Problems Caused by Iron and Manganese in Household Water
Neither iron nor manganese in water present a health hazard. However, their presence in
water may cause taste, staining, and accumulation problems.
Because iron and managanese are chemically similar, they cause similar problems. Iron
will cause reddish-brown staining of laundry, porcelain, dishes, utensils, and even
glassware. Manganese acts in a similar way but causes a brownish-black stain. Soaps and
detergents do not remove these stains, and the use of chlorine bleach and alkaline
builders (such as sodium carbonate) can actually intensify the stains.
Iron and manganese deposits will build up in pipelines, pressure tanks, water heaters,
and water softeners. This reduces the available quantity and pressure of the water supply.
Iron and manganese accumulations become an economic problem when water supply or softening
equipment must be replaced. There are also associated increased energy costs, like pumping
water through constricted pipes or heating water with heating rods coated with iron or
manganese minerals.
Sources of Iron and Manganese in Household Water
Iron and manganese are concentrated in water by contact with rocks and minerals, and
occasionally man-made materials like iron and steel pipes. It is usually groundwater
supplies that may require treatment for high levels of iron and manganese. Generally
speaking, few surface water supplies have high enough levels of either to cause problems.
Occasionally discharge of acid industrial wastes or mine drainage may increase iron or
manganese to problem levels in surface water.
Iron and Manganese Solubility
Iron and manganese exist in many different chemical forms. The presence of a given form
of iron or manganese in geologic materials or water depends on many different
environmental factors. We can often anticipate iron and manganese problems in water by
observing a few general principles that affect water chemistry.
An important principle to remember about chemical reactions is that, if allowed enough
time, they will reach an equilibrium with the surrounding environment. When the conditions
of that environment are changed, such as pumping water from an underground acquifer, the
chemical equilibrium is upset. This will lead to either solution of certain elements such
as iron and manganese or their precipitation.
A general rule of thumb is that oxygenated water will have only low levels of iron and
manganese. The reason is that both iron and manganese react with oxygen to form compounds
that do not stay dissolved in water. Surface water and shallow groundwater (Figure 1)
usually have enough dissolved oxygen to maintain iron and manganese in an undissolved
state. In surface water, iron and manganese are most likely to be trapped within suspended
organic matter particles.
Waters that do not have regular contact with the atmosphere tend to be low in oxygen
(oxygen poor). Iron and manganese carbonates in an oxygen poor environment are relatively
soluble and can cause high levels of dissolved iron and manganese. However, if iron is
associated with sulfur as iron sulfide rather than iron carbonate, dissolved iron remains
low. Dissolved oxygen generally decreases with depth, so these types of conditions are
more likely to occur in deep wells. Sometimes oxygen poor conditions can also occur in
relatively shallow wells that have stagnant water with very slow turnover.
Iron and manganese problems are most likely to develop in water from wells with high
carbonate and low oxygen as shown in the middle well in Figure 1. Problems occur when this
type of water is pumped to the surface. The chemical equilibrium is changed upon exposure
to the atmosphere. The end result is precipitation of iron and manganese compounds in
plumbing, on fixtures, and on clothing, dishes, and utensils.

Figure 1. The amount of iron and manganese
dissolved in water often follows a trend of low to high back to low again as depth of the
well increases. (Snoeyink, V. L. and D. Jenkins, 1980)
Iron and Manganese Bacteria
Some types of bacteria derive their energy by reacting with soluble forms of iron and
manganese. These organisms are usually found in waters that have high levels of iron and
manganese in solution. The reaction changes the iron and manganese from a soluble form
into a less soluble form, thus causing precipitation and accumulation of black or reddish
brown gelatinous material (slime). Masses of mucous, iron, and/or manganese can clog
plumbing and water treatment equipment. They also slough off in globs that become iron or
manganese stains on laundry. Bacterial reactions with iron and manganese do not cause any
additional precipitation compared to normal exposure to oxygen. However, precipitation
caused by bacteria occurs faster and tends to concentrate staining, thus making it more
apparent.
Water System Pipelines
An additional source for dissolved iron may be the pipelines through which water flows.
Water with high salinity or acidity from dissolved carbon dioxide or other acids will be
corrosive to metal pipes. In order to establish equilibrium, iron and other metals will be
dissolved from the pipelines. If household pipes are being attacked by corrosive water and
cause problem levels of metals such as iron, copper, and lead, the water can be treated to
reduce corrosivity and level of dissolved metals.
Acidity can be reduced by either adding alkaline materials such as sodium carbonate or
passing water through filters made of alkaline material. Salinity can be treated by either
distillation or reverse osmosis.
Because different metals are more or less corodable, a solution to the problem may be
to use a more resistant metal. A plumber should be consulted regarding materials that are
best suited to local water conditions.
How Much Is Too Much?
How much iron or manganese in the water is needed to cause these sorts of problems?
