Professional Documents
Culture Documents
Text may appear fuzzy or blocky due to file compression. You may be able to change the
appearence (Acrobat Reader 3.x) by going to the menu item File and selecting Preferences,
then General. Click the box next to the item “Smooth text and monochrome images” and
then the OK box at the bottom.
Contents
13.1 Introduction ..................................................................................................................... 2
13.1 Introduction
During the development of any new water treatment project, many equipment issues
have to be addressed. These issues include the capacity, performance, environmental
compliance, capital cost, operating cost, waste volume, and footprint of the water
treatment equipment. In addition to the “hard” equipment issues,“soft” issues such
as customer preferences must also be addressed.
For new water treatment projects, several process areas must be considered,
including pretreatment, demineralization, and condensate polishing (if applicable),
as well as any ancillary components necessary to form a complete system. The
purpose of systems integration is to select the best unit operations that address the
issues identified in the first paragraph and assemble them into a functioning system.
This module provides a brief overview of the most significant factors affecting the
design of a complete water purification system. It is not intended to provide a
definitive discussion of the topic but rather to serve as a starting point for those
without systems integration experience. Any system design should be checked by an
experienced process engineer to ensure that no subtle design issues are overlooked.
The first step in designing a water treatment system is to identify the source of the
water to be treated. This information has a direct bearing on the amount of
pretreatment required and also influences the selection of equipment.
The following list identifies the common sources of feedwater for water treatment
projects:
Once the source of the feedwater has been identified, a complete analysis of the
water must be obtained. To properly analyze the feedwater, samples should be
collected over a period of time, preferably several years. A single sampling is not
effective, as it does not provide the necessary information regarding seasonal
variations in water quality. This information is required so that any variations in the
concentrations of individual ions (or other dissolved or suspended material) can be
accommodated in the system design. A design feedwater analysis is prepared that
presents the water composition that is used to select and size the treatment
equipment.
The composition of well waters is typically more stable than the composition of
surface waters. Well waters generally do not vary significantly over time.
Constituent Analysis in A B C D
ppm as
The effluent quality required from the treatment system is determined by the
intended use of the treated water. For example, boilers that operate at higher
pressures require purer feedwater than those operating at lower pressures. Boiler
manufacturers have water purity specifications that may include conductivity,
sodium, silica, dissolved oxygen, pH, etc.
The flow rate of feedwater required by an application, such as the boiler mentioned
above, depends on the system’s average consumption of water, the peak
consumption rate, the length of the peak, and the amount of storage available. For
example, a boiler requiring a 200-gpm average flow on a continuous basis would
have a different water treatment system than a boiler requiring a 200-gpm average
flow but with 2000-gpm peak consumption rates.
In most applications, the client determines and specifies both the quantity and the
final quality of water required.
The generation and discharge of waste materials are also important considerations
when designing a water treatment system. Various options can be explored
depending on the client’s needs and requirements, for example:
• The use of process equipment that generates less waste such as reverse osmosis,
packed bed ion exchangers, or electrodeionization (EDI) technology
• The application of a rinse recycle step to reduce the waste volume
• The application of combinations of weak and strong ion exchange resins to
reduce chemical usage
• The use of non-regenerable ion exchangers or exchangers that are regenerated
off-site
• The reuse of waste generated by the water treatment system for other in-plant
purposes such as dust suppression or in the scrubber or cooling tower
To select the proper treatment process for any given system, the client’s financial
perspective must also be considered. Some of the non-process factors that influence
equipment selection are:
13.3 Pretreatment
Some examples of impurities that are removed in the pretreatment section of a water
system are TSS, turbidity, color, organics (TOC), iron, and chlorine.
The raw water source heavily influences the choice of pretreatment equipment. The
following sections provide an overview of the variations in equipment design that
may be necessary for four common water supplies: raw surface water, well water, sea
water, and city water.
With the exception of waste water reclamation projects, raw surface water is
generally the poorest quality of water that has to be treated; therefore, it requires the
greatest quantity of pretreatment equipment to make it suitable for treatment by one
of the demineralizing processes.
The potential pretreatment processes that may be employed to treat this type of raw
water are listed below:
The need for an organic scavenger is determined by the type of equipment used in
the downstream demineralization system. If the demineralizing plant includes a
reverse osmosis (RO) unit, the TOC limit would be approximately 3 ppm; however, if
ion exchange is used, the TOC can be no more than 1 ppm. Higher levels of TOC
cause fouling of the downstream equipment and require time consuming cleaning
procedures.
If the downstream equipment is reverse osmosis, activated carbon filters are not
recommended as they can be a source of bacteria and can also pass carbon dust onto
the membranes. Chlorine removal by injection of sodium bisulfite is fast and less
costly than carbon filtration.
