamination. Most waters
contain the dissolved and
suspended materials that can
cause a significant fouling
problem under certain
conditions.
As
the temperature increases, the
tendency to foul increases.
Since heat transfer surfaces are
hotter than the cooling water,
they will accelerate the
tendency to foul, and become the
most likely area of fouling.
At
low flow rates (1 foot per
second or less), fouling occurs
due to natural settling of
suspended material. At
higher flow rates (3 feet per
second), fouling can still
occur, but usually is less
severe.
Microorganisms
can form deposits on any
surface. In addition,
corrosive or iron-depositing
bacteria will cause or utilize
corrosion products, which
subsequently deposit as
voluminous foulants. All
microbial colonies act as a
collection site for silt and
dirt, causing a deposit of
different foulants.
Corrosion
can form insoluble corrosion
products that migrate and mix
with debris, process
contamination, or microbial
masses to aggravate fouling.
Material
that leaks from the process side
of heat exchange equipment can
cause serious fouling problems
in several ways:
- Depositing
as insoluble products.
- Providing
nutrients for microorganisms
and causing severe microbial
growths.
- Reacting
with scale or corrosion
inhibitors to form insoluble
foulants
Fouling
can be controlled mechanically
or by the use of a chemical
treatment program.
The best method depends on the
type of fouling present.
Control of fouling in a cooling
water system involves three
steps:
- Prevention
- Whatever can be done to
prevent foulants from
entering the cooling system.
- Reduction
- Steps taken to remove or
reduce the volume of
foulants that unavoidably
enter the system.
Examples would be
side-stream filtering or
periodic cleaning of the
tower basin.
- Problem
Control - Taking regular
action to minimize
deposition of the foulants
in the system. This
would include the use of
specific treatments for
control of fouling, air
bumping or back-flushing of
heat exchangers.
4-Corrosion
Corrosion
is by far the greatest course of
failure of cooling water
equipment. It takes place
to some degree whenever water,
metal and a depolarizing agent
such as oxygen are brought
together. Also, water
inherently contains aggressive
species such as chloride and
sulfate. Corrosion is a
chemical process, therefore, its
rate of reaction will increase
with temperature. In
general, a low pH will increase
the rate of corrosion, while
inhibiting scale. A high
pH will decrease corrosion
and promote scale formation.
Low pH can result from gases
such as sulfur dioxide being
scrubbed from the air by the
cooling tower; acidic process
fluids being leaked in at the
heat exchangers; or an overfeed
of acid, if being used to
control the pH in the cooling
tower.
Non-chemical
factors such as water velocity,
or deposit formation, also play
a considerable role in localized
corrosion, which can accelerate
equipment failures.
Because
corrosion is an electrochemical
process, any condition that
causes one point on a metal
surface to differ from another
will allow a localized corrosion
cell to establish.
Localized corrosion is produced
by crevices, deposits of any
type and local stresses.
Low flow areas can allow
suspended solids to settle out,
and localized corrosion can then
take place under the resulting
deposit. This is one of
the most common causes of
localized corrosion in cooling
water systems.
Another
form of localized corrosion is
galvanic coupling corrosion
caused by the joining of two
different metals in the system.
Galvanic corrosion is well known
and understood, particularly in
the case of copper and steel.
The areas of these different
metals which form the galvanic
cell will also play a part in
the damage caused by corrosion-
A large anodic area (more
corrodible) connected to a small
area of cathodic (more corrosion
resistant) metal is commonly
acceptable because the total
corrosion is spread over a large
area. When the reverse
situation is present, a small
anodic area connected to a large
cathodic area, corrosion will be
accelerated because the
corrosion is concentrated in a
small area which can quickly
lead to the failure of that
area.
When
two metals from this galvanic
series are in contact in
solution, the corrosion rate of
the more anodic (corrodible)
metal increases and the
corrosion rate of the more
cathodic (corrosion resistant)
metal decreases.
5-Microbiological
control
Microbiological
Control is equally important for
a cooling water program to be
successful. Not only will
microbiological fouling impede
heat transfer, it will also set
up a localized corrosion cell.
Biological slimes can allow
anaerobic microorganisms to
thrive, which creates a
localized corrosion cell which
will result in pit type
corrosion. Pitting
corrosion is the most severe
type of corrosion, with the
ability to create holes in
equipment in a short period of
time.
In
evaluating different treatment
programs, one must assume that
good biological control will be
maintained via the use of
appropriate biocides.
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