PSD CEU 201july13
PSD CEU 201july13
PSD CEU 201july13
Treatment
CEU 201
Continuing Education from the
American Society of Plumbing Engineers
July 2013
ASPE.ORG/ReadLearnEarn
READ, LEARN, EARN
Note: In determining your answers to the CE questions, use only the material presented in the corresponding continuing education
article. Using information from other materials may result in a wrong answer.
tion. No single filtration or treatment process satisfies Calcium carbonate Chalk, limestone, marble CaCO 3
all water-conditioning requirements. Calcium hypochlorite Bleaching powder, chloride of lime Ca(ClO)2
Surface water may contain more of these con- Chlorine (gas) — Cl2
Calcium sulfate — CaSO4
taminants than groundwater, but groundwater, while
Calcium sulfate Plaster of paris CaSO4.½H2O
likely to contain less pathogens than surface water,
Calcium sulfate Gypsum CaSO4.2H2O
may contain dissolved minerals and have undesirable Carbon Graphite C
tastes and odors. Water provided by public and private Carbonate (ion) — CO32-
utilities is regarded to be potable, or adequately pure Carbon dioxide — CO2
for human consumption so long as it meets the stan- Ferric oxide Burat ochre Fe2O3
dards of the U.S. Environmental Protection Agency’s Ferruous carbonate — FeCO3
Safe Drinking Water Act and the local health official. Ferrous oxide — FeO
However, such water still might contain some levels Hydrochloric acid Muriatic acid HCl
of pathogens and other undesirable components. Even Hydrogen (ion) — H+
if the water quality would not cause a specific health Hydrogen (gas) — H2
threat to the general public, it may not be suitable for Hydrogen sulfide — H 2S
buildings such as hospitals and nursing homes that Iron (ferric ion) — Fe 3+
house populations that may be vulnerable. Moreover, Iron (ferrous ion) — Fe2+
Magnesium bicarbonate — Mg(HCO3)2
it may not be pure enough for certain industrial, medi-
Magnesium carbonate Magnesite MgCO3
cal, or scientific purposes.
Magnesium oxide Magnesia MgO
Impure water damages piping and equipment by Magnesium sulfate — MgSO4
scoring, scaling, and corroding. Under certain condi- Magnesium sulfate Epsom salt MgSO4.7H2O
tions, water containing particles in suspension erodes Manganese (metal) — Mn
the piping and scores moving parts. Water containing Methane Marsh gas CH4
dissolved acidic chemicals in sufficient quantities Nitrogen (gas) — N2
dissolves the metal surfaces with which it comes Oxygen (gas) — O2
in contact. Pitted pipe and tank walls are common Potassium (metal) — K
manifestations of the phenomenon called corrosion. Potassium permanganate Permanganate of potash KMnO4
Scaling occurs when calcium or magnesium com- Sodium (metal) — Na
pounds in the water (in a condition commonly known Sodium bicarbonate Baking soda, bicarbonate of soda NaHCO 3
as water hardness) become separated from the water Sodium carbonate Soda ash Na 2CO 3
and adhere to the piping and equipment surfaces. This Sodium carbonate Sal soda Na2CO3.10H2O
Sodium chloride Salt NaCl
separation is usually induced by a rise in temperature
Sodium hydroxide Caustic soda, lye NaOH
because these minerals become less soluble as the
Sodium sulfate Glauber’s salt Na2SO4.10H2O
temperature increases. In addition to restricting flow, Sulfate (ion) — SO42–
scaling damages heat-transfer surfaces by decreasing Sulfuric acid Oil of vitrol H2SO4
heat-exchange capabilities. The result of this condition Water — H2O
is the overheating of tubes, followed by failures and
equipment damage.
by adding chemicals to the water as it enters the equipment
Changing the chemical composition of the water by means
is referred to as internal treatment. Economic considerations
of mechanical devices (filters, softeners, demineralizers, de-
usually govern the choice between the two methods. Some-
ionizers, and reverse osmosis) is called external treatment
times it is necessary to apply more than one technology. For
because such treatment is outside the equipment into which
instance, a water softener may be required to treat domestic
the water flows. Neutralizing the objectionable constituents
Reprinted from Plumbing Engineering Design Handbook, Volume 4. © 2012, American Society of Plumbing Engineers.
