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RECOMMENDATIONS FOR HEXAVALENT CHROMIUM SAMPLE <br /> COLLECTION AND PRESERVATION <br /> The method DHS specifies for the determination of Cr(VI) in drinking water is EPA <br /> method 218.6 "Determination of.Dissolved Hexavalent Chromium in Drinking Water, <br /> Groundwater, and Industrial Wastewater Effluents by Ion Chromatography". As <br /> indicated in the title,this method was originally devised to be applicable to a broad range <br /> of aqueous samples, including industrial wastewaters, i.e., it was not primarily intended <br /> for the analysis of drinking water. As such, the method provides some latitude in terms of <br /> sample preservation and pretreatment, stipulating that consideration should be given to <br /> the type of data required. <br /> Considering the specific situation with drinking water, the Department provides the <br /> following guidance with regard to sample filtration,pH adjustment, and sample <br /> transportation and storage: <br /> (1) Filtration of samples immediately following sample collection is not recommended. <br /> Drinking water samples are typically low in particulate matter and performing filtration <br /> in the field without the potential of adsorption losses and/or contamination is difficult. <br /> Filtration of drinking water samples is also not performed in the determination of other <br /> trace metal contaminants. Filtration of samples immediately prior to the ion chromato- <br /> graphic determination is recommended in order to protect the analytical instrumentation, <br /> v i.e., to avoid premature clogging of the guard column. <br /> (2) Immediately following collection, the pH of samples should be adjusted to the range <br /> 9.0-9.5 in order to minimize the potential loss of Cr(VI) through chemical reduction. <br /> With some water samples it may be difficult to ieve-the- s' pH with the <br /> ammonium sulfate/hydroxide buffer prescribed'by.EPA 218.6 (e.g.,--�olorado River <br /> water) without adding so much sulfate that the subsequent ion chror{atographic analysis <br /> is compromised through analytical column overloading. For water samples exhibiting this <br /> problem, the Department suggests the use of a modified pH-adjustment buffer that <br /> contains ten times less ammonium sulfate (33 g/L)but the same concentration of <br /> ammonium hydroxide as the buffer prescribed in EPA 218.6. It should be noted however, <br /> that at the present time the Department does not have sufficient data to determine whether <br /> this modified buffer is adequate for all types of drinking water samples. <br /> (3) Samples must be cooled to 4 °C during transport and storage and analyzed within 24 <br /> hours of collection. <br /> SCREENING FOR HEXAVALENT CHROMIUM USING TOTAL CHROMIUM <br /> ANALYSIS <br /> The Department's present DLR for Cr(VI) is 1 µg/L This value was originally derived <br /> from a single-laboratory MDL of 0.2 gg/L using a multiplier of five. In order to be <br /> consistent with the DLR for Cr(VI) of 1 gg/L, any analytical technique for measuring <br /> total chromium which is to serve as a screening tool for Cr(VI) must be capable of <br /> UCMR Guidance,January 30,2001 Page 3 <br />