EDTA Titration For Determination of Calcium and Magnesium: Chemistry 321: Quantitative Analysis Lab Webnote 7

Chemistry 321: Quantitative Analysis Lab Webnote 7
EDTA Titration for Determination of

Calcium and Magnesium
Before attempting this experiment, you may need to consult the section in the textbook dealing
with complexometric titrations. In this procedure a stock solution of EDTA will be standardized
against primary standard CaCO3. This standardized EDTA solution is then used to determine
water "hardness" – the total calcium and magnesium content, typically expressed as equivalent
calcium carbonate mass concentration. While both metals are nutrients that are needed for
good human health, high concentrations of these cations (Ca2+ and Mg2+) in water can cause
deposits to form in bathrooms and kitchens, and cause the formation of “soap scum” – clogging
pipes and decreasing the effectiveness of the cleanser. Therefore, very hard water is
undesirable for use as tap water. Guidelines for classification of water as provided by the U.S.
Geologic Survey are listed in the table below. The USGS website has more information about
water hardness and alkalinity if you are interested. We're fortunate in that most of the water in
the Portland area is soft.
Table 1 U.S. Geological Survey Classification of Water Hardness
(Source: http://water.usgs.gov/owq/hardness-alkalinity.html)
CaCO3 (mg/L) Hardness
0-60 soft
61-120 moderately hard
121-180 hard
>180 very hard
Figure 1 Hardness classification from Briggs et al. 1977

Briggs, J.C., and Ficke, J.F., 1977, Quality of Rivers of the United States, 1975 Water Year -- Based on the
National Stream Quality Accounting Network (NASQAN): U.S. Geological Survey Open-File Report 78-200,
436 p.
A complex is a molecule or ion formed from the reaction of two or more individually stable ions
or molecules, but the reaction is driven by the electron deficiency of metal ions. The most
important complexation reactions from an analytical point of view are those between a metal
ion in solution and a complexing agent known as a ligand or chelate. The metal ions are Lewis
acids and readily share electron pairs with the electron-donating ligands (Lewis bases). As an
example, cyanide (CN-) binds to a metal ion through a lone pair on one atom and is thus a
monodentate (one tooth) ligand. Many transition metal ions will share up to six electron pairs
with ligands. A ligand that bonds to a metal ion using more than one ligand atom is called a
multidentate (many toothed) ligand or a chelate (or sometimes a chelating agent).
In a complexometric titration, a solution containing the free metal ion of interest is titrated
with a solution of a chelating agent until all of the metal ions are bound. The endpoint is usually
signaled by an indicator ligand that forms a colored complex with the free metal ion.
Figure 2 EDTA – a chelate used by industry and analytical chemists
The most important chelating agent in analytical chemistry is ethylenediaminetetraacetic acid

(EDTA). EDTA is a hexadentate ligand (Figure 2) and can exist as a hexaprotic acid H6Y2+
although the neutral form is tetraprotic (all of the pKa values are listed in Figure 3).
Figure 3. Top: structure o EDTA acidic form; bottom: pKa values

(source: D. C. Harris Quantitative Chemical Analysis 8th Ed)
The most basic form of EDTA (Y4-) forms complexes with virtually all metal ions, except the alkali
metals. EDTA always complexes metals with 1:1 stoichiometry.
Unfortunately EDTA cannot be easily used as a primary standard. The H4Y form can be dried at
140◦C for 2 hrs and used as a primary standard, but is only sparingly soluble in water. The
reagent-grade Na2H2Y2▪2H2O contains 0.3% excess water and must be dried at 80◦C for several
days to remove the excess water and obtain the dihydrate. Standardization of EDTA against a
primary standard metal ion (in this case, the one to be determined) is easier and more reliable.
The electron pairs of the carboxylic acid groups of EDTA are only available to the metal ion
when the acid is dissociated, implying that the effectiveness of the complexing agent is
maximized at high pH. Unfortunately many metal ions form complexes or insoluble precipitates
with hydroxide ions, so for a given chelating agent and metal ion, there may be an optimum pH
for the titration. In the case of EDTA titrations of calcium and magnesium there is little chance
of reaction with hydroxide and the effectiveness of the EDTA must be maximized, so the pH is
buffered at a high value, near 10.
Calmagite (3-hydroxy-4-(2-hydroxy-5-methylphenylazo) naphthalene-1-sulfonic acid) earns its

