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Spectrophotometric Determination of Iron in Dietary Supplements For CHM 122.2
Spectrophotometric Determination of Iron in Dietary Supplements For CHM 122.2
Activity 1
Introduction
The reaction between iron(II) ion and 1,10-phenanthroline to form a red complex
serves as a good sensitive method for determining iron. The molar absorptivity of the complex
[(C12H8N2)3Fe]2+, is 11,000 at 508 nm. The intensity of the color is independent of pH in the
range 2 to 9. The complex is very stable and the color intensity does not change appreciably
over very long period of time. Beer’s law is obeyed.
The iron must be in the +2 oxidation state, and hence a reducing agent is added before
the color is developed. Hydroxylamine, as its hydrochloride, can be used, the reaction being
2Fe3+ + 2NH2OH ➔ 2Fe2+ +N2 + H2O
The pH is adjusted to a value between 6 and 9 by addition of ammonia or sodium acetate. An
excellent discussion of interferences and of applications of this method is given by Sandyll.
OBJECTIVE:
Any solution containing the red Fe–1,10-phenanthroline complex should be disposed of in the
appropriately labeled container. All other waste can be disposed of down the drain
Reagents:
a. 0.2 % of 1,10- phenanthroline; Dissolve 0.1g of 1,10-phenanthroline in 100mL distilled
water
b. 6 M hydrochloric acid; Transfer 100ml 12M HCl to 100mL distilled water and stir to
mix. Transfer the resulting solution to a clean and labelled reagent bottle
c. 10 % sodium acetate; Dissolve 10 grams of sodium acetate in 100mL water
10 % hydroxylamine hydrochloride; Dissolve 10g hydroxylamine hydrochloride in
100mL distilled water.
d. Ferrous ammonium sulfate hexahydrate, 100mgFe/Li
Weigh accurately about 0.0700g of pure ferrous ammonium sulfate, dissolve in water,
and transfer the solution to a 100-mL volumetric flask. Add 2.5mL sulfuric acid and
dilute it o the mark.
Procedure
1. Purchase two brands (5 tablets per type) of iron supplementary tablets.
2. Weigh the 5 tablets (each type) in an analytical balance and record the mass in your
data notebook.
3. Manually ground the tablets using an agate Mortar and pestle and pass the ground
materials in 200 mesh filter to obtain fine powder. Place the fine powder in a clean
and labelled vial and store it in a desiccator.
4. In three replicates, transfer 0.10xx g of the fine powder into 100mL beaker and boil
gently in a fume hood with 25mL of 6M HCl for about 15 minutes. Cover the beaker
with a watch glass (Atkins 1975).
5. When necessary, add distilled water (or deionized water) to keep a constant volume
of 15mL.
6. When digestion is finished, cool the beaker containing the digested sample. Rinsed
the watch glass with distilled water, and then filter the solution using Whatman-40
filter paper. Collect the filtrate in 250mL volumetric flask.
7. Rinse the residue remaining in the filter paper using deionized water and complete
the volume using distilled water.
8. Label the solution as “Stock sample solution”.