PHOSPHATE DETERMINATION
Range = 0.03 to 5.00g-at/L
I. REAGENTS AND STOCK SOLUTIONS REQUIRED:
- Ammonium Molybdate sol’n:
Dissolve 7.5g of ammonium paramolybdate (NH4)Mo7O24-4H2O in 250mL of DI water. Store in plastic bottle out of sunlight.
- Sulfuric Acid Sol’n:
Add 70mL of concentrated sulfuric acid to 450mL of DI water. Allow the solution to cool and store it in a glass bottle.
- Ascorbic Acid Solution:
Dissolve 13.5g of ascorbic acid in 250mL of DI water. Store the solution in a plastic bottle in the freezer. This solution should not be kept at room temperature for more than one week, but is stable in the freezer for many months.
- Potassium antimonyl-tartrate solution:
Dissolve 0.34g of potassium antimonyl-tartrate in 250mL of DI water (if necessary, warm and use a stirring rod to help dissolve). Store in a plastic bottle.
- Mixed Reagent:
Mix together 100mL ammonium molybdate, 250mL sulfuric acid, 100mL ascorbic acid, and 50mL of potassium antimonyl-tartrate solutions. Prepare this solution fresh as needed. Quantity is suitable for about 50 samples. Discard excess.
- Phosphate Primary Stock:
Prepare a 10mM solution. Weigh out 0.6805g of KH2PO4 (fw = 136.09). Dissolve in distilled, deionized water, making up to 100mL using a volumetric flask.
- Phosphate Secondary Stock:
Prepare a 50M solution. Bring 100 uL of the primary stock up to 100mL with distilled, deionized water using a volumetric flask.
- Synthetic Seawater:
Mix together 31g NaCl, 10g MgSO4, and 0.5g Sodium Bicarbonate in 1000mL distilled water.
II. BLANK DETERMINATION
Use synthetic seawater in place of a sample and carry out the steps outlined in section IV to obtain the turbidity and extinction of the reagent blank. Reagent blanks should be less than 0.02 in a 5cm cell.
III. STANDARDS
Phosphate Conc. (M) / Phosphate 2º Standard (mL) / Synthetic Seawater0.05 / 0.10 / ADD
0.10 / 0.20 / TO
0.50 / 1.00 / MAKE
0.75 / 1.50 / 100mL
1.00 / 2.00 / FINAL
1.50 / 3.00 / VOLUME
2.00 / 4.00
For example, to make a 0.1mM phosphate solution, add 0.20mL of the phosphate secondary standard to a 100mL volumetric flask, then raise the volume to 100mL with synthetic seawater.
Carry out the steps outlined in section IV (2-5) to obtain the extinction of the standards.
Plot the concentration of the standards vs. the measured absorbance and perform a linear regression to obtain a standard curve.
IV. PROCEDURE
- Warm the samples to room temperature. Using a spectrophotomer, measure the turbidity of a sample at 885nm (using a a 5cm cell against DI water). If this value is greater than 0.01, a correction should be applied to the final extinction value.
- Measure out 100mL of sample using a graduated cylinder
- add 10mL of the mixed reagent, using a volumetric pipette, and mix.
- Wait at least 5 minutes (and not more than 2-3 hours)
- Measure the extinction in a 5cm cell against DI water at 885nm. Correct the absorbance measurement by subtracting the value obtained for the blank.
- Use the standard curve to determine the concentration of your unknown.