name by serving as the indicator of choice for this titration, but it is necessary to add a small
amount of Mg2+ to obtain a sharp end point. This necessitates a blank titration to separate the
contribution from the added magnesium.
Figure 4. Calmagite structure
In the titration EDTA forms a weaker complex with Mg2+ than Ca2+, so Y4- reacts with Ca2+ first,
leaving the red MgIn- solution
Ca2+ + MgIn- (red) + Y4- CaY2- + MgIn- (red)
When all the Ca2+ is bound by Y4-, MgIn- reacts with Y4- to release the indicator
MgIn- (red) + Y4-  MgY2- + In3- (colorless)
In3- which then hydrolyzes to produce the color change that signals the endpoint of the titration.
In3- (colorless) + H2O  Hln2- (blue) + OH-
Standardization of EDTA
Prepare 0.01 M EDTA solution in 0.16 M Sodium Glycine Buffer: Add approximately 0.88 g of
dry disodium EDTA salt and 25 mL glycine buffer solution to about 100 mL of DI water in a 250
mL beaker and swirl periodically. (Water used in the preparation of standard EDTA solutions
must be totally free of polyvalent cations. The volume of the beaker doesn’t really matter, it is a
container to dissolve the solid.) Dissolution may take 15 min. or longer, so start this part as soon
as possible. If complete dissolution does not occur in 15 min. the solution can be decanted and
used, since it will be standardized in the next step, but the remaining solid must be removed to
prevent additional dissolution.
Test the pH of the solution using universal pH paper. Ideally, pH should be ≥ 10.3 (if not, consult
your TA). Transfer to a 250 mL volumetric flask, dilute to the mark with DI water, and mix well.
Prelab calculation: Calculate the expected molarity of the EDTA solution, correcting the mass of
the Na2H2Y salt for the 0.3% moisture it ordinarily retains after drying.
Primary standard calcium carbonate should have been oven dried for at least two hours at 110
ºC (Note 1). Weigh (to 0.1 mg) about 0.3 grams of calcium carbonate and transfer to a beaker.
Add 25 mL of calcium free DI water, and then slowly add one full Pasteur pipet loading of 6 M
HCl with a dropper until all of the calcium carbonate dissolves (Note 2a). Be careful to avoid loss
of solution due to rapid foaming or splattering as CO2 is evolved. Make certain dissolution is
complete - undissolved solid may stick to the upper wall of the flask and very small particles are
difficult to see. Warm the solution gently (Note 2b). Then cool and transfer quantitatively to
your calibrated 250 mL volumetric flask. Fill to the mark with DI water and mix well. Calculate
the molar concentration of calcium.
Pipet 25.00 mL aliquots of the standard calcium solution into three 250-mL Erlenmeyer flasks.
Right before titrating, add 1.00 mL of 0.001 M magnesium solution (MgCl2) and 4.0 mL
Calmagite indicator solution. (Note 3) Titrate with EDTA until the color changes to a clear blue.
There should be no reddish or purple tint at the end point.
In the above titrations, magnesium was added in order to obtain a sharper color change at the
end point. However, EDTA reacts with magnesium in exactly the same way as it does with
calcium. It is therefore necessary to subtract the volume of EDTA required to titrate the added
magnesium. This is called an indicator blank. Repeat the titration with EDTA exactly as above;
but substitute 25 mL of DI water for the standard calcium solution. This titration will require
very little titrant. Repeat the blank determination three times or more until you are confident
of the volume. You will subtract the mean of the blank volume measurements from all
titrations in which calcium was present. With the results above, you can now calculate the
concentration of your standardized EDTA solution.
Determination of Water Hardness

Measure out 100 mL aliquots of the hard water sample using a volumetric pipet into three 250-
mL Erlenmeyer flasks. To each sample, add the magnesium solution and the Calmagite indicator
as above. (Note 3) Titrate with the standardized EDTA solution. Correct the volume of titrant by
subtracting the indicator blank. Calculate the molar concentration of “calcium” in the hard
water sample.
It is common practice to report water hardness in terms of the number of milligrams of CaCO3
per liter. That is, regardless of the form of the calcium (or whether it even was calcium, since
magnesium would be indistinguishable) we calculate the result as if all of the material that
reacted with EDTA was calcium carbonate. This is a common analytical practice. For example,
you will see the phosphates in fertilizer reported as phosphoric acid.
REQUIRED MEASUREMENTS
At the end of the period, you must present the results for the standardization of the EDTA and
for the calcium content (hardness as mg CaCO3 per liter) of the hard water to your lab TA
before leaving. The results include the mean, standard deviation, and relative standard
deviation (in ppth) of your replicate determinations.
Sample Results Table

Concentration Stdev RSD (‰)
EDTA (M)
Hardness (mg/L)
NOTES
1) Standard operating procedure is to dry for one hour at 110 ºC. However, in a lab with many
students opening and closing the oven, the temperature will drop. Please replace the solid and
close the oven when you are done dispensing and do not use the solid if it has been out of the
oven for more than a minute or two.
2a) Ideally you should add the minimum amount of HCl needed to dissolve the CaCO3. If you
add too much HCl, then the glycine buffer in the EDTA titrant will not work properly – i.e. we
have to keep the pH near the endpoint of the titration at or slightly above 10. This is important
because reactions between metal ions and EDTA are pH dependent - for divalent ions solutions
must be kept basic for the reaction to go to completion.
Buffer range of the glycine/NaOH: 8.6-10.6
Calmagite indicating pH: 8.5-11 for Ba, Ca, Mg, Zn
2b) "Warm" means just that. Not hot, and certainly not boiling! The acidification and heating
step is to remove carbonates; which if present, will precipitate CaCO3 when the solution is
made basic. The precipitate obscures the end point.
3) Always use the same bottle of magnesium solution and Calmagite indicator!
Last update: Oct. 2015

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Chemistry 321: Quantitative Analysis Lab Webnote 7

EDTA Titration for Determination of

Figure 1 Hardness classification from Briggs et al. 1977

Figure 2 EDTA – a chelate used by industry and analytical chemists

The most important chelating agent in analytical chemistry is ethylenediaminetetraacetic acid

Figure 3. Top: structure o EDTA acidic form; bottom: pKa values

Calmagite (3-hydroxy-4-(2-hydroxy-5-methylphenylazo) naphthalene-1-sulfonic acid) earns its

Figure 4. Calmagite structure

Determination of Water Hardness

Sample Results Table

Last update: Oct. 2015

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