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Hugh T. Millard

Publications and source records attributed to Hugh T. Millard.

21 records · Page 2Linked to original sources

Osmium, ruthenium, iridium and uranium in silicates and chromite from the eastern Bushveld Complex, South Africa

Osmium, ruthenium, iridium and uranium contents were determined in eight ortho pyroxene, seven plagioclase, and three chromite mineral separates from the eastern Bushveld Complex. Neutron activation analysis was used to measure the platinum metals, and uranium was determined by a fission track technique. The platinum metals were found to be present within each minéral in the proportions Os : Ru : Ir = 1:7:1, while the concentrations of these metals in the minerals are in the ratios orthopyroxene:plagioclase:chromite = 1:16:700. The concentration of uranium was found to range from 11 to 66 ppb (parts per billion) and not to vary significantly from mineral to mineral. The data for the platinum metals are consistent with a model in which the eastern Bushveld Complex was formed by the fractional crystallization of two separately injected magmas. A computer fit of this model to these data indicates that the initial concentrations of Os, Ru and Ir in the first magma were 0.24, 2.0 and 0.21 ppb and in the second magma were 0.16, 1.1 and 0.18 ppb, respectively. The fit also yields the distribution coefficients for the partitioning between the liquid and cumulus orthopyroxene, cumulus plagioclase and cumulus chromite. These coefficients (mineral/liquid) for osmium are 4.5, 66 and 2700; for ruthenium, they are 5, 65 and 2700; and for iridium, they are 4, 60 and 1600. To make this fit, it was necessary to hypothesize the existence of two types of chromite: one type with a large distribution coefficient, presumably formed as a cumulus phase at high temperature, and another, more prevalent type with a smaller distribution coefficient, which may have been formed by postcumulus growth at a lower temperature. This hypothesis is supported by data for coexisting chromite-silicate pairs, which indicate that the chromite grains expelled these platinum metals as they cooled.

Geochimica et Cosmochimica Acta↗

A neutron activation analysis procedure for the determination of uranium, thorium and potassium in geologic samples

A neutron activation analysis procedure was developed for the determination of uranium, thorium and potassium in basic and ultrabasic rocks. The three elements are determined in the same 0.5-g sample following a 30-min irradiation in a thermal neutron flux of 2·10 12 n·cm −2 ·sec −1 . Following radiochemical separation, the nuclides 239 U (T=23.5 m), 233 Th (T=22.2 m) and 42 K (T=12.36 h) are measured by β-counting. A computer program is used to resolve the decay curves which are complex owing to contamination and the growth of daughter activities. The method was used to determine uranium, throium and potassium in the U. S. Geological Survey standard rocks DTS-1, PCC-1 and BCR-1. For 0.5-g samples the limits of detection for uranium, throium and potassium are 0.7, 1.0 and 10 ppb, respectively.

Journal of Radioanalytical Chemistry↗

Establishment of gold-quartz standard GQS-1

A homogeneous gold-quartz standard, GQS-1, was prepared from a heterogeneous gold-bearing quartz by chemical treatment. The concentration of gold in GQS-1 was determined by both instrumental neutron activation analysis and radioisotope dilution analysis to be 2.61?0.10 parts per million. Analysis of 10 samples of the standard by both instrumental neutron activation analysis and radioisotope dilution analysis failed to reveal heterogeneity within the standard. The precision of the analytical methods, expressed as standard error, was approximately 0.1 part per million. The analytical data were also used to estimate the average size of gold particles. The chemical treatment apparently reduced the average diameter of the gold particles by at least an order of magnitude and increased the concentration of gold grains by a factor of at least 4,000.

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