There is no pat answer to this question, because it varies with each household situation.
Standards for iron and manganese are based on levels that cause taste and staining
problems and are set under EPA Secondary Drinking Water Standards. For most individuals
0.3 parts per million (ppm) of iron and 0.05 ppm of manganese is objectionable. Usually
iron and manganese do not exceed 10 ppm and 2 ppm, respectively, in natural waters. Iron
and manganese are found at higher concentrations; however, that condition is rare.
Water Treatment for Iron and Manganese Removal
Polyphosphate Treatment
Polyphosphates react with dissolved iron and manganese by trapping them in a complex
molecule that is soluble in water (Figure 2). As a result the iron and manganese are not
available to react with oxygen and precipitate. Polyphosphates can be fed into the water
system with controlled injection equipment. Polyphosphates are not stable at high
temperatures. If water is treated prior to heating in a water heater, the polyphosphates
will release iron and manganese in the heater as they break down. The released iron and
manganese will then react with oxygen and precipitate.
Polyphosphate treatment is a relatively cheap way to treat water for low levels of iron
and manganese. Depending on the type of polyphosphate used, water with 1 to 3 ppm of iron
can be adequately treated.

Figure 2. Polyphosphates protect dissolved
iron and manganese from reacting with oxygen and precipitating on household appliances,
bath/plumbing fixtures, and laundry.
Ion Exchange
Soluble iron and manganese (iron and manganese dissolved in water) can be exchanged for
sodium on an exchange resin or zeolite (Figure 3). This process of iron and manganese
removal is the very same ion exchange process that removes hardness or calcium and
magnesium (refer to the softening circular in the Treatment Systems for Household Water
Supplies series). Iron and manganese are removed during normal operation of the water
softener. They are later removed from the exchange medium along with calcium and magnesium
during regeneration and backwashing. Some water softeners are capable of adequately
treating water having iron up to 10 ppm. However, others are limited to treating water
with iron no greater than 1 ppm. If iron and manganese removal is desired in addition to
hardness, the manufacturer's recommendations should be checked.

Figure 3. Household water softening units will
remove some iron and manganese from water. Most units, however, are not designed to handle
very large amounts of iron and manganese and may become plugged when concentrations are
high.
One of the disadvantages of depending on ion exchange for iron and manganese removal is
precipitation by oxygen. Some of the precipitate becomes tightly bound to the exchange
resin and over time reduces the exchange capacity by plugging pores and blocking exchange
sites. If iron bacteria are present, the problem is even worse. Also, if suspended
particles of insoluble forms of iron or manganese are present in the water prior to
softening, they will be filtered out on the resin and cause plugging. Suspended iron and
manganese should be filtered out before water enters the softener.
A clogged water softener can be cleaned by acid regeneration if the unit is made to
withstand acid corrosion. The manufacturer should be consulted before this is attempted.
The problem with iron bacteria can be eliminated by chlorinating (Refer to the
Chlorination circular in the Treatment Systems for Household Water Supplies series) and
filtering the water at some point before it reaches the softener. As long as levels of
iron and manganese in the water do not exceed the manufacturer's recommendations, iron and
manganese clogging should not be a significant problem. When iron and manganese levels are
higher than recommended by the manufacturer, iron and manganese removal will be necessary
prior to softening.
Greensand (Adsorptive/Oxidative) Filtration
One of the first types of filters to be used to treat water was the
"greensand" filter. The active material in "greensand" is glauconite.
Glauconite is a green clay mineral that contains iron and has ion exchange properties.
Glauconite often occurs mixed with other material as small pellets, thus the name
"greensand." The glauconite is mined, washed, screened, and treated with various
chemicals to produce a durable greenish-black product that has properties that allow it to
adsorb soluble iron and manganese.
As water is passed through the filter, soluble iron and manganese are pulled from
solution and later react to form insoluble iron and manganese. Insoluble iron and
manganese will build up in the greensand filter and must be removed by backwashing.
Backwashing should be done regularly twice a week or as recommended by the manufacturer.
Eventually the greensand must also be regenerated by washing with a permanganate
solution. Regeneration will leave the greensand grains coated once again with a manganese
material that adsorbs soluble iron and manganese. Frequency of regeneration will depend on
the level of iron, manganese, and oxygen in the water and the size of the filter. The
manufacturer's recommendations should be followed.
Most greensand filters are rated to be effective treating water with iron
concentrations up to 10 ppm. Because some greensand filters are not rated this high, the
manufacturer's recommendations should always be checked. The acidity or pH of the water
will influence the ability of the filter to remove both iron and manganese. If the pH of
the water is lower than 6.8, the greensand will probably not adequately filter out the
iron and manganese. The pH can be raised above 7.0 by running the water through a calcite
filter.