Table 10-2 Water Treatment—Impurities and Constituents, Possible Effects and Suggested Treatments
Possible Effectsa Treatment
filtration, evaporation, ion
Neutralizing, followed by
chemicals, ion exchange
softening or evaporation
ion exchange materials,
Softening by chemicals,
demineralization by ion-
materials, evaporatiors
Coagulation, filtration,
filtration, evaporation
Softening by heaters,
Setting, coagulation,
Setting, coagulation,
exchange material
Evaporation and
Embritlement
None (Inert)
evaporators
evaporation
De-aeration
exchange
Corrosion
Priming
Foamin
Sludge
Scale
Suspended solids X X X X X
Silica — SiO2 X X
Calcium carbonate — CaCO3 X X
Calcium bicarbonate — Ca(HCO3)2 X X
Calcium Sulfate — CaSO4 X X X
Calcium chloride — CaCl2 X X
Magnesium carbonate — MgCO3 X X
Constituents
Notes: The turbid water enters the central uptake mixed with the coagulant and is forced
toward the bottom of the unit. Some water and the suspended precipitates enter the lower
end of the uptake for recirculation and contact with the incoming chemicals and the water.
New coagulation is encouraged by contact with these previously formed precipitates. The
water then enters the outer settling section. The clarified water rises to the outlet flume
above. The heavier particles settle and are moved along the bottom to the sludge pit.
Figure 10-4 Mechanical Clarifier Figure 10-5 Rectangular Gravity Sand Filter
JULY 2013 Read, Learn, Earn 9
READ, LEARN, EARN: Water Treatment
purity of the effluent water at all times. This instrument is change units are operated in parallel, and their effluents are
essentially a meter for measuring the electrical resistance of combined. Mineral acids in the hydrogen ion exchange efflu-
the treated water leaving the unit. It consists of two principal ent neutralize the bicarbonates in the sodium ion exchange
parts: the conductivity cell, which is situated in the effluent effluent. The proportions of the two processes are varied to
line, and the instrument box to which the conductivity cell produce a blended effluent having the desired alkalinity. The
is connected.
The conductivity cell contains two electrodes across
which an electric potential is applied. When these poles are
immersed in the treated water, the resistance to the flow of
the electricity between the two poles (which depends on the
dissolved solids content of the water) is measured by a circuit
in the instrument. The purity of the water may be checked
by reading the meter. When the purity of the water is within
the specific limits, the green light glows. When the water
becomes too impure to use, the red light glows. In addition,
a bell may be added that rings when the red light glows to
provide an audible as well as a visible report that the unit
needs regeneration. This contact also can close an effluent
valve, shift operation to another unit if desired, or put the
unit into regeneration.
Controls
Several types of controls are currently available to carry out
the various steps of regeneration and return to service. The Figure 10-6 Vertical Pressure Sand Filter
two most common arrangements follow:
• Type A: This consists of completely automatic, individual
air- or hydraulic-operated diaphragm valves controlled
by a sequence timer, and regeneration is initiated via a
conductivity meter. This arrangement provides maxi-
mum flexibility in varying amounts and concentrations
of regenerants, length of rinsing, and all other steps of
the operating procedure. The diaphragm valves used are
tight seating, offering maximum protection against leak-
age and thus contamination with minimal maintenance.
• Type B: This consists of manually operated individual
valves. This system combines maximum flexibility and
minimal maintenance with an economical first cost. It
typically is used on larger installations.
Internal Arrangements
The internal arrangements of the vessels are similar for all
types of controls. The internal arrangement used on me- Figure 10-7 Backwashing
dium to large units is shown in Figure 10-13. Smaller units
have simpler arrangements since the distribution problems
are less complex. The positive and thorough distribution of
regenerants, rinse, and wash waters to achieve maximum
efficiency provides economy and reliability.
Ion Exchange Water Softeners
A typical hydrogen-sodium ion exchange plant is shown
in Figure 10-14. This process combines sodium-cycle ion
exchange softening with hydrogen-cycle cation exchange.
The sodium ion exchange process is exactly the same as a
standard ion exchange water softener. The hardness (calcium
and magnesium) is replaced with sodium (non-scaling). The
alkalinity (bicarbonates) and other anions remain as high
as in the raw water.
The cation exchanger is exactly the same as the one used
with demineralizers; therefore, its effluent contains carbonic
acid, sulfuric acid, and hydrochloric acid. Sodium ion ex-
Figure 10-8 Filtration and Backsplash Cycles
10 Read, Learn, Earn JULY 2013
carbon dioxide is removed by a degasifier. The effluent is soft, frequency of regeneration, single versus multiple systems,
low in solids, and as alkaline as desired. space requirements, cost, and operating efficiency.
