Vous êtes sur la page 1sur 1

In the Laboratory

Complexometric Titration of Zinc

An Analytical Chemistry Laboratory Experiment
S. G. Novick
Department of Chemistry, 135 Hofstra University, Hempstead, NY 11549-1350
Complexometric titrations with EDTA have traditionally been performed in undergraduate analytical chemistry
courses to determine the calcium or magnesium content of
water. These titrations are performed at a basic pH, where
the formation constants of Ca-EDTA and Mg-EDTA complexes are high. These types of problems are well-treated
in the analytical chemistry textbooks (1, 2). In contrast,
treatment of metal ions whose EDTA complexes occur significantly at low pH (e.g., Zn2+, Fe3+ , Cu2+, Ni2+, Pb 2+, Al3+)
(3) is sparse. An incorrect conclusion can be reached by the
student that practical EDTA titrations are only performed
at high pH. In addition, widening the window of possible
metal ions for complexometric titration affords the possibility of analyzing real world products, such as the cold
lozenges discussed below.
Zinc content in a sample can be determined quantitatively by complexometric titration with EDTA at pH 5.5.
The effective formation constant of the Zn-EDTA complex
is 106 above pH 4 (3). Xylenol Orange is used as an indicator; it is yellow when it is free and red when complexed
with zinc. A competition is set up between EDTA and the
indicator. When all of the zinc ions have been complexed
with EDTA, only the free indicator remains, causing a
change in color from pink to yellow.
Cold-Eeze cold lozenges are a product designed to
reduce the duration and severity of the common cold
through the actions of ionic zinc in the mouth, throat and
nasal cavity (48). Therefore, the zinc ions must be quantitatively released from the cold lozenges into saliva. Analytical
studies have shown that 93% of the zinc ions are released
into saliva (9). However, EDTA is a much stronger complexing agent that any other ingredient in the lozenges, and can
be used to quantitatively determine zinc content. The cold
lozenges are designed to be slowly dissolved in the mouth
where the pH of saliva is on average 5.5. For this reason,
the titrations are performed at that pH. The cold lozenges
also contain gluconate, glycine, and a hard candy base. The
theoretical amount of zinc per lozenge is 11.5 mg or 14.5
mg, depending on the type of lozenge. Amounts of zinc per
lozenge are printed on the packages.

3. Prepare the EDTA solution by weighing 0.93 g of

dry Na2 EDTA2H2O into a 250-mL volumetric flask and
diluting to the mark. Deduce the actual molarity assuming
that the EDTA is pure.
4. Perform each titration as follows: Dissolve one cold
lozenge in 50.0 mL of buffer; gentle heating may be necessary. Cool to room temperature. (Optional: measure the pH
of the resultant solution.) Prepare a blank solution to
determine the endpoint color. Add a few drops of Xylenol
Orange solution and titrate with EDTA solution to the endpoint. Use one titration to determine the endpoint and carefully complete three additional titrations.
Results from analyses of lozenges by this method have
yielded consistent data. For the 14.5-mg lozenges, 108
analyses had an average of 14.33 mg zinc with a standard
deviation of 0.74, and 119 analyses of the 11.5-mg lozenges
had an average of 11.58 mg zinc with a standard deviation
of 0.62. This is well within the FDA guideline of 90120%
of the theoretical amount.
This experiment is straightforward and easy to perform,
giving students experience in buffer preparation and EDTA
titration. The endpoint is crisp with a visible change of color.
Students are given the opportunity to analyze a marketed
product in the same way as is used by the manufacturers.
Students can consider themselves the quality control chemists for the manufacture of these cold lozenges. They can compare the average milligrams of zinc to the expected amount
and comment on the consistency of manufacture.
I wish to acknowledge John C. Godfrey and NancyJane
Godfrey for analytical results.

Experimental Procedure

1. Order product directly by calling 1-800/505-COLD.

2. Xylenol Orange is available from Aldrich Chemical Co.,
product # 22,785-4. The author has found that solutions made with
pure Xylenol Orange perform better than those prepared from a
prepackaged mixture of Xylenol Orange and NaCl (diluent).


Literature Cited

1. Cold-Eeze cold lozenges (Quigley Corporation,

Doylestown, PA)1
2. pH 5.5 acetate buffer
3. Xylenol Orange indicator (0.1% solution in DI water)2
4. 0.01 M Na 2EDTA solution

1. Dry Na2 EDTA2H2O for about one hour in the oven;
cool in a desiccator.
2. Prepare the pH 5.5 buffer by combining 1.35 g of
glacial acetic acid (C AUTION!) and 10.25 g of sodium acetate
(or 17.01 g of sodium acetate trihydrate) in a 250-mL volumetric flask and diluting to the mark. Adjust pH to 5.5 with
either 6 M NaOH or glacial acetic acid.

1. Day, R. A., Jr.; Underwood, A. L. In Quantitative Analysis, 6th ed.;

Prentice Hall: Englewood Cliffs, NJ, 1991; pp 623624.
2. Harris, D. C. In Quantitative Chemical Analysis; 4th ed.; W. H.
Freeman: New York, 1995; pp 793794.
3. Harris, D. C. In Quantitative Chemical Analysis; 4th ed.; W. H.
Freeman: New York, 1995; p 323.
4. Al-Nakib, W.; Higgins, P. C.; Barrow, I.; Batstone, G.; Tyrell, D. A.
J. Antimicrob. Chemother. 1987, 20, 893901.
5. Godfrey, J. C. Antimicrob. Agents Chemother. 1988, 32, 605606.
6. Godfrey, J. C.; Conant-Sloane, B.; Turco, J. H.; Mercer, N.; Godfrey,
N. J.; Smith, D. S. In ICAAC; Chicago, 1991; Abs. No. 1381.
7. Godfrey, J. C.; Conant-Sloane, B.; Smith, D. S.; Turco, J. H.; Mercer, N.; Godfrey, N. J. J. Int. Med. Res. 1992, 20, 234246.
8. Godfrey, J. C.; Godfrey, N. J.; Novick, S. G. Alternative Therapies
1996, 2(6), 6372.
9. Zarembo, J. E.; Godfrey, J. C.; Godfrey, N. J. J. Pharm. Sci. 1992,
81, 128130.

Vol. 74 No. 12 December 1997 Journal of Chemical Education