METHOD 552 DETERMINATION OF HALOACETIC …

1 552-1 METHOD 552 DETERMINATION OF HALOACETIC ACIDS IN DRINKING WATER BY LIQUID-LIQUID extraction , derivatization , AND GAS CHROMATOGRAPHYWITH electron capture DETECTIONJuly 1990 Jimmie W. HodgesonJ. Collins (Technology Applications Inc.) Barth (Technology Applications Inc.)ENVIRONMENTAL MONITORING SYSTEMS LABORATORYOFFICE OF RESEARCH AND ENVIRONMENTAL PROTECTION AGENCYCINCINNATI, OHIO 45268552-2 METHOD 552 DETERMINATION OF HALOACETIC ACIDS IN DRINKING WATER BY LIQUID-LIQUID extraction , derivatization , AND GAS CHROMATOGRAPHYWITH electron capture AND is a gas chromatographic (GC) METHOD applicable to the determination1-4,11of the listed halogenated acetic acids in drinking water, ground water, rawwater and any intermediate treatment stage.

2 In addition, the chlorinatedphenols listed may be analyzed by this NumberChemical Abstract ServicesMonochloroacetic Acid79-11-8 Dichloroacetic Acid79-43-6 Trichloroacetic Acid76-03-9 Monobromoacetic Acid79-08-3 Bromochloroacetic Acid5589-96-3 Dibromoacetic Acid631-64-12,4-Dichlorophenol120-83-22, 4, METHOD is applicable to the DETERMINATION of these analytes over theconcentration ranges typically found in drinking water, subject to the1,2,4method detection limits (MDL) listed in Table 2. The detection limits observedmay vary according to the particular matrix analyzed and the specificinstrumentation employed.

3 The HALOACETIC acids are observed ubiquitously inchlorinated supplies at concentrations normally within the spiking level rangesin Tables acid has not been included because of problems with extractionand chromatography by this METHOD . The mixed bromochloroacetic acids haverecently been synthesized. The bromochloroacetic acid is present inchlorinated supplies and METHOD validation data are provided herein. However, neat material for this compound is not readily available. The mixedtrihalogenated acids may also be present.

4 These are not included because ofcurrent problems with sample purity and the chromatography for these 2-chlorophenol has not been included as a METHOD analyte in the abovelist, primarily because its realistic detection limit in environmental samples islikely to be above the odor threshold. Poor precision is usually obtained forthis compound at even higher levels. In addition, this analyte displays552-3instability under the dechlorination/preservation conditions described herein. Nevertheless, some METHOD validation data are given in Tables METHOD is designed for analysts skilled in liquid-liquid extractions, extractconcentration techniques, derivatization procedures and the use of GC andinterpretation of gas this METHOD is used for the analyses of waters from unfamiliar sources,analyte identifications must be confirmed by at least one additional qualitativetechnique, such as GC/mass spectroscopy (MS)

5 Or by GC using OF 100 mL volume of sample is adjusted to pH and extracted with methyl-tert-butyl ether (MTBE) to remove neutral and basic organic compounds. Theaqueous sample is then acidified to pH and the acids are extracted intoMTBE. After the extract is dried and concentrated, the acids are converted totheir methyl esters with diazomethane (DAM). Excess DAM is removed andthe methyl esters are determined by capillary GC using an electron capturedetector (ECD). An alternative microextraction procedure is also offered inwhich a 30 mL sample is extracted without cleanup with a single 3 mL aliquotof MTBE for direct analysis by GC-ECD after methylation.

6 Samples containinghigh concentrations of HALOACETIC acids and other disinfection byproducts, orother potentially interfering organic compounds, may require the Standard -- A pure analyte(s) added to a solution in known amount(s)and used to measure the relative responses of other METHOD analytes andsurrogates that are components of the same solution. The internal standardmust be an analyte that is not a sample Analyte -- A pure analyte(s), which is extremely unlikely to befound in any sample, and which is added to a sample aliquot in knownamount(s) before extraction and is measured with the same procedures used tomeasure other sample components.

7 The purpose of a surrogate analyte is tomonitor METHOD performance with each Duplicates (LD1 and LD2) -- Two sample aliquots taken in theanalytical laboratory and analyzed separately with identical of LD1 and LD2 give a measure of the precision associated withlaboratory procedures, but not with sample collection, preservation, or Duplicates (FD1 and FD2) -- Two separate samples collected at the sametime and place under identical circumstances and treated exactly the samethroughout field and laboratory procedures.

8 Analyses of FD1 and FD2 give ameasure of the precision associated with sample collection, preservation andstorage, as well as with laboratory Reagent Blank (LRB) -- An aliquot of reagent water that is treatedexactly as a sample including exposure to all glassware, equipment, solvents,reagents, internal standards, and surrogates that are used with other samples. The LRB is used to determine if METHOD analytes or other interferences arepresent in the labora-tory environment, the reagents, or the Reagent Blank (FRB) -- Reagent water placed in a sample container in thelaboratory and treated as a sample in all respects, including exposure tosampling site conditions, storage, preservation and all analytical purpose of the FRB is to determine if METHOD analytes or otherinterferences are present in the field Fortified Blank (LFB)

9 -- An aliquot of reagent water to whichknown quantities of the METHOD analytes are added in the laboratory. The LFBis analyzed exactly like a sample, and its purpose is to determine whether themethodology is in control, and whether the laboratory is capable of makingaccurate and precise measurements at the required METHOD detection Fortified Sample Matrix (LFM) -- An aliquot of an environmentalsample to which known quantities of the METHOD analytes are added in thelaboratory. The LFM is analyzed exactly like a sample, and its purpose is todetermine whether the sample matrix contributes bias to the analytical background concentrations of the analytes in the sample matrix must bedetermined in a separate aliquot and the measured values in the LFMcorrected for background Standard Solution -- A concentrated solution containing a single certifiedstandard that is a METHOD analyte.

10 Or a concentrated solution of a singleanalyte prepared in the laboratory with an assayed reference compound. Stockstandard solutions are used to prepare primary dilution Dilution Standard Solution -- A solution of several analytes preparedin the laboratory from stock standard solutions and diluted as needed toprepare calibration solutions and other needed analyte Standard (CAL) -- A solution prepared from the primary dilutionstandard solution and stock standard solutions of the internal standards andsurrogate analytes.