Basic Ion Exchange Processes
Basic Ion Exchange Processes
You will find here a description of the above processes, the exchange reactions and the changes in water.
Resin types are described in another page, as well as regeneration methods. See also the general
introduction to ion exchange, and an overview of ion exchange column designs in other pages.
Softening
Natural water contains calcium and magnesium ions (see water analysis) which form salts that are not very
soluble. These cations, together with the less common and even less soluble strontium and barium cations,
are called together hardness ions. When the water evaporates even a little, these cations precipitate. This is
what you see when you let water evaporate in a boiling kettle on the kitchen stove.
Hard water also forms scale in water pipes and in boilers, both domestic and industrial. It may create
cloudiness in beer and soft drinks. Calcium salts deposit on the glasses in your dishwasher if the city water is
hard and you have forgotten to add salt.
Strongly acidic cation exchange resins (SAC, see resin types) used in the sodium form remove these hardness
cations from water. Softening units, when loaded with these cations, are then regenerated with sodium
chloride (NaCl, table salt).
Reactions
R represents the resin, which is initially in the sodium form. The reaction for magnesium is identical.
The above reaction is an equilibrium. It can be reversed by increasing the sodium concentration on the right
side. This is done with NaCl, and the regeneration reaction is:
SAC (Na)
The water salinity is unchanged, only the hardness has been replaced by sodium. A small residual hardness is
still there, its value depending on regeneration conditions.
Uses
Softening the water does not reduce its salinity: it merely removes the hardness ions and replaces them with
sodium, the salts of which have a much higher solubility, so they don't form scale or deposits.
De‐alkalisation
This particular process uses a weakly acidic cation resin. This resin type is capable of removing hardness from
water when it also contains alkalinity. After treatment, the water contains carbon dioxide, that can be
eliminated with a degasifier tower. The cation resin is very efficiently regenerated with an acid, usually
hydrochloric acid.
Reactions
and the hydrogen cations combine with the birarbonate anions to produce carbon dioxide and water:
H + + HCO3– CO2 + H 2O
WAC (H)
DEG
Uses
De‐alkalisation is used:
In breweries
In household drinking water filters
For low pressure boilers
As a first step before the SAC exchange in demineralisation
De‐alkalisation reduces the salinity of water, by removing hardness cations and bicarbonate anions.
Decationisation
The removal of all cations is seldom practiced, except as a first stage of the demineralisation process, or
sometimes in condensate polishing where the decationiser precedes a mixed bed unit. A strongly acidic
cation exchange resin (SAC) is used in the H+ form.
Reactions
Here the example of sodium, but all cations react in the same way:
The equilibrium reaction is reversed for regeneration by increasing the hydrogen concentration on the right
side. This is done with a strong acid, HCl or H2SO4:
In the second step, a degasifier is used again to remove the carbon dioxide formed by combining the
bicarbonate anions and the released hydrogen cation. The water salinity is reduced, and the water is now
acidic. A small sodium leakage is shown.
Demineralisation
For many applications, all ions in the water must be removed. In particular, when water is heated to produce
steam, any impurity can precipitate and cause damage. As there are cations and anions in the water, we must
use two different types of resins: a cation exchanger and an anion exchanger. This combined arrangement
produces pure water, as presented in the general introduction. Demineralisation is also called deionisation.
The cation resin is used in the hydrogen form (H+) and the anion resin in the hydroxyl form (OH–), so that the
cation resin must be regenerated with an acid and the anion resin with an alkali.
A degasifier is used to remove the carbon dioxide created after cation exchange when the water contains a
significant concentration of bicarbonate.
The cation resin is usually located before the anion resin: otherwise if the water contains any hardness, it
would precipitate in the alkaline environment created by the OH— form anion resin as Ca(OH)2 or CaCO3,
which have low solubility.
