EPA METHOD 508A PDF

This kit provides all of the necessary materials to conduct the EPA A test. It can be used to analyze finished drinking water, drinking water in any stage for. EPA Method a – Screening for Polychlorinated Biphenyls by Perchlorination and Gas Chromatography. Analyzer Description. Configuration: 1-capillary. Subsequently, the LabCert program has only offered certification for the analysis of PCBs in drinking water by EPA method A. Method A, and s.

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Changes were made in the recommended chromatographic conditions and internal standards in Method If sample extract continues to fail the recovery criterion, report all data for that sample as suspect. The remaining SbCl5 will react exothermally with the HC1. Peak tailing significantly in excess of that shown in the method chromatogram Figure 3 must be corrected. Transfer the solvent to the separatory funnel and extract the sample by vigorously shaking the funnel for 2 min with periodic venting to release excess pressure.

Analyze SE-1 in duplicate, then proceed to 9. Transfer the solvent to the sample contained in the separatory funnel or tumbler bottle, seal, and shake for 10 s, venting periodically.

Screw cap culture test tubes — mm x 13 mm i. If the repetition also fails, a new calibration curve must be generated for that analyte using freshly prepared standards.

Quality Control QC Sample — A sample containing known concentrations of analytes that is analyzed by a laboratory to demonstrate that it can obtain acceptable identifications and measurements with procedures to be used to analyze environmental samples containing the same or similar analytes.

If within the retention time window of any analyte the LRB produces a peak that would prevent the determination of that analyte, determine the source of contamination and eliminate the interference before processing samples.

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EPA Method 508A Screening for Polychlorinated Biphenyls by Perchlorination

Ascorbic acid has been extensively tested as a dechlorinating agent, and has been found to be as effective as sodium thiosulfate, but without the undesirable generation of sulfur dioxide at low pH.

No 058a bubbles should pass through the sample as the bottle is filled, or be trapped in the sample when the bottle is sealed.

All reagents and apparatus must be routinely demonstrated to be free from interferences under the conditions of the analysis, by running laboratory reagent blanks as described in Sect. Pour the entire sample epw a 2-L separatory funnel.

The analyst must further demonstrate that the measurement of the internal standard is not affected by method or matrix interferences.

Check with suppliers for a suitable substitute if this material cannot be located. The column is temperature programmed to separate the method analytes which are then detected with a photoionization detector PID and a halogen specific detector placed in series.

Decachlorobiphenyl, A / Reference Standards / Chromatography Products at

If the emulsion interface between layers is more than one third the volume of the solvent layer, the analyst must employ mechanical techniques to complete the phase separation.

Analytes that are inefficiently purged from water will not be detected when present at low concentrations, but they can be measured with acceptable accuracy and precision when present methoc sufficient amounts.

A second LFB containing each analyte that failed must be analyzed. After approximately seven min, turn off the trap heater and open the syringe valve to stop the gas flow through the trap. Individual vials shown to contain at least Add preservative to blanks and QC check standards. If the value for the DCB is 0.

Samples not analyzed within this period must be discarded and replaced. Analytical Balance — Capable of accurately weighing to 0. The columns used in this method may well be adequate, however, no data were collected for these constituents during methods development. While some of these methods may provide reliable results with more complex water matrices, for example, industrial wastewaters and beverages, techniques for dealing with more complex matrices have not been included in the methods in order to keep them as simple and brief as possible.

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Distilled water met this criterion.

Additional information on laboratory safety is available Quantitatively transfer the extract to a mm x 13 mm i. Add mg of iron powder to the extract. Concentrate the extract to about 0.

Peak tailing significantly in excess of that shown in the method chromatograms Figures 6 and 7 must be corrected.

Aldrin, hexachlorocyclopentadiene and methoxychlor are rapidly oxidized by chlorine. PIand other suppliers. The extent of matrix interferences will vary considerably from source to source depending upon the water sampled. An explosion shield should be used during the perchlorination and neutralization procedures along with additional eye protection such as an 8-in. The background concentrations of the analytes in the sample matrix must be determined in a separate aliquot and the measured values in the LFM corrected for background concentrations.

Since methylene chloride mrthod permeate through PTFE tubing, all gas chromatography carrier gas lines and purge gas plumbing should be constructed from stainless steel or copper tubing. Laboratory Fortified Sample Matrix LFM — An aliquot of an environmental sample to which known quantities mehod the method analytes are added in the laboratory.

After cooling, store glassware inverted or covered with aluminum foil. If within the reten- tion time window of any analyte the LRB produces a peak that would prevent the determination of that analyte, determine the source of contamination and eliminate the interference before processing samples.