Regular backwashing is essential for effective filter performance and require flow
rates that are often three to four times the normal household useage rate. A backwash rate
of about eight gpm/square foot of filter bed is recommended. If the household system
cannot support the needed flowrate for adequate backwashing, poor filter performance and
failure are likely.
Chlorination (Oxidation) Plus Filtration
Chemical oxidation followed by filtration is the accepted method of iron and manganese
removal when concentrations are greater than 10 ppm. There are a number of strong oxidants
that have been used in this procedure; however, chlorine is generally used in household
systems (Refer to the Chlorination circular in the Treatment Systems for Household Water
Supplies series).
A chlorine solution is injected with a chemical feed pump ahead of a sand filter.
Soluble iron and managanese begin to precipitate almost immediately after contact with the
chlorine solution. However, approximately 20 minutes of contact time is needed for the
precipitate to form particles that can be filtered. Often the standard 42 gallon pressure
tank used on many household systems will provide the needed contact time if water is
forced through the tank. A simple T-connection from the pipeline to the pressure tank will
not work, since much of the water bypasses the tank. Additional contact time can be
provided by connecting another tank in series or using a plastic pipe coil.
This type of system will remove both soluble and suspended particles of insoluble iron
and manganese from the source water. Backwashing the sand filter to remove precipitated
iron and manganese is an important part of continued filtration. As with the
"greensand" filter, the system flow rate should be checked to make sure it can
provide the needed rates for backwashing.
An additional advantage of using the chlorination system is its bacteriacidal effect.
Iron and manganese bacteria, along with other bacteria, are destroyed. Potential clogging
problems in the sand filter are eliminated. Chlorination does produce trihalomethanes
(THM) when organic matter is present in the water. THMs are considered to be carcinogenic
(maximum contaminant level permissible in public water systems is 0.1 parts per million)
and if necessary can be filtered out with an activated charcoal filter (refer to the
activated charcoal filtration circular in the Treatment Systems for Household Water
Supplies series).
The optimum rate of oxidation of iron and manganese by chlorination is at a pH of about
8.0 and 8.5, respectively. Soda ash injected with the chlorine will increase the pH to
optimum levels. Adjusting the pH to alkaline levels also reduces the corrosivity of the
water to pipes and plumbing.
Standards for Iron and Manganese Removal Equipment
The Water Quality Association (WQA) has set voluntary performance standards for
oxidative filtration methods. "An oxidizing filter shall reduce 10.0 ppm plus or
minus 1.0 ppm soluble iron to not more than 0.2 ppm and 2.0 ppm plus or minus 0.2 ppm
soluble manganese to not more than 0.05 ppm." A directory of validated equipment that
meet these standards is available from WQA, National Headquarters and Laboratory, 4151
Naperville Road, Lisle, IL 60532 (708/505-0160).
WQA also recognizes that the following water treatment methods can be used to meet
EPA's Secondary Drinking Water Standards for both soluble iron and manganese: 1) oxidizing
filters; 2) cation exchange; and 3) chlorination - precipitation/filtration. Polyphosphate
treatment does not meet the drinking water standards, because it ties up iron and
manganese but does not remove it. Reverse osmosis, distillation, (Refer to the Reverse
Osmosis and Distillation circulars in the Treatment Systems for Household Water Supplies
series) and pressure aeration/filtration are also recognized by WQA as water treatment
methods that can be used to meet the iron and manganese drinking water standards.
The consumer should be cautioned to note that different water treatment systems vary
considerably in their ability to treat a specific contaminant. Water treatment equipment
should be selected only after careful consideration of the water problem and type of
equipment to be used for its removal. As a part of the installation procedure, the
performance of the equipment should be tested by water analysis. Periodic water analysis
is recommended to check for continued equipment performance.
Hem, J. D. 1967. Equilibrium chemistry of iron in groundwater. In S. D. Faust and J. V.
Hunter (ed.) pp. 625-643, Principles and applications of water chemistry. John Wiley and
Sons, Inc., New York.
Machmeier, R. E. Reviewed 1990. Iron in drinking water, AG-FO-1318. Minnesota Extension
Service, University of Minnesota, Agriculture.
O'Connor, J. T. 1971. Iron and Manganese. In M. E. Flentje and R. J. Faust (ed.) pp.
380-396, Water quality and treatment - a handbook of public water supplies, 3rd Edition.
Prepared by The American Water Works Association, Inc. McGraw-Hill Book Co., New York.
Snoeyink, V. L. and D. Jenkins. 1980. Water Chemistry. John Wiley and Sons, Inc., New
York.
Water Quality Association. 1988. Recommended industry standards for household and
commercial water filters - a voluntary industry standard, S-200. National Headquarters and
Laboratory, Lisle, Illinois.
Water Quality Association. 1989. Recognized treatment techniques for meeting the
national secondary drinking water regulations with the application of point-of-use
systems, R28. National Headquarters and Laboratory, Lisle, Illinois.