In the sodium ion exchange softener plus acid addition
Flow Rate
process (see Figure 10-15), the acid directly neutralizes the
After determining the total flow rate requirements for the
bicarbonate’s alkalinity to produce a soft, low-alkaline water.
building, including all equipment, the engineer can consider
The carbon dioxide produced is removed by a degasifier. The
the size of the water softener. The unit selected should not
chief disadvantages of this process are that the total dissolved
restrict the water flow rate beyond the pressure loss that the
solids are not reduced and control of the process is difficult.
building can withstand, based on the pressures available at
In a sodium ion exchange softener plus chloride deal-
the source and the minimum pressure needed throughout
kalizer process, water passes first through the sodium ion
the entire system. A water softener that meets both flow rate
exchange softener, which removes the hardness, and then
and pressure drop requirements should be selected.
through a chloride dealkalizer, which is an ion exchanger that
operates in the chloride cycle. The bicarbonates and sulfates
are replaced by chlorides. The resin is regenerated with
sodium chloride (common salt). The equipment is the same
as that for sodium ion softeners. This process produces soft,
low-alkaline water. Total dissolved solids are not reduced, but
the chloride level is increased. The chief advantages of this
process are the elimination of acid and the extreme simplicity
of the operation. No blending or proportioning is required.
In some cases, the anion resin can be regenerated with
salt and caustic soda to improve capacity and reduce the
leakage of carbon dioxide.
Water Softening
Water softening is required for practically all commercial and
industrial building water usage. Generally speaking, almost
any building supplied with water having a hardness of 3.5 Figure 10-9 Mudballs
grains per gallon (gpg) or more should have a water softener.
This is true even if the only usage of the water other than
for domestic purposes is for heating because the principal
threat to water heater life and performance is hard water.
Approximately 85 percent of the water supplies in the United
States have hardness values above the 3.5 gpg level.
However, it is not good practice to specify a water softener
to supply the heating equipment only and disregard the
softening needs for the balance of the cold water usage in
the building. A typical example of this condition is a college
dormitory. Many fixtures and appliances in a dormitory in
addition to the hot water heater require soft water, includ-
ing the piping itself, flush valve toilets, shower stalls, basins,
and laundry rooms. Many fixtures and appliances that use
a blend of hot and cold water experience scale buildup and
staining, even when the hot water is softened. Figure 10-10 Fissures
One of the most common reasons for installing water
softening equipment is to prevent hardness scale buildup in
piping systems, valves, and other plumbing fixtures. Scale
builds up continually and at a faster rate as the temperature
increases. The graph in Figure 10-16 illustrates the degree
of scale deposit and the rate increase as the temperature of
the water is elevated on water having a hardness of 10 gpg.
For water of 20-gpg hardness, scale deposit values can be
multiplied by two. Although the rate of scale deposit is higher
as the temperature increases, significant scale buildup occurs
with cold water. Thus, the cold water scale, while taking a
longer period to build up, is nevertheless significant.
Water Softener Selection
The factors the designer should consider in sizing water
softeners include the following: flow rate, softener capacity, Figure 10-11 Gravel Upheaval
JULY 2013 Read, Learn, Earn 11
READ, LEARN, EARN: Water Treatment
The softener system also should be capable of provid-
ing the design flow rates within the desired pressure drop.
This means not only that the pipe and valve sizes must be
adequate, but also that the water softener tank and its min-
eral must be capable of handling the flows while providing
the soft water. The water softener design should be based on
hydraulic and chemical criteria.
Good design practices for general use dictate that service
flow rates through the water softener be approximately 1–5
gpm per cubic foot with mineral bed depths of 30 inches or
more. Based on these accepted practices, the water softener
is generally able to handle peak flows for short periods.
Standard softener units are designed for a pressure differ-
ential of approximately 15 psi, the most common differential
acceptable for building design. Thus, for general usage, a wa-
ter softener may be selected from a manufacturer’s catalog.
The engineer should give more detailed consideration to the
selection of a water softener where especially low pressure
Figure 10-12 Leaf Design, Diatomaceous Earth Filter
losses are needed. Many equipment manufacturers offer
complete pressure drop curves for their equipment, allow-
listed, the building has one air-conditioner with 5-gpm
ing the selection of components to fit any flow pressure drop
makeup. (Refer to the local code for the specific water
conditions desired.
supply load values used in the area.)
