determination of iron in water

1. Determination of Iron in Water CHEM3550

3. Part A The test for the thiocyanate ion is to add iron (III) nitrate to a solution. If the solution turns blood-red upon the addition of iron(III) nitrate this indicates the presence of the thiocyanate ion Fe3+(aq) + 6 SCN-(aq) ? [Fe(SCN)6]3-(aq) http://www.meta-synthesis.com/webbook/15_redox/redox.htmlhttp://www.meta-synthesis.com/webbook/15_redox/redox.html

4. Chemistry Reduction of iron: 2Fe3+(aq) + 2NH2OH(aq) + 2OH-(aq) ? 2Fe2+(aq) + N2(g) + 4H2O(l) Complexation by 1,10-phen Fe2+(aq) + 3(C12H2N2)3(aq) ? [(C12H2N2)3Fe]2+(ag)

5. [(C12H2N2)3Fe]2+

6. Questions What is a chromophore? Why is it necessary to wait 10 minutes before reading the spectrophotometer? 3. What is a chelating agent? (a) The standard recipe used in this exercise uses 3.0 mL of 0.25% o- phenanthroline solution in 100mL of final solution to generate the red iron- phenanthroline complex which is determined colorimetrically. What is the initial molarity of o-phenanthroline in the diluted solution? [0.25% means 2.50 g. of o- phenanthroline (molar mass 180) per liter of solution.] (b) What is the maximum concentration of iron-phenanthroline complex that can be formed from this amount of o-phenanthroline, assuming complete complexation? (c) What does this concentration of iron correspond to in mg/L? (d) Is this enough for the amounts of iron (up to 20mL of stock solution) we are using? (i.e.: What is the limiting reagent in these reactions?) (a) The standard recipe used in this exercise uses 3.0 mL of 0.25% o- phenanthroline solution in 100mL of final solution to generate the red iron- phenanthroline complex which is determined colorimetrically. What is the initial molarity of o-phenanthroline in the diluted solution? [0.25% means 2.50 g. of o- phenanthroline (molar mass 180) per liter of solution.] (b) What is the maximum concentration of iron-phenanthroline complex that can be formed from this amount of o-phenanthroline, assuming complete complexation? (c) What does this concentration of iron correspond to in mg/L? (d) Is this enough for the amounts of iron (up to 20mL of stock solution) we are using? (i.e.: What is the limiting reagent in these reactions?)

7. Making the Standard Fe Solution To determine ppm iron, you need to know that ferrous ammonium sulfate is Fe(NH4)2(SO4)2 �6H2O and has a molecular weight of 392.14 g/mol. Note that ferrous ammonium sulfate is sometimes abbreviated as �FAS� First calculate the % Fe in FAS (= 55.84/392.14 = 14.24 %) Then divide the desired conc. by the % Fe in this compound: 100 ppm standard required: 100 mg Fe per liter = 702 mg FAS / L 55.84/392.14 = 351 mg FAS in 500 mL

