Water load of uranium radium, and gross beta activity at selected gaging stations, water year 1960-61
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Geology topics
Publications and source records attributed to J. O. Johnson.
No abstract available.
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A method is described for the determination of very low concentrations of uranium in water. The method is based on the fluorescence of uranium in a pad prepared by fusion of the dried solids from the water sample with a flux of 10 percent NaF 45.5 percent Na2CO3 , and 45.5 percent K2CO3 . This flux permits use of a low fusion temperature and yields pads which are easily removed from the platinum fusion dishes for fluorescence measurements. Uranium concentrations of less than 1 microgram per liter can be determined on a sample of 10 milliliters, or less. The sensitivity and accuracy of the method are dependent primarily on the purity of reagents used, the stability and linearity of the fluorimeter, and the concentration of quenching elements in the water residue. A purification step is recommended when the fluorescence is quenched by more than 30 percent. Equations are given for the calculation of standard deviations of analyses by this method. Graphs of error functions and representative data are also included.
Radium isotopes are common radioactive constituents of natural waters. The concentration of radium-226 in potable water is of particular significance because this isotope is generally considered the most hazardous of all radionuclides with respect to ingestion. The approximate concentration of radium-226 is determined after coprecipitating radium with barium sulfate. The short-lived daughters of radium are allowed to grow for 10-12 days, then the alpha activity of the precipitate is measured and compared with that of a precipitate containing a known amount of radium-226. Concentrations of the individual alpha-emitting isotopes of radium-223, radium-224, and radium-226, are determined by coprecipitating radium first with lead sulfate, then with barium chloride, and finally with barium sulfate. This final precipitate is initially free of other alpha-emitting nuclides, thus permitting the isotopic composition to be determined by measuring the growth and decay of the alpha activity of the precipitate.