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F. B. Barker

Publications and source records attributed to F. B. Barker.

4 recordsLinked to original sources

Modified determination of radium in water

The proposed method embodies a barium sulfate carrier precipitation, filtration through molecular filter membranes, and collection of activity after prescribed aging period. The method is sufficiently accurate and precise to indicate the potability of water and for use in general studies of radium in chemical hydrology. Amounts of radium as low as 0.1 μ μ c. can be detected by using 1 -hour counting times. Radium-226 is used as the standard and the results indicate about 100 to 110 % of the activity of the alpha-emitting radium isotopes as radium-223, radium-224, and radium-226.

Analytical Chemistry

Determination of uranium in natural waters

The fluorophotometric determination of uranium was studied to develop a procedure applicable to the routine analysis of waters. Three grams of the high carbonate flux are used in a dilution procedure with spiking. Because of the comparatively high reflectivity of this large disk and the low uranium concentration, a correction for nonquenched light is required. A formula is developed to compensate for the effect, an electrical fusion device is described, and the problem of fixing uranium in waters is discussed.

Analytical Chemistry

Determination of beta activity in water

Many elements have one or more naturally radioactive isotopes, and several hundred other radionuclides have been produced artificially. Radioactive substances may be present in natural water as a result of geochemical processes or the release of radioactive waste and other nuclear debris to the environment. The Geological Survey has developed methods for measuring certain of these .radioactive substances in water. Radioactive substances often are present in water samples in microgram quantities or less. Therefore, precautions must be taken to prevent loss of material and to assure that the sample truly represents its source at the time of collection. Addition of acids, complexing agents, or stable isotopes often aids in preventing loss of radioactivity on container walls, on sediment, or on other solid materials in contact with the sample. The disintegration of radioactive atoms is a random process subject to established methods of statistical analysis. Because many water samples contain small amounts of radioactivity, low-level counting techniques must be used. The usual assumption that counting data follow a Gaussian distribution is invalid under these conditions, and statistical analyses must be based on the Poisson distribution. The gross beta activity in water samples is determined from the residue left after evaporation of the sample to dryness. Evaporation is accomplished first in a teflon dish, then the residue is transferred with distilled water to a counting planchet and again is reduced to dryness. The radioactivity on the planchet is measured with an anticoincidence-shielded, low-background, beta counter and is compared with measurements of a strontium-90-yttrium-90 standard prepared and measured in the same manner. Control charts are used to assure consistent operation of the counting instrument.

Water Supply Paper

Data on uranium and radium in ground water in the United States, 1954 to 1957

This report is one of a series resulting from a study by the U.S. Geological Survey to determine the occurrence and distribution of naturally radioactive substances in water. From 1954-57 uranium and radium concentrations were determined in 561 samples, mainly of ground water, having wide geologic and geographic distribution. These concentrations, together with data on the hydrologic and geologic environment, the beta-gamma activity, and the chemical characteristics of each sample, are tabulated by States. The conterminous United States was subdivided into 10 geotectonic regions to facilitate statistical interpretation of the occurrence of uranium and radium in fresh water in approximately homogeneous geologic provinces. For each geotectonic region, the range and median were determined for the concentrations of radium and uranium; for regions from which sufficient data were available, log-normal frequency distribution curves were calculated and superimposed on histograms of radium and uranium concentrations in the samples. An "anomaly threshold" is suggested for both radioelements for each region analyzed statistically. The western stable region had the greatest median and highest "anomaly threshold" for uranium. This region also had the highest "anomaly threshold" for radium, but the largest median for radium was found for samples collected in the Ozark-Ouachita system. The median concentration for uranium was lowest for the Atlantic and Gulf Coastal Plain and the Pacific orogenic belt. This latter region also had the lowest median-radium content.

Professional Paper