Well water normally requires less pretreatment than surface water and also has less
variation in its constituents; therefore, the level of pretreatment required is minimal.
The following list indicates pretreatment processes that can be used for well water:
Sea water is extremely high in dissolved solids (i.e., 30,000 to 40,000 ppm)
depending on the region of the world. It also contains suspended solids, which can
increase dramatically during storms, and, on occasion, oil if the intake is near a
shipping lane.
In the water treatment industry, reverse osmosis with sea water membranes
desalinates the water prior to further purification with brackish water reverse
osmosis membranes. The equipment used to pretreat the sea water upstream of the
RO is listed below:
Possible treatment processes are listed below. All of these must be evaluated based
on the quality and constituents of the city water.
The demineralization section of the water treatment system is where the ionic
content, or total dissolved solids (TDS), of the water is reduced to the levels required
by the user.
The TDS of the raw water and the quality of treated water required influence the
process equipment selection. Some examples of equipment selections are listed
below to show the complexities that can be encountered.
13.4.1 Low Pressure Boilers and Light Industrial Applications, e.g., Laundries
Simple softening can produce water for this service. The residual hardness level will
determine the type of softener that should be used. The options are as follows:
• Reverse osmosis followed by a decarbonator and mixed bed ion exchange: This
produces treated water with an average of 1 µS/cm conductivity and 10 to 20 ppb
silica.
For this application, the highest water quality is required to prevent scaling of the
boiler tubes and turbine blades. To achieve higher quality, a polishing demineralizer
is added to the process equipment arrangement. The polishing demineralizer can be
a mixed bed, a polishing cation exchanger, or an electrodeionization unit. The
following equipment examples indicate the range of systems that can be provided to
produce high quality demineralized water.
• Reverse osmosis followed by decarbonation and mixed bed ion exchange. This
produces treated water with an average of 1 µS/cm conductivity and 10 to 20 ppb
silica. The RO is normally a single pass design; however, a double pass RO
system could be used to increase the run length of the mixed bed.
Any of the above systems that use two-bed demineralizers could be changed to four-
bed systems with weak and strong resins in the cation and anion exchangers if the
composition of the raw water is suitable.
Condensate, which is steam that has condensed back to water after giving up its
heat, can be reused in a boiler. Condensate picks up ionic contaminants from
cooling water in-leakage and condenser leakage, along with corrosion products such
as iron and copper oxides.
In some applications, the condensate is returned from a steam host that uses the
steam in the manufacturing process. In such cases, the condensate may contain
other contaminants picked up from the product (e.g., pulp fiber from a paper mill).
These contaminants must also be removed before the condensate can be reused.
There are several different types of condensate polishers. A brief summary of the
available types is given below (Module 10 has complete details).
• Sodium cycle polisher: This is a cation only polisher that is used to polish
condensate at temperatures up to 275o F in applications for which silica reduction
is not a concern. This type of polisher removes trace hardness ions in exchange
for sodium ions and also filters out particulate matter.
• Amine cycle polisher: This is also a cation only polisher that is used to polish
condensate at temperatures up to 275o F in applications where silica reduction is
not a concern but where the addition of sodium is not acceptable. This type of
polisher removes trace hardness ions in exchange for amine ions and also filters
out particulate matter.
• In-situ regenerated deep bed polisher: This is a mixed bed polisher used in-line
(full flow polisher) or side-stream (partial flow polisher), at temperatures up to
120oF but preferably not higher than 100oF (to control silica leakage). This type of
polisher has a potential for leakage of regenerant into the process stream. It also
has a higher degree of cross-contamination and therefore produces lower quality
treated condensate than that produced by externally regenerated polishers.
• Externally regenerated deep bed polisher: This is also a mixed bed polisher used
in-line or side-stream, at temperatures up to 120oF but preferably not higher than
100oF (to control silica leakage). These units are normally found in central
utilities such as nuclear power plants for which the highest quality is required,
particularly for supercritical boilers.
The following examples are intended to represent the types of systems used in
modern water treatment systems. They show typical processes, based on the type of
raw water source, the water analysis, and the required performance guarantee. It
must be stressed that each new system must be selected or designed based on the
prevailing water analysis and the “hard” and “soft” parameters dictated by the
prospective client. There may be more than one “right” answer to a design problem,
and there may be subtle conditions that shift the preference from one design to
another.
Water Analysis
Carbon Dioxide 10
Silica 20
TEA 822
Other Contaminants
pH 10.4
TSS 50 ppm
Temperature 104oF
Recommended Equipment
Multi-media filter
Co-current strong acid cation exchanger
Co-current strong base anion exchanger
Selection Factors
1. The high level of TSS in the raw water requires the use of filtration. Since iron and
chlorine are not present, multi-media filtration is selected.
2. The required effluent quality is not particularly stringent and can be achieved using a
basic two-bed demineralizer, which is simple to operate and maintain and which is also
low in capital cost.