Let us first consider a simple demineralisation system comprising a strong acid cation exchange resin in the
H+ form, a degasifier (optional) and a strong base anion exchange resin in the OH– form. The first step is
decationisation as shown above:
With calcium insead of sodium (also valid for magnesium and other divalent cations):
In the second step, all anions are removed with the strong base resin:
The weak acids created after cation exchange, which are carbonic acid and silicic acid (H2CO3 and H2SiO3) are
removed in the same way:
And finally, the H+ ions created in the first step react with the OH– ions of the second step to produce new
molecules of water. This reaction is irreversible:
H + + OH – H 2O
Demineralised water is completely free of ions, except a few residual traces of sodium and silica, because
the SAC and SBA resins have their lowest selectivity for these. With a simple demineralisation line
regenerated in reverse flow, the treated water has a conductivity of only about 1 µS/cm, and a silica residual
between 5 and 50 µg/L depending on the silica concentration in the feed and on regeneration conditions.
Note that the pH value should not be used as a process control, as it is impossible to measure the pH of a
water with less than say 5 µS/cm conductivity.
Regeneration
And the SBA resin is regenerated with a strong alkali, NaOH in 99 % of the cases:
Because weakly acidic and weakly basic resins offer a high operating capacity and are very easy to
regenerate, they are used in combination with strongly acidic and strongly basic resins in large plants. The
first step with the WAC resin is dealkalisation (removal of bicarbonate hardness), and the second step with
the SAC removes all the remaining cations. A WAC resin is used when both hardness and alkalinity are present
in large relative concentrations in the feed water.
WBA resins remove only the strong acids after cation exchange. They are not capable of removing the weak
acids such as SiO2 and CO2. In the regenerated, free base form, they are not dissociated, so no free OH– ions
are available for neutral anion exchange. On the other hand, their basicity is enough to adsorb the strong
acids created after cation exchange:
In the last step, a SBA resin is thus required to remove the weak acids, as shown in the preceding section:
1 & 2: Cation exchange beginning with the removal of temporary hardness (WAC, as in dealkalisation)
followed by the removal of all remaining cations (SAC):
Regeneration
Regeneration is done in thoroughfare, which means that the regenerant first goes through the strong resin,
which requires an excess of regenerant, and the regenerant not consumed by the strong resin is usually
sufficient to regenerate the weak resin without additional dosage.
The cation resins are regenerated with a strong acid, preferably HCl, because H2SO4 can precipitate calcium.
The anion resins are regenerated with caustic soda.
The quality obtained is the same as in the simple SAC‐SBA layout, but because the weak resins are
practicallly regenerated "free of charge", the regenerant consumption is considerably lower. Additionally, the
weak resins have a higher operating capacity than the strong resins, so the total volume of ion exchange
resins is reduced.
Uses
Examples of demineralisation:
Water for high pressure boilers in nuclear and fossil fuelled power stations and other industries
Rinse water used in production of computer chips and other electronic devices
Process water for many applications in the chemical, textile and paper industries
Water for batteries
Water for laboratories
Mixed bed units deliver an excellent treated water quality, but are
complcated to regenerate, as the resins must first be separated by
backwashing before regeneration. Additionally, they require large
amounts of chemicals, and the hydraulic conditions for regeneration
are not optimal. Therefore, mixed beds are usually only used to treat
pre‐demineralised water, when the service run is long.
Mixed bed polishing produces a water with less than 0.1 µS/cm conductivity. With sophisticated design and
appropriate resins, the conductivity of pure water (0.055 µS/cm) can be achieved. Residual silica values can
be as low as 1 µg/L.
The pH value should not be used as a process control, as pH meters are unable to operate at 1 µS/cm
conductivity or below.
Uses
Nitrate removal
Nitrate can be removed selectively from drinking water using strong base anion resins in the chloride cycle,
i.e. regenerated with a NaCl brine. The reaction is:
SBA (Cl)
Conventional SBA resins can be used, but they also remove sulphate from water. See the selectivity table.
Depending on the resin type, some (selective resins) or all (non‐selective) sulphate is removed. Bicarbonate
is only removed partially at the beginning of the service run.
Uses
Examples
Some contaminants are difficult to remove with ion exchange, due to a poor selectivity of the resins.
Examples: As, F, Li. See the periodic system of the elements with some ion exchange data. See also the page
about resin types (selective resins) and a separate page about ion exchange processes for drinking water.
Other information
Abbreviations
Resin types are usually abbreviated in these pages:
Water
See details about the water analysis as required for the above processes.
A special page is available about drinking water applications.
Regeneration
See details about regeneration processes, quantities and concentrations of regenerants.
© François de Dardel