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Title: Stability of metal ions in aqueous environmental samples

Conference · · Natl. Bur. Stand. (U.S.), Spec. Publ.; (United States)
OSTI ID:7230728

The time lapse between the collection of aqueous environmental samples and the analysis affects the original ionic concentration. Studies have proven the nonionic species in a water sample have more of an effect on the veracity of an analysis than the ''container wall'' effect, and that adjustment to a pH of 2 at sample collection time is a ''Pyrrhic victory.'' Lead, for example, will commonly increase an order of magnitude when unfiltered samples are adjusted to a pH of 2 upon collection. This effect is greatest when elemental ions are present in the ng ml/sup -1/ range and lessens as the original ionic concentration increases. Data are presented that behooves filtration of stream water and rainwater samples prior to any acidification step. The need to acidify the resulting filtrate is also discussed. Lithium, sodium, potassium, cesium, magnesium, calcium, strontium, manganese, iron, copper, silver, zinc, cadmium, aluminum, indium, and lead are examined. The insoluble phase retained on the filter can be digested with acid and also analyzed. The separate analysis of the filtrate and filter will give a true representation of the occurrence of these metals in nature. Flame and flameless atomic aborption and emission are used to perform the trace analyses.

Research Organization:
Illinois State Water Survey, Urbana
OSTI ID:
7230728
Journal Information:
Natl. Bur. Stand. (U.S.), Spec. Publ.; (United States), Vol. 1; Conference: 7. materials research symposium, Gaithersburg, MD, USA, 7 Oct 1974; Other Information: See NBS-SPEC.PUBL.--422(Vol.1); CONF-741023--P1
Country of Publication:
United States
Language:
English