3. The client has prior experience with similar equipment.
Comments
• At first glance, the TDS in the raw water would suggest the use of RO instead of ion
exchange; however, the reported water temperature is already at the maximum operat-
ing temperature for RO membranes. Therefore, ion exchange is selected.
Water Analysis
Selection Factors
1. The very low level of TDS in the feedwater makes this water ideal for treatment by ion
exchange.
2. The required treated water quality indicates a need for final polishing using a mixed bed.
3. The client requires filtration before the ion exchange beds.
4. The free chlorine level is greater than 0.2 ppm and must be reduced. A bisulfite feeder
is selected as the most cost-effective method.
Comments
• As an alternative to the sodium bisulfite feeder and cartridge filtration, activated carbon
filtration could be used; however, this would increase the capital cost and require more
floor space.
• The cartridge filter is not indicated by the feedwater data (since particulate matter can be
backwashed out of a co-current ion exchange unit), but the client is concerned about
particulate loading.
• Other forms of ion exchange could be used, such as a packed two-bed system (cation
and anion exchangers) with a high flow cation polisher. This choice would simplify the
operation and possibly reduce the capital cost of the plant; however, the client prefers
the more traditional approach of using a mixed bed demineralizer.
Carbon Dioxide 25
Silica 5
TEA 266
Other Contaminants
pH 7.0
Organics 10 ppm TOC
Turbidity 7 NTU
Temperature 35 to 85oF
Performance Guarantee
Conductivity 1 mmho/cm
Sodium 0.03 ppm as CaCO3
Silica 0.1 ppm as CaCO3
Equipment Selection
Multi-media filter
Sandwich packed bed weak/strong acid cation exchanger
Forced draft decarbonator
Sandwich packed bed weak/strong base anion exchanger
Selection Factors
1. Because the feedwater turbidity is greater than 1 NTU, filtration is required. No iron or
chlorine is present, so multi-media filtration is selected as the least costly alternative.
2. The analysis favors the use of weak cation resin since there is a substantial quantity of
hardness in the water and a reasonable ratio of hardness to alkalinity. The weak resin is
very chemically efficient and greatly reduces the ionic load that the strong resin must
subsequently remove.
3. A forced draft decarbonator is required since more than 50% of the feed to the anion
exchanger is carbon dioxide. By removing this carbon dioxide, the decarbonator
reduces the volume of strong base resin needed in the anion exchanger and also
reduces the use of caustic.
4. The load on the anion resin is 89% mineral acids and only 11% weak acids. This strongly
suggests the use of weak base anion resin to improve chemical efficiency.
5. An additional factor in selecting weak base anion resin is the presence of up to 10 ppm
of TOC. This high concentration would quickly foul any strong base resin and is also
much higher than any weak resin can handle on a consistent basis. Adjusting the perfor-
mance of the clarifier should control this high level of TOC.
6. Counter current regeneration of the strong ion exchange beds is required to achieve the
required quality of treated water.
Water Analysis
Performance Guarantee
Conductivity 0.25 mmho/cm
Sodium 0.02 ppm as Na
Silica 0.01 ppm as CaCO3
TDS 0.04 mg/l as CaCO3
Iron 0.01 mg/l as Fe
Copper 0.01 mg/l as Cu
Equipment Selection
Manganese greensand filtration with potassium permanganate (KmnO4) feed
Organic scavenger
Acid feed system
Antiscalant feed system
RO prefilter – 5 micron nominal
Single pass RO
Forced draft decarbonator
Mixed bed exchanger
Comments
• Particular attention must be paid to the pretreatment upstream of the reverse osmosis
unit due to the presence of iron, barium, H2S and substantial amounts of TOC. The
greensand filters remove iron, manganese, TSS and possibly some of the color (TOC).
• The analysis reports less than 0.1 mg/l of H2S in the feed. This probably means that the
concentration of H2S is below the detection limit of the laboratory performing the
analysis. If H2S is present, it would preclude the use of any oxidizing agents, since they
would convert the H2S into elemental sulphur that plugs up filters and RO membranes.
• To reduce the scaling potential of the feedwater, acid is fed upstream of the RO to lower
the LSI to a negative value. The acid injection, in turn, converts some of the bicarbonate
ions to carbon dioxide, which is not removed by the RO. This carbon dioxide would very
quickly exhaust the mixed bed were it not for the decarbonator that reduces the CO2 to
between 5 and 10 ppm at the mixed bed inlet.
• The very high level of reactive silica in the feedwater requires the addition of an
antiscalant specifically designed to prevent silica scaling (e.g., ARGO SI300).
