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Donna L. Damrau

Publications and source records attributed to Donna L. Damrau.

2 recordsLinked to original sources

Methods of analysis by the U. S. Geological Survey National Water Quality Laboratory-Determination of organic plus inorganic mercury in filtered and unfiltered natural water with cold vapor; atomic fluorescence spectrometry

An analytical method using cold vapor-atomic fluorescence spectrometry was developed by the U.S. Geological Survey in 2001 for the determination of organic plus inorganic mercury in filtered and unfiltered natural water. This method was developed to eliminate the use of acid dichromate preservative and to provide capability to measure ambient mercury concentrations in natural water. Dissolved mercury includes all oxidizable mercury species present in natural water that has been filtered through a 0.45- micrometer pore size capsule filter. Wholewater recoverable mercury includes dissolved mercury species and mercury species adsorbed to particulate matter in unfiltered natural water. Mercury species can include elemental mercury, mercury (II), mercury (II) complexes, various alkyl- and phenylmercury compounds, and other forms of mercury. In this method, samples are collected and processed according to standard U.S. Geological Survey protocols. Samples are preserved onsite with 6N hydrochloric acid in a ratio of 1 to 100 in a borosilicateglass bottle with fluoropolymer-lined cap. Mercury species are oxidized to mercury (II) by using bromine monochloride; excess oxidation reagent is neutralized with hydroxylamine hydrochloride. Elemental mercury produced after adding stannous chloride is purged from the solution with ultrapure argon gas into a cell in which the mercury concentration is measured by atomic fluorescence emission at 253.7 nanometers. The analytical response is linear up to 125 nanograms per liter (ng/L) of mercury, and the short-term method detection limit is about 5 ng/L. The analytical variability at 50 ng/L is about 10 percent. This report describes the method and compares the use of hydrochloric acid to acid dichromate as a field preservative. Ambient mercury concentrations in hydrochloric acidpreserved samples stored in borosilicate-glass bottles with fluoropolymer-lined caps are shown to be stable for at least 30 days. Mercury concentrations are stable for at least 5 months after bromine monochloride is added to the sample bottles in the laboratory. The long-term average percent recoveries at 20, 45, and 75 ng/L in reagent water, filtered and unfiltered ground water, and filtered and unfiltered surface water range from 89 to 108, 96 to 103, and 94 to 98 percent, respectively.

Water-Resources Investigations Report

Methods of analysis by the U.S. Geological Survey National Water Quality Laboratory-Use of a modified ultrasonic nebulizer for the analysis of low ionic-strength water by inductively coupled optical emission spectrometry

The U.S. Geological Survey National Water Quality Laboratory has developed a method for the determination of dissolved calcium, iron, magnesium, manganese, silica, and sodium using a modified ultrasonic nebulizer sample-introduction system to an inductively coupled plasma-optical emission spectrometer. The nebulizer's spray chamber has been modified to avoid carryover and memory effects common in some conventional ultrasonic designs. The modified ultrasonic nebulizer is equipped with a high-speed rinse cycle to remove previously analyzed samples from the spray chamber without excessive flush times. This new rinse cycle decreases sample washout times by reducing carryover and memory effects from salt or analytes in previously analyzed samples by as much as 45 percent. Plasma instability has been reduced by repositioning the argon carrier gas inlet on the spray chamber and by directly pumping waste from the chamber, instead of from open drain traps, thereby maintaining constant pressure to the plasma. The ultrasonic nebulizer improves signal intensities, which are 8 to 16 times greater than for a conventional cross-flow pneumatic nebulizer, without being sensitive to clogging from salt buildup as in cross-flow nebulizers. Detection limits for the ultrasonic nebulizer are 4 to 18 times less than detection limits achievable using a cross-flow pneumatic nebulizer, with equivalent sample analysis time.

Open-File Report