8. Method NOTE: All iron solutions should be discarded into a �Heavy Metal� waste container. 1. Obtain your unknown. 2. Standard 100 ppm Fe Solution: Obtain 100 mL of 100 ppm stock ferrous ammonium sulfate (Fe(NH4)2(SO4)2 �6H2O) solution (351 mg in 500 mL) in a clean conical flask. Be certain to note the mass of ferrous ammonium sulfate used and the final volume of the solution. 3. Preparation of stds: Prepare five standard solutions of iron (II) having the following concentrations 0 (reagent blank), 0.5, 1.0, 2.0, and 5.0 ppm. Pipette 0.5, 1, 2 and 5 mL aliquots of the standard iron solution into 100 mL volumetric flasks and dilute to the mark with DI water. Obtaining a Beer�s Law Plot: Transfer a 5 mL aliquot of the 0.5 ppm iron standard to a 125 mL flask and test the pH with test paper. If greater than 4.5, add enough 0.2 M sulfuric acid dropwise to bring the pH to about 3.5, counting the number of drops. Again counting drops, add sodium citrate (259 g/L) buffer to bring the pH to about 4.5. Pipet 1 mL of 10% hydroxylamine hydrochloride and 3 mL of 1,10-phenanthroline into the sample, mix, and allow 5 minutes for color development. DO NOT PUT YOUR PIPETTES INTO THESE SOLUTIONS; pour a small amount into your beaker and pipette from this. Be sure to add the reagents in the order shown here. Use the same number of drops of sulfuric acid and sodium citrate for the remaing standards, followed by 1 mL of 10% hydroxylamine hydrochloride and 3 mL of 1,10-phenanthroline. 6. Adjust the spectrometer to 512 nm, allow 30 mins for the instrument to warm up. Using DI water as the reference blank to zero the instrument, measure the absorbance of each standard (including the reagent blank) 7. Analysis of Samples: Natural and tap water samples often have less than 0.5 ppm iron. Determine the iron in several environmental samples. Treat samples the same way as the standards, adding sulfuric acid initially, if necessary, followed by citrate buffer, reducing agent and indicator. Use 5 mL samples and adjust the pH for each sample individually. Dissolve 0.7022 grams of ferrous ammonium sulfate, hexahydrate in distilled water. Dilute to 1.00 L. This solution is 100 mg/L Fe+2 (same as 100 ppm).Dissolve 0.7022 grams of ferrous ammonium sulfate, hexahydrate in distilled water. Dilute to 1.00 L. This solution is 100 mg/L Fe+2 (same as 100 ppm).

9. Calculations Notes: 1. Draw a calibration curve, then perform a best-fit line of your data without forcing the line through the origin. Outline of Calculations: Describe how the 100 ppm Fe standard solution was made. You need to do dilution calculations for each individual iron standard solution, seeking to determine the concentration of the final solution (as tested in the spectrometer) in ppm Fe (mg Fe /L). The basic equation is C1 x V1 = C2 x V2 3. Use the calculated concentrations of the diluted standards as the x values for graphing your calibration curve, paired with the absorbance values (as the y value) for those solutions. Use the equation of your best fit line on the calibration curve to determine the concentration of iron (in ppm Fe) in your unknown sample. Use correct sig. figs. That value (the concentration of iron in the diluted solution, as measured in the spectrometer is the final value you are expected to report. If duplicate determinations were done, report both individual and average values.

10. A = ebc

11. Questions 1. Why use a �reagent blank� and not just distilled water to zero the spectrometer? 2. What would the effect be of waiting 30 minutes instead of 5 minutes for step 4? 3. Today�s unknown samples are simple iron dissolved in water. If our sample were more complex, it might contain other compounds, some which might be colored, including some which might absorb light at the same wavelength as the iron phenanthroline complex. What problem would this cause? How could we modify our procedure to correct for this problem? 4. State the function of each reagent in this experiment: 1,10-phenanthroline, hydroxylamine hydrochloride, sodium citrate. 5. For the instrument you used, what would you estimate to be the lowest concentration of iron that would be reliable? 1. To minimize effects of interfering species. 4. 1,10-Phen complexes Fe2+, Hydroxylamine hydrochloride reduces ferrous to ferric ions. Sodium acetate buffers to pH 3.51. To minimize effects of interfering species. 4. 1,10-Phen complexes Fe2+, Hydroxylamine hydrochloride reduces ferrous to ferric ions. Sodium acetate buffers to pH 3.5

12. Field Instrumentation Palintest - Ferrometer 1000 1,10 phenanthroline test 0.02 to 5.00 mg/L Fe http://www.palintestusa.comhttp://www.palintestusa.com

13. References E. B. Sandell, Colorimetric Determination of Traces of Metals, 3rd Ed. Interscience Publishers, Inc., New York, 1959. D. A. Skoog, D. M. West, F. J. Holler, and S. R. Crouch, Analytical Chemistry: An Introduction, 7th ed., Chapters 21 and 22, pp. 547-592.