Fixture Count Flow Rate Estimating Guide for
Water Softeners Unit Total
This guide is for estimating average and maximum flow rate Fixtures Weight Weight
requirements (in gallons per minute) for both private and
10 kitchen sinks × 2 = 20
public buildings and is based on fixture flow rates and prob-
ability of use. It is to be used when actual continuous and 10 bathtub/showers × 2 = 20
peak flow rates are not known. 10 lavatories × 1 = 10
The average rates may be used when line pressure less 10 tank-type toilets × 3 = 30
the conditioner pressure drop is at least 30 psi at the highest 3 washing machines × 2 = 6
point of use in the building. The maximum rates are equal to Total = 86
the fixture count figures commonly used to size water lines
For a total of 86 fixture units, the corresponding flow rate
and are applicable especially in low water pressure areas is 31 gpm. Add 31 gpm to 5 gpm for the air-conditioner:
where pressure drop is critical. 31 + 5 = 36 gpm. Select the smallest unit that has a
1. Count and list each type of fixture used intermittently. continuous flow rate of 36 gpm.
Multiply the total of each type by its private or public 4. Select the smallest water conditioner with a continuous
unit weight. Private or public unit weights must be flow rate that is equal to or greater than the total flow
determined by the use of the fixture. For example, lava- rate requirement in step 3.
tories in an apartment house are private. Lavatories in
a restaurant are public. Add the products of each type The line pressure less the pressure drop of the selected
of fixture to determine the total fixture count weight. unit must be at least 30 psi to handle the peak flow rate
periods. If it is less than 30 psi, repeat step 2 using the
2. From the intermittent flow rate chart, select the total maximum column on the intermittent flow rate chart and
fixture count, or the next highest fixture count, deter- add the additional requirements of step 3. Select a water
mined in step 1. conditioner with a continuous flow rate that is equal to
3. Add to the flow rate determined in step 2 any con- or greater than the new total flow rate requirement.
tinuously used flow rates in gallons per minute. These When the maximum figures are used, the line pressure
additional requirements may include commercial dish- less the conditioner pressure drop must be 20 psi mini-
washers, garbage disposals that run continually, boiler mum
makeup water, or swimming pool makeup water. In some
cases, these additional requirements are seasonal and Note: When water conditioners are installed in series,
used separately. For example, if boilers are shut down such as an iron filter in a water softener, the 30-psi and
during the summer, use the additional requirement of 20-psi minimum pressures must be maintained after both
the boiler or the air-conditioning system, whichever is units. Select combinations of conditioners with a total
greater. pressure drop, when subtracted from the line pressure,
Example 10-1 of 30 psi minimum when using the average figures or 20
For example, the flow rate for a 10-unit apartment build- psi when using the maximum figures.
ing can be estimated as follows. In addition to the fixtures
date
Project name
Location
Type of facility
What is water being used for?
Space limitation L W H
Figure 10-17 Water Softener Survey Data
JULY 2013 Read, Learn, Earn 17
READ, LEARN, EARN: Water Treatment
Date
Project name
Location
Step I. Operating conditions
A. Operating hours per day
B. Can regeneration take place once each day? Yes No
C. If “B” is No, state days between regenerations
D. Is a twin unit required? Yes No
E. Type of operation:
Time clock Alarm meter Auto reset meter
F. Allowable pressure loss psi.
Step 2. Flow rate (gpm) (peak, average, continuous)
Step 3. Water usage per day:
× =
Gal/day water usage Water hardness (gr/gal) Required exchange capacity (gr/day)
÷ =
Required exch. cap (gr/day) Resin cap (gr/ft3) Required resin (ft3/day)
Note: If more than one day between regenerations is required, use step no. 7 instead of step no. 6.
Step 7. More than one day of operation per regeneration (step no. 1-B)
Cubic feet of resin required:
× ÷ =
Required exch. cap. (gr/day) Number of days/regn. Resin cap. (gr/ft3) Resin required (ft3)
× =
Required resin (ft3 /regn.) Salt dosage (lb/ft3) Salt regeneration (lb)
Step 9. System selection:
(If auto-reset operation is desired, refer to step no. 10.)