Water Analysis
Carbon Dioxide 2
Silica 10.5
TEA 591.5
Other Contaminants
pH 7.5 to 8.3 Barium 0.08 mg/l
Organics 1 ppm TOC Iron 0.13 mg/l
Turbidity 1 NTU Manganese 0.01 mg/l
Temperature 36 to 77oF Aluminum 0.3 mg/l
Free Chlorine 0.12 mg/l SDI 5
Performance Guarantee
Conductivity 0.1 mmho/cm
Sodium 0.01 ppm as Na
Silica 0.02 ppm as SiO2
TDS 0.2 mg/l
Equipment Selection
Acid feed system
Antiscalant feed system
Sodium bisulfite feed system
RO prefilter – 5 micron nominal
Single pass reverse osmosis
Forced draft decarbonator
E-CellTM electrodeionization unit
Selection Factors
1. The level of suspended solids (indicated by turbidity) in the feedwater does not justify
the addition of media filtration; therefore, only conventional cartridge filtration is pro-
vided upstream of the RO.
2. RO is selected as the roughing demineralizer due to the moderately high TDS of the
feedwater.
3. A forced draft decarbonator is required to remove the carbon dioxide generated by the
addition of acid upstream of the RO.
4. To achieve the required treated water quality, a mixed bed ion exchanger or EDI unit is
required. EDI is selected to reduce the onsite storage and handling of chemicals.
Water Analysis
Carbon Dioxide 9
Silica 26
TEA 35411
Other Contaminants
pH 8.1 to 8.3
Temperature 78 to 91oF
Performance Guarantee
Conductivity 0.25 mmho/cm
Sodium 0.05 ppm as CaCO3
Silica 0.02 ppm as SiO2
Equipment Selection
Coagulant feeder
Coagulant aid feeder
Primary multi-media filtration
Polishing multi-media filtration
Acid feeder
Antiscalant feeder
Sodium bisulfite feeder
RO prefilter – 5 micron nominal
Single pass sea water reverse osmosis
Forced draft decarbonator
Brackish water reverse osmosis
Mixed bed demineralizer
Comments
• Ultrafiltration could have been used instead of media filtration for the pretreatment of
the seawater. This would have resulted in lower operating costs but higher capital costs.
• Thermal evaporation could have been used in place of the seawater RO, but in this case
thermal evaporation has higher capital and operating costs.
• Since an RO is being used, sodium bisulfite is the preferred method of chlorine removal.
The membranes have a chlorine tolerance of 1000 ppm hours.
• To reduce the scaling potential of the feedwater, acid is fed upstream of the RO to lower
the LSI to a negative value. This, in turn, converts some of the bicarbonate ions to
carbon dioxide, which is not removed by the RO. The carbon dioxide would very quickly
exhaust the final ion exchanger were it not for the decarbonator that reduces the level of
carbon dioxide in the feed to 5 ppm.
• An antiscalant is fed upstream of the RO as additional protection against scaling.
• The permeate from the sea water RO is still high in TDS, (approximately 500 ppm);
therefore, a second RO pass is required prior to final demineralization.
• The final water quality can be met using either conventional mixed bed ion exchange or
EDI technology. Since chemicals are already being used for other parts of the plant
(e.g., condensate polishing), the conventional approach is desirable.
Water Analysis
Conductivity 10 to 15 mmho/cm
Hardness 5 to 7.5 ppm as CaCO3
Iron 0.1 to 0.2 mg/l as Fe
Copper 0.02 to 0.1 mg/l as Cu
pH 8.0 to 8.5
Temperature 180 to 210oF
Performance Guarantee
Hardness 0.1 ppm as CaCO3
Iron 0.02 ppm as Fe
Equipment Selection
Sodium cycle condensate polishers
Selection Factors
1. Since the operating temperature is very high and no silica reduction is required, a simple
sodium cycle cation polisher is the process of choice.
Comments
• An amine cycle polisher could also be used for this application; however, the client has
no concerns about the sodium content of the treated condensate.
Water Analysis
Total non-volatile
dissolved solids 50 ppb
Suspended
Solids 20 ppb
Ammonia 800 to 1200 ppb as CaCO3
Iron 10 ppb as Fe
Copper 5 ppb as Cu
Silica 20 ppb as SiO2
Sodium 5 ppb as CaCO3
Chloride 5 ppb as CaCO3
Temperature 90 to 120oF
Performance Guarantee
TDS 25 ppb
TSS 10 ppb
Cation Conductivity 0.1 mS/cm
Total Iron 5 ppb as Fe
Total Copper 2 ppb as Cu
Silica 5 ppb as SiO2
Sodium 1 ppb as Na
Chloride 2 ppb as Cl
Equipment Selection
Externally regenerated mixed bed condensate polishers
Selection Factors
1. The required performance guarantee requires the use of a mixed bed condensate
polisher.
Comments
• To maintain the low levels of cross-contamination required by this process, external
regeneration of the mixed bed condensate polisher is used.