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A guide to our Lab Work
Preparation of Standard solutions
Standard solutions were prepared in 50cm3 volumetric flasks labelled from A to F. All solutions contained 5cm3 of 5% Ethanoic Acid, 5cm3 of 2% KI and varying amounts of Diluted Milton Reagent as outlined in Table
Samples of these solutions were placed in cuvettes and placed in the Colorimeter; the absorbance values were read and a calibration curve produced.
At this stage we proceeded to extract the Iodide from the food samples.
Analysis of Iodide in Food Samples.
1. Removal of interfering Pigments.
From this list it is obvious that some of the samples (Broccoli, Carrots, Kelp, Cauliflower) contained pigments that would interfere with the identification of the Iodide pigment, as a result we removed these interfering pigments by extracting them in Methylated spirits, using the same procedure used to extract Chlorophyll from a green leaf. We felt that this procedure would not affect our overall analysis, since the iodide ion I- is polar and it would not be extracted in the non-polar solvent Methylated spirits. (Likes dissolve likes).
2. Extraction of Iodide from food Samples.
Using the principle of Likes dissolves Likes as used above we extracted the Iodide from the food samples using water. Solid food samples were liquefied using a food processor and water was added (in known quantities) to improve the texture of the sample to make it suitable for reading using the colorimeter.
Volumetric Analysis to determine the concentration of Diluted Milton Solution.
In order to determine the precise concentration of the hypo chlorite ion (diluted Milton Reagent) we performed a volumetric analysis using a 0.12M standard solution of sodium thiosulphate. The reaction occurs according to the following equations:
ClO- + 2I- + 2H+ goes to Cl- +I2 + H20
2 S203- + I2 goes to S406 - + 2I-
The end point was determined using a starch indicator, which was added to the conical flask when the solution turned a straw yellow colour; on addition of the starch the contents of the flask became a blue/black colour. The titration was continued until the blue/black colour disappeared.