A. Select from the manufacturer’s specification table, a single unit that meets the flow rate (step no. 2).
B. Check that selected unit meets the allowable pressure loss at the flow rate (step no. 1-F).
C. If a single unit will not meet both steps no. 9-A and 9-B, then a multiple unit is required (refer to step no. 10).
D. Check that selected unit contains the required cubic feet of resin (step no. 6 or 7).
E. If single unit will not meet step no. 9-D, then a multiple unit is required. (refer to step no. 10).
F. Select a standard system that meets, or exceeds by no more than 10%, step nos. 9-A, 9-B, and 9-D. If a good balance
is not available, refer to step no. 10.
G. Check that brine-tank salt storage is sufficient to provide a minimum of two regenerations before requiring refill (step
no. 8).
Step 10. Multiple systems:
The following procedure should be followed for a twin unit.
A. Select either auto-reset meter initiation or time clock to start regeneration. Refer to the appropriate subtitle.
Auto-reset meter-initiated regeneration.
B. Select, from the specification table, a tank size that meets the flow rate (step no. 2) and the allowable pressure loss (step
no. 1-F). Each tank in the system must meet these conditions.
C. Divide the required cu. ft. of resin (step no. 6 or 7) by two to determine the required cubic feet of resin contained in the tanks
selected in step no. 10-B. Select a tank large enough to match the required cu. ft. resin/tank.
D. Check that the brine tank salt storage is sufficient to provide a minimum of four regenerations per tank.
Time clock regeneration
E. Divide the flow rate (step no. 2) by 2 to determine the flow rate per tank. Select a tank size that meets this flow rate. (Both
tanks will be on line during the operating period.)
F. Check that the tank selected meets the allowable pressure loss (step no. 1-F) at the flow rate per tank.
G. Follow step no. 10-C to determine the required cubic feet of resin per tank.
H. Follow step no. 10-D to determine the brine tank to be used.
Step 11. Using this data, select a standard system from the softener specifications that most closely matches all the data. If none is
available, a detailed specification should be developed which will allow the manufacturer to match the system requirements.
Step 12. Select options such as ASME code tanks, lining, and materials of construction, as required.
Reverse osmosis is used primarily in industrial applications completely shuts off water flow when the storage tank is full
and in some hospitals and laboratories for specific tasks. It also but allows an hourly washing of the membrane is essential.
is used by some municipalities and end users for the removal Three types of semipermeable membranes are manu-
of dissolved components or salts. factured from organic substances: tubular membrane,
Several types of reverse osmosis units are available. Basi- cellulose-acetate sheet membrane, and polyamide-hollow
cally, they consist of a semipermeable membrane, and water fiber membrane. They may be used for similar applications,
is forced through the membrane under high pressure. A drain assuming that the proper pretreatment for each is furnished.
and storage tank are required with this system. In properly designed and maintained systems, RO mem-
RO is a relatively simple concept. When equal volumes of branes may last two or three years.
water are separated by a semipermeable membrane, osmosis
RO Membranes
occurs as pure water permeates the membrane to dilute the
The current technology of RO developed rapidly as one
more concentrated solution (see Figure 10-24). The amount of
specific application of the larger technology of synthetic
physical pressure required to equalize the two volumes after
membranes. Several code requirements had to be met before
equilibrium has been reached is called the osmotic pressure.
these membranes could be considered practical or economical
If physical pressure is applied in excess of the osmotic pressure,
for water purification processes.
reverse osmosis (see Figure 10-25) occurs as water passes
First, the membrane had to be selective—that is, it had to
back through the membrane, leaving contaminants such as
be capable of rejecting contaminants and yet still be highly
dissolved salts, organics, and colloidal solids concentrated
permeable to water. This condition meant that it had to have
upstream. In practice, the concentrate is diverted to drain,
a consistent polymeric structure with a pore size in the range
thus rejecting contaminants from the system altogether. The
of the smallest contaminant molecules possible.
continuous flushing process of the membrane prevents a
Second, the membrane had to be capable of sustained
phenomenon known as concentration polarization, which is a
high flux rates to be economical and practical in water ap-
buildup of the polarized molecules on the membrane surface
plications. This condition meant that the membrane had to
that further restricts flow in a short period.
be thin and yet durable enough for long-term use.
