EPA 525.2 PDF

EPA 525.2 PDF

Application Note US EPA Method — Determination of. Semivolatile Organics in Water by Solid-Phase. Extraction and GC/MS Detection. IntroductIon. Bromacil. EPA Method Revision Determination of Organic Compounds in Drinking Water by. Liquid-Solid Extraction and Capillary Column. Organic Compounds Analysis in Drinking Water (EPA ) by GC (TN). Abstract: The accepted levels of compounds allowed in drinking water are.

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A method detection limit MDL must be determined for each analyte.

Precision and accuracy values were generated primarily from 8 replicate analyses of fortified reagent water using a liquid-solid C extraction cartridges and a quadrapole mass spectrometer see Table 3 of the Method. Fri Dec 09, 8: That could be the problem. I’ll also try to keep the lights out a bit and see if that helps too. Thu Nov 05, 3: We use an automated system setup of Horizon extractors atlantic C18 disks and a Horizon Dry Vap for drying and concentration.

We didn’t used to have this problem and are now starting to see this happening in our The method contains a large amount of additional information.

Kelso, Washington 55.2 Method information displayed is provided for informational purposes only. Since the method states “less than a pH of 2” most of our collectors overkill on the HCl. Organic compounds – Instrument used for this test: All of the PAHs are a little low, how light sensitive are they? Latest Blog Posts from Separation Science.


EPA Method 525.2

This method provides procedures for the determination of a wide range of organic compounds found in finished drinking water, source water, or drinking water in any treatment stage. Initial demonstration of laboratory capability followed 5225.2 regular analyses of laboratory reagent blanks LRBslaboratory fortified 525.22 LFBsand laboratory fortified matrix samples. So we installed less intensive lights and tried to do the extraction in the dark as much as possible which solved our problem.

For these pea analytes 8 replicate reagent water samples were analyzed, except for PCB 6 replicates and toxaphene 7 replicatesand except for bis 2-ethylhexyl phthalate and di-n-butyl phthalate for which 7 replicates of fortified tap water were analyzed. Does anyone have any ideas on where this maybe happening?????

Analyte Loss EPA – Chromatography Forum

I have tried adding preservative sodium sulfite and altering the amount of 1: Mon Jan 07, 8: I have tried bypassing the dry vap as well as spiking before the dry vap and get similar results. Analyte CAS Number 1,3-Dimethylnitrobenzene Acenaphthene-d10 Alachlor Atrazine Benzo a pyrene Bis 2-ethylhexyl Adipate Bis 2-ethylhexyl Phthalate Chrysene-d12 Hexachlorobenzene Hexachlorocyclopentadiene Perylene-d12 Phenanthrene-d10 Simazine Triphenyl Phosphate Examples: We adjust the QC to match the samples which are always more spa than 2.


This is why I think it’s in the extraction. How long have your PAH recoveries been low? B Contamination from sample carryover: We use a hydrophobic membrane on the dry vap to dry the sample. My dperylene along with the benzo a pyrene is also a major problem. Wed Jan 04, 2: If you weren’t the lowest bid, we don’t get to play with your eqiupment.

Thu Mar 03, 8: Extracts can be held up to 30 ela. Please add to the discussion any other ideas you may have. Organic compound analytes, internal standards, and surrogates are extracted from a 1L sample by passing it through a disk or cartridge containing a solid matrix with a chemically bonded C18 organic phase [liquid-solid extraction LSE ].

I haven’t tried to avoid light although our sample bottles and chromatography vials are all amber glass. Separation Science offers free learning from the experts covering methods, applications, webinars, eSeminars, videos, tutorials for users of liquid chromatography, gas chromatography, mass spectrometry, sample preparation and related analytical techniques.

Mon Mar 28, 5: I’m not sure what changed. We actually don’t use sodium sulfate to dry.

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