EPA-NERL: 365.5: Orthophosphate in Estuarine and Coastal Waters by Colorimetry
Official Method Name
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Determination of Orthophosphate in Estuarine and Coastal Waters by Automated Colorimetric Analysis |
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Current Revision
| Revision 1.4, September 1997 |
Media
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WATER |
Instrumentation
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Automated Spectrophotometer |
Method Subcategory
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Inorganic |
Method Source
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Citation
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Brief Method Summary
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This method is based on the method of Murphy and Riley. A sample is introduced into an automated segmented flow analyzer. Orthophosphate reacts with ammonium molybdate and ammonium potassium tartrate in an acidic medium to form an antimony-phoso-molybdate complex. The complex is reduced using ascorbic acid, and the concentration of orthophosphate is determined by measuring the absorbance of the reduced complex with an on-line colorimeter. |
Scope and Application
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This method determines low-level orthophosphate concentrations in estuarine and coastal waters. |
Applicable Concentration Range
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The method is linear up to 0.39 mg-P/L |
Interferences
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(A) Hydrogen sulfide: Dilute samples with high sulfide contents to minimize interferences. (B) Turbidity: Remove turbidity using filtration. (C) Metals: High iron concentrations can precipitate phosphate. |
Quality Control Requirements
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Initial demonstration of performance, continued analysis of Laboratory Reagent Blanks (LRB), laboratory duplicates, and Laboratory Fortified Blanks (LFB) with each set of samples as a continuing check on performance. |
Sample Handling
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Samples collected using hydrocast or submersible pump systems. Turbid samples must be filtered through a 0.45 um membrane or glass fiber filter immediately after collection. Samples to be analyzed within 24 hours should be stored at 4oC until analysis. If samples cannot be analyzed within 24 hours, then freezing at -20oC for a maximum period of two months is acceptable. |
Maximum Holding Time
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24 hours; two months if stored at -20oC |
Relative Cost
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Less than $50 |
Sample Preparation Methods
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