For dependable long-term performance, RO equipment for
Developments in membrane technology led to a membrane
large-volume applications should be of all stainless steel fit-
with a thin skin (approximately 0.05 µ) cast on top of a po-
tings and bowls. Such a system should use solid-state controls
rous support structure (100 µ thick). This resulted in high
(with simple indicator lights and gauges) plus a conductivity
flux rates, selectivity, and structural strength. The resulting
meter that reads the tap and permeates water quality. High-
RO membrane proved to be highly resistant to chemical and
pressure relief devices and low-pressure switches protect
microbial degradation. It also could maintain the required
the membrane and the pump from any prefilter blockage
water quality and flow rates under a sustained high pressure.
and accidental feed water shutoff. A water-saver device that
Such a membrane could be incorporated into a system with
relatively low capital, equipment, and operating costs. These by exchanging them with sodium salts). The reverse osmosis,
attributes were combined successfully, and the resulting deionization, and distillation processes are all capable of
membrane achieved a flow rate of 20 gallons per square foot producing laboratory-grade water.
per day at 800 psi with 95 percent removal of salt. The quality of the laboratory-grade water produced by
several methods of central-system water production is shown
RO Water Quality
in Table 10-4. The RO and distillation processes remove more
The term high purity often is applied to a type of water that
than 99 percent of all bacteria, pyrogens, colloidal matter,
may be exceptionally free of one class of contaminant and yet
and organics above molecular weight 200. These methods
may contain large amounts of another. The key, of course, is
remove the dissolved inorganic material, such as multivalent
the application involved. One useful distinction is between
ions, calcium, magnesium, carbonates, and heavy metals to
reagent-grade water and laboratory-grade water. Reagent-
the level of 98 percent, while monovalent ions, such as so-
grade water means that all classes of contaminants have been
dium, potassium, and chloride, are removed to the level of 90
removed from the water. Several nationally recognized stan-
percent to 94 percent by RO and 97 percent by distillation.
dards for reagent-grade water are published by ASTM and
Large-scale deionization processes achieve similar levels
the College of American Pathologists (CAP). The minimum
of inorganic ion removal, but they do not remove bacteria,
resistivity for reagent-grade water is 10 MΩ-cm at 25°C. The
production of reagent-grade water always
requires more than one stage of treatment. Table 10-4 Comparison of Laboratory-Grade Water Quality Produced by
It should be produced at the point of use Centralized Systems
to minimize (or eliminate) transportation Reverse Osmosis Distilled Deionized
and storage, which invariably degrade Tap, Percent Percent Percent
the reagent water purity. A system for Contaminant Typical Actual Removal Actual Removal Actual Removal
producing reagent-grade water might, for Microorganism/ mL 100 1 >99 1 >99 1000 a none
example, use the RO process to produce Particles 5 µm/mL 10,000 1 >99 200 >97 10,000 none
laboratory-grade water, plus a combina- Pyrogens Variable — >99 — >99 Variable none
tion of activated carbon, deionization, Dissolved
organics ppm 12 1 >95 1 >95 12 b none
and 0.20-µ membrane filtration. Only the
Dissolved
laboratory-grade water would be accumu-
inorganics ppm CaCO3 170 1–17 >90–98 1–8 >95–99 1–8 >95–99
lated and stored. The reagent water would Monovalent ions c — — >90 — >97 — >97
be produced at high flow rates as needed, Multivalent ions d — — >97 — >97 — >97
thus eliminating the need to store it. Conductivity, µS, 25°C 333 2–40 — 2–10 — 2–10 —
Laboratory-grade water is less rigor- Specific resistance
0.003 0.025–0.5 — 0.1–0.5 — 0.1–0.5 —
ously defined, but it still refers to water MΩ/cm, 25°C
from which one or more types of contami- Silicates ppm 1 0.1 >90 0.1 >90 0.1 >90
nants have been removed. This definition Heavy metals ppm 1 0.1 >97 0.1 >97 0.1 >90
should be distinguished from other pro- pH 7.5 6. 8 — 4–7. 5 — 7.0 —
cesses that exchange one contaminant for a
Bacteria often multiply in large deionizing (D.I.) resin beds used directly on tap water.
another, such as water softening (in which c Large D.I. resin beds also contribute organics from+ the+ resin– beds.
b
Figure 10-26 Approaches to Providing Laboratory-Grade and Reagent-Grade Water: (A) RO Water
Purified Centrally and Transported by Pipe to Points of Use Then Polished, (B) RO System Coupled with
Deionization System Totally at the Point of Use, Eliminating Piping