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1 <br /> oxygen sensitive, the same precautions used for collection of DO samples should be followed <br /> (groundwater samples taken separately for ORP, measured ex situ). In dilute samples, it can take <br /> some time for the reading to be stabilize. minimize mixing to prevent oxygen introduction A <br /> flow-cell system will prevent mixing and minimize oxygen Interference. Redox probes can foul <br />' Nitrate <br /> Nitrate can be measured by colorunetnc methods, by use of a specific electrode, or by ion <br />' chromatography. Ion chromatography, a lab based method, is recommended. Although field <br /> colorimetric kits are available, the method Is sensitive to interference from dissolved constituents <br /> often found In groundwater. The presence of dissolved iron can give a false positive on the <br />' colorimetric method Nitrate concentrations can change due to bioactivity. Check with the <br /> analytical laboratory concerning the use of field preservatives. <br /> LSulfate <br /> Sulfate can be measured by colorimetric (field) methods or in the laboratory by ion <br /> chromatography. Due to potential interferences in the field methods for nitrate, it is probably <br /> best to measure sulfate and nitrate concurrently by the appropriate laboratory methods. Check <br />' with the analytical laboratory concerning the use of field preservatives. <br /> • <br /> Ferrous Iron <br />' In intrinsic evaluations, the form of Iron of interest is dissolved ferrous Iron (W). To separate <br /> the dissolved iron from precipitated iron, the sample should be filtered through a 0.45 micron <br />' filter immediately after collection. Time between collection and filtermg is Important si tre <br /> ferrous iron will react with oxygen and precipitate as ferric iron (Fe). If a pump is used for <br /> sample collection, an Inline filter should be considered. If total iron is required, a second non- <br /> filtered sample should also be collected. The sample should be stored In plastic bottles <br /> containing nitric acid as a preservative. All the samples containers and filters should be washed <br /> with a dilute nitric acid solution and rinsed with distilled water prior to taking into the field. <br /> Analysis should be done in the lab by TCP (Inductively Coupled Plasma). The concentration of <br /> other metals can be taken on the sample If required. <br /> HACH® colorimetric methods are available for ferrous and total iron. Since ferric iron does not <br /> react in the ferrous method, filtration Is not required unless the sample is turbid. If the sample is <br /> turbid it should be filtered through a 0.45 micron filter. In the total iron method all the iron is <br /> chemically reduced to ferrous iron and measured. Both these methods are pH sensitive. Follow <br /> the Instructions for controlling and measuring the pH. pH control is achieved by acidifying with <br /> hydrochloric acid. Correct the measured concentrations for the dilution caused by acid addition. <br /> Since ferrous Iron will oxidize and precipitate in the presence of oxygen, completely fill the <br /> . collection bottle to prevent headspace. Analyze the samples within six hours. <br />�J